IP Library Granted Patent US 7,566,809
Granted Patent B2
US 7,566,809 · App. 11/753,970 · Granted Jul 28, 2009

Process for separation of a mixture comprising at least one hydrofluoroalkane

Assignee: Solvay S.A.
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Quick Facts
Patent No.
US 7,566,809
App. No.
11/753,970
Granted
Jul 28, 2009
Kind
B2
Abstract

Process for the separation of a mixture comprising at least one hydrofluoroalkane and hydrogen fluoride, according to which a hydrofluoroalkane/hydrogen fluoride mixture is reacted with at least one chlorinated or chlorofluorinated precursor of the hydrofluoroalkane. Process for the preparation of a hydrofluoroalkane comprising such a separation, in combination with a catalytic reaction stage. Azeotropic compositions.

Claims (20)

1. A process for the manufacture of 1,1,1,3,3-pentafluorobutane, which comprises reacting a chlorinated precursor with hydrogen fluoride to produce 1,1,1,3,3-pentafluorobutane and separating the 1,1,1,3,3-pentafluorobutane by using an azeotropic or pseudo-azeotropic composition which comprises 1.5 mol % to 27.5 mol % of 1,1,1,3,3-pentafluorobutane and 72.5 mol % to 98.5 mol % of hydrogen fluoride.

2. The process according to claim 1 , wherein the composition is used for the purification of 1,1,1,3,3-pentafluorobutane.

3. The process according to claim 1 , wherein the composition is used for separation of 1,1,1,3,3-pentafluorobutane and of hydrogen fluoride from a reaction mixture.

4. The process according to claim 1 , which comprises synthezising 1,1,1,3,3-pentafluorobutane by hydrofluorination of a chlorinated precursor.

5. The process according to claim 2 , which comprises synthezising 1,1,1,3,3-pentafluorobutane by hydrofluorination of a chlorinated precursor.

6. The process according to claim 3 , which comprises synthezising 1,1,1,3,3-pentatluorobutane by hydrofluorination of a chlorinated precursor.

7. The process according to claim 1 , wherein under a pressure of one bar the azeotropic or the pseudo-azeotropic composition comprises 1.5 mol % to 9 mol % of 1,1,1,3,3-pentafluorobutane and 91 mol % to 98.5 mol % of hydrogen fluoride.

8. The process according to claim 1 , wherein the azeotropic or the pseudo-azeotropic composition comprises 1.5 mol % to 9 mol % of 1,1,1,3,3-pentafluorobutane and 91 mol % to 98.5 mol % of hydrogen fluoride.

9. The process according to claim 1 , wherein the azeotropic or the pseudo-azeotropic composition comprises 15 mol % to 22 mol % of 1,1,1,3,3-pentafluorobutane and 78 mol % to 85 mol % of hydrogen fluoride.

10. The process according to claim 1 , wherein the azeotropic or the pseudo-azeotropic composition comprises 16 mol % to 25 mol % of 1,1,1,3,3-pentafluorobutane and 75 mol % to 84 mol % of hydrogen fluoride.

11. In a process for the manufacture of 1,1,1,3,3-pentafluorobutane wherein the improvement comprises separating impurities from 1,1,1,3,3-pentafluorobutane by using an azeotropic or pseudo-azeotropic composition which comprises 1.5 mol % to 27.5 mol % of 1,1,1,3,3-pentafluorobutane and 72.5 mol % to 98.5 mol % of hydrogen fluoride.

12. The process according to claim 11 , wherein the composition is used for the purification of 1,1,1,3,3-pentafluorobutane.

13. The process according to claim 11 , wherein the composition is used for separation of 1,1,1,3,3-pentafluorobutane and of hydrogen fluoride from a reaction mixture.

14. The process according to claim 11 , which comprises synthezising 1,1,1,3,3-pentafluorobutane by hydrofluorination of a chlorinated precursor.

15. The process according to claim 11 , wherein under a pressure of one bar the azeotropic or the pseudo-azeotropic composition comprises 1.5 mol % to 9 mol % of 1,1,1,3,3-pentafluorobutane and 91 mol % to 98.5 mol % of hydrogen fluoride.

16. The process according to claim 11 , wherein the azeotropic or the pseudo-azeotropic composition comprises 1.5 mol % to 9 mol % of 1,1,1,3,3-pentafluorobutane and 91 mol % to 98.5 mol % of hydrogen fluoride.

17. The process according to claim 11 , wherein the azeotropic or the pseudo-azeotropic composition comprises 15 mol % to 22 mol % of 1,1,1,3,3-pentafluorobutane and 78 mol % to 85 mol % of hydrogen fluoride.

18. The process according to claim 11 , wherein the azeotropic or the pseudo-azeotropic composition comprises 16 mol % to 25 mol % of 1,1,1,3,3-pentafluorobutane and 75 mol % to 84 mol % of hydrogen fluoride.

19. A process for the purification of 1,1,1,3,3-pentafluorobutane which comprises impurities which comprises separating the impurities which do not form an azeotrope with hydrogen fluoride or which have an azeotrope with hydrogen fluoride by using an azeotropic or pseudo-azeotropic composition which comprises 1.5 mol % to 27.5 mol % of 1,1,1,3,3-pentafluorobutane and 72.5 mol % to 98.5 mol % of hydrogen fluoride and said impurities exhibit a boiling point markedly different from said azeotropic or pseudo-azeotropic composition and to separate the 1,1,1,3,3-pentafluorobutane and hydrogen fluoride.

20. The process as claimed in claim 19 , wherein the separation of 1,1,1,3,3-pentafluorobutane and of hydrogen fluoride is from a reaction mixture obtained in a process for the synthesis of 1,1,1,3,3-pentafluorobutane by hydrofluorination of a chlorinated precursor.

Assignments (1)
JUDGMENT/LIEN/SECURITY INTEREST Recorded Dec 8, 2009
From: CENTRO DE INGENIERA GENETICA Y BIOTECNOLOGIA
To: JEREZ, NILO, MR.
Reel/Frame 023620/0190 →
Priority Claims (1)
BE 9800910 · Dec 18, 1998 · national
Continuity (4)
Division 1147630600 · Jun 28, 2006
Continuation 1028278500 · Oct 29, 2002
Division 0986836800
Related Publication 20080033219A1 · Feb 7, 2008