IP Library Granted Patent US 8,969,404
Granted Patent B2
US 8,969,404 · App. 13/758,080 · Granted Mar 3, 2015

Purifying crude furan 2,5-dicarboxylic acid by hydrogenation

Inventors: Mesfin Ejerssa Janka (Kingsport, TN); Charles Edwan Sumner, Jr. (Kingsport, TN); Shane Kipley Kirk (Church Hill, TN); Ashfaq Shahanawaz Shaikh (Kingsport, TN); Kenny Randolph Parker (Afton, TN)
Assignee: Eastman Chemical Company
C07D307/68
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Quick Facts
Patent No.
US 8,969,404
App. No.
13/758,080
Granted
Mar 3, 2015
Kind
B2
Abstract

A process for purifying a crude furan 2,5-dicarboxylic acid composition (cFDCA) by hydrogenation of a FDCA composition dissolved in a hydrogenation solvent such as water, and hydrogenating under mild conditions, such as at a temperature within a range of 130° C. to 225° C. by contacting the solvated FDCA composition with hydrogen in the presence of a hydrogenation catalyst under a hydrogen partial pressure within a range of 10 psi to 900 psi. A product FDCA composition is produced having a low amount of tetrahydrofuran dicarboxylic acid, a low b*, and a low amount of 5-formyl furan-2-carboxylic acid (FFCA).

Claims (43)

1. A process for purifying a crude furan 2,5-dicarboxylic acid composition (cFDCA) comprising:

a) providing a cFDCA composition comprising furan 2,5-dicarboxylic acid (FDCA) solids, 5-formyl furan-2-carboxylic acid (FFCA), and a oxidation solvent composition;

b) combining a hydrogenation solvent composition with said FDCA solids and dissolving at least a portion of the FDCA solids to thereby produce a solvated FDCA (sFDCA) composition comprising dissolved FDCA, the hydrogenation solvent composition, and FFCA;

c) in a hydrogenation reaction zone, hydrogenating the sFDCA at a temperature within a range of 130° C. to 225° C. by contacting the sFDCA composition with hydrogen in the presence of a hydrogenation catalyst to thereby hydrogenate FFCA and produce a furan 2,5-dicarboxylic acid composition (hFDCA) comprising a hydrogenated FFCA species, dissolved FDCA, and said hydrogenation solvent; and

e) separating at least a portion of the dissolved FDCA from the hFDCA composition to obtain a product FDCA (pFDCA) composition.

2. The process of claim 1 , wherein the cFDCA composition comprises at least 15 wt. % solids based on the weight of the cFDCA composition, wherein at least 85 wt. % of the solids is FDCA based on the weight of the solids; and FFCA.

3. The process of claim 2 , wherein the cFDCA composition comprises at least 28 wt. % solids based on the weight of the cFDCA composition, wherein at least 90 wt. % of the solids is FDCA based on the weight of the solids; and at least 0.2 wt. % FFCA.

4. The process of claim 2 , wherein the cFDCA composition comprises 2,5 diformylfuran in an amount of 0 wt % to about 0.2 wt %; levulinic acid in an amount ranging from 0 wt % to 0.5 wt %; succinic acid in an amount ranging from 0 wt % to 0.5 wt %; acetoxyacetic acid in an amount ranging from 0 wt % to 0.5 wt %, and a cumulative amount of by-products other than FFCA present in an amount ranging from greater than 0 wt. % and up to 20 wt. %, in each case based on the weight of cFDCA composition.

5. The process of claim 2 , wherein the cFDCA composition has a b* of at least 5.

6. The process of claim 1 , wherein the amount of FFCA by weight present in the cFDCA composition relative to FFCA present in the pFDCA is reduced by a factor of at least 100×.

7. The process of claim 6 , wherein the reduction of FFCA is by a factor of at least 500×.

8. The process of claim 1 , wherein the cFDCA composition is fed to an evaporator to remove at least a portion of the oxidation solvent from cFDCA composition to produce a concentrated slurry.

9. The process of claim 8 , wherein the concentrated slurry is fed to a solid/liquid separation zone to remove at least a portion of the oxidation solvent as a mother liquor to produce a wet cake, and said wet cake is washed to produce a washed cFDCA cake.

