The Role Stainless Steel in Industrial Heat Exchangers

The Role
Stainless Steel in Industrial

Heat Exchangers
1
CONTENTS
Stainless Steel 2
Choosing the Right Stainless Steel 6
Corrosion Resistance 6
Cooling Water Conditions 11
Contamination 12
Versatility of Stainless Steels 12
High-Temperature Resistance 14
Low-Temperature Resistance 16
Heat Transfer Properties 17
Cleanliness 20
Design Versatility 20
Stainless Steels Are Economical 27
Installation and Maintenance 28
Applications
Pulp and Paper 30
Food Processing 32
Nitric Acid 33
High-Temperature Recuperators 35
Stator Cooling 38
Sulfuric Acid Production 38
Petroleum Refining 39
Acetic Acid 41
Synthetic Natural Gas 43
References 44
2
Many industrial and chemical processes involve heating and cool-
ing. Since heat represents money, heat exchangers are an extremely
vital part of the process equipment.
The amount of stainless steel utilized in heat exchange equipment
is increasing as industry strives toward greater efficiency and reduced
costly shutdowns in its operations and higher product purity. As will be
shown, stainless steel is sometimes the only material that can be used;
in other situations it is the most economical when costs of installation,
maintenance and production stoppages are considered.
Following are ten good reasons for using stainless steels in heat
exchange equipment:
1. Resistance to Corrosion in
Virtually all cooling waters and
Many chemical environments
2. High-Temperature Resistance to Oxidation and Scaling
3. Good Strength Characteristics in Low- and High-Temperature
Service
4. Maintains Excellent Heat Transfer Properties in Service
5. Resistance to Fouling Due to Corrosion
6. No Contamination of Product or Process by Corrosion
7. Easy to Clean Mechanical Chemical
8. Fabricability
9. Availability in a Variety of Compositions as
Seamless & welded tubing for shell-and-tube exchangers
Thin flat-rolled sheet & strip for plate exchangers
Plate for tubesheets
Bar and wire for mechanical fasteners
10.Economical-in Terms of
First cost
Long-term service

STAINLESS STEEL

Stainless steels are iron-base alloys containing a minimum of
10.5% chromium. There are 57 separate and distinct commercial com-
positions designated by American Iron and Steel Institute as standard
types. Fifteen of the most widely used types in heat exchange service
are listed in Table 1 along with their chemical compositions and prop-
erties. A complete listing of all standard AISI types and a description
of each are contained in the AISI publication, Steel Products Manual
Stainless and Heat-Resisting Steels.
1

In addition to the standard AISI types, many special-analysis and
proprietary stainless steels are produced in the United States and
Canada. Many of these are identified in technical literature, such as
in the ASTM Data Series Booklet DS 45.
2

AISI stainless steels are identified by a system of numbers that are
in either 200, 300, or 400 Series. In addition, all are identified by the
new Unified Numbering System (UNS) which has been developed for all
commercial metals and rare earths. For example, Type 304 is S30400 in
UNS. Special analysis and proprietary alloys may have numbers that
resemble AISI type numbers. To avoid confusion, the term alloy will be
used in this publication in referring to stainless steels other than the
AISI compositions.
The terms austenitic, martensitic, ferritic and precipitation harden-
3
ing serve to identify categories of stainless steels on the basis of their
metallurgical structure. Engineers should recognize these terms and
understand what they mean, because stainless steels so classified tend
to have similar characteristics with respect to corrosion resistance,
hardenability, and fabricability.

Austenitic
Austenitic stainless steels are chromium-nickel-manganese and
chromium-nickel compositions, which can be hardened only by cold
working; heat treatment serves only to soften them. They are nonmag-
netic in the annealed condition, although some may become slightly
magnetic after cold working.
The austenitic group of stainless steels is characterized as having
excellent corrosion resistance, unusually good formability, and the ability
to develop high strength. In the annealed condition, they possess
maximum ductility, good yield and tensile strength, high impact strength,
and good notch toughness.
Typical of this group is Type 304, also widely known as 18-8 stain-
less, a general-purpose stainless steel. There are numerous composi-
tions in this group. In these variations, (1) the chromium/nickel ratio has
been changed to improve the forming characteristics (Types 301 and
305), (2) the carbon content has been decreased to prevent carbide
precipitation in weldments (Types 304L, 316L, and 317L), (3) titanium or
columbium has been added to prevent carbide precipitation resulting
from exposure to high temperature (Types 321 and 347), (4) molybdenum
has been added or the chromium and nickel contents have been in-
creased to improve corrosion or oxidation resistance (such as Types 316
and 317 with molybdenum, and 309 and 310 with higher alloy content),
and (5) sulfur or selenium has been increased or added to improve
machining characteristics (Types 303 and 303 Se).
The 200 Series stainless steels (Types 201, 202, and 205) are very
similar to the 300 Series types except that manganese replaces some of
the nickel, and these alloys have higher yield and tensile strengths.

Ferritic
The ferritic stainless steels are identified by 400 Series numbers.
These straight-chromium alloys are not hardenable by heat treatment and
only slightly hardenable by cold working. They are magnetic, have good
ductility and good resistance to corrosion and oxidation. Typical of this
group is Type 430, with nominally 17% chromium. Among the several
variations in the ferritic group, two have increased chromium content to
improve scaling resistance (Types 442 and 446).

Duplex (Ferritic/Austenitic)
Some stainless steels, such as Type 329, cannot be classified
strictly as austenitic, ferritic, or martensitic because of a two-phase
structure consisting of a ferritic matrix with pools of austenite. In addition
to good general corrosion resistance, comparable to that of Type 316
stainless steel, the ferritic/austenitic alloys have high resistance to
stress-corrosion cracking.

Martensitic
The martensitic stainless steels are straight-chromium steels having
a carbon/chromium ratio higher than that of the ferritic group. Con-
sequently, they can be hardened by heat treatment.
These stainless steels resist corrosion in mild environments (atmos-
4
TABLE 1 Stainless Steel Properties

Chemical Analysis %
(Max unless noted otherwise)

304
(S30400)

304L
(S30403)

309S
(530908)

310S
(S31008)

316
(S31600)

316L
(S31603)

317
(S31700)

317L
(S31703)
Carbon 0.08 0.030 0.08 0.08 0.08 0.030 0.080 0.030
Manganese 2.00 2.00 2.00 2.00 2.00 2.00 2.00 2.00
Phosphorus 0.045 0.045 0.045 0.045 0.045 0.045 0.045 0.045
Sulfur 0.030 0.030 0.030 0.030 0.030 0.030 0.030 0.030
Silicon 1.00 1.00 1.00 1.50 1.00 1.00 1.00 1.00
Chromium 18.00/20.00 18.00/20.00 22.00/24.00 24.00/26.00 16.00/18.00 16.00/18.00 18.00/ 20.00 18.00/20.0
Nickel 8.00/10.50 8.00/12.00 12.00/15.00 19.00/22.00 10.00/14.00 10.00/14.00 11.00/15.00 11.00/15.010
Molybdenum 2.00/ 3.00 2.001 3.00 3.00/ 4.00 3.00/ 4.0
0
)
Other

Physical Constants
Structure Austenitic Austenitic Austenitic Austenitic Austenitic Austenitic
Magnetic No No No No No No
Density Ibs/in
3
(k/m') 0.29 (80(x0) 0.29 (8060) 0.29 (8060) 0.29 (8060) 0.29 (8060) 0.29 (8060)
Specific Heat Btu/ Ib/F
(1/kg-K) 32 to 212 F (0-100 C)

0.12 (503)

0.12 (503)

0.12 (503)

0.12 (503)

0.12 (503)

0.116 (486)
Thermal Conductivity Btu/ hr/ft
2
/ft/F
(W/ m-K) 212 F (100 C)
932 F (500 C)

9.4(0.113)
12.4 (0.149)

9.0 (0.108)
10.8 (0.130)

8.2 (0.099)
10.8 (0.130)

9.4(0.113)
12.4 (0.149)

9.4 (0.113)
12.4 (0.149)

8.3 (0.100)

Mean Coefficient of Thermal
Expansion
10
6
/F (10
6
/C)
32 to 212 F (0-100 C)
32 to 600 F (0-315 C)
32 to 1000 F (0-538 C)
32 to 1200 F (0-648 C)
32 to 1800 F (0-982 C)

9.6 (17.3)
9.9(17.9)
10.2 (18.4)
10.4 (18.8)

8.3 (15.0)
9.3 (16.6)
9.6 (17.2)
10.0 (18.0)
11.5 (20.6)

8.8 (15.9)
9.0 (16.2)
9.4 (17.0)
9.7 (17.5)
10.6 (19.1)

8.9 (15.9)
9.0 (16.2)
9.7 (17.5)
10.3 (18.6)
11.1 (20.0)

8.9 (16.0)
9.0 (16.2)
9.7 (17.5)
10.3 (18.6)
11.1 (20.0)

9.2 (16.5)
10.1 (18.1)
10.3 (18.6)

Tensile Modulus of Elasticity
psi X 10
6
(GPa)

28.0 (193)

29.0 (200)

29.0 (200)

28.0 (193)

28.0 (193)

29.0 (200)
Torsional Modulus of Elasticity
psi X 10
6
(GPa)

12.5 (86.2)

Melting Point Range F
(C)

2550-2650
(1398-1454)

(
S
i
m
i
l
a
r

t
o

T
h
o
s
e

o
f

T
y
p
e

3
0
2
)

2550-2650
(1398-1454)

2550-2650
(1398-1454)

2500-2550
(1371-1398)

(
S
i
m
i
l
a
r

t
o

T
h
o
s
e

o
f

T
y
p
e

3
1
6
)

2500-2550
(1371-1398)

2500-2550
(1371-1398)

Typical Mechanical Properties
(annealed condition)
Stainless Steel Sheet

Tensile Strength
ksi (MPa)

84(579)

81 (558)

90(621)

95 (655)

84(579)

81 (558)

90 (621)

86 (593)
Yield Strength (offset 0.2%)
ksi (MPa)

42(290)

39(269)

45(310)

45(310)

42(290)

42(290)

40(276)

38(262)
Elongation in 2" % 55 55 45 45 50 50 45 55
Reduction of Area %
Izod Impact Strength
ft-Ib-force (J)

Hardness (Rockwell)

B80

B79

B85

B85

B79

B79

B85

B85

5

321
(532100)

329
(S32900)

347
(S34700)

348
(534800)

410
(S41000)

430
(S43000)

446
(544600)
0.08 0.10 0.08 0.08 0.15 0.12 0.20
2.00 2.00 2.00 2.00 1.00 1.00 1.50
0.045 0.040 0.045 0.045 0.040 0.040 0.040
0.030 0.030 0.030 0.030 0.030 0.030 0.030
1.00 1.00 1.00 1.00 1.00 1.00 1.00
17.00119.00 25.00/30.00 17.00119.00 17.00/19.00 11.50/13.50 16.00/18.00 23.00/27.OC
9.00/12.00 3.00/ 6.00 9.00/13.00 9.00; 13.00
1.001 2.00
Ti (5 X C Min.)

