JP6073700B2 - Reinforced polycarbonate resin composition - Google Patents

Description

  The present invention relates to a reinforced polycarbonate resin composition comprising an aromatic polycarbonate resin, a liquid crystal polyester resin, and a fibrous reinforcing filler. More specifically, the present invention relates to a reinforced polycarbonate resin composition which is excellent in strength and moldability and particularly suitable for thin precision parts.

  Polycarbonate resin (hereinafter sometimes referred to as “PC resin”) is a resin excellent in heat resistance, impact resistance, dimensional stability, etc., and is in the electric / electronic parts field, mechanical parts field, automotive parts field, OA equipment. Widely used in the parts field. Further, a reinforced polycarbonate resin composition in which a reinforced filler is blended with a polycarbonate resin is used in a wide range of applications due to properties such as mechanical strength, dimensional stability, and flame retardancy. In recent years, there has been a remarkable tendency for products to be lighter, thinner, and shorter, for example, the outer shell parts have become extremely thin. Such a member is required to have a material having not only fluidity but also rigidity and strength higher than those of conventional members. In particular, bending strength and strength represented by bending strain are becoming more and more important with the diversification of usage environments represented by mobile terminal devices.

  Conventionally, as a method for achieving both rigidity and fluidity, a method of blending a thermoplastic resin, a reinforcing material, and a liquid crystal polyester resin exhibiting liquid crystallinity (hereinafter sometimes referred to as “LCP resin”) to simultaneously improve rigidity and fluidity Many have been proposed. Even in the case of PC resins, many attempts have been made to blend LCP resins into reinforced PC resin compositions.

  Patent Document 1 reports a glass fiber reinforced thermoplastic resin composition comprising LCP resin, glass fiber and / or glass flake, and PC resin obtained by a specific production method. This document describes that a high elastic modulus and good impact resistance can be achieved simultaneously.

  In Patent Document 2, PC resin, LCP resin, polytetrafluoroethylene mixture composed of polytetrafluoroethylene particles and organic polymer, flame retardant, fibrous inorganic reinforcing material, and flame retardant polycarbonate composed of phosphorus stabilizer Resin compositions have been reported. This document describes that in addition to flame retardancy, a high elastic modulus and good fluidity can be achieved simultaneously.

  Patent Document 3 reports a glass fiber reinforced polycarbonate resin composition comprising a PC resin, an LCP resin, and a reinforcing filler containing specific glass fibers. This document describes excellent rigidity, dimensional accuracy, fluidity, and reduction of mold wear during molding.

  Patent Document 4 reports a resin composition comprising a polyester-based resin that does not form an anisotropic molten phase, a liquid crystalline resin that can form an anisotropic molten phase, a phosphorus compound, and glass fibers that have been subjected to a specific treatment. Has been. This document describes a resin composition having high fluidity and rigidity and excellent toughness. However, there is no description regarding strength in any of these documents.

  In general, PC resin and LCP resin are incompatible, and in the composition as described above, although the rigidity is improved due to the low interfacial adhesion due to the incompatibility of PC resin and LCP resin, the strength is rather Therefore, in order to improve the strength, it is necessary to improve the compatibility between the PC resin and the LCP resin.

  As an example of improving the compatibility between PC resin and LCP resin, in Patent Document 5, in order to improve the compatibility between polypropylene and LCP resin, a reaction product is prepared by using LCP and maleic anhydride modified polypropylene with an extruder. Although the compatibility of the reaction product, polypropylene, and LCP resin is improved, it is different from the strength improvement effect of the present invention.

  Patent Document 6 reports the effect of improving rigidity, weld strength and impact resistance by melting and kneading PC resin, LCP resin, and diamine, and compatibilizing them. In addition, the thin-wall strength of the polycarbonate-rich composition is not sufficient.

  Patent Document 7 describes that a PC resin, an LCP resin, and a thermoplastic polyester resin are blended to control the dispersed particle size of the LCP resin, but for compatibilization, the thermoplastic polyester resin is an essential component. Yes, different from the present invention. There is no mention of strength.

  As described above, in the resin composition in which the LCP resin is blended with the reinforced PC resin composition, the compatibility between the PC resin and the LCP resin is improved, and it is expressed not only in rigidity and fluidity but also in bending strength and bending strain. There is no report to improve the strength.

Japanese Patent Application Laid-Open No. 07-258531 JP 2008-163315 A JP 2012-188578 A Japanese Patent No. 4920394 Japanese Patent No. 3648803 Japanese Patent No. 3248337 JP 2009-155377 A

  An object of the present invention is to provide a reinforced polycarbonate resin composition which is excellent in moldability, rigidity and strength and suitable for thin precision parts.

  As a result of intensive studies to solve such problems, the present inventors have found that in a reinforced polycarbonate resin composition comprising an aromatic polycarbonate resin, a liquid crystal polyester resin, and a fibrous reinforcing filler, one of the aromatic polycarbonate resin and the liquid crystal polyester resin is used. The reinforced polycarbonate resin composition whose part was transesterified was found to be a resin material that solves the above-mentioned problems, and further studies were made to complete the present invention. That is, according to the present invention, (1) (A) aromatic polycarbonate resin (component A) 98 to 60% by weight and (B) liquid crystal polyester resin (component B) 2 to 40% by weight of resin component 100 parts by weight On the other hand, in the reinforced polycarbonate resin composition comprising (C) 10 to 150 parts by weight of a fibrous reinforcing filler (C component) and (D) 0.001 to 2 parts by weight of a phosphorus stabilizer (D component), The content of alkali metal and / or alkaline earth metal contained in the component is in the range of 5 to 300 ppm, and part of component A and component B in the obtained resin composition is transesterified. A reinforced polycarbonate resin composition is provided.

One of the more preferable embodiments of the present invention is the above-mentioned constitution characterized in that (2) component B is a liquid crystal polyester resin polymerized using p-hydroxybenzoic acid and 6-hydroxy-2-naphthoic acid as raw materials. (1) The reinforced polycarbonate resin composition according to (1).
One of the more preferable embodiments of the present invention is the reinforced polycarbonate resin composition according to the above configuration (1) or (2), wherein the component (3) is a glass fiber.
One of the more preferable aspects of the present invention is that (4) the C component includes a flat cross-section glass fiber having an average value of the ratio of the major axis to the minor axis (major axis / minor axis) of the fiber section of 3.2 to 8. It is a reinforced polycarbonate resin composition according to the above constitution (3), which is a glass fiber.
One of the more preferable embodiments of the present invention is the reinforced polycarbonate resin composition according to the above constitution (1) or (2), wherein the component (5) is a carbon fiber.
One of the more preferable embodiments of the present invention is the above-mentioned constitutions (1) to (5), wherein (6) component D is a pentaerythritol diphosphite compound represented by the following general formula [1]. The reinforced polycarbonate resin composition according to any one of the above.

[Wherein A ¹ and A ² are each independently a hydrogen atom, an alkyl group having 1 to 20 carbon atoms, an aryl group or an alkylaryl group having 6 to 20 carbon atoms, an aralkyl group having 7 to 30 carbon atoms, or a carbon number. A group selected from the group consisting of 4 to 20 cycloalkyl groups and 2- (4-oxyphenyl) propyl-substituted aryl groups having 15 to 25 carbon atoms. In addition, the cycloalkyl group and the aryl group may be substituted with an alkyl group. ]

One of the more preferred embodiments of the present invention is (7) a mixture of component A and component B prepared by reacting (E) aromatic polycarbonate resin (component A) and liquid crystal polyester resin (component B) with an extruder. (E component), (A) polycarbonate resin (A component) and / or (B) liquid crystal polyester resin (B component), (C) reinforcing filler (C component) and (D) phosphorus stabilizer (D component) The reinforced polycarbonate resin composition according to any one of the above constitutions (1) to (6), wherein the resin composition is prepared by melt-kneading again.
One of the more preferable embodiments of the present invention is (8) the above-mentioned constitution (1) wherein the average fibril diameter of the B component remaining after the surface of the molded article is treated with hydrazine is 0.01 to 3 μm. ) To (7), the molded article made of the reinforced polycarbonate resin composition.

Hereinafter, the present invention will be specifically described.
(Component A: aromatic polycarbonate resin)
The aromatic polycarbonate resin used as the component A of the present invention is usually obtained by reacting a dihydroxy compound and a carbonate precursor by an interfacial polycondensation method or a melt transesterification method. It is obtained by polymerizing by an exchange method or polymerized by a ring-opening polymerization method of a cyclic carbonate compound. As a dihydroxy component used here, what is normally used as a dihydroxy component of an aromatic polycarbonate should just be used. Bisphenols are preferred as the main component of the dihydroxy component, but aliphatic diols can also be partly used as long as they do not impair the spirit of the present invention. Examples of bisphenols include 4,4′-dihydroxybiphenyl, bis (4-hydroxyphenyl) methane, 1,1-bis (4-hydroxyphenyl) ethane, and 1,1-bis (4-hydroxyphenyl) -1- Phenylethane, 2,2-bis (4-hydroxyphenyl) propane, 2,2-bis (4-hydroxy-3-methylphenyl) propane, 1,1-bis (4-hydroxyphenyl) -3,3,5 -Trimethylcyclohexane, 2,2-bis (4-hydroxy-3,3'-biphenyl) propane, 2,2-bis (4-hydroxy-3-isopropylphenyl) propane, 2,2-bis (3-t- Butyl-4-hydroxyphenyl) propane, 2,2-bis (4-hydroxyphenyl) butane, 2,2-bis (4-hydroxypheny) ) Octane, 2,2-bis (3-bromo-4-hydroxyphenyl) propane, 2,2-bis (3,5-dimethyl-4-hydroxyphenyl) propane, 2,2-bis (3-cyclohexyl-4) -Hydroxyphenyl) propane, 1,1-bis (3-cyclohexyl-4-hydroxyphenyl) cyclohexane, bis (4-hydroxyphenyl) diphenylmethane, 9,9-bis (4-hydroxyphenyl) fluorene, 9,9-bis (4-hydroxy-3-methylphenyl) fluorene, 1,1-bis (4-hydroxyphenyl) cyclohexane, 1,1-bis (4-hydroxyphenyl) cyclopentane, 4,4′-dihydroxydiphenyl ether, 4,4′-dihydroxy-3,3′-dimethyldiphenyl ether, 4,4′-sulfoni Diphenol, 4,4'-dihydroxydiphenyl sulfoxide, 4,4'-dihydroxydiphenyl sulfide, 2,2'-dimethyl-4,4'-sulfonyldiphenol, 4,4'-dihydroxy-3,3'-dimethyl Diphenyl sulfoxide, 4,4′-dihydroxy-3,3′-dimethyldiphenyl sulfide, 2,2′-diphenyl-4,4′-sulfonyldiphenol, 4,4′-dihydroxy-3,3′-diphenyldiphenyl sulfoxide 4,4′-dihydroxy-3,3′-diphenyldiphenyl sulfide, 1,3-bis {2- (4-hydroxyphenyl) propyl} benzene, 1,4-bis {2- (4-hydroxyphenyl) propyl } Benzene, 1,4-bis (4-hydroxyphenyl) cyclohexane, 1,3-bis (4-hydro Cyphenyl) cyclohexane, 4,8-bis (4-hydroxyphenyl) tricyclo [5.2.1.02,6] decane, 4,4 ′-(1,3-adamantanediyl) diphenol, 1,3-bis (4-Hydroxyphenyl) -5,7-dimethyladamantane etc. and the following general formula [2]

