IP Library Granted Patent US 12,415,732
Granted Patent B2
US 12,415,732 · App. 18/632,743 · Granted Sep 16, 2025

Modified zeolites that include zirconium-containing organometallic moieties and methods for making such

Inventors: Robert Peter Hodgkins (Dhahran, SA); Omer Refa Koseoglu (Dhahran, SA); Jean-Marie Maurice Basset (Thuwal, SA); Kuo-Wei Huang (Thuwal, SA); Anissa Bendjeriou Sedjerari (Thuwal, SA); Manoj K. Gangwar (Thuwal, SA); Sathiyamoorthy Murugesan (Thuwal, SA)
Assignees: Saudi Arabian Oil Company; King Abdullah University of Science and Technology
C01B39/026B01J29/405C01B39/40B01J2229/186B01J2229/34C01P2002/82C01P2002/86C01P2004/62C01P2004/64C01P2006/16
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Quick Facts
Patent No.
US 12,415,732
App. No.
18/632,743
Granted
Sep 16, 2025
Kind
B2
Abstract

Disclosed herein are modified zeolites and methods for making modified zeolites. In one or more embodiments disclosed herein, a zeolite may include a microporous framework comprising a plurality of micropores having diameters of less than or equal to 2 nm. The microporous framework may include at least silicon atoms and oxygen atoms. The modified zeolite may further include organometallic moieties each bonded to bridging oxygen atoms. The organometallic moieties may include a zirconium atom. The zirconium atom may be bonded to a bridging oxygen atom, and the bridging oxygen atom may bridge the zirconium atom of the organometallic moiety and a silicon atom of the microporous framework.

Claims (20)

1. A method for making a modified zeolite, the method comprising:

reacting an organometallic chemical with a dehydroxylated zeolite, wherein the dehydroxylated zeolite comprises a microporous framework comprising a plurality of micropores having diameters of less than or equal to 2 nm, wherein the microporous framework comprises at least silicon atoms and oxygen atoms, and wherein the dehydroxylated zeolite comprises terminal isolated silanol functionalities comprising hydroxyl groups bonded to silicon atoms of the microporous framework;

wherein the reacting of the organometallic chemical with the dehydroxylated zeolite forms the modified zeolite comprising organometallic moieties each bonded to an oxygen atom of the modified zeolite, wherein the organometallic moiety comprises a portion of the organometallic chemical;

wherein the organometallic chemical comprises zirconium.

2. The method of claim 1 , wherein the modified zeolite comprises a plurality of mesopores having diameters of greater than 2 nm and less than or equal to 50 nm.

3. The method of claim 1 , wherein the average pore size of the modified zeolite is greater than 2 nm.

4. The method of claim 1 , further comprising dehydroxylating an initial zeolite to form the dehydroxylated zeolite, wherein the initial zeolite primarily comprises vicinal silanol functionalities, and wherein dehydroxylating the initial zeolite forms the terminal isolated silanol functionalities.

5. The method of claim 4 , wherein one or more of:

dehydroxylating the initial zeolite comprises heating the initial zeolite at a temperature of 650° C. to 1100° C.; and

dehydroxylating the initial zeolite is under reduced pressure.

6. The method of claim 1 , wherein the microporous framework further comprises aluminum atoms.

7. The method of claim 1 , wherein the average pore size of the dehydroxylated zeolite is greater than the size of the organometallic chemical.

8. The method of claim 1 , wherein the organometallic chemical comprises ZrR 1 R 2 R 3 R 4 , wherein:

R 1 is chosen from any of an alkyl group, a hydride group, a hydroxyl group, an alkoxy group, an aryloxy group, an allyl group, a cyclopentadienyl group, an amino group, an amido group, an imido group, a nitrido group, a carbene group, a carbyne group, a halide group, a benzyl group, a phenyl group, or an oxo group;

R 2 is chosen from any of an alkyl group, a hydride group, a hydroxyl group, an alkoxy group, an aryloxy group, an allyl group, a cyclopentadienyl group, an amino group, an amido group, an imido group, a nitrido group, a carbene group, a carbyne group, a halide group, a benzyl group, a phenyl group, or an oxo group;

R 3 is chosen from any of an alkyl group, a hydride group, a hydroxyl group, an alkoxy group, an aryloxy group, an allyl group, a cyclopentadienyl group, an amino group, an amido group, an imido group, a nitrido group, a carbene group, a carbyne group, a halide group, a benzyl group, a phenyl group, or an oxo group; and

R 4 is chosen from any of an alkyl group, a hydride group, a hydroxyl group, an alkoxy group, an aryloxy group, an allyl group, a cyclopentadienyl group, an amino group, an amido group, an imido group, a nitrido group, a carbene group, a carbyne group, a halide group, a benzyl group, a phenyl group, or an oxo group.

9. The method of claim 1 , wherein the organometallic chemical comprises tetrakis(neopentyl)zirconium.

10. The method of claim 1 , wherein the organometallic moieties of the modified zeolite comprise zirconium.

11. The method of claim 1 , wherein the organometallic moieties of the modified zeolite comprise tris(neopentyl)zirconium.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 11, 2024
From: HODGKINS, ROBERT PETER; KOSEOGLU, OMER REFA
To: SAUDI ARABIAN OIL COMPANY
Reel/Frame 067080/0986 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 11, 2024
From: BASSETT, JEAN-MARIE MAURICE; HUANG, KUO-WEI; BENDJERIOU SEDJERARI, ANISSA; GANGWAR, MANOJ K.; MURUGESAN, SATHIYAMOORTHY
To: KING ABDULLAH UNIVERSITY OF SCIENCE AND TECHNOLOGY
Reel/Frame 067081/0125 →
Continuity (2)
Division 17230505 · Apr 14, 2021
Related Publication 20240286911A1 · Aug 29, 2024
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