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Electrochemical decolorization of Rhodamine B dye: Influence of anode material, chloride concentration and current density

dc.contributor.authorBaddouh, Ali [UNESP]
dc.contributor.authorBessegato, Guilherme Garcia [UNESP]
dc.contributor.authorRguiti, Mohamed M.
dc.contributor.authorEl Ibrahimi, Brahim
dc.contributor.authorBazzi, Lahcen
dc.contributor.authorHilali, Mustapha
dc.contributor.authorZanoni, Maria Valnice Boldrin [UNESP]
dc.contributor.institutionIBN ZOHR University
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2018-12-11T17:36:16Z
dc.date.available2018-12-11T17:36:16Z
dc.date.issued2018-04-01
dc.description.abstractSurface water contamination by dyes released from a variety of industries is an environmental problem of great concern. However, electrochemical oxidation is a promising alternative for water treatment. In this paper, we studied the electrochemical oxidation of Rhodamine B (RhB) dye on the Ti/RuO2-IrO2 (DSA®) and SnO2 anodes comparing their efficiencies. The effect of some parameters, such as current density, initial pH (pH0), nature, concentration of electrolyte and temperature at the electrochemical oxidation was investigated evaluating the decolorization and the chemical oxygen demand (COD) removal at optimal conditions. Complete decolorization of RhB was achieved in the presence of chloride ions at different times using both electrodes. An optimum efficiency was obtained at pH 6.5, T°C. Also, the current density of 40cm-2 using the DSA electrode in NaCl 0.05L-1+ Na2SO4 0.1L-1 mixture solution as a supporting electrolyte, 100% color removal and 61.7% chemical oxygen demand removal after 90min of electrolysis were achieved. DSA showed better performance than SnO2 in wide operating conditions and was proved to be more cost-effective and more efficient. The effectiveness of the degradation is explained by indirect electrochemical oxidation, where in the presence of chlorides electrolyte leads to the electro-generation of strong oxidant species, such as Cl2 and ClO- ions, improving the efficiency of treatment at both electrodes.en
dc.description.affiliationApplied Chemistry-Physic Team Faculty of Sciences IBN ZOHR University, B.P. 8106 Cité Dakhla
dc.description.affiliationUniversidade Estadual Paulista (Unesp) Instituto de Química, Araraquara. Av. Prof. Francisco Degni 55
dc.description.affiliationUnespUniversidade Estadual Paulista (Unesp) Instituto de Química, Araraquara. Av. Prof. Francisco Degni 55
dc.format.extent2041-2047
dc.identifierhttp://dx.doi.org/10.1016/j.jece.2018.03.007
dc.identifier.citationJournal of Environmental Chemical Engineering, v. 6, n. 2, p. 2041-2047, 2018.
dc.identifier.doi10.1016/j.jece.2018.03.007
dc.identifier.file2-s2.0-85043582751.pdf
dc.identifier.issn2213-3437
dc.identifier.scopus2-s2.0-85043582751
dc.identifier.urihttp://hdl.handle.net/11449/179669
dc.language.isoeng
dc.relation.ispartofJournal of Environmental Chemical Engineering
dc.relation.ispartofsjr0,924
dc.rights.accessRightsAcesso aberto
dc.sourceScopus
dc.subjectDegradation
dc.subjectDSA
dc.subjectElectrochemical oxidation
dc.subjectRhodamine B
dc.subjectSnO2 electrode
dc.titleElectrochemical decolorization of Rhodamine B dye: Influence of anode material, chloride concentration and current densityen
dc.typeArtigo
dspace.entity.typePublication
unesp.author.orcid0000-0003-4500-1173[2]
unesp.author.orcid0000-0003-2838-5611[4]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Química, Araraquarapt
unesp.departmentQuímica Analítica - IQARpt

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