Electrochemical reduction as a powerful tool to highlight the possible formation of by-products more toxic than sudan III dye

Detalhes bibliográficos
Autor(a) principal: Lizier, Thiago M. [UNESP]
Data de Publicação: 2012
Outros Autores: Zanoni, Thalita Boldrin, de Oliveira, Danielle Palma, Zanoni, Maria Valnice B. [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://hdl.handle.net/11449/227111
Resumo: The 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 tomimic important redox reactions in human metabolism or environment, highlighting the possible formation of by-products more toxic than the original dyes. © 2012 by ESG.
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spelling Electrochemical reduction as a powerful tool to highlight the possible formation of by-products more toxic than sudan III dyeAromatic aminesElectrochemical reductionHPLCSub productsSudan dyesThe 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 tomimic important redox reactions in human metabolism or environment, highlighting the possible formation of by-products more toxic than the original dyes. © 2012 by ESG.Instituto de Química Departamento de Química Analítica Universidade Estadual Paulista - UNESP, Rua Professor Francisco Degni, 55. Quitandinha, 14800-900, Araraquara/SPFaculdade de Ciências Farmacêuticas de Ribeirão Preto Departamento de Análises Clínicas Toxicológicas e Bromatológicas. Universidade de São Paulo, Avenida do Café, s/n, 14040-903, Ribeirão Preto/SPInstituto de Química Departamento de Química Analítica Universidade Estadual Paulista - UNESP, Rua Professor Francisco Degni, 55. Quitandinha, 14800-900, Araraquara/SPUniversidade Estadual Paulista (UNESP)Universidade de São Paulo (USP)Lizier, Thiago M. [UNESP]Zanoni, Thalita Boldrinde Oliveira, Danielle PalmaZanoni, Maria Valnice B. [UNESP]2022-04-29T06:48:18Z2022-04-29T06:48:18Z2012-12-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article7784-7796International Journal of Electrochemical Science, v. 7, n. 9, p. 7784-7796, 2012.1452-3981http://hdl.handle.net/11449/2271112-s2.0-84872855785Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengInternational Journal of Electrochemical Scienceinfo:eu-repo/semantics/openAccess2022-04-29T06:48:18Zoai:repositorio.unesp.br:11449/227111Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T19:14:57.856991Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Electrochemical reduction as a powerful tool to highlight the possible formation of by-products more toxic than sudan III dye
title Electrochemical reduction as a powerful tool to highlight the possible formation of by-products more toxic than sudan III dye
spellingShingle Electrochemical reduction as a powerful tool to highlight the possible formation of by-products more toxic than sudan III dye
Lizier, Thiago M. [UNESP]
Aromatic amines
Electrochemical reduction
HPLC
Sub products
Sudan dyes
title_short Electrochemical reduction as a powerful tool to highlight the possible formation of by-products more toxic than sudan III dye
title_full Electrochemical reduction as a powerful tool to highlight the possible formation of by-products more toxic than sudan III dye
title_fullStr Electrochemical reduction as a powerful tool to highlight the possible formation of by-products more toxic than sudan III dye
title_full_unstemmed Electrochemical reduction as a powerful tool to highlight the possible formation of by-products more toxic than sudan III dye
title_sort Electrochemical reduction as a powerful tool to highlight the possible formation of by-products more toxic than sudan III dye
author Lizier, Thiago M. [UNESP]
author_facet Lizier, Thiago M. [UNESP]
Zanoni, Thalita Boldrin
de Oliveira, Danielle Palma
Zanoni, Maria Valnice B. [UNESP]
author_role author
author2 Zanoni, Thalita Boldrin
de Oliveira, Danielle Palma
Zanoni, Maria Valnice B. [UNESP]
author2_role author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (UNESP)
Universidade de São Paulo (USP)
dc.contributor.author.fl_str_mv Lizier, Thiago M. [UNESP]
Zanoni, Thalita Boldrin
de Oliveira, Danielle Palma
Zanoni, Maria Valnice B. [UNESP]
dc.subject.por.fl_str_mv Aromatic amines
Electrochemical reduction
HPLC
Sub products
Sudan dyes
topic Aromatic amines
Electrochemical reduction
HPLC
Sub products
Sudan dyes
description The 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 tomimic important redox reactions in human metabolism or environment, highlighting the possible formation of by-products more toxic than the original dyes. © 2012 by ESG.
publishDate 2012
dc.date.none.fl_str_mv 2012-12-01
2022-04-29T06:48:18Z
2022-04-29T06:48:18Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv International Journal of Electrochemical Science, v. 7, n. 9, p. 7784-7796, 2012.
1452-3981
http://hdl.handle.net/11449/227111
2-s2.0-84872855785
identifier_str_mv International Journal of Electrochemical Science, v. 7, n. 9, p. 7784-7796, 2012.
1452-3981
2-s2.0-84872855785
url http://hdl.handle.net/11449/227111
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv International Journal of Electrochemical Science
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 7784-7796
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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