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Matsuoka, I. (1996). Mine drainage treatment. Shigen to Sozai = Journal of the Mining and Materials Processing Institute of Japan, 112(5), 273–281.
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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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Sato, D., & Tazaki, K. (2000). Calcification treatment of mine drainage and depositional formula of heavy metals. Chikyu Kagaku = Earth Science, 54(5), 328–336.
Abstract: Depositional formula of heavy metals after disposal of the mine drainage from the Ogoya Mine in Ishikawa Prefecture, Japan, was mineralogically investigated. Strong acidic wastewater (pH 3.5) from pithead of the mine contains high concentration of heavy metals. In this mine, neutralizing coagulation treatment is going on by slaked lime (calcium hydroxides: Ca(OH) (sub 2) ). Core samples were collected at disposal pond to which the treated wastewater flows. The core samples were divided into 44 layers based on the color variation. The mineralogical and chemical compositions of each layer were analyzed by an X-ray powder diffractometer (XRD), an energy dispersive X-ray fluorescence analyzer (ED-XRF) and a NCS elemental analyzer. The upper parts are rich in brown colored layers, whereas discolored are the deeper parts. The color variation is relevant to Fe concentration. Brown colored core sections are composed of abundant hydrous ferric oxides with heavy metals, such as Cu, Zn, and Cd. On the other hand, S concentration gradually increases with depth. XRD data indicated that calcite decreases with increasing depth, and ettringite is produced at the deeper parts. Cd concentration shows similar vertical profile to those of calcite and ettringite. The results revealed that hydrous ferric oxides, calcite and ettringite are formed on deposition, whereby incorporating the heavy metals.
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