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Hydroxylation of benzene to phenol over heteropoly acid H(5)PMo(10)V(2)O(40) supported on amine-functionalized MCM-41
Supported catalysts with Keggin type heteropoly acids (H(5)PMo(10)V(2)O(40)) loaded onto amine-functionalized MCM-41 for the catalytic hydroxylation of benzene to phenol with H(2)O(2) were prepared by a wet impregnation method. The effects of the preparation conditions on the properties and activity...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Royal Society of Chemistry
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9037690/ https://www.ncbi.nlm.nih.gov/pubmed/35480001 http://dx.doi.org/10.1039/d1ra04269f |
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author | Li, Yanjun Li, Shichao Kong, Yan |
author_facet | Li, Yanjun Li, Shichao Kong, Yan |
author_sort | Li, Yanjun |
collection | PubMed |
description | Supported catalysts with Keggin type heteropoly acids (H(5)PMo(10)V(2)O(40)) loaded onto amine-functionalized MCM-41 for the catalytic hydroxylation of benzene to phenol with H(2)O(2) were prepared by a wet impregnation method. The effects of the preparation conditions on the properties and activity of the supported catalysts were fully investigated. The results showed that the catalyst retained the mesoporous structure of MCM-41 and H(5)PMo(10)V(2)O(40) was dispersed uniformly on the surface of the amine-functionalized MCM-41. Meanwhile, the reusability and catalytic performance of the catalyst were affected by two key factors, i.e., the interaction between the heteropoly acid and the surface of MCM-41, and the hydrophobicity of the catalyst since they decide the leaching of H(5)PMo(10)V(2)O(40) and the adsorption of benzene. The catalyst with H(5)PMo(10)V(2)O(40) loaded onto amine-functionalized MCM-41, which was prepared using ethanol as the solvent, exhibited the highest phenol yield (20.4%), a turnover frequency value of 20.3 h(−1) and good reusability. We believe this work offers an effective and facile strategy for the preparation of a new catalyst for hydroxylation of benzene to phenol. |
format | Online Article Text |
id | pubmed-9037690 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90376902022-04-26 Hydroxylation of benzene to phenol over heteropoly acid H(5)PMo(10)V(2)O(40) supported on amine-functionalized MCM-41 Li, Yanjun Li, Shichao Kong, Yan RSC Adv Chemistry Supported catalysts with Keggin type heteropoly acids (H(5)PMo(10)V(2)O(40)) loaded onto amine-functionalized MCM-41 for the catalytic hydroxylation of benzene to phenol with H(2)O(2) were prepared by a wet impregnation method. The effects of the preparation conditions on the properties and activity of the supported catalysts were fully investigated. The results showed that the catalyst retained the mesoporous structure of MCM-41 and H(5)PMo(10)V(2)O(40) was dispersed uniformly on the surface of the amine-functionalized MCM-41. Meanwhile, the reusability and catalytic performance of the catalyst were affected by two key factors, i.e., the interaction between the heteropoly acid and the surface of MCM-41, and the hydrophobicity of the catalyst since they decide the leaching of H(5)PMo(10)V(2)O(40) and the adsorption of benzene. The catalyst with H(5)PMo(10)V(2)O(40) loaded onto amine-functionalized MCM-41, which was prepared using ethanol as the solvent, exhibited the highest phenol yield (20.4%), a turnover frequency value of 20.3 h(−1) and good reusability. We believe this work offers an effective and facile strategy for the preparation of a new catalyst for hydroxylation of benzene to phenol. The Royal Society of Chemistry 2021-08-03 /pmc/articles/PMC9037690/ /pubmed/35480001 http://dx.doi.org/10.1039/d1ra04269f Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Li, Yanjun Li, Shichao Kong, Yan Hydroxylation of benzene to phenol over heteropoly acid H(5)PMo(10)V(2)O(40) supported on amine-functionalized MCM-41 |
title | Hydroxylation of benzene to phenol over heteropoly acid H(5)PMo(10)V(2)O(40) supported on amine-functionalized MCM-41 |
title_full | Hydroxylation of benzene to phenol over heteropoly acid H(5)PMo(10)V(2)O(40) supported on amine-functionalized MCM-41 |
title_fullStr | Hydroxylation of benzene to phenol over heteropoly acid H(5)PMo(10)V(2)O(40) supported on amine-functionalized MCM-41 |
title_full_unstemmed | Hydroxylation of benzene to phenol over heteropoly acid H(5)PMo(10)V(2)O(40) supported on amine-functionalized MCM-41 |
title_short | Hydroxylation of benzene to phenol over heteropoly acid H(5)PMo(10)V(2)O(40) supported on amine-functionalized MCM-41 |
title_sort | hydroxylation of benzene to phenol over heteropoly acid h(5)pmo(10)v(2)o(40) supported on amine-functionalized mcm-41 |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9037690/ https://www.ncbi.nlm.nih.gov/pubmed/35480001 http://dx.doi.org/10.1039/d1ra04269f |
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