IP Library Granted Patent US 7,683,105
Granted Patent B2
US 7,683,105 · App. 11/816,776 · Granted Mar 23, 2010

Mixture containing a solvent, which can be cured with UV-A radiation, method for its production, and use thereof

Assignee: BASF Coatings AG
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Quick Facts
Patent No.
US 7,683,105
App. No.
11/816,776
Granted
Mar 23, 2010
Kind
B2
Abstract

A UV-A-curable, solvent-containing composition composed of (A) 1% to 50% by weight of a UV-A-curable constituent containing isocyanate-reactive groups; (B) 0.01% to 10% by weight of a colorless photoinitiator having an absorption maximum in the wavelength range of λ=300 to 400 nm; (C) 10% to 70% by weight of an alkyl and/or cycloalkyl acetate having 3 to 10 carbon atoms in the alkyl radical and/or in the cycloalkyl radical; (D) 10% to 70% by weight of an alkoxyalkyl, alkoxycycloalkyl, cycloalkoxyalkyl and/or cycloalkoxycycloalkyl acetate; (E) 0.01% to 5% by weight of a constituent that lowers the interfacial tension; (F) 0 to 50% by weight of an alkylaromatic having at least two alkyl radicals having 1 to 6 carbon atoms in the molecule; and (G) 0 to 50% by weight of an additive different from constituents (A) to (F); processes for preparing it, and its use as a spot blender in automotive refinishing, especially in spot repair, or for preparation thereof.

Claims (40)

1. A UV-A-curable, solvent-containing composition comprising

(A) 1% to 50% by weight of at least one UV A curable constituent selected from the group consisting of monomers (a1) comprising at least three UV A-curable reactive functional groups and at least one isocyanate-reactive functional group and mixtures (a2) of monomers (a21) that are free from isocyanate-reactive functional groups and comprise at least two UV-A-curable reactive functional groups, and monomers (a22) that comprise at least two UV A curable reactive functional groups and at least one isocyanate-reactive functional group;

(B) 0.01% to 10% by weight of at least one colorless or substantially colorless photoinitiator having at least one absorption wavelength maximum of 300 to 400 nanometers;

(C) 10% to 70% by weight of at least one alkyl and/or cycloalkyl acetate having 3 to 10 carbon atoms in the alkyl radical and/or in the cycloalkyl radical;

(D) 10 to 70% by weight of at least one alkoxyalkyl, alkoxycycloalkyl, cycloalkoxyalkyl and/or cycloalkoxycycloalkyl acetate;

(E) 0.001% to 5% by weight of at least one constituent that lowers the interfacial tension; and

(F) 0 to 50% by weight of at least one alkylaromatic having at least two alkyl radicals having 1 to 6 carbon atoms in the molecule.

2. The composition of claim 1 , wherein the monomer (a1) comprises at least four UV-A-curable reactive functional groups.

3. The composition of claim 2 , wherein the monomer (a1) comprises one isocyanate-reactive functional group.

4. The composition of claim 1 , wherein the monomer (a21) comprises at least three UV A-curable reactive functional groups.

5. The composition of claim 1 , wherein the monomer (a22) comprises one isocyanate-reactive functional group.

6. The composition of claim 4 , wherein the monomer (a21) comprises at least four UV A-curable reactive functional groups.

7. The composition of claim 1 , wherein the UV A curable reactive functional groups are acrylate groups.

8. The composition of claim 1 , wherein the isocyanate-reactive functional groups of monomers (a1) and (a22) are hydroxyl groups.

9. The composition of claim 1 , comprising (A) in an amount of 5% to 20% by weight.

10. The composition of claim 1 , comprising (B) in an amount of 0.05% to 5% by weight.

11. The composition of claim 1 , wherein (B) has at least one absorption wavelength maximum of 320 to 390 nanometers.

12. The composition of claim 1 , comprising (C) in an amount of 15% to 50% by weight.

13. The composition of claim 1 , comprising (D) in an amount of 15% to 50% by weight.

14. The composition of claim 1 , comprising (F) in an amount of 10 to 30% by weight.

15. The composition of claim 1 , comprising (E) in an amount of 0.005% to 2% by weight.

16. A method of manufacturing the UV A-curable, solvent-containing composition of claim 1 , comprising mixing (A) to (F) to produce a homogeneous mixture.

17. The method of claim 16 , wherein the method is carried out in the absence of actinic radiation.

18. A UV A-curable spot blender for automotive refinishing, comprising the UV-A-curable, solvent-containing composition of claim 1 .

19. The UV-A-curable spot blender of claim 18 , further comprising a refinish clearcoat material.

20. A UV-A-curable, solvent-containing composition comprising

(A) 1% to 50% by weight of at least one UV A curable constituent selected from the group consisting of monomers (a1) comprising at least three UV A-curable reactive functional groups and at least one isocyanate-reactive functional group and mixtures (a2) of monomers (a21) that are free from isocyanate-reactive functional groups and comprise at least two UV-A-curable reactive functional groups, and monomers (a22) that comprise at least two UV A curable reactive functional groups and at least one isocyanate-reactive functional group;

(B) 0.01% to 10% by weight of at least one colorless or substantially colorless photoinitiator having at least one absorption maximum in the wavelength range of λ=300 to 400 nm;

(C) 10% to 70% by weight of at least one alkyl and/or cycloalkyl acetate having 3 to 10 carbon atoms in the alkyl radical and/or in the cycloalkyl radical;

(D) 10% to 70% by weight of at least one alkoxyalkyl, alkoxycycloalkyl, cycloalkoxyalkyl and/or cycloalkoxycycloalkyl acetate;

(E) 0.001 to 5% by weight of at least one constituent that lowers the interfacial tension;

(F) 0 to 50% by weight of at least one alkylaromatic having at least two alkyl radicals having 1 to 6 carbon atoms in the molecule; and

(G) 0.01 to 2% by weight of at least one catalyst for the reaction between isocyanate groups and isocyanate-reactive functional groups.

21. The UV-A-curable, solvent-containing composition of claim 20 , wherein the at least one catalyst is selected from the group consisting of bismuth compounds and tin compounds.

22. A method of spot repairing paint finishes comprising

(A) applying a basecoat material to a substrate;

(B) applying a clearcoat material wet-on-wet to the basecoat film;

(C) applying the UV-A-curable, solvent-containing composition of claim 1 ; and

(D) curing the applied films.

23. The method of claim 22 , wherein the basecoat material comprises at least one platelet-shaped aluminum effect pigment, and the clearcoat material comprises is curable with UV-A radiation, or both thermally and with UV-A radiation.

Assignments (2)
CHANGE OF NAME Recorded Jan 19, 2012
From: LETTMANN, BERNHARD; REIZE, KLAUS-UDO; NIENHAUS, EGBERT
To: BASF COATINGS GMBH
Reel/Frame 027557/0925 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 22, 2007
From: LETTMANN, BERNHARD; REIZE, KLAUS-UDO; NIENHAUS, EGBERT
To: BASF COATINGS AKTIENGESELLSCHAFT
Reel/Frame 019730/0930 →
Priority Claims (1)
DE 10 2005 012 589 · Mar 18, 2005 · national
Continuity (1)
Related Publication 20080090935A1 · Apr 17, 2008