EP1368396A1

EP1368396A1 - Aqueous primary dispersion, substantially or completely devoid of volatile organic substances, method for the production thereof and use of the same

Info

Publication number: EP1368396A1
Application number: EP02701273A
Authority: EP
Inventors: Ralf Nickolaus; Heinz-Peter Rink; Reinhold Clauss; Elisabeth Wessling; Wilma LÖCKEN; Nicole Freitag; Dunja Mikolajetz
Original assignee: BASF Coatings GmbH
Current assignee: BASF Coatings GmbH
Priority date: 2001-02-13
Filing date: 2002-02-13
Publication date: 2003-12-10
Also published as: US20040048968A1; DE10106567A1; WO2002064652A1; US7157526B2

Abstract

The invention relates to an aqueous primary dispersion, substantially or completely devoid of volatile organic substances, containing dispersed and/or emulsified solid and/or liquid polymer particles and/or dispersed solid core-shell particles with a particle diameter </= 500 nm. Said dispersion is obtained by the radical micro- or mini-emulsion polymerisation of at least one olefinically unsaturated monomer, in the presence of at least one hydrophobic additive and at least one oligomeric polyester with a number average molecular weight of between 150 and 1,500 dalton, a hydroxyl value of between 100 and 1,000 mg KOH/g and an acid value < 20 mg KOH/g. The invention also relates to a method for the production of said dispersion and to the use thereof as a coating substance, adhesive and sealant or for producing a coating substance, adhesive or sealant.

Description

Aqueous primary dispersion essentially or completely free of volatile organic substances, process for their preparation and their use

The present invention relates to new aqueous primary dispersions which contain dispersed and / or emulsified, solid and / or liquid polymer particles and / or dispersed solid core-shell particles of a particle diameter <500 nm. The present invention also relates to a new process for the preparation of the new aqueous primary dispersions by free-radical micro- and mini-emulsion polymerization. Furthermore, the present invention relates to the use of the new aqueous primary dispersions as broom sealants, adhesives and sealants or for the production of coating materials, adhesives and sealants, in particular coating materials for the production of single- or multi-layer clearcoats and single- or multi-layer color and / or effect coatings for the automotive painting, the painting of buildings inside and outside, the painting of doors, windows and furniture, the industrial painting, including coil coating, container coating and the impregnation and / or coating of electrical components, as well as the painting of white goods, including household appliances, boilers and radiators.

Micro and mini emulsions are dispersions of water, an oil phase and one or more surface-active substances which have droplet sizes from 5 to 50 nm (microemulsions) or from 50 to 500 nm. Microemulsions are considered to be thermodynamically stable, whereas the mini emulsions are considered to be metastable (cf. Emulsion Polymerization and Emulsion Polymers, editors. PA Lovell and Mohamed S. El-Aasser, John Wiley and Sons, Chichester, New York, Weinheim, 1997, pages 700 and following; Mohamed S. El-Aasser, Advances in Emulsion Polymerization and Latex Technology, 30 ^th Annual Short Course, Volume 3, June 7-11, 1999, Emulsion Polymers Institute, Lehigh University, Bethlehem, Pennsylvania, USA). Both types of dispersions are widely used in technology, for example in cleaners, cosmetics or personal care products. However, instead of the usual macroemulsions in which droplet sizes> 1,000 nm are present, they can also be used for polymerization reactions.

The production of aqueous primary dispersions with the aid of radical mini-emulsion polymerization is, for example, from the international

Patent application WO 98/02466 or the German patent DE

196 28 143 A 1 and DE 196 28 142 A 1 known. With these known

Processes, the monomers can be copolymerized in the presence of different low molecular weight, oligomeric or polymeric hydrophobic substances, which are also referred to as costabilizers.

In addition, hydrophobic, water-insoluble organic

Aids such as plasticizers, improvers of the stickiness of the resulting film, film-forming aids or other unspecified organic additives are incorporated into the monomer droplets of the mini emulsion. The use of the known aqueous primary dispersions for the production of

Coating materials are not apparent from the patents.

Aqueous coating materials based on aqueous primary dispersions which contain solid core-shell particles and have been prepared by mini-emulsion polymerization of monomers in the presence of hydrophobic polymers are known from the patents EP-A-0 401 565, WO 97/49739 or EP -A-0 755 946. The use of oligomeric polyesters with comparatively high hydroxyl numbers is not apparent from these patents. As Clearcoats, however, provide the known aqueous coating materials, clearcoats which tend to form haze.

The non-prepublished German patent application DE 199 59 928.9 from BASF Coatings AG with the internal file number PAT 99 174 DE and the title "Aqueous primary dispersions and coating materials, process for their preparation and their use" describes aqueous primary dispersions and coating materials which disperse and / or contain emulsified, solid and / or liquid polymer particles and / or dispersed solid core-shell particles of a particle diameter <500 nm and by radical micro- or miniemulsion polymerization of at least one olefinically unsaturated monomer in the presence of at least one hydrophobic crosslinking agent for the from the Monomer or the (co) polymer resulting from the monomers can be prepared.

The non-prepublished German patent application DE 199 59 927.0 from BASF Coatings AG with the internal file number PAT 99 173 DE and the title "Aqueous primary dispersions and coating materials, process for their preparation and their use" describes aqueous primary dispersions and coating materials which disperse and / or contain emulsified, solid and / or liquid polymer particles and / or dispersed solid core-shell particles with a particle diameter <500 nm and can be prepared by radical micro- or miniemulsion polymerization of an olefinically unsaturated monomer and a diarylethylene.

In the unpublished German patent application DE 199 24

674.2 from BASF Coatings AG with the internal file number PAT 99 198 DE and the title “Aqueous primary dispersions and coating materials,

Processes for their preparation and their use "become aqueous Primary dispersions and coating materials described which contain dispersed and / or emulsified, solid and / or liquid polymer particles and / or dispersed solid core-shell particles with a particle diameter <500 nm and by radical micro- or miniemulsion polymerization of an olefinically unsaturated monomer and a diarylethylene in the presence of at least one hydrophobic crosslinking agent for the copolymer resulting from the monomers can be prepared.

In the unpublished German patent application DE 100 05 814.1 from BASF Coatings AG with the internal file number PAT 00 253 DE and the title "Aqueous primary dispersions, process for their preparation and their use" describes aqueous primary dispersions and coating materials which dispersed and / or emulsified contain solid and / or liquid polymer particles and / or dispersed solid core-shell particles with a particle diameter <500 nm and by radical micro- or miniemulsion polymerisation of at least one olefinically unsaturated monomer in the presence of at least one polyhydroxy-functionalized cyclic and / or acyclic alkane with 9 up to 16 carbon atoms can be produced in the molecule.

The unpublished German patent application DE 100 18 601.7 from BASF Coatings AG with the internal file number PAT 00 256 DE and the title "Aqueous primary dispersions and coating materials, process for their preparation and their use" describes aqueous primary dispersions and coating materials which disperse and / or contain emulsified, solid and / or liquid polymer particles and / or dispersed solid core-shell particles of a particle diameter <500 nm and by radical micro- or miniemulsion polymerization of at least one olefinic unsaturated monomer in the presence of at least one hydrophobic crosslinking agent for the (co) polymer resulting from the monomer or the monomers, the monomer or the monomers being dispersed in an aqueous dispersion of the crosslinking agent or the crosslinking agents before the (co) polymerization.

The use of oligomeric polyesters which have comparatively high hydroxyl numbers is not described in the unpublished patent applications.

It is an object of the present invention to provide a new aqueous primary dispersion which is essentially or completely free of volatile organic substances, comprising dispersed and / or emulsified, solid and / or liquid polymer particles and / or dispersed solid core-shell particles having a particle diameter of <500 nm , which can be prepared by free-radical micro- or miniemulsion polymerization of at least one olefinically unsaturated monomer in the presence of at least one hydrophobic additive. The new aqueous primary dispersion is said to exist as such as a new aqueous coating material or adhesive which is essentially or completely free of volatile organic substances or as an aqueous sealant which is substantially or completely free of volatile organic substances or for the production of a new, volatile organic substances in the suitable or completely free aqueous coating material or adhesive or a sealing compound substantially or completely free of volatile organic substances. The new aqueous primary dispersion and the new aqueous coating material or adhesive or the new aqueous sealant should be stable in storage. The new coating material is said to be particularly suitable for the production of single and multi-layer clear coatings that no longer cause turbidity (Haze) and a particularly smooth surface has a particularly good overall appearance (appearance).

Accordingly, the new aqueous primary dispersion which is essentially or completely free of volatile organic substances has been found, comprising dispersed and / or emulsified, solid and / or liquid polymer particles and / or dispersed solid core-shell particles of a particle diameter <500 nm, which can be prepared by free radicals Micro- or miniemulsion polymerization of at least one olefinically unsaturated monomer in the presence of at least one hydrophobic additive and at least one oligomeric polyester with a number average molecular weight of 150 to 1,500 daltons, a hydroxyl number of 100 to 1,000 mg KOH / g and an acid number <20 mg KOH / g.

In the following, the new aqueous primary dispersion which is essentially or completely free of volatile organic substances is referred to as "primary dispersion according to the invention".

In addition, the new process for the preparation of an aqueous primary dispersion which is essentially or completely free of volatile organic substances has been found, in which at least one olefinically unsaturated monomer is present in the presence of at least one hydrophobic additive and at least one oligomeric polyester having a number average molecular weight of 150 to 1,500 Daltons , a hydroxyl number of 100 to 1,000 mg KOH / g and an acid number <20 mg KOH / g polymerized by radical micro- or miniemulsion polymerization (co). In the following, the new process for the production of an aqueous primary dispersion which is essentially or completely free of volatile organic substances is referred to as the "process according to the invention".

Further objects according to the invention are evident from the description below.

The primary dispersions according to the invention contain dispersed and / or emulsified solid and / or liquid polymer particles and / or dispersed solid core-shell particles. The size of the polymer particles or the dispersed core-shell particles results directly from the process according to the invention described below. Here, the average particle diameter is less than 500 nm. It is preferably 10 to 500 nm, preferably 50 to 400 nm and very particularly preferably 100 to 350 nm.

