St-Arnaud, L. C. (1994). Water covers for the decommissioning of sulfidic mine tailings impoundments. In Special Publication – United States. Bureau of Mines, Report: BUMINES-SP-06A-94 (pp. 279–287). 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.
|
Sottnik, P., & Sucha, V. (2001). Moznosti upravy kysleho banskeho vytoku loziska Banska Stiavnica-Sobov. Remediation of acid mine drainage from Sobov Mine, Banska Stiavnica. Mineralia Slovaca, 33(1), 53–60.
Abstract: A waste dump formed during the exploitation of quartzite deposit in Sobov mine (Slovakia) produces large quantity of acid mine drainage (AMD) which is mainly a product of pyrite oxidation. Sulphuric acid--the most aggressive oxidation product--attacks gangue minerals, mainly clays, as well. This process lead to a sharp decrease of the pH values (2-2.5) and increase of Fe, Al and SO (super 2-) (sub 4) contents (TDS = 20-30 mg/1). Passive treatment system was designed to remediate AMD. Chemical redox reactions along with microbial activity cause a precipitation of mobile contamination into a more stable forms. The sulphides are formed in the anaerobic cell, under reducing conditions. Fe-, Al- oxyhydroxides are precipitated in the aerobic part of the system. Precipitation decreases the Fe and Al contents along with immobilization of some heavy metal closely related to oxyhydroxides. Besides oxidation, the wetland vegetation is an active part of on aerobic cell. The system has been working effectively since September 1999. The pH values of outflowing water are apparently higher (6.2-6.8) and contents of dissolved elements (Fe from 2.260 to 4.1; Al from 900 to 0.18; Mn from 51 to 23; Cu from 4.95 to 0.03 mg/l) is significantly lowers.
|
Schwartz, M. O., & Ploethner, D. (1999). From mine water to drinking water; heavy-metal removal by carbonate precipitation in the Grootfontein-Omatako Canal, Namibia.. Hanover: Bundesanst. fuer Geowiss. und Rohstoffe.
|
Scharp, R. A., Kawahara, F., Burckle, J., Allan, J., & Govind, R. (2002). Recovery of metals from acid mine drainage Hardrock mining 2002; issues shaping the industry..
|
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.
|