Publicação:
Comparison of oxidation efficiency of disperse dyes by chemical and photoelectrocatalytic chlorination and removal of mutagenic activity

dc.contributor.authorOsugi, Marly E. [UNESP]
dc.contributor.authorRajeshwar, Krishnan
dc.contributor.authorFerraz, Elisa R. A.
dc.contributor.authorde Oliveira, Danielle P.
dc.contributor.authorAraújo, Angela Regina [UNESP]
dc.contributor.authorZanoni, Maria Valnice Boldrin [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionUniv Texas Arlington
dc.date.accessioned2014-05-20T14:19:18Z
dc.date.available2014-05-20T14:19:18Z
dc.date.issued2009-02-28
dc.description.abstractDegradation of Disperse Orange 1, Disperse Red 1 and Disperse Red 13 dyes has been performed using electrochemical oxidation on Pt electrode, chemical chlorination and photoelectrochemical oxidation on Ti/TiO(2) thin film electrodes in NaCl or Na(2)SO(4) medium. 100% discoloration was obtained for all tested methods after 1 h of treatment. Faster color removal was obtained by photoelectrocatalytic oxidation in 0.1 mol L(-1) NaCl pH 4.0 under UV light and an applied potential of +1.0V (vs SCE reference electrode), which indicates also values around 60% of TOC removal. The conventional chlorination method and electrochemical oxidation on Pt electrode resulted in negligible reduction of TOC removal. All dyes showed positive mutagenic activity in the Salmonella/microsome assay with the strain TA98 in the absence and presence of S9 (exogenous metabolic activation). Nevertheless, there is complete reduction of the mutagenic activity after 1 h of photoelectrocatalytic oxidation, suggesting that this process would be good option to remove disperse azo dyes from aqueous media. (C) 2008 Elsevier Ltd. All rights reserved.en
dc.description.affiliationUNESP, Inst Quim, BR-14800900 Araraquara, SP, Brazil
dc.description.affiliationUniv São Paulo, Fac Ciencias Farmaceut Ribeirao Preto, BR-14040903 Ribeirao Preto, SP, Brazil
dc.description.affiliationUniv Texas Arlington, Ctr Renewable Energy Sci & Technol, Dept Chem & Biochem, Arlington, TX 76019 USA
dc.description.affiliationUnespUNESP, Inst Quim, BR-14800900 Araraquara, SP, Brazil
dc.format.extent2086-2093
dc.identifierhttp://dx.doi.org/10.1016/j.electacta.2008.07.015
dc.identifier.citationElectrochimica Acta. Oxford: Pergamon-Elsevier B.V. Ltd, v. 54, n. 7, p. 2086-2093, 2009.
dc.identifier.doi10.1016/j.electacta.2008.07.015
dc.identifier.issn0013-4686
dc.identifier.lattes0037579054083160
dc.identifier.orcid0000-0002-2296-1393
dc.identifier.orcid0000-0001-7616-9652
dc.identifier.urihttp://hdl.handle.net/11449/25825
dc.identifier.wosWOS:000264925100025
dc.language.isoeng
dc.publisherPergamon-Elsevier B.V. Ltd
dc.relation.ispartofElectrochimica Acta
dc.relation.ispartofjcr5.116
dc.relation.ispartofsjr1,439
dc.rights.accessRightsAcesso restrito
dc.sourceWeb of Science
dc.subjectActive chlorineen
dc.subjectDisperse azo dyeen
dc.subjectPhotoelectrocatalytic oxidationen
dc.subjectMutagenic activityen
dc.subjectTi/TiO(2) electrodesen
dc.titleComparison of oxidation efficiency of disperse dyes by chemical and photoelectrocatalytic chlorination and removal of mutagenic activityen
dc.typeArtigo
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderPergamon-Elsevier B.V. Ltd
dspace.entity.typePublication
unesp.author.lattes0037579054083160[5]
unesp.author.orcid0000-0001-7616-9652[5]
unesp.author.orcid0000-0002-2296-1393[6]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Química, Araraquarapt
unesp.departmentQuímica Analítica - IQARpt

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