TY - JOUR
T1 - Synthesis of mesoporous silica spheres under quiescent aqueous acidic conditions
AU - Yang, Hong
AU - Vovk, Gregory
AU - Coombs, Neil
AU - Sokolov, Igor
AU - Ozin, Geoffrey A.
PY - 1998
Y1 - 1998
N2 - 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 μm 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.
AB - 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 μm 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.
UR - http://www.scopus.com/inward/record.url?scp=0001751203&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0001751203&partnerID=8YFLogxK
U2 - 10.1039/a705746f
DO - 10.1039/a705746f
M3 - Article
AN - SCOPUS:0001751203
SN - 0959-9428
VL - 8
SP - 743
EP - 750
JO - Journal of Materials Chemistry
JF - Journal of Materials Chemistry
IS - 3
ER -