J. Ndalamo, A. F. Mulaba-Bafubiandi, and B. B. Mamba, UV/visible spectroscopic analysis of CO3+ and CO2+ during the dissolution of cobalt from mixed Co-Cu oxidized ores, Int. J. Miner. Metall. Mater., 18(2011), No. 3, pp. 260-269. https://doi.org/10.1007/s12613-011-0432-y
Cite this article as:
J. Ndalamo, A. F. Mulaba-Bafubiandi, and B. B. Mamba, UV/visible spectroscopic analysis of CO3+ and CO2+ during the dissolution of cobalt from mixed Co-Cu oxidized ores, Int. J. Miner. Metall. Mater., 18(2011), No. 3, pp. 260-269. https://doi.org/10.1007/s12613-011-0432-y
J. Ndalamo, A. F. Mulaba-Bafubiandi, and B. B. Mamba, UV/visible spectroscopic analysis of CO3+ and CO2+ during the dissolution of cobalt from mixed Co-Cu oxidized ores, Int. J. Miner. Metall. Mater., 18(2011), No. 3, pp. 260-269. https://doi.org/10.1007/s12613-011-0432-y
Citation:
J. Ndalamo, A. F. Mulaba-Bafubiandi, and B. B. Mamba, UV/visible spectroscopic analysis of CO3+ and CO2+ during the dissolution of cobalt from mixed Co-Cu oxidized ores, Int. J. Miner. Metall. Mater., 18(2011), No. 3, pp. 260-269. https://doi.org/10.1007/s12613-011-0432-y
The leaching of cobalt from four-mixed Co-Cu oxidized ores containing cobalt at levels ranging from 0.5wt% to 34wt% was studied and the results has been reported. Conventional dissolution of these oxidized Co-Cu ores with diluted H2SO4 and SO2 as a reducing agent resulted in a substantial improvement in the solution based recovery of cobalt. UV/visible spectroscopic analysis of the leached solutions indicated that the increased cobalt content in the solution was a result of flushing the acidified cobalt leaching solution with SO2. Furthermore, UV/visible spectroscopy confirmed that as SO2 was flushed into the acidified leaching solution, Co3+ bearing minerals were reduced to the readily soluble Co2+ bearing minerals, and this resulted in the increase of total cobalt in the collected solution. The mechanism of the reduction of Co3+ to Co2+ bearing minerals when SO2 is flushed during the leaching of mixed Co-Cu oxidized ores, including the stability trends of Co3+, Co2+, and Cu2+ complexes, as shown by their UV/visible spectra, are also discussed.