Curable polyester polyols and their use in thermosetting soft feel coating formulations

Patent metadata

Field	Value
Publication number	US-10011737-B2
Application number	US-201615078537-A
Country	US
Kind code	B2
Filing date	Mar 23, 2016
Priority date	Mar 23, 2016
Publication date	Jul 3, 2018
Grant date	Jul 3, 2018

Abstract

A soft feel curable polyester composition comprising the residues of a 2,2,4,4-tetraalkylcyclobutane-1,3-diol, a C 2 -C 20 diol other than 2,2,4,4-tetraalkylcyclobutane-1,3-diol, a C 2 -C 20 polyol, an alicyclic diacid and an acyclic aliphatic diacid, wherein said curable polyester contains at least 90 mole percent of aliphatic diacid residues, based on the total moles of diacid residues, and wherein said curable polyester has a hydroxyl number of about 100 to about 250 mgKOH/g, an acid number of 0 to about 30 mgKOH/g, and a number average molecular weight of about 500 to about 10,000 g/mole, a soft segment polyol, an isocyanate crosslinker and a solvent or a solvent mixture.

First claim

We claim:

1. A curable coating composition comprising:
A) a curable aliphatic polyester composition comprising the residues of:
i. a hydroxyl component, said hydroxyl component comprising the residues of:
a) from 30 to about 90 mole %, based on the total moles of a) and b) of 2,2,4,4-tetraalkylcyclobutane-1,3-diol represented by the structure

 wherein R1, R2, R3, and R4 each independently are C 1 to C 8 alkyls;
b) from 10 to 70 mole % based on the total moles of a) and b) of a C 2 -C 20 diol other than 2,2,4,4-tetraalkylcyclobutane-1,3-diol;
c) from 5 to 60 mole %, based on the total moles of a), b) and c) of a C 2 -C 20 polyol;

ii. a diacid component, said diacid component comprising the residues of:
d) from 70 to about 100 mole %, based on the total moles of d) and e) of an alicyclic diacid; and
e) from 0 to 30 mole %, based on the total moles of d) and e) of an acyclic aliphatic diacid; and

wherein said curable polyester contains at least 90 mole percent of aliphatic diacid residues, based on the total moles of diacid residues, and wherein said curable polyester has a hydroxyl number of about 100 to about 250 mgKOH/g, an acid number of 0 to about 30 mgKOH/g, and a number average molecular weight of about 500 to about 10,000 g/mole;
B) a polyol selected from polycarbonate diol, polytetramethylene glycol, or polycaprolactone;
C) a crosslinker; and
D) a solvent;
wherein said curable polyester (A) is present in an amount from 10 to 50 weight %; said polyol (B) is present in an amount of from 50 to 90 weight %, said crosslinker (C) is present in an amount of from 10 to 50 weight % based on the total weight of said polyester (A), said polyol (B) and said crosslinker (C) in said coating composition.

2. The composition of claim 1 wherein said C 1 to C 8 alkyls on said 2,2,4,4-tetraalkylcyclobutane-1,3-diol are linear, branched, or a combination of linear and branched alkyls.

3. The composition of claim 1 wherein said 2,2,4,4-tetraalkylcyclobutane-1,3-diol is 2,2,4,4-tetramethylcyclobutane-1,3-diol (TMCD), 2,2,4,4-tetraethylcyclobutane-1,3-diol, 2,2,4,4-tetra-n-propylcyclobutane-1,3-diol, 2,2,4,4-tetra-n-butylcyclobutane-1,3-diol, 2,2,4,4-tetra-n-pentylcyclobutane-1,3-diol, 2,2,4,4-tetra-n-hexylcyclobutane-1,3-diol, 2,2,4,4-tetra-n-heptylcyclobutane-1,3-diol, 2,2,4,4-tetra-n-octylcyclobutane-1,3-diol, 2,2-dimethyl-4,4-diethylcyclobutane-1,3-diol, 2-ethyl-2,4,4-trimethylcyclobutane-1,3-diol, 2,4-dimethyl-2,4-diethyl-cyclobutane-1,3-diol, 2,4-dimethyl-2,4-di-n-propylcyclobutane-1,3-diol, 2,4-n-dibutyl-2,4-diethylcyclobutane-1,3-diol, 2,4-dimethyl-2,4-diisobutylcyclobutane-1,3-diol, 2,4-diethyl-2,4-diisoamylcyclobutane-1,3-diol or mixtures thereof.

4. The composition of claim 1 wherein the alkyl portion of said b) C 2 -C 20 diol is branched or linear, saturated or unsaturated, aliphatic or cycloaliphatic and the hydroxyl group of said b) C 2 -C 20 diol is primary, secondary or tertiary.

5. The composition of claim 1 wherein said b) C 2 -C 20 diol is 2,2-dimethyl-1,3-propanediol, 1,2-cyclohexanedimethanol, 1,3-cyclohexanedimethanol, 1,4-cyclohexanedimethanol, 2,2,4-trimethyl-1,3-pentanediol, hydroxypivalyl hydroxypivalate, 2-methyl-1,3-propanediol, 2-butyl-2-ethyl-1,3-propanediol, 1,4-butanediol, and 1,6-hexanediol or mixtures thereof.

