Thermosetting compositions based on phenolic resins and curable poleyester resins made with diketene or beta-ketoacetate containing compounds

Patent metadata

Field	Value
Publication number	US-9598602-B2
Application number	US-201414540490-A
Country	US
Kind code	B2
Filing date	Nov 13, 2014
Priority date	Nov 13, 2014
Publication date	Mar 21, 2017
Grant date	Mar 21, 2017

Abstract

A thermosetting composition having:
I. a curable polyester resin containing beta-ketoacetate moieties without vinyl unsaturations; and II. a phenolic resin having at least one methylol group.

The curable polyester resin can be made by reacting a polyester resin with a compound containing a beta-ketoacetate moiety that does not contain a vinyl unsaturation such as alkyl acetoacetate compounds or diketene compounds.
The curable polyester resin can be dispersed in water or dissolved in a solvent and is suitable for waterborne or solventborne coating compositions. Phenolic based crosslinking coating compositions that contain these curable polyester resins cure well with phenolic resin crosslinking compounds.

First claim

What we claim is:

1. A thermosetting composition, comprising:
I) a curable polyester resin comprising the reaction product of a polyester resin with a compound containing a beta-ketoacetate moiety that does not contain a vinyl unsaturation, said polyester resin comprising the reaction product of:
a) polyhydroxyl compounds comprising:
(i) diol compounds in an amount of 70 mole %-100 mole %; and
(ii) polyhydroxyl compounds having 3 or more hydroxyl groups in an amount of 0 to 30 mole %;
wherein the mole % is based on 100% of all moles of polyhydroxyl compounds a); and

b) polycarboxyl compounds comprising polycarboxylic acid compounds, derivatives of polycarboxylic acid compounds, the anhydrides of polycarboxylic acids, or combinations thereof; and

II) a phenolic resin substituted with at least one methylol group, wherein the phenolic resin is obtained by the reaction of phenolic compounds and an aldehyde at an aldehyde:phenol ratio of at least 1.1:1 and wherein the phenolic resin has at least one methylol substituent in the ortho position relative to the phenolic hydroxyl group.

2. The thermosetting composition of claim 1 , wherein the phenolic resin contains an average of at least one methylol substituent per phenolic hydroxyl group.

3. The thermosetting composition of claim 1 , wherein the phenolic resin is the reaction product of phenolic compounds with formaldehyde.

4. The thermosetting composition of claim 1 , wherein the phenolic resin is not made by the addition of bisphenol A, F, or S.

5. The thermosetting composition of claim 1 , wherein the phenolic resin is not made by the addition of a polyhydric phenol.

6. The thermosetting composition of claim 1 , wherein the curable polyester does not contain vinyl unsaturation and does not contain alkyd residues.

7. The thermosetting composition of claim 1 , wherein said compound having a beta-ketoacetate moiety comprises a compound represented by the following formula:

wherein R is a branched or straight chain, saturated or unsaturated alkyl, alicyclic, or aromatic group; R′ is a hydrogen or a branched or straight chain, saturated or unsaturated alkyl, alicyclic, or aromatic group; Z is a branched or straight chain, saturated or unsaturated alkyl, alicyclic, or aromatic group; , and wherein R does not contain a vinyl unsaturation.

8. The thermosetting composition of claim 7 , wherein R is a branched or straight chain alkyl group having 1-4 carbon atoms, R′ is a hydrogen or a branched or straight alkyl having 1-4 carbon atoms; and Z is a branched or straight chain alkyl having 1-8 carbon atoms.

9. The thermosetting composition of claim 1 , wherein the compound having a beta-ketoacetate moiety has molecular weight of less than 200.

10. The thermosetting composition of claim 1 , wherein the compound having a beta-ketoacetate moiety corn prises diketene or an alkyl acetoacetate compound.

11. The thermosetting composition of claim 1 , wherein the compound having a beta-ketoacetate moiety comprises t-butyl acetoacetate, ethyl acetoacetate, methyl acetoacetate, isobutyl acetoacetate, isopropyl acetoacetate, n-propyl acetoacetate, n-butyl acetoacetate, t-anyl acetotacetate, or diisopropyl carbinol acetoacetate.

12. The thermosetting composition of claim 1 , wherein the compound having a beta-ketoacetate moiety comprises t-butyl acetoacetate.

13. The thermosetting composition of claim 1 , wherein the thermosetting composition comprises said polyester resin (I) in an amount of 70 to 97 wt. % and said phenolic resin (II) in an amount of 3 to 30 wt. %, based on the total weight of (I) and (II).

