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Destruction of organic pollutants in reusable wastewater using advanced oxidation technology
This work studied the destruction of various M–EDTA complexes and trace organic pollutants in treated reusable wastewater under advanced oxidation using UV irradiation and ozonation. Effect of dosage of hydrogen peroxide and acidity of reaction matrices on oxidation efficiencies were investigated. T...
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Published in: | Chemosphere (Oxford) 2005-04, Vol.59 (3), p.441-445 |
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container_end_page | 445 |
container_issue | 3 |
container_start_page | 441 |
container_title | Chemosphere (Oxford) |
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creator | Yang, C. Xu, Y.R. Teo, K.C. Goh, N.K. Chia, L.S. Xie, R.J. |
description | This work studied the destruction of various M–EDTA complexes and trace organic pollutants in treated reusable wastewater under advanced oxidation using UV irradiation and ozonation. Effect of dosage of hydrogen peroxide and acidity of reaction matrices on oxidation efficiencies were investigated. The rate constant of mineralization presents a decreasing trend as Fe(III)–EDTA
>
Fe(II)–EDTA
>
Al(III)–EDTA
>
Pb(II)–EDTA
>
Na(I)–EDTA
>
Zn(II)–EDTA
>
Cu(II)–EDTA. The mineralization efficiencies using ozone alone are 15%, 40% and 15% for the water samples after reverse osmosis (RO), microfiltration (MF) and superfiltration (SF) processes, respectively. The presence of hydrogen peroxide in photochemical reaction matrixes can effectively enhance the mineralization of organic carbon species. When 150
mg
l
−1 of H
2O
2 was added in the effluents, the mineralization markedly increased to 80%, 92% and 89%, respectively. |
doi_str_mv | 10.1016/j.chemosphere.2004.10.020 |
format | article |
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>
Fe(II)–EDTA
>
Al(III)–EDTA
>
Pb(II)–EDTA
>
Na(I)–EDTA
>
Zn(II)–EDTA
>
Cu(II)–EDTA. The mineralization efficiencies using ozone alone are 15%, 40% and 15% for the water samples after reverse osmosis (RO), microfiltration (MF) and superfiltration (SF) processes, respectively. The presence of hydrogen peroxide in photochemical reaction matrixes can effectively enhance the mineralization of organic carbon species. When 150
mg
l
−1 of H
2O
2 was added in the effluents, the mineralization markedly increased to 80%, 92% and 89%, respectively.</description><identifier>ISSN: 0045-6535</identifier><identifier>EISSN: 1879-1298</identifier><identifier>DOI: 10.1016/j.chemosphere.2004.10.020</identifier><identifier>PMID: 15763097</identifier><identifier>CODEN: CMSHAF</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Advanced oxidation technology ; Applied sciences ; Edetic Acid - chemistry ; Exact sciences and technology ; Hydrogen Peroxide - chemistry ; Kinetics ; Organic pollutants ; Oxidation-Reduction ; Ozone ; Ozone - chemistry ; Photochemistry - methods ; Pollution ; Ultraviolet ; Ultraviolet Rays ; Waste Disposal, Fluid - instrumentation ; Waste Disposal, Fluid - methods ; Wastewaters reuse. Miscellaneous ; Water ; Water Pollutants, Chemical ; Water treatment and pollution</subject><ispartof>Chemosphere (Oxford), 2005-04, Vol.59 (3), p.441-445</ispartof><rights>2004 Elsevier Ltd</rights><rights>2005 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c467t-706f5002ad3efcfd422f3bcb2497156985f5c7f1e014487de8684142bef639153</citedby><cites>FETCH-LOGICAL-c467t-706f5002ad3efcfd422f3bcb2497156985f5c7f1e014487de8684142bef639153</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16695564$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15763097$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yang, C.