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Diz, H. R. (1997). Chemical and biological treatment of acid mine drainage for the removal of heavy metals and acidity. Ph.D. thesis, Virginia Polytechnic Institute and State University,, Blacksburg.
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Banks, D., Younger, P. L., Arnesen, R. - T., Iversen, E. R., & Banks, S. B. (1997). Mine-water chemistry: The good, the bad and the ugly. Environ. Geol., 32(3), 157–174.
Abstract: Contaminative mine drainage waters have become one of the major hydrogeological and geochemical problems arising from mankind's intrusion into the geosphere. Mine drainage waters in Scandinavia and the United Kingdom are of three main types: (1) saline formation waters; (2) acidic, heavy-metal-containing, sulphate waters derived from pyrite oxidation, and (3) alkaline, hydrogen-sulphide-containing, heavy-metal-poor waters resulting from buffering reactions and/or sulphate reduction. Mine waters are not merely to be perceived as problems, they can be regarded as industrial or drinking water sources and have been used for sewage treatment, tanning and industrial metals extraction. Mine-water problems may be addressed by isolating the contaminant source, by suppressing the reactions releasing contaminants, or by active or passive water treatment. Innovative treatment techniques such as galvanic suppression, application of bactericides, neutralising or reducing agents (pulverised fly ash-based grouts, cattle manure, whey, brewers' yeast) require further research.
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Turek, M., & Gonet, M. (1997). Nanofiltration in the utilization of coal-mine brines. Desalination, 108(1-3), 171–177.
Abstract: The utilization of saline coal mine waters is considered to be the most adequate method of solving ecological problems caused by this kind of water in Poland. In the case of most concentrated waters, the so-called coalmine brines, the method of concentrating by evaporation in a twelve-stage expansion installation or vapour compression is applied, after which sodium chloride is manufactured. A considerable restriction in the utilization of coal mine brines is the high energy consumption in these methods of evaporation. An obstacle in the application of low energy evaporation processes, e.g. multi-stage flash, is the high concentration of calcium and sulfate ions in the coal mine brines. The present paper deals with the application of nanofiltration in the pretreatment of the brine. The application of nanofiltration membranes with an adequate pore size, including charged membranes, makes it possible to decrease the concentration of divalent ions in the permeate practically without any changes in the concentration of sodium chloride. Then the permeate may be concentrated in a multi-stage evaporation process, e.g. MSF, without any risk of the crystallization of gypsum. A combination of NF and MSF ought to set down the unit costs of the concentration of coal mine brines below those of mere evaporation.
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Benner, S. G., Blowes, D. W., & Ptacek, C. J. (1997). A full-scale porous reactive wall for prevention of acid mine drainage. Ground Water Monitoring and Remediation, 17(4), 99–107.
Abstract: The generation and release of acidic drainage containing high concentrations of dissolved metals from decommissioned mine wastes is an environmental problem of international scale. A potential solution to many acid drainage problem is the installation of permeable reactive walls into aquifers affected by drainage water derived from mine waste materials. A permeable reactive wall installed into an aquifer impacted by low-quality mine drainage waters was installed in August 1995 at the Nickel Rim mine site near Sudbury, Ontario. The reactive mixture, containing organic matter, was designed to promote bacterially mediated sulfate reduction and subsequent metal sulfide precipitation. The reactive wall is installed to an average depth of 12 feet (3.6 m) and is 49 feet (15 m) long perpendicular to ground water flow. The wall thickness (flow path length) is 13 feet (4 m). Initial results, collected nine months after installation, indicate that sulfate reduction and metal sulfide precipitation is occurring. Comparing water entering the wall to treated water existing the wall, sulfate concentrations decrease from 2400 to 4600 mg/L to 200 to 3600 mg/L; Fe concentration decrease from 250 to 1300 mg/L to 1.0 to 40 mg/L, pH increases from 5.8 to 7.0; and alkalinity (as CaCO<inf>3</inf>) increases from 0 to 50 mg/L to 600 to 2000 mg/L. The reactive wall has effectively removed the capacity of the ground water to generate acidity on discharge to the surface. Calculations based on comparison to previously run laboratory column experiments indicate that the reactive wall has potential to remain effective for at least 15 years.
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Barton, C. D., & Karathanasis, A. D. (1997). Aerobic and anaerobic metal attenuation processes in a constructed wetland treating acid mine drainage. In AAPG Eastern Section and the Society for Organic Petrology joint meeting; abstracts (1545). 81: AAPG Bulletin.
Abstract: The use of constructed wetlands for acid mine drainage amelioration has become a popular alternative to conventional treatment methods, however, the metal attenuation processes of these systems are poorly understood. Precipitates from biotic and abiotic zones of a staged constructed wetland treating high metal load (approx. equal to 1000 mg L (super -1) ) and low pH (approx. 3.0) acid mine drainage were characterized by chemical dissolution, x-ray diffraction, thermal analysis and scanning electron microscopy. Characterization of abiotic/aerobic zones within the treatment system suggest the presence of crystalline iron oxides and hydroxides such as hematite, lepidocrocite, goethite, and jarosite. At the air/water interface of initial abiotic treatment zones, SO (sub 4) /Fe ratios were low enough (<2.0) for the formation of jarosite and goethite, but as the ratio increased due to treatment and subsequent reductions in iron concentration, jarosite was transformed to other Fe-oxyhydroxysulfates and goethite formation was inhibited. In addition, elevated pH conditions occurring in the later stages of treatment promoted the formation of amorphous iron oxyhydroxides. Biotic wetland cell substrate characterizations suggest the presence of amorphous iron minerals such as ferrihydrite and Fe(OH) (sub 3) . Apparently, high Fe (super 3+) activity, low Eh and low oxygen diffusion rates in the anaerobic subsurface environment inhibit the kinetics of crystalline iron precipitation. Some goethite, lepidocrocite and hematite, however, were observed near the surface in biotic areas and are most likely attributable to increased oxygen levels from surface aeration and/or oxygen transport by plant roots. Alkalinity generation from limestone dissolution within the substrate and bacterially mediated sulfate reduction also has a significant role on the mineral retention process. The formation of gypsum, rhodochrocite and siderite are by-products of alkalinity generating reactions in this system and may have an impact on S, Mn, and Fe solubility controls. Moreover, the buffering of acidity through excess alkalinity appears to facilitate the precipitation and retention of metals within the system.
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