Thermoplastic polycarbonate compositions, method of manufacture, and method of use thereof

Abstract

A thermoplastic composition comprising in combination an aliphatic/aromatic co-polycarbonate component; an impact modifier; and a rigid copolymer, and optionally a polycarbonate component and/or a polycarbonate-polysiloxane copolymer is disclosed. The co-polycarbonate comprises repeating carbonate units and repeating aliphatic units. The compositions have a significantly improved balance of properties, including melt flow and impact.

Description

BACKGROUND

This invention is directed to thermoplastic compositions comprising aromatic polycarbonate, their method of manufacture, and method of use thereof, and in particular impact-modified thermoplastic polycarbonate compositions having improved stability.

Aromatic polycarbonates are useful in the manufacture of articles and components for a wide range of applications, from automotive parts to electronic appliances. Impact modifiers are commonly added to aromatic polycarbonates to improve the toughness of the compositions. The impact modifiers often have a relatively rigid thermoplastic phase and an elastomeric (rubbery) phase, and may be formed by bulk or emulsion polymerization. Polycarbonate compositions comprising acrylonitrile-butadiene-styrene (ABS) impact modifiers are described generally, for example, in U.S. Pat. No. 3,130,177 and U.S. Pat. No. 3,130,177. Polycarbonate compositions comprising emulsion polymerized ABS impact modifiers are described in particular in U.S. Publication No. 2003/0119986. U.S. Publication No. 2003/0092837 discloses use of a combination of a bulk polymerized ABS and an emulsion polymerized ABS.

Of course, a wide variety of other types of impact modifiers for use in polycarbonate compositions have also been described. While suitable for their intended purpose of improving toughness, many impact modifiers may also adversely affect other properties, such as processability, hydrolytic stability, and/or low temperature impact strength, particularly upon prolonged exposure to high humidity and/or high temperature such as may be found in Southeast Asia. Thermal aging stability of polycarbonate compositions, in particular, is often degraded with the addition of rubbery impact modifiers. There remains a continuing need in the art, therefore, for impact-modified thermoplastic polycarbonate compositions having a combination of good properties, including melt flow, toughness and hydrolytic stability. It would further be advantageous if melt flow could be improved without significantly adversely affecting other desirable properties of polycarbonates, such as impact.

SUMMARY OF THE INVENTION

In one embodiment, a thermoplastic composition comprises in combination in combination an aliphatic/aromatic co-polycarbonate component; an impact modifier; and a rigid copolymer, such as an aromatic vinyl copolymer, and optionally a polycarbonate and/or a polycarbonate-polysiloxane copolymer. In an embodiment, wherein the thermoplastic composition has a melt volume rate (MVR) of at least 13 cm³/10 minutes, specifically at least 20 cm³/10 minutes, when measured at 260° C. using a 5-kilogram weight, with a six minute preheat, according to ASTM D1238.

In another embodiment, an article comprises the above thermoplastic composition. In an embodiment, the article has a surface gloss level measured on a textured surface of less than 15, specifically less than 10, when measured on a textured surface according to ASTM D2457 at 60° using a Gardner Gloss Meter and 3 millimeter color chips. In an embodiment, the surface gloss level is measured on a textured surface selected from commercially available surfaces, including, for example, MT11030 (a fine texture); Montana Texture (a coarse texture); Rochester Texture; 1055-2 Texture; N122 Texture; and N111 Texture.

In still another embodiment, a method of manufacture of an article comprises molding, extruding, or shaping the above thermoplastic composition.

In still another embodiment, a method for the manufacture of a thermoplastic composition having improved hydrolytic and/or thermal stability, the method comprising admixture of an aliphatic/aromatic co-polycarbonate component; an impact modifier; and a rigid copolymer, such as an aromatic vinyl copolymer, and optionally a polycarbonate and/or a polycarbonate-polysiloxane copolymer.

BRIEF DESCRIPTION OF THE FIGURE

FIG. 1 is a plot of the response surface showing the relationship between composition and melt flow, using the data from the Examples in Table 2, as input into a statistical modeling package.

DETAILED DESCRIPTION OF THE INVENTION

It has been discovered by the inventors hereof that use of a particular type of aliphatic/aromatic co-polycarbonate in impact modified blends of polycarbonate provides a greatly improved balance of properties to thermoplastic compositions, while at the same time maintaining their thermal stability and/or impact resistance. The improvement in melt flow without significantly adversely affecting impact or other properties, such as gloss, is particularly unexpected. It has further been discovered that an advantageous combination of other physical properties can be obtained.

The particular aliphatic/aromatic co-polycarbonate comprises blocks of repeating carbonate units and blocks of repeating aliphatic units, as further described below.

In one embodiment, the particular aliphatic/aromatic co-polycarbonate is prepared by reacting a dihydroxy aromatic compound under interfacial conditions with phosgene and an aliphatic chloroformate, wherein the aliphatic chloroformate is prepared by a method comprising introducing a mixture of at least one functional aliphatic compound, phosgene, a solvent, and optionally at least one organic base into a flow reactor to obtain a unidirectional flowing reaction mixture. The co-polycarbonate will be described in further detail below.

In another embodiment, the particular aliphatic/aromatic co-polycarbonate is derived from a dihydric phenol, a carbonate precursor and an aliphatic alpha, omega-dicarboxylic acid or ester precursor, wherein the aliphatic alpha, omega-dicarboxylic acid or ester precursor has from 6 to about 20 carbon atoms and is present in the co-polycarbonate in an amount of from about 2 to about 30 mole percent of the dihydric phenol. The co-polycarbonate will be described in further detail below.

As used herein, the terms “polycarbonate” and “polycarbonate resin” means compositions having repeating structural carbonate units of formula (1): in which at least about 60 percent of the total number of R¹ groups are aromatic organic radicals and the balance thereof are aliphatic, alicyclic, or aromatic radicals. In one embodiment each R¹ is an aromatic organic radical and, more specifically, a radical of formula (2): A¹-Y¹-A²-   (2) wherein each of A¹ and A² is a monocyclic divalent aryl radical and Y¹ is a bridging radical having one or two atoms that separate A¹ from A². In an exemplary embodiment, one atom separates A¹ from A². Illustrative non-limiting examples of radicals of this type are —O—, —S—, —S(O)—, —S(O₂)—, —C(O)—, methylene, cyclohexylmethylene, 2-[2.2.1]-bicycloheptylidene, ethylidene, isopropylidene, neopentylidene, cyclohexylidene, cyclopentadecylidene, cyclododecylidene, and adamantylidene. The bridging radical Y¹ may be a hydrocarbon group or a saturated hydrocarbon group such as methylene, cyclohexylidene, or isopropylidene.

Polycarbonates may be produced by the interfacial reaction of dihydroxy compounds having the formula HO—R¹—OH, which includes dihydroxy compounds of formula (3) HO-A¹-Y¹-A²-OH   (3) wherein Y¹, A¹ and A² are as described above. Also included are bisphenol compounds of general formula (4): wherein R^a and R^b each represent a halogen atom or a monovalent hydrocarbon group and may be the same or different; p and q are each independently integers of 0 to 4; and X^a represents one of the groups of formula (5): wherein R^c and R^d each independently represent a hydrogen atom or a monovalent linear or cyclic hydrocarbon group and R^e is a divalent hydrocarbon group.

Some illustrative, non-limiting examples of suitable dihydroxy compounds include the following: resorcinol, 4-bromoresorcinol, hydroquinone, alkyl-substituted hydroquinone such as methylhydroquinone, 4,4′-dihydroxybiphenyl, 1,6-dihydroxynaphthalene, 2,6-dihydroxynaphthalene, bis(4-hydroxyphenyl)methane, bis(4-hydroxyphenyl)diphenylmethane, bis(4-hydroxyphenyl)-1-naphthylmethane, 1,2-bis(4-hydroxyphenyl)ethane, 1,1-bis(4-hydroxyphenyl)-1-phenylethane, 2-(4-hydroxyphenyl)-2-(3-hydroxyphenyl)propane, bis(4-hydroxyphenyl)phenylmethane, 2,2-bis(4-hydroxy-3-bromophenyl)propane, 1,1-bis(hydroxyphenyl)cyclopentane, 1,1-bis(4-hydroxyphenyl)cyclohexane, 1,1-bis(4-hydroxyphenyl)isobutene, 1,1-bis(4-hydroxyphenyl)cyclododecane, trans-2,3-bis(4-hydroxyphenyl)-2-butene, 2,2-bis(4-hydroxyphenyl)adamantine, (alpha, alpha′-bis(4-hydroxyphenyl)toluene, bis(4-hydroxyphenyl)acetonitrile, 2,2-bis(3-methyl-4-hydroxyphenyl)propane, 2,2-bis(3-ethyl-4-hydroxyphenyl)propane, 2,2-bis(3-n-propyl-4-hydroxyphenyl)propane, 2,2-bis(3-isopropyl-4-hydroxyphenyl)propane, 2,2-bis(3-sec-butyl-4-hydroxyphenyl)propane, 2,2-bis(3-t-butyl-4-hydroxyphenyl)propane, 2,2-bis(3-cyclohexyl-4-hydroxyphenyl)propane, 2,2-bis(3-allyl-4-hydroxyphenyl)propane, 2,2-bis(3-methoxy-4-hydroxyphenyl)propane, 2,2-bis(4-hydroxyphenyl)hexafluoropropane, 1,1-dichloro-2,2-bis(4-hydroxyphenyl)ethylene, 1,1-dibromo-2,2-bis(4-hydroxyphenyl)ethylene, 1,1-dichloro-2,2-bis(5-phenoxy-4-hydroxyphenyl)ethylene, 4,4′-dihydroxybenzophenone, 3,3-bis(4-hydroxyphenyl)-2-butanone, 1,6-bis(4-hydroxyphenyl)-1,6-hexanedione, ethylene glycol bis(4-hydroxyphenyl)ether, bis(4-hydroxyphenyl)ether, bis(4-hydroxyphenyl)sulfide, bis(4-hydroxyphenyl)sulfoxide, bis(4-hydroxyphenyl)sulfone, 9,9-bis(4-hydroxyphenyl)fluorine, 2,7-dihydroxypyrene, 6,6′-dihydroxy-3,3,3′,3′-tetramethylspiro(bis)indane (“spirobiindane bisphenol”), 3,3-bis(4-hydroxyphenyl)phthalide, 2,6-dihydroxydibenzo-p-dioxin, 2,6-dihydroxythianthrene, 2,7-dihydroxyphenoxathin, 2,7-dihydroxy-9,10-dimethylphenazine, 3,6-dihydroxydibenzofuran, 3,6-dihydroxydibenzothiophene, and 2,7-dihydroxycarbazole, and the like. Combinations comprising at least one of the foregoing dihydroxy compounds may also be used.

A nonexclusive list of specific examples of the types of bisphenol compounds that may be represented by formula (3) includes 1,1-bis(4-hydroxyphenyl) methane, 1,1-bis(4-hydroxyphenyl) ethane, 2,2-bis(4-hydroxyphenyl) propane (hereinafter “bisphenol A” or “BPA”), 2,2-bis(4-hydroxyphenyl) butane, 2,2-bis(4-hydroxyphenyl) octane, 1,1-bis(4-hydroxyphenyl) propane, 1,1-bis(4-hydroxyphenyl) n-butane, 2,2-bis(4-hydroxy-1-methylphenyl) propane, and 1,1-bis(4-hydroxy-t-butylphenyl) propane. Combinations comprising at least one of the foregoing bisphenol compounds may also be used.

Branched polycarbonates are also useful, as well as blends comprising a linear polycarbonate and a branched polycarbonate. The branched polycarbonates may be prepared by adding a branching agent during polymerization, for example a polyfunctional organic compound containing at least three functional groups selected from hydroxyl, carboxyl, carboxylic anhydride, haloformyl, and mixtures of the foregoing functional groups. Specific examples include trimellitic acid, trimellitic anhydride, trimellitic trichloride, tris-p-hydroxyphenylethane, isatin-bis-phenol, tris-phenol TC (1,3,5-tris((p-hydroxyphenyl)isopropyl)benzene), tris-phenol PA (4(4(1,1-bis(p-hydroxyphenyl)-ethyl) alpha, alpha-dimethyl benzyl)phenol), 4-chloroformyl phthalic anhydride, trimesic acid, and benzophenone tetracarboxylic acid. The branching agents may be added at a level of about 0.05-2.0 wt. %. All types of polycarbonate end groups are contemplated as being useful in the polycarbonate composition, provided that such end groups do not significantly affect desired properties of the thermoplastic compositions.

Suitable polycarbonates can be manufactured by processes such as interfacial polymerization and melt polymerization. Although the reaction conditions for interfacial polymerization may vary, an exemplary process generally involves dissolving or dispersing a dihydric phenol reactant in aqueous caustic soda or potash, adding the resulting mixture to a suitable water-immiscible solvent medium, and contacting the reactants with a carbonate precursor in the presence of a suitable catalyst such as triethylamine or a phase transfer catalyst, under controlled pH conditions, e.g., about 8 to about 10. The most commonly used water immiscible solvents include methylene chloride, 1,2-dichloroethane, chlorobenzene, toluene, and the like. Suitable carbonate precursors include, for example, a carbonyl halide such as carbonyl bromide or carbonyl chloride, or a haloformate such as a bishaloformates of a dihydric phenol (e.g., the bischloroformates of bisphenol A, hydroquinone, and the like) or a glycol (e.g., the bishaloformate of ethylene glycol, neopentyl glycol, polyethylene glycol, and the like). Combinations comprising at least one of the foregoing types of carbonate precursors may also be used.

Among the exemplary phase transfer catalysts that may be used are catalysts of the formula (R³)₄Q⁺X, wherein each R³ is the same or different, and is a C_1-10 alkyl group; Q is a nitrogen or phosphorus atom; and X is a halogen atom or a C_1-8 alkoxy group or C_6-18 aryloxy group. Suitable phase transfer catalysts include, for example, [CH₃(CH₂)₃]₄NX, [CH₃(CH₂)₃]₄PX, [CH₃(CH₂)₅]₄NX, [CH₃(CH₂)₆]₄NX, [CH₃(CH₂)₄]₄NX, CH₃[CH₃(CH₂)₃]₃NX, and CH₃[CH₃(CH₂)₂]₃NX wherein X is Cl⁻, Br⁻, a C_1-8 alkoxy group or C_6-188 aryloxy group. An effective amount of a phase transfer catalyst may be about 0.1 to about 10 wt. % based on the weight of bisphenol in the phosgenation mixture. In another embodiment an effective amount of phase transfer catalyst may be about 0.5 to about 2 wt. % based on the weight of bisphenol in the phosgenation mixture.

Alternatively, melt processes may be used. Generally, in the melt polymerization process, polycarbonates may be prepared by co-reacting, in a molten state, the dihydroxy reactant(s) and a diaryl carbonate ester, such as diphenyl carbonate, in the presence of a transesterification catalyst. Volatile monohydric phenol is removed from the molten reactants by distillation and the polymer is isolated as a molten residue.

In one specific embodiment, the polycarbonate is a linear homopolymer derived from bisphenol A, in which each of A¹ and A² is p-phenylene and Y¹ is isopropylidene. The polycarbonates may have an intrinsic viscosity, as determined in chloroform at 25° C., of about 0.3 to about 1.5 deciliters per gram (dl/gm), specifically about 0.45 to about 1.0 dl/gm. The polycarbonates may have a weight average molecular weight of about 10,000 to about 200,000, specifically about 20,000 to about 100,000 as measured by gel permeation chromatography. The polycarbonates are substantially free of impurities, residual acids, residual bases, and/or residual metals that may catalyze the hydrolysis of polycarbonate.

“Polycarbonate” and “polycarbonate resin” as used herein further includes copolymers comprising carbonate chain units together with a different type of chain unit. Such copolymers may be random copolymers, block copolymers, dendrimers and the like. One specific type of copolymer that may be used is a polyester carbonate, also known as a copolyester-polycarbonate. Such copolymers further contain, in addition to recurring carbonate chain units of the formula (1), repeating units of formula (6) wherein E is a divalent radical derived from a dihydroxy compound, and may be, for example, a C_2-10 alkylene radical, a C_6-20 alicyclic radical, a C_6-20 aromatic radical or a polyoxyalkylene radical in which the alkylene groups contain 2 to about 6 carbon atoms, specifically 2, 3, or 4 carbon atoms; and T divalent radical derived from a dicarboxylic acid, and may be, for example, a C_2-10 alkylene radical, a C_6-20 alicyclic radical, a C_6-20 alkyl aromatic radical, or a C_6-20 aromatic radical.

In one embodiment, E is a C_2-6 alkylene radical. In another embodiment, E is derived from an aromatic dihydroxy compound of formula (7): wherein each R^f is independently a halogen atom, a C_1-10 hydrocarbon group, or a C_1-10 halogen substituted hydrocarbon group, and n is 0 to 4. The halogen is preferably bromine. Examples of compounds that may be represented by the formula (7) include resorcinol, substituted resorcinol compounds such as 5-methyl resorcinol, 5-ethyl resorcinol, 5-propyl resorcinol, 5-butyl resorcinol, 5-t-butyl resorcinol, 5-phenyl resorcinol, 5-cumyl resorcinol, 2,4,5,6-tetrafluororesorcinol, 2,4,5,6-tetrabromo resorcinol, and the like; catechol; hydroquinone; substituted hydroquinones such as 2-methyl hydroquinone, 2-ethyl hydroquinone, 2-propyl hydroquinone, 2-butyl hydroquinone, 2-t-butyl hydroquinone, 2-phenyl hydroquinone, 2-cumyl hydroquinone, 2,3,5,6-tetramethyl hydroquinone, 2,3,5,6-tetra-t-butyl hydroquinone, 2,3,5,6-tetrafluorohydroquinone, 2,3,5,6-tetrabromo hydroquinone, and the like; or combinations comprising at least one of the foregoing compounds.

