US5250282A
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Use of amphiphilic compounds to produce novel classes of crystalline oxide materials
Assignee: ExxonMobil Oil Corp
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Filing: 1992-10-27
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Granted: 1993-10-05
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Expires: 2012-10-27
Abstract
Abstract There is provided a process for using amphiphilic compounds in preparing new classes of crystalline oxide materials. These oxide materials may have uniformly large pores, e.g., having a size of about 40 Angstoms in diameter. This process involves combining sources of oxides with micellar solutions of organic amphiphilic compounds, such as quaternary ammonium cationic surfactants. Aggregates of these micelles in the form of liquid crystals are believed to function as templates for the formation of the present highly porous, crystalline materials.
Inventors
- 👤 Charles T. Kresge
- 👤 Michael E. Leonowicz
- 👤 Wieslaw J. Roth
- 👤 James C. Vartuli
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-11-03 12:29
CPC Classifications
C; C10; C10G; C10G47/00; C10G47/02; C10G47/10; C10G47/12; C10G47/16; B; B01; B01D; B01D53/00; B01D53/34; B01D53/74; B01D53/86; B01D53/8621; B01D53/8625; B01D53/8628; B01J; B01J20/00; B01J20/02; B01J20/04; B01J20/041; B01J20/06; B01J20/08; B01J20/10; B01J20/103; B01J20/12; B01J20/16; B01J20/18; B01J20/30; B01J20/3078; B01J29/00; B01J29/03; B01J29/0308; B01J29/04; B01J29/041; C01; C01B; C01B37/00; C01B37/02; C01B37/06; C01B37/08; C01B39/00; C10G11/00; C10G11/02; C10G11/04; C10G11/05; B01J2229/00; B01J2229/10; B01J2229/26; B01J2229/30; B01J2229/32; B01J2229/34; B01J2229/36; B01J2229/40; B01J2229/42
Claims Analysis
Total Claims: 2
Claim 1
Independent Claim
223 words
A process for using an amphiphilic compound to prepare a highly porous crystalline oxide material 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° C., said process comprising the steps of: (a) preparing a reaction mixture capable of forming a precursor to said crystalline oxide material, said reaction mixture comprising one or more sources of at least one oxide, a solvent or solvent mixture and an amphiphilic compound; (b) maintaining said mixture under sufficient conditions of pH, temperature and time for formation of a crystalline oxide containing residual amphiphilic compound; (c) recovering said crystalline oxide containing residual amphiphilic compound from step (b); and (d) calcining said recovered material from step (c) under conditions sufficient to remove residual amphiphilic compound, wherein said amphiphilic compound is a cetyltrimethylammonium compound, and wherein said reaction mixture of step (a) has the mole ratio Solvent/(R'.sub.2 O+M.sub.2 O) of greater than 92, where R' is said amphiphilic compound and M is alkali metal or alkali earth metal, and wherein the calcined material from step (d) has a hexagonal electron diffraction pattern and a pore size of at least 13 Angstroms.
Claim 2
Dependent Claim
223 words
A process for using an amphiphilic compound to prepare a highly porous crystalline oxide material 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° C., said process comprising the steps of: (a) preparing a reaction mixture capable of forming a precursor to said crystalline oxide material, said reaction mixture comprising one or more sources of at least one oxide, a solvent or solvent mixture and an amphiphilic compound; (b) maintaining said mixture under sufficient conditions of pH, temperature and time for formation of a crystalline oxide containing residual amphiphilic compound; (c) recovering said crystalline oxide containing residual amphiphilic compound from step (b); and (d) calcining said recovered material from step (c) under conditions sufficient to remove residual amphiphilic compound, wherein said amphiphilic compound is a cetyltrimethylammonium compound, and wherein said reaction mixture of step (a) has the mole ratio Solvent/(R'.sub.2 O+M.sub.2 O) of greater than 92, where R' is said amphiphilic compound and M is alkali metal or alkali earth metal, and wherein the calcined material from step (d) has a hexagonal electron diffraction pattern and a pore size of at least 13 Angstroms.
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| 3.5 Years (Year 4) | 1996-10-04 | 1997-04-05 | 1997-10-05 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 2000-10-04 | 2001-04-05 | 2001-10-05 | $3760.00 | Window Closed / Lapsed |
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