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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.
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页码:167 / 177
页数:11
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