Method for improving the adhesion of the intermediate layer in a multi-paint finish

• US 7,579,048 B2
• Filed: 03/03/2004
• Issued: 08/25/2009
• Est. Priority Date: 03/15/2003
• Status: Expired due to Fees

• Current Assignee: BASF Coatings AG (BASF SE)
• Original Assignee: Basf Coatings
• Inventors: Wegner, Egon, Schwarte, Stephan
• Primary Examiner(s): Lipman; Bernard
• Application Number:
  US10/549,055
• Publication Number:
  US 20060193989A1
• Time in Patent Office: 2,001 Days
• Field of Search: 524/839, 524/840, 525/124, 525/330.5, 427/402, 427/407.1
• US Class Current: 427/402
• CPC Class Codes: B05D 7/572 all layers being cured or baked together
• CPC Class Codes: B05D 7/577 some layers being coated "wet-on-wet", the others not
• CPC Class Codes: C08F 257/02 on to polymers of styrene or alkyl-substituted styrenes
• CPC Class Codes: C08F 265/04 on to polymers of esters
• CPC Class Codes: C08F 291/00 Macromolecular compounds obtained by polymerising monomers on to macromolecular compounds according to more than one of the groups C08F251/00 - C08F289/00
• CPC Class Codes: C08G 18/12 using two or more compounds having active hydrogen in the first polymerisation step
• CPC Class Codes: C08G 18/3275 containing two hydroxy groups
• CPC Class Codes: C08G 18/4233 derived from polymerised higher fatty acids or alcohols
• CPC Class Codes: C08G 18/6659 with compounds of group C08G18/34
• CPC Class Codes: C08L 2666/02 Organic macromolecular compounds, natural resins, waxes or and bituminous materials
• CPC Class Codes: C08L 51/003 grafted on to macromolecular compounds obtained by reactions only involving unsaturated carbon-to-carbon bonds C08L51/04, C08L51/06 take precedence
• CPC Class Codes: C09D 151/003 grafted on to macromolecular compounds obtained by reactions only involving unsaturated carbon-to-carbon bonds C09D151/04, C09D151/06 take precedence
• CPC Class Codes: C09D 175/04 Polyurethanes

Abstract

A process for improving the intercoat adhesion in a multicoat paint system utilizing a primer coat, an aqueous basecoat, and a clearcoat, where the multicoat paint system has been produced by means of a wet-on-wet technique. The clearcoat is produced using a pseudoplastic powder clearcoat slurry prepared by a secondary dispersion process or a melt emulsification process. The aqueous basecoat material used to produce the aqueous basecoat comprises a dispersed graft copolymer whose particles are composed of a hydrophobic core of copolymerized olefinically unsaturated monomers and of a hydrophilic shell which comprises a polyurethane, where said copolymer is prepared by free-radical (co)polymerization of the monomers in the presence of at least one polyurethane containing specially selected olefinically unsaturated groups.

Claims

1. A process for improving the intercoat adhesion in a multicoat paint system produced by means of an integrated wet-on-wet process comprising

(I) applying at least one primer material to the surface of a substrate, to form at least one primer film, and if desired drying the resulting primer film(s) 1, without fully curing it (them), or curing the primer film(s) 1 to give at least one primer coat 1,

(II) applying at least one aqueous basecoat material 2 to the outer surface of the primer film(s) 1 or primer coat(s) 1 and if desired drying the resulting aqueous basecoat film(s) 2 without fully curing it (them),

(III) applying at least one aqueous basecoat material 3 to the outer surface of the dried aqueous basecoat film(s) 2 and if desired drying the resulting aqueous basecoat film(s) 3 without fully curing it (them),

(IV) applying at least one pseudoplastic powder clearcoat slurry 4 prepared by means of at least one of

(α

) a secondary dispersion process of emulsifying an organic solution comprising binder and crossliniker to give an emulsion of the oil-in-water type, removing the organic solvent or solvents, and replacing some or all of the subtracted solvent volume by water, to give the powder clearcoat slurry comprising spherical dimensionally stable particles, or

(β

) a melt emulsification process in which at least one constituent of the powder clearcoat slurry is emulsified in the melt state, in an aqueous medium to form an aqueous emulsion of liquid particles and the emulsion is cooled to form an aqueous suspension of dimensionally stable particles,

 

to the outer surface of the dried aqueous basecoat film(s) 3 and optionally drying the resulting clearcoat film(s) 4, and

