Organodiphosphonate Metal‐Organic Frameworks Derived Ni‐P@C Catalyst for Hydrogenation of Furfural

Tetraethyl p‐xylenediphosphate is used as the organic ligand to prepare the Ni−P‐MOFs material belonging to the category of organic phosphoric acids, through pyrolysis and in‐situ reduction reaction of Ni−P‐MOFs material during the high‐temperature carbonization process, Ni−P@C catalyst with graphit...

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Veröffentlicht in:ChemistrySelect (Weinheim) 2020-02, Vol.5 (7), p.2271-2278
Hauptverfasser: Li, Feng, Jiang, Shanshan, Zhu, Tianhan, Wang, Yue, Huang, Tao, Li, Cuiqin
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Jiang, Shanshan
Zhu, Tianhan
Wang, Yue
Huang, Tao
Li, Cuiqin
description Tetraethyl p‐xylenediphosphate is used as the organic ligand to prepare the Ni−P‐MOFs material belonging to the category of organic phosphoric acids, through pyrolysis and in‐situ reduction reaction of Ni−P‐MOFs material during the high‐temperature carbonization process, Ni−P@C catalyst with graphitized carbon‐covering Ni2P particles is prepared. Compared with Ni−P catalyst prepared through coprecipitation method, Ni−P@C catalyst prepared with Ni−P‐MOFs material can obviously decrease the formation temperature of Ni2P active phase and retain the schistose morphology of the Ni−P‐MOFs material, which is of high specific area, and meanwhile effectively suppresses the agglomeration of Ni2P particles. It is indicated by research on furfural hydrogenation performance that, Ni−P@C catalyst presents a high activity and stability in furfural hydrogenation. Products of furfural hydrogenation catalyzed by Ni−P@C catalyst mainly contain furfuryl alcohol, 2‐methylfuran and 2‐methyltetra hydrofuran, and the reaction temperature and reaction time have great influence on the distribution of products. The carbon‐covering structure of Ni−P@C catalyst can effectively protect the active components of Ni2P, thus presenting a high stability and good reusability. Ni−P‐MOFs material was prepared using tetraethyl p‐xylenediphosphate as the organic ligand. Ni−P@C catalyst with graphitized carbon‐covering Ni2P particles was prepared by pyrolysis and in‐situ reduction method using Ni−P−MOFs material as the precursor. Ni−P@C catalyst presented a high activity in furfural hydrogenation, and the selectivity of reaction products greatly dependent on the reaction temperature and reaction time.
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Compared with Ni−P catalyst prepared through coprecipitation method, Ni−P@C catalyst prepared with Ni−P‐MOFs material can obviously decrease the formation temperature of Ni2P active phase and retain the schistose morphology of the Ni−P‐MOFs material, which is of high specific area, and meanwhile effectively suppresses the agglomeration of Ni2P particles. It is indicated by research on furfural hydrogenation performance that, Ni−P@C catalyst presents a high activity and stability in furfural hydrogenation. Products of furfural hydrogenation catalyzed by Ni−P@C catalyst mainly contain furfuryl alcohol, 2‐methylfuran and 2‐methyltetra hydrofuran, and the reaction temperature and reaction time have great influence on the distribution of products. The carbon‐covering structure of Ni−P@C catalyst can effectively protect the active components of Ni2P, thus presenting a high stability and good reusability. Ni−P‐MOFs material was prepared using tetraethyl p‐xylenediphosphate as the organic ligand. Ni−P@C catalyst with graphitized carbon‐covering Ni2P particles was prepared by pyrolysis and in‐situ reduction method using Ni−P−MOFs material as the precursor. Ni−P@C catalyst presented a high activity in furfural hydrogenation, and the selectivity of reaction products greatly dependent on the reaction temperature and reaction time.</description><identifier>ISSN: 2365-6549</identifier><identifier>EISSN: 2365-6549</identifier><identifier>DOI: 10.1002/slct.201902827</identifier><language>eng</language><subject>Furfural ; hydrogenation ; metal-organic frameworks ; nickel phosphide</subject><ispartof>ChemistrySelect (Weinheim), 2020-02, Vol.5 (7), p.2271-2278</ispartof><rights>2020 Wiley‐VCH Verlag GmbH &amp; Co. 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Compared with Ni−P catalyst prepared through coprecipitation method, Ni−P@C catalyst prepared with Ni−P‐MOFs material can obviously decrease the formation temperature of Ni2P active phase and retain the schistose morphology of the Ni−P‐MOFs material, which is of high specific area, and meanwhile effectively suppresses the agglomeration of Ni2P particles. It is indicated by research on furfural hydrogenation performance that, Ni−P@C catalyst presents a high activity and stability in furfural hydrogenation. Products of furfural hydrogenation catalyzed by Ni−P@C catalyst mainly contain furfuryl alcohol, 2‐methylfuran and 2‐methyltetra hydrofuran, and the reaction temperature and reaction time have great influence on the distribution of products. The carbon‐covering structure of Ni−P@C catalyst can effectively protect the active components of Ni2P, thus presenting a high stability and good reusability. 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Compared with Ni−P catalyst prepared through coprecipitation method, Ni−P@C catalyst prepared with Ni−P‐MOFs material can obviously decrease the formation temperature of Ni2P active phase and retain the schistose morphology of the Ni−P‐MOFs material, which is of high specific area, and meanwhile effectively suppresses the agglomeration of Ni2P particles. It is indicated by research on furfural hydrogenation performance that, Ni−P@C catalyst presents a high activity and stability in furfural hydrogenation. Products of furfural hydrogenation catalyzed by Ni−P@C catalyst mainly contain furfuryl alcohol, 2‐methylfuran and 2‐methyltetra hydrofuran, and the reaction temperature and reaction time have great influence on the distribution of products. The carbon‐covering structure of Ni−P@C catalyst can effectively protect the active components of Ni2P, thus presenting a high stability and good reusability. Ni−P‐MOFs material was prepared using tetraethyl p‐xylenediphosphate as the organic ligand. Ni−P@C catalyst with graphitized carbon‐covering Ni2P particles was prepared by pyrolysis and in‐situ reduction method using Ni−P−MOFs material as the precursor. Ni−P@C catalyst presented a high activity in furfural hydrogenation, and the selectivity of reaction products greatly dependent on the reaction temperature and reaction time.</abstract><doi>10.1002/slct.201902827</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-4278-0215</orcidid></addata></record>
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subjects Furfural
hydrogenation
metal-organic frameworks
nickel phosphide
title Organodiphosphonate Metal‐Organic Frameworks Derived Ni‐P@C Catalyst for Hydrogenation of Furfural
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