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Ni-based MOFs catalytic oxidative cleavage of lignin models and lignosulfonate under oxygen atmosphere  ( SCI-EXPANDED收录 EI收录)   被引量:9

文献类型:期刊文献

英文题名:Ni-based MOFs catalytic oxidative cleavage of lignin models and lignosulfonate under oxygen atmosphere

作者:Zhou, Minghao[1] Tang, Chengjun[1] Xia, Haihong[2] Li, Jing[2] Liu, Junli[2] Jiang, Jianchun[2] Zhao, Jun[3] Yang, Xiaohui[2] Chen, Changzhou[2,3]

第一作者:Zhou, Minghao

通信作者:Zhou, MH[1];Yang, XH[1];Chen, CZ[1]

机构:[1]Yangzhou Univ, Sch Chem & Chem Engn, Yangzhou 225002, Jiangsu, Peoples R China;[2]Chinese Acad Forestry, Inst Chem Ind Forest Prod, Key Lab Biomass Energy & Mat, Nanjing 210042, Jiangsu, Peoples R China;[3]Hong Kong Baptist Univ, Inst Bioresource & Agr, Dept Biol, Kowloon Tong, Hong Kong 999077, Peoples R China

年份:2022

卷号:320

外文期刊名:FUEL

收录:;EI(收录号:20220063026);Scopus(收录号:2-s2.0-85127318844);WOS:【SCI-EXPANDED(收录号:WOS:000806820700004)】;

基金:Acknowledgements Authors are grateful for the financial support from the National Key Research and Development Program of China (No. 2021YFC2101604) and National Natural Science Foundation of China (31700645) .

语种:英文

外文关键词:Lignin; Oxidative depolymerization; Oxygen; Phenolics; Fuels

摘要:A strategy has now been created to immobilize non-noble metal particles on supports using metal-organic frameworks (MOFs) as precursors. Ni/C-X and other metal-based catalysts were synthesized using trimesic acid as ligand to transform lignin dimer and lignin to obtain high value-added fuels or chemicals (benzoic acid and phenol). Then, a mild Ni-based catalytic oxidation system under O-2 atmosphere was established. The introduction of Ni enhanced the strong acid sites of the spherical MOF catalyst, and the synergistic effect between the Ni and carbon support greatly improved the catalytic activity. Under optimal catalytic conditions, Ni/C-10 catalyst could break the beta-O-4 bond in lignin dimer under 160 degrees C for the production of benzoic acid and phenols. In addition, Ni/C-10 catalyst also showed excellent desulfurization ability in the oxidation depolymerization of lignosulfonate.

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