DE102010015683A1 - Coating agent based on aprotic solvents, useful e.g. as clear coat for automotive repair lacquering, comprises at least one oligomeric and/or polymeric hydroxyl group-containing compound (A) and at least one compound (B) - Google Patents

Abstract

Coating agent based on aprotic solvents comprises at least one oligomeric and/or polymeric hydroxyl group-containing compound (A) and at least one compound (B) with isocyanate groups and at least one silane group (I). The isocyanate groups and silane groups comprising compound (B) comprises uretdione group and the compound (B) is prepared from a linear aliphatic diisocyanate. Coating agent based on aprotic solvents comprises at least one oligomeric and/or polymeric hydroxyl group-containing compound (A) and at least one compound (B) with isocyanate groups and at least one silane group of formula (-X-Si-(R 2>) xG 3-x) (I). The isocyanate groups and silane groups comprising compound (B) comprises uretdione group and compound (B) is prepared from a linear aliphatic diisocyanate. G : hydrolyzable group, preferably OR 1>; R 1>H, alkyl or cycloalkyl, preferably C 2H 5or CH 3, where carbon chain is interrupted by nonadjacent O, S or NRa; R 2>alkyl, cycloalkyl, aryl or aralkyl, preferably 1-6C alkyl, where carbon chain is interrupted by nonadjacent O, S or NRa; Ra : alkyl, cycloalkyl, aryl or aralkyl; X : optionally branched 1-20C alkylene or 1-20C cycloalkylene, preferably 1-4C alkylene; and x : 0-2, preferably 0. Independent claims is also included for (1) a multi-stage coating process comprising applying a pigmented basecoat and then a layer of the coating agent on an optionally precoated substrate; and (2) applying the multi-stage coating process for automotive repair lacquering and for coating of plastic substrates.

Description

The present invention relates to coating compositions based on aprotic solvents, comprising at least one oligomeric and / or polymeric hydroxyl-containing compound (A) and at least one compound (B) with isocyanate groups and with silane groups.

Such coating compositions are for example from the WO 08/74491 . WO 08/74490 and the WO 08/74489 known. The compound (B) containing isocyanate groups and silane groups used in these coating compositions is based on known isocyanates, preferably on the biuret dimers and isocyanurate trimers of diisocyanates, in particular of hexamethylene diisocyanate. These coating agents of WO 08/074489 Compared with conventional polyurethane coating compositions have the advantage of a significantly improved scratch resistance at the same time good weather resistance. The coating compositions described therein are used in particular in automotive OEM finishing, although the use in automotive refinishing is also described. A disadvantage of these coating compositions, however, is that a reduction in the proportion of solvent, ie an increase in the non-volatile content, of the coating agent is associated with a deterioration in the flow properties and thus with a significant deterioration in the optical quality of the resulting coatings.

However, coating agents used for the automotive repair sector are affected by legal emission guidelines (eg 31st Bundesimmisionschutzverordnung). The current European directive requires a VOC ("volatile organic content") of 420 g / l for clearcoat systems, which results in non-volatile amounts of about 60% by weight, depending on the density of the system used. The problem with the development of systems with a high nonvolatile content is that the viscosity usually increases and thus the flowability of the system is lowered, which has an adverse effect on the course or topcoat level. To counteract this, the non-volatile portion must be raised at a constant viscosity. This is generally achieved by reducing the viscosity of the hardener and / or the binder. However, this is often associated with poorer physical film formation and results in longer drying times. Especially for coating compositions which are used in the field of automotive refinish, this condition is unfavorable, since the coating compositions used in the field of refinishing come up with long reaction times anyway.

From the US-A-5,691,439 coating compositions are known which contain not only hydroxyl-containing binders (A) as crosslinkers compounds (B) with isocyanate groups, it being essential to the invention that the compounds (B) also have allophanate groups for lowering the surface energy, silane groups or siloxane groups and transparent coatings to achieve so that coatings with improved surface properties are obtained. However, there is no indication in this document as to how the solvent content of the coating composition can be lowered and, nevertheless, good curing rates are ensured even under the conditions of automotive refinishing.

Furthermore, in the EP-A-1 273 640 A 2K coating composition containing a polyol component and a crosslinker component consisting of aliphatic and / or cycloaliphatic polyisocyanates or the polyisocyanates derived therefrom by polymerization, allophanate, biuret or urethane formation, wherein 0.1 to 95 mol% of the originally free existing isocyanate groups are reacted with bisalkoxysilylamine. These coating compositions can be used for the production of clearcoats or topcoats in the automotive sector and have, after their complete hardening, good scratch resistance combined with good resistance to environmental influences. However, this document does not contain any information on how the solvent content of the coating composition can be lowered, while still ensuring good curing rates under the conditions of automotive refinishing and that the surface properties of the resulting coatings are not impaired.

In the WO 2001/98393 describes 2K coating compositions containing a polyol as a binder component and as a crosslinking component, a polyisocyanate which is functionalized in low proportions with alkoxysilylamines, preferably with bisalkoxysilylamines. These coating compositions are used in particular as primers and optimized for adhesion to metallic substrates, preferably on aluminum substrates.

Finally, from the EP-A-1 426 393 low-monomer, uretdione group-containing polyisocyanates, which also have the advantage that they have improved compared to the previously used uretdiones Rückspaltstabilität. This improved cleavage stability is achieved by dimerizing the uretdiones at temperatures of <= 40 ° C in the presence of trialkylphosphines, and then the trialkylphosphines are separated off. The uretdiones are used for example as a hardener in coating compositions. However, this document lacks information on how the surface properties of the resulting coatings can be influenced as well as information on how a good curing can be ensured even under the conditions of refinishing.

task

The object of the present invention was therefore to provide coating compositions, in particular for automotive refinishing, which ensure good curing even under the conditions of refinishing, have a high solids content and thus the lowest possible solvent content, show a good course or topcoat level and lead to coatings with good surface properties.

To assess the overall visual impression, the measurement of the surface profile of the applied, baked-on coating films by means of the Wavescan method was used, which allows to measure the visible profile of paint film surfaces. For this purpose, the intensity of the reflection ("waviness") was measured by means of the device "Wave Scan" from Byk-Gardner, wherein 1250 measuring points were recorded over a distance of 10 cm. The reflection is measured by the meter in long wave ("long wave"), i. H. the variance of the light intensity for structures in the range of 0.6 mm to 10 mm and in short waviness, ie. H. divided the variance of the light intensity for structures in the range of 0.1 mm to 0.6 mm. In particular, low long-wave measurements of the resulting coatings at the lowest possible layer thicknesses are decisive for a good visual impression.

Furthermore, coating compositions should be made available which lead to a highly weather-stable network and at the same time ensure high acid resistance. In addition, the coating compositions should lead to coatings which are highly scratch-resistant and in particular have a high gloss retention after scratching. Furthermore, the coatings and finishes, especially the clearcoats, should also be able to be produced in layer thicknesses> 40 μm without stress cracks occurring. In addition, the coating compositions should meet the requirements usually imposed on the clearcoat film in automotive OEM finishes and automotive refinish.

Finally, the new coating compositions should be simple and very easy to produce reproducible and prepare during the paint application no environmental problems.

Solution of the task

• (i) die Isocyanatgruppen und Silangruppen enthaltende Verbindung (B) Uretdiongruppen aufweist und
• (ii) die Verbindung (B) aus einem linearen, aliphatischen Diisocyanat (DI) hergestellt worden ist.

