氢解
催化作用
镍
双功能
化学
金属
无机化学
有机化学
化学工程
材料科学
工程类
作者
Xiao Kong,Yulong Zhu,Hongyan Zheng,Xianqing Li,Yulei Zhu,Yongwang Li
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2015-09-04
卷期号:5 (10): 5914-5920
被引量:151
标识
DOI:10.1021/acscatal.5b01080
摘要
Hydrogenolysis of carbon–oxygen bonds is a versatile synthetic method, of which hydrogenolysis of bioderived 5-hydroxymethylfurfural (HMF) to furanic fuels is especially attractive. However, low-temperature hydrogenolysis (in particular over non-noble catalysts) is challenging. Herein, nickel nanoparticles (NPs) inlaid nickel phyllosilicate (NiSi-PS) are presented for efficient hydrogenolysis of HMF to yield furanic fuels at 130–150 °C, being much superior with impregnated Ni/SiO2 catalysts prepared from the same starting materials. NiSi-PS also shows a 2-fold HMF conversion intrinsic rate and 3-fold hydrogenolysis rate compared with the impregnated Ni/SiO2. The superior performance originated from the synergy of highly dispersed nickel NPs and substantially formed acid sites due to coordinatively unsaturated Ni (II) sites located at the remnant nickel phyllosilicate structure, as revealed by detailed characterizations. The model reactions over the other reference catalysts further highlighted the metal–acid synergy for hydrogenolysis reactions. NiSi-PS can also efficiently catalyze low-temperature hydrogenolysis of bioderived furfural and 5-methylfurfural, demonstrating a great potential for other hydrogenolysis reactions.
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