IP Library Granted Patent US 11,376,573
Granted Patent B2
US 11,376,573 · App. 16/791,554 · Granted Jul 5, 2022

Acidic catalyst

Inventors: James J. Spivey (Baton Rouge, LA); Kunlun Ding (Baton Rouge, LA); Swarom Kanitkar (Morgantown, WV)
Assignee: Board of Supervisors of Louisiana State University and Agricultural and Mechanical College
B01J29/70B01J27/06B01J29/041B01J29/40B01J37/0209C07C2/76C07C5/2705C07C5/2708C07C2521/04C07C2521/08C07C2527/08C07C2527/125C07C2527/126C07C2529/70
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Quick Facts
Patent No.
US 11,376,573
App. No.
16/791,554
Granted
Jul 5, 2022
Kind
B2
Abstract

Methods of preparing an acidic catalyst are disclosed that include heating a metal halide to produce a vapor phase metal halide, contacting an initial support material with the vapor phase metal halide in a reaction vessel causing a first chemical reaction and producing an intermediate acidic catalyst, contacting the intermediate acidic catalyst with HBr causing a second chemical reaction and producing an acidic catalyst product which is both more acidic than the intermediate acidic catalyst and more acidic than the initial support material.

Claims (40)

1. A method of preparing an acidic catalyst comprising:

a. heating a metal halide to produce a vapor phase metal halide;

b. contacting an initial support material with the vapor phase metal halide in a reaction vessel thereby causing a first chemical reaction and thereby producing an intermediate acidic catalyst;

c. wherein the initial support material is selected from an aluminum oxide based catalyst and a silicon oxide based catalyst;

d. wherein the vapor phase metal halide is selected from aluminum trichloride and aluminum tribromide;

e. contacting the intermediate acidic catalyst with HBr thereby causing a second chemical reaction and thereby producing an acidic catalyst product;

f. wherein the acidic catalyst product is more acidic than the intermediate acidic catalyst;

g. wherein the acidic catalyst product is more acidic than the initial support material; and

h. wherein the HBr is gas phase HBr.

2. The method of preparing an acidic catalyst of claim 1 wherein the second chemical reaction takes place at room temperature.

3. The method of preparing an acidic catalyst of claim 1 wherein the second chemical reaction takes place between 50 and 200° C.

4. The method of preparing an acidic catalyst of claim 1 wherein the metal halide is aluminum trichloride and the initial support material is silica gel.

5. The method of preparing an acidic catalyst of claim 1 wherein the metal halide is aluminum tribromide and the initial support material is MCM-41.

6. The method of preparing an acidic catalyst of claim 1 wherein the metal halide is aluminum tribromide and the initial support material is SBA-15.

7. The method of preparing an acidic catalyst of claim 1 wherein the metal halide is aluminum tribromide and the initial support material is ZSM-5.

8. The method of preparing an acidic catalyst of claim 1 wherein the initial support material is MCM-41.

9. The method of preparing an acidic catalyst of claim 1 wherein the initial support material is SBA-15.

10. The method of preparing an acidic catalyst of claim 1 wherein the initial support material is ZSM-5.

11. A method of preparing an acidic catalyst comprising:

a. heating a metal halide to produce a vapor phase metal halide;

b. contacting an initial support material with the vapor phase metal halide in a reaction vessel thereby causing a first chemical reaction and thereby producing an intermediate acidic catalyst;

c. wherein the initial support material is selected from an aluminum oxide based catalyst and a silicon oxide based catalyst;

d. wherein the vapor phase metal halide is selected from aluminum trichloride and aluminum tribromide;

e. contacting the intermediate acidic catalyst with between 0.1% and 20% gas phase HBr in an inert gas thereby causing a second chemical reaction and thereby producing an acidic catalyst product.

12. The method of preparing an acidic catalyst of claim 11 wherein the metal halide is aluminum trichloride and the initial support material is silica gel.

13. The method of preparing an acidic catalyst of claim 11 wherein the initial support material is MCM-41.

14. The method of preparing an acidic catalyst of claim 11 wherein the initial support material is SBA-15.

15. The method of preparing an acidic catalyst of claim 11 wherein the initial support material is ZSM-5.

16. A method of preparing an acidic catalyst comprising:

a. heating a metal halide to produce a vapor phase metal halide;

b. contacting an initial support material with the vapor phase metal halide in a reaction vessel thereby causing a first chemical reaction and thereby producing an intermediate acidic catalyst;

c. wherein the initial support material is selected from an aluminum oxide based catalyst and a silicon oxide based catalyst;

d. wherein the vapor phase metal halide is selected from aluminum trichloride and aluminum tribromide;

e. contacting the intermediate acidic catalyst with HBr thereby causing a second chemical reaction and thereby producing an acidic catalyst product;

f. wherein the HBr is gas phase HBr; and

g. wherein the heating of the metal halide to produce the vapor phase metal halide and the contacting the intermediate acidic catalyst with HBr are separate sequential steps.

17. The method of preparing an acidic catalyst of claim 16 wherein the metal halide is aluminum trichloride and the initial support material is silica gel.

18. The method of preparing an acidic catalyst of claim 16 wherein the initial support material is MCM-41.

19. The method of preparing an acidic catalyst of claim 16 wherein the initial support material is SBA-15.

20. The method of preparing an acidic catalyst of claim 16 wherein the initial support material is ZSM-5.

Assignments (1)
CONFIRMATORY LICENSE Recorded Nov 16, 2020
From: LOUISIANA STATE UNIVERSITY
To: NATIONAL SCIENCE FOUNDATION
Reel/Frame 054439/0108 →
Continuity (4)
Continuation 16403172 · May 3, 2019
Continuation 15867920 · Jan 11, 2018
Provisional Application 62488466 · Apr 21, 2017
Related Publication 20200197915A1 · Jun 25, 2020