Dye Degradation Enhanced by Coupling Electrochemical Process and Heterogeneous Photocatalysis
Autor(a) principal: | |
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Data de Publicação: | 2015 |
Outros Autores: | , , , , |
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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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 |
_version_ |
1750318177474052096 |