On the performance of HOCl/Fe2+, HOCl/Fe2+/UVA, and HOCl/UVC processes using in situ electrogenerated active chlorine to mineralize the herbicide picloram

Detalhes bibliográficos
Autor(a) principal: Coledam, Douglas A. C.
Data de Publicação: 2018
Outros Autores: Sanchez-Montes, Isaac, Silva, Bianca F. [UNESP], Aquino, Jose M.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1016/j.apcatb.2017.12.072
http://hdl.handle.net/11449/164029
Resumo: Four different treatment methods based on the HO center dot production were assessed to oxidize and mineralize the herbicide picloram (PCL), which is considered very toxic and so is a potential contaminant of surface and ground water. The processes based on the Fenton type (homolysis reaction of HOCl by Fe+ ions) and photo-Fenton type reaction (using a 9 W UVA light) with in situ electrogenerated HOCl species, using a commercial D5Ae anode in the presence of Cl ions, led to poor mineralization performances in comparison to the HOCI/UVC process. In that case, the homolysis reaction of HOC1 mediated by a 5 or 9 W UVC light resulted in almost complete removal of the organic load within 12 h of treatment, from acidic to neutral solutions and using 1 g L-1 of NaCl concentration after optimization of the experimental conditions. When the HOCl/UVC process using a 5 W UVC light is compared to the electrochemical method using a boron-doped diamond anode (electrochemical/BDD), the oxidation and mineralization rates of the HOC1/UVC process were always superior, with- 95% removal of total organic carbon (TOC) after 12 h treatment. The energy consumption per unit mass of removed TOC remained around 4 and 8 kW h g(-1) for the HOC1/UVC and electrochemical/BDD treatment processes after 90% removal of TOC, respectively, even considering the energy consumption of the UVC lamp. In the final treatment stages, high CO2 conversions were obtained using both methods, as the generated intermediates were almost completely eliminated. Finally, the HOCI/UVC process is a reasonable option to treat solutions contaminated with organic pollutants as the common problems associated with the Fenton based (acidic solution, Fe2+ ion recovery, generation of H2O2) and electrochemical/BDD (mass transport) processes can be readily circumvented.
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spelling On the performance of HOCl/Fe2+, HOCl/Fe2+/UVA, and HOCl/UVC processes using in situ electrogenerated active chlorine to mineralize the herbicide picloramFenton like reactionSynthetic organic pollutantsOrganochlorine compoundsMixed oxide anodeHybrid methodsFour different treatment methods based on the HO center dot production were assessed to oxidize and mineralize the herbicide picloram (PCL), which is considered very toxic and so is a potential contaminant of surface and ground water. The processes based on the Fenton type (homolysis reaction of HOCl by Fe+ ions) and photo-Fenton type reaction (using a 9 W UVA light) with in situ electrogenerated HOCl species, using a commercial D5Ae anode in the presence of Cl ions, led to poor mineralization performances in comparison to the HOCI/UVC process. In that case, the homolysis reaction of HOC1 mediated by a 5 or 9 W UVC light resulted in almost complete removal of the organic load within 12 h of treatment, from acidic to neutral solutions and using 1 g L-1 of NaCl concentration after optimization of the experimental conditions. When the HOCl/UVC process using a 5 W UVC light is compared to the electrochemical method using a boron-doped diamond anode (electrochemical/BDD), the oxidation and mineralization rates of the HOC1/UVC process were always superior, with- 95% removal of total organic carbon (TOC) after 12 h treatment. The energy consumption per unit mass of removed TOC remained around 4 and 8 kW h g(-1) for the HOC1/UVC and electrochemical/BDD treatment processes after 90% removal of TOC, respectively, even considering the energy consumption of the UVC lamp. In the final treatment stages, high CO2 conversions were obtained using both methods, as the generated intermediates were almost completely eliminated. Finally, the HOCI/UVC process is a reasonable option to treat solutions contaminated with organic pollutants as the common problems associated with the Fenton based (acidic solution, Fe2+ ion recovery, generation of H2O2) and electrochemical/BDD (mass transport) processes can be readily circumvented.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Univ Fed Sao Carlos, Dept Quim, BR-13565905 Sao Carlos, SP, BrazilUniv Estadual Paulista, Inst Quim Araraquara, Dept Quim Analit, BR-14800900 Araraquara, SP, BrazilUniv Estadual Paulista, Inst Quim Araraquara, Dept Quim Analit, BR-14800900 Araraquara, SP, BrazilFAPESP: 2008/10449-7Elsevier B.V.Universidade Federal de São Carlos (UFSCar)Universidade Estadual Paulista (Unesp)Coledam, Douglas A. C.Sanchez-Montes, IsaacSilva, Bianca F. [UNESP]Aquino, Jose M.2018-11-26T17:48:50Z2018-11-26T17:48:50Z2018-07-05info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article170-177application/pdfhttp://dx.doi.org/10.1016/j.apcatb.2017.12.072Applied Catalysis B-environmental. Amsterdam: Elsevier Science Bv, v. 227, p. 170-177, 2018.0926-3373http://hdl.handle.net/11449/16402910.1016/j.apcatb.2017.12.072WOS:000428491000018WOS000428491000018.pdfWeb of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengApplied Catalysis B-environmental3,152info:eu-repo/semantics/openAccess2023-10-04T06:05:26Zoai:repositorio.unesp.br:11449/164029Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462023-10-04T06:05:26Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv On the performance of HOCl/Fe2+, HOCl/Fe2+/UVA, and HOCl/UVC processes using in situ electrogenerated active chlorine to mineralize the herbicide picloram
title On the performance of HOCl/Fe2+, HOCl/Fe2+/UVA, and HOCl/UVC processes using in situ electrogenerated active chlorine to mineralize the herbicide picloram
spellingShingle On the performance of HOCl/Fe2+, HOCl/Fe2+/UVA, and HOCl/UVC processes using in situ electrogenerated active chlorine to mineralize the herbicide picloram
Coledam, Douglas A. C.
