AU2011304536B2

AU2011304536B2 - Prepregs on the basis of a storage-stable reactive or highly reactive polyurethane composition

Info

Publication number: AU2011304536B2
Application number: AU2011304536A
Authority: AU
Inventors: Arnim Kraatz; Sandra Reemers; Friedrich Georg Schmidt
Original assignee: Evonik Degussa GmbH
Current assignee: Evonik Operations GmbH
Priority date: 2010-09-23
Filing date: 2011-08-30
Publication date: 2014-03-13
Anticipated expiration: 2031-08-30
Also published as: CA2811063A1; DE102010041239A1; MX2013003169A; KR20130109142A; RU2013118433A; ZA201302838B; EP2619256A1; AU2011304536A1; US20130231022A1; TW201226453A; BR112013006846A2; WO2012038200A1; CN103210023A; JP2013537928A

Abstract

The invention relates to prepregs, which are chromatically adjusted with pigment or dye preparations, on the basis of a storage-stable reactive or highly reactive polyurethane composition.

Description

Prepregs on the basis of a storage-stable reactive or highly reactive polyurethane composition The invention relates to prepregs coloured with pigment or dye preparations and based on storage-stable reactive or highly reactive polyurethane composition. Prepregs based on a storage-stable reactive or highly reactive polyurethane composition are known from DE 102009001793, DE 102009001806, DE 10201029355. It was an object of the present invention to enable the production of coloured prepregs based on a storage-stable reactive or highly reactive polyurethane composition. The stated object is achieved with pigment or dye preparations which are suitable for powder coating applications and are already present in the course of prepreg production in the matrix material composition based on storage-stable reactive or highly reactive polyurethane compositions. A subject of the invention are coloured prepregs, essentially made up of A) at least one fibrous support and B) at least one reactive or highly reactive polyurethane composition as matrix material, wherein the polyurethane compositions essentially contain mixtures of a polymer b) having functional groups reactive towards isocyanates as binder and di- or polyisocyanate internally blocked and/or blocked with blocking agents as curing agent a), wherein the matrix material additionally comprises 1. pigments having a particle diameter of < 150 nm and/or 2. dyes. In a first aspect, the present invention relates to prepregs, essentially made up of A) at least one fibrous support and B) with a matrix material of at least one polyurethane composition B) containing uretdione groups, essentially containing a) at least one uretdione group-containing curing agent, based on polyaddition compounds from aliphatic, (cyclo)aliphatic or cycloaliphatic uretdione group containing polyisocyanates and hydroxyl group-containing compounds, wherein the la curing agent is in solid form below 400C and in liquid form above 1250C, and has a free NCO content of less than 5 wt.% and a uretdione content of 3 - 25 wt.%, b) at least one hydroxyl group-containing polymer which is in solid form below 40*C and in liquid form above 125*C and has an OH number between 20 and 200 mg KOH/gram, c) optionally at least one catalyst, and d) optionally auxiliary agents and additives known from polyurethane chemistry, so that the two components a) and b) are present in the ratio such that for each hydroxyl group of the component b) 0.3 to 1 uretdione group of the component a) is consumed, preferably 0.45 to 0.55, and wherein the matrix material additionally comprises 1. pigments having a particle diameter of < 150 nm and/or 2. dyes. The production of the prepregs can in principle be effected by any process. In a suitable manner, a powdery polyurethane composition B) comprising the dyes and/or pigments is applied onto the support by powder impregnation, preferably by a dusting process. Also possible are fluidized bed sinter processes, pultrusion or spray processes. The powder (as WO 2012/038200 PCT/EP2011/064895 2 a whole or a fraction) is preferably applied by dusting processes onto the fibrous support, e.g. onto ribbons of glass, carbon or aramid fibre scrims/fabrics, and then fixed. For avoidance of powder losses, the powder-treated fibrous support is preferably heated in a heated section (e.g. with IR rays) directly after the dusting procedure, so that the particles are sintered on, during which temperatures of 80 to 100*C should not be exceeded, in order to prevent initiation of reaction of the highly reactive matrix material. These prepregs can as required be combined into different forms and cut to size. The production of the prepregs can also be effected by the direct melt impregnation process. The principle of the direct melt impregnation process for the prepregs consists in that firstly a reactive or highly reactive polyurethane composition B) comprising the dyes and/or pigments is produced from the individual components thereof in the melt. This melt of the reactive polyurethane composition B) comprising the dyes and/or pigments is then applied directly onto the fibrous support A), in other words an impregnation of the fibrous support A) with the melt from B) is effected. After this, the cooled storable prepregs can be further processed into composites at a later time. Through the direct melt impregnation process according to the invention, very good impregnation of the fibrous support takes place, due to the fact that the then liquid low viscosity reactive polyurethane compositions wet the fibres of the support very well. The production of the prepregs can also be effected using a solvent. The principle of the process for the production of prepregs then consists in that firstly a solution or dispersion the reactive or highly reactive polyurethane composition B) comprising dyes and/or pigments is produced from the individual components thereof in a suitable common solvent. This solution or dispersion of the reactive polyurethane composition B) is then applied directly onto the fibrous support A), whereby the fibrous support becomes soaked/impregnated with this solution. Next, the solvent is removed. Preferably the solvent is removed completely at low temperature, preferably < 100C, e.g. by heat treatment or application of a vacuum. After this, the storable prepregs again freed from the solvent can be further processed to composites at a later time. Through the process according to the invention, very good impregnation of the fibrous support takes place, due to the fact that the solutions of the reactive polyurethane compositions wet the fibres of the support very well.

