Reaction mechanism for the acid ferric sulfate leaching of chalcopyrite |
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Authors: | P B Munoz J D Miller M E Wadsworth |
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Affiliation: | (1) Organization of American States,Universidad Central de Venezuela, Venezuela, Caracas;(2) University of Utah, 84112 Salt Lake City, UT |
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Abstract: | The acid ferric sulfate leaching of chalcopyrite, CuFeS2 + 4Fe+3 = Cu+2 + 5Fe+2 + 2S0 was studied using monosize particles in a well stirred reactor at ambient pressure and dilute solid phase concentration in
order to obtain fundamental details of the reaction kinetics. The principal rate limiting step for this electrochemical reaction
appears to be a transport process through the elemental sulfur reaction product. This conclusion has been reached in other
investigations and is supported by data from this investigation in which the reaction rate was found to have an inverse second
order dependence on the initial particle diameter. Furthermore, the reaction kinetics were found to be independent of Fe+3, Fe+2, Cu+2 and H2SO4 in the range of additions studied. The unique aspect of this particular research effort is that data analysis, using the
Wagner theory of oxidation, suggests that the rate limiting process may be the transport of electrons through the elemental
sulfur layer. Predicted reaction rates calculated from first principles using the physicochemical properties of the system
(conductivity of elemental sulfur and the free energy change for the reaction) agree satisfactorily with experimentally determined
rates. Further evidence which supports this analysis includes an experimental activation energy of 20 kcal/mol (83.7 kJ/mol)
which is approximately the same as the apparent activation energy for the transfer of electrons through elemental sulfur,
23 kcal/ mol (96.3 kJ/mol) calculated from both conductivity and electron mobility measurements reported in the literature.
formerly Metallurgy Graduate Student, University of Utah. |
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