IP Library › Granted Patent US 9,890,242
Granted Patent B2
US 9,890,242 · App. 15/122,694 · Granted Feb 13, 2018

Polyester and method for preparing such a polyester

Inventors: Jeffrey John Kolstad (Amsterdam, NL); Gerardus Johannes Maria Gruter (Amsterdam, NL); Matheus Adrianus Dam (Amsterdam, NL); Bing Wang (Amsterdam, NL); Robert Joseph Schiavone (Matthews, NC); Marion L. Andrews (Darlington, SC); Jesper Gabriël van Berkel (Amsterdam, NL); Edward E. Paschke (Galena, IL)
Assignee: Synvina C.V.
C08G63/181C08G63/78C08G63/80C08G63/866
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Quick Facts
Patent No.
US 9,890,242
App. No.
15/122,694
Granted
Feb 13, 2018
Kind
B2
Abstract

A polyester, including ethylene 2,5-furandicarboxylate units, has an intrinsic viscosity of at least 0.45 d L/g, and has a relative content of carboxylic acid end groups, expressed as the fraction of the molar amount of carboxylic acid end groups divided by the sum of the molar amounts of hydroxyl end groups and carboxylic acid end groups in the range of 0.10 to 0.70. The polyester can be prepared with a method wherein a starting mixture comprising 2,5-furandicarboxylic acid and ethylene glycol is subjected to esterification and subsequent polycondensation at reduced pressure when the molar ratio of 2,5-furandicarboxylic acid to ethylene glycol in the starting mixture is 1:1.01 to 1:1.15, where water, that is formed during the reaction between 2,5-furandicarboxylic acid and ethylene glycol, and some ethylene glycol are removed in a distillation system, and where ethylene glycol that is removed with water, is separated from water and at least partly recycled.

Claims (20)

1. A polyester comprising ethylene 2,5-furandicarboxylate units, which polyester has an intrinsic viscosity of at least 0.45 dL/g, and which polyester has a relative content of carboxylic acid end groups, expressed as the fraction of the molar amount of carboxylic acid end groups divided by the sum of the molar amounts of hydroxyl end groups and carboxylic acid end groups, in the range of 0.10 to 0.70.

2. The polyester according to claim 1 , which has an intrinsic viscosity of at most 1.0 dL/g.

3. The polyester according to claim 1 , wherein the relative content of carboxylic acid end groups is in the range of 0.14 to 0.65.

4. The polyester according to claim 1 , wherein the amount of carboxylic acid end groups is in the range of 15 to 122 meq/kg.

5. The polyester according to claim 1 , which has a light absorbance of at most 0.08, measured as a 30 mg/mL solution in a dichloromethane:hexafluoroisopropanol 8:2 (vol/vol) mixture at 400 nm.

6. The polyester according to claim 1 , which has a polydispersity index in the range of 1.9 to 2.6.

7. The polyester according to claim 1 , which has a crystallinity of at least 25 J/g, measured by Differential Scanning Calorimetry (DSC).

8. The polyester according to claim 7 , which has a melting point of at least 215° C.

9. A composition comprising the polyester according to claim 1 , which has a moisture content of at most 100 ppmw.

10. A method for the preparation of a polyester, wherein a starting mixture comprising 2,5-furandicarboxylic acid and ethylene glycol is subjected to esterification to form an ester composition, wherein the molar ratio of 2,5-furandicarboxylic acid to ethylene glycol in the starting mixture is 1:1.01 to 1:1.15; and

wherein the ester composition thus obtained is subjected to polycondensation at reduced pressure in the presence of a polycondensation catalyst to obtain a polycondensate, wherein water, that is formed during the reaction between 2,5-furandicarboxylic acid and ethylene glycol, and some ethylene glycol are removed in a distillation system, and wherein ethylene glycol that is removed with water is separated from water and at least partly recycled.

11. The method according to claim 10 , wherein the esterification reaction between 2,5-furandicarboxylic acid and ethylene glycol is carried out at a temperature of 160 to 240° C. and a pressure of 0.9 to 5 bar for a period of 0.5 to 4 hr.

12. The method according to claim 10 , wherein the polycondensation comprises a pre-polycondensation reaction conducted at a pressure of 20 to 700 mbar and a polycondensation reaction conducted at a pressure of 0.05 to 20 mbar.

13. The method according to claim 12 , wherein the combined period for the pre-polycondensation and the polycondensation reactions is in the range of 1.5 to 4 hours.

14. The method according to claim 10 , wherein during the polycondensation step ethylene glycol that is formed is removed from the ester composition that is subjected to polycondensation.

15. The method according to claim 10 , wherein the polycondensation step is carried out in the presence of a polycondensation catalyst.

16. The method according to claim 15 , wherein the polycondensation catalyst is selected from the catalysts comprising one or more elements selected from tin, zinc, titanium, antimony.

17. The method according to claim 10 , wherein the polycondensation is carried out at a temperature of 245 to 270° C. and a pressure of 0.05 to 5 mbar.

18. The method according to claim 10 , wherein the polycondensate is crystallized at a temperature in the range of 90 to 200° C.

19. The polyester according to claim 1 , which has an intrinsic viscosity in the range of 0.45 to 0.75 dL/g.

Assignments (3)
DEED OF CONFIRMATION - PLEDGE OF FURTHER PATENT RIGHTS Recorded Jan 5, 2023
From: FURANIX TECHNOLOGIES B.V.
To: ABN AMRO BANK N.V.
Reel/Frame 062294/0740 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 4, 2020
From: SYNVINA C.V.
To: FURANIX TECHNOLOGIES B.V.
Reel/Frame 052005/0498 →
NUNC PRO TUNC ASSIGNMENT Recorded Dec 28, 2017
From: FURANIX TECHNOLOGIES B.V.
To: SYNVINA C.V.
Reel/Frame 044495/0958 →
Priority Claims (1)
NL 2012406 · Mar 11, 2014 · national
Continuity (2)
Provisional Application 61951213 · Mar 11, 2014
Related Publication 20170066870A1 · Mar 9, 2017