Dehydrogenation of i-butane on CrOx/SiO2 catalysts

Citation
A. Hakuli et al., Dehydrogenation of i-butane on CrOx/SiO2 catalysts, J CATALYSIS, 184(2), 1999, pp. 349-356
Citations number
48
Categorie Soggetti
Physical Chemistry/Chemical Physics","Chemical Engineering
Journal title
JOURNAL OF CATALYSIS
ISSN journal
00219517 → ACNP
Volume
184
Issue
2
Year of publication
1999
Pages
349 - 356
Database
ISI
SICI code
0021-9517(19990610)184:2<349:DOIOCC>2.0.ZU;2-C
Abstract
CrOx/SiO2 catalysts were characterized and their activity in the dehydrogen ation of i-butane was measured. Cr loading of the catalysts was between 1.1 and 11 wt% and preparation was by impregnation. The consumption of isolate d OH groups of SiO2 upon deposition of CrOx was followed by DRIFT-IR. The p resence of unreacted OH groups in the calcined catalyst at high loadings of Cr and the formation of alpha-Cr2O3 (XRD) showed, however, the tendency of CrOx to form clusters rather than a well-dispersed phase on SiO2. After ca lcination, 0.8-1.0 wt% Cr was stabilized in 6 + oxidation state (UV-VIS). O n the basis of H-2-TPR measurements it was suggested that these Cr6+ were s tabilized by anchoring on SiO2 or on the alpha-Cr2O3/SiO2 formed with incre asing Cr loading. The activities of the CrOx/SiO2 catalysts were studied in the dehydrogenation of i-butane at 540 degrees C by monitoring the product distributions with a rapid FT-IR gas analyzer. The dehydrogenation activit y is attributed to redox Cr in 3+ and 2+ oxidation states and tentatively t o part of the nonredox Cr3+ Th, relatively low selectivity of CrOx/SiO2 at low loadings of Cr was evidently due to the presence of Cr2+ directly ancho red to SiO2. (C) 1999 academic Press.