In the light of the abovementioned problem, coating compositions based on aprotic solvents were found, comprising at least one oligomeric and / or polymeric hydroxyl group-containing compound (A) and at least one compound (B) with isocyanate groups and with at least one silane group of the formula (I) -X-Si-R " _x G _3-x (I) With
G = identical or different hydrolyzable groups, in particular G = alkoxy group (OR '),
R '= hydrogen, alkyl or cycloalkyl, where the carbon chain may be interrupted by nonadjacent oxygen, sulfur or NRa groups, where R a = alkyl, cycloalkyl, aryl or aralkyl, preferably R' = ethyl and / or methyl,
X = organic radical, in particular linear and / or branched alkylene or cycloalkylene radical having 1 to 20 carbon atoms, very particularly preferably X = alkylene radical having 1 to 4 carbon atoms,
R '' = alkyl, cycloalkyl, aryl, or aralkyl, wherein the carbon chain may be interrupted by non-adjacent oxygen, sulfur or NRa groups, with Ra = alkyl, cycloalkyl, aryl or aralkyl, preferably R "= alkyl radical, in particular with 1 to 6 C atoms,
x = 0 to 2, preferably 0 to 1, more preferably x = 0
characterized in that

• (i) the isocyanate group and silane group-containing compound (B) has uretdione groups, and
• (ii) the compound (B) has been prepared from a linear aliphatic diisocyanate (DI).

The present invention also relates to multistage coating processes using these coating compositions and to the use of the coating compositions as a clearcoat or application of the coating process for the coating of automotive components and / or plastic substrates and automotive refinishing.

In view of the prior art, it was surprising and unforeseeable for the person skilled in the art that the objects on which the present invention was based could be achieved with the aid of the coating compositions according to the invention.

Thus, it is particularly surprising that the coating compositions according to the invention ensure good curing even under the conditions of refinishing, have a high solids content and thus the lowest possible solvent content, show good flow or topcoat level and lead to coatings with good surface properties. Thus, the resulting coatings have, in particular, the low long-wave measurement values, which are important for a good visual impression, with the lowest possible layer thicknesses.

Furthermore, the coating agents lead to a highly weather-resistant network and at the same time ensure high acid resistance. In addition, the coating compositions lead to coatings that are highly scratch resistant and in particular have a high gloss retention after scratching. Furthermore, the coatings and coatings, especially the clearcoats, even in layer thicknesses> 40 microns can be produced without causing stress cracks. In addition, the coating compositions meet the requirements usually imposed on the clearcoat film in automotive OEM finishes and automotive refinish.

Finally, the new coating compositions are simple and very reproducible to produce and prepare during the application of paint no environmental problems.

Description of the invention

The coating compositions of the invention

In particular, the coating compositions according to the invention are thermally curable coating compositions, ie preferably coating compositions which are essentially free of radiation-curable unsaturated compounds, in particular completely free of radiation-curable unsaturated compounds.

The isocyanate group-containing compounds (B)

As component (B) the coating compositions according to the invention contain one or more compounds with free, d. H. unblocked, and / or blocked isocyanate groups. The coating compositions according to the invention preferably contain compounds (B) with free isocyanate groups. However, the free isocyanate groups of the isocyanate-containing compounds B can also be used in blocked form. This is preferably the case when the coating compositions according to the invention are used as one-component systems.

It is essential to the invention that the isocyanate group-containing compound used as component (B) in the coating composition has been prepared from at least one linear aliphatic diisocyanate (DI). This ensures that the resulting compounds (B) can be used both in the form of solids-rich solutions having a solids content of more than 70% by weight, in particular at least 75% by weight, in the coating compositions according to the invention and at the same time also the surface properties, such as especially the course, the resulting coatings are very good.

The isocyanate group-containing compound used as component (B) in the coating composition is preferably composed of at least one linear, aliphatic diisocyanate (DI) having 3 to 12 C atoms, in particular having 4 to 10 C atoms and very particularly having 5 to 6 C atoms been prepared.

Examples of the linear aliphatic diisocyanates (DI) which are suitable for the preparation of component (B) are butane diisocyanate, pentane diisocyanate, hexane diisocyanate, heptane diisocyanate, octane diisocyanate, nonane diisocyanate, decane diisocyanate, undecane diisocyanate, dodecane diisocyanate and, in particular, hexane diisocyanate.

Furthermore, it is essential to the invention that isocyanate-group-containing compound (B) additionally contains uretdione groups in addition to the free and / or blocked isocyanate groups. By using isocyanate-containing compounds containing uretdione groups, in contrast to the use of isocyanurates and, in contrast to the use of biurets and / or allophanates of the same diisocyanates, coatings with significantly better surface properties, in particular with lower long-wave values, are obtained. The long-wave values of the applied baked-on coating films are measured by means of the wavescan method, which makes it possible to measure the visible profile of coating film surfaces. For this purpose, the intensity of the reflection ("waviness") was measured by means of the device "Wave Scan" from Byk-Gardner, wherein 1250 measuring points were recorded over a distance of 10 cm. The reflectance becomes long-wave, ie the variance of the light intensity for structures in the range of 0.6 mm to 10 mm and in short waviness (short wave), ie the variance of the light intensity for structures in the range of 0.1 mm to 0.6 mm, divided.

The compound (B) has therefore preferably been prepared from a polyisocyanate (PI) having a uretdione group content of> 50 mol%, preferably more than 50 to 90 mol%, particularly preferably 65 to 80 mol%, in each case based on the entirety of by the isocyanate oligomerization of the linear aliphatic diisocyanate (DI) resulting structure types. For the preparation of component (B) suitable uretdiones are, for example, in the EP-A-1 426 393 , Page 2, paragraph [0012], to page 4, paragraph [0030] described.

The isocyanate group-containing compound used as component (B) in the coating composition additionally contains, in addition to the free and / or blocked isocyanate groups and in addition to the uretdione groups, at least one silane group of the formula (I) -X-Si-R " _x G _3-x (I) With
G = identical or different hydrolyzable groups, in particular G = alkoxy group (OR '),
R '= hydrogen, alkyl or cycloalkyl, where the carbon chain may be interrupted by nonadjacent oxygen, sulfur or NRa groups, where R a = alkyl, cycloalkyl, aryl or aralkyl, preferably R' = ethyl and / or methyl,
X = organic radical, in particular linear and / or branched alkylene or cycloalkylene radical having 1 to 20 carbon atoms, very particularly preferably X = alkylene radical having 1 to 4 carbon atoms,
R '' = alkyl, cycloalkyl, aryl, or aralkyl, wherein the carbon chain may be interrupted by non-adjacent oxygen, sulfur or NRa groups, with Ra = alkyl, cycloalkyl, aryl or aralkyl, preferably R "= alkyl radical, in particular with 1 to 6 C atoms,
x = 0 to 2, preferably 0 to 1, more preferably x = 0.

The coating composition preferably comprises at least one isocyanate group-containing compound (B) which, in addition to the free and / or blocked isocyanate groups and in addition to the uretdione groups, also contains at least one structural unit (II) of the formula (II) -NR- (X-SiR " _x (OR ') _3-x ) (II), and at least one structural unit (III) of the formula (III) -N (X-SiR " _x (OR ') _3-x ) _n (X'-SiR" _y (OR') _3-y ) _m (III) contains, where
R = hydrogen, alkyl, cycloalkyl, aryl or aralkyl, where the carbon chain may be interrupted by nonadjacent oxygen, sulfur or NRa groups, where R a = alkyl, cycloalkyl, aryl or aralkyl,
R '= hydrogen, alkyl or cycloalkyl, where the carbon chain may be interrupted by nonadjacent oxygen, sulfur or NRa groups, where R a = alkyl, cycloalkyl, aryl or aralkyl, preferably R' = ethyl and / or methyl,
X, X '= linear and / or branched alkylene or cycloalkylene radical having 1 to 20 carbon atoms, preferably X, X' = alkylene radical having 1 to 4 carbon atoms,
R '' = alkyl, cycloalkyl, aryl, or aralkyl, wherein the carbon chain may be interrupted by non-adjacent oxygen, sulfur or NRa groups, with Ra = alkyl, cycloalkyl, aryl or aralkyl, preferably R "= alkyl radical, in particular with 1 to 6 C atoms,
n = 0 to 2, m = 0 to 2, m + n = 2, and x, y = 0 to 2
is.

