Water-favored reaction mechanism for selective catalytic conversion of 2-methylfuran to 1,4-pentanediol

被引:13
作者
Wu, Min [1 ]
Wang, Ting [2 ]
Li, Wenhui [1 ]
Zhang, Qin [1 ]
Zhang, Bin [1 ]
Chen, Kaiqin [1 ]
Peng, Siyuan [1 ]
Li, Guojia [1 ]
Huang, Jinning [1 ]
Wang, Qiang [1 ]
Wang, Chuan [1 ]
机构
[1] Nanjing Tech Univ, Sch Chem & Mol Engn, Nanjing 211816, Peoples R China
[2] Xiamen Univ, Coll Environm & Ecol, Xiamen 361102, Peoples R China
关键词
2-Methylfuran; Ring; -opening; Water; 4-Pentanediol; Bimetallic PtNi; PHASE HYDROGENATION; GAMMA-VALEROLACTONE; ALLOY NANOPARTICLES; CARBON NANOTUBES; HYDROGENOLYSIS; 1,2-PENTANEDIOL; SURFACES; GLUCOSE; ACID; NI;
D O I
10.1016/j.cej.2023.141944
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Water, as a cheap and easily available green solvent, is one of the most promising media in biomass conversion. Here, the water-favored one-pot conversion of 2-methylfuran (2-MF) to 1,4-pentanediol (1,4-PeD) under mild conditions was reported over a bimetallic PtNi catalyst supported on multi-walled carbon nanotubes (MWNT). In conjunction with theoretical calculations, we reveal that water significantly promote the furan ring ring-opening and the 1,4-PeD production. The Pt5Ni/MWNT catalyst affords a markedly improved catalytic activity (TOF of producing 93 1,4-PeD per site per hour) and yield (similar to 69%) to 1,4-PeD in the water-involved solvents compared to the water-free solvents. (H2O)-O-18 isotopic tracing experiments and kinetic studies directly validate water participated in the selective hydrogenation with hydrolysis process by providing a source of hydroxyl groups and lower the activation energy barrier. Such fundamental understanding of the intrinsic role of water as solvent opens a green and efficient door to promote the selective transformation of furanic platform compounds into valuable chemicals.
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页数:11
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