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GaPt Supported Catalytically Active Liquid Metal Solution Catalysis for Propane Dehydrogenation–Support Influence and Coking Studies
[Image: see text] Supported catalytically active liquid metal solutions (SCALMS) of Pt in Ga (2 at.-% Pt) were studied in the temperature range of 500 to 600 °C for propane dehydrogenation. A facile synthesis procedure using ultrasonication was implemented and compared to a previously reported organ...
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/PMC8576810/ https://www.ncbi.nlm.nih.gov/pubmed/34777909 http://dx.doi.org/10.1021/acscatal.1c01924 |
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author | Raman, Narayanan Wolf, Moritz Heller, Martina Heene-Würl, Nina Taccardi, Nicola Haumann, Marco Felfer, Peter Wasserscheid, Peter |
author_facet | Raman, Narayanan Wolf, Moritz Heller, Martina Heene-Würl, Nina Taccardi, Nicola Haumann, Marco Felfer, Peter Wasserscheid, Peter |
author_sort | Raman, Narayanan |
collection | PubMed |
description | [Image: see text] Supported catalytically active liquid metal solutions (SCALMS) of Pt in Ga (2 at.-% Pt) were studied in the temperature range of 500 to 600 °C for propane dehydrogenation. A facile synthesis procedure using ultrasonication was implemented and compared to a previously reported organo-chemical route for gallium deposition. The procedure was applied to synthesize GaPt-SCALMS catalyst on silica (SiO(2)), alumina (Al(2)O(3)), and silicon carbide (SiC) to investigate the effect of the support material on the catalytic performance. The SiC-based SCALMS catalyst showed the highest activity, while SiO(2)-based SCALMS showed the highest stability and lowest cracking tendency at higher temperatures. The selectivity toward propene for the SiO(2)-based catalyst remained above 93% at 600 °C. The catalysts were analyzed for coke content after use by temperature-programmed oxidation (TPO) and Raman spectroscopy. While the SiC- and SiO(2)-supported SCALMS systems showed hardly any coke formation, the Al(2)O(3)-supported systems suffered from pronounced coking. SEM-EDX analyses of the catalysts before and after reaction indicated that no perceivable morphological changes occur during reaction. The SCALMS catalysts under investigation are compared with supported Pt and supported GaPt solid-phase catalyst, and possible deactivation pathways are discussed. |
format | Online Article Text |
id | pubmed-8576810 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-85768102021-11-10 GaPt Supported Catalytically Active Liquid Metal Solution Catalysis for Propane Dehydrogenation–Support Influence and Coking Studies Raman, Narayanan Wolf, Moritz Heller, Martina Heene-Würl, Nina Taccardi, Nicola Haumann, Marco Felfer, Peter Wasserscheid, Peter ACS Catal [Image: see text] Supported catalytically active liquid metal solutions (SCALMS) of Pt in Ga (2 at.-% Pt) were studied in the temperature range of 500 to 600 °C for propane dehydrogenation. A facile synthesis procedure using ultrasonication was implemented and compared to a previously reported organo-chemical route for gallium deposition. The procedure was applied to synthesize GaPt-SCALMS catalyst on silica (SiO(2)), alumina (Al(2)O(3)), and silicon carbide (SiC) to investigate the effect of the support material on the catalytic performance. The SiC-based SCALMS catalyst showed the highest activity, while SiO(2)-based SCALMS showed the highest stability and lowest cracking tendency at higher temperatures. The selectivity toward propene for the SiO(2)-based catalyst remained above 93% at 600 °C. The catalysts were analyzed for coke content after use by temperature-programmed oxidation (TPO) and Raman spectroscopy. While the SiC- and SiO(2)-supported SCALMS systems showed hardly any coke formation, the Al(2)O(3)-supported systems suffered from pronounced coking. SEM-EDX analyses of the catalysts before and after reaction indicated that no perceivable morphological changes occur during reaction. The SCALMS catalysts under investigation are compared with supported Pt and supported GaPt solid-phase catalyst, and possible deactivation pathways are discussed. American Chemical Society 2021-10-21 2021-11-05 /pmc/articles/PMC8576810/ /pubmed/34777909 http://dx.doi.org/10.1021/acscatal.1c01924 Text en © 2021 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Raman, Narayanan Wolf, Moritz Heller, Martina Heene-Würl, Nina Taccardi, Nicola Haumann, Marco Felfer, Peter Wasserscheid, Peter GaPt Supported Catalytically Active Liquid Metal Solution Catalysis for Propane Dehydrogenation–Support Influence and Coking Studies |
title | GaPt Supported Catalytically Active Liquid Metal Solution
Catalysis for Propane Dehydrogenation–Support Influence and
Coking Studies |
title_full | GaPt Supported Catalytically Active Liquid Metal Solution
Catalysis for Propane Dehydrogenation–Support Influence and
Coking Studies |
title_fullStr | GaPt Supported Catalytically Active Liquid Metal Solution
Catalysis for Propane Dehydrogenation–Support Influence and
Coking Studies |
title_full_unstemmed | GaPt Supported Catalytically Active Liquid Metal Solution
Catalysis for Propane Dehydrogenation–Support Influence and
Coking Studies |
title_short | GaPt Supported Catalytically Active Liquid Metal Solution
Catalysis for Propane Dehydrogenation–Support Influence and
Coking Studies |
title_sort | gapt supported catalytically active liquid metal solution
catalysis for propane dehydrogenation–support influence and
coking studies |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8576810/ https://www.ncbi.nlm.nih.gov/pubmed/34777909 http://dx.doi.org/10.1021/acscatal.1c01924 |
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