Title of Invention	"COMPOSITION"
Abstract	Composition consisting of (A) 4 to 80 parts by wt. of a polyalkylene terephthalate, (B) 10 to 90 parts by wt. of a aromatic polycarbonate, (C) 1.5 to 30 parts by wt. of a graft polymer based on polybutadiene as the rubber component, (D) 1.5 to 30 parts by wt. of a graft polymer based on acrylates as the rubber component, (E) 0.01 to 5 parts by wt. of UV stabilizers of the kind such as herein described, (F) 0.01 to 10 parts by wt. of colouring agent of the kind such as herein described, (G) 0 to 5 parts by wt. of hydrolysis stabilizers of the kind such as herein described, (H) 0 to 54 parts by wt. of a particulate mineral filler of the kind such as herein described, (I) 0 to 10 parts by wt. of further additives of the kind such as herein described.

Title of Invention

"COMPOSITION"

Abstract

Composition consisting of (A) 4 to 80 parts by wt. of a polyalkylene terephthalate, (B) 10 to 90 parts by wt. of a aromatic polycarbonate, (C) 1.5 to 30 parts by wt. of a graft polymer based on polybutadiene as the rubber component, (D) 1.5 to 30 parts by wt. of a graft polymer based on acrylates as the rubber component, (E) 0.01 to 5 parts by wt. of UV stabilizers of the kind such as herein described, (F) 0.01 to 10 parts by wt. of colouring agent of the kind such as herein described, (G) 0 to 5 parts by wt. of hydrolysis stabilizers of the kind such as herein described, (H) 0 to 54 parts by wt. of a particulate mineral filler of the kind such as herein described, (I) 0 to 10 parts by wt. of further additives of the kind such as herein described.

