IP Library Granted Patent US 11,213,810
Granted Patent B1
US 11,213,810 · App. 16/921,124 · Granted Jan 4, 2022

Method of producing a cracking catalyst

Inventors: Lianhui Ding (Dhahran, SA); Manal Al-Eid (Dhahran, SA)
Assignee: Saudi Arabian Oil Company
B01J29/7007B01J6/001B01J21/04B01J21/08B01J23/16B01J23/30B01J23/75B01J29/7215B01J29/7615B01J35/0006B01J35/023B01J35/1019B01J35/1023B01J35/1042B01J35/1047B01J35/1061B01J37/0009B01J37/0018B01J37/0045B01J37/0201B01J37/04B01J37/08C10G11/05C10G47/04C10G47/16C10G47/20B01J23/28B01J23/755B01J2229/20B01J2229/42C10G47/02C10G2300/70
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Quick Facts
Patent No.
US 11,213,810
App. No.
16/921,124
Granted
Jan 4, 2022
Kind
B1
Abstract

Embodiments of the present disclosure are directed to a method of producing a cracking catalyst. The method of producing a cracking catalyst may comprise producing a plurality of uncalcined zeolite-beta nanoparticles via a dry-gel method, directly mixing the plurality of uncalcined zeolite-beta nanoparticles with at least one additional hydrocracking component to form a mixture, and calcining the mixture to form the cracking catalyst. The plurality of uncalcined zeolite-beta nanoparticles may have an average diameter of less than 100 nm.

Claims (26)

1. A method of producing a cracking catalyst, the method comprising:

producing a plurality of uncalcined zeolite-beta nanoparticles via a dry-gel method, wherein the plurality of uncalcined zeolite-beta nanoparticles has an average diameter of less than 100 nm;

directly mixing the plurality of uncalcined zeolite-beta nanoparticles with at least one additional hydrocracking component to form a mixture; and

calcining the mixture to form the cracking catalyst; wherein the plurality of uncalcined zeolite-beta nanoparticles has not been subjected to centrifugation before being mixed with the at least one additional hydrocracking component.

2. The method of producing a cracking catalyst of claim 1 , wherein the plurality of uncalcined zeolite-beta nanoparticles has not been subjected to centrifugation above 3,000 rpm, before being mixed with the at least one additional hydrocracking component.

3. The method of producing a cracking catalyst of claim 1 , wherein the plurality of uncalcined zeolite-beta nanoparticles has not been subjected to calcination above 200° C. for more than 30 minutes, before being mixed with the at least one additional hydrocracking component.

4. The method of producing a cracking catalyst of claim 1 , wherein the at least one additional hydrocracking component comprises one or more of MoO 3 , WO 3 , NiO, large pore alumina, ZSM-5, zeolite-Y, tungsten precursors, amorphous silica-alumina, and binders.

5. The method of producing a cracking catalyst of claim 1 , wherein the cracking catalyst comprises from 14 wt. % to 16 wt. % MoO 3 , 4 wt. % to 6 wt. % NiO, 10 wt. % to 50 wt. % of the zeolite-beta nanoparticles, 0 wt. % to 40 wt. % zeolite-Y, 0 wt. % to 20 wt. % large pore alumina, and 15 wt. % to 20 wt. % of a binder.

6. The method of producing a cracking catalyst of claim 1 , wherein the mixture is calcined at 400° C. to 700° C. for 1 hour to 10 hours.

7. The method of producing a cracking catalyst of claim 1 , wherein the directly mixing comprises extrusion.

8. The method of producing a cracking catalyst of claim 1 , wherein the directly mixing comprises both extrusion and impregnation.

9. The method of producing a cracking catalyst of claim 1 , wherein the cracking catalyst is impregnated with metal compounds after the mixture is calcined to form an impregnated cracking catalyst support.

10. The method of producing a cracking catalyst of claim 9 wherein the impregnated cracking catalyst support is further calcined.

11. The method of producing a cracking catalyst of claim 1 , wherein the plurality of uncalcined zeolite-beta nanoparticles has an average diameter from 20 nm to 50 nm.

12. The method of producing a cracking catalyst of claim 1 , wherein at least 90% of the plurality of uncalcined zeolite-beta nanoparticles have diameters from 20 nm to 50 nm.

13. The method of producing a cracking catalyst of claim 1 , wherein an average pore size of the plurality of uncalcined zeolite-beta nanoparticles is from 3 nm to 10 nm.

14. The method of producing a cracking catalyst of claim 1 , wherein a microporous surface area of the plurality of uncalcined zeolite-beta nanoparticles is from 300 m 2 /g to 500 m 2 /g.

15. The method of producing a cracking catalyst of claim 1 , wherein a BET surface area of the plurality of uncalcined zeolite-beta nanoparticles is from 500 m 2 /g to 700 m 2 /g.

16. The method of producing a cracking catalyst of claim 1 , wherein a pore volume of the plurality of uncalcined zeolite-beta nanoparticles is from 0.8 ml/g to 0.9 ml/g.

17. The method of producing a cracking catalyst of claim 1 , wherein the producing the plurality of uncalcined zeolite-beta nanoparticles via the dry-gel method comprises:

combining an alumina source, a structure directing agent, and a silica source to form a slurry;

optionally, introducing NaOH to the slurry such that the final concentration of NaOH in the slurry is from 0.000001 g/L to 0.1 g/L;

drying the slurry to form a dry-gel; and

autoclaving the dry-gel in a humidified autoclave to form an uncalcined zeolite-beta.

18. The method of producing a cracking catalyst of claim 17 , wherein the water content of the dry-gel is less than 25 wt. %.

19. The method of producing a cracking catalyst of claim 17 , wherein the dry-gel is not agitated during autoclaving.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 6, 2020
From: DING, LIANHUI; AL-EID, MANAL
To: SAUDI ARABIAN OIL COMPANY
Reel/Frame 053125/0771 →
Cited By (2)
US 12,239,966 US 12,594,547