Cb + Ta (10 X C Min.)

Cb + Ta (10 X C Min.)
Ta 0.10 Co 0.20

Austenitic Austenitic-Ferritic Austenitic Martensitic Ferritic Ferritic
No No No Yes Yes Yes
0.29 (8060) 0.28 (7780) 0.29 (8060) 0.28 (7780) 0.28 (7780) 0.27 (7550)
0.12 (503) 0.11 (460) 0.12 (503) 0.11 (460) 0.11 (460) 0.12 (502)
9.3 (0.112)
12.8 (0.154)

9.3 (0.112)
12.8 (0.154)
14.4 (0.174)
16.6 (0.201)
15.1 (0.182)
15.2 (0.183)
12.1 (0.146)
14.1 (0.170)

9.3 (16.6)
9.5 (17.2)
10.3 (18.6)
10.7 (19.3)
[to 1700] 11.4 (20.6)

[to 1500] 8.0 (14.4)

9.3 (16.6)
9.5(18.2)
10.3 (18.6)
10.6 (19.1)
[to 1500] 11.1 (20.0)

5.5 (9.9)
6.3 (11.4)
6.4 (11.6)
6.5 (11.7)

5.8 (10.4)
6.1 (11.0)
6.3 (11.4)
6.6 (11.9)
[to 1500] 6.9 (12.4)

5.8 (10.4)
6.0 (10.8)
6.2 (11.2)
6.4 (11.6)
6.7 (12.1)
28.0 (193) 28.0 (193) 29.0 (200) 29.0 (200) 29.0 (200)

2550-2600
(1398-1427)

2550-2600
(1398-1427)

(
S
i
m
i
l
a
r

t
o

T
h
o
s
e

o
f

T
y
p
e

3
4
7
)

2700-2790
(1483-1532)

2600-2750
(1427-1510)

2600-2750
(1427-1510)

90(621)

105 (724)

95(655)

95(655)

70(483)

75(517)

80(552)
35(241) 80(552)
40(276)

40(276)

45 (310)

50(345)

50(345)

45 25 45 45 25 25 20
50

40(54)

B80

(Brinell 230)

B85

885

B80

B85

B83

6
phere, fresh water, weak acids, etc.). They have fairly good ductility and
are always strongly magnetic. There are 12 compositions in this group,
with Type 410 being the most common. Type 410 with 12% chromium is
used for heat exchange service, but its carbon content is reduced to
minimize hardenability.

Precipitation Hardening
Precipitation hardening stainless steels are hardened by a low-
temperature aging treatment in combination with cold working. They
are rarely used in heat exchange applications.

CHOOSING THE RIGHT STAINLESS STEEL

Selection of the right stainless steel from the many types available
requires an evaluation based upon four important criteria. Listed in
order of descending importance, they are:
Corrosion Resistance
3
the primary reason for specifying stain-
less steel. The specifier needs to know the nature of the environ-
ment and the degree of corrosion resistance required.
Cost PerformanceTo put everything into proper perspective, a
total value analysis is appropriate. How much is it going to cost
spread over the entire service life? This considers first cost plus
savings in maintenance and replacement.
Fabricabilityand how the product is to be made is a third-level
consideration. This includes ability to be welded, formed, etc.
Mechanical Propertieswith particular emphasis on heat transfer
characteristics and on strength at ambient, elevated, or low tem-
perature. Generally speaking, the combination of corrosion resist-
ance and strength is the basis for selection.

CORROSION RESISTANCE

Corrosion has always been an important and costly problem facing
the process engineer. The decision as to whether a chemical process is
practical or not is intimately related to the corrosivity of the process. Not
only must equipment damage and repair under corrosive attack and
subsequent repair be considered, but the danger of product loss or
contamination must be eliminated.
The presence of chromium in all stainless steels is chiefly respon-
sible for their resistance to corrosion. With 10.5% or more chromium
(Figure 1) a protective oxide film forms under normal atmospheric con-
ditions. As the chromium content is increased, resistance to corrosion
also increases so that stainless containing 17% chromium has improved
corrosion resistance, and stainless steel containing 28% chromium is
even more corrosion resistant.
Passivity, the mechanism by which the stainless steels derive their
corrosion resistance, has been a popular subject for electrochemical
research for many years. This phenomenon is difficult to define because
of its complex nature and the specific conditions under which it occurs.
Essentially, passivity implies a loss of chemical reactivity experienced
by certain metals and alloys under particular environmental conditions.
For the purpose of this discussion, passivity in stainless steels is gen-
erally understood to be related to the thin transparent oxide film that
creates a protective barrier between the stainless steel and its environ-
7
Figure 1
Source: Stainless Steel Industry Data
ment. This film is self-forming and exists on all clean stainless steel
alloys. Although this barrier film has been studied for many years, its
exact nature is still not known. However, it has been established that
chemically oxidizing media are necessary for film formation and repair.
Consequently, the fact that stainless steels perform well in oxidizing
environments is well founded in corrosion theory.
As oxidizing media are needed to maintain stable passivity, con-
versely the stainless steels give relatively poor performance in reducing
environments. Dilute sulfuric and hydrochloric acids are typical of such
environments, and are quite corrosive to stainless steels, particularly at
elevated temperatures. The corrosive attack experienced is an
instantaneous breakdown of the passive film resulting in general dis-
solution accompanied by the evolution of hydrogen gas.
Some ions, particularly the halogens, are capable of causing local-
ized breakdown of the passive film. When this occurs under conditions
where film repair is impossible or delayed, pitting attack can occur.
When stainless steel contains nickel as well as chromium, ductility,
toughness and strength at elevated temperatures are increased. Some
improvement in corrosion resistance may also occur.
Stainless steels containing molybdenum (such as Type 316) offer
improved resistance over that of Type 304 to chemical agents that
cause pitting corrosion, such as chlorides, photographic solutions,
sulfite liquors, and hypochlorites.
Table 2 suggests various corrosive environments in which stainless
steels are used for heat exchangers and other process equipment.
4
Also,
appearing throughout this publication are more detailed descriptions of
specific heat exchanger applications and materials experiences in such
industries as pulp and paper, food, LNG, SNG, ntiric acid, sulfuric acid,
acetic acid, and petroleum refining.
8
TABLE 2
Where Different Grades Are Used
4

Environment Grades

Acids
Hydrochloric acid

Stainless generally is not recommended except
when solutions are very dilute and at room
temperature.
Mixed acids There is usually no appreciable attack on Type 304
or 316 as long as sufficient nitric acid is present.
Nitric acid Type 304L or 430 is used.
Phosphoric acid Type 304 is satisfactory for storing cold phosphoric
acid up to 85% and for handling concentrations up
to 5% in some unit processes of manufacture. Type
316 is more resistant and is generally used for stor-
ing and manufacture if the fluorine content is not
too high. Type 317 is somewhat more resistant than
Type 316. At concentrations up to 85%, the metal
temperature should not exceed 212 F (100 C) with
Type 316 and slightly higher with Type 317. Oxidiz-
ing ions inhibit attack and other inhibitors such as
arsenic may be added.
Sulfuric acid Type 304 can be used at room temperature for con-
centrations over 80%. Type 316 can be used in
contact with sulfuric acid up to 10% at tempera-
tures up to 120 F (50 C) if the solutions are aerated;
the attack is greater in airfree solutions. Type 317
may be used at temperatures as high as 150 F (65 C)
with up to 5% concentration. The presence of other
materials may markedly change the corrosion rate.
As little as 500 to 2000 ppm of cupric ions make it
possible to use Type 304 in hot solutions of moder-
ate concentration. Other additives may have the op-
posite effect.
Sulfurous acid Type 304 may be subject to pitting, particularly if
some sulfuric acid is present. Type 316 is usable at
moderate concentrations and temperatures.
Bases
Ammonium hy-
droxide, sodium
hydroxide, caustic
solutions
Steels in the 300 series generally have good corro-
sion resistance at virtually all concentrations and
temperatures in weak bases, such as ammonium
hydroxide. In stronger bases, such as sodium hy-
droxide, there may be some attack, cracking or
etching in more concentrated solutions and at high
er temperatures. Commercial purity caustic solu-
tions may contain chlorides, which will accentuate
any attack and may cause pitting of Type 316 as
well Type 304.
Organics
Acetic acid
Acetic acid is seldom pure in chemical plants but
generally includes numerous and varied minor con-
stituents. Type 304 is used for a wide variety of
equipment including stills, base heaters, holding
tanks, heat exchangers, pipelines, valves and pumps
for concentrations up to 99% at temperatures up to
about 120 F (50 C). Type 304 is also satisfactory for
contact with 100% acetic acid vapours, and-if
small amounts of turbidity or color pickup can be
toleratedfor room temperature storage of glacial
acetic acid. Types 316 and 317 have the broadest
range of usefulness, especially if formic acid is also
present or if solutions are unaerated. Type 316 is

Environment Grades

used for fractionating equipment, for 30 to 99%
concentrations where Type 304 cannot be used, for
storage vessels, pumps and process equipment
handling glacial acetic acid, which would be dis-
colored by Type 304. Type 316 is likewise applicable
for parts having temperatures above 120 F (50 C),
for dilute vapours and high pressures. Type 317 has
somewhat greater corrosion resistance than Type
316 under severely corrosive conditions. None of
the stainless steels has adequate corrosion resist-
ance to glacial acetic acid at the boiling tempera-
ture or at superheated vapour temperatures.
Aldehydes Type 304 is generally satisfactory.
Amines Type 316 is usually preferred to Type 304.
Cellulose acetate Type 304 is satisfactory for low temperatures, but
Type 316 or Type 317 is needed for high tempera-
tures.
Citric, formic and
tartaric acids
Type 304 is generally acceptable at moderate tem
peratures, but Type 316 is resistant to all concen-
trations at temperatures up to boiling.
Esters From the corrosion standpoint, esters are compar-
able with organic acids.
Fatty acids Up to about 300 F (150 C), Type 304 is resistant to
fats and fatty acids, but Type 316 is needed at 300
to 500 F (150 to 260 C) and Type 317 at higher
temperatures.
Paint vehicles Type 316 may be needed if exact color and lack of
contamination are important.
Phthalic anhydride Type 316 is usually used for reactors, fractionating
columns, traps, baffles, caps and piping.
Soaps Type 304 is used for parts such as spray towers, but
Type 316 may be preferred for spray nozzles and
flake-drying belts to minimize offcolor product.
Synthetic
detergents
Type 316 is used for preheat, piping, pumps and
reactors in catalytic hydrogenation of fatty acids to
give salts of sulfonated high molecular alcohols.
Tall oil (pulp and
paper industry)
Type 304 has only limited usage in tall-oil distilla-
tion service. High-rosin-acid streams can be han-
dled by Type 316L with a minimum molybdenum con
tent of 2.75%. Type 316 can also be used in the
more corrosive high-fatty-acid streams at tempera-
tures up to 475 (245 C), but Type 317 will probably
be required at higher temperatures.
Tar Tar distillation equipment is almost all Type 316
because coal tar has a high chloride content; Type
304 does not have adequate resistance to pitting.
Urea Type 316L is generally required.
Pharma-
ceuticals
Type 316 is usually selected for all parts in contact
with the product because of its inherent corrosion
resistance and greater assurance of product purity.

