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

dc.contributor.authorBessegato, Guilherme Garcia [UNESP]
dc.contributor.authorCardoso, Juliano Carvalho [UNESP]
dc.contributor.authorda Silva, Bianca Ferreira [UNESP]
dc.contributor.authorZanoni, Maria Valnice Boldrin [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2018-12-11T16:57:44Z
dc.date.available2018-12-11T16:57:44Z
dc.date.issued2016-01-01
dc.description.abstractPhotoelectrocatalytic 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.en
dc.description.affiliationDepartment of Analytical Chemistry, Institute of Chemistry, Universidade Estadual Paulista Júlio de Mesquita Filho-UNESP, Av. Prof. Francisco Degni, 55
dc.description.affiliationUnespDepartment of Analytical Chemistry, Institute of Chemistry, Universidade Estadual Paulista Júlio de Mesquita Filho-UNESP, Av. Prof. Francisco Degni, 55
dc.format.extent161-168
dc.identifierhttp://dx.doi.org/10.1016/j.apcatb.2015.06.013
dc.identifier.citationApplied Catalysis B: Environmental, v. 180, p. 161-168.
dc.identifier.doi10.1016/j.apcatb.2015.06.013
dc.identifier.file2-s2.0-84936791472.pdf
dc.identifier.issn0926-3373
dc.identifier.scopus2-s2.0-84936791472
dc.identifier.urihttp://hdl.handle.net/11449/171919
dc.language.isoeng
dc.relation.ispartofApplied Catalysis B: Environmental
dc.relation.ispartofsjr3,152
dc.rights.accessRightsAcesso aberto
dc.sourceScopus
dc.subjectCatalytic ozonation
dc.subjectDye degradation
dc.subjectOzone assisted Photoelectrocatalysis
dc.subjectPhotoelectrocatalytic oxidation
dc.titleCombination of photoelectrocatalysis and ozonation: A novel and powerful approach applied in Acid Yellow 1 mineralizationen
dc.typeArtigo

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