14. The thermosetting composition of claim 1 , wherein the polycarboxylic acid compounds (b) comprise isophthalic acid, dimethyl isophthalate, terephthalic acid, dimethyl terephthalate, phthalic acid, phthalic anhydride, 1,4-cyclohexanedicarboxylic acid, 1,3-cyclohexanedicarboxylic acid, adipic acid, 2,6-naphthalenedicarboxylic acid, 1,4-naphthalenedicarboxylic acid, 2,5-naphthalene-dicarboxylic acid, hexahydrophthalic anhydride, tetrahydrophthalic anhydride, trimellitic anhydride, succinic anhydride, succinic acid, or mixtures thereof.

15. The thermosetting composition of claim 14 , wherein the polycarboxylic acid compounds (b) comprise isophthalic acid, dimethyl isophthalate, phthalic acid, phthalic anhydride, 1,4-cyclohexanedicarboxylic acid, adipic acid, hexahydrophthalic anhydride, tetrahydrophthalic anhydride, trimellitic anhydride, or mixtures thereof.

16. The thermosetting composition of claim 1 , wherein the poycarboxylic acid compounds (b) do not include terephthalic acid or a derivative of terephthalic acid.

17. The thermosetting composition of claim 1 , wherein all of the polyhydroxyl compounds (a) are hydrocarbons and do not contain atoms other than hydrogen, carbon and oxygen.

18. The thermosetting composition of claim 1 , wherein the diols (a)(i) comprise 2,2,4,4-tetraalkylcyclobutane-1,3-diol (TACD).

19. The thermosetting composition of claim 1 , wherein the diols (a)(i) comprise 2,2-dimethyl-1,3-propanediol (neopentyl glycol).

20. The thermosetting composition of claim 1 , wherein the diols (a)(i) are present in an amount of 80 to 98 mole %, based on 100 mole % of all polyhydroxyl compounds (a).

21. The thermosetting composition of claim 1 , wherein the polyhydroxyl compounds comprise polyhydroxyl compounds (a)(ii) having 3 or more hydroxyl groups, said polyhydroxyl compounds (a)(ii) comprising 1,1,1-trimethylol propane, 1,1,1-trimethylolethane, glycerin, pentaerythritol, erythritol, threitol, dipentaerythritol, sorbitol, or mixtures thereof.

22. The thermosetting composition of claim 1 , wherein the amount of polyhydroxyl compounds (a)(ii) is 2 to 15 mole %, based on 100 mole % of all polyhydroxyl compounds (a).

23. The thermosetting composition of claim 1 , wherein none of the polyhydroxyl compounds (a) contain any ester or carboxyl (—COO—) groups.

24. The thermosetting composition of claim 1 , wherein none of the polyhydroxyl compounds (a) have any carbonyl groups (—CO—).

25. The thermosetting composition of claim 1 , wherein none of the polyhydroxyl compounds (a) contain any ether groups.

26. The thermosetting composition of claim 1 , wherein the compound having a beta-ketoacetate moiety is reacted with the polyester resin in an amount of 3 to about 40 wt. % based on the based on the weight of the compound and the polyester resin.

27. The thermosetting composition of claim 1 , wherein the polyester resin has a hydroxyl number of 50-240 mg KOH/g, and at least 70% of the hydroxyl groups on the polyester resin are consumed with the residues of the compound having the beta-ketoacetate moiety.

28. The thermosetting composition of claim 1 , wherein the curable polyester (I) has an acid number in a range of 0-10 mg KOH/g.

29. The thermosetting composition of claim 1 , wherein the polyester resin used to make the curable polyester (I) has a hydroxyl number in the range of 30-240 mgKOH/g.

30. The thermosetting composition of claim 29 , wherein said polyester resin has a hydroxyl number in a range of 80-240 mg KOH/g.

31. The thermosetting composition of claim 30 , wherein said polyester resin has a hydroxyl number in a range of 80-150 mq KOH/g.

Assignees

• Eastman Chem Co

Inventors

• Kuo Thauming
• Hall Phillip Bryan

Classifications

• C09D161/06

  of aldehydes with phenols · CPC title

• C09D167/02 Primary

  Polyesters derived from dicarboxylic acids and dihydroxy compounds (C09D167/06 takes precedence) · CPC title

• C08G63/916

  Dicarboxylic acids and dihydroxy compounds · CPC title

• C08L61/28

  with melamine · CPC title

• C08L67/02

  Polyesters derived from dicarboxylic acids and dihydroxy compounds (C08L67/06 takes precedence) · CPC title