Classifications

• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F283/00—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
  • C09D151/00—Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers
  • C09D151/08—Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers grafted on to macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F283/00—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G
  • C08F283/006—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G on to polymers provided for in C08G18/00
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G18/00—Polymeric products of isocyanates or isothiocyanates
  • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
  • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
  • C08G18/40—High-molecular-weight compounds
  • C08G18/42—Polycondensates having carboxylic or carbonic ester groups in the main chain
  • C08G18/4205—Polycondensates having carboxylic or carbonic ester groups in the main chain containing cyclic groups
  • C08G18/423—Polycondensates having carboxylic or carbonic ester groups in the main chain containing cyclic groups containing cycloaliphatic groups
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G18/00—Polymeric products of isocyanates or isothiocyanates
  • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
  • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
  • C08G18/40—High-molecular-weight compounds
  • C08G18/42—Polycondensates having carboxylic or carbonic ester groups in the main chain
  • C08G18/44—Polycarbonates
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G18/00—Polymeric products of isocyanates or isothiocyanates
  • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
  • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
  • C08G18/65—Low-molecular-weight compounds having active hydrogen with high-molecular-weight compounds having active hydrogen
  • C08G18/66—Compounds of groups C08G18/42, C08G18/48, or C08G18/52
  • C08G18/6633—Compounds of group C08G18/42
  • C08G18/6659—Compounds of group C08G18/42 with compounds of group C08G18/34
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G18/00—Polymeric products of isocyanates or isothiocyanates
  • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
  • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
  • C08G18/65—Low-molecular-weight compounds having active hydrogen with high-molecular-weight compounds having active hydrogen
  • C08G18/66—Compounds of groups C08G18/42, C08G18/48, or C08G18/52
  • C08G18/6666—Compounds of group C08G18/48 or C08G18/52
  • C08G18/667—Compounds of group C08G18/48 or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38
  • C08G18/6674—Compounds of group C08G18/48 or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38 with compounds of group C08G18/3203
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L75/00—Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
  • C08L75/04—Polyurethanes
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
  • C09D175/00—Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
  • C09D175/04—Polyurethanes

Definitions

• the invention relates to aqueous polyurethane (PUR) polyacrylate (PAC) hybrid self-contained dispersions and the aqueous two-component (2K) coating compositions produced therefrom, a process for their production and use.
• PUR polyurethane
• PAC polyacrylate
• Aqueous coating systems based on polyurethane-polyacrylate hybrid dispersions are already known and widely used in the paint industry.
• the advantage of the physical blend ("blend") over separately produced polyurethane and polyacrylate dispersions is that the hybrid dispersions synergistically combine the positive properties of polyurethane dispersions with those of polyacrylate dispersions.
• the polyurethane-polyacrylate hybrid dispersions are prepared by emulsion polymerizing a vinyl polymer (“polyacrylate”) in an aqueous polyurethane dispersion.
• polyacrylate vinyl polymer
• second dispersions is understood to mean those aqueous dispersions which are first polymerized in the homogeneous organic medium and are then redispersed in the aqueous medium under neutralization, generally without the addition of external emulsifiers.
• WO-A 95/16004 describes, for example, water-borne paint binders based on oligourethane-acrylate copolymers.
• a monomer mixture of vinylically unsaturated monomers is radically polymerized in a water-dilutable organic solvent and in the presence of a water-soluble oligourethane with a molecular weight of 750 to 1000. This secondary dispersion is then used to formulate stoving lacquers.
• DE-A 40 10 176 discloses oxidatively drying lacquers, a polymer being used as the binder, which polymer can be obtained by polymerizing 25 polymeric double bonds in an organic solvent (A) with ethylenically unsaturated monomers in the presence (B) of a polyurethane resin contains, are polymerized.
• EP-A 657 483 describes aqueous two-component coating compositions consisting of a polyisocyanate component and an aqueous polyurethane dispersion as the polyol component.
• the polyol component is produced by neutralization and dispersion of unsaturated poly-urethane mal-isomers which are hydrophilized with acid groups and contain lateral and / or terminal vinyl groups. These PUR macromers are then radically polymerized in the aqueous phase, if appropriate after adding further vinyl monomers.
• EP-A 742 239 discloses two-component coating systems based on polyisocyanate crosslinkers and aqueous hydroxy-terminated polyurethane prepolymer / acrylic hybrids.
• hybrid polymers are obtained by converting a water-dispersible NCO-functional urethane prepolymer with at least one hydroxy-functional acrylate monomer and an alkanolamine into a hydroxy-functional urethane prepolymer / monomer mixture and dispersing it in water.
• a radical initiator and a chain extender containing hydroxyl groups are then added to this dispersion and then, by heating the aqueous reaction mixture, both the radical polymerization of the acrylate monomers and the chain extension step of the polyurethane are carried out and completed.
• the hydroxy-functional polyurethane prepolymer / acrylic hybrid dispersions thus obtained can then be formulated into the ready-to-use two-component coating compositions by stirring in hydrophilized polyisocyanates.
• the disadvantage here is the use of up to 6% of molecular weight regulators, based on acrylate monomer, such as thiols, which can negatively influence important paint properties such as resistance properties and film hardness.
• the object of the present invention was therefore to provide a PUR-PAC hybrid dispersion in which polyisocyanates can be incorporated without problems and thus the production of high-quality coatings is possible.
• the coatings should have a very high gloss, generally greater than 80% residual gloss at a 20 ° angle, fullness and transparency and, at the same time, very good resistance properties, such as Resistance to water, solvents, chemicals, weather influences such as UV and weather resistance and mechanical stress e.g. Scratch resistance.
• the König pendulum hardness should reach values greater than 140 seconds.
