中國(guó)有色金屬學(xué)報(bào)(英文版)
Transactions of Nonferrous Metals Society of China
| Vol. 26 No. 9 September 2016 |
（1. School of Minerals Processing and Bioengineering, Central South University, Changsha 410083, China;
2. Key Lab of Biometallurgy Ministry of Education, Central South University, Changsha 410083, China;
3. Shanghai Synchrotron Radiation Facility, Shanghai Institute of Applied Physics,
Chinese Academy of Sciences, Shanghai 201204, China;
4. Beijing Synchrotron Radiation Facility, Institute of High Energy Physics,
Chinese Academy of Sciences, Beijing 100049, China）
Abstract:The formation and evolution of secondary minerals during bioleaching of chalcopyrite by thermoacidophilic Archaea Acidianus manzaensis were analyzed by combining synchrotron radiation X-ray diffraction (SR-XRD) and S, Fe and Cu Kα X-ray absorption near edge structure (XANES) spectroscopy. Leaching experiment showed that 82.4% of Cu2+ was dissolved by A. manzaensis after 10 d. The surface of chalcopyrite was corroded apparently and covered with leaching products. During bioleaching, the formation and evolution of secondary minerals were as follows: 1) little elemental sulfur, jarosite, bornite and chalcocite were found at days 2 and 4; and 2) bornite and chalcocite disappeared, covellite formed, and jarosite gradually became the main component at days 6 and 10. These results indicated that metal-deficiency sulfides chalcocite and bornite were first formed with a low redox potential value (360-461 mV), and then gradually transformed to covellite with a high redox potential value (461-531 mV).
Key words: bioleaching; chalcopyrite; Acidianus manzaensis; secondary minerals; formation; evolution
