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Eger, P. (1995). Sulfate reduction for the treatment of acid mine drainage; Long term solution or short term fix? Sudbury '95 – Mining and the Environment, Conference Proceedings, Vols 1-3, , 515–524.
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Murayama, T. (1987). Application Of Immobilized Thiobacillus-Ferrooxidans For Large-Scale Treatment Of Acid-Mine Drainage. Methods Enzymol., 136, 530–540.
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Boonstra, J. (1999). Biological treatment of acid mine drainage. Biohydrometallurgy and the Environment toward the Mining of the 21st Century, Pt B 1999, 9, 559–567.
Abstract: In this paper experience obtained with THIOPAQ technology treating Acid Mine Drainage is described. THIOPAQ Technology involves biological sulfate reduction technology and the removal of heavy metals as metal sulfide precipitates. The technology was developed by the PAQUES company, who have realised over 350 high rate biological treatment plants world wide. 5 plants specially designed for sulfate reduction are successfully operated on a continuous base (1998 status).
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Davison, W. (1988). Neutralizing Strategies For Acid Waters – Sodium And Calcium Products Generate Different Acid Neutralizing Capacities. Water Res, 22(5), 577–583.
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Olaniran, A. O. (2006). Biostimulation and bioaugmentation enhances aerobic biodegradation of dichloroethenes. Chemosphere, 63(4), 600–608.
Abstract: The accumulation of dichloroethenes (DCEs) as dominant products of microbial reductive dechlorination activity in soil and water represent a significant obstacle to the application of bioremediation as a remedial option for chloroethenes in many contaminated systems. In this study, the effects of biostimulation and/or bioaugmentation on the biodegradation of cis- and trans-DCE in soil and water samples collected from contaminated sites in South Africa were evaluated in order to deter-mine the possible bioremediation option for these compounds in the contaminated sites. Results from this study indicate that cis- and trans-DCE were readily degraded to varying degrees by natural microbial populations in all the soil and water samples tested, with up to 44% of cis-DCE and 41% of trans-DCE degraded in the untreated soil and water samples in two weeks. The degradation rate constants ranged significantly (P < 0.05) between 0.0938 and 0.560 wk(-1) and 0.182 and 0.401 wk(-1), for cis- and trans-DCE, respectively, for the various treatments employed. A combination of biostimulation and bioaugmentation significantly increased the biodegradation of both compounds within two weeks; 14% for cis-DCE and 18% for trans-DCE degradation, above those observed in untreated soil and water samples. These findings support the use of a combination of biostimulation and bioaugmentation for the efficient biodegradation of these compounds in contaminated soil and water. In addition, the results clearly demonstrate that while naturally occurring microorganisms are capable of aerobic biodegradation of cis- and trans-DCE, biotransformation may be affected by several factors, including isomer structure, soil type, and the amount of nutrients available in the water and soil. (c) 2005 Elsevier Ltd. All rights reserved.
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