Surface Synergetic Effects of Ni-ReOx for Promoting the Mild Hydrogenation of Furfural to Tetrahydrofurfuryl Alcohol

被引:35
|
作者
Lin, Wei [2 ]
Chen, Yi [2 ]
Zhang, Yuexing [1 ]
Zhang, Yongsheng [2 ]
Wang, Jianshe [2 ]
Wang, Liucheng [2 ]
Xu, Chunbao Charles [3 ]
Nie, Renfeng [2 ]
机构
[1] Dezhou Univ, Coll Chem & Chem Engn, Dezhou 253023, Peoples R China
[2] Zhengzhou Univ, Henan Ctr Outstanding Overseas Scientists, Sch Chem Engn, Natl Key Lab Biobased Transportat Fuel Technol, Zhengzhou 450001, Peoples R China
[3] City Univ Hong Kong, Sch Energy & Environm, Kowloon, Hong Kong, Peoples R China
关键词
ReOx-decorated Ni-based catalysts; synergetic effect; hydrogen spillover; C=O activation; furfural hydrogenation; HIGHLY SELECTIVE HYDROGENATION; CATALYTIC-HYDROGENATION; EFFICIENT; NANOPARTICLES; BIOMASS; ACID;
D O I
10.1021/acscatal.3c01217
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
Ni-ReOx bimetallic catalysts (Ni-ReOx/TiO2) were prepared through a successive impregnation method, which is extremely active in furfural (FAL) hydrogenation to tetrahydrofurfuryl alcohol (THFOL) under mild reaction conditions. For instance, high FAL initial reaction rate (439.4 mmol/g-Ni/h) and THFOL formation rate (80.4 mmol/g-Ni/h) were achieved over Ni-5ReO(x)/TiO2, which are 13.2 and 6.6 times higher than those of Ni/TiO2, respectively. The unique catalyst reactivity derives from rich Lewis acidic ReOx and intimate electron interaction of ReOx with Ni NPs. Kinetic studies reveal that ReOx decoration decreases the activation barrier of -C=O hydrogenation other than the furan ring. Mechanism studies show that ReOx has a good affinity for C=O and H-2 and favors hydrogen spillover and C=O bond activation on Ni, thus reinforcing the synergistic effect of Ni and ReOx. This catalyst is versatile for various furan aldehydes and is relatively stable for 5 times recycling, showing relative potential for industrial application.
引用
收藏
页码:11256 / 11267
页数:12
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