Corrosion and Corrosion Control, 4th Ed

CORROSION AND
CORROSION CONTROL
An Introduction
to Corrosion Science
and Engineering
FOURTH EDITION
R. Winston Revie
Senior Research Scientist
CANMET Materials Technology Laboratory
Natural Resources Canada
Herbert H. Uhlig
Former Professor Emeritus
Department of Materials Science and Engineering
Massachusetts Institute of Technology
A JOHN WILEY & SONS, INC., PUBLICATION

CORROSION AND
CORROSION CONTROL
CORROSION AND
CORROSION CONTROL
An Introduction
to Corrosion Science
and Engineering
FOURTH EDITION
R. Winston Revie
Senior Research Scientist
CANMET Materials Technology Laboratory
Natural Resources Canada
Herbert H. Uhlig
Former Professor Emeritus
Department of Materials Science and Engineering
Massachusetts Institute of Technology
A JOHN WILEY & SONS, INC., PUBLICATION

Copyright © 2008 by John Wiley & Sons, Inc. All right reserved
Published by John Wiley & Sons, Inc., Hoboken New Jersey

Published simultaneously in Canada
No part of this publication may be reproduced, stored in a retrieval system, or transmitted in any
form or by any means, electronic, mechanical, photocopying, recording, scanning, or otherwise,
except as permitted under Section 107 or 108 of the 1976 United States Copyright Act, without
either the prior written permission of the Publisher, or authorization through payment of the
appropriate per-copy fee to the Copyright Clearance Center, Inc., 222 Rosewood Drive, Danvers,
MA 01923, (978) 750-8400, fax (978)750-4470, or on the web at www.copyright.com. Requests to
the Publisher for permission should be addressed to the Permissions Department, John Wiley &
Sons, Inc., 111 River Street, Hoboken, NJ 07030, (201) 748-6011, fax (201) 748-6008, or online at
http://www.wiley.com/go/permission.
Limit of Liability/Disclaimer of Warranty: While the publisher and author have used their best
efforts in preparing this book, they make no representations or warranties with respect to the
accuracy or completeness of the contents of this book and specifically disclaim any implied
warranties of merchantability or fitness for a particular purpose. No warranty may be created or
extended by sales representatives or written sales materials. The advice and strategies contained
herein may not be suitable for your situation. You should consult with a professional where
appropriate. Neither the publisher nor author shall be liable for any loss of profit or any other
commercial damages, including but not limited to special, incidental, consequential, or other
damages.
For general information on our other products and services or for technical support, please contact
our Customer Care Department within the United States at (800) 762-2974, outside the United
States at (317) 572-3993 or fax (317) 572-4002.
Wiley also publishes its books in a variety of electronic formats. Some content that appears in print
may not be available in electronic formats. For more information about Wiley products, visit our
web site at www.wiley.com.
Library of Congress Cataloging-in-Publication Data:
Uhlig, Herbert Henry, 1907–

Corrosion and corrosion control : an introduction to corrosion science and engineering /
Herbert H. Uhlig, R. Winston Revie.—4th ed.
p. cm.
Includes bibliographical references and index.
ISBN 978-0-471-73279-2 (cloth)
1. Corrosion and anti-corrosives. I. Revie, R. Winston (Robert Winston), 1944– II. Title.
TA462.U39 2008
620.1′1223–dc22
2007041578
Printed in the United States of America
10 9 8 7 6 5 4 3 2 1
CONTENTS
Preface xvii
1 DEFINITION AND IMPORTANCE OF CORROSION 1

1.1 Definition of Corrosion 1
1.1.1 Corrosion Science and Corrosion Engineering 1
1.2 Importance of Corrosion 2
1.3 Risk Management 5
1.4 Causes of Corrosion 6
1.4.1 Change in Gibbs Free Energy 6
1.4.2 Pilling–Bedworth Ratio 6
References 6
General References 7
Problems 7
2 ELECTROCHEMICAL MECHANISMS 9
2.1 The Dry-Cell Analogy and Faraday’s Law 9
2.2 Definition of Anode and Cathode 11
2.3 Types of Cells 13
2.4 Types of Corrosion Damage 15
References 18
Problems 19
3 THERMODYNAMICS: CORROSION TENDENCY AND

ELECTRODE POTENTIALS 21
3.1 Change of Gibbs Free Energy 21
3.2 Measuring the Emf of a Cell 22
3.3 Calculating the Half-Cell Potential—The Nernst Equation 22
3.4 The Hydrogen Electrode and the Standard Hydrogen Scale 24
3.5 Convention of Signs and Calculation of Emf 25
v
vi CONTENTS
3.6 Measurement of pH 28
3.7 The Oxygen Electrode and Differential Aeration Cell 28
3.8 The Emf and Galvanic Series 30
3.9 Liquid Junction Potentials 33
3.10 Reference Electrodes 34
3.10.1 Calomel Reference Electrode 35
3.10.2 Silver–Silver Chloride Reference Electrode 36
3.10.3 Saturated Copper–Copper Sulfate Reference
Electrode 36
References 37
Problems 38
Answers to Problems 40
4 THERMODYNAMICS: POURBAIX DIAGRAMS 43

4.1 Basis of Pourbaix Diagrams 43
4.2 Pourbaix Diagram for Water 44
4.3 Pourbaix Diagram for Iron 45
4.4 Pourbaix Diagram for Aluminum 47
4.5 Pourbaix Diagram for Magnesium 48
4.6 Limitations of Pourbaix Diagrams 49
References 50
Problems 50
Answers to Problem 51
5 KINETICS: POLARIZATION AND CORROSION RATES 53

5.1 Polarization 53
5.2 The Polarized Cell 54
5.3 How Polarization Is Measured 56
5.3.1 Calculation of IR Drop in an Electrolyte 58
5.4 Causes of Polarization 58
5.5 Hydrogen Overpotential 63
5.6 Polarization Diagrams of Corroding Metals 66
5.7 Influence of Polarization on Corrosion Rate 68
5.8 Calculation of Corrosion Rates from Polarization Data 71
5.9 Anode–Cathode Area Ratio 73
5.10 Electrochemical Impedance Spectroscopy 75
CONTENTS vii
5.11 Theory of Cathodic Protection 77

References 79
Problems 80
6 PASSIVITY 83
6.1 Definition 83
6.2 Characteristics of Passivation and the Flade Potential 84
6.3 Behavior of Passivators 88
6.3.1 Passivation of Iron by HNO3 89
6.4 Anodic Protection and Transpassivity 90
6.5 Theories of Passivity 92
6.5.1 More Stable Passive Films with Time 95
6.5.2 Action of Chloride Ions and Passive–Active Cells 96
6.6 Critical Pitting Potential 97
6.7 Critical Pitting Temperature 99
6.8 Passivity of Alloys 100
6.8.1 Nickel–Copper Alloys 103
6.8.2 Other Alloys 108
6.9 Effect of Cathodic Polarization and Catalysis 108
References 109
Problems 112
7 IRON AND STEEL 115

7.1 Introduction 115
7.2 Aqueous Environments 116
7.2.1 Effect of Dissolved Oxygen 116
7.2.2 Effect of Temperature 120
7.2.3 Effect of pH 120
7.2.4 Effect of Galvanic Coupling 127
7.2.5 Effect of Velocity on Corrosion in Natural Waters 129
7.2.6 Effect of Dissolved Salts 131
7.3 Metallurgical Factors 138
7.3.1 Varieties of Iron and Steel 138
7.3.2 Effects of Composition 138
viii CONTENTS
7.3.3 Effect of Heat Treatment 142

7.4 Steel Reinforcements in Concrete 143
References 145
Problems 147
8 EFFECT OF STRESS 149

8.1 Cold Working 149
8.2 Stress-Corrosion Cracking 150
8.2.1 Iron and Steel 151
8.3 Mechanism of Stress-Corrosion Cracking of Steel and
Other Metals 156
8.3.1 Electrochemical Dissolution 157
8.3.2 Film-Induced Cleavage 158
8.3.3 Adsorption-Induced Localized Slip 158
8.3.4 Stress Sorption 158
8.3.5 Initiation of Stress-Corrosion Cracking and
Critical Potentials 161
8.3.6 Rate of Crack Growth (Fracture Mechanics) 162
8.4 Hydrogen Damage 166
8.4.1 Mechanism of Hydrogen Damage 167
8.4.2 Effect of Metal Flaws 170
8.5 Radiation Damage 172
8.6 Corrosion Fatigue 173
8.6.1 Critical Minimum Corrosion Rates 177
8.6.2 Remedial Measures 178
8.6.3 Mechanism of Corrosion Fatigue 179
8.7 Fretting Corrosion 180
8.7.1 Mechanism of Fretting Corrosion 182
8.7.2 Remedial Measures 184
References 185
Problems 190
9 ATMOSPHERIC CORROSION 191

9.2 Types of Atmospheres 192
CONTENTS ix
9.3 Corrosion-Product Films 192

9.4 Factors Influencing Corrosivity of the Atmosphere 195
9.4.1 Particulate Matter 196
9.4.2 Gases in the Atmosphere 197
9.4.3 Moisture (Critical Humidity) 199
9.5 Remedial Measures 201
References 202
Problems 204
10 CORROSION IN SOILS 205

10.2 Factors Affecting the Corrosivity of Soils 206
10.3 Bureau of Standards Tests 207
10.3.1 Pitting Characteristics 208
10.4 Stress-Corrosion Cracking 210
10.5 Remedial Measures 211
References 212
11 OXIDATION 215
11.2 Initial Stages 216
11.3 Thermodynamics of Oxidation: Free
Energy–Temperature Diagram 218
11.4 Protective and Nonprotective Scales 218
11.4.1 Three Equations of Oxidation 220
11.5 Wagner Theory of Oxidation 223
11.6 Oxide Properties and Oxidation 224
11.7 Galvanic Effects and Electrolysis of Oxides 227
11.8 Hot Ash Corrosion 229
11.9 Hot Corrosion 229
11.10 Oxidation of Copper 230
11.10.1 Internal Oxidation 231
11.10.2 Reaction with Hydrogen (“Hydrogen Disease”) 231
11.11 Oxidation of Iron and Iron Alloys 232
11.12 Life Test for Oxidation-Resistant Wires 233
11.13 Oxidation-Resistant Alloys 234
11.13.1 Reactive Element Effect (REE) 234
x CONTENTS
11.13.2 Chromium–Iron Alloys 235

11.13.3 Chromium–Aluminum–Iron Alloys 236
11.13.4 Nickel and Nickel Alloys 236
11.13.5 Furnace Windings 237
References 237
Problems 239
12 STRAY-CURRENT CORROSION 241

12.2 Sources of Stray Currents 242
12.3 Quantitative Damage by Stray Currents 244
12.4 Detection of Stray Currents 245
12.5 Soil-Resistivity Measurement 246
12.6 Means for Reducing Stray-Current Corrosion 246
References 247
Problems 247
13 CATHODIC PROTECTION 251

13.2 Brief History 252
13.3 How Applied 253
13.3.1 Sacrificial Anodes 254
13.4 Combined Use with Coatings 255
13.5 Magnitude of Current Required 257
13.6 Anode Materials and Backfill 258
13.6.1 Overprotection 259
13.7 Criteria of Protection 260
13.7.1 Potential Measurements 260
13.7.2 Doubtful Criteria 262
13.7.3 Position of Reference Electrode 262
13.8 Economics of Cathodic Protection 263
13.9 Anodic Protection 263
References 265
CONTENTS xi
Problems 266
14 METALLIC COATINGS 269

14.1 Methods of Application 269
14.2 Classification of Coatings 271
14.3 Specific Metal Coatings 272
14.3.1 Nickel Coatings 272
14.3.2 Lead Coatings 274
14.3.3 Zinc Coatings 274
14.3.4 Cadmium Coatings 276
14.3.5 Tin Coatings 277
14.3.6 Chromium-Plated Steel for Containers 279
14.3.7 Aluminum Coatings 280
References 281
15 INORGANIC COATINGS 285

15.1 Vitreous Enamels 285
15.2 Portland Cement Coatings 286
15.3 Chemical Conversion Coatings 286
References 288
16 ORGANIC COATINGS 289

16.2 Paints 289
16.3 Requirements for Corrosion Protection 291
16.4 Metal Surface Preparation 293
16.4.1 Cleaning All Dirt, Oils, and Greases from
the Surface 293
16.4.2 Complete Removal of Rust and Mill Scale 294
16.5 Applying Paint Coatings 295
16.5.1 Wash Primer 296
16.5.2 Painting of Aluminum and Zinc 296
16.6 Filiform Corrosion 296
16.6.1 Theory of Filiform Corrosion 298
16.7 Plastic Linings 299
xii CONTENTS
References 300
17 INHIBITORS AND PASSIVATORS 303

17.2 Passivators 304
17.2.1 Mechanism of Passivation 304
17.2.2 Applications of Passivators 308
17.3 Pickling Inhibitors 310
17.3.1 Applications of Pickling Inhibitors 312
17.4 Slushing Compounds 313
17.5 Vapor-Phase Inhibitors 313
17.5.1 Inhibitor to Reduce Tarnishing of Copper 314
References 315
18 TREATMENT OF WATER AND STEAM SYSTEMS 317

18.1 Deaeration and Deactivation 317
18.2 Hot- and Cold-Water Treatment 321
18.2.1 Cooling Waters 322
18.3 Boiler-Water Treatment 323
18.3.1 Boiler Corrosion 323
18.3.2 Boiler-Water Treatment for Corrosion Control 326
18.3.3 Mechanisms 328
References 330
19 ALLOYING FOR CORROSION RESISTANCE;

STAINLESS STEELS 333
19.2 Stainless Steels 335
19.2.1 Brief History 336
19.2.2 Classes and Types 337
19.2.3 Intergranular Corrosion 343
19.2.4 Pitting and Crevice Corrosion 350
19.2.5 Stress-Corrosion Cracking and Hydrogen Cracking 354
19.2.6 Cracking of Sensitized Austenitic Alloys in
Polythionic Acids 359
CONTENTS xiii
19.2.7 Galvanic Coupling and General Corrosion

Resistance 361
References 362
20 COPPER AND COPPER ALLOYS 367

20.1 Copper 367
20.1.1 Corrosion in Natural Waters 369
20.2 Copper Alloys 371
20.2.1 Copper–Zinc Alloys (Brasses) 371
20.2.2 Dealloying/Dezincification 372
20.2.3 Stress-Corrosion Cracking (Season Cracking) 374
20.2.4 Condenser Tube Alloys Including
Copper–Nickel Alloys 378
References 379
Problems 381
21 ALUMINUM AND ALUMINUM ALLOYS 383

21.1 Aluminum 383
21.1.1 Clad Alloys 384
21.1.2 Corrosion in Water and Steam 384
21.1.3 Effect of pH 387
21.1.4 Corrosion Characteristics 388
21.1.5 Galvanic Coupling 392
21.2 Aluminum Alloys 393
21.2.1 Stress-Corrosion Cracking 394
References 396
22 MAGNESIUM AND MAGNESIUM ALLOYS 399

22.2 Magnesium 399
22.3 Magnesium Alloys 400
22.3.1 Stress-Corrosion Cracking 402
22.3.2 Coatings 403
22.4 Summary 404
xiv CONTENTS
References 405
23 NICKEL AND NICKEL ALLOYS 407

23.2 Nickel 408
23.3 Nickel Alloys 411
23.3.1 General Behavior 411
23.3.2 Ni–Cu System: Alloy 400—70% Ni, 30% Cu 414
23.3.3 Ni–Cr–Fe System: Alloy 600—76% Ni, 16% Cr,
7% Fe 414
23.3.4 Ni–Mo System: Alloy B—60% Ni, 30% Mo,
5% Fe 415
23.3.5 Ni–Cr–Fe–Mo–Cu System: Alloy G—Ni, 22%
Cr, 20% Fe, 6.5% Mo, 2% Cu 416
23.3.6 Ni–Cr–Mo System: Alloy C—54% Ni, 15% Cr,
16% Mo, 4% W, 5% Fe 416
23.3.7 Ni–Fe–Cr System: Alloy 825—Ni, 31% Fe, 22% Cr 417
References 417
24 COBALT AND COBALT ALLOYS 419

24.2 Cobalt Alloys 420
References 423
25 TITANIUM 425
25.1 Titanium 425
25.2 Titanium Alloys 427
25.3 Pitting and Crevice Corrosion 429
25.4 Intergranular Corrosion and Stress-Corrosion Cracking 430
References 432
Problem 434
26 ZIRCONIUM 435
26.2 Zirconium Alloys 436
CONTENTS xv
26.3 Behavior in Hot Water and Steam 437

References 439
27 TANTALUM 441
27.2 Corrosion Behavior 441
References 443
General Reference 443
28 LEAD 445
28.2 Corrosion Behavior of Lead and Lead Alloys 446
28.2.1 Lead–Acid Battery 447
28.3 Summary 448
References 449
29 APPENDIX 451
29.1 Activity and Activity Coefficients of Strong
Electrolytes 451
29.2 Derivation of Stern–Geary Equation for Calculating
Corrosion Rates from Polarization Data Obtained at
Low Current Densities 456
29.2.1 The General Equation 458
29.3 Derivation of Equation Expressing the Saturation Index
of a Natural Water 461
29.4 Derivation of Potential Change along a Cathodically
Protected Pipeline 467
29.5 Derivation of the Equation for Potential Drop along
the Soil Surface Created by Current Entering or
Leaving a Buried Pipe 469
29.6 Derivation of the Equation for Determining Resistivity
of Soil by Four-Electrode Method 470
29.7 Derivation of the Equation Expressing Weight Loss by
Fretting Corrosion 471
29.8 Conversion Factors 474
29.8.1 Additional Conversion Factors 475
29.8.2 Current Density Equivalent to a Corrosion Rate
of 1 gmd 475
xvi CONTENTS
29.9 Standard Potentials 476

29.10 Notation and Abbreviations 476
References 478
Index 479
PREFACE
The three main global challenges for the twenty-first century are energy, water,
and air—that is, sufficient energy to ensure a reasonable standard of living,
clean water to drink, and clean air to breathe. The ability to manage corrosion
is a central part of using materials effectively and efficiently to meet these
challenges. For example, oil and natural gas are transmitted across continents
using high-pressure steel pipelines that must operate for decades without
failure, so that neither the groundwater nor the air is unnecessarily polluted.
In design, operation, and maintenance of nuclear power plants, management
of corrosion is critical. The reliability of materials used in nuclear waste dis-
posal must be sufficient so that that the safety of future generations is not
compromised.
Materials reliability is becoming ever more important in our society, particu-
larly in view of the liability issues that develop when reliability is not assured,
safety is compromised, and failure occurs. Notwithstanding the many years over
which university, college, and continuing education courses in corrosion have
been available, high-profile corrosion failures continue to take place. Although
the teaching of corrosion should not be regarded as a dismal failure, it has cer-
tainly not been a stellar success providing all engineers and technologists a basic
minimum “literacy level” in corrosion that would be sufficient to ensure reliabil-
ity and prevent failures.
Senior management of some organizations has adopted a policy of “zero
failures” or “no failures.” In translating this management policy into reality, so
that “zero” really does mean “zero” and “no” means “no,” engineers and others
manage corrosion using a combination of well-established strategies, innovative
approaches, and, when necessary, experimental trials.
One objective of preparing the fourth edition of this book is to present to
students an updated overview of the essential aspects of corrosion science and
engineering that underpin the tools that are available and the technologies that
are used for managing corrosion and preventing failures. A second objective is
to engage students, so that they are active participants in understanding corrosion
and solving problems, rather than passively observing the smorgasbord of infor-
mation presented. The main emphasis is on quantitative presentation, explana-
tion, and analysis wherever possible; for example, in this new edition, the galvanic
series in seawater is presented with the potential range of each material, rather
than only as a qualitative list. Considering the potential ranges that can be
involved, the student can see how anodic/cathodic effects can develop, not only
xvii
xviii PREFACE
when different materials form a couple, but also when materials that are nomi-
nally the same are coupled. In this edition, some new numerical problems have
been added, and the problems are integrated into the book by presenting them
at the ends of the chapters.
Since the third edition of this book was published, there have been many
advances in corrosion, including advances in knowledge, advances in alloys for
application in aggressive environments, and advances of industry in response to
public demand. For example, consumer demand for corrosion protection of auto-
mobiles has led to a revolution of materials usage in the automotive industry. For
this reason, and also because many students have a fascination with cars, numer-
ous examples throughout this book illustrate advances that have been made in
corrosion engineering of automobiles. Advances in protecting cars and trucks
from corrosion must also be viewed in the context of reducing vehicle weight by
using magnesium, aluminum, and other lightweight materials in order to decrease
energy usage (increase the miles per gallon, or kilometers per liter, of gasoline)
and reduce greenhouse gas emissions.
Although the basic organization of the book is unchanged from the previous
edition, there is in this edition a separate chapter on Pourbaix diagrams, very
useful tools that indicate the thermodynamic potential–pH domains of corrosion,
passivity, and immunity to corrosion. A consideration of the relevant Pourbaix
diagrams can be a useful starting point in many corrosion studies and investiga-
tions. As always in corrosion, as well as in this book, there is the dual importance
of thermodynamics (In which direction does the reaction go? Chapters 3 and 4)
and kinetics (How fast does it go? Chapter 5).
After establishing the essential basics of corrosion in the first five chapters,
the next 23 chapters expand upon the fundamentals in specific systems and appli-
cations and discuss strategies for protection. There are separate chapters on alu-
minum (Chapter 21), magnesium (Chapter 22), and titanium (Chapter 25) to
provide more information on these metals and their alloys than in the previous
editions. Throughout this book, environmental concerns and regulations are pre-
sented in the context of their impact on corrosion and its control—for example,
the EPA Lead and Copper rule enacted in the United States in 1991. The indus-
trial developments in response to the Clean Air Act, enacted in 1970, have
reduced air pollution in the United States, with some effect on atmospheric cor-
rosion (Chapter 9). To meet the requirements of environmental regulations and
reduce the use of organic solvents, compliant coatings have been developed
(Chapter 16).
This is primarily a textbook for students and others who need a basic under-
standing of corrosion. The book is also a reference and starting point for engi-
neers, researchers, and technologists requiring specific information. The book
includes discussion of the main materials that are available, including alloys both
old and new. For consistency with current practice in metallurgical and engineer-
ing literature, alloys are identified with their UNS numbers as well as with their
commonly used identifiers. To answer the question from students about why so
PREFACE xix
many alloys have been developed and are commercially available, the contribu-
tions of individual elements to endow alloys with unique properties that are
valuable for specific applications are discussed. Throughout the book, there are
numerous references to further sources of information, including handbooks,
other books, reviews, and papers in journals. At the end of each chapter, there is
a list of “General References” pertinent to that chapter, and most of these were
published in 2000 and later.
This edition includes introductory discussions of risk (Chapter 1), AC imped-
ance measurements (Chapter 5), Ellingham diagrams (Chapter 11), and, through-
out the book, discussions of new alloys that have been developed to meet demands
for increasing reliability notwithstanding the increased structural lifetimes that are
being required in corrosive environments of ever-increasing severity. Perhaps
nowhere are the demands for reliability more challenging than in nuclear reactors,
discussed in Chapters 8 and 26. In the discussion of stainless steels (Chapter 19),
the concept of critical pitting temperature (CPT) is introduced, as well as the infor-
mation on critical pitting potential (CPP). The important problem of corrosion of
rebar (reinforced steel in concrete) is discussed in Chapter 7 on iron and steel.
In addition to new technologies and new materials for managing corrosion,
new tools for presenting books have become available; hence, this book is being
published as an electronic book, as well as in the traditional print format. An
instructor’s manual is also being prepared.
Experience has been invaluable in using the book in a corrosion course in
the Department of Mechanical and Aerospace Engineering at Carleton Univer-
sity in Ottawa, which Glenn McRae and I developed along with other members
of the Canadian National Capital Section of NACE International.
It would be a delight for me to hear from readers of this book, with their
suggestions and ideas for future editions.
I would like to acknowledge my many friends and colleagues at the CANMET
Materials Technology Laboratory, with whom it has been my privilege to work
for the past nearly 30 years. I would also like to thank the many organizations
and individuals who have granted permission to use copyright material; acknowl-
edgments for specific material are provided throughout the book. In addition,
I would like to thank Bob Esposito and his staff at John Wiley & Sons, Inc.
for their encouragement with this book and also with the Wiley Series in
Corrosion.
I would like to thank the Uhlig family for their generosity and hospitality
during five decades, beginning when I was a student in the M.I.T. Corrosion
Laboratory in the 1960s and 1970s. In particular, I would like to acknowledge
Mrs. Greta Uhlig, who continues to encourage initiatives in corrosion education
in memory of the late Professor Herbert H. Uhlig (1907–1993).
Lastly, I would like to quote from the Preface of the first edition of this book:
If this book stimulates young minds to accept the challenge of continuing corrosion
problems, and to help reduce the huge economic losses and dismaying wastage of
xx PREFACE
natural resources caused by metal deterioration, it will have fulfilled the author’s
major objective.
Indeed, this remains the main objective today.
Ottawa, Canada R. Winston Revie

September 2007
1
DEFINITION AND IMPORTANCE
OF CORROSION
1.1 DEFINITION OF CORROSION
Corrosion is the destructive attack of a metal by chemical or electrochemical

reaction with its environment. Deterioration by physical causes is not called cor-
rosion, but is described as erosion, galling, or wear. In some instances, chemical
attack accompanies physical deterioration, as described by the following terms:
corrosion–erosion, corrosive wear, or fretting corrosion. Nonmetals are not
included in this definition of corrosion. Plastics may swell or crack, wood may
split or decay, granite may erode, and Portland cement may leach away, but the
term corrosion, in this book, is restricted to chemical attack of metals.
“Rusting” applies to the corrosion of iron or iron-base alloys with formation
of corrosion products consisting largely of hydrous ferric oxides. Nonferrous
metals, therefore, corrode, but do not rust.
1.1.1 Corrosion Science and Corrosion Engineering

Since corrosion involves chemical change, the student must be familiar with
principles of chemistry in order to understand corrosion reactions. Because
corrosion processes are mostly electrochemical, an understanding of
Corrosion and Corrosion Control, by R. Winston Revie and Herbert H. Uhlig

Copyright © 2008 John Wiley & Sons, Inc.
1
2 DEFINITION AND IMPORTANCE OF CORROSION
electrochemistry is also important. Furthermore, since structure and composition

of a metal often determine corrosion behavior, the student should be familiar
with the fundamentals of physical metallurgy as well.
The corrosion scientist studies corrosion mechanisms to improve (a) the
understanding of the causes of corrosion and (b) the ways to prevent or at least
minimize damage caused by corrosion. The corrosion engineer, on the other hand,
applies scientific knowledge to control corrosion. For example, the corrosion
engineer uses cathodic protection on a large scale to prevent corrosion of buried
pipelines, tests and develops new and better paints, prescribes proper dosage of
corrosion inhibitors, or recommends the correct coating. The corrosion scientist,
in turn, develops better criteria of cathodic protection, outlines the molecular
structure of chemical compounds that behave best as inhibitors, synthesizes
corrosion-resistant alloys, and recommends heat treatment and compositional
variations of alloys that will improve their performance. Both the scientific and
engineering viewpoints supplement each other in the diagnosis of corrosion
damage and in the prescription of remedies.
1.2 IMPORTANCE OF CORROSION
The three main reasons for the importance of corrosion are: economics, safety,
and conservation. To reduce the economic impact of corrosion, corrosion engi-
neers, with the support of corrosion scientists, aim to reduce material losses, as
well as the accompanying economic losses, that result from the corrosion of
piping, tanks, metal components of machines, ships, bridges, marine structures,
and so on. Corrosion can compromise the safety of operating equipment by
causing failure (with catastrophic consequences) of, for example, pressure vessels,
boilers, metallic containers for toxic chemicals, turbine blades and rotors, bridges,
airplane components, and automotive steering mechanisms. Safety is a critical
consideration in the design of equipment for nuclear power plants and for dis-
posal of nuclear wastes. Loss of metal by corrosion is a waste not only of the
metal, but also of the energy, the water, and the human effort that was used to
produce and fabricate the metal structures in the first place. In addition, rebuild-
ing corroded equipment requires further investment of all these resources—
metal, energy, water, and human.
Economic losses are divided into (1) direct losses and (2) indirect losses.
Direct losses include the costs of replacing corroded structures and machinery
or their components, such as condenser tubes, mufflers, pipelines, and metal
roofing, including necessary labor. Other examples are (a) repainting structures
where prevention of rusting is the prime objective and (b) the capital costs plus
maintenance of cathodic protection systems for underground pipelines. Sizable
direct losses are illustrated by the necessity to replace several million domestic
hot-water tanks each year because of failure by corrosion and the need for
replacement of millions of corroded automobile mufflers. Direct losses include
the extra cost of using corrosion-resistant metals and alloys instead of carbon
IMPORTANCE OF CORROSION 3
steel where the latter has adequate mechanical properties but not sufficient cor-
rosion resistance; there are also the costs of galvanizing or nickel plating of steel,
of adding corrosion inhibitors to water, and of dehumidifying storage rooms for
metal equipment.
The economic factor is a very important motivation for much of the current
research in corrosion. Losses sustained by industry and by governments amount
to many billions of dollars annually, approximately $276 billion in the United
States, or 3.1% of the Gross Domestic Product (GDP), according to a recent
study [1]. It has been estimated that about 25–30% of this total could be avoided
if currently available corrosion technology were effectively applied [1].
Studies of the cost of corrosion to Australia, Great Britain, Japan, and other
countries have also been carried out. In each country studied, the cost of corro-
sion is approximately 3–4 % of the Gross National Product [2].
Indirect losses are more difficult to assess, but a brief survey of typical losses
of this kind compels the conclusion that they add several billion dollars to the
direct losses already outlined. Examples of indirect losses are as follows:
1. Shutdown. The replacement of a corroded tube in an oil refinery may cost

a few hundred dollars, but shutdown of the unit while repairs are under-
way may cost $50,000 or more per hour in lost production. Similarly,
replacement of corroded boiler or condenser tubes in a large power plant
may require $1,000,000 or more per day for power purchased from inter-
connected electric systems to supply customers while the boiler is down.
Losses of this kind cost the electrical utilities in the United States tens of
millions of dollars annually.
2. Loss of Product. Losses of oil, gas, or water occur through a corroded-
pipe system until repairs are made. Antifreeze may be lost through a cor-
roded auto radiator; or gas leaking from a corroded pipe may enter the
basement of a building, causing an explosion.
3. Loss of Efficiency. Loss of efficiency may occur because of diminished
heat transfer through accumulated corrosion products, or because of the
clogging of pipes with rust necessitating increased pumping capacity. It has
been estimated that, in the United States, increased pumping capacity,
made necessary by partial clogging of water mains with rust, costs many
millions of dollars per year. A further example is provided by internal-
combustion engines of automobiles where piston rings and cylinder walls
are continuously corroded by combustion gases and condensates. Loss of
critical dimensions leading to excess gasoline and oil consumption can be
caused by corrosion to an extent equal to or greater than that caused by
wear. Corrosion processes can impose limits on the efficiencies of energy
conversion systems, representing losses that may amount to billions of
dollars.
4. Contamination of Product. A small amount of copper picked up by slight
corrosion of copper piping or of brass equipment that is otherwise durable
may damage an entire batch of soap. Copper salts accelerate rancidity of

soaps and shorten the time that they can be stored before use. Traces of
metals may similarly alter the color of dyes. Lead equipment, otherwise
durable, is not permitted in the preparation of foods and beverages because
of the toxic properties imparted by very small quantities of lead salts. The
U.S. Bureau of Food and Drugs, for example, permits not more than 1 ppb
of lead in bottled drinking water [3].
Similarly, soft waters that pass through lead piping are not safe for drink-
ing purposes. The poisonous effects of small amounts of lead have been
known for a long time. In a letter to Benjamin Vaughn dated July 31, 1786,
Benjamin Franklin [4] warned against possible ill effects of drinking rain
water collected from lead roofs or consuming alcoholic beverages exposed
to lead. The symptoms were called in his time “dry bellyache” and were
accompanied by paralysis of the limbs. The disease originated because
New England rum distillers used lead coil condensers. On recognizing the
cause, the Massachusetts Legislature passed an act outlawing use of lead
for this purpose.
Another form of contamination is spoilage of food in corroded metal
containers. A cannery of fruits and vegetables once lost more than $1
million in one year before the metallurgical factors causing localized cor-
rosion were analyzed and remedied. Another company, using metal caps
on glass food jars, lost $0.5 million in one year because the caps perforated
by a pitting type of corrosion, thereby allowing bacterial contamination
of the contents.
5. Overdesign. Overdesign is common in the design of reaction vessels,
boilers, condenser tubes, oil-well sucker rods, pipelines transporting oil
and gas at high pressure, water tanks, and marine structures. Equipment
is often designed many times heavier than normal operating pressures or
applied stresses would require in order to ensure reasonable life. With
adequate knowledge of corrosion, more reliable estimates of equipment
life can be made, and design can be simplified in terms of materials and
labor. For example, oil-well sucker rods are normally overdesigned to
increase service life before failure occurs by corrosion fatigue. If the cor-
rosion factor were eliminated, losses would be cut at least in half. There
would be further savings because less power would be required to operate
a lightweight rod, and the expense of recovering a lightweight rod after
breakage would be lower.
Indirect losses are a substantial part of the economic tax imposed by corro-
sion, although it is difficult to arrive at a reasonable estimate of total losses.
In the event of loss of health or life through explosion, unpredictable failure of
chemical equipment, or wreckage of airplanes, trains, or automobiles through
sudden failure by corrosion of critical parts, the indirect losses are still more dif-
ficult to assess and are beyond interpretation in terms of dollars.
RISK MANAGEMENT 5
1.3 RISK MANAGEMENT
In general, risk, R, is defined as the probability, P, of an occurrence multiplied by

the consequence, C, of the occurrence; that is,
R = P ×C
Hence, the risk of a corrosion-related failure equals the probability that such a
failure will take place multiplied by the consequence of that failure. Consequence
is typically measured in financial terms—that is, the total cost of a corrosion
failure, including the cost of replacement, clean-up, repair, downtime, and so
on.
Any type of failure that occurs with high consequence must be one that
seldom occurs. On the other hand, failures with low consequence may be
tolerated more frequently. Figure 1.1 shows a simplified approach to risk
management.
Managing risk is an important part of many engineering undertakings today.
Managing corrosion is an essential aspect of managing risk. Firstly, risk manage-
ment must be included in the design stage, and then, after operation starts, main-
tenance must be carried out so that risk continues to be managed. Engineering
design must include corrosion control equipment, such as cathodic protection
systems and coatings. Maintenance must be carried out so that corrosion is moni-
tored and significant defects are repaired, so that risk is managed during the
operational lifetime.
4 Extreme Risk. Extensive risk

controls must be applied.
Consequence
3 High-Consequence Risk. Risk

controls required.
2
Moderate Risk. Some risk controls
1 required.
A B C D Low Risk. Risk controls may be

justified.
Probability
Figure 1.1. A simplified approach to risk management, indicating qualitatively the areas of
high risk, where both consequence and probability are high.
1.4 CAUSES OF CORROSION
The many causes of corrosion will be explored in detail in the subsequent chap-
ters of this book. In this introductory chapter, two parameters are mentioned: the
change in Gibbs free energy and the Pilling–Bedworth ratio [5].
1.4.1 Change in Gibbs Free Energy

The change in Gibbs free energy, ΔG, for any chemical reaction indicates the
tendency of that reaction to go. Reactions occur in the direction that lowers the
Gibbs free energy. The more negative the value of ΔG, the greater the tendency
for the reaction to go. The role of the change in Gibbs free energy is discussed
in detail in Chapter 3.
1.4.2 Pilling–Bedworth Ratio

Although many factors control the oxidation rate of a metal, the Pilling–
Bedworth ratio is a parameter that can be used to predict the extent to which
oxidation may occur. The Pilling–Bedworth ratio is Md/nmD, where M and D
are the molecular weight and density, respectively, of the corrosion product scale
that forms on the metal surface during oxidation; m and d are the atomic weight
and density, respectively, of the metal, and n is the number of metal atoms in a
molecular formula of scale; for example, for Al2O3, n = 2.
The Pilling–Bedworth ratio indicates whether the volume of the corrosion
product is greater or less than the volume of the metal from which the corrosion
product formed. If Md/nmD < 1, the volume of the corrosion product is less than
the volume of the metal from which the product formed. A film of such a corro-
sion product would be expected to contain cracks and pores and be relatively
nonprotective. On the other hand, if Md/nmD > 1, the volume of the corrosion
product scale is greater than the volume of the metal from which the scale
formed, so that the scale is in compression, protective of the underlying metal. A
Pilling–Bedworth ratio greater than 1 is not sufficient to predict corrosion resis-
tance. If Md/nmD >> 1, the scale that forms may buckle and detach from the
surface because of the higher stresses that develop. For aluminum, which forms
a protective oxide and corrodes very slowly in most environments, the Pilling–
Bedworth ratio is 1.3, whereas for magnesium, which tends to form a nonprotec-
tive oxide, the ratio is 0.8. Nevertheless, there are exceptions and limitations
to the predictions of the Pilling–Bedworth ratio, and these are discussed in
Chapter 11.
REFERENCES
1. Gerhardus H. Koch, Michiel P. H. Brongers, Neil G. Thompson, Y. Paul Virmani, and J. H.

Payer, Corrosion Costs and Preventive Strategies in the United States, Supplement to
PROBLEMS 7
Materials Performance, July 2002, Report No. FHWA-RD-01-156, Federal Highway

Administration, McLean, VA, 2002.
2. J. Kruger, Cost of metallic corrosion, in Uhlig’s Corrosion Handbook, 2nd edition, R. W.
Revie, editor, Wiley, New York, 2000, pp. 3–10.
3. http://www.fda.gov/fdac/features/1998/198_lead.html
4. Carl Van Doren, editor, Benjamin Franklin’s Autobiographical Writings, Viking Press,
New York, 1945, p. 671.
5. N. Pilling and R. Bedworth, J. Inst. Metals 29, 529 (1923).
GENERAL REFERENCES
R. Bhaskaran, N. Palaniswamy, N. S. Rengaswamy, and M. Jayachandran, Global cost of

corrosion—A historical review, in ASM Handbook, Vol. 13B, Corrosion: Materials,
ASM International, Materials Park, Ohio, 2005, pp. 621–628.
M. V. Biezma and J. R. San Cristóbal, Is the cost of corrosion really quantifiable? Corrosion
62 (12), 1051 (2006).
Geoff Davies, Materials for Automobile Bodies, Elsevier, Oxford, U.K., 2003.
Gerd Gigerenzer, Reckoning with Risk, Learning to Live with Uncertainty, Penguin Books,
London, 2003.
G. H. Koch, M. P. H. Brongers, N. G. Thompson, Y. P. Virmani, and J. H. Payer, Corrosion Cost
and Preventive Strategies in the United States, Report No. FHWA-RD-01-156, Federal
Highway Administration, U.S. Department of Transportation, McLean VA, March
2002.
G. H. Koch, M. P. H. Brongers, N. G. Thompson, Y. P. Virmani, and J. H. Payer, Direct costs
of corrosion in the United States, in ASM Handbook, Vol. 13A, Corrosion: Fundamen-
tals, Testing, and Protection, ASM International, Materials Park, OH, 2003, pp.
959–967.
W. Kent Muhlbauer, Pipeline Risk Management Manual: Ideas, Techniques, and Resources,
3rd edition, Elsevier, Oxford, U.K., 2004.
V. S. Sastri, E. Ghali, and M. Elboujdaini, Corrosion Prevention and Protection, Practical
Solutions, Wiley, Chichester, England, 2007.
E. D. Verink, Economics of corrosion, in Uhlig’s Corrosion Handbook, 2nd edition, R.
Winston Revie, editor, Wiley, New York, 2000, pp. 11–25.
PROBLEMS
1. A manufacturer provides a warranty against failure of a carbon steel product

within the first 30 days after sale. Out of 1000 sold, 10 were found to have
failed by corrosion during the warranty period. Total cost of replacement for
each failed product is approximately $100,000, including the cost of environ-
mental clean-up, loss of product, downtime, repair, and replacement.
(a) Calculate the risk of failure by corrosion, in dollars.

(b) If a corrosion-resistant alloy would prevent failure by corrosion, is an incremental
cost of $100 to manufacture the product using such an alloy justified? What would
be the maximum incremental cost that would be justified in using an alloy that
would prevent failures by corrosion?
2. Linings of tanks can fail because of salt contamination of the surface that
remains after the surface is prepared for the application of the lining. Between
15% and 80% of coating failures have been attributed to residual salt con-
tamination. The cost of reworking a failed lining of a specific tank has been
estimated at $174,000. [Reference: H. Peters, Monetizing the risk of coating
failure, Materials Performance 45(5), 30 (2006).]
(a) Calculate the risk due to this type of failure assuming that 20% of failures are
caused by residual salt contamination.
(b) If the cost of testing and removal of contaminating salts is $4100, is this additional
cost justified based on the risk calculation in (a)?
(c) Calculate the minimum percentage of failures caused by residual salt contamina-
tion at which the additional cost of $4100 for testing and removal of these salts is
justified.
2
ELECTROCHEMICAL
MECHANISMS
2.1 THE DRY-CELL ANALOGY AND FARADAY’S LAW
As described in Chapter 1, corrosion processes are most often electrochemical.

In aqueous media, the corrosion reactions are similar to those that occur in a
flashlight cell consisting of a center carbon electrode and a zinc cup electrode
separated by an electrolyte consisting essentially of NH4Cl solution* (Fig. 2.1).
An incandescent light bulb connected to both electrodes glows continuously, with
the electrical energy being supplied by chemical reactions at both electrodes. At
the carbon electrode (positive pole), chemical reduction occurs, and at the zinc
electrode (negative pole) oxidation occurs, with metallic zinc being converted
into hydrated zinc ions, Zn2+·nH2O.† The greater the flow of electricity through
the cell, the greater the amount of zinc that corrodes. The relationship is
*The function of carbon granules for conduction and manganese dioxide as depolarizer, both sur-
rounding the carbon electrode, need not concern us at this point.
†Ions in aqueous solution attach themselves to water molecules, but their number is not well-defined.
They differ in this way from gaseous ions, which are not hydrated. It is common practice, however,
to omit mention of the appended H2O molecules and to designate hydrated zinc ions, for example,
as Zn2+.

9
10 ELEC TROCHEMIC AL MECHANISMS
Figure 2.1. Dry cell.
quantitative, as Michael Faraday showed in the early nineteenth century. This is

the relationship now known as Faraday’s law:
Weight of metal reacting = kIt (2.1)
where I is the current in amperes (A), t is in seconds (s), and k is a constant called
the electrochemical equivalent. The value of k for zinc is 3.39 × 10−4 g/C (gram per
coulomb), the coulomb being defined as the amount of electricity represented
by 1 A flowing for 1 s. On short-circuiting the cell with a low-resistance metallic
connector, the zinc cup perforates by corrosion within a matter of hours; but
when the cell is left disconnected (open circuit), the zinc may remain intact for
years. The slow consumption of zinc occurring on open circuit is accounted for
largely by activity of minute impurities, like iron, embedded in the surface of zinc;
these impurities assume the same role as carbon and allow the flow of electricity
accompanied by corrosion of zinc. Current of this kind is called local-action
current, and the corresponding cells are called local-action cells. Local-action
current, of course, produces no useful energy, but acts only to heat up the
surroundings.
Any metal surface, similar to the situation for zinc, is a composite of elec-
trodes electrically short-circuited through the body of the metal itself (Fig. 2.2).
So long as the metal remains dry, local-action current and corrosion are not
observed. But on exposure of the metal to water or aqueous solutions, local-
action cells are able to function and are accompanied by chemical conversion
of the metal to corrosion products. Local-action current, in other words, may
DEFINITION OF ANODE AND C ATHODE 11
Figure 2.2. Metal surface enlarged, showing schematic arrangement of local-action cells.
account for the corrosion of metals exposed to water, salt solutions, acids, or
alkalies.
Whenever impurities in a metal constitute the electrodes of local-action cells,
their removal, as might be expected, appreciably improves corrosion resistance.
Accordingly, purified aluminum and magnesium are much more resistant to cor-
rosion in seawater or in acids than are the commercial varieties of these metals,
and high-purity zinc resists dilute hydrochloric acid much better than does com-
mercial zinc. However, it is not correct to assume, as was done many years ago
when the electrochemical theory was first proposed, that pure metals do not
corrode at all. As we will see later, local-action cells are also set up when there
are variations in the environment or in temperature. With iron or steel in aerated
water, for example, the negative electrodes are commonly portions of the iron
surface itself covered perhaps by porous rust (iron oxides); and positive elec-
trodes are areas exposed to oxygen, with the positive and negative electrode
areas interchanging and shifting from place to place as the corrosion reaction
proceeds. Accordingly, high-purity iron in air-saturated water corrodes at essen-
tially the same rate as impure or commercial iron. A difference in rates is observed
in acids, however, because impurities now enter predominantly as electrodes of
local-action cells. This matter is discussed in Section 7.3.
2.2 DEFINITION OF ANODE AND CATHODE
A combination of two electrical conductors (electrodes) immersed in an electro-

lyte is called a galvanic cell in honor of Luigi Galvani, a physician in Bologna,
Italy, who published his studies of electrochemical action in 1791. A galvanic cell
converts chemical energy into electrical energy. On short-circuiting such a cell
(attaching a low-resistance wire to connect the two electrodes), positive current
flows through the metallic path from positive electrode to negative electrode.
This direction of current flow follows an arbitrary convention, established before
anything was known about the nature of electricity, and is employed today
despite contemporary knowledge that only negative carriers, or electrons, move

in a metal. Electrons, of course, go from negative to positive pole, opposite to the
imaginary flow of positive carriers. Whenever current is said to flow, however,
without designating the sign of the carrier, positive current is always implied.
Within the electrolyte, current is carried by both negative and positive carriers,
known as ions (electrically charged atoms or groups of atoms). The current carried
by each ion depends on its mobility and electric charge. The total of positive and
negative current in the electrolyte of a cell is always exactly equivalent to the total
current carried in the metallic path by electrons alone. Ohm’s law—that is, I = E/R,
where I is the current in amperes, E the potential difference in volts, and R the
resistance in ohms—applies precisely, under conditions with which we are pres-
ently concerned, to current flow in electrolytes as well as in metals.
The electrode at which chemical reduction occurs (or + current enters the
electrode from the electrolyte) is called the cathode. Examples of cathodic reac-
tions are
1
H+ → H2 − e−
2
Cu 2 + → Cu − 2e −
Fe3+ → Fe2+ − e −
all of which represent reduction in the chemical sense.

The electrode at which chemical oxidation occurs (or + electricity leaves the
electrode and enters the electrolyte) is called the anode. Examples of anodic
reactions are
Zn → Zn 2 + + 2e −
Al → Al 3+ + 3e −
Fe2 + → Fe3+ + e −
These equations represent oxidation in the chemical sense. Corrosion of metals

usually occurs at the anode. Nevertheless, alkaline reaction products forming at
the cathode can sometimes cause secondary corrosion of amphoteric metals, such
as Al, Zn, Pb, and Sn, which corrode rapidly on exposure to either acids or
alkalies.
In galvanic cells, the cathode is the positive pole, whereas the anode is the
negative pole. However, when current is impressed on a cell from a generator or
an external battery—for example, as in electroplating—reduction occurs at the
electrode connected to the negative pole of the external current source, and this
electrode, consequently, is the cathode. Similarly, the electrode connected to the
positive pole of the generator is the anode. It is perhaps best, therefore, not to
T YPES OF CELLS 13
remember anode and cathode as negative and positive electrodes, or vice versa,
but instead to remember the cathode as the electrode at which current enters
from the electrolyte and remember the anode as the electrode at which current
leaves to return to the electrolyte. This situation is true whether current is
impressed on or drawn from the cell.
Cations are ions that migrate toward the cathode when electricity flows
through the cell (e.g., H+, Fe2+) and are always positively charged whether current
is drawn from or supplied to the cell. Similarly, anions are always negatively
charged (e.g., Cl−, OH−, SO2−4 ).
2.3 TYPES OF CELLS
There are three main types of cells that take part in corrosion reactions.
1. Dissimilar Electrode Cells. Examples of dissimilar electrode cells include:

the dry cell (discussed at the beginning of this chapter), a metal containing
electrically conducting impurities on the surface as a separate phase, a
copper pipe connected to an iron pipe, and a bronze propeller in contact
with the steel hull of a ship. Dissimilar electrode cells also include cold-
worked metal in contact with the same metal annealed, grain-boundary
metal in contact with grains, and a single metal crystal of definite orienta-
tion in contact with another crystal of different orientation.*
2. Concentration Cells. These are cells with two identical electrodes, each in
contact with a solution of different composition. There are two kinds of
concentration cells. The first is called a salt concentration cell. For example,
if one copper electrode is exposed to a concentrated copper sulfate solu-
tion, and another to a dilute copper sulfate solution (Fig. 2.3), on short-
circuiting the electrodes, copper dissolves (i.e., Cu → Cu2+ + 2e−) from the
electrode in contact with the dilute solution (anode) and plates out (i.e.,
Cu2+ + 2e− → Cu) on the other electrode (cathode). These reactions tend
to bring the two solutions to the same concentration.
The second kind of concentration cell, which in practice is the more
important, is called a differential aeration cell. This may include two iron
electrodes in dilute sodium chloride solution, the electrolyte around one
electrode being thoroughly aerated (cathode), and the other deaerated
*The various crystal faces of a metal, although initially exhibiting different potentials (tendencies to
corrode), tend to achieve the same potential in time when exposed to an environment that reacts
with the metal [1]. The most corrodible planes of atoms react first, leaving behind the least corrodible
planes; hence, the latter eventually are the only faces exposed regardless of the original orientation.
The corrosion rates continue to differ, however, because of differing absolute surface areas of what
were previously differing crystal faces. The most corrosion resistant crystal face of any metal is not
always the same, but varies with environment. For example, in dilute nitric acid, the (100) face of iron
is the least reactive crystallographic plane [2].
Figure 2.3. Salt concentration cell.
Figure 2.4. Differential aeration cell.
(anode) by, for example, bubbling nitrogen through the solution. The dif-
ference in oxygen concentration produces a potential difference and
causes current to flow (Fig. 2.4). This type of cell accounts for the pro-
nounced damage at crevices, which is called crevice corrosion. Crevices
are common in many engineering designs—for example, at the interface
of two pipes that are coupled together and at threaded connections. The
oxygen concentration is lower within crevices, and the areas of lower
oxygen concentration (inside the crevice) are anodic with respect to areas
of higher oxygen concentration (outside crevices). Differential aeration
cells can also cause pitting damage under rust (Fig. 2.5) and at the water
line—that is, at the water–air interface (Fig. 2.6). The amount of oxygen
reaching the metal that is covered by rust or other insoluble reaction
products is less than the amount that contacts other portions where the
permeable coating is thinner or nonexistent.
Differential aeration cells can also lead to localized corrosion at pits
(crevice corrosion) in stainless steels, aluminum, nickel, and other passive
metals that are exposed to aqueous environments, such as seawater.
3. Differential Temperature Cells. Components of these cells are electrodes
of the same metal, each of which is at a different temperature, immersed
T YPES OF CORROSION DAMAGE 15
Figure 2.5. Differential aeration cell

formed by rust on iron.
Figure 2.6. Water-line corrosion, showing

differential aeration cell.
in an electrolyte of the same initial composition. Less is known about the

practical importance and fundamental theory of differential temperature
cells than about the cells previously described. These cells are found in
heat exchangers, boilers, immersion heaters, and similar equipment.
In copper sulfate solution, the copper electrode at the higher temperature
is the cathode, and the copper electrode at the lower temperature is the
anode [3]. On short-circuiting the cell, copper deposits on the hot elec-
trode and dissolves from the cold electrode. Lead acts similarly, but for
silver the polarity is reversed.
For iron immersed in dilute aerated sodium chloride solutions, the hot
electrode is anodic to colder metal of the same composition; but after
several hours, depending on aeration, stirring rate, and whether the two
metals are short-circuited, the polarity may reverse [4, 5].
In engineering practice, cells responsible for corrosion may be a combination of

these three types.
2.4 TYPES OF CORROSION DAMAGE
Corrosion is often thought of only in terms of rusting and tarnishing. However,

corrosion damage occurs in other ways as well, resulting, for example, in failure
by cracking or in loss of strength or ductility. In general, most types of corrosion,
with some exceptions, occur by electrochemical mechanisms, but corrosion prod-
ucts are not necessarily observable and metal weight loss need not be appreciable
to result in major damage. The five main types of corrosion classified with respect
to outward appearance or altered physical properties are as follows:
1. General Corrosion, or Uniform Attack. This type of corrosion includes the

commonly recognized rusting of iron or tarnishing of silver. “Fogging” of nickel
and high-temperature oxidation of metals are also examples of this type.
Rates of uniform attack are reported in various units, with accepted termi-
nologies being millimeters penetration per year (mm/y) and grams per square
meter per day (gmd). Other units that are frequently used include inches penetra-
tion per year (ipy), mils (1 mil = 0.001 inch) per year (mpy), and milligrams per
square decimeter per day (mdd). These units refer to metal penetration or to
weight loss of metal, excluding any adherent or nonadherent corrosion products
on the surface. Steel, for example, corrodes at a relatively uniform rate in sea-
water of about 0.13 mm/y, 2.5 gmd, 25 mdd, or 0.005 ipy. These represent time-
averaged values. Generally, for uniform attack, the initial corrosion rate is greater
than subsequent rates [6]. Duration of exposure should always be given when
corrosion rates are reported because it is often not reliable to extrapolate a
reported rate to times of exposure far exceeding the test period.
Conversion of mm/y to gmd or vice versa requires knowledge of the metal
density. A given weight loss per unit area for a light metal (e.g., aluminum) rep-
resents a greater actual loss of metal thickness than the same weight loss for a
heavy metal (e.g., lead). Conversion tables are given in the Appendix, Section
29.8.
For handling chemical media whenever attack is uniform, metals are classi-
fied into three groups according to their corrosion rates and intended application.
These classifications are as follows:
A. <0.15 mm/y (<0.005 ipy)—Metals in this category have good corrosion

resistance to the extent that they are suitable for critical parts, for example,
valve seats, pump shafts and impellors, springs.
B. 0.15 to 1.5 mm/y (0.005 to 0.05 ipy)—Metals in this group are satisfactory
if a higher rate of corrosion can be tolerated, for example, for tanks,
piping, valve bodies, and bolt heads.
C. >1.5 mm/y (>0.05 ipy)—Usually not satisfactory.
2. Pitting. This is a localized type of attack, with the rate of corrosion being
greater at some areas than at others. If appreciable attack is confined to a rela-
tively small, fixed area of metal, acting as anode, the resultant pits are described
as deep. If the area of attack is relatively larger and not so deep, the pits are
called shallow. Depth of pitting is sometimes expressed by the pitting factor, the
ratio of deepest metal penetration to average metal penetration as determined
by the weight loss of the specimen. A pitting factor of unity represents uniform
attack (Fig. 2.7).
Iron buried in the soil corrodes with formation of shallow pits, whereas stain-
less steels immersed in seawater characteristically corrode with formation of
deep pits. Many metals, when subjected to high-velocity liquids, undergo a pitting
T YPES OF CORROSION DAMAGE 17
Figure 2.7. Sketch of deepest pit in

relation to average metal penetration
and the pitting factor.
type of corrosion called impingement attack, or sometimes corrosion-erosion.

Copper and brass condenser tubes, for example, are subject to this type of
attack.
Fretting corrosion, which results from slight relative motion (as in vibration)
of two substances in contact, one or both being metals, usually leads to a series
of pits at the metal interface. Metal-oxide debris usually fills the pits so that only
after the corrosion products are removed do the pits become visible.
Cavitation–erosion is the loss of material caused by exposure to cavitation,
which is the formation and collapse of vapor bubbles at a dynamic metal–liquid
interface—for example, in rotors of pumps or on trailing faces of propellers. This
type of corrosion causes a sequence of pits, sometimes appearing as a honeycomb
of small relatively deep fissures (see Uhlig’s Corrosion Handbook, 2nd edition,
R. W. Revie, editor, Wiley, New York, 2000, Fig. 12, p. 261).
3. Dealloying, Dezincification, and Parting. Dealloying is the selective

removal of an element from an alloy by corrosion. One form of dealloying,
dezincification, is a type of attack occurring with zinc alloys (e.g., yellow brass)
in which zinc corrodes preferentially, leaving a porous residue of copper and
corrosion products (Fig. 20.4). The alloy so corroded often retains its original
shape, and may appear undamaged except for surface tarnish, but its tensile
strength and ductility are seriously reduced. Dezincified brass pipe may
retain sufficient strength to resist internal water pressures until an attempt is
made to uncouple the pipe, or a water hammer occurs, causing the pipe to split
open.
Parting is similar to dezincification in that one or more reactive components
of the alloy corrode preferentially, leaving a porous residue that may retain the
original shape of the alloy. Parting is usually restricted to such noble metal alloys
as gold–copper or gold–silver and is used in gold refining. For example, an alloy
of Au–Ag containing more than 65% gold resists concentrated nitric acid as well
as does gold itself. However, on addition of silver to form an alloy of approxi-
mately 25% Au–75% Ag, reaction with concentrated HNO3 forms silver nitrate
and a porous residue or powder of pure gold.
Copper-base alloys that contain aluminum are subject to a form of corrosion
resembling dezincification, with aluminum corroding preferentially.
4. Intergranular Corrosion. This is a localized type of attack at the grain

boundaries of a metal, resulting in loss of strength and ductility. Grain-boundary
material of limited area, acting as anode, is in contact with large areas of grain
acting as cathode. The attack is often rapid, penetrating deeply into the metal
and sometimes causing catastrophic failures. Improperly heat-treated 18-8 stain-
less steels or Duralumin-type alloys (4% Cu–Al) are among the alloys subject to
intergranular corrosion. At elevated temperatures, intergranular corrosion can
occur because, under some conditions, phases of low melting point form and
penetrate along grain boundaries; for example, when nickel-base alloys are
exposed to sulfur-bearing gaseous environments, nickel sulfide can form and
cause catastrophic failures [7]. This type of attack is usually called sulfidation.
5. Cracking. If a metal cracks when subjected to repeated or alternate tensile

stresses in a corrosive environment, it is said to fail by corrosion fatigue. In the
absence of a corrosive environment, the metal stressed similarly, but at values
below a critical stress, called the fatigue limit or endurance limit, will not fail by
fatigue even after a very large, or infinite, number of cycles. A true endurance
limit does not commonly exist in a corrosive environment: The metal fails after
a prescribed number of stress cycles no matter how low the stress. The types of
environment causing corrosion fatigue are many and are not specific.
If a metal, subject to a constant tensile stress and exposed simultaneously to
a specific corrosive environment, cracks immediately or after a given time, the
failure is called stress-corrosion cracking. Both stress-corrosion cracking and
cracking caused by absorption of hydrogen generated by a corrosion reaction
follow this definition. Distinguishing differences between the two types of crack-
ing are discussed in Section 8.4. The stress may be residual in the metal, as from
cold working or heat treatment, or it may be externally applied. The observed
cracks are intergranular or transgranular, depending on the metal and the damag-
ing environment. Failures of this kind differ basically from intergranular corro-
sion, which proceeds without regard to whether the metal is stressed.
Almost all structural metals (e.g., carbon- and low-alloy steels, brass, stainless
steels, Duralumin, magnesium alloys, titanium alloys, nickel alloys, and many
others) are subject to stress-corrosion cracking in some environments. Fortu-
nately, either the damaging environments are often restricted to a few chemical
species, or the necessary stresses are sufficiently high to limit failures of this kind
in engineering practice. As knowledge accumulates regarding the specific media
that cause cracking and regarding the limiting stresses necessary to avoid failure
within a given time period, it will be possible to design metal structures without
incidence of stress-corrosion cracking. Highly stressed metal structures must be
designed with adequate assurance that stress-corrosion cracking will not occur.
REFERENCES
1. W. Tragert and W. D. Robertson, J. Electrochem. Soc. 102, 86 (1955).

2. C. S. Barrett and T. B. Massalski, Structure of Metals: Crystallographic Methods, Principles
and Data, 3rd revised edition, Pergamon Press, Oxford, U.K., 1980, p. 210.
PROBLEMS 19
3. N. Berry, Corrosion 2, 261 (1946).

4. H. H. Uhlig and O. Noss, Corrosion 6, 140 (1950).
5. V. Simpson, Jr., S.B. thesis, Department of Chemical Engineering, M.I.T., Cambridge,
MA, 1950.
6. R. W. Revie and N. D. Greene, Corros. Sci. 9, 755 (1969).
7. Bopinder Phull, Evaluating intergranular corrosion, in ASM Handbook, Vol. 13A,
Corrosion: Fundamentals, Testing, and Protection, ASM International, Materials Park,
OH, 2003, p. 570.
GENERAL REFERENCES
P. Elliott, Gallery of corrosion damage, in ASM Handbook, Vol. 13B, Corrosion: Materials,
ASM International, Materials Park, OH, 2005, pp. 631–646.
E. D. Verink, Designing to prevent corrosion, in Uhlig’s Corrosion Handbook, 2nd edition,
Wiley, New York, 2000, pp. 97–109.
PROBLEMS
1. Derive the general relation between mm/y and gmd.
2. Magnesium corrodes in seawater at a rate of 1.45 gmd. What is the rate in

mm/y? If this corrosion rates applies to lead, what is the corresponding rate
in mm/y?
3. Laboratory corrosion tests on three alloys in an industrial waste solution show

the following results:
Material Density of Weight Loss Pitting Factor

Material (g/cm2) (gmd)
A 2.7 40 1
B 9.0 62 2
C 7.8 5.6 9.2
Calculate maximum penetration in millimeters for each material at the end of

one year.
3
THERMODYNAMICS:
CORROSION TENDENCY AND
ELECTRODE POTENTIALS
3.1 CHANGE OF GIBBS FREE ENERGY
The tendency for any chemical reaction to go, including the reaction of a metal
with its environment, is measured by the Gibbs free-energy change, ΔG. The more
negative the value of ΔG, the greater the tendency for the reaction to go. For
example, consider the following reaction at 25 °C:
1
Mg + H 2 O (l) + O2 (g) → Mg(OH)2 (s) ΔG = −596,600 J
2
The large negative value of ΔG° (reactants and products in standard states)
indicates a pronounced tendency for magnesium to react with water and oxygen.
On the other hand, we have
1
Cu + H 2 O (l) + O2 (g) → Cu(OH)2 (s) ΔG = −119,700 J
2
The reaction tendency is less. Or we can say that the corrosion tendency of copper
in aerated water is not as pronounced as that of magnesium.
Finally, we have
21
22 THERMODYNAMICS: CORROSION TENDENCY AND ELEC TRODE POTENTIALS
3 3
Au + H 2 O (l) + O2 (g) → Au(OH)3 (s) ΔG = +65,700 J
2 4
The free energy is positive, indicating that the reaction has no tendency to go at all;
and gold, correspondingly, does not corrode in aqueous media to form Au(OH)3.
It should be emphasized that the tendency to corrode is not a measure of
reaction rate. A large negative ΔG may or may not be accompanied by a high
corrosion rate, but, when ΔG is positive, it can be stated with certainty that the
reaction will not go at all under the particular conditions described. If ΔG is
negative, the reaction rate may be rapid or slow, depending on various factors
described in detail later in this book.
In view of the electrochemical mechanisms of corrosion, the tendency for a
metal to corrode can also be expressed in terms of the electromotive force (emf)
of the corrosion cells that are an integral part of the corrosion process. Since
electrical energy is expressed as the product of volts by coulombs (joules, J), the
relation between ΔG in joules and emf in volts, E, is defined by ΔG = −nFE, where
n is the number of electrons (or chemical equivalents) taking part in the reaction,
and F is the Faraday (96,500 C/eq). The term ΔG can be converted from calories
to joules by using the factor 1 cal = 4.184 absolute joules.
Accordingly, the greater the value of E for any cell, the greater the tendency
for the overall reaction of the cell to go. This applies to any of the types of cells
described earlier.
3.2 MEASURING THE EMF OF A CELL
The emf of a cell, as set up in the laboratory or in the field, can be measured using
a voltmeter of high impedance, >1012 Ω (ohms). Alternatively, using a potentiome-
ter, the emf of the cell can be opposed with a known emf until no current flows
through a galvanometer in series with the cell. At exact balance (i.e., when the emf
of the cell is exactly balanced by the known emf), no current flows through the cell,
and the reading of the known emf indicates the exact emf of the cell. In making
these measurements, it is essential that any current that flows in the circuit is suffi-
ciently small that the cell is not polarized—that is, that the emf of the cell is not
changed because of the current flow. For this reason, sensitive galvanometers of
high input impedance, at least 1012 Ω, must be used, so that, if the potentiometer
and cell are unbalanced to the extent of 1 V, a current of only 10−12 A flows. Such a
current is not sufficient to polarize (temporarily alter the emf of) the cell.
3.3 CALCULATING THE HALF-CELL POTENTIAL—THE

NERNST EQUATION
Based on thermodynamics [1], an equation can be derived to express the emf of

a cell in terms of the concentrations of reactants and reaction products. The
general reaction for a galvanic cell is
C ALCUL ATING THE HALF-CELL POTENTIAL—THE NERNST EQUATION 23
lL + mM + → qQ + rR +
meaning that l moles of substance L plus m moles of substance M, and so on,

react to form q moles of substance Q, r moles of substance R, and so on. The
corresponding change of Gibbs free energy, ΔG, for this reaction is given by the
difference in molal free energy of products and reactants, where GQ represents
the molal free energy of substance Q, and so on.
ΔG = (qGQ + rGR + ) − (lGL + mGM + ) (3.1)
A similar expression is obtained for each substance in the standard state or arbi-
trary reference state, where the symbol G° indicates standard molal free
energy:
ΔG = (qGQ + rGR + ) − (lGL + mGM

+ ) (3.2)
If aL is the corrected concentration or pressure of substance L, called its activity,

the difference of free energy for L in any given state and in the standard state is
related to aL by the expression
l (GL − GL) = lRT ln aL = RT ln aLl (3.3)
where R is the gas constant (8.314 J/deg-mole), and T is the absolute temperature
(degrees Celsius + 273.16). Subtracting (3.2) from (3.1) and equating to corre-
sponding activities, we have the expression
a ⋅ aR q r
ΔG − ΔG = RT ln Ql m (3.4)
aL ⋅ aM
When the reaction is at equilibrium, there is no tendency for it to go, ΔG = 0,

and
aQq ⋅ aRr
=K
aLl ⋅ aM
m

where K is the equilibrium constant for the reaction. Hence
ΔG = − RT ln K (3.5)
On the other hand, when all the activities of reactants and products are equal to
unity, the logarithm term becomes zero (ln 1 = 0), and ΔG = ΔG°.
Since ΔG = −nFE, it follows that ΔG° = −nFE°, where E° is the emf when all
reactants and products are in their standard states (activities equal to unity).
Corresponding to (3.4), we have
RT aQq ⋅ aRr
E = E − ln (3.6)
nF aLl ⋅ aM
m

This is the Nernst equation, which expresses the exact emf of a cell in terms of
activities of products and reactants of the cell. The activity, aL, of a dissolved
substance L is equal to its concentration in moles per thousand grams of water
(molality) multiplied by a correction factor, γ, called the activity coefficient. The
activity coefficient is a function of temperature and concentration and, except for
very dilute solutions, must be determined experimentally. If L is a gas, its activity
is equal to its fugacity, approximated at ordinary pressures by the pressure in
atmospheres. The activity of a pure solid is arbitrarily set equal to unity. Similarly,
for water, with concentration essentially constant throughout the reaction, the
activity is set equal to unity.
Since the emf of a cell is always the algebraic sum of two electrode potentials
or of two half-cell potentials, it is convenient to calculate each electrode potential
separately. For example, for the electrode reaction
Zn 2 + + 2e − → Zn (3.7)
we have
RT (Zn)
φZn = φZn − ln (3.8)
2F (Zn 2 + )
where (Zn2+) represents the activity of zinc ions (molality × activity coefficient);
(Zn) is the activity of metallic zinc, the latter being a pure solid and equal, there-
fore, to unity; and φZn is the standard potential of zinc (equilibrium potential of
zinc in contact with Zn2+ at unit activity).
Since it is more convenient to work with logarithms to the base 10, the value
of the coefficient RT/F is multiplied by the conversion factor 2.303. Then, from
the value of R = 8.314 J/deg-mole, T = 298.2 K, and F = 96,500 C/eq, the coefficient
2.303 RT/F at 25 °C becomes 0.0592 V. This coefficient appears frequently in
expressions representing potentials or emf.
Measured or calculated values of standard potentials φ° at 25 °C are listed in
several reference books [2–4]. Some values are listed in Section 3.8, Table 3.2,
and in the Appendix, Section 29.9. Values of activity coefficients for various elec-
trolytes are given in the Appendix, Section 29.1, Table 29.1, and definitions and
rules applying to the use of activity coefficients are outlined in Section 29.1.
3.4 THE HYDROGEN ELECTRODE AND

THE STANDARD HYDROGEN SCALE
Since absolute potentials of electrodes are not known, it is convenient to assume

arbitrarily that the standard potential for the reaction
CONVENTION OF SIGNS AND C ALCUL ATION OF EMF 25
Figure 3.1. Hydrogen electrode.
2 H + + 2e − → H 2 (3.9)
is equal to zero at all temperatures. Hence,
RT pH
φH2 = 0 − ln +2 2 (3.10)
2F (H )
where pH2 is the fugacity of hydrogen in atmospheres and (H+) is the activity of
hydrogen ions. All values of electrode potentials, therefore, are with reference to
the hydrogen electrode. By measuring the emf of a cell made up, for example, of
a zinc and hydrogen electrode in zinc salt solution of known activity of Zn2+ and
H+, the standard potential, φ°, for zinc can be calculated; the accepted value is
−0.763 V.
The hydrogen electrode potential is measured by immersing a piece of plati-
nized platinum in a solution saturated with hydrogen gas at 1 atm (Fig. 3.1), or,
more conveniently, by the glass electrode, for which the potential is also revers-
ible to (in equilibrium with) hydrogen ions. The potential of the electrode equals
zero if the hydrogen ion activity and the pressure of hydrogen gas in atmospheres
are both unity. This is the standard hydrogen potential. Hence, the half-cell poten-
tial for any electrode is equal to the emf of a cell with the standard hydrogen
electrode as the other electrode. The half-cell potential for any electrode expressed
on this basis is said to be on the normal hydrogen scale or on the standard hydro-
gen scale, sometimes expressed as φH or φ(s.h.e.).
3.5 CONVENTION OF SIGNS AND CALCULATION OF EMF
In accord with the foregoing discussion, the standard potential of zinc, which is
not separately measurable, refers to the emf of a cell with two electrodes—zinc
and the standard hydrogen electrode:
Pt; H 2 , H + , Zn 2 + ; Zn (3.11)
The corresponding reaction, somewhat simplified, is written arbitrarily subtract-

ing the left-hand reduction reaction from the right-hand reduction reaction, or
Zn 2 + + H 2 → Zn + 2H + standard emf = −0.763 V (3.12)
The free-energy change, ΔG°, equals 0.763 × 2F joules; the positive value indicates
that the reaction is not thermodynamically possible as written, for products and
reactants in their standard states. On the other hand, for the cell
Zn; Zn 2 + , H +, H 2 ; Pt Standard emf = 0.763 V (3.13)
the corresponding reaction is Zn + 2H+ → Zn2+ + H2, the standard emf is positive,
and ΔG° is negative, indicating that the reaction is thermodynamically possible.
Clearly, the standard reduction potential for zinc is opposite in sign to the
standard oxidation potential for zinc.
It was agreed at the 1953 meeting of the International Union of Pure and
Applied Chemistry that the reduction potential for any half-cell electrode reac-
tion would be called the potential. This designation of sign has the advantage of
conforming to the physicist’s concept of potential defined as the work necessary
to bring unit positive charge to the point at which the potential is given. It also
has the advantage of corresponding in sign to the polarity of a voltmeter or
potentiometer to which an electrode may be connected. Thus, zinc has a negative
reduction potential and is also the negative pole of a galvanic cell of which the
standard hydrogen electrode is the other electrode. It is said to be negative to
the hydrogen electrode.
In setting up the emf of a cell, the foregoing conventions of sign dictate the
direction regarding spontaneous flow of electricity. If, on short-circuiting a cell,
positive current through the electrolyte within the cell flows from left to right,
then the emf is positive, and, correspondingly, the left electrode is anode and the
right electrode is cathode. If current flows within the cell from right to left, the
emf is negative.
To calculate the emf of the cell shown in Fig. 3.2, Cu; Cu2+, Zn2+; Zn, we can
first write the reduction reaction of the left electrode, Cu, as if it were cathode
(whether it is or not is clarified later):
Figure 3.2. Copper–zinc cell.

CONVENTION OF SIGNS AND C ALCUL ATION OF EMF 27
Cu 2 + + 2e − → Cu φ = 0.337 V (3.14)
and
0.0592 1
φCu = 0.337 − log (3.15)
2 (Cu 2 + )
The reduction reaction for the right electrode is
Zn 2 + + 2e − → Zn φ = −0.763 V (3.16)
and
0.0592 1
φZn = −0.763 − log (3.17)
2 (Zn 2 + )
Reaction (3.14) is subtracted from (3.16), multiplying, if necessary, by a numerical

factor so that the total electrons are canceled out. This results in the tentative
reaction for the cell,
Cu + Zn 2 + → Cu 2 + + Zn (3.18)*
The emf is obtained by adding, algebraically, the corresponding half-cell poten-

tials, (3.15) and (3.17). Although reversing a reaction changes the sign of poten-
tial, multiplying by any factor has no effect on either emf or φ° values, since the
tendency for a reaction to go is independent of the amount of substance reacting
(in contrast to the total free-energy change, which does depend on amount of
substance reacting):
0.0592 (Cu 2 + )
emf = φZn − φCu = −1.100 − log (3.19)
2 (Zn 2 + )
If the activities of Cu2+ and Zn2+ are chosen to be the same, the emf E is −1.100 V.
Since the emf is negative, current flows spontaneously from right to left within
the cell. This fixes the true polarity of the cell, with the left electrode, Cu, as posi-
tive (cathode) and the right electrode, Zn, as negative (anode). From the relation
ΔG = −nFE, the free-energy change of (3.18) is positive, and the reaction is,
therefore, not spontaneous as written, but goes instead in the opposite direction.
In other words, when current is drawn from the cell, Cu2+ plates out on the copper
electrode, and the zinc electrode corrodes.
*Reaction (3.18) is a simplification of the actual reaction. A more exact approach would include cal-
culation of the liquid-junction potential between CuSO4 and ZnSO4 and elimination of single-ion
activities, for which values are not measurable.
Similarly, the emf, polarity, and spontaneous reaction can be determined for
any cell for which half-cell reactions and standard potentials are known.
3.6 MEASUREMENT OF pH
Hydrogen ion activity is commonly expressed, for convenience, in terms of pH,

defined as
pH = − log (H+ )
Hence, for the half-cell reaction 2H+ + 2e− → H2, with the pressure of hydrogen
equal to 1 atm, we have
φ H2 = −0.0592 pH
Since pure water contains equal concentrations of H+ and OH− in equilibrium with
undissociated water, H2O → H+ + OH−, it is possible to calculate the activity of
either the hydrogen ion or the hydroxyl ion from the ionization constant, the value
of which at 25 °C is 1.01 × 10−14. Therefore, the pH of pure water at 25 °C is
− log 1.01 × 10 −14 = 7.0
If (H+) exceeds (OH−), as in acids, the pH is less than 7. If the pH is greater than
7, the solution is alkaline. The pH of strong acids can be negative, and the pH of
strong alkalies can be greater than 14.
At temperatures above 25 °C, the ionization constant of H2O is greater than
at 25 °C; therefore, above 25 °C, the pH of pure water is less than 7 (Table 3.1).
3.7 THE OXYGEN ELECTRODE AND DIFFERENTIAL AERATION CELL
The oxygen electrode can be represented by platinized platinum immersed in an

electrolyte saturated with oxygen. This electrode is particularly important to cor-
TABLE 3.1. Ionization Constant KW and pH of Pure Water

at Various Temperatures
Temperature (°C) KW pH
0 0.115 × 10−14 7.47

10 0.293 7.27
25 1.008 7.00
40 2.916 6.77
60 9.614 6.51
THE OX YGEN ELEC TRODE AND DIFFERENTIAL AER ATION CELL 29
rosion studies because of its role in differential aeration cells in the mechanism
of crevice corrosion and pitting.
The equilibrium for such an electrode is expressed as
1 1
H 2 O + O2 + e − → OH − φ = 0.401 V (3.20)
2 4
and
(OH − )
φO2 = 0.401 − 0.0592 log (3.21)
pO1 24
This reaction, however, unlike the hydrogen electrode reaction, is not strictly
reversible under practical conditions of measurement, and hence the measured
potential may vary with time and is not reproducible. The observed potential
tends to be less noble than the calculated reversible value. Nevertheless, it is
useful to know the direction of expected potential change as, for example, when
oxygen pressure is altered. For illustration, consider two oxygen electrodes in an
aqueous environment: one in contact with O2 at 1 atm (left) and the other with
O2 at 0.2 atm (right). The potentials of the left- and right-hand electrodes, respec-
tively, are as follows:
1 1
H 2 O + O2 (1 atm) + e − → OH − (3.22)
2 4
(OH − )
φ1 = 0.401 − 0.0592 log (3.23)
11 4
1 1
H 2 O + O2 (0.2 atm) + e − → OH − (3.24)
2 4
(OH − )
φ 2 = 0.401 − 0.0592 log (3.25)
0.21 4
Subtracting, Eqs. (3.24)–(3.22),
1 1
O2 (0.2 atm) → O2 (1 atm) (3.26)
4 4
Subtacting, Eqs. (3.25)–(3.23),
11 4 0.0592
φ 2 − φ1 = −0.0592 log 14
= log 0.2 = −0.0103 V (3.27)
0.2 4
The negative value of emf indicates that ΔG for (3.26) is positive, and hence
the reaction is not spontaneous as written. Instead, positive electricity flows
spontaneously within the cell from right to left. Therefore, the left-hand electrode,
(3.22), is positive (cathode) and the right-hand electrode, (3.24), is negative
(anode). This expresses the fact formulated earlier that, in any differential aera-
tion cell, the electrode in contact with lower-pressure oxygen tends to be the
anode, and the electrode in contact with higher-pressure oxygen tends to be the
cathode.
When a similar cell is made of iron electrodes instead of platinum, an adher-
ent, electrically conducting oxide of iron forms at cathodic areas; when in contact
with aerated solution, this oxide acts as an oxygen electrode. But at anodic areas,
Fe2+ forms, and the electrode acts as an iron electrode (φ° = −0.440 V). The oper-
ating emf of such a cell is much larger than that of the cell made up of platinum
electrodes, with the value being given by
0.0592 pO1 22
E = −0.440 − 0.401 − log (3.28)
2 ( Fe2 + )(OH − )2
If the ferrous ion activity at the anode is assumed equal to 0.1, the pH of water
at the cathode equal to 7.0, and the partial pressure of oxygen at the cathode
equal to that of air (0.2 atm), the operating emf of the corresponding cell is 1.27 V.
This is an appreciable value for resultant flow of current and accompanying cor-
rosion at the anode. In practice, the emf is less than this because of the irreversible
nature of the oxygen electrode, especially as approximated by an iron oxide film
on iron, but the emf would, in general, be larger than the small value calculated
for two platinum electrodes.
3.8 THE EMF AND GALVANIC SERIES
The Emf Series is an orderly arrangement of the standard potentials for all
metals. The more negative values correspond to the more reactive metals (Table
3.2). Position in the Emf Series is determined by the equilibrium potential of a
metal in contact with its ions at a concentration equal to unit activity. Of two
metals composing a cell, the anode is the more active metal in the Emf Series,
provided that the ion activities in equilibrium are both unity. Since unit activity
corresponds in some cases to impossible concentrations of metal ions because of
restricted solubility of metal salts, the Emf Series has only limited use for predict-
ing which metal is anodic to another.
Tin, for example, is noble to iron according to the Emf Series. This is also the
normal galvanic relationship of tin to iron in tinplate exposed to aerated aqueous
media. But on the inside of tin-plated iron containers (“tin cans”) in contact with
food, certain constituents of foods combine chemically with Sn2+ ions to form
soluble tin complexes. Reactions of this kind greatly lower the activity of Sn2+
ions with which the tin is in equilibrium, causing the potential of tin to become
much more active, perhaps even more active than iron. The polarity of the iron–
tin couple under these conditions reverses sign. The ratio of Sn2+ to Fe2+ within
the can must be very small for the reversal of polarity to occur, as can be calcu-
lated from φ° values for iron and tin in accord with the following reaction:
THE EMF AND GALVANIC SERIES 31
TABLE 3.2. Electromotive Force (Emf) Series

Electrode Reaction Standard Potential, φ°,
in volts at 25 °C
Au3+ + 3e− = Au 1.50

Pt2+ + 2e− = Pt ∼1.2
Pd2+ + 2e− = Pd 0.987
Hg2+ + 2e− = Hg 0.854
Ag+ + e− = Ag 0.800
Hg 22+ + 2e − = 2 Hg 0.789
Cu+ + e− = Cu 0.521
Cu2+ + 2e− = Cu 0.342
2H+ + 2e− = H2 0.000
Pb2+ + 2e− = Pb −0.126
Sn2+ + 2e− = Sn −0.136
Mo3+ + 3e− = Mo ∼−0.2
Ni2+ + 2e− = Ni −0.250
Co2+ + 2e− = Co −0.277
Tl+ + e− = Tl −0.336
In3+ + 3e− = In −0.342
Cd2+ + 2e− = Cd −0.403
Fe2+ + 2e− = Fe −0.440
Ga3+ + 3e− = Ga −0.53
Cr3+ + 3e− = Cr −0.74
Zn2+ + 2e− = Zn −0.763
Cr2+ + 2e− = Cr −0.91
Nb3+ + 3e− = Nb ∼−1.1
Mn2+ + 2e− = Mn −1.18
Zr4+ + 4e− = Zr −1.53
Ti2+ + 2e− = Ti −1.63
Al3+ + 3e− = Al −1.66
Hf4+ + 4e− = Hf −1.70
U3+ + 3e− = U −1.80
Be2+ + 2e− = Be −1.85
Mg2+ + 2e− = Mg −2.37
Na+ + e− = Na −2.71
Ca2+ + 2e− = Ca −2.87
K+ + e− = K −2.93
Li+ + e− = Li −3.05
Fe2 + + Sn → Sn 2 + + Fe (3.29)
and
0.0592 (Sn 2 + )
E = 0.136 − 0.440 − log (3.30)
2 ( Fe2 + )
The cell reverses polarity when E = 0. Hence,
(Sn 2 + ) 2
log = −0.304 × = −10.27
(Fe2 + ) 0.0592
or, the ratio (Sn2+)/(Fe2+) must be less than 5 × 10−11 for tin to become active to
iron. This small ratio can occur only through formation of tin complexes resulting
from certain organic substances in foods. Complexing agents in general, such as
EDTA, cyanides, and strong alkalies, tend to increase the corrosion rates of many
metals by reducing the metal-ion activity, thereby shifting metal potentials mark-
edly in the active direction.
Another factor that alters the galvanic position of some metals is the ten-
dency, especially in oxidizing environments, to form specific surface films. These
films shift the measured potential in the noble direction. In this state, the metal
is said to be passive (see Chapter 6). Hence, chromium, although normally near
zinc in the EMF Series, behaves galvanically more like silver in many air-satu-
rated aqueous solutions because of a passive film that forms over its surface. The
metal acts like an oxygen electrode instead of like chromium; hence, when
coupled with iron, chromium becomes the cathode and current flow accelerates
the corrosion of iron. In the active state (e.g., in hydrochloric acid), the reverse
polarity occurs; that is, chromium becomes anodic to iron. Many metals, especially
the transition metals of the periodic table, commonly exhibit passivity in aerated
aqueous solutions.
Because of the limitations of the Emf Series for predicting galvanic relations,
and also because alloys are not included, the Galvanic Series has been developed.
The Galvanic Series is an arrangement of metals and alloys in accord with their
actual measured potentials in a given environment. The potentials that determine
the position of a metal in the Galvanic Series may include steady-state values in
addition to truly reversible values; hence, alloys and passive metals are included.
The Galvanic Series for metals in seawater is given in Fig. 3.3. Some metals
occupy two positions in the Galvanic Series, depending on whether they are
active or passive, whereas in the Emf Series only the active positions are possible,
since only in this state is true equilibrium attained. The passive state, on the con-
trary, represents a nonequilibrium state in which the metal, because of surface
films, is no longer in normal equilibrium with its ions. Although only one Emf
Series exists, there can be several Galvanic Series because of differing complexing
tendencies of various environments and differences in tendency to form surface
films. In general, therefore, a specific Galvanic Series exists for each environment,
and the relative positions of metals in such Series may vary from one environ-
ment to another.
The damage incurred by coupling two metals depends not only on how far
apart they are in the Galvanic Series (potential difference), but also on their rela-
tive areas and the extent to which they are polarized (see Chapter 5). The poten-
tial difference of the polarized electrodes and the conductivity of the corrosive
environment determine how much current flows between them.
LIQUID JUNCTION POTENTIALS 33
Figure 3.3. Galvanic series in seawater [5]. (Reprinted with permission of ASM International®.
All rights reserved. www.asminternational.org.)
3.9 LIQUID JUNCTION POTENTIALS
In addition to potential differences between two metals in an electrolyte, poten-

tial differences also arise whenever two solutions of different composition or
concentration come into contact. The potential difference is called the liquid
TABLE 3.3. Characteristic Liquid Junction Potentials of

Salt Solutions [6]
Electrolyte Concentration
0.1 N 0.01 N
(−)HCl 35.65 mV 33.87 mV

KCl 8.87 8.20
NH4Cl 6.92 6.89
NaCl 2.57 2.63
(+)LiCl 0.00 0.00
junction potential, and its sign and magnitude are determined by the relative
mobility of ions and their concentration differences across the liquid junction.
For example, in a junction formed between dilute and concentrated hydrochloric
acid, H+ ions move with greater velocity than Cl− ions; mobility at infinite dilution
is 36 × 10−4 and 7.9 × 10−4 cm/s, respectively. Hence, the dilute aqueous solution
acquires a positive charge with respect to the concentrated solution. For potas-
sium chloride, the mobilities of K+ and Cl− are similar; hence, liquid junction
potentials between dilute and concentrated KCl are small in comparison with
HCl junctions. If the HCl solutions discussed previously are saturated with KCl,
so that most of the current across the boundary is carried by K+ and Cl− ions, the
liquid junction potential is decreased greatly. Use of a saturated KCl solution
whenever liquid junctions are formed is one practical approach to minimizing
liquid junction potentials.
Calculations of liquid junction potentials can be made on the basis of certain
assumptions, but the derivation of such calculations is relatively complex even
for simple junctions. Potentials of junctions formed between salt solutions of the
same concentration having a common ion, such as the chloride ion, are additive.
Characteristic values are given in Table 3.3, assigning zero arbitrarily to LiCl. For
example, the potential of the junction HCl(0.1 N) : KCl(0.1 N) is equal to 35.65 −
8.87 = 26.78 mV with KCl solution positive and HCl solution negative. On the
other hand, for the junction LiCl(0.1 N) : NH4Cl(0.1 N), the value is 0.00 − 6.92 =
−6.92 mV; the NH4Cl solution is negative, and the LiCl solution is positive. Values
at 0.01 N and 0.1 N are nearly alike and, except perhaps for strongly acidic or
basic solutions, the values are small and are not of great concern for most corro-
sion measurements.
3.10 REFERENCE ELECTRODES
In the measurement of emf, the observed value represents a tendency for simul-
taneous reactions to occur at both electrodes of the cell. Interest is usually
focused on the reaction that occurs at one electrode only. The criterion of com-
REFERENCE ELECTRODES 35
plete cathodic protection based on potential measurements is an example. Mea-

surements of this kind are made by using an electrode, called a reference electrode,
that has a fixed value of potential regardless of the environment in which it is
used. Any change in emf is the result of a change in potential of the electrode
under study and not of the reference electrode. Reference electrodes use stable
reversible electrode systems, as discussed in the following paragraphs. Details on
procedures for preparing reference electrodes are available elsewhere [7].
3.10.1 Calomel Reference Electrode

The calomel reference electrode has long been a standard reference electrode
used in the laboratory. It consists of mercury in equilibrium with Hg 2+
2 , the activ-
ity of which is determined by the solubility of Hg2Cl2 (mercurous chloride, or
calomel). The half-cell reaction is
Hg 2 Cl 2 + 2e − → 2 Hg + 2Cl − φ = 0.268 V
One design of electrode is illustrated in Fig. 3.4. Pure mercury covers a platinum
wire sealed through the bottom of a glass tube. The mercury is covered with
powdered mercurous chloride, which is only slightly soluble in potassium chloride
solution, the latter filling the cell. The activity of Hg 2+
2 depends on the concentra-
tion of KCl since the solubility product (Hg 22 + )(Cl − )2 is a constant. Potentials on
the standard hydrogen scale for various KCl concentrations are listed in
Table 3.4.
The saturated KCl electrode is convenient to prepare, but the potential is
somewhat more sluggish in responding to temperature changes than are the
unsaturated KCl electrodes. The 0.1 N electrode has the lowest temperature
coefficient.
Figure 3.4. A type of calomel reference electrode. (B. Eggins,

Biosensors: an Introduction, p. 56. Copyright Wiley and Teubner,
1996.)
TABLE 3.4. Potentials of Calomel Reference Electrodes

KCl φ (V) Temperature Coefficient
Concentration (V/°C)
0.1 N 0.3338 −0.88 × 10−4

1.0 N 0.2801 −2.75 × 10−4
Saturated KCl 0.2416 −6.6 × 10−4
The values cited neglect the liquid-junction potential at the KCl boundary,
which in the case of strong acids, for example, increases the absolute value an
average of several millivolts.
3.10.2 Silver–Silver Chloride Reference Electrode

The silver–silver chloride reference electrode, can be prepared by electroplating
with silver a platinum wire sealed into a glass tube. The silver coating is then
converted partly into silver chloride by making it anode in dilute hydrochloric
acid. Alternatively, a silver wire can be chloridized as just described. More details
on electrode preparation are available elsewhere [7]. When the silver–silver
chloride electrode is immersed in a chloride solution, the following equilibrium
is established:
AgCl + e − → Ag + Cl − φ = 0.222 V
Like the calomel electrode, the potential is more active the higher the KCl con-
centration. In 0.1 N KCl, the value is 0.288 V, and the temperature coefficient is
−4.3 × 10−4 V/°C. Potentials for other concentrations of KCl can be obtained by
substituting the corresponding mean ion activity of Cl− into the Nernst equation.
A schematic of a silver–silver chloride reference electrode is shown in
Fig. 3.5.
3.10.3 Saturated Copper–Copper Sulfate Reference Electrode

The saturated copper–copper sulfate reference electrode consists of metallic
copper immersed in saturated copper sulfate, as shown in Fig. 3.6. It is used pri-
marily in field measurements where the electrode must be resistant to shock and
where its usual large size minimizes polarization errors. The accuracy of this
electrode is adequate for most corrosion investigations, even though it falls some-
what below the precision obtainable with the calomel or silver chloride elec-
trodes. The half-cell reaction is
Cu 2 + + 2e − → Cu φ = 0.342 V
For saturated copper sulfate, the potential is 0.316 V, and the temperature coeffi-
cient is 7 × 10−4 V/°C [8].
REFERENCES 37
Figure 3.5. Schematic of a silver–silver chloride reference electrode.

(B. Eggins, Biosensors: an Introduction, p. 57. Wiley and Teubner,
1996.)
Figure 3.6. Copper–saturated copper sulfate reference

electrode.
REFERENCES
1. See, for example, G. Lewis, M. Randall, K. Pitzer, and L. Brewer, Thermodynamics,

McGraw-Hill, New York, 1961.
2. W. M. Latimer, The Oxidation States of the Elements and Their Potentials in Aqueous
Solutions, 2nd edition, Prentice-Hall, Englewood Cliffs, NJ, 1952.
3. G. Milazzo and S. Caroli, Tables of Standard Electrode Potentials, Wiley, Chichester,
1978.
4. M. S. Antelman, The Encyclopedia of Chemical Electrode Potentials, Plenum Press, New
York, 1982.
5. H. P. Hack, Evaluating galvanic corrosion, in ASM Handbook, Vol. 13A, Corrosion:

Fundamentals, Testing, and Protection, ASM International, Materials Park, OH, 2003, p.
563; ASTM G82–98(2003), Standard Guide for Development and Use of a Galvanic
Series for Predicting Galvanic Corrosion Performance, ASTM International, West Con-
shohocken, Pennsylvania; E. D. Verink, Designing to prevent corrosion, in Uhlig’s Cor-
rosion Handbook, 2nd edition, Wiley, New York, 2000, p. 99.
6. D. A. MacInnes, The Principles of Electrochemistry, Reinhold, New York, 1939; Dover,
New York, 1961.
7. D. J. G. Ives and G. J. Janz, Reference Electrodes: Theory and Practice, Academic Press,
New York, 1961, pp. 198–213.
8. S. Ewing, The Copper–Copper Sulfate Half-Cell for Measuring Potentials in the Earth,
Committee Report, American Gas Association, 1939, p. 10.
GENERAL REFERENCES
B. R. Eggins, Chemical Sensors and Biosensors, Wiley, Chichester, U.K., 2002.

D. R. Gaskell, Introduction to the Thermodynamics of Materials, 3rd edition, Taylor &
Francis, Washington, D.C., 1995.
E. Protopopoff, Potential measurements with reference electodes, in ASM Handbook, Vol.
13A, Corrosion: Fundamentals, Testing, and Protection, ASM International, Materials
Park, OH 2003, pp. 13–16.
PROBLEMS
In these problems, temperature is 25 °C unless otherwise stated.

1. Calculate the value for 2.303 RT/F at 50 °C.
2. Calculate the exact half-cell potential for the Ag–AgCl electrode in 1 M

NaCl.
3. Calculate the exact half-cell potential of zinc in 0.01 M ZnCl2.
4. Calculate the half-cell potential of the hydrogen electrode in a solution of

pH = 7 and partial pressure of H2 = 0.5 atm at 40 °C.
5. The emf of a cell made up of zinc (anode) and hydrogen electrode (cathode)
immersed in 0.5 M ZnCl2 is +0.590 V. What is the pH of the solution?
6. Calculate the theoretical tendency of zinc to corrode (in volts) with evolution
of hydrogen when immersed in 0.01 M ZnCl2 acidified to pH = 2.
7. Calculate the theoretical tendency for nickel to corrode (in volts) in deaer-
ated water of pH = 7. Assume that the corrosion products are H2 and Ni(OH)2,
the solubility product of which is 1.6 × 10−16.
PROBLEMS 39
8. (a) What is the emf of a cell made up of a copper electrode and a hydrogen
electrode ( pH2 = 2 atm) in copper sulfate (activity Cu2+ = 1) of pH = 1?
(b) What is the polarity of the cell and which electrode is anode?
9. (a) Calculate whether copper will corrode in deaerated CuSO4, pH = 0, to

form Cu2+ (activity = 0.1) and H2 (1 atm). What is the corrosion tendency
in volts?
(b) Similarly, calculate whether copper will corrode in deaerated KCN
(activity CN− = 0.5) of pH = 10, assuming that Cu(CN)−2 is formed, the
activity of which is 10−4.
Cu(CN)−2 + e − → 2CN − + Cu φ = −0.446 V
10. (a) Calculate the emf of the following cell:
Pt; Fe3+ (activity = 0.1), Fe2 + (activity = 0.001), Ag + (activity = 0.001); Ag
(b) Write the spontaneous reaction for the cell. What is the polarity and
which electrode is anode?
11. (a) Calculate the emf of a concentration cell made up of copper electrodes in
0.1 M CuSO4 and 0.5 M CuSO4, neglecting the liquid-junction potential.
(b) Write the spontaneous reaction of the cell and indicate which electrode
is anode.
12. (a) Calculate the emf of the following cell at 40 °C:

O2 (1 atm), Pt; H 2 O; O2 (0.1 atm), Pt
(b) What is the polarity and which electrode is anode?
13. (a) Calculate the emf of a cell made up of a hydrogen electrode ( pH2 = 1atm )
and an oxygen electrode ( pO2 = 0.5 atm ) in 0.5 M NaOH.
(b) What is the polarity and which electrode is anode? (Assume that the
oxygen electrode is reversible.)
14. Calculate whether silver will corrode if immersed in 0.1M CuCl2 to form solid
AgCl. What is the corrosion tendency in volts?
15. Calculate whether silver will corrode with hydrogen evolution in deaerated
KCN solution, pH = 9, when CN− activity = 1.0 and Ag(CN)−2 activity is
0.001.
16. Zinc is immersed in a solution of CuCl2. What is the reaction and at what
activity ratio Zn2+/Cu2+ will the reaction stop?
17. Calculate the emf of a cell made up of iron and lead electrodes in a solution
of Fe2+ and Pb2+ of equal activity. Which electrode tends to corrode when the
cell is short-circuited?
18. Calculate the emf as in Problem 17 in an air-saturated alkaline solution of

pH = 10. Which electrode corrodes on short-circuiting the cell? (Assume that
HPbO−2 forms as corrosion product and that its activity is 0.1; also assume
that iron is passive and that its potential approximates the oxygen
electrode.)
HPbO−2 + H 2 O + 2e − → Pb + 3OH − φ = −0.54 V
19. Given Fe2+ + 2e− → Fe, φ° = −0.440 V, and Fe3+ + e− → Fe2+, φ° = 0.771 V, cal-
culate φ° for Fe3+ + 3e− → Fe.
20. Given O2 + 2H2O + 4e− → 4OH−, φ° = 0.401 V, calculate φ° for O2 + 4H+ + 4e−
→ 2H2O.
21. Calculate the pressure (fugacity) of hydrogen required to stop corrosion of

iron immersed in 0.1 M FeCl2, pH = 3.
22. Calculate the pressure of hydrogen, as in Problem 21, in deaerated water with
Fe(OH)2 as the corrosion product. [Solubility product Fe(OH)2 = 1.8 ×
10−15.]
23. Calculate the pressure of hydrogen required to stop corrosion of cadmium

at 25 °C in deaerated water, with Cd(OH)2 as the corrosion product. [Solubil-
ity product Cd(OH)2 = 2.0 × 10−14.]
24. A copper storage tank containing dilute H2SO4 at pH = 0.1 is blanketed with
hydrogen at 1 atm. Calculate the maximum Cu2+ contamination of the acid
in moles Cu2+ per liter. What is the corresponding contamination if the hydro-
gen partial pressure is reduced to 10−4 atm?
Answers to Problems
1. 0.0641 V.
2. 0.233 V.
3. −0.827 V.
4. −0.426 V.
5. 3.28.
6. 0.709 V.
7. −0.111 V.
8. −0.405 V; H2 electrode is negative and is the anode.
9. (a) No; −0.307 V.
(b) Yes; 0.056 V.
10. (a) 0.208 V.
(b) Ag is negative and is the anode.
11. (a) 0.0096 V.
(b) 0.1M CuSO4 electrode is anode.
PROBLEMS 41
12. (a) 0.0155 V.

(b) 0.1 atm O2 electrode is negative and is the anode.
13. 1.225 V; H2 electrode is negative and is the anode.
14. Yes; 0.019 V.
15. No; emf = −0.045 V.
16. 1.45 × 1037.
17. 0.314 V; Fe.
18. −0.84 V; Pb.
19. −0.036 V.
20. 1.23 V.
21. 1.26 × 1010 atm.
22. 42 atm.
23. 0.42 atm.
24. 2.6 × 10−12; 2.6 × 10−8 mole/liter.
4
THERMODYNAMICS:
POURBAIX DIAGRAMS
4.1 BASIS OF POURBAIX DIAGRAMS
M. Pourbaix devised a compact summary of thermodynamic data in the form of

potential–pH diagrams, which relate to the electrochemical and corrosion behav-
ior of any metal in water. These diagrams, known as Pourbaix diagrams, are now
available for most of the common metals [1]. They have the advantage of showing
at a glance specific conditions of potential and pH under which the metal either
does not react (immunity) or can react to form specific oxides or complex ions;
that is, Pourbaix diagrams indicate the potential–pH domain in which each species
is stable.
From a corrosion engineering perspective, the value of Pourbaix diagrams is
their usefulness in identifying potential–pH domains where corrosion does not
occur—that is, where the metal itself is the stable phase. By controlling potential
(e.g., by cathodic protection) and/or by adjusting the pH in specific domains
identified using Pourbaix diagrams, it may be possible to prevent corrosion from
taking place. For example, in the potential–pH domain labeled “Fe (immunity),”
iron is stable, and no corrosion is predicted.
In general, thermodynamics is an excellent starting point for many corrosion
studies, and potential–pH diagrams are essential tools. For this reason, Pourbaix

43
44 THERMODYNAMICS: POURBAIX DIAGR AMS
diagrams continue to be developed for interpreting corrosion studies in specific

systems of engineering importance [2].
As every good engineer knows, however, predictions must be tested experi-
mentally and validated before using them, and predictions arrived at using Pour-
baix diagrams are no exception to this general rule.
4.2 POURBAIX DIAGRAM FOR WATER
Each line of a Pourbaix diagram represents conditions of thermodynamic equi-

librium for some reaction. The Pourbaix diagram for water is presented in Fig.
4.1. Above line b, oxygen is evolved in accord with the reaction H2O → 21 O2 +
2H+ + 2e−. For this equilibrium, the relationship between potential and pH is, from
the Nernst equation,
RT 1
φ = φ − 2.303 log
(H+ )
2
2F
–2 0 2 4 6 8 10 12 14 16
2
E(V) liberation of oxygen
1.6 and acidification
1.2 b
Potential (volts, S.H.E.)
0.8
0.4 thermodynamically stable

region of water at 1 atm.
0 a
–0.4
–0.8
liberation of hydrogen and
–1.2 alkalization
–1.6
–2 0 2 4 6 8 10 12 14 16
Figure 4.1. Pourbaix diagram for water at 25°C, showing the oxygen line, b, above which
oxygen is evolved, and the hydrogen line, a, below which hydrogen is evolved, from the
surface of an immersed electrode. Between these two lines, water is stable. (M. Pourbaix,
Atlas of Electrochemical Equilibria in Aqueous Solutions, 2nd English edition, p. 100, copyright
NACE International 1974 and CEBELCOR.)
POURBAIX DIAGR AM FOR IRON 45
With φ° = 1.229 (Appendix, Section 29.9), T = 298.2 K, R = 8.314 J/deg-mole, and

F = 96,500 C/eq, we have
φ = 1.229 − 0.0592 pH
Above line b, defined by this equation, oxygen is evolved at the surface of an

immersed electrode. Below this line, water is stable.
Below line a, hydrogen is evolved in accord with the reaction 2H+ + 2e− →
H2. Using the Nernst equation for this equilibrium, the relationship between
potential and pH is
RT 1
φ = φ − 2.303 log = −0.0592 pH
(H + )
2
2F
With φ° = 0 (Section 3.8, Table 3.2), we obtain
φ = −0.0592 pH
Below line a, represented by this equation, hydrogen gas is evolved from the
surface of an immersed electrode.
Between lines a and b, water is stable.
4.3 POURBAIX DIAGRAM FOR IRON
The Pourbaix diagram for iron is presented in Fig. 4.2.

A horizontal line represents a reaction that does not involve pH; that is,
neither H+ nor OH− is involved, as in the reaction, Fe2+ + 2e− → Fe. For this equi-
librium, using the Nernst equation, we obtain
RT 1
φ = φ − 2.303 log
nF (Fe2 + )
φ = −0.440 + 0.0296 log (Fe2 + )
If (Fe2+) is taken as 10−6, then φ = −0.617 V, a horizontal line on the Pourbaix

diagram.
A vertical line involves H+ or OH−, but not electrons; for example, 2Fe3+ +
3H2O → Fe2O3 + 6H+. In Figure 4.2, the vertical line separating Fe3+ from Fe2O3
corresponds to this reaction. For this equilibrium, we have
(H + )6
K=
( Fe3+ )2
log K = 6 log (H+ ) − 2 log ( Fe3+ )
Figure 4.2. Pourbaix diagram for the iron–water system at 25°C, considering Fe, Fe3O4, and
Fe2O3 as the only solid substances.
log K = −6 pH − 2 log (Fe3+ )
Since ΔG° = −RT ln K and ΔG° = −8240 J/mole, we obtain
log K = 1.43
log (Fe3+ ) = −0.72 − 3 pH
Taking (Fe3+) = 10−6, we have pH = 1.76.

In the Pourbaix diagram for iron, Fig. 4.2, the vertical line at pH 1.76 repre-
sents the equilibrium reaction, 2Fe3+ + 3H2O → Fe2O3 + 6H+. To the right of this
line (i.e., at pH > 1.76), Fe2O3 is the stable phase; and this oxide, as a protective
film, would be expected to provide some protection against corrosion. To the left
of this line (i.e., at pH < 1.76), ferric ions in solution are stable, and corrosion is
expected to take place without any protection afforded by a surface oxide film.
A sloping line involves H+, OH−, and electrons. For example, the sloping line
separating Fe2+ from Fe2O3 represents the reaction Fe2O3 + 6H+ + 2e− → 2Fe2+ +
3H2O. For this reaction, we have
RT (Fe2 + )2
φ = φ − 2.303 log
nF (H + )6
POURBAIX DIAGR AM OF ALUMINUM 47
Since φ° = 0.728 V and n = 2, we get
φ = 0.728 − 0.0296 ( Fe2 + )

0.0592 0.0592
φ = 0.728 − log (Fe2 + )2 + log (H + )6
2 2
φ = 0.728 − 0.0592 log (Fe2 + ) − 0.1776 pH
Taking (Fe2+) = 10−6, we obtain
φ = 1.082 − 0.1776 pH
This line in Fig. 4.2 represents the equilibrium, Fe2O3 + 6H+ + 2e− → 2Fe2+ + 3H2O.
To the right of this line, Fe2O3 is a stable phase that is expected to form a surface
oxide film that protects the underlying metal from corrosion. To the left of this
line, Fe2+ is a stable species in solution.
The pH values in Pourbaix diagrams are those of solution in immediate
contact with the metal surface. This value in some instances (e.g., Fe in aerated
H2O) differs from that of the bulk solution.
Soluble hypoferrites (HFeO−2 ) can form in very alkaline solutions within a
restricted active potential range. Soluble ferrates ( FeO2− 4 ) can form in alkaline
solutions at very noble potentials, but the stable field is not well-defined.
When any reaction involves ions other than H+ or OH−, it is assumed, in
general, that the activity equals 10−6. Thus the horizontal line at −0.62 V means
that iron will not corrode below this value to form a solution of concentration
> 10−6 M Fe2+ in accord with Fe → Fe2+ + 2e−, φ = −0.44 + (0.059/2)log (10−6) =
−0.62 V. If a value other that 10−6 is used, the lines separating the phases are
shifted (as can be seen in Figs. 4.3 and 4.4).
The fields marked Fe2O3 and Fe3O4 are sometimes labeled “passivation” on
the assumption that iron reacts in these regions to form protective oxide films.
This is correct only insofar as passivity is accounted for by a diffusion-barrier
oxide layer (Definition 2, Section 6.1). Actually, the Flade potential, above which
passivity of iron is observed in media such as sulfuric or nitric acid, parallels line
a and b, intersecting 0.6 V at pH = 0. For this reason, the passive film (Definition
1, Section 6.1) may not be any of the equilibrium stoichiometric iron oxides, as
is further discussed in Chapter 6.
4.4 POURBAIX DIAGRAM OF ALUMINUM
The Pourbaix diagram of aluminum, presented in Fig. 4.3, indicates that hydrargil-
lite, Al2O3·3H2O, is the stable phase between about pH 4 and 9 [3]. Indeed, this
film is considered to be responsible for the successful use of aluminum in
many structural applications. This diagram also predicts the amphoteric nature
Figure 4.3. Pourbaix diagram for the aluminum–water system at 25°C [2]. (M. Pourbaix, Atlas
of Electrochemical Equilibria in Aqueous Solutions, 2nd English edition, p. 171, copyright
of aluminum, with corrosion under highly acidic and highly alkaline conditions
and protection by an oxide film between about pH 4 and 9. Behavior of aluminum
is discussed further in Chapter 21.
4.5 POURBAIX DIAGRAM OF MAGNESIUM
The Pourbaix diagram of magnesium (Fig. 4.4) contrasts with that of aluminum
in that Mg2+ is the stable species in solution over most of the potential–pH range
[4]. The potential–pH domain in which magnesium is stable is well below the
domain in which water is stable; therefore, magnesium reduces water, and
hydrogen evolution is the cathodic reaction. Between pH about 8.5 and 11.5, a
protective film of oxide or hydroxide may provide some protection. At pH
greater than about 11.5, a stable film of Mg(OH)2 protects magnesium from
corrosion. Because of the very active value of the equilibrium potential of
the reaction, Mg2+ + 2e− → Mg, magnesium cannot be prepared by electrolysis
of its aqueous solutions, which would evolve hydrogen without forming
magnesium.
LIMITATIONS OF POURBAIX DIAGR AMS 49
Figure 4.4. Pourbaix diagram for the magnesium–water system at 25°C [3]. (M. Pourbaix,
Atlas of Electrochemical Equilibria in Aqueous Solutions, 2nd English edition, p. 141, copyright
4.6 LIMITATIONS OF POURBAIX DIAGRAMS
Since Pourbaix diagrams are based on thermodynamic data, they convey no

information on rates of reaction—that is, whether any possible reaction proceeds
rapidly or slowly when the energy changes are favorable. The data indicate the
conditions for which diffusion-barrier films may form on an electrode surface,
but they provide no measure of how effective such barrier films may be in the
−
presence of specific anions, such as SO2− 4 or Cl . Similarly, they do not indicate
the detailed conditions under which nonstoichiometric metal compound films are
possible; some of these films are important in determining observed corrosion
rates (see Chapter 6). However, the diagrams do clearly outline the nature of the
stoichiometric compounds into which any less stable compounds may transform
whenever equilibrium is achieved. Conventional Pourbaix diagrams do not
include alloys; for example, the corrosion of iron–nickel alloys cannot be accu-
rately predicted by superimposing conventional Pourbaix diagrams for iron and
nickel [5]. With these limitations, the diagrams usefully describe the equilibrium
status of a metal either as immersed in acids or alkalies or when a given potential
is impressed on it.
REFERENCES
1. Marcel Pourbaix, Atlas of Electrochemical Equilibria in Aqueous Solutions, translated

from the French by James A. Franklin, 2nd English edition, National Association of
Corrosion Engineers, Houston, TX, and Centre Belge d’Etude de la Corrosion (CEBEL-
COR), Brussels, Belgium, 1974.
2. M. J. Muñoz-Portero, J. García-Antón, J. L. Guiñón, and V. Pérez-Herranz, Corrosion 63 (7),
625 (2007).
3. Ref. 1., p. 171.
4. Ibid., p. 141.
5. W. T. Thompson, M. H. Kaye, C. W. Bale, and A. D. Pelton, Pourbaix diagrams for multi-
element systems, in Uhlig’s Corrosion Handbook, 2nd edition, R. W. Revie, editor, Wiley,
New York, 2000, pp. 125–136.
GENERAL REFERENCES
Marcel Pourbaix, Atlas of Electrochemical Equilibria in Aqueous Solutions, translated from

the French by James A. Franklin, 2nd English edition, National Association of Corro-
sion Engineers, Houston, Texas, and Centre Belge d’Etude de la Corrosion (CEBEL-
COR), Brussels, Belgium, 1974.
W. T. Thompson, M. H. Kaye, C. W. Bale, and A. D. Pelton, Pourbaix diagrams for multiele-
ment systems, in Uhlig’s Corrosion Handbook, 2nd edition, R. W. Revie, editor, Wiley,
New York, 2000, pp. 125–136.
E. D. Verink, Jr., Simplified procedure for constructing Pourbaix diagrams, in Uhlig’s
Corrosion Handbook, 2nd edition, R. W. Revie, editor, Wiley, New York, 2000, pp.
111–124.
PROBLEMS
1. Referring to the Pourbaix diagram for iron (Fig. 4.2), list equilibrium reactions
corresponding to lines separating (a) Fe and Fe3O4, (b) Fe3O4 and Fe2O3, and
(c) Fe2+ and Fe2O3. Calculate slopes ∂φ/∂pH in each case and compare with
the diagram.
2. Using the Pourbaix diagram for iron (Fig. 4.2), determine the direction of each
of the following four reactions in solution of pH 7 containing 0.06 ppm iron
in each of the following potential ranges.
Potential ranges:
(a) φ < −0.7 V.
(b) −0.6 < φ < −0.4 V.
(c) −0.4 V < φ < −0.2 V.
(d) −0.2 V < φ < +0.8 V.
(e) +0.80 V < φ
PROBLEMS 51
Reactions:
Fe2 + + 2e − → Fe
2 H + + 2e − → H 2
Fe2 O3 + 6 H + + 2e − → Fe2 + + 3H 2 O
O2 + 4 H + + 4e − → 2 H 2 O
Answers to Problem
1. (a) Fe3O4 + 8H+ + 8e− → 3Fe + 4H2O
∂φ/∂pH = −0.059
(b) ∂φ/∂pH = −0.18
5
KINETICS: POLARIZATION AND
CORROSION RATES
5.1 POLARIZATION
Thermodynamics—the equilibrium between metals and their environments—has

been discussed in the previous chapters. The concept of corrosion tendency is
based on thermodynamics. In practice, however, we are concerned primarily with
rates of corrosion—that is, with kinetics. Some metals with pronounced tendency
to react (e.g., aluminum) nevertheless react so slowly that they meet the require-
ments of a structural metal and may actually be more resistant in some media
than other metals that have inherently less tendency to react.
It must not be concluded, however, that considerations of equilibria are
irrelevant to the study of corrosion. Instead, a fundamental approach to nonequi-
librium states, along with calculation of corrosion rates, begins with the primary
consideration that equilibrium has been disturbed. In general, therefore, we must
know the equilibrium state of the system before we can appreciate the various
factors that control the rate at which the system tends toward equilibrium, that
is, the rate of corrosion.
An electrode is not at equilibrium when a net current flows to or from its
surface. The measured potential of such an electrode is altered to an extent that
depends on the magnitude of the external current and its direction. The direction

53
54 KINETICS: POL ARIZATION AND CORROSION R ATES
of potential change always opposes the shift from equilibrium and, hence, opposes
the flow of current, whether the current is impressed externally or is of galvanic
origin. When current flows in a galvanic cell, for example, the anode is always
more cathodic in potential and the cathode always becomes more anodic, with
the difference of potential between the anode and cathode becoming smaller as
current is increased. The potential change caused by net current to or from an
electrode, measured in volts, is called polarization.
Electrode kinetics is the study of reaction rates at the interface between an
electrode and a liquid. The science of electrode kinetics has made possible many
advances in the understanding of corrosion and the practical measurement of
corrosion rates. The interpretation of corrosion processes by superimposing elec-
trochemical partial processes was developed by Wagner and Traud [1]. Important
concepts of electrode kinetics that will be introduced in this chapter are the cor-
rosion potential (also called the mixed potential and the rest potential), corrosion
current density, exchange current density, and Tafel slope. The treatment of elec-
trode kinetics in this book is, of necessity, elementary and directed toward appli-
cation of corrosion science. For more detailed discussion of electrode kinetics,
the reader should refer to specialized texts listed at the end of the chapter.
5.2 THE POLARIZED CELL
Consider a cell made up of zinc in ZnSO4 solution and copper in CuSO4 solution
(the Daniell cell), the electrodes of which are connected to a variable resistance
R, voltmeter V, and ammeter A, as shown in Fig. 5.1. The potential difference
(emf) of zinc and copper electrodes of the cell without current flow is about 1 V.
If a small current is allowed to flow through the external resistance, the measured
potential difference falls below 1 V because both electrodes polarize. The voltage
continues to fall as the current increases. On complete short-circuiting (very small
external resistance), maximum current flows and the potential difference of
copper and zinc electrodes becomes almost zero.
Figure 5.1. Polarized copper–zinc cell.

THE POL ARIZED CELL 55
Figure 5.2. Polarization diagram for

copper–zinc cell.
The effect of net current flow on voltage of the Daniell cell can be repre-
sented by plotting a polarization diagram—that is, a graph showing potential, φ,
of copper and zinc electrodes (as described in Section 5.3, “How Polarization Is
Measured”) with total current, I, as shown in Fig. 5.2. The thermodynamic poten-
tials (no current flow through the cell) are given by φZn and φCu.
In Fig. 5.2, the zinc electrode polarizes along curve abc, and the copper
electrode polarizes along curve def. At a value of current through the ammeter
equal to I1, the polarization of zinc in volts is given by the difference between
the actual potential of zinc at b and the thermodynamic value a or φZn. Similarly,
the polarization of copper is given by the difference of potential e – d. The
potential difference of the polarized electrodes, b – e, is equal to the current i1
multiplied by the total resistance of both the external metallic resistance Rm
and the internal electrolytic resistance, Re, in series, or I1(Re + Rm). On short-
circuiting, the current becomes maximum, Imax. Then Rm can be neglected, and
the potential difference of both electrodes decreases to a minimum equal to
ImaxRe. The maximum current is equivalent to (65.38/2)Imax/F grams zinc corrod-
ing per second, where Imax is in amperes, F is equal to 96,500 C/eq, and 65.38/2
is the equivalent weight of zinc.
The cathodic reaction corresponds to the identical chemical equivalents of
copper depositing per second on the cathode. The corrosion rate of zinc can
exceed the indicated equivalent corrosion rate, Imax, only if a method is introduced
for reducing the polarization of zinc or copper, or both, thereby reducing the
slopes of abc or def, causing an approach to intersection at a larger value of I.
Similarly, any factor tending to increase polarization will decrease current through
the cell and decrease the corresponding corrosion rate of zinc. Obviously, the
polarization curves can never actually intersect, although they can approach each
other very closely if anodes and cathodes are closely spaced in media of moderate
to good conductivity. There will always be a finite potential difference accompa-

nying an observed flow of current.
Electrolytic cells that account for the corrosion of metals are analogous to
the short-circuited cell. The measured potential of a corroding metal, the mixed
potential of both polarized anodes and cathodes, is also referred to as the corro-
sion potential, φcorr. The value, Imax, is known as the corrosion current, Icorr. By
Faraday’s law, the corrosion rate of anodic areas on a metal surface is propor-
tional to Icorr, and hence the corrosion rate per unit area can always be expressed
as a current density. For zinc, a corrosion rate of 1 gmd is equivalent to 0.0342 A/
m2. For Fe corroding to Fe2+, the corresponding value is 0.0400 A/m2. Values for
other metals are listed in the Appendix (Section 29.8.2).
Referring to Fig. 5.2, we can calculate the corrosion rate of a metal if data
are available for the corrosion potential and for the polarization behavior and
thermodynamic potential of either anode or cathode. In general, the relative
anode–cathode area ratio for the corroding metal must also be known, since
polarization data are usually obtained under conditions where the electrode
surface is all anode or all cathode.
5.3 HOW POLARIZATION IS MEASURED
Referring to Fig. 5.3(a), showing a two-compartment cell separated by a sintered

glass disk, G, assume electrode B to be polarized by current from electrode D.
In order to achieve uniform current density at B, a three-compartment cell can
be used, with B in the center and two auxiliary electrodes in the outer compart-
ments. The probe L, sometimes called the Luggin capillary or salt bridge, of refer-
ence cell R (or of a salt bridge between R and B) is placed close to the surface
of B, thereby minimizing extraneous potentials caused by IR drop through the
electrolyte. The emf of cell B–R is recorded for each value of current as read on
ammeter A, allowing sufficient time for steady-state conditions. Polarization of
B, whether anode or cathode, is recorded in volts with reference to half-cell
electrode R for various values of current density. The potentials are often con-
verted to the standard hydrogen scale.
Figure 5.3(b) shows the type of cell that is commonly used in corrosion
studies to measure polarization, in which the working electrode (the electrode
being studied), two (for uniformity of current flow) counter electrodes, gas inlet
and outlet, Luggin capillary, and thermometer are all included [2].
The Luggin capillary can disturb the distribution of the current applied to
electrode (B) in Fig. 5.3(a). In addition, particularly in low conductivity solutions,
the distance of the tip of the Luggin capillary from the electrode being studied
[the distance between L and B in Fig. 5.3(a)] can have a significant effect on IR
drop that arises because of the current flow through the electrolyte.
Potentials can be measured with probe L adjusted at various distances from
B, with subsequent extrapolation to zero distance. This correction, as shown in
HOW POL ARIZATION IS MEASURED 57
(a)
(b)
Figure 5.3. (a) Cell for measuring polarization. (b) Schematic diagram of commonly used
polarization cell [2]. (Copyright ASTM INTERNATIONAL. Reprinted with permission.)
the next paragraph, is needed only when the measurements require highest accu-
racy, when the current densities are unusually high, or when the conductivity of
the electrolyte is unusually low, as in distilled water. This correction, however,
does not include any high-resistance reaction product film on the surface of the
electrode.
5.3.1 Calculation of IR Drop in an Electrolyte

The resistance of an electrolyte solution measuring l cm long and S cm2 in cross
section is equal to l/κS ohms, where κ is the specific conductivity. Hence, the IR
drop in volts equals il/κ, where i is the current density. For seawater, κ = 0.05 Ω−1 cm−1;
therefore, a current density of 1 × 10−5 A/cm2 (0.1 A/m2)(the magnitude of current
density that might be applied for cathodically protecting steel) produces an IR
drop correction for a 1-cm separation of probe from cathode equal to (1 ×
10−5 V)/0.05 = 0.2 mV. This value is negligible in establishing the critical minimum
current density for adequate cathodic protection. In some soft waters, however,
where κ may be 10−5 Ω−1 cm−1, the corresponding IR drop equals 1 V/cm.
5.4 CAUSES OF POLARIZATION
There are three types of electrode polarization: concentration polarization, acti-

vation polarization, and IR drop.
1. Concentration Polarization (Diffusion Overpotential). If copper is made

cathode in a solution of dilute CuSO4 in which the activity of cupric ion is rep-
resented by (Cu+2), then the potential φ1, in absence of external current, is given
by the Nernst equation
0.0592
φ1 = 0.337 + log (Cu 2 + ) (5.1)
2
When current flows, copper is deposited on the electrode, thereby decreasing

surface concentration of copper ions to an activity (Cu2+)s. The potential φ2 of the
electrode becomes
0.0592
φ 2 = 0.337 + log (Cu 2 + )s (5.2)
2
Since (Cu2+)s is less than (Cu2+), the potential of the polarized cathode is less
noble, or more active, than in the absence of external current. The difference of
potential, φ2 − φ1, is the concentration polarization, equal to
0.0592 (Cu 2 + )
φ 2 − φ1 = − log (5.3)
2 (Cu 2 + )s
The larger the current, the smaller the surface concentration of copper ion, or
the smaller the value of (Cu2+)s, thus the larger the corresponding polarization.
Infinite concentration polarization is approached when (Cu2+)s approaches zero
at the electrode surface; the corresponding current density that results in this
limiting lower value of (Cu2+)s is called the limiting current density. In practice,
CAUSES OF POL ARIZATION 59
polarization can never reach infinity; instead, another electrode reaction estab-
lishes itself at a more active potential than corresponds to the first reaction. In
the case of copper deposition, for example, the potential moves to that for hydro-
gen evolution, 2H+ + 2e− → H2, and hydrogen gas is liberated while copper is
simultaneously plated out.
If iL is the limiting current density for a cathodic process and i is the applied
current density, it can be shown [3] that
RT i
φ 2 − φ1 = − ln (5.4)
nF iL − i
As i approaches iL, φ2 − φ1 approaches −∞, that is, minus infinity. This is shown by
the plot of φ2 − φ1 versus i in Fig. 5.4.
The limiting current density (A/cm2) can be evaluated from the
expression
DnF
iL = c × 10 −3 (5.5)
δt
where D is the diffusion coefficient for the ion being reduced, n and F have their
usual significance, δ is the thickness of the stagnant layer of electrolyte next to
the electrode surface (about 0.05 cm in an unstirred solution), t is the transference
number of all ions in solution except the ion being reduced (equal to unity if
Figure 5.4. Dependence of concentration polarization at a cathode on applied current

density.
many other ions are present), and c is the concentration of diffusing ion in moles/
liter. Since D for all ions at 25oC in dilute solution, except for H+ and OH−, aver-
ages about 1 × 10−5 cm2/s, the limiting current density is approximated by
iL = 0.02 nc (5.6)
For H+ and OH−, D equals 9.3 × 10−5 and 5.2 × 10−5 cm2/s, respectively (infinite
dilution), so that the corresponding values of iL are higher.
Should the copper electrode be polarized anodically, concentration of copper
ion at the surface is larger than that in the body of solution. The ratio (Cu2+)/
(Cu2+)s then becomes less than unity and φ2 − φ1 of (5.3) changes sign. In other
words, concentration polarization at an anode polarizes the electrode in the
cathodic or noble direction, opposite to the direction of potential change when
the electrode is polarized as cathode. For a copper anode, the limiting upper value
for concentration polarization corresponds to formation of saturated copper salts
at the electrode surface. This limiting value is not as large as for cathodic polar-
ization where the Cu2+ activity approaches zero.
2. Activation Polarization. Activation polarization is caused by a slow elec-

trode reaction. The reaction at the electrode requires an activation energy in
order to proceed. The most important example is that of hydrogen ion reduction
at a cathode, H+ + e− → 21 H2. For this reaction, the polarization is called hydrogen
overpotential.
Overpotential is defined as the polarization (potential change) of an equilib-
rium electrode that results from current flow across the electrode–solution inter-
face. Overpotential, η, is the difference between the measured potential and the
thermodynamic, or reversible, potential;* that is,
η = φmeansured − φ reversible
At a platinum cathode, for example, the following reactions are thought to occur
in sequence:
H+ + e − → Hads
where Hads represents hydrogen atoms adsorbed on the metal surface. This rela-
tively rapid reaction is followed by another reaction, namely, adsorbed hydrogen
atoms combining to form hydrogen molecules and bubbles of gaseous
hydrogen:
2 Hads → H 2
*Overvoltage, on the other hand, is defined as polarization (potential change) of a corroding electrode
caused by flow of an applied current; that is, overvoltage, ε, is the difference between the measured
potential and the corrosion (or mixed) potential; that is, ε = φmeasured − φcorr.
CAUSES OF POL ARIZATION 61
This reaction is relatively slow, and its rate determines the value of hydrogen
overpotential on platinum. The controlling slow step of H+ discharge is not always
the same, but varies with metal, current density, and environment.
Pronounced activation polarization also occurs with discharge of OH− at an
anode accompanied by oxygen evolution:
1
2OH − → O2 + H 2 O + 2e −
2
The polarization corresponding to this reaction is called oxygen overpotential.

