Shape-selective alkylation and related reactions of mononuclear aromatic hydrocarbons over H-ZSM-5 zeolites modified with lanthanum and cerium oxides

被引:70
|
作者
Sugi, Y [1 ]
Kubota, Y
Komura, K
Sugiyama, N
Hayashi, A
Kim, JH
Seo, G
机构
[1] Gifu Univ, Fac Engn, Dept Mat Sci & Engn, Gifu 5011193, Japan
[2] Chonnam Natl Univ, Dept Appl Chem Engn, Kwangju 500757, South Korea
[3] Chonnam Natl Univ, Res Inst Catalysis, Kwangju 500757, South Korea
基金
日本学术振兴会;
关键词
H-ZSM-5; La2O3 and CeO2 modification; deactivation of external acid sites; para-selectivity; alkylation;
D O I
10.1016/j.apcata.2005.10.024
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 La2O3 and CeO2 modifications of H-ZSM-5 zeolites were examined to improve the shape-selectivity in the alkylation of mononuclear aromatic hydrocarbons and related reactions. The selectivities of p-diethylbenzene (p-DEB) among diethylbenzene isomers were improved without significant loss of catalytic activity by the modification with these oxides in the ethylation of ethylbenzene (EB). The La2O3 modification enhanced the selectivities of p-DEB more effectively than the CeO2 modification. The improvement of the selectivities over these oxides is due to the prevention of the isomerization of p-DEB at external acid sites. The para-selectivity for La2O3-modified H-ZSM-5 zeolites is improved due to "product selectivity" resulting from the preferential diffusion of p-DEB by the adjustment of pore entrance as well as by the deactivation of external acid sites. The enhancement of the formation of less bulky xylene isomer was also observed in the disproportionation of toluene and the isomerization of xylene isomers over La2O3- and CeO2-modified H-ZSM-5 zeolites. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:157 / 166
页数:10
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