The Influence of Melting on Catalysis in Propane Oxidation

Author:

Erdem Ezgi12,Tarasov Andrey V.1,Kube Pierre1,Koch Gregor1,Plodinec Milivoj1,Lunkenbein Thomas1,Carey Spencer1,Wang Yuanqing1,Hävecker Michael13,Rosowski Frank24,Schlögl Robert1,Trunschke Annette1ORCID

Affiliation:

1. Department of Inorganic Chemistry Fritz-Haber-Institute der Max-Planck-Gesellschaft Faradayweg 4–6 14195 Berlin Germany

2. BasCat-UniCat BASF JointLab Technical University Berlin Sekr. EW K 01, Hardenbergstrasse 36 10623 Berlin Germany

3. Max Planck Institute for Chemical Energy Conversion, postCode/>45470 Mülheim Germany

4. BASF SE Catalysis Research Carl-Bosch-Strasse 38 67056 Ludwigshafen Germany

Abstract

AbstractA model catalyst composed of crystalline potassium pentavanadate (K3V5O14) supported on silica was studied to elucidate the effect of phase transitions on the performance of potassium‐promoted vanadia catalysts in propane oxidation. Operando calorimetry shows a clear correlation between a drop in activity and an increase in selectivity to propylene upon melting of the crystalline K3V5O14 phase under reaction conditions. The pentavanadate phase itself is not active in propane oxidation, neither in the solid nor in the molten state. The activity of the catalyst mainly originates from highly‐active, i. e., unselective VxOy surface species anchored to silica and formed during synthesis in addition to the supported pentavanadate phase. Melting of K3V5O14 leads to the coverage of these VxOy species preventing the overoxidation of propylene and leading to an increase in propylene selectivity. The change in catalyst properties is therefore due to a physical effect and not to a change in the chemical properties of the predominant crystalline phase.

Publisher

Wiley

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

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