1.

1- Definition of Corrosion
Corrosion may be defined as a destructive phenomena, chemical or
electrochemical, which can attack any metal or alloy through reaction by the
surrounding environment and in extreme cases may cause structural failure.
Corrosion can be also defined as the deterioration of material by reaction to its
environment. The corrosion occurs because of the natural tendency for most
metals to return to their natural state; e.g., iron in the presence of moist air will
revert to its natural state, iron oxide. Metals can be corroded by the direct
reaction of the metal to a chemical; e.g., zinc will react with dilute sulfuric acid,
and magnesium will react with alcohols.
1.2- Importance of Corrosion Studies
The importance of corrosion studies is two folds. The first is economic,
including the reduction of material losses resulting from the wasting away or
sudden failure of piping, tanks, metal components of machines, ships, hulls,
marine, structures…etc. The second is conservation, applied primarily to metal
resources, the world’s supply of which is limited, and the wastage of which
includes corresponding losses of energy and water resources accompanying the
production and fabrication of metal structures.
1.3- Basic Causes of Corrosion
1.3.1- Conditions necessary for corrosion
For the purpose of this manual, electrochemical corrosion is the most
important classification of corrosion. Four conditions must exist before
electrochemical corrosion can proceed:
1- There must be something that corrodes (the metal anode).
2- There must be a cathode.
3- There must be continuous conductive liquid path (electrolyte, usually
condensate and salt or other contaminations).
4- There must be a conductor to carry the flow of electrons from the anode
to the cathode. This conductor is usually in the form of metal-to-metal
contact such as in bolted or riveted joints.
The elimination of any one of the four conditions will stop corrosion.
1.3.2- Effect of material selection
One of the fundamental factors in corrosion is the nature of the material.

1
Materials are usually selected primarily for structural efficiency, and corrosion
resistance is often a secondary consideration in design.
1.3.3- Water intrusion
Water intrusion is the principal cause of corrosion problems encountered
in the field use of equipment. Water can enter an enclosure by free entry,
capillary action, or condensation. With these three modes of water entry acting
and with the subsequent confinement of water, it is almost certain that any
enclosure will be susceptible to water intrusion.
1.3.4- Environmental factors
At normal atmospheric temperatures the moisture in the air is enough to
start corrosive action. Oxygen is essential for corrosion to occur in water at
ambient temperatures. Other factors that affect the tendency of a metal to
corrode are:
1- Acidity or alkalinity of the conductive medium (pH factor).
2- Stability of the corrosion products.
3- Biological organisms (particularly anaerobic bacteria).
4- Variation in composition of the corrosive medium.
5- Temperature.
The corrosion problem at KSC is complex. The presence of salts and
acids on metal surfaces greatly increases the electrical conductivity of any
moisture present and accelerates corrosion. Moisture tends to collect on dirt
particles.

1.4- Classification of Corrosion

All metallic materials consist of atoms having valiancy electrons which can
be donated or shared. In a corrosive environment the components of the metallic
material get ionized and the movement of the electrons sets up a galvanic or
electrochemical cell which causes oxidation, reduction, dissolution or simple
diffusion of elements.
The metallurgical approach of corrosion of metals is in terms of the nature
of the alloying characteristics, the phases existing and their inter-diffusion under
different environmental conditions. In fact, the process of corrosion is a complex
phenomenon and it is difficult to predict the exclusive effect or the individual
role involved by any one of the above mentioned processes.
Based on the above processes, corrosion can be classified in many ways as
low temperature and high temperature corrosion, direct oxidation and
electrochemical corrosion, etc. The preferred classification is:
Dry or chemical corrosion and wet or electrochemical corrosion.

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 1- Chemical corrosion: In which the metal is converted into its oxide
when the metal is exposed to a reactive gas or non-conducting liquids.
2- Electrochemical corrosion: The formation of hydrous oxide film occurs
when the metal is immersed in a conducting liquid containing dissolved
reactive substance. The reaction is considered to take place at the metal-
solution interface, due to the heterogeneity on the metal surface, which
creates local anodic and cathodic sites on the metal.
1.5- Factors Influence Corrosion
The nature and extent of corrosion depend on the metal and the
environment. The important factors which may influence the corrosion process
are:
a) Nature of the metal, nature of the environment and the corrosion products.
b) Temperature. c) Concentration of electrolyte.
d) Electrode potential. f) Aeration. g) Agitation.
h) Hydrogen over voltage and pH of the electrolyte.

1.6- Theories of Corrosion

The corrosion of metals in aqueous solutions is an electrochemical
process as established in the first half of the 19th century. Whitney [1] gave the
most acceptable electrochemical theory. The other theories such as acid theory
[2], chemical attack theory, colloidal theory [3, 4] and biological theory [5]
were Proved to form apart of electrochemical theory.

1.6.1- Electrochemical theory of corrosion

Electrochemistry is a branch of chemistry dealing with relationships
between electricity and chemical reactions. It involves oxidation and reduction
(redox) reactions. Corrosion is an example of a type of electrochemical reaction,
since a substance -oxidizing agent- oxidizes a metal in its environment. In the
natural environment, oxygen gas is a good oxidizing agent. Most metals have
lower reduction potentials than O2; therefore they are easily oxidized in the
presence of oxygen. Metals such as gold, silver and platinum are not so easily
oxidized and are sometimes referred to as noble metals. The reasons for the lack
of oxidation in these noble metals are varied and sometimes complex.
One of the most familiar corrosion processes is the oxidation of iron
(rusting). Iron metal is spontaneously oxidized in the presence of O 2 and an
aqueous electrolyte solution. Physical strains (scratches, dents, bends, etc…)
present on the iron are more easily oxidized than other areas. This directly
relates to physics, i.e., the way electric fields are generated at the surface of the

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metal. Stronger fields are generated at the physically strained parts of the metal.
The result is that these regions are anodic (oxidation occurs) and simultaneously
different areas are cathodic regions at which a reduction reaction (usually of O 2)
occurs.
The iron atom gives up two electrons to form the Fe2+ ion:
Fe(s) Fe2+(aq) + 2e- (anodic) (1.1)
The electrons that are released flow through the iron metal to the cathodic region
where they react with oxygen:
O2(g) + 2H2O(l) + 4e-  4OH-(aq) (cathodic) (1.2)

Fig. (1.1): The basic corrosion cell consists of an anode, a cathode, an

electrolyte, and a metallic path for electron flow.
These two half reactions together give the overall reaction:
Fe(s) + 1/2O2(g) + H2O(l) Fe2+(aq) + 2OH-(aq) (1.3)
Common experience with this process (e.g., car fenders) tends to show that Fe2+
is eventually oxidized further to Fe3+, in the compound iron (III) oxide (rust):
4Fe2+(aq) + O2(g) + 4H2O(l) 2Fe2O3(s, red colour) + 8H+(aq) (1.4)
In the experimental setup, this last reaction does not occur. The Fe2+(aq) reacts
with [Fe(CN)6]3- in the gel, forming Fe[Fe(CN)6]-, which is a vivid blue colour.
The gel you use contains phenolphthalein, an indicator that is pink in basic
solutions. Since the reduction of O2 results in a basic solution, one will observe a
pink colour at the cathodic region. Thus, phenolphthalein and [Fe(CN) 6]3- are
used to show where the cathodic and anodic regions are.
Further complications arise if we have a system where two different
metals are in contact with each other, both in the electrolyte solution. Consider
iron metal in contact with another metal. When this situation is encountered,
electric fields are set up due to the difference in the reduction potential of the
two metals. These fields are stronger than any effect caused by physical strains.
Thus, one metal will act entirely as the anode, while the other becomes the

4
cathode. One can use standard reduction potentials to determine which metal
will act as the anode/cathode.
When considering a bimetallic system, the metal with the more positive
reduction potential will be reduced (cathode) and the metal with the more
negative reduction potential will be oxidized (anode). For example, if copper
and zinc were connected electrically and immersed in an electrolyte solution, we
might expect that the copper would be the cathode and the zinc the anode, based
on their relative reduction potentials.

1.6.2- Effects of the anode and cathode areas on the corrosion process
Area Effects are important, especially in galvanic and localized corrosion.
Consider the difference between a cell with a very large anode area compared to
the cathode and one in which the cathode is significantly larger than the anode.
Since metal is corroded at the anode only, the rate of corrosion will be
proportional to the rate at which the anodic reaction proceeds. For the anodic
reaction to proceed, however, there must be corresponding cathodic reactions.
The cathodic reaction therefore controls the rate of the overall reaction. With a
large cathode and a small anode, there is more surface area on which cathodic
reactions may proceed so the anodic reaction proceeds at a much faster rate than
if the reverse (i.e. large anode, small cathode) is true. Where use of dissimilar
metals is unavoidable, therefore, it is desirable to use the more noble (cathodic)
metal in the smallest possible exposed area relative to the anode.
1.7- Thermodynamic Principles of Corrosion
Corrosion resistance or chemical resistance depends on the following:
1- Thermodynamic principles.
2- Physical and chemical factors.
3- Metallurgical factors.
4- Electrochemical principles.
Thermodynamic and electrochemical principles play a major role in
determining the corrosion behavior of materials.
Thermodynamic indicates the spontaneous direction of a chemical
reaction. It is used to determine whether or not corrosion is theoretically
possible.
Almost all metals and alloys used in service are actually in an unstable
thermodynamic state. There is thus a fundamental thermodynamic tendency for
them to return to a stable state through corrosion processes. Thermodynamics is
concerned with energy states. The original metallic ores are said to be in a state
of low energy. External energy is applied in the conversion of the ores to usable

5
metals and alloys, transforming them to a higher energy state. They tend to
revert to a lower (more stable) energy state by reacting with a corrosive
environment. While thermodynamics can predict whether a corrosion reaction
will take place, it does not provide an indication of the rate of corrosion
reactions [6,7].
For a reaction to be occurred spontaneously there must be a free energy
change, ΔG, and since the energy, in the case of spontaneous reaction, is given
out, the sign is negative. The magnitude of the ΔG and its sign are of great
importance, since it indicates whether or not the corrosion reaction will take
place. For example the following reaction of aluminium in hydrochloric acid:
Al + 3HCl AlCl3 + 3/2H2 (1.5)
The reaction is thermodynamically favorable; i.e. free energy change ΔG must
be negative. This reaction can be divided into anodic half and cathodic half
reactions as follows:
Al Al3+ + 3e- (Anodic half reaction) (1.6)
3HCl + 3e-  3/2H2 + 3Cl- (Cathodic half reaction) (1.7)
These two half reactions have associated free energy change, thus, overall, the
sum of the two free energies change must be negative, i.e.
ΔGanodic + ΔGcathodic < 0
where:
ΔGanodic is the free energy change for anodic iron dissolution.
ΔGcathodic is the free energy change for cathodic hydrogen evolution.
The electrical potential, can be related to the free energy change by the
following equation:
ΔG = -n F E (1.8)
where:
ΔG is the free energy change.
n is the number of electrons transferred in the half-cell reaction.
F is the charge transported by 1 mole of electrons and has the value of
96494 coulombs/mole.
E is the measured potential in volts (Vs. SHE).
Similarly,
ΔGo = -n F Eo (1.9)
where:
ΔG˚ is the standard free energy change.
n and F are defined as above.

