A switchable hydrogenation chemoselectivity of biomass platform compounds based on solvent regulation

被引:17
作者
Zhang, Yuanjing [1 ]
Wang, Si [1 ]
Yang, Yusen [1 ,2 ]
Wang, Lei [1 ,2 ]
Xu, Enze [1 ]
Hou, Quandong [1 ]
Zhao, Shiquan [1 ]
Liu, Tianyong [1 ]
Hong, Song [1 ]
Zheng, Lirong [3 ]
Li, Feng [1 ]
Zhang, Xin [1 ,2 ]
Wei, Min [1 ,2 ]
机构
[1] Beijing Univ Chem Technol, Beijing Adv Innovat Ctr Soft Matter Sci & Engn, State Key Lab Chem Resource Engn, Beijing 100029, Peoples R China
[2] Quzhou Inst Innovat Resource Chem Engn, Quzhou 324000, Peoples R China
[3] Chinese Acad Sci, Inst High Energy Phys, Beijing 100049, Peoples R China
来源
APPLIED CATALYSIS B-ENVIRONMENT AND ENERGY | 2024年 / 346卷
基金
中国国家自然科学基金;
关键词
Solvent effect; Selective hydrogenation; Fully exposed cluster catalyst; Adsorption configuration; Structure -selectivity relationship; ZEOLITE CRYSTALS; SELECTIVITY; CONVERSION; REDUCTION;
D O I
10.1016/j.apcatb.2024.123719
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Selective catalytic conversion of biomass-derived compounds to fuels and fine chemicals serves as a renewable energy pathway for the partial substitution of fossil resources, in which reaction pathway and selectivity control are key issues. Herein, we report a fully exposed Pt clusters immobilized on CoAl mixed metal oxides catalyst (denoted as Ptn/CoAl-MMOs), which exhibits prominent catalytic performance towards liquid phase hydrogenation reaction of furfural (FAL). Noteworthily, the hydrogenation chemoselectivity can be switched among four products via using four different solvents: tetrahydrofurfuryl alcohol (THFA; yield: 91.4%), furfuryl alcohol (FA; yield: 97.7%), 2-methylfuran (2-MF; yield: 92.1%) and furan (FU; yield: 90.8%) are obtained in ethanol, dioxane, isopropanol and n-hexane solvent, respectively. Experimental studies (in situ FT-IR and TPSR-Mass) combined with theoretical calculations (DFT) reveal that solvent molecules exert an essential influence on the adsorption configuration of FAL via changing the solvent-catalyst and/or substrate-catalyst interaction, which ultimately determines the hydrogenation pathway, key intermediate and final product. This work demonstrates a facile solvent-dependent product-switching strategy within one catalytic system, which opens up potential opportunities for tailoring hydrogenation selectivity in liquid-solid catalytic reactions towards biomass upgrading.
引用
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页数:10
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