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Bloom, N. S., Preus, E., Kilner, P. I., von der Geest, E., & Hensman, C. E. (2002). Very efficient removal of toxic metals from acid mine drainage water (Berkeley Pit, Montana) with a recycled alkaline industrial waste product Hardrock mining 2002; issues shaping the industry..
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Adam, K. (2003). Solid wastes management in sulphide mines: From waste characterisation to safe closure of disposal sites. Minerals and Energy Raw Materials Report, 18(4), 25–35.
Abstract: Environmentally compatible Waste Management schemes employed by the European extractive industry for the development of new projects, and applied in operating sulphide mines, are presented in this study. Standard methodologies used to assess the geotechnical and geochemical properties of the solid wastes stemming from mining and processing of sulphidic metal ores are firstly given. Based on waste properties, the measures applied to ensure the environmentally safe recycling and disposal of sulphidic wastes are summarised. Emphasis is given on the novel techniques developed to effectively prevent and mitigate the acid drainage phenomenon from sulphidic mine wastes and tailings. Remediation measures taken to minimise the impact from waste disposal sites in the post-closure period are described.
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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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Akcil, A., & Koldas, S. (2006). Acid Mine Drainage (AMD): causes, treatment and case studies. J. Cleaner Prod., 14(12-13), 1139–1145.
Abstract: This paper describes Acid Mine Drainage (AMD) generation and its associated technical issues. As AMD is recognized as one of the more serious environmental problems in the mining industry, its causes, prediction and treatment have become the focus of a number of research initiatives commissioned by governments, the mining industry, universities and research establishments, with additional inputs from the general public and environmental groups. In industry, contamination from AMD is associated with construction, civil engineering mining and quarrying activities. Its environmental impact, however, can be minimized at three basic levels: through primary prevention of the acid-generating process; secondary control, which involves deployment of acid drainage migration prevention measures; and tertiary control, or the collection and treatment of effluent.
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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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