The respective preferred alkoxy radicals (OR ') may be identical or different, but it is crucial for the structure of the radicals how they influence the reactivity of the hydrolyzable silane groups. R 'is preferably an alkyl radical, in particular having 1 to 6 C atoms. Particular preference is given to radicals R 'which increase the reactivity of the silane groups, ie represent good leaving groups. In this respect, a methoxy radical is preferred over an ethoxy radical and this again relative to a propoxy radical. Therefore, R 'is preferably ethyl and / or methyl, in particular methyl.

Furthermore, the reactivity of organofunctional silanes can also be significantly influenced by the length of the spacers X, X 'between silane functionality and organic functional group which serves to react with the modifying constituent. Examples include the "alpha" silanes called, which are available from the company Wacker, and in which a methylene group is in place of the present in "gamma" silanes propylene group between Si atom and functional group.

The isocyanate group-containing compounds (B) functionalized with structural units (II) and (III) are particularly preferably prepared by reacting the uretdione-containing polyisocyanates (PI) - which have been prepared by oligomerizing the linear aliphatic diisocyanates (DI) - with at least one Compound of the formula (IIa) H-NR- (X-SiR " _x (OR ') _3-x ) (IIa), and with at least one compound of the formula (IIIa) HN (X-SiR " _x (OR ') _3-x ) _n (X'-SiR" _y (OR') _3-y ) _m (IIIa) obtained, wherein the substituents have the abovementioned meaning.

Preferred compounds (IIIa) according to the invention are bis (2-ethyltrimethoxysilyl) amine, bis (3-propyltrimethoxysilyl) amine, bis (4-butyltrimethoxysilyl) amine, bis (2-ethyltriethoxysilyl) amine, bis (3-propyltriethoxysilyl) amine and / or bis (4-butyltriethoxysilyl) amine. Very particular preference is given to bis (3-propyltrimethoxysilyl) amine. Such aminosilanes are available for example under the brand name ^® from DYNASILAN. DEGUSSA or Silquest ^® from. OSI.

Preferred compounds (IIa) according to the invention are aminoalkyltrialkoxysilanes, such as preferably 2-aminoethyltrimethoxysilane, 2-aminoethyltriethoxysilane, 3-aminopropyltrimethoxysilane, 3-aminopropyltriethoxysilane, 4-aminobutyltrimethoxysilane, 4-aminobutyltriethoxysilane. Particularly preferred compounds (Ia) are N- (2- (trimethoxysilyl) ethyl) alkylamines, N- (3- (trimethoxysilyl) propyl) alkylamines, N- (4- (trimethoxysilyl) butyl) alkylamines, N- (2- (triethoxysilyl ) ethyl) alkylamines, N- (3- (triethoxysilyl) propyl) alkylamines and / or N- (4- (triethoxysilyl) butyl) alkylamines. Very particularly preferred is N- (3- (trimethoxysilyl) propyl) butylamine. Such aminosilanes are available for example under the brand name ^® from DYNASILAN. DEGUSSA or Silquest ^® from. OSI.

It is preferred that the isocyanate group-containing compound (B) contain 2.5 and 90 mol%, especially 5 to 85 mol%, and more preferably 7.5 to 80 mol%, of at least one structural unit (II) of the formula (II ) and 2.5 and 90 mol%, in particular 5 to 85 mol%, and very particularly 7.5 to 80 mol%, of at least one structural unit (III) of the formula (III), in each case based on the entirety of Structural units (II) and (III).

It is particularly preferred that the total proportion of the isocyanate groups in the polyisocyanate (PI) reacted to the structural units (II) and / or (III) is between 5 and 95 mol%, preferably between 10 and 85 mol% and particularly preferably between 15 and 70 mol% lies.

Very particularly preferred isocyanate group-containing compounds (B) are reaction products of the uretdione of hexamethylene-1,6-diisocyanate with bis (3-propyltrimethoxysilyl) amine and N- (3- (trimethoxysilyl) propyl) butylamine.

The solids content of the polyisocyanate hardener (B) used according to the invention is advantageously more than 70% by weight, preferably at least 75% by weight.

The hydroxyl-containing compound (A)

The hydroxyl-containing compound (A) used is at least one oligomeric and / or polymeric polyol.

The preferred oligomeric and / or polymeric polyols (A) have mass-average molecular weights Mw> 500 daltons, measured by gel permeation chromatography (GPC) against a polystyrene standard, preferably between 800 and 100,000 daltons, in particular between 1,000 and 50,000 daltons.

Particular preference is given to polyester polyols, polyurethane polyols, polysiloxane polyols, polyacrylate polyols and / or polymethacrylate polyols and their copolymers, referred to below as polyacrylate polyols.

The polyols preferably have an OH number of 30 to 400 mg KOH / g, in particular between 100 and 300 KOH / g. The hydroxyl number (OH number) indicates how many mg of potassium hydroxide are equivalent to the amount of acetic acid bound by 1 g of substance in the acetylation. The sample is boiled in the determination with acetic anhydride-pyridine and the resulting acid is titrated with potassium hydroxide solution ( DIN 53240-2 ).

The glass transition temperatures, measured by DSC measurements after DIN-EN-ISO 11357-2 , the polyols are preferably between -150 and 100 ° C, more preferably between -120 ° C and 80 ° C.

Suitable polyester polyols are, for example, in EP-A-0 994 117 and EP-A-1 273 640 described. Polyurethane polyols are preferably prepared by reacting polyester polyol prepolymers with suitable di- or polyisocyanates and are described, for example, in EP-A-1 273 640. Suitable polysiloxane polyols are for example in the WO-A-01/09260 described, wherein the polysiloxane polyols listed there may be used preferably in combination with other polyols, especially those having higher glass transition temperatures.

The poly (meth) acrylate polyols very particularly preferred according to the invention are generally copolymers and preferably have mass-average molecular weights Mw between 1000 and 20,000 daltons, in particular between 1,500 and 10,000 daltons, in each case measured by gel permeation chromatography (GPC) against a polystyrene standard.

The glass transition temperature of the copolymers is generally between -100 and 100 ° C, in particular between -50 and 80 ° C (measured by DSC measurements after DIN-EN-ISO 11357-2 ).

The poly (meth) acrylate polyols preferably have an OH number of 60 to 250 mg KOH / g, in particular between 70 and 200 KOH / g, and an acid number between 0 and 30 mg KOH / g.

The hydroxyl number (OH number) indicates how many mg of potassium hydroxide are equivalent to the amount of acetic acid bound by 1 g of substance in the acetylation. The sample is boiled in the determination with acetic anhydride-pyridine and the resulting acid is titrated with potassium hydroxide solution ( DIN 53240-2 ). The acid number here indicates the number of mg of potassium hydroxide which is consumed to neutralize 1 g of the respective compound ( DIN EN ISO 2114 ).

Preferred hydroxyl-containing monomer building blocks are hydroxyalkyl acrylates and / or hydroxyalkyl methacrylates, in particular 2-hydroxyethyl acrylate, 2-hydroxyethyl methacrylate, 2-hydroxypropyl acrylate, 2-hydroxypropyl methacrylate, 3-hydroxypropyl acrylate, 3-hydroxypropyl methacrylate, 3-hydroxybutyl acrylate, 3-hydroxybutyl methacrylate and in particular 4-hydroxybutyl acrylate and or 4-hydroxybutyl methacrylate used.