WO 2012/038200 PCT/EP2011/064895 3 As suitable solvents for the process according to the invention, all aprotic liquids can be used which are not reactive towards the reactive polyurethane compositions, exhibit adequate solvent power towards the individual components of the reactive polyurethane composition used and can be removed from the prepreg impregnated with the reactive polyurethane composition during the solvent removal process step apart from slight traces (< 0.5 weight %), whereby recycling of the separated solvent is advantageous. By way of example, ketones (acetone, methyl ethyl ketone, methyl isobutyl ketone, cyclo hexanone), ethers (tetrahydrofuran), esters (n-propyl acetate, n-butyl acetate, isobutyl acetate, 1,2-propylene carbonate, propylene glycol methyl ether acetate) may be mentioned here. After cooling to room temperature, the prepregs according to the invention exhibit very high storage stability at room temperature, provided that the matrix material exhibits a Tg of at least 400C. Depending on the reactive polyurethane composition contained this is at least a few days at room temperature, but as a rule the prepregs are storage-stable for several weeks at 400C and below. The prepregs thus produced are not sticky and are thus very good for handling and further processing. The reactive or highly reactive polyurethane compositions used according to the invention thus exhibit very good adhesion and distribution on the fibrous support. During the further processing of the prepregs to composites (composite materials) e.g. by pressing at elevated temperatures, very good impregnation of the fibrous support takes place, due to the fact that the then liquid low viscosity reactive or highly reactive polyurethane compositions before the crosslinking reaction wet the fibres of the support very well, before gelling occurs or the complete polyurethane matrix cures fully due to the crosslinking reaction of the reactive or highly reactive polyurethane composition at elevated temperatures. The prepregs thus produced can as required be combined into different forms and cut to size. For the consolidation of the prepregs into a single composite and the crosslinking of the matrix material to give the matrix, the prepregs are cut to size, optionally sewn or otherwise fixed and compressed in a suitable mould under pressure and optionally application of vacuum. In the context of this invention, depending on the curing time this procedure of the production of the composites from the prepregs is effected at temperatures of over about 1600C with the use of WO 2012/038200 PCT/EP2011/064895 4 reactive matrix materials (modification 1) or at temperatures of over 100*C with highly reactive matrix materials provided with appropriate catalysts (modification 1l). Depending on the composition of the reactive or highly reactive polyurethane composition used and optionally added catalysts, both the rate of the crosslinking reaction in the production of the composite components and also the properties of the matrix can be varied over wide ranges. In the context of the invention, the reactive or highly reactive polyurethane composition used for the production of the prepregs is defined as the matrix material, and in the description of the prepregs the still reactive or highly reactive polyurethane composition applied onto the fibres by the process according to the invention. The matrix is defined as the matrix materials from the reactive or highly reactive polyurethane compositions crosslinked in the composite. Support The fibrous support in the present invention consists of fibrous material (also often called reinforcing fibres). In general, any material of which the fibres consist is suitable, however, fibrous material of glass, carbon, plastics such as for example polyamide (aramid) or polyester, natural fibres or mineral fibre materials such as basalt fibres or ceramic fibres (oxide fibres based on aluminium oxides and/or silicon oxides) is preferably used. Mixtures of fibre types, such as for example fabric combinations of aramid and glass fibres, or carbon and glass fibres, can be used. Likewise, hybrid composite components with prepregs of different fibrous supports can be produced. Mainly because of their relatively low price, glass fibres are the most commonly used fibre types. In principle here, all types of glass-based reinforcing fibres are suitable (E glass, S glass, R glass, M glass, C glass, ECR glass, D glass, AR glass, or hollow glass fibres). Carbon fibres are generally used in high performance composite materials, where the lower density in comparison to glass fibres with at the same time higher strength is also an important factor. Carbon fibres are industrially produced fibres made from carbon-containing starting materials which are converted by pyrolysis into carbon in graphite configuration. A distinction is made between isotropic and anisotropic: isotropic fibres have only low strength and lower industrial importance, anisotropic fibres exhibit high strength and rigidity with at the same time low WO 2012/038200 PCT/EP2011/064895 5 elongation at break. Here all textile fibres and fibre materials obtained from plant and animal material (e.g. wood, cellulose, cotton, hemp, jute, flax, sisal or bamboo fibres) are described as natural fibres. Similarly also to carbon fibres, aramid fibres exhibit a negative coefficient of thermal expansion, i.e. become shorter on heating. Their specific strength and modulus of elasticity are markedly lower than that of carbon fibres. In combination with the positive coefficient of expansion of the matrix resin, highly dimensionally stable components can be manufactured. Compared to carbon fibre-reinforced plastics, the compressive strength of aramid fibre composite materials is markedly lower. Well-known brand names for aramid fibres are Nomex@ and Kevlar@ from DuPont, or Teijinconex@, Twaron@ and Technora@ from Teijin. Supports made of glass fibres, carbon fibres, aramid fibres or ceramic fibres are particularly suitable and preferred. The fibrous material is a flat textile sheet. Flat textile sheets of non woven material, also so-called knitted goods, such as hosiery and knitted fabrics, but also non knitted sheets such as woven fabrics, non-wovens or braided fabrics, are suitable. In addition, a distinction is made between long-fibre and short-fibre materials as supports. Also suitable according to the invention are rovings and yarns. All the said materials are suitable as fibrous supports in the context of the invention. An overview of reinforcing fibres is contained in "Composites Technologies, Paolo Ermanni (Version 4), Script for Lecture at ETH Zorich, August 2007, Chapter 7". Matrix Material In principle, all reactive or highly reactive polyurethane compositions, even others which are storage-stable at room temperature, are suitable as matrix materials. According to the invention, suitable polyurethane compositions consist of mixtures of a polymer b) (binder) having functional groups - reactive towards NCO groups, also described as resin, and di- or polyisocyanates that are temporarily deactivated, in other words internally blocked and/or blocked with blocking agents, also described as curing agents a) (component a)). As functional groups of the polymers b) (binder), hydroxyl groups, amino groups and thiol groups which react with the free isocyanate groups with addition and thus crosslink and cure the polyurethane composition are suitable. The binder components must be of a solid resin nature (glass transition temperature greater than room temperature). Possible binders are polyesters, polyethers, polyacrylates, polycarbonates and polyurethanes with an OH number of 20 to 500 mg KOH/gram and an average molecular weight of 250 to 6000 g/mole. Particularly preferably hydroxyl group-containing polyesters or polyacrylates with an OH number of 20 to 150 mg WO 2012/038200 PCT/EP2011/064895 6 KOH/gram and an average molecular weight of 500 to 6000 g/mole are used. Of course, mixtures of such polymers can also be used. The quantity of the polymers b) having functional groups is selected such that for each functional group of the component b) 0.6 to 2 NCO equivalents or 0.3 to 1 uretdione group of the component a) is consumed. As the curing component a), di and polyisocyanates that are blocked with blocking agents or internally blocked (uretdione) are used. The di and polyisocyanates used according to the invention can consist of any aromatic, aliphatic, cycloaliphatic and/or (cyclo)aliphatic di and/or polyisocyanates. As aromatic di- or polyisocyanates, in principle, all known aromatic compounds are suitable. Particularly suitable are 1,3- and 1,4-phenylene diisocyanate, 1,5-naphthylene diisocyanate, tolidine diisocyanate, 2,6-toluylene diisocyanate, 2,4-toluylene diisocyanate (2,4-TDI), 2,4'-diphenylmethane diisocyanate (2,4'-MDI), 4,4'-diphenylmethane diisocyanate, the mixtures of monomeric diphenylmethane diisocyanates (MDI) and oligomeric diphenylmethane diisocyanates (polymeric MDI), xylylene diisocyanate, tetramethylxylylene diisocyanate and triisocyanatotoluene. Suitable aliphatic di- or polyisocyanates advantageously possess 3 to 16 carbon atoms, preferably 4 to 12 carbon atoms, in the linear or branched alkylene residue and suitable cycloaliphatic or (cyclo)aliphatic diisocyanates advantageously possess 4 to 18 carbon atoms, preferably 6 to 15 carbon atoms, in the cycloalkylene residue. (Cyclo)aliphatic diisocyanates are adequately understood by those skilled in the art simultaneously to mean cyclically and aliphatically bound NCO groups, as is for example the case with isophorone diisocyanate. In contrast, cycloaliphatic diisocyanates are understood to mean those which only have NCO groups directly bound to the cycloaliphatic ring, e.g. H 12 MDI. Examples are cyclohexane diisocyanate, methylcyclohexane diisocyanate, ethylcyclohexane diisocyanate, propylcyclohexane diisocyanate, methyldiethylcyclohexane diisocyanate, propane diisocyanate, butane diisocyanate, pentane diisocyanate, hexane diisocyanate, heptane diisocyanate, octane diisocyanate, nonane diisocyanate, nonane triisocyanate, such as 4-isocyanatomethyl-1,8 octane diisocyanate (TIN), decane di and triisocyanate, undecane di and triisocyanate, and dodecane di and triisocyanate.