Examples of aromatic dicarboxylic acids that may be used to prepare the polyesters include isophthalic or terephthalic acid, 1,2-di(p-carboxyphenyl)ethane, 4,4′-dicarboxydiphenyl ether, 4,4′-bisbenzoic acid, and mixtures comprising at least one of the foregoing acids. Acids containing fused rings can also be present, such as in 1,4-, 1,5-, or 2,6-naphthalenedicarboxylic acids. Specific dicarboxylic acids are terephtbalic acid, isophthalic acid, naphthalene dicarboxylic acid, cyclohexane dicarboxylic acid, or mixtures thereof. A specific dicarboxylic acid comprises a mixture of isophthalic acid and terephthalic acid wherein the weight ratio of terephthalic acid to isophthalic acid is about 10:1 to about 0.2:9.8. In another specific embodiment, E is a C_2-6 alkylene radical and T is p-phenylene, m-phenylene, naphthalene, a divalent cycloaliphatic radical, or a mixture thereof. This class of polyester includes the poly(alkylene terephthalates).

The copolyester-polycarbonate resins are also prepared by interfacial polymerization. Rather than using the dicarboxylic acid per se, it is possible, and sometimes even preferred, to employ the reactive derivatives of the acid, such as the corresponding acid halides, in particular the acid dichlorides and the acid dibromides. Thus, for example instead of using isophthalic acid, terephthalic acid, and mixtures thereof, it is possible to employ isophthaloyl dichloride, terephthaloyl dichloride, and mixtures thereof. The copolyester-polycarbonate resins may have an intrinsic viscosity, as determined in chloroform at 25° C., of about 0.3 to about 1.5 deciliters per gram (dl/gm), specifically about 0.45 to about 1.0 dl/gm. The copolyester-polycarbonate resins may have a weight average molecular weight of about 10,000 to about 200,000, specifically about 20,000 to about 100,000 as measured by gel permeation chromatography. The copolyester-polycarbonate resins are substantially free of impurities, residual acids, residual bases, and/or residual metals that may catalyze the hydrolysis of polycarbonate.

The polycarbonate component may further comprise, in addition to the polycarbonates described above, combinations of the polycarbonates with other thermoplastic polymers, for example combinations of polycarbonate homopolymers and/or copolymers with polyesters and the like. As used herein, a “combination” is inclusive of all mixtures, blends, alloys, and the like. Suitable polyesters comprise repeating units of formula (6), and may be, for example, poly(alkylene dicarboxylates), liquid crystalline polyesters, and polyester copolymers. It is also possible to use a branched polyester in which a branching agent, for example, a glycol having three or more hydroxyl groups or a trifunctional or multifunctional carboxylic acid has been incorporated. Furthermore, it is sometime desirable to have various concentrations of acid and hydroxyl end groups on the polyester, depending on the ultimate end-use of the composition.

In one embodiment, poly(alkylene terephthalates) are used. Specific examples of suitable poly(alkylene terephthalates) are poly(ethylene terephthalate) (PET), poly(1,4-butylene terephthalate) (PBT), poly(ethylene naphthanoate) (PEN), poly(butylene naphthanoate), (PBN), (polypropylene terephthalate) (PPT), polycyclohexanedimethanol terephthalate (PCT), and combinations comprising at least one of the foregoing polyesters. Also contemplated herein are the above polyesters with a minor amount, e.g., from about 0.5 to about 10 percent by weight, of units derived from an aliphatic diacid and/or an aliphatic polyol to make copolyesters.

The blends of a polycarbonate and a polyester may comprise about 10 to about 99 wt. % polycarbonate and correspondingly about 1 to about 90 wt. % polyester, in particular a poly(alkylene terephthalate). In one embodiment, the blend comprises about 30 to about 70 wt. % polycarbonate and correspondingly about 30 to about 70 wt. % polyester. The foregoing amounts are based on the combined weight of the polycarbonate and polyester.

Although blends of polycarbonates with other polymers are contemplated, in one embodiment the polycarbonate component consists essentially of polycarbonate, i.e., the polycarbonate component comprises polycarbonate homopolymers and/or polycarbonate copolymers, and no other resins that would significantly adversely impact the hydrolytic stability, thermal stability, and/or impact strength of the thermoplastic composition. In another embodiment, the polycarbonate component consists of polycarbonate, i.e., is composed of only polycarbonate homopolymers and/or polycarbonate copolymers.

The thermoplastic composition further includes an impact modifier. One type of impact modifier suitable for use in the invention is a bulk polymerized ABS. The bulk polymerized ABS comprises an elastomeric phase comprising (i) butadiene and having a Tg of less than about 10° C., and (ii) a rigid polymeric phase having a Tg of greater than about 15° C. and comprising a copolymer of a monovinylaromatic monomer such as styrene and an unsaturated nitrile such as acrylonitrile. Such ABS polymers may be prepared by first providing the elastomeric polymer, then polymerizing the constituent monomers of the rigid phase in the presence of the elastomer to obtain the graft copolymer. The grafts may be attached as graft branches or as shells to an elastomer core. The shell may merely physically encapsulate the core, or the shell may be partially or essentially completely grafted to the core.

Polybutadiene homopolymer may be used as the elastomer phase. Alternatively, the elastomer phase of the bulk polymerized ABS comprises butadiene copolymerized with up to about 25 wt. % of another conjugated diene monomer of formula (8): wherein each X^b is independently C₁-C₅ alkyl. Examples of conjugated diene monomers that may be used are isoprene, 1,3-heptadiene, methyl-1,3-pentadiene, 2,3-dimethyl-1,3-butadiene, 2-ethyl-1,3-pentadiene; 1,3- and 2,4-hexadienes, and the like, as well as mixtures comprising at least one of the foregoing conjugated diene monomers. A specific conjugated diene is isoprene.

The elastomeric butadiene phase may additionally be copolymerized with up to 25 wt %, specifically up to about 15 wt. %, of another comonomer, for example monovinylaromatic monomers containing condensed aromatic ring structures such as vinyl naphthalene, vinyl anthracene and the like, or monomers of formula (9): wherein each X^c is independently hydrogen, C₁-C₁₂ alkyl, C₃-C₁₂ cycloalkyl, C₆-C₁₂ aryl, C₇-C₁₂ aralkyl, C₇-C₁₂ alkaryl, C₁-C₁₂ alkoxy, C₃-C₁₂ cycloalkoxy, C₆-C1₁₂ aryloxy, chloro, bromo, or hydroxy, and R is hydrogen, C₁-C₅ alkyl, bromo, or chloro. Examples of suitable monovinylaromatic monomers copolymerizable with the butadiene include styrene, 3-methylstyrene, 3,5-diethylstyrene, 4-n-propylstyrene, alpha-methylstyrene, alpha-methyl vinyltoluene, alpha-chlorostyrene, alpha-bromostyrene, dichlorostyrene, dibromostyrene, tetra-chlorostyrene, and the like, and combinations comprising at least one of the foregoing monovinylaromatic monomers. In one embodiment, the butadiene is copolymerized with up to about 12 wt. %, specifically about 1 to about 10 wt. % styrene and/or alpha-methyl styrene.

Other monomers that may be copolymerized with the butadiene are monovinylic monomers such as itaconic acid, acrylamide, N-substituted acrylamide or methacrylamide, maleic anhydride, maleimide, N-alkyl-, aryl-, or haloaryl-substituted maleimide, glycidyl (meth)acrylates, and monomers of the generic formula (10): wherein R is hydrogen, C₁-C₅ alkyl, bromo, or chloro, and X^c is cyano, C₁-C₁₂ alkoxycarbonyl, C₁-C₁₂ aryloxycarbonyl, hydroxy carbonyl, and the like. Examples of monomers of formula (10) include acrylonitrile, ethacrylonitrile, methacrylonitrile, alpha-chloroacrylonitrile, beta-chloroacrylonitrile, alpha-bromoacrylonitrile, acrylic acid, methyl (meth)acrylate, ethyl (meth)acrylate, n-butyl (meth)acrylate, t-butyl (meth)acrylate, n-propyl (meth)acrylate, isopropyl (meth)acrylate, 2-ethylhexyl (meth)acrylate, and the like, and combinations comprising at least one of the foregoing monomers. Monomers such as n-butyl acrylate, ethyl acrylate, and 2-ethylhexyl acrylate are commonly used as monomers copolymerizable with the butadiene.

The particle size of the butadiene phase is not critical, and may be, for example about 0.01 to about 20 micrometers, specifically about 0.5 to about 10 micrometers, more specifically about 0.6 to about 1.5 micrometers may be used for bulk polymerized rubber substrates. Particle size may be measured by light transmission methods or capillary hydrodynamic chromatography (CHDF). The butadiene phase may provide about 5 to about 95 wt. % of the total weight of the ABS impact modifier copolymer, more specifically about 20 to about 90 wt. %, and even more specifically about 40 to about 85 wt. % of the ABS impact modifier, the remainder being the rigid graft phase.

The rigid graft phase comprises a copolymer formed from a styrenic monomer composition together with an unsaturated monomer comprising a nitrile group. As used herein, “styrenic monomer” includes monomers of formula (9) wherein each X^c is independently hydrogen, C₁-C₄ alkyl, phenyl, C₇-C₉ aralkyl, C₇-C₉ alkaryl, C₁-C₄ alkoxy, phenoxy, chloro, bromo, or hydroxy, and R is hydrogen, C₁-C₂ alkyl, bromo, or chloro. Specific examples styrene, 3-methylstyrene, 3,5-diethylstyrene, 4-n-propylstyrene, alpha-methylstyrene, alpha-methyl vinyltoluene, alpha-chlorostyrene, alpha-bromostyrene, dichlorostyrene, dibromostyrene, tetra-chlorostyrene, and the like. Combinations comprising at least one of the foregoing styrenic monomers may be used.

Further as used herein, an unsaturated monomer comprising a nitrile group includes monomers of formula (10) wherein R is hydrogen, C₁-C₅ alkyl, bromo, or chloro, and X^c is cyano. Specific examples include acrylonitrile, ethacrylonitrile, methacrylonitrile, alpha-chloroacrylonitrile, beta-chloroacrylonitrile, alpha-bromoacrylonitrile, and the like. Combinations comprising at least one of the foregoing monomers may be used.

The rigid graft phase of the bulk polymerized ABS may further optionally comprise other monomers copolymerizable therewith, including other monovinylaromatic monomers and/or monovinylic monomers such as itaconic acid, acrylamide, N-substituted acrylamide or methacrylamide, maleic anhydride, maleimide, N-alkyl-, aryl-, or haloaryl-substituted maleimide, glycidyl (meth)acrylates, and monomers of the generic formula (10). Specific comonomers include C₁-C₄ alkyl (meth)acrylates, for example methyl methacrylate.

The rigid copolymer phase will generally comprise about 10 to about 99 wt. %, specifically about 40 to about 95 wt. %, more specifically about 50 to about 90 wt. % of the styrenic monomer; about 1 to about 90 wt. %, specifically about 10 to about 80 wt. %, more specifically about 10 to about 50 wt. % of the unsaturated monomer comprising a nitrile group; and 0 to about 25 wt. %, specifically 1 to about 15 wt. % of other comonomer, each based on the total weight of the rigid copolymer phase.

The bulk polymerized ABS copolymer may further comprise a separate matrix or continuous phase of ungrafted rigid copolymer that may be simultaneously obtained with the ABS. The ABS may comprise about 40 to about 95 wt. % elastomer-modified graft copolymer and about 5 to about 65 wt. % rigid copolymer, based on the total weight of the ABS. In another embodiment, the ABS may comprise about 50 to about 85 wt. %, more specifically about 75 to about 85 wt. % elastomer-modified graft copolymer, together with about 15 to about 50 wt. %, more specifically about 15 to about 25 wt. % rigid copolymer, based on the total weight of the ABS.

A variety of bulk polymerization methods for ABS-type resins are known. In multizone plug flow bulk processes, a series of polymerization vessels (or towers), consecutively connected to each other, providing multiple reaction zones. The elastomeric butadiene may be dissolved in one or more of the monomers used to form the rigid phase, and the elastomer solution is fed into the reaction system. During the reaction, which may be thermally or chemically initiated, the elastomer is grafted with the rigid copolymer (i.e., SAN). Bulk copolymer (referred to also as free copolymer, matrix copolymer, or non-grafted copolymer) is also formed within the continuous phase containing the dissolved rubber. As polymerization continues, domains of free copolymer are formed within the continuous phase of rubber/comonomers to provide a two-phase system. As polymerization proceeds, and more free copolymer is formed, the elastomer-modified copolymer starts to disperse itself as particles in the free copolymer and the free copolymer becomes a continuous phase (phase inversion). Some free copolymer is generally occluded within the elastomer-modified copolymer phase as well. Following the phase inversion, additional heating may be used to complete polymerization. Numerous modifications of this basis process have been described, for example in U.S. Pat. No. 3,511,895, which describes a continuous bulk ABS process that provides controllable molecular weight distribution and microgel particle size using a three-stage reactor system. In the first reactor, the elastomer/monomer solution is charged into the reaction mixture under high agitation to precipitate discrete rubber particle uniformly throughout the reactor mass before appreciable cross-linking can occur. Solids levels of the first, the second, and the third reactor are carefully controlled so that molecular weights fall into a desirable range. U.S. Pat. No. 3,981,944 discloses extraction of the elastomer particles using the styrenic monomer to dissolve/disperse the elastomer particles, prior to addition of the unsaturated monomer comprising a nitrile group and any other comonomers. U.S. Pat. No. 5,414,045 discloses reacting in a plug flow grafting reactor a liquid feed composition comprising a styrenic monomer composition, an unsaturated nitrile monomer composition, and an elastomeric butadiene polymer to a point prior to phase inversion, and reacting the first polymerization product (grafted elastomer) therefrom in a continuous-stirred tank reactor to yield a phase inverted second polymerization product that then can be further reacted in a finishing reactor, and then devolatilized to produce the desired final product.

In addition to the bulk polymerized ABS, other impact modifiers may be used in the thermoplastic composition. These impact modifiers include elastomer-modified graft copolymers comprising (i) an elastomeric (i.e., rubbery) polymer substrate having a Tg less than about 10° C., more specifically less than about −10° C., or more specifically about −40° to −80° C., and (ii) a rigid polymeric superstrate grafted to the elastomeric polymer substrate. The grafts may be attached as graft branches or as shells to an elastomer core. The shell may merely physically encapsulate the core, or the shell may be partially or essentially completely grafted to the core.

Suitable materials for use as the elastomer phase include, for example, conjugated diene rubbers; copolymers of a conjugated diene with less than about 50 wt. % of a copolymerizable monomer; olefin rubbers such as ethylene propylene copolymers (EPR) or ethylene-propylene-diene monomer rubbers (EPDM); ethylene-vinyl acetate rubbers; silicone rubbers; elastomeric C_1-8 alkyl (meth)acrylates; elastomeric copolymers of C_1-8 alkyl (meth)acrylates with butadiene and/or styrene; or combinations comprising at least one of the foregoing elastomers.

Suitable conjugated diene monomers for preparing the elastomer phase are of formula (8) above wherein each X^b is independently hydrogen, C₁-C₅ alkyl, and the like. Examples of conjugated diene monomers that may be used are butadiene, isoprene, 1,3-heptadiene, methyl-1,3-pentadiene, 2,3-dimethyl-1,3-butadiene, 2-ethyl-1,3-pentadiene; 1,3- and 2,4-hexadienes, and the like, as well as mixtures comprising at least one of the foregoing conjugated diene monomers. Specific conjugated diene homopolymers include polybutadiene and polyisoprene.

Copolymers of a conjugated diene rubber may also be used, for example those produced by aqueous radical emulsion polymerization of a conjugated diene and one or more monomers copolymerizable therewith. Monomers that are suitable for copolymerization with the conjugated diene include monovinylaromatic monomers containing condensed aromatic ring structures, such as vinyl naphthalene, vinyl anthracene and the like, or monomers of formula (9) above, wherein each X^c is independently hydrogen, C₁-C₁₂ alkyl, C₃-C₁₂ cycloalkyl, C₆-C₁₂ aryl, C₇-C₁₂ aralkyl, C₇-C₁₂ alkaryl, C₁-C₁₂ alkoxy, C₃-C₁₂ cycloalkoxy, C₆-C₁₂ aryloxy, chloro, bromo, or hydroxy, and R is hydrogen, C₁-C₅ alkyl, bromo, or chloro. Examples of suitable monovinylaromatic monomers that may be used include styrene, 3-methylstyrene, 3,5-diethylstyrene, 4-n-propylstyrene, alpha-methylstyrene, alpha-methyl vinyltoluene, alpha-chlorostyrene, alpha-bromostyrene, dichlorostyrene, dibromostyrene, tetra-chlorostyrene, combinations comprising at least one of the foregoing compounds, and the like. Styrene and/or alpha-methylstyrene are commonly used as monomers copolymerizable with the conjugated diene monomer.

