dc.contributorUniversidade Federal de São Carlos (UFSCar)
dc.contributorEmpresa Brasileira de Pesquisa Agropecuária (EMBRAPA)
dc.contributorUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-20T15:31:57Z
dc.date.accessioned2022-10-05T17:07:32Z
dc.date.available2014-05-20T15:31:57Z
dc.date.available2022-10-05T17:07:32Z
dc.date.created2014-05-20T15:31:57Z
dc.date.issued2009-01-01
dc.identifierJournal of Sol-gel Science and Technology. Dordrecht: Springer, v. 49, n. 1, p. 95-100, 2009.
dc.identifier0928-0707
dc.identifierhttp://hdl.handle.net/11449/40969
dc.identifier10.1007/s10971-008-1821-1
dc.identifierWOS:000261958100014
dc.identifier8498310891810082
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3911909
dc.description.abstractCommercial TiO2 nanoparticles were superficially modified through polymeric resins obtained from polymerization of citrate complexes of Y3+ and Al3+ with ethylenglycol. The materials were treated at 450 A degrees C for 4 h to obtain modified nanoparticles, which were characterized by HR-TEM, Zeta potential and surface area through N-2 fisisorption. Rhodamine B photodegradation by visible light irradiation and in presence of those modified nanoparticles was compared with the same process in presence of unmodified commercial TiO2 nanoparticles. It was observed, by UV-visible spectroscopy, that the catalytic photoactivity in presence of modified nanoparticles was smaller than that observed with commercial TiO2 nanoparticles. However, the surface modifier played an important role in the photodegradation kinetic process, showing a non-linear relation between modifier amount and photodegradation rate, presenting a maximum value at 0.8% (w/w).
dc.languageeng
dc.publisherSpringer
dc.relationJournal of Sol-Gel Science and Technology
dc.relation1.745
dc.relation0,477
dc.rightsAcesso restrito
dc.sourceWeb of Science
dc.subjectPhotodegradation
dc.subjectDye
dc.subjectTitanium dioxide
dc.subjectPhotocatalysis
dc.subjectWater treatment
dc.titleEffect of TiO2 surface modification in Rhodamine B photodegradation
dc.typeArtigo


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