Mechanism of oxidation of allyl alcohol on a V-Mo oxide catalyst
The kinetics of oxidation of allyl alcohol by oxygen on a V-Mo oxide catalyst have been studied in situ by EPR. It has been found that during the course of the reaction V ions within the bulk volume of the catalyst undergo redox conversions, V/sup 4+/ /yields/ V/sup 5+/. At elevated temperatures (213/degree/C) the process kinetics can be described very well in terms of an oxidation-reduction scheme which takes into account reactions occurring within the catalyst bulk, and that the rate of acrolein formation is linearly related to the concentration (V/sup 4+/) in the catalyst volume. At lower temperatures this relationship is disrupted, and the rate of acrolein formation is no longer dependent on the O/sub 2/ pressure. In order to account for these effects the authors have proposed a stepwise scheme, which incorporates an oxygen activation step.
- Research Organization:
- Institute of Chemical Physics, Moscow (USSR)
- OSTI ID:
- 6009084
- Journal Information:
- Kinet. Catal. (Engl. Transl.); (United States), Vol. 29:4; Other Information: Translated from Kinet. Katal.; 29: No. 4, 876-879 (Jul-Aug 1988)
- Country of Publication:
- United States
- Language:
- English
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Related Subjects
ORGANIC
PHYSICAL AND ANALYTICAL CHEMISTRY
ALCOHOLS
OXIDATION
CATALYSTS
ELECTRON SPIN RESONANCE
MOLYBDENUM OXIDES
CATALYTIC EFFECTS
VANADIUM
ACROLEIN
CATALYSIS
CHEMICAL REACTION KINETICS
CHEMICAL REACTION YIELD
DEACTIVATION
KINETIC EQUATIONS
MATHEMATICAL MODELS
REDOX POTENTIAL
REDOX REACTIONS
REDUCTION
TEMPERATURE DEPENDENCE
VALENCE
ALDEHYDES
CHALCOGENIDES
CHEMICAL REACTIONS
ELEMENTS
EQUATIONS
HYDROXY COMPOUNDS
KINETICS
MAGNETIC RESONANCE
METALS
MOLYBDENUM COMPOUNDS
ORGANIC COMPOUNDS
OXIDES
OXYGEN COMPOUNDS
REACTION KINETICS
REFRACTORY METAL COMPOUNDS
RESONANCE
TRANSITION ELEMENT COMPOUNDS
TRANSITION ELEMENTS
YIELDS
400201* - Chemical & Physicochemical Properties