Overpotential may also occur with Cl− or Br− discharge, but the values at a given
current density are much smaller than those for O2 or H2 evolution.
Activation polarization is also characteristic of metal-ion deposition or dis-
solution. The value may be small for nontransition metals, such as silver, copper,
and zinc, but it is larger for the transition metals, such as iron, cobalt, nickel, and
chromium (see Table 5.1). The anion associated with the metal ion influences
metal overpotential values more than in the case of hydrogen overpotential. The
controlling step in the reaction is not known precisely, but, in some cases, it is
probably a slow rate of hydration of the metal ion as it leaves the metal lattice,
or dehydration of the hydrated ion as it enters the lattice.
Activation polarization, η, increases with current density, i, in accord with the
Tafel equation*:
i
η = β log
i0
where β and i0 are constants for a given metal and environment and are both
dependent on temperature. The exchange current density, i0, represents the current
density equivalent to the equal forward and reverse reactions at the electrode at
equilibrium. The larger the value of i0 and the smaller the value of β, the smaller
the corresponding overpotential.
A typical plot of activation polarization or overpotential for H+ discharge is
shown in Fig. 5.5. At the equilibrium potential for the hydrogen electrode
(−0.059pH), for example, overpotential is zero. At applied current density, i1, it is
given by η, the difference between measured and equilibrium potentials. Although
usually listed as positive, hydrogen overpotential values are negative and, corre-
spondingly, oxygen overpotential values are positive on the φ scale.
3. IR Drop. Polarization measurements include a so-called ohmic potential

drop through a portion of the electrolyte surrounding the electrode, through a
metal-reaction product film on the surface, or both. An ohmic potential drop
always occurs between the working electrode and the capillary tip of the refer-
ence electrode. This contribution to polarization is equal to iR, where I is the
*Named after J. Tafel [Z. Phys. Chem. 50, 641 (1904)], who first proposed a similar equation to express
hydrogen overpotential as a function of current density.
TABLE 5.1. Overpotential Values

i
η = β log
i0
Temperature β i0 η at 1 mA/cm2
Metal (°C) Solution (volts) (A/m2) (V)a
Hydrogen Overpotential
Pt (smooth) 20 1 N HCl 0.03 10 0.00
25 0.1 N NaOH 0.11 0.68 0.13
Pd 20 0.6 N HCl 0.03 2 0.02
Mo 20 1 N HCl 0.04 10−2 0.12
Au 20 1 N HCl 0.05 10−2 0.15
Ta 20 1 N HCl 0.08 10−1 0.16
W 20 5 N HCl 0.11 10−1 0.22
Ag 20 0.1 N HCl 0.09 5 × 10−3 0.30
Ni 20 0.1 N HCl 0.10 8 × 10−3 0.31
20 0.12 N NaOH 0.10 4 × 10−3 0.34
Bi 20 1 N HCl 0.10 10−3 0.40
Nb 20 1 N HCl 0.10 10−3 0.40
Fe 16 1 N HCl 0.15 10−2 0.45
25 4% NaCl pH 1–4 0.10 10−3 0.40 (Stern)
Cu 20 0.1 N HCl 0.12 2 × 10−3 0.44
20 0.15 N NaOH 0.12 1 × 10−2 0.36
Sb 20 2 N H2SO4 0.10 10−5 0.60
Al 20 2 N H2SO4 0.10 10−6 0.70
Be 20 1 N HCl 0.12 10−5 0.72
Sn 20 1 N HCl 0.15 10−4 0.75
Cd 16 1 N HCl 0.20 10−3 0.80
Zn 20 1 N H2SO4 0.12 1.6 × 10−7 0.94
Hg 20 0.1 N HCl 0.12 7 × 10−9 1.10
20 0.1 N H2SO4 0.12 2 × 10−9 1.16
20 0.1 N NaOH 0.10 3 × 10−11 1.15
Pb 20 0.01–8 N HCl 0.12 2 × 10−9 1.16
Oxygen Overpotential
Pt (smooth) 20 0.1 N H2SO4 0.10 9 × 10−8 0.81
20 0.1 N NaOH 0.05 4 × 10−9 0.47
Au 20 0.1 N NaOH 0.05 5 × 10−9 0.47
Metal Overpotential (Deposition)

Zn 25 1 M ZnSO4 0.12 0.2 0.20(Bockris)
Cu 25 1 M CuSO4 0.12 0.2 0.20(Bockris)
Fe 25 1 M FeSO4 0.12 10−4 0.60(Bockris)
Ni 25 1 M NiSO4 0.12 2 × 10−5 0.68(Bockris)
a
1 mA/cm2 = 10 A/m2.
Source: Data from B. E. Conway, Electrochemical Data, Elsevier, New York, 1952; Modern Aspects
of Electrochemistry, J. Bockris, editor, Academic Press, New York, 1954; M. Stern, J. Electrochem. Soc.
102, 609 (1955); H. Kita, J. Electrochem. Soc. 113, 1095 (1966).
HYDROGEN OVERPOTENTIAL 63
Figure 5.5. Hydrogen overvoltage as a function of current density.
current density, and R, equal to l/κ, represents the value in ohms of the resistance
path of length l cm and specific conductivity κ. The product, iR, decays simultane-
ously with shutting off the current, whereas concentration polarization and acti-
vation polarization usually decay at measurable rates. The iR contribution can be
calculated as described in Section 5.3.1.
Note: Concentration polarization decreases with stirring, whereas activation

polarization and iR drop are not affected significantly.
5.5 HYDROGEN OVERPOTENTIAL
The polarization term that controls the corrosion rate of many metals in deaer-
ated water and in nonoxidizing acids is hydrogen overpotential. In accord with
the previously discussed definition of polarization, hydrogen overpotential is the
difference of potential between a cathode at which hydrogen is being evolved,
φmeasured, and a hydrogen electrode at equilibrium in the same solution; that is,
H 2 overpotential = φmeasured − (−0.059pH)
Hydrogen overpotential, therefore, is measured in the same way as polarization

is measured. Ideally, hydrogen overpotential includes only the activation polar-
ization term corresponding to the reaction 2H+ + 2e− → H2, but reported values
often include iR drop and sometimes concentration polarization as well.
The absolute values of hydrogen overpotential for a given metal decrease

with:
1. Increasing temperature (i0 increases). For metals that corrode by hydro-

gen evolution, decreasing hydrogen overpotential is one factor accounting
for increase of corrosion as the temperature is raised.
2. Roughening of the surface. A sandblasted surface has a lower hydrogen
overpotential than a polished surface. Greater area and improved catalytic
activity of a rough surface account for the observed effect.
3. Decreasing current density. The Tafel equation,
i
η = β log
i0
is obeyed within the region of applied current density, i, below the limiting
current density for concentration polarization, and above the exchange
current density, i0. The term β is equal to 2.3RT/αF, where α is a constant
and the other terms have their usual significance. The term α is approxi-
mately 2 for platinum and palladium and is approximately 0.4–0.6 for Fe,
Ni, Cu, Hg, and several other metals. Although hydrogen overpotential
values usually differ in acid compared with alkaline media, values are not
greatly sensitive to pH within either range.
Stern [4] showed that for a corroding metal we have
i + ir + icorr
η = β log
i0
where ir is the reverse current for the reaction H2 → 2H+ + 2e−, which varies with
potential and which, at equilibrium, is equal to i0. This equation describes the
small observed slope of dη/d log i for small values of impressed current density,
i, with the slope increasing as i approaches icorr + ir and reaching the true Tafel
slope, β, at i >> ir + icorr. Similarly, the overpotential for a noncorroding metal can
be represented by a modified Tafel equation,
i + ir
η = β log
i0
This equation holds from zero to finite values of i (Fig. 5.5). Values of ir deter-
mined from measured values of η also follow the Tafel equation, but with a slope
of opposite sign.
The slow step in the discharge of hydrogen ions on platinum, or palladium,
as described earlier, appears to be recombination of adsorbed hydrogen atoms.
This assumption is consistent, from kinetic considerations, with an observed value
HYDROGEN OVERPOTENTIAL 65
of α = 2. For iron, the value of α is approximately 0.5 and, correspondingly, β =

0.1. To account for these values, the proposal has been made that the slow step
in the hydrogen evolution reaction on iron is probably
H+ + Hads → H 2 − e −
The same slow step may apply to various metals having intermediate values of
hydrogen overpotential (e.g., iron, nickel, copper).
For metals of high hydrogen overpotential, such as mercury and lead, the
slow discharge of the hydrated hydrogen ion is apparently the slow step:
H + → Hads − e −
For many metals at high current densities, this slow discharge step is also
the controlling reaction. The slow discharge step may, instead, be the reduction
of H2O,
1
H 2 O → OH − + H 2 − e −
2
The reduction of water as the controlling reaction applies generally to metals in

alkaline solutions at high and low current densities.
The rapidity with which Hads combines to form H2, either by combination
with itself or with H+, is affected by the catalytic properties of the electrode
surface. A good catalyst, such as platinum or iron, leads to a low value of hydro-
gen overpotential, whereas a poor catalyst, such as mercury or lead, accounts for
a high value of overpotential. If a catalyst poison, like hydrogen sulfide or certain
arsenic or phosphorus compounds, is added to the electrolyte, it retards the rate
of formation of molecular H2 and increases the accumulation of adsorbed hydro-
gen atoms on the electrode surface.* The increased concentration of surface
hydrogen favors entrance of hydrogen atoms into the metal lattice, causing
hydrogen embrittlement (loss of ductility), and, in some stressed high-strength
ferrous alloys, may induce spontaneous cracking, called hydrogen cracking (see
Section 8.4). Catalyst poisons increase absorption of hydrogen whether the metal
*Increase of hydrogen overpotential normally decreases the corrosion rate of steel in acids, but pres-
ence of sulfur or phosphorus in steels is observed instead to increase the rate. This increase probably
results from the low hydrogen overpotential of ferrous sulfide or phosphide, either existing in the
steel as separate phases or formed as a surface compound by reaction of iron with H2S or phosphorus
compounds in solution. It is also possible [4] that the latter compounds, in addition, stimulate the
anodic dissolution reaction, Fe → Fe2+ + 2e− (reduce activation polarization), or alter the anode–
cathode area ratio.
Similarly, arsenious oxide in small amount accelerates corrosion of steel in acids (e.g., H2SO4),
perhaps forming arsenides, but when present in larger amount (e.g., 0.05% As2O3 in 72% H2SO4), it
is an effective corrosion inhibitor, probably because elementary arsenic, having a high hydrogen
overpotential, deposits out at cathodic areas. Tin salts have the same inhibiting effect and have been
used to protect steels from attack by pickling acids during descaling operations.
is polarized by externally applied current or by a corrosion reaction with accom-

panying hydrogen evolution. For this reason, some oil-well brines containing H2S
are difficult to handle in low-alloy steel tubing subject to the usual high stresses
of a structure extending several thousand feet underground. Slight general cor-
rosion of the tubing produces hydrogen, a portion of which enters the stressed
steel to cause hydrogen cracking. In the absence of hydrogen sulfide, general
corrosion occurs, but without hydrogen cracking. High-strength steels, because of
their limited ductility, are more susceptible to hydrogen cracking than are low-
strength steels, but hydrogen enters the lattice in either case, tending to blister
low-strength steels instead.
Values of β, i0, and of η at 1 mA/cm2 for H+ discharge are given in Table 5.1.
As can be seen from the table, values of hydrogen overpotential vary greatly with
the metal. Values also change with concentration of electrolyte, but the effect,
comparatively, is not large.
5.6 POLARIZATION DIAGRAMS OF CORRODING METALS
Polarization diagrams of corroding metals, sometimes called Evans diagrams, are

graphs of potential versus log current or log current density. They were originally
developed by U. R. Evans at the University of Cambridge in England, who rec-
ognized the usefulness of such diagrams for predicting corrosion behavior [5]. To
establish a polarization diagram, the usual electrodes that are employed, in addi-
tion to the electrode being studied (the “working” electrode), are the reference
electrode and the inert counter (or auxiliary) electrode that is usually made of
platinum. The design of a 1-liter electrochemical cell used in many corrosion
laboratories [2] is shown in Fig. 5.3(b). A gas bubbler in used for atmospheric
control—for example, to deaerate the solution or to saturate the solution with a
specific gas.
The measurements are usually made using a potentiostat—an instrument
that automatically maintains the desired potential between the working and ref-
erence electrodes by passing the appropriate current between the working and
counter electrodes. Various electronic circuits for potentiostat design have been
presented in the corrosion literature and their applications to corrosion studies
have been discussed [6].
Alternatively, depending on the type of measurements to be made, a galva-
nostatic circuit, consisting of a power supply, resistor, ammeter, and potentiome-
ter, can be used. The current between working and counter electrodes is controlled,
and the potential of the working electrode with respect to the reference electrode
is measured.
In experimentally establishing a polarization diagram, the first measurement
is usually that of the corrosion potential, φcorr, when the applied current, Iappl, is
zero. The working electrode is then polarized either anodically or cathodically to
establish one of the dashed lines in Fig. 5.6. The polarization procedure is then
repeated, but with Iappl reversed, to obtain the second dashed line. Using the
POL ARIZATION DIAGR AMS OF CORRODING METALS 67
Figure 5.6. Polarization diagram.
potentiostat, polarization may be carried out either in potential steps (i.e., poten-
tiostatically) or continuously (i.e., potentiodynamically). Having established φ
versus log Iappl on the more noble and the more active sides of the corrosion
potential, the complete polarization diagram is then constructed, as shown in Fig.
5.6 for metal M. In this system, the oxidation reaction may be the dissolution of
metal, M → Mz+ + ze−, and the reduction reaction may be symbolized as Rn+ +
ne− → R. In an aerated neutral or basic aqueous solution, the reduction reaction
could be O2 + 2H2O + 4e− → 4OH−, whereas in a deaerated acid, the reduction
reaction could be 2H+ + 2e− → H2.
For any corroding metal, the chemical equivalents of metal going into solu-
tion at the anodic sites are equal to the chemical equivalents of reduction prod-
ucts produced at cathodic sites. In terms of corrosion current, for a given area of
metal surface, Ia = Ic; that is, the anodic and cathodic currents are equal in mag-
nitude. The corresponding current density, ia, at anodic areas depends on the
fraction of metal surface, Aa, that is anode, and, similarly, ic depends on Ac. In
general, Ia/Aa = ia and Ic/Ac = ic; but ia = ic only if Aa = Ac—that is, if 50% of the
surface is anodic and 50% is cathodic. Under the latter condition, the general
relation for any anode–cathode area ratio Iappl = Ia − Ic can be translated to cor-
responding current densities iappl = ia − ic.
When the electrode is polarized at sufficiently high current densities to shift
the potential more than approximately 100 mV from the corrosion potential, the
reverse, or “back” reactions, are usually negligible [7]; depending on the direction
of Iappl, the metal surface acts either as all anode or all cathode. Accordingly, for
anodic polarization, iappl ≈ ia, and, similarly, for cathodic polarization, iappl ≈ ic. Tafel
slopes can then be determined (see paragraph “Activation Polarization,” Section
5.4). By extrapolating from the anodic Tafel region to the reversible (equilibrium)
anode potential, φA, the exchange current density, i0a, for the reaction Mz+ + ze−
→ M is determined; that is, the equal rates of oxidation and reduction reactions
are expressed as a current density. Similarly, by extrapolating from the Tafel
region to the reversible potential φc, the exchange current density i0c for the
cathodic reaction is determined. By extrapolating from either the anodic or
cathodic Tafel region to the corrosion potential φcorr, where ic = ia, the corrosion
rate icorr can be determined for the condition that Aa = Ac (anode–cathode area
ratio = 1). Although the latter condition often closely approximates the true situ-
ation, a more exact approximation to the corrosion rate would require informa-
tion about the actual anode–cathode area ratio.
5.7 INFLUENCE OF POLARIZATION ON CORROSION RATE
Both resistance of the electrolyte and polarization of the electrodes limit the
magnitude of current produced by a galvanic cell. For local-action cells on the
surface of a metal, electrodes are in close proximity to each other; consequently,
resistance of the electrolyte is usually a secondary factor compared to the more
important factor of polarization. When polarization occurs mostly at the anodes,
the corrosion reaction is said to be anodically controlled (see Fig. 5.7). Under
anodic control, the corrosion potential is close to the thermodynamic potential
of the cathode. A practical example is impure lead immersed in sulfuric acid,
where a lead sulfate film covers the anodic areas and exposes cathodic impurities,
such as copper. Other examples are magnesium exposed to natural waters and
iron immersed in a chromate solution.
When polarization occurs mostly at the cathode, the corrosion rate is said to
be cathodically controlled. The corrosion potential is then near the thermody-
namic anode potential. Examples are zinc corroding in sulfuric acid and iron
exposed to natural waters.
Resistance control occurs when the electrolyte resistance is so high that the
resultant current is not sufficient to appreciably polarize anodes or cathodes. An
example occurs with a porous insulating coating covering a metal surface. The
corrosion current is then controlled by the IR drop through the electrolyte in
pores of the coating.
It is common for polarization to occur in some degree at both anodes and
cathodes. This situation is described as mixed control.
The extent of polarization depends not only on the nature of the metal and
electrolyte, but also on the actual exposed area of the electrode. If the anodic area
of a corroding metal is very small, caused, for example, by porous surface films,
there may be considerable anodic polarization accompanying corrosion, even
INFLUENCE OF POL ARIZATION ON CORROSION R ATE 69
Figure 5.7. Types of corrosion control.

corroding metal when anode area equals
one-half of cathode area.
though measurements show that unit area of the bare anode polarizes only slightly
at a given current density. Consequently, the anode–cathode area ratio is also an
important factor in determining the corrosion rate. If current density is plotted
instead of total corrosion current, as, for example, when the anode area is half the
cathode area, corresponding polarization curves are shown in Fig. 5.8.

zinc amalgam in deaerated HCl.
An important experiment that illustrates the electrochemical mechanism of

corrosion was performed by Wagner and Traud [1]. They measured the corrosion
rate of a dilute zinc amalgam in an acid calcium chloride mixture and the cathodic
polarization of mercury in the same electrolyte. The current density equivalent
to the corrosion rate was found to correspond to the current density necessary
to polarize mercury to the corrosion potentiual of the zinc amalgam (Fig. 5.9).
In other words, mercury atoms of the amalgam composing the majority of the
surface apparently act as cathodes, or hydrogen electrodes,* and zinc atoms act
as anodes of corrosion cells. The amalgam polarizes anodically very little, and the
corrosion reaction is controlled almost entirely by the rate of hydrogen evolution
at cathodic areas. Consequently, it is the high hydrogen overpotential of mercury
that limits the corrosion rate of amalgams in nonoxidizing acids. A piece of plati-
num coupled to the amalgam considerably increases the rate of corrosion because
hydrogen is more readily evolved from a low-overpotential cathode at the oper-
ating emf of the zinc–hydrogen electrode cell.
The very low corrosion rate and the absence of appreciable anodic polariza-
tion explain why amalgams in corresponding metal salt solutions exhibit corro-
sion potentials closely approaching the reversible potential of the alloyed
component. For example, the corrosion potential of cadmium amalgam in CdSO4
solution is closer to the thermodynamic value for Cd → Cd2+ + 2e− than is
observed for pure cadmium in the same solution. The steady-state corrosion rate
of pure cadmium is appreciably higher than that of cadmium amalgam, leading
*Mercury in aqueous solutions acts first as a mercury electrode, but, when cathodically polarized, all
mercury ions in solution are deposited before H+ is discharged. Any conducting surface on which H+
ions are discharged acts as a polarized hydrogen electrode and can be so considered in evaluating a
corrosion cell.
C ALCUL ATION OF CORROSION R ATES FROM POL ARIZATION DATA 71
to greater deviation of the measured corrosion potential from the corresponding

thermodynamic value. In general, the steady-state potential of any metal more
active than hydrogen (e.g., iron, nickel, zinc, cadmium) in an aqueous solution of
its ions deviates from the true thermodynamic value by an amount that depends
on the prevailing corrosion rate accompanied by H+ discharge. The measured
value tends to be more noble than the true value. This situation also holds for
the steady-state potentials of more noble metals (e.g., copper, mercury) which
undergo corrosion in the presence of dissolved oxygen.
5.8 CALCULATION OF CORROSION RATES FROM

POLARIZATION DATA
The corrosion current can be calculated from the corrosion potential and the
thermodynamic potential if the equation expressing polarization of the anode or
cathode is known, and if the anode–cathode area ratio can be estimated. For
corrosion of active metals in deaerated acids, for example, the surface of the metal
is probably covered largely with adsorbed H atoms and can be assumed, there-
fore, to be mostly cathode. The thermodynamic potential is −0.059 pH, and if icorr
is sufficiently larger than i0 for H+ → 21H2 − e−, the Tafel equation expresses
cathodic polarization behavior. Then,
(
φcorr = − 0.059 pH + β log
icorr
i0 ) (5.7)
from which icorr and the equivalent corrosion rate can be calculated. Stern [4]
showed that calculated corrosion rates for iron, using (5.7) and employing empiri-
cal values for β and i0, were in excellent agreement with observed rates. Typical
values are given in Table 5.2.
TABLE 5.2. Comparison of Calculated and Observed Corrosion Currents for Pure Iron in
Various Deaerated Acids [4]
Solution φHcorr + 0.059pH β i0 icorr (μA/cm2)
(volts, S.H.E.) (V) (μA/cm2)
Calculated Observed
0.1 M Citric acid −0.172 0.084 0.093 10.4 11.5

pH = 2.06
0.1 M Malic acid −0.158 0.083 0.015 1.2 1.2
pH = 2.24
4% NaCl + HCl
pH = 1 −0.203 0.100 0.10 10.5 11.1
pH = 2 −0.201 0.100 0.11 11.0 11.3
Subsequently, Stern and Geary [8] derived the very important and useful
equation, now known as the Stern–Geary equation,
Iappl ⎛ βcβa ⎞
I corr = (5.8)
2.3Δφ ⎝ βc + βa ⎠
or
1 ⎛ β cβ a ⎞
I corr =
2.3R ⎝ βc + βa ⎠
where βc and βa refer to Tafel constants for the cathodic and anodic reactions,
respectively, and Iappl/Δφ is the polarization slope (the reciprocal of the polariza-
tion resistance, R = Δφ/Iappl) in the region near the corrosion potential, for which
the change of potential, Δφ, with Iappl is essentially linear (for derivation, see the
Appendix, Section 29.2). Under conditions of slight polarization, for which Δφ is
not more than about 10 mV, the anode–cathode area ratio, which need not be
known, remains essentially constant and conditions otherwise at the surface of
the corroding metal are largely undisturbed.
If corrosion is controlled by concentration polarization at the cathode, as
when oxygen depolarization is controlling, Equation (5.8) simplifies to
βa Iappl
I corr = (5.9)
2.3 Δφ
Although values of β are relatively well known for H+ discharge, they are not as
generally available for other electrode reactions. Stern showed, however, that the
majority of reported β values are between 0.06 and 0.12 V. If βc is known to be
0.06 V, for example, and βa is between 0.06 and 0.12 V, the calculated corrosion
current is within at least 20% of the correct value. Under other assumptions, the
corrosion rate can be calculated to at least a factor of 2.
The general validity of Eqs. (5.8) and (5.9) is shown by data summarized in
Fig. 5.10. The observed corrosion current, corresponding to data on corrosion of
nickel in HCl and on corrosion of steels and cast iron in acids and in natural
waters, extends over six orders of magnitude. Some exchange current densities
for Fe3+ → Fe2+ − e− on passive surfaces are included because the same principle
applies in calculating i0 for a noncorroding electrode as in calculating Icorr for a
corroding electrode. Also, straight lines are shown representing values calculated
on the basis of several assumed β values within which most of the empirical data
lie. Equations (5.7), (5.8), and (5.9) have been widely used with considerable
success for determining the corrosion rates of various metals in aqueous environ-
ments at ambient and elevated temperatures.
The linear polarization method has obvious advantages in calculating instan-
taneous corrosion rates for many metals in a wide variety of environments and
under various conditions of velocity and temperature. It can also be used to
ANODE– C ATHODE AREA R ATIO 73
Figure 5.10. Relation between polarization slope at low applied current densities and
observed corrosion or exchange current densities [9]. (Copyright ASTM INTERNATIONAL.
Reprinted with permission.)
evaluate inhibitors and protective coatings, as well as for detecting changes of

corrosion rate with time. A correction is required if an IR drop is involved in the
measurement.
The Stern–Geary equation has been modified to minimize errors under par-
ticular conditions. Errors in Eq. (5.8) are especially significant in systems in which
the corrosion potential is close to one of the reversible potentials—that is, is
outside the Tafel region. Mansfeld and Oldham [10] have developed a set of
equations that provides less error than Eq. (5.8) when this situation applies (see
Appendix, Section 29.2).
5.9 ANODE–CATHODE AREA RATIO
The reduction of H+ at a platinum cathode at a given rate is accompanied by

the simultaneous reverse reaction at a lower rate for H2 oxidizing to H+. The
oxidation and reduction reactions are assumed to take place on the same surface
sites. At equilibrium, the forward and reverse reactions are equal and the equiva-
lent current density is called the exchange current density. For a corroding metal,
the anode and cathode reactions are distinct and different; one is not merely the
reverse reaction of the other. Hence, the oxidation reaction can take place only
on sites of the metal surface that are different from those on which reduction
takes place. For this situation, the distance between anode and cathode may vary
from atomic dimensions to a separation of many meters.
Correspondingly, an anode–cathode area ratio exists, and since the observed
polarization of anodic or cathodic sites depends, in part, on the area over which
oxidation or reduction occurs, the anode–cathode area ratio is an important
factor in the observed corrosion rate.
Stern [11] developed the general relation for which anodic and cathodic
polarization follows Tafel behavior and IR drop is negligible. Using a typical
polarization diagram, as illustrated in the Appendix, Section 29.2, Fig. 29.1, we
obtain
Ic
φ′c = φc − βc log (5.10)
Ac i0 c
and
Ia
φ′a = φa + βa log (5.11)
Aai0 a
where subscripts a and c refer to anode and cathode, respectively, φ′ is the polar-
ized potential, φ is the thermodynamic potential, β is the Tafel slope, I is
the current per unit metal surface area, Aa is the fraction of surface that is
anode such that Aa + Ac = 1, and i0a and i0c are the exchange current densities
for the anode and cathode reactions, respectively. At steady state,
φc′ = φa′ = φcorr and I a = I c = I corr . Then
βc log I corr = φc − φcorr + βc log Ac i0 c (5.12)
and
φcorr = φa + βa log I corr − βa log Aa i0 a (5.13)
Substituting (5.13) into (5.12), we obtain
φc − φa βa βc
log I corr = + log Aa i0 a + log Ac i0 c (5.14)
βc + βa βc + βa βc + βa
Since Aa = 1 − Ac, we get

ELEC TROCHEMIC AL IMPEDANCE SPEC TROSCOPY 75
d log I corr βa 1 βc 1
=− + (5.15)
dAc 2.3(βc + βa ) (1 − Ac) 2.3(βc + βa) Ac
βc(1 − Ac) − βa Ac
= (5.16)
2.3(βc + βa) Ac Aa
Maximum Icorr occurs at d log Icorr/dAc = 0—that is, when the numerator of (5.16)
equals zero. This occurs when Ac = βc/(βc + βa). If, as is frequently observed, βc =
βa, then the maximum corrosion rate occurs at Ac = 21—that is, at an anode–
cathode area ratio of unity. At any other anode–cathode area ratio, the corrosion
rate is less, reaching zero at a ratio equal to either zero or infinity.
5.10 ELECTROCHEMICAL IMPEDANCE SPECTROSCOPY
Electrochemical methods based on alternating currents can be used to obtain

insights into corrosion mechanisms and to establish the effectiveness of corrosion
control methods, such as inhibition and coatings. In an alternating-current circuit,
impedance determines the amplitude of current for a given voltage. Impedance
is the proportionality factor between voltage and current. In electrochemical
impedance spectroscopy (EIS), the response of an electrode to alternating poten-
tial signals of varying frequency is interpreted on the basis of circuit models of
the electrode/electrolyte interface. Figure 5.11 shows two circuit models that can
Cdl
Rs
Rp
(a)
Cdl
Rs
W
Rp
(b)
Figure 5.11. (a) Electrical equivalent circuit model used to represent an electrochemical
interface undergoing corrosion in the absence of diffusion control. Rp is the polarization
resistance, Cdl is the double layer capacitance, Rp is the polarization resistance, and Rs is the
solution resistance [15]. (b) Electrical equivalent circuit model when diffusion control applies;
W is the Warburg impedance [13].
be used for analyzing EIS spectra. The simplest model for characterizing the
metal–solution interface, Fig. 5.11(a), includes the three essential parameters, Rs
(the solution resistance), Cdl (the capacitance of the double layer), and Rp (the
polarization resistance). When direct-current measurements are carried out (i.e.,
frequency is zero), the impedance of the capacitor approaches infinity. In parallel
electrical circuits, the circuit with the smallest impedance dominates, with the
result that, under these conditions, the sum of Rs and Rp is measured. If Rs if sig-
nificant, the corrosion rate is underestimated.
When diffusion control is important, another element, ZD, sometimes called
the Warburg impedance, is added in series with Rp, as shown in Fig. 5.11(b).
In electrochemical impedance spectroscopy, the impedance of the corroding
metal is analyzed as a function of frequency. A sinusoidal potential change is
applied to the corroding electrode at a number of frequencies, ω. At each fre-
quency, the resulting sinusoidal current waveform is out of phase with the applied
potential signal by an amount, the phase angle, θ, that depends on the circuit
parameters. The current amplitude is inversely proportional to the impedance of
the interface. The electrochemical impedance, Z(ω), is the frequency-dependent
proportionality factor in the relationship between the voltage signal and the
current response,
E(ω)
Z (ω) = (5.17)
i(ω)
where E is the voltage signal, E = E0 sin(ωt); i is the current density, i = i0sin

(ωt + θ); Z is the impedance (ohm-cm2); and t is the time (seconds) [12].
Impedance is a complex number that is described by the frequency-
dependent modulus, |Z|, and the phase angle, θ, or, alternatively, by the real
component, Z′, and the imaginary component, Z″. The mathematical convention
for separating the real and imaginary components is to multiply the magnitude
of the imaginary component by j [ = −1] and report the real and imaginary
values as a complex number.
The equations for electrochemical impedance are [13]
E = Ereal + Eimaginary = E ′ + jE ′′ (5.18)

I = I real + I imaginary = I ′ + jI ′′ (5.19)
E ′ + jE ′′
Z = Z ′ + jZ ′′ = (5.20)
I ′ + jI ′′
Z ′′
tanθ = (5.21)
Z′
Z = (Z ′)2 + (Z ′′)2
2
(5.22)
In electrochemical impedance analysis, three different types of plots are com-

monly used: Nyquist plots (complex plane, showing −Z″ versus Z′) and two dif-
THEORY OF C ATHODIC PROTEC TION 77
Figure 5.12. Electrochemical impedance data for cast 99.9% magnesium in pH 9.2 sodium
borate presented in the Nyquist format [14]. (Reproduced by permission of ECS, The Electro-
chemical Society.)
ferent types of Bode plots, showing the impedance magnitude versus log frequency
and showing phase angle versus log frequency. One example of each type of plot
is shown in Figs. 5.12 and 5.13. Figure 5.12 illustrates electrochemical impedance
data for cast 99.9% magnesium in pH 9.2 sodium borate in the Nyquist format.
This figure shows a single capacitive semicircle, indicating that the only process
occurring is charge transfer.
Figure 5.13 shows Bode magnitude and phase angle plots for a system with
the equivalent circuit shown in Fig. 5.11(a) [15]. From Fig. 5.13, it can be seen
that, at very low frequencies,
Z = Rs + Rp (5.23)
At very high frequencies,
Z = Rs (5.24)
5.11 THEORY OF CATHODIC PROTECTION
Observing the polarization diagram for the copper–zinc cell in Fig. 5.2, it is clear
that, if polarization of the cathode is continued, using external current, beyond
the corrosion potential to the thermodynamic potential of the anode, both elec-
trodes attain the same potential and no corrosion of zinc can occur. This is the
basis for cathodic protection of metals. Cathodic protection, discussed further in
Chapter 13, is one of the most effective engineering means for reducing the cor-
rosion rate to zero. Cathodic protection is accomplished by supplying an external
current to the corroding metal that is to be protected, as shown in Fig. 5.14.
Current leaves the auxiliary anode (composed of any metallic or nonmetallic
Figure 5.13. Bode magnitude and phase angle plots showing the frequency dependence of
electrochemical impedance for the equivalent circuit model in Fig. 5.11(a) [15]. (Reprinted
with permission of ASM International®. All rights reserved. www.asminternational.org.)
Figure 5.14. Cathodic protection by

impressed current.
conductor), passes through the electrolyte, enters the metal that is to be protected,
and returns to the source of direct current, B. The corroding metal is fully pro-
tected—and the corrosion rate is zero—when it is polarized to the open-circuit
anode potential, also known as the reversible potential, the thermodynamic
potential, and the equilibrium potential. The metal cannot corrode as long as the
current is applied to maintain this potential. The polarization diagram is shown
in Fig. 5.15, where Iappl is the applied current necessary for complete protection.
REFERENCES 79
Figure 5.15. Polarization diagram illustrating principle of cathodic protection.
If the metal is polarized slightly beyond the open-circuit potential, φA, of

the anode, the corrosion rate remains zero. Net current flows from the electro-
lyte to the metal; hence, metal ions cannot enter the solution. Current in excess
of the required does no good, however, and may damage amphoteric metals
and coatings. In practice, therefore, the impressed current is kept close to the
theoretical minimum. Should the applied current fall below that required for
complete protection, some degree of protection nevertheless occurs. For example,
if the corrosion potential is moved from φcorr to a in Fig. 5.15, by applied current
e–b, the corrosion current decreases from Icorr to b. As the applied current e–b
is increased, the potential a moves to more active values, and the corrosion
current b becomes smaller. When a coincides with φA, the corrosion current
becomes zero, and the applied current for complete cathodic protection
equals Iappl.
REFERENCES
1. C. Wagner and W. Traud, Z. Elektrochem. 44, 391 (1938).

2. N. D. Greene, Experimental Electrode Kinetics, Rensselaer Polytechnic Institute, Troy,
NY, 1965; ASTM Standard G5-94 (Reapproved 1999), ASTM, West Conshohocken,
PA.
3. J. O’M. Bockris, A. K. N. Reddy, and M. Gamboa-Aldeco, Modern Electrochemistry, 2nd
edition, Vol. 2A, Fundamentals of Electrodics, Kluwer Academic/Plenum Publishers,
New York, 2000, pp. 1246–1247.
4. M. Stern, J. Electrochem. Soc. 102, 609; ibid., 663 (1955).
5. U. R. Evans, J. Franklin Inst. 208, 45 (1929).
6. F. Mansfeld and R. V. Inman, Corrosion 35 (1), 21 (1979).
7. R. G. Kelly, in Electrochemical Techniques in Corrosion Science and Engineering,

R. G. Kelly, J. R. Scully, D. W. Shoesmith, and R. G. Buchheit, editor, Marcel Dekker,
New York, 2003, pp. 43–45; see also Ref. 3, pp. 1054–1055.
8. M. Stern and A. Geary, J. Electrochem. Soc. 104, 56 (1957).
9. M. Stern and E. Weisert, Am. Soc. Testing Mater. Proc. 59, 1280 (1959).
10. F. Mansfeld and K. Oldham, Corros. Sci. 11, 787 (1971); F. Mansfeld, in Advances in
Corrosion Science and Technology, edited by M. Fontana and R. Staehle, Vol. 6,
Plenum Press, New York, 1976, p. 163.
11. M. Stern, Corrosion 14, 329t (1958).
12. J. R. Scully, in Electrochemical Techniques in Corrosion Science and Engineering,
Marcel Dekker, New York, 2003, p. 125.
13. ASTM G 106-89 (Reapproved 1999), Standard Practice for Verification of Algorithm
and Equipment for Electrochemical Impedance Measurements, ASTM, West Con-
shohocken, PA.
14. G. L. Makar and J. Kruger, Corrosion studies of rapidly solidified magnesium alloys,
J. Electrochem. Soc. 137, 414 (1990).
15. J. R. Scully and R. G. Kelly, Methods for DeterminIng Aqueous Corrosion Reaction
Rates, in ASM Handbook, Vol. 13A, Corrosion: Fundamentals, Testing, and Protection,
ASM International, Materials Park, OH, 2003, p. 73.
GENERAL REFERENCES
E. Barsoukov and J. R. Macdonald, editors, Impedance Spectroscopy, Theory, Experiment,

and Applications, 2nd edition, Wiley, New York, 2005.
J. O’M. Bockris and A. K. N. Reddy, Modern Electrochemistry, 2nd edition, Kluwer Aca-
demic/Plenum Publishers, New York, 2000.
A Century of Tafel’s Equation: A Commemorative Issue of Corrosion Science, Corrosion
Science 47(12), December 2005.
M. Orazem and B. Tribollet, Electrochemical Impedance Spectroscopy, Wiley, New York,
2008.
D. C. Silverman, Practical corrosion prediction using electrochemical techniques, in Uhlig’s
Corrosion Handbook, 2nd edition, R. W. Revie, editor, Wiley, New York, 2000, p.
1179.
W. H. Smyrl, in Comprehensive Treatise of Electrochemistry, Vol. 4, Electrochemical Materi-
als Science, J. O’M. Bockris et al., editors, Plenum Press, New York, 1981, p. 97.
PROBLEMS
1. The potential of an iron electrode when polarized as cathode at 0.001 A/cm2

is −0.916 V versus 1 N calomel half-cell. The pH of the electrolyte is 4.0. What
is the value of the hydrogen overpotential?
PROBLEMS 81
2. The potential of a cathode at which H+ discharges at 0.001 A/cm2 is −0.92 V

versus Ag–AgCl in 0.01 N KCl at 25°C.
(a) What is the cathode potential on the standard hydrogen scale?
(b) If the pH of the electrolyte is 1, what is the value of hydrogen overpotential?
3. The potential of a platinum anode at which oxygen evolves in an electrolyte

of pH 10 is 1.30 V with respect to the saturated calomel electrode. What is
the value of oxygen overpotential?
4. The potential of a copper electrode on which Cu2+ deposits from 0.2 M CuSO4
versus 1 N calomel electrode is −0.180 V. What is the polarization of the
electrode in volts? Is the electrode polarized in the active or noble
direction?
5. Closely separated short-circuited zinc and mercury electrodes are immersed

in deaerated HCl of pH = 3.5. What is the current through the cell if the total
exposed area of each electrode is 10 cm2? What is the corresponding corro-
sion rate of zinc in gmd? (Corrosion potential of zinc versus 1 N calomel
half-cell is −1.03 V.)
6. The corrosion potential of mild steel in a deaerated solution of pH = 2 is

−0.64 V versus saturated Cu–CuSO4 half-cell. The hydrogen overpotential
(volts) for the same steel follows the relation 0.7 + 0.1 log i, where i = A/cm2.
Assuming that approximately all the steel surface acts as cathode, calculate
the corrosion rate in mm/y.
7. Derive an expression for the slope of corrosion rate versus pH for a dilute
cadmium amalgam in a deaerated cadmium ion solution. Neglect concen-
tration polarization and assume that the amalgam is approximately all
cathode.
8. The potential of platinum versus saturated calomel electrode when polarized

cathodically in deaerated H2SO4, pH = 1.0 at 0.01 A/cm2 is −0.334 V and at
0.1 A/cm2 it is −0.364 V. Calculate β and i0 for discharge of H+ on platinum in
this solution.
9. The corrosion rate of iron in deaerated HCl of pH = 3 is 3.0 gmd. Calculate

the corrosion potential of iron in this acid versus 0.1 N calomel electrode.
Assume that the entire iron surface acts as a cathode.
10. The linear polarization slope dφ/dI at low current densities for iron in a cor-
rosive solution equals 2 mV/μA-cm2. Using Eq. (5.8), calculate the corrosion
rate in gmd. Assume βa = βc = 0.1 V.
11. Anodic activation overpotential η for small applied current density i follows
the relation η = ki. Derive the value of k in terms of the exchange current
density i0, assuming βa = βc = 0.1 V.
12. Determine the corrosion potential and corrosion rate of an iron pipe carrying
1 N sulfuric acid at 0.2 m/s at 25°C. Assume that the entire iron surface acts
as cathode, that Tafel slopes are ±0.100 V, and that the exchange current
densities for Fe/Fe2+ and for hydrogen on iron are 10−3 and 10−2 A/m2,
respectively.
13. Determine the corrosion potential and corrosion rate of zinc in 1 N hydro-
chloric acid. Assume that the entire zinc surface acts as cathode, that Tafel
slopes are ±0.100 V, and that the exchange current densities for zinc and for
hydrogen on zinc are 0.1 and 10−4 A/m2, respectively.
14. Show the complex-plane impedance spectra for the following electrochemi-
cal cells:
(a) The cell is represented by a single electrical resistance of value, R (Ω).
(b) The cell is represented by a capacitance of value, C (F).
(c) The cell is represented by an equivalent circuit with a resistance, Rs (Ω), in series
with a capacitance, Cs (F).
(d) The cell is represented by an equivalent circuit with a resistance, Rp (Ω), in paral-
lel with a capacitance, Cp (F).
(e) The cell is represented by the circuit shown in Fig. 5.11(a).
Answers to Problems
1. −0.40 V.
2. (a) −0.58 V; (b) −0.52 V.
3. 0.90 V.
4. −0.188 V; active direction.
5. 2.3 × 10−7 A; 0.0067 gmd.
6. 0.134 mm/y.
7. dicorr/dpH = −2.3(0.059icorr)/β.
8. β = 0.03 V; i0 = 8 × 10−4 A/cm2.
9. −0.719 V.
10. 2.73 gmd.
11. k = 0.0217/i0.
12. −0.17 V (S.H.E.); 0.58 mm/y.
13. −0.53 V (S.H.E.); 29.9 mm/y.
6
PASSIVITY
6.1 DEFINITION
A passive metal is one that is active in the Emf Series, but that corrodes never-
theless at a very low rate. Passivity is the property underlying the useful natural
corrosion resistance of many structural metals, including aluminum, nickel, and
the stainless steels. Some metals and alloys can be made passive by exposure to
passivating environments (e.g., iron in chromate or nitrite solutions) or by anodic
polarization at sufficiently high current densities (e.g., iron in H2SO4).
As early as the eighteenth century, it was observed that iron reacts rapidly
in dilute HNO3, but is visibly unattacked by concentrated HNO3 [1]. Upon
removing iron from the concentrated acid and immersing it into the dilute acid,
a temporary state of corrosion resistance persists. In 1836, Schönbein [2] defined
iron in the corrosion-resistant state as “passive.” He also showed that iron could
be made passive by anodic polarization. Around the same time, Faraday [3]
performed several experiments showing, among other things, that a cell made up
of passive iron coupled to platinum in concentrated nitric acid produced little or
no current, in contrast to the high current produced by amalgamated zinc coupled
to platinum in dilute sulfuric acid. Although passive iron corrodes only slightly
in concentrated HNO3, and similarly amalgamated zinc corrodes only slightly in

83
84 PASSIVIT Y
dilute H2SO4, Faraday emphasized that a low corrosion rate is not alone a
measure of passivity. Instead, he stated, the magnitude of current produced in
the cell versus platinum is a better criterion, for on this basis iron is passive, but
not zinc. This, in essence, defined a passive metal, as we do today, as one that is
appreciably polarized by a small anodic current. Later investigators deviated
from this definition, however, and also called metals passive if they corrode only
slightly despite their pronounced tendency to react in a given environment. This
usage brought about two definitions of passivity:
Definition 1. A metal is passive if it substantially resists corrosion in a given

environment resulting from marked anodic polarization.
Definition 2. A metal is passive if it substantially resists corrosion in a given
environment despite a marked thermodynamic tendency to react.
C. Wagner [4] offered an extension of Definition 1, the essence of which is the

following: A metal is passive if, on increasing the electrode potential toward more
noble values, the rate of anodic dissolution in a given environment under steady-
state conditions becomes less than the rate at some less noble potential. Alter-
natively, a metal is passive if, on increasing the concentration of an oxidizing
agent in an adjacent solution or gas phase, the rate of oxidation, in absence of
external current, is less than the rate at some lower concentration of the oxidizing
agent. These alternative definitions are equivalent under conditions where the
electrochemical theory of corrosion applies.
Thus, lead immersed in sulfuric acid, or magnesium in water, or iron in
inhibited pickling acid, would be called passive by Def. 2 based on low corrosion
rates, despite pronounced corrosion tendencies; but these metals are not passive
by Def. 1. Their corrosion potentials are relatively active, and polarization is not
pronounced when they are made the anode of a cell.
Examples of metals that are passive under Definition 1, on the other hand,
include chromium, nickel, molybdenum, titanium, zirconium, the stainless steels,
70%Ni–30%Cu alloys (Monel), and several other metals and alloys. Also included
are metals that become passive in passivator solutions, such as iron in dissolved
chromates. Metals and alloys in this category show a marked tendency to polarize
anodically. Pronounced anodic polarization reduces observed reaction rates, so
that metals passive under Definition 1 usually conform as well to Definition 2
based on low corrosion rates. The corrosion potentials of metals passive by Defi-
nition 1 approach the open-circuit cathode potentials (e.g., the oxygen electrode);
hence, as components of galvanic cells, they exhibit potentials near those of the
noble metals.
6.2 CHARACTERISTICS OF PASSIVATION AND

THE FLADE POTENTIAL
Suppose iron is made anode in 1N H2SO4 and is arranged so that, as the potential
is gradually increased, the corresponding polarizing current reaches the value
CHAR ACTERISTICS OF PASSIVATION AND THE FL ADE POTENTIAL 85
required to maintain the prevailing potential with respect to a reference elec-

trode. In the laboratory, this is usually accomplished using a potentiostat, which
controls the potential between the “working” electrode and the reference elec-
trode by automatically adjusting the current between the “working” electrode
and an inert electrode, usually platinum, that is called the “auxiliary” or “counter”
electrode. The resulting polarization curve, shown in Fig. 6.1 [5], is called a
potentiostatic polarization curve.
Galvanostatic polarization is an alternative to potentiostatic polarization. In
galvanostatic polarization measurements, the current between working and
counter electrodes is controlled, and the potential between working and refer-
ence electrodes is automatically adjusted to the value required to maintain the
current. Galvanostatic measurements can be made using, for example, the circuit
shown in Fig. 5.3(a) in Section 5.3. The galvanostatic polarization curve for iron
in 1N H2SO4 is shown in Fig. 6.2.
The potentiostatic polarization curve provides considerably more informa-
tion about passivity than does the galvanostatic curve.
Referring to Fig. 6.1, iron is active at small current densities and corrodes
anodically as Fe2+ in accord with Faraday’s law. As current increases, a partially
insulating film forms over the electrode surface, composed probably of FeSO4.
At a critical current density, icritical, of about 0.2 A/cm2 (higher on stirring or on
lowering pH of the environment), the current suddenly drops to a value orders
of magnitude lower, called the passive current density, ipassive. At this point, the
thick insulating film dissolves, being replaced by a much thinner film, and iron
becomes passive. The value of ipassive decreases with time, diminishing to about
Figure 6.1. Potentiostatic anodic polarization curve for iron in 1N H2SO4.

86 PASSIVIT Y
Figure 6.2. Galvanostatic anodic polarization curve for iron in 1N H2SO4.
7 μA/cm2 in 1N H2SO4. In other electrolytes, ipassive may be higher or lower than

in 1N H2SO4. The true critical current density for achieving passivity of iron
in absence of an insulating reaction-product layer is estimated to be about 10–
20 A/cm2, as shown by short-time current–pulse measurements.
On further gradual change of the potential, the current density remains at
the above low value, and the corrosion product is now Fe3+. At about 1.2 V, the
equilibrium oxygen electrode potential is reached, but oxygen is not evolved
appreciably until the potential exceeds the equilibrium value by several tenths
of a volt (oxygen overpotential). The increased current densities in the region
labeled “transpassive” represent O2 evolution plus Fe3+ formation.
When the applied potential is removed, passivity decays within a short time
in the manner shown in Fig. 6.3. The potential first changes quickly to a value
still noble on the hydrogen scale, and then it changes slowly for a matter of
seconds to several minutes. Finally, it decays rapidly to the normal active poten-
tial of iron. The noble potential arrived at just before rapid decay to the active
value was found by Flade [6] to be more noble the more acid the solution in
which passivity decayed. This characteristic potential, φF, was later called the
Flade potential, and Franck established it to be a linear function of pH [7]. His
measurements in acid media, combined with later data by others, provide the
relation at 25°C:
φ F ( volts, S.H.E.) = +0.63 − 0.059 pH (6.1)
This reproducible Flade potential and its 0.059 pH dependence is characteristic

of the passive film on iron. A similar potential–pH relation is found for the
passive film on chromium, for Cr–Fe alloys,* and for nickel, for which the stan-
*When activated cathodically, the Flade potential of chromium and stainless steels follows the
relation n(0.059 pH), where n may be as high as 2. For self-activation, n is 1 [8].
CHAR ACTERISTICS OF PASSIVATION AND THE FL ADE POTENTIAL 87
Figure 6.3. Decay of passivity of iron in 1N H2SO4 showing Flade potential, ϕF.
dard Flade potentials (pH = 0) are less noble than for iron, in accord with more
stable passivity.
Stability of passivity is related to the Flade potential, assuming the following
schematic reaction to take place during anodic passivation:
M + H 2 O → O ⋅ M + 2 H + + 2e − (6.2)
where −φF is the potential for the reaction, and O·M refers to oxygen in the
passive film on metal M whatever the passive film composition and structure may
be. The amount of oxygen assumed to be combined with M has no effect on
present considerations. It follows, as observed, that
0.059
φ F = φF + log (H + )2 = φF − 0.059 pH (6.3)
2
The positive value of φF for iron (0.63 V) indicates considerable tendency for
the passive film to decay [reverse reaction of (6.2)], whereas an observed negative
value of φF = −0.2 V for chromium indicates conditions more favorable to
passive-film formation and, hence, greater stability of passivity. The value of φF
for nickel is 0.2 V. For chromium–iron alloys, values range from 0.63 V for pure
iron to increasingly negative values as chromium is alloyed, changing most rapidly
in the range 10–15% chromium and reaching about −0.1 V at 25% chromium.
The corresponding φF values are shown in Fig. 6.4.
88 PASSIVIT Y
Figure 6.4. Standard Flade potentials for chromium–iron alloys and chromium [7–9].
The potential (P in Fig. 6.1) at which passivity of iron initiates (passivating

potential) approximates, but is not the same as, the Flade potential because of
IR drop through the insulating layer first formed and because the pH of the
electrolyte at the base of pores in this layer differs from that in the bulk of
solution (concentration polarization). These effects are absent on decay of
passivity.
6.3 BEHAVIOR OF PASSIVATORS*
The same Flade potential is obtained whether iron is passivated by concentrated

nitric acid or is anodically polarized in sulfuric acid, indicating that the passive
film is essentially the same in both instances. In fact, when iron is passivated by
immersion in solutions of passivators, whether chromates (CrO2− 4 ), nitrites
(NO−2 ), molybdates (MoO2− 2− 2−
4 ), tungstates (WO4 ), ferrates ( FeO4 ), or pertechne-
tates (TcO−4 ), the corresponding Flade potentials are close to values obtained
*See also Chapter 17.

BEHAVIOR OF PASSIVATORS 89
otherwise [10, 11]. Hence, it can be concluded that the passive film on iron is
essentially the same regardless of the passivation process. The amount of passive-
film substance, as determined by coulometric and other measurements, is approx-
imately 0.01 C/cm2 in all cases. Passivation proceeds by an electrochemical
mechanism, with some exceptions discussed later.
The standard Flade potential of iron passivated by chromates (φF = 0.54 V)
is less noble than for iron passivated by HNO3 (φF = 0.63 V). One explanation
[11] is that chromates adsorb on the passive film more strongly than do nitrates,
thereby reducing the overall free energy of the system and increasing the stability
of the passive film. Other passivators presumably adsorb similarly, but with dif-
fering energies of adsorption.
Passivators are reduced at cathodic areas at a current density equivalent to
a true current density at anodic areas equaling or exceeding icritical (10–20 A/cm2)
for passivation of iron. The passivator is reduced over a large cathodic area of
the metal surface to an extent not less than that necessary to form a chemically
equivalent passive film at small residual anodic areas. The small passive areas,
in turn, adsorb passivator, thereby becoming noble to adjoining passive or non-
passive areas, causing passivity to spread. When the passive film is complete, it
acts as cathode over its entirety, and further reduction of passivator proceeds
at a much slower rate, equivalent to the rate of continuous passive film break-
down, or to ipassive. Since breakdown is accelerated by presence of chlorides
and by elevated temperatures, consumption of passivator is also increased
correspondingly.
Passivators as a group are inorganic oxidizing agents that have the unique
property of reacting only slowly when in direct contact with iron, but they are
reduced more rapidly by cathodic currents. For this reason, they can adsorb first
on the metal surface, with each site of adsorption adding to the cathodic area.
The higher the concentration of passivator, the more readily it adsorbs, and the
smaller the residual anodic areas become; this situation obviously favors increased
anodic polarization and ultimately passivation. It requires about 0.5–2 h for the
passive film to form completely when iron is immersed in 0.1% K2CrO4, with the
shorter time being characteristic of aerated solution while the longer time is
typical of deaerated solution [12, 13].
6.3.1 Passivation of Iron by HNO3

In nitric acid, the cathodic depolarizer (passivator) is nitrous acid, HNO2. This
must form first in sufficient quantity by an initial rapid reaction of iron with
HNO3. As nitrous acid accumulates, anodic current densities increase, eventually
reaching icritical. Passivity is then achieved, and the corrosion rate falls to the com-
paratively low value of about 2 gmd [14].
If urea is added to concentrated HNO3, passivation is interrupted because
urea reacts with nitrous acid in accord with
(NH 2)2CO + 2 HNO2 → 2 N 2 + CO2 + 3H 2O (6.4)

90 PASSIVIT Y
thereby decreasing the nitrous acid concentration. The rate of reaction is,
nevertheless, sufficiently below that of HNO2 production so that passivity can
still occur, although periodic breakdown and formation of the passive film usually
result.
Hydrogen peroxide added to concentrated nitric acid also causes periodic
breakdown and formation of passivity, probably by oxidizing HNO2 to HNO3
[14]. The peroxide, of itself, is not as efficient a cathodic depolarizer as HNO2,
and hence the passive film in its presence can repair itself only when the moment-
ary surface concentration of HNO2 formed by reaction of iron with HNO3 is
sufficiently high. After passivity is achieved, the surface concentration of HNO2
is diminished by reaction with peroxide below that needed to maintain passivity,
whereupon the cycle is repeated.
If iron is first immersed in dilute chromate solution for several minutes, it
remains passive in concentrated nitric acid without the initial reaction to form
HNO2. The passive film is preformed by chromate, and nitrous acid is no longer
necessary as depolarizer to reach icritical, but is needed only in concentration suf-
ficient to maintain the film already present.
6.4 ANODIC PROTECTION AND TRANSPASSIVITY
The electrochemical nature of the passivation process is the basis on which

anodic polarization leads to passivation. The anodic polarization that is required
for passivation can be achieved by applying current or by increasing either the
cathodic area or the cathodic reaction rate. High-carbon steels, for example—
which contain areas of cementite (Fe3C) that act as cathodes—are more readily
passivated by concentrated nitric acid than is pure iron. For this reason, nitrating
mixtures of sulfuric and nitric acids are best stored or shipped in drums of steel
of the highest carbon content consistent with required mechanical properties.
Similarly, stainless steels that may lose passivity in dilute sulfuric acid retain their
corrosion resistance if alloyed with small amounts of more noble constituents of
low hydrogen overpotential, or of low overpotential for cathodic reduction of
dissolved oxygen, such as Pd, Pt, or Cu [15]. The polarization diagram correspond-
ing to increased passivity by low overpotential cathodes is shown in Fig. 6.5, and
the corresponding improved corrosion resistance to sulfuric acid is shown in
Fig. 6.6.
Because titanium, unlike 18–8 stainless steel, has a low critical current density
for passivity in chlorides as well as in sulfates, passivity in boiling 10% HCl is
made possible by alloying titanium with 0.1% Pd or Pt [16]. Pure titanium, on
the other hand, corrodes in the same acid at very high rates (see Fig. 25.2, Section
25.3).
Based on the same principle, the corrosion resistance of metals and alloys
with polarization curves having active–passive transitions can be greatly improved
by an impressed anodic current initially equal to or greater than the critical
current for passivity. The potential of the metal moves into the passive region
ANODIC PROTEC TION AND TR ANSPASSIVIT Y 91
Figure 6.5. Polarization diagram for metal that is either active or passive, depending on
overvoltage of cathodic areas (differing cathodic reaction rates).
Figure 6.6. Corrosion rates in sulfuric acid of 18–8 stainless steel alloyed with copper or pal-
ladium, 360-h test, 20°C [15].
(Fig. 6.1), so that the current density and accompanying corrosion rate corre-
spond to the low value of ipassive. This process is called anodic protection (see
Section 13.9) because the current flow is in the direction opposite to that which
is used in cathodic protection. Whereas cathodic protection can, in principle, be
applied to both passive and nonpassive metals, anodic protection is applicable
only to metals that can be passivated when anodically polarized (see Definition
1, Section 6.1).
92 PASSIVIT Y
If the cathodic polarization curves of Fig. 6.5 intersect the anodic curve at a
still more noble potential, within the transpassive region, the corrosion rate of,
for example, stainless steel, is greatly increased over the corrosion rate at less
noble potentials within the passive region, and the corrosion products become
Cr2O72− and Fe3+. Transpassivity occurs not only with stainless steels, but also
with chromium, for which the potential for the reaction
Cr2 O72 − + 14 H + + 12e − → 2Cr + 7 H 2 O φ = 0.30 V (6.5)
is less noble than the potential for the oxygen evolution reaction
O2 + 4 H + + 4e − → 2 H 2 O φ = 1.23 V (6.6)
Appreciable corrosion in the transpassive region does not occur for iron in sul-
furic acid (oxygen evolution is the primary reaction), but increased corrosion
does occur in alkaline solutions that favor formation of ferrate, FeO2−
4 . Transpas-
sivity accounts for an observed increase of corrosion rate with time for 18–8
stainless steels in boiling concentrated nitric acid, in which corrosion products
accumulate, in particular Cr2O72− , and move the corrosion potential into the
transpassive region.
6.5 THEORIES OF PASSIVITY
There are two commonly expressed points of view regarding the composition
and structure of the passive film. The first holds that the passive film (Definition
1 or 2) is always a diffusion-barrier layer of reaction products—for example,
metal oxide or other compound that separates metal from its environment and
that decreases the reaction rate. This theory is sometimes referred to as the
oxide-film theory.
The second holds that metals passive by Definition 1 are covered by a che-
misorbed film—for example, of oxygen. Such a layer displaces the normally
adsorbed H2O molecules and decreases the anodic dissolution rate involving
hydration of metal ions. Expressed another way, adsorbed oxygen decreases the
exchange current density (increases anodic overvoltage) corresponding to the
overall reaction M → Mz+ + ze−. Even less than a monolayer on the surface is
observed to have a passivating effect [17]; hence, it is suggested that the film
cannot act primarily as a diffusion-barrier layer. This second point of view is
called the adsorption theory of passivity.
There is no question on either viewpoint that a diffusion-barrier film is the
basis of passivity of many metals that are passive only by Definition 2. Examples
of protective films that isolate the metal from its environment are (a) a visible
lead sulfate film on lead immersed in H2SO4 and (b) an iron fluoride film on steel
immersed in aqueous HF.
THEORIES OF PASSIVIT Y 93
For metals that are passive by Definition 1, based on marked anodic polar-
ization, the films are usually invisible, about 2 to 3 nm thick. Metals and alloys in
this category have been the source of extended debate and discussion on the
mechanism of passivity over the past 150 years. If the surface is abraded, local
high temperatures generated at the surface produce a detectable oxide, but this
is not the passive film.
Low-energy electron-diffraction (LEED) techniques are used to detect
adsorbed films, including those responsible for passivity. Surface analytical tech-
niques that can be used to study films on metals include Auger electron spec-
troscopy (AES), X-ray photoelectron spectroscopy (XPS), secondary ion mass
spectrometry (SIMS), and others [18, 19]. Using these advanced techniques, evi-
dence has been developed to show that the passive film formed on iron in borate
solution is an anhydrous, crystalline spinel with a “γ-Fe2O3/Fe3O4-like” structure
[19].
The adsorption theory derives support from the fact that most of the metals
that are passive by Definition 1 are transition metals of the periodic table; that
is, they contain electron vacancies or uncoupled electrons in the d shells of the
atom. The uncoupled electrons account for strong bond formation with compo-
nents of the environment, especially O2, which also contains uncoupled electrons
(hence its slight paramagnetic susceptibility) resulting in electron-pair or cova-
lent bonding supplementary to ionic bonding. Furthermore, transition metals
have high heats of sublimation compared to nontransition metals, a property that
favors adsorption of the environment because metal atoms tend to remain in
their lattice, whereas oxide formation requires metal atoms to leave their lattice.
The characteristic high energies for adsorption of oxygen on transition metals
correspond to chemical-bond formation; hence, such films are called chemisorbed
in contrast to lower-energy films, which are called physically adsorbed. On the
nontransition metals, such as copper and zinc, oxides tend to form immediately,
and any chemisorbed films on the metal surface are short-lived. On transition
metals, the initially chemisorbed oxygen is generally more stable thermodynami-
cally than is the metal oxide [20]. This situation reverses for multilayer adsorbed
oxygen films (lower energy of bonding to the metal) that revert in time to metal
oxides. But such oxides are less important in accounting for passivity than the
chemisorbed films that form initially and continue to form on metal exposed at
pores in the oxide.
The adsorption theory emphasizes that the observed Flade potential of
passive iron is too noble by about 0.6 V to be explained by any of the known iron
oxides in equilibrium with iron. Observed values of the Flade potential are con-
sistent with a chemisorbed film of oxygen on the surface of iron, the correspond-
ing potential of which is calculated (see Problem 2 in Chapter 6) using the
observed heat and estimated entropy of adsorption of oxygen on iron in accord
with the reaction [21]
O2 ⋅ Oads on Fe + 6 H + + 6e − → 3H 2O + Fe surface φcalc = 0.57 V (6.7)

94 PASSIVIT Y
The measured chemical equivalents of passive-film substance (about 0.01 C/cm2)

correspond (roughness factor = 4) to one atomic layer of oxygen atoms
(r = 0.07 nm) over which one layer of oxygen molecules (r = 0.12 nm) is
chemisorbed; hence, the adsorbed passive film may be represented above by
O2·Oads on Fe. The value of the Flade potential, as cited in Eq. (6.1), corresponds to
φobs = 0.63 V , which is in reasonable agreement with the calculated value, 0.57 V.
The agreement is still better if account is taken of adsorbed water displaced from
the metal surface by the passive film during the passivation reaction, this displace-
ment presumably involving a greater free energy change than the adsorption of
water on the passive film itself [8].
Further confirming evidence that the passive film on iron contains oxygen in
a higher-energy state than corresponds to any iron oxide is obtained from the
ability of the passive film to oxidize chromite, CrO−2, to chromate, CrO2− 4 , in
NaOH solution [14]. This oxidation does not occur with active iron. The maximum
oxidizing capacity corresponds to 0.012 C/cm2 of passive-film substance in accord
with the reaction
O2⋅Oads on Fe + Fe + OH − + CrO−2 + H 2O → Fe(OH)3 + CrO24−

(6.8)
ΔG = −138,000 J
Calculations show that the same reaction will not go for chromium or the stain-
less steels, on which the passive film is more stable.
On breakdown of passivity, 0.01 C/cm2 of adsorbed oxygen on iron reacts
with underlying metal in accord with
O2 ⋅ Oads on Fe + 2 Fe + 3H 2O → 2 Fe(OH)3 or Fe2O3 ⋅ 3H 2O (6.9)
A layer of Fe2O3 (mol. wt. = 159.7; d = 5.12 g/cm3) is formed equal to a minimum
of (0.01 × 159.7)/(6 × 96,500 × 5.12) = 5.4 nm thick (based on apparent area). The
hydrated oxide would be thicker. This value compares in magnitude with mea-
sured values for the thickness of the decomposed passive film (2.5–10 nm). It is
the decomposed passive film that is presumably isolated in experiments designed
to remove the passive film from iron.
According to the adsorption theory, passivity of chromium and the stainless
steels, because of their pronounced affinity for oxygen, can occur by direct che-
misorption of oxygen from the air or from aqueous solutions, and the equivalents
of oxygen so adsorbed were found [22] to be of the same order of magnitude as
the equivalents of passive film formed on iron when passivated either anodically,
by concentrated nitric acid, or by exposure to chromates. Similarly, oxygen in air
can adsorb directly on iron and passivate it in aerated alkaline solutions, or
also in near-neutral solutions if the partial pressure of oxygen is increased
sufficiently.
THEORIES OF PASSIVIT Y 95
6.5.1 More Stable Passive Films with Time

Flade observed that the longer iron remains in concentrated nitric acid, the
longer the passive film remains stable when the iron is subsequently immersed
in sulfuric acid [6]. In other words, the film is stabilized by continued exposure
to the passivating environment. Similarly, Frankenthal [17] noted that the film
on 24% Cr–Fe thickened and became more resistant to cathodic reduction when
the alloy was passivated for longer times in 1N H2SO4 at potentials noble to the
passivating potential (P in Fig. 6.1), although less than monolayer quantities of
oxygen (measured coulometrically) suffice to passivate this alloy in this solution.
The observed stabilizing effect is likely the result of positively charged metal
ions entering the adsorbed layers of negatively charged oxygen ion and mole-
cules, with the coexisting opposite charges tending to stabilize the adsorbed film.
Low-energy electron-diffraction data for nickel single crystals [23]. indicate that
the first-formed adsorbed film consists of a regular array of oxygen and nickel
ions located in the same approximate plane of the surface. This initial adsorbed
layer is found to be more stable thermally than the oxide, NiO. At increasing
oxygen pressures, several adsorbed layers, probably consisting of O2, form on
top of the first layer and result in an amorphous film. Additional metal ions in
time succeed in entering such a film, particularly in the noble potential range,
becoming a mobile species within the adsorbed oxygen layer. Protons from the
aqueous environment are also incorporated. Okamoto and Shibata [24], for
example, showed that the passive film on 18–8 stainless steel contains H2O.
Eventually, the stoichiometric oxide is nucleated at favorable sites on the metal
surface, and such nuclei then grow laterally to form a uniform oxide film; but
the adsorbed (passive) film remains intact at pores in the oxide. A schematic
structure of the first-formed adsorbed passive film is shown in Fig. 6.7 [20]. The
initial passive film grows into a multilayer adsorbed M·O·H structure, which can
Figure 6.7. Schematic structure of initial passive films containing less or more than mono-
layer amounts of adsorbed oxygen, along with schematic structure of a thicker passive film
containing additional metal ions and protons in nonstoichiometric amounts.
96 PASSIVIT Y
be considered to be an amorphous nonstoichiometric oxide. It differs markedly

in protective properties from the stoichiometric oxide into which it may eventu-
ally convert.
6.5.2 Action of Chloride Ions and Passive–Active Cells

Chloride ions—and, to a lesser extent, other halogen ions—break down passivity
or prevent its formation in iron, chromium, nickel, cobalt, and the stainless steels.
From the perspective of the oxide-film theory, Cl− penetrates the oxide film
through pores or defects easier than do other ions, such as SO2− 4 . Alternatively,
Cl− may colloidally disperse the oxide film and increase its permeability.
On the other hand, according to the adsorption theory, Cl− adsorbs on the
metal surface in competition with dissolved O2 or OH−. Once in contact with the
metal surface, Cl− favors hydration of metal ions and increases the ease with
which metal ions enter into solution, opposite to the effect of adsorbed oxygen,
which decreases the rate of metal dissolution. In other words, adsorbed chloride
ions increase the exchange current (decrease overvoltage) for anodic dissolution
of the above-mentioned metals over the value prevailing when oxygen covers the
surface. The effect is so pronounced that iron and the stainless steels are not
readily passivated anodically in solutions containing an appreciable concentra-
tion of Cl−. Instead, the metal continues to dissolve at high rates in both the active
and passive potential ranges.
Breakdown of passivity by Cl− occurs locally rather than generally, with the
preferred surface sites being determined perhaps by small variations in the
passive-film structure and thickness. Minute anodes of active metal are formed
surrounded by large cathodic areas of passive metal. The potential difference
between such areas is 0.5 V or more, and the resulting cell is called a passive–
active cell. High current densities at the anode cause high rates of metal penetra-
tion, accompanied by cathodic protection of the metal area immediately
surrounding the anode. This fixes the anode in place and results in pitting cor-
rosion. Also, the greater the current flow and cathodic protection at any pit, the
less likely it is that another pit will initiate nearby; hence, the observed number
of deep pits per unit area is usually less than that of smaller shallow pits. It is
evident, because of the possibility of passive–active cell formation, that deep
pitting is much more common with passive metals than with nonpassive
metals.
Halogen ions have less effect on the anodic behavior of titanium, tantalum,
molybdenum, tungsten, and zirconium. Passivity of these metals may continue in
media of high chloride concentration, in contrast to the behavior of iron, chro-
mium, and Fe–Cr alloys, which lose passivity. This behavior is sometimes
explained by formation of insoluble protective Ti, Ta, Mo, etc., basic chloride
films. However, the true situation is probably related to the high affinity of these
metals for oxygen, making it more difficult for Cl− to displace oxygen of the
passive film, in accord with the noble critical potentials of these metals above
which pitting is initiated, if pitting occurs at all.
CRITICAL PIT TING POTENTIAL 97
6.6 CRITICAL PITTING POTENTIAL
When iron is anodically polarized potentiostatically in 1N H2SO4 to which sodium

chloride is added (>3 × 10−4 moles/liter), the apparent transpassive region is
shifted to lower potentials. However, instead of oxygen being evolved, the metal
corrodes locally with formation of visible pits. Similarly, if 18–8 stainless steel is
anodically polarized in 0.1N NaCl within the lower passive region, the alloy
remains passive, analogous to its behavior in Na2SO4 solution, no matter how
long the time. But above a critical potential, called the critical pitting potential
(CPP), there is a rapid increase in the current, accompanied by random formation
of pits (Fig. 6.8). The CPP for 18–8 moves toward less noble values as the Cl−
concentration increases, and it moves toward more noble values with increasing
pH and with lower temperatures [25]. The CPP is also moved in the noble direc-
tion by adding extraneous salts to the NaCl solution—for example, Na2SO4,
NaNO3, and NaClO4 (Fig. 6.8). If sufficient extraneous salt is added to shift the
CPP to a value more noble than the prevailing corrosion potential, pitting does
not occur at all on exposure of the stainless steel to the aqueous salt mixture.
The added salts under these conditions become effective inhibitors. Addition of
3% NaNO3 to 10% FeCl3, for example, has prevented pitting of 18–8 stainless
steel or any appreciable weight loss for a period of more than 25 years, whereas
in the absence of NaNO3 the alloy is observed to corrode by pitting within hours
[26]. The 3% NaNO3 addition moves the CPP to a value more noble than the
open-circuit cathode potential or the reversible potential for Fe3+ + e− → Fe2+.
Figure 6.8. Potentiostatic polarization curves for 18–8 stainless steel in 0.1M NaCl showing
increasingly noble values of the critical pitting potential with additions of Na2SO4, 25°C.
98 PASSIVIT Y
TABLE 6.1. Critical Pitting Potentials in 0.1N NaCl at 25°C
Potential (V, s.h.e.) Reference
Ala −0.37 [29]

Ni 0.28 [30]
Zr 0.46 [31]
18–8 stainless steelb 0.26 [30]
30% Cr–Fe 0.62 [30]
12% Cr–Fe 0.20 [30]
Cr >1.0 [32]
Ti >1.0 (1N NaCl) [33]
≈1.0 (1N NaCl, 200°C)
a
φcritical (V, s.h.e.) = −0.124 log (Cl−) − 0.504, where (Cl−) is activity of Cl−.
b
φcritical (V, s.h.e.) = −0.088 log (Cl−) + 0.168.
Along the same lines, Leckie [27] polarized 18–8 stainless steel at a constant 0.1 V
below the CPP in 0.1N NaCl for 14 weeks without observable pitting.
CPPs of several metals in 0.1N NaCl are listed in Table 6.1, values of which
were derived from anodic polarization curves. Most of the data were obtained
by allowing 5 minutes or more at a given potential and observing whether the
resultant current increases or decreases with time. The CPP is the most noble
potential for which the current decreases or remains constant; it is usually con-
firmed by holding the potential at the critical value for 12 hours or more and
observing absence of pits under a low-power microscope.
CPPs can be used to compare the relative susceptibility of different alloys to
pitting corrosion; however, because CPPs are the result of short-term experi-
ments, they should be used with caution in predicting immunity to pitting corro-
sion in long-term service. Pitting corrosion has been reported in long-term
exposure at potentials below the CPP [28].
It is observed that an increase in the chromium content of stainless steels—
and, to a lesser extent, an increase of nickel content—shifts the critical potential
to more noble values, corresponding to increased resistance to pitting [30, 31].
The noble critical potentials for chromium and titanium [more noble than the
oxygen electrode potential in air (0.8 V) in accord with O2(0.2 atm) + 4H+ (10−7)
+ 4e− → 2H2O] indicate that these metals are not expected to undergo pitting
corrosion in aerated saline media at normal temperatures. At elevated tempera-
tures and high Cl− concentrations, however, the critical potentials become more
active, so that pitting of titanium, for example, is observed in concentrated hot
CaCl2 solution despite its immunity to pitting in seawater.
The critical potential has been explained, from one point of view, as that
value needed to build up an electrostatic field within the passive or oxide film
sufficient to induce Cl− penetration to the metal surface [34]. Other anions may
also penetrate the oxide, depending on size and charge, contaminating the oxide
and making it a better ionic conductor favoring oxide growth. Eventually, either
CRITICAL PIT TING TEMPER ATURE 99
the oxide is undermined by condensation of migrating vacancies, or cations of

the oxide undergo dissolution at the electrolyte interface; in both cases, pitting
results. The induction period preceding pitting is related to the time required for
the supposed penetration of Cl− through the oxide film.
Alternatively, the critical potential is explained in terms of competitive
adsorption of Cl− with oxygen of the passive film (adsorption theory). The metal
has typically greater affinity for oxygen than for Cl−, but, as the potential is made
more noble, the concentration of Cl− ions at the metal surface increases, eventu-
ally reaching a value that allows Cl− to displace adsorbed oxygen. The observed
induction period is the time required for successful competitive adsorption at
favored sites of the metal surface, as well as time for penetration of the passive
film. Adsorbed Cl−, compared to adsorbed oxygen, results in lower anodic over-
voltage for metal dissolution, which accounts for a higher rate of corrosion at
any site where the exchange has taken place. Extraneous anions, such as NO3−
or SO2− 4 , which do not break down the passive film or cause pitting, compete with
Cl− for sites on the passive surface, making it necessary to shift the potential to
a still more noble value in order to increase Cl− concentration sufficient for suc-
cessful exchange with adsorbed oxygen.*
Below the CPP, Cl− cannot displace adsorbed oxygen so long as the passive
film remains intact; hence, pitting is predicted not to occur. Should passivity
break down because of factors other than those described [e.g., reduced oxygen
or depolarizer concentration at a crevice (crevice corrosion), or cathodic polar-
ization of local shielded areas], pitting could then initiate independent of whether
the overall prevailing potential is above or below the critical value. But under
conditions of uniform passivity for the entire metal surface, application of
cathodic protection to avoid pitting corrosion need only shift the potential of the
metal below the critical value. This is in contrast to the usual procedure of
cathodic protection, which requires polarization of a metal to the much more
active open-circuit anode potential.
The relation between minimum anion activity necessary to inhibit pitting of
18–8 stainless steel in a solution of given Cl− activity follows the relation log (Cl−)
= k log (anion) + const. The same relation applies to inhibition of pitting of alu-
minum. The equation can be derived assuming that ions adsorb competitively in
accord with the Freundlich adsorption isotherm [26].
6.7 CRITICAL PITTING TEMPERATURE
Pitting tendency increases with increasing temperature, with the result that the
critical pitting potential decreases as temperature increases. The critical pitting
temperature (CPT) is defined as the temperature below which an alloy does not
*Rosenfeld and Maximtschuk [Z. Physik. Chem. (D.D.R.) 215, 25 (1960)] reported a quantitative
study showing that the more noble the applied potential, the more Cl− in aqueous solution adsorbs
on metallic Cr, and they also showed that added SO 4 or OH− displaces adsorbed Cl−.
2−
100 PASSIVIT Y
pit regardless of potential and exposure time. CPTs are usually measured in an
aggressive Cl− solution, such as a FeCl3 solution. The CPT can be used to evaluate
and compare pitting susceptibilities of alloys [35].
6.8 PASSIVITY OF ALLOYS
Several metals, such as chromium, are naturally passive when exposed to the
atmosphere, and they remain bright and tarnish-free for years, in contrast to iron
and copper, which corrode or tarnish in short time. It is found that the passive
property of chromium is conferred on alloys of Cr–Fe, provided that ≥12 wt.%
Cr is present. Iron-base alloys containing a minimum of 12 wt.% Cr are known
as the stainless steels.
Typical corrosion, potential, and critical-current density behavior of Cr–Fe
alloys is shown in Figs. 6.9–6.11. Note in Fig. 6.11 that icritical for passivation of
Cr–Fe alloys at pH 7 reaches a minimum at about 12% Cr in the order of 2 μA/
cm2. This value is so low that corrosion currents in aerated aqueous media
easily achieve or exceed this value, illustrating why >12% Cr–Fe alloys are self-
passivating. In addition, the passive film becomes more stable with increasing
chromium content of the alloy.
Several other alloy systems exhibit critical compositions for passivity, as was
first described by Tammann [36]. Examples of approximate critical compositions
Figure 6.9. Corrosion rates of chromium–iron alloys in intermittent water spray at room
temperature. [Reprinted with permission from W. Whitman and E. Chappell, Ind. Eng. Chem.
18, 533 (1926). Copyright 1926, American Chemical Society.]
PASSIVIT Y OF ALLOYS 101
Figure 6.10. Potentials of chromium–iron alloys in 4% NaCl. [Reprinted with permission from
H. Uhlig, N. Carr, and P. Schneider, Trans. Electrochem. Soc. 79, 111 (1941). Copyright 1941,
The Electrochemical Society.]
Figure 6.11. Critical current densities for passivation of chromium–iron alloys in deaerated
3% Na2SO4 at pH 3 and 7, 25°C [8]; data in 10% H2SO4, room temperature, are from R. Olivier,
Proceedings, 6th Meeting, International Committee on Electrochemistry, Thermodynamics,
and Kinetics, Poitiers, Butterworths, London, 1955, p. 314.
102 PASSIVIT Y
determined from plots of icritical versus alloy composition are 35% Ni–Cu, 15%
Mo–Ni, 8%Cr–Co, and 14% Cr–Ni. Critical alloy compositions for passivity have
also been observed in three- and four-component alloys—for example, Fe–Cr–
Ni–Mo [37], Fe–Ni–Mo, and Cr–Ni–Fe [38].
Critical compositions based on icritical values are not sensitive to the pH of the
electrolyte in which the polarization data are measured (Fig. 6.11). On the other
hand, critical compositions based on corrosion data usually vary with the environ-
ment to which the alloys are exposed. In 33% HNO3, for example, the critical
chromium concentration for passivity of Cr–Fe alloys decreases to 7% Cr,
whereas in FeSO4 solution it increases to 20% Cr; only in aqueous solutions of
about pH 7 is the critical composition equal to 12%. This effect of environment
is to be expected because whether an alloy becomes passive depends on whether
the corrosion rate equals or exceeds the specific icritical for passivity in the given
environment. As seen in Fig. 6.11, increasing chromium content reduces icritical;
on the other hand, decreasing pH and increasing temperature increase icritical. The
corrosion rate, in turn, depends on factors of metal and environment affecting
the rate of both cathodic and anodic reactions.
It can be shown from first principles [39] that icritical = K(H+)λ where K and λ
are constants, the values of which depend on the anion. The cathodic reaction
rate in an aerated solution when controlled by oxygen reduction, on the other
hand, is given by the diffusion current idiff corresponding to the reaction 21 O2 +
H2O → 2OH− − 2e−. For an unstirred air-saturated solution, it can be shown that
idiff = 0.039 mA/cm2 (0.39 A/m2). Hence, a critical pH exists for each alloy com-
position at which icritical = idiff and above which, but not below, passivity is stable.
The observed critical pH values, for example, of 18% Cr, 8% Ni, and of 12% Cr
stainless steels in 0.1M Na2SO4 [40] are 1.4 and 5.0, respectively, in close agree-
ment with the calculated values. With iron, for which icritical is much higher than
for the stainless steels, the critical pH is approximately 10.
The structure of the passive film on alloys, as with passive films in general,
has been described both by the oxide-film theory and by the adsorption theory.
It has been suggested that protective oxide films form above the critical alloy
composition for passivity, but nonprotective oxide films form below the critical
composition. The preferential oxidation of passive constituents (e.g., chromium)
may form protective oxides (e.g., Cr2O3) above a specific alloy content, but not
below. No quantitative predictions have been offered based on this point of view,
and the fact that the passive film on stainless steels can be reduced cathodically,
but not stoichiometric Cr2O3 itself, remains unexplained.
By the adsorption theory, it is considered that, in the presence of water,
oxygen chemisorbs on chromium–iron alloys above the critical composition cor-
responding to passivity, but immediately reacts below the critical composition to
form a less protective or nonprotective oxide film. Whether the alloy favors a
chemisorbed or reaction-product film depends on the electron configuration of
the alloy surface, in particular on d-electron interaction. The electron configura-
tion theory describes the specific alloying proportions corresponding to a favor-
able d-electron configuration accompanying chemisorption and passivity. It
suggests the nature of electron interaction that determines which alloyed com-
ponent dominates in conferring its chemical properties on those of the alloy—for
example, why the properties of nickel dominate above those of copper in the
nickel–copper alloys at >30–40% Ni.
6.8.1 Nickel–Copper Alloys

Nickel, containing 0.6 d-electron vacancy per atom (as measured magnetically),
when alloyed with copper, a nontransition metal containing no d-electron vacan-
cies, confers passivity on the alloy above approximately 30–40 at.% Ni. Initiation
of passivity beginning at this composition is indicated by corrosion rates in
sodium chloride solution (Figs. 6.12 and 6.13), by corrosion pitting behavior in
seawater (Fig. 6.13), and, more quantitatively, by measured values of icritical and
ipassive (Fig. 6.14), [41–43] or by decay (Flade) potentials (Fig. 6.15) [44] in 1N
H2SO4.
Corrosion pitting in seawater is observed largely above 40% Ni because pit
growth is favored by passive–active cells (see Section 6.5), and such cells can
operate only when the alloy is passive—that is, in the range of high nickel com-
positions. Practically, this distinction is observed in the specification of materials
for seawater condenser tubes in which pitting attack must be rigorously avoided.
The cupro nickel alloys are used (10–30% Ni), but not Monel (70% Ni–Cu).
Similarly, marine fouling organisms are much less successful in establishing
themselves on the surface of nonpassive nickel–copper compositions because the
Figure 6.12. Corrosion rates of copper–nickel alloys in aerated 3% NaCl, 80°C, 48-h tests
(M.I.T. Corrosion Lab.).
104 PASSIVIT Y
Figure 6.13. Behavior of copper–nickel alloys in seawater [F. LaQue, J. Am. Soc. Nav. Eng.
53, 29 (1941)].
Figure 6.14. Values of critical and passive current densities obtained from potentiostatic
anodic polarization curves for copper–nickel alloys in 1N H2SO4, 25°C [42]. (Reproduced with
permission. Copyright 1961, The Electrochemical Society.)
Figure 6.15. Potential decay curves for nickel–copper and nickel–copper–zinc alloys in 1N
H2SO4, 25°C (two time scales). Pure copper behaves like Alloy D [36].
latter corrode uniformly at rates that release enough Cu2+ to poison fouling
organisms.* But on passive nickel–copper compositions, for which the overall
corrosion rate is much less, fouling organisms in general can gain a foothold and
flourish (Fig. 6.13).
Potentiostatic anodic polarization behavior of nickel–copper alloys in 1N
H2SO4 (Fig. 6.14) establishes that the passive current density largely disappears
above 60% Cu and vanishes completely at about 70% Cu. Polarization curves of
alloys containing >70% Cu or <30% Ni resemble those of pure copper; hence,
such alloys are not passive. Potential decay curves (Fig. 6.15) confirm that a
passive film is formed on anodically passivated alloys containing >40% Ni, but
not otherwise. In other words, alloys containing copper above the critical com-
position lose their transition-metal characteristics; that is, they no longer contain
d-electron vacancies. In this connection, the magnetic saturation moment, which
is also a function of d-electron vacancies in the alloy, becomes zero at >60% Cu.
This observation is interpreted as a filling of vacancies in the d band of electron
energy levels of nickel by electrons donated by copper. Physicists [45] have made
the assumption that, if copper and nickel atoms are considered to be alike, except
that copper contains one more electron per atom than nickel, then the 0.6 d-
electron vacancy per nickel atom is expected, as observed, to be just filled by
electrons from copper at 60 at.% Cu.
*The minimum concentration of Cu2+ required to poison marine organisms corresponds to a corro-
sion rate for copper of about 0.001 ipy or 0.5 gmd [F. LaQue and W. Clapp, Trans. Electrochem. Soc.
87, 103 (1945)].
106 PASSIVIT Y
One can also start with the alternative assumption that the two atoms main-
tain their individuality and that the vacancies per atom of nickel are a function
of alloy concentration [46]. In the gaseous state, nickel has the configuration of
3d84s2, corresponding to two d-electron vacancies or to the equivalent of two
uncoupled d-electrons in the third shell of the atom. The maximum number of
d-electrons that can be accommodated is 10, corresponding to copper: 3d104s. In
the process of condensing to a solid and forming the metallic bond, the uncoupled
electrons of any single nickel atom tend to couple with uncoupled electrons of
neighboring atoms. This results in a smaller number of electron vacancies in the
solid compared to the gas, accounting for the measured 0.6 vacancy or 0.6
uncoupled electron per nickel atom. If we assume that the intercoupling of d-
electrons increases with proximity of nickel atoms in the alloy and is a linear
function of nickel concentration, then the vacancies per nickel atom can be set
equal to 2 − (2 − 0.6) at.% Ni/100, corresponding to two vacancies for 0% Ni and
0.6 vacancy for 100% Ni. The alloy loses its transition-metal characteristics
beginning at the composition for which the total number of d-vacancies equals
the total number of donor electrons (one per copper atom), or at.% Ni (2 −
0.014 at.% Ni) = 1× at.% Cu. Setting at.% Cu = (100 − at.% Ni) and solving, the
critical composition is found to be 41 at.% Ni. This value corresponds closely to
the observed value derived from magnetic saturation data.
This model was checked by alloying small amounts of other nontransition
elements Y, or transition elements Z, with nickel–copper alloys and noting the
specific compositions at which icritical and ipassive merged or at which Flade poten-
tials disappeared. Non-transition-metal additions of valence >1 should shift the
critical composition for passivity to higher percentages of nickel, whereas
transition-metal additions should have the opposite effect. For example, one zinc
atom of valence 2 or one aluminum atom of valence 3 should be equivalent in
the solid solution alloy to two or three copper atoms, respectively. This has been
confirmed experimentally [47]. The relevant equations become
at.% Ni (2 − 0.014 at.% Ni) = 1 × at.% Cu + n at.% Y
and
at.% Ni (2 − 0.014 at.% Ni) + v at.% Z = 1 × at.% Cu
where n is the number of electrons donated per atom of Y and v is the number
of vacancies introduced per atom of Z.
By plotting 1× at.% Cu− at.% Ni (2 − 0.014 at.% Ni) with n at.% Y, a straight
line is predicted of unit negative slope for nontransition-element additions. If
plotted instead with v at.% Z for transition-metal additions, a unit positive slope
should result. A plot for the alloying additions so far studied is shown by data
summarized in Fig. 6.16 [46]. In order for the line to pass through the origin with
unit slope, it was necessary to assume approximately 80% instead of 100% dona-
tion of valence electrons. This means that valence electrons from copper and
Figure 6.16. Plot of excess electrons or d-electron vacancies in nickel–copper alloys at their
critical compositions versus electron vacancies, or electrons donated by alloying additions,
unit slope.
from other nontransition elements are presumably donated in major part to

nickel, but not entirely. Assuming 0.8 electron donor per copper atom in binary
nickel–copper alloys, the critical nickel composition below which the d-band is
filled becomes 35 at.% instead of 41 at.% as calculated earlier.* This value is
consistent with the composition at which ipassive and icritical intersect in Fig. 6.14.
Values of n for germanium, aluminum, and zinc shown in Fig. 6.16 are 4, 3,
and 2, respectively, in accord with their normal valence. For gallium, a valence
of 2 is in better accord with the other data, reflecting perhaps the known tendency
of gallium to form chemical compounds having a valence lower than 3, but other
explanations are also possible. For iron and cobalt, the number of vacancies per
atom is equated to vg − (vg − vs) at.% Z/100, where vg and vs are d-electron vacan-
cies per atom in the gas and solid, respectively. Values of vg for iron and cobalt
are 4 and 3, and for vs they are 2.2 and 1.7, respectively.
There are no observed phase changes or major discontinuities in the thermo-
dynamic properties of nickel–copper alloys at 60–70% Cu, whereas chemisorp-
tion on any metal is known to be favored by an unfilled d-band configuration
[48]. The good agreement, therefore, between observed and predicted critical
*The calculated number of d vacancies per Ni atom at this composition equals 2 − 0.014 × 35 = 1.51,
which is close to the value 1.6 assumed earlier [33, 39].
108 PASSIVIT Y
alloy compositions supports not only an effect of electron configuration on pas-

sivity, but also an adsorbed structure of the passive film.
6.8.2 Other Alloys

Because present-day theory of the metallic state does not treat the situation, the
electron configuration of alloys made up of two or more transition metals with
relation to their passive behavior is not as well understood as for the copper–
nickel system. Nevertheless, useful simplifying assumptions can be made. For
example, the most passive component of an alloy is assumed to be the acceptor
element, which tends to share electrons donated by the less passive
components.
Accordingly, for stainless steels, the d-electron vacancies of chromium are
assumed to fill with electrons from alloyed iron [41]. At the critical composition
at which vacancies of Cr are apparently filled, which occurs for alloys containing
less than 12% Cr, the corrosion behavior of the alloy is like that of iron. Above
12% Cr, the d-electron vacancies of chromium are unfilled, and the alloy behaves
more like chromium.
The critical compositions for passivity in the Cr–Ni and Cr–Co alloys, equal
to 14% Cr and 8% Cr, respectively, can also be related to the contribution of
electrons from nickel or cobalt to the unfilled d-band of chromium [49]. In the
ternary Cr–Ni–Fe solid solution system, electrons are donated to chromium
mostly by nickel above 50% Ni, but by iron at lower nickel compositions [50].
Similarly, molybdenum alloys retain in large part the useful corrosion resistance
of molybdenum (e.g., to chlorides) so long as the d-band of energy levels for
molybdenum remains unfilled. In Type 316 stainless steel (18% Cr, 10% Ni, 2–
3% Mo), for example, the weight ratio of Mo/Ni is best maintained at or above
15/85, corresponding to the observed critical ratio for passivity in the binary
molybdenum–nickel alloys equal to 15 wt.% Mo [51]. At this ratio or above,
passive properties imparted by molybdenum appear to be optimum.
6.9 EFFECT OF CATHODIC POLARIZATION AND CATALYSIS
When chromium, stainless steels, and passive iron are cathodically polarized,
passivity is destroyed. This occurs by reduction of the passive oxide or adsorbed
oxygen film, according to whichever viewpoint of passivity is adopted. In addi-
tion, according to the adsorption theory, hydrogen ions discharged on transition
metals tend to enter the metal as hydrogen atoms. Hydrogen so dissolved is
partly dissociated into protons and electrons, the latter being available to fill
vacancies in the d-band of the metal. A transition metal containing sufficient
hydrogen, therefore, is no longer able to chemisorb oxygen or become passive,
because the d-band is filled.
Often, catalytic properties also depend on ability of a metal or alloy to che-
misorb certain components of its environment. It is not surprising, therefore, that
REFERENCES 109
Figure 6.17. Catalytic efficiency of nickel–copper alloys for 2H→H2 as a function of alloy
composition (efficiency increases with values of γH) [53]. (Reproduced with permission of The
Royal Society of Chemistry.)
transition metals are typically good catalysts and that the principles of electron
configuration in alloys favoring catalytic activity are similar to those favoring
passivity. For example, when palladium, which contains 0.6 d-electron vacancy
per atom in the metallic state, is charged with hydrogen cathodically, it loses its
efficiency as a catalyst for the ortho–para hydrogen conversion [52]. This behav-
ior is explained by filling of the d-band by electrons of dissolved hydrogen, as a
result of which the metal no longer chemisorbs hydrogen. Correspondingly, the
catalytic efficiencies of palladium–gold alloys resemble palladium until the criti-
cal concentration of 60 at.% Au is reached, at which composition and above the
alloys become poor catalysts. Gold, a non-transition metal, supplies electrons to
the unfilled d-band of palladium, and magnetic measurements confirm that the
d-band is just filled at the critical gold concentration.
The catalytic effect of copper–nickel alloys as a function of composition for
the reaction 2H → H2 is shown in Fig. 6.17 [53]. Above 60 at.% Cu, the filled d-
band is less favorable to hydrogen adsorption; hence, favorable collisions of
gaseous H with adsorbed H are less probable, and the reaction rate decreases.
The similarity to passive behavior of copper–nickel alloys, which also decreases
above 60 at.% Cu, can be noted. The parallel conditions affecting passivity and
catalytic activity support the viewpoint that the passive films on transition metals
and their alloys are chemisorbed.
REFERENCES
1. H. Uhlig, History of passivity, experiments and theories, Passivity of Metals, Proceed-

ings, 4th Symposium on Passivity, R. Frankenthal and J. Kruger, editors, Electro-
chemical Society, Princeton, NJ, 1978, p. 1.
110 PASSIVIT Y
2. C. Schönbein, Pogg. Ann. 37, 390 (1836).

3. M. Faraday, Experimental Researches in Electricity, Vol. II, Dover, New York,
reprinted 1965.
4. C. Wagner, Corros. Sci. 5, 751 (1965).
5. K. Bonhoeffer, Z. Metallk. 44, 77 (1953).
6. F. Flade, Z. Physik. Chem. 76, 513 (1911).
7. U. F. Franck, Z. Naturforschung. 4A, 378 (1949).
8. P. King and H. Uhlig, J. Phys. Chem. 63, 2026 (1959)
9. H. Rocha and G. Lennartz, Arch. Eisenhüttenw. 26, 117 (1955).
10. G. Cartledge and R. Simpson, J. Phys. Chem. 61, 973 (1957).
11. H. Uhlig and P. King, J. Electrochem. Soc. 106, 1 (1959).
12. R. M. Burns, J. Appl. Phys. 8, 398 (1937).
13. H. Gatos and H. Uhlig, J. Electrochem. Soc. 99, 250 (1952).
14. H. Uhlig and T. O’Connor, J. Electrochem. Soc. 102, 562 (1955).
15. N. Tomashov, Corrosion 14, 229t (1958).
16. M. Stern and H. Wissenberg, J. Electrochem. Soc. 106, 759 (1959).
17. R. Frankenthal, J. Electrochem. Soc. 114, 542 (1967).
18. R. W. Revie, B. G. Baker, and J. O’M. Bockris, J. Electrochem. Soc. 122, 1460 (1975);
R. W. Revie, J. O’M. Bockris, and B. G. Baker, Surface Science 52, 664 (1975).
19. M. J. Graham, Corrosion 59(6), 475 (2003).
20. H. Uhlig, Corros. Sci. 7, 325 (1967).
21. H. H. Uhlig, Z. Elektrochem. 62, 626 (1958).
22. H. Uhlig and S. Lord, J. Electrochem. Soc. 100, 216 (1953).
23. A. MacRae, Surface Sci. 1, 319 (1964).
24. G. Okamoto and T. Shibata, Nature 206, 1350 (1965).
25. H. Leckie and H. Uhlig, J. Electrochem. Soc. 113, 1262 (1966).
26. H. Uhlig and J. Gilman, Corrosion 20, 289t (1964).
27. H. Leckie, J. Electrochem. Soc. 117, 1152 (1970).
28. M. A. Streicher, Austenitic and Ferritic Stainless Steels, in Uhlig’s Corrosion Hand-
book, 2nd edition, R. W. Revie, editor, Wiley, New York, 2000, p. 620; Mater. Perform.
36, 65 (1997).
29. H. Kaesche, Z. Physik. Chem. N. F. (F.R.D.) 34, 87 (1962); H. Böhni and H. Uhlig, J.
Electrochem. Soc. 116, 906 (1969).
30. J. Horvath and H. Uhlig, J. Electrochem. Soc. 115, 791 (1968).
31. Y. Kolotyrkin, Corrosion 19, 261t (1963).
32. N. Greene, C. Bishop, and M. Stern, J. Electrochem. Soc. 108, 836 (1961).
33. C. Hall, Jr., and N. Hackerman, J. Phys. Chem. 57, 262 (1953); F. Poser and E. Bohlmann,
Second Symposium on Fresh Water from the Sea, Athens, Greece, May, 1967.
34. T. Hoar, D. Mears, and G. Rothwell, Corros. Sci. 5, 279 (1965).
35. H. Böhni, Localized Corrosion of Passive Metals, in Uhlig’s Corrosion Handbook, 2nd
edition, R. W. Revie, editor, Wiley, New York, 2000, pp. 175–176.
36. G. Tammann, Z. Anorg. Allgem. Chem. 169, 151 (1928); (with E. Sotter), ibid. 127, 257
(1923).
GENER AL REFERENCES 111
37. H. Uhlig, Trans. Electrochem. Soc. 85, 307 (1944).

38. H. Feller and H. Uhlig, J. Electrochem. Soc. 107, 864 (1960).
39. H. H. Uhlig, J. Electrochem. Soc. 108, 327 (1961).
40. H. Leckie, Corrosion 24, 70 (1968).
41. H. Uhlig, Z. Elektrochem. 62, 700 (1958).
42. J. Osterwald and H. Uhlig, J. Electrochem. Soc. 108, 515 (1961).
43. F. Mansfeld and H. Uhlig, J. Electrochem. Soc. 117, 427 (1970).
44. F. Mansfeld and H. Uhlig, Corros. Sci. 9, 377 (1969).
45. C. Kittel, Introduction to Solid State Physics 3rd edition, Wiley, New York, 1968,
p. 581.
46. H. H. Uhlig, Electrochim. Acta 16, 1939 (1971).
47. F. Mansfeld and H. Uhlig, J. Electrochem. Soc. 115, 900 (1968).
48. D. Hayward and B. Trapnell, Chemisorption, Butterworths, Washington, D.C., 1964,
p. 8.
49. A. Bond and H. Uhlig, J. Electrochem. Soc. 107, 488 (1960).
50. H. Feller and H. Uhlig, J. Electrochem. Soc. 107, 864 (1960).
51. H. Uhlig, P. Bond, and H. Feller, J. Electrochem. Soc. 110, 650 (1963).
52. A. Couper and D. Eley, Discussions Faraday Soc. 8, 172 (1950).
53. W. Hardy and J. Linnett, Trans. Faraday Soc. 66, 447 (1970).
GENERAL REFERENCES
H. Böhni, Localized corrosion of passive metals, in Uhlig’s Corrosion Handbook, 2nd

G. S. Frankel, Pitting corrosion, in ASM Handbook, Vol. 13A, Corrosion: Fundamentals,
Testing, and Protection, ASM International, Materials Park, OH, 2003, pp. 236–241.
J. Kruger, Passivity, in Uhlig’s Corrosion Handbook, 2nd edition, R. W. Revie, editor,
J. Kruger, Passivity, in ASM Handbook, Vol. 13A, Corrosion: Fundamentals, Testing, and
Protection, ASM International, Materials Park, OH, 2003, pp. 61–67.
Passivation of Metals and Semiconductors, and Properties Of Thin Oxide Layers, A Selec-
tion of Papers from the 9th International Symposium, Paris, France, 27 June–1 July
2005, P. Marcus and V. Maurice, editors, Elsevier, Amsterdam, 2006.
Passivity and Localized Corrosion, An International Symposium in Honor of Professor
Norio Sato, M. Seo, B. MacDougall, H. Takahashi, and R. G. Kelly, editors, Electro-
chemical Society, Pennington, NJ, 1999.
Passivity of Metals and Semiconductors, Proceedings of the Eighth International Sympo-
sium, May 9–15, 1999, Jasper, Alberta, Canada, M. B. Ives, J. L. Luo, and J. R. Rodda,
editors, Electrochemical Society, Pennington, NJ, 2001.
Proceedings of the Symposium on Passivity and Its Breakdown, P. M. Natishan, H. S.
Isaacs, M. Janik-Czachor, V. A. Macagno, P. Marcus, and M. Seo, editors, Electro-
chemical Society, Pennington, NJ, 1997.
112 PASSIVIT Y
PROBLEMS
1. Calculate the minimum concentration of oxygen in milliliters per liter neces-

sary to passivate iron in 3% Na2SO4; also for 12% Cr–Fe alloy. (D for O2 at
25°C = 2 × 10−5 cm2/s) (Hint: Equate limiting diffusion current for reduction
of oxygen to critical current density for passivity.)
2. Calculate the standard Flade potential at 25°C for iron, assuming that the
passive-film substance represented schematically as O·M in Eq. (6.2) in
Section 6.2 is (a) Fe2O3, (b) Fe3O4, and (c) chemisorbed oxygen. (Data: ΔG°
of formation for Fe2O3 = −741.0 kJ/mole Fe2O3; for Fe3O4, ΔG° = −1014 kJ/
mole Fe3O4; for H2O (l), ΔG° = −237.2 kJ/mole H2O; and for H+, ΔG° = 0.
For chemisorption of oxygen on Fe, ΔH° = −314 kJ/mole O2; ΔS° = −193 J/
mole O2-°C (estimated from ΔS° value for chemisorbed N2.).
3. Calculate the absolute emf of the cell:
stainless steel; O 2(0.2atm), 0.001M ZnSO4(pH = 3.0); Zn
assuming that passive stainless steel acts as a reversible oxygen electrode.

What is the change of emf per 1 atm O2 pressure?
4. From the standard Flade potential for iron, calculate the apparent free energy
of formation of the passive film per gram-atom of oxygen. Do the same for
nickel and chromium.
5. A pit in 18–8 stainless steel exposed to seawater grows to a depth of 6.5 cm in

one year. To what average current density at the base of the pit does this rate
correspond?
6. The steady-state passive current density for iron in 1N H2SO4 is 7 μA/cm2.

How many atom layers of iron are removed from a smooth electrode surface
every minute?
7. Derive the relation log(Cl−) = k log(anion) + const, where (anion) is the

minimum activity of anion necessary to inhibit pitting of a passive metal in a
chloride solution of activity (Cl−). Assume that the amount of ion a adsorbed
per unit area follows the Freundlich adsorption isotherm, a = k1(anion)1/n1,
where k1 and n1 are constants, and that at a critical ratio of adsorbed Cl−
to adsorbed anion the passive film is displaced by Cl−, allowing a pit to
initiate.
PROBLEMS 113
Answers to Problems
1. 31,800; 0.32 mL/liter.
2. (a) −0.051 V; (b) −0.085 V; (c) 0.57 V.
3. 1.90 V; 0.032 V/atm at 0.2 atm O2 pressure.
4. For iron, −115 kJ/g-atom O.
5. 6 × 10−3 A/cm2.
6. 0.5.
7
IRON AND STEEL
7.1 INTRODUCTION
The electrochemical theory of corrosion, as described earlier, relates corrosion

to a network of short-circuited galvanic cells on the metal surface. Metal ions go
into solution at anodic areas in an amount chemically equivalent to the reaction
at cathodic areas. At anodic areas, the following reaction takes place:
Fe → Fe2+ + 2e − (7.1)
This reaction is rapid in most media, as shown by lack of pronounced polarization

when iron is made anode employing an external current. When iron corrodes,
the rate is usually controlled by the cathodic reaction, which, in general, is much
slower (cathodic control). In deaerated solutions, the cathodic reaction is
1
H+ → H2 − e− (7.2)
2
This reaction proceeds rapidly in acids; as pH is reduced, the equilibrium poten-
tial of the hydrogen electrode becomes more noble; hence, φC − φA becomes
larger, and the resulting corrosion current increases. On the other hand, this
reaction proceeds slowly in alkaline or neutral aqueous media. The corrosion
115
116 IRON AND STEEL
rate of iron in deaerated water at room temperature, for example, is less than
0.005 mm/y (0.1 gmd). The rate of hydrogen evolution at a specific pH depends
on the presence or absence of low hydrogen overpotential impurities in the metal.
For pure iron, the metal surface itself provides sites for H2 evolution; hence, high-
purity iron continues to corrode in acids, but at a measurably lower rate than
does commercial iron.
The cathodic reaction can be accelerated by dissolved oxygen in accord with
the following reaction, a process called depolarization:
1
2 H + + O2 → H 2 O − 2e − (7.3)
2
Dissolved oxygen reacts with hydrogen atoms adsorbed at random on the
iron surface, independent of the presence or absence of impurities in the metal.
The oxidation reaction proceeds as rapidly as oxygen reaches the metal
surface.
Adding (7.1) and (7.3), using the reaction H2O → H+ + OH−, we obtain
1
Fe + H 2 O + O2 → Fe(OH)2 (7.4)
2
Hydrous ferrous oxide (FeO·nH2O) or ferrous hydroxide [Fe(OH)2] composes

the diffusion-barrier layer next to the iron surface through which O2 must diffuse.
The pH of saturated Fe(OH)2 is about 9.5, so that the surface of iron corroding
in aerated pure water is always alkaline. The color of Fe(OH)2, although white
when the substance is pure, is normally green to greenish black because of incipi-
ent oxidation by air. At the outer surface of the oxide film, access to dissolved
oxygen converts ferrous oxide to hydrous ferric oxide or ferric hydroxide, in
accord with
1 1
Fe(OH)2 + H 2 O + O2 → Fe(OH)3 (7.5)
2 4
Hydrous ferric oxide is orange to reddish brown in color and comprises most of
ordinary rust. It exists as nonmagnetic αFe2O3 (hematite) or as magnetic γFe2O3,
with the α form having the greater negative free energy of formation, that is,
greater stability. Saturated Fe(OH)3 is nearly neutral in pH. A magnetic hydrous
ferrous ferrite, Fe3O4·nH2O, often forms a black intermediate layer between
hydrous Fe2O3 and FeO. Hence rust films normally consist of three layers of iron
oxides in different states of oxidation.
7.2 AQUEOUS ENVIRONMENTS
7.2.1 Effect of Dissolved Oxygen

7.2.1.1 Air-Saturated Water. In neutral or near-neutral water at ambient
temperatures, dissolved oxygen is necessary for appreciable corrosion of iron. In
AQUEOUS ENVIRONMENTS 117
air-saturated water, the initial corrosion rate may reach a value of about 10 gmd.
This rate diminishes over a period of days as the iron oxide (rust) film is formed
and acts as a barrier to oxygen diffusion. The steady-state corrosion rate may be
1.0–2.5 gmd, tending to be higher the greater the relative motion of water with
respect to iron. Since the diffusion rate at steady state is proportional to oxygen
concentration, it follows from (7.3) that the corrosion rate of iron is also propor-
tional to oxygen concentration. The concentration of dissolved oxygen in air-
saturated, natural fresh waters at ordinary temperatures is 8–10 ppm. In the
absence of dissolved oxygen, the corrosion rate at room temperature is negligible
both for pure iron and for steel.
In the absence of diffusion-barrier films of corrosion products on the surface,
the theoretical corrosion current density, i (A/cm2), of steel in stagnant, air-
saturated fresh water is [cf. Eq. (5.5), Section 5.4]
i= ( DnF
δ )
c × 10 −3
(7.6)
where D is the diffusion coefficient for dissolved oxygen in water (cm2/s), δ is the
thickness of the stagnant layer of electrolyte next to the electrode surface, c is
the concentration of oxygen, and the other terms have their usual significance.
Using D = 2 × 10−5 cm2/s, n = 4 eq/mole, F = 96,500 C/eq, δ = 0.05 cm, and c = 8/32
× 10−3 mole/liter at 25 °C, we obtain i = 38.6 × 10−6 A/cm2, corresponding to a cor-
rosion rate of 0.45 mm/y [1].
7.2.1.2 Higher Partial Pressures of Oxygen. Although increase in oxygen

concentration at first accelerates corrosion of iron, it is found that, beyond a
critical concentration, the corrosion drops again to a low value [2]. In distilled
water, the critical concentration of oxygen above which corrosion decreases
again, is about 12 mL O2/liter (Fig. 7.1). This value increases with dissolved salts
and with temperature, and it decreases with an increase in velocity and pH. At
pH of about 10, the critical oxygen concentration reaches the value for air-
saturated water (6 mL O2/liter) and is still less for more alkaline solutions.
The decrease of corrosion rate is caused by passivation of iron by oxygen,
as shown by potentials of iron in air-saturated H2O of −0.4 to −0.5 V versus
S.H.E. and 0.1 to 0.4 V in oxygen-saturated H2O (28 mL O2/liter). Apparently, at
higher partial pressures, more oxygen reaches the metal surface than can be
reduced by the corrosion reaction—the excess, therefore, is available to form the
passive film; increasing the cathodic reaction rate by higher oxygen concentration
increases polarization of anodic areas until the critical current density for passiv-
ity is reached (see Fig. 6.1, Section 6.2) [3].
Because passivity accompanies higher oxygen pressures, passive–active cells
are established in the event that passivity breaks down locally (e.g., at crevices).
Such breakdown is accompanied by severe pitting, particularly at higher tem-
peratures, in the presence of halide ions, or at a critical pressure of oxygen where
passivity is on the verge of either forming or breaking down. This behavior
limits the practical use of high partial oxygen pressures as a means of reducing
118 IRON AND STEEL
Figure 7.1. Effect of oxygen concentration on corrosion of mild steel in slowly moving dis-
tilled water, 48-h test, 25 °C [2]. (Reproduced with permission. Copyright 1955, The Electro-
chemical Society.)
corrosion of steel. In appreciable concentration of chlorides, as in seawater, pas-

sivity of iron is not established at all, and in such media increased oxygen pressure
results in an increased corrosion rate.
7.2.1.3 Microbiologically Influenced Corrosion. Microbiologically influ-

enced corrosion (MIC) is corrosion that is caused by the presence and activities
of microorganisms—that is, organisms that cannot be seen individually with the
unaided human eye, including microalgae, bacteria, and fungi [4]. Microbiologi-
cally influenced corrosion can cause various forms of localized corrosion, includ-
ing pitting, dealloying, enhanced erosion corrosion, enhanced galvanic corrosion,
stress corrosion cracking, and hydrogen embrittlement [4]. As a result of MIC,
corrosion can occur at locations where it would not be predicted, and it can occur
at very high rates. All engineering alloys, with the exception of titanium and high
chromium–nickel alloys, have been reported to undergo MIC. Furthermore, MIC
has been documented to take place in seawater, fresh water, distilled/demineral-
ized water, hydrocarbon fuels, process chemicals, foods, soils, human plasma,
saliva, and sewage [4].
Although sulfate-reducing bacteria (SRBs), active only in anaerobic (oxygen-
free) environments, are a very common cause of corrosion and have been exten-
sively studied, MIC can also be caused by other types of microorganisms—for
example, Thiobacilli [sulfur-oxidizing bacteria (SOB), which oxidize sulfur com-
pounds to sulfuric acid] and other acid-producing microorganisms, including both
bacteria and fungi.
Microbes can adhere to metal surfaces forming a biofilm, consisting of a

community of microorganisms, leading to corrosion [4, 5]. When the acidic prod-
ucts of bacterial action are trapped at the biofilm–metal interface, their impact
on corrosion is intensified [6].
Although iron does not corrode appreciably in deaerated water, the corro-
sion rate in some natural deaerated environments is found to be abnormally high.
These high rates have been traced to the presence of sulfate-reducing bacteria
(e.g., Desulfovibrio desulfuricans). Their relation to an observed accelerated cor-
rosion rate in soils low in dissolved oxygen was first observed by von Wolzogen
Kühr in Holland [7]. The bacteria are curved, measuring about 1 × 4 μm, and are
found in many waters and soils. They thrive only under anaerobic conditions in
the pH range of about 5.5–8.5. Certain varieties multiply in fresh waters and in
soils containing sulfates, others flourish in brackish waters and seawater, and
still others are stated to exist in deep soils at temperatures as high as 60–80 °C
(140–175 °F).
Sulfate-reducing bacteria easily reduce inorganic sulfates to sulfides in the
presence of hydrogen or organic matter, and they are aided in this process by the
presence of an iron surface. The aid that iron provides in this reduction is prob-
ably to supply hydrogen, which is normally adsorbed on the metal surface and
which the bacteria use in reducing SO4. For each equivalent of hydrogen atoms
they consume, one equivalent of Fe2+ enters solution to form rust and FeS. The
bacteria, therefore, probably act essentially as depolarizers.
A possible reaction sequence can be outlined as follows:
Anode: 4 Fe → 4 Fe2 + + 8e − (7.7)
Cathade: 8 H 2 O + 8e − → 8 Hads on Fe + 8OH − (7.8)
8 Hads + Na 2SO4 ⎯bacteria

⎯⎯⎯ → 4 H 2O + Na 2S (7.9)
Na 2S + 2H 2CO3 → 2 NaHCO3 + H 2S (7.10)
Summary: 4 Fe + 2 H 2O + Na 2SO4 + 2 H 2CO3 → 3Fe(OH)2 + FeS + 2 NaHCO3

(7.11)
Ferrous hydroxide and ferrous sulfide are formed in the proportion of 3 moles
to 1 mole. Analysis of a rust in which sulfate-reducing bacteria were active shows
this approximate ratio of oxide to sulfide. Qualitatively, the action of sulfate-
reducing bacteria as the cause of corrosion in a water initially free of sulfides can
be detected by adding a few drops of hydrochloric acid to the rust and noting
the smell of hydrogen sulfide.
120 IRON AND STEEL
In addition to the cathodic reaction listed in (7.8), other cathodic reactions

could be considered [8, 9], such as the reduction of H2S:
2 H 2S + 2e − → 2 HS− + H 2 (7.12)
Severe damage by sulfate-reducing bacteria has occurred particularly in oil-well

casing, buried pipelines, water-cooled rolling mills, and pipe from deep water
wells. Within 2 years, well water in the U.S. Midwest caused failure of a galvanized
water pipe 50 mm (2 in.) in diameter by action of sulfate-reducing bacteria,
whereas municipal water using similar wells, but which was chlorinated before-
hand, was much less corrosive.
A combination of low temperature and low humidity is one approach to
controlling the growth of bacteria, but fungi may be capable of growing under
such conditions [10]. Regular cleaning is a good practice to prevent biofilm for-
mation and subsequent corrosion. Chlorination is used to eliminate bacteria that
cause corrosion, but this treatment can produce byproducts that are environmen-
tally unacceptable [10]. Aeration of water reduces activity of anaerobic bacteria
since they are unable to thrive in the presence of dissolved O2. Addition of
certain biocides can be beneficial, but microorganisms are capable of becoming
resistant to specific chemicals after long-term use. Eradication of microbial popu-
lations may be achieved by combining several chemicals or by increasing the
concentration of a biocide [10].
7.2.2 Effect of Temperature

When corrosion is controlled by diffusion of oxygen, the corrosion rate at a given
oxygen concentration approximately doubles for every 30 °C (55 °F) rise in tem-
perature [11]. In an open vessel, allowing dissolved oxygen to escape, the rate
increases with temperature to about 80 °C (175 °F) and then falls to a very low
value at the boiling point (Fig. 7.2). The lower corrosion rate above 80 °C is
related to a marked decrease of oxygen solubility in water as the temperature is
raised, and this effect eventually overshadows the accelerating effect of tempera-
ture alone. In a closed system, on the other hand, oxygen cannot escape, and the
corrosion rate continues to increase with temperature until all the oxygen is
consumed.
When corrosion is attended by hydrogen evolution, the rate increase is more
than double for every 30 °C rise in temperature. The rate for iron corroding in
hydrochloric acid, for example, approximately doubles for every 10 °C rise in
temperature.
7.2.3 Effect of pH
The effect of pH of an aerated pure, or soft, water on corrosion of iron at room
temperature is shown in Fig. 7.3 [12]; however, the effect of pH may be different
in a hard water, in which a protective film of CaCO3 forms on the metal surface,
Figure 7.2. Effect of temperature on corrosion of iron in water containing dissolved oxygen.
(Reprinted with permission from F. N. Speller, Corrosion, Causes and Prevention, 3rd edition,
McGraw-Hill, New York, 1951, p. 168.)
Figure 7.3. Effect of pH on corrosion of iron in aerated soft water, room temperature [12].
[Reprinted with permission from W. Whitman, R. Russell, and V. Altieri, Ind. Eng. Chem. 16,
665 (1924). Copyright 1924, American Chemical Society].
as will be discussed in Section 7.2.6.1. In obtaining the data shown in Fig. 7.3,
sodium hydroxide and hydrochloric acid were used to adjust pH in the alkaline
and acid ranges.
Within the range of about pH 4–10, the corrosion rate is independent of pH
and depends only on how rapidly oxygen diffuses to the metal surface. The major
diffusion barrier of hydrous ferrous oxide is continuously renewed by the corro-
sion process. Regardless of the observed pH of water within this range, the
122 IRON AND STEEL
surface of iron is always in contact with an alkaline solution of saturated hydrous

ferrous oxide, the observed pH of which is about 9.5.*
Within the acid region, pH < 4, the ferrous oxide film is dissolved, the surface
pH falls, and iron is more or less in direct contact with the aqueous environment.
The increased rate of reaction is then the sum of both an appreciable rate of
hydrogen evolution and oxygen depolarization.
Above pH 10, an increase in alkalinity of the environment raises the pH of
the iron surface. The corrosion rate correspondingly decreases because iron
becomes increasingly passive in the presence of alkalies and dissolved oxygen,
as explained in Section 7.2.1.2. Confirming the occurrence of passivity by Defini-
tion 1 in Section 6.1, the potential of iron changes from an active value of −0.4
to −0.5 in water of pH < 10, to a noble value of 0.1 V in 1 N NaOH, with an
accompanying decrease in the corrosion rate. If the alkalinity is markedly
increased, for example, to 16 N NaOH (43%), passivity is disrupted, and the
potential achieves the very active value of −0.9 V. The corrosion rate correspond-
ingly increases slightly to 0.003–0.1 mm/y (0.05–2.0 gmd), but that is still a rela-
tively low rate. In this region, iron corrodes with formation of soluble sodium
ferrite (NaFeO2). In the absence of dissolved oxygen, the reaction proceeds with
hydrogen evolution forming sodium hypoferrite, Na2FeO2 [14]. The fact that Fe2+
is complexed by OH− in strong alkalies to form FeO−2 with accompanying reduc-
tion in activity of Fe2+ accounts for the observed active potential of iron. Although
the rate of formation of FeO−2 in concentrated alkalies at room temperature is
low, caused by marked polarization of probably both anodic and cathodic areas,
the rate becomes excessively high at boiler temperatures.
In the region of pH 4–10, the corrosion rate depends only on the rate of dif-
fusion of oxygen to the available cathodic surface. The extent of the cathodic
surface is apparently not important. This was established in an experiment of
Whitman and Russell [15], who exposed steel specimens that were copper-plated
over three-quarters of the surface to tap water of Cambridge, Massachusetts. The
total weight loss of these specimens compared to control specimens not plated
was found to be the same. All oxygen reaching the copper surface, acting as
cathode, was reduced in accord with the reaction
1
H 2 O + O2 → 2OH − − 2e −
2
and an equivalent amount of Fe2+ was formed at the iron surface acting as anode.†
In addition, all oxygen reaching cathodic areas of the iron surface itself produced
*On the other hand, some investigators, using different natural waters and different chemicals to
control pH, have observed that the corrosion rate does change with pH in the pH range 6–9. This
behavior has been attributed to reduced buffer capacity of HCO−3 (an inhibitor) as pH increases,
causing a pH at local sites that is lower than the pH that would otherwise exist in a solution of satu-
rated hydrous ferrous oxide. The reader may wish to consult the review by Matsushima on this matter
[13].
†
This equivalence is valid in waters of low conductivity only if anode and cathode areas are in close
proximity. In seawater, anodes and cathodes may be several feet apart.
an equivalent amount of Fe2+. Thus, the total amount of iron corroding was the
same regardless of whether copper was plated over part of the specimens.
However, penetration of iron in the case of the plated specimens was four times
that of the bare specimens.
Therefore, it follows that so long as oxygen diffusion through the oxide layer
is controlling, which is the case within pH 4–10, any small variation in composi-
tion of a steel and its heat treatment, or whether it is cold worked or annealed,
has no bearing on corrosion behavior, provided that the diffusion-barrier layer
remains essentially unchanged. Oxygen concentration, temperature, and veloc-
ity of the water alone determine the reaction rate. These facts are important
because almost all natural waters fall within the pH range 4–10. This means that
whether a high- or low-carbon steel, low-alloy steel (e.g., 1–2% Ni, Mn, Mo,
etc.), wrought iron, cast iron, or cold-rolled mild steel is exposed to fresh water
or seawater, all the observed corrosion rates in a given environment are essen-
tially the same. Many laboratory and service data obtained with a variety of
irons and steels support the validity of this conclusion [16]. A few typical data
are summarized in Table 7.1. These observations answer the once vociferous
argument that wrought iron, for example, is supposedly more corrosion resistant
than steel.
In the acid range, pH < 4, oxygen is not controlling, and the corrosion reac-
tion is established, in part, by the rate of hydrogen evolution. The latter, in turn,
depends on the hydrogen overpotential of various impurities or phases present
in specific steels or irons. The rate becomes sufficiently high in this pH range to
make anodic polarization a possible contributing factor (i.e., mixed control).
Because cementite, Fe3C, is a phase of low hydrogen overpotential, a low-carbon
steel corrodes in acids at a lower rate than does a high-carbon steel. Similarly,
heat treatment affecting the presence and size of cementite particles can appre-
ciably alter the corrosion rate. Furthermore, cold-rolled steel corrodes more
rapidly in acids than does an annealed or stress-relieved steel because cold
working produces finely dispersed low-overpotential areas originating largely
from interstitial nitrogen and carbon.
Since iron is not commonly used in strongly acid environments, the factors
governing its corrosion in media of low pH are less important than those in
natural waters and soils. Nevertheless, there are certain applications where such
factors must be considered—for example, in steam-return lines containing car-
bonic acid, as well as in food cans where fruit and vegetable acids corrode the
container with accompanying hydrogen evolution.
Less is known about the effect of impurities and metallurgical factors on
the corrosion rate in the very alkaline region (pH ∼14) where corrosion is again
accompanied by hydrogen evolution. In the passive region (pH ∼10–13), the
effect on passivity by impurities in their usual concentrations, as well as the
effect of metallurgical factors, is not expected to be pronounced. In general,
any condition producing a large cathode-to-anode area ratio facilitates achieve-
ment of passivity and increases the stability of the passive state once it is
achieved.
124 IRON AND STEEL
TABLE 7.1. Corrosion Rates of Various Steels when Oxygen Diffusion Is Controlling
% Carbon Treatment Environment Temperature Corrosion Rate
of Test
ipy mm/y
Effect of Heat Treatment

0.39 Cold drawn, Distilled 65 °C 0.0036 0.091
annealed 500 °C water
0.39 Normalized Distilled 65 °C 0.0034 0.086
20 min at 900 °C water
0.39 Quenched Distilled 65 °C 0.0033 0.084
850 °C, various water
specimens
tempered at
300–800 °C
Effect of Carbon
0.05 Not stated 3% NaCl Room 0.0014 0.036
Effect of Alloying
0.13 Not stated Seawater 0.004 0.10
0.10, 0.34% Not stated Seawater 0.005 0.13
Cu
0.06, 2.2% Not stated Seawater 0.005 0.13
Ni
Wrought Not stated Seawater 0.005 0.13
iron
Source: F. N. Speller, Corrosion, Causes and Prevention, McGraw-Hill, New York, 1951.
7.2.3.1 Corrosion of Iron in Acids. We have seen that, in strong acids, such
as hydrochoric and sulfuric acids, the diffusion-barrier oxide film on the surface
of iron is dissolved below pH 4. In weaker acids, such as acetic or carbonic acids,
dissolution of the oxide occurs at a higher pH; hence, the corrosion rate of iron
increases accompanied by hydrogen evolution at pH 5 or 6. This difference is
explained [12] by the higher total acidity or neutralizing capacity of a partially
dissociated acid compared with a totally dissociated acid at a given pH. In other
words, at a given pH, there is more available H+ to react with and dissolve the
barrier oxide film using a weak acid compared to a strong acid.
The increased corrosion rate of iron as pH decreases is not caused by
increased hydrogen evolution alone; in fact, greater accessibility of oxygen to the
metal surface on dissolution of the surface oxide favors oxygen depolarization,
which is often the more important reason. The sensitivity of the corrosion rate
of iron or steel in nonoxidizng acids to dissolved oxygen concentration is shown
TABLE 7.2. Effect of Dissolved Oxygen on Corrosion of Mild Steel in Acids [17]
Acid Corrosion Rate (mm/y) Ratio
Under O2 Under H2
6% acetic 13.9 0.16 87

6% H2SO4 9.1 0.79 12
4% HCl 12.2 0.79 15
0.04% HCl 9.9 0.14 71
1.2% HNO3 46 40 1.2
by data of Table 7.2. In 6% acetic acid at room temperature, the ratio of corro-
sion rate with oxygen present to corrosion rate with oxygen absent is 87. In oxi-
dizing acids, such as nitric acid, which act as depolarizers and for which the
corrosion rate is, therefore, independent of dissolved oxygen, the ratio is almost
unity. In general, the ratios are larger the more dilute the acid. In more concen-
trated acids, the rate of hydrogen evolution is so pronounced that oxygen has
difficulty in reaching the metal surface. Hence, depolarization in more concen-
trated acids contributes less to the overall corrosion rate than in dilute acids, in
which diffusion of oxygen is impeded to a lesser extent.
Traces of oxygen in dilute H2SO4—or substantial amounts in more concen-
trated acid, in which the corrosion rate is higher—inhibit the corrosion reaction.
For zone-refined iron, the average corrosion rate in aerated 1.0 N H2SO4 at 25 °C
was found to be 41.5 gmd, whereas in hydrogen-saturated acid the rate was
68.0 gmd [18]. Similar effects are shown by pure 9.2% Co–Fe alloy in 1.0 N H2SO4,
both aerated and deaerated, for which the corrosion rates are high and the diffu-
sion of oxygen is impeded by rapid hydrogen evolution (Fig. 7.4) [18]. Potential
and polarization measurements indicate that oxygen in small concentrations at
the metal surface increases cathodic polarization, thereby decreasing corrosion;
in higher concentrations, oxygen acts mainly as a depolarizer, increasing the rate.
The important depolarizing action of dissolved oxygen suggests that the
velocity of an acid should markedly affect the corrosion rate. This effect is
observed, particularly with dilute acids, for reasons previously stated (Fig. 7.5).
In addition, the inhibiting effect of dissolved oxygen is observed within a critical
velocity range, with the critical velocity becoming higher the more rapid the
inherent reaction rate of steel with the acid. Relative motion of acid with respect
to metal sweeps away hydrogen bubbles and reduces the thickness of the stagnant
liquid layer at the metal surface, allowing more oxygen to reach the metal
surface. Accordingly, the corrosion rate of steel in the presence of air in 0.0043 N
H2SO4 at a velocity of 3.7 m/s (12 ft/s) is the same as that in 5 N acid at the same
velocity. At rest, the ratio of corrosion rates is about 12 [19]. In the absence of
dissolved oxygen, only hydrogen evolution occurs at cathodic areas, and an effect
of velocity is no longer observed (Fig. 7.5) [20]. This result is expected because
hydrogen overpotential (activation polarization) is insensitive to velocity of the
electrolyte.
126 IRON AND STEEL
Figure 7.4. Corrosion of 9.2% Co–Fe alloy in 1 N H2SO4, showing an inhibiting effect of dis-
solved oxygen, 25 °C [18].
Figure 7.5. Effect of velocity on corrosion of mild steel (0.12% C) in 0.33 N sulfuric acid under
air and oxygen [19], 23 ± 2 °C, 45-min test, rotating spec., 18 mm diameter, 56 mm long; and
0.009% C steel under nitrogen [20].
For aerated acid, the minimum rate occurs at higher velocities the more
concentrated the acid because the rate of hydrogen evolution is more pronounced,
thereby impeding oxygen diffusion to the metal surface. Similarly, the minimum
shifts to higher velocities the higher the carbon content of the steel because the
corrosion rate and the accompanying hydrogen evolution both increase with
carbon content.
7.2.4 Effect of Galvanic Coupling

The classic experiment of Whitman and Russell, which showed that weight loss
of iron coupled to copper is the same as if the entire surface had been iron, also
showed that the actual penetration of iron increases when iron is coupled to a
more noble metal. This experiment, therefore, provides information about the
effect of coupling on the corrosion rate of the less noble component of a couple.
For the situation where diffusion of a depolarizer is controlling, the general rela-
tion between penetration, p (proportional to corrosion rate), of a metal having
area Aa coupled to a more noble metal of area Ac, is given by
(
p = p0 1 +
Ac
Aa ) (7.13)
where p0 is the normal penetration of the uncoupled metal.

