Claims
- 1. The process for the preparation of a cracking catalyst comprising the treatment of a zeolitic aluminosilicate which has a mole ratio of oxides in the dehydrated state of
- (0.85-1.1) M.sub.2/n O:Al.sub.2 O.sub.3 ; xSiO.sub.2
- wherein M is a cation having a valence of "n" and "x" has a value greater than 6.0; has an x-ray powder diffraction pattern having at least the d-spacings of Table A and having extraneous silicon atoms in the crystal lattice in the form of framework SiO.sub.4 tetrahedra by employing at least one of the following steps of:
- (i) treating the aluminosilicate at an effective temperature for an effective time;
- (ii) providing an effective amount of at least one multivalent cation selected from the class consisting of cerium, lanthanum, praseodymium, neodymium, promethium, samarium, europium, gadolinium, terbium, dysprosium, holmium, erbium, thulium, ytterbium, lutetium and mixtures thereof; with the proviso that steps (i) and (ii) can be carried out for one or more times in any order.
- 2. The process of claim 1 wherein the aluminosilicate is ammonium exchanged one or more times.
- 3. The process of claim 1 wherein step (i) is employed.
- 4. The process of claim 1 wherein step (ii) is employed.
- 5. The process of claim 1 wherein steps (i) and (ii) are employed.
- 6. The process according to claim 1 wherein "x" has a value greater than 8.0.
- 7. The process of claim 1 wherein the aluminosilicate is heated at an effective temperature and for an effective time in the presence of steam.
- 8. The process of claim 7 wherein the effective time is greater than 0.1 hour.
- 9. The process of claim 8 wherein the effective time is between 0.1 hour and about 10 hours.
- 10. The process of claim 1 wherein the zeolitic aluminosilicate is ion exchanged with at least one multivalent cation in an amount of between 16 ion exchange percent and 90 ion exchange percent.
- 11. The process of claim 1 wherein the step (ii) is employed and the multivalent cation is selected from the group consisting of cerium, lanthanium, praseodymium, neodymium, promethium, samarium, europium, gadolinium, terbium, dysprosium, holmium, erbium, thulium, ytterbium, lutetium and mixtures thereof.
- 12. The process of claim 1 wherein the zeolitic aluminosilicate is defined as having a chemical composition expressed in terms of mole fractions of framework tetrahedra as:
- [Al.sub.(a-N) Si.sub.b+(N-.DELTA.z) .quadrature..sub.z ]O.sub.2
- wherein ##EQU4## has a value greater than 6 and the change in defect structure factor .DELTA.z is less than 0.08; an increased silicon content in the framework, (N-.DELTA.z)/N, of at least 0.5; a+b+z=1; (a-N)+[b+(N-.DELTA.z)]+z=1; and a cation equivalent expressed as a monovalent cation species, M.sup.+ /Al, from 0.85 to 1.1 and the characteristic crystal structure of zeolite Y as indicated by an X-ray powder diffraction pattern having at least the d-spacings set forth broadly in Table A.
- 13. The catalyst prepared by the process of claim 1.
- 14. The catalyst prepared by the process of claim 2.
- 15. A cracking catalyst comprising: (1) an effective amount of a zeolitic aluminosilicate having a mole ratio of oxides in the dehydrated state of
- (0.85-1.1) M.sub.2/n O:Al.sub.2 O.sub.3 :xSiO.sub.2
- wherein M is a cation having a valence of "n" and "x" has a value greater than 6.0; has an x-ray powder diffraction pattern having at least the d-spacings of Table A; has extraneous silicon atoms in the crystal lattice in the form of framework SiO.sub.4 tetrahedra; wherein said zeolitic aluminosilicate has at least 2 ion exchange percent of the cations selected from the group consisting of cerium, lanthanum, praseodymium, neodymium, promethium, samarium, europium, gadolinium, terbium, dysprosium, holmium, erbium, thulium, ytterbium, lutetium and mixtures thereof; (2) and at least one inorganic oxide matrix component.
- 16. The cracking catalyst of claim 15 wherein the value of "x" is greater than 6.0 and less than 8.0.
- 17. The cracking catalyst of claim 15 wherein the zeolitic aluminosilicate is defined as having a chemical composition expressed in terms of mole fractions of framework tetrahedra as:
- [Al.sub.(a-N) Si.sub.b+(N-.DELTA.z) .quadrature..sub.z ]O.sub.2
- wherein ##EQU5## has a value greater than 6.0 and the change in defect structure factor .DELTA.z is less than 0.08; an increased silicon content in the framework, (N-.DELTA.z)/N, of at least 0.5; a+b+z=1; (a-N)+[b+(N-.DELTA.z)]+z=1; and a cation equivalent expressed as a monovalent cation species, M.sup.+ /Al, from 0.85 to 1.1 and the characteristic crystal structure of zeolite Y as indicated by an X-ray powder diffraction pattern having at least the d-spacings set forth broadly in Table A.
- 18. The cracking catalyst of claim 17 wherein the change in defect structure factor .DELTA.z is less than 0.05.
- 19. The cracking catalyst of claim 17 wherein ##EQU6## has a value greater than 6.0 and less than 8.0.
- 20. The catalyst of claim 15 wherein said zeolitic aluminosilicate contains between about 5 and about 80 ion exchange percent of a multivalent cation selected from the group consisting of cerium, lanthanum, praseodymium, neodymium, promethium, samarium, europium, gadolinium, terbium, dysprosium, holmium, erbium, thulium, ytterbium, lutetium and having less than 1.2 percent by weight Na.sub.2 O, based on the weight of said zeolitic aluminosilicate; wherein said zeolitic aluminosilicate has not been calcined.
- 21. The catalyst of claim 20 wherein said zeolitic aluminosilicate has less than 0.8 percent by weight Na.sub.2 O based on the weight of the zeolitic aluminosilicate.
CROSS REFERENCE TO RELATED APPLICATION
Thie application is a continuation in part application of U.S. Ser. No. 490,965, filed May 2, 1983 now abandoned.
US Referenced Citations (1)
Number |
Name |
Date |
Kind |
4503023 |
Breck |
Mar 1985 |
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Continuation in Parts (1)
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Number |
Date |
Country |
Parent |
490965 |
May 1983 |
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