Full Text	The present invention relates to composition. The present invention relates to coloured, weathering-stabilized compositions based on impact-modified polyalkylene terephthalate/polycarbonate blends and moulding compositions, semi-finished products and mouldings produced therefrom, whichrare employed, for example, for motor vehicle exterior uses in non-lacquered form or in a form coated only with a transparent clear lacquer. Impact-modified moulding compositions which comprise partly crystalline polyesters, amorphous polycarbonates and graft copolymers are known. Such moulding compositions are employed, for example, in the automobile sector for mouldings such as bumpers, mud guards, radiator grills, headlamp screens, tailgate screens, sills, spoilers, door handles, tank caps, linings, horizontal structural components, such as engine bonnets or roof elements, door modules or the like. Prerequisites for use in motor vehicle applications are a high heat distortion point, high flowability in the melt, good lacquer adhesion, high resistance to chemicals, high rigidity, high dimensional stability and high toughness at low temperatures. Mouldings of impact-modified polyalkylene terephthalate/polycarbonate blends can be coloured by two different methods. Traditionally, the mouldings are lacquered with a colouring lacquer, the so-called base lacquer. The mouldings can optionally moreover have been coated with primer and/or filler before the base lacquer. A transparent clear lacquer can furthermore optionally be applied to the base lacquer. These systems are called top-lacquered systems in the following. In top-lacquered systems the intrinsic colour of the moulding compositions is substantially irrelevant, since colouring is done by the base lacquer. As an alternative to the top-lacquered systems, there are systems which are called moulded-in colour systems in the following. In moulded-in colour systems the colour of the moulding in use is determined by the intrinsic colour of the moulding composition, that is to say moulded-in colour systems are not lacquered with a primer, filler or colouring base lacquer. However, the moulded-in colour systems can optionally be coated with transparent clear lacquer. The advantage of moulded-in colour systems lies in the saving in costs, since the working steps of priming with primer and/or fillers and of lacquering with colouring base lacquers and the associated drying operations are omitted. The use of mouldings of impact-modified polyalkylene terephthalate/polycarbonate blends in the motor vehicle exterior sector involves high requirements in respect of the weathering resistance of the material of the mouldings. In this context, the resistance to photooxidation by UV irradiation (called UV stability in the following) and the resistance of the materials to hydrolysing environmental influences (called stability to hydrolysis in the following) are of central importance. hi top-lacquered systems the harmful UV rays are largely kept back by the base lacquer. On the other hand, in moulded-in colour systems there is no UV-blocking function of a covering base lacquer. At best a UV-absorbing clear lacquer can hold off the majority of the harmful UV radiation in moulded-in colour systems. Nevertheless, moulding compositions which are based on moulded-in colour systems must have a high UV stability, and for this reason impact modifiers based on rubbers with conjugated dienes, such as, for example, butadiene in ABS or MBS rubbers, cannot be employed alone. Weathering-stable PC/polyester blends therefore employ, for example, acrylate rubbers, as has been described in DE-A 33 02 124. EP-B 0 787 769 describes the use of PC/polyester blends with a combination of AES and acrylate rubbers to obtain moulding compositions of improved stability to weathering and good toughness. The stability to hydrolysis of impact-modified polyalkylene terephthalate/polycarbonate blends is required in particular if the mouldings of these materials are employed under conditions with a high outside temperature and high atmospheric humidity during the life of the motor vehicle. US-A 5 354 791 describes the use of epoxide-substituted polyalkylene terephthalate moulding compositions in combination with metal-containing phosphorus compounds in impact-modified polyalkylene terephthalate/polycarbonate blends to improve the stability to hydrolysis. The improvement in the stability to hydrolysis is described here by the small change in the melt viscosity after storage of the material at 110 °C in water in an autoclave. The UV resistance and the nature of the surface are not the content of US-A 5 354 791. In moulded-in colour systems, however, in addition to the stability to weathering the ability to be coloured homogeneously is also of very great importance. Precisely in the case of impact-modified PC/polyester blends with weathering-resistant acrylate impact modifiers, in the case of injection mouldings undesirable colour inhomogeneities occur, in which periodically recurring regions coloured less, which have an optically brighter effect, with more deeply coloured regions, which have an optically darker or more colour-intensive effect, are formed perpendicular to the direction of flow during the injection moulding operation, these also being called tiger stripes. For mouldings which are perceived visually by the user in the end use, such as, for example, the motor vehicle exterior skin - such as e.g. mud guards, bumpers, tailgates, headlamp screens, spoilers, air intake grills, engine bonnets, car roofs - motor vehicle interiors, electrical housings or electronics housings, these tiger stripe effects are unacceptable. The object was to develop homogeneously coloured impact-modified polyalkylene terephthalate/polycarbonate moulding compositions of improved weathering resistance for uses in so-called moulded-in colour systems. Increased requirements in respect of homogeneous colouring of the moulding compositions or mouldings are imposed on moulded-in colour systems, since the colouring of the moulding composition is responsible at the same time for the colour appearance of the finished moulding in use. It has now been found, surprisingly, that moulding compositions based on polyalkylene terephthalate/polycarbonate achieve the object described if at least two different systems based on graft copolymer compositions based on acrylates on the one hand and based on butadiene on the other hand are employed as the impact modifier in combination with stabilizers for increasing the UV resistance and for improving the resistance to hydrolysis. The mouldings from the compositions according to the invention are distinguished by a homogeneous appearance and homogeneous colour impression of the surface and excellent stability to weathering. The moulding compositions according to the invention are moreover distinguished by a high heat distortion point, good flowability in the melt, good lacquer adhesion, high resistance to chemicals, high rigidity, high dimensional stability and high toughness at low temperatures. The invention provides compositions comprising A) 4 to 80 parts by wt, preferably 10 to 60 parts by wt., particularly preferably 12 to 50 parts by wt., in particular 19 to 40 parts by wt. of at least one polyalkylene terephthalate, preferably a polyethylene terephthalate or a polybutylene terephthalate, particularly preferably a polybutylene terephthalate, B) 10 to 90 parts by wt., preferably 20 to 80 parts by wt., particularly preferably 25 to 60 parts by wt., in particular 30 to 60 parts by wt. of at least one aromatic polycarbonate, C) 1.5 to 30 parts by wt., preferably 3 to 25 parts by wt., particularly preferably 4 to 20 parts by wt., in particular 5 to 15 parts by wt. of at least one graft polymer based on rubber-elastic olefinically unsaturated olefin (co)polymers, preferably polybutadiene, as the rubber component, D) 1.5 to 30 parts by wt., preferably 3 to 25 parts by wt., particularly preferably 4 to 20 parts by wt., in particular 5 to 15 parts by wt. of at least one graft polymer based on acrylates as the rubber component, E) 0.01 to 5 parts by wt., preferably 0.05 to 3 parts by wt., particularly preferably 0.1 to 1 part by wt. of a UV stabilizer, F) 0.01 to 10 parts by wt., preferably 0.05 to 6 parts by wt., particularly preferably 0.1 to 3 parts by wt. of colouring agent, G) 0 to 5 parts by wt., preferably 0.05 to 3 parts by wt., particularly preferably 0.1 to 2 parts by wt. of hydrolysis stabilizers, preferably based on epoxide compounds, H) 0 to 54 parts by wt., preferably 3 to 34 parts by wt., particularly preferably 6 to 25, in particular 8 to 21 parts by wt. of at least one particulate mineral filler, I) 0 to 10 parts by wt., preferably 0.05 to 3 parts by wt., particularly preferably 0.1 to 0.9 part by wt. of further additives. According to the invention, the compositions comprise as component A one or a mixture of two or more different polyalkylene terephthalates. Polyalkylene terephthalates in the context of the invention are polyalkylene terephthalates which are derived from terephthalic acid (or its reactive derivatives) and alkanediols, for example based on ethylene glycol, propylene glycol or butanediol. According to the invention, preferably polybutylene terephthalate, polytrimethylene terephthalate and/or polyethylene terephthalate, particularly preferably polybutylene terephthalate and/or polyethylene terephthalate, most preferably polybutylene terephthalate are employed as component A. Polyalkylene terephthalates in the context of the invention are reaction products of aromatic dicarboxylic acids or their reactive derivatives (e.g. dimethyl esters or anhydrides) and aliphatic, cycloaliphatic or araliphatic diols and mixtures of these reaction products. Preferred polyalkylene terephthalates can be prepared from terephthalic acid (or its reactive derivatives) and aliphatic or cycloaliphatic diols having 2 to IOC atoms by known methods (Kunststoff-Handbuch, vol. VIII, p. 695 et seq., Karl-Hanser-Verlag, Munich 1973). Preferred polyalkylene terephthalates contain at least 80 mol%, preferably 90 mol%, based on the dicarboxylic acid, of terephthalic acid radicals and at least 80 mol%, preferably at least 90 mol%, based on the diol component, of radicals of ethylene glycol and/or propane- 1,3-diol and/or butane-1,4-diol. The preferred polyalkylene terephthalates can contain, in addition to terephthalic acid radicals, up to 20 mol% of radicals of other aromatic dicarboxylic acids having 8 to 14 C atoms or aliphatic dicarboxylic acids having 4 to 12 C atoms, such as radicals of phthalic "acid, isophthalic acid, naphthalene-2,6-dicarboxylic acid, 4,4'-diphenyldicarboxylic acid, succinic acid, adipic acid, sebacic acid, azelaic acid, cyclohexanediacetic acid or cyclohexanedicarboxylic acid. The preferred polyalkylene terephthalates can contain, in addition to radicals of ethylene glycol or propane-1,3-diol or butane-1,4-diol, up to 20 mol% of other aliphatic diols having 3 to 12 C atoms or cycloaliphatic diols having 6 to 21 C atoms, e.g. radicals of propane-1,3-diol, 2-ethylpropane-1,3-diol, neopentylglycol, pentane-l,5-diol, hexane-l,6-diol, cyclohexane-1,4-dimethanol, 3-methylpentane-2,4-diol, 2-methylpentane-2,4-diol, 2,2,4-trimethylpentane-1,3-diol and -1,6-diol, 2- ethylhexane-l,3-diol,2,2-diethylpropane-l,3-diol, hexane-2,5-diol, hydroxyethoxy)-benzene, 2,2-bis-(4-hydroxycyclohexyl)-propane, 2,4-dihydroxy-1,1,3,3-tetramethyl-cyclobutane, 2,2-bis-(3-/3-hydroxyethoxyphenyl)-propane and 2,2-bis-(4-hydroxypropoxyphenyl)-propane.The polyalkylene terephthalates can be branched by incorporation of relatively small amounts of 3- or 4-hydric alcohols or 3- or 4-basic carboxylic acids, such as are described e.g. in DE-A 19 00 270 and US-A 3 692 744. Examples of preferred branching agents are trimesic acid, trimellitic acid, trimethylolethane and -propane and pentaerythritol. It is advisable to use not more than 1 mol% of the branching agent, based on the acid component. Polyalkylene terephthalates which have been prepared solely from terephthalic acid and reactive derivatives thereof (e.g. dialkyl esters thereof) and ethylene glycol and/or propane-l,3-diol and/or butane-1,4-diol (polyethylene terephthalate and polybutylene terephthalate) and mixtures of these polyalkylene terephthalates are particularly preferred. Copolyesters which are prepared from at least two of the abovementioned acid components and/or from at least two of the abovementioned alcohol components are also preferred polyalkylene terephthalates, and particularly preferred copolyesters are poly-(ethylene glycol/butane- 1,4-diol) terephthalates. The polyalkylene terephthalates in general have an intrinsic viscosity of approx. 0.4 to 1.5, preferably 0.5 to 1.3, in each case measured in phenol/o-dichlorobenzene (1:1 parts by wt.) at 25 °C. The polyalkylene terephthalates to be employed according to the invention can preferably also be employed in a mixture with other polyesters and/or further polymers. Particularly preferably, mixtures of polyalkylene terephthalates with other polyesters, very particularly preferably mixtures of polybutylene terephthalate with polyethylene terephthalate are employed. Conventional additives, such as e.g. mould release agents, stabilizers and/or flow agents, can be added to the mixtures in the melt or applied to the surface. According to the invention, the compositions according to the invention comprise as component B a polycarbonate or a mixture of polycarbonates. Preferred polycarbonates are those homopolycarbonates and copolycarbonates based on the bisphenols of the general formula (I) (Formula Removed) wherein Z is a divalent organic radical having 6 to 30 C atoms which contains one or more aromatic groups. Bisphenols of the formula (la) (Figure Removed) represents a single bond, C1-C5-alkylene, C2-C5-alkylidene, C5-C6-cycloalkylidene, -O-, -SO-, -CO-, -S-, -SO2-, C6-C12-arylene, on to which further aromatic rings optionally containing heteroatoms can be fused,or a radical of the formula (II) or (III) B represents in each case C1-C12-alkyl, preferably methyl, or halogen, preferably chlorine and/or bromine, x in each case independently of one another, represents 0,1 or 2, p represents 1 or 0, R1 and R2 can be chosen individually for each X1 and independently of one another represent hydrogen or C1-C6-alkyl, preferably hydrogen, methyl or ethyl, X1 represents carbon and m represents an integer from 4 to 7, preferably 4 or 5, with the proviso that on at least one atom X1 R1 and R2 simultaneously represent alkyl are preferred. Examples of bisphenols according to the general formula (I) are bisphenols which belong to the following groups: dihydroxydiphenyls, bis-(hydroxyphenyl)-alkanes, bis-(hydroxyphenyl)-cycloalkanes, indanebisphenols, bis-(hydroxyphenyl) sulfides,bis-(hydroxyphenyl) ethers, bis-(hydroxyphenyl) ketones, bis-(hydroxyphenyl) sulfones, bis-(hydroxyphenyl) sulfoxides and α,α1-bis-(hydroxyphenyl)-diisopropylbenzenes. Derivatives of the bisphenols mentioned which are accessible, for example, by alkylation or halogenation on the aromatic rings of the bisphenols mentioned are also examples of bisphenols according to the general formula (I). Examples of bisphenols according to the general formula (I) are, in particular, the following compounds: hydroquinone, resorcinol, 4,4'-dihydroxydiphenyl, bis-(4- hydroxyphenyl) sulfide, bis-(4-hydroxyphenyl) sulfone, bis-(3,5-dimethyl-4- hydroxyphenyl)-methane, bis-(3,5-dimethyl-4-hydroxyphenyl) sulfone, l,l-bis-(3,5- dimethyl-4-hydroxyphenyl)-p/rn-diisopropylbenzene, 1,1 -bis-(4-hydroxyphenyl)-1 - phenyl-ethane, 1,1 -bis-(3,5-dimethyl-4-hydroxyphenyl)-cyclohexane, 1,1 -bis-(4- hydroxyphenyl)-3-methylcyclohexane, 1,1 -bis-(4-hydroxyphenyl)-3,3- dimethylcyclohexane, 1,1 -bis-(4-hydroxyphenyl)-4-methylcyclohexane, 1,1 -bis-(4- hydroxyphenyl)-cyclohexane, 1,1 -bis-(4-hydroxyphenyl)-3,3,5- trimethylcyclohexane, 2,2-bis-(3,5-dichloro-4-hydroxyphenyl)-propane, 2,2-bis-(3- methyl-4-hydroxyphenyl)-propane, 2,2-bis-(3,5-dimethyl-4-hydroxyphenyl)- propane, 2,2-bis-(4-hydroxyphenyl)-propane (i.e. bisphenol A), 2,2-bis-(3-chloro-4-hydroxyphenyl)-propane, 2,2-bis-(3,5-dibromo-4-hydroxyphenyl)-propane, 2,4-bis-(4-hydroxyphenyl)-2-methylbutane, 2,4-bis-(3,5-dimethyl-4-hydroxyphenyl)-2-methylbutane, α,α'-bis-(4-hydroxyphenyl)-o-diisopropylbenzene, α,α'-bis-(4-hydroxyphenyl)-m-diisopropylbenzene (i.e. bisphenol M), α,α'-bis-(4-hydroxyphenyl)-p-diisopropylbenzene and indanebisphenol. Particularly preferred polycarbonates are the homopolycarbonate based on bisphenol A, the homopolycarbonate based on l,l-bis-(4-hydroxyphenyl)-3,3,5-trimethylcyclohexane and the copolycarbonates based on the two monomers bisphenol A and l,l-bis-(4-hydroxyphenyl)-3,3,5-trimethylcyclohexane.The bisphenols described, according to the general formula (I), can be prepared by known processes, e.g. from the corresponding phenols and ketones. The bisphenols mentioned and processes for their preparation belong to the prior art., thus also l,l-bis-(4-hydroxyphenyl)-3,3,5-trimethylcyclohexane and the indanebisphenols. Indanebisphenols can be prepared, for example, from isopropenylphenol or derivatives thereof, or from dimers of isopropenylphenol or derivatives thereof in the presence of a Friedel-Crafts catalyst in organic solvents. Polycarbonates can be prepared by known processes. Suitable processes for the preparation of polycarbonates are, for example, preparation from bisphenols with phosgene by the phase boundary process or from bisphenols with phosgene by the process in a homogeneous phase, the so-called pyridine process, or from bisphenols with carbonic acid esters by the melt transesterification process. These preparation processes are described e.g. in H. Schnell, "Chemistry and Physics of Polycarbonates", Polymer Reviews, volume 9, p. 31-76, Interscience Publishers, New York, London, Sydney, 1964. The melt transesterification process is described, in particular, in H. Schnell, "Chemistry and Physics of Polycarbonates", Polymer Reviews, volume 9, p. 44 to 51, Interscience Publishers, New York, London, Sydney, 1964. Raw materials and auxiliary substances with a low degree of impurities are preferably employed in the preparation of polycarbonate. In the preparation by the melt transesterification process in particular, the bisphenols employed and the carbonic acid derivatives employed should be as free as possible from alkali metal ions and alkaline earth metal ions. Raw materials of such purity are obtainable, for example, by recrystallizing, washing or distilling the carbonic acid derivatives, for example carbonic acid esters, and the bisphenols.The polycarbonates to be employed according to the invention preferably have a weight-average molecular weight (Mw), which can be determined e.g. by ultracentrifugation or scattered light measurement, of 10,000 to 200,000 g/mol. They particularly preferably have a weight-average molecular weight of 12,000 to 80,000 g/mol, especially preferably 20,000 to 35,000 g/mol. The average molecular weight of the polycarbonates to be employed according to the invention can be established, for example, in a known manner by an appropriate amount of chain terminators. The chain terminators can be employed individually or as a mixture of various chain terminators. Suitable chain terminators are both monophenols and monocarboxylic acids. Suitable monophenols are e.g. phenol, p-chlorophenol, p-tert-butylphenol, cumylphenol or 2,4,6-tribromophenol, and long-chain alkylphenols, such as e.g. 4-(l,l,3,3-tetramethylbutyl)-phenol, or monoalkylphenols or dialkylphenols having a total of 8 to 20 C atoms in the alkyl substituents, such as e.g. 3,5-di-tert-butylphenol, p-tert-octylphenol, p-dodecylphenol, 2-(3,5-dimethyl-heptyl)-phenol or 4-(3,5-dimethyl-heptyl)-phenol. Suitable monocarboxylic acids are benzoic acid, alkylbenzoic acids and halogenobenzoic acids. Preferred chain terminators are phenol, p-tert-butylphenol, 4-(l,1,3,3-tetramethylbutyl)-phenol and cumylphenol. The amount of chain terminators to be employed is preferably between 0.25 and 10 mol%, based on the total of the particular bisphenols employed. The polycarbonates to be employed according to the invention can be branched in a known manner, and in particular preferably by incorporation of branching agents which are trifunctional or more than trifunctional. Suitable branching agents are e.g. those having three or more than three phenolic groups or those having three or more than three carboxylic acid groups. Branching agents which are suitable according to the invention are, for example, phloroglucinol, 4,6-dimethyl-2,4,6-tri-(4-hydroxyphenyl)-hept-2-ene, 4,6-dimethyl- 2,4,6-tri-(4-hydroxyphenyl)-heptane, 1,3,5-tri-(4-hydroxyphenyl)-benzene, 1,1,1- tris-(4-hydroxyphenyl)-ethane, tri-(4-hydroxyphenyl)-phenyl-methane, 2,2-bis-[4,4- bis-(4-hydroxyphenyl)-cyclohexyl]-propane, 2,4-bis-(4-hydroxyphenyl-isopropyl)- phenol, 2,6-bis-(2-hydroxy-5'-methyl-benzyl)-4-methylphenol, 2-(4- hydroxyphenyl)-2-(2,4-dihydroxyphenyl)-propane, hexa-(4-(4-hydroxyphenyl- isopropyl)-phenyl) terephthalate, tetra-(4-hydroxyphenyl)-methane, tetra-(4-(4- hydroxyphenyl-isopropyl)-phenoxy)-methane and l,4-bis-(4',4"- dihydroxytriphenyl)-methylbenzene and 2,4-dihydroxybenzoic acid, trimesic acid, cyanuric chloride, 3,3-bis-(3-methyl-4-hydroxyphenyl)-2-oxo-2,3-dihydroindole, trimesic acid trichloride and o,a',Q!"