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Bimetallic Corrosion Basics PDF
Bimetallic Corrosion Basics PDF
CORROSION
BASICS
Bimetallic corrosion, as its name suggests, is corrosion that occurs due to the direct or indi-
rect contact between two metals. These metals, called coupling metals, are usually different
in property and composition. This type of corrosion can be observed in a number of different
environments. Rivets and bolts connecting metal components, an aluminum head on a cast
iron block, solder on a copper pipe, steel nails on Aluzinc sheeting, and flanges of connect-
ing metal pipes are all examples of everyday situations where bimetallic corrosion may be
found.
Although this type of corrosion may sound detrimental at first (and it usually is), there are
instances where this naturally occurring process is encouraged and used in a number of
beneficial applications.
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To understand how bimetallic corrosion works, it is beneficial to first understand the galvan-
ic series. When a metal is immersed in an electrolyte, it adopts an electrode potential that
represents the amount of energy that is available to drive the oxidation and reduction reac-
tions. The electrode potentials of various metals and alloys are calibrated and arranged in a
table or list that is referred to as the galvanic series. Metals and alloys positioned higher on
the list are referred to as anodic (more electronegative) while those listed lower on the list
are cathodic (more electropositive). (Learn more in An Introduction to the Galvanic Series:
Galvanic Compatibility and Corrosion.)
The main component that makes this type of corrosion possible is the difference in elec-
trode potentials that exists between two dissimilar metals when they are in contact with an
electrolyte. This entire system is known as a bimetallic couple, where one metal acts as the
anode and the other acts as the cathode.
The potential difference that is formed between the two dissimilar metals gives rise to a
flow of electrons from the electronegative anode to the more electropositive cathode; this
flow generates an electric current.
The resulting loss of electrons as they flow from the anode to the cathode triggers an ox-
idation reaction at the anode that causes it to corrode, while reduction takes place at the
cathode where dissolved oxygen is consumed, as illustrated by the two chemical reactions
shown in equations 1 and 2.
Fe → Fe2+ + 2e
Equation 1 – Typical oxidation of iron (e.g.) at the anode.
O2 + 2H2O + 4e → 4OH
Equation 2 – Typical reduction of dissolved oxygen at the cathode.
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Because the potential difference is directly related to the difference in reactivity between
the anode and the cathode, the further apart the two metals are in the galvanic series, the
greater the potential difference between the metals, and therefore the more severe the rate
of corrosion of the anode. In the same way, the closer the metals are in the series, the lower
the potential difference, therefore the lower the rate of corrosion. Hence, we can reason that
if the two contacting metals were the same then bimetallic corrosion would not occur.
ELECTROLYTE COMPOSITION
The pH of the electrolyte has also been known to affect the rate of bimetallic corrosion as
well. Advanced corrosion rates are known to occur as the pH drops below 4 for aluminum
and at about 6 for zinc and magnesium.
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ELECTRODE POTENTIAL
ELECTRODE EFFICIENCY
Galvanic corrosion is greatly affected by the ratio of the areas of the anode to the cathode.
The larger the area of the cathode relative to the anode, the greater the rate of oxygen re-
duction and the greater the galvanic current. Increased galvanic current results in the rapid
loss in thickness of the anode. The smaller the anode/cathode ratio, the less desirable the
situation becomes. For example, steel nails (anode) in a large copper plate (cathode) will
experience more aggressive corrosion than copper nails in a large steel plate.
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METALLURGICAL CONDITION AND COMPOSITION
Metallurgical composition can also cause changes in the electrode potential of a metal.
Quenching, tempering, annealing and other types of heat treatment can all affect the metal-
lurgical composition of a metal, which can cause potential differences between two similar
metals. Local changes in metal composition may also be brought on by heat-affected zones
(HAZ) in welding. For instance, austenitic stainless steel is more cathodic than martensitic
metals of the same type.
OBSTRUCTIONS
Uninterrupted cathodic reduction reactions must be sustained at the nobler of the two
metals for bimetallic corrosion to occur. In other words, dissolved oxygen from the electro-
lyte must be able to be consumed freely at the cathode without interference. The corrosion
products produced by some metals can form an effective oxide barrier that can prevent or
slow down oxidizers from reaching the metal’s surface, thereby stifling the corrosion pro-
cess. Bare metals, therefore, act as better cathodes than metals with oxide barriers because
these barriers impede oxygen diffusion to the cathode. In addition, oxide films also tend to
add additional resistance to the circuit that can slow down the electrochemical process even
further.
