4.7 Article

Methanation of CO2 on bulk Co-Fe catalysts

Journal

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
Volume 46, Issue 76, Pages 37860-37871

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2021.09.034

Keywords

Sabatier reaction; Co-Fe catalysts; Catalyst efficiency; Surface reaction model

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The efficiency of CO2 methanation with Co-Fe catalysts was evaluated using various analytical techniques, leading to the proposal of a specific reaction mechanism with the rate-limiting step identified as the recombination of OH group in the FeOOH complex with the H atom adsorbed at the active ensemble to form H2O molecule.
The efficiency of CO2 methanation was estimated through gas chromatography in the presence of Co-Fe catalysts. Scanning electron microscopy, X-ray powder diffraction, X-ray photoelectron spectroscopy, and Moeurossbauer spectroscopy were applied for ex-situ analysis of the catalysts after their test in the methanation reaction. Thermal programmed desorption mass spectroscopy experiments were performed to identify gaseous species adsorbed at the catalyst surface. Based on the experimental results, surface reaction model of CO2 methanation on Co-Fe catalysts was proposed to specify active ensemble of metallic atoms at the catalyst surface, orientation of adsorbed CO2 molecule on the ensemble and detailed reaction mechanism of CO2/CH4 conversion. The reaction step when OH group in the FeOOH complex recombined with the H atom adsorbed at the active ensemble to form H2O molecule was considered as the rate-limiting step. (c) 2021 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.

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