Solvent-borne coating compositions, coatings formed therefrom, and methods of forming such coatings

Patent metadata

Field	Value
Publication number	US-2024067842-A1
Application number	US-202318493843-A
Country	US
Kind code	A1
Filing date	Oct 25, 2023
Priority date	Nov 1, 2018
Publication date	Feb 29, 2024
Grant date	—

Abstract

A coating composition includes: (a) a carboxylic acid functional polyol polymer; (b) a melamine-formaldehyde crosslinker reactive with the carboxylic acid functional polyol polymer; (c) an acid catalyst; and (d) a non-aqueous liquid medium. The carboxylic acid functional polyol polymer has an acid value within a range of from 30 to 120 mg KOH/g and a hydroxyl value within a range of from 60 to 150 mg KOH/g. The melamine-formaldehyde crosslinker includes imino and methylol groups that together make up 35 mole % or less of the total functionality of the melamine-formaldehyde crosslinker, and butyl groups and isobutyl groups that together make up 5 mole % or greater of the total functionality of the melamine-formaldehyde crosslinker. The coating composition cures at a temperature of 90° C. or less.

First claim

The invention claimed is:

1 . A coating composition comprising:
(a) a carboxylic acid functional polyol polymer comprising an acid value within a range of from 30 to 120 mg KOH/g and a hydroxyl value within a range of from 60 to 150 mg KOH/g; (b) a melamine-formaldehyde crosslinker reactive with the carboxylic acid functional polyol polymer, wherein the melamine-formaldehyde crosslinker comprises imino and methylol groups that together comprise 35 mole % or less of the total functionality of the melamine-formaldehyde crosslinker, and wherein the melamine-formaldehyde crosslinker comprises butyl groups and isobutyl groups that together comprise 5 mole % or greater of the total functionality of the melamine-formaldehyde crosslinker; (c) an acid catalyst; and (d) a non-aqueous liquid medium, wherein the coating composition cures at a temperature of 90° C. or less.

2 . The coating composition of claim 1 , wherein the carboxylic acid functional polyol polymer is obtained from reactants comprising: (i) an ethylenically unsaturated compound comprising hydroxyl functional groups; (ii) an ethylenically unsaturated compound comprising carboxylic acid functional groups, or an anhydride thereof; and (iii) an ethylenically unsaturated compound that is different from (i) and (ii).

3 . The coating composition of claim 1 , wherein the acid catalyst comprises 5 weight % or less of the coating composition, based on the total solids weight of all hydroxyl functional polymers in the coating composition.

4 . The coating composition of claim 1 , wherein the melamine-formaldehyde crosslinker comprises from 12 to 30 weight % of the coating composition, based on the resin solids weight of the coating composition.

5 . The coating composition of claim 1 , wherein the carboxylic acid functional polyol polymer has an acid value within a range of from 50 to 95 mg KOH/g.

6 . The coating composition of claim 1 , wherein the carboxylic acid functional polyol polymer has a hydroxyl value within a range of from 60 to 100 mg KOH/g.

7 . The coating composition of claim 1 , wherein the carboxylic acid functional polyol polymer has glass transition temperature within a range of from −20 to 50° C.

8 . The coating composition of claim 1 , wherein the carboxylic acid functional polyol polymer has a weight average molecular weight of greater than 5,000 g/mol.

9 . The coating composition of claim 2 , wherein the ethylenically unsaturated compound comprising hydroxyl functional groups comprises at least 10 weight % of the reactants, based on the total solids weight of the reactants used to form the carboxylic acid functional polyol polymer.

10 . The coating composition of claim 2 , wherein the ethylenically unsaturated compound comprising carboxylic acid functional groups, or the anhydride, comprises at least 5 weight % of the reactants, based on the total solids weight of the reactants used to form the carboxylic acid functional polyol polymer.

11 . The coating composition of claim 2 , wherein the ethylenically unsaturated compound that is different from (i) and (ii) comprises a multi-ethylenically unsaturated compound, a mono-ethylenically unsaturated compound having an abstractable hydrogen, or a combination thereof.

12 . The coating composition of claim 11 , wherein the ethylenically unsaturated compound that is different from (i) and (ii) comprises at least two different mono-ethylenically unsaturated compounds having an abstractable hydrogen.

13 . The coating composition of claim 2 , wherein the ethylenically unsaturated compound that is different from (i) and (ii) comprises at least 50 weight % of the reactants, based on the total solids weight of the reactants used to form the carboxylic acid functional polyol polymer.

14 . The coating composition of claim 1 , wherein the coating composition cures at a temperature of 80° C. or less.

15 . A substrate at least partially coated with a coating formed from the coating composition of claim 1 .

16 . The substrate of claim 15 , wherein the coating composition is applied directly over at least a portion of the substrate.

17 . The substrate of claim 15 , wherein the coating composition is applied over at least a portion of a first coating layer formed over at least a portion of the substrate.

18 . A method of forming a coating over at least a portion of a substrate comprising:
applying a coating composition over at least a portion of a substrate, the coating composition comprising: (a) a carboxylic acid functional polyol polymer comprising an acid value within a range of from 30 to 120 mg KOH/g and a hydroxyl value within a range of from 60 to 150 mg KOH/g; (b) a melamine-formaldehyde crosslinker reactive with the carboxylic acid functional polyol polymer of (a), wherein the melamine-formaldehyde crosslinker comprises imino and methylol groups that together comprise 35 mole % or less of the total functionality of the melamine-formaldehyde crosslinker, and wherein the melamine-formaldehyde crosslinker comprises butyl groups and isobutyl groups that together comprise 5 mole % or greater of the total functionality of the melamine-formaldehyde crosslinker; (c) an acid catalyst; and (d) a non-aqueous liquid medium; and curing the coating composition at a temperature of 90° C. or less to form a coating over at least of portion of the substrate.

19 . The method of claim 18 , wherein the coating composition is cured at a temperature of 80° C. or less to form a coating over at least of portion of the substrate.

20 . The method of claim 18 , further comprising applying one or more additional coating compositions as a wet-on-wet process before or after applying the coating composition comprising components (a)-(d), and curing the coating compositions simultaneously.

Assignees

• Ppg Ind Ohio Inc

Inventors

• Wo Yaqi
• Fenn David R
• Luchansky Matthew S
• Swarup Shanti
• Wargo Diane L
• Xu Xiangling

Classifications

• C09D133/08 Primary

  Homopolymers or copolymers of acrylic acid esters · CPC title

• B05D7/542

  the two layers being cured or baked together · CPC title

• C08F220/06

  Acrylic acid; Methacrylic acid; Metal salts or ammonium salts thereof · CPC title

• C08F220/1808

  C8-(meth)acrylate, e.g. isooctyl (meth)acrylate or 2-ethylhexyl (meth)acrylate · CPC title

• C08F220/1811

  C10or C11-(Meth)acrylate, e.g. isodecyl (meth)acrylate, isobornyl (meth)acrylate or 2-naphthyl (meth)acrylate · CPC title