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dc.contributor.authorZanoni, Maria Valnice Boldrin-
dc.contributor.authorSene, Jeosadaque J.-
dc.contributor.authorSelcuk, Huseyin-
dc.contributor.authorAnderson, Marc A.-
dc.date.accessioned2014-05-27T11:21:05Z-
dc.date.accessioned2016-10-25T18:19:36Z-
dc.date.available2014-05-27T11:21:05Z-
dc.date.available2016-10-25T18:19:36Z-
dc.date.issued2004-06-01-
dc.identifierhttp://dx.doi.org/10.1021/es0347080-
dc.identifier.citationEnvironmental Science and Technology, v. 38, n. 11, p. 3203-3208, 2004.-
dc.identifier.issn0013-936X-
dc.identifier.urihttp://hdl.handle.net/11449/67742-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/67742-
dc.description.abstractThe production of chlorine and hypochlorite is of great economical and technological interest due to their large-scale use in many kinds of commercial applications. Yet, the current processes are not without problems such as inevitable side reactions and the high cost of production. This work reports the photoelectrocatalytic oxidation of chloride ions to free chlorine as it has been investigated by using titanium dioxide (TiO2) and several metal-doped titanium dioxide (M-TiO2) material electrodes. An average concentration of 800 mg L-1 of free chlorine was obtained in an open-air reactor using a TiO2 thin-film electrode biased at +1.0 V (SCE) and illuminated by UV light. The M-doped electrodes have performed poorly compared with the pure TiO2 counterpart. Test solutions containing 0.05 mol L-1 NaCl pH 2.0-4.0 were found to be the best conditions for fast production of free chlorine. A complete investigation of all parameters that influence the global process of chlorine production by the photoelectrocatalytic method such as applied potential, concentration of NaCl, pH solution, and time is presented in detail. In addition, photocurrent vs potential curves and the reaction order are also discussed.en
dc.format.extent3203-3208-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectCatalysisen
dc.subjectCatalytic convertersen
dc.subjectCurve fittingen
dc.subjectElectrochemical electrodesen
dc.subjectpH effectsen
dc.subjectPhotochemical reactionsen
dc.subjectReaction kineticsen
dc.subjectActive chlorineen
dc.subjectPhotoelectrocatalytic productionen
dc.subjectThin film devicesen
dc.subjectchlorineen
dc.subjectsodium chlorideen
dc.subjecttitanium dioxideen
dc.subjectelectrochemistryen
dc.subjectcatalysisen
dc.subjectchemical reactionen
dc.subjectcrystallizationen
dc.subjectelectric currenten
dc.subjectelectrodeen
dc.subjectelectrolysisen
dc.subjectfilmen
dc.subjectilluminationen
dc.subjectoxidationen
dc.subjectparameteren
dc.subjectphotoreactivationen
dc.subjectreaction analysisen
dc.subjectultraviolet radiationen
dc.subjectChloridesen
dc.subjectChlorineen
dc.subjectConservation of Natural Resourcesen
dc.subjectCrystallizationen
dc.subjectElectrochemistryen
dc.subjectElectrodesen
dc.subjectHypochlorous Aciden
dc.subjectIonsen
dc.subjectNanotechnologyen
dc.subjectOxidation-Reductionen
dc.subjectPhotochemistryen
dc.titlePhotoelectrocatalytic production of active chlorine on nanocrystalline titanium dioxide thin-film electrodesen
dc.typeoutro-
dc.contributor.institutionUniversity of Wisconsin-Madison-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionFundacao Educacional de Barretos-
dc.description.affiliationEnviron. Chem. and Technol. Program University of Wisconsin-Madison, 660 North Park Street, Madison, WI 53706-
dc.description.affiliationInstituto de Quimica-UNESP, Caixa Postal 355, 14800-901, Araraquara-SP-
dc.description.affiliationFundacao Educacional de Barretos, Av. Prof. Roberto Frade Monte, 389, CEP 14783-226, Barretos-SP-
dc.description.affiliationUnespInstituto de Quimica-UNESP, Caixa Postal 355, 14800-901, Araraquara-SP-
dc.identifier.doi10.1021/es0347080-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofEnvironmental Science and Technology-
dc.identifier.scopus2-s2.0-2542451922-
dc.identifier.orcid0000-0002-2296-1393-
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