(In the above general formula [2], R ¹ and R ² are each independently an alkyl group having 1 to 10 carbon atoms, an alkoxy group having 1 to 10 carbon atoms, or a substituted or unsubstituted aryl having 6 to 15 carbon atoms. A substituted or unsubstituted aryloxy group having 6 to 15 carbon atoms, a substituted or unsubstituted aralkyl group having 7 to 15 carbon atoms, and a substituted or unsubstituted aralkyloxy group having 7 to 15 carbon atoms. , R ³ , R ⁴ , R ⁵ , R ⁶ , R ⁷ and R ⁸ are each independently a hydrogen atom, an alkyl group having 1 to 12 carbon atoms, or a substituted or unsubstituted aryl group having 6 to 12 carbon atoms. And a and b are natural numbers of 0 or 1 to 4, c + d is a natural number of 150 or less, and X is a divalent aliphatic group having 2 to 8 carbon atoms. Examples include bisphenol compounds It is.

  Examples of the aliphatic diols include 2,2-bis- (4-hydroxycyclohexyl) -propane, 1,14-tetradecanediol, octaethylene glycol, 1,16-hexadecanediol, 4,4′-bis (2- Hydroxyethoxy) biphenyl, bis {(2-hydroxyethoxy) phenyl} methane, 1,1-bis {(2-hydroxyethoxy) phenyl} ethane, 1,1-bis {(2-hydroxyethoxy) phenyl} -1- Phenylethane, 2,2-bis {(2-hydroxyethoxy) phenyl} propane, 2,2-bis {(2-hydroxyethoxy) -3-methylphenyl} propane, 1,1-bis {(2-hydroxyethoxy) ) Phenyl} -3,3,5-trimethylcyclohexane, 2,2-bis {4- (2-hydroxy) Ethoxy) -3,3′-biphenyl} propane, 2,2-bis {(2-hydroxyethoxy) -3-isopropylphenyl} propane, 2,2-bis {3-tert-butyl-4- (2-hydroxy) Ethoxy) phenyl} propane, 2,2-bis {(2-hydroxyethoxy) phenyl} butane, 2,2-bis {(2-hydroxyethoxy) phenyl} -4-methylpentane, 2,2-bis {(2 -Hydroxyethoxy) phenyl} octane, 1,1-bis {(2-hydroxyethoxy) phenyl} decane, 2,2-bis {3-bromo-4- (2-hydroxyethoxy) phenyl} propane, 2,2- Bis {3,5-dimethyl-4- (2-hydroxyethoxy) phenyl} propane, 2,2-bis {3-cyclohexyl-4- (2-hydroxyethyl) Xyl) phenyl} propane, 1,1-bis {3-cyclohexyl-4- (2-hydroxyethoxy) phenyl} cyclohexane, bis {(2-hydroxyethoxy) phenyl} diphenylmethane, 9,9-bis {(2-hydroxy) Ethoxy) phenyl} fluorene, 9,9-bis {4- (2-hydroxyethoxy) -3-methylphenyl} fluorene, 1,1-bis {(2-hydroxyethoxy) phenyl} cyclohexane, 1,1-bis { (2-hydroxyethoxy) phenyl} cyclopentane, 4,4′-bis (2-hydroxyethoxy) diphenyl ether, 4,4′-bis (2-hydroxyethoxy) -3,3′-dimethyldiphenyl ether Ter, 1,3-bis [2-{(2-hydroxyethoxy) phenyl} propyl] benzene, 1 , 4-bis [2-{(2-hydroxyethoxy) phenyl} propyl] benzene, 1,4-bis {(2-hydroxyethoxy) phenyl} cyclohexane, 1,3-bis {(2-hydroxyethoxy) phenyl} Cyclohexane, 4,8-bis {(2-hydroxyethoxy) phenyl} tricyclo [5.2.1.02,6] decane, 1,3-bis {(2-hydroxyethoxy) phenyl} -5,7-dimethyl Adamantane, 3,9-bis (2-hydroxy-1,1-dimethylethyl) -2,4,8,10-tetraoxaspiro (5,5) undecane, 1,4: 3,6-dianhydro-D-sorbitol (Isosorbide), 1,4: 3,6-dianhydro-D-mannitol (isomannide), 1,4: 3,6-dianhydro-L-iditol Isoidide), and the like.

  Among these, aromatic bisphenols are preferable, and among them, 1,1-bis (4-hydroxyphenyl) -1-phenylethane, 2,2-bis (4-hydroxyphenyl) propane, 2,2-bis (4 -Hydroxy-3-methylphenyl) propane, 1,1-bis (4-hydroxyphenyl) cyclohexane, 1,1-bis (4-hydroxyphenyl) -3,3,5-trimethylcyclohexane, 4,4'-sulfonyl Diphenol, 2,2′-dimethyl-4,4′-sulfonyldiphenol, 9,9-bis (4-hydroxy-3-methylphenyl) fluorene, 1,3-bis {2- (4-hydroxyphenyl) Propyl} benzene and 1,4-bis {2- (4-hydroxyphenyl) propyl} benzene, particularly 2,2-bis 4-hydroxyphenyl) propane, 1,1-bis (4-hydroxyphenyl) cyclohexane, 4,4′-sulfonyldiphenol, 9,9-bis (4-hydroxy-3-methylphenyl) fluorene and the above general formula [ 2] is preferable. Among them, 2,2-bis (4-hydroxyphenyl) propane having excellent strength and good durability is most preferable. Moreover, you may use these individually or in combination of 2 or more types.

  The aromatic polycarbonate resin used as the component A of the present invention may be a branched polycarbonate resin using a branching agent in combination with the dihydroxy compound. Examples of the trifunctional or higher polyfunctional aromatic compound used in the branched polycarbonate resin include phloroglucin, phloroglucid, or 4,6-dimethyl-2,4,6-tris (4-hydroxydiphenyl) heptene-2, 2 , 4,6-trimethyl-2,4,6-tris (4-hydroxyphenyl) heptane, 1,3,5-tris (4-hydroxyphenyl) benzene, 1,1,1-tris (4-hydroxyphenyl) Ethane, 1,1,1-tris (3,5-dimethyl-4-hydroxyphenyl) ethane, 2,6-bis (2-hydroxy-5-methylbenzyl) -4-methylphenol, 4- {4- [ Trisphenol such as 1,1-bis (4-hydroxyphenyl) ethyl] benzene} -α, α-dimethylbenzylphenol, tetra (4-hydride) Loxyphenyl) methane, bis (2,4-dihydroxyphenyl) ketone, 1,4-bis (4,4-dihydroxytriphenylmethyl) benzene, or trimellitic acid, pyromellitic acid, benzophenonetetracarboxylic acid and their acids Among them, 1,1,1-tris (4-hydroxyphenyl) ethane and 1,1,1-tris (3,5-dimethyl-4-hydroxyphenyl) ethane are preferable. 1-Tris (4-hydroxyphenyl) ethane is preferred.

  These aromatic polycarbonate resins are produced by a reaction means known per se for producing an ordinary aromatic polycarbonate resin, for example, a method of reacting an aromatic dihydroxy component with a carbonate precursor such as phosgene or carbonic acid diester. The basic means of the manufacturing method will be briefly described.

  In a reaction using, for example, phosgene as a carbonate precursor, the reaction is usually performed in the presence of an acid binder and a solvent. As the acid binder, for example, an alkali metal hydroxide such as sodium hydroxide or potassium hydroxide or an amine compound such as pyridine is used. As the solvent, for example, halogenated hydrocarbons such as methylene chloride and chlorobenzene are used. In order to accelerate the reaction, a catalyst such as a tertiary amine or a quaternary ammonium salt can also be used. In that case, reaction temperature is 0-40 degreeC normally, and reaction time is several minutes-5 hours. The transesterification reaction using a carbonic acid diester as a carbonate precursor is performed by a method in which an aromatic dihydroxy component in a predetermined ratio is stirred with a carbonic acid diester while heating with an inert gas atmosphere to distill the generated alcohol or phenols. . The reaction temperature varies depending on the boiling point of the alcohol or phenol produced, but is usually in the range of 120 to 300 ° C. The reaction is completed while distilling off the alcohol or phenol produced under reduced pressure from the beginning. Moreover, in order to accelerate | stimulate reaction, the catalyst normally used for transesterification can also be used. Examples of the carbonic acid diester used in the transesterification include diphenyl carbonate, dinaphthyl carbonate, bis (diphenyl) carbonate, dimethyl carbonate, diethyl carbonate, and dibutyl carbonate. Of these, diphenyl carbonate is particularly preferred.

  In the present invention, a terminal terminator is used in the polymerization reaction. The end terminator is used for molecular weight control, and the obtained polycarbonate resin is excellent in thermal stability as compared with the other one because the end is blocked. Examples of the terminal terminator include monofunctional phenols represented by the following general formulas [3] to [5].

[In the formula, A is an alkyl group having 1 to 10 carbon atoms, a substituted or unsubstituted aryl group having 6 to 15 carbon atoms, a substituted or unsubstituted aralkyl group having 7 to 15 carbon atoms, and r is 0. -5, preferably an integer of 0-1. ]

[Wherein, n is an integer having 1 to 50 carbon atoms. ]

[Wherein, W is —R—O—, —R—CO—O— or —R—O—CO—, wherein R is a single bond or a carbon number of 1 to 10, preferably 1 to 5; Represents a valent aliphatic hydrocarbon group, and n is an integer of 1 to 50. ]

  Specific examples of the monofunctional phenols represented by the general formula [3] include, for example, phenol, isopropylphenol, p-tert-butylphenol, p-cresol, p-cumylphenol, 2-phenylphenol, 4-phenyl. Phenol, isooctylphenol, etc. are mentioned. The monofunctional phenols represented by the general formulas [4] to [5] are phenols having a long-chain alkyl group or an aliphatic ester group as a substituent, and using these, the terminal of the polycarbonate resin is used. These not only function as a terminal terminator or molecular weight regulator, but also improve the melt fluidity of the resin and facilitate molding, as well as reducing the water absorption rate of the resin. used. The substituted phenols represented by the general formula [4] preferably have n of 10 to 30, particularly 10 to 26. Specific examples thereof include decylphenol, dodecylphenol, tetradecylphenol, hexadecylphenol, octadecylphenol, Examples include eicosylphenol, docosylphenol, and triacontylphenol. The substituted phenols of the general formula [5] are preferably compounds in which W is —R—CO—O— and R is a single bond, and those in which n is 10 to 30, particularly 10 to 26 are suitable. Specific examples thereof include decyl hydroxybenzoate, dodecyl hydroxybenzoate, tetradecyl hydroxybenzoate, hexadecyl hydroxybenzoate, eicosyl hydroxybenzoate, docosyl hydroxybenzoate and triacontyl hydroxybenzoate. Among these monofunctional phenols, monofunctional phenols represented by the above general formula [3] are preferable, more preferably alkyl-substituted or phenylalkyl-substituted phenols, particularly preferably p-tert-butylphenol, p -Cumylphenol or 2-phenylphenol. These monofunctional phenolic terminal terminators are desirably introduced at the terminal at least 5 mol%, preferably at least 10 mol%, based on all the terminals of the obtained polycarbonate resin. Or a mixture of two or more thereof.

