Synthesis of mesoporous silica spheres under quiescent aqueous acidic conditions

被引:197
作者
Yang, H [1 ]
Vovk, G [1 ]
Coombs, N [1 ]
Sokolov, I [1 ]
Ozin, GA [1 ]
机构
[1] Univ Toronto, Dept Chem, Mat Chem Res Grp, Toronto, ON M5S 3H6, Canada
关键词
D O I
10.1039/a705746f
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
A gyroid-to-sphere shape transition has been unveiled in the growth of mesoporous silica morphologies that are synthesized under quiescent acidic aqueous conditions. It can be induced by a decrease of the acidity for a surfactant-based gyroid preparation. As the acidity is gradually lowered from the gyroid domain, the growth process changes from one involving a smooth continuous deposition of silicate-surfactant micellar solute species onto specific regions of an evolving silicate liquid crystal seed, to one in which deposition instead occurs on non-specific regions of the seed. This creates multigranular gyroid morphologies which at lower acidity emerge as sphere shapes. The gyroid-to-sphere metamorphosis appears to correlate with an acidity and/or temperature dependent switch in the mode of formation, from the gyroid involving fast and local polymerization of a growing silicate liquid crystal seed, to the sphere based upon a slower and global polymerization of a silicate liquid crystal droplet. Surface tension will cause such a droplet to adopt a spherical shape, ultimately to be rigidified in the-form of a mesoporous silica sphere. Comparative gyroid and sphere information is presented on synthesis-size-shape-channel plan relations, degree of orientational order of the channels, extent of polymerization of the silica, thermal stability and nitrogen adsorption properties. The ability to synthesize 1-10 mu m diameter mesoporous silica spheres with a narrow sphere size and pore size distribution portends a myriad of applications in large molecule catalysis, chromatographic separations and nanocomposites.
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页码:743 / 750
页数:8
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