10. The process of claim 9 , wherein the washed cFDCA cake is fed to a dissolution zone for dissolving the washed cFDCA cake in a hydrogenation solvent composition.

11. The process of claim 1 , wherein the cFDCA composition is fed to a solid/liquid separation zone to separate the oxidation solvent from the cFDCA composition.

12. The process of claim 11 , wherein the FDCA solids are, after or simultaneous with separation of the oxidation solvent, combined with a hydrogenation solvent to dissolve at least 98% of the FDCA solids and thereby produce a solvated FDCA composition.

13. The process of claim 1 , wherein the FDCA solids in step b are dissolved in the hydrogenation solvent at a temperature within a range of 130° C. to 200° C.

14. The process of claim 1 , wherein the hydrogenation solvent composition comprises at least 90 wt. % water based on the weight of hydrogenation solvent composition.

15. The process of claim 1 , wherein the sFDCA composition comprises:

a) less than 1 wt. % solids;

b) dissolved FDCA in an amount of at least 7 wt. %; and

c) a hydrogenation solvent in an amount of at least 50 wt. %;

d) FFCA in an amount of at least greater than 0 wt. %;

in each case based on the weight of the sFDCA composition.

16. The process of claim 1 , wherein the sFDCA composition is fed to the hydrogenation reactor at a temperature within a range of 135° C.-200° C.

17. The process of claim 1 , wherein hydrogenation is conducted at a temperature within a range of 130° C. to less than 200° C.

18. The process of claim 1 , wherein the partial pressure of hydrogen is within a range of 50 psi to 500 psi.

19. The process of claim 1 , wherein hydrogenation is conducted under conditions effective to produce a pFDCA composition containing less than 500 ppm tetrahydrofuran dicarboxylic acid (“THFDCA”), based on the weight of FDCA solids in the pFDCA composition.

20. The process of claim 1 , wherein the hFDCA composition is crystallized.

21. The process of claim 1 , wherein the pFDCA composition comprises:

a) solids, wherein at least 98 wt. % of the solids are FDCA;

b) a b* of at least zero and less than 4;

c) FFCA in an amount of less than 200 ppm; and

d) tetrahydrofuran dicarboxylic acid (“THFDCA”) present in an amount ranging from 0 to 0.5 wt. %;

in each case based on the weight of the solids.

22. The process of claim 21 , wherein the pFDCA composition comprises at least 98 wt. % solids.

23. The process according to any one of claims 1 - 22 , wherein the hydrogenation solvent comprises at least 90 wt. % water.

24. The process of any one of claim 1 - 22 , wherein hydrogenation is conducted under a hydrogen partial pressure within a range of 10 psi to 900 psi and a total pressure within the hydrogenation reaction zone within a range of 35 psig to less than 950 psig.

25. The process of claim 24 , wherein the total pressure is within a range of 50 psig to 930 psig.

26. The process of claim 24 , wherein the hydrogen partial pressure is within a range of 20 psi to 400 psi.

27. The process of claim 1 , wherein the moles of FFCA fed into the hydrogenation reactor per hour to the moles of total catalyst metal(s) employed in the hydrogenation reactor is at least 0.1 hr −1 :1.

28. The process according to any one of claims 1 - 22 , wherein the yield of FDCA, on a solids basis and measured in the pFDCA composition, is at least 80%.

29. The process according to any one of claims 1 - 22 , wherein the process is operated to produce at least 20,000 kg/day of pFDCA on a solids basis, on a 24 hour basis over the course of any three months.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 27, 2013
From: JANKA, MESFIN EJERSSA; SUMNER, CHARLES EDWAN, JR.; KIRK, SHANE KIPLEY; SHAIKH, ASHFAQ SHAHANAWAZ; PARKER, KENNY RANDOLPH
To: EASTMAN CHEMICAL COMPANY
Reel/Frame 029882/0725 →
Continuity (2)
Provisional Application 61663246 · Jun 22, 2012
Related Publication 20130345452A1 · Dec 26, 2013