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Anonymous, Unten, L., Wildeman, T. R., & Gusek, J. J. (1998). Passive treatment for contaminants in mine waters Effluent treatment in the mining industry. In S. H. Castro, F. Vergara, & M. A. Sanchez (Eds.),. Concepcion: University of Concepcion.
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Benzaazoua, M., & Bussiere, B. (1999). Desulphurization of tailings with low neutralizing potential; kinetic study and flotation modeling. In D. Goldsack, N. Belzile, P. Yearwood, & G. Hall (Eds.), Sudbury '99; Mining and the environment II; conference proceedings.
Abstract: Environmental desulphurization is an attractive alternative for acid generating tailings management as demonstrated during the last few years. In fact, such process placed at the end of the primary treatment circuit allows to reduce greatly the amount of problematic tailings by concentrating the sulphidic fraction. Moreover, the desulphurized tailings (non-acid generating) have the geotechnical and environmental properties for being used as fine material in a cover with capillary barrier effects. To produce desulphurized tailings, non selective froth flotation is the most adapted method as shown in many previous works. Desulphurization level is fixed by tailings sulphur content (or sulphide content) and neutralization potential NP. The final residue should have enough NP to compensate for his acid generating potential AP. In this paper, the authors present the results of laboratory tests conducted in Denver cells for studying the sulphide flotation kinetics of four mine tailings which are characterized by a weak neutralization potential (under 37 kg CaCO (sub 3) /t). Tailings 1, 2, 3 and 4 contain respectively 5.27, 10, 4.25 and 16.9 sulphur Wt. %. Tailings 1 and 2 are cyanide free and are well floated at pH around 11 by using amyl xanthate as collector. Collector dosage was optimized for these tailings and the results show that Tailing 2 need more collector. However, Tailings 3 and 4, which come from a gold cyanidation process, could not provide good sulphide recovery with xanthate collector because of the pyrite depression. To overcome this problem, amine acetate was used successfully but induces important entrainment. The consumption of this collector was also optimized. The results of kinetic tests and collector dosage were combined and modeled to establish relationships which allow to estimate the desulphurization performances.
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Bliss, L. N., Sellstone, C. M., Nicholson, A. D., & Kempton, J. H. (1997). Buffering of acid rock drainage by silicate minerals.
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Blowes, D. W., Bain, J. G., Smyth, D. J., Ptacek, C. J., Jambor, J. L., Blowes, D. W., et al. (2003). Treatment of mine drainage using permeable reactive materials. Environmental Aspects of Mine Wastes, 31, 361–376.
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Blowes, D. W., Ptacek, C. J., Benner, S. G., McRae, C. W. T., Bennett, T. A., & Puls, R. W. (2000). Treatment of inorganic contaminants using permeable reactive barriers. J Contam Hydrol, 45(1-2), 123–137.
Abstract: Permeable reactive barriers are an emerging alternative to traditional pump and treat systems for groundwater remediation. This technique has progressed rapidly over the past decade from laboratory bench-scale studies to full-scale implementation. Laboratory studies indicate the potential for treatment of a large number of inorganic contaminants, including As, Cd, Cr, Cu, Hg, Fe, Mn, Mo, Ni, Pb, Se, Tc, U, V, NO3, PO4 and SO4. Small-scale field studies have demonstrated treatment of Cd, Cr, Cu, Fe, Ni, Pb, NO3, PO4 and SO4. Permeable reactive barriers composed of zero-valent iron have been used in full-scale installations for the treatment of Cr, U, and Tc. Solid-phase organic carbon in the form of municipal compost has been used to remove dissolved constituents associated with acid-mine drainage, including SO4, Fe, Ni, Co and Zn. Dissolved nutrients, including NO3 and PO4, have been removed from domestic septic-system effluent and agricultural drainage.
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