Dr. Dmitri Kopeliovich
Selective corrosion (dealloying, selective leaching) is a preferential attack of a particular component of an alloy in presence of electrolyte as a result of an electrochemical oxidation-reduction (redox) process.
Selective corrosion may occur in a single-phase and in multi-phase alloys.
Alloys prone to selective corrosion are composed of components with a great difference between their Electrode potentials (eg.Cu-Zn).
The component having lower value of electrode potential (higher position in the table of Electrochemical series) will oxidize (anodic reaction) and dissolve in the electrolyte when the component having higher value of electrode potential will provide cathodic reaction (reduction).
Selective corrosion may be either uniform or plug type (localized).
Selective corrosion results in formation of nano-scale porous structure on the alloy surface.
Dezincification is the loss of zinc from *Brasses (copper-zinc alloys) as a result of Selective corrosion (dealloying).
Dezincification occurs in brasses containing more than 15% of zinc.
Zinc is chemically active element. Its standard electrode potential is very low (-0.763). Standard electrode potential of copper is much higher (+0.337).
The difference between the potentials is the driving force of dezincification.
Possible mechanisms of dezincification:
Zn = Zn2+ + 2e-.
Means of preventing dezincification:
Graphitic corrosion is the selective leaching of iron from Grey cast irons.
Standard electrode potential of Graphite is higher than that of iron therfore graphite particles in grey cast irons act as cathodes in the galvanic cell graphite-iron.
Ferrite (solid solution of carbon in α-iron) dissolves in the electrolyte by anodic reaction: Fe = Fe2+ + 2e- leaving porous network of graphite flakes behind.