The suspension-electrolysis method was applied to driect leaching of metal sulfides. The anodic dissolution mechanism of β-ZnS in the suspension-electrolysis with a Pt anode was investigated in terms of the interfacial impedance and voltammgram on the anode. The results obtained are as follows:
(1) In a low electrode potential region in the anodic suspension-electrolysis of β-ZnS alone, the anodic reaction on the Pt anode is mainly the oxidation of H
2S due to the H
2S evolution-dissolution reaction of β-ZnS in acidic solution. The anodic reaction is controlled by charge-transfer and diffusion, simultaneously.
(2) In the anodic suspension-electrolysis, suspension-graphite particles are oxidized on the Pt anode electrochemically and have a higher potential. In the presence of β-ZnS, they restrain its dissolution with H
2S evolution, and then it is dissolved by the S
0 product-reaction by the galvanic reciprocal reactions with these oxidized graphite particles. The anodic reaction on the Pt anode in co-suspension of β-ZnS and graphite powder, is mainly the oxidation of the latter.
(3) In the presence of Fe
3+, β-ZnS is dissolved by the reaction, ZnS+2Fe
3+=Zn
2++2Fe
2++S
0. The anodic reaction on the Pt anode is mainly the oxidation of product Fe
2+ and is controlled by the charge-transfer reaction of Fe
2+/Fe
3+.
(4) Upon suspension-electrolysis of β-ZnS in co-suspending graphite powder and added Fe
3+, the oxidation current is remarkably large. The anodic reaction on the Pt anode is also mainly controlled by the charge-transfer reaction of Fe
2+/Fe
3+.
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