Identificador persistente para citar o vincular este elemento: http://hdl.handle.net/10553/43232
Campo DC Valoridioma
dc.contributor.authorSeck, Elhadji Idrissaen_US
dc.contributor.authorDoña Rodríguez, José Miguelen_US
dc.contributor.authorPulido Melián, Elisendaen_US
dc.contributor.authorFernández Rodríguez, Cristinaen_US
dc.contributor.authorGonzález Díaz, Oscar Manuelen_US
dc.contributor.authorPortillo-Carrizo, D.en_US
dc.contributor.authorPérez Peña, Jesúsen_US
dc.contributor.otherGonzalez Diaz, Oscar-
dc.contributor.otherPulido Melian, Elisenda-
dc.contributor.otherDona Rodriguez, Jose Miguel-
dc.contributor.otherFernandez-Rodriguez, Cristina-
dc.date.accessioned2018-11-21T13:36:09Z-
dc.date.available2018-11-21T13:36:09Z-
dc.date.issued2013en_US
dc.identifier.issn0021-9797en_US
dc.identifier.urihttp://hdl.handle.net/10553/43232-
dc.description.abstractTiO2 particles were prepared by sol–gel method alone and by sol–gel method combined with hydrothermal treatment. The structural and photocatalytic properties of the two series of photocatalysts were compared. XRD studies revealed that rutilization was faster in the series of photocatalysts, which had been additionally subjected to a hydrothermal process (SG-HT). The hydrothermally treated photocatalysts also displayed a higher specific surface area than those which had only been synthesized using the sol–gel process (SG) and subjected to low calcination temperatures of up to 873 K, while this tendency was inverted at higher temperatures. In accordance with the above observation, the hydrothermally treated series of photocatalysts had a lower particle size than the SG series calcined immediately after the sol–gel process up to 873 K, with this relation being inverted for the highest two temperatures which were studied (973 K and 1023 K) and which saw the commencement of rutilization. Increases in average particle size were observed for both series, with a polyhedral morphology seen as calcination temperature rose. FTIR studies highlighted the presence of the band at 2351 cm−1 in the SG-HT photocatalysts, characteristic of surface-adsorbed CO2. This was not seen in the SG or P25 photocatalysts. In terms of photoreactivity, the best photocatalyst in the SG-HT series was that calcined at 923 K and in the SG series at 1023 K (SG-1023). Comparing these two photocatalysts and the commercial P25 photocatalyst, SG-1023 was found to be the most photoactive in both the photodegradation and the mineralization of phenol.en_US
dc.languageengen_US
dc.publisher0021-9797
dc.relation"Producción de Fotocatalizadores Nanoestructurados Por Procesos de Bajo Coste y Alta Productividad Para Descontaminación de Aguas Residuales: Nanobacen_US
dc.relationNuevos Fotocatalizadores Basados en Tio2 Para Destoxificación de Efluentes Acuosos y Gaseosos: Sintesis, Modificación y Soporte.en_US
dc.relation.ispartofJournal of Colloid and Interface Scienceen_US
dc.sourceJournal of Colloid and Interface Science [ISSN 0021-9797], v. 400, p. 31-40en_US
dc.subject2301 química analíticaen_US
dc.subject.otherTiO2en_US
dc.subject.otherSol–gelen_US
dc.subject.otherHydrothermalen_US
dc.subject.otherPhotocatalysisen_US
dc.subject.otherPhenolen_US
dc.titleComparative study of nanocrystalline titanium dioxide obtained through sol-gel and sol-gel-hydrothermal synthesisen_US
dc.typeinfo:eu-repo/semantics/Articleen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.jcis.2013.03.019en_US
dc.identifier.scopus84876807519-
dc.identifier.isi000318464800005-
dcterms.isPartOfJournal Of Colloid And Interface Science
dcterms.sourceJournal Of Colloid And Interface Science[ISSN 0021-9797],v. 400, p. 31-40
dc.contributor.authorscopusid55327250800-
dc.contributor.authorscopusid6701567121-
dc.contributor.authorscopusid16743982000-
dc.contributor.authorscopusid8381553300-
dc.contributor.authorscopusid6602708293-
dc.contributor.authorscopusid36816370000-
dc.contributor.authorscopusid7004839316-
dc.description.lastpage40en_US
dc.description.firstpage31en_US
dc.relation.volume400en_US
dc.investigacionCienciasen_US
dc.type2Artículoen_US
dc.identifier.wosWOS:000318464800005-
dc.contributor.daisngid8375980-
dc.contributor.daisngid1159344-
dc.contributor.daisngid2293971-
dc.contributor.daisngid1959641-
dc.contributor.daisngid2523621-
dc.contributor.daisngid878298-
dc.contributor.daisngid5810923-
dc.contributor.daisngid1479300-
dc.identifier.investigatorRIDK-7365-2014-
dc.identifier.investigatorRIDL-2919-2014-
dc.identifier.investigatorRIDNo ID-
dc.identifier.investigatorRIDNo ID-
dc.utils.revisionen_US
dc.contributor.wosstandardWOS:Seck, EI-
dc.contributor.wosstandardWOS:Dona-Rodriguez, JM-
dc.contributor.wosstandardWOS:Melian, EP-
dc.contributor.wosstandardWOS:Fernandez-Rodriguez, C-
dc.contributor.wosstandardWOS:Gonzalez-Diaz, OM-
dc.contributor.wosstandardWOS:Portillo-Carrizo, D-
dc.contributor.wosstandardWOS:Perez-Pena, J-
dc.date.coverdateJunio 2013en_US
dc.identifier.ulpgcen_US
dc.contributor.buulpgcBU-BASen_US
dc.description.sjr1,19
dc.description.jcr3,552
dc.description.sjrqQ1
dc.description.jcrqQ2
dc.description.scieSCIE
item.grantfulltextnone-
item.fulltextSin texto completo-
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 Didácticas Específicas-
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.orcid0000-0003-3604-1544-
crisitem.author.orcid0000-0002-1999-9905-
crisitem.author.orcid0000-0001-6255-893X-
crisitem.author.orcid0000-0003-0876-8121-
crisitem.author.orcid0000-0003-1889-2281-
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.fullNameDoña Rodríguez, José Miguel-
crisitem.author.fullNamePulido Melián, Elisenda-
crisitem.author.fullNameFernández Rodríguez, Cristina-
crisitem.author.fullNameGonzález Díaz, Oscar Manuel-
crisitem.author.fullNamePérez Peña,Jesús-
crisitem.project.principalinvestigatorDoña Rodríguez, José Miguel-
crisitem.project.principalinvestigatorDoña Rodríguez, José Miguel-
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