Combination of photoelectrocatalysis and ozonation: A novel and powerful approach applied in Acid Yellow 1 mineralization
Autor(a) principal: | |
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Data de Publicação: | 2016 |
Outros Autores: | , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1016/j.apcatb.2015.06.013 http://hdl.handle.net/11449/171919 |
Resumo: | Photoelectrocatalytic oxidation (PEC) is known to be a powerful technique employed with the aim of promoting organic degradation. Its efficiency is nonetheless found to be dramatically decreased when applied in highly concentrated effluent treatment owing to the reduced transparency which minimizes the photons reaching the semiconductor surface. In light of that, the present work seeks to describe a novel combination of photoelectrocatalysis and ozonation (O<inf>3</inf>+PEC) techniques, aiming at achieving a faster decolorization of a highly concentrated solution and a higher rate of mineralization. The Acid Yellow 1 dye (AY1), widely used in cosmetics was chosen as a colorful solution model. TiO<inf>2</inf> nanotubes electrode was used as photoanode in an annular bubble reactor operating at 2.0V with UV-B irradiation in the presence of 1.25×10<sup>-4</sup>molmin<sup>-1</sup> of O<inf>3</inf>. The main factors interfering in the O<inf>3</inf>+PEC process were optimized through UV/vis spectrophotometry, total organic carbon (TOC) and mass spectrometry measurements. After 20min of treatment using the combined system, 100% of decolorization was observed while a total mineralization was seen following 60min of treatment even in effluents containing 100ppm AY1. Concomitantly, the combined system (O<inf>3</inf>+PEC) showed higher decolorization rate constant and lower energy consumption compared to the other techniques, showing that O<inf>3</inf>+ PEC is a successful, efficient and cost-effective alternative for water treatment. |
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Combination of photoelectrocatalysis and ozonation: A novel and powerful approach applied in Acid Yellow 1 mineralizationCatalytic ozonationDye degradationOzone assisted PhotoelectrocatalysisPhotoelectrocatalytic oxidationPhotoelectrocatalytic oxidation (PEC) is known to be a powerful technique employed with the aim of promoting organic degradation. Its efficiency is nonetheless found to be dramatically decreased when applied in highly concentrated effluent treatment owing to the reduced transparency which minimizes the photons reaching the semiconductor surface. In light of that, the present work seeks to describe a novel combination of photoelectrocatalysis and ozonation (O<inf>3</inf>+PEC) techniques, aiming at achieving a faster decolorization of a highly concentrated solution and a higher rate of mineralization. The Acid Yellow 1 dye (AY1), widely used in cosmetics was chosen as a colorful solution model. TiO<inf>2</inf> nanotubes electrode was used as photoanode in an annular bubble reactor operating at 2.0V with UV-B irradiation in the presence of 1.25×10<sup>-4</sup>molmin<sup>-1</sup> of O<inf>3</inf>. The main factors interfering in the O<inf>3</inf>+PEC process were optimized through UV/vis spectrophotometry, total organic carbon (TOC) and mass spectrometry measurements. After 20min of treatment using the combined system, 100% of decolorization was observed while a total mineralization was seen following 60min of treatment even in effluents containing 100ppm AY1. Concomitantly, the combined system (O<inf>3</inf>+PEC) showed higher decolorization rate constant and lower energy consumption compared to the other techniques, showing that O<inf>3</inf>+ PEC is a successful, efficient and cost-effective alternative for water treatment.Department of Analytical Chemistry, Institute of Chemistry, Universidade Estadual Paulista Júlio de Mesquita Filho-UNESP, Av. Prof. Francisco Degni, 55Department of Analytical Chemistry, Institute of Chemistry, Universidade Estadual Paulista Júlio de Mesquita Filho-UNESP, Av. Prof. Francisco Degni, 55Universidade Estadual Paulista (Unesp)Bessegato, Guilherme Garcia [UNESP]Cardoso, Juliano Carvalho [UNESP]da Silva, Bianca Ferreira [UNESP]Zanoni, Maria Valnice Boldrin [UNESP]2018-12-11T16:57:44Z2018-12-11T16:57:44Z2016-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article161-168application/pdfhttp://dx.doi.org/10.1016/j.apcatb.2015.06.013Applied Catalysis B: Environmental, v. 180, p. 161-168.0926-3373http://hdl.handle.net/11449/17191910.1016/j.apcatb.2015.06.0132-s2.0-849367914722-s2.0-84936791472.pdfScopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengApplied Catalysis B: Environmental3,152info:eu-repo/semantics/openAccess2023-11-05T06:06:57Zoai:repositorio.unesp.br:11449/171919Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T16:56:34.423106Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Combination of photoelectrocatalysis and ozonation: A novel and powerful approach applied in Acid Yellow 1 mineralization |
