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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...

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Autores principales: Cao, Junya, Han, Fenggang, Wang, Liguo, Huang, Xiaoyu, Cao, Yan, He, Peng, Yang, Huanhuan, Chen, Jiaqiang, Li, Huiquan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
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.
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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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