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Published November 8, 2007 | Supplemental Material
Journal Article Open

Mechanism of Selective Oxidation of Propene to Acrolein on Bismuth Molybdates from Quantum Mechanical Calculations

Abstract

In order to provide a basis for understanding the fundamental chemical mechanisms underlying the selective oxidation of propene to acrolein by bismuth molybdates, we report quantum mechanical studies (at the DFT/B3LYP/LACVP^(**) level) of various reaction steps on bismuth oxide (Bi_4O_6/Bi_4O_7) and molybdenum oxide (Mo_3O_9) cluster models. For CH activation, we find a low-energy pathway on a Bi^V site with a calculated barrier of ΔH^⧧ = 11.0 kcal/mol (ΔG^⧧ = 30.4 kcal/mol), which is ∼3 kcal/mol lower than the experimentally measured barrier on a pure Bi_2O_3 condensed phase. We find this process to be not feasible on Bi^(III) (it is highly endothermic, ΔE = 50.9 kcal/mol, ΔG = 41.6 kcal/mol) or on pure molybdenum oxide (prohibitively high barriers, ΔE^⧧ = 32.5 kcal/mol, ΔG^⧧ = 48.1 kcal/mol), suggesting that the CH activation event occurs on (rare) Bi^V sites on the Bi_2O_3 surface. The expected low concentration of Bi^V could explain the 3 kcal/mol discrepancy between our calculated barrier and experiment. We present in detail the allyl oxidation mechanism over Mo_3O_9, which includes the adsorption of allyl to form the π-allyl and σ-allyl species, the second hydrogen abstraction to form acrolein, and acrolein desorption. The formation of σ-allyl intermediate is reversible, with forward ΔE^⧧ (ΔG^⧧) barriers of 2.7 (9.0 with respect to the π-allyl intermediate) kcal/mol and reverse barriers of 21.6 (23.7) kcal/mol. The second hydrogen abstraction is the rate-determining step for allyl conversion, with a calculated ΔE^⧧ = 35.6 kcal/mol (ΔG^⧧ = 37.5 kcal/mol). Finally, studies of acrolein desorption in presence of gaseous O_2 suggest that the reoxidation significantly weakens the coordination of acrolein to the reduced MoIV site, helping drive desorption of acrolein from the surface.

Additional Information

© 2007 American Chemical Society. Received 8 June 2007. Published online 11 October 2007. Published in print 1 November 2007. The personnel involved in this research were partially supported by DOE (DE-PS36-03GO93015), ONR (N00014-06-1-0938), and Chevron. The facilities were supported by ARO-DURIP and ONR-DURIP funds.

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August 19, 2023
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