Please use this identifier to cite or link to this item: https://saber.ucv.ve/jspui/handle/10872/3220
Full metadata record
DC FieldValueLanguage
dc.contributor.authorGiuliante, Adriana-
dc.contributor.authorMarrero, Santiago-
dc.contributor.authorCarrillo, Valentina-
dc.contributor.authorFuentes, Keyla-
dc.contributor.authorAlbornoz, Alberto-
dc.contributor.authorBrito, Joaquin-
dc.contributor.authorBetancourt, Paulino-
dc.date.accessioned2013-04-21T02:51:19Z-
dc.date.available2013-04-21T02:51:19Z-
dc.date.issued2013-04-20-
dc.identifier.issn0798-4065-
dc.identifier.urihttp://hdl.handle.net/10872/3220-
dc.description.abstractA series of La/TiO2 solids were prepared using a conventional impregnation method. The samples were characterized by X-ray diffraction, nitrogen adsorption; point zero charge, FTIR monitoring adsorption of pyridine, and X-ray photoelectron spectroscopy (XPS). Characterization showed that the incorporation of 1%wt. of lanthanum in the oxidized phase partially promotes the anatase-rutile phase transformation under calcination at 500ºC. Also, the presence of this species lead the development of Brönsted surface acid sites and increase the zero point charge, which is desirable for the adsorption of certain species. Furthermore, the catalytic activity of the samples was tested in the photodegradation of 2-nitrophenol in aqueous solution, obtaining an increased activity for doped solids. The major intermediates identified by means of HPLC were cathecol and trihydroxibenzene. On the other hand, for the 1%La doped solid was also identified 2-aminophenol, standing a possible reductive way in the process.es_VE
dc.language.isoeses_VE
dc.subjectTiO2es_VE
dc.subjectfotocatalisises_VE
dc.subject2-nitrofenoles_VE
dc.subjectlantanoes_VE
dc.titlePROPIEDADES FISICOQUIMICAS DE SISTEMAS La/TiO2 EMPLEADOS EN LA FOTODEGRADACIÓN DE 2-NITROFENOL CON LUZ VISIBLE EN UN SIMULADOR SOLARes_VE
dc.typeWorking Paperes_VE
Appears in Collections:Artículos Publicados

Files in This Item:
File Description SizeFormat 
guiliante et al.pdf480.14 kBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.