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Author Juby, G.J.G.; Schutte, C.F. url  openurl
  Title Membrane Life in a Seeded-slurry Reverse Osmosis System Type Journal Article
  Year 2000 Publication Water Sa Abbreviated Journal  
  Volume 26 Issue 2 Pages 239-248  
  Keywords mine water treatment desalination  
  Abstract Membrane replacement can be a major operating cost of a membrane plant. During the development of a novel desalination technique (the SPARRO process) for treating calcium sulphate scaling mine waters the expected life of tubular cellulose acetate membranes operating in the seeded-slurry mode was investigated.During four operating phases of the plant over a five-year period more than 9 000 h of operating data were obtained. Performance data showed that each operating phase was dominated by either membrane fouling or membrane hydrolysis. Membrane fouling was observed to begin near the front-end of the membrane stack and proceed towards the back. Hydrolysis, on the other hand, occurred first in the tail end of the stack and moved backwards towards the Front end modules. Although two detailed membrane autopsies were carried out no definitive statement can be made in respect of the causes of either membrane hydrolysis or membrane fouling. However, suggestions are presented to explain the observed fouling phenomenon in relation to the turbidity of the pretreated feed water and the presence of chlorine. It is proposed that the presence of radioactive isotopes in the mine water which become concentrated in the process contributes to the observed membrane hydrolysis. A membrane life of up to two years is projected for an improved pretreatment arrangement.  
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  ISSN (up) 0378-4738 ISBN Medium  
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  Notes Membrane Life in a Seeded-slurry Reverse Osmosis System; Isi:000087101400013; file:///C:/Dokumente%20und%20Einstellungen/Stefan/Eigene%20Dateien/Artikel/9715.pdf; AMD ISI | Wolkersdorfer Approved no  
  Call Number CBU @ c.wolke @ 9715 Serial 8  
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Author Ueki, K.; Kotaka, K.; Itoh, K.; Ueki, A. url  openurl
  Title Potential availability of anaerobic treatment with digester slurry of animal waste for the reclamation of acid mine water containing sulfate and heavy metals Type Journal Article
  Year 1988 Publication Journal of Fermentation Technology Abbreviated Journal  
  Volume 66 Issue 1 Pages  
  Keywords mine water treatment  
  Abstract The use of an anaerobic digester slurry of cattle waste for the reclamation of acid mine water was examined. When the digester slurry was mixed with acid mine water, anaerobic digestion, including sulfate reduction and methanogenesis, was enhanced. In the mixture of acid mine water and the digester slurry, sulfate reduction proceeded without diminishing methanogenesis. The digester slurry and its supernatant (SDF-sup) showed a significant capacity to act as a strong alkaline reagent, and the pH of the acid mine water was markedly elevated by the addition of the digester slurry of SDF-sup even at the low ratio of 1% (v/v). Precipitation of heavy metals in the acid mine water occurred as the pH was elevated by the addition of SDF-sup. When the digester slurry was added at the ratio of 5% (v/v) to acid mine water which had been pretreated with SDF-sup, the rate of sulfate reduction increased with increasing the concentration of sulfate in the mixture up to about 1,400 mg·l-1. In acid mine water pretreated with SDF-sup and supplemented with the digester slurry at the ratio of 5% (v/v), the maximum amount of sulfate reduced within 20 d of incubation was about 1,000 mg·l-1, and the maximum rate of sulfate reduction was about 120 mg SO42-·l-1·d-1.  
