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Deactivation and Regeneration of Nitrogen Doped Carbon Catalyst for Acetylene Hydrochlorination

The poor stability of carbon materials doped with nitrogen limited their development in acetylene hydrochlorination. Therefore, investigating the deactivation reasons of carbon catalysts and researching regeneration methods became the research focus. Herein, carbon-nitrogen materials were synthesize...

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Detalles Bibliográficos
Autores principales: Lu, Fangjie, Wang, Qinqin, Zhu, Mingyuan, Dai, Bin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9919228/
https://www.ncbi.nlm.nih.gov/pubmed/36770621
http://dx.doi.org/10.3390/molecules28030956
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author Lu, Fangjie
Wang, Qinqin
Zhu, Mingyuan
Dai, Bin
author_facet Lu, Fangjie
Wang, Qinqin
Zhu, Mingyuan
Dai, Bin
author_sort Lu, Fangjie
collection PubMed
description The poor stability of carbon materials doped with nitrogen limited their development in acetylene hydrochlorination. Therefore, investigating the deactivation reasons of carbon catalysts and researching regeneration methods became the research focus. Herein, carbon-nitrogen materials were synthesized by one-step pyrolysis, which using biomass materials with high nitrogen content, the synthesized material was used in an acetylene hydrochlorination reaction. The acetylene conversion rate of D-GH-800 catalyst was up to 99%, but the catalytic activity decreased by 30% after 60 h reaction. Thermogravimetric analysis results showed that the coke content was 5.87%, resulting in catalyst deactivation. Temperature-programmed desorption verified that the deactivation was due to the strong adsorption and difficult desorption of acetylene by the D-GH-800 catalyst, resulting in the accumulation of acetylene on the catalyst surface to form carbon polymers and leading to the pore blockage phenomenon. Furthermore, based on the catalyst deactivation by carbon accumulation, we proposed a new idea of regeneration by ZnCl(2) activation to eliminate carbon deposition in the pores of the deactivated catalyst. As a result, the activity of D-GH-800 was recovered, and lifetime was also extended. Our strategy illustrated the mechanism of carbon deposition, and the recoverability of the catalyst has promising applications.
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spelling pubmed-99192282023-02-12 Deactivation and Regeneration of Nitrogen Doped Carbon Catalyst for Acetylene Hydrochlorination Lu, Fangjie Wang, Qinqin Zhu, Mingyuan Dai, Bin Molecules Article The poor stability of carbon materials doped with nitrogen limited their development in acetylene hydrochlorination. Therefore, investigating the deactivation reasons of carbon catalysts and researching regeneration methods became the research focus. Herein, carbon-nitrogen materials were synthesized by one-step pyrolysis, which using biomass materials with high nitrogen content, the synthesized material was used in an acetylene hydrochlorination reaction. The acetylene conversion rate of D-GH-800 catalyst was up to 99%, but the catalytic activity decreased by 30% after 60 h reaction. Thermogravimetric analysis results showed that the coke content was 5.87%, resulting in catalyst deactivation. Temperature-programmed desorption verified that the deactivation was due to the strong adsorption and difficult desorption of acetylene by the D-GH-800 catalyst, resulting in the accumulation of acetylene on the catalyst surface to form carbon polymers and leading to the pore blockage phenomenon. Furthermore, based on the catalyst deactivation by carbon accumulation, we proposed a new idea of regeneration by ZnCl(2) activation to eliminate carbon deposition in the pores of the deactivated catalyst. As a result, the activity of D-GH-800 was recovered, and lifetime was also extended. Our strategy illustrated the mechanism of carbon deposition, and the recoverability of the catalyst has promising applications. MDPI 2023-01-18 /pmc/articles/PMC9919228/ /pubmed/36770621 http://dx.doi.org/10.3390/molecules28030956 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Lu, Fangjie
Wang, Qinqin
Zhu, Mingyuan
Dai, Bin
Deactivation and Regeneration of Nitrogen Doped Carbon Catalyst for Acetylene Hydrochlorination
title Deactivation and Regeneration of Nitrogen Doped Carbon Catalyst for Acetylene Hydrochlorination
title_full Deactivation and Regeneration of Nitrogen Doped Carbon Catalyst for Acetylene Hydrochlorination
title_fullStr Deactivation and Regeneration of Nitrogen Doped Carbon Catalyst for Acetylene Hydrochlorination
title_full_unstemmed Deactivation and Regeneration of Nitrogen Doped Carbon Catalyst for Acetylene Hydrochlorination
title_short Deactivation and Regeneration of Nitrogen Doped Carbon Catalyst for Acetylene Hydrochlorination
title_sort deactivation and regeneration of nitrogen doped carbon catalyst for acetylene hydrochlorination
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9919228/
https://www.ncbi.nlm.nih.gov/pubmed/36770621
http://dx.doi.org/10.3390/molecules28030956
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