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 E˚ is the standard electrode potential and can be obtained from
thermodynamic tables.
Al  Al3+ + 3e- Eo = 1.7V (1.10)
Under nonstandard conditions i.e., the respective ions not at unit activity, the
electrode potential is related to the standard electrode potential by Nernst
equation [8].
E = Eo + (RT/ nF) ln (aOx/ aRed) (1.11)
As can be seen from this equation the activity of the oxidized species (a Ox)
increases as electrode potential (E) becomes more positive. In aqueous
environments the thermodynamic consideration of electrochemical corrosion
was the bases of the construction of (E)- pH diagram, which are also known as
Pourbaix diagram [9]. Such diagrams are essentially isothermal phase diagrams,
which represent metal-ion/ oxide equilibrium plotted with potential, and pH bas
coordinates [10].
1.8- Types of Corrosion
1.8.1- General or uniform corrosion
Differences in electrical potential occur on the surface of a piece of metal
due to small differences in chemical composition, phase differences, amount of
cold work, etc. These differences set up small corrosion cells each with an anode
and cathode. Corrosion continues until the metal is consumed or the film of rust
formed on the surface sets up a barrier to the electrolyte.
1.8.2- Pitting corrosion
Pitting corrosion is a complex but important problem that is at the root of
many corrosion failures. It has been studied in detail for many years, yet crucial
phenomena remain unclear. In pitting corrosion the surface of the metal is
attacked in small-localized areas. Organisms in water or breaks in a passive film
can initiate corrosion. In pitting corrosion very little metal is removed from the
surface but the effect is marked.
In passivated metals or alloys that are exposed to solutions containing
aggressive anions, primarily chloride, pitting corrosion results in local
dissolution leading to the formation of cavities or (holes). The shape of the pits
or cavities can vary from shallow to cylindrical holes and the cavity is
approximately hemispherical [11]. The pit morphology depends on the
metallurgy of the alloy and chemistry of the environment as well as the leading
conditions. As observed first by McAdam in 1928, these pits may cause local
increase in stress concentration and cracks may nucleate from them.

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 Pitting corrosion occurs mostly in solutions containing halide or
oxyhalides. Chlorides, bromides and hypochlorites are the most aggressive
anions [12]. Fluoride, iodide and iodine containing anions were thought to be
without pitting tendency. However, iodide ions were found to cause pitting
corrosion in many cases [13]. Solutions of certain oxidizing cations produce the
worst pitting attack. Ferric, cupric and mercuric halides are the most aggressive
of all pitting reagents. The non-oxidizing metal halides such as Al, Ca and Na
cause pitting to a lesser degree.
Electrochemical studies of pitting corrosion have found that there exist
characteristic potentials. Stable pits form at potentials noble to the pitting
potential, EP, and will grow at potentials noble to the repassivation potential,
ER, which is lower than EP. During upward scanning in a cyclic polarization
experiment, a stable pit starts growing at EP where the current increases sharply
from the passive current level and, upon reversal of the scan direction,
repassivates at ER where the current drops back. It is generally considered that
materials exhibiting higher values of EP and ER are more resistant to pitting
corrosion, and cyclic polarization experiments are commonly used for this
purpose.
Pitting is considered to be autocatalytic in nature; once a pit starts to
grow, the conditions developed are such that further pit growth is promoted. The
anodic and cathodic electrochemical reactions that comprise corrosion separate
spatially during pitting. The local pit environment becomes depleted in cathodic
reactant (e.g. oxygen), which shifts most of the cathodic reaction to the boldly
exposed surface where this reactant is more plentiful. The pit environment
becomes enriched in metal cations and an anionic species such as chloride,
which electromigrates into the pit to maintain charge neutrality by balancing the
charge associated with the cation concentration. The pH in the pit is lower
owing to cation hydrolysis and the absence of a local cathodic reaction. The
acidic chloride environment thus generated in pits is aggressive to most metals
and tends to propagate the pit growth.
1.8.3- Stress corrosion cracking
Failure is due to the simultaneous influence of static tensile stresses and a
corrosive environment and this is specific to a particular metal. The stresses may
be internal such as those caused by cold work, welding, heat treatment or
external forces caused by mechanical stresses set up by assembly practices. A
good example of this form of corrosion is 316 stainless steel in marine
environments. 316 stainless steel was developed to withstand attacks in chloride
environments, but if stressed the steel will fail by stress corrosion cracking.
1.8.4- Intergranular corrosion

8
 Corrosion occurs at the grain boundaries due to a difference in potential
between the anodic grain boundaries and the cathodic grains. "Sensitized"
stainless steels, where carbides have been precipitated in the grain boundaries
during improper heat treatment or in the heat-affected zone of a weld, are
particularly susceptible to intergranular corrosion.
1.8.5- Corrosion fatigue
Failure under repeated cycling stresses in a corrosive environment.
1.8.6- Filiform corrosion
Filiform corrosion appears as a network of corrosion trials, of a wormlike
structure, particularly beneath thin organic coatings. Salts containing chlorides,
which have been left on the surface prior to coating, are suspected.
1.8.7- Crevice corrosion
Crevice corrosion occurs when there is a difference in ion, or oxygen,
concentration between the metal and its surroundings. Oxygen starvation in an
electrolyte at the bottom of a sharp V-section will set up an anodic site in the
metal that then corrodes rapidly.
1.8.8- Galvanic or bi-metallic corrosion
Galvanic corrosion takes place between two different metals, or coatings,
which are joined together in the presence of an electrolyte. Each metal has a
potential different from any other metal when placed in an electrolyte. A series
can be built up of all the metals relative to each other.
1.8.9- Fretting corrosion
Fretting corrosion occurs when two or more parts rub against each other.
The rubbing action removes the corrosion products and exposes new metal to
the electrolyte.
1.8.10-Erosion corrosion
Erosion is the removal of metal by the movement of fluids against the
surface. The combination of erosion and corrosion can provide a severe rate of
corrosion.

1.8.11-Selective leaching or demetalification

Demetalification is the removal of one of the alloying elements in an alloy
by the electrolyte. This results in a "spongy" metal. Typical example is the
removal of zinc in chloride waters from brass.
1.9- Cost of Corrosion

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 Corrosion is not only dangerous, but also costly, with annual damages in
the billions of dollars! If this is difficult to believe, consider some of the direct
and indirect effects of corrosion which contribute to these costs:
1- Replacement of corroded equipment.
2- Unscheduled plant shutdowns for replacement.
3- Process upsets resulting from corrosion.
4- Product contamination.
5- Product loss from a vessel that has corroded.
6- Otherwise unnecessary preventive maintenance.
7- Over design to allow for corrosion.
8- Inability to use otherwise desirable materials.
While the economic costs are frightening, we must consider them to be of
secondary importance to the potential loss of life and damage to the environment
problems, which can have widespread effects upon modern industrial
businesses. It is essential, therefore, for operators of industrial process plants to
have a program for controlling corrosion.
1.10- Methods of Corrosion Protection
1.10.1- Application of protective coatings
Metallic structures can be protected from corrosion in many ways. A
common method involves the application of protective coatings made from
paints, plastics or films of noble metals on the structure itself (e.g., the coating
on tin cans). These coatings form an impervious barrier between the metal and
the oxidant but are only effective when the coating completely covers the
structure. Flaws in the coating have been found to produce accelerated corrosion
of the metal.
1.10.2- Polarize or shift the potential of the metal
Another method of reducing corrosion is to polarize or shift the potential
of the metal enabling it to act as a cathode (rather than an anode) in an
electrochemical cell. One example is the galvanizing of steel with a coating of
zinc. The iron and zinc then function as the electrodes of a cell. Zinc is the more
readily oxidized metal of the pair and functions as the anode and corrodes, while
the iron functions as the cathode. The zinc is used up and protection is effective
as long as some zinc remains. Sacrificial anodes work on the same principal but
use an external electrode made from a readily oxidized metal; this form of
protection is commonly used on buried pipelines.
1.10.3- Cathodic protection
Cathodic protection using an impressed current derived from an external
power supply is a related form of protection in which the metal is forced to be

10
the cathode in an electrochemical cell. For example, most cars now use the
negative terminal on their batteries as the ground. Besides being a convenient
way to carry electricity, this process shifts the electrical potential of the chassis
of the car, thereby reducing (somewhat) its tendency to rust.
1.10.4- Materials selection
Basic recommendations for eliminating corrosion are materials selection
which are summarized as follows:
1- Use corrosion-resistant materials including plastics and non-metallics in
severe environments.
2- Avoid dissimilar metal couples.
3- Avoid the use of back-to-back structural shapes, such as boxbeam
sections and unistrut. When the exterior use of unistrut cannot be avoided,
selection of appropriate material shall be considered, such as stainless
steel. In addition, alternate structural shapes shall be considered such as
C- or d-shaped channel, especially in highly corrosive areas.
4- Avoid the use of alloys susceptible to stress-corrosion.
1.10.5- Corrosion inhibitors
Corrosion inhibitors can be added to solutions in contact with metals (e.g.
inhibitors are required in the antifreeze solution in automobile cooling systems).
These compounds can prevent either the anode or the cathode reaction of
corrosion cells; one way that they can do this is by forming insoluble films over
the anode or cathode sites of the cell. Examples of anodic inhibitors are sodium
phosphate or sodium carbonate while zinc sulfate and calcium or magnesium
salts act as cathodic inhibitors. New forms of paints are being developed which
take advantage of similar properties. These paints promise to nearly eliminate
corrosion in applications like painted car fenders, etc.
1.11- Corrosion Inhibitors
1.11.1-Corrosion inhibition in acid solutions
Acid solutions are widely used in industry, where the most important
fields of application are acid pickling, industrial acid cleaning and oil well
acidizing. Because of general aggressively of acid solutions, the practice of
inhibition is commonly used to reduce the corrosive attack on metallic materials.
The selection of appropriate inhibitors mainly depends on the type of
acid, its concentration, temperature and velocity of flow, the presence of
dissolved organic and/or inorganic substances, and on the type of metallic
material exposed to the action of acidic solution.
Most of well-known acid inhibitors are organic compounds containing
nitrogen, sulphate and oxygen [14-21].

