Synthesis of crystalline ultra-large pore oxide materials
AssigneeMobil Oil Corporation
InventorsDavid C. Calabro, John Hen
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Abstract
There is provided a method for preparing crystalline ultra-large pore oxide materials. The materials are formed from reaction mixtures comprising an amphiphilic compound, such as a cetyltrimethylammonium compound, a source of at least one oxide, such as silica, and water. The concentration of amphiphilic compounds in these reaction mixtures is rather low. The addition of an inorganic salt, such as sodium bromide, to the reaction mixture may result in the increased thermal stability of the as-synthesized form of the crystalline material and may also alter the crystalline phase of the product.
Claims17
A method for preparing a composition of matter comprising an inorganic, crystalline phase exhibiting an X-ray diffraction pattern with at least one peak at a position greater than about 18 Angstrom Units d-spacing with a relative intensity of 100, and a benzene adsorption capacity of greater than about 15 grams benzene per 100 grams anhydrous crystal at 50 torr and 25.degree. C., said method comprising the steps of:
- (a) forming a reaction mixture comprising an amphiphilic compound, a source of at least one oxide and water, wherein the molar ratio of amphiphilic compound to water is less than 0.004;
- (b) maintaining said reaction mixture under sufficient conditions to form a crystalline oxide material;
- and
- (c) recovering said crystalline oxide material.
A method for preparing a composition of matter comprising an inorganic, crystalline phase exhibiting, after calcination, an X-ray diffraction pattern with at least one peak at a position greater than about 18 Angstrom Units d-spacing with a relative intensity of 100, and a benzene adsorption capacity of greater than about 15 grams benzene per grams anhydrous crystal at 50 torr and 25.degree. C., said method comprising the steps of:
- (a) forming a reaction mixture comprising an amphiphilic compound, a source of at least one oxide and water, wherein the molar ratio of amphiphilic compound to water is less than 0.004;
- (b) maintaining said reaction mixture under sufficient conditions to form a crystalline oxide material;
- (c) recovering said crystalline oxide material in as-synthesized form comprising residual amphiphilic compound, said as-synthesized form of said material having an X-ray diffraction pattern with at least one peak at a position greater than about 18 Angstrom Units d-spacing with a relative intensity of 100, said as-synthesized form of said material not being stable to calcination conditions sufficient to remove said residual amphiphilic compound;
- (d) stabilizing said material from step (c) to calcination conditions by treating said material from step (c) with a compound of the formula
- M'X'.sub.2 Y'm
- where M' is boron, aluminum, silicon or titanium;
- X' represents alkyl halides having from 1-6 carbon atoms and/or alkoxides having 1-6 carbon atoms;
- Y' represents X' and/or alkyls with 1-12 carbon atoms;
- and m=1-2;
- and
- (e) calcining said material from step (d) under conditions sufficient to remove residual organic compounds.
A method for preparing a composition of matter comprising an inorganic, crystalline phase exhibiting, after, calcination, an X-ray diffraction pattern with at least one peak at a position greater than about 18 Angstrom Units d-spacing with a relative intensity of 100, and a benzene adsorption capacity of greater than about 15 grams benzene per grams anhydrous crystal at 50 torr and 25.C, said method comprising the steps of:
- (a) forming a reaction mixture comprising an amphiphilic compound, a source of at least one oxide, an inorganic salt, and water, wherein the molar ratio of amphiphilic compound to water is less than 0.004;
- (b) maintaining said reaction mixture under sufficient conditions to form a crystalline oxide material;
- (c) recovering said crystalline oxide material in as-synthesized form comprising residual amphiphilic compound, said as-synthesized form of said material having an X-ray diffraction pattern with at least one peak at a position greater than about 18 Angstrom Units d-spacing with a relative intensity of 100, said as-synthesized form of said material being stable to calcination conditions sufficient to remove said residual amphiphilic compound;
- (d) calcining said material from step (c) under conditions sufficient to remove said residual amphiphilic compound.
Dependencies are inferred from the claim text.