Preferred other monomer building blocks for the poly (meth) acrylate polyols are preferably alkyl methacrylates and / or alkyl methacrylates, such as preferably ethyl acrylate, ethyl methacrylate, propyl acrylate, propyl methacrylate, isopropyl acrylate, isopropyl methacrylate, butyl acrylate, butyl methacrylate, isobutyl acrylate, isobutyl methacrylate, tert-butyl acrylate, tert-butyl methacrylate, amyl acrylate , Amyl methacrylate, hexyl acrylate, hexyl methacrylate, ethylhexyl acrylate, ethylhexyl methacrylate, 3,3,5-trimethylhexyl acrylate, 3,3,5-trimethylhexyl methacrylate, stearyl acrylate, stearyl methacrylate, lauryl acrylate or lauryl methacrylate, cycloalkyl acrylates and / or cycloalkyl methacrylates such as cyclopentyl acrylate, cyclopentyl methacrylate, isobornyl acrylate, isobornyl methacrylate or in particular cyclohexyl acrylate and / or cyclohexyl methacrylate.

As further monomer building blocks for the poly (meth) acrylate polyols it is possible to use vinylaromatic hydrocarbons, such as vinyltoluene, alpha-methylstyrene or, in particular, styrene, amides or nitriles of acrylic or methacrylic acid, vinyl esters or vinyl ethers, and in minor amounts, in particular acrylic and / or methacrylic acid ,

To further increase the solids content of the coating compositions of the invention and to further improve the surface quality (lower long-wave values), in particular in the case of a lower degree of silanization of the compound (B), in particular lactone-modified hydroxyl-containing oligomeric and / or polymeric compounds (A) are used. Particular preference is given to using ε-caprolactone-modified hydroxyl-containing oligomeric and / or polymeric compounds (A) and very particularly preferably ε-caprolactone-modified hydroxyl-containing polyacrylate polyols and / or ε-caprolactone-modified hydroxyl-containing polymethacrylate polyols.

The lactone-modified, in particular the ε-caprolactone-modified hydroxyl-containing oligomeric and / or polymeric compounds (A) can be prepared in a manner known to the skilled person by first preparing the hydroxyl-containing oligomeric and / or polymeric compounds and then using the lactone or ε-caprolactone be implemented. However, it is also possible first to react a part of the monomer building components, in particular a part of the hydroxyl-containing monomer building components, with the lactone or ε-caprolactone and then then to build up the lactone-modified or the ε-caprolactone-modified oligomer or polymer. Hydroxyl-containing compounds (A) modified with lactone or ε-caprolactone are also disclosed, for example, in US Pat US-A-4,546,046 , Column 4, lines 24 to column 7, line 6 described.

In a further embodiment of the invention, the hydroxyl group-containing compound A may, in addition to the hydroxyl groups, also have silane groups (I).

The combination of components (A) and (B) and other components of the coating composition

The proportions by weight of the polyol (A) and the polyisocyanate (B) are preferably selected such that the molar equivalent ratio of the unreacted isocyanate groups of the isocyanate-containing compounds (B) to the hydroxyl groups of the hydroxyl-containing compounds (A) is between 0.8: 1 and 1: 1.2, preferably between 0.9: 1 and 1.1: 1, more preferably between 0.95: 1 and 1.05: 1.

According to the invention, preference is given to using coating compositions which contain from 20 to 80% by weight, preferably from 30 to 70% by weight, based in each case on the solids content of the coating composition, at least one hydroxyl-containing polyacrylate (A) and / or at least one hydroxyl-containing polymethacrylate (A ) contain.

According to the invention, preference is given to using coating compositions which contain from 20 to 80% by weight, preferably from 30 to 70% by weight, based in each case on the solids content of the coating composition, of at least one isocyanate group-containing compound (B).

If it is one-component coating compositions, the isocyanate group-containing compounds (B) are selected whose free isocyanate groups are blocked with the blocking agents described above.

In the case of the 2-component (2K) coating compositions preferred according to the invention, shortly before the application of the coating composition, a coating component comprising the hydroxyl-containing compound (A) and further components described below, with a further coating component containing the isocyanate group-containing compound (B) and optionally further of the Components described below mixed in a conventional manner, wherein usually the paint component containing the compound (A), the catalyst and a part of the solvent.

In addition to the hydroxyl-containing component (A), the coating compositions according to the invention may optionally contain one or more hydroxyl-containing compounds (C) other than component (A). These compounds (C) preferably contain from 10 to 50% by weight, particularly preferably from 20 to 40% by weight, based on the nonvolatile fraction of the polyol component (A) + (C).

As hydroxyl-containing compound (C) both low molecular weight polyols and of the component (A) different, oligomeric and / or polymeric polyols are used.

As low molecular weight polyols, for example, diols, such as preferably ethylene glycol, neopentyl glycol, 1,2-propanediol, 2,2-dimethyl-1,3-propanediol, 1,4-butanediol, 1,3-butanediol, 1.5, - Pentanediol, 2,2,4-trimethyl-1,3-pentanediol, 1,6-hexanediol, 1,4-cyclohexanedimethanol and 1,2-cyclohexanedimethanol, as well as polyols, such as preferably trimethylolethane, trimethylolpropane, trimethylolhexane, 1,2,4 Butantriol, pentaerythritol and dipentaerythritol.

Preferably, such low molecular weight polyols are added in minor proportions of the polyol component (A).

As oligomeric and / or polymeric polyols (C), polyester polyols, polyurethane polyols and polysiloxane polyols are used, for example, if component (A) consists exclusively of polyacrylate polyols and / or polymethacrylate polyols.

Catalyst (D)

The coating compositions of the invention preferably contain at least one catalyst (D) for the crosslinking of the silane groups. Examples are metal complexes with chelating ligands based on zinc or aluminum, such as the z. B. in the WO05 / 03340 titanates or Lewis acids described, but care must be taken in the selection of the catalysts that the catalysts do not lead to yellowing of the coating agent. In addition, some known catalysts are less desirable for toxicological reasons.

It is therefore preferred that as catalyst (D), phosphorus-containing, in particular phosphorus-containing and nitrogen-containing catalysts are used. It is also possible to use mixtures of two or more different catalysts (D).

Examples of suitable phosphorus-containing catalysts (D) are substituted phosphonic diesters and diphosphonic diesters, preferably from the group consisting of acyclic phosphonic diesters, cyclic phosphonic diesters, acyclic diphosphonic diesters and cyclic diphosphonic diesters. Such catalysts are, for example, in the German patent application DE-A-10 2005 045 228 described.

In particular, however, substituted phosphoric monoesters and phosphoric diesters, preferably from the group consisting of acyclic phosphonic diesters and cyclic phosphonic diesters, more preferably amine adducts of the phosphoric acid mono- and di-esters, are used.

Very particular preference is given to using as catalysts (D) the corresponding amine-blocked phosphoric acid esters, in particular amine-blocked phosphoric acid ethylhexyl esters and amine-blocked phosphoric acid phenyl esters, very particularly preferably amine-blocked phosphoric acid bis (2-ethylhexyl) esters.

As examples of amines with which the phosphoric acid esters are blocked, especially tertiary amines, such as bicyclic amines, such as. As diazabicyclootan (DABCO), diazabicyclononene (DBN), diazabicycloundecene (DBU), dimethyldodecylamine or triethylamine to call. Particularly preferred for blocking the phosphoric acid esters tertiary amines are used, which ensure good activity of the catalyst under the curing conditions of 140 ° C.

Certain amine-blocked phosphoric acid catalysts are also commercially available (eg, Nacure types from King Industries). By way of example, mention may be made of the Nacure 4167 from King Industries as a particularly suitable catalyst based on an amine-blocked phosphoric acid partial ester.

The catalysts are preferably used in proportions of from 0.01 to 20% by weight, particularly preferably in proportions of from 0.1 to 10% by weight, based on the nonvolatile constituents of the coating composition according to the invention. A lower efficiency of the catalyst can be partially compensated by correspondingly higher amounts.

The coating compositions according to the invention may also contain a further amine catalyst based on a bicyclic amine, in particular an unsaturated bicyclic amine. Examples of suitable amine catalysts are 1,5-diazabicyclo [4.3.0] non-5-ene or 1,8-diazabicyclo [5.4.0] undec-7-ene.

