Key Words:OXIDE CATALYSTS; STABILITY; ETHANE

Abstract:The chemical looping oxidative dehydrogenation of propane to propylene (CL-ODHP) replaces molecular oxygen with lattice oxygen (O-latt) in oxygen carriers. This method boosts propylene selectivity by avoiding the deep oxidation of propane. Herein, a series of 10V-XCe/Al oxygen carriers with different Ce contents were prepared to realize different VOx-CeOy interactions. The effect of the Ce content in 10V-XCe/Al oxygen carriers on the CL-ODHP reaction was studied and the optimal Ce content was determined. CeO2 prevents the outward diffusion and evolution of O-latt in VOx carriers to the adsorbed electrophilic oxygen species (O-elec), effectively inhibiting the loss of O-latt, improving the selectivity of propylene, and extending the lifetime and activity of the oxygen carriers. After characterizing and analyzing the oxygen carriers, it was found that 10V-3Ce/Al has the highest specific surface area, highest oxygen capacity, and lowest reducibility. The 10V-3Ce/Al also delivers the highest oxidative dehydrogenation performance. At 550 ?, the average propylene and COx selectivity values of 10V-3Ce/Al were 81.87% and 7.28%, respectively (vs. 62.79% and 25.64% respectively, for 10V/Al). It is demonstrated that 10V-3Ce/Al exhibits good cycle stability with no significant decrease in catalytic performance after 15 cycles. In situ diffuse-reflectance infrared Fourier-transform spectroscopy indicates that CL-ODHP on 10V-3Ce/Al undergoes the Mars-van Krevelen mechanism. The migration and evolution of O-latt in oxygen carriers is controlled by reasonably modifying the metal oxide interactions to improve propylene yield. This work will thus guide the subsequent development of novel and efficient CL-ODHP oxygen carriers.

Volume:13

Issue:5

Translation or Not:no