Selective hydrogenolysis of biomass-derived furfuryl alcohol into 1,2-and 1,5-pentanediol over highly dispersed Cu-Al2O3 catalysts

被引:86
作者
Liu, Hailong [1 ,2 ]
Huang, Zhiwei [1 ]
Kang, Haixiao [1 ]
Xia, Chungu [1 ]
Chen, Jing [1 ]
机构
[1] Chinese Acad Sci, LICP, Suzhou Res Inst LICP, State Key Lab Oxo Synth & Select Oxidat, Lanzhou 730000, Gansu, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
Furfuryl alcohol; 1,2-Pentanediol; 1,5-Pentanediol; Selective hydrogenolysis; Cu-Al catalyst; SILICA-SUPPORTED COPPER; FUEL ADDITIVES; CYCLIC ETHERS; HYDROGENATION; CONVERSION; TRANSFORMATION; CHEMICALS; EFFICIENT; ACID; 1,2-PENTANEDIOL;
D O I
10.1016/S1872-2067(15)61080-4
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Cu nanoparticles supported on a variety of oxide supports, including SiO2, TiO2, ZrO2, Al2O3, MgO and ZnO, were investigated for the hydrogenolysis of biomass-derived furfuryl alcohol to 1,2-pentanediol and 1,5-pentanediol. A Cu-Al2O3 catalyst with 10 wt% Cu loading prepared by a co-precipitation method exhibited the best performance in terms of producing pentanediols compared with the other materials. This catalyst generated an 85.8% conversion and a 70.3% combined selectivity for the target pentanediols at 413 K and 8 MPa H-2 over an 8-h reaction. The catalyst could also be recycled over repeated reaction trials without any significant decrease in productivity. Characterizations with X-ray diffraction, NH3/CO2-temperature programmed desorption, N-2 adsorption, transmission electron microscopy and N2O chemisorption demonstrated that intimate and effective interactions between Cu particles and the acidic Al2O3 support in this material greatly enhanced its activity and selectivity. The promotion of the hydrogenolysis reaction was found to be especially sensitive to the Cu particle size, and the catalyst with Cu particles 1.9 to 2.4 nm in size showed the highest turnover frequency during the synthesis of pentanediols. (C) 2016, Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:700 / 710
页数:11
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