Flexible substrates comprising curable compositions containing acetoacetylated resins

Patent metadata

Field	Value
Publication number	US-11261359-B2
Application number	US-201916705365-A
Country	US
Kind code	B2
Filing date	Dec 6, 2019
Priority date	Dec 11, 2018
Publication date	Mar 1, 2022
Grant date	Mar 1, 2022

Abstract

This invention relates to an article of manufacture comprising at least one flexible substrate coated with at least one curable composition comprising:
I. a first component (I) comprising at least one resin having at least one functional group selected from the group consisting of β-ketoester and malonate functional groups, II. a second component (II) comprising at least one curing agent having at least one aldehyde functional group, and III. a third component (III) comprising at least one compound having amine functionality, salts thereof, or combinations thereof.

First claim

What is claimed is:

1. An article of manufacture comprising at least one flexible substrate coated with at least one curable composition comprising:
I. a first component (I) comprising at least one resin having at least one functional group selected from the group consisting of β-ketoester and malonate functional groups, wherein the resin is a either an amorphous polyester, a semi-crystalline polyester or a polyether, or a combination thereof, wherein Component (I) is at least one acetoacetate functional polyester comprising the residues of:

a. a hydroxyl component comprising:
i. at least one diol in an amount ranging from 0 to 100 mole % or 50 to 100 mole %, based on the total moles of (i) and (ii) equaling 100 mole %; and
ii. at least one polyol in an amount ranging from 0 to 100 mole % or 0 to 50 mole %, based on the total moles of (i) and (ii) equaling 100 mole %;

b. at least one carboxyl component comprising a polycarboxylic acid compound, a derivative of a polycarboxylic acid compound, or a combination thereof; and
c. at least one compound selected from an alkyl acetoacetate, a diketene, or a combination thereof,
II. a second component (II) comprising at least one curing agent having at least one aldehyde functional group, and
III. a third component (III) comprising at least one compound having amine functionality, salts thereof, or combinations thereof.

2. The article of manufacture of claim 1 wherein at least one said curable adhesive is applied to a first substrate and, optionally, is applied to a second substrate and wherein at least one substrate is selected from the group consisting of a metallic material, a plastic material, a composite material, a paper material, a fabric material, or combinations of two or more thereof.

3. The article of manufacture of claim 2 wherein at least one said curable composition is applied to a first substrate and, optionally, is applied to a second substrate and wherein at least one substrate is selected from the group consisting of cast polypropylene, metallized polypropylene, foil laminated polypropylene, polyethylene terephthalate, metallized polyethylene terephthalate, foil laminated polyethylene terephthalate, oriented polyethylene terephthalate, biaxially oriented polyethylene terephthalate, extruded polyethylene terephthalate, low density polyethylene, oriented polypropylene, biaxially oriented polypropylene, nylon, ethylene vinyl alcohol, and extruded films.

4. The article of manufacture of claim 1 wherein the curable composition is either solventless or contains at least one organic solvent.

5. The article of manufacture of claim 4 wherein said composition comprises 25 to 100%, or 25 to 95%, or 35 to 75%, or 35 to 80%, or 50 to 80%, or 55 to 75%, or 40 to 60% by weight solids.

6. The article of manufacture of claim 1 wherein said composition has a T-peel strength of at least 100 g/n as measured according to ASTM F904-16 “Standard Test Method for Comparison of Bond Strength or Ply Adhesion of Similar Laminates Made from Flexible Materials” when cured for one week at room temperature.

7. The article of manufacture of claim 6 wherein said curable composition is essentially solventless and has a Brookfield viscosity of 5000 cP or less when measured at 50° C. or less, or at room temperature when using ASTM D3236 Method, “Apparent Viscosity of Hot Melt Adhesives and Coating Materials”.

8. The article of manufacture of claim 6 , wherein said curable composition is solvent-based and has a Brookfield viscosity of 500 cP or less at application temperature, or at room temperature measured using ASTM D3236 Method, “Apparent Viscosity of Hot Melt Adhesives and Coating Materials”.

9. The article of manufacture of claim 1 wherein said amine is at least one amine having primary amine functionality or at least one amine having secondary amine functionality or combinations thereof.

10. The article of manufacture of claim 9 wherein said amine having primary amine functionality is first reacted with Component (I) and wherein the product thereof is then mixed with Component (II) and, after optional activation, curing said composition.

