Aqueous epoxy ester emulsions

• US 4,480,058 A
• Filed: 01/06/1981
• Issued: 10/30/1984
• Est. Priority Date: 12/04/1980
• Status: Expired due to Term

• Current Assignee: The Glidden Company (Nouryon BV)
• Original Assignee: SCM Corporation (Heidelberg Materials AG)
• Inventors: Ting, Vincent W., Marcinko, Richard M.
• Primary Examiner(s): Kight, John
• Assistant Examiner(s): YARBROUGH, AMELIA
• Application Number:
  US06/222,933
• Time in Patent Office: 1,393 Days
• Field of Search: 525/119, 525/113, 525/530, 260/29.2 EP, 260/29.4 UA, 260/29.3, 260/29.6 NR, 523/404, 523/412
• US Class Current: 523/404
• CPC Class Codes: C08L 2666/04 Macromolecular compounds according to groups C08L7/00 - C08L49/00, or C08L55/00 - C08L57/00; Derivatives thereof
• CPC Class Codes: C09D 163/00 Coating compositions based on epoxy resins; Coating compositions based on derivatives of epoxy resins

Abstract

Sanitary coatings based on self-emulsifiable epoxy ester copolymers are produced by esterifying a solvent-soluble carboxyl polymer with an epoxy resin in an organic resin and in the presence of at least about 2% amine catalyst to provide a carboxyl-functional epoxy polymer which can be reacted with a base and dispersed into water.

Claims

1. A nongelled hydroxy ester copolymer composition substantially free of oxirane functionality comprising an acidic copolymer-epoxy resin hydroxy ester reaction product produced by esterifying an acidic copolymer with an epoxy resin in the presence of amine catalyst in amounts larger than 2% by weight of reactants subjected to esterification to avoid a useless gel, the epoxy resin being a mixture containing at least 5% by weight of aromatic polyether which is difunctional in oxirane functionality which is consumed by reaction with the acidic copolymer and the acidic copolymer being a solution copolymer of monoethylenically unsaturated monomers comprising at least about 20% of monoethylenically unsaturated carboxylic acid, based on the total weight of monomers, the epoxy resin mixture constituting at least about 40% of the total resin solids content and providing oxirane functionality in a stoichiometric deficiency with respect to carboxyl functionality in the acidic copolymer of from 1:

2 to 1;

20, at least a portion of the carboxyl functionality in the copolymer-epoxy resin hydroxy ester reaction product being reacted with a base to render the reaction product self-emulsifiable in water.

2. The composition of claim 1 wherein the monoethylenically unsaturated carboxylic acid is methacrylic acid.

3. The composition of claim 1 wherein the monoethylenically unsaturated monomers other than the monoethylenically unsaturated carboxylic acid are nonreactive.

4. The composition of any one of claims 1 to 3 wherein the monoethylenic carboxylic acid is present in an amount of from 30% to 80% based on the total weight of monomers.

5. The composition of claim 1 wherein the aromatic polyethers include at least 3% by weight of aromatic polyether carrying two glycidyl ether groups.

6. The composition of claim 1 wherein the aromatic polyethers include at least 10% by weight of aromatic polyether devoid of oxirane functionality.

7. The composition of claim 1 wherein the aromatic polyethers are terminated by either glycidyl ether groups or bisphenol groups.

8. The composition of claim 1 wherein the epoxy resin mixture is reacted with preformed acidic copolymer under esterification conditions to consume the oxirane functionality in the epoxy resin.

9. The composition of claim 1 wherein the composition further includes from 1-25% of curing agent selected from aminoplast resins, phenoplast resins, and mixtures thereof, based on the weight of total resin.

10. The composition of claim 1 wherein the epoxy resin is a mixture containing at least 10% by weight of bisphenolic polyether containing oxirane functionality, at least 3% by weight of the bisphenolic polyethers being diglycidyl ethers, and the oxirane functionality being consumed by reaction with the acidic copolymer, and at least 10% by weight of bisphenolic polyether devoid of oxirane functionality, and the acidic copolymer is a solution copolymer of mono-ethylenically unsaturated monomers comprising about 30% to about 70% of methacrylic acid, based on the total weight of monomers, the balance of the monomers being nonreactive, the epoxy resin mixture constituting at least about 50% of the total resin solids content and providing oxirane functionality in a stoichiometric deficiency with respect to carboxyl functionality in the acidic copolymer of from 1:

4 to 1;

10, from about 30% to about 90% of the carboxyl functionality in the copolymer-epoxy resin hydroxy ester reaction product being reacted with volatile amine to render the reaction product self-emulsifiable in water.

