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Kuyucak, N. (2001). Acid mining drainage prevention and control. Mining Environmental Management, 9(1), 12–15.
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LaPointe, F., Fytas, K., & McConchie, D. (2005). Using permeable reactive barriers for the treatment of acid rock drainage. International journal of surface mining, reclamation and environment, 19(1), 57–65.
Abstract: Acid mine drainage (AMD) is the most serious environmental problem facing the Canadian mineral industry today. It results from oxidation of sulphide minerals (e.g. pyrite or pyrrhotite) contained in mine waste or mine tailings and is characterized by acid effluents rich in heavy metals that are released into the environment. A new acid remediation technology is presented, by which metallurgical residues from the aluminium extraction industry are used to construct permeable reactive barriers (PRBs) to treat acid mine effluents. This technology is very promising for treating acid mine effluents in order to decrease their harmful environmental effects
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Miller, S. D. (1999). Overview of acid mine drainage issues and control strategies Remediation and management of degraded lands. In M. H. Wong, J. W. C. Wong, & A. J. M. Baker (Eds.),. Boca Raton: Lewis Publishers.
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Murdock, D. J., Fox, J. R. W., & Bensley, J. G. (1994). Treatment of acid mine drainage by the high density sludge process. In Special Publication – United States. Bureau of Mines, Report: BUMINES-SP-06A-94 (pp. 241–249). Proceedings of the International land reclamation and mine drainage conference and Third international conference on The abatement of acidic drainage; Volume 1 of 4; Mine drainage.
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Nakazawa, H. (2006). Treatment of acid mine drainage containing iron ions and arsenic for utilization of the sludge. Sohn International Symposium Advanced Processing of Metals and Materials, Vol 9, , 373–381.
Abstract: An acid mine drainage in abandoned Horobetsu mine in Hokkaido, Japan, contains arsenic and iron ions; total arsenic ca.10ppm, As(III) ca. 8.5ppm, total iron 379ppm, ferrous iron 266ppm, pH1.8. Arsenic occurs mostly as arsenite (As (III)) or arsenate (As (V)) in natural water. As(III) is more difficult to be remove than As(V), and it is necessary to oxidize As(III) to As(V) for effective removal. 5mL of the mine drainage or its filtrate through the membrane filter (pore size 0.45 mu m) were added to arsenite solutions (pH1.8) with the concentration of 5ppm. After the incubation of 30 days, As(III) was oxidized completely with the addition of the mine drainage while the oxidation did not occur with the addition of filtrate, indicating the microbial oxidation of As(III). In this paper, we have investigated the microbial oxidation of As(III) in acid water below pH2.0.
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