Characterization and reactivity of vanadium oxide supported on TiO 2 -SiO 2 mixed oxide support

Shee, Debaprasad and Mitra, Brishti and Chary, Komandur V R and Deo, Goutam (2018) Characterization and reactivity of vanadium oxide supported on TiO 2 -SiO 2 mixed oxide support. Molecular Catalysis. ISSN 2468-8231 (In Press)

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Abstract

A TiO2-SiO2 support, 90Ti-Si, containing 90 wt.% TiO2 was synthesized by the sol-gel method. Several supported vanadium oxide (vanadia) catalysts, xV90Ti-Si (x = 2–12.5 wt.%) were synthesized by incipient wetness impregnation method using this support. The catalysts and support were characterized and probed with the propane oxidative dehydrogenation (ODH) reaction. The support possesses no rutile phase and retains 30–40% of its initial surface area even after calcination at 1073 K. The surface area loss is accelerated in the presence of vanadia and the rutile phase appears below 1073 K. Surface vanadia species are present for the supported vanadia catalysts calcined at 673 K and the propane ODH activity and propene yield increases with vanadia loading. The ODH activity of the 2V90Ti-Si sample at 673 K is retained even after the catalyst is pre-calcined at 1023 K. Interestingly, the activity of the 4V90Ti-Si sample at 673 K reaches a maximum at an intermediate pre-calcination temperature. The higher vanadia loading samples deactivate with an increase in calcination temperature. The ODH reactivity reveals that the propene yield at iso-conversion increases with loading. Analysis of kinetic parameters also reveals that the rate constant ratio increases with vanadia loading

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IITH Creators:
IITH CreatorsORCiD
Shee, DebaprasadUNSPECIFIED
Item Type: Article
Uncontrolled Keywords: TiO2-SiO2 support, Vanadium oxide, DRIFT, Raman, Kinetic parameter
Subjects: Chemical Engineering
Divisions: Department of Chemical Engineering
Depositing User: Team Library
Date Deposited: 19 Feb 2018 04:50
Last Modified: 19 Feb 2018 04:50
URI: http://raiith.iith.ac.in/id/eprint/3791
Publisher URL: http://doi.org/10.1016/j.mcat.2018.01.020
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