WO 2012/038200 PCT/EP2011/064895 7 Isophorone diisocyanate (IPDI), hexamethylene diisocyanate (HDI), diisocyanatodicyclohexyl methane (HM 12 DI), 2-methylpentane diisocyanate (MPDI), 2,2,4-trimethylhexamethylene diisocyanate/2,4,4-trimethylhexamethylene diisocyanate (TMDI) and norbornane diisocyanate (NBDI) are preferred. Quite particularly preferably IPDI, HDI, TMDI and/or H 12 MDI are used, and the isocyanurates are also usable. Also suitable are 4-methyl-cyclohexane 1,3-diisocyanate, 2-butyl-2-ethylpentamethylene diisocyanate, 3(4)-isocyanatomethyl-1-methylcyclohexyl isocyanate, 2-isocyanatopropylcyclohexyl isocyanate, 2,4'-methylenebis(cyclohexyl) diisocyanate and 1,4-diisocyanato-4-methylpentane. Of course, mixtures of the di and polyisocyanates can also be used. Further, oligo or polyisocyanates which can be produced from the said di- or polyisocyanates or mixtures thereof by linking by means of urethane, allophanate, urea, biuret, uretdione, amine, isocyanurate, carbodiimide, uretonimine, oxadiazinetrione or iminooxadiazinedione structures are preferably used. Isocyanurate, in particular from IPDI and/or HDI, are particularly suitable. The polyisocyanates used according to the invention are blocked. Possible for this are external blocking agents, such as for example ethyl acetoacetate, diisopropylamine, methyl ethyl ketoxime, diethyl malonate, E-caprolactam, 1,2,4-triazole, phenol or substituted phenols and 3,5-dimethylpyrazole. The curing agents preferably used are IPDI adducts which contain isocyanurate groups and E-caprolactam-blocked isocyanate structures. Internal blocking is also possible and this is preferably used. The internal blocking occurs via dimer formation via uretdione structures which at elevated temperature cleave back again to the isocyanate structures originally present and hence set the crosslinking with the binder in motion. Optionally, the reactive polyurethane compositions can contain additional catalysts. These are organometallic catalysts, such as for example dibutyl tin dilaurate (DBTL), tin octoate, bismuth neodecanoate, or else tertiary amines, such as for example 1,4-diazabicyclo[2.2.2.]octane, in quantities of 0.001 - 1 wt.%. These reactive polyurethane compositions used according to the nvention are cured under normal conditions, e.g. with DBTL catalysis, beyond 1600C, usually beyond ca. 1800C and designated as modification I.

WO 2012/038200 PCT/EP2011/064895 8 For the production of the reactive polyurethane compositions, the additives usual in powder coating technology, such as levelling agents, e.g. polysilicones or acrylates, light stabilizers e.g. sterically hindered amines, or other additives, such as were for example described in EP 669 353, can be added in a total quantity of 0.05 to 5 wt.%. In the context of this invention, reactive (modification I) means that the reactive polyurethane compositions used according to the invention as described above cure at temperatures beyond 1600C, depending on the nature of the support. The reactive polyurethane compositions according to the invention are cured under normal conditions, e.g. with DBTL catalysis, beyond 160*C, usually beyond ca. 1800C. The time for the curing of the polyurethane composition used according to the invention as a rule lies within 5 to 60 minutes. Preferably in the present invention a matrix material B) is used made of a polyurethane composition B) containing uretdione groups, essentially containing a) at least one uretdione group-containing curing agent, based on polyaddition compounds from aliphatic, (cyclo)aliphatic or cycloaliphatic uretdione group-containing polyisocyanates and hydroxyl group-containing compounds, wherein the curing agent is in solid form below 400C and in liquid form above 1250C and has a free NCO content of less than 5 wt.% and a uretdione content of 3 - 25 wt.%, b) at least one hydroxyl group-containing polymer which is in solid form below 400C and in liquid form above 1250C and has an OH number between 20 and 200 mg KOH/gram, c) optionally at least one catalyst, and d) optionally auxiliary agents and additives known from polyurethane chemistry, so that the two components a) and b) are present in the ratio such that for each hydroxyl group of the component b) 0.3 to 1 uretdione group of the component a) is consumed, preferably 0.45 to 0.55. The latter corresponds to a NCO/OH ratio of 0.9 to 1.1 to 1.

