Method for producing a multicoat paint system

Patent metadata

Field	Value
Publication number	US-9868134-B2
Application number	US-201415027408-A
Country	US
Kind code	B2
Filing date	Nov 18, 2014
Priority date	Dec 18, 2013
Publication date	Jan 16, 2018
Grant date	Jan 16, 2018

Abstract

The present invention relates to a method for producing a multicoat paint system on a metallic substrate, in which a basecoat or a plurality of directly successive basecoats are produced directly on a metallic substrate coated with a cured electrocoat, a clearcoat is produced directly on the one basecoat or the uppermost of the plurality of basecoats, and then the one or more basecoats and the clearcoat are jointly cured, and wherein at least one basecoat material used for production of the basecoats comprises at least one aqueous dispersion comprising at least one copolymer (CP), said copolymer (CP) being preparable by initially charging an aqueous dispersion of at least one polyurethane, and then polymerizing a mixture of olefinically unsaturated monomers in the presence of the polyurethane from (i), in which a water-soluble initiator is used, the olefinically unsaturated monomers are metered in such that a concentration of 6.0% by weight, based on the total amount of olefinically unsaturated monomers used for polymerization, in the reaction solution is not exceeded over the entire reaction time, and the mixture of the olefinically unsaturated monomers comprises at least one polyolefinically unsaturated monomer, and comprises at least one linear hydroxy-functional reaction product (R) having an acid number less than 20 mg KOH/g, the preparation of which involves using at least one compound (v) containing two functional groups (v.1) and an aliphatic or araliphatic hydrocarbyl radical (v.2) which is arranged between the functional groups and has 12 to 70 carbon atoms.

First claim

The invention claimed is:

1. A method for producing a multicoat paint system (M) on a metallic substrate (S), said method comprising:
(1) producing a cured electrocoat (E.1) on the metallic substrate (S) by electrophoretic application of an electrocoat (e.1) to the substrate (S) and subsequent curing of the electrocoat (e.1),
(2) producing (2.1) a basecoat (B.2.1) or (2.2) a plurality of directly successive basecoats (B.2.2.x) directly on the cured electrocoat (E.1) by (2.1) applying an aqueous basecoat material (b.2.1) directly to the electrocoat (E.1) or (2.2) applying a plurality of basecoat materials (b.2.2.x) in direct succession to the electrocoat (E.1),
(3) producing a clearcoat (K) directly on (3.1) the basecoat (B.2.1) or (3.2) an uppermost basecoat (B.2.2.x) by applying a clearcoat material (k) directly to (3.1) the basecoat (B.2.1) or (3.2) the uppermost basecoat (B.2.2.x),
(4) jointly curing (4.1) the basecoat (B.2.1) and the clearcoat (K) or (4.2) the basecoats (B.2.2.x) and the clearcoat (K),
wherein the basecoat material (b.2.1) or at least one of the basecoat materials (b.2.2.x) comprises at least one aqueous dispersion comprising at least one copolymer (CP), said copolymer (CP) being preparable by
(i) initially charging an aqueous dispersion of at least one polyurethane, and then
(ii) polymerizing a mixture of olefinically unsaturated monomers in the presence of the polyurethane from (i),
in which
(a) a water-soluble initiator is used,
(b) the olefinically unsaturated monomers are metered so that a concentration of 6.0% by weight, based on the total amount of olefinically unsaturated monomers used for polymerization, in the reaction solution is not exceeded over the entire reaction time, and
(c) the mixture of the olefinically unsaturated monomers comprises at least one polyolefinically unsaturated monomer, and

comprises at least one linear hydroxy-functional reaction product (R) having an acid number less than 20 mg KOH/g, the preparation of which involves using at least one compound (v) containing two functional groups (v′0.1) and an aliphatic or araliphatic hydrocarbyl radical (v.2) which is arranged between the functional groups and has 12 to 70 carbon atoms;
wherein the at least one reaction product (R) is selected from the group consisting of
reaction products preparable by reaction of dimer fatty acids with at least one aliphatic dihydroxy-functional compound of the general structural formula (I):

where R is a C 3 to C 6 alkylene radical and n is correspondingly selected such that the compound of the formula (I) has a number-average molecular weight of 120 to 6000 g/mol, the dimer fatty acids and the compounds of the formula (U are used in a molar ratio of 0.7/2.3 to 1.6/1.7, and the resulting reaction product has a number-average molecular weight of 600 to 40000 g/mol and an acid number of less than 10 mg KOH/g,
reaction products preparable by reaction of dimer fatty acids with at least one dihydroxy-functional compound of the general structural formula (II):

