The role of nitride species in the gas-phase furfural hydrogenation activity of supported nickel catalysts

被引:9
|
作者
Pilar Jimenez-Gomez, Carmen [1 ]
Defilippi, Chiara [2 ]
Antonio Cecilia, Juan [1 ]
Moreno-Tost, Ramon [1 ]
Maireles-Torres, Pedro [1 ]
Giordano, Cristina [2 ]
机构
[1] Univ Malaga, Dept Quim Inorgan Cristalog & Mineral, Unidad Asociada ICP CSIC, Campus Teatinos, E-29071 Malaga, Spain
[2] Queen Mary Univ London, Chem Dept, Sch Biol & Chem Sci, Mile End Rd, London E1 4NS, England
关键词
Nickel nitride; Furfuryl alcohol; Hydrogenation; Furfural; Biorefinery; SELECTIVE HYDROGENATION; NI; CONVERSION; METAL; CHEMICALS; KINETICS; PLATFORM; ALCOHOL; SURFACE;
D O I
10.1016/j.mcat.2020.110889
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
A series of C-rich nickel nitride nanoparticles supported on silica has been prepared by the urea glass route, with urea as nitrogen and carbon source, and characterized by different physico-chemical techniques. They consist of Ni3N nanoparticles of 20-25 nm embedded into a carbonaceous matrix. These catalysts are much more active and stable than a nickel supported silica catalyst, which drastically deactivates. The supported Ni3N catalyst with a 10 wt.% Ni maintained a furfural conversion higher than 80 % after 5 h of time-on-stream, at 170 degrees C, with a high WHSV of 6 h(-1). Complete initial furfural conversion values were observed at reaction temperatures varying from 170 to 230 degrees C, and the selectivity toward furan and furfuryl alcohol (decarbonylation and hydrogenation products, respectively) was tuned by varying this temperature. After the catalytic tests, XPS and XRD have demonstrated that nanoparticles are stable, although carbonaceous deposits were also detected.
引用
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页数:12
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