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1.11.2-Factors affecting inhibitors action in aggressive acid media
a- Interaction of the inhibitor with a metal surface
Physical (or electrostatic) adsorption and chemisorption are the principle
types of interaction between an organic inhibitor and a metal surface.
i- Physical adsorption
Physical adsorption is the result of electrostatic attractive forces between
inhibiting ions or dipoles and the electrically charged surface of the metal. The
surface charge of the metal is due to the electric field at the outer Helmhaltz
plane of the electrical double layer existing at the metal/solution interface. The
surface charge can be defined by the potential of the metal E corr vs. its zero
charge potential (ZPC) (Eq=o) [22] when the difference Ecorr - Eq = ф is negative
charge, cation adsorption is favored. Adsorption of anions is favored when ф
become positive. This behaviour is related not only to positively or negatively
charged compounds, but also to dipoles whose orientation is determined by the
value of the ф potential.
According to Antropov [22], at equal value of ф for different metals,
similar behaviour of gives inhibiting species should be expected in the same
environment.
In study the adsorption of ions at the metal/solution interface, it was first
assumed that ions maintained their total charge during the adsorption. Giving
rise in this way to a pure electrostatic bond. Lorenz [23-25] suggested that
partial charge is present in the adsorption of ions; in this case a certain amount
of covalent bond in the adsorption process must be considered. The partial
charge concept studied by Shultz and Kappitz [26] and others [27-29], they
defined electrosorption valency as the coefficient for the potential dependence
and charge flow of electrosorption process. The term electrosorption valency
was chosen because of its analogy with the electrode reaction valency, which
enters into Faraday’s law as well as the Nernest equation.
ii- Chemisorption
Another type of metal/inhibitor interaction is chemisorption. This process
involves charge sharing or charge transfer from the inhibitor molecule to the
metal surface in order to form a coordinate type of bond.
The chemisorption process takes place more slowly than electrostatic
adsorption and with higher activation energy. It depends on the higher
temperature; higher degree of inhibition should be expected at higher
temperature.
Chemisorption is specific for certain metals and is not completely
reversible [28]. The bonding occurring with electron transfer clearly depends on

12
the nature of the metal and the nature of organic inhibitor. In fact, electron
transfer is typical for transition metals having vacant, low-energy electron
orbitals.
The structure characteristics of the rest of the molecule influence the
electron density on the heteroatom and as a consequence, the strength of the
chemisorption bond. Regular and systematic changes in the molecular structure,
such as the introduction of substituents in various positions on the aromatic and
heterocyclic compounds, may influence the electron density and the ability of
compounds to inhibit corrosion.
Relationship between electronic structure and efficiency of various
classes of inhibitors has been deduced from quantum mechanical calculations
[30-33]. In this way, the electron density, the order of the bond along the bond
line, the index of free valence and the charge of atoms in the free and adsorbed
states have been calculated. Other structure parameters influencing the inhibiting
efficiency may be mentioned. Thus, the projected molecular area [34],
molecular weight [35] of various series of organic compounds has been
correlated with variation in inhibiting efficiencies.
b- Interaction between adsorbed inhibitors
When the coverage of the metal surface by adsorbed inhibitor species,
lateral interaction between inhibitor molecules may arise, influencing the
inhibition efficiency. Attractive lateral interactions usually give rise to stronger
adsorption and higher inhibition efficiency. This effect has been show in the
case of compounds containing long hydrocarbon chains due to attractive Vander
Waals forces [36,37]. In the presence of ions or molecules containing dipoles,
repulsive interaction may occur, weakling the adsorption and diminishing the
inhibition efficiency.
c- Interaction of the inhibitor with water molecules
Due to adsorption process of an inhibitor, water molecules are being
removed from the metal surface. During the adsorption process of a molecule
the interaction energy between molecule and water changes as it passes from the
dissolved to adsorbed state. This change forms an important part of the free
energy of adsorption, i.e., the higher the solvation energy of the adsorpting
species, the higher the free energy of adsorption. Increasing the size of the
hydrocarbon portion of an organic molecule will increase the solvation energy
of an inhibitor leading to decrease the solubility and increasing absorbability
[38].
d- Relationship between inhibitor reactivity and efficiency

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 The nature of the inhibitor initially present in acid solutions may change
with the time and/or the electrode potential as a consequence of reduction
reactions, polymerization reactions, or formation of surface products. The
inhibition due to the reaction products is usually called secondary inhibition,
whereas primary inhibition may be higher or lower than secondary inhibition,
depending on the effectiveness of the reaction product [39].
1.11.3-Adsorption isotherms
The adsorption isotherms describe the relation ship between the coverage
(θ) of an interface with adsorbed species and concentration of the species in
solution. Various adsorption isotherms have been listed as follow [40,41]:
a- The Henry isotherm: It has the following form:
θ=KC (1.12)
where:
K is the adsorption equilibrium constant.
C is the concentration of the adsorbate in the bulk phase in moles / liter.
θ is the degree of surface coverage.
b- The Freundlich isotherm: It has the following form:
θ = K Cn (1.13)
where:
K and C are defined as in Henry isotherm.
n is a constant where, 0 < n < 1.
c- The Langmiur isotherm: It has the following form:
θ/ 1- θ = K C (1.14)
d- The Volmer isotherm: It has the following form:
K C = θ/ 1 - θ exp (θ/ 1 - θ) (1.15)
e- The Amagat isotherm: It has the following form:
K Cn = θ/ 1 - θ exp (θ/ 1 - θ) (1.16)
which has the same form as the Volmer isotherm but the concentration is raised
to the power n where, 0 < n < 1.
f- The Frumkin isotherm: It has the following form:
K C = θ/ 1 - θ exp (-2 a θ) (1.17)
where:
a is a parameter characterizing the interaction between the adsorbed
particles..
a > 0, Attraction while a < 0, Repulsion.

14
g- The Parsons isotherm: It has the following form:
K C = θ/ 1 - θ exp ((2 - θ / (1 - θ )2 - 2 a θ) (1.18)
h- The Temkin isotherm: It has the following form:
ln K C = a θ (1.19)
where all terms are defined as described above and θ varies between
0.1 < θ < 0.9.
Interpretation of adsorption and performance of organic inhibitors can be
evidenced by fitting the data to one of the adsorption isotherms.
1.12- Corrosion Monitoring
1.12.1-Definition of corrosion monitoring
Corrosion monitoring (measurement) is the quantitative method by which
the effectiveness of corrosion control and prevention techniques can be
evaluated and provides the feedback to enable corrosion control and prevention
methods to be optimized. Corrosion measurement employs a variety of
techniques to determine how corrosive the environment is and at what rate metal
loss is being experienced.
1.12.2-Corrosion monitoring techniques
A large number of corrosion monitoring techniques exist. The following
list details the most common techniques, which are used in industrial
applications:
a. Corrosion coupons (weight loss)
The weight loss technique is the best known and simplest of all corrosion
monitoring techniques. The method involves exposing a specimen of material
(the coupon) to a process environment for a given duration, then removing the
specimen for analysis. The basic measurement which is determined from
corrosion coupons is weight loss; the weight loss taking place over the period of
exposure being expressed as corrosion rate.
The simplicity of the measurement offered by the corrosion coupon is
such that the coupon technique forms the baseline method of measurement in
many corrosion monitoring programs.
Advantages of weight loss coupons are that:
 The technique is applicable to all environments- gases, liquids, and solids/
particulate flow.
 Visual inspection can be undertaken.
 Corrosion deposits can be observed and analyzed.