</creatorcontrib><creatorcontrib>Xu, Y.R.</creatorcontrib><creatorcontrib>Teo, K.C.</creatorcontrib><creatorcontrib>Goh, N.K.</creatorcontrib><creatorcontrib>Chia, L.S.</creatorcontrib><creatorcontrib>Xie, R.J.</creatorcontrib><title>Destruction of organic pollutants in reusable wastewater using advanced oxidation technology</title><title>Chemosphere (Oxford)</title><addtitle>Chemosphere</addtitle><description>This work studied the destruction of various M–EDTA complexes and trace organic pollutants in treated reusable wastewater under advanced oxidation using UV irradiation and ozonation. Effect of dosage of hydrogen peroxide and acidity of reaction matrices on oxidation efficiencies were investigated. The rate constant of mineralization presents a decreasing trend as Fe(III)–EDTA
>
Fe(II)–EDTA
>
Al(III)–EDTA
>
Pb(II)–EDTA
>
Na(I)–EDTA
>
Zn(II)–EDTA
>
Cu(II)–EDTA. The mineralization efficiencies using ozone alone are 15%, 40% and 15% for the water samples after reverse osmosis (RO), microfiltration (MF) and superfiltration (SF) processes, respectively. The presence of hydrogen peroxide in photochemical reaction matrixes can effectively enhance the mineralization of organic carbon species. When 150
mg
l
−1 of H
2O
2 was added in the effluents, the mineralization markedly increased to 80%, 92% and 89%, respectively.</description><subject>Advanced oxidation technology</subject><subject>Applied sciences</subject><subject>Edetic Acid - chemistry</subject><subject>Exact sciences and technology</subject><subject>Hydrogen Peroxide - chemistry</subject><subject>Kinetics</subject><subject>Organic pollutants</subject><subject>Oxidation-Reduction</subject><subject>Ozone</subject><subject>Ozone - chemistry</subject><subject>Photochemistry - methods</subject><subject>Pollution</subject><subject>Ultraviolet</subject><subject>Ultraviolet Rays</subject><subject>Waste Disposal, Fluid - instrumentation</subject><subject>Waste Disposal, Fluid - methods</subject><subject>Wastewaters reuse. Miscellaneous</subject><subject>Water</subject><subject>Water Pollutants, Chemical</subject><subject>Water treatment and pollution</subject><issn>0045-6535</issn><issn>1879-1298</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNqNkUtvEzEUhS0EoqHwF5BZwG6C3x4vUXhKldjADsnyeK4TR5NxsD0t_fc4JFLZwcqS73fu4xyEXlGypoSqt_u138EhleMOMqwZIaL9rwkjj9CK9tp0lJn-MVq1guyU5PIKPStlT0gTS_MUXVGpFSdGr9CP91BqXnyNacYp4JS3bo4eH9M0LdXNteA44wxLccME-M6VCneuQsZLifMWu_HWzR5GnH7F0f3pUsHv5jSl7f1z9CS4qcCLy3uNvn_88G3zubv5-unL5t1N54XStdNEBUkIcyOH4MMoGAt88AMTRlOpTC-D9DpQIFSIXo_Qq15QwQYIihsq-TV6c-57zOnn0g6yh1g8TJObIS3FUkUN15z9GxSayzaxgeYM-pxKyRDsMceDy_eWEnvKwO7tXxnYUwanUsugaV9ehizDAcYH5cX0Bry-AK54N4XcHIzlgVPKtCVE4zZnDpp3txGyLT7Cye2YwVc7pvgf6_wGXGusbA</recordid><startdate>20050401</startdate><enddate>20050401</enddate><creator>Yang, C.</creator><creator>Xu, Y.R.</creator><creator>Teo, K.C.</creator><creator>Goh, N.K.</creator><creator>Chia, L.S.</creator><creator>Xie, R.J.