The primary dispersions according to the invention have an advantageously high solids content, for example of more than 20% by weight, preferably more than 30% by weight. Solids contents of over 40% by weight can even be achieved. The primary dispersions according to the invention have a low viscosity even with a high solids content, which represents a further particular advantage of the primary dispersions according to the invention and the coating materials, adhesives or sealants according to the invention produced therefrom.

The core-shell particles result from the graft copolymerization of organic solids and the monomers described below. The organic solids are preferably hydrophobic polymers, as described, for example, in the patents EP 0 401 565 A1, page 3, lines 5 to page 4, line 50, WO 97/49739, page 4, lines 19 to Page 5, line 3, or EP 0 755 946 A1, page 3, line 26, to page 5, line 38. These hydrophobic polymers can also be made by mini-emulsion polymerization.

The primary dispersions according to the invention can also have a bimodal particle size distribution in which 0.1 to 80% by weight, in particular 1.0 to 50% by weight, of the (co) polymers resulting from the monomers has a particle size, determined using an analytical ultracentrifuge , from 20 to 500 nm, in particular 50 to 300 nm, and 20 to 99.9% by weight, in particular 50 to 99% by weight of the copolymer, have a particle size of 200 to 1,500 nm, in particular 300 to 900 nm , the particle sizes differing by at least 50 nm, in particular by at least 100 nm, very particularly preferably by at least 200 nm. With regard to the measurement method, reference is also made to lines 5 to 9 of page 6 of German patent application DE 196 28 142 A1.

The starting compound for the preparation of the primary dispersions according to the invention and for the process according to the invention is at least one olefinically unsaturated monomer.

At least two, in particular at least three, different monomers are preferably copolymerized with one another.

The monomers are particularly preferably copolymerized by the controlled free-radical micro- or mini-emulsion polymerizations, in particular mini-emulsion polymerizations. For this purpose, at least one of the monomers from the group consisting of the monomers of the general formula I R ¹ R ² C = CR ³ R ⁴ (I),

selected.

In the general formula I, the radicals R ¹ , R ² , R ³ and R ⁴ each independently represent 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 R ¹ , R ² , R ³ and R ⁴ stand for substituted or unsubstituted aryl, arylalkyl or arylcycloalkyl radicals, in particular substituted or unsubstituted aryl radicals.

Examples of suitable alkyl radicals are methyl, ethyl, propyl, isopropyl, n-butyl, isobutyl, tert-butyl, amyl, hexyl or 2-ethylhexyl.

Examples of suitable cycloalkyl radicals are cyclobutyl, cyclopentyl or cyclohexyl.

Examples of suitable alkylcycloalkyl radicals are methylenecyclohexane, ethylenecyclohexane or propane-1,3-diylcyclohexane.

Examples of suitable cycloalkylalkyl radicals are 2-, 3- or 4-methyl-, ethyl-, propyl- or butylcyclohex-1-yl.

Examples of suitable aryl radicals are phenyl, naphthyl or biphenylyl, preferably phenyl and naphthyl and in particular phenyl.

Examples of suitable alkylaryl radicals are benzyl or ethylene or propane-1,3-diyl-benzene. Examples of suitable cycloalkylaryl radicals are 2-, 3-, or 4-phenylcyclohex-1-yl.

Examples of suitable arylalkyl radicals are 2-, 3- or 4-methyl, ethyl, propyl or butylphen-1 -yl.

Examples of suitable arylcycloalkyl radicals are 2-, 3- or 4-cyclohexylphen-1-yl.

The radicals R ¹ , R ² , R ³ and R ⁴ described above can be substituted. For this purpose, electron-withdrawing or electron-donating atoms or organic residues can be used.

Examples of suitable substitutes are halogen atoms, in particular chlorine and fluorine, nitrile groups, nitro groups, partially or completely halogenated, in particular chlorinated and / or fluorinated, alkyl, cycloalkyl, alkylcycloalkyl, cycloalkylalkyl, aryl, alkylaryl, cycloalkylaryl, arylalkyl and Arylcycloalkyl radicals, including those exemplified above, in particular tert-butyl; Aryloxy, alkyloxy and cycloalkyloxy radicals, in particular phenoxy, naphthoxy, methoxy, ethoxy, propoxy, butyloxy or cyclohexyloxy; Arylthio, alkylthio and cycloalkylthio radicals, in particular phenylthio, naphthylthio, methylthio, ethylthio, propylthio, butylthio or cyclohexylthio; hydroxyl groups; and / or primary, secondary and / or tertiary amino groups, in particular amino, N-methylamino, N-ethylamino, N-propylamino, N-phenylamino, N-cyclohexylamino, N, N-dimethylamino, N, N-diethylamino, N, N -Dipropylamino, N, N-diphenylamino, N, N-dicyclohexylamino, N-cyclohexyl-N-methylamino or N-ethyl-N-methylamino.

Examples of monomers I used with particular preference are diphenylethylene, dinaphthaleneethylene, eis or trans-stilbene, vinylidene bis (4-N, N-dimethylaminobenzene), vinylidene bis (4-aminobenzene) or vinylidene bis (4-nitrobenzene).

The monomers I described above can be used individually or as a mixture of at least two monomers I.

If used, the proportion of the monomers I described above in the monomer mixture, based in each case on the monomer mixture, is preferably from 0.01 to 10, preferably from 0.1 to 9.0, particularly preferably from 0.15 to 8.0, very particularly preferably 0.2 to 7.0 and in particular 0.25 to 6.0% by weight.

With regard to the conduct of the reaction and the properties of the resulting copolymers, in particular the acrylate copolymers, diphenylethylene is of very particular advantage and is therefore used with very particular preference.

For the process according to the invention, the use of at least one monomer I has the additional significant advantage that the primary dispersions according to the invention can be prepared in a batch mode without the reaction mixture overheating or even running through the reactor.

Furthermore, it is advantageous if at least one of the monomers, which are different from the monomers I, contains reactive functional groups (a) which can undergo thermally initiated crosslinking reactions with groups of their own type or with complementary reactive functional groups (b). These reactive functional groups (a) or (b) or (a) and (b) can be present in the (co) polymers, which consist of the monomers described below or of the monomers described below and the above described monomers I result and accordingly have self-crosslinking properties. Accordingly, the relevant primary dispersions according to the invention and the coating materials, adhesives and sealants according to the invention produced therefrom are self-crosslinking.

However, the complementary reactive functional groups (a) or (b) can also be present in the crosslinking agents described below, which are added to the primary dispersions according to the invention before, during and / or after, in particular before, their preparation. The relevant primary dispersions according to the invention and the coating materials, adhesives and sealants according to the invention produced therefrom are thus cross-linking.

For the terms "self-crosslinking" and "externally crosslinking", reference is also made in addition to Römpp Lexikon Lacke und Druckfarben, Georg Thieme Verlag, Stuttgart, New York, 1998, "Härtung", pages 274 to 276.

Examples of suitable complementary reactive functional groups (a) and (b) are compiled in the following overview. In the overview, the variable R stands for an acyclic or cyclic aliphatic, an aromatic and / or an aromatic-aliphatic (araliphatic) radical; the variables R and R stand for the same or different aliphatic radicals or are linked to one another to form an aliphatic or heteroaliphatic ring.

Overview: Examples of complementary functional groups (a) and (b) (a) monomer and (b) crosslinking agent or (a) crosslinking agent and (b) monomer

-SH -C (0) -OH

-NH ₂ -C (0) -0-C (0) -

-OH -NCO

-0- (CO) -NH- (CO) -NH ₂ -NH-C (0) -OR

-0- (CO) -NH ₂ -CH ₂ -OH

> NH -CH ₂ -0-R

-NH-CH ₂ -OH

-NH-CH ₂ -OR

-N (-CH ₂ -0-R) ₂

-NH-C (0) -CH (-C (0) OR) ₂

-NH-C (0) -CH (-C (0) OR) (- C (0) -R)

-NH-C (0) -NR ^' R ^"

> Si (OR) ₂ O

/ \

-CH-CH ₂

-C (0) -OH O / \

-CH-CH ₂

The selection of the respective complementary groups (a) or (b) or (a) and (b) depends on the one hand on the fact that they do not undergo any undesirable reactions during storage of the primary dispersions according to the invention and / or if necessary do not interfere with additional curing with actinic radiation or inhibit, and on the other hand in which temperature range the crosslinking should take place.

Crosslinking temperatures of from room temperature to 180 ° C. are preferably used in the primary dispersions according to the invention or in the coating materials, adhesives and sealants produced therefrom. There are therefore preferably monomers with thio, hydroxyl, methylol, methylol ether, N-methylol, N-alkoxymethylamino, imino, carbamate, allophanate and / or carboxyl groups, but especially amino, alkoxymethylamino or hydroxyl groups, especially Hydroxyl groups, on the one hand, and crosslinking agents with anhydride, carboxy, epoxy, blocked isocyanate, urethane, methylol, methylol ether, N-methylol, N-alkoxymethylamino, siloxane, amino, hydroxy and / or beta Hydroxyalkylamide groups, but especially blocked isocyanate, urethane or methylol ether groups, are used on the other hand. For the preparation of self-crosslinking primary dispersions according to the invention, preference is given to using methylol, methylol ether and N-methylol-N-alkoxymethylamino groups. Furthermore, monomers can be used which are different from the above-described monomers I and the above-described monomers which contain reactive functional groups. These monomers preferably do not contain any reactive functional groups. Apart from monomers (3), these monomers can also serve as the sole monomers.

