The leaching of chalcopyrite with ferric chloride |
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Authors: | Tetsuji Hirato Makoto Kinoshita Yasuhiro Awakura Hiroshi Majima |
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Affiliation: | (1) Department of Metallurgy, Kyoto University, 606 Kyoto, Japan;(2) Mitsubishi Metal Corporation, Osaka Refinery, Kita-ku, 530 Osaka, Japan |
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Abstract: | A comparative study of electrochemical leaching and chemical leaching of chalcopyrite was done to elucidate the leaching mechanism of chalcopyrite with FeCl3. The leaching rate of chalcopyrite exhibits a half order dependency on the FeCl3 concentration, whereas it is independent of the FeCl2 concentration. The mixed potential of chalcopyrite exhibits a 72 mV · decade−1 dependency upon FeCl3 concentration; no influence on the mixed potential was observed by the addition of FeCl2. In FeCl3 solutions acidified with HC1, the predominant chemical species of Fe(III) was found to be FeCl 2 u+ from equilibrium calculations. The concentration of this species is approximately proportional to the amount of FeCl3 added to the solutions. Based on these observations, an electrochemical mechanism is proposed which involves the oxidation of chalcopyrite and the reduction of FeCl 2 + , the predominant species of Fe(III). By converting the leaching rate to electric current density,i, 140 mV · decade−1 dependency of mixed potential,E, against logi is obtained. This dependency of the chemical leaching of chalcopyrite with FeCl3 as well as its activation energy agree with those for electrochemical leaching. These findings strongly support the electrochemical mechanism of FeCl3 leaching of chalcopyrite. Formerly Graduate Student, Kyoto University |
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