If the ratio of areas Ac/Aa is large, the increased corrosion caused by coupling
can be considerable. Conductivity of the electrolyte and geometry of the system
enter the problem because only that part of the cathode area is effective for
which resistance between anode and cathode is not a controlling factor. In soft
tap water, the critical distance between copper and iron may be 5 mm; in seawa-
ter, it may be several decimeters. The critical distance is greater the larger the
potential difference between anode and cathode. All more noble metals acceler-
ate corrosion similarly, except when a surface film (e.g., on lead) acts as a barrier
to diffusion of oxygen or when the metal is a poor catalyst for reduction of
oxygen.
In the case of coupled metals exposed to deaerated solution for which cor-
rosion is accompanied by hydrogen evolution, increased area of the more noble
metal also increases corrosion of the less noble metal. Figure 7.6 shows polariza-
tion curves for an anode that polarizes little in comparison to a cathode at which
hydrogen is evolved (cathodic control). Slope 1 represents polarization of a noble
metal area having high hydrogen overpotential. Slopes 2 and 3 represent metals
with lower hydrogen overpotential. The corresponding galvanic currents are
given by projecting the intersection of anode–cathode polarization curves to the
log I axis. In general, any metal on which hydrogen discharges acts as a hydrogen
electrode with an equilibrium potential at 1 atm hydrogen pressure of
−0.059pH volt. When a corroding metal is coupled to a more noble metal of vari-
able area, the situation is shown in Fig. 7.7, where log current density is plotted
instead of log total current. If the anode of area Aa is coupled to the more noble
128 IRON AND STEEL
Figure 7.6. Effect of hydrogen overpotential of cathode on galvanic corrosion in deaerated

nonoxidizing acids.
Figure 7.7. Effect of anode–cathode area ratio on corrosion of galvanic couples in deaerated
nonoxidizing acids. (a) Large cathode coupled to small anode. (b) Large anode coupled to
small cathode.
metal of area Ac, then the galvanic current density at the anode produced by
coupling can be shown to be
−φ galv − 0.059 pH A
log iA,galv = + log c i0 (7.14)
β Aa
where φgalv is the corrosion potential (S.H.E.) of the galvanic couple (measured
at a large distance compared to dimensions of the couple), β and i0 are the
Tafel constant and exchange current density, respectively, for hydrogen ion
I
discharge on the noble metal, and galv = iA,galv .
Aa
7.2.5 Effect of Velocity on Corrosion in Natural Waters

In natural fresh water, the pH is usually too high for hydrogen evolution to play
an important role, and relative motion of the water at first increases the corrosion
rate by bringing more oxygen to the surface. At sufficiently high velocities,
enough oxygen may reach the surface to cause partial passivity. If this happens,
the rate decreases again after the initial increase (Fig. 7.8). Should the velocity
increase still further, the mechanical erosion of passive or corrosion-product films
again increases the rate. The maximum corrosion rate preceding passivity occurs
at a velocity that varies with smoothness of the metal surface and with impurities
in the water. In the presence of high concentration of Cl−, as in seawater, passivity
is not established at any velocity, and the corrosion rate increases without a
Figure 7.8. Effect of velocity on corrosion of mild steel tubes containing Cambridge water,
21 °C, 48-h tests [21]. [Reprinted with permission from R. Russell et al., Ind. Eng. Chem. 19, 65
(1927). Copyright 1927, American Chemical Society.]
130 IRON AND STEEL
Figure 7.9. Effect of velocity on corrosion of steel in seawater [22].
decrease at any intermediate velocity (Fig. 7.9). The same behavior is expected
at elevated temperatures that preclude the possibility of passivity by dissolved
oxygen.
7.2.5.1 Cavitation–Erosion. If conditions of velocity are such that repeti-

tive low-pressure (below atmospheric) and high-pressure areas are developed,
bubbles form and collapse at the metal–liquid interface. This phenomenon is
called cavitation. The damage to a metal caused by cavitation is called cavita-
tion–erosion, or cavitation damage. The damage can be reproduced in the labora-
tory using metal probes undergoing forced high-frequency mechanical oscillations
normal to the metal surface. The surface becomes deeply pitted and appears to
be spongy (Fig. 7.10), or like a honeycomb-like structure [24]. Damage from this
cause may be purely mechanical, as is experienced with glass or plastics or when
damage to a metal occurs in organic liquids. The damage, however, may involve
both chemical and mechanical factors, particularly if protective films are
destroyed, allowing corrosion to proceed at a higher rate. The part played by
chemical factors is apparent, for example, from increased metal loss in laboratory
tests using seawater compared to fresh water.
Cavitation–erosion occurs typically on rotors of pumps, on the trailing faces
of propellers and of water-turbine blades, and on the water-cooled side of diesel-
engine cylinders [25]. Cavitation attack is usually controlled by design and mate-
rials selection [26]. Damage can be reduced by operating rotary pumps at the
highest possible head of pressure in order to avoid bubble formation. For turbine
blades, aeration of water cushions the damage caused by collapse of bubbles.
There is a wide range of polymers with good resistance to cavitation–erosion and
excellent resistance to corrosion—for example, high-density polyethylene has a
cavitation–erosion resistance similar to that of nickel-based and titanium alloys
[26, 27]. Since 18–8 stainless steel is one of the relatively resistant alloys, it is used
as a facing for water-turbine blades. To reduce damage of diesel-engine cylinder
liners, addition of inhibitor to the cooling water has proved effective [28].
Figure 7.10. Cavitation–erosion damage to cylinder liner of a diesel engine [23]. (Copyright
NACE International, 1950.)
7.2.6 Effect of Dissolved Salts

The effect of sodium chloride concentration on corrosion of iron in air-saturated
water at room temperature is shown in Fig. 7.11. The corrosion rate first increases
with salt concentration and then decreases, with the value falling below that for
distilled water when saturation is reached (26% NaCl).
Since oxygen depolarization controls the rate throughout the sodium chlo-
ride concentration range, it is important to understand why the rate first increases,
reaching a maximum at about 3% NaCl (seawater concentration), and then
decreases. Oxygen solubility in water decreases continuously with sodium chlo-
ride concentration, explaining the lower corrosion rates at the higher sodium
chloride concentrations. The initial rise appears to be related to a change in the
protective nature of the diffusion-barrier rust film that forms on corroding iron.
In distilled water having low conductivity, anodes and cathodes must be located
132 IRON AND STEEL
Figure 7.11. Effect of sodium chloride concentration on corrosion of iron in aerated solu-
tions, room temperature (composite data of several investigations).
relatively near each other. Consequently, OH− ions forming at cathodes in accor-
dance with [cf. Eqs. (7.3) and (7.4), Sec. 7.1]
1
O2 + H 2 O → 2OH − − 2e − (7.15)
2
are always in the proximity of Fe2+ ions forming at nearby anodes, resulting in a
film of Fe(OH)2 adjacent to and adherent to the metal surface. This film provides
an effective diffusion-barrier film.
In sodium chloride solutions, on the other hand, the conductivity is greater;
hence, additional anodes and cathodes can operate much further removed one
from the other. At such cathodes, NaOH does not react immediately with FeCl2
formed at anodes; instead, these substances diffuse into the solution and react to
form Fe(OH)2 away from the metal surface. Any Fe(OH)2 so formed does not
provide a protective barrier layer on the metal surface. Hence, iron corrodes
more rapidly in dilute sodium chloride solution because more dissolved oxygen
can reach cathodic areas. Above 3% NaCl, the continuing decreased solubility
of oxygen becomes more important than any change in the diffusion-barrier
layer; hence, the corrosion rate decreases.
Alkali-metal salts (e.g., KCl, LiCl, Na2SO4, KI, NaBr, etc.) affect the corro-
sion rate of iron and steel in approximately the same manner as sodium chloride.
Chlorides appear to be slightly more corrosive in the order Li, Na, and K [29].
Alkaline-earth salts (e.g., CaCl2, SrCl2) are slightly less corrosive than alkali-
metal salts. Nitrates appear to be slightly less corrosive than chlorides or sulfates
at low concentrations (0.2–0.25 N), but not necessarily at higher concentrations
[30]. The small differences for all these solutions may arise, for example, from
their specific effect on the Fe(OH)2 diffusion-barrier layer, or perhaps from the
different adsorptive properties of the ions at a metal surface resulting in differing
anode–cathode area ratios or differing overvoltage characteristics for oxygen
reduction.
Acid salts, which are salts that hydrolyze to form acid solutions, cause cor-
rosion with combined hydrogen evolution and oxygen depolarization at a rate
paralleling that of the corresponding acids at the same pH value. Examples of

such salts are AlCl3, NiSO4, MnCl2, and FeCl2. Ammonium salts (e.g., NH4Cl)
are also acid, but produce a higher corrosion rate than corresponds to their pH
(at NH4Cl concentrations >0.05 N) [30]. Increased corrosivity is accounted for by
the ability of NH4+ to complex iron ions, thereby reducing activity of Fe2+ and
increasing the tendency of iron to corrode. Ammonium nitrate in high concentra-
tion is more corrosive (as much as eight times more) than the chloride or sulfate,
in part because of the depolarizing ability of NO−3 .
In the presence of excess NH3, common to some synthetic fertilizer solutions,
the corrosion rate in ammonium nitrate at room temperature may reach the very
high value of 50 mm/y (2 ipy). The complex formed in this case has the structure
[Fe(NH3)6](NO3)2 [31]. Since coupling mild steel to an equal area of platinum
has no effect on the rate, the reaction is apparently anodically controlled. Metal-
lurgical structure affects the rate, a cold-worked mild steel reacting much more
rapidly than one quenched from elevated temperature. This indicates that the
reaction is not diffusion-controlled, but depends instead on the rate of metal-ion
formation at the anode and perhaps also to some extent on the rate of depolar-
ization at the cathode.
Alkaline salts, which hydrolyze to form solutions of pH > 10, act as corrosion
inhibitors. They passivate iron in the presence of dissolved oxygen in the same
manner as NaOH (Fig. 7.3, Section 7.2.3). Examples of such salts are trisodium
phosphate (Na3PO4), sodium tetraborate (Na2B2O7), sodium silicate (Na2SiO3),
and sodium carbonate (Na2CO3). In addition to favoring passivation of iron by
dissolved oxygen, they may form corrosion-product layers of ferrous or ferric
phosphates in the case of Na3PO4, or analogous compounds in the case of Na2SiO3,
with such layers acting as more efficient diffusion barriers than hydrous FeO.
They may, on this account, also inhibit corrosion below pH 10 and may provide
better inhibition above pH 10 than NaOH or Na2CO3.
Oxidizing salts are either (a) good depolarizers, and therefore corrosive, or
(b) passivators and efficient inhibitors. Examples of the first class are FeCl3,
CuCl2, HgCl2, and sodium hypochlorite. They represent the most difficult class
of chemicals to handle in metal equipment. Examples of the second class are
Na2CrO4, NaNO2, KMnO4, and K2FeO4. The differences in properties accounting
for an oxidizing salt being either a depolarizer or a passivator are discussed in
Chapter 17.
7.2.6.1 Natural-Water Salts. Natural fresh waters contain dissolved

calcium and magnesium salts in varying concentrations, depending on the source
and location of the water. If the concentration of such salts is high, the water is
called hard; otherwise, it is called soft. For many years before the causes were
clearly understood, it was recognized that a soft water was more corrosive than
a hard water. For example, a galvanized-iron hot-water tank was observed to last
10–20 years before failing by pitting in Chicago Great Lakes water (34 ppm Ca2+,
157 ppm dissolved solids), whereas in Boston water (5 ppm Ca2+, 43 ppm dissolved
solids), a similar tank lasted only one to two years.
134 IRON AND STEEL
The two parameters that control corrosivity of soft waters are the pH and
the dissolved oxygen concentration. In hard waters, however, the natural deposi-
tion on the metal surface of a thin diffusion-barrier film composed largely of
calcium carbonate (CaCO3) protects the underlying metal. This film retards dif-
fusion of dissolved oxygen to cathodic areas, supplementing the natural corrosion
barrier of Fe(OH)2 mentioned earlier (Section 7.2.3). In soft water, no such pro-
tective film of CaCO3 can form. But hardness alone is not the only factor that
determines whether a protective film is possible. Ability of CaCO3 to precipitate
on the metal surface also depends on total acidity or alkalinity, pH, and concen-
tration of dissolved solids in the water. For given values of hardness, alkalinity,
and total dissolved salt concentration, a value of pH, given the symbol pHs, exists
at which the water is in equilibrium with solid CaCO3. When pH > pHs, the
deposition of CaCO3 is thermodynamically possible.
Langelier divided natural fresh waters into two groups: those oversaturated
with CaCO3 and those undersaturated [32]. Since only near- or oversaturated
waters tended to form a protective film of CaCO3 on iron, an estimate of the
corrosivity of a water was established through analytical criteria for under- or
oversaturation. Using certain simplifications, Langelier showed that the value of
pHs—at which a water is in equilibrium with solid CaCO3 (neither tends to dis-
solve nor precipitate)—can be calculated from the relation*
2+
pH s = (pK 2′ − pKs′) + pCa + palk (7.16)
where K 2′ is the ionization constant (H + )(CO23−)/(HCO−3 ) , Ks′ is the solubility

product of calcium carbonate [(Ca 2+ )(CO23−)] , the concentration of calcium ions
(Ca2+) is in moles/1000 g H2O, and alk (alkalinity) represents the equivalents per
liter of titratable base to the methyl orange end point (often reported as ppm
CaCO3) according to the relation
(alk) + (H + ) → 2CO23− + HCO3− + OH −
The letter p refers to the negative logarithm of all these quantities. The saturation
index, also known as the Langelier index, is defined as the difference between
the measured pH of a water and the equilibrium pHs for CaCO3, or
Saturation index = pH measured − pH s
A positive value of the saturation index indicates a tendency for the protective
CaCO3 film to form, whereas a negative value indicates that it will not form.
Charts (see Appendix, Section 29.3) and nomographs have been prepared to
obtain values of pHs for waters varying widely in composition and at various
temperatures [33].
*For a derivation of this and a more exact equation, see Section 29.3 in the Appendix.
Tabulated data, originally organized by Nordell, for calculating the Langelier

saturation index are presented in Table 7.3 [34, 35].
After studying hundreds of concentrated cooling waters, Puckorius and
Brooke [36] proposed a new index, the practical saturation index (PSI),
PSI = 2 pH s − pH e
pH e = 1.485 × log (total alkalinity) + 4.54
CaCO3 precipitates at PSI < 6.0, according to Puckorius and Brooke.

An estimate of over- or undersaturation can also be obtained in the labora-
tory by measuring the pH of a water before and after exposure to pure CaCO3
powder for a time adequate to achieve equilibrium. An increase in pH corre-
TABLE 7.3. Data for Calculating the Langelier Saturation Index [34, 35]
Total Dissolved A Ca Hardness C M. O. Alkalinity D
Solids (ppm) (ppm as CaCO3) (ppm as CaCO3)
50–300 0.1 10–11 0.6 10–11 1.0

400–1000 0.2 12–13 0.7 12–13 1.1
14–17 0.8 14–17 1.2
18–22 0.9 18–22 1.3
Temperature (°C) B 23–27 1.0 23–27 1.4
28–34 1.1 28–35 1.5
0–1.1 2.6 35–43 1.2 36–44 1.6
2.2–5.6 2.5 44–55 1.3 45–55 1.7
6.7–8.9 2.4 56–69 1.4 56–69 1.8
10.0–13.3 2.3 70–87 1.5 70–88 1.9
14.4–16.7 2.2 88–110 1.6 89–110 2.0
17.6–21.1 2.1 111–138 1.7 111–139 2.1
21.2–26.7 2.0 139–174 1.8 140–176 2.2
27.8–31.1 1.9 175–220 1.9 177–220 2.3
32.2–36.7 1.8 230–270 2.0 230–270 2.4
37.8–43.3 1.7 280–340 2.1 280–350 2.5
44.4–50.0 1.6 350–430 2.2 360–440 2.6
51.1–55.6 1.5 440–550 2.3 450–550 2.7
56.7–63.3 1.4 560–690 2.4 560–690 2.8
64.4–71.1 1.3 700–870 2.5 700–880 2.9
72.2–81.1 1.2 880–1000 2.6 890–1000 3.0
1. Obtain values of A, B, C, and D from this table.

2. pHs = (9.3 + A + B) − (C + D).
3. Langelier saturation index = pH–pHs.
136 IRON AND STEEL
sponds to undersaturation. Because the composition of the water is altered by

any CaCO3 taken up or precipitated during the test, the final pH is not necessarily
the same as the calculated pHs. Alternatively, the water after saturation with
CaCO3 can be titrated with acid, with the increase in required milliliters of acid
compared to that required by the original water being a measure of undersatura-
tion (marble test) [37].
Any fresh water can be placed in one of the following categories:
Saturation Index Saturation Level Characteristic of Water

Positive Oversaturated with Protective film of
respect to CaCO3 CaCO3 forms
Zero In equilibrium
Negative Undersaturated with Corrosive
respect to CaCO3
Chicago water, for example, has an index of 0.2, whereas the value for Boston
water is −3.0.
A soft water with negative saturation index can usually be treated with lime,
sodium carbonate, or sodium hydroxide, in order to raise the saturation index to
a positive value, thereby making the water less corrosive. For very soft waters,
the required pH may be too high for uses such as tap water unless Ca2+ ions are
added simultaneously. A saturation index of +0.1 to about +0.5 is considered to
be satisfactory to provide corrosion protection. At higher values of the saturation
index, excessive deposition of CaCO3 (scaling) can occur, particularly at elevated
temperatures. Waters with a slightly negative Langelier index may deposit CaCO3
because of pH fluctuations. In general, for waters of negative saturation index,
the more negative the index, the more corrosive the water. The relationship
between the Langelier index and the corrosion rates of water pipes from a field
test at a city water works is presented in Fig. 7.12 [38, 39].
At above-room temperatures, the saturation index may become more posi-
tive, and, in any case, the rate of CaCO3 deposition is higher, should there be
any tendency toward deposition. Hence, corrosion protection at all temperatures
without excessive scaling requires adjustment of water composition to a satura-
tion index that is at least constant over the entire operating temperature range.
Powell et al. [33, 40] showed that, for any specific alkalinity, there is a correspond-
ing pH value at which the decrease of measured pH with temperature is almost
exactly compensated by a decrease in the factor ( pK 2′ − pKs′ ) . Under these condi-
tions, the saturation index is nearly constant with temperature, and scaling tends
to be the same in hot or cold water (Table 7.4). The amount of possible scaling,
of course, depends on the value of the saturation index. The alkalinity and the
pH of waters can be adjusted to bring them into the proper composition range
using Ca(OH)2, Na2CO3, NaOH, H2SO4, or CO2.
Figure 7.12. Relationship between the Langelier index and the corrosion rates of water
pipes. (Reproduced from Fujii [39] with permission of Japan Association of Corrosion
Control.)
TABLE 7.4. Alkalinity–pH Limits for Uniform Scale

Deposition at Various Temperatures [40]
Alkalinity (ppm as CaCO3) pH Measured at
Room Temperature
50 8.10–8.65
100 8.60–9.20
150 8.90–9.50
200 8.90–9.70
Limitations of Saturation Index. If a natural water contains colloidal silica

or organic matter (e.g., algae), CaCO3 may precipitate on the colloidal or organic
particles instead of on the metal surface. If such is the case, the corrosion rate
will remain high even though the saturation index is positive. For waters high in
dissolved salts, such as NaCl, or for waters at elevated temperatures, the CaCO3
film may lose its protective character at local areas, resulting in corrosion pitting.
Furthermore, if complexing ions are added to a chemically treated water, such
as polyphosphates, which retard precipitation of CaCO3, the saturation index
may no longer apply as an index of corrosivity.
Other than these exceptions, the saturation index is a useful qualitative guide
to the relative corrosivity of a fresh water in contact with metals for which the
corrosion rate depends on diffusion of dissolved oxygen to the surface, such as
iron, copper, brass, and lead. The index does not apply to corrosivity of a water
138 IRON AND STEEL
in contact with passive metals that corrode less the higher the surface concentra-
tion of oxygen, such as aluminum and the stainless steels.
7.3 METALLURGICAL FACTORS
7.3.1 Varieties of Iron and Steel

As discussed in Section 7.2.3, the corrosion rate of iron and steel in natural waters
is controlled by diffusion of oxygen to the metal surface. Hence, whether a steel
is manufactured by the Bessemer, oxygen furnace, or open-hearth process, as
well as whether it is a wrought iron or a cast iron, makes little or no difference
to the corrosion rate in natural waters, including seawater [16]. The same state-
ment applies to corrosion in a variety of soils, because factors determining the
corrosion rate underground are similar to those of total submersion. In general,
therefore, the least expensive steel or iron of a given cross-sectional thickness
having the required mechanical properties is the one that should be specified for
those environments.
On the other hand, in the acid range of pH (approximately <4) and probably
also in the extreme alkaline range (>13.5) where impurities play a role in the
hydrogen evolution reaction, differences in manufacture affect the corrosion
rate. A relatively pure iron corrodes in acids at a much lower rate than an iron
or steel high in residual elements, such as carbon, nitrogen, sulfur, and
phosphorus.
The high nitrogen content of Bessemer steel makes it more sensitive than
open-hearth steels to stress-corrosion cracking in hot caustic or nitrate solution.
For this reason, open-hearth steel is usually specified for boilers.
Cast iron in natural waters or in soils corrodes initially at the expected normal
rate, but may provide much longer service life than steel. Other than the factor
of considerable metal thickness common to cast structures, this advantage occurs
because cast iron, composed of a mixture of ferrite phase (almost pure iron) and
graphite flakes, forms corrosion products that, in some soils or waters, cement
together the residual graphite flakes. The resulting structure (e.g., water pipe),
although corroded completely, may have sufficient remaining strength, despite
low ductility, to continue functioning under the required operating pressures and
stresses. This type of corrosion is called graphitic corrosion. It occurs only with
gray cast iron (or “ductile” cast iron containing spheroidal graphite) but not with
white cast iron (cementite + ferrite). Graphitic corrosion can be reproduced in
the laboratory over a period of weeks or months by exposing gray cast iron to a
very dilute sulfuric acid that is renewed periodically.
7.3.2 Effects of Composition

Composition of an iron or steel within the usual commercial limits of carbon and
low-alloy steels has no practical effect on the corrosion rate in natural waters or
METALLURGIC AL FAC TORS 139
soils (see Table 7.1, Section 7.2.3; Table 10.1, Section 10.3). Only when a steel is
alloyed in the proportions of a stainless steel (>12% Cr) or a high-silicon iron or
high-nickel iron alloy for which oxygen diffusion no longer controls the rate,
is corrosion appreciably reduced. For atmospheric exposures, the situation is
changed because the addition of certain elements in small amounts (e.g., 0.1–1%
Cr, Cu, or Ni) has a marked effect on the protective quality of naturally formed
rust films (see Chapter 9).
Although carbon content of a steel has no effect on the corrosion rate in
fresh waters, a slight increase in rate (maximum 20%) has been observed in sea-
water as the carbon content is raised from 0.1 to 0.8% [41]. The cause of this
increase is probably related to greater importance of the hydrogen evolution
reaction in chloride solution (with complexing of Fe2+ by Cl−) supplementary to
oxygen depolarization as the cathodic surface of cementite (Fe3C) increases.
In acids, the corrosion rate depends on the composition as well as the struc-
ture of the steel and increases with both carbon and nitrogen content. The extent
of the increase depends largely on prior heat treatment (see Section 7.3.3) and
is greater for cold-worked steels (Fig. 8.2, Section 8.1). Statistical techniques
have been used to investigate the effects of minor alloying elements on the cor-
rosion characteristics of commercial carbon and low-alloy steels in 0.1 N H2SO4
at 30 °C [42]. For the particular steels studied, corrosion rates were increased with
increasing carbon content, especially in the range 0.5–0.7% C, and by
phosphorus.
Both alloyed sulfur and phosphorus markedly increase the rate of attack in
acids. These elements form compounds that apparently have low hydrogen over-
potential; in addition, they tend to decrease anodic polarization so that the cor-
rosion rate of iron is stimulated by these elements at both anodic and cathodic
sites. Rates in deaerated citric acid are given in Table 7.5 [43]. In strong acids,
the effects of these elements are still more pronounced [44] (see Fig. 7.13 and
Table 7.5).
Sulfide inclusions have been found to act as initiation sites for pitting corro-
sion of mild steels in neutral-pH solutions [45, 46]. On the other hand, sulfur
content has been found to have no significant effect on corrosion rates in acids
of steels containing more than 0.01% Cu [42].
TABLE 7.5. Corrosion Rates of Iron Alloys in Deaerated Citric Acid and in 4% NaCl + HCl
at 25 °C [43]
0.1 M Citric Acid pH = 2.06 4% NaCl + HCl pH = 1
Pure iron (0.005% C) 2.9 gmd 3.0 gmd

+0.02% P 16.5 100
+0.015% S 70.6 283
+0.11% Cu 4.1 39
+0.10% Cu + 0.03% P 37.6 60.6
+0.08% Cu + 0.02% S 3.2 18.6
140 IRON AND STEEL
Figure 7.13. Effect of alloyed phosphorus, sulfur, and silicon in iron on corrosion in deaer-
ated 0.1 N HCl, annealed specimens, 25 °C [44]. (Reproduced with permission. Copyright 1965,
The Electrochemical Society.)
Measurements of hydrogen permeation rates through cathodically polarized

mild steels containing elongated (FeMn)S inclusions show that H2S produced at
the metal surface by dissolution of inclusions promotes hydrogen entry into the
steels. Permeation rates increase with sulfur content of the steel in the range
0.002–0.24% S, but only where the H2S supply can be maintained by dissolution
of inclusions [47]. Elongated inclusions, most commonly manganese sulfide inclu-
sions, provide sites for initiation of hydrogen-induced cracking (HIC), also called
stepwise cracking (SWC), in steels that are used for high-pressure pipelines trans-
porting oil and natural gas [48, 49]. HIC is discussed further in Section 8.4.
Arsenic is present in some steels in small amounts. In quantities up to 0.1%,
it increases the corrosion rate in acids (less than sulfur and phosphorus); in large
amounts (0.2%), it decreases the rate [44].
Manganese, in amounts normally present, effectively decreases acid corro-
sion of steel containing small amounts of sulfur. Inclusions of MnS have low
electrical conductivity compared to FeS; in addition, manganese reduces the solid
solubility of sulfur in iron, thereby probably restoring the anodic polarization of
iron which is lowered by the presence of sulfur [50]. Silicon only slightly increases
the corrosion rate in dilute hydrochloric acid (Fig. 7.13).
Copper alloyed with pure iron to the extent of a few tenths of 1% moderately
increases the corrosion rate in acids. However, in the presence of phosphorus or
sulfur, which are normal components of commercial steels, copper counteracts
METALLURGIC AL FAC TORS 141
the accelerating effect of these elements. Copper-bearing steels, therefore, usually

corrode in nonoxidizing acids at lower rates than do copper-free steels [51]. The
data of Table 7.5 for several relatively pure iron alloys show that 0.1% Cu
reduces corrosion in 4% NaCl + HCl when 0.03% P or 0.02% S is present in the
iron, but not for the phosphorus alloy in citric acid. Addition of 0.25% Cu to a
low-alloy steel caused reduction of the corrosion rate from 1.1 to 0.8 mm/y in
0.5% acetic acid–5% sodium chloride solution saturated with hydrogen sulfide
at 25 °C [52]. These particular relations apply only to the specific compositions
and experimental conditions reported; they are not necessarily general. Steels
containing a few tenths of 1% of copper are more resistant to the atmosphere,
but show no advantage over copper-free steels in natural waters or buried in the
soil where oxygen diffusion controls the rate.
An amount up to 5% chromium (0.08% C) was reported to decrease weight
losses in seawater at the Panama Canal [53] at the end of one year. A sharp
increase in rates was observed between 2 and 4 years; after 16 years, the chro-
mium steels lost 22–45% more weight than did 0.24% C steel. Depth of pitting
was less for the chromium steels after one year, but comparable to pit depth in
carbon steel after 16 years. Hence, for long exposures to seawater, low-chromium
steels apparently offer no advantage over carbon steel. By comparison, however,
low-alloy chromium steels (<5% Cr) have improved resistance to corrosion
fatigue in oil-well brines free of hydrogen sulfide.
An amount up to 5% nickel (0.1% C) did not appreciably change weight
losses of steels exposed to seawater in tests at the Panama Canal [53] extending
up to 16 years. Depth of pits, although less for one year of exposure, was greater
for long-exposure times for the nickel steels compared to 0.24% C steel (77%
deeper for 5% Ni steel after 8 years). Low-nickel steels (<5% Ni) have improved
resistance to corrosion fatigue in oil-well brines containing hydrogen sulfide [54].
Nickel also decreases the corrosion rate of steels exposed to alkalies, and the
effect increases with nickel content [55].
7.3.2.1 Galvanic Effects through Coupling of Different Steels. Unim-

portant though low-alloy components may be in determining overall corrosion
rates in waters or in soils, composition is nevertheless of considerable importance
to the galvanic relations and consequent corrosion of steels coupled to each
other. For example, because of increased anodic polarization, a low-nickel, low-
chromium steel is cathodic to mild steel in most natural environments. The
reason is obvious from relations shown in Fig. 7.14. Both mild steel and a low-
alloy steel, not coupled, corrode at about the same rate, icorr, established by the
limiting rate of oxygen reduction. When coupled, however, the potentials of both
steels, which are originally different, become equal to φgalv. The corrosion rate of
mild steel, estimated from the extension of its anodic polarization curve, is now
increased to i2, and that of the low-alloy steel is decreased to i1. The precise value
of φgalv depends on the relative areas of the two steels. Accordingly, steel bolts
and nuts used to couple underground mild-steel pipes, or a weld rod used for
steel plates on the hull of a ship, should always be of a low-nickel, low-chromium
142 IRON AND STEEL
Figure 7.14. Polarization diagram showing effect of coupling of a low-alloy steel to mild
steel on subsequent corrosion rates.
steel or similar composition that is cathodic to the major area of the structure
(small cathode, large anode). Should the reverse polarity occur, serious corrosion
damage would be caused quickly either to the bolts or to the critical area of weld
metal [56, 57].
Cast iron is initially anodic to low-alloy steels and not far different in poten-
tial from mild steel. As cast iron corrodes, however, especially if graphitic cor-
rosion takes place, exposed graphite on the surface shifts the potential in the
noble direction. After some time, therefore, depending on the environment, cast
iron may achieve a potential cathodic to both low-alloy steels and mild steel. This
behavior is important in designing valves, for example. The trim of valve seats
must maintain dimensional accuracy and be free of pits; consequently, the trim
must always be chosen cathodic to the valve body making up the major internal
area of the valve. For this reason, valve bodies of steel are often preferred to cast
iron for aqueous media of high electrical conductivity.
7.3.3 Effect of Heat Treatment

A carbon steel quenched from high temperatures has a structure called martens-
ite—a supersaturated solution of carbon in iron—a single metastable phase with
carbon in solid solution in interstitial positions of the body-centered tetragonal
lattice of iron atoms. Random distribution of carbon atoms accompanied by
electronic interaction of carbon atoms with neighboring iron atoms limits their
effectiveness as cathodes of local-action cells; consequently, in dilute acid the
STEEL REINFORCEMENTS IN CONCRETE 143
corrosion rate of martensite is relatively low. Interstitial carbon reacts in large

part with acid to form a hydrocarbon gas mixture (accounting for the odor of
pickled steel) and some residual amorphous carbon, which is observed as a black
smut on the steel surface.
Heating martensite to low temperatures (below 727 °C) and then air-cooling
(called tempering) results in the formation of tempered martensite, which con-
sists of α-iron and many dispersed particles of cementite (i.e., iron carbide, Fe3C).
This two-phase structure of α-iron and cementite sets up galvanic cells that
accelerate the corrosion reaction. The amount of finely divided cementite that
forms depends on the tempering time and temperature; for a 2-h heat treatment
of 0.95% C steel, the maximum cementite forms at about 400 °C (300 °C for
0.07% C steel). After tempering at this temperature, cementite, acting as cathode,
offers maximum peripheral surface adjoining ferrite, and galvanic action during
subsequent exposure to an aqueous environment is at a maximum. Above this
temperature, cementite coalesces to larger particle size, and the subsequent cor-
rosion rate is lower. The particles of cementite are now large enough to resist
complete dissolution in acid and can be detected in the residue of corrosion
products. At the same time, there is a corresponding decrease in hydrocarbon gas
formation.
On slowly cooling a carbon steel from the austenite (face-centered cubic
lattice) region, above 727 °C, cementite, in part, assumes a lamellar shape, forming
a structure called pearlite. This structure again corrodes at a comparatively low
rate because of the relatively massive form of cementite formed by decomposi-
tion of austenite compared with smaller-size cementite particles resulting from
decomposition of martensite. Corrosion rate increases as the size of iron carbide
particles decreases. Pearlitic structures corrode faster than spheroidized ones,
and steels containing fine pearlite corrode more rapidly than those with coarse
pearlite [42]. The importance of both the amount of cementite acting as cathode
and its state of subdivision supports the electrochemical mechanism of corrosion.
The rate of corrosion is cathodically controlled and, hence, depends on hydrogen
overpotential and interfacial area of cathodic sites.
In practice, an effect of heat treatment on corrosion is seldom observed,
because oxygen diffusion controls the rate in the usual environments. However,
in handling acid oil-well brines, marked localized corrosion is sometimes found
near welds or “up-set” ends of steel oil-well tubing. This observed increase in
corrosion encircling a limited inner region of the tube is called ring-worm corro-
sion. It is caused by heat treatment incidental to joining and fabrication tech-
niques, and it can be minimized by a final heat treatment of the tubing or by
addition of inhibitors to the brine [58].
7.4 STEEL REINFORCEMENTS IN CONCRETE
Steel-reinforced concrete is an industrially very important system in which steel

is exposed to an alkaline (pH > 12) environment and, hence, is normally passive.
144 IRON AND STEEL
Nevertheless, corrosion of steel reinforcements does occur in structures such as

concrete bridge decks and parking garages. These problems have been studied
for many years and result from the breakdown of passivity caused, for example,
by salt in the environment or in the concrete [59]. Passivity may also be lost after
several years if air diffuses through the concrete to the reinforcements, convert-
ing alkaline Ca(OH)2 to less alkaline CaCO3. Corrosion processes for steel in
concrete are illustrated in Fig. 7.15 [60].
There are several methods that can be used to control corrosion of steel
reinforcements in concrete. First, the design of the structure should provide for
drainage of salt-containing waters away from the reinforced concrete. Second,
concrete of adequate thickness, high quality, and low permeability should be
specified to protect the reinforcements from the environment. Third, chloride
content of the concrete mix should be kept to a minimum. For further protection,
the steel reinforcements can be epoxy-coated. In many parts of North America,
steel reinforcements used in bridge decks are now epoxy-coated as a standard
construction procedure. Cathodic protection is also being used, both with
impressed current anodes and with sacrificial anodes [61]. (See Chapter 13.)
Steel reinforcements in concrete, being passive, are noble in potential with
respect to steel outside the concrete that is galvanically coupled to the reinforce-
ments. The measured potential difference is in the order of 0.5 V [62]. The effect
of large cathode area and small anode area has caused premature failures of
buried steel pipe entering a concrete building [63]. In this situation, use of epoxy-
coated reinforcements (to coat the cathode) or insulated couplings should prove
beneficial.
Figure 7.15. Corrosion process for steel in concrete [59]. (Reprinted with permission of John
Wiley & Sons, Inc.)
REFERENCES 145
There is evidence that high-strength steel reinforcements, such as rod or bar,

heat-treated to high hardness (Rockwell C > 40) and subjected to a tensile stress,
have failed by SCC or hydrogen cracking (see Chapter 8) through exposure to
moisture penetrating the concrete coating. Heat-treating processes sometimes
produce a decarburized (hence softer) surface layer. In this situation, SCC may
be delayed until the outer metal layer undergoes general corrosion, exposing the
SCC-susceptible harder core underneath. Either moisture must be excluded from
contact with such steels, or a steel of lower strength should be specified.
REFERENCES
1. I. Matsushima, in Uhlig’s Corrosion Handbook, 2nd edition, R. W. Revie, editor,

Wiley, New York, 2000, p. 529.
2. H. Uhlig, D. Triadis, and M. Stern, J. Electrochem. Soc. 102, 59 (1955).
3. H. Uhlig, J. Electrochem. Soc. 108, 327 (1961).
4. B. J. Little and J. S. Lee, Microbiologically influenced Corrosion, Wiley Series in Cor-
rosion, R. W. Revie, series editor, Wiley, New York, 2007, p. 1.
5. J.-D. Gu, T. E. Ford, and R. Mitchell, in Uhlig’s Corrosion Handbook, 2nd edition,
edited by R. W. Revie, Wiley, New York, 2000, pp. 349–365, 915–927.
6. Ref. 4, p. 41.
7. C. von Wolzogen Kühr, Water and Gas 7, 26, 277 (1923); Corrosion 17, 293t (1961).
8. Ref. 4, pp. 28–30.
9. R. Schweisfurth and E. Heitz, Mikrobiologische Materialzerstoerung und Materi-
alschutz, DECHEMA, Frankfurt am Main, Germany, 1989.
10. Ref. 5, pp. 359–360.
11. G. Skaperdas and H. Uhlig, Ind. Eng. Chem. 34, 748 (1942).
12. W. Whitman, R. Russell, and V. Altieri, Ind. Eng. Chem. 16, 665 (1924).
13. I. Matsushima, Ref. 1, pp. 536–538.
14. R. Scholder, Angew. Chem. 49, 255 (1936).
15. W. Whitman and R. Russell, Ind. Eng. Chem. 16, 276 (1924).
16. F. LaQue, Am. Soc. Testing Mater. Proc. 51, 495 (1951).
17. W. Whitman and R. Russell, Ind. Eng. Chem. 17, 348 (1925).
18. A. P. Bond, Sc.D. thesis, Department of Metallurgy, M.I.T., Cambridge, MA, 1958.
19. W. Whitman, R. Russell, C. Welling, and J. Cochrane, Ind. Eng. Chem. 15, 672 (1923).
20. Z. Foroulis and H. Uhlig, J. Electrochem. Soc. 111, 13 (1964).
21. R. Russell et al., Ind. Eng. Chem. 19, 65 (1927).
22. F. LaQue, in Corrosion Handbook, H. H. Uhlig, editor, Wiley, New York, 1948,
p. 391.
23. F. Speller and F. LaQue, Corrosion 6, 209 (1950).
24. J. Postlethwaite and S. Nesic, in Uhlig’s Corrosion Handbook, 2nd edition, R. W. Revie,
editor, Wiley, New York, 2000, p. 261.
25. Ibid., p. 262.
146 IRON AND STEEL
26. Ibid., pp. 267–269.

27. B. Angell, in Corrosion, 3rd edition, L. L. Shreir, R. A. Jarman, and G. T. Burstein,
editors, Butterworth-Heinemann, Oxford, U.K., 1994, pp. 8:197–8:207.
28. W. Leith and A. Thompson, Trans. Am Soc. Mech. Eng., J. Basic Eng. December, 795
(1960).
29. C. Borgmann, Ind. Eng. Chem. 29, 814 (1937).
30. O. Bauer, O. Kröhnke, and G. Masing, Die Korrosion metallischer Werkstoffe, Vol. 1,
S. Hirzel, Leipzig, 1936, p. 240.
31. G. Schick and H. Uhlig, J. Electrochem. Soc. 111, 1211 (1964).
32. W. F. Langelier, J. Am. Water Works Assoc. 28, 1500 (1936).
33. S. Powell, H. Bacon, and J. Lill, Ind. Eng. Chem. 37, 842 (1945).
34. Ref. 1, p. 534.
35. E. Nordell, Water Treatment for Industrial and Other Uses, 2nd edition, Reinhold, New
York, 1961, p. 287.
36. P. R. Puckorius and J. M. Brooke, Corrosion 47, 280 (1991).
37. C. P. Hoover, J. Am. Water Works Assoc. 30, 1802 (1938).
38. Ref. 1, p. 535.
39. T. Fujii, Bosei Kanri (Rust Prevention and Control) 27, 85 (1983).
40. S. Powell, H. Bacon, and J. Lill, J. Am. Water Works Assoc. 38, 808 (1946).
41. C. Chappell, J. Iron Steel Inst. 85, 270 (1912).
42. H. Cleary and N. D. Greene, Corros. Sci. 7, 821 (1967).
43. M. Stern, J. Electrochem. Soc. 102, 663 (1955).
45. L. J. Gainer and G. R. Wallwork, Corrosion 36, 348 (1980).
46. Y.-Z. Wang, R. W. Revie, and R. N. Parkins, CORROSION/99, Paper No. 143, NACE
International, Houston, TX, 1999.
47. P. H. Pumphrey, Corrosion 36, 537 (1980).
48. M. Elboujdaini, in Uhlig’s Corrosion Handbook, 2nd edition, R. W. Revie, editor,
49. B. E. Wilde, C. D. Kim, and E. H. Phelps, Corrosion 36, 625 (1980).
50. G. Wranglen, Corros. Sci. 9, 585 (1969).
51. E. Williams and M. Komp, Corrosion 21, 9 (1965).
52. Y. Yoshino, Corrosion 38, 156 (1982).
53. C. Southwell and A. Alexander, Mater. Prot. 9, 14 (1970).
54. B. B. Wescott, Mech. Eng. 60, 813 (1938).
55. F. L. LaQue and H. R. Copson, editors, Corrosion Resistance of Metals and Alloys,
Reinhold, New York, 1963, p. 334.
56. E. Uusitalo in Proc. 2nd International Congress on Metallic Corrosion, National Asso-
ciation of Corrosion Engineers, Houston, Texas, 1966, p. 812.
57. R. J. Brigham, M. McLean, V. S. Donepudi, S. Santyr, L. Malik, and A. Garner, Can.
Metall. Q. 27(4), 311 (1988).
58. M. Holmberg, Corrosion 2, 278 (1946); R. Manuel, Corrosion 3, 415 (1947).
PROBLEMS 147
59. J. P. Broomfield, in Uhlig’s Corrosion Handbook, 2nd edition, R. W. Revie, editor,

60. Ibid., p. 582.
61. J. Broomfield, Mater. Perf. 46(1), 26 (2007).
62. J. Vrable, Mater. Perf. 21(3), 51 (1982).
63. I. Matsushima, private communication.
GENERAL REFERENCES
H. Ahluwalia, Highway Bridges Gap Analysis, Report for NACE International,

Houston, Texas, August 14, 2007, http://www.nace.org/nace/images_ndx_story/
highwaybridgegapanalysis.pdf.
Neal S. Berke, Edward Escalante, Charles K. Nmai, and David Whiting, Editors, Techniques
to Assess the Corrosion Activity of Steel Reinforced Concrete Structures, STP 1276,
ASTM, West Conshohocken, PA, 1996.
S. W. Borenstein, Microbiologically Influenced Corrosion Handbook, Woodhead Publish-
ing, Cambridge, England, 1994.
J. P. Broomfield, Corrosion of steel in concrete, in Uhlig’s Corrosion Handbook, 2nd
J. P. Broomfield, Corrosion of Steel in Concrete: Understanding, Investigation and Repair,
2nd edition, Taylor & Francis, London, 2007.
Corrosion of ferrous metals, in ASM Handbook, Vol. 13B: Corrosion: Materials, ASM
International, Materials Park, OH, 2005, pp. 1–53.
J.-D. Gu, T. E. Ford, and R. Mitchell, Microbial degradation of materials: General pro-
cesses, in Uhlig’s Corrosion Handbook, 2nd edition, R. W. Revie, editor, Wiley, New
York, 2000, pp. 349–365.
J. R. Kearns and B. J. Little, editors, Microbiologically Influenced Corrosion Testing, STP
1232, ASTM, Philadelphia, PA, 1994.
B. J. Little and J. S. Lee, Microbiologically influenced Corrosion, Wiley Series In Corro-
sion, R. W. Revie, series editor, Wiley, Hoboken, NJ, 2007.
P. R. Roberge, Corrosion inspection and MonitorIng, Wiley Series In Corrosion, R. W.
Revie, series editor, Wiley, New York, 2007, pp. 373–376.
Uhlig’s Corrosion Handbook, 2nd edition, R. W. Revie, editor, Wiley, New York, 2000,
pp. 515–600.
PROBLEMS
1. Five iron rivets, 0.5 in.2 (3.2 cm2) of total exposed area each, are inserted in a
copper sheet of 8 ft2 (7430 cm2) exposed area. The sheet is immersed in an
aerated, stirred, conducting solution in which uncoupled iron corrodes at
0.0065 ipy (0.165 mm/y).
148 IRON AND STEEL
(a) What is the corrosion rate of the rivets in ipy (mm/y)?

(b) What is the corrosion rate of an iron sheet in which five copper rivets are placed,
with the same dimensions?
2. Water entering a steel pipeline at the rate of 40 liters/min contains 5.50 mL

O2 per liter (25 °C, 1 atm). Water leaving the pipe contains 0.15 mL O2 per
liter. Assuming that all corrosion is concentrated at a heated section 30 m2 in
area forming Fe2O3, what is the corrosion rate in gmd?
3. Two steels immersed in dilute deaerated sulfuric acid corrode at different

rates. When they are arranged as a cell, a small potential difference is observed
between them. Which is anode? Illustrate by a polarization diagram.
4. Calculate the saturation index of each of the following waters at:

(a) 25 °C (77 °F) using Eq. (7.16) in Section 7.2.6.1;
(b) 25 °C (77 °F) using chart Fig. 29.4, Section 29.3;
(c) 75 °C (167 °F) using charts. (Note that the calcium concentration is listed in the
chart as ppm CaCO3.)
Water Alkalinity Ca pK 2′ − pKS′ pH Total Solids

(ppm CaCO3) (ppm) (ppm)
Boston, MA 13 5 2.2 6.90 43
Chicago, IL 120 34 2.3 8.0 157
Detroit, MI 73 26 2.2 7.7 153
Answers to Problems
1. (a) 3.0 ipy (77 mm/y).
2. 31.3 gmd.
3. Slower corroding steel is anode.
4. Water Saturation Index
(Using Charts)
25 °C 75 °C
Boston, MA −2.7 −2.2

Chicago, IL 0.2 0.6
Detroit, MI −0.5 −0.1
8
EFFECT OF STRESS
8.1 COLD WORKING
As discussed in Section 7.2, a cold-worked commercial steel corrodes in natural

waters at the same rate as an annealed steel. In acids, however, cold working
increases the corrosion rate severalfold, as shown in Fig. 8.1 [1]. Many authors
have traditionally ascribed this effect to residual stress within the metal, which
serves to increase the corrosion tendency. But the residual energy produced by
cold working, as measured in a calorimeter (usually <30 J/g), is less than sufficient
to account for an appreciable change in free energy; hence, this intuitive concept
is probably not correct [2]. The observed increase of rate is apparently caused
instead by segregation of carbon or nitrogen atoms at imperfection sites pro-
duced by plastic deformation rather than by the presence of the imperfections
themselves (Fig. 8.2). Such sites exhibit lower hydrogen overpotential than does
either cementite or iron [1] and probably constitute the most important factor.
Entering to a lesser extent are (1) increased surface area of metal exposed at slip
steps, (2) the increased surface area of cementite lamellae fractured by the cold-
work process, and (3) the preferred orientation of ferrite grains, with the latter
either increasing or decreasing corrosion depending on the particular crystal
faces that lie parallel to the metal surface.

149
150 EFFECT OF STRESS
Figure 8.1. Effect of heat treatment of cold-worked 0.076% C steel (85% reduction of thick-
ness) and zone-refined iron (50% reduction of thickness) on corrosion in deaerated 0.1N HCl,
25°C [1]. (Reproduced with permission. Copyright 1964, The Electrochemical Society.)
Subsequent heat treatment of cold-worked steel at 100°C induces additional

diffusion of interstitial carbon atoms to imperfections in the metal lattice, thereby
increasing the cathodic area of low hydrogen overvoltage and also accelerating
the corrosion rate. Heat treatment at higher temperatures reduces the density of
the imperfection sites, accompanied by precipitation of carbides or nitrides of
particle size that increases with heat treatment temperature. Hence, heat treat-
ment above 100°C results in cathodic sites of higher hydrogen overpotential and
of decreasing peripheral area, leading to a corresponding reduction of corrosion
rate. A severely cold-worked, zone-refined (pure) iron, on the other hand, lacking
sufficient carbon or nitrogen, corrodes in dilute, deaerated hydrochloric acid at
no higher rate than when annealed (Figs. 8.1 and 8.2) [1].
When commercial nickel is severely cold-worked, unlike mild steel, it does
not corrode appreciably more rapidly in acids [2], which suggests that similar
formation of low-overpotential cathodic sites derived from segregated, interstitial
impurities does not occur.
8.2 STRESS-CORROSION CRACKING
Stress-corrosion cracking (S.C.C.) is a type of cracking that occurs when a mate-

rial that is susceptible to S.C.C. is simultaneously stressed in tension and exposed
to an environment that causes S.C.C. On a macroscopic level, S.C.C. failures
appear to be brittle; that is, the usual ductility of the material (e.g., when stressed
in air) is considerably reduced. The tensile stress can be applied or residual, or
STRESS-CORROSION CR ACKING 151
Figure 8.2. Effect of carbon in steels cold-rolled 50%, or subsequently annealed, on corro-
sion in deaerated 0.1N HCl, 25°C [1]. (Reproduced with permission. Copyright 1964, The Elec-
trochemical Society.)
both. Residual stresses result from fabrication processes, such as deformation

(e.g., forming of a pipe) and welding. Stress-corrosion cracks can be intergranular
or transgranular, or a combination of the two. In general, there are three stages
in the stress-corrosion cracking process:
1. Generation of the environment that causes S.C.C. [3]

2. Initiation of S.C.C.
3. Propagation of S.C.C. until failure occurs
Depending on the metal–environment combination and the stressing condition,

the time to failure can vary from minutes to many years. For this reason, inspec-
tion of stressed metals that are exposed to a corrosive environment during service
is essential to establish whether cracks have initiated and to develop mitigation
procedures before failure occurs.
Table 8.1 lists some alloy–environment combinations in which S.C.C.
occurs.
Stress-corrosion cracking is caused by the interaction of metallurgical,
mechanical, and environmental factors, with the result that there is a multiplicity
of possible S.C.C. control measures that can be implemented. In addition, the
complexity of S.C.C. has led to a very large number of hypotheses, models, theo-
ries, and controversies on the mechanisms by which S.C.C. occurs. These matters
will be summarized in this section.
8.2.1 Iron and Steel

When mild steel is stressed in tension to levels near or beyond the elastic limit
and is exposed simultaneously to hot concentrated alkaline or hot concentrated
TABLE 8.1. Some Alloy–Environment S.C.C. Systems

Metal Environment
Mild steel NO−3 , OH−

High-strength steelsa H2O
Stainless steels, austenitic Cl−, OH−, Br−
α-Brass NH3, amines
Titanium alloys
8% Al, 1% Mo, 1% V Cl−, Br−, I−
Aluminum alloys H2O, NaCl solutions
Zirconium alloys Cl−
Magnesium alloys Cl−
<40 at.% Au–Cu FeCl3, aqua regia
a
>180,000 psi (>1240 MPa) yield strength or approximately >Rock-
well C 40 hardness value. Includes high-strength martensitic and
precipitation-hardening stainless steels.
nitrate solutions [such as boiling 60% Ca(NO3)2 + 3% NH4NO3], it cracks along

intergranular paths by S.C.C. The mechanism is quite different from that described
in Section 8.1.
Stress-corrosion cracking of steel was first encountered in a practical way in
riveted steam boilers. Stresses at rivets always exceed the elastic limit, and boiler
waters are normally treated with alkalies to minimize corrosion. Crevices between
rivets and boiler plate allow boiler water to concentrate, until the concentration
of alkali suffices to induce S.C.C., sometimes accompanied by explosion of the
boiler. Because alkalies were recognized as one of the causes, failures of this kind
were first called caustic embrittlement. With the advent of welded boilers and with
improved boiler-water treatment, S.C.C. of boilers has become less common. Its
occurrence has not been eliminated entirely, however, because significant stresses,
for example, may be established at welded sections of boilers or in tanks used
for storing concentrated alkalies.
The presence of silicates in alkaline boiler water above 225°C accelerates
S.C.C., whereas at lower temperatures silicates may act as inhibitors [4]. Labora-
tory tests in boiling 50% NaOH have shown that at atmospheric pressure, 0.2–
1.0% PbO, KMnO4, Na2CrO4, or NaNO3 are also accelerators [4]. At the higher
temperatures and pressures common to boiler conditions, nitrates added in
amounts equivalent to 20–40% of NaOH alkalinity act as inhibitors of S.C.C. [4]
and are used for this purpose in practice. On the other hand, addition of 2%
NaOH to boiling nitrate solutions may inhibit cracking [5]. This is one of several
illustrations that can be cited regarding the necessity to understand thoroughly
the fundamentals of a laboratory test before extrapolating results to large-scale
applications.
In addition to failures in the chemical and nuclear-chemical [6, 7] industries
in handling hot nitrate solutions, stressed steel may also fail in contact with
nitrates at room temperature. Such failure occurred, for example, in 0.7% C steel
cables of the Portsmouth, Ohio, bridge after 12 years in service [8]. The cables
cracked at their base where rain water, presumably containing trace amounts of
ammonium nitrate from the atmosphere, had accumulated and concentrated.
Subsequent tests conducted at the U.S. National Bureau of Standards (now the
National Institute for Standards and Technology) showed that specimens of the
cable stressed in tension failed within 3 21 –9 21 months when immersed in 0.01N
NH4NO3 or NaNO3 at room temperature. No cracking occurred after similar tests
in distilled water, or in 0.01N solutions of NaCl, (NH4)2SO4, NaNO2, or NaOH.
There was evidence in this case that the steel cable was unusually susceptible to
S.C.C.
Stress-corrosion cracking of steel also occurs when the metal is in contact
with anhydrous liquid ammonia at room temperature—for example, at cold-
formed heads and at welds of steel tanks used to contain the liquefied gas. Cracks
are intergranular, but they can also be transgranular. Cracking can be avoided
by stress-relief heat treatment of the steel, by avoiding air contamination of the
NH3, or by addition of about 0.2% H2O, which acts as an inhibitor [9]. Intergranu-
lar cracking of stressed steel has also been reported in contact with SbCl3 + HCl
+ AlCl3 in a hydrocarbon solvent [10].
Transgranular S.C.C. was reported at room temperature on exposure of 0.1–
0.2% C steel to an aqueous mixture of carbon dioxide and carbon monoxide at
100 psi [11]. Cathodic polarization in the latter solution prevented damage. Explo-
sions have been reported involving cracks in steel tanks containing compressed
illuminating gas. The failures at stresses below the elastic limit were transgranular
and were traced to small amounts of HCN contained in the gas [12]. The problem
was solved by removing traces of HCN and moisture from the gas.
Underground steel pipelines that transmit oil and gas and that operate at
high internal pressures have been reported to fail by S.C.C. Both transgranular
and intergranular S.C.C. of pipeline steels have been reported [13, 14].
Based on tests in boiling nitrate solution [15], it was found that severely
cold-worked mild steel (0.06% C, 0.001% N) is resistant to S.C.C. (Fig. 8.3).
Along these lines, it is recognized in practice that cold-drawn steel wire is more
resistant to S.C.C. than is oil-tempered wire having equal mechanical properties.
Heat treatment of cold-rolled mild steel at 600°C (1110°F) for 1/2 h, at 445°C
(830°F) for 48 h, or at lower temperatures for correspondingly longer times
induces susceptibility again. Therefore, plastically deformed steel, stress-relieved
in the range of 400–650°C (750–1200°F) and subsequently stressed, is more
rather than less susceptible as a result of heat treatment. Mild steel quenched at
900–950°C (1650–1740°F) is susceptible, but can be made resistant by tempering
at 250°C (480°F) for 21 h (Fig. 8.3), or at 200°C (390°F) for 48 h, even if the steel
exposed to nitrates is highly stressed after heat treatment. This resistant state,
however, is temporary; on further heating (in the unstressed state) at 445°C
(830°F) for 70 h or at 550°C (1020°F) for 3 h, as well as for correspondingly
shorter times at higher temperatures, the steel becomes susceptible again and
remains susceptible.
Figure 8.3. Effect of heat treatment of mild steel after quenching or cold rolling (70%
reduction of thickness) on resistance to stress-corrosion cracking in boiling nitrate solution
[15]. (Reprinted with permission of ASM International®. All rights reserved. www.asminterna
tional.org.)
The overall evidence suggests that grain boundaries become suitable crack
paths only when carbon (or nitrogen) atoms (not Fe3C) segregate at grain-
boundary regions. Pure iron is immune to S.C.C. Iron (>0.002% C) [16] or mild
steel (0.06% C) quenched from about 925°C contains a sufficient concentration
of carbon atoms along the grain boundaries to induce susceptibility. Low-
temperature heating (e.g., 250°C for 21 h) randomly nucleates iron carbides, which
rob the grain boundaries of carbon, accounting for increased resistance or immu-
nity. Longer heating at higher temperatures (e.g., 70 h at 445°C) allows slow-
moving lattice imperfections within the grain to migrate to the grain boundaries,
transporting carbon atoms with them, and the steel again becomes susceptible.
Cold working, on the other hand, produces immunity by destroying continuous
grain-boundary paths, and, more important, by generating imperfections that
have high affinity for carbon and that deplete any continuous paths along which
carbon atoms tend to segregate.
Remedial measures to avoid S.C.C. of steel in nitrate solutions include the
following:
1. Severe Cold Working. Cold rolling to >50% reduction of thickness imparts

relative immunity to a stressed mild steel in boiling nitrate solution. The
resistant state is predicted to persist at low temperatures [e.g., 100–200°C
(200–400°F)], for thousands of hours.
2. Heat Treatment. Mild steel slowly cooled at 900–950°C (1650–1740°F), or
quenched from this temperature range and then tempered at about 250°C
(480°F) for 21 h, or at higher temperatures for shorter times, is resistant.
This resistance is temporary and short-lived (200 h) at temperatures on
the order of 400°C (750°F), but it is predicted to reach the order of thou-
sands of hours at 300°C (570°F) or below [15].
3. Surface Peening or Shot Blasting. Compressive stresses are produced at
the surface of the metal that are effective in avoiding damage so long as
the compressive layers are continuous, remain intact, and are not dissolved
by corrosion.
4. Cathodic Protection. Schroeder and Berk [4] found that cathodic polar-
ization of steel stressed in hot sodium hydroxide–sodium silicate solution
greatly delayed or prevented cracking. Parkins [17] found similar protec-
tion in hot nitrate solution. Bohnenkamp [18] reported maximum suscep-
tibility of various carbon steels (0.003–0.11% C) in 33% NaOH boiling at
120°C at −0.66 to −0.75 V (S.H.E.) with orders-of-magnitude longer life
at potentials at 0.1 V either noble or active to this range. Both anodic
and cathodic protection were found to be effective (see Fig. 8.7, Section
8.3.3).
5. Special Alloys. Steels containing small alloying additions of aluminum,
titanium, or niobium plus tantalum [19], which react preferentially with
carbon and nitrogen, exhibit improved resistance to S.C.C., but are not
immune. Alloyed additions of <2% Ni increase susceptibility of low-carbon
steels in nitrates; >1% Cr or Mo decrease susceptibility. Furnace-cooled
(pearlitic) steels of >0.2% C are resistant [20].
6. Inhibitors. Sodium nitrate has already been mentioned as a practical
inhibitor for steel exposed to boiler waters. Crude quebracho extract and
waste sulfite liquor are also used. Buffer ions, such as PO3− 4 , are useful
because they avoid high concentrations of OH− in concentrated boiler
water. In accelerated tests, the addition of 3% NaCl or 2% sodium acetate
to boiling 60% Ca(NO3)2 + 3% NH4NO3, at 108°C was found to inhibit
cracking (>200 h) [21] of mild steel.
The various approaches to S.C.C. control are presented in Table 8.2 [22]. The
dependence of S.C.C. on metallurgical, mechanical, and environmental variables
results in three main avenues for S.C.C. control:
Metallurgical: Use an alloy that is resistant to S.C.C.

Mechanical: Reduce the applied stress and/or stress-relief anneal to reduce
the residual stress.
TABLE 8.2. Stress-Corrosion Cracking Control Measures [22]

Mechanical Metallurgical Environmental
Avoid stress concentrators Change alloy composition Modify the environment
Relieve residual stresses Change alloy structure Apply anodic or cathodic
Introduce surface Use metallic or conversion protection
compressive stresses coating Add inhibitor
Reduce operating stresses Use organic coating
Design for nondestructive Modify temperature
inspection
Environmental: Change the environment or eliminate the environment from

contact with the metal surface by using a coating; apply electrochemical
protection (cathodic or anodic, depending on the system).
8.3 MECHANISMS OF STRESS-CORROSION CRACKING OF STEEL

AND OTHER METALS
The distinguishing characteristic of S.C.C. is the requirement of tensile stress

acting conjointly with a specific environment. Typical specific environments for
several metals are listed in Table 8.1 in Section 8.2. The damaging anions have
no clear relation to general corrosion rates of the metals that they affect. Chloride
ions, but not nitrate ions, cause S.C.C. of 18–8 austenitic stainless steels (contain-
ing 74% Fe), but the opposite situation applies to mild steel. The necessity for a
tensile stress is illustrated by the sensitivity of 70% Cu–30% Zn brass to inter-
granular corrosion (not requiring stress) in a variety of electrolytes, such as dilute
H2SO4, Fe2(SO4)3, or BiCl3 solutions [23]. The much more rapid S.C.C., which is
usually also intergranular, occurs in the presence of NH3 or amines. Furthermore,
an improperly heat-treated 18–8 stainless steel (e.g., sensitized at 650°C for 1 h)
fails intergranularly in a wide variety of electrolytes regardless of whether it is
stressed; but the same heat-treated steel stressed in tension and placed in a
boiling solution of magnesium chloride fails transgranularly by S.C.C. despite
well-defined corrosion paths along grain boundaries [24].
Following are five characteristics of S.C.C.:
1. Specificity of damaging chemical environments—not all environments

that cause corrosion also cause S.C.C.
2. General resistance or immunity of all pure metals. For many years, it was
understood that pure metals did not undergo S.C.C.; however, S.C.C. of
pure copper under aggressive laboratory conditions has been reported [25,
26]. Pure alloys, such as Cu–Zn, Cu–Au, and Mg–Al, on the other hand,
are susceptible.
MECHANISMS OF STRESS-CORROSION CR ACKING OF STEEL AND OTHER METALS 157
3. Successful use of cathodic polarization to avoid initiating S.C.C.

4. Inhibiting effect of various extraneous anions added to damaging environ-
ments. For example, 2% NaNO3, or 1% sodium acetate, or 3.5% NaI added
to magnesium chloride solution boiling at 130°C (33 g/100 mL) inhibits
S.C.C. of 18–8 stainless steel (>200 h) [27]. Similarly, Cl− or acetates inhibit
−
S.C.C. of mild steel in boiling nitrates [21], and SO2−4 or NO3 can be used
to inhibit a titanium alloy (8% Al, 1% Mo, 1% V) that otherwise cracks
in 3.5% NaCl solution at room temperature [28].
5. An appreciable effect of metallurgical structure; for example, ferritic stain-
less steels (body-centered cubic) are much more resistant to Cl− than are
austenitic stainless steels (face-centered cubic). Also, β and γ brass (>40%
Zn) may crack in water alone, but α brass (70% Cu, 30% Zn) fails in NH3
or an amine. Any metal of large grain size, whether failure is inter- or
transgranular, is more susceptible to S.C.C. than is the same metal of small
grain size.
Many models have been proposed to explain the mechanisms of S.C.C. at

atomic levels, but each of these models has its own limitations in that it can be
used to explain S.C.C. in a limited number of metal–environment systems.
Notwithstanding the absence of an accepted generalized model of S.C.C., a few
models are summarized in the following paragraphs.
8.3.1 Electrochemical Dissolution

Electrochemical dissolution is the basis for the film rupture model, also called the
slip–dissolution model. In 1940, Dix [29] proposed that galvanic cells are set up
between metal and anodic paths established by heterogeneous phases (e.g., CuAl2
precipitated from a 4% Cu–Al alloy) along grain boundaries or along slip planes.
When the alloy, stressed in tension, is exposed to corrosive environments, the
ensuing localized electrochemical dissolution of metal opens up a crack; in addi-
tion, the applied stress effectively ruptures brittle oxide films at the tip of the
crack, thereby exposing fresh anodic material to the corrosive medium. Support-
ing this mechanism was a measured potential of metal at grain boundaries that
was negative, or active, to the potential of grains. Furthermore, cathodic polariza-
tion prevented S.C.C. The film rupture model was used to explain transgranular
S.C.C. of copper in 1M NaNO2 solution [30].
If the crack growth rate is controlled by the rate of dissolution at the crack
tip, then the following equation can be used to estimate the crack growth rate,
da/dt:
da M
= ia ×
dt zFd
where ia is the anodic current density, M is the atomic weight of the metal, z is
the valency of the solvated species, F is Faraday’s constant, and d is the density
of the metal. Indeed, a correlation has been established for some systems between
crack growth rates and dissolution current densities on bare surfaces, providing
some basis for the credibility of this equation. The crack growth rate represented
by this equation is an upper limit of the crack growth rate by continuous dissolu-
tion since neither dissolution nor cracking is likely to take place continuously,
but rather will be interrupted by film growth at the crack tip until film rupture
takes place [31].
8.3.2 Film-Induced Cleavage

The film-induced cleavage model of S.C.C. is based on the following five steps:
1. A thin surface layer forms on the surface.

2. A brittle crack initiates in this layer.
3. The brittle crack crosses the film–metal-substrate interface with little loss
in velocity.
4. The brittle crack continues to propagate in the metal substrate.
5. After this crack becomes blunt and stops growing, this process repeats
itself.
This model can also be used to explain the crack arrest markings and cleavage-
like facets on the fracture surface, as well as the discontinuous nature of crack
propagation [32, 33], although more research into surface films and brittle frac-
ture is required before this model can be thoroughly evaluated [34].
8.3.3 Adsorption-Induced Localized Slip

The proponents of this model reasoned that similar fracture processes occur in
liquid-metal embrittlement, hydrogen embrittlement, and S.C.C., with chemisorp-
tion facilitating the nucleation of dislocations at the crack tip and promoting the
shear processes that result in brittle, cleavage-like fracture. It was found that
cleavage fracture occurs by alternate slip at the crack tip and formation of voids
ahead of the crack tip [35–37].
8.3.4 Stress Sorption

Figures 8.4 and 8.5 indicate the critical potentials noble to which S.C.C. of 18–8
stainless steel initiates when exposed to magnesium chloride solution boiling at
130°C with and without inhibiting anion additions [27]. Anodic polarization
induces shorter cracking times the more noble the controlled potential; cathodic
polarization, on the other hand, extends the observed cracking times. Below the
critical value of −0.145 V (S.H.E.), the alloy becomes essentially immune (Fig.
8.4). Addition of various salts, such as sodium acetate, to the magnesium chloride
solution shifts the critical potential to more noble values. When the amount of
Figure 8.4. Effect of applied potential on time to failure of stressed moderately cold-rolled
18–8 stainless steel in magnesium chloride solution boiling at 130°C [27]. (Reproduced with
Figure 8.5. Effect of applied potential on time to failure of stressed moderately cold-rolled
18–8 stainless steel in magnesium chloride solution with sodium acetate additions, boiling at
130°C (2% sodium acetate addition is inhibiting) [27]. (Reproduced with permission. Copyright
1969, The Electrochemical Society.)
added salt shifts the critical potential to a value that is noble to the corrosion
potential, S.C.C. no longer occurs (Fig. 8.5).
It was proposed [38, 39] that S.C.C., in general, proceeds not by electrochemi-
cal dissolution of metal, but instead by weakening of the cohesive bonds between
surface metal atoms through adsorption of damaging components of the environ-
ment. The name suggested for this mechanism is stress-sorption cracking. Since
chemisorption is specific, damaging components are also specific. The surface
energy of the metal is said to be reduced, increasing the tendency of the metal
to form a crack under tensile stress. Hence, the mechanism is related to the
Griffith criterion [40] of crack formation in glass and similar brittle solids, for
which the strain energy of the stressed solid must be greater than the total
increased surface energy generated by an incipient crack. Adsorption of any kind
that reduces surface energy should favor crack formation; hence, water adsorbed
on glass understandably reduces the stress needed to cause fracture.
The critical potential for S.C.C. is interpreted as that value above which
damaging ions adsorb on defect sites and below which they desorb. Such a poten-
tial, in principle, can be either active or noble to the corrosion potential. Inhibit-
ing anions, which of themselves do not initiate cracks, compete with damaging
species for adsorption sites, thereby making it necessary to apply a more positive
potential in order to reach a surface concentration of the damaging species ade-
quate for adsorption and cracking. Whenever the inhibiting anion drives the
critical potential above the corrosion potential, cracking no longer occurs; this is
because the damaging ion can no longer adsorb. The mechanism of competitive
adsorption parallels that describe earlier applying to the critical pitting potential,
which is also shifted in the noble direction by the presence of extraneous anions
(Section 6.6).
Stress-sorption cracking is the basic mechanism applying to stress cracking
of plastics by specific organic solvents [41, 42] and to liquid-metal embrittle-
ment—the cracking of solid metals by specific liquid metals. It is also the mecha-
nism proposed earlier by Petch and Stables [43] to account for stress cracking of
steel induced by interstitial hydrogen (see Section 8.4).
The mechanism of liquid-metal embrittlement is analogous to that of S.C.C.
in that only certain combinations of liquid metals and stressed solid metals result
in intergranular failure (Table 8.3) [44]. This specificity has important conse-
quences, one being that large-scale mercury boilers can be constructed of carbon
steel, but not of titanium or its alloys or of brass, because catastrophic intergranu-
lar failure would result. It is, apparently, possible for adsorbed mercury atoms to
reduce the metal bond strength within grain-boundary regions of stressed tita-
nium or brass adequate to cause failure, but this reduction of bond strength does
not occur for iron in this application.
TABLE 8.3. Susceptibilitya of Solid Metals to

Embrittlement by Liquid Metals [44]
Liquid → Li Hg Bi Ga Zn
Steel C NC NC NC C
Copper alloys C C C — —
Aluminum alloys NC C NC C C
Titanium alloys NC C NC NC NC
a
C = cracking; NC = no cracking.
8.3.5 Initiation of Stress-Corrosion Cracking and Critical Potentials

For various metals and solutions, values of critical potentials, immediately above
which (or noble to) S.C.C. initiates, are listed [45] in Table 8.4. Based on data
obtained for 18–8 stainless steel in MgCl2 at 130°C, cracks initiated to a depth
not greater than 0.013–0.025 cm (0.005–0.01 in.) stop propagating at a potential
5 mV or less below the critical value [46]. For deeper cracks, the imposed potential
necessary to stop propagation is increasingly negative (active), accounted for by
metallic shielding effects within the crack and by solution composition changes
resulting from factors like accumulation of anodic dissolution products within
the crack. In other words, the environmental conditions required to initiate a
crack are also those required for crack propagation.
For some metal–solution combinations, S.C.C. is avoided by polarizing not
only below a certain critical potential or potential range, but also at potentials
not far above (noble to) such a range. Failure times are most rapid at potentials
between those at which S.C.C. occurs. In the relatively narrow potential range
over which S.C.C. occurs, adsorption of damaging ions on mobile defect sites is
optimum, according to the stress-sorption viewpoint. For example, mild steel
undergoes pronounced intergranular S.C.C. in ammonium carbonate (170 g/liter)
at 70°C within the potential range −0.26 to −0.35 V (S.H.E.), but much less so
outside this range (Fig. 8.6) [47]. The susceptible range of potentials is still more
restricted for slightly cold-rolled steel. Since the corrosion potential is more noble
TABLE 8.4. Some Critical Potentials for Initiation of S.C.C. [45]

Metal Solution Critical
Potential
(V, S.H.E.)
18% Cr, 8% Ni stainless MgCl2, 130°C −0.128

Steel, WQa
MgBr2, 154°C −0.04
steel, cold-rolled 36%
reduction area
steel, WQ
Al, 5.5% Zn, 2.5% Mg 0.5M NaCl, room temperature −1.11
Ti, 7% Al, 2% Cb, 1% Tab 3% NaCl, room temperature −1.1
Mild steel 60% Ca(NO3)2, 3% NH4NO3, 110°C −0.055
63% Cu, 37% Zn brassc 1M (NH4)2SO4, 0.05M CuSO4, pH 6.5, +0.095
room temperature
a
WQ, water-quenched from 1050°C.
b
Precracked specimen.
c
See Fig. 20.7, Section 20.2.3.
Figure 8.6. Effect of applied potential on stress-corrosion cracking of mild steel in 170 g
ammonium carbonate per liter, 70°C [47]. [Reprinted with permission from Corrosion 32 (2),
57 (1976). Copyright NACE International 1976.]
[0.16 V(S.H.E.)] and well removed from the susceptible range, ammonium car-
bonate is not listed among the usually encountered damaging environments.
However, the susceptible potential range may be overlapped under conditions
of cathodic protection accompanied by risk of S.C.C. if carbonates are present.
A similar restricted potential versus time-to-failure curve is exhibited by mild
steel in 35% NaOH at 85–125°C (caustic embrittlement) (Fig. 8.7) [48]. Since the
corrosion potential is at −0.90 V (S.H.E.), S.C.C. does not occur within 200 h or
more unless dissolved O2 or an oxidizing agent, such as PbO, is present that shifts
the corrosion potential into the maximum susceptibility range at or near −0.71 V.
In this event, either anodic or cathodic polarization extends time to failure.
8.3.6 Rate of Crack Growth (Fracture Mechanics)

Under conditions favorable to initiation of S.C.C., the subsequent rate of crack
growth depends on prevailing stress; that is, the higher the stress, the higher the
rate. An empirical linear relation is found between applied stress and log time to
fracture by S.C.C. for smooth specimens of austenitic and martensitic stainless
steels, carbon steels, brass, and aluminum alloys. The linear relation and usually
greater resistance of small-grain-size alloys is shown for brass in Fig. 8.8 [49]. For
some metals, the slope changes to one that is relatively shallow at low values of
stress, indicating greater sensitivity of failure time to change of applied stress. It
will be noted, however, that neither the empirical relation expressing fracture
time versus applied stress nor the typical data of Fig. 8.8 support the concept of
Figure 8.7. Effect of applied potential on failure times of 0.09% C mild steel at three tem-
peratures in 35% sodium hydroxide solution [48]. [Reprinted with permission from Corrosion
28, No. (11), 430 (1972). Copyright NACE International 1972.]
Figure 8.8. Relation of applied stress to time to fracture of 66% Cu, 34% Zn brass exposed
to ammonia. (Data of Morris [49] replotted.)
a threshold stress below which S.C.C. does not occur. A low surface tensile stress
means only that time to fracture is relatively long.
Since stress at a surface is highest at the root of a notch or imperfection, it
is there that a crack grows most rapidly. Surface defects acting as effective stress
raisers include corrosion pits and fatigue cracks. Additionally, at surface defects
that are sufficiently deep, the electrochemical potential differs from that at the
surface; also, the composition and pH of solution within the defect can be altered
by electrochemical transport through operation of differential aeration cells.
These changes plus increased local stress sometimes combine to initiate S.C.C.
as well as accelerate crack growth [50].
The actual stress near the tip of a crack of length a in a stressed elastic solid
can be calculated in terms of the elastic stress intensity factor, K1. For the speci-
men geometry shown in Fig. 8.9, K1 is given by the following expression [51]:
( ) ( ) + ⎤⎥⎦
2
Pa1/ 2 ⎡ a a
K1 = ⎢ 1.99 − 0.41 + 18.70
BW ⎣ W W
where P is applied uniform load, B is specimen thickness, and W is specimen

width. K1 takes into account the load and specimen geometry for a Mode 1 of
crack opening. The dimensions of K1 are ksi in.1/2 or kg mm−3/2. A stress intensity
factor of 20 kg mm−3/2 corresponds to a crack 1 mm deep in a solid subject to a
uniform stress of 10.1 kg/mm2.
If the stress intensity factor K1 is plotted versus a measured S.C.C. crack
velocity, three regions are observed (Fig. 8.10). At low levels of K1, within region
I, crack growth rate is highly sensitive to K1 (unlike region II). A threshold value,
K1S.C.C., is designated at which the measured S.C.C. crack growth rate is very low,
or essentially zero, in short-time tests. From a practical standpoint, the rate cannot
be assumed to be zero unless conditions are such that S.C.C. is not operative. For
reference, a crack growth rate of 10−10 m/s corresponds to 0.1 nm/s, a very low rate
requiring years to measure. In region II, the crack velocity is independent of K1
but is strongly dependent on solution pH, viscosity, and temperature.
Figure 8.9. Mode 1 type of crack opening.

Figure 8.10. Effect of stress intensity at a crack tip on stress-corrosion crack velocity.
Figure 8.11 shows region I and II crack velocities for 7075 Al alloy (1.2–2.0%
Cu, 2.1–2.9% Mg, 0.3% Cr, 5.5% Zn) in NaCl solution and also in liquid mercury
(liquid-metal embrittlement) at room temperature [52]. Crack velocities in
mercury, although orders of magnitude higher than in aqueous solution, show a
similar dependence on stress intensity. Also, metallurgical factors affecting crack
growth rates in one environment are similarly effective in the other. It is reason-
able that some aspects of the crack mechanism overlap in the two different
environments.
For high-strength aluminum alloys, in general, there is no crack growth in
dry air whatever the value of K1. With increase of relative humidity, region I is
shifted to lower stress intensities the higher the humidity, and region II is shifted
to higher velocities [53]. If one assumes that the applied stress is on the order of
the yield strength (Y.S.) of the metal, then a critical crack depth, acr, exists above
which the stress intensity factor exceeds K1S.C.C.. Under this condition, the crack
grows at an increasing rate until failure occurs. Based on the previous expression
for K1, the following approximate relation holds:
2
K1
acr = 0.25⎛ S.C.C. ⎞
⎝ Y.S. ⎠
Figure 8.11. Dependence of crack velocity of 7075 Al alloy on stress intensity factor
K1 [52].
The lower the value of K1S.C.C. and the higher the value of Y.S., the smaller the
allowable depth of surface flaws leading to failure.
8.4 HYDROGEN DAMAGE
Hydrogen damage is a generic term that includes:
• Hydrogen embrittlement (loss of ductility)

• Hydrogen cracking, also called hydrogen stress cracking
• Hydrogen blistering
• Hydrogen-induced cracking (H.I.C.) [also known as stepwise cracking
(S.W.C.) because of its appearance]
• Stress-oriented hydrogen-induced cracking (S.O.H.I.C.)
• Sulfide stress cracking (S.S.C.)
Some metals, when stressed, crack on exposure to a variety of corrosive aqueous

solutions with no evidence that the damaging solutions need be specific. For
example, a stressed high-strength carbon steel or a martensitic stainless steel
HYDROGEN DAMAGE 167
immersed in dilute sulfuric or hydrochloric acid may crack within a few minutes.
The failures have the outward appearance of S.C.C.; but if the alloy is cathodi-
cally polarized, cracking still occurs or happens in shorter time. This is contrary
to the behavior of austenitic stainless steels in boiling magnesium chloride;
such steels are cathodically protected under these conditions. Failures have also
occurred within hours when martensitic 12% Cr-steel self-tapping screws
(cathode) were applied in contact with an aluminum roof (anode) in a moist
atmosphere. Cracking of steel springs, sometimes observed during pickling in
sulfuric acid or after electroplating, is another example. If catalyst poisons that
favor entrance of hydrogen into the metal lattice, such as sulfur or arsenic com-
pounds, are added to the acids, cracking is intensified. When H2S is the poison,
failures are described as sulfide stress cracking (S.S.C.). In practice, many stressed
high-strength steels (e.g., carbon steels or 9% Ni steels) have failed from this
source within days or weeks after exposure to oil-well brines or to natural gas
containing H2S [54].
In all these cases, cracking is caused by hydrogen atoms entering the metal
interstitially either through a corrosion reaction or by cathodic polarization.
Steels containing interstitial hydrogen are not always damaged. They almost
always lose ductility (hydrogen embrittlement), but cracking usually takes place
only under conditions of sufficiently high applied or residual tensile stress. Fail-
ures of this kind are called hydrogen stress cracking or hydrogen cracking. The
cracks tend to be mostly transgranular. In martensite, they may follow former
austenite grain boundaries [55].
Steels are less susceptible to hydrogen cracking above room temperature,
with iron becoming a better catalyst for the reaction Hads + H+ + e− → H2. Hence,
more hydrogen escapes as molecular H2 and less adsorbed H is available to enter
the metal, contrary to the effects of catalyst poisons, which retard the above
reaction.
Carbon steels are especially susceptible to hydrogen cracking when heat-
treated to form martensite, but are less so if the structure is pearlitic. Carbon
steel heat-treated to form a spheroidized carbide structure is less susceptible than
pearlite, bainite, or martensite [56]. Austenitic steels—for example, 18–8 and
14% Mn steel (face-centered cubic), in which hydrogen is more soluble than in
ferrite and the diffusion rate is lower—are immune under most conditions of
exposure [57].
8.4.1 Mechanisms of Hydrogen Damage

The mechanism of hydrogen cracking has been explained by development of
internal pressure [54] on the assumption that interstitial atomic hydrogen is
released as molecular hydrogen at voids or other favored sites under extreme
pressure. Such an effect certainly occurs, as is shown by the formation of visible
blisters containing hydrogen when ductile metals are cathodically polarized or
exposed to certain corrosive media. Under similar conditions, a less ductile metal
would crack instead.
Figure 8.12. Delayed fracture times and minimum stress for cracking of 0.4% C steel as a
function of hydrogen content. Specimen initially charged cathodically, baked at 150°C for
varying times to reduce hydrogen content [59]. [Figure 5 from H. Johnson, J. Morlet, and A.
Troiano, Hydrogen, crack initiation, and delayed failure in steel, Trans. AIME 212, 531
(1958).]
An interesting characteristic of hydrogen cracking is a specific delay time for

appearance of cracks after stress is applied. The delay time is only slightly depen-
dent on stress; it decreases with increasing hydrogen concentration in the steel
and with increase in hardness or tensile strength [58]. For small concentrations
of hydrogen, fracture may occur some days after the stress is applied.
A critical minimum stress exists, below which delayed cracking does not take
place in any time. The critical stress decreases with increase in hydrogen concen-
tration. These effects are shown in Fig. 8.12 for SAE 4340 steel (0.4% C) charged
with hydrogen by cathodic polarization in sulfuric acid, then cadmium-plated to
help retain hydrogen, and finally subjected to a static stress [59]. The hydrogen
concentration was reduced systematically by baking.
Delay in fracture apparently results because of the time required for hydro-
gen to diffuse to specific areas near a crack nucleus until the concentration
reaches a damaging level. These specific areas are presumably arrays of imperfec-
tion sites produced by plastic deformation of metal just ahead of the crack.
Hydrogen atoms preferably occupy such sites because they are then in a lower-
energy state compared to their normal interstitial positions. The crack propagates
discontinuously because plastic deformation occurs first, and then hydrogen dif-
HYDROGEN DAMAGE 169
Figure 8.13 Effect of applied potential on time to failure of 4140 low-alloy steel, Rc46, in
boiling 3% NaCl [60]. (Reproduced with permission. Copyright 1975, The Electrochemical
Society.)
fuses to imperfection arrays produced by deformation, whereupon the crack

propagates one step further. A short notch in a steel surface favors plastic defor-
mation at its base, and hence it lowers the critical minimum stress and shortens
the delay time. Below −110°C or at high deformation speeds, hydrogen embrittle-
ment and cracking are minimized because diffusion of hydrogen is too slow.
It is sometimes assumed that S.C.C. of high-strength steels of hardness >Rc40
(Table 8.1) in water or moist air is caused by hydrogen resulting from the reaction
of H2O with iron. However, the effect of applied potential on failure times shows
that, in boiling 3% NaCl, cracking occurs only above (noble to) a critical potential
of −0.40 ± 0.02 V and below a potential of about −1.1 V (Fig. 8.13) with resistance
to cracking between these potentials. Failure in the upper potential region is
better interpreted as S.C.C., whereas failure at or below −1.1 V corresponds to
hydrogen cracking [60]. In support, steels fail by S.C.C. in H2O above room tem-
perature in shorter times than at room temperature; failure times by hydrogen
cracking (cathodic polarization), to the contrary, are longer the higher the tem-
perature. Also, cold working of high-strength steels improves resistance to S.C.C.
because the critical potential is shifted noble to the corrosion potential, whereas
resistance to hydrogen cracking decreases. Accordingly, in practice, it is important
that high-strength steel bridge cables be cold-drawn in order to avoid failure by
S.C.C. in moist air. In the absence of cold work, they break prematurely despite
more-than-adequate test strength, as has happened in the failure of bridges
in the United States and other countries as well. Furthermore, a surface-

decarburized (hence softer surface) high-strength steel does not fail in boiling
water or 3% NaCl solution, but is readily hydrogen-cracked when cathodically
polarized. The small amount of hydrogen produced by the H2O–Fe reaction has
no effect on the hard steel core. The significant effect of adsorbed H2O rather
than interstitial hydrogen as a cause of cracking of high-strength steels probably
also applies to high-strength martensitic and precipitation-hardening stainless
steels, Al alloys, Mg alloys,Ti alloys, and β and γ brass, all of which are sensitive
to failure in the presence of moisture.
8.4.2 Effect of Metal Flaws

Nuclei for hydrogen cracking of steels form at the interface of precipitated phases
(e.g., Fe3C or intermetallic compounds, such as those occurring in maraging
steels) by separation from the plastically deformed matrix. Nuclei of perhaps
Fe3C in low-carbon 10% Ni–Fe alloys can be oriented by cold rolling, thereby
greatly improving resistance to hydrogen cracking of specimens stressed parallel
to the rolling direction, but not of specimens stressed at right angles [61]. The
role of internal lattice flaws on hydrogen cracking explains in part the resistance
of stressed pure iron to cracking despite its becoming hydrogen-embrittled. On
the other hand, pure carbon–iron alloys crack readily.
In steels, nonmetallic inclusions—for example, MnS—provide internal flaws
where hydrogen blisters often nucleate. The blisters contribute to pipeline fail-
ures by H.I.C. [53], which occurs in three steps:
1. Formation of hydrogen atoms at the steel surface and adsorption on the

surface.
2. Diffusion of hydrogen atoms into the steel substrate.
3. Accumulation of hydrogen atoms at hydrogen traps, such as voids around
inclusions in the steel matrix, leading to increased internal pressure, crack
initiation and propagation, and linkage of separate cracks.
Internal cracks are nucleated where stress intensity is highest, such as at elon-
gated inclusions oriented parallel to the rolling direction; elliptically and spheri-
cally shaped inclusions are less damaging. Eventually, in final failure, cracks
appear at right angles, linking the cracks that previously developed at the elon-
gated inclusions. H.I.C. requires only a steel with a susceptible microstructure
(typically elongated sulfide inclusions) and sufficient hydrogen to cause cracking.
H.I.C. can occur in the absence of any applied or residual stress in the steel other
than the hydrogen pressure in traps.
Under the influence of an applied stress, failure can occur by S.O.H.I.C.,
similar to H.I.C. except that the morphology of cracking is different. Whereas in
H.I.C. the blister cracks form at widely distributed sites and then link in a step-
wise pattern, in S.O.H.I.C. the blister cracks tend to form in an array that is per-
HYDROGEN DAMAGE 171
2 mm
(a)
(b)
Figure 8.14. (a) Hydrogen-induced cracking (H.I.C.). (b) Stress-oriented hydrogen-induced

cracking (S.O.H.I.C.). (Courtesy of Malcolm Hay.)
pendicular to the applied stress, and these individual blister cracks link leading
to failure. Figure 8.14 presents illustrations of H.I.C. and S.O.H.I.C.
Any factors that reduce hydrogen absorption in the corrosion process are
beneficial; for example, alloying with a small percentage of Pt or Pd, which cata-
lyze formation of molecular hydrogen at the steel surface [62], or with copper,
which forms an insoluble sulfide film that provides some protection at pH above
about 4.5. Similarly, any processing of steel that minimizes sharp internal surfaces
at the inclusion interface, for example by avoiding low rolling temperatures,
reduces the tendency toward cracking. Increased resistance to H.I.C. can also be
obtained by reducing the sulfur content in the steel and by controlling the shape
of sulfides—for example, by adding calcium to the steel composition.
Surface flaws may influence the hydrogen cracking (or sulfide cracking) of
moderate- or high-strength steels exposed to oil-well brines containing H2S.
Marked susceptibility to cracking in this environment makes it necessary to
specify steels below the strength level at which failure occurs. Strength of a steel
is proportional to its hardness. The empirically determined maximum hardness
is specified as Rockwell C 22 (Rc22), corresponding to a yield strength of about
90 ksi [63]. It has been suggested [64], based on threshold values of stress intensity
factors for steels exposed to aqueous H2S solutions, that Rc22 corresponds to a
critical surface-flaw depth of about 0.5 mm (0.02 in). At greater depths, flaws are
likely to develop quickly into major cracks. Small-size flaws of this order, which
are calculated to be still less tolerable for harder steels, are not readily avoided
in practice, corresponding with the general experience of the oil industry that, in
H2S environments, steels of hardness >Rc22 should be avoided. In general, surface
flaws become more important to cracking the higher the strength of the steel;
internal flaws, on the other hand, affect both low- and high-strength steels.
8.5 RADIATION DAMAGE
Radiation damage is the change of properties of a material caused by exposure

to ionizing radiation, such as X-rays, gamma rays, neutrons, heavy-particle radia-
tion, or fission fragments in nuclear fuel material [65]. Metals exposed to intense
radiation in the form of neutrons or other energetic particles undergo lattice
changes resembling in many respects those produced by severe cold work. The
porous structure produced by dealloying has been described as similar to that
found in irradiated materials [66]. Lattice vacancies, interstitial atoms, and dislo-
cations are produced, and these increase the diffusion rate of specific impurities
or alloyed components. In copper and nickel at room temperature, radiation
damage leads to increased hardness, caused by clusters of interstitials and vacan-
cies [66]. During radiation, a local temperature rise, called “temperature spike,”
may occur. There are two kinds of spikes: thermal spikes, in which few or no atoms
leave their lattice sites, and displacement spikes, in which many atoms move into
interstitial positions.
Except for chemicals produced in the environment by radiation, such as
HNO3 and H2O2, which have a secondary effect on corrosion, or formation of
localized displacement spikes during radiation, the effect of radiation may be
expected to parallel that of cold work. That is, metals for which the corrosion rate
is controlled by oxygen diffusion should suffer no marked change in rate after
irradiation. In acids, on the other hand, irradiated steel (but not pure iron) would
presumably have a greater increase in rate than would irradiated nickel, which
is less sensitive to cold working.
Austenitic stainless steels often become more sensitive to S.C.C. after cold
working; on this basis, they might be expected to become more sensitive after
irradiation. Indeed, irradiation-assisted stress-corrosion cracking (I.A.S.C.C.) is a
cause of failure of core components in both boiling water reactors (BWR) and
pressurized water reactors (PWR), and it has been observed, as intergranular
S.C.C., in austenitic stainless steels and nickel-base alloys [67]. The complexities
of S.C.C. are, in I.A.S.C.C., compounded by the effects of radiation on microstruc-
ture, microchemistry, and deformation behavior of the material as well as on the
chemistry and electrochemistry of the solution. I.A.S.C.C. of austenitic stainless
steels is related to chromium depletion along grain boundaries. In addition to the
grain-boundary chromium depletion that can result from sensitization during
CORROSION FATIGUE 173
welding (see Figs. 19.2 and Fig. 19.3, Section 19.2.3.1), chromium depletion in the
grain boundary can also occur because of neutron irradiation, further reducing
resistance to S.C.C. [68, 69]. One materials solution to mitigate I.G.S.C.C. in
nuclear reactors is to use nuclear-grade stainless steels, such as type 316NG and
type 304NG, which have a maximum carbon content of 0.020% and a nitrogen
content of 0.060 to 0.100% to maintain strength at the lower carbon content
compared to the non-nuclear grades (see Table 19.2, Section 19.2.2) [69]. Niobium-
stabilized, type 347 stainless steel, with low carbon called 347NG, has also been
used successfully [70]. Of course, good corrosion design is also essential—for
example, a design without crevices, which can provide sites for localized corrosion
(see Sections 2.3 and 19.2.).
The effect of irradiation on corrosion of some uranium alloys is consider-
able. For example, a 3% Cb–U alloy having moderate resistance to water at
260°C disintegrated within 1 h after irradiation. Furthermore, the corrosion of a
zirconium alloy (Zircaloy-2, see Section 26.2) at 250°C in dilute uranyl sulfate
solution containing small amounts of H2SO4 and CuSO4 was very much increased
by reactor irradiation [71]. In a review of the subject, Cox [72] stated that both
fast neutron irradiation and presence of dissolved oxygen or an oxidizing elec-
trolyte must be present simultaneously for any observed acceleration of corro-
sion to occur in high-temperature water. Accelerated corrosion of Zircaloys
induced by irradiation is not observed above 400°C (750°F). The effects have
been explained in terms of changes in the physical properties of the protective
oxide film.
8.6 CORROSION FATIGUE
A metal that progressively cracks on being stressed alternately (reverse bending)

or repeatedly is said to fail by fatigue. The greater the applied stress at each cycle,
the shorter is the time to failure. A plot of stress versus number of cycles to failure,
called the S–N curve, is shown in Fig. 8.15. A number of cycles at the correspond-
ing stress to the right of the upper solid line results in failure, but no failure occurs
for an infinite number of cycles at or below the endurance limit or fatigue limit.
For steels, but not necessarily for other metals, a true endurance limit exists which
is approximately half the tensile strength. The fatigue strength of any metal, on
the other hand, is the stress below which failure does not occur within a stated
number of cycles. Frequency of stress application is sometimes also stated because
this factor may influence the number of cycles to failure.
In general, a corrosive environment can decrease the fatigue properties of
any engineering alloy, meaning that corrosion fatigue is not dependent on mate-
rial and environment [73]. In a corrosive environment, failure at a given stress
level usually occurs within fewer cycles, and a true fatigue limit is not observed
(Fig. 8.15). In other words, failure occurs at any applied stress if the number of
cycles is sufficiently large. Cracking of a metal resulting from the combined action
of a corrosive environment and repeated or alternate stress is called corrosion
Figure 8.15. S–N curve for steels subjected to cyclic stress.
Figure 8.16. Corrosion-fatigue crack through mild steel sheet, resulting from fluttering of
the sheet in a flue gas condensate (250×).
fatigue. The damage is almost always greater than the sum of the damage by cor-
rosion and fatigue acting separately.
Corrosion-fatigue cracks are typically transgranular. They are often branched
(Fig. 8.16), and several cracks are usually observed at the metal surface in the
vicinity of the major crack accounting for failure. Fatigue cracks are similarly
transgranular (exception: lead and tin), but rarely is there evidence of more than
one major crack. In corrosion fatigue, corrosion pits may form at the metal
surface at the base of which cracks initiate, but pitting is not a necessary precur-
sor to failure.
Aqueous environments causing corrosion fatigue are numerous and are not
specific, contrary to the situation for S.C.C., for which only certain ion–metal
combinations result in damage. Corrosion fatigue of steel occurs in fresh waters,
seawater, combustion-product condensates, general chemical environments, and
so on, with the general rule that the higher the uniform corrosion rate, the shorter
the resultant fatigue life.
Corrosion fatigue is a common cause of unexpected cracking of vibrating
metal structures designed to operate safely in air at stresses below the fatigue
limit. For example, the shaft of a ship propeller slightly out of line will operate
satisfactorily until a leak develops, allowing water to impinge on the shaft in the
area of maximum alternating stress. Cracks may then develop within a matter of
days, resulting in eventual parting and failure of the shaft. Steel oil-well sucker
rods, used to pump oil from underground, have limited life because of corrosion
fatigue resulting from exposure to oil-well brines. Despite use of high-strength
medium-alloy steels and oversized rods, failures from this source are a loss to the
oil industry in the order of millions of dollars annually. Wire cables commonly
fail by corrosion fatigue. Pipes carrying steam or hot liquids of variable tempera-
ture may fail similarly because of periodic expansion and contraction (thermal
cycling).
The usual fatigue test conducted in air on a structural metal is influenced by
both oxygen and moisture and, in part, therefore, always represents a measure
of corrosion fatigue. In early tests, the fatigue strength for copper in a partial
vacuum was found to be increased 14% over that in air. For mild steel the
increase was only 5%, but for 70–30 brass it was 26% [74]. In later tests [75],
fatigue life of oxygen-free, high-conductivity (OFHC) copper at 10−5 mmHg air
pressure was found to be 20 times greater than at 1-atm air pressure. The main
effect was attributed to oxygen; this had little effect on initiation of cracks, but
had considerable effect on rate of crack propagation. Fatigue life of pure alumi-
num was also affected by air; but contrary to the situation for copper, water vapor
in absence of air was equally effective. Gold, which neither chemisorbs oxygen
nor oxidizes, had the same life whether fatigued in air or in a vacuum.
In some environments, fatigue cracking is supplemented by S.C.C., with the
latter occurring under conditions of constant stress. This is seen in the behavior
of a high-strengh low-alloy steel fatigued in both the absence and presence of
moisture. Steels of greater than about 1140 MPa (165 ksi) yield strength (Rc37)
are subject to S.C.C. in water at room temperature and have shorter fatigue life
in moist air compared to dry air; whereas steels of lower strength, which do not
undergo S.C.C. in water, have the same fatigue life (Fig. 8.17) [76].
Fresh waters and particularly brackish waters have a greater effect on the
corrosion fatigue of steels than on that of copper, with the latter being a more
corrosion-resistant metal. Stainless steels and nickel or nickel-base alloys are also
better than carbon steels. In general, resistance of a metal to corrosion fatigue is
Figure 8.17. Tensile strength, yield strength, fatigue limit in dry air, and fatigue strength at
107 cycles in 93% relative humidity air, of 4140 steel heat-treated to various hardness values
[76]. (With kind permission of Springer Science and Business Media.)
associated more nearly with its inherent corrosion resistance than with high
mechanical strength.
A few values of corrosion fatigue strength determined by McAdam [77] in
fresh and brackish waters are listed in Table 8.5. These values, besides varying
with environment, are found to vary with rate of stressing, with temperature,
and with aeration; hence, they are useful only for qualitative comparison of
one metal with another. Unlike the fatigue limit in air, they are not usually reli-
able for engineering design. Conclusions from data of Table 8.5 and similar data
are as follows:
1. There is no relation between corrosion fatigue strength and tensile

strength.
2. Medium-alloy steels have only slightly higher corrosion fatigue strength
than carbon steels.
TABLE 8.5. Fatigue Limit and Corrosion Fatigue Strength of Various Metals [77]
Metal Fatigue Corrosion Damage Ratio
Limit Fatigue Strength (Corrosion
in Air (psia) Fatigue
(psia) Strength)/
(Fatigue
Limit)
Well Salt Well Salt

Waterb Waterc Water Water
(107–108 cycles at 1450 cycles/min)

0.11% C steel, annealed 25,000 16,000 0.64
0.16% C steel, quenched and tempered 35,000 20,000 7,000 0.57 0.2
1.09% C steel, annealed 42,000 23,000 0.55
3.5% Ni, 0.3% C steel, annealed 49,000 29,000 0.59
0.9% Cr, 0.1% V, 0.5% C steel, annealed 42,000 22,000 0.52
13.8% Cr, 0.1% C steel, quenched and 50,000 35,000 18,000 0.70 0.36
tempered
17% Cr, 8% Ni, 0.2% C steel, hot-rolled 50,000 50,000 25,000 1.00 0.50
Nickel, 98.96%, annealed 760°C 33,000 23,500 21,500 0.71 0.65
Monel, 67.5% Ni, 29.5% Cu, annealed 36,500 26,000 28,000 0.71 0.77
760°C
Cupro-nickel, 21% Ni, 78% Cu, annealed 19,000 18,000 18,000 0.95 0.95
760°C
Copper, annealed 650°C 9,800 10,000 10,000 1.02 1.02
Aluminum, 99.4%, annealed 5,900 2,100 0.36
Aluminum, 98%, 1.2% Mn, hard 10,700 5,500 3,800 0.51 0.36
Duralumin, tempered 17,000 7,700 6,500 0.45 0.38
Brass, 60–40, annealed 21,000 18,000 0.86
a
To convert from psi to MPa, multiply by 6890.
b
2 ppm CaSO4, 200 ppm CaCO3, 17 ppm MgCl2, 140 ppm NaCl.
c
Severn River water, with about one-sixth the salinity of seawater.
3. Heat treatment does not improve corrosion fatigue strength of either

carbon or medium-alloy steels; residual stresses are deleterious.
4. Corrosion-resistant steels, particularly steels containing chromium, have
higher corrosion fatigue strength than other steels.
5. Corrosion fatigue strength of all steels is lower in salt water than in fresh
water.
8.6.1 Critical Minimum Corrosion Rates

In order for the corrosion process to affect fatigue life, the corrosion rate must
exceed a minimum value. Such rates are conveniently determined by anodic
polarization of test specimens in deaerated 3% NaCl, translating uniform
TABLE 8.6. Critical Minimum Corrosion Rates, 25°C,

30 Cycles/s
i Reference
μA/cm2 a gmd
0.18% C mild steel 2.0 0.50 78

4140 low alloy steel
Rc20 2.5 0.63 76
Rc37 2.0 0.50 76
Rc44 2.8 0.70 76
Nickel 1.2 <0.30 79
OFHC copper 100 28.5 80
a
To convert μA/cm2 to A/m2, divide by 100.
current densities by Faraday’s Law into corrosion rates below which the fatigue
life is unaffected. These measured current densities are found to be indepen-
dent of the total area of specimen surface exposed to anodic currents. Various
values at 30 cycles/s (1800 cycles/min) are listed in Table 8.6. It is expected that
such values increase with cyclic frequency of the test. For the steels, critical
corrosion rates are independent of (a) carbon content, (b) applied stress below
the fatigue limit, and (c) heat treatment (hardness). The average value of
0.58 gmd (5.8 mdd) is less than the uniform corrosion rates of steels in aerated
water and 3% NaCl (1–10 gmd, 10–100 mdd). But at pH 12, the uniform corro-
sion rate falls below the critical rate, and the fatigue life regains its value in air
[78]. The existence of a critical rate in 3% NaCl explains why cathodic protec-
tion of steel against corrosion fatigue requires polarizing to only −0.49 V
(S.H.E.), whereas the value required to attain zero corrosion rate lies 40 mV
more active at −0.53 V.
For copper, the critical rate of 28.5 gmd (285 mdd) is much higher than the
uniform corrosion rates in aerated water and 3% NaCl (0.4–1.5 gmd, 4–15 mdd);
hence, the fatigue life of copper is observed to be about the same in air as in
fresh and saline waters (Table 8.5).
8.6.2 Remedial Measures

There are several means available for reducing corrosion fatigue. In the case of
mild steel, thorough deaeration of a saline solution restores the normal fatigue
limit in air (Fig. 8.18) [81]. Cathodic protection to −0.49 V (S.H.E.) accomplishes
the same result. Inhibitors are also effective [82, 83]. Sacrificial coatings (e.g., zinc
or cadmium electrodeposited on steel) are effective because they cathodically
protect the base metal at defects in the coating. One of the very first observations
and diagnoses of corrosion fatigue, made by B. Haigh in about 1916, involved
premature failure of steel towing cables exposed to seawater, and galvanizing
Figure 8.18. Effect of dissolved oxygen concentration in 3% NaCl, 25°C, on fatigue behavior
of 0.18% C steel [81]. (Reprinted with permission of ASM International®. All rights reserved.
www.asminternational.org.)
provided greatly increase life in this application [84]. Electrodeposits of tin, lead,
copper, or silver on steel are also said to be effective without reducing normal
fatigue properties; presumably, they owe their effectiveness to exclusion of the
environment [85]. Organic coatings are useful if they contain inhibiting pigments
in the prime coat. Shot peening the metal surface, or otherwise introducing com-
pressive stresses, is beneficial.
8.6.3 Mechanism of Corrosion Fatigue

The mechanism of fatigue in air proceeds by localized slip within grains of the
metal caused by alternating stress, resulting in slip steps at the metal surface.
Adsorption of air on the clean metal surface exposed at slip steps probably pre-
vents rewelding on the reverse stress cycle. Continued slip produces displaced
clusters of slip bands, which protrude above the metal surface (extrusions); cor-
responding incipient cracks (intrusions) form elsewhere (Fig. 8.19). Below the
fatigue limit, work hardening accompanying each cycle of plastic deformation
eventually impedes further slip, which in turn impedes the fatigue process.
The basic effect of the corrosion process is to accelerate plastic deformation
accompanied by formation of extrusions and intrusions. For this reason, damage
by corrosion fatigue—a conjoint action of corrosion and fatigue—is greater than
the damage caused by the sum of both acting separately. In addition, corrosion
resistance of a metal is usually more important than high tensile strength in
Figure 8.19. Extrusions and intrusions in copper after 6 × 105 cycles in air. Specimen plated
with silver after test and mounted at an angle to magnify surface protuberances by about
20×. Overall magnification about 500×. [Figure 3 from W. Wood and H. Bendler, The fatigue
process in copper as studied by electron metallography, Trans. Metall. Soc. AIME 224, 182
(1962).]
establishing optimum resistance to corrosion fatigue. Since pure metals are not
immune to uniform corrosion, they are also not immune to corrosion fatigue.
The mechanism of the slip dissolution process [86] takes place in the follow-
ing steps:
• Diffusion of the active species to the crack tip

• Rupture of the protective film at the slip step
• Dissolution of the exposed surface
• Nucleation and growth of the protective film on the bare surface
8.7 FRETTING CORROSION
Fretting corrosion is another phenomenon that occurs because of mechanical

stresses, and, in the extreme, it may lead to failure by fatigue or corrosion fatigue.
FRET TING CORROSION 181
Figure 8.20. Weight loss of mild steel versus mild steel by fretting corrosion in air [87].
It is defined as damage occurring at the interface of two contacting surfaces, one

or both being metal, subject to slight relative slip. The slip is usually oscillatory
as, for example, that caused by vibration. Continuous slip, as when one roll moves
slightly faster than another roll in contact, leads to similar damage. Wear corro-
sion and friction oxidation are terms that have also been applied to this kind of
damage.
Damage by fretting corrosion is characterized by discoloration of the metal
surface and, in the case of oscillatory motion, by formation of pits. It is at such
pits that fatigue cracks eventually nucleate. The rapid conversion of metal to
metal oxide may, in itself, cause malfunction of machines, because dimensional
accuracy is lost, or corrosion products may cause clogging or seizing. The corro-
sion products are exuded from the faying surfaces, which, in the case of steel, are
largely composed of αFe2O3 plus a small amount of iron powder [87]. In the case
of nickel for continuous-slip experiments, the products are NiO and a small
amount of nickel; for copper, they are Cu2O with lesser amounts of CuO and
copper [88].
Fretting corrosion is frequently the cause of failure of suspension springs,
bolt and rivet heads, king pins of auto steering mechanisms, jewel bearings,
variable-pitch propellers, shrink fits, contacts of electrical relays, connecting rods,
and many parts of vibrating machinery. It may cause discoloration of stacked
metal sheets during shipment. One of the first examples of fretting corrosion was
recognized when automobiles were shipped some years ago by railroad from
Detroit to the West Coast. Because of vibration, the ball-bearing races of the
wheels became badly pitted by fretting corrosion, so that the automobiles were
not operable. Damage was worse in winter than in summer, but could be avoided
if the load on the wheels was relieved during shipment.
Fretting corrosion occurs on airframe structural surfaces that move against
each other in a corrosive environment. High vibration levels and other types of
mechanical stress result in small relative movement between parts of operational
aircraft systems [89]. Another example of fretting corrosion can occur with rail-
road car wheels that are shrink-fitted onto their axles. If failure occurs causing
the wheel to come off the axle, it can cause derailment and other damage [90].
Electrical contacts made of electroplated gold coatings can fail by fretting cor-
rosion. Relative motion between the contacts removes the gold plate, and atmo-
spheric corrosion of the substrate increases the contact resistance to intolerable
levels [91]. Fretting corrosion is also a problem in nuclear reactors, particularly
on heat-exchanger tubes and on fuel elements, where fluid flow generates vibra-
tions [92].
Laboratory experiments [87] have shown that fretting corrosion of steel
versus steel requires oxygen, but not moisture. Also, damage is less in moist air
compared to dry air and is much less in a nitrogen atmosphere. Damage increases
as temperature is lowered. The mechanism, therefore, is obviously not electro-
chemical. Increased load increases damage, accounting for the tendency of pits
to develop at contacting surfaces because corrosion products—for example,
αFe2O3—occupy more volume (2.2 times as much in the case of iron) than the
metal from which the oxide forms. Because the oxides are unable to escape
during oscillatory slip, their accumulation increases the stress locally, thereby
accelerating damage at specific areas of oxide formation. Fretting corrosion is
also increased by increased slip, provided that the surface is not lubricated.
Increase in frequency for the same number of cycles decreases damage, but in
nitrogen no frequency effect is observed. These effects are depicted in Fig. 8.20.
Note that the initial rate of metal loss during the run-in period is greater than
the steady-state rate.
8.7.1 Mechanism of Fretting Corrosion

When two surfaces touch, contact occurs only at relatively few sites, called asperi-
ties, where the surface protudes. Relative slip of the surfaces causes asperities to
FRET TING CORROSION 183
rub a clean track on the opposite surface, which, in the case of metal, immediately
becomes covered with adsorbed gas, or it may oxidize superficially. The next
asperity wipes off the oxide; or it may mechanically activate a reaction of adsorbed
oxygen with metal to form oxide, which in turn is wiped off, forming another
fresh metal track (Fig. 8.21). This is the chemical factor of fretting damage. In
addition, asperities plow into the surface, causing a certain amount of wear by
welding or shearing action, through which metal particles are dislodged. This is
the mechanical factor. Any metal particles eventually are converted partially into
oxide by secondary fretting action of particles rubbing against themselves or
against adjacent surfaces. Also, the metal surface after an initial run-in period is
fretted by oxide particles moving relative to the metal surface rather than by the
mating opposite surface originally in contact (hence, electrical resistance between
the surfaces is at first low, then becomes high and remains so).
An equation for weight loss W of a metal surface undergoing fretting corro-
sion by oscillatory motion has been derived [93] (Appendix, Section 29.7) on the
basis of the model just described, which accounts reasonably satisfactorily for
data of Fig. 8.20:
C
W = (k0 L1/ 2 − k1L) + k2 lLC
f
where L is the load, C is the number of cycles, f is the frequency, l is the slip, and
k0, k1, and k2 are constants. The first two terms of the right-hand side of the equa-
tion represent the chemical factor of fretting corrosion. These become smaller
the higher the frequency, f, corresponding to less available time for chemical
reaction (or adsorption) per cycle. The last term is the mechanical factor inde-
pendent of frequency, but proportional to slip and load. It is found that either
the mechanical or chemical factor may dominate in accounting for damage
depending on specific experimental conditions. In nitrogen, the mechanical factor
alone is operable, the debris is metallic iron powder, and W is independent of
frequency, f.
Fretting corrosion is not a high-temperature oxidation phenomenon. This
is demonstrated by increased damage at below-room temperatures; by less
Figure 8.21. Idealized model of fretting action at a metallic surface.

damage at high frequencies, for which surface temperatures are highest; by the
fact that oxide produced in fretting corrosion of iron is αFe2O3 and not the high-
temperature form, Fe3O4; and, finally, by steel being badly fretted in contact with
polymethacrylate plastic, which melts at 80°C, and hence the surface could have
reached temperatures of this order, but not higher [94].
The effect of moisture when adsorbed on the metal surface may be that
of a lubricant. In addition, hydrated αFe2O3 is probably less abrasive than the
anhydrous oxide. At low temperatures, damage is greater presumably because O2
can adsorb more rapidly or more completely than at high temperatures. More
fundamental research is needed to help clarify these details of the general
mechanism.
8.7.2 Remedial Measures

1. Combination of a Soft Metal with a Hard Metal. At sufficiently high loads,
soft metals serve to exclude air at the interface; furthermore, a soft metal
may yield by shearing instead of sliding at the interface, thereby reducing
damage. Tin-, silver-, lead- indium-, and cadmium-coated metals in contact
with steel have been recommended. Brass in contact with steel tends to
be less damaging than steel versus steel. Combinations of stainless steels
tend to be worst.
2. Design of Contacting Surfaces to Avoid Slip Completely (e.g., grit blasting,
or otherwise roughening the surface). Intentional design to completely
avoid slip is not always easy to accomplish, because damage is presumably
caused by relative movement approaching the order of atomic dimensions.
Increased load is effective in this direction if it is high enough to prevent
slip; otherwise, damage is worse.
3. Application of Cements (e.g., rubber cement to the faying surfaces).
Cements exclude air from the interface.
4. Use of Lubricants. Low-viscosity oils, particularly in combination with a
phosphate-treated surface, can be helpful in reducing damage if the load
is not too high. Low-viscosity oils diffuse more readily to the clean metal
surface produced by oscillatory slip. Molybdenum sulfide is effective as a
solid lubricant, particularly if baked onto the surface, but the beneficial
effects tend to be temporary because the lubricant is eventually displaced
by surface movement.
5. Use of Elastomer Gaskets or Materials of Low Coefficient of Friction.
Rubber absorbs motion, thereby avoiding slip at the interface. Polytetra-
fluoroethylene (Teflon) has a low coefficient of friction and reduces
damage. Because of their relatively poor strength, materials of this kind
are expected to be effective only at moderate loads.
6. Use of Cobalt-base Alloys. These are effective especially in the presence
of liquid water or aqueous solutions (see Chapter 24).
REFERENCES 185
REFERENCES

2. H. Copson, in Corrosion Handbook, H. H. Uhlig, editor, Wiley, New York, 1948,
p. 577.
3. E. A. Charles and R. N. Parkins, Corrosion 51(7), 518 (1995).
4. W. Schroeder and A. Berk, Intercrystalline Cracking of Boiler Steel and Its Prevention,
Bureau of Mines Bulletin 443, U.S. GPO, Washington, D.C., 1941.
5. R. Parkins, in Stress Corrosion Cracking and Embrittlement, W. Robertson, editor,
Wiley, New York, 1956, p. 154.
6. M. A. Streicher, in Uhlig’s Corrosion Handbook, 2nd edition, R. W. Revie, editor, Wiley,
New York, 2000, pp. 1247–1248.
7. M. Holzworth et al., Mater. Prot. 7(1), 36 (1968).
8. R. Pollard, in Symposium on Stress-Corrosion Cracking of Metals, ASTM–AIME,
Philadelphia, PA, 1944, p. 437.
9. D. A. Jones, C. D. Kim, and B. E. Wilde, Corrosion 33(2), 50 (1977).
10. R. Treseder and A. Wachter, Corrosion 5, 383 (1949).
11. M. Kowaka and S. Nagata, Corrosion 24, 427 (1968); A Brown, J. Harrison, and R. Wilkins,
Corros. Sci. 10, 547 (1970).
12. H. Buchholtz and R. Pusch, Stahl u. Eisen 62, 21 (1942).
13. R. N. Parkins, in Uhlig’s Corrosion Handbook, 2nd edition, R. W. Revie, editor, Wiley,
New York, 2000, pp. 191–194.
14. National Energy Board of Canada, Public Inquiry Concerning Stress Corrosion Crack-
ing on Canadian Oil and Gas Pipelines, Report of the Inquiry, MH-2–95, National
Energy Board, Calgary, Alberta, Canada, November 1996.
15. H. H. Uhlig and J. Sava, Trans. Am. Soc. Metals 56, 361 (1963).
16. M. Long and H. Uhlig, J. Electrochem. Soc. 112, 964 (1965).
17. R. N. Parkins, J. Iron Steel Inst. 172, 149 (1952).
18. K. Bohnenkamp, in Proceedings, Conference Fundamental Aspects of Stress Corrosion
Cracking, National Association of Corrosion Engineers, Houston, TX, 1969, p. 374.
19. E. Baerlecken and W. Hirsch, Stahl u. Eisen 73, 785 (1953).
20. H. Uhlig, K. Elayaperumal, and M. Talerman, Corrosion 30, 229 (1974).
21. V. Agarwala, M. S. thesis, Department of Metallurgy and Materials Science, M.I.T.,
Cambridge, MA, 1966.
New York, 2000, p. 200.
23. W. Lynes, Corrosion 21, 125 (1965).
24. M. Scheil, in Symposium on Stress-Corrosion Cracking of Metals, ASTM–AIME,
Philadelphia, PA, 1945, p. 433.
25. K. Sieradski and R. C. Newman, Philos. Mag. A 51 (1), 95 (1985).
26. T. Magnin, A. Chambreuil-Paret, J. P. Château, D. Delafosse, and B. Bayle, in Corrosion–
Deformation Interactions, European Federation of Corrosion Publications, No. 21, The
Institute of Materials, London, 1997, p. 12.
27. H. Uhlig and E. Cook, Jr., J. Electrochem. Soc. 116, 173 (1969).
28. T. Beck and M. Blackburn, Am. Inst. Aeronaut. Astronaut. J. 6, 326 (1968).
29. E. Dix, Min. Metall. Eng. 137, 11 (1940).
30. S. P. Pednekar, A. K. Agrawal, H. E. Chaung, and R. W. Staehle, J. Electrochem. Soc. 126,
701 (1979).
31. R. N. Parkins, Stress corrosion cracking, in Environment-Induced Cracking of Metals,
Proceedings of the First International Conference on Environment-Induced Cracking
of Metals, October 1988, R. P. Gangloff and M. B. Ives, editors, National Association
of Corrosion Engineers, Houston, TX, 1990, p. 10.
32. I.-H. Lin and R. M. Thomson, J. Mater. Res. 1, 1 (1986).
33. G. J. Dienes, K. Sieradzki, A. Paskin, and B. Massoumzadeh, Surf. Sci. 144, 273 (1984).
34. R. H. Jones, in ASM Handbook, Vol. 13A, Corrosion: Fundamentals, Testing, and Pro-
tection, ASM International, Materials Park, OH, 2003, p. 362.
35. S. P. Lynch, Hydrogen Effects in Metals, A. W. Thompson and I. M. Bernstein, editors,
The Metallurgical Society, 1981, p. 863.
36. S. P. Lynch, Met. Sci. 15 (10), 463 (1981).
37. S. P. Lynch, J. Mater. Sci. 20, 3329 (1985); see also S. P. Lynch, in Corrosion–Deformation
Interactions, CDI ’96, Second International Conference on Corrosion–Deformation
Interactions in Conjunction with EUROCORR ’96, European Federation of Corrosion
Publications, Number 21, The Institute of Metals, London, 1997, p. 206.
38. H. H. Uhlig, in Physical Metallurgy of Stress Corrosion Fracture, T. Rhodin, editor,
Interscience, New York, 1959, pp. 1–17.
39. E. Coleman, D. Weinstein, and W. Rostoker, Acta Metall. 9, 491 (1961).
40. A. Griffith, Philos. Trans. A220, 163 (1920).
41. R. Mears, R. Brown, and E. Dix, Jr., in Symposium on Stress-Corrosion Cracking of
Metals, ASTM–AIME, Philadelphia, 1945, p. 323.
42. F. Fischer, Kunststoffe 55, 453 (1965).
43. N. Petch and P. Stables, Nature 169, 842 (1952).
44. W. Rostoker, J. M. McCaughey, and H. Markus, Embrittlement by Liquid Metals,
Reinhold, New York, 1960.
45. H. Uhlig, J. Appl. Electrochem. (Gr. Britain) 9, 191 (1979).
46. R. Newberg and H. Uhlig, J. Electrochem. Soc. 120, 1629 (1973).
47. D. Hixson and H. Uhlig, Corrosion 32, 56 (1976).
48. H. Mazille and H. Uhlig, Corrosion 28, 427 (1972).
49. A. Morris, Trans. Am. Inst. Min. Metall. Eng. 89, 256 (1930).
50. M. Elboujdaini, Y.-Z. Wang, R. W. Revie, R. N. Parkins, and M. T. Shehata, Stress corrosion
crack initiation processes: Pitting and microcrack coalescence, Paper No. 00379,
CORROSION/2000, NACE International, Houston, TX, 2000.
51. D. Broek, Elementary Engineering Fracture Mechanics, 4th revised edition, Kluwer
Academic Publishers, The Netherlands, 1986, p. 85.
52. M. Speidel, in Theory of Stress Corrosion Cracking in Alloys, J. Scully, editor, North
Atlantic Treaty Organization, Scientific Affairs Division, Brussels, 1971, pp. 298 and
302.
53. ibid, p. 305.
54. M. Elboujdaini, Hydrogen-induced cracking and sulfide stress cracking, in Uhlig’s Cor-
rosion Handbook, 2nd edition, R. W. Revie, editor, Wiley, New York, 2000, pp. 205–220.
REFERENCES 187
55. A. Schuetz and W. Robertson, Corrosion 13, 437t (1957).

