IP Library Granted Patent US 6,984,606
Granted Patent B2
US 6,984,606 · App. 10/782,172 · Granted Jan 10, 2006

Epoxidation catalyst

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Quick Facts
Patent No.
US 6,984,606
App. No.
10/782,172
Granted
Jan 10, 2006
Kind
B2
Abstract

Noble metal-containing titanium zeolite catalysts are prepared by reacting a titanium compound, a silicon source, a templating agent, and a noble metal source at a temperature and for a time sufficient to form a molecular sieve. The catalyst is useful in olefin epoxidation with oxygen and hydrogen.

Claims (20)

1. A process for producing a noble metal-containing titanium zeolite, which comprises reacting a titanium compound, a silicon source, a templating agent, and a noble metal source at a temperature and for a time sufficient to form a molecular sieve, wherein the noble metal source comprises one or more noble metals selected from the group consisting of palladium, platinum, and gold.

2. The process of claim 1 wherein the titanium compound is selected from the group consisting of titanium halides, titanium alkoxides, and mixtures thereof.

3. The process of claim 2 wherein the titanium compound is a titanium alkoxide selected from the group consisting of titanium tetraethoxide, titanium tetraisopropoxide, titanium tetrabutoxide, and mixtures thereof.

4. The process of claim 1 wherein the silicon source is selected from the group consisting of colloidal silica, fumed silica, silicon alkoxides, and mixtures thereof.

5. The process of claim 4 wherein the silicon source is a silicon alkoxide selected from the group consisting of tetraethylorthosilicate, tetramethylorthosilicate, and mixtures thereof.

6. The process of claim 1 wherein the templating agent is selected from the group consisting of tetraalkylammonium hydroxide, tetraalkylammonium halides, and mixtures thereof.

7. The process of claim 6 wherein the templating agent is selected from the group consisting of tetrapropylammonium hydroxide, tetrapropylammonium halides, and mixtures thereof.

8. The process of claim 1 wherein the noble metal source comprises palladium.

9. The process of claim 1 wherein the noble metal-containing titanium zeolite comprises a titanium silicalite is selected from the group consisting of TS-1 and TS-2.

10. A epoxidation process comprising reacting an olefin, hydrogen, and oxygen in the presence of a noble metal-containing titanium zeolite, wherein the noble metal-containing titanium zeolite is produced by reacting a titanium compound, a silicon source, a templating agent, and a noble metal source at a temperature and for a time sufficient to form a molecular sieve, and wherein the noble metal source comprises one or more noble metals selected from the group consisting of palladium, platinum, and gold.

11. The process of claim 10 wherein the titanium compound is selected from the group consisting of titanium halides, titanium alkoxides, and mixtures thereof.

12. The process of claim 11 wherein the titanium compound is a titanium alkoxide selected from the group consisting of titanium tetraethoxide, titanium tetraisopropoxide, titanium tetrabutoxide, and mixtures thereof.

13. The process of claim 10 wherein the silicon source is selected from the group consisting of colloidal silica, fumed silica, silicon alkoxides, and mixtures thereof.

14. The process of claim 13 wherein the silicon source is a silicon alkoxide selected from the group consisting of tetraethylorthosilicate, tetramethylorthosilicate, and mixtures thereof.

15. The process of claim 10 wherein the templating agent is selected from the group consisting of tetraalkylammonium hydroxide, tetraalkylammonium halides, and mixtures thereof.

16. The process of claim 15 wherein the templating agent is selected from the group consisting of tetrapropylammonium hydroxide, tetrapropylammonium halides, and mixtures thereof.

17. The process of claim 10 wherein the noble metal source comprises palladium.

18. The process of claim 10 wherein the olefin is a C 2 –C 6 olefin.

19. The process of claim 10 wherein the olefin is propylene and propylene oxide is formed.

20. The process of claim 10 wherein reaction of olefin, hydrogen, and oxygen is performed in a reaction solvent selected from the group consisting of methanol, ethanol, isopropanol, tert-butanol, water, and mixtures thereof.