These amine catalysts are preferably used in proportions of from 0.01 to 20% by weight, more preferably in proportions of from 0.1 to 10% by weight, based on the nonvolatile constituents of the coating composition according to the invention.

Suitable solvents for the coating compositions of the invention are, in particular, those which are chemically inert in the coating composition compared to the compounds (A), (B) and, if appropriate, (C) and which also do not react with (A) and (B) during the curing of the coating composition. react. Examples of such solvents are aliphatic and / or aromatic hydrocarbons such as toluene, xylene, solvent naphtha, Solvesso 100 or hydrosol ^® (Fa. Aral), ketones such as acetone, methyl ethyl ketone or methyl amyl ketone, esters such as ethyl acetate, butyl acetate, pentyl acetate or ethyl ethoxypropionate, ether or mixtures of the abovementioned solvents. The aprotic solvents or solvent mixtures preferably have a water content of not more than 1% by weight, more preferably not more than 0.5% by weight, based on the solvent.

In addition to the compounds (A), (B) and, if appropriate, (C) it is also possible to use further binders (E) which are preferably bonded to the hydroxyl groups of the poly (meth) acrylate (A) and / or to the free isocyanate groups of the compound ( B) and / or with the alkoxysilyl groups of the compounds (B) and / or (C) and can form network points.

For example, aminoplast resins and / or epoxy resins can be used as component (E). Suitable are the customary and known amino resins whose methylol and / or methoxymethyl groups may be partially defunctionalized by means of carbamate or allophanate groups. Crosslinking agents of this type are described in the patents US-A-4,710,542 and EP-B-0 245 700 as well as in the article of B. Singh and coworkers "Carbamylmethylated Melamines, Novel Crosslinkers for the Coatings Industry" in Advanced Organic Coatings Science and Technology Series, 1991, Volume 13, pages 193 to 207 , described.

In general, such components (E) are used in proportions of up to 40% by weight, preferably of up to 30% by weight, particularly preferably of up to 25% by weight, based on the nonvolatile constituents of the coating composition ,

In addition, the binder mixture according to the invention or the coating composition according to the invention may contain at least one customary and known coating additive (F) in effective amounts, ie. H. in amounts preferably up to 30 wt .-%, particularly preferably up to 25 wt .-% and in particular up to 20 wt .-%, each based on the nonvolatile constituents of the coating composition.

• – insbesondere UV-Absorber;
• – insbesondere Lichtschutzmittel wie HALS-Verbindungen, Benztriazole oder Oxalanilide;
• – Radikalfänger;
• – Slipadditive;
• – Polymerisationsinhibitoren;
• – Entschäumer;
• – Reaktivverdünner, wie sie aus dem Stand der Technik allgemein bekannt sind, welche bevorzugt inert gegenüber den -Si(OR)3-Gruppen sind.
• – Netzmittel wie Siloxane, fluorhaltige Verbindungen, Carbonsäurehalbester, Phosphorsäureester, Polyacrylsäuren und deren Copolymere oder Polyurethane;
• – Haftvermittler wie Tricyclodecandimethanol;
• – Verlaufmittel;
• – filmbildende Hilfsmittel wie Cellulose-Derivate;
• – Füllstoffe wie beispielsweise Nanopartikel auf der Basis von Siliziumdioxid, Aluminiumoxid oder Zirkoniumoxid; ergänzend wird noch auf das Römpp Lexikon >>Lacke und Druckfarben<< Georg Thieme Verlag, Stuttgart, 1998, Seiten 250 bis 252 , verwiesen;
• – rheologiesteuernde Additive, wie die aus den Patentschriften WO 94/22968 , EP-A-0 276 501 , EP-A-0 249 201 oder WO 97/12945 bekannten Additive; vernetzte polymere Mikroteilchen, wie sie beispielsweise in der EP-A-0 008 127 offenbart sind; anorganische Schichtsilikate wie Aluminium-Magnesium-Silikate, Natrium-Magnesium- und Natrium-Magnesium-Fluor-Lithium-Schichtsilikate des Montmorillonit-Typs; Kieselsäuren wie Aerosile^®; oder synthetische Polymere mit ionischen und/oder assoziativ wirkenden Gruppen wie Polyvinylalkohol, Poly(meth)acrylamid, Poly(meth)acrylsäure, Polyvinylpyrrolidon, Styrol-Maleinsäureanhydrid- oder Ethylen-Maleinsäure-anhydrid-Copolymere und ihre Derivate oder hydrophob modifizierte ethoxylierte Urethane oder Polyacrylate;
• – Flammschutzmittel und/oder
• – Wasserfänger.

Examples of suitable paint additives (F) are:

• - in particular UV absorber;
• In particular light stabilizers, such as HALS compounds, benzotriazoles or oxalanilides;
• - radical scavengers;
• - panty additives;
• - polymerization inhibitors;
• Defoamer;
• Reactive diluents, as are well known in the art, which are preferably inert to the -Si (OR) 3 groups.
• Wetting agents such as siloxanes, fluorine-containing compounds, carboxylic acid monoesters, phosphoric esters, polyacrylic acids and their copolymers or polyurethanes;
• - adhesion promoters such as tricyclodecanedimethanol;
• - leveling agent;
• - film-forming aids such as cellulose derivatives;
• - Fillers such as nanoparticles based on silica, alumina or zirconia; in addition, it is still on the Römpp lexicon >> Paints and Printing Inks << Georg Thieme Verlag, Stuttgart, 1998, pages 250 to 252 , directed;
• Rheology control additives, such as those from the patents WO 94/22968 . EP-A-0 276 501 . EP-A-0 249 201 or WO 97/12945 known additives; crosslinked polymeric microparticles, as described for example in the EP-A-0 008 127 are disclosed; inorganic phyllosilicates such as aluminum-magnesium silicates, sodium magnesium and sodium magnesium fluorine lithium phyllosilicates of the montmorillonite type; Silicas such as Aerosils ^®; or synthetic polymers having ionic and / or associative groups such as polyvinyl alcohol, poly (meth) acrylamide, poly (meth) acrylic acid, polyvinylpyrrolidone, styrene Maleic anhydride or ethylene-maleic anhydride copolymers and their derivatives or hydrophobically modified ethoxylated urethanes or polyacrylates;
• Flame retardants and / or
• - water catcher.

In a further embodiment of the invention, the binder mixture according to the invention or the coating composition of the invention may contain further pigments and / or fillers and serve to produce pigmented topcoats. The pigments and / or fillers used for this purpose are known to the person skilled in the art.

Since the coatings according to the invention prepared from the coating compositions according to the invention also adhere well to already cured electrodeposition coatings, surfacer finishes, basecoats or customary and known clearcoats, they are excellently suitable for automotive refinish and / or for the coating of automotive paint in addition to use in automotive OEM (OEM) Automotive attachments or the modular scratch resistant equipment of already painted automobile bodies.

The application of the coating composition according to the invention can by all the usual application methods, such as. As spraying, knife coating, brushing, pouring, dipping, watering, trickling or rolling done. In this case, the substrate to be coated can rest as such, with the application device or system being moved. However, the substrate to be coated, in particular a coil, can also be moved, with the application system resting relative to the substrate or being moved in a suitable manner.

Preferably, spray application methods are used, such as compressed air spraying, airless spraying, high rotation, electrostatic spray application (ESTA), optionally combined with hot spray application such as hot air hot spraying.

The curing of the applied coating compositions according to the invention can take place after a certain rest period. The rest period serves, for example, for the course and degassing of the paint layers or for the evaporation of volatile components such as solvents. The rest period can be supported and / or shortened by the application of elevated temperatures and / or by a reduced air humidity, provided that no damage or changes in the paint layers occur, such as premature complete crosslinking.

The thermal curing of the coating compositions has no special features, but is carried out by the usual and known methods such as heating in a convection oven or irradiation with IR lamps. Here, the thermal curing can also be done gradually. Another preferred curing method is near infrared (NIR) curing.