11. The composition of claim 10 wherein an aminoplast resin is present in an amount of from 2-12%, based on the total weight of resin.

12. A stable aqueous emulsion comprising the hydroxy ester copolymer composition of claim 1 dispersed in water.

13. The emulsion of claim 12 wherein amine is used to form a salt with 50% to 90% of the available carboxyl groups, and water is present in an amount to provide a solids content of 18% to 25%.

34. The nongelled hydroxy ester copolymer of claims 1, 8, or 10 wherein the epoxy resin is esterified with acidic copolymer in the presence of amine catalyst in amounts larger than 0.3% by weight of reactants to avoid a useless gel and provide a nongelled epoxy resin ester copolymer.

35. The nongelled hydroxy ester copolymer in claim 8 wherein the esterification conditions comprise the inclusion of amine esterification catalyst in amounts larger than 2% by weight of reactants to avoid a useless gel while forming said acidic copolymer-epoxy resin hydroxy ester reaction product.

36. The nongelled hydroxy ester copolymer of claim 34 being water dispersed by adding water to said hydroxy ester copolymer.

14. Process for preparing a self-emulsifiable epoxy ester copolymer mixture which comprises esterifying a solvent-soluble carboxy-functional polymer comprising polymerized ethylenically unsaturated monomers with an epoxy resin which is a mixture comprising aromatic polyethers containing oxirane functionality, at least 5% of the aromatic polyethers being constituted by diepoxide, the mixture of aromatic polyethers constituting at least 40% of the total resin solids content and providing oxirane functionality in a stoichiometric deficiency with respect to carboxyl functionality in the carboxyl-functional polymer of from 1:

2 to 1;

20, the esterification being carried out in organic solvent medium in the presence of greater than 2% of an amine esterification catalyst, based on the weight of the reactants subjected to esterification, and at an elevated temperature sufficient to cause the oxirane functionality to react with the carboxyl functionality until the oxirane functionality is substantially entirely consumed and reaching at least a portion of the carboxyl functionality in the resultant polymer-epoxy resin hydroxy ester reaction product with a base to render the reaction product self-emulsifiable in water.

15. The process of claim 14 wherein the esterification is carried out in alcoholic solvent medium.

16. The process of claim 14 wherein there is present more than one equivalent of oxirane functionality per molecule of carboxy-functional polymer.

17. The process of claim 14 in which the carboxyl-functional polymer is a solution copolymer of monoethylenically unsaturated monomers comprising at least about 20% of monoethylenically unsaturated carboxylic acid, based on the total weight of monomers.

18. The process of claim 17 wherein the monoethylenically unsaturated carboxylic acid is methacrylic acid.

19. The process of claim 18 wherein the monoethylenically unsaturated monomers other than the monoethylenically unsaturated carboxylic acid are nonreactive.

20. The process of claim 17 wherein the monoethylenically unsaturated carboxylic acid is present in an amount of from 30% to 80%, based on the total weight of monomers.

21. The process of claim 14 wherein the aromatic polyethers include at least 10% by weight of aromatic polyether devoid of oxirane functionality.

22. The process of claim 14 wherein the aromatic polyethers are terminated by groups selected from glycidyl ether groups, phenolic groups and benzoid acid groups.

23. The process of claim 14 wherein the aromatic polyethers are bisphenolic polyethers and the oxirane functionality is provided by glycidyl ether groups.

24. The process of claim 23 wherein the aromatic polyethers contain from 10% to 95% by weight of diglycidyl ethers.

25. The process of claim 14 wherein the amine esterification catalyst is used in an amount of from 4% to 10%.

26. The process of claim 25 wherein the amine esterification catalyst is dimethyl ethanolamine.

27. The process of claim 14 wherein the base is a volatile amine.

28. The process of claim 27 wherein the base is dimethylamino ethanol.

29. The product produced according to the process of claim 14.

37. The process of claim 14 wherein said epoxy ester copolymer is dispersed into water by reacting at least a portion of said non-esterified carboxyl groups on said epoxy ester copolymer with an amine base.