-tris-(4-hydroxyphenyl)-l,3,5-triisopropylbenzene.Branching agents which are preferably to be employed are l,l,l-tris-(4-hydroxyphenyl)-ethane and 3,3-bis-(3-methyl-4-hydroxyphenyl)-2-oxo-2,3-dihydroindole. The amount of the branching agents optionally to be employed is preferably 0.05 mol% to 2 mol%, based on the moles of bisphenols employed. In the case of preparation of the polycarbonate by the phase boundary process, for example, the branching agents can be initially introduced into the aqueous alkaline phase with the bisphenols and the chain terminators, or they can be added as a solution in an organic solvent, together with the carbonic acid derivatives. In the case of the transesterification process, the branching agents are preferably metered in together with the dihydroxyaromatics or bisphenols. Catalysts which are preferably to be employed in the preparation of polycarbonate by the melt transesterification process are the ammonium salts and phosphonium salts known from the literature. Copolycarbonates can also be used according to the invention. Copolycarbonates in the context of the invention are, in particular, polydiorganosiloxane/polycarbonate block copolymers, the weight-average molecular weight (M w) of which is preferably 10,000 to 200,000 g/mol, particularly preferably 20,000 to 80,000 g/mol (determined by gel permeation chromatography after prior calibration by light scattering measurement or ultracentrifugation). The content of aromatic carbonate structural units in the polydiorganosiloxane/polycarbonate block copolymers is preferably 75 to 97.5 wt.%, particularly preferably 85 to 97 wt.%. The content of polydiorganosiloxane structural units in the polydiorganosiloxane/polycarbonate block copolymers is preferably 25 to 2.5 wt.%, particularly preferably 15 to 3 wt.%. The polydiorganosiloxane/polycarbonate block copolymers can be prepared, for example, starting from polydiorganosiloxanes containingα,ώ-bishydroxyaryloxy end groups and having an average degree of polymerization of preferably Pn = 5 to 100, particularly preferably Pn = 20 to 80. The polydiorganosiloxane/polycarbonate block polymers can also be a mixture of polydiorganosiloxane/polycarbonate block copolymers -with conventional polydiorganosiloxane structural units in this mixture preferably being 2.5 to 25 wt.%. Such polydiorganosiloxane/polycarbonate block copolymers are characterized in that they contain in the polymer chain on the one hand aromatic carbonate structural units (I) and on the other hand polydiorganosiloxanes (2) containing aryloxy end groups (Figure Removed) are identical or different difunctional aromatic radicals and R and R1 are identical or different and denote linear alkyl, branched alkyl, alkenyl, halogenated linear alkyl, halogenated branched alkyl, aryl or halogenated aryl, preferably methyl, and denotes the average degree of polymerization of preferably 5 to 100, particularly preferably 20 to 80. Alkyl in the above formula (2) is preferably Ci-C2o-alkyl, alkenyl in the above formula (2) is preferably C2-C6-alkenyl; aryl in the above formulae (1) and (2) is preferably C6-C14-aryl. Halogenated in the above formula means partly or completely chlorinated, brominated or fluorinated. Examples of alkyls, alkenyls, aryls, halogenated alkyls and halogenated aryls are methyl, ethyl, propyl, n-butyl, tert-butyl, vinyl, phenyl, naphthyl, chloromethyl, perfluorobutyl, perfluorooctyl and chlorophenyl. Such polydiorganosiloxane/polycarbonate block copolymers and their preparation belong to the prior art. Preferred polydiorganosiloxane/polycarbonate block copolymers can be prepared e.g. by reacting polydiorganosiloxanes containing α,ώ-bishydroxyaryloxy end groups together with other bisphenols, optionally with the co-use of branching agents in the conventional amounts, e.g. by the two-phase boundary process (as described, for example, in H. Schnell, "Chemistry and Physics of Polycarbonates", Polymer Reviews, volume 9, p. 31-76, Interscience Publishers, New York, London, Sydney, 1964). The polydiorganosiloxanes containing o,oo-bishydroxyaryloxy end group used as educts for this synthesis and their preparation are described, for example, in US-A 3419 634. Conventional additives, such as e.g. mould release agents, can be admixed to the polycarbonates in the melt or applied to the surface. The polycarbonates to be used preferably already comprise mould release agents before compounding with the other components of the moulding compositions according to the invention. According to the invention, a graft polymer or a mixture of two or more graft copolymers which are obtained by grafting polymerization of at least one vinyl monomer on to a graft base based on olefinically unsaturated olefin polymers or olefinically unsaturated olefin copolymers are employed as component C). According to the invention, graft polymers of Cl) 5 to 95 wt.%, preferably 10 to 80 wt.%, in particular 20 to 50 wt.% of at least one vinyl monomer on C2) 95 to 5 wt.%, preferably 90 to 20, in particular 80 to 20 wt.% of one or more graft bases having glass transitions temperatures of the rubber component of are employed as component C). The graft base C2) in general has an average particle size (d50 value) of 0.05 to 5 μm, preferably 0.10 to 2 μm, particularly preferably 0.15 to 1 μm. Monomers Cl) are preferably mixtures Cl.l) of 50 to 99 parts by wt., preferably 60 to 80 parts by wt. of vinylaromatics and/or vinylaromatics substituted on the nucleus, such as styrene, a-methylstyrene, p-methylstyrene or p-chlorostyrene, and/or acrylic acid (C1-C8)-alkyl esters and/or methacrylic acid (Ci-Cg)-alkyl esters, such as methyl methacrylate and ethyl methacrylate, and C1.2) 1 to 50 parts by wt., preferably 40 to 20 parts by wt. of vinyl cyanides (unsaturated nitriles, such as acrylonitrile and methacrylonitrile) and/or (meth)acrylic acid (C1-C8)-alkyl esters, such as methyl methacrylate, n-butyl acrylate and t-butyl acrylate, and/or derivatives, such as anhydrides and imides, of unsaturated carboxylic acids, for example maleic anhydride and N-phenylmaleimide. Particularly preferred monomers Cl. 1) are chosen from at least one of the monomers styrene, a-methylstyrene and methyl methacrylate, and particularly preferred monomers C1.2) are chosen from at least one of the monomers acrylonitrile, maleic anhydride and methyl methacrylate. Particularly preferred monomers are Cl.l styrene and C1.2 acrylonitrile and Cl.l styrene and C1.2 methyl methacrylate. Preferred graft bases C2 are diene rubbers (e.g. based on butadiene, isoprene etc.) or mixtures of diene rubbers or copolymers of diene rubbers or mixtures thereof with further copolymerizable monomers (e.g. according to Cl.l and C1.2), with the proviso that the glass transition temperature of component C2 is below preferably Pure polybutadiene rubber is particularly preferably employed. Particularly preferred polymers C are e.g. ABS polymers (emulsion, bulk and suspension ABS) such as are known to the expert from the literature, for example from Ullmann, Enzyklopadie der Technischen Chemie, vol. 19 (1980), p. 280 et seq. The gel content of the graft base C2 is at least 30 wt.%, preferably at least 40 wt.% (measured in toluene). The graft copolymers C) are prepared by free-radical polymerization, e.g. by emulsion, suspension, solution or bulk polymerization, preferably by emulsion or bulk polymerization. ABS polymers which are prepared by redox initiation with an initiator system of organic hydroperoxide and ascorbic acid in accordance with US-A 4 937 285 are also particularly suitable graft rubbers. Since as is known in the grafting reaction the grafting monomers are not necessarily completely grafted on to the graft base, according to the invention graft polymers C) are also understood as meaning those products which are obtained by (co)polymerization of the grafting monomers in the presence of the graft base and are co-obtained during the working up. Products known to the expert as MBS rubbers, such as e.g. are marketed by Rohm und Haas under the name Paraloid® EXL 2600, Paraloid EXL 2650 or Paraloid® EXL 2691 and which are described e.g. in EP-A 0 985 682, are particularly preferred as polymers C). According to the invention, one or a mixture of two or more graft copolymers which are obtained by grafting polymerization of at least one vinyl monomer on to a graft base based on rubber-elastic acrylate polymers or on rubber-elastic acrylate copolymers are employed as component D). According to the invention, graft polymers of Dl) 5 to 95 wt.%, preferably 10 to 80 wt.%, in particular 20 to 50 wt.% of at least one vinyl monomer on D2) 95 to 5 wt.%, preferably 90 to 20, in particular 80 to 20 wt.% of one or more graft bases having glass transitions temperatures of the rubber component of are employed as component D). The graft base D2) in general has an average particle size (djo value) of 0.05 to 5 fan, preferably 0.10 to 2 /mi, particularly preferably 0.15 to 1 μm. Monomers Dl) are preferably mixtures Dl.l) of 50 to 99, preferably 60 to 80 parts by wt. of vinylaromatics and/or vinylaromatics substituted on the nucleus, such as styrene, a-methylstyrene, p-methylstyrene or p-chlorostyrene, and/or acrylic acid (Ci-Cg)-alkyl esters and/or methacrylic acid (Ci-C8)-alkyl esters, such as methyl methacrylate and ethyl methacrylate, and D1.2) 1 to 50, preferably 40 to 20 parts by wt. of vinyl cyanides (unsaturated nitriles, such as acrylonitrile and methacrylonitrile) and/or (meth)acrylic acid (C1-C8)-alkyl esters, such as methyl methacrylate, n-butyl acrylate and t-butyl acrylate, and/or derivatives, such as anhydrides and imides, of unsaturated carboxylic acids, for example maleic anhydride and N-phenylmaleimide. Particularly preferred monomers Dl.l) are chosen from at least one of the monomers styrene, a-methylstyrene and methyl methacrylate, and particularly preferred monomers D1.2) are chosen from at least one of the monomers acrylonitrile, maleic anhydride and methyl methacrylate. Particularly preferred monomers are Dl.l styrene and D1.2 acrylonitrile. Suitable acrylate rubbers according to D2 of the polymers D are, preferably, polymers of acrylic acid alkyl esters, optionally with up to 40 wt.%, based on D2, of other polymerizable, ethylenically unsaturated monomers. Preferred polymerizable acrylic acid esters include C1-C8-alkyl esters, for example the methyl, ethyl, butyl, n-octyl and 2-ethylhexyl ester, halogenoalkyl esters, preferably halogeno-C1-C8-alkyl esters, such as chloroethyl acrylate, and mixtures of these monomers. For crosslinking, monomers having more than one polymerizable double bond can be copolymerized. Preferred examples of crosslinking monomers are esters of unsaturated monocarboxylic acids having 3 to 8 C atoms and unsaturated monohydric alcohols having 3 to 12 C atoms, or saturated polyols having 2 to 4 OH groups and 2 to 20 C atoms, such as e.g. ethylene glycol dimethacrylate and allyl methacrylate; polyunsaturated heterocyclic compounds, such as e.g. trivinyl and triallyl cyanurate; polyfunctional vinyl compounds, such as di- and trivinylbenzenes, dicyclopentadiene and 5-ethylidenenorbornene; and also triallyl phosphate and diallyl phthalate. Preferred crosslinking monomers are allyl methacrylate, ethylene glycol dimethacrylate, diallyl phthalate and heterocyclic compounds which have at least 3 ethylenically unsaturated groups. Particularly preferred crosslinking monomers are the cyclic monomers triallyl cyanurate, triallyl isocyanurate, triacryloylhexahydro-s-triazine and triallylbenzenes. The amount of the crosslinked monomers is preferably 0.02 to 5, in particular 0.05 to 2 wt.%, based on the graft base D2. In the case of cyclic crosslinking monomers having at least 3 ethylenically unsaturated groups, it is advantageous to limit the amount to below 1 wt.% of the graft base D2. Preferred "other" polymerizable, ethylenically unsaturated monomers which can optionally be used for the preparation of the graft base D2, in addition to the acrylic acid esters, are e.g. acrylonitrile, styrene, a-methylstyrene, acrylamides, vinyl C1-C6-alkyl ethers and methyl methacrylate. Preferred acrylate rubbers as the graft base D2 are emulsion polymers which have a gel content of at least 60 wt.%. The preparation of the graft base D2 can be carried out in one step or in several steps. A mixture of various graft bases according to the description can also be employed for the grafting reaction. In particular, various graft bases which differ in average particle size can also be employed. ASA rubbers such as are described e.g. in WO 2000046296, in EP 0960145 or in DE 4229913 are particularly preferred as component D) according to the invention. The compositions according to the invention comprise as component E) known UV stabilizers, such as are described, for example, in Gachter, Mtiller, Kunststoff-Additive, 3rd edition, Hanser-Verlag, Munich, Vienna, 1989 and in the Plastics Additives Handbook, 5th edition, Hanser-Verlag, Munich, 2001, p. 97-137, 141-154, 178-183, 188-192, 369-372 and 389-394. The UV stabilizers can be employed by themselves or in a mixture or in the form of masterbatches. Preferred UV stabilizers which are to be employed according to the invention are sterically hindered phenols, sterically hindered amines (HALS = hindered amine light stabilizer), hydroquinones, aromatic secondary amines, such as diphenylamines, substituted resorcinols, salicylates, benzotriazoles and benzophenones, and variously substituted representatives of these groups and mixtures thereof. Sterically hindered amines of the HALS type, benzotriazoles, benzotriazines and benzopyrimidines are particularly preferred. The sterically hindered amines of the HALS type which are preferably to be employed can be derived from the general structure shown in (3) (Figure Removed) In this formula, the radicals can be, in each case independently of one another: Y: H, acyl, O radical, alkyl, alkenyl, alkoxyalkyl, arylalkyl, X2: -OR, NR2, maleimide, 7 o R and R independently of one another = H, alkyl, alkenyl, arylalkyl, preferably = H R3, R4, R5, R6 independently of one another H, alkyl, phenyl, alkylaryl, aromatic heterocyclic radical containing oxygen, sulfur or nitrogen; preferably R3-R6 are methyl The HALS stabilizers which are preferably to be employed are described, for example, in US 4895901, US 4210612 and US 5015682. The benzotriazoles which are preferably to be employed can be derived generally from the structure shown in (4). (Figure Removed) In this formula, R9 and R10 can be chosen independently of one another from the group consisting of H, alkyl (in particular methyl, ethyl, propyl), cycloalkyl, halogen, haloalkyl, alkoxy, alkylene, aryl, alkyl-aryl or a combination of these. Particularly preferably, R9 = R10 = (2-phenyl)-isopropyl, R9 = H and R10 = 2-(2,4,4-trimethyl)-pentyl, R9 = H and R10= methyl, R9 = R10 = t-butyl, R9 = t-butyl and R10 = methyl, R9 = R10 = 2-(2-methyl)-butyl, R9 = iso-butyl and R10 = 2-(2,4,4-trimethyl)-pentyl. The benzotriazoles described which are preferably to be employed according to the invention are marketed, for example, by Ciba Spezialchemikalien, Basle, Switzerland under the commercial product name Tinuvin®. The hydroxyphenyltriazine and -pyrimidine UV stabilizers which are preferably to be employed consist of two phenyl groups and one resorcinol group, which are bonded to a triazine or pyrimidine ring, as described in US 6 239 276 and US 5 597 854. The hydroxyphenyltriazines and -pyrimidines which are preferably to be employed can be derived generally from the general structure shown in (5). In formula (5), A can be N or CH and R to R independently of one another can be chosen from the group consisting of H, alkyl (in particular methyl, ethyl, propyl), cycloalkyl, halogen, haloalkyl, alkoxy, alkylene, aryl, alkyl-aryl or combinations of these. Examples of commercially available representatives of the hydroxyphenyltriazines which are preferably to be employed are Tinuvin® 1577 (CAS number 147315-50-2, Ciba Spezialchemikalien, Basle, Switzerland) or Cyasorb® UV 1164 (Cyctec Industries). The compositions according to the invention comprise as component F) conventional colouring agents and/or pigments, such as e.g. titanium dioxide, ultramarine blue, iron oxide, carbon black, phthalocyanines, quinacridones, perylenes, nigrosin and anthraquinones and derivatives thereof. The colouring agents described in US-A 6 476 158 are also suitable, in particular, for improving the gloss after weathering. The colouring agents and/or pigments can be added as the substance or as a masterbatch, for example in component A), component B), component C), polyethylene, polypropylene, waxes or paraffin. The colouring agents to be employed according to the invention are also described, for example, in Plastics Additives Handbook, 5th edition, Hanser-Verlag, Munich, 2001, p. 822-850. According to the invention, the compositions can comprise as component G) at least difunctional, low molecular weight and oligomeric compounds which have at least one epoxide group. Preferred epoxide-containing compounds as component G are, generally: 1. Polyglycidyl or poly-(jS-rnethylglycidyl) ethers obtainable by reaction of a compound having at least two free alcoholic or phenolic hydroxyl groups and/or phenolic hydroxyl groups and a suitably substituted epichlorohydrin under alkaline conditions, or in the presence of an acidic catalyst with subsequent treatment with alkali. Ethers of this type are derived, for example, from acyclic alcohols, such as ethylene glycol, diethylene glycol and higher poly-(oxyethylene) glycols, propane-1,2-diol or poly-(oxypropylene) glycols, propane-1,3-diol, butane-1,4-diol, poly-(oxytetramethylene) glycols, pentane-1,5-diol, hexane-l,6-diol, hexane-2,4,6-triol, glycerol, 1,1,1-trimemylolpropane, bistrimethylolpropane, pentaerymritol and sorbitol, and from polyepichlorohydrins. However, they are also derived, for example, from cycloaliphatic alcohols, such as 1,3- or 1,4-dihydroxycyclohexane, bis-(4-hydroxycyclohexyl)-methane, 2,2-bis-(4-hydroxycyclohexyl)-propane or l,l-bis-(hydroxymethyl)-cyclohex-3-ene, or they have aromatic nuclei, such as N,N-bis-(2-hydroxyethyl)-aniline or p,p'-bis-(2-hydroxyethyl-amino)-diphenylmethane. The epoxide compounds can also be derived from mononuclear phenols, such as, for example, from resorcinol or hydroquinone; or they are based on polynuclear phenols, such as, for example, on bis-(4-hydroxyphenyl)-methane, 2,2-bis-(4-hydroxyphenyl)-propane, 2,2-bis-(3,5-dibromo-4-hydroxyphenyl)-propane or 4,4'-dihydroxydiphenyl sulfone, or on condensation products of phenols with formaldehyde which are obtained under acidic conditions, such as phenol-novolaks. 2. Difunctional, cycloaliphatic epoxide-containing compounds which contain the structural fragment shown in (6) (Figure Removed) In formula (6), R in each case independently of one another can be chosen from the group consisting of H, alkyl, aryl, halogen, halogenoalkyl, alkoxy, carboalkoxy and carbonyl, and n can be chosen from 0 to 8, preferably 0 to 2. Preferred examples from the class of cycloaliphatic epoxide-containing compounds which can optionally be employed according to the invention are 3,4- epoxycyclohexyl 3,4-epoxycyclohexylcarboxylate (commercial product ERL 4221 from Union Carbide), bis-(3,4-epoxycyclohexylmethyl) adipate, vinylcyclohexene diepoxide, 3,4-epoxy-6-methyl-cyclohexylmethyl 3',4'-epoxy-6'- methylcyclohexanecarboxylate, 2,3-epoxycyclohexyl 3,4- epoxycyclohexylcarboxylate, 4-(3,4-epoxy-5-methylcyclohexyl)-butyl 3',4'-epoxycyclohexylcarboxylate and 3,4-epoxy-cyclohexyl-ethylene oxide. 