Examples of suitable monomers which contain reactive functional groups or no reactive functional groups and which are different from the monomers I described above are

(1) Essentially acid-group-free (meth) acrylic esters such as (meth) acrylic or alkyl cycloalkyl esters with up to 20 carbon atoms in the alkyl radical, in particular methyl, ethyl,

Propyl, n-butyl, sec-butyl, tert-butyl, hexyl, ethylhexyl, stearyl and lauryl acrylate or methacrylate; cycloaliphatic (meth) acrylic acid esters, in particular cyclohexyl, isobornyl, dicyclopentadienyl, octahydro-4,7-methano-1H-indene methanol or tert-butylcyclohexyl (meth) acrylate;

(Meth) acrylic acid oxaalkyl esters or oxacycloalkyl esters such as ethyl triglycol (meth) acrylate and methoxy oligoglycol (meth) acrylate with a molecular weight Mn of preferably 550 or other ethoxylated and / or propoxylated hydroxyl group-free (meth) acrylic acid derivatives. These can be found in subordinate

Amounts of higher functional (meth) acrylic acid alkyl or cycloalkyl esters such as ethylene glycol, propylene glycol, diethylene glycol, dipropylene glycol, butylene glycol, pentane-1, 5-diol, hexane-1, 6-diol, octahydro-4,7- methano-1 H-indene-dimethanol or cyclohexane-1,2-, 1,3- or -1,4-diol-di (meth) acrylate; Trimethylolpropane di or

tri (meth) acrylate; or pentaerythritol-di-, -tri- or - Contain tetra (meth) acrylate. In the context of the present invention, minor amounts of higher-functional monomers are understood to mean those amounts which do not lead to crosslinking or gelling of the copolymers.

(2) Monomers which carry at least one hydroxyl group, amino group, alkoxymethylamino group or imino group per molecule and which are essentially free of acid groups, such as hydroxyalkyl esters of acrylic acid, methacrylic acid or another alpha-beta-olefinically unsaturated carboxylic acid which are derived from an alkylene glycol and which the acid is esterified, or which can be obtained by reacting the alpha, beta-olefinically unsaturated carboxylic acid with an alkylene oxide, in particular hydroxyalkyl esters of acrylic acid, methacrylic acid, ethacrylic acid,

Crotonic acid, maleic acid, fumaric acid or itaconic acid in which the hydroxyalkyl group contains up to 20 carbon atoms, such as 2-hydroxyethyl, 2-hydroxypropyl, 3-hydroxypropyl, 3-hydroxybutyl, 4-hydroxybutyl acrylate, methacrylate, ethacrylate, crotonate, maleinate, fumarate or itaconate; or hydroxycycloalkyl esters such as

1,4-bis (hydroxymethyl) cyclohexane, octahydro-4,7-methano-1 H-indene-dimethanol or methyl propanediol monoacrylate, monomethacrylate, monoethacrylate, monocrotonate, monomaleinate, monofumarate or monoitaconate; or reaction products from cyclic esters, e.g. epsilon-caprolactone and this

Hydroxyalkyl or cycloalkyl esters; or olefinically unsaturated alcohols such as allyl alcohol or polyols such as trimethylolpropane mono- or diallyl ether or pentaerythritol mono-, di- or triallyl ether (with regard to these higher-functional monomers (2) the same applies analogously to the higher-functional monomers (1));

Aminoethyl acrylate, aminoethyl methacrylate, allylamine or N- Methyliminoethyl acrylate or N, N-

Di (methoxymethyl) aminoethyl acrylate and methacrylate or N, N-di (butoxymethyl) aminopropyl acrylate and methacrylate;

(3) monomers which carry at least one acid group which can be converted into the corresponding acid anion group per molecule, such as acrylic acid, methacrylic acid, ethacrylic acid, crotonic acid, maleic acid, fumaric acid or itaconic acid; olefinically unsaturated sulfonic or phosphonic acids or their partial esters; or maleic acid mono (meth) acryloyloxyethyl ester, succinic acid mono (meth) acryloyloxyethyl ester or phthalic acid mono (meth) acryloyloxyethyl ester. In the context of the present invention, the monomers (3) are preferably not used as the sole monomers, but always in conjunction with other monomers and only in such small amounts that the monomers (3) do not polymerize outside the droplets of the miniemulsion.

(4) vinyl esters of alpha-branched monocarboxylic acids with 5 to 18 carbon atoms in the molecule. The branched

Monocarboxylic acids can be obtained by reacting

Formic acid or carbon monoxide and water with olefins in

Presence of a liquid, strongly acidic catalyst; the olefins can be cracked products of paraffinic hydrocarbons, such as mineral oil fractions, and can contain both branched and straight-chain acyclic and / or cycloaliphatic olefins.

In the implementation of such olefins with formic acid or with

Carbon monoxide and water form a mixture

Carboxylic acids in which the carboxyl groups are predominantly located on a quaternary carbon atom. Other olefinic

Starting materials are propylene trimer, propylene tetramer and Diisobutylene. The vinyl esters (4) can, however, also be prepared from the acids in a manner known per se, for example by allowing the acid to react with acetylene. Because of the good availability, particular preference is given to vinyl esters of saturated aliphatic monocarboxylic acids having 9 to 11 carbon atoms which are branched on the alpha carbon atom, but in particular VersaticΘ acids (cf. Römpp Lexikon Lacke und Druckfarben, Georg Thieme Verlag, Stuttgart, New York, 1998, "Versatic® acids", pages 605 and 606).

(5) reaction products of acrylic acid and / or methacrylic acid with the glycidyl ester of a monocarboxylic acid with 5 to 18 C atoms per molecule branched in the alpha position, in particular one Versatic® acid, or instead of the reaction product an equivalent amount of acrylic and / or methacrylic acid, which is then reacted during or after the polymerization reaction with the glycidyl ester of a monocarboxylic acid having 5 to 18 carbon atoms per molecule, in particular a Versatic® acid, which is branched in the alpha position.

(6) Cyclic and / or acyclic olefins such as ethylene, propylene, but-1-ene, pent-1-ene, hex-1-ene, cyclohexene, cyclopentene, norbornene, butadiene, isoprene, cyclopentadiene and / or dicyclopentadiene.

(7) (meth) acrylic acid amides such as (meth) acrylic acid amide, N-methyl, N-ethyl, N-propyl, N-butyl, N-cyclohexyl, and / or N-methylol, N, N- Dimethylol, N-methoxymethyl, N, N-di (methoxymethyl), N-ethoxymethyl and / or N, N-di (ethoxyethyl) - (meth) acrylic acid amide; (8) monomers containing epoxy groups, such as the glycidyl ester of acrylic acid, methacrylic acid, ethacrylic acid, crotonic acid,

Maleic acid, fumaric acid and / or itaconic acid.

(9) vinyl aromatic hydrocarbons such as styrene, alpha-alkylstyrenes, in particular alpha-methylstyrene, and / or vinyltoluene; Vinylbenzoic acid (all isomers), N, N-diethylaminostyrene (all isomers), alpha-methylvinylbenzoic acid (all isomers), N, N-diethylamino-alpha-methylstyrene (all isomers) and / or p-vinylbenzenesulfonic acid.

(10) nitriles such as acrylonitrile and / or methacrylonitrile.

(11) vinyl compounds, in particular vinyl and / or vinylidene dihalides such as vinyl chloride, vinyl fluoride,

Vinylidene dichloride or vinylidene difluoride; N-vinylamides such as vinyl-N-methylformamide, N-vinylcaprolactam, 1-vinylimidazole or N-vinylpyrrolidone; Vinyl ethers such as ethyl vinyl ether, n-propyl vinyl ether, isopropyl vinyl ether, n-butyl vinyl ether, isobutyl vinyl ether and / or vinyl cyclohexyl ether; and / or vinyl esters such as vinyl acetate,

Vinyl propionate, vinyl butyrate, vinyl pivalate and / or the vinyl ester of 2-methyl-2-ethylheptanoic acid.

(12) Allyl compounds, especially allyl ethers and esters such as allyl methyl, ethyl, propyl or butyl ether or allyl acetate, propionate or butyrate.

(13) Acryloxysilane-containing vinyl monomers, which can be prepared by reacting hydroxy-functional silanes with epichlorohydrin and then reacting the reaction product with (Meth) acrylic acid and / or hydroxyalkyl and / or cycloalkyl esters of (meth) acrylic acid (cf. monomers a2) and / or

(14) polysiloxane macromonomers which have a number average molecular weight Mn of 1,000 to 40,000 and an average of 0.5 to 2.5 ethylenically unsaturated double bonds per molecule; in particular polysiloxane macromonomers which have a number average molecular weight Mn of 2,000 to 20,000, particularly preferably 2,500 to 10,000 and in particular 3,000 to 7,000 and on average 0.5 to 2.5, preferably 0.5 to 1.5, ethylenically unsaturated

Have double bonds per molecule as described in DE 38 07 571 A1 on pages 5 to 7, DE 37 06 095 A1 in columns 3 to 7, EP 0 358 153 B1 on pages 3 to 6, in US 4,754,014 A1 in columns 5 to 9, in DE 44 21 823 A1 or in international patent application WO 92/22615

Page 12, line 18, to page 18, line 10.

Further examples of suitable monomers can be found in German patent application DE 196 28 142 A1, page 2, line 50, to page 3, line 7.

The monomers are preferably selected so that (meth) acrylate copolymers result whose profile of properties is primarily determined by the (meth) acrylates described above. Vinylaromatic hydrocarbons (9), in particular styrene, are then preferably used as comonomers.

The monomers described above are converted into copolymers in the presence of at least one water- and / or oil-soluble initiator which forms free radicals. As examples of usable

Initiators are called: dialkyl peroxides, such as di-tert-butyl peroxide or dicumyl peroxide; Hydroperoxides, such as cumene hydroperoxide or tert-butyl hydroperoxide; Peresters, such as tert-butyl perbenzoate, tert-butyl perpivalate, tert-butyl per-3,5,5-trimethylhexanoate or tert-butyl per-2-ethylhexanoate; Peroxodicarbonates such as bis (4-tert-butylcyclohexyl) peroxodicarbonate; Potassium, sodium or

ammonium peroxodisulfate; Azo initiators, for example azo dinitriles such as azobisisobutyronitrile; C-C-cleaving initiators such as benzpinacol silyl ether; or a combination of a non-oxidizing initiator with hydrogen peroxide. Further examples of suitable initiators are described in German patent application DE 196 28 142 A1, page 3, line 49, to page 4, line 6. Combinations of these initiators can also be used.

