Amphiphilic organosilane-directed synthesis of crystalline zeolite with tunable mesoporosity

介孔材料 沸石 材料科学 硅酸铝 结晶 化学工程 介孔有机硅 无定形固体 分子筛 水热合成 透射电子显微镜 扫描电子显微镜 热液循环 催化作用 纳米技术 介孔二氧化硅 有机化学 化学 复合材料 工程类
作者
Minkee Choi,Hae Sung Cho,Rakesh K. Srivastava,C. Venkatesan,Dae‐Heung Choi,Ryong Ryoo
出处
期刊:Nature Materials [Springer Nature]
卷期号:5 (9): 718-723 被引量:1145
标识
DOI:10.1038/nmat1705
摘要

Zeolites are a family of crystalline aluminosilicate materials widely used as shape-selective catalysts, ion exchange materials, and adsorbents for organic compounds. 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. 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. 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.
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