WO 2012/038200 PCT/EP2011/064895 9 Uretdione group-containing polyisocyanates are well known and are for example described in US 4,476,054, US 4,912,210, US 4,929,724 and EP 417 603. A comprehensive overview concerning industrially relevant processes for the dimerization of isocyanates to uretdiones is given in J. Prakt. Chem. 336 (1994) 185-200. In general, the conversion of isocyanates to uretdiones takes place in the presence of soluble dimerization catalysts such as for example dialkylaminopyridines, trialkylphosphines, phosphorous acid triamides or imidazoles. The reaction - optionally performed in solvents, but preferably in the absence of solvents - is stopped by addition of catalyst poisons on attainment of a desired conversion level. Excess monomeric isocyanate is then removed by short path evaporation. If the catalyst is sufficiently volatile, the reaction mixture can be freed from the catalyst in the course of the monomer removal. In this case the addition of catalyst poisons can be omitted. Essentially, a broad range of isocyanates are suitable for the production of uretdione group-containing polyisocyanates. The aforesaid di and polyisocyanates can be used. However, di and polyisocyanates from any aliphatic, cyclo aliphatic and/or (cyclo)aliphatic di and/or polyisocyanates are preferable. According to the invention, isophorone diisocyanate (IPDI), hexamethylene diisocyanate (HDI), diisocyanato dicyclohexylmethane (H 1 2 MDI), 2-methylpentane diisocyanate (MPDI), 2,2,4-trimethyl hexamethylene diisocyanate/2,4,4-trimethylhexamethylene diisocyanate (TMDI) or norbornane diisocyanate (NBDI) are used. Quite particularly preferably, IPDI, HDI, TMDI and/or H 1 2 MDI are used, and the isocyanurates are also usable. Quite particularly preferably, IPDI and/or HDI are/is used for the matrix material. The conversion of these uretdione group-containing polyisocyanates to uretdione group-containing curing agents a) comprises the reaction of the free NCO groups with hydroxyl group-containing monomers or polymers, such as for example polyesters, polythioethers, polyethers, polycaprolactams, polyepoxides, polyester amides, polyurethanes or low molecular weight di, tri and/or tetrahydric alcohols as chain extenders and optionally monoamines and/or monohydric alcohols as chain terminators and has already often been described (EP 669 353, EP 669 354, DE 30 30 572, EP 639 598 or EP 803 524). Preferred curing agents a) having uretdione groups have a free NCO content of less than 5 wt.% and a content of uretdione groups of 3 to 25 wt.%, preferably 6 to 18 wt.% (calculated as

C

2

N

2 0 2 , molecular weight 84). Polyesters and monomeric dihydric alcohols are preferred. Apart from the uretdione groups, the curing agents can also have isocyanurate, biuret, allophanate, urethane and/or urea structures.

