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dc.contributor.authorLizier, Thiago M.-
dc.contributor.authorZanoni, Thalita Boldrin-
dc.contributor.authorde Oliveira, Danielle Palma-
dc.contributor.authorZanoni, Maria Valnice Boldrin-
dc.date.accessioned2014-05-20T14:18:57Z-
dc.date.accessioned2016-10-25T17:40:49Z-
dc.date.available2014-05-20T14:18:57Z-
dc.date.available2016-10-25T17:40:49Z-
dc.date.issued2012-09-01-
dc.identifierhttp://www.electrochemsci.org/papers/vol7/7097784.pdf-
dc.identifier.citationInternational Journal of Electrochemical Science. Belgrade: Electrochemical Science Group, v. 7, n. 9, p. 7784-7796, 2012.-
dc.identifier.issn1452-3981-
dc.identifier.urihttp://hdl.handle.net/11449/25710-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/25710-
dc.description.abstractThe present work describes the electrochemical reduction of the azo dye Sudan III in methanol/0.01 mol l(-1) Bu4NBF4 at applied potential of -1.2V, which promotes 98% discoloration of the commercial sample. The reduction products were analyzed by high performance liquid chromatography, after optimized conditions for 20 aromatic amines with carcinogenic potentiality. The harmful compounds such as: aniline, benzidine, o-toluidine, 2,6-dimethylaniline, 4,4'-oxydianiline, 4,4'-metileno-bis-2-methylaniline and 4-aminobiphenyl are formed after azo bond cleavage. The electrochemical reduction is compared with chemical reduction by using sodium thiosulfate. Our findings illustrates that commercial Sudan III under reductive condition can forms a number of products, which some are known active genotoxins. The technique could be used to mimic important redox reactions in human metabolism or environment, highlighting the possible formation of by-products more toxic than the original dyes.en
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)-
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)-
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)-
dc.format.extent7784-7796-
dc.language.isoeng-
dc.publisherElectrochemical Science Group-
dc.sourceWeb of Science-
dc.subjectAromatic aminesen
dc.subjectsub productsen
dc.subjectelectrochemical reductionen
dc.subjectHPLCen
dc.subjectSudan dyesen
dc.titleElectrochemical Reduction as a Powerful Tool to Highlight the Possible Formation of By-Products More Toxic Than Sudan III Dyeen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniversidade de São Paulo (USP)-
dc.description.affiliationUniv Estadual Paulista UNESP, Dept Quim Analit, Inst Quim, BR-14800900 Araraquara, SP, Brazil-
dc.description.affiliationUniv São Paulo, Dept Anal Clin Toxicol & Bromatol, Fac Ciencias Farmaceut Ribeirao Preto, BR-14040903 Ribeirao Preto, SP, Brazil-
dc.description.affiliationUnespUniv Estadual Paulista UNESP, Dept Quim Analit, Inst Quim, BR-14800900 Araraquara, SP, Brazil-
dc.identifier.wosWOS:000309206900004-
dc.rights.accessRightsAcesso aberto-
dc.identifier.fileWOS000309206900004.pdf-
dc.relation.ispartofInternational Journal of Electrochemical Science-
dc.identifier.orcid0000-0002-2296-1393-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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