Comparatively large amounts of radical initiator are preferably added, preferably 1 to 20, preferably 2 to 19, particularly preferably 3 to 18, very particularly preferably 4 to 17 and in particular 5 to 15 parts by weight of at least one initiator being used per 100 parts by weight of monomers.

The monomers described above are polymerized or copolymerized in the presence of at least one hydrophobic additive.

The property "hydrophobic" is to be understood as the constitutional property of a molecule or a functional group to behave exophilically towards water, ie it shows the tendency not to penetrate water or to leave the aqueous phase. In addition, reference is made to Römpp Lexikon Lacke und Druckfarben, Georg Thieme Verlag, Stuttgart, New York, 1998, "Hydrophilie", "Hydrophobie", pages 294 and 295. The hydrophobic additives are preferably selected from the group consisting of

(1) at least one hydrophobic crosslinking agent for the (co) polymer of the invention resulting from the monomers

Primary dispersion;

(2) at least one polyhydroxy-functionalized cyclic and acyclic alkane with 9 to 16 carbon atoms in the molecule and

(3) at least one hydrophobic compound selected from the group consisting of esters of 3 to 6 carbon atoms containing alpha.beta-monoolefinically unsaturated carboxylic acids with alcohols with 12 to 30 carbon atoms in the alkyl radical; Esters of vinyl and / or allyl alcohol with 12 to 30

Alkane monocarboxylic, sulfonic and / or phosphonic acids having carbon atoms in the molecule; Amides of 3 to 6 carbon atoms containing alpha.beta-monoolefinically unsaturated carboxylic acids with alkylamines with 12 to 30 carbon atoms in the alkyl radical; Macromomers based on olefinically unsaturated compounds with an average of at least one, in particular terminal, olefinically unsaturated group in the molecule; Polysiloxane macromonomers with an average of at least one, in particular terminal, olefinically unsaturated group in the molecule; oligomeric and / or polymeric polymerization, polycondensation and / or polyaddition products; water

Molecular weight regulators, especially mercaptans; aliphatic, cycloaliphatic and / or aromatic halogenated and / or non-halogenated hydrocarbons;

Alkanols and / or alkylamines with at least 12 Carbon atoms in the alkyl radical; Organosilanes and / or - siloxanes; vegetable, animal, semi-synthetic and / or synthetic oils; and / or hydrophobic dyes;

selected, of which the hydrophobic crosslinking agents and the polyhydroxy-functionalized cyclic and acyclic alkanes having 9 to 16 carbon atoms in the molecule are advantageous and are therefore used with preference.

The monomers are particularly preferably polymerized in the presence of at least one hydrophobic crosslinking agent (co) which contains the above-described reactive functional groups (b) or (a) which, with the complementary reactive functional groups present in the resulting (co) polymers (a ) or (b) crosslinking reactions. The resulting primary dispersions according to the invention and the coating materials, adhesives and sealants according to the invention produced therefrom contain the crosslinking agents in a particularly good distribution, which is why the crosslinking reactions proceed particularly well, so that fewer crosslinking agents can be used than in the coating materials, adhesives and sealants which are used according to the processes of the prior art of technology have been manufactured.

Examples of particularly suitable hydrophobic crosslinking agents are blocked polyisocyanates, tris (alkoxycarbonylamino) triazines or completely etherified aminoplast resins.

Examples of suitable blocking agents for the preparation of the blocked polyisocyanates are the blocking agents known from US Pat. No. 4,444,954 A: i) phenols such as phenol, cresol, xylenol, nitrophenol, chlorophenol, ethylphenol, t-butylphenol, hydroxybenzoic acid, esters of this acid or 2,5-di-tert-butyl-4-hydroxytoluene;

ii) lactams, such as ε-caprolactam, δ-valerolactam, γ-butyrolactam or ß-propiolactam;

iii) active methylenic compounds such as diethyl malonate, dimethyl malonate, ethyl or methyl acetoacetate or acetylacetone;

iv) alcohols such as methanol, ethanol, n-propanol, isopropanol, n-butanol, isobutanol, t-butanol, n-amyl alcohol, t-amyl alcohol, lauryl alcohol, ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, ethylene glycol monopropyl ether,

Ethylene glycol monobutyl ether, diethylene glycol monomethyl ether, diethylene glycol monoethyl ether, propylene glycol monomethyl ether, methoxymethanol, glycolic acid, glycolic acid ester, lactic acid, lactic acid ester, methylolurea, methylolmelamine, diacetone alcohol, ethylene chlorohydrin, ethylene bromohydrin, 1, 3-

Dichloro-2-propanol, 1, 4-cyclohexyldimethanol or

acetone cyanohydrin;

v) mercaptans such as butyl mercaptan, hexyl mercaptan, t-butyl mercaptan, t-dodecyl mercaptan, 2-mercaptobenzothiazole,

Thiophenol, methylthiophenol or ethylthiophenol;

vi) acid amides such as acetoanilide, acetoanisidinamide, acrylamide, methacrylamide, acetic acid amide, stearic acid amide or benzamide;

vii) imides such as succinimide, phthalimide or maleimide; viii) amines such as diphenylamine, phenylnaphthylamine, xylidine, N-phenylxylidine, carbazole, aniline, naphthylamine, butylamine, dibutylamine or butylphenylamine;

ix) imidazoles such as imidazole or 2-ethylimidazole;

x) ureas such as urea, thiourea, ethylene urea, ethylene thiourea or 1,3-diphenylurea;

xi) carbamates such as phenyl N-phenylcarbamate or 2-

oxazolidone;

xii) imines such as ethyleneimine;

xiii) oximes such as acetone oxime, formal doxime, acetaldoxime, acetoxime,

Methyl ethyl ketoxime, diisobutyl ketoxime, diacetyl monoxime,

Benzophenone oxime or chlorohexanone oximes;

xiv) salts of sulfurous acid such as sodium bisulfite or potassium bisulfite;

xv) hydroxamic acid esters such as benzyl methacrylohydroxamate (BMH) or

allyl methacrylohydroxamate; or

xvi) substituted pyrazoles, in particular dimethylpyrazole, or

triazoles; such as

xvii) mixtures of these blocking agents, in particular dimethylpyrazole and triazoles, malonic esters and acetoacetic acid esters or

Dimethylpyrazole and succinimide. Examples of suitable organic polyisocyanates to be blocked are in particular the so-called lacquer polyisocyanates with aliphatic, cycloaliphatic, araliphatic and / or aromatically bound isocyanate groups. Polyisocyanates having 2 to 5 isocyanate groups per molecule and having viscosities of 100 to 10,000, preferably 100 to 5000, are preferred.

Examples of suitable polyisocyanates to be blocked are polyisocyanates containing isocyanurate, biuret, allophanate, iminooxadiazinedione, urethane, urea and / or uretdione groups. Polyisocyanates containing urethane groups are obtained, for example, by reacting some of the isocyanate groups with polyols, e.g. Trimethylolpropane and glycerin.

For the preparation of the polyisocyanates to be blocked, preference is given to aliphatic or cycloaliphatic diisocyanates, in particular hexamethylene diisocyanate, isophorone diisocyanate,

Dicyclohexylmethane-2,4'-diisocyanate, dicyclohexylmethane-4,4'-diisocyanate, diisocyanates derived from dimer fatty acids, as marketed by Henkel under the trade name DDI 1410 and in the patents WO 97/49745 and WO 97 / 49747 describes in particular 2-heptyl-3,4-bis (9-isocyanatononyl) -1-pentyl-cyclohexane; or 1, 2-, 1,4- or 1,3-bis (isocyanatomethyl) cyclohexane, 1,2-, 1, 4- or 1, 3-bis (2-isocyanatoeth-1-yl) cyclohexane, 1, 3 - bis (3-isocyanatoprop-1-yl) cyclohexane or 1, 2-, 1, 4- or 1, 3-bis (4-isocyanatobut-1-yl) cyclohexane, 1, 8-diisocyanato-4-isocyanatomethyl-octane , 1, 7-

Diisocyanato-4-isocyanatomethyl-heptane or 1-isocyanato-2- (3-isocyanatopropyl) cyclohexane or mixtures thereof. As such, the diisocyanates can also be used to prepare blocked diisocyanates. However, they are preferably not used alone, but in a mixture with the polyisocyanates.

Mixtures of polyisocyanates based on hexamethylene diisocyanate and containing uretdione and / or isocyanurate groups and / or allophanate groups, as are formed by catalytic oligomerization of hexamethylene diisocyanate using suitable catalysts, are very particularly preferably used.

Examples of particularly suitable fully etherified aminoplast resins are melamine resins, guanamine resins or urea resins. Any aminoplast resin suitable for clearcoats or a mixture of such aminoplast resins can be used here. In addition, Römpp Lexikon Lacke und Druckfarben, Georg Thieme Verlag, 1998, page 29, "Aminoharze", and the textbook "Lackadditive" by Johan Bieleman, Wiley-VCH, Weinheim, New York, 1998, pages 242 ff., Or on the book "Paints, Coatings and Solvents", second completely revised edition, Edit. D. Stoye and W. Freitag, Wiley-VCH, Weinheim, New York, 1998, pages 80 ff. Furthermore, the usual and known aminoplast resins come into consideration, the methylol and / or methoxymethyl groups z. T. are defunctionalized by means of carbamate or allophanate groups.

Crosslinking agents of this type are described in the patents US 4,710,542 A1 and EP 0 245 700 B1 as well as in the article by B. Singh and co-workers "Carbamylmethylated Melamines, Novel Crosslinkers for the Coatings Industry" in Advanced Organic Coatings Science and Technology Series, 1991, volume 13, pages 193 to 207.

The particularly suitable tris (alkoxycarbonylamino) triazines had the following formula:

II

0

Examples of particularly suitable tris (alkoxycarbonylamino) triazines are described in the patents US 4,939,213 A, US 5,084,541 A or EP 0 624 577 A1. In particular, the tris (methoxy-, tris (butoxy- and / or tris (2-ethylhexoxycarbonylamino) triazines are used.

