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Alloy Corrosion

Published online by Cambridge University Press:  29 November 2013

R.C. Newman ,
S.G. Corcoran ,
J. Erlebacher ,
M.J. Aziz  and
K. Sieradzki
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Extract

The corrosion properties of alloys are of enormous practical importance: modern life would be very different without stainless steels. Alloy corrosion is also an intriguing field of scientific study that combines electrochemical kinetics with fashionable aspects of the morphological evolution of surfaces and even a dash of ancient history, via the studies of Forty and Lechtman on “depletion gilding” practiced by Early Andeans during pre-Columbian times in South America.

The basic alloy corrosion process, as used by the metalsmiths to gold-coat artifacts, is de-alloying. This is defined as the selective electrolytic dissolution of one or more components from a metallic solid solution. For this to happen, there must be a significant difference in the equilibrium metal/metal-ion electrode potentials for the two metals, taking into account any complex ions that might be formed in the electrolyte. For example, we can expect de-alloying in Au-Cu alloys, but not in Au-Pt alloys.

De-alloying shows sharp parting limits, expressed as critical atom percentages of the more reactive component above which that component can be removed from the alloy by electrochemical dissolution in an oxidizing environment such as nitric acid. Parting limits range from about 20 at.% to 60 at.%. This concept is still used in noble metal technology to separate noble metals from base metals. For example, an alloy of 55 at.% gold and 45 at.% silver does not de-alloy, but if it is re-melted with additional silver so that the atom fraction of Ag is greater than 60%, the gold can be separated almost completely by nitric acid immersion.

Type
Corrosion Science
Information
MRS Bulletin , Volume 24 , Issue 7 , July 1999 , pp. 24 - 28
Copyright
Copyright © Materials Research Society 1999

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