56. P. Bastien, in Physical Metallurgy of Stress Corrosion Fracture, T. Rhodin, editor, Inter-
science, New York, 1959, p. 311.
57. H. H. Uhlig, Trans. Am. Inst. Min. Metall. Eng. 158, 183 (1944).
58. A. Troiano, Trans. Am. Soc. Metals 52, 54 (1960).
59. H. Johnson, J. Morlet, and A. Troiano, Trans. Am. Inst. Min. Metall. Eng. 212, 528 (1958).
60. A. Asphahani and H. Uhlig, J. Electrochem. Soc. 122, 174 (1975).
61. J. Marquez, I. Matsushima, and H. Uhlig, Corrosion 26, 215 (1970).
62. B. Wilde, C. Kim, and E. Phelps, Corrosion 36, 625 (1980).
63. NACE Committee T-1F, Materials Performance 12(3), 41 (1973).
64. C. Carter and M. Hyatt, in Stress Corrosion Cracking and Hydrogen Embrittlement of
Iron-Base Alloys, R. Staehle et al., editor, National Association of Corrosion Engi-
neers, Houston, TX, 1977, p. 551.
65. ASM Handbook, Vol. 13A, Corrosion: Fundamentals, Testing, and Protection, ASM
International, Materials Park, OH, 2003, p. 1023.
66. R. H. Jones, in Environment-Induced Cracking of Metals, Proceedings of the First
International Conference on Environment-Induced Cracking of Metals, October 1988,
R. P. Gangloff and M. B. Ives, editors, National Association of Corrosion Engineers,
Houston, TX, 1990, p. 284.
67. R. H. Jones and S. M. Bruemmer, Environment-induced crack growth processes in
nickel-base alloys, in Environment-Induced Cracking of Metals, Proceedings of the
First International Conference on Environment-Induced Cracking of Metals, October
1988, R. P. Gangloff and M. B. Ives, editors, National Association of Corrosion Engi-
neers, Houston, TX, 1990, pp. 289–290; G. S. Was and P. L. Andresen, Stress corrosion
cracking behavior of alloys in aggressive nuclear reactor core environments, Corrosion
63 (1), 19 (2007).
68. F. P. Ford, B. M. Gordon, and R. M. Horn, Corrosion in boiling water reactors, in ASM
Handbook, Vol. 13C, Corrosion: Environments and Industries, ASM International,
Materials Park, OH, 2006, p. 347.
69. G. S. Was, J. Busby, and P. L. Andresen, Effect of irradiation on stress-corrosion cracking
and corrosion in light water reactors, in ASM Handbook, Vol. 13C, Corrosion: Envi-
ronments and Industries, ASM International, Materials Park, OH, 2006, pp. 386–404.
70. Ref. 68, p. 354.
71. M. Simnad, in The Effects of Radiation on Materials, J. J. Harwood et al., editors,
Reinhold, New York, 1958, pp. 129–133.
72. D. Cox, J. Nucl. Mater. 28, 1 (1968). See also R. Asher et al., Corros. Sci. 10, 695
(1970).
73. Y.-Z. Wang, in Uhlig’s Corrosion Handbook, 2nd edition, R. W. Revie, editor, Wiley,
New York, 2000, p. 221.
74. H. Gough and D. Sopwith, J. Inst. Metals 49, 93 (1932).
75. N. Wadsworth, in Internal Stresses and Fatigue In Metals, G. Rassweiler and W. Grube,
editors, Elsevier, New York, 1959, pp. 382–396.
76. H. Lee and H. Uhlig, Corrosion fatigue of type 4140 high strength steel, Fig. 6, Metall.
Trans. 3, 2952 (1972).
77. D. McAdam, Jr., Proc. Am Soc. Testing Mater. 27 (II), 102 (1927).
78. D. Duquette and H. Uhlig, Trans. Am. Soc. Metals 62, 839 (1969).
79. A. Asphahani, Ph.D. thesis, Department of Materials Science and Engineering, M.I.T.,
Cambridge, MA, February 1975.
80. H. Uhlig, in Corrosion Fatigue, O. Devereux et al., editors, National Association of
Corrosion Engineers, Houston, TX, 1972, p. 270.
81. D. Duquette and H. Uhlig, Trans. Am. Soc. Metals 61, 449 (1968).
82. Y.-Z. Wang, in Uhlig’s Corrosion Handbook, 2nd edition, R. W. Revie, editor, Wiley,
New York, 2000, p. 231.
83. R. L. Martin, in ASM Handbook, Vol. 13A, Corrosion: Fundamentals, Testing, and
Protection, ASM International, Materials Park, OH, 2003, p. 882.
84. H. Gough, J. Inst. Metals 49, 17 (1932).
85. E. Gadd, in International Conference on Fatigue of Metals, Institution of Mechanical
Engineers, London, 1956, p. 658.
86. S. Suresh, Fatigue of Materials, Cambridge Solid State Science Series, Cambridge Uni-
versity Press, Cambridge, U.K., 1991, pp. 363–368.
87. I-Ming Feng and H. Uhlig, J. Appl. Mech. (published by ASME) 21, 395 (1954).
88. M. Fink and U. Hofmann, Z. Anorg. Allg. Chem. 210, 110 (1933); Z. Metallk. 24, 49
(1932).
89. M. L. Bauccio, in ASM Handbook, Vol. 13, Corrosion, ASM International, Materials
Park, OH, 1987, p. 1030.
90. W. Glaeser and I. G. Wright, in ASM Handbook, Vol. 13A, Corrosion: Fundamentals,
Testing, and Protection, ASM International, Materials Park, OH, 2003, p. 324.
91. M. Antler and M. H. Drozdowicz, Wear 74, 27 (1981–1982).
92. P. L. Ko, J. H. Tromp, and M. K. Weckworth, in Materials Evaluations under Fretting
Conditions, STP 780, American Society for Testing and Materials, Philadelphia, 1981,
pp. 86–105.
93. H. H. Uhlig, J. Appl. Mech. 21, 401 (1954).
94. K. H. R. Wright, Proc. Inst. Mech. Eng. 1B, 556 (1952–1953).
GENERAL REFERENCES
Stress-Corrosion Cracking
C. A. Brebbia, V. G. DeGiorgi, and R. A. Adey, editors, Modelling stress corrosion cracking
and corrosion fatigue, Section 5 in Simulation of Electrochemical Processes, WIT Press,
Southampton, U.K., 2005, pp. 215–244.
B. F. Brown, Stress Corrosion Cracking Control Measures, National Association of Corro-
sion Engineers, Houston, TX, 1977.
R. P. Gangloff and M. B. Ives, editors, Environment-Induced Cracking of Metals, Proceed-
ings of the First International Conference on Environment-Induced Cracking of Metals,
October 1988, National Association of Corrosion Engineers, Houston, TX, 1990.
R. H. Jones, editor, Chemistry and Electrochemistry of Corrosion and Stress Corrosion
Cracking: A Symposium Honoring the Contributions of R. W. Staehle, TMS, Warrendale,
PA, 2001.
T. Magnin, editor, Corrosion-Deformation Interactions, CDI ’96, Second International

Conference on Corrosion-Deformation Interactions, Nice, France, 1996, The Institute
of Materials, London, 1997.
R. N. Parkins, Stress corrosion cracking, in Uhlig’s Corrosion Handbook, 2nd edition,
R. W. Revie, editor, Wiley, New York, 2000, pp. 191–204.
Fatigue and Corrosion Fatigue

S. Suresh, Fatigue of Materials, 2nd edition, Cambridge University Press, Cambridge, U.K.,
1998.
Y.-Z. Wang, Corrosion fatigue, in Uhlig’s Corrosion Handbook, 2nd edition, R. W. Revie,
editor, Wiley, New York, 2000, pp. 221–232.
Fretting Corrosion
David W. Hoeppner, V. Chandrasekaran, and Charles B. Elliott III, editors, Fretting Fatigue:
Current Technology and Practices, STP 1367, ASTM, West Conshohocken, PA, 2000.
Materials Evaluation under Fretting Conditions, Special Technical Publication 780,
American Society for Testing and Materials, Philadelphia, 1981.
R. B. Waterhouse, Fretting Corrosion, Pergamon, Oxford, 1972.
R. B. Waterhouse, Fretting Fatigue, Applied Science Publishers, London, 1981.
R. B. Waterhouse, Fretting wear, in ASM Handbook, Vol. 18, Friction, Lubrication, and
Wear Technology, ASM International, Materials Park, OH, 1992, pp. 242–256.
Fretting wear failures, in ASM Handbook, Vol. 11, Failure Analysis and Prevention, ASM
Effects of Radiation
T. R. Allen et al., editors, Proceedings, 22nd Int. Symposium on Effects of Radiation on
Materials, Boston, 2004, STP 1475, ASTM International, West Conshohocken, PA,
2006.
G. S. Was, J. Busby, and P. L. Andresen, Effect of irradiation on stress-corrosion cracking
and corrosion in light water reactors, in ASM Handbook, Vol. 13C, Corrosion: Environ-
ments and Industries, ASM International, Materials Park, Ohio, 2006, pp. 386–414.
Hydrogen Damage
B. Craig, Hydrogen damage, in ASM Handbook, Vol. 13A, Corrosion: Fundamentals,
M. Elboujdaini, Hydrogen-induced cracking and sulfide stress cracking, in Uhlig’s Corro-
sion Handbook, 2nd edition, R. W. Revie, editor, Wiley, New York, 2000, pp. 205–220.
M. Elboujdaini, Test methods for wet H2S cracking, in Uhlig’s Corrosion Handbook, 2nd
R. D. Kane, Corrosion in petroleum refining and petrochemical operations, in ASM Hand-
book, Vol. 13C, Corrosion: Environments and Industries, ASM International, Materials
Park, OH, 2006, pp. 992–998.
PROBLEMS
1. Engell and Bäumel (T. N. Rhodin, editor, Physical Metallurgy of Stress Corro-
sion Fracture, Interscience, New York, 1959, p. 354) reported that cracks in iron
stressed in boiling calcium nitrate solution propagate discontinuously at the
rate of 0.2 mm/s. To what corrosion current density does this rate correspond?
If this rate is typical, what does your answer indicate with regard to the elec-
trochemical mechanism of crack growth?
2. The residual energy of a cold-worked steel as determined calorimetrically is

21 J/g. Calculate the increased tendency in volts for iron to corrode when cold
worked. (Assume that the entropy change is negligible.)
3. The critical potential for stress-corrosion cracking of moderately cold-worked

18–8 stainless steel in deaerated MgCl2 solution at 130°C is −0.145 V
(S.H.E.).
(a) What effect on SCC of 18–8 results from coupling to nickel (φcorr = −0.18 V)?
(d) On adding HCl? Why?
(c) Under (b), below what value of pH at 130°C does the cathode potential of 18–8
become more noble than φcritical?
Answers to Problems
1. 545 A/cm2.
2. 0.006 V.
3. (c) 1.8.
9
ATMOSPHERIC CORROSION
9.1 INTRODUCTION
In the absence of moisture, iron exposed to the atmosphere corrodes at a negli-

gible rate. For example, steel parts abandoned in the desert remain bright and
tarnish-free for long periods of time. Also, the corrosion process cannot proceed
without an electrolyte; hence, in climates below the freezing point of water or of
aqueous condensates on the metal surface, rusting is negligible. Ice is a poor
electrolytic conductor. Incidence of corrosion by the atmosphere depends,
however, not only on the moisture content of air, but also on the particulate
matter content and gaseous impurities that favor condensation of moisture on
the metal surface.
Ambient air quality in the United States has improved dramatically since the
Clean Air Act was enacted in 1970. The Environmental Protection Agency (EPA)
monitors air quality and compares the data with the National Ambient Air
Quality Standards (NAAQS), which have been established for ozone (O3), carbon
monoxide (CO), nitrogen dioxide (NO2), sulfur dioxide (SO2), lead (Pb), and
particulate matter (PM, airborne particles of any composition). Improvements in
air quality help to mitigate atmospheric corrosion, as will be discussed in this
chapter.

191
192 ATMOSPHERIC CORROSION
9.2 TYPES OF ATMOSPHERES
Atmospheres vary considerably with respect to moisture, temperature, and con-

taminants; hence, atmospheric corrosion rates vary markedly around the world.
Approaching the seacoast, air is laden with increasing amounts of sea salt, in
particular NaCl. At industrial areas, SO2, H2S, NH3, NO2, and various suspended
salts are encountered. Approximate concentration ranges of corrosive gases in
urban areas are presented in Table 9.1 [1]. Acids that can form from these gases
include sulfuric acid (H2SO4), nitric acid (HNO3), and organic acids, such as
formic acid (HCOOH) and acetic acid (CH3COOH).
A metal that resists corrosion in one atmosphere may lack effective corrosion
resistance elsewhere; hence, relative corrosion behavior of metals changes with
location; for example, galvanized iron performs well in rural atmospheres, but is
relatively less resistant to industrial atmospheres. On the other hand, lead per-
forms in an industrial atmosphere at least as well as, or better than, elsewhere
because a protective film of lead sulfate forms on the surface.
Recognition of marked differences in corrosivity has made it convenient to
divide atmospheres into types. The major types are marine, industrial, tropical,
arctic, urban, and rural. There are also subdivisions, such as wet and dry tropical,
with large differences in corrosivity. Also, specimens exposed to a marine atmo-
sphere corrode at greatly differing rates depending on proximity to the ocean.
At Kure Beach, North Carolina, specimens of steel located 24 m (80 ft) from the
ocean, where salt water spray is frequent, corroded about 12 times more rapidly
than similar specimens located 240 m (800 ft) from the ocean [2].
9.3 CORROSION-PRODUCT FILMS
Corrosion-product films formed in the atmosphere tend to be protective; that is,

the corrosion rate decreases with time (Fig. 9.1) [3]. This is true to a lesser extent
of pure iron, for which the rate is relatively high, compared to the copper-bearing
or low-alloy steels, which are more resistant. Rust films on the latter steels tend
TABLE 9.1. Atmospheric Corrosive Gases in Outdoor

Urban Environments [1]
Gas Approximate Concentration Range (ppbv)
H2S 0.2–700
SO2 3–1000
NH3 1–90
HCl 0.5–100
NO2 0.5–300
O3 0.9–600
RCOOH 0.5–30
CORROSION-PRODUC T FILMS 193
Figure 9.1. Atmospheric corrosion of steels as a function of time in an industrial environment

(C. Larrabee, in Corrosion Handbook, H. H. Uhlig, editor, Wiley, New York, 1948, p. 124)
to be compact and adherent, whereas on pure iron they are a powdery loose
product. The corrosion rate eventually reaches steady state and usually changes
very little on further exposure. This is characteristic of other metals as well, as
can be seen from data obtained by the American Society for Testing and Materi-
als for various metals exposed 10 or 20 years to several atmospheres (Table 9.2)
[4]. Within the experimental error of such determinations, the rate for a 20-year
period is about the same as that for a 10-year period. The data in Table 9.2 also
show the beneficial effect of alloying elements, primarily 1.1% Cr and 0.4% Cu,
in the low-alloy steel compared to the 0.2% C steel.
Data of Fig. 9.1 follow the relation
p = kt n (9.1)
where p can be expressed as specimen weight loss (g/m2), or as specimen penetra-

tion (μm), during time t (years), and k and n are constants that depend on the
metal and on the atmospheric conditions (i.e., climatic and pollution factors) at
the test site. In addition to carbon steels, this relation is also found to apply to
atmospheric test data for galvanized, aluminized, and 55% Al–Zn coatings on
steel [5–7]. Values of n typically range from about 0.5 to 1. The constant, n = 1,
applies for a linear rate law; that is, the corrosion product film is not protective.
In comparison with carbon steels, weathering steels have very low values of n,
TABLE 9.2. Average Atmospheric Corrosion Rates of Various Metals for 10- and 20-Year
Exposure Times, mils/yeara (American Society for Testing and Materials) [4]
Metal Atmosphere
New York City La Jolla, CA State College,

(Urban (Marine) PA (Rural)
Industrial)
10 20 10 20 10 20
Years Years Years Years Years Years
Aluminum 0.032 0.029 0.028 0.025 0.001 0.003

Copper 0.047 0.054 0.052 0.050 0.023 0.017
Lead 0.017 0.015 0.016 0.021 0.019 0.013
Tin 0.047 0.052 0.091 0.112 0.018 —
Nickel 0.128 0.144 0.004 0.006 0.006 0.009
65% Ni, 32% Cu, 2% Fe, 1% Mn 0.053 0.062 0.007 0.006 0.005 0.007
(Monel)
Zinc (99.9%) 0.202 0.226 0.063 0.069 0.034 0.044
Zinc (99.0%) 0.193 0.218 0.069 0.068 0.042 0.043
0.2% C steelb (0.02% P, 0.05% S, 0.48 — — — — —
0.05% Cu, 0.02% Ni, 0.02% Cr)
Low-alloy steelb (0.1% C, 0.2% P, 0.09 — — — — —
0.04% S, 0.03% Ni, 1.1% Cr,
0.4% Cu)
a
1 mil/year = 0.001 in./year = 0.0254 mm/year = 25.4 μm/year.
b
Kearney, New Jersey (near New York City); values cited are one-half reduction of specimen thickness
[C. P. Larrabee, Corrosion 9, 259 (1953)].
usually less than 21 [8]. A value of n = 0.5 corresponds to a parabolic

rate law.
From (9.1), the linear bilogarithmic law may be expressed as
log p = A + B log t (9.2)
where A = log k and B = n. The atmospheric behavior of a specific metal at a

specific location can be described using the two parameters A and B. This biloga-
rithmic law can be very useful in predicting long-term atmospheric corrosion
damage based on tests of shorter duration. Extrapolation up to 20–30 years from
tests of 4 years is possible with reasonable confidence [9]. Over the longer term,
changes in the environment are likely to be more significant than deviations from
the model.
The mean corrosion rate, p/t, can be calculated as
log ( pt ) = A + B − 1 log t
( ) (9.3)
FAC TORS INFLUENCING CORROSIVIT Y OF THE ATMOSPHERE 195
and the instantaneous corrosion rate, dp/dt, can be expressed as
log ( dpdt ) = A + log B + (B − 1) log t (9.4)
When there is a linear relationship between log p and log t, there are also linear
relationships between log p/t and log t, and between log dp/dt and log t.
Metal surfaces located where they become wet or retain moisture, but where
rain cannot wash the surface, may corrode more rapidly than specimens fully
exposed. The reason for this is that sulfuric acid, for example, absorbed by rust
will continue to accelerate corrosion, perhaps by means of the cycle
1 1 1 1
H 2SO4 + O2 O2 + H 2SO4 1 H 2O 1 3
Fe ⎯⎯⎯⎯⎯ 2
→ FeSO4 ⎯4⎯⎯⎯⎯⎯
2
→ Fe2 (SO4)3 ⎯2⎯⎯→ Fe2O3 + H 2SO4
2 2 2
(9.5)
Intermediate formation of ferric sulfate has not been demonstrated, and so
FeSO4 may oxidize directly to Fe2O3. Nevertheless, rust contaminated in this way
catalyzes the formation of more rust. Direct exposure of a metal to rain may,
therefore, be beneficial, compared to a partially sheltered exposure. This advan-
tage presumably would not extend to uncontaminated atmospheres.
9.4 FACTORS INFLUENCING CORROSIVITY OF THE ATMOSPHERE
In all except the most corrosive atmospheres, the average corrosion rates of
metals are generally lower when exposed to air than when exposed to natural
waters or to soils. This fact is illustrated by the data of Table 9.3 for steel, zinc,
and copper in three atmospheres compared to average rates in seawater and a
TABLE 9.3. Comparison of Atmospheric Corrosion Rates with Average Rates in Seawater
and in Soilsa
Environment Corrosion Rate (gmd)
Steel Zinc Copper
Rural atmosphere — 0.017 0.014

Marine atmosphere 0.29 0.031 0.032
Industrial atmosphere 0.15 0.10 0.029
Seawater 2.5 1.0 0.8
Soil 0.5 0.3 0.07
a 1
Atmospheric tests on 0.3% copper steel, 7 2-year exposure, from C. Larrabee, Corrosion 9, 259 (1953).
Atmospheric rates for zinc and copper, 10-year exposure, from Symposium on Atmospheric Exposure
Tests on Non-Ferrous Metals, ASTM, 1946. Seawater data from Corrosion Handbook, H. H. Uhlig,
editor, Wiley, New York, 1948. Soil data for steel are averaged for 44 soils, 12-year exposure; for zinc,
12 soils, 11-year exposure; for copper, 29 soils, 8-year exposure–from Underground Corrosion, M.
Romanoff, Circ. 579, National Bureau of Standards, Washington, D.C. 1957.
variety of soils. In addition, atmospheric corrosion of passive metals (e.g., alumi-

num and stainless steels) tends to be more uniform and with less marked pitting
than corrosion in waters or soils.
Specific factors influencing the corrosivity of atmospheres are particulate
matter, gases in the atmosphere, and moisture (critical humidity). In the United
States, the Environmental Protection Agency (EPA) compiles data on ambient
outdoor-air quality from information obtained at air-monitoring stations, where
concentrations of the more common gases found in trace amounts in the atmo-
sphere are measured continuously. Because of the importance of trace constitu-
ents on atmospheric corrosion behavior, the engineer or architect would be well
advised to review air-quality data for a corrosion assessment at the design stage,
to avoid disappointment at the operational stage. Microclimatic conditions (e.g.,
east versus west exposure, sunlight, wind direction, proximity to a highway where
deicing salts are used) can be different from macroclimates and should be
considered.
9.4.1 Particulate Matter

Particulate matter (PM) is the term for a mixture of solid particles and liquid
droplets in air. PM consists of several components, including acids, organic chemi-
cals, metals, and soil or dust particles. The importance of atmospheric dust was
established in the early experiments of Vernon [11], who exposed specimens of
iron to an indoor atmosphere, some specimens being entirely enclosed by a cage
of single-thickness muslin measuring several inches larger in size than the speci-
men. After several months, the unscreened specimens showed rust and appre-
ciable gain in weight, whereas the muslin-screened specimens showed no rust
whatsoever and had gained weight only slightly.
Particulate matter is found near roads and some industries, in smoke and
haze; it can be directly emitted from sources such as forest fires, and it can be
formed when gases emitted from power plants and automobiles react in the air.
The NAAQSs for particulate matter, revised in 2006, are set at 150 μg/m3 as the
24-h average for coarse particulates (2.5- to 10-μm diameter) and are set at
35 μg/m3 as the 24-h average for fine particulates (≤2.5-μm diameter) [12]. Particle
pollution is controlled by reducing directly emitted particles and by reducing
emissions of pollutants that are gases when emitted, but form particles in the
atmosphere. In the United States in 2006, the average concentration of fine par-
ticulates amounted to about 13 μg/m3 [13].
Particulate matter can be a primary contaminant of many atmospheres. In
the 1950s, it was estimated that the average city air contained about 2 mg/m3, with
higher values for an industrial atmosphere, reaching 1000 mg/m3 or more [14]. It
was estimated that more than 35,000 kg of dust per km2 (100 tons per square
mile) settled every month over an industrial city [15].
In contact with metallic surfaces, particulate matter influences the corrosion
rate in an important way. Industrial atmospheres carry suspended particles of
carbon and carbon compounds, metal oxides, H2SO4, (NH4)2SO4, NaCl, and other
salts. Marine atmospheres contain salt particles that may be carried many miles
inland, depending on magnitude and direction of the prevailing winds. These
substances, combined with moisture, initiate corrosion by forming galvanic or
differential aeration cells; or, because of their hygroscopic nature, they form an
electrolyte on the metal surface. Dust-free air, therefore, is less apt to cause cor-
rosion than is air heavily laden with dust, particularly if the dust consists of
water-soluble particles or of particles on which H2SO4 is adsorbed.
9.4.2 Gases in the Atmosphere

The carbon dioxide normally present in air neither initiates nor accelerates cor-
rosion. Steel specimens rust in a carbon-dioxide-free atmosphere as readily as in
the normal atmosphere. Early experiments by Vernon showed that the normal
carbon dioxide content of air actually decreases corrosion [16], probably by
favoring a more protective rust film.
A trace amount of hydrogen sulfide in contaminated atmospheres causes the
observed tarnish of silver and may also cause tarnish of copper. The tarnish films
are composed of Ag2S and a mixture of Cu2S + CuS + Cu2O, respectively.
Important atmospheric pollutants are sulfur dioxide (SO2), nitrogen oxides
(NOx), ozone (O3), and chloride ions (Cl−). Sulfur dioxide and nitrogen oxides
form corrosive acids, and ozone is a powerful oxidizing agent.
Sulfur dioxide originates predominantly from the burning of coal, oil, and
gasoline. In New York City in the 1950s, it was estimated that about 1.5 million
tons of sulfur dioxide were produced every year from burning coal and oil [17].
This amount was equivalent to burdening the atmosphere with an average of
6300 tons of H2SO4 every day and has been reduced by limiting the allowable
sulfur content of fuels burned within city limits. Since fuel consumption is
higher in winter, sulfur dioxide contamination is also higher (Fig. 9.2). It is also
obvious from this cause that the average sulfur dioxide content of the air (and
Figure 9.2. Variation of average sulfur dioxide content of New York City air with time of
year [17].
TABLE 9.4. Variation of SO2 Content of Air with Distance from Center of City (H. Meller, J.
Alley, and J. Sherrick, quoted in Ref. 17)
City Parts per Million
Distance 0–5 5–10 10–15 15–20 20–25 25–30

Miles Kilometers 0–8 8–16 16–24 24–32 32–40 40–48
Detroit 0.023 0.012 0.006 0.004 0.004 0.005

Philadelphia–Camden 0.030 0.018 0.016 0.021 0.012 0.012
Pittsburgh 0.060 0.030 0.015 0.018 0.009 0.010
St. Louis 0.111 0.048 0.029 0.020 0.018 0.014
Washington, D.C. 0.003 0.001 0.001 0.001 0.001 0.002
corresponding corrosivity) falls off with distance from the center of an industrial
city, and it is clear that this effect is not as pronounced in the case of a residential
city, such as Washington, D.C. (Table 9.4).
Although the SO2 levels in the air of many major centers of population
around the world may be similar to the data in Fig. 9.2, the engineering and
industrial responses to the U.S. Clean Air Act have resulted in a major decline
in the levels of air pollutants. About 10% of SO2 emissions result from industrial
processes, and transportation sources contribute most of the remainder. The EPA
estimates that ambient SO2 levels have decreased by more than 50% since 1983.
In comparison with the data in Fig. 9.2, the annual average concentration of SO2
in New York City air in 2006 was about 0.01 ppm, and the NAAQS for SO2 is
0.03 ppm (annual arithmetic mean) [18].
A high sulfuric acid content of industrial and urban atmospheres shortens
the life of metal structures (see Tables 9.2 and 9.3). The effect is most pronounced
for metals that are not particularly resistant to sulfuric acid, such as zinc, cadmium,
nickel, and iron. It is less pronounced for metals that are more resistant to dilute
sulfuric acid, such as lead, aluminum, and stainless steels. Copper, forming a pro-
tective basic copper sulfate film, is more resistant than nickel or 70% Ni–Cu alloy,
on which the corresponding films are less protective. In the industrial atmosphere
of Altoona, Pennsylvania, galvanized steel sheets [0.381 kg zinc per m2, 0.028 mm
thick (1.25 oz zinc per ft2, 1.1 mil thick)] began to rust after 2.4 years, whereas in
the rural atmosphere of State College, Pennsylvania, rust appeared only after
14.6 years [19].
Copper exposed to industrial atmospheres forms a protective green-colored
corrosion product called a patina, composed mostly of basic copper sulfate,
CuSO4·3Cu(OH)2. A copper-covered church steeple on the outskirts of a town
may develop such a green patina on the side facing prevailing winds from the
city, but remain reddish-brown on the opposite side, where sulfuric acid is less
readily available. Near the seacoast, a similar patina forms, composed in part of
basic copper chloride.
Industrial atmospheres can cause S.C.C of copper-base alloys, mostly

accounted for by presence of nitrogen oxides (see Section 20.2.3). Copper did
not fail, but copper alloys containing >20% Zn failed on exposures for up to 8
years [20].
Nickel is quite resistant to marine atmospheres, but is sensitive to sulfuric
acid of industrial atmospheres (Table 9.2), forming a surface tarnish composed
of basic nickel sulfate. Corrosion in the industrial atmosphere of New York City
is about 30 times higher than in the marine atmosphere of La Jolla, California,
and about 20 times higher than in the rural atmosphere of State College,
Pennsylvania (Table 9.2).
9.4.3 Moisture (Critical Humidity)

From previous discussions, it is apparent that, in an uncontaminated atmo-
sphere at constant temperature, appreciable corrosion of a pure metal surface
would not be expected at any value of relative humidity below 100%. Practi-
cally, however, because of normal temperature fluctuations (relative humidity
increases on decrease of temperature) and because of hygroscopic impurities
in the atmosphere or in the metal itself, the relative humidity must be reduced
to values much lower than 100% in order to ensure that no water condenses
on the surface. In very early studies, Vernon discovered that a critical relative
humidity exists below which corrosion is negligible [21]. Experimental
values for the critical relative humidity are found to fall, in general, between
50% and 70% for steel, copper, nickel, and zinc. Typical corrosion behavior of
iron as a function of relative humidity of the atmosphere is shown in Fig. 9.3.
In a complex or severely polluted atmosphere, a critical humidity may not
exist [22].
An important factor determining susceptibility to atmospheric corrosion of
a metal in a particular environment is the percentage of time that the critical
humidity is exceeded [23]. This period of time is called the “time of wetness.” It
is determined by measuring the potential between a corroding metal specimen
and a platinum electrode [23, 24]. Surface moisture from either precipitation or
condensation is the cell electrolyte. To estimate atmospheric corrosion rates,
Kucera et al. designed the device shown in Fig. 9.4 [25, 26]. The cell B is placed
about 1 m above ground level with the surface inclined at 45 °. An electronic
integrator automatically integrates cell currents over extended periods of time.
Calibration using data from weight-loss experiments at the same site shows that
the electrochemical technique is suitable for estimating short-term variations in
corrosion rates [26].
Atmospheric corrosion testing is important to the suppliers of metals and to
the engineers and architects who use metals under atmospheric conditions.
Reviews have been prepared summarizing the atmospheric corrosion standards
and testing procedures of the American Society for Testing and Materials
[27–30].
Figure 9.3. Corrosion of iron in air

containing 0.01% SO2, 55 days’ exposure,
showing critical humidity [21].
Figure 9.4. General arrangement of electrochemical device for measurement of atmospheric

corrosion: A is a zero resistance ammeter, the circuit of which is shown on the right; B is an
electrochemical cell with (a) electrodes and (b) insulators; C is an external emf. [25, 26]. (Copy-
right ASTM INTERNATIONAL. Reprinted with permission.)
REMEDIAL MEASURES 201
9.5 REMEDIAL MEASURES
1. Use of Organic, Inorganic, or Metallic Coatings. Coatings are discussed in

Chapters 14, 15, and 16.
2. Reduction of Relative Humidity. Heating air—or, better still, reducing the
moisture content—can reduce relative humidity. Lowering the relative
humidity to 50% suffices in many cases. If the presence of unusually
hygroscopic dust or other surface impurities is suspected, the value should
be reduced still further. This protective measure is effective except perhaps
when corrosion is caused by acid vapors from nearby unseasoned wood
or by certain volatile constituents of adjacent plastics, or paints.
3. Use of Vapor-Phase Inhibitors and Slushing Compounds. These are dis-
cussed in Chapter 17.
4. Use of Alloys. When alloyed with steel in small concentrations, copper,
phosphorus, nickel, and chromium are particularly effective in reducing
atmospheric corrosion. Copper additions are more effective in temperate
climates than in tropical marine regions; chromium and nickel additions
combined with copper and phosphorus are effective in both locations
(Table 9.5). Corrosion rates of structural steels in tropical atmospheres
(e.g., Panama) were found, in general, to be about two or more times
higher than in temperate atmospheres (e.g., Kure Beach, North Carolina)
mainly because of the higher relative humidity and higher average
temperatures.
The usefulness of low-alloy steels to resist atmospheric corrosion through

formation of protective rust films has resulted in the development of weathering
steels. These are used for construction of buildings and bridges and for architec-
tural trim, without the necessity of painting, thereby saving appreciable amounts
in maintenance costs over the life of the structure. A typical commercial composi-
tion is as follows: 0.09% C, 0.4% Mn, 0.4% Cu, 0.8% Cr, 0.3% Ni, 0.09% P. Such
steels do not have any advantage when buried in soil or totally immersed in water,
because the corresponding rust films formed under continuously wet conditions
are no more protective than those formed on carbon steels. Their more noble
corrosion potentials compared to carbon steels may make them useful in certain
galvanic couples (see Section 7.3.2.1). It is only by a process of alternate wetting
and drying that the rust continues to be protective.
Misawa et al. [32] proposed that an inner cohesive protective rust film is
formed on low-alloy steels after long atmospheric exposure (industrial or urban).
It consists of amorphous δ-FeOOH, the formation of which is catalyzed by copper
and phosphorus on the steel surface; alternate drying and wetting favors its pro-
tective qualities. Keiser et al. [33] confirmed that the typical inner adherent rust
layer consists mostly of δ-FeOOH.
Stainless steels and aluminum resist tarnish in industrial, urban, and rural
atmospheres, as is apparent from their satisfactory use over many years as
TABLE 9.5. Effect of Low-Alloy Components on Atmospheric Corrosion of Commercial

Steel Sheet (Eight-Year Exposure)
Steel Composition, % Loss of
Thickness
C P Cu Other mm mils
Industrial Atmosphere (Kearney, NJ) [19]

Carbon 0.2 0.02 0.03 0.20 8.0
Copper bearing 0.2 0.02 0.3 0.11 4.4
Low chromium 0.09 0.2 0.4 1 Cr 0.048 1.9
Low nickel 0.2 0.1 0.7 1.5 Ni 0.051 2.0
Temperate Marine Atmospherea(Kure Beach, NC) [19]

Carbon 0.2 0.02 0.03 0.24 9.5
Copper bearing 0.2 0.01 0.2 0.15 5.8
Low chromium 0.1 0.14 0.4 1 Cr 0.069 2.7
Low nickel 0.1 0.1 0.7 1.5 Ni 0.076 3.0
Tropical Marine Atmosphere (Panama Canal Zone) [31]

Carbon 0.25 0.08 0.02 0.52 20.4
Copper bearing 0.2 0.004 0.24 0.45 17.6
Low chromium 0.07 0.008 0.1 3.2 Cr 0.23 9.1
Low nickel 0.2 0.04 0.6 2.1 Ni 0.19 7.5
a
7.5-year exposure.
architectural trim of buildings. Hastelloy C (54% Ni, 17% Mo, 5% Fe, 15% Cr,
4% W) is very resistant to tarnish in marine atmospheres, making it a useful alloy
for reflectors on board ship.
REFERENCES
1. C. Leygraf and T. Graedel, Atmospheric Corrosion, Wiley, New York, 2000, p. 41.
2. F. L. LaQue, Am. Soc. Testing Mater. Proc. 51, 495 (1951).
3. C. P. Larrabee and S. K. Coburn, in Proceedings, First International Congress On Metallic
Corrosion, Butterworths, London, 1962, pp. 276–284.
4. Symposium on Atmospheric Corrosion of Non-Ferrous Metals, STP 175, American
Society for Testing Materials, Philadelphia, PA, 1955. Also previous Symposium,
1946.
5. M. Tullmin and P. R. Roberge, Atmospheric corrosion, in Uhlig’s Corrosion Handbook,
2nd edition, R. W. Revie, editor, Wiley, New York, 2000, pp. 315–317.
6. R. Legault and V. Pearson, Corrosion 34, 433 (1978).
7. H. Townsend and J. Zoccola, Mater. Perf. 18(10), 13 (1979).
8. L. Veleva and R. D. Kane, in ASM Handbook, Vol. 13A, Corrosion: Fundamentals,
9. T. Kodama, in ASM Handbook, Vol. 13B, Corrosion: Materials, ASM International,

10. M. Pourbaix, The linear bilogarithmic law for atmospheric corrosion, in Atmospheric
Corrosion, W. H. Ailor, editor, Wiley, New York, 1982, pp. 107–121.
11. W. Vernon, Trans. Faraday Soc. 23, 113 (1927).
12. http://www.epa.gov/oar/particlepollution/naaqsrev2006.html
13. http://www.epa.gov/air/airtrends/pm.html
14. A. Kutzelnigg, Werks. Korros. 8, 492 (1957).
15. Chem. Eng. News, January 4, 1971, p. 29.
16. W. Vernon, Trans. Faraday Soc. 31, 1668 (1935).
17. L. Greenburg and M. Jacobs, Eng. Chem. 48, 1517 (1956).
18. http://www.epa.gov/air/airtrends/sulfur.html
19. C. P. Larrabee, Corrosion 9, 259 (1953).
20. J. Popplewell and T. Gearing, Corrosion 31, 279 (1975).
21. W. Vernon, Trans. Faraday Soc. 23, 113 (1927); ibid., 27, 255 (1931) and 31, 1668 (1935);
Trans. Electrochem. Soc. 64, 31 (1933).
22. D. Rice, P. Phipps, and R. Tremoureux, J. Electrochem. Soc. 126, 1459 (1979); 127, 563
(1980).
23. P. Sereda, in Corrosion In Natural Environments, STP 558, American Society for
Testing and Materials, Philadelphia, 1974, p. 7.
24. F. Mansfeld, in Atmospheric Corrosion, W. Ailor, editor, Wiley, New York, 1982, p. 139.
25. V. Kucera and E. Mattsson, in Ref. 23, p. 239.
26. V. Kucera and M. Collin, In Eurocorr ’77, Sixth European Congress On Metallic Cor-
rosion, London, 1977, Society of Chemical Industry, London, 1977, p. 189.
27. W. Ailor, in Atmospheric Factors Affecting the Corrosion of Engineering Metals, S.
Coburn, editor, STP 646, American Society for Testing and Materials, Philadelphia,
1978, p. 129.
28. S. Dean, in Ref. 24, p. 195.
29. H. H. Lawson, Outdoor atmospheres, in Corrosion Tests and Standards: Application
and Interpretation, 2nd edition, R. Baboian, editor, ASTM International, West
Conshohocken, 2005, pp. 343–348.
30. J. D. Sinclair, Indoor atmospheres, in Corrosion Tests and Standards: Application and
Interpretation, 2nd edition, R. Baboian, editor, ASTM International, West
Conshohocken, 2005, pp. 349–361.
31. C. Southwell, B. Forgeson, and A. Alexander, Corrosion 14, 435t (1958).
32. T. Misawa, T. Kyuno, W. Suetaka, and S. Shimodaira, Corros. Sci. 11, 35 (1971).
33. J. Keiser, C. Brown, and R. Heidersbach, Corros. Sci. 23, 251 (1983).
GENERAL REFERENCES
W. Ailor, editor, Atmospheric Corrosion, Wiley, New York, 1982.

R. B. Griffin, Corrosion in marine atmospheres, in ASM Handbook, Vol. 13C, Corrosion:
Environments and Industries, ASM International, Materials Park, OH, 2006, pp.
42–60.
C. Leygraf, Atmospheric corrosion, in Corrosion Mechanisms in Theory and Practice, 2nd

edition, P. Marcus, editor, Marcel Dekker, New York, 2002.
C. Leygraf and T. Graedel, Atmospheric Corrosion, Wiley-Interscience, New York, 2000.
C. Leygraf, J. Hedberg, P. Qiu, H. Gil, J. Henriquez, and C. M. Johnson, Molecular in situ
studies of atmospheric corrosion, Corrosion 63(8), 715 (2007).
P. R. Roberge, Corrosion inspection and Monitoring, Wiley Series In Corrosion, R. W. Revie,
series editor, Wiley, New York, 2007, pp. 301–311.
L. S. Selwyn and P. R. Roberge, Corrosion of metal artifacts displayed in outdoor environ-
ments, in ASM Handbook, Vol. 13C, Corrosion: Environments and Industries, ASM
M. Tullmin and P. R. Roberge, Atmospheric corrosion, in Uhlig’s Corrosion Handbook, 2nd
L. Veleva and R. D. Kane, Atmospheric corrosion, in ASM Handbook, Vol. 13A, Corrosion:
Fundamentals, Testing, and Protection, ASM International, Materials Park, OH, 2003,
pp. 196–209.
PROBLEMS
1. A carbon steel is exposed to a highly polluted, industrial-marine environment.

After one year of exposure, the penetration is 130 μm, and after 4 years, the
penetration is 190 μm. Assuming the bilogarithmic law applies, calculate the
following:
(a) The constants A and B in Eq. (9.2).
(b) The average corrosion rate, in terms of penetration per year, over a 40-year period,
assuming that environmental conditions do not change significantly during this
time period.
(c) The instantaneous corrosion rate, in terms of penetration per year, at 5, 25, and 40
years of exposure.
2. A weathering steel is exposed to the same environment as the carbon steel in

Problem 1. After one year of exposure the penetration is 25 μm, and after four
years the penetration is 28 μm. Assuming the bilogarithmic law applies, calcu-
late the following:
(a) The constants A and B in Eq. (9.2).
(b) The average corrosion rate, in terms of penetration per year, over a 40-year period,
assuming that environmental conditions do not change significantly during this
time period.
(c) The instantaneous corrosion rate, in terms of penetration per year, at 5, 25, and 40
years of exposure.
10
CORROSION IN SOILS
10.1 INTRODUCTION
There are more than 3.7 million kilometers (2.3 million miles) of pipelines cross-
ing the United States, transporting natural gas and hazardous liquids from sources
such as wells, refineries, and ports to customers [1]. Underground corrosion is of
major importance and results in a significant portion of pipeline failures [1].
Because of corrosion, these pipelines must be regularly inspected, maintained,
and sometimes replaced.
In soils, water and gas occupy the spaces between solid particles, and these
spaces can constitute as much as half the volume of dry soil. Some of this water
is bound to mineral surfaces, whereas bulk water can flow through porous soil.
Fluid flow through soil is controlled by the permeability of the soil, which, in turn,
depends on the size distribution of the solid particles in the soil. Coarse-grained
sand, for example, allows good drainage and access of atmospheric oxygen to a
depth greater than, for example, fine-grained soils high in clay. Capillary action
in fine-grained soil can draw water up, keeping the soil water-saturated, prevent-
ing drainage, retarding evaporation, and restricting oxygen access from the atmo-
sphere to a buried structure, such as a pipeline [2].

205
206 CORROSION IN SOILS
The electrochemical corrosion processes that take place on metal surfaces in

soils occur in the groundwater that is in contact with the corroding structure.
Both the soil and the climate influence the groundwater composition. For example,
some clay soils buffer the groundwater pH [2]. Groundwater in desert regions
can be high in chloride and very corrosive. On the other hand, groundwaters in
tropical climates tend to be very acidic. The influence of soil on groundwater
composition is discussed in detail elsewhere [3].
The corrosion behavior of iron and steel buried in the soil approximates, in
some respects, the behavior on total immersion in water. Minor composition
changes and structure of a steel, for example, are not important to corrosion resis-
tance. Hence, a copper-bearing steel, a low-alloy steel, a mild steel, and wrought
iron are found to corrode at approximately the same rate in any given soil. In addi-
tion, cold working or heat treatment do not affect the rate. Gray cast iron in soils,
as well as in water, is subject to graphitic corrosion. Galvanic effects of coupling
iron or steel of one composition to iron or steel of a different composition are
important, because they are under conditions of total immersion (Section
7.3.2.1).
In other respects, corrosion in soils resembles atmospheric corrosion in that
observed rates, although usually higher than in the atmosphere, vary to a marked
degree with the type of soil. A metal may perform satisfactorily in some parts of
the country, but not elsewhere, because of specific differences in soil composition,
pH, moisture content, and so on. For example, a cast iron water pipe may last
50 years in New England soil, but only 20 years in the more corrosive soil of
southern California.
Corrosion rates underground have been measured using the Stern–Geary
linear polarization method (Section 5.8) as well as weight loss [4]. The former
method has been useful, for example, in assessing the corrosion rates of footings
of galvanized-steel towers used to support power lines [5].
10.2 FACTORS AFFECTING THE CORROSIVITY OF SOILS
Among the factors that control corrosivity of a given soil are (1) porosity (aera-
tion), (2) electrical conductivity or resistivity, (3) dissolved salts, including depo-
larizers or inhibitors, (4) moisture, and (5) pH. Each of these variables may affect
the anodic and cathodic polarization characteristics of a metal in a soil. A porous
soil may retain moisture over a longer period of time or may allow optimum
aeration, and both factors tend to increase the initial corrosion rate. The situation
is more complex, however, because corrosion products formed in an aerated soil
may be more protective than those formed in an unaerated soil. In most soils,
particularly if not well-aerated, observed corrosion takes the form of deep pitting.
Localized corrosion of this kind is obviously more damaging to a pipeline than
a higher overall corrosion rate occurring more uniformly. Another factor to be
considered is that, in poorly aerated soils containing sulfates, sulfate-reducing
bacteria may be active; these organisms often produce the highest corrosion rates
normally experienced in any soil.
BUREAU OF STANDARDS TESTS 207
Aeration of soils may affect corrosion not only by the direct action of oxygen
in forming protective films, but also indirectly through the influence of oxygen
reacting with and decreasing the concentration of the organic complexing agents
or depolarizers naturally present in some soils. In this regard, the beneficial effect
of aeration extends to soils that harbor sulfate-reducing bacteria because these
bacteria become dormant in the presence of dissolved oxygen. Corrosion rates
tend to increase with depth of burial near the soil surface, but not invariably.
Bureau of Standards tests [6] on steel specimens exposed 6–12 years and buried
30–120 cm (12–48 in.) below the surface showed greater corrosion at greater
depth for five soils, but showed the reverse trend for two soils.
A soil containing organic acids derived from humus is relatively corrosive to
steel, zinc, lead, and copper. The measured total acidity of such a soil appears to
be a better index of its corrosivity than pH alone. High concentrations of sodium
chloride and sodium sulfate in poorly drained soils, such as are found in parts of
southern California, make the soil very corrosive. Macrogalvanic cells or “long-
line” currents established by oxygen concentration differences, by soils of differ-
ing composition, or by dissimilar surfaces on the metal become more important
when electrical conductivity of the soil is high. Anodes and cathodes may be
thousands of feet, or even miles, apart. A poorly conducting soil, whether from
lack of moisture or lack of dissolved salts or both, is, in general, less corrosive
than a highly conducting soil. But conductivity alone is not a sufficient index of
corrosivity; in accordance with the principles of electrode kinetics discussed in
Chapter 5, anodic and cathodic polarization characteristics of a corroding metal
in the soil are also a factor.
From studies at the National Physical Laboratory in the United Kingdom, it
was concluded that the corrosivity of soil towards ferrous metals could be esti-
mated by measuring the resistivity of the soil and the potential of a platinum
electrode in the soil with respect to a saturated calomel reference electrode [7].
Soils of low resistivity (<2000 Ω-cm) were considered to be aggressive. Soils in
which the potential at pH 7 was low [<0.40 V (S.H.E.), or <0.43 V if the soil is
clay] were considered to provide a suitable environment for sulfate-reducing
bacteria and to be aggressive. Borderline cases by these two criteria were resolved
by considering that a water content of more than 20% causes a soil to be
aggressive.
10.3 BUREAU OF STANDARDS TESTS
The most extensive series of field tests on various metals and coatings in almost
all types of soils were begun in 1910 by K. H. Logan of the National Bureau of
Standards (now the National Institute of Standards and Technology). These tests
continued until 1955 and now constitute the most important source of informa-
tion on soil corrosion available [6]. They showed similarity in corrosion rates in
a given soil for various kinds of iron and steels; confirmation was obtained
through 5-year tests in England [8]. A few typical corrosion rates averaged for
many soils are listed in Table 10.1. In addition, data are listed for two soils rela-
tively corrosive to steel and for one that is relatively noncorrosive, showing the
large variations in corrosion rate from one soil to another. For San Diego soil,
the symbol > means that the thickness of test specimen was completely pene-
trated by pitting at the end of the exposure period.
Referring again to Table 10.1, we see that copper, on average, corrodes at
about one-sixth the rate of iron, but, in tidal marsh, for example, the rate is com-
paratively higher than in most other soils, being one-half that of iron. The rate
for copper is normal in otherwise corrosive San Diego soil. Pitting is not pro-
nounced, with the maximum depth reaching less than 0.15 mm (6 mils).
Lead also corrodes less on the average than does steel. In poorly aerated
soils or soils high in organic acids, the corrosion rate may be much higher (four
to six times) than the average. Pitting in some of these soils penetrated the test
specimen thickness, accounting for an average maximum penetration greater
than the average given in Table 10.1. Zinc also pitted in some soils to an extent
greater than the specimen thickness. In 5-year tests carried out in Great Britain,
commercially pure aluminum was severely pitted in four soils (0.1 to >1.6 mm,
4 to >63 mils), but was virtually unattacked in a fifth soil [9].
Increase in chromium content of steel decreases observed weight loss in a
variety of soils; but, above 6% Cr, depth of pitting increases. In 14-year tests, 12%
Cr and 18% Cr steels were severely pitted. The 18% Cr, 8% Ni, Type 304 stainless
steel was not pitted or was only slightly pitted (<0.15 mm, <6 mils), nor was weight
loss appreciable in 10 out of 13 soils. However, in three soils, at least one speci-
men was perforated [0.4–0.8 mm (16–32 mils) thick] by pitting. Type 316 stainless
steel did not pit in any of the 15 soils to which the alloy was exposed for 14 years.
It is expected, however, that pitting would also occur with this alloy in longer
time tests since pitting occurs in seawater within about 2 21 years.
Zinc coatings are effective in reducing weight loss and pitting rates of steel
exposed to soils. In 10-year tests in 45 soils, coatings of 0.85 kg/m2 (2.8 oz/ft2) based
on one side of the specimen (0.13 mm or 5 mils thick) protected steel against
pitting with the exception of one soil (Merced silt loam, Buttonwillow, California)
in which some penetration of the base steel could be measured. In later tests
extending up to 13 years, a coating of 0.95 kg/m2 (3.1 oz/ft2) effectively reduced
(but did not prevent) corrosion, even in cinders in which the zinc coating was
destroyed within the first two years.
Cinders constitute one of the most corrosive environments. For 4- or 5-year
exposures, corrosion rates of steel and zinc in cinders was 5 times, copper 8 times,
and lead 20 times higher than the average rates in 13 different soils.
10.3.1 Pitting Characteristics

Because the dimensions of all field test specimens were on the order of inches
up to about 1 ft (3–30 cm), the reported pitting rates represent minimum rather
than maximum values. Actual depth of pits in a given time is found to increase
with size of test specimen, probably because cathodic area per pit increases (i.e.,
TABLE 10.1. Corrosion of Steels, Copper, Lead, and Zinc in Soils (National Bureau of Standards [6])
Maximum Penetration in mils (1 mil = 0.001 in. = 0.025 mm) for Total Exposure Period
Average corrosion rates in g m−2 d−1 (gmd)
BUREAU OF STANDARDS TESTS
Soil Open Wrought Bessemer Copper, Lead, Zinc,

Hearth Iron, Iron, Steel, 8-Year 12-Year 11-Year
12-Year 12-Year 12-Year Exposure Exposure Exposure
Exposure Exposure Exposure
gmd mils gmd mils gmd mils gmd mils gmd mils gmd mils
Average of several soils 0.45 70 0.47 59 0.45 61 0.07 <6 0.052 >32 0.3 >53
(44 soils) (44 soils) (44 soils) (29 soils) (21 soils) (12 soils)
Tidal marsh, Elizabeth, New Jersey 1.08 90 1.16 80 1.95 100 0.53 <6 0.02 13 0.19 36
Montezuma clay, Adobe, San Diego 1.37 >145 1.34 >132 1.43 >137 0.07 <6 0.06 10 — —
(9.6 years)
Merrimac gravelly sandy loam, 0.09 28 0.10 23 0.10 21 0.02 <6 0.013 19 — —
Norwood, Massachusetts (13.2 years)
209
anode/cathode area ratio decreases), thus accounting for higher current densities
at the pits. In addition to this factor, long-line currents or macrocells, if present,
increase pit depth over the values obtained on small specimens where such cells
do not operate.
The rate at which pits grow in the soil under a given set of conditions tends
to decrease with time and follows a power-law equation P = ktn, where P is the
depth of the deepest pit in time t, and k and n are constants. It has been reported
[10] that values of n for steels range from about 0.1 for a well-aerated soil, to 0.9
for a poorly aerated soil. The smaller the value of n, the greater the tendency for
the pitting rate to fall off with time. As n approaches unity, the pitting rate
approaches a constant value, or penetration is proportional to time.
Pits tend to develop more on the bottom side of a pipeline than on the top
side. This difference is sometimes sufficiently great to make it worthwhile rotating
a pipeline 180 ° after a given period of exposure in order to increase pipe life.
Pitting on the bottom side results from constant contact with the soil, whereas
the top side, because of the pipe settling, tends to become detached, producing
an air space between the pipe and the soil.
10.4 STRESS-CORROSION CRACKING
Stress-corrosion cracking (S.C.C.) is a well-known cause of underground oil and

gas transmission pipeline failures [11]. Stress-corrosion cracking of cathodically
protected pipelines originates on the outer pipe surface, most commonly at areas
where the coating is disbonded (i.e., no longer attached to the surface of the steel
pipe).
In most engineering structures where cathodic protection is used to protect
steel from general corrosion, the steel is polarized to a potential of −0.85 V versus
Cu/CuSO4, corresponding to −0.53 V (S.H.E.). Cathodic protection of under-
ground pipelines can result in the accumulation of alkali at the pipe surface [12],
consisting of sodium hydroxide and carbonate/sodium bicarbonate solutions.
Hydrogen ions, cations (e.g., Na+), and water containing dissolved oxygen migrate
to the cathodic pipe surface (via pores or defects in the coating). The reaction in
aerated near-neutral solution at the pipe surface is
O2 + 2 H 2O + 4e − → 4OH − (10.1)
Carbon dioxide from either the air, surrounding water, or decaying vegetation
may then react with the hydroxide forming bicarbonates and carbonates
[13]:
CO2 + OH − → HCO−3 (10.2)
HCO−3 + OH − → CO23− + H 2O (10.3)

REMEDIAL MEASURES 211
The potential range at which stress-corrosion cracks form in carbonate solu-

tions is reported as noble to the optimum cathodic protection potential and
active to the corrosion potential; for example, one high-strength (541 MPa,
78,000 psi yield strength) linepipe steel developed intergranular cracks between
−0.31 and −0.46 V (S.H.E.) in 1 N Na2CO3 + 1 N NaHCO3 solution at 40 °C
[14]. Accumulation of NaOH can also cause S.C.C. in a more active potential
range. In 35% NaOH at 85 °C, S.C.C. of steel is maximum in the region of
−0.7 V (S.H.E.), whereas in ammonium carbonate solution at 70 °C, the
maximum susceptibility occurs near −0.3 V (S.H.E.) (see Figs. 8.6 and 8.7,
Section 8.3.5). From these potential relations, one could assume that NaOH is
more likely to be the cause of failure in sections of pipeline that are cathodi-
cally overprotected, whereas carbonates would be the more likely cause in less
active potential regions.
In addition to the intergranular S.C.C. that occurs in high-pH solutions,
transgranular cracking has been found to occur in dilute aqueous solutions of
near neutral pH [15].
10.5 REMEDIAL MEASURES
1. Organic and Inorganic Coatings. Paint coatings of thickness normal to

atmospheric protection fail within months when exposed to the soil. On
the other hand, thickly applied coatings of coal tar, with reinforcing pig-
ments or inorganic fibers to reduce cold flow, are found to be practical.
They provide effective protection at reasonable cost. Bureau of Standards
tests showed that soft rubber coatings 6 mm (0.25 in.) thick afforded excel-
lent protection to steel in 11-year exposure tests.
Coatings based on bituminous compositions offer excellent service but are
now being supplemented by others—for example, fusion-bonded epoxy
resin typically 1 mm thick applied at the pipe mill.
2. Metallic Coatings. The effectiveness of zinc coatings has already been
mentioned. Such coatings deteriorate more rapidly when galvanically
coupled to large areas of bare iron, steel, or copper, in which case insulat-
ing couplings can be useful.
3. Alteration of Soil. A soil high in organic acids can be made less corrosive
by surrounding the metal structure with limestone chips. A layer of chalk
(CaCO3) surrounding buried pipes has been used in some soil formations
likely to produce microbiologically influenced corrosion [16].
4. Cathodic Protection. In general, buried pipelines and tanks are protected
by a combination of cathodic protection and an organic coating. This
combination protects steel against corrosion in all soils, both effectively
and economically, for as many years as cathodic protection is adequately
maintained.
REFERENCES
1. R. E. Ricker, Analysis of Pipeline Steel Corrosion Data from NBS (NIST) Studies
Conducted between 1922–1940 and Relevance to Pipeline Management, NISTIR 7415,
National Institute of Standards and Technology, U.S. Department of Commerce, May
2, 2007, pp. 1–2.
2. M. J. Wilmott and T. R. Jack, in Uhlig’s Corrosion Handbook, 2nd edition, R. W. Revie,
3. W. Stumm and J. J. Morgan, Aquatic Chemistry: Chemical Equilibria and Rates in
Natural Waters, 3rd edition, Wiley, New York, 1996.
4. D. A. Jones, in Underground Corrosion, E. Escalante, editor, Special Technical Publca-
tion No. 741, American Society for Testing and Materials, Philadelphia, 1981, pp.
123–132.
5. P. H. Hewitt and W. B. R. Moore, in Eurocorr ’77, Sixth European Congress On
Metallic Corrosion, London, 1977, Society of Chemical Industry, London, 1977,
pp. 205–211.
6. M. Romanoff, Underground Corrosion, Circ. 579, U.S. National Bureau of Standards,
1957; reprinted with a Preface by John A. Beavers, NACE, Houston, Texas, 1989; see
also the reexamination and analysis of the original data, Richard E. Ricker, Analysis
of Pipeline Steel Corrosion Data from NBS (NIST) Studies Conducted between 1922–
1940 and Relevance to Pipeline Management, NISTIR 7415, National Institute of
Standards and Technology, U.S. Department of Commerce, May 2, 2007.
7. G. H. Booth, Microbiological Corrosion, M&B Monographs CE/1, Mills & Boon,
London, 1971, pp. 46–49.
8. J. C. Hudson and G. Acock, in Corrosion of Buried Metals, Iron and Steel Institute
Special Report 45, London, 1952.
9. P. Gilbert and F. Porter, in Corrosion of Buried Metals, Iron and Steel Institute, Special
Report 45, London, 1952.
10. Ref. 6, p. 39.
11. Public Inquiry Concerning Stress Corrosion Cracking on Canadian Oil and Gas
Pipelines, Report of the Inquiry, Report MH-2-95, National Energy Board, Calgary,
Alberta, November 1996.
12. W. J. Schwerdtfeger and R. J. Manuele, J. Natl. Bur. Std. (U.S.) 65C, 171 (1961).
13. W. E. Berry, T. J. Barlo, J. H. Payer, R. R. Fessler, and B. L. McKinney, Paper No. 64,
Corrosion/78, National Association of Corrosion Engineers, Houston, TX, 1978.
14. R. Revie and R. Ramsingh, Can. Metall. Q. 22, 235 (1983).
New York, 2000, pp. 191–194.
16. U. R. Evans, The Corrosion and Oxidation of Metals, Arnold, London, 1960, p. 272.
GENERAL REFERENCES
E. Escalante, editor, Underground Corrosion, Special Technical Publication 741, ASTM,

Philadelphia, 1981.
R. E. Ricker, Analysis of Pipeline Steel Corrosion Data from NBS (NIST) Studies Con-
ducted between 1922–1940 and Relevance to Pipeline Management, NISTIR 7415,
National Institute of Standards and Technology, U.S. Department of Commerce, May
2, 2007.
W. Stumm and J. J. Morgan, Aquatic Chemistry: Chemical Equilibria and Rates in Natural
Waters, 3rd edition, Wiley, New York, 1996.
M. J. Wilmott and T. R. Jack, in Uhlig’s Corrosion Handbook, 2nd edition, R. W. Revie,
11
OXIDATION
11.1 INTRODUCTION
In high-temperature corrosion, the protective oxide films—usually either chromia,

Cr2O3, or alumina, Al2O3—that form between the metal and the environment
are of critical importance. One of the major advances in corrosion science
over the past few decades has been the characterization of the reactive element
effect (REE), which identifies the role of small additions of reactive elements,
such as yttrium, hafnium, lanthanum, zirconium, and cerium, to improve high-
temperature oxidation resistance.
Because increasing the temperature of most high-temperature processes
(e.g., energy conversion, waste incineration, chemical synthesis) results in
increased efficiency, there is a high priority for designers and engineers to increase
process temperatures, not only to increase efficiency, but also to reduce emissions,
thereby helping to achieve sustainability and improving economics. For example,
partially insulating the combustion chamber on a Diesel engine increased the
piston surface temperature from 450 °C to 900 °C, and it also increased the com-
bustion efficiency (decreased fuel consumption) by 20% and reduced the non-
burned hydrocarbons emission [1, 2]. Because of the present trend to increase
process temperatures, it is more important than ever for engineers to understand

215
216 OXIDATION
the principles of high-temperature corrosion, the limitations of materials, and the

methods that are being used to improve the performance of engineering materi-
als at high temperatures. The basics of these matters will be explored in this
chapter.
When a metal is exposed at room or elevated temperatures to an oxidizing
gas, such as oxygen, sulfur, or halogens, corrosion may occur in the absence of a
liquid electrolyte. This is sometimes called “dry” corrosion, in contrast to “wet”
corrosion, which occurs when a metal is exposed to water or to the soil. In dry
corrosion, reaction products can be solid films or scales (a scale is a thick film),
liquids, or volatile compounds. When a protective scale—such as alumina (Al2O3),
chromia (Cr2O3), or silica (SiO2)—forms, the metal, the environment, or both
must diffuse through the scale in order for the reaction to continue. Usually ions,
rather than atoms, migrate through solid oxides, sulfides, or halides; hence, the
reaction product can be considered an electrolyte. For copper oxidizing in O2, or
silver tarnishing in a contaminated atmosphere, the solid electrolytes are Cu2O
and Ag2S, respectively. The migrating ions are not hydrated, and they diffuse
simultaneously with electrons, but along different paths.
11.2 INITIAL STAGES
The processes that take place at a clean, reactive metal surface exposed to
oxygen obey the following sequence: (1) adsorption of oxygen, (2) formation
of oxide nuclei that grow laterally, and (3) growth of a continuous oxide film.
Because the free energy of adsorption of atomic oxygen exceeds the free energy
of dissociation of oxygen, the first-formed adsorbed film consists of atomic
oxygen. Low-energy electron-diffraction data show that some metal atoms
enter the approximate plane of adsorbed oxygen to form a relatively stable two-
dimensional structure of mixed O ions (negative) and metal ions (positive). As
was discussed earlier in relation to the passive film (Section 6.5), this initial
adsorbed partial monolayer is thermodynamically more stable than the metal
oxide; for example, for nickel, the adsorbed film resists decomposition up to the
melting point of nickel [3], whereas NiO decomposes accompanied by oxygen
dissolving in the metal.* Continued exposure to low-pressure oxygen is followed
by adsorption of O2 molecules on metal atoms exposed through the first adsorbed
layer. Since the second layer of oxygen is bonded less energetically than the first
layer, it is adsorbed without dissociation to its atoms. The resultant structure is
usually more stable on transition than on nontransition metals [4]. Any additional
layers of adsorbed oxygen are still less strongly bonded, and the outer layers, at
*J. Moreau and J. Bénard [C. R. Acad. Sci (Paris) 242, 1724 (1956)] showed, through observation of
the metal surface in H2O–H2 mixtures at elevated temperatures, that oxygen adsorbed on an 18% Cr
stainless steel is thermodynamically more stable than the metal oxide. For analogous data on iron,
see A. Pignocco and G. Pellissier, J. Electrochem. Soc. 112, 1118 (1965); E. Hondros, Acta Metall. 16,
1377 (1968).
INITIAL STAGES 217
elevated temperatures, eventually become mobile, with the corresponding dif-

fraction pattern being that of an amorphous structure.
Because the free energy of adsorption per mole of oxygen decreases with
amount of oxygen adsorbed (the O–substrate bond becomes weaker), multilayer
adsorbed oxygen on metal M eventually favors transformation to a crystalline
stoichiometric oxide. In other words, ΔG for O·Mads + nO2 → (nO2)·O·Mads
becomes less negative per mole O2 as n increases, whereas ΔG for 2nM +
(nO2)·O·Mads → (2n + 1)MO to form the oxide becomes correspondingly more
negative. Therefore, oxide formation nucleates preferably at surface sites where
multilayer adsorption is favored, such as at surface vacancies, ledges, or other
imperfections. When conditions are favorable, oxide nuclei form at specific sites
of the surface, aided by rapid surface diffusion of M and O ions (Fig. 11.1) [5].
Because the amount of adsorbed oxygen on any likely site increases with oxygen
pressure, more sites are brought into play, and the density of nuclei increases.
Similarly, since multilayer adsorption decreases at elevated temperatures, the
density of nuclei decreases with increase of temperature [6, 7]. Nuclei grow
rapidly to a certain height on the order of nanometers,* and then they grow more
Figure 11.1. Nuclei of Cu2O formed on copper surface at 10−1 mmHg oxygen pressure
(13.3 Pa), 525 °C, 20 s (17,600×). Black lines are bands of imperfections (stacking faults) in the
copper lattice (Brockway and Rowe [5]).
*Limited perhaps by the electron tunneling distance [4] below which electrons can penetrate the
metal-oxide–interface barrier without first acquiring the usual activation energy.
218 OXIDATION
rapidly in a lateral rather than in a vertical direction. On copper exposed to

1 mm Hg (133 Pa) oxygen pressure at 550 °C, a continuous film of Cu2O forms
within 6 s; at 1 atm O2, the time required is still less.
Using transmission electron microscopy and computer modeling, it has been
shown that the metal–scale interface is very tightly bonded as a result of epitaxial
relations between the metal and the scale, at least for thin scales [8]; that is, as
the crystalline oxide grows on the metal substrate, the crystal structure of the
oxide is aligned with the structure of the metal. Growth of the resulting thin
continuous oxide film may be controlled by transfer of electrons from metal to
oxide [9], or by migration of metal ions in a strong electric field set up by nega-
tively charged oxygen adsorbed on the oxide surface [10]. When the continuous
film reaches a thickness in the order of several hundred nanometers, diffusion of
ions through the oxide may become rate controlling instead. The latter situation
prevails so long as the oxide remains continuous. Eventually, at a critical thick-
ness, the stresses set up in the oxide may cause it to crack and detach—called
spalling—and the oxidation rate increases.
11.3 THERMODYNAMICS OF OXIDATION:

FREE ENERGY–TEMPERATURE DIAGRAM
Graphical data of the standard Gibbs free energy of formation of oxides versus
temperature, shown in Fig. 11.2, can be used to predict the conditions under which
a metal is oxidized or a metal oxide is reduced [11]. For every reaction in Fig.
11.2, the reactant is 1 mole of O2, so that the reactions are
2x 2
M + O2 = M x O y
y y
The standard Gibbs free energy of formation, ΔG °, for any oxide can be read
directly off the vertical axis of the graph. For example, at 1000 °C, the standard
Gibbs free energy of formation of NiO is approximately −250 kJ for two moles
of NiO.
From the diagram, we can estimate the equilibrium values of oxygen partial
pressure, as well as CO/CO2 and H2/H2O ratios in contact with metals and their
oxides, by drawing straight lines through the points labeled O, H, and C, respec-
tively, and through the point on the metal/metal oxide line at the temperature of
interest, extrapolating to the scales of CO/CO2, H2/H2O, and pO2.
11.4 PROTECTIVE AND NONPROTECTIVE SCALES
The rate of reaction in the later stages of oxidation depends on whether the thick
film or scale remains continuous and protective as it grows, or whether it contains
cracks and pores and is relatively nonprotective. Because reaction-product films
PROTEC TIVE AND NONPROTEC TIVE SC ALES 219
Figure 11.2. Standard Gibbs free energy of formation of oxides as a function of

temperature [11]. (Reprinted with permission of ASM International®. All rights reserved.
www.asminternational.org.)
are usually brittle and lack ductility, the initiation of cracks depends in some
measure on whether the surface film is formed in tension, favoring fracture, or
in compression, favoring protection. This situation, in turn, depends on whether
the volume of reaction product is greater or less than the volume of metal from
which the product forms; that is, it depends on the Pilling–Bedworth ratio, Md/
nmD, where M is the molecular weight, D is the density of scale, m and d are the
atomic weight and density of metal, respectively, and n is the number of metal
220 OXIDATION
TABLE 11.1. Pilling–Bedworth Ratios

Metal Oxide Pilling–Bedworth Ratio
Chromium Cr2O3 2.0

Cobalt CoO 1.9
Titanium TiO2 1.8
Iron FeO 1.7
Copper CuO 1.7
Nickel NiO 1.7
Aluminum Al2O3 1.3
Magnesium MgO 0.8
Calcium CaO 0.6
Lithium Li2O 0.6
atoms in a molecular formula of scale substance (n = 2 for Al2O3) [12]. If Md/nmD

>1, a protective scale is predicted to form. On the other hand, when this ratio is
less than unity, the scale is formed in tension and tends to be nonprotective.
Table 11.1 lists the Pilling–Bedworth ratios for several metals. For calcium
and magnesium, which tend to form nonprotective oxides, the ratios are 0.64 and
0.79, respectively, whereas for aluminum and chromium, which tend to form
protective oxides, the ratios are 1.3 and 2.0, respectively. Tungsten has a ratio of
3.6, and hence, the oxide, WO3, is expected to be protective, except at high tem-
peratures (approximately >800 °C), where it volatilizes.
Although the Pilling–Bedworth ratio may be greater than 1, so that a protec-
tive scale would be predicted, at high temperatures the rapid growth of oxide
may cause compressive stresses to become so great that the scale spalls; for
example, Cr2O3 scale on pure chromium at 1100 °C, with a Pilling–Bedworth ratio
of 2.0 [13]. Similarly, thick scales of TiO2 on titanium are nonprotective. Typically,
oxide is protective during the early stages of oxidation, but it becomes nonprotec-
tive above a certain thickness.
In addition to the Pilling–Bedworth ratio, protection by an oxide depends on
adherence of the oxide to the substrate, low vapor pressure and high melting
temperature of the oxide, slow oxide growth rate, and high thermodynamic stabil-
ity. The growth mechanism of the oxide is also relevant to oxide protection. For
example, if the scale forms at the metal–oxide interface by migration of oxide
ions, then compressive stresses can develop because of the constrained space
available for the oxide to occupy. On the other hand, scale that forms at the
oxide–gas interface by migration of metal ions outward is not constrained to
occupy the volume of the metal that was oxidized. Under these conditions, pro-
tective scales are expected.
11.4.1 Three Equations of Oxidation

The three main equations that express thickness y of film or scale forming on any
metal within time t are (1) the linear, (2) the parabolic, and (3) the logarithmic.
PROTEC TIVE AND NONPROTEC TIVE SC ALES 221
Figure 11.3. Equations expressing growth of film thickness, y, as a function of time of oxida-
tion, t.
The particular equation that applies depends, in part, on the ratio Md/nmD and
the relative thickness of the film or scale.
For the linear equation, the rate of oxidation is constant, or dy/dt = k and y =
kt + const, where k is a constant. Hence, the thickness of scale, y, plotted with time,
t, is linear (Fig. 11.3). This equation holds whenever the reaction rate is constant at
an interface, as, for example, when the environment reaches the metal surface
through cracks or pores in the reaction-product scale. Hence, for such metals, the
ratio Md/nmD is usually less than unity. In special cases, the linear equation may
also hold even though the latter ratio is greater than unity, such as when the con-
trolling reaction rate is constant at an inner or outer phase boundary of the reac-
tion-product scale; for example, tungsten first oxidizes at 700–1000 °C, in accord
with the parabolic equation, forming an outer porous WO3 layer and an inner
compact oxide scale [14]. When the rate of formation of the outer scale becomes
equal to that of the inner scale, the linear equation is obeyed.
For the parabolic equation, the diffusion of ions or migration of electrons
through the scale is controlling, and the rate, therefore, is inversely proportional
to scale thickness.
dy k ′
= or y2 = 2k ′t + const
dt y
222 OXIDATION
Accordingly, if y2 is plotted with t, a linear relation is obtained (Fig. 11.3). This

equation holds for protective scales corresponding to Md/nmD > 1 and is appli-
cable to the oxidation of many metals at elevated temperatures, such as copper,
nickel, iron, chromium, and cobalt.
For relatively thin protective films, as when metals oxidize initially or when
oxidation occurs at low temperatures, it is found that
dy k ′′
dt
=
t
or y = k ′′ ln ( const
t
+ 1)
This is called the logarithmic equation. Correspondingly, if y is plotted with log

(t + const), or with log t for t >> const, a linear relation is obtained. First reported
by Tammann and Köster [15], the logarithmic equation has been found to express
the initial oxidation behavior of many metals, including Cu, Fe, Zn, Ni, Pb, Cd,
Sn, Mn, Al, Ti, and Ta. The logarithmic equation can be derived on the condition
that the oxidation rate is controlled by transfer of electrons from metal to reac-
tion-product film [9] when the latter is electrically charged—that is, when it con-
tains a space charge throughout its volume. The preponderance of electric charge
of usually negative sign in oxides near the metal surface, similar to the electrical
double layer in aqueous electrolytes, has been demonstrated experimentally.
Therefore, any factor changing the work function of the metal (energy required
to extract an electron), such as grain orientation, lattice transition, or magnetic
transition (Curie temperature), changes the oxidation rate, as has been observed
[16]. When the thickness of the film exceeds the maximum thickness of the space-
charge layer, diffusion or migration through the film then usually becomes con-
trolling, the parabolic equation applies, and the factors just mentioned, such as
grain orientation and Curie temperature, no longer affect the rate. On this basis,
metals forming protective films first follow the logarithmic equation and then the
parabolic (or linear) equation.
If, for thin-film behavior, migration of ions controls the rate, and the prevail-
ing electric field within the film is considered to be set up by gaseous ions
adsorbed on the outer surface, the rate of ion migration is an exponential func-
tion of the field strength, and the inverse logarithmic equation [10] results:
1
= const − k ln t
y
This relation has been reported to hold for copper and iron oxidized at low tem-
peratures [17]. It is often difficult to distinguish between the logarithmic and the
inverse logarithmic equations because of the limited range of time over which
data can be accumulated for thin-film behavior, with either equation apparently
applying equally well. This situation also makes it difficult to evaluate other types
of equations that have been proposed, such as the cubic equation, y3 = kt + const.
Data obeying this equation can also be represented, in many cases, by a two-stage
logarithmic equation where an initial lower rate is followed by a final higher rate
WAGNER THEORY OF OXIDATION 223
[16] (Fig. 11.3). The higher rate is ascribed to formation of a diffuse space-charge
layer overlying an initially constant charge-density layer [9].
The oxidation rate for thin- or thick-film conditions increases with tempera-
ture, obeying the Arrhenius equation
reaction − rate constant = A exp ( −RTΔE ′ )

where ΔE′ is the activation energy, R is the gas constant, T is the absolute tem-
perature, and A is a constant.
11.5 WAGNER THEORY OF OXIDATION
When certain metals, such as copper, zinc, and nickel, oxidize, it is found that
metal ions migrate through the oxide to the outer oxide surface, reacting there
with oxygen. For these metals, outward diffusion of metal ions occurs in prefer-
ence to diffusion of the larger oxygen ions inward. Reaction occurring at the
outer rather than the inner oxide surface was first reported by Pfeil [18], who
noticed that when an iron surface was painted with a slurry of Cr2O3, the green-
colored layer, after oxidation, was buried in the middle or lower layers of iron
oxide. Iron ions, in other words, diffused through the Cr2O3 marker and reacted
with oxygen at the gas–oxide interface. Similarly, Wagner [19] showed, by quan-
titative studies, that Ag+ ions, and not S2− ions, migrate through Ag2S. By placing
two weighed pellets of Ag2S over silver, on top of which was molten sulfur
(Fig. 11.4), he showed that, after 1 h at 220 °C, the bottom pellet, next to the silver,
neither gained nor lost weight, whereas the top pellet, in contact with the sulfur,
gained weight chemically equivalent to the loss in weight of metallic silver.
Wagner also showed that by assuming independent migration of Ag+ and elec-
trons, the observed reaction rate could be calculated from independent physical
chemical data. He [20] derived an expression for the parabolic rate constant that
has the following simplified version [21]:
Figure 11.4. Formation of silver sulfide from silver and liquid sulfur, 1-h test, 220 °C (Wagner
[19]).
224 OXIDATION
En3 (n1 + n2 )κ
k= (11.1)
F
where E is the emf of the operating cell derived either from potential measure-
ment or free-energy data; n1, n2, and n3 are the mean cation, anion, and electron
transference numbers, respectively, within the reaction-product film; κ is the
mean specific conductivity of film substance; and F is the Faraday. The constant,
k, appears in the relation
dw A
=k
dt y
where dw/dt is the rate of formation of film substance in equivalents/second, A

is the area, and y is the thickness. The calculated value of k for silver reacting
with sulfur at 220 °C is 2–4 × 10−6 compared to the observed value of 1.6 × 10−6 eq/
cm-s. For copper oxidizing at 1000 °C and 100-mm oxygen pressure (1.3 × 104 Pa),
the calculated and observed values of k are 6 × 10−9 and 7 × 10−9 eq/cm-s, respec-
tively. The excellent agreement between theory and observation confirms the
validity of the model suggested by Wagner for the oxidation process within the
region for which the parabolic equation applies.
Equation (11.1) holds for diffusion of either cations or anions or both in the
reaction-product scale. Some metals—for example, titanium and zirconium—
oxidize, in part, by migration of oxygen ions, O2−, via anion vacancies in the cor-
responding outer oxides.
11.6 OXIDE PROPERTIES AND OXIDATION
Metal oxides are commonly in the class of electrical conductors called semicon-
ductors; that is, their conductivity lies between insulators and metallic conductors.
Conductivity increases with a slight shift from stoichiometric proportions of
metal and oxygen and with an increase of temperature. There are two types of
semiconducting oxides, namely, p- and n-types (p = positive carrier, n = negative
carrier). In the p-type, shift of stoichiometric proportions takes the form of a
certain number of missing metal ions in the oxide lattice called cation vacancies,
represented by 䊐. At the same time, to maintain electrical neutrality, an equiva-
lent number of positive holes, ⊕, form—that is, sites where electrons are missing.
A cupric ion, Cu2+, in a Cu2O lattice is an example of a positive hole. Oxides of
p-type are Cu2O, NiO, FeO, CoO, Bi2O3, and Cr2O3. A model for the Cu2O lattice
is shown in Fig. 11.5. During the oxidation of copper, cation vacancies and
positive holes are formed at the outer O2–oxide surface. These migrate to the
metal surface, a process that is equivalent to the reverse migration of Cu+ and
electrons.
For n-type oxides, excess metal ions exist in interstitial positions of the oxide
lattice, and it is these, together with electrons, that migrate during oxidation
OXIDE PROPERTIES AND OXIDATION 225
Figure 11.5. Lattice defects.
(Fig. 11.5) to the outer oxide surface. Examples of n-type oxides are ZnO, CdO,
TiO2, and Al2O3. Wagner showed that the law of mass action can be applied to
the concentration of interstitial ions and electrons, and also to cation vacancies
and positive holes. Hence, for Cu2O, the equilibrium relations are
1 ⎯
→ Cu 2O + 2Cu− + 2 ⊕
O2 ←
⎯ (11.2)
2
and
− ⋅ C ⊕ = const ⋅ pO2
2 2 1/ 2
C Cu (11.3)

For ZnO, the corresponding equilibrium is
→ Zn 2int+ + 2e − + 1 O2
⎯
ZnO ←
⎯ (11.4)
2
and
const
C Zn2+ ⋅ C e2− = (11.5)
int pO1/22
These relations lead to predictions regarding the effect of impurities in the oxide
lattice on oxidation rate; for example, if a few singly charged Li+ ions are substi-
tuted for doubly charged Ni2+ ions in the NiO lattice, the concentration of positive
holes must increase in order to maintain electrical neutrality. Hence, to maintain
equilibrium for the reaction
226 OXIDATION
1 ⎯
→ NiO + Ni2− + 2 ⊕
O2 ←
⎯
2
as expressed by
C Ni2− ⋅ C ⊕2 = const ⋅ p1O/22
the concentration of cation vacancies must decrease. This is accompanied by a

decrease in oxidation rate [22] because the rate is controlled by migration of
cation vacancies. On the other hand, if small amounts of Cr3+ are added to NiO,
the concentration of positive holes decreases, the concentration of cation vacan-
cies correspondingly increases, and the oxidation rate increases. Data of Wagner
and Zimens [23] showing the effect of alloyed chromium on oxidation of nickel
are given in Table 11.2.
At 10% Cr, the rate decreases again, possibly because a scale composed of
Cr2O3 forms instead of NiO, which alters the rate of ion migration apart from
factors described previously.
In a sulfur atmosphere, for reasons paralleling those pertaining in the situa-
tion with O2, up to 2% Cr alloyed with nickel accelerates reaction at 600–900 °C
[24]. Outward diffusion of Ni2+ occurs through cation vacancies in Ni1−xS, where
x connotes a number between 0 and 1, and incorporation of Cr3+ increases cation
vacancy concentration. In Cr–Ni alloys containing >40% Cr, outward diffusion
of Cr3+ occurs in a scale composed of Cr2S3. Incorporation of Ni2+ ions into the
Cr2S3 scale decreases cation vacancy concentration, thereby decreasing the reac-
tion rate to a value below that for pure chromium. At intermediate chromium
compositions, the scale is heterogeneous, consisting of both nickel and chromium
sulfides, with the rate of sulfidation being less than that of pure chromium for
Cr–Ni alloys containing >20% Cr.
From Eq. (11.3), it is apparent that higher partial pressures of oxygen for p-
type semiconductors must be accompanied by higher concentrations of vacancies
and holes at the O2–oxide interface. Hence, copper oxidizes at higher rates the
higher the oxygen pressure, in accord with prediction [25].
TABLE 11.2. Oxidation of Nickel Alloyed with Chromium,

1000 °C, 1 atm O2
Weight Percent Cr Parabolic Rate Constant,
k (g2cm−4s−1)
0 3.1 × 10−10
0.3 14 × 10−10
1.0 26 × 10−10
3.0 31 × 10−10
10.0 1.5 × 10−10
GALVANIC EFFEC TS AND ELEC TROLYSIS OF OXIDES 227
TABLE 11.3. Oxidation of Zinc, 390 °C, 1 atmO2

Parabolic Rate Constant,
k (g2cm−4h−1)
Zn pure 0.8 × 10−9

Zn + 0.1% Al 1 × 10−11
Zn + 0.4% Li 2 × 10−7
If small amounts of Li+ are added to ZnO, which is an n-type semiconductor,

the electron concentration decreases in order to preserve neutrality, and the
concentration of interstitial zinc ions increases in accord with the law of mass
action [Eq. (11.5)]. This increase in concentration facilitates the diffusion of
ZN 2+ +
int ; hence, Li increases the oxidation rate of zinc, contrary to its effect in NiO.
By similar reasoning, Al3+ decreases the rate. Data showing these effects are
presented in Table 11.3 [26]. The oxidation rate of zinc is almost independent of
oxygen pressure because the concentration of interstitial zinc ions is already low
at the O2–oxide interface, and any further decrease brought about by increasing
oxygen pressure has little effect on their concentration gradient referred to the
metal surface where ZN 2+ int concentration is highest.
Therefore, traces of impurities, which play a major role in semiconductor
properties, also appreciably affect rates of oxidation of metals protected by semi-
conductor films. On the other hand, alloying elements present in large percent-
ages (e.g., >10% Cr–Ni) affect the oxidation rate by a gross alteration of the
actual composition and structure of the film in addition to any effects on semi-
conducting properties.
11.7 GALVANIC EFFECTS AND ELECTROLYSIS OF OXIDES
The electrochemical nature of oxidation at elevated temperatures suggests that

galvanic coupling of dissimilar metals should affect the rate, and, in fact, such
effects do occur [27]. The reaction of silver with gaseous iodine at 174 °C, for
example, is accelerated by contact of the silver with tantalum, platinum, or graph-
ite. AgI, which is mainly an ionic conductor, forms on silver at a rate limited by
transport of electrons across the AgI layer. When silver is coupled to tantalum,
Ag+ ions diffuse over the surface of the tantalum, with the latter supplying elec-
trons that hasten conversion of silver to AgI. In addition, therefore, to the usual
film of AgI on the silver, the compound spreads progressively over the tantalum
surface (Fig. 11.6). Analogously, it was found [28] that, when silver coated with a
porous gold electroplate is exposed to sulfur vapor at 60 °C, Ag2S forms a tightly
adherent coating over the gold surface.
A second example is given by nickel completely immersed in molten Na–K
borax to a depth of about 3 mm at 780 °C in 1 atm O2 (Fig. 11.7). The rate of
228 OXIDATION
Figure 11.6. Effect of coupling tantalum to silver on reaction of iodine vapor with silver
(Ilschner-Gensch and Wagner [27]).
Figure 11.7. Galvanic cell—Pt; O2, borate melt; Ni—illustrating accelerated oxidation of
nickel through contact with platinum.
oxidation under these conditions is low because of limited access of oxygen from
the gaseous phase. If nickel is coupled to platinum or silver gauze, the latter
reaching above the liquid borax surface, corrosion of the nickel is accelerated by
a factor of 35–175 for 1-h exposure. Nickel under these conditions corrodes even
more rapidly than if exposed to pure oxygen at the same temperature because a
protective NiO scale does not form. Instead, Ni2+ dissolves in the borax electro-
lyte, and the platinum acts as an oxygen electrode; the open-circuit potential dif-
ference between platinum and nickel is 0.7 V under the conditions cited previously.
Addition of 1% FeO to borax increases the oxidation rate still more, probably
by supplying Fe2+ ions, which are oxidized to Fe3+ by oxygen near the electrolyte
surface, with the trivalent ions then being reduced again either at the cathode or
by local cell action at the nickel anode.
The dependence of oxidation on ion migration within a reaction-product
layer suggests that the oxidation rate should be affected by an applied electric
current. This was first shown to be the case by Schein et al. [29] By wrapping a
platinum wire around oxidized iron and passing a current of 1.5 A/cm2, these
investigators decreased the oxidation rate at 880 °C when iron was made cathodic,
and they accelerated the rate when iron was made anodic. Similar relations were
shown by Jorgensen for the oxidation of zinc in oxygen at 375 °C [30].
HOT CORROSION 229
11.8 HOT ASH CORROSION
An 8% Al–Cu alloy, oxidizing in air at 750 °C in the presence of MoO3 vapor

from an adjoining molybdenum wire not in contact, was found to react at an
abnormally high rate [31]. Similar accelerated oxidation in air was reported for
stainless steels containing a few percent molybdenum or vanadium [32], or as
little as 0.04% boron [33]. The oxidation products were voluminous and
porous.
An analogous accelerated damage is found in boiler tubes or gas turbine
blades operating at high temperatures in contact with combustion gases of crude
oils high in vanadium [34]. High-vanadium oils are found only in certain wells,
some of which are located in South America. The vanadium is present in the oil
as a soluble organic complex and, hence, is not easily removed. The solid residual
ash of such oils may reach 65% V2O5 or higher, and the damage caused by the
ash is not different from that observed when vanadium is alloyed with heat-
resistant materials.
Damage of this kind is sometimes called catastrophic or accelerated oxida-
tion, or hot ash corrosion [35]. It has been suggested that the cause is a low-
melting oxide phase that acts as a flux to dislodge or dissolve the protective scale.
The melting points of V2O5, MoO3, and B2O3, for example, are 658 °C, 795 °C, and
294 °C, respectively, compared to 1527 °C for Fe3O4. Eutectic combinations of
oxides reduce the melting point still further. In the case of vanadium-containing
oils, the presence of sulfur and sodium compounds in the oil and the catalytic
effect of V2O5 for converting SO2 to SO3 result in a scale containing Na2SO4 and
various metal oxides, the melting point of which has been found to be as low
as 500 °C. Additions to oil of substances (e.g., calcium or magnesium soaps,
powdered dolomite, or powered Mg) that raise the melting point of the ash by
forming CaO (m.p. 2570 °C) or MgO (m.p. 2800 °C) are found, accordingly, to be
beneficial. Also, operating at temperatures below the melting point of the liquid
phase avoids catastrophic oxidation. Similarly, alloys high in nickel are more
resistant because of the high melting point of NiO (1990 °C).
11.9 HOT CORROSION
Hot corrosion is the accelerated oxidation of a material at elevated temperatures

induced by a thin film of fused salt deposit [36]. It is called ‘hot corrosion’ because,
being caused by a thin electrolyte film, it shares some similarities with aqueous
atmospheric corrosion, in which corrosion is commonly controlled by the diffu-
sion of oxygen to the metal surface. In hot corrosion, the soluble oxidant is SO3
( S2 O72− ) in the fused salt.
In the late 1960s, during the Viet Nam conflict, hot corrosion caused severe
corrosion of gas turbine engines of military aircraft during operation over sea-
water. Sulfide formation results from the reaction of the metallic substrate with
a thin film of fused salt of sodium sulfate. The condensed liquid film deposits
230 OXIDATION
either by chemical deposition (i.e., the vapor pressure of Na2SO4 in the vapor
phase exceeds its equilibrium partial pressure at the substrate temperature) or
by physical deposition (solid or liquid salt detaches from an upstream component
and attaches to a hot substrate on impact) [36]. In metallographically examining
corroded components, oxide particles were observed to be dispersed in the adher-
ent salt film. As a result, a fluxing mechanism may apply, in which an otherwise
protective oxide scale on the substrate surface dissolves at the oxide/salt
interface, but precipitates as non-protective particles within the salt film [36].
The fluxing mechanism of hot corrosion has been thoroughly reviewed by
Rapp [36].
Hot corrosion may occur in the absence of metallic contaminants in the fuel.
It was first identified in marine propulsion gas turbines where service temperatures
of first-stage blades and vanes were in the range 650–700 °C (1200–1300 °F). The
accelerated attack was repeated in the laboratory [37] by applying a thin coating
of Na2SO4 to either 30% Cr–Co or 30% Cr–Ni alloys and oxidizing at 600–900 °C
(1110–1650 °F) in O2 at 1 atm containing 0.15% (SO2 + SO3). The highest oxidation
rates occurred at 650–750 °C, in accord with practical experience. Oxidation pro-
ducts consisted mostly of once-liquid mixtures of Na2SO4 + CoSO4 (or NiSO4).
Metallic sulfides often form inclusions or a network of sulfides along grain bound-
aries of the alloy; the corresponding attack is then called sulfidation.
It has been suggested that lower oxidation rates above 750 °C result from
formation of protective Cr2O3 films unable to form at lower temperatures; e.g.,
at 650 °C [37]. In turn, the presence of Cr2O3 films may be related to the increased
volatility and lesser tendency of Na2SO4 to deposit on the alloy surface at higher
temperatures [38, 39].
Damaging deposits of Na2SO4 may originate alone from sea salt contamina-
tion of intake air. Sulfur dioxide and trioxide of oil combustion products also
contribute, but hot corrosion of marine turbine blades may occur even with use
of very low-sulfur fuels [38]. High-chromium alloys are more resistant to hot
corrosion than are low-chromium alloys.
Ilschner-Gensch and Wagner suggested [27] that the mechanism is not one of
melting point or fluxing alone, but may also involve galvanic effects. A spongy,
porous network of an electronically conducting oxide, such as Fe3O4 filled with a
liquid electrolyte, reproduces the cell described previously containing a platinum
cathode and a nickel anode in contact with molten borax. The Fe3O4 sponge acts
as an oxygen electrode of large area, and the base metal acts as an anode. Supplied
with a liquid electrolyte in which oxygen and metal ions migrate rapidly, such a cell
accounts for an accelerated oxidation process far exceeding the rate for a metal
reacting directly with gaseous oxygen through a continuous oxide scale.
11.10 OXIDATION OF COPPER
Copper oxidizes in air at low temperatures (<260 °C) in accord with the two-stage
logarithmic equation, forming a film of Cu2O. The rate varies with crystal face,
OXIDATION OF COPPER 231
decreasing in the order (100) > (111) > (110). Heat treatment of polycrystalline
copper with hydrogen at 300–450 °C decreases the oxidation rate in oxygen at
200 °C because submicroscopic surface facets are formed by adsorbed hydrogen,
presumably favoring the (111) orientation. On the other hand, heat treatment
with nitrogen or helium increases the rate because adsorbed oxygen (traces from
gas or metal) favors submicroscopic facets of predominantly (100) orientation
[40].
Between about 260 °C and 1025 °C, the Cu2O film is overlaid by a superficial
film of CuO. Oxidation changes from logarithmic to parabolic behavior above
400–500 °C. Only Cu2O forms in air above 1025 °C. Copper oxidizes at a rate
slightly higher than that for iron, and much more rapidly than that for nickel or
the heat-resistant Cr–Fe alloys. This is shown by the following temperatures [41],
below which the scaling losses in air are less than approximately 2–4 g m−2h−1: Cu,
450 °C; Fe, 500 °C; Ni, 800 °C; 8–10% Cr–Fe (0.1% C), 750 °C; 25–30% Cr–Fe
(0.1% C), 1050–1100 °C.
Alloying elements that are particularly effective for improving oxidation
resistance at high temperatures are aluminum, beryllium, and magnesium; for
example, at 256 °C, a 2% Be–Cu alloy oxidizes in 1 h at 1/14 the rate of copper
[42]. Maximum improvement by aluminum additions occurs at about 8% [43].
11.10.1 Internal Oxidation

When alloyed with small percentages of certain metals (e.g., aluminum, beryllium,
iron, silicon, manganese, tin, titanium, and zinc), copper oxidizes with precipita-
tion of oxide particles within the body of the metal as well as forming an outer
oxide scale. Oxidation within the metal is called subscale formation or internal
oxidation. Similar behavior is found for many silver alloys, but without formation
of an outer scale. Internal oxidation is not observed, in general, with cadmium-,
lead-, tin-, or zinc-based alloys. A few exceptions have been noted, such as for
alloys of sodium–lead, aluminum–tin, and magnesium–tin [44]. Internal oxidation
is usually not pronounced for any of the iron alloys.
The mechanism is apparently one of oxygen diffusing into the alloy and
reacting with alloying componens of higher oxygen affinity than that of the base
metal before the alloying components can diffuse to the surface. Above a critical
concentration of the alloying component, a compact protective layer of the
component oxide tends to be formed at the external surface which thereafter
suppresses internal oxidation. In accord with a diffusion-controlled mechanism,
the depth of subscale grows in accord with the parabolic equation [44]. The
subject was reviewed by Rapp [45].
11.10.2 Reaction with Hydrogen (“Hydrogen Disease”)

The tendency of copper to dissolve oxygen when the metal is heated in air leads
to rupture of the metal along grain boundaries by formation of steam when the
metal is subsequently heated in hydrogen. Cast tough-pitch copper containing
232 OXIDATION
free Cu2O is very sensitive to this type of damage. Instances are on record where
damage has been caused by hydrogen at temperatures as low as 400 °C (750 °F).
Oxygen-free coppers are not susceptible, but they may become moderately so,
however, should they be heated at any time in oxygen or in air.
Silver similarly dissolves oxygen when heated at elevated temperatures in
air, and it becomes blistered or loses ductility if later heated in hydrogen above
500 °C (925 °F). The mechanism is the same as that applying to copper. Oxygen-
free silver heated in hydrogen for 1 h at 850 °C (1550 °F) is not embrittled or
damaged. However, when it is heated immediately afterward in air at the same
temperature, loss of ductility occurs that is similar to, but not as severe as, the
characteristic loss when silver containing oxygen is heated in hydrogen [46]. Some
dissolved hydrogen undoubtedly escapes before oxygen can diffuse into the
silver, hence diminishing subsequent damage. Gold and platinum dissolve little
or no oxygen and, consequently, are not subject to similar damage when heated
in hydrogen.
11.11 OXIDATION OF IRON AND IRON ALLOYS
In the low-temperature region (approx 250 °C), the oxidation rate of iron is sensi-
tive to crystal face, decreasing in the order (100) > (111) > (110) [47]. The oxide
nuclei, apparently consisting of Fe3O4, grow to form a uniform film of oxide.
Subsequently, α Fe2O3 nucleates and covers the Fe3O4 layer [48, 49].
Oxidation of iron in the parabolic range is complicated by formation of as
many as three distinct layers of iron oxide, and the proportions of these layers
change as the temperature or oxygen partial pressure changes. Data reported by
various investigators are not in good agreement, probably because of variations
in the purity of iron used for oxidation tests—particularly its carbon content.
At 600 °C in 1 atm O2 for 100 min, it is reported that the scale is composed
of two layers: an inner FeO layer equal in weight to an outer Fe3O4 layer [50]. At
900 °C for 100 min, a three-layer scale is composed of 90% FeO, 9% Fe3O4, and
less than 1% Fe2O3. Below 570 °C (1058 °F), FeO is unstable and, if any is formed
above this temperature, it decomposes at room temperature into Fe3O4 plus Fe.
The most efficient alloying elements for improving oxidation resistance of
iron in air are chromium and aluminum. Use of these elements with additional
alloyed nickel and silicon is especially effective. An 8% Al–Fe alloy is reported
to have the same oxidation resistance as a 20% Cr–80% Ni alloy [51]. Unfortu-
nately, the poor mechanical properties of aluminum–iron alloys, the sensitivity of
their protective oxide scales to damage, and the tendency to form aluminum
nitride that causes embrittlement have combined to limit their application as
oxidation-resistant materials. In combination with chromium, some of these
drawbacks of aluminum–iron alloys are overcome.
The good oxidation resistance of the chromium–iron alloys, combined with
acceptable mechanical properties and ease of fabrication, accounts for their wide
commercial application. Typical oxidation behavior is shown in Fig. 11.8.
LIFE TEST FOR OXIDATION-RESISTANT WIRES 233
Figure 11.8. Effect of alloyed chromium on oxidation of steels containing 0.5% C, 220 h
[E. Houdremont, Handbuch der Sonderstahlkunde, Vol. I, Chromstähle, Springer, Berlin (1956),
p. 815, Fig. 677]. (With kind permission of Springer Science and Business Media.)
Improvement in oxidation resistance of iron by alloying with aluminum or

chromium probably results from a marked enrichment of the innermost oxide
scale with respect to aluminum or chromium. The middle oxide scales are known,
from chemical analysis, to be so enriched, and electron-microprobe analyses
confirm marked enrichment of chromium in the oxide adjacent to the metal
phase in the case of chromium–iron alloys [52]. These inner oxides resist ion and
electron migration better than does FeO. For chromium–iron alloys, the enriched
oxide scale is accompanied by depletion of chromium in the alloy surface imme-
diately below the scale. This situation accounts for occasional rusting and other-
wise poor corrosion resistance of hot-rolled stainless steels that have not been
adequately pickled following high-temperature oxidation.
11.12 LIFE TEST FOR OXIDATION-RESISTANT WIRES
The merit of a particular alloy for resisting high-temperature environments,

especially on long exposures, depends not only on the diffusion-barrier properties
of reaction-product scales, but also on the continuing adherence of such scales
to the metal. Scales that are otherwise protective often spall (become detached)
during cooling and heating cycles because their coefficient of expansion differs
from that of the metal. Hence, an ASTM accelerated test [53] for oxidation resis-
tance of wires calls for a cyclic heating period of 2 min at a specific temperature
followed by a cooling period of 2 min. Alternate heating and cooling results in
much shorter life than would occur if the wire is heated continuously. The life of
a wire in this test is measured as the time to failure or the time to reach a 10%
234 OXIDATION
Figure 11.9. Life of heat-resistant alloy wires in ASTM life test as a function of temperature
(20% Cr–Ni and 5–26% Cr–Fe), in air of 100% relative humidity at 25 °C (Brasunas and Uhlig
[54]). (Copyright ASTM International. Reprinted with permission.)
increase in electrical resistance. An equation related to the Arrhenius reaction-

rate equation expresses the dependence of life on temperature [54]:
ΔE ′
log life(h) = + const
2.3RT
Typical test results for life of several alloys are given in Fig. 11.9. The life of the
most resistant alloys is more sensitive to temperature change (higher activation
energy ΔE′) than that of alloys with inherently shorter life.
11.13 OXIDATION-RESISTANT ALLOYS
11.13.1 Reactive Element Effect (REE)

The reactive element effect (REE) is obtained when 1 wt.% or less of a reactive
element, such as yttrium, hafnium, lanthanum, zirconium, or cerium, is added to
OXIDATION-RESISTANT ALLOYS 235
high-temperature alloys containing chromium or aluminum. The effect can be

obtained when the reactive element is added as an alloy addition or when a
coating of the reactive element oxide is applied to the surface of the alloy. The
useful life of high-temperature alloys is typically limited by spalling of the oxide
from the metal surface. Reactive elements greatly improve the spalling resistance
of both chromia-forming and alumina-forming alloys. Commercial chromia-
forming heater alloys now all contain small amounts of one or more reactive
elements, and yttrium has become a commonly used reactive element addition
to high-temperature alloys [55, 56].
Applying a 4-nm-thick coating of ceria (CeO2) or yttria (Y2O3) has been
found to increase the oxidation resistance of chromium and iron–chromium
alloys. By using secondary ion mass spectrometry (SIMS) to establish the location
of the reactive element in the oxide scale, the reactive element was found in the
middle of the oxide scale, suggesting that inward oxygen transport in chromium
oxide is the dominant transport mechanism. Addition of the reactive element
inhibits the diffusion of Cr and results in growth primarily by the inward diffusion
of oxygen [56, 57].
11.13.2 Chromium–Iron Alloys

The 4–9% Cr alloys are widely used for oxidation resistance in oil-refinery
construction. The 12% Cr–Fe alloy is used for steam turbine blades because of
excellent oxidation resistance and good physical properties. The 9–30% Cr alloys
are used for furnace parts and burners; when combined with silicon and nickel,
and sometimes other alloying elements, they are used for valves of internal-
combustion engines. The approximate upper temperature limits for exposure to
air are presented in Table 11.4.
Addition of 1% yttrium to a 25% Cr–Fe alloy was reported to extend the
upper limit of oxidation resistance to about 1375 °C (2500 °F) [58, 59]. Rare-earth
metal additions, such as yttrium, in general, are beneficial to oxidation resistance
of chromium and chromium alloys, including gas turbine alloys [60].
TABLE 11.4. Approximate Upper Temperature Limits for

Exposure of Cr–Fe Alloys to Air
% Cr in Cr–Fe Maximum Temperature in Air
Alloys
°C °F
4–6 650 1200

9 750 1375
13 750–800 1375–1475
17 850–900 1550–1650
27 1050–1100 1925–2000
236 OXIDATION
11.13.3 Chromium–Aluminum–Iron Alloys

The chromium–aluminum–iron alloys have exceptional oxidation resistance,
combining the oxidation-resistant properties imparted by chromium and alumi-
num; for example, the 30% Cr, 5% Al, 0.5% Si alloy (Trade name: Megapyr)
resists oxidation in air up to at least 1300 °C (2375 °F). Similarly, the 24% Cr,
5.5% Al, 2% Co alloy (Trade name: Kanthal A) is resistant up to 1300 °C.
They are used, among other applications, for furnace windings and parts and for
electric-resistance elements. Drawbacks in their properties are poor high-
temperature strength and tendency toward embrittlement at room temperature
after prolonged heating in air, caused in part by aluminum nitride formation. For
this reason, furnace windings must be well-supported and are usually corrugated
in order to allow for expansion and contraction.
11.13.4 Nickel and Nickel Alloys

The good oxidation resistance of nickel is improved by adding 20% Cr; this alloy
(one U.S. trade name: Nichrome V) is resistant in air to a maximum temperature
of about 1150 °C (2100 °F). It is a heat-resistant alloy that combines excellent
oxidation resistance with good physical properties at both low and elevated
temperatures. Oxidation resistance of the commercial alloy is considerably
improved by the addition of calcium metal deoxidizer during the melting process,
which is said to avoid oxidation of the alloy along grain boundaries. Small
amounts of zirconium, thorium, and rare-earth metals (e.g., cerium) are also
beneficial, probably in part because they decrease the tendency of protective
oxides to spall. This explanation was also mentioned earlier as applying to the
beneficial effect of the rare-earth yttrium when alloyed with the chromium–iron
alloys.
The 16% Cr, 7% Fe, 76% Ni alloy (Trade name: Inconel 600) is slightly less
resistant to oxidation than the 20% Cr–Ni alloy, but similarly has excellent physi-
cal properties, is readily fabricated or welded, and can be used in air up to a
maximum temperature of about 1100 °C (2000 °F). Electrical heating units for
some stoves are fabricated of this alloy in tubular form. An electric heating wire
of the 20% Cr–Ni alloy inside the tube is insulated from the outer sheath by
powdered MgO. Because of its high nickel content and good strength (nickel
does not readily form a carbide or nitride), this alloy is often used for construc-
tion of carburizing or nitriding furnaces.
Some heat-resistant thermocouple wires consist of nickel alloys. The 10%
Cr–Ni alloy (Chromel P) and 2% Al, 2% Mn, 1% Si, bal. Ni alloy (Alumel) can
be exposed to air at a maximum temperature of about 1100 °C (2000 °F).
Nickel and high-nickel alloys tend to oxidize along grain boundaries when
subject to alternate oxidation and reduction. Alloying with chromium reduces
this tendency. Also, in contact with sulfur or sulfur atmospheres at elevated tem-
peratures, nickel and high-nickel alloys are subject to intergranular attack. Con-
sequently, nickel is not usefully resistant to such atmospheres above about 315 °C
REFERENCES 237
(600 °F). For best resistance to sulfur-containing environments, iron-base alloys

should contain high chromium and low nickel.
Gas turbine blades are essentially nickel-base or cobalt-base alloys contain-
ing substantial amounts of chromium, several percent aluminum, and a few
hundredths percent yttrium. Their susceptibility to hot corrosion and sulfidation
has already been discussed. Applied coatings of aluminum or of aluminum–
chromium–yttrium increase resistance to attack.
11.13.5 Furnace Windings

Twenty percent chromium–nickel and various chromium–aluminum–iron alloys
are in common use as furnace windings. To achieve higher temperatures in air, a
10% Rh–Pt alloy can be used up to at least 1400 °C (2550 °F). This alloy performs
better than pure platinum because of higher strength and a lower rate of grain
growth. A single crystal of the same dimensions as the resistance wire cross
section tends to shear easily and cause failure.
Molybdenum-wound furnaces are operated to at least 1500 °C (2725 °F).
Because molybdenum oxidizes in air, such furnace windings are blanketed in a
protective atmosphere of hydrogen.
REFERENCES
1. C. Coddet, High temperature corrosion and protection of materials 6, Proceedings,

6th International Symposium on High Temperature Corrosion and Protection of
Materials, Les Embiez, France, May 2004, Part 1, Trans Tech Publications, Uetikon-
Zuerich, Switzerland, 2004, p. 193.
2. T. Hejwowski and A. Weronski, Vacuum 65, 427 (2002).
3. A. MacRae, Surface Sci. 1, 319 (1964).
4. H. H. Uhlig, Corros. Sci. 7, 325 (1967).
5. L. Brockway and A. Rowe, in Fundamentals of Gas–Surface Interactions, H. Saltsburg
et al., editors, Academic Press, New York, 1967. p. 147.
6. F. Gronlund, J. Chim. Phys. 53, 660 (1956).
7. J. Bénard, F. Gronlund, J. Oudar, and M. Duret, Z. Elektrochem. 63, 799 (1959).
8. Robert A. Rapp, Mater. Sci. Forum 154, 119 (1994).
9. H. H. Uhlig, Acta Metall. 4, 541 (1956).
10. N. Cabrera and N. Mott, Rep. Progr. Phys. 12, 163 (1949).
11. B. Mishra, in Metals Handbook, Desk Edition, 2nd edition, ASM International, Materi-
als Park, OH, 1998, p. 718.
12. N. Pilling and N. Bedworth, J. Inst. Metals 29, 534 (1923).
13. ASM Handbook, Vol. 13A, Corrosion: Fundamentals, Testing, and Protection, ASM
14. Per Kofstad, High-Temperature Oxidation of Metals, Wiley, New York, 1966, pp.
252–254.
238 OXIDATION
15. G. Tammann and W. Köster, Z. Anorg. Allg. Chem. 123, 196 (1922).
16. H. Uhlig, J. Pickett, and J. MacNairn, Acta Metall. 7, 111 (1959).
17. D. Gilroy and J. Mayne, Corros. Sci. 5, 55 (1965).
18. L. Pfeil, J. Iron Steel Inst. 119, 520 (1929).
19. C. Wagner, Z. Phys. Chem. 21B, 25 (1933).
20. C. Wagner, Atom Movements, American Society for Metals, Cleveland, OH, 1951, pp.
153–173; C. Wagner and K. Grünewald, Trans. Faraday Soc. 34, 851 (1938).
21. Ref. 14, pp. 113–127; T. P. Hoar and L. E. Price, Trans. Faraday Soc. 34, 867 (1938).
22. K. Hauffe and H. Pfeiffer, Z. Elektrochem., 56, 390 (1952).
23. C. Wagner and K. Zimens, Acta Chem. Scand. 1, 547 (1947).
24. S. Mrowec, T. Werber, and N. Zastawnik, Corros. Sci. 6, 47 (1966).
25. C. Wagner and K. Grünewald, Z. Phys. Chem. 40B, 455 (1938).
26. C. Gensch and K. Hauffe, Z. Phys. Chem. 196, 427 (1950).
27. C. Ilschner-Gensch and C. Wagner, J. Electrochem. Soc. 105, 198, 635 (1958).
28. T. Egan and A. Mendizza, J. Electrochem. Soc. 107, 353 (1960).
29. F. Schein, B. LeBoucher, and P. LaCombe, C. R. Acad. Sci. (Paris) 252, 4157 (1961).
30. P. Jorgensen, J. Electrochem. Soc. 110, 461 (1963).
31. G. Rathenau and J. Meijering, Metallurgia 42, 167 (1950).
32. A. Brasunas and N. Grant, Trans. Am. Soc. Metals 44, 1117 (1952).
33. A. Fry, Tech. Mitt. Krupp 1, 1 (1933).
34. F. Monkman and N. Grant, Corrosion 9, 460 (1953).
35. J. Demo, Mater. Perf. 19 (3), 9, (1980).
36. Robert A. Rapp, Corros. Sci. 44 (2), 209 (2002).
37. K. Luthra and D. Shores, J. Electrochem. Soc. 127, 2202 (1980).
38. P. Bergman, Corrosion 23, 72 (1967).
39. J. Elliott, Solid State Chemistry of Energy Conversion and Storage, J. Goodenough and
M. Whittingham, editors, Advances in Chemistry Series, No. 163, American Chemical
Society, Washington, D.C., 1977.
40. A. Swanson and H. Uhlig, J. Electrochem. Soc. 118, 1325 (1971).
41. B. Lustman, Metal Progr. November, 850 (1946).
42. W. Campbell and U. Thomas, Trans. Electrochem. Soc. 91, 623 (1947).
43. H. Nishimura, J. Min. Metall, Kyoto 9, 655 (1938).
44. F. N. Rhines et al., Trans. Am. Inst. Min. Metall. Eng. 147, 205, 318 (1942)
45. R. Rapp, Corrosion 21, 382 (1965).
46. D. Martin and E. Parker, Min. Metall. Eng. 152, 269 (1943).
47. J. Wagner, Jr., K. Lawless, and A. Gwathmey, Trans. Metall. Soc. AIME 221, 257
(1961).
48. R. Grauer and W. Feitknecht, Corros. Sci. 6, 301 (1966).
49. P. Sewell and M. Cohen, J. Electrochem. Soc. 111, 501 (1964).
50. M. Davies, M. Simnad, and C. Birchenall, J. Metals 3, 889 (1951).
51. N. Ziegler, Min. Metall. Eng. 100, 267 (1932).
52. G. Wood and D. Melford, J. Iron Steel Inst. 198, 142 (1961).
PROBLEMS 239
53. ASTM B76-90(2007), Standard Test Method for Accelerated Life of Nickel–Chromium
and Nickel–Chromium–Iron Alloys for Electrical Heating, ASTM, West Conshohocken,
PA.
54. A. deS. Brasunas and H. H. Uhlig, ASTM Bulletin, No. 182, ASTM, Philadelphia, May
1952, p. 71.
55. J. Stringer, Mater. Sci. Engi. A120, 129 (1989).
56. B. A. Pint, in John Stringer Symposium on High Temperature Corrosion, Proceedings
from Materials Solutions Conference 2001, ASM International, Materials Park, OH,
2003.
57. M. J. Graham, Corrosion 59 (6), 475 (2003).
58. J. Fox and J. McGurty, in Refractory Metals and Alloys, M. Semchyshen and J. Harwood,
editors, Interscience, New York, 1961, p. 207.
59. E. Fellen, J. Electrochem. Soc. 108, 490 (1961).
60. R. Viswanathan, Corrosion 24, 359 (1968).
GENERAL REFERENCES
N. Birks, G. H. Meier, and F. S. Pettit, Introduction to the High Temperature Oxidation of

Metals, 2nd edition, Cambridge University Press, Cambridge, U.K., 2006.
P. Kofstad, High Temperature Corrosion, Elsevier, London, 1988.
P. Kofstad, High-Temperature Oxidation of Metals, Wiley, New York, 1966.
R. B. Pond and D. A. Shifler, High-temperature corrosion-related failures, in ASM Hand-
book, Vol. 11, Failure Analysis and Prevention, ASM International, Materials Park, OH,
2002, pp. 868–880.
R. Rapp, editor, High Temperature Corrosion, National Association of Corrosion Engi-
neers, Houston, TX, 1983.
P. Steinmetz, I. G. Wright, G. Meier, A. Galerie, B. Pieraggi, and R. Podor, editors, High Tem-
perature Corrosion and Protection of Materials 6, Proceedings of the 6th International
Symposium on High Temperature Corrosion and Protection of Materials, Les Embiez,
France, May 2004, Trans Tech Publications, Uetikon-Zuerich, Switzerland, 2004.
P. F. Tortorelli, I. G. Wright, and P. Y. Hou, editors, John Stringer Symposium on High
Temperature Corrosion, Proceedings from Materials Solutions Conference 2001, ASM
International, Materials Park, OH, 2003.
Materials Science and Engineering, A120/121, November 15, 1989, Proceedings, 2nd
International Symposium on High Temperature Corrosion of Advanced Materials and
Coatings, Les Embiez, France, May 1989.
PROBLEMS
1. Calculate Md/nmD for aluminum forming Al2O3 and for sodium forming
Na2O. Indicate whether the oxides are protective.
240 OXIDATION
2. (a) Calculate the volume of FeO (d = 5.95 g/cm3) that results from the oxidation of
1 cm3 of iron.
(b) Similarly, calculate the volume of Fe3O4 (d = 5.18 g/cm3) that results from the oxi-
dation of 1 cm3 of iron.
(c) Same as above, but, for Fe2O3 (d = 5.24 g/cm3).
3. Estimate the free energy of formation of NiO at 780 °C from the cell illustrated
in Fig. 11.7 (Section 11.7). Assume that NiO in borax is saturated. Compare
with reported values as follows:
Temperature (K) ΔG ° (kJ/mole)
1000 −146.8
1100 −137.7
4. Copper oxidizes within the parabolic range at a higher rate the higher the
oxygen pressure.
(a) What is the quantitative relation [use Eq. (11.3), Section 11.6]?
(b) Make the same calculation for nickel.
5. Using the Gibbs free energy of formation versus temperature diagram,

Fig. 11.2, at 600 °C, estimate
(a) the minimum pressures of oxygen required to oxidize aluminum, chromium, and
silicon to Al2O3, Cr2O3, and SiO2;
(b) the maximum ratios of H2/H2O required to produce the oxides in (a); and
(c) the maximum ratios of CO/CO2 required to produce the oxides in (a).
Answers to Problems
1. 1.28; 0.58
2. (a) 1.7 cm3; (b) 2.1 cm3; (c) 2.1cm3
3. Calculated ΔG ° = −135 kJ/mole
4. (a) Rate is proportional to po21/8; (b) Rate is proportional to po21/6.
12
STRAY-CURRENT CORROSION
12.1 INTRODUCTION
Stray electric currents are those that follow paths other than the intended circuit,
or they may be any extraneous currents in the earth. If currents of this kind enter
a metal structure, they cause corrosion at areas where the currents leave to enter
the soil or water. Usually, natural earth currents are not important from a corro-
sion standpoint, either because their magnitude is small or because their duration
is short. Under some conditions, pipelines can incur considerable corrosion
damage as a result of telluric currents—that is, currents induced in the steel
pipeline by changes in the geomagnetic field of the earth [1].
Damage by alternating current (ac) is less than that by direct current (dc),
with the resultant corrosion usually being greater for lower frequency and less
for higher-frequency currents. Jones [2] reported that in 0.1N NaCl, the increased
corrosion rate of a carbon steel caused by a 60-cycle current density of 300 A/m2
is negligible in an aerated solution, but severalfold higher (but still low) in a
deaerated solution. This probably means that rates of reversible, or partially
reversible, anode–cathode reactions in the aerated solution are symmetrical with
respect to alternating applied potentials, whereas in the deaerated solution
the reactions are not symmetrical, largely because of the hydrogen evolution

241
242 STR AY-CURRENT CORROSION
reaction. It has been estimated that for metals like steel, lead, and copper in
common environments, 60-cycle alternating current (ac) causes less than 1% of
the damage caused by an equivalent dc current [3].
The effect of unsymmetrical reactions (Faradaic rectification) is observed
especially in the ac corrosion of metals that are passive (mostly by Definition 1,
Section 6.1). It has been reported that stainless steels subjected to ac current
electrolysis are corroded [4]; similarly, aluminum in dilute salt solutions at 15 A/
m2 (1.4 A/ft2) suffers 5%, and at 100 A/m2 (9.3 A/ft2) as much as 31% of the cor-
rosion damage caused by equivalent dc current densities. In a study of 1-V, 54-
cycle ac current superimposed on dc current, Feller and Rückert [4] found that
the passive region of potentiostatic polarization curves for nickel in 1N H2SO4
completely disappeared and that high anodic current densities persisted through-
out the noble potential region. Chin and Fu [5] found analogous behavior of mild
steel in 0.5M Na2SO4, pH 7. The passive current density increased with increasing
superimposed ac current, reaching the same order as the critical current density
(no passive region) at a 60-cycle current density of 2000 A/m2. They also found
that the corrosion potential was shifted several tenths of a volt in the active
direction by an ac current density of 500 A/m2. The Flade-potential region simul-
taneously was shifted in the active direction, but the critical current density
remained about the same. These results suggest that passivity lost during the
cathodic cycle, if not restored during the anodic cycle, can account for unexpect-
edly high corrosion rates of otherwise corrosion-resistant metals in aqueous
media or in soil.
12.2 SOURCES OF STRAY CURRENTS
Sources of dc stray currents are commonly electric railways, grounded electric dc

power lines, electric welding machines, cathodic protection systems, and electro-
plating plants. Sources of ac stray currents are usually grounded ac power lines
or currents induced in a pipeline by parallel power lines. An example of dc stray
current from an electric street railway system in which the steel rails are used for
current return to the generating station is shown in Fig. 12.1. Because of poor
Figure 12.1. Stray-current corrosion of a buried pipe.