(V) jointly curing the clearcoat film(s) 4, the aqueous basecoat film(s) 3, and the aqueous basecoat film(s) 2 and also where appropriate the primer film(s), if uncured, 1 to give the multicoat paint system comprising at least one primer coat 1, at least one aqueous basecoat 2, at least one aqueous basecoat 3, and at least one clearcoat 4;

wherein the aqueous basecoat material(s) 2 employed in stage (II) comprise(s) as binder at least one dispersed graft copolymer (A/B) whose particles are composed of a hydrophobic core (A) of at least one copolymerized olefinically unsaturated monomer (a) and a hydrophilic shell (B) which comprises at least one polyurethane (b) and is prepared by subjecting the monomers (a) to free-radical (co)polymerization in the presence of at least one polyurethane (b) containing at least one olefinically unsaturated group selected from the group consisting of

lateral and terminal ethenylarylene groups;

lateral olefinically unsaturated groups attached to cycloaliphatic groups which constitute members of the main polymer chains;

lateral cycloolefinically unsaturated groups which constitute members of the main polymer chains;

terminal olefinically unsaturated groups attached to cycloaliphatic groups which constitute the end groups of the main polymer chains;

terminal cycloolefinically unsaturated groups which constitute the end groups of the main polymer chains; and

lateral and terminal olefinically unsaturated groups obtained by reacting polyurethanes with anhydrides of alpha,beta-unsaturated carboxylic acids and further wherein the aqueous basecoat material(s) 3 are different from the aqueous basecoat material(s) 2 and do not comprise the at least one dispersed graft copolymer (A/B) binder of the aqueous basecoat material(s) 2.

2. The process of claim 1, wherein the pseudoplastic powder clearcoat slurry 4 is prepared by a secondary dispersion process.

3. The process of claim 2, wherein the pseudoplastic powder clearcoat slurry 4 is free from organic solvents and external emulsifiers and the dimensionally stable spherical particles have an average size of from 0.8 to 20 μ

m and a maximum size of 30 μ

m.

4. The process of claim 1, wherein an ethenylarylene group of the general formula I is used:

CH₂═

C(R)-A- 

 

(I),

in which the variable A stands for a substituted or unsubstituted C₆-C₂₀ arylene radical and the variable R stands for at least one of a hydrogen atom, a halogen atom, a nitrile group, an unsubstituted alkyl, substituted alkyl, cycloalkyl, alkylcycloalkyl, cycloalkylalkyl, aryl, alkylaryl, cycloalkylaryl, arylalkyl and arylcycloalkyl radicals.

5. The process of claim 4, wherein the radical R stands for a hydrogen atom or a methyl group, in particular a methyl group.

6. The process of claim 1, wherein the arylene radical is 1,2-, 1,3- and/or 1,4-phenylene, in particular 1,3-phenylene.

7. The process of claim 1, wherein the ethenylarylene group is connected to the main chain of the polyurethane (b) by way of a divalent or trivalent linking radical containing at least one urethane and/or urea group.

8. The process of claim 7, wherein the linking radical contains at least one of the divalent or trivalent groups of the general formulae IIa to IIc

—

X—

NH—

C(O)—

O—

 

 

(IIa),

—

X—

NH—

C(O)—

NH—

 

 

(IIb) or

—

X—

NH—

C(O)—

N<

 

 

(IIc),

in which X is a divalent organic radical.

9. The process of claim 1, wherein the olefinically unsaturated groups attached to the cycloaliphatic groups are selected from the group consisting of (meth)acrylate, ethacrylate, crotonate, cinnamate, vinyl ether, vinyl ester, vinyl, dicyclopentadienyl, norbornenyl, isoprenyl, isopropenyl, allyl and butenyl groups and mixtures thereof dicyclopentadienyl ether, norbomenyl ether, isoprenyl ether, isopropenyl ether, allyl ether and butenyl ether groups and mixtures thereof and dicyclopentadienyl ester, norbornenyl ester, isoprenyl ester, isopropenyl ester, allyl ester and butenyl ester groups and mixtures thereof.

10. The process of claim 9, wherein the olefinically unsaturated groups are vinyl groups.

11. The process of claim 1, wherein the cycloaliphatic groups are derived from cycloaliphatics having from 4 to 12 carbon atoms in the molecule and the cycloolefinic groups are derived from cycloolefins having from 4 to 12 carbon atoms in the molecule.

12. The process of claim 11, wherein the cycloaliphatic groups are derived from acompounds selected from the group consisting of cyclobutane, cyclopentane, cyclohexane, cycloheptane, cyclooctane, norbomane, bicyclo[2.2.2]octane, decalin, hydroindane, dicyclopentene, tricyclodecane and adamantane, and the cycloolefinic groups from cyclopentene, cyclohexene, cycloheptene, cyclooctene, norbomene, bicyclo[2.2.2]octene and dicyclopentene.

13. The process of claim 1, wherein the anhydrides of alpha, beta-unsaturated carboxylic acids are selected from the group consisting of acrylic, methacrylic, ethacrylic, and cinnamic anhydride.

14. The process of claim 13, wherein methacrylic anhydride is used.