Synthesis, characterization, and catalytic properties of zeolites IM-5 and NU-88

被引:68
作者
Lee, SH
Lee, DK
Shin, CH [1 ]
Park, YK
Wright, PA
Lee, WM
Hong, SB
机构
[1] Chungbuk Natl Univ, Dept Chem Engn, Chungbuk 361763, South Korea
[2] Korea Res Inst Chem Technol, Div Chem Technol, Taejon 305606, South Korea
[3] Univ St Andrews, Sch Chem, St Andrews KY16 9ST, Fife, Scotland
[4] Hanbat Natl Univ, Div Chem Engn, Taejon 305719, South Korea
基金
新加坡国家研究基金会;
关键词
zeolites IM-5 and NU-88; pore topologies; synthesis; characterization; catalytic evaluation;
D O I
10.1016/S0021-9517(02)00178-1
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
The synthesis, characterization, and catalytic properties of two high-silica zeolites IM-5 and NU-88, whose structures still remain unresolved, are presented. When the 1,5-bis(N-methylpyrrolidinium)pentane and 1,6-bis(N-methylpyrrolidinium)hexane cations are used as organic structure-directing agents, respectively, crystallization of pure IM-5 and NU-88 was possible only from synthesis mixtures with a narrow range of SiO2/Al2O3 and NaOH/SiO2 ratios. The overall characterization results of this study strongly suggest that IM-5 is a new multidimensional large-pore zeolite, whereas NU-88 is a nanocrystalline material that could be an intergrowth of several hypothetical polymorphs in the beta family of zeolites. Despite its nanocrystalline nature, however, no detectable extraframework Al species were found to exist in H-NU-88, revealing excellent thermal stability. H-IM-5 and H-NU-88 both exhibit a very high 1-butene conversion compared to H-ZSM-35 over the period of time studied here, whereas the opposite holds for the formation of isobutene. This reveals that their pore topologies are large enough to allow undesired side reactions such as 1-butene dimerization followed by cracking to light olefins. They also show the initial n-octane cracking activity comparable to that on H-ZSM-5. However, a notable decrease in n-octane conversion on these two zeolites with increasing time on stream is observed. When the isomerization and cracking activities of all zeolites employed in this study are correlated with their coke-forming propensities, it can be concluded that both materials present a shape-selective character falling within the category of multidimensional, large-pore zeolites. (C) 2003 Elsevier Science (USA). All fights reserved.
引用
收藏
页码:151 / 170
页数:20
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