Catalytic Performance and Characterization of Anatase TiO2 Supported Pd Catalysts for the Selective Hydrogenation of Acetylene

被引:11
|
作者
Gao Xiao-Ping [1 ,2 ]
Guo Zhang-Long [1 ,2 ]
Zhou Ya-Nan [1 ,2 ]
Jing Fang-Li [1 ]
Chu Wei [1 ,2 ]
机构
[1] Sichuan Univ, Sch Chem Engn, Chengdu 610065, Peoples R China
[2] Sichuan Univ, Inst New Energy & Low Carbon Technol, Chengdu 610207, Peoples R China
关键词
Pd/TiO2; catalyst; Acetylene selective hydrogenation; Anatase TiO2; {101} plane; Structure characterization; EXPOSED; 001; FACETS; EXCESS ETHYLENE; INTERMETALLIC COMPOUNDS; PD-AG/AL2O3; CATALYSTS; PD-AG/TIO2; PALLADIUM CATALYSTS; RU NANOPARTICLES; NANOSCALE CERIA; SHAPE; EFFICIENT;
D O I
10.3866/PKU.WHXB201611251
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
Anatase TiO2 nanospindles containing 89% exposed {101} facets (TiO2-101) and nanosheets with 77% exposed {001} facets (TiO2-001) were hydrothermally synthesized and used as supports for Pd catalysts. The effects of the TiO2 materials on the catalytic performance of Pd/TiO2-101 and Pd/TiO2-001 catalysts were investigated in the selective hydrogenation of acetylene to polymer-grade ethylene. The Pd/TiO2-101 catalyst exhibited enhanced performance in terms of acetylene conversion and ethylene yield. To understand these effects, the catalysts were characterized by H-2 temperature-programmed desorption (H-2-TPD), H-2 temperatureprogrammed reduction (H-2-TPR), transmission electron microscopy (TEM), pulse CO chemisorption, X-ray photoelectron spectroscopy (XPS), and thermogravimetric analysis (TGA). The TEM and CO chemisorption results confirmed that Pd nanoparticles (NPs) on the TiO2-101 support had a smaller average particle size (1.53 nm) and a higher dispersion (15.95%) than those on the TiO2-001 support (average particle size of 4.36 nm and dispersion of 9.06%). The smaller particle size and higher dispersion of Pd on the Pd/TiO2-101 catalyst provided more reaction active sites, which contributed to the improved catalytic activity of this supported catalyst.
引用
收藏
页码:602 / +
页数:15
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