6. The composition of claim 1 wherein the alkyl portion of said c) C 2 -C 20 polyol is branched or linear, saturated or unsaturated, aliphatic or cycloaliphatic and having three or more hydroxyl groups and wherein the hydroxyl groups are primary, secondary, and/or tertiary.

7. The composition of claim 1 wherein said c) C 2 -C 20 polyol has at least two primary hydroxyl groups.

8. The composition of claim 1 wherein said alicyclic diacid is a cyclic aliphatic dicarboxylic acid or diester derivative of a cyclic aliphatic dicarboxylic acid, or an anhydride derivative of a cyclic aliphatic dicarboxylic acid, or a combination thereof.

9. The composition of claim 1 wherein said alicyclic diacid is, 1-4-cyclohexanedicarboxylic acid, 1,3-cyclohexanedicarboxylic acid, hexahydrophthalic anhydride (HHPA), tetrahydrophthalic anhydride, tetrachlorophthalic anhydride, 5-norbornene-2,3-dicarboxylic anhydride, 5-norbornene-2,3-dicarboxylic acid, 2,3-norbornanedicarboxylic acid, 2,3-norbornanedicarboxylic acid anhydride, and mixtures thereof.

10. The composition of claim 1 wherein said acyclic aliphatic diacid is an open-chain aliphatic dicarboxylic acid compound, or a diester derivative of aliphatic dicarboxylic acid compound, or an anhydride derivative of aliphatic dicarboxylic acid compound, or a combination thereof.

11. The composition of claim 1 wherein said acyclic aliphatic diacids is adipic acid, maleic anhydride, maleic acid, fumaric acid, itaconic anhydride, itaconic acid, citraconic anhydride, citraconic acid, dodecanedioic acid, sebacic acid, azelaic acid.

12. The coating composition of claim 1 wherein said crosslinker is toluene diisocyanate, isocyanurates of toluene diisocyanate, diphenylmethane 4,4′-diisocyanate, isocyanurates of 4,4′-diisocyanate, methylenebis-4,4′-isocyanatocyclohexane, isophorone diisocyanate, isocyanurates of isophorone diisocyanate, 1,6-hexamethylene diisocyanate, isocyanurates of 1,6-hexamethylene diisocyanate, 1,4-cyclohexane diisocyanate, p-phenylene diisocyanate, and triphenylmethane 4,4′,4″-triisocyanate, tetramethyl xylene diisocyanate, metaxylene diisocyanate, polyisocyanates and isocyanateterminated adducts of diols and polyols and mixtures thereof.

13. The coating composition of claim 1 further comprising one or more cross-linking catalysts present in the amount of about 0.01 to 5 weight percent based on the total weight of the resin solids in said coating composition.

14. The coating composition of claim 13 wherein said cross-linking catalyst is a tertiary amine, a tin compound or an organo-metallic compound or a mixture thereof.

15. The coating composition of claim 13 wherein said cross-linking catalyst is triethylene diamine, N-methyl morpholine, N-ethyl morpholine, diethyl ethanolamine, 1-methyl-4-dimethylamino ethyl piperazine, 3-methoxy-N-dimethyl propyl amine, N-dimethyl-N′-methyl isopropyl propylene diamine, N,N-diethyl-3-diethyl amino propylamine, N,N-dimethyl benzyl amine, dicyclohexylmethylamine, 2,4,6-tris dimethylaminomethylphenol, N,N-dimethyl cyclohexylamine, triethylamine, tri-n-butylamine, I,8-diaza-bichloro[5,40]-undecene-7 N-methyl diethanolamine, N,N-dimethyl ethanolamine, N,N-diethyl cyclohexylamine, N,N,N′N′-tetramethyl-ethylene diamine, I,4-diaza-bicyclo-[2,2,2]-octane N-methyl-N-dimethylaminoethyl-piperazine, bis-(N,N-diethylaminoethyl)-adipate, N,N-diethylbenzylamine, pentamethyldiethylene triamine, N,N,N′,N′-tetramethyl-I,3-butanediamine, 1,2-dimethylimidazole, 2-methylimidazole, stannous chloride, dibutyl tin di-2-ethyl hexoate, stannous octoate, dibutyl tin dilaurate, trimethyl tin hydroxide, dimethyl tin dichloride, dibutyl tin diacetate, dibutyl tin oxide, tributyl tin acetate, tetramethyl tin, dimethyl dioctyl tin, tin ethyl hexoate, tin laurate, dibutyl tin maleate, dioctyl tin diacetate; zinc octoate, phenyl mercuric propionate, lead octoate, lead naphthenate, and copper naphthenate or a mixture thereof.

16. The coating composition of claim 1 wherein said solvent is a ketone, an aromatic compound, an acetate, mineral spirits, a naphtha or mixtures thereof.

17. The coating composition of

Assignees

• Eastman Chem Co

Inventors

• Zhou Jianhui
• Baker Leslie Taylor

Classifications

• C09D169/00

  Coating compositions based on polycarbonates; Coating compositions based on derivatives of polycarbonates · CPC title

• C09D175/06

  from polyesters · CPC title

• C09D169/005 Primary

  Polyester-carbonates · CPC title

• C08G18/44

  Polycarbonates · CPC title

• C08G18/4202

  Two or more polyesters of different physical or chemical nature (C08G18/44 takes precedence) · CPC title