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Palladium Intercalated into the Walls of Mesoporous Silica as Robust and Regenerable Catalysts for Hydrodeoxygenation of Phenolic Compounds
[Image: see text] Nanostructured noble-metal catalysts traditionally suffer from sintering under high operating temperatures, leading to durability issues and process limitations. The encapsulation of nanostructured catalysts to prevent loss of activity through thermal sintering, while maintaining a...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6644551/ https://www.ncbi.nlm.nih.gov/pubmed/31458918 http://dx.doi.org/10.1021/acsomega.8b00951 |
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author | Gage, Samuel H. Engelhardt, Jan Menart, Martin J. Ngo, Chilan Leong, G. Jeremy Ji, Yazhou Trewyn, Brian G. Pylypenko, Svitlana Richards, Ryan M. |
author_facet | Gage, Samuel H. Engelhardt, Jan Menart, Martin J. Ngo, Chilan Leong, G. Jeremy Ji, Yazhou Trewyn, Brian G. Pylypenko, Svitlana Richards, Ryan M. |
author_sort | Gage, Samuel H. |
collection | PubMed |
description | [Image: see text] Nanostructured noble-metal catalysts traditionally suffer from sintering under high operating temperatures, leading to durability issues and process limitations. The encapsulation of nanostructured catalysts to prevent loss of activity through thermal sintering, while maintaining accessibility of active sites, remains a great challenge in the catalysis community. Here, we report a robust and regenerable palladium-based catalyst, wherein palladium particles are intercalated into the three-dimensional framework of SBA-15-type mesoporous silica. The encapsulated Pd active sites remain catalytically active as demonstrated in high-temperature/pressure phenol hydrodeoxygenation reactions. The confinement of Pd particles in the walls of SBA-15 prevents particle sintering at high temperatures. Moreover, a partially deactivated catalyst containing intercalated particles is regenerated almost completely even after several reaction cycles. In contrast, Pd particles, which are not encapsulated within the SBA-15 framework, sinter and do not recover prior activity after a regeneration procedure. |
format | Online Article Text |
id | pubmed-6644551 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-66445512019-08-27 Palladium Intercalated into the Walls of Mesoporous Silica as Robust and Regenerable Catalysts for Hydrodeoxygenation of Phenolic Compounds Gage, Samuel H. Engelhardt, Jan Menart, Martin J. Ngo, Chilan Leong, G. Jeremy Ji, Yazhou Trewyn, Brian G. Pylypenko, Svitlana Richards, Ryan M. ACS Omega [Image: see text] Nanostructured noble-metal catalysts traditionally suffer from sintering under high operating temperatures, leading to durability issues and process limitations. The encapsulation of nanostructured catalysts to prevent loss of activity through thermal sintering, while maintaining accessibility of active sites, remains a great challenge in the catalysis community. Here, we report a robust and regenerable palladium-based catalyst, wherein palladium particles are intercalated into the three-dimensional framework of SBA-15-type mesoporous silica. The encapsulated Pd active sites remain catalytically active as demonstrated in high-temperature/pressure phenol hydrodeoxygenation reactions. The confinement of Pd particles in the walls of SBA-15 prevents particle sintering at high temperatures. Moreover, a partially deactivated catalyst containing intercalated particles is regenerated almost completely even after several reaction cycles. In contrast, Pd particles, which are not encapsulated within the SBA-15 framework, sinter and do not recover prior activity after a regeneration procedure. American Chemical Society 2018-07-11 /pmc/articles/PMC6644551/ /pubmed/31458918 http://dx.doi.org/10.1021/acsomega.8b00951 Text en Copyright © 2018 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Gage, Samuel H. Engelhardt, Jan Menart, Martin J. Ngo, Chilan Leong, G. Jeremy Ji, Yazhou Trewyn, Brian G. Pylypenko, Svitlana Richards, Ryan M. Palladium Intercalated into the Walls of Mesoporous Silica as Robust and Regenerable Catalysts for Hydrodeoxygenation of Phenolic Compounds |
title | Palladium Intercalated into the Walls of Mesoporous
Silica as Robust and Regenerable Catalysts for Hydrodeoxygenation
of Phenolic Compounds |
title_full | Palladium Intercalated into the Walls of Mesoporous
Silica as Robust and Regenerable Catalysts for Hydrodeoxygenation
of Phenolic Compounds |
title_fullStr | Palladium Intercalated into the Walls of Mesoporous
Silica as Robust and Regenerable Catalysts for Hydrodeoxygenation
of Phenolic Compounds |
title_full_unstemmed | Palladium Intercalated into the Walls of Mesoporous
Silica as Robust and Regenerable Catalysts for Hydrodeoxygenation
of Phenolic Compounds |
title_short | Palladium Intercalated into the Walls of Mesoporous
Silica as Robust and Regenerable Catalysts for Hydrodeoxygenation
of Phenolic Compounds |
title_sort | palladium intercalated into the walls of mesoporous
silica as robust and regenerable catalysts for hydrodeoxygenation
of phenolic compounds |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6644551/ https://www.ncbi.nlm.nih.gov/pubmed/31458918 http://dx.doi.org/10.1021/acsomega.8b00951 |
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