Synthesis and characterization of mesoporous mordenite

被引:205
作者
Li, Xianfeng [1 ,2 ]
Prins, Roel [1 ]
van Bokhoven, Jeroen Anton [1 ]
机构
[1] ETH, Swiss Fed Inst Technol, Inst Chem & Bioengn, CH-8093 Zurich, Switzerland
[2] China Univ Petr, Fac Chem Sci & Engn, Beijing 102249, Peoples R China
基金
瑞士国家科学基金会;
关键词
Mesopore; Mordenite; Leaching; Alkylation; Isomerization; Diffusivity; ALUMINUM COORDINATION; CATALYTIC CRACKING; ZEOLITE-BETA; ACID; FRAMEWORK; ZSM-5; DEALUMINATION; SILICA; RATIO; ISOMERIZATION;
D O I
10.1016/j.jcat.2009.01.001
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
Three methods were investigated to synthesize mesoporous mordenite. XRD, N-2 physisorption, SEM, and TEM showed that the mordenite obtained by acid leaching followed by base leaching of a conventional mordenite is a crystalline mesoporous material with MOR framework. The higher diffusivity of toluene indicated that mesopores benefited molecule transport through the zeolite crystal. Measurement of the number of Brensted acid sites by n-propylamine TPD and Al-27 NMR showed that the mesoporous mordenite had less extra-framework aluminum and a large number of Brensted acid sites, while the isomerization of 2-methyl-2-pentene indicated that the mesoporous mordenite possessed a higher reactivity than conventional mordenite. The mesoporous mordenite had a much higher catalytic activity than conventional mordenite in the alkylation of benzene with benzyl alcohol. At 353 K and under atmospheric pressure, the conversion of benzyl alcohol over hierarchical mesoporous mordenite was 100% in 3 h, whereas the conversion over conventional mordenite was less than 2%. Synthesis of mesoporous mordenite with amphiphilic organosilane and carbon as secondary template did not give real mesoporous mordenite. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:257 / 265
页数:9
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