9
These comments on the suitability of stainless steels in various
environments are based on successful applications and are intended
as starting points for material selection for heat exchangers. In certain
media, for example, corrosion rates can be sharply affected by small
differences in temperature and chemical content, such as might occur
during upsets in the process. The magnitude of the possible effect can
be considerable, as indicated in Figures 2 and 3. Figure 2 shows how
small quantities of hydrofluoric and sulfuric acids can have a serious
effect on Type 316 stainless in an environment of 25% phosphoric
acid,
5
and Figure 3 shows how temperature affects corrosion rates of
type 304 and 316 in very concentrated sulfuric acid.
4

In general, as temperature increases the corrosion rate also in-
creases. A rule of thumb is that the corrosion rate of a material
doubles for each 30C rise in temperature. Also, major differences in
temperatures of heat exchanger surfaces can cause accelerated
attack, as suggested by the data in Table 3. Heat exchange through a
tube or vessel wall usually results in greater attack to a metal than by
simply immersing the metal in a hot solution.
4

Each material selection problem must be solved on its own
merits. Selection must be based on knowledge of the problem, the
properties of the materials under consideration, and common sense.
Service tests are the most reliable way to determine the optimum
material of construction, especially under conditions of heat transfer.
ASTM G-4-68 (1974) is a recommended practice for carrying out such
tests.
The tests should cover corrosive conditions during shutdowns as
well as during operation. For instance, sulfuric, sulfurous and poly-
thionic acid condensates formed during shutdowns may be more cor-

Figure 3
Source: Climax Molybdenum Company
93% H
2
S0
4
with velocity of 0.1 foot/second
Small quantities of hydrofluoric and sulfuric acids can have
a serious effect on Type 316 stainless in 25% P
2
0
5

phosphoric acid with 1.5% F as H
2
SiF
6
at 190 F (90 C).

Figure 2
Source: Parker & Briggs
5

10
TABLE 3
Effect of Heat-Transfer Conditions on Corrosion of Stainless Steel
4

Control Tests
Without Heat Transfer
Corrosion Rate in mils/year
With Heat Transfer and
Specimen at Indicated Temperature

Acid
%
Concentration*

Type
Specimen
Temperature
F C
Corrosion
Rate
mils/year
230
110
257
125
284 F
140 C
Acetic 10
304L
316
214
214
101
101
<1
<1
<1
<1
<1
<1
<1
<1
50
304L
316
216
216
102
102
130
<1
210
<1
220
<1
250
<1
99.6
304L
316
244
244
118
118
69
<1
260
<1
340
13
20
10
Formic 10
304L
316
214
214
101
101
742
10
>1000
16
570
62
570
73
50
304L
316
217
217
103
103
>1000
39
>1000
58
>1000
60
>1000
84
88/90
304L
316
217
217
103
103
716
10
540
48
500
40
520
48
Phosphoric 10
304L
316
214
214
101
101
<1
<1
<1
10
2
13
4
9
50
304L
316
230
230
110
110
8
6
13
39
3
4
>1000
22
86
304L
316
208
230
97
110
>1000
9
22
110
>1000
215
>1000
35

* By weight
11
rosive than is the process stream during operation. Tests should also
be conducted under the worst operating conditions anticipated. Even
after a plant is on stream. it is helpful to have a continuous corrosion
monitoring program to determine the proper selection of the materials
and to evaluate equipment modifications and inhibitors. While
inhibitors are not commonly required in stainless steel systems, there
are conditions where they can perform a useful service. For example,
the general attack on stainless steel caused by contaminants in acetic
acid can, under some conditions, be controlled by the addition of oxi-
dizing agents, such as permanganate, dichromate, cupric and ferric
salts, or by air injection.
5

Cooling Water Conditions
While it is difficult to classify the chemical environments to which
a heat exchanger may be exposed, evaluation of cooling water (if the
exchanger is used for cooling or condensing) is relatively simple. Al-
though water varies widely from location to location, tests can be con-
ducted to determine its quality and corrosiveness, and materials can be
selected accordingly. Some general observations on different cooling
water types are worthy of comment.
Cooling towers. The use of spray ponds and cooling towers, which
is becoming increasingly popular because of water shortages and ther-
mal pollution problems, complicates the cooling water problem because
the tendency of these devices is to concentrate impurities such as sul-
fides and chlorides. Cooling tower applications have been highly suc-
cessful for both Types 304 and 316 stainless steel, especially in the
Southwest where ground water supplies are scarce, and in some cases
with the use of sewage effluent for makeup water.
Fresh water. In fresh water as found in virtually all inland locations
in the United States, it can be said that clean stainless steel heat ex-
change surfaces resist all forms of corrosive attack by fresh waters.
Exceptions have been reported, but investigation revealed that prob-
lems were related to dirty surfaces and could have been prevented.
Spotty conditions of fouling and scale can result in localized corrosion
of the lower alloyed stainless steels. It has been observed in power
plant condensers that fouling occurs in two ways: as a solid continu-
ous coating on the surface, or as small isolated or localized spots. Con-
ditions underneath continuous fouling are generally uniform and not
considered serious to stainless steel in fresh water, whereas spotting or
localized fouling can create concentration cells that are potential sites
for localized corrosion.
Polluted fresh water. Stainless steels offer special advantages in
handling so-called fresh water contaminated by acid, such as resulting
from acid mine drainage in the Monongahela River near Pittsburgh,
Pennsylvania. Tests conducted by utilities in these waters, which have
a pH as low as 3 and contain ferric ions, show that Type 304 stainless
steel is completely satisfactory.
Clean salt water. Type 316 stainless steel has been used success-
fully in sea water for heat exchange service, but only when great care
has been taken to keep the metal surfaces clean and free of fouling
deposits. It would be better to consider the higher alloyed stainless
steels, many of which have proven performance.
Polluted salt water. Here too, Type 316 and especially the higher
alloyed stainless steels, have been used. Metal surfaces should be
cleaned regularly to eliminate spotty deposits and to improve heat
transfer performance.
12
Contamination
Corrosion rate is not always the key factor in material selection.
The presence of minute amounts of metal in solution may be deleteri-
ous to product quality in certain instances, even when the corrosion
rate is low. A common example is in the production of pharmaceuticals,
where Type 316 is generally chosen because of its excellent corrosion
resistance. Even small amounts of metallic ions might affect product
quality, effectiveness or color. Another example is the selection of a
special grade of Type 304rather than Type 316for the production
of hydrazine by an improved Raschig process with chloramine as an
intermediate. Even tiny amounts of molybdenum catalyze the decom-
position of hydrazine. Freedom from contamination is one of the chief
reasons why stainless steels are preferred for heat exchangers in nu-
clear power plants, such as the feedwater heater bundle shown in
Figure 4.

Figure 4
Versatility of Stainless Steels
for Corrosive Environments
The versatility of stainless steels for heat exchangers is exempli-
fied by the wide range of alloys available to solve various corrosion
problems. For instance, Type 304 is the most widely used stainless
steel, but in some aggressive heat exchange environments it may suffer
crevice attack, pitting, or stress-corrosion cracking, such as in condens-
ers and coolers using brackish or sea water, or in processes having
fairly high chloride contents. When these problems occur, there are
other stainless steels more suitable for such environments, and which
will eliminate the specific corrosion problem. Consider the following:
Pitting or Crevice Corrosion If pitting or crevice corrosion are
due to chlorides, a stainless steel, such as Type 316 or 317 containing
2-3% and 3-4% molybdenum, respectively, is often suitable. For more
severe salt water conditions, it may be necessary to consider even
higher alloyed candidates from among the following proprietary aus-
tenitic stainless steels:
Alloy 6X (20Cr-23Ni-6Mo)
6

Alloy 216 (19.75Cr-6Ni-8.25Mn-2.5Mo-0.37N)
7

Nitronic 50 (22Cr-13Ni-5Mn-2.25Mo)
8

Alloy 20Cb-3 (20Cr-33Ni-2.5Mo-3.5Cu)
9

13
Alloy 6X, which is undergoing commercial development, has exhibited
excellent resistance to pitting and crevice corrosion in salt water en-
vironments, such as in power plant condensers.
All four proprietary alloys mentioned above plus Type 317 per-
formed well in heat exchangers in desalination tests that were con-
ducted over a three-year period in Freeport, Texas.
10
In these tests,
deaerated sea water heated to 250F (121C) in a 3000-gallon-per-day
desalination test plant was evaporated to produce fresh water.

