Polymer-Supported Pd Nanoparticles for Solvent-Free Hydrogenation

被引:7
|
作者
Luo, Qingsong [1 ,2 ]
Wang, Hai [1 ,2 ]
Xiang, Qian [3 ]
Lv, Yating [1 ,2 ]
Yang, Jiabao [4 ]
Song, Lijuan [4 ]
Cao, Xiaoming [3 ,5 ]
Wang, Liang [1 ,2 ]
Xiao, Feng-Shou [1 ,2 ]
机构
[1] Zhejiang Univ, Key Lab Biomass Chem Engn, Minist Educ, Hangzhou 310058, Peoples R China
[2] Zhejiang Univ, Coll Chem & Biol Engn, Hangzhou 310058, Peoples R China
[3] East China Univ Sci & Technol, Sch Chem & Mol Engn, State Key Lab Green Chem Engn & Ind Catalysis, Shanghai 200237, Peoples R China
[4] Liaoning Petrochem Univ, Key Lab Petrochem Catalyt Sci & Technol, Fushun 113001, Peoples R China
[5] Shanghai Jiao Tong Univ, Sch Chem & Chem Engn, Shanghai 200240, Peoples R China
基金
中国国家自然科学基金;
关键词
SELECTIVE HYDROGENATION; SINGLE ATOMS; CATALYSTS; ACETYLENE; EFFICIENT; CARBON; SEMIHYDROGENATION; PHOSPHORUS; CLUSTERS; REMOVAL;
D O I
10.1021/jacs.4c09241
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Breaking the trade-off between activity and stability of supported metal catalysts has been a long-standing challenge in catalysis, especially for metal nanoparticles (NPs) with high hydrogenation activity but poor stability. Herein, we report a porous poly(divinylbenzene) polymer-supported Pd NP catalyst (Pd/PDVB) with both high activity and excellent stability for the solvent-free hydrogenation of nitrobenzene, even at ambient temperature (25 degrees C) and H-2 pressure (0.1 MPa). Pd/PDVB gave a turnover frequency as high as 22,632 h(-1) at 70 degrees C and 0.4 MPa, exceeding 5556 h(-1) of the classical Pd/C catalyst under equivalent conditions. Mechanistic studies reveal that the polymer support benefits the desorption of the aniline product from the Pd surface, which is crucial for rapid hydrogenation under solvent-free conditions. In addition, the polymer support in Pd/PDVB efficiently hindered Pd leaching, resulting in good stability.
引用
收藏
页码:26379 / 26386
页数:8
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