
TY  - JOUR
A1  - Beattie, JK 
A1  - Polyblank, GA 
T1  - Copper-Catalyzed Oxidation of Cyanide by Peroxide in Alkaline Aqueous Solution
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1995
VL  - 48
IS  - 4
SP  - 861
EP  - 868
KW  - 
UR  - https://doi.org/10.1071/CH9950861 
N2  - The oxidation of cyanide by peroxide in alkaline aqueous solution is catalysed by copper complexes. In the presence of excess cyanide, copper(II) is reduced to form the tricyanocuprate (I) complex. The cyanogen oxidation product is hydrolysed with disproportionation to cyanate and cyanide:2CuII+2CN-&#8594; 2CuI+(CN)2(CN)2+2OH- &#8594; OCN-+CN-+H2OCuI+3CN- &#8596; Cu(CN)32-The stoichiometry and kinetics of the catalysed oxidation have been investigated. Hydrogen peroxide oxidizes coordinated cyanide with a rate that is first order in peroxide and first order in copper but independent of cyanide concentration in the presence of excess cyanide. Cu(CN)32-+H2O2&#8594; Cu(CN)2-+OCN-+H2O Cu(CN)2-+CN-&#8596; Cu(CN)32- When the excess cyanide is consumed and Cu(CN)2- becomes the dominant species, the reaction becomes more complex and less efficient. Under certain conditions the stoichiometry revealed a peroxide-to-Cu(CN)2- ratio of about 6 : 1, instead of the minimum of 2.5:1 required for the oxidation of the coordinated cyanide to cyanate and the CuI to Cu(OH)2. This suggests that peroxide is consumed by a copper- catalysed  disproportionation, in competition with oxidation of the coordinated cyanide. An intermediate yellow complex forms while peroxide is present, before Cu(OH)2 finally precipitates. The consequence of this mechanism is that the most efficient process for the destructive oxidation of cyanide has a high cyanide-to-copper ratio, to minimize the final concentration of Cu(CN)2- which consumes peroxide inefficiently. The rate of the reaction depends on the concentration of copper, however, which must be large enough for a satisfactory turnover. 
ER  -

