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US4256722A Expired / Lapsed US ⏱️ 0.0 years remaining

Process for producing porous spinel materials

Assignee: Corning Glass Works
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Filing: 1979-11-15
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Granted: 1981-03-17
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Expires: 1999-11-15
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Abstract

Abstract The instant invention is related to the production of porous spinel materials which exhibit exceptional durability in both acid and basic solutions, and possess high porosity with high surface area and narrow range of pore size. More specifically, the present invention is directed to the production of porous spinel materials involving the impregnation of finely-divided trivalent metal oxides, usually Al2O3, Fe2O3, or Cr2O3, with a solution of a divalent metal ion-containing compound, commonly selected from the group of Mg+2, Fe+2, Mn+2, and Zn+2, and thereafter firing the mixture to effect reaction, resulting in the conversion of the trivalent metal oxide to a spinel.

Inventors

  • 👤 Gerald B. Carrier

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-05 18:00
CPC Classifications
C; C01; C01G; C01G49/00; C01G49/0018; C01G49/0072; B; B01; B01J; B01J23/00; B01J23/005; B01J35/00; B01J35/60; B01J37/00; B01J37/12; B01J37/14; C01B; C01B13/00; C01B13/14; C01B13/18; C01B13/185; C01F; C01F7/00; C01F7/02; C01F7/04; C01G37/00; C01G37/14; C01G49/0036; C01G49/0063; C01G9/00; B01D; B01D2239/00; B01D2239/04; B01D2239/0464; B01D2239/0471; B01D2239/10; B01D2239/12; B01D2239/1216; B01D2239/125; B01J35/61; B01J35/613; B01J35/615; B01J35/64; B01J35/647; B01J35/651; B01J35/66; B01J35/67; C01P; C01P2002/00; C01P2002/30; C01P2002/32; C01P2004/00; C01P2004/01; C01P2004/03; C01P2006/00; C01P2006/12; C01P2006/16

Claims Analysis

Total Claims: 7
Claim 1
Independent Claim 274 words
A method for preparing porous bodies consisting essentially of spinel and/or crystals isostructural with spinel having an average pore size between about 450-700 A, about 80% of said pores being within about ±25% of the average pore size, and having a surface area between about 10-75 meters 2 /gram, said crystals having the general formula AO.B 2 O 3 wherein A represents a divalent metal ion and B represents a trivalent metal ion, which comprises the steps of: (a) impregnating a porous, trivalent metal ion-containing material having a surface area between about 50-500 meters 2 /gram, said trivalent metal ion being selected from the group of Al +3 , Fe +3 , and Cr +3 , with a solution of a divalent metal ion-containing compound, said divalent metal ion being selected from the group of Mg +2 , Fe +2 , Mn +2 , and Zn +2 , which compound, upon pyrolysis, will be converted to the respective oxide or other compound capable of reacting with said trivalent metal ion-containing material, said divalent metal ion-containing compound being present in a quantity sufficient to produce an amount of the corresponding divalent metal oxide or other compound ranging from about, by weight, 5% below to about 10% above that required to stoichiometrically react with said trivalent metal ion-containing material; (b) drying the impregnated material; and (c) firing the dried material at a temperature of at least 800° C., but not higher than about 1250° C., for a period of time sufficient to cause essentially complete reaction between said trivalent metal ion-containing material and said divalent metal ion-containing material to form spinel and/or crystals isostructural with spinel.
Claim 2
Independent Claim 274 words
A method for preparing porous bodies consisting essentially of spinel and/or crystals isostructural with spinel having an average pore size between about 450-700 A, about 80% of said pores being within about ±25% of the average pore size, and having a surface area between about 10-75 meters 2 /gram, said crystals having the general formula AO.B 2 O 3 wherein A represents a divalent metal ion and B represents a trivalent metal ion, which comprises the steps of: (a) impregnating a porous, trivalent metal ion-containing material having a surface area between about 50-500 meters 2 /gram, said trivalent metal ion being selected from the group of Al +3 , Fe +3 , and Cr +3 , with a solution of a divalent metal ion-containing compound, said divalent metal ion being selected from the group of Mg +2 , Fe +2 , Mn +2 , and Zn +2 , which compound, upon pyrolysis, will be converted to the respective oxide or other compound capable of reacting with said trivalent metal ion-containing material, said divalent metal ion-containing compound being present in a quantity sufficient to produce an amount of the corresponding divalent metal oxide or other compound ranging from about, by weight, 5% below to about 10% above that required to stoichiometrically react with said trivalent metal ion-containing material; (b) drying the impregnated material; and (c) firing the dried material at a temperature of at least 800° C., but not higher than about 1250° C., for a period of time sufficient to cause essentially complete reaction between said trivalent metal ion-containing material and said divalent metal ion-containing material to form spinel and/or crystals isostructural with spinel.
Claim 3
Dependent Claim 13 words
A method according to claim 1 wherein said solution is an aqueous solution.
Claim 4
Dependent Claim 52 words
A method according to claim 1 wherein said divalent metal ion-containing compound is selected from the group consisting of magnesium acetate, magnesium iodide, magnesium nitrate, magnesium salicylate, magnesium thiosulfate, zinc acetate, zinc perchlorate, zinc iodide, zinc nitrate, zinc sulfate, ferous acetate, ferrous chloride, ferrous nitrate, manganese acetate, manganese chloride, and manganese nitrate.
Claim 5
Dependent Claim 24 words
A method according to claim 1 wherein said impregnation is conducted at a temperature between the freezing point and boiling point of the solution.
Claim 6
Dependent Claim 21 words
A method according to claim 1 wherein said drying is conducted at a temperature below the boiling point of the solution.
Claim 7
Dependent Claim 35 words
A method according to claim 1 wherein said firing is conducted at a temperature between about 900°-1100° C. where the reaction product is magnesium spinel and about 850°-1000° C. where the reaction produce is gahnite.

References Cited (Backward Citations)

US2703789A Cited
US3423194A Cited
US3948808A Cited
US3909455A Cited
US3998939A Cited
US4097300A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1984-03-16 1984-09-15 1985-03-17 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1988-03-16 1988-09-15 1989-03-17 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1992-03-16 1992-09-15 1993-03-17 $7700.00 Window Closed / Lapsed

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