Highly dispersed Pd nanoparticles confined in ZSM-5 zeolite crystals for selective hydrogenation of cinnamaldehyde

被引:16
|
作者
Alfilfil, Lujain [1 ]
Ran, Jiansu [2 ,3 ]
Chen, Cailing [1 ]
Dong, Xinglong [1 ]
Wang, Jianjian [2 ,3 ]
Han, Yu [1 ]
机构
[1] King Abdullah Univ Sci & Technol KAUST, Adv Membranes & Porous Mat AMPM Ctr, Phys Sci & Engn Div, Thuwal 239556900, Saudi Arabia
[2] Chongqing Univ, Multiscale Porous Mat Ctr, Inst Adv Interdisciplinary Studies, Chongqing 400045, Peoples R China
[3] Chongqing Univ, Sch Chem & Chem Engn, Chongqing 400045, Peoples R China
基金
中国国家自然科学基金;
关键词
Selective hydrogenation; Cinnamaldehyde; Pd-confined catalyst; Dry-gel conversion; CHEMOSELECTIVE HYDROGENATION; PRODUCT SELECTIVITY; CINNAMYL ALCOHOL; FINE CHEMICALS; CATALYSTS; OXIDES; EFFICIENT; CLUSTERS; MFI; AU;
D O I
10.1016/j.micromeso.2021.111566
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Selective hydrogenation of alpha,beta-unsaturated aldehyde catalyzed by supported Pd nanoparticles (NPs) is challenging, especially under harsh reaction conditions. Here, we report a facile method to prepare a catalyst composed of highly dispersed Pd NPs (similar to 2.6 nm) confined in zeolite ZSM-5 crystals. When used in the hydrogenation of cinnamaldehyde, the prepared catalyst (Pd@SG-ZSM-5) exhibited excellent performance for the selective production of hydrocinnamaldehyde (HCAL) due to the confinement effect. Compared with the traditional supported Pd catalyst prepared by impregnation, Pd@SG-ZSM-5 showed a 2.5-fold enhancement in the HCAL selectivity (73% vs. 30%). Liquid adsorption combined with infrared spectroscopy characterization revealed that compared with the traditional catalyst, Pd@SG-ZSM-5 adsorbed much less reactant as well as product molecules and desorbed the generated HCAL quickly, thereby suppressing the formation of by-products and leading to high selectivity of HCAL.
引用
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页数:5
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