Advantageously, the thermal curing is carried out at a temperature of 30 to 200 ° C, more preferably 40 to 190 ° C and in particular 50 to 180 ° C for a time of 1 min to 10 h, more preferably 2 min to 5 h and in particular 3 min to 3 h, wherein for the automotive refinishing and for the coating of plastic parts applied temperatures, which are preferably between 30 and 90 ° C, longer curing times can be used.

The coating compositions of the invention have a high solids content and provide new cured coatings, especially coatings, especially clearcoats, moldings, especially optical moldings, and cantilevered films that are highly scratch resistant, the high scratch resistance remains even after a long-term exposure. At the same time, the coatings obtained according to the invention also have a very good overall appearance. Finally, the coatings and coatings according to the invention, especially the clearcoats, can also be produced in layer thicknesses> 40 μm without stress cracks occurring.

The coating compositions according to the invention are therefore outstandingly suitable as decorative, protective and / or effective, highly scratch-resistant coatings and finishes of bodies of vehicles (especially motor vehicles, such as motorcycles, buses, trucks or cars) or parts thereof; of buildings in the interior and exterior; of furniture, windows and doors; of plastic moldings, in particular CDs and windows; of industrial small parts, of coils, containers and packaging; of white goods; of films; of optical, electrotechnical and mechanical components as well as glass hollow bodies and everyday objects.

In particular, the coating compositions and finishes of the invention, in particular the clearcoats, in the technologically and aesthetically particularly demanding field of automotive OEM (OEM) and for coating plastic attachments for car bodies, especially for bodies of cars of the upper class, such. As for the production of roofs, tailgates, hoods, fenders, bumpers, spoilers, sills, protective strips, side panels u. Ä., As well as the automotive refinishing used.

The plastic parts usually consist of ASA, polycarbonates, blends of ASA and polycarbonates, polypropylene, polymethylmethacrylates or impact-modified polymethylmethacrylates, in particular of blends of ASA and polycarbonates, preferably with a polycarbonate content> 40%, in particular> 50%.

ASA is generally understood to mean impact-modified styrene / acrylonitrile polymers in which graft copolymers of vinylaromatic compounds, in particular styrene, and of vinyl cyanides, in particular acrylonitrile, are present on polyalkyl acrylate rubbers in a copolymer matrix of, in particular, styrene and acrylonitrile.

The coating compositions of the invention are particularly preferably used in multistage coating processes, in particular in processes in which a pigmented basecoat film is applied to an optionally precoated substrate, followed by a coating with the coating composition of the invention. The invention therefore also relates to effect and / or coloring multicoat paint systems comprising at least one pigmented basecoat film and at least one clearcoat film disposed thereon, which are characterized in that the clearcoat film has been prepared from the coating composition according to the invention.

Both waterborne basecoats and basecoats based on organic solvents can be used. Suitable basecoats are for example in the EP-A-0 692 007 and in those in column 3, lines 50ff. described documents. Preferably, the applied basecoat is first dried, that is, the basecoat film is removed in an evaporation phase, at least a portion of the organic solvent or of the water. The drying is preferably carried out at temperatures from room temperature to 80 ° C. After drying, the coating composition according to the invention is applied. Subsequently, the two-coat coating is preferably under conditions used in automotive OEM finishing at temperatures of 30 to 200 ° C, more preferably 40 to 190 ° C and especially 50 to 180 ° C, for a time of 1 min to 10 h, more preferably 2 min up to 5 hours and especially 3 minutes to 3 hours, wherein longer curing times may also be used for the automotive refinish temperatures, which are preferably between 30 and 90 ° C.

In a further preferred embodiment of the invention, the coating composition of the invention is used as a transparent clearcoat for coating plastic substrates, in particular plastic attachment parts. The plastic add-on parts are preferably likewise coated in a multi-stage coating process in which a pigmented basecoat film and then a first or subsequent substrate (for example flaming, corona or plasma treatment of the substrate) may be precoated or pretreated for better adhesion of the subsequent coatings Layer can be applied with the coating compositions of the invention.

Finally, the coating composition according to the invention is used as a transparent clearcoat for the coating of transparent plastic substrates. In this case, the coating compositions include UV absorbers, which are designed in quantity and type also on the effective UV protection of the plastic substrate.

Examples

Preparation of a poly (meth) acrylate resin with hydroxyl groups (A1)

In a, by means of oil circulation thermostat heatable, double-walled 4-l stainless steel vessel, equipped with thermometer, anchor stirrer, 2 dropping funnels and reflux condenser solvent is submitted to the polymerization. In one of the dropping funnel, the monomer mixture, in the second dropping funnel, the Intiatorlösung containing a suitable initiator (usually a peroxide), submitted. The original is heated to a polymerization temperature of 140 ° C. After reaching the polymerization temperature, the initiator feed is started first. 15 minutes after the start of the initiator feed, the monomer feed (duration 240 Minutes). The initiator feed is adjusted so that it continues to run for another 30 minutes after the end of the monomer feed. After completion of the Initiatorzulaufes the mixture is stirred for a further 2 h at 140 ° C and then cooled to room temperature. The reaction mixture is then adjusted to the solids content indicated in 2 using solvent. Table 1: Composition of the polymethacrylate (A1) in parts by weight component Parts by weight styrene 8.0 n-butyl methacrylate 8.0 acrylic acid 0.6 4-hydroxybutyl acrylate 12.0 2-hydroxyethyl acrylate 12.0 n-butyl acrylate 19.0 Table 2: Characteristics of the polymethacrylate (A1) (acid number and viscosity determined experimentally, OH number and Tg calculated theoretically) Solid 1 h 150 ° C 65% Säurez. (measured) [mg KOH / g] 8-12 OH number calculated [mg KOH / g] 175 Tg (FOX) [° C] -27 Viscosity [mPa.s] ¹⁾ 2200 ¹⁾ Determined at room temperature DIN53229 with a cone-plate viscometer from Brookfield, cone 3

Preparation of a Low-Viscosity, Caprolactone-Modified Poly (meth) Acrylate Resin Having Hydroxyl Groups (A2)

290 g of butyl acetate and 290 g Solventnaphta are placed in a stainless steel stirred tank with anchor stirrer and reflux condenser and heated to 167 ° C. with stirring under nitrogen at a pressure of 3.5 bar in a nitrogen atmosphere. A solution of 288.8 g of di-tert-amyl peroxide and 10.7 g of butyl acetate and 10.8 g Solventnaphta is added dropwise over 275 min. The monomer mixture of 400 g of styrene, 550 g of butyl methacrylate, 803.3 g of hydroxyethyl acrylate, 550 g of ethylhexyl acrylate and 102.9 g of acrylic acid is added dropwise uniformly over 240 minutes. The monomer feed is started 5 minutes after the initiator feed. After completion of the feeds, the reactor contents are kept for a further 20 minutes at 167 ° C and then added 993 g of caprolactone within one hour, while the reactor temperature is lowered evenly to 150 ° C. After completion of the feed is stirred at 150 ° C for a further 1.5 h. Subsequently, the reactor contents are cooled, at a temperature below 121 ° C, the pressure is released and emptied at 80 ° C, the reactor. The resulting polymer solution has a solids content of 81.2% at a viscosity of 2400 mPa · s. The binder has a weight average molecular weight of 5300 g / mol with a uniformity of 3.0 (determined with GPC versus polystyrene calibration). Table 3: Composition of polymethacrylate (A2) in parts by weight component Parts by weight styrene 16.6 n-butyl methacrylate 22.9 acrylic acid 4.3 ethylhexyl acrylate 22.9 2-hydroxyethyl acrylate 33.4 Table 4: Ratios of the polymethacrylate (A2) (acid number determined experimentally, OH number determined experimentally) A2 Solids [%] (1 h 130 ° C) 81.2 Acid number [mg KOH / g] 27.6 OH number [mg KOH / g] 122 Viscosity [mPa.s] ¹⁾ 2400 ¹⁾ Determined at room temperature DIN53229 with a cone-plate viscometer from Brookfield, cone 3