  The aromatic polycarbonate resin used as the component A of the present invention is a polyester carbonate obtained by copolymerizing an aromatic dicarboxylic acid, for example, terephthalic acid, isophthalic acid, naphthalenedicarboxylic acid or a derivative thereof, within the range not impairing the gist of the present invention. May be.

The viscosity average molecular weight of the aromatic polycarbonate resin used as the component A of the present invention is preferably in the range of 12,000 to 50,000, more preferably 12,000 to 30,000, and 12,000 to 25,000. A range is even more preferred, with a range of 15,000 to 25,000 being most preferred.
If the molecular weight exceeds 50,000, the melt viscosity becomes too high and the moldability may be inferior, and if the molecular weight is less than 12,000, there may be a problem in mechanical strength. In addition, the viscosity average molecular weight as used in the field of this invention was calculated | required and calculated | required first using the Ostwald viscometer from the solution which melt | dissolved the polycarbonate resin 0.7g in 20 ml of methylene chloride in the specific viscosity computed by following Formula. The viscosity average molecular weight M is determined by inserting the specific viscosity by the following formula.
Specific viscosity (η _SP ) = (t−t ₀ ) / t ₀
[T ₀ is methylene chloride falling seconds, t is sample solution falling seconds]
η _SP /c=[η]+0.45×[η] ² c (where [η] is the intrinsic viscosity)
[Η] = 1.23 × 10 ⁻⁴ M ^0.83
c = 0.7

  The polycarbonate resin used as the component A of the present invention has a total Cl (chlorine) amount in the resin of preferably 0 to 200 ppm, more preferably 0 to 150 ppm. If the total Cl content in the polycarbonate resin exceeds 200 ppm, the hue and thermal stability deteriorate, which is not preferable.

(B component: Liquid crystalline polyester resin)
The liquid crystal polyester resin used as the component B of the present invention is a thermotropic liquid crystal polyester resin and has a property that polymer molecular chains are aligned in a certain direction in a molten state. The arrangement state may be any of nematic, smectic, cholesteric, and discotic, and may exhibit two or more forms. Furthermore, the structure of the liquid crystal polyester resin may be any structure such as a main chain type, a side chain type, and a rigid main chain bent side chain type, but a main chain type liquid crystal polyester resin is preferred.

  The form of the arrangement state, that is, the property of the anisotropic molten phase can be confirmed by a conventional polarization inspection method using an orthogonal polarizer. More specifically, the anisotropic molten phase can be confirmed by using a Leitz polarizing microscope and observing a molten sample placed on a Leitz hot stage at a magnification of 40 times in a nitrogen atmosphere. When inspected between crossed polarizers, the polymer of the present invention transmits polarized light and exhibits optical anisotropy even in a molten stationary state.

  Further, the heat resistance of the liquid crystal polyester resin may be in any range, but it is appropriate that the liquid crystal polyester resin melts at a portion close to the processing temperature of the polycarbonate resin to form a liquid crystal phase. In this respect, it is more preferable that the deflection temperature under load of the liquid crystal polyester resin is 150 to 280 ° C, preferably 180 to 250 ° C. Such liquid crystal polyester resins belong to the so-called heat-resistant category II. In the case of such heat resistance, excellent moldability is achieved as compared with type I having higher heat resistance, and good flame retardancy is achieved as compared with type III having lower heat resistance.

  The liquid crystal polyester resin used as the component B of the present invention preferably contains a polyester unit and a polyesteramide unit, preferably an aromatic polyester resin and an aromatic polyesteramide resin, and contains an aromatic polyester unit and an aromatic polyesteramide unit. A liquid crystal polyester resin partially contained in the same molecular chain is also a preferred example.

Particularly preferred are wholly aromatic polyester resins and wholly aromatic polyester amides having unit constituents derived from one or more compounds selected from the group consisting of aromatic hydroxycarboxylic acids, aromatic hydroxyamines and aromatic diamines. Resin. More specifically,
1) a liquid crystal polyester resin synthesized from one or more compounds selected from the group consisting of aromatic hydroxycarboxylic acids and derivatives thereof;
2) Mainly a) One or more compounds selected from the group consisting of aromatic hydroxycarboxylic acids and derivatives thereof, b) 1 selected from the group consisting of aromatic dicarboxylic acids, alicyclic dicarboxylic acids and derivatives thereof A liquid crystal polyester resin synthesized from one or more compounds selected from the group consisting of a species or two or more compounds, and c) an aromatic diol, an alicyclic diol, an aliphatic diol and derivatives thereof,
3) Mainly a) One or more compounds selected from the group consisting of aromatic hydroxycarboxylic acids and derivatives thereof, b) One type selected from the group consisting of aromatic hydroxyamines, aromatic diamines and derivatives thereof, or A liquid crystal polyesteramide resin synthesized from two or more compounds, and c) one or two or more compounds selected from the group consisting of aromatic dicarboxylic acids, alicyclic dicarboxylic acids and derivatives thereof,
4) Mainly a) One or more compounds selected from the group consisting of aromatic hydroxycarboxylic acids and derivatives thereof, b) One type selected from the group consisting of aromatic hydroxyamines, aromatic diamines and derivatives thereof, or Two or more compounds, c) one or more compounds selected from the group consisting of aromatic dicarboxylic acids, alicyclic dicarboxylic acids and derivatives thereof, and d) aromatic diols, alicyclic diols, aliphatics Examples thereof include liquid crystal polyesteramide resins synthesized from one or more compounds selected from the group consisting of diols and derivatives thereof. 1) 1 selected mainly from the group consisting of aromatic hydroxycarboxylic acids and derivatives thereof. A liquid crystal polyester resin synthesized from two or more species is preferred.
Furthermore, you may use a molecular weight modifier together with said structural component as needed.

  Preferable examples of specific compounds used for the synthesis of the liquid crystal polyester resin used as the B component of the present invention include 2,6-naphthalenedicarboxylic acid, 2,6-dihydroxynaphthalene, 1,4-dihydroxynaphthalene and 6-hydroxy. 2-naphthalene compounds such as naphthoic acid, biphenyl compounds such as 4,4′-diphenyldicarboxylic acid, 4,4′-dihydroxybiphenyl, p-hydroxybenzoic acid, terephthalic acid, hydroquinone, p-aminophenol and p-phenylene Para-substituted benzene compounds such as diamines and their nuclear-substituted benzene compounds (substituent is selected from chlorine, bromine, methyl, phenyl, 1-phenylethyl), meta-substituted benzene compounds such as isophthalic acid, resorcin, And the following general formula [6], [7] or [8] A compound represented. Among these, p-hydroxybenzoic acid and 6-hydroxy-2-naphthoic acid are particularly preferable, and a liquid crystal polyester resin obtained by mixing both is preferable. As for the ratio of both, the range of 90-50 mol% is preferable for the former, The range of 80-65 mol% is more preferable, The range of 10-50 mol% is preferable for the latter, The range of 20-35 mol% is more preferable.

(Y is a group selected from the group consisting of an alkylene group having 1 to 4 carbon atoms and an alkylidene group, —O—, —SO—, —SO ₂ —, —S—, and —CO—, and Z is It is a group selected from the group consisting of — (CH ₂ ) _n — (n = 1 to 4) and —O (CH ₂ ) _n O— (n = 1 to 4).

  In addition, the liquid crystalline polyester resin used as the B component of the present invention may contain a polyalkylene terephthalate-derived unit that does not partially exhibit an anisotropic molten phase in the same molecular chain in addition to the above-described constituent components. . In this case, the alkylene group has 2 to 4 carbon atoms.

  The liquid crystal polyester resin used as the component B of the present invention contains 5-300 ppm of alkali metal and / or alkaline earth metal in the resin. The content is preferably in the range of 10 to 150 ppm, more preferably in the range of 10 to 100 ppm, and still more preferably in the range of 20 to 80 ppm. When the content of the alkali metal and / or alkaline earth metal is less than 5 ppm, the transesterification of the A component and the B component does not proceed, and when it exceeds 300 ppm, the decomposition reaction proceeds during the melt-kneading.

  The content of alkali metal and / or alkaline earth metal in the liquid crystal polyester resin was quantified by inductively coupled plasma emission spectroscopy (ICP-AES). Specifically, after thermal decomposition of the liquid crystalline polyester resin with sulfuric acid and nitric acid, the volume is determined with ultrapure water to prepare a test solution, and ICP-AES is used for elemental determination of alkali metal and / or alkaline earth metal in the test solution. Analysis was carried out.

  The basic production method of the liquid crystal polyester resin used as the component B in the present invention is not particularly limited, and can be produced according to a known polycondensation method of a liquid crystal polyester resin. The liquid crystalline polyester resin also has a logarithmic viscosity of at least about 2.0 dl / g, such as about 2.0-10.0 dl / g when dissolved in pentafluorophenol at 60% at a concentration of 0.1% by weight ( IV values) are generally indicated.

  In the reinforced polycarbonate resin composition of the present invention, it is necessary that the polycarbonate resin forms a continuous layer and the liquid crystal polyester resin forms a dispersed layer, respectively.

  Content of B component is 2-40 weight% in 100 weight% of resin components, 5-40 weight% is preferable, 5-30 weight% is more preferable, 5-20 weight% is further more preferable, 8% by weight is most preferred. When the content of the B component is not within the above range, the effect of transesterification of the A component and the B component is not exhibited, which is not preferable.

