Abstract
A study of the rate of dissolution of chalcopyrite (CuFeS2) in acidic solutions under oxygen overpressures was carried out by measuring the rate of formation of cupric ions in solution. Effects of temperature, oxygen partial pressure, surface area, and concentration of sulfuric acid were evaluated. A sized batch of chalcopyrite was leached in the temperature range of 125 to 175° and in the pressure range of 75 to 400 psi of oxygen. In 0.5N H2SO4 all products of reaction went into solution except for trace amounts of elemental sulfur. The dissolution of chalcopyrite followed linear kinetics and was essentially independent of hydrogen ion concentration for H2SO4 concentrations between 0.2 and 0.5 JV. The oxygen dependence indicated adsorption approaching limiting values with increasing oxygen pressure. The linear mechanism was explained in terms of steady-state adsorption of oxygen at the chalcopyrite surface followed by a surface reaction. The enthalpy of activation for adsorption of oxygen was found to be approximately 33 kcal per mole. An activation enthalpy of approximately 9 kcal per mole was observed for the surface reaction. Charge transfer reaction are not rate controlling in the process.
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Yu, P.H., Hansen, C.K. & Wadsworth, M.E. A kinetic study of the leaching of chalcopyrite at elevated temperatures. Metall Trans 4, 2137–2144 (1973). https://doi.org/10.1007/BF02643279
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DOI: https://doi.org/10.1007/BF02643279