Dye Degradation Enhanced by Coupling Electrochemical Process and Heterogeneous Photocatalysis

Detalhes bibliográficos
Autor(a) principal: Santos,Lidiaine M.
Data de Publicação: 2015
Outros Autores: Amorim,Kamila P. de, Andrade,Leonardo S., Batista,Paulo S., Trovó,Alam G., Machado,Antonio E. H.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Journal of the Brazilian Chemical Society (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532015000901817
Resumo: In this study, we evaluated the combination between an electrochemical process, occurring in the dark, and a heterogeneous photocatalytic process for dye degradation, using the azo dye tartrazine as model of oxidizable substrate. TiO2 P25 and an Ag-doped TiO2 were used as photocatalysts in suspensions containing 50 mg L–1 of tartrazine. The best result, 74% of dye mineralization in 120 min of reaction, was obtained using TiO2 P25 as photocatalyst and a current density of 10 mA cm–2 in the electrochemical cell, a value 30% higher than the sum of the results obtained by heterogeneous photocatalysis (44%) and electrochemical oxidation (13%). The use of Ag-doped TiO2 did not result in significant improvement on tartrazine mineralization, due to the aggregation of these nanoparticles. Our results suggest that this process can be an alternative for a complete treatment (discoloration and mineralization) of tartrazine and most likely other azo dyes.
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spelling Dye Degradation Enhanced by Coupling Electrochemical Process and Heterogeneous Photocatalysisazo dyesadvanced oxidation processesdiscolorationmineralizationtitanium dioxideIn this study, we evaluated the combination between an electrochemical process, occurring in the dark, and a heterogeneous photocatalytic process for dye degradation, using the azo dye tartrazine as model of oxidizable substrate. TiO2 P25 and an Ag-doped TiO2 were used as photocatalysts in suspensions containing 50 mg L–1 of tartrazine. The best result, 74% of dye mineralization in 120 min of reaction, was obtained using TiO2 P25 as photocatalyst and a current density of 10 mA cm–2 in the electrochemical cell, a value 30% higher than the sum of the results obtained by heterogeneous photocatalysis (44%) and electrochemical oxidation (13%). The use of Ag-doped TiO2 did not result in significant improvement on tartrazine mineralization, due to the aggregation of these nanoparticles. Our results suggest that this process can be an alternative for a complete treatment (discoloration and mineralization) of tartrazine and most likely other azo dyes.Sociedade Brasileira de Química2015-09-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532015000901817Journal of the Brazilian Chemical Society v.26 n.9 2015reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.5935/0103-5053.20150158info:eu-repo/semantics/openAccessSantos,Lidiaine M.Amorim,Kamila P. deAndrade,Leonardo S.Batista,Paulo S.Trovó,Alam G.Machado,Antonio E. H.eng2015-09-11T00:00:00Zoai:scielo:S0103-50532015000901817Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2015-09-11T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Dye Degradation Enhanced by Coupling Electrochemical Process and Heterogeneous Photocatalysis
title Dye Degradation Enhanced by Coupling Electrochemical Process and Heterogeneous Photocatalysis
spellingShingle Dye Degradation Enhanced by Coupling Electrochemical Process and Heterogeneous Photocatalysis
Santos,Lidiaine M.
azo dyes
advanced oxidation processes
discoloration
mineralization
titanium dioxide
title_short Dye Degradation Enhanced by Coupling Electrochemical Process and Heterogeneous Photocatalysis
title_full Dye Degradation Enhanced by Coupling Electrochemical Process and Heterogeneous Photocatalysis
title_fullStr Dye Degradation Enhanced by Coupling Electrochemical Process and Heterogeneous Photocatalysis
title_full_unstemmed Dye Degradation Enhanced by Coupling Electrochemical Process and Heterogeneous Photocatalysis
title_sort Dye Degradation Enhanced by Coupling Electrochemical Process and Heterogeneous Photocatalysis
author Santos,Lidiaine M.
author_facet Santos,Lidiaine M.
Amorim,Kamila P. de
Andrade,Leonardo S.
Batista,Paulo S.
Trovó,Alam G.
Machado,Antonio E. H.
author_role author
author2 Amorim,Kamila P. de
Andrade,Leonardo S.
Batista,Paulo S.
Trovó,Alam G.
Machado,Antonio E. H.
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Santos,Lidiaine M.
Amorim,Kamila P. de
Andrade,Leonardo S.
Batista,Paulo S.
Trovó,Alam G.
Machado,Antonio E. H.
dc.subject.por.fl_str_mv azo dyes
advanced oxidation processes
discoloration
mineralization
titanium dioxide
topic azo dyes
advanced oxidation processes
discoloration
mineralization
titanium dioxide
description In this study, we evaluated the combination between an electrochemical process, occurring in the dark, and a heterogeneous photocatalytic process for dye degradation, using the azo dye tartrazine as model of oxidizable substrate. TiO2 P25 and an Ag-doped TiO2 were used as photocatalysts in suspensions containing 50 mg L–1 of tartrazine. The best result, 74% of dye mineralization in 120 min of reaction, was obtained using TiO2 P25 as photocatalyst and a current density of 10 mA cm–2 in the electrochemical cell, a value 30% higher than the sum of the results obtained by heterogeneous photocatalysis (44%) and electrochemical oxidation (13%). The use of Ag-doped TiO2 did not result in significant improvement on tartrazine mineralization, due to the aggregation of these nanoparticles. Our results suggest that this process can be an alternative for a complete treatment (discoloration and mineralization) of tartrazine and most likely other azo dyes.
publishDate 2015
dc.date.none.fl_str_mv 2015-09-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532015000901817
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532015000901817
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.5935/0103-5053.20150158
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Sociedade Brasileira de Química
publisher.none.fl_str_mv Sociedade Brasileira de Química
dc.source.none.fl_str_mv Journal of the Brazilian Chemical Society v.26 n.9 2015
reponame:Journal of the Brazilian Chemical Society (Online)
instname:Sociedade Brasileira de Química (SBQ)
instacron:SBQ
instname_str Sociedade Brasileira de Química (SBQ)
instacron_str SBQ
institution SBQ
reponame_str Journal of the Brazilian Chemical Society (Online)
collection Journal of the Brazilian Chemical Society (Online)
repository.name.fl_str_mv Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)
repository.mail.fl_str_mv ||office@jbcs.sbq.org.br
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