The methyl-butyl mixed esters, the butyl-2-ethylhexyl mixed esters and the butyl esters are advantageous. Compared to the pure methyl ester, these have the advantage of better solubility in polymer melts and also have less tendency to crystallize out.

Of the crosslinking agents described above, the blocked polyisocyanates offer particular advantages and are therefore used with very particular preference in accordance with the invention.

In the process according to the invention, the ratio of the monomers which contain complementary reactive functional groups (a) or (b) to the crosslinking agents can vary very widely. According to the invention, it is advantageous if the molar ratio of complementary reactive functional groups (a) or (b) in the Copolymers to complementary reactive functional groups (a) or (b) in the crosslinking agents at 5.0: 1.0 to 1.0: 5.0, preferably 4.0: 1.0 to 1.0: 4.0, more preferably 3.0: 1.0 to 1.0: 3.0 and in particular 2.0: 1 to 1: 2.0. Particular advantages result if the molar ratio is approximately or exactly 1.0: 1.0.

In addition, the ratio of the total amount of monomers to the hydrophobic crosslinking agents can vary very widely. According to the invention it is advantageous if 20 to 200, preferably 40 to 160, particularly preferably 60 to 140, very particularly preferably 80 to 130 and in particular 90 to 120 parts by weight of at least one hydrophobic crosslinking agent are used per 100 parts by weight of monomers.

The functionalized alkanes are derived from branched, cyclic or acyclic alkanes with 9 to 16 carbon atoms, which each form the basic structure.

Examples of suitable alkanes of this type with 9 carbon atoms are 2-methyloctane, 4-methyloctane, 2,3-dimethyl-heptane, 3,4-dimethyl-heptane, 2,6-dimethyl-heptane, 3,5-dimethyl-heptane, 2 -Methyl-4-ethylhexane or isopropylcyclohexane.

Examples of suitable alkanes of this type with 10 carbon atoms are 4-ethyloctane, 2,3,4,5-tetramethyl-hexane, 2,3-diethyl-hexane or 1-methyl-2-n-propyl-cyclohexane.

Examples of suitable alkanes of this type with 11 carbon atoms are 2,4,5,6-tetramethyl-heptane or 3-methyl-6-ethyl-octane. Examples of suitable are alkanes having 12 carbon atoms, 4-methyl-7-ethyl-nonane, 4,5-diethyl-octane, 1 ^{'-ethyl-butyl-cyclohexane,} 3,5-diethyl-octane or 2,4-diethyl- octane.

Examples of suitable alkanes of this type with 13 carbon atoms are 3,4-dimethyl-5-ethyl-nonane or 4,6-dimethyl-5-ethyl-nonane.

An example of a suitable alkane of this type with 14 carbon atoms is 3,4-dimethyl-7-ethyl-decane.

Examples of suitable alkanes of this type with 15 carbon atoms are 3,6-diethyl-undecane or 3,6-dimethyl-9-ethyl-undecane.

Examples of suitable alkanes of this type with 16 carbon atoms are 3,7-diethyl-dodecane or 4-ethyl-6-isopropyl-undecane.

Of these basic structures, the alkanes with 10 to 14 and in particular 12 carbon atoms are particularly advantageous and are therefore used with preference. Of these, the octane derivatives are particularly advantageous.

It is advantageous for the invention if the functionalized alkanes have a boiling point of over 200, preferably 220 and in particular 240 ° C. In addition, they should have a low evaporation rate.

It is advantageous for the coating materials of the invention if the functionalized alkanes are acyclic.

The functionalized alkanes generally have a primary and / or secondary hydroxyl groups. For the invention It is advantageous for coating materials if primary and secondary groups are present in a compound.

Very particularly advantageous coating materials according to the invention are obtained when the diols are positionally isomeric dialkyloctanediols, in particular positionally isomeric diethyloctanediols.

The positionally isomeric diethyloctanediols to be used according to the invention contain a linear Cs-carbon chain.

With regard to the two ethyl groups, the Cs carbon chain has the following substitution pattern: 2.3, 2.4, 2.5, 2.6, 2.7, 3.4, 3.5, 3.6 or 4.5. According to the invention, it is advantageous if the two ethyl groups are in the 2,4-position, i. that is, it is 2,4-diethyloctanediols.

With regard to the two hydroxyl groups, the Cs carbon chain has the following substitution pattern: 1, 2, 1, 3, 1, 4, 1, 5, 1, 6, 1, 7, 1, 8, 2,3, 2,4, 2.5, 2.6, 2.7, 2.8, 3.4, 3.5, 3.6, 3.7, 3.8, 4.5, 4.6, 4.8, 5, 6, 5.7, 5.8, 6.7, 6.8 or 7.8. According to the invention, it is advantageous if the two hydroxyl groups are in the 1, 5-position, ie. that is, it is diethyloctane-1,5-diols.

The two substitution patterns are combined in any way, i. that is, the diethyloctanediols to be used in the present invention

2,3-diethyloctane-1, 2-, -1, 3-, -1, 4-, -1, 5-, -1, 6-, -1, 7-, -1, 8-, -2, 3-, -2.4-, -2.5 -, -2.6-, -2.7-, -2.8-, -3.4-, -3.5-, -3.6- , -3.7-, -3.8 -, -4.5-, -4.6-, -4.7-, -4.8-, - 5.6 -, -5.7-, - 5.8-, -6.7-, -6.8- or -7.8-diol, 2,4-diethyloctane-1, 2-, -1,3-, -1, 4-, -1,5-, -1, 6-, -1,7-, -1, 8-, -2, 3-, -2.4-, -2.5 -, -2.6-, -2.7-, -2.8-, -3.4-, -3.5-, -3.6- , -3.7-, -3.8 -, -4.5-, -4.6-, -4.7-, -4.8-, - 5.6 -, -5.7-, - 5.8-, -6.7-, -6.8- or -7.8-diol,

2,5-diethyloctane-1, 2-, -1, 3-, -1, 4-, -1, 5-, -1, 6-, -1, 7-, -1, 8-, -2, 3-, -2.4-, -2.5 -, -2.6-, -2.7-, -2.8-, -3.4-, -3.5-, -3.6- , -3.7-, -3.8 -, -4.5-, -4.6-, -4.7-, -4.8-, - 5.6 -, -5.7-, - 5.8-, -6.7-, -6.8- or -7.8-diol,

2.6- Diethyloctane-1, 2-, -1, 3-, -1, 4-, -1, 5-, -1, 6-, -1, 7-, -1, 8-, -2,3- , -2.4-, -2.5 -, -2.6-, -2.7-, -2.8-, -3.4-, -3.5-, -3.6-, - 3.7-, -3.8 -, -4.5-, -4.6-, -4.7-, -4.8-, -

5.6 -, -5.7-, -5.8-, -6.7-, -6.8- or -7.8-diol,

2.7- diethyloctane-1, 2-, -1, 3-, -1, 4-, -1, 5-, -1, 6-, -1, 7-, -1, 8-, -2,3- , -2.4-, -2.5 -, -2.6-, -2.7-, -2.8-, -3.4-, -3.5-, -3.6-, - 3.7-, -3.8 -, -4.5-, -4.6-, -4.7-, -4.8-, - 5.6 -, -5.7-, -5, 8-, -6.7-, -6.8- or -7.8-diol,

3,4-diethyloctane-1, 2-, -1, 3-, -1, 4-, -1, 5-, -1, 6-, -1, 7-, -1, 8-, -2, 3-, -2.4-, -2.5 -, -2.6-, -2.7-, -2.8-, -3.4-, -3.5-, -3.6- , -3.7-, -3.8 -, -4.5-, -4.6-, -4.7-, -4.8-, - 5.6 -, -5.7-, - 5.8-, -6.7-, -6.8- or -7.8-diol,

3,5-diethyloctane-1, 2-, -1, 3-, -1, 4-, -1, 5-, -1, 6-, -1, 7-, -1, 8-, -2, 3-, -2.4-, -2.5 -, -2.6-, -2.7-, -2.8-, -3.4-, -3.5-, -3.6- , -3.7-, -3.8 -, -4.5-, -4.6-, -4.7-, -4.8-, - 5.6 -, -5.7-, - 5.8-, -6.7-, -6.8- or -7.8-diol,

3,6-diethyloctane-1, 2-, -1, 3-, -1, 4-, -1, 5-, -1, 6-, -1, 7-, -1, 8-, -2, 3-, -2.4-, -2.5 -, -2.6-, -2.7-, -2.8-, -3.4-, -3.5-, -3.6- , -3.7-, -3.8 -, -4.5-, -4.6-, -4.7-, -4.8-, - 5.6 -, -5.7-, - 5.8-, -6.7-, -6.8- or -7.8-diol or um

4,5-diethyloctane-1, 2-, -1, 3-, -1, 4-, -1, 5-, -1, 6-, -1, 7-, -1, 8-, -2, 3-, -2.4-, -2.5 -, -2.6-, -2.7-, -2.8-, -3.4-, -3.5-, -3.6- , -3.7-, -3.8 -, -4.5-, -4.6-, -4.7-, -4.8-, - 5.6 -, -5.7-, - 5,8-, -6,7-, -6,8- or -7,8-diol. The positionally isomeric diethyloctanediols can be used as individual compounds or as mixtures of two or more diethyloctanediols.

Very special advantages result from the use of 2,4-diethyloctane-1,5-diol.

The preferred positionally isomeric diethyloctanediols are compounds known per se and can be prepared using customary and known synthetic methods in organic chemistry, such as base-catalyzed aldol condensation, or they are obtained as by-products of large-scale chemical syntheses, such as the preparation of 2-ethylhexanol.