• Such high quality clear and top coat systems are e.g. used in car serial painting, car refinishing, large vehicle painting, plastic or wood / furniture painting.
• the level of properties of the paint films can be significantly improved with regard to the requirements mentioned if the coating compositions contain aqueous polyurethane-polyacrylate hybrid secondary dispersions which are obtained by the fact that the Polymerization of the vinyl monomers in the presence of the polyurethane takes place in the non-aqueous phase, ie in bulk or before dispersion in an aqueous medium, without the need to use external emulsifiers or molecular weight regulators.
• the present invention thus relates to a process for the preparation of polyurethane-polyacrylate hybrid secondary dispersions, characterized in that
• step (A) added to the polyurethane solution from step (A) and radically polymerized in a homogeneous, non-aqueous phase,
• the hybrid polymer is then dispersed in the aqueous phase, the neutralization being able to take place before or after the vinyl polymerization or during the dispersing step.
• the invention also relates to polyurethane-polyacrylate hybrid selindar dispersions obtainable by the process according to the invention.
• the polyurethane (A) used to build up the PU-PAC hybrid secondary dispersions according to the invention can be built up from the building blocks which are fundamentally known in paint chemistry.
• (AI) polyisocyanates and at least one compound which contains groups reactive toward NCO groups and is selected from the group of
• (A3) compounds which have at least one ionic or potentially ionic group and at least one further group reactive toward isocyanate groups and / or compounds which have a nonionic hydrophilicity and have at least one further group reactive toward isocyanate groups,
• Polyisocyanates suitable as component (AI) are e.g. Diisocyanates of the molecular weight range 140 to 400 with aliphatic, cycloaliphatic, araliphatic and / or aromatically bound isocyanate groups, such as e.g.
• IPDI Isophorone diisocyanate
• 4'-diisocyanatodicyclohexylmethane 1-isocyanato-l-methyl-4 (3) isocyanatomethylcyclohexane, bis (isocyanatomethyl) norbornane, 1,3- and 1,4-bis (2-isocya - nato-prop-2-yl) -benzene (TMXDI), 2,4- and 2,6-diisocyanatotoluene (TDI), 2,4'- and 4,4'-diisocyanatodiphenylmethane, 1,5-diisocyanatonaphthalene or any mixtures of such diisocyanates.
• TXDI 2,4- and 2,6-diisocyanatototoluene
• TDI 2,4'- and 4,4'-diisocyanatodiphenylmethane
• polyisocyanates or polyisocyanate mixtures of the type mentioned with exclusively aliphatic and / or cycloaliphatic isocyanate groups.
• Particularly preferred starting components (AI) are polyisocyanates or polyisocyanate mixtures based on HDI, IPDI and / or 4,4'-diisocyanatodicyclohexylmethane.
• AI polyisocyanates
• any polyisocyanates made from at least two diisocyanates and containing uretdione, isocyanurate, urethane and polyisocyanates, which are prepared by modifying simple aliphatic, cycloaliphatic, araliphatic and / or aromatic diisocyanates. Allophanate, biuret, iminooxadiazinedione and / or oxadiazintiion structure, as described, for example, in J. Prakt. Chem. 336 (1994), pp. 185-200.
• Suitable compounds which contain groups reactive toward NCO groups are polyols and or polyamines (A2) which have an average molecular weight M "of 400 to 6000, preferably 600 to 2500.
• Their OH number and or NH number is generally 22 to 400, preferably 50 to 200 and their OH and / or NH functionality is greater than or equal to 1.6, preferably 2 to 4.
• polyols examples include polyether polyols, Polyester polyols, polycarbonate polyols, polyester carbonate polyols, polyester amide polyols, polyamide polyols, epoxy resin polyols and their reaction products with CO 2 , poly (meth) acrylate polyols, polyacetal polyols, saturated and unsaturated, optionally fluorinated hydrocarbon polyols and polysiloxane polyols.
• the polyether, polyester and polycarbonate polyols are preferred, and those which have only terminal OH groups and have a functionality of greater than or equal to 1.6, preferably from 2 to 4, are particularly preferred.
• the compounds of component ⁇ (A2) can also contain part or all of primary or secondary amino groups as NCO-reactive groups.
• Suitable polyether polyols are the polytetra methylene glycol polyethers known per se in polyurethane chemistry, which e.g. can be prepared via polymerization of tetrahydrofuran by cationic ring opening.
• Suitable polyether polyols are e.g. the polyols made from ethylene oxide, styrene oxide, propylene oxide, butylene oxide or epichlorohydrin, and copolymers of the cyclic monomers mentioned, prepared using starter molecules.
• polyester polyols The known polycondensates of di- and optionally poly (tri, tetra) ols and di- and optionally poly (tri, tetra) carboxylic acids or hydroxycarboxylic acids or lactones are suitable as polyester polyols.
• the corresponding polycarboxylic anhydrides or corresponding polycarboxylic acid esters of lower alcohols can also be used to prepare the polyesters.
• diols examples include ethylene glycol, butylene glycol, diethylene glycol, triethylene glycol, polyalkylene glycols such as polyethylene glycol, furthermore propanediol, butanediol (1,4), hexanediol (1,6), neopentyl glycol or hydroxypivalic acid neopentyl glycol ester.
• polyols such as trimethylolpropane, glycerol, erythritol, pentaerythritol, trimethylolbenzene or trishydroxyethyl isocyanurate can also be used.
• dicarboxylic acids examples include phthalic acid, isophthalic acid, terephthalic acid, tetrahydrophthalic acid, hexahydrophthalic acid, cyclohexanedicarboxylic acid, adipic acid, azelaic acid, sebacic acid, glutaric acid, tetrachlorophthalic acid, maleic acid, fumaric acid, itaconic acid, methyl acid, malonic acid, malonic acid, malonic acid, malonic acid, malonic acid, malonic acid, malonic acid, 2,2-dimethylsuccinic acid in question.