3. Poly-(N-glycidyl) compounds obtainable by dehydrochlorination of the reaction products of epichlorohydrin with amines. These amines are, for example, aniline, toluidine, n-butylamine, bis-(4-aminophenyl)-methane, m-xylylenediamine or bis-(4-methylaminophenyl)-methane, but also N,N,0-triglycidyl-m-aminophenol or N,N,O-triglycidyl-p-aminophenol. The poly-(N-glycidyl) compounds also include, however, N,N'-diglycidyl derivatives of cycloalkylene-ureas, such as ethylene-urea or 1,3-propylene-urea, and N,N'-diglycidyl derivatives of hydantoins, such as of 5,5-dimethylhydantoin. Nitrogen compounds which can preferably be employed are also nitrogen-containing heterocyclic compounds, such as triazines, barbituric acids, hydantoins, uracils, pyromellitic acid diimides, piperidines, piperazines, piperazinediones and isocyanurates. The thermoplastic moulding compositions can comprise as component H) a filler or reinforcing substance or a mixture of two or more different fillers and/or reinforcing substances, for example based on talc, mica, silicate, quartz, titanium dioxide, wollastonite, kaolin, amorphous silicas, magnesium carbonate, chalk, feldspar, barium sulfate and glass beads, and/or fibrous fillers and/or reinforcing substances based on carbon fibres and/or glass fibres. Mineral particulate fillers based on talc, mica, silicate, quartz, titanium dioxide, wollastonite, kaolin, amorphous silicas, magnesium carbonate, chalk, feldspar, barium sulfate and/or glass fibres are preferably employed. According to the invention, mineral particulate fillers based on talc, wollastonite and/or glass fibres are particularly preferred. Fillers based on talc are most preferred. For uses in particular in which isotropy in the dimensional stability and a high thermal dimensional stability is required, such as, for example, in motor vehicle uses for vehicle body exterior components, mineral fillers are preferably employed, particularly preferably talc, wollastonite or kaolin. Needle-shaped mineral fillers are also particularly preferred. According to the invention, needle-shaped mineral fillers are understood as meaning a mineral filler with a highly pronounced needle-shaped character. Needle-shaped wollastonites may be mentioned as an example. The mineral preferably has a length : diameter ratio of 2:1 to 35:1, particularly preferably 3:1 to 19:1, most preferably 4:1 to 12:1.The average particle size of the needle-shaped minerals according to the invention is preferably less than 20 μm, particularly preferably less than 15 μm, especially preferably less than 10 μm, most preferably less than 5 μm, determined with a CILAS GRANULOMETER. Mineral fillers based on talc are most preferred as component H). In the context of the invention, possible mineral fillers based on talc are all the particulate fillers which the expert associates with talc or talcum. All the particulate fillers which are commercially available and have product descriptions which contain the terms talc or talcum as characterizing features are also possible. Mineral fillers which have a content of talc according to DIN 55920 of greater than 50 wt.%, preferably greater than 80 wt.%, particularly preferably greater than 95 wt.% and especially preferably greater than 98 wt.%, based on the total weight of filler, are preferred. The mineral fillers based on talc can also be treated on the surface. For example, they can be finished with an adhesion promoter system e.g. based on silane. The mineral fillers to be employed according to the invention which are based on talk preferably have an upper particle or grain size d97 of less than 50 μm, preferably less than 10 μm, particularly preferably less than 6μm and especially preferably less than 2.5 μm. The average particle size d50 chosen is preferably a value of less than 10 μrn, preferably less than 6 μm, particularly preferably less than 2 /an and especially preferably less than 1 μm. The d97 and d50 values of the fillers are determined by SEDIGRAPH D 5 000 sedimentation analysis or by DIN 66 165 sieve analysis. The average aspect ratio (diameter to thickness) of the particulate fillers based on talc is preferably in the range from 1 to 100, particularly preferably 2 to 25 and especially preferably 5 to 25, determined on electron microscopy photographs ofultra-thin sections of the finished products and by measurement of a representative amount (approx. 50) of filler particles. The filler and/or reinforcing substance can optionally be modified on the surface, for example with an adhesion promoter or adhesion promoter system, e.g. based on silane. However, the pretreatment is not absolutely necessary. In particular, if glass fibres are used polymer dispersions, film-forming agents, branching agents and/or glass fibre processing auxiliaries can also be used in addition to silanes. According to the invention, glass fibres which in general have a fibre diameter of between 7 and 18 μm, preferably between 9 and 15 μm, can also be particularly preferably employed. These can be added as continuous fibres or as cut or ground glass fibres, it being possible for the fibres to be finished with a suitable size system and an adhesion promoter or adhesion promoter system, e.g. based on silane. Customary silane compounds for pretreatment with a size system have, for example, the general formula in which the substituents have the following meaning: (Figure Removed) q an integer from 2 to 10, preferably 3 to 4 r an integer from 1 to 5, preferably 1 to 2 k an integer from 1 to 3, preferably 1. Preferred silane compounds are aminopropyltrimethoxysilane, aminobutyltrimethoxysilane, aminopropyltriethoxysilane, aminobutyltriethoxysilane and the corresponding silanes which contain a glycidyl group as the substituent X. The silane compounds can in general be employed for the surface coating in amounts of 0.05 to 2 wt.%, preferably 0.5 to 1.5 wt.% and in particular 0.8 to 1 wt.%, based on the mineral filler. Due to the processing to give the moulding composition or shaped article, the particulate fillers can have a lower d97 or d50 value in the moulding composition or in the shaped article than the fillers originally employed. Due to the processing to give the moulding composition or shaped article, the glass fibres can have shorter length distributions in the moulding composition or in the shaped article than originally employed. The particle diameter in the finished product can be determined here, for example, by recording electron microscopy photographs of thin sections of the polymer mixture and using at least 25, preferably at least 50 filler particles for the evaluation. The compositions according to the invention can furthermore comprise as component I) conventional additives, which in general can be added in amount of up to 15 wt.%, preferably in an amount of 0.01 to 10 wt.%, particularly preferably 0.05 to 5 wt.%, especially preferably 0.1 to 3 wt.%, based on the total weight of the moulding compositions. All the conventional additives, such as e.g. stabilizers (for example heat stabilizers), antistatics, flow agents, mould release agents, fireproofing additives, emulsifiers, nucleating agents, plasticizers, lubricants, additives which lower the pH (e.g. compounds containing carboxyl groups) and additives for increasing the conductivity can be possible here. The additives mentioned and further suitable additives are described, for example, in Gachter, Miiller, Kunststoff-Additive, 3rdedition, Hanser-Verlag, Munich, Vienna, 1989. The additives can be employed by themselves or as a mixture or in the form of masterbatches. The additives can be admixed and/or applied to the surface. Stabilizers which can be employed are, for example, sterically hindered phenols and/or phosphites, hydroquinones, aromatic secondary amines, such as diphenylamines, substituted resorcinols, salicylates, benzotriazoles and benzophenones, and variously substituted representatives of these groups and mixtures thereof. Nucleating agents which can be employed are e.g. sodium phenyl phosphinate, aluminium oxide, silicon dioxide and, preferably talc and the nucleating agents described above. Lubricants and mould release agents which can be employed are ester waxes, pentaerithrityl stearate (PETS), long-chain fatty acids (e.g. stearic acid or behenic acid), their salts (e.g. Ca or Zn stearate) and amide derivatives (e.g. ethylene-bis-stearylamide) or montan waxes (mixtures of straight-chain, saturated carboxylic acids having chain lengths of 28 to 32 C atoms) and low molecular weight polyethylene or polypropylene waxes. Plasticizers which can be employed are, for example, phthalic acid dioctyl ester, phthalic acid dibenzyl ester, phthalic acid butyl benzyl ester, hydrocarbon oils and N-(n-butyl)benzenesulfonamide. In order to obtain conductive moulding compositions, carbon blacks, conductivity blacks, carbon fibrils, nanoscale graphite fibres (nanotubes), graphite, conductive polymers, metal fibres and other conventional additives for increasing the conductivity can be added. Flameproofing agents which can be employed are commercially available organic halogen compounds with synergists or commercially available organic nitrogen compounds or organic/inorganic phosphorus compounds, individually or in a mixture. Mineral flameproofing additives, such as magnesium hydroxide or Ca/Mg carbonate hydrates (e.g. DE-A 4 236 122) can also be employed. Examples of halogen-containing, in particular brominated and chlorinated compounds which may be mentioned are: ethylene-l,2-bistetrabromophthalimide, epoxidized tetrabromobisphenol A resin, tetrabromobisphenol A oligocarbonate, tetrachlorobisphenol A oligocarbonate, pentabromopolyacrylate and brominated polystyrene. Suitable organic phosphorus compounds are the phosphorus compounds according to WO-A 98/17720, e.g. triphenyl phosphate (TPP), resorcinol bis-(diphenyl phosphate), including oligomers, and bisphenol A bis-diphenyl phosphate, including oligomers (cf. e.g. EP-A 0 363 608 and EP-A 0 640 655), melamine phosphate, melamine pyrophosphate, melamine polyphosphate and mixtures thereof. Possible nitrogen compounds are, in particular, melamine and melamine cyanurate. Suitable synergists are e.g. antimony compounds, in particular antimony trioxide and antimony pentoxide, zinc compounds, tin compounds, such as e.g. tin stannate, and borates. Carbon-forming agents and tetrafluoroethylene polymers can be added. The flameproofing agents, optionally with a synergist, such as antimony compounds, and antidripping agents, are in general employed in an amount of up to 30 wt.%, preferably 20 wt.% (based on the total composition). Reinforcing substances, e.g. in the form of glass fibres, can also be added as additives. The invention furthermore provides a process for the preparation of the compositions, the use of the composition according to the invention for the production of semi-finished products and mouldings and semi-finished products and mouldings produced therefrom. The compositions according to the invention are prepared by known processes by mixing the components. It may be advantageous to premix individual components. The premixing can take place here both as a dry blend and by joint kneading, extrusion or milling of the components. Mixing in of individual components, in particular stabilizers, additives and colouring agents, can furthermore already be carried out during synthesis of the polymers employed according to the invention. Mixing of components A to D and further constituents is preferably effected at temperatures of 220 to 330 °C by joint kneading, extrusion or milling of the components. The compositions according to the invention can be processed to all types of semifinished products or moulding by conventional processes. Examples of processing processes which may be mentioned are extrusion processes and injection moulding processes. Examples of semi-finished products which may be mentioned are films and sheets. Because of the high colour homogeneity, the mouldings are particularly suitable for uses which are visually and optically important. According to the invention, the mouldings can be employed in a non-lacquered form or in a form coated with a transparent clear lacquer system. However, the mouldings can of course also be lacquered with a colouring base lacquer. The mouldings can be small or large components and can be employed for exterior or interior uses. Preferably, large-component mouldings are produced for vehicle construction, in particular the automobile sector. In particular, vehicle body exterior components, such as e.g. mud guards, tail gates, engine bonnets, bumpers, loading areas, covers for loading areas, car roofs, air intake grills, spoilers or other vehicle body components, can be produced from the moulding compositions according to the invention. Mouldings or semi-finished products from the moulding compositions/compositions according to the invention can also be in a composite with further materials, such as e.g. metal or plastic. The moulding compositions according to the invention or themouldings/semi-finished products from the moulding compositions according to the invention can be employed in a composite with other materials or with themselves for the production of finished components, such as e.g. vehicle body exterior components, by conventional techniques of bonding and joining of several components or parts, such as e.g. coextrusion, injection moulding under films, injection moulding around embedded components, gluing, welding, screwing or clamping. The moulding compositions according to the invention can also be used for numerous further uses. Examples which may be mentioned are the use in electrical and electronics engineering and in the construction sector. Mouldings from the moulding compositions according to the invention can be used in the fields of use mentioned, for example, as lamp covers, as safety panes, as housing material for electronic apparatuses, as housing material for domestic appliances and as sheets for the production of covers. The compositions according to the invention are distinguished by a very good colour homogeneity and by a very good stability to weathering. They moreover fulfil high requirements with regard to processing stability, flowability of the melt, toughness, toughness at low temperatures, rigidity, heat distortion point, thermal expansion, surface quality, lacquerability, resistance to chemicals and resistance to fuels. Examples Component A Polybutylene terephthalate type Al: Component A is polybutylene terephthalate having an intrinsic viscosity IV of 0.93 cm3/g, commercial product Pocan® B1300 from Bayer AG, Leverkusen. The intrinsic viscosity is measured in phenol/o-dichlorobenzene (1:1 parts by wt.) at 25 °C. Component B Polycarbonate type Bl: Linear polycarbonate (Makrolon® 2405 from Bayer AG, Leverkusen, Germany) based on bisphenol A having a viscosity )?rel. of approx. 1.29 (measurement conditions: 5 g polycarbonate per litre of methylene chloride, 25 °C) and a molecular weight Mw of approx. 29,000 g/mol (determined with GPC methods against a polycarbonate standard). Component Cl Component Cl is Paraloid® EXL 2650 from Rohm und Haas Deutschland GmbH, Frankfurt. Component C2 Component C2 is a graft copolymer of acrylonitrile and styrene on a graft base of polybutadiene, intermediate product of Bayer AG, Leverkusen having a polybutadiene content of 75 wt.% and a styrene content in the shell of 28 wt.%. Comparison component VI Comparison component VI is the AES rubber Royaltuf® 970 E (former name Blendex® WX 270) from Crompton Corporation, Crompton GmbH Deutschland, Bergkamen. Component Dl Component Dl is a graft copolymer of acrylonitrile and styrene on a graft base of partly crosslinked polybutyl acrylate, Centrex® 57 WBA, intermediate product of Bayer Corp., Pittsburgh. Component D2 Component D2 is Paraloid® EXL 3361 (a core/shell impact modifier based on a partly crosslinked acrylate core) from Rohm & Haas Deutschland, Frankfurt. Component E Component E is Tinuvin® 350 from Ciba Geigy, Basle. Component F Component F is carbon black, type Black Pearls® 800 from Cabot GmbH, Hanau. Component G Component G is Araldit® GT 7071 (hydrolysis stabilizer based on a phenol/epichlorohydrin reaction product) from Huntsman Advanced Materials Deutschland GmbH, Bergkamen. In addition, commercially available processing auxiliaries are employed as additives. Compounding operations were carried out on a twin-screw extruder of the type ZSK32 (Werner und Pfleiderer) at melt temperatures of 250 to 290 °C. The test specimens were injection moulded on an injection moulding machine of the type Arburg 320-210-500 at melt temperatures of 260 to 280 °C and mould temperatures of 70 to 90 °C. The moulding compositions according to the invention were tested by the following methods: Vicat B: Heat distortion stability or heat distortion point in accordance with DIN ISO 306/B 120 in silicone oil. Izod impact strength: Toughness in accordance with ISO 180 method 1 U at -30 °C. Izod notched impact strength: Toughness in accordance with ISO 180 method 1 A at 23 °C. Tensile E modulus and tensile strength in accordance with DIN / EN / ISO 527-2/1 A. MVR: Flowability in accordance with DIN/ISO 1133 at 260 °C and 5 kg. Colour homogeneity: Determination of the colour homogeneity of the surface by visual assessment. "+" means a homogeneous coloration without the formation of stripes of lower colour intensity perpendicular to the direction of flow (tiger stripes)"0" means a largely homogenous coloration with slight formation of stripes of lower colour intensity perpendicular to the direction of flow "-" means an inhomogeneous coloration with severe formation of stripes perpendicular to the direction of flow. The evaluation of the colour homogeneity was carried out on sheets of 150 x 105 x 1.6 mm, which were produced with a melt temperature of 270 °C, a mould temperature of 80 °C and a filling rate of 50 mm/s via a film gate on a 105 mm side. As can be seen from table 1, the moulding compositions according to the invention have the required combination of very good colour homogeneity and good stability to hydrolysis (>60% of the initial tensile strength after hydrolysis) with simultaneously good mechanical properties. Compared with comparison examples 2 and 3, the moulding compositions according to the invention moreover are significantly more stable to UV, because the content of UV-sensitive components C is significantly lower. The composition and properties of the thermoplastic moulding compositions according to the invention can be seen from table 1. (Table Removed) We Claim: 1. Composition consisting of (A) 4 to 80 parts by wt. of a polyalkylene terephthalate, (B) 10 to 90 parts by wt. of a aromatic polycarbonate, (C) 1.5 to 30 parts by wt. of a graft polymer based on polybutadiene as the rubber component, (D) 1.5 to 30 parts by wt. of a graft polymer based on acrylates as the rubber component, (E) 0.01 to 5 parts by wt. of UV stabilizers of the kind such as herein described, (F) 0.01 to 10 parts by wt. of colouring agent of the kind such as herein described, (G) 0 to 5 parts by wt. of hydrolysis stabilizers of the kind such as herein described, (H) 0 to 54 parts by wt. of a particulate mineral filler of the kind such as herein described, (I) 0 to 10 parts by wt. of further additives of the kind such as herein described. 2. Composition as claimed in claim 1, wherein C) is composed of graft polymers of C1) 5 to 95 wt.% of at least one vinyl monomer on C2) 95 to 5 wt.% of one or more graft bases having glass transition temperatures of the rubber component of 3. Composition as claimed in claim 1 or 2, wherein C1) is a mixture of C1.1) 50 to 99 parts by wt. of styrene, α-methylstyrene, ß-methylstyrene, p-chlorostyrene and /or acrylic acid (C1-C8)-alkyl esters and/or methacrylic acid (C1-C8)-alkyl esters and C1.2) 1 to 50 parts by wt. of vinyl cyanides and/or (meth)acrylic acid (C1-C8)-alkyl esters and/or anhydrides and imides of unsaturated carboxylic acids. 4. Composition as claimed in claim 1 or 2, wherein D) is composed of graft polymer of D1) 5 to 95 wt.% of at least one vinyl monomer on D2) 95 to 5 wt.% of one or more graft bases having glass transition temperatures of the rubber component of 5. Compositions as claimed in one or more of the preceding claims, wherein polyethylene terephthalate is employed as component A. 6. The composition as claimed in claim 1 as and when used to prepare mouldings and semifinished products.