SOURCES OF STR AY CURRENTS 243
bonding between rails, combined with poor insulation of rails to the earth, some
of the return current enters the soil and finds a low-resistance path, such as a
buried gas or water main. The owner of a household water service pipe at A
benefits by cathodic protection and experiences no corrosion difficulty; but owner
B, to the contrary, is harassed by corrosion failures because the service pipe of
his house is anodic with respect to the rails. If B coats the pipe, which is an
understandable layman’s reaction to any corrosion problem, matters are made
worse because all stray currents now leave the pipe at defects in the insulating
coating at high-current densities, accelerating penetration of the pipe. The basic
rule: Never coat the anode.
Street railways have now in large part been replaced by other forms of
transportation, but the problems of stray-current corrosion originating from
metropolitan railway transit systems continue [6]. Also, cathodically protected
structures requiring high currents, when located in the neighborhood of an unpro-
tected pipeline, can produce damage similar to that by the railway illustrated
in Fig. 12.1.
Another example of stray-current corrosion is illustrated in Fig. 12.2. A
welding motor generator located on shore with grounded dc lines to a ship under
repair can cause serious damage to the hull of the ship by current returning in
part from the welding electrodes through the ship and through the water to the
shore installation. In this case, it is better to place the generator on board ship
and bring ac power leads to the generator, since ac currents leaking to ground
cause less stray-current damage.
Current flowing long a water pipe (e.g., used as an electric ground) usually
causes no damage inside the pipe because of the high electrical conductivity of
steel or copper compared to water; for example, since the resistance of any con-
ductor per unit length equals ρ/A, where ρ is the resistivity and A is the cross-
sectional area, then the ratio of current carried by a metal pipe compared to that
carried by the water it contains is equal to ρWAM/ρMAW, where the subscripts W
and M refer to water and metal, respectively. For iron, ρM = 10−5 Ω-cm; and for a
potable water, ρW may be 104 Ω-cm. Assuming that the cross-sectional area of
water is 10 times that of the steel pipe, it is seen that if current through the pipe
is 1 A, only about 10−8 A flows through the water. This small current leaving the
Figure 12.2. Stray-current damage to a ship by a welding generator.

Figure 12.3. Effect of current flowing along a buried pipeline on corrosion near insulated
couplings.
TABLE 12.1. Weight Loss of Metals by Stray-Current

Corrosion
Metal Equivalent Weight Weight of Metal
Corroded per
Ampere-Year
Pounds Kilograms
Fe 55.85/2 20.1 9.1

Cu 63.57/2 22.8 10.4
Pb 207.2/2 74.5 33.8
Zn 65.38/2 23.6 10.7
Al 26.98/3 6.5 2.9
pipe and entering the water causes negligible corrosion. If seawater is transported
instead, with ρW = 20 Ω-cm, the ratio of currents is 2 × 105, indicating that, even
in this case, most of the current is carried by the metallic pipe and there is very
little stray-current corrosion on the inner surface. However, where such currents
leave the pipe and enter the soil, stray-current corrosion of the outer surface may
be appreciable.
If insulating joints are installed in the above-mentioned pipe in order to
reduce stray-current pickup, corrosion is now focused on the water side of the
joint where any current that persists leaves the pipe to enter the water. Or, if a
high-resistance joint exists between two sections of a buried pipe, corrosion may
be more pronounced on the side where current enters the soil (Fig. 12.3).
12.3 QUANTITATIVE DAMAGE BY STRAY CURRENTS
In general, the amount of metal corroding at anodic areas because of stray

current can be calculated using Faraday’s law. Weight losses of typical metals for
the equivalent of 1 A flowing for one year are listed in Table 12.1.
At low current densities, local-action corrosion supplements stray-current
corrosion. At high current densities in some environments, oxygen may be
evolved, reducing the amount of metal corroding per faraday of electricity.
DETECTION OF STR AY CURRENTS 245
Amphoteric metals (e.g., lead, aluminum, tin, zinc) corrode in alkalies as well
as in acids and, hence, may be damaged at cathodic areas where alkalies accu-
mulate by electrolysis. This damage is in addition to damage at anodic areas. The
amount of cathodic corrosion is not readily estimated. Plumbites (NaHPbO2),
aluminates (NaH2AlO3), stannates (Na2SnO3), and zincates (Na2ZnO2), which are
all soluble in excess alkali, form in variable amounts per faraday, depending on
diffusion rates, temperature, and other factors. Formulas for such compounds may
also vary with conditions of formation. In general, the compounds hydrolyze at
lower values of pH some distance away from the cathode to form insoluble metal
oxides or hydroxides.
12.4 DETECTION OF STRAY CURRENTS
Stray currents may fluctuate over short or long intervals of time parallel to the
varying load of the power source. This is in contrast to galvanic or cathodic pro-
tection currents, which are relatively steady. Hence, by recording the potential of
a corroding system with respect to a reference electrode over a 24-h period, stray
currents can often be detected and their origin can be traced to the generator
source for which the load, day or night, varies in a pattern similar to that of the
measured potential change. Thus, if stray currents, as indicated by potential mea-
surements, are larger at 7 to 9 a.m. and again at 4 to 6 p.m., a street railway is
suspected. If interference by a cathodic protection system is suspected, the pro-
tective current can be turned off and on briefly at regular intervals, observing
whether the potential of the corroded structure also fluctuates at the same
frequency.
The magnitude of current leaving (or entering) a buried pipe from whatever
source can be calculated by measuring the potential difference between a posi-
tion on the soil surface directly over the pipe and a position on the soil surface
some distance away and at right angles to the pipe. If Δφ is the measured potential
difference, ρ the resistivity of soil, h the depth of pipe below the surface, and y
the distance along the soil surface over which the potential difference is mea-
sured, we obtain
ρj y2 + h2
Δφ = ln (12.1)
2π h2
where j is the total current entering or leaving the pipe surface per unit length
(for derivation, see Appendix, Section 29.5). If y is chosen equal to 10h, we
have
Δφ = 0.734ρj (12.2)
An outer reference electrode (+) with respect to a (−) reference electrode directly
over the pipe corresponds to current entering the pipe.
Figure 12.4. Four-electrode method for measuring soil resistivity.
12.5 SOIL-RESISTIVITY MEASUREMENT
The resistivity of a soil can be measured by the four-electrode method with each
electrode arranged in a straight line and each separated by the distance a (Fig.
12.4). Steady current I from a battery is passed through the two outer metal
electrodes, and the potential difference, Δφ, of the two inner reference electrodes
(e.g., Cu−CuSO4) is measured simultaneously. The measurement is usually
repeated with current direction reversed in order to cancel out any stray currents.
Then
2 πaΔφ
ρ= (12.3)
I
where ρ is the resistivity of a uniform soil measured to an approximate depth

equal to a (for derivation, see Appendix, Section 29.6).
12.6 MEANS FOR REDUCING STRAY-CURRENT CORROSION
1. Bonding. In Fig. 12.1, stray-current corrosion is completely avoided by

placing a low-resistance metallic conductor between service pipe B and
the rails at C. This is called bonding the rail and pipe systems. In the event
of a cathodic protection system causing the damage, the bond may include
a resistor just sufficient to avoid large change of potential of the unpro-
tected system when the cathodic protection current is turned on and off.
The resistor avoids major damage to the unprotected system. At the same
time, it avoids the necessity of a large increase in protective current caused
by current flowing through the bond, which in effect serves to protect the
adjoining system in addition to the protected structure. If stray currents
for some reason should periodically reverse direction, rectifying units
(diodes) are inserted into the bonding connection, thereby ensuring that
any current flow is in that direction that is nondamaging to the
structure.
PROBLEMS 247
2. Intentional Anodes and Cathodic Protection. If a bond from B to C in Fig.

12.1 is not feasible, an intentional anode of scrap iron may be buried in
the direction of the rails and attached by a copper conductor to point B.
Stray currents then cause corrosion only of the intentional anode, which
is easily replaced at low cost. If a source of dc current is inserted between
the intentional anode and the pipe such that current flows in the soil in a
direction opposite to that of the stray current, the arrangement is equiva-
lent to cathodically protecting the pipe. Cathodic protection is installed
whenever the intentional anode is not sufficient to overcome all corrosion
caused by stray currents.
3. Insulating Couplings. By installing one or more insulating couplings, the
pipeline in Fig. 12.1 becomes a less favorable path for stray currents. Such
couplings are often useful for minimizing stray-current damage. They are
less useful if voltages are so large that current is induced to flow around
the insulating joint, causing corrosion as depicted in Fig. 12.3.
REFERENCES
1. D. H. Boteler and W. H. Seager, Corrosion 54(9), 751 (1998).

2. D. Jones, Corrosion 34, 428 (1978).
3. F. Hewes, Mater. Prot. 8(9), 67 (1969).
4. H. Feller and J. Rückert, Z. Metallk. 58, 635 (1967).
5. D. Chin and T. Fu, Corrosion 35, 514 (1979).
6. G. Kish, Mater. Perf. 20 (9), 27 (Sept. 1981).
GENERAL REFERENCES
J. H. Fitzgerald III, Stray current analysis, in Uhlig’s Corrosion Handbook, 2nd edition,
Michael J. Szeliga, Stray current corrosion, in Peabody’s Control of Pipeline Corrosion,
2nd edition, R. L. Bianchetti, editor, NACE International, Houston, Texas, 2001,
pp. 211–236.
M. J. Szeliga, editor, Stray Current Corrosion: The Past, Present and Future of Rail Transit
Systems, NACE International, Houston, TX, 1994.
PROBLEMS
1. (a) A direct current of 10 A enters and leaves a steel water pipe of 2-in. outside
diameter and 0.25-in. wall thickness, containing water with resistivity of
104 Ω-cm. Calculate the current carried by the steel and that carried by the
water. Assume that the resistivity of the pipe equals 10−5 Ω-cm.
(b) Similarly, calculate the current if the pipe conveys seawater of resistivity
20 Ω-cm.
2. (a) A direct current of 10 A passes through external clamps 2 m apart attached
to a copper pipe of 5-cm outside diameter containing water of conductivity
10−4 Ω−1 cm−1. If the pipe wall thickness is 0.35 cm, calculate the total weight
of the copper in grams per year that corrodes internally at the positive
clamp because of this current.
(b) Similarly, calculate the total weight if the pipe contains seawater of con-
ductivity equal to 0.05 Ω−1 cm−1.
(c) What weight of copper would in theory corrode in one year if an insulating
joint were inserted between the clamps?
3. A long pipeline of 8-in. diameter is buried 6 ft underground. The potential
difference between two Cu−CuSO4 reference electrodes located on the soil
surface over the pipe and a point at right angles 60 ft distant, is 1.25 V. The
electrode over the pipe is negative to the other, and soil resistivity measures
3000 Ω-cm.
(a) Does current flow from or to the pipe? How many amperes per linear foot
of pipe?
(b) What is the percent error in calculated current if it is found later that the
pipe is buried 7 ft instead of 6 ft below the surface?
4. Assuming that a pipe is buried h meters underground in soil with a resistivity
of 3000 Ω-cm, plot ΔE versus y for a constant current, j, entering the pipe per
linear length of pipe in meters.
5. In measuring resistivity by the four-electrode method, what distance

between electrodes must be specified in order to apply the simplified
formula:
1000Δφ
ρ=
I
6. A stray current of 0.7 A leaves a section of buried steel pipe 2 in. in

diameter and 2 ft long. What is the initial corrosion rate in ipy caused by this
current?
7. (a) If a spherical electrode of radius a is half-buried in earth of resistivity σ,

what is the resistance R to earth as a function of distance D from the
electrode center?
(b) At what distance is the resistance within 99% of maximum?
PROBLEMS 249
Answers to Problems
2. (a) 5.0 × 10−5; (b) 0.025; (c) 1.04 × 105 g.
3. (a) 0.0173 A/ft.
(b) 6.4%.
5. 1.59 m (5.22 ft).
6. 0.33 ipy.
7. (a) R = (
σ 1 1
2π a D
− ); (b) 100a.
13
CATHODIC PROTECTION
13.1 INTRODUCTION
Cathodic protection is probably the most important of all approaches to corro-

sion control. Using an externally applied electric current, corrosion is reduced
essentially to zero. A metal surface that is cathodically protected can be main-
tained in a corrosive environment without deterioration for an indefinite time.
There are two types of cathodic protection: impressed current cathodic protec-
tion (ICCP) and sacrificial anode cathodic protection (SACP), also known as
galvanic cathodic protection.
As discussed in Section 5.11, the mechanism of cathodic protection depends
on external current that polarizes the entire surface to the thermodynamic poten-
tial of the anode. The surface becomes equipotential (cathode and anode poten-
tials become equal), and corrosion currents no longer flow. Or, looked at another
way, at a high enough value of external current density, a net positive current
enters the metal at all regions of the metal surface (including anodic areas);
hence, there is no tendency for metal ions to enter into solution.
Cathodic protection can be applied in practice to protect metals, such as steel,
copper, lead, and brass, against corrosion in all soils and in almost all aqueous
media. Pitting corrosion can be prevented in passive metals, such as the stainless

251
252 C ATHODIC PROTEC TION
steels or aluminum. Cathodic protection can be used effectively to eliminate

stress-corrosion cracking (e.g., of brass, mild steel, stainless steels, magnesium,
aluminum), corrosion fatigue of most metals (but not fatigue), intergranular cor-
rosion (e.g., of Duralumin, 18–8 stainless steel), or dezincification of brass. It can
be used to avoid S.C.C. of high-strength steels, but not hydrogen cracking of such
steels. Corrosion above the water line (e.g., of water tanks) is not affected,
because the impressed current cannot reach metal areas that are out of contact
with the electrolyte. Nor does the protective current extend into electrically
screened areas, such as the interior of water condenser tubes (unless the auxiliary
anode enters the tubes), even though the water box may be adequately
protected.
13.2 BRIEF HISTORY
As a result of laboratory experiments in salt water, Sir Humphry Davy [1]

reported in 1824 that copper could be successfully protected against corrosion
by coupling it to iron or zinc. He recommended cathodic protection of copper-
sheathed ships, employing sacrificial blocks of iron attached to the hull in the
ratio of iron to copper surface of about 1 : 100. In practice, the corrosion rate of
copper sheathing was appreciably reduced, as Davy had predicted; but, unfortu-
nately, cathodically protected copper is subject to fouling by marine organisms,
contrary to the behavior of unprotected copper, which supplies a sufficient con-
centration of copper ions to poison fouling organisms (see Section 6.8.1). Because
fouling reduced the speed of ships under sail, the British Admiralty decided
against the idea. After Davy’s death in 1829, his cousin, Edmund Davy (Professor
of Chemistry at the Royal Dublin University), successfully protected the iron
work of buoys by attaching zinc blocks, and Robert Mallet, in 1840, produced a
zinc alloy particularly suited as a sacrificial anode. When wooden hulls were
replaced by steel, the fitting of zinc slabs became traditional on all Admiralty
vessels.* These slabs provided localized protection, especially against the galvanic
effects of the bronze propeller, but the overall cathodic protection of seagoing
ships was not explored again until about 1950, this time by the Canadian Navy
[2]. By using antifouling paints in combination with anticorrosion paints, it was
shown that cathodic protection of ships is feasible and can make possible appre-
ciable savings in maintenance costs. A cathodically protected, hence smooth, hull
also reduces fuel costs of ship operation.
Cathodic protection was incidental to the mechanism of protecting steel
sheet coated by dipping into molten zinc (galvanizing)(see Section 14.3.3), a
method first patented in France in 1836 and in England in 1837 [3]. However, the
practice of zinc coating of steel was apparently described in France as early as
1742 [4]. The first application of impressed electric current for protection of
underground structures took place in England and in the United States, about
*Communication of Dr. W. H. J. Vernon and Mr. L. Kenworthy with H.H.U.

HOW APPLIED 253
1910–1912 [3]. Since then, the general use of cathodic protection has spread
rapidly, and now tens of thousands of miles of buried pipeline and cables are
effectively protected against corrosion by this means. In many parts of the world,
cathodic protection of high-pressure oil and gas pipelines is a government-man-
dated regulatory requirement. Cathodic protection is also applied to canal gates,
condensers, submarines, water tanks, marine piling, offshore oil-drilling struc-
tures, chemical equipment, bridge decks, parking garages, and other reinforced
concrete structures (see Section 7.4).
13.3 HOW APPLIED
Cathodic protection requires a source of direct current and an auxiliary electrode

(anode) usually of iron or graphite located some distance away from the pro-
tected structure. The direct current (dc) source is connected with its positive ter-
minal to the auxiliary electrode and its negative terminal to the structure to be
protected; in this way, current flows from the electrode through the electrolyte
to the structure. The applied voltage is not critical—it need only be sufficient to
supply an adequate current density to all parts of the protected structure. In soils
or waters of high resistivity, the applied voltage must be higher than in environ-
ments of low resistivity. Or, when the extremities of a long pipeline are to be
protected by a single anode, the applied voltage must be raised. A sketch of a
cathodically protected buried pipeline is shown in Fig. 13.1.
Figure 13.1. Sketch of cathodically protected pipe, auxiliary anode, and rectifier.
The source of current is usually a rectifier supplying low-voltage dc of several

amperes. Motor generators have been used, although maintenance is trouble-
some. Windmill generators are employed in areas where prevailing winds are
dependable. Even in periods of calm, some degree of protection of steel persists
temporarily because of the inhibiting effect of alkaline electrolysis products at
the cathode surface.
13.3.1 Sacrificial Anodes

If the auxiliary anode is composed of a metal more active in the Galvanic Series
than the metal to be protected, a galvanic cell is set up with current direction
exactly as described in the previous section. The impressed source of current (i.e.,
the rectifier) can then be omitted, and the electrode is called a sacrificial anode,
as shown in Fig. 13.2. Sacrificial metals used for cathodic protection consist of
magnesium-base and aluminum-base alloys and, to a lesser extent, zinc. Sacrificial
anodes serve essentially as sources of portable electrical energy. They are useful
particularly when electric power is not readily available, or in situations where it
is not convenient or economical to install power lines for the purpose. The open-
circuit potential difference of magnesium with respect to steel is about 1 V (φH
for magnesium in seawater = −1.3 V), so that only a limited length of pipeline can
be protected by one anode, particularly in high-resistivity soils. This low voltage
is sometimes an advantage over higher impressed voltages in that danger of
overprotection to some portions of the system is less; and since the total current
per anode is limited, the danger of stray-current damage (interference problems)
to adjoining metal structures is reduced.
Figure 13.2. Cathodically protected pipe with sacrificial anode.

COMBINED USE WITH COATINGS 255
The potential of zinc is less than that of magnesium (φH in seawater = −0.8 V);
hence, current output per anode is also less. High-purity zinc is usually specified
in order to avoid significant anodic polarization with resultant reduction of
current output caused by accumulation of adherent insulating zinc reaction
products on commercial zinc. This tendency is less pronounced in zinc of high
purity.
Aluminum operates theoretically at a voltage between magnesium and zinc.
A disadvantage of aluminum as a sacrificial anode is that it tends to become
passive in water or in soils with accompanying shift of potential to a value
approaching that of steel. A special chemical environment high in chlorides sur-
rounding the electrode can be provided in order to avoid passivity; however, such
an environment, called backfill, is only a temporary measure. In seawater, passiv-
ity can be avoided by alloying additions, such as tin, indium, antimony, or mercury.
For example, alloying aluminum with 0.1% Sn followed by heat treatment at
620 °C for 16 h and water quenching to retain the tin in solid solution very much
decreases anodic polarization in chloride solutions [5]. The corrosion potential
of the 0.1% Sn alloy in 0.1N NaCl is −1.2 V (S.H.E.) compared to −0.5 V for pure
aluminum. Some sacrificial aluminum anodes contain about 0.1% Sn and 5% Zn
[6, 7]. Another composition containing 0.6% Zn, 0.04% Hg, and 0.06% Fe, when
tested in seawater for 254 days, operated at a current efficiency of 94% (1270 A-
h/lb); however, use of mercury has been banned in most locations because of
pollution concerns [8]. For cathodic protection of offshore platforms, aluminum
anodes, made from aluminum-zinc alloys, are the preferred material [8].
For offshore applications, magnesium anodes have not been popular since
the 1980s, because of improvements in aluminum and zinc anodes [8]. Magnesium
anodes may be consumed before the structure has reached the end of its lifetime,
whereas aluminum anodes are characterized by reliable long-term performance
[8]. Magnesium anodes are often alloyed with 6% Al and 3% Zn to reduce
pitting-type attack and to increase current efficiency. By using high-purity mag-
nesium containing about 1% Mn, the advantage of a higher potential (with higher
current output per anode) is obtained [9]. This alloy operates at a current effi-
ciency in seawater similar to the first-mentioned alloy, but at somewhat lower
efficiency in most soils. The observed efficiency of magnesium anodes averages
about 500 A-h/lb compared to a theoretical efficiency of 1000 A-h/lb.
A sketch of a magnesium anode rod installed in a steel hot-water tank is shown
in Fig. 13.3. Such rods may increase the life of a steel tank by several years, particu-
larly if the rod is renewed as required. The degree of protection is greater in waters
of high conductivity, where the currents naturally set up by the magnesium–iron
couple reach higher values than in waters of low conductivity (soft waters).
13.4 COMBINED USE WITH COATINGS
The distribution of current in a cathodically protected steel water tank is not

ideal—too much current may flow to the sides and not enough to the top and
Figure 13.3. Cathodically protected hot-water tank with magnesium anode.
bottom. Better distribution is accomplished by using an insulating coating (e.g.,

an organic coating at ordinary temperatures or a glass coating at elevated tem-
peratures). The insulating coating need not be pore-free, since the protective
current flows preferably to exposed metal areas, wherever located, which are
precisely the areas needing protection. Also, since the total required current is
less than that for an uncoated tank, the magnesium anode lasts longer.
In hard waters, a partially protective coating may form on steel that consists
largely of CaCO3 precipitated by alkalies generated as reaction products at the
cathode surface. A similar coating forms gradually on cathodically protected
surfaces exposed to seawater (more rapidly at high current densities). Such coat-
ings, if adherent, are also useful in distributing the protective current and in
reducing total current requirements.
In the general application of cathodic protection using either impressed
current or sacrificial anodes, it is expedient to use an insulating coating, and this
MAGNITUDE OF CURRENT REQUIRED 257
combination is the accepted practice today. For example, the distribution of

current to a coated pipeline is much improved over that to a bare pipeline; the
total current and required number of anodes are less; and the total length of
pipeline protected by one anode is much greater. Since the earth, taken as a
whole, is a good electrical conductor, and the resistivity of the soil is localized
only within the region of the pipeline or the electrodes, one magnesium anode
can protect as much as 8 km (5 miles) of a coated pipeline. For a bare pipeline,
the corresponding distance might be only 30 m (100 ft). Using an impressed
current at higher applied voltages, one anode might protect as much as 80 km
(50 miles) of a coated pipeline. The limiting length of pipe protected per anode
is imposed not by resistance of the soil, but by the metallic resistance of the
pipeline itself.
The potential decay, Ex, along an infinite pipeline measured from the point
of attachment to the dc source having potential EA is expressed as an exponential
relation with respect to distance, x, along the pipeline in accord with
(
⎡ 2 πrRL
)
12
⎤
Ex = EA exp ⎢ − x⎥ (13.1)
⎣ kz ⎦
Both Ex and EA represent differences between polarized potential with current

flowing and corrosion potential in absence of current, RL is the resistance of pipe
of radius r per unit length, k is a constant, and z is the resistance of pipe coating
per unit area (for derivation, see Appendix, Section 29.4). This equation is derived
by assuming that polarization of the cathodically protected surface is a linear
function of current density. Note that Ex becomes zero at x = ∞.
Considering a finite pipeline for which a/2 is half the distance to the next
point of bonding, and potential Ex at a/2 = EB,
(
⎡ 2 πrRL
) (x − a2 )⎤⎥⎦
12
Ex = EB cosh ⎢ (13.2)
⎣ kz
Cathodic protection is optimum within a specific potential range (see Section

13.7), so that the length of pipeline protected by one anode increases as the
metallic pipe resistance, RL, decreases, and coating resistance, z, increases.
13.5 MAGNITUDE OF CURRENT REQUIRED
The current density required for complete protection depends on the metal and
on the environment. It can be seen from Fig. 5.15 in Section 5.11 that the applied
current density must always exceed the current density equivalent to the mea-
sured corrosion rate in the same environment. Hence, the greater the corrosion
rate, the higher must be the impressed current density for protection.
When the corrosion rate is cathodically controlled and the corrosion poten-
tial approaches the open-circuit anode potential, the required current density is
TABLE 13.1. Orders of Magnitude of Current Density

Required for Cathodic Protection of Steel
Environment A/m2 A/ft2
Sulfuric acid pickle (hot) 400 35

Soils 0.01–0.5 0.001–0.05
冦
Moving seawater 0.03 (final) 0.003
0.15 (initial) 0.015
Air-saturated water (hot) 0.15 0.015
Moving fresh water 0.05 0.005
only slightly greater than the equivalent corrosion current. But for mixed control,
the required current can be considerably greater than the corrosion current, and
it is still greater for corrosion reactions that are anodically controlled.
If the protective current induces precipitation of an inorganic scale on the
cathode surface, such as in hard waters or in seawater, the total required current,
as described earlier, falls off as the scale builds up. However, at exposed areas of
metal, the current density remains the same as before scale formation; only the
total current density per apparent unit area is less.
The precise requirements of current density for complete protection can be
determined in several ways; the most important is potential measurement of the
protected structure (see Section 13.7). In the absence of such measurements, only
orders of magnitude can be given. These are listed in Table 13.1 for steel exposed
to various environments.
13.6 ANODE MATERIALS AND BACKFILL
Auxiliary anodes for use with impressed current are usually composed of scrap
iron or graphite. Scrap iron is consumed at the rate of 15–20 lb/A-year and must
be renewed periodically. Graphite anodes are consumed at a lower rate, not
exceeding perhaps 2 lb/A-year. Graphite costs more than scrap iron, both initially
and in subsequent higher electrical power costs because of the noble potential
and accompanying high overpotential of oxygen (or Cl2) evolution on graphite
compared to an active potential and lower overvoltage for the reaction Fe → Fe2+
+ 2e−. Graphite is also fragile compared to scrap iron and must be installed with
greater care. The advantages and disadvantages of graphite apply in similar
measure to 14% Si−Fe alloy anodes and magnetite anodes, which have also been
recommended.
For protection of structures in seawater, platinum-clad copper, 2% Ag−Pb,
platinized titanium, or platinized niobium have been recommended as corrosion-
resistant anodes using impressed current [10–12]. Whereas sacrificial magnesium
anodes require replacement approximately every 2 years, the 2% Ag−Pb anodes
are estimated to last more than 10 years, and the 90% Pt–10% Ir anodes still
ANODE MATERIALS AND BACKFILL 259
longer [11]. In fresh waters, aluminum anodes are sometimes used for impressed
current systems.
Because the effective resistivity of soil surrounding an anode is confined to
the immediate region of the electrode, it is common practice to reduce local
resistance by backfill. For impressed current systems, this consists of surrounding
the anode with a thick bed of coke and adding a mixture of perhaps 3 or 4 parts
gypsum (CaSO4·H2O) to 1 part NaCl. The coke backfill, being a conductor, carries
part of the current, reducing in some measure consumption of the anode itself.
Backfill may not be required if the anode is immersed in a river bed, lake, or the
ocean.
Whereas auxiliary anodes need not be consumed in order to fulfill their
purpose, sacrificial anodes are consumed not less than is required by Faraday’s
law in order to supply an equivalent electric current. In general, the observed
rate of consumption is greater than the theoretical. For zinc the difference is not
large, but for magnesium it is appreciable, with the cause being ascribed to local-
action currents on the metal surface, to formation of colloidal metal particles [13,
14] or, perhaps more important, to initial formation of univalent magnesium ions
[15]. The latter ions are unstable and react in part with water in accord with
2Mg + + 2 H 2O → Mg(OH)2 + Mg 2+ + H 2
Hence, in dilute sodium chloride, about half the magnesium corroding anodically
appears as Mg(OH)2 and half as MgCl2, accompanied by hydrogen evolution in
about the amount expected according to this reaction [15]. Additional lesser side
reactions may also take place at the same time. Accordingly, the observed yield
of a magnesium anode is only about one-half the 1000 A-h/lb calculated on the
basis of Mg2+ formation.
For magnesium anodes, backfill has the advantage of reducing resistance of
insulating corrosion-product films, such as Mg(OH)2, as well as increasing
conductivity of the immediate environment. A suitable backfill may consist of
approximately 20% bentonite (an inorganic colloid used for retention of mois-
ture), 75% gypsum, and 5% Na2SO4. Sometimes, the backfill is packaged before-
hand in a bag surrounding the anode, so that anode and backfill can be placed
simultaneously into position in the soil.
13.6.1 Overprotection
Moderate overprotection of steel structures usually does no harm. The main dis-
advantages are waste of electric power and increased consumption of auxiliary
anodes. In the extreme, additional disadvantages result if so much hydrogen is
generated at the protected structure that blistering or disbonding of organic coat-
ings, hydrogen embrittlement of the steel (loss of ductility through absorption of
hydrogen), or hydrogen cracking (see Section 8.4) is caused. Damage to steel by
hydrogen absorption is particularly apt to occur in environments containing sul-
fides [16] for reasons discussed in Section 5.5.
In the case of amphoteric metals, such as aluminum, zinc, lead, and tin, excess
alkalies generated at the surface of overprotected systems damage the metals by
causing increased attack rather than reduction of corrosion. It was shown that
cathodic protection of lead continues into the alkaline range of pH, but the criti-
cal potential for complete protection (see below) shifts to more active values [17].
Aluminum can be cathodically protected against pitting by coupling it to zinc
[18] used as a sacrificial anode; but if coupled to magnesium, overprotection may
result with consequent damage to the aluminum.
13.7 CRITERIA OF PROTECTION
The effectiveness of cathodic protection in practice can be established in more

than one way, and several criteria have been used in the past to prove whether
protection is complete. For example, the observed number of leaks in an old
buried pipeline is plotted against time, noting that leaks per year drop to a small
number or to zero after cathodic protection is installed. Or the hull of a ship can
be inspected at regular intervals for depth of pits.
It is also possible to check effectiveness of protection by short-time tests,
including the following measures:
1. Coupon Tests. A weighed metal coupon shaped to conform to the outside

surface of a buried pipe is attached by a brazed connecting cable, and both
the cable and surface between coupon and pipe are overlaid with coal tar.
After exposure to the soil for a period of weeks or months, the weight loss,
if any, of the cleaned coupon is a measure of whether cathodic protection
of the pipeline is complete.
2. Colorimetric Tests. A section of buried pipeline is cleaned, exposing bare
metal. A piece of absorbent paper soaked in potassium ferricyanide solu-
tion is brought into contact, and the soil is returned in place. After a rela-
tively short time, examination of the paper for the blue color of ferrous
ferricyanide indicates that cathodic protection is not complete, whereas
absence of blue indicates satisfactory protection.
Both the coupon and the colorimetric tests are qualitative and do not provide
information about whether just enough or more than enough current is being
supplied.
13.7.1 Potential Measurements

A criterion that indicates degree of protection, including overprotection, is
obtained through measuring the potential of the protected structure. This mea-
surement is of greatest importance in practice, and it is the criterion generally
accepted and used by corrosion engineers. It is based on the fundamental concept
that optimum cathodic protection is achieved when the protected structure is
CRITERIA OF PROTECTION 261
polarized to the open-circuit anode potential of local-action cells. This potential

for steel, as determined empirically, is equal to −0.85 V versus the copper-
saturated CuSO4 half-cell, or −0.53 V (S.H.E.).
The theoretical open-circuit anode potential for iron can be calculated assum-
ing that the activity of Fe2+ in equilibrium is determined by the solubility of a
covering layer of Fe(OH)2, in accord with previous discussions of oxide-film
composition on iron exposed to aqueous media (see Section 7.1). Using the
Nernst equation, we obtain
0.059 solubility product

φ H = −0.44 + log (Fe2+ ), where ( Fe2+ ) =
2 (OH −)2
The value of (OH−) can be estimated assuming that its concentration at equilib-
rium is twice that of (Fe2+), in accord with Fe(OH)2 → Fe2+ + 2(OH−).* The
potential so calculated is −0.59 V (S.H.E.), equivalent to a potential difference of
−0.91 V versus copper-saturated CuSO4, and is in essential agreement with the
empirical value.
The empirical value for lead, known only approximately [19], is about −0.78 V
versus copper-saturated CuSO4 compared to the calculated value for a Pb(OH)2
film on lead equal to −0.59 V. In alkaline media, with formation of plumbites, the
calculated value comes closer to the empirical value.† Other calculated values are
listed in Table 13.2.
For passive metals, the criterion of protection differs from that just described.
Since passive metals corrode uniformly at low rates, but by pitting corrosion at
high rates, cathodic protection of metals like aluminum and 18–8 stainless steel
depends on polarizing them not to the usual thermodynamic anode potential, but
only to a value more active than the critical potential at which pitting initiates
(see Section 6.6). The latter potential lies within the passive range and is less
noble the higher the Cl− concentration; in 3% NaCl the value for aluminum is
−0.45 V (S.H.E.). Hence, iron with a corrosion potential in seawater of about
−0.4 V is not suited as a sacrificial anode for cathodically protecting aluminum,
unlike zinc, which has a more favorable corrosion potential of about −0.8 V. For
18–8 stainless steel, the critical potential in 3% NaCl is 0.21 V; for nickel it is about
0.23 V. Coupling of the latter metals to a suitable area of either iron or zinc,
therefore, can effectively protect them cathodically in seawater against initiation
*This relation holds for a saturated solution of Fe(OH)2 in water, the natural pH of which is 9.5. This
pH is observed at an iron surface between an external pH of 4–10, as discussed in Section 7.2.3. Values
of surface pH for other corroding metals are specific to the metal; but the relation (2M2+) = (OH−)
also applies, provided that the external solution in contact does not alter the natural pH of the surface
metal hydroxide.
†
A similar situation applies to Cd assumed to be coated with a film of Cd(OH)2 (solubility product
= 2 × 10−14). The calculated value of φH is −0.54, which is noble to iron, contrary to an observed galvanic
potential less noble than iron (see Fig. 3.3, Section 3.8). The observed more-active galvanic potential
of cadmium is plausibly explained by the known tendency of Cd2+ to form complex ions that lower
Cd2+ activity below the value corresponding to saturated Cd(OH)2.
TABLE 13.2. Calculated Minimum Potential φ for Cathodic Protection

Metal φ° (volts) Solubility Product, φH (volts) φH versus Cu−CuSO4
M(OH)2 Reference Electrode
(volts)
Iron −0.440 1.8 × 10−15 −0.59 −0.91

Copper 0.337 1.6 × 10−19 0.16 −0.16
Zinc −0.763 4.5 × 10−17 −0.93 −1.25
Lead −0.126 4.2 × 10−15 −0.27 −0.59
of pitting corrosion. Components of practical structures, such as ships and off-

shore oil-drilling platforms, are sometimes designed to take advantage of galvanic
couples of this kind.
13.7.2 Doubtful Criteria

Criteria have sometimes been suggested based on empirical rules—for example,
polarizing a steel structure 0.3 V more active than the corrosion potential. This
criterion is not exact and in many situations leads to under- or overprotection. It
has also been suggested that polarization of the structure should proceed to
breaks in slope of the voltage versus current plot. Such breaks may, in principle,
occur in some environments when the applied current is just equal to or slightly
greater than the corrosion current (e.g., oxygen depolarization control); but in
other environments, breaks may occur when concentration polarization or IR
effects through partially protective surface films become appreciable. As Stern
and Geary showed [20], breaks of this kind in polarization measurements have
varied causes and are of doubtful value as criteria of cathodic protection. Con-
trary to what is sometimes erroneously supposed, discontinuities in slopes of
polarization curves have no general relation to the anode or cathode open-circuit
potentials of the corroding system.
13.7.3 Position of Reference Electrode

The potential of a cathodically protected structure is determined ideally by
placing the reference electrode as close as possible to the structure to avoid an
error caused by IR drop through the electrolyte. Any IR drop through corrosion-
product films or insulating coatings will persist, of course, even where adequate
precautions are exercised otherwise, tending to make the measured potential
more active than the actual potential at the metal surface. In practice, for buried
pipelines, a compromise position is chosen at the soil surface located directly over
the buried pipe. This position is chosen because cathodic protection currents flow
mostly to the lower surface and are minimal to the upper surface of a pipe buried
a few feet below the soil surface.
ANODIC PROTECTION 263
The reference electrode is sometimes located at a position remote from the

pipeline, recommended because currents do not penetrate remote areas, and
hence, IR drop effects are avoided. Actually, the potential measured at a remote
position is a compromise potential at some value between that of the polarized
structure and the polarized auxiliary or sacrificial anode. These potentials differ
by the IR drop through the soil and through coatings. The potential measured at
a remote location, therefore, tends to be more active than the true potential of
the structure, resulting in a structure that may be underprotected.
13.8 ECONOMICS OF CATHODIC PROTECTION
For buried pipelines, the cost of cathodic protection is far less than for any other
means offering equal assurance of protection. The guarantee that no leaks will
develop on the soil side of a cathodically protected buried pipeline makes it
economically feasible, for example, to transport oil and high-pressure natural gas
across entire continents.
In addition, lack of corrosion on the soil side makes it possible to specify
thinner wall pipe adequate to withstand internal pressures and to avoid any extra
thickness as a safety factor against corrosion. This saving alone is substantial. The
Panama Canal gates, for example, are protected by using impressed current, with
the initial costs of installation being less than 0.5% the cost of replacing the gates.
One important advantage is that the gates can continue to operate without the
necessity of periodic long shutdowns for repairs caused by corrosion. Similarly,
a ship that is cathodically protected can operate, in principle, for longer periods
between dry-docking, thereby saving thousands of dollars annually. The further
economic advantages, in other instances, through avoiding stress-corrosion crack-
ing, corrosion fatigue, and pitting of various structural metals are substantial in
terms of extended lifetime, enhanced reliability, and assured public safety.
13.9 ANODIC PROTECTION
As mentioned in Section 6.4, some metals, such as iron and stainless steels, can
also be protected by making them anodic and shifting their potential into the
passive region of the anodic polarization curve (see Fig. 6.1, Section 6.2). The
passive potential is automatically maintained, usually electronically, by an instru-
ment called the potentiostat. Practical application of anodic protection and use
of the potentiostat for this purpose were first suggested by Edeleanu [21].
Anodic protection has found application in handling sulfuric acid [22], but
the method is also applicable to other acids (e.g., phosphoric acid) and to alkalies
and some salt solutions. It has been shown to be effective for increasing the
resistance to corrosion fatigue of various stainless steels in 0.5M Na2SO4 [23], in
10% H2SO4 or 10% NH4NO3, and of 0.19% C steel in 10% NH4NO3 [24].
Engineering installations have been described for anodically protecting mild
steel against uniform corrosion in NH4NO3 fertilizer mixtures [25], carbon steel
in 86% spent sulfuric acid at temperatures up to 60 °C (140 °F) [26], and carbon
steel in 0.1–0.7M oxalic acid at temperatures up to 50 °C (120 °F) [27].
Since passivity of iron and the stainless steels is destroyed by halide ions,
anodic protection of these metals is not possible in hydrochloric acid or in acid
chloride solutions for which the current density in the otherwise passive region
is very high. Also, if Cl− should contaminate the electrolyte, the possible danger
of pitting becomes a consideration even if the passive current density remains
acceptably low. In the latter case, however, it is only necessary to operate in the
potential range below the critical pitting potential for the mixed electrolyte.*
Titanium, which has a very noble critical pitting potential over a wide range of
Cl− concentration and temperature, is passive in the presence of Cl− (low ipassive)
and can be anodically protected without danger of pitting even in solutions of
hydrochloric acid.
Anodic protection is applicable only to metals and alloys (mostly transition
metals) which are readily passivated when anodically polarized and for which
ipassive is very low. It is not applicable, for example, to zinc, magnesium, cadmium,
silver, copper, or copper-base alloys. Anodic protection of aluminum exposed to
high-temperature water has been shown to be feasible (see Section 21.1.2).
Current densities to initiate passivity, icritical, are relatively high, with 6 A/m2
being required for Type 316 stainless steel in 67% H2SO4 at 24 °C (75 °F). But
currents for maintaining passivity are usually low, with the orders of magnitude
being 10−3 A/m2 (0.1 μA/cm2) for Type 316 stainless steel to 0.15 A/m2 (15 μA/cm2)
for mild steel [22], both in 67% H2SO4. Corrosion rates corresponding to these
current densities are 0.02–2.5 gmd.
It is typical of anodic protection that corrosion rates, although small, are not
reduced to zero, contrary to the situation for cathodic protection of steel. On the
other hand, the required current densities in corrosive acids are usually much
lower than those for cathodic protection, since for cathodic protection the current
cannot be less than the normal equivalent corrosion current in the same environ-
ment. For stainless steels, this value of current density corresponds to the rather
high corrosion rate for the active state of the alloys.
For anodic protection, it has been reported [22] that unusual throwing power
(protection at distances remote from the cathode or in electrically screened
areas) is obtained, far exceeding similar throwing power obtained in cathodic
protection. The cause has been ascribed to high electrical resistance of the passive
film, but this is probably not correct, because measurements have shown that
such resistances are typically low. The cause instead may be related to the
corrosion-inhibiting properties of anodic corrosion products released by stainless
steels in small amounts (e.g., S2O82−, Cr2O72− , Fe3+), which shift the corrosion poten-
tial into the passive region in the absence of an applied current.
*Stress-corrosion cracking of Type 304 stainless steel, which is reported to occur at room temperature
in 10N H2SO4 + 0.5N NaCl, is prevented by anodically polarizing the alloy to 0.7 V (S.H.E.). See
S. Acello and N. Greene, Corrosion 18, 286t (1962); J. Harston and J. Scully, Corrosion 25, 493 (1969).
REFERENCES
1. H. Davy, Philos. Trans. Roy. Soc. 114, 151–158, 242–246, 328–346 (1824–1825).
2. K. Barnard (with G. Christie), Corrosion 6, 232 (1950); ibid. 7, 114 (1951); (with G.
Christie and J. Greenblatt), ibid. 9, 246 (1953).
3. W. Lynes, J. Electrochem. Soc. 98, 3c (1951).
4. R. Burns and W. Bradley, Protective Coatings for Metals, 3rd edition, Reinhold, New
York, 1967, pp. 104–106.
5. D. Keir, M. Pryor, and P. Sperry, J. Electrochem. Soc. 114, 777 (1967); ibid. 116, 319
(1969).
6. J. Burgbacher, Mater. Prot. 7, 26 (1968).
7. T. Lennox, M. Peterson, and R. Groover, Mater. Prot. 7, 33 (1968).
8. R. H. Heidersbach, J. Brandt, D. Johnson, and J. S. Smart III, Marine corrosion protection,
in ASM Handbook, Vol. 13C, Corrosion: Environments and Industries, ASM Interna-
tional, Materials Park, OH, 2006, p. 73.
9. P. George, J. Newport, and J. Nichols, Corrosion 12, 627t (1956).
10. H. Preiser and B. Tytell, Corrosion 15, 596t (1959).
11. K. Barnard, G. Christie, and D. Gage, Corrosion 15, 581t (1959).
12. R. Benedict, Mater. Prot. 4, 36 (Dec. 1965).
13. G. Marsh and E. Schashl, J. Electrochem. Soc. 107, 960 (1960).
14. G. Hoey and M. Cohen, J. Electrochem. Soc. 105, 245 (1958).
15. J. Greenblatt, J. Electrochem. Soc. 103, 539 (1956); (with E. Zinck) Corrosion 15, 76t
(1959); ibid. 18, 125t (1962).
16. W. Bruckner and K. Myles, Corrosion 15, 591t (1959).
17. W. Bruckner and O. Jansson, Corrosion 15, 389t (1959).
18. R. Mears and H. Fahrney, Trans. Am Inst. Chem. Eng. 37, 911 (1941).
19. D. Werner, Corrosion 13, 68 (1957).
20. M. Stern and A. Geary, J. Electrochem. Soc. 104, 56 (1957).
21. C. Edeleanu, Nature 173, 739 (1954); Metallurgia 50, 113 (1954).
22. O. Riggs, M. Hutchison, and N. Conger, Corrosion 16, 58t (1960).
23. H. Spähn, Z. Phys. Chem. (Leipzig) 234, 1 (1967).
24. W. Cowley, F. Robinson, and J. Kerrich, Br. Corros. J. 3, 223 (1968).
25. W. Banks and M. Hutchison, Mater. Prot. 8, 31 (February 1969).
26. L. Hays, Mater. Prot. 5, 46 (1966).
27. L. Perrigo, Mater. Prot. 5, 73 (1966).
GENERAL REFERENCES
C. A. Brebbia, V. G. DeGiorgi, and R. A. Adey, editors, Cathodic protection systems, Section

1 in Simulation of Electrochemical Processes, WIT Press, Southampton, U.K., 2005,
pp. 1–56.
J. H. Fitzgerald III, Engineering of cathodic protection systems, in Uhlig’s Corrosion
Handbook, 2nd edition, Wiley, New York, 2000, pp. 1061–1078.
R. H. Heidersbach, Cathodic protection, in ASM Handbook, Vol. 13A, Corrosion: Funda-

mentals, Testing, and Protection, ASM International, Materials Park, OH, 2003,
pp. 855–870.
R. H. Heidersbach, J. Brandt, D. Johnson, and J. S. Smart III, Marine corrosion protection, in
ASM Handbook, Vol. 13C, Corrosion: Environments and Industries, ASM Interna-
tional, Materials Park, OH, 2006, pp. 73–78.
C. E. Locke, Anodic protection, in ASM Handbook, Vol. 13A, Corrosion: Fundamentals,
Peabody’s Control of Pipeline Corrosion, 2nd edition, R. L. Bianchetti, editor, NACE
International, Houston, TX, 2001.
O. Riggs, Jr. and C. Locke, Anodic Protection, Theory and Practice in the Prevention of
Corrosion, Plenum Press, New York, 1981.
PROBLEMS
1. Sketch the polarization diagram of a buried steel pipe connected to a sacri-

ficial magnesium anode. Indicate the following on the diagram:
(a) The potential near the pipe surface with respect to the open-circuit
potentials of anodic and cathodic areas of the pipe.
(b) The potential of the pipe with the reference electrode located far from
and at right angles to the pipe.
(c) The change in potential of the pipe proceeding toward the vicinity of the
magnesium anode.
2. Calculate the minimum potential versus Cu−CuSO4 reference electrode
to which zinc must be polarized for complete cathodic protection, assuming
Zn(OH)2 as corrosion product on the surface. (Solubility product of
Zn(OH)2 = 4.5 × 10−17.)
3. From sketches of polarization diagrams of a corroding metal, compare applied

current, as required for complete cathodic protection, to the normal corro-
sion current when:
(a) The corrosion rate is anodically controlled.
(b) The corrosion rate is cathodically controlled.
4. Current between a magnesium anode and a 50-gal steel tank filled with air-
saturated hot water is 100 mA. Disregarding local-action currents, what inter-
val of time is required between filling and emptying the tank to ensure
minimum corrosion of outlet steel water piping? (Solubility of oxygen in inlet
water, 25 °C, = 6 mL/liter.)
5. Iron corrodes in seawater at a rate of 2.5 gmd. Assuming that all corrosion
is by oxygen depolarization, calculate the minimum initial current density
(A/m2) necessary for complete cathodic protection.
PROBLEMS 267
6. Calculate the minimum potential versus saturated calomel electrode to which

copper must be polarized in 0.1M CuSO4 for complete cathodic protection.
7. A copper bar of 300-cm2 total exposed area coupled to an iron bar 50-cm2
area is immersed in seawater. What minimum current must be applied to the
couple in order to avoid corrosion of both iron and copper? (Corrosion rate
of uncoupled iron in seawater is 0.13 mm/y.)
8. To what minimum potential versus saturated calomel electrode must indium

be polarized in 0.01M In2(SO4)3 solution for complete cathodic protection?
[Data: In3+ + 3e− → In, φo = −0.342 V; γ0.01M In2(SO4)3 = 0.142.]
9. (a) How many milliliters H2 (S.T.P.) are evolved per square centimeter per
day from a steel surface maintained at the critical potential for cathodic
protection, φH = −0.59 V?
(b) Similarly, how many milliliters H2 are evolved if cathodic protection is
increased to a potential 0.1 V more active than the critical value? [Data:
Assume hydrogen overpotential (volts) on steel = 0.105 log i/(1 × 10−7),
where i = A/cm2, pH of steel surface = 9.5.]
10. You have been asked to review a proposal to cathodically protect a structure
in an aqueous environment with a pH of approximately 7. The structure will
be constructed of a high-strength steel that is very susceptible to hydrogen
cracking. Discuss the factors to be considered in deciding on how to protect
the structure from corrosion without causing failure by hydrogen cracking.
11. Under what circumstances can cathodic protection (either sacrificial protec-
tion or impressed current protection) be used to protect an automobile from
corrosion?
Answers to Problems
2. −1.25 V
4. 49.9 h.
5. 0.10 A/m2.
6. 0.042 V.
7. 3.8 × 10−3 A.
8. −0.634 V.
9. (a) 0.0019 mL/cm2-day; (b) 0.018 mL/cm2-day.
14
METALLIC COATINGS
14.1 METHODS OF APPLICATION
Metal coatings are applied by dipping, electroplating, spraying, cementation, and

diffusion. The selection of a coating process for a specific application depends on
several factors, including the corrosion resistance that is required, the anticipated
lifetime of the coated material, the number of parts being produced, the produc-
tion rate that is required, and environmental considerations.
Hot dipping is carried out by immersing the metal on which the coating is to
be applied, usually steel, in a bath of the molten metal that is to constitute the
coating, most commonly zinc, but also aluminum and aluminum–zinc alloys. Hot
dipping can be either a continuous process, as in galvanizing steel sheet,
or a batch process—for example, galvanizing fabricated parts, nuts, bolts, and
fasteners [1].
In electroplating, the substrate, or base, metal is made the cathode in an
aqueous electrolyte from which the coating is deposited. Although the primary
purpose of electroplating coatings is to achieve corrosion resistance, these coat-
ings can also be decorative, with a metallic luster after polishing [2]. A wide of
variety of coatings can be applied by electroplating—for example, zinc, cadmium,
chromium, copper, gold, nickel, tin, and silver, as well as alloys, such as tin–zinc,

269
270 METALLIC COATINGS
zinc–nickel, brass, bronze, gold alloys, and nickel alloys [2]. Electrogalvanizing is
the electroplating of zinc on either iron or steel. Electroplated zinc-coated sheet
is widely used for exposed automobile body panels because of its uniform coating
thickness and surface characteristics compared to hot-dip zinc-coated. Coatings
range in thickness from 4 to 14 μm [3].
Coatings are also produced by electroless plating—that is, by chemical reduc-
tion of metal–salt solutions, with the precipitated metal forming an adherent
overlay on the base metal. Nickel coatings of this kind are called electroless nickel
plate.
In thermal spraying of metal coatings, a gun is used that simultaneously melts
and propels small droplets of metal onto the surface to be coated. There are several
types of thermal spraying, with the three main variables in each type being the
temperature of the flame, the velocity of the particles that are sprayed onto
the substrate to form the coating, and the nature of the material that is to form the
coating (i.e., powder, rod, wire, or liquid) [4, 5]. The material that is to form the
coating is called the “feedstock.” In all cases, the feedstock is rapidly heated and
propelled toward the substrate where, on impact, it consolidates forming an adher-
ent coating. In flame-powder spraying, powder feedstock is melted and carried by
the flame onto the workpiece. In flame-wire spraying, the flame melts the wire, and
a stream of air propels the molten material onto the workpiece. In plasma spraying,
a plasma at a temperature of about 12,000 °C is formed, and the plasma stream
carries the powder feedstock to the workpiece [4].
Thermally sprayed coatings tend to be porous, although porosity can be
controlled by optimizing the process variables [4]. These coatings can be made
adherent and of almost any desired thickness, and they can be applied on already
fabricated structures. Sometimes, pores are filled with a thermoplastic resin in
order to increase corrosion protection.
Cementation consists of tumbling the work in a mixture of metal powder and
a flux at elevated temperatures, allowing the metal to diffuse into the base metal.
Aluminum and zinc coatings can be prepared in this way. Diffusion coatings of
chromium, nickel, titanium, aluminum, and so on, can also be prepared by immers-
ing metal parts, under an inert atmosphere, in a bath of molten calcium containing
some of the coating metal in solution [6].
Coatings are also sometimes produced by gas-phase reaction. For example,
CrCl2, when volatilized and passed over steel at about 1000 °C (1800 °F), results
in formation of a chromium–iron alloy surface containing up to 30% Cr in accord
with the reaction
3 3
CrCl 2 + Fe → FeCl 3 + Cr (alloyed with Fe)
2 2
Similar surface alloys of silicon–iron containing up to 19% Si can be prepared

by reaction of iron with SiCl4 at 800–900 °C (1475–1650 °F).
Ion implantation is a process of producing thin surface alloy coatings by
bombarding the metal with ions in vacuum. Such coatings of, for example, Ti, B,
CL ASSIFICATION OF COATINGS 271
Cr, or Y have specialized applications for wear and high-temperature oxidation

resistance [7, 8].
14.2 CLASSIFICATION OF COATINGS
All coatings provide barrier protection; that is, they provide a barrier between
the corrosive environment and the metal substrate; however, all commercially
prepared metal coatings are porous to some degree. Furthermore, coatings tend
to become damaged during shipment or in use. Therefore, galvanic action at the
base of a pore or scratch becomes an important factor in determining coating
performance. From the corrosion standpoint, metal coatings can be divided into
two classes, namely, noble coatings, which provide only barrier protection, and
sacrificial coatings, which, in addition to barrier protection, also provide cathodic
protection.
As the names imply, noble coatings (e.g., nickel, silver, copper, lead, or chro-
mium) on steel are noble in the Galvanic Series with respect to the base metal.
At exposed pores, the direction of galvanic current accelerates attack of the base
metal and eventually undermines the coating (Figs. 14.1 and 14.2); consequently,
it is important that noble coatings always be prepared with a minimum number
of pores and that any existing pores be as small as possible, to delay access of
water to the underlying metal. This usually means increasing the thickness of
coating. Sometimes, the pores are filled with an organic lacquer, or a second
metal, of lower melting point, is diffused into the coating at elevated tempera-
tures (e.g., zinc or tin into nickel).
For sacrificial coatings (e.g., zinc, cadmium) and, in certain environments, also
aluminum and tin on steel, the direction of galvanic current through the electro-
lyte is from coating to base metal; as a result, the base metal is cathodically pro-
tected (Fig. 14.1). As long as adequate current flows and the coating remains in
electrical contact, corrosion of the base metal does not occur. The degree of
Figure 14.1. Sketch of current flow at defects in noble and sacrificial coatings.
Figure 14.2. Undermining of nickel electrodeposit on steel by galvanic corrosion in 3% NaCl

solution (100×). Crack resulted from cyclic stressing in a corrosion-fatigue test [H. Spähn and
K. Fässler, Werkst Korros. 17, 321 (1966)].
porosity of sacrificial coatings, therefore, is not of great importance, contrary to

the situation for noble coatings. In general, of course, the thicker the coating, the
longer cathodic protection continues.
The area of base metal over which cathodic protection extends depends on
the conductivity of the environment. For zinc coatings on steel in waters of low
conductivity, such as distilled or soft waters, a coating defect about 3 mm (1/8 in.)
wide may begin to show rust at the center. However, in seawater, which is a good
conductor, zinc protects steel several decimeters or feet removed from the zinc.
This difference in behavior results from adequate current densities for cathodic
protection extending over a considerable distance in waters of high conductivity,
whereas cathodic current densities in waters of low conductivity fall off rapidly
with distance from the anode.
14.3 SPECIFIC METAL COATINGS
14.3.1 Nickel Coatings

Nickel coatings are usually prepared by electroplating. The metal is plated either
directly on steel or sometimes over an intermediate coating of copper. The copper
underlayer is used to facilitate buffing of the surface on which nickel is plated,
because copper is softer than steel, and also to reduce the required thickness of
nickel (which costs more than copper) for obtaining a coating of minimum poros-
ity. The automotive industry uses nickel as an underlayer for microcracked chro-
mium to protect steel [9].
SPECIFIC METAL COATINGS 273
Because porosity is an important factor in the life and appearance of nickel

coatings, a certain minimum thickness is recommended, depending on exposure
conditions. For indoor exposures, a coating 0.008–0.013 mm (0.3–0.5 mil) is con-
sidered adequate for many applications. For outdoor exposures, a coating 0.02–
0.04 mm (0.8–1.5 mil) may be specified. The thicker coatings in this range (or still
thicker) are desirable (e.g., for auto bumpers) for use near the sea coast or in
industrial environments, but thinner coatings are usually adequate for dry or
unpolluted atmospheres. For use in the chemical industry, nickel coatings com-
monly range from 0.025–0.25 mm (1–10 mils) thick.
Nickel is sensitive to attack, particularly by industrial atmospheres. In the
phenomenon called fogging, coatings tend to lose their specular reflectivity
because a film of basic nickel sulfate forms that decreases surface brightness [10].
To minimize fogging, a very thin (0.0003–0.0008 mm; 0.01–0.03 mil) coating of
chromium is electrodeposited over the nickel. This thin chromium overlayer has
led to the term “chrome plate,” although, in reality, such coatings are composed
mostly of nickel.
Optimum protection is obtained with “microcracked” chromium, electrode-
posited with many inherent microscopic cracks. The many cracks in chromium
favor initiation of corrosion at numerous sites, thereby decreasing depth of pen-
etration that would otherwise result from attack at fewer sites. The density of
cracks in chromium deposits varies from 0 to more than 120 cracks/mm, depend-
ing on bath chemistry, current density, and temperature [11]. The chromium
deposit usually overlies a thin nickel coating formed from a plating bath contain-
ing additives (usually sulfur compounds) that improve surface brightness (bright
nickel). This thin coating, in turn, overlies a matte coating two to three times
thicker, electrodeposited from a conventional nickel plating bath. The bright
nickel, which includes a small amount of sulfur, is anodic to the underlying nickel
coating of lower sulfur content, so that the bright nickel acts as a sacrificial
coating. Any pit beginning under the chromium coating tends to grow sidewise
rather than through the nickel layers. In this way, appearance of rust is delayed
and the multiple coating system is more protective for a given thickness of chro-
mium and nickel [12].
Electroless nickel plate is produced primarily for the chemical industry.
Nickel salts are reduced to the metal by sodium hypophosphite solutions at or
near the boiling point. A typical solution is the following:
NiCl2·6H2O 30 g/liter
Sodium hypophosphite 10 g/liter
Sodium hydroxyacetate 50 g/liter
pH 4–6
This particular formulation deposits nickel at the rate of about 0.015 mm

(0.6 mil)/h in the form of a nickel–phosphorus alloy [13]. The usual range of
phosphorus content in coatings of this kind is 7–9%. Various metal surfaces,
including nickel, act as catalysts for the reaction so that deposits can be built up
to relatively heavy thicknesses. Specific additions are made to the commercial

solution in order to increase the rate of nickel deposition and also for coating
glass and plastics, should this be desirable. Metals on which the coating does not
deposit include lead, tin solder, cadmium, bismuth, and antimony. The phosphorus
content makes it possible to harden the coating appreciably by low-temperature
heat treatment—for example, 400 °C (750 °F). Corrosion resistance of the nickel–
phosphorus alloy is stated to be comparable to electrolytic nickel in many envi-
ronments. Electroless nickel plating is useful for uniformly coating, with controlled
thickness, the inside surfaces of tubes and other recessed areas [14].
14.3.2 Lead Coatings

Lead coatings on steel are usually formed either by hot dipping or by electrode-
position. In the hot-dipping operation, a few percent tin are usually incorporated
to improve bonding with the underlying steel. When 3–15% tin is incorporated,
the resulting lead–tin alloy is called terne. “Terne,” which means “dull,” was origi-
nally used to differentiate such coatings from bright tin plate. Coatings of lead
or lead–tin alloy are resistant to atmospheric attack, the pores tending to fill with
corrosion product, most likely lead sulfate (PbSO4) which stifles further reaction
[15]. Lead coatings are not very protective in the soil. Lead coatings must not be
used in contact with drinking water or food products, because of the poisonous
nature of small quantities of lead salts (see Section 1.2). Lead and lead–tin coat-
ings are used to enhance the corrosion resistance of iron castings to H2SO3 and
H2SO4 [16].
14.3.3 Zinc Coatings

Coatings of zinc, whether hot-dipped or electroplated, are called galvanized coat-
ings, and the term electrogalvanized is used to differentiate electroplated from
hot-dipped coatings. The electroplating process has been used to explore new
zinc alloy coatings, such as Zn–Fe, Zn–Co, and Zn–Ni [17].
The coating produced by hot dipping is bonded to the underlying steel by a
series of Zn–Fe alloys, with a layer of almost pure zinc on the outside surface.
The coating produced in the batch process is thicker than that produced in the
continuous process, and it has clearly distinguishable alloy layers. The continuous
process results in a thinner coating with a very thin alloy layer at the coating–steel
interface [17].
Zinc coatings are relatively resistant to rural atmospheres and also to
marine atmospheres, except when seawater spray comes into direct contact
with the surface. Table 14.1 lists the ranges of typical atmospheric corrosion
rates in each of the three types of atmospheres, rural, marine, and urban/
industrial [18].
In aqueous environments at room temperature, the overall corrosion rate in
short time tests is lowest within the pH range 7–12 (Fig. 14.3). In acid or very
alkaline environments, the major form of attack results in hydrogen evolution.
TABLE 14.1. Atmospheric Corrosion Rates of Zinc [18]

Type of Atmosphere Range of Corrosion
Rate (μm/year)
Rural 0.2–3
Marine (outside the splash zone) 0.5–8
Urban and industrial 2–16
Figure 14.3. Effect of pH on corrosion of zinc, aerated solutions, 30 °C [B. Roetheli, G. Cox,
and W. Littreal, Metals and Alloys 3, 73 (1932)].
Above about pH 12.5, zinc reacts rapidly to form soluble zincates in accord
with
Zn + OH − + H 2O → HZnO−2 + H 2
In seawater, zinc coatings are effectively resistant for protecting steel against
rusting, with each mil (0.03 mm) of zinc equaling about one year of life; thus, a
coating 5 mils (0.13 mm) thick will protect steel against the appearance of rust
for about five years.
In many aerated hot waters, reversal of polarity between zinc and iron occurs
at temperatures of about 60 °C (140 °F) or above [19–21]. This reversal of polarity
leads to zinc having the characteristics of a noble coating instead of a sacrificial
coating; hence, a galvanized coating under these circumstances can induce pitting
of the base steel.
A 15-year service test on piping carrying Baltimore City water at a mean
temperature of 46 °C (115 °F) and maximum of 80 °C (176 °F) confirmed that
pitting of galvanized pipe was 1.2–2 times deeper than that in black iron pipe
(not galvanized) of the same type, corresponding to shorter life of the galvanized
pipe. In cold water, however, pits in galvanized pipe were only 0.4–0.7 as deep as
those in black iron pipe, indicating, in this case, a beneficial effect of galvanizing
[22]. It was found that waters high in carbonates and nitrates favor the reversal
in polarity, whereas those high in chlorides and sulfates decrease the reversal
tendency [23].
The potential of zinc relative to steel is apparently related to the formation
of porous Zn(OH)2 or basic zinc salts, which are insulators, under those condi-
tions for which zinc is anodic to steel, but is related to formation of ZnO instead
under conditions where the reverse polarity occurs [24]. The latter compound
conducts electronically, being a semiconductor. It can, therefore, perform in
aerated waters as an oxygen electrode, the potential of which, like mill scale on
steel, is noble to both zinc and iron. Accordingly, in deaerated hot or cold waters
in which an oxygen electrode does not function, because oxygen is absent, zinc
is always anodic to iron, but this is not necessarily true in aerated waters. Appar-
ently, the presence of HCO−3 and NO−3, aided by elevated temperatures, stimulates
formation of ZnO, whereas Cl− and SO2− 4 favor formation of hydrated reaction
products instead.
At room temperature, in water or dilute sodium chloride, the current output
of zinc as anode decreases gradually because of insulating corrosion products
that form on its surface. In one series of tests, the current in a zinc–iron couple
decreased to zero after 60–80 days, and a slight reversal of polarity was reported
[25]. This trend is less pronounced with high-purity zinc, on which insulating coat-
ings have less tendency to form.
14.3.4 Cadmium Coatings

Cadmium coatings are produced almost exclusively by electrodeposition. The
difference in potential between cadmium and iron is not as large as that between
zinc and iron; hence, cathodic protection of steel by an overlayer of cadmium
falls off more rapidly with size of coating defects. The lower potential difference
provides an important advantage to cadmium coatings applied to high-strength
steels (Rockwell C > 40, see Section 8.4.1). By maintaining a potential below the
critical potential for S.C.C., but not overlapping the still more active hydrogen
cracking potential range, cadmium coatings, compared to zinc coatings, more
reliably protect the steel against failure by cracking in moist atmospheres.
Cadmium is more expensive than is zinc, but cadmium retains a bright metallic
appearance longer, ensures better electrical contact and solderability, and, con-
sequently, finds use in electronic equipment. Furthermore, it is more resistant to
attack by aqueous condensate and by salt spray. Otherwise, however, cadmium
coatings exposed to the atmosphere are not quite as resistant as zinc coatings of
equal thickness. Because the coefficient of friction of cadmium is less than that
of zinc, cadmium is preferred for fastening hardware and connectors that are
repeatedly taken on and off.
In aqueous media, cadmium, unlike zinc, resists attack by strong alkalies. Like
zinc, it is corroded by dilute acids and by aqueous ammonia. Cadmium salts are
toxic, and, for this reason, cadmium coatings must not come into contact with food
products. Zinc salts are less toxic in this respect, and galvanized coatings are toler-
ated for drinking water, but they also are not recommended for contact with foods.
Applications in which corrosion products of cadmium can enter the environment
must be avoided. Because solutions used for plating cadmium are toxic, disposal
is difficult. Cadmium should be specified only after thorough investigation of the
implications and alternatives [26]. Because of toxicity considerations and regula-
tions concerning use of cadmium and disposal of wastes containing cadmium,
effective cadmium replacements are being identified wherever possible [27].
14.3.5 Tin Coatings

Tinplate is a low-carbon steel strip product coated on both sides with a thin layer
of tin. Several million tons of tinplate are produced each year, and most of it is
used to manufacture many billions of food containers. The nontoxic nature of tin
salts makes tinplate ideal for use with beverages and foods.
Because electrodeposited tin is more uniform than is hot-dipped tin and can
be produced as thinner coatings, tinplate is now produced universally by electro-
deposition. After electroplating the tin on the steel substrate, the tinplate is given
a heating cycle that melts the tin coating, creating a layer of tin–iron intermetallic
compound at the tin–steel interface. The tinplate is then passivated, either in
chromic acid (H2CrO4) or in sodium dichromate (Na2Cr2O7), and, finally, a thin
layer of lubricant is applied. As supplied to the can maker, the typical tinplate
product consists of five layers [28]:
1. Steel sheet approximately 200–300 μm (7.8–11.7 mils) thick

2. On each side, a layer of tin–iron intermetallic compound about 0.08 μm
(0.004 mil) thick
3. Tin layer, 0.3 μm (0.012 mil) thick
4. Passivation film about 0.002 μm (0.00008 mil) thick
5. Oil film about 0.002 μm (0.00008 mil) thick
Tin coatings so thin are, naturally, very porous; hence, it is essential that the tin
act as a sacrificial coating in order to avoid perforation by pitting of the thin-gage
steel on which the tin is applied. This condition usually applies.
On the outside of a tinned container, tin is cathodic to iron, in accord with

the standard potential of tin equal to −0.136 V compared to −0.440 V for iron. On
the inside, however, tin is almost always anodic to iron, and hence, tin cathodically
protects the base steel. This fortunate reversal of potential occurs because stan-
nous ions, Sn2+, are complexed by many food products that greatly reduce Sn2+
activity, resulting in a change in corrosion potential of tin in the active direction
(see Section 3.8). On the inside of the can, the corrosion reaction for tin is
Sn → Sn 2+ + 2e − (14.1)
Two possible reduction reactions are
O2 + 2 H 2O + 4e − → 4OH − (14.2)
and
2 H + + 2e − → H 2 (14.3)
Oxygen inside the can is usually limited to that in the headspace (i.e., the space
between the top of the contents of the can and the lid), so that oxygen reduction
takes place, by reaction (14.2), with accompanying corrosion of the tin, reaction
(14.1), until the oxygen is consumed. Any further corrosion of tin is limited by
the hydrogen evolution reaction (HER). Because tin has high hydrogen overpo-
tential, reduction of hydrogen ions on tin is not significant, where as hydrogen
reduction can occur on the steel substrate. In the absence of other depolarizers,
it is this reaction—reduction of hydrogen on the steel substrate at pores in the
tin coating—that controls detinning. Because the tin coating is the anode, loss of
tin by reaction (14.1) takes place. Corrosion of tin usually proceeds slowly over
the years of useful life of the can. As tin dissolves, more steel may become
exposed, so that both reactions—reduction of hydrogen on the steel and dissolu-
tion of tin—accelerate [29].
In addition to acids or alkalies as incidental and natural components, foods
usually contain various organic substances, some of which are complexing agents,
as mentioned previously, and others act either as corrosion inhibitors or as
cathodic depolarizers. Foods low in inhibitor and high in depolarizer substances
may cause more rapid corrosion of food containers than, for example, highly acid
foods. Because of the presence of organic depolarizers, corrosion of the inside
tin coating of food containers may occur with little or no hydrogen evolution.
When the tin coating has all corroded, however, it is observed that subsequent
corrosion usually occurs by hydrogen evolution. The reason for this behavior is
not firmly established, but it may be related to the fact that Sn2+ ions, which are
known to inhibit corrosion of iron in acids, increase hydrogen overpotential,
thereby favoring reduction of organic substances at the iron cathode. Stannous
ions formed continuously at the iron surface during corrosion of the tin layer do
not maintain sufficient concentration once the tin layer has dissolved. It is also
possible that the potential difference of the iron–tin couple favors adsorption and
reduction of organic depolarizers at the cathode, whereas these processes do not
take place at lower potential differences. Eventual failure of containers is by so-
called hydrogen swells, in which an appreciable pressure of hydrogen builds up
within the can, making the contents suspect, since bacterial decomposition also
causes gas accumulation.
The amount of hydrogen accumulated within the lifetime of the container is
determined not only by the tin coating thickness, the temperature, and the chemi-
cal nature of food in contact, but most often by the composition and structure of
the base steel. The rate of hydrogen evolution is increased by cold working of
the steel (see Section 8.1), which is standard procedure for strengthening the
container walls. Subsequent low-temperature heat treatment, incidental or inten-
tional, may increase or decrease the rate (see Fig. 8.1, Section 8.1).
14.3.5.1 Properties of Tin. Tin is an amphoteric metal, reacting with both

acids and alkalies, but it is relatively resistant to neutral or near-neutral media.
It does not corrode in soft waters and has been used for many years as piping
for distilled water. Only the high price of tin accounts for its replacement for
distilled water piping by other materials, such as aluminum.
Corrosion in dilute nonoxidizing acids, such as HCl and H2SO4, is determined
largely by concentration of dissolved oxygen in the acid. The hydrogen overpo-
tential of tin is so high that corrosion accompanied by hydrogen evolution is
limited. Deaerated acetic acid, for example, either hot or cold, corrodes tin slowly
(1.5–6.0 gmd); NH4OH and Na2CO3 have little effect, but, in concentrated NaOH,
the rate of attack is rapid with formation of sodium stannate. As with acids, the
rate is increased by aeration. In aerated fruit juices at room temperature, rates
are only 0.1–2.5 gmd, but they become more than 10 times higher at the boiling
point, indicating appreciable increase of attack with temperature [30].
14.3.6 Chromium-Plated Steel for Containers

Because of price advantage, steel may be coated with a combined thin chromium
layer (0.3–0.4 μin; 0.008–0.01 μm), followed by chromium oxide (5–40 mg Cr/m2)
and an organic top coat. The advantages include good storage ability, resistance
to sulfide staining, good adhesion, freedom from undercutting of the organic
coating on the inside, and resistance to filiform corrosion on the outside of the
container. However, it is not readily soldered, limiting its use in some application
to can ends.
Chromium (φo = −0.74 V) is more active in the Emf Series than is iron (φo =
−0.44 V), but chromium has a strong tendency to become passive ( φF = 0.2 V).
Hence, the potential of chromium in aqueous media is usually noble to that of
steel. However, in galvanic couples of the two metals, especially in acid media,
chromium is polarized below its Flade potential, so that it exhibits an active
potential. Hence, the corrosion potential of chromium-plated steel, which is
always porous to some degree, is more active than that of either passive
chromium or the underlying steel [31]. Under these conditions, chromium acts as
a sacrificial coating in the same manner as does a tin coating, but with dependence
of its active potential on passive–active behavior rather than on formation of
metal complexes. The metallic chromium layer contributes resistance to under-
cutting of the organic coating.
A chromium oxide coating enhances adhesion of the organic top coating,
with optimum adhesion occurring for a hydrated oxide thickness [32] equivalent
to 20 mg/m2 (2 mg/ft2). The organic coating, in turn, seals pores in the metal
coating, increases resistance to the flow of electric current produced by galvanic
cells, and reduces the amount of iron salts entering the contents of the container
and affecting flavor or color [33].
14.3.7 Aluminum Coatings

Steel is aluminized (i.e., coated with aluminum) by hot dipping or spraying and,
to a lesser extent, by cementation. Molten baths of aluminum for hot dipping
usually contain dissolved silicon in order to retard formation of a brittle alloy
layer. Hot-dipped coatings are used for oxidation resistance at moderately ele-
vated temperatures, such as for oven construction and for automobile mufflers.
They are unaffected by temperatures up to 480 °C (900 °F). At still higher tem-
peratures, the coatings become refractory, but continue to be protective up to
about 680 °C (1250 °F) [34].
The use, since 1975, of catalytic converters in automobiles has resulted in
increased exhaust gas temperatures, up to 870 °C (1600 °F), with metal tempera-
tures up to 760 °C (1400 °F), as well as increased concentrations of corrosive
chemicals, such as sulfuric acid, in the exhaust gas stream. As a result, materials
resistant to high-temperature oxidizing conditions, such as hot dip aluminum-
coated type 409 stainless steel, are being used in automotive exhaust systems
[35–37].
Aluminum coatings are also used for protecting against atmospheric corro-
sion, an application that is limited by higher costs of aluminum compared to zinc
coatings and by variable performance. In soft waters, aluminum exhibits a poten-
tial that is positive to steel; hence, it acts as a noble coating. In seawater and in
some fresh waters, especially those containing Cl− or SO2− 4 , the potential of alu-
minum becomes more active and the polarity of the aluminum–iron couple may
reverse. An aluminum coating under these conditions is sacrificial and cathodi-
cally protects steel. An Al–Zn alloy coating consisting of 44% Zn, 1.5% Si, bal.
Al has been reported to have excellent resistance to marine and industrial atmo-
spheres. It also protects against oxidation at elevated temperatures.
Sprayed coatings are commonly sealed with organic lacquers or paints to
delay eventual formation of visible surface rust. The usual thickness of sprayed
aluminum is 3–8 mils (0.08–0.2 mm). In one series of tests conducted in an indus-
trial atmosphere, sprayed coatings 3 mils (0.08 mm) thick showed an average life
of 12 years in comparison with 7 years for zinc, with the latter coatings being
sprayed, electrodeposited, or hot-dipped [38].
REFERENCES 281
Cemented coatings (“Calorizing”) are produced by tumbling the work in a

mixture of aluminum powder, Al2O3, and a small amount of NH4Cl as flux in a
hydrogen atmosphere at about 1000 °C (1800 °F). An aluminum–iron surface
alloy forms that imparts useful resistance to high-temperature oxidation in air
up to 850–950 °C (1550–1750 °F), as well as resistance to sulfur-containing atmo-
spheres, such as those encountered in oil refining. Cemented aluminum coatings
on steel are not useful for resisting aqueous environments. They are sometimes
used to protect gas turbine blades (nickel-base alloys) from oxidation at elevated
temperatures.
REFERENCES
1. T. J. Langill, in ASM Handbook, Vol. 13A, Corrosion: Fundamentals, Testing, and Pro-
2. T. Mooney, ibid., pp. 772–785.
3. H. E. Townsend, in Automotive Corrosion and Protection, Proceedings of the CORRO-
SION/91 Symposium, NACE International, Houston, TX, 1991, p. 31-1.
4. M. L. Berndt and C. C. Berndt, in ASM Handbook, Vol. 13A, Corrosion: Fundamentals,
5. M. R. Dorfman, in Handbook of Environmental Degradation of Materials, M. Kutz,
editor, William Andrew Publishing, Norwich, NY, 2005, pp. 405–422.
6. G. Carter, Metal Progr. 93, 117 (1968).
7. G. Dearnaley, in Ion Implantation Metallurgy, C. Preece and J. Hirvonen, editor, The
Metallurgical Society of AIME, Warrendale, PA, 1980, pp. 1–20.
8. E. McCafferty, P. G. Moore, J. D. Ayers, and G. K. Hubler, in Corrosion of Metals Pro-
cessed by Directed Energy Beams, C. R Clayton and C. M. Preece, editors, The Metal-
lurgical Society, Warrendale, PA, 1982, pp. 1–21.
9. J. Mazia, D. S. Lashmore, and T. Mooney, in ASM Handbook, Vol. 13A, Corrosion: Fun-
damentals, Testing, and Protection, ASM International, Materials Park, OH, 2003,
p. 780.
10. W. Vernon, J. Inst. Metals 48, 121 (1932).
11. A. R. Jones, in ASM Handbook, Vol. 13, Corrosion, ASM International, Materials Park,
OH, 1987, p. 871.
12. F. LaQue, Trans. Inst. Metal Finishing 41, 127 (1964).
13. A. Brenner and G. Riddell, J. Natl. Bur. Std. (U.S.) 39, 385 (1947).
14. T. Mooney, in ASM Handbook, Vol. 13A, Corrosion: Fundamentals, Testing, and Protec-
tion, ASM International, Materials Park, OH, 2003, p. 777.
15. Ibid., p. 779.
16. T. C. Spence, in ASM Handbook, Vol. 13B, Corrosion: Materials, ASM International,
17. X. G. Zhang, in Uhlig’s Corrosion Handbook, 2nd edition, R. W. Revie, editor, Wiley,
New York, 2000, pp. 888–889.
18. E. Mattsson, Mater. Performance 21(7), 9 (1982).
19. G. Schikorr, Trans. Electrochem. Soc. 76, 247 (1939).

20. G. K. Glass and V. Ashworth, Corros. Sci. 25, 971 (1985).
21. X. G. Zhang, in ASM Handbook, Vol. 13B, Corrosion: Materials, ASM International,
22. C. Bonilla, Trans. Electrochem. Soc. 87, 237 (1945).
23. R. Hoxeng and C. Prutton, Corrosion 5, 330 (1949).
24. P. Gilbert, J. Electrochem. Soc. 99, 16 (1952).
25. H. Roters and F. Eisenstecken, Arch. Eisenhüttenw 15, 59 (1941).
26. Ref. 14, p. 780.
27. M. W. Ingle, Cadmium elimination, in ASM Handbook, Vol. 5, Surface Engineering,
28. ASM Handbook, Vol. 13B, Corrosion: Materials, ASM International, Materials Park,
OH, 2005, p. 186.
29. T. P. Murphy, in Uhlig’s Corrosion Handbook, 2nd edition, R. W. Revie, editor, Wiley,
New York, 2000, pp. 858–860.
30. B. Gonser and J. Strader, in Corrosion Handbook, H. H. Uhlig, editor, Wiley, New York,
1948, p. 327.
31. G. Kamm, A. Willey, and N. Linde, J. Electrochem. Soc. 116, 1299 (1969).
32. M. Vucich, National Steel Corporation, private communication with HHU, 1983.
33. R. McKirahan and R. Ludwigsen, Mater. Prot. 7(12), 29 (1968).
34. Prevention of Corrosion of Motor Vehicle Body and Chassis Components, Society of
Automotive Engineers, Warrendale, PA, 1981.
35. ASM Handbook, Vol. 13, Corrosion, ASM International, Materials Park, OH, 1987,
p. 1016.
36. W. R. Patterson, Materials, design, and corrosion effects on exhaust system life, SAE
Paper 780921, in Designing for Automotive Corrosion Prevention, P-78, Society of
Automotive Engineers, 1978, pp. 71–106.
37. J. Douthett, Automotive Exhaust System Corrosion, in ASM Handbook, Vol. 13C, Cor-
rosion: Environments and Industries, ASM International, Materials Park, OH, 2006,
pp. 519–520.
38. J. Hudson, Chem. Ind. (London) 1961, p. 3 (January 7).
GENERAL REFERENCES
F. E. Goodwin, Lead and lead alloys, in Uhlig’s Corrosion Handbook, 2nd edition, R. W.
S. Grainger and J. Blunt, editors, Engineering Coatings—Design and Application, 2nd edition,
William Andrew Publishing, Cambridge, England, 1998.
G. Krauss and D. K. Matlock, editors, Zinc-Based Steel Coating Systems: Metallurgy and
Performance, TMS, Warrendale, PA, 1990.
Metal coatings, in ASM Handbook, Vol. 13A, Corrosion: Fundamentals, Testing, and Pro-
tection, ASM International, Materials Park, OH, pp. 772–813.
T. P. Murphy, Tin and tinplate, in Uhlig’s Corrosion Handbook, 2nd edition, R. W. Revie,
L. Pawlowski, The Science and Engineering of Thermal Spray Coatings, Wiley, Chichester,
England, 1995.
X. G. Zhang, Zinc, in Uhlig’s Corrosion Handbook, 2nd edition, R. W. Revie, editor, Wiley,
New York, 2000, pp. 887–904.
15
INORGANIC COATINGS
15.1 VITREOUS ENAMELS
Vitreous enamels, glass linings, and porcelain enamels are all essentially glass
coatings of suitable coefficient of expansion fused on metals. Glass in powdered
form (as glass frits) is applied to a pickled or otherwise prepared metal surface,
then heated in a furnace at a temperature that softens the glass and allows it to
bond to the metal. Several coats may be applied. Vitreous enamel coatings are
used mostly on steel, but some coatings are also possible on copper, brass, and
aluminum.
In addition to decorative utility, vitreous enamels protect base metals against
corrosion by many environments. The glasses are composed essentially of alkali
borosilicates and can be formulated to resist strong acids, mild alkalies, or both.
Their highly protective quality results from virtual impenetrability to water and
oxygen over relatively long exposure times, and from their durability at ambient
and above-room temperatures. Their use in cathodically protected hot-water
tanks has already been mentioned in Section 13.4. Although pores in the coating
are permissible when cathodic protection supplements the glass coating, for other
applications the coating must be perfect and without a single defect. This means
that glass-lined vessels for the food and chemical industries must be maintained

285
286 INORGANIC COATINGS
free of cracks and other defects. Susceptibility to mechanical damage and crack-
ing by thermal shock are the main weaknesses of glass coatings. If damage occurs,
repairs can sometimes be made by tamping gold or tantalum foil into the voids.
Enameled steels exposed to the atmosphere last many years when used as
gasoline pump casings, advertising signs, decorative building panels, plumbing
fixtures, appliances, and so on. Failure occurs eventually by formation of a network
of cracks in the coating—called crazing—through which rust appears. Vitreous
enamels are also used to protect against high-temperature gases (e.g., in airplane
exhaust tubes), and they have long life when exposed to soils.
15.2 PORTLAND CEMENT COATINGS
Portland cement coatings have the advantages of low cost, a coefficient of expan-
sion (1.0 × 10−5/°C) approximating that of steel (1.2 × 10−5/°C), and ease of appli-
cation or repair. The coatings can be applied by centrifugal casting (as for the
interior of piping), by troweling, or by spraying. Usual thickness ranges from 5
to 25 mm (0.2–1 in.); thick coatings are usually reinforced with wire mesh.
Portland cement coatings are used to protect cast iron and steel water pipe
on the water or soil side or both, with an excellent record of performance. In
addition, Portland cement coatings are used on the interior of hot- and cold-water
tanks, oil tanks, and chemical storage tanks. They are also used to protect against
seawater and mine waters. The coatings are usually cured for 8–10 days before
exposure to nonaqueous media, such as oils.
A disadvantage of Portland cement coatings is the sensitivity to damage by
mechanical or thermal shock. Open tanks are easily repaired, however, by trowel-
ing fresh cement into cracked areas. There is evidence that small cracks in cold-
water piping are automatically plugged with a protective reaction product of rust
combining with alkaline products leached from the cement. In sulfate-rich waters,
Portland cement may be attacked, but cement compositions are now available
with improved resistance to such waters.
15.3 CHEMICAL CONVERSION COATINGS
Chemical conversion coatings are protective coatings formed in situ by chemical

reaction with the metal surface. They include special coatings, such as PbSO4,
which forms when lead is exposed to sulfuric acid, and iron fluoride, which forms
when steel containers are filled with hydrofluoric acid (>65% HF).
Phosphate coatings on steel (“Parkerizing,” “Bonderizing”) are produced by
brushing or spraying, onto a clean surface of steel, a cold or hot dilute manganese
or zinc acid orthophosphate solution (e.g., ZnH2PO4 plus H3PO4). The ensuing
reaction produces a network of porous metal phosphate crystals firmly bonded
to the steel surface (Fig. 15.1). Accelerators are sometimes added to the phos-
phating solution (e.g., Cu2+, ClO−3 , or NO−3 ) to speed the reaction.
CHEMIC AL CONVERSION COATINGS 287
Figure 15.1. Scanning electron photomicrograph of phosphated type 1010 mild steel; acidic
zinc phosphate + sodium nitrate accelerator applied at 65 °C for 1 min (Symposium on Inter-
face Conversion for Polymer Coatings, edited by P. Weiss and G. Cheever, Elsevier, New York,
1968).
Phosphate coatings do not provide appreciable corrosion protection in them-

selves. They are useful mainly as a base for paints, ensuring good adherence of
paint to steel and decreasing the tendency for corrosion to undercut the paint
film at scratches or other defects. Sometimes, phosphate coatings are impregnated
with oils or waxes, which may provide some protection against rusting, especially
if they contain corrosion inhibitors.
In corrosion-resistant automobile bodies, the first—and probably the most
important—layer of the paint system is the phosphate coating. Although it is the
thinnest coating in the paint system [about 3 μm (0.1 mil) thick], it is the anchor
for the subsequent layers [1].
Oxide coatings on steel can be prepared by controlled high-temperature
oxidation in air or, for example, by immersion in hot concentrated alkali solutions
containing persulfates, nitrates, or chlorates. Such coatings, blue, brown, or black
in color, consist mostly of Fe3O4 and, like phosphate coatings, are not protective
against corrosion. When rubbed with inhibiting oils or waxes, as is often done
with oxidized gun barrels, some protection is obtained.
Oxide coatings on aluminum are produced at room temperature by anodic
oxidation of aluminum (called anodizing) in a suitable electrolyte (e.g., dilute
sulfuric acid) at current densities of 100 or more A/m2. The resultant coating of
Al2O3 may be 0.0025–0.025 mm (0.1–1 mil) thick. The oxide so formed must be
hydrated to improve its protective qualities by exposing anodized articles to
steam or hot water for several minutes, a process called sealing. Improved
288 INORGANIC COATINGS
corrosion resistance is obtained if sealing is done in a hot dilute chromate solu-

tion. The oxide coating may be dyed various colors, either in the anodizing bath
or afterward.
Anodizing provides aluminum with some degree of improved corrosion
resistance, but the additional protection is not spectacular, and it is certainly less
than proportional to oxide thickness. Anodized coatings provide a good base for
paints on aluminum, which is otherwise difficult to paint without special surface
preparation.
Coatings of MgF2 on magnesium can be formed by anodizing the metal at
90–120 V in 10–30% NH4HF2 solution at room temperature. This coating has been
recommended for surface cleaning or as a base for finishing treatments [2].
Chromate coatings are produced on zinc by immersing the cleaned metal for
a few seconds in sodium dichromate solution (e.g., 200 g/liter) acidified with sul-
furic acid (e.g., 8 mL/liter) at room temperature and then rinsing and drying. A
zinc chromate surface is produced that imparts a slight yellow color and that
protects the metal against spotting and staining by condensed moisture. It also
increases the life of zinc to a modest degree on exposure to the atmosphere.
Similar coatings have been recommended for Zn–Al coatings [3] and for cadmium
coatings on steel.
REFERENCES
1. L. L. Piepho, L. Singer, and M. R. Ostermiller, in Automotive Corrosion and Protection,

R. Baboian, editor, NACE International, Houston, TX, 1992, pp. 20–8.
2. E. Emley, Principles of Magnesium Technology, Pergamon Press, New York, 1966.
3. H. Townsend and J. Zoccola, J. Electrochem. Soc. 125, 1290 (1978).
GENERAL REFERENCES
Automotive Corrosion and Protection, R. Baboian, editor, NACE International, Houston,

TX, 1992.
B. Grambow, Corrosion of Glass, in Uhlig’s Corrosion Handbook, 2nd edition, R. W. Revie,
Porcelain enamels, in ASM Handbook, Vol. 13A, Corrosion: Fundamentals, Testing, and
Protection, ASM International, Materials Park, OH, 2003, pp. 750–754.
16
ORGANIC COATINGS
16.1 INTRODUCTION
In the United States, the Clean Air Act has had a major influence on the formula-
tion and application of organic coatings. Solvent vapors from coating operations
undergo photochemical oxidation in the atmosphere and contribute to smog. In
order to reduce this pollution, new coating products, termed compliant coatings,
have been developed with reduced volatile organic compounds. In addition,
alternative processes are now being used in place of the traditional vapor degreas-
ing in which chlorofluorocarbons and 1,1,l-trichloroethane, both being class 1
ozone-depleting chemicals, were used.
16.2 PAINTS
The total value of paints, varnishes, and lacquers produced in the United States
in 2006 amounted to about 21 billion (21 × 109) dollars [1], half of which is esti-
mated to be used for corrosion protection. Painted systems require continued
maintenance to ensure integrity of corrosion protection. For example, in 1995,
the Port Authority of New York and New Jersey began a 20-year, $500 million

289
290 ORGANIC COATINGS
program to repaint all bridges. The existing, lead-based paint was removed by
abrasive blasting down to the bare metal. The new paint system, consisting of
three coats, zinc primer, epoxy intermediate, and urethane finish, is expected to
last 25 years with “moderate maintenance” [2].
Paints are a mixture of insoluble particles of pigment suspended in a continu-
ous organic or aqueous vehicle. Pigments usually consist of metallic oxides (e.g.,
TiO2, Pb3O4, Fe2O3) or other compounds, such as ZnCrO4, PbCO3, BaSO4, clays,
and so on. The vehicle may be a natural oil—linseed or tung oil, for example.
When these drying oils are exposed to air, they oxidize and polymerize to solids,
a process that can be hastened by small amounts of catalysts, such as lead, man-
ganese, or cobalt soaps. Synthetic resins are now more often used as vehicles or
components of vehicles, particularly for continuous contact with water or where
resistance to acids, alkalies, or higher temperatures is required. These resins may
dry by evaporation of the solvent in which they are dissolved, or they may poly-
merize through application of heat or by addition of catalysts. Varnishes consist
generally of a mixture of drying oil, dissolved resins, and a volatile thinner. Lac-
quers consist of resins dissolved in a volatile thinner; they sometimes contain
pigments as well. Because of the need to reduce atmospheric pollution, use of
aqueous vehicle paints is preferred, and in some cities required, over use of paints
employing volatile organic solvents.
Examples of synthetic resins include phenol-formaldehyde formulations,
which withstand boiling water or slightly higher temperatures and are used in
the chemical industry in the form of multiple coats, baked on, for resisting a
variety of corrosive media. Silicone and polyimide resins are useful at still higher
temperatures. Alkyd resins, because of favorable cost, fast-drying properties, and
durability, have found wide application for protecting the metal surfaces of
machinery and home appliances.
Vinyl resins have good resistance to penetration by water. Their resistance
to alkalies makes them useful for painting structures that are to be protected
cathodically. Linseed- and tung-oil paints, by comparison, are quickly saponified
and disintegrated by alkaline reaction products formed at a cathode, whether in
waters or in soil.
Epoxy resins are also resistant to alkalies and to many other chemical media
and have the distinguishing property of adhering well to metal surfaces. The latter
property presumably derives from many available polar groups in the molecule.
These resins are the basis of plastic mixtures that, on addition of a suitable cata-
lyst, solidify in place within a short time. They are useful, for example, to seal
leaks temporarily in ferrous or nonferrous piping.
Paints, in general, are not useful for protecting buried structures, one reason
being that mechanical damage to thin coatings by contact with the soil is difficult
to avoid. Tests have shown that, for this purpose, their life is relatively short.
Coatings based on coal tar or on fusion-bonded epoxy have been found to be far
more practical. Similarly, the usual linseed-tung oil paints are not durable for
metal structures totally immersed in water, except possibly for short periods of
time on the order of one year or less. In hot water, life is still shorter. More ade-
REQUIREMENTS FOR CORROSION PROTECTION 291
quate protection extending up to several years at ordinary temperatures can be

obtained by applying four or five coats of a synthetic vehicle paint, as is done in
the chemical industry. Because of the expense of a multiple-coat system of this
kind, many applications for fresh water or seawater make use, instead, of thick
coal-tar coatings. By far the majority of paints perform best for protecting metals
against atmospheric corrosion, and this is their main function.
16.3 REQUIREMENTS FOR CORROSION PROTECTION
To protect against corrosion, a good paint should meet the following

requirements:
1. Provide a Good Vapor Barrier. All paints are permeable, in some degree,
to water and oxygen. Some vehicles are less permeable than others, but their
better performance as a diffusion barrier applies only to well-adhering multiple-
coat applications that effectively seal pores and other defects. The diffusion path
through a paint film is normally increased by incorporating pigments. Particularly
effective in this regard are pigments having the shape of flakes oriented parallel
(e.g., by brushing) to the metal surface (e.g., micaceous or flaky hematite, alumi-
num powder). Diffusion, on the other hand, tends to be accelerated by electro-
osmosis whenever the coated metal is made the cathode of a galvanic couple or
is cathodically protected.
2. Inhibit against Corrosion. Pigments incorporated into the prime coat (the
coat immediately adjacent to the metal) should be effective corrosion inhibitors.
Water reaching the metal surface then dissolves a certain amount of pigment,
making the water less corrosive. Corrosion-inhibiting pigments must be soluble
enough to supply the minimum concentration of inhibiting ions necessary to
reduce the corrosion rate, yet not soluble to a degree that they are soon leached
out of the paint.
Among pigments that have been recommended for prime coats, only rela-
tively few actually do the job that is required. Effective pigments for which per-
formance has been established in many service tests include (1) red lead (Pb3O4)
having the structure of plumbous ortho-plumbate (Pb2PbO4) and (2) zinc chro-
mate (ZnCrO4) and basic zinc chromate or zinc tetroxychromate. The inhibiting
ion in the case of red lead is probably PbO4− 4 , which is released in just sufficient
amounts to passivate steel, protecting it against rusting by water reaching the
metal surface. It is likely that lead oxides and hydroxides of other compositions
also have inhibiting properties in this regard, but red lead appears to be best of
the lead compounds.
For zinc chromate, the inhibiting ion is CrO2−4 , solubility relations being just
right to release at least the minimum concentration of the ion (>10−4 mole/liter)
for optimum inhibition of steel. The solubility of zinc tetroxychromate is reported
to be 2 × 10−4 mole/liter [3]. Lead chromate, on the other hand, is not nearly
soluble enough (solubility = 1.4 × 10−8 mole/liter) and acts only as an inert
pigment. Commercial formulations of lead chromate sometimes contain lead
oxides, present either inadvertently or intentionally, which may impart a degree
of inhibition.
Zinc molybdate has been suggested as an inhibiting pigment for paints [4],
being white instead of the characteristic yellow of chromates. It is less toxic
than chromates. The sulfate and chloride content of a commercial ZnCrO4
(or ZnMoO4) pigment must be low so that it can passivate the metal surface.
Because inhibiting pigments passivate steel, they are relatively ineffective for
this purpose in the presence of high concentrations of chlorides, such as in
seawater.
Paints pigmented with zinc dust using essentially an aqueous sodium silicate
vehicle (called inorganic zinc-rich paint), or an organic vehicle, are also useful as
prime coats, the function of the zinc being to cathodically protect the steel in the
same manner as galvanized coatings. Such paints are sometimes used over partly
rusted galvanized surfaces because they also adhere well to zinc, but rust should
first be removed. Sacrificial protection by zinc-rich coatings requires intimate
contact with the substrate, and so these coatings are always used as primers. It
has been reported [5] that in order to ensure good electrical contact between zinc
particles and with the base metal, the amount of pigment in the dried paint film
should account for 95% of its weight. A coating of this kind protected steel in
seawater against rusting at a scratch for 1–2 years, whereas with 86% and 91%
Zn, rust appeared after 1–2 days and 10–20 days, respectively. Vehicles for zinc-
rich paints to accommodate such a large fraction of pigment include chlorinated
rubber, polystyrene, epoxy, and polyurethane.
The minimum amount of zinc dust pigment required to provide cathodic
protection depends on several factors, including Zn particle size, nature of the
vehicle, and the amount of ZnO and other pigments that may be present [6]. It
probably also depends on the extent to which insulating coatings form on zinc
particles before the paint is applied (age of paint).
3. Provide Long Life at Low Cost. A reasonable cost of paint should be

gauged by its performance. A paint system lasting 5 years justifies double the cost
of paint if the more expensive paint provides 35% longer life or lasts short of 7
years (labor to paint cost ratio of 2 : 1).
The rate of deterioration of a paint depends on the particular atmosphere to
which it is exposed, which, in turn, depends on the amount of atmospheric pol-
lution and on the amount of rain and sunshine. The color of the top coat (i.e., its
ability to reflect infrared and ultraviolet radiation) and the type of vehicle used
play some part. Other things being equal, the performance of good-quality paints
used for corrosion protection is largely determined by the thickness of the final
paint film. In achieving a given coating thickness, it is advantageous to apply
several coats rather than one, probably because pores are better covered by
several applications and also because evaporation or dimensional changes during
polymerization are better accommodated by thin films.
METAL SURFACE PREPAR ATION 293
16.4 METAL SURFACE PREPARATION
Many test results and a great deal of engineering data over many years have
shown that the most important single factor influencing the life of a paint is the
proper preparation of the metal surface. This factor is, generally, more important
than the quality of the paint that is applied. In other words, a poor paint system
on a properly prepared metal surface usually outperforms a better paint system
on a poorly prepared surface. A well-prepared surface is the foundation on which
the paint system is built.
Adequate surface preparation consists of two main processes.
16.4.1 Cleaning All Dirt, Oils, and Greases from the Surface
Initial cleaning can be accomplished by using solvents or alkaline solutions.
Solvents. Mineral spirits, naphtha, alcohols, ethers, chlorinated solvents, and

so on, are applied by dipping, brushing, or spraying. One such solvent is Stoddard
solvent, a petroleum base mineral spirit with a flash point of 40–55°C
(100–130°F), sufficiently high to minimize fire hazard, and it is not particularly
toxic.
Chlorinated solvents, on the other hand, although nonflammable, are
relatively toxic and contribute to pollution. In addition, they may leave chloride
residues on the metal surface that can later initiate corrosive attack. They are
used largely for vapor degreasing (tri- or perchlorethylene), in which the
work is suspended in the vapor of the boiling solvent. Care must be exercised in
the vapor degreasing of aluminum, ensuring that adequate chemical inhibitors
are added and maintained in the chlorinated solvent in order to avoid cata-
strophic corrosion (see Section 21.1.4.1) or, in the extreme, to avoid an explosive
reaction.
Alkaline Solutions. Aqueous solutions of certain alkalies provide a method

of removing oily surface contamination that is cheaper and less hazardous than
the use of solvents. They are more efficient in this particular function than sol-
vents, but perhaps less effective for removing heavy or carbonized oils. Suitable
solutions contain one or more of the following substances: Na3PO4, NaOH,
Na2O·nSiO2, Na2CO3, borax, and sometimes sodium pyro- or metaphosphate and
a wetting agent. Cleaning may be done by immersing the work in the hot solution
[80°C (180°F) to b.p.] containing about 30–75 g/liter (4–10 oz/gal) alkali. The hot
solution, in somewhat more dilute concentration, may also be sprayed onto the
surface. Electrolytic cleaning in alkaline solutions is also sometimes used; this
process makes use of the mechanical action of hydrogen gas and the detergent
effect of released OH− at the surface of the work connected as cathode to a source
of electric current.
If the metal is free of mill scale and rust, a final rinse in water and in a dilute
chromic–phosphoric acid ensures both removal of alkali from the metal surface,
which would otherwise interfere with good bonding of paint, and also temporary
protection against rusting.
16.4.2 Complete Removal of Rust and Mill Scale

Rust and mill scale are best removed by either pickling or sandblasting.
Pickling. The metal, cleaned as described previously, is dipped into an acid

(e.g., 3–10% H2SO4 by weight) containing a pickling inhibitor (see Section 17.3)
at a temperature of 65–90°C (150–190°F) for an average of 5–20 min. Oxide next
to the metal surface is dissolved, loosening the upper Fe3O4 scale. Sometimes,
sodium chloride is added to the sulfuric acid, or HCl alone is used at lower tem-
peratures, or a 10–20% H3PO4 is used at temperatures up to 90°C (190°F). The
latter acid is more costly, but has the advantage of producing a phosphate film
on the steel surface that is beneficial to paint adherence. Some pickling proce-
dures, in fact, call for a final rinse in dilute H3PO4 in order to ensure removal
from the metal surface of residual chlorides and sulfates that are damaging to
the life of a paint coating.
Sometimes, the final dip is a dilute solution of chromic (30–45 g/liter; 4–6 oz/
gal) or chromic–phosphoric acid, which serves to prevent rusting of the surface
before the prime coat is applied. Use of chromates is less popular than formerly
because their toxicity places restrictions on disposal of spent solutions. Hexava-
lent chromium (Cr6+) is a potent human toxin and known cancer-causing agent
[7]. A relatively nontoxic pickle for steel consists of hot 3–10% ammoniated citric
acid followed by a dilute alkaline sodium nitrite solution to minimize superficial
rusting before application of paint [8].
Blasting. Using this procedure, scale is removed by high-velocity particles

impelled by an air blast or by a high-velocity wheel. Blast materials usually
consist of sand, or sometimes of steel grit, silicon carbide, alumina, refractory slag,
or rock wool byproducts.
Other methods of removing mill scale include flame cleaning, by which scale
spalls off the surface through sudden heating of the surface with an oxyacetylene
torch. Weathering for several weeks or months is also possible; the natural rusting
of the surface dislodges scale, which can then be further removed by wire brush-
ing. But these procedures are less satisfactory than complete removal of scale
and rust by pickling or blasting.
The poor performance of paints on weathered steel exposed to an industrial
atmosphere was shown in tests reported by Hudson [9] (Table 16.1). The rela-
tively long life of paint shown for intact mill scale would probably not be achieved
in actual service. It would, for example, be difficult to keep large areas and various
shapes of mill scale from cracking before or after painting. Fragmentation of mill
scale allows paint to become dislodged, particularly after electrolytic action has
occurred between metal and scale by aqueous solutions that have penetrated to
the metal surface.
APPLYING PAINT COATINGS 295
TABLE 16.1. Effect of Surface Preparation of Steel on Life of Paint Coatings [9]
Surface Preparation Durability of Paint (years) in Sheffield, England
2 Coats Red Lead + 2 Coats 2 Coats Red Iron

Red Iron Oxide Paint Oxide Paint
Intact mill scale 8.2 3.0

Weathered and wire-brushed 2.3 1.2
Pickled 9.5 4.6
Sandblasted 10.4 6.3
16.5 APPLYING PAINT COATINGS
The prime coat should be applied to the dry metal surface as soon as possible
after the metal is cleaned in order to achieve a good bond. Better still, the metal
should first be given a phosphate coat (see Section 15.3), in which case the prime
coat, if necessary, can be delayed for a short while. The advantages of a phosphate
coat are a better bond of paint to metal and good resistance to undercutting of
the paint film at scratches or other defects in the paint at which rust forms and
progresses beneath the organic coating. For many years it has been standard
practice to coat automobile bodies and electric appliances with phosphate before
painting.
Only in unusual cases should paint be applied over a damp or wet surface
because poor bonding of paint to steel results under these conditions. A second
prime coat can be applied after the first has dried, or a sequence of top coats can
follow. A total of four coats with combined thickness of not less than about
0.13 mm (5 mils) is considered by some authorities to be the recommended
minimum for steel that will be exposed to corrosive atmospheres [10].
During the past 30 years, there have been vast improvements in the corrosion
performance of automobiles, driven not only by the demands of the public for
increased corrosion resistance, but also by the Clean Air Act of 1970 [with regula-
tions regarding volatile organic content (VOC)] and subsequent revisions. Tougher
and thicker materials have been developed, and the application processes have
been improved. One of the most important advances has been the development
of the cathodic electrodeposition priming process, introduced in 1976 and, by 1985,
fully implemented by most vehicle manufacturers in their assembly plants. Today,
nearly 100% of the cars and trucks manufactured in the world are primed using
the cathodic electrodeposition process [11]. Following phosphate pretreatment,
the vehicle is immersed in the electrodeposition bath for typically 2–3 minutes
[11]. Electric current is applied, and a film is deposited.
One of the advantages of this process, compared to spraying, for example, is
that it results in a uniform, thin coating [about 25 μm (1 mil) thick] with coverage
on both exterior and interior cavity surfaces. In addition, this process is control-
lable, automated, efficient, and environmentally acceptable [12].
16.5.1 Wash Primer

A wash primer, WP1, was developed during World War II in order to facilitate
the painting of aluminum. Subsequently, it was also found advantageous as a
prime coat for steel and several other metals. One wash primer solution consists
of approximately 9% polyvinyl butyral and 9% zinc tetroxychromate by weight
in a mixture of isopropanol and butanol as one solution, which, just before using,
is mixed with a solution of 18 wt.% H3PO4 in isopropanol and water in the weight
ratio of four of the pigmented solution to one of the latter [13]. The mixture must
be used within 8–24 h after mixing. It has the advantage of providing in one
operation, instead of two, a phosphating treatment of the metal and the applica-
tion of the prime coat. It has proved to be an effective prime coat on steel, zinc
(galvanized steel), and aluminum.
16.5.2 Painting of Aluminum and Zinc

Paints do not adhere well to aluminum without special surface treatment, unless
the wash primer is used, which provides its own surface treatment. Otherwise,
phosphating or anodizing is suitable. The prime coat should, in general, contain
zinc chromate as an inhibiting pigment. Red lead is not recommended, because
of the galvanic interaction of aluminum with metallic lead deposited by replace-
ment of lead compounds. Paints pigmented with zinc dust plus ZnO (zinc-rich
paints) can also be used satisfactorily as a prime coat, forming a good bond with
the metal. In this case, Zn and ZnO apparently react beforehand with organic
acids of the vehicle, ensuring that aluminum soaps and other compounds do not
form at the paint–metal interface to weaken the attachment of paint to metal.
Zinc or galvanized surfaces are also difficult to paint and should be phos-
phated beforehand, or a wash primer should be used as a prime coat. As with
aluminum, zinc chromate, but not red lead, is a suitable inhibiting pigment in the
prime coat, or zinc-rich paints can be used. A coating system consisting of painted
galvanized steel provides a protective service life up to 1.5 times that predicted
by adding the expected lifetimes of the paint and the galvanized coating in a
severe atmosphere, and the synergistic improvement is greater for mild environ-
ments [14].
16.6 FILIFORM CORROSION
Metals with organic coatings may undergo a type of corrosion resulting in numer-
ous meandering thread-like filaments of corrosion product. This is sometimes
known as underfilm corrosion, and it was called filiform corrosion by Sharmon
[15] (Fig. 16.1). It has been described by several investigators and reproduced in
the laboratory [16]. According to reported descriptions, the filaments, or threads,
on steel are typically 0.1–0.5 mm wide. The thread itself is red in color, character-
istic of Fe2O3, and the head is green or blue, corresponding to the presence of
(a)
(b)
Figure 16.1. Filiform corrosion. (a) Lacquered tin can. 1×. (b) Clear varnish on steel, 10× (86%
R.H., 840 h). [Reprinted with permission, M. Van Loo, D. Laiderman, and R. Bruhn, Corrosion
9, 279 (1953). Copyright NACE International 1953.]
ferrous ions. Each thread grows at a constant rate of about 0.4 mm/day in random
directions, but threads never cross each other. If a head approaches another
thread, it either glances off at an angle or stops growing.
Filiform corrosion occurs independent of light, metallurgical factors in the
steel, and bacteria. Although threads are visible only under clear lacquers or
varnishes, they probably also occur under opaque paint films. They have been
observed under various types of paint vehicles and on various metals, including
steel, zinc, aluminum, magnesium, and chromium-plated nickel. This type of cor-
rosion takes place on steel only in air of high relative humidity (e.g., 65–95%).
At 100% relative humidity, the threads may broaden to form blisters. They may
not form at all if the film is relatively impermeable to water, as is stated to be
the case for paraffin [17]. The mechanism appears to be a straightforward example
of a differential aeration cell.
16.6.1 Theory of Filiform Corrosion

Various schematic views of a filiform thread or filament are shown in Fig. 16.2.
The head is made up of a relatively concentrated solution of ferrous salts, as was
shown by analysis [17]. Hence, water tends to be absorbed from the atmosphere
in this region of the thread. Oxygen also diffuses through the film and reaches
higher concentrations at the interface of head and body and at the periphery of
the head, compared to lower concentrations in the center of the head. This sets
up a differential aeration cell with the cathode and accumulation of OH− ions in
all regions where the film makes contact with the metal, as well as at the rear of
the head. The anode is located in the central and forward portions of the head
attended by formation of Fe2+.* The liberated OH− ions probably play an impor-
tant role in undermining the film in view of the well-known ability of alkalies to
destroy the bond between paints and metals (cathodic delamination). In addition,
they diffuse toward the center of the head, reacting with Fe2+ to form FeO·nH2O,
which, in turn, is oxidized by O2 to Fe2O3·nH2O. The precipitated oxide assumes
a typical V shape because more alkali is produced in the region between the head
and the body (more O2), compared to the periphery of the head. Behind the V-
shaped interface, Fe2O3 exists predominantly, and, since it is less hygroscopic than
ferrous salt solutions, water again diffuses out through the film, leaving this
portion relatively dry. Oxygen continues to diffuse through the film, serving to
keep the main portion of the filament cathodic to the head.
If a head should approach another filament body, the previous participation
of the film in filiform growth will have depleted the film of organic and inorganic
anions necessary to the accumulation of high concentrations of ferrous salts in
the head and also of cations necessary to build up a high pH at the periphery.
*The accumulation of alkali at the periphery can be demonstrated by placing a large drop of dilute
sodium chloride solution (1–5%), preferably deaerated, containing a few drops of phenolphthalein
and about 0.1% K3Fe(CN)6 on an abraded surface of iron. Within a few minutes, the periphery turns
pink and the center turns blue
PL ASTIC LININGS 299
Figure 16.2. Schematic views of filiform filament on iron showing details of differential
aeration cell causing attack.
This serves to discourage further growth of the filament in the direction of the
old filament. Furthermore, and perhaps more important, the previous accumula-
tion of OH− added to that being formed, plus still greater abundance of oxygen,
tends to ensure that the old filament body remains cathodic, encouraging the
approaching anode to veer off in another direction. If the head should lose its
electrolyte because of delaminated film at the old thread which it approaches,
the filament would stop growing, a situation sometimes observed.
Phosphate surface treatments and chromate prime coats of paint serve to
limit filiform corrosion, but apparently do not prevent its occurrence. Wholly
adequate remedies have not yet been found.
16.7 PLASTIC LININGS
Protection against acids, alkalies, and corrosive liquids and gases in general can
be obtained by bonding a thick sheet of plastic or rubber to a steel surface.
Rubber, Neoprene, and vinylidene chloride (Saran) are examples of materials

that are so used. A thickness of 3 mm ( 81 in.) or more ensures a relatively good
diffusion barrier and protects the base metal against attack for a long time. The
expense of such coatings usually excludes their use for any but severely corrosive
environments, such as are common in the chemical industry.
Plastic coatings of vinyl or polyethylene can be applied as an adhesive tape,
particularly to protect buried metal structures. Such tape finds practical use for
coating pipe and auxiliary equipment, including pipe connections and valves,
exposed to the soil. However, tape can become disbonded with time, leaving the
pipe uncoated, not cathodically protected since the tape material is nonconduc-
tive, and in contact with the groundwater that leaks into such disbondments. This
sequence of events has resulted in failure by S.C.C. of some underground high-
pressure oil and natural gas pipelines [18].
One of the most stable plastics in terms of resisting a wide variety of chemical
media is tetrafluorethylene (Teflon). It successfully resists aqua regia and boiling
concentrated acids, including HF, H2SO4, and HNO3. It resists concentrated
boiling alkalies, gaseous chlorine, and all organic solvents up to about 250°C
(480°F). It is said to react only with elementary fluorine and with molten sodium.
Slow decomposition into HF and fluorinated hydrocarbons begins at tempera-
tures above 200°C (400°F), with the mixture of gases being highly toxic [19].
Toxic gases may also be liberated by heat generated during machining of the
plastic.
As a material, Teflon is not strong, tending to creep readily under stress. Its
extreme inertness makes bonding to any surface difficult. This compound is used,
typically, for linings, gasket material, and diaphragm valves.
REFERENCES
1. Bureau of Census, U.S. Dept. Of Commerce, Paint and Allied Products: 2006, Table 1,
Current Industrial Report MA325F(06)-1, Washington, D.C., issued June 2007.
2. Port Authority of New York and New Jersey website: http://www.panynj.gov/
CommutingTravel/bridges/html/painting.html
3. P. Nylen and E. Sunderland, Modern Surface Coatings, Interscience, New York, 1965,
(p. 689.)
4. Chem. Eng. News, November 14, 1960, p. 58.
5. J. Mayne, Br. Corros. J. 5, 106 (1970).
6. T. Ross et al., Corros. Sci. 18, 505 (1978).
7. P. Lay and A. Levina, J. Am. Chem. Soc. 120, 6704 (1998).
8. W. Blume, Mater. Perf. 16(3), 18 (1977).
9. J. Hudson, J. Iron Steel Inst. 168, 153 (1951); (with W. Johnson), ibid. 168, 165 (1951).
10. J. Hudson, Chem. Ind. (London) 55, 3 (1961).
11. L. L. Piepho, L. Singer, and M. R. Ostermiller, In Automotive Corrosion and Protection,
R. Baboian, editor, NACE International, Houston, TX, 1992, pp. 20–9, 20–20.
12. John J. Vincent, in Automotive Corrosion and Protection, R. Baboian, editor, NACE
International, Houston, TX, 1992, pp. 21-2–21-3.
13. L. Whiting, Corrosion 15, 311t (1959).
14. T. J. Langill, in ASM Handbook, Vol. 13A, Corrosion: Fundamentals, Testing, and Pro-
15. C. Sharmon, Nature, 153, 621 (1944); Chem. Ind. (London) 46, 1126 (1952).
16. C. Hahin and R. G. Buchheit, In ASM Handbook, Vol. 13A, Corrosion: Fundamentals,
17. W. Slabaugh and M. Grotheer, Eng. Chem. 46, 1014 (1954).
18. Public Inquiry Concerning Stress Corrosion Cracking on Canadian Oil and Gas Pipe-
lines, Report of the Inquiry, Report MH-2-95, National Energy Board, Calgary, Alberta,
November 1996.
19. Bulletin, M.I.T. Occupational Medical Service, December 1961.
GENERAL REFERENCES
A. Forsgren, Corrosion Control through Organic Coatings, CRC Press, Taylor & Francis,
Boca Raton, FL, 2006.
C. H. Hare, Corrosion control of steel by organic coatings, in Uhlig’s Corrosion Handbook,
P. R. Khaladkar, Using plastics, elastomers, and composites for corrosion control, in Uhlig’s
965–1022.
R. Norsworthy, Selection and use of coatings for underground or submersion service, in
pp. 1041–1059.
D. J. Smukowski, Environmental regulation of surface engineering, in ASM Handbook,
Vol. 5, Surface Engineering, ASM International, Materials Park, OH, 1994, pp.
911–917.
K. B. Tator, Organic coatings and linings, in ASM Handbook, Vol. 13A, Corrosion: Funda-
mentals, Testing, and Protection, ASM International, Materials Park, OH, 2003, pp.
817–833.
K. B. Tator, Paint systems, in ASM Handbook, Vol. 13A, Corrosion: Fundamentals, Testing,
and Protection, ASM International, Materials Park, OH, 2003, pp. 837–844.
B. Thomson and R. P. Campion, Testing of polymeric materials for corrosion control, in
pp. 1151–1164.
17
INHIBITORS AND PASSIVATORS
17.1 INTRODUCTION
An inhibitor is a chemical substance that, when added in small concentration to

an environment, effectively decreases the corrosion rate. There are several classes
of inhibitors, conveniently designated as follows: (1) passivators, (2) organic
inhibitors, including slushing compounds and pickling inhibitors, and (3) vapor-
phase inhibitors.
Passivators are usually inorganic oxidizing substances (such as chromates,
nitrites, and molybdates) that passivate the metal and shift the corrosion poten-
tial several tenths volt in the noble direction. Nonpassivating inhibitors, such as
the pickling inhibitors, are usually organic substances that have only slight effect
on the corrosion potential, changing it either in the noble or active direction
usually by not more than a few milli- or centivolts. In general, the passivating-
type inhibitors reduce corrosion rates to very low values, being more efficient in
this regard than most of the nonpassivating types. They represent, therefore, the
best inhibitors available for certain metal–environment combinations. Except
where noted, the discussion in this chapter pertains to steel.
The practice of corrosion inhibition is greatly influenced by new regulations
that have been developed because of toxicity and environmental effects resulting

303
304 INHIBITORS AND PASSIVATORS
from industrial effluents. For example, there is a trend to replace some widely
used inhibitors, especially those that contain hexavalent chromium, Cr6+, a known
carcinogen, in applications where toxicity, environmental damage, and pollution
caused by these chemicals are important considerations.
17.2 PASSIVATORS
17.2.1 Mechanism of Passivation

The theory of passivators has already been discussed in part, and should be
referred to again, in Section 6.3. Passivators in contact with a metal surface act
as depolarizers, initiating high current densities that exceed icritical for passivation
at residual anodic areas. Only those ions can serve as passivators that have both
an oxidizing capacity in the thermodynamic sense (noble oxidation–reduction
potential) and that are readily reduced (shallow cathodic polarization curve), as
−
illustrated in Fig. 17.1. Hence, SO2−4 or ClO4 ions are not passivators for iron,
because they are not readily reduced, nor are NO−3 ions compared to NO−2 ,
because nitrates are reduced less rapidly than are nitrites, with the former reduc-
ing too sluggishly to achieve the required high value of icritical. The extent of
chemical reduction on initial contact of a passivator with metal, according to this
viewpoint, must be at least chemically equivalent to the amount of passive film
Figure 17.1. Polarization curves that show effect of passivator concentration on corrosion
of iron. An oxidizing substance that reduces sluggishly does not induce passivity (dotted
cathodic polarization curve) (schematic).
PASSIVATORS 305
formed as a result of such reduction. For the passive film on iron, as has been
discussed earlier, this is on the order of 0.01 C/cm2 (100 C/m2) of apparent surface
area. The total quantity of equivalents of chemically reduced chromate is found
to be of this order, and it is probably also the same for other passivators acting
on iron. The amount of chromate reduced in the passivation process was arrived
at from measurements [1] of residual radioactivity of a washed iron surface after
exposure to a chromate solution containing radioactive 51Cr. The following reac-
tion applies, assuming that all reduced chromate (or dichromate) remains on the
metal surface as adsorbed Cr3+ or as hydrated Cr2O3:
Cr2O72− + 8 H + + Fesurface → 2Cr 3+ + 4 H 2O + O2 ⋅ Oads on Fe ΔG = −406 kJ
Residual radioactivity accounts for 3 × 1016 Cr atoms/cm2 (1.5 × 10−7 eq or 0.015 C

passive-film substance/cm2). The equation assumes an adsorbed passive-film
structure, but the same reasoning applies whatever the structure.
Reduction of passivator continues at a low rate after passivity is achieved,
equivalent in the absence of dissolved oxygen to the value of ipassive [<0.3 μA/cm2
(<3 mA/m2)] based on observed corrosion rates of iron in chromate solutions.
Iron oxide and chromate reduction products slowly accumulate. The rate of
reduction increases with factors that increase ipassive, such as higher H+ activity,
higher temperatures, and the presence of Cl−. It is found, in practice, that less
chromate is consumed as exposure time continues, consistent with ipassive that also
decreases with time.
For optimum inhibition, the concentration of passivator must exceed a
certain critical value. Below this concentration, passivators behave as active
depolarizers and increase the corrosion rate at localized areas, such as pits. Lower
concentrations of passivator correspond to more active values of the oxidation–
reduction potential, and eventually the cathodic polarization curve intersects the
anodic curve in the active region instead of in the passive region alone (Fig.
17.1).
− −3
The critical concentration for CrO2− 2− 2−
4 , NO2 , MoO4 , or WO4 is about 10 to
−4 −3
10 M [2–5]. A concentration of 10 M Na2CrO4 is equivalent to 0.016% or
160 ppm. Chloride ions and elevated temperatures increase icritical as well as ipassive,
thereby raising the critical passivator concentration to higher values as well. At
70–90°C, for example, the critical concentration of CrO2− 4 and NO−2 is about
−2
10 M [4, 5]. Should the passivator concentration fall below the critical value in
stagnant areas (e.g., at threads of a pipe or in crevices), the active potential at
such areas in galvanic contact with passive areas elsewhere of noble potential
promotes localized corrosion, or pitting, at the active areas through the action of
passive–active cells. For this reason, it is important to maintain the concentration
of passivators above the critical value at all portions of the inhibited system by
stirring, rapid flow rates, and avoiding crevices and surface films of grease and
dirt. Since consumption of passivators increases in the presence of chloride and
sulfate ions, it is also essential to maintain as low a concentration of these ions
as possible.
Some substances indirectly facilitate passivation of iron (and probably of

some other metals as well) by making conditions more favorable for adsorption
of oxygen. In this category are alkaline compounds (e.g., NaOH, Na3PO4,
Na2O · nSiO2, Na2B4O7). These are all nonoxidizing substances requiring dis-
solved oxygen in order to inhibit corrosion; hence, oxygen is properly considered
the passivating substance. The mechanism of passivation is similar to that
described in Sections 7.2.1.3 and 7.2.3. High concentrations of OH− displace H
adsorbed on the metal surface, thereby decreasing the probability of a reaction
between dissolved O2 and adsorbed H. The excess oxygen is then available to
adsorb instead, producing passivity. In addition to passive films of this kind,
protection is supplemented by diffusion-barrier films of iron silicate, iron phos-
phate, and so on.
Passivation of iron by molybdates and tungstates, both of which inhibit in
the near-neutral pH range, requires dissolved oxygen [6], contrary to the situa-
tion for chromates and nitrites. In this case, dissolved oxygen may help create
just enough additional cathodic area to ensure anodic passivation of the remain-
ing restricted anode surface at the prevailing rate of reduction of MoO2− 4 or of
WO2− 4 , whereas in the absence of O , i
2 critical is not achieved.
Sodium benzoate [6, 7] (C6H5COONa), sodium cinnamate [8] (C6H5 · CH ·
CH · COONa), and sodium polyphosphate [9, 10] (NaPO3)n (Fig. 17.2) are further
examples of nonoxidizing compounds that effectively passivate iron in the near-
neutral range, apparently through facilitating the adsorption of dissolved oxygen.
As little as 5 × 10−4 M sodium benzoate (0.007%) effectively inhibits steel in
aerated distilled water [11], but inhibition is not observed in deaerated water.
The steady-state corrosion rate of iron in aerated 0.01 M (0.14%) sodium benzo-
ate, pH 6.8, is only 0.001 gmd, whereas in deaerated solution the rate is 0.073 gmd.
Inhibition occurs only above about pH 5.5; below this value the hydrogen evolu-
tion reaction, for which benzoate ions have no inhibiting effect, presumably
becomes dominant, and the passive film of oxygen is destroyed.
Gatos [12] found that optimum inhibition of steel in water of pH 7.5 contain-
ing 17 ppm NaCl occurred at and above 0.05% sodium benzoate or 0.2% sodium
cinnamate. By using radioactive 14C as tracer, only 0.07, 0.12, and 0.16 mono-
molecular layer of benzoate [0.25 nm2, roughness factor 3] was found on a steel
surface exposed 24 h to 0.1, 0.3, and 0.5% sodium benzoate solutions, respectively,
and inhibition was observed in all the solutions. Clearly, a very small amount of
benzoate on the metal surface increases adsorption of oxygen, or, alternatively,
decreases reduction of oxygen at cathodic areas. This effect is specific to the
cathodic areas of iron because iron continues to corrode in 0.5% sodium benzo-
ate when coupled to gold, on which the reduction of oxygen is apparently not
retarded.
The mechanism of inhibition in the case of sodium polyphosphate solutions
may depend in part on the ability of polyphosphates to interfere with oxygen
reduction on iron surfaces, making it easier for dissolved oxygen to adsorb and,
thereby, to induce passivity. Other factors enter as well; there is, for example,
evidence of protective film formation of the diffusion-barrier type on cathodic
PASSIVATORS 307
Figure 17.2. Effect of oxygen concentration on sodium polyphosphate as a corrosion inhibi-

tor of iron showing beneficial effect of dissolved O2 and Ca2+, 48-h test, 25°C [9]. (Reproduced
with permission. Copyright 1955, The Electrochemical Society.)
areas, and such diffusion-barrier films probably account for the observed inhibi-
tion of steel exposed to as high as 2.5% NaCl solutions containing several hundred
parts per million calcium polyphosphate [13]. At low concentration of dissolved
oxygen, corrosion of iron is accelerated by sodium polyphosphate because of its
metal-ion-complexing properties (Fig. 17.2). Calcium, iron, and zinc polyphos-
phates are better inhibitors than the sodium compound.
In line with the theory of passivators just described, transition metals are
those expected and found to be inhibited best by passivators; their anodic polar-
ization curves have the shape shown in Fig. 17.1, allowing passivity to be estab-
lished and then maintained at low current densities. A lesser degree of inhibition
can be obtained with the nontransition metals, such as Mg, Cu, Zn, and Pb, using,
for example, chromates. Protection of these metals apparently results largely
from formation of relatively thick diffusion-barrier films of insoluble metal
TABLE 17.1. Effect of Chromate Concentration, Chlorides, and Temperature on Corrosion

of Mild Steel [14]
Velocity of Specimen: 0.37 m/s; 14-day tests
Na2Cr2O7 · 2H2O (g/liter) → 0 0.1 0.5 1.0
% NaCl Temperature (°C) Corrosion Rate (mm/y)
0 20 0.539 0.002 0.002 0.001

75 0.905 0.356a 0.010 0.004
95 0.430 0.266a 0.011 0.000
0.002 20 0.668 0.015 0.001 0.001
75 1.705 0.120a 0.004 0.000
95 0.529 0.441a 0.131a 0.007
0.05 20 0.785 0.030 0.037 0.020
75 2.158 0.055 0.066 0.039
95 0.579 0.178a 0.120a 0.062
3.5 20 0.606 0.042 0.040 0.039
22.0 20 0.185 0.022 0.014 0.034
a
Pitted.
chromates mixed with oxides. There is also the possibility that adsorption of
CrO2−4 on the metal surface contributes in some degree to the lower reaction rate
by decreasing the exchange current density for the reaction M → M2+ + 2e−.
An inhibiting mechanism similar to that for nontransition metals in contact
with passivators probably also applies to steel in concentrated refrigerating brines
(NaCl or CaCl2) to which chromates are added as inhibitors (approximately
1.5–3.0 g Na2Cr2O7/liter adjusted with NaOH to form CrO2− 4 ). In the presence of
so large a Cl− concentration, passivity of the kind discussed under Definition 1
(Section 6.1) does not take place. The reduction in corrosion rate is not as pro-
nounced as when chlorides are absent [14] (see Table 17.1), and any reduction
that occurs apparently results from formation of a surface diffusion barrier of
chromate reduction products and iron oxides. Chromates are not adequate inhib-
itors for the hot concentrated brine solutions that, in the past, were sometimes
mistakenly proposed as antifreeze solutions for engine cooling systems.
17.2.2 Applications of Passivators

Chromates are applied mostly as inhibitors for recirculating cooling waters (e.g.,
of internal combustion engines, rectifiers, and cooling towers). The concentration
of Na2CrO4 used for this purpose is about 0.04–0.2%, with the higher concentra-
tions being employed at higher temperatures or in fresh waters of chloride con-
centration above 10 ppm. The pH is adjusted, if necessary, to 7.5–9.5 by addition
of NaOH. Periodic analysis (colorimetric) is required to ensure that the concen-
tration remains above the critical level (10−3 M or 0.016% Na2CrO4 at room
PASSIVATORS 309
temperature). Combinations of chromates with polyphosphates or other inhibi-

tors may permit the concentration of chromates to fall below the critical level.
This reduction in chromate concentration results in some sacrifice of inhibiting
efficiency, but there may be adequate protection against pitting for the treatment
of very large volumes of water employing cooling towers [15].
Chromates (Cr6+) are toxic and carcinogenic and cause a rash on prolonged
contact with the skin, and so they must be used with caution and with full regard
to disposal requirements.
Corrosion rates of mild steel as a function of chromate and chloride concen-
tration at various temperatures are shown in Table 17.1 [14].
Nitrites are used as inhibitors for antifreeze cooling waters (see Section
18.2.1) because, unlike chromates, they have little tendency to react with alcohols
or ethylene glycol. They are not so well-suited to cooling tower waters because
they are gradually decomposed by bacteria [16]. They are used to inhibit cutting
oil–water emulsions employed in the machining of metals (0.1–0.2%). In pipe-
lines transporting gasoline and other petroleum products, where water is a very
minor phase, sufficient nitrite or chromate solution may be continuously injected
to give a 2% concentration in the water phase [17]. In this connection, gasoline
is corrosive to steel because, on reaching lower temperatures underground, it
releases dissolved water which, in contact with large quantities of oxygen dis-
solved in the gasoline (solubility of O2 in gasoline is six times that in water), cor-
rodes steel, forming voluminous rust products that may clog the line. Sodium
nitrite enters the water phase and effectively inhibits rusting. Chromates used for
the same purpose have the disadvantage that they tend to react with some con-
stituents of the gasoline.
The corrosion rates of steel in contact with water–gasoline mixtures contain-
ing increasing amounts of NaNO2 are listed in Table 17.2 [18]. The minimum
amount of NaNO2 for effective inhibition is 0.06% or 7 × 10−3 M which, because
of impurities present in the water, is higher than the critical concentration in
distilled water. Nitrites are inhibitors only above about pH 6.0. In more acid
environments, they decompose, forming volatile nitric oxide and nitrogen
TABLE 17.2. Corrosion Rates of Mild Steel in Sodium

Nitrite Solutions Containing Gasoline [18]
Rotating Bottle Tests Using Pipeline Water, pH 9, and
Gasoline; 14-Day Exposure, Room Temperature
% NaNO2 Corrosion Rate (mm/y)
0.0 0.11
0.02 0.08
0.04 0.02
0.06 0.0
0.10 0.0
TABLE 17.3. Critical Concentrations of NaCl or Na2SO4 above

which Pitting of Armco Iron in Chromate or Nitrite Solutions
Occurs [11]a
5-Day Tests, 25°C, Stagnant Solutions
Critical Concentrations
NaCl Na2SO4
Na2CrO4 200 ppm 12 ppm 55 ppm

500 30 120
NaNO2 50 ppm 210 20
100 460 55
500 >2000 450
a
See also Refs. 4 and 5.
peroxide. In common with other passivators, they tend to induce pitting at con-
centrations near the critical in presence of Cl− or SO2− 4 ions. In this regard,
nitrates are less sensitive to Cl− than to SO2−
4 , contrary to the situation for chro-
mates [3–5] (Table 17.3).
17.3 PICKLING INHIBITORS
Most pickling inhibitors function by forming an adsorbed layer on the metal

surface, probably no more than a monolayer in thickness, which essentially
blocks discharge of H+ and dissolution of metal ions. For example, both iodide
and quinoline are reported to inhibit corrosion of iron in hydrochloric acid by
this mechanism [19]. Some inhibitors block the cathodic reaction (raise hydrogen
overpotential) more than the anodic reaction, or vice versa; but adsorption
appears to be general over all the surface rather than at specific anodic or
cathodic sites, and both reactions tend to be retarded. Hence, on addition of an
inhibitor to an acid, the corrosion potential of steel is not greatly altered (<0.1 V),
although the corrosion rate may be appreciably reduced (Fig. 17.3).
Compounds serving as pickling inhibitors require, by and large, a favorable
polar group or groups by which the molecule can attach itself to the metal
surface. These include the organic N, amine, S, and OH groups. The size, orienta-
tion, shape, and electric charge of the molecule play a part in the effectiveness
of inhibition. For example, the corrosion of iron in 1N hydrochloric acid was
found to be inhibited by derivatives of thioglycolic acid and 3-mercaptopropionic
acid to an extent that varied systematically with chain length [20]. Whether a
compound adsorbs on a given metal and the relative strength of the adsorbed
bond often depend on factors such as surface charge of the metal [21]. For inhibi-
tors that adsorb better at increasingly active potential as measured from the point
of zero surface charge (potential of minimum ionic adsorption), cathodic polar-
PICKLING INHIBITORS 311
Figure 17.3. Polarization diagram for steel corroding in pickling acid with and without
inhibitor.
ization in presence of the inhibitor provides better protection than either the
equivalent cathodic protection or use of an inhibitor alone. Antropov [22] dem-
onstrated this for iron and zinc in sulfuric acid containing various organic
inhibitors.
The anion of the pickling acid may also take part in the adsorbed film or
double-layer structure, accounting for differing efficiencies of inhibition for the
same compound in HCl compared to H2SO4. For example, the corrosion rate of
steel at 20°C inhibited with 20 g/liter quinoline is 26 gmd in 2N H2SO4, but only
4.8 gmd in 2N HCl, whereas the corrosion rates in the absence of inhibitor are
36 and 24 gmd, respectively [23]. In addition, specific electronic interaction of
polar groups with the metal (chemisorption) may account for a given compound
being a good inhibitor for iron, but not for zinc, or vice versa. The latter factor
in certain cases may be more important than the steric factor (diffusion-barrier
properties) of a closely packed, oriented layer of high-molecular-weight mole-
cules. This is shown by the outstanding inhibition provided by the simple mole-
cule carbon monoxide, CO, dissolved in HCl to which 18–8 stainless steel is
exposed [24]; in 6.3N HCl at 25°C, the inhibition efficiency is 99.8%, where the
inhibition efficiency is defined as
Percent inhibition efficiency = (rateno inhib − ratewith inhib) × 1000 /rateno inhib (17.1)
Very effective inhibition of corrosion of iron is also provided by a small amount

of iodide in dilute H2SO4 [25]. Both CO and iodide chemisorb on the metal
surface, interfering mostly with the anodic reaction [26]. Kaesche [27] showed
that 10−3 M KI is a much more effective inhibitor for iron in 0.5M Na2SO4 solution
at pH 1 (89% efficient) compared to pH 2.5 (17% efficient), indicating that
adsorption of iodide, particularly in this pH range, is pH-dependent.
The interaction of factors just mentioned, plus perhaps others, enter into
accounting for the fact that some compounds (e.g., o-tolylthiourea [28] in 5%
H2SO4) are better inhibitors at elevated temperatures than at room temperature,

presumably because adsorption increases or the film structure becomes more
favorable at higher temperatures. Others (e.g., quinoline derivatives) are more
efficient in the lower-temperature range [28].
Typical effective organic pickling inhibitors for steel are quinolinethiodide,
o- and p-tolylthiourea, propyl sulfide, diamyl amine, formaldehyde, and
p-thiocresol.
Inhibitors containing sulfur, although effective otherwise, sometimes induce
hydrogen embrittlement of steel in the event that the compound itself or hydro-
lysis products (e.g., H2S) are formed that favor entrance of H atoms into the
metal (see Section 5.5). In principle, inhibitors containing arsenic or phosphorus
can behave similarly.
17.3.1 Applications of Pickling Inhibitors

Pickling inhibitors used in practice are seldom pure compounds. They are usually
mixtures, which may be a byproduct, for example, of some industrial chemical
process for which the active constituent is unknown. They are added to a pickling
acid in small concentration, usually on the order of 0.01–0.1%. The typical effect
of concentration of an inhibitor on the reaction between steel and 5% H2SO4 is
illustrated [28] in Fig. 17.4, showing that, above a relatively low concentration,
presumably that necessary to form an adsorbed monolayer, an additional amount
of inhibitor has little effect on further reducing the rate.
Inhibitors are commonly used in the acid pickling of hot-rolled steel products
in order to remove mill scale. The advantages of using an inhibitor for this
purpose are (1) saving of steel, (2) saving of acid, and (3) reduction of acid fumes
Figure 17.4. Effect of inhibitor concentration on corrosion of 0.1% C steel in 5% H2SO4,

70°C [28].
VAPOR-PHASE INHIBITORS 313
caused by hydrogen evolution. Inhibited dilute sulfuric or hydrochloric acid is

also used to clean out steel water pipes clogged with rust, to clean boiler tubes
encrusted with CaCO3 or iron oxide scales, and to activate oil wells underground,
the inhibitor protecting steel oil-well tubing. For example, boiler scale can be
removed by using 0.1% hexamethylene tetramine in 10% HCl at a maximum
temperature of 70°C (160°F) [29].
17.4 SLUSHING COMPOUNDS
Slushing compounds are used to protect steel surfaces temporarily from rusting
during shipment or storage. They consist of oils, greases, or waxes containing
small amounts of organic additives. The latter are polar compounds that adsorb
on the metal surface in the form of a closely packed oriented layer. In this respect,
the mechanism of inhibition by organic additives is similar to that of inhibition
by pickling inhibitors, except that for use as slushing compounds, additives must
suitably adsorb in the near-neutral range of pH, whereas pickling inhibitors
adsorb best in the low pH range, calling for somewhat different properties.
Whether an oil or a wax is chosen as the vehicle depends on (1) the relative
length of time protection is desired, the wax usually providing longer life and (2)
the ease of removal before the protected machine part is put into service, with
an oil being easier to wipe off or dissolve in solvents. The thickness of an applied
coat varies from 0.1 mm to more than 2.5 mm (5 to more than 100 mils).
Suitable organic additives for use in slushing compounds include organic
amines, zinc naphthenate, various oxidation products of petroleum, alkali and
alkaline-earth metal salts of sulfonated oils, and various other compounds [30].
A substance that has been used successfully is lanolin, obtained from wool scour-
ing; its active constituents are various high-molecular-weight fatty alcohols and
acids. Sometimes, lead soaps are added to slushing compounds, with these soaps
reacting to form relatively insoluble PbCl2 with any NaCl from perspiration
transferred to steel surfaces through handling.
17.5 VAPOR-PHASE INHIBITORS
Substances of low but significant vapor pressure, the vapor of which has
corrosion-inhibiting properties, are called vapor-phase inhibitors. They are used
to protect critical machine parts (e.g., ball bearings or other manufactured steel
articles) temporarily against rusting by moisture during shipping or storage. They
have the advantage over slushing compounds of easy application, with the pos-
sibility of immediate use of the protected article without first removing a residual
oil or grease film. They have the disadvantgage of accelerating the corrosion of
some nonferrous metals, discoloring some plastics, and requiring relatively effec-
tive sealing of a package against loss of the inhibiting vapor. The latter require-
ment is relatively easily achieved, however, by using wrapping paper impregnated
on the inside surface with the inhibitor and incorporating a vapor-barrier coating
on the outside.
The mechanism of inhibition has not been studied in detail, but it appears
to be one of adsorbed film formation on the metal surface that provides protec-
tion against water or oxygen, or both. In the case of volatile nitrites, the inhibitor
may also supply a certain amount of NO−2 that passivates the surface.
Detailed data have been presented for dicyclohexylammonium nitrite [31],
which is one of the most effective of the vapor-phase inhibitors. This substance
is white, crystalline, almost odorless, and relatively nontoxic. It has a vapor pres-
sure of 0.0001 mmHg at 21°C (70°F), which is about one-tenth the vapor pressure
of mercury itself.* One gram saturates about 550 m3 (20,000 ft3) of air, rendering
the air relatively noncorrosive to steel. The compound decomposes slowly;
nevertheless, in properly packaged paper containers at room temperature, it
effectively inhibits corrosion of steel over a period of years. However, it should
be used with caution in contact with nonferrous metals. In particular, corrosion
of zinc, magnesium, and cadmium is accelerated.
Cyclohexylamine carbonate has the somewhat higher vapor pressure of
0.4 mmHg at 25°C and its vapor also effectively inhibits steel [32]. The higher
vapor pressure provides more rapid inhibition of steel surfaces either during
packaging or on opening and again on closing a package, during which time the
concentration of vapor may fall below that required for protection. The vapor
is stated to reduce corrosion of aluminum, solder, and zinc, but it has no inhibit-
ing effect on cadmium, and it increases corrosion of copper, brass, and
magnesium.
Ethanolamine carbonate and various other compounds have also been
described as vapor-phase inhibitors [23, 32]. A combination of urea and sodium
nitrite has found practical application, including use in impregnated paper. The
mixture probably reacts in the presence of moisture to form ammonium nitrite,
which is volatile, although unstable, and conveys inhibiting nitrite ions to the
metal surface.
17.5.1 Inhibitor to Reduce Tarnishing of Copper

Benzotriazole (BTA), C6H5N3, is a corrosion inhibitor widely used for copper and
its alloys. Typical protective films formed on copper are reported to consist of
various multilayers. Film thickness is normally controlled by the pH of the solu-
tion, ranging from less than 0.01 μm in near-neutral and mildly basic solutions to
0.5 μm in acidic solutions [33]. For a wide variety of conditions [34], this inhibitor
is reported to form a Cu+ surface complex following its adsorption on Cu2O that
is present on copper surfaces.
*I. Rosenfeld et al. (Symposium sur les Inhibiteurs de Corrosion, University of Ferrara, Italy, 1961,
p. 344) report the lower value of 0.00001 mmHg obtained for dicyclohexylammonium nitrite carefully
purified by multiple recrystallization from alcohol.
REFERENCES 315
REFERENCES
1. H. Uhlig and P. King, J. Electrochem. Soc. 106, 1 (1959).