• the possible anhydrides of these acids are also suitable.
• the anhydrides are therefore encompassed by the term "acid".
• Monocarboxylic acids such as benzoic acid, hexane carboxylic acid or fatty acids can also be used, provided that the average functionality of the polyol is greater than 2.
• Saturated aliphatic or aromatic acids are preferred, such as adipic acid or isophthalic acid.
• Polycarboxylic acids such as trimellitic acid can be used in smaller amounts.
• Hydroxycarboxylic acids which can be used as real participants in the production of a polyester polyol having a terminal hydroxyl group are, for example, hydroxycaproic acid, hydroxybutyric acid, hydroxydecanoic acid or hydroxystearic acid.
• Suitable lactones are, for example, ⁇ -caprolactone or butyrolactone.
• the polycarbonates in question containing hydroxyl groups can be obtained by reaction of carbonic acid derivatives, e.g. Diphenyl carbonate, dimethyl carbonate or phosgene with diols available.
• carbonic acid derivatives e.g. Diphenyl carbonate, dimethyl carbonate or phosgene
• diols e.g.
• Ethylene glycol 1,2- and 1,3-propanediol, 1,3- and 1,4-butanediol, 1,6-hexanediol, 1,8-octanediol, neopentylglycol, 1,4-bishydroxymethylcyclohexane, 2-methyl-l, 3-propanediol, 2,2,4-trimethylpentanediol-1,3, dipropylene glycol, polypropylene glycols, dibutylene glycol, polybutylene glycols, bisphenol A, tetrabromobisphenol A but also lactone-modified diols in question.
• the diol component preferably contains 40 to 100% by weight of hexanediol, preferably 1,6-hexanediol and or hexanediol derivatives, particularly preferably those which have ether or ester groups in addition to terminal OH groups.
• the hydroxyl polycarbonates are preferably linear. However, if necessary, they can easily be branched by incorporating polyfunctional components, in particular low molecular weight polyols.
• Glycerol trimethylolpropane, hexanetriol-1,2,6, butanetriol-1,2,4, trimethylolpropane, pentaerythritol, quinite, mannitol and sorbitol, methylglycoside or 1,3,4,6-dianhydrohexite are suitable for this purpose.
• Component (A3) serves to hydrophilize the polyurethane.
• the dispersibility of the PUR-PAC hybrid polymer can take place both via the polyurethane and via the polyacrylate.
• Ionic or potentially ionic compounds suitable as component (A3) are, for example, mono- and dihydroxycarboxylic acids, mono- and diaminocarboxylic acids, mono- and dihydroxysulfonic acids, mono- and diaminosulfonic acids as well as mono- and dihydroxyphosphonic acids or mono- and diaminophosphonic acids and their salts such as dihydroxycarboxylic acids , Hydroxypivalic acid, N- (2-aminoethyl) -ß-alanine, 2- (2-aminoethylamino) ethanesulfonic acid, ethylenediamine propyl- or butylsulfonic acid, 1,2- or 1,3-propylenediamine-ß-ethylsulfonic acid, lysine, 3,5-di
• Preferred ionic or potentially ionic compounds (A3) are those which have carboxy or carboxylate and / or sulfonate groups.
• Particularly preferred ionic compounds (A3) are dihydroxycarboxylic acids, very particularly preferably ⁇ , ⁇ -dimethylolalkanoic acids, such as 2,2-dimethylolacetic acid, 2,2-dimethylolpropionic acid, 2,2-dimethylolbutyric acid, 2,2-dimethylolpentanoic acid or dihydroxy succinic acid.
• non-ionically hydrophilizing compounds e.g. Polyoxyalkylene ethers with at least one hydroxy or amino group can be used. These polyethers contain from 30% by weight to 100% by weight of building blocks which are derived from ethylene oxide. Linear polyethers with a functionality between 1 and 3 are suitable, but also compounds of the general formula (I)
• R 1 and R 2 each independently represent a divalent aliphatic, cycloaliphatic or aromatic radical with 1 to 18 C atoms, which can be interrupted by oxygen and / or nitrogen atoms, and
• R 3 represents a non-hydroxy-terminated polyester or preferably polyether, particularly preferably an alkoxy-terminated polyethylene oxide radical.
• the low molecular weight NCO-reactive compounds (A4) to be used optionally to build up the polyurethane (A) generally stiffen the polymer chain. They generally have a molecular weight of about 62 to 400, preferably 62 to 200, and can contain aliphatic, alicyclic or aromatic groups. examples are
• Alkanediols and polyols such as ethanediol, 1,2- and 1,3-propanediol, 1,4- and 2,3-butanediol, 1,5-pentanediol, 1,3-dimethylpropanediol, 1,6-hexanediol, neopentyl glycol , Cyclohexanedimethanol, 2-methyl-1,3-propanediol, bisphenol A (2,2-bis (4-hydroxyphenyl) propane), hydrogenated bisphenol A (2,2-bis (4-hydroxycyclohexyl) propane), Trimethylolpropane, glycerin or pentaerythritol,
• ether diols such as diethylene diglycol, triethylene glycol or hydroquinone dihydroxyethyl ether
• Di- and polyamines such as ethylenediamine, 1,2- and 1,3-diaminopropane, 1,4-diaminobutane, 1, 6-diaminohexane, isophoronediamine, mixture of isomers of 2,2,4- and 2,4,4-trimethyl hexamethylene diamine, 2-methyl-pentamethylene diamine, diethylene triamine, 1,3- and 1,4-xylylenediamine, ⁇ , ⁇ , ⁇ ', ⁇ '-tetramethyl-l, 3- and -1,4-xylylenediamine and 4, 4-diaminodicyclohexylmethane.
