Abstract
Fifteen distinct MgO-V2O5, MgO-MoO3, MgO-V2O5-MoO3, and V2O 5-MoO3 compositions were prepared using sol-gel chemistry and their selectivities and conversions for propane oxidative dehydrogenation (ODH) to propylene were measured. The vanadates were more active than the molybdates at lower temperatures; however, the molybdates exhibited higher selectivities at similar conversions. An increase in both ODH conversion and selectivity with molybdenum substitution on vanadium sites was also observed. These results demonstrate the importance of the bulk structure on the ODH reaction. In general, propylene selectivities increased with increasing conversions at temperatures above 673 K when oxygen depletion in the reactant stream occurred. Visible and UV Raman spectroscopy corroborates this result and helps focus attention on critical surface-specific information. A new Raman peak was observed for the partially reduced MgMoO4 and is associated with a three-coordinate surface oxygen.
Original language | English (US) |
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Pages (from-to) | 419-431 |
Number of pages | 13 |
Journal | Journal of Catalysis |
Volume | 223 |
Issue number | 2 |
DOIs | |
State | Published - Apr 25 2004 |
Funding
The authors thank Erl Thorsteinson for setting up this collaboration and his helpful discussions and Richard Chaffin for the Krypton BET surface area measurements. The authors gratefully acknowledge support by the National Science Foundation and the Department of Energy under the Environmental Molecular Science Institutes program (Grant 9810378) at the Northwestern University Institute for Environmental Catalysis and made use of the Central Facilities supported by the MRSEC program of the National Science Foundation (Grant DMR-0076097) at the Materials Research Center of Northwestern University. B. Bardin acknowledges The Dow Chemical Company for support of this work.
Keywords
- Magnesium, vanadium, and molybdenum oxides
- ODH
- Oxidative dehydrogenation
- Propane
- Raman spectroscopy
ASJC Scopus subject areas
- Catalysis
- Physical and Theoretical Chemistry