2. W. Robertson, J. Electrochem. Soc. 98, 94 (1951).
3. S. Matsuda and H. Uhlig, J. Electrochem. Soc. 111, 156 (1964).
4. A. Mercer and I. Jenkins, Br. Corros. J. 3, 130 (1968).
5. A. Mercer, I. Jenkins, and J. Rhoades-Brown, Br. Corros. J. 3, 136 (1968).
6. M. Pryor and M. Cohen, J. Electrochem. Soc. 100, 203 (1953).
7. D. Brasher and A. Mercer, Br. Corros. J. 3, 120 (1968).
8. F. Wormwell, Chem. Ind. (London) 1953, 556.
9. H. Uhlig, D. Triadis, and M. Stern, J. Electrochem. Soc. 102, 59 (1955).
10. G. Hatch, Mater. Prot. 8, 31 (1969).
11. S. Matsuda, D. Sc. thesis, Department of Metallurgy, M.I.T., Cambridge, MA, 1960.
12. H. Gatos, in Symposium sur les Inhibiteurs de Corrosion, University of Ferrara, Italy,
1961, p. 257.
13. G. Butler and D. Owen, Corros. Sci. 9, 603 (1969).
14. B. Roetheli and G. Cox, Ind. Eng. Chem. 23, 1084 (1931).
15. H. Kahler and P. Gaughan, Ind. Eng. Chem. 44, 1770 (1952).
16. T. P. Hoar, Corrosion 14, 103t (1958).
17. J. Bregman, Inhibition in the petroleum industry, in Proceedings of the Third European
Symposium on Corrosion Inhibitors, University of Ferrara, Italy, 1970, p. 365.
18. A. Wachter and S. Smith, Ind. Eng. Chem. 35, 358 (1943).
19. K. Rajagopalan and G. Venkatachari, Corrosion 36, 320 (1980).
20. M. Carroll, K. Travis, and J. Noggle, Corrosion 31, 123 (1975).
21. L. Antropov, Kinetics of Electrode Processes and Null Points of Metals, Council of Sci-
entific & Industrial Research, New Delhi, 1960, pp. 48–82.
22. L. Antropov, Inhibitors of metallic corrosion and the phi-scale of potentials, First
International Congress on Metallic Corrosion, Butterworths, London, 1961, p. 147.
23. I. Putilova, S. Balezin, and V. Barannik, Metallic Corrosion Inhibitors, G. Ryback,
translator, Pergamon Press, New York, 1960, p. 63.
24. H. Uhlig, Ind. Eng. Chem. 32, 1490 (1940).
25. K. Hager and M. Rosenthal, Ordnance 35, 479 (1951).
26. K. Heusler and G. Cartledge, J. Electrochem. Soc. 108, 732 (1961).
27. H. Kaesche, in Symposium sur les Inhibiteurs de Corrosion, University of Ferrara,
Italy, 1961, p. 137.
28. T. Hoar and R. Holliday, J. Appl. Chem. 3, 502 (1953).
29. W. Cerna, Proceedings of the Seventh Annual Water Conference, Pittsburgh, PA,
1947.
30. H. Baker and W. Zisman, Ind. Eng. Chem. 40, 2338 (1948).
31. A. Wachter, T. Skei, and N. Stillman, Corrosion 7, 284 (1951).
32. E. Stroud and W. Vernon, J. Appl. Chem. 2, 178 (1952).
33. I. Ogle and G. Poling, Can. Metall. Q. 14, 37 (1975).
34. D. Chadwick and T. Hashemi, Corros. Sci. 18, 39 (1978).
GENERAL REFERENCES
B. P. Boffardi, Corrosion inhibitors in the water treatment industry, in ASM Handbook,

Vol. 13A, Corrosion: Fundamentals, Testing, and Protection, ASM International, Materi-
als Park, OH, 2003, pp. 891–906.
R. L. Martin, Corrosion inhibitors for oil and gas production, in ASM Handbook, Vol. 13A,
OH, 2003, pp. 878–886.
S. Papavinasam, Corrosion inhibitors, in Uhlig’s Corrosion Handbook, 2nd edition, R. W.
S. Papavinasam, Evaluation and selection of corrosion inhibitors, in Uhlig’s Corrosion
Handbook, 2nd edition, R. W. Revie, editor, Wiley, New York, 2000, pp. 1169–1178.
J. D. Poindexter, Corrosion inhibitors for crude oil refineries, in ASM Handbook, Vol. 13A,
OH, 2003, pp. 887–890.
V. S. Sastri, Corrosion Inhibitors: Principles and Applications, Wiley, Chichester, 1998.
K. L. Vasanth, Vapor phase corrosion inhibitors, in ASM Handbook, Vol. 13A, Corrosion:
Fundamentals, Testing, and Protection, ASM International, Materials Park, OH, 2003,
pp. 871–877.
18
TREATMENT OF WATER
AND STEAM SYSTEMS
18.1 DEAERATION AND DEACTIVATION
In accord with principles described in Sections 7.1 and 7.2, corrosion of iron is
negligible at ordinary temperatures in water that is free of dissolved oxygen. An
effective practical means, consequently, for reducing corrosion of iron or steel in
contact with fresh water or seawater is to reduce the dissolved oxygen content.
In this way, corrosion of copper, brass, zinc, and lead is also minimized.
Removal of dissolved oxygen from water is accomplished either by chemi-
cally reacting oxygen beforehand, called deactivation, or by distilling it off in
suitable equipment, called deaeration. Deactivation can be carried out in practice
by slowly flowing hot water over a large surface of steel laths or sheet contained
in a closed tank called a deactivator. The water remains in contact long enough
to corrode the steel, and, by this process, most of the dissolved oxygen is con-
sumed. Subsequent filtration removes suspended rust. Water so treated is much
less corrosive to a metal pipe distribution system. Deactivators of this kind have
been employed in some buildings, but, since use of deactivation requires regular
attention in addition to periodic renewal of the steel sheet, this approach to

317
318 TREATMENT OF WATER AND STEAM SYSTEMS
oxygen removal is usually too cumbersome compared with the use of chemical
inhibitors or deaeration.
Deactivation of industrial waters (not potable waters, because the chemicals
used are toxic) is possible by using oxygen scavengers (strong reducing agents),
such as sodium sulfite (Na2SO3) and hydrazine (N2H2), which function as corro-
sion inhibitors by removing the oxygen. Since hydrazine has been identified as a
possible carcinogen, there have been considerable efforts to replace it.
Sodium sulfite scavenges oxygen in accord with the reaction
1
Na 2 SO2 + O2 → Na 2 SO4 (18.1)
2
for which Na2SO3 reacts with oxygen in the weight ratio of 8 : 1 (8 kg Na2SO3 to
1 kg O2). The reaction is relatively fast at elevated temperatures, but slow at
ordinary temperatures. It can be accelerated by adding catalysts, such as Cu2+ or
Co2+, salts [1, 2].
The rapid decrease with time of dissolved oxygen in the San Joaquim, Cali-
fornia, river water after treatment with 80 ppm Na2SO3 (0.67 lb/1000 gal) plus
copper or cobalt salts is shown in Fig. 18.1. Water so treated using CoCl2 as cata-
lyst was found by Pye [1] to be noncorrosive to a steel heat-exchanger system
that, without treatment, had previously suffered serious corrosion and loss of
heat transfer. Tests showed a reduction in corrosion rate from 0.2 mm/y (0.008 ipy,
pitting factor = 7.4) before treatment to 0.004 mm/y (0.00016 ipy) afterward.
Hydrazine (N2H4), supplied as a concentrated aqueous solution, also reacts
with dissolved oxygen, according to
Figure 18.1. Effect of cobalt and copper salts on reaction rate of Na2SO3 with dissolved
oxygen at room temperature [1]. [Reprinted from Journal AWWA 39 (11) (November 1947),
by permission. Copyright 1947, American Water Works Association.]
DEAER ATION AND DEAC TIVATION 319
N 2 H 4 + O2 → N 2 + 2 H 2O (18.2)
in the weight ratio of 1 : 1. This reaction is slow at ordinary temperatures, but can
be accelerated by using catalysts (e.g., activated charcoal, metal oxides, alkaline
solutions [3] of Cu2+ and Mn2+) and by raising the temperature. At elevated
temperatures, decomposition occurs slowly at 175 °C (345 °F) and more rapidly
at 300 °C (570 °F), producing ammonia [4]:
3N 2 H 4 → N 2 + 4 NH 3 (18.3)
The normal reaction products—nitrogen, water, and a small amount of NH3—are

all volatile, and, unlike sulfite addition, no dissolved solids accumulate in the
treated water.
Two additional oxygen scavengers are carbohydrazide, (NH2NH)2CO,
and diethylhydroxylamine (DEHA), (C2H5)2NOH; the reactions with oxygen
are
(NH 2 NH)2 CO + 2O2 → 2 N 2 + 3H 2O + CO2 (18.4)
and
4(C 2 H 5)2 NOH + 9O2 → 8CH 3COOH + 2 N 2 + 6H 2O (18.5)
Both these oxygen scavengers have the additional advantage that they form
protective films on both iron and copper [5].
Deaeration is accomplished by spraying water or flowing it over a large
surface, countercurrent to steam. Oxygen distills off and also some dissolved
carbon dioxide (Fig. 18.2). Water is heated in the process and is suitable, there-
fore, as feedwater for boilers. Steam deaerators of this kind are standard equip-
ment for all high-pressure stationary boilers. On the other hand, if the water is
to be used cold, dissolved gases are distilled off by lowering the pressure, employ-
ing a mechanical pump or steam ejector instead of a countercurrent flow of
steam. This is called vacuum deaeration. Equipment of this kind has been
designed to deaerate several million gallons of water per day.
In principle, it is more difficult and more expensive to remove the last traces
of dissolved oxygen by distillation compared to the first 90–95%, and it is more
difficult at low temperatures than at high temperatures. To achieve a low enough
oxygen level in cold water, it is often necessary to use multiple-stage vacuum
treatment. Fortunately, acceptable levels of dissolved oxygen for corrosion
control in cold water are higher than in hot water or in steam. Allowable levels
established through experience are given in Table 18.1 [6].
Figure 18.2. Sketch of one type of steam deaerator.
TABLE 18.1. Approximate Allowable Oxygen Concentration in Deaerated Water for

Corrosion Control in Steel Systems
Maximum Oxygen
Concentration
ppm mL/liter
Cold water 0.3 0.2

Hot water 0.1 0.07
Low-pressure boilers (<1.7 MPa, <250 psi) 0.03 0.02
High-pressure boilers 0.005 0.0035
HOT- AND COLD-WATER TREATMENT 321
18.2 HOT- AND COLD-WATER TREATMENT
1. Hot-Water Heating Systems. These are closed steel systems in which the
initial corrosion of the system soon consumes dissolved oxygen; corrosion
is negligible once the dissolved oxygen is consumed. A continuing minor
reaction of steel with water produces hydrogen, with a characteristic odor
due to traces of hydrocarbon gases originating from the reaction of car-
bides in steel with water. The hydrogen reaction can be minimized by
treating the water with NaOH or Na3PO4 to a pH of 8.5.
2. Municipal Water Supplies. Usually, hard waters of positive saturation
index are relatively noncorrosive and do not require treatment of any kind
for corrosion control. Soft waters, on the other hand, cause rapid accu-
mulation of rust in ferrous piping, are readily contaminated with toxic
quantities of lead salts on passing through lead piping, and cause blue
staining of bathroom fixtures by copper salts originating from slight cor-
rosion of copper or brass piping.
Chemical treatment of potable waters is limited to small concentrations of

inexpensive, nontoxic chemicals, such as polyphosphates, orthophosphates, and
silicates. Zinc polyphosphate has been used for more than 60 years in controlling
corrosion of steel in municipal water systems. Zinc orthophosphate is effective
in controlling corrosion of steel, copper, and lead.
Raising the saturation index is a potentially useful means for reducing the
corrosion rate in either flowing or stagnant portions of the distribution system,
and it is also effective for reducing corrosion of hot-water systems. This treatment
requires addition of lime [Ca(OH)2] or both lime and soda ash (Na2CO3) to the
water in amounts that raise the saturation index to about +0.5 (see Section
7.2.6.1). For the treatment to be successful, the water must be low in colloidal
matter and in dissolved solids other than calcium salts. Corrosion of copper, lead,
and brass is also reduced by this treatment. In hot-water systems, the possibility
of excess deposition of CaCO3, which causes scaling, must be taken into account
in arriving at the proper proportions of added chemicals.
Sodium silicate treatment in the amount of about 4–15 ppm SiO2 is sometimes
used by individual owners of buildings in soft-water areas. This treatment reduces
“red water” caused by suspended rust resulting from corrosion of ferrous piping,
and it also eliminates blue staining by water that has passed through copper or
brass piping.
The conditions under which protection exists or is optimum are not entirely
understood, but it is clear that dissolved calcium and magnesium salts have an
effect and that some protection may result alone from the alkaline properties of
sodium silicate. In the presence of silicate, passivity of iron may be observed at
pH 10 with an accompanying reduction of the corrosion rate to 0.1–0.7 gmd [7].
Sodium hydroxide induces similar passivity and corresponding low corrosion
rates at the somewhat higher pH range of 10–11. Under other conditions (e.g.,
pH 8), a protective diffusion-barrier film is formed, apparently containing SiO2
and consisting perhaps of an insoluble iron silicate. Laboratory tests in distilled

water at 25 °C showed a reduction in the corrosion rate of iron on the order of
85–90% when sodium silicate was added to bring the pH to 8 [7]. However, no
inhibition was obtained in the laboratory at the same SiO2 content using Cam-
bridge tap water (pH 8.3, 44 ppm Ca, 10 ppm Mg, 16 ppm Cl−). If larger quantitites
of sodium silicate were added to raise the pH of the water to 10 or 11, the range
in which passivity of iron occurs, a marked decrease in the corrosion rate was
observed.
Domestic or industrial hot-water heaters of galvanized steel through which
hot aerated water passes continuously are not protected reliably in all types of
water by nontoxic chemical additions such as silicates or polyphosphates. Adjust-
ment of the saturation index to a more positive value, as discussed earlier, is
sometimes helpful. Often, cathodic protection or use of nonferrous metals, such
as copper or 70% Ni–Cu (Monel), is the best or only practical measure.
18.2.1 Cooling Waters

Once-through cooling waters (usually obtained from rivers, lakes, or wells)
usually cannot be treated chemically, both because of the large quantities of
inhibitors required and because of the problem of water pollution. Sometimes,
additions of about 2–5 ppm sodium or calcium polyphosphate are made to help
reduce corrosion of steel equipment. In such small concentrations, polyphos-
phates are not toxic, but water disposal may continue to be a problem because
of the need to avoid accumulation of phosphates in rivers and lakes. Adjustment
of the saturation index to a more positive value is sometimes a practical possibil-
ity. Otherwise, a protective coating or metals more corrosion resistant than steel
must be used.
Recirculating cooling waters, as for engine-cooling systems, may be treated
with sodium chromate (Na2CrO4) in the amount of 0.04–0.2% (or the equivalent
amount of Na2Cr2O7·2H2O plus alkali to pH 8). Chromates inhibit corrosion of
steel, copper, brass, aluminum, and soldered components of such systems. Since
chromate is consumed slowly, additions must be made periodically in order to
maintain the concentration above the critical. For diesel or other heavy-duty
engines, 2000 ppm sodium chromate (0.2%) can be used to reduce damage by
cavitation-erosion as well as by aqueous corrosion (see Section 7.2.5.1). Because
of the toxicity of hexavalent chromium (Cr+6), chromates must be handled, used,
and disposed of appropriately and with regard to regulatory requirements.
Chromates cannot be used in the presence of antifreeze solutions, because
of their tendency to react with organic substances. Many proprietary inhibitor
mixtures are on the market that are usually dissolved beforehand in methanol
or in ethylene glycol in order to simplify the packaging problem, but this also
limits the available number of suitable inhibitors. In the United States, borax
(Na2B4O7·10H2O) is a common ingredient. Sulfonated oils, which produce an
oily protective coating, and mercaptobenzothiazole, which specifically inhibits
corrosion of copper and at the same time removes the accelerating influence of
BOILER-WATER TREATMENT 323
dissolved Cu2+ on corrosion of other portions of the system, are sometimes

added to borax. One specification calls for a final concentration in the antifreeze
solution of 1.7% borax, 0.1% mercaptobenzothiazole, and 0.06% Na2HPO4, with
the latter being added specifically to protect aluminum. Ethanolamine phos-
phate is also used as an inhibitor for engine-cooling systems containing ethylene
glycol.
For industrial water cooled by recirculation through a spray or tray-type
tower, chromates are the most reliable from the standpoint of efficient inhibition.
However, the critical concentration is high; and as the sulfate and chloride con-
centrations increase through evaporation of the water, chromates tend to cause
pitting or may cause increased galvanic effects at dissimilar metal couples.
Windage losses (loss of spray by wind) must be carefully avoided because chro-
mates are toxic. Toxicity also makes it difficult to dispose of chromate solutions
whenever it becomes necessary to reduce the concentration of accumulated
chlorides and sulfates.
Because of pollution problems that can be caused by chromates, numerous
inhibitor systems have been developed as alternatives—for example, organic
phosphonic acids, which are effective in alkaline waters and are biodegradable
[8]. Nontoxic inhibitor formulations containing mixtures of azoles and water-
soluble phosphates (e.g., disodium phosphate and sodium tripolyphosphate)
have been developed [9]. Sodium molybdate, which is less toxic than sodium
chromate, has also been reported to be a useful component of inhibitor formula-
tions for use in recirculating aqueous systems [9, 10]. Other nontoxic, chromate-
free inhibitor formulations are based on mixtures of sorbitol, benzotriazole or
tolytriazole, and water-soluble phosphates [9].
Sodium polyphosphate is often used in a concentration of about 10–100 ppm,
sometimes with added zinc salts to improve inhibition. The pH value is adjusted
to 5–6 in order to minimize pitting and tubercle formation, as well as scale depo-
sition. Polyphosphates decompose slowly into orthophosphates, which, in the
presence of calcium or magnesium ions, precipitate insoluble calcium or magne-
sium orthophosphate, causing scale formation on the warmer parts of the system.
Unlike chromates, they favor algae growth, which necessitates the addition of
algaecides to the water. Corrosion inhibition with polyphosphates is less effective
than that by chromates, but polyphosphates in low concentration are not toxic,
and the required optimum amount of inhibitor is less than that for chromates.
18.3 BOILER-WATER TREATMENT
18.3.1 Boiler Corrosion

Steam boilers are constructed according to various designs, but they consist
essentially of a low-carbon steel or low-alloy steel container for water that is
heated by hot gases. The steam may afterward pass to a superheater of higher-
alloy steel at higher temperature than the boiler itself. For maximum heat
transfer, a series of boiler tubes is usually used, with the hot gases passing either
around the outer surface or, less frequently, through the inner surface of the
tubes. The steam, after doing work or completing some other kind of service,
eventually reaches a condenser that is usually constructed of copper-base alloy
tubes. Steam is cooled on one side of the tubes by water passing along the oppo-
site side of a quality ranging from fresh to polluted, brackish, or seawater. The
condensed steam then returns to the boiler and the cycle repeats.
The history and causes of corrosion in power-station boilers have been
reviewed by Mann [11]; case histories of corrosion and its prevention in industrial
boilers have been presented by Frey [12].
Some boilers are equipped with an embrittlement detector by means of
which the chemical treatment of a water can be evaluated continuously in terms
of its potential ability to induce stress-corrosion cracking (Fig. 18.3) [13]. A speci-
men of plastically deformed boiler steel is stressed by setting a screw; adjustment
of this screw regulates a slight leak of hot boiler water in the region where the
specimen is subject to maximum tensile stress and where boiler water evaporates.
A boiler water is considered to have no embrittling tendency if specimens do not
crack within successive 30-, 60-, and 90-day tests. Observation of the detector is
Figure 18.3. Embrittlement detector which, when attached to an operating boiler, detects
tendency of a boiler water to induce stress-corrosion cracking.
a worthwhile safety measure because the tendency toward cracking is more pro-
nounced in the plastically deformed test piece than in any portion of the welded
boiler; hence, water treatment can be corrected, if necessary, before the boiler
is damaged.
Corrosion of boiler and superheater tubes is sometimes a problem on the
hot combustion gas side, especially if vanadium-containing oils are used as fuel.
This matter is discussed in Sections 11.8 and 11.9. On the steam side, since
modern boiler practice ensures removal of dissolved oxygen from the feedwater,
a reaction occurs between H2O and Fe, resulting in a protective film of magnetite
(Fe3O4) as follows:
3Fe + 4 H 2O → Fe3O4 + 4 H 2 (18.6)
The mechanism of this reaction, so far as it is understood, indicates that Fe3O4

is formed only below about 570 °C (1060 °F) and that above this temperature,
FeO forms instead. The latter then decomposes on cooling to a mixture of mag-
netite and iron in accord with
4 FeO → Fe3O4 + Fe (18.7)
Measurements of hydrogen accumulation in boilers as a function of time, as well

as laboratory corrosion rate determinations, indicate that growth of the oxide
obeys the parabolic equation [14]. Hence, the rate is diffusion-controlled, in line
with the mechanism depending on ion and electron migration through solid reac-
tion products as described in Chapter 11.
At lower temperatures (e.g., room temperature to about 100 °C) and proba-
bly at higher temperatures before a relatively thick surface film develops, experi-
ments show that Fe(OH)2 is the initial reaction product and not Fe3O4 [15]. The
mechanism of corrosion in this temperature range follows that described for
anode and cathode interaction on the plane of the metal surface in contact with
an electrolyte. Ferrous hydroxide eventually decomposes, at a rate depending on
temperature, into magnetite and hydrogen in accord with a reaction first described
by Schikorr (Schikorr reaction)[16]
3Fe(OH)2 → Fe3O4 + H 2 + 2 H 2O (18.8)
Any factors that disturb the protective magnetite layer on steel, either chem-
ically or mechanically, induce a higher rate of reaction, usually in a localized
region, causing pitting or sometimes grooving of the boiler tubes. In this regard,
the specific damaging chemical factor of excess OH− concentration is discussed
later; mechanical damage, on the other hand, may take place each time the
boiler is cooled down. Differential contraction of the oxide and metal causes
some degree of spalling of the oxide, thereby exposing fresh metal. Accordingly,
it is observed that rate of hydrogen evolution is momentarily high after a boiler
is started up again, with hydrogen production then falling to normal values
presumably after a reasonable thickness of oxide has again built up at damaged

areas.
Conditions of boiler operation that lead to metal oxide or inorganic deposits
(from the boiler itself or from condenser leakage) on the water side of boiler
tubes cause local overheating accompanied by additional precipitation of solutes
from the water. Pitting usually results, or so-called plug-type oxidation occurs,
which accentuates local temperature rise, leading eventually to stress rupture of
the tube. Furthermore, hydrogen resulting from the H2O–Fe corrosion reaction
may enter the steel causing decarburization, followed by microfissuring along
grain boundaries and eventual blowout of the affected tube. The latter type of
failure may take place without any major loss of tube wall thickness. In the
absence of deposits within boiler tubes, these types of damage are not observed
[17].
18.3.2 Boiler-Water Treatment for Corrosion Control

Feedwaters of boilers are chemically treated both to reduce corrosion of the
boiler and auxiliary equipment and to reduce formation of inorganic deposits on
the boiler tubes (scaling), which interfere with heat transfer. If steam is used for
power production, concentrations of silica and silicates in feedwaters must also
be reduced in order to minimize volatilization of SiO2 with steam, causing forma-
tion of damaging deposits on turbine blades. Control of scale formation usually
requires removing all calcium and magnesium salts by various means, including
use of ion-exchange resins or adding substances to the water that favor precipita-
tion of sludges rather than adherent continuous scales on the metal surface.
Details are discussed in standard references on boiler-water treatment.
For corrosion control, the basic treatment consists of removal of dissolved
gases, addition of alkali, and addition of inhibitors, as described in the following
paragraphs.
1. Removal of Dissolved Oxygen and Carbon Dioxide. For high-pressure

boilers, any remaining dissolved oxygen in the feedwater combines quantitatively
with the metals of the boiler system, usually causing pitting of the boiler tubes
and general attack elsewhere. Removal of oxygen is accomplished by steam
deaeration of the water, followed by addition of a scavenger, such as sodium
sulfite or hydrazine (see Section 18.1). Final oxygen concentration is usually held
below values (<0.005 ppm O2) analyzable by chemical methods (e.g., the Winkler
method).
Deaeration is accompanied by some reduction of carbon dioxide content,
particularly if the water is acidified before the deaeration process to liberate
carbonic acid from the dissolved carbonates. Carbonic acid is corrosive to steel
in the absence of dissolved oxygen and more so in its presence [18], but addition
of alkali to boiler water limits any corrosion caused by carbon dioxide to the
boiler itself by converting dissolved carbon dioxide to carbonates. At prevailing
boiler temperatures, however, carbonates dissociate as follows:
Na 2CO3 + H 2O → CO2 + 2NaOH (18.9)
bringing hot carbonic acid into contact with the condenser and return-line
systems. Steel return-line systems suffer serious corrosion, therefore, if the carbon
dioxide content of boiler water is high. Soluble FeCO3 is formed, and it returns
with the condensate to the boiler, where it decomposes into Fe(OH)2 + CO2, with
the carbon dioxide again being available for further corrosion. The copper-alloy
condenser system also suffers corrosion should dissolved oxygen be present
together with carbon dioxide, but attack of copper-base alloys is negligible in the
absence of oxygen. Since carbon dioxide is not used up in the corrosion process,
it accumulates increasingly in the boiler with each addition of feedwater unless
an occasional blowdown (intentional release of some boiler water) is arranged.
2. Addition of Alkali. Alkali addition to boiler waters is standard practice

for most high-pressure boilers in the United States and abroad. Feedwater for a
high-pressure boiler is treated to a minimum pH (measured at room tempera-
ture) of 8.5 to minimize corrosion of steel, with the optimal pH range being 9.2–
9.5. For copper alloys, the preferred pH range is 8.5–9.2. Since both steel and
copper alloys are common in boiler systems, a compromise range of 8.8–9.2 is
recommended [19].
It is apparent from Figure 18.4 that excess alkali can be damaging to a boiler
in that the corrosion rate increases rapidly as pH is increased above 13. The
Figure 18.4. Corrosion of iron by water at 310 °C (590 °F) at various values of pH measured
at 25 °C [E. Partridge and R. Hall, Trans. Am. Soc. Mech. Eng. 61, 597 (1939)].
Figure 18.5. Structural formulas for three neutralizing-type amines.
danger is not so much that the initial pH of the boiler water may be too high as
that accidental concentration of an alkaline boiler water at a crevice, such as is
formed between riveted plates, at a weld, beneath a cracked oxide scale, or at a
hot spot on a scaled tube surface, may reach OH− concentration levels above the
safe range. For this reason, it is held advisable to add buffer ions, such as PO3−
4
(Na3PO4), which limit the increase in pH that a water can achieve no matter how
concentrated it becomes. Such ions are also useful in avoiding similar high OH−
concentrations that lead to stress-corrosion cracking of any portion of the boiler
under high residual or applied stress. Goldstein and Burton [17] reported that
5–10 ppm phosphate at pH 9.5–10.0 was more effective in reducing corrosion of
high-pressure boiler tubes under a variety of operating conditions than either
NaOH or NH3 treatment.
3. Addition of Inhibitors. It is possible to add inhibitors for controlling two

kinds of corrosion in boiler systems, namely, stress-corrosion cracking and return-
line corrosion. The first can be minimized by addition of phosphates, as men-
tioned previously.
Corrosion caused by dissolved carbon dioxide in steam condensate is mini-
mized by adding a volatile amine to the boiler water. There are two categories
of volatile amines used for this purpose: (1) neutralizing amines and (2) filming
amines. The first group includes cyclohexylamine, benzylamine, and morpholine
(Fig. 18.5). When any of these is added to boiler water in sufficient amount, it
neutralizes carbonic acid and raises the pH of steam condensate to an alkaline
value, thereby making the condensate less corrosive. Operating by a different
principle, volatile octadecylamine, hexadecylamine, and dioctadecylamine are
typical of the filming-type inhibitors, which protect against corrosion by building
up a protective organic film on the condenser surface. The filming amines more
nearly fit the definition of an inhibitor, whereas the other amines are actually,
for the most part, neutralizers.
18.3.3 Mechanisms
Considerable progress has been made in elucidating the mechanisms and causes
of boiler corrosion. Advances in this area have been assisted by the development
of experimental techniques for studies at high temperature and high pressure

[20]. Potential–pH, or Pourbaix, diagrams have been developed for some systems
at elevated temperature, so that equilibria under specific potential and pH condi-
tions may be more readily predicted [21].
In high-temperature aqueous environments, iron and iron alloys form a
characteristic double oxide layer [22], with the layers in deoxygenated solutions
consisting of magnetite, Fe3O4. The outer layer consists of loosely packed crystals
>1 μm in diameter, whereas the inner protective layer consists of densely packed
crystallites 0.05–0.2 μm in diameter that adhere tightly to the underlying metal.
In solutions of too high or too low pH, however, the protective layer of magnetite
dissolves or is undermined, accounting for higher corrosion rates. The effects of
dissolved O2 are more complex.
Removal of dissolved oxygen is generally agreed upon as a necessary step in
all boiler-water treatment. Oxygen is damaging primarily because it initiates
pitting, possibly through action of differential aeration cells. The limiting safe
concentration of dissolved O2 is reported to depend inversely on the Cl− concen-
tration in the boiler water. In other words, dissolved neutral chlorides are not a
corrosion problem in the absence of dissolved O2, and the presence of dissolved
O2 is not a problem in sufficiently pure water [11].
Traces of O2, even if not damaging to the steel boiler directly, are neverthe-
less effective in causing attack of the condenser system, especially if CO2 or NH3
is also present in the condensate. Such corrosion is sufficient to return small
amounts of copper salts to the boiler followed by deposition of metallic copper.
Although the condensers may not be damaged appreciably by such corrosion,
the question remains whether pitting of the boiler is initiated by copper contami-
nation of boiler waters.
Whether a particular boiler is damaged by a given water treatment is not
evidence in itself that the treatment, in general, is good or bad. Statistical analysis
of many boilers, or a fundamental investigation of corrosion mechanisms, is
required in order to obtain a final answer. There are many interacting factors—
including feedwater composition, condenser leakage, boiler design, and boiler
operation, varying from one boiler to another—that determine whether oxygen
and copper contamination in specific instances are damaging.
Alkali Additions. The optimum alkalinity of a boiler water depends, in part,

on the extent to which contaminants slowly leak into the boiler from the cooling
water of the condenser system (usually at the interface of condenser tubes and
tubesheet). Leakage will vary with design and age of the condenser system;
ensuing effects on the boiler depend on the composition of a specific cooling
water. If, for example, seawater is used for cooling, magnesium chloride, which
is a natural constituent of seawater, hydrolyzes to HCl and causes acid attack of
the boiler. Periodic sodium hydroxide additions to the boiler water neutralize
the acid and prevent such attack [23]. In this regard, NH4OH is less effective than
NaOH + Na3PO4 as a neutralizing agent in the quantities of each usually used in
boiler-water treatment.
Excess alkali, on the other hand, is damaging because it may slowly dissolve
the magnetite film in accord with
Fe3O4 + 4 NaOH → 2 NaFeO2 + Na 2 FeO2 + 2 H 2O (18.10)
forming sodium hypoferrite or sodium ferroate (Na2FeO2) and sodium ferrite

(NaFeO2), both of which are soluble in hot concentrated NaOH. In addition,
concentrated alkali reacts directly and more rapidly with iron to form hydrogen
and sodium ferroate
Fe + 2 NaOH → Na 2 FeO2 + H 2 (18.11)
Reactions of this kind account in part for pitting and grooving of boiler tubes
and are those that account for the excessive corrosion rate of iron at high values
of pH, as Fig. 18.4 shows. As mentioned earlier, corrosive concentrations of
NaOH are usually built up by evaporation of alkaline boiler water at various
crevices where liquid flow is impeded and heat transfer is restricted. In the
absence of conditions that favor concentration of alkaline solutes, damage by
corrosion is expected to be minimal. Furthermore, phosphate additions avoid the
high values of pH in concentrated boiler water that are necessary for reactions
(18.10) and (18.11).
Oxygen Scavengers. The use of sodium sulfite as a scavenger in high-

pressure boilers is limited by the decomposition of sulfites at high temperatures
into sulfides or SO2. It is said to be satisfactory below 12.4 MPa (1800 psi) steam
pressure. One possible path for decomposition is the following:
4 Na 2SO3 + 2 H 2O → 3Na 2SO4 + 2 NaOH + H 2S (18.12)
The use of hydrazine is not subject to similar objections, but its slow reaction
with oxygen and partial decomposition into NH3 should be taken into account
in calculating proper dosages. Also, NH3 is a possible cause of stress-corrosion
cracking of copper-base alloys in the condenser system, should oxygen acciden-
tally contaminate the condensate.
REFERENCES
1. D. Pye, J. Am. Water Works Assoc. 39, 1121 (1947).

2. S. Pirt, D. Callow, and W. Gillett, Chem. Ind. (London) 1957, 730.
3. H. Gaunt and E. Wetton, J. Appl. Chem. 16, 171 (1966).
4. M. Baker and V. Marcy, Trans. Am. Soc. Mech. Eng. 78, 299 (1956).
5. B. P. Boffardi, Corrosion inhibitors in the water treatment industry, in ASM Hand-
book, Vol. 13A, Corrosion: Fundamentals, Testing, and Protection, ASM Interna-
tional, Materials Park, OH, 2003, p. 892.
6. See ASME Consensus on Operating Practices for the Control of Feedwater and Boiler
Water Quality in Modern Boilers, United Engineering Center, New York, 1979.
7. S. Matsuda, Sc.D. thesis, Department of Metallurgy, M.I.T., Cambridge, MA, 1960.
8. T. P. Hoar, in Third European Symposium on Corrosion Inhibitors, Università degli
Studi di Ferrara, Italy, 1971, p. 619.
9. Industrial Water Treatment Chemicals and Processes: Developments since 1978, M.
Collie, editor, Chemical Technology Review No. 217, Noyes Data Corp., Park Ridge,
NJ, 1983, pp. 36–42.
10. D. Robitaille and J. Bilek, Chem. Eng. 83(27), 77 (1976).
11. G. Mann, Brit. Corros. J. 12, 6 (1977).
12. D. Frey, Mater. Perf. 20(2), 49 (1981).
13. ASTM D807-05, Standard Practice for Assessing the Tendency of Industrial Boiler
Waters to Cause Embrittlement (USBM Embrittlement Detector Method), ASTM
International, West Conshohocken, PA.
14. E. Ulrich, in Passivierende Filme und Deckschichten, Anlaufschichten, H. Fischer, K.
Hauffe, and W. Wiederholt, editors, Springer, Berlin, 1956, p. 308.
15. V. Linnenbom, J. Electrochem. Soc. 105, 322 (1958).
16. G. Schikorr, Z. Elektrochem. 35, 65 (1929); Z. Anorg. Allgm. Chem. 212, 33 (1933).
17. P. Goldstein and C. Burton, Trans. Am. Soc. Mech. Engrs., Series A 91, 75 (1969).
18. G. Skaperdas and H. Uhlig, Ind. Eng. Chem. 34, 748 (1942).
19. Ref. 5, p. 893.
20. J. Dobson, Advances in Corrosion Science and Technology, Vol. 7, M. Fontana and
R. Staehle, editors, Plenum Press, New York 1980, p. 177.
21. H. Townsend, in Proceedings of the Fourth International Congress on Metallic
Corrosion, National Association of Corrosion Engineers, Houston, TX, 1972,
p. 477.
22. G. Mann, in High Temperature High Pressure Electrochemistry in Aqueous Solutions,
D. de G. Jones and R. Staehle, editors, National Association of Corrosion Engineers,
Houston, TX, 1976, p. 34.
23. H. Masterson, J. Castle, and G. Mann, Chem. Ind. (London) 1969, 1261.
GENERAL REFERENCES
B. P. Boffardi, Corrosion inhibitors in the water treatment industry, in ASM Handbook,

Vol. 13A, Corrosion: Fundamentals, Testing, and Protection, ASM International, Mate-
rials Park, OH, 2003, pp. 891–906.
Corrosion in fossil fuel power plants, in ASM Handbook, Vol. 13, Corrosion, ASM Inter-
national, Materials Park, OH, 1987, pp. 985–1010.
D. Frey, Case histories of corrosion in industrial boilers, Mater. Perf. 20(2), 49 (1981).
R. Garnsey, The chemistry of steam-generator corrosion, Combustion 52(2), 36 (1980).
High Temperature High Pressure Electrochemistry in Aqueous Solutions, D. de G. Jones
and R. Staehle, editors, National Association of Corrosion Engineers, Houston, TX,
1976.
G. R. Holcomb, Corrosion in supercritical water—Ultrasupercritical environments for

power production, in ASM Handbook, Vol. 13C, Corrosion: Environments and Indus-
tries, ASM International, Materials Park, OH, 2006, pp. 236–245.
R. M. Latanision and D. B. Mitton, Corrosion in supercritical water—Waste destruction
environments, in ASM Handbook, Vol. 13C, Corrosion: Environments and Industries,
G. Navitsky and F. Gabrielli, Boiler water treatment, feedwater treatment, and chemical
cleaning of drum-type utility steam generators, Combustion 52(2), 19 (1980).
19
ALLOYING FOR CORROSION
RESISTANCE; STAINLESS STEELS
19.1 INTRODUCTION
The development of alloys for controlling corrosion in specific aggressive envi-

ronments is certainly one of the great metallurgical developments of the twen-
tieth century. The basis upon which alloys resist corrosion and the causes of
corrosion susceptibility of alloys are explored in this and subsequent chapters.
In general, the corrosion behavior of alloys depends on the interaction of:
1. The alloy of specific chemical composition and metallurgical structure.

2. The film on the alloy surface.
3. The environment, whether it is sufficiently aggressive to break down the
protectiveness of the surface film, thereby initiating localized corrosion.
4. The alloy/environment combination, controlling whether the film self-
repairs after breakdown and, if not, the type and rate of corrosion that
propagates after initiation has occurred.
The beneficial effect of alloyed chromium or aluminum on the oxidation

resistance of iron has already been described (Section 11.11), in addition to the

333
334 ALLOYING FOR CORROSION RESISTANCE; STAINLESS STEELS
beneficial effect of small alloying additions of copper, chromium, or nickel on

atmospheric resistance (Section 9.5).
Alloys of gold with copper or silver retain the corrosion resistance of gold
above a critical alloy concentration called the reaction limit by Tammann [1].
Below the reaction limit, the alloy corrodes, for example, in strong acids, leaving
a residue of pure gold either as a porous solid or as a powder. This behavior of
noble-metal alloys is known as parting and is probably similar in mechanism to
dezincification of copper–zinc alloys (see Section 20.2.2).
Pickering and Wagner [2] proposed that the predominant mechanism of
parting in a gold–copper alloy containing, for example, 10 at.% Au occurs by
injection of divacancies at the corroding alloy surface that readily diffuse into
the alloy at room temperature and tend to fill with copper atoms. The latter
diffuse in the opposite direction toward the surface, where they enter into aqueous
solution. A mechanism involving dissolution of the alloy and subsequent rede-
position of gold is not likely because dissolved gold in any amount is not detected.
Instead, X-ray examination of the residual depleted porous layer shows that
interdiffusion of gold and copper takes place to form solid–solution alloys varying
in composition from that of the original alloy to pure gold. In other words,
the evidence supports solid-state diffusion of copper from within the alloy to
the surface, where it alone undergoes dissolution. Above the critical gold com-
position for parting, it is possible that conditions for divacancy formation are
no longer favorable, or perhaps the vacancies tend to fill with a higher proportion
of gold compared to copper atoms; hence, copper no longer corrodes
preferentially.
Various other noble-metal alloys (e.g., Pt–Ni, Pt–Cu, and Pt–Ag) also exhibit
reaction limits in HNO3. Corresponding alloy compositions vary with the corro-
sive medium, but reaction limits in general, whatever the environment, tend to
fall between 25 and 50 at.% of the noble-metal component (Table 19.1).
At higher temperatures, the same reaction limits apply, with the exception
that some attack may initiate above the reaction limit composition after long
exposure times. For example, at 100°C, exposure of the gold–silver alloys con-
taining more than 50 at.% Au for one or more weeks to nitric acid resulted in
measurable attack [3].
Rapid quenching of certain alloys consisting of, for example, iron, cobalt, or
nickel base and containing one or more metalloid additions, such as phosphorus,
TABLE 19.1. Reaction Limits [1]

Corrosive Medium Cu–Au Alloys Ag–Au Alloys
At.% Au Wt.% Au At.% Au Wt.% Au
(NH4)2S2 24.5–25.5 50.2–51.5 32 46.5

H2CrO4 50 75.5 49.2 63.9
HNO3 (specific gravity 1.3) 50 75.5 48.0–49.0 62.8–63.7
H2SO4 49–50 74.5–75.5 50 64.7
silicon, carbon, or boron, produces amorphous materials that are commonly

referred to as glassy alloys. Cooling from the liquid at rates of about 106 K degrees
per second “freezes” the atoms in nearly the same positions that they occupied
in the liquid [4]. More recently, alloys have been designed with glass-formation
cooling rates as low as 1 K/s [5]. As a result of their amorphous state, these alloys
do not have the long-range order that is characteristic of crystalline materials.
Instead, these materials are chemically and structurally homogeneous, without
defects, multiple phases, and grain boundaries, so that the corrosion resistance
may be much greater than that of crystalline alloys of the same composition.
Some of the glassy-alloy compositions are especially resistant to acid media,
including HCl and oxidizing solutions (e.g., FeCl3). Chromium, if present, may
be above or below 12%.
Alloying is an especially effective means for improving corrosion resistance
if passivity results from the combination of a metal, otherwise active, with a
normally passive metal. The alloying element may reduce either icritical [e.g., chro-
mium alloyed with iron (Fig. 6.11, Section 6.8)], or ipassive [e.g., nickel alloyed with
copper (Fig. 6.14, Section 6.8.1)]. For >12% Cr–Fe alloys, icritical is reduced to such
small values that any small corrosion current exceeds icritical and accounts for ini-
tiation of passivity in aerated aqueous solutions. Similarly, if passivity results
from a noble metal added in small amount to an active metal or alloy, the cor-
rosion rate may be reduced by orders of magnitude. The noble metal stimulates
the cathodic reaction and, in this way, increases the anodic current density to the
critical value for passivation. Practical examples are palladium or platinum
alloyed with stainless steels or with titanium (see Sections 6.4 and 25.3), which
resist sulfuric acid at concentrations and temperatures otherwise extremely cor-
rosive. Carbon in steel can act similarly by creating cathodic sites of cementite
(Fe3C) on which reduction of HNO3 (or HNO2 in HNO3) proceeds rapidly, allow-
ing passivity to establish itself in less concentrated acid than is the case for pure
iron. In principle, second phases of any kind (e.g., intermetallic compounds) can
induce passivity in multicomponent alloys by the same mechanism.
In homogeneous single-phase alloys, passivity usually occurs at and above a
composition that is specific to each alloy and that depends on the environment,
as explained in Section 6.8. For Ni–Cu alloys, the critical composition is 30–40%
Ni; for Cr–Co, Cr–Ni, and Cr–Fe alloys, it is 8%, 14%, and 12% Cr, respectively.
The stainless steels are ferrous alloys that contain at least 10.5% Cr. Stainless
steels are passive in many aqueous media, similar to the passivity of pure chro-
mium itself, and they are the most important of the passive alloys.
19.2 STAINLESS STEELS
Stainless steels depend on the integrity of a thin passive film to maintain low
corrosion rates in aqueous solutions. Any breakdown of this film is likely to result
in localized corrosion, at pits and crevices. Stress-corrosion cracking may also
occur. A wide range of stainless steels have been developed for applications in
many environments. In this section, the properties and behavior of stainless steels
are reviewed, and the principles for successful use of these important alloys are
described.
19.2.1 Brief History*

In 1820, J. Stodart and M. Faraday in England published a report [6] on the cor-
rosion resistance of various iron alloys they had prepared; apparently, it was this
report in which the chromium–iron alloys were first mentioned. The maximum
chromium content, however, was below that required for passivity, and they nar-
rowly missed discovering the stainless steels. In France in 1821, Berthier [7],
whose attention had been drawn to the work of Stodart and Faraday, found that
iron alloyed with considerable chromium was more resistant to acids than was
unalloyed iron. His alloys were obtained by direct reduction of the mixed oxides,
producing what today is called ferrochromium (40–80% Cr). The alloys were
brittle and were high in carbon, and they had no value as structural materials.
Berthier prepared some steels using ferrochromium as a component, but the
chromium content again was too low to overlap the useful passive properties
characteristic of the stainless steels.
Although a variety of chromium–iron alloys was produced in subsequent
years by several investigators who took advantage of the high-strength and high-
hardness properties imparted by chromium, the inherent corrosion resistance
of the alloys was not observed, largely because the accompanying high carbon
content impaired corrosion resistance. In 1904, Guillet [8] of France produced
low-carbon chromium alloys overlapping the passive composition range. He
studied the metallurgical structure and mechanical properties of the Cr–Fe alloys
and also of the Cr–Fe–Ni alloys that are now called austenitic stainless steels.
But recognition of the outstanding property of passivity in such alloys, initiating
at a minimum of 12% Cr, was apparently first described by Monnartz [9] of
Germany, who began his research in 1908 and published a detailed account of
the chemical properties of Cr–Fe alloys in 1911. This research included a descrip-
tion of the beneficial effect of oxidizing compared to reducing environments on
corrosion resistance, the necessity of maintaining low carbon contents, and the
effects of small quantities of alloying elements (e.g., Ti, V, Mo, and W).
The commercial utility of the Cr–Fe hardenable stainless steels as possible
cutlery materials was recognized in about 1913 by H. Brearley of Sheffield,
England. Looking for a better gun-barrel lining, he noticed that the 12%
Cr–Fe alloys did not etch with the usual nitric acid etching reagents and that they
did not rust over long periods of exposure to the atmosphere. The austenitic
Cr–Fe–Ni stainless steels, on the other hand, were first exploited in Germany in
1912–1914 based on research of E. Maurer and B. Strauss of the Krupp Steel
Works.
*Based largely on the account by Carl Zapffe, in Stainless Steels, American Society for Metals,
Cleveland, OH, 1949, pp. 5–25.
The 18% Cr, 8% Ni (18–8) austenitic stainless steel is the most popular of
all the stainless steels now produced.
19.2.2 Classes and Types

There are five main classes of stainless steels, designated in accord with their
crystallographic structure. Each class consists of several alloys of somewhat dif-
fering composition having related physical, magnetic, and corrosion properties.
These were given type numbers by the American Iron and Steel Institute (AISI).
Although AISI stopped issuing designations for new stainless steels several
decades ago, the AISI numbers remain in use today. The Unified Numbering
System (UNS) was introduced in the 1970s to include all alloys, including stain-
less steels. A listing of many stainless steels that are produced commercially is
given in Table 19.2.
The five main classes of stainless steels are martensitic, ferritic, austenitic,
precipitation-hardenable, and duplex.
1. Martensitic. The name of the first class derives from the analogous mar-
tensite phase in carbon steels. Martensite is produced by a shear-type
phase transformation on cooling a steel rapidly (quenching) from the
austenite region (face-centered cubic structure) of the phase diagram. It
is the characteristically hard component of quenched carbon steels, as well
as of the martensitiic stainless steels. In stainless steels, the structure is
body-centered cubic, and the alloys are magnetic. Typical applications
include cutlery, steam turbine blades, and tools.
2. Ferritic. Ferritic steels are named after the analogous ferrite phase, or
relatively pure-iron component of carbon steels cooled slowly from the
austenite region. The ferrite, or alpha, phase for pure iron is the stable
phase existing below 910 °C. For low-carbon Cr−Fe alloys, the high-
temperature austenite (or gamma) phase exists only up to 12% Cr; above
this Cr content, the alloys are ferritic at all temperatures up to the melting
point. They can be hardened moderately by cold working, but not by heat
treatment. Ferritic stainless steels are body-centered cubic in structure
and are magnetic. Uses include trim on autos and applications in synthetic
nitric acid plants.
3. Austenitic. Austenitic stainless steels are named after the austenite, or γ,
phase, which, for pure iron, exists as a stable structure between 910 °C and
1400 °C. This phase is face-centered cubic and nonmagnetic, and it is
readily deformed. It is the major or only phase of austenitic stainless steels
at room temperature, existing as a stable or metastable structure depend-
ing on composition. Alloyed nickel is largely responsible for the retention
of austenite on quenching the commercial Cr–Fe–Ni alloys from high
temperatures, with increasing nickel content accompanying increased sta-
bility of the retained austenite. Alloyed Mn, Co, C, and N also contribute
TABLE 19.2. Types and Compositions of Stainless Steels 338
AISI Type UNS Composition (%)

or Common No.
Name Cr Ni C Mn P (max) S (max) Si Other Remarks
(max) Elements
Class: Martensitic—Body-Centered Tetragonal, Magnetic, Heat-Treatable
403 S40300 11.5–13.0 — 0.15 max 1.0 0.04 0.03 0.5 Turbine quality
410 S41000 11.5–13.5 — 0.15 max 1.0 0.04 0.03 1.0
414 S41400 11.5–13.5 1.25–2.5 0.15 max 1.0 0.04 0.03 1.0
416 S41600 12.0–14.0 — 0.15 max 1.25 0.06 0.15 min 1.0 0.6 Mo max Easy machining,
nonseizing
416Se S41623 12.0–14.0 — 0.15 max 1.25 0.06 0.06 1.0 0.15 Se min Easy machining,
nonseizing
420 S42000 12.0–14.0 — Over 0.15 1.0 0.04 0.03 1.0
431 S43100 15.0–17.0 1.25–2.5 0.20 max 1.0 0.04 0.03 1.0
440A S44002 16.0–18.0 — 0.6–0.75 1.0 0.04 0.03 1.0 0.75 Mo
max
440B S44003 16.0–18.0 — 0.75–0.95 1.0 0.04 0.03 1.0 0.75 Mo
max
440C S44004 16.0–18.0 — 0.95–1.2 1.0 0.04 0.03 1.0 0.75 Mo Highest
max attainable
hardness
Class: Ferritic—Body-Centered Cubic; Magnetic, not Heat-Treatable

405 S40500 11.5–14.5 — 0.08 max 1.0 0.04 0.03 1.0 0.1–0.3 Al.
430 S43000 16.0–18.0 — 0.12 max 1.0 0.04 0.03 1.0
430F S43020 16.0–18.0 — 0.12 max 1.25 0.06 0.15 min 1.0 0.6 Mo max Easy machining,
nonseizing
430FSe S43023 16.0–18.0 — 0.12 max 1.25 0.06 0.06 1.0 0.15 Se min Easy machining,
ALLOYING FOR CORROSION RESISTANCE; STAINLESS STEELS
nonseizing
or Common No.
(max) Elements
446 S44600 23.0–27.0 — 0.20 max 1.5 0.04 0.03 1.0 0.25 N max Resistant to high-
temperature
oxidation
Class: Austenitic—Face-Centered Cubic, Nonmagnetic, not Heat-Treatable

STAINLESS STEELS
201 S20100 16.0–18.0 3.5–5.5 0.15 max 5.5–7.5 0.06 0.03 1.0 0.25 N max
202 S20200 17.0–19.0 4.0–6.0 0.15 max 7.5–10 0.06 0.03 1.0 0.25 N max
301 S30100 16.0–18.0 6.0–8.0 0.15 max 2.0 0.045 0.03 1.0
302 S30200 17.0–19.0 8.0–10.0 0.15 max 2.0 0.045 0.03 1.0
302B S30215 17.0–19.0 8.0–10.0 0.15 max 2.0 0.045 0.03 2.0–3.0 Resistant to high-
temperature
oxidation
303 S30300 17.0–19.0 8.0–10.0 0.15 max 2.0 0.20 0.15 min 1.0 0.6 Mo max Easy machining,
nonseizing
303 Se S30323 17.0–19.0 8.0–10.0 0.15 max 2.0 0.20 0.06 1.0 0.15 Se min Easy machining,
nonseizing
304 S30400 18.0–20.0 8.0–10.5 0.08 max 2.0 0.045 0.03 1.0
304L S30403 18.0–20.0 8.0–12.0 0.03 max 2.0 0.045 0.03 1.0 Extra-low carbon
305 S30500 17.0–19.0 10.5–13.0 0.12 max 2.0 0.045 0.03 1.0 Lower rate of
work hardening
than 302 or 304
308 S30800 19.0–21.0 10.0–12.0 0.08 max 2.0 0.045 0.03 1.0
309 S30900 22.0–24.0 12.0–15.0 0.20 max 2.0 0.045 0.03 1.0
309 S S30908 22.0–24.0 12.0–15.0 0.08 max 2.0 0.045 0.03 1.0
310 S31000 24.0–26.0 19.0–22.0 0.25 max 2.0 0.045 0.03 1.5
310 S S31008 24.0–26.0 19.0–22.0 0.08 max 2.0 0.045 0.03 1.5
314 S31400 23.0–26.0 19.0–22.0 0.25 max 2.0 0.045 0.03 1.5–3.0
316 S31600 16.0–18.0 10.0–14.0 0.08 max 2.0 0.045 0.03 1.0 2.0–3.0 Mo
316L S31603 16.0–18.0 10.0–14.0 0.03 max 2.0 0.045 0.03 1.0 2.0–3.0 Mo Extra-low carbon
317 S31700 18.0–20.0 11.0–15.0 0.08 max 2.0 0.045 0.03 1.0 3.0–4.0 Mo
321 S32100 17.0–19.0 9.0–12.0 0.08 max 2.0 0.045 0.03 1.0 Ti: 5 × Stabilized grade
339
C min
TABLE 19.2. Continued
340
or Common No.
(max) Elements
347 S34700 17.0–19.0 9.0–13.0 0.08 max 2.0 0.045 0.03 1.0 Cb + Ta: 10 Stabilized grade
× C min
348 S34800 17.0–19.0 9.0–13.0 0.08 max 2.0 0.045 0.03 1.0 Cb + Ta: 10 Stabilized grade
× C min 0.1 Ta max
0.20 Co when radiation
max conditions
require low Ta
Class: Precipitation-Hardenable
15–5 PH S15500 14.00–15.5 3.50–5.50 0.07 1.00 0.04 0.03 1.00 2.5–4.5 Cu
0.15–0.45
Nb
17–7 PH S17700 16.0–18.0 6.50–7.75 0.09 1.00 0.04 0.04 1.00 0.75–1.50
Al
Class: Daplex—Austenitic/Ferritic
2205 S32205 21.0–23.0 4.5–6.5 0.03 max 2.0 0.03 0.02 1.0 2.5–3.5 Mo
0.014–0.2 N
2304 S32304 21.5–24.5 3.0–5.5 0.03 max 2.5 0.04 0.04 1.0 0.05–0.6
Mo
0.05–0.6 Cu
0.05–0.2 N
Zeron 100 S32760 24.0–26.0 6.0–8.0 0.03 max 1.0 0.03 0.01 1.0 3.0–4.0 Mo
0.50–1.00
Cu
0.50–1.00
ALLOYING FOR CORROSION RESISTANCE; STAINLESS STEELS
W
0.20–0.30 N
to the retention and stability of the austenite phase. Austenitic stainless

steels can be hardened by cold working, but not by heat treatment. On
cold working, but not otherwise, the metastable alloys (e.g., 201, 202, 301,
302, 302B, 303, 303Se, 304, 304L, 316, 316L, 321, 347, 348; see Table 19.2)
transform in part to the ferrite phase (hence, the descriptor, “metastable”)
having a bond-centered-cubic structure that is magnetic. This transforma-
tion also accounts for a marked rate of work hardening. Alloys 305, 308,
309, and 309 S, on the other hand, work harden at a relatively low rate
and become only slightly magnetic, if at all. Alloys containing higher
chromium and nickel (e.g., 310, 310 S, 314) are essentially stable austenitic
alloys and do not transform to ferrite or become magnetic when deformed.
Uses of austenitic stainless steels include general-purpose applications,
architectural and automobile trim, and various structural units for the
food and chemical industries.
4. Precipitation Hardenable. The precipitation-hardening stainless steels
achieve high strength and hardness through low-temperature heat treat-
ment after quenching from high temperatures. These Cr–Fe alloys contain
less nickel (or none) than is necessary to stabilize the austenite phase, and,
in addition, they contain alloying elements, such as aluminum or copper,
that produce high hardness through formation and precipitation of inter-
metallic compounds along slip planes or grain boundaries. They are
applied whenever the improved corrosion resistance imparted by alloyed
nickel is desirable, or, more important, when hardening of the alloy is best
done after machining operations, using low-temperature heat treatment
[e.g., 480°C (900°F)] rather than a high-temperature quench as is required
in the case of the martensitic stainless steels.
5. Duplex. The duplex stainless steels contain both austenite and ferrite,
typically with the austenite:ferrite ratio ∼ 60 : 40. The mixed austenite–
ferrite microstructure, consisting of a continuous ferrite matrix with aus-
tenite islands (Fig. 19.1 [10]), is achieved by including in the composition
a balance of elements that stabilize austenite (e.g., nickel and nitrogen)
and those that stabilize ferrite (e.g., chromium and molybdenum). The
22% chromium duplex stainless steel was developed in the late 1970s and
was later modified and designated as Alloy 2205 (UNS designation
S32205). Because of good mechanical properties, high resistance to chlo-
ride stress-corrosion cracking, good erosion and wear resistance, and low
thermal expansion, duplex stainless steels are used in many applications,
including pressure vessels, storage tanks (e.g., for phosphoric acid), and
heat exchangers [10]. For seawater service, duplex stainless steels of higher
molybdenum content (e.g., Zeron 100) have been developed [11].
In general, the highest resistance to uniform corrosion is obtained with the

nickel-bearing austenitic types, and, in general, the highest nickel-composition
alloys in this class are more resistant than the lowest nickel compositions. For
Figure 19.1. Typical microstructure of a duplex stainless steel. The grains are elongated in
the rolling direction (∼300×) [10]. (Reprinted with permission of John Wiley & Sons, Inc.)
optimum corrosion resistance, austenitic alloys must be quenched (rapidly cooled

by water or by an air blast) from about 1050–1100°C (1920–2000°F). The molyb-
denum-containing austenitic alloys (316, 316L, 317) have improved corrosion
resistance to chloride-containing environments, dilute nonoxidizing acids, and
crevice corrosion.
The ferritic stainless steels have optimum corrosion resistance when cooled
slowly from above 925°C (1700°F) or when annealed at 650−815°C (1200−1500°F).*
Recently developed ferritic stainless steels of controlled purity contain molybde-
num additions and low carbon and nitrogen. Typical analyses include 26% Cr,
1% Mo, <0.01% C, <0.02% N; 18% Cr, 2% Mo, <0.025% C, <0.025% N; 28%
Cr, 4% Mo, <0.01% C, <0.02% N. Alloyed titanium or columbium is sometimes
included in the first two alloys in order to raise the tolerable carbon and nitrogen
contents. All these alloys can be quenched from above 925 °C without loss of
corrosion resistance. Their corrosion properties are generally better than those
of the conventional ferritic, and some austenitic, stainless steels listed in Table
19.2—for example, in NaCl solutions, HNO3, and various organic acids, provided
they retain passivity. Should they lose passivity, locally or generally, their corro-
sion rates tend to be higher than those of the active nickel-containing austenitic
stainless steels of equivalent chromium and molybdenum contents [12].
The martensitic stainless steels, on the other hand, have optimum corrosion
resistance as quenched from the austenite region. In this state, they are very hard
and brittle. Ductility is improved by annealing (650–750°C for 403, 410, 416,
*For additional details on heat treating stainless steels, see ASM Handbook, Vol. 4, Heat Treating,
ASM International, Materials Park, OH, 1991, pp. 769−792.
416Se; 650–730°C for 414; 620–700°C for 431; 680–750°C for 440 A, B, C, and
420), but at some sacrifice of corrosion resistance. Resistance to pitting and
rusting in 3% NaCl at room temperature reaches a minimum after tempering a
0.2–0.3% C, 13% Cr stainless steel at 500°C, as well as 650°C for a similar steel
containing 0.06% C [13]. In general, the tempering range 450–650°C (840–1200°F)
should be avoided if possible. Decrease of corrosion resistance probably results,
in part, from the transformation of martensite containing interstitial carbon into
a network of chromium carbides attended by depletion of chromium in the
adjoining metallic phase.
Cold working any of the stainless steels usually has only minor effect on
uniform corrosion resistance if temperatures are avoided that are high enough
to permit appreciable diffusion during or after deformation. Phase changes
brought about by cold working the metastable austenitic alloys are not accom-
panied by major changes in corrosion resistance.* Furthermore, quenched aus-
tenitic stainless steel (face-centered cubic) of 18% Cr, 8% Ni composition has
approximately the same corrosion resistance as quenched ferritic stainless steel
(body-centered cubic), of the same chromium and nickel composition but with
lower carbon and nitrogen content [14]. However, if a similar alloy containing a
mixture of austenite and ferrite is briefly heated at, for example, 600°C, composi-
tion differences are established between the two phases setting up galvanic cells
that accelerate corrosion. Composition gradients, whatever their cause, are more
important in establishing uniform corrosion behavior than are structural varia-
tions of an otherwise homogeneous alloy. This statement is true for metals and
alloys in general.
19.2.3 Intergranular Corrosion

Improper heat treatment of ferritic or austenitic stainless steels causes the grain
boundaries, which separate the individual crystals, to become especially suscep-
tible to corrosion. Corrosion of this kind leads to catastrophic reduction in
mechanical strength. The specific temperatures and times that induce susceptibil-
ity to intergranular corrosion are called sensitizing heat treatments. They are very
much different for the ferritic and the austenitic stainless steels. In this respect,
the transition in sensitizing temperatures for steels containing 18% Cr occurs at
about 2.5–3% Ni [15]; stainless steels containing less than this amount of nickel
are sensitized in the temperature range typical of nickel-free ferritic steels,
whereas those containing more nickel respond to the temperature range typical
of the austenitic stainless steels.
19.2.3.1 Austenitic Stainless Steels. For austenitic alloys, the sensitizing

temperature range is approximately 425–875°C (800–1610°F). The degree of
*After transformation, the alloys, otherwise resistant, become susceptible to hydrogen cracking; also,
ferritic and martensitic stainless steels on cold working tend to become more susceptible to hydrogen
cracking.
damage to commercial alloys caused by heating in this range depends on time,

with a few minutes at the higher temperature range of 750°C (1380°F) being
equivalent to several hours at a lower (or still higher) temperature range (Fig.
19.2) [16, 17]. Slow cooling through the sensitizing temperature range or pro-
longed welding operations induce susceptibility, but rapid cooling avoids damage.
Hence, austenitic stainless steels must be quenched from high temperatures. Spot
welding, in which the metal is rapidly heated by a momentary electric current
followed by a naturally rapid cooling, does not cause sensitization. Arc welding,
on the other hand, can cause damage, with the effect being greater the longer
the heating time, especially when heavy-gage material is involved. Sensitizing
temperatures are reached some millimeters away from the weld metal itself, with
the latter being at the melting point or above. Hence, on exposure to a corrosive
environment, failure of an austenitic stainless steel weld—called weld decay—
occurs in zones slightly away from the weld rather than at the weld itself (see
Fig. 19.3).
The extent of sensitization for a given temperature and time depends very
much on carbon content. An 18–8 stainless steel containing 0.1% C or more may
be severely sensitized after heating for 5 min at 600°C, whereas a similar alloy
containing 0.06% C is affected less, and for 0.03% C the alloy heat treated simi-
larly may suffer no appreciable damage on exposure to a moderately corrosive
environment. The higher the nickel content of the alloy, the shorter the time for
sensitization to occur at a given temperature, whereas alloying additions of
molybdenum increase the time [16].
The physical properties of stainless steels after sensitization do not change
greatly. Because precipitation of carbides accompanies sensitization, the alloys
become slightly stronger and slightly less ductile. Damage occurs only on expo-
sure to a corrosive environment, with the alloy corroding along grain boundaries
at a rate depending on severity of the environment and the extent of sensitiza-
tion. In seawater, a sensitized stainless-steel sheet may fail within weeks or
Figure 19.2. Effect of time and temperature on sensitization of 18.2% Cr, 11.0% Ni,
0.05% C, 0.05% N stainless steel [16]. (Reprinted with permission of ASM International®.
All rights reserved. www.asminternational.org.)
Intergranular corrosion
Weld
Figure 19.3. Example of weld decay (2×). After sensitization, specimen was exposed to 25%
HNO3.
months; but in a boiling solution containing CuSO4·5H2O (13 g/liter) and H2SO4
(47 mL concentrated acid/liter), which is used as an accelerated test medium,
failure occurs within hours.
19.2.3.2 Theory and Remedies. Since intergranular corrosion of austenitic

stainless steels is associated with carbon content, a low-carbon alloy (<0.02% C)
is relatively immune to this type of corrosion [18]. Nitrogen, normally present in
commercial alloys to the extent of a few hundredths percent, is less effective than
carbon in causing damage (Fig. 19.4) [19]. At high temperatures [e.g., 1050°C
(1920 °F)], carbon is almost completely dispersed throughout the alloy, but within
(or somewhat above) the sensitizing temperature range it rapidly diffuses to the
grain boundaries where it combines preferentially with chromium to form chro-
mium carbides (e.g., M23C6, in which M represents the presence of some small
amount of iron along with chromium). This reaction depletes the adjoining alloy
of chromium to the extent that the grain-boundary material may contain less
than the 12% Cr necessary for passivity. The affected volume of alloy normally
extends some small distance into the grains on either side of the boundary itself,
causing apparent grain-boundary broadening of the etched surface. The chro-
mium-depleted alloy sets up passive–active cells of appreciable potential differ-
ence, with the grains constituting large cathodic areas relative to small anodic
areas at the grain boundaries. Electrochemical action results in rapid attack along
the grain boundaries and deep penetration of the corrosive medium into the
interior of the metal.
If the alloy is rapidly cooled through the sensitizing zone, carbon does not
have time either to reach the grain boundaries or to react with chromium if some
carbon is already concentrated at the grain boundaries. On the other hand, if the
Figure 19.4. Intergranular corrosion measured by change in electrical resistance of 18–8

stainless steels containing nitrogen or carbon immersed in 10% CuSO4 + 10% H2SO4. All speci-
mens sensitized at stated temperatures for 217 h [19]. (Reproduced with permission. Copyright
1945, The Electrochemical Society.)
alloy remains within the sensitizing temperature zone an especially long time
(usually several thousand hours), chromium again diffuses into the depleted
zones, reestablishing passivity of the grain boundaries and eliminating suscepti-
bility to preferred attack. Although nitrogen forms chromium nitrides, it is less
effective than carbon in causing damage, perhaps in part because nitrides pre-
cipitate more generally throughout the grains or they form islands along grain
boundaries, interrupting a continuous path along which the corrosive agent can
proceed [19]. Carbides, on the other hand, form continuous paths of chromium-
depleted alloy.
Other experimental data can be cited that supports the chromium-depletion
mechanism of intergranular corrosion of austenitic stainless steels. For example,
carbides isolated from grain boundaries of sensitized stainless steels have shown
an expected high chromium content. Along the same lines, corrosion products
of grain-boundary alloy obtained by choosing corrosive conditions that avoid
attack of carbides show a lower chromium content than corresponds to the alloy.
In this respect, Schafmeister [20], using cold concentrated sulfurous acid acting
on sensitized 18% Cr, 8.8% Ni, 0.22% C stainless steel for 10 days, found only
8.7% Cr in the alloy that had corroded from grain-boundary regions. Accompa-
nying analyses for Ni and Fe of 8.4% and 83%, respectively, showed no appre-
ciable depletion in nickel and an increase in iron content.
Microprobe scans of sensitized stainless steels have indicated chromium
depletion and nickel enrichment at grain boundaries [21]. Radioactive C14 intro-
duced into an austenitic 18% Cr, 12.8% Ni, 0.12% C stainless steel has demon-
strated enrichment of carbon at grain boundaries observable immediately after

quenching from 1000 °C to 1350 °C. This indicates that time for sensitization may
depend, in part, on the reaction rate of chromium with carbon already at grain
boundaries and not alone on the time required for additional carbon to diffuse
to grain boundaries.
There are at least three effective means for avoiding susceptibility to inter-
granular corrosion:
1. Heat Treatment at 1050−1100°C (1920−2000°F) Followed by Quenching.

At high temperature, precipitated carbides are dissolved, and rapid cooling pre-
vents their re-formation. This treatment is recommended, for example, after
welding operations. It is not always a possible treatment, however, because
of the size of the welded structure or because of a tendency of the alloy to warp
at high temperatures.
2. Reduction of Carbon Content. Carbon content can be reduced in the

commercial production of stainless steels, but at extra cost. Alloys of low carbon
content (e.g., <0.03% C) are designated by letter L—for example, Types 304L
and 316L. These alloys can be welded or otherwise heated in the sensitizing
temperature range with much less resultant susceptibility to intergranular corro-
sion. However, they are not immune.
3. Addition of Titanium or Niobium (Columbium). By alloying austenitic

alloys with a small amount of an element (e.g., Ti or Nb) having higher affinity
for carbon than does chromium, carbon is restrained from diffusing to the grain
boundaries, and any which is already at the boundary reacts with titanium or
columbium instead of with chromium. Alloys of this kind are called stabilized
grades (e.g., Types 321, 347, 348). Except as noted below, they can be welded or
otherwise heated within the sensitizing zone without marked susceptibility to
intergranular corrosion. Optimum resistance to intergranular corrosion at 675°C
(1250°F) is obtained by a prior carbide stabilizing heat treatment for several hours
at about 900°C (1650°F) [17, 22]. This heat treatment converts available carbon
to stable carbides of titanium or niobium in a temperature range of lower carbon
solubility compared to that of the usual higher quench temperatures.
In welding operations, the weld rod usually contains niobium rather than
titanium; the latter tends to oxidize at elevated temperatures with the danger of
its residual concentration becoming too low to stabilize the weld alloy against
corrosion. Niobium, on the other hand, is lost by oxidation to a lesser extent.
If, during welding the stabilized grades of stainless steel, the region of the
base metal adjacent to the weld is heated to temperatures at which the carbides
of titanium and niobium dissolve [above about 1230°C (2250°F)] and the cooling
rate is sufficiently rapid to prevent the formation of the stabilizing carbides, then
these steels can be sensitized if they are subsequently heated in the temperature
range in which chromium carbides precipitate. In such a situation, a narrow
region immediately adjacent to the weld is susceptible to intergranular corrosion,
which, if it occurs, is called knife-line attack. This type of intergranular corrosion

can be prevented by selecting the welding process parameters to avoid tempera-
tures at which carbides of titanium and niobium dissolve and by using a carbide-
stabilizing heat treatment as described above.
19.2.3.3 Intergranular Corrosion of Nonsensitized Alloys. Sigma phase

is a hard, brittle, intermetallic compound, rich in chromium and molybdenum,
with a tetragonal structure that can precipitate at grain boundaries in Type 316
stainless steel when heated in the range 540–1000 °C (1000–1800°F). Sigma phase
impairs corrosion resistance in highly oxidizing nitric acid environments. The
mechanism of corrosion may be based on the high molybdenum content of sigma
phase, which results in preferential direct attack on the sigma phase particles in
preference to the molybdenum-depleted zones surrounding them [23].
Sigma phase may also form in Types 310, 430, and 446 stainless steels, but
in these alloys the phase forms at a rate so low that it is important only when the
alloys are used in the temperature range in which sigma phase is formed [23].
In strongly oxidizing media (e.g., boiling 5N HNO3 + Cr6+), austenitic stain-
less steels, including stabilized grades, quenched from 1050°C, undergo slow
intergranular attack [24]. Stress is not necessary. The attack occurs only in the
transpassive region; hence, oxidizing ions, such as Cr6+ (0.1–0.5 N K2Cr2O7), Mn7+,
or Ce4+, are necessary additions to the boiling nitric acid. The rate of attack
increases with the amount of alloyed nickel [25], being more than 10 times higher
for a 78% Ni, 17% Cr, bal. Fe alloy compared to a similar 10% Ni alloy (70-h
test). This trend is opposite to the beneficial effect of nickel on the resistance of
stainless steels to stress-corrosion cracking.
Grain-boundary attack of 19% Cr, 9% Ni stainless steel is most rapid after
quenching from 1100°C to 1200°C; it is less pronounced on quenching from either
900°C or 1400°C [26]. High-purity alloys are immune. Alloyed carbon, nitrogen,
oxygen, or manganese added in small concentrations have no effect, whereas
silicon and phosphorus (>100 ppm) are damaging. Silicon causes increased inter-
granular attack in the intermediate range of 0.1−2% for the 14% Cr, 14% Ni
stainless steel; in larger or smaller amounts the alloy is not susceptible [27]. The
necessity of strongly oxidizing conditions and presence of phosphorus for inter-
granular attack was confirmed for a quenched low carbon 20% Cr, 20% Ni, 0.1%
P stainless steel [28]. When polarized anodically in 1 N H2SO4 or in 27% HNO3
at 40°C, intergranular attack occurred only at very noble potentials in the trans-
passive region. With only 0.002% P in the alloy, such attack was not observed at
any potential.
Similar intergranular attack of 15% Cr, 6% Fe, bal. Ni (Inconel 600) in high-
temperature water (350°C) or steam (600–650°C) [25] or of stabilized 18–8 stain-
less steel in potassium hydroxide solutions (pH 11) at 280°C [29] has been
reported. This matter is of prime interest in view of the common use of Inconel
600 and stainless steels in the construction of nuclear reactors for power produc-
tion. Contaminants in the water [such as traces of dissolved O2, NaOH, or dis-
solved lead (from heat-transfer tube–tube sheet leakage)], and the presence of
crevices at which superheating occurs accompanied by concentration of solute

accelerate S.C.C. [30]. Laboratory tests indicate that such failures also occur in
longer times in relatively pure water [31] (see also Section 23.3.3). Increased
nickel content favors intergranular corrosion [32] of 18–20% Cr stainless steels
at 200–300°C in water containing Cl− and dissolved oxygen, as it does in boiling
HNO3–Cr6+. Silicon (>0.3%) and phosphorus (>0.023%) in 14% Cr, 14% Ni stain-
less steel exposed to 0.01% FeCl3 at 340°C, analogous to results in HNO3 + Cr6+,
cause intergranular corrosion. Unlike the latter medium, the high-temperature
0.01% FeCl3 solution (21-day exposure) caused intergranular corrosion [33] of
the nonsensitized stainless steel when it contained >0.05% C.
The overall results confirm that intergranular attack is the result of specific
impurities in the alloy segregating at grain-boundary regions. The extent of their
damaging effect depends on the chemical environment to which the alloy is
exposed. Although applied stress has been stated to increase the observed attack
in various media, stress is not always necessary; hence, the observed damage in
such instances is better described as intergranular corrosion rather than as stress-
corrosion cracking.
19.2.3.4 Ferritic Stainless Steels. The sensitizing range for ferritic stainless
steels lies above 925°C (>1700°F), and immunity is restored by heating for a short
time (approximately 10–60 min) at 650–815°C (1200–1500°F). These tempera-
tures are the opposite of those applying to austenitic stainless steels. The same
accelerating media (i.e., boiling CuSO4–H2SO4 or 65% HNO3) produce inter-
granular corrosion in either class, and the extent and rapidity of damage are
similar. In welded sections, however, damage to ferritic steels occurs to metal
immediately adjacent to the weld and to the weld metal itself, whereas in aus-
tenitic steels the damage by weld decay localizes some small distance away from
the weld.
Chromium content of ferritic steels, whether high or low (16–28% Cr), has
no appreciable influence on susceptibility to intergranular corrosion [34]. Similar
to the situation for austenitic steels, lowering the carbon content is helpful, but
the critical carbon content is very much lower. A type 430 ferritic stainless steel
containing only 0.009%C was still susceptible [34]. Only on decarburizing low-
carbon steels containing 16% or 24% Cr in H2 at 1300°C for 100 h was immunity
obtained in the CuSO4–H2SO4 test solution [35]. Similarly, a low-carbon
(∼0.002%) 25% Cr–Fe alloy was reported to be immune [36]. Addition of tita-
nium in the amount of eight times carbon content or more provided immunity
to the CuSO4 test solution, but not to boiling 65% HNO3 [34].
Niobium additions, it was stated, behaved similarly, and only heat treatment,
as described previously, was effective in conferring immunity to nitric acid. It
was reported [37], however, that columbium additions (8× C + N content), but
not titanium additions, minimize the observed intergranular corrosion of welds
exposed to boiling 65% HNO3. This behavior may be explained by the observed
marked reactivity of titanium carbides, but not niobium carbides, with HNO3
along grain boundaries where such carbides are concentrated [38].
The Mo–Cr stainless steels of controlled purity, described earlier, although

in some instances containing more than 0.01% C, are immune to intergranular
corrosion. This is accounted for by their molybdenum content, which slows down
diffusion of carbon and nitrogen, and by their titanium or niobium content which,
if present, reacts preferentially with carbon and nitrogen.
Intergranular corrosion of ferritic stainless steels is best explained on the
basis of the chromium-depletion theory that is generally accepted for the austen-
itic stainless steels [39]. Differences in sensitization temperatures and times com-
pared to the austenitic steels are explained by the much higher diffusion rates of
carbon, nitrogen, and chromium in the ferritic body-centered-cubic lattice com-
pared to the austenitic face-centered-cubic lattice. Accordingly, chromium car-
bides and nitrides, in solution at higher temperatures, precipitate rapidly (within
seconds) below 950°C along grain boundaries, depleting the adjoining alloy
of chromium to resultant compositions below stainless-steel requirements and
which corrode at correspondingly higher rates than the grains. But accompanying
high diffusion rates of chromium account for restored immunity to intergranular
corrosion on heating the alloy for several minutes in the range 650–815°C (rather
than weeks or months required to restore sensitized austenitic stainless
steels), thereby restoring the grain-boundary alloy to normal stainless-steel
composition.
19.2.4 Pitting and Crevice Corrosion

In environments containing appreciable concentrations of Cl− or Br−, in which
stainless steels otherwise remain essentially passive, all the stainless steels
tend to corrode at specific areas and to form deep pits. Ions such as thiosulfate
( S2O32− ) may also induce pitting. In the absence of passivity, such as in deaerated
alkali-metal chlorides, nonoxidizing metal chlorides (e.g., SnCl2 or NiCl2), or
oxidizing metal chlorides at low pH, pitting does not occur. This holds even
though, in acid environments, general corrosion may be appreciable.
Stainless steels exposed to seawater develop deep pits within a matter of
months, with the pits usually initiating at crevices or other areas of stagnant
electrolyte (crevice corrosion). Susceptibility to pitting and crevice corrosion is
greater in the martensitic and ferritic steels than in the austenitic steels; it
decreases in the latter alloys as the nickel content increases. The austenitic 18–8
alloys containing molybdenum (types 316, 316L, 317) are still more resistant to
seawater; however, crevice corrosion and pitting of these alloys eventually
develop within a period of 1–2.5 years.
Stainless steels exposed at room temperature to chloride solutions containing
active depolarizing ions, such as Fe3+, Cu2+, or Hg2+, develop visible pits within
hours. These solutions have sometimes been used as accelerated test media to
assess pitting susceptibility.
Many extraneous anions, some more effective than others, act as pitting
inhibitors when added to chloride solutions. For example, as mentioned in Section
6.6, addition of 3% NaNO3 to a 10% FeCl3 solution completely inhibited pitting
of 18–8 stainless steel, as well as avoiding general attack, over a period of at least
25 years. Hence, so long as passivity does not break down at crevices because of
dissolved oxygen depletion, or for other reasons, localized corrosion does not
initiate in inhibited solutions no matter how long the time. Similarly, in neutral
chlorides (e.g., NaCl solutions), addition of alkalies inhibits pitting. In aerated
4% NaCl solution at 90°C, at which temperature the pitting rate of 18–8 is
highest, addition of 8 g NaOH per liter was found to eliminate pitting [40]. In
refrigerating brines, addition of 1% Na2CO3 was effective for at least 5 years
[41].
Pits develop more readily in a stainless steel that is metallurgically inhomo-
geneous. Similarly, the pitting tendency of an austenitic steel increases when the
alloy is heated briefly in the carbide precipitation (sensitization) range. Pitting
resulting from crevice corrosion is also favored whenever a stainless steel is
covered by an organic or inorganic film or by marine fouling organisms, which
partially shield the surface from access to oxygen. The movement of flowing
seawater tends to keep the entire surface in contact with aerated water and uni-
formly passive, reducing any tendency for localized corrosion.
19.2.4.1 Theory of Pitting. Pitting corrosion is usually considered to consist

of two stages:
1. Initiation, in which the integrity of the passive film is breeched at localized

areas and pits form.
2. Propagation of the pit, at a rate that is often found to increase with time,
because of the increasing acidity inside the pit.
The initiation of pits on an otherwise fully passive 18–8 surface, as discussed

earlier (Section 6.5.2), requires that the corrosion potential exceed the critical
potential [0.21 V(S.H.E.) in 3% NaCl]. The oxygen potential in air at pH 7 (0.8 V)
or the ferric–ferrous potential (φ° = 0.77 V) is sufficiently noble to induce pitting.
However, the stannic–stannous (φ° = 0.15 V) and the chromic–chromous poten-
tials (φ° = −0.41 V) are too active; hence, pitting of 18–8 stainless steels is
not observed in deaerated stannic or chromic chloride solutions. In sufficient
concentration, the nitrate ion shifts the critical potential to a value that is
noble to the ferric–ferrous oxidation–reduction potential; hence, pitting in
3% NaNO3 + 10% FeCl3 is not observed. Other anions shift the critical potential
similarly, with their effectiveness in this regard decreasing in the order
OH − > NO3− > SO24− > ClO4− . Increasing amounts of alloyed chromium, nickel,
molybdenum, and rhenium in stainless steels also shift the critical potential in
the noble direction, accounting for increased resistance to pitting.
In addition to the critical pitting potential (CPP) (noble to which pits initi-
ate), critical pitting temperatures (CPT) have been measured. Stable pitting
occurs at temperatures above the CPT [42]. Below this temperature, stable
pitting does not take place at any potential. The CPT has been explained as the
temperature below which the rapid dissolution required for pitting cannot take
place.
Once a pit initiates, a passive–active cell is set up of 0.5−0.6 V potential dif-
ference. The resultant high current density accompanies a high corrosion rate of
the anode (pit) and, at the same time, polarizes the alloy surface immediately
surrounding the pit to values below the critical potential. Through flow of current,
chloride ions transfer into the pit forming concentrated solutions of Fe2+, Ni2+,
and Cr3+ chlorides, which, by hydrolysis, account for an acid solution (Fig. 19.5).
The measured pH of the confined anodic corrosion products of 18–8 stainless
steel in 5% NaCl at 200 A/m2 (0.02 A/cm2) is 1.5 [43]. The high Cl− concentration
and low pH ensure that the pit surface remains active. At the same time, the high
specific gravity of such corrosion products causes leakage out of the pit in the
direction of gravity, inducing breakdown of passivity wherever the products
come into contact with the alloy surface. This accounts for a shape of pits elon-
gated in the direction of gravity, as is often observed in practice. An 18–8 stain-
less-steel sheet exposed to seawater for one year was observed to develop an
elongated narrow pit reaching 60 mm (2.5 in.) from its point of origin (Fig. 19.6).
The mechanism of growth was demonstrated in the laboratory [43] by continu-
ously flowing a fine stream of concentrated FeCl2 solution over an 18–8 surface
slightly inclined to the vertical and totally immersed in FeCl3, resulting in forma-
tion of a deep groove under the FeCl2 stream within a few hours (Fig. 19.6). A
similar groove does not form on an iron surface, because a passive–active cell is
not established.
A pit stops growing only if the surface within the pit is again passivated,
bringing the pit and the adjacent alloy to the same potential. Extraneous anions,
such as SO2− 4 , have no effect; on the other hand, dissolved oxygen or passivator
ions (e.g., NO−3 ) reinitiate passivity on entering a pit. Successful repassivation
depends on factors such as pit geometry and stirring rate.
The factors accounting for rates of corrosion at crevices follow the same
principles as those described for pit growth. The higher the electrolyte conductiv-
ity and the larger the cathode area outside the crevice, the higher the rate of
attack at the anode. The initiation of crevice corrosion, however, does not depend
Figure 19.5. Passive–active cell responsible for pit growth in stainless steel exposed to chlo-
ride solution.
(a) (b)
Figure 19.6. (a) Elongated pit in 18–8 stainless steel specimen 75 × 125 mm (3 × 5 in.) exposed
to Boston Harbor seawater for 1 year; pit began at crevice formed between bakelite rod and
interior surface of hole. (b) Artificial elongated pit formed by flowing 50% FeCl2 in a fine
stream over 18–8 stainless steel immersed in 10% FeCl3, 4 hr.
on exceeding the critical pitting potential. Instead, it depends only on factors

influencing the breakdown of passivity within the crevice. This breakdown may
occur, for example, by oxygen depletion in the crevice caused by slow uniform
alloy corrosion, followed by setting up a differential aeration cell that results in
accumulation of acid anodic corrosion products in the crevice. These changes in
electrolyte composition eventually destroy passivity, thereby establishing a still
larger potential difference between active metal in the crevice and passive metal
outside, analogous to cells operating in pitting corrosion. This mechanism for
initiation of crevice corrosion indicates that chlorides are not essential to its
occurrence, accounting for the observation that crevice corrosion occurs in solu-
tions of sulfates, nitrates, acetates, and so on, as well as of chlorides.
Cathodic protection effectively avoids crevice corrosion, provided that the
alloy surrounding the crevice is polarized to the open-circuit potential of the
active (nonpassive) alloy surface within the crevice. This contrasts with the more
lenient requirement of polarizing below the critical potential in order to avoid
pit initiation.
Alloy additions that are effective in helping retain passivity in the presence
of both low dissolved oxygen concentration and acid corrosion products help
reduce or avoid crevice attack. Additions of molybdenum to 18–8 stainless steel
(type 316) and palladium additions to titanium (see Fig. 25.2, Section 25.2) are
in this category.
19.2.4.2 Reducing or Avoiding Pitting Corrosion. There are four princi-

pal ways of reducing or avoiding pitting corrosion:
1. Cathodically protect at a potential below the critical pitting potential. An

impressed current can be used; or in good conducting media (e.g., sea-
water), stainless steel can be coupled to an approximately equal or greater
area of zinc, iron, or aluminum [44]. Austenitic stainless steels used to
weld mild-steel plates, or 18–8 propellers on steel ships, do not pit.
2. Add extraneous anions (e.g., OH− or NO−3 ) to chloride environments.
3. Reduce oxygen concentration of chloride environments (e.g., NaCl
solutions).
4. For type 304, operate at the lowest temperature possible.*
19.2.4.3 Reducing or Avoiding Crevice Corrosion. There are three ways

to reduce or avoid crevice corrosion:
1. Avoid crevices between metals or between metals and nonmetals. Periodi-

cally remove contaminating surface films using alkaline cleaners with
stainless-steel wool or the equivalent.
2. Avoid stagnant solutions. Circulate, stir, and aerate electrolytes in contact
with stainless steels. Ensure uniform composition of electrolyte at all
regions of the metal surface.
3. Cathodically protect, ideally to the potential of corroding active metal at
the crevice. Approaching such a potential reduces the corrosion rate, but
not to zero. In seawater, use of sacrificial iron and similar less-noble-metal
anodes have proved useful [45].
19.2.5 Stress-Corrosion Cracking and Hydrogen Cracking

In the presence of an applied or residual tensile stress, stainless steels may crack
transgranularly when exposed to certain environments (Fig. 19.7). Compressive
stresses, to the contrary, are not damaging. The higher the tensile stress, the
shorter is the time to failure. Although at low stress levels, time to cracking may
be long, there is, in general, no practical minimum stress below which cracking
will not occur, given sufficient time in a critical environment.
Damaging environments that cause cracking may differ for austenitic, com-
pared to martensitic or ferritic, stainless steels. For austenitic steels, the two
major damaging ions are hydroxyl and chloride (OH− and Cl−). A boiling, rela-
tively concentrated chloride that hydrolyzes to a slightly acid pH, such as FeCl2
or MgCl2, can cause cracking of thick sections of stressed 18–8 within hours. A
*In aerated 4% NaCl, maximum weight loss by pitting occurs at 90°C. [H. Uhlig and M. Morrill, Ind.
Eng. Chem. 33, 875 (1941)]. To avoid S.C.C. and to minimize pitting, operating temperatures in NaCl
solutions should be kept below 60–80°C.
Figure 19.7. Stress-corrosion cracking of 18–8, type 304 stainless steel exposed to calcium
silicate insulation containing 0.02–0.5% chlorides, 100°C (250×). Note that the cracks for this
environment start at a pit. An undulating path accounts for disconnected cracks as viewed in
one plane [47]. (Copyright ASTM International. Reprinted with permission.)
solution of concentrated MgCl2 boiling at about 154°C, for example, is used as

an accelerated test medium. The presence of dissolved oxygen in such solutions
is not necessary for cracking to occur, but its availability hastens damage, as does
the presence of oxidizing ions, such as Fe3+. Pitting is not a preliminary require-
ment for initiation of cracks. In NaCl and similar neutral solutions, on the other
hand, cracking of austenitic stainless steels is observed only if dissolved oxygen
or other oxidizing agent is present [46], and the amount of chloride needed to
cause damage can be extremely small (Fig. 19.8). Cracking of 18–8 stainless tubes
in heat exchangers has been observed in practice after contact with cooling
waters containing 25 ppm Cl− or less, and cracking has also been induced by small
amounts of chlorides contained in magnesia insulation wrapped around stainless-
steel tubes [47]. In these instances, if small pits form initially at which chlorides
concentrate (Figs. 19.5 and 19.7) (see Section 19.2.4.1), the cracking tendency is
accentuated by concentrated FeCl2 and analogous metal chlorides within the pits.
Hence, oxygen may induce stress-corrosion cracking in sodium chloride solutions
because pitting occurs when it is present. Another contributing factor is a shift
of the corrosion potential in the presence of oxygen, but not in its absence, to
values that are noble to the critical potential for stress-corrosion cracking. For
this situation, stress-corrosion cracking can occur regardless of whether corrosion
pits develop.
Cracking by alkaline solutions requires relatively high concentrations of
OH−; hence, cracking of 18–8 usually occurs not in alkaline boiler water, but
Figure 19.8. Relation between chloride and oxygen content of boiler water on stress-
corrosion cracking of austenitic 18–8-type stainless steels exposed to steam phase with inter-
mittent wetting; pH 10.6, 50 ppm PO3− 4 , 242–260°C (467–500°F), 1–30 days’ exposure [W.
Williams and J. Eckel, J. Am. Soc. Nav. Eng. 68, 93 (1956)].
rather within the splash zone above the water line where dissolved alkalies con-
centrate by evaporation. Failures can occur in such solutions in the absence of
dissolved oxygen [48]. There is no evidence that transgranular stress-corrosion
cracking occurs in pure water or pure steam.
Cracking of stressed, nickel-free ferritic steels, in general, does not occur in
the chloride media described previously, these steels being sufficiently resistant
to warrant their practical use in preference to austenitic stainless steels in chlo-
ride-containing solutions. They (e.g., type 430) are also resistant to 55% Ca(NO3)2
solution boiling at 117°C and to 25% NaOH solution boiling at 111°C [49]. When
alloyed with more than 1.5% Ni, the 18% Cr–Fe, 0.003% C stainless steels, cold-
rolled, are susceptible to transgranular stress-corrosion cracking in MgCl2 boiling
at 130°C. When annealed at 815°C for 1 h, only the alloy containing 2% Ni fails;
both higher and lower nickel contents resist cracking up to 200 h [50]. The effect
of nickel is partly explained by an observed shift of potentials such that, at and
above 1.5% Ni, the corrosion potential of the cold-rolled material becomes noble
to the critical potential; hence cracking occurs. The reverse order of potentials
applies to alloys of lower nickel content [50].
In slightly or moderately acidic solutions, the martensitic steels, when heat-
treated to high hardness values, are very sensitive to cracking, particularly in the
presence of sulfides, arsenic compounds, or oxidation products of phosphorus or
selenium. The specific anions of the acid make little difference so long as hydro-
gen is evolved, contrary to the situation for austenitic steels, for which only spe-
cific anions are damaging. Also, cathodic polarization, rather than protecting
against cracking, accelerates failure. All these facts suggest that the martensitic
steels under these conditions fail not by stress-corrosion cracking but by hydro-
gen cracking (see Section 8.4). The more ductile ferritic stainless steels undergo
hydrogen blistering instead when they are cathodically polarized in seawater,
especially at high current densities. Austenitic stainless steels are immune to both
hydrogen blistering and cracking.
Galvanic coupling of active metals to martensitic stainless steels may also
lead to failure because of hydrogen liberated on the stainless (cathodic) surface.
Such failures have been demonstrated in laboratory tests [51]. As mentioned in
Section 8.4, practical instances have been noted of self-tapping martensitic
stainless-steel screws cracking spontaneously soon after being attached to an
aluminum roof in a seacoast atmosphere. Similarly, hardened martensitic stain-
less-steel propellers coupled to the steel hull of a ship have failed by cracking
soon after being placed in service. Severely cold-worked 18–8 austenitic stainless
steels may also fail under conditions that would damage the martensitic types
[52]. Here again, sulfides accelerate damage, and since the alloy on cold working
undergoes a phase transformation to ferrite, the observed effect is probably
another example of hydrogen cracking.
Martensitic stainless steels and also the precipitation-hardening types, heat-
treated to approximately >200,000 psi (>1,400 MPa) yield strength, have been
reported to crack spontaneously in the atmosphere, in salt spray, and immersed
in aqueous media, even when not coupled to other metals [53–55]. Martensitic
stainless-steel blades of an air compressor [56] have failed along the leading edges
where residual stresses were high and where condensation of moisture occurred.
Stressed to about 75% of the yield strength, and exposed to a marine atmosphere,
life of ultra-high-strength 12% Cr martensitic stainless steels was in the order of
10 days or less [57]. It is generally accepted that ultra-high strength steels crack
by a hydrogen embrittlement mechanism [55].
19.2.5.1 Metallurgical Factors. Austenitic stainless steels containing more

than about 45% Ni are immune to stress-corrosion cracking in boiling MgCl2
solution and probably in other chloride solutions as well (Fig. 19.9) [58]. Ede-
leanu and Snowden [48] noted that high-nickel stainless steels were more resis-
tant to cracking in alkalies. Increasing the amount of nickel in austenitic stainless
steels shifts the critical potential for stress-corrosion cracking in MgCl2 solution
in the noble direction more rapidly than it shifts the corresponding corrosion
Figure 19.9. Stress-corrosion cracking of 15–26% Cr–Fe–Ni alloy wires in boiling 42% MgCl2.
Low-nickel or nickel-free alloys are ferritic and do not crack. Austenitic alloys do not crack
above 45% Ni [58].
potential; hence, the alloys become more resistant [59]. At and above approxi-
mately 45% Ni, the alloys resist stress-corrosion cracking regardless of applied
potential, indicating that not environmental, but metallurgical factors, such as
unfavorable dislocation arrays or decreasing interstitial nitrogen solubility,
become more important.
For austenitic steels that are resistant to transformation on cold working
(e.g., type 310), nitrogen is the element largely responsible for stress-cracking
susceptibility, whereas additions of carbon decrease susceptibility (Fig. 19.10)
[60]. The effect is related to alloy imperfection structure rather than to any shift
of either critical or corrosion potential [59]. Stabilizing additions effective in
preventing intergranular corrosion, such as titanium or columbium, have no
Figure 19.10. Stress-corrosion cracking of cold-rolled 19% Cr, 20% Ni austenitic stainless
steels in boiling MgCl2 (154 °C) as affected by carbon or nitrogen content [60].
beneficial effect on stress-corrosion cracking, nor do alloying additions such as

2–3% Mo in type 316 stainless steel. Chloride S.C.C. occurs primarily above
about 90°C (190°F), but, in acidified chloride solutions, S.C.C. can occur at lower
temperatures [61, 62].
19.2.6 Cracking of Sensitized Austenitic Alloys

in Polythionic Acids
During shutdown of certain 18–8 stainless-steel oil-refinery equipment operating
in the carbide precipitation temperature range, it was found that rapid inter-
granular cracking occurred in the presence of a tensile stress (but not otherwise).
The cause was traced to polythionic acids (H2SxO6 where x = 3,4,5) formed by
reaction of residual metallic sulfide films on the equipment surface with moist
air at room temperature [63–66]. Such acids can be produced in the laboratory
by bubbling H2S through water saturated with SO2. It is important to the mecha-
nism of failure that these acids are readily reduced cathodically by operating
corrosion cells.
One function of polythionic acids is to act as cathodic depolarizers, thereby
stimulating dissolution of chromium-depleted grain-boundary material. Another
possible function is that their cathodic reduction products (H2S or analogous
compounds) stimulate absorption to interstitial hydrogen by chromium-depleted
alloy. The latter alloy along grain boundaries, ferritic in structure, is subject to
hydrogen cracking when stressed, unlike the grains austenitic in structure that
are resistant. The function of >2 ppm sulfur as Na2S or as cathodic reduction
products of sulfites ( SO2− 2−
3 ) or of thiosulfates ( S 2 O3 ) to induce hydrogen cracking
of a 0.77% C high-strength steel and also of ferritic and martensitic stainless
steels was demonstrated in seawater [67]. It is expected that polythionic acids
would act in an analogous manner.
The mechanism of failure has been described as S.C.C. by electrochemical
dissolution along an active path exposed through application of stress [68]. Alter-
natively, the mechanism may be one of progressive hydrogen cracking along the
grain boundaries of sensitized alloy. An acid environment is necessary to failure
because reaction with alloy supplies the required hydrogen; it also favors forma-
tion of H2S (rather than HS− or S2−), which is the primary catalyst poison stimu-
lating absorption of atomic hydrogen by the alloy. Aqueous SO2 solutions are
also found to cause intergranular cracking of sensitized 18−8, similar to that by
polythionic acids, because SO2− 3 is readily reduced at cathodic sites forming H2S
or similarly acting reduction products, whereas sulfuric acid is much less effective
in causing cracking because SO2− 4 is not similarly reduced.
Cracking in polythionic acids is most pronounced in the potential range
0.04–0.34 V (S.H.E.) [68]. This potential range lies above the values associated
with hydrogen ion discharge and would seem to rule out hydrogen cracking.
However, the relevant potential is not the one measured at the alloy surface, but
the one prevailing at the crack tip, which can be appreciably more active. In
practice, use of stabilized stainless steels avoids intergranular cracking of the kind
described.
To Reduce or Eliminate Cracking

Austenitic Stainless Steels
a. Cathodically protect. The critical potential of 18–8 stainless steel in MgCl2
at 130 °C is −0.128 V (S.H.E.). Coupling of stressed 18–8 to a small area
of nickel (φcorr = −0.18 V) prevents cracking in this medium, or (as a porous
nickel coating) in water containing 50 ppm Cl− at 300°C [69].
b. In acid environments, eliminate Cl−. In neutral or slightly alkaline chloride
environments, eliminate dissolved oxygen and other oxidizing ions. Add
extraneous ions (e.g., NO−3 , I−, acetates).
c. Avoid high concentrations of OH−. High concentrations of alkalies occur-
ring initially or incidentally through concentration at crevices or in vapor
zones are damaging. Add buffering ions (e.g., PO3− 4 ).
d. Use alloys containing >45% Ni or reduce the nitrogen content (and

other detrimental impurities, if present) to the lowest possible value
(<0.04% N in the case of 20% Cr, 20% Ni, 0.001% C stainless steel)
(Fig. 19.10).
e. Substitute ferritic alloys (e.g., type 430 or controlled purity Cr–Mo steels).
However, ferritic alloys may become embrittled by hydrogen or they may
blister when galvanically coupled to more active metals in certain

environments.
f. Operate below 60–80°C (140–175°F).
Martensitic, Precipitation-Hardening, or Ferritic Stainless Steels

a. Avoid excess current if cathodic protection is applied.
b. Avoid galvanic coupling to more active metals.
c. Temper martensitic or precipitation-hardening steels to the lowest possi-
ble hardness values. Exposed to the atmosphere, hardness should be
below about Rockwell C 40. Maximum susceptibility of types 410 and 420
stainless steels to cracking in salt spray or to hydrogen cracking occurs
after tempering for 2 h at 425–550°C (800–1000°F); minimum susceptibil-
ity to hydrogen cracking occurs after tempering for 2 h at 260°C (500°F)
[70].
19.2.7 Galvanic Coupling and General Corrosion Resistance

Since stainless steels are passive and exhibit a noble potential, they can be
coupled successfully to metals that are either passive or inherently noble. This
includes metals and alloys like silver; silver solder; copper; nickel; 70% Ni−Cu
alloy; 76% Ni, 16% Cr, 7% Fe alloy; and, usually, aluminum in environments in
which it remains passive.
As discussed in Section 19.2.4, stainless steels are best employed under fully
aerated or oxidizing conditions, which favor the passive state. Whether used in
handling chemicals or exposed to the atmosphere, the alloy surface should always
be kept clean and free of surface contamination. Otherwise, crevice corrosion
may cause pitting and localized rusting. Austenitic stainless steels cooled too
slowly through the sensitizing temperature zones tend to rust in the
atmosphere.
In brief, stainless steels are resistant to:
1. Nitric acid, over a wide range of concentrations and temperatures.

2. Very dilute sulfuric acid at room temperature when aerated; higher con-
centrations (e.g., 10%) and at boiling temperatures if Fe3+, Cu2+, or nitric
acid is added as an inhibitor [71]; or at lower temperatures if small amounts
of Cu, Pt, or Pd are alloyed (see Section 6.4). Also resistant to cold or hot
sulfuric acid if anodically protected.
3. Many organic acids, including almost all food acids and acetic acid (but
not boiling glacial acetic acid).
−
4. Sulfurous acid (in the absence of SO2− 4 or Cl ).
5. Alkalies, except under stress in hot concentrated caustic solutions.

6. The atmosphere. Types 302 and 304 have been used successfully as archi-
tectural trim of storefronts and buildings (e.g., the Chrysler and Empire
State buildings in New York City). These and type 430 are used for auto
trim.
Stainless steels are not resistant to:
1. Dilute or concentrated HCl, HBr, and HF; also not resistant to salts that
hydrolyze to these acids.
2. Oxidizing chlorides (e.g., FeCl3, HgCl2, CuCl2, and NaOCl).
3. Seawater, except for brief periods or when cathodically protected.
4. Photographic solutions, especially fixing solutions containing thiosulfates
(pitting occurs).
5. Some organic acids, including oxalic, formic, and lactic acids.
6. Stressed austenitic alloys (e.g., type 304) in waters containing Cl− plus O2
at temperatures above 60–80°C.
REFERENCES
1. G. Tammann, Lehrbuch der Metallkunde, Leipzig, 1932, pp. 428–433.

2. H. Pickering and C. Wagner, J. Electrochem. Soc. 114, 698 (1967); H. Pickering, J. Elec-
trochem. Soc. 115, 143 (1968).
3. W. Katz, in Korrosion und Korrosionsschutz, F. Tödt, editors, de Gruyter, Berlin,
1955, pp. 412–414.
4. J. J. Noël, Effects of metallurgical variables on aqueous corrosion, in ASM Handbook,
Vol. 13A, Corrosion: Fundamentals, Testing, and Protection, ASM International,
5. J. R. Scully and A. Lucente, Corrosion of amorphous metals, in ASM Handbook,
Vol. 13B, Corrosion: Materials, ASM International, Materials Park, OH, 2005, pp.
476–489.
6. J. Stodart and M. Faraday, Q. J. Sci. Lit. Arts 9, 319 (1820); Philos. Trans. Roy. Soc.
112, 253 (1822).
7. P. Berthier, Ann. Chim. Phys. 17, 55 (1821); Ann. Mines 6, 573 (1821).
8. L. Guillet, Rev. Met. 1, 155 (1904); 2, 350 (1905); 3, 332 (1906).
9. P. Monnartz, Metallurgie 8, 161 (1911).
10. M. L. Erbing Falkland, Duplex stainless steels, in Uhlig’s Corrosion Handbook, 2nd
11. J. F. Grubb, T. DeBold, and J. D. Fritz, Corrosion of wrought stainless steels, in ASM
Handbook, Vol. 13B, Corrosion: Materials, ASM International, Materials Park, OH,
2005, pp. 56–57.
12. R. Steigerwald, A. Bond, H. Dundas, and E. Lizlovs, Corrosion 33, 279 (1977).
13. J. Truman, R. Perry, and G. Chapman, J. Iron Steel Inst. 202, 745 (1964).
REFERENCES 363
14. H. H. Uhlig, Trans. Am. Soc. Metals 30, 947 (1942).

