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Improving the Performance of Supported Ionic Liquid Phase Catalysts for the Ultra-Low-Temperature Water Gas Shift Reaction Using Organic Salt Additives
[Image: see text] The water gas shift reaction (WGSR) is catalyzed by supported ionic liquid phase (SILP) systems containing homogeneous Ru complexes dissolved in ionic liquids (ILs). These systems work at very low temperatures, that is, between 120 and 160 °C, as compared to >200 °C in the conve...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9088848/ https://www.ncbi.nlm.nih.gov/pubmed/35572184 http://dx.doi.org/10.1021/acscatal.1c05979 |
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author | Wolf, Patrick Wick, Christian R. Mehler, Julian Blaumeiser, Dominik Schötz, Simon Bauer, Tanja Libuda, Jörg Smith, David Smith, Ana-Sunčana Haumann, Marco |
author_facet | Wolf, Patrick Wick, Christian R. Mehler, Julian Blaumeiser, Dominik Schötz, Simon Bauer, Tanja Libuda, Jörg Smith, David Smith, Ana-Sunčana Haumann, Marco |
author_sort | Wolf, Patrick |
collection | PubMed |
description | [Image: see text] The water gas shift reaction (WGSR) is catalyzed by supported ionic liquid phase (SILP) systems containing homogeneous Ru complexes dissolved in ionic liquids (ILs). These systems work at very low temperatures, that is, between 120 and 160 °C, as compared to >200 °C in the conventional process. To improve the performance of this ultra-low-temperature catalysis, we investigated the influence of various additives on the catalytic activity of these SILP systems. In particular, the application of methylene blue (MB) as an additive doubled the activity. Infrared spectroscopy measurements combined with density functional theory (DFT) calculations excluded a coordinative interaction of MB with the Ru complex. In contrast, state-of-the-art theoretical calculations elucidated the catalytic effect of the additives by non-covalent interactions. In particular, the additives can significantly lower the barrier of the rate-determining step of the reaction mechanism via formation of hydrogen bonds. The theoretical predictions, thereby, showed excellent agreement with the increase of experimental activity upon variation of the hydrogen bonding moieties in the additives investigated. |
format | Online Article Text |
id | pubmed-9088848 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-90888482023-04-27 Improving the Performance of Supported Ionic Liquid Phase Catalysts for the Ultra-Low-Temperature Water Gas Shift Reaction Using Organic Salt Additives Wolf, Patrick Wick, Christian R. Mehler, Julian Blaumeiser, Dominik Schötz, Simon Bauer, Tanja Libuda, Jörg Smith, David Smith, Ana-Sunčana Haumann, Marco ACS Catal [Image: see text] The water gas shift reaction (WGSR) is catalyzed by supported ionic liquid phase (SILP) systems containing homogeneous Ru complexes dissolved in ionic liquids (ILs). These systems work at very low temperatures, that is, between 120 and 160 °C, as compared to >200 °C in the conventional process. To improve the performance of this ultra-low-temperature catalysis, we investigated the influence of various additives on the catalytic activity of these SILP systems. In particular, the application of methylene blue (MB) as an additive doubled the activity. Infrared spectroscopy measurements combined with density functional theory (DFT) calculations excluded a coordinative interaction of MB with the Ru complex. In contrast, state-of-the-art theoretical calculations elucidated the catalytic effect of the additives by non-covalent interactions. In particular, the additives can significantly lower the barrier of the rate-determining step of the reaction mechanism via formation of hydrogen bonds. The theoretical predictions, thereby, showed excellent agreement with the increase of experimental activity upon variation of the hydrogen bonding moieties in the additives investigated. American Chemical Society 2022-04-27 2022-05-06 /pmc/articles/PMC9088848/ /pubmed/35572184 http://dx.doi.org/10.1021/acscatal.1c05979 Text en © 2022 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 | Wolf, Patrick Wick, Christian R. Mehler, Julian Blaumeiser, Dominik Schötz, Simon Bauer, Tanja Libuda, Jörg Smith, David Smith, Ana-Sunčana Haumann, Marco Improving the Performance of Supported Ionic Liquid Phase Catalysts for the Ultra-Low-Temperature Water Gas Shift Reaction Using Organic Salt Additives |
title | Improving the Performance of Supported Ionic Liquid
Phase Catalysts for the Ultra-Low-Temperature Water Gas Shift Reaction
Using Organic Salt Additives |
title_full | Improving the Performance of Supported Ionic Liquid
Phase Catalysts for the Ultra-Low-Temperature Water Gas Shift Reaction
Using Organic Salt Additives |
title_fullStr | Improving the Performance of Supported Ionic Liquid
Phase Catalysts for the Ultra-Low-Temperature Water Gas Shift Reaction
Using Organic Salt Additives |
title_full_unstemmed | Improving the Performance of Supported Ionic Liquid
Phase Catalysts for the Ultra-Low-Temperature Water Gas Shift Reaction
Using Organic Salt Additives |
title_short | Improving the Performance of Supported Ionic Liquid
Phase Catalysts for the Ultra-Low-Temperature Water Gas Shift Reaction
Using Organic Salt Additives |
title_sort | improving the performance of supported ionic liquid
phase catalysts for the ultra-low-temperature water gas shift reaction
using organic salt additives |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9088848/ https://www.ncbi.nlm.nih.gov/pubmed/35572184 http://dx.doi.org/10.1021/acscatal.1c05979 |
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