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Multi-walled carbon nanotube-based composite materials as catalyst support for water–gas shift and hydroformylation reactions

In times of depleting fossil fuel reserves, optimizing industrial catalytic reactions has become increasingly important. One possibility for optimization is the use of homogenous catalysts, which are advantageous over heterogeneous catalysts because of mild reaction conditions as well as higher sele...

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Autores principales: Wolf, Patrick, Logemann, Morten, Schörner, Markus, Keller, Laura, Haumann, Marco, Wessling, Matthias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9070777/
https://www.ncbi.nlm.nih.gov/pubmed/35529233
http://dx.doi.org/10.1039/c9ra04830h
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author Wolf, Patrick
Logemann, Morten
Schörner, Markus
Keller, Laura
Haumann, Marco
Wessling, Matthias
author_facet Wolf, Patrick
Logemann, Morten
Schörner, Markus
Keller, Laura
Haumann, Marco
Wessling, Matthias
author_sort Wolf, Patrick
collection PubMed
description In times of depleting fossil fuel reserves, optimizing industrial catalytic reactions has become increasingly important. One possibility for optimization is the use of homogenous catalysts, which are advantageous over heterogeneous catalysts because of mild reaction conditions as well as higher selectivity and activity. A new emerging technology, supported ionic liquid phase (SILP), was developed to permanently immobilize homogeneous catalyst complexes for continuous processes. However, these SILP catalysts are unable to form freestanding supports by themselves. This study presents a new method to introduce the SILP system into a support made from multi-walled carbon nanotubes (MWCNT). In a first step, SILP catalysts were prepared for hydroformylation as well as low-temperature water–gas shift (WGS) reactions. These catalysts were integrated into freestanding microtubes formed from MWCNTs, with silica (for hydroformylation) or alumina particles (for WGS) incorporated. In hydroformylation, the activity increased significantly by around 400% when the pure MWCNT material was used as SILP support. An opposite trend was observed for WGS, where pure alumina particles exhibited the highest activity. A significant advantage of the MWCNT composite materials is the possibility to coat them with separation layers, which allows their application in membrane reactors for more efficient processes.
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spelling pubmed-90707772022-05-06 Multi-walled carbon nanotube-based composite materials as catalyst support for water–gas shift and hydroformylation reactions Wolf, Patrick Logemann, Morten Schörner, Markus Keller, Laura Haumann, Marco Wessling, Matthias RSC Adv Chemistry In times of depleting fossil fuel reserves, optimizing industrial catalytic reactions has become increasingly important. One possibility for optimization is the use of homogenous catalysts, which are advantageous over heterogeneous catalysts because of mild reaction conditions as well as higher selectivity and activity. A new emerging technology, supported ionic liquid phase (SILP), was developed to permanently immobilize homogeneous catalyst complexes for continuous processes. However, these SILP catalysts are unable to form freestanding supports by themselves. This study presents a new method to introduce the SILP system into a support made from multi-walled carbon nanotubes (MWCNT). In a first step, SILP catalysts were prepared for hydroformylation as well as low-temperature water–gas shift (WGS) reactions. These catalysts were integrated into freestanding microtubes formed from MWCNTs, with silica (for hydroformylation) or alumina particles (for WGS) incorporated. In hydroformylation, the activity increased significantly by around 400% when the pure MWCNT material was used as SILP support. An opposite trend was observed for WGS, where pure alumina particles exhibited the highest activity. A significant advantage of the MWCNT composite materials is the possibility to coat them with separation layers, which allows their application in membrane reactors for more efficient processes. The Royal Society of Chemistry 2019-09-03 /pmc/articles/PMC9070777/ /pubmed/35529233 http://dx.doi.org/10.1039/c9ra04830h Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Wolf, Patrick
Logemann, Morten
Schörner, Markus
Keller, Laura
Haumann, Marco
Wessling, Matthias
Multi-walled carbon nanotube-based composite materials as catalyst support for water–gas shift and hydroformylation reactions
title Multi-walled carbon nanotube-based composite materials as catalyst support for water–gas shift and hydroformylation reactions
title_full Multi-walled carbon nanotube-based composite materials as catalyst support for water–gas shift and hydroformylation reactions
title_fullStr Multi-walled carbon nanotube-based composite materials as catalyst support for water–gas shift and hydroformylation reactions
title_full_unstemmed Multi-walled carbon nanotube-based composite materials as catalyst support for water–gas shift and hydroformylation reactions
title_short Multi-walled carbon nanotube-based composite materials as catalyst support for water–gas shift and hydroformylation reactions
title_sort multi-walled carbon nanotube-based composite materials as catalyst support for water–gas shift and hydroformylation reactions
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9070777/
https://www.ncbi.nlm.nih.gov/pubmed/35529233
http://dx.doi.org/10.1039/c9ra04830h
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