The synergistic effect of Cu0 and Cu+ for one-step synthesis of aviation biofuel from biomass-derived ketones

被引:5
|
作者
Li, Tan [1 ]
Su, Jing [1 ]
Yin, Linjia [1 ]
Zhang, Xiangkun [1 ]
Wang, Cong [1 ]
Li, Xinbao [2 ]
Zhang, Jing [3 ]
Wang, Kaige [1 ]
机构
[1] Zhejiang Univ, State Key Lab Clean Energy Utilizat, Hangzhou 310027, Peoples R China
[2] Ningbo Univ, Fac Maritime & Transportat, Ningbo 315211, Peoples R China
[3] East China Univ Sci & Technol, State Key Lab Chem Engn, Shanghai 200237, Peoples R China
基金
中国国家自然科学基金;
关键词
FUEL RANGE ALKANES; SELECTIVE HYDRODEOXYGENATION; CATALYSTS; CYCLOPENTANONE; ACID; CYCLOHEXANOLS; CONDENSATION; CONVERSION; REDUCTION; CHEMICALS;
D O I
10.1039/d3gc02671j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A Cu-based catalyst was developed for one-step solvent-free synthesis of aviation biofuel from biomass-derived ketones, including acetone, cyclopentanone, cyclohexanone, and 2-pentanone. Under the optimal working conditions, the conversion rate of acetone, cyclopentanone, cyclohexanone and 2-pentanone of 100% can be achieved by using Cu/Al2O3. 79.7 c% maximum carbon yield of liquid hydrocarbons with 89.5% selectivity of aviation biofuel was obtained under the conditions of 1.0 MPa H-2, 280 degrees C, and 2 h(-1) WHSV. The effects of the calcination temperature on the acidity and basicity of the catalyst, as well as the valence and dispersion of Cu species, were investigated. Based on DFT calculations and in situ DRIFTS results, the preferred adsorption of carbonyl groups and efficient dissociation of hydrogen on Cu+ increased the local concentration of H and feedstock on the catalyst surface, accelerating the rate-determining step that predominated on Cu-0. The synergistic effect of Cu-0 and Cu+ enhanced the formation of aviation biofuel.
引用
收藏
页码:1910 / 1926
页数:18
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