Characterization and reactivity of vanadia-molybdena catalysts supported on gamma-Al2O3

Citation
Kvr. Chary et al., Characterization and reactivity of vanadia-molybdena catalysts supported on gamma-Al2O3, APP CATAL A, 202(1), 2000, pp. 133-139
Citations number
52
Categorie Soggetti
Physical Chemistry/Chemical Physics","Chemical Engineering
Journal title
APPLIED CATALYSIS A-GENERAL
ISSN journal
0926860X → ACNP
Volume
202
Issue
1
Year of publication
2000
Pages
133 - 139
Database
ISI
SICI code
0926-860X(20000731)202:1<133:CAROVC>2.0.ZU;2-5
Abstract
The influence of molybdenum oxide on the dispersion of vanadium oxide suppo rted on alumina was investigated. A series of V2O5-MoO3 catalysts with vary ing MoO3 content ranging from 1-5% (w/w) were prepared by impregnation of p reviously prepared 10% V2O5/gamma-Al2O3 with requisite amounts of ammonium molybdate solution. Dispersion of vanadia was determined by oxygen chemisor ption at 195 K and was found to decrease with the increase of molybdena loa ding. The calcined catalyst samples were characterized by electron spin res onance (ESR) technique in their hydrogen reduced and unreduced conditions. The XRD results suggest formation of vanadium aluminate with the addition o f MoO3 to V2O5/gamma-Al2O3 catalyst. The ESR spectra of hydrogen reduced ca talysts show doublet structure at the low field parallel components, sugges ting the presence of two chemically distinct V4+ On alumina species. It was found that the nature of V4+ is strongly influenced by the added molybdena . The catalytic properties were evaluated for the vapour-phase oxidation of methanol. The activity during oxidation reaction was found to decrease wit h the increase of molybdena loading. However, the selectivity of formaldehy de was found to increase with molybdena loading, indicating that the added MoO3 created additional sites for partial oxidation reaction. The presence of molybdenum oxide inhibited the interaction between vanadium and alumina, leading to poor dispersion of vanadia and lower catalytic activity during selective oxidation. (C) 2000 Elsevier Science B.V. All rights reserved.