IP Library Granted Patent US 9,187,392
Granted Patent B2
US 9,187,392 · App. 12/009,212 · Granted Nov 17, 2015

Production of propylene glycol monoalkyl ether

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Quick Facts
Patent No.
US 9,187,392
App. No.
12/009,212
Granted
Nov 17, 2015
Kind
B2
Abstract

The invention is a process for producing a propylene glycol monoalkyl ether which comprises first reacting propylene oxide and an alcohol in the presence of an alkali or alkaline earth metal alkoxide catalyst to produce an alkoxylation mixture comprising propylene glycol monoalkyl ether; distilling the alkoxylation mixture to produce a first overhead stream comprising propylene oxide and alcohol and a first bottoms stream comprising propylene glycol monoalkyl ether; and then distilling the first bottoms stream to produce purified propylene glycol monoalkyl ether as a second overhead stream. The reaction and/or one or more of the distillation steps occur in the presence of an alkali metal borohydride. The process produces propylene glycol monoalkyl ether with low UV absorbance and reduced carbonyl impurities.

Claims (30)

1. A process for producing a propylene glycol monoalkyl ether which comprises:

(a) reacting propylene oxide and an alcohol in the presence of an alkali or alkaline earth metal alkoxide catalyst to produce an alkoxylation mixture comprising propylene glycol monoalkyl ether and a component having a carbonyl functional group;

(b) distilling the alkoxylation mixture at a temperature of from about 50° C. to about 200° C. and a pressure of from about 1 psig to about 150 psig to produce a first overhead stream comprising propylene oxide and the alcohol and a first bottoms stream comprising propylene glycol monoalkyl ether; and

(c) distilling the first bottoms stream to produce purified propylene glycol monoalkyl ether as a second overhead stream,

wherein the reaction and/or one or more of the distillation steps occur in the presence of 0.05 to 1000 ppm, based upon the total weight of the alkoxylation mixture, of an alkali metal borohydride, and

wherein the alkali metal borohydride reduces the concentration of the component having a carbonyl functional group.

2. The process of claim 1 wherein the alcohol is a C 1 -C 4 alcohol.

3. The process of claim 1 wherein the alcohol is selected from the group consisting of methanol, 1-propanol, 1-butanol, and tert-butanol.

4. The process of claim 1 wherein the alkali or alkaline earth metal alkoxide catalyst is an alkali metal alkoxide.

5. The process of claim 4 wherein the alkali metal alkoxide catalyst is a potassium alkoxide or a sodium alkoxide.

6. The process of claim 5 wherein the potassium alkoxide is selected from the group consisting of potassium methoxide, potassium n-propoxide, potassium n-butoxide, and potassium t-butoxide.

7. The process of claim 5 wherein the sodium alkoxide is selected from the group consisting of sodium methoxide, sodium n-propoxide, sodium n-butoxide, and sodium t-butoxide.

8. The process of claim 1 wherein the alkali metal borohydride is sodium borohydride.

9. The process of claim 1 wherein the first overhead stream is recycled back to the reaction step (a).

10. The process of claim 1 wherein the propylene glycol monoalkyl ether is propylene glycol monomethyl ether.

11. The process of claim 1 wherein the alkali metal borohydride is added into the alkoxylation mixture prior to distillation step (b).

12. The process of claim 1 wherein the alkali metal borohydride is added into the first bottoms stream prior to distillation step (c).

13. The process of claim 1 wherein the purified propylene glycol monoalkyl ether has a UV absorbance, at 245 nm, of 1 or less.

14. A process for producing a propylene glycol monomethyl ether which comprises:

(a) reacting propylene oxide and methanol in the presence of an alkali metal methoxide catalyst to produce an alkoxylation mixture comprising propylene glycol monomethyl ether and a component having a carbonyl functional group;

(b) distilling the alkoxylation mixture at a temperature of from about 50° C. to about 200° C. and a pressure of from about 1 psiq to about 150 psiq to produce a first overhead stream comprising propylene oxide and methanol and a first bottoms stream comprising propylene glycol monomethyl ether; and

(c) distilling the first bottoms stream to produce purified propylene glycol monomethyl ether as a second overhead stream,

wherein the reaction and/or one or more of the distillation steps occur in the presence of 0.05 to 1000 ppm, based upon the total weight of the alkoxylation mixture, of sodium borohydride, and

wherein the sodium borohydride reduces the concentration of the component having a carbonyl functional group.

15. The process of claim 14 wherein the alkali metal methoxide catalyst is potassium methoxide.

16. The process of claim 14 wherein the alkali metal methoxide catalyst is sodium methoxide.

17. The process of claim 14 wherein the first overhead stream is recycled back to the reaction step (a).

18. The process of claim 14 wherein the sodium borohydride is added into the alkoxylation mixture prior to distillation step (b).

19. The process of claim 14 wherein the sodium borohydride is added into the first bottoms stream prior to distillation step (c).

20. The process of claim 14 wherein the purified propylene glycol monomethyl ether has a UV absorbance, at 245 nm, of 1 or less.

Assignments (14)
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: 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 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 17, 2008
From: LI, XIANGMIN; CANDELA, LAWRENCE M.; LIEPA, MARK A.
To: LYONDELL CHEMICAL TECHNOLOGY, L.P.
Reel/Frame 020443/0983 →