IP Library Granted Patent US 8,900,417
Granted Patent B2
US 8,900,417 · App. 13/808,358 · Granted Dec 2, 2014

Purification method of 2,3,3,3-tetrafluoropropene

Inventors: Takehiro Chaki (Settsu, JP); Kazuhiro Takahashi (Settsu, JP)
Assignee: Daikin Industries, Ltd.
C07C17/386C01B7/196C07C17/38C07C17/383
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Quick Facts
Patent No.
US 8,900,417
App. No.
13/808,358
Granted
Dec 2, 2014
Kind
B2
Abstract

This invention provides a method for purifying HFO-1234yf by removing HF from a mixture of HFO-1234yf and HF under simple and economically advantageous conditions. According to the present invention, this is a purification method for 2,3,3,3-tetrafluoropropene, (1) the purification method comprising the step of subjecting a mixture comprising 2,3,3,3-tetrafluoropropene and hydrogen fluoride to extractive distillation in a distillation column A using an extractant, thereby obtaining a fraction I that contains 2,3,3,3-tetrafluoropropene and has a lower ratio of hydrogen fluoride to 2,3,3,3-tetrafluoropropene than that of the mixture, while obtaining a fraction II that contains hydrogen fluoride and has a lower ratio of 2,3,3,3-tetrafluoropropene to hydrogen fluoride than that of the mixture; (2) the extractant comprising at least one member selected from the group consisting of: (i) alcohols represented by ROH, wherein R is a C 1-5 alkyl group, (ii) ethers represented by ROR′, wherein R and R′ are the same or different, and each is a C 1-4 alkyl group, (iii) fluorinated alcohols represented by RfOH, wherein Rf is a C 1-3 fluoroalkyl group, (iv) ketones represented by RCOR′, wherein R and R′ are the same or different, and each is a C 1-4 alkyl group, (v) esters represented by RCOOR′, wherein R and R′ are the same or different, and each is a C 1-4 alkyl group, (vi) polyols represented by R(OH)n, wherein R is a C 1-4 alkyl group, and n is an integer of 2 to 3, and (vii) ethylene glycols represented by R 1 O(CH 2 CH 2 O) n R 2 , wherein R 1 and R 2 are the same or different, and each is hydrogen or a C 1-4 alkyl group, and n is an integer of 1 to 3.

Claims (29)

1. A method for purifying 2,3,3,3-tetrafluoropropene,

(1) the purification method comprising the step of subjecting a mixture comprising 2,3,3,3-tetrafluoropropene and hydrogen fluoride to extractive distillation in a distillation column A using an extractant, thereby obtaining a fraction I that contains 2,3,3,3-tetrafluoropropene and has a lower ratio of hydrogen fluoride to 2,3,3,3-tetrafluoropropene than the mixture, while obtaining a fraction II that contains hydrogen fluoride and has a lower ratio of 2,3,3,3-tetrafluoropropene to hydrogen fluoride than the mixture;

(2) the extractant comprising at least one member selected from the group consisting of:

(i) alcohols represented by ROH, wherein R is a C 1-5 alkyl group,

(ii) ethers represented by ROR′, wherein R and R′ are the same or different, and each is a C 1-4 alkyl group,

(iii) fluorinated alcohols represented by RfOH, wherein Rf is a C 1-3 fluoroalkyl group,

(iv) ketones represented by RCOR′, wherein R and R′ are the same or different, and each is a C 1-4 alkyl group,

(v) esters represented by RCOOR′, wherein R and R′ are the same or different, and each is a C 1-4 alkyl group,

(vi) polyols represented by R(OH) n , wherein R is a C 1-4 alkyl group, and n is an integer of 2 to 3, and

(vii) ethylene glycols represented by R 1 O(CH 2 CH 2 O) n R 2 , wherein R 1 and R 2 are the same or different, and each is hydrogen or a C 1-4 alkyl group, and n is an integer of 1 to 3.