15
  Weight loss can be readily determined and corrosion rate easily
calculated.
 Localized corrosion can be identified and measured.
 Inhibitor performance can be easily assessed.
The disadvantage of the coupon technique is that:
 If a corrosion upset occurs during the period of exposure, the coupon
alone will not be able to identify the time of occurrence of the upset, and
depending upon the peak value of the upset and its duration, may not even
register a statistically significant increased weight loss
Therefore, coupon monitoring is most useful in environments where
corrosion rates do not significantly change over long time periods. However,
they can provide a useful correlation with other techniques such as E/R and LPR
measurements.
b- Electrical resistance (E/R™) monitoring
E/R probes can be thought of as "electronic" corrosion coupons. Like
coupons, E/R probes provide a basic measurement of metal loss, but unlike
coupons, the value of metal loss can be measured at any time, as frequently as
required, while the probe is in-situ and permanently exposed to the process
stream.
The E/R technique measures the change in Ohmic resistance of a
corroding metal element exposed to the process stream. The action of corrosion
on the surface of the element produces a decrease in its cross-sectional area with
a corresponding increase in its electrical resistance. The increase in resistance
can be related directly to metal loss and the metal loss, as a function of time is
by definition the corrosion rate.
E/R probes have all the advantages of coupons, plus:
 Probe remains installed in-line until operational life has been exhausted.
 They respond quickly to corrosion upsets and can be used to trigger an
alarm.
 The response time for E/R monitoring is far shorter than that for weight
loss coupons.
 E/R probes are available in a variety of element geometries, metallurgies
and sensitivities and can be configured for flush mounting such that
pigging operations can take place without the necessity to remove probes.
The range of sensitivities allows the operator to select the most dynamic
response consistent with process requirements.
c- Linear polarization resistance (LPR) monitoring

16
 The LPR technique is based on complex electro-chemical theory. For
purposes of industrial measurement applications it is simplified to a very basic
concept. In fundamental terms, a small voltage (or polarization potential) is
applied to an electrode in solution. The current needed to maintain a specific
voltage shift (typically 10mV.) is directly related to the corrosion on the surface
of the electrode in the solution. By measuring the current, a corrosion rate can be
derived.
Advantages of the LPR technique are that:
 The measurement of corrosion rate is made instantaneously.
 This is a more powerful tool than either coupons or E/R where the
fundamental measurement is metal loss and where some period of
exposure is required to determine corrosion rate.
Disadvantages of the LPR technique are that:
 It can only be successfully performed in relatively clean aqueous
electrolytic environments.
 It will not work in gases or water/ oil emulsions where fouling of the
electrodes will prevent measurements being made.
d- Galvanic/potential monitoring
The galvanic monitoring technique, also known as Zero Resistance
Ammetry (ZRA) is another electrochemical measuring technique. With ZRA
probes, two electrodes of dissimilar metals are exposed to the process fluid.
When immersed in solution, a natural voltage (potential) difference exits
between the electrodes. The current generated due to this potential difference
relates to the rate of corrosion, which is occurring on the more active of the
electrode couple.
Galvanic/Potential monitoring is applicable to the following electrode couples:
 Bimetallic corrosion.
 Crevice and pitting attack.
 Corrosion assisted cracking.
 Corrosion by highly oxidizing species.
 Weld decay.
 Galvanic current measurement has found its widest applications in water
injection systems where dissolved oxygen concentrations are a primary
concern. Oxygen leaking into such systems greatly increases galvanic
currents and thus the corrosion rate of steel process components. Galvanic
monitoring systems are used to provide an indication that oxygen may be
invading injection waters through leaking gaskets or deaeration systems.
e- Specialized monitoring

17
 i- Biological monitoring
Biological monitoring and analysis generally seeks to identify the
presence of Sulphate Reducing Bacteria- SRB's. This is a class of anaerobic
bacteria which consume sulphate from the process stream and generate sulphuric
acid, a corrosive which attacks production plant materials.
ii- Sand/ erosion monitoring
These are devices, which are designed to measure erosion in a flowing
system. They find wide application in oil/gas production systems where
particulate matter is present.
iii- Hydrogen penetration monitoring
In acidic process environments, hydrogen is a by-product of the corrosion
reaction. Hydrogen generated in such a reaction can be absorbed by steel
particularly when traces of sulphide or cyanide are present. This may lead to
hydrogen-induced failure by one or more of several mechanisms. The concept of
hydrogen probes is to detect the amount of hydrogen permeating through the
steel by mechanical or electrochemical measurement and to use this as a
qualitative indication of corrosion rate.
1.13- Corrosion inhibition of C- steel in acidic solutions
1.13.1-Uses of C- steel

Steel is a metal alloy whose major component is iron, with carbon content
between 0.02% and 1.7% by weight. Carbon is the most cost effective alloying
material for iron, but many other alloying elements are also used. Carbon and
other elements act as a hardening agent, preventing dislocations in the iron atom
crystal lattice from sliding past one another. Varying the amount of alloying
elements and their distribution in the steel controls qualities such as the
hardness, elasticity, ductility, and tensile strength of the resulting steel. Steel
with increased carbon content can be made harder and stronger than iron, but is
also more brittle. The maximum solubility of carbon in iron is 1.7% by weight,
occurring at 1130° Celsius; higher concentrations of carbon or lower
temperatures will produce cementite which will reduce the material's strength.
Alloys with higher carbon content than this are known as cast iron because of
their lower melting point. Steel is also to be distinguished from wrought iron
with little or no carbon, usually less than 0.035%. It is common today to talk
about 'the iron and steel industry' as if it were a single thing; it is today, but
historically they were separate products. Steel is often classified by its carbon
content: a high-carbon steel is serviceable for dies and cutting tools because of
its great hardness and brittleness. low- or medium-carbon steel is used for
sheeting and structural forms because of its amenability to welding and tooling.

18
C- steel, also called plain carbon steel, is steel where the main alloying
constituent is carbon. The American Iron and Steel Institute (AISI) defines
carbon steel as: "Steel is considered to be carbon steel when no minimum
content is specified or required for chromium, cobalt, columbium, molybdenum,
nickel, titanium, tungsten, vanadium or zirconium, or any other element to be
added to obtain a desired alloying effect; when the specified minimum for
copper does not exceed 0.40 percent; or when the maximum content specified
for any of the following elements does not exceed the percentages noted:
manganese 1.65, silicon 0.60, copper 0.60. The term "carbon steel" may also be
used in reference to steel which is not stainless steel; in this use carbon steel
may include alloy steels. Steel with a low carbon content has properties similar
to iron. As the carbon content rises, the metal becomes harder and stronger but
less ductile and more difficult to weld. In general, higher carbon content lowers
the melting point and its temperature resistance. Carbon content influences the
yield strength of steel because carbon atoms fit into the interstitial crystalline
lattice sites of the body-centered cubic (BCC) arrangement of the iron atoms.
The interstitial carbon reduces the mobility of dislocations, which in turn has a
hardening effect on the iron. To get dislocations to move, a high enough stress
level must be applied in order for the dislocations to "break away". This is
because the interstitial carbon atoms cause some of the iron BCC lattice cells to
distort. 85% of all steel used in the U.S. is carbon steel. Mild steel is the most
common form of steel because its price is relatively low while it provides
material properties that are acceptable for many applications. Low carbon steel
contains approximately 0.05–0.15% carbon and mild steel contains 0.16–0.29%
carbon, therefore it is neither brittle nor ductile. Mild steel has a relatively low
tensile strength, but it is cheap and malleable; surface hardness can be increased
through carburizing. It is often used when large quantities of steel are needed,
for example as structural steel. The density of mild steel is approximately
7.85 g/cm3 (0.284 lb/in3) and the Young's modulus is 210,000 MPa
(30,000,000 psi). Low carbon steels suffer from yield-point runout where the
material has two yield points. The first yield point (or upper yield point) is
higher than the second and the yield drops dramatically after the upper yield
point. If a low carbon steel is only stressed to some point between the upper and
lower yield point then the surface may develop Lüder bands.

1.13.2-Literature survey on corrosion of C- steel

In the following a concise literature survey on corrosion inhibition of C- steel
by some related organic compounds in acidic medium.

This article describes an investigation of the corrosion behavior of

carbon steel in 2 M HCl solution with the addition of some cyanoacetohydrazide

19
derivatives by weight loss, galvanostatic polarization, and potentiodynamic
anodic polarization techniques [42] . The explored methods gave almost similar
results. Results obtained reveal that inhibitor (I) is the best inhibitor and the
inhibition efficiency (IE%) follows the sequence I > II > III > IV. The
percentage inhibition efficiency was found to increase with increasing
concentration of inhibitors and decreases with increasing temperature of the
medium. The addition of KI, KSCN, and KBr to cyanoacetohydrazide
derivatives enhanced the inhibition efficiency due to synergistic effect. The
effect of temperature on C-steel corrosion in 2 M HCl and with the addition of
11 10-6 M of investigated compounds in the temperature range 30°-50°C was
studied. Some thermodynamic functions were computed and discussed. The
inhibitors are adsorbed on the carbon steel surface according to Temkin's
adsorption isotherm. Polarization data suggested that the additives used act as
mixed-type inhibitors. It was found that the cyanoacetohydrazide derivatives
provide good protection to carbon steel against pitting corrosion in chloride-
containing solutions.

2,6-Dimethylpyrimidine-2-amine and two of its derivatives have been

investigated [43] as corrosion inhibitors for carbon-steel (C-steel) in 2M HCl
solution using electrochemical impedance spectroscopy (EIS) and weight loss
techniques. The efficiency of the inhibitors increases with increase in the
inhibitor concentration. Results obtained reveal that the used pyrimidine
derivatives perform as corrosion inhibitors for C-steel in 2M HCl. Double layer
capacitance, Cdl, and charge transform resistance, Rct, values were derived from
Nyquist and Bode plots obtained from A.C. impedance studies. Change in
impedance parameters are indicative of the adsorption of these inhibitors on the
iron surface. The inhibition efficiency mainly depends on the nature of the
investigated compounds. The values of the inhibition efficiency calculated from
the two techniques are in reasonably good agreement. The adsorption of these
compounds on C-steel surface is found to obey Langmuir adsorption isotherm.
The mechanism of inhibition was discussed in the light of the chemical structure
of the undertaken inhibitors and their adsorption on C-steel surface.

The corrosion behavior of carbon steel in 1M HCl solution in the

absence and presence of three compounds of ethoxylated fatty amide was
studied [44] using weight loss and galvanostatic polarization techniques. The
percentage inhibition efficiency was found to increase with increasing of
inhibitor concentrations, number of ethylene oxide unit and with decreasing
temperature. The inhibitive action of these compounds was discussed in term of
adsorption on the steel surface through ethylene oxide unit while the
hydrocarbon parts protrude brush-like into the solution. The adsorption process

20
follows Langmuir adsorption isotherm. The effect of temperature on the rate of
corrosion in the absence and presence of these compounds was also studied.
Some activated thermodynamic parameters were calculated.

The effect of some mono azo dye compounds on the dissolution of

carbon steel (type L-52) in 2 M hydrochloric acid solution was studied [45]
using weight loss and galvanostatic polarization techniques The inhibition
efficiency was found to increase with increasing inhibitor concentration and
decreasing temperatures. Inhibition was explained by formation of insoluble
complex adsorbed on the metal surface. The adsorption follows Langmuir
adsorption isotherm. The formation of stable complex was studied by
conductometric titration. The stiochiometric ratio was found to be 1:1; 1:2 for
Fe2+/ dye compounds and the mechanism of inhibition was explained in terms
of these values. The thermodynamic functions of adsorption process was
calculated and discussed.