Full Text

The present invention relates to composition.
The present invention relates to coloured, weathering-stabilized compositions based on impact-modified polyalkylene terephthalate/polycarbonate blends and moulding compositions, semi-finished products and mouldings produced therefrom, whichrare employed, for example, for motor vehicle exterior uses in non-lacquered form or in a form coated only with a transparent clear lacquer.
Impact-modified moulding compositions which comprise partly crystalline polyesters, amorphous polycarbonates and graft copolymers are known. Such moulding compositions are employed, for example, in the automobile sector for mouldings such as bumpers, mud guards, radiator grills, headlamp screens, tailgate screens, sills, spoilers, door handles, tank caps, linings, horizontal structural components, such as engine bonnets or roof elements, door modules or the like. Prerequisites for use in motor vehicle applications are a high heat distortion point, high flowability in the melt, good lacquer adhesion, high resistance to chemicals, high rigidity, high dimensional stability and high toughness at low temperatures.
Mouldings of impact-modified polyalkylene terephthalate/polycarbonate blends can be coloured by two different methods. Traditionally, the mouldings are lacquered with a colouring lacquer, the so-called base lacquer. The mouldings can optionally moreover have been coated with primer and/or filler before the base lacquer. A transparent clear lacquer can furthermore optionally be applied to the base lacquer. These systems are called top-lacquered systems in the following. In top-lacquered systems the intrinsic colour of the moulding compositions is substantially irrelevant, since colouring is done by the base lacquer.
As an alternative to the top-lacquered systems, there are systems which are called moulded-in colour systems in the following. In moulded-in colour systems the colour of the moulding in use is determined by the intrinsic colour of the moulding
composition, that is to say moulded-in colour systems are not lacquered with a primer, filler or colouring base lacquer. However, the moulded-in colour systems can optionally be coated with transparent clear lacquer. The advantage of moulded-in colour systems lies in the saving in costs, since the working steps of priming with primer and/or fillers and of lacquering with colouring base lacquers and the associated drying operations are omitted.
The use of mouldings of impact-modified polyalkylene terephthalate/polycarbonate blends in the motor vehicle exterior sector involves high requirements in respect of the weathering resistance of the material of the mouldings. In this context, the resistance to photooxidation by UV irradiation (called UV stability in the following) and the resistance of the materials to hydrolysing environmental influences (called stability to hydrolysis in the following) are of central importance.
hi top-lacquered systems the harmful UV rays are largely kept back by the base lacquer. On the other hand, in moulded-in colour systems there is no UV-blocking function of a covering base lacquer. At best a UV-absorbing clear lacquer can hold off the majority of the harmful UV radiation in moulded-in colour systems. Nevertheless, moulding compositions which are based on moulded-in colour systems must have a high UV stability, and for this reason impact modifiers based on rubbers with conjugated dienes, such as, for example, butadiene in ABS or MBS rubbers, cannot be employed alone.
Weathering-stable PC/polyester blends therefore employ, for example, acrylate rubbers, as has been described in DE-A 33 02 124.
EP-B 0 787 769 describes the use of PC/polyester blends with a combination of AES and acrylate rubbers to obtain moulding compositions of improved stability to weathering and good toughness.

The stability to hydrolysis of impact-modified polyalkylene terephthalate/polycarbonate blends is required in particular if the mouldings of these materials are employed under conditions with a high outside temperature and high atmospheric humidity during the life of the motor vehicle.
US-A 5 354 791 describes the use of epoxide-substituted polyalkylene terephthalate moulding compositions in combination with metal-containing phosphorus compounds in impact-modified polyalkylene terephthalate/polycarbonate blends to improve the stability to hydrolysis. The improvement in the stability to hydrolysis is described here by the small change in the melt viscosity after storage of the material at 110 °C in water in an autoclave. The UV resistance and the nature of the surface are not the content of US-A 5 354 791.
In moulded-in colour systems, however, in addition to the stability to weathering the ability to be coloured homogeneously is also of very great importance. Precisely in the case of impact-modified PC/polyester blends with weathering-resistant acrylate impact modifiers, in the case of injection mouldings undesirable colour inhomogeneities occur, in which periodically recurring regions coloured less, which have an optically brighter effect, with more deeply coloured regions, which have an optically darker or more colour-intensive effect, are formed perpendicular to the direction of flow during the injection moulding operation, these also being called tiger stripes. For mouldings which are perceived visually by the user in the end use, such as, for example, the motor vehicle exterior skin - such as e.g. mud guards, bumpers, tailgates, headlamp screens, spoilers, air intake grills, engine bonnets, car roofs - motor vehicle interiors, electrical housings or electronics housings, these tiger stripe effects are unacceptable.
The object was to develop homogeneously coloured impact-modified polyalkylene terephthalate/polycarbonate moulding compositions of improved weathering resistance for uses in so-called moulded-in colour systems. Increased requirements in respect of homogeneous colouring of the moulding compositions or mouldings

are imposed on moulded-in colour systems, since the colouring of the moulding composition is responsible at the same time for the colour appearance of the finished moulding in use.
It has now been found, surprisingly, that moulding compositions based on polyalkylene terephthalate/polycarbonate achieve the object described if at least two different systems based on graft copolymer compositions based on acrylates on the one hand and based on butadiene on the other hand are employed as the impact modifier in combination with stabilizers for increasing the UV resistance and for improving the resistance to hydrolysis. The mouldings from the compositions according to the invention are distinguished by a homogeneous appearance and homogeneous colour impression of the surface and excellent stability to weathering. The moulding compositions according to the invention are moreover distinguished by a high heat distortion point, good flowability in the melt, good lacquer adhesion, high resistance to chemicals, high rigidity, high dimensional stability and high toughness at low temperatures.
The invention provides compositions comprising
A) 4 to 80 parts by wt, preferably 10 to 60 parts by wt., particularly preferably
12 to 50 parts by wt., in particular 19 to 40 parts by wt. of at least one
polyalkylene terephthalate, preferably a polyethylene terephthalate or a
polybutylene terephthalate, particularly preferably a polybutylene
terephthalate,
B) 10 to 90 parts by wt., preferably 20 to 80 parts by wt., particularly preferably
25 to 60 parts by wt., in particular 30 to 60 parts by wt. of at least one
aromatic polycarbonate,
C) 1.5 to 30 parts by wt., preferably 3 to 25 parts by wt., particularly preferably
4 to 20 parts by wt., in particular 5 to 15 parts by wt. of at least one graft

polymer based on rubber-elastic olefinically unsaturated olefin (co)polymers, preferably polybutadiene, as the rubber component,
D) 1.5 to 30 parts by wt., preferably 3 to 25 parts by wt., particularly preferably
4 to 20 parts by wt., in particular 5 to 15 parts by wt. of at least one graft
polymer based on acrylates as the rubber component,
E) 0.01 to 5 parts by wt., preferably 0.05 to 3 parts by wt., particularly
preferably 0.1 to 1 part by wt. of a UV stabilizer,
F) 0.01 to 10 parts by wt., preferably 0.05 to 6 parts by wt., particularly
preferably 0.1 to 3 parts by wt. of colouring agent,
G) 0 to 5 parts by wt., preferably 0.05 to 3 parts by wt., particularly preferably
0.1 to 2 parts by wt. of hydrolysis stabilizers, preferably based on epoxide
compounds,
H) 0 to 54 parts by wt., preferably 3 to 34 parts by wt., particularly preferably 6 to 25, in particular 8 to 21 parts by wt. of at least one particulate mineral filler,
I) 0 to 10 parts by wt., preferably 0.05 to 3 parts by wt., particularly preferably 0.1 to 0.9 part by wt. of further additives.
According to the invention, the compositions comprise as component A one or a mixture of two or more different polyalkylene terephthalates. Polyalkylene terephthalates in the context of the invention are polyalkylene terephthalates which are derived from terephthalic acid (or its reactive derivatives) and alkanediols, for example based on ethylene glycol, propylene glycol or butanediol. According to the invention, preferably polybutylene terephthalate, polytrimethylene terephthalate and/or polyethylene terephthalate, particularly preferably polybutylene terephthalate

and/or polyethylene terephthalate, most preferably polybutylene terephthalate are employed as component A.
Polyalkylene terephthalates in the context of the invention are reaction products of aromatic dicarboxylic acids or their reactive derivatives (e.g. dimethyl esters or anhydrides) and aliphatic, cycloaliphatic or araliphatic diols and mixtures of these reaction products.
Preferred polyalkylene terephthalates can be prepared from terephthalic acid (or its reactive derivatives) and aliphatic or cycloaliphatic diols having 2 to IOC atoms by known methods (Kunststoff-Handbuch, vol. VIII, p. 695 et seq., Karl-Hanser-Verlag, Munich 1973).
Preferred polyalkylene terephthalates contain at least 80 mol%, preferably 90 mol%, based on the dicarboxylic acid, of terephthalic acid radicals and at least 80 mol%, preferably at least 90 mol%, based on the diol component, of radicals of ethylene glycol and/or propane- 1,3-diol and/or butane-1,4-diol.
The preferred polyalkylene terephthalates can contain, in addition to terephthalic acid radicals, up to 20 mol% of radicals of other aromatic dicarboxylic acids having 8 to 14 C atoms or aliphatic dicarboxylic acids having 4 to 12 C atoms, such as radicals of phthalic "acid, isophthalic acid, naphthalene-2,6-dicarboxylic acid, 4,4'-diphenyldicarboxylic acid, succinic acid, adipic acid, sebacic acid, azelaic acid, cyclohexanediacetic acid or cyclohexanedicarboxylic acid.
The preferred polyalkylene terephthalates can contain, in addition to radicals of ethylene glycol or propane-1,3-diol or butane-1,4-diol, up to 20 mol% of other aliphatic diols having 3 to 12 C atoms or cycloaliphatic diols having 6 to 21 C atoms, e.g. radicals of propane-1,3-diol, 2-ethylpropane-1,3-diol, neopentylglycol, pentane-l,5-diol, hexane-l,6-diol, cyclohexane-1,4-dimethanol, 3-methylpentane-2,4-diol, 2-methylpentane-2,4-diol, 2,2,4-trimethylpentane-1,3-diol and -1,6-diol, 2-

ethylhexane-l,3-diol,2,2-diethylpropane-l,3-diol, hexane-2,5-diol, hydroxyethoxy)-benzene, 2,2-bis-(4-hydroxycyclohexyl)-propane, 2,4-dihydroxy-1,1,3,3-tetramethyl-cyclobutane, 2,2-bis-(3-/3-hydroxyethoxyphenyl)-propane and 2,2-bis-(4-hydroxypropoxyphenyl)-propane.The polyalkylene terephthalates can be branched by incorporation of relatively small amounts of 3- or 4-hydric alcohols or 3- or 4-basic carboxylic acids, such as are described e.g. in DE-A 19 00 270 and US-A 3 692 744. Examples of preferred branching agents are trimesic acid, trimellitic acid, trimethylolethane and -propane and pentaerythritol.
It is advisable to use not more than 1 mol% of the branching agent, based on the acid component.
Polyalkylene terephthalates which have been prepared solely from terephthalic acid and reactive derivatives thereof (e.g. dialkyl esters thereof) and ethylene glycol and/or propane-l,3-diol and/or butane-1,4-diol (polyethylene terephthalate and polybutylene terephthalate) and mixtures of these polyalkylene terephthalates are particularly preferred.
Copolyesters which are prepared from at least two of the abovementioned acid components and/or from at least two of the abovementioned alcohol components are also preferred polyalkylene terephthalates, and particularly preferred copolyesters are poly-(ethylene glycol/butane- 1,4-diol) terephthalates.
The polyalkylene terephthalates in general have an intrinsic viscosity of approx. 0.4 to 1.5, preferably 0.5 to 1.3, in each case measured in phenol/o-dichlorobenzene (1:1 parts by wt.) at 25 °C.
The polyalkylene terephthalates to be employed according to the invention can preferably also be employed in a mixture with other polyesters and/or further

polymers. Particularly preferably, mixtures of polyalkylene terephthalates with other polyesters, very particularly preferably mixtures of polybutylene terephthalate with polyethylene terephthalate are employed.
Conventional additives, such as e.g. mould release agents, stabilizers and/or flow agents, can be added to the mixtures in the melt or applied to the surface.
According to the invention, the compositions according to the invention comprise as component B a polycarbonate or a mixture of polycarbonates.
Preferred polycarbonates are those homopolycarbonates and copolycarbonates based on the bisphenols of the general formula (I)

(Formula Removed)
wherein Z is a divalent organic radical having 6 to 30 C atoms which contains one or more aromatic groups.
Bisphenols of the formula (la)

(Figure Removed)
represents a single bond, C1-C5-alkylene, C2-C5-alkylidene, C5-C6-cycloalkylidene, -O-, -SO-, -CO-, -S-, -SO2-, C6-C12-arylene, on to which further aromatic rings optionally containing heteroatoms can be fused,or a radical of the formula (II) or (III)
B represents in each case C1-C12-alkyl, preferably methyl, or halogen, preferably chlorine and/or bromine,
x in each case independently of one another, represents 0,1 or 2, p represents 1 or 0,
R1 and R2 can be chosen individually for each X1 and independently of one another represent hydrogen or C1-C6-alkyl, preferably hydrogen, methyl or ethyl,
X1 represents carbon and
m represents an integer from 4 to 7, preferably 4 or 5, with the proviso that on

