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Carbon-Supported Raney Nickel Catalyst for Acetone Hydrogenation with High Selectivity
Catalysts with high selectivity play key roles in green chemistry. In this work, a granular Raney Ni catalyst using carbon as support (Raney Ni/C) was developed by mixing phenolic resin with Ni-Al alloy, conducting carbonization at high temperature, and leaching with alkaline liquor. The as-prepared...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7070612/ https://www.ncbi.nlm.nih.gov/pubmed/32069793 http://dx.doi.org/10.3390/molecules25040803 |
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author | Lu, Shuliang Wu, Jiajia Peng, Hui Chen, Yong |
author_facet | Lu, Shuliang Wu, Jiajia Peng, Hui Chen, Yong |
author_sort | Lu, Shuliang |
collection | PubMed |
description | Catalysts with high selectivity play key roles in green chemistry. In this work, a granular Raney Ni catalyst using carbon as support (Raney Ni/C) was developed by mixing phenolic resin with Ni-Al alloy, conducting carbonization at high temperature, and leaching with alkaline liquor. The as-prepared Raney Ni/C catalyst is suitable for use in fix-bed reactors. Moreover, it shows high activity and selectivity for catalytic acetone hydrogenation. For instance, at the reaction temperature of 120 °C, the conversion of acetone can reach up to 99.9% and the main byproduct methyl isobutylcarbinol (MIBC) content can be diminished to 0.02 wt%. The Raney Ni/C may represent a new type of shaped Raney metal catalysts, which are important fix-bed catalysts in chemical industry. |
format | Online Article Text |
id | pubmed-7070612 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-70706122020-03-19 Carbon-Supported Raney Nickel Catalyst for Acetone Hydrogenation with High Selectivity Lu, Shuliang Wu, Jiajia Peng, Hui Chen, Yong Molecules Communication Catalysts with high selectivity play key roles in green chemistry. In this work, a granular Raney Ni catalyst using carbon as support (Raney Ni/C) was developed by mixing phenolic resin with Ni-Al alloy, conducting carbonization at high temperature, and leaching with alkaline liquor. The as-prepared Raney Ni/C catalyst is suitable for use in fix-bed reactors. Moreover, it shows high activity and selectivity for catalytic acetone hydrogenation. For instance, at the reaction temperature of 120 °C, the conversion of acetone can reach up to 99.9% and the main byproduct methyl isobutylcarbinol (MIBC) content can be diminished to 0.02 wt%. The Raney Ni/C may represent a new type of shaped Raney metal catalysts, which are important fix-bed catalysts in chemical industry. MDPI 2020-02-13 /pmc/articles/PMC7070612/ /pubmed/32069793 http://dx.doi.org/10.3390/molecules25040803 Text en © 2020 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 | Communication Lu, Shuliang Wu, Jiajia Peng, Hui Chen, Yong Carbon-Supported Raney Nickel Catalyst for Acetone Hydrogenation with High Selectivity |
title | Carbon-Supported Raney Nickel Catalyst for Acetone Hydrogenation with High Selectivity |
title_full | Carbon-Supported Raney Nickel Catalyst for Acetone Hydrogenation with High Selectivity |
title_fullStr | Carbon-Supported Raney Nickel Catalyst for Acetone Hydrogenation with High Selectivity |
title_full_unstemmed | Carbon-Supported Raney Nickel Catalyst for Acetone Hydrogenation with High Selectivity |
title_short | Carbon-Supported Raney Nickel Catalyst for Acetone Hydrogenation with High Selectivity |
title_sort | carbon-supported raney nickel catalyst for acetone hydrogenation with high selectivity |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7070612/ https://www.ncbi.nlm.nih.gov/pubmed/32069793 http://dx.doi.org/10.3390/molecules25040803 |
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