In the first part of this study, the inhibitor effect of single, binary and
ternary mixture of chromate, molybdate, nitrite, tetraborate, ortophosphate,
benzoate, acetate, ascorbic acid on the corrosion of carbon steel was investigated
[46]. Experiments were carried out in neutral aqueous solution containing 100
ppm Cl- at room temperature. The current-potential curves were obtained by
potentiostatic (1mV/s) method and the corrosion rates were determined by the
extrapolation of the Tafel slope of the cathodic polarization curves method and
linear polarization method. In the second part, the inhibitor effect of some one
component, binary and ternary inhibitor blends was investigated depending on
the temperature (30, 40, 50 oC) and pH (5, 7, 9). The inhibitor effects were
found to be %95 for solutions containing 50 ppm nitrite. Of all inhibitor systems
tried, chromatemolibdate and chromate- nitrite- molibdate was found to be the
most effective binary and ternary inhibitor blends, the effectiveness of which is
equal to that of sodium chromate, sodium nitrite, sodium molibdate that alone
and used at a high level.

1,12-bis(1,2,4-triazolyl)dodecane (dTC12) is an excellent corrosion

inhibitor for carbon steel in deaerated 1 M HCl solution. In this work
electrochemical and analytical techniques were used to study the inhibition of
corrosion on carbon steel in acidic medium. The carbon steel corrosion
inhibition of dTC12 was attributed to the synergistic effect between chloride
anion and quaternary ammonium ion. The protective efficiency of the film was
higher than 90%, indicating that corrosion of carbon steel in 1 M HCl is reduced
by dTC12. The effect of dissolved oxygen on the inhibition efficiency was also

21
investigated [47]. The results show that the inhibition efficiency increases in
early stage and decreases for a long immersion time.

The effect of some prepared compounds, namely pyridine derivatives on

the corrosion of carbon steel in 2 M HCl solutions has been studied [48] by
electrochemical polarization method (potentiodynamic, Tafel extrapolation) as
well as weight loss method. Generally, inhibition efficiency of the investigated
compounds was found to depend on the concentration and the nature of the
inhibitor. Results obtained from both potentiodynamic and weight loss
techniques reveal that these compounds are good inhibitors. The presence of
substitution in pyridine ring plays an important role in the percentage inhibition
of the compounds under investigation. The adsorption of these compounds on
the carbon steel follows a Langmuir adsorption isotherm.

The inhibition effect of novel nonionic surfactants on the corrosion of

carbon steel (CS) in 1 M HCl was studied [49] at different temperatures (20–
60 °C) by weight loss, electrochemical impedance spectroscopy (EIS) and
potentiodynamic polarization methods. The CS surface morphology was
investigated by SEM. The obtained results showed that the prepared nonionic
surfactants are excellent inhibitor in 1 M HCl, and the inhibition efficiency (η)
increases with the inhibitor concentration and temperature increasing. The
adsorption of inhibitors on the CS surface obeys the Langmuir adsorption
isotherm equation. Thermodynamic parameters have been obtained by
adsorption theory. Polarization curves show that the synthesized inhibitors are
mixed-type inhibitors in hydrochloric acid.

The influence of the concentration of adenine (AD), as a safe inhibitor,

on the corrosion of low carbon steel (LCS) in aerated 4.0 M H2SO4 solutions
was studied [50]. The investigations involved weight loss, potentiodynamic
polarization, impedance and electrochemical frequency modulation (EFM)
methods. Variations of open-circuit potential (OCP) as a function of time till
steady-state potentials were also studied. Measurements were conducted under
the influence of various experimental conditions complemented with ex situ
EDX examinations of the electrode surface. By using EFM measurements,
corrosion current density was determined without prior knowledge of Tafel
slopes. Results obtained revealed that together with iodide ion, AD is an
effective corrosion inhibitor for LCS corrosion in H 2SO4 solutions. Synergism
between iodide ion and AD was proposed. Potentiodynamic polarization studies
showed that AD alone and the mixture of AD and iodide ions act as mixed-type
inhibitors for the corrosion of LCS in 4.0 M H2SO4 solution. The inhibition
mechanism involves the electrostatic adsorption of protonated AD molecules on

22
the LCS surface charged with a negative layer of chemisorbed I − ions. An
adherent layer of inhibitor is postulated to account for the protective effect. EDX
examinations of the electrode surface confirmed the existence of such adherent
layer on the electrode surface. The inhibition efficiency increases with increase
in the concentration of AD and immersion time. The potential of zero charge
(PZC) of the LCS electrode was determined in 4.0 M H2SO4 solutions in the
absence and presence of 0.001 M KI, and the mechanism of adsorption was
discussed. The results obtained from chemical and electrochemical
measurements were in good agreement.

The effect of some prepared compounds, namely thiazole derivatives on

the corrosion of C-steel in 2 M HCl solutions has been studied [51] using the
weight loss and electrochemical polarization methods. The results showed that
the inhibition efficiency of the investigated compounds was found to depend on
the concentration and the nature of the inhibitor. The presence of the substituted
donating group (–OCH3) plays an important role in the inhibition percentage of
these investigated compounds. The effect of temperature on the corrosion
behavior of C-steel in 2 M HCl without and with the inhibitors was studied in
the temperature range from 30 to 50°C. The activation and thermodynamic
parameters Ea , ΔH and ΔS were calculated. The inhibitors were adsorbed on
the C-steel surface according to Frumkin's adsorption isotherm. The synergistic
effect of some cations (Cu2+, Ni2+, Co2+ and Ca2+) on the corrosion inhibition of
C-steel in 2 M HCl in the presence and absence of the investigated compounds
was also studied by the weight loss method.

The inhibitive action of the aqueous extract of the root of shirsh el

zallouh (Ferula harmonis) toward the corrosion of C-steel in HCl solution was
investigated [52]. The inhibition efficiency was measured using weight loss and
potentiostatic polarization techniques. The electrochemical behavior of the
extract was investigated using cyclic voltammetry. It was found that the addition
of the extract reduces the corrosion rate of C-steel. The inhibition efficiency
increases with increasing extract concentration. The inhibitive effect of the
tested extract was discussed in view of adsorption of its components on the steel
surface. The adsorption of the extract components on the C-steel surface follows
Langmuir adsorption isotherm. The inhibition efficiency decreases as the
temperature is increased. The presence of extract increases the activation energy
of the corrosion process of C-steel. The curves of cyclic voltammetry technique
showed that the adsorbed molecules reduce the charge density on the steel
surface.

23
 Potentiodynamic polarisation, electrochemical impedance spectroscopy
and weight loss studies were carried out [53] on the inhibition of carbon steel in
1 M hydrochloric acid solution by three bipyrazolic compounds. The examined
inhibitors are 5,5′-dipropyl-1H,1′H-[3,3′]bipyrazolyl (Bp1), 5,5′-diphenyl-
1H,1′H-[3,3′]bipyrazolyl (Bp2) and 5,5′-bis-(4-chloro-phenyl)-1H,1′H-
[3,3′]bipyrazolyl (Bp3). All measurements show that inhibition efficiency
increases with increase in inhibitor concentration and the variation in inhibitive
efficiency mainly depends on the type and nature of the substituents present in
the inhibitor molecule to attain 98% for chloro derivative (Bp3) at 10 −3 M. This
reveals that inhibitive actions of bipyrazolic compounds were mainly due to
adsorption on steel surface. Adsorption of these inhibitors follows Langmuir
adsorption isotherm. Electrochemical impedance spectroscopy (EIS)
measurements showed that the dissolution process of steel occurred under
activation control. The curves of polarisation indicated that the examined
inhibitors act primarily as cathodic inhibitors. From the adsorption isotherm,
thermodynamic data for the adsorption process (K, ) are calculated and
discussed. Some quantum parameters (highest occupied molecular orbital
(HOMO) energy, lowest unoccupied molecular orbital (LUMO) energy and total
partial charge of inhibitors atoms) are computed.

In this work, the corrosion inhibition property and the antibacterial

activity of the aminotris-(methylenephosphonic) acid (ATMP) have been studied
[54]. ATMP has been evaluated as a corrosion inhibitor for carbon steel in 1 M
HCl solution using weight loss, potentiodynamic polarization and
electrochemical impedance spectroscopy (EIS) techniques. According to the
experimental results, the inhibition efficiency increased with increasing inhibitor
concentration. Tafel polarization study showed that the ATMP acts as a mixed
inhibitor. Data, obtained from EIS measurements, were analyzed to model the
corrosion inhibition process through appropriate equivalent circuit models.
Adsorption of ATMP on the carbon steel surface obeyed the Langmuir
adsorption isotherm. The calculated ΔGads value showed that the corrosion
inhibition of the carbon steel in 1 M HCl is mainly controlled by a physisorption
process. In addition, the effect of immersion time on the corrosion of carbon
steel was also studied in this work using ac impedance technique. The corrosion
inhibition mechanism of ATMP was discussed. This inhibitor can be also used
as biocide in aqueous environments. Our results showed that ATMP have an
antibacterial effect against both Gram positive and Gram negative bacteria. The
lowest MIC (0.2 mg l−1) was measured for Pseudomonas fluorescens while the
highest MIC was measured for Escherichia coli (3.1 mg l−1). In addition, the
results showed that the MIC of ATMP against Listeria innocua in a buffered
medium (pH 6.5) was of ca. 4-fold higher than MIC measured in unbuffered

24
medium. Thus, our findings showed that the antibacterial activity of ATMP is a
result of a combined effect of the pH solution and the chemical nature of the
used phosphonate molecule.

In this investigation [55], attempts have been made to study the

inhibitive effect of N,N′-ortho-phenylen acetyle acetone imine (S1) and 4-[(3-
{[1-(2-hydroxy phenyl) methylidene] amino} propyl) ethanemidol]-1,3-
benzenediol (S2) in the concentration range of 50–400 ppm for mild steel with
two different microstructures resulted from two different heat treatments
(annealed (A) and quenched and tempered (Q&T)) in 1 M hydrochloric acid
solution. Both Schiff bases acted as a mixed type inhibitors. The S1 inhibitor for
both microstructures showed better inhibition efficiency than S2. The A samples
indicated slightly less corrosion than Q&T samples in 1 M HCl solution in
absence of inhibitor due to the formation of duplex γ-Fe2O3/Fe3O4.

