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The cathodic processes that occur on a covellite (CuS) surface in mixed sulfate–chloride solutions in the absence and presence of copper(II) ions have been studied using potentiostatic transients and cyclic voltammetry at rotating disk electrodes in the potential range 0.3–0.7 V (versus SHE). This range is relevant to the oxidative leaching of this copper mineral in sulfate and chloride lixiviants. Variations in the concentrations of sulfate and chloride ions had a small effect on the cathodic reduction of covellite in the potential range of 0.5–0.3 V, although the presence of chloride ion resulted in a significant increase in the anodic current on the reverse sweep. On the other hand, addition of copper(II) ions resulted in enhanced cathodic currents and subsequent anodic currents in both sulfate and chloride solutions due to reduction of covellite to an undefined reduced copper sulfide species. Reduction of copper(II) to copper(I) ions becomes the preferred cathodic reaction as the concentration of chloride ions increases, becoming mass transport controlled at a rotating disc electrode at potentials below about 0.4 V. Potentiostatic measurements at potentials negative to the mixed potential in acidic chloride solutions have shown that reduction of copper(II) ions is reversible and have been used to estimate the rate of oxidative dissolution of the mineral which value agrees reasonably well with previously reported leaching rates under similar conditions. Reduction of dissolved oxygen has been found to be very much slower that that of copper(II) ions under ambient conditions. [ABSTRACT FROM AUTHOR]

Thiosulfate has been considered as one of the most promising of the non-toxic alternatives to cyanide for the leaching of gold and much work has been carried out with the aim of understanding and improving the ammoniacal thiosulfate leaching process. In particular the behaviour of gold in thiosulfate solutions containing copper in the absence of ammonia has received little attention. It has been shown in this study involving electrochemical and leaching tests that copper ions catalyze not only the oxidation of thiosulfate but also the dissolution of gold in alkaline thiosulfate solutions. Electrochemical studies have shown that copper has a positive effect on the anodic dissolution of gold with increasing concentrations of copper resulting in higher dissolution rates of gold at a potential of 0.3?V. Studies on the dissolution of gold powder in alkaline oxygenated thiosulfate solutions containing low concentrations of copper have shown that the role of copper in enhancing the dissolution rate of gold is possibly associated with the formation of a copper-thiosulfate-oxygen intermediate which is more reactive in terms of cathodic reduction than dissolved oxygen. The electrochemical experiments have been complemented by a leaching study which has shown that milling of gold powder in the presence of copper (added as ions, metal, or oxide) assists with the dissolution of gold in thiosulfate solutions. [ABSTRACT FROM AUTHOR]

The anodic dissolution of gold in alkaline thiosulfate solutions has been studied by using a rotating gold disc. Experimental results have shown that the gold dissolves at measurable rates in thiosulfate solutions at potentials above 0.2 V. It has been confirmed that dissolution occurs in parallel with oxidation of thiosulfate with a dissolution current efficiency that varies with time and with the experimental conditions and which is generally in the range of 0.3 to 0.6. Although oxygen could be used as an oxidant for gold in the thiosulfate system, the rate of the cathodic reduction of oxygen in the relevant potential region is too slow for practical purposes. It was found that in the potential region investigated, thiosulfate ions undergo oxidative decomposition leaving a sulfur-like film on the surface of gold, which inhibits the rate of dissolution of gold and results in a low anodic current efficiency for the dissolution of gold. The factors (temperature, pH, thiosulfate concentration and ammonia) have been found to have positive effects on the kinetics of gold dissolution. The rates of gold dissolution in oxygenated alkaline thiosulfate solutions have been estimated to be much lower than in the copper–ammonia–thiosulfate and cyanide systems. [ABSTRACT FROM AUTHOR]