Non-ionic hydrophilic polyurethane dispersions containing methacrylate double bonds

Abstract

The present invention relates to an aqueous UV-curable dispersion comprising at least a reaction product of a) at least one polyisocyanate having an average isocyanate functionality of at least 2.2, of which at least one polyisocyanate is preferably an oligomeric polyisocyanate having urethane, biuret, allophanate, iminooxadiazinedione and / or isocyanurate structural units, b) at least one monohydroxy-functional compound containing methacryloyl groups, c) at least one component containing non-ionic hydrophilic groups and having at least one further isocyanate-reactive group, and d) at least one diol, triol, diamine and / or triamine, the reaction product having neither ionogenic nor ionic hydrophilic groups. The present invention also relates to a method for its preparation, the use of the dispersion for the preparation of a glass fiber sizing agent, a glass fiber sizing agent containing at least said type of dispersion, glass fibers provided with a sizing agent obtained using said type of dispersion, a method for the preparation of glass fiber reinforced plastics, and the corresponding glass fiber reinforced plastics.

Description

[Technical field]

[0001] The present invention relates to an aqueous UV-curable dispersion comprising at least a reaction product formed from a) at least one polyisocyanate having an average isocyanate functionality of at least 2.2, of which at least one polyisocyanate is preferably an oligomeric polyisocyanate having urethane, biuret, allophanate, iminooxadiazinedione and / or isocyanurate structural units, b) at least one monohydroxy-functional compound containing methacryloyl groups, c) at least one component containing non-ionic hydrophilizing groups and having at least one isocyanate-reactive group, and d) at least one diol, triol, diamine and / or triamine, wherein the reaction product has neither ionogenic nor ionic hydrophilizing groups, a method for the preparation thereof, the use of the dispersion for the preparation of a glass fiber sizing, a glass fiber sizing comprising at least one dispersion of this kind, glass fibers with a sizing obtainable with a dispersion of this kind, a method for the preparation of glass fiber reinforced plastics, and the corresponding glass fiber reinforced plastics. [Background technology]

[0002] Aqueous coating agents based on functionalized polyisocyanates are known per se to the person skilled in the art. They are, for example, combined into one-component coating agents and used for coating glass fibers, for example glass fiber reinforced plastics. After application to the glass fibers, the water is first removed. The resulting film, the so-called sizing, is crosslinked by reaction of the potentially present polyisocyanates. Further crosslinking by reaction of the polyisocyanates present in the sizing then occurs when the glass fibers are incorporated into the plastic.

[0003] EP 1 516 012 B1 discloses a fiberglass sizing composition comprising at least one water-dispersible or water-soluble blocked polyisocyanate (A), at least one polyurethane (B) containing groups polymerizable by free radicals, and an initiator (C) capable of initiating free radical polymerization.

[0004] DE 10 2009 008 949 A1 describes radiation-curable coating systems based on aqueous polyurethane dispersions which contain as structural components one or more oligomeric or polymeric compounds having at least one isocyanate-reactive group and at least one group copolymerizable by free radicals, optionally one or more monomeric compounds having hydroxy functional groups and at least one (meth)acrylate group, polyester polyols, optionally further polyols, one or more compounds which have at least one isocyanate-reactive group and additionally ionic groups or groups which can form ionic groups or a combination of non-ionic and ionic groups or groups which can form ionic groups and which have a dispersing effect in the polyurethane dispersion, and organic polyisocyanates.

[0005] Acrylate- or methacrylate-functional coating agents known from the prior art show compatibility that can improve typical formulations for glass fiber sizing, which results, for example, in a significant reduction in processing time. The problem with the use of functional silanes in glass fiber sizing is that in typical glass fiber sizing, complex hydrolysis and condensation processes of other components in combination with the functional silanes often result in (intermediate) products that result in unstable systems. Highly compatible coating agents for glass fibers with (reactive) methacrylate groups have not been described in the prior art. [Prior art documents] [Patent documents]

[0006] [Patent Document 1] European Patent No. 1516012 [Patent Document 2] DE 102009008949 Summary of the Invention

[0007] It was therefore an object of the present invention to provide purely nonionically hydrophilized, functionalized polyisocyanates containing methacrylate groups, in particular for use as glass fiber sizing, and a process for their preparation. It is a further object of the present invention to provide aqueous dispersions of the corresponding polyisocyanates which have a sufficiently high storage stability.

[0008] According to the invention, these objectives are achieved by: a) at least one polyisocyanate having an average isocyanate functionality of at least 2.2, at least one of which is preferably an oligomeric polyisocyanate having urethane, biuret, allophanate, iminooxadiazinedione and / or isocyanurate structural units; b) at least one monohydroxy-functional compound containing a methacryloyl group; c) at least one component containing non-ionic hydrophilizing groups and having at least one isocyanate-reactive group; d) at least one diol, triol, diamine and / or triamine, preferably having a molecular weight of <400 g / mol wherein the reaction product has no ionogenic or ionic hydrophilizing groups.

[0009] Thus, the dispersions of the present invention comprise functionalized polyisocyanates that contain methacrylate groups polymerizable by high-energy radiation or by the addition of free-radical initiators, such as peroxide or azo-based curing agents, and that no longer contain free isocyanate groups.

[0010] The reaction products present in the UV curable dispersions of the present invention comprise the following components: 35% to 75% by weight, particularly preferably 40% to 75% by weight and very particularly preferably 45% to 65% by weight of component a), 10% to 50% by weight, particularly preferably 12% to 35% by weight and very particularly preferably 14% to 32% by weight of component b), 5% to 40% by weight, particularly preferably 7% to 30% by weight and very particularly preferably 15% to 25% by weight of component c), and 0.1% to 25% by weight, particularly preferably 0.1% to 9% by weight, very particularly preferably 0.1% to 5% by weight of component d) (wherein the percentages a) to d) in each case add up to 100% by weight) is obtained or is obtainable from the reaction of

[0011] The dispersions of the present invention may contain auxiliaries and additives, for example auxiliaries and additives that allow or promote curing by high-energy radiation, such as electron beam or UV radiation, or by free radical reactions. In a preferred embodiment, the dispersions contain stabilizers against premature curing from the group comprising phenols, sterically hindered amines and / or thiazines.