WO 2012/038200 PCT/EP2011/064895 10 For the hydroxyl group-containing polymers b), polyesters, polyethers, polyacrylates, polyurethanes and/or polycarbonates with an OH number of 20 - 200 in mg KOH/gram are preferably used. Polyesters with an OH number of 30 - 150 and an average molecular weight of 500 - 6000 g/mole which are in solid form below 400C and in liquid form above 125*C are particularly preferably used. Such binders have for example been described in EP 669 354 and EP 254 152. Of course, mixtures of such polymers can also be used. The quantity of the hydroxyl group-containing polymers b) is selected such that for each hydroxyl group of the component b) 0.3 to 1 uretdione group of the component a), preferably 0.45 to 0.55, is consumed. Optionally, additional catalysts c) can be contained in the reactive polyurethane compositions B) according to the invention. These are organometallic catalysts such as for example dibutyltin dilaurate, zinc octoate, bismuth neodecanoate, or else tertiary amines such as for example 1,4-diazabicyclo[2.2.2.]octane, in quantities of 0.001 - 1 wt.%. These reactive polyurethane compositions used according to the invention are cured under normal conditions, e.g. with DBTL catalysis, beyond 160*C, usually beyond ca. 1800C and designated as modification I. For the production of the reactive and highly reactive polyurethane compositions according to the invention, the additives usual in powder coating technology, e.g. polysilicones or acrylates, light stabilizers e.g. sterically hindered amines, or other additives, such as were for example described in EP 669 353, can be added in a total quantity of 0.05 to 5 wt.%. The reactive polyurethane compositions used according to the invention are cured under normal conditions, e.g. with DBTL catalysis, beyond 1600C, usually beyond ca. 1800C. The reactive polyurethane compositions used according to the invention provide very good flow and hence good impregnation behaviour and in the cured state excellent chemicals resistance. In addition, with the use of aliphatic crosslinking agents (e.g. IPDI or H 12 MDI) good weather resistance is also achieved. Particularly preferably in the invention a matrix material is used which is made from B) at least one highly reactive uretdione group-containing polyurethane composition, essentially containing a) at least one uretdione group-containing curing agent and b) optionally at least one polymer with functional groups reactive towards NCO groups; WO 2012/038200 PCT/EP2011/064895 11 c) 0.1 to 5 wt.% of at least one catalyst selected from quaternary ammonium salts and/or quaternary phosphonium salts with halogens, hydroxides, alcoholates or organic or inorganic acid anions as counter-ion; and d) 0.1 to 5 wt.% of at least one cocatalyst, selected from dl) at least one epoxide and/or d2) at least one metal acetylacetonate and/or quaternary ammonium acetylacetonate and/or quaternary phosphonium acetylacetonate; and e) optionally auxiliary agents and additives known from polyurethane chemistry. Quite especially, a matrix material B) made from B) at least one highly reactive powdery uretdione group-containing polyurethane composition as matrix material, essentially containing a) at least one uretdione group-containing curing agent, based on polyaddition compounds from aliphatic, (cyclo)aliphatic or cycloaliphatic uretdione group-containing polyisocyanates and hydroxyl group-containing compounds, wherein the curing agent is in solid form below 400C and in liquid form above 1250C and has a free NCO content of less than 5 wt.% and a uretdione content of 3 - 25 wt.%, b) at least one hydroxyl group-containing polymer which is in solid form below 400C and in liquid form above 125*C and has an OH number between 20 and 200 mg KOH/gram; c) 0.1 to 5 wt.% of at least one catalyst selected from quaternary ammonium salts and/or quaternary phosphonium salts with halogens, hydroxides, alcoholates or organic or inorganic acid anions as counter-ion; and d) 0.1 to 5 wt.% of at least one cocatalyst, selected from dl) at least one epoxide and/or d2) at least one metal acetylacetonate and/or quaternary ammonium acetylacetonate and/or quaternary phosphonium acetylacetonate; and e) optionally auxiliary agents and additives known from polyurethane chemistry, is used so that the two components a) and b) are present in the ratio such that for each hydroxyl group of the component b) 0.3 to 1 uretdione group of the component a) is consumed, WO 2012/038200 PCT/EP2011/064895 12 preferably 0.6 to 0.9. The latter corresponds to a NCO/OH ratio of 0.6 to 2 to 1 or 1.2 to 1.8 to 1 respectively. These highly reactive polyurethane compositions used according to the invention are cured at temperatures of 100 to 1600C and designated as modification ll. Suitable highly reactive uretdione group-containing polyurethane compositions according to the invention contain mixtures of temporarily deactivated, that is uretdione group-containing (internally blocked) di- or polyisocyanates, also described as curing agents a), and the catalysts c) and d) contained according to the invention and optionally in addition a polymer (binder) having functional groups - reactive towards NCO groups - also described as resin b). The catalysts ensure curing of the uretdione group-containing polyurethane compositions at low temperature. The uretdione group-containing polyurethane compositions are thus highly reactive. As component a) and b), those such as described above are used. As catalysts under c), quaternary ammonium salts, preferably tetraalkylammonium salts and/or quaternary phosphonium salts with halogens, hydroxides, alcoholates or organic or inorganic acid anions as counter-ion, are used. Examples of these are: Tetramethylammonium formate, tetramethylammonium acetate, tetramethylammonium propionate, tetramethylammonium butyrate, tetramethylammonium benzoate, tetraethylammonium formate, tetraethylammonium acetate, tetraethylammonium propionate, tetraethylammonium butyrate, tetraethylammonium benzoate, tetrapropylammonium formate, tetrapropylammonium acetate, tetrapropylammonium propionate, tetrapropylammonium butyrate, tetrapropylammonium benzoate, tetrabutylammonium formate, tetrabutylammonium acetate, tetrabutylammonium propionate, tetrabutylammonium butyrate and tetrabutylammonium benzoate and tetrabutylphosphonium acetate, tetrabutylphosphonium formate and ethyltriphenylphosphonium acetate, tetrabutylphosphonium benzotriazolate, tetraphenylphosphonium phenolate and trihexyltetradecylphosphonium decanoate, methyltributylammonium hydroxide, methyltriethylammonium hydroxide, tetramethylammonium hydroxide, tetraethylammonium hydroxide, tetrapropylammonium hydroxide, tetrabutylammonium hydroxide, tetrapentylammonium hydroxide, tetrahexylammonium hydroxide, tetraoctylammonium hydroxide, tetradecylammonium hydroxide, tetradecyltrihexylammonium hydroxide, tetraoctadecylammonium hydroxide, benzyltrimethylammonium hydroxide, benzyltriethylammonium hydroxide, tri- WO 2012/038200 PCT/EP2011/064895 13 methylphenylammonium hydroxide, triethylmethylammonium hydroxide, tri methylvinylammonium hydroxide, methyltributylammonium methanolate, methyltriethylammonium methanolate, tetramethylammonium methanolate, tetraethylammonium methanolate, tetrapropylammonium methanolate, tetrabutylammonium methanolate, tetrapentylammonium methanolate, tetrahexylammonium methanolate, tetraoctylammonium methanolate, tetradecylammonium methanolate, tetradecyltrihexylammonium methanolate, tetraoctadecylammonium methanolate, benzyltrimethylammonium methanolate, benzyltriethylammonium methanolate, trimethylphenylammonium methanolate, triethylmethylammonium methanolate, trimethylvinylammonium methanolate, methyltributylammonium ethanolate, methyltriethylammonium ethanolate, tetramethylammonium ethanolate, tetraethylammonium ethanolate, tetrapropylammonium ethanolate, tetrabutylammonium ethanolate, tetrapentylammonium ethanolate, tetrahexylammonium ethanolate, tetraoctylammonium methanolate, tetradecylammonium ethanolate, tetradecyltrihexylammonium ethanolate, tetraoctadecylammonium ethanolate, benzyltrimethylammonium ethanolate, benzyltriethylammonium ethanolate, trimethylphenylammonium ethanolate, triethylmethylammonium ethanolate, trimethylvinylammonium ethanolate, methyltributylammonium benzylate, methyltriethylammonium benzylate, tetramethylammonium benzylate, tetraethylammonium benzylate, tetrapropylammonium benzylate, tetrabutylammonium benzylate, tetrapentylammonium benzylate, tetrahexylammonium benzylate, tetraoctylammonium benzylate, tetradecylammonium benzylate, tetradecyltrihexylammonium benzylate, tetraoctadecylammonium benzylate, benzyltrimethylammonium benzylate, benzyltriethylammonium benzylate, trimethylphenylammonium benzylate, triethylmethylammonium benzylate, trimethylvinylammonium benzylate, tetramethylammonium fluoride, tetraethylammonium fluoride, tetrabutylammonium fluoride, tetraoctylammonium fluoride, benzyltrimethylammonium fluoride, tetrabutylphosphonium hydroxide, tetrabutylphosphonium fluoride, tetrabutylammonium chloride, tetrabutylammonium bromide, tetrabutylammonium iodide, tetraethylammonium chloride, tetraethylammonium bromide, tetraethylammonium iodide, tetramethylammonium chloride, tetramethylammonium bromide, tetramethylammonium iodide, benzyltrimethylammonium chloride, benzyltriethylammonium chloride, benzyltripropylammonium chloride, benzyltributylammonium chloride, methyltributylammonium chloride, methyltripropylammonium chloride, methyltriethylammonium chloride, methyltriphenylammonium chloride, phenyltrimethylammonium chloride, benzyltrimethylammonium bromide, benzyltriethylammonium bromide, WO 2012/038200 PCT/EP2011/064895 14 benzyltripropylammonium bromide, benzyltributylammonium bromide, methyltributylammonium bromide, methyltripropylammonium bromide, methyltriethylammonium bromide, methyltriphenylammonium bromide, phenyltrimethylammonium bromide, benzyltrimethylammonium iodide, benzyltriethylammonium iodide, benzyltripropylammonium iodide, benzyltributylammonium iodide, methyltributylammonium iodide, methyltripropylammonium iodide, methyltriethylammonium iodide, methyltriphenylammonium iodide and phenyltrimethylammonium iodide, methyltributylammonium hydroxide, methyltriethylammonium hydroxide, tetramethylammonium hydroxide, tetraethylammonium hydroxide, tetrapropylammonium hydroxide, tetrabutylammonium hydroxide, tetrapentylammonium hydroxide, tetrahexylammonium hydroxide, tetraoctylammonium hydroxide, tetradecylammonium hydroxide, tetradecyltrihexylammonium hydroxide, tetraoctadecylammonium hydroxide, benzyltrimethylammonium hydroxide, benzyltriethylammonium hydroxide, trimethylphenylammonium hydroxide, triethylmethylammonium hydroxide, trimethylvinylammonium hydroxide, tetramethylammonium fluoride, tetraethylammonium fluoride, tetrabutylammonium fluoride, tetraoctylammonium fluoride and benzyltrimethylammonium fluoride. These catalysts can be added alone or in mixtures. Tetraethylammonium benzoate and/or tetrabutylammonium hydroxide are preferably used. The content of catalysts c) can be 0.1 to 5 wt.%, preferably from 0.3 to 2 wt.%, based on the total formulation of the matrix material. One modification according to the invention also includes the binding of such catalysts c) to the functional groups of the polymers b). Apart from this, these catalysts can be surrounded by an inert shell and be enapsulated thereby. As cocatalysts dl) epoxides are used. Possible here are for example glycidyl ethers and glycidyl esters, aliphatic epoxides, diglycidyl ethers based on bisphenol A and glycidyl methacrylates. Examples of such epoxides are triglycidyl isocyanurate (TGIC, trade name ARALDIT 810, Huntsman), mixtures of diglycidyl terephthalate and triglycidyl trimellitate (trade name ARALDIT PT 910 and 912, Huntsman), glycidyl esters of versatic acid (trade name KARDURA E10, Shell), 3,4-epoxycyclohexylmethyl 3 ',4'-epoxycyclohexanecarboxylate (ECC), diglycidyl ethers based on bisphenol A (trade name EPIKOTE 828, Shell), ethylhexyl glycidyl ether, butyl glycidyl ether, pentaerythritol tetraglycidyl ether (trade name POLYPOX R 16, WO 2012/038200 PCT/EP2011/064895 15 UPPC AG) and other polypox types with free epoxy groups. Mixtures can also be used. Preferably used ARALDIT PT 910 and 912 are used. As cocatalysts d2), metal acetylacetonates are possible. Examples of these are zinc acetylacetonate, lithium acetylacetonate and tin acetylacetonate, alone or in mixtures. Zinc acetylacetonate is preferably used. As cocatalysts d2), quaternary ammonium acetylacetonates or quaternary phosphonium acetylacetonates are also possible. Examples of such catalysts are tetramethylammonium acetylacetonate, tetraethylammonium acetylacetonate, tetrapropylammonium acetylacetonate, tetrabutylam monium acetylacetonate, benzyltrimethylammonium acetylacetonate, benzyltriethylammonium acetylacetonate, tetramethylphosphonium acetylacetonate, tetraethylphosphonium acetylacetonate, tetrapropylphosphonium acetylacetonate, tetrabutylphosphonium acetylacetonate, benzyltrimethylphosphonium acetylacetonate and benzyltriethylphosphonium acetylacetonate. Particularly preferably, tetraethylammonium acetylacetonate and/or tetrabutylammonium acetylacetonate are used. Of course mixtures of such catalysts can also be used. The quantity of cocatalysts d1l) and/or d2) can be from 0.1 to 5 wt.%, preferably from 0.3 to 2 wt.%, based on the total formulation of the matrix material. By means of the highly reactive and thus low temperature curing polyurethane compositions B) used according to the invention, at 100 to 160 0 C curing temperature not only can energy and curing time be saved, but many temperature-sensitive supports can also be used. In the context of this invention, highly reactive (modification 1l) means that the uretdione group containing polyurethane compositions used according to the invention cure at temperatures from 100 to 1600C, depending on the nature of the support. This curing temperature is preferably 120 to 1500C, particularly preferably from 130 to 1400C. The time for the curing of the polyurethane composition used according to the invention lies within from 5 to 60 minutes. The highly reactive uretdione group-containing polyurethane compositions B) used according to he invention provide very good flow and hence good impregnation behaviour and in the cured WO 2012/038200 PCT/EP2011/064895 16 state excellent chemicals resistance. In addition, with the use of aliphatic crosslinking agents (e.g. IPDI or H 12 MDI) good weather resistance is also achieved. Suitable pigments are in principle all known pigments. The pigments from the known classes of the natural and synthetic inorganic pigments are employed. Useful natural pigments include earth colours, for example, green earth, yellow ochre or umber, and also mineral colours, for example iron oxides, malachite or cinnabar. Also suitable are inorganic synthetic pigments, for example carbon black, chromium pigments, cobalt pigments, iron pigments, ultramarine blue, or white pigments, for example titanium dioxide. Likewise suitable are natural organic pigments and synthetic organic pigments such as azo pigments (brilliant yellow, permanent red), polycyclic pigments (phthalocyanine blue, heliogen green) or diketopyrrolopyrrole pigments. Also suitable are metal effect pigments or pearlescent pigments. Examples of such pigments are: Prussian blue (pigment blue 27 C.1. 77510), brilliant yellow (pigment yellow 74 C.I. 11741), cadmium yellow (pigment yellow 35 C.I. 77205), cadmium red (pigment red 108 C.I. 77202), chromium oxide green (pigment green 17 C.I. 77288), cobalt blue (pigment blue 28 C.I. 77346), cobalt blue turquoise light (pigment blue 36 C.I. 77343), cobalt violet light (pigment violet 49 C.1. 77362), iron oxide black (pigment black 11 C.1. 77499), irgazine red (pigment red 254 C.1. 56110), manganese violet (pigment violet 16 C.1. 77742), phthalocyanine blue (org.) (pigment blue 15 C.I. 74160), titanium white (pigment white C.. 77891), ultramarine blue (pigment blue 29 C.I. 77007), ultramarine red A (pigment red 259 C.I. 77007), umber (pigment brown 7 C.I. 77491). Suitable dyes are all known dyes, especially reactive dyes, disperse dyes, pigment dyes, acid dyes, developing dyes, cationic or basic dyes, coupling dyes, mordant dyes, vat dyes, metal complex dyes, substantive dyes. Important classes of dyes useable in the context of the invention are anthraquinone dyes, azo dyes, dioxazine dyes, indigo dyes, nitro dyes, nitroso dyes, phthalocyanine dyes, sulphur dyes, triphenylmethane dyes.

