Morphological effect of β zeolite nanocrystallite aggregates as the support of Pt catalyst for the hydroisomerization of n-heptane

被引:5
作者
Yao, Yue [1 ]
Wang, Jianhong [1 ]
Deng, Yanyan [1 ]
Wang, Jun [1 ]
机构
[1] Nanjing Univ Technol, State Key Lab Mat Oriented Chem Engn, Coll Chem & Chem Engn, Nanjing 210009, Peoples R China
基金
中国国家自然科学基金;
关键词
Hydroisomerization of n-heptane; Bifunctional catalyst; beta Zeolite; Pt catalyst; Nanocrystalline; MOLECULAR-SIEVES; DEALUMINATED USY; PD/H-BETA; ISOMERIZATION; ACIDITY; OCTANE; MORDENITE; PARAFFINS; PENTANE; HEXANE;
D O I
10.1007/s11144-012-0454-0
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 bifunctional catalyst Pt/H beta-n (Pt loading: 0.4 wt%) was prepared by the impregnation of an aqueous solution of chloroplatinic acid with beta zeolite, wherein the beta zeolite support has an unusual morphology of egg-like microspheres assembled by nanocrystallites. Other two control catalysts were also prepared using a beta support with micro-sized crystals and a commercial one with varying crystal sizes. The catalysts were characterized by XRD, SEM, ICP, N-2 sorption isotherms and mesopore size distribution, and evaluated in the hydroisomerization of n-heptane in an atmospheric fixed bed flow reactor. Though Pt/H beta-n has similar acidity and Pt loading (0.4 wt%) to the two control catalysts, it exhibits remarkably higher conversion of n-heptane and selectivity to isomerization. According to the characterization data, the higher activity of Pt/H beta-n is the result of the faster diffusion of reactants in shorter channels of nanocrystallines and the uniformly distributed mesopores within the microspheres.
引用
收藏
页码:167 / 177
页数:11
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