Enhancing catalytic transfer semi-hydrogenation of alkynes over N-doped carbon-supported Pd-Ni bimetallic catalysts

被引:0
|
作者
Xiong, Yanru [1 ]
Qian, Weisai [1 ]
He, Junwen [1 ]
Huang, Lizhi [1 ]
Wang, Zezhe [1 ]
Tan, Weile [1 ]
Chen, Zhaofeng [3 ]
Li, Ao [1 ]
Guo, Haoquan [1 ]
Wei, Qinhong [1 ,2 ]
机构
[1] Zhejiang Ocean Univ, Sch Petrochem Engn & Environm, Dept Chem Engn, Zhoushan 316022, Zhejiang, Peoples R China
[2] Zhejiang Prov Key Lab Petrochem Pollut Control, Zhoushan 316022, Zhejiang, Peoples R China
[3] Yancheng Inst Technol, Sch Informat Engn, Yancheng 224051, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Bimetallic catalyst; N-doped carbon; Phenylacetylene; Semi-hydrogenation; SELECTIVE SEMIHYDROGENATION; PHASE HYDROGENATION; PALLADIUM SULFIDE; PARTICLE-SIZE; SURFACE; NANOPARTICLES; ADSORPTION; ACETYLENE; DESIGN; SITES;
D O I
10.1007/s11164-025-05505-8
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Olefin is a crucial chemical intermediate that is in high demand for polymer production. The catalytic alkyne semi-hydrogenation process represents a promising avenue for industrial purification of olefins. Herein, we report the findings of a study investigating the transfer of alkyne semi-hydrogenation over a bimetallic catalyst, in which Pd nanoparticles and highly dispersed Ni atoms were anchored onto graphite-like C3N4 with nitrogen defects. The optimal Pd0.14Ni0.01 catalyst was used for intermolecular semi-hydrogenation of alkynes in conjunction with sodium borohydride. Nitrogen defects heightened the catalytic activity by modifying the electron density distribution and accelerating charge transfer from Pd to C3N4. Furthermore, the synergism of the Pd-Ni bimetallic positions facilitated the generation of the intermediate styrene and accelerated the rate-determining step. This study provides novel insights into the design of streamlined high-performance semi-hydrogenated catalysts.
引用
收藏
页码:1371 / 1387
页数:17
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