Other monomers that may be copolymerized with the conjugated diene are monovinylic monomers such as itaconic acid, acrylamide, N-substituted acrylamide or methacrylamide, maleic anhydride, maleimide, N-alkyl-, aryl-, or haloaryl-substituted maleimide, glycidyl (meth)acrylates, and monomers of the generic formula (10) wherein R is hydrogen, C₁-C₅ alkyl, bromo, or chloro, and X^c is cyano, C₁-C₁₂ alkoxycarbonyl, C₁-C₁₂ aryloxycarbonyl, hydroxy carbonyl, and the like. Examples of monomers of formula (10) include acrylonitrile, ethacrylonitrile, methacrylonitrile, alpha-chloroacrylonitrile, beta-chloroacrylonitrile, alpha-bromoacrylonitrile, acrylic acid, methyl (meth)acrylate, ethyl (meth)acrylate, n-butyl (meth)acrylate, t-butyl (meth)acrylate, n-propyl (meth)acrylate, isopropyl (meth)acrylate, 2-ethylhexyl (meth)acrylate, and the like, and combinations comprising at least one of the foregoing monomers. Monomers such as n-butyl acrylate, ethyl acrylate, and 2-ethylhexyl acrylate are commonly used as monomers copolymerizable with the conjugated diene monomer. Mixtures of the foregoing monovinyl monomers and monovinylaromatic monomers may also be used.

Certain (meth)acrylate monomers may also be used to provide the elastomer phase, including cross-linked, particulate emulsion homopolymers or copolymers of C_1-16 alkyl (meth)acrylates, specifically C_1-9 alkyl (meth)acrylates, in particular C_4-6 alkyl acrylates, for example n-butyl acrylate, t-butyl acrylate, n-propyl acrylate, isopropyl acrylate, 2-ethylhexyl acrylate, and the like, and combinations comprising at least one of the foregoing monomers. The C_1-16 alkyl (meth)acrylate monomers may optionally be polymerized in admixture with up to 15 wt. % of comonomers of generic formulas (8), (9), or (10) as broadly described above. Exemplary comonomers include but are not limited to butadiene, isoprene, styrene, methyl methacrylate, phenyl methacrylate, phenethylmethacrylate, N-cyclohexylacrylamide, vinyl methyl ether or acrylonitrile, and mixtures comprising at least one of the foregoing comonomers. Optionally, up to 5 wt. % a polyfunctional crosslinking comonomer may be present, for example divinylbenzene, alkylenediol di(meth)acrylates such as glycol bisacrylate, alkylenetriol tri(meth)acrylates, polyester di(meth)acrylates, bisacrylamides, triallyl cyanurate, triallyl isocyanurate, allyl (meth)acrylate, diallyl maleate, diallyl fumarate, diallyl adipate, triallyl esters of citric acid, triallyl esters of phosphoric acid, and the like, as well as combinations comprising at least one of the foregoing crosslinking agents.

The elastomer phase may be polymerized by mass, emulsion, suspension, solution or combined processes such as bulk-suspension, emulsion-bulk, bulk-solution or other techniques, using continuous, semibatch, or batch processes. The particle size of the elastomer substrate is not critical. For example, an average particle size of about 0.001 to about 25 micrometers, specifically about 0.01 to about 15 micrometers, or even more specifically about 0.1 to about 8 micrometers may be used for emulsion based polymerized rubber lattices. A particle size of about 0.5 to about 10 micrometers, specifically about 0.6 to about 1.5 micrometers may be used for bulk polymerized rubber substrates. The elastomer phase may be a particulate, moderately cross-linked copolymer derived from conjugated butadiene or C_4-9 alkyl acrylate rubber, and preferably has a gel content greater than 70%. Also suitable are copolymers derived from mixtures of butadiene with styrene, acrylonitrile, and/or C_4-6 alkyl acrylate rubbers.

The elastomeric phase may provide about 5 to about 95 wt. % of the elastomer-modified graft copolymer, more specifically about 20 to about 90 wt. %, and even more specifically about 40 to about 85 wt. %, the remainder being the rigid graft phase.

The rigid phase of the elastomer-modified graft copolymer may be formed by graft polymerization of a mixture comprising a monovinylaromatic monomer and optionally one or more comonomers in the presence of one or more elastomeric polymer substrates. The above broadly described monovinylaromatic monomers of formula (9) may be used in the rigid graft phase, including styrene, alpha-methyl styrene, halostyrenes such as dibromostyrene, vinyltoluene, vinylxylene, butylstyrene, para-hydroxystyrene, methoxystyrene, and the like, or combinations comprising at least one of the foregoing monovinylaromatic monomers. Suitable comonomers include, for example, the above broadly described monovinylic monomers and/or monomers of the general formula (10). In one embodiment, R is hydrogen or C₁-C₂ alkyl, and X^c is cyano or C₁-C₁₂ alkoxycarbonyl. Specific examples of suitable comonomers for use in the rigid phase include acrylonitrile, ethacrylonitrile, methacrylonitrile, methyl (meth)acrylate, ethyl (meth)acrylate, n-propyl (meth)acrylate, isopropyl (meth)acrylate, and the like, and combinations comprising at least one of the foregoing comonomers.

In one specific embodiment, the rigid graft phase is formed from styrene or alpha-methyl styrene copolymerized with ethyl acrylate and/or methyl methacrylate. In other specific embodiments, the rigid graft phase is formed from styrene copolymerized with; styrene copolymerized with methyl methacrylate; and styrene copolymerized with methyl methacrylate and acrylonitrile.

The relative ratio of monovinylaromatic monomer and comonomer in the rigid graft phase may vary widely depending on the type of elastomer substrate, type of monovinylaromatic monomer(s), type of comonomer(s), and the desired properties of the impact modifier. The rigid phase may generally comprise up to 100 wt. % of monovinyl aromatic monomer, specifically about 30 to about 100 wt. %, more specifically about 50 to about 90 wt. % monovinylaromatic monomer, with the balance being comonomer(s).

Depending on the amount of elastomer-modified polymer present, a separate matrix or continuous phase of ungrafted rigid polymer or copolymer may be simultaneously obtained along with the additional elastomer-modified graft copolymer. Typically, such impact modifiers comprise about 40 to about 95 wt. % elastomer-modified graft copolymer and about 5 to about 65 wt. % rigid (co)polymer, based on the total weight of the impact modifier. In another embodiment, such impact modifiers comprise about 50 to about 85 wt. %, more specifically about 75 to about 85 wt. % rubber-modified rigid copolymer, together with about 15 to about 50 wt. %, more specifically about 15 to about 25 wt. % rigid (co)polymer, based on the total weight of the impact modifier.

Specific examples of elastomer-modified graft copolymers that differ from the bulk polymerized ABS include but are not limited to acrylonitrile-styrene-butyl acrylate (ASA), methyl methacrylate-acrylonitrile-butadiene-styrene (MABS),methyl methacrylate-butadiene-styrene (MBS), and acrylonitrile-ethylene-propylene-diene-styrene (AES). The MBS resins may be prepared by emulsion polymerization of methacrylate and styrene in the presence of polybutadiene as is described in U.S. Pat. No. 6,545,089, which process is summarized below.

Another specific type of elastomer-modified impact modifier comprises structural units derived from at least one silicone rubber monomer, a branched acrylate rubber monomer having the formula H₂C═C(R^d)C(O)OCH₂CH₂R^e, wherein R^d is hydrogen or a C₁-C₉ linear or branched hydrocarbyl group and R^e is a branched C₃-C₁₆ hydrocarbyl group; a first graft link monomer; a polymerizable alkenyl-containing organic material; and a second graft link monomer. The silicone rubber monomer may comprise, for example, a cyclic siloxane, tetraalkoxysilane, trialkoxysilane, (acryloxy)alkoxysilane, (mercaptoalkyl)alkoxysilane, vinylalkoxysilane, or allylalkoxysilane, alone or in combination, e.g., decamethylcyclopentasiloxane, dodecamethylcyclohexasiloxane, trimethyltriphenylcyclotrisiloxane, tetramethyltetraphenylcyclotetrasiloxane, tetramethyltetravinylcyclotetrasiloxane, octaphenylcyclotetrasiloxane, octamethylcyclotetrasiloxane and/or tetraethoxysilane.

Exemplary branched acrylate rubber monomers include iso-octyl acrylate, 6-methyloctyl acrylate, 7-methyloctyl acrylate, 6-methylheptyl acrylate, and the like, alone or in combination. The polymerizable alkenyl-containing organic material may be, for example, a monomer of formula (9) or (10), e.g., styrene, alpha-methylstyrene, acrylonitrile, methacrylonitrile, or an unbranched (meth)acrylate such as methyl methacrylate, 2-ethylhexyl methacrylate, methyl acrylate, ethyl acrylate, n-propyl acrylate, and the like, alone or in combination.

The at least one first graft link monomer may be an (acryloxy)alkoxysilane, a (mercaptoalkyl)alkoxysilane, a vinylalkoxysilane, or an allylalkoxysilane, alone or in combination, e.g., (gamma-methacryloxypropyl)(dimethoxy)methylsilane and/or (3-mercaptopropyl)trimethoxysilane. The at least one second graft link monomer is a polyethylenically unsaturated compound having at least one allyl group, such as allyl methacrylate, triallyl cyanurate, or triallyl isocyanurate, alone or in combination.

The silicone-acrylate impact modifier compositions can be prepared by emulsion polymerization, wherein, for example at least one silicone rubber monomer is reacted with at least one first graft link monomer at a temperature from about 30° C. to about 110° C. to form a silicone rubber latex, in the presence of a surfactant such as dodecylbenzenesulfonic acid. Alternatively, a cyclic siloxane such as cyclooctamethyltetrasiloxane and an tetraethoxyorthosilicate may be reacted with a first graft link monomer such as (gamma-methacryloxypropyl)methyldimethoxysilane, to afford silicone rubber having an average particle size from about 100 nanometers to about 2 microns. At least one branched acrylate rubber monomer is then polymerized with the silicone rubber particles, optionally in presence of a cross linking monomer, such as allylmethacrylate in the presence of a free radical generating polymerization catalyst such as benzoyl peroxide. This latex is then reacted with a polymerizable alkenyl-containing organic material and a second graft link monomer. The latex particles of the graft silicone-acrylate rubber hybrid may be separated from the aqueous phase through coagulation (by treatment with a coagulant) and dried to a fine powder to produce the silicone-acrylate rubber impact modifier composition. This method can be generally used for producing the silicone-acrylate impact modifier having a particle size from about 100 nanometers to about two micrometers.

In practice, any of the above described impact modifiers, or combinations of one or more of the foregoing impact modifiers, may be used. Processes for the formation of the elastomer-modified graft copolymers include mass, emulsion, suspension, and solution processes, or combined processes such as bulk-suspension, emulsion-bulk, bulk-solution or other techniques, using continuous, semibatch, or batch processes. Such processes may be conducted so as to avoid the use or production of any species that degrade polycarbonates, if desired, and/or to provide the additional impact modifiers with the desired pH.

In one embodiment, the impact modifier is prepared by an emulsion polymerization process that avoids the use or production of any species that degrade polycarbonates. In another embodiment the impact modifier is prepared by an emulsion polymerization process that is free of basic species, for example species such as alkali metal salts of C_6-30 fatty acids, for example sodium stearate, lithium stearate, sodium oleate, potassium oleate, and the like, alkali metal carbonates, amines such as dodecyl dimethyl amine, dodecyl amine, and the like, and ammonium salts of amines. Such materials are commonly used as polymerization aids, e.g., surfactants in emulsion polymerization, and may catalyze transesterification and/or degradation of polycarbonates. Instead, ionic sulfate, sulfonate or phosphate surfactants may be used in preparing the impact modifiers, particularly the elastomeric substrate portion of the impact modifiers. Suitable surfactants include, for example, C_1-22 alkyl or C_7-25 alkylaryl sulfonates, C_1-22 alkyl or C_7-25 alkylaryl sulfates, C_1-22 alkyl or C_7-25 alkylaryl phosphates, substituted silicates, and combinations comprising at least one of the foregoing surfactants. A specific surfactant is a C_6-16, specifically a C_8-12 alkyl sulfonate. This emulsion polymerization process is described and disclosed in various patents and literature of such companies as Rohm & Haas and General Electric Company.

The composition optionally comprises a polycarbonate-polysiloxane copolymer comprising polycarbonate blocks and polydiorganosiloxane blocks. The polycarbonate blocks in the copolymer comprise repeating structural units of formula (1) as described above, for example wherein R¹ is of formula (2) as described above. These units may be derived from reaction of dihydroxy compounds of formula (3) as described above. In one embodiment, the dihydroxy compound is bisphenol A, in which each of A¹ and A² is p-phenylene and Y¹ is isopropylidene.

The polydiorganosiloxane blocks comprise repeating structural units of formula (11) (sometimes referred to herein as ‘siloxane’): wherein each occurrence of R is same or different, and is a C_1-13 monovalent organic radical. For example, R may be a C₁-C₁₃ alkyl group, C₁-C₁₃ alkoxy group, C₂-C₁₃ alkenyl group, C₂-C₁₃ alkenyloxy group, C₃-C₆ cycloalkyl group, C₃-C₆ cycloalkoxy group, C₆-C₁₀ aryl group, C₆-C₁₀ aryloxy group, C₇-C₁₃ aralkyl group, C₇-C₁₃ aralkoxy group, C₇-C₁₃ alkaryl group, or C₇-C₁₃ alkaryloxy group. Combinations of the foregoing R groups may be used in the same copolymer.

The value of D in formula (11) may vary widely depending on the type and relative amount of each component in the thermoplastic composition, the desired properties of the composition, and like considerations. Generally, D may have an average value of 2 to about 1000, specifically about 2 to about 500, more specifically about 5 to about 100. In one embodiment, D has an average value of about 10 to about 75, and in still another embodiment, D has an average value of about 40 to about 60. Where D is of a lower value, e.g., less than about 40, it may be desirable to use a relatively larger amount of the polycarbonate-polysiloxane copolymer. Conversely, where D is of a higher value, e.g., greater than about 40, it may be necessary to use a relatively lower amount of the polycarbonate-polysiloxane copolymer.

A combination of a first and a second (or more) polycarbonate-polysiloxane copolymers may be used, wherein the average value of D of the first copolymer is less than the average value of D of the second copolymer.

In one embodiment, the polydiorganosiloxane blocks are provided by repeating structural units of formula (12): wherein D is as defined above; each R may be the same or different, and is as defined above; and Ar may be the same or different, and is a substituted or unsubstituted C₆-C₃₀ arylene radical, wherein the bonds are directly connected to an aromatic moiety. Suitable Ar groups in formula (12) may be derived from a C₆-C₃₀ dihydroxyarylene compound, for example a dihydroxyarylene compound of formula (3), (4), or (7) above. Combinations comprising at least one of the foregoing dihydroxyarylene compounds may also be used. Specific examples of suitable dihydroxyarylene compounds are 1,1-bis(4-hydroxyphenyl) methane, 1,1-bis(4-hydroxyphenyl) ethane, 2,2-bis(4-hydroxyphenyl) propane, 2,2-bis(4-hydroxyphenyl) butane, 2,2-bis(4-hydroxyphenyl) octane, 1,1-bis(4-hydroxyphenyl) propane, 1,1-bis(4-hydroxyphenyl) n-butane, 2,2-bis(4-hydroxy-1-methylphenyl) propane, 1,1-bis(4-hydroxyphenyl) cyclohexane, bis(4-hydroxyphenyl sulphide), and 1,1-bis(4-hydroxy-t-butylphenyl) propane. Combinations comprising at least one of the foregoing dihydroxy compounds may also be used.

Such units may be derived from the corresponding dihydroxy compound of the following formula:

wherein Ar and D are as described above. Such compounds are further described in U.S. Pat. No. 4,746,701 to Kress et al. Compounds of this formula may be obtained by the reaction of a dihydroxyarylene compound with, for example, an alpha, omega-bisacetoxypolydiorangonosiloxane under phase transfer conditions.

In another embodiment the polydiorganosiloxane blocks comprise repeating structural units of formula (13)

wherein R and D are as defined above. R² in formula (13) is a divalent C₂-C₈ aliphatic group. Each M in formula (13) may be the same or different, and may be a halogen, cyano, nitro, C₁-C₈ alkylthio, C₁-C₈ alkyl, C₁-C₈ alkoxy, C₂-C₈ alkenyl, C₂-C₈ alkenyloxy group, C₃-C₈ cycloalkyl, C₃-C₈ cycloalkoxy, C₆-C₁₀ aryl, C₆-C₁₀ aryloxy, C₇-C₁₂ aralkyl, C₇-C₁₂ aralkoxy, C₇-C₁₂ alkaryl, or C₇-C₁₂ alkaryloxy, wherein each n is independently 0, 1, 2, 3, or 4.