The amount of functionalized alkanes which are used in the preparation of the primary dispersions according to the invention can vary very widely and depend on the requirements of the individual case. That is, the upper limit of the amount is primarily that the formation of the microemulsion or miniemulsion is not impeded and / or its stability is not reduced and / or the (co) polymerization of the monomers may not be adversely affected. The amount is limited at the bottom by the fact that so much functionalized alkanes must be used that their technical effects are reliably established. It is advantageous according to the invention if 1 to 30, preferably 2 to 28, particularly preferably 3 to 26, very particularly preferably 4 to 24 and in particular 5 to 22 parts by weight of at least one functionalized alkane are used per 100 parts by weight of monomers.

The monomers described above are also in the presence of at least one oligomeric polyester of a number average Molecular weight of 150 to 1,500, preferably 155 to 1,000, preferably 160 to 800, particularly preferably 165 to 600, very particularly preferably 170 to 400 and in particular 175 to 300 daltons, a hydroxyl number of 100 to 1,000, preferably 150 to 950, preferably 200 to 900, particularly preferably 250 to 850, very particularly preferably 300 to 800 and in particular 350 to 750 mg KOH / g and an acid number <20, preferably <19, preferably <17, particularly preferably <16, very particularly preferably <14 and in particular < 15 mg KOH / g (co) polymerized.

The oligomeric polyesters are preferably branched.

The oligomeric polyesters are produced by the reaction of polyols and polycarboxylic acids and / or their esterifiable derivatives, such as anhydrides and / or esters. The branches are introduced by at least trifunctional compounds selected from the group consisting of polyols, polycarboxylic acids, polycarboxylic acid anhydrides and polycarboxylic acid esters.

Examples of suitable polycarboxylic acids are aromatic, aliphatic and cycloaliphatic polycarboxylic acids. Aromatic and / or aliphatic dicarboxylic acids are preferably used.

Examples of suitable aromatic dicarboxylic acids are phthalic acid, isophthalic acid, terephthalic acid, phthalic acid, isophthalic acid or terephthalic acid monosulfonate, or halophthalic acids such as tetrachloroborus. Tetrabromophthalic acid, of which isophthalic acid is advantageous and is therefore used with preference.

Examples of suitable acyclic aliphatic or unsaturated dicarboxylic acids are oxalic acid, malonic acid, succinic acid, Glutaric acid, adipic acid, pimelic acid, suberic acid, azelaic acid, sebacic acid, undecanedicarboxylic acid or dodecanedicarboxylic acid or maleic acid, fumaric acid or itaconic acid.

Examples of suitable cycloaliphatic and cyclic unsaturated dicarboxylic acids are 1,2-cyclobutanedicarboxylic acid, 1,3-

Cyclobutanedicarboxylic acid, 1, 2-cyclopentanedicarboxylic acid, 1, 3-

Cyclopentanedicarboxylic acid, hexahydrophthalic acid, 1, 3-

Cyclohexanedicarboxylic acid, 1, 4-cyclohexanedicarboxylic acid, 4-methylhexahydrophthalic acid, tricyclodecanedicarboxylic acid,

Tetrahydrophthalic acid or 4-methyltetrahydrophthalic acid. These dicarboxylic acids can be used both in their ice and in their trans form and as a mixture of both forms.

Further examples of suitable dicarboxylic acids are polymeric fatty acids, in particular those with a dimer content of more than 90% by weight, which are also referred to as dimer fatty acids.

The esterifiable derivatives of the above-mentioned dicarboxylic acids, such as e.g. their mono- or polyvalent esters with aliphatic alcohols with 1 to 4 carbon atoms. In addition, the anhydrides of the above-mentioned dicarboxylic acids can also be used if they exist.

If appropriate, monocarboxylic acids can also be used, such as, for example, benzoic acid, tert-butylbenzoic acid, lauric acid, isononanoic acid or fatty acids of naturally occurring oils.

Examples of suitable polyols are diols. Examples of suitable diols are ethylene glycol, 1, 2- or 1, 3-propanediol, 1, 2-, 1, 3- or 1, 4-butanediol, diethylene glycol, dipropylene glycol, 1, 2-, 1, 3-, 1, 4 - or 1, 5-pentanediol, 1, 2-, 1, 3-, 1, 4-, 1, 5- or 1, 6-hexanediol, hydroxypivalic acid neopentyl ester, neopentyl glycol, 1, 2-, 1, 3- or 1, 4- cyclohexanediol, 1, 2-, 1, 3- or 1, 4-cyclohexanedimethanol, trimethylpentanediol, ethyl butyl propanediol, the positionally isomeric diethyl octanediols, 2-butyl-2-ethyl propanediol-1, 3, 2-butyl-2-methyl propane-diol- 1, 3, 2-phenyl-2-methylpropanediol-1, 3, 2-propyl-2-ethylpropanediol-1, 3, 2-di-tert-butylpropanediol-1, 3, 2-butyl-2-propylpropanediol -1, 3, 1-dihydroxymethyl-bicyclo [2.2.1] heptane, 2,2-diethylpropanediol-1,3.

2,2-dipropylpropanediol-1,3,2-cyclo-hexyl-2-methylpropanediol-1,3

2,5-dimethyl-hexanediol-2,5, 2,5-diethylhexanediol-2,5,

2-ethyl-5-methylhexanediol-2,5, 2,4-dimethylpentanediol-2,4,

2,3-dimethylbutanediol-2,3,1,4- (2'-hydroxypropyl) benzene, 1,3- (2'-hydroxypropyl) benzene or the functionalized alkanes described above.

Of these diols, diethylene glycol and neopentyl glycol are particularly advantageous and are therefore used with particular preference.

Examples of suitable at least trifunctional polyols are trimethylolethane, trimethylolpropane, glycerol, pentaerythritol, homopentaerythritol, sorbitol, mannitol, dulcitol, glucitol, erythritol, pyrogallol and resorcinol, especially trimethylolpropane.

Examples of suitable at least trifunctional polycarboxylic acids are benzene tricarboxylic acids, hexane-2,3,5-tricarboxylic acid or naphthalene-1,3,5-tricarboxylic acid or benzene-1,2,4,5-tetracarboxylic acid. Examples of suitable at least trifunctional polycarboxylic acid esters are the esters of the at least trifunctional polycarboxylic acids described above with alcohols having 1 to 4 carbon atoms.

Examples of suitable at least trifunctional

Polycarboxylic anhydrides are the anhydrides of trimellitic acid and benzene-1, 2,4,5-tetracarboxylic acid.

The oligomeric polyesters are prepared by the known methods of esterification, as are described, for example, in German patent application DE 40 24 204 A1, page 4, lines 50 to 65. The reaction is usually carried out at temperatures between 180 and 280 ° C, optionally in the presence of a suitable esterification catalyst, such as e.g. Lithium octoate, dibutyltin oxide, dibutyltin dilaurate or para-toluenesulfonic acid. The heterogeneous esterification catalysts known from German patent application DE 199 07 861 A1 can also be used.

The oligomeric polyester can be prepared in the presence of small amounts of a suitable solvent as an entrainer. As an entrainer z. B. aromatic hydrocarbons, such as in particular xylene and (cyclo) aliphatic hydrocarbons, for. B. cyclohexane or methylcyclohexane used. It is important to ensure that the entraining agents are removed from the oligomeric polyester after production, so that no volatile organic substances are introduced into the primary dispersions according to the invention.

In the method according to the invention, the ratio of

Monomers to oligomeric polyesters vary widely. 1 to 30, preferably 2 to, are preferably used per 100 parts by weight of monomers

28, particularly preferably 3 to 26, very particularly preferably 4 to 24 and in particular 5 to 22 parts by weight of at least one oligomeric polyester applied.

Furthermore, the monomers can be (co) polymerized in the presence of emulsifiers and / or protective colloids. Examples of suitable emulsifiers and / or protective colloids and the amounts in which they are advantageously used can be found in German patent application DE 196 28 142 A1, page 3, lines 8 to 48.

With regard to the molecular weight distribution, the (co) polymers formed from the monomers are not subject to any restrictions. However, the (co) polymerization is advantageously carried out in such a way that a molecular weight distribution Mw / Mn measured with

Gel permeation chromatography using polystyrene as the standard of <10, particularly preferably <7 and in particular <4 results.

If the monomers I are also used, there is yet another additional advantage, namely that the molecular weights of the copolymers can be controlled within wide limits by the choice of the ratio of monomer to monomer I to free radical initiator. In particular, the content of monomer I determines the molecular weight, in such a way that the greater the proportion of monomer I, the lower the molecular weight obtained.

Reactors for the (co) polymerization processes are the customary and known stirred tanks, stirred tank cascades, tubular reactors, loop reactors or Taylor reactors, as described, for example, in the patents DE 198 28 742 A1 or EP 0 498 583 A1 or in the article by K. Kataoka in Chemical Engineering Science, Volume 50, No. 9, 1995, pages 1409 to 1416. The radical copolymerization is preferably carried out in stirred tanks or Taylor reactors, the Taylor reactors being designed so that the conditions of the Taylor flow are met over the entire length of the reactor, even if the kinematic viscosity of the reaction medium changes greatly due to the copolymerization, in particular increases (cf. German patent application DE 198 28 742 A 1).

The (co) polymerization is carried out in an aqueous medium.

The aqueous medium essentially contains water. In addition to the hydrophobic additives described above in detail and, if appropriate, the emulsifiers and / or protective colloids described above, the aqueous medium can also contain the conventional paint additives and / or other dissolved organic and / or inorganic, low and / or high molecular weight substances described in minor amounts included, provided that these do not negatively influence or even inhibit the (co) polymerization and / or cause an emission of volatile organic substances in the coating materials, adhesives and sealants according to the invention. In the context of the present invention, the term “minor amount” is understood to mean an amount which does not cancel out the aqueous character of the aqueous medium.

However, the aqueous medium can also be pure water.

The (co) polymerization is advantageously carried out at temperatures above room temperature, a temperature range from 30 to 95 ° C., very particularly preferably 40 to 90 ° C., being selected. If particularly volatile monomers are used, the (co) polymerization can also be carried out under pressure, preferably under 1.5 to 3000 bar, particularly preferably 5 to 1500 and in particular 10 to 1000 bar. In individual cases, temperatures higher than 95 ° C can be used.

