GALVANIC OR TWO-METAL CORROSION

To understand corrosion forms and its evolution, it is necessary to be familiar to galvanic

effect beside what we learn about electrochemistry and metallurgy.
A potential difference usually exists between two dissimilar metals when they are immersed in
a corrosive or conductive solution. If these metals are placed in contact (or otherwise
electrically connected), this potential difference produces electron flow between them.
Corrosion of the less corrosion-resistant metal is usually increased and attack of the more
resistant material is decreased, as compared with the behavior of these metals when they are
not in contact.

Electromotive Force EMF and Galvanic Series

The potential between metals exposed to solutions containing approximately one gram atomic
weight of their respective ions (unit activity) are precisely measured at a constant temperature.
Table 3-1 presents such a tabulation, often termed the electromotive force or emf series. For
simplicity, all potentials are referenced against the hydrogen electrode (H2/H+) which is
arbitrarily defined as zero.
The amount of energy stored in the metal is known as the metal’s potential.
Different metals require different amounts of energy to refine and therefore have different
tendencies to corrode.
The greater the amount of energy required to refine a metal, the greater the tendency to corrode.
For example, iron has a much greater tendency to corrode than gold.
In actual corrosion problems, galvanic coupling between metals in equilibrium with their ions
rarely occurs. As noted above, most galvanic corrosion effects result from the electrical
connection of two corroding metals. Also, since most engineering materials are alloys, galvanic
couples usually include one (or two) metallic alloys.
Example 1

Half-Cell Potential for Copper

Suppose 1 g of copper as Cu2+ is dissolved in 1000 g of water to produce an electrolyte.

Calculate the electrode potential of the copper half-cell in this electrolyte.

SOLUTION

From chemistry, we know that a standard 1-M solution of Cu2+ is obtained when we add 1
mol of Cu2+ (an amount equal to the atomic mass of copper) to 1000 g of water. The atomic
mass of copper is 63.54 g/mol. The concentration of the solution when only 1 g of copper is
added must be:

Example.2

Design of a Copper Plating Process

Design a process to electroplate a 0.1-cm-thick layer of copper onto a 1 cm  1 cm cathode
surface.

SOLUTION Example 2

In order for us to produce a 0.1-cm-thick layer on a 1 cm2 surface area, the weight of
copper must be:

Example 3 Corrosion of Iron

An iron container 10 cm  10 cm at its base is filled to a height of 20 cm with a corrosive

liquid. A current is produced as a result of an electrolytic cell, and after 4 weeks, the
container has decreased in weight by 70 g. Calculate (1) the current and (2) the current
density involved in the corrosion of the iron.

Example 3 SOLUTION
1. The total exposure time is:

2. The total surface area of iron in contact with the corrosive liquid and the current density
are:

Example 4 Copper-Zinc Corrosion Cell

Suppose that in a corrosion cell composed of copper and zinc, the current density at the
copper cathode is 0.05 A/cm2. The area of both the copper and zinc electrodes is 100 cm2.
Calculate (1) the corrosion current, (2) the current density at the zinc anode, and (3) the
zinc loss per hour.

Example 4: SOLUTION

1. The corrosion current is:

2. The current in the cell is the same everywhere. Thus:

3. The atomic mass of zinc is 65.38 g/mol. From Faraday’s equation:

 Distance Effect
Accelerated corrosion due to galvanic effects is usually greatest near the junction, with attack
decreasing with increasing distance from that point.

Area Effect
Another important factor in galvanic corrosion is the area effect, or the ratio of the cathodic
to anodic areas. An unfavorable area ratio consists of a large cathode and a small anode. For
a given current flow in the cell, the current density is greater for a small electrode than for a
larger one, the greater the current density at an anodic area the greater the corrosion rate.
Corrosion of the anodic area may be 100 or 1000 times greatest than if the anodic and
cathodic areas were equal in size.