Abstract
A mineralogical study has been carried out to identify the changes occurring in the sulphide phases during the leaching of Ni–Cu matte in CuSO4-H2SO4-O2 solutions. The unleached matte consists predominantly of Ni3S2, Cu2S and a Ni alloy. During attack by CuSO4-H2SO4-O2 media, the Ni3S2 reacts with CuSO4 and O2 to form soluble nickel, polydymite (Ni3S4) and covellite (CuS). The Cu2S present in the original matte is converted sequentially to digenite (Cu1.8S) and then to covellite; finally the covellite and Ni3S4 are oxidized to copper sulphate and nickel sulphate by O2-H2SO4. Iron present in the sulphides or in the Ni alloy also is dissolved but re-precipitates, at least in part, as ammonium jarosite. The ammonium jarosite itself seems to dissolve to a limited extent in various parts of the circuit. Oxides present in the feed pass through the processing cycle largely unaffected although extensive silicate dissolution does occur.