Preparation of a hardener (B1) according to the invention based on a dimeric, HDI-based uretdione (10 mol% monosilane structures IIa and 90 mol% bis-silane structures IIIa: degree of conversion of the isocyanate groups c = 40 mol%)

A steel reactor equipped with a reflux condenser and a thermometer is charged with 48.3 parts of dimerized hexamethylene diisocyanate (HDI) containing uretdione groups (Bayer Desmodur N3400), 12.1 parts of butyl acetate and 2.4 parts of triethyl orthoformate. About a dropping funnel then a mixture of 30.7 parts of bis [3- (trimethoxysilyl) propyl] amine (Dynasylan 1124, EVONIK, Rheinfelden) and 2.4 parts of trimethoxysilylpropyl-N-butylamine (Dynasilan 1189, EVONIK, Rheinfelden) under Nitrogen veiling and stirring are added dropwise. It is a slight increase in temperature to about 40 ° C to observe. After 2 hours of stirring, the NCO value is checked titrimetrically: NCO content: 6.6% (solution). The nonvolatile fraction (1 h, 150 ° C) is 85%.

Preparation of a noninventive hardener (BV1) based on closely distributed HDI-based isocyanurate (10 mol% monosilane structures IIa and 90 mol% bis-silane structures IIIa: degree of conversion of the isocyanate groups c = 40 mol%)

A steel reactor equipped with a reflux condenser and a thermometer is charged with 57.6 parts of trimerized hexamethylene diisocyanate (HDI) (Desmodur N3600 Bayer), 14.8 parts of butyl acetate and 2.8 parts of triethyl orthoformate. About a dropping funnel is then a mixture of 39.4 parts of bis [3- (trimethoxysilyl) propyl] amine (Dynasylan 1124, EVONIK, Rheinfelden) and 3.0 parts of trimethoxysilylpropyl-N-butylamine (Dynasilan 1189, EVONIK, Rheinfelden) under Nitrogen veiling and stirring are added dropwise. It is a slight increase in temperature to about 40 ° C to observe. After stirring for 2 hours, the NCO value is checked titrimetrically: NCO content: 6.6% (solution) nonvolatile fraction (1 h, 150 ° C.): 85%,

Preparation of a non-inventive hardener (BV2) based on widely distributed HDI-based isocyanurate (10 mol% monosilane structures IIa and 90 mol% bis-silane structures IIIa: degree of conversion of the isocyanate groups c = 40 mol%)

A steel reactor equipped with a reflux condenser and a thermometer is charged with 67.6 parts of trimerized hexamethylene diisocyanate (HDI) (Desmodur N3300 from Bayer), 16.9 parts of butyl acetate and 3.4 parts of triethyl orthoformate. Via a dropping funnel is then a mixture of 43.0 parts of bis [3- (trimethoxysilyl) propyl] amine (Dynasylan 1124, EVONIK, Rheinfelden) and 3.3 parts of trimethoxysilylpropyl-N-butylamine (Dynasilan 1189, EVONIK, Rheinfelden) under Nitrogen veiling and stirring are added dropwise. It is a slight increase in temperature to about 40 ° C to observe. After 2 hours of stirring, the NCO value is checked titrimetrically: NCO content: 6.6% (solution). non-volatile content (1 h, 150 ° C): 85%

Formulation of the coating compositions B1 and B2 according to the invention and of the coatings of Examples 1 and 2 according to the invention and of the coating compositions VB1 to VB4 of Comparative Examples C1 to V4 and the coatings of Comparative Examples C1 to V4

In the order given (starting from the top), the constituents specified in Table 5 and Table 6 are intimately mixed in a suitable vessel and immediately afterwards applied to a mirror base painted with black basecoat (basecoat drying for 30 minutes at 80 ° C., 10 minutes flash off time). , Subsequently, the sheets are dried at 60 ° C for 30 minutes in the oven. The obtained Coatings are stored for 24 h at room temperature and measured with a Wave-Scan ^® BYK-Gardner. The test subjects are shown in Table 7 and Table 8. Table 5: Composition of the coating composition B1 according to the invention and the coating compositions VB1 and VB2 of the comparative examples C1 and C2, in each case based on the hydroxyl-containing polymethacrylate (A1) Example B1 Comp Ex. VB1 Comp Ex. VB2 Polyacrylate (A1) 40 40 40 Dynoadd F1 ¹⁾ 0.2 0.2 0.2 Tinuvin ^® 384 ²⁾ 0.5 0.5 0.5 Tinuvin ^® 292 ³⁾ 0.5 0.5 0.5 butyl 8th 8th 8th Nacure 4167 ^{® 4)} 1.2 1.2 1.2 Hardener B1 50 Hardener BV1 (Cf.) 50 Hardener BV2 (Cf.) 50 non-volatile content (1 h, 150 ° C) 70% 70% 70% ¹⁾ Dynoadd F1 = commercially available, multifunctional, surface-active additive from Hertfelder GmbH, Bielefeld
²⁾ Tinuvin ^® 384 = commercial light stabilizer based on a benzotriazole from Ciba
³⁾ Tinuvin ^® 292 = commercial light stabilizer based on a sterically hindered amine from Ciba
⁴⁾ Nacure ^® 4167 = commercial catalyst based on aminblockiertem Phosphorsäureteilester from King Industries, non-volatile content 25% Table 6: Composition of the coating agent B2, VB3 and VB4, (in each case based on the hydroxyl-containing polymethacrylate, caprolactone-modified A2) Example B2 Comp Ex. VB3 Comp Ex. VB4 Polyacrylate A2 41 41 41 Dynoadd F1 ¹⁾ 0.2 0.2 0.2 Tinuvin ^® 384 ²⁾ 0.5 0.5 0.5 Tinuvin ^® 292 ³⁾ 0.5 0.5 0.5 butyl 8th 8th 8th Nacure 4167 ^{® 4)} 1 1 1 Hardener B1 45 Hardener BV1 (Cf.) 45 Hardener BV2 (Cf.) 45 non-volatile content (1 h, 150 ° C) 75% 75% 75% Table 7: Test results of the coatings Basecoat sheet 1 without clearcoat Example B1 on basecoat sheet 1 Basecoat sheet 2 without clearcoat Comp Ex. VB1 on basecoat sheet 2 Basecoat sheet 3 without clearcoat Comp Ex. VB2 on basecoat sheet 3 SD (microns) 15 39 15 41 16 39 SW 8.0 1.7 8.1 10.3 7.8 85.4 LW 2.4 2.2 2.6 14.6 2.4 60.3 Table 8: Test results of the coatings of Inventive Example 2 and the coatings of Comparative Examples V3 and V4 Basecoat Sheet 4 without clearcoat Example B2 on basecoat sheet 4 Basecoat sheet 5 without clearcoat Comp Ex. VB3 on basecoat sheet 5 Basecoat sheet 6 without clearcoat Comp Ex. VB4 on basecoat sheet 6 SD (μm) 15 39 15 41 17 39 SW 8.3 1.6 8.1 9.7 8.7 18.9 LW 2.4 0.7 2.2 21.3 2.2 25.5

All coatings are dry to the touch after drying (30 minutes at 60 ° C). Possibility of occurrence of adhesive films in different optimal laboratory conditions can be easily stopped by slightly increased amounts of catalyst and / or more effective catalysts.

Summary of the test results:

The comparison of both the long-wave values (LW) and the short-wave values (SW) in Table 7 of Example 1 according to the invention with those of Comparative Example V1 and Comparative Example V2 shows that Inventive Example 1 has significantly better values than the Comparative Examples V1 and V2, d. H. the coating composition B1 according to the invention shows a significantly better course than the coating compositions of the comparative examples V1 and V2.

