Gold cyanidation, using hydrogen peroxide as an oxidising agent, has been s
tudied by performing kinetic experiments, open circuit potential measuremen
ts and voltammetry. Small amounts of hydrogen peroxide make the cyanidation
rate lower than that in conventional cyanidation, but higher amounts can m
ake the cyanidation rate double. At low temperatures, the process is contro
lled by a chemical reaction, whereas at higher temperatures, it is controll
ed by diffusion with higher rates with respect to conventional gold cyanida
tion at atmospheric pressure. As the presence of hydrogen peroxide displace
s the mixed potential of cyanidation to more anodic potentials, where oxyge
n activity is nil, cyanidation can be performed under conditions of low oxy
gen pressure. In these conditions, cyanidation is established at transpassi
ve potential regions of gold anodic dissolution and the cyanidation rate is
determined by the cyanide concentration. The cyanidation rate can be tripl
ed by adding small amounts of thallium (I) ions to cyanidation with hydroge
n peroxide. (C) 1999 Elsevier Science B.V. All rights reserved.