WO 2012/038200 PCT/EP2011/064895 17 Dyes and pigments especially suitable for powder coating applications are detailed, for example, in the documents from Clariant "Colorants for Powder Coatings" (2005) and from BASF "Colorants and additives from BASF for powder coatings" (2008). Overall, preference is given to pigment formulations since dyes have an at least limited light stability or weathering stability which limits direct outdoor use of the composite components produced from the correspondingly coloured prepregs according to the invention. The dyes are present in an amount of 15 up to % by weight in the matrix material B). Pigments are present in an amount of 0.5 up to 20% by weight in the matrix material B). The production of the matrix material can be effected as follows: the homogenization of all components for the production of the polyurethane composition B) can be effected in suitable units, such as for example heatable stirred vessels, kneaders, or even extruders, during which temperature upper limits of 120 to 130 0 C should not be exceeded. The mixing of the individual components is preferably effected in an extruder at temperatures which are above the melting ranges of the individual components, but below the temperature at which the crosslinking reaction starts. Use directly from the melt or after cooling and production of a powder is possible thereafter. The production of the polyurethane composition B) can also be effected in a solvent by mixing in the aforesaid units. Next, depending on the process, the matrix material B) with the support A) is processed into the prepregs. The prepregs according to the invention and also the composite components have a fibre content by volume of greater than 50%, preferably of greater than 50 - 70%, particularly preferably of 50 to 65%. The reactive or highly reactive polyurethane compositions used according to the invention as matrix material essentially consist of a mixture of a reactive resin and a curing agent. After melt homogenization, this mixture has a Tg of at least 40 0 C and as a rule reacts only above 160 0 C in the case of the reactive polyurethane compositions, or above 1 00*C in the case of the highly reactive polyurethane compositions, to give a crosslinked polyurethane and thus forms the matrix of the composite. This means that the prepregs according to the invention after their WO 2012/038200 PCT/EP2011/064895 18 production are made up of the support and the applied reactive polyurethane composition as matrix material, which is present in noncrosslinked but reactive form. The prepregs are thus storage-stable, as a rule for several days and even weeks and can thus at any time be further processed into composites. This is the essential difference from the 2 component systems already described above, which are reactive and not storage-stable, since after application these immediately start to react and crosslink to give polyurethanes. The production of the prepregs according to the invention can be performed by means of the known plants and equipment by reaction injection moulding (RIM), reinforced reaction injection moulding (RRIM), pultrusion processes, by application of the solution in a cylinder mill or by means of a hot doctor knife, or other processes. Also subject matter of the invention is the use of the prepregs, in particular with fibrous supports of glass, carbon or aramid fibres. Also subject matter of the invention is the use of the prepregs produced according to the invention, for the production of composites in boat and shipbuilding, in aerospace technology, in automobile manufacture, and for two-wheel vehicles, preferably motorcycles and bicycles, and in the automotive, construction, medical engineering and sport fields, electrical and electronics industry, and power generating plants, e.g. for rotor blades in wind power plants. Also subject matter of the invention are the composite components produced from the prepregs produced according to the invention.

