Combination of photoelectrocatalysis and ozonation: A novel and powerful approach applied in Acid Yellow 1 mineralization

Detalhes bibliográficos
Autor(a) principal: Bessegato, Guilherme Garcia [UNESP]
Data de Publicação: 2016
Outros Autores: Cardoso, Juliano Carvalho [UNESP], da Silva, Bianca Ferreira [UNESP], Zanoni, Maria Valnice Boldrin [UNESP]
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.
id UNSP_22ebfb050f5f724b7feb76fb4b2f3eed
oai_identifier_str oai:repositorio.unesp.br:11449/171919
network_acronym_str UNSP
network_name_str Repositório Institucional da UNESP
repository_id_str 2946
spelling 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