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ADVANTAGES OF BIMETALLIC
CORROSION
Bimetallic corrosion and its associated processes can be very damaging to metallic compo-
nents in contact with each other. However, there are a few instances where the processes
responsible for this natural phenomenon can be leveraged and used for positive applica-
tions. Listed below are some of the ways that bimetallic corrosion can be beneficial.
Bimetallic/galvanic corrosion is the driving force for producing electricity in galvanic cells
such as dry cell batteries. The flow of electricity (the movement of electrons from the anode
to the cathode) produces an electric current in the circuit, which gives batteries the ability to
produce various voltages. A typical dry cell battery consists of a zinc inner case (anode) and
a graphite rod within the case (cathode). To complete the circuit, an electrolyte, usually an
aluminum-based paste, bridges the two metals to facilitate the flow of electrons to produce
electricity.
CATHODIC/GALVANIC PROTECTION
The fact that one metal (the anode) corrodes preferentially with respect to the other (the
cathode) is used to purposely protect specific metal components. For example, zinc-based
coatings are commonly applied to structural steel members in a process known as galvaniz-
ing. The zinc offers cathodic protection to the steel by undergoing corrosion in the event that
the steel substrate becomes exposed. For example, if the steel substrate becomes exposed
by a scratch, this will trigger a galvanic cell that will cause the zinc coating around the
scratched surface to corrode while the steel substrate remains intact. This process contin-
ues until the zinc coating is fully depleted by the corrosion.
For larger structures, where passive galvanic methods are not sufficient, the metal to be
protected is connected to another sacrificial anodic metal via an external power source that
provides additional current to power the reaction. This is commonly used on long pipelines
and offshore oil and gas platforms.
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HOW TO MITIGATE AND PREVENT
BIMETALLIC CORROSION
There are several methods that are commonly used to prevent bimetallic corrosion. Most of
these solutions involve disrupting the electrical path between the anode and the cathode,
removing dissolved oxygen from the electrolyte or reducing the area ratio between the an-
ode and the cathode.
ELECTRICAL INSULATION
Insulation involves the use of non-conductive materials as a barrier between the contact
points of the coupling metals. By insulating or separating the direct contact of the coupling
metals, the flow of electrons from one metal to another is inhibited. In practical situations,
insulation materials may come in the form of rubber or polymer-based washers, gaskets,
coatings, etc.
ELECTROLYTE ISOLATION
Electrolyte isolation involves separating one or both of the metals from the medium that
facilitates the redox reactions in the galvanic cell. If the anode or cathode is unable to oxi-
dize or reduce, then the processes for bimetallic corrosion cannot happen. Water-repellent
compounds such as paints, greases and varnishes are just some of the methods used to
obscure contact between the electrolyte and the metals. These coatings have traditionally
been applied by electroplating, dipping or spraying.
CORROSION INHIBITORS
Corrosion inhibitors, usually liquid in nature, can be applied to the electrolyte to dampen the
corrosion processes occurring between the two metals. These inhibitors work in a variety
of ways, some involving complex chemical reactions. However, one of the most common
corrosion inhibitors used to combat bimetallic corrosion involves removing oxygen from the
electrolyte. Lack of dissolved oxygen content means little to no reduction can occur at the
cathode. Since reactions at the anode and cathode are dependent on each other, the entire
galvanic process comes to a halt.
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MAXIMIZING THE ANODE/CATHODE AREA RATIO
Making the area of the anode as large as possible in relation to the cathode can help to sig-
nificantly reduce (but not prevent) corrosion of the two metals. This can be achieved through
careful consideration and selection of the geometry and physical properties of the contacting
metals in the early stages of the design process. (For more on this subject, see Corrosion
Control Considerations in the Equipment Design Process.)
CONCLUSION
Bimetallic corrosion can cause accelerated corrosion in metals and can be found in a variety
of environments across a number of industries. However, this type of corrosion can be eas-
ily managed by the application of relatively inexpensive preventative measures. It is, there-
fore, important to understand the basic underlying principles behind bimetallic corrosion to
select the most effective solution for a given situation.
The same concept applies when using bimetallic corrosion for cathodic protection uses.
Proper anode and coating selection is crucial to the success of the chosen protection method.