• Hydrazine as diamines in the sense of the invention are also
• hydrazine hydrate and substituted hydrazines e.g. N-methylhydrazine, N, N'-dimethylhydrazine and their homologues and acid dihydrazides, e.g. Adipic acid dihydrazide, semicarbazidoalkylene hydrazides, e.g. ß-Semicarbazidopropionic acid hydrazide, Semicarbazidoalkylencarbazinester, such as e.g. 2-semicarbazidoethylcarbazine esters or aminosemicarbazide compounds, such as e.g. ß-Aminoethylsemicarbazidocarbonate.
• acid dihydrazides e.g. Adipic acid dihydrazide
• semicarbazidoalkylene hydrazides e.g. ß-Semicarbazidopropionic acid hydrazide
• the polyurethane component (A) can also contain building blocks (A5), which are located at the chain ends and complete these.
• these building blocks are derived from monofunctional compounds which are reactive with NCO groups, such as monoamines, preferably from mono-secondary amines or monoalcohols.
• Examples include methylamine, Ethylamine, propylamine, butylamine, octylamine, laurylamine, stearylamine, isononyloxypropylamine, dimethylamine, diethylamine, ⁇ dipropylamine, dibutylamine, N-methylaminopropylamine, diethyl (methyl) aminopropylamine, morpholine, piperidine or suitable substituted derivatives thereof, amide amines of diprimary amines and monocarboxylic acids, Monocetime of diprimeric amines, primary / tertiary amines such as N, N-dimethylaminopropylamine.
• Preferred for (A5) are those compounds which contain active hydrogen with different reactivity than NCO groups, such as compounds which, in addition to a primary amino group, also contain secondary amino groups or, in addition to an OH group, also COOH groups or in addition to an amino group (primary or secondary) also have OH groups, the latter being particularly preferred.
• Examples of these are primary / secondary amines, such as 3-amino-1-methylaminopropane, 3-amino-1-ethylammopropane, 3-amino-1-cyclohexylaminopropane, 3-amino-1-methylaminobutane, mono-hydroxycarboxylic acids, such as hydroxyacetic acid, lactic acid or Malic acid, furthermore alkanolamines such as N-aminoethylethanolamine, ethanolamine, 3-aminopropanol, neopentanolamine and particularly preferably diethanolamine. In this way, additional functional groups are introduced into the polymer end product.
• primary / secondary amines such as 3-amino-1-methylaminopropane, 3-amino-1-ethylammopropane, 3-amino-1-cyclohexylaminopropane, 3-amino-1-methylaminobutane, mono-hydroxycarboxylic acids, such as
• the polyurethane (A) can be prepared, for example, in such a way that an isocyanate-functional prepolymer is first prepared and an OH-functional compound is obtained in a second reaction step by reaction with compounds (A4) and / or (A5).
• the polyurethane resin (A) is preferably prepared in such a way that a polyurethane is first of all formed from the polyisocyanates according to (A1), the polyols according to (A2) and the low molecular weight polyols according to (A4) and optionally the compounds according to (A3).
• Prepolymer is produced which contains an average of at least 1.7, preferably 2 to 2.5 free isocyanate groups per molecule, this prepolymer then with compounds according to (A4) and / or (A5) in a non-aqueous system to form an NCO group free polyurethane resin (A) is implemented.
• the polyurethane (A) is preferably prepared in the presence of at least some of the free-radically polymerizable monomers (B) which do not carry any groups which are reactive toward isocyanate groups.
• production can also be carried out in such a way that the polyurethane resin (A) is formed directly by reacting components (AI) to (A5).
• Anionic groups which may be present in the polyurethane (A) can be neutralized at least in part with bases before or after the vinyl polymerization or else during the dispersing step with water.
• the reaction for the preparation of the polyurethane (A) is normally carried out at from 60 to 140 ° C., depending on the reactivity of the isocyanate used.
• Suitable catalysts can be used in the urethanization reaction. Examples are tert. Amines such as triethylamine, organotin compounds such as dibutyltin oxide, dibutyltin dilaurate or tin bis (2-ethylhexanoate) or other organometallic compounds.
• the urethanization reaction is preferably sungsmitteln in the presence of inert toward isocyanates solu- •, such as ethers, ketones, esters, or N-methylpyrrolidone performed.
• the amount of these solvents expediently does not exceed 25% by weight and is preferably in the range from 0 to 15% by weight, based in each case on the sum of polyurethane resin and solvent.
• the urethanization reaction can also be carried out in the presence of at least some of the vinyl monomers which later form the vinyl polymer component of the hybrid polymer according to the invention and which do not carry any isocyanate-reactive functional groups (under the chosen reaction conditions). With this variant, there is the option of dispensing with the use of the solvents listed above or of reducing their amount.
• the polymerization of the vinyl monomers then takes place in the presence of the polyurethane (A) and, if appropriate, in the presence of further organic cosolvents and / or auxiliary solvents, but before the polyurethane is converted into the aqueous phase.
• Radically polymerizable vinyl monomers are selected from at least one of the group containing
• (B3) further polymerizable monomers different from (B1) and (B2).
• the PUR-PAC hybrid polymer is internally hydrophilized. This hydrophilization can take place via the polyurethane (A), by using component (A3) and / or the polyacrylate part, by using component (B1).
• the polyacrylate part is preferably hydrophilized.
• Unsaturated, free-radically polymerizable compounds with carboxyl / carboxylate groups or sulfonic acid / sulfonate groups are suitable as component (B1).
• acid-functional monomers (B1) are, for example, acrylic acid, methacrylic acid, ⁇ -carboxyethyl acrylate, crotonic acid, fumaric acid, maleic acid (anhydride), itaconic acid, monoalkyl esters of dibasic acids / anhydrides such as, for example, maleic acid monoalkyl esters, and those in WO-A 00/39181 (P.