at least one atom X1 R1 and R2 simultaneously represent alkyl are preferred.
Examples of bisphenols according to the general formula (I) are bisphenols which belong to the following groups: dihydroxydiphenyls, bis-(hydroxyphenyl)-alkanes, bis-(hydroxyphenyl)-cycloalkanes, indanebisphenols, bis-(hydroxyphenyl) sulfides,bis-(hydroxyphenyl) ethers, bis-(hydroxyphenyl) ketones, bis-(hydroxyphenyl) sulfones, bis-(hydroxyphenyl) sulfoxides and α,α1-bis-(hydroxyphenyl)-diisopropylbenzenes.
Derivatives of the bisphenols mentioned which are accessible, for example, by alkylation or halogenation on the aromatic rings of the bisphenols mentioned are also examples of bisphenols according to the general formula (I).
Examples of bisphenols according to the general formula (I) are, in particular, the
following compounds: hydroquinone, resorcinol, 4,4'-dihydroxydiphenyl, bis-(4-
hydroxyphenyl) sulfide, bis-(4-hydroxyphenyl) sulfone, bis-(3,5-dimethyl-4-
hydroxyphenyl)-methane, bis-(3,5-dimethyl-4-hydroxyphenyl) sulfone, l,l-bis-(3,5-
dimethyl-4-hydroxyphenyl)-p/rn-diisopropylbenzene, 1,1 -bis-(4-hydroxyphenyl)-1 -
phenyl-ethane, 1,1 -bis-(3,5-dimethyl-4-hydroxyphenyl)-cyclohexane, 1,1 -bis-(4-
hydroxyphenyl)-3-methylcyclohexane, 1,1 -bis-(4-hydroxyphenyl)-3,3-
dimethylcyclohexane, 1,1 -bis-(4-hydroxyphenyl)-4-methylcyclohexane, 1,1 -bis-(4-
hydroxyphenyl)-cyclohexane, 1,1 -bis-(4-hydroxyphenyl)-3,3,5-
trimethylcyclohexane, 2,2-bis-(3,5-dichloro-4-hydroxyphenyl)-propane, 2,2-bis-(3-
methyl-4-hydroxyphenyl)-propane, 2,2-bis-(3,5-dimethyl-4-hydroxyphenyl)-
propane, 2,2-bis-(4-hydroxyphenyl)-propane (i.e. bisphenol A), 2,2-bis-(3-chloro-4-hydroxyphenyl)-propane, 2,2-bis-(3,5-dibromo-4-hydroxyphenyl)-propane, 2,4-bis-(4-hydroxyphenyl)-2-methylbutane, 2,4-bis-(3,5-dimethyl-4-hydroxyphenyl)-2-methylbutane, α,α'-bis-(4-hydroxyphenyl)-o-diisopropylbenzene, α,α'-bis-(4-hydroxyphenyl)-m-diisopropylbenzene (i.e. bisphenol M), α,α'-bis-(4-hydroxyphenyl)-p-diisopropylbenzene and indanebisphenol.
Particularly preferred polycarbonates are the homopolycarbonate based on bisphenol A, the homopolycarbonate based on l,l-bis-(4-hydroxyphenyl)-3,3,5-trimethylcyclohexane and the copolycarbonates based on the two monomers bisphenol A and l,l-bis-(4-hydroxyphenyl)-3,3,5-trimethylcyclohexane.The bisphenols described, according to the general formula (I), can be prepared by known processes, e.g. from the corresponding phenols and ketones.
The bisphenols mentioned and processes for their preparation belong to the prior art., thus also l,l-bis-(4-hydroxyphenyl)-3,3,5-trimethylcyclohexane and the indanebisphenols. Indanebisphenols can be prepared, for example, from isopropenylphenol or derivatives thereof, or from dimers of isopropenylphenol or derivatives thereof in the presence of a Friedel-Crafts catalyst in organic solvents.
Polycarbonates can be prepared by known processes. Suitable processes for the preparation of polycarbonates are, for example, preparation from bisphenols with phosgene by the phase boundary process or from bisphenols with phosgene by the process in a homogeneous phase, the so-called pyridine process, or from bisphenols with carbonic acid esters by the melt transesterification process. These preparation processes are described e.g. in H. Schnell, "Chemistry and Physics of Polycarbonates", Polymer Reviews, volume 9, p. 31-76, Interscience Publishers, New York, London, Sydney, 1964.
The melt transesterification process is described, in particular, in H. Schnell, "Chemistry and Physics of Polycarbonates", Polymer Reviews, volume 9, p. 44 to 51, Interscience Publishers, New York, London, Sydney, 1964.
Raw materials and auxiliary substances with a low degree of impurities are preferably employed in the preparation of polycarbonate. In the preparation by the melt transesterification process in particular, the bisphenols employed and the carbonic acid derivatives employed should be as free as possible from alkali metal ions and alkaline earth metal ions. Raw materials of such purity are obtainable, for example, by recrystallizing, washing or distilling the carbonic acid derivatives, for example carbonic acid esters, and the bisphenols.The polycarbonates to be employed according to the invention preferably have a weight-average molecular weight (Mw), which can be determined e.g. by ultracentrifugation or scattered light measurement, of 10,000 to 200,000 g/mol. They particularly preferably have a weight-average molecular weight of 12,000 to 80,000 g/mol, especially preferably 20,000 to 35,000 g/mol.
The average molecular weight of the polycarbonates to be employed according to the invention can be established, for example, in a known manner by an appropriate amount of chain terminators. The chain terminators can be employed individually or as a mixture of various chain terminators.
Suitable chain terminators are both monophenols and monocarboxylic acids. Suitable monophenols are e.g. phenol, p-chlorophenol, p-tert-butylphenol, cumylphenol or 2,4,6-tribromophenol, and long-chain alkylphenols, such as e.g. 4-(l,l,3,3-tetramethylbutyl)-phenol, or monoalkylphenols or dialkylphenols having a total of 8 to 20 C atoms in the alkyl substituents, such as e.g. 3,5-di-tert-butylphenol, p-tert-octylphenol, p-dodecylphenol, 2-(3,5-dimethyl-heptyl)-phenol or 4-(3,5-dimethyl-heptyl)-phenol. Suitable monocarboxylic acids are benzoic acid, alkylbenzoic acids and halogenobenzoic acids.
Preferred chain terminators are phenol, p-tert-butylphenol, 4-(l,1,3,3-tetramethylbutyl)-phenol and cumylphenol.
The amount of chain terminators to be employed is preferably between 0.25 and 10 mol%, based on the total of the particular bisphenols employed.
The polycarbonates to be employed according to the invention can be branched in a known manner, and in particular preferably by incorporation of branching agents which are trifunctional or more than trifunctional. Suitable branching agents are e.g. those having three or more than three phenolic groups or those having three or more than three carboxylic acid groups.
Branching agents which are suitable according to the invention are, for example,
phloroglucinol, 4,6-dimethyl-2,4,6-tri-(4-hydroxyphenyl)-hept-2-ene, 4,6-dimethyl-
2,4,6-tri-(4-hydroxyphenyl)-heptane, 1,3,5-tri-(4-hydroxyphenyl)-benzene, 1,1,1-
tris-(4-hydroxyphenyl)-ethane, tri-(4-hydroxyphenyl)-phenyl-methane, 2,2-bis-[4,4-
bis-(4-hydroxyphenyl)-cyclohexyl]-propane, 2,4-bis-(4-hydroxyphenyl-isopropyl)-
phenol, 2,6-bis-(2-hydroxy-5'-methyl-benzyl)-4-methylphenol, 2-(4-
hydroxyphenyl)-2-(2,4-dihydroxyphenyl)-propane, hexa-(4-(4-hydroxyphenyl-
isopropyl)-phenyl) terephthalate, tetra-(4-hydroxyphenyl)-methane, tetra-(4-(4-
hydroxyphenyl-isopropyl)-phenoxy)-methane and l,4-bis-(4',4"-
dihydroxytriphenyl)-methylbenzene and 2,4-dihydroxybenzoic acid, trimesic acid, cyanuric chloride, 3,3-bis-(3-methyl-4-hydroxyphenyl)-2-oxo-2,3-dihydroindole, trimesic acid trichloride and o,a',Q!"-tris-(4-hydroxyphenyl)-l,3,5-triisopropylbenzene.Branching agents which are preferably to be employed are l,l,l-tris-(4-hydroxyphenyl)-ethane and 3,3-bis-(3-methyl-4-hydroxyphenyl)-2-oxo-2,3-dihydroindole.
The amount of the branching agents optionally to be employed is preferably 0.05 mol% to 2 mol%, based on the moles of bisphenols employed.
In the case of preparation of the polycarbonate by the phase boundary process, for example, the branching agents can be initially introduced into the aqueous alkaline phase with the bisphenols and the chain terminators, or they can be added as a solution in an organic solvent, together with the carbonic acid derivatives. In the case of the transesterification process, the branching agents are preferably metered in together with the dihydroxyaromatics or bisphenols.
Catalysts which are preferably to be employed in the preparation of polycarbonate by the melt transesterification process are the ammonium salts and phosphonium salts known from the literature.
Copolycarbonates can also be used according to the invention. Copolycarbonates in the context of the invention are, in particular, polydiorganosiloxane/polycarbonate block copolymers, the weight-average molecular weight (M w) of which is preferably 10,000 to 200,000 g/mol, particularly preferably 20,000 to 80,000 g/mol (determined by gel permeation chromatography after prior calibration by light scattering measurement or ultracentrifugation). The content of aromatic carbonate structural units in the polydiorganosiloxane/polycarbonate block copolymers is preferably 75 to 97.5 wt.%, particularly preferably 85 to 97 wt.%. The content of polydiorganosiloxane structural units in the polydiorganosiloxane/polycarbonate block copolymers is preferably 25 to 2.5 wt.%, particularly preferably 15 to 3 wt.%. The polydiorganosiloxane/polycarbonate block copolymers can be prepared, for example, starting from polydiorganosiloxanes containingα,ώ-bishydroxyaryloxy end groups and having an average degree of polymerization of preferably Pn = 5 to 100, particularly preferably Pn = 20 to 80.
The polydiorganosiloxane/polycarbonate block polymers can also be a mixture of polydiorganosiloxane/polycarbonate block copolymers -with conventional
polydiorganosiloxane structural units in this mixture preferably being 2.5 to 25 wt.%.
Such polydiorganosiloxane/polycarbonate block copolymers are characterized in that they contain in the polymer chain on the one hand aromatic carbonate structural units (I) and on the other hand polydiorganosiloxanes (2) containing aryloxy end groups
(Figure Removed)
are identical or different difunctional aromatic radicals and
R and R1 are identical or different and denote linear alkyl, branched alkyl, alkenyl, halogenated linear alkyl, halogenated branched alkyl, aryl or halogenated aryl, preferably methyl, and
denotes the average degree of polymerization of preferably 5 to 100,
particularly preferably 20 to 80.
Alkyl in the above formula (2) is preferably Ci-C2o-alkyl, alkenyl in the above formula (2) is preferably C2-C6-alkenyl; aryl in the above formulae (1) and (2) is preferably C6-C14-aryl. Halogenated in the above formula means partly or completely chlorinated, brominated or fluorinated.
Examples of alkyls, alkenyls, aryls, halogenated alkyls and halogenated aryls are methyl, ethyl, propyl, n-butyl, tert-butyl, vinyl, phenyl, naphthyl, chloromethyl, perfluorobutyl, perfluorooctyl and chlorophenyl.
Such polydiorganosiloxane/polycarbonate block copolymers and their preparation belong to the prior art.
Preferred polydiorganosiloxane/polycarbonate block copolymers can be prepared e.g. by reacting polydiorganosiloxanes containing α,ώ-bishydroxyaryloxy end

groups together with other bisphenols, optionally with the co-use of branching agents in the conventional amounts, e.g. by the two-phase boundary process (as described, for example, in H. Schnell, "Chemistry and Physics of Polycarbonates", Polymer Reviews, volume 9, p. 31-76, Interscience Publishers, New York, London, Sydney, 1964). The polydiorganosiloxanes containing o,oo-bishydroxyaryloxy end group used as educts for this synthesis and their preparation are described, for example, in US-A 3419 634.
Conventional additives, such as e.g. mould release agents, can be admixed to the polycarbonates in the melt or applied to the surface. The polycarbonates to be used preferably already comprise mould release agents before compounding with the other components of the moulding compositions according to the invention.
According to the invention, a graft polymer or a mixture of two or more graft copolymers which are obtained by grafting polymerization of at least one vinyl monomer on to a graft base based on olefinically unsaturated olefin polymers or olefinically unsaturated olefin copolymers are employed as component C).
According to the invention, graft polymers of
Cl) 5 to 95 wt.%, preferably 10 to 80 wt.%, in particular 20 to 50 wt.% of at least one vinyl monomer on
C2) 95 to 5 wt.%, preferably 90 to 20, in particular 80 to 20 wt.% of one or more graft bases having glass transitions temperatures of the rubber component of are employed as component C).

The graft base C2) in general has an average particle size (d50 value) of 0.05 to 5 μm, preferably 0.10 to 2 μm, particularly preferably 0.15 to 1 μm.
Monomers Cl) are preferably mixtures
Cl.l) of 50 to 99 parts by wt., preferably 60 to 80 parts by wt. of vinylaromatics and/or vinylaromatics substituted on the nucleus, such as styrene, a-methylstyrene, p-methylstyrene or p-chlorostyrene, and/or acrylic acid (C1-C8)-alkyl esters and/or methacrylic acid (Ci-Cg)-alkyl esters, such as methyl methacrylate and ethyl methacrylate, and
C1.2) 1 to 50 parts by wt., preferably 40 to 20 parts by wt. of vinyl cyanides (unsaturated nitriles, such as acrylonitrile and methacrylonitrile) and/or (meth)acrylic acid (C1-C8)-alkyl esters, such as methyl methacrylate, n-butyl acrylate and t-butyl acrylate, and/or derivatives, such as anhydrides and imides, of unsaturated carboxylic acids, for example maleic anhydride and N-phenylmaleimide.
Particularly preferred monomers Cl. 1) are chosen from at least one of the monomers styrene, a-methylstyrene and methyl methacrylate, and particularly preferred monomers C1.2) are chosen from at least one of the monomers acrylonitrile, maleic anhydride and methyl methacrylate.
Particularly preferred monomers are Cl.l styrene and C1.2 acrylonitrile and Cl.l styrene and C1.2 methyl methacrylate.
Preferred graft bases C2 are diene rubbers (e.g. based on butadiene, isoprene etc.) or mixtures of diene rubbers or copolymers of diene rubbers or mixtures thereof with further copolymerizable monomers (e.g. according to Cl.l and C1.2), with the proviso that the glass transition temperature of component C2 is below
preferably Pure polybutadiene rubber is particularly preferably employed.
Particularly preferred polymers C are e.g. ABS polymers (emulsion, bulk and suspension ABS) such as are known to the expert from the literature, for example from Ullmann, Enzyklopadie der Technischen Chemie, vol. 19 (1980), p. 280 et seq. The gel content of the graft base C2 is at least 30 wt.%, preferably at least 40 wt.% (measured in toluene).
The graft copolymers C) are prepared by free-radical polymerization, e.g. by emulsion, suspension, solution or bulk polymerization, preferably by emulsion or bulk polymerization.
ABS polymers which are prepared by redox initiation with an initiator system of organic hydroperoxide and ascorbic acid in accordance with US-A 4 937 285 are also particularly suitable graft rubbers.
Since as is known in the grafting reaction the grafting monomers are not necessarily completely grafted on to the graft base, according to the invention graft polymers C) are also understood as meaning those products which are obtained by (co)polymerization of the grafting monomers in the presence of the graft base and are co-obtained during the working up.
Products known to the expert as MBS rubbers, such as e.g. are marketed by Rohm und Haas under the name Paraloid® EXL 2600, Paraloid EXL 2650 or Paraloid® EXL 2691 and which are described e.g. in EP-A 0 985 682, are particularly preferred as polymers C).

According to the invention, one or a mixture of two or more graft copolymers which are obtained by grafting polymerization of at least one vinyl monomer on to a graft base based on rubber-elastic acrylate polymers or on rubber-elastic acrylate copolymers are employed as component D).
According to the invention, graft polymers of
Dl) 5 to 95 wt.%, preferably 10 to 80 wt.%, in particular 20 to 50 wt.% of at least one vinyl monomer on
D2) 95 to 5 wt.%, preferably 90 to 20, in particular 80 to 20 wt.% of one or more graft bases having glass transitions temperatures of the rubber component of are employed as component D).
The graft base D2) in general has an average particle size (djo value) of 0.05 to 5 fan, preferably 0.10 to 2 /mi, particularly preferably 0.15 to 1 μm.
Monomers Dl) are preferably mixtures
Dl.l) of 50 to 99, preferably 60 to 80 parts by wt. of vinylaromatics and/or vinylaromatics substituted on the nucleus, such as styrene, a-methylstyrene, p-methylstyrene or p-chlorostyrene, and/or acrylic acid (Ci-Cg)-alkyl esters and/or methacrylic acid (Ci-C8)-alkyl esters, such as methyl methacrylate and ethyl methacrylate, and
D1.2) 1 to 50, preferably 40 to 20 parts by wt. of vinyl cyanides (unsaturated nitriles, such as acrylonitrile and methacrylonitrile) and/or (meth)acrylic acid (C1-C8)-alkyl esters, such as methyl methacrylate, n-butyl acrylate and

t-butyl acrylate, and/or derivatives, such as anhydrides and imides, of unsaturated carboxylic acids, for example maleic anhydride and N-phenylmaleimide.
Particularly preferred monomers Dl.l) are chosen from at least one of the monomers styrene, a-methylstyrene and methyl methacrylate, and particularly preferred monomers D1.2) are chosen from at least one of the monomers acrylonitrile, maleic anhydride and methyl methacrylate.
Particularly preferred monomers are Dl.l styrene and D1.2 acrylonitrile.
Suitable acrylate rubbers according to D2 of the polymers D are, preferably, polymers of acrylic acid alkyl esters, optionally with up to 40 wt.%, based on D2, of other polymerizable, ethylenically unsaturated monomers. Preferred polymerizable acrylic acid esters include C1-C8-alkyl esters, for example the methyl, ethyl, butyl, n-octyl and 2-ethylhexyl ester, halogenoalkyl esters, preferably halogeno-C1-C8-alkyl esters, such as chloroethyl acrylate, and mixtures of these monomers.
For crosslinking, monomers having more than one polymerizable double bond can be copolymerized. Preferred examples of crosslinking monomers are esters of unsaturated monocarboxylic acids having 3 to 8 C atoms and unsaturated monohydric alcohols having 3 to 12 C atoms, or saturated polyols having 2 to 4 OH groups and 2 to 20 C atoms, such as e.g. ethylene glycol dimethacrylate and allyl methacrylate; polyunsaturated heterocyclic compounds, such as e.g. trivinyl and triallyl cyanurate; polyfunctional vinyl compounds, such as di- and trivinylbenzenes, dicyclopentadiene and 5-ethylidenenorbornene; and also triallyl phosphate and diallyl phthalate.
Preferred crosslinking monomers are allyl methacrylate, ethylene glycol dimethacrylate, diallyl phthalate and heterocyclic compounds which have at least 3 ethylenically unsaturated groups.

