Selective hydrogenolysis of 5-hydroxymethylfurfural to 2,5-dimethylfuran with ethanol as a hydrogen donor over β-Mo2C embedded in carbon microspheres

被引:14
|
作者
Cao, Ningning [1 ]
Chen, Yong [1 ]
Lu, Kaiyun [1 ]
Wu, Chengming [1 ]
Abudila, Buzaynafu [1 ]
Li, Jifan [1 ]
Liu, Chun-Ling [1 ]
Dong, Wen-Sheng [1 ]
机构
[1] Shaanxi Normal Univ, Sch Chem & Chem Engn, Key Lab Appl Surface & Colloid Chem SNNU, MOE, Xian 710062, Shaanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
CATALYTIC TRANSFER HYDROGENATION/HYDROGENOLYSIS; LIQUID FUEL 2,5-DIMETHYLFURAN; IN-SITU HYDROGENATION; BIMETALLIC CATALYST; HYDRODEOXYGENATION; DIMETHYLFURAN; CONVERSION; REDUCTION; METHANOL; ACID;
D O I
10.1039/d1se00499a
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
The facile fabrication of low-cost and high-activity catalysts for selective hydrogenolysis of 5-hydroxymethylfurfural (5-HMF) to 2,5-dimethylfuran (2,5-DMF) using renewable and economical ethanol as a hydrogen donor is still a significant challenge. In this work, beta-Mo2C embedded in carbon microspheres was prepared facilely by hydrothermal synthesis with the composite of ammonium molybdate and glucose, and subsequent one-pot solid-state thermolysis under a N-2 atmosphere. The optimal beta-Mo2C embedded in carbon microspheres achieved a high 2,5-DMF yield of 91.6% from 5-HMF selective hydrogenolysis with ethanol as a hydrogen donor under the optimized reaction conditions. Also, the optimal catalyst exhibited good recycling stability with slight loss of activity during four reuse runs. The chemical structure of the catalysts was characterized using multiple techniques. beta-Mo2C nanoparticles were demonstrated to be active sites for 5-HMF hydrogenolysis reactions, while the synergism between beta-Mo2C nanoparticles and their adjacent deficient carbon enhanced the H-2 evolution via ethanol decomposition and hydrogenolysis reaction.
引用
收藏
页码:4749 / 4757
页数:9
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