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Highly Active Ce- and Mg-Promoted Ni Catalysts Supported on Cellulose-Derived Carbon for Low-Temperature CO(2) Methanation
[Image: see text] The CO(2) methanation performance of Mg- and/or Ce-promoted Ni catalysts supported on cellulose-derived carbon (CDC) was investigated. The samples, prepared by biomorphic mineralization techniques, exhibit pore distributions correlated to the particle sizes, revealing a direct effe...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9161724/ https://www.ncbi.nlm.nih.gov/pubmed/35663907 http://dx.doi.org/10.1021/acs.energyfuels.1c01682 |
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author | Tarifa, Pilar Megías-Sayago, Cristina Cazaña, Fernando González-Martín, Miguel Latorre, Nieves Romeo, Eva Delgado, Juan José Monzón, Antonio |
author_facet | Tarifa, Pilar Megías-Sayago, Cristina Cazaña, Fernando González-Martín, Miguel Latorre, Nieves Romeo, Eva Delgado, Juan José Monzón, Antonio |
author_sort | Tarifa, Pilar |
collection | PubMed |
description | [Image: see text] The CO(2) methanation performance of Mg- and/or Ce-promoted Ni catalysts supported on cellulose-derived carbon (CDC) was investigated. The samples, prepared by biomorphic mineralization techniques, exhibit pore distributions correlated to the particle sizes, revealing a direct effect of the metal content in the textural properties of the samples. The catalytic performance, evaluated as CO(2) conversion and CH(4) selectivity, reveals that Ce is a better promoter than Mg, reaching higher conversion values in all of the studied temperature range (150–500 °C). In the interval of 350–400 °C, Ni–Mg–Ce/CDC attains the maximum yield to methane, 80%, reaching near 100% CH(4) selectivity. Ce-promoted catalysts were highly active at low temperatures (175 °C), achieving 54% CO(2) conversion with near 100% CH(4) selectivity. Furthermore, the large potential stability of the Ni–Mg–Ce/CDC catalyst during consecutive cycles of reaction opens a promising route for the optimization of the Sabatier process using this type of catalyst. |
format | Online Article Text |
id | pubmed-9161724 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-91617242022-06-03 Highly Active Ce- and Mg-Promoted Ni Catalysts Supported on Cellulose-Derived Carbon for Low-Temperature CO(2) Methanation Tarifa, Pilar Megías-Sayago, Cristina Cazaña, Fernando González-Martín, Miguel Latorre, Nieves Romeo, Eva Delgado, Juan José Monzón, Antonio Energy Fuels [Image: see text] The CO(2) methanation performance of Mg- and/or Ce-promoted Ni catalysts supported on cellulose-derived carbon (CDC) was investigated. The samples, prepared by biomorphic mineralization techniques, exhibit pore distributions correlated to the particle sizes, revealing a direct effect of the metal content in the textural properties of the samples. The catalytic performance, evaluated as CO(2) conversion and CH(4) selectivity, reveals that Ce is a better promoter than Mg, reaching higher conversion values in all of the studied temperature range (150–500 °C). In the interval of 350–400 °C, Ni–Mg–Ce/CDC attains the maximum yield to methane, 80%, reaching near 100% CH(4) selectivity. Ce-promoted catalysts were highly active at low temperatures (175 °C), achieving 54% CO(2) conversion with near 100% CH(4) selectivity. Furthermore, the large potential stability of the Ni–Mg–Ce/CDC catalyst during consecutive cycles of reaction opens a promising route for the optimization of the Sabatier process using this type of catalyst. American Chemical Society 2021-09-01 2021-11-04 /pmc/articles/PMC9161724/ /pubmed/35663907 http://dx.doi.org/10.1021/acs.energyfuels.1c01682 Text en © 2021 American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Tarifa, Pilar Megías-Sayago, Cristina Cazaña, Fernando González-Martín, Miguel Latorre, Nieves Romeo, Eva Delgado, Juan José Monzón, Antonio Highly Active Ce- and Mg-Promoted Ni Catalysts Supported on Cellulose-Derived Carbon for Low-Temperature CO(2) Methanation |
title | Highly Active Ce- and Mg-Promoted Ni Catalysts Supported
on Cellulose-Derived Carbon for Low-Temperature CO(2) Methanation |
title_full | Highly Active Ce- and Mg-Promoted Ni Catalysts Supported
on Cellulose-Derived Carbon for Low-Temperature CO(2) Methanation |
title_fullStr | Highly Active Ce- and Mg-Promoted Ni Catalysts Supported
on Cellulose-Derived Carbon for Low-Temperature CO(2) Methanation |
title_full_unstemmed | Highly Active Ce- and Mg-Promoted Ni Catalysts Supported
on Cellulose-Derived Carbon for Low-Temperature CO(2) Methanation |
title_short | Highly Active Ce- and Mg-Promoted Ni Catalysts Supported
on Cellulose-Derived Carbon for Low-Temperature CO(2) Methanation |
title_sort | highly active ce- and mg-promoted ni catalysts supported
on cellulose-derived carbon for low-temperature co(2) methanation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9161724/ https://www.ncbi.nlm.nih.gov/pubmed/35663907 http://dx.doi.org/10.1021/acs.energyfuels.1c01682 |
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