15. J. Upp, F. Beck, and M. Fontana, Trans. Am. Soc. Metals 50, 759 (1958).
16. W. Binder, C. Brown, and R. Franks, Trans. Am. Soc. Metals 41, 1301 (1949).
17. H. Ebling and M. Scheil, in Advances In Technology of Stainless Steels and Related
Alloys, American Society for Testing And Materials, Philadelphia, 1965, p. 275.
18. E. Bain, R. Aborn, and J. Rutherford, Trans. Am. Soc. Metals (Steel Treating) 21, 481
(1933); B. Strauss, H. Schottky, and J. Hinnüber, Z. Anorg. Allgem. Chem. 188, 309
(1930). See also M. A. Streicher, Austenitic and ferritic stainless steels, in Uhlig’s
Corrosion Handbook, 2nd edition, R. W. Revie, editor, Wiley, New York, 2000,
p. 613.
19. H. H. Uhlig, Trans. Electrochem. Soc. 87, 193 (1945). See also Ref. 16.
20. P. Schafmeister, Arch. Eisenhüttenw. 10, 405 (1936–37).
21. P. Lacombe, in Proceedings of the First International Congress on Metallic Corrosion,
Butterworths, London, 1962; A. Baümel et al., Corros. Sci. 4, 89 (1964), pp. 21–35.
22. M. A. Streicher, Austenitic and ferritic stainless steels, in Uhlig’s Corrosion Handbook,
2nd edition, R. W. Revie, editor, Wiley, New York, 2000, p. 613.
23. Ref. 22, p. 615.
24. M. Streicher, J. Electrochem. Soc. 106, 161 (1959).
25. H. Coriou et al., Corrosion 22, 280 (1966).
26. J. Armijo, Corros. Sci. 7, 143 (1967).
27. J. Armijo, Corrosion 24, 24 (1968).
28. Y. Kolotyrkin and O. Kasparova, in Corrosion and Corrosion Protection, R.
Frankenthal and F. Mansfeld, editors, Electrochemical Society, Pennington, NJ, 1981,
p. 186.
29. J. Wanklyn and D. Jones, J. Nucl. Mater. 2, 154 (1959).
30. H. Copson and G. Economy, Corrosion 24, 55 (1968).
31. H. Coriou et al., in Fundamental Aspects of Stress Corrosion Cracking, National Asso-
ciation of Corrosion Engineers, Houston, TX, 1969, pp. 352–359.
32. W. Hübner, M. de Pourbaix, and G. Östberg, in Proceedings of the Fourth International
Congress on Metallic Corrosion, Amsterdam, September 1969, National Association
33. R. Duncan, J. Armijo, and A. Pickett, Mater. Prot. 8, 37 (1969).
34. R. Lula, A. Lena, and G. Kiefer, Trans. Am. Soc. Metals 46, 197 (1954).
35. E. Houdremont and W. Tofaute, Stahl Eisen 72, 539 (1952).
36. J. Hochmann, Rev. Met. 48, 734 (1951).
37. A. Bond and E. Lizlovs, J. Electrochem. Soc. 116, 1305 (1969).
38. A. Bäumel, Stahl Eisen 84, 798 (1964).
39. R. Frankenthal and H. Pickering, J. Electrochem. Soc. 120, 23 (1973).
40. J. Matthews and H. Uhlig, Corrosion 7, 419 (1951).
41. P. Schafmeister and W. Tofaute, Tech. Mitt. Krupp 3, 223 (1935).
42. P.-E. Arnvig and A. D. Bisgård, Paper 437, CORROSION/96, NACE, Houston, Texas,
1996; P. Ernst and R. C. Newman, Corrosion Sci. 49(9), 3705 (2007).
43. H. H. Uhlig, Trans. Am. Inst. Min. Metall. Eng. 140, 411 (1940).
44. F. L. LaQue, in Corrosion Handbook, H. H. Uhlig, editor, Wiley, New York, 1948, p.
416.
45. T. Lee and A. Tuthill, Mater. Perf. 22(1), 48 (1983).
46. P. Elliott, in ASM Handbook, Vol. 13A, Corrosion: Fundamentals, Testing, and Protec-
tion, ASM International, Materials Park, OH, 2003, p. 915; W. Williams and J. Eckel,
J. Am. Soc. Nav. Eng. 68, 93 (February 1956).
47. A. Dana, Jr., Am. Soc. Testing Mater. Bull. 225, 46 (1957).
48. C. Edeleanu and P. Snowden, J. Iron Steel Inst. 186, 406 (1957).
49. A. Bond, J. Marshall, and H. Dundas, in Stress Corrosion Testing, Special Technology
Publication No. 425, American Society for Testing and Masterials, Philiadelphia, 1967,
p. 116.
50. R. Newberg and H. Uhlig, J. Electrochem. Soc. 119, 981 (1972).
51. H. H. Uhlig, Metal Progr. 57, 486 (1950).
52. F. Bloom, Corrosion 11, 351t (1955).
53. E. Phelps and R. Mears, First International COngres On Metallic Corrosion, Butter-
worths, London, 1962, p. 319.
54. J. Truman, R. Berry, and G. Chapman, J. Iron Steel Inst. 202, 745 (1964).
55. B. Craig, in ASM Handbook, Vol. 13A, Corrosion: Fundamentals, Testing, and Protec-
tion, ASM International, Materials Park, OH, 2003, p. 373.
56. W. Badger, Soc. Automot. Eng. Trans. 62, 307 (1954).
57. E. Phelps, in Fundamental Aspects of Stress Corrosion Cracking, National Association
58. H. Copson, in Physical Metallurgy of Stress Corrosion Fracture, T. Rhodin, editor,
Interscience, New York, 1959, p. 247.
59. H. Lee and H. Uhlig, J. Electrochem. Soc. 117, 18 (1970).
60. H. Uhlig and J. Sava, quoted in Fracture, Vol. 3, H. Liebowitz, editor, Academic Press,
New York, 1971, p. 656.
61. B. Phull, Evaluating stress-corrosion cracking, in ASM Handbook, Vol. 13A, Corro-
sion: Fundamentals, Testing, and Protection, ASM International, Materials Park, OH,
2003, p. 604.
62. J. D. Harston and J. C. Scully, Corrosion 25, 493 (1969).
63. C. Samans, Corrosion 20, 256t (1964).
64. G. Cragnolino and D. Macdonald, Corrosion 38, 406 (1982).
65. H. Nishida, K. Nakamura, and H. Takahashi, Mater. Perf. 23(4), 38 (1984).
66. R. D. Kane, Corrosion in petroleum refining and petrochemical operations, in ASM
Materials Park, OH, 2006, pp. 991–992.
67. H. Uhlig, Mater. Perf. 16(1), 22 (1977).
68. I. Matsushima, in Proceedings of the Sixth International Congress on Metallic Corro-
sion, Sydney, Australia, 1975, Australasian Corrosion Association, Melbourne,
Australia, p. 514.
69. P. Neumann and J. Griess, Corrosion 19, 345t (1963).
70. P. Lillys and A. Nehrenberg, Trans. Am. Soc. Metals 48, 327 (1956).
71. J. Cobb and H. Uhlig, J. Electrochem. Soc. 99, 13 (1952).
GENERAL REFERENCES
B. D. Craig, Fundamental Aspects of Corrosion Films in Corrosion Science, Plenum Press,

New York, 1991.
Glassy Alloys
J. R. Scully and A. Lucente, Corrosion of amorphous metals, in ASM Handbook, Vol. 13B,
Corrosion: Materials, ASM International, Materials Park, OH, 2005.
Stainless Steels
M. Blair, Corrosion of cast stainless steels, ASM Handbook, Vol. 13B, Corrosion: Materials,
M. L. Erbing Falkland, Duplex stainless steels, in Uhlig’s Corrosion Handbook, 2nd edition,
J. F. Grubb, Martensitic stainless steels, in Uhlig’s Corrosion Handbook, 2nd edition,
J. F. Grubb, T. DeBold, and J. D. Fritz, Corrosion of wrought stainless steels, in ASM Hand-
book, Vol. 13B, Corrosion: Materials, ASM International, Materials Park, OH, 2005, pp.
54–77.
H. S. Khatak and B. Raj, editors, Corrosion of Austenitic Stainless Steels: Mechanism, Mitiga-
tion and Monitoring, Narosa Publishing House, New Delhi, 2002.
A. J. Sedriks, Corrosion of Stainless Steels, 2nd edition, Wiley, New York, 1996.
M. A. Streicher, Austenitic and ferritic stainless steels, in Uhlig’s Corrosion Handbook, 2nd
20
COPPER AND COPPER ALLOYS
20.1 COPPER
Cu 2 + + 2e − → Cu φ° = 0.337 V
Copper dissolves anodically in most aqueous environments forming the divalent

ion Cu2+. Equilibrium relations at the metal surface indicate that the reaction Cu
+ Cu2+ W 2Cu+ is displaced far to the left (see Problem 1, p. 381). On the other
hand, if complexes are formed, as, for example, between Cu+ and Cl− in a chloride
solution, the continuous depletion of Cu+ by conversion to CuCl −2 favors the
univalent ion as the major dissolution product. Comparatively, when copper is
heated in air at elevated temperatures, a Cu2O film develops that is covered by
a thin film of CuO, which is formed as the film thickness increases [1].
In Fig. 20.1, the theoretical potential–pH domains of corrosion, immunity,
and passivation of copper at 25°C are shown, considering that passivation occurs
by formation of the oxides Cu2O and CuO [2].
Copper and its alloys, although toxic to fouling organisms, such as seaweed
and shellfish, are subject to microbiologically influenced corrosion, undergoing
severe attack by sulfide if conditions allow the growth of sulfate reducing bacteria
[3, 4].

367
368 COPPER AND COPPER ALLOYS
Figure 20.1. Theoretical potential–pH domains of corrosion, immunity, and passivation for
copper, assuming that passivation results from the formation of the oxides, Cu2O and CuO
[2]. (M. Pourbaix, Atlas of Electrochemical Equilibria in Aqueous Solutions, 2nd English edition,
p. 389. Copyright NACE International 1974 and CEBELCOR.)
Figure 20.2. Longitudinal cross section of undercut pits associated with impingement attack
of condenser alloy by salt water (7×) (flow of water from left to right).
Copper is a metal widely used because of good corrosion resistance com-

bined with mechanical workability, excellent electrical and thermal conductivity,
and ease of soldering or brazing. It is noble to hydrogen in the Emf Series, and
it is thermodynamically inert with no tendency to corrode in water and in non-
oxidizing acids free of dissolved oxygen. In oxidizing acids and in aerated solu-
tions of ions that form copper complexes (e.g., CN−, NH +4 ), corrosion can be
severe. Copper is also characterized by sensitivity to corrosion by high-velocity
water and by aqueous solutions, called impingement attack (Fig. 20.2). The rate
increases with dissolved oxygen content, whereas in air-free high-velocity water
COPPER 369
up to at least 7.5 m/s (25 ft/s), impingement attack is negligible. In groundwaters,

the corrosion rate increases with increasing salinity (concentration of dissolved
salts) [5]. The rate of corrosion increases with dissolved oxygen concentration
and temperature. In an open system, the rate of corrosion may show a maximum
as temperature is increased because the solubility of oxygen decreases with tem-
perature [5].
20.1.1 Corrosion in Natural Waters

Copper is resistant to seawater, with the corrosion rate in temperate climates
being about 0.5–1.0 gmd (0.001–0.002 ipy) in quiet water and somewhat higher in
moving water. In tropical climates, the rate increases by 11/2–2 times. It is one
of the very few metals that remains free of fouling organisms, with normal cor-
rosion being sufficient to release copper ions in concentrations that poison marine
life.
In seawater and in fresh waters, corrosion resistance depends on the presence
of a surface oxide film through which oxygen must diffuse in order for corrosion
to continue. Upon exposure to distilled water at room temperature, the oxide
film on copper is found to be a mixture of Cu2O and CuO [6, 7]. Visible light
markedly retards the rate of oxide formation [6]. The film is easily disturbed by
high-velocity water or is dissolved by either carbonic acid or the organic acids
that are found in some fresh waters and soils, leading to a high corrosion rate.
For example, a hot water in Michigan, zeolite softened with resultant high con-
centration of NaHCO3, perforated copper water pipe within 6–30 months [8]. The
same water unsoftened, on the other hand, was not nearly as corrosive because
a protective film of CaCO3 containing some silicate was deposited on the metal
surface. Copper piping used to transport well water in homes in some areas of
New Jersey [9] developed pinhole leaks (pits) within 10 years.
Even if the corrosion rate is not excessive and the copper is durable, a water
containing carbonic or other acids nevertheless may corrode copper and copper-
base alloys sufficiently to cause blue staining of bathroom fixtures and cause an
increase in the corrosion rate of iron, galvanized steel, or aluminum surfaces with
which such water comes into contact. Accelerated corrosion in this instance is
caused by a replacement reaction in which copper metal is deposited on the base
metal, forming numerous small galvanic cells. Treatment of acid waters or waters
of negative saturation index with lime or with sodium silicate reduces the corro-
sion rate sufficiently to overcome both staining and accelerated corrosion of
other metals, except aluminum. Aluminum is an exception because of its sensitiv-
ity to extremely small amounts of Cu2+ in solution, with the usual water treatment
being inadequate to reduce Cu2+ pickup to nondamaging levels. The U.S. Envi-
ronmental Protection Agency Lead and Copper Rule, implemented in 1991,
limits total copper in potable water to a maximum of 1.3 mg L−1 [10].
It is possible to avoid the damaging effects of Cu2+ contamination of water
by using copper piping coated on the inside surface with tin (tinned copper). For
this reason, copper tanks for holding distilled water or for water storage on ships
should be tinned [11]. The tin coating must be pore free in order to avoid acceler-
ated attack of copper at exposed areas, since tin (or copper–tin intermetallic
compounds) is cathodic to copper.
Copper piping is usually satisfactory for transporting seawater and hard
waters, whether hot or cold. Hard waters form a protective film of calcium com-
pounds on the copper surface that protects against corrosion. In soft waters,
particularly those containing appreciable amounts of free carbon dioxide, and in
carbonated waters in general, the corrosion rate of copper is significant. The
initial corrosion rate in distilled water may be 0.051–0.16 mm/year (12–7 mdd),
whereas the rate in an aggressive supply water, as high as 0.26 mm/year (62 mdd),
may result in sufficient copper to stain plumbing fixtures [11].
In addition to the effects just described, a pitting type of corrosion may be
induced in waters having relatively good conductivity if dirt or rust from other
parts of the system accumulate on the copper surface. Differential aeration cells
are formed, supplemented in some cases by turbulent flow, which initiates
impingement attack. The resulting corrosion is sometimes called deposit attack.
Periodic cleaning of the piping or tubing usually prevents corrosion by such
deposits.
Even when the copper surface is free of deposits, pitting nevertheless may
occur in waters of certain compositions or as a result of pipe fabrication methods.
In this respect, the types of pits that can develop on copper have been divided
into categories [12, 13]. The first category, type 1 pitting, usually takes place in
hard or moderately hard waters and is usually restricted to the cold portions of
the system. Pits of this type contain a higher proportion of cuprous chloride than
do pits formed in soft water, and mounds consist largely of cupric carbonate. The
surrounding surface scale is largely CaCO3 stained green, beneath which is a
highly cathodic film of carbon [14] that was the residue of the lubricant used
during pipe manufacture. Type 1 pitting has been largely eliminated by improve-
ments in the tube manufacturing processes [11].
In the second category are soft waters containing small amounts of manga-
nese salts. With these waters, pitting, designated as Type 2 pitting, usually occurs
in the hottest part of the system, above 60°C, in waters with low bicarbonate/
sulfate ratio, < 1. In this case, corrosion products within the pit are Cu2O plus a
small amount of chloride, whereas mounds around the pits may contain basic
copper sulfate, and the pipe surface is covered by a black scale rich in manganese
oxide.
To protect copper hot-water tanks from pitting, sacrificial anodes of alumi-
num are sometimes used, particularly in certain areas of Great Britain [15].
In summary, copper is resistant to:
1. Seawater.
2. Fresh waters, hot or cold. Copper is especially suited to convey soft,
aerated waters that are low in carbonic and other acids.
3. Deaerated, hot or cold, dilute H2SO4, H3PO4, acetic acid, and other non-
oxidizing acids.
COPPER ALLOYS 371
4. Atmospheric exposure.
5. Halogens under specific conditions—for example, fluorine below about
400°C, dry HF below 600°C, dry Cl2 below 150°C, dry Br2 at 25°C, iodine
below 375°C [16].
Copper is not resistant to:
1. Oxidizing acids, for example, HNO3, hot concentrated H2SO4, and aerated
nonoxidizing acids (including carbonic acid).
2. NH4OH (plus O2). A complex ion, Cu(NH 3)2+ 4 , forms. Substituted NH3
compounds (amines) are also corrosive. These compounds are those that
cause stress-corrosion cracking of susceptible copper alloys.
3. High-velocity aerated waters and aqueous solutions. In corrosive waters
(high in O2 and CO2, low in Ca2+ and Mg2+), the velocity should be kept
[8, 13] below 1.2 m/s (4 ft/s); in less corrosive waters, <65°C (<150°F), the
velocity should be kept below 2.4 m/s (8 ft/s).
4. Oxidizing heavy metal salts, for example, FeCl3 and Fe2(SO4)3.
5. Hydrogen sulfide, sulfur, and some sulfur compounds.
20.2 COPPER ALLOYS
Tin bronzes are copper–tin alloys noted for their high strength. Alloys containing
more than 5% Sn are especially resistant to impingement attack. The copper–
silicon alloys containing 1.5–4% Si have better physical properties than copper
and similar general corrosion resistance. Seawater immersion tests at Panama
showed that 5% Al−Cu was the most resistant of the common copper-base alloys,
losing only 20% of the corresponding weight loss of copper after 16 years [17].
20.2.1 Copper–Zinc Alloys (Brasses)

Copper–zinc alloys have better physical properties than copper alone, and they
are also more resistant to impingement attack; hence, brasses are used in prefer-
ence to copper for condenser tubes. Corrosion failures of brasses usually occur
by dezincification, pitting, or stress-corrosion cracking. The tendency for brass to
corrode in these ways, except for pitting attack, varies with zinc content, as shown
in Fig. 20.3. Pitting is usually caused by differential aeration cells or high-velocity
conditions. It can normally be avoided by keeping the brass surface clean at all
times and by avoiding velocities and design geometry that lead to impingement
attack.
Various names have become attached to brasses of different zinc content.
Muntz metal, 40% Zn−Cu, is used primarily for condenser systems that use fresh
water (e.g., Great Lakes water) as coolant. Naval brass is a similar composition,
but containing 1% Sn. Manganese bronze is also similar, containing about 1%
Figure 20.3. Trends of dezincification, stress-corrosion cracking, and impingement attack

with increasing zinc content in copper–zinc alloys (brasses).
each of tin, iron, and lead; it is used for ship propellers, among other applications.
Dezincification of manganese bronze propellers in seawater is avoided to some
extent by the cathodic protection afforded by the steel hull.
Yellow brass, 30% Zn−Cu, is used for a variety of applications where easy
machining and casting are desirable. The alloy gradually dezincifies in seawater
and in soft fresh waters. This tendency is retarded by addition of 1% Sn, the cor-
responding alloy being called admiralty metal or admiralty brass. Addition of
small amounts of arsenic, antimony, or phosphorus still further retards the rate
of dezincification; the resulting alloy, called inhibited admiralty metal, is used in
seawater or fresh-water condensers.
Red brass, 15% Zn−Cu, is relatively immune to dezincification, but is more
susceptible to impingement attack than yellow brass.
20.2.2 Dealloying/Dezincification
Dezincification, as one type of dealloying, was defined in Section 2.4. Other
types of dealloying include the selective dissolution of copper in copper–gold
alloys.
In brasses, dezincification takes place either in localized areas on the metal
surface, called plug type (Fig. 20.4), or uniformly over the surface, called layer
type (Fig. 20.5). Brass so corroded retains some strength, but has no ductility.
Layer-type dezincification in a water pipe may lead to splitting open of the pipe
under conditions of sudden pressure increase; and, for plug type, a plug of dez-
incified alloy may blow out, leaving a hole. Because dezincified areas are porous,
COPPER ALLOYS 373
Figure 20.4. Plug-type dezincification in brass pipe (actual size).
Figure 20.5. Layer-type dezincification in brass bolts (actual size).

plugs may be covered on the outside surface with corrosion products and residues
of evaporated water.
Conditions of the environment that favor dezincification are (1) high tem-
peratures, (2) stagnant solutions, especially if acid, and (3) porous inorganic scale
formation. Looking at the situation metallurgically, brasses that contain 15% or
less zinc are usually immune. Also, dezincification of α-brasses (up to 40% Zn)
can be reduced, as mentioned earlier, by small alloying additions of tin plus a few
hundredths percent arsenic, antimony, or phosphorus.
Although inhibited admiralty brass resists dezincification, conditions favor-
ing thermogalvanic action between overheated local areas and adjoining colder
areas of heat exchanger tubes can cause attack of this kind at the overheated
zones. Attack is reduced by using inhibited or scaling (positive saturation index)
waters [18].
The detailed mechanisms of dealloying have recently been reviewed [19]. The
four main mechanisms that researchers have developed to account for the pro-
cesses by which one metal in an alloy is removed by corrosion, leaving behind a
porous metal, are:
1. The ionization–redeposition mechanism, according to which the alloy cor-

rodes and the more noble metal (copper in copper–zinc alloys) is then
redeposited to form a porous outer layer [20].
2. The volume diffusion mechanism, based on selective dissolution of the less
noble element and volume diffusion of both elements in the solid phase
[21, 22].
3. The surface diffusion mechanism, in which only the less noble element
(zinc in copper–zinc alloys) dissolves and the remaining more noble metal
is rearranged by diffusion on the surface and nucleation of islands of
almost pure metal [23].
4. The percolation model of selective dissolution, an extension of the surface
diffusion mechanism, based on preexisting interconnected paths of like
elements in the binary alloy and effects of curvature on dissolution poten-
tial [24, 25].
Any one of these mechanisms may apply in specific instances of dealloying. For
example, twin bands in brass, visible in the completely or incompletely dezincified
layer, constituted early evidence for a volume diffusion mechanism of zinc trans-
port from the bulk alloy to the surface [26]. In the gold–copper alloy system,
copper corrodes preferentially, without dissolution of gold, leaving a porous
residue of gold–copper alloy or pure gold.
20.2.3 Stress-Corrosion Cracking (Season Cracking)

Virtually all copper alloys, as well as pure copper, can be made to crack in
ammonia [27]. Requirements for cracking include the presence of water, ammonia,
COPPER ALLOYS 375
air or oxygen, and tensile stress in the metal. Only trace amounts of ammonia
are required in many cases, and cracking occurs at ambient temperature. Stress-
corrosion cracking failures of copper pipe under elastomeric insulation have been
attributed to wet ammoniacal environments [27, 28]. Small concentrations of
hydrogen sulfide inhibit S.C.C. of brass in petroleum refinery process streams,
most likely by reducing the dissolved oxygen concentration [27, 29].
When an α brass is subjected to an applied or residual tensional stress in
contact with a trace of NH3 or a substituted ammonia (amine), in the presence
of oxygen (or another depolarizer) and moisture, it cracks usually along the grain
boundaries (intergranular) (see Fig. 20.6). Cracking through the grains (trans-
granular) may occur in specific test solutions or if the alloy is severely deformed
plastically.
According to one source, both types of cracking were originally called season
cracking because of the resemblance of stress-corrosion cracks in bar stock to
those of seasoned wood. In England, the origin of the term is ascribed to the fact
that years ago brass cartridge cases stored in India were observed to crack, par-
ticularly during the monsoon season.
Traces of nitrogen oxides may also cause stress-corrosion cracking, probably
because such oxides are converted to ammonium salts on the brass surface by
chemical reaction with the metal. In one instance of this kind, premature failure
of yellow brass brackets in the humidifier chamber of an air-conditioning system
was traced to this cause [30]. The air had passed through an electrostatic dust
Figure 20.6. Intergranular stress-corrosion cracking of brass (75×) (specimen stored 1 year).
precipitator, the high voltage field of which generated traces of nitrogen oxides.
These, in turn, formed corrosion products on the brass surface which were found
by analysis to contain a high proportion of NH4, causing intergranular cracking
of the stressed brackets. Similar cracking of stressed brass could be reproduced
in the laboratory over a period of days by using a spark discharge in air of 100%
relative humidity.
Stress-corrosion cracking of 12% Ni, 23% Zn−Cu alloy (nickel brass) parts
of Central Office Telephone Equipment in Los Angeles occurred within two
years for similar reasons [31]. Pollution of Los Angeles air accounts for abnor-
mally high concentrations of nitrogen oxides and suspended nitrates, with the
latter settling down as dust on the brass parts. Similar failures have not been
observed as frequently in New York City, where the air contains less nitrate, but
also many more sulfate particles than Los Angeles air, indicating that sulfates
may act as inhibitors.
Mattsson [32] observed that minimum cracking time of 37% Zn−Cu brass in
a solution of 1 mole NH 3 + NH +4 , plus 0.05 mole CuSO4 per liter occurred at pH
7.3, with times to failure being longer at higher pH and considerably longer at
lower pH values. Johnson and Leja [33] reported stress-corrosion cracking of
brass in alkaline cupric citrate and in tartrate solutions at pH values in which
complexing of Cu2+ is pronounced.
Figure 20.7 shows the effect of applied potential [34] on S.C.C. of 37% Zn−Cu
brass in a solution similar to that proposed by Mattsson. The critical potential
below which cracking does not occur is 0.095 V (S.H.E.). Since the corresponding
corrosion potential is 0.26 V, S.C.C. on simple immersion of brass is spontaneous.
Stress-corrosion cracking also occurs on substituting Cd2+ or Co2+ in place of Cu2+
additions, but at more noble potentials. It is found that, in the absence of other
metal ammonium complexes, the equivalent of more than 0.003M Cu2+ must be
present in the test solution for spontaneous cracking to occur. Also, addition of
more than 0.005M NaBr or 0.04M NaCl to the Mattsson test solution inhibits
spontaneous cracking. The latter observations are related to a shift of potentials
by Cu2+, Br−, or Cl− such that, when cracking does not occur, the corrosion poten-
tial in each case lies active to the critical potential for S.C.C.
Annealed brass, if not subject to a high applied stress, does not stress-corro-
sion crack. Whether residual stresses in cold-worked brass are sufficient to cause
stress-corrosion cracking in an ammonia atmosphere can be checked by immers-
ing brass in an aqueous solution of 100 g mercurous nitrate [Hg2(NO3)2] and
13 mL nitric acid (HNO3, specific gravity 1.42) per liter of water. Mercury is
released and penetrates the grain boundaries of the stressed alloy. If cracks do
not appear with 15 min, the alloy is probably free of damaging stresses.
No alloying additions in small amounts effectively provide immunity to this
type of failure in brasses. Low-zinc brasses are more resistant than high-zinc
brasses.
High-zinc brasses (e.g., 45–50% Zn−Cu) having a β or β + γ structure, stress-
corrosion crack through the grains (i.e., transgranularly); and, unlike α brasses,
only moisture is required to cause failure [35].
COPPER ALLOYS 377
Figure 20.7. Effect of applied potential on time to failure of 37% Zn−Cu brass in 0.05M
CuSO4, CdSO4, or CoSO4, 1M (NH4)2SO4, pH 6.5 at room temperature [34]. (Reproduced with
The mechanism of stress-corrosion cracking in brasses has been the subject

of much study. Both high-purity alloys and single crystals of α brass crack when
stressed in NH3 atmospheres [36]. In support of an electrochemical mechanism,
it has been noted that the grain boundaries of polycrystalline brasses are more
active in potential than the grains, as measured in NH4OH, but not in FeCl3 solu-
tion, in which stress-corrosion cracking does not occur [37]. It has been proposed,
alternatively, that a brittle oxide film forms on brasses that continuously fractures
under stress exposing fresh metal underneath to further oxidation [38]. Accord-
ing to the generally accepted film rupture mechanism, S.C.C. initiates by film
rupture as a result of plastic deformation at the crack tip. The crack propagates
by localized anodic dissolution, and repassivation is inhibited by further plastic
deformation at the crack tip [39–41].
There is evidence, in any event, that zinc atoms aided by plastic deformation
segregate preferentially at grain boundaries. The resulting composition gradient
favors galvanic action between such areas and the grains, accounting for slow
intergranular attack in a variety of corrosive media without the necessity of an

applied stress (intergranular corrosion). But such areas, subject to plastic defor-
mation, may also favor adsorption of complex ammonium ions within a specific
potential range, leading to rapid crack formation. Similar effects can occur along
slip bands (transgranular cracking). Although segregated zinc may be essential
to the observed intergranular corrosion of brasses, it is probable that the defect
structure of grain boundaries or of slip bands is more important to stress-
corrosion cracking. Hence, failure of copper-base alloys by cracking can occur
when copper is alloyed not only with zinc, but also with a variety of other ele-
ments, such as silicon, nickel, antimony, arsenic, aluminum, phosphorus [42], or
beryllium [43].
To explain the mechanism of transgranular S.C.C. in α brass, Newman and
Sieradzki have proposed the film-induced cleavage model, according to which a
brittle crack that initiates in a thin surface film propagates into the ductile matrix
and eventually blunts and arrests, after which the process repeats itself [39, 44,
45].
Susceptibility to stress-corrosion cracking of brasses can be minimized or
avoided by four main procedures:
1. Stress-Relief Heat Treatment. For 30% Zn−Cu brass, heating at 350°C

(660°F) for 1 h may be effective, but recrystallization and some loss of
strength of the alloy result. Because ammoniacal S.C.C. can occur at rela-
tively low stress levels, stress relief may not be adequate in all cases [27].
2. Avoiding Contact with NH3 (or with O2 and Other Depolarizers in the
Presence of NH3). It is difficult to guarantee that there will be no contact
with NH3, because of the small traces of ammonia that cause cracking.
Plastics containing or decomposing to traces of amines are a continuing
source of damage to unannealed brass. Fertilizer washing from farm land,
or air over fertilized soil, has similarly caused cracking of brass. On the
other hand, brass condenser tubes do not crack in boiler-water condensate
containing NH3, because the concentration of oxygen is extremely low.
3. Cathodic Protection. Cathodic protection to a potential below the critical
value can be provided by either impressed current, or by coating brass
with a sacrificial metal (e.g., zinc).
4. Using H2S as an Inhibitor [27, 29]. The mechanism may, in part, involve
reaction with available free oxygen.
20.2.4 Condenser Tube Alloys Including Copper–Nickel Alloys

For fresh waters, copper, Muntz metal, and admiralty metal (inhibited) are fre-
quently used. For brackish or seawater, admiralty metal, one of the cupro-nickel
alloys (10–30% Ni, bal. Cu) and aluminum brass (22% Zn, 76% Cu, 2% Al, 0.04%
As) are used. For polluted waters, cupro-nickel alloys are preferred over alumi-
num brass because the latter is subject to pitting attack. Aluminum brass may
also pit readily in unpolluted, but stagnant, seawater.
REFERENCES 379
Aluminum brass resists high-velocity waters (impingement attack) better

than does admiralty metal. Cupro-nickel alloys are especially resistant to high-
velocity seawater when they contain small amounts of iron and sometimes man-
ganese as well. For the 10% Ni cupro-nickel alloy, the optimum iron content is
about 1.0–1.75%, with 0.75% Mn maximum; for the analogous 30% Ni composi-
tion, the amount of alloyed iron is usually less (e.g., 0.40–0.70% Fe accompanied
by 1.0% Mn maximum) [46]. It is found that supplementary protective films are
formed on condenser tube surfaces when iron is contained in water as a result
of corrosion products upstream or when added intentionally as ferrous salts.
Accordingly, the beneficial effect of iron alloyed with copper–nickel alloys is
considered to result from similar availability of iron in the formation of protective
films.
The susceptibility of Cu−Ni alloys to corrosion increases in aerated sulfide-
polluted seawater. It appears that sulfides interfere with formation of the usual
protective oxide films [47].
It is pertinent that the 30% Ni−Cu alloy is relatively resistant to stress-cor-
rosion cracking compared to the 10 or 20% Ni−Cu alloys [42], or compared to
any of the 30% Zn−Cu brasses. A detailed general account of the behavior of
copper–nickel alloys, especially the 10% Ni−Cu alloy, in seawater is given by
Stewart and LaQue [48].
REFERENCES
1. C. A. C. Sequeira, Corrosion of copper and copper alloys, in Uhlig’s Corrosion Hand-

book, 2nd edition, R. W. Revie, editor, Wiley, New York, 2000, p. 755.
2. M. Pourbaix, Atlas of Electrochemical Equilibria in Aqueous Solutions, second English
edition, National Association of Corrosion Engineers, Houston, TX, p. 389; and
CEBELCOR, Brussels, 1974.
3. Ref. 1, pp. 750–753, Wiley, New York, 2000.
4. J. F. D. Stott, Evaluating microbiologically influenced corrosion, in ASM Handbook,
Vol. 13A, Corrosion: Fundamentals, Testing, and Protection, ASM International, Mate-
rials Park, OH, 2003, p. 645.
5. A. Cohen, Corrosion of copper and copper alloys, in ASM Handbook, Vol. 13B,
Corrosion: Materials, ASM International, Materials Park, OH, 2005, p. 137.
6. J. Krger, J. Electrochem. Soc. 106, 847 (1959).
7. C. Shanley, R. Hummel, and E. Verink, Corros. Sci. 20, 481 (1980).
8. M. Obrecht and L. Quill, Heating, Piping and Air-Conditioning, January, pp. 165–169;
March, pp. 109–116; April, pp. 131–137; May, pp. 105–113; July, pp. 115–122; September,
pp. 125–133 (1960); April, pp. 129–134 (1961). Also see M. Obrecht, Corrosion 18, 189t
(1962).
9. C. Pfeiffer, Mental and Elemental Nutrients, Keats Publications, New Canaan, CT, 1975,
p. 330.
10. B. J. Little and J. S. Lee, Microbiologically Influenced Corrosion, Wiley, New York, 2007,
p. 184.
11. Ref. 1, p. 747.

12. H. Campbell, J. Appl. Chem. 4, 633 (1954).
13. E. Mattsson, Br. Corros. J. 15, 6 (1980).
14. H. Campbell, J. Inst. Metals 77, 345 (1950).
15. U. R. Evans, An Introduction to Metallic Corrosion, 3rd edition. Arnold, London, 1981,
p. 49.
16. P. Daniel and R. Rapp, Advances in Corrosion Science and Technology, Vol. 5, M.
Fontana and R. Staehle, editor, Plenum Press, New York, 1976, p. 114.
17. C. Southwell, C. Hummer, Jr., and A. Alexander, Mater. Prot. 7, 41 (1968); Mater. Prot.
7, 61 (1968).
18. V. Ereneta, Corros. Sci. 19, 507 (1979).
19. S. G. Corcoran, Effects of metallurgical variables on dealloying corrosion, in ASM
Handbook, Vol. 13A, Corrosion: Fundamentals, Testing, and Protection, ASM Interna-
tional, Materials Park, OH, 2003, pp. 287–293.
20. R. B. Abrams, Trans. Am. Chem. Soc. 42, 39 (1922).
21. H. W. Pickering, J. Electrochem. Soc. 115, 143 (1968).
22. H. W. Pickering and C. Wagner, J. Electrochem. Soc. 114, 698 (1967).
23. A. J. Forty and G. Rowlands, Philos. Mag. A 43, 171 (1981).
24. K. Sieradzki, N. Dimitrov, D. Movrin, C. McCall, N. Vasiljevic, and J. Erlebacher, J. Elec-
trochem. Soc. 149, B370 (2002).
25. K. Sieradzki, J. Electrochem. Soc. 140, 2868 (1993).
26. E. Polushkin and H. Shuldener, Min. Metall. Eng. 161, 214 (1945).
27. P. Elliott, Materials selection for corrosion control, in ASM Handbook, Vol. 13A, Cor-
rosion: Fundamentals, Testing, and Protection, ASM International, Materials Park, OH,
2003, pp. 917–918.
28. R. S. Lenox and P. A. Hough, ASHRAE J. November (1995).
29. D. R. McIntyre and C. P. Dillon, Guidelines for Preventing Stress Corrosion Cracking
in the Chemical Process Industries, Publication 15, Materials Technology Institute of
the Chemical Process Industries, 1985.
30. H. Uhlig and J. Sansone, Mater. Prot. 3, 21 (1964).
31. N. McKinney and H. Hermance, Stress Corrosion Testing, Special Technical Publication
No. 425, p. 274, American Society for Testing and Materials, Philadelphia, PA, 1967.
32. E. Mattsson, Electrochim. Acta 3, 279 (1960–1961).
33. H. Johnson and J. Leja, Corrosion 22, 178 (1966).
34. H. Uhlig, K. Gupta, and W. Liang, J. Electrochem. Soc. 122, 343 (1975).
35. A. Bailey, J. Inst. Metals 87, 380 (1959).
36. G. Edmunds in Symposium on Stress Corrosion Cracking of Metals, ASTM–AIME,
Philadelphia, 1945, p. 67.
37. R. Bakish and W. Robertson, J. Electrochem. Soc. 103, 320 (1956).
38. E. Pugh, J. H. Craig, and A. Sedriks, in Proceedings of Conference Fundamental Aspects
of Stress Corrosion Cracking, National Association of Corrosion Engineers, Houston,
TX, 1969, p. 118; see also S. Shimodaira and M. Takano, p. 202.
39. J. A. Beavers, in Stress-Corrosion Cracking, R. H. Jones, editor, ASM International,
PROBLEMS 381
40. F. A. Champion, Symposium on Internal Stresses in Metals and Alloys, Institute of

Metals, London, 1948, p. 468.
41. H. L. Logan, J. Res. Natl. Bur. Stand. 48(2), 99 (1952).
42. D. Thompson and A. Tracy, Min. Metall. Eng. 185, 100 (1949).
43. N. Magnani, Corrosion 36, 260 (1980).
44. R. H. Jones, Stress-corrosion cracking, in ASM Handbook, Vol. 13A, Corrosion: Fun-
p. 362.
45. R. C. Newman, T. Shahrabi, and K. Sieradzki, Scr. Metall. 23, 71 (1989).
46. U.S. Military Specification MIL-C-15726 E (Ships), August 20, 1965.
47. L. Eiselstein, B. Syrett, S. Wing, and R. Caligiuri, Corros. Sci. 23, 223 (1983).
48. W. Stewart and F. LaQue, Corrosion 8, 259 (1952).
GENERAL REFERENCES
J. A. Beavers, Stress-corrosion cracking of copper alloys, in Stress-Corrosion Cracking,

R. H. Jones, editor, ASM International, Materials Park, OH, 1992, pp. 211–231.
A. Cohen, Corrosion of copper and copper alloys, in ASM Handbook, Vol. 13B, Corrosion:
Materials, ASM International, Materials Park, OH, 2005, pp. 125–163.
C. A. C. Sequeira, Corrosion of copper and copper alloys, in Uhlig’s Corrosion Handbook,
PROBLEMS
1. Calculate the equilibrium constant at 25°C for the reaction Cu + Cu2+ → 2Cu+.
Since equilibrium tends to be maintained between ions and metal, which
valence ion predominates when Cu is dissolved anodically? (Data: Cu2+ + 2e−
→ Cu, φ° = 0.337 V; Cu+ + e− → Cu, φ° = 0.521 V.)
2. As in Problem 1, estimate, from the analogous equilibrium constant, which

valence ion predominates when Cr in the active state is dissolved anodically.
(Data: Cr2+ + 2e− → Cr, φ° = −0.91 V; Cr3+ + 3e− → Cr, φ° = −0.74 V.)
Answers to Problems
1. 6.1 × 10−7; Cu2+
2. Cr2+ predominates.
21
ALUMINUM AND
ALUMINUM ALLOYS
21.1 ALUMINUM
Al 3+ + 3e − → Al φ = −1.7 V
Aluminum is a lightweight metal (density = 2.71 g/cm3) having good corrosion

resistance to the atmosphere and to many aqueous media, combined with good
electrical and thermal conductivity. It is very active in the Emf Series (Section
3.8), but becomes passive on exposure to water. The theoretical potential–pH
domains for immunity, corrosion, and passivation can be seen from Fig. 4.3
(Section 4.4). Although oxygen dissolved in water improves the corrosion resis-
tance of aluminum, its presence is not necessary to achieve passivity, indicating
that the Flade potential (Section 6.2) of aluminum is active with respect to the
hydrogen electrode. It is usually assumed that the passive film is composed of
aluminum oxide, which, for air-exposed aluminum, is estimated at about 2–10 nm
(20–100 Å) in thickness. The observed corrosion behavior of aluminum is sensi-
tive to small amounts of impurities in the metal; all these impurities, with the
exception of magnesium, tend to be cathodic to aluminum. In general,
the high-purity metal is much more corrosion-resistant than commercially pure

383
384 ALUMINUM AND ALUMINUM ALLOYS
aluminum, which, in turn, is usually more resistant than aluminum alloys.* Some
of the aluminum alloys produced commercially in the United States are listed in
Table 21.1. For a complete list, the reference given in the table should be
consulted.
21.1.1 Clad Alloys

Pure aluminum is soft and weak; it is alloyed, therefore, largely to obtain increased
strength. In order to make use of the good corrosion resistance of pure aluminum,
a high-strength alloy may be sandwiched between pure aluminum or one of the
more corrosion-resistant alloys (e.g., 1% Mn–Al) active in the Galvanic Series
with respect to the inner alloy. This combination is called alclad or clad. The clad
structure, metallurgically bonded at the two interfaces, provides cathodic protec-
tion to the inner alloy by sacrificial action of the outer layers, similar to that
provided by a zinc coating on steel. In addition to cathodically protecting against
pitting corrosion, the less noble coatings also protect against intergranular cor-
rosion and stress-corrosion cracking, especially if the high-strength inner alloy
should become sensitized through fabrication procedures or by accidental expo-
sure to high temperatures.
21.1.2 Corrosion in Water and Steam

Aluminum tends to pit in waters containing Cl−, particularly at crevices or at
stagnant areas where passivity breaks down through the action of differential
aeration cells. The mechanism is analogous to that described for the stainless
steels (Section 19.2.4.1) including an observed critical potential below which
pitting corrosion does not initiate [3, 4]. Traces of Cu2+ (as little as 0.1 ppm) or of
Fe3+ in water react with aluminum, depositing metallic copper or iron at local
sites. The copper or iron, being efficient cathodes, shift the corrosion potential in
the noble direction to the critical potential, thereby both initiating pitting and,
by galvanic action, stimulating pit growth. For this reason, aluminum is not a
satisfactory material for piping to handle potable or industrial waters, which all
contain traces of heavy metal ions. On the other hand, for distilled water or for
a water from which heavy metal ions have been removed, aluminum is satisfac-
tory. Aluminum piping of high-purity metal or of type 1100 has been used satis-
factorily for distilled water lines over many years.
Extraneous anions in dilute chloride solutions act as pitting inhibitors by
shifting the critical pitting potential to more noble values [4]. The following ions
are effective in decreasing order: nitrate > chromate > acetate > benzoate >
sulfate.
*One exception is known with reference to intergranular disintegration of high-purity aluminum in

steam or pure water at temperatures above 125°C (260°F). The presence of iron as an impurity in
lower-grade metal avoids this type of attack or raises the temperature at which it occurs (>200°C for
type 1100) [1, 2].
ALUMINUM
TABLE 21.1. Composition Limits for Some Wrought Aluminum Alloysa

Alloy Maximum Amounts Specified (%)b
AA No.c UNS No. Si Fe Cu Mn Mg Cr Zn Ti
1100 A91100 0.95 (Si + Fe) 0.05–0.20 0.05 0.10

2017 A92017 0.2–0.8 0.7 3.5–4.5 0.40–1.0 0.40–0.8 0.10 0.25 0.15
2024 A92024 0.50 0.50 3.8–4.9 0.30–0.9 1.2–1.8 0.10 0.25 0.15
3003 A93003 0.6 0.7 0.05–0.2 1.0–1.5 0.10
3004 A93004 0.30 0.7 0.25 1.0–1.5 0.8–1.3 0.25
5050 A95050 0.40 0.7 0.20 0.10 1.1–1.8 0.10 0.25
5052 A95052 0.25 0.40 0.10 0.10 2.2–2.8 0.15–0.35 0.10
5056 A95056 0.30 0.40 0.10 0.05–0.20 4.5–5.6 0.05–0.20 0.10
d
6053 A96053 0.35 0.10 1.1–1.4 0.15–0.35 0.10
6061 A96061 0.40–0.8 0.7 0.15–0.40 0.15 0.8–1.2 0.04–0.35 0.25 0.15
6063 A96063 0.20–0.6 0.35 0.10 0.10 0.45–0.9 0.10 0.10 0.10
7072 A97072 0.7 (Si + Fe) 0.10 0.10 0.10 0.8–1.3
7075 A97075 0.40 0.50 1.2–2.0 0.30 2.1–2.9 0.18–0.28 5.1–6.1 0.20
a
Aluminum Standards and Data 2003, The Aluminum Association, Inc., Washington, D.C., March 2003, pp. 6-5–6-6.
b
Composition in percent by weight maximum except when composition ranges are given.
c
Code for major alloying element: 1XXX, >99.00% Al; 2XXX, Cu; 3XXX, Mn; 4XXX, Si; 5XXX, Mg; 6XXX, Si + Mg; 7XXX, Zn.
d
45–65% of the Mg content.
385
In uncontaminated seawater in the tropical environment of Panama, com-

mercially pure aluminum (1100) or 0.6% Si, 0.8% Mg, 0.2% Cu–Al alloy
(6061-T) corroded at decreasing rates with time. After 16 years of exposure,
the total weight losses were 67 and 63 g/m2, and the corresponding observed
deepest pits were 0.84 and 2.0 mm (0.033 and 0.079 in.), respectively, for small-
size test panels [5]. At the same location in fresh water, probably contami-
nated with heavy metals, the corresponding weight losses for 16 years were
higher—347 and 103 g/m2— and the deepest pits measured 2.8 mm (0.11 in.)
each.
Various commercial aluminum alloys immersed in seawater at Key West,
Florida, for 368 days pitted or not according to their corrosion potentials [6].
Alloys with corrosion potentials ranging from −0.4 to −0.6 V (S.H.E.) (most of
which contained some alloyed copper) showed a mean depth of pitting equal to
0.15–0.99 mm (0.006–0.039 in.), whereas those alloys of more active potential
(−0.7 to −1.0 V) were essentially not pitted. These potential ranges can be com-
pared with the critical pitting potential of pure aluminum measured in 3% NaCl,
equal to −0.45 V (see Section 6.6). Coupling of susceptible alloy panels to a
smaller-area panel of an active aluminum alloy (see Section 13.3.1), which polar-
ized the couple to approximately −0.85 V (S.H.E.), succeeded in largely prevent-
ing pitting over the same period of time. These field tests support the concept of
critical potentials below which, in the absence of crevices, neither aluminum nor
its alloys undergo pitting corrosion.
As the temperature increases, the corrosion rate of type 1100 in deaerated
distilled water increases, but the value at 70°C is still very low, being about
0.007 gmd [1]. This rate is reduced to 0.004 gmd in the presence of 10−3N H2O2
and still lower by 2 ppm K2Cr2O7. At 150°C the rate in distilled water is about
0.04 gmd, and at 200°C it is 0.25 gmd, with the attack in all these instances being
uniform and without marked pitting. At higher temperatures (e.g., 275°C), but
usually only after several days of exposure, the rate becomes more rapid by a
factor of 10–20 times, and corrosion proceeds mostly along grain boundaries,
causing rapid failure. At 315°C, complete disintegration to Al2O3 may occur
within a few hours. It is important to note that this catastrophic corrosion does
not occur at the cited high temperatures if the aluminum is coupled to a sufficient
area of stainless steel or of zirconium, both of which are cathodic to aluminum.
The same beneficial effect is obtained by small alloying additions of nickel and
iron. For example, the corrosion rate at 350°C for type 1100 aluminum alloyed
with 1% Ni is about 1.8 gmd [1].
The beneficial effect of cathodic areas can be explained [7] as one of anodic
passivation or anodic protection of aluminum in the same manner as alloying
additions or coupling of platinum or palladium to stainless steels or to titanium
passivate these metals in acids (Section 6.4).
At 500–540°C, the oxidation rate of pure aluminum in steam is appreciably
lower than at 300–450°C [8], presumably because a more protective oxide film
forms within the higher temperature range.
ALUMINUM 387
21.1.3 Effect of pH
Aluminum corrodes more rapidly both in acids and in alkalies compared to dis-
tilled water, with the rates in acids depending on the nature of the anion. Figure
21.1 provides data at 70–95°C [1], showing that the minimum rate, when using
sulfuric acid for adjustment of pH in the acid region, occurs between pH 4.5 and
7. At room temperature, the minimum rate occurs in the pH range approximating
4–8.5. Corrosion rates of aluminum in the alkaline region greatly increase with
pH, unlike iron and steel, which remain corrosion-resistant. The reason for this
difference is that Al3+ is readily complexed by OH−, forming AlO−2 in accord
with
Figure 21.1. Effect of pH on corrosion of commercially pure aluminum (1100), aerated solu-
tions; pH, measured at room temperature, was adjusted with H2SO4 or NaOH. Most solutions
contained 1–10 × 10−5 N H2O2, 68 ppm CaSO4, 30 ppm MgSO4, 1–2 ppm NaCl (J. Draley and
W. Ruther).
3
Al + NaOH + H 2O → NaAlO2 + H 2 (21.1)
2
This reaction proceeds rapidly at room temperature, whereas for iron a similar
reaction forming NaFeO2 and Na2FeO2 requires concentrated alkali and high
temperatures.
21.1.4 Corrosion Characteristics

Aluminum is characterized by (1) sensitivity to corrosion by alkalies and (2)
pronounced attack by traces of copper ions in aqueous media. In addition, alu-
minum is subject to rapid attack by (3) mercury metal and mercury ions and (4)
anhydrous chlorinated solvents (e.g., CCl4, ethylene dichloride, and propylene
dichloride) [9, 10].
The rate of attack can be appreciable in either dilute or concentrated alkalies.
For this reason, when aluminum is cathodically protected, overprotection must be
avoided in order to ensure against damage to the metal by accumulation of alkalies
at the cathode surface. Lime, Ca(OH)2, and some of the strongly alkaline organic
amines (but not NH4OH) are corrosive. Fresh Portland cement contains lime and
is also corrosive; hence, aluminum surfaces in contact with wet concrete may
evolve hydrogen visibly. The corrosion rate is reduced when the cement sets, but
continues if the concrete is kept moist or contains deliquescent salts (e.g., CaCl2).
A drop of mercury in contact with an aluminum surface rapidly breaks
down passivity accompanied by amalgamation (i.e., formation of an aluminum
amalgam). In the presence of moisture, the amalgamated metal quickly converts
to aluminum oxide, causing perforation of piping or sheet. Mercury ions present
in solution in only trace amounts similarly accelerate corrosion, producing intol-
erably high rates of attack.
Aluminum tanks in aircraft fuel systems are subject to corrosion resulting
from the growth of microbiological constituents in kerosene fuel [11–16]. Until
recently, the most important of these constituents was the fungus Cladosporium
resinae [11]. Fungi produce highly corrosive organic acids that corrode aluminum
fuel tanks. Temperature and the availability of water are reported to be the prin-
cipal factors determining whether and where microbial growth occurs. Growth
initiates in water deposits at the interface with the fuel, with the resulting fungus
adhering to the tank lining. The growth rate is controlled by temperature and is
greatest at about 30–35°C. Subsequent corrosion has been explained on the basis
of water-soluble organic acids produced by the metabolism of various microor-
ganisms and also on the basis of oxygen depletion beneath the growing microbial
layer (differential aeration cell).
The changes in jet fuel and jet fuel additives that have taken place in recent
years have also brought about a shift in the microbial community in aircraft fuel.
The bacteria isolated from aircraft jet fuel tanks have been found to be closely
related to Bacillus, and they do have the potential to cause microbiologically
influenced corrosion (MIC) [11, 17, 18].
ALUMINUM 389
Although MIC may be controlled by adding a biocide to the fuel, this solu-
tion may create new problems; for example, biocides may selectively enrich a
population of bacteria capable of biocide resistance [12].
21.1.4.1 Reaction with Carbon Tetrachloride. Severe accidents have

been caused by the rapid reaction of aluminum with anhydrous chlorinated sol-
vents, such as in the degreasing of castings, in ball milling of aluminum flake with
carbon tetrachloride (CCl4), or even in the case of aluminum used as a container
at room temperature for mixed chlorinated solvents. The reaction with CCl4, for
example, has been shown to be
2 Al + 6CCl 4 → 3C 2Cl 6 + 2 AlCl 3 (21.2)
forming hexachloroethane, C2Cl6, with evolution of heat. The corrosion rate for
99.99% Al in boiling anhydrous CCl4 is very high—for example, 3750 gmd (20 ipy)
[19]. Should the temperature reach the melting point of aluminum, the reaction
may proceed explosively. An induction time of about 55 min, during which cor-
rosion is negligible, precedes the rapid rate (Fig. 21.2). This induction time is
lengthened either by the presence of water in the CCl4 (480 min) or by some
alloying additions—for example, Mn or Mg (30 h for type 5052). On the other
hand, addition of AlCl3 or FeCl3 to CCl4 decreases the induction time to zero
without an appreciable effect on the corrosion rate. The corrosion rate of alumi-
num in water-saturated CCl4, following a prolonged induction time, is about twice
that in the anhydrous solvent (Fig. 21.3).
Figure 21.2. Weight loss as a function of time for 99.99% Al in boiling, distilled CCl4 contain-
ing 0.0011% H2O [19]. (Reproduced with permission. Copyright 1952, The Electrochemical
Society.)
Figure 21.3. Effect of water on corrosion rate of 99.99% Al in boiling CCl4 [19]. (Reproduced
with permission. Copyright 1952, The Electrochemical Society.)
In practice, volatile inhibitors are often added to chlorinated solvents in

order to suppress the fast reaction. Examples include various ketones, quinones,
and amines, which presumably react preferentially with and destroy free radicals
(e.g., ·CCl3 and ·Cl). The latter are considered to play an important part in the
reaction mechanism [20]. A proposed sequence of intermediate reactions, for
example, is the following:
CCl 4 →iCCl 3 + iCl

Initiation
Al + iCl → AlCl
AlCl + CCl 4 → AlCl 2 + iCCl 3

AlCl 2 + CCl 4 → AlCl 3 + iCCl 3
Propagation
AlCl 3 + CCl 4 → CCl +3[AlCl 4]−
CCl +3[AlCl 4]− → AlCl 3 + iCCl 3 + iCl
2iCCl 3 → C 2Cl 6
Termination
i
Cl + iCCl 3 → CCl 4
Subsequent investigations by others have confirmed the presence of ·CCl3 and

various of the proposed intermediate reacting species [21,22].
Water itself may react with and destroy initiating species until the water is
consumed by chemical reaction or until sufficient AlCl3 forms. Hence, the induc-
ALUMINUM 391
tion time is extended when water is present in the solvent. By the same token,
in anhydrous CCl4, vacuum treatment of aluminum specimens results in a shorter
induction time of 5 min compared to 55 min not treated, probably by reducing
the H2O content of the oxide film. Substances like AlCl3 decrease the induction
time by forming a complex with CCl4 that later dissociates into free radicals
taking part in the chain reaction. Similarly, alloying elements like magnesium are
considered to react preferentially with free radicals, accounting for the observed
improved corrosion resistance of magnesium–aluminum alloys to CCl4 compared
to pure aluminum. The behavior of alloying constituents in general (often oppo-
site to their effect in aqueous environments), the observed lack of effect of gal-
vanic coupling or of an impressed nominal voltage on the rate, along with the
same observed corrosion rate in the vapor phase as in the boiling liquid are a
strong arguments that the reaction does not follow an electrochemical mecha-
nism. In addition to analytical evidence for ·CCl3, (the species that probably
accounts for the red color of CCl4 reacting with Al), the ease with which many
added organic substances suppress the fast reaction (free radicals are very reac-
tive) also supports the free-radical mechanism.
In summary, aluminum (type 1100) is resistant to the following:
1. Hot or cold NH4OH.

2. Hot or cold acetic acid. Highest rates of attack are for the boiling 1–2%
acid. Ninety-nine percent acetic acid is not appreciably corrosive, but
removal of the last 0.5% H2O increases attack over a hundredfold. Formic
acid and Cl− contamination also increase attack. Aluminum is resistant to
citric, tartaric, and malic acids.
3. Fatty acids. Aluminum equipment is used for distillation of fatty acids.
4. Nitric acid, >80% up to about 50°C (120°F) [23] (see Fig. 21.4).
5. Distilled water.
6. Atmospheric exposure. Excellent resistance to rural, urban, and industrial
atmospheres; lesser resistance to marine atmospheres.
7. Sulfur, sulfur atmospheres, and H2S. Aluminum is used for mining of
sulfur.
8. Fluorinated refrigerant gases, such as Freon, but not to methyl chloride or
bromide.
Aluminum is not resistant to the following:
1. Strong acids, such as HCl and HBr (dilute or concentrated), H2SO4 (sat-
isfactory for special applications at room temperature below 10%), HF,
HClO4, H3PO4, and formic, oxalic, and trichloroacetic acids.
2. Alkalies. Lime and fresh concrete are corrosive, as well as strong alkalies;
for example, NaOH and the very alkaline organic amines. Corrosion by
soap solutions can be inhibited by adding a few tenths percent of sodium
silicate (not effective for strong alkalies).
Figure 21.4. Corrosion rates of commercially pure aluminum (1100) in nitric acid, room
temperature [23]. (Copyright NACE International 1961.)
3. Mercury and mercury salts.

4. Seawater. Pitting occurs at crevices and surface deposits, especially when
trace amounts of heavy metal ions are present.
5. Waters containing heavy metal ions (e.g., mine waters or waters previously
passing through copper, brass, or ferrous piping).
6. Chlorinated solvents.
7. Anhydrous ethyl, propyl, or butyl alcohols at elevated temperatures. A
trace of water acts as an inhibitor [23].
8. Contact with wet woods, in particular beech wood [24]. Any wood impreg-
nated with copper preservatives is especially damaging.
(For behavior in soils, see Section 10.3.)
21.1.5 Galvanic Coupling

Although cadmium has the nearest potential to that of aluminum in many envi-
ronments, and cadmium-plated steel screws, bolts, trim, and so on, can be used in
ALUMINUM ALLOYS 393
direct contact with aluminum, nevertheless, cadmium is now recognized as a

biocumulative poison with toxic effects similar to those of mercury and lead;
cadmium plating is forbidden on most or all parts in many countries [25]. Tin
coatings are reported to be satisfactory. Zinc is somewhat further removed in
potential, but it is also usually satisfactory. Zinc is anodic to, and, hence, cathodi-
cally protects, aluminum against initiation of pitting in neutral or slightly acidic
media (see Section 13.7.1). In alkalies, however, the polarity reverses, and zinc
accelerates the corrosion of aluminum. Magnesium is anodic to aluminum, but
the potential difference and the resultant current flow when the metals are
coupled (e.g., in seawater) is so high that aluminum may be overprotected cath-
odically with resultant damage to aluminum. Aluminum is damaged in this respect
to a lesser extent when alloyed with magnesium. High-purity aluminum, it is
reported, can be coupled to magnesium without damage to either metal [26],
because galvanic currents are reduced in the absence of iron, copper, and nickel
impurities, which act as efficient cathodes.
It is imperative that aluminum never be coupled to copper or copper alloys,
because of the resulting damage to aluminum. In this connection, it is also impor-
tant to avoid contact of aluminum with rain water that has washed over copper
flashing or gutters because of the damage caused by small amounts of Cu2+ dis-
solved in such water.
In rural areas, coupling of steel to aluminum is usually satisfactory, but in
seacoast areas attack of aluminum is accelerated. In fresh waters, aluminum may
be anodic or cathodic to steel, depending on small composition differences of the
water.
21.2 ALUMINUM ALLOYS
The usual alloying additions to aluminum in order to improve physical properties

include Cu, Si, Mg, Zn, and Mn. Of these, manganese may actually improve the
corrosion resistance of wrought and cast alloys. One reason is that the compound
MnAl6 forms and takes iron into solid solution. The compound (MnFe)Al6 settles
to the bottom of the melt, in this way reducing the harmful influence on corrosion
of small quantities of alloyed iron present as an impurity [27]. No such incorpora-
tion occurs in the case of cobalt, copper, and nickel, so that manganese additions
would not be expected to counteract the harmful effects of these elements on
corrosion behavior.
The Duralumin alloys (e.g., types 2017 and 2024) contain several percent
copper, deriving their improved strength from the precipitation of CuAl2 along
slip planes and grain boundaries. Copper is in solid solution above the homoge-
nizing temperature of about 480°C (900°F) and, on quenching, remains in solu-
tion. Precipitation takes place slowly at room temperature with progressive
strengthening of the alloy. Should the alloy be quenched from solid–solution
temperatures into boiling water, or, after quenching should it be heated (artifi-
cially aged) above 120°C (250°F), the compound CuAl2 forms preferentially
along the grain boundaries. This results in a depletion of copper in the alloy
adjacent to the intermetallic compound, accounting for grain boundaries anodic
to the grains, and a marked susceptibility to intergranular corrosion. Prolonged
heating (overaging) restores uniform composition alloy at grains and grain inter-
faces, thereby eliminating susceptibility to this type of corrosion, but at some
sacrifice of physical properties. In practice, the alloy is quenched from about
490°C (920°F), followed by room-temperature aging.
Exfoliation is a related type of anodic path corrosion in which attack of rolled
or extruded aluminum alloy results in surface blisters followed by separation of
elongated slivers or laminae of metal. It occurs in various types of aluminum
alloys in addition to the copper-bearing series. Proper heat treatment may allevi-
ate such attack.
Exfoliation is commonly experienced on exposure of susceptible aluminum
alloys to marine atmospheres. Simulation in the laboratory is accomplished by
controlled intermittent spray with 5% NaCl containing added acetic acid to pH
3 at 35–50°C (95–120°F) [28]. In practice, severe exfoliation corrosion has been
experienced in water irrigation piping constructed of type 6061 alloy [29]. The
cause in this instance was ascribed to pipe fabrication methods and presence of
excess amounts of impurity elements (e.g., Fe, Cu, and Mn).
21.2.1 Stress-Corrosion Cracking

Pure aluminum is immune to stress-corrosion cracking (S.C.C.). Should a Duralu-
min alloy, on the other hand, be stressed in tension in the presence of moisture,
it may crack along the grain boundaries. Sensitizing the alloy by heat treatment,
as described previously, makes it more susceptible to this type of failure. In aging
tests at 160–205°C (320–400°F), maximum susceptibility was observed at times
somewhat short of maximum tensile strength [30]. Hence, in heat-treatment
procedures, it is better practice to aim at a slightly overaged rather than an
underaged alloy.
Magnesium alloyed with aluminum increases susceptibility to S.C.C., espe-
cially when magnesium is added in amounts >4.5%. To avoid such failures, slow
cooling (50°C/h) from the homogenizing temperature is necessary supposedly in
order to coagulate the β phase (Al3Mg2), a process that is promoted by addition
of 0.2% Cr to the alloy [31]. Microstructures that are resistant to S.C.C. are those
either with no precipitate along grain boundaries or with precipitate distributed
as uniformly as possible within grains [32].
For structural components in automotive applications, the Aluminum Asso-
ciation guidelines [33, 34] recommend alloys with a maximum of 3% Mg where
there is exposure for long periods to temperatures greater than about 75°C
(167°F). If an alloy of higher Mg content is being considered, the thermal expo-
sure of the part during its lifetime should be established, and realistic, full-
component testing should be carried out as part of a detailed materials assessment
to evaluate and qualify the specific alloy under consideration. Following these
guidelines has led to successful use of, for example, alloy 5182, a 4.5% Mg alloy,
ALUMINUM ALLOYS 395
in structural components of the Honda NSX with no known record of field fail-
ures caused by SCC [35, 36].
Edeleanu [37] showed that cathodic protection stopped the growth of cracks
that had already progressed into the alloy immersed in 3% NaCl solution. On
aging the alloy at low temperatures, maximum susceptibility to S.C.C. occurred
before maximum hardness values were reached. This behavior paralleled that of
a Duralumin alloy cited previously. Accordingly, Edeleanu proposed that the
susceptible material along the grain boundary which caused cracking was not the
equilibrium β phase responsible for hardness, but instead was made up of mag-
nesium atoms segregating at the grain boundary before the intermetallic com-
pound formed. On this basis, susceptibility to S.C.C. decreased on continued aging
of the alloy because the separated β phase consumed the original segregated
grain-boundary material responsible for susceptibility. A similar mechanism
probably applies to the copper–aluminum alloy series.
High concentrations of zinc in aluminum (4–20%) also induce susceptibility
to cracking of the stressed alloys in the presence of moisture. Traces of H2O, for
example, contained in the surface oxide film are sufficient to cause cracking;
carefully baked-out specimens in dry air do not fail [38]. Oxygen is not necessary,
nor is a liquid aqueous phase required. These conditions, plus the susceptibility
of a high-strength aluminum alloy (7075) to failure in organic solvents [39],
suggest that a possible mechanism of failure may be one of stress-sorption crack-
ing caused by adsorbed water or organic molecules on appropriate defect sites
of the strained alloy. Nevertheless, the mechanism of S.C.C. of aluminum alloys
is complex, involving several time-dependent interactions that are difficult to
evaluate independently, such as the roles of anodic dissolution, hydrogen embrit-
tlement, and grain boundary precipitates in the initiation and propagation of
cracks [40–42]. Understanding has been sufficient, however, to permit new alu-
minum alloys to be developed with high strength combined with improved resis-
tance to corrosion, including S.C.C., and such alloys are now used, for example,
on Boeing 777 aircraft [41].
Many high-strength aluminum alloys are available (some are listed in Table
21.1); specific composition ranges and heat treatments for these alloys are usually
chosen with the intent of minimizing susceptibility to S.C.C. Solution heat-
treatment temperature affects stress-corrosion susceptibility by altering the
grain-boundary composition as well as the alloy metallurgical microstructure [42,
43]. Service temperatures—especially those above room temperature—that can
cause artificial aging sometimes induce susceptibility followed by premature
failure in the presence of moisture or sodium chloride solutions. Susceptibility of
any of the wrought alloys is greatest when stressed at right angles to the rolling
direction (in the short transverse direction), probably because more grain-bound-
ary area of elongated grains along which cracks propagate comes into play.
As mentioned earlier, cladding of alloys can serve to cathodically protect
them from either intergranular corrosion or S.C.C. Compressive surface stresses
are effective for avoiding S.C.C.; hence, practical structures are sometimes shot
peened.
REFERENCES
1. J. Draley and W. Ruther, Corrosion 12, 441t, 480t (1956).

2. T. Pearson and H. Phillips, Corrosion of pure aluminum, Met. Rev. (London) 2, 305,
(1957).
3. H. Kaesche, Z. Phys. Chem. N.F. 34, 87, (1962).
4. H. Böhni and H. Uhlig, J. Electrochem. Soc. 116, 906, (1969).
5. C. Southwell, A. Alexander, and C. Hummer, Jr., Mater. Prot. 4, 30, (1965).
6. R. Groover, T. Lennox, Jr., and M. Peterson, Mater. Prot. 8, 25, (1969).
7. D. MacLennan, A. Macmillan, and J. Greenblatt, The corrosion of aluminum and alumi-
num alloys in high temperature water, in Proceedings of the First International Con-
gress on Metallic Corrosion, Butterworths, London, 1961, p. 429.
8. R. Hart and J. Maurice, Corrosion 21, 222, (1965).
9. A. Hamstead, G. Elder, and J. Canterbury, Corrosion 14, 189t (1958).
10. E. Ghali, Aluminum and aluminum alloys, in Uhlig’s Corrosion Handbook, 2nd edition,
11. B. J. Little and J. S. Lee, Microbiologically Influenced Corrosion, Wiley, New York, 2007,
pp. 195–201.
12. J.-D. Gu, T. E. Ford, and R. Mitchell, Microbiological corrosion of metals, in Uhlig’s
923–924.
13. J. Elphick, in Microbial Aspects of Metallurgy, J. D. A. Miller, editor, American Elsevier,
New York, 1970, pp. 157–172.
14. H. Hedrick, Materials Prot. 9(1), 27 (1970).
15. P. B. Park, in Microbial Aspects of the Deterioration of Materials, edited by R. Gilbert
and D. Lovelock, Academic Press, London, 1975, pp. 105–126.
16. R. Salvarezza, M. de Mele, and H. Videla, Corrosion 39, 26, (1983).
17. C. J. McNamara, T. D. Perry, N. Wolf, R. Mitchell, R. Leard, and J. Dante, Corrosion of
aluminum alloy 2024 by jet fuel degrading microorganisms, CORROSION/2003,
Paper No. 03568, NACE International, Houston, TX, 2003.
18. C. J. McNamara, T. D. Perry IV, R. Leard, K. Bearce, J. Dante, and R. Mitchell, Biofouling
221(5/6), 257 (2005).
19. M. Stern and H. Uhlig, J. Electrochem. Soc. 99, 381, 389, (1952).
20. M. Stern and H. Uhlig, J. Electrochem. Soc. 100, 543, (1953).
21. W. Archer and M. Harter, Corrosion 34, 159, (1978).
22. R. Ellialtioglu, H. White, L. Godwin, and T. Wolfram, J. Chem. Phys. 72(10), 5291
(1980).
23. E. Cook, R. Horst, and W. Binger, Corrosion 17, 25t (1961).
24. R. Farmer, Metallurgia 68, 161, (1963).
25. T. Mooney, Electroplated coatings, in ASM Handbook, Vol. 13A, Corrosion: Funda-
p. 778.
26. M. Bothwell, J. Electrochem. Soc. 106, 1014, (1959).
27. M. Whitaker, Metal Ind. 80, 1, (1952).
28. B. Lifka and D. Sprowls, Corrosion 22, 7, (1966).

29. J. Zahavi and Y. Yahalom, J. Electrochem. Soc. 129, 1181, (1982).
30. W. Robertson, Trans. Am. Inst. Min. Metall. Eng. 166, 216 (1946); see also U. Evans, The
Corrosion and Oxidation of Metals, Arnold, London, 1960, p. 674.
31. P. Brenner, Metal Progr. 65, 112, (1954).
32. J. G. Kaufman, Corrosion of aluminum and aluminum alloys, in ASM Handbook, Vol.
13B, Corrosion: Materials, ASM International, Materials Park, OH, 2003, pp.
105–106.
33. Aluminum: The Corrosion Resistant Automotive Material, Publication AT7, Aluminum
Association, 2001.
34. Aluminum for Automotive Body Sheet Panels, Publication AT3, Aluminum Associa-
tion, 1998.
35. G. Courval, Corrosion of aluminum components in the automotive industry, in ASM
36. Y. Komatsu et al., Application of all aluminum automotive body for Honda NSX,
Technical Paper 910548, Society of Automotive Engineers, 1991.
37. C. Edeleanu, J. Inst. Metals 80, 187, (1951).
38. G. Wasserman, Z. Metall. 34, 297, (1942).
39. H. Paxton and R. Procter, in Fundamental Aspects of Stress Corrosion Cracking, R.
Staehle et al., editor, National Association of Corrosion Engineers, Houston, TX, 1969,
p. 509.
40. N. J. H. Holroyd, Environment-induced cracking of high-strength aluminum alloys, in
Proceedings of the First International Conference on Environment-Induced Cracking
of Metals, 1988, NACE-10, R. P. Gangloff and M. B. Ives, editors, National Association
of Corrosion Engineers, Houston, TX, 1990, pp. 311–345.
41. V. S. Agarwala, Corrosion in the military, in ASM Handbook, Vol. 13C, Corrosion:
Environments and Industries, ASM International, Materials Park, OH, 2006, pp.
132–133.
42. J. G. Kaufman, Corrosion of aluminum and aluminum alloys, in ASM Handbook, Vol.
13B, Corrosion: Materials, ASM International, Materials Park, OH, 2005, pp.
105–106.
43. C. Shastry, M. Levy, and A. Joshi, Corros. Sci. 21, 673, (1981).
GENERAL REFERENCES
V. S. Agarwala and G. M. Ugiansky, editors, New Methods for Corrosion Testing of Alumi-
num Alloys, STP 1134, ASTM, Philadelphia, 1992.
E. Ghali, Aluminum and aluminum alloys, in Uhlig’s Corrosion Handbook, 2nd edition,
N. J. H. Holroyd, Environment-induced cracking of high-strength aluminum alloys, in Pro-
ceedings of the First International Conference on Environment-Induced Cracking of
Metals, 1988, NACE-10, R. P. Gangloff and M. B. Ives, editors, National Association of
Corrosion Engineers, Houston, TX, 1990, pp. 311–345.
J. G. Kaufman, Corrosion of aluminum and aluminum alloys, in ASM Handbook, Vol. 13B,
Corrosion: Materials, ASM International, Materials Park, OH, 2003, pp. 95–124.
J. Snodgrass and J. Moran, Corrosion resistance of aluminum alloys, in ASM Handbook,
als Park, OH, 2003, pp. 689–691.
Stress-corrosion cracking of aluminum alloys, in Stress-Corrosion Cracking, R. H. Jones,
editor, ASM International, Materials Park, OH, 1992, pp. 233–249.
22
MAGNESIUM AND
MAGNESIUM ALLOYS
22.1 INTRODUCTION
Although magnesium and its alloys have long been perceived as rapidly corrod-
ing, it is possible, by appropriate alloy selection combined with good engineering
design and correctly applied surface treatment and protection schemes, to use
these materials successfully and obtain numerous benefits, including light weight,
high strength/weight ratio, high stiffness/weight ratio, and ease of machinability
[1]. In the original Volkswagen Beetle, magnesium alloys were successfully used
for the engine and for the transmission casings. Today, magnesium alloys are used
in consumer applications (e.g., cases for laptop computers and cameras), in the
automotive industry (transmission casings, engine blocks), and in the aerospace
industry (helicopter transmission and rotor housings). The corrosion behavior of
magnesium and its alloys and the principles behind successful use of these materi-
als are discussed in this chapter.
22.2 MAGNESIUM
Mg 2+ + 2e − → Mg φ = −2.34 V

399
400 MAGNESIUM AND MAGNESIUM ALLOYS
Several investigators have obtained evidence that magnesium dissolves

anodically to a large extent as Mg+ and that this ion in solution reduces water to
form Mg2+ plus H2 (see Section 13.6).
Magnesium has the lowest density (1.7 g/cm3) of all structural metals, having
about one-fourth the density of iron and one-third that of aluminum. This very
low density makes magnesium and magnesium alloys useful wherever low weight
is important, if not required.
Magnesium is also the most active metal in the Emf Series that is used for
structural purposes. The potential–pH diagram for magnesium and water (Fig.
4.4, Section 4.5) indicates the theoretical domains of corrosion, passivity, and
immunity. Magnesium corrodes over a wide range of potential and pH. At high
pH, in the region identified as passive, the magnesium hydroxide corrosion
product film is only partially protective. This low-density film allows electrolyte
to contact the underlying metal. In addition, the film ruptures because of the
higher molar volume of magnesium hydroxide compared to metallic magnesium,
resulting in the constant exposure of fresh metal [2].
Corrosion resistance of magnesium depends on purity of the metal even
more than the corrosion resistance of aluminum depends on its purity. Distilled
magnesium corrodes in seawater, for example, at the rate of 0.25 mm/y (0.01 ipy),
which is about twice the rate for iron, but commercial magnesium corrodes at
a rate 100–500 times higher, with visible hydrogen evolution. The impurities in
commercial magnesium largely responsible for the higher rate are iron and, to a
lesser extent, nickel and copper. Their effect becomes marked above a critical
concentration called the tolerance limit [3]. For iron, the tolerance limit is 0.017%;
similarly, for nickel and copper, it is 0.0005% and 0.1%, respectively (Fig. 22.1).
Additions of manganese or zinc to the metal raise these limits to higher values.
Manganese has been reported to surround iron particles and to render them
inactive as local cathodes [4]. An additional mechanism may involve formation
of an insoluble intermetallic compound that includes iron in its structure. This is
heavier than magnesium; hence, similar to the situation for aluminum (Section
21.2), it settles to the bottom of the melt, in this way reducing the Fe content of
the cast metal.
22.3 MAGNESIUM ALLOYS
Because unalloyed magnesium is not used extensively for structural applications,

it is the corrosion resistance of magnesium alloys that is of primary interest. To
enhance strength and resistance to corrosion, magnesium is alloyed with alumi-
num, lithium, zinc, rhenium, thorium, and silver, with minor additions of cerium,
manganese, and zirconium sometimes being used as well.
There are two major alloying systems:
1. Alloys containing 2–10% aluminum with minor additions of zinc and

manganese; these alloys are used up to 95–120°C (200–250°F), above
MAGNESIUM ALLOYS 401
Figure 22.1. Corrosion of magnesium in 3% NaCl, alternate immersion, 16 weeks, showing

tolerance limit for iron and beneficial effect of alloyed zinc and manganese [Figure 4 from J.
Hanawalt, C. Nelson, and J. Peloubet, Corrosion studies of magnesium and its alloys, Trans.
AIME, Inst. Metals Div. 147, 281 (1942)].
which temperature range both corrosion resistance and strength

deteriorate.
2. Alloys containing various elements (rare earths, zinc, thorium, and silver),
but not aluminum, and containing zirconium, which provides grain refine-
ment and improved mechanical properties; these alloys provide improved
elevated temperature properties compared to those in the first group.
Some alloys in both systems that are commonly available are listed in Table 22.1.
In the ASTM system for designating magnesium alloys, the first two letters indi-
cate the principal alloying elements: A, aluminum; E, rare earths; H, thorium; K,
zirconium; M, manganese; Q, silver; Z, zinc. The letter corresponding to the
element present in greater concentration is listed first; if the elements are in equal
concentration, they are listed alphabetically. The letters are followed by numbers
that indicate the nominal compositions of these alloying elements, rounded off
to the nearest whole number; for example, AZ91 indicates the alloy Mg–9Al–
1Zn. In addition, letters that are sometimes appended to the alloy designation
are assigned chronologically and usually indicate alloy improvements in purity
[5].
In saline solutions, the corrosion rate is controlled by the concentration and
distribution of the critical elements, iron, nickel, and copper, which create cathodic
sites of low hydrogen overpotential. For this reason, these elements are usually
controlled at low impurity levels.
Alloy purity, however, does not prevent galvanic corrosion that occurs if the
magnesium alloy is coupled, for example, to a steel bolt. Design to prevent gal-
vanic corrosion is, therefore, essential. In addition to the anode/cathode area
ratio, the conductivity and composition of the medium in which a couple is
immersed are controlling factors in the rate of galvanic corrosion. All commonly
used metals cause galvanic corrosion of magnesium in saline solutions, but zinc
plating the cathode (e.g., iron or steel) has been found to reduce the galvanic
corrosion of the magnesium to one-tenth the rate. In addition, a reduction in the
conductivity (e.g., changing from 3% NaCl to tap water), results in an even
greater reduction in the galvanic corrosion rate.
22.3.1 Stress-Corrosion Cracking

The magnesium alloys with greatest susceptibility to stress-corrosion cracking
(S.C.C.) are the Mg–Al alloys, and susceptibility increases with Al concentration.
Magnesium–zinc alloys have intermediate susceptibility, and alloys that contain
neither aluminum nor zinc are the most resistant [7].
Stress-corrosion cracking of magnesium alloys occurs in many environments,
including distilled water, seawater, and atmospheric environments in rural, urban,
industrial, and coastal areas. In water, dissolved oxygen accelerates S.C.C. and
deaeration retards it. S.C.C. in magnesium alloys is usually transgranular with
secondary cracks, or branching, and initiation usually occurs at pits. Although
several mechanisms for S.C.C. of magnesium alloys have been proposed, hydro-
gen embrittlement is most likely a factor [8].
Intergranular S.C.C. of magnesium alloys has also been reported, attributed
to a grain-boundary phase of Mg17Al12 that causes galvanic attack of the adjacent
matrix [8].
As in most systems in which S.C.C. occurs, both applied and residual stresses
are important. Welded components of magnesium alloys are normally stress-
relieved after welding to reduce the residual stresses that develop during welding.
MAGNESIUM ALLOYS 403
TABLE 22.1. Nominal Compositions of Some Magnesium Alloysa

Alloy Number Element (%) Product
Formb
ASTM UNS Al Zn Mn Ag Zr Th Re
M1 M15100 — — 1.5 — — — — W
AM50 M10500 5 — 0.3 — — — — C
AM60 M10600 6 — 0.2 — — — — C
AZ31 M11310 3 1 0.2 — — — — W
AZ61 M11610 6 1 0.2 — — — — W
AZ63 M11630 6 3 0.2 — — — — C
AZ80 M11800 8 0.5 0.2 — — — — C, W
AZ91 M11910 9 1 0.2 — — — — C
EZ33 M12331 — 2.5 — — 0.5 — 2.5 C
ZM21 — — 2 1 — — — — W
HK31 M13310 — 0.1 — — 0.5 3 — C, W
HZ32 M13320 — 2 — — 0.5 3 — C
QE22 M18220 — — — 2.5 0.5 — 2 C
QH21 M18210 — — — 2.5 0.5 1 1 C
ZE41 M16410 — 4.5 — — 0.5 — 1.5 C
ZE63 M16630 — 5.5 — — 0.5 — 2.5 C
ZK40 M16400 — 4.0 — — 0.5 — — C, W
ZK60 M16600 — 6.0 — — 0.5 — — C, W
a
Adapted from Ref. 6.
b
C, cast alloy; W, wrought alloy.
Resistance to S.C.C. may also be increased by using shot peening and other pro-
cesses that produce compressive residual stresses at the surface [8].
22.3.2 Coatings
Coatings provide an important strategy for protecting magnesium alloys from
corrosion. In light-truck applications, heads of bolts made from AZ91D were
protected from galvanic corrosion by using a nylon coating that was electrostati-
cally applied. Molded plastic caps were also found to be effective. Zinc alloy
coatings (e.g., 80Sn–20Zn) electroplated on magnesium and given a chromate
treatment were found to decrease the corrosion rate of magnesium by more than
90% in salt spray testing [9, 10].
Various protective anodized coatings are available as produced in electro-
lytes composed mainly of fluorides, phosphates, or chromates [11]. Anodizing
treatments result in porous coatings that provide excellent bases for subsequent
painting. Anodized magnesium castings are used successfully, for example, in
helicopter drive system components. In general, in aerospace applications where
extended component life and low maintenance costs are required, all surfaces of
magnesium alloys exposed to corrosive environments must be coated.
Driven by the need to reduce both gasoline consumption and greenhouse

gas production, the automotive industry is reducing vehicle weight to the extent
possible, and one approach being used is increasing the magnesium content of
automobiles. Large heavy automobile parts are particularly attractive candidates
for replacement by magnesium. The extent of corrosion protection required
depends on the severity of the environment; for example, for underbody and
wheel applications, comprehensive protection schemes are essential, including
protection against galvanic corrosion. Underbody wax-type coatings may provide
additional protection. One of the more recent developments in the automotive
industry is the application of Alloy AM50 for the front-end support assembly for
light-duty Ford trucks [12]. Magnesium alloys are also being used for air cleaner
covers, engine compartment grills, retractable headlight assemblies, clutch and
brake pedal supports, and clutch and transmission housings. Fasteners that are
specially designed using nylon or plastic washers, sleeves, and so on, are used to
help control galvanic corrosion of magnesium [9].
22.4 SUMMARY
Limitations in the use of magnesium alloys for structural parts are as follows:
1. Sensitivity to stress-corrosion cracking in moist air.

2. Tendency of magnesium and its alloys to corrode when galvanically
coupled to other metals. Aluminum alloys containing some magnesium
(e.g., types 5050, 5052, and 5056) are least affected by alkalies generated
by a magnesium–aluminum couple and, hence, can be applied in contact
with magnesium. Pure aluminum is also satisfactory. In general, however,
magnesium must be insulated from all dissimilar metals; insulating washers
must be used under bolt or screw heads in order to extend the path of
electrolyte resistance and thereby minimize galvanic action.
Magnesium, in brief, is resistant to the following:
1. Atmospheric exposure. The controlled purity 3% Al, 1.5% Zn–Mg alloy

exposed for eight years to the tropical marine atmosphere at Panama lost
2.4 mm (0.094 in.) per year, compared to 0.1 mm (0.004 in.) per year in the
temperate marine atmosphere of Kure Beach, North Carolina [13]. Most
alloys must be stress relieved, avoiding subsequent high applied stress in
order to avoid stress-corrosion cracking in moist atmospheres.
2. Distilled water (same precautions as for 1).
3. >2% HF. A protective film of magnesium fluoride forms. Pitting may occur
at the water–air interface. The corrosion rate of 8% Al, 0.2% Mn alloy in
5% HF is 2.3 gmd; in 48% HF, it is 0.05 gmd.
4. Alkalies. Unlike aluminum, magnesium is resistant to alkalies. The rate in
48% NaOH−4% NaCl is 0.2 gmd (high-purity Mg). Above 60°C (140°F),
the rate increases appreciably.
Magnesium is not resistant to the following:
1. Waters containing traces of heavy metal ions.

2. Seawater.
3. Inorganic or organic acids and acid salts (e.g., NH4 salts).
4. Methanol (anhydrous); magnesium methylate forms. The reaction can be
inhibited by (NH4)2S, H2CrO4, turpentine, or dimethylglyoxime (DMG).
The higher alcohols are resisted satisfactorily.
5. Leaded gasoline mixtures.
6. Freon (CCl2F2) plus water. The anhydrous gas is not corrosive.
REFERENCES
1. E. Ghali, Magnesium and magnesium alloys, in Uhlig’s Corrosion Handbook, 2nd

edition, R. W. Revie, editor, Wiley, New York, 2000, p. 793.
2. B. A. Shaw and R. C. Wolfe, Corrosion of magnesium and magnesium-base alloys, in
ASM Handbook, Vol. 13B, Corrosion: Materials, ASM International, Materials Park,
OH, 2003, p. 205.
3. J. Hanawalt, C. Nelson, and J. Peloubet, Min. Metall. Eng., Inst. Metals Div. 147, 273
(1942).
4. H. Robinson and P. George, Corrosion 10, 182 (1954).
5. Ref. 1, p. 796.
6. B. A. Shaw, Corrosion resistance of magnesium alloys, in ASM Handbook, Vol. 13A,
OH, 2003, p. 693.
7. Ref. 1, p. 813.
8. W. K. Miller, Stress-corrosion cracking of magnesium alloys, in Stress-Corrosion Crack-
ing, R. H. Jones, editor, ASM International, Materials Park, OH, 1992, pp. 251–263.
9. D. L. Hawke and T. Ruden, Galvanic compatibility of coated steel fasteners with mag-
nesium, paper no. 950429, International Congress and Exposition, Detroit, Michigan,
SAE International, Warrendale, PA, 1995.
10. Ref. 2, pp. 218–219.
11. E. Emley, Principles of Magnesium Technology, Pergamon Press, New York, 1966, pp.
692–705.
12. Ref. 2, pp. 222–223.
13. C. Southwell, A. Alexander, and C. Hummer, Jr., Mater. Prot. 4(12), 30 (1965).
GENERAL REFERENCES
M. M. Avedesian and H. Baker, editors, Magnesium and Magnesium Alloys, ASM Specialty
Handbook, ASM International, Materials Park, OH, 1999.
E. Ghali, Magnesium and magnesium alloys, in Uhlig’s Corrosion Handbook, 2nd edition,
R. Hodkinson and J. Fenton, Lightweight Electric/Hybrid Vehicle Design, SAE International,

Butterworth-Heinemann, Oxford, 2001.
Alan A. Luo, editor, Magnesium Technology 2004, TMS, Warrendale, PA, 2004.
W. K. Miller, Stress-corrosion cracking of magnesium alloys, in Stress-Corrosion Cracking,
R. H. Jones, editor, ASM International, Materials Park, OH, 1992, pp. 251–263.
N. R. Neelameggham, H. I. Kaplan, and B. R. Powell, Magnesium Technology 2005, TMS,
Warrendale, PA, 2005.
M. O. Pekguleryuz and L. W. F. Mackenzie, Magnesium Technology in the Global Age, Cana-
dian Institute of Mining, Metallurgy and Petroleum, Montreal, Canada, 2006.
B. A. Shaw, Corrosion resistance of magnesium alloys, in ASM Handbook, Vol. 13A, Cor-
rosion: Fundamentals, Testing, and Protection, ASM International, Materials Park, OH,
2003, pp. 692–696.
23
NICKEL AND NICKEL ALLOYS
23.1 INTRODUCTION
Nickel has many applications in industry where corrosion resistance is required.

Nickel is an excellent base on which to design alloys because, first, the element
itself is moderately corrosion resistant, and, second, it can be alloyed with many
other elements while maintaining its ductile face-centered-cubic structure. As a
result, over the past 100 years, a wide range of binary, ternary, and other nickel-
base alloys were developed to meet the increasingly demanding requirements in
many industries for resistance to aqueous corrosion and to high-temperature
oxidation conditions. These new nickel-base alloys were designed by developing
and applying fundamental knowledge on the role of individual alloying elements
and by improving thermomechanical processes to optimize alloy metallurgy.
Today, nickel-base alloys are used in chemical process, petrochemical, pulp and
paper, energy conversion, power production, supercritical water, waste incinera-
tion, pharmaceutical, and many other industries. Alloy selection from the large
number of alloys available depends on the specific properties that are required.
Tables 23.1 and 23.2 list the major alloying elements and the effects that they
have on properties of alloys intended for aqueous corrosion and for high-
temperature application, respectively [1].

407
408 NICKEL AND NICKEL ALLOYS
TABLE 23.1. Alloying Elements and Their Major Effects in Alloys for Aqueous
Corrosion Resistance
Alloying Main Features Other Features
Element
Ni Provides matrix for metallurgical Enhances corrosion resistance in

compatibility with alloying mild reducing media and in alkali
elements. Improves thermal media. Improves chloride stress-
stability and fabricability. corrosion cracking (S.C.C.).
Cr Provides resistance to oxidizing Enhances localized corrosion
corrosive media. resistance.
Mo Provides resistance to reducing Enhances localized corrosion
(nonoxidizing) corrosive media. resistance and chloride S.C.C.
Provides solid solution
strengthening.
W Behaves similarly to Mo, but less Provides solid solution strengthening.
effective. Detrimental to thermal
stability in high Ni–Cr–Mo alloys.
N Austenitic stabilizer; economical Enhances localized corrosion
substitute for nickel. resistance, thermal stability, and
mechanical properties.
Cu Improves resistance to seawater Enhances resistance to environments
and sulfuric acid; detrimental to containing H2SO4 and HF.
thermal stability in higher
Ni–Cr–Mo alloys.
Ti, Nb, Ta Carbon stabilizer. Improves HAZ and intergranular
corrosion resistance.
Si High silicon (>4%) improves Detrimental in certain corrosive
resistance to oxidizing mineral environments.
acids, sulfuric acid, and nitric acid.
Fe Provides matrix for metallurgical Reduces cost by replacing nickel and
compatibility with various enhances scrap utilization.
alloying elements.
Because of the increased cost of these alloys compared to stainless steels,

they are used when stainless steels are not suitable or when product purity and/or
safety are critically important [1].
23.2 NICKEL
Ni 2+ + 2e − → Ni φ = −0.250 V
Nickel is active in the Emf Series with respect to hydrogen, but noble with respect
to iron. The theoretical potential–pH domains of corrosion, immunity, and pas-
sivation of nickel at 25°C are shown in Fig. 23.1 [2], which shows, for example,
NICKEL 409
TABLE 23.2. Alloying Elements and Their Major Effects in High Temperature Alloys
Alloying Main Features Other Features
Element
Cr Improves oxidation resistance; detrimental Improves sulfidation and

to nitriding and fluorination resistance carburization resistance.
Si Improves oxidation, nitriding, sulfidation Synergistically acts with
and carburizing resistance; detrimental to chromium to improve high
nonoxidizing chlorination resistance. temperature degradation.
Al Independently and synergistically with Cr Helps improve sulfidation
improves oxidation resistance; detrimental resistance; improves age
to nitriding resistance. hardening effects.
Mo Improves high temperature strength; Reduces chlorination
improves creep strength; detrimental to resistance.
oxidation resistance at higher temperatures.
W Similar to molybdenum.
Nb Increases short-term creep strength; may be
beneficial in carburizing; detrimental to
nitriding resistance.
C Improves strength; helps nitriding resistance;
beneficial to carburization resistance;
oxidation resistance adversely affected.
Ti Improves strengthening by age hardening. Detrimental to nitriding
resistance.
Mn Slight positive effect on high temperature
strength and creep; detrimental to
oxidation resistance; increases solubility of
nitrogen.
Co Reduces rate of sulfur diffusion; hence, Increases solubility of
improves sulfidation resistance; improves carbon in nickel-base
solid solution strength. alloys, increasing resistance
to carburization.
Ni Improves carburization, nitriding, and
chlorination resistance; detrimental to
sulfidation resistance.
Y, Re Improves adherence and spalling resistance
of oxide layer, and hence, improves
oxidation, sulfidation, carburization
resistance.
that nickel can be cathodically protected in acid or neutral solution by controlling

the potential below about −0.4 V versus S.H.E.
Nickel does not react rapidly with dilute nonoxidizing acids (e.g., H2SO4 and
HCl) unless dissolved oxygen is present. It is thermodynamically inert to (will
not corrode in) deaerated water at room temperature, in which Ni(OH)2 forms
as a corrosion product. It is passive in contact with many aerated aqueous solu-
tions, but the passive film is not as stable as, for example, that on chromium (for
nickel at 25°C [2]. (M. Pourbaix, Atlas of Electrochemical Equilibria in Aqueous Solutions, 2nd
English edition, p. 334. Copyright ANCE International 1974 and CEBELCOR.)
nickel, Flade potential φF = 0.2 V ) [3]. It corrodes by pitting when exposed to
seawater (passive–active cells).
Nickel is outstandingly resistant to hot or cold alkalies. Only silver and
possibly zirconium are more resistant. Nickel exposed to boiling 50% NaOH
corrodes at the rate of 0.06 gmd (0.0001 ipy). It also resists fused NaOH, low-
carbon nickel being preferred for this application in order to avoid intergranular
attack of the stressed metal; stress relief anneal, 5 min at 875°C (1100°F) is advis-
able. Nickel is attacked by aerated aqueous ammonia solutions, a soluble complex,
Ni(NH 3)62+ , forming as a corrosion product. It is also attacked by strong hypo-
chlorite solutions with formation of pits.
Nickel is not subject to stress-corrosion cracking except in high concentra-
tions of alkali or in fused alkali.
Nickel has excellent resistance to oxidation in air up to 800–875°C (1500–
1600°F) and is often used in service at still higher temperatures. When subject to
alternate oxidizing and reducing atmospheres at elevated temperatures, it tends
to oxidize along grain boundaries. It also fails along grain boundaries in the pres-
ence of sulfur-containing environments above about 315°C (600°F). Fused salts
contaminated with sulfur, or with sulfates in the presence of organic or other
chemically reducing impurities, may damage nickel or high-nickel alloys in this
manner.
NICKEL ALLOYS 411
In summary, nickel is resistant to the following:
1. Alkalies, hot or cold, including fused alkalies.

2. Dilute nonoxiding inorganic and organic acids. Resistance is improved if
acids are deaerated.
3. The atmosphere. In industrial atmospheres, a nonprotective film forms,
composed of basic nickel sulfate (fogging). Fogging is minimized by a thin
chromium electroplate over nickel. There is good resistance to oxidation
in air at elevated temperatures.
Nickel is not resistant to the following:
1. Oxidizing acids (e.g., HNO3).

2. Oxidizing salts (e.g., FeCl3, CuCl2, and K2Cr2O7).
3. Aerated ammonium hydroxide.
4. Alkaline hypochlorites.
5. Seawater.
6. Sulfur or sulfur-containing reducing environments, >315°C (>600°F).
23.3 NICKEL ALLOYS
23.3.1 General Behavior

Adding copper to nickel improves, to a moderate degree, resistance under
reducing conditions (e.g., nonoxidizing acids, including hydrofluoric acid). Also,
in line with the resistance of copper to pitting, the tendency of nickel–copper
alloys to form pits in seawater is less pronounced than for nickel, and pits tend
to be shallow rather than deep. Above about 60–70 at.% Cu (62–72 wt.% Cu),
the alloys lose the passive characteristics of nickel and tend to behave more
like copper (see Section 6.8.1) retaining, however, appreciably improved resis-
tance to impingement attack. Hence, 10–30% Ni, bal. Cu alloys (cupro-nickels)
do not pit in stagnant seawater and are resistant to corrosion in rapidly flowing
seawater. Such alloys containing a few tenths to 1.75% Fe, which still further
improves resistance to impingement attack, are used for seawater condenser
tubes. The 70% Ni–Cu alloy (Monel), on the other hand, pits in stagnant sea-
water and, in seawater, is best used under rapidly moving, aerated conditions
that ensure uniform passivity. It does not pit under conditions that provide
cathodic protection, such as when the alloy is coupled to a more active metal
(e.g., iron).
Additions of chromium to nickel impart resistance to oxidizing conditions
(e.g., HNO3 and H2CrO4) by supporting the passivation process. The critical
minimum chromium content [4] obtained from critical current densities for
anodic passivation in sulfuric acid is 14 wt.% Cr. These alloys are more sensitive
than nickel to attack by Cl− and by HCl, and deep pits form when the alloys are
exposed to stagnant seawater. Chromium also imparts to nickel improved resis-

tance to oxidation at elevated temperatures. One important commercial alloy
contains 20% Cr, 80% Ni (see Section 11.13.4).
Alloying nickel with molybdenum provides, to a marked degree, improved
resistance under reducing conditions, such as in hydrochloric acid. The corrosion
potentials of such alloys in acids, whether aerated or deaerated, tend to be more
active than their Flade potentials [5]; hence, the alloys are not passive in the sense
of Definition 1 (Section 6.1). For example, the corrosion potentials of nickel alloys
containing 3–22.8% Mo in 5% H2SO4, hydrogen-saturated, all lie within 2 mV
of a platinized platinum electrode in the same solution [5]. Notwithstanding an
active corrosion potential, the alloy containing 15% Mo, for example, corrodes
at 1/12 the rate of nickel in deaerated 10% HCl at 70°C, and the rate decreases
still further with increasing molybdenum content (1/100 the rate for nickel at
25% Mo). Polarization measurements show that molybdenum alloyed with nickel
has little effect on hydrogen overpotential, but increases anodic polarization
instead; hence, the corrosion rate of the alloy is anodically controlled. The mecha-
nism of increased anodic polarization is related most likely to a sluggish hydra-
tion of metal ions imparted by molybdenum, or alternatively to a porous
diffusion-barrier film of molybdenum oxide, rather than to formation of a passive
film typical of chromium or the passive chromium–nickel alloys.
As an alloying element in nickel, tungsten behaves similarly to molybdenum,
but is less effective [6].
Because the binary nickel–molybdenum alloys have poor physical properties
(low ductility, poor workability), other elements, for example, iron, are added to
form ternary or multicomponent alloys. These are also difficult to work, but they
mark an improvement over the binary alloys. Resistance of such alloys to hydro-
chloric and sulfuric acids is better than that of nickel, but it is not improved with
respect to oxidizing media (e.g., HNO3). Since the Ni–Mo–Fe alloys have active
corrosion potentials and do not, therefore, establish passive–active cells, they do
not pit in the strong acid media to which they are usually exposed in practice.
By alloying nickel with both molybdenum and chromium, an alloy is obtained
resistant to oxidizing media imparted by alloyed chromium, as well as to reducing
media imparted by molybdenum. One such alloy, which also contains a few
percent iron and tungsten (Alloy C), is immune to pitting and crevice corrosion
in seawater (10-year exposure) and does not tarnish appreciably when exposed
to marine atmospheres. Alloys of this kind, however, despite improved resistance
to Cl−, corrode more rapidly in hydrochloric acid than do the nickel–molybdenum
alloys that do not contain chromium.
Nominal compositions of some commercial nickel-base alloys containing
copper, molybdenum, or chromium are given in Table 23.3. The Ni–Cu alloys are
readily rolled and fabricated, whereas the Ni–Cr alloys are less readily, and the
Ni–Mo–Fe and Ni–Mo–Cr alloys are difficult to work or fabricate.
Some commercial Cr–Ni–Fe–Mo alloys corresponding in composition to
high-nickel stainless steels also contain a few percent copper. They are designed
to resist, among other media, sulfuric acid over a wide range of concentrations.
TABLE 23.3. Typical Compositions (%) of Commercial Nickel-Base Alloys
Alloy Common UNS Ni Mo Coa Cr W Fe Sia Mna Ca Other

NICKEL ALLOYS
System Name of No.

Alloy
Ni–Cu 400 N04400 66.5 — — — — 2.5a 0.5 0.2 0.3 Cu: 31.5
a
Ni–Cr 625 N06625 61 9 1.0 21.5 — 5.0 0.5 0.5 0.1 Nb + Ta: 3.6
Al: 0.4; Ti: 0.4
Ni–Mo B N10001 Bal. 29.5 2.5 1.0a — 6.0a 1.0 1.0 0.12
B-2 N10665 Bal. 28 1.0 1.0a 0.5a 2.0a 0.1 1.0 0.02 Cu: 0.5a
B-3 N10675 65b 28.5 3.0 1.5 3.0a 1.5 0.1 3.0 0.01 Cu: 0.2a; Al: 0.5a
Ni–Cr–Fe 600 N06600 Bal. — — 15.5 — 8 0.5 0.5 0.15 Cu: 0.2
800H N08810 32 — — 21 — Bal. 0.5 0.08 Al: 0.4; Ti: 0.38
690 N06690 58.0b — — 30 — 10 0.5 0.5 0.05 Cu: 0.5a
a
Ni–Cr–Fe– G N06007 Bal. 6.5 2.5 22.0 1.0 19.5 1.0 2.0 0.05 Cu: 2.0; Nb: 2.0
Mo–Cu G-3 N06985 Bal. 7 5.0 22.0 1.5a 19.5 1.0 1.0 0.015 Cu: 2.0
Ni–Cr–Mo C N10002 Bal. 16 2.5 16 4 6 1.0 1.0 0.08 V: 0.35a
C-22 N06022 Bal 13 2.5 22 3 3 0.08 0.5 0.015 V: 0.35a
C-276 N10276 Bal. 16 2.5 16 4 5 0.08 1.0 0.02 V: 0.35a
59 N06059 Bal. 16 — 23 — 1.5a 0.1 0.5 0.01 Al: 0.25
Ni–Fe–Cr 825 N08825 42 3 — 21.5 — 22.0b 0.2 0.5 0.05 Al: 0.2a; Ti: 0.9
a
Maximum. bMinimum.
Source: Adapted from Metals Handbook, Desk Edition, 2nd edition, ASM International, Materials Park, OH, 1998, p. 610.
For detailed alloy specifications, see, for example, Worldwide Guide to Equivalent Nonferrous Metals and Alloys, 4th edition, ASM International, Materials
Park, OH, 2001.
413
The function of alloyed copper is the same as that of alloyed palladium in tita-
nium mentioned in Section 6.4, namely, to accelerate the cathodic reaction (H+
or O2 reduction) to the point where the anodic current density reaches or exceeds
the critical value for anodic passivation.
23.3.2 Ni–Cu System: Alloy 400—70% Ni, 30% Cu

Because nickel and copper in all proportions form solid solutions, many nickel–
copper and copper–nickel alloys are possible. The first commercial nickel–copper
alloy was Alloy 400 (commonly known as Monel), which is still widely used today.
With about 31% copper in a nickel matrix, its corrosion behavior is similar to that
of nickel in many ways, but improved relative to nickel in other ways [7]. Since
Alloy 400 is resistant to high-velocity seawater, it is often used for valve trim and
pump shafts. It is also used for industrial hot freshwater tanks and for equipment
in the chemical industry. It resists boiling sulfuric acid in concentrations less than
20%, with the corrosion rate being <0.20 mm/y (<0.008 ipy)(23-h test) [8]. It is
outstandingly resistant to unaerated HF at all concentrations and temperatures
up to boiling. [Rate in N2-saturated 35% HF, 120°C (248°F) is 0.025 mm/y
(0.001 ipy); when air saturated, 3.8 mm/y (0.15 ipy) [9].] Resistance to alkalies is
good, except in hot concentrated caustic solutions or aerated NH4OH.
Alloy 400 is not resistant to oxidizing media (e.g., HNO3, FeCl3, CuSO4, and
H2CrO4) nor to wet Cl2, Br2, SO2, and NH3. The alloy is susceptible to S.C.C. in
moist aerated hydrofluoric acid and in hydrofluorosilicic acid vapor, but suscep-
tibility can be minimized by deaeration of the environment and by stress relief
annealing the alloy component [10].
23.3.3 Ni–Cr–Fe System: Alloy 600—76% Ni, 16% Cr, 7% Fe

Alloy 600 resists oxidizing aqueous media [e.g., mine waters, Fe2(SO4)3, CuSO4,
and HNO3]. In nitric acid, resistance is best above 20% HNO3, including red
fuming acid, but is not as good, in general, as the stainless steels. Resistance to
alkalies is good, except in concentrated hot caustic solutions. It is also resistant
to all concentrations of NH4OH at room temperature. Like the stainless steels,
this alloy tends to pit in seawater and also in oxidizing metal chlorides, such as
FeCl3.
Alloy 600 is used extensively where oxidation resistance at elevated tempera-
tures is required (see Section 11.13.4).
Pressurized water reactors of nuclear-power plants use mill-annealed Alloy
600 tubes for heat exchangers. Typically, reactor coolant circulates through the
tubes at 315°C (600°F) exiting 30–35°C lower in temperature. Boiler water in
contact with the outside of the tubes is all-volatile treated (minimum dissolved
solids and dissolved O2, slightly alkaline using NH3). Thinning and intergranular
S.C.C. of tubes tend to occur at inlet-end sections above the tube sheet in crevice
and sludge buildup areas [11]. Washings from such areas test alkaline and are
high in sodium. Hence, laboratory tests of stressed alloy exposed to hot NaOH
NICKEL ALLOYS 415
solutions (290–365°C) are used as an accelerated measure of resistance to S.C.C.

in operational steam units. Such tests show that heat treatment of Alloy 600 at
either 650°C for 4 h or at 700°C for 16 h or more considerably improves resistance
to S.C.C. in NaOH solutions [12]. The improved resistance also extends to an
environment of relatively pure water at 345°C (650°F) [12]. Through heat treat-
ment, discontinuous carbide precipitates form at grain boundaries accompanied
at 650°C (but not at 700°C) by chromium depletion. The latter situation accounts
for intergranular corrosion of the alloy by 25% HNO3 and by polythionic acids.
But whether or not chromium depletion occurs is not related to the cause of
intergranular S.C.C.
Accordingly, Alloy 600 fails in 10% NaOH at 315°C (600°F) independent of
carbon content (0.006–0.046%) [13]; and an alloy (18% Cr, 77% Ni) approximat-
ing the Alloy 600 composition, but containing only 0.002% C, remains susceptible
in water at 350°C (660°F) [14]. The long incubation time typically required for
cracks to initiate in pure water (several months) supports the view that specifi-
cally damaging elements must reach a critical concentration by slow diffusion to
grain boundaries in order for the alloy to become susceptible. Both phosphorus
and boron have been suspected [13, 15] (see also Section 19.2.3.3). Alloy 690,
however, has been found to provide satisfactory service, with no reported failures
by intergranular S.C.C. [16].
Alloy 600 is resistant to S.C.C. in boiling MgCl2 solutions. The extent of S.C.C.
of the alloy in water at 350°C is unaffected by, and remains intergranular in, the
presence of 0.1% NaCl [14].
23.3.4 Ni–Mo System: Alloy B—60% Ni, 30% Mo, 5% Fe

The original Alloy B (N10001) was invented in the 1920s. Alloy B and commercial
alloys of similar composition are resistant to hydrochloric acid of all concentra-
tions and temperatures up to the boiling point. The rate of corrosion is 0.23 mm/y
(0.009 ipy) in boiling 10% HCl; 0.5 mm/y (0.02 ipy) in boiling 20% HCl; and
0.05 mm/y (0.002 ipy) in 37% HCl at 65°C (150°F) [17]. Resistance to boiling
sulfuric acid is good up to 60% H2SO4 (<0.2 mm/y, <0.007 ipy). In phosphoric acid,
rate of attack is low for all concentrations and temperatures, with the highest
rate for the pure acid applying to the boiling 86% H3PO4 (0.8 mm/y, 0.03 ipy). In
various organic acids, hot or cold, resistance is also good.
Because of the lack of chromium, Alloy B is not resistant to oxidizing condi-
tions (for example, HNO3) or to oxidizing metal chlorides (such as FeCl3) [18].
Contamination of nonoxidizing acids with oxidizing ions (such as Fe3+ or Cu2+)
causes a large increase in corrosion rate [19]. Nickel–molybdenum alloys must
not be used where oxidizing conditions exist.
Because of the high carbon content of Alloy B, it is subject to intergranular
attack in nonoxidizing acids (e.g., acetic, formic, and hydrochloric) when heated
in the range 500–700°C (930–1300°F), as may occur in the heat-affected zone
(HAZ) of a weld. Heat treatment to avoid such attack consists of annealing
at 1150–1175°C (2100–2150°F), followed by rapid cooling in air or water. The
low-carbon alloy, B-2, is less susceptible to intergranular attack and HAZ corro-
sion, but it is difficult to fabricate and can crack during manufacturing operations.
These embrittlement problems were resolved by developing Alloy B-3, with care-
fully controlled additions of iron, chromium, and manganese [18, 19].
23.3.5 Ni–Cr–Fe–Mo–Cu System: Alloy G—Ni, 22% Cr, 20% Fe,

6.5% Mo, 2% Cu
The high nickel content in these alloys provides corrosion resistance in reducing
environments. The chromium content contributes to strength, aqueous corrosion
resistance in oxidizing environments, and oxidation resistance. Alloy G was
developed during the 1960s. Alloy G-3 is an improvement on Alloy G, but with
greater resistance to HAZ attack and better weldability. The lower carbon content
results in slower kinetics of carbide precipitation, and the higher molybdenum
content improves the localized corrosion resistance. As a result, Alloy G-3 has
replaced Alloy G in most applications. Alloy G-3 is widely used for downhole
tubulars in the oil and gas industry [20, 21].
23.3.6 Ni–Cr–Mo System: Alloy C—54% Ni, 15% Cr, 16% Mo,
4% W, 5% Fe
The Ni–Cr–Mo alloys are widely used within the chemical process industry.
These alloys are resistant to both oxidizing and reducing environments. They
resist chloride-induced pitting, crevice corrosion, and S.C.C. In addition, they are
easily formed and are weldable.
Because of its chromium content, Alloy C is resistant to such oxidizing media
as HNO3, HNO3–H2SO4 mixed acids, H2CrO4, Fe2(SO4)3, FeCl3, and CuCl2. Cor-
rosion rates fall below 0.5 mm/y (0.02 ipy) in <50% HNO3 at 65°C (150°F), but
are higher above this concentration. In boiling >15% HNO3, rates are high.
Resistance is excellent to wet or dry Cl2 at room temperature; pitting in wet Cl2
may occur at higher temperatures. Alloy C also resists wet or dry SO2 up to about
70°C (155°F)[17]. Alloy C has outstanding resistance to pitting or crevice corro-
sion in seawater. Resistance to acetic acid is excellent. In boiling 40% formic acid,
the rate is 0.25 mm/y (0.01 ipy).
Alloy C has good resistance to hydrochloric acid at room temperature
[0.025 mm/y (0.001 ipy) for 37% HCl], but not at higher temperatures [5 mm/y
(0.2 ipy) for 20% HCl, 65°C (150°F)]. It is recommended for boiling sulfuric acid
up to 10% acid (0.25 mm/y) and for boiling phosphoric acid up to at least 50%
acid (0.25 mm/y).
When heated in the temperature range 500–700°C (930–1300°F), the alloy
tends to corrode intergranularly; for this reason, weld HAZs undergo severe
intergranular corrosion, which can be avoided by a final heat treatment at 1210–
1240°C (2210–2260°F), followed by rapid cooling in air or water [22].
Alloy C-276, introduced in the 1960s, contains less carbon and is less sensitive
to intergranular corrosion resulting from intermediate heat treatment. For this
REFERENCES 417
reason, Alloy C-276 can be used in most applications in the as-welded condition
without severe intergranular attack.
Alloy C-22 and Alloy 59 were developed for applications where resistance
to corrosion under highly oxidizing conditions is required. The high chromium
content in these alloys, 22% and 23% for C-22 and 59, respectively, imparts excel-
lent corrosion resistance of these alloys to nitric acid [23]. In addition, these alloys
have been found to have superior crevice corrosion resistance in seawater [24].
23.3.7 Ni–Fe–Cr System: Alloy 825—Ni, 31% Fe, 22% Cr

The Ni–Fe–Cr system bridges the gap between the high-nickel austenitic stainless
steels and the Ni–Cr–Fe alloy system. Alloy 825 is an upgrade from the 300 series
stainless steels and is used to obtain resistance to localized corrosion and S.C.C.
This alloy was developed from Alloy 800 by increasing the nickel content and by
adding molybdenum (3%), copper (2%), and titanium (0.9%) for improved cor-
rosion resistance in many media [20, 21].
REFERENCES
1. D. C. Agarwal, Nickel and nickel alloys, in Uhlig’s Corrosion Handbook, 2nd edition,
R. W. Revie, editor, Wiley, New York, 2000, p. 831.
2. M. Pourbaix, Atlas of Electrochemical Equilibria in Aqueous Solutions, National Asso-
ciation of Corrosion Engineers, Houston, TX, and CEBELCOR, Brussels, 1974,
p. 334.
3. J. Osterwald and H. Uhlig, J. Electrochem. Soc. 106, 515 (1961).
4. P. Bond and H. Uhlig, J. Electrochem. Soc. 107, 488 (1960).
5. H. Uhlig, P. Bond, and H. Feller, J. Electrochem. Soc. 110, 650 (1963).
6. Ref. 1, p. 834.
7. Ibid., p. 835.
8. W. Z. Friend, in Corrosion Handbook, H. H. Uhlig, editor, Wiley, New York, 1948,
p. 271.
9. Ibid., p. 273.
10. Ref. 1, p. 836.
11. G. Airey and F. Pement, Corrosion 39, 46 (1983).
12. H. Domian et al., Corrosion, 33, 26 (1977).
13. J. Crum, Corrosion 38, 40 (1982).
14. H. Coriou et al., in Proceedings of Conference Fundamental Aspects of Stress Corro-
sion Cracking, R. Staehle et al., editor, National Association of Corrosion Engineers,
Houston, TX, 1969, p. 352.
15. N. Pessall et al., Corrosion 35, 100 (1979).
16. P. M. Scott and P. Combrade, Corrosion in pressurized water reactors, in ASM Hand-
book, Vol. 13C, Corrosion: Environments and Industries, ASM International, Materials
Park, OH, 2006, pp. 367, 369.
17. Manufacturer’s literature.

18. Ref. 1, p. 837.
19. P. Crook, Corrosion of nickel and nickel-base alloys, in ASM Handbook, Vol. 13B,
20. Ref. 1, p. 840.
21. Ref. 19, p. 231.
22. C. Samans, A. Meyer, and G. Tisinai, Corrosion 22, 336 (1966).
23. Ref. 19, p. 236.
24. Ref. 19, p. 238.
GENERAL REFERENCES
D. C. Agarwal, Nickel and nickel alloys, in Uhlig’s Corrosion Handbook, 2nd edition,
P. Crook, Corrosion of nickel and nickel-base alloys, in ASM Handbook, Vol. 13B, Corro-
sion: Materials, ASM International, Materials Park, OH, 2005, pp. 228–251.
A. J. Sedriks, Corrosion resistance of stainless steels and nickel alloys, in ASM Handbook,
als Park, OH, 2006, pp. 697–702.
Corrosion in the Nuclear Industry

B. M. Gordon, Introduction to corrosion in the nuclear power industry, in ASM Handbook,
Vol. 13C, Corrosion: Environments and Industries, ASM International, Materials Park,
OH, 2006, pp. 339–340.
F. P. Ford, B. M. Gordon, and R. M. Horn, Corrosion in boiling water reactors, in ASM
P. M. Scott and P. Combrade, Corrosion in pressurized water reactors, in ASM Handbook,
Vol. 13C, Corrosion: Environments and Industries, ASM International, Materials Park,
OH, 2006, pp. 362–385.
G. Was, J. Busby, and P. L. andresen, Effect of irradiation on stress-corrosion cracking and
corrosion in light water reactors, in ASM Handbook, Vol. 13C, Corrosion: Environ-
ments and Industries, ASM International, Materials Park, OH, 2006. pp. 386–414.
Environmental Degradation of Materials in Nuclear Power Systems—Water Reactors,
Proceedings, Eighth International Symposium, American Nuclear Society, La Grange
Park, IL, 1997.
24
COBALT AND COBALT ALLOYS
24.1 INTRODUCTION
Co2+ + 2e − → Co φ = −0.277 V
The standard potential of cobalt is close to that of nickel, being 27 mV more

active (Table 3.2, Section 3.8). Like nickel, the metal is rapidly attacked by
oxidizing acids and salts (for example, HNO3 and FeCl3); it resists alkalies,
hot or cold, although not as well as does nickel. Cobalt is also corroded by
aerated aqueous ammonia solutions, forming a soluble complex—for example,
Co(NH 3)62+ .
The theoretical potential–pH domains of corrosion, immunity, and passiv-
ation of cobalt in aqueous solution are presented in Fig. 24.1 [1]. As this figure
indicates, cobalt can be cathodically protected in acid or neutral solution by
polarizing to potentials active to −0.5 V versus S.H.E. [1].
At elevated temperatures, cobalt is relatively resistant to oxidation in air. It
resists hot reducing sulfur-bearing atmospheres better than nickel does.

