PROPANE OXYDEHYDROGENATION REACTION ON A VPO TIO2 CATALYST - ROLE OF THE NATURE OF ACID SITES DETERMINED BY DYNAMIC IN-SITU IR STUDIES/

Citation
L. Savary et al., PROPANE OXYDEHYDROGENATION REACTION ON A VPO TIO2 CATALYST - ROLE OF THE NATURE OF ACID SITES DETERMINED BY DYNAMIC IN-SITU IR STUDIES/, Catalysis today, 32(1-4), 1996, pp. 57-61
Citations number
17
Categorie Soggetti
Engineering, Chemical","Chemistry Applied","Chemistry Physical
Journal title
ISSN journal
09205861
Volume
32
Issue
1-4
Year of publication
1996
Pages
57 - 61
Database
ISI
SICI code
0920-5861(1996)32:1-4<57:POROAV>2.0.ZU;2-S
Abstract
A VPO/TiO2 catalyst tested in the oxydehydrogenation reaction (ODH) of propane between 300 and 400 degrees C shows satisfactory performances (up to 80% of propene selectivity at 2% of propane conversion at 300 degrees C or 56% of propene selectivity at 9% of propane conversion at 400 degrees C). Addition of water or pyridine in the feed gas tends t o decrease the propane conversion and enhances the propene selectivity . It is shown that water increases the number of Bronsted surface acid sites by dissociative adsorption which, in turn, enhances propene sel ectivity at the expense of the COx selectivity. These results are in g ood agreement with spectroscopic IR observations performed under catal ytic conditions showing that the Lewis acid sites are linked to COx fo rmation, whereas it seems that Bronsted sites would rather be linked t o propene formation.