In Situ Cr(VI) Reduction within Coarse-Textured, Oxide-Coated Soil and Aquifer Systems Using Fe(II) Solutions

Batch and column techniques were used to evaluate the in situ Cr(VI) reduction and immobilization using Fe(II) solutions within the sediments of the Atlantic Coastal Plain. Remediation treatments included Cr-free groundwater and buffered and unbuffered Fe(II) solutions as either FeCl2 and FeSO4. The...

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Veröffentlicht in:Environmental Science and Technology 1999-03, Vol.33 (6), p.938-944
Hauptverfasser: Seaman, John C, Bertsch, Paul M, Schwallie, L
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Bertsch, Paul M
Schwallie, L
description Batch and column techniques were used to evaluate the in situ Cr(VI) reduction and immobilization using Fe(II) solutions within the sediments of the Atlantic Coastal Plain. Remediation treatments included Cr-free groundwater and buffered and unbuffered Fe(II) solutions as either FeCl2 and FeSO4. The slow release of Cr(VI) from the Fe-oxide rich subsurface sediment following exposure to Cr-free solutions indicated that simple pump-and-treat procedures would require extended operation time to meet regulatory standards. In situ reduction was confirmed by the loss of Cr(VI) and Fe(II) from solution and a drop in pH compared to control systems. Batch and column-effluent Cr(VI) decreased with increasing Fe(II), generally falling below detection limits as the persistence of Fe(II) occurred. However, CrDissolved, presumably Cr(III), exceeded regulatory limits due to the low pH (≈3.0) induced by oxidation and hydrolysis of Fe(II). Acetate-buffered Fe(II) solutions maintained an elevated pH in the presence of Cr(VI) reduction, making the treatment effective at lowering CrDissolved in batch evaluations. Acetate increased Cr(VI) mobility in columns ahead of the reactive Fe(II) front, suggesting that in situ reduction using soluble chemical additives may be somewhat ineffective due to the enhanced migration of Cr, either Cr(III) or Cr(VI), induced by the treatment solution.
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Remediation treatments included Cr-free groundwater and buffered and unbuffered Fe(II) solutions as either FeCl2 and FeSO4. The slow release of Cr(VI) from the Fe-oxide rich subsurface sediment following exposure to Cr-free solutions indicated that simple pump-and-treat procedures would require extended operation time to meet regulatory standards. In situ reduction was confirmed by the loss of Cr(VI) and Fe(II) from solution and a drop in pH compared to control systems. Batch and column-effluent Cr(VI) decreased with increasing Fe(II), generally falling below detection limits as the persistence of Fe(II) occurred. However, CrDissolved, presumably Cr(III), exceeded regulatory limits due to the low pH (≈3.0) induced by oxidation and hydrolysis of Fe(II). Acetate-buffered Fe(II) solutions maintained an elevated pH in the presence of Cr(VI) reduction, making the treatment effective at lowering CrDissolved in batch evaluations. Acetate increased Cr(VI) mobility in columns ahead of the reactive Fe(II) front, suggesting that in situ reduction using soluble chemical additives may be somewhat ineffective due to the enhanced migration of Cr, either Cr(III) or Cr(VI), induced by the treatment solution.</description><identifier>ISSN: 0013-936X</identifier><identifier>EISSN: 1520-5851</identifier><identifier>DOI: 10.1021/es980546+</identifier><identifier>CODEN: ESTHAG</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>AGUAS SUBTERRANEAS ; Applied sciences ; AQUIFERS ; CAROLINA DEL SUR ; CAROLINE DU SUD ; CATION ; CATIONES ; CATIONS ; CHROME ; CHROMIUM ; COASTAL PLAINS ; CONTAMINANTES ; CROMO ; Decontamination. Miscellaneous ; Earth sciences ; Earth, ocean, space ; EAU SOUTERRAINE ; Engineering and environment geology. 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Sci. Technol</addtitle><description>Batch and column techniques were used to evaluate the in situ Cr(VI) reduction and immobilization using Fe(II) solutions within the sediments of the Atlantic Coastal Plain. Remediation treatments included Cr-free groundwater and buffered and unbuffered Fe(II) solutions as either FeCl2 and FeSO4. The slow release of Cr(VI) from the Fe-oxide rich subsurface sediment following exposure to Cr-free solutions indicated that simple pump-and-treat procedures would require extended operation time to meet regulatory standards. In situ reduction was confirmed by the loss of Cr(VI) and Fe(II) from solution and a drop in pH compared to control systems. Batch and column-effluent Cr(VI) decreased with increasing Fe(II), generally falling below detection limits as the persistence of Fe(II) occurred. However, CrDissolved, presumably Cr(III), exceeded regulatory limits due to the low pH (≈3.0) induced by oxidation and hydrolysis of Fe(II). 