2. The purification method according to claim 1 , wherein the extractant comprises at least one member selected from the group consisting of methanol, ethanol, propanol, butanol, isopropanol, 2-methoxyethanol, dimethyl ether, diethyl ether, diisopropyl ether, trifluoroethanol, pentafluoropropanol, tetrafluoropropanol, acetone, methyl acetate, ethyl acetate, propyl acetate, butyl acetate, 1,4-dioxane, 1,3,5-trioxane, diisopropyl ether, and bis(2-methoxymethyl)ether.

3. The purification method according to claim 1 , wherein the extractant has a boiling point higher than that of hydrogen fluoride, the fraction I is obtained from the top of the distillation column A, while the fraction II is obtained from the bottom of the distillation column A, and the method comprises the step of feeding the fraction II to a distillation column B in which the fraction II is distilled, thereby obtaining a fraction III that contains hydrogen fluoride and has a higher ratio of hydrogen fluoride than the fraction II from the top of the distillation column B, while obtaining a fraction IV that contains the extractant from the bottom of the distillation column B.

4. The purification method according to claim 3 , wherein the fraction IV is used as at least a part of the extractant used in the distillation column A.

5. The purification method according to claim 1 , wherein the extractant has a boiling point lower than hydrogen fluoride, the fraction I is obtained from the top of the distillation column A, while the fraction II is obtained from the bottom of the distillation column A, and the method comprises the step of feeding the fraction II to a distillation column B in which the fraction II is distilled, thereby obtaining a fraction III that contains hydrogen fluoride and has a higher ratio of hydrogen fluoride than the fraction II from the bottom of the distillation column B, while obtaining a fraction IV that contains the extractant from the top of the distillation column B.

6. The purification method according to claim 5 , wherein the fraction IV is used as at least a part of the extractant used in the distillation column A.

7. The purification method according to claim 1 , wherein the mixture comprises at least one member selected from the group consisting of 2-chloro-3,3,3-trifluoropropene, 2-chloro-1,1,1,2-tetrafluoropropane, 1,1,1,2,2-pentafluoropropane, 1,1,1,2,3-pentafluoropropane, E,Z-1,3,3,3-pentafluoropropene, 3,3,3-trifluoropropene, and 3,3,3-trifluoropropyne.

8. The purification method according to claim 2 , wherein the extractant has a boiling point higher than that of hydrogen fluoride, the fraction I is obtained from the top of the distillation column A, while the fraction II is obtained from the bottom of the distillation column A, and the method comprises the step of feeding the fraction II to a distillation column B in which the fraction II is distilled, thereby obtaining a fraction III that contains hydrogen fluoride and has a higher ratio of hydrogen fluoride than the fraction II from the top of the distillation column B, while obtaining a fraction IV that contains the extractant from the bottom of the distillation column B.

9. The purification method according to claim 8 , wherein the fraction IV is used as at least a part of the extractant used in the distillation column A.

10. The purification method according to claim 2 , wherein the extractant has a boiling point lower than hydrogen fluoride, the fraction I is obtained from the top of the distillation column A, while the fraction II is obtained from the bottom of the distillation column A, and the method comprises the step of feeding the fraction II to a distillation column B in which the fraction II is distilled, thereby obtaining a fraction III that contains hydrogen fluoride and has a higher ratio of hydrogen fluoride than the fraction II from the bottom of the distillation column B, while obtaining a fraction IV that contains the extractant from the top of the distillation column B.

11. The purification method according to claim 10 , wherein the fraction IV is used as at least a part of the extractant used in the distillation column A.

12. The purification method according to claim 2 , wherein the mixture comprises at least one member selected from the group consisting of 2-chloro-3,3,3-trifluoropropene, 2-chloro-1,1,1,2-tetrafluoropropane, 1,1,1,2,2-pentafluoropropane, 1,1,1,2,3-pentafluoropropane, E,Z-1,3,3,3-pentafluoropropene, 3,3,3-trifluoropropene, and 3,3,3-trifluoropropyne.