where
R is a divalent organic radical comprising 2 to 10 carbon atoms,
R 1 and R 2 are each independently straight-chain or branched alkylene radicals having 2 to 10 carbon atoms,
X and Y are each independently O, S or NR 3 in which R 3 is hydrogen or an alkyl radical having 1 to 6 carbon atoms, and
m and n are correspondingly selected such that the compound of the formula (II) has a number-average molecular weight of 450 to 2200 g/mol,
where components (a) and (b) are used in a molar ratio of 0.7/2.3 to 1.6/1.7 and the resulting reaction product has a number-average molecular weight of 1200 to 5000 g/mol and an acid number of less than 10 mg KOH/g, and
reaction products preparable by reaction of dimer fatty acids with dimer diols, where the dimer fatty acids and dimer diols are used in a molar ratio of 0.7/2.3 to 1.6/1.7 and the resulting reaction product has a number-average molecular weight of 1200 to 5000 g/mol and an acid number of less than 10 mg KOH/g.

2. The method as claimed in claim 1 , wherein the mixture of olefinically unsaturated monomers used in (ii) comprises 0.1 to 6.0 mol % of polyolefinically unsaturated monomers.

3. The method as claimed in claim 1 , wherein the mixture of olefinically unsaturated monomers used in (ii) comprises allyl methacrylate, and no further polyolefinically unsaturated monomers are present.

4. The method as claimed in claim 1 , wherein the olefinically unsaturated monomers in (ii) (b) are metered in such that a concentration of 4.0% by weight, based on the total amount of olefinically unsaturated monomers used for polymerization, in the reaction solution is not exceeded over the entire reaction time.

5. The method as claimed in claim 1 , wherein the functional groups (v.1) of the at least one compound (v) are selected from the group consisting of hydroxcyl groups and carboxyl groups.

6. The method as claimed in claim 1 , wherein dimeric fatty acids and/or dimer diols are used as compound (v) in the preparation of the reaction product (R).

7. The method as claimed in claim 1 , wherein the reaction product (R) is preparable by reaction of at least one dimer fatty acid with at least one aliphatic, araliphatic or aromatic dihydroxy-functional compound having a number-average molecular weight of 120 to 6000 g/mol.

8. The method as claimed in claim 7 , wherein the aliphatic, araliphatic and/or aromatic dihydroxy-functional compound(s) used are at least one selected from the group consisting of polyether diols, polyester diols and dimer diols.

9. The method as claimed in claim 1 , wherein the basecoat material (b.2.1) or at least one, or all, of the basecoat materials (b.2.2.x) comprise(s) at least one hydroxyl-functional polymer other than (CP) and (R) as a binder, selected from the group consisting of polyurethanes, polyesters, polyacrylates and copolymers of these polymers and a melamine resin as a crosslinking agent.

10. The method as claimed in claim 1 , wherein the basecoat material (b.2.1) or at least one, or all, of the basecoat materials (b.2.2.x), comprise(s) at least one color pigment and/or effect pigment.

11. The method as claimed in claim 1 , wherein the basecoat material (b.2.1) or at least one of the basecoat materials (b.2.2.x) comprises a lamellar aluminum pigment or other metal effect pigment.

12. The method as claimed in claim 1 , wherein the basecoat material (b.2.1) or at least one, or all, of the basecoat materials (b.2.2.x), is/are one-component coating compositions.

13. The method as claimed in claim 1 , wherein the joint curing (4) is performed at temperatures of 100 to 250° C. for a period of 5 to 60 min.

14. The method as claimed in claim 1 , wherein (2.2) two basecoats (B.2.2.a) and (B2.2.z) are produced, for which the aqueous basecoat materials (b.2.2.a) and (b.2.2.z) used are identical and comprise effect pigments.

15. The method as claimed in claim 14 , wherein the basecoat material (b.2.2.a) is applied by electrostatic spray application, and the basecoat material (b.2.2.z) by pneumatic application.

16. The method as claimed in claim 1 , wherein (2.2) at least two basecoats are produced, the first basecoat (B.2.2.a) directly atop the electrocoat (E.1) comprising white pigments and black pigments, and the further basecoats (B.2.2.x) comprising effect pigments.

17. A multicoat paint syst

Assignees

• Basf Coatings Gmbh

Inventors

• Steinmetz Bernhard
• Krumm Holger
• Goh Stephanie Pei Yii
• Hoffmann Peter
• Reuter Hardy
• Jankowski Peggy
• Luhmann Nadia

Classifications

• C09D5/44

  for electrophoretic applications (processes for coating by electrophoresis C25D13/00) · CPC title

• B05D7/577 Primary

  some layers being coated "wet-on-wet", the others not · CPC title

• B05D7/14

  to metal, e.g. car bodies (involving a chemical reaction between the metal and the coating C23) · CPC title

• B05B5/00

  Electrostatic spraying apparatus; Spraying apparatus with means for charging the spray electrically; Apparatus for spraying liquids or other fluent materials by other electric means · CPC title

• B05D1/04 Primary

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