Effects of various ions on the dechlorination kinetics of hexachlorobenzene by nanoscale zero-valent iron
► The degradation kinetics of HCB by NZVI is not affected by HCO3-, Mg2+, and Na+. ► Cl− and SO42- enhance the degradation reaction due to their corrosion promotion. ► NO3- competes with HCB so it inhibits the degradation reaction. ► Cu2+ enhances degradation of HCB resulted from the reduced form of...
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Veröffentlicht in: | Chemosphere (Oxford) 2012-09, Vol.88 (11), p.1346-1352 |
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description | ► The degradation kinetics of HCB by NZVI is not affected by HCO3-, Mg2+, and Na+. ► Cl− and SO42- enhance the degradation reaction due to their corrosion promotion. ► NO3- competes with HCB so it inhibits the degradation reaction. ► Cu2+ enhances degradation of HCB resulted from the reduced form of Cu on NZVI. ► Fe2+ inhibits the degradation reaction due to passivation layers formed.
The effect of several anions and cations normally co-present in soil and groundwater contamination sites on the degradation kinetics and removal efficiency of hexachlorobenzene (HCB) by nanoscale zero-valent iron (NZVI) particles was examined. The degradation kinetics was not influenced by the HCO3-, Mg2+, and Na+ ions. It was enhanced in the presence of the Cl− and SO42- ions due to their corrosion promotion. The NO3- competes with HCB so it inhibits the degradation reaction. The Fe2+ ions would inhibit the degradation reaction due to passivation layer formed, while it was enhanced in the presence of Cu2+ ions resulted from the reduced form of copper on NZVI surfaces. These observations lead to a better understanding of HCB dechlorination with NZVI particles and can facilitate the remediation design and prediction of treatment efficiency of HCB at remediation sites. |
doi_str_mv | 10.1016/j.chemosphere.2012.05.036 |
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The effect of several anions and cations normally co-present in soil and groundwater contamination sites on the degradation kinetics and removal efficiency of hexachlorobenzene (HCB) by nanoscale zero-valent iron (NZVI) particles was examined. The degradation kinetics was not influenced by the HCO3-, Mg2+, and Na+ ions. It was enhanced in the presence of the Cl− and SO42- ions due to their corrosion promotion. The NO3- competes with HCB so it inhibits the degradation reaction. The Fe2+ ions would inhibit the degradation reaction due to passivation layer formed, while it was enhanced in the presence of Cu2+ ions resulted from the reduced form of copper on NZVI surfaces. These observations lead to a better understanding of HCB dechlorination with NZVI particles and can facilitate the remediation design and prediction of treatment efficiency of HCB at remediation sites.</description><identifier>ISSN: 0045-6535</identifier><identifier>EISSN: 1879-1298</identifier><identifier>DOI: 10.1016/j.chemosphere.2012.05.036</identifier><identifier>PMID: 22704216</identifier><identifier>CODEN: CMSHAF</identifier><language>eng</language><publisher>Kidlington: Elsevier Ltd</publisher><subject>Anions ; Applied sciences ; Cations ; Dechlorination ; Decontamination. Miscellaneous ; Degradation ; Earth sciences ; Earth, ocean, space ; Engineering and environment geology. Geothermics ; Exact sciences and technology ; Groundwaters ; Hexachlorobenzene ; Hexachlorobenzene (HCB) ; Hexachlorobenzene - chemistry ; Ions - chemistry ; Iron ; Iron - chemistry ; Kinetics ; Nanocomposites ; Nanomaterials ; Nanoscale zero-valent iron (NZVI) ; Nanostructure ; Natural water pollution ; Pollution ; Pollution, environment geology ; Remediation ; Soil and sediments pollution ; Water treatment and pollution</subject><ispartof>Chemosphere (Oxford), 2012-09, Vol.88 (11), p.1346-1352</ispartof><rights>2012 Elsevier Ltd</rights><rights>2014 INIST-CNRS</rights><rights>Copyright © 2012 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c473t-7af0766499cfe68c5a5e8e2394082209d0c3ecbac3313047ba1242da7f58d4e53</citedby><cites>FETCH-LOGICAL-c473t-7af0766499cfe68c5a5e8e2394082209d0c3ecbac3313047ba1242da7f58d4e53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.chemosphere.2012.05.036$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27922,27923,45993</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=26127868$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22704216$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Su, Yuh-fan</creatorcontrib><creatorcontrib>Hsu, Chung-Yu</creatorcontrib><creatorcontrib>Shih, Yang-hsin</creatorcontrib><title>Effects of various ions on the dechlorination kinetics of hexachlorobenzene by nanoscale zero-valent iron</title><title>Chemosphere (Oxford)</title><addtitle>Chemosphere</addtitle><description>► The degradation kinetics of HCB by NZVI is not affected by HCO3-, Mg2+, and Na+. ► Cl− and SO42- enhance the degradation reaction due to their corrosion promotion. ► NO3- competes with HCB so it inhibits the degradation reaction. ► Cu2+ enhances degradation of HCB resulted from the reduced form of Cu on NZVI. ► Fe2+ inhibits the degradation reaction due to passivation layers formed.
