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Reductive Dechlorination of Tetrachloroethylene and Trichloroethylene by Mackinawite (FeS) in the Presence of Metals: Reaction Rates
Reductive dechlorination by mackinawite (FeS) is an important transformation pathway for chloroethylenes in anoxic environments. Yet, the impact of metals on reductive dechlorination is not well understood, despite their frequent cooccurrence with chloroethylenes. Fe(II), Co(II), Ni(II), and Hg(II)...
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Published in: | Environmental science & technology 2007-09, Vol.41 (18), p.6390-6396 |
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description | Reductive dechlorination by mackinawite (FeS) is an important transformation pathway for chloroethylenes in anoxic environments. Yet, the impact of metals on reductive dechlorination is not well understood, despite their frequent cooccurrence with chloroethylenes. Fe(II), Co(II), Ni(II), and Hg(II) were evaluated for their impact on the dechlorination rates of PCE and TCE by FeS. Compared with unamended FeS batches, the dechlorination rates of both chloroethylenes decreased by addition of 0.01 M Fe(II). Relative to 0.01 M Fe(II)-added FeS batches, the dechlorination rates increased in FeS batches amended with 0.01 M of Co(II) and Hg(II), whereas the rates decreased in 0.01 M Ni(II)-added batches. While significantly impacting the dechlorination rates, the amended metals were quantitatively sequestered by FeS mainly because of formation of metal sulfides. Comparison of the dechlorination rates between metal-added FeS batches and metal sulfide batches suggests that discrete metal sulfides do not form in metal-added FeS batches. The observed exceptionally high reactivity of CoS suggests that it may be useful in reactive permeable barrier applications because of its stability in anoxic waters. The dechlorination rates of PCE and TCE significantly varied with Fe(II) amendment concentrations (Fe(II)0), indicating the presence of different types of solid-bound Fe phases with Fe(II)0. |
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Yet, the impact of metals on reductive dechlorination is not well understood, despite their frequent cooccurrence with chloroethylenes. Fe(II), Co(II), Ni(II), and Hg(II) were evaluated for their impact on the dechlorination rates of PCE and TCE by FeS. Compared with unamended FeS batches, the dechlorination rates of both chloroethylenes decreased by addition of 0.01 M Fe(II). Relative to 0.01 M Fe(II)-added FeS batches, the dechlorination rates increased in FeS batches amended with 0.01 M of Co(II) and Hg(II), whereas the rates decreased in 0.01 M Ni(II)-added batches. While significantly impacting the dechlorination rates, the amended metals were quantitatively sequestered by FeS mainly because of formation of metal sulfides. Comparison of the dechlorination rates between metal-added FeS batches and metal sulfide batches suggests that discrete metal sulfides do not form in metal-added FeS batches. The observed exceptionally high reactivity of CoS suggests that it may be useful in reactive permeable barrier applications because of its stability in anoxic waters. The dechlorination rates of PCE and TCE significantly varied with Fe(II) amendment concentrations (Fe(II)0), indicating the presence of different types of solid-bound Fe phases with Fe(II)0.</description><identifier>ISSN: 0013-936X</identifier><identifier>EISSN: 1520-5851</identifier><identifier>DOI: 10.1021/es0706394</identifier><identifier>PMID: 17948784</identifier><identifier>CODEN: ESTHAG</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Applied sciences ; Catalysis ; Chemical reactions ; Earth sciences ; Earth, ocean, space ; Engineering and environment geology. 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Sci. Technol</addtitle><description>Reductive dechlorination by mackinawite (FeS) is an important transformation pathway for chloroethylenes in anoxic environments. Yet, the impact of metals on reductive dechlorination is not well understood, despite their frequent cooccurrence with chloroethylenes. Fe(II), Co(II), Ni(II), and Hg(II) were evaluated for their impact on the dechlorination rates of PCE and TCE by FeS. Compared with unamended FeS batches, the dechlorination rates of both chloroethylenes decreased by addition of 0.01 M Fe(II). Relative to 0.01 M Fe(II)-added FeS batches, the dechlorination rates increased in FeS batches amended with 0.01 M of Co(II) and Hg(II), whereas the rates decreased in 0.01 M Ni(II)-added batches. While significantly impacting the dechlorination rates, the amended metals were quantitatively sequestered by FeS mainly because of formation of metal sulfides. Comparison of the dechlorination rates between metal-added FeS batches and metal sulfide batches suggests that discrete metal sulfides do not form in metal-added FeS batches. The observed exceptionally high reactivity of CoS suggests that it may be useful in reactive permeable barrier applications because of its stability in anoxic waters. The dechlorination rates of PCE and TCE significantly varied with Fe(II) amendment concentrations (Fe(II)0), indicating the presence of different types of solid-bound Fe phases with Fe(II)0.