Construction of Cu-Ru bimetallic catalyst for the selective catalytic transfer hydrogenation of carbonyl (C--O) in biomass-derived compounds

被引:1
|
作者
Cai, Bo [1 ,2 ,3 ]
Kang, Rui [2 ]
Feng, Junfeng [2 ]
Eberhardt, Thomas L. [4 ]
Ma, Zhongqing
Zhu, Qingge [1 ]
Pan, Hui [2 ]
机构
[1] Zhejiang A&F Univ, Coll Chem & Mat Engn, Natl Engn Res Ctr Wood Based Resource Comprehens U, Hangzhou 311300, Peoples R China
[2] Nanjing Forestry Univ, Int Innovat Ctr Forest Chem & Mat, Nanjing 210037, Peoples R China
[3] Southwest Forestry Univ, Int Joint Res Ctr Biomass Mat, Kunming 650224, Peoples R China
[4] USDA Forest Serv, Forest Prod Lab, One Gifford Pinchot Dr, Madison, WI 53726 USA
关键词
Biomass conversion; Catalytic transfer hydrogenation; Bimetallic catalyst; Carbonyl compounds; Effects of heteroatom; GAMMA-VALEROLACTONE; ETHYL LEVULINATE; ACID; CONVERSION; EFFICIENT; NI; HYDRODEOXYGENATION; RUTHENIUM; OXIDATION; ESTERS;
D O I
10.1016/j.renene.2023.119833
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The catalytic transfer hydrogenation (CTH) of levulinate ester to gamma-valerolactone is one of the important reactions for production of renewable fuels from biomass. An efficient and robust bimetallic Cu-Ru catalyst were developed for the hydrogenation of biomass-derived ethyl levulinate to gamma-valerolactone. A series of bimetallic catalysts were prepared and characterized in detail. Subsequently, the as-prepared catalysts were evaluated in the hydrogenation system of ethyl levulinate. The results showed that Cu-Ru/ZrO2-SO3-SiO2-450 catalyst provided 100 % GVL yield in 12 h at 180 degrees C. Meanwhile, it also exhibited high catalytic hydrogenation activity for the various biomass-derived carbonyl compounds. The structure-reactivity relationship of catalysts was investigated in detail, and the results show the interaction between support and metal sites played an important role in the hydrogenation activity. The sulfur species could tune the electronic states of metallic sites to gain optimal activity. Besides, the Cu-Ru/ZrO2-SO3-SiO2-450 catalyst performed excellent recyclability in five reaction runs without an obvious loss of activity.
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页数:11
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