• Suitable hydroxy-functional monomers (B2) are e.g. Hydroxyethyl methacrylate, hydroxypropyl methacrylate, hydroxyethyl acrylate, hydroxypropyl acrylate, hydroxybutyl acrylate, hydroxybutyl methacrylate or hydroxy monomers containing alkylene oxide units, such as e.g.
• Suitable monomers (B3) are, for example, (meth) acrylic acid ester with up to C 18 hydrocarbon radicals in the alcohol part, for example methyl acrylate, ethyl acrylate, n-butyl acrylate, iso-butyl acrylate, tert-butyl acrylate, 2-ethylhexyl acrylate, methyl methacrylate, ethyl methacrylate, 2-butyl methacrylate Ethylhexyl methacrylate, hexyl acrylate, lauryl acrylate, monomers containing cyclic hydrocarbon radicals such as cyclohexyl (meth) acrylate, cyclohexyl (meth) acrylates substituted with alkyl groups on the ring, isobornyl (meth) acrylate or norbornyl (meth) acrylate, monomers containing aromatic groups such as styrene, vinyl toluene or ⁇ -Met
• Di- or higher functional (meth) acrylate monomers and / or vinyl monomers such as hexanediol di (meth) acrylate, ethylene glycol diacrylate can also be used in amounts of 0-5% by weight, preferably 0-2% by weight, based on the sum of the monomers (B1). to (B3) are used.
• Methyl methacrylate, n-butyl acrylate, n-butyl methacrylate, 2-ethylhexyl acrylate, isobornyl acrylate, isobornyl methacrylate or styrene are preferably used.
• Organic peroxides such as di-tert-butyl peroxide or tert-butyl peroxy-2-ethylhexanoate and azo compounds are suitable as initiators for the polymerization reaction.
• the amounts of initiator used depend on the desired molecular weight. For reasons of process reliability and easier handling, peroxide initiators can also be used as a solution in suitable organic solvents of the type described in more detail below. It is preferred that the polyurethane-polyacrylate hybrid polymer according to the invention contains hydroxyl groups both in the polyurethane portion (A) and in the polyacrylate portion (B).
• the aqueous hybrid dispersions according to the invention are prepared by polymerizing components (B1) to (B3) and the initiator component and, if appropriate, additional organic cosolvents in the presence of the solution or melt of polyurethane (A), the polyurethane-polyacrylate hybrid polymer being polymerized forms.
• the free-radical polymerization can be carried out in the organic phase by polymerization processes known per se in paint chemistry x. ⁇ become.
• the radical polymerization is preferably carried out in such a way that at the end the proportion of the acid-functional monomers in the monomer mixture is higher than at the beginning.
• This can be done in a multi-stage polymerization process, e.g. described in EP-A 0 947 557 (page 3 line 2 - page 4 line 15) or in EP-A 1 024 184 (page 2 line 53 - page 4 line 9), in which a comparatively hydrophobic monomer mixture which is poor or free of acid groups is metered in first and then a more hydrophilic monomer group containing acid groups is added at a later point in the polymerization.
• the copolymerization is generally carried out at 60 to 180 ° C., preferably at 80 to 160 ° C. in the presence of the polyurethane (A).
• further organic co- or auxiliary solvents can be added before, during or after the polymerization.
• Suitable co- or auxiliary solvents the solvents known in paint technology, preferred are those which are usually used as cosolvents in aqueous dispersions, such as e.g. Alcohols, ethers, alcohols containing ether groups, esters, ketones, N-methylpyrrolidone or non-polar hydrocarbons or mixtures thereof.
• the solvents are used in amounts such that their content in the finished dispersion is 0 to 20% by weight, preferably 0 to 10% by weight. If necessary, the solvents used can also be partially removed again by distillation if particularly low organic solvent contents are required.
• the weight average molecular weight M w of the polyurethane-polyacrylate hybrid polymers is generally between 1000 and 50,000 and preferably between 2000 and 30,000.
• the OH content of the 100% hybrid polymers is 1 to 10% by weight, preferably 2.5 to 8% by weight.
• Acid group content which is the sum of carboxyl / carboxylate and sulfonic acid / sulfonate forms groups, the 100% hybrid polymer is 10 to 90 mequ./lOO g, preferably 15 to 70 mequ./100 g.
• both the resin can be added to the water and water to the resin, or both components can be added to one another at the same time.
• Organic amines or water-soluble inorganic bases e.g. soluble metal hydroxides
• Suitable amines are N-methylmorpholine, triethylamine, diisopropylethylamine, dimethylethanolamine, dimethylisopropanolamine, methyldiethanolamine, diefethylethanolamine, butanolamine, morpholine, 2-aminomethyl-2-methylpropanol, N, N-dimethylaminoethyl acrylate or isophoronediamine. Ammonia can also be used.
• the neutralizing agent is added in amounts such that there is a degree of neutralization (i.e. the molar ratio of neutralizing agent to acid) of 40 to 150%, preferably 60 to 120%.
• the pH of the aqueous crosslinkable polyurethane-polyacrylate hybrid dispersions according to the invention is 6.0 to 11.0, preferably 6.5 to 9.0 and has a solids content of 20 to 70%, preferably 25 to 60% and very particularly preferably 30 up to 60%.
• the polyurethane-polyacrylate hybrid secondary dispersions according to the invention can be processed into aqueous coating compositions.
• Aqueous two-component (2K) coating compositions containing the binder dispersions according to the invention and at least one crosslinking agent are therefore also an object of the present invention.
• Two-component lacquers in the sense of the present invention are coating compositions in which the binder component and crosslinker component have to be stored in separate containers because of their high reactivity.
