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Author Zhuang, J.M. url  openurl
  Title Lignor(TM) process for acidic rock drainage treatment Type Journal Article
  Year 2004 Publication Environ. Technol. Abbreviated Journal  
  Volume 25 Issue 9 Pages 1031-1040  
  Keywords mine water treatment  
  Abstract The process using lignosulfonates for acidic rock drainage (ARD) treatment is referred to as the Lignor(TM) process. Lignosulfonates are waste by-products produced in the sulfite pulping process. The present study has shown lignosulfonates are able to protect lime from developing an external surface coating, and hence to favor its dissociation. Further, the addition of lignosulfonates to ARD solutions increased the clotting and settling rate of the formed sludge. The capability of lignosulfonates to form stable metal-lignin complexes makes them very useful in retaining metal ions and thus improving the long-term stability of the sludge against leaching. The Lignor(TM) process involves metal sorption with lignosulfonates, ARD neutralization by lime to about pH 7, pH adjustment with caustic soda to 9.4 – 9.6, air oxidation to lower the pH to a desired level, and addition of a minimum amount of FeCl3 for further removal of dissolved metals. The Lignor(TM) process removes all concerned metals (especially Al and Mn) from the ARD of the Britannia Mine (located at Britannia Beach, British Columbia, Canada) to a level lower than the limits of the B.C. Regulations. Compared with the high-density sludge (HDS) process, the Lignor(TM) process has many advantages, such as considerable savings in lime consumption, greatly reduced sludge volume, and improved sludge stability.  
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  Notes (up) Lignor(TM) process for acidic rock drainage treatment; Wos:000224971800006; Times Cited: 0; ISI Web of Science Approved no  
  Call Number CBU @ c.wolke @ 16998 Serial 117  
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Author Bosman, D.J. url  openurl
  Title Lime Treatment Of Acid-Mine Water And Associated Solids Liquid Separation Type Journal Article
  Year 1983 Publication Water Sci. Technol. Abbreviated Journal  
  Volume 15 Issue 2 Pages 71-84  
  Keywords mine water treatment  
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  Notes (up) Lime Treatment Of Acid-Mine Water And Associated Solids Liquid Separation; Wos:A1983qg97300005; Times Cited: 7; ISI Web of Science Approved no  
  Call Number CBU @ c.wolke @ 14794 Serial 95  
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Author Sibrell, P.L. url  openurl
  Title Limestone fluidized bed treatment of acid-impacted water at the Craig Brook National Fish Hatchery, Maine, USA Type Journal Article
  Year 2006 Publication Aquacultural Engineering Abbreviated Journal  
  Volume 34 Issue 2 Pages 61-71  
  Keywords mine water treatment  
  Abstract Decades of atmospheric acid deposition have resulted in widespread lake and river acidification in the northeastern U.S. Biological effects of acidification include increased mortality of sensitive aquatic species Such as the endangered Atlantic salmon (Salmo salar). The purpose of this paper is to describe the development of a limestone-based fluidized bed system for the treatment of acid-impacted waters. The treatment system was tested at the Craig Brook National Fish Hatchery in East Orland, Maine over a period of 3 years. The product water from the treatment system was diluted with hatchery water to prepare water supplies with three different levels of alkalinity for testing of fish health and Survival. Based on positive results from a prototype system used in the first year of the study, a larger demonstration system was used in the second and third years with the objective of decreasing operating costs. Carbon dioxide was used to accelerate limestone dissolution, and was the major factor in system performance, as evidenced by the model result: Alk = 72.84 X P(CO2)(1/2); R-2 = 0.975. No significant acidic incursions were noted for the control water over the course of the Study. Had these incursions occurred, survivability in the untreated water would likely have been much more severely impacted. Treated water consistently provided elevated alkalinity and pH above that of the hatchery source water. (C) 2005 Elsevier B.V. All rights reserved.  
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  Notes (up) Limestone fluidized bed treatment of acid-impacted water at the Craig Brook National Fish Hatchery, Maine, USA; Wos:000235568800001; Times Cited: 0; ISI Web of Science Approved no  
  Call Number CBU @ c.wolke @ 16942 Serial 113  
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Author Lovell, H.L. url  openurl
  Title Limestone Treatment Of Coal Mine Drainage Type Journal Article
  Year 1971 Publication Min. Congr. J. Abbreviated Journal  
  Volume 57 Issue 10 Pages 28-&  
  Keywords mine water treatment  
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  ISSN 0026-5160 ISBN Medium  
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  Notes (up) Limestone Treatment Of Coal Mine Drainage; Wos:A1971k631900002; Times Cited: 1; J Allen Overton Jr, 1920 N St Nw, Washington, DC 20036; ISI Web of Science Approved no  
  Call Number CBU @ c.wolke @ 9263 Serial 101  
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Author Bamforth, S.M. url  openurl
  Title Manganese removal from mine waters – investigating the occurrence and importance of manganese carbonates Type Journal Article
  Year 2006 Publication Appl. Geochem. Abbreviated Journal  
  Volume 21 Issue 8 Pages 1274-1287  
  Keywords mine water treatment  
  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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  Notes (up) Manganese removal from mine waters – investigating the occurrence and importance of manganese carbonates; Wos:000240297600004; Times Cited: 0; ISI Web of Science Approved no  
  Call Number CBU @ c.wolke @ 16916 Serial 107  
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