TY - JOUR
T1 - Effects of initial Fe2+ concentration and pulp density on the bioleaching of Cu from enargite by Acidianus brierleyi
AU - Sasaki, Keiko
AU - Takatsugi, Koichiro
AU - Hirajima, Tsuyoshi
N1 - Funding Information:
Financial support was provided to KS by the Japan Society for the Promotion of Science (JSPS Grant-in-Aid for Scientific Research No. 22246117 ), the JSPS Funding Program for Next Generation World-Leading Researchers ( GR078 ) and JSPS Invitation Fellowship Program for Research in Japan (Short Term) FY2011 (S11078) . The authors thank Dr. Yasuhiro Konishi at Osaka Prefecture University for helpful discussions regarding culture of A. brierleyi and Dr. Olli H. Tuovinen, Ohio State University, for constructive discussion regarding immobilization of arsenic in the bioleaching of arsenic-bearing sulfides. XAFS spectra were collected courtesy of Dr. Chiharu Tokoro of the Waseda University with the approval of Photon Factory of the High Energy Accelerator Research Organization (Proposal No. 2010G054). XRD and XPS measurements were performed at the Center of Advanced Instrumental Analysis, and the TEM observations were carried out at the Research Laboratory for High Voltage Electron Microscopy, Kyushu University.
PY - 2011/9
Y1 - 2011/9
N2 - To maximize Cu recovery and minimize As release during the bioleaching of enargite (Cu3AsS4) by Acidianus brierleyi at 70 °C, the initial Fe2+ ion concentration and pulp density were investigated in batch tests. A maximum Cu recovery of 91.0 ± 0.5% was obtained with an initial Fe2+ ion concentration of 1.8-2.7 g/L and a pulp density of 1.0%. As the immobilization of As depended on the formation of scorodite (FeAsO4•2H2O) and cupric arsenate, a more rapid and stable As immobilization was achieved with an initial Fe2+ ion concentration of 2.7 g/L. Thus the initial Fe2+ concentration of 2.7 g/L and 1.0% pulp density provided for a combination of As precipitation and > 90% Cu recovery. When the initial Fe2+ concentration was increased, K-jarosite (KFe3(SO4)2(OH) 6) precipitated, leading to passivation of the enargite surface. When the initial Fe2+ concentration was lowered, the Cu recovery was incomplete due to insufficient oxidation. Elevating the pulp density to 2.0% showed that the increase in Eh significantly lagged behind the exponential phase in the planktonic cell growth curve. Pulp density also clearly affected the makeup of secondary minerals in solid residues after the bioleaching of enargite. There is a tendency for dissolved Fe3+ ions to readily precipitate as potassium jarosite at relatively smaller pulp densities and as scorodite at relatively larger pulp densities.
AB - To maximize Cu recovery and minimize As release during the bioleaching of enargite (Cu3AsS4) by Acidianus brierleyi at 70 °C, the initial Fe2+ ion concentration and pulp density were investigated in batch tests. A maximum Cu recovery of 91.0 ± 0.5% was obtained with an initial Fe2+ ion concentration of 1.8-2.7 g/L and a pulp density of 1.0%. As the immobilization of As depended on the formation of scorodite (FeAsO4•2H2O) and cupric arsenate, a more rapid and stable As immobilization was achieved with an initial Fe2+ ion concentration of 2.7 g/L. Thus the initial Fe2+ concentration of 2.7 g/L and 1.0% pulp density provided for a combination of As precipitation and > 90% Cu recovery. When the initial Fe2+ concentration was increased, K-jarosite (KFe3(SO4)2(OH) 6) precipitated, leading to passivation of the enargite surface. When the initial Fe2+ concentration was lowered, the Cu recovery was incomplete due to insufficient oxidation. Elevating the pulp density to 2.0% showed that the increase in Eh significantly lagged behind the exponential phase in the planktonic cell growth curve. Pulp density also clearly affected the makeup of secondary minerals in solid residues after the bioleaching of enargite. There is a tendency for dissolved Fe3+ ions to readily precipitate as potassium jarosite at relatively smaller pulp densities and as scorodite at relatively larger pulp densities.
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U2 - 10.1016/j.hydromet.2011.06.008
DO - 10.1016/j.hydromet.2011.06.008
M3 - Article
AN - SCOPUS:84860390072
SN - 0304-386X
VL - 109
SP - 153
EP - 160
JO - Hydrometallurgy
JF - Hydrometallurgy
IS - 1-2
ER -