38. The process of claim 37 wherein the epoxy ester copolymer is dispersed into water by adding water to the epoxy ester copolymer and mixing to provide a stable nongelled water dispersed epoxy resin ester copolymer.

30. A process for producing a water-dispersed nongelled emulsion of an epoxy resin ester copolymer containing by weight at least about 40% epoxy resin esterified with an acidic copolymer, the process steps comprising:

esterifying epoxy resin with acid functional copolymer in the presence of at least about 4% by weight amine esterification catalyst based on reactants and carried out in an organic solvent medium, wherein said acid functional copolymer comprises copolymerized ethylenically unsaturated monomers including between 30% and 70% by weight monoethylenically unsaturated carboxylic acid whereby the acidic copolymer contains 4 to 10 carboxyl groups per epoxy resin oxirane groups and said epoxy resin ester copolymer contains non-esterified carboxyl groups;

reacting at least a portion of the non-esterified carboxyl groups on said epoxy resin ester copolymer with volatile amine base and dispersing the epoxy resin ester copolymer in water to provide a nongelled emulsion.

31. The process in claim 30 wherein the acid functional copolymer is formed by polymerizing said monomers in the presence of a minor amount of organic solvent.

32. The process in claim 30 wherein esterification of the epoxy resin with the acid functional polymer is carried out in the presence of a minor amount of organic solvent, and said amine esterification catalyst level is between 4% and 10%.

33. The process in claim 30 wherein the amine esterification catalyst dimethylaminoethanol.

39. A composition suitable for sanitary can coatings consisting essentially of a self-emulsified mixture substantially free of oxirane groups including a hydroxy ester copolymer containing carboxyl groups at least some of which, sufficient to achieve self-emulsification in water, are neutralized by volatile amine;

which composition is the product of the reaction of;

(A) an acidic addition copolymer having an acid number greater than 150 comprising a copolymer of monoethylenically unsaturated monomers selected from the group consisting of styrene, vinyl toluene, acrylic acid esters, methacrylic acid esters, acrylic acid and methacrylic acid containing at least about 30% by weight of acrylic or methacrylic acid based on the total weight of monomers;

(B) a mixture containing (bispenol-A)-epichlorohydrin polyether epoxy resin including at least 5% by weight of polyether epoxy resin containing oxirane groups and at least 25% by weight of said (bisphenol-A)polyether being terminated with bisphenol-A and devoid of oxirane groups, said mixture comprising at least 40% of the total resin solids and containing sufficient oxirane groups to provide a ratio of oxirane groups to carboxyl of 1;

2 to 1;

20; and

conducted in the presence of a tertiary amine in amounts larger than 2% by weight of reactants subjected to esterification.

40. The composition of claim 39 in which said acidic addition copolymer is the copolymer of monomers selected from the group consisting of styrene, vinyltoluene, acrylic acid esters, methacrylic acid esters and methacrylic acid.

41. The composition of claim 39 containing, in addition, 1-25 weight percent based on the total resin content, of a curing agent selected from the group consisting of aminoplast resins, phenoplast resins and mixtures thereof.

42. The composition of claim 39 in which said mixture (B) comprises at least 50% by weight of the total resins content, contains sufficient oxirane groups to provide a ratio of oxirane groups to carboxyl groups of 1:

4 to 1;

10, contains at least 10% by weight of polyether containing oxirane functionality, and contains at least 3% by weight of said polyethers being diglycidyl ethers;

said acidic copolymer comprising about 30% to about 70% of methacrylic acid based on the total weight of monomers, the balance of said monomers being nonreactive with oxirane groups; and

from about 30% to 90% of the carboxyl functionality in said copolymer hydroxy ester copolymer is reacted with a volatile amine to render composition self-emulsifiable in water.

43. A metal substrate coated with the composition of claims 39, 40, 41, or 42, and subsequently baked.