Three-Dimensionally Hierarchical Pt/C Nanocomposite with Ultra-High Dispersion of Pt Nanoparticles as a Highly Efficient Catalyst for Chemoselective Cinnamaldehyde Hydrogenation

被引:39
作者
Hu, Duo [1 ]
Fan, Wenqian [1 ]
Liu, Zhi [1 ]
Li, Ling [1 ]
机构
[1] Liaoning Normal Univ, Fac Chem & Chem Engn, Huanghe Rd 850, Dalian, Peoples R China
基金
中国国家自然科学基金;
关键词
cinnamaldehyde hydrogenation; heterogeneous catalysis; hierarchical pores; nanocomposites; Pt nanoparticles; SUPPORTED PLATINUM CATALYSTS; ORDERED MACROPOROUS LAFEO3; SELECTIVE HYDROGENATION; POROUS CARBON; HIGH-PERFORMANCE; UNSATURATED ALDEHYDES; NANOTUBES; REDUCTION; ADSORPTION; NITROGEN;
D O I
10.1002/cctc.201701301
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
A monolithic carbon-supported Pt nanocomposite with an interconnected three-dimensionally hierarchical porous carbon framework and ultra-high dispersion of Pt nanoparticles (Pt/3DHPC) is synthesized by using an effective liquid phase impregnation template" strategy. The obtained Pt/3DHPC possesses rich mesoporosity and a low amount of oxygen-containing functional groups, which notably improve the accessible internal surface area of macropores, number of active Pt sites, and electron transfer ability. When used as a catalyst for the selective cinnamaldehyde (CMA) hydrogenation towards cinnamyl alcohol (CMO), Pt/3DHPC exhibits high CMA conversion (92.7%) and CMO selectivity (91.1%) at 1 h reaction time, and the corresponding activity (1553.7 h(-1)) greatly surpasses not only the single-sized mesoporous carbon and microporous activated carbon-supported counterparts but also the previously reported Pt catalysts dispersed on other forms of carbon. Furthermore, Pt/3DHPC can be reused at least fifteen times without pronounced decay owing to the strong interaction between Pt and carbon. The present work demonstrates the validity of multiscale control in carbon-supported Pt catalysts by overall consideration of the mass transportation, and the accessibility, quantity, and capability of active sites towards chemoselective hydrogenation of CMA, which is expected to be extended to other catalysis-related processes.
引用
收藏
页码:779 / 788
页数:10
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