419
420 COBALT AND COBALT ALLOYS
Figure 24.1. Theoretical potential–pH domains of corrosion, immunity, and passivation of

cobalt at 25°C [1]. (M. Pourbaix, Atlas of Electrochemical Equilibria in Aqueous Solutions, 2nd
English edition, p. 326. Copyright NACE International 1974 and CEBELCOR.)
24.2 COBALT ALLOYS
Being less plentiful and more expensive than nickel, cobalt is usually alloyed with
chromium for applications where the alloys have practical advantages over
similar nickel- or iron-base alloys. The cobalt-base alloys, for example, are better
resistant to fretting corrosion, to erosion by high-velocity liquids, and to cavita-
tion damage.
Chromium-bearing cobalt alloys can be divided into three groups [2]:
1. Alloys for wear resistance

2. Alloys for high-temperature use
3. Alloys for resistance to aqueous corrosion and wear
Cobalt alloys were developed in the early 1900s by Elwood Haynes of

Kokomo, Indiana, for resisting corrosive environments and for high-temperature
strength and hardness. The alloys are used in cutting tools operating in aggressive
chemical media, steam valves and valve seats, pressure gauges, bushings, nozzles,
pressure seats, and implant materials for the human body.
At temperatures up to 417°C, cobalt has a hexagonal close packed (hcp)
structure, whereas above 417°C, it is face-centered cubic (fcc). Alloying elements
that are fcc stabilizers (such as nickel, iron, and carbon) lower the transformation
COBALT ALLOYS 421
temperature. On the other hand, chromium, molybdenum, and tungsten, hcp

stabilizers, raise the transformation temperature. Alloys of cobalt that contain
both fcc and hcp stabilizers have transformation temperatures that are a complex
function of the alloy composition [3]. Applying stress to alloys in a metastable
fcc structure at ambient temperature can partially transform them to hcp.
Cobalt can be anodically passivated in 1N H2SO4, with the required minimum
current density of 5000 A/m2 (500 mA/cm2) being 14 times higher than that for
nickel [4]. Alloying cobalt with chromium reduces the current density, with the
10% Cr alloy requiring only 10 A/m2 (1 mA/cm2) to become passive. The alloy
containing 10–12% Cr is negligibly attacked by 10% HNO3, hot or cold; but in
10% H2SO4 or HCl, passivity is lost, and corrosion rates become excessively high.
Alloying of Co–Cr alloys with molybdenum or tungsten reduces attack by H2SO4
or HCl, but not by HNO3.
Some commercial cobalt-alloy compositions are listed in Table 24.1. They
typically contain chromium as well as molybdenum and/or tungsten, making
them relatively resistant to both reducing and oxidizing conditions. High resis-
tance to abrasion results from the precipitation of carbides, which can be carbides
of chromium, molybdenum, and tungsten [3].
The alloys resist pitting in FeCl3 at room temperature, except Alloy 6B
because of its high carbon content of 1.2%. At a lower carbon content—for
example, 0.4%—the alloy is resistant. Vitallium, having a very noble critical
pitting potential is also resistant to pitting in dilute NaCl solutions, a property
that extends to Alloy 25 and MP35N as well.
Substantial additions of cobalt to chromium plus molybdenum (or tungsten)
alloys are detrimental to S.C.C. behavior, resembling the effect of added iron
rather than the beneficial effect of added nickel. Accordingly, the MP35N alloy
resists S.C.C. in MgCl2 solution at 153–154°C, but by replacing most nickel with
cobalt (and the incidental reduction of molybdenum to 6% and increase of chro-
mium to 30%), as in Vitallium, susceptibility results [5]. Alloy 25 is also suscep-
tible. This susceptibility does not include Vitallium exposed to saline solutions
at 37°C (body temperature) in which the alloy is resistant. The situation is analo-
gous to the observed resistance of 18–8 (types 304 and 316) stainless steels to
S.C.C. in aerated chlorides at temperatures below 60–80°C, but not above.
In boiling 50% NaOH, all of the stressed cobalt alloys fail by S.C.C., or
sometimes by relatively rapid uniform dissolution. When severely cold-worked
and cathodically polarized at room temperature in 5% H2SO4 plus As2O3, the
stressed alloys are susceptible to failure by hydrogen cracking. Similar failures
are also expected when the alloys are coupled in the same acid to a more active
metal like iron, with the resultant galvanic action paralleling cathodic polariza-
tion. Failures in 5% NaCl–0.1% acetic acid, saturated with H2S (NACE solution
[6]), which simulates deep sour gas well environments, depend on temperature
and the prevailing uniform corrosion rate to produce hydrogen. At room tem-
perature, failures in this solution by hydrogen cracking (also sometimes called
sulfide stress cracking) usually occur only for the cold-worked alloys that are
subsequently heat-treated. This heat treatment improves strength, but may also
422
TABLE 24.1. Nominal Compositions (%) of Cobalt Alloys

Alloys for Common UNS No. Cr Mo W Ni Fe C Mn Si Co Other
Name
Wear 6B R30016 30 1.5a 4 2.5 3a 1 1.4 0.7 bal. —

resistance
High 25 R30605 20 — 15 10 3a 0.1 1.5 0.4a bal. —

temperatures
Aqueous 21 R30021 27 5.5 — 2.75 3a 0.25 1a 1a bal. B 0.007a

corrosion + MP35N R30035 20 9.75 — 35 1a 0.025a 0.15a 0.15a bal. Ti 1a
wear Ultimet R31233 26 5 2 9 3 0.06 0.8 0.3 bal. N 0.08
resistance Vitallium — 30 6 — — — 0.5a 0.75a — bal. —
a
Maximum.
Source: Data from ASM Handbook, Vol. 13B, Corrosion: Materials, ASM International, Materials Park, OH, 2005, pp. 165, 172.
COBALT AND COBALT ALLOYS
increase uniform corrosion rates in acids sufficient to generate hydrogen in

amounts necessary to induce cracking. Failure by hydrogen cracking usually
diminishes as the temperature is raised (less hydrogen enters the metal and more
escapes as gas), but chloride S.C.C. may displace hydrogen cracking as the failure
mechanism in the higher-temperature range. In this event, coupling of the alloys
to a more active metal, as in cathodic protection, prevents cracking.
The advantage of cobalt-base alloys to reduce fretting corrosion contributes
to the advantage of using Vitallium in the human body. Waterhouse [7] showed
that a Vitallium screw mounted in a metal plate in saline solution and subjected
to variable stress so as to cause slight rubbing of the screw head was damaged less
than stainless steel. Also, in laboratory cavitation-erosion tests in distilled water,
cobalt alloys exhibited superior resistance [8]. Vitallium and Alloys 6B and 25
lost only 1/3 to 1/14 the weight loss of similar specimens of nickel-base C-276 and
iron-base type 304 stainless steel. Similarly, in high-velocity (244 m/s) hot brines
common to geothermal wells, Alloy 25 and MP35N resisted corrosion-erosion
better than C-276 and much better than 26% Cr–1% Mo stainless steel [9].
REFERENCES
1. M. Pourbaix, Atlas of Electrochemical Equilibria in Aqueous Solutions, 2nd English

edition, National Association of Corrosion Engineers, Houston, TX, and CEBELCOR,
Brussels, 1974, p. 326.
2. P. Crook and W. L. Silence, Cobalt alloys, in Uhlig’s Corrosion Handbook, 2nd edition,
R. W. Revie, editor, Wiley, New York, 2000, p. 717.
3. Ref. 2, p. 718.
4. A. Bond and H. Uhlig, J. Electrochem. Soc. 107, 488 (1960).
5. H. Uhlig and A. Asphahani, Mater. Perf. 18(11), 9 (1979).
6. Standard Test Method, TM0284-2003, Evaluation of Pipeline and Pressure Vessel Steels
for Resistance to Hydrogen-Induced Cracking, NACE International, Houston, TX.
7. R. Waterhouse, Fretting Corrosion, Pergamon Press, New York, 1972, p. 59.
8. P. Crook and H. Richards, Proceedings of the Conference on Production and Applica-
tions of Less Common Metals, The Metals Society, London, 1982.
9. The LLL Geothermal Energy Program Status Report, A. Austin et al., editors,
Lawrence Livermore Laboratory, Livermore, California, April 1977.
GENERAL REFERENCES
Corrosion of cobalt and cobalt-base alloys, in ASM Handbook, Vol. 13B, Corrosion:
P. Crook and W. L. Silence, Cobalt Alloys, in Uhlig’s Corrosion Handbook, 2nd edition,
J. R. Davis, editor, Nickel, Cobalt, and Their Alloys, ASM Specialty Handbook, ASM
International, Materials Park, OH, 2000.
25
TITANIUM
25.1 TITANIUM
Ti 2+ + 2e → Ti φ = −1.63 V
Titanium is very active in the Emf Series, about 1.2 V more active than iron
(Table 3.2, Section 3.8). The theoretical potential–pH domains of corrosion,
immunity, and passivation of titanium in aqueous solution are presented in Fig.
25.1 [1]. In this figure, passivation is attributed to a film of TiO2. The excellent
corrosion resistance of titanium in many environments results from a hard, tightly
adherent oxide film that forms instantaneously in the presence of an oxygen
source [2]. This film, typically less than 10 nm thick, is very chemically resistant
and is attacked by very few substances, including hot concentrated HCl, H2SO4,
NaOH, and HF [3].
Titanium is a metal of relatively high melting point [m.p. = 1668°C (3053°F);
density = 4.5 g/cm3]. It was developed for the aircraft industry because of its high
strength-to-weight ratio and excellent corrosion resistance; it is now widely used
in chemical process equipment.
It has been reported that, in the active state, titanium may oxidize to form
Ti3+ ions in solution [4]. The metal is readily passivated in aerated aqueous

425
426 TITANIUM
Figure 25.1. Theoretical potential–pH domains of corrosion, immunity, and passivation of

titanium at 25°C, assuming passivation by TiO2 [1]. (M. Pourbaix, Atlas of Electrochemical
Equilibria in Aqueous Solutions, 2nd English edition, p. 219. Copyright NACE International
1974 and CEBELCOR.)
solutions, including dilute acids and alkalies. In the passive state, titanium is
covered with a nonstoichiometric oxide film [4], the average composition of
which is TiO2. Semiconducting properties of the passive film are generally attrib-
uted to oxygen anion vacancies and Ti3+ interstitials that function as donor states
and give n-type semiconducting characteristics to the oxide. The galvanic poten-
tial of titanium in seawater is near the noble value for stainless steels (see Fig.
3.3, Section 3.8). The Flade potential region (see Section 6.2) is relatively active
(φF ≈ −0.05 V), indicating stable passivity [5, 6]. Only in strong acids or alkalies
does passivity break down, accompanied by appreciable corrosion.
Titanium is markedly resistant to oxidizing media in the presence of Cl−, for
example, heavy metal chlorides (FeCl3), aqua regia at room temperature, or wet
chlorine. It is better resistant to nitric acid at elevated temperatures than are the
stainless steels. It resists alkalies at room temperature, but is attacked by hot
concentrated or fused sodium hydroxide. Although titanium resists attack by
hot dilute NaOH or by dilute H2O2, combining the two produces high initial
TITANIUM ALLOYS 427
TABLE 25.1. Corrosion Rates of Commercial Titanium in Alkaline-Peroxide Solutions [8]

60°C, Test Period 1.5 h gmd mm/y
% NaOH % H2O2
2 1 696 56
2 1 + 0.5% (NaPO3)6 169 14
0.5 1 + 0.5% (NaPO3)6 22 1.8
1 0.35 + 1% Na2SiO3 + 0.05% (NaPO3)6 0.0 0.0
corrosion rates of more than 50 mm/y (2 ipy) [7, 8]. Some data are given in Table
25.1, which also shows the inhibiting properties of added sodium hexametaphos-
phate and sodium silicate.
On exposure of the metal for 1 h or more, stressed or unstressed, to fuming
HNO3 containing 2.5–28% NO2 and not more than 1.25% H2O, a dark substance
forms over the surface (97.5% Ti metal by X-ray analysis) [9]. In the dry state,
this surface film is pyrophoric when scratched, and it explodes when abraded in
contact with concentrated HNO3. The 8% Mn–Ti alloy is especially sensitive in
this regard.
Titanium, presumably as sponge, in contact with liquid oxygen is reported
to be sensitive to detonation by impact [10].
25.2 TITANIUM ALLOYS
Some commonly used titanium alloys are listed in Table 25.2. Group I alloys are
the commercially pure grades, whereas Group II alloys contain palladium for
improved corrosion resistance in reducing media. Groups I and II contain a single
phase, the α phase, which has a hexagonal close-packed (hcp) structure. Groups
III, IV, and V contain increasing concentrations of alloying elements and of
the second phase, the β, body-centered cubic phase. Beta alloys are used pre-
dominantly in the aerospace industry because of their high strength/density
ratios [2].
Although corrosion resistance is poor in boiling HCl or H2SO4 (114 mm/y in
boiling 10% HCl), resistance is improved by orders of magnitude in the presence
of small amounts of Cu2+ or Fe3+ (0.15 mm/y in 10% HCl, boiling, containing 0.02
mole Cu2+ or Fe3+ per liter) [11]. Small amounts of nickel, either in the environ-
ment or alloyed with titanium, also improve corrosion resistance; for example,
0.1% Ni in titanium or 0.2 ppm Ni2+ added to the solution are reported [12] to
establish passivity in boiling 3.5% NaCl acidified to pH 1. In this solution, it is
furthermore reported that the corrosion rate is lowest for the basal plane of the
hexagonal close-packed titanium lattice. Small alloying additions of palladium,
platinum, or ruthenium also effectively reduce the corrosion rate in boiling 10%
HCl (2.5 mm/y for 0.1% Pd alloy, Fig. 25.2) [13, 14]. Ion implanting titanium
428 TITANIUM
TABLE 25.2. Some Commonly Used Titanium Alloys [2]

Common UNS Number ASTM Grade Nominal
Alloy Composition
Designation (%)
Group I Commercially Pure Titanium

Grade 2 R50400 2 0.12 O
Group II Low Alloy Content Titanium with Pd Additions

Grade 2, Pd R52400 7 0.12 O, 0.15 Pd
Grade 2, low Pd R52402 16 0.12 O, 0.05 Pd
Group III Other Alpha and Near-Alpha Alloys

Grade 12 R53400 12 0.3 Mo, 0.8 Ni
Ti 8–1–1 R54810 — 8 Al, 1 V, 1 Mo
Group IV Alpha–Beta Alloys

Ti 6–4 R56400 5 6 Al, 4 V
Group V Beta Alloys

Beta C R58640 19 3 Al, 8 V, 6 Cr,
4 Zr, 4 Mo
Figure 25.2. Corrosion of titanium in boiling 10% HCl as a function of Fe3+ and Cu2+ con-
centration and alloyed palladium or platinum.
PIT TING AND CREVICE CORROSION 429
surfaces with palladium reduces the corrosion rate [15] by a factor of 1000 in
boiling 1 M H2SO4; surface alloying with palladium by an electrospark technique
or by electrochemical deposition with subsequent annealing are similarly effec-
tive [16]. These alloying elements or oxidizing ions accelerate the cathodic reac-
tion (Cu2+, Fe3+, Ni2+ reduction, or increased rate of H+ discharge) to a level at
which the corresponding anodic current density reaches or exceeds the critical
value for anodic passivation (see Section 6.4). Anodic passivation (or anodic
protection) is also practical in HCl, H2SO4, and some other acids using a small
impressed current [17].
When titanium is cathodically polarized or coupled to a more active metal
in an acid like HCl, a surface film of titanium hydride may form. However,
because of restricted diffusion of hydrogen in titanium at room temperature,
penetration of hydrogen into the metal accompanied by metal embrittlement
occurs only above about 80°C (175°F) [18].
25.3 PITTING AND CREVICE CORROSION
Titanium is characterized by marked resistance to pitting and crevice corrosion

in seawater. Only very slight uniform weight loss occurs over periods of exposure
of several years (<0.0025 mm/y). No pitting or appreciable weight loss occurred
when titanium was buried in a variety of soils for eight years [19]. Resistance to
pitting is accounted for by a very noble critical pitting potential of about 12–14 V
in dilute chloride solutions at room temperature [20, 21]. At high Cl− concentra-
tions and elevated temperatures, the critical potential becomes much more active
(Fig. 25.3); hence, pitting corrosion is observed in hot concentrated CaCl2 and
similar solutions [22]. Addition of 1% Mo to titanium is effective in shifting the
critical potential to more noble values above 125°C (260°F), with accompanying
greater resistance to pitting in this temperature range.
Initiation of pitting in titanium is more pronounced in Br− and I− than in Cl−
solutions. The critical pitting potential in 1 M Br− and 1 M I− solutions at room
temperature are 0.9 and 1.8 V, respectively [23]. Mansfeld [24], following earlier
Russian investigations, showed that titanium loses passivity in anhydrous 1 N HCl
in CH3OH, but that passive behavior as indicated by polarization curves is
restored when >0.6% H2O is present, and that the pitting potential becomes
increasingly noble as more H2O is added.
Titanium does not undergo crevice corrosion in seawater at room tempera-
ture, but instances have been recorded in hot seawater, such as under an asbestos
gasket at 95–120°C (200–250°F) [25]. Attack of this kind, it is reported, does not
occur at temperatures below about 95°C (200°F); also, such attack is more com-
monly observed in acid and neutral rather than in alkaline chloride solutions. In
laboratory tests, Griess [26] showed that titanium undergoes crevice attack in
1 M NaCl containing dissolved oxygen at 150°C (300°F). For this type of corro-
sion, Cl− was not necessary; crevice attack was also observed in hot solutions of
I−, Br−, and SO2− 4 . Susceptibility was related to acid anodic corrosion products
430 TITANIUM
Figure 25.3. Critical pitting potentials of commercial titanium and 1% Mo–Ti alloy in 1 M
NaCl as a function of temperature [22].
accumulating in the crevice which reached a pH as low as 1.0. Hence, the 0.1%
Pd–Ti alloy, which resists breakdown of passivity in acids, was found to resist
crevice corrosion better than did titanium [26, 27]. In deaerated NaCl in which
differential aeration cells are not established, crevice corrosion is suppressed.
Various case histories of crevice and pitting corrosion observed in practice have
been described [28].
Titanium tubing can be used successfully for seawater-cooled heat exchang-
ers [29], where its resistance to pitting and corrosion-erosion make it a useful
material.
25.4 INTERGRANULAR CORROSION AND

STRESS-CORROSION CRACKING
Intergranular corrosion of titanium (and various of its alloys) occurs in fuming

nitric acid at room temperature (3- to 16-h tests). Addition of 1% NaBr acts as
an inhibitor [30]. Similar corrosion of commercially pure titanium occurs in
methanol solutions containing Br2, Cl2, or I2; or Br−, Cl−, or I− [31]. Water acts as
an inhibitor.
INTERGR ANUL AR CORROSION AND STRESS-CORROSION CR ACKING 431
The 6% Al, 4% V–Ti alloy has failed by stress-corrosion cracking (S.C.C.)

in liquid N2O4 within 40 h at 40°C (105°F) [32]. A slight excess of NO (or the
presence of H2O) inhibits such failure.
Various titanium alloys, including 8% Al, 1% Mo, 1% V–Ti (8–1–1) heated
in air in contact with moist sodium chloride (e.g., from fingerprints) at 260°C
(500°F) or higher, undergo S.C.C. (or intergranular corrosion?) usually along
grain boundaries [33–35]. Pure titanium is resistant to this type of failure.
B. F. Brown et al. [36] showed that titanium alloys in seawater, despite
otherwise excellent corrosion resistance, tend to undergo transgranular S.C.C.
when a sharp surface flaw is present. It has been observed that aqueous solu-
tions of Cl−, Br−, and I− are unique in causing S.C.C. of commercial titanium
high in oxygen content (0.2–0.4% O) and of various alloys including the 8–1–1
alloy. On the other hand, F−, SO2− − 2− − −
4 , OH , S , NO3 , and ClO4 do not cause
failure and, to the contrary, may inhibit crack propagation in some alloys sus-
ceptible to S.C.C. in distilled water (e.g., about 100 ppm KNO3 is effective) [37,
38]. Various anions of the group just listed also act as inhibitors of S.C.C. in
the presence of halide ions; in this respect, their behavior simulates the effect
of extraneous anions in the case of austenitic stainless steels (see Section
19.2.6).
Beck [38] found that cathodic polarization of the 8–1–1 alloy to −0.76 V
(S.H.E.) prevents failure in the presence of Cl−, Br−, or I−. Leckie [39] reported
protection of 7% Al, 2% Nb, 1% Ta–Ti alloy in 3% NaCl at −1.1 V (S.H.E.) and
also at −1.3 V, at which hydrogen evolution was copious. Successful anodic pro-
tection against S.C.C. of the 8–1–1 alloy was reported [38] in the presence of Cl−
but not in the presence of Br− or I−.
Failure of the 8–1–1 alloy also occurs in pure methanol (CH3OH). Interest-
ingly, adding a small amount of Cl− to distilled water or to methanol did not
increase velocity of crack propagation, but less potassium nitrate (10 ppm) was
needed to inhibit cracking in methanol as compared to water [37]. The stressed
alloy was also found to be sensitive to cracking in the pure nonaqueous solvents
CCl4 and CH2Cl2.
The 8–1–1 alloy is a mixture of mostly α (hexagonal close packed) and some
β phase (body-centered cubic), with observed cracks proceeding across grains of
the α alloy but with the β phase failing by ductile fracture. Heat-treatment pro-
cedures and composition changes (e.g., lowering the aluminum content) that
favor the β phase increase resistance to S.C.C. However, the composition of the
phase is also a determining factor, because the β phase of several other titanium
alloys is found to be susceptible to S.C.C. [40]. The sensitive effect of alloy struc-
ture, the specificity of the environment, and the effects of extraneous anions and
applied potential are similar to effects observed in the stainless steels (see Section
8.3), suggesting similarities in the mechanisms. Nevertheless, the mechanisms of
cracking of titanium alloys are still being discussed, with debate continuing to
take place regarding the relative importance of anodic dissolution and hydrogen
reduction processes.
432 TITANIUM
In brief, titanium is resistant to the following:
1. Seawater, 0.0008 mm/y, 4.5-year exposure, including high-velocity condi-

tions (0.005 mm/y, 42 m/s) [41]. Known to resist pitting and crevice attack
for five years and longer. High oxygen concentration in titanium may
induce susceptibility to S.C.C.
2. Wet chlorine (>0.9% H2O, less in flowing gas) [42]. In dry Cl2, titanium
may ignite.
3. Nitric acid, all concentrations and temperatures up to boiling, but not to
fuming HNO3.
4. Oxidizing solutions, hot or cold (e.g., CuCl2, FeCl3, CuSO4, and
K2Cr2O7).
5. Hypochlorites.
Titanium is not resistant to the following:
1. Aqueous hydrogen fluoride.
2. Fluorine.
3. Hydrochloric and sulfuric acids, except when dilute, or in moderate con-
centrations when inhibited by oxidizing metal ions (e.g., Fe3+ and Cu2+) or
other oxidizing substances (e.g., K2Cr2O7 and NaNO3) or when alloyed
with platinum or palladium.
4. Oxalic, >10% formic, anhydrous acetic [43] acids.
5. Boiling CaCl2, >55% [44].
6. Concentrated hot alkalies, or dilute alkalies plus H2O2.
7. Molten salts (e.g., NaCl, LiCl, and fluorides).
8. High-temperature exposure to air, nitrogen, or hydrogen. Oxidation in air
occurs above 450°C (840°F) with formation of titanium oxides and nitrides.
Ignition temperature decreases with increased air pressure sometimes
causing localized combustion of titanium-alloy blades in the compressor
section of gas-turbine engines [45]. Titanium hydride forms rapidly above
250°C (480°F); it forms at lower temperatures when hydrogen is cathodi-
cally discharged. Absorption of oxygen, nitrogen, or hydrogen at elevated
temperatures leads to embrittlement.
REFERENCES
1. M. Pourbaix, Atlas of Electrochemical Equilibria in Aqueous Solutions, 2nd

English edition, National Association of Corrosion Engineers, Houston, TX, and
CEBELCOR, Brussels, 1974, p. 219.
2. J. Been and J. S. Grauman, Titanium and titanium alloys, in Uhlig’s Corrosion Hand-
book, 2nd edition, R. W. Revie, editor, Wiley, New York, 2000, p. 864.
3. R. W. Schutz, Corrosion of titanium and titanium alloys, in ASM Handbook, Vol. 13B,
REFERENCES 433
4. E. J. Kelly, Modern Aspects Electrochem. 14, 319 (1982).

5. M. Stern and H. Wissenberg, J. Electrochem. Soc. 106, 755 (1959).
6. N. Thomas and K. Nobe, J. Electrochem. Soc. 116, 1748 (1969).
7. T. Fennel and N. Stalter, TAPPI, J. Tech. Assoc. Pulp and Paper Ind. 51(1), 62A
(1968).
8. T. Sigalovskaya et al., Zashchita Metallov. 12(4), 363 (1976).
9. J. Rittenhouse, Trans. Am. Soc. Metals 51, 871 (1951).
10. T.M.L. Report No. 88, Battelle Memorial Institute, Columbus, OH, November 1957;
Metals Handbook, 8th edition, Vol. 1, American Society for Metals, Cleveland, OH,
1961, p. 1152.
11. J. Cobb and H. Uhlig, J. Electrochem. Soc. 99, 13 (1952).
12. J. Green and R. Latanision, Corrosion 29, 386 (1973).
13. M. Stern and H. Wissenberg, J. Electrochem. Soc. 106, 759 (1959); M. Stern and
C. Bishop, Trans. Am. Soc. Metals 52, 239 (1960).
14. A. Sedriks, Corrosion 31, 60 (1975).
15. E. McCafferty and G. Hubler, J. Electrochem. Soc. 125, 1892 (1975).
16. N. Tomashov, G. Chernova, and T. Fedoseeva, Corrosion 36, 201 (1980).
17. J. Cotton, Chem. Ind. (London) 1958, 68.
18. L. Covington, Corrosion 35, 378 (1979).
19. B. Sanderson and M. Romanoff, Mater. Prot. 8, 29 (April 1969).
20. C. Hall, Jr., and N. Hackerman, J. Phys. Chem. 57, 262 (1953).
21. I. Dugdale and J. Cotton, Corros. Sci. 4, 397 (1964).
22. F. Posey and E. Bohlmann, Second Symposium On Fresh Water from the Sea, Athens,
Greece, May 1967.
23. T. Beck, in Localized Corrosion, R. Staehle et al., editors, National Association of
Corrosion Engineers, Houston, TX, 1974, p. 644.
24. F. Mansfeld, J. Electrochem. Soc. 118, 1412 (1971).
25. J. Jackson and W. Boyd, in Applications Related Phenomena in Titanium Alloys,
Special Technical Publication No. 432, American Society for Testing and Materials,
Philadelphia, PA, 1968, pp. 218–226. See also K. Shiobara and S. Morioka, in Proceed-
ings of the Fifth International Congress on Metallic Corrosion, National Association
of Corrosion Engineers, Houston, TX, 1974, pp. 313–317.
26. J. Griess, Jr., Corrosion 24, 96 (1968).
27. A. Takamura, Corrosion 23, 306 (1967).
28. Mater. Prot. 6(10), 22 (1967).
29. J. McMaster, Mater. Perf. 18(4), 28 (1979); K. Suzuki and Y. Nakamoto, Mater. Perf.
20(6), 23 (1981).
30. G. Kiefer and W. Harple, Metals Progr. 63, 2, 74 (1953).
31. A. Sedriks and J. Green, Corrosion 25, 324 (1969).
32. J. Jackson and W. Boyd, Corrosion of Ti, DMIC Memo 218, Battelle Memorial Insti-
tute, Columbus, OH, September 1966.
33. Stress Corrosion Cracking of Titanium, Special Technical Publication No. 397,
American Society for Testing and Materials, Philadelphia, 1966. Also S. Rideout
et al. in Ref. 40, p. 650.
434 TITANIUM
34. R. Newcomber, H. Tourkakis, and H. Turner, Corrosion 21, 307 (1965).

35. H. Gray, Corrosion 25, 337 (1969); H. Gray and J. Johnston, Metall. Trans. 1, 3101
(1970).
36. B. F. Brown et al., Marine Corrosion Studies (Third Interim Report of Progress), NRL
Memo, Report 1634, Naval Research Laboratory, Washington, D.C., July 1965.
37. T. Beck and M. Blackburn, Am. Inst. Aeronaut. Astron. J. 6, 326 (1968).
38. T. Beck, J. Electrochem. Soc. 114, 551 (1967).
39. H. Leckie, Corrosion 23, 187 (1967).
40. R. Adams and E. Von Tiesenhausen, in Proceedings of Conference Fundamental Aspects
of Stress Corrosion Cracking, R. Staehle et al., editors, National Association of Cor-
rosion Engineers, Houston, TX, 1969, p. 691.
41. T. May, International Nickel Co., private communication, 1962.
42. E. Mellway and M. Kleinman, Corrosion 23, 88 (1967).
43. K. Risch, Chem.-Ing.-Tech. 39, 385 (1967).
44. P. Gegner and W. Wilson, Corrosion 15, 341t (1959).
45. T. Strobridge et al., Report NBS 1R-79-1616, National Bureau of Standards, Boulder,
Colorado, July 1979 (Metals and Ceramic Inf. Center, CAB, June 1980, Issue No. 84,
Battelle Columbus Labs, Columbus, OH).
GENERAL REFERENCES
J. Been and J. S. Grauman, Titanium and titanium alloys, in Uhlig’s Corrosion Handbook,
R. Boyer, G. Welsch, and E. W. Collins, editors, Materials Properties Handbook, Titanium
Alloys, ASM International, Materials Park, OH, 1994.
E. Kelly, Electrochemical behavior of titanium, Mod. Aspects Electrochem. 14, 319
(1982).
R. W. Schulz, Corrosion of titanium and titanium alloys, in ASM Handbook, Vol. 13B,
Corrosion: Materials, ASM International, Materials Park, OH, 2005, pp. 252–299.
PROBLEM
1. Using the polarization curve for titanium in sulfuric acid, show the effect of
alloying with palladium or platinum and explain the reduction of corrosion
rate in the alloyed material compared to pure titanium.
26
ZIRCONIUM
26.1 INTRODUCTION
Zirconium is an active metal in the Emf Series, normally exhibiting very stable
passivity. As illustrated in Fig. 26.1, zirconium is passive over a very wide range
of potential and pH [1].
The metal [m.p. = 1852 °C (3366°F); density = 6.45 g/cm3] reacts readily
at elevated temperatures with O2, N2, and H2. At temperatures below ∼860 °C,
α-zirconium, hexagonal close-packed (hcp) structure, is the stable form,
which transforms to body-centered cubic (bcc), β-zirconium, at higher
temperatures.
An unusual property is the high solid solubility of the metal for oxygen, with
the metal dissolving up to 29 at.% (6.7 wt.%) according to the oxygen–zirconium
phase diagram [2]. Similarly, α-zirconium absorbs nitrogen in solid solution up
to 25 at.% (4.8 wt.%). It reacts with air to form both zirconium oxides and
nitrides. The reaction is slow enough, however, to permit hot rolling at 600–750 °C
(1100–1400°F) [3].

435
436 ZIRCONIUM
–2 0 2 4 6 8 10 12 14 16
2 2
1.6 1.6
b
1.2 1.2
0.8 0.8
corrosion
0.4 0.4
passivation
0 a 0
corrosion
–0.4 –0.4
–0.8 –0.8
–1.2 –1.2
–1.6 –1.6
–2 –2
–2.4 immunity –2.4

–2 0 2 4 6 8 10 12 14 16
pH
Figure 26.1. Theoretical conditions of corrosion, immunity, and passivation of zirconium at

25 °C, assuming passivation by ZrO2·2H2O [1]. (M. Pourbaix, Atlas of Electrochemical Equilibria
in Aqueous Solutions, 2nd English edition, p. 227. Copyright NACE International 1974 and
CEBELCOR.)
26.2 ZIRCONIUM ALLOYS
Because of good corrosion resistance in both acids and bases, zirconium alloys
are widely used in chemical plants. Commercial zirconium, as used primarily for
corrosion resistance in the chemical industry [4], contains up to 4.5% hafnium,
which is difficult to separate because of the similar chemical properties of zirco-
nium and hafnium. The presence or absence of hafnium has no effect on the
corrosion resistance, which is controlled by a very stable oxide. At ambient tem-
perature, this passive oxide is 2–5 nm thick [4]. The pure metal low in hafnium
(0.02% max) has a low thermal neutron capture, making it useful for nuclear-
power applications.
The outstanding corrosion property of zirconium is its resistance to alkalies
at all concentrations up to the boiling point. It also resists fused sodium hydrox-
ide. In this respect, it is distinguished from tantalum and, to a lesser extent, tita-
nium, which are attacked by hot alkalies. Zirconium is resistant to hydrochloric
and nitric acids at all concentrations and to <70% H2SO4 up to boiling tempera-
tures. In HCl and similar media, the metal must be low in carbon (<0.06%) for
optimum resistance. In boiling 20% HCl, a transition or “breakaway” point is
observed in the corrosion rate (see below) after a specific time of exposure. The
BEHAVIOR IN HOT WATER AND STEAM 437
final rate, which is higher than the initial rate, is usually less than 0.11 mm/y
(0.0045 ipy) [5]. Zirconium is not resistant to oxidizing metal chlorides (e.g., FeCl3;
pitting occurs), nor is it resistant to HF or fluosilicic acid.
Critical pitting potentials of 0.38 V (S.H.E.) in 1 N NaCl and 0.45 V in 0.1 N
NaCl [6] indicate that the metal is vulnerable to pitting in seawater. It undergoes
intergranular S.C.C. in anhydrous methyl or ethyl alcohol containing HCl, but
not when a small amount of water is added [7]. This behavior, similar to that of
commercial titanium, suggests that stress may not be necessary and that the
failure is perhaps better described as intergranular corrosion.
Although zirconium alloys do have good resistance to S.C.C., they are sus-
ceptible in many environments. In general, weldments should be heat-treated to
reduce residual stresses. Unalloyed zirconium has been reported to be resistant
to S.C.C. because of its low yield strength, whereas the higher-strength alloys are
more susceptible. Cracking can be intergranular, transgranular, or mixed inter-
granular/transgranular [8]. In Zr–2.5% Nb, not only S.C.C., but also a delayed
hydride cracking process, can occur at highly stressed locations [8–11].
In the nuclear industry, zirconium alloys are used as nuclear fuel cladding
and structural fuel assembly components (see Section 8.5). The intense radiation
within the reactor core accelerates degradation by increasing the rates of corro-
sion and hydriding. Zircaloy-2 (Zr, 1.5% Sn, 0.1% Fe, 0.1% Cr, 0.05% Ni), an
alloy used in nuclear reactors, is subject to S.C.C. in chlorides at 25 °C at potentials
noble to the breakdown potential of the air-formed oxide film [0.34 V (S.H.E.)
in 5% NaCl] [12]. Stress-corrosion cracking may also occur in FeCl3 and CuCl2
solutions [13]. In slow strain rate tests, commercially pure zirconium, Zircaloy-2,
and Zircaloy-4 (Zr, 1.5% Sn, 0.2% Fe, 0.1% Cr) undergo S.C.C. in >20% HNO3
at 25 °C with the maximum cracking rate in 70–90% HNO3. Unlike the situation
for titanium, the presence of NO2 does not have a significantly damaging effect
[14]. Constant strain (U-bend, C-ring) tests of commercial zirconium and some
zirconium alloys in 70% HNO3 up to the boiling point showed high resistance to
SCC, but not necessarily immunity [15]. Both zirconium and Zircaloy-2 are
subject to SCC in iodine vapor (a major fission product of uranium) at 300–350 °C
[16, 17]. Cold work and irradiation hardening have been reported to increase
susceptibility.
To help improve the corrosion resistance of Zircaloy, several new zirconium
alloys have been developed, such as Zirlo (Zr–1.0% Nb–1.0% Sn–0.1% Fe).
Notwithstanding the progress so far, materials reliability does have a significant
effect on the economics of nuclear power plants, and there is considerable incen-
tive to develop a full understanding of the mechanisms of corrosion of zirconium
alloys in reactors and to develop alloys that are resistant to both irradiation and
corrosion in reactors [18].
26.3 BEHAVIOR IN HOT WATER AND STEAM
The good resistance of zirconium to deaerated hot water and steam is of special
importance in nuclear-power applications. The metal or its alloys can be exposed
438 ZIRCONIUM
in general for prolonged periods without pronounced attack at temperatures

below about 425 °C (800°F). The rate of attack is characteristically low at first;
but after a certain time of exposure, ranging from minutes to years depending
on temperature, the rate suddenly increases. This “transition” phenomenon is
reported to occur for pure or impure zirconium after a weight gain on the order
of 3.5–5.0 g/m2, and similar additional accelerated oxidation may occur at still
higher weight gains [19]. It occurs at lower temperatures if the zirconium is con-
taminated with nitrogen (>0.005%) or with carbon (>0.04%) [20]. The damaging
effect of nitrogen in this respect is offset by alloying additions of 1.5–2.5% tin in
combination with lesser amounts of iron, nickel, and chromium.
Marker experiments indicate that oxidation proceeds by diffusion of oxygen
ions toward the metal–oxide interface (anion defect lattice). It has been sug-
gested on this basis that trivalent nitrogen ions in the ZrO2 lattice increase anion-
defect concentration, thereby increasing the diffusion rate of oxygen ions. But
were this the mechanism, oxidation in oxygen would also be affected, which is
not the case. Adding to the complexity is the observation that alloyed tin appre-
ciably shortens corrosion life of zirconium in water; but tin in the presence of
small amounts of alloyed iron, nickel, or, to a lesser extent, chromium again
increases corrosion resistance, with the combination overcoming the detrimental
effect of alloyed nitrogen.
The mechanism accounting for the transition phenomenon is not well under-
stood. It has been explained on the basis of cracks forming in the oxide because
of stresses accumulating as the oxide thickens. However, an increased corrosion
rate does not occur when the metal oxidizes in oxygen except for much longer
times and much thicker oxide films. Hydrogen formed by the decomposition of
H2O during reaction appears to exert a dominant role, especially that portion
which dissolves in the metal, causing higher oxidation rates [19]. X-ray data for
the oxides that form in H2O show a monoclinic modification of ZrO2 either
before or after the breakaway time, but with some evidence that the initial oxide
is a tetragonal modification [20].
The oxidation behavior of Zircaloy-2 in water and steam is shown in
Fig. 26.2.
In brief, zirconium is resistant to the following:
1. Alkalies, all concentrations up to boiling point, including fused

caustic.
2. Hydrochloric acid, all concentration up to boiling point. Embrittlement of
metal and higher corrosion rates occur above boiling temperatures under
pressure.
3. Nitric acid, all concentrations up to boiling point, including red fuming
acid (S.C.C. may occur under slow strain rate conditions [14]).
4. Sulfuric acid, <70%, boiling.
5. Phosphoric acid, <55% H3PO4, boiling.
6. Boiling formic, acetic, lactic, or citric acids.
REFERENCES 439
Figure 26.2. Corrosion of Zircaloy-2 in high-temperature water and steam, showing transi-
tion points [19].
Zirconium is not resistant to the following:
1. Oxidizing metal chlorides (e.g., FeCl3 and CuCl2).

2. Hydrofluoric acid and fluosilicic acid.
3. Wet chlorine.
4. Oxygen, nitrogen, and hydrogen at elevated temperatures.
5. Aqua regia.
6. Trichloroacetic or oxalic acids, boiling.
7. Boiling CaCl2, >55% [21].
8. Carbon tetrachloride, 200 °C (explodes) [22].
REFERENCES

Brussels, 1974, p. 227.
2. M. Hansen, Constitution of Binary Alloys, McGraw-Hill, New York, 1958, p. 1079.
3. W. Hurford, in The Metallurgy of Zirconium, B. Lustman and F. Kerze, Jr., editors,
McGraw-Hill, New York, 1955, p. 263.
440 ZIRCONIUM
4. B. Cox, Zirconium alloy corrosion, in Uhlig’s Corrosion Handbook, 2nd edition, R. W.

5. W. Kuhn, Corrosion 15, 103t (1959).
6. J. Kolotyrkin, Corrosion 19, 261t (1963).
7. K. Mori, A. Takamura, and T. Shimose, Corrosion 22, 29 (1966).
8. Ref. 4, p. 908.
9. B. A. Cheadle, C. E. Coleman, and J. F. R. Ambler, Prevention of delayed hydroide crack-
ing in zirconium alloys, ASTM STP 939, 1987, pp. 224–240.
10. F. H. Huang and W. J. Mills, Met. Trans. A 22A, 2049 (1991).
11. J. W. Mills and F. H. Huang, Eng. Fracture Mech. 39, 39, 241 (1991).
12. B. Cox, Corrosion 29, 157 (1973).
13. B. Cox, Rev. Coatings Corros. 1, 366 (1974).
14. J. Beavers, J. Griess, and W. Boyd, Corrosion 37, 292 (1981).
15. Te-Lin Yau, Corrosion 39, 167 (1983).
16. B. Cox, Corrosion 28, 207 (1972); ibid. 33, 79 (1977); B. Cox and J. C. Wood, in Corro-
sion Problems in Energy Conversion and Generation, C. Tedmon, editor, Electrochemi-
cal Society, Princeton, NJ, 1974, p. 275.
17. R. Gangloff et al., Corrosion 35, 316 (1979).
18. J. Busby, Irradiation effects on corrosion of zirconium alloys, in ASM Handbook, Vol.
13C, Corrosion: Environments and Industries, ASM International, Materials Park, OH,
2006, pp. 406–408. See also C. Lemaignan, Corrosion of zirconium alloy components
in light water reactors, in ASM Handbook, Vol. 13C, Corrosion: Environments and
Industries, ASM International, Materials Park, OH 2006, pp. 415–420.
19. B. Cox, Corrosion 18, 33t (1962).
20. D. Thomas, in The Metallurgy of Zirconium, B. Lustman and F. Kerze, Jr., editors,
McGraw-Hill, New York, 1955, pp. 608–640.
21. P. Gegner and W. Wilson, Corrosion 15, 341t (1959).
22. W. Archer and M. Harter, Corrosion 34, 159 (1978).
GENERAL REFERENCES
B. Cox, Zirconium alloy corrosion, in Uhlig’s Corrosion Handbook, 2nd edition, R. W.

B. Cox, J. Nucl. Mater. 170, 1 (1990).
B. Cox, Oxidation of zirconium and its alloys, Advances in Corrosion Science and Technol-
ogy, Vol. 5, M. Fontana and R. Staehle, editors, Plenum Press, New York, 1976, p. 173.
IAEA-TECDOC-996 (1998) Waterside corrosion of zirconium alloys in nuclear power
plants, International Atomic Energy Agency, Vienna, 1998.
Te-Lin Yau and R. C. Sutherlin, Corrosion of zirconium and zirconium alloys, in ASM
Handbook, Vol. 13B, Corrosion: Materials, ASM International, Materials Park, OH,
2005, pp. 300–324.
27
TANTALUM
27.1 INTRODUCTION
Tantalum [m.p. = 3000 °C (5430°F); density = 16.6 g/cm3] exhibits the most stable
passivity among known metals, as expected from the theoretical potential–pH
domains of immunity and passivation shown in Figure 27.1 [1]. Tantalum retains
passivity in boiling acids (e.g., HCl, HNO3, or H2SO4) and in moist chlorine or
FeCl3 solutions above room temperature. Corrosion resistance of this order sug-
gests a Flade potential much more active than the hydrogen electrode potential,
and a low passive current that is insensitive to Cl−.
27.2 CORROSION BEHAVIOR
High corrosion resistance to acids makes tantalum useful for special applications
in the chemical industry (e.g., H2SO4 concentrators and HCl absorption systems).
Liners of tantalum sheet may average only 0.3 mm (0.013 in.) thick, permitting
varied applications of the metal despite high cost.
Tantalum is attacked by alkalies and by hydrofluoric acid. It is readily embrit-
tled by hydrogen at room temperature when the metal is cathodically polarized,

441
442 TANTALUM
–2 0 2 4 6 8 10 12 14 16
2 2
1.6 1.6
1.2 b 1.2
0.8 0.8
0.4 0.4
passivation
0 a 0
–0.4 –0.4
–0.8 –0.8
–1.2 –1.2
–1.6 immunity –1.6
–2 –2
–2 0 2 4 6 8 10 12 14 16
pH
Figure 27.1. Theoretical potential–pH domains of immunity and passivation for tantalum at
25 °C [1]. (M. Pourbaix, Atlas of Electrochemical Equilibria in Aqueous Solutions, 2nd English
edition, p. 254. Copyright NACE International 1974 and CEBELCOR.)
or when coupled in an electrolyte to a metal more active in the Galvanic Series.

The damage by cathodic hydrogen can be avoided by coupling tantalum to a very
small area of a low-overpotential metal, such as platinum [2]. Hydrogen ions then
discharge on the platinum instead of entering the tantalum lattice. The benefit of
coupled platinum extends to avoiding embrittlement caused by hydrogen gener-
ated through a corrosion reaction. For example, even though tantalum is not
embrittled by concentrated hydrochloric acid at boiling temperatures, it becomes
embrittled at 190 °C (375°F) under pressure. This damage does not occur if an
area ratio of platinum to tantalum is provided on the order of at least 1 : 10,000.
Platinum can be attached to tantalum by riveting, welding, or electrodeposition.
Metal embrittled by cathodic hydrogen or by that entering at elevated tempera-
tures can be restored to normal properties only by heating in vacuum.
Fischer [3] reported that tantalum, despite its pronounced passivity in aqueous
media, corrodes generally in anhydrous CH3OH–Br2 mixtures at room tempera-
ture and undergoes pitting corrosion in CH3OH, 10% Br2, 4% H2O. Palit and
Elayaperumal [4] stated that tantalum is subject to pitting in CH3OH + 0.4 vol.%
concentrated HCl at potentials slightly noble to the corrosion potential in this
solution.
In brief, tantalum is resistant to the following:
1. Hydrochloric acid, all concentrations up to boiling point.

2. Nitric acid, all concentrations up to and above boiling point.
GENER AL REFERENCE 443
3. Sulfuric acid, all concentrations (except fuming) <175 °C (<350°F). Fuming

acid attacks tantalum at room temperature.
4. Chromic acid, hot or cold.
5. Phosphoric acid. Resistant to all concentrations up to and, in some cases,
above boiling temperatures. For 85% H3PO4 at 225 °C, rate = 0.09 mm/y
(0.0035 ipy). Attack occurs at lower temperatures when the acid is con-
taminated with HF (>4 ppm).
6. Halogen gases [wet or dry Cl2 up to 150 °C (300°F); Br2 up to 175 °C
(350°F)].
7. Aqua regia.
8. Oxidizing metal chlorides, hot or cold (e.g., FeCl3 and CuCl2).
9. Organic acids: lactic, oxalic, and acetic.
Tantalum is not resistant to the following:
1. Alkalies. Embrittlement occurs, for example, with 5% NaOH, 100 °C.

2. Hydrofluoric acid and fluorides, trace amounts.
3. Fuming sulfuric acid.
4. Oxygen, nitrogen, or hydrogen at elevated temperatures. Oxidation in air
becomes appreciable above 250 °C (500°F). Cathodic hydrogen causes
embrittlement at room temperature.
5. Methanol solutions of Br2 or HCl.
REFERENCES

Brussels, 1974, p. 254.
2. C. Bishop and M. Stern, Corrosion 17, 379t (1961).
3. W. Fischer, Tech. Mitt. Krupp. 22, 125 (1964).
4. G. Palit and K. Elayaperumal, Corros. Sci. 18, 169 (1978).
GENERAL REFERENCE
Corrosion of tantalum and tantalum alloys, in ASM Handbook, Vol. 13B, Corrosion: Mate-
rials, ASM International, Materials Park, OH, 2005, pp. 337–353.
28
LEAD
28.1 INTRODUCTION
Pb2+ + 2e − → Pb φ = −0.126 V
Lead is a relatively active metal in the Emf Series, becoming passive in many
corrosive media that form insoluble lead compounds (e.g., H2SO4, HF, H3PO4,
and H2CrO4) by reason of thick diffusion-barrier coatings (Definition 2, Section
6.1). In these acids, corrosion resistance is good provided relative velocity of
metal and acid is below the value that causes erosion of protective films. Lead is
used, therefore, in the chemical industry as lining and piping. The metal is,
however, corroded by dilute nitric acid and by several dilute aerated organic acids
(e.g., acetic and formic acids).
The theoretical potential–pH domains for corrosion, immunity, and passiv-
ation are shown in Figure 28.1 [1]. As shown in the diagram, in acid or neutral
solution, lead can be cathodically protected by controlling the potential to less
than −0.3 V. In alkaline solution, potential control for cathodic protection is below
−0.4 to −0.8 V, depending on the pH [1].

445
446 LEAD
–2 0 2 4 6 8 10 12 14 16
2 2
E(V)
1.6 passivation 1.6
1.2 b 1.2
0.8 0.8
0.4 0.4
corrosion
0 a 0
–0.4 –0.4
–0.8 –0.8
immunity
–1.2 –1.2
–1.6 –1.6
–2 –2
corrosion
–2.4 –2.4
–2 0 2 4 6 8 10 12 14 pH
lead at 25 °C [1]. (M. Pourbaix, Atlas of Electrochemical Equilibria in Aqueous Solutions, 2nd
English edition, p. 490. Copyright NACE International 1974 and CEBELCOR.)
28.2 CORROSION BEHAVIOR OF LEAD AND LEAD ALLOYS
Being amphoteric, lead is corroded by alkalies at moderate or high rates, depend-

ing on aeration, temperature, and concentration. Nevertheless, lead resists corro-
sion in many environments because the products of corrosion are insoluble and
form self-healing protective films. Because of these protective films, the corrosion
rate of lead is usually under anodic control [2].
It is attacked, for example, by calcium hydroxide solutions at room tempera-
ture, including waters that have been in contact with fresh Portland cement.
Organic acids harmful to lead can be leached from wood structures, particularly
damp timber including western cedar, oak, and Douglas fir. This cause of corro-
sion can be prevented by fully drying the wood, treating it to prevent contact
with moist air, or inserting a moisture barrier between wood and lead [3].
An alloy of 2% Ag–Pb is used as a corrosion-resistant anode in impressed
current systems for cathodic protection of structures in seawater (see Section
13.6) [4]. Alloying with 6–12% Sb increases strength [only at temperatures <120 °C
(<250°F)] of the otherwise weak metal, but corrosion resistance of the alloy in
some media is below that of pure lead.
Lead is resistant to seawater. It is also durable for use in contact with fresh
waters; however, the toxic properties of trace amounts of lead salts make it man-
CORROSION BEHAVIOR OF LEAD AND LEAD ALLOYS 447
datory to exclude its use, and the use of its alloys, for soft potable waters, carbon-
ated beverages, and all food products. The U.S. Environmental Protection Agency
(EPA) Lead and Copper Rule, implemented in 1991, limits lead in potable water
to a maximum of 15 ppb [5]. The rate of corrosion in aerated distilled water is
high (approximately 9 gmd) and the rate increases with concentration of dis-
solved oxygen [6]. In the absence of dissolved oxygen, the corrosion rate in waters
or dilute acids is either negligible or very low.
Lead is resistant to atmospheric exposures, particularly to industrial atmo-
spheres in which a protective film of lead sulfate forms. Buried underground, the
corrosion rate may exceed that of steel in some soils (e.g., those containing
organic acids), but in soils high in sulfates the rate is low. Soluble silicates, which
are components of many soils and natural waters, also act as effective corrosion
inhibitors.
Lead is used in solder alloys (typically with 5%tin, and a small amount of
silver to increase strength) for joints of automobile radiators [7].
In applications where thermal cycling occurs, the high coefficient of expan-
sion (30 × 10−6/°C) of lead may cause intergranular cracking due to fatigue or
corrosion fatigue.
28.2.1 Lead–Acid Battery

Lead–acid batteries are a principal use of lead. Following are the reactions that
take place during discharge of a lead–acid battery [8]:
At the anode: Pb → Pb2+ + 2e − (28.1)
At the cathode: PbO2 + 4 H + + 2e − → Pb2+ + 2 H 2O (28.2)
The net reaction: Pb + PbO2 + 4H + → 2Pb2+ + 2 H 2O (28.3)
Corrosion of lead in Eq. (28.1) is part of the overall electrochemical reaction by

which electrical energy is generated using the lead–acid battery. In addition to
this positive and beneficial aspect of corrosion in energy generation, corrosion
can also lead to shorter battery lifetime and reduced capacity to produce energy.
For example, corrosion during battery storage reduces the quantity of lead avail-
able for energy production and may also produce corrosion products that inhibit
the corrosion that takes place by Eq. (28.1). Passivation of the lead anode increases
the anodic overvoltage, decreases the current, and causes a deterioration of
battery performance. The lead–acid battery uses lead grids at both the anode and
the cathode. Corrosion of lead at the cathode has been reported to cause loss of
capacity of batteries [9]. For corrosion by Eq. (28.1), which results in energy
production, the overvoltage should be as low as possible. For the destructive
forms of corrosion, which lead to reduced battery lifetime and capacity, the over-
voltage should be as high as possible [10].
448 LEAD
Various alloys of lead are used as support grids for positive and negative
plates of lead–acid batteries. Alloying elements are added to improve mechani-
cal properties, but anodic corrosion of these alloys can limit battery lifetime
[11, 12]. Lead–antimony alloys, containing typically about 5% antimony, have
been used for many years [13]. These alloys develop an adherent protective
corrosion product layer; however, the deposition of antimony on the negative
plate lowers the hydrogen overpotential [13, 14]. Furthermore, on overcharge,
toxic stibine (SbH3) is produced. For these reasons, alloys of lead with calcium,
tin, and aluminum are also being used [13, 14]. Other possible alloying elements
that have been studied include magnesium, titanium, and bismuth [14, 15].
Lead–calcium–tin alloys used as grid material for maintenance-free batteries
have been reported to be susceptible to intergranular corrosion at large grain
sizes [16].
28.3 SUMMARY
In summary, lead is resistant to the following:
1. Many strong acids.

a. H2SO4, <96%, room temperature; the rate for <80% H2SO4, boiling, is
<2 mm/y (<0.08 ipy); for 20% H2SO4, boiling, the rate is 0.08 mm/y
(0.003 ipy) [17].
b. Commercial H3PO4 (hot or cold).
c. H2CrO4 (as used in chromium plating).
d. HF <60–65% (room temperature).
e. H2SO3.
2. Atmospheric exposures, particularly industrial.
3. Seawater (0.01 mm/y, 0.0005 ipy).
4. Chlorine, wet or dry, <100 °C (but only dry Br2 and at lower temperatures),
SO2, SO3, H2S.
Lead is not resistant to the following:
1. HNO3, <70%.
2. HCl.
3. Concentrated H2SO4 (>96%, room temperature).
4. Alkalies. For some chemical applications, the rate in caustic alkalies is
considered tolerable.
5. HF, gaseous.
6. Many aerated organic acids.
REFERENCES

Brussels, 1974, p. 490.
2. F. E. Goodwin, Lead and lead alloys, in Uhlig’s Corrosion Handbook, 2nd edition, R.
W. Revie, editor, Wiley, New York, 2000, p. 768.
3. Ref. 2, p. 775.
4. R. H. Heidersbach, Cathodic protection, in ASM Handbook, Vol. 13A, Corrosion: Fun-
p. 860.
5. Environmental Protection Agency website: http://www.epa.gov/safewater/lcmr/
6. Ref. 2, p. 770.
7. S. J. Alhassan, Corrosion of lead and lead alloys, in ASM Handbook, Vol. 13B, Corro-
sion: Materials, ASM International, Materials Park, OH, 2003, p. 203.
8. M. Pourbaix, Lectures on Electrochemical Corrosion, third English edition, J. A. S.
Green, translator, R. W. Staehle, editor, NACE International, Houston, TX, 1995,
p. 91.
9. D. Pavlov, J. Power Sources 46, 171 (1993); ibid., 48, 179 (1994); ibid., 53, 9 (1995).
10. C. F. Windisch, Anodes for batteries, in ASM Handbook, Vol. 13A, Corrosion: Funda-
pp. 170–177.
11. P. Ruetschi, in Lead–Acid Batteries: A Reference and Data Book, Elsevier, Lausanne,
Switzerland, 1977, pp. 19–21.
12. C. Dacres, S. Reamer, R. Sutula, and I. Angres, J. Electrochem. Soc. 128, 2060 (1981).
13. N. Hampson, S. Kelly, and K. Peters, J. Appl. Electrochem. 19, 91 (1980).
14. J. Bialacki, N. Hampson, and K. Peters, J. Electrochem. Soc. 130, 1797 (1983).
15. N. Hampson, S. Kelly, and K. Peters, J. Electrochem. Soc. 127, 1456 (1980).
16. M. V. Rose and J. A. Young, in Proceedings of the Fifth International Conference on
Lead, Metal Bulletin Limited, London, 1976, p. 37.
17. Ref. 2, pp. 771–775.
GENERAL REFERENCES
S. J. Alhassan, Corrosion of lead and lead alloys, in ASM Handbook, Vol. 13B, Corrosion:
F. E. Goodwin, Lead and lead alloys, in Uhlig’s Corrosion Handbook, 2nd edition, R. W.
D. Pavlov, Essentials of Lead–Acid Batteries, Society for Advancement of Electrochemical
Science and Technology, Karaikudi, India, 2006.
C. F. Windisch, Anodes for batteries, in ASM Handbook, Vol. 13A, Corrosion: Fundamen-
tals, Testing, and Protection, ASM International, Materials Park, OH, 2003, pp.
170–177.
29
APPENDIX
29.1 ACTIVITY AND ACTIVITY COEFFICIENTS OF

STRONG ELECTROLYTES
Let μ be the partial molal free energy, μ° the partial molal free energy in the
standard state (a = 1), a the activity, M the molality, and γ the activity
coefficient.
By definition,
μ = μ° + RT ln a
a = γM
where γ → 1 as M → 0.
For a binary electrolyte of molality M, assuming total dissociation,
μ = μ° + RT ln a− + RT ln a+
= μ° + RT ln γ − M− + RT ln γ + M+
= μ° + 2 RT ln γ ± M

451
452 APPENDIX
where M− = M+ = M, and γ± is the mean ion activity coefficient (it is impossible

to measure the activities of individual ions). For an electrolyte such as lanthanum
sulfate of molality M, we have
La 2 (SO4 )3 → 2La 3+ + 3SO24 −
μ = μ° + 2 RT ln γ ± MLa 3+ + 3RT ln γ ± MSO2−

4
Since MLa 3+ = 2 M and MSO2− = 3M ,

4
μ = μ° + RT ln γ 5± (2 M )2 (3M )3
= μ° + 5RT ln γ ± M (2 2 × 33)1/ 5
For the general case in which one mole of electrolyte dissociates into ν1 moles
of cation and ν2 moles of anion, the mean activity is given by
a± = γ ± M (v1v1 v2v2 )1 /( v1+ v2 )
(See also: C. W. Davies, Electrochemistry, George Newnes, Ltd., London, 1967;

J. O’M. Bockris and A. K. N. Reddy, Modern Electrochemistry, 2nd edition, Vol.
1: Ionics, Plenum, New York, 1998, pp. 251–257.) Activity coefficients are listed
in Table 29.1.
Example. Calculate the emf of the following cell:
Zn; ZnCl 2 (0.01M ); Pt(Cl 2 , 0.5 atm)
γ ± for 0.01M ZnCl 2 = 0.71 (Table 29.1)
Zn 2 + + 2e − → Zn φ° = −0.763 V (29.1)
Cl 2 + 2e − → 2Cl − φ° = 1.360 V (29.2)
Tentative reaction: (29.2)– (29.1)
Zn + Cl 2 → Zn 2 + + 2Cl − (29.3)
The corresponding Nernst equation is
0.0592 (Zn 2+ )(Cl − )2

E = 0.763 + 1.360 − log
2 pCl 2
0.0592 (0.01)(0.71)[(0.02)(0.71)]2
= 2.123 − log
2 0.5
= 2.29 V
TABLE 29.1. Activity Coefficients of Strong Electrolytes (M = molality)
ACTIVIT Y AND ACTIVIT Y COEFFICIENTS OF STRONG ELECTROLY TES
453
454
TABLE 29.1. Continued

APPENDIX
ACTIVIT Y AND ACTIVIT Y COEFFICIENTS OF STRONG ELECTROLY TES 455
456 APPENDIX
[Reaction (29.3) is spontaneous (ΔG is negative); zinc is anode (−), and platinum
is cathode (+)].
29.2 DERIVATION OF STERN–GEARY EQUATION FOR

CALCULATING CORROSION RATES FROM POLARIZATION
DATA OBTAINED AT LOW CURRENT DENSITIES
Assume that the corrosion current, Icorr, occurs at a value within the Tafel region
for both anodic and cathodic reactions. Also assume that concentration polariza-
tion and IR drop are negligible. Current relations are shown in Fig. 29.1 for the
corroding metal polarized as anode by means of an external current to a potential
φ. Increasing anodic current, Ia, is accompanied by decreasing cathodic current,
Ic, because of the relation,
Iappl = I a − I c (29.4)
Similarly, for cathodic polarization, for which Iappl changes sign, we have
− I appl = I c − I a (29.5)
For anodic polarization, we obtain
Figure 29.1. Polarization diagram for corroding metal polarized anodically from φcorr to φ.
DERIVATION OF STERN-GEARY EQUATION FOR CALCUL ATING CORROSION R ATES 457
Ia I
φ − φcorr = Δφ = βa log − βa log corr
ioa Aa ioa Aa
(29.6)
Ia
= βa log
I corr
where Aa is the fraction of area that is anode, and i0a is the exchange current
density for the anodic reaction. Note that i0a in the Tafel equation refers to
current per unit local area (not total area); hence, Icorr/Aa is the current density
to which i0a applies. Likewise, if the metal is polarized an equal amount in the
cathodic direction, we have
Ic
Δφ = −βc log (29.7)
I corr
or
I c = I corr 10 − Δφ/βc and I a = I corr 10 Δφ/βa
then
Iappl = I corr (10 Δφ/βa − 10 − Δφ/βc ) (29.8)
Expressed as a series, we have
(2.3 x)2
10 x = 1 + 2.3 x + +
2!
If Δφ/βc and Δφ/βa are small, higher terms can be neglected and (29.8) can be
approximated by
Iappl = 2.3I corr Δφ ⎛ + ⎞

1 1
(29.9)
⎝ βc βa ⎠
or
I appl ⎛ βaβc ⎞ 1 ⎛ βaβc ⎞

I corr = ⎜⎝ ⎟⎠ = ⎜ ⎟ (29.10)
2.3Δφ βa + βc 2.3R ⎝ βa + βc ⎠
where R is the polarization resistance, determined experimentally by applying

both anodic and cathodic currents to the electrode and measuring the polariza-
tion. The value of R used in Eq. (29.10) is the slope of the φ versus I graph at
the corrosion potential.
458 APPENDIX
Figure 29.2. Polarization diagram for metal corroding under control by oxygen
depolarization.
Equation (29.10) is the Stern–Geary equation. Should the cathodic reaction

be controlled by concentration polarization, as occurs in corrosion reactions
controlled by oxygen depolarization, the corrosion current equals the limiting
diffusion current (Fig. 29.2). This situation is equivalent to a large or infinite
value of βc in (29.10). Under these conditions, (29.10) becomes
βa Iappl β
I corr = = a (29.11)
2.3Δφ 2.3R
If a noncorroding metal (minimum local action) that polarizes only slightly

(high value of i0a) is polarized anodically at moderate current densities, then i0a
can be substituted for Icorr in Fig. 29.1, and
I appl βc βa
Δφ = (29.12)
2.3ioa βa + βc
indicating, as observed, that anodic polarization of many metals at low current

densities is a linear function of applied current.
29.2.1 The General Equation

If φcorr falls outside the Tafel region, for example, when it approaches either the
reversible anode or cathode potential, “back-reactions” become appreciable and
(29.10) is subject to error. Mansfeld and Oldham [1] considered this case and
DERIVATION OF STERN-GEARY EQUATION FOR CALCUL ATING CORROSION R ATES 459
formulated the required modifications. The derivation of the more exact form of
(29.10) starts with modifying (29.4). Because Iappl changes sign at potentials above
compared to below φcorr, choosing Iappl and Ia with the same sign—that is, anodic
polarization—results in
I appl = I a − I ar − ( I c − I cr ) (29.13)
where Iar and Icr are the back-reactions for the anodic and cathodic reactions,
respectively.
Introducing the Tafel equation expressed in natural logarithms, η = b ln(I/I0)
and letting ba = βa/2.3, bc = βc/2.3, bar = βar/2.3, and bcr = βcr/2.3, we have
I appl = Ioa exp ( φ − φa

ba )− I oa exp − (
φ − φa
bar )
− I oc exp −
φ − φc
bc (
+ I oc exp )
φ − φc
bcr ( )
(29.14)
According to electrode kinetics, we obtain
1 1 nF 1 1 nF
+ = a and + = c
ba bar RT bc bcr RT
where na and nc are constants related to the transfer coefficient. Using these rela-
tions to eliminate bar and bcr, it follows that
Iappl = Ioa exp (φ − φa ⎡

ba ⎣⎢ )
1 − exp a (
n F (φa − φ) ⎤
RT ⎦⎥ ) (29.15)
− I oc exp c (
φ −φ ⎡
bc ⎢
⎣ )
1 − exp c
RT (
n F (φ − φ c ) ⎤
⎦⎥ )
Differentiating (29.15) with respect to φ, we get
∂I appl I oa
∂φ
=
ba
exp
φ − φa ⎡
ba ⎣ ⎢( ) (
bnF
1 + a a − 1 exp a
RT
n F (φa − φ) ⎤
RT ⎥⎦ ) ( ) (29.16)
I
+ oc exp c
bc
φ −φ ⎡
bc ⎣⎢ ( ) (
bnF n F (φ − φ c ) ⎤
1 + c c − 1 exp c
RT RT ) (
⎦⎥ )
At the corrosion potential, Iappl = 0 and Ia = Ic = Icorr.
Letting Δφa = φcorr − φa and Δφc = φc − φcorr, (29.15) becomes
I corr = Ioa exp ( )

Δφa ⎡
ba ⎣⎢
1 − exp ( RT )
− na F Δφa ⎤
⎦⎥
(29.17)
= I oc exp ( )
Δφc
bc ⎣⎢ ( RT )⎦⎥
⎡1 − exp − n F Δφ ⎤
c c
(29.18)
460 APPENDIX
and (29.16) becomes
1 ⎛ ∂I appl ⎞
=⎜ ⎟
I
( ) (
= oa exp
R ⎝ ∂φ ⎠ φ = φcorr ba
Δφa ⎡
ba ⎣⎢
bnF
) (
1 + a a − 1 exp
RT
− na F Δφa ⎤
RT ⎦⎥ )
(29.19)
I
+ oc exp
bc ( ) (
Δφc
bc ⎣⎢) ( c
RT
c
RT ) ⎦⎥
⎡1 + b n F − 1 exp − n F Δφ ⎤
c c
Substituting (29.17) into the first part of (29.19) and (29.18) into the second part
of (29.19) gives
( ) ( )
−1 −1
1 ⎧1 1 nF
= I corr ⎨ + + a ⎡exp na F Δφa − 1⎤ + nc F ⎡exp nc F Δφc − 1⎤ ⎫ (29.20)
R ⎩ ba bc RT ⎢⎣ RT ⎥⎦ RT ⎢⎣ RT ⎥⎦ ⎬⎭
Equation (29.20) was developed by Mansfeld and Oldham [1] and is equivalent
to the one derived originally by Wagner and Traud [2]. If the correction terms
involving Δφa and Δφc can be neglected, (29.20) becomes the Stern–Geary equa-
tion. On the other hand, if either Δφa or Δφc approaches zero, the corresponding
correction term approaches infinity.
Small values of nFΔφ/RT allow the exponential terms to be expanded, sim-
plifying (29.20) to
= I corr ⎛⎜ + +
1 1 1 1 1 ⎞
+
⎝ ba bc Δφa Δφc ⎟⎠
(29.21)
R
If Δφc = 0.005 V, T = 298 °K, and nc is assumed to be 0.5, then F/RT = 39 V−1 and
ncFΔφc/RT = 0.1. The corresponding correction term from (29.20) is 190 V−1,
whereas the approximated correction term in (29.21) is 1/Δφc = 200 V−1. These
correction terms are large compared to 1/ba + 1/bc = 46 V−1 (assuming βa = βc =
0.1 V). Should Δφc = 0.1 V, the corresponding correction term from (29.20) is
3.2 V−1. If at the same time, Δφa = 0.5 V and na = 0.5, the correction term as given
by (29.20) equals 0.001 V−1, which is negligible.
Additional approximations [1] that could be used if the corrosion potential
is close to one of the reversible potentials are as follows. If naΔφa < 2RT/F (i.e.,
the corrosion potential is close to the reversible potential of the metal),
= I corr ⎛⎜ + + − a ⎞⎟
1 1 1 1 nF
(29.22)
R ⎝ ba bc Δφa 2 RT ⎠
If ncΔφc < 2RT/F (i.e., the corrosion potential is close to the reversible potential
of the reduction reaction), we obtain
= I corr ⎛⎜ + + − c ⎞⎟
1 1 1 1 nF
(29.23)
R ⎝ ba bc Δφc 2 RT ⎠
DERIVATION OF EQUATION EXPRESSING THE SATUR ATION INDEX 461
Figure 29.3. Relative errors in corrosion currents calculated by use of (29.10), (29.21), (29.22),
and (29.23), instead of the exact equation (29.20) [1] (with permission from Pergamon
Press).
The errors that result from each of these approximations to (29.20) are presented
in Fig. 29.3 [1], where na = 2, nc = 1, ba = RT/F, bc = 2 RT/F, and φc − φa = Δφa +
Δφc = 10 RT/F were assumed.
29.3 DERIVATION OF EQUATION EXPRESSING THE SATURATION

INDEX OF A NATURAL WATER
In accord with the discussion of saturation index in Section 7.2.6.1, we have
K s′ = (Ca 2 + )(CO23 − ) (29.24)
(H + )(CO32 − )
K 2′ = (29.25)
(HCO3− )
Assume that salts of weak acids other than carbonic acid are absent.
Then when a water is titrated, equivalents of added acid equal equivalents of
carbonate and bicarbonate, plus OH− or minus H+, depending on pH of the
water:
(alk) + (H + ) → 2(CO23 − ) + (HCO−3 ) + (OH − ) (29.26)

462 APPENDIX
where (alk) = alkalinity, or titratable equivalents of base per liter (by

titrating with acid) obtained by using methyl orange as indicator. Concentrations
of (H+) and (OH−) are small between pH values 4.5 and 10.3 and may be
neglected.
From Eq. (29.25), we obtain
K 2′ (HCO−3 )
(CO23 − ) = (29.27)
(H + )
From Eq. (29.26),
(alk) − (HCO−3 )
(CO23 − ) = (29.28)
2
Therefore,
(alk)
(HCO−3 ) = (29.29)
1 + 2 K 2′ /(H + )
Equation (29.29) was derived by Langelier [3] on the assumption that

K s′ and K 2′ are based on concentrations (moles/liter) rather than on activities.
For example, referring to (29.24), if Ks is the true activity product, then
K s = K s′γ 2± , where γ± refers to the mean ion activity coefficient for CaCO3. The
activity coefficient was approximated by Langelier using the Debye–Hückel
theory, −log γ = 0.5 z2 μ1/2, where μ is the ionic strength and z is the valence. Hence,
concentrations of CO2− 3 and HCO−3 obtained by titration can be equated to
corresponding concentrations of these species in K s′ and K 2′ . Accordingly, K s′
and K 2′ vary not only with temperature, but also with total dissolved
solids because of the effect of ionic strength of a solution on activities of
specific ions.
K 2′ (alk)
(CO23 − ) = (29.30)
(H + ) 1 + 2 K 2′ /(H + )
and substituting (29.30) into (29.24), we get
K 2′ (alk)
(Ca 2 + ) = K s′ (29.31)
(H + ) 1 + 2 K 2′ /(H + )
Taking logarithms of both sides and using the notation log 1/α = pα, we
obtain
TABLE 29.2. Values of log 1 + ( 2K2′

(H+ )s ) as a Function of pH
s
pHs: 10.3 10.0 9.7 9.4 9.1
( )
2 K 2′ 0.47 0.29 0.17 0.09 0.05
log 1 + :
(H + )s
2 K 2′ ⎞
pH s = pK 2′ − pK s′ + p(Ca 2 + ) + p(alk) + log ⎛⎜ 1 + ⎟ (29.32)
⎝ (H + )s ⎠
where pHs is the pH of a given water at which solid CaCO3 is in equilibrium with
its saturated solution.
The last term is ordinarily small and can be omitted when pHs < 9.5. Based
on the value K 2′ = 4.8 × 10 −11 , typical values as a function of pHs in the alkaline
range at 25°C are given in Table 29.2.
Values of ( pK 2′ − pK s′ ) decrease with increasing temperature as follows: 0°C,
2.48; 20°C, 2.04; 25°C, 1.96; 50°C, 1.54. In the presence of other salts (e.g., NaCl,
Na2SO4, or MgSO4), the increasing ionic strength of the solution depresses the
activity of other ions in solution. This effect increases values of ( pK 2′ − pK s′ ). For
example, at 25°C, at a total dissolved-solids content of 100 ppm, the value is 2.13,
and for 500 ppm it is 2.19.
A nomogram for obtaining pHs of a water at various temperatures and
dissolved-solids content was constructed by C. Hoover [4]. A chart for the same
purpose as prepared by Powell, Bacon, and Lill [5] is reproduced in Fig. 29.4.
To use the chart, we must know the alkalinity of a water and calcium ion con-
centration calculated as ppm CaCO3, total dissolved solids in ppm, and the
temperature.
The saturation index is then the algebraic difference between the measured
pH of a water and the computed pHs:
Saturation index = pH measured − pH s (29.33)
To calculate the saturation index at above-room temperature, the actual pH of

water at the higher temperature should be used. This can be estimated from the
room temperature value by using Fig. 29.5 [5], which gives values for two waters
of differing alkalinity.
464 APPENDIX
Figure 29.4. Chart for calculating saturation index (Powell, Bacon, and Lill [5]). (“Ca” and
“alkalinity” are expressed as ppm CaCO3, and temperature is expressed in °F.)
Figure 29.5. Values of pH of water at elevated temperatures (Powell, Bacon, and Lill [5]).
(a) For water at 25 ppm alkalinity (methyl orange end point). (b) For water of 100 ppm alkalin-
ity (methyl orange end point).
466 APPENDIX
Figure 29.5. Continued

DERIVATION OF POTENTIAL CHANGE ALONG A CPP 467
29.4 DERIVATION OF POTENTIAL CHANGE ALONG A

CATHODICALLY PROTECTED PIPELINE
Assume that current enters a pipe from the soil side through a porous insulating
coating, returning to the anode by way of the pipe (Fig. 29.6). Then the change
of current, Ix, in the pipe per unit length at x is equal to the total current entering
the pipe at x, or
dI x
= −2πrix (29.34)
dx
where r is the radius of the pipe.

By Ohm’s law, the potential change along the pipe is given by
dEx
= − RL I x (29.35)
dx
where RL is the resistance of metallic pipe per unit length. Combining (29.34)
and (29.35), we obtain
d 2 Ex
= RL (2 πrix ) (29.36)
dx 2
At small values of ix, polarization of the pipe surface is a linear function of the
true current density ix′ at the base of pores in the coating, or
Ex = k1ix′ (29.37)
Assuming that the resistance z per unit area of coating is inversely proportional
to the total cross-sectional area of pores per unit area, true current density
increases with z, or
Figure 29.6. Sketch of buried pipe cathodically protected by anodes distance a apart. ix is
the current density at pipe surface at distance x from point of bonding; Ix is the total current
in pipe at distance x; E is the difference between measured and corrosion potentials of pipe;
r is the radius of pipe; RL is the resistance of metallic pipe per unit length; and z is the resis-
tance of pipe coating per unit area.
468 APPENDIX
ix′ = k2 zix (29.38)
Combining (29.37) and (29.38), we get
Ex = kzix (29.39)
where k = k1k2.
Substituting (29.39) in (29.36), we obtain
d 2 Ex
dx 2
R 2 πr
= L
kz (Ex ) (29.40)
For an infinite pipeline, this differential equation has the solution
⎡ 2 πrRL
( )
1/ 2
⎤
Ex = EA exp ⎢ − x⎥ (29.41)
⎣ kz ⎦
for the boundary conditions Ex = 0 at x = ∞, and Ex = EA at x = 0.

On the other hand, if the length of pipeline to be protected is a/2, or half
the distance to the next point of bonding (see Fig. 29.6), and the potential Ex at
a/2 = EB, it follows that current in the pipeline at a/2 = 0, or (dEx/dx)x=a/2 = 0.
Introducing this boundary condition, we obtain
⎡ 2 πrRL
( ) ( x − a2 )⎤⎥⎦
1/ 2
Ex = EB cosh ⎢ (29.42)
⎣ kz
and
⎡ 2 πrRL
( )
1/ 2
a⎤
EA = EB cosh ⎢ − (29.43)
⎣ kz 2 ⎥⎦
The current in an infinite pipeline at any point x is given by substituting the

derivative of (29.41) into (29.35), or
( 2πkzrR ) ⎡ 2 πrRL
( )
1/ 2 1/ 2
EA ⎤
Ix = L
exp ⎢ − x⎥ (29.44)
RL ⎣ kz ⎦
The total current at x = 0 (sometimes called drainage current) multiplied by 2,

to account for current flowing from either side of the pipeline to the point of
bonding, equals
2 EA 2 πrRL
( )
1/ 2
IA = (29.45)
RL kz
DERIVATION OF THE EQUATION FOR POTENTIAL DROP ALONG THE SSC 469
Similarly, for a finite pipe, we have
( )( 2 πrRL
) (
⎡ a 2 πrRL
)
1/ 2 1/ 2
2 EB ⎤
IA = sinh ⎢ ⎥ (29.46)
RL kz ⎣2 kz ⎦
29.5 DERIVATION OF THE EQUATION FOR POTENTIAL DROP

ALONG THE SOIL SURFACE CREATED BY CURRENT ENTERING
OR LEAVING A BURIED PIPE
For a deeply buried pipe,
j
i= (29.47)
2πR
But for a pipe buried h cm below the soil surface, less current flows in the h
direction toward the soil surface than in other directions. The computation for
current flow in this situation is approximated by assuming an image pipe located
h cm above the soil surface that supplies an equal current j (Fig. 29.7). Then the
component of current density along the soil surface equals
2j y
iy = (29.48)
2πR R
Figure 29.7. Sketch of buried pipe at which current enters or leaves, causing potential drop
along soil surface.
470 APPENDIX
The same result can be obtained by assuming half-cylindrical current distribution

in the soil multiplied by the factor y/R to account for zero current flowing to the
pipe in the h direction (y = 0) and an increasing current density iy as distance y
increases.
By Ohm’s law, the potential gradient along the soil surface is
dφ j yρ
= (29.49)
dy πR R
Since R2 = h2 + y2, we have
y ρj y ρj y ρj h 2 + y2
Δφ = ∫0 ydy = ∫ dy = ln (29.50)
πR 2 0
π h 2 + y2 2π h2
If we take y = 10 times distance h, or y = 10h,
ρj
Δφ = 2.3 log 101 = 0.734ρj (29.51)
2π
where Δφ is in volts, ρ in Ω-cm, and j in A/cm. [See also, R. Howell, Corrosion

8, 300 (1952).]
29.6 DERIVATION OF THE EQUATION FOR DETERMINING

RESISTIVITY OF SOIL BY FOUR-ELECTRODE METHOD
Two metal electrodes, A and B, are at a distance 3a apart. Two reference elec-
trodes, C and D, are located distance a apart and also a from A and B, respec-
tively (see Fig. 29.8).
Figure 29.8. Sketch of four-electrode arrangement for determining soil resistivity.

DERIVATION OF THE EQUATION EXPRESSING WEIGHT LOSS 471
Assuming hemispherical symmetry at distance r from A or B, current density in

the soil = I/2πr2. By Ohm’s law,
dφ I
= ρ (29.52)
dr 2 πr 2
Iρ − Iρ 1
( )
r2
1
Δφ = ∫ 2 dr = 2π r − r (29.53)
r1 2 πr 2 1
Because current leaves A, the potential difference Δφ1 between C and

D is
Δφ1 = (
− Iρ 1 1
− =
2 π 2a a
Iρ
4 πa ) (29.54)
Similarly, the potential difference Δφ2 between C and D because of current enter-
ing electrode B is Iρ/4πa. Hence,
Iρ Δφ
Δφtotal = Δφ1 + Δφ 2 = or ρ = 2 πa (29.55)
2 πa I
[See also S. Ewing and J. Hutchinson, Corrosion 9, 221 (1953).]
29.7 DERIVATION OF THE EQUATION EXPRESSING WEIGHT LOSS

BY FRETTING CORROSION
Assume n asperities or contact points per unit area of metal (or oxide) surface
which, for mathematical convenience, are circular in shape. The average diame-
ter of asperities is c and the average distance apart is s (Fig. 8.21, Section 8.7.1).
In the fretting process, the asperities move over a plane surface of metal at linear
velocity υ, with each asperity plowing out a path of clean metal of width averag-
ing c and of length depending on distance of travel. Behind each asperity on the
track of clean metal, gas from the atmosphere adsorbs rapidly, followed in time
by formation of a thin oxide film. The next asperity, moving in the same path as
the first, scrapes the oxide film off and leaves, in turn, a track of clean metal
behind. The average time during which oxidation occurs is t. Then
s
t= (29.56)
υ
The corresponding amount of oxide W removed by one asperity plowing out a

path l long and c wide depends on the amount of oxide formed in time t. For
thin-film oxidation, the logarithmic equation is obeyed (see Section 11.4.1):
472 APPENDIX
W = clk ln ( τt + 1) (29.57)
where τ and k are constants.

Preliminary to oxidation, we can also consider the situation of oxygen adsorb-
ing rapidly as physically adsorbed gas, followed by conversion at a slower rate
to chemisorbed oxygen atoms. The chemisorbed oxygen, in turn, reacts with
underlying metal to form metal oxide, a reaction that is activated mechanically
by asperities moving over the metal surface. Chemisorption limits the amount of
oxide that is formed in such a process, the rate of chemisorption following an
equation identical in form to that of (29.57) [6]. Hence, whichever process applies,
the form of the final equation is essentially the same.*
W = clk ln ( υτs ) + 1 (29.58)
Assuming that relative motion of the two surfaces is sinusoidal, 2l is the total
length of travel in any one cycle and x, the linear displacement from the midpoint
of travel at time t, is given by
l
x= cosθ (29.59)
2
and
dx l dθ
= υ = − sin θ (29.60)
dt 2 dt
If f represents constant linear frequency, this is related to constant angular veloc-

ity by the expression
dθ
= 2 πf
dt (29.61)
Therefore, the average velocity is given by
*This argument is not compelling, because the logarithmic term is eventually expanded and only the
first term is used. This is equivalent to a linear rate of oxidation or of gas adsorption with time. A
linear rate of gas adsorption suggests that the amount of oxygen reaching the clean metal surface as
physically adsorbed gas may actually be controlling, rather than its conversion to chemisorbed oxygen
atoms. This possibility is given support by the observed increase of fretting weight loss as the tem-
perature is lowered, corresponding to increased rate and extent of physical adsorption at lower tem-
peratures. The rate of chemisorption, on the other hand, usually decreases as the temperature is
lowered.
DERIVATION OF THE EQUATION EXPRESSING WEIGHT LOSS 473
π
πlf ∫ sin θdθ
V=− 0
= 2lf (29.62)
π
Hence, for n contacts or asperities per unit area of interface, weight loss W per
cycle caused solely by oxidation is
Wcorr = 2 nlck ln ⎛ + 1⎞
s
(29.63)
⎝ 2lf τ ⎠
To this must be added loss of metal by wear because each asperity, on the
average, digs below the oxide layer and dissipates metal in an amount propor-
tional to the area of contact of the asperities and the length of travel. The area
of asperity, rather than the width, is important now because of the “tearing out”
or welding action taking place during mechanical wear, in contrast to scraping
off of chemical products from the surface, as discussed previously. A shearing
off of asperities without welding also leads to wear that depends on total area of
contact. For n circular asperities, weight loss per cycle is given by
( ) πl
2
c
Wmechanical = 2k ′n (29.64)
2
But nπ(c/2)2, the total area of contact, is equal [7] to the load L divided by the
yield pressure pm. The term pm is approximated by three times the elastic limit;
hence, for mild steel, pm equals 100 kg/mm2 or 140,000 psi.
Therefore,
lL
Wmechanical = 2k ′ = k2 lL (29.65)
pm
where k2 is a constant equal to 2k′/pm. The total wear or metal loss per cycle is
the sum of the oxidation, or corrosion, term and the mechanical term
Wtotal = Wcorr + Wmechanical (29.66)
Returning to (29.63), the logarithmic term can be expanded according to
x2 x3
ln( x + 1) = x − + −
2 3
where x is equal to s/(2lfτ). When the latter expression is much smaller than unity,
the square and higher terms can be omitted. This condition applies particularly
to high loads (small values of s), high-frequency f, and large value of slip l.
Empirical values of the constant τ for iron range from 0.06 to 3 s. Assuming
reasonable values for τ = 0.06 s, f = 10 cps, l = 0.01 cm, and s (distance between
474 APPENDIX
asperities) = 10−4 cm, then s/(2lfτ) = 0.008. Therefore, whenever experimental

conditions approximate those cited and higher terms of the logarithmic expan-
sion can be neglected, we obtain
ncks
Wcorr = (29.67)
fτ
This expression is equivalent to assuming, from the very start, a linear rate of
oxidation or of gas adsorption on clean iron, where k/τ is the reaction-rate con-
stant. The linear rate reasonably approximates the actual state of affairs for very
short times of adsorption or oxidation.
Since the number of asperities along one edge of unit area is equal to n , it
follows that s + c is approximated by 1/ n . Also, recalling that nπ(c/2)2 = L/pm,
the terms n, c, and s can be eliminated from (29.67), or
k0 L1/ 2 k1 L
Wcorr = − (29.68)
f f
where
2 k 4 k
k0 = and k1 =
pm π τ pm π τ
Combining (29.65), (29.66), and (29.68), we have the final expression for fretting
as measured by weight loss corresponding to a total of C cycles:
C
Wtotal = (k0 L1/ 2 − k1 L) + k2 lLC (29.69)
f
29.8 CONVERSION FACTORS
Multiply millimeters penetration per year (mm/y) by 2.74 × density (g/cm3) to

obtain grams per square meter per day (gmd).
Multiply gmd by 0.365/density to obtain mm/y.
Metal Density (g/cm3) 2.74 × Density 0.365/Density
Aluminum 2.70 7.40 0.135

Brass (red) 8.75 24.0 0.0417
Brass (yellow) 8.47 23.2 0.0431
Cadmium 8.65 23.7 0.0422
Columbium (niobium) 8.57 23.5 0.0426
Copper 8.96 24.6 0.0407
Copper–Nickel (70–30) 8.95 24.5 0.0408
Iron 7.87 21.6 0.0464
Iron–silicon (Duriron) (84–14.5) 7.0 19.2 0.0521
CONVERSION FACTORS 475
Metal Density (g/cm3) 2.74 × Density 0.365/Density

Lead (chemical) 11.35 31.1 0.0322
Magnesium 1.74 4.77 0.210
Nickel 8.90 24.4 0.0410
Nickel–copper (Monel) (70–30) 8.84 24.2 0.0413
Silver 10.49 28.7 0.0348
Tantalum 16.6 45.5 0.0220
Tin 7.30 20.0 0.0500
Titanium 4.51 12.4 0.0809
Zinc 7.13 19.5 0.0512
Zirconium 6.49 17.8 0.0562
Multiply inches penetration per year (ipy) by 696 × density to obtain milligrams
per square decimeter per day (mdd). Multiply mdd by 0.00144/density to obtain
ipy.
29.8.1 Additional Conversion Factors
Multiply by to obtain
ipy 25.4 mm/y

mdd 0.1 gmd
mA/cm2 10 A/m2
A/m2 0.093 A/ft2
psi 6.89 × 103 Pa (pascals)
Å 0.1 nm (nanometer)
29.8.2 Current Density Equivalent to a Corrosion Rate of 1 gmd
1 gmd = 1.117n / W amperes per square meter
where W is the gram atomic weighta
Reaction A/m2
Al → Al3+ + 3e− 0.124

Cd → Cd2+ + 2e− 0.0199
Cu → Cu2+ + 2e− 0.0352
Fe → Fe2+ + 2e− 0.0400
Fe → Fe3+ + 3e− 0.0600
Pb → Pb2+ + 2e− 0.0108
Mg → Mg2+ + 2e− 0.0919
Ni → Ni2+ + 2e− 0.0381
Sn → Sn2+ + 2e− 0.0188
Zn → Zn2+ + 2e− 0.0342
a
Multiply A/m2 by 0.1 to obtain mA/cm2.
476 APPENDIX
29.9 STANDARD POTENTIALS
25°C, see also Section 3.8.
φ° (volts)
FeO24 − + 8 H + + 3e − → Fe3 + + 4 H 2O 1.9

Co3+ + e− → Co2+ 1.82
PbO2 + SO24 − + 4 H + + 2e − → PbSO4 + 2 H 2O 1.685
NiO2 + 4H+ + 2e− → Ni2+ + 2H2O 1.68
Mn3+ + e− → Mn2+ 1.51
PbO2 + 4H+ + 2e− → Pb2+ + 2H2O 1.455
Cl2 + 2e− → 2Cl− 1.3595
Cr2O27 − + 14 H + + 6e − → 2Cr 3+ + 7 H 2O 1.33
O2 + 4H+ + 4e− → 2H2O 1.229a
Br2(l) + 2e− → 2Br− 1.0652
Fe3+ + e− → Fe2+ 0.771
O2 + 2H+ + 2e− → H2O2 0.682
I2 + 2e− → 2I− 0.5355
O2 + 2H2O + 4e− → 4OH− 0.401
Hg2Cl2 + 2e− → 2Hg + 2Cl− 0.2676
AgCl + e− → Ag + Cl− 0.222
SO24 − + 4 H + + 2e − → H 2SO3 +H 2O 0.17
Cu2+ + e− → Cu+ 0.153
Sn4+ + 2e− → Sn2+ 0.15
AgBr + e− → Ag + Br− 0.095
Cu(NH3)2+ + e− → Cu + 2NH3 −0.12
Ag(CN)−2 + e − → Ag + 2CN − −0.31
PbSO4 + 2e − → Pb + SO24 − −0.356
HPbO−2 + H 2O + e − → Pb + 3OH − −0.54
2H2O + 2e− → H2 + 2OH− −0.828
Zn(NH 3 )24 + + 2e − → Zn + 4 NH 3 −1.03
a
At pH 7, 0.2 atm O2, φ = 0.81 V.
Source: Data from Oxidation Potentials, W. Latimer, Prentice-Hall, Englewood Cliffs, NJ, 1952 (with
permission).
29.10 NOTATION AND ABBREVIATIONS
activity a
activity coefficient γ
ampere A
angstrom Å
atmosphere atm
atom percent at.%
calorie cal
NOTATION AND ABBREVIATIONS 477
centimeter cm
corrosion current Icorr
corrosion current density icorr
corrosion potential φcorr
corrosion potential of a galvanic couple φgalv
coulomb C
critical crack depth acr
current I
current density i
decimeter dm
density d
electromotive force (emf) E
equivalent eq
exchange current density i0
faraday F
foot ft
Flade potential φF
gallon gal
Gibbs free energy G
gram g
gram calorie cal
grams per square meter per day gmd
hour h
inch in.
inch penetration per year ipy
joule J
kilogram kg
kilometer km
liter L
mean ion activity coefficient γ±
megapascal MPa
meter m
microampere μA
micrometer (micron) μm
milliampere mA
milligram mg
milligrams per square decimenter per day mdd
milliliter mL
millimeter mm
millimeters penetration per year mm/y
millivolt mV
minute min
molal solution M
nanometer nm
normal solution N
478 APPENDIX
ohm Ω
ounce oz
overpotential η
overvoltage ε
parts per million ppm
pascal Pa
potential φ
potential on the standard hydrogen scale φH, φ(S.H.E.)
pound lb
pound per square inch psi
pressure p
relative humidity R.H.
saturated calomel electrode S.C.E.
second s
standard hydrogen electrode S.H.E.
stress-corrosion cracking S.C.C.
Tafel slope β
volt V
weight percent wt.%
yield strength Y.S.
REFERENCES
1. F. Mansfeld and K. Oldham, Corros. Sci. 11, 787 (1971); F. Mansfeld, in Advances in Cor-
rosion Science and Technology, Vol. 6, M. Fontana and R. Staehle, editors, Plenum Press,
New York, 1976, p. 163.
2. C. Wagner and W. Traud, Z. Elektrochem. 44, 391 (1938).
3. W. Langelier, J. Am. Water Works Assoc. 28, 1500 (1936).
4. C. Hoover, J. Am. Water Works Assoc. 30, 1802 (1938).
5. S. Powell, H. Bacon, and J. Lill, Eng. Chem. 37, 842 (1945).
6. F. Stone, in Chemistry of the Solid State, W. Garner, editor, Butterworths, London, 1955,
p. 385.
7. F. P. Bowden and D. Tabor, The Friction and Lubrication of Solids, Oxford University
Press, New York, 1950.
INDEX
KEY: T refers to tables. F refers to figures.
A vapor degreasing of, 293

Abbreviations, 476–478 waters, corrosion in, 384–386
Activity, coefficient: pH, effect of, 387
defi nition, 24 pitting, 98, 99
rules, 451–452 Aluminum alloys, 393–395
tables, 453–455 anodes in impressed current cathodic
Aircraft: protection, 259
aluminum alloys in, 395 clad, 384, 395
Boeing 777, 395 compositions, 385T
fretting corrosion, 182 exfoliation of, 394
hot corrosion, 229–230 intergranular corrosion, Al–Cu alloys,
microbiologically influenced corrosion, 393–394
388–389 sacrificial anodes, 254–255
stress-corrosion cracking, 395 stress-corrosion cracking, 384, 394–395
titanium, 425 Amorphous alloys, 335
Aluminum, 383–398 Amphoteric metals, 12, 47, 79, 245, 260, 279,
anodic protection, 446
anodizing, 287–288, 296 Anion, defi nition, 13
atmospheric corrosion, 194T, 383, 391 Anode:
cathodic protection of, 252, 260, 261, 384, defi nition, 11–13
395 materials, for cathodic protection, 258–260
chlorinated solvents, corrosion in, 389–391 sacrificial, 144, 251, 252, 254–257, 263, 354,
inhibitors for, 390 370, 378
mechanism of, 390–391 Anode–cathode area ratio, 56, 67–69, 71–75,
water, effect of, 390F 123, 132, 208–210
coatings, 280–281 magnesium, galvanic corrosion of, 402
corrosion characteristics, 384–392 tantalum, 442
by microbiological constituents in fuel, Anodic protection, 263–264
388–389 by alloying, 90–92
galvanic coupling of, 392–393 of aluminum, 264, 386
nitric acid, corrosion rates in, 392 theory of, 90–92
oxide coatings on, 287–288, 383, 386 Anodizing:
painting of, 296 aluminum, 287–288, 296
passivity of, 83, 383, 384, 386, 388 magnesium, 403
soil corrosion, 208 Atmospheric corrosion, 191–204
steam, corrosion in, 384 avoiding, 201–202

479
480 INDEX
comparison with seawater and soils, 195T Bridges, 2

corrosion product fi lms, protection by, cathodic protection for, 253
192–195 steel reinforcements in, 144
corrosion rates, steels, 193F failure by stress-corrosion cracking, 153,
alloying, effect of, 202T 169–170
various metals, 194T painting, 290
critical humidity, 199–200 weathering steels for, 201
factors influencing, 195–200 Bronzes, 13, 252, 270, 371–372
gases in atmosphere, effect of, 197–199
sulfur dioxide content of air, 197–198 C
moisture, effect of, 199–200 Cadmium, 70–71, 168, 178, 184, 198, 231, 264,
particulate matter, effect of, 196–197 271, 274, 276–277, 288, 314, 392–393,
time of wetness, 199 toxic properties of, 277, 392–393
types of atmospheres, 192 Catalytic properties and passivity, 108–109
Automobiles, 4, 196, 295 hydrogen overpotential, relation to, 65
aluminum alloys in, 394–395 Cathode, defi nition, 11–13
body panels: Cathodic protection, 251–267
electrogalvanizing, 270 anode materials for, 258–260
painting, 295 backfi ll, use of, 255, 259
phosphate coating, 287 coatings, combined use with, 255–257
engines, 3 criteria of protection, 260–263
Ford, 404 doubtful, 262
fretting corrosion, 182 potential measurements, 260–262
Honda, 395 current, magnitude required, 77–79,
lead in, 447 257–258
magnesium in, 399, 404 economics of, 263
nickel coatings, 272 history of, 252–253
mufflers, 2, 280 how applied, 253–254
painting, 295 overprotection, effect of, 259–260
stainless steels in, 341 pitting, used to avoid, 261–262, 354
Volkswagen, 399 potential decay along pipeline, 257
derivation of formula for, 467–469
B steel reinforcements in concrete, 144, 253
Backfi ll, for cathodic protection, 255, 259 stress-corrosion cracking, to avoid:
Bacteria, 4, 118–120, 206–207, 279, 298, 309, in aluminum alloys, 384, 395
367, 388–389 in brasses, 378
Blister, 66 in stainless steels, 360
Blister cracking, 170–172 in steel, 155–156, 162
Boiler corrosion, 323–330 in titanium alloys,
alkali addition, effect of, 327–328 theory of, 77–79
embrittlement detector, 324–325 Cation, defi nition, 13
inhibitors for, 328 Caustic embrittlement, 152
mechanisms of, 328–330 Cavitation-erosion, 130–131
oxygen, dissolved, effect of, 329 in diesel engine liner, 131F
oxygen scavengers, 318–319, 330 Cells:
Boiler water, treatment of, 326–328 Daniell, 54–55
alkali addition, 327–328 galvanic, 11–12, 22, 26, 54, 68, 84, 115, 143,
carbon dioxide removal, 326–327 157, 197, 207, 254, 280, 343, 369
inhibitor addition, 328 local-action, 10–11, 68, 142, 261
oxygen removal, 326 passive–active, 96, 280, 352
phosphate addition, 328 reference, 34–37
Brasses, 371–378 calomel, 35–36
naval, red, yellow, 371–372 copper–copper sulfate, 36–37
see also Copper–zinc alloys silver–silver chloride, 36–37
INDEX 481
types, in corrosion reactions, 13–15 atmospheric corrosion, 198

concentration, 13–14 seawater corrosion, 275
differential aeration, 13–15, 28–30, 164, 197, soil corrosion, 208
298–299, 329, 353, 370, 371, 384, 388, polarity reversal in hot waters, 276
430 see also Steel, galvanized
differential temperature, 14–15 organic, 289–301
dissimilar electrode, 13 cathodic protection, combined use with,
Cement, Portland, as cause of corrosion: 255–257
of aluminum, 388, 391 filiform corrosion, 296–299
of lead, 446 pigments, inhibiting, 291–292
as protective coating for steel, 286 plastic, 299–300
steel reinforcements, failure of, 143–145 prime coat, 291–292, 294, 295, 296, 299,
galvanic effects of, 144 requirements for, 291–292
Chromates, see Passivators rules for applying, 295
Chromium–iron alloys: surface preparation, 293–295
critical composition for passivity, 100–101 effect on life, 295T
critical current densities for passivity, 101F Cobalt and cobalt alloys, 419–423
oxidation, elevated temperatures, 232–235 cavitation-erosion, 420, 423
effect of yttrium, 234–235 compositions, 422T
maximum temperatures in air, 235T corrosion characteristics, 419–423
potentials of, in 4% NaCl, 101F fretting corrosion, 420, 423
Flade, 88F Cold working, effect on corrosion:
see also Stainless steels iron and steel, 149–150
Chromium–nickel alloys: nickel, 150
commercial alloys, composition, 413T pure iron, 150F
corrosion characteristics, 411–417 Complexes, chemical, effect on Emf, 30–32
critical composition for passivity, 102 Concrete, 143–145, 253, 388, 391
intergranular corrosion, 415 Condenser tube alloys, 378–379
oxidation, elevated temperatures, 226T, Converson factors:
236–237 corrosion rates, 474–475T
Clean Air Act, 191, 198, 289, 295 to current densities, 475T
Coatings: Copper, 367–381
compliant, 289 atmospheric corrosion, 194T, 195T, 197–199
inorganic, 285–288 blue staining, caused by, 321, 369
chemical conversion, 286–288 corrosion characteristics, 367–371
chromate, 288 deposit attack, 370
oxide, 287–288 hydrogen, reaction with, 231–232
phosphate, 286–287 impingement attack, 17, 368–372, 379, 411
as preparation for painting, 295–296 inhibitor for tarnish of, 314
Portland cement, 286 oxidation, high temperature, 230–232
vitreous enamel, 285–286 pitting of, 369–370, 371, 378
metallic, 269–283 seawater corrosion, 195T,
aluminum, 280–281 soil corrosion, 195T, 208, 209T
application, methods of, 269–271 stress-corrosion cracking, 371, 374
cadmium, 276–277 waters, corrosion by, 369–371
chromium, 279–280 Copper–nickel alloys, for condenser tubes,
classification, 271–272 378–379
lead, 274 see also Nickel alloys, copper–nickel,
nickel, 272–274 Copper–zinc alloys, 371–378
electroless, 273–274 dezincification, 17, 252, 334, 371–374
fogging of, 273 effect of Zn content, 372F
thickness of, 272–273 mechanism of, 334, 374
tin, 277–279 impingement attack, effect of Zn content,
zinc, 274–276 372F
482 INDEX
stress-corrosion cracking, 374–378 by ion-exchange resins, 326

effect of applied potential, 377F by sodium sulfite, 318, 326
effect of Zn content, 372F Dealloying, 17, 118, 172, 372–374
mercurous nitrate test, 376 Deaeration of water, 178, 317–319, 326, 402,
prevention, 378 414
Corrosion: defi nition, 319
alloying, effect of, 333–335 oxygen concentration, maximum allowable
cost, 2–5 for steel systems, 320T
current and corrosion rate, 56, 475T Depolarization:
importance of, 2–5 in acids, 124–125
direct and indirect losses, 2–5 by oxygen, 72, 116, 122, 124, 131–133, 139,
products, protective, in atmospheric 262, 458
corrosion, 192–195 Deposit attack, 370
rates, calculation of, from polarization data, Dezincification:
71–73, 456–461 Cu–Zn alloys, 334, 371–374
classification for handling chemical media, defi nition, 17
16 mechanism, 374
control of, anodic, cathodic, 68–69 Diesel engines, 130, 215, 322,
derivation of formula for, 456–461
polarization, influence on, 68–71 E
scientist and engineer, 1–2 Electrochemical equivalent, 10
tendency and free energy, 21–22 Electrochemical impedance spectroscopy,
types, 15–18 75–77
Corrosion-erosion, defi nition of, 17 Electrochemical mechanism:
Corrosion fatigue, 173–180 of corrosion, 9–18, 22, 70–71, 143
appearance of, 174 (Photo) for corrosion of iron and steel, 115–116
defi nition, 18, 173–174 of passivation, 89
effect of oxygen, moisture, 175 of pitting, 96, 351–353
mechanism of, 179–180 of stress-corrosion cracking, 157–158, 190,
minimum corrosion rate for, 178T 377
prevention, 178–179 Electrode:
strength, values of, 177T copper–copper sulfate, 36–37
Crazing, 286 hydrogen, 24–25
Crevice corrosion, 14, 29, 99, 117, 173, 342, oxygen, 28–30
350–351, 352–354, 361, 412, 416–417, reference, 34–38
429–430, 432 standard or normal hydrogen, 24–25
Critical pitting potential, 97–99, 160, 264, 351– Electron configuration theory, 102–108
354, 384–386, 421, 429, 437 Emf:
Critical pitting temperature, 99–100, 351–352 calculation of, 25–28
Crystal face, effect on corrosion, 13, 149 relation to Gibbs free energy, 22
effect on oxidation, 230–231, 232 Series, defi nition of, 30
Current density: Table, 31T
critical for passivity, 85–86, 90, 117, 242, 411 Endurance limit, 18, 141
for Cr–Fe alloys, 101F Environmental Protection Agency (EPA), 191,
for Ni–Cu alloys, 104F 196, 369, 447
exchange, 61 Exfoliation, 394
limiting, 58–60
passive, 85 F
for Ni–Cu alloys, 104F Faraday, value of, 22
Faraday’s law, 9–11, 56, 85, 178, 244, 259,
D Fatigue, affected by air, moisture, 175
Deactivation of water: limit, defi nition of, 18, 173
defi nition, 317 strength, defi nition of, 173
by hydrazine, 318–319 see also Corrosion fatigue
INDEX 483
Filiform corrosion, 279, 296–299 in natural waters and soils, 141–142

photos, 297 and passivity of stainless steels, 361
theory of, 298–299 Galvanic Series:
Films, oxide: defi nition, 32
isolation of, 94 in seawater, 33T
passive, oxidizing properties, 93–94 Galvanized steel, see Steel, galvanized
thickness of: Glass, cavitation–erosion, 130
on aluminum, 383 coatings, 256, 285–286
on iron, 93–94 electroless nickel coatings on, 274
Flade potential: stress-sorption cracking, 160
aluminum, 383 Glass electrode, 25
defi nition, 86 Glassy alloys, 335
chromium, 279 Gmd, conversion factors of mm/y,
chromium–iron alloys, 88F 474–475
iron, 47, 84–89, 93–94, 112 defi nition, 16
nickel, 410 Gold, 17, 22, 109, 227, 232, 269–270, 286, 334,
nickel–copper alloys, 106 372–374,
nickel–molybdenum alloys, 412 coatings, electrical contacts, 182
tantalum, 441 coupled to iron, 306
titanium, 426 fatigue, 175
Fogging, 16, 273, 411 Graphitic corrosion, 138, 142, 206
Fouling, marine: Gun barrels, protecting, 287
Cu 2+ concentration to prevent, 103–105, 252,
369 H
of Cu–Ni alloys, 103–105, 104F Humidity:
of stainless steel, 351 critical in atmospheric corrosion, 196,
Fracture mechanics, 162–166 199–201
Fretting corrosion, 180–184 and fi liform corrosion, 298
aircraft, 182 and growth of bacteria, 120
automobiles, 182 and stress-corrosion cracking, 165, 376
cobalt alloys, 420, 423 Hydrogen:
defi nition, 17, 180–181 cracking, 65–66, 166–172
equation for weight loss, 183 and cadmium coatings, 276
derivation of, 471–474 and cathodic protection, 252, 259, 267
factors causing, of steel of cobalt alloys, 421–423
mechanism, 182–184 mechanism, 167–170
nuclear reactors, 182 metal flaws, effect of, 170–172
prevention, 184 of stainless steels, 354–361
railroad car wheels, 182 of steel, 166–172
Fugacity, 24 of steel reinforcements in concrete,
Furnace windings, 236, 237 145
disease, in copper, 231–232
G in silver, 203
Galvanic coupling: electrode, 24–25, 25F
of aluminum, 391–393 standard, 25
in aerated media, 127 embrittlement, 54, 158, 166–169
in deaerasted media, 127–129 of aluminum alloys, 395
of different steels, 141–142 and cathodic protection, 259
in soils, 206 of magnesium alloys, 402
effects of, at elevated temperatures, 227–228 caused by microbiologically influenced
hydrogen cracking of stainless steels, caused corrosion, 118
by, 357 caused by pickling inhibitors, 312
hydrogen embrittlement of Ta, caused by, of Ta,
iron–gold, 306 of ultra-high-strength steels, 357
484 INDEX
overpotential, 60–61, 62T, 63–66, 70, 80–81, in vapor degreasing aluminum, 293
90, 116, 123, 125–129, 139, 143, 149– vapor phase, 201
150, 267, 278–279, 310, 402, 412, 448 see also Passivators
standard scale, defi nition of, 25 Insulation, stress-corrosion cracking
associated with, 355, 375
I Intergranular corrosion:
Impingement attack: in copper–zinc alloys, 156, 378
of condenser alloys, 379 defi nition, 17–18
of copper, 368–370 in aluminum alloys, 252, 384, 394, 395
of copper–tin alloys, 371 in high purity aluminum, 384
of copper–zinc alloys, 371–372 in lead alloys, 448
defi nition, 16–17 in nickel-base chromium alloys, 415, 416
photo, 368 in stainless steels, 252, 343–350, 358
Inhibition efficiency, defi nition, 311 in titanium, 430–431
Inhibitors, 2, 3, 303–316 in zirconium, 437
for aluminum, 384, 390, 392 Ion implantation, 270
classification, 303 Ionization constant of water, various
for corrosion fatigue, 178–179 temperatures, 28T
and critical pitting potential, 97 ipy, conversion factors to mdd, 474–475
defi nition, 303 defi nition, 16
for diesel-engine cylinder liners, 130 IR drop, 56–57, 63, 68, 73, 74, 88, 262–263,
for engine cooling systems, 323 456
evaluation of, 73 calculation of, in electrolytes, 58
in foods, 278 as cause of polarization, 61–63
for industrial waters, 318 Iron, 115–148
boiler waters, 152, 328 acids:
cooling waters, 322–323 citric, rates in, 71T, 139T
for iron and steel, 130, 133, 143 dissolved oxygen:
for lead, 447 effect of, 124–125
mechanism of, 304–308 inhibition by, 125–127
nontoxic, 323 HCl + NaCl, rates in, 139T
oxygen, as inhibitor in acids, 125 velocity, effect of, 125–127
in phosphate coatings, 287 anaerobic bacteria, effect of, 118–120
pickling, 310–313 anodic protection, 90, 263–264
applications of, 294, 312–313 atmospheric corrosion, 191–204
concentration, effect of, 312F cast,
hydrogen embrittlement, caused by, 312 coupled to steel, 142
pigments for paints, 291–292 graphitic corrosion, 138, 142, 206
slushing compounds, 313 soil corrosion, 138, 206
sodium: water pipe, 286
benzoate, 306, 384 in water, 138
borate, 133, 306, 322 composition, effects of, 138–142
polyphosphate, 306–307, 323 heat treatment, effect of, 142–143
silicate, 133 hydrogen cracking, 166–172
for soil corrosion, 206 delay time and H2 content, 168F
for stainless steels, 157, 361 metallurgical factors, effect of, 138–143
pitting corrosion, 350–351 oxidation, elevated temperatures:
for stress-corrosion cracking, of brass, 376, in oxygen, 232–234
378 in steam, 323–326
of steel, 152–156, 157 effect of pH, 327F
of stainless steels, 157 oxygen, dissolved, effect of, 116–118
of titanium alloys, 157, 430–431 pH, effect of, 120–123
for tarnishing of copper, 314 salts, dissolved, effect of, 131–138
toxicity, 303–304, 309 seawater, rates in, 124T, 195T
INDEX 485
soil corrosion, 205–213 corrosion characteristics:

stress, effect of cold work, 149–150 alloys, 400–403, 404–404
stress-corrosion cracking, 151–156 pure magnesium, 399–400
effect of: as sacrificial anode, 254–255
alkalies, 151–152 efficiency of, 255
carbon monoxide–carbon dioxide, 153 for hot water tanks, 256F
cold work, 153–155 stress-corrosion cracking, 402–403
illuminating gas (HCN), 153 tolerance limit, defi nition of, 400
liquid ammonia, 153 for iron, 401F
nitrates, 151–155 univalent ion, 259
silicates, 152 mdd, conversion factors to ipy, 474–475
temperature, effect of in aqueous media, defi nition of, 16
120 Molybdenum, 84, 96, 108, 184, 229, 237, 341–
velocity, effect of: 342, 344, 348, 350, 351, 353, 409T,
in acids, 125–127 412, 415–417, 421
in natural waters, 129–130
wrought, 123, 124T, 138, 206, 209T N
see also Steel Nernst equation, derivation of, 22–24
Nickel, 408–411
K atmospheric corrosion, 194T, 198–201
Knife-line attack, 348 corrosion characteristics, 408–411
Flade potential, 410
L oxidation, elevated temperatures, 216–217,
Lead, 445–449 236–237, 410
and air quality, 191 alloyed with Cr, 226T, 234F, 236–237
atmospheric corrosion, 192, 194T, 198 intergranular, 236–237, 410
cathodic protection of, 251, 260, 261, 262T, Nickel alloys, 411–417
chemical conversion coatings on, 286 compositions, 413T
coatings of, on steel, 179, 184, 271, 274 critical pitting potential, 98T
in copper alloys, 372 irradiation-assisted stress-corrosion
corrosion characteristics, 445–448 cracking, 172
of Pb-acid battery grids, 447–448 nickel–chromium, 236–237, 411–412
in differential temperature cells, 15 nickel–chromium–iron, 236, 414–415
fatigue cracks in, 174 in pressurized water reactors, 414–415
hydrogen overpotential of, 62T, 65 nickel–copper, 414
oxidation, 231 atmospheric corrosion, 194T
in paints, 290, 291–292, 295T, 296 cupro-nickel, 103, 378–379, 411
passivation of, 84, 92, 127 corrosion fatigue, 177T
polarization of, 68 in condenser tubes, 378–379
soil corrosion, 207, 208, 209T, corrosion in 3% NaCl, 103F
stray current corrosion, 242, 244T, 245 critical current densities, in 1N H2SO4, F
toxic properties of, 4, 393 fouling of, in seawater, 105
in water, 137, 317, 321, passive current densities, 104F
woods, corroded by, 446 passivity, 103–108
Lead and Copper Rule, EPA, 369, 447 pitting, in seawater, 104F
Liquid-metal embrittlement, 158, 160, 165 stress-corrosion cracking, 379
Local-action cells, 10–11, 68, 142, 261 nickel–molybdenum, 412, 415–416
current, 10, 259, 266 behavior in acids,
Luggin capillary, 56, 57F Nitrites, see Passivators
Nuclear reactors, 172–173, 182, 348, 437
M
Magnesium, 399–406 O
alloy compositions, 403T Overpotential:
coatings on, 403–404 defi nition, 60
486 INDEX
hydrogen, 60–61, 63–66 critical concentrations of chlorides and

factors affecting, 63–66 sulfates, 310T
mechanism of, 64–65 polyphosphate, 306–307, 323
values of, 62T combined with chromates, 309
metal deposition and dissolution, 61 for treatment of municipal waters, 321
values of, 62T disposal, 322
oxygen, 61 silicate, 133, 152, 306
values of, 44T for treatment of potable waters, 321–322
Overvoltage, theory of, 88–90, 304–308
defi nition, 60 toxicity, 303–304
Oxidation, 215–240 see also Inhibitors
catastropic, hot ash, 229 Passivity, 83–113
of copper, 230–232 of alloys, 100–108
equations expressing rate, 220–223 critical compositions, 100–102
galvanic effects, 227–228 breakdown of, 89, 90, 94, 96
initial, thin fi lm, 216–218 catalytic properties, relation to, 108–109
internal, 231 cathodic plolarization, effect of, 108
iron and iron alloys, 232–233 chlorides, action of, 96–100
iron–chromium alloys, 235–236 defi nitions, 84
life test, ASTM, 233–234 fi lm thickness:
nickel and nickel alloys, 236–237 on aluminum, 383
coupled to Pt in borax, 227–228 on iron, 93–96
reactive element effect, 215, 234–237 of iron:
Wagner theory, 223–224 in nitric acid, 89–90
Zn alloyed with Al, Li, 227T in sulfuric acid, 84–87
Oxidation-resistant alloys, 234–237 theories of, 92–96
Reactive element effect, 234–235 adsorption, 92–94, 96, 99, 102, 108
Oxides, properties, 224–227 electron configuration, 102, 108–109
p-, n-type, 224–225 oxide-film, 92, 96, 102
Patina, on copper, 198–199
P pH:
Paints, 289–291 aluminum, effect of, 387–388
applying, 295–296 defi nition, 28
see also Coatings, organic iron, effect of, 120–123
Parting, defi nition, 17, 334 measurement, 28
Passivators, 303–310 values for water at various temperatures,
applications, 308–310 28T
chromates, 303–310 zinc, effect of, 274–275
for cooling waters, 322–323 Pilling and Bedworth rule, 6, 219–220
toxicity, 304, 322–323 Pipelines, 2, 4
critical concentrations of chlorides and cathodic protection of, 211, 253–255, 257–
sulfates, 310T 263, 467–470
effect on steel, various temperatures and microbiologically influenced corrosion of,
Cl− concentrations, 308T 120
nontoxic alternatives, 323 hydrogen-induced cracking of, 140, 170
critical concentration, 305 inhibitors, 309
defi nition, 303 pitting of, 210
examples of, 88 soil corrosion of, 205, 206
oxygen as, 125, 306 stray-current corrosion of, 241–244, 247
sodium, benzoate, 306, 384 stress-corrosion cracking of, 153, 210–211,
borate, 133, 306, 322 300
nitrite, 303–306, 309–310 Pitting:
corrosion of steel, effect of in aluminum, 384–386
concentration, 309T in condenser alloys, 378–379
INDEX 487
in copper, 369–370 definition, 24

critical potential for, 97–99 standard hydrogen, defi nition, 25
critical temperature for, 99–100 Potentiometer, 22, 26, 66
defi nition, 16 Potentiostat, 66–67, 85, 263
elongated, 352, 353F Potentiostatic polarization, 85, 97, 105, 242
factor, 16 Pourbaix diagrams, 43–51
in stainless steels, 350–354 aluminum, 47–48, 383
theory of, 96–99, 351–353 basis of, 43–44
Plastics, coatings, used for, 299–300 copper, 367–368
tetrafluorethylene, 184, 300 iron, 45–47
Polarization: lead, 445–446
causes of, 58–63 limitations, 49
activation, 60–61 magnesium, 48–49, 400
concentration, 58–60 nickel, 408–410
IR drop, 61–63 tantalum, 441–442
corrosion rates: titanium, 419–420
anode–cathode areas: water, 44–45
effect of, 73–75 zirconium, 435–436
calculation of, 71–73
relation to, 68–71 R
defi nition, 54 Radiation damage, 172–173
galvanostatic, for iron, 86F Reaction limit, 334
how measured, 56–58 values, gold alloys, 334T
potentiostatic, for iron, 85F Reactive element effect, 215, 234–237
Potential: Resistivity:
calculation of, 22–28 IR drop in electrolytes, 58, 61–63
corrosion, 54 in soil, 206–207
definition, 56 measurement, 246
measurement, 66 formula for, derivation of, 470–471
critical: Ring-worm corrosion, 143
for pitting, 97–99 Risk, 5, 7–8
for stress-corrosion cracking, 158–162, Rust:
355–358 composition, 116
decay along pipeline: defi nition, 1
derivation of formula, 467–469 iron, effect on corrosion of, 14, 15F,
formula, 257 protection by, in atmospheric corrosion,
defi nition, 24–26 192–195, 201
drop along soil surface by current entering
pipe, 245, 469–470 S
Flade, chromium, value for, 279 Saturation index:
chromium–iron alloys, 88F alteration of, by water treatment, 136, 321
definition, 86 calculation of, 134–136, 417F
iron, value for, 86 derivation of equation for, 461–463
as calculated, 93, 112 effect of temperature, 136
in chromates, 88–89 limitations of, 137–138
nickel, value for, 410 and municipal waters, treatment of, 321–322
passivity, relation to stability of, 87 Schikorr reaction, 325
pH, dependence on, 86–87 Season cracking, 334–335
hydrogen, normal, 25 Seawater:
standard, 25 aluminum in, 280, 386, 392
liquid-junction, 33–34 galvanic coupling, 393
characteristic values, 34T cathodic protection in, 254–256, 258T, 261,
sign of, 25–28 272,
standard, 31T, 476T coal-tar coatings, 291
488 INDEX
copper–aluminum alloys in, 371 depth of burial, effect on, 207

copper–nickel alloys in, 378–379 factors affecting, 206–207
copper–zinc alloys in, 372 pitting, 208–210
corrosion of aircraft over, 229 rates, 195T, 209T
copper in, 195T, 369–370, resistivity measurements, 207, 246
corrosion in, 11, 14 stress-corrosion cracking, 210–211
corrosion rate of steel in, 16 Stainless steels, 335–365
corrosion rate of magnesium in, 19 anodic protection of, 90–91, 263–264
galvanic coupling in, 127 classes and types of, 337–343
galvanic series in, 32, 33F cold work, 343
IR drop in, 58 compositions, 338–340T
iron in, 118 corrosion resistance, general, 361–362
lead in, 446, 448 crevice corrosion, 350–351
lead alloys for cathodic protection, 446 avoiding, 354
magnesium in, 400, 405 defi nition, 100, 335
stress-corrosion cracking, 402 galvanic coupling, 357, 361
microbiologically influenced corrosion in, heat treatment, for optimum corrosion
118–119 resistance, 342–343
nickel in, 410, 411 sensitizing, 343
nickel–chromium alloys in, 412, austenitic, 343–345, 344F
nickel–chromium–iron alloy in, 414 ferritic, 349
nickel–chromium–molybdenum alloys in, history, 336–337
412, 416–417 hydrogen cracking, 167, 170, 357
nickel–copper alloys in, 103, 104F, 408T, avoiding, 361
411, 414 18–8, cold worked, 357
stainless steel in, 208, 341, 344, 350–351, galvanic coupling, as cause of, 167, 357
352, 353F, 354, 357, 360, 362 intergranular corrosion, 343–350
steel in, 123, 124T, 131–132, 138, 195T, austenitic types, 343–349
boiler corrosion, 324, 329 avoiding, 347–348
cavitation–erosion, 130 effect of carbon and nitrogen, 346F
corrosion fatigue, 175, 178 knife-line attack, 348
deaeration, 317 of nonsensitized alloys, 348–349
effect of carbon content, 139 theory of, 345–347
effect of chromium, 141, 208 ferritic types, 349–350
effect of flow velocity, 129, 130F theory of, 350
effect of nickel, 141 passivity, effect of alloyed Cu, Pt, Pd, 90
paints for, 292 pitting, 350–354
Portland cement coatings on, 286 avoiding, 354
and stray current corrosion, 244 critical potential, 97–99
titanium in, 98, 426, 429–430, 432 critical temperature, 99–100
titanium alloys in, 431 inhibiting against, 350–351
zinc in, 195T, 274–275 theory of, 351–353
zirconium in, 437 soils, corrosion in, 208
Sensitization: stress-corrosion cracking, hydrogen
aluminum alloys, 384, 393–394 cracking, 354–361
stainless steels, 156, 172, 343–347, 350, 351, austenitic:
359–361 avoiding, 360–361
Silver, 15, 16, 17, 32, 61, 179, 184, 197, 216, critical potential in MgCl2, 360
223–224, 227–228, 231, 232, 264, 269, damaging ions, 354–355
271, 334, 361, 400–402, 410, 447 in polythionic acids, 359–360
Slushing compounds, 313 metallurgical factors, 357–359
Soils, corrosion in, 205–213 nickel, effect of, 358F
avoiding, 211 nitrogen, carbon, effect of, 358, 359F
in cinders, 208 oxygen dissolved, effect of, 355, 356F
INDEX 489
ferritic and martensitic, 354, 356–357, 361 avoiding, 246–247

weld decay, 344, 345F damage by, ac vs. dc, 241–242
Steam: to amphoteric metals, 245
condenser corrosion, 327 quantitative values, 244
corrosion: detection of, 245
of aluminum in, 386 pipe, inside of, 243–244
of iron in, 323–326 sources of, 242–244
of zirconium in, 437–438 Stress, residual, 149
return-line corrosion, 327, 328 in brass, 376
Steel: and corrosion fatigue, 177
atmospheric corrosion, 193F, 194T, 195T, and hydrogen-induced cracking, 170
202T in magnesium alloys, 402–403
Bessemer, oxygen-furnace, 138 in stainless steels, 357
carbon content, effect on corrosion, in 3% and stress-corrosion cracking of steel, 151,
NaCl, 124T 155, 156T
in hydrochloric acid, 151 in zirconium alloys, 437
in seawater, 139 Stress-corrosion:
cold rolling, effect of, 149–150 of aluminum alloys, 394–395
composition, effects of, 138–141 of bridge cable, 153
corrosion fatigue, 173–180 of copper–zinc alloys, 162, 163F, 374–379
fretting corrosion, 180–184 critical crack depth, 165–166
galvanic coupling, effects of, 141–142 defi nition, 18
galvanized, 274–276 initiation of, critical potentials for,
corrosion of: 161–162
atmospheric, 198, 274, 275T of iron and steel, 151–156
in soils, 206, 208, 209T of magnesium alloys, 402–404
first patent, 252 mechanisms, 156–166
painting of, 296 of pipelines, 210–211
pitting of, in hot water, 276 rate of crack growth, 162–166
heat treatment, effect on corrosion, in water, of stainless steels, 354–361
124T surface flaws, effect of, 166, 431
in acids, 143 of titanium alloys, 431
low alloy, 138–142, 206 Stress intensity factor, 164–166, 171–172
atmospheric corrosion, 193F, 194T, 201 Stress-sorption cracking, 158–161, 395
copper-bearing, 124T, 140–141, 206 Subscale formation, 231
atmospheric corrosion, 193F, 202T Sulfidation, 18, 226, 230, 237, 409T
corrosion in aqueous media, 123, Sulfide stress cracking, 166–167, 421
138–142 effect of surface flaws, 171–172
corrosion fatigue, 177T
oxide coatings on, formation of, 287 T
pickling of, 294 Tafel equation, 61, 64, 71, 457, 459
reinforcements in concrete, 143–145 Tantalum, 441–443
cathodic protection, 144, 253 as alloying element, 155
soils, corrosion in, 206, 207, 208, 209T, corrosion characteristics, 436, 441–443
210 galvanic effect, 227, 228F
stress-corrosion cracking in, 210–211 and glass coatings, 286
stainless, see Stainless steels hydrogen embrittlement, avoiding, 441–442
weathering, 201 passivity, 96, 441–442
see also Iron Telluric currents, 241
Stepwise cracking, 140, 166 Terne plate, 274
Stern–Geary equation, 72–73 Thermal spraying, 270
derivation of, 456–458 Tin:
general corrosion, 458–461 atmospheric corrosion, 194T
Stray-current corrosion, 241–249 coatings, 277–279
490 INDEX
complexes, effect on corrosion, 30–32 Water, treatment of, 317–332

corrosion characteristics, 279 boiler, 323–328
Titanium, 425–434 cooling, 322–323
alloy compositions, 428 hot-water heating systems, 321–322
corrosion characteristics, 425–432, 436 municipal supplies, 321–322
in alkali–hydrogen peroxide solution, 427 Welds:
Flade potential, 426 knife-line attack, 348
hydrochloric acid, corrosion rates in weld decay, 345 (Photo)
inhibited, 427–429, 428F definition, 344
effect of alloyed Pt or Pd, 428F
nitric acid, fuming, reaction with, 427 Y
pitting and crevice corrosion, 429–430 Yttrium, 215, 234–235, 236–237, 271
in bromides, iodides, 429–430
pitting potentials in chlorides at elevated Z
temperatures, 430F Zinc:
seawater, resistance to, 429–430 atmospheric corrosion, 194T, 195T, 198, 199
stress-corrosion cracking of alloys, 431 chromate coatings on, 288
cathodic protection against, 431 coatings on steel, 208, 274–276. see also
inhibiting ions for, 431 Steel, galvanized
Transition metals: electrogalvanizing, 270
catalytic properties, 108–109 oxidation of, in O2 , 227T
overpotential for deposition or dissolution, painting of, 296
61 pH, effect of, 275F
passive properties, 93 -rich paints, 292, 296
Transpassivity, defi nition, 92 seawater corrosion, 195T, 275
Tungsten, 96, 220, 221, 412, 421, soil corrosion, 195T, 207, 208, 209T, 211
Zirconium, 435–440
V corrosion characteristics, 435–439
Valves, corrosion of, 142 pitting in chlorides, critical potentials for,
Vanadium, as cause of catastrophic oxidation, 437
229 Pourbaix diagram, 436
radiation, effect on, 173
W steam, behavior in, 437–438, 439F
Wagner: effect of alloyed tin, 438
defi nition of passivity, 84 stress-corrosion cracking, 437
theory of oxidation, 223–224 transition point, 436, 438, 439F
and Traud experiment, 70 water, high temperature, corrosion by,
Wash primer, 296 437–439

Corrosion and Corrosion Control, 4th Ed

Uploaded by

Copyright:

Available Formats

Corrosion and Corrosion Control, 4th Ed

Uploaded by

Document Information

Copyright

Available Formats

Share this document

Share or Embed Document

Sharing Options

Did you find this document useful?

Is this content inappropriate?

Copyright:

Available Formats

Corrosion and Corrosion Control, 4th Ed

Uploaded by

Copyright:

Available Formats

CORROSION AND

A JOHN WILEY & SONS, INC., PUBLICATION

A JOHN WILEY & SONS, INC., PUBLICATION

Published by John Wiley & Sons, Inc., Hoboken New Jersey

Library of Congress Cataloging-in-Publication Data:

Uhlig, Herbert Henry, 1907–

Printed in the United States of America

1 DEFINITION AND IMPORTANCE OF CORROSION 1

3 THERMODYNAMICS: CORROSION TENDENCY AND

4 THERMODYNAMICS: POURBAIX DIAGRAMS 43

5 KINETICS: POLARIZATION AND CORROSION RATES 53

5.11 Theory of Cathodic Protection 77

7 IRON AND STEEL 115

7.3.3 Effect of Heat Treatment 142

8 EFFECT OF STRESS 149

9 ATMOSPHERIC CORROSION 191

9.3 Corrosion-Product Films 192

10 CORROSION IN SOILS 205

11.13.2 Chromium–Iron Alloys 235

12 STRAY-CURRENT CORROSION 241

13 CATHODIC PROTECTION 251

14 METALLIC COATINGS 269

15 INORGANIC COATINGS 285

16 ORGANIC COATINGS 289

17 INHIBITORS AND PASSIVATORS 303

18 TREATMENT OF WATER AND STEAM SYSTEMS 317

19 ALLOYING FOR CORROSION RESISTANCE;

19.2.7 Galvanic Coupling and General Corrosion

20 COPPER AND COPPER ALLOYS 367

21 ALUMINUM AND ALUMINUM ALLOYS 383

22 MAGNESIUM AND MAGNESIUM ALLOYS 399

23 NICKEL AND NICKEL ALLOYS 407

24 COBALT AND COBALT ALLOYS 419

26.3 Behavior in Hot Water and Steam 437

29.9 Standard Potentials 476

Indeed, this remains the main objective today.

Ottawa, Canada R. Winston Revie

1.1 DEFINITION OF CORROSION

Corrosion is the destructive attack of a metal by chemical or electrochemical

1.1.1 Corrosion Science and Corrosion Engineering

Corrosion and Corrosion Control, by R. Winston Revie and Herbert H. Uhlig

electrochemistry is also important. Furthermore, since structure and composition

1.2 IMPORTANCE OF CORROSION

1. Shutdown. The replacement of a corroded tube in an oil reﬁnery may cost

may damage an entire batch of soap. Copper salts accelerate rancidity of

1.3 RISK MANAGEMENT

In general, risk, R, is deﬁned as the probability, P, of an occurrence multiplied by

4 Extreme Risk. Extensive risk

3 High-Consequence Risk. Risk

A B C D Low Risk. Risk controls may be

1.4 CAUSES OF CORROSION

1.4.1 Change in Gibbs Free Energy

1.4.2 Pilling–Bedworth Ratio

1. Gerhardus H. Koch, Michiel P. H. Brongers, Neil G. Thompson, Y. Paul Virmani, and J. H.

Materials Performance, July 2002, Report No. FHWA-RD-01-156, Federal Highway

R. Bhaskaran, N. Palaniswamy, N. S. Rengaswamy, and M. Jayachandran, Global cost of

1. A manufacturer provides a warranty against failure of a carbon steel product

(a) Calculate the risk of failure by corrosion, in dollars.

2.1 THE DRY-CELL ANALOGY AND FARADAY’S LAW

As described in Chapter 1, corrosion processes are most often electrochemical.