A particular advantage of the method according to the invention proves that it can also be carried out in a batch mode. Otherwise, the procedures described in German patent application DE 196 28 142 A1, page 4, lines 6 to 36 can also be used.

The (co) polymerization is carried out in a micro or mini emulsion, in particular a mini emulsion. The average particle diameter of the emulsified monomer droplets is below 500 nm. It is preferably 10 to 500 nm, preferably 50 to 400 nm and very particularly preferably 100 to 350 nm. The particle diameter is the so-called z-average particle diameter, which is determined by means of photon correlation spectroscopy according to the principle of dynamic, quasi-elastic light scattering. For example, a Coulter N4 Plus Particle Analyzer from Coulter Scientific Instruments or a PCS Malvern Zetasizer 1000 can be used for this. The measurement is usually carried out on an aqueous emulsion which contains 0.01% by weight of the emulsified monomer droplets. The aqueous emulsion also contains the corresponding monomers in dissolved form (until saturation) in the aqueous phase, so that the emulsified monomer droplets do not dissolve.

The preparation of the primary dispersion according to the invention can be carried out so that the bimodal described above Particle size distribution results. Methods for producing bimodal particle size distributions are customary and known in the technological field in question. The seed method described in German patent application DE 196 28 142 A1, page 5, lines 31 to 49 is preferably used.

The production of the mini-emulsions has no special features in terms of method, but takes place in accordance with the customary and known methods of dispersion or emulsification in a high shear field. Examples of suitable processes are described in patent applications DE 196 28 142 A1, page 5, lines 1 to 30, DE 196 28 143 A1, page 7, lines 30 to 58, or EP 0 401 565 A1, lines 27 to 51, described.

In addition to the constituents described above, the primary dispersions according to the invention can also contain at least one additive that is typical of paints.

The paint-typical additives can be added to the primary dispersions according to the invention after, during or before their preparation. It is also possible to combine these measures with one another.

The paint-typical additives from the group consisting of coloring and / or effect-imparting, magnetically shielding, electrically conductive and fluorescent pigments, metal powders, organic and inorganic, transparent and opaque fillers, nanoparticles, organic dyes, crosslinking agents, secondary polyurethane dispersions, such as they are preferred For example, the German patent application DE 199 14 896 A1, column 1, lines 29 to 49, column 1, page 67, to column 2, line 9, column 4, line 23, to column 11, line 5, and column 19, line 12 to column 20, line 65, or in the German patent application DE 44 37 535 A 1, page 2, line 27, to page 6, line 22, and page 7, line 55, to page 8, line 23, UV absorbers, non-regenerable radical scavengers, regenerable radical scavengers, in particular sterically hindered amines (HALS), which, according to the Denisov cycle, scavenge peroxide radicals (cf. Römpp Lexikon Lacke und Druckfarben, Georg Thieme Verlag, Stuttgart, New York, 1998, page 128, “Denisov cycle”), deaerating agents, slip additives, Polymerization inhibitors, catalysts for crosslinking, thermolabile free radical initiators, photoinitiators, thermally curable reactive diluents, reactive diluents curable with actinic radiation, adhesion promoters, leveling agents, film-forming aids, defoamers, emulsifiers, wetting agents and detergents, rheology-thickening additives,

Flame retardants, corrosion inhibitors, waxes and matting agents. These typical coating additives are described, for example, in German patent application DE 199 14 896 A1, column 14, line 6 to column 15, line 9. Suitable crosslinking agents are those described above, including the free polyisocyanates, which are used when the coating material of the invention is formulated as a two-component system.

The color and / or effect, magically shielding, electrically conductive and fluorescent pigments, metal powder and organic and inorganic, opaque fillers are used when the primary dispersions according to the invention or the coating materials produced therefrom as fillers, solid-color topcoats or water-based lacquers, but especially as water-based lacquers in the frame the so-called wet-on-wet process (cf. for example the European patent EP 0 089 497 B1) for the production of color and / or effect multilayer coatings. The other paint-typical additives can both in the invention pigmented as well as in the unpigmented primary dispersions according to the invention or the clearcoats produced therefrom. The primary dispersions according to the invention are also preferably not pigmented in their use as adhesives or sealants or for the production of adhesives or sealants.

If the primary dispersions according to the invention or the coating materials, adhesives and sealants produced therefrom are also to be curable with actinic radiation (dual cure), they contain additives which are curable with actinic radiation. Actinic radiation can be electromagnetic radiation such as near infrared (NIR), visible light, UV light or X-rays, or corpuscular radiation such as electron beams. Examples of suitable additives curable with actinic radiation are known from German patent DE 197 09467 C1.

The primary dispersions according to the invention are stable on storage and do not tend to separate components even after large temperature fluctuations. They can therefore be easily transported over long distances without affecting their advantageous application-related property profile.

In terms of method, the application of the primary dispersions according to the invention has no special features, but can be carried out by all customary application methods, such as spraying, knife coating, brushing, pouring, dipping, trickling or rolling. Spray application methods are preferably used, such as, for example, compressed air spraying, airless spraying, high rotation, electrostatic spray application (ESTA), optionally combined with hot spray application such as, for example, hot air - hot spraying. Suitable substrates are all surfaces to be painted, which are not damaged by curing the paint layers thereon using heat. The substrates preferably consist of metals, plastics, wood, ceramics, stone, textiles, fiber composites, leather, glass, glass fibers, glass and rock wool, mineral and resin-bound building materials, such as gypsum and cement boards or roof tiles, as well as composites of these materials.

Accordingly, the primary dispersions according to the invention or the coating materials, adhesives and sealing compounds produced therefrom, in particular the coating materials, are also outstandingly suitable for applications outside of automotive coating. They come in particular for the painting of buildings indoors and outdoors, the painting of doors, windows and furniture, the industrial painting, including coil coating, container coating and the impregnation and / or coating of electrical components, as well as the painting of white goods , including household appliances, boilers and radiators. In the context of industrial painting, they are suitable for painting practically all parts and objects for private or industrial use such as household appliances, small parts made of metal, such as screws and nuts, hubcaps, rims, packaging, or electrotechnical components such as motor windings or transformer windings.

In the case of electrically conductive substrates, primers can be used which are produced in a customary and known manner from electrocoat materials. Both anodic and cathodic electrocoat materials, but in particular cathodic electrocoat materials, are suitable for this. In the case of non-functionalized and / or non-polar plastic surfaces, these can be in front of the Coating is subjected to a pretreatment in a known manner, such as with a plasma or with flame, or is provided with a hydro primer.

The curing of the applied primary dispersions according to the invention or of the coating materials, adhesives and sealants produced therefrom has no special features in terms of method, but is carried out according to the customary and known thermal methods such as heating in a forced air oven or irradiation with IR lamps, which in the case of Dual Cure can still be supplemented by radiation with actinic radiation. Radiation sources such as high-pressure or low-pressure mercury vapor lamps, which may be doped with lead in order to open a radiation window up to 405 nm, or electron beam sources can be used.

The resulting coatings, adhesive layers and seals according to the invention, in particular the single-layer or multi-layer color and / or effect coatings and clear coatings according to the invention, are simple to produce and have excellent optical properties and high light, chemical and weather resistance. In particular, the paintwork is free of inhomogeneities and has a particularly high gloss and a particularly low haze. Accordingly, the substrates according to the invention which contain at least one coating according to the invention are of a particularly high utility value and a particularly long service life, which makes them economically and technically particularly attractive for manufacturers and users.

Examples

Production Example 1 The production of an oligomeric polyester with a high hydroxyl number

In a steel reactor suitable for polycondensation reactions, 33.409 parts by weight of isophthalic acid, 28.76 parts by weight of neopentyl glycol, 24.792 parts by weight of trimethylolpropane and 13.039 parts by weight of diethylene glycol were condensed in a customary and known manner until an acid number of 10 mg KOH / g was reached. The resulting oligomeric polyester had a hydroxyl number of 583 mg KOH / g and a molecular weight of 233 daltons. The solids content was 100% by weight.

example 1

The preparation of an aqueous primary dispersion

A mixture consisting of 4.3 parts by weight of methyl methacrylate, 5.2 parts by weight of n-butyl acrylate, 2.2 parts by weight of styrene, 4.7 parts by weight of hydroxypropyl methacrylate, 0.5 part by weight of diphenylethylene, 0.5 part by weight of 2,4-diethyloctane-1.5 diol, 0.3 part by weight of Tinuvin® 400 (commercial UV absorber based on triazine from Ciba, 85% in methoxy-2-propanol), 18.2 parts by weight of Crelan® VPLS (blocked with 3,5-dimethylpyrazole aliphatic polyisocyanate based on isophorone diisocyanate), 1.5 parts by weight of the oligomeric polyester of preparation example 1 and 2.3 parts by weight of di (4-tert-butylcyclohexyl) peroxodicarbonate, was treated at room temperature with 58.4 parts by weight of deionized water, the 1 Parts by weight of ammonium nonylphenyl ether sulfate (30% in water, Abex ® EP 110), added and homogenized for 40 seconds with an Ultraturrax at 10,000 rpm. The resulting pre-emulsion was converted into a stable miniemulsion with a z-average particle size, measured by means of photon correlation spectroscopy (PCS Malvern Zetasizer 1000), of <230 nm by means of a pressure release homogenization using a nozzle jet disperser from Wagner at 180 bar. The miniemulsion was transferred to a suitable steel reactor with stirrer and reflux condenser and polymerized at a constant polymerization temperature of 70 ° C. with stirring until the theoretical solids content of 40% by weight was reached. The residual monomer content was then <0.1% by weight. No exothermic reaction could be observed by comparing the oil temperature (heating medium of the reactor) with the temperature of the reaction mixture.

Example 2

The production of a clear lacquer according to the invention

97.56 parts by weight of the aqueous primary dispersion of Example 1 were placed in a stirred kettle. 1.46 parts by weight of a thickener (Collacral® VL, 30% strength aqueous solution of an N-vinylpyrrolidone copolymer) and 0.98 parts by weight of a wetting agent (Byk® 348, polyethermodified.es polydimethylsiloxane) were added with stirring in succession. The resulting clearcoat was stable on storage and showed no segregation even after storage for several months.

