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Chemical Changes in Sediment Pore-Waters of an Acidic Mining Lake After Addition of Organic Substrate and Lime for Stimulating Lake Remediation
Authors:P Herzsprung  K Friese  R Frömmichen  J Göttlicher  M Koschorreck  W V Tümpling Jr  K Wendt-Potthoff
Institution:(1) Department for Inland Water Research, UFZ-Centre for Environmental Research Leipzig-Halle Ltd., Brückstr. 3a, D-39114 Magdeburg, Germany;(2) UFOP-Universidade Federal de Ouro Preto, Campus Universitario, CEP 35.400-000 Ouro Preto, MG, Brazil;(3) Forschungszentrum Karlsruhe ITC-WGT, Hermann-von-Helmholtz-Platz 1, D-76344 Eggenstein-Leopoldshafen, Germany
Abstract:In the past five years, enclosures have beeninstalled in an acidic mining lake in Lusatia to investigate insitu remediation processes. They were treated with straw, withstraw and Carbokalk, or with Carbokalk alone, where Carbokalkis a by-product of the sugar industry (solid precipitate ofnon-sugars after lime clarification of extracted sugar beetjuice). Sediment samples were taken as cores to get informationabout the behaviour of organic and inorganic components insediment pore-water with depth. Vertical distributions of pH,soluble reactive phosphate, nitrate, ammonium, silica,aluminium, iron, manganese, calcium, magnesium, sodium,potassium, sulphate, and DOC were measured. The resultingprofiles, each consisting of 15 data points at differentdepths, were compared by cluster analysis. The similarities ofsediment cores from different treated enclosures relating toprofiles of chemical components were discussed. Increasedconcentrations of potassium and sulphate were found in pore-water after substrate treatment. The data imply dissolution ofpotassium iron sulphate hydroxide minerals (jarosite) after anincrease of pH caused by dissolution of lime and by sulphatereducing processes which were stimulated by organic substrateaddition.
Keywords:acidic mining lakes  cluster analysis  jarositedissolution  in situ remediation  sediment pore-water chemistry
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