Stress-Corrosion Cracking The austenitic stainless steels may
be subject to stress-corrosion cracking in chloride environments at
high temperatureabove approximately 130-140F (54-60C)if tensile
stresses are present.
The mechanism of stress-corrosion cracking is not fully under-
stood, but there are methods to minimize the hazardparticularly
through material selection. For instance, AISI Type 329 is an austenitic/
ferritic stainless steel (25-30% chromium, 3-6% nickel, 1-2% molyb-
denum) that exhibits superior resistance to chloride stress-corrosion
cracking; plus it has a general corrosion and pitting resistance similar
to Type 316. Recent studies by Climax Molybdenum Company indicate
that Type 317 with 3.5% (minimum) molybdenum has excellent resist-
ance to stress-corrosion cracking. Such an alloy has been shown to
have excellent performance in a flue-gas desulfurization environment.
Proprietary Alloy 18-18-2 (18Cr-18Ni-2Si)
11
is another austenitic stain-
less steel that has been shown to be highly resistant to stress-corrosion
cracking in hot chloride environments, and it exhibits a general corro-
sion resistance at least equal to Type 304.
The ferritic stainless steels should also be considered when a
stress-corrosion cracking potential exists. The immunity of straight-
chromium, ferritic stainless steels to chloride stress-corrosion cracking,
such as Types 405, 410, and 430, has been known for many years.
12, 13

It has been demonstrated that the corrosion resistance of ferritic stain-
less steels can be improved by increased chromium and molybdenum
contents,
14, 15
and that their ductility, toughness and weldability can be
improved by reducing the carbon and nitrogen contents.
16
The recent
commercialization of new stainless steel melting and refining proc-
esses has made the purer ferritic stainless steels economically
attractive.
The specially melted and/or alloyed ferritic stainless steels of par-
ticular interest for heat exchanger service can be classified as follows:
those with about 18% chromium, which have corrosion resistance
qualities similar to that of Type 304, and those with more than 18%
chromium, which have resistance to corrosion comparable or superior
to that of Type 316. The ferritic stainless steels referred to are not
standard AISI grades; they are proprietary alloys.
Three of the proprietary ferritic stainless steels commercially
available are:
18Cr+titanium (Alloy 439)
17

18Cr-2Mo
18

26Cr-1Mo
19
(electron beam refined)
In various stages of commercial development are:
26Cr-1 Mo+titanium
20

29Cr-4Mo
21

29Cr-4Mo-2Ni

Commercial development means thatat this writingthe stain-
less steels mentioned are limited in availability and can be obtained on
special order. They are mentioned and should be considered as candi-
date materials for high-chloride applications, because they show up
14
TABLE 4
Mechanical Properties at
Elevated Temperature
Creep Strength ksi (MPa)
(Load for 1% Elongation
in 10,000 hr)

304 & 304L

309 & 309S

310 & 310S

316 &
316L

1000 F (538 C)
1100 F (593 C)
1200 F (649 C)
1300 F (104 C)
1500 F (816 C)
20 (137)
12 (83)
7.5 (52)
4 (28)
1.5 (10)
16.5 (114)
12.5 (86)
10 (69)
6 (41)
3 (21)
33 (228)
23 (159)
15 (103)
10 (69)
3 (21)
25 (172)
17.4 (120)
11.6 (80)
7.5 (52)
2.4 (17)

Scaling Temperature F (C)

Max. Continuous Service 1650 (899) 1950 (1666) 2050 (1121) 1650 (899)
Max. Intermittent Service 1550 (843) 1850 (1010) 1900 (1038) 1550 (843)

well in service and in standard laboratory tests for pitting and stress-
corrosion cracking. The high-chromium ferritic stainless steels have
resistance to chlorides previously obtainable only in the high-nickel
and titanium alloys.

Intergranular Corrosion Carbide precipitation occurs in some
stainless steels when heated and cooled, such as in welding. If
this occurs and the stainless steels are subsequently exposed to ag-
gressive environments, intergranular corrosion may occur in the zone
affected by the heat. Although this problem can be solved by heat
treating the final part, it is generally better to avoid the problem entirely
simply by selecting the right stainless steel.
When stainless steels are heated above 1000F (538C) and cooled
slowly, the chromium along grain boundaries tends to combine with
carbon to form chromium carbides. The resulting chromium-depleted
areas adjacent to the carbides have less resistance to corrosion, which
paves the way for intergranular attack. The less the carbon content of
the steel, or if an alloying element is present that preferentially com-
bines with the carbon (such as columbium, titanium, etc.), chromium
carbides do not form, and the grain boundary areas do not become
chromium depleted.
The low-carbon gradesTypes 3041L, 3161L, and 317Lare
recommended if weldments will be made and exposed to environments
in which intergranular attack is likely to be encountered. Likewise for
Types 309 or 310, which are selected for high-temperature heat ex-
change service, there are low-carbon variations, Types 309S and 310S,
respectively.
Type 321 stainless (17-19Cr, 9-12Ni) is stabilized against sensi-
tization to intergranular attack by the addition of titanium in proportion
to the carbon content, while Types 347 and 348 are stabilized with
columbium.
Among the above proprietary stainless steels, Nitronic 50
and Alloy 20Cb-3 are stabilized while Alloy 216 is available
with a low carbon content. The electron beam refined Alloy E-Brite 26-1
has an extremely low carbon content while titanium is used as a
stabilizer for Alloys 26Cr-1 Mo+titanium and 18Cr+titanium (Alloy 439).
Alloy 18Cr-2Mo is stabilized with either titanium or columbium, or with
a combination of both alloying elements.

HIGH-TEMPERATURE RESISTANCE
Selecting a stainless steel for high-temperature service is complex
because of the many factors involved. Mechanical and physical prop-
15

. 317

321

347 & 346

410

430

446

23 (159)
16.8 (116)
11.2 (77)
6.9 (48)
2.0 (14)
18 (124)
17 (117)
9 (62)
5 (34)
1.5(10)
32 (221)
23 (159)
16 (110)
10 (69)
2 (14)
11.5 (79)
4.3 (30)
2 (14)
1.5 (10)

8.5 (59)
4.7 (32)
2.6 (18)
1.4 (10)

6.4 (44)
2.9 (20)
1.4 (10)
0.6 (4)
0.4 (3)

1700 (927) 1650 (899) 1650 (899) 1300 (704) 1550 (843) 1950 (1666)
1600 (871) 1550 (843) 1550 (843) 1450 (788) 1650 (899) 2050 (1121)

erties as well as corrosion resistance must be considered.
For instance, specific interest in gas-metal reactions at elevated
temperatures has been generated by use of higher temperatures and
more corrosive fuels and by conditions associated with some of the
newer chemical processes. Most of the activity in this field has centred
around oxidation by air.
Of the three major components in stainless steels, chromium is
the most important in determining the degree of oxidation resistance
under constant temperature conditions (Figure 5). Table 4 gives both
scaling resistance and strength properties of those stainless steels
used for heat exchange service at elevated temperature.
As the high-temperature environment becomes contaminated by
the presence of various compounds of sulfur, carbon, hydrogen, and
the halogens, the problem of materials selection becomes even more
complex. Therefore, special care should be taken to assure selection
of the correct type of stainless steel. A fairly comprehensive discussion
of the application of the austenitic chromium-nickel stainless steels in
high-temperature environments is found in reference 22.
Figure 5
16

Figure 6
Paul Mueller Company
LOW-TEMPERATURE RESISTANCE
Of primary importance to the development of the world's natural
gas supplies is the storage and handling of liquid natural gas (LNG).
Heat exchangers have a role in LNG processing, such as the unit shown
in Figure 6, and in other cryogenic applications.
Austenitic stainless steels are the most widely used materials in
cryogenic applications, especially Type 304, because of their excellent
toughness and ductility. Not only does Type 304 remain tough at LNG
temperatures-minus 260F (162C), but it retains these properties
for use with liquid hydrogen (423F or 253C) and liquid helium at
452F (268C). Its thermal conductivity is also suitable for low-tem-
perature use. Table 5 shows low-temperature mechanical properties
of several stainless steels used in cryogenic service.
TABLE 5
Cryogenic Properties of Stainless Steel
AISI
Test
Temperature
Yield
0.2%
Strength
Offset
Tensile
Strength

Izod

Impact
TYPE F C ksi kg/mm
2
ksi kg/mm
2

%
Elongation
in 2"
(5.08 cm)
%
Reduction
of Area
ft-Ib kg-m
304 -40 -40 34.0 24.0 155.0 109.0 47.0 64.0 110 15.2
-80 -62 34.0 24.0 170.0 120.0 39.0 63.0 110 15.2
-320 -196 39.0 27.0 221.0 155.0 40.0 55.0 110 15.2
-423 -252 50.0 35.0 243.0 171.0 40.0 50.0 110 15.2
316 -40 -40 41.0 29.0 104.0 73.0 59.0 75.0 110 15.2
-80 -62 44.0 31.0 118.0 83.0 57.0 73.0 110 15.2
-320 -196 75.0 53.0 185.0 130.0 59.0 76.0 Not Available
-423 -252 84.0 59.0 210.0 148.0 52.0 60.0 Not Available
430 -40 -40 41.0 29.0 76.0 53.0 36.0 72.0 10 1.4
-80 -62 44.0 31.0 81.0 57.0 36.0 70.0 8 1.1
-320 -196 88.0 62.0 92.0 65.0 2.0 4.0 2 0.3
410 -40 -40 90.0 63.0 122.0 86.0 23.0 64.0 25 3.5
-80 -62 94.0 66.0 128.0 90.0 22.0 60.0 25 3.5
-320 -196 148.0 104.0 158.0 111.0 10.0 11.0 5 0.7
17
HEAT TRANSFER PROPERTIES
OF STAINLESS STEELS
The heat transfer properties of materials used in the construction
of heat exchangers cannot be based exclusively on the thermal conduc-
tivity of the metal itself. If this were the case, stainless steels would
lose out in most applications because published text book figures
place stainless steels in an unfavorable position in comparison with
other metals.
The power generation industry, however, after very carefully ana-
lyzing the heat transfer characteristics of heat exchanger materials, has
conclusively demonstrated that stainless steels are superior to
other metals when it comes to performance in actual service.
For instance, the curves in Figure 7 show the results of a two-year
test of overall heat transfer coefficient of two materials in identical heat
exchanger service. In the early stages, the relative performance of both
materials corresponded to values established by the Heat Exchange
Institute. However, in only 240 days, the overall heat transfer rate of
the stainless steel was found to surpass that of the Admiralty brass.
The heat transfer rate for both materials deteriorated with time, but that
of the Admiralty brass deteriorated more rapidly because of the action
of both fouling and corrosion, while the stainless steel was affected
only by fouling.
23

Figure 7
Source: McAllister
23

18
Similar results are suggested by Schrieber et al, as shown in Fig-
ures 8 and 9. Heat transfer rates of four tubing materials were com-
pared over a 70-day period at a desalination test facility in Texas. In
each case, the heat exchange performance of stainless steel showed
less degradation than the other three metals exposed to identical
conditions.