The efficiency of three furan derivatives (2-methylfuran, furfuryl

alcohol and furfurylamine), as corrosion inhibitors for carbon steel in 1 M HCl,
has been determined [56] by gravimetric and electrochemical measurements.
These compounds inhibit corrosion even at very low concentrations, and
furfuryl alcohol is the best inhibitor. Polarization curves indicate that all
compounds are mixed inhibitors, affecting both cathodic and anodic corrosion
currents. Adsorption of furan derivatives on the carbon steel surface is in
agreement with the Langmuir adsorption isotherm model, and the calculated
Gibbs free energy values confirm the chemical nature of the adsorption. The
structural and electronic properties of these inhibitors, obtained using AM1,
PM3, MNDO and MINDO/3 semi-empirical self-consistence field methods, are
correlated with their experimental efficiencies.

A triazole-based cationic gemini surfactant, 3,5-bis(methylene octadecyl

dimethylammonium chloride)-1,2,4-triazole (18-triazole-18) has been
synthesized, and its effect on corrosion inhibition of A 3 steel in 1 M HCl has
been studied [57] using the weight-loss method. The result showed that 18-
triazole-18 acted as an excellent inhibitor in 1 M HCl. It was found that the
adsorption mechanism of 18-triazole-18 on the steel surface in acid medium was
quite different from that of cationic gemini surfactants containing dimethylene
as a spacer, as well as that of conventional cationic single-chained surfactants,
which is due to unique molecular structure of 18-triazole-18. 18-Triazole-18
may be adsorbed on the steel surface in acid medium through a maximum of
four atoms or groups, i.e., the two nitrogen atoms of triazole ring and two
quaternary ammonium head groups. Four regions of surfactant concentration
could be divided to illustrate the adsorption of 18-triazole-18 on the steel

25
surface, and four different adsorption mechanisms may take place in different
regions of surfactant concentration.

The effect of ammonium polymolybdate (APM) on the corrosion of

carbon steel in a solution of 1 M HCl was studied [58] by weight loss and
Mössbauer spectrometry. Inhibition efficiencies (P) have been obtained from
weight measurement. The inhibition efficiencies increased with increase APM
concentration. Mössbauer spectrometry shows that a superficial compound is
formed on the electrode surface as a result of corrosion.

The effect of succinic acid (SA) on the corrosion inhibition of a low

carbon steel (LCS) electrode has been investigated [59] in aerated non-stirred
1.0 M HCl solutions in the pH range (2–8) at 25 °C. Weight loss,
potentiodynamic polarization and electrochemical impedance spectroscopy
(EIS) techniques were applied to study the metal corrosion behaviour in the
absence and presence of different concentrations of SA under the influence of
various experimental conditions. Measurements of open circuit potential (OCP)
as a function of time till steady-state potentials (Est) were also established.
Surface analysis using energy dispersive X-ray (EDX) and scanning electron
microscope (SEM) allowed us to clarify the mechanistic aspects and evaluate
the relative inhibition efficiency. Results obtained showed that SA is a good
―green‖ inhibitor for LCS in HCl solutions. The polarization curves showed that
SA behaves mainly as an anodic-type inhibitor. EDX and SEM observations of
the electrode surface confirmed existence of a protective adsorbed film of the
inhibitor on the electrode surface. The inhibition efficiency increases with
increase in SA concentration, pH of solution and time of immersion. Maximum
inhibition efficiency (≈97.5%) is obtained at SA concentrations >0.01 M at pH
8. The effect of SA concentration and pH on the potential of zero charge (PZC)
of the LCS electrode in 1.0 M HCl solutions has been studied and the
mechanism of adsorption is discussed. Results obtained from weight loss,
polarization and impedance measurements are in good agreements.

The inhibiting effect of 12-aminododecanoic acid (AA) on corrosion of

carbon steel (CS) in CO2-saturated hydrochloric acid was investigated [60]. It
was found that AA acts as a mixed-type inhibitor, yielding a maximum
inhibition efficiency of 98.1 ± 0.1%. The mechanism of its corrosion inhibition
is by formation of a self-assembled monolayer (SAM), which presents a tight
hydrophobic barrier imposed by the (–CH2)11 chain. In-situ PM-IRRAS
measurements revealed that the SAM is amorphous. The SAM formation
process was found to be spontaneous and reversible. The corresponding standard
Gibbs energy of AA adsorption on CS was calculated to be −28 kJ mol−1.

26
 The conductivity, weight loss and A.C. impedance studies were carried
out [61] to establish the influence the presence of neutral copolymer (Vinyl
pyrrodlidone/Vinyl acetate copolymer) with anionic surfactant (Disodium
laurethsulfosuccinate) in cyclohexane propionic acid (CHPA) on the corrosion
behaviour of carbon steel. The protection efficiency (P%) of AS in the absence
and presence of polymer increases with increase in AS concentration until it
reaches a maximum constant value near the CMC of AS and decreases with
increase in solution temperature. The protective efficiency of AS can be
enhanced and its critical micelle concentration shifts to low value by adding of
0.05 g/l of polymer. The critical micelle concentration of AS in the absence and
presence of polymer increases with increase in temperature. The calculated
thermodynamic parameters of micellization (ΔGmic), (ΔHmic) and (ΔSmic) in the
presence of neutral copolymer molecules with AS show that these processes are
spontaneous and exothermic in nature and indicate the association between AS
and neutral copolymer molecules.

Ohmic drop corrected steady-state current—voltage curves and

electrochemical impedance diagrams have been obtained [62] for carbon steel
rotating disc electrodes in 200 mg l −1 NaCl solutions with and without addition
of 1 g l−1 of the association of oleylamino propylene and amino-tri[methyl-
phosphonic] acid (FA + TMPA). Corrosion rates determined from both steady
state and impedance data are in fairly good agreement with those determined
from gravimetric measurements carried out on a semi-pilot scale circuit.
Because impedance measurements are non-destructive and not affected by low
electrolyte conductivity, they allow us to follow the evolution of the corrosion
rate as a function of time: in the absence of inhibitor the corrosion rate increases
during the early stages of immersion whereas it decreases in the presence of 1 g
l−1 (FA + TMPA). Impedance diagrams obtained in inhibited solutions reveal a
high frequency loop unobserved in the absence of the inhibitor; the very low
value (1–2 μF cm−2) of the capacity associated to this loop suggests that the
inhibitor (FA + TMPA) acts in forming a relatively thick and compact protective
film on the metal surface.

The inhibition effect of propargyltriphenylphosphonium bromide

(PgTPhPBr), with a structure (CH C–CH2–)(C6H5–)3 P+Br, on the
electrochemical and corrosion behavior of three 0.1, 0.5 and 1.0% C-steels and
pure iron in deaerated 1 M H2SO4 solution at different temperatures was studied
[63] using linear polarization resistance, polarization curves and SEM
investigations. It was found that 0.5% C-steel (CS2) has high density of active
sites on the surface leading to high corrosion rate. PgTPhPBr acted as a mixed

27
type inhibitor with anodic predominance in case of pure iron and a mixed type
inhibitor in case of C-steels. The inhibition efficiency of PgTPhPBr increased
with increasing temperature up to 60 °C. Adsorption of the inhibitor was found
to follow the Langmuir’s isotherm. This inhibitor was more efficient for CS2
than for other samples at different temperatures. It was proposed that PgTPhPBr
decreases the corrosion rate through the reduction mechanism of metal
reactivity.

The influence of thiosemicarbazide, phenylthiosemicarbazide Girad’s-T

and phenylthiosemicarbazide Girard’s-P on the corrosion rate of steel in 2 M
HCl has been studied [64]. The protection efficiency obtained by weight-loss
and potentiostatic polarisation techniques was found to be in good agreement
with adsorption measurements at Pt electrode. The behaviour was correlated to
the proposed skeletal representation of the adsorption mode of the inhibitors on
the metal surface. Electrochemical results indicated that all the compounds
investigated acted as cathodic-type inhibitors. The data obtained provide a good
fit to both the Temkin adsorption isotherm and the kinetic–thermodynamic
model recently proposed.

Weight loss studies showed [65] that both 2-mercaptothiazoline and

cetyl pyridinium chloride are effective for the inhibition of low carbon steel over
a wide concentration range of aqueous phosphoric acid solution. The results for
uninhibited acid confirm the kinetic expression proposed by Mathur and
Vasudevan (Corrosion 38 (1982) 171).

Corrosion inhibition of C-steel in 2 M HCl was investigated [66] in the

absence and presence of different concentrations of some thiosemicarbazide
derivatives namely, 1-ethyl-4(2,4-dinitrophenyl) thiosemicarbazide (I), 1,4-
diphenylthiosemicarbazide (II), 1-ethyl-4-phenylthiosemicarbazide (III). Weight
loss, potentiodynamic polarization and electrochemical impedance spectroscopy
techniques were employed. Impedance measurements showed that the double-
layer capacitance decreased and charge-transfer resistance increased with
increase in the inhibitors concentration and hence increasing in inhibition
efficiency. Potentiodynamic polarization study showed that all the inhibitors act
as mixed-type inhibitors. Results obtained reveal that the inhibition efficiency
(%IE) follows the sequence: I > II > III. The adsorption of these compounds on
C-steel surface obeys Temkin’s adsorption isotherm and has a chemisorptions
mechanism.

The inhibition effect of some PEGs on carbon steel corrosion at 25 °C in

0.5N hydrochloric acid as corroding solution was evaluated [67] by weight loss

28
method and polarization and electrochemical impedance spectroscopy (EIS)
techniques. In order to study the effect of polyethylene glycols’ structure on the
inhibition efficiency, different molecular weights (400, 1000, 4000, and
10,000 g mol−1) were selected. This work has demonstrated that polyethylene
glycols have inhibition effect on corrosion process and their inhibition
efficiencies are between 50 and 90%. The inhibition efficiencies are increased
by increase of the inhibitors’ concentration and molecular weight.