• the two components are mixed shortly before application and then generally react without additional activation.
• catalysts can also be used to accelerate the crosslinking reaction, or higher temperatures can be used.
• Suitable crosslinking agents are, for example, polyisocyanate crosslinking agents, amide and amine formaldehyde resins, phenol resins, aldehyde and ketone resins, such as, for example, phenol formaldehyde resins, resols, furan resins, urea resins, carbamic acid ester resins, triazine resins, melamine resins, benzoguyanamide resins, anane resins, cyanine resins, cyanine resins as described in "Lackkunstharze", H. Wagner, HF Sarx, Carl Hanser Verlag Kunststoff, 1971. Polyisocyanate crosslinkers are preferred.
• polyisocyanates with free isocyanate groups based on aliphatic, cycloaliphatic, araliphatic and / or aromatic isocyanates, preferably aliphatic or cycloaliphatic isocyanates, since a particularly high level of resistance of the paint film can be achieved in this way.
• These polyisocyanates generally have a viscosity of 10 to 3500 mPas at 23 ° C. If necessary, the polyisocyanates can be used in a mixture with small amounts of inert solvents in order to reduce the viscosity to a value within the range mentioned.
• Triisocyanatononan can also be used alone or in mixtures as a crosslinking component.
• the polyurethane-polyacrylate hybrid polymer described here is generally sufficiently hydrophilic so that the dispersibility of the crosslinking resins, insofar as they are not water-soluble or water-dispersible substances, is ensured.
• the aqueous two-component coating compositions may also contain other binders or dispersions, e.g. based on polyesters, polyurethanes, polyethers, polyepoxides or polyacrylates and, if appropriate, pigments and other auxiliaries and additives known in the coatings industry.
• the auxiliaries and additives such as Defoamers, thickeners, pigments, dispersing aids, catalysts, skin-preventing agents, anti-settling agents or emulsifiers can be added before, during or after the dispersing step of the hybrid polymer, preferably with or • after adding the crosslinking agent.
• aqueous 2-component coating compositions thus obtained, containing the polyurethane-polyacrylate hybrid secondary dispersions according to the invention, are suitable for all areas of application in which aqueous coating and coating systems with high demands on the durability of the films are used, for example coating of mineral building materials.
• Surfaces such as concrete or screed, painting and sealing wood and wood-based materials, coating metallic surfaces (metal coating), coating and painting asphalt or bituminous coverings, painting and sealing various plastic surfaces (plastic coating), glass, glass fibers, carbon fibers, woven and non-woven textiles , Leather, paper, hard fibers, straw and high-gloss lacquers. It is preferred to paint metallic surfaces and plastic surfaces.
• aqueous two-component coating compositions containing the polyurethane-polyacrylate hybrid secondary dispersions according to the invention are used for the production of primers, fillers, pigmented or transparent topcoats, clearcoats and high-gloss paints, as well as Layered lacquers that can be used in single and series applications, e.g. in the field of industrial painting, automotive initial and repair painting, and floor coating.
• the present application also relates to substrates coated with aqueous coating compositions comprising the polyurethane-polyacrylate hybrid secondary dispersions according to the invention.
• Viscosity measurements were carried out in a cone-plate viscometer according to DIN 53019 at a shear rate of 40 s "1 .
• Example 1 Production of a hybrid dispersion according to the invention
• Desmodur ® W (4,4'-cyclohexylmethane Düsocyanatodi-, Bayer AG, Leverkusen, DE) was added within 2 minutes with stirring, the reaction mixture is heated to 140 ° C and stirred for 2 h at 140 ° C.
• the polyurethane has an average molecular weight M n of 3940 g / mol.
• the polyurethane is dissolved by adding 46.7 g of propylene glycol n-butyl ether and stirred for a further 10 minutes.
• a solution of 95.3 g of hydroxyethyl methacrylate, 33.8 g of styrene and 34.1 g of 2-ethylhexyl acrylate is metered in over the course of 2 hours.
• a solution of 24.0 g of di-tert-butyl peroxide and 24.0 g of propylene glycol n-butyl ether is added dropwise within 3.5 h.
• a mixture of 38.8 g of hydroxypropyl methacrylate, 20.0 g of n-butyl acrylate and 14.0 g of acrylic acid is metered in directly within 1 h.
• the reaction mixture is stirred for a further 2 hours at 140 ° C., then cooled to 100 ° C., mixed with 15.6 g of dimethylethanolamine and homogenized for 10 minutes.
• the dispersion is carried out by adding 529.3 g of water within 5 minutes.
• the hybrid resin has an average molecular weight M w of 14295 g / mol.
• Example 2 Preparation of a hybrid dispersion according to the invention
• Desmodur ® W (4,4'-Diisocyana- todicyclohexylmethan, Bayer AG, Leverkusen, DE) are added within 2 minutes with stirring, the reaction mixture is heated to 140 ° C and stirred for 2 h at 140 ° C.
• the polyurethane has an average molecular weight M n of 3940 g / mol.
• the polyurethane is dissolved by adding 46.7 g of propylene glycol n-butyl ether and stirred for a further 10 minutes.
• a solution of 105.2 g of hydroxypropyl acrylate, 41.2 g of styrene and 16.8 g of 2-ethylhexyl acrylate is added within 2 hours added.
• a solution of 24.0 g of di-tert-butyl peroxide and 24.0 g of propylene glycol n-butyl ether is added dropwise within 3.5 h.
• a mixture of 38.8 g of hydroxypropyl methacrylate, 19.6 g of n-butyl acrylate, 8.6 g of styrene and 5.0 g of acrylic acid is metered in directly within 1 h.
• the reaction mixture is stirred for a further 2 hours at 140 ° C., then cooled to 100 ° C., mixed with 6.5 g of dimethylethanolamine and homogenized for 10 minutes.