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Geothermics</topic><topic>ENVIRONMENTAL SCIENCES</topic><topic>Exact sciences and technology</topic><topic>FER</topic><topic>GROUND WATER</topic><topic>GROUNDWATER</topic><topic>GROUNDWATER POLLUTION</topic><topic>GROUNDWATER REMEDIATION</topic><topic>Groundwaters</topic><topic>HEXAVALENT CHROMIUM</topic><topic>HIERRO</topic><topic>IN-SITU PROCESSING</topic><topic>IRON</topic><topic>LLANURA COSTERA</topic><topic>METAL</topic><topic>METALES</topic><topic>METALS</topic><topic>Natural water pollution</topic><topic>PLAINE COTIERE</topic><topic>POLLUANT</topic><topic>POLLUTANTS</topic><topic>Pollution</topic><topic>POLLUTION DE L'EAU SOUTERRAINE</topic><topic>Pollution, environment geology</topic><topic>POLUCION DE AGUAS SUBTERRANEAS</topic><topic>REMEDIAL ACTION</topic><topic>SEDIMENT</topic><topic>SEDIMENTO</topic><topic>Soil and sediments pollution</topic><topic>SOIL CHEMISTRY</topic><topic>SOILS</topic><topic>SOUTH CAROLINA</topic><topic>Water treatment</topic><topic>Water treatment and pollution</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Seaman, John C</creatorcontrib><creatorcontrib>Bertsch, Paul M</creatorcontrib><creatorcontrib>Schwallie, L</creatorcontrib><collection>AGRIS</collection><collection>Istex</collection><collection>Pascal-Francis</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>Aqualine</collection><collection>Water Resources Abstracts</collection><collection>OSTI.GOV</collection><jtitle>Environmental Science and Technology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Seaman, John C</au><au>Bertsch, Paul M</au><au>Schwallie, L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>In Situ Cr(VI) Reduction within Coarse-Textured, Oxide-Coated Soil and Aquifer Systems Using Fe(II) Solutions</atitle><jtitle>Environmental Science and Technology</jtitle><addtitle>Environ. Sci. Technol</addtitle><date>1999-03-15</date><risdate>1999</risdate><volume>33</volume><issue>6</issue><spage>938</spage><epage>944</epage><pages>938-944</pages><issn>0013-936X</issn><eissn>1520-5851</eissn><coden>ESTHAG</coden><abstract>Batch and column techniques were used to evaluate the in situ Cr(VI) reduction and immobilization using Fe(II) solutions within the sediments of the Atlantic Coastal Plain. Remediation treatments included Cr-free groundwater and buffered and unbuffered Fe(II) solutions as either FeCl2 and FeSO4. The slow release of Cr(VI) from the Fe-oxide rich subsurface sediment following exposure to Cr-free solutions indicated that simple pump-and-treat procedures would require extended operation time to meet regulatory standards. In situ reduction was confirmed by the loss of Cr(VI) and Fe(II) from solution and a drop in pH compared to control systems. Batch and column-effluent Cr(VI) decreased with increasing Fe(II), generally falling below detection limits as the persistence of Fe(II) occurred. However, CrDissolved, presumably Cr(III), exceeded regulatory limits due to the low pH (≈3.0) induced by oxidation and hydrolysis of Fe(II). Acetate-buffered Fe(II) solutions maintained an elevated pH in the presence of Cr(VI) reduction, making the treatment effective at lowering CrDissolved in batch evaluations. Acetate increased Cr(VI) mobility in columns ahead of the reactive Fe(II) front, suggesting that in situ reduction using soluble chemical additives may be somewhat ineffective due to the enhanced migration of Cr, either Cr(III) or Cr(VI), induced by the treatment solution.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><doi>10.1021/es980546+</doi><tpages>7</tpages></addata></record>
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ispartof Environmental Science and Technology, 1999-03, Vol.33 (6), p.938-944
issn 0013-936X
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source American Chemical Society Journals
subjects AGUAS SUBTERRANEAS
Applied sciences
AQUIFERS
CAROLINA DEL SUR
CAROLINE DU SUD
CATION
CATIONES
CATIONS
CHROME
CHROMIUM
COASTAL PLAINS
CONTAMINANTES
CROMO
Decontamination. Miscellaneous
Earth sciences
Earth, ocean, space
EAU SOUTERRAINE
Engineering and environment geology. Geothermics
ENVIRONMENTAL SCIENCES
Exact sciences and technology
FER
GROUND WATER
GROUNDWATER
GROUNDWATER POLLUTION
GROUNDWATER REMEDIATION
Groundwaters
HEXAVALENT CHROMIUM
HIERRO
IN-SITU PROCESSING
IRON
LLANURA COSTERA
METAL
METALES
METALS
Natural water pollution
PLAINE COTIERE
POLLUANT
POLLUTANTS
Pollution
POLLUTION DE L'EAU SOUTERRAINE
Pollution, environment geology
POLUCION DE AGUAS SUBTERRANEAS
REMEDIAL ACTION
SEDIMENT
SEDIMENTO
Soil and sediments pollution
SOIL CHEMISTRY
SOILS
SOUTH CAROLINA
Water treatment
Water treatment and pollution
title In Situ Cr(VI) Reduction within Coarse-Textured, Oxide-Coated Soil and Aquifer Systems Using Fe(II) Solutions
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