The rate of gold dissolution was measured in clear solution using a gold ro
tating disk electrode. The data, obtained at various cyanide concentrations
, are in agreement with literature observations. The dissolution rates were
independent of electrode rotation speed for air-saturated solutions and cy
anide concentrations above 5 mol m(-3) and were well below external mass tr
ansfer-limited rates for cyanide and oxygen. An activator molecule, NMI, wa
s shown to increase the rate of dissolution and served to illustrate the im
portance of surface reactions in the dissolution mechanism. With increasing
activator concentration, the dissolution rate first increased to a maximum
value and then decreased. The optimum activator concentration at the maxim
um dissolution rate was found to be a function of the cyanide level. The re
sults suggest competitive adsorption between the activator and cyanide spec
ies.
A dissolution mechanism in which the active site contains two (or more) gol
d atoms is proposed. Dissolution kinetics are controlled by reactions on th
e crystalline gold surface in regions independent of potential and identifi
ed by measured potentials when both cyanide and oxygen are present. The dat
a are explained by crystalline surface mass transfer away from the active s
urface site followed by charge transfer and dissolution. Model predictions
are in reasonable agreement with observations. The proposed mechanism is ba
sed solely on kinetics measurements and calls attention to the need for fur
ther mechanistic research. (C) 2000 Elsevier Science B.V. All rights reserv
ed.