In one embodiment, M is bromo or chloro, an alkyl group such as methyl, ethyl, or propyl, an alkoxy group such as methoxy, ethoxy, or propoxy, or an aryl group such as phenyl, chlorophenyl, or tolyl; R² is a dimethylene, trimethylene or tetramethylene group; and R is a C_1-8 alkyl, haloalkyl such as trifluoropropyl, cyanoalkyl, or aryl such as phenyl, chlorophenyl or tolyl. In another embodiment, R is methyl, or a mixture of methyl and trifluoropropyl, or a mixture of methyl and phenyl. In still another embodiment, M is methoxy, n is one, R² is a divalent C₁-C₃ aliphatic group, and R is methyl.

These units may be derived from the corresponding dihydroxy polydiorganosiloxane (14): wherein R, D, M, R², and n are as described above.

Such dihydroxy polysiloxanes can be made by effecting a platinum catalyzed addition between a siloxane hydride of the formula (15), wherein R and D are as previously defined, and an aliphatically unsaturated monohydric phenol. Suitable aliphatically unsaturated monohydric phenols included, for example, eugenol, 2-alkylphenol, 4-allyl-2-methylphenol, 4-allyl-2-phenylphenol, 4-allyl-2-bromophenol, 4-allyl-2-t-butoxyphenol, 4-phenyl-2-phenylphenol, 2-methyl-4-propylphenol, 2-allyl-4,6-dimethylphenol, 2-allyl-4-bromo-6-methylphenol, 2-allyl-6-methoxy-4-methylphenol and 2-allyl-4,6-dimethylphenol. Mixtures comprising at least one of the foregoing may also be used.

The polycarbonate-polysiloxane copolymer may be manufactured by reaction of diphenolic polysiloxane (14) with a carbonate source and a dihydroxy aromatic compound of formula (3), optionally in the presence of a phase transfer catalyst as described above. Suitable conditions are similar to those useful in forming polycarbonates. For example, the copolymers are prepared by phosgenation, at temperatures from below 0° C. to about 100° C., preferably about 25° C. to about 50° C. Since the reaction is exothermic, the rate of phosgene addition may be used to control the reaction temperature. The amount of phosgene required will generally depend upon the amount of the dihydric reactants. Alternatively, the polycarbonate-polysiloxane copolymers may be prepared by co-reacting in a molten state, the dihydroxy monomers and a diaryl carbonate ester, such as diphenyl carbonate, in the presence of a transesterification catalyst as described above.

In the production of the polycarbonate-polysiloxane copolymer, the amount of dihydroxy polydiorganosiloxane is selected so as to provide the desired amount of polydiorganosiloxane units in the copolymer. The amount of polydiorganosiloxane units may vary widely, that is, may be about 1 wt. % to about 99 wt. % of polydimethylsiloxane, or an equivalent molar amount of another polydiorganosiloxane, with the balance being carbonate units. The particular amounts used will therefore be determined depending on desired physical properties of the thermoplastic composition, the value of D (within the range of 2 to about 1000), and the type and relative amount of each component in the thermoplastic composition, including the type and amount of polycarbonate, type and amount of impact modifier, type and amount of polycarbonate-polysiloxane copolymer, and type and amount of any other additives. Suitable amounts of dihydroxy polydiorganosiloxane can be determined by one of ordinary skill in the art without undue experimentation using the guidelines taught herein. For example, the amount of dihydroxy polydiorganosiloxane may be selected so as to produce a copolymer comprising about 1 wt. % to about 75 wt. %, or about 1 wt. % to about 50 wt. % polydimethylsiloxane, or an equivalent molar amount of another polydiorganosiloxane. In one embodiment, the copolymer comprises about 5 wt. % to about 40 wt. %, optionally about 5 wt. % to about 25 wt. % polydimethylsiloxane, or an equivalent molar amount of another polydiorganosiloxane, with the balance being polycarbonate. In a particular embodiment, the copolymer may comprise about 20 wt. % siloxane.

The polycarbonate-polysiloxane copolymers have a weight-average molecular weight (MW, measured, for example, by gel permeation chromatography, ultra-centrifugation, or light scattering) of about 10,000 g/mol to about 200,000 g/mol, specifically about 20,000 g/mol to about 100,000 g/mol.

The thermoplastic composition further comprises a particular type of aliphatic/aromatic co-polycarbonate. In one embodiment, the aliphatic/aromatic co-polycarbonate is prepared by reacting a dihydroxy aromatic compound under interfacial conditions with phosgene and an aliphatic chloroformate, wherein the aliphatic chloroformate is prepared by a method comprising introducing a mixture of at least one functional aliphatic compound, phosgene, a solvent, and optionally at least one organic base into a flow reactor to obtain a unidirectional flowing reaction mixture. The co-polycarbonate may be made according to the method described in copending application Ser. No. 10/968,773, filed Oct. 19, 2004.

The term “functional aliphatic compound” as used herein refers to an organic species comprising at least one functional group attached to a non-aromatic carbon atom. A functional group attached to a non-aromatic carbon atom is referred to herein as a “functional aliphatic group”. The functional group may be a hydroxyl, carboxyl, ester or acid chloride group. Examples of aliphatic hydroxyl compounds include, but are not limited to, methanol, ethanol, ethylene glycol, cyclohexanol, sucrose, dextrose, benzyl alcohol, and cholesterol. Conversely, organic species which do not comprise a functional group attached to a non-aromatic carbon atom are not ranked among functional aliphatic compounds. Phenol, hydroquinone, beta-naphthol; 1,3,5-trihydroxybenzene; and 3-hydroxypyridine exemplify organic species comprising one or more hydroxyl groups which do not qualify as functionalized aliphatic compounds, or specifically functionalized aliphatic hydroxyl compounds. However, compounds comprising functional groups attached to both aromatic- and non-aromatic carbon atoms, for example 4-hydroxybenzyl alcohol, fall within the group defined by the term functional aliphatic compounds.

Functionalized aliphatic compounds suitable for use according to the present invention include functionalized aliphatic compounds having at least one functional aliphatic group, such as a hydroxyl group. In one embodiment, the functional aliphatic compound comprises formula (16) X—R—X   (16)

wherein R is a C₁-C₁₈ aliphatic radical, a C₃-C₁₈ cycloaliphatic radical, and each X is independently a hydroxyl, carboxyl, ester or acid chloride group selected from the following formulas: —OH; —R²OH; —COOH; —COOR²; and —COCl

wherein each R² is independently a C₁-C₁₈ monovalent hydrocarbon. For example, when if each X is an —OH group and R is (CH₂)₂, the compound defined by formula (16) is ethylene glycol (HO(CH₂)₂)OH). As a further example, if R is (CH₂)₄ and each X is an —OH group, the compound defined by formula (16) is 1,4-butanediol (HO(CH₂)₄)OH), or if R is C(CH₃)₂, and each X is —R²OH wherein R² is CH₂, the compound defined by formula (16) is neopentyl glycol (CH₃)₂C(CH₂OH)₂).

Examples of suitable functional aliphatic compounds include aliphatic diols and aliphatic polyols. In certain embodiments the functional aliphatic compound may also be selected from the group consisting of polymeric aliphatic hydroxy compounds. Polymeric aliphatic hydroxy compounds include oligomeric species, defined herein as having a weight average molecular weight (M_w) of less than or equal to 15000 grams per mole as measured by gel permeation chromatography using polystyrene molecular weight standards. Polymeric aliphatic hydroxy compounds also include high molecular weight species oligomeric species, defined herein as having a weight average molecular weight (M_w) of greater than 15000 grams per mole as measured by gel permeation chromatography using polystyrene molecular weight standards. Exemplary aliphatic hydroxy compounds include, but are not limited to, neopentyl glycol, 1-hexanol, polyethylene glycol, polytetrahydrofuran diol, polypropylene oxide diol, poly(ethylene-butylene)copolymer diols, trimethylolpropane, isosorbide, cholesterol, menthol, 3-pentanol, tertiary-amyl alcohol, allyl alcohol, propargyl alcohol, ethylene glycol, 1,6-hexanediol and 1,4-butanediol.

The aliphatic/aromatic co-polycarbonate has in addition to repeating carbonate chain units of formula (1), repeating units of the functional aliphatic compound of formula (16). The repeating units of formula (16) are present an amount of from about 2 to about 30 mole percent. Illustrative examples of compounds suitable for use as the carbonate units of formula (1) include 1,1-bis(4-hydroxyphenyl) methane, 1,1-bis(4-hydroxyphenyl) ethane, 2,2-bis(4-hydroxyphenyl) propane (hereinafter “bisphenol A” or “BPA”), 2,2-bis(4-hydroxyphenyl) butane, 2,2-bis(4-hydroxyphenyl) octane, 1,1-bis(4-hydroxyphenyl) propane, 1,1-bis(4-hydroxyphenyl) n-butane, 2,2-bis(4-hydroxy-1-methylphenyl) propane, and 1,1-bis(4-hydroxy-t-butylphenyl) propane, and combinations comprising at least one of the foregoing compounds.

In one embodiment, the functional aliphatic compound of formula (16) may be an alpha, omega dicarboxylic acid, such that the X groups in formula (16) are each —COOH, or it may be an alpha, omega diester, such that the X groups in formula (16) are each COOR² wherein each R² is independently a C₁-C₁₈ monovalent hydrocarbon, and R of formula (16) is an aliphatic, divalent radical having from about 4 to about 18 carbons. The alpha, omega dicarboxylic acid or ester may therefore be represented by formula (17):

wherein R is an aliphatic, divalent radical having from about 4 to about 18 carbons, and each W is a hydrogen or R², as previously defined above. For example, R may be represented by (CH₂)_n, where n is from about 4 to about 18. Examples of dicarboxylic acids or esters suitable for use include, but are not limited to, adipic acid, heptanedioic (pimelic) acid, suberic acid, nonanedioic (azelaic) acid, decanedioic (sebacic) acid, and dodecanedioic acid. The repeating units of formula (1) are present an amount of from about 2 to about 30 mole percent. Illustrative examples of compounds suitable for use as the carbonate units of formula (1) include 1,1-bis(4-hydroxyphenyl) methane, 1,1-bis(4-hydroxyphenyl) ethane, 2,2-bis(4-hydroxyphenyl) propane (hereinafter “bisphenol A” or “BPA”), 2,2-bis(4-hydroxyphenyl) butane, 2,2-bis(4-hydroxyphenyl) octane, 1,1-bis(4-hydroxyphenyl) propane, 1,1-bis(4-hydroxyphenyl) n-butane, 2,2-bis(4-hydroxy-1-methylphenyl) propane, and 1,1-bis(4-hydroxy-t-butylphenyl) propane, and combinations comprising at least one of the foregoing compounds.

In addition to the impact modifier, the composition further comprises an ungrafted rigid copolymer. The rigid copolymer is additional to any rigid copolymer present in the impact modifier. It may be the same as any of the rigid copolymers described above, without the elastomer modification. The rigid copolymers generally have a Tg greater than about 15° C., specifically greater than about 20° C., and include, for example, polymers derived from monovinylaromatic monomers containing condensed aromatic ring structures, such as vinyl naphthalene, vinyl anthracene and the like, or monomers of formula (9) as broadly described above, for example styrene and alpha-methyl styrene; monovinylic monomers such as itaconic acid, acrylamide, N-substituted acrylamide or methacrylamide, maleic anhydride, maleimide, N-alkyl, aryl or haloaryl substituted maleimide, glycidyl (meth)acrylates, and monomers of the general formula (10) as broadly described above, for example acrylonitrile, methyl acrylate and methyl methacrylate; and copolymers of the foregoing, for example styrene-acrylonitrile (SAN), styrene-alpha-methyl styrene-acrylonitrile, methyl methacrylate-acrylonitrile-styrene, and methyl methacrylate-styrene.

The rigid copolymer may comprise about 1 to about 99 wt. %, specifically about 20 to about 95 wt. %, more specifically about 40 to about 90 wt. % of vinylaromatic monomer, together with 1 to about 99 wt. %, specifically about 5 to about 80 wt. %, more specifically about 10 to about 60 wt. % of copolymerizable monovinylic monomers. In one embodiment the rigid copolymer is SAN, which may comprise about 50 to about 99 wt. % styrene, with the balance acrylonitrile, specifically about 60 to about 90 wt. % styrene, and more specifically about 65 to about 85 wt. % styrene, with the remainder acrylonitrile.

The rigid copolymer may be manufactured by bulk, suspension, or emulsion polymerization, and is substantially free of impurities, residual acids, residual bases or residual metals that may catalyze the hydrolysis of polycarbonate. In one embodiment, the rigid copolymer is manufactured by bulk polymerization using a boiling reactor. The rigid copolymer may have a weight average molecular weight of about 50,000 to about 300,000 as measured by GPC using polystyrene standards. In one embodiment, the weight average molecular weight of the rigid copolymer is about 50,000 to about 200,000.

The relative amount of each component of the thermoplastic composition will depend on the particular type of polycarbonate(s) used, the presence of any other resins, and the particular impact modifier(s), including any optional rigid graft copolymer, as well as the desired properties of the composition. Particular amounts may be readily selected by one of ordinary skill in the art using the guidance provided herein.

In one embodiment, the thermoplastic composition comprises about 1 to about 95 wt. % polycarbonate component, about 5 to about 98 wt. % bulk polymerized ABS, and about 1 to about 95 wt. % additional elastomer-modified impact modifier. In another embodiment, the thermoplastic composition comprises about 10 to about 90 wt. % polycarbonate component, about 5 to about 75 wt. % bulk polymerized ABS, and about 1 to about 30 wt. % other elastomer-modified impact modifier. In another embodiment, the thermoplastic composition comprises about 20 to about 84 wt. % polycarbonate component, about 5 to about 50 wt. % bulk polymerized ABS, and about 4 to about 20 wt. % additional elastomer-modified impact modifier. In another embodiment, the thermoplastic composition comprises about 64 to about 74 wt. % polycarbonate component, about 5 to about 35 wt. % bulk polymerized ABS, and about 2 to about 10 wt. % additional elastomer-modified impact modifier. In another embodiment, the thermoplastic composition comprises about 68 to about 72 wt. % polycarbonate component, about 17 to about 23 wt. % bulk polymerized ABS, and about 4 to about 8 wt. % additional elastomer-modified impact modifier. The foregoing compositions may further comprise 0 about 50 wt. %, specifically 0 to about 35 wt. %, more specifically about 1 to about 20 wt. %, even more specifically about 3 to about 8 wt. %, most specifically about 6 wt. % of a rigid copolymer. All of the foregoing amounts are based on the combined weight of the polycarbonate composition and the impact modifier composition.

As a specific example of the foregoing embodiments, there is provided a thermoplastic composition that comprises about 65 to about 75 wt. % of a polycarbonate component; about 16 to about 30 wt. % of a bulk polymerized ABS impact modifier; about 1 to about 10 wt. % of MBS; and 0 to about 6 wt. % of a rigid copolymer, for example SAN. Use of the foregoing amounts may provide compositions having enhanced hydrolytic stability together with good thermal stability and impact resistance, particularly at low temperatures.

In addition to the aliphatic/aromatic co-polycarbonate component; an impact modifier; and a rigid copolymer, such as an aromatic vinyl copolymer, and optionally a polycarbonate and/or a polycarbonate-polysiloxane copolymer, the thermoplastic composition may include various additives such as fillers, reinforcing agents, stabilizers, and the like, with the proviso that the additives do not adversely affect the desired properties of the thermoplastic compositions.

The thermoplastic composition may further comprise a low gloss additive. An example of a suitable low gloss additive comprises the reaction product of a polyepoxide and a polymer comprising an ethylenically unsaturated nitrile, and can further comprise a polycarbonate. The components are reactively combined at elevated temperature to form the low gloss additive. Suitable low gloss additives and methods of preparing them are disclosed in U.S. Pat. No. 5,530,062 to Bradtke, which is incorporated herein by reference.

Polyepoxides which are suitable for use in preparing low gloss additives include simple aliphatic diepoxides such as dodecatriene dioxide, dipentene dioxide and 1,2,7,8-diepoxyoctane; bis-glycidyl ethers/esters such as the bisglycidyl ether of bisphenol A and its condensation products; alicyclic diepoxides such as 3,4-epoxycyclohexyl 3,4-epoxycyclohexanecarboxylate and bis(3,4-epoxycyclohexylmethyl) adipate; mixed aliphatic/alicyclic diepoxides such as vinylcyclobutene dioxide, vinylcyclopentadiene dioxide and butenylcyclopentene dioxide; glycidyl ethers of novolak resins; epoxidized heterocycles such as triglycidyl isocyanurate; and epoxidized oils such as epoxidized tall oil, linseed oil and soybean oil; combinations comprising one or more of the foregoing; and the like. Specifically suitable polyepoxides are alicyclic polyepoxides such as 3,4-epoxycyclohexyl 3,4-epoxycyclohexylcarboxylate, available under the trade name ERL-4221 from Union Carbide.