Analogously, the comparison of both the long-wave values (LW) and the short-wave values (SW) in Table 8 of Inventive Example 2 with those of Comparative Example V3 and Comparative Example V4 shows that Example 2 according to the invention has significantly better values has as the comparative examples V3 and V4, d. H. the coating composition B2 according to the invention shows a significantly better course than the coating compositions of the comparative examples V3 and V4.

In addition, by comparing the coating composition B1 according to the invention with the coating composition B2 according to the invention, the nonvolatile content of the coating composition can be further increased with a caprolactone-modified binder (A2) and the resulting coating of Example B2, despite the increased nonvolatile content of the coating composition B2, has a Comparing with the coating of Example 1 consistently responsive optical quality.

QUOTES INCLUDE IN THE DESCRIPTION

This list of the documents listed by the applicant has been generated automatically and is included solely for the better information of the reader. The list is not part of the German patent or utility model application. The DPMA assumes no liability for any errors or omissions.

Cited patent literature

• WO 08/74491 [0002]
• WO 08/74490 [0002]
• WO 08/74489 [0002]
• WO 08/074489 [0002]
• US 5691439 A [0004]
• EP 1273640 A [0005, 0041]
• WO 2001/98393 [0006]
• EP 1426393 A [0007, 0024]
• EP 0994117 A [0041]
• WO 01/09260 A [0041]
• US 4546046A [0050]
• WO 05/03340 [0062]
• DE 102005045228 A [0064]
• US 4710542 A [0074]
• EP 0245700 B [0074]
• WO 94/22968 [0077]
• EP 0276501 A [0077]
• EP 0249201 A [0077]
• WO 97/12945 [0077]
• EP 0008127A [0077]
• EP 0692007A [0091]

Cited non-patent literature

• DIN 53240-2 [0039]
• DIN-EN-ISO 11357-2 [0040]
• DIN-EN-ISO 11357-2 [0043]
• DIN 53240-2 [0045]
• DIN EN ISO 2114 [0045]
• B. Singh and coworkers "Carbamylmethylated Melamines, Novel Crosslinkers for the Coatings Industry" in Advanced Organic Coatings Science and Technology Series, 1991, Volume 13, pages 193 to 207 [0074]
• >> Paints and Printing Inks << Georg Thieme Verlag, Stuttgart, 1998, pages 250 to 252 [0077]
• DIN53229 [0094]
• DIN53229 [0095]

Claims (13)

Coating composition based on aprotic solvents, containing at least one oligomeric and / or polymeric hydroxyl group-containing compound (A) and at least one compound (B) with isocyanate groups and having at least one silane group of the formula (I) -X-Si-R " _x G _3-x (I) with G = identical or different hydrolyzable groups, in particular G = alkoxy group (OR '), R' = hydrogen, alkyl or cycloalkyl, where the carbon chain may be interrupted by non-adjacent oxygen, sulfur or NRa groups, with Ra = alkyl , Cycloalkyl, aryl or aralkyl, preferably R '= ethyl and / or methyl, X = organic radical, in particular linear and / or branched alkylene or cycloalkylene radical having 1 to 20 carbon atoms, very particularly preferably X = alkylene radical having 1 to 4 carbon atoms, R '' = alkyl, cycloalkyl, aryl, or aralkyl, wherein the carbon chain may be interrupted by non-adjacent oxygen, sulfur or NRa groups, with Ra = alkyl, cycloalkyl, aryl or aralkyl, preferably R "= alkyl radical, in particular having 1 to 6 C atoms, x = 0 to 2, preferably 0 to 1, particularly preferably x = 0, characterized in that (i) the isocyanate-containing and silane-containing compound (B) has uretdione groups and ( ii) the compound (B) has been prepared from a linear aliphatic diisocyanate (DI). Coating composition according to Claim 1, characterized in that the compound (B) consists of a linear, aliphatic diisocyanate (DI) having 3 to 12 C atoms, in particular having 4 to 10 C atoms and very particularly preferably having 5 to 6 C atoms , has been prepared. Coating composition according to claim 1 or 2, characterized in that the compound (B) consists of a polyisocyanate (PI) having a uretdione group content of> 50 mol%, preferably more than 50 to 90 mol%, particularly preferably 65 to 80 mol%, each based on the totality of the resulting by isocyanate oligomerization of the linear aliphatic diisocyanate (DI) structural types, has been prepared. Coating composition according to one of claims 1 to 3, characterized in that the compound (B) is between 2.5 and 90 mol%, based on the totality of the structural units (II) and (III), of at least one structural unit of the formula (II) -NR- (X-SiR "x (OR ') 3-x) (II), and between 2.5 and 90 mol%, based on the entirety of the structural units (II) and (III), of at least one structural unit of the formula (III) -N (X-SiR''x (OR ') 3-x) n (X'-SiR''y (OR') 3-y) m (III) wherein R = hydrogen, alkyl, cycloalkyl, aryl or aralkyl, wherein the carbon chain may be interrupted by non-adjacent oxygen, sulfur or NRa groups, with Ra = alkyl, cycloalkyl, aryl or aralkyl, R '= hydrogen, Alkyl or cycloalkyl, wherein the carbon chain may be interrupted by non-adjacent oxygen, sulfur or NRa groups, with Ra = alkyl, cycloalkyl, aryl or aralkyl, preferably R '= ethyl and / or methyl X, X' = linear and or branched alkylene or cycloalkylene radical having 1 to 20 carbon atoms, preferably X, X '= alkylene radical having 1 to 4 carbon atoms, R "= alkyl, cycloalkyl, aryl, or aralkyl, wherein the carbon chain by non-adjacent oxygen, sulfur or NRa groups may be interrupted, with Ra = alkyl, cycloalkyl, aryl or aralkyl, preferably R "= alkyl radical, in particular having 1 to 6 C atoms, n = 0 to 2, m = 0 to 2, m + n = 2, and x, y = 0 to 2. Coating composition according to one of Claims 1 to 4, characterized in that the total proportion of the isocyanate groups in the polyisocyanate (PI) reacted with the structural units (II) and / or (III) is between 5 and 95 mol%, preferably between 10 and 85 mol%. %, and more preferably between 15 and 70 mol%. Coating composition according to one of claims 1 to 5, characterized in that compound (B) is the reaction product of the uretdione of 1,6-hexamethylene diisocyanate with bis (3-propyltrimethoxysilyl) amine and N- (3- (trimethoxysilyl) propyl) butylamine , Coating composition according to one of claims 1 to 6, characterized in that the hydroxyl-containing compound (A) is selected from the group of polyacrylate polyols, polymethacrylate polyols, polyester polyols, polyurethane polyols and / or polysiloxane, in particular from the group of polyacrylate polyols and / or the polymethacrylate polyols. Coating composition according to one of claims 1 to 7, characterized in that it contains as compound (A) lactone-modified, preferably ε-caprolactone-modified, hydroxyl-containing oligomeric and / or polymeric compounds (A) and very particularly preferably ε-caprolactone-modified hydroxyl-containing polyacrylate polyols and / or ε- contains caprolactone-modified hydroxyl-containing polymethacrylate polyols. Coating composition according to one of claims 1 to 9, characterized in that the coating composition contains a phosphorus-containing catalyst for the crosslinking of the silane groups. Multi-stage coating process, characterized in that a pigmented basecoat film is applied to an optionally precoated substrate and then a layer of the coating composition according to one of Claims 1 to 9 is applied. Multi-stage coating method according to claim 10, characterized in that after application of the pigmented basecoat layer of the applied basecoat is first dried at temperatures from room temperature to 80 ° C and after the application of the coating composition according to any one of claims 1 to 9 at temperatures of 30 to 90 ° C. cured for a period of 1 minute to 10 hours. Use of the coating composition according to one of claims 1 to 9 as a clearcoat for automotive refinishing and / or for the coating of automotive components and / or plastic substrates. Application of the method according to claim 10 or 11 for the automotive refinishing and / or for the coating of plastic substrates.