In this paper, the corrosion inhibition of cationic gemini surfactant, in

the absence and presence of halide salts (NaCl, NaBr and NaI) on steel in HCl
was investigated [68] at 20 ± 1 °C. The effects of pH, immersion time and salt
concentration on the corrosion inhibition of steel were studied using weight loss,
open circuit potential and electrochemical impedance spectroscopy. Inhibition
efficiency increases by increasing surfactant concentration. Synergistic effect
between surfactant and salts was studied. The inhibition efficiency increases by
increasing salt concentration. This composite inhibitor containing gemini
surfactant and halide was efficient and low-cost for steel corrosion inhibition in
HCl.
We report here the use of macrocyclic polyether compounds containing
a 1,3,4-thiadiazole moiety (n-MCTH) in the corrosion inhibition of C38 carbon

steel in 0.5 M H2SO4 acid medium.

The aim of this work is devoted to study [69] the inhibition characteristics of
these compounds for acid corrosion of C38 steel using electrochemical
impedance spectroscopy (EIS). Data obtained from EIS show a frequency
distribution and therefore a modeling element with frequency dispersion
behaviour, a constant phase element (CPE) has been used. The experimental
results obtained revealed that these compounds inhibited the steel corrosion in
acid solution and the protection efficiency increased with increasing inhibitors
concentration. The difference in their inhibitive action can be explained on the
basis of the number of oxygen atoms present in the polyether ring which
contribute to the chemisorption strength through the donor acceptor bond
between the non bonding electron pair and the vacant orbital of metal surface.
Adsorption of n-MCTH was found to follow the Langmuir’s adsorption
isotherm. The thermodynamic functions of adsorption process were calculated

29
and the interpretation of the results is given. These results are complemented
with quantum chemical study in order to provide an explanation of the
differences between the probed inhibitors. Correlation between the inhibition
efficiency and the structure of these compounds are presented.

The effect of some aminopyrimidine derivatives on the corrosion of

1018 carbon steel in 0.05 M HNO3 solution was studied [70] using weight loss
and polarization techniques. The percentage inhibition efficiency was found to
increase with increasing concentration of inhibitor and with decreasing
temperature. The addition of KI to aminopyrimidine derivatives enhanced the
inhibition efficiency due to synergistic effect. The inhibitors are adsorbed on the
steel surface according to Temkin isotherm. Some thermodynamic functions
were computed and discussed. It was found that the aminopyrimidine
derivatives provide a good protection to steel against pitting corrosion in
chloride containing solutions.

The inhibitive action of the aqueous extracts of fruit peels against

corrosion of carbon steel in a 1 M HCl solution was investigated [71] using
electrochemical impedance spectroscopy, potentiodynamic polarization curves,
weight loss measurements and surface analysis. We analyzed aqueous extracts
of mango, orange, passion fruit and cashew peels in different concentrations and
found that the extracts act as good corrosion inhibitors for the tested system. The
inhibition efficiency increases with increasing extract concentration and
decreases with temperature. The adsorption of components of the fruit peel
extracts on the surface of the carbon steel follows the Langmuir adsorption
isotherm.

The inhibiting action of some polyethylene glycols on carbon steel

corrosion, using 3N sulphuric acid as corroding solution, was evaluated [72] by
the weight loss method and polarization and impedance spectroscopy
techniques. In order to study the effect of polyethylene glycol structure on the
inhibition efficiency, different molar weights (200–10,000 g mol−1) were
selected. This work has demonstrated that the polyethylene glycols have an
inhibition effect on the corrosion process and the inhibition efficiency is more
than 90%. It was shown that polyethylene glycol is adsorbed physically on
carbon steel in acid medium.

Electrochemical techniques have been used for investigating [73] the

inhibition of carbon steel by thiomorpholin-4-ylmethyl-phosphonic acid
(TMPA) and morpholin-4-methyl-phosphonic acid (MPA) in natural seawater.
The free corrosion potential was observed to the shift in noble direction which

30
indicated that the phosphonic acids tested inhibit the corrosion of carbon steel in
seawater. Potentiodynamic polarization curve shows clearly the fact that the
addition of these molecules is associated with corrosion current density decrease
and a corresponding reduction of the corrosion rate. The phosphonic acids tested
as corrosion inhibitors of carbon steel in natural seawater are effective even with
small concentration. Fourier transform infrared spectroscopy was used to obtain
information on bonding mechanism between the metallic surface and the
inhibitors. The morphology of the metal surface in the uninhibited and inhibited
solution was examined using the scanning electron microscope coupled with an
energy dispersive X-ray analysis system.

The corrosion inhibition characteristics of the synthesized cationic

Gemini surfactants, namely bis(p-(N,N,N-decyldimethylammonium
bromide)benzylidene thiourea (10-S-10), bis(p-(N,N,N-
dodecyldimethylammonium bromide)benzylidene thiourea (12-S-12) and bis(p-
(N,N,N-tetradecyldimethylammonium bromide)benzylidene thiourea (14-S-14)
on the carbon steel corrosion in 1 M hydrochloric acid have been investigated
[74] at 25 °C by weight loss, potentiodynamic polarization and electrochemical
impedance spectroscopy (EIS) techniques. The inhibition efficiencies obtained
from all methods employed are in good agreement with each other. The obtained
results show that compound 14-S-14 is the best inhibitor with an efficiency of
97.75% at 5 × 10−3 M additive concentration. Generally, the inhibition
efficiency increased with increase of the inhibitor concentration. Changes in
impedance parameters (charge transfer resistance, Rct, and double-layer
capacitance, Cdl) were indicative of adsorption of 14-S-14 on the metal surface,
leading to the formation of a protective film. The potentiodynamic polarization
measurements indicated that the inhibitors are of mixed type. The adsorption of
the inhibitors on the carbon steel surface in the acid solution was found to obey
Langmuir’s adsorption isotherm. The free energy of adsorption processes were
calculated and discussed. The surface parameters of each synthesized surfactant
were calculated from its surface tension including the critical micelle
concentration (CMC), maximum surface excess (Γmax) and the minimum surface
area (Amin). The free energies of micellization (ΔGomic) were calculated. The
surface morphology of carbon steel sample was investigated by scanning
electron microscopy (SEM).

The corrosion inhibition of carbon steel in HCl and H2SO4 solutions in

the presence of some benzimidazole derivatives such as benzimidazole (BI), 2-
methylbenzimidazole (2-CH3-BI) and 2-mercaptobenzimidazole (2-SH-BI) was
investigated [75] using potentiodynamic polarization technique. Results
obtained showed that the benzimidazole derivatives retard both the cathodic and

31
anodic reactions in both acidic media, by virtue of adsorption on the carbon steel
surface. This adsorption obeyed Langmuir's adsorption isotherm. In the both
media, 2-SH-BI showed the highest efficiency while the lowest efficiency was
observed for BI. The comparative analysis of the inhibitor adsorption in both the
media, as well as, the synergistic effect of bromide ions (Br −) in H2SO4 solution
suggests that the physical adsorption of the cationic form of BI and 2-CH3-BI
occurs, while 2-SH-BI is adsorbed chemically.

The influence of cetyl trimethyl ammonium bromide (CTAB) on the

corrosion of carbon steel in HCl and H2SO4 solutions has been studied [76]
using several techniques such as weight loss, Tafel polarization, linear
polarization and open circuit potential. Inhibition efficiencies have been
obtaining from weight loss measurement, the effect of temperature on corrosion
inhibition and the effectiveness of the inhibitor at higher acid strength have been
examined. Polarization studies reveal that the inhibitor behaves as an effective
inhibitor in H2SO4 as well as in HCl solutions. Measurements of values of
polarization resistance (Rp) have also been carried out. The open circuit potential
curves was shifted to less negative potential contrary to the blank.

The effect of chloride and nitrite ions on the passivity of steel in alkaline
solutions was investigated [77]. Four nitrite dosages were tested, resulting in
various nitrite/chloride ratios. The behavior of steel was evaluated on electrodes
aged during 1 and 90 days, measuring electrochemical parameters such as the
corrosion, pitting and repassivation potentials, the corrosion current density, the
weight loss and performing electrochemical impedance spectra. The presence of
0.8 mol l−1 of chloride induced pitting only under polarization and when the
chloride/hydroxyl ratio was not less than one. Nitrite ions behave as effective
inhibitors of pit propagation for all the concentrations tested (0.2–0.8 mol l−1). A
nitrite/chloride ratio of 0.25 induces complete surface repassivation.
Nevertheless, at open circuit potential, the high alkalinity guarantees passivation
even in the presence of chlorides. In the event that the passive layer is damaged
and pitting can be initiated, nitrite ions are effective in inhibiting pit
propagation.

The role of iron-reducing bacteria (IRB) in biocorrosion is under

discussion [78]. According to some reports, IRB are able to induce protection of
carbon steel while others suggest an important enhancement of corrosion
through the reduction and removal of passive films of ferric compounds on the
metal surface. In this work, we review recent knowledge concerning microbial
respiration, the ecology of IRB containing biofilms and the corrosive or
protective effect of such biofilms on metal surfaces.

32
 The effect of pH value on the adsorption behavior and inhibition
mechanism of dodecylamine for carbon dioxide corrosion of carbon steel was
investigated [79] by electrochemical methods and scanning electron microscopy
(SEM). The results indicated that the pH value of the solution played the crucial
role to the adsorption behavior and inhibition mechanism of dodecylamine. The
inhibition performance of dodecylamine on carbon steel was dependent on the
pH value and the inhibition efficiency increased with the increase of pH value.
At pH 4.9, dodecylamine mainly inhibited the cathode process of the corrosion.
The adsorption energy of dodecylamine on the metal surface was lower. The
adsorption of dodecylamine on the metal surface was not stable and an anode
desorption phenomenon could be observed. Hence, dodecylamine did not
provide effective inhibition to the corrosion. While at pH 6.9, it had much higher
adsorption energy. Dodecylamine adsorbed on the metal surface tightly and
formed the effective diffusion barrier which inhibited both the cathode and
anode processes effectively.

