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Curi, A.C.; Granda, W.J.V.; Lima, H.M.; Sousa, W.T. |
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Title |
Zeolites and their application in the decontamination of mine waste water |
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Journal Article |
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Year |
2006 |
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Informacion Tecnologica |
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17 |
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6 |
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111-118 |
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adsorption decontamination effluents industrial waste ion exchange metallurgical industries metallurgy mining mining industry porosity wastewater treatment zeolites zeolites decontamination mine waste water genesis porosity adsorption ionic exchange mineral metallurgical effluents mercury pollution artisan mining activities heavy metals removal metal mining effluents mercury vapors ovens fire amalgams Manufacturing and Production |
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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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0716-8756 |
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Zeolites and their application in the decontamination of mine waste water; 9532002; Journal Paper; SilverPlatter; Ovid Technologies |
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Call Number |
CBU @ c.wolke @ 16784 |
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409 |
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Sheoran, A.S.; Sheoran, V. |
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Title |
Heavy metal removal mechanism of acid mine drainage in wetlands: A critical review |
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Journal Article |
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Year |
2006 |
Publication |
Minerals Engineering |
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19 |
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2 |
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105-116 |
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Acid mine drainage Metal removal mechanism Wetlands |
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Acid mine drainage (AMD) is one of the most significant environmental challenges facing the mining industry worldwide. Water infiltrating through the metal sulphide minerals, effluents of mineral processing plants and seepage from tailing dams becomes acidic and this acidic nature of the solution allows the metals to be transported in their most soluble form. The conventional treatment technologies used in the treatment of acid mine drainage are expensive both in terms of operating and capital costs. One of the methods of achieving compliance using passive treatment systems at low cost, producing treated water pollution free, and fostering a community responsibility for acid mine water treatment involves the use of wetland treatment system. These wetlands absorb and bind heavy metals and make them slowly concentrated in the sedimentary deposits to become part of the geological cycle. In this paper a critical review of the heavy metal removal mechanism involving various physical, chemical and biological processes, which govern wetland performance, have been made. This information is important for the siting and use of wetlands for remediation of heavy metals. |
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Heavy metal removal mechanism of acid mine drainage in wetlands: A critical review; Science Direct |
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CBU @ c.wolke @ 17252 |
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41 |
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Potgieter-Vermaak, S.S.; Potgieter, J.H.; Monama, P.; Van Grieken, R. |
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Comparison of limestone, dolomite and fly ash as pre-treatment agents for acid mine drainage |
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Journal Article |
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2006 |
Publication |
Minerals Engineering |
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19 |
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5 |
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454-462 |
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Acid rock drainage Mining Tailings Environmental |
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The physical, chemical and biological nature of Vaal Dam water, the main source of water in Gauteng, South Africa, is often affected by underground water pollution (acid mine water) and industrial effluents. The ecological significance and detrimental effects necessitate investigations into treating the water prior to discharge into public streams. Although several acid mine water treatment techniques and methods exist, they all have certain disadvantages. Lime treatment is the most common approach. In this investigation, limestone, dolomite and fly ash were selected as pre-treatment agents based on their low cost. Simulated acid mine water containing these agents was tested using a Jar Test apparatus. Samples were analyzed before and after treatment for pH, ferrous, ferric, calcium, magnesium and sulphate ions. The study demonstrated that the quality of the water improved with an increase in the amount and surface area of the raw material dosed and an increase in contact time. It was also influenced by the chemical composition of the acid mine water and aeration. Chemical cost savings of 38% are achieved when lime is replaced with limestone, and cost savings of 23% and 48% can be accomplished when limestone is substituted with dolomite and fly ash respectively. This could result in significant savings to the gold and coal mining industries, and could lead to a mutual benefit/gain between industrialists/polluters and the public. |
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0892-6875 |
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Apr.; Comparison of limestone, dolomite and fly ash as pre-treatment agents for acid mine drainage; Science Direct |
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CBU @ c.wolke @ 17461 |
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42 |
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Conca, J.L.; Wright, J. |
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An Apatite II permeable reactive barrier to remediate groundwater containing Zn, Pb and Cd |
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Journal Article |
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2006 |
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Appl. Geochem. |
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21 |
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12 |
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2188-2200 |
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Pollution and waste management non radioactive Groundwater quality apatite groundwater remediation zinc lead cadmium acid mine drainage copper sulfate nitrate permeability water treatment precipitation chemistry |
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Phosphate-induced metal stabilization involving the reactive medium Apatite II(TM) [Ca10-xNax(PO4)6-x(CO3)x(OH)2], where x < 1, was used in a subsurface permeable reactive barrier (PRB) to treat acid mine drainage in a shallow alluvial groundwater containing elevated concentrations of Zn, Pb, Cd, Cu, SO4 and NO3. The groundwater is treated in situ before it enters the East Fork of Ninemile Creek, a tributary to the Coeur d'Alene River, Idaho. Microbially mediated SO4 reduction and the subsequent precipitation of sphalerite [ZnS] is the primary mechanism occurring for immobilization of Zn and Cd. Precipitation of pyromorphite [Pb10(PO4)6(OH,Cl)2] is the most likely mechanism for immobilization of Pb. Precipitation is occurring directly on the original Apatite II. The emplaced PRB has been operating successfully since January of 2001, and has reduced the concentrations of Cd and Pb to below detection (2 μg L-1), has reduced Zn to near background in this region (about 100 μg L-1), and has reduced SO4 by between 100 and 200 mg L-1 and NO3 to below detection (50 μg L-1). The PRB, filled with 90 tonnes of Apatite II, has removed about 4550 kg of Zn, 91 kg of Pb and 45 kg of Cd, but 90% of the immobilization is occurring in the first 20% of the barrier, wherein the reactive media now contain up to 25 wt% Zn. Field observations indicate that about 30% of the Apatite II material is spent (consumed). |
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0883-2927 |
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Dec.; An Apatite II permeable reactive barrier to remediate groundwater containing Zn, Pb and Cd; Science Direct |
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CBU @ c.wolke @ 17248 |
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44 |
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Bamforth, S.M. |
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Title |
Manganese removal from mine waters – investigating the occurrence and importance of manganese carbonates |
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Journal Article |
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2006 |
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Appl. Geochem. |
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21 |
Issue |
8 |
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1274-1287 |
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mine water treatment |
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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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Manganese removal from mine waters – investigating the occurrence and importance of manganese carbonates; Wos:000240297600004; Times Cited: 0; ISI Web of Science |
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CBU @ c.wolke @ 16916 |
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107 |
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