Figure 8
Source: Schrieber
24

Figure 9
Source: Schrieber
24

19
Steam Side Water Film 18%
Steam Side Fouling 8%
Tube Wall 2%
Water Side Fouling 33%
Water Side Film 39%

Figure 10
Figure 10 is a graphic representation illustrating the various
factors affecting resistance to heat transfer in actual service. It is
obvious that the films and scale that form on either side of the heat
transfer surface affect overall performance to a far greater degree than
the metal wall, which accounts for only 2% of the total resistance to
heat flow.
Film resistance is dependent on the type of fluid involved as well
as its velocity (Table 6). Scale resistance is related to corrosion of the
metal and the buildup of fouling deposits. Since corrosion is at a mini-
mum with stainless steel and it requires less cleaning, in practice there
would be less difference among the four metals than indicated. More-
over, the values in the table are based on equal thickness. On the
basis of equal strength, the stainless steel could be used in a thinner
wall, which in turn increases its overall heat transfer efficiency.
TABLE 6
Effect of Metal Conductivity on U Values
Application

Material

Film Coefficients
Btu/hr sq ft F
H
O
h
i

Thermal
Conductivity
of Metal
Btu/hr sq ft F/in.

Metal
Thickness
Inch

U
Value
Btu/hr sq ft F

Heating Water
with Saturated
Steam
Copper
Aluminum
Carbon Steel
Stainless Steel
300 1000
300 1000
300 1000
300 1000
2680
1570
460
105
0.0747
0.0747
0.0747
0.0747
229
228
223
198

Heating Air
with Saturated
Steam
Copper
Aluminum
Carbon Steel
Stainless Steel
5 1000
5 1000
5 1000
5 1000
2680
1570
460
105
0.0747
0.0747
0.0747
0.0747
4.98
4.97
4.97
4.96
where h
o
= outside fluid film heat-transfer coefficient
h
i
= inside fluid film heat-transfer coefficient
stainless steel is any grade in 300 series
Source: Tranter Mfg., Inc.
1 0
h
1
ty conductivi thermal
wall metal of thickness
h
1
1
U
+ +
=
20
CLEANLINESS OF STAINLESS STEELS
Two additional quailties of stainless steels that are important to
heat exchanger service are cleanability and freedom from fouling.
Most stainless steels in heat exchanger service resist chemical
and biological fouling. Because the metal often does not suffer general
corrosive attack, surfaces remain smooth and bright offering little op-
portunity for accumulation of fouling or deposits. If fouling should
occur, cleaning can be performed either chemically or mechanically.
For chemical cleaning, the best acids to use are citric, formic, or
sulfamic. These should be used under the supervision of qualified per-
sonnel. WARNING: Hydrochloric or inhibited hydrochloric acids should
not be used with stainless steels since this acid can be extremely
corrosive to all stainless steels.
A variety of mechanical means are also available for cleaning
tubular heat exchangers, including one or two continuous, in-service
processes. Extreme high-pressure water is also effective for cleaning
both inside and outside tubular surfaces and exterior surfaces of flat-
plate type exchangers.

DESIGN VERSATILITY
Stainless steels are available as sheet, strip, plate, bar, wire,
tubing, and pipe. This variety of product forms, the wide range of sizes

Figure 11
21
in which these forms are available, and the fabrication versatility of
stainless steels provide manufacturers with unlimited flexibility. Heat
exchanger manufacturers-specialists or job-shop fabricatorscan
produce equipment to meet most process requirements.
Shell-and-tube heat exchangers, for instance, shown by the
examples in Figures 11, 12, and 13 have long been the standard design
for most applications. These units use practically all of the mill forms
mentioned above. Tubing is the heat exchange surface. Plate is used for
tubesheets, heads, shells, and flanges. Bar is forged into fittings, such
as valve stems, while wire is formed into fasteners. Pipe is used for
connections, and sheet is used for baffles and tube supports. The unit
in Figure 13, for example, is Type 316L stainless steel throughout.
Figure 13
Struthers Wells Corporation
Figure 12
Fluor Corporation
22

While most designers are acquainted with the conventional type of
shell-and-tube heat exchanger, there are lesser-known types that offer
advantages in some applications, with respect to versatility, efficiency,
or compactness. For instance, many heat exchange surfaces are fabri-
cated from two sheets welded to form a series of passes through which
a heating or cooling medium flows. Platecoil and Temp-Plate are
two trade names for these plate-type exchangers. The plates can either
be embossed prior to fabrication as shown in Figure 14, or the assem-
bled plate exchanger can be expanded by pressure after fabrication,
such as the design in Figure 15.
Figure 14
Brighton Corporation, Tranter Mfg. Inc., Texas Instruments
Figure 15

23
The most frequent use of the flat heat transfer surfaces is for
immersion in tanks for the heating or cooling of solutions, such as in
Figures 16 and 17, or as evaporator surfaces where liquids cascade
down the outside.
In many applications, however, the transfer surface is integral
with the vessel itself, actually being the vessel wall, such as the
jacketed vessels shown in Figures 18 and 19.

Figure 16
Tranter Mfg. Inc.
Figure 18
Figure 17
Figure 19
Panhandle Manufacturing, Inc.
Subsidiary of Tranter Mfg. Inc.
24
Plate-type exchangers are also constructed of alternating layers of
thin plates and corrugated sections, such as the one shown in Figure
20. They are similar in appearance to plate-and-frame filters. Integral
channel and manifold sections enclose the open ends. The process
material flows into the corrugated openings.
Plate exchangers give better heat-transfer efficiencies than shell-
and-tube units; also the plate type has a lower pressure drop at the
same heat transfer coefficient. In Figure 21, a plate heat exchanger
does double duty, cooling condensate from a pulp mill digester and heat-
ing incoming process water. The digester blow-down is collected and
condensed to eliminate one source of malodorous compounds in a pulp
mill while the heat is reclaimed for energy conservation. Figure 22
shows a plate heat exchanger used in steel mill operations.
Spiral heat exchangers in essence consist of one spiral wrapped
around another, as illustrated in Figure 23, so the same flow character-
istics are obtained for each medium. Its advantages include compact
design, ability to handle sludges and slurries with low fouling incidence,
and adaptability for liquid-to-liquid or liquid-to-vapour service. Figure 24
shows two spiral exchangers, one vertical and the other horizontal. The
vertical unit cools phenol while the horizontal unit cools condensate for
two gas atmosphere generators. Both are constructed of Type 316
stainless steel.

Figure 21
American Heat Reclaiming Corporation
Figure 22
Figure 20
25
Figure 23

Figure 24
26
To increase the heat transfer performance of an exchanger using
tubing, the surfaces of stainless steel tubing can be enhanced.
Tubing can be spirally indented or double fluted, which tends to alter
the flow characteristics around the tube surface both inside and out
(Figure 25). Integral-finned tubing is available in which fins are formed
circumferencially on the outside surface (Figure 26), increasing the
external surface area about 2.5 times. Fins can also be attached to
stainless tubing to increase surface area, especially useful for air
coolers. Bi-metallic tubing is also available to provide answers to dual
corrosion or erosion problems that cannot be solved by one material
alone (Figure 27).
Tube-in-tube exchangers are also used, such as in food processing
and sewage treatment. One such unit is shown in Figure 28.

Figure 26
Integral-Finned tubing offers 2.5 times the external surface area of equivalent-diameter, bare-
surface tubing. It is manufactured to ASTM A-498 from 0.500" OD to 1.000" OD, in wall thick-
nesses ranging from 0.049" (18 BWG) to 0.083" (14 BWG), and in lengths up to 50 feet.
Figure 25
For improved heat transfer, stainless steel tubing can be
enhanced by commercially available techniquessuch as
spiral indentation or double fluting. In one falling-film
evaporator test comparing fluted- and nonfluted stainess
steel tubes, the heat transfer of the fluted tube was about
45 percent better. A small section of double-fluted stainless
is shown.
Figure 27
Bi-Metallic tubing is the single answer to dual corrosion and
erosion problems in condensers. It is available as fully
finished stainless tubing mechanically bonded to the entire
ID or OD surface of either carbon, brass, copper, stainless,
or other alloy tubing.

Type 304
stainless tube sheet
Type 304 welded
stainless tube inside,
to handle corrosive
process gas
Ferrule ofType304
stainless for rolling
into tube sheet
Deoxidized copper tube
outside to handle corrosion
from cooling water
Inlet process temperature
on tube side above 150C.
Inlet cooling water
on shell side 40C.
27
Figure 28
STAINLESS STEELS ARE ECONOMICAL
The following outline can help in evaluating the economics of
candidate materials for heat exchange service. A cardinal rule is that no
material should be eliminated from consideration on the basis of its
initial purchase price alone.
1. List all materials suitable for the process.
2. For each material, list sizes and quantities based on corrosion
resistance, oxidation resistance, strength, and heat transfer.
3. Estimate total cost for each material, including fabrication costs,
capitalized costs, etc.
4. Is intended unit life a factor; will the process be phased out after
a given number of years? If so, a material that corresponds to
this unit life should be given strong consideration.
6. Calculate replacement and maintenance costs for each material,
including costly production losses due to shutdowns.
7. Compile and compare costs.
8. Eliminate all but the most economical materials.
9. Work the remaining materials through the process unit design
with a complete economic evaluation.
10. Pick the material that yields the best return on investment.
At the design level, consult a stainless steel supplier. A list of the
companies represented on the Committee of Stainless Steel Producers
appears on the back cover of this publication.
28
COMMENTS ON
INSTALLATION AND MAINTENANCE
Tube-rolling practices and tolerances recommended by the Tubular
Exchanger Manufacturers Association (TEMA) should be followed, to
avoid problems of over-rolling, such as described in the example on
food processing (Page 32). In that application, the tubesheet hole sizes
were as much as.035" (0.889mm) above the nominal tube size. For a
2"-diameter (50.8mm) tube, TEMA recommends a hole diameter of
2.018" (+ .003" or - .007") (51.26mm). In the food processing example,
the tubesheet hole oversize was twice what it should have been.
When any shell-and-tube heat exchanger is to be retubed, the
holes in the tubesheets should be carefully measured and the sizes
transmitted to potential tube suppliers in order to obtain tubes of
optimum size, remembering, of course, that tubing is manufactured
to ASTM specifications.
Protrusion of tubes above the top tubesheet of a vertical exchanger
should be avoided. If tubes are too long and a protrusion results, it
should be applied to the bottom tubesheet. This measure will help
eliminate areas where chlorides or other aggressive elements can be
trapped and concentrated, and it will facilitate draining when the unit is
shut down.
The area beneath the top tubesheet of vertical heat exchangers is
another potential trouble spot, as illustrated by the two drawings in
Figure 29. If a process liquid or cooling water is on the shell side and
the heat source on the tube side, this area has potential for higher
temperatures or alternate wetting and drying-both of which can
increase the potential for corrosion. (Stress-corrosion cracking of
austenitic stainless steels is common under these conditions.) The
lower drawing shows how to properly port this area to prevent such
problems.
The time during which a heat exchanger is down, in many in-
stances, may be more critical in terms of corrosion than when the unit
is in operation. If the process stream is allowed to remain without
motion in contact with heater tubes, temperatures can increase, aggres-
sive solutions can concentrate, and corrosive conditions can become
more severe. Prompt draining and flushing followed by thorough drying
should be standard operating procedure for shutting down any heat
exchanger.
There are, of course, situations in which the above practices
cannot be applied. One example is in reheater exchangers following
wet scrubbers in coal-fired power plants. During an outage, it may be
desirable to keep steam flowing through reheater tubes in order to keep
temperatures on tube surfaces above the dewpoint of various constitu-
ents in the flue gas. In SO
2
scrubbers, condensing sulfurous or sulfuric
acids can lead to early failure of reheater tubes (Figure 30).
Removing scale from heat exchanger surfaces often necessitates
the use of acids. As previously stated, hydrochloric acid (inhibited or
not) should not be used. With any acid, care should be exercised and
it's always advisable to consult with the metallurgist or corrosion
engineer. For example, Type 304 stainless steel tubing may be ideal for
a certain process. However, if acid cleaning is used, tubing that has
been welded to the tube sheet may suffer localized attack in the weld
area.
Since the corrosive effect of any acid is dependent on the tempera-
ture, be sure both acid and tubes are cool. If it is necessary to use hot
acid cleaning, heat the acid prior to pumping into the heat exchanger
so the metal surface will be the same temperature. If steam is used to
heat the acid in the exchanger, the metal temperature is approximately
that of the high temperature steam and the corrosion rate can be very
high. Figure 30a
Kansas City Power & Light Company
29
Vapour Trapped in
Vertical Heat Exchanger
Trapped Vapour
Area of increased corrosion
because of alternate wet-dry
conditions.
Heat Exchanger
Vessel Shell
Vapour Released in
Vertical Heat Exchanger
Vapour Bleed
Heat Exchanger
Vessel Shell
Figure 29

