X-ray photoelectron spectroscopy (XPS), field emission scanning electron mi
croscopy (FESEM), and open circuit potentials were used to compare the size
, chemical state, and distribution of adsorbed and reduced gold from Au3+ c
hloride solution on pyrite and arsenopyrite. Many small AuO particles grow
on the arsenopyrite surface, whereas few, much larger, gold particles appea
r on pyrite. These results mimic the differences in distribution of gold in
some coexisting natural pyrites and arsenopyrites. The rate-limiting step
in deposition of gold from Au3+ chloride solutions is the reduction of Au3 to Au+, whereas the open-circuit potential for deposition is determined by
the reduction of Au+ to Au-0. The open-circuit potential of pyrite or arse
nopyrite is a corrosion potential. Presence of Au3+ shifts the corrosion po
tential to a value that depends on the relative rates of the reduction of A
u3+ and the oxidation of the mineral. Open-circuit potential measurements i
ndicate that the rate of deposition of gold on pyrite is controlled almost
entirely by the rate of reduction of Au3+. By contrast, the rate of reducti
on of gold on arsenopyrite is controlled significantly by the rate of oxida
tion of arsenopyrite.