Zinc (1-methylimidazole)bis(2-ethylhexanoate) complex catalyzed coating material composition

Patent metadata

Field	Value
Publication number	US-10023764-B2
Application number	US-201314372614-A
Country	US
Kind code	B2
Filing date	Jan 24, 2013
Priority date	Jan 25, 2012
Publication date	Jul 17, 2018
Grant date	Jul 17, 2018

Abstract

Described are coating material compositions comprising an isocyanate group-containing component, a hydroxyl group-containing component, and a zinc (1-methylimidazole)bis(2-ethylhexanoate) complex. Also described is the use of a zinc (1-methylimidazole)bis(2-ethylhexanoate) complex as a catalyst system for the urethane reaction in coating material compositions.

First claim

What is claimed is:

1. A coating material composition consisting essentially of:
at least one polyhydroxyl group-containing component (A) and optionally at least one low molecular mass polyol compound (C);
at least one polyisocyanate group-containing component (B);
a catalyst system consisting of:
a) at least one zinc (1-methylimidazole)bis(2-ethylhexanoate) complex (D) having the general formula [Zn(1-methylimidazole) n (2-ethylhexanoate) 2 ], wherein n≥1 to ≤2; and
b) at least one monomeric aromatic carboxylic acid (S), wherein the carboxyl group is in conjugation to a pi electron system;

optionally, one or more amino resins and/or one or more tris(alkoxycarbonylamino)triazines (E);
optionally, pigments and/or fillers; and
optionally, organic solvents and/or water.

2. A coating material composition comprising:
at least one polyhydroxyl group-containing component (A);
at least one polyisocyanate group-containing component (B);
at least one low molecular mass polyol compound (C); and
a catalyst system consisting of
a) at least one zinc (1-methylimidazole)bis(2-ethylhexanoate) complex (D) having the general formula [Zn(1-methylimidazole) n (2-ethylhexanoate) 2 ], wherein n≥1 to ≤2; and b) at least one monomeric aromatic carboxylic acid (S), wherein the carboxyl group is in conjugation to a pi electron system;

wherein the coating composition exhibits improved processing life as compared to a coating material composition containing a dibutyl tin laurate catalyst and the at least one monomeric aromatic carboxylic acid (S), and;
wherein the coating material composition exhibits a shorter drying time and earlier achievement of assembly strength as compared to a coating material composition containing the zinc (1-methylimidazole)bis(2-ethylhexanoate) complex (D) without benzoic acid.

3. The coating material composition of claim 2 , wherein the at least one polyhydroxyl group-containing component (A) comprises a poly(meth)acrylate polyol and/or a polyester resin.

4. The coating material composition of claim 2 , wherein the polyisocyanate group-containing component (B) comprises 1,6-hexamethylene diisocyanate, isophorone diisocyanate, or 4,4′-methylenedicyclohexyl diisocyanate, their biuret dimers and/or their isocyanurate trimers and/or their asymmetric trimers.

5. The coating material composition of claim 2 , wherein the at least one monomeric aromatic carboxylic acid (S) comprises benzoic acid, tert-butylbenzoic acid, 3,4-dihydroxybenzoic acid, salicylic acid and/or acetylsalicylic acid.

6. The coating material composition of claim 2 , wherein the at least one zinc (1-methylimidazole)bis(2-ethylhexanoate) complex (D) is present in an amount such that the metal content of the zinc (1-methylimidazole)bis(2-ethylhexanoate) complex, based in each case on the binder fraction of the coating material, is between 35 and 2000 ppm, and/or the coating material comprises 0.2% to 15.0%, by weight, of at least one monomeric carboxylic acid (S), the percentages by weight again each being based on the binder fraction of the coating material.

7. The coating material composition of claim 2 , wherein the at least one low molecular mass polyol compound (C) is different from component (A), and/or wherein the molar equivalent ratio of the hydroxyl groups of the hydroxyl-containing compound (A) plus (C) to the isocyanate groups of component (B) is between 1:0.9 and 1:1.5.

8. The coating material composition of claim 2 , wherein the coating material composition is a nonaqueous coating material and/or comprises pigments.