BAD
Tubesheet
Flow In
Tubes
CORRECT

Tubesheet

Flow In
Tubes
Figure 30b
30

Figure 31
PULP AND PAPER
In the Kraft process a solution of sodium sulfide in caustic soda
digests the wood binder, lignin, yielding a fibrous pulp that is converted
into coarse Kraft or very fine white papers. Following digestion of the
lignin, the cooking chemicals (referred to as black liquor) are washed
out of the pulp, concentrated, and burned in a recovery furnace. The
organic material burns away leaving molten sodium carbonate and
sodium sulfide, which after slaking with water are recausticized with
lime and recycled to the pulp digester. The Kraft process is popular in
the United States because it can be used for pulping almost any wood
type, it yields fibers of comparatively high strength and chemical
recovery improves plant operating economics.
There are numerous heat exchanger applications in Kraft pulp
and paper mills for heating pulping chemicals, for concentrating black
liquor, for condensing odorous vapours in air pollution control systems,
and for recovering process heat. The design of these heat exchangers,
however, is as varied as their applications; including flat plate, spiral,
and the more conventional shell-and-tube types.
An important feature of the Kraft process is the recovery of heat
and pulping chemicals by burning black liquor in a furnace. However,
in order to support combustion, the liquor must first be concentrated to
about 65% solids, usually in a series of five or six vertical-tube evap-
orators (Figures 31, 32, and 33). In a multiple effect unit, it is common
practice to tube the entire series of evaporators with stainless steel,
Figure 32
Ecodyne Unitech Division
Typical six-effect evaporator with concentrator
Multiple Effect Evaporators

31
either Type 304 or 316 depending upon conditions. Stainless steels
were originally used only in the first two and last two evaporators to
help reduce problems with scale. However, mills are increasing their
efforts to contain pollution discharges. Strong wastes from spills are
being piped to evaporators, consequently exposing them to more severe
corrosive conditions. Now, even the shells and vapour chambers are
being fabricated of Type 304 or 316.
One of the principal reasons for using stainless steels in pulp and
paper mill heat exchangers is to prevent iron contamination or dis-
coloration of chemical pulps, which are made into paper. Stainless
steels are also used for their resistance to oxidation at elevated temper-
ature, low sparking characteristics (especially important where turpen-
tine vapours, acetone, alcohol, and other hazardous vapours are
present), and light-weight design potential. Stainless steel pipe runs and
heat exchangers at various plant elevations require less supporting
structure.
Liquor heaters in both kraft and sulfite mills are another significant
f i l l h h

Figure 33
32
FOOD PROCESSING
Condensers and other heat exchanger systems are often the most
critical components in food processing lines. It is here that heat con-
centration is most intense and where thin-walled tubing is most vulner-
able to corrosive elements. Welded stainless steel tubing is saving
many food processing plants from interrupted production and costly
repairs because of its ability to resist corrosive damage.
For example, conventional materials for heat exchanger tubing in
cane and beet sugar refineries used to be carbon steel and copper-base
alloys. The copper alloys, however, were subject to cracking by the
ammonia present in sugar solutions. This problem was aggravated by
increased use of ammonium phosphate fertilizers.
To eliminate the problem, sugar refineries switched to economical,
thin-wall stainless steel tubing, specifically Types 304 and 316, which
resist attack by ammonia or carbon dioxide. In addition to excellent
corrosion resistance, these austenitic stainless steel tubes resist abra-
sion from silt-like subtances in sugar solution by-products. They also
resist scale build-up. (Figure 34)
Although stainless has a heat conductivity only 1/7 that of brass
and 1/3 of carbon steel, experience demonstrated that scale buildup in
sugar heat exchanger tube surfaces is more important than the thermal
conductivity of the metal itself. Stainless tends to reduce the adherence
of such deposits.
Stainless steels are not immune to corrosion, however, and while
problems are few in sugar refining, proper installation and cleaning
techniques are necessary if corrosion is to be avoided.
For example, it was reported
25
that one refinery experienced stress-
corrosion cracking in the third unit of a five-effect, vertical tube
evaporator system. The unit contained 750 Type 316 stainless tubes,
2" OD x 0.063" wall thickness X 20' long (50.8 x 1.6 X 6096 mm).
Eighty of the tubes cracked after only two years of service.
Laboratory examination confirmed the failed tubes to be annealed
Type 316 stainless. Inspection of the evaporators, however, revealed
the following probable causes:
1. The holes in the tube sheet were as much as .035" (0.889 mm)
over the nominal tube dimension.
2. Approximately .5" (12.7 mm) of each tube protruded above the
upper tubesheet.
3. The tubes were cleaned with hydrochloric acid without adequate
neutralizing or flushing after cleaning.
4. During standby, steam continued on the shell side with nothing
but air on the tube side.
Conditions for chloride stress-corrosion cracking were present. The
weirs created by the tubes protruding above the tubesheet provided an
ideal situation for the entrapment of chloride ions; the temperature was
sufficiently high to concentrate the chlorides; oxygen was present; and
the stresses resulting from over-rolling were above acceptable limits.
In another beet sugar processing plant, a heater is used for pre-
heating reconstituted nonsugar products prior to evaporation. Sulfuric
acid is added to the process and temperatures reach 200F (93C). To
minimize the chances of stress-corrosion cracking and pitting in this
low-pH environment (containing chlorides), the plant is using Type 329
stainless steel tubing, which provides better resistance to corrosion and
somewhat higher strengths than Type 304.
In a soybean processing plant, nonferrous tubing in a solvent
extraction system was suffering corrosion from steam, hexane vapours,
and amino acids. The brunt of the corrosive attack was absorbed by two
condensers-a pre-evaporator unit and a desolventizer-toaster
condenser. The two units contained 1247 tubes " OD x 10' (19.05
3048 mm). Cooling water is circulated on the tube side at 22 psi
Figure 34
33
(152 MPa), 60-100F (16-38C). Hexane, steam, and amino acids at 200F
(93C) circulate on the shell side. The first set of tubes was phosphorized
Admiralty tubing. This set failed in two years from stress-corrosion, fatigue
cracking, and pitting and was replaced by 18-15 red brass, which failed by
fatigue in two years. The final installation, which is still in service after
several years, was made with Type 304 stainless steel.
Innovation is a part of the food processing industry, and fairly recent
is the use of heat exchangers for continuous processing of foods instead
of the steam kettle batch process. Continuous processing utilizes a
scraped surface exchanger, such as shown in Figure 35; and stainless is
preferred when high-temperature and low pH are involved.
Figure 35
Votator Division, Chemetron Corporation
A typical application is process and hot pack of spaghetti sauce
with meat or mushrooms. The food has a pH of less than 4.2, and it
requires heating to 250-260F (121-127C). After holding at temperature
for a specified period to effect complete sterilization, hot filling is
accomplished at 200-205F (93-96C). This system uses Type 316 through-
out. Similar applications are encountered in salad dressing processing
and in edible oils, which contain high percentages of free fatty acids.
NITRIC ACID PRODUCTION
Nitric acid is produced by the oxidation of ammonia to nitric oxide
over a platinum-rhodium catalyst, subsequent oxidation to nitrogen
dioxide, and finally reaction with water. The process operates under a
pressure of up to 8 to 10 atmospheres. The chemical reactions are
as follows:
1. 4 NH
3
+ 5 O
2
4 NO + 6 H
2
0 + 216,000 k. cal.
2. 2 NO + O
2
2 NO
2

3. 3 NO
2
+H
2
O 2 HNO
3
+NO
In the overall process liquid ammonia is vapourized, heated, mixed
with compressed air, and passed over the platinum-rhodium catalyst in a
burner, or converter. Because the reaction is exothermic, the reacted
gases reach a temperature of up to 1760F (960C). To recover energy,
34

