Amphiphilic organosilane-directed synthesis of crystalline zeolite with tunable mesoporosity

被引:1089
作者
Choi, Minkee
Cho, Hae Sung
Srivastava, Rajendra
Venkatesan, Chithravel
Choi, Dae-Heung
Ryoo, Ryong [1 ]
机构
[1] Korea Adv Inst Sci & Technol, Natl Creat Res Initiat Ctr Funct Nanomat, Taejon 305701, South Korea
[2] Korea Adv Inst Sci & Technol, Dept Chem, Taejon 305701, South Korea
关键词
MOLECULAR-SIEVES; SINGLE-CRYSTALS; SILICA; SEEDS; MESOSTRUCTURES; FRAMEWORKS; STABILITY; ACIDITY; MCM-48; CARBON;
D O I
10.1038/nmat1705
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
Zeolites are a family of crystalline aluminosilicate materials widely used as shape-selective catalysts, ion exchange materials, and adsorbents for organic compounds(1,2). In the present work, zeolites were synthesized by adding a rationally designed amphiphilic organosilane surfactant to conventional alkaline zeolite synthesis mixtures. The zeolite products were characterized by a complementary combination of X-ray diffraction (XRD), nitrogen sorption, scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The analyses show that the present method is suitable as a direct synthesis route to highly mesoporous zeolites. The mesopore diameters could be uniformly tailored, similar to ordered mesoporous silica with amorphous frameworks(3). The mesoporous zeolite exhibited a narrow, small-angle XRD peak, which is characteristic of the short-range correlation between mesopores, similar to disordered wormhole-like mesoporous materials(4,5). The XRD patterns and electron micrographs of the samples taken during crystallization clearly showed the evolution of the mesoporous structure concomitantly to the crystallization of zeolite frameworks. The synthesis of the crystalline aluminosilicate materials with tunable mesoporosity and strong acidity has potentially important technological implications for catalytic reactions of large molecules, whereas conventional mesoporous materials lack hydrothermal stability and acidity.
引用
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页码:718 / 723
页数:6
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