Multifunctional Pd@UiO-66 Catalysts for Continuous Catalytic Upgrading of Ethanol to n-Butanol

被引:111
作者
Jiang, Dahao [1 ]
Fang, Geqian [1 ]
Tong, Yuqin [1 ]
Wu, Xianyuan [1 ]
Wang, Yifan [1 ]
Hong, Dongsen [1 ]
Leng, Wenhua [1 ]
Liang, Zhe [1 ]
Tu, Pengxiang [1 ]
Liu, Liu [1 ]
Xu, Kaiyue [1 ]
Ni, Jun [1 ]
Li, Xiaonian [1 ]
机构
[1] Zhejiang Univ Technol, Inst Ind Catalysis, Hangzhou 310014, Zhejiang, Peoples R China
来源
ACS CATALYSIS | 2018年 / 8卷 / 12期
关键词
multifunctional catalysts; Pd nanoparticles; metal-organic framework; Lewis acids; ethanol upgrading; METAL-ORGANIC FRAMEWORK; SYNERGISTIC CATALYSIS; CONDENSATION; UIO-66; 1-BUTANOL; EFFICIENT; ACID; ALCOHOLS; DESIGN; SITES;
D O I
10.1021/acscatal.8b04014
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
UiO-66-encapsulated nanopalladium (Pd@UiO-66) catalysts were used as highly efficient and stable catalysts for continuous catalytic upgrading of ethanol to n-butanol. The best Pd@UiO-66 catalyst exhibited 49.8% of ethanol conversion, 48.6% of selectivity toward n-butanol, and thereby 24.2% of n-butanol yield at relatively low temperature (523 K) and pressure (2 MPa) during a 200 h long-term evaluation. The high catalytic activity and selectivity of Pd@UiO-66 catalyst are primarily ascribed to the close synergy of highly dispersed Pd nanoparticles and coordinatively unsaturated Zr sites on Zr-6 nodes of UiO-66, as active centers for dehydrogenation/hydrogenation and aldol condensation, respectively; however, the high stability of the catalyst is mainly attributed to the electrostatic attraction of Pd nanoparticles with Zr-6 nodes and the confinement effect of the cavities of UiO-66.
引用
收藏
页码:11973 / 11978
页数:11
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