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  ISSN (up) 0385-6380 ISBN Medium  
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  Notes Potential availability of anaerobic treatment with digester slurry of animal waste for the reclamation of acid mine water containing sulfate and heavy metals; Amsterdam [u.a.] : Elsevier; file:///C:/Dokumente%20und%20Einstellungen/Stefan/Eigene%20Dateien/Artikel/7036.pdf; Opac Approved no  
  Call Number CBU @ c.wolke @ 7036 Serial 75  
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Author Van Hille, R.P.; Boshoff, G.A.; Rose, P.D.; Duncan, J.R. url  openurl
  Title A continuous process for the biological treatment of heavy metal contaminated acid mine water Type Journal Article
  Year 1999 Publication Resour. Conserv. Recycl. Abbreviated Journal  
  Volume 27 Issue 1-2 Pages 157-167  
  Keywords mine water treatment biological treatment heavy metal acid mine water alkaline precipitation green-algae chlorella  
  Abstract Alkaline precipitation of heavy metals from acidic water streams is a popular and long standing treatment process. While this process is efficient it requires the continuous addition of an alkaline material, such as lime. In the long term or when treating large volumes of effluent this process becomes expensive, with costs in the mining sector routinely exceeding millions of rands annually. The process described below utilises alkalinity generated by the alga Spirulina sp., in a continuous system to precipitate heavy metals. The design of the system separates the algal component from the metal containing stream to overcome metal toxicity. The primary treatment process consistently removed over 99% of the iron (98.9 mg/l) and between 80 and 95% of the zinc (7.16 mg/l) and lead (2.35 mg/l) over a 14-day period (20 l effluent treated). In addition the pH of the raw effluent was increased from 1.8 to over 7 in the post-treatment stream. Secondary treatment and polishing steps depend on the nature of the effluent treated. In the case of the high sulphate effluent the treated stream was passed into an anaerobic digester at a rate of 4 l/day. The combination of the primary and secondary treatments effected a removal of over 95% of all metals tested for as well as a 90% reduction in the sulphate load. The running cost of such a process would be low as the salinity and nutrient requirements for the algal culture could be provided by using tannery effluent or a combination of saline water and sewage. This would have the additional benefit of treating either a tannery or sewage effluent as part of an integrated process.  
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  ISSN (up) 0921-3449 ISBN Medium  
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  Notes Jul; A continuous process for the biological treatment of heavy metal contaminated acid mine water; Isi:000081142100017; file:///C:/Dokumente%20und%20Einstellungen/Stefan/Eigene%20Dateien/Artikel/9937.pdf; AMD ISI | Wolkersdorfer Approved no  
  Call Number CBU @ c.wolke @ 9937 Serial 26  
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Author Tarutis Jr, W.J.; Stark, L.R.; Williams, F.M. url  openurl
  Title Sizing and performance estimation of coal mine drainage wetlands Type Journal Article
  Year 1999 Publication Ecological Engineering Abbreviated Journal  
  Volume 12 Issue 3-4 Pages 353-372  
  Keywords mine water treatment coal mine drainage constructed wetlands efficiency first-order removal loading rate removal kinetics sizing zero-order removal constructed wetlands water-quality iron kinetics removal model phosphorus retention mechanism design Wetlands and estuaries geographical abstracts: physical geography hydrology (71 6 8) acid mine drainage effluent performance assessment remediation wetland management  
  Abstract The effectiveness of wetland treatment of acid mine drainage (AMD) was assessed using three measures of performance: treatment efficiency, area-adjusted removal, and first-order removal. Mathematical relationships between these measures were derived from simple kinetic equations. Area-adjusted removal is independent of pollutant concentration (zero-order reaction kinetics), while first-order removal is dependent on concentration. Treatment efficiency is linearly related to area-adjusted removal and exponentially related to first-order removal at constant hydraulic loading rates (flow/area). Examination of previously published data from 35 natural AMD wetlands revealed that statistically significant correlations exist between several of the performance measures for both iron and manganese removal, but these correlations are potentially spurious because these measures are derived from, and are mathematical rearrangements of, the same operating data. The use of treatment efficiency as a measure of performance between wetlands is not recommended because it is a relative measure that does not account for influent concentration differences. Area-adjusted removal accounts for mass loading effects, but it fails to separate the flow and concentration components, which is necessary if removal is first-order. Available empirical evidence suggests that AMD pollutant removal is better described by first-order kinetics. If removal is first-order, the use of area-adjusted rates for determining the wetland area required for treating relatively low pollutant concentrations will result in undersized wetlands. The effects of concentration and flow rate on wetland area predictions for constant influent loading rates also depend on the kinetics of pollutant removal. If removal is zero-order, the wetland area required to treat a discharge to meet some target effluent concentration is a decreasing linear function of influent concentration (and an inverse function of flow rate). However, if removal is first-order, the required wetland area is a non-linear function of the relative influent concentration. Further research is needed for developing accurate first-order rate constants as a function of influent water chemistry and ecosystem characteristics in order to successfully apply the first-order removal model to the design of more effective AMD wetland treatment systems.  
