Specific method for preparing biobased polyesters

Patent metadata

Field	Value
Publication number	US-9969840-B2
Application number	US-201515509498-A
Country	US
Kind code	B2
Filing date	Sep 10, 2015
Priority date	Sep 12, 2014
Publication date	May 15, 2018
Grant date	May 15, 2018

Abstract

The present invention relates to a method for preparing a linear or branched hydroxylated and/or carboxylated polyester resin that is free of unsaturated fatty acids, comprising reacting an acid component with an alcohol component, said acid component comprising at least one C4 to C6 polycarboxylic acid or anhydride, and at least one C8 to C54 polycarboxylic acid or anhydride, and said alcohol component comprising at least one biobased polyol having a functionality of at least 2 bearing a 1,4:3,6-dianhydrohexitol unit, and at least one of two polyols b2) and b3).

First claim

The invention claimed is:

1. A process for preparing a hydroxylated or carboxylated, optionally hydroxylated and carboxylated, linear or branched polyester resin free of unsaturated fatty acid, wherein said process comprises reaction between an acid component a) and an alcohol component b), with said acid component a) comprising:
a1) at least one C 4 to C 6 polycarboxylic acid or anhydride,
a2) at least one C 5 to C 54 polycarboxylic acid or anhydride, and
a3) optionally, at least one C 2 to C 22 saturated monoacid, and
with said alcohol component b) comprising:
b1) at least one biobased polyol having a functionality f b1 of at least 2, preferably 2, bearing a 1,4:3,6-dianhydrohexitol unit,
and at least one of two polyols b2) or b3):
b2) at least one polyol different than b1) having a functionality f b2 of at least 2,
b3) at least one polyol different than b1) and b2) having a functionality f b3 of at least 3,
with said reaction being carried out according to the following successive steps:
i) reaction of all of the acid component a) with said component b1) of said alcohol component b) until a conversion of at least 85%, of said component b1) is obtained, followed by
ii) reaction of the product resulting from step i) with the rest of said alcohol component b), comprising at least one of said polyols b2) or b3),
the reactions of said steps i) and ii) taking place in solution in at least one organic solvent which can form an azeotrope with water.

2. The process as claimed in claim 1 , wherein said step i) is carried out in the presence of a catalyst chosen from:
tin derivatives from tin oxalate, butylstannoic acid or tin(II) oxide, titanium derivatives from alkyl titanates.

3. The process as claimed in claim 2 , wherein the amount by weight of said catalyst relative to the weight of all of the reactants of step i) (a)+b1)) ranges from 0.01% to 0.5%.

4. The process as claimed in claim 1 wherein said step i) is carried out at a temperature ranging from 150 to 220° C.

5. The process as claimed in claim 1 wherein said step ii) is carried out at a temperature ranging from 180 to 250° C.

6. The process as claimed in claim 1 wherein said organic solvent is selected from the grow consisting of ketones, aromatic solvents, cycloaliphatic solvents, and alkanes which are at least C 7 alkanes.

7. The process as claimed in claim 1 wherein a fraction by weight of at least 50% of said polyol b) is biobased.

8. The process as claimed in claim 1 wherein said component b1) is chosen from the group consisting of isosorbide (1,4:3,6-dianhydro-D-sorbitol), isomannide (1,4:3,6-dianhydro-D-mannitol) and isoidide (1,4:3,6-dianhydro-L-iditol).

9. The process as claimed in claim 1 wherein at least 50% by weight relative to the overall weight of said components a)+b) is biobased.

10. The process as claimed in claim 1 wherein the components a) and b) are 100% biobased.

11. The process as claimed in claim 1 wherein said polyol b2) is biobased and chosen from the groups consisting of 1,3-propylenediol, 1,2-propylenediol, 1,4-butanediol, and dials based on saturated fatty acids.

12. The process as claimed in claim 1 wherein said polyol b3) is biobased and chosen from the group consisting of glycerol and ether-polyol derivatives thereof.

13. The process as claimed in claim 1 wherein said polyacid a1) is a biobased aliphatic diacid chosen from the group consisting of succinic acid, tartaric acid, citric acid, malic acid, itaconic acid, glutaric acid, glutamic acid, fumaric acid, furandicarboxylic acid, tetrahydrofuran-2,5-dicarboxylic acid and tetrahydrofuran-3,5-dicarboxylic acid.

14. The process as claimed in claim 1 wherein said polyacid a2) is biobased and chosen from the group consisting of azelaic acid (C 9 ), sebacic acid (C 10 ), undecanedioic acid, dodecanedioic acid and respectively C 36 and C 54 fatty acid dimers and trimers.

15. The process as claimed in claim 1 wherein said monoacid a3) is selected from the groom consisting of acetic acid, pyruvic acid, lactic acid, rosin (which means abietic acid and C 20 isomers) and a C 12 to C 22 saturated fatty acid.

16. The process as claimed in claim 1 wherein said polyol b1) represents at least 40 mol/mol % relative to the component b).

17. The process as claimed in claim 1 wherein during the first step i), the molar ratio of the carboxy groups of said component a) relative to the OH groups of said polyol b1) ranges from 1.1 to 2.1.

18. The process of claim 1 , wherein said at least one C 4 to C 6 polycarboxylic acid or anhydride has a functionality f a1 ranging from 2 to 4 and the at least one C 9 to C 54 polycarboxylic acid or anhydride has a functionality f a2 ranging from 2 to 4.

19. The process of claim 1 , wherein the said polyol b2) is a polyol in C 3 -C 36 .

20. The process of claim 1 , wherein f a1 =2, f a2 =2, f b1 =2, f b2 =2 and f b3 =3.

21. The process of claim 1 , wherein the reaction of all of the acid component a) with said component b1) of said alcohol component b) proceeds until a conversion of 100% of said component b1) is obtained.

22. The process of claim 2 , wherein said alkyl titanates are selected from the group consisting of ethyl titanate, isopropyl titanate, butyl titanate, and 2-ethylhexyl titanate.

23. The process of claim 22 , wherein said alkyl titanates are selected from the group consisting of isopropyl titanate and butyl titanate.

Assignees

• Arkema France

Inventors

• Cogordan Frank
• Ozeray Herve W
• Riondel Alain F

Classifications

• C08G63/672

  Dicarboxylic acids and dihydroxy compounds · CPC title

• C08G63/85

  Germanium, tin, lead, arsenic, antimony, bismuth, titanium, zirconium, hafnium, vanadium, niobium, tantalum, or compounds thereof {(C08G63/823 takes precedence)} · CPC title

• C08G63/916 Primary

  Dicarboxylic acids and dihydroxy compounds · CPC title

• C08G63/668 Primary

  derived from polycarboxylic acids and polyhydroxy compounds · CPC title