MODIFICATION OF THE SURFACE REACTIVITY OF VANADIUM ANTIMONATE CATALYSTS DURING CATALYTIC PROPANE AMMOXIDATION

Citation
G. Centi et S. Perathoner, MODIFICATION OF THE SURFACE REACTIVITY OF VANADIUM ANTIMONATE CATALYSTS DURING CATALYTIC PROPANE AMMOXIDATION, Applied catalysis. A, General, 124(2), 1995, pp. 317-337
Citations number
30
Categorie Soggetti
Chemistry Physical","Environmental Sciences
ISSN journal
0926860X
Volume
124
Issue
2
Year of publication
1995
Pages
317 - 337
Database
ISI
SICI code
0926-860X(1995)124:2<317:MOTSRO>2.0.ZU;2-Q
Abstract
The changes that take place in a vanadium antimonate catalyst during c atalytic propane ammoxidation were studied by transient reactivity exp eriments and infrared spectroscopy. The investigation was focused on b oth the change in catalytic behaviour of a fresh sample and the change in reactivity with stepwise increases in the concentration of one or more reagents while maintaining the concentration of the other reactan ts constant. The results obtained show that two main types of modifica tions are present: (1) A change in the reactivity from the fresh to th e activated samples due to the surface formation of a VSbO4 phase by r eaction of vanadium and antimony oxides that have not reacted during c alcination; this modification leads to formation of carbon oxides and a decrease in the rate of propane depletion as well as a considerable increase in the rate of acrylonitrile formation. (2) A change in the r eactivity of the activated sample which is a function of the redox cha racteristics of the reagent mixture; this modification does not change the rate of propane depletion, but rather only results in differences in the relative selectivity to products. The results also show that ( i) in the steady state, the activated catalyst is partially reduced in comparison with the same sample after treatment with oxygen and (ii) the rate of acrylonitrile formation is lower. Infrared results confirm the formation of oxygen vacancies in the catalyst upon interaction wi th ammonia and propene as well as the presence of these defects in the sample after the catalytic tests.