Demonstrates the effective creation of stable mesoporous silica in various conditions, suggesting enhanced synthesis methods.
Highly ordered and hydrothermally stable cubic mesoporous silicas SBA-1 ( P m 3̅ n mesophase) have been synthesized over a broad temperature range using tetraethoxysilane (TEOS) and cetyltriethylammonium bromide (CTEABr) as silicon source and template agent, respectively, under highly acidic conditions via addition of sugar molecules such as d -fructose or sucrose as an auxiliary agent. Various synthesis parameters such as d -fructose content, acid concentration and reaction time have been optimized under different synthesis conditions in order to obtain highly ordered mesoporous silica SBA-1 materials with good hydrothermal stability. In contrast to the conventional synthesis methods requiring low synthesis temperature, this strategy allows the preservation of the SBA-1 mesophase under high temperature synthesis conditions and leads to a highly cross-linked silica framework. In particular, the framework locations of the derivatives of d -fructose molecules and their interactions with the surfactant molecules were investigated by two-dimensional 1 H− 1 H exchange NMR. The present NMR results confirmed that the derivatives of d -fructose are in close spatial proximity to the surfactant molecules to form stable spherical micelles with adequate curvatures for the formation of cubic mesophase in a wide range of synthesis conditions.
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Ting et al. (2010) studied this question.
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