Hulshof, A. H. M., Blowes, D. W., & Douglas Gould, W. (2006). Evaluation of in situ layers for treatment of acid mine drainage: A field comparison. Water Res, 40(9), 1816–1826.
Abstract: Reactive treatment layers, containing labile organic carbon, were evaluated to determine their ability to promote sulfate reduction and metal sulfide precipitation within a tailings impoundment, thereby treating tailings effluent prior to discharge. Organic carbon materials, including woodchips and pulp waste, were mixed with the upper meter of tailings in two separate test cells, a third control cell contained only tailings. In the woodchip cell sulfate reduction rates were 500 mg L-1 a-1, (5.2 mmol L-1 a-1) this was coupled with the gradual removal of 350 mg L-1 Zn (5.4 mmol L-1). Decreased δ13CDIC values from -3‰ to as low as -12‰ indicated that sulfate reduction was coupled with organic carbon oxidation. In the pulp waste cell the most dramatic change was observed near the interface between the pulp waste amended tailings and the underlying undisturbed tailings. Sulfate reduction rates were 5000 mg L-1 a-1 (52 mmol L-1 a-1), Fe concentrations decreased by 80–99.5% (148 mmol L-1) and Zn was consistently <5 mg L-1. Rates of sulfate reduction and metal removal decreased as the pore water migrated upward into the shallower tailings. Increased rates of sulfate reduction in the pulp waste cell were consistent with decreased δ13CDIC values, to as low as -22‰, and increased populations of sulfate reducing bacteria. Lower concentrations of the nutrients, phosphorus, organic carbon and nitrogen in the woodchip material contribute to the lower sulfate reduction rates observed in the woodchip cell.
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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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Curi, A. C., Granda, W. J. V., Lima, H. M., & Sousa, W. T. (2006). Zeolites and their application in the decontamination of mine waste water. Informacion Tecnologica, 17(6), 111–118.
Abstract: This paper describes the genesis, structure and classification of natural zeolites, including their most relevant properties such as porosity, adsorption and ionic exchange. The use of natural zeolites in the treatment of effluents containing heavy metals is reviewed based on current literature. These uses are focused on mineral-metallurgical effluents and mercury pollution related to artisan mining activities. The study shows that natural zeolites are efficient in removal of heavy metals in metal mining effluents, can be produced and improved at a low cost, and can also be used to adsorb mercury vapors from ovens used to fire amalgams.
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Bamforth, S. M. (2006). Manganese removal from mine waters – investigating the occurrence and importance of manganese carbonates. Appl. Geochem., 21(8), 1274–1287.
Abstract: Manganese is a common contaminant of mine water and other waste waters. Due to its high solubility over a wide pH range, it is notoriously difficult to remove from contaminated waters. Previous systems that effectively remove Mn from mine waters have involved oxidising the soluble Mn(II) species at an elevated pH using substrates such as limestone and dolomites. However it is currently unclear what effect the substrate type has upon abiotic Mn removal compared to biotic removal by in situ micro-organisms (biofilms). In order to investigate the relationship between substrate type, Mn precipitation and the biofilm community, net-alkaline Mn-contaminated mine water was treated in reactors containing one of the pure materials: dolomite, limestone, magnesite and quartzite. Mine water chemistry and Mn removal rates were monitored over a 3-month period in continuous-flow reactors. For all substrates except quartzite, Mn was removed from the mine water during this period, and Mn minerals precipitated in all cases. In addition, the plastic from which the reactor was made played a role in Mn removal. Manganese oxyhydroxides were formed in all the reactors; however, Mn carbonates (specifically kutnahorite) were only identified in the reactors containing quartzite and on the reactor plastic. Magnesium-rich calcites were identified in the dolomite and magnesite reactors, suggesting that the Mg from the substrate minerals may have inhibited Mn carbonate formation. Biofilm community development and composition on all the substrates was also monitored over the 3-month period using denaturing gradient gel electrophoresis (DGGE). The DGGE profiles in all reactors showed no change with time and no difference between substrate types, suggesting that any microbiological effects are independent of mineral substrate. The identification of Mn carbonates in these systems has important implications for the design of Mn treatment systems in that the provision of a carbonate-rich substrate may not be necessary for successful Mn precipitation. (c) 2006 Elsevier Ltd. All rights reserved.
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Bearcock, J. M. (2006). Accelerated precipitation of ochre for mine water remediation. Geochim. Cosmochim. Acta, 70(18), A42.
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