[0012] The dispersion of the present invention generally has an acid value of less than 50 mg KOH / g polymer, preferably less than 20 mg KOH / g polymer, particularly preferably less than 10 mg KOH / g polymer, and particularly preferably less than 5 mg KOH / g polymer.The acid value indicates the mass (mg) of potassium hydroxide required to neutralize 1 g of the sample to be examined (measurement according to DIN EN ISO 660 (2009 edition)).Neutralized acids, i.e. the corresponding salts, naturally have zero or reduced acid values.What is important here in the present invention is the acid value of the corresponding free acid.

[0013] The dispersions according to the invention generally have a zeta potential of -50 to +50 mV, preferably -15 to +15 mV, particularly preferably -2 to +10 mV. The zeta potential is determined by measuring a sample diluted in demineralized water in a "ZetaSizer 3000HSA" (Malvern Instruments, Herrenberg, Germany) at 23°C.

[0014] The urethane group content (MW urethane groups=59 g / mol) of the dispersions according to the invention is generally from 3% to 30% by weight, preferably from 10% to 25% by weight, in each case based on the solids content.

[0015] As well as oligomeric polyisocyanates which preferably have urethane, biuret, allophanate, iminooxadiazinedione and / or isocyanurate structural units, polyisocyanates a) suitable for the present invention are at least difunctional polyisocyanates, such as cyclohexane 1,4-, 1,3- and / or 1,2-diisocyanate, 1-methyl-2,4-diisocyanatocyclohexane, 1-methyl-2,6-diisocyanatocyclohexane, tetramethylene diisocyanate, octyl 2-methyl-2,4-diisocyanatocyclohexane, octyl 2-methyl-2,6-diisocyanatocyclohexane ... Tamethylene diisocyanate, decamethylene diisocyanate, dodecamethylene diisocyanate, H6-2,4- and / or H6-2,6-diisocyanatotoluene, 4,4'-diisocyanatodiphenylmethane, 2,4'-diisocyanatodiphenylmethane, 2,2'-diisocyanatodiphenylmethane, meta- and / or para-xylylene diisocyanate, 2,4-diisocyanatotoluene and / or 2,6-diisocyanatotoluene, isopropenyl dimethyl tolylene diisocyanate , α,α,α,'α,'-tetramethyl-m- and / or α,α,α,'α,'-tetramethyl-p-xylylene diisocyanate, hexamethylene 1,6-diisocyanate, trimethylhexane diisocyanate, tetramethylhexane diisocyanate, nonane triisocyanate, 1-isocyanato-3,3,5-trimethyl-5-isocyanatomethylcyclohexane (isophorone diisocyanate), 4,4'-diisocyanatodicyclohexylmethane and / or 2,4'-diisocyanato dicyclohexylmethane and / or 2,2'-diisocyanatodicyclohexylmethane, and mixtures of these diisocyanatodicyclohexylmethanes and their mono- and dimethyl-substituted derivatives and / or higher functional reaction products, homologues, oligomers and / or polymers of said at least difunctional polyisocyanates having urethane, biuret, carbodiimide, isocyanurate, allophanate, iminooxadiazinedione and / or uretdione structural units.It is also possible to use a proportion of monofunctional isocyanates such as stearyl isocyanate, butyl isocyanate, phenyl isocyanate, or other isocyanates such as 3-isocyanatopropyltrialkoxysilane.

[0016] The average isocyanate functionality of the polyisocyanate component a) is preferably 2.2 to 6, particularly preferably 2.4 to 5, very particularly preferably 2.6 to 4.5.

[0017] The polyisocyanate component a) preferably has a viscosity of less than 25 000 mPa·s at 23°C, particularly preferably less than 15 000 mPa·s at 23°C.

[0018] The polyisocyanate component a) is preferably composed of, to the extent of at least 40% by weight, liquid oligomeric polyisocyanates based on hexamethylene diisocyanate having isocyanurate, biuret, uretdione, carbodiimide, allophanate and / or iminooxadiazinedione structural units, and, to the extent of up to 60% by weight, isophorone diisocyanate, H6-2,4- or H6-2,6-trilidene diisocyanate, hexamethylene It consists of 1,6-diisocyanatodicyclohexylmethane and / or 2,4'-diisocyanatodicyclohexylmethane and / or 2,2'-diisocyanatodicyclohexylmethane and / or 2,4- or 2,6-trilidene diisocyanate or their reaction products with trimethylolpropane, butanediol, ethylene glycol, diethylene glycol, propylene glycol or neopentyl glycol.

[0019] Polyisocyanate component a) particularly preferably consists of oligomeric polyisocyanates based on hexamethylene diisocyanate to an extent of at least 70% by weight and having biuret, iminooxadiazinedione, allophanate and / or isocyanurate structural units, and to an extent of up to 30% by weight of isophorone diisocyanate, 4,4'-diisocyanatodicyclohexylmethane and / or 2,4'-diisocyanatodicyclohexylmethane and / or 2,2'-diisocyanatodicyclohexylmethane and / or 2,4- or 2,6-trilidene diisocyanate.

[0020] Suitable as component b) are compounds which have a monohydroxy-functional methacryloyl group, such as, for example, hydroxyethyl methacrylate, 2- / 3-hydroxypropyl methacrylate, hydroxybutyl methacrylate, 2- / 3- / 4-hydroxyethyl methacrylate, 2- / 3-hydroxypropyl methacrylate, 2- / 3- / 4-hydroxybutyl methacrylate, ethoxylation and / or propoxylation products of said hydroxymethacrylates, reaction products of trimethylolpropane, glycerol and / or pentaerythritol or their ethoxylation and / or propoxylation products with 2 or 3 equivalents of methacrylic acid, reaction products of said hydroxymethacrylates with caprolactone, reaction products of monoepoxides, such as Cardura® E10 (monoepoxide, Hexion Specialty Chemicals, The Netherlands), with methacrylic acid and mixtures of said compounds which have a monohydroxy-functional methacryloyl group.