• the dispersion is carried out by adding 529.3 g of water within 5 minutes.
• the hybrid resin has an average molecular weight M w of 21382 g / mol.
• Example 3 Comparative Example from EP-A 742 239 (Example 1, page 7)
• example 1 of EP-A 742 239 described on page 7, line 19 ff. was reproduced.
• the hybrid resin thus obtained has an average molecular weight M w of 14556 g / mol; the dispersion had a solids content of 42.0%, an average particle size of 67.0 nm and a pH of 8.44.
• Example 4 Comparative example from EP 742239 (Example 1-1, page 15)
• Example 1-1 of EP-A 742 239 described on page 15 was reproduced as a comparative example.
• the average molecular weight M w of the hybrid resin thus obtained can no longer be measured by GPC. It should therefore have an average molecular weight M w of over 500,000 g / mol.
• Example 5 Comparative Example from EP-A 657 483 (Example 1, page 9)
• Example 6-10 Application engineering examples, formulation of an aqueous 2-component clear coat
• Bayhydur ® VPLS 2319 hydrophilized, cycloaliphatic isocyanurate group-containing polyisocyanate, Bayer AG, Leverkusen, DE. It is used in Examples 6-10 as an 80% solution in methoxybutyl acetate,
• Surfynol ® 104 BC flow additive, defoamer, Air Products, Utrecht, NL
• Baysüone ® VP AI 3468 slip additive, Borchers AG, Monheim, DE
• Tinuvin ® 1130 UV absorber, Ciba specialties GmbH, Lampertheim, DE
• Tinuvin ® 292 HALS-Amine, Ciba-Spezialitaten GmbH, Lampertheim, DE
• Desmodur ® N 3600 aliphatic polyisocyanate based on hexamethylene diisocyanate, Bayer AG, Leverkusen, DE
• Aqueous 2K clearcoats are formulated from the dispersions of Examples 1-5 in accordance with the recipes in Table 1.
• the polyisocyanate is incorporated using a Dispermat for 2 minutes at 2000 rpm.
• the water-based paints obtained in this way are then adjusted to a processing viscosity between 20 "and 25" (measured in a DFN 4 beaker at 23 ° C.) by adding water.
• the water-based varnishes are sprayed onto a coated with a Wasserbasecoat (Permahyd ®, Fa. Spies Hecker, Cologne, DE) sheet (dry film thickness 40-60 micrometers), air-dried 30 min at room temperature and baked for 30 minutes at 60 ° C.
• Table 1 Application examples using the dispersions from the
• Example 11 Preparation of a hybrid dispersion according to the invention
• a 41 reaction vessel with a cooling, heating and stirring are in a nitrogen atmosphere 186 g of a linear adipic acid / hexanediol poly 'ester diol g having a number average molecular weight of 2250, together with 186 of a linear Polyestercarbonatdiols the number average molecular weight of 2000 (Desmophen ® VP LS 2391, Bayer AG, Leverkusen, DE), 36 g 1,4-butanediol and 0.6 g tin (II) octoate heated to 80 ° C. and homogenized for 30 min.
• a linear adipic acid / hexanediol poly 'ester diol g having a number average molecular weight of 2250
• 186 of a linear Polyestercarbonatdiols the number average molecular weight of 2000 (Desmophen ® VP LS 2391, Bayer AG, Leverkus
• Desmodur ® W (4,4'-Diisocyanatodicyclohexylmefhan, Bayer AG, Leverkusen, DE) were added with vigorous stirring (using the exothermic nature of the reaction) to 140 ° C is heated and kept the mixture at this temperature, until no more NCO groups can be identified.
• the polyurethane has an average molecular weight M n of 5100 g / mol.
• the polyurethane obtained in this way is diluted by adding 204.7 g of propylene glycol n-butyl ether and then, at 140 ° to 143 ° C. in a nitrogen atmosphere, first a hydrophobic monomer mixture Ml, consisting of 394.5 g of hydroxypropyl methacrylate, 87 g n-butyl acrylate, 90 g styrene and 91.5 g methyl methacrylate, in 2 hours and immediately afterwards a hydrophilic monomer mixture M2, consisting of 145.5 g hydroxypropyl methacrylate, 75 g n-butyl acrylate and 52.5 g acrylic acid, in 1 hour and in parallel an initiator solution consisting of 39 g of di-t-butyl peroxide dissolved in 60 g of propylene glycol n-butyl ether is metered into these two monomer batches in 3.5 h (ie with a 30 min replenishment time of the initiator solution).
• Example 12 Preparation of a hybrid dispersion according to the invention
• the polyester resin thus obtained has a viscosity (determined as the outflow time of a 70% strength solution of the polyester in methoxypropylacetate in a DIN 4 beaker at 23 ° C.) of 100 seconds and an OH number of 53 mg KOH / g.
• the polyurethane obtained in this way is diluted by adding 174.7 g of propylene glycol n-butyl ether and then at 140 ° to 143 ° C. in a nitrogen atmosphere in succession first a hydrophobic monomer mixture Ml, consisting of 394.5 g of hydroxypropyl methacrylate, 76.5 g n-butyl acrylate, 75 g styrene and 66 g methyl methacrylate, in 2 hours and immediately afterwards a hydrophilic monomer mixture M2, consisting of 145.5 g hydroxypropyl methacrylate, 75 g n-butyl acrylate and 52.5 g acrylic acid, in 1 hour and in parallel
• An initiator solution consisting of 90 g of di-t-butyl peroxide dissolved in 90 g of propylene glycol n-butyl ether was metered into these two monomer batches in 3.5 h (ie with a 30 min replenishment time of the initiator solution).
• Example 13 Comparative example, not according to the invention
• Example 14 Clear coats for the first car painting
• the dispersions from Examples 11-13 are formulated into aqueous master lacquers in accordance with the weights in Table 2.
