Curable aqueous polyurethane dispersions

• US 7,169,841 B2
• Filed: 06/26/2001
• Issued: 01/30/2007
• Est. Priority Date: 06/27/2000
• Status: Expired due to Fees

• Current Assignee: BASF AG (BASF SE)
• Original Assignee: BASF AG (BASF SE)
• Inventors: Bruchmann, Bernd, Schwalm, Reinhold, Beck, Erich, Schrof, Wolfgang, Meisenburg, Uwe, Voellinger, Frank
• Primary Examiner(s): Niland; Patrick D.
• Application Number:
  US10/311,307
• Publication Number:
  US 20030153673A1
• Time in Patent Office: 2,044 Days
• Field of Search: 524/507, 524/589, 524/590, 524/591, 524/839, 524/840, 525/455, 525/123, 525/131, 427/372.2, 427/385.5, 428/423.1
• US Class Current: 524/507
• CPC Class Codes: C08G 18/0823 containing carboxylate salt groups or groups forming them
• CPC Class Codes: C08G 18/7837 containing allophanate groups
• CPC Class Codes: C08G 18/8175 with esters of acrylic or alkylacrylic acid having only one group containing active hydrogen
• CPC Class Codes: C09D 175/16 having terminal carbon-to-carbon unsaturated bonds
• CPC Class Codes: Y10T 428/31551 Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]

Abstract

A curable aqueous polyurethane dispersion substantially comprises

• a) at least one compound having two free isocyanate groups, at least one allophanate group and at least one C═C double bond capable of free radical polymerization, a carbonyl group or an oxygen atom in the form of an ether function being bonded directly to the double bond,
• b) at least one compound having at least one group reactive toward isocyanate groups and having a C═C double bond capable of free-radical polymerization,
• c) if required, at least one compound having at least two groups reactive towards isocyanate groups and selected from hydroxyl, mercapto, primary and/or secondary amino groups,
• d) at least one compound having at least one group reactive towards isocyanate groups and having at least one acid group,
• e) at least one basic compound for neutralizing or partially neutralizing the acid groups of the compounds d),
  • and a thermal initiator and is used for coating substrates.

Claims

1. A curable aqueous polyurethane dispersion, comprising:

a) at least one compound having at least two free isocyanate groups, at least one allophanate group and at least one C═

C double bond capable of free radical polymerization, wherein a carbonyl group or an oxygen atom in the form of an ether function is bonded directly to the double bond,

b) at least one compound having at least one group reactive toward isocyanate groups and having a C═

C double bond capable of free-radical polymerization,

c) optionally at least one compound having at least two groups reactive toward isocyanate groups and selected from the group consisting of hydroxyl, mercapto, primary secondary amino groups, and combinations thereof,

d) at least one compound having at least one group reactive toward isocyanate groups and having at least one acid group,

e) at least one basic compound for neutralizing or partially neutralizing the acid groups of the compound d),

f) optionally at least one compound different from b), d) and e) and having only one group reactive toward isocyanate groups,

g) optionally at least one polyisocyanate different from a),

h) at least one thermal initiator,

i) optionally, one or more further additives selected from the group consisting of reactive diluents, photoinitiators and conventional coating additives, and

k) water.

2. The dispersion as claimed in claim 1, wherein the component a) is of formula I

OCN—

R¹R²—

C(O)—

R²—

R¹_nNCO 

 

(I)

where

n is an integer from 1 to 10,

R¹ is a divalent aliphatic or alicylic C₂- to C₂₀-hydrocarbon unit or an aromatic C₆- to C₂₀-hydrocarbon unit,

R² in each repeating unit may be —

NH—

or

3. The dispersion as claimed in claim 1, wherein the thermal initiator h) has a half-life at 60°

C. of at least one hour.

4. The dispersion as claimed in claim 1, wherein the component h) comprises at least one compound which has at least one group reactive toward isocyanate groups and is capable of liberating free radicals thermally even after reaction with a compound containing isocyanate groups.

5. The dispersion as claimed in claim 1, wherein the component h) comprises benzopinacol or a derivative thereof.

6. The dispersion as claimed in claim 1, wherein the component h) comprises an (arylsulfonyl) acetic acid alkyl ester.

7. The dispersion as claimed in claim 1, wherein the isocyanate groups of the compounds of component a) and, if present, g) are reacted to an extent of

from 5 to 98 mol % with groups of at least one compound of component b) which are reactive toward isocyanate groups,

from 0 to 70 mol % with groups of at least one compound of component c) which are reactive toward isocyanate groups,

from 2 to 10, mol % with groups of at least one compound of component d) which are reactive toward isocyanate groups.

8. A process for coating an article, comprising

i) coating an article with a dispersion as claimed in claim 1,

ii) removing volatile components of the dispersion for film formation under conditions under which the thermal initiator h) substantially forms no free radicals,

iii) optionally, exposing the film formed in step ii) to high-energy radiation to precure the film, and then, optionally, coating the article with the precured film, wherein the article coated with the precured film is mechanically processed or the surface of the precured film is brought into contact with another article, and

iv) subjecting the film to thermal final curing.

9. A coated article obtained by the process as claimed in claim 8.

10. The dispersion as claimed in claim 7 wherein the isocyanate groups of the compounds of component a) and, if present, g) are reacted to an extent of from 10 to 80 mol % with groups of at least one compound of component b).

11. The dispersion as claimed in claim 7, wherein the isocyanate groups of the compounds of component a) and, if present, g), are reacted to an extent of from 20 to 60 mol % with groups of at least one compound of component c).

12. The dispersion as claimed in claim 7, wherein the isocyanate groups of the compounds of component a) and, if present, g) are reacted to an extent of from 4 to 8 mol % with groups of at least one compound of component d).

13. A method comprising:

coating a substrate with the dispersion as claimed in claim 1.

14. The method of claim 13, wherein the substrate comprises metal, wood, paper, ceramic, glass, plastic, textile, leather, nonwoven or a mineral building material.

15. A method comprising

coating a surface with the dispersion as claimed in claim 1,

wherein the surface is an exterior coating.

16. The method of claim 15 wherein the surface is a surface of a building, a portion of a building, a road marking, a coating on a vehicle or a coating on an aircraft.

17. An automotive clear coat comprising the dispersion as claimed in claim 1.

18. A curable aqueous polyurethane dispersion, comprising:

a) at least one compound having

at least two free isocyanate groups,

at least one allophanate group, and

at least one C═

C double bond capable of free radical polymerization,

a carbonyl group or an oxygen atom in the form of an ether function directly bonded to the double bond,

b) at least one compound having at least one group reactive toward isocyanate groups and having a C═

C double bond capable of free-radical polymerization,

c) optionally at least one compound having at least two groups reactive toward isocyanate groups and selected from the group consisting of hydroxyl, mercapto, primary secondary amino groups, and combinations thereof,

d) at least one compound having at least one group reactive toward isocyanate groups and having at least one acid group,

e) at least one basic compound for neutralizing or partially neutralizing the acid groups of the compound d),

f) optionally at least one compound different from b), d) and e) and having only one group reactive toward isocyanate groups,

g) optionally at least one polyisocyanate different from a),

h) at least one thermal initiator,

i) optionally, one or more further additives selected from the group consisting of reactive diluents, photoinitiators and conventional coating additives, and

k) water.