[0021] According to the invention, preference is given to using hydroxyethyl methacrylate, hydroxypropyl methacrylate and / or hydroxybutyl methacrylate as component b).

[0022] The dispersion of the invention further comprises at least one component c) which contains non-ionic hydrophilizing groups and has at least one further isocyanate-reactive group. Component c) present according to the invention preferably has one or two, preferably one, isocyanate-reactive group and a non-ionic hydrophilizing structural unit, preferably based on a polyalkylene oxide.

[0023] Suitable as non-ionic hydrophilizing components c) are, for example, polyoxyalkylene ethers containing at least one hydroxy or amino group. These polyethers contain units derived from ethylene oxide in a proportion of 30% to 100% by weight. Useful compounds include polyethers of linear structure with a functionality of 1 to 3, but also compounds of general formula (I):

[0024] [ka]

[0025] [During the ceremony, R 1 and R 2 are each independently a divalent aliphatic, alicyclic or aromatic group having 1 to 18 carbon atoms, optionally interrupted by oxygen and / or nitrogen atoms, and R 3 is an alkoxy-terminated polyethylene oxide group. Non-ionic hydrophilizing compounds are also, for example, monohydric polyalkylene oxide polyether alcohols having a statistical average of 5 to 70 ethylene oxide units per molecule, as may be obtained in a manner known per se by alkoxylation of suitable starter molecules (see, for example, Ullmanns Encyclopaedie der technischen Chemie [Ullmann's Encyclopedia of Industrial Chemistry], 4th edition, Vol. 19, Verlag Chemie, Weinheim, pp. 31-38).

[0026] Examples of suitable starter molecules are saturated monoalcohols, such as methanol, ethanol, n-propanol, isopropanol, n-butanol, isobutanol, sec-butanol, the isomeric pentanols, hexanols, octanols and nonanols, n-decanol, n-dodecanol, n-tetradecanol, n-hexadecanol, n-octadecanol, cyclohexanol, the isomeric methylcyclohexanols or hydroxymethylcyclohexanes, 3-ethyl-3-hydroxymethyloxetane or tetrahydrofurfuryl alcohol, diethylene glycol monoalkyl ethers, such as diethylene glycol monobutyl ether, unsaturated aryl alcohols, such as ... Alcohols such as allyl alcohol, 1,1-dimethylallyl alcohol or oleic alcohol, aromatic alcohols such as phenol, the isomeric cresols or methoxyphenols, aromatic aliphatic alcohols such as benzyl alcohol, anisyl alcohol or cinnamyl alcohol, secondary monoamines such as dimethylamine, diethylamine, dipropylamine, diisopropylamine, dibutylamine, bis(2-ethylhexyl)amine, N-methyl- and N-ethylcyclohexylamine or dicyclohexylamine, and heterocyclic secondary amines such as morpholine, pyrrolidine, piperidine or 1H-pyrazole. Preferred starter molecules are saturated monoalcohols. Particular preference is given to using diethylene glycol monomethyl, monoethyl or monobutyl ether as starter molecule.

[0027] Suitable alkylene oxides for the alkoxylation reaction are in particular ethylene oxide and propylene oxide, which can be used in any order or in mixtures in the alkoxylation reaction.

[0028] The polyalkylene oxide polyether alcohols are either pure polyethylene oxide polyethers or mixed polyalkylene oxide polyethers, the alkylene oxide units being composed of ethylene oxide units to the extent of at least 30 mol %, preferably to the extent of at least 50 mol %.

[0029] Particularly preferred non-ionic compounds c) are monohydroxy-functional polyalkylene oxide polyethers which contain at least 75 mol % ethylene oxide units, particularly preferably 100 mol % ethylene oxide units and have number average molecular weights in the range from 350 to 2500 g / mol, particularly preferably in the range from 500 to 1100 g / mol, determined by gel permeation chromatography (GPC) according to DIN EN ISO 13885-2:2021 in DMAc (N,N-dimethylacetamide) as eluent at 23° C., by calibration with polystyrene standards.

[0030] The reaction products present in the dispersions of the invention have neither ionogenic groups, i.e. potentially ionic groups, nor ionic hydrophilizing groups. Preferably, the reaction products present in the dispersions of the invention have neither ionogenic groups, nor ionic hydrophilizing groups, nor the following compounds: Particularly preferably, the reaction products present in the dispersions of the invention have neither ionic hydrophilizing groups, i.e. the following units are preferably not used in the reactions a) to d): Mono- and dihydroxycarboxylic acids, mono- and diaminocarboxylic acids, mono- and dihydroxysulfonic acids, mono- and diaminosulfonic acids and mono- and dihydroxyphosphonic acids or mono- and diaminophosphonic acids and their salts, such as dimethylolpropionic acid, dimethylolbutyric acid, hydroxypivalic acid, N-(2-aminoethyl)alanine, 2-(2-aminoethylamino)ethanesulfonic acid, ethylenediaminepropyl- or -butylsulfonic acid, propylene-1,2- or propylene-1,3-diamineethylsulfonic acid, malic acid, citric acid, glycolic acid, lactic acid, glycine, alanine, taurine, lysine, 3,5-diaminobenzoic acid, IPDI and acrylic acid (EP-A 0 916 647, Example 1) and their alkali metal and / or ammonium salts; the adduct of sodium hydrogen sulfite onto 2-butene-1,4-diol, polyethersulfonates, propoxylated adducts of 2-butenediol and NaHSO3, for example those described in DE-A 2 446 440 (pages 5-9, formulae I-III), N-methyldiethanolamine, compounds having carboxy or carboxylate and / or sulfonate and / or ammonium groups, in particular compounds which contain carboxyl and / or sulfonate groups as ionic or potentially ionic groups, for example salts of 2-(2-aminoethylamino)ethanesulfonic acid, or addition products of diamines such as ethylenediamine or isophoronediamine and acrylic acid (EP-A 0 916 647, Example 1), or addition products of dimethylolpropionic acid.

