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Supported Ni Catalyst for Liquid Phase Hydrogenation of Adiponitrile to 6-Aminocapronitrile and Hexamethyenediamine

Supported Ni catalysts prepared under different conditions, for liquid phase hydrogenation of adiponitrile (ADN) to 6-aminocapronitrile (ACN) and hexamethyenediamine (HMD), were investigated. The highly reactive imine intermediate can form condensation byproducts with primary amine products (ACN and...

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Autores principales: Wang, Chengqiang, Jia, Zekun, Zhen, Bin, Han, Minghan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6017426/
https://www.ncbi.nlm.nih.gov/pubmed/29300298
http://dx.doi.org/10.3390/molecules23010092
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author Wang, Chengqiang
Jia, Zekun
Zhen, Bin
Han, Minghan
author_facet Wang, Chengqiang
Jia, Zekun
Zhen, Bin
Han, Minghan
author_sort Wang, Chengqiang
collection PubMed
description Supported Ni catalysts prepared under different conditions, for liquid phase hydrogenation of adiponitrile (ADN) to 6-aminocapronitrile (ACN) and hexamethyenediamine (HMD), were investigated. The highly reactive imine intermediate can form condensation byproducts with primary amine products (ACN and HMD), which decreased the yield coefficient of primary amines. The catalysts support, condition of catalyst preparation and dosage of additive were studied to improve the yield. A highly dispersed Ni/SiO(2) catalyst prepared by the direct reduction of Ni(NO(3))(2)/SiO(2) suppressed the condensation reactions by promoting the hydrogenation of adsorbed imines, and it gave the improved hydrogenation activity of 0.63 mol·kg(cat)(−1)·min(−1) and primary amine selectivity of 94% when NaOH was added into the reactor.
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spelling pubmed-60174262018-11-13 Supported Ni Catalyst for Liquid Phase Hydrogenation of Adiponitrile to 6-Aminocapronitrile and Hexamethyenediamine Wang, Chengqiang Jia, Zekun Zhen, Bin Han, Minghan Molecules Article Supported Ni catalysts prepared under different conditions, for liquid phase hydrogenation of adiponitrile (ADN) to 6-aminocapronitrile (ACN) and hexamethyenediamine (HMD), were investigated. The highly reactive imine intermediate can form condensation byproducts with primary amine products (ACN and HMD), which decreased the yield coefficient of primary amines. The catalysts support, condition of catalyst preparation and dosage of additive were studied to improve the yield. A highly dispersed Ni/SiO(2) catalyst prepared by the direct reduction of Ni(NO(3))(2)/SiO(2) suppressed the condensation reactions by promoting the hydrogenation of adsorbed imines, and it gave the improved hydrogenation activity of 0.63 mol·kg(cat)(−1)·min(−1) and primary amine selectivity of 94% when NaOH was added into the reactor. MDPI 2018-01-04 /pmc/articles/PMC6017426/ /pubmed/29300298 http://dx.doi.org/10.3390/molecules23010092 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Wang, Chengqiang
Jia, Zekun
Zhen, Bin
Han, Minghan
Supported Ni Catalyst for Liquid Phase Hydrogenation of Adiponitrile to 6-Aminocapronitrile and Hexamethyenediamine
title Supported Ni Catalyst for Liquid Phase Hydrogenation of Adiponitrile to 6-Aminocapronitrile and Hexamethyenediamine
title_full Supported Ni Catalyst for Liquid Phase Hydrogenation of Adiponitrile to 6-Aminocapronitrile and Hexamethyenediamine
title_fullStr Supported Ni Catalyst for Liquid Phase Hydrogenation of Adiponitrile to 6-Aminocapronitrile and Hexamethyenediamine
title_full_unstemmed Supported Ni Catalyst for Liquid Phase Hydrogenation of Adiponitrile to 6-Aminocapronitrile and Hexamethyenediamine
title_short Supported Ni Catalyst for Liquid Phase Hydrogenation of Adiponitrile to 6-Aminocapronitrile and Hexamethyenediamine
title_sort supported ni catalyst for liquid phase hydrogenation of adiponitrile to 6-aminocapronitrile and hexamethyenediamine
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6017426/
https://www.ncbi.nlm.nih.gov/pubmed/29300298
http://dx.doi.org/10.3390/molecules23010092
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