Fenton like reaction
Synthetic organic pollutants
Organochlorine compounds
Mixed oxide anode
Hybrid methods
title_short On the performance of HOCl/Fe2+, HOCl/Fe2+/UVA, and HOCl/UVC processes using in situ electrogenerated active chlorine to mineralize the herbicide picloram
title_full On the performance of HOCl/Fe2+, HOCl/Fe2+/UVA, and HOCl/UVC processes using in situ electrogenerated active chlorine to mineralize the herbicide picloram
title_fullStr On the performance of HOCl/Fe2+, HOCl/Fe2+/UVA, and HOCl/UVC processes using in situ electrogenerated active chlorine to mineralize the herbicide picloram
title_full_unstemmed On the performance of HOCl/Fe2+, HOCl/Fe2+/UVA, and HOCl/UVC processes using in situ electrogenerated active chlorine to mineralize the herbicide picloram
title_sort On the performance of HOCl/Fe2+, HOCl/Fe2+/UVA, and HOCl/UVC processes using in situ electrogenerated active chlorine to mineralize the herbicide picloram
author Coledam, Douglas A. C.
author_facet Coledam, Douglas A. C.
Sanchez-Montes, Isaac
Silva, Bianca F. [UNESP]
Aquino, Jose M.
author_role author
author2 Sanchez-Montes, Isaac
Silva, Bianca F. [UNESP]
Aquino, Jose M.
author2_role author
author
author
dc.contributor.none.fl_str_mv Universidade Federal de São Carlos (UFSCar)
Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Coledam, Douglas A. C.
Sanchez-Montes, Isaac
Silva, Bianca F. [UNESP]
Aquino, Jose M.
dc.subject.por.fl_str_mv Fenton like reaction
Synthetic organic pollutants
Organochlorine compounds
Mixed oxide anode
Hybrid methods
topic Fenton like reaction
Synthetic organic pollutants
Organochlorine compounds
Mixed oxide anode
Hybrid methods
description Four different treatment methods based on the HO center dot production were assessed to oxidize and mineralize the herbicide picloram (PCL), which is considered very toxic and so is a potential contaminant of surface and ground water. The processes based on the Fenton type (homolysis reaction of HOCl by Fe+ ions) and photo-Fenton type reaction (using a 9 W UVA light) with in situ electrogenerated HOCl species, using a commercial D5Ae anode in the presence of Cl ions, led to poor mineralization performances in comparison to the HOCI/UVC process. In that case, the homolysis reaction of HOC1 mediated by a 5 or 9 W UVC light resulted in almost complete removal of the organic load within 12 h of treatment, from acidic to neutral solutions and using 1 g L-1 of NaCl concentration after optimization of the experimental conditions. When the HOCl/UVC process using a 5 W UVC light is compared to the electrochemical method using a boron-doped diamond anode (electrochemical/BDD), the oxidation and mineralization rates of the HOC1/UVC process were always superior, with- 95% removal of total organic carbon (TOC) after 12 h treatment. The energy consumption per unit mass of removed TOC remained around 4 and 8 kW h g(-1) for the HOC1/UVC and electrochemical/BDD treatment processes after 90% removal of TOC, respectively, even considering the energy consumption of the UVC lamp. In the final treatment stages, high CO2 conversions were obtained using both methods, as the generated intermediates were almost completely eliminated. Finally, the HOCI/UVC process is a reasonable option to treat solutions contaminated with organic pollutants as the common problems associated with the Fenton based (acidic solution, Fe2+ ion recovery, generation of H2O2) and electrochemical/BDD (mass transport) processes can be readily circumvented.
publishDate 2018
dc.date.none.fl_str_mv 2018-11-26T17:48:50Z
2018-11-26T17:48:50Z
2018-07-05
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.2017.12.072
Applied Catalysis B-environmental. Amsterdam: Elsevier Science Bv, v. 227, p. 170-177, 2018.
0926-3373
http://hdl.handle.net/11449/164029
10.1016/j.apcatb.2017.12.072
WOS:000428491000018
WOS000428491000018.pdf
url http://dx.doi.org/10.1016/j.apcatb.2017.12.072
http://hdl.handle.net/11449/164029
identifier_str_mv Applied Catalysis B-environmental. Amsterdam: Elsevier Science Bv, v. 227, p. 170-177, 2018.
0926-3373
10.1016/j.apcatb.2017.12.072
WOS:000428491000018
WOS000428491000018.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 170-177
application/pdf
dc.publisher.none.fl_str_mv Elsevier B.V.
publisher.none.fl_str_mv Elsevier B.V.
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
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