[0031] In the context of the present invention, "no ionogenic or ionic hydrophilizing groups" generally means that, based on the reaction products present in the dispersion of the present invention, at least less than 100 milliequivalents per 100 g of polyurethane polymer are present, preferably less than 25 milliequivalents, particularly preferably less than 1 milliequivalent and very particularly preferably less than 1 milliequivalent per 100 g of polymer.

[0032] Component d) is a diol, triol, diamine and / or triamine, the purpose of which is to extend the chain or increase the molecular weight. The chain extension reaction between amino and isocyanate groups leads to the formation of urea structural units in the polyurethane polyacrylate dispersion. Optionally, it is also possible to use a certain proportion of hydroxylamine or monoamines with only one amino group, which then act as chain terminators.

[0033] Examples of component d) are ethylenediamine, propylene-1,3-diamine, hexamethylene-1,6-diamine, butane-1,4-diamine, hydrazine (hydrate), amino-functional polyethylene oxides or polypropylene oxides, which are available, for example, under the name Jeffamine® (from Huntsman Corp. Europe, Belgium), mono- or diamines containing alkoxysilane groups, diethylenetriamine, monoamines such as butylamine or diethylamine, triethylenetetramine, isophoronediamine, and hydroxyamines such as diethanolamine, hydroxyethylethylenediamine, and bishydroxyethylethylenediamine.Preference is given to linear aliphatic diamines such as ethylenediamine, hydrazine (hydrate) or hexamethylene-1,6-diamine and optionally aliphatic triamines such as diethylenetriamine.

[0034] When component d) is used according to the invention, it is used in an amount such that the degree of chain extension is from 30 to 200%, preferably from 50 to 150%, particularly preferably from 70 to 110%.

[0035] The degree of chain extension is defined as the ratio of the equivalents of amino groups in component d) to the equivalents of isocyanate groups in prepolymer A) obtained by reacting components a), b) and c). A degree of chain extension of 100% according to this definition is obtained when the amount of equivalents of amino groups in component d) corresponds exactly to the amount of equivalents of isocyanate groups in prepolymer A).

[0036] Examples of diols and triols which can be used are low molecular weight alcohols, such as butanediol, hexanediol, neopentyl glycol, diethylene glycol, triethylene glycol, propylene glycol, dipropylene glycol, tetraethylene glycol and / or trimethylolpropane, ethoxylated and / or propoxylated diols and / or triols, such as those based on diethylene glycol or trimethylolpropane, polycarbonate diols having a number average molecular weight in the range of 700 to 2200 g / mol, polycarbonate diols having a number average molecular weight in the range of 400 to 2000 g / mol Polyether diols, polyester diols, alkyd resins containing unsaturated fatty acids, and / or oligomers containing unsaturated groups, and / or hydroxy-functional and / or isocyanate-non-reactive liquid polymers, such as epoxy (meth)acrylates, ester (meth)acrylates, polyester (meth)acrylates, ether (meth)acrylates, polyether (meth)acrylates and / or urethane (meth)acrylates, having a number average molecular weight Mn in the range of 400 to 2000. Partial or complete incorporation into the polymer via hydroxyl groups is possible. The number average molecular weights are / were determined according to DIN EN ISO 13885-2:2021, respectively, by gel permeation chromatography (GPC) in DMAc (N,N-dimethylacetamide) as eluent at 23 °C after calibration with polystyrene standards.

[0037] The oligoesters are obtained by esterification of carboxylic acids, such as adipic acid, isophthalic acid, phthalic anhydride, maleic anhydride, fumaric acid, tetrahydrophthalic acid, hexahydrophthalic acid, dimer fatty acids, soybean oil fatty acids, benzoic acid and / or glutaric acid, with alcohols, such as neopentyl glycol, hexanediol, ethylene glycol, propylene glycol, butanediol, diethylene glycol, dipropylene glycol, cyclohexane-1,4-dimethanol, cyclohexane-1,4-diol, TCD diol, trimethylolpropane, glycerol and / or pentaerythritol. It is preferred to use adipic acid, isophthalic acid, phthalic anhydride, tetrahydrophthalic anhydride and / or hexahydrophthalic anhydride with neopentyl glycol, ethylene glycol, diethylene glycol, glycerol and / or trimethylolpropane. Particular preference is given to using isophthalic acid and phthalic anhydride, optionally in combination with adipic acid and neopentyl glycol, optionally in combination with trimethylolpropane.

[0038] In a preferred embodiment, low molecular weight diols, such as butanediol, hexanediol, neopentyl glycol, ethylene glycol, propylene glycol and / or polymeric diols, such as polycarbonate diols or polyester diols, or epoxy acrylates, ester acrylates and / or polyester acrylates, are used as component d).

[0039] In a further preferred embodiment, oligoesters are used as component d) having a hydroxyl number (OH number) of 240 to 500 mg KOH / g (determined according to DIN EN ISO 4629-2:2016), preferably 300 to 500 mg KOH / g substance, and a number average molecular weight Mw in the range of 200 to 400 g / mol, preferably in the range of 250 to 390 g / mol. The number average molecular weight is / was determined according to DIN EN ISO 13885-2:2021 by gel permeation chromatography (GPC) in DMAc (N,N-dimethylacetamide) as eluent at 23 ° C, respectively, after calibration with polystyrene standards.

[0040] In a preferred embodiment, component d) is selected from the group consisting of butanediol, hexanediol, neopentyl glycol, ethylene glycol, propylene glycol, ethylenediamine, isophoronediamine, hydrazine (hydrate), hexamethylene-1,6-diamine, diethylenetriamine and / or polymeric diols, in particular polycarbonate diols, polyester diols, epoxy acrylates, ester acrylates and polyester acrylates, where the polymeric diols are ... Preferably, the component d) has a number average molecular weight in the range of 700 to 2200 g / mol, determined in accordance with 13885-2:2021, and component d) is particularly preferably selected from the group consisting of butanediol, hexanediol, neopentyl glycol, ethylene glycol, propylene glycol, ethylenediamine, isophoronediamine, hydrazine (hydrate), hexamethylene-1,6-diamine and / or diethylenetriamine.

