4.7 Article

Double perovskite type catalysts with improved anti-coking and sulfur-resisting performance for diesel reforming

期刊

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
卷 48, 期 27, 页码 9929-9944

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2022.11.310

关键词

Double perovskites; Sol-gel method; Diesel reforming; Sulfur resisting; Anti-coking

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Double perovskite type catalysts with the formula of La2CoxFe2-xO5+d (x = 1.5, 1 and 0.5) were synthesized via a modified sol-gel method, and showed improved anti-coking and sulfur-resisting performance for steam reforming of n-hexadecane. Characterizations revealed that the special structure of double perovskite minimized coke formation and improved sulfur resisting, due to the generation of oxygen vacancies. The molar ratio of Co to Fe also had an effect on catalyst activity, and the catalyst LCF-2 (for x = 1) with a porous structure exhibited the best catalytic activity and stability.
Double perovskite type catalysts with the formula of La2CoxFe2-xO5+d, x = 1.5, 1 and 0.5 were synthesized through a modified sol-gel method, which were used for steam reforming of n-hexadecane (a diesel surrogate) containing 50 mg/g sulfur. The prepared catalysts were found to have the significantly improved performance in both anti-coking and sulfur -resisting. Characterizations with XRD, SEM-EDS, XPS, H2-TPR, thermogravimetric anal-ysis (TGA) and nitrogen adsorption-desorption revealed that the special structure of double perovskite minimized coke formation and improved sulfur resisting, as more oxygen vacancies are generated due to the consumption of surface oxygen, which provides an efficient channel for oxygen diffusion. The effect of different molar ratios of Co to Fe on catalyst activity was also studied, and the catalyst LCF-2 (for x = 1) with a porous structure had the best catalytic activity and stability, achieving a continuous runtime of more than 40 h, better than the single perovskite catalyst LaCo0.5Fe0.5O3.(c) 2022 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.

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