Pore-size dependent catalytic activity of supported Pd catalysts for selective hydrogenation of nitrile butadiene rubber

被引:6
|
作者
Wang, Shidong [1 ]
Wang, Yaxi [1 ]
Wu, Xinru [1 ,2 ]
Hu, Cejun [3 ]
Zhang, Hongwei [1 ]
Cui, Qinyang [1 ]
Bao, Xiaojun [1 ,2 ]
Yuan, Pei [1 ,2 ]
机构
[1] Fuzhou Univ, Coll Chem Engn, Natl Engn Res Ctr Chem Fertilizer Catalyst, Fuzhou 350002, Peoples R China
[2] Qingyuan Innovat Lab, Quanzhou 362801, Peoples R China
[3] Fuzhou Univ, Coll Mat Sci & Engn, Fuzhou 350002, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
Nitrile butadiene rubber; Supported Pd catalysts; Macroporous SiO 2; Hydrogenation; Pore diffusion effect; HOLLOW SILICA MICROSPHERES; PALLADIUM CATALYST; CARBON; FUNCTIONALIZATION; PERFORMANCE; NANOTUBES; NBR;
D O I
10.1016/j.ces.2023.118629
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Pore diffusion effect plays a crucial role in heterogeneous hydrogenation of unsaturated polymers. However, how large pore size can eliminate the pore diffusion limitation remains a controversial issue. Herein, we prepared a series of Pd/SiO2 catalysts with graded pore sizes and investigated the effect of pore size on hydrogenation activity of nitrile butadiene rubber (NBR). It is found that when the catalyst pore size (Dcat) is 7 times of the diameter of NBR chains (DNBR), the Weisz modulus 0 can be reduced to < 0.3 thus the internal mass transfer limitation can be eliminated, making NBR easier to approach the active sites. Consequently, the catalysts with the Dcat/DNBR > 7 exhibit excellent catalytic activity (96.7%) and selectivity (100%) to C = C. This work emphasizes that the pore size of catalysts can regulate the pore transfer limitation and the accessibility of internal active sites, providing useful guidance for the design of efficient macromolecular hydrogenation catalysts. CO 2023 Elsevier Ltd. All rights reserved.
引用
收藏
页数:10
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