Varnish and its use for producing varnish coatings and color-and/or effect-producing multi-layer coatings

• US 6,822,044 B1
• Filed: 01/11/2002
• Issued: 11/23/2004
• Est. Priority Date: 07/02/1999
• Status: Expired due to Fees

• Current Assignee: BASF Coatings AG (BASF SE)
• Original Assignee: BASF Coatings AG (BASF SE)
• Inventors: Bremser, Wolfgang
• Primary Examiner(s): Harlan, Robert D.
• Application Number:
  US10/018,352
• Time in Patent Office: 1,047 Days
• Field of Search: 525/64, 525/273, 525/397, 526/204, 526/292.3, 524/458, 524/500, 524/543, 524/555, 524/558, 524/549, 524/557, 524/515, 524/502, 428/423.1, 428/474.4, 428/480, 428/500
• US Class Current: 525/64
• CPC Class Codes: B05D 7/532 the two layers being cured or baked together, i.e. wet on wet
• CPC Class Codes: B05D 7/534 the first layer being let to dry at least partially before applying the second layer B05D7/538 takes precedence
• CPC Class Codes: B05D 7/574 at least some layers being let to dry at least partially before applying the next layer B05D7/577 takes precedence
• CPC Class Codes: B05D 7/577 some layers being coated "wet-on-wet", the others not
• CPC Class Codes: C08L 2666/14 Macromolecular compounds according to C08L59/00 - C08L87/00; Derivatives thereof
• CPC Class Codes: C08L 61/20 Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen with aminophenols C08L61/04
• CPC Class Codes: C09D 133/062 Copolymers with monomers not covered by C09D133/06

Abstract

The use of a copolymer (A) preparable by free-radical polymerization of

a) at least one olefinically unsaturated monomer and

b) at least one olefinically unsaturated monomer different than the olefinically unsaturated monomer (a) and of the general formula I

R¹R²C═CR³R⁴  (I)

 in which the radicals R¹, R², R³ and R⁴ each independently of one another are hydrogen atoms or substituted or unsubstituted alkyl, cycloalkyl, alkylcycloalkyl, cycloalkylalkyl, aryl, alkylaryl, cycloalkylaryl, arylalkyl or arylcycloalkyl radicals, with the proviso that at least two of the variables R¹, R², R³ and are substituted or unsubstituted aryl, arylalkyl or arylcycloalkyl radicals, especially substituted or unsubstituted aryl radicals; in an aqueous medium, in a clearcoat material used to produce clearcoats KL and multicoat color and/or effect coating systems ML.

Claims

1. A copolymer (A) prepared by free-radical polymerization of

a) at least one olefinically unsaturated monomer and

b) at least one olefinically unsaturated monomer different than the olefinically unsaturated monomer (a) and of the general formula I

3. The copolymer of claim 1, wherein the copolymer (A) is obtained by (i) subjecting at least one monomer (a) and at least one monomer (b) to free-radical polymerization in an aqueous medium to provide a reaction product, and then (ii) reacting the resultant reaction product with at least one further monomer (a) under free radical conditions.

4. The copolymer of claim 1, wherein the aryl radicals R¹, R², R³ and/or R⁴ of the compound (b) comprise phenyl or naphthyl radicals.

5. The copolymer of claim 4, wherein the substituents in radicals R¹, R² R³ and/or R⁴ of the compound (b) are electron-donating or electron-withdrawing atoms or organic radicals.

6. The copolymer of claim 1, wherein monomers (a) comprise at least one monomer selected from the group of

a1) (meth)acrylic esters which are essentially free from acid groups;

a2) monomers which carry per molecule at least one hydroxyl group, amino group, alkoxymethylamino group or imino group and are essentially free from acid groups;

a3) monomers which carry per molecule at least one acid group which can be converted to the corresponding acid anion group;

a4) vinyl esters of alpha-branched monocarboxylic acids having 5 to 18 carbon atoms in the molecule;

a5) reaction products of acrylic acid and/or methacrylic acid with the glycidyl ester of an alpha-branched monocarboxylic acid having 5 to 18 carbon atoms per molecule;

a6) cyclic and/or acyclic olefins;

a7) (meth)acrylamides;

a8) monomers containing epoxide groups;

a9) vinylaromatic hydrocarbons;

a10) nitrites;

a11) vinyl compounds;

a12) allyl compounds;

a13) polysiloxane macromonomers having a number-average molecular weight Mn of from 1000 to 40,000 and having on average from 0.5 to 2.5 ethylenically unsaturated double bonds per molecule; and

/or

a14) acryloxysilane-containing vinyl monomers, prepared by reacting hydroxyl-functional silanes with epichlorohydrin and then reacting the reaction product with (meth)acrylic acid and/or hydroxyalkyl and/or hydroxycycloalkyl esters of (meth)acrylic acid (monomers a2), and mixtures thereof.

8. The copolymer of claim 4, wherein the aryl radicals R¹, R², R³ and/or R⁴ of the compound (b) comprise phenyl radicals.

9. The copolymer of claim 5, wherein one or more of the substituents in radicals R¹, R², R³ and/or R⁴ of the compound (b) comprise at least one group selected from halogen atoms, nitrile, nitro, partially or fully halogenated alkyl, cycloalkyl, alkylcycloalkyl, cycloalkylalkyl, aryl, alkylaryl, cycloalkylaryl, arylalkyl and arylcycloalkyl radicals;

aryloxy, alkyloxy and cycloalkyloxy radicals;

arylthio, alkylthio and cycloalkylthio radicals;

hydroxyl groups and/or primary, secondary and/or tertiary amino groups, and mixtures thereof.

10. A clearcoat coating composition comprising the copolymer of claim 1.

2. A clearcoat material comprising

(A) a binder comprising at least one copolymer prepared by free-radical polymerization of

a) at least one olefinically unsaturated monomer and

b) at least one olefinically unsaturated monomer different than the olefinically unsaturated monomer (a) and of the general formula I

7. The clearcoat material of claim 2, wherein the clearcoat material further comprises at least one of the following constituents:

A) at least one binder different than the copolymer (A) and containing at least one functional group (afg) which is able to undergo thermal crosslinking reactions with complementary functional groups (bfg) in the crosslinking agent (B)

C) at least one constituent which is crosslinkable with actinic radiation,

D) at least one photoinitiator,

E) at least one thermal crosslinking initiator,

F) at least one reactive diluent curable thermally and/or with actinic radiation,

G) at least one coatings additive, and/or H) at least one organic solvent.