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Coke Formation during Propane Dehydrogenation over Ga−Rh Supported Catalytically Active Liquid Metal Solutions
Supported Catalytically Active Liquid Metal Solutions (SCALMS) were recently described as a new class of heterogeneous catalysts, where the catalytic transformation takes place at the highly dynamic interface of a liquid alloy. Their application in alkane dehydrogenation has been claimed to be super...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7074060/ https://www.ncbi.nlm.nih.gov/pubmed/32194874 http://dx.doi.org/10.1002/cctc.201901922 |
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author | Wolf, Moritz Raman, Narayanan Taccardi, Nicola Haumann, Marco Wasserscheid, Peter |
author_facet | Wolf, Moritz Raman, Narayanan Taccardi, Nicola Haumann, Marco Wasserscheid, Peter |
author_sort | Wolf, Moritz |
collection | PubMed |
description | Supported Catalytically Active Liquid Metal Solutions (SCALMS) were recently described as a new class of heterogeneous catalysts, where the catalytic transformation takes place at the highly dynamic interface of a liquid alloy. Their application in alkane dehydrogenation has been claimed to be superior to classical heterogeneous catalysts, because the single atom nature of Rh dissolved in liquid Ga hinders the formation of significant amounts of coke, e. g. by oligomerisation of carbon fragments and excessive dehydrogenation. In the present study, we investigate the coking behaviour of Ga−Rh SCALMS during dehydrogenation of propane in detail by means of high‐resolution thermogravimetry. We report that the application of Ga−Rh SCALMS indeed limits the formation of coke when compared to the Ga‐free Rh catalyst, in particular when relating coke formation to the catalytic performance. Furthermore, the formed coke has been shown to be highly reactive during temperature programmed oxidation in 21 % O(2)/He with onset temperatures of approx. 150 °C enabling a regeneration of the Ga−Rh SCALMS system under mild conditions. The activation energy of the oxidation lies in the lower range of values reported for spent cracking catalysts. Monitoring the formation of coke and performance of SCALMS in situ via thermogravimetry coupled with mass spectrometry revealed the continuous formation of coke, which becomes the only process affecting the net weight change after a certain time on stream. |
format | Online Article Text |
id | pubmed-7074060 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-70740602020-03-17 Coke Formation during Propane Dehydrogenation over Ga−Rh Supported Catalytically Active Liquid Metal Solutions Wolf, Moritz Raman, Narayanan Taccardi, Nicola Haumann, Marco Wasserscheid, Peter ChemCatChem Full Papers Supported Catalytically Active Liquid Metal Solutions (SCALMS) were recently described as a new class of heterogeneous catalysts, where the catalytic transformation takes place at the highly dynamic interface of a liquid alloy. Their application in alkane dehydrogenation has been claimed to be superior to classical heterogeneous catalysts, because the single atom nature of Rh dissolved in liquid Ga hinders the formation of significant amounts of coke, e. g. by oligomerisation of carbon fragments and excessive dehydrogenation. In the present study, we investigate the coking behaviour of Ga−Rh SCALMS during dehydrogenation of propane in detail by means of high‐resolution thermogravimetry. We report that the application of Ga−Rh SCALMS indeed limits the formation of coke when compared to the Ga‐free Rh catalyst, in particular when relating coke formation to the catalytic performance. Furthermore, the formed coke has been shown to be highly reactive during temperature programmed oxidation in 21 % O(2)/He with onset temperatures of approx. 150 °C enabling a regeneration of the Ga−Rh SCALMS system under mild conditions. The activation energy of the oxidation lies in the lower range of values reported for spent cracking catalysts. Monitoring the formation of coke and performance of SCALMS in situ via thermogravimetry coupled with mass spectrometry revealed the continuous formation of coke, which becomes the only process affecting the net weight change after a certain time on stream. John Wiley and Sons Inc. 2020-01-07 2020-02-20 /pmc/articles/PMC7074060/ /pubmed/32194874 http://dx.doi.org/10.1002/cctc.201901922 Text en © 2019 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Full Papers Wolf, Moritz Raman, Narayanan Taccardi, Nicola Haumann, Marco Wasserscheid, Peter Coke Formation during Propane Dehydrogenation over Ga−Rh Supported Catalytically Active Liquid Metal Solutions |
title | Coke Formation during Propane Dehydrogenation over Ga−Rh Supported Catalytically Active Liquid Metal Solutions |
title_full | Coke Formation during Propane Dehydrogenation over Ga−Rh Supported Catalytically Active Liquid Metal Solutions |
title_fullStr | Coke Formation during Propane Dehydrogenation over Ga−Rh Supported Catalytically Active Liquid Metal Solutions |
title_full_unstemmed | Coke Formation during Propane Dehydrogenation over Ga−Rh Supported Catalytically Active Liquid Metal Solutions |
title_short | Coke Formation during Propane Dehydrogenation over Ga−Rh Supported Catalytically Active Liquid Metal Solutions |
title_sort | coke formation during propane dehydrogenation over ga−rh supported catalytically active liquid metal solutions |
topic | Full Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7074060/ https://www.ncbi.nlm.nih.gov/pubmed/32194874 http://dx.doi.org/10.1002/cctc.201901922 |
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