Synthesis of Hierarchical MOR-Type Zeolites with Improved Catalytic Properties

被引:7
|
作者
Mcheik, Zeinab [1 ,2 ,3 ,4 ]
Pinard, Ludovic [3 ]
Toufaily, Joumana [4 ]
Hamieh, Tayssir [4 ]
Daou, T. Jean [1 ,2 ]
机构
[1] Univ Haute Alsace UHA, Axe Mat Porosite Controlee MPC, Inst Sci Mat Mulhouse IS2M, UMR 7361,CNRS, F-68093 Mulhouse, France
[2] Univ Strasbourg Unistra, F-67000 Strasbourg, France
[3] CNRS, Inst Chim Milieux & Mat Poitiers, UMR 7285, 4 Rue Michel Brunet,Batiment B27, F-86073 Poitiers 09, France
[4] Lebanese Univ, Lab Mat Catalysis Environm & Analyt Methods, Fac Sci, Sect 1,Campus Raf Hariri, Hadath, Lebanon
来源
MOLECULES | 2021年 / 26卷 / 15期
关键词
zeolites; hierarchical zeolites; mordenite; n-hexane cracking; MORDENITE ZEOLITE; NANOSHEETS; CRYSTALLIZATION; ORGANOSILANE; PERFORMANCE;
D O I
10.3390/molecules26154508
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Hierarchical MOR-type zeolites were synthesized in the presence of hexadecyltrimethylammonium bromide (CTAB) as a porogen agent. XRD proved that the concentration of CTAB in the synthesis medium plays an essential role in forming pure hierarchical MOR-type material. Above a CTAB concentration of 0.04 mol center dot L-1, amorphous materials are observed. These hierarchical mordenite possess a higher porous volume compared to its counterpart conventional micrometer crystals. Nitrogen sorption showed the presence of mesoporosity for all mordenite samples synthesized in the presence of CTAB. The creation of mesopores due to the presence of CTAB in the synthesis medium does not occur at the expense of zeolite micropores. In addition, mesoporous volume and BET surface seem to increase upon the increase of CTAB concentration in the synthesis medium. The Si/Al ratio of the zeolite framework can be increased from 5.5 to 9.1 by halving the aluminum content present in the synthesis gel. These synthesized hierarchical MOR-type zeolites possess an improved catalytic activity for n-hexane cracking compared to large zeolite crystals obtained in the absence of CTAB.
引用
收藏
页数:14
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