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Insights by in-situ studies on the nature of highly-active hydrotalcite-based Ni-Fe catalysts for CO2 methanation

Mebrahtu, Chalachew; Krebs, Florian; Giorgianni, Gianfranco; Abate, Salvatore; Perathoner, Siglinda; Centi, Gabriele; Large, Alexander I.; Held, Georg; Arrigo, Rosa; Palkovits, Regina

Insights by in-situ studies on the nature of highly-active hydrotalcite-based Ni-Fe catalysts for CO2 methanation Thumbnail


Authors

Chalachew Mebrahtu

Florian Krebs

Gianfranco Giorgianni

Salvatore Abate

Siglinda Perathoner

Gabriele Centi

Alexander I. Large

Georg Held

Regina Palkovits



Abstract

Designing CO2 methanation catalysts that meet industrial requirements is still challenging. We report Ni-Fe hydrotalcite-derived catalysts with a wide range of Ni and Mg loadings showing that an optimised composition with Ni0.4 gives a very high CO2 conversion rate of 0.37 mmol/gcat/s at 300 °C. This catalyst is studied by in-situ APXPS and NEXAFS spectroscopies and compared with the other synthesised samples to obtain new mechanistic insights on methanation catalysts active for low-temperature (300 °C) methanation, which is an industrial requirement. Under methanation conditions, in-situ investigations revealed the presence of metallic Ni sites and low nuclearity Ni-Fe species at (Ni loading) = 21.2 mol%. These sites are oxidised on the low Ni-loaded catalyst (= 9.2 mol%). The best CO2 conversion rate and CH4 selectivity are shown at intermediate (21.2 mol%), in the presence of Mg. These superior performances are related to the high metallic surface area, dispersion, and optimal density of basic sites. The (turnover frequency of CO2 conversion) increases exponentially with the fractional density of basic to metallic sites () from 1.1 s-1 (= 29.2 mol%) to 9.1 s-1 (= 7.6 mol%). It follows the opposite trend of the CO2 conversion rate. In-situ DRIFTS data under methanation conditions evidence that the at high is related to the presence of a formate route which is not predominant at low (high ). A synergistic interplay of basic and metallic sites is present. This contribution provides a rationale for designing industrially competitive CO2 methanation catalysts with high catalytic activity while maintaining low Ni loading.

Citation

Mebrahtu, C., Krebs, F., Giorgianni, G., Abate, S., Perathoner, S., Centi, G., …Palkovits, R. (2023). Insights by in-situ studies on the nature of highly-active hydrotalcite-based Ni-Fe catalysts for CO2 methanation. Chemical Engineering Research and Design, 193, 320-339. https://doi.org/10.1016/j.cherd.2023.03.026

Journal Article Type Article
Acceptance Date Mar 14, 2023
Online Publication Date Mar 17, 2023
Publication Date Apr 4, 2023
Deposit Date Sep 16, 2024
Publicly Available Date Sep 17, 2024
Journal Chemical Engineering Research and Design
Print ISSN 0263-8762
Electronic ISSN 1744-3563
Publisher Elsevier
Peer Reviewed Peer Reviewed
Volume 193
Pages 320-339
DOI https://doi.org/10.1016/j.cherd.2023.03.026
Additional Information This article is maintained by: Elsevier; Article Title: Insights by in-situ studies on the nature of highly-active hydrotalcite-based Ni-Fe catalysts for CO2 methanation; Journal Title: Chemical Engineering Research and Design; CrossRef DOI link to publisher maintained version: https://doi.org/10.1016/j.cherd.2023.03.026; Content Type: article; Copyright: © 2023 The Authors. Published by Elsevier Ltd on behalf of Institution of Chemical Engineers.

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