11. The article of manufacture of claim 9 wherein said at least one primary or at least one secondary amine are selected from at least one of: piperidine; piperazine; morpholine, pyrrolidine; ethylenediamine; diethylenetriamine; triethylenetetramine, or isomers thereof; tetraethylenepentamine or isomers thereof; 2,2,4-trimethylhexamethylenediamine; 1,2-diaminopropane; 1,3-diaminopropane; 1-ethyl-1,3-propanediamine; 2,2-dimethylpropylenediamine; 1,4-diaminobutane; 2-methylpentamethylenediamine; 1,6-hexanediamine; 1,7-diaminoheptane; 1,8-diaminooctane; 1,9-diaminononane; 1,12-diaminododecane; 4-azaheptamethylenediamine; N,N-bis(3-aminopropyl)butane-1,4-diamine; N,N-bis(3-aminopropyl)ethylenediamine; 2,4-toluenediamine; 2,6-toluenediamine; 3-dimethylaminopropylamine; 3-diethylaminopropylamine; 3,3′-iminobispropylamine; 1,2-diaminocyclohexane; 1,3-diaminocyclohexane; 1,4-diamino-2,5-diethylcyclohexane; 1,4-diamino-3,6-diethylcyclohexane; 1,2-diamino-4-ethylcyclohexane; 1,2-diamino-4-cyclohexylcyclohexane; isophorone diamine; norbomanediamine; 4,4′-diaminodicyclohexylmethane; 4,4′-diaminodicyclohexylethane; 4,4′-diaminodicyclohexylpropane; 2,2-bis(4-aminocyclohexyl)propane; 3,3′-dimethyl-4,4′-diaminodicyclohexylmethane; 3-amino-1-(4-aminocyclohexyl)propane; 1,3-bis(aminomethyl)cyclohexane; 1,4-bis(aminomethyl)cyclohexane; 1-cyclohexyl-3,4-diamino-cyclohexane; m-xylylenediamine and its hydrogenation products; p-xylylenediamine and its hydrogenation products; 4,4′-methylenedianiline; 2,4-bis(p-aminobenzyl)aniline; diethyltoluenediamine; m-phenylenediamine; 1,2,4-triazole; alanine; proline; 1,4,8,11-tetraazacyclotetradecane; diphenylethylenediamine, 2,2,4,4-tetramethylcyclobutane-1,3-diamine, 2,2-dimethylpropane-1,3-diamine, 2,3-dimethylbutane-2,3-diamine, 1,2-diaminocyclopentane, 1,2,2-trimethylcyclopentane-1,3-diamine, 1,7,7-trimethylbicyclo[2.2.1]heptane-2,3-diamine, dioctyl amine, diisopropylamine, and polyetheramines, or any isomers or combinations thereof.

12. The article of manufacture of claim 11 wherein at least one said amine is selected from the group consisting of triethylenetetramine, hexamethylene diamine, 2-methylpentamethylenediamine, and 3-dimethylaminopropylamine or any isomers thereof.

13. The article of manufacture of claim 11 wherein at least one said amine is selected from C1-C20 dialkyl amines.

14. The article of manufacture of claim 1 wherein the at least one amine and/or any reaction product thereof is present in the amount of up to 25 phr, or 0.1 to 10 phr, or 0.5 to 5 phr, or 0.5 to 2 phr, based on the total weight of Component (I), the resin.

15. The article of manufacture of claim 1 wherein at least one aldehyde of said composition is selected from at least one of 1,3-cyclohexanedicarboxaldehyde; 1,4-cyclohexanedicarboxaldehyde; mixtures of 1,3- and 1,4-cyclohexanedicarboxaldehyde; 2,6-norbomanedicarboxaldehyde; 2,5-norbornanedicarboxaldehyde; cyclododecane-1,4,8-tricarbaldehyde; 3-(4-formylcyclohexyl)propanal; tricyclodecane dialdehyde; o-phthalaldehyde; terephthalaldehyde; isophthalaldehyde; cyclopentane-1,3-dicarbaldehyde; cyclopenta-3,5-diene-1,3-dicarbaldehyde; glutaraldehyde; methylfurfural; furfural; or 5-(hydroxymethyl)furan-2-carbaldehyde; benzenedipropanal; or any isomers thereof; or combinations thereof.

16. The article of manufacture of claim 1 wherein the equivalent ratio of the acetoacetate (AcAc) functionality of Component (I) to the aldehyde functionality of said composition is

Assignees

• Eastman Chem Co

Inventors

• Boggs Monika Karin Wiedmann
• Collins Nick Allen
• Sharpe Robert Jacks
• Feng Ke
• Dougherty Shawn Marie
• Carvagno Terri Roxanne
• Kuo Thauming
• Burk Christopher Harlan
• Deng Liu
• Bhonde Vasudev R

Classifications

• C08G63/005

  Polyesters prepared from ketenes · CPC title

• C09D175/08

  from polyethers · CPC title

• C08J2323/12

  Polypropene · CPC title

• C09D7/65

  macromolecular (C09D7/41-C09D7/48 take precedence) · CPC title

• C09D167/02

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