Please use this identifier to cite or link to this item: doi:10.22028/D291-24270
Title: V2O5/TiO2 catalyst xerogels : method of preparation and characterization
Author(s): Rodella, Cristiane B.
Franco, Roberto W. A.
Magon, Claudio J.
Donoso, Jose P.
Nunes, Luis A. O.
Saeki, Margarida J.
Aegerter, Michel A.
Florentino, Ariovaldo O.
Language: English
Year of Publication: 2002
OPUS Source: Journal of sol-gel science and technology. - 25. 2002, S. 75-82
SWD key words: Sol-Gel-Verfahren
Vanadium
Vanadiumdioxid
Titan
Katalyse
Ethanol
Katalytische Oxidation
Röntgendiffraktometrie
DDC notations: 620 Engineering and machine engineering
Publikation type: Journal Article
Abstract: This work describes a modified sol-gel method for the preparation of V2O5/TiO2 catalysts. The samples have been characterized by N2 adsorption at 77 K, X-ray diffractometry (XRD), Scanning Electronic Microscopy (SEM/EDX) and Fourier Transform Infrared Spectroscopy (FT-IR). The surface area increases with the vanadia loading from 24 m2 g-1 for pure TiO2 to 87 m2 g-1 for 9wt% of V2O5. The rutile form is predominant for pure TiO2 but becomes enriched with anatase phase when vanadia loading is increased. No crystalline V2O5 phase was observed in the diffractograms of the catalysts. Analysis by SEM showed heterogeneous granulation of particles with high vanadium dispersion. Two species of surface vanadium were observed by FT-IR spectroscopy: a monomeric vanadyl and polymeric vanadates. The vanadyl/vanadate ration remains practically constant. Ethanol oxidation was used as a catalytic test in a temperature range from 350 to 560 K. The catalytic activity starts around 380K. For the sample with 9 wt% of vanadia, the conversion of ethanol into acetaldehyde as the main product was approximately 90% at 473 K.
Link to this record: urn:nbn:de:bsz:291-scidok-25168
hdl:20.500.11880/24326
http://dx.doi.org/10.22028/D291-24270
Date of registration: 15-Dec-2009
Faculty: SE - Sonstige Einrichtungen
Department: SE - INM Leibniz-Institut für Neue Materialien
Collections:INM
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