Figure 36
and to cool the gases for water absorption, they are passed through
a series of heat exchangers, referred to as the exchanger train.
(See Figure 36.)
Steam generated in the exchanger train is used to drive the air
compressor via a steam turbine. The acid gases leaving the exchanger
train pass through a nitric acid cooler, and a weak acid condenser
(also referred to as a cooler condenser), where the acid which con-
denses is at about 40% concentration. Both the cooled gas and the
condensed acid then pass to the absorption column, or absorber, where
they are absorbed in water entering the top. Concentrated nitric acid
from 58 to 65% concentration leaves the bottom, the concentration
depending upon absorber efficiency.
The stripped gas leaving the top of the absorber, called the tail
gas, is essentially nitrogen, but contains small amounts of nitrogen
oxides. Before it is discharged to atmosphere it is heated through the
series of heaters (items 7, 8, 3, and 2 in Figure 36) and passes through
a catalytic combuster and then the gas turbine.
Stainless steel tubing is used in most of the heat exchangers in this
train, as indicated in the sketch, as well as on the trays of the absorp-
tion column, for water cooling in the absorption process. (Figure 37)
Type 304L is frequently a suitable choice for the tubing in these
heat exchangers, although some plants indicate a preference for Type
329 in exchangers 3, 5, 6, and 8, and Type 405 in exchanger 3. Because
of the high gas temperature in the turbine-gas heater, Type 347 or 321
is generally used for this heater. In some cases Type 310 stainless has
been employed.
For the water cooled exchangers, such as items 5 and 6, chlorides
in the cooling waters at some plants may lead to chloride stress-
corrosion cracking from the cooling water side. For such units some
plants have upgraded to stainless steels that have greater resistance to
stress-corrosion cracking. (See discussion of stress-corrosion cracking
on page 13.)
For the absorber vessel and its trays and bubble caps, Type 304L
is the normal choice. As heat is generated in the absorption process,
* 6. Weak Acid Condenser- 304LTubes and Shell
7. Bleach Air Cooler-304LTubes- Steel Shell
8. Tail Gas Preheater-304LTubes- Steel Shell
9. Absorber Column Cooling Coils-304L and 430 Tubes
*Water Cooled
Nitric Acid Process
HEAT EXCHANGERS
1.Ammonia Vaporizer- SS Tubes- Steel Shell
2. Turbine Gas Heater-321 /347 Tubes and Shell
3. Tail Gas Heater- 304LTubes and Shell
4. Boiler Feedwater Heater -304 L Tubes and Shell
* 5. Nitric Acid Cooler- 304LTubes and Shell
35
Figure 37
Tranter Mfg. Inc.
water cooling through tubing coils (Types 430 or 304L tubing) on many
of the trays is employed.
Typical temperatures through the exchanger train are as follows:
1. Air Inlet500F (260C) (While not shown in the diagram, the air
from the compressor may pass through a heat exchanger just
ahead of the tail gas heater.)
2. In the catalyst bed of the burner (or converter)1760F (960C).
3. Inlet to the tail gas heater608F (320C).
4. Inlet to the nitric acid cooler428F (220C).
5. Outlet of the weak acid cooler104F (40C).

HIGH-TEMPERATURE RECUPERATORS
Heat exchange recuperators constructed of stainless steel sheet or
tubing recover useful process heat from hot gases that would otherwise
be lost to the atmosphere. This is of particular interest not only from the
fuel saving standpoint, but also in terms of helping with pollution con-
trol. For example, the steel and glass industries use recuperators to
cool exhaust gases to a point where they may be filtered through fabric
bags. In this manner, most of the particulate matter can be
economically removed.
Temperatures of exhaust gases from steel and glass plants usually
range up to 2400F (1315C), even as high as 2800F (1540C) in some
cases. Present recuperator designs are highly efficient and utilize a
variety of wrought and cast stainless steels. Alloys are selected for
durability of up to 10 yearsconsidering temperature and the corrosive
nature of the hot gases.
There are standard recuperator designs, such as shown in Figures
38, 39, and 40, but most installations are engineered on an individual
basis. The most common stainless steels used are Types 309 or 310 for
the high temperature applications and Type 304 for temperatures of
1200F (650C) and below. In some applications, straight-chromium
stainless steels have been used, such as Types 430 and 446 or Alloy
E-Brite 26-1.
36
Double-shell radiation recuperator with convection bundle.
Double-shell radiation recuperator ready for shipment.
Figure 38
The American Schack Company, Inc.
37

Flue-gas-thru-tube recuperator.
Figure 39
Figure 40
Flue-gas-thru-tube recuperator under assembly.
38
STATOR COOLING
Removing heat in a steam turbine generator by piping cold gas
through the insulation of current-carrying conductors was developed
and applied in the early 1950's. Early units used hydrogen gas in these
stator heat exchangers because of its superior heat characteristics
and low friction. Type 304 tubing was used because it is a nonmagnetic
material and will not heat up in an extremely strong alternating current
magnetic field. Not only does it reduce eddy current loss, but its good
strength permits thin-wall tubingallowing more room for copper in the
stator coil and maximum gas space inside the tubes.
Fusion research, which may be applied to electrical generation in
the 21st century, more than likely will use Type 304 for similar purposes.
According to current fusion research activity, Type 304 tubing and
cryogenic gases are used to supercool electrical conductors. By cir-
culating liquid hydrogen or nitrogen around electrical conductors they
are supercooled to cryogenic temperatures, at which point electrical
resistance is virtually nil. Type 304 prevents eddy current loss and it
has excellent properties at cryogenic temperatures.
Sulfuric Acid Manufacture
(Simplified Flow Diagram for Sulfur Burning Plant)
Note: Actually SO
3
is absorbed in H
2
SO
4
to make a stronger H
2
SO,
Figure 41
SULFURIC ACID
The standard grades of stainless steels are seldom used in sulfuric
acid solutions because of their narrow range of usefulness. According
to widely published data, Type 316 gives useful service at room tem-
perature in concentrations lower than 20% and higher than 80%.
Between 20 and 80% and at elevated temperatures the corrosion rate
of Type 316 increases rapidly, which severely limits its application in
heat exchangers*-except for the recent development of anodic
protection of Type 316 sulfuric acid coolers.
Manufacturing sulfuric acid involves both drying of sulfur dioxide
and absorbing of sulfur trioxide in concentrated acid (Figure 41). These
processes generate heat and require cooling of both the drying and
the absorbing acids.
Traditionally this cooling has been accomplished in coolers made
of cast iron, in which the concentrated acid flows inside the coolers,
and the cooling water cascades over tiers of pipes. Problems with these
39
coolers are rather frequent resulting in high maintenance costs, acid
losses, and pollution. The coolers also require considerable space.
* Note: Because of the narrow range of the standard stainless steels, it is fre-
quently necessary to upgrade to higher alloyed materials, such as Alloy 20Cb-3.
In the late 1960s, a Canadian company
26
introduced Type 316L
stainless steel coolers with an effective anodic protection system. These
coolers have performed well in almost six years of service and have
resulted in substantial savings due to: 50% saving in space, elimination
of ground pollution due to acid leakages, a sharp reduction in
maintenance, higher heat transfer efficiency, a high purity product with
an iron content of less than 5 parts per million, higher operating
temperature, and higher acid velocities without suffering erosion/
corrosion effects.
The anodic protective system for sulfuric acid coolers has also been
developed for air coolers for areas in which cooling waters are not
readily available. Temperatures for 90% sulfuric are 230F (110C) for a
shell and tube exchanger and 115F (46C) for air coolers. If the anodic
protection should be turned off or removed, the system would last for at
least six months.
An interesting sidelight is the fact that over 350,000 tube-to-
tubesheet joints have been made (by welding) for these sulfuric acid
coolers, and all have performed without failure.
PETROLEUM REFINING
Figure 42 is a flow diagram of a petroleum refinery showing typical
corrosive environments.
27
Specific data on high-temperature corrosivity
studies in this environment are contained in API Publication 943,
September 1974.
Stainless steels are used quite extensively in petroleum refining
heat exchangers for protection against corrosion by sulfur compounds
and various acids which may be present in the process. For instance,
Corrosives (underlined) Found in Refinery Operations
SOrganic Sulfur Compounds and H
2
S Above About 500F.
Figure 42
Source: Cooper
27

40
Figure 43 is a diagram
28
showing the relative resistance of carbon
steel, 5% chromium, 9% chromium steels and 18-8 stainless steels to
corrosion by crude containing 1.5% sulfur at a temperature range of
500-900F (260-482C).
The 400 Series stainless steels are not included in this diagram;
however, they would show a low corrosion rate, with Types 430 and 446
having about the same corrosion resistance as 18-8.
The diagram in Figure 43 demonstrates only one crude; other
crudes are more or less corrosive, which is a particularly difficult
problem many refineries must face with different crude sources. How-
ever, one point that should be noted is that the starting point of 500F
(260C) shows a very low corrosion rate. Usually 450F (232C) is the
starting point at which refineries will use stainless steels for sulfur
corrosion problems.
The following table gives some general rules as to where stainless
steels are used, based on operating temperatures in streams contain-
ing sulfur, hydrogen, and nitrogen.
Temperature Alloys
Above 700F (371C)

Types 304, 321, or 347. (Type 430 is subject
to 885F embrittlement at these tempera
tures.)
450-700F (232-371C) Types 430, 304, 321, or 347.
Below 550F (288C) Low alloy or carbon steels.
Below 250F (121C)

Type 430 may be used in some systems con
taining high hydrogen sulfide and ammonia.

Figure 43
Source: NACE98
Corrosion of Steels in Crude Oil
Containing 1.5% Sulfur
Another consideration for using stainless steels in petroleum refin-
ing heat exchangers is the presence of naphthenic acids. Naphthenic
acids are not too common throughout the world, although they are
prominent in California and Venezuelan crudes. The neut number (or
acid number) in some of these crudes is 1-2, with a few side streams
as high as 12. (Neut numbers of .5 and higher are considered corrosive.)
Naphthenic acids follow about the same corrosion pattern as the
sulfur compounds. However, it is theorized that these acids dissolve
iron sulfide scale that tends to be protective on the low alloy steels. So
as sulfur corrosion occurs at 450F-500F (232-260C), some naphthenic
acid corrosion can be expected in the same range.
Type 316 is the usual material to use with naphthenic acids, al-
though Type 304 has been used in streams with low neut numbers.
Above 5, and in the 650F-700F (343-371C) range, Type 316 with 2.75%
minimum molybdenum or Type 317 will offer better protection against
corrosion.
Heat exchangers are the most critical areas for naphthenic acid
corrosion because the acid has a narrow, 550F-700F (288-371C) boiling
range at which it tends to concentrate. Internal condensers and pump-
around coolers are typical areas in crude distillation where naphthenic
acid will be most severe.
In some refinery applications, the choice of material is predicated
on cooling water, which may contain chlorides, which can lead to
stress-corrosion cracking. In these cases, Type 329 or one of the higher
stainless steel alloys may be a better choice (Figure 44). Below 700F
(371C) the new ferritic stainless steels, such as Alloys 18Cr-2Mo and
26C r-1 Mo may be considered. (see page 13.)

