Electrochemical reduction as a powerful tool to highlight the possible formation of by-products more toxic than sudan III dye
Autor(a) principal: | |
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Data de Publicação: | 2012 |
Outros Autores: | , , |
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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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 |
|
_version_ |
1808129042096848896 |