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Catalytic conversion of glucose to 5-hydroxymethylfurfural using zirconium-containing metal–organic frameworks using microwave heating
5-Hydroxymethylfurfural (5-HMF) can be prepared by the catalytic dehydration of glucose or fructose using a range of homogeneous or heterogeneous catalysts. For our research, a selection of closely related Metal–Organic Frameworks (MOFs) were used as catalysts in the conversion of glucose to 5-HMF d...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9085719/ https://www.ncbi.nlm.nih.gov/pubmed/35548202 http://dx.doi.org/10.1039/c8ra06021e |
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author | Gong, Jue Katz, Michael J. Kerton, Francesca M. |
author_facet | Gong, Jue Katz, Michael J. Kerton, Francesca M. |
author_sort | Gong, Jue |
collection | PubMed |
description | 5-Hydroxymethylfurfural (5-HMF) can be prepared by the catalytic dehydration of glucose or fructose using a range of homogeneous or heterogeneous catalysts. For our research, a selection of closely related Metal–Organic Frameworks (MOFs) were used as catalysts in the conversion of glucose to 5-HMF due to their chemical and thermal stability as well as the Lewis acidity of zirconium. Our initial study focused on the use of UiO-66–X (X = H, NH(2) and SO(3)H), optimization of the dehydration reaction conditions, and correlation of the catalytic activity with the MOF's properties, in particular, their surface area. The highest yield of 5-HMF (28%) could be obtained using UiO-66 under optimal reaction conditions in dimethylsulfoxide and this could be increased to 37% in the presence of water. In catalyst recycling tests, we found the efficiency of UiO-66 was maintained across five runs (23%, 19%, 21%, 20%, 22.5%). The post-catalysis MOF, UiO-66–humin, was characterized using a range of techniques including PXRD, FT-IR, (13)C Solid State NMR and N(2) gas adsorption. We continued to optimize the reaction using MOF 808 as the catalyst. Notably, MOF 808 afforded higher yields of 5-HMF under the same conditions compared with the three UiO-66–X compounds. We propose that this might be attributed to the larger pores of MOF 808 or the more accessible zirconium centres. |
format | Online Article Text |
id | pubmed-9085719 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90857192022-05-10 Catalytic conversion of glucose to 5-hydroxymethylfurfural using zirconium-containing metal–organic frameworks using microwave heating Gong, Jue Katz, Michael J. Kerton, Francesca M. RSC Adv Chemistry 5-Hydroxymethylfurfural (5-HMF) can be prepared by the catalytic dehydration of glucose or fructose using a range of homogeneous or heterogeneous catalysts. For our research, a selection of closely related Metal–Organic Frameworks (MOFs) were used as catalysts in the conversion of glucose to 5-HMF due to their chemical and thermal stability as well as the Lewis acidity of zirconium. Our initial study focused on the use of UiO-66–X (X = H, NH(2) and SO(3)H), optimization of the dehydration reaction conditions, and correlation of the catalytic activity with the MOF's properties, in particular, their surface area. The highest yield of 5-HMF (28%) could be obtained using UiO-66 under optimal reaction conditions in dimethylsulfoxide and this could be increased to 37% in the presence of water. In catalyst recycling tests, we found the efficiency of UiO-66 was maintained across five runs (23%, 19%, 21%, 20%, 22.5%). The post-catalysis MOF, UiO-66–humin, was characterized using a range of techniques including PXRD, FT-IR, (13)C Solid State NMR and N(2) gas adsorption. We continued to optimize the reaction using MOF 808 as the catalyst. Notably, MOF 808 afforded higher yields of 5-HMF under the same conditions compared with the three UiO-66–X compounds. We propose that this might be attributed to the larger pores of MOF 808 or the more accessible zirconium centres. The Royal Society of Chemistry 2018-09-10 /pmc/articles/PMC9085719/ /pubmed/35548202 http://dx.doi.org/10.1039/c8ra06021e Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Gong, Jue Katz, Michael J. Kerton, Francesca M. Catalytic conversion of glucose to 5-hydroxymethylfurfural using zirconium-containing metal–organic frameworks using microwave heating |
title | Catalytic conversion of glucose to 5-hydroxymethylfurfural using zirconium-containing metal–organic frameworks using microwave heating |
title_full | Catalytic conversion of glucose to 5-hydroxymethylfurfural using zirconium-containing metal–organic frameworks using microwave heating |
title_fullStr | Catalytic conversion of glucose to 5-hydroxymethylfurfural using zirconium-containing metal–organic frameworks using microwave heating |
title_full_unstemmed | Catalytic conversion of glucose to 5-hydroxymethylfurfural using zirconium-containing metal–organic frameworks using microwave heating |
title_short | Catalytic conversion of glucose to 5-hydroxymethylfurfural using zirconium-containing metal–organic frameworks using microwave heating |
title_sort | catalytic conversion of glucose to 5-hydroxymethylfurfural using zirconium-containing metal–organic frameworks using microwave heating |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9085719/ https://www.ncbi.nlm.nih.gov/pubmed/35548202 http://dx.doi.org/10.1039/c8ra06021e |
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