Figure 44
41
Simplified Flow Diagram for Acetic Acid Process
(Aldehyde Oxidation)
Figure 45
Source: L. S. VanDelinder, P.E.
STAINLESS STEELS
IN ACETIC ACID
Heat exchangers used in a chemical unit producing acetic acid can
constitute the major equipment cost. These exchangers include
condensors, intercoolers, waste-heat boilers, calandrias and coolers,
the size and distribution depending on the process used. The simplest
(acetaldehyde) requires a minimum of 12 exchangers, as shown in
Fig. 45.
Although Type 304 stainless steel has utility in certain exchangers
operating at lower temperatures, the workhorse of the acetic acid in-
dustry is Type 316 (2-3% molybdenum) or its low-carbon counterpart
Type 316L. In some specific instances, Type 317 with a higher molyb-
denum content (3-4%) has better resistance to organic acids, such as
acetic acid. With Type 316, corrosion rates of less than 10 mils per year
should be experienced, as indicated by the data in Tables 7, 8 and 9.
TABLE 7
Field Corrosion Test for 82 Days in 99% Acetic Acid
Vapours at 212-250
0
F
29

MATERIAL: Indicated Corrosion Rate, Ipy
Type 304................................................ 0.066
Type 316................................................ 0.003

TABLE 8
Field Corrrosion Tests in Glacial Acetic Acid at
1250F. Vapour Velocity 175 ft/sec. Specimens
exposed in inlet leg of reaction coil.
29

Indicated Corrosion Rate, Ipy
MATERIAL:
Test A
450 Hours
Test B
1769 Hours
Test C
1384 Hours
Hastelloy C
Type 317 S.S.
Type 316 S.S.
Type 316 L
Illium
Alloyco 20
Type 309 S.S.
Hastelloy B
Hastelloy A
Inconel
Monel
Nickel
Type 410 S.S.
Type 430 S.S.
Type 446 S.S.
0.0001 (gain)
0.0004
0.0004
Not Tested
0.0002
Not Tested
Not Tested
0.0003
0.0033
0.13
Corroded Away
Corroded Away
Not Tested
Not Tested
Not Tested
0.0001
0.0004
0.0006
0.0006
Not Tested
0.0001
0.0004
0.0007
Not Tested
0.11
Not Tested
Not Tested
Not Tested
Not Tested
Not Tested
Not Tested
0.0012
0.0017
Not Tested
Not Tested
Not Tested
Not Tested
Not Tested
Not Tested
Not Tested
Not Tested
Not Tested
0.0015
0.0012
0.0002

42
TABLE 9
Corrosion Rates (in of Materials in 99.6% By mpy)
Wt Acetic Acid
30

Specimen Temperature, Degrees F

Without Heat
Transfer
With Heat Transfer
Material 230 244 230 257 284
Type 304L
Type 316
C.S. 20-Cb

69
<1
7
260
<1
5
340
13
2
20
10
100
Hastelloy B
Inconel
Monel
3
<1
22
1
7
36
120
7
45
68
3
14
220
Generalized isocorrosion curves are shown in Figures 46, 47 and
48. Such data do not provide accurate corrosion rates for a specific
application, but they allow a comparison of materials for economic anal-
yses or as a basis for further testing. Note that Type 430 stainless steel
has reasonably good resistance to acetic acid. However, the use of 400
Series stainless steels should be limited to emergency repairs. For the
small additional cost required, the use of Type 316 is warranted.
Steel shells may be used in these heat exchangers if the product
is on the tube side. Galvanic action between the mass of stainless steel
in the tube bundles and the steel shell is not excessive in most indus-
trial waters. Tie rods and baffles, however, are generally made of stain-
less to assure long life and to provide proper expansion characteristics
within the unit. Also, the design should consider the possibility of vibra-
tion that might develop, which results in the hammering of tubes with-
in the baffles.
Because most process waters contain chlorides, there is always
the possibility of stress-corrosion cracking of the 300 Series stain-
less steels. To minimize the possibility, it is good practice to vent the
tube sheet (in vertical exchangers) to prevent concentration of the chlo-
rides. Safe endingwelding short lengths of a stress-corrosion crack-

Figure 46
Figure 48
Figure 47
43
ing resistant stainless at the problem end of tubingwill also minimize
the problem. If a crack-resistant material is desired, consider the use of
Type 329 or the straight-chromium alloys described elsewhere in this
publication.
In some heat exchange applications in acetic acid plants, such as
esterification kettles in which the heating coil is internal, the use of
Type 316 may be borderline. The sulfuric or other acid catalyst added
to the acetic acid can produce excessive attack. However, Type 316
can be used with minimum corrosion simply by reducing the tempera-
ture slightly or adding oxidizing ions, such as cupric or ferric that tend
to ameliorate the corrosive attack.
Contaminants in acetic acid can increase corrosion rates. In some
processes the sulfur dioxide or sulfur trioxide present in the stream can
increase corrosion in an overhead condenser in which condensation
occurs at high temperatures. The addition of formic acid to acetic
acid will increase the rate of attack on stainless steels, although the
increase can be tolerated by Type 316.
Acetic anhydride in the acid stream will also increase corrosion
rates. When operating condensers, calandrias, or interchangers at acid
values higher than 100%, it may be necessary to use higher alloyed
material, such as Type 317, Alloy E-Brite 26-1, or Alloy 20Cb-3.
The presence of aldehydes, ketones, esters, and other organic
products in the acid stream does not increase corrosion rates; in fact,
their presence may even result in a decrease.
When consulting published corrosion data on candidate materials
for acetic acid heat exchangers, the temperature is a critical param-
eter. The anticipated wall temperature of the tubing on the process side
should be calculated and correlated to the test data. If this factor is an
unknown, the inlet temperature of the process stream must be used as
a basis for design.
At times, it's desirable to seal-weld tubes to tube sheets to fore-
stall intermixing of the two streams in a heat exchanger. When welding
is required, it is good practice to use Type 316L stainless to minimize
carbide precipitation in the weld zone.
STAINLESS STEELS
IN SYNTHETIC NATURAL GAS
In a double methanation, substitute natural gas plant, stainless
steels are used in heat recovery exchangers between the first and sec-
ond methanators.
In the high-pressure boiler, heat from the gas leaving the first
methanator is recovered by heating boiler feedwater. This gas is a mix-
ture of water vapour, carbon monoxide, carbon dioxide, hydrogen and
methane. The boiler feedwater cools the gas to a temperature below the
dew point of the water vapour. The condensed water forms a dilute
carbonic acid with carbon dioxide present. Low-alloy steels are subject
to a rapid erosion/corrosion failure in this atmosphere, consequently,
Type 304 stainless steel is used throughout.
In the low-pressure boiler, heat from the process gas is used to
produce low-pressure steam. Because chlorides in the boiling water
may induce stress-corrosion cracking of the 300 series stainless steels,
the straight-chromium 400 series are a better choice. They are resistant
to both stress cracking and carbolic acid erosion/ corrosion.
If there is also a hot potassium carbonate reboiler, to remove car-
bon dioxide from the product stream, Type 304 stainless is usedagain
to resist the carbonic acid erosion/corrosion mechanism associated
with the wet process gas.
44

REFERENCES
1. Steel Products Manual-Stainless and Heat Resisting Steels, American Iron
and Steel Institute, December 1974.
2. Simmons, W. F. and Gunia, R. B., ASTM Data Series DS 45, American
Society for Testing and Materials, 1969.
3. Polar, J. P., A Guide to Corrosion Resistance-304, 316, 317, '20', and Ni-O-
Nel, Climax Molybdenum Company, 1961.
4. Stainless Steel and the Chemical Industry, Climax Molybdenum Company,
1966.
5. Parker, T. D. and Briggs, J. Z., Ways to Bridge the Experience Gap, METAL
PROGRESS, September 1967, pp. 106.
6. Stainless Steel Industry Data* 7. Stainless Steel Industry Data* 8. Stainless
Steel Industry Data* 9. Stainless Steel Industry Data* 10. Kopecki, E. S.,
CHEMICAL ENGINEERING, January 22, 1973, pp. 124.
11. Loginow, A. W. and Bates, J. F., 18-18-2, MATERIALS PROTECTION AND
PERFORMANCE, May 1972, pp. 35.
12. Schneil, M., CORROSION HANDBOOK, (H. Uhlig, Editor), John Wiley and
Sons, 1948, pp. 181.
13. Bond, A. P., Marshall, J. D., and Dundas, H. J., STP No. 425, American
Society for Testing and Materials, 1968, pp. 116.
14. Steigerwald, R. F., TAPPI, Vol. 56, No. 4, April 1973, pp. 129-133.
15. Steigerwald, R. F., MATERIALS PERFORMANCE, Vol. 13, No. 9, September
1974, pp. 9-16.
16. Binder, W. O. and Spindelow, H. R., Transactions American Society for
Metals, 43:759, 1951.
17. Stainless Steel Industry Data* 18. Stainless Steel Industry Data* 19. Stainless
Steel Industry Data* 20. Stainless Steel Industry Data 21. Stainless Steel
Industry Data* 22. Corrosion Resistance of the Austenitic Chromium-Nickel
Stainless Steels in High-Temperature Environments, The International Nickel
Company, 1963. 23. McAllister, R. A., Eastham, D. H., Dougharty, N. A., and
Hollier, M., A Study of Scaling and Corrosion in Condenser Tubes Exposed
to River Water, CORROSION, Vol. 17, No. 12, 1961, pp. 579t-588t.
24. Schrieber, C.F., Boyce, T. D., and Oakes, B. D., Behavior of Metals In
Desalting Environments-Sixth Progress Report, NACE Paper No. 139, March
1974.
25. Anon. Solving the Corrosion Problem in Sugar Refineries, MATERIALS
PROTECTION AND PERFORMANCE, September 1972, pp. 52-53.
26. Fyfe, D., Sanz, D., Jones, F. W. S., and Cameron, G. M., Anodic Protection
of Sulfuric Acid Plant Cooling Equipment. NACE Paper No. 63, April 1975.
27. Cooper, A. S., STP 534, American Society for Testing and Materials,
1973, pp. 42.
28. Corrosion Data Survey, National Association of Corrosion Engineers, 1967.
29. Corrosion by Some Organic Acids, CORROSION, Vol. 8, No. 1, 1952,
pp. 14-28.
30. Groves, N. D. et al, Corrosion of Metals by Weak Acids Under Heat Transfer
Conditions, CORROSION, Vol. 17, No. 4, 1961, pp. 173t.
* Stainless Steel Industry Data.
For additional information on alloys or
applications referenced, write to:
Committee of Stainless Steel Producers
American Iron and Steel Institute
1000 16th Street, N.W.
Washington, D.C. 20036
ACKNOWLEDGEMENT
The Committee of Stainless Steel
Producers acknowledges the data and
photographs received from the following:
Brighton Corporation
Davy Powergas Inc.
Fluor Corporation
National Association of Corrosion Engineers
Struthers Wells Corporation
Texas Instruments
E. A. Tice Associates Tranter Mfg. Inc.
L. S. VanDelinder, P.E.
Votator Division Chemetron Corporation

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