Photoelectrochemical Hydrogen Generation and Concomitant Organic Dye Oxidation under TiO2 Nanotube
Autor(a) principal: | |
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Data de Publicação: | 2013 |
Outros Autores: | , , |
Tipo de documento: | Artigo de conferência |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1149/05036.0063ecst http://hdl.handle.net/11449/111443 |
Resumo: | The present work describes the photoelectrochemical hydrogen generation during a photodegradation of an organic compound. For this, it was chosen the reactive black 5 dye as a model of organic pollutant and its oxidation under TiO2 nanotube in a two compartment cell. The photoelectrocatalysis is conducted in 0.1 mol L-1 Na2SO4 pH 6 medium under photoanode biased at +1.0 V (SCE) and activated by UV and visible light using 150W Xe-Arc lamp (Oriel) and 125 W Hg lamp (Osram). The concomitant hydrogen production was monitored at cathodic compartment using a Pt cathode. Using optimized condition of Na2SO4 0.1 mol L-1 pH 6 as supporting electrolyte, applied potential of +1.0V it was verified 100% of discoloration and 72% of TOC removal of 1.0 x 10(-5) mol L-1 Reactive Black 5 dye after 120 min of treatment (rate constant of 10.6 x10(-2) min(-1)). The concomitant hydrogen generation was 44% in this condition. |
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Photoelectrochemical Hydrogen Generation and Concomitant Organic Dye Oxidation under TiO2 NanotubeThe present work describes the photoelectrochemical hydrogen generation during a photodegradation of an organic compound. For this, it was chosen the reactive black 5 dye as a model of organic pollutant and its oxidation under TiO2 nanotube in a two compartment cell. The photoelectrocatalysis is conducted in 0.1 mol L-1 Na2SO4 pH 6 medium under photoanode biased at +1.0 V (SCE) and activated by UV and visible light using 150W Xe-Arc lamp (Oriel) and 125 W Hg lamp (Osram). The concomitant hydrogen production was monitored at cathodic compartment using a Pt cathode. Using optimized condition of Na2SO4 0.1 mol L-1 pH 6 as supporting electrolyte, applied potential of +1.0V it was verified 100% of discoloration and 72% of TOC removal of 1.0 x 10(-5) mol L-1 Reactive Black 5 dye after 120 min of treatment (rate constant of 10.6 x10(-2) min(-1)). The concomitant hydrogen generation was 44% in this condition.Univ Estadual Paulista, Dept Analyt Chem, BR-14800900 Sao Paulo, BrazilUniv Estadual Paulista, Dept Analyt Chem, BR-14800900 Sao Paulo, BrazilElectrochemical Soc IncUniversidade Estadual Paulista (Unesp)Zanoni, M. V. B. [UNESP]Guaraldo, T. T. [UNESP]Brisard, G.Wieckowski, A.2014-12-03T13:08:39Z2014-12-03T13:08:39Z2013-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/conferenceObject63-70http://dx.doi.org/10.1149/05036.0063ecstElectrocatalysis 6. Pennington: Electrochemical Soc Inc, v. 50, n. 36, p. 63-70, 2013.1938-5862http://hdl.handle.net/11449/11144310.1149/05036.0063ecstWOS:000338309600007Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengElectrocatalysis 60,225info:eu-repo/semantics/openAccess2021-10-23T21:41:40Zoai:repositorio.unesp.br:11449/111443Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T23:52:23.814854Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Photoelectrochemical Hydrogen Generation and Concomitant Organic Dye Oxidation under TiO2 Nanotube |
title |
Photoelectrochemical Hydrogen Generation and Concomitant Organic Dye Oxidation under TiO2 Nanotube |
spellingShingle |
Photoelectrochemical Hydrogen Generation and Concomitant Organic Dye Oxidation under TiO2 Nanotube Zanoni, M. V. B. [UNESP] |
title_short |
Photoelectrochemical Hydrogen Generation and Concomitant Organic Dye Oxidation under TiO2 Nanotube |
title_full |
Photoelectrochemical Hydrogen Generation and Concomitant Organic Dye Oxidation under TiO2 Nanotube |
title_fullStr |
Photoelectrochemical Hydrogen Generation and Concomitant Organic Dye Oxidation under TiO2 Nanotube |
title_full_unstemmed |
Photoelectrochemical Hydrogen Generation and Concomitant Organic Dye Oxidation under TiO2 Nanotube |
title_sort |
Photoelectrochemical Hydrogen Generation and Concomitant Organic Dye Oxidation under TiO2 Nanotube |
author |
Zanoni, M. V. B. [UNESP] |
author_facet |
Zanoni, M. V. B. [UNESP] Guaraldo, T. T. [UNESP] Brisard, G. Wieckowski, A. |
author_role |
author |
author2 |
Guaraldo, T. T. [UNESP] Brisard, G. Wieckowski, A. |
author2_role |
author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (Unesp) |
dc.contributor.author.fl_str_mv |
Zanoni, M. V. B. [UNESP] Guaraldo, T. T. [UNESP] Brisard, G. Wieckowski, A. |
description |
The present work describes the photoelectrochemical hydrogen generation during a photodegradation of an organic compound. For this, it was chosen the reactive black 5 dye as a model of organic pollutant and its oxidation under TiO2 nanotube in a two compartment cell. The photoelectrocatalysis is conducted in 0.1 mol L-1 Na2SO4 pH 6 medium under photoanode biased at +1.0 V (SCE) and activated by UV and visible light using 150W Xe-Arc lamp (Oriel) and 125 W Hg lamp (Osram). The concomitant hydrogen production was monitored at cathodic compartment using a Pt cathode. Using optimized condition of Na2SO4 0.1 mol L-1 pH 6 as supporting electrolyte, applied potential of +1.0V it was verified 100% of discoloration and 72% of TOC removal of 1.0 x 10(-5) mol L-1 Reactive Black 5 dye after 120 min of treatment (rate constant of 10.6 x10(-2) min(-1)). The concomitant hydrogen generation was 44% in this condition. |
publishDate |
2013 |
dc.date.none.fl_str_mv |
2013-01-01 2014-12-03T13:08:39Z 2014-12-03T13:08:39Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/conferenceObject |
format |
conferenceObject |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1149/05036.0063ecst Electrocatalysis 6. Pennington: Electrochemical Soc Inc, v. 50, n. 36, p. 63-70, 2013. 1938-5862 http://hdl.handle.net/11449/111443 10.1149/05036.0063ecst WOS:000338309600007 |
url |
http://dx.doi.org/10.1149/05036.0063ecst http://hdl.handle.net/11449/111443 |
identifier_str_mv |
Electrocatalysis 6. Pennington: Electrochemical Soc Inc, v. 50, n. 36, p. 63-70, 2013. 1938-5862 10.1149/05036.0063ecst WOS:000338309600007 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Electrocatalysis 6 0,225 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
63-70 |
dc.publisher.none.fl_str_mv |
Electrochemical Soc Inc |
publisher.none.fl_str_mv |
Electrochemical Soc Inc |
dc.source.none.fl_str_mv |
Web of Science 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_ |
1808129560273747968 |