WO 2012/038200 PCT/EP2011/064895 19 Examples Reactive polyurethane composition A reactive polyurethane composition with the following formula was used for the production of the prepregs and the composites. Example I Formulation [Modification 1] (according to the invention) in wt.% VESTAGON BF 1321 32.02 (uretdione group-containing curing agent component a)), Evonik Degussa Reafree 17014 46.86 (OH-functional polyester resin component, from Cray Valley) Reafree 17091 15.62 (OH-functional polyester resin component from Cray Valley) Resiflow PV 88 1.00 (levelling agent; from Worl6e) Benzoin, 0.50 (degassing aid, from Aldrich) Colortherm Yellow 10 4.00 (micronized pigment for plastics applications, from Lanxess) NCO:OH ratio 0.9:1 The milled ingredients from the table are intimately mixed in a premixer and then homogenized in the extruder up to a maximum of 1300C. This reactive polyurethane composition can then after milling be used for the production of the prepregs by the powder impregnation process. For the direct melt impregnation process, the homogenized melt mixture produced in the extruder can be used directly. For the solvent-based process, no upstream melt homogenization is required.

WO 2012/038200 PCT/EP2011/064895 20 DSC measurements The DSC tests (glass transition temperature determinations and enthalpy of reaction measurements) are performed with a Mettler Toledo DSC 821 e as per DIN 53765. The glass transition temperature of the extrudate was determined to 620C; the reaction enthalpy for the crosslinking reaction in the fresh state was 65.5 J/g. After the crosslinking of the matrix of the prepreg, the glass transition temperature rose to 800C and no heat flow for crosslinking was detectable any longer. For the results see Figure 1. Glass fibre scrims and glass fibre fabrics used: The following glass fibre scrims and glass fibre fabrics were used in the examples and are referred to below as type I and type 11. Type I is a linen E glass fabric 281 L Art. No. 3103 from "Schl6sser & Cramer". The fabric has an areal weight of 280 g/m 2 . Type 11 GBX 600 Art. No. 1023 is a sewn biaxial E glass scrim (-45/+45) from "Schl6sser & Cramer". This should be understood to mean two layers of fibre bundles which lie one over the other and are set at an angle of 90 degrees to one another. This structure is held together by other fibres, which do not however consist of glass. The surface of the glass fibres is treated with a standard size which is aminosilane-modified. The scrim has an areal weight of 600 g/m 2 . Production of the prepregs The production of the prepregs is effected by direct melt impregnation processes according to DE 102010029355. Storage stability of the prepregs The storage stability of the prepregs was determined from the glass transition temperatures and the enthalpies of reaction of the crosslinking reaction by means of DSC studies. The crosslinking capacity of the PU prepregs is not impaired by storage at room temperature for a period of 5 weeks.

WO 2012/038200 PCT/EP2011/064895 21 Time (days Tg [*C] storage time) 2 62 14 64 28 62 35 63 enthalpy of Time (days curing [J/g] storage time) 2 65 14 67 28 67 35 66 Composite Component Production The composite components are produced on a composite press by a compression technique known to those skilled in the art. The homogeneous prepregs produced by direct impregnation were compressed into composite materials on a benchtop press. This benchtop press is the Polystat 200 T from the firm Schwabenthan, with which the prepregs are compressed to the corresponding composite sheets at temperatures between 120 and 2000C. The pressure is varied between normal pressure and 450 bar. Dynamic compression, i.e. alternating applications of pressure, can prove advantageous for the crosslinking of the fibres depending on the component size, thickness and polyurethane composition and hence the viscosity setting at the processing temperature. In one example, the temperature of the press is increased from 900C during the melting phase to 11 0*C, the pressure is increased to 440 bar after a melting phase of 3 minutes and then dynamically varied (7 times each of 1 minute duration) between 150 and 440 bar, during which the temperature is continuously increased to 1400C. Next the temperature is raised to 1800C and at the same time the pressure is held at 350 bar until the removal of the composite component from the press after 30 minutes height. The hard, rigid, chemicals resistant and impact resistant composite components (sheet products) with a fibre volume content of > 50 % are tested for the degree of curing (determination by DSC). The determination of the glass WO 2012/038200 PCT/EP2011/064895 22 transition temperature of the cured matrix indicates the progress of the crosslinking at different curing temperatures. With the polyurethane composition used, the crosslinking is complete after ca. 25 minutes, and then an enthalpy of reaction for the crosslinking reaction is also no longer detectable.

