Raney Ni-Si Catalysts for Selective Hydrogenation of Highly Concentrated 2-Butyne-1,4-diol to 2-Butene-1,4-diol

被引:35
|
作者
Chen, Xiao [1 ]
Zhang, Mingming [1 ]
Yang, Kaixuan [1 ]
Williams, Christopher T. [2 ]
Liang, Changhai [1 ]
机构
[1] Dalian Univ Technol, Lab Adv Mat & Catalyt Engn, Dalian 116024, Peoples R China
[2] Univ S Carolina, Dept Chem Engn, Columbia, SC 29208 USA
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Raney Ni-Si; Silicification; 2-Butyne-1,4-diol; Selective hydrogenation; SUPERCRITICAL CARBON-DIOXIDE; NICKEL-CATALYSTS; SLURRY REACTOR; MASS-TRANSFER; PHENYLACETYLENE; INTERMETALLICS; BUTYNEDIOL; NANOWIRES; KINETICS;
D O I
10.1007/s10562-014-1259-8
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
Raney Ni-Si catalysts were synthesized by treating Raney Ni with silane in a fluidized bed reactor and tested in the selective hydrogenation of 2-butyne-1,4-diol (BYD) at high concentration. Structural characterizations including XRD patterns, TEM images, and X-ray photoelectron spectroscopy show that Raney Ni-Si catalysts are composed of a Ni core surrounded by nickel silicides. These species transform from Ni-rich silicide (Ni2Si) to Si-rich silicide (NiSi2) with increasing silicification temperature from 250 A degrees C to 450 A degrees C. The insertion of Si atoms into Raney Ni catalysts decreased the catalytic activity, but significantly improved the selectivity to 2-butene-1,4-diol (BED). The beneficial effect of Si on the selectivity hydrogenation of BYD may be caused by the presence of Si at Ni-defect sites, and the formation of the surface nickel silicide that suppress the further hydrogenation of BED. Compared with the traditional Lindlar-type catalysts, such Raney Ni-Si materials can be used extensively in organic synthesis for selective hydrogenation of alkynes, avoiding the associated hazards of toxic additives. Raney Ni-Si catalysts, synthesized by treating Raney Ni with silane, showed that the insertion of Si atoms into Raney Ni catalysts decreased the catalytic activity, but significantly improved the selectivity to 2-butene-1,4-diol.
引用
收藏
页码:1118 / 1126
页数:9
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