Electrochemistry of copper in aqueous acetonitrile

Abstract

The electrochemical characteristics of the Cu (II)/Cu (I) and the Cu (I)/Cu (0) couples at platinum, carbon, mercury and copper have been studied in acetonitrile-water (AN-H₂O) mixtures. All the electrode processes are moderately fast with mercury the fastest but slower on platinum and carbon paste in that order. A slow chemical step precedes oxidation of Cu (I) to Cu (II) on allectrodes in solutions of high AN content. The slow step may be partial removal of AN from the solvated Cu (I) ion prior to electron transfer. Electrode processes are faster in chloride ions than in sulfate ion solutions. Reduction of Cu (I) in AN−H₂O is quite slow on glassy carbon. Adsorption of AN on platinum and carbon influences the processes. Diffusion coefficients in sulfate solutions are in the order, Cu (I) (AN−H₂O)>Cu (II)(AN−H₂O)>Fe (III)(H₂O) and 2-hydroxy-cyanoethane (2-HCE) strongly decreases the mobility of Cu (I) when added to H₂O. The relevance of the measurements to hydrometallurgical processes is considered. CuSO₄ in 30% v/v AN−H₂O is a ‘faster’ oxidant than the common oxidant Fe₂(SO₄)₃ in H₂O because of the greater mobility and faster electron acceptance from a corroding surface of Cu (II). Only in solutions of very high nitrile content is the reduction potential of CuSO₄ as high as that of Fe₂(SO₄)₃ in H₂O.