The effect of several anions and cations normally co-present in soil and groundwater contamination sites on the degradation kinetics and removal efficiency of hexachlorobenzene (HCB) by nanoscale zero-valent iron (NZVI) particles was examined. The degradation kinetics was not influenced by the HCO3-, Mg2+, and Na+ ions. It was enhanced in the presence of the Cl− and SO42- ions due to their corrosion promotion. The NO3- competes with HCB so it inhibits the degradation reaction. The Fe2+ ions would inhibit the degradation reaction due to passivation layer formed, while it was enhanced in the presence of Cu2+ ions resulted from the reduced form of copper on NZVI surfaces. These observations lead to a better understanding of HCB dechlorination with NZVI particles and can facilitate the remediation design and prediction of treatment efficiency of HCB at remediation sites.</description><subject>Anions</subject><subject>Applied sciences</subject><subject>Cations</subject><subject>Dechlorination</subject><subject>Decontamination. Miscellaneous</subject><subject>Degradation</subject><subject>Earth sciences</subject><subject>Earth, ocean, space</subject><subject>Engineering and environment geology. Geothermics</subject><subject>Exact sciences and technology</subject><subject>Groundwaters</subject><subject>Hexachlorobenzene</subject><subject>Hexachlorobenzene (HCB)</subject><subject>Hexachlorobenzene - chemistry</subject><subject>Ions - chemistry</subject><subject>Iron</subject><subject>Iron - chemistry</subject><subject>Kinetics</subject><subject>Nanocomposites</subject><subject>Nanomaterials</subject><subject>Nanoscale zero-valent iron (NZVI)</subject><subject>Nanostructure</subject><subject>Natural water pollution</subject><subject>Pollution</subject><subject>Pollution, environment geology</subject><subject>Remediation</subject><subject>Soil and sediments pollution</subject><subject>Water treatment and pollution</subject><issn>0045-6535</issn><issn>1879-1298</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkUtv1DAUhS1ERaeFv4DMAolNUr_jLNGoQKVKbNq15Tg3ioeMPdiZEe2vx-kMj-Ws_PrOvdfnIPSBkpoSqm42tRthG_NuhAQ1I5TVRNaEq1doRXXTVpS1-jVaESJkpSSXl-gq5w0hRSzbN-iSsYYIRtUK-dthADdnHAd8sMnHfcY-hnIOeB4B9-DGKSYf7Fyu8Q8fYPbuBR_hl315jB2EZwiAuyccbIjZ2QnwM6RYHcouzNinGN6ii8FOGd6d1mv0-OX2Yf2tuv_-9W79-b5youFz1diBNEqJtnUDKO2klaCB8VYQzRhpe-I4uM46ziknouksZYL1thmk7gVIfo0-HevuUvy5hzybrc8OpskGKL8zxQIqKBXNGSjhmhPGqD4DZbyYzvRStT2iLsWcEwxml_zWpqcCmSU_szH_5WeW_AyRpuRXtO9PbfbdFvq_yj-BFeDjCbCLzUOywfn8j1OUNVot866PHBSrDx6Syc5DcND7VPI2ffRnjPMbCBe_bA</recordid><startdate>20120901</startdate><enddate>20120901</enddate><creator>Su, Yuh-fan</creator><creator>Hsu, Chung-Yu</creator><creator>Shih, Yang-hsin</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7QH</scope><scope>7TV</scope><scope>7UA</scope><scope>C1K</scope><scope>F1W</scope><scope>H97</scope><scope>L.G</scope><scope>7SE</scope><scope>8FD</scope><scope>FR3</scope><scope>JG9</scope><scope>KR7</scope></search><sort><creationdate>20120901</creationdate><title>Effects of various ions on the dechlorination kinetics of hexachlorobenzene by nanoscale zero-valent iron</title><author>Su, Yuh-fan ; Hsu, Chung-Yu ; Shih, Yang-hsin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c473t-7af0766499cfe68c5a5e8e2394082209d0c3ecbac3313047ba1242da7f58d4e53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Anions</topic><topic>Applied sciences</topic><topic>Cations</topic><topic>Dechlorination</topic><topic>Decontamination. Miscellaneous</topic><topic>Degradation</topic><topic>Earth sciences</topic><topic>Earth, ocean, space</topic><topic>Engineering and environment geology. Geothermics</topic><topic>Exact sciences and technology</topic><topic>Groundwaters</topic><topic>Hexachlorobenzene</topic><topic>Hexachlorobenzene (HCB)</topic><topic>Hexachlorobenzene - chemistry</topic><topic>Ions - chemistry</topic><topic>Iron</topic><topic>Iron - chemistry</topic><topic>Kinetics</topic><topic>Nanocomposites</topic><topic>Nanomaterials</topic><topic>Nanoscale zero-valent iron (NZVI)</topic><topic>Nanostructure</topic><topic>Natural water pollution</topic><topic>Pollution</topic><topic>Pollution, environment geology</topic><topic>Remediation</topic><topic>Soil and sediments pollution</topic><topic>Water treatment and pollution</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Su, Yuh-fan</creatorcontrib><creatorcontrib>Hsu, Chung-Yu</creatorcontrib><creatorcontrib>Shih, Yang-hsin</creatorcontrib><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>MEDLINE - Academic</collection><collection>Aqualine</collection><collection>Pollution Abstracts</collection><collection>Water Resources Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 3: Aquatic Pollution & Environmental Quality</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>Corrosion Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Materials Research Database</collection><collection>Civil Engineering Abstracts</collection><jtitle>Chemosphere (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Su, Yuh-fan</au><au>Hsu, Chung-Yu</au><au>Shih, Yang-hsin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of various ions on the dechlorination kinetics of hexachlorobenzene by nanoscale zero-valent iron</atitle><jtitle>Chemosphere (Oxford)</jtitle><addtitle>Chemosphere</addtitle><date>2012-09-01</date><risdate>2012</risdate><volume>88</volume><issue>11</issue><spage>1346</spage><epage>1352</epage><pages>1346-1352</pages><issn>0045-6535</issn><eissn>1879-1298</eissn><coden>CMSHAF</coden><abstract>► The degradation kinetics of HCB by NZVI is not affected by HCO3-, Mg2+, and Na+. ► Cl− and SO42- enhance the degradation reaction due to their corrosion promotion. ► NO3- competes with HCB so it inhibits the degradation reaction. ► Cu2+ enhances degradation of HCB resulted from the reduced form of Cu on NZVI. ► Fe2+ inhibits the degradation reaction due to passivation layers formed.
The effect of several anions and cations normally co-present in soil and groundwater contamination sites on the degradation kinetics and removal efficiency of hexachlorobenzene (HCB) by nanoscale zero-valent iron (NZVI) particles was examined. The degradation kinetics was not influenced by the HCO3-, Mg2+, and Na+ ions. It was enhanced in the presence of the Cl− and SO42- ions due to their corrosion promotion. The NO3- competes with HCB so it inhibits the degradation reaction. The Fe2+ ions would inhibit the degradation reaction due to passivation layer formed, while it was enhanced in the presence of Cu2+ ions resulted from the reduced form of copper on NZVI surfaces. These observations lead to a better understanding of HCB dechlorination with NZVI particles and can facilitate the remediation design and prediction of treatment efficiency of HCB at remediation sites.</abstract><cop>Kidlington</cop><pub>Elsevier Ltd</pub><pmid>22704216</pmid><doi>10.1016/j.chemosphere.2012.05.036</doi><tpages>7</tpages></addata></record> |
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subjects | Anions Applied sciences Cations Dechlorination Decontamination. Miscellaneous Degradation Earth sciences Earth, ocean, space Engineering and environment geology. Geothermics Exact sciences and technology Groundwaters Hexachlorobenzene Hexachlorobenzene (HCB) Hexachlorobenzene - chemistry Ions - chemistry Iron Iron - chemistry Kinetics Nanocomposites Nanomaterials Nanoscale zero-valent iron (NZVI) Nanostructure Natural water pollution Pollution Pollution, environment geology Remediation Soil and sediments pollution Water treatment and pollution |
title | Effects of various ions on the dechlorination kinetics of hexachlorobenzene by nanoscale zero-valent iron |
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