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Ru/g-C(3)N(4) as an efficient catalyst for selective hydrogenation of aromatic diamines to alicyclic diamines
A series of Ru/g-C(3)N(4) materials with highly dispersed Ru were firstly prepared by an ultrasonic impregnation method using carbon nitride as a support. The catalysts were characterized by various techniques including BET and elemental analysis, ICP-AES, XPS, XRD, CO(2)-TPD and TEM. The results de...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9052785/ https://www.ncbi.nlm.nih.gov/pubmed/35498848 http://dx.doi.org/10.1039/d0ra00836b |
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author | Cao, Junya Han, Fenggang Wang, Liguo Huang, Xiaoyu Cao, Yan He, Peng Yang, Huanhuan Chen, Jiaqiang Li, Huiquan |
author_facet | Cao, Junya Han, Fenggang Wang, Liguo Huang, Xiaoyu Cao, Yan He, Peng Yang, Huanhuan Chen, Jiaqiang Li, Huiquan |
author_sort | Cao, Junya |
collection | PubMed |
description | A series of Ru/g-C(3)N(4) materials with highly dispersed Ru were firstly prepared by an ultrasonic impregnation method using carbon nitride as a support. The catalysts were characterized by various techniques including BET and elemental analysis, ICP-AES, XPS, XRD, CO(2)-TPD and TEM. The results demonstrated that Ru/g-C(3)N(4) materials with a mesoporous structure and highly dispersed Ru were successfully prepared. The chemo-selective hydrogenation of p-phenylenediamine (PPDA) to 1,4-cyclohexanediamine (CHDA) over Ru/g-C(3)N(4) as a model reaction was investigated in detail. PPDA conversion of 100% with a CHDA selectivity of more than 86% could be achieved under mild conditions. It can be inferred that the carbon nitride support possessed abundant basic sites and the Ru/g-C(3)N(4)-T catalysts provided suitable basicity for the aromatic ring hydrogenation. Compared to the N-free Ru/C catalyst, the involvement of nitrogen species in Ru/g-C(3)N(4) remarkably improved the catalytic performance. In addition, the recyclability of the catalyst demonstrated that the aggregation of Ru nanoparticles was responsible for the decrease of the catalytic activity. Furthermore, this strategy also could be expanded to the selective hydrogenation of other aromatic diamines to alicyclic diamines. |
format | Online Article Text |
id | pubmed-9052785 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90527852022-04-29 Ru/g-C(3)N(4) as an efficient catalyst for selective hydrogenation of aromatic diamines to alicyclic diamines Cao, Junya Han, Fenggang Wang, Liguo Huang, Xiaoyu Cao, Yan He, Peng Yang, Huanhuan Chen, Jiaqiang Li, Huiquan RSC Adv Chemistry A series of Ru/g-C(3)N(4) materials with highly dispersed Ru were firstly prepared by an ultrasonic impregnation method using carbon nitride as a support. The catalysts were characterized by various techniques including BET and elemental analysis, ICP-AES, XPS, XRD, CO(2)-TPD and TEM. The results demonstrated that Ru/g-C(3)N(4) materials with a mesoporous structure and highly dispersed Ru were successfully prepared. The chemo-selective hydrogenation of p-phenylenediamine (PPDA) to 1,4-cyclohexanediamine (CHDA) over Ru/g-C(3)N(4) as a model reaction was investigated in detail. PPDA conversion of 100% with a CHDA selectivity of more than 86% could be achieved under mild conditions. It can be inferred that the carbon nitride support possessed abundant basic sites and the Ru/g-C(3)N(4)-T catalysts provided suitable basicity for the aromatic ring hydrogenation. Compared to the N-free Ru/C catalyst, the involvement of nitrogen species in Ru/g-C(3)N(4) remarkably improved the catalytic performance. In addition, the recyclability of the catalyst demonstrated that the aggregation of Ru nanoparticles was responsible for the decrease of the catalytic activity. Furthermore, this strategy also could be expanded to the selective hydrogenation of other aromatic diamines to alicyclic diamines. The Royal Society of Chemistry 2020-04-25 /pmc/articles/PMC9052785/ /pubmed/35498848 http://dx.doi.org/10.1039/d0ra00836b Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Cao, Junya Han, Fenggang Wang, Liguo Huang, Xiaoyu Cao, Yan He, Peng Yang, Huanhuan Chen, Jiaqiang Li, Huiquan Ru/g-C(3)N(4) as an efficient catalyst for selective hydrogenation of aromatic diamines to alicyclic diamines |
title | Ru/g-C(3)N(4) as an efficient catalyst for selective hydrogenation of aromatic diamines to alicyclic diamines |
title_full | Ru/g-C(3)N(4) as an efficient catalyst for selective hydrogenation of aromatic diamines to alicyclic diamines |
title_fullStr | Ru/g-C(3)N(4) as an efficient catalyst for selective hydrogenation of aromatic diamines to alicyclic diamines |
title_full_unstemmed | Ru/g-C(3)N(4) as an efficient catalyst for selective hydrogenation of aromatic diamines to alicyclic diamines |
title_short | Ru/g-C(3)N(4) as an efficient catalyst for selective hydrogenation of aromatic diamines to alicyclic diamines |
title_sort | ru/g-c(3)n(4) as an efficient catalyst for selective hydrogenation of aromatic diamines to alicyclic diamines |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9052785/ https://www.ncbi.nlm.nih.gov/pubmed/35498848 http://dx.doi.org/10.1039/d0ra00836b |
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