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Ciftci, H., & Akcil, A. (2006). Asidik maden drenajinin (AMD) giderilmesinde uygulanan biyolojik yontemler. Biological methods applied in the treatment of acid mine drainage (AMD). Madencilik = The = Journal of the Chamber of Mining Engineers of Turkey, 45(1), 35–45.
Abstract: Acidic mine drainage (AMD) is a serious environmental problem in mining areas throughout the world. AMD occurs as a result of the natural oxidation of sulfide minerals when they are exposed to oxygen and water during their disposal and storage at the mining areas. Because it includes low pH and high concentrations of dissolved metals and sulphates, AMD can potentially damage to the environment. If the formation of AMD can't be prevented and controlled, it must be collected and treated to remove acidity and reduce the concentration of heavy metals and suspended solids before its release to the environment. Different types of microorganisms in the treatment of AMD can play a very important role in the development and the application of microbiological prevention, control and treatment technologies. The purpose of this article is to give information about the passive biological methods used in the treatment and the control of AMD and the role of microorganisms in these methods.
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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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Sheoran, A. S., & Sheoran, V. (2006). Heavy metal removal mechanism of acid mine drainage in wetlands: A critical review. Minerals Engineering, 19(2), 105–116.
Abstract: Acid mine drainage (AMD) is one of the most significant environmental challenges facing the mining industry worldwide. Water infiltrating through the metal sulphide minerals, effluents of mineral processing plants and seepage from tailing dams becomes acidic and this acidic nature of the solution allows the metals to be transported in their most soluble form. The conventional treatment technologies used in the treatment of acid mine drainage are expensive both in terms of operating and capital costs. One of the methods of achieving compliance using passive treatment systems at low cost, producing treated water pollution free, and fostering a community responsibility for acid mine water treatment involves the use of wetland treatment system. These wetlands absorb and bind heavy metals and make them slowly concentrated in the sedimentary deposits to become part of the geological cycle. In this paper a critical review of the heavy metal removal mechanism involving various physical, chemical and biological processes, which govern wetland performance, have been made. This information is important for the siting and use of wetlands for remediation of heavy metals.
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Agency, U. S. E. P., & Development, O. of R. and. (2006). Active and semi-passive lime treatment of acid mine drainage at Leviathan Mine, California. Cincinnati, OH: National Risk Management Research Laboratory, Office of Research and Development, U.S. Environmental Protection Agency.
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Sasaki, K. (2006). Immobilization of Mn(II) ions by a Mn-oxidizing fungus – Paraconiothyrium sp.-like strain at neutral pHs. Mater. Trans., 47(10), 2457–2461.
Abstract: A Mn-oxidizing fungus was isolated from a constructed wetland of Hokkaido (Japan), which is receiving the Mn-impacted drainage, and genetically and morphologically identified as Paraconiothyrium sp.-like strain. The optimum pHs were 6.45-6.64, where is more acidic than those of previously reported Mn-oxidizing fungi. Too much nutrient inhibited fungal Mn-oxidation, and too little nutrient also delayed Mn oxidation even at optimum pH. In order to achieve the oxidation of high concentrations of Mn like mine drainage containing several hundreds g-m(-3) of Mn, it is important to find the best mix ratio among the initial Mn concentrations, inocolumn size and nutrient concentration. The strain has still Mn-tolerance with more than 380 g-m(-3) of Mn, but high Mn(II) oxidation was limited by pH control and supplied nutrient amounts. The biogenic Mn deposit was poorly crystallized birnessite. The strain is an unique Mn-oxidizing fungus having a high Mn tolerance and weakly acidic tolerance, since there has been no record about the property of the strain. There is a potentiality to apply the strain to the environmental bioremediation.
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