Journal
CHEMISTRY OF MATERIALS
Volume 20, Issue 21, Pages 6611-6616Publisher
AMER CHEMICAL SOC
DOI: 10.1021/cm800546h
Keywords
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Funding
- Chemical Sciences, Geosciences and Biosciences Division, Office of Basic Energy Sciences, Office of Science, U.S Department of Energy [DE-FG02-04ER15604]
- Brookhaven National Laboratory
- U.S. Department of Energy (DOE) [DE-FG02-04ER15604] Funding Source: U.S. Department of Energy (DOE)
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The hydrothermal Mo-V-based mixed oxide catalysts possessing the M1-phase structure were investigated by XANES and in situ X-ray diffraction under ambient and dynamic redox conditions in the presence of O-2 and H-2 at 693 K. Under ambient conditions, XANES, with the use of model compounds, suggested oxidation states of Nb, Te, Mo, and V close to 5+, 4+, 6+, and 4+, respectively, in the bulk M I phase. The oxidation state changes of Nb, Te, and Mo were not detected under the dynamic redox conditions employed, while the pre-edge peak of vanadium in the M I phase exhibited small, reproducible shifts, suggesting that VOx is the active catalytic species in the bulk M1-phase catalysts for selective (amin)oxidation of propane.
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