Example 3

The production of a multi-layer coating according to the invention

On steel panels coated with a commercially available electrocoat (electrocoat with a layer thickness of 18 - 22 μm) a commercially available aqueous polyurethane-based filler from BASF Coatings AG was first applied and baked with a cup gun. A filler coating with a layer thickness of 35 to 40 μm resulted. A commercially available aqueous black uni base coat from BASF Coatings AG was then applied in the same way to the filler coating and predried at 80 ° C. for 10 minutes. After the panels had been cooled, a layer of the clearcoat material of Example 2 according to the invention was applied using a pneumatic spray gun. The resulting clearcoat films were predried at 50 ° C. for 10 minutes and then cured together with the basecoat films at 130 ° C. object temperature for 25 minutes. The result was basecoats with a thickness of 12 to 15 μm and clear coatings with a thickness of 40 to 50 μm. The black uni base coat was chosen because the best way to observe the formation of surface defects and film defects was on the corresponding test panels.

The multi-layer coating according to the invention had an excellent overall optical impression. The gloss measured according to DIN 67530 using a BYK reflectometer at an angle of 20 ° was 89, the haze 30 to 40.

Claims

claims

1. Volatile organic substances essentially or completely free aqueous primary dispersion containing dispersed and / or emulsified, solid and / or liquid polymer particles and / or dispersed solid core-shell particles with a particle diameter <500 nm, which can be prepared by radical micro- or miniemulsion polymerization at least one olefinically unsaturated monomer in the presence of at least one hydrophobic additive and at least one oligomeric

Polyesters with a number average molecular weight of 150 to 1,500 daltons, a hydroxyl number of 100 to 1,000 mg KOH / g and an acid number <20 mg KOH / g.

2. Aqueous primary dispersion according to claim 1, characterized in that at least two different monomers are copolymerized.

3. Aqueous primary dispersion according to claim 2, characterized in that the monomers are copolymerized by the controlled radical micro- or miniemulsion polymerization.

4. Aqueous primary dispersion according to claim 3, characterized in that one of the monomers from the group consisting of monomers of the general formula I. R ¹ R ² C = CR ³ R ⁴ (I),

wherein the radicals R ¹ , R ² , R ³ and R ^{4 are} each independently of one another 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 R ¹ , R ² , R ³ and R ^{4 are} substituted or unsubstituted aryl, Arylalkyl or arylcycloalkyl radicals, in particular substituted or unsubstituted

Aryl residues, stand; to be selected.

5. Aqueous primary dispersion according to claim 4, characterized in that the aryl radicals R ¹ , R ² , R ³ and / or R ^{4 of} the monomers I are phenyl or naphthyl radicals.

6. Aqueous primary dispersion according to claim 5, characterized in that it is phenyl radicals.

7. Aqueous primary dispersion according to one of claims 2 to 4, characterized in that the substituents in the radicals R ¹ , R ² , R ³ and / or R ^{4 of} the monomers I from the group consisting of electron-withdrawing or electron-donating atoms or organic radicals , to be selected.

8. Aqueous primary dispersion according to claim 5, characterized in that the substituents from the group consisting of halogen atoms, nitrile, nitro, partially or completely halogenated alkyl, cycloalkyl, alkylcycloalkyl, cycloalkylalkyl, aryl, alkylaryl, Cycloalkylaryl, arylalkyl and arylcycloalkyl radicals;

Aryloxy, alkyloxy and cycloalkyloxy radicals; Arylthio, alkylthio and Cycloalkylthio residues and primary, secondary and / or tertiary amino groups can be selected.

9. Aqueous primary dispersion according to one of claims 1 to 8, characterized in that the monomer or that of the

Monomers I various monomers from the group consisting of

(1) substantially acid group-free (meth) acrylic acid esters;

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

(3) monomers which carry at least one acid group which can be converted into the corresponding acid anion group per molecule;

(4) vinyl esters of branches branched in the alpha position

Monocarboxylic acids with 5 to 18 carbon atoms in the molecule;

(5) reaction products of acrylic acid and / or methacrylic acid with the glycidyl ester of a monocarboxylic acid branched in the alpha position with 5 to 18 carbon atoms per molecule;

(6) cyclic and / or acyclic olefins;

(7) (meth) acrylic acid amides; (8) monomers containing epoxy groups;

(9) vinyl aromatic hydrocarbons;

(10) nitriles;

(11) vinyl compounds, in particular vinyl and / or vinylidene dihalides, N-vinylpyrrolidone, vinyl ethers and / or vinyl esters;

(12) allyl compounds, especially allyl ethers and esters;

(13) vinyl monomers containing acryloxysilane, which can be prepared by reacting hydroxy-functional silanes with epichlorohydrin and then reacting the reaction product with methacrylic acid and / or hydroxyalkyl esters of (meth) acrylic acid; and

(14) polysiloxane macromonomers, which are number average

Molecular weight Mn from 1,000 to 40,000 and on average 0.5 to 2.5 ethylenically unsaturated double bonds per molecule;

is selected or will be provided that the

Monomers (3) cannot be used as the sole monomers

10. Aqueous primary dispersion according to one of claims 1 to 9, characterized in that it is in the dispersed

Particles around core-shell particles with cores made of organic Solids and with shells made of copolymers which contain at least one monomer (3) and at least one monomer different therefrom in copolymerized form.

11. Aqueous primary dispersion according to one of claims 1 to 10, characterized in that the hydrophobic additives from the group consisting of

(1) at least one hydrophobic crosslinking agent for the (co) polymer of the aqueous primary dispersion resulting from the monomers;

(3) at least one polyhydroxy-functionalized cyclic and acyclic alkane with 9 to 16 carbon atoms in the molecule and

(3) at least one hydrophobic compound selected from the group consisting of esters of 3 to 6 carbon atoms containing alpha.beta-monoolefinically unsaturated carboxylic acids with alcohols with 12 to 30

Carbon atoms in the alkyl radical; Esters of vinyl and / or allyl alcohol with 12 to 30 carbon atoms in the molecule having alkane monocarboxylic, sulfonic and / or phosphonic acids; Alpha.beta-monoolefinically unsaturated amides of 3 to 6 carbon atoms

Carboxylic acids with alkylamines with 12 to 30 carbon atoms in the alkyl radical; Macromomers based on olefinically unsaturated compounds with an average of at least one, in particular terminal, olefinically unsaturated group in the molecule;

Polysiloxane macromonomers with a statistical average at least one, especially terminal, olefinically unsaturated group in the molecule; oligomeric and / or polymeric polymerization, polycondensation and / or polyaddition products; water-insoluble molecular weight regulators, especially mercaptans; aliphatic, cycloaliphatic and / or aromatic halogenated and / or non-halogenated

hydrocarbons; Alkanols and / or alkylamines with at least 12 carbon atoms in the alkyl radical; Organosilanes and / or siloxanes; vegetable, animal, semi-synthetic and synthetic oils; and hydrophobic dyes;

to be selected.

12. Aqueous primary dispersion according to claim 11, characterized in that at least one additive from the group consisting of the crosslinking agent and the polyhydroxy-functionalized cyclic and acyclic alkanes with 9 to 16 carbon atoms in the molecule is used.

13. Aqueous primary dispersion according to claim 11 or 12, characterized in that the hydrophobic crosslinking agents from the group consisting of blocked polyisocyanates, tris (alkoxycarbonylamino) triazines and completely etherified

Aminoplast resins can be selected.

14. Aqueous primary dispersion according to one of claims 1 to 13, characterized in that one uses a branched polyester.

15. Aqueous primary dispersion according to claim 14, characterized in that the branches via at least one at least trifunctional compound selected from the group consisting of polyols, polycarboxylic acids, polycarboxylic acid anhydrides and polycarboxylic acid esters in the

Introduces polyester.

16. Aqueous primary dispersion according to claim 15, characterized in that trimethylol propane is used.

17. Coating material according to one of claims 1 to 16, characterized in that it contains at least one paint-typical additive selected from the group consisting of color and / or effect, magnetically shielding, electrically conductive and fluorescent pigments, metal powders, organic and inorganic, transparent and opaque fillers, nanoparticles, crosslinking agents, secondary aqueous polyurethane dispersions, UV absorbers, regenerable and non-regenerable radical scavengers, deaerating agents, slip additives, polymerization inhibitors, catalysts for the

Cross-linking, thermolabile radical initiators,

Photoinitiators, thermally curable reactive diluents, reactive diluents curable with actinic radiation, adhesion promoters, flow control agents, film-forming aids, defoamers, emulsifiers, wetting agents and detergents, rheology control agents

Contains additives (thickeners), flame retardants, corrosion inhibitors, waxes and matting agents.

18. A process for the preparation of an aqueous primary dispersion which is substantially or completely free of volatile organic substances according to one of claims 1 to 17, characterized in that that at least one olefinically unsaturated monomer in the presence of at least one hydrophobic additive and at least one oligomeric polyester having a number average molecular weight of 150 to 1,500 daltons, a hydroxyl number of 100 to 1,000 mg KOH / g and an acid number <20 mg KOH / g by radical micro - or miniemulsion polymerization (co) polymerized.

19. Use of the aqueous primary dispersion according to one of claims 1 to 16 and / or of the aqueous primary dispersion prepared according to claim 18 as a coating material, adhesive or

Sealant or for the manufacture of a broom sealant, an adhesive or a sealant.

20. Use according to claim 19, characterized in that the coating material for the automotive painting, the painting of buildings indoors and outdoors, the painting of doors, windows and furniture, industrial painting, including coil coating, container coating and impregnation and / or coating of electrical components, as well as the coating of white goods, including household appliances, boilers and radiators.

21. Use according to claim 20, characterized in that the coating material is used as a clear lacquer or as a water-based lacquer.

22. Use according to claim 20 or 21, characterized in that the coating material is used to produce color and / or effect multi-layer coatings.