Mixtures of additives may be used. Such additives may be mixed at a suitable time during the mixing of the components for forming the composition. Suitable fillers or reinforcing agents that may be used include, for example, silicates and silica powders such as aluminum silicate (mullite), synthetic calcium silicate, zirconium silicate, fused silica, crystalline silica graphite, natural silica sand, and the like; boron powders such as boron-nitride powder, boron-silicate powders, and the like; oxides such as TiO₂, aluminum oxide, magnesium oxide, and the like; calcium sulfate (as its anhydride, dihydrate or trihydrate); calcium carbonates such as chalk, limestone, marble, synthetic precipitated calcium carbonates, and the like; talc, including fibrous, modular, needle shaped, lamellar talc, and the like; wollastonite; surface-treated wollastonite; glass spheres such as hollow and solid glass spheres, silicate spheres, cenospheres, aluminosilicate (armospheres), and the like; kaolin, including hard kaolin, soft kaolin, calcined kaolin, kaolin comprising various coatings known in the art to facilitate compatibility with the polymeric matrix resin, and the like; single crystal fibers or “whiskers” such as silicon carbide, alumina, boron carbide, iron, nickel, copper, and the like; fibers (including continuous and chopped fibers) such as asbestos, carbon fibers, glass fibers, such as E, A, C, ECR, R, S, D, or NE glasses, and the like; sulfides such as molybdenum sulfide, zinc sulfide and the like; barium species such as barium titanate, barium ferrite, barium sulfate, heavy spar, and the like; metals and metal oxides such as particulate or fibrous aluminum, bronze, zinc, copper and nickel and the like; flaked fillers such as glass flakes, flaked silicon carbide, aluminum diboride, aluminum flakes, steel flakes and the like; fibrous fillers, for example short inorganic fibers such as those derived from blends comprising at least one of aluminum silicates, aluminum oxides, magnesium oxides, and calcium sulfate hemihydrate and the like; natural fillers and reinforcements, such as wood flour obtained by pulverizing wood, fibrous products such as cellulose, cotton, sisal, jute, starch, cork flour, lignin, ground nut shells, corn, rice grain husks and the like; organic fillers such as polytetrafluoroethylene (Teflon™) and the like; reinforcing organic fibrous fillers formed from organic polymers capable of forming fibers such as poly(ether ketone), polyimide, polybenzoxazole, poly(phenylene sulfide), polyesters, polyethylene, aromatic polyamides, aromatic polyimides, polyetherimides, polytetrafluoroethylene, acrylic resins, poly(vinyl alcohol) and the like; as well as additional fillers and reinforcing agents such as mica, clay, feldspar, flue dust, fillite, quartz, quartzite, perlite, tripoli, diatomaceous earth, carbon black, and the like, and combinations comprising at least one of the foregoing fillers and reinforcing agents. The fillers/reinforcing agents may be coated to prevent reactions with the matrix or may be chemically passivated to neutralize catalytic degradation site that might promote hydrolytic or thermal degradation.

The fillers and reinforcing agents may be coated with a layer of metallic material to facilitate conductivity, or surface treated with silanes to improve adhesion and dispersion with the polymeric matrix resin. In addition, the reinforcing fillers may be provided in the form of monofilament or multifilament fibers and may be used either alone or in combination with other types of fiber, through, for example, co-weaving or core/sheath, side-by-side, orange-type or matrix and fibril constructions, or by other methods known to one skilled in the art of fiber manufacture. Suitable cowoven structures include, for example, glass fiber-carbon fiber, carbon fiber-aromatic polyimide (aramid) fiber, and aromatic polyimide fiberglass fiber and the like. Fibrous fillers may be supplied in the form of, for example, rovings, woven fibrous reinforcements, such as 0-90 degree fabrics and the like; non-woven fibrous reinforcements such as continuous strand mat, chopped strand mat, tissues, papers and felts and the like; or three-dimensional reinforcements such as braids. Fillers are generally used in amounts of about 0 to about 100 parts by weight, based on 100 parts by weight of the aliphatic/aromatic co-polycarbonate component, the impact modifier, and the rigid copolymer, and any optional polycarbonate and/or polycarbonate-polysiloxane copolymer.

Suitable antioxidant additives include, for example, alkylated monophenols or polyphenols; alkylated reaction products of polyphenols with dienes, such as tetrakis[methylene(3,5-di-tert-butyl-4-hydroxyhydrocinnamate)] methane, and the like; butylated reaction products of para-cresol or dicyclopentadiene; alkylated hydroquinones; hydroxylated thiodiphenyl ethers; alkylidene-bisphenols; benzyl species; esters of beta-(3,5-di-tert-butyl-4-hydroxyphenyl)-propionic acid with monohydric or polyhydric alcohols; esters of beta-(5-tert-butyl-4-hydroxy-3-methylphenyl)-propionic acid with monohydric or polyhydric alcohols; and the like; and combinations comprising at least one of the foregoing antioxidants. Antioxidants are generally used in amounts of about 0.01 to about 1, specifically about 0.1 to about 0.5 parts by weight, based on 100 parts by weight of parts by weight of the aliphatic/aromatic co-polycarbonate component, the impact modifier, and the rigid copolymer, and any optional polycarbonate and/or polycarbonate-polysiloxane copolymer.

Suitable heat and color stabilizer additives include, for example, organophosphites such as tris(2,4-di-tert-butyl phenyl) phosphite. Heat and color stabilizers are generally used in amounts of about 0.01 to about 5, specifically about 0.05 to about 0.3 parts by weight, based on 100 parts by weight of parts by weight of the aliphatic/aromatic co-polycarbonate component, the impact modifier, and the rigid copolymer, and any optional polycarbonate and/or polycarbonate-polysiloxane copolymer.

Suitable secondary heat stabilizer additives include, for example thioethers and thioesters such as pentaerythritol tetrakis (3-(dodecylthio)propionate), pentaerythritol tetrakis[3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate], dilauryl thiodipropionate, distearyl thiodipropionate, dimyristyl thiodipropionate, ditridecyl thiodipropionate, pentaerythritol octylthiopropionate, dioctadecyl disulphide, and the like, and combinations comprising at least one of the foregoing heat stabilizers. Secondary stabilizers are generally used in amount of about 0.01 to about 5, specifically about 0.03 to about 0.3 parts by weight, based upon 100 parts by weight of parts by weight of the aliphatic/aromatic co-polycarbonate component, the impact modifier, and the rigid copolymer, and any optional polycarbonate and/or polycarbonate-polysiloxane copolymer.

Light stabilizers, including ultraviolet light (UV) absorbing additives, may also be used. Suitable stabilizing additives of this type include, for example, benzotriazoles and hydroxybenzotriazoles such as 2-(2-hydroxy-5-methylphenyl)benzotriazole, 2-(2-hydroxy-5-tert-octylphenyl)-benzotriazole, 2-(2H-benzotriazol-2-yl)-4-(1,1,3,3-tetramethylbutyl)-phenol (CYASORB™ 5411 from Cytec), and TINUVIN™ 234 from Ciba Specialty Chemicals; hydroxybenzotriazines; hydroxyphenyl-triazine or -pyrimidine UV absorbers such as TINUVIN™ 1577 (Ciba), and 2-[4,6-bis(2,4-dimethylphenyl)-1,3,5-triazin-2-yl]-5-(octyloxy)-phenol (CYASORB™ 1164 from Cytec); non-basic hindered amine light stabilizers (hereinafter “HALS”), including substituted piperidine moieties and oligomers thereof, for example 4-piperidinol derivatives such as TINUVIN™ 622 (Ciba), GR-3034, TINUVIN™ 123, and TINUVIN™ 440; benzoxazinones, such as 2,2′-(1,4-phenylene)bis(4H-3,1-benzoxazin-4-one) (CYASORB™ UV-3638); hydroxybenzophenones such as 2-hydroxy-4-n-octyloxybenzophenone (CYASORB™ 531); oxanilides; cyanoacrylates such as 1,3-bis[(2-cyano-3,3-diphenylacryloyl)oxy]-2,2-bis[[(2-cyano-3,3-diphenylacryloyl)oxy]methyl]propane (UVINUL™ 3030) and 1,3-bis[(2-cyano-3,3-diphenylacryloyl)oxy]-2,2-bis[[(2-cyano-3,3-diphenylacryloyl)oxy]methyl]propane; and nano-size inorganic materials such as titanium oxide, cerium oxide, and zinc oxide, all with particle size less than about 100 nanometers; and the like, and combinations comprising at least one of the foregoing stabilizers. Light stabilizers may be used in amounts of about 0.01 to about 10, specifically about 0.1 to about 1 parts by weight, based on 100 parts by weight of parts by weight of the polycarbonate component and the impact modifier composition. UV absorbers are generally used in amounts of about 0.1 to about 5 parts by weight, based on 100 parts by weight of the aliphatic/aromatic co-polycarbonate component, the impact modifier, and the rigid copolymer, and any optional polycarbonate and/or polycarbonate-polysiloxane copolymer.

Plasticizers, lubricants, and/or mold release agents additives may also be used. There is considerable overlap among these types of materials, which include, for example, phthalic acid esters such as dioctyl-4,5-epoxy-hexahydrophthalate; tris-(octoxycarbonylethyl)isocyanurate; tristearin; di- or polyfunctional aromatic phosphates such as resorcinol tetraphenyl diphosphate (RDP), the bis(diphenyl) phosphate of hydroquinone and the bis(diphenyl) phosphate of bisphenol-A; poly-alpha-olefins; epoxidized soybean oil; silicones, including silicone oils; esters, for example, fatty acid esters such as alkyl stearyl esters, e.g., methyl stearate; stearyl stearate, pentaerythritol tetrastearate, and the like; mixtures of methyl stearate and hydrophilic and hydrophobic nonionic surfactants comprising polyethylene glycol polymers, polypropylene glycol polymers, and copolymers thereof, e.g., methyl stearate and polyethylene-polypropylene glycol copolymers in a suitable solvent; waxes such as beeswax, montan wax, paraffin wax and the like; and poly alpha olefins such as Ethylflo 164, 166, 168, and 170. Such materials are generally used in amounts of about 0.1 to about 20 parts by weight, specifically about 1 to about 10 parts by weight, based on 100 parts by weight of the aliphatic/aromatic co-polycarbonate component, the impact modifier, and the rigid copolymer, and any optional polycarbonate and/or polycarbonate-polysiloxane copolymer.

Colorants such as pigment and/or dye additives may also be present. Suitable pigments include for example, inorganic pigments such as metal oxides and mixed metal oxides such as zinc oxide, titanium dioxides, iron oxides and the like; sulfides such as zinc sulfides, and the like; aluminates; sodium sulfo-silicates sulfates, chromates, and the like; carbon blacks; zinc ferrites; ultramarine blue; Pigment Brown 24; Pigment Red 101; Pigment Yellow 119; organic pigments such as azos, di-azos, quinacridones, perylenes, naphthalene tetracarboxylic acids, flavanthrones, isoindolinones, tetrachloroisoindolinones, anthraquinones, anthanthrones, dioxazines, phthalocyanines, and azo lakes; Pigment Blue 60, Pigment Red 122, Pigment Red 149, Pigment Red 177, Pigment Red 179, Pigment Red 202, Pigment Violet 29, Pigment Blue 15, Pigment Green 7, Pigment Yellow 147 and Pigment Yellow 150, and combinations comprising at least one of the foregoing pigments. Pigments may be coated to prevent reactions with the matrix or may be chemically passivated to neutralize catalytic degradation site that might promote hydrolytic or thermal degradation. Pigments are generally used in amounts of about 0.01 to about 10 parts by weight, based on 100 parts by weight of parts by weight of the aliphatic/aromatic co-polycarbonate component, the impact modifier, and the rigid copolymer, and any optional polycarbonate and/or polycarbonate-polysiloxane copolymer.

Suitable dyes are generally organic materials and include, for example, coumarin dyes such as coumarin 460 (blue), coumarin 6 (green), nile red and the like; lanthanide complexes; hydrocarbon and substituted hydrocarbon dyes; polycyclic aromatic hydrocarbon dyes; scintillation dyes such as oxazole or oxadiazole dyes; aryl- or heteroaryl-substituted poly (C_2-8) olefin dyes; carbocyanine dyes; indanthrone dyes; phthalocyanine dyes; oxazine dyes; carbostyryl dyes; napthalenetetracarboxylic acid dyes; porphyrin dyes; bis(styryl)biphenyl dyes; acridine dyes; anthraquinone dyes; cyanine dyes; methine dyes; arylmethane dyes; azo dyes; indigoid dyes, thioindigoid dyes, diazonium dyes; nitro dyes; quinone imine dyes; aminoketone dyes; tetrazolium dyes; thiazole dyes; perylene dyes, perinone dyes; bis-benzoxazolylthiophene (BBOT); triarylmethane dyes; xanthene dyes; thioxanthene dyes; naphthalimide dyes; lactone dyes; fluorophores such as anti-stokes shift dyes which absorb in the near infrared wavelength and emit in the visible wavelength, and the like; luminescent dyes such as 5-amino-9-diethyliminobenzo(a)phenoxazonium perchlorate; 7-amino-4-methylcarbostyryl; 7-amino-4-methylcoumarin; 7-amino-4-trifluoromethylcoumarin; 3-(2′-benzimidazolyl)-7-N,N-diethylaminocoumarin; 3-(2′-benzothiazolyl)-7-diethylaminocoumarin; 2-(4-biphenyl yl)-5-(4-t-butylphenyl)-1,3,4-oxadiazole; 2-(4-biphenylyl)-5-phenyl-1,3,4-oxadiazole; 2-(4-biphenyl)-6-phenylbenzoxazole-1,3; 2,5-bis-(4-biphenylyl)-1,3,4-oxadiazole; 2,5-bis-(4-biphenylyl)-oxazole; 4,4′-bis-(2-butyloctyloxy)-p-quaterphenyl; p-bis(o-methylstyryl)-benzene; 5,9-diaminobenzo(a)phenoxazonium perchlorate; 4-dicyanomethylene-2-methyl-6-(p-dimethylaminostyryl)-4H-pyran; 1,1′-diethyl-2,2′-carbocyanine iodide; 1,1′-diethyl-4,4′-carbocyanine iodide; 3,3′-diethyl-4,4′,5,5′-dibenzothiatricarbocyanine iodide; 1,1′-diethyl-4,4′-dicarbocyanine iodide; 1,1′-diethyl-2,2′-dicarbocyanine iodide; 3,3′-diethyl-9,11-neopentylenethiatricarbocyanine iodide; 1,3′-diethyl-4,2′-quinolyloxacarbocyanine iodide; 1,3′-diethyl-4,2′-quinolylthiacarbocyanine iodide; 3-diethylamino-7-diethyliminophenoxazonium perchlorate; 7-diethylamino-4-methylcoumarin; 7-diethylamino-4-trifluoromethylcoumarin; 7-diethylaminocoumarin; 3,3′-diethyloxadicarbocyanine iodide; 3,3′-diethylthiacarbocyanine iodide; 3,3′-diethylthiadicarbocyanine iodide; 3,3′-diethylthiatricarbocyanine iodide; 4,6-dimethyl-7-ethylaminocoumarin; 2,2′-dimethyl-p-quaterphenyl; 2,2-dimethyl-p-terphenyl; 7-dimethylamino-1-methyl-4-methoxy-8-azaquinolone-2; 7-dimethylamino-4-methylquinolone-2; 7-dimethylamino-4-trifluoromethylcoumarin; 2-(4-(4-dimethylaminophenyl)-1,3-butadienyl)-3-ethylbenzothiazolium perchlorate; 2-(6-(p-dimethylaminophenyl)-2,4-neopentylene-1,3,5-hexatrienyl)-3-methylbenzothiazolium perchlorate; 2-(4-(p-dimethylaminophenyl)-1,3-butadienyl)-1,3,3-trimethyl-3H-indolium perchlorate; 3,3′-dimethyloxatricarbocyanine iodide; 2,5-diphenylfuran; 2,5-diphenyloxazole; 4,4′-diphenylstilbene; 1-ethyl-4-(4-(p-dimethylaminophenyl)-1,3-butadienyl)-pyridinium perchlorate; 1-ethyl-2-(4-(p-dimethylaminophenyl)-1,3-butadienyl)-pyridinium perchlorate; 1-ethyl-4-(4-(p-dimethylaminophenyl)-1,3-butadienyl)-quinolium perchlorate; 3-ethylamino-7-ethylimino-2,8-dimethylphenoxazin-5-ium perchlorate; 9-ethylamino-5-ethylamino-10-methyl-5H-benzo(a) phenoxazonium perchlorate; 7-ethylamino-6-methyl-4-trifluoromethylcoumarin; 7-ethylamino-4-trifluoromethylcoumarin; 1,1′,3,3,3′,3′-hexamethyl-4,4′,5,5′-dibenzo-2,2′-indotricarboccyanine iodide; 1,1′,3,3,3′,3′-hexamethylindodicarbocyanine iodide; 1,1′,3,3,3′,3′-hexamethylindotricarbocyanine iodide; 2-methyl-5-t-butyl-p-quaterphenyl; N-methyl-4-trifluoromethylpiperidino-<3,2-g>coumarin; 3-(2′-N-methylbenzimidazolyl)-7-N,N-diethylaminocoumarin; 2-(1-naphthyl)-5-phenyloxazole; 2,2′-p-phenylen-bis(5-phenyloxazole); 3,5,3″″,5″″-tetra-t-butyl-p-sexiphenyl; 3,5,3″″,5″″-tetra-t-butyl-p-quinquephenyl; 2,3,5,6-1H,4H-tetrahydro-9-acetylquinolizino-<9,9a,1-gh>coumarin; 2,3,5,6-1H,4H-tetrahydro-9-carboethoxyquinolizino-<9,9a,1-gh>coumarin; 2,3,5,6-1H,4H-tetrahydro-8-methylquinolizino-<9,9a,1-gh>coumarin; 2,3,5,6-1H,4H-tetrahydro-9-(3-pyridyl)-quinolizino-<9,9a,1-gh>coumarin; 2,3,5,6-1H,4H-tetrahydro-8-trifluoromethylquinolizino-<9,9a,1-gh>coumarin; 2,3,5,6-1H,4H-tetrahydroquinolizino-<9,9a,1-gh>coumarin; 3,3′,2″,3′″-tetramethyl-p-quaterphenyl; 2,5,2″″,5′″-tetramethyl-p-quinquephenyl; P-terphenyl; P-quaterphenyl; nile red; rhodamine 700; oxazine 750; rhodamine 800; IR 125; IR 144; IR 140; IR 132; IR 26; IR5; diphenylhexatriene; diphenylbutadiene; tetraphenylbutadiene; naphthalene; anthracene; 9,10-diphenylanthracene; pyrene; chrysene; rubrene; coronene; phenanthrene and the like, and combinations comprising at least one of the foregoing dyes. Dyes are generally used in amounts of about 0.1 parts per million to about 10 parts by weight, based on 100 parts by weight of parts by weight of the aliphatic/aromatic co-polycarbonate component, the impact modifier, and the rigid copolymer, and any optional polycarbonate and/or polycarbonate-polysiloxane copolymer.

