Claims
- 1. A catalytic cracking process comprising contacting a hydrocarbonaceous feed at catalytic cracking conditions with a catalyst comprising a Y-type crystalline aluminosilicate zeolite prepared from a clay starting material, a residue derived from said clay, and at least about 0.1 weight percent phosphorus, based on the weight of said zeolite plus residue, said Y-type crystalline aluminosilicate zeolite having the structure of faujasite and having a silica to alumina mole ratio of at least about 3:1, said catalyst having been prepared initially by the steps which comprise:
- (a) ion-exchanging a clay derived alkali metal-containing Y-type crystalline aluminosilicate zeolite and the clay derived residue with a cation other than an alkali metal to decrease the alkali metal content of said alkali metal-containing zeolite;
- (b) calcining the resulting ion-exchanged zeolite and clay derived residue, and
- (c) contacting the resulting calcined zeolite and clay-derived residue with a medium comprising an anion selected from the group consisting of dihydrogen phosphate anion, dihydrogen phosphite anion and mixtures thereof for a time sufficient to composite said amount of phosphorus with said calcined zeolite and residue.
- 2. The catalytic process of claim 1 wherein said catalyst comprises clay in addition to said clay-derived residue.
- 3. The catalytic cracking process of claim 1 wherein said catalyst additionally comprises an inorganic oxide selected from the group consisting of silica, alumina, silica-alumina, zirconia, boria, titania, magnesia, and mixtures thereof.
- 4. The catalytic cracking process of claim 1 wherein said catalyst comprises at least about 0.2 weight percent of said phosphorus, based on the weight of said zeolite plus residue.
- 5. The catalytic cracking process of claim 1 wherein said catalyst comprises from about 2 to about 70 weight percent of said zeolite.
- 6. The catalytic cracking process of claim 1 wherein said calcination is conducted at conditions such as to decrease the unit cell size of said zeolite by an amount ranging from about 0.05 angstroms to about 0.10 angstroms from an initial unit cell size of above about 24.5 angstroms.
- 7. The catalytic cracking process of claim 1 wherein said calcination is conducted at a temperature ranging from about 500.degree. F. to about 1400.degree. F.
- 8. The catalytic cracking process of claim 1 wherein said anion is derived from a phosphorus-containing component selected from the group consisting of inorganic acid of phosphorus, salts of inorganic acid of phosphorus and mixtures thereof.
- 9. The catalytic cracking process of claim 1 wherein said anion is derived from a phosphorus-containing component selected from the group consisting of phosphorous acid (H.sub.3 PO.sub.3), phosphoric acid (H.sub.3 PO.sub.4), salts of phosphorous acid, salts of phosphoric acid and mixtures thereof.
- 10. The catalytic cracking process of claim 1 wherein said anion is a dihydrogen phosphate anion derived from monoammonium phosphate, diammonium phosphate and mixtures thereof.
- 11. The catalytic cracking process of claim 1 wherein said contacting step with said anion is conducted at a pH ranging from 2 to 8.
- 12. The catalytic cracking process of claim 1 wherein said catalytic cracking conditions include a temperature ranging from about 750.degree. to about 1300.degree. F. and a pressure ranging from about 0 to about 150 psig.
- 13. The process of claim 1 wherein said catalyst comprises from about 0.1 weight percent to about 0.8 weight percent of said phosphorus, based on the weight of said zeolite plus residue.
Parent Case Info
This is a division of application Ser. No. 381,388, filed May 24, 1982, now U.S. Pat. No. 4,454,241.
US Referenced Citations (7)
Divisions (1)
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Number |
Date |
Country |
Parent |
381388 |
May 1982 |
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