9. A catalyst system consisting of at least one zinc (1-methylimidazole)bis(2-ethylhexanoate) complex (D) and at least one monomeric aromatic carboxylic acid (S) in which the carboxyl group is in conjugation to a pi electron system, wherein the catalyst system catalyzes a urethane reaction in a coating material composition comprising at least one polyisocyanate group-containing component and at least one polyhydroxyl group-containing component.

10. A coating material composition consisting essentially of the catalyst system of claim 9 , the at least one polyhydroxyl group-containing component (A) and the at least one polyisocyanate group-containing component (B).

11. A method of coating, the method comprising producing a coat of the coating material composition of claim 2 on an automobile.

12. A multistage coating method, comprising applying, to an uncoated or precoated substrate, a pigmented basecoat film and thereafter a coat of the coating material composition of claim 2 .

13. The multistage coating method of claim 12 , wherein, following application of the pigmented basecoat film, the applied basecoat is first dried at temperatures from 23° C. room temperature to 80° C. and, following the application of the coating material, is cured at temperatures between 20 and 80° C.

14. A method of coating, the method comprising coating a substrate with a clearcoat or pigmented paint comprising the coating composition of claim 2 , wherein the substrate comprises one or more of an automotive surface, a parts surface, a plastics substrate, or a utility vehicle surface.

15. The method of claim 12 , wherein the substrate comprises one or more of an automotive surface, a plastic substrate, or an utility vehicle surface.

16. An automobile coating comprising at least one coat of the coating material composition of claim 2 .

17. A multistage coating method, comprising applying, to an uncoated or precoated substrate, a pigmented basecoat film and thereafter applying a coating material composition produced through use of the catalyst system of claim 9 .

18. The multistage coating method of claim 17 , wherein, following application of the pigmented basecoat film, the applied basecoat is first dried at temperatures from 23° C. room temperature to 80° C. and, following the application of the coating material composition, is cured at temperatures between 20 and 80° C.

19. The coating material composition of claim 3 , wherein the polyhydroxyl group-containing component (A) comprises a poly(meth)acrylate polyol.

20. The coating material composition of claim 5 , wherein at least one monomeric aromatic carboxylic acid (S) component of the catalyst system is benzoic acid.

21. The coating material composition of claim 7 , wherein the molar equivalent ratio of the hydroxyl groups of the hydroxyl-containing compound (A) plus, where appropriate, (C) to the isocyanate groups of component (B) is between 1:0.95 and 1:1.05.

22. The multistage coating method of claim 17 , wherein catalysis is carried out at a temperature in the range of from 20 to 60° C.

23. A method for extending processing life of a coating material composition which comprises at least one polyisocyanate group-containing component and at least one polyhydroxyl group-containing component, the method comprising the step of adding to the coating material composition a catalyst system consisting of at least one zinc (1-methylimidazole)bis(2-ethylhexanoate) complex (D) and at least one monomeric aromatic carboxylic acid (S) in which the carboxyl group is in conjugation to a pi electron system.

24. The method according to claim 23 wherein at least one monomeric aromatic carboxylic acid (S) component of the catalyst system is benzoic acid.

25. The coating material composition according to claim 1 , wherein the at least one low molecular mass polyol compound (C) is selected from the group consist

Assignees

• Basf Coatings Gmbh

Inventors

• Hsieh Bing
• Coughlin Robert D
• Ravichandran Ramanathan
• Abi-Karam Farouk
• Westhoff Elke
• Hoffmann Peter
• Möller Bernadette
• Schnier Benedikt

Classifications

• B05D1/02

  performed by spraying · CPC title

• C08G18/792

  formed by oligomerisation of aliphatic and/or cycloaliphatic isocyanates or isothiocyanates · CPC title

• C08G18/222

  metal compounds not provided for in groups C08G18/225 - C08G18/26 · CPC title

• C08G18/166

  Catalysts not provided for in the groups C08G18/18 - C08G18/26 · CPC title

• B05D1/04

  involving the use of an electrostatic field {(B05D1/025 and B05D1/14 take precedence)} · CPC title