Monomeric, oligomeric, or polymeric antistatic additives that may be sprayed onto the article or processed into the thermoplastic composition may be advantageously used. Examples of monomeric antistatic agents include long chain esters such as glycerol monostearate, glycerol distearate, glycerol tristearate, and the like, sorbitan esters, and ethoxylated alcohols, alkyl sulfates, alkylarylsulfates, alkylphosphates, alkylaminesulfates, alkyl sulfonate salts such as sodium stearyl sulfonate, sodium dodecylbenzenesulfonate and the like, fluorinated alkylsulfonate salts, betaines, and the like. Combinations of the foregoing antistatic agents may be used. Exemplary polymeric antistatic agents include certain polyetheresters, each containing polyalkylene glycol moieties such as polyethylene glycol, polypropylene glycol, polytetramethylene glycol, and the like. Such polymeric antistatic agents are commercially available, and include, for example PELESTAT™ 6321 (Sanyo), PEBAX™ MH1657 (Atofina), and IRGASTAT™ P18 and P22 (Ciba-Geigy). Other polymeric materials that may be used as antistatic agents are inherently conducting polymers such as polythiophene (commercially available from Bayer), which retains some of its intrinsic conductivity after melt processing at elevated temperatures. In one embodiment, carbon fibers, carbon nanofibers, carbon nanotubes, carbon black or any combination of the foregoing may be used in a polymeric resin containing chemical antistatic agents to render the composition electrostatically dissipative. Antistatic agents are generally used in amounts of about 0.1 to about 10 parts by weight, specifically about based on 100 parts by weight of the aliphatic/aromatic co-polycarbonate component, the impact modifier, and the rigid copolymer, and any optional polycarbonate and/or polycarbonate-polysiloxane copolymer.

Where a foam is desired, suitable blowing agents include, for example, low boiling halohydrocarbons and those that generate carbon dioxide; blowing agents that are solid at room temperature and when heated to temperatures higher than their decomposition temperature, generate gases such as nitrogen, carbon 25 dioxide ammonia gas, such as azodicarbonamide, metal salts of azodicarbonamide, 4,4′-oxybis(benzenesulfonylhydrazide), sodium bicarbonate, ammonium carbonate, and the like, or combinations comprising at least one of the foregoing blowing agents. Blowing agents are generally used in amounts of about 0.5 to about 20 parts by weight, based on 100 parts by weight of the aliphatic/aromatic co-polycarbonate component, the impact modifier, and the rigid copolymer, and any optional polycarbonate and/or polycarbonate-polysiloxane copolymer.

Suitable flame retardant that may be added are stable, specifically hydrolytically stable. A hydrolytically stable flame retardant does not substantially degrade under conditions of manufacture and/or use to generate species that can catalyze or otherwise contribute to the degradation of the polycarbonate composition. Such flame retardants may be organic compounds that include phosphorus, bromine, and/or chlorine. The polysiloxane-polycarbonate copolymers described above may also be used. Non-brominated and non-chlorinated phosphorus-containing flame retardants may be preferred in certain applications for regulatory reasons, for example certain organic phosphates and/or organic compounds containing phosphorus-nitrogen bonds.

One type of exemplary organic phosphate is an aromatic phosphate of the formula (GO)₃P═O, wherein each G is independently an alkyl, cycloalkyl, aryl, alkaryl, or aralkyl group, provided that at least one G is an aromatic group. Two of the G groups may be joined together to provide a cyclic group, for example, diphenyl pentaerythritol diphosphate, which is described by Axelrod in U.S. Pat. No. 4,154,775. Other suitable aromatic phosphates may be, for example, phenyl bis(dodecyl) phosphate, phenyl bis(neopentyl) phosphate, phenyl bis(3,5,5′-trimethylhexyl) phosphate, ethyl diphenyl phosphate, 2-ethylhexyl di(p-tolyl) phosphate, bis(2-ethylhexyl) p-tolyl phosphate, tritolyl phosphate, bis(2-ethylhexyl) phenyl phosphate, tri(nonylphenyl) phosphate, bis(dodecyl) p-tolyl phosphate, dibutyl phenyl phosphate, 2-chloroethyl diphenyl phosphate, p-tolyl bis(2,5,5′-trimethylhexyl) phosphate, 2-ethylhexyl diphenyl phosphate, and the like. A specific aromatic phosphate is one in which each G is aromatic, for example, triphenyl phosphate, tricresyl phosphate, isopropylated triphenyl phosphate, and the like.

Di- or polyfunctional aromatic phosphorus-containing compounds are also useful, for example, compounds of the formulas below: wherein each G¹ is independently a hydrocarbon having 1 to about 30 carbon atoms; each G² is independently a hydrocarbon or hydrocarbonoxy having 1 to about 30 carbon atoms; each X is independently a bromine or chlorine; m is 0 to 4, and n is 1 to about 30. Examples of suitable di- or polyfunctional aromatic phosphorus-containing compounds include resorcinol tetraphenyl diphosphate (RDP), the bis(diphenyl) phosphate of hydroquinone and the bis(diphenyl) phosphate of bisphenol-A, respectively, their oligomeric and polymeric counterparts, and the like.

Exemplary suitable flame retardant compounds containing phosphorus-nitrogen bonds include phosphonitrilic chloride and tris(aziridinyl) phosphine oxide. When present, phosphorus-containing flame retardants are generally present in amounts of about 1 to about 20 parts by weight, based on 100 parts by weight of the aliphatic/aromatic co-polycarbonate component, the impact modifier, and the rigid copolymer, and any optional polycarbonate and/or polycarbonate-polysiloxane copolymer.

Halogenated materials may also be used as flame retardants, for example halogenated compounds and resins of the formula (18): wherein R is an alkylene, alkylidene or cycloaliphatic linkage, such as methylene, propylene, isopropylidene, cyclohexylene, cyclopentylidene, and others; an oxygen ether, carbonyl, amine, or a sulfur containing linkage, such as, sulfide, sulfoxide, sulfone, and others; or two or more alkylene or alkylidene linkages connected by such groups as aromatic, amino, ether, carbonyl, sulfide, sulfoxide, sulfone, and other groups; Ar and Ar′ are each independently a mono- or polycarbocyclic aromatic group such as phenylene, biphenylene, terphenylene, naphthylene, and others, wherein hydroxyl and Y substituents on Ar and Ar′ can be varied in the ortho, meta or para positions on the aromatic rings and the groups can be in any possible geometric relationship with respect to one another; each Y is independently an organic, inorganic or organometallic radical, for example (1) a halogen such as chlorine, bromine, iodine, or fluorine, (2) an ether group of the general formula —OE, wherein E is a monovalent hydrocarbon radical similar to X, (3) monovalent hydrocarbon groups of the type represented by R or (4) other substituents, e.g., nitro, cyano, and the like, said substituents being essentially inert provided there be at least one and preferably two halogen atoms per aryl nucleus; each X is independently a monovalent C_1-18 hydrocarbon group such as methyl, propyl, isopropyl, decyl, phenyl, naphthyl, biphenyl, xylyl, tolyl, benzyl, ethylphenyl, cyclopentyl, cyclohexyl, and the like, each optionally containing inert substituents; each d is independently 1 to a maximum equivalent to the number of replaceable hydrogens substituted on the aromatic rings comprising Ar or Ar′; each e is independently 0 to a maximum equivalent to the number of replaceable hydrogens on R; and each a, b, and c is independently a whole number, including 0, with the proviso that when b is 0, either a or c, but not both, may be 0, and when b is not 0, neither a nor c may be 0.

Included within the scope of the above formula are bisphenols of which the following are representative: bis(2,6-dibromophenyl)methane; 1,1-bis-(4-iodophenyl)ethane; 2,6-bis(4,6-dichloronaphthyl)propane; 2,2-bis(2,6-dichlorophenyl)pentane; bis(4-hydroxy-2,6-dichloro-3-methoxyphenyl)methane; and 2,2-bis(3-bromo-4-hydroxyphenyl)propane. Also included within the above structural formula are 1,3-dichlorobenzene, 1,4-dibrombenzene, and biphenyls such as 2,2′-dichlorobiphenyl, polybrominated 1,4-diphenoxybenzene, 2,4′-dibromobiphenyl, and 2,4′-dichlorobiphenyl as well as decabromo diphenyl oxide, and the like. Also useful are oligomeric and polymeric halogenated aromatic compounds, such as a copolycarbonate of bisphenol A and tetrabromobisphenol A and a carbonate precursor, e.g., phosgene. Metal synergists, e.g., antimony oxide, may also be used with the flame retardant. When present, halogen containing flame retardants are generally used in amounts of about 1 to about 50 parts by weight, based on 100 parts by weight of the polycarbonate component and the impact modifier composition.

Another useful type of flame retardant is a polysiloxane-polycarbonate copolymer having polydiorganosiloxane blocks comprise repeating structural units of formula (13), previously described. D in formula (13) is selected so as to provide an effective level of flame retardance to the polycarbonate composition. The value of D will therefore vary depending on the relative amount of each component in the polycarbonate composition, including the amount of polycarbonate, impact modifier, polysiloxane-polycarbonate copolymer, and other flame retardants. Suitable values for D may be determined by one of ordinary skill in the art without undue experimentation using the guidelines taught herein. Generally, D has an average value of 10 to about 250, specifically about 10 to about 60.

In one embodiment, M is independently bromo or chloro, a C₁-C₃ alkyl group such as methyl, ethyl, or propyl, a C₁-C₃ alkoxy group such as methoxy, ethoxy, or propoxy, or a C₆-C₇ aryl group such as phenyl, chlorophenyl, or tolyl; R² is a dimethylene, trimethylene or tetramethylene group; and R is a C_1-8 alkyl, haloalkyl such as trifluoropropyl, cyanoalkyl, or aryl such as phenyl, chlorophenyl or tolyl. In another embodiment, R is methyl, or a mixture of methyl and trifluoropropyl, or a mixture of methyl and phenyl. In still another embodiment, M is methoxy, n is one, R² is a divalent C₁-C₃ aliphatic group, and R is methyl.

Inorganic flame retardants may also be used, for example salts of C_2-16 alkyl sulfonates such as potassium perfluorobutane sulfonate (Rimar salt), potassium perfluorooctane sulfonate, tetraethylammonium perfluorohexane sulfonate, and potassium diphenylsulfone sulfonate; salts such as CaCO₃, BaCO₃, and BaCO₃; salts of fluoro-anion complex such as Li₃AlF₆, BaSiF₆, KBF₄, K₃AlF₆, KAlF₄, K₂SiF₆, and Na₃AlF₆; and the like. When present, inorganic flame retardant salts are generally present in amounts of about 0.01 to about 25 parts by weight, more specifically about 0.1 to about 10 parts by weight, based on 100 parts by weight of the aliphatic/aromatic co-polycarbonate component, the impact modifier, and the rigid copolymer, and any optional polycarbonate and/or polycarbonate-polysiloxane copolymer.

Anti-drip agents may also be used, for example a fibril forming or non-fibril forming fluoropolymer such as polytetrafluoroethylene (PTFE). The anti-drip agent may be encapsulated by a rigid copolymer as described above, for example SAN. PTFE encapsulated in SAN is known as TSAN. Encapsulated fluoropolymers may be made by polymerizing the encapsulating polymer in the presence of the fluoropolymer, for example an aqueous dispersion. TSAN may provide significant advantages over PTFE, in that TSAN may be more readily dispersed in the composition. A suitable TSAN may comprise, for example, about 50 wt. % PTFE and about 50 wt. % SAN, based on the total weight of the encapsulated fluoropolymer. The SAN may comprise, for example, about 75 wt. % styrene and about 25 wt. % acrylonitrile based on the total weight of the copolymer. Alternatively, the fluoropolymer may be pre-blended in some manner with a second polymer, such as for, example, an aromatic polycarbonate resin or SAN to form an agglomerated material for use as an anti-drip agent. Either method may be used to produce an encapsulated fluoropolymer. Antidrip agents are generally used in amounts of about 0.1 to about 10 parts by weight, based on 100 parts by weight of the aliphatic/aromatic co-polycarbonate component, the impact modifier, and the rigid copolymer, and any optional polycarbonate and/or polycarbonate-polysiloxane copolymer.

The thermoplastic compositions may be manufactured by methods generally available in the art, for example, in one embodiment, in one manner of proceeding, powdered polycarbonate, other resin if used, impact modifier composition, co-polycarbonate, rigid copolymer, and/or other optional components are first blended, optionally with any fillers in a Henschel™ type high speed mixer. Other low shear processes including but not limited to hand mixing may also accomplish this blending. The blend is then fed into the throat of a twin-screw extruder via a hopper. Alternatively, one or more of the components may be incorporated into the composition by feeding directly into the extruder at the throat and/or downstream through a sidestuffer. Other processing methods, such as a single screw extruder, Buss™ kneader, Banbury™ mixer, and the like, may be used for processing, as known to a skilled artisan. Such additives may also be compounded into a masterbatch with a desired polymeric resin and fed into the extruder. The additives may be added to either the polycarbonate base materials or the impact modifier base material to make a concentrate, before this is added to the final product. The extruder is generally operated at a temperature higher than that necessary to cause the composition to flow, typically 500° F. (260° C.) to 650° F. (343° C.). The extrudate is immediately quenched in a water batch and pelletized. The pellets, so prepared, when cutting the extrudate may be one-fourth inch long or less as desired. Such pellets may be used for subsequent molding, shaping, or forming.

Shaped, formed, or molded articles comprising the thermoplastic compositions are also provided. The thermoplastic compositions may be molded into useful shaped articles by a variety of means such as injection molding, extrusion, rotational molding, blow molding and thermoforming to form articles such as, for example, computer and business machine housings such as housings for monitors, handheld electronic device housings such as housings for cell phones, electrical connectors, and components of lighting fixtures, ornaments, home appliances, roofs, greenhouses, sun rooms, swimming pool enclosures, and others.

The compositions find particular utility in automotive applications, for example interior parts such as instrument panels, overhead consoles, interior trim, center consoles, and other interior parts; and exterior parts such as body panels, exterior trim, bumpers, and others.

The compositions described herein may further have excellent physical properties and good processability. For example, the thermoplastic polycarbonate compositions may have a heat deflection temperature (HDT) of about 80 to about 120° C., more specifically about 90 to about 115° C., measured at 1.8 MPa, and about 100 to about 150° C., more specifically about 110 to about 135° C., measured at 0.45 MPa, on a 4 mm thick bar according to ISO 75Ae.

The thermoplastic polycarbonate compositions may further have a low temperature notched Izod Impact of greater than about 15 KJ/m², specifically greater than about 25 KJ/m², determined at −30° C. using a 4 mm thick bar per ISO 180/1A.

The thermoplastic polycarbonate compositions may further have a Charpy Impact of great than about 15 KJ/m² determined at −30° C., more specifically great than about 25 KJ/m², determined at −30° C., determined using a 4 mm thick per ISO 179/1 eA.

The thermoplastic polycarbonate compositions may further have a Vicat B/50 of greater than about 100° C., more specifically greater than about 120° C., determined using a 4 mm thick bar per ISO 306.

The thermoplastic polycarbonate compositions may further have a Instrumented Impact Energy (dart impact) at maximum load of at least about 15, specifically at least about 25 ft-lbs, determined using a 4-inch (10 cm) diameter disk at −30° C., ½-inch (12.7 mm) diameter dart, and an impact velocity of 6.6 meters per second (m/s) per ASTM D3763.

The thermoplastic polycarbonate compositions may further have a 60° Gloss of less than about 30, specifically less than about 10, determined using a Gardner Gloss Meter and 3 millimeter color chips.

The invention is further illustrated by the following non-limiting Examples, which were prepared from the components set forth in Table 1.

