Removal of copper from aqueous solution by electrodeposition in cathode chamber of microbial fuel cell

Based on energetic analysis, a novel approach for copper electrodeposition via cathodic reduction in microbial fuel cells (MFCs) was proposed for the removal of copper and recovery of copper solids as metal copper and/or Cu 2O in a cathode with simultaneous electricity generation with organic matter...

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Veröffentlicht in:Journal of hazardous materials 2011-05, Vol.189 (1), p.186-192
Hauptverfasser: Tao, Hu-Chun, Liang, Min, Li, Wei, Zhang, Li-Juan, Ni, Jin-Ren, Wu, Wei-Min
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Sprache:eng
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Zusammenfassung:Based on energetic analysis, a novel approach for copper electrodeposition via cathodic reduction in microbial fuel cells (MFCs) was proposed for the removal of copper and recovery of copper solids as metal copper and/or Cu 2O in a cathode with simultaneous electricity generation with organic matter. This was examined by using dual-chamber MFCs (chamber volume, 1 L) with different concentrations of CuSO 4 solution (50.3 ± 5.8, 183.3 ± 0.4, 482.4 ± 9.6, 1007.9 ± 52.0 and 6412.5 ± 26.7 mg Cu 2+/L) as catholyte at pH 4.7, and different resistors (0, 15, 390 and 1000 Ω) as external load. With glucose as a substrate and anaerobic sludge as an inoculum, the maximum power density generated was 339 mW/m 3 at an initial 6412.5 ± 26.7 mg Cu 2+/L concentration. High Cu 2+ removal efficiency (>99%) and final Cu 2+ concentration below the USA EPA maximum contaminant level (MCL) for drinking water (1.3 mg/L) was observed at an initial 196.2 ± 0.4 mg Cu 2+/L concentration with an external resistor of 15 Ω, or without an external resistor. X-ray diffraction analysis confirmed that Cu 2+ was reduced to cuprous oxide (Cu 2O) and metal copper (Cu) on the cathodes. Non-reduced brochantite precipitates were observed as major copper precipitates in the MFC with a high initial Cu 2+ concentration (0.1 M) but not in the others. The sustainability of high Cu 2+ removal (>96%) by MFC was further examined by fed-batch mode for eight cycles.
ISSN:0304-3894
1873-3336
DOI:10.1016/j.jhazmat.2011.02.018