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Catalytic reactions on well-characterized vanadium oxide catalysts. 2. Oxidation of ethylene

Journal Article · · J. Phys. Chem.; (United States)
DOI:https://doi.org/10.1021/j150657a014· OSTI ID:6564153
Catalytic activities of unsupported and supported vanadium oxides for ethylene oxidation were investigated in relation to the catalyst structures. From results of reaction rates and steady-state catalyst structures at various O/sub 2/ concentrations, the active oxygen species was found to be the surface V=O species. The specific activity of the surface V=O species, or the turnover frequency, on unsupported V/sub 2/O/sub 5/ catalyst did not change with the treatment of the catalyst: neither fusion nor reduction-oxidation treatment affected the turnover frequency. This indicates that ethylene oxidation on vanadium oxide catalyst is a structure-insensitive reaction. The turnover frequency for V/sub 2/O/sub 5//TiO/sub 2/ (anatase) was considerably higher than that for V/sub 2/O/sub 5//TiO/sub 2/ (rutile) or unsupported V/sub 2/O/sub 5/ at any V/sub 2/O/sub 5/ content. This indicates the promoting effect of TiO/sub 2/ (anatase) support on the activity of vanadium oxide and provides experimental evidence for the validity of previous inference in solid-state chemistry. 14 references, 4 figures, 1 table.
Research Organization:
Nagoya Univ., Japan
OSTI ID:
6564153
Journal Information:
J. Phys. Chem.; (United States), Journal Name: J. Phys. Chem.; (United States) Vol. 88:13; ISSN JPCHA
Country of Publication:
United States
Language:
English