Wet Corrosion

Wet Corrosion
Corrosion is defined as the deterioration of a material by chemical or electro chemical

reactions with its environment. Due to corrosion the useful properties of a metal like
malleability, ductility, electrical conductivity and also the surface appearance are
compromised. The most familiar example of corrosion is the rusting of iron when exposed
to atmospheric conditions.
There are several types of corrosion, including wet corrosion and dry corrosion.
Dry corrosion occurs when there is no water or moisture to aid the corrosive process, and
the metal oxidizes with the atmosphere alone. Wet corrosion of metals occurs through
electron transfer, involving two processes, oxidation and reduction. In oxidation, the metal
atoms lose electrons. The surrounding environment then gains the electrons in reduction.
The metal, where electrons are lost, is called the anode. The other metal, liquid or gas
which gains the electrons is called the cathode.
Air contains, on average, 21% oxygen, 78% nitrogen, and 1% argon. It can also contain
water vapour, ozone, and carbon dioxide.
Water is very commonly aerated which again means there is oxygen available for reaction
with metals.
There are many factors that dictate how corrosive an environment is. One is the amount of
oxygen available to form corrosion products or the presence of water or moisture which
greatly accelerate the rate of corrosion. Another is the presence of other elements, ions and
compounds that can limit or enhance corrosion rates. Therefore corrosion rates are often
considered in different atmospheres: industrial, rural and marine. Each of these
environments will contain different amounts of oxygen and other “pollutants” like ozone,
salt, dusts, sulphur dioxide, ammonia, hydrogen and hydrogen sulphide.
Figure 1: Types of corrosion

Electrochemical theory of wet corrosion: fundamentals
As with dry corrosion wet corrosion reactions are only possible if the free energy of the
products of reaction is lower than the free energy of the reactants. This is the case however
for the reaction of nearly all metals with water and oxygen to give metal hydroxides:
M + H2O (l) → M(OH)2 (s) … (1)
This enables reaction 1 above to proceed through the coupling of two primary corrosion
reactions:
A: M→M2+ + 2e‾ … (2)
(Anode reaction: destroys metal, releases electrons, oxidation)
C: 2e‾ + H2O + ½O2 → _2OH … (3)
(Cathode reaction: consumes electrons; electron sink reaction: reduction).
Electrons liberated in the anode reaction A flow to the site of the cathode
reaction C through the conducting metal. The movement of dissociated ions carries an
equal ionic current in the water. The distances over which these currents flow can vary
from microns to many metres. All wet corrosion processes can be analysed in terms of
anodic and cathodic reactions.
The anodic process is the direct cause of damage to metallic structures but both an anodic
and a cathodic process must occur for a corrosion cell to be formed. The corrosion of
metals by reaction with air and water to form metal hydroxides as shown above is a very
important wet corrosion process, especially in the construction industries. There are other
corrosion reactions resulting from, for example, other cathode reactions (electron-
consuming).
The rate of wet corrosion may often be very high compared with dry corrosion on the same
metal at the same temperature. There are two underlying reasons for this:
- the dipolar water molecule stabilizes the free (dissociated) metal ions in solution
- the metallic structure and water in contact with it can both conduct electric current
This enables reaction 1 above to proceed through the coupling of two primary corrosion
reactions:
All wet corrosion processes can be analysed in terms of anodic and cathodic reactions.
The anodic process is the direct cause of damage to metallic structures but both an anodic
and a cathodic process must occur for a corrosion cell to be formed
The corrosion of metals by reaction with air and water to form metal hydroxides as shown
above is a very important wet corrosion process, especially in the construction industries.
There are other corrosion reactions resulting from, for example, other cathode reactions
(electron-consuming)
2e‾ + 2H+ → H2 … (4)
2e‾ + M2+ → M2+ … (5)
or other anode reactions (electron releasing)
M + H2O →MO + 2H+ 2e‾ … (6)
When a metal M is placed in pure water, some ions will immediately pass into solution:
M→M2+ + 2e‾ … (7)
The build-up of negative charge on the metal and the build-up of metal ions in solution
makes possible a back-reaction:
M←M2+ + 2e‾ … (8)
and ultimately an equilibrium is established:
M↔_M2+ + 2e‾ … (9)
At this stage, a steady potential difference now exists between metal and solution. The
magnitude of this potential difference depends on the metal and composition of the
solution. It is not possible to measure this potential difference for a single metal, but the
potential difference (emf) between two metals dipping into a solution can be measured.
Under well-defined conditions, this enables a single potential Em (relative to a common
reference) to be assigned to every metal.

Wet Corrosion

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Wet Corrosion

Corrosion is defined as the deterioration of a material by chemical or electro chemical

Figure 1: Types of corrosion

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