13. The purification method according to claim 3 , wherein the mixture comprises at least one member selected from the group consisting of 2-chloro-3,3,3-trifluoropropene, 2-chloro-1,1,1,2-tetrafluoropropane, 1,1,1,2,2-pentafluoropropane, 1,1,1,2,3-pentafluoropropane, E,Z-1,3,3,3-pentafluoropropene, 3,3,3-trifluoropropene, and 3,3,3-trifluoropropyne.

14. The purification method according to claim 4 , wherein the mixture comprises at least one member selected from the group consisting of 2-chloro-3,3,3-trifluoropropene, 2-chloro-1,1,1,2-tetrafluoropropane, 1,1,1,2,2-pentafluoropropane, 1,1,1,2,3-pentafluoropropane, E,Z-1,3,3,3-pentafluoropropene, 3,3,3-trifluoropropene, and 3,3,3-trifluoropropyne.

15. The purification method according to claim 5 , wherein the mixture comprises at least one member selected from the group consisting of 2-chloro-3,3,3-trifluoropropene, 2-chloro-1,1,1,2-tetrafluoropropane, 1,1,1,2,2-pentafluoropropane, 1,1,1,2,3-pentafluoropropane, E,Z-1,3,3,3-pentafluoropropene, 3,3,3-trifluoropropene, and 3,3,3-trifluoropropyne.

16. The purification method according to claim 6 , wherein the mixture comprises at least one member selected from the group consisting of 2-chloro-3,3,3-trifluoropropene, 2-chloro-1,1,1,2-tetrafluoropropane, 1,1,1,2,2-pentafluoropropane, 1,1,1,2,3-pentafluoropropane, E,Z-1,3,3,3-pentafluoropropene, 3,3,3-trifluoropropene, and 3,3,3-trifluoropropyne.

17. The purification method according to claim 8 , wherein the mixture comprises at least one member selected from the group consisting of 2-chloro-3,3,3-trifluoropropene, 2-chloro-1,1,1,2-tetrafluoropropane, 1,1,1,2,2-pentafluoropropane, 1,1,1,2,3-pentafluoropropane, E,Z-1,3,3,3-pentafluoropropene, 3,3,3-trifluoropropene, and 3,3,3-trifluoropropyne.

18. The purification method according to claim 9 , wherein the mixture comprises at least one member selected from the group consisting of 2-chloro-3,3,3-trifluoropropene, 2-chloro-1,1,1,2-tetrafluoropropane, 1,1,1,2,2-pentafluoropropane, 1,1,1,2,3-pentafluoropropane, E,Z-1,3,3,3-pentafluoropropene, 3,3,3-trifluoropropene, and 3,3,3-trifluoropropyne.

19. The purification method according to claim 10 , wherein the mixture comprises at least one member selected from the group consisting of 2-chloro-3,3,3-trifluoropropene, 2-chloro-1,1,1,2-tetrafluoropropane, 1,1,1,2,2-pentafluoropropane, 1,1,1,2,3-pentafluoropropane, E,Z-1,3,3,3-pentafluoropropene, 3,3,3-trifluoropropene, and 3,3,3-trifluoropropyne.

20. The purification method according to claim 11 , wherein the mixture comprises at least one member selected from the group consisting of 2-chloro-3,3,3-trifluoropropene, 2-chloro-1,1,1,2-tetrafluoropropane, 1,1,1,2,2-pentafluoropropane, 1,1,1,2,3-pentafluoropropane, E,Z-1,3,3,3-pentafluoropropene, 3,3,3-trifluoropropene, and 3,3,3-trifluoropropyne.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 4, 2013
From: CHAKI, TAKEHIRO; TAKAHASHI, KAZUHIRO
To: DAIKIN INDUSTRIES, LTD.
Reel/Frame 029569/0137 →
Continuity (2)
Provisional Application 61367050 · Jul 23, 2010
Related Publication 20130105296A1 · May 2, 2013