Assignments (21)
RELEASE OF SECURITY INTEREST Recorded Jan 23, 2014
From: DEUTSCHE BANK TRUST COMPANY AMERICAS
To: LYONDELL CHEMICAL TECHNOLOGY, L.P.
Reel/Frame 032123/0799 →
RELEASE OF SECURITY INTEREST Recorded Jan 23, 2014
From: CITIBANK, N.A.
To: LYONDELL CHEMICAL TECHNOLOGY, L.P.
Reel/Frame 032125/0296 →
RELEASE OF SECURITY INTEREST Recorded Jan 23, 2014
From: WELLS FARGO BANK, NATIONAL ASSOCIATION
To: LYONDELL CHEMICAL TECHNOLOGY, L.P.
Reel/Frame 032137/0156 →
APPOINTMENT OF SUCCESSOR ADMINISTRATIVE AGENT Recorded Jan 23, 2014
From: UBS AG, STAMFORD BRANCH
To: BANK OF AMERICA, N.A.
Reel/Frame 032137/0639 →
RELEASE OF SECURITY INTEREST Recorded Jan 23, 2014
From: BANK OF AMERICA, N.A.
To: LYONDELL CHEMICAL TECHNOLOGY, L.P.
Reel/Frame 032138/0134 →
SECURITY AGREEMENT Recorded May 19, 2010
From: LYONDELL CHEMICAL TECHNOLOGY, L.P.
To: WELLS FARGO BANK, NATIONAL ASSOCIATION, AS COLLATERAL AGENT
Reel/Frame 024402/0681 →
SECURITY AGREEMENT Recorded May 18, 2010
From: LYONDELL CHEMICAL TECHNOLOGY, L.P.
To: CITIBANK, N.A., AS ADMINISTRATIVE AGENT
Reel/Frame 024397/0818 →
SECURITY AGREEMENT Recorded May 7, 2010
From: LYONDELL CHEMICAL TECHNOLOGY, L.P.
To: UBS AG, STAMFORD BRANCH, AS COLLATERAL AGENT
Reel/Frame 024342/0801 →
SECURITY AGREEMENT Recorded May 6, 2010
From: LYONDELL CHEMICAL TECHNOLOGY, L.P.
To: DEUTSCHE BANK TRUST COMPANY AMERICAS, AS COLLATERAL AGENT
Reel/Frame 024342/0421 →
RELEASE OF SECURITY INTEREST Recorded May 5, 2010
From: CITIBANK, N.A., AS COLLATERAL AGENT
To: LYONDELL CHEMICAL TECHNOLOGY, L.P.; EQUISTAR CHEMICALS, LP
Reel/Frame 024337/0856 →
RELEASE OF SECURITY INTEREST Recorded May 5, 2010
From: CITIBANK, N.A., AS COLLATERAL AGENT
To: LYONDELL CHEMICAL TECHNOLOGY, L.P.; EQUISTAR CHEMICALS, LP
Reel/Frame 024337/0705 →
RELEASE OF SECURITY INTEREST Recorded May 5, 2010
From: UBS AG, STAMFORD BRANCH, AS COLLATERAL AGENT
To: LYONDELL CHEMICAL TECHNOLOGY, LP
Reel/Frame 024337/0285 →
RELEASE OF SECURITY INTEREST Recorded May 5, 2010
From: CITIBANK, N.A., AS COLLATERAL AGENT
To: LYONDELL CHEMICAL TECHNOLOGY, LP
Reel/Frame 024337/0020 →
SECURITY AGREEMENT Recorded Oct 30, 2009
From: LYONDELL CHEMICAL TECHNOLOGY, L.P.
To: UBS AG, STAMFORD BRANCH, AS COLLATERAL AGENT
Reel/Frame 023449/0138 →
SECURITY AGREEMENT Recorded Apr 9, 2009
From: LYONDELL CHEMICAL TECHNOLOGY, L.P.
To: CITIBANK, N.A., AS ADMINISTRATIVE AGENT AND COLLATERAL AGENT
Reel/Frame 022708/0830 →
SECURITY AGREEMENT Recorded Aug 4, 2008
From: BASELL POLYOLEFINE GMBH; ARCO CHEMICAL TECHNOLOGY L.P.; ARCO CHEMICAL TECHNOLOGY, INC.; ATLANTIC RICHFIELD COMPANY; BASELL NORTH AMERICA, INC.; BASELL POLYOLEFIN GMBH; LYONDELL CHEMICAL COMPANY; EQUISTAR CHEMICALS, L.P.
To: CITIBANK, N.A., AS COLLATERAL AGENT
Reel/Frame 021354/0708 →
GRANT OF SECURITY INTEREST IN UNITED STATES PATENTS AND PATENT APPLICATIONS Recorded Mar 26, 2008
From: BASELL POLYOLEFINE GMBH; ARCO CHEMICAL TECHNOLOGY L.P.; ARCO CHEMICAL TECHNOLOGY, INC.; ATLANTIC RICHFIELD COMPANY; BASELL NORTH AMERICA, INC.; EQUISTAR CHEMICALS. LP.; LYONDELL CHEMICAL COMPANY; LYONDELL CHEMICAL TECHNOLOGY, L.P.; LYONDELL PETROCHEMICAL COMPANY; NATIONAL DISTILLERS AND CHEMICAL CORPORATION; OCCIDENTAL CHEMICAL CORPORATION; OLIN CORPORATION; QUANTUM CHEMICAL CORPORATION; BASELL POLYOLEFIN GMBH
To: CITIBANK, N.A., AS COLLATERAL AGENT
Reel/Frame 020704/0562 →
RELEASE OF LYONDELL CHEMICAL TECHNOLOGY, L.P. PATENT SECURITY AGREEMENT Recorded Mar 20, 2008
From: JPMORGAN CHASE BANK, N.A.
To: LYONDELL CHEMICAL TECHNOLOGY, L.P.
Reel/Frame 020679/0063 →
SECURITY AGREEMENT Recorded Sep 15, 2006
From: LYONDELL CHEMICAL TECHNOLOGY, L.P.
To: JPMORGAN CHASE BANK N.A., AS ADMINISTRATIVE AGENT
Reel/Frame 018260/0306 →
CHANGE OF NAME Recorded Jun 27, 2005
From: ARCO CHEMICAL TECHNOLOGY, L.P.
To: LYONDELL CHEMICAL TECHNOLOGY, L.P.
Reel/Frame 016206/0001 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 19, 2004
From: DESSAU, RALPH M.
To: ARCO CHEMICAL TECHNOLOGY, L.P.
Reel/Frame 015010/0135 →