title |
Combination of photoelectrocatalysis and ozonation: A novel and powerful approach applied in Acid Yellow 1 mineralization |
spellingShingle |
Combination of photoelectrocatalysis and ozonation: A novel and powerful approach applied in Acid Yellow 1 mineralization Bessegato, Guilherme Garcia [UNESP] Catalytic ozonation Dye degradation Ozone assisted Photoelectrocatalysis Photoelectrocatalytic oxidation |
title_short |
Combination of photoelectrocatalysis and ozonation: A novel and powerful approach applied in Acid Yellow 1 mineralization |
title_full |
Combination of photoelectrocatalysis and ozonation: A novel and powerful approach applied in Acid Yellow 1 mineralization |
title_fullStr |
Combination of photoelectrocatalysis and ozonation: A novel and powerful approach applied in Acid Yellow 1 mineralization |
title_full_unstemmed |
Combination of photoelectrocatalysis and ozonation: A novel and powerful approach applied in Acid Yellow 1 mineralization |
title_sort |
Combination of photoelectrocatalysis and ozonation: A novel and powerful approach applied in Acid Yellow 1 mineralization |
author |
Bessegato, Guilherme Garcia [UNESP] |
author_facet |
Bessegato, Guilherme Garcia [UNESP] Cardoso, Juliano Carvalho [UNESP] da Silva, Bianca Ferreira [UNESP] Zanoni, Maria Valnice Boldrin [UNESP] |
author_role |
author |
author2 |
Cardoso, Juliano Carvalho [UNESP] da Silva, Bianca Ferreira [UNESP] Zanoni, Maria Valnice Boldrin [UNESP] |
author2_role |
author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (Unesp) |
dc.contributor.author.fl_str_mv |
Bessegato, Guilherme Garcia [UNESP] Cardoso, Juliano Carvalho [UNESP] da Silva, Bianca Ferreira [UNESP] Zanoni, Maria Valnice Boldrin [UNESP] |
dc.subject.por.fl_str_mv |
Catalytic ozonation Dye degradation Ozone assisted Photoelectrocatalysis Photoelectrocatalytic oxidation |
topic |
Catalytic ozonation Dye degradation Ozone assisted Photoelectrocatalysis Photoelectrocatalytic oxidation |
description |
Photoelectrocatalytic oxidation (PEC) is known to be a powerful technique employed with the aim of promoting organic degradation. Its efficiency is nonetheless found to be dramatically decreased when applied in highly concentrated effluent treatment owing to the reduced transparency which minimizes the photons reaching the semiconductor surface. In light of that, the present work seeks to describe a novel combination of photoelectrocatalysis and ozonation (O<inf>3</inf>+PEC) techniques, aiming at achieving a faster decolorization of a highly concentrated solution and a higher rate of mineralization. The Acid Yellow 1 dye (AY1), widely used in cosmetics was chosen as a colorful solution model. TiO<inf>2</inf> nanotubes electrode was used as photoanode in an annular bubble reactor operating at 2.0V with UV-B irradiation in the presence of 1.25×10<sup>-4</sup>molmin<sup>-1</sup> of O<inf>3</inf>. The main factors interfering in the O<inf>3</inf>+PEC process were optimized through UV/vis spectrophotometry, total organic carbon (TOC) and mass spectrometry measurements. After 20min of treatment using the combined system, 100% of decolorization was observed while a total mineralization was seen following 60min of treatment even in effluents containing 100ppm AY1. Concomitantly, the combined system (O<inf>3</inf>+PEC) showed higher decolorization rate constant and lower energy consumption compared to the other techniques, showing that O<inf>3</inf>+ PEC is a successful, efficient and cost-effective alternative for water treatment. |
publishDate |
2016 |
dc.date.none.fl_str_mv |
2016-01-01 2018-12-11T16:57:44Z 2018-12-11T16:57:44Z |
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 |
http://dx.doi.org/10.1016/j.apcatb.2015.06.013 Applied Catalysis B: Environmental, v. 180, p. 161-168. 0926-3373 http://hdl.handle.net/11449/171919 10.1016/j.apcatb.2015.06.013 2-s2.0-84936791472 2-s2.0-84936791472.pdf |
url |
http://dx.doi.org/10.1016/j.apcatb.2015.06.013 http://hdl.handle.net/11449/171919 |
identifier_str_mv |
Applied Catalysis B: Environmental, v. 180, p. 161-168. 0926-3373 10.1016/j.apcatb.2015.06.013 2-s2.0-84936791472 2-s2.0-84936791472.pdf |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Applied Catalysis B: Environmental 3,152 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
161-168 application/pdf |
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_ |
1808128724921483264 |