</description><subject>Applied sciences</subject><subject>Catalysis</subject><subject>Chemical reactions</subject><subject>Earth sciences</subject><subject>Earth, ocean, space</subject><subject>Engineering and environment geology. 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Geothermics</topic><topic>Environmental science</topic><topic>Exact sciences and technology</topic><topic>Ferrous Compounds - chemistry</topic><topic>Groundwaters</topic><topic>Hydrocarbons, Chlorinated - chemistry</topic><topic>Kinetics</topic><topic>Metals</topic><topic>Metals - chemistry</topic><topic>Natural water pollution</topic><topic>Oxidation-Reduction</topic><topic>Pollution</topic><topic>Pollution, environment geology</topic><topic>Sulfide compounds</topic><topic>Tetrachloroethylene - chemistry</topic><topic>Trichloroethylene - chemistry</topic><topic>Water treatment and pollution</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jeong, Hoon Y</creatorcontrib><creatorcontrib>Hayes, Kim F</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Environment Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environment Abstracts</collection><collection>Pollution Abstracts</collection><jtitle>Environmental science & technology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jeong, Hoon Y</au><au>Hayes, Kim F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Reductive Dechlorination of Tetrachloroethylene and Trichloroethylene by Mackinawite (FeS) in the Presence of Metals: Reaction Rates</atitle><jtitle>Environmental science & technology</jtitle><addtitle>Environ. Sci. Technol</addtitle><date>2007-09-15</date><risdate>2007</risdate><volume>41</volume><issue>18</issue><spage>6390</spage><epage>6396</epage><pages>6390-6396</pages><issn>0013-936X</issn><eissn>1520-5851</eissn><coden>ESTHAG</coden><abstract>Reductive dechlorination by mackinawite (FeS) is an important transformation pathway for chloroethylenes in anoxic environments. Yet, the impact of metals on reductive dechlorination is not well understood, despite their frequent cooccurrence with chloroethylenes. Fe(II), Co(II), Ni(II), and Hg(II) were evaluated for their impact on the dechlorination rates of PCE and TCE by FeS. Compared with unamended FeS batches, the dechlorination rates of both chloroethylenes decreased by addition of 0.01 M Fe(II). Relative to 0.01 M Fe(II)-added FeS batches, the dechlorination rates increased in FeS batches amended with 0.01 M of Co(II) and Hg(II), whereas the rates decreased in 0.01 M Ni(II)-added batches. While significantly impacting the dechlorination rates, the amended metals were quantitatively sequestered by FeS mainly because of formation of metal sulfides. Comparison of the dechlorination rates between metal-added FeS batches and metal sulfide batches suggests that discrete metal sulfides do not form in metal-added FeS batches. The observed exceptionally high reactivity of CoS suggests that it may be useful in reactive permeable barrier applications because of its stability in anoxic waters. The dechlorination rates of PCE and TCE significantly varied with Fe(II) amendment concentrations (Fe(II)0), indicating the presence of different types of solid-bound Fe phases with Fe(II)0.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>17948784</pmid><doi>10.1021/es0706394</doi><tpages>7</tpages></addata></record> |
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subjects | Applied sciences Catalysis Chemical reactions Earth sciences Earth, ocean, space Engineering and environment geology. Geothermics Environmental science Exact sciences and technology Ferrous Compounds - chemistry Groundwaters Hydrocarbons, Chlorinated - chemistry Kinetics Metals Metals - chemistry Natural water pollution Oxidation-Reduction Pollution Pollution, environment geology Sulfide compounds Tetrachloroethylene - chemistry Trichloroethylene - chemistry Water treatment and pollution |
title | Reductive Dechlorination of Tetrachloroethylene and Trichloroethylene by Mackinawite (FeS) in the Presence of Metals: Reaction Rates |
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