You are in the accessibility menu

Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/67630
Full metadata record
DC FieldValueLanguage
dc.contributor.authorSelcuk, Huseyin-
dc.contributor.authorSene, Jeosadaque J.-
dc.contributor.authorZanoni, Maria Valnice Boldrin-
dc.contributor.authorSarikaya, Hasan Z.-
dc.contributor.authorAnderson, Marc A.-
dc.date.accessioned2014-05-27T11:21:01Z-
dc.date.accessioned2016-10-25T18:19:21Z-
dc.date.available2014-05-27T11:21:01Z-
dc.date.available2016-10-25T18:19:21Z-
dc.date.issued2004-02-01-
dc.identifierhttp://dx.doi.org/10.1016/j.chemosphere.2003.09.016-
dc.identifier.citationChemosphere, v. 54, n. 7, p. 969-974, 2004.-
dc.identifier.issn0045-6535-
dc.identifier.urihttp://hdl.handle.net/11449/67630-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/67630-
dc.description.abstractIn this study, the photoelectrocatalytic behavior of bromide and generation of bromine using TiO2 was investigated in the separate anode and cathode reaction chambers. Our results show that the generation of bromine begins around a flatband potential of -0.34 V vs. standard calomel electrode (SCE) at pH 3.0 under UV illumination and increases with an increase in positive potential, finally reaching a steady-state concentration at 1.0 V vs. SCE. Maximum bromine formation occurs over the range of pH 4-6, decreasing sharply at conditions where the pH > 7. © 2003 Elsevier Ltd. All rights reserved.en
dc.format.extent969-974-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectBromine generationen
dc.subjectElectrodesen
dc.subjectPhotoelectrocatalyticen
dc.subjectTitanium dioxideen
dc.subjectCatalyst activityen
dc.subjectNanostructured materialsen
dc.subjectpH effectsen
dc.subjectPhotoelectricityen
dc.subjectThin filmsen
dc.subjectStandard calomel electrodes (SCE)en
dc.subjectBromine compoundsen
dc.subjectbromideen
dc.subjectbromineen
dc.subjectmercurous chlorideen
dc.subjecttitanium dioxideen
dc.subjectphotochemistryen
dc.subjectchemical analysisen
dc.subjectchemical reactionen
dc.subjectconcentration (parameters)en
dc.subjectconcentration responseen
dc.subjectelectric potentialen
dc.subjectelectrodeen
dc.subjectfilmen
dc.subjectilluminationen
dc.subjectoxidationen
dc.subjectpHen
dc.subjectphotocatalysisen
dc.subjectporosityen
dc.subjectreaction analysisen
dc.subjectreactoren
dc.subjectsteady stateen
dc.subjectsynthesisen
dc.subjecttechniqueen
dc.subjectultraviolet radiationen
dc.subjectwater treatmenten
dc.subjectBromidesen
dc.subjectBromineen
dc.subjectCatalysisen
dc.subjectElectrochemistryen
dc.subjectHydrogen-Ion Concentrationen
dc.subjectKineticsen
dc.subjectTitaniumen
dc.titleBehavior of bromide in the photoelectrocatalytic process and bromine generation using nanoporous titanium dioxide thin-film electrodesen
dc.typeoutro-
dc.contributor.institutionUniversity of Wisconsin-Madison-
dc.contributor.institutionIstanbul Technical University-
dc.contributor.institutionFundacao Educacional de Barretos-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationEnviron. Chem. and Technol. Program University of Wisconsin-Madison, 660 N. Park Street, Madison, WI 53706 1484-
dc.description.affiliationDept. of Environmental Engineering Istanbul Technical University, 34 469 Maslak, Istanbul-
dc.description.affiliationFundacao Educacional de Barretos, Av. Prof. Roberto Frade Monte, 389, CEP 14783-226 Barretos-SP-
dc.description.affiliationInstituto de Quimica-UNESP, Caixa Postal 355, 14800-901 Araraquara-SP-
dc.description.affiliationUnespInstituto de Quimica-UNESP, Caixa Postal 355, 14800-901 Araraquara-SP-
dc.identifier.doi10.1016/j.chemosphere.2003.09.016-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofChemosphere-
dc.identifier.scopus2-s2.0-1642517073-
dc.identifier.orcid0000-0002-2296-1393-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

There are no files associated with this item.
Show simple item record Show full item record   View Statistics
 

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.