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|Title: ||Elucidating the role of CO2 in the soft oxidative dehydrogenation of propane over ceria-based catalysts|
|Authors: ||Nowicka, Ewa|
Althahban, Sultan M.
Mohammed, Khaled M.
Kondrat, Simon A.
Morgan, David J.
Willock, David J.
Kiely, Christopher J.
Hutchings, Graham J.
Propane oxidative dehydrogenation
Reverse water-gas shift
|Issue Date: ||2018|
|Publisher: ||© American Chemical Society|
|Citation: ||NOWICKA, E. ... et al, 2018. Elucidating the role of CO2 in the soft oxidative dehydrogenation of propane over ceria-based catalysts. ACS Catalysis, 8 (4), pp.3454-3468.|
|Abstract: ||A mixed oxide support containing Ce, Zr, and Al was synthesized using a physical grinding method and applied in the oxidative dehydrogenation of propane using CO 2 as the oxidant. The activity of the support was compared with that of fully formulated catalysts containing palladium. The Pd/CeZrAlO x material exhibited long-term stability and selectivity to propene (during continuous operation for 140 h), which is not normally associated with dehydrogenation catalysts. From temperature-programmed desorption of NH 3 and CO 2 it was found that the catalyst possessed both acidic and basic sites. In addition, temperature-programmed reduction showed that palladium promoted both the reduction and reoxidation of the support. When the role of CO 2 was investigated in the absence of gas-phase oxidant, using a temporal analysis of products (TAP) reactor, it was found that CO 2 dissociates over the reduced catalyst, leading to formation of CO and selective oxygen species. It is proposed that CO 2 has the dual role of regenerating selective oxygen species and shifting the equilibrium for alkane dehydrogenation by consuming H 2 through the reverse water-gas-shift reaction. These two mechanistic functions have previously been considered to be mutually exclusive.|
|Description: ||This paper is closed access until 13 March 2019.|
|Sponsor: ||This work was funded by the European Research Council, through the following grant: After the Goldrush, ERC-AG-291319. C.J.K. gratefully acknowledges funding from the National Science Foundation Major Research Instrumentation program (GR# MRI/DMR-1040229). We thank Diamond Light Source for use of B18 (SP8071-12), with gratitude to Dr. Diego Gianolio. E.N. thanks the Technical University of Berlin and Marie Curie-Sklodowska Action for awarding her IPODI fellowship.|
|Version: ||Accepted for publication|
|Publisher Link: ||https://doi.org/10.1021/acscatal.7b03805|
|Appears in Collections:||Closed Access (Chemistry)|
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