[0041] The dispersions of the invention can also be used as mixtures with other aqueous dispersions, which may also contain unsaturated groups, for example dispersions containing unsaturated, polymerizable groups based on polyesters, polyurethanes, polyepoxides, polyethers, polyamides, polysiloxanes, polycarbonates, polymers and / or polyacrylates.

[0042] It is also possible to mix dispersions based, for example, on polyesters, polyurethanes, polyepoxides, polyethers, polyamides, polyvinyl esters, polyvinyl ethers, polysiloxanes, polycarbonates, polymers or polyacrylates and containing functional groups such as alkoxysilane, hydroxy or isocyanate groups. For example, dual cure systems can be produced which are curable via two different mechanisms.

[0043] The present invention also provides coating agents comprising the UV-curable polyisocyanate-based dispersions of the present invention and crosslinkers based on amino resins and / or polyisocyanates and / or blocked polyisocyanates.

[0044] Suitable amino crosslinking resins are, for example, those based on melamine or urea.Suitable polyisocyanates are, for example, those mentioned under description a).Hydrophilic agents suitable in principle for polyisocyanates, for example those based on polyethers, are mentioned under description c).Examples of suitable blocking agents are methanol, ethanol, butanol, hexanol, benzyl alcohol, acetoxime, butanone oxime, caprolactam, phenol, diethyl malonate, diethyl malonate, dimethylpyrazole, triazole, dimethyltriazole, ethyl acetoacetate, diisopropylamine, dibutylamine, tert-butylbenzylamine, ethyl cyclopentanone carboxylate, dicyclohexylamine and / or tert-butylisopropylamine.

[0045] It is also possible to mix dispersions based on polyesters, polyurethanes, polyepoxides, polyethers, polyamides, polysiloxanes, polyvinyl ethers, polybutadienes, polyisoprenes, chlorinated rubbers, polycarbonates, polyvinyl esters, polyvinyl chlorides, polymers or polyacrylates which do not have functional groups.

[0046] Also suitable for combination with the dispersions of the present invention may be what are known as reactive diluents, low-viscosity compounds having unsaturated groups, such as hexanediol bisacrylate, trimethylolpropane trisacrylate, trimethylolpropane diacrylate, pentaerythritol tetraacrylate, dipentaerythritol hexaacrylate or bisphenol A-based diepoxide bisacrylate. The present invention also provides a binder combination comprising the UV-curable polyisocyanate-based dispersion of the present invention and one or more further dispersions.

[0047] The dispersions of the present invention can also be used as mixtures with water-insoluble or water-dispersible oligomers or polymers containing unsaturated groups, where the water-insoluble or water-dispersible oligomers or polymers containing unsaturated groups are added to the dispersions of the present invention before dispersion, whereby the dispersions of the present invention act as polymeric emulsifiers for these materials. A preferred mixture is a combination of the dispersions of the present invention and a binder comprising a water-insoluble or water-dispersible oligomer or polymer containing unsaturated groups.

[0048] The invention also provides a process for the preparation of the inventive dispersion, in which the isocyanate-functional prepolymer A) is obtained by reacting components b) and c) with an excess of component a) in one or more reaction steps, followed by a dispersion step by addition of water or transfer of the prepolymer A) to an aqueous receiver vessel to form the prepolymer A), followed by a chain extension step by addition of component d).

[0049] The invention also provides a method for the preparation of the inventive dispersion, wherein the isocyanate-functional prepolymer A) is obtained by reacting components a), b) and c) with an excess of component a) in one or more reaction steps, followed by a chain extension step by addition of component d), followed by a dispersion step by addition of water to form the prepolymer A) or by transfer of the prepolymer A) to an aqueous receiving vessel.

[0050] The dispersion of the present invention generally has a solid content (non-volatile content) of 25% by weight to 65% by weight, preferably 35% by weight to 60% by weight.

[0051] In the process of the invention, organic solvents and / or catalysts can be used for the preparation of the prepolymer A). Suitable catalysts for the preparation of the prepolymer A) or the dispersion of the invention are in principle all those which catalyze the reaction of hydroxyl groups with isocyanate groups, for example tertiary amines, tin compounds, zinc compounds, zirconium compounds, copper compounds and / or bismuth compounds, preferably triethylamine, ethyldiisopropylamine, dimethylcyclohexylamine, N-methylmorpholine, 1,4-diazabicyclo[2.2.2]octane, tin dioctoate or dibutyltin dilaurate. Salts of zinc, titanium and molybdenum are also suitable. Suitable amounts are, for example, 0.002% to 1% by weight, preferably 0.01% to 0.1% by weight. The reaction can also be carried out without the use of catalysts.

[0052] The dispersion of the present invention is generally produced at a temperature of 20 to 150°C, preferably 25 to 75°C.

[0053] In the process of the present invention, component d) may be present diluted with water and / or organic solvent.The solvent optionally used can then be removed by distillation.Although solvent-free preparation is possible, preparation in organic solvent is preferred.

[0054] The dispersions according to the invention generally contain less than 5% by weight, preferably less than 1% by weight, particularly preferably less than 0.5% by weight of organic solvent.

[0055] Production in 3% to 50% by weight of acetone (non-volatile fraction of the acetone solution), particularly preferably 5% to 25% by weight of acetone, followed by distillative removal of the solvent after production of the dispersion or during the dispersion process is preferred.

[0056] Suitable solvents are in principle all solvents or solvent mixtures that do not react with the reactants, such as N-butylpyrrolidone, butyl acetate, ethyl acetate, methoxypropyl acetate, diethylene glycol dimethyl ether, dioxane, dimethylformamide, xylene, toluene, solvent naphtha, cyclohexanone, methyl isobutyl ketone, diethyl ketone, methyl ethyl ketone, and acetone.Some of these solvents can then be completely or partially removed by distillation.After the dispersion of the present invention is produced, it is also possible to add further solvents, such as hydroxy-functional solvents, such as butyl diglycol, methoxypropanol, or butyl glycol.

