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Amphiphilic organosilane-directed synthesis of crystalline zeolite with tunable mesoporosity

Authors
Choi, MinkeeCho, Hae SungSrivastava, RajendraVenkatesan, ChithravelChoi, Dae-HeungRyoo, Ryong
Issue Date
Sep-2006
Publisher
NATURE PUBLISHING GROUP
Citation
NATURE MATERIALS, v.5, no.9, pp 718 - 723
Pages
6
Journal Title
NATURE MATERIALS
Volume
5
Number
9
Start Page
718
End Page
723
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/65413
DOI
10.1038/nmat1705
ISSN
1476-1122
1476-4660
Abstract
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.
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Cho, Hae Sung
자연과학대학 (화학과)
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