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Matlock, M. M., Howerton, B. S., & Atwood, D. A. (2002). Chemical precipitation of heavy metals from acid mine drainage. Water Res, 36(19), 4757–4764.
Abstract: The 1,3-benzenediamidoethanethiol dianion (BDET, known commercially as MetX) has been developed to selectively and irreversibly bind soft heavy metals from aqueous solution. In the present study BDET was found to remove >90% of several toxic or problematic metals from AMD samples taken from an abandoned mine in Pikeville, Kentucky. The concentrations of metals such as iron, may be reduced at pH 4.5 from 194 ppm to below 0.009 ppm. The formation of stoichiomietric BDET-metal precipitates in this process was confirmed using X-ray powder diffraction (XRD), proton nuclear magnetic resonance (1H NMR), and infrared spectroscopy (IR).
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Catalan, L. J. J., & Yin, G. (2003). Comparison of calcite to quicklime for amending partially oxidized sulfidic mine tailings before flooding. Environ Sci Technol, 37(7), 1408–1413.
Abstract: Flooding partially oxidized mine tailings for the purpose of mitigating further oxidation of sulfide minerals and generation of acid drainage is generally preceded by treatment with alkaline amendments to prevent releasing previously accumulated acidity to the water cover. This work compares the ability of calcite (CaCO3) and quicklime (CaO), two common amendments, to establish and maintain pH conditions and dissolved metal concentrations within environmentally acceptable ranges over long time periods. Although higher initial pH values were obtained with quicklime, the pH of quicklime treated tailings decreased over time. This was attributed to the low buffering capacity of quicklime treated tailings and to the consumption of hydroxide ions by incongruent dissolution of water-insoluble iron oxyhydroxysulfate minerals. In contrast, the pH of tailings treated with calcite increased initially and then remained stable at pH approximate to 6.7. This pH behavior was due to the lower reactivity of iron oxyhydroxysulfates with calcite, the increased buffering capacity provided by bicarbonate ions, and the incomplete dissolution of calcite. Overall, calcite was found preferable to quicklime for maintaining long-term neutral pH conditions in the treated tailings. With the exception of zinc, acceptable dissolved metal concentrations were achieved with calcite treated tailings.
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Norris, R. H. (1987). Effectiveness Of Mine Rehabilitation In Relation To Water-Quality. Acta Biologica Hungarica, 38(1), 127–139.
Abstract: When mining is completed the sites may be completely restored to the originalecosystem, rehabilitated for some desirable environmental characteristics, desirable alternative ecosystemscreated or just neglected. The strategy adopted will depend on the intended uses of the parts of theenvironment (including water) affected by the mining. An example of rehabilitation of a metal mine nearthe Australian Federal Capital is used to illustrate the problems that may be encountered. These include:lack of controls while mining is underway; catastrophic events, such as the collapse of a settling dam,lack of site specific understanding of pyrite oxidation processes, particularly those that are biologicallyenhanced; the need for adequate biological information on which to base decisions to meet biologicalinformation on which to base decisions to meet biological objectives. Experience has shown that biologicalcollections such studies should be stored in museums where they will be valuable for comparisons of changesover long periods.
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Barton, C. D. (1999). Renovation of a failed constructed wetland treating acid mine drainage. Environmental Geology, 39(1), 39–50.
Abstract: Acid mine drainage (AMD) from abandoned underground mines significantly impairs water quality in the Tones Branch watershed in McCreary Co., Kentucky, USA. A 1022-m(2) surface-flow wetland was constructed in 1989 to reduce the I AMD effects, however, the system failed after six months due to insufficient utilization of the treatment area, inadequate alkalinity production and metal overloading. In an attempt to improve treatment efficiencies, a renovation project was designed incorporating two anoxic limestone drains (ALDs) and a series of anaerobic subsurface drains that promote vertical now or mine water through a successive alkalinity producing system (SAPS) of limestone beds overlain by organic compost. Analytical results from the 19-month post-renovation period are very encouraging. Mean iron concentrations have decreased from 787 to 39 mg l(-1), pH increased from 3.38 to 6.46 and acidity has been reduced from 2244 to 199 mg l(-1) (CaCO3 equivalent). Mass removal rates averaged 98% for Al, 95% for Fe, 94% for acidity, 55% for sulfate and 49% for Mn during the study period. The results indicate increased alkalinity production from limestone dissolution and longer residence time have contributed to sufficient buffering and metal retention. The combination of ALDs and SAPS technologies used in the renovation and the sequence in which they were implemented within the wetland system proved to be an adequate and very promising design for the treatment of this and other sources of high metal load AMD.
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Jong, T. (2006). Microbial sulfate reduction under sequentially acidic conditions in an upflow anaerobic packed bed bioreactor. Water Research, 40(13), 2561–2571.
Abstract: The aim of this study was to operate an upflow anaerobic packed bed reactor (UAPB) containing sulfate reducing bacteria (SRB) under acidic conditions similar to those found in acid mine drainage (AMD). The UAPB was filled with sand and operated under continuous flow at progressively lower pH and was shown to be capable of supporting sulfate reduction at pH values of 6.0, 5.0, 4.5, 4.0 and 3.5 in a synthetic medium containing 53.5 mmol l(-1) lactate. Sulfate reduction rates of 553-1052 mmol m(-3) d(-1) were obtained when the influent solution pH was progressively lowered from pH 6.0 to 4.0, under an optimal flow rate of 2.61 ml min(-1). When the influent pH was further lowered to pH 3.5, sulfate reduction was substantially reduced with only about 1% sulfate removed at a rate of 3.35 mmol m(-3) d(-1) after 20 days of operation. However, viable SRB were recovered from the column, indicating that the SRB population was capable of surviving and metabolizing at low levels even at pH 3.5 conditions for at least 20 days. The changes in conductivity in the SRB column did not always occur with changes in pH and redox potential, suggesting that conductivity measurements may be more sensitive to SRB activity and could be used as an additional tool for monitoring SRB activity. The bioreactor containing SRB was able to reduce sulfate and generate alkalinity even when challenged with influent as low as pH 3.5, indicating that such treatment systems have potential for bioremediating highly acidic, sulfate contaminated waste waters. (c) 2006 Elsevier Ltd. All rights reserved.
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