Please use this identifier to cite or link to this item: http://hdl.handle.net/10553/45753
DC FieldValueLanguage
dc.contributor.authorSantiago, Dunia E.en_US
dc.contributor.authorPastrana-Martínez, Luisa M.en_US
dc.contributor.authorPulido-Melián, Elisendaen_US
dc.contributor.authorAraña Mesa, Francisco Javieren_US
dc.contributor.authorFaria, Joaquim L.en_US
dc.contributor.authorSilva, Adrián M.T.en_US
dc.contributor.authorGonzález-Díaz, Óscaren_US
dc.contributor.authorDoña-Rodríguez, José M.en_US
dc.date.accessioned2018-11-22T12:20:10Z-
dc.date.available2018-11-22T12:20:10Z-
dc.date.issued2018en_US
dc.identifier.issn0944-1344en_US
dc.identifier.urihttp://hdl.handle.net/10553/45753-
dc.description.abstractMagnetite (Fe3O4), a core-shell material (SiO2@Fe3O4), and reduced graphene oxide-Fe3O4 (referred as rGO-MN) were used as supports of a specific highly active TiO2 photocatalyst. Thermal treatments at 200 or 450 °C, different atmospheres (air or N2), and TiO2:support weight ratios (1.0, 1.5, or 2.0) were investigated. X-ray diffractograms revealed that magnetite is not oxidized to hematite when the core-shell SiO2@Fe3O4 material—or a N2 atmosphere (instead of air) in the thermal treatment—was employed to prepare the TiO2-based catalysts (the magnetic properties being preserved). The materials treated with N2 were first tested for degradation of imazalil (a well-known fungicide) in deionized water. The best compromise between the photocatalytic activity, magnetic separation, and Fe leached (1.61 mg L−1, i.e., below the threshold for water reuse in irrigation) was found for the magnetic catalyst prepared with SiO2@Fe3O4, an intermediate TiO2:support ratio (1.5), and treated at 200 °C under N2 atmosphere (i.e., SiO2@Fe3O4-EST-1.5-200-N2). This material was then tested for the treatment of imazalil in a synthetic wastewater, SW (with a chemical composition simulating an effluent resulting from fruit postharvest activity). This SW has a pH of 4.2 and the experiments were carried out at this natural pH0 and at neutral conditions (keeping pH at 7 along the reaction). The magnetic catalyst was more active than bare TiO2 for the treatment of imazalil in SW at natural pH. Since Fe leaching was observed (3.53 mg L−1), added H2O2 enhanced both imazalil degradation and mineralization. Conveniently, these catalysts can be readily recovered by using a conventional magnetic field, as demonstrated over three consecutive recycling runs.en_US
dc.languageengen_US
dc.publisher0944-1344-
dc.relationEliminacion Fotocatalitica de Mezclas de Nox y Covs en Emisiones Gaseosas Con Ti02 y Oxidos Mixtos.en_US
dc.relation.ispartofEnvironmental Science and Pollution Researchen_US
dc.sourceEnvironmental Science and Pollution Research[ISSN 0944-1344],v. 25, p. 27724-27736en_US
dc.subject3303 ingeniería y tecnología químicasen_US
dc.subject.otherImazalilen_US
dc.subject.otherPhotocatalysisen_US
dc.subject.otherTiO2en_US
dc.subject.otherMagneticen_US
dc.subject.otherFe3O4en_US
dc.subject.otherSiO2en_US
dc.titleTiO2-based (Fe3O4, SiO2, reduced graphene oxide) magnetically recoverable photocatalysts for imazalil degradation in a synthetic wastewateren_US
dc.typeinfo:eu-repo/semantics/articleen_US
dc.typeArticleen_US
dc.identifier.doi10.1007/s11356-018-1586-1en_US
dc.identifier.scopus85044199434-
dc.contributor.authorscopusid54985706700-
dc.contributor.authorscopusid23480128800-
dc.contributor.authorscopusid16743982000-
dc.contributor.authorscopusid7005207158-
dc.contributor.authorscopusid56871297100-
dc.contributor.authorscopusid56329177700-
dc.contributor.authorscopusid6602708293-
dc.contributor.authorscopusid6701567121-
dc.description.lastpage27736en_US
dc.description.firstpage27724en_US
dc.relation.volume25en_US
dc.investigacionIngeniería y Arquitecturaen_US
dc.type2Artículoen_US
dc.utils.revisionen_US
dc.identifier.ulpgcen_US
dc.contributor.buulpgcBU-BASen_US
dc.description.sjr0,828
dc.description.jcr2,914
dc.description.sjrqQ1
dc.description.jcrqQ2
dc.description.scieSCIE
item.grantfulltextnone-
item.fulltextSin texto completo-
crisitem.project.principalinvestigatorDoña Rodríguez, José Miguel-
crisitem.author.deptGIR IUNAT: Fotocatálisis y espectroscopía para aplicaciones medioambientales.-
crisitem.author.deptIU de Estudios Ambientales y Recursos Naturales-
crisitem.author.deptDepartamento de Ingeniería de Procesos-
crisitem.author.deptGIR IUNAT: Fotocatálisis y espectroscopía para aplicaciones medioambientales.-
crisitem.author.deptIU de Estudios Ambientales y Recursos Naturales-
crisitem.author.deptDepartamento de Química-
crisitem.author.deptGIR IUNAT: Fotocatálisis y espectroscopía para aplicaciones medioambientales.-
crisitem.author.deptIU de Estudios Ambientales y Recursos Naturales-
crisitem.author.deptDepartamento de Química-
crisitem.author.deptGIR IUNAT: Fotocatálisis y espectroscopía para aplicaciones medioambientales.-
crisitem.author.deptIU de Estudios Ambientales y Recursos Naturales-
crisitem.author.deptDepartamento de Química-
crisitem.author.deptGIR IUNAT: Fotocatálisis y espectroscopía para aplicaciones medioambientales.-
crisitem.author.deptIU de Estudios Ambientales y Recursos Naturales-
crisitem.author.deptDepartamento de Química-
crisitem.author.orcid0000-0003-2318-9152-
crisitem.author.orcid0000-0002-1999-9905-
crisitem.author.orcid0000-0002-5551-029X-
crisitem.author.orcid0000-0003-0876-8121-
crisitem.author.orcid0000-0003-3604-1544-
crisitem.author.parentorgIU de Estudios Ambientales y Recursos Naturales-
crisitem.author.parentorgIU de Estudios Ambientales y Recursos Naturales-
crisitem.author.parentorgIU de Estudios Ambientales y Recursos Naturales-
crisitem.author.parentorgIU de Estudios Ambientales y Recursos Naturales-
crisitem.author.parentorgIU de Estudios Ambientales y Recursos Naturales-
crisitem.author.fullNameSantiago Garcia, Dunia Esther-
crisitem.author.fullNamePulido Melián, Elisenda-
crisitem.author.fullNameAraña Mesa, Francisco Javier-
crisitem.author.fullNameGonzález Díaz, Oscar Manuel-
crisitem.author.fullNameDoña Rodríguez, José Miguel-
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