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Materials for engineering, 3rd Edition - (Malestrom)

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Metals and alloys 125<br />

3.4.2 Corrosion of metals and alloys in aqueous<br />

environments<br />

Although we will use examples of metals being immersed in a liquid, the<br />

corrosion processes which occur are also encountered under conditions of<br />

ordinary atmospheric exposure, when the relative humidity is high.<br />

Condensation of moisture upon the metal surface then takes place and<br />

degradation by ‘wet corrosion’ is observed.<br />

It is well known that the mechanism of aqueous corrosion is electrochemical:<br />

a local anode is <strong>for</strong>med where the metal (M) enters solution:<br />

M → M 2+ + 2e [3.13]<br />

Electrons flow through the metal and are neutralized at a local cathode.<br />

There is a variety of possible reactions <strong>for</strong> this electron discharge and one of<br />

the most important, involving the absorption of oxygen, can be written as:<br />

O 2 + 2H 2 O + 4e → 4OH – [3.14]<br />

So OH – ions are produced in the liquid at the cathode, which thus becomes<br />

locally alkaline.<br />

Let us consider an iron specimen partially immersed in an electrolyte<br />

(Fig. 3.35). Atmospheric oxygen dissolves in the liquid, so the iron just<br />

beneath the surface of the liquid is surrounded by liquid with the highest<br />

dissolved oxygen content and, there<strong>for</strong>e, acts as a cathode. The bottom of the<br />

specimen, furthest removed from the surface, is surrounded by liquid with<br />

Iron<br />

Air<br />

Hydroxyl ions at cathode<br />

OH – OH – NaCl solution<br />

Electron flow<br />

e<br />

Ferrous ions at anode<br />

Fe 2+ Fe 2+<br />

3.35 A simple corrosion cell.<br />

Precipitate of rust away from<br />

both anode and cathode

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