TABLE 1
Component	Type	Source
PC-1	High Flow BPA branched polycarbonate resin made	GE Plastics
	by a interfacial process with a molecular weight of
	about 22,000 on an absolute PC molecular weight scale
PC-2	Low Flow BPA branched polycarbonate resin made	GE Plastics
	by a interfacial process with a molecular weight of
	about 30,000 on an absolute PC molecular weight scale
MBS	Nominal 75-82 wt. % butadiene core with a balance	Rohm & Haas
	of styrene-methyl methacrylate shell. (Trade name
	EXL 2691A)
BABS	Bulk Acrylonitrile Butadiene Styrene with nominal	GE Plastics
	16% butadiene and content and nominal 15%
	acrylonitile content, phase inverted with occluded
	SAN in a butadiene phase in SAN matrix
Co-poly 1*	Co-polycarbonate comprising repeating units of	*Prepared by
	butanediol (about 4 to 5 mole percent nominal) and	method described
	repeating units of high flow bisphenol A
	polycarbonate, with a molecular weight of about
	22,000 on an absolute PC molecular weight scale
Co-poly 2*	Co-polycarbonate comprising repeating units of	*Prepared by
	butanediol (about 4 to 5 mole percent nominal) and	method described
	repeating units of low flow bisphenol A
	polycarbonate, with a molecular weight of about
	30,000 on an absolute PC molecular weight scale
Co-poly 3*	Mixed aliphatic/aromatic co-polycarbonate	*Prepared by
	comprising repeating units of dodecanedioic acid	method described
	(about 8 to 9 mole percent) and repeating units of
	bisphenol A polycarbonate, with a molecular weight
	of about 30,000 on an absolute PC molecular
	weight scale
SAN	Styrene acrylonitrile copolymer comprising 15-35	GE Plastics
	wt. % acrylonitrile (nominally 25 wt. %), bulk
	processed, molecular weight of about 77,000
	(Calibrated on Polystyrene standards based GPC
	weight average molecular weight)
PC-Si	Polydimethylsiloxane - bisphenol A polycarbonate	GE Plastics
	copolymer, 20 wt % polydimethylsiloxane content,
	Mw about 30,000
*Co-poly 1 and Co-poly 2 were prepared according to the method for making the co-polycarbonates described above and in copending U.S. application Ser. No. 10/968,773, filed Oct. 19, 2004. Co-poly 3 was prepared according to the method of U.S. Pat. Nos. 5,025,081 and 5,510,448.

In the examples below, the polycarbonates (PC) are based on Bisphenol A, and have a molecular weight of 10,000 to 120,000, more specifically 18,000 to 40,000 (on an absolute molecular weight scale), available from GE Plastics under the trade name LEXAN®. The initial melt flow of the polycarbonates can range from about 2 to about 66 measured at 300° C. using a 1.2 Kg load, per ASTM D1238.

The MBS used in the examples is Rohm & Haas MBS EXL2691A (powder) having 75-82 wt. % butadiene core with a balance styrene-methyl methacrylate shell, but others, such as Rohm & Haas EXL3691A (pelletized) could also be used. The MBS is preferably manufactured in accordance with the process described U.S. Pat. No. 6,545,089, and is substantially free of impurities, residual acids, residual bases or residual metals that may catalyze the hydrolysis of polycarbonate. Control of the manufacture of the MBS to provide a slurry of the MBS having a pH of about 6 to about 7 provides optimal hydrolytic stability. The pH of a slurry of each of the components is measured using 1 g of the component and 10 mL of distilled water having a pH of 7 and containing a drop of isopropyl alcohol as a wetting agent.

The SAN used is a bulk process material having an acrylonitrile content of 25 wt. %, although SAN or other rigid polymers (vinyl aromatic polymers) having different amounts of acrylonitrile and made by either the bulk or suspension process could also be used.

The Bulk Acrylonitrile Butadiene Styrene with nominal 16% butadiene and content and nominal 15% acrylonitile content, phase inverted with occluded SAN in a butadiene phase in SAN matrix from GE Plastics, although ABS or other bulk ABS having different amounts of acrylonitrile and butadiene could also be used.

The co-polycarbonates used were made by a method comprising reacting at least one dihydroxy aromatic compound under interfacial conditions with phosgene and an oligomeric aliphatic chloroformate. The oligomeric aliphatic chloroformate is prepared by a method comprising introducing into a flow reactor at least one oligomeric functional aliphatic compound, phosgene, a solvent, and optionally an organic base to form a unidirectional flowing reaction mixture; and maintaining said unidirectional flowing reaction mixture at a temperature inside the flow reactor in a range between about 0° C. and about 60° C. to produce a product stream comprising an oligomeric aliphatic chloroformate, or by a method comprising reacting a dihydric phenol (such as bisphenol A) with a carbonate precursor and an aliphatic alpha, omega-dicarboxylic acid or ester precursor, wherein the aliphatic alpha, omega-dicarboxylic acid or ester precursor has from 6 to about 20 carbon atoms and is present in the co-polycarbonate in an amount of from about 2 to about 30 mole percent of the dihydric phenol. Details of the methods may be found in copending U.S. application Ser. No. 10/968,773, filed Oct. 19, 2004, and U.S. Pat. Nos. 5,025,081 and 5,510,448, respectively.

The polycarbonate-polysiloxane used is a copolymer of bisphenol-A polycarbonate and polydimethylsiloxane having about 20% siloxane content, although other polycarbonate-polysiloxane copolymers having different siloxane content may also be used.

Samples were prepared by melt extrusion on a Werner & Pfleiderer 30 mm twin screw extruder, using a nominal melt temperature of 525° F. (274° C.), 25 inches (635 mm) of mercury vacuum, and 500 rpm. The extrudate was pelletized and dried at about 120° C. for about 4 hours. To make test specimens, the dried pellets were injection molded on an 85-ton injection molding machine at a nominal temp of 525° C., wherein the barrel temperature of the injection molding machine varied from about 285° C. to about 300° C. Specimens were tested in accordance with ASTM and/or ISO standards as described below.

Tensile properties such as Tensile Strength, Tensile Elongation to Break, Stress at Yield and Break and Chord Modulus were determined using 4 mm thick molded tensile bars tested per ISO 527 at 50 mm/min. It is also possible to measure at 5 mm/min. if desired for the specific application, but the samples measured in these experiments were measured at 50 mm/min. Tensile modulus is always measured at the start of the test with an initial rate of 1 mm/min, after which the test is continued at 50 mm/min. to measure the other tensile properties.

Flexural Modulus and Flexural Strength were determined using a 4 mm-thick bar cut from the tensile bar, pursuant to ISO 178.

Izod Impact Strength was measured according to ISO 180 (‘NII') or ASTM D256 as indicated in the Tables. ISO 180 (‘NII’) is used to compare the impact resistances of plastic materials. ISO Izod Impact was determined using a 4 mm thick test sample cut from the tensile bars described above. It was determined per ISO 180/1A. The ISO designation reflects type of specimen and type of notch: ISO 180/1A means specimen type 1 and notch type A. The ISO results are defined as the impact energy in joules used to break the test specimen, divided by the specimen area at the notch. Results are reported in kJ/m². ASTM D256 is also used, and the ASTM Izod Impact was determined using a molded Izod impact bar 3.2 mm thick, 12.5 mm wide, 3 inches long. The samples were impacted with an impact energy of 5.5 J. Izod impact D/B refers to the ductile transition temperature, which is the temperature at which % ductility equals 50%.

Charpy Notched Impact ISO 179/1 eA is used to compare the impact resistances of plastic materials. Charpy Notched Impact was determined using a 4 mm thick sample cut from the tensile bar previously described. The ISO results are defined as the impact energy in joules used to break the test specimen, divided by the specimen area at the notch. Results are reported in kJ/m². The samples were impacted with an impact energy of 15 J. Charpy D/B refers to the ductile transition temperature, which is the temperature at which % ductility equals 50%.

Vicat Softening Temperature (ISO 306) is a measure of the temperature at which a plastic starts to soften rapidly. A round, flat-ended needle of 1 mm² cross section penetrates the surface of a plastic test specimen under a predefined load, and the temperature is raised at a uniform rate. The Vicat softening temperature, or VST, is the temperature at which the penetration reaches 1 mm. ISO 306 describes two methods: Method A—load of 10 Newtons (N), and Method B—load of 50 N, with two possible rates of temperature rise: 50° C./hour (° C./h) or 120° C./h. This results in ISO values quoted as A/50, A/120, B/50 or B/120. The test assembly is immersed in a heating bath with a starting temperature of 23° C. After 5 minutes (min) the load is applied: 10 N or 50 N. The temperature of the bath at which the indenting tip has penetrated by 1±0.01 mm is reported as the VST of the material at the chosen load and temperature rise. These samples in these experiments were measured under condition B/50.

Heat Deflection Temperature (HDT) is a relative measure of a material's ability to perform for a short time at elevated temperatures while supporting a load. The test measures the effect of temperature on stiffness: a standard test specimen is given a defined surface stress and the temperature is raised at a uniform rate. Heat Deflection Test (HDT) was determined per ISO 75 Af, using a flat, 4 mm thick bar cut from the Tensile bar and subjected to 1.8 MPa and 0.45 MPa.

Instrumented Impact Energy (dart impact) at maximum load was measured using a 4-inch (10 cm) diameter disk at −30° C., ½-inch (12.7 mm) diameter dart, and an impact velocity of 6.6 meters per second (m/s) per ASTM D3763.

Melt Volume Rate (MVR) was determined at 260° C. using a 5-kilogram weight, with a six minute preheat, according to ASTM D1238. In some experiments, Melt Volume Rate was also determined with an eighteen minute preheat according to ASTM D1238. In other experiments, Melt Volume Rate was also measured at 265° C. with a four minute preheat according to ISO 1133.

Melt Viscosity was measured in a capillary rheometer at 640 1/sec at different temperatures as indicated according to ISO 11443. Initial viscosity at 260° C. was measured using a Rheometrics parallel plate rheometer. Viscosity change is the difference between initial value at 6 minutes preheat and after 30 minutes heating under shear, using a Rheometrics parallel plate rheometer. Capillary Rheometry measures apparent viscosity (resistance to flow) over a broad range of shear rates and at varied temperatures, which are comparable to the conditions encountered in molding and extrusion.

Dynatup Energy to maximum load is measured on a plaque 3.2 mm thick, 10 centimeters diameter, with a dart diameter of 12.5 mm at 6.6 m/s according to ASTM D376.

Percent ductility was determined on one-eighth inch (3.2 mm) bars or plaques (for Izod and Dynatup respectively) at room temperature using the impact energy as well as stress whitening of the fracture surface. Generally, significant stress whitening of the fractured surface accompanied by gross deformation at the fractured tip can indicate ductile failure mode; conversely, lack of significant stress whitening of the fractured surface accompanied by gross deformation at the fractured tip can indicate brittle failure mode. Ten bars were tested, and percent ductility is expressed as a percentage of impact bars that exhibited ductile failure mode. Ductility tends to decrease with temperature, and the ductile transition temperature is the temperature at which % ductility equals 50%.

Surface gloss was tested according to ASTM D2457 at 60° using a Gardner Gloss Meter and 3 millimeter color chips and is reported in gloss units (GU) with the gloss level of standard black glass chip as 100 GU. The surface textures are commercially available standard surfaces.

Examples 1 to 21 were produced at various levels of components from Table 1. The formulations used are shown in Table 2 below. All amounts are in weight percent (wt. %). A statistical modeling package was used to generate the plot which is a response surface showing the relationship between composition and melt flow.

TABLE 2
	PC-1	PC-2	MBS	PC-Si	Co-poly 1	Co-poly 2	SAN
Ex. No.	wt. %	wt. %	wt. %	wt. %	wt. %	wt. %	wt. %
1*	0	0	0	10	80	0	10
2	0	80	0	10	0	0	10
3*	13.83	4.62	8.75	8.75	41.48	13.83	8.75
4*	0	0	10	0	0	80	10
5*	19.37	19.37	7.5	7.5	19.37	19.37	7.5
6	0	80	10	10	0	0	0
7*	0	0	10	10	80	0	0
8	0	80	0	10	0	0	10
9	0	70	10	10	0	0	10
10	70	0	10	10	0	0	10
11*	18.75	18.75	8.33	8.33	18.75	18.75	8.34
12*	0	0	9.1	9.1	72.7	0	9.1
13	80	0	10	0	0	0	10
14*	0	0	10	0	80	0	10
15*	45	15	10	10	15	5	0
16*	4.38	13.12	10	10	13.12	39.38	10
17	80	0	0	10	0	0	10
18*	0	0	0	10	80	0	10
19*	0	0	10	10	0	80	0
20	80	0	0	10	0	0	10
21*	15	45	10	0	5	15	10
*Examples of the invention

All of the above samples contained a stabilization package and color concentrate package. The color concentrate package was included in the stabilization package, and the stabilization package was added to the samples. The stabilization package contained 0.4 PETS; 0.5 hindered phenol AO; 0.2 Seenox™ 412 S (thio ester); 0.1 phosphite stabilizer; 0.3 UV stabilizer; 1.59 TiO₂; and 0.93 color concentrate package (all in parts per hundred (phr) polymer). The color concentrate package contained: 36.5 g carbon black; 2.5 g sol red 135; 202 g pigment yellow 183; 188 g pigment green 50; 71 g pigment blue 29; 2400 g PC powder (high flow PC, MW 22,000).

The samples from Table 2 were then tested according to the test methods described above. Results of the tests are shown in Tables 3 to 6 below.

TABLE 3
								Visc.
	MVR	MVR	MVR	Visc. at	Visc. at	Visc. at	Initial	Change
	260° C.,	260° C.,	265° C.,	640 l/sec	640 l/sec	640 l/sec	Visc. at	after 30 min,
	5 kg	5 kg, 18 min	5 kg	260° C.	280° C.	300° C.	260° C.	260° C.
Ex. No.	cm3/10 min	cm3/10 min	cm3/10 min	Pa-s	Pa-s	Pa-s	P	%
1*	27.1	32.4	32.37	393.6	238.8	150	13798	−94
2	19.2	143.1	22.17	571.2	293.5	117.5	14073	−47
3*	16.58	100.7	19.59	640.5	393.1	220.4	16150	−19
4*	46.9	38.9	41.05	384.4	218.7	133.7	11783	−12
5*	13.8	14.43	16.79	503	301	212.2	20751	−12
6	66.2	82.36	78.47	248	131	45.5	3910	−59
7*	33.3	41.44	40	364.9	183.5	80.7	10572	−46
8	5.2	5.03	6.32	1033.6	754.8	536.6	42309	−1.8
9	41.6	28.03	48.87	308.6	203	128.9	6744	−13
10	47.5	67.5	55.79	283.7	148.9	56.9	8179	−52
11*	36.4	45.63	46.62	394.7	198.2	64.4	8613	−44
12*	26.4	21.06	20.57	512.7	305.9	165.1	20215	−30
13	23.1	26.77	27.68	463.5	269.1	121.8	13301	−42
14*	16.5	18.15	23.75	434.2	234.4	110.5	16213	−48
15*	60	38.85	70.99	270.2	125.6	52	6961	−40
16*	30.4	38.6	36.61	382.3	194.4	82.3	12200	−41
17	13.5	10.75	10.27	579.3	397.4	270.7	35706	−13
18*	67.8	47.28	78.44	246.9	130.5	53.1	4168	−58
19*	40.97	25.2	49.32	326.5	200.3	126.7	7158	−13
20	27.1	30.4	26.03	435.3	243.6	122.4	14511	−44
21*	14.4	16.46	15.96	482.4	308.6	212.2	21746	−11
*Examples with * are examples of the invention; those without * are comparative examples

TABLE 4
	Charpy	Charpy	Charpy
	Impact	Impact,	Impact,				ISO	ISO
	at 23° C.,	−30° C.,	−40° C.,	Charpy	Flexural	Flexural	HDT at	HDT at
	5 kg	5 kg	5 kg	D/B	Modulus	Strength	1.8 MPa	0.45 MPa
Ex. No.	kJ/m2	kJ/m2	kJ/m2	° C.	MPa	MPa	° C.	° C.
1*	53.76	46.98	43.26	−64	2056	76.6	105.82	125.05
2	59.11	46.75	44.24	−54	1821	72.48	102.66	115.85
3*	54.69	44.68	41.68	−55	1841.2	74.51	110.8	126.5
4*	53.76	46.7	33.15	−37	2079.6	80.55	107.2	125.95
5*	86.21	23.03	22.45	−35	2191	94.15	113.14	129.05
6	20.55	3.12	31.77	30	2250.75	93.6	96.98	110.2
7*	53.3	44.41	43.18	−34	1858.8	77.45	101.84	115.95
8	59.53	50.15	48.1	−20	1705.6	72.7	118.6	133.4
9	24.8	16.03	8.11	20	2503.25	102.43	109.92	125.55
10	51.04	40.02	33.43	−43	2012.2	76.9	95.64	111.25
11*	50.94	41.16	37.88	−10	1703	71.75	99.68	114.15
12*	64.28	55.62	47.05	−50	2061.6	81.78	107.3	123.55
13	59.06	49.23	48.27	−45	1916.6	79.69	103.94	119.65
14*	59.3	54.79	49.49	−65	1956.4	75.92	101.02	115.55
15*	46.52	21.59	12.93	30	2096	80.99	97.42	109.25
16*	57.29	47.02	36.55	−33	1906.4	79.44	98.72	112.2
17	73.66	66.15	63.43	−65	1941	76.2	109	129.2
18*	18.34	5.12	3.2	40	2397.6	96.83	98.76	110.5
19*	32.53	18.48	8.94	10	2399.4	98.18	111.3	126
20	58.13	50.57	48.91	−55	2009.4	78.74	103.78	119.95
21*	77.56	22.28	23.43	0	2188.2	94.73	112.14	128.75
*Examples of the invention