• the polyisocyanate hardener is incorporated by means of nozzle jet dispersion at a dispersion pressure of 50 bar.
• the water-based paints thus obtained are sprayed onto a metal sheet coated with a solvent-based standard basecoat (dry film thickness 30-40 ⁇ m), flashed off at room temperature for 5 minutes, then baked at 80 ° C. and 30 minutes at 130 ° C.
• the paint test results are summarized in Table 2.
• hybrid dispersions according to the invention (Ex. 11, 12) have advantages over the physical mixture of polyacrylate and polyurethane dispersion (Ex. 13) in aqueous 2-component PUR clearcoats with comparable film optics in solvent and chemical resistance as well as scratch resistance exhibit.
• Example 15 Preparation of a hybrid dispersion according to the invention
• the mixture is then cooled to 80 ° C., 120 g of hexamethylene diisocyanate are added with vigorous stirring, the mixture is heated to 140 ° C. (using the exotherm of the reaction) and the mixture is kept at this temperature until there are no more NCO groups have it determined.
• the polyurethane has an average molecular weight M n of 3620 g / mol.
• the polyurethane obtained in this way is then diluted by adding 204.7 g of propylene glycol n-butyl ether and then at 140 ° to 143 ° C. in a nitrogen atmosphere in succession first a hydrophobic monomer mixture Ml, consisting of 333 g of hydroxypropyl methacrylate, 87 g of n-butyl acrylate and 150 g of isobornyl methacrylate, in 2 hours and immediately afterwards a hydrophilic monomer mixture M2, consisting of 82.5 g hydroxypropyl methacrylate, 30 g n-butyl acrylate and 37.5 g acrylic acid, in 1 hour and in parallel with these two batches of monomer, an initiator solution consisting of 30 g of di-t-butyl peroxide dissolved in 60 g of propylene glycol n-butyl ether in 3.5 h (ie with a 30 min replenishment time of the initiator solution).
• the mixture is then stirred for a further 2 hours at the polymerization temperature, cooled to 90 ° to 100 ° C., 36 g of dimethylethanolamine (degree of neutralization 70%) are added, the mixture is homogenized for about 15 minutes and then with 1385 g of demin. Water dispersed.
• the hybrid resin thus obtained has an average.
• Talc IT Extra (Norway Tale, Frankfurt, DE), 35.3 parts by weight Bayferrox ® 318 M (Bayer AG, Leverkusen, DE), 4.4 parts by weight. Matting agent OK 412 (Degussa, Frankfurt, DE) and 65.6 parts by weight. demin. Water rubbed into an aqueous base lacquer component. Then 55.2 parts by weight are dissolver. a 75% solution of the polyisocyanate crosslinker Bayhydur ® 3100 (Bayer AG, Leverkusen, DE) in methoxypropylacetate.
• the varnish thus obtained is applied to a plastic plate (for example, Bayblend ® T 65, Bayer AG, Leverkusen, DE) spray applied (dry film thickness 40 micron 50 microns) and min after 10th Flash-off time 30 min at 80 ° C and then 16 h at 60 ° C. A matt, even lacquer film is obtained that feels velvety soft ("soft feel" feel). Adhesion to the substrate is good.
• the film has a good level of condensation water (DIN 50017) as well as resistance to premium petrol, methoxypropyl acetate, xylene, ethyl acetate, ethanol or water.
• Example 16 Preparation of a hybrid dispersion according to the invention
• the polyurethane obtained in this way is then diluted by adding 204.7 g of propylene glycol n-butyl ether and then, at 140 ° -143 ° C. in a nitrogen atmosphere, successively first of all a hydrophobic monomer mixture Ml, consisting of 120 g of hydroxypropyl methacrylate, 120 g of n-butyl acrylate and 120 g of isobornyl methacrylate and 15 g of acrylic acid, in 3 hours and in parallel an initiator solution, consisting of 15 g of di-t-butyl peroxide dissolved in 60 g of propylene glycol n-butyl ether in 3.5 h (ie with 30 min replenishment time of the initiator solution) , Then there will be stirred for a further 2 hours at the polymerization temperature, cooled to 90 ° to 100 ° C, 34 g of dimethylethanolamine (degree of neutralization 80%) added, the mixture was homogenized for about 15 minutes and then dem
• Talc IT Extra (Norway Tale, Frankfurt, DE), 23.0 parts by weight Bayferrox ® 318 M (Bayer AG, Lev., DE), 2.9 parts by weight. Matting agent OK 412 (Degussa, Frankfurt, DE) and 44.9 parts by weight. demin. Water rubbed into an aqueous base lacquer component. Then 23.2 parts by weight are dissolver. of a 75% solution of the polyisocyanate crosslinking agent Bayhydur 3100 ® (Bayer AG, Leverkusen, DE) incorporated in methoxypropyl acetate.
• the varnish thus obtained is applied to a plastic plate (for example, Bayblend ® T 65, Bayer AG, Leverkusen, DE) spritzappli formulate (dry film thickness about 30 microns) and min after 10th Flash-off time 30 min at 80 ° C and then 16 h at 60 ° C. A matt, even lacquer film is obtained, which feels velvety soft ("soft feel" feel). Adhesion to the substrate is very good. When exposed to solvents such as super gasoline, methoxypropyl acetate, xylene, ethyl acetate, ethanol or water, the film has a good level of resistance; The particularly good resistance in the condensation test (according to D1N 50017) should also be emphasized.
• a plastic plate for example, Bayblend ® T 65, Bayer AG, Leverkusen, DE
• spritzappli dry film thickness about 30 microns
• 10th Flash-off time 30 min at 80 ° C and then 16 h at 60 ° C.

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