Chalachew Mebrahtu
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
Authors
Florian Krebs
Gianfranco Giorgianni
Salvatore Abate
Siglinda Perathoner
Gabriele Centi
Alexander I. Large
Georg Held
Dr Rosa Arrigo R.Arrigo@salford.ac.uk
Associate Professor/Reader
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. |
Files
Published Version
(8.9 Mb)
PDF
You might also like
Alkali Containing Layered Metal Oxides as Catalysts for the Oxygen Evolution Reaction
(2024)
Journal Article
Assessment of the Degradation Mechanisms of Cu Electrodes during the CO
(2023)
Journal Article
Downloadable Citations
About USIR
Administrator e-mail: library-research@salford.ac.uk
This application uses the following open-source libraries:
SheetJS Community Edition
Apache License Version 2.0 (http://www.apache.org/licenses/)
PDF.js
Apache License Version 2.0 (http://www.apache.org/licenses/)
Font Awesome
SIL OFL 1.1 (http://scripts.sil.org/OFL)
MIT License (http://opensource.org/licenses/mit-license.html)
CC BY 3.0 ( http://creativecommons.org/licenses/by/3.0/)
Powered by Worktribe © 2024
Advanced Search