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Synthesis and characterization of functionalized mesoporous silica by aerosol-assisted self-assembly
被引:78
作者:
Ji, XL
Hu, QY
Hampsey, JE
Qiu, XP
Gao, LX
He, JB
Lu, YF
[1
]
机构:
[1] Tulane Univ, Dept Chem & Biomol Engn, New Orleans, LA 70118 USA
[2] Chinese Acad Sci, Changchun Inst Appl Chem, Polymer Engn Lab, Changchun 130022, Peoples R China
基金:
美国国家科学基金会;
关键词:
D O I:
10.1021/cm052764p
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:
An efficient, productive, and low-cost aerosol-assisted self-assembly process has been developed to produce organically modified mesoporous silica particles via a direct co-condensation of silicate species and organosilicates that contain nonhydrolyzable functional groups in the presence of templating surfactant molecules. Different surfactants including cetyltrimethylammonium bromide, nonionic surfactant Brij-56, and triblock copolymer P123 have been used as the structure-directing agents. The organosilanes used in this study include tridecafluoro-1, 1,2,2-tetrahydrooctyltriethoxysilane, methytriethoxysilane, vinyltrimethoxysilane, and 3-(trimethoxysilyl)propyl methacrylate. X-ray diffraction and transmission electron microscopy studies indicate the formation of particles with various mesostructures. Fourier transform infrared and solid-state nuclear magnetic resonance spectra confirm the organic ligands are covalently bound to the surface of the silica framework. The porosity, pore size, and surface area of the particles were characterized using nitrogen adsorption and desorption measurements. This method provides a direct synthesis route to efficiently synthesize a large variety of organic functionalized mesoporous silica particles with controlled pore sizes, pore surface chemistry.. and pore structures for catalyst, filler, and other applications.
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页码:2265 / 2274
页数:10
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