</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>7ST</scope><scope>C1K</scope><scope>SOI</scope><scope>7QH</scope><scope>7TV</scope><scope>7UA</scope></search><sort><creationdate>20050401</creationdate><title>Destruction of organic pollutants in reusable wastewater using advanced oxidation technology</title><author>Yang, C. ; Xu, Y.R. ; Teo, K.C. ; Goh, N.K. ; Chia, L.S. ; Xie, R.J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c467t-706f5002ad3efcfd422f3bcb2497156985f5c7f1e014487de8684142bef639153</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Advanced oxidation technology</topic><topic>Applied sciences</topic><topic>Edetic Acid - chemistry</topic><topic>Exact sciences and technology</topic><topic>Hydrogen Peroxide - chemistry</topic><topic>Kinetics</topic><topic>Organic pollutants</topic><topic>Oxidation-Reduction</topic><topic>Ozone</topic><topic>Ozone - chemistry</topic><topic>Photochemistry - methods</topic><topic>Pollution</topic><topic>Ultraviolet</topic><topic>Ultraviolet Rays</topic><topic>Waste Disposal, Fluid - instrumentation</topic><topic>Waste Disposal, Fluid - methods</topic><topic>Wastewaters reuse. Miscellaneous</topic><topic>Water</topic><topic>Water Pollutants, Chemical</topic><topic>Water treatment and pollution</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yang, C.</creatorcontrib><creatorcontrib>Xu, Y.R.</creatorcontrib><creatorcontrib>Teo, K.C.</creatorcontrib><creatorcontrib>Goh, N.K.</creatorcontrib><creatorcontrib>Chia, L.S.</creatorcontrib><creatorcontrib>Xie, R.J.</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>Environment Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Environment Abstracts</collection><collection>Aqualine</collection><collection>Pollution Abstracts</collection><collection>Water Resources Abstracts</collection><jtitle>Chemosphere (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yang, C.</au><au>Xu, Y.R.</au><au>Teo, K.C.</au><au>Goh, N.K.</au><au>Chia, L.S.</au><au>Xie, R.J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Destruction of organic pollutants in reusable wastewater using advanced oxidation technology</atitle><jtitle>Chemosphere (Oxford)</jtitle><addtitle>Chemosphere</addtitle><date>2005-04-01</date><risdate>2005</risdate><volume>59</volume><issue>3</issue><spage>441</spage><epage>445</epage><pages>441-445</pages><issn>0045-6535</issn><eissn>1879-1298</eissn><coden>CMSHAF</coden><abstract>This work studied the destruction of various M–EDTA complexes and trace organic pollutants in treated reusable wastewater under advanced oxidation using UV irradiation and ozonation. Effect of dosage of hydrogen peroxide and acidity of reaction matrices on oxidation efficiencies were investigated. The rate constant of mineralization presents a decreasing trend as Fe(III)–EDTA
>
Fe(II)–EDTA
>
Al(III)–EDTA
>
Pb(II)–EDTA
>
Na(I)–EDTA
>
Zn(II)–EDTA
>
Cu(II)–EDTA. The mineralization efficiencies using ozone alone are 15%, 40% and 15% for the water samples after reverse osmosis (RO), microfiltration (MF) and superfiltration (SF) processes, respectively. The presence of hydrogen peroxide in photochemical reaction matrixes can effectively enhance the mineralization of organic carbon species. When 150
mg
l
−1 of H
2O
2 was added in the effluents, the mineralization markedly increased to 80%, 92% and 89%, respectively.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><pmid>15763097</pmid><doi>10.1016/j.chemosphere.2004.10.020</doi><tpages>5</tpages></addata></record> |
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subjects | Advanced oxidation technology Applied sciences Edetic Acid - chemistry Exact sciences and technology Hydrogen Peroxide - chemistry Kinetics Organic pollutants Oxidation-Reduction Ozone Ozone - chemistry Photochemistry - methods Pollution Ultraviolet Ultraviolet Rays Waste Disposal, Fluid - instrumentation Waste Disposal, Fluid - methods Wastewaters reuse. Miscellaneous Water Water Pollutants, Chemical Water treatment and pollution |
title | Destruction of organic pollutants in reusable wastewater using advanced oxidation technology |
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