Abstract

The reaction for the ammonia, oxidation leaching of chalcopyrite, CuFeS2 + 4NH3 + 17/4 O2 + 2 OH- ⇌ Cu(NH3)+242 + l/2Fe2O3 + 2 SO4 + H2O was studied using monosize particles in an intensely stirred reactor under moderate pressures to determine the important chemical factors which govern the kinetic response of the system. The reaction kinetics were studied at dilute solid phase concentration so that oxygen transport at the gas/liquid interface would not limit the rate. A catalytic electrochemical surface reaction was shown to control the reaction kinetics with the reaction rate determined by the following equation derived from electrochemical considerations: dα/dl=127 f/do (OH-1/2 (k1PO1/1+k2PO1 (k1+k2(Cu+2)o+k’2α)(1-α)2/3 (K P 1/2 Excellent agreement between theory and experiment was obtained both with regard to apparent reaction orders for oxygen, cupric, and hydroxyl, and with regard to geometric factors that influence the reaction rate. Further support for the reaction mechanism included an activation energy of approximately 10 kcal/mole obtained under a variety of experimental conditions and the fact that the initial reaction rate constant was several orders of magnitude less than predicted mass transfer coefficients.

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