The role of acetic acid (HAc) on the pit growth in CO 2 corrosion of

carbon steel pipelines is studied [80] by means of an artificial pit electrode. The
current flowing between the artificial pit and the outer surface was measured
with a zero resistance ammeter. It is shown that the corrosion potential increases
with increasing HAc concentration. Depletion of HAc inside the pit imposed a
potential difference that triggered the pit growth. The pit did not grow in
absence of HAc. The pit growth was self-sustained only to a certain pit depth,
beyond which the dissolution current at the bottom of the pit vanished. This is in
good agreement with field observations mainly in the case of top-of-line
corrosion phenomena.

The role of water, acetic acid, chloride, and oxygen level in corrosion
and pitting behaviour of carbon steel in simulated fuel-grade ethanol (SFGE)
was investigated [81]. In the absence of the supporting electrolyte, modified cell
geometry enabled us to conduct the electrochemical measurement in low-
conductivity ethanolic solutions. Results have shown that the water in the SFGE
strongly influences the surface film stability and interface electrochemistry in
ethanolic environments. The increase in the water concentration induces pitting
and metal loss. Dissolved chlorides and higher acidity promote the pit initiation
and growth. Alkaline condition inhibits both localized and uniform corrosion.

Four Gemini surfactants were synthesized and characterized using

elemental analysis, FTIR and 1H NMR spectroscopy. The synthesized
compounds were evaluated [82] as corrosion inhibitors for carbon steel in 0.5 M

33
HCl solution. The inhibition efficiencies of the tested inhibitors were depended
on the hydrophobic chain length and the used doses of the inhibitors. The
polarization measurements showed that these inhibitors are acting as mixed
inhibitors for both anodic and cathodic reactions. The results showed that the
inhibition efficiencies were increased by increasing the inhibitor doses and the
hydrophobic chain length and reached the maximum at 500 ppm by weight for
stearyl derivative. The efficiencies obtained from the impedance measurements
were in good agreement with those obtained from the gravimetrical and
polarization techniques which prove the validity of these tolls in the
measurements of the tested inhibitors.

Potentiodynamic polarisation and ac impedance studies were carried out

[83] on the inhibition of carbon steel in 0.1 M hydrochloric acid solution by
various Schiff bases containing heteroaromatic substituents. The examined
Schiff bases were 2-((1E)-2-aza-2-pyrimidine-2-ylvinyl)thiophene, 2-((1Z)-1-
aza-2-(2-pyridyl)vinyl)pyrimidine, 2-((1E)-2-aza-2-(1,3-thiazol-2-
yl)vinyl)thiophene, 2-((1Z)-1-aza-2-(2-thienyl)vinyl)benzothiazole. Polarisation
curves indicates that studied Schiff bases act essentially as anodic inhibitor. The
variation in inhibitive efficiency mainly depends on the type and nature of the
substituents present in the inhibitor molecule. Potentiodynamic polarisation and
ac impedance measurements carried out at different concentration of studied
Schiff bases reveal that these compounds are adsorbed on steel surface and the
adsorption obeys Temkin’s adsorption isotherm. From the adsorption isotherms
values of equilibrium constant, Kads, values of free energies of adsorption, ΔGads,
were calculated. Activation parameters of the corrosion process such as
activation energies, Ea, activation enthalpies, ΔH*, and activation entropies, ΔS*,
were calculated from the obtained corrosion rates at different temperatures.

Cold plasma nitriding treatment was performed [84] to improve the

corrosion resistance of C38 carbon steel. Nitriding process was conducted using
a radiofrequency nitrogen plasma discharge for different times of treatment on
non-heated substrates. The modification of the corrosion resistance
characteristic of the C38 steel due to the treatment in acid medium (1 M HCl)
were investigated by gravimetric and electrochemical tests such as
potentiodynamic polarisation curves and electrochemical impedance
spectroscopy (EIS). It was shown that the plasma nitriding treatment improves
the corrosion resistance. Indeed, in the gravimetric tests, nitrided samples
showed lower weight loss and lower corrosion rate in comparison to untreated
one. In the Tafel polarisation tests, the nitrided samples showed greatly reduced
corrosion current densities, anodic dissolution and also retarded the hydrogen
evolution reaction. Using EIS method, an adequate structural model of the

34
interface was used and the values of the corresponding parameters were
calculated and discussed. The results obtained from weight loss and
electrochemical studies were in reasonable agreement. X-ray photoelectron
spectroscopy (XPS) was carried out to establish the mechanism of corrosion
inhibition of nitrided C38 steel in 1 M HCl medium. The enhancement of the
corrosion resistance is believed to be related to the iron nitride compound layer
formed on the C38 steel surface during plasma nitriding, which protected the
underlying metal from corrosive attack in the aggressive solutions.

The effect of a new class of corrosion inhibitors, namely,

Arylazobenzoyl acetonitrile derivatives, on the corrosion of carbon steel in 2 M
HCl and 1 M H2SO4 solutions has been studied [85] by electrochemical
polarisation methods (potentiodynamic, Tafel extrapolation and the
determination of polarisation resistance). Generally, inhibition efficiency of the
investigated compounds was found to increases with increasing concentration.
Results obtained from both potentiodynamic and polarisation resistance
techniques reveal that these compounds are good inhibitors and behave better in
2 M HCl than 1 M H2SO4. The adsorption of the compounds on the carbon steel
in both acidic media follows a Langmuir adsorption isotherm.

The electrochemical behavior of SAE-1020 carbon steel in 0.25 M

Na2SO4 solution containing different concentrations of H2S at 90 °C was
investigated [86] using the methods of weight loss, electrochemical
measurements, scanning electron microscopy (SEM) and X-ray diffraction
(XRD). The results showed that the corrosion rate of carbon steel increased
significantly with the increase of H2S concentration. H2S accelerated the
corrosion rate of SAE-1020 carbon steel by a promoted hydrogen evolution
reaction. Severe corrosion cavities were observed on the carbon steel surface in
the solutions containing H2S due to cementites stripped off from the grain
boundary. The loose corrosion products formed on the steel surfaces were
composed of mackinawite.

The behavior of the Schiff base N,N′-bis(salicylidene)-1,2-

ethylenediamine (Salen), its reduced form (N,N′-bis(2-hydroxybenzyl)-1,2-
ethylenediamine) and a mixture of its preceding molecules, ethylenediamine and
salicylaldehyde, as carbon steel corrosion inhibitors in 1 mol L−1 HCl solution
was studied [87] by corrosion potential measurements, potentiodynamic
polarization curves, electrochemical impedance spectroscopy and
spectrophotometry measurements. The experimental results showed that the
reduced Salen presented the highest efficiency among the inhibitors studied. The
results obtained in the presence of Salen were similar to those obtained in the

35
presence of the salicylaldehyde and ethylenediamine mixture, showing that in
acid medium the Salen molecule undergoes hydrolysis, regenerating its
precursor molecules.

The efficiency of three furan derivatives (2-methylfuran, furfuryl

alcohol and furfurylamine), as corrosion inhibitors for carbon steel in 1 M HCl,
has been determined [88] by gravimetric and electrochemical measurements.
These compounds inhibit corrosion even at very low concentrations, and
furfuryl alcohol is the best inhibitor. Polarization curves indicate that all
compounds are mixed inhibitors, affecting both cathodic and anodic corrosion
currents. Adsorption of furan derivatives on the carbon steel surface is in
agreement with the Langmuir adsorption isotherm model, and the calculated
Gibbs free energy values confirm the chemical nature of the adsorption. The
structural and electronic properties of these inhibitors, obtained using AM1,
PM3, MNDO and MINDO/3 semi-empirical self-consistence field methods, are
correlated with their experimental efficiencies.

The inhibition effect of Ni2+ cation, 3-methyl pyrazolone (3-MP) and

mixture of them on the corrosion of carbon steel in 0.5 M H2SO4 solution was
studied [89] using weight loss, galvanostatic and potentiodynamic anodic
polarization techniques. The inhibition efficiency increases with increasing
concentration of Ni2+ and 3-MP. The mixtures of Ni2+ and 3-MP improved the
inhibition efficiency. The formation of complex compound was discussed
depending on the results derived from UV–visible spectrophotometric
measurements as well as conductometric titration.
The corrosion behaviour of carbon steel at six test sites in Colombia and
its relationship with exposure time and environmental characteristics of each site
were investigated [90]. The corrosion products were characterized by XRD,
SEM and EDS. It was found that in Barranquilla, the most aggressive site,
corrosion depends mainly on chlorides. Furthermore, in the more aggressive
environments there was a greater tendency to formation of protective corrosion
products. Lepidocrocite and goethite were found as major constituents of rust. A
structure not reported in the literature was found, corresponding to strings of
several hundred micrometers long and consisting of lepidocrocite plates.

The atmospheric corrosion kinetics of low carbon steel exposed for up to

36 months in marine and industrial sites was studied [91] by weight loss
measurements. The results show that the mechanism and kinetics of the
atmospheric corrosion process presents transition behaviour in marine
environments with high chloride ion content and high relative humidity, whereas
no transition appears in industrial environment. The average corrosion velocity

36
in marine site reaches a maximum during the period of transition and then
fluctuates in a certain range; however, the instantaneous corrosion velocity
follows different exponential functions before and after the period of transition.

37
The present work was designed to:
1. Investigate the inhibiting effect of some inhibitors towards the corrosion of
C- steel in 1 M HCl.

2. Determine the rate of corrosion of the C- steel, in the presence and absence
of these derivatives by weight- loss method (chemical method), and DC, AC
(electrochemical methods).

3. Study the effect of the temperature on the corrosion rate by one of the two
methods this enable us to:
(a) Calculate the thermodynamic parameters related to the corrosion process.
(b) Determine the kind of adsorption isotherm and the type of noidprosda
(physical or chemical).

4. Investigate the synergistic effect of potassium iodide, potassium thiocyanate

and potassium bromide on the corrosion inhibition in presence of these
investigated additives.

5. Determine the mechanism and percentage inhibition of these additives.

6. Calculate some quantum-chemical parameters and relate it to the inhibition

efficiency.

7. Finally, order these additives according to their percentage inhibition.

38