The electrochemical oxidation of alkaline copper cyanide solutions

被引:53
作者
Cheng, SC [1 ]
Gattrell, M [1 ]
Guena, T [1 ]
MacDougall, B [1 ]
机构
[1] Natl Res Council Canada, Inst Chem Proc & Environm Technol, Ottawa, ON K1A 0R6, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
cyanide oxidation; copper complexes; hydroxide ions; copper oxide and nitrate;
D O I
10.1016/S0013-4686(02)00200-1
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
A systematic investigation of the electrochemical oxidation of copper cyanide was carried out. At low pH cyanide destruction is believed to be catalyzed by the heterogeneous reaction involving adsorbed [Cu(CN)(3)](2-) and possibly [Cu(CN)(4)](3-). At high pH, rapid oxidation of cyanide was observed hound 0.75 V versus Hg/HgO with the formation of a black copper oxide film. This enhanced electrocatalytic activity is believed to be related to the formation of an active copper(III) species. The transition point between low and high pH as a function of cyanide and copper concentrations is discussed. Bulk electrolysis of a copper cyanide solution at 0.90 V oxidized most of the cyanide to cyanate. Prolonged electrolysis further oxidized the cyanate to nitrate. The copper oxide film is found to be catalytic, capable of electro-oxidizing hydroxide to oxygen and cyanate to nitrate. (C) 2002 Published by Elsevier Science Ltd.
引用
收藏
页码:3245 / 3256
页数:12
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