黄铜矿
辉铜矿
铜
斑铜矿
化学
无机化学
湿法冶金
铜提取技术
有机化学
作者
J. Avraamides,D.M. Muir,Alan Parker
出处
期刊:Hydrometallurgy
[Elsevier BV]
日期:1980-06-01
卷期号:5 (4): 325-336
被引量:17
标识
DOI:10.1016/0304-386x(80)90023-7
摘要
Chalcopyrite is reduced by solutions of copper(I) sulfate and copper(I) chloride to chalcocite (Cu2S) and bornite (Cu5FeS4) whilst the iron reports to the solution. Factors which affect the rate and efficiency of reduction are examined. The reaction is rapid on fresh surfaces of chalcopyrite but slows markedly as a film of chalcocite or bornite forms. The reduction in the presence of copper metal goes to completion and gives a material which is more readily leached by oxidising agents than is chalcopyrite. Thus 99% of the copper in the reduced chalcopyrite is leached when copper(II) sulfate in aqueous acetonitrile is the oxidising agent, whereas only 30% of the copper is leached from pure chalcopyrite under similar conditions. Concentrated solutions of copper(I) salts are less effective in reducing CuFeS2 in a heterogeneous solid-liquid reaction than is copper metal in a “galvanic” solid-solid reaction. Solutions of copper(II) sulfate plus concentrated copper(I) sulfate in dilute acetonitrile (4 M) containing copper sheets are an effective reductant for chalcopyrite.
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