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AssigneeBoard of Trustees operating Michigan State University
InventorsThomas J. Pinnavaia, Peter T. Tanev, Wenzhong Zhang, Jialiang Wang, Malama Chibwe
Estimating the term…
A neutral templating route to mesoporous molecular sieves based on H-bonding and self-assembly between neutral primary amine or diamine surfactants (S°) and neutral inorganic precursors (I°) has been used to prepare hexagonal and lamellar mesoporous silicas with site isolated transition metal centers. This templating approach allows for the preparation of hexagonal or hexagonal-like mesoporous oxidation catalysts with large framework wall thickness of at least about 17 Å, small elementary particle size (≦400 Å), and unique combinations of framework-confined mesopores and textural mesopores while at the same time providing for facile recovery of the neutral template by simple solvent extraction. The templating of neutral metallosilicate precursors (I°) with neutral diamine surfactants (S°—S°) affords thermally stable pillared lamellar metallosilicates exhibiting complementary framework-confined microporosity and textural mesoporosity while at the same time also providing for template recovery by solvent extraction. In addition, a hexagonal transition metal-substituted catalysts, analogous to MCM-41, have been prepared using the mediated S+X·I+ templating pathway (Pathway 3) and mild reaction conditions. These new mesoporous metallosilicate molecular sieves exhibit exceptional catalytic activity for peroxide hydroxylation of benzene and oxidation of substituted aromatics with kinetic diameters that are too large (larger than 6 Å) to access the pore structure of the conventional microporous transition metal-substituted molecular sieves such as titano- and vanadosilicates.
A lamellar pillared mesoporous metal silicate composition, wherein the metal is present in place of some of the silicon in the silicate and capable of undergoing a change of oxidation number in an oxidation or reduction reaction with an organic molecule having a kinetic diameter greater than 6 Å, the composition directly prepared by a neutral self-assembly method which comprises reacting a neutral bipolar diamine template and neutral inorganic oxide precursors in the presence of hydrolyzing agent as a solvent and optionally with a co-solvent with the hydrolyzing agent to form a reaction product, aging of the reaction mixture at reaction conditions which form the crystalline pillared lamellar metal silicate and removing of the template, the hydrolyzing agent and optional co-solvent, wherein the pillared lamellar silicate composition exhibits a lamellar x-ray diffraction pattern selected from the group consisting of FIGS. 2, 4, 10, 11 and 12, and having N2 adsorption-desorption isotherm and Horvath Kawazoe pore distribution as shown in FIG. 13.
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