Cargando…
Facile Synthesis of Micro-Mesoporous Copper Phyllosilicate Supported on a Commercial Carrier and Its Application for Catalytic Hydrogenation of Nitro-Group in Trinitrobenzene
Development of novel Cu-based catalysts has become one of the frontiers in the catalytic production of platform chemicals and in environment protection. However, the known methods of their synthesis are too complicated and result in materials that cannot be used instantly as commercial catalysts. In...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9414592/ https://www.ncbi.nlm.nih.gov/pubmed/36014388 http://dx.doi.org/10.3390/molecules27165147 |
_version_ | 1784776026002292736 |
---|---|
author | Kirichenko, Olga Kapustin, Gennady Mishin, Igor Nissenbaum, Vera Shuvalova, Elena Redina, Elena Kustov, Leonid |
author_facet | Kirichenko, Olga Kapustin, Gennady Mishin, Igor Nissenbaum, Vera Shuvalova, Elena Redina, Elena Kustov, Leonid |
author_sort | Kirichenko, Olga |
collection | PubMed |
description | Development of novel Cu-based catalysts has become one of the frontiers in the catalytic production of platform chemicals and in environment protection. However, the known methods of their synthesis are too complicated and result in materials that cannot be used instantly as commercial catalysts. In the present work, a novel material has been synthesized by the facile method of deposition–precipitation using thermal hydrolysis of urea. The conditions for Cu phyllosilicate formation have been revealed (molar ratio urea:copper = 10, 92 °C, 8–11 h). The prepared Cu-based materials were studied by TG–DTA, SEM, TEM, XRD, N(2) adsorption and TPR-H(2) methods, and it was found that the material involves nanoparticles of micro-mesoporous copper phyllosilicate phase with a chrysocolla-like structure inside the pores of a commercial meso-macroporous silica carrier. The chrysocolla-like phase is first shown to be catalytically active in the selective reduction of the nitro-group in trinitrobenzene to an amino-group with molecular hydrogen. Complete conversion of trinitrobenzene with a high yield of amines has been achieved in short time under relatively mild conditions (170 °C, 1.3 MPa) of nitroarene hydrogenation over a copper catalyst. |
format | Online Article Text |
id | pubmed-9414592 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-94145922022-08-27 Facile Synthesis of Micro-Mesoporous Copper Phyllosilicate Supported on a Commercial Carrier and Its Application for Catalytic Hydrogenation of Nitro-Group in Trinitrobenzene Kirichenko, Olga Kapustin, Gennady Mishin, Igor Nissenbaum, Vera Shuvalova, Elena Redina, Elena Kustov, Leonid Molecules Article Development of novel Cu-based catalysts has become one of the frontiers in the catalytic production of platform chemicals and in environment protection. However, the known methods of their synthesis are too complicated and result in materials that cannot be used instantly as commercial catalysts. In the present work, a novel material has been synthesized by the facile method of deposition–precipitation using thermal hydrolysis of urea. The conditions for Cu phyllosilicate formation have been revealed (molar ratio urea:copper = 10, 92 °C, 8–11 h). The prepared Cu-based materials were studied by TG–DTA, SEM, TEM, XRD, N(2) adsorption and TPR-H(2) methods, and it was found that the material involves nanoparticles of micro-mesoporous copper phyllosilicate phase with a chrysocolla-like structure inside the pores of a commercial meso-macroporous silica carrier. The chrysocolla-like phase is first shown to be catalytically active in the selective reduction of the nitro-group in trinitrobenzene to an amino-group with molecular hydrogen. Complete conversion of trinitrobenzene with a high yield of amines has been achieved in short time under relatively mild conditions (170 °C, 1.3 MPa) of nitroarene hydrogenation over a copper catalyst. MDPI 2022-08-12 /pmc/articles/PMC9414592/ /pubmed/36014388 http://dx.doi.org/10.3390/molecules27165147 Text en © 2022 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 Kirichenko, Olga Kapustin, Gennady Mishin, Igor Nissenbaum, Vera Shuvalova, Elena Redina, Elena Kustov, Leonid Facile Synthesis of Micro-Mesoporous Copper Phyllosilicate Supported on a Commercial Carrier and Its Application for Catalytic Hydrogenation of Nitro-Group in Trinitrobenzene |
title | Facile Synthesis of Micro-Mesoporous Copper Phyllosilicate Supported on a Commercial Carrier and Its Application for Catalytic Hydrogenation of Nitro-Group in Trinitrobenzene |
title_full | Facile Synthesis of Micro-Mesoporous Copper Phyllosilicate Supported on a Commercial Carrier and Its Application for Catalytic Hydrogenation of Nitro-Group in Trinitrobenzene |
title_fullStr | Facile Synthesis of Micro-Mesoporous Copper Phyllosilicate Supported on a Commercial Carrier and Its Application for Catalytic Hydrogenation of Nitro-Group in Trinitrobenzene |
title_full_unstemmed | Facile Synthesis of Micro-Mesoporous Copper Phyllosilicate Supported on a Commercial Carrier and Its Application for Catalytic Hydrogenation of Nitro-Group in Trinitrobenzene |
title_short | Facile Synthesis of Micro-Mesoporous Copper Phyllosilicate Supported on a Commercial Carrier and Its Application for Catalytic Hydrogenation of Nitro-Group in Trinitrobenzene |
title_sort | facile synthesis of micro-mesoporous copper phyllosilicate supported on a commercial carrier and its application for catalytic hydrogenation of nitro-group in trinitrobenzene |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9414592/ https://www.ncbi.nlm.nih.gov/pubmed/36014388 http://dx.doi.org/10.3390/molecules27165147 |
work_keys_str_mv | AT kirichenkoolga facilesynthesisofmicromesoporouscopperphyllosilicatesupportedonacommercialcarrieranditsapplicationforcatalytichydrogenationofnitrogroupintrinitrobenzene AT kapustingennady facilesynthesisofmicromesoporouscopperphyllosilicatesupportedonacommercialcarrieranditsapplicationforcatalytichydrogenationofnitrogroupintrinitrobenzene AT mishinigor facilesynthesisofmicromesoporouscopperphyllosilicatesupportedonacommercialcarrieranditsapplicationforcatalytichydrogenationofnitrogroupintrinitrobenzene AT nissenbaumvera facilesynthesisofmicromesoporouscopperphyllosilicatesupportedonacommercialcarrieranditsapplicationforcatalytichydrogenationofnitrogroupintrinitrobenzene AT shuvalovaelena facilesynthesisofmicromesoporouscopperphyllosilicatesupportedonacommercialcarrieranditsapplicationforcatalytichydrogenationofnitrogroupintrinitrobenzene AT redinaelena facilesynthesisofmicromesoporouscopperphyllosilicatesupportedonacommercialcarrieranditsapplicationforcatalytichydrogenationofnitrogroupintrinitrobenzene AT kustovleonid facilesynthesisofmicromesoporouscopperphyllosilicatesupportedonacommercialcarrieranditsapplicationforcatalytichydrogenationofnitrogroupintrinitrobenzene |