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

Patent metadata

Field	Value
Publication number	US-11565942-B2
Application number	US-202117230476-A
Country	US
Kind code	B2
Filing date	Apr 14, 2021
Priority date	Apr 14, 2021
Publication date	Jan 31, 2023
Grant date	Jan 31, 2023

Abstract

Disclosed herein are modified zeolites and methods for making modified zeolites. In one or more embodiments disclosed herein, a modified zeolite may include a microporous framework including 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 platinum atom. The platinum atom may be bonded to a bridging oxygen atom, and the bridging oxygen atom may bridge the platinum atom of the organometallic moiety and a silicon atom of the microporous framework.

First claim

The invention claimed is:

1. A modified zeolite comprising:
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
organometallic moieties each bonded to bridging oxygen atoms, wherein the organometallic moieties comprise a platinum atom, wherein the platinum atom is bonded to a bridging oxygen atom, and wherein the bridging oxygen atom bridges the platinum atom of the organometallic moiety and a silicon atom of the microporous framework.

2. The modified zeolite of claim 1 , further comprising a plurality of mesopores having diameters of greater than 2 nm and less than or equal to 50 nm.

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

4. The modified zeolite of claim 1 , wherein the organometallic moieties comprise platinum coordinated with one or more ligands, wherein the ligands comprise any of an alkyl group, an aryl group, a dienyl group, a pyridyl group, a cyclooctadienyl group, a cyclopentadienyl group, a quinolinyl group, a halogen group, or a sulfide group.

5. The modified zeolite of claim 1 , wherein the organometallic moieties comprise (1,5-cyclooctadiene)(methyl)platinum(II).

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

7. The modified zeolite of claim 1 , wherein the modified zeolite is a ZSM-5 zeolite.

8. The modified zeolite of claim 1 , wherein the modified zeolite comprises particles of from 25 nm to 900 nm in size.

9. 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 isolated terminal 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 the 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 organometallic moieties each bonded to bridging oxygen atoms, wherein the organometallic moieties comprise a platinum atom, wherein the platinum atom is bonded to a bridging oxygen atom, and wherein the bridging oxygen atom bridges the platinum atom of the organometallic moiety and a silicon atom of the microporous framework, wherein the organometallic moiety comprises a portion of the organometallic chemical;
wherein the organometallic chemical comprises platinum.

10. The method of claim 9 , wherein the modified zeolite comprises a plurality of mesopores having diameters of greater than 2 nm and less than or equal to 50 nm.

11. The method of claim 9 , wherein the average pore size of the modified zeolite is greater than 2 nm.

12. The method of claim 9 , 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 isolated terminal silanol functionalities.

13. The method of claim 12 , 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.

14. The method of claim 9 , wherein the microporous framework further comprises aluminum atoms.

15. The method of claim 9 , wherein the organometallic chemical comprises platinum coordinated with one or more ligands, wherein the ligands comprise any of an alkyl group, an aryl group, a dienyl group, a pyridine group, a cyclooctadienyl group, a cyclopentadienyl group, a quinolone group, a halogen group, or a sulfide group.

16. The method of claim 9 , wherein the organometallic chemical comprises (1,5-cyclooctadiene)(dimethyl)platinum(II).

17. The method of claim 9 , wherein the organometallic moieties of the modified zeolite comprise platinum coordinated with one or more ligands, wherein the ligands comprise any of a pyridine group, a cyclooctadienyl group, a cyclopentadienyl group, a quinolone group, a halogen group, or a sulfide group.

18. The method of claim 9 , wherein the organometallic moieties of the modified zeolite comprise (1,5-cyclooctadiene)methylplatinum(II).

19. The method of claim 9 , wherein the average pore size of the dehydroxylated zeolite is greater than the size of the organometallic chemical.

Assignees

• Saudi Arabian Oil Co
• Univ King Abdullah Sci & Tech

Inventors

• Hodgkins Robert Peter
• Koseoglu Omer Refa
• Basset Jean-Marie Maurice
• Huang Kuo-Wei
• Sedjerari Anissa Bendjeriou
• Gangwar Manoj K
• Murugesan Sathiyamoorthy

Classifications

• B01J37/0203

  the impregnation liquid containing organic compounds · CPC title

• B01J35/1061

  Operations & Transport · mapped topic

• C01B39/026 Primary

  After-treatment · CPC title

• B01J37/16

  Reducing · CPC title

• B01J35/1057

  Operations & Transport · mapped topic