TABLE 5
	ASTM	ASTM	ASTM		ISO	ISO	ISO	ISO
	Notched	Notched	Notched	ASTM	Notched	Notched	Notched	Notched
	Izod	Izod	Izod	Notched	Izod	Izod	Izod	Izod
	Impact	Impact	Impact	Izod	Impact	Impact	Impact	Impact
	at 23° C.	at −30° C.	at −40° C.	D/B	at 23° C.	at −30° C.	at −40° C.	D/B
Ex. No.	ft.lbs/in	ft.lbs/in	ft.lbs/in	° C.	kJ/m2	kJ/m2	kJ/m2	° C.
1*	53.76	46.98	43.26	−64	2056	76.6	105.82	125.05
2	59.11	46.75	44.24	−54	1821	72.48	102.66	115.85
3*	54.69	44.68	41.68	−55	1841.2	74.51	110.8	126.5
4*	53.76	46.7	33.15	−37	2079.6	80.55	107.2	125.95
5*	86.21	23.03	22.45	−35	2191	94.15	113.14	129.05
6	20.55	3.12	31.77	30	2250.75	93.6	96.98	110.2
7*	53.3	44.41	43.18	−34	1858.8	77.45	101.84	115.95
8	59.53	50.15	48.1	−20	1705.6	72.7	118.6	133.4
9	24.8	16.03	8.11	20	2503.25	102.43	109.92	125.55
10	51.04	40.02	33.43	−43	2012.2	76.9	95.64	111.25
11*	50.94	41.16	37.88	−10	1703	71.75	99.68	114.15
12*	64.28	55.62	47.05	−50	2061.6	81.78	107.3	123.55
13	59.06	49.23	48.27	−45	1916.6	79.69	103.94	119.65
14*	59.3	54.79	49.49	−65	1956.4	75.92	101.02	115.55
15*	46.52	21.59	12.93	30	2096	80.99	97.42	109.25
16*	57.29	47.02	36.55	−33	1906.4	79.44	98.72	112.2
17	73.66	66.15	63.43	−65	1941	76.2	109	129.2
18*	18.34	5.12	3.2	40	2397.6	96.83	98.76	110.5
19*	32.53	18.48	8.94	10	2399.4	98.18	111.3	126
20	58.13	50.57	48.91	−55	2009.4	78.74	103.78	119.95
21*	77.56	22.28	23.43	0	2188.2	94.73	112.14	128.75
*Examples of the invention

TABLE 6
	Dyn.	Dyn.
	Energy to	Energy to
	Max Load	Max Load	Chord	Stress @		Gloss at	Gloss at
	at 23° C.,	at	Modulus	Yield	Vicat	60°	60°
	6.6 m/s	−30° C., 6.6 m/s	Avg/0	Avg/0	B/50° C.	(MT11030	(Montana
Ex. No.	ft.-lbf	ft.-lbf	MPa	MPa	° C.	Texture)	Texture)
1*	38	35.8	2049	48	102.0	4.8	15.0
2	45.9	39.6	1593	47	133.5	7.4	33.0
3*	45.8	37.2	1971	47	117.6	11.9	13.9
4*	39	35.1	2241	51	113.4	5.2	12.2
5*	44.2	41.2	2444	63	111.6	6.1	17.3
6	39.1	33.7	2063	62	72.0	7.0	22.5
7*	34.3	35.3	1944	49	101.9	5.4	14.1
8	44.6	40	2085	48	96.6	7.4	32.4
9	43.6	42.4	2231	63	108.2	6.6	21.8
10	37.1	35.3	2133	49	110.1	6.4	18.6
11*	41.2	34.3	1983	46	124.4	6.0	16.5
12*	38.3	40.8	2270	53	109.2	5.0	12.7
13	38.6	39.7	1809	51	115.7	6.6	20.6
14*	38.9	33.2	1763	48	115.3	5.1	12.4
15*	35.9	32.8	1746	53	102.7	6.9	19.9
16*	38.9	36.6	2270	52	123.3	5.4	13.7
17	41.2	36.1	1887	49	114.0	7.2	13.7
18*	36.4	31	2555	63	56.3	5.7	16.2
19*	42.7	40.6	2628	63	110.1	5.7	14.8
20	40.4	38	2165	50	115.6	7.4	23.0
21*	45.1	35.6	2617	63	117.6	6.4	18.8
*Examples of the invention

The data in Tables 3 to 6 shows that the Examples of the invention (1, 3, 4, 5, 7, 11, 12, 14, 15, 16, 18, 19 and 21) comprising a blend of a polycarbonate and a co-polycarbonate, or the co-polycarbonate, along with the other resins, have the best balance of properties, including low gloss, high melt flow and high impact without significant sacrifice in other physical properties. The Examples having only a co-polycarbonate, but not both a polycarbonate and a co-polycarbonate, did not have a balance of properties that was as good, but did have higher melt flow than samples having polycarbonate only or the blend.

Additional Examples 22 to 33 were produced at various levels of components from Table 1. The formulations used are shown in Table 7 below. All amounts are in weight percent (wt. %).

TABLE 7
	PC-1	MBS	BABS	PC-Si	Co-poly 3	SAN
Ex. No.	wt. %	wt. %	wt %	wt. %	wt. %	wt. %
22	60	0	20	7.69	0	12.31
23	68	6	20	0	0	6
24*	0	0	20	7.69	60	12.31
25*	45	6	20	0	23	6
26*	0	6	20	0	68	6
27*	40	0	20	7.69	20	12.31
28	68	6	20	0	0	6
29*	20	0	20	7.69	40	12.31
20*	0	6	20	0	68	6
31*	0	0	20	7.69	60	12.31
32*	22	6	20	0	46	6
33*	60	0	20	7.69	0	12.31
*Examples of the invention

All of the above samples contained a stabilization package and color concentrate package. The color concentrate package was included in the stabilization package, and the stabilization package was added to the samples. The stabilization package contained 0.4 PETS; 0.5 hindered phenol AO; 0.2 Seenox™ 412 S (thio ester); 0.1 phosphite stabilizer; 0.3 UV stabilizer; 1.59 TiO₂; and 0.93 color concentrate package (all in parts per hundred (phr) polymer). The color concentrate package contained: 36.5 g carbon black; 2.5 g sol red 135; 202 g pigment yellow 183; 188 g pigment green 50; 71 g pigment blue 29; 2400 g PC powder (high flow PC, MW 22,000).

The samples from Table 7 were then tested according to the test methods described above. Results of the tests are shown in Tables 8 to 11 below.

TABLE 8
		MVR	Visc.
	MVR	260° C.,	Change
	260° C.,	5 kg,	after			ISO
	5 kg	18 min	30 min,	Flexural	Flexural	HDT at
Ex.	cm3/	cm3/	260° C.	Modulus	Strength	1.8 MPa
No.	10 min	10 min	%	MPa	MPa	° C.
22	28.2	38.1	−34	2535	91.4	98.6
23	17.32	23.8	−18	2290	86.0	101.9
24*	39	52.5	−37	2435	86.1	87.9
25*	19.65	26	−23	2372	85.7	99.6
26*	26.7	30.5	−24	2164	80.1	89.5
27*	27.9	37.4	−38	2331	84.8	97.1
28	15.56	16.51	−25	2424	89.4	105.0
29*	31.73	31.34	−36	2301	86.6	93.7
30*	26.32	26.19	−23	2288	83.7	91.1
31*	36.62	37.5	−34	2177	80.1	90.9
32*	21.34	22.18	−26	2252	82.6	94.7
33	24.45	25.46	−36	2309	86.4	100.1
*Examples of the invention

TABLE 9
	ISO		ISO		ISO		ISO
	Notched		Notched		Notched		Notched
	Izod		Izod		Izod		Izod
	Impact at	%	Impact at	%	Impact at	%	Impact at	%
	23° C.	Ductility	−20° C.	Ductility	−30° C.	Ductility	−40° C.	Ductility
Ex. No.	kJ/m2	%	kJ/m2	%	kJ/m2	%	kJ/m2	%
22	53.1	100	27.5	100	21.5	100	10.8	90
23	72.0	100	52.1	100	55.6	100	50.6	100
24*	68.3	100	44.3	100	34.5	100	26.2	90
25*	64.1	100	52.3	100	49.5	100	46.8	100
26*	48.9	100	44.5	100	44.1	100	45.0	100
27*	49.2	100	26.4	100	13.4	100	11.2	100
28	76.9	100	54.1	100	50.0	100	47.2	100
29*	61.0	100	41.4	100	22.8	100	13.8	100
30*	58.2	100	47.9	100	42.1	100	40.7	100
31*	68.8	100	46.5	100	29.9	100	21.7	90
32*	73.7	100	46.0	100	41.1	100	44.9	100
33	61.7	100	38.7	100	29.2	100	21.2	100
*Examples of the invention

TABLE 10
	Dyn.
	Energy to
	Max Load	%	Chord	Stress @	Vicat
Ex.	−30° C., 6.6 m/s	Ductility	Modulus	Yield	B/50, ° C.
No.	ft.-lbf	%	MPa	MPa	° C.
22	40	20	2661	56.7	117.2
23	42.3	100	2424	53.5	124.0
24*	40.3	0	2584	54.2	108.0
25*	38.1	100	2447	56.4	120.2
26*	39.9	100	2338	51.8	109.4
27*	44.2	0	2604	56.1	115.9
28	42.1	20	2497	55.3	128.2
29*	41.4	0	2538	54.9	112.4
30*	38.7	100	2543	54.2	108.9
31*	41.3	0	2557	54.0	108.2
32*	39.3	40	2562	54.4	114.1
33	36.3	0	2590	55.5	117.8
*Examples of the invention

TABLE 11
	Gloss at		Gloss at			Gloss at
	60°	Gloss at	60°		Gloss at	60°
	(Roch-	60°	(1055-	Gloss at	60°	(N111
Ex.	ester	(Montana	2	60° (N122	(MT11030	Tex-
No.	Texture	Texture)	Texture)	Texture)	Texture)	ture)
22	7.4	12.0	10.0	4.8	5.4	7.8
23	7.4	13.8	10.6	NA	5.6	7.9
24*	6.2	7.3	7.5	3.7	4.3	5.7
25*	7.2	9.8	9.6	4.7	5.4	8.0
26*	6.5	7.5	7.7	3.9	4.5	6.4
27*	7.1	8.9	NA	4.4	5.0	8.1
28	7.8	10.4	10.5	4.9	5.5	9.6
29*	7.1	7.9	7.9	4.1	4.7	6.9
30*	6.5	7.3	7.1	3.9	4.7	6.2
31*	6.5	7.1	7.0	3.9	4.4	5.6
32*	7.1	8.5	8.8	4.4	4.9	7.2
33	7.1	9.1	9.3	4.5	5.2	7.8
*Examples of the invention

The data in Tables 8 to 11 shows that the Examples of the invention (24, 25, 26, 27, 29, 30, 31 and 32) comprising a blend of a polycarbonate and a co-polycarbonate, or the co-polycarbonate, along with the other resins, have the best balance of properties, including low gloss, high melt flow and high impact, without sacrificing other physical properties. The Examples having only a co-polycarbonate, but not both, did not have a balance of properties that was as good, but did have higher flow than samples having polycarbonate only or the blend.

FIG. 1 is a plot of the predicted melt volume rate (MVR) versus the molecular weight of polycarbonate and the co-polycarbonate. The values reported in FIG. 1 are lines of constant melt flow and represent model predictions from a design space in which these compositions were systematically varied. As shown in FIG. 1, samples having only polycarbonate can only achieve an MVR up to about 45, while those having a blend of the polycarbonate and co-polycarbonate, or those with only the co-polycarbonate, can achieve a higher MVR, up to about 60. The plot is a response surface showing the relationship between composition and melt flow, using the data from the Examples in Table 2, as input into a statistical modeling package.

As used herein, “(meth)acrylate” is inclusive of both acrylates and methacrylates. Further, as used herein, the terms “first,” “second,” and the like do not denote any order or importance, but rather are used to distinguish one element from another, and the terms “the”, “a” and “an” do not denote a limitation of quantity, but rather denote the presence of at least one of the referenced item. All ranges disclosed herein for the same properties or amounts are inclusive of the endpoints, and each of the endpoints is independently combinable. All cited patents, patent applications, and other references are incorporated herein by reference in their entirety.

The modifier “about” used in connection with a quantity is inclusive of the stated value and has the meaning dictated by the context (that is, includes the degree of error associated with measurement of the particular quantity).

“Optional” or “optionally” means that the subsequently described event or circumstance may or may not occur, or that the subsequently identified material may or may not be present, and that the description includes instances where the event or circumstance occurs or where the material is present, and instances where the event or circumstance does not occur or the material is not present.

While the invention has been described with reference to a preferred embodiment, it will be understood by those skilled in the art that various changes may be made and equivalents may be substituted for elements thereof without departing from the scope of the invention. In addition, many modifications may be made to adapt a particular situation or material to the teachings of the invention without departing from essential scope thereof. Therefore, it is intended that the invention not be limited to the particular embodiment disclosed as the best mode contemplated for carrying out this invention, but that the invention will include all embodiments falling within the scope of the appended claims.

Claims

1. A thermoplastic composition comprising in combination an aliphatic/aromatic co-polycarbonate component; an impact modifier; and a rigid copolymer, wherein the aliphatic/aromatic co-polycarbonate comprises repeating carbonate units of the formula: in which at least about 60 percent of the total number of R1 groups are aromatic organic radicals and the balance thereof are aliphatic, alicyclic, or aromatic radicals; and repeating functional aliphatic units of the formula: X—R—X wherein R is a C1-C18 aliphatic radical or a C3-C18 cycloaliphatic radical, and each X is independently a hydroxyl, carboxyl, ester or acid chloride group selected from the following formulas: —OH; —R2OH; —COOH; —COOR2; and —COCl wherein each R2 is independently a C1-C18 monovalent hydrocarbon.

2. The composition of claim 1, wherein each X in the functional aliphatic compound has the formula —OH.

3. The composition of claim 2, wherein said functional aliphatic compound is selected from the group consisting of aliphatic diols and aliphatic polyols.

4. The composition of claim 3, wherein the functional aliphatic compound is neopentyl glycol or 1,4-butanediol.

5. The composition of claim 1, wherein the repeating functional aliphatic units have the formula:

6. The composition of claim 1, wherein the rigid copolymer is a vinyl aromatic copolymer.

7. The composition of claim 6, wherein the vinyl aromatic copolymer is SAN.

8. The composition of claim 1, further comprising a polycarbonate-polysiloxane copolymer.

9. The composition of claim 1, further comprising a polycarbonate component.

10. The composition of claim 9, wherein the ratio of polycarbonate component to co-polycarbonate component is from 1:99 to 50:50.

11. An article comprising the composition of claim 1.

12. The article of claim 11, wherein the article has a surface gloss level of less than 15 when measured on a textured surface according to ASTM D2457 at 60° using a Gardner Gloss Meter and 3 millimeter color chips.

13. The article of claim 12, wherein the article has a surface gloss level of less than 10 when measured on a textured surface according to ASTM D2457 at 60° using a Gardner Gloss Meter and 3 millimeter color chips.

14. The article of claim 12, wherein the textured surface is a commercially available textured surface selected from MT11030 (a fine texture); Montana Texture (a coarse texture); Rochester Texture; 1055-2 Texture; N122 Texture; and N111 Texture.

15. A thermoplastic composition comprising in combination an aliphatic/aromatic co-polycarbonate component; an impact modifier; and a rigid copolymer, wherein the aliphatic/aromatic co-polycarbonate comprises repeating carbonate units of the formula: in which at least about 60 percent of the total number of R1 groups are aromatic organic radicals and the balance thereof are aliphatic, alicyclic, or aromatic radicals; and repeating functional aliphatic units of the formula: X—R—X wherein R is a C1-C18 aliphatic radical or a C3-C18 cycloaliphatic radical, and each X is independently a hydroxyl, carboxyl, ester or acid chloride group selected from the following formulas: —OH; —R2OH; —COOH; —COOR2; and —COCl wherein each R is independently a C1-C18 monovalent hydrocarbon, and wherein the thermoplastic composition has a melt volume rate (MVR) of at least 13 cm3/10 minutes when measured at 260° C. using a 5-kilogram weight, with a six minute preheat, according to ASTM D1238.

16. The thermoplastic composition of claim 15, wherein the thermoplastic composition has a melt volume rate (MVR) of at least 20 cm3/10 minutes when measured at 260° C. using a 5-kilogram weight, with a six minute preheat, according to ASTM D1238.

17. The composition of claim 15, further comprising a polycarbonate-polysiloxane copolymer.

18. The composition of claim 15, further comprising a polycarbonate component.

19. The composition of claim 18, wherein the ratio of polycarbonate component to co-polycarbonate component is from 1:99 to 50:50.

20. The composition of claim 15, wherein the functional aliphatic compound is neopentyl glycol or 1,4-butanediol.

21. The composition of claim 15, wherein the repeating functional aliphatic units have the formula: