IP Library Granted Patent US 8,592,630
Granted Patent B2
US 8,592,630 · App. 13/627,024 · Granted Nov 26, 2013

Processes for separating components in alkyl perfluoroalkene ether production

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Quick Facts
Patent No.
US 8,592,630
App. No.
13/627,024
Granted
Nov 26, 2013
Kind
B2
Abstract

Disclosed are processes for reacting a perfluorinated olefin with an alcohol, an alkali metal hydroxide, and water in the presence of a phase transfer catalyst to form a reaction product mixture that separates into an aqueous phase and an organic phase. Alcohol may be present in an effective amount sufficient to form a third phase comprising at least 50% of the phase transfer catalyst. The third phase can be separated from the organic phase. Also disclosed are methods for recovering and recycling the phase transfer catalyst used in the reaction.

Claims (38)

1. A process comprising:

a. contacting a perfluorinated olefin with an alcohol, an alkali metal hydroxide, and water in the presence of a phase transfer catalyst for a period of time to produce a reaction product mixture that separates into an aqueous phase and an organic phase, wherein the alcohol is present in an effective amount sufficient to form a third phase comprising at least 50% of the phase transfer catalyst; and

b. separating the third phase from the organic phase.

2. The process of claim 1 , wherein the perfluorinated olefin is perfluoro-3-heptene, pefluoro-2-heptene, perfluoro-2-hexene, perfluoro-3-hexene, perfluoro-2-pentene, or perfluoro-2-octene.

3. The process of claim 1 , wherein the phase transfer catalyst is chosen from onium salts and derivatives and mixtures thereof.

4. The process of claim 3 , wherein the phase transfer catalyst is chosen from quaternary ammonium salts and quaternary phosphonium salts.

5. The process of claim 3 , wherein said phase transfer catalyst is methyltrioctylammonium chloride and methyltridecylammonium chloride.

6. The process of claim 1 , wherein said alcohol is chosen from methanol and ethanol.

7. The process of claim 1 , wherein the said alcohol is present in an amount with respect to the perfluorinated olefin initially present ranging from about 1.1 to 1.5 times the stoichiometric amount.

8. The process of claim 1 , wherein said alkali metal hydroxide is sodium hydroxide or potassium hydroxide.

9. The process of claim 1 , wherein the process is a continuous process.

10. The process of claim 9 , wherein separating the third phase from the organic phase comprises separating the third phase from the organic phase in a continuous decanter.

11. The process of claim 1 , wherein separating the third phase from the organic phase comprises separating the aqueous phase with the third phase.

12. A process comprising:

a. contacting a perfluorinated olefin with an alcohol, an alkali metal hydroxide, and water in the presence of a phase transfer catalyst for a period of time to produce a reaction product mixture that is separable into an aqueous phase and an organic phase;

b. adding an additional amount of alcohol to the reaction product mixture, wherein the additional amount of alcohol forms a third phase comprising at least 50% of the phase transfer catalyst initially present.

13. A continuous process comprising:

a. feeding a reactant stream comprising a perfluorinated olefin, an alcohol, an alkali metal hydroxide, water, and a phase transfer catalyst to a reactor to produce a reaction product mixture;

b. transferring the reaction product mixture from the reactor to a separator;

c. adding an additional amount of alcohol to the reaction product mixture before the reaction product mixture enters the separator, wherein the additional amount of alcohol is added in an amount sufficient to prevent the formation of a rag layer during separation; and

d. separating an organic phase of the reaction product mixture from the remainder of the reaction product mixture in a continuous decanter, wherein the remainder of the reaction product mixture comprises an aqueous phase.

14. The process of claim 13 , wherein the organic phase comprises a heterogeneous azeotrope comprising fluorinated ethers and water, and the process further comprises drying the organic phase by distilling the heterogeneous azeotrope to remove the water.

15. The process of claim 14 , wherein distilling the heterogeneous azeotrope comprises separating perfluorinated olefin and water from an intermediate mixture in a first continuous distillation apparatus, and further separating the intermediate mixture into byproducts and saturated ethers in a second continuous distillation apparatus.

16. The process of claim 13 , wherein the additional amount of alcohol added to the reaction product mixture is added in an amount sufficient to form a third phase comprising at least 50% of the phase transfer catalyst in the reactant stream.

17. The process of claim 16 , wherein the additional amount of alcohol added to the product mixture is about 10% to about 50% of the amount of alcohol in the reactant stream.

18. The process of claim 16 , wherein the remainder of the reaction product mixture that is separated from the organic phase further comprises the third phase.

19. The process of claim 18 , further comprising separating the aqueous phase from the third phase.

20. The process of claim 18 , further comprising recovering the phase transfer catalyst in the third phase.

21. The process of claim 13 , wherein the perfluorinated olefin is chosen from perfluoro-3-heptene, pefluoro-2-heptene, perfluoro-2-hexene, perfluoro-3-hexene, perfluoro-2-pentene, and perfluoro-2-octene.

22. The process of claim 13 , wherein the alcohol is chosen from methanol and ethanol.

23. The process of claim 13 , wherein the phase transfer catalyst is chosen from onium salts and derivatives and mixtures thereof.

24. The process of claim 23 , wherein the phase transfer catalyst is chosen from quaternary ammonium salts and quaternary phosphonium salts.

25. The process of claim 24 , wherein the phase transfer catalyst comprises methyltrioctylammonium chloride and methyltridecylammonium chloride.

26. A process comprising:

a. contacting a perfluorinated olefin with an alcohol, an alkali metal hydroxide, and water in the presence of a phase transfer catalyst for a period of time to produce a reaction product mixture that is separable into an organic phase and an aqueous phase;

b. adding an additional amount of alcohol to the reaction product mixture, wherein the additional amount of alcohol forms a third phase comprising at least 50% of the phase transfer catalyst initially present;

c. separating the third phase from the organic phase and the aqueous phase; and

d. recovering the phase transfer catalyst from the third phase.

Assignments (5)
RELEASE OF SECURITY INTEREST Recorded Apr 4, 2018
From: JPMORGAN CHASE BANK, N.A., AS ADMINISTRATIVE AGENT
To: THE CHEMOURS COMPANY FC, LLC
Reel/Frame 045845/0913 →
SECURITY INTEREST Recorded Apr 4, 2018
From: THE CHEMOURS COMPANY FC, LLC
To: JPMORGAN CHASE BANK, N.A., AS ADMINISTRATIVE AGENT
Reel/Frame 045846/0011 →
SECURITY AGREEMENT Recorded Jun 10, 2015
From: THE CHEMOURS COMPANY FC LLC; THE CHEMOURS COMPANY TT, LLC
To: JPMORGAN CHASE BANK, N.A.
Reel/Frame 035839/0675 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 15, 2015
From: E. I. DU PONT DE NEMOURS AND COMPANY
To: THE CHEMOURS COMPANY FC, LLC
Reel/Frame 035432/0023 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 19, 2012
From: LOUSENBERG, ROBERT D.
To: E. I. DU PONT DE NEMOURS AND COMPANY
Reel/Frame 029156/0768 →