Cobalt Nanoparticles Embedded in N‐Doped Porous Carbon Derived from Bimetallic Zeolitic Imidazolate Frameworks for One‐Pot Selective Oxidative Depolymerization of Lignin

Cobalt nanoparticles embedded in N‐doped porous carbon (Co@CN) were prepared by the pyrolysis of bimetallic zeolitic imidazolate frameworks (BMZIFs) based on ZIF‐8 and ZIF‐67. The catalyst shows excellent catalytic efficiency in one‐pot selective oxidative cleavage of different linkages like β‐O‐4,...

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Published inChemCatChem Vol. 11; no. 4; pp. 1264 - 1271
Main Authors Sun, Kangkang, Chen, Shujie, Zhang, Jiawei, Lu, Guo‐Ping, Cai, Chun
Format Journal Article
LanguageEnglish
Published Weinheim Wiley Subscription Services, Inc 20.02.2019
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Abstract Cobalt nanoparticles embedded in N‐doped porous carbon (Co@CN) were prepared by the pyrolysis of bimetallic zeolitic imidazolate frameworks (BMZIFs) based on ZIF‐8 and ZIF‐67. The catalyst shows excellent catalytic efficiency in one‐pot selective oxidative cleavage of different linkages like β‐O‐4, a‐O‐4 and β‐1 in organosolv lignin and lignin model compounds in the presence of oxygen (ambient pressure) under mild conditions (383 K). Compared with traditional supported catalyst, the catalyst gives a highly hollow structure, which favored the adsorption of substrates and oxygen. The uniform cobalt nanoparticles surrounded by N‐doped graphitic structures and the strong electron transfer from graphitic nitrogen to Co NPs make it hard to be oxidized prior to use and higher catalytic reactivity. Moreover, the catalyst can be easily recovered by magnetic force after the reaction, and reused after reduction for five times without an obvious change in yields. Selective oxidative dissociation of lignin: One‐pot Co@CN catalyzed selective oxidative dissociation of lignin and lignin model compounds with different linkages like β‐O‐4, α‐O‐4 and β‐1 under mild conditions without the assistance of any acid, base, ligand or noble metal has been reported.
AbstractList Cobalt nanoparticles embedded in N‐doped porous carbon (Co@CN) were prepared by the pyrolysis of bimetallic zeolitic imidazolate frameworks (BMZIFs) based on ZIF‐8 and ZIF‐67. The catalyst shows excellent catalytic efficiency in one‐pot selective oxidative cleavage of different linkages like β‐O‐4, a‐O‐4 and β‐1 in organosolv lignin and lignin model compounds in the presence of oxygen (ambient pressure) under mild conditions (383 K). Compared with traditional supported catalyst, the catalyst gives a highly hollow structure, which favored the adsorption of substrates and oxygen. The uniform cobalt nanoparticles surrounded by N‐doped graphitic structures and the strong electron transfer from graphitic nitrogen to Co NPs make it hard to be oxidized prior to use and higher catalytic reactivity. Moreover, the catalyst can be easily recovered by magnetic force after the reaction, and reused after reduction for five times without an obvious change in yields. Selective oxidative dissociation of lignin: One‐pot Co@CN catalyzed selective oxidative dissociation of lignin and lignin model compounds with different linkages like β‐O‐4, α‐O‐4 and β‐1 under mild conditions without the assistance of any acid, base, ligand or noble metal has been reported.
Cobalt nanoparticles embedded in N ‐doped porous carbon (Co@CN) were prepared by the pyrolysis of bimetallic zeolitic imidazolate frameworks (BMZIFs) based on ZIF‐8 and ZIF‐67. The catalyst shows excellent catalytic efficiency in one‐pot selective oxidative cleavage of different linkages like β ‐O‐4, a ‐O‐4 and β ‐1 in organosolv lignin and lignin model compounds in the presence of oxygen (ambient pressure) under mild conditions (383 K). Compared with traditional supported catalyst, the catalyst gives a highly hollow structure, which favored the adsorption of substrates and oxygen. The uniform cobalt nanoparticles surrounded by N ‐doped graphitic structures and the strong electron transfer from graphitic nitrogen to Co NPs make it hard to be oxidized prior to use and higher catalytic reactivity. Moreover, the catalyst can be easily recovered by magnetic force after the reaction, and reused after reduction for five times without an obvious change in yields.
Cobalt nanoparticles embedded in N‐doped porous carbon (Co@CN) were prepared by the pyrolysis of bimetallic zeolitic imidazolate frameworks (BMZIFs) based on ZIF‐8 and ZIF‐67. The catalyst shows excellent catalytic efficiency in one‐pot selective oxidative cleavage of different linkages like β‐O‐4, a‐O‐4 and β‐1 in organosolv lignin and lignin model compounds in the presence of oxygen (ambient pressure) under mild conditions (383 K). Compared with traditional supported catalyst, the catalyst gives a highly hollow structure, which favored the adsorption of substrates and oxygen. The uniform cobalt nanoparticles surrounded by N‐doped graphitic structures and the strong electron transfer from graphitic nitrogen to Co NPs make it hard to be oxidized prior to use and higher catalytic reactivity. Moreover, the catalyst can be easily recovered by magnetic force after the reaction, and reused after reduction for five times without an obvious change in yields.
Author Lu, Guo‐Ping
Zhang, Jiawei
Sun, Kangkang
Cai, Chun
Chen, Shujie
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Snippet Cobalt nanoparticles embedded in N‐doped porous carbon (Co@CN) were prepared by the pyrolysis of bimetallic zeolitic imidazolate frameworks (BMZIFs) based on...
Cobalt nanoparticles embedded in N ‐doped porous carbon (Co@CN) were prepared by the pyrolysis of bimetallic zeolitic imidazolate frameworks (BMZIFs) based on...
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SubjectTerms Bimetallic zeolitic imidazolate frameworks
Bimetals
Carbon
Catalysis
Catalysts
Cobalt
Cobalt nanoparticles
Depolymerization
Electron transfer
Heterogeneous catalysis
Lignin
Magnetic fields
Metal-organic frameworks
Nanoparticles
Nitrogen
Oxidation depolymerization
Pressure
Pyrolysis
Substrates
Title Cobalt Nanoparticles Embedded in N‐Doped Porous Carbon Derived from Bimetallic Zeolitic Imidazolate Frameworks for One‐Pot Selective Oxidative Depolymerization of Lignin
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fcctc.201801752
https://www.proquest.com/docview/2183776566
Volume 11
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