Claims

1. Prepregs, essentially made up of A) at least one fibrous support and B) with a matrix material of at least one polyurethane composition B) containing uretdione groups, essentially containing a) at least one uretdione group-containing curing agent, based on polyaddition compounds from aliphatic, (cyclo)aliphatic or cycloaliphatic uretdione group containing polyisocyanates and hydroxyl group-containing compounds, wherein the curing agent is in solid form below 40*C and in liquid form above 125*C, and has a free NCO content of less than 5 wt.% and a uretdione content of 3 - 25 wt.%, b) at least one hydroxyl group-containing polymer which is in solid form below 400C and in liquid form above 1250C and has an OH number between 20 and 200 mg KOH/gram, c) optionally at least one catalyst, and d) optionally auxiliary agents and additives known from polyurethane chemistry, so that the two components a) and b) are present in the ratio such that for each hydroxyl group of the component b) 0.3 to 1 uretdione group of the component a) is consumed, preferably 0.45 to 0.55, and wherein the matrix material additionally comprises 1. pigments having a particle diameter of < 150 nm and/or

2. dyes. 2. Prepregs according to Claim 1, wherein the matrix material B) has a Tg of at least 400C.

3. Prepregs according to at least one of the previous claims, characterized in that the prepregs have a fibre content by volume of greater than 50%, preferably of greater than 50 to 70%, particularly preferably of 50 to 65%.

4. Prepregs according to at least one of the previous claims, characterized in that the pigments present are natural and/or synthetic inorganic pigments. 24

5. Prepregs according to at least one of the previous claims, characterized in that dyes selected from reactive dyes, disperse dyes, pigment dyes, acid dyes, developing dyes, cationic or basic dyes, coupling dyes, mordant dyes, vat dyes, metal complex dyes, substantive dyes are present.

6. Prepregs according to at least one of the previous claims, characterized in that polymers b) with hydroxyl groups, amino groups and thiol groups, in particular polyesters, polyethers, polyacrylates, polycarbonates and polyurethanes with an OH number of 20 to 500 mg KOH/gram and an average molecular weight of 250 to 6000 g/mole are used.

7. Prepregs according to at least one of the previous claims, characterized in that di- or polyisocyanates, selected from isophorone diisocyanate (IPDI), hexamethylene diisocyanate (HDI), diisocyanatodicyclohexylmethane (H12MDI), 2-methylpentane diisocyanate (MPDI), 2,2,4-trimethylhexamethylene diisocyanate/2,4,4-trimethyl hexamethylene diisocyanate (TMDI) and/or norbornane diisocyanate (NBDI), particularly preferably IPDI, HDI, TMDI and/or H 12 MDI, wherein the isocyanurates are also usable, are used as starting compounds for the component a).

8. Prepregs according to at least one of the previous claims, characterized in that external blocking agents selected from ethyl acetoacetate, diisopropylamine, methyl ethyl ketoxime, diethyl malonate, E-caprolactam, 1,2,4-triazole, phenol or substituted phenols and/or 3,5-dimethylpyrazole are used for the blocking of a).

9. Prepregs according to at least one of the previous claims, characterized in that IPDI adducts, the isocyanurate groups and E-caprolactam blocked isocyanate structures are used as component a).

10. Prepregs according to at least one of the previous claims, characterized in that the reactive polyurethane compositions B) contain additional catalysts, preferably dibutyltin dilaurate, zinc octoate, bismuth neodecanoate, and/or tertiary amines, preferably 1,4-diazabicyclo[2.2.2.]octane, in quantities of 0.001 - 1 wt.%.

11. Prepregs according to at least one of Claims 1 to 9, with at least one highly reactive powdery uretdione group-containing polyurethane composition B) as matrix material, essentially containing a) at least one uretdione group-containing curing agent and b) optionally at least one polymer with functional groups reactive towards NCO groups; c) 0.1 to 5 wt.% of at least one catalyst selected from quaternary ammonium salts and/or quaternary phosphonium salts with halogens, hydroxides, alcoholates or organic or inorganic acid anions as counter-ion; and d) 0.1 to 5 wt.% of at least one cocatalyst, selected from dl) at least one epoxide and/or d2) at least one metal acetylacetonate and/or quaternary ammonium acetylacetonate and/or quaternary phosphonium acetylacetonate; and e) optionally auxiliary agents and additives known from polyurethane chemistry.

12. Prepregs according to at least one of the previous Claims 1 to 9 or 11 with at least one highly reactive powdery uretdione group-containing polyurethane composition B) as matrix material, essentially containing a) at least one uretdione group-containing curing agent, based on polyaddition compounds from aliphatic, (cyclo)aliphatic or cycloaliphatic uretdione group containing polyisocyanates and hydroxyl group-containing compounds, wherein the curing agent is in solid form below 40*C and in liquid form above 125*C and has a free NCO content of less than 5 wt.% and a uretdione content of 3 - 25 wt.% , b) at least one hydroxyl group-containing polymer which is in solid form below 40*C and in liquid form above 125*C and has an OH number between 20 and 200 mg KOH/gram; 26 c) 0.1 to 5 wt.% of at least one catalyst selected from quaternary ammonium salts and/or quaternary phosphonium salts with halogens, hydroxides, alcoholates or organic or inorganic acid anions as counter-ion; and d) 0.1 to 5 wt.% of at least one cocatalyst, selected from dl) at least one epoxide and/or d2) at least one metal acetylacetonate and/or quaternary ammonium acetylacetonate and/or quaternary phosphonium acetylacetonate; and e) optionally auxiliary agents and additives known from polyurethane chemistry, so that the two components a) and b) are present in the ratio such that for each hydroxyl group of the component b) 0.3 to 1 uretdione group of the component a) is consumed, preferably 0.6 to 0.9.

13. Use of the prepregs according to at least one of the previous Claims 1 to 12, in particular with fibrous supports of glass, carbon or aramid fibres.

14. Use of the prepregs according to at least one of Claims 1 to 12 for the production of composites in boat and ship building, in aerospace technology, in automobile manufacture, for two-wheel vehicles preferably motorcycles and bicycles, in the automotive, construction, medical technology and sport fields, electrical and electronics industry and power generation plants, such as for rotor blades in wind power plants.

15. Composite components produced from prepregs according to at least one of Claims 1 to 12. Evonik Degussa GmbH Patent Attorneys for the Applicant/Nominated Person SPRUSON & FERGUSON