[0057] The dispersions of the present invention can be used to make fiberglass sizing.

[0058] The present invention therefore also relates to the use of the dispersion of the present invention for producing a glass fiber sizing.

[0059] The present invention also relates to a fiberglass sizing comprising at least one dispersion according to the invention.

[0060] The present invention also relates to glass fibres provided with a sizing obtained using the dispersion of the present invention.

[0061] The glass fiber sizing generally comprises a dispersion of the present invention, optionally at least one binder, and optionally auxiliaries and additives.

[0062] To prepare the aqueous sizing composition, the components present are preferably mixed one after the other in any order or simultaneously.

[0063] Preferably, the aqueous fiberglass sizing of the present invention may optionally contain additional binders, such as polyurethane dispersions, polyacrylate dispersions, polyurethane-polyacrylate hybrid dispersions, polyvinyl ether or polyvinyl ester dispersions, polystyrene or polyacrylonitrile dispersions (including combinations with other blocked polyisocyanates and amino crosslinking resins, such as melamine resins). In a preferred embodiment, no other binders than the dispersion of the present invention are used.

[0064] The glass fiber sizing of the present invention may contain customary auxiliaries and additives, such as antifoaming agents, thickeners, leveling agents, dispersants, catalysts, antiskinning agents, antisettling agents, antioxidants, plasticizers, reactive diluents, emulsifiers, biocides, adhesion promoters, such as those based on known low or high molecular weight silanes, lubricants, wetting agents, antistatic agents.

[0065] The adhesion promoters used are, for example, known silane adhesion promoters, such as 3-aminopropyltrimethoxysilane or triethoxysilane, N-(2-aminoethyl)-3-aminopropyltrimethoxysilane, 3-glycidylpropyltrimethoxysilane, vinyltrimethoxysilane, vinyltriethoxysilane or 3-methacryloxypropyltriethoxysilane. The concentration of the silane adhesion promoter in the glass fiber sizing according to the invention is preferably 0.05% to 2% by weight, particularly preferably 0.15% to 0.85% by weight, in each case based on the entire sizing.

[0066] The fiberglass sizing of the invention can include one or more nonionic and / or ionic lubricants, which can be selected, for example, from the following groups of substances: polyalkylene glycol ethers of fatty alcohols or fatty amines, glycerol esters of polyalkylene glycol ethers and fatty acids having 12 to 18 carbon atoms, polyalkylene glycols, higher fatty acid amides having 12 to 18 carbon atoms of polyalkylene glycols and / or alkylene amines, quaternary nitrogen compounds, such as ethoxylated imidazolinium salts, mineral oils, and waxes. The one or more lubricants are preferably used in a total concentration of 0.05% to 1.5% by weight, based on the entire fiberglass sizing.

[0067] The fiberglass sizing of the present invention may include one or more antistatic agents, such as lithium chloride, ammonium chloride, Cr(III) salts, organotitanium compounds, aryl alkyl sulfates or sulfonates, aryl polyglycol ether sulfonates, or quaternary nitrogen compounds. The antistatic agents are preferably used at a concentration of 0.01% to 0.8% by weight, based on the total fiberglass sizing.

[0068] Furthermore, the glass fiber sizing of the present invention may further optionally comprise further auxiliaries and additives known from the prior art, for example as described in KL Loewenstein, "The Manufacturing Technology of Continuous Glass Fibres", Elsevier Scientific Publishing Corp., Amsterdam, London, New York, 1983.

[0069] The glass fiber sizing of the present invention can be prepared by methods known per se. For example, about half of the total water required, as well as the binder, hardener, are added to a suitable mixing vessel, followed by the addition of lubricants and other customary auxiliaries, if used, with stirring. The pH is then adjusted, preferably to 5-7, and an adhesion promoter hydrolysate, for example a trialkoxysilane hydrolysate, prepared according to the manufacturer's (e.g. UCC, New York) instructions, is added. After a further stirring time, for example 15 minutes, the sizing is ready for use, and the pH is further adjusted, if necessary, to 5-7.

[0070] The fiberglass sizing can be applied to the fiberglass by any desired method, for example, using suitable equipment such as a spray or roller applicator.

[0071] Suitable glass fibers are both the known types of glass used in glass fiber production, such as types E, A, C and S glass, as well as other products known per se from glass fiber manufacturers. Preferred are type E glass fibers, which are used to produce continuous glass fibers due to their absence of alkalis, high tensile strength and high modulus for the reinforcement of plastics.

[0072] Methods for manufacturing, sizing, and reprocessing glass fibers are known and are described, for example, in KL Loewenstein, "The Manufacturing Technology of Continuous Glass Fibres," Elsevier Scientific Publishing Corp., Amsterdam, London, New York, 1983.

[0073] Glass fiber sizing is usually applied to the glass filaments drawn at high speed from the spinneret immediately after solidification, i.e. before winding. However, it is also possible to size the fibers in an immersion bath after the spinning process. The sized glass fibers can be processed, for example, into chopped glass, which can be carried out either wet or dry. The proportion of sizing is preferably 0.1% to 5.0% by weight, particularly preferably 0.1% to 3.0% by weight, very particularly preferably 0.3% to 1.5% by weight, based on the sized glass fibers.

[0074] In one variant, the sized glass fibres are dried in several stages: first, the water and any solvents present are removed from the sizing by heat, convection, thermal radiation and / or dehumidified air. This is then followed by curing by UV irradiation. Irradiation devices of the prior art are used. High or medium pressure mercury lamps are preferred, which may optionally be doped with elements such as gallium or iron. It may also be useful to combine several irradiation devices one after the other, next to each other or in any desired three-dimensional arrangement. It may also be expedient to carry out the UV irradiation at elevated temperatures, between 30 and 200 ° C.

[0075] In another variant, the sized glass fibres undergo essentially physical drying: the water and any solvents present are removed from the sizing by heat, convection, thermal radiation and / or dehumidified air, so that the methacrylate groups present are largely unreacted at this stage and remain as methacrylate groups. This variant is preferred.

