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A Mutual Self-Assembly of Lignin and Metal-Organic Frameworks for the Catalytic Hydrodeoxygenation of Guaiacol to Cyclohexanol  ( EI收录)  

文献类型:期刊文献

英文题名:A Mutual Self-Assembly of Lignin and Metal-Organic Frameworks for the Catalytic Hydrodeoxygenation of Guaiacol to Cyclohexanol

作者:Ge, Fei[1] Xia, Haihong[2] Li, Jing[2] Xue, Yaqi[1] Su, Jiantao[1] Yang, Xiaohui[2] Jiang, Jianchun[2] Zhou, Minghao[1]

第一作者:Ge, Fei

机构:[1] School of Chemistry and Chemical Engineering, Yangzhou University, Yangzhou, 225002, China; [2] Institute of Chemical Industry of Forest Products, Chinese Academy of Forestry, Nanjing, 210042, China

年份:2023

外文期刊名:SSRN

收录:EI(收录号:20230113139)

语种:英文

外文关键词:Alcohols - Ammonia - Organometallics - Particle size - Petroleum transportation - Self assembly

摘要:Catalytic upgrading lignin-derived bio-oil with high oxygen content to directly usable transport fuel through hydrodeoxygenation (HDO) is highly desirable, but still remains a challenge. In this work, a series of Co-based catalysts were synthetized using metal-organic frameworks (MOFs) as a structure-directing agent and lignin as a renewable carbon precursor via a simple hydrothermal method. Among these catalysts, Co/C-EL-0.5-500 showed the best catalytic hydrodeoxygenation activity, affording 100% guaiacol conversion with 90% cyclohexanol yield under the conditions of 240 , 0 MPa N2 and 4 h. According to the characterization results of XRD, SEM, TEM, BET, ICP, NH3-TPD and XPS, the excellent performance of Co/C-EL-0.5-500 was attributed to large specific surface area, small Co particle size, and optimal acidity. The possible reaction pathway was proposed based on the products distribution. In addition, isopropanol was used as H-donor instead of extra hydrogen, and we hope that it could provide a novel strategy for bio-oil upgrading. ? 2023, The Authors. All rights reserved.

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