Ni-Co nano-alloys confined by N-doped porous carbon overlayer to boost hydrodeoxygenation of 5-hydroxymethylfurfural

被引:1
|
作者
Bao, Yuan [1 ]
Pu, Weijia [2 ]
Zhang, Yiwei [1 ]
Xiao, Yahui [1 ]
Liu, Yong [2 ]
机构
[1] Henan Univ, Henan Engn Res Ctr Resource & Energy Recovery Wast, Sch Energy Sci & Technol, Zhengzhou 450046, Peoples R China
[2] Henan Univ, Sch Energy Sci & Technol, Henan Key Lab Polyoxometalate Chem, Zhengzhou 450046, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
N -doped carbon; Ni-Co alloy; 5-Hydroxymethylfurfural; Hydrodeoxygenation; SELECTIVE HYDROGENATION; CATALYTIC TRANSFORMATION; DIRECT CONVERSION; BIOMASS; CHEMICALS; METAL; 2,5-DIMETHYLFURAN; NANOTUBES; SURFACE;
D O I
10.1016/j.jece.2024.114914
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Ni-Co nano-alloys confined by in-situ formed N-doped porous carbon overlayer have been prepared through chelation of metal cations with citric acid and urea followed by carbonization for hydrodeoxygenation of 5hydroxymethylfurfural (HMF) into 2, 5-dimethylfuran (DMF). The results indicated that the Ni-Co nano-alloys were formed and homogeneously distributed within the N-doped porous carbon overlayer. The electronic effect of the Ni-Co nano-alloys significantly boosted hydrodeoxygenation activity of the Co2Ni1@NC catalyst and simultaneously inhibited further hydrogenation and opening of furan ring. The N-doped porous carbon overlayer around Ni-Co nano-alloys not only facilitated to disperse and stable Ni-Co nano-alloys through strong metal- support interaction, but also protected the Ni-Co nano-alloys from aggregation. Therefore, the Co2Ni1@NC catalyst offered superior catalytic performance with the HMF conversion of 100 % and DMF selectivity of 93.0 %. Moreover, the Co2Ni1@NC catalyst displayed excellent stability without significant activity loss after five recycles due to the spatial confinement of N-doped carbon overlayer.
引用
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页数:10
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