Particularly preferred crosslinking monomers are the cyclic monomers triallyl cyanurate, triallyl isocyanurate, triacryloylhexahydro-s-triazine and triallylbenzenes. The amount of the crosslinked monomers is preferably 0.02 to 5, in particular 0.05 to 2 wt.%, based on the graft base D2.
In the case of cyclic crosslinking monomers having at least 3 ethylenically unsaturated groups, it is advantageous to limit the amount to below 1 wt.% of the graft base D2.
Preferred "other" polymerizable, ethylenically unsaturated monomers which can optionally be used for the preparation of the graft base D2, in addition to the acrylic acid esters, are e.g. acrylonitrile, styrene, a-methylstyrene, acrylamides, vinyl C1-C6-alkyl ethers and methyl methacrylate. Preferred acrylate rubbers as the graft base D2 are emulsion polymers which have a gel content of at least 60 wt.%. The preparation of the graft base D2 can be carried out in one step or in several steps. A mixture of various graft bases according to the description can also be employed for the grafting reaction. In particular, various graft bases which differ in average particle size can also be employed.
ASA rubbers such as are described e.g. in WO 2000046296, in EP 0960145 or in DE 4229913 are particularly preferred as component D) according to the invention.
The compositions according to the invention comprise as component E) known UV stabilizers, such as are described, for example, in Gachter, Mtiller, Kunststoff-Additive, 3rd edition, Hanser-Verlag, Munich, Vienna, 1989 and in the Plastics Additives Handbook, 5th edition, Hanser-Verlag, Munich, 2001, p. 97-137, 141-154, 178-183, 188-192, 369-372 and 389-394. The UV stabilizers can be employed by themselves or in a mixture or in the form of masterbatches.

Preferred UV stabilizers which are to be employed according to the invention are sterically hindered phenols, sterically hindered amines (HALS = hindered amine light stabilizer), hydroquinones, aromatic secondary amines, such as diphenylamines, substituted resorcinols, salicylates, benzotriazoles and benzophenones, and variously substituted representatives of these groups and mixtures thereof.
Sterically hindered amines of the HALS type, benzotriazoles, benzotriazines and benzopyrimidines are particularly preferred.
The sterically hindered amines of the HALS type which are preferably to be employed can be derived from the general structure shown in (3)
(Figure Removed)
In this formula, the radicals can be, in each case independently of one another: Y: H, acyl, O radical, alkyl, alkenyl, alkoxyalkyl, arylalkyl,
X2: -OR, NR2, maleimide,
7 o
R and R independently of one another = H, alkyl, alkenyl, arylalkyl, preferably = H
R3, R4, R5, R6 independently of one another H, alkyl, phenyl, alkylaryl, aromatic heterocyclic radical containing oxygen, sulfur or nitrogen; preferably R3-R6 are methyl
The HALS stabilizers which are preferably to be employed are described, for example, in US 4895901, US 4210612 and US 5015682.
The benzotriazoles which are preferably to be employed can be derived generally from the structure shown in (4).

(Figure Removed)
In this formula, R9 and R10 can be chosen independently of one another from the group consisting of H, alkyl (in particular methyl, ethyl, propyl), cycloalkyl, halogen, haloalkyl, alkoxy, alkylene, aryl, alkyl-aryl or a combination of these.
Particularly preferably, R9 = R10 = (2-phenyl)-isopropyl, R9 = H and R10 = 2-(2,4,4-trimethyl)-pentyl, R9 = H and R10= methyl, R9 = R10 = t-butyl, R9 = t-butyl and R10 = methyl, R9 = R10 = 2-(2-methyl)-butyl, R9 = iso-butyl and R10 = 2-(2,4,4-trimethyl)-pentyl.
The benzotriazoles described which are preferably to be employed according to the invention are marketed, for example, by Ciba Spezialchemikalien, Basle, Switzerland under the commercial product name Tinuvin®.
The hydroxyphenyltriazine and -pyrimidine UV stabilizers which are preferably to be employed consist of two phenyl groups and one resorcinol group, which are bonded to a triazine or pyrimidine ring, as described in US 6 239 276 and US 5 597 854. The hydroxyphenyltriazines and -pyrimidines which are preferably to be employed can be derived generally from the general structure shown in (5).
In formula (5), A can be N or CH and R to R independently of one another can be chosen from the group consisting of H, alkyl (in particular methyl, ethyl, propyl), cycloalkyl, halogen, haloalkyl, alkoxy, alkylene, aryl, alkyl-aryl or combinations of these.
Examples of commercially available representatives of the hydroxyphenyltriazines which are preferably to be employed are Tinuvin® 1577 (CAS number 147315-50-2, Ciba Spezialchemikalien, Basle, Switzerland) or Cyasorb® UV 1164 (Cyctec Industries).
The compositions according to the invention comprise as component F) conventional colouring agents and/or pigments, such as e.g. titanium dioxide, ultramarine blue, iron oxide, carbon black, phthalocyanines, quinacridones, perylenes, nigrosin and anthraquinones and derivatives thereof. The colouring agents described in US-A 6 476 158 are also suitable, in particular, for improving the gloss after weathering. The colouring agents and/or pigments can be added as the substance or as a masterbatch, for example in component A), component B), component C), polyethylene, polypropylene, waxes or paraffin.
The colouring agents to be employed according to the invention are also described, for example, in Plastics Additives Handbook, 5th edition, Hanser-Verlag, Munich, 2001, p. 822-850.
According to the invention, the compositions can comprise as component G) at least difunctional, low molecular weight and oligomeric compounds which have at least one epoxide group.
Preferred epoxide-containing compounds as component G are, generally:
1. Polyglycidyl or poly-(jS-rnethylglycidyl) ethers obtainable by reaction of a compound having at least two free alcoholic or phenolic hydroxyl groups and/or phenolic hydroxyl groups and a suitably substituted epichlorohydrin under alkaline conditions, or in the presence of an acidic catalyst with subsequent treatment with alkali.
Ethers of this type are derived, for example, from acyclic alcohols, such as ethylene glycol, diethylene glycol and higher poly-(oxyethylene) glycols, propane-1,2-diol or poly-(oxypropylene) glycols, propane-1,3-diol, butane-1,4-diol, poly-(oxytetramethylene) glycols, pentane-1,5-diol, hexane-l,6-diol, hexane-2,4,6-triol, glycerol, 1,1,1-trimemylolpropane, bistrimethylolpropane, pentaerymritol and sorbitol, and from polyepichlorohydrins.
However, they are also derived, for example, from cycloaliphatic alcohols, such as 1,3- or 1,4-dihydroxycyclohexane, bis-(4-hydroxycyclohexyl)-methane, 2,2-bis-(4-hydroxycyclohexyl)-propane or l,l-bis-(hydroxymethyl)-cyclohex-3-ene, or they have aromatic nuclei, such as N,N-bis-(2-hydroxyethyl)-aniline or p,p'-bis-(2-hydroxyethyl-amino)-diphenylmethane.
The epoxide compounds can also be derived from mononuclear phenols, such as, for example, from resorcinol or hydroquinone; or they are based on polynuclear phenols, such as, for example, on bis-(4-hydroxyphenyl)-methane, 2,2-bis-(4-hydroxyphenyl)-propane, 2,2-bis-(3,5-dibromo-4-hydroxyphenyl)-propane or
4,4'-dihydroxydiphenyl sulfone, or on condensation products of phenols with formaldehyde which are obtained under acidic conditions, such as phenol-novolaks.
2. Difunctional, cycloaliphatic epoxide-containing compounds which contain the structural fragment shown in (6)

(Figure Removed)
In formula (6), R in each case independently of one another can be chosen from the group consisting of H, alkyl, aryl, halogen, halogenoalkyl, alkoxy, carboalkoxy and carbonyl, and n can be chosen from 0 to 8, preferably 0 to 2.
Preferred examples from the class of cycloaliphatic epoxide-containing compounds
which can optionally be employed according to the invention are 3,4-
epoxycyclohexyl 3,4-epoxycyclohexylcarboxylate (commercial product ERL 4221
from Union Carbide), bis-(3,4-epoxycyclohexylmethyl) adipate, vinylcyclohexene
diepoxide, 3,4-epoxy-6-methyl-cyclohexylmethyl 3',4'-epoxy-6'-
methylcyclohexanecarboxylate, 2,3-epoxycyclohexyl 3,4-
epoxycyclohexylcarboxylate, 4-(3,4-epoxy-5-methylcyclohexyl)-butyl 3',4'-epoxycyclohexylcarboxylate and 3,4-epoxy-cyclohexyl-ethylene oxide.
3. Poly-(N-glycidyl) compounds obtainable by dehydrochlorination of the reaction products of epichlorohydrin with amines. These amines are, for example, aniline, toluidine, n-butylamine, bis-(4-aminophenyl)-methane, m-xylylenediamine or bis-(4-methylaminophenyl)-methane, but also N,N,0-triglycidyl-m-aminophenol or N,N,O-triglycidyl-p-aminophenol.
The poly-(N-glycidyl) compounds also include, however, N,N'-diglycidyl derivatives of cycloalkylene-ureas, such as ethylene-urea or 1,3-propylene-urea, and N,N'-diglycidyl derivatives of hydantoins, such as of 5,5-dimethylhydantoin.
Nitrogen compounds which can preferably be employed are also nitrogen-containing heterocyclic compounds, such as triazines, barbituric acids, hydantoins, uracils, pyromellitic acid diimides, piperidines, piperazines, piperazinediones and isocyanurates.
The thermoplastic moulding compositions can comprise as component H) a filler or reinforcing substance or a mixture of two or more different fillers and/or reinforcing substances, for example based on talc, mica, silicate, quartz, titanium dioxide, wollastonite, kaolin, amorphous silicas, magnesium carbonate, chalk, feldspar, barium sulfate and glass beads, and/or fibrous fillers and/or reinforcing substances based on carbon fibres and/or glass fibres. Mineral particulate fillers based on talc, mica, silicate, quartz, titanium dioxide, wollastonite, kaolin, amorphous silicas, magnesium carbonate, chalk, feldspar, barium sulfate and/or glass fibres are preferably employed. According to the invention, mineral particulate fillers based on talc, wollastonite and/or glass fibres are particularly preferred. Fillers based on talc are most preferred.
For uses in particular in which isotropy in the dimensional stability and a high thermal dimensional stability is required, such as, for example, in motor vehicle uses for vehicle body exterior components, mineral fillers are preferably employed, particularly preferably talc, wollastonite or kaolin.
Needle-shaped mineral fillers are also particularly preferred. According to the invention, needle-shaped mineral fillers are understood as meaning a mineral filler with a highly pronounced needle-shaped character. Needle-shaped wollastonites may be mentioned as an example. The mineral preferably has a length : diameter ratio of 2:1 to 35:1, particularly preferably 3:1 to 19:1, most preferably 4:1 to 12:1.The average particle size of the needle-shaped minerals according to the invention is preferably less than 20 μm, particularly preferably less than 15 μm, especially preferably less than 10 μm, most preferably less than 5 μm, determined with a CILAS GRANULOMETER.
Mineral fillers based on talc are most preferred as component H). In the context of the invention, possible mineral fillers based on talc are all the particulate fillers which the expert associates with talc or talcum. All the particulate fillers which are commercially available and have product descriptions which contain the terms talc or talcum as characterizing features are also possible.
Mineral fillers which have a content of talc according to DIN 55920 of greater than 50 wt.%, preferably greater than 80 wt.%, particularly preferably greater than 95 wt.% and especially preferably greater than 98 wt.%, based on the total weight of filler, are preferred.
The mineral fillers based on talc can also be treated on the surface. For example, they can be finished with an adhesion promoter system e.g. based on silane.
The mineral fillers to be employed according to the invention which are based on talk preferably have an upper particle or grain size d97 of less than 50 μm, preferably less than 10 μm, particularly preferably less than 6μm and especially preferably less than 2.5 μm. The average particle size d50 chosen is preferably a value of less than 10 μrn, preferably less than 6 μm, particularly preferably less than 2 /an and especially preferably less than 1 μm. The d97 and d50 values of the fillers are determined by SEDIGRAPH D 5 000 sedimentation analysis or by DIN 66 165 sieve analysis.
The average aspect ratio (diameter to thickness) of the particulate fillers based on talc is preferably in the range from 1 to 100, particularly preferably 2 to 25 and especially preferably 5 to 25, determined on electron microscopy photographs ofultra-thin sections of the finished products and by measurement of a representative amount (approx. 50) of filler particles.
The filler and/or reinforcing substance can optionally be modified on the surface, for example with an adhesion promoter or adhesion promoter system, e.g. based on silane. However, the pretreatment is not absolutely necessary. In particular, if glass fibres are used polymer dispersions, film-forming agents, branching agents and/or glass fibre processing auxiliaries can also be used in addition to silanes.
According to the invention, glass fibres which in general have a fibre diameter of between 7 and 18 μm, preferably between 9 and 15 μm, can also be particularly preferably employed. These can be added as continuous fibres or as cut or ground glass fibres, it being possible for the fibres to be finished with a suitable size system and an adhesion promoter or adhesion promoter system, e.g. based on silane.
Customary silane compounds for pretreatment with a size system have, for example, the general formula
in which the substituents have the following meaning:
(Figure Removed)
q an integer from 2 to 10, preferably 3 to 4
r an integer from 1 to 5, preferably 1 to 2
k an integer from 1 to 3, preferably 1.
Preferred silane compounds are aminopropyltrimethoxysilane, aminobutyltrimethoxysilane, aminopropyltriethoxysilane, aminobutyltriethoxysilane and the corresponding silanes which contain a glycidyl group as the substituent X.
The silane compounds can in general be employed for the surface coating in amounts of 0.05 to 2 wt.%, preferably 0.5 to 1.5 wt.% and in particular 0.8 to 1 wt.%, based on the mineral filler.
Due to the processing to give the moulding composition or shaped article, the particulate fillers can have a lower d97 or d50 value in the moulding composition or in the shaped article than the fillers originally employed. Due to the processing to give the moulding composition or shaped article, the glass fibres can have shorter length distributions in the moulding composition or in the shaped article than originally employed.
The particle diameter in the finished product can be determined here, for example, by recording electron microscopy photographs of thin sections of the polymer mixture and using at least 25, preferably at least 50 filler particles for the evaluation.
The compositions according to the invention can furthermore comprise as component I) conventional additives, which in general can be added in amount of up to 15 wt.%, preferably in an amount of 0.01 to 10 wt.%, particularly preferably 0.05 to 5 wt.%, especially preferably 0.1 to 3 wt.%, based on the total weight of the moulding compositions.
All the conventional additives, such as e.g. stabilizers (for example heat stabilizers), antistatics, flow agents, mould release agents, fireproofing additives, emulsifiers, nucleating agents, plasticizers, lubricants, additives which lower the pH (e.g. compounds containing carboxyl groups) and additives for increasing the conductivity can be possible here. The additives mentioned and further suitable additives are described, for example, in Gachter, Miiller, Kunststoff-Additive, 3rdedition, Hanser-Verlag, Munich, Vienna, 1989. The additives can be employed by themselves or as a mixture or in the form of masterbatches. The additives can be admixed and/or applied to the surface.
Stabilizers which can be employed are, for example, sterically hindered phenols and/or phosphites, hydroquinones, aromatic secondary amines, such as diphenylamines, substituted resorcinols, salicylates, benzotriazoles and benzophenones, and variously substituted representatives of these groups and mixtures thereof.
Nucleating agents which can be employed are e.g. sodium phenyl phosphinate, aluminium oxide, silicon dioxide and, preferably talc and the nucleating agents described above.
Lubricants and mould release agents which can be employed are ester waxes, pentaerithrityl stearate (PETS), long-chain fatty acids (e.g. stearic acid or behenic acid), their salts (e.g. Ca or Zn stearate) and amide derivatives (e.g. ethylene-bis-stearylamide) or montan waxes (mixtures of straight-chain, saturated carboxylic acids having chain lengths of 28 to 32 C atoms) and low molecular weight polyethylene or polypropylene waxes.
Plasticizers which can be employed are, for example, phthalic acid dioctyl ester, phthalic acid dibenzyl ester, phthalic acid butyl benzyl ester, hydrocarbon oils and N-(n-butyl)benzenesulfonamide.
In order to obtain conductive moulding compositions, carbon blacks, conductivity blacks, carbon fibrils, nanoscale graphite fibres (nanotubes), graphite, conductive polymers, metal fibres and other conventional additives for increasing the conductivity can be added.
Flameproofing agents which can be employed are commercially available organic halogen compounds with synergists or commercially available organic nitrogen compounds or organic/inorganic phosphorus compounds, individually or in a mixture. Mineral flameproofing additives, such as magnesium hydroxide or Ca/Mg carbonate hydrates (e.g. DE-A 4 236 122) can also be employed. Examples of halogen-containing, in particular brominated and chlorinated compounds which may be mentioned are: ethylene-l,2-bistetrabromophthalimide, epoxidized tetrabromobisphenol A resin, tetrabromobisphenol A oligocarbonate, tetrachlorobisphenol A oligocarbonate, pentabromopolyacrylate and brominated polystyrene. Suitable organic phosphorus compounds are the phosphorus compounds according to WO-A 98/17720, e.g. triphenyl phosphate (TPP), resorcinol bis-(diphenyl phosphate), including oligomers, and bisphenol A bis-diphenyl phosphate, including oligomers (cf. e.g. EP-A 0 363 608 and EP-A 0 640 655), melamine phosphate, melamine pyrophosphate, melamine polyphosphate and mixtures thereof. Possible nitrogen compounds are, in particular, melamine and melamine cyanurate. Suitable synergists are e.g. antimony compounds, in particular antimony trioxide and antimony pentoxide, zinc compounds, tin compounds, such as e.g. tin stannate, and borates. Carbon-forming agents and tetrafluoroethylene polymers can be added. The flameproofing agents, optionally with a synergist, such as antimony compounds, and antidripping agents, are in general employed in an amount of up to 30 wt.%, preferably 20 wt.% (based on the total composition).
Reinforcing substances, e.g. in the form of glass fibres, can also be added as additives.
The invention furthermore provides a process for the preparation of the compositions, the use of the composition according to the invention for the production of semi-finished products and mouldings and semi-finished products and mouldings produced therefrom.
The compositions according to the invention are prepared by known processes by mixing the components. It may be advantageous to premix individual components. The premixing can take place here both as a dry blend and by joint kneading, extrusion or milling of the components. Mixing in of individual components, in particular stabilizers, additives and colouring agents, can furthermore already be carried out during synthesis of the polymers employed according to the invention. Mixing of components A to D and further constituents is preferably effected at temperatures of 220 to 330 °C by joint kneading, extrusion or milling of the components.
The compositions according to the invention can be processed to all types of semifinished products or moulding by conventional processes. Examples of processing processes which may be mentioned are extrusion processes and injection moulding processes. Examples of semi-finished products which may be mentioned are films and sheets.
Because of the high colour homogeneity, the mouldings are particularly suitable for uses which are visually and optically important. According to the invention, the mouldings can be employed in a non-lacquered form or in a form coated with a transparent clear lacquer system. However, the mouldings can of course also be lacquered with a colouring base lacquer. The mouldings can be small or large components and can be employed for exterior or interior uses. Preferably, large-component mouldings are produced for vehicle construction, in particular the automobile sector. In particular, vehicle body exterior components, such as e.g. mud guards, tail gates, engine bonnets, bumpers, loading areas, covers for loading areas, car roofs, air intake grills, spoilers or other vehicle body components, can be produced from the moulding compositions according to the invention.
Mouldings or semi-finished products from the moulding compositions/compositions according to the invention can also be in a composite with further materials, such as e.g. metal or plastic. The moulding compositions according to the invention or themouldings/semi-finished products from the moulding compositions according to the invention can be employed in a composite with other materials or with themselves for the production of finished components, such as e.g. vehicle body exterior components, by conventional techniques of bonding and joining of several components or parts, such as e.g. coextrusion, injection moulding under films, injection moulding around embedded components, gluing, welding, screwing or clamping.
The moulding compositions according to the invention can also be used for numerous further uses. Examples which may be mentioned are the use in electrical and electronics engineering and in the construction sector. Mouldings from the moulding compositions according to the invention can be used in the fields of use mentioned, for example, as lamp covers, as safety panes, as housing material for electronic apparatuses, as housing material for domestic appliances and as sheets for the production of covers.
The compositions according to the invention are distinguished by a very good colour homogeneity and by a very good stability to weathering. They moreover fulfil high requirements with regard to processing stability, flowability of the melt, toughness, toughness at low temperatures, rigidity, heat distortion point, thermal expansion, surface quality, lacquerability, resistance to chemicals and resistance to fuels.
Examples Component A
Polybutylene terephthalate type Al: Component A is polybutylene terephthalate having an intrinsic viscosity IV of 0.93 cm3/g, commercial product Pocan® B1300 from Bayer AG, Leverkusen.
The intrinsic viscosity is measured in phenol/o-dichlorobenzene (1:1 parts by wt.) at
25 °C.
Component B
Polycarbonate type Bl:
Linear polycarbonate (Makrolon® 2405 from Bayer AG, Leverkusen, Germany) based on bisphenol A having a viscosity )?rel. of approx. 1.29 (measurement conditions: 5 g polycarbonate per litre of methylene chloride, 25 °C) and a molecular weight Mw of approx. 29,000 g/mol (determined with GPC methods against a polycarbonate standard).
Component Cl
Component Cl is Paraloid® EXL 2650 from Rohm und Haas Deutschland GmbH, Frankfurt.
Component C2
Component C2 is a graft copolymer of acrylonitrile and styrene on a graft base of polybutadiene, intermediate product of Bayer AG, Leverkusen having a polybutadiene content of 75 wt.% and a styrene content in the shell of 28 wt.%.
Comparison component VI
Comparison component VI is the AES rubber Royaltuf® 970 E (former name Blendex® WX 270) from Crompton Corporation, Crompton GmbH Deutschland, Bergkamen.
Component Dl
Component Dl is a graft copolymer of acrylonitrile and styrene on a graft base of partly crosslinked polybutyl acrylate, Centrex® 57 WBA, intermediate product of Bayer Corp., Pittsburgh.
Component D2
Component D2 is Paraloid® EXL 3361 (a core/shell impact modifier based on a partly crosslinked acrylate core) from Rohm & Haas Deutschland, Frankfurt.
Component E
Component E is Tinuvin® 350 from Ciba Geigy, Basle.
Component F
Component F is carbon black, type Black Pearls® 800 from Cabot GmbH, Hanau.
Component G
Component G is Araldit® GT 7071 (hydrolysis stabilizer based on a phenol/epichlorohydrin reaction product) from Huntsman Advanced Materials Deutschland GmbH, Bergkamen.
In addition, commercially available processing auxiliaries are employed as additives.
Compounding operations were carried out on a twin-screw extruder of the type ZSK32 (Werner und Pfleiderer) at melt temperatures of 250 to 290 °C.
The test specimens were injection moulded on an injection moulding machine of the type Arburg 320-210-500 at melt temperatures of 260 to 280 °C and mould temperatures of 70 to 90 °C.
The moulding compositions according to the invention were tested by the following methods:
Vicat B: Heat distortion stability or heat distortion point in accordance with DIN ISO 306/B 120 in silicone oil.
Izod impact strength: Toughness in accordance with ISO 180 method 1 U at -30 °C.
Izod notched impact strength: Toughness in accordance with ISO 180 method 1 A at 23 °C.
Tensile E modulus and tensile strength in accordance with DIN / EN / ISO 527-2/1 A.
MVR: Flowability in accordance with DIN/ISO 1133 at 260 °C and 5 kg.
Colour homogeneity: Determination of the colour homogeneity of the surface by visual assessment.
"+" means a homogeneous coloration without the formation of stripes of lower colour intensity perpendicular to the direction of flow (tiger stripes)"0" means a largely homogenous coloration with slight formation of stripes of lower colour intensity perpendicular to the direction of flow
"-" means an inhomogeneous coloration with severe formation of stripes perpendicular to the direction of flow.
The evaluation of the colour homogeneity was carried out on sheets of 150 x 105 x 1.6 mm, which were produced with a melt temperature of 270 °C, a mould temperature of 80 °C and a filling rate of 50 mm/s via a film gate on a 105 mm side.
As can be seen from table 1, the moulding compositions according to the invention have the required combination of very good colour homogeneity and good stability to hydrolysis (>60% of the initial tensile strength after hydrolysis) with simultaneously good mechanical properties. Compared with comparison examples 2 and 3, the moulding compositions according to the invention moreover are significantly more stable to UV, because the content of UV-sensitive components C is significantly lower.
The composition and properties of the thermoplastic moulding compositions according to the invention can be seen from table 1.
(Table Removed)

We Claim:
1. Composition consisting of
(A) 4 to 80 parts by wt. of a polyalkylene terephthalate,
(B) 10 to 90 parts by wt. of a aromatic polycarbonate,
(C) 1.5 to 30 parts by wt. of a graft polymer based on polybutadiene as the rubber component,
(D) 1.5 to 30 parts by wt. of a graft polymer based on acrylates as the rubber component,
(E) 0.01 to 5 parts by wt. of UV stabilizers of the kind such as herein described,
(F) 0.01 to 10 parts by wt. of colouring agent of the kind such as herein described,
(G) 0 to 5 parts by wt. of hydrolysis stabilizers of the kind such as herein described,
(H) 0 to 54 parts by wt. of a particulate mineral filler of the kind such as herein
described, (I) 0 to 10 parts by wt. of further additives of the kind such as herein described.
2. Composition as claimed in claim 1, wherein C) is composed of graft polymers of
C1) 5 to 95 wt.% of at least one vinyl monomer on
C2) 95 to 5 wt.% of one or more graft bases having glass transition temperatures of the rubber component of 3. Composition as claimed in claim 1 or 2, wherein C1) is a mixture of
C1.1) 50 to 99 parts by wt. of styrene, α-methylstyrene, ß-methylstyrene, p-chlorostyrene and /or acrylic acid (C1-C8)-alkyl esters and/or methacrylic acid (C1-C8)-alkyl esters and
C1.2) 1 to 50 parts by wt. of vinyl cyanides and/or (meth)acrylic acid (C1-C8)-alkyl esters and/or anhydrides and imides of unsaturated carboxylic acids.
4. Composition as claimed in claim 1 or 2, wherein D) is composed of graft polymer of
D1) 5 to 95 wt.% of at least one vinyl monomer on
D2) 95 to 5 wt.% of one or more graft bases having glass transition temperatures of the rubber component of
5. Compositions as claimed in one or more of the preceding claims, wherein polyethylene
terephthalate is employed as component A.
6. The composition as claimed in claim 1 as and when used to prepare mouldings and semifinished products.

Documents:

2114-DELNP-2006-Abstract-(30-11-2011).pdf

2114-delnp-2006-abstract.pdf

2114-DELNP-2006-Claims-(30-11-2011).pdf

2114-delnp-2006-claims.pdf

2114-DELNP-2006-Correspondence Others-(14-07-2011).pdf

2114-DELNP-2006-Correspondence Others-(30-11-2011).pdf

2114-delnp-2006-correspondence-others-1.pdf

2114-delnp-2006-correspondence-others.pdf

2114-DELNP-2006-Description (Complete)-(30-11-2011).pdf

2114-delnp-2006-description(complete).pdf

2114-DELNP-2006-Form-1-(30-11-2011).pdf

2114-delnp-2006-form-1.pdf

2114-delnp-2006-form-18.pdf

2114-DELNP-2006-Form-2-(30-11-2011).pdf

2114-delnp-2006-form-2.pdf

2114-DELNP-2006-Form-3-(14-07-2011).pdf

2114-delnp-2006-form-3.pdf

2114-delnp-2006-form-5.pdf

2114-DELNP-2006-GPA-(30-11-2011).pdf

2114-delnp-2006-gpa.pdf

2114-delnp-2006-pct-210.pdf

2114-delnp-2006-pct-304.pdf

2114-delnp-2006-pct-306.pdf

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Patent Number

250504

Indian Patent Application Number

2114/DELNP/2006

PG Journal Number

02/2012

Publication Date

13-Jan-2012

Grant Date

06-Jan-2012

Date of Filing

19-Apr-2006

Name of Patentee

BAYER MATERIALSCIENCE AG

Applicant Address

51368 LEVERKUSEN, GERMANY.

Inventors:

#	Inventor's Name	Inventor's Address
1	PETER PERSIGEHL	VENICE 42 WUXI TAIHU VENICE GARDEN, WUXI,JIANGSU 214121, CHINA.
2	PAULFRIEDMANN,	PETER-WALTERSCHEIDT-STR. 65,51469 BERGISCH GLADBACH, GERMANY;
3	URS-PETER DORSCH	PFAUENSTR.38,41540 DORMAGEN, GERMANY;
4	HANS-JURGEN THIEM	KONIGSBERGER STR. 11,41539 DORMAGEN, GERMANY

PCT International Classification Number

C08L 67/02

PCT International Application Number

PCT/EP2004/012901

PCT International Filing date

2004-11-13

PCT Conventions:

#	PCT Application Number	Date of Convention	Priority Country
1	103 53 830.5	2003-11-18	Germany