  Address W.J. Tarutis Jr., Department of Natural Science, Lackawanna Junior College, 501 Vine Street, Scranton, PA 18509, United States  
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  ISSN (up) 0925-8574 ISBN Medium  
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  Notes Feb.; Sizing and performance estimation of coal mine drainage wetlands; 0427766; Netherlands 46; file:///C:/Dokumente%20und%20Einstellungen/Stefan/Eigene%20Dateien/Artikel/10596.pdf; Geobase Approved no  
  Call Number CBU @ c.wolke @ 10596 Serial 25  
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Author Evangelou, V.P. url  openurl
  Title Pyrite microencapsulation technologies: Principles and potential field application Type Journal Article
  Year 2001 Publication Ecological Engineering Abbreviated Journal  
  Volume 17 Issue 2-3 Pages 165-178  
  Keywords mine water treatment Acid mine drainage Acidity Alkalinity Amelioration Coating Oxidation Surface reactions  
  Abstract In nature, pyrite is initially oxidized by atmospheric O2, releasing acidity and Fe2+. At pH below 3.5, Fe2+ is rapidly oxidized by T. ferrooxidans to Fe3+, which oxidizes pyrite at a much faster rate than O2. Commonly, limestone is used to prevent pyrite oxidation. This approach, however, has a short span of effectiveness because after treatment the surfaces of pyrite particles remain exposed to atmospheric O2 and oxidation continuous abiotically. Currently, a proposed mechanism for explaining non-microbial pyrite oxidation in high pH environments is the involvement of OH- in an inner-sphere electron-OH exchange between pyrite/surface-exposed disulfide and pyrite/surface-Fe(III)(OH)n3-n complex and/or formation of a weak electrostatic pyrite/surface-CO3 complex which enhances the chemical oxidation of Fe2+. The above infer that limestone application to pyritic geologic material treats only the symptoms of pyrite oxidation through acid mine drainage neutralization but accelerates non-microbial pyrite oxidation. Therefore, only a pyrite/surface coating capable of inhibiting O2 diffusion is expected to control long-term oxidation and acid drainage production. The objective of this study was to examine the feasibility in controlling pyrite oxidation by creating, on pyrite surfaces, an impermeable phosphate or silica coating that would prevent either O2 or Fe3+ from further oxidizing pyrite. The mechanism underlying this coating approach involves leaching mine waste with a coating solution composed of H2O2 or hypochlorite, KH2PO4 or H4SiO4, and sodium acetate (NaAC) or limestone. During the leaching process, H2O2 or hypochlorite oxidizes pyrite and produces Fe3+ so that iron phosphate or iron silicate precipitates as a coating on pyrite surfaces. The purpose of NaAC or limestone is to eliminate the inhibitory effect of the protons (produced during pyrite oxidation) on the precipitation of iron phosphate or silicate and to generate iron-oxide pyrite coating, which is also expected to inhibit pyrite oxidation. The results showed that iron phosphate or silicate coating could be established on pyrite by leaching it with a solution composed of: (1) H2O2 0.018-0.16 M; (2) phosphate or silicate 10-3 to 10-2 M; (3) coating-solution pH [approximate]5-6; and (4) NaAC as low as 0.01 M. Leachates from column experiments also showed that silicate coatings produced the least amount of sulfate relative to the control, limestone and phosphate treatments. On the other hand, limestone maintained the leachate near neutral pH but produced more sulfate than the control.  
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  Notes July 01; Pyrite microencapsulation technologies: Principles and potential field application; file:///C:/Dokumente%20und%20Einstellungen/Stefan/Eigene%20Dateien/Artikel/10063.pdf; Science Direct Approved no  
  Call Number CBU @ c.wolke @ 10063 Serial 37  
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