[0076] The sized glass fibers can then be incorporated into a matrix polymer. Many thermoplastic or thermosetting polymers can be used as the matrix polymer. Examples of suitable thermoplastic polymers are: polyolefins, such as polyethylene or polypropylene, polyvinyl chloride, polymers, such as styrene / acrylonitrile copolymers, ABS, polymethacrylates or polyoxymethylene, aromatic and / or aliphatic polyamides, such as polyamide 6 or polyamide 6,6, polycondensates, such as polycarbonates, polyethylene terephthalates, liquid crystal polyaryl esters, polyarylene oxides, polysulfones, polyarylene sulfides, polyarylsulfones, polyethersulfones, polyaryl ethers or polyether ketones or polyadditions, such as polyurethanes. Thermosetting polymers include, for example: epoxy resins, unsaturated polyester resins, vinyl resins, acrylate-functional resins, methacrylate-functional resins, phenolic resins, amine resins, polyurethane resins, polyisocyanurates, epoxy / isocyanurate combination resins, furan resins, cyanurate resins, and bismaleimide resins. The incorporation into the polymer matrix can be carried out according to the general conventional methods known to those skilled in the art (e.g. extrusion). In a preferred variant, the uncured matrix units contain groups with double bonds, such as allyl, vinyl, acrylate, olefin or methacrylate groups. They then undergo curing, preferably initiated, for example, by UV light, electron beam, heat, free radical initiators or a combination of the mentioned methods. The curing can be carried out according to the general methods known to those skilled in the art.

[0077] The present invention also relates to a method for producing a glass fiber reinforced plastic, comprising at least the following steps: (A) applying a glass fiber sizing of the present invention to glass fibers to obtain sized glass fibers; (B) introducing the sized glass fibers into a plastic matrix; and (C) chemically reacting, at least in part, the methacrylate groups of the glass fiber sizing with the groups of the plastic matrix, involving the formation of covalent bonds, to obtain a glass fiber reinforced plastic. The present invention relates to a method comprising the steps of:

[0078] Suitable plastics have already been mentioned above. The process parameters such as temperature, pressure, suitable equipment, etc. are known per se to the person skilled in the art.

[0079] The invention will now be illustrated by examples. EXAMPLES

[0080] Chemicals used: Desmodur® Ultra N 3300 isocyanurate based on hexamethylene diisocyanate, Covestro Deutschland AG, Leverkusen, DE Other chemicals were obtained from Sigma-Aldrich Chemie GmbH (Taufkirchen, Germany) unless otherwise stated.

[0081] Unless otherwise stated, all percentages are percent by weight (wt %).

[0082] Unless otherwise stated, all analytical measurements were performed at a temperature of 23°C.

[0083] The reported viscosities were determined by rotational viscosimetry at 23° C. according to DIN 53019-2008 using a rotational viscometer from Anton Paar Germany GmbH, Ostfildern, Germany.

[0084] The NCO content was determined volumetrically according to DIN-EN ISO 11909-2007, unless otherwise stated.

[0085] The reported particle sizes were determined by laser correlation spectroscopy (instrument: Malvern Zetasizer 1000, Malvern Inst. Limited) after dilution of the samples with demineralized water.

[0086] The solids content was determined by heating a weighed sample to 120° C. At constant weight, the solids content was calculated by reweighing the sample.

[0087] Free NCO groups were monitored by infrared spectroscopy (2260 cm -1 The performance was conducted by the band.

[0088] For storage testing, 250 ml of the dispersion was stored at room temperature, 40° C. Samples were visually monitored for the formation of a precipitate. Samples with a precipitate were deemed unstable.

[0089] All molecular weights or molar masses referred to in this application are defined by gel permeation chromatography (GPC) according to DIN EN ISO 13885-2:2021 in DMAc (N,N-dimethylacetamide) as eluent at 23° C., unless otherwise stated, calibrated using polystyrene standards.

[0090] The OH number (hydroxyl value) is determined / defined in accordance with DIN EN ISO 4629-2:2016.

[0091] Invention Example DSB9705-HEMA-functionalized crosslinker A standard stirring apparatus was charged with 1261 g of Desmodur Ultra N 3300, 0.9 g of tin(II) chloride, 0.05 g of phenothiazine, and 0.5 g of BHT in 240 g of acetone and heated to 50° C. Then, 660 g of 2-hydroxyethyl methacrylate was slowly added to the solution and the mixture was allowed to react in boiling acetone for 5 hours.

[0092] Then 470 g of methoxypolyethylene glycol having a number average molar mass of 750 g / mol and 26 g of butane-1,4-diol were added and the mixture was stirred at the boil until the isocyanate groups were no longer detectable by IR spectroscopy.

[0093] Then 2960 g of deionized water were added with vigorous stirring and the acetone was distilled off under reduced pressure at 40°C.

[0094] The resulting dispersion had the following properties: Solid content: approx. 44% by weight pH: approx. 3.5 Viscosity: Approximately 110mPa·s Average particle size (LCS): 124nm The dispersion was stable for at least 4 weeks of storage at room temperature and at 40° C. No phase separation occurred during this time.

[0095] Exemplary Formulations of Fiberglass Sizing To determine basic suitability in common fiberglass sizing, exemplary formulations were prepared according to the table below and stored at room temperature for 12 days.

[0096] Exemplary Formulations:

[0097] [Table 1]

[0098] Observations: No change in viscosity or phase separation was observed over 12 days at room temperature.

Claims

Claim 1 An aqueous UV-curable dispersion comprising: a) at least one polyisocyanate having an average isocyanate functionality of at least 2.2, at least one of which is preferably an oligomeric polyisocyanate having urethane, biuret, allophanate, iminooxadiazinedione and / or isocyanurate structural units, at least one polyisocyanate; b) at least one monohydroxy-functional compound containing a methacryloyl group; c) at least one component containing a nonionic hydrophilic group and having at least one isocyanate-reactive group; d) at least one diol, triol, diamine and / or triamine, preferably at least one diol, triol, diamine and / or triamine having a molecular weight of <400 g / mol; and at least comprising a reaction product formed therefrom, characterized in that the reaction product has neither an ionogenic group nor an ionic hydrophilic group. Claim 2 The reaction product is the following components: a) 35 wt% to 75 wt%, preferably 40 wt% to 75 wt%, more preferably 45 wt% to 65 wt% of component a); b) 10 wt% to 50 wt%, preferably 12 wt% to 35 wt%, more preferably 14 wt% to 32 wt% of component b); c) 5 wt% to 40 wt%, preferably 7 wt% to 30 wt%, more preferably 15 wt% to 25 wt% of component c), and d) 0.1 wt% to 25 wt%, preferably 0.1 wt% to 9 wt%, more preferably 0.1 wt% to 5 wt% of component d) (wherein the percentages from a) to d) are each 100 wt% in total in each case); The aqueous UV-curable dispersion according to claim 1, characterized in that it is obtained from the reaction of Claim 3 The polyisocyanate component a) is a hexamethylene diisocyanate-based oligomeric polyisocyanate having at least about 40% by weight of a liquid at room temperature and having isocyanurate, biuret, uretdione, carbodiimide and / or iminooxadiazinedione structural units, and up to about 60% by weight of isophorone diisocyanate, H ６ -2,4- or H ６ -2,6-tolylidene diisocyanate, hexamethylene 1,6-diisocyanate, 4,4'-diisocyanatodicyclohexylmethane and / or 2,4'-diisocyanatodicyclohexylmethane and / or 2,2'-diisocyanatodicyclohexylmethane and / or 2,4- or 2,6-tolylidene diisocyanate or reaction products thereof with trimethylolpropane, butanediol, ethylene glycol, diethylene glycol, propylene glycol or neopentyl glycol, characterized in that it consists of the aqueous UV-curable dispersion according to claim 1 or 2. Claim 4 The aqueous UV-curable dispersion according to claim 1 or 2, characterized in that the polyisocyanate component a) is based on hexamethylene diisocyanate to an extent of at least about 70% by weight and is an oligomeric polyisocyanate having biuret, iminooxadiazinedione and / or isocyanurate structural units, and isocyanophorone diisocyanate, 4,4'-diisocyanatodicyclohexylmethane and / or 2,4'-diisocyanatodicyclohexylmethane and / or 2,2'-diisocyanatodicyclohexylmethane and / or 2,4- or 2,6-tolylene diisocyanate to an extent of 30% by weight or less.

5. The aqueous UV-curable dispersion according to claim 1 or 2, characterized in that it contains 0.5% to 40% by weight of component e).

6. The aqueous UV-curable dispersion according to claim 1 or 2, characterized in that at least one monohydroxy-functional polyalkylene oxide polyether having a molecular weight of 500 to 1100 g / mol is used as component c).

7. The aqueous UV-curable dispersion according to claim 1 or 2, characterized in that component d) is used in an amount such that the chain extension degree is 100% to 200%.

8. The aqueous UV-curable dispersion according to claim 1 or 2, characterized in that it has an acid value (measured according to EN ISO 660 (2009 edition)) of less than 50 mg KOH / g polymer, preferably less than 20 mg KOH / g polymer, more preferably less than 10 mg KOH / g polymer, and even more preferably less than 5 mg KOH / g polymer.

9. Component d) is selected from the group consisting of butanediol, hexanediol, neopentyl glycol, ethylene glycol, propylene glycol, ethylenediamine, isophoronediamine, hydrazine (hydrate), hexamethylene-1,6-diamine, diethylenetriamine and / or polymer diol, in particular polycarbonate diol, polyester diol, epoxy acrylate, ester acrylate, and polyester acrylate, wherein the polymer diol preferably has a number average molecular weight in the range of 700 to 2200 g / mol as determined by gel permeation chromatography according to DIN EN ISO 13885-2:2021 at 23 °C in N,N-dimethylacetamide as eluent, calibrated using a polystyrene standard, and component d) is particularly preferably selected from the group consisting of butanediol, hexanediol, neopentyl glycol, ethylene glycol, propylene glycol, ethylenediamine, isophoronediamine, hydrazine (hydrate), hexamethylene-1,6-diamine and / or diethylenetriamine, an aqueous UV-curable dispersion according to claim 1 or 2, characterized in that.

10. The method for producing an aqueous UV-curable dispersion according to claim 1 or 2, characterized in that the isocyanate-functional prepolymer A) is obtained by reacting components a), b) and c) with an excess of component a) in one or more reaction steps, then performing a chain extension step by adding component d), and then performing a dispersion step by adding water to form prepolymer A) or transferring prepolymer A) to an aqueous receiver vessel.

11. The method for producing an aqueous UV-curable dispersion according to claim 1 or 2, characterized in that the isocyanate-functional prepolymer A) is obtained by reacting components b) and c) with an excess of component a) in one or more reaction steps, then performing a dispersion step by adding water to form prepolymer A) or transferring prepolymer A) to an aqueous receiver vessel, and then performing a chain extension step by adding component d).

12. Use of the aqueous UV-curable dispersion according to claim 1 or 2 for producing glass fiber sizing.

13. A glass fiber sizing containing at least the aqueous UV-curable dispersion according to claim 1 or 2.

14. Glass fibers provided with a sizing obtained using the aqueous UV-curable dispersion according to claim 1 or 2.

15. A method for producing a glass fiber-reinforced plastic, comprising at least the following steps: (A) Applying the glass fiber sizing according to claim 13 to glass fibers to obtain sized glass fibers; (B) Introducing the sized glass fibers into a plastic matrix; and (C) Chemically reacting at least partially the methacrylate groups of the glass fiber sizing with the groups of the plastic matrix to form covalent bonds to obtain a glass fiber-reinforced plastic. A method comprising the above steps.

16. A glass fiber-reinforced plastic comprising the glass fibers according to claim 14.

17. A glass fiber-reinforced plastic comprising glass fibers sized with the glass fiber sizing according to claim 13.