The reinforced polycarbonate resin composition of the present invention is characterized in that a part of the A component and the B component used in the present invention are transesterified. Here, the partial transesterification means that the transesterification rate calculated by the following method is 0.01% or more. As for A component and B component, the range of 0.01 to 50% is preferable, the range of 0.01 to 10% is more preferable, the range of 0.01 to 5% is further more preferable, and 0.01 to 1% is particularly preferable, and 0.01 to 0.5% is most preferable. When the A component and the B component are not transesterified, the compatibility of the polycarbonate resin and the liquid crystalline polyester resin is poor, causing phase separation, and the strength and strain in the bending test are not improved. The rigidity it has may be lost. In addition, the transesterification rate defined by this invention is computed by a following formula by < ¹ > H-NMR measurement.
Transesterification rate (%) = 100 × (integral ratio calculated from peak derived from transesterification reaction product) / (integral ratio calculated from peak derived from transesterification reaction product + integral ratio calculated from peak derived from polycarbonate resin)

(C component: fibrous reinforcing filler)
As the fibrous reinforcing filler used as the component C of the present invention, glass fiber, carbon fiber, metal fiber, asbestos, rock wool, ceramic fiber, slag fiber, potassium titanate whisker, boron whisker, aluminum borate whisker, carbonic acid Calcium whiskers, titanium oxide whiskers, and fibers obtained by surface-coating a dissimilar material such as metal with respect to these reinforcing agents can be mentioned, and two or more of these can also be used in combination.

Of these fibrous reinforcing fillers, glass fibers and carbon fibers are preferred. As for the glass fiber, a glass fiber having a flat fiber cross section is preferably used, and the average value of the ratio of the major axis to the minor axis (major axis / minor axis) of the fiber section is preferably 3.2 to 8. 2-6 are more preferable and 3.8-6 are still more preferable.
Glass fiber and carbon fiber can be selected from, for example, long fiber type (roving), short fiber chopped strand, milled fiber, and the like. In the milled fiber, the number average aspect ratio is preferably 5 or more.

  The fibrous reinforcing filler used as the component C of the present invention includes a sizing agent (eg, polyvinyl acetate, urethane, acrylic, polyester sizing agent, etc.), a coupling agent (eg, alkylalkoxysilane, polyorganohydrogensiloxane, etc.). A silane compound, a boron compound, a titanium compound, etc.) and other surface treatment agents. Examples of such other surface treatment agents include higher fatty acid esters, acid compounds (for example, phosphorous acid, phosphoric acid, carboxylic acid, and carboxylic acid anhydride), and waxes. Furthermore, it may be granulated with a sizing agent such as various resins, higher fatty acid esters, and waxes.

  The content of the fibrous reinforcing filler used as the C component of the present invention is 10 to 150 parts by weight, preferably 20 to 150 parts by weight, with respect to 100 parts by weight of the resin component from the A component and the B component. 20-100 weight part is more preferable, and 40-100 weight part is further more preferable. When the content is less than 10 parts by weight, the rigidity is not improved, and when it exceeds 150 parts by weight, the moldability is inferior.

(D component: phosphorus stabilizer)
Examples of phosphorus stabilizers used as the D component of the present invention include phosphite compounds, phosphonite compounds, phosphinite compounds, phosphine compounds, phosphate compounds, phosphonate compounds, phosphinate compounds, phosphine oxide compounds, phosphazene compounds, and the like. Of these, phosphite compounds are preferred.

  Examples of the phosphite compound include triphenyl phosphite, tris (nonylphenyl) phosphite, tridecyl phosphite, trioctyl phosphite, trioctadecyl phosphite, didecyl monophenyl phosphite, dioctyl monophenyl phosphite, diisopropyl Monophenyl phosphite, monobutyl diphenyl phosphite, monodecyl diphenyl phosphite, monooctyl diphenyl phosphite, tris (diethylphenyl) phosphite, tris (di-iso-propylphenyl) phosphite, tris (di-n-butyl) Phenyl) phosphite, tris (2,4-di-tert-butylphenyl) phosphite, tris (2,6-di-tert-butylphenyl) phosphite, distearyl Taerythritol diphosphite, bis (2,4-di-tert-butylphenyl) pentaerythritol diphosphite, bis (2,6-di-tert-butyl-4-methylphenyl) pentaerythritol diphosphite, bis ( 2,6-di-tert-butyl-4-ethylphenyl) pentaerythritol diphosphite, bis {2,4-bis (1-methyl-1-phenylethyl) phenyl} pentaerythritol diphosphite, phenylbisphenol A penta Examples include erythritol diphosphite, bis (nonylphenyl) pentaerythritol diphosphite, and dicyclohexylpentaerythritol diphosphite.

  Further, as other phosphite compounds, those which react with dihydric phenols and have a cyclic structure can be used. For example, 2,2′-methylenebis (4,6-di-tert-butylphenyl) (2,4-di-tert-butylphenyl) phosphite, 2,2′-methylenebis (4,6-di-tert- Examples include butylphenyl) (2-tert-butyl-4-methylphenyl) phosphite and 2,2-methylenebis (4,6-di-tert-butylphenyl) octyl phosphite.

  Among such phosphite compounds, a pentaerythritol diphosphite compound represented by the following general formula [1] is preferable, and distearyl pentaerythritol diphosphite and bis (2,4-di-tert-butylphenyl) pentaerythritol di Phosphite, bis (2,6-di-tert-butyl-4-methylphenyl) pentaerythritol diphosphite is particularly preferred.

[Wherein A ¹ and A ² are each independently a hydrogen atom, an alkyl group having 1 to 20 carbon atoms, an aryl group or an alkylaryl group having 6 to 20 carbon atoms, an aralkyl group having 7 to 30 carbon atoms, or a carbon number. A group selected from the group consisting of 4 to 20 cycloalkyl groups and 2- (4-oxyphenyl) propyl-substituted aryl groups having 15 to 25 carbon atoms. In addition, the cycloalkyl group and the aryl group may be substituted with an alkyl group. ]

  The content of the phosphorus stabilizer used as the D component of the present invention is 0.001 to 2 parts by weight, preferably 0.001 to 1 part by weight per 100 parts by weight of the total of the A component and the B component. 0.001-0.5 weight part is more preferable. When content of D component does not exist in the said range, the fusion heat stability of a reinforced polycarbonate resin composition, a bending test, and a moldability are inferior.

(Other ingredients)
In addition, the reinforced polycarbonate resin composition of the present invention can be blended with various flame retardants, reinforcing fillers, and additives that are usually blended with the polycarbonate resin as long as the effects of the present invention are not impaired.
Examples of such additives include hindered phenol stabilizers, ultraviolet absorbers, dyes and pigments, heat stabilizers, and antistatic agents.

(Flame retardants)
The reinforced polycarbonate resin composition of the present invention may be blended with various compounds known as flame retardants for flame retardant polycarbonate resins. The compounding of such a compound brings about an improvement in flame retardancy, but besides that, based on the properties of each compound, for example, an improvement in antistatic property, fluidity, rigidity and thermal stability is brought about. Examples of such flame retardants include (i) organic metal salt flame retardants (for example, organic sulfonate alkali (earth) metal salts, organic borate metal salt flame retardants, organic stannate metal salt flame retardants, etc.), ii) organophosphorous flame retardants (for example, organic group-containing monophosphate compounds, phosphate oligomer compounds, phosphonate oligomer compounds, phosphonitrile oligomer compounds, phosphonic acid amide compounds, etc.), (iii) silicone flame retardants comprising silicone compounds (Iv) fibrillated PTFE, among which organometallic salt flame retardants and organic phosphorus flame retardants are preferred.

(I) Organometallic salt flame retardant An organometallic salt flame retardant is an alkali (earth) metal salt of an organic acid having 1 to 50 carbon atoms, preferably 1 to 40 carbon atoms, preferably an alkali organic sulfonate (earth). A metal salt is preferred. The alkali (earth) metal salt of the organic sulfonate includes a fluorine-substituted alkyl sulfone such as a metal salt of a perfluoroalkyl sulfonic acid having 1 to 10, preferably 2 to 8 carbon atoms and an alkali metal or an alkaline earth metal. Metal salts of acids and metal salts of aromatic sulfonic acids having 7 to 50 carbon atoms, preferably 7 to 40 carbon atoms, and alkali metals or alkaline earth metals are included.

  Examples of the alkali metal constituting the metal salt include lithium, sodium, potassium, rubidium and cesium, and examples of the alkaline earth metal include beryllium, magnesium, calcium, strontium and barium. More preferred is an alkali metal. Among such alkali metals, rubidium and cesium having larger ionic radii are suitable when the requirement for transparency is higher, but these are not general-purpose and difficult to purify, resulting in cost. It may be disadvantageous. On the other hand, metals with smaller ionic radii such as lithium and sodium may be disadvantageous in terms of flame retardancy. Considering these, the alkali metal in the sulfonic acid alkali metal salt can be properly used. In any respect, the sulfonic acid potassium salt having an excellent balance of properties is most preferable. Such potassium salts and sulfonic acid alkali metal salts comprising other alkali metals can be used in combination.

  Specific examples of alkali metal perfluoroalkyl sulfonates include potassium trifluoromethane sulfonate, potassium perfluorobutane sulfonate, potassium perfluorohexane sulfonate, potassium perfluorooctane sulfonate, sodium pentafluoroethane sulfonate, perfluoro Sodium butanesulfonate, sodium perfluorooctanesulfonate, lithium trifluoromethanesulfonate, lithium perfluorobutanesulfonate, lithium perfluoroheptanesulfonate, cesium trifluoromethanesulfonate, cesium perfluorobutanesulfonate, perfluorooctanesulfonate Cesium, cesium perfluorohexane sulfonate, rubidium perfluorobutane sulfonate, and perf Oro hexane sulfonate rubidium, and these may be used in combination of at least one or two. Here, the carbon number of the perfluoroalkyl group is preferably in the range of 1-18, more preferably in the range of 1-10, and still more preferably in the range of 1-8. Of these, potassium perfluorobutanesulfonate is particularly preferred.

The alkali (earth) metal salt of perfluoroalkylsulfonic acid composed of an alkali metal is usually mixed with not less than fluoride ions (F ⁻ ). The presence of such fluoride ions can be a factor that lowers the flame retardancy, so it is preferably reduced as much as possible. The ratio of such fluoride ions can be measured by ion chromatography. The content of fluoride ions is preferably 100 ppm or less, more preferably 40 ppm or less, and particularly preferably 10 ppm or less. Moreover, it is suitable that it is 0.2 ppm or more in terms of production efficiency. Such alkali (earth) metal salt of perfluoroalkylsulfonic acid having a reduced amount of fluoride ion is contained in a raw material when producing a fluorine-containing organometallic salt using a known production method. A method for reducing the amount of fluoride ions, a method for removing hydrogen fluoride and the like obtained by the reaction by a gas generated during the reaction or heating, and a purification method such as recrystallization and reprecipitation for producing a fluorine-containing organometallic salt Can be produced by a method of reducing the amount of fluoride ions using, for example. In particular, organic metal salt flame retardants are relatively soluble in water, and therefore ion-exchanged water, especially water that has an electric resistance of 18 MΩ · cm or more, that is, an electric conductivity of about 0.55 μS / cm or less is used. In addition, it is preferable to produce by a process of dissolving at a temperature higher than room temperature and washing, then cooling and recrystallization.

  Specific examples of the aromatic (earth) metal salt of an aromatic sulfonate include, for example, disodium diphenyl sulfide-4,4′-disulfonate, dipotassium diphenyl sulfide-4,4′-disulfonate, potassium 5-sulfoisophthalate, Sodium 5-sulfoisophthalate, polysodium polyethylene terephthalate polysulfonate, calcium 1-methoxynaphthalene-4-sulfonate, disodium 4-dodecylphenyl ether disulfonate, polysodium poly (2,6-dimethylphenylene oxide) polysulfonate Poly (1,3-phenylene oxide) polysulfonic acid polysodium, poly (1,4-phenylene oxide) polysulfonic acid polysodium, poly (2,6-diphenylphenylene oxide) polysulfonic acid poly Lithium, poly (2-fluoro-6-butylphenylene oxide) polysulfonate, potassium sulfonate of benzenesulfonate, sodium benzenesulfonate, strontium benzenesulfonate, magnesium benzenesulfonate, dipotassium p-benzenedisulfonate, naphthalene-2 , 6-disulfonic acid dipotassium, biphenyl-3,3'-disulfonic acid calcium, diphenylsulfone-3-sulfonic acid sodium, diphenylsulfone-3-sulfonic acid potassium, diphenylsulfone-3,3'-disulfonic acid dipotassium, diphenylsulfone -3,4'-dipotassium disulfonate, α, α, α-trifluoroacetophenone-4-sodium sulfonate, dipotassium benzophenone-3,3'-disulfonate, thiof 2,5-disulfonic acid disodium, thiophene-2,5-disulfonic acid dipotassium, thiophene-2,5-disulfonic acid calcium, benzothiophene sodium sulfonate, diphenyl sulfoxide-4- potassium sulfonate, naphthalene sulfone Examples thereof include a formalin condensate of sodium acid and a formalin condensate of sodium anthracene sulfonate. Among these aromatic sulfonate alkali (earth) metal salts, potassium salts are particularly preferable. Among these aromatic sulfonate alkali (earth) metal salts, potassium diphenylsulfone-3-sulfonate and dipotassium diphenylsulfone-3,3′-disulfonate are preferable, and particularly a mixture thereof (the former and the latter). Is preferably 15/85 to 30/70).

  Preferable examples of the organic metal salt other than the alkali (earth) metal sulfonate include an alkali (earth) metal salt of a sulfate ester and an alkali (earth) metal salt of an aromatic sulfonamide. Examples of alkali (earth) metal salts of sulfates include alkali (earth) metal salts of sulfates of monovalent and / or polyhydric alcohols, and such monovalent and / or polyhydric alcohols. Examples of sulfuric acid esters include methyl sulfate, ethyl sulfate, lauryl sulfate, hexadecyl sulfate, polyoxyethylene alkylphenyl ether sulfate, pentaerythritol mono-, di-, tri-, tetra-sulfate, and lauric acid monoglyceride sulfate. Examples include esters, sulfates of palmitic acid monoglyceride, and sulfates of stearic acid monoglyceride. The alkali (earth) metal salts of these sulfates are preferably alkali (earth) metal salts of lauryl sulfate.

Alkali (earth) metal salts of aromatic sulfonamides include, for example, saccharin, N- (p-tolylsulfonyl) -p-toluenesulfonimide, N- (N′-benzylaminocarbonyl) sulfanilimide, and N- ( And an alkali (earth) metal salt of phenylcarboxyl) sulfanilimide.
The content of the organometallic salt-based flame retardant is preferably 0.001 to 1 part by weight, more preferably 0.005 to 0.5 part by weight, further preferably 100 parts by weight of the total of the A component and the B component. Is 0.01 to 0.3 parts by weight, particularly preferably 0.03 to 0.15 parts by weight.

(Ii) Organophosphorus Flame Retardant As the organophosphorus flame retardant, an aryl phosphate compound is suitable. This is because such phosphate compounds are generally excellent in hue. Moreover, since the phosphate compound has a plasticizing effect, it is advantageous in that the molding processability can be improved. As such phosphate compounds, various phosphate compounds known as conventional flame retardants can be used, and more preferably, one or more phosphate compounds represented by the following general formula [9] can be mentioned.

(However, M in the above formula represents a divalent organic group derived from a dihydric phenol, and R ⁹ , R ¹⁰ , R ¹¹ , and R ¹² are each a monovalent organic group derived from a monohydric phenol. E, f, g and h are each independently 0 or 1, m is an integer of 0 to 5, and m is an average value in the case of a mixture of phosphate esters having different degrees of polymerization m. Represents a value between 0 and 5.)

  The phosphate compound of the above formula may be a mixture of compounds having different m numbers, in which case the average m number is preferably 0.5 to 1.5, more preferably 0.8 to 1. 2, More preferably, it is 0.95-1.15, Most preferably, it is the range of 1-1.14.

Preferred specific examples of the dihydric phenol for deriving M in the above formula include hydroquinone, resorcinol, bis (4-hydroxybiphenyl) methane, bisphenol A, dihydroxybiphenyl, dihydroxynaphthalene, bis (4-hydroxyphenyl) sulfone, Examples thereof include a divalent group obtained by removing two hydroxyl groups of a dihydroxy compound selected from the group consisting of bis (4-hydroxyphenyl) ketone and bis (4-hydroxyphenyl) sulfide. Specific examples of R ⁹ , R ¹⁰ , R ¹¹ , and R ¹² include phenol, cresol, xylenol, isopropylphenol, butylphenol, and p-cumyl each independently substituted with one or more halogen atoms. Examples thereof include monovalent groups obtained by removing one hydroxyl group of a monohydroxy compound selected from the group consisting of phenol.

Preferable specific examples of the monohydric phenol for deriving R ⁹ , R ¹⁰ , R ¹¹ , and R ¹² include phenol, cresol, xylenol, isopropylphenol, butylphenol, and p-cumylphenol. Are phenol and 2,6-dimethylphenol.
The monohydric phenol may be substituted with a halogen atom. Specific examples of the phosphate compound having a group derived from the monohydric phenol include tris (2,4,6-tribromophenyl) phosphate and tris. Examples include (2,4-dibromophenyl) phosphate, tris (4-bromophenyl) phosphate, and the like.

On the other hand, specific examples of the phosphate compound not substituted with a halogen atom include monophosphate compounds such as triphenyl phosphate and tri (2,6-xylyl) phosphate, and resorcinol bisdi (2,6-xylyl) phosphate). Preferred are phosphate oligomers mainly composed of phosphate oligomers, phosphate oligomers mainly composed of 4,4-dihydroxydiphenyl bis (diphenyl phosphate), and phosphate oligomers mainly composed of bisphenol A bis (diphenyl phosphate). Indicates that a small amount of other components having different degrees of polymerization may be included, and more preferably, the component of n = 1 in the formula [6] is 80% by weight or more, more preferably 85% by weight or more, and still more preferably Contains over 90% by weight Are shown.).
The compounding amount of the organophosphorus flame retardant is preferably 0.01 to 20 parts by weight, more preferably 2 to 10 parts by weight, and further preferably 2 to 7 parts by weight with respect to 100 parts by weight of the total of component A and component B. It is.

(Iii) Silicone Flame Retardant A silicone compound used as a silicone flame retardant improves flame retardancy by a chemical reaction during combustion. As the compound, various compounds conventionally proposed as a flame retardant for aromatic polycarbonate resin can be used. The silicone compound binds itself during combustion or binds to a component derived from the resin to form a structure, or gives a flame retardant effect to the polycarbonate resin by a reduction reaction during the structure formation. It is considered. Therefore, it is preferable that a group having high activity in such a reaction is contained, and more specifically, a predetermined amount of at least one group selected from an alkoxy group and a hydrogen (ie, Si—H group) is contained. preferable. As a content rate of this group (alkoxy group, Si-H group), the range of 0.1-1.2 mol / 100g is preferable, the range of 0.12-1 mol / 100g is more preferable, 0.15-0. The range of 6 mol / 100 g is more preferable. Such a ratio can be determined by measuring the amount of hydrogen or alcohol generated per unit weight of the silicone compound by the alkali decomposition method. The alkoxy group is preferably an alkoxy group having 1 to 4 carbon atoms, and particularly preferably a methoxy group.

Generally, the structure of a silicone compound is constituted by arbitrarily combining the following four types of siloxane units. That is, M units: (CH ₃ ) ₃ SiO _1/2 , H (CH ₃ ) ₂ SiO _1/2 , H ₂ (CH ₃ ) SiO _1/2 , (CH ₃ ) ₂ (CH ₂ = CH) SiO _{1 / 2} , monofunctional siloxane units such as (CH ₃ ) ₂ (C ₆ H ₅ ) SiO _1/2 , (CH ₃ ) (C ₆ H ₅ ) (CH ₂ ═CH) SiO _1/2 , D unit: _{2 such as} (CH ₃ ) ₂ SiO, H (CH ₃ ) SiO, H ₂ SiO, H (C ₆ H ₅ ) SiO, (CH ₃ ) (CH ₂ ═CH) SiO, (C ₆ H ₅ ) ₂ SiO Functional siloxane unit, T unit: (CH ₃ ) SiO _3/2 , (C ₃ H ₇ ) SiO _3/2 , HSiO _3/2 , (CH ₂ ═CH) SiO _3/2 , (C ₆ H ₅ ) trifunctional siloxane units SiO _3/2, etc., Q unit: 4 represented by SiO ₂ It is a functional siloxane units.

Specifically, the structure of the silicone compound used in the silicone-based flame retardant is represented by the following formulas: D _n , T _p , M _m D _n , M _m T _p , M _m Q _q , M _m D _n T _{p , M m D n Q q,} M m T p Q q, M m D n T p Q q, D n T p, D n Q q, include _{D n} T p _{Q q.} Among these, preferable structures of the silicone compound are M _m D _n , M _m T _p , M _m D _n T _p , and M _m D _n Q _q , and more preferable structures are M _m D _n or M _m D _n. T _p .

Here, the coefficients m, n, p, and q in the above formula are integers of 1 or more that indicate the degree of polymerization of each siloxane unit, and the sum of the coefficients in each formula is the average degree of polymerization of the silicone compound. . This average degree of polymerization is preferably in the range of 3 to 150, more preferably in the range of 3 to 80, still more preferably in the range of 3 to 60, and particularly preferably in the range of 4 to 40. The better the range, the better the flame retardancy. Further, as described later, a silicone compound containing a predetermined amount of an aromatic group is excellent in transparency and hue. As a result, good reflected light can be obtained.
When any of m, n, p, and q is a numerical value of 2 or more, the siloxane unit with the coefficient can be two or more types of siloxane units having different hydrogen atoms or organic residues to be bonded. .

  The silicone compound may be linear or have a branched structure. The organic residue bonded to the silicon atom is preferably an organic residue having 1 to 30 carbon atoms, more preferably 1 to 20 carbon atoms. Specific examples of such an organic residue include alkyl groups such as a methyl group, an ethyl group, a propyl group, a butyl group, a hexyl group, and a decyl group, a cycloalkyl group such as a cyclohexyl group, an aryl group such as a phenyl group, And aralkyl groups such as tolyl groups. More preferably, they are a C1-C8 alkyl group, an alkenyl group, or an aryl group. As the alkyl group, an alkyl group having 1 to 4 carbon atoms such as a methyl group, an ethyl group, and a propyl group is particularly preferable.

  Further, the silicone compound used as the silicone flame retardant preferably contains an aryl group. On the other hand, silane compounds and siloxane compounds as organic surface treatment agents for titanium dioxide pigments are clearly distinguished from silicone-based flame retardants in their preferred embodiments in that it is preferable to contain no aryl group. . A more preferable silicone-based flame retardant is a silicone having a ratio (aromatic group amount) of 10 to 70% by weight (more preferably 15 to 60% by weight) containing an aromatic group represented by the following general formula [10]. A compound.

(In formula [10], B independently represents an OH group and a monovalent organic residue having 1 to 20 carbon atoms. J represents an integer of 0 to 5. Further, in formula [10], j is 2) In these cases, different types of B can be taken.)

The silicone compound used as the silicone-based flame retardant may contain a reactive group in addition to the Si-H group and the alkoxy group. Examples of the reactive group include an amino group, a carboxyl group, an epoxy group, and a vinyl group. Examples thereof include a group, a mercapto group, and a methacryloxy group.
Preferred examples of the silicone compound having a Si—H group include silicone compounds containing at least one of the structural units represented by the following general formulas [11] and [12].

(In the formulas [11] and [12], Z ^{1 to} Z ³ each independently represent a hydrogen atom, a monovalent organic residue having 1 to 20 carbon atoms, or a compound represented by the following general formula [13]. α1 to α3 each independently represents 0 or 1. m1 represents 0 or an integer greater than or equal to 1. Further, in formula [11], when m1 is 2 or more, the repeating units each take a plurality of different repeating units. be able to.)

(In the formula [13], Z ^{4 to} Z ⁸ each independently represent a hydrogen atom or a monovalent organic residue having 1 to 20 carbon atoms. Α4 to α8 each independently represents 0 or 1. m2 represents 0. Alternatively, it represents an integer of 1 or more, and the repeating unit in the case where m2 is 2 or more in the formula [13] can take a plurality of different repeating units.

  Examples of the silicone compound having an alkoxy group in the silicone compound used for the silicone flame retardant include at least one compound selected from compounds represented by the general formula [14] and the general formula [15].

(In the formula [14], β ¹ represents a vinyl group, an alkyl group having 1 to 6 carbon atoms, a cycloalkyl group having 3 to 6 carbon atoms, and an aryl group or aralkyl group having 6 to 12 carbon atoms. Γ ¹ , γ ² , γ ³ , γ ⁴ , γ ⁵ , and γ ⁶ represent an alkyl group and a cycloalkyl group having 1 to ⁶ carbon atoms, and an aryl group and an aralkyl group having 6 to 12 carbon atoms, and at least one group is aryl. And δ ¹ , δ ² , and δ ³ are each an alkoxy group having 1 to 4 carbon atoms.)

(In the formula [15], β ² and β ³ represent a vinyl group, an alkyl group having 1 to 6 carbon atoms, a cycloalkyl group having 3 to 6 carbon atoms, and an aryl group and an aralkyl group having 6 to 12 carbon atoms. γ ⁷ , γ ⁸ , γ ⁹ , γ ¹⁰ , γ ¹¹ , γ ¹² , γ ¹³ and γ ¹⁴ are each an alkyl group having 1 to 6 carbon atoms, a cycloalkyl group having 3 to 6 carbon atoms, An aryl group and an aralkyl group, and at least one group is an aryl group or an aralkyl group, and δ ⁴ , δ ⁵ , δ ⁶ , and δ ⁷ represent an alkoxy group having 1 to 4 carbon atoms.

  The content of the silicone-based flame retardant is preferably 0.01 to 20 parts by weight, more preferably 0.5 to 10 parts by weight, and further preferably 1 to 5 parts by weight with respect to 100 parts by weight of the total of the A component and the B component. Part.

(Iv) Polytetrafluoroethylene (fibrillated PTFE) having fibril-forming ability
The fibrillated PTFE may be fibrillated PTFE alone or a mixed form of fibrillated PTFE, that is, a polytetrafluoroethylene-based mixture composed of fibrillated PTFE particles and an organic polymer. Fibrilized PTFE has an extremely high molecular weight and tends to be bonded to each other by an external action such as shearing force to form a fiber. Its number average molecular weight ranges from 1.5 million to tens of millions. The lower limit is more preferably 3 million. The number average molecular weight is calculated based on the melt viscosity of polytetrafluoroethylene at 380 ° C. as disclosed in JP-A-6-145520. That is, the fibrillated PTFE of the component B has a melt viscosity at 380 ° C. measured by the method described in this publication in the range of 10 ⁷ to 10 ¹³ poise, preferably in the range of 10 ⁸ to 10 ¹² poise. .

  Such PTFE can be used in solid form or in the form of an aqueous dispersion. Such fibrillated PTFE can also be used in the form of a PTFE mixture with other resins in order to improve dispersibility in the resin and to obtain better flame retardancy and mechanical properties. Further, as disclosed in JP-A-6-145520, those having a structure having such a fibrillated PTFE as a core and a low molecular weight polytetrafluoroethylene as a shell are also preferably used.

  Examples of such commercially available fibrillated PTFE include Teflon (registered trademark) 6J from Mitsui DuPont Fluorochemical Co., Ltd., Polyflon MPA FA500, F-201L from Daikin Chemical Industries, Ltd., and the like. Commercially available aqueous dispersions of fibrillated PTFE include: Fluon AD-1, AD-936 manufactured by Asahi IC Fluoropolymers, Fluon D-1, D-2 manufactured by Daikin Industries, Ltd., Mitsui A representative example is Teflon (registered trademark) 30J manufactured by DuPont Fluorochemical Co., Ltd.

  As a mixed form of fibrillated PTFE, (1) a method in which an aqueous dispersion of fibrillated PTFE and an aqueous dispersion or solution of an organic polymer are mixed and co-precipitated to obtain a co-agglomerated mixture (JP-A-60-258263). (2) A method of mixing an aqueous dispersion of fibrillated PTFE and dried organic polymer particles (Japanese Patent Laid-Open No. 4-272957). Described method), (3) A method in which an aqueous dispersion of fibrillated PTFE and an organic polymer particle solution are uniformly mixed, and the respective media are simultaneously removed from the mixture (Japanese Patent Laid-Open Nos. 06-220210, (Method described in Japanese Patent Application Laid-Open No. 08-188653), (4) A method of polymerizing monomers forming an organic polymer in an aqueous dispersion of fibrillated PTFE (Method described in JP-A-9-95583), and (5) an aqueous dispersion of PTFE and an organic polymer dispersion are uniformly mixed, and then a vinyl monomer is further polymerized in the mixed dispersion. Thereafter, those obtained by a method for obtaining a mixture (a method described in JP-A-11-29679, etc.) can be used. Commercial products of these mixed forms of fibrillated PTFE include methabrene represented by Mitsubishi Rayon Co., Ltd.'s "methabrene A3000" (trade name), "methabrene A3700" (trade name), and "methabrene A3800" (trade name). Examples include A series, POLY TS AD001 (trade name) manufactured by PIC, and “BLENDEX B449” (trade name) manufactured by GE Specialty Chemicals.

  The proportion of fibrillated PTFE in the mixed form is preferably 1% by weight to 95% by weight, more preferably 10% by weight to 90% by weight, and more preferably 20% by weight in 100% by weight of the mixture. Most preferred is from 80% to 80% by weight. If it is less than 1% by weight, the ratio of the organic polymer portion in the mixed form in the flame-retardant polycarbonate resin of the present invention tends to increase, so the transparency tends to decrease and the flame-retardant improving effect is also exhibited. It becomes difficult. Above 95% by weight, it becomes difficult to achieve a high level surface appearance. On the other hand, when it exceeds 90% by weight, the difference in performance from PTFE that is not in a mixed form is reduced, and it is advantageous in terms of cost to use fibrillated PTFE that is not in a mixed form.

When the ratio of fibrillated PTFE in the mixed form is within such a range, good dispersibility of the fibrillated PTFE can be achieved.
The content of fibrillated PTFE is preferably 0.1 to 0.2 parts by weight, more preferably 0.1 to 0.19 parts by weight, based on 100 parts by weight of the total of component A and component B. More preferably, the content is 0.1 to 0.18 parts by weight. In addition, the weight part shown here shows the weight of the whole mixture, when polytetrafluoroethylene is a mixed form (mixture).

(Reinforcing filler)
The reinforced polycarbonate resin composition of the present invention contains a fibrous reinforcing filler, but contains at least one reinforcing filler selected from a plate-like reinforcing material and a granular reinforcing material in addition to the fibrous reinforcing filler. May be.

Examples of the plate-like reinforcing material include talc, mica, clay, montmon lilonite, smectite, kaolin, calcium carbonate, glass flake, carbon flake, metal flake, metal-coated glass flake, graphite and the like. The plate-like reinforcing material is suitable for a precision member requiring little dimensional stability because the reinforcing material itself has little anisotropy. The average particle size of the plate-like reinforcing material is preferably in the range of 0.1 to 300 μm, particularly preferably in the range of 0.1 to 200 μm. The average particle size refers to an average particle size (D50 (median diameter of particle size distribution)) measured by a laser diffraction / scattering method. For this measurement, for example, a laser diffraction / scattering particle size distribution measuring apparatus manufactured by Horiba, Ltd. can be used. If the average particle size of the plate-like reinforcing material exceeds 300 μm, clogging may occur in the gate part or the nozzle part of the hot runner, which leads to a decrease in production efficiency in a highly automated recent molding site. In particular, in recent years, there is a tendency to reduce the gate diameter and nozzle diameter in order to improve the molding cycle and the appearance of the molded product, and it is important to solve the clogging problem at a higher level. When the average particle size of the plate-like reinforcing material is less than 0.1 μm, the effect of improving the rigidity and dimensional stability of the plate-like reinforcing material is reduced.
Examples of the particulate reinforcing material include glass beads, glass balloons, carbon beads, ceramic particles, ceramic balloons, aramid particles, and silica.

  The plate-like reinforcing material may be subjected to a focusing treatment with an olefin resin, a styrene resin, an acrylic resin, a polyester resin, an epoxy resin, a urethane resin, or the like as long as the effect of the present invention is not impaired. It may be surface-treated with various surface treatment agents such as coupling agents, higher fatty acid esters, and waxes. Moreover, you may use in the granulated form, and as such a granulation method, there are a case where a binder is used and a case where it is not substantially used, but a method using no binder is more preferable. As a granulation method when a binder is not used, a deaeration compression method (for example, a roller compression with a briquetting machine while deaeration in a vacuum state), a rolling granulation method or an agglomeration granulation method Etc. Further, as described above, the reinforcing filler used in the present invention includes those in which a different material is surface-coated. Preferred examples of such dissimilar materials include metals and metal oxides. Examples of the metal include silver, copper, nickel, and aluminum. Examples of the metal oxide include titanium oxide, cerium oxide, zirconium oxide, iron oxide, aluminum oxide, and silicon oxide. There are no particular limitations on the method of surface coating of such different materials, for example, various known plating methods (for example, electrolytic plating, electroless plating, hot dipping, etc.), vacuum deposition methods, ion plating methods, CVD methods (For example, thermal CVD, MOCVD, plasma CVD, etc.), PVD method, sputtering method, etc. can be mentioned.

  The content of the reinforcing filler other than the component C used in the present invention is preferably 1 to 200 parts by weight, more preferably 1 to 150 parts by weight, and more preferably 10 to 150 parts by weight with respect to 100 parts by weight of the total of the component A and the component B. Is more preferable. When the content of such a reinforcing material is less than 1 part by weight, the effect of improving rigidity and dimensional stability is reduced, and when it exceeds 200 parts by weight, molding processability may be deteriorated due to a decrease in fluidity.

(Preparation method)
There is no restriction | limiting in particular in the method to manufacture the reinforced polycarbonate resin composition of this invention, A well-known method can be used. For example, a method of mixing each component in a solution state and evaporating the solvent or precipitating in the solvent can be mentioned. From an industrial point of view, a method of kneading each component in a molten state is preferable. For melt kneading, generally used kneading apparatuses such as a single or twin screw extruder and various kneaders can be used. A biaxial high kneader is particularly preferable. In the melt-kneading, the cylinder set temperature of the kneading apparatus is preferably in the range of 200 to 360 ° C, more preferably 250 to 340 ° C.

At the time of kneading, each component may be mixed uniformly in advance with a device such as a tumbler or a Henschel mixer, or if necessary, a method of omitting the mixing and separately supplying each of the components separately to the kneading device is also used. be able to.
It is also possible to obtain a reinforced polycarbonate resin composition by melting and kneading an aromatic polycarbonate resin and a liquid crystal polyester resin in advance to obtain a mixture, and then melt-kneading this and a phosphorus stabilizer.

  Further, a kneaded product (component E) prepared by melting and kneading an aromatic polycarbonate resin and a liquid crystal polyester resin is blended with an aromatic polycarbonate resin and / or a liquid crystal polyester resin, a fibrous reinforcing filler, and a phosphorus stabilizer, A reinforced polycarbonate resin composition can also be obtained by melt-kneading.

In this case, the weight ratio of the A component to the B component in the E component is preferably 1/99 to 99/1, more preferably 10/90 to 90/10, still more preferably 20/80 to 80/20, 50 / 50 to 80/20 is most preferable. Also, polycarbonate resin and liquid crystal polyester resin are charged from the first inlet of the kneader, and fibrous reinforcing filler, phosphorus stabilizer and aromatic polycarbonate resin and / or liquid crystal polyester resin are charged from the second inlet. The polycarbonate resin composition can be obtained by one kneading.
The resin composition is molded by injection molding, extrusion molding, and other various molding methods, but does not go through a kneading process in advance, dry blended during injection molding or extrusion molding, and kneaded during a melt processing operation, The resin composition of the present invention can be directly obtained as a molded product.

  The molded article comprising the reinforced polycarbonate resin composition of the present invention preferably has an average fibril diameter of 0.01 to 3 μm, preferably 0.01 to 2 μm, after the surface is treated with hydrazine. Is more preferable, and it is still more preferable that it is 0.01-1 micrometer. If the average fibril diameter of the component B is less than 0.01 μm, the rigidity is difficult to develop, and if it exceeds 3 μm, the strength is not obtained. The average fibril diameter of the above B component is the average of the remaining B component after immersing the molded product in hydrazine monohydrate for 30 seconds and washing with methanol, and then observing the surface of the molded product with a scanning electron microscope. It was calculated by measuring the fibril diameter.

  The reinforced polycarbonate resin composition of the present invention is excellent not only in rigidity and molding processability but also in strength, such as various electronic / electric equipment, OA equipment, vehicle parts, machine parts, other agricultural materials, transport containers, playground equipment, miscellaneous goods, etc. It is useful for various applications, especially for thin precision parts, and the industrial effects it produces are exceptional.

Molded product body (360 × 250 × 1.0) simulating the housing of a notebook computer in which the pellets obtained in the examples and comparative examples were molded by an injection molding machine (ULTRA220-NIVA manufactured by Sumitomo Heavy Industries, Ltd.) mm)).

  The form for carrying out the present invention is a summary of the preferred ranges of the above-mentioned requirements. For example, typical examples are described in the following examples. Of course, the present invention is not limited to these forms.

Hereinafter, the present invention will be described in detail by way of examples. However, the present invention is not limited to these.
In addition, the measurement of the various characteristics in an Example was based on the following method.

1. Physical property measuring method 1) Alkali (earth) metal content in component B Liquid crystalline polyester resin is thermally decomposed with sulfuric acid and nitric acid, then the volume is adjusted with ultrapure water to obtain a test solution, and inductively coupled plasma emission spectroscopy (ICP-) By AES), elemental analysis of alkali metal and / or alkaline earth metal in the test solution was performed. (Apparatus: SPS5100 manufactured by SII Nano Technology)

2) Transesterification rate Pellets obtained by the following method were dissolved in methylene chloride, and the filtrate obtained by filtering the obtained solution using filter paper (retained particle diameter: 7 μm) was obtained at 120 ° C. Let dry for hours. The filtrate was dissolved in deuterated chloroform, ¹ H-NMR was measured using a magnetic resonance apparatus, and a peak of 7.8 to 8.1 ppm derived from a co-reacted product of polycarbonate resin and liquid crystal polyester resin, and polycarbonate resin The transesterification rate was calculated from the integral ratio calculated from the peak of 7.1 to 7.3 ppm derived from the following formula.
Transesterification rate (%) = 100 × (integral ratio calculated from peak derived from co-reactant) / (integral ratio calculated from peak derived from co-reactant + integral ratio calculated from peak derived from polycarbonate resin)

3) Rigidity The pellet obtained by the following method was dried with a hot air dryer at 120 ° C. for 5 hours, and then the cylinder temperature was 310 ° C. and the mold using an injection molding machine (Sumitomo Heavy Industries, Ltd. SG-150U). A bending test piece (thickness 1.6 mm) was prepared at a temperature of 90 ° C., and the flexural modulus, flexural strength and flexural strain were measured in accordance with ISO178.

4) Fluidity After pellets obtained by the following method were dried by a hot air dryer at 120 ° C. for 5 hours, an Archimedean spiral length with a channel thickness of 1 mm and a channel width of 8 mm was formed into an injection molding machine (Sumitomo Heavy Industries, Ltd. ( It was measured from the flow length when injection molding was performed at a cylinder temperature of 300 ° C., a mold temperature of 80 ° C., and an injection pressure of 118 MPa by SG-150U).

5) Moldability After pellets obtained by the following method were dried with a hot air dryer at 120 ° C for 5 hours, a cylinder temperature of 310 ° C was used using an injection molding machine (Sumitomo Heavy Industries, Ltd. SG-150U). Bending test pieces (thickness 1.6 mm) were prepared at a mold temperature of 90 ° C., and the appearance was evaluated according to the following criteria.
○: No short shot, sink, or burr on molded product ×: Short shot, sink, or burr on molded product

6) Melt heat stability After drying the pellet obtained by the following method at 120 degreeC with a hot air dryer for 5 hours, cylinder temperature 330 degreeC using an injection molding machine (Sumitomo Heavy Industries, Ltd. SG-150U). After being retained for 20 minutes, a bending test piece (wall thickness: 1.6 mm) was prepared at a mold temperature of 90 ° C., and the appearance was evaluated according to the following criteria.
○: No short shot, silver, sink mark on molded product ×: Short shot, silver, sink mark on molded product

2. Evaluation method of molded product 1) Bending flexibility After pellets obtained by the following method are dried with a hot air dryer at 120 ° C. for 5 hours, an injection molding machine (ULTRA220-NIVA manufactured by Sumitomo Heavy Industries, Ltd.) is used. 1 was molded at a cylinder temperature of 310 ° C. and a mold temperature of 90 ° C.
The obtained notebook personal computer exterior part simulated molded product was allowed to stand on a flat surface, and after fixing one side of the molded product, the cracking property when the portion opposite to the fixed side was lifted by 150 mm was evaluated. The evaluation method was performed according to the following criteria.
○: No crack or crack occurrence ×: Crack or crack occurrence

2) B component fibril diameter on the surface of the molded article The obtained notebook PC exterior part simulated molded article was immersed in hydrazine monohydrate for 30 seconds and washed with methanol, and then the surface of the molded article was observed with a scanning electron microscope. It was calculated by measuring the average fibril diameter of the remaining B component.

3. Preparation of transesterification product (component E) of aromatic polycarbonate resin (component A) and liquid crystalline polyester resin (component B) Aromatic polycarbonate resin powder (component A), liquid crystalline polyester resin (component B), and phosphorus stabilizer (D component) was blended in the respective blending amounts shown in Table 1, mixed with a blender, and then vented twin-screw extruder (manufactured by Nippon Steel Works, Ltd .: TEX30α (completely meshing, rotating in the same direction, double thread) The pellets (E-1 to E-10) were obtained by melt kneading using a screw)). The extrusion conditions were a discharge rate of 20 kg / h, a screw rotation speed of 150 rpm, a vent vacuum of 3 kPa, and an extrusion temperature of 280 ° C. from the first supply port to the die part. Table 1 shows the transesterification rate of the obtained pellets.

In addition, the content of each component indicated by symbols in Table 1 is as follows. Hereinafter, “part” means “part by weight” and “%” means “% by weight” unless otherwise specified.
(Component A)
PC-1: Polycarbonate composed of 4,4′-dihydroxy-2,2′-diphenylpropane (PC-1 production method)
A reactor equipped with a thermometer, a stirrer, and a reflux condenser was charged with 2340 parts of ion-exchanged water, 947 parts of a 25% aqueous sodium hydroxide solution and 0.7 parts of hydrosulfite, and 2,2-bis (4-hydroxyphenyl) under stirring. ) After dissolving 710 parts of propane (hereinafter sometimes referred to as “bisphenol A”) (bisphenol A solution), 2299 parts of methylene chloride and 112 parts of 48.5% aqueous sodium hydroxide solution were added, and the temperature was 15-25 ° C. The phosgenation reaction was performed by blowing 354 parts of phosgene over about 90 minutes.
After the completion of phosgenation, 148 parts of 11% strength p-tert-butylphenol in methylene chloride and 88 parts of 48.5% aqueous sodium hydroxide solution were added, stirring was stopped, and the mixture was allowed to stand for 10 minutes, followed by stirring. After 5 minutes of emulsification, the mixture was processed with a homomixer (Special Machine Industries Co., Ltd.) at a rotation speed of 1200 rpm and a bath frequency of 35 times to obtain a highly emulsified dope. The highly emulsified dope was reacted in a polymerization tank (with a stirrer) for 3 hours at 35 ° C. under non-stirring conditions to complete the polymerization. After completion of the reaction, 5728 parts of methylene chloride was added for dilution, the methylene chloride phase was separated from the reaction mixture, 5000 parts of ion-exchanged water was added to the separated methylene chloride phase and mixed with stirring, and the stirring was stopped. The phase and the organic phase were separated. Next, water washing was repeated until the conductivity of the aqueous phase was almost the same as that of ion-exchanged water to obtain a purified polycarbonate resin solution. Next, this resin solution was put into a kneader filled with warm water, and methylene chloride was evaporated while stirring to obtain a polycarbonate resin granule. After dehydration, it was dried at 120 ° C. for 12 hours using a hot air circulating dryer. This polycarbonate had a viscosity average molecular weight of 19,700.

PC-2: A polycarbonate-polydimethylsiloxane copolymer comprising 4,4′-dihydroxy-2,2′-diphenylpropane and a bisphenol compound having a polydimethylsiloxane structure represented by the following formula [16].
(Method for producing PC-2)
In the method for producing PC-1, after the completion of phosgenation, 148 parts of an 11% strength p-tert-butylphenol methylene chloride solution and 88 parts of a 48.5% aqueous sodium hydroxide solution were added, and the following formula [16 ] A polydiorganosiloxane compound (X-22-1821 manufactured by Shin-Etsu Chemical Co., Ltd.) having the following structure represented by the following formula: It was made into the highly emulsified state by stirring at 8000 rpm for 2 minutes, and then kept at 35 ± 1 ° C. for 2 hours in a stationary state without stirring. A granule of a polycarbonate-polydimethylsiloxane copolymer was obtained. This polycarbonate had a viscosity average molecular weight of 19,500.

(B component)
LCP-1: Liquid crystal polyester resin having an alkali metal content of 35 ppm (production method of LCP-1)
Reaction with 5400 parts by weight of p-acetoxybenzoic acid, 4320 parts by weight of 2,6-naphthalenedicarboxylic acid, and 0.01% by weight of potassium acetate based on the total charge, each equipped with a stirrer, a nitrogen introduction tube and a distillation tube The mixture was charged into a vessel and the mixture was heated to 260 ° C. for 1 hour under a nitrogen stream. While distilling acetic acid from the reactor, it was heated to 260-300 ° C. over 2 hours, further heated at 300 ° C. for 2 hours, and acetic acid was distilled off under reduced pressure (2 mmHg). Next, nitrogen was introduced and cooled to room temperature to obtain a light yellow milky white liquid crystal polyester resin. The amount of alkali metal contained in the liquid crystalline polyester resin was 35 ppm.

LCP-2: Liquid crystal polyester resin having an alkali metal content of 140 ppm (method for producing LCP-2)
5400 parts by weight of p-acetoxybenzoic acid, 1080 parts by weight of 2,6-naphthalenedicarboxylic acid, 1080 parts by weight of 2,7-naphthalenedicarboxylic acid, 2070 parts by weight of 4,4′-diacetoxybiphenyl, and 0. Each of 05 wt% potassium acetate was charged into a reactor equipped with a stirrer, a nitrogen inlet tube and a distillation tube, and the mixture was heated to 260 ° C. for 1 hour under a nitrogen stream. While distilling acetic acid from the reactor, it was heated to 260-300 ° C. over 2 hours, further heated at 300 ° C. for 2 hours, and acetic acid was distilled off under reduced pressure (2 mmHg). Next, nitrogen was introduced and cooled to room temperature to obtain a light yellow milky white liquid crystal polyester resin. The amount of alkali metal contained in the liquid crystalline polyester resin was 140 ppm.

LCP-3: Liquid crystal polyester resin having an alkali metal content of 3 ppm (production method of LCP-3)
5400 parts by weight of p-acetoxybenzoic acid, 1080 parts by weight of 2,6-naphthalenedicarboxylic acid, 1080 parts by weight of 2,7-naphthalenedicarboxylic acid, 2070 parts by weight of 4,4′-diacetoxybiphenyl, and 0. 008% by weight of potassium acetate was charged into a reactor equipped with a stirrer, a nitrogen inlet tube and a distillation tube, respectively, and the mixture was heated to 260 ° C. for 1 hour under a nitrogen stream. While acetic acid was distilled from the reactor, the mixture was heated to 260 to 300 ° C. over 3 hours, further heated at 300 ° C. for 6 hours, and acetic acid was distilled off under reduced pressure (2 mmHg). Next, nitrogen was introduced and cooled to room temperature to obtain a light yellow liquid crystal polyester resin. The amount of alkali metal contained in this liquid crystalline polyester resin was 3 ppm.

LCP-4: Liquid crystal polyester resin having an alkali metal content of 350 ppm (production method of LCP-4)
5400 parts by weight of p-acetoxybenzoic acid, 1080 parts by weight of 2,6-naphthalenedicarboxylic acid, 1080 parts by weight of 2,7-naphthalenedicarboxylic acid, 2070 parts by weight of 4,4′-diacetoxybiphenyl, and 0. 13% by weight of potassium acetate was charged into a reactor equipped with a stirrer, a nitrogen inlet tube and a distillation tube, respectively, and the mixture was heated to 260 ° C. for 1 hour under a nitrogen stream. While distilling acetic acid from the reactor, it was heated to 260-300 ° C. over 2 hours, further heated at 300 ° C. for 2 hours, and acetic acid was distilled off under reduced pressure (2 mmHg). Next, nitrogen was introduced and cooled to room temperature to obtain a yellow liquid crystal polyester resin. The amount of alkali metal contained in the liquid crystalline polyester resin was 350 ppm.

(C component)
GF-1: flat cross-section chopped glass fiber (manufactured by Nitto Boseki Co., Ltd .: CSG 3PA-830 (trade name), major axis 28 μm, minor diameter 7 μm, cut length 3 mm, epoxy sizing agent)
GF-2: Circular cross-section glass fiber (manufactured by Nitto Boseki Co., Ltd .: 3PE937 (trade name), fiber diameter: 13 μm, cut length: 3 mm, aminosilane-treated surface treatment and epoxy / urethane sizing agent)
CF-1: Best Fight HTA-C6-U (trade name) (carbon fiber diameter 7.5 μm, cut length 6 mm, manufactured by Toho Tenax Co., Ltd.)
(D component)
D-1: ADK STAB PEP-8 (trade name) (distearyl pentaerythritol diphosphite manufactured by Asahi Denka Kogyo Co., Ltd.)
D-2: ADK STAB PEP-24G (trade name) (Bis (2,4-di-tert-butylphenyl) pentaerythritol diphosphite manufactured by Asahi Denka Kogyo Co., Ltd.)
(Other ingredients)
TMP: TMP (trade name) (trimethyl phosphate, manufactured by Daihachi Chemical Industry Co., Ltd.)

[Examples 1-9 and Comparative Examples 1-10]
After blending the aromatic polycarbonate resin obtained above, liquid crystal polyester resin, fibrous reinforcing filler, phosphorus compound and the pellets obtained by the above method in each blending amount described in Table 2, and mixing in a blender, Pellets were obtained by melt-kneading using a vent type twin screw extruder (manufactured by Nippon Steel Works, Ltd .: TEX30α (completely meshing, rotating in the same direction, two-thread screw)). The phosphorus compound to be used was prepared in advance as a pre-mixture with a polycarbonate resin with a concentration of 10 to 100 times the blending amount as a guide, and then the whole was mixed by a blender. The extrusion conditions were a discharge rate of 20 kg / h, a screw rotation speed of 150 rpm, a vent vacuum of 3 kPa, and an extrusion temperature of 280 ° C. from the first supply port to the die part. The obtained pellets were dried with a hot air circulation dryer at 80 ° C. for 6 hours, and then a test piece for evaluation was molded using an injection molding machine. The evaluation results are shown in Table 2. In Comparative Examples 5, 6 and 9, the measured value of the transesterification rate was not constant due to the poor thermal stability of the resin composition, so that the measurement was impossible.

[Example 10]
The bending flexibility and the average fibril diameter of the B component of the laptop computer exterior component simulated molded article made of the pellets obtained in Example 1 were measured. The results are shown in Table 3.

[Comparative Example 11]
The bending flexibility and the average fibril diameter of the B component of the laptop computer exterior component simulated molded article made of the pellets obtained in Comparative Example 7 were measured. The results are shown in Table 3.

1. Molded product body that mimics the laptop housing (360 x 250 x 1.0 (mm))
2. 2. Matte surface part Mirror surface

Claims (8)

  (C) Fibrous reinforcing filler with respect to 100 parts by weight of resin component consisting of 98 to 60% by weight of aromatic polycarbonate resin (component A) and (B) 2 to 40% by weight of liquid crystal polyester resin (component B) In the reinforced polycarbonate resin composition comprising (C component) 10 to 150 parts by weight and (D) phosphorus stabilizer (D component) 0.001 to 2 parts by weight, alkali metal and / or alkali contained in component B A reinforced polycarbonate resin composition, wherein the earth metal content is in the range of 5 to 300 ppm, and a part of the A component and B component in the obtained resin composition is transesterified.   The reinforced polycarbonate resin composition according to claim 1, wherein the component B is a liquid crystal polyester resin polymerized using p-hydroxybenzoic acid and 6-hydroxy-2-naphthoic acid as raw materials.   C component is glass fiber, The reinforced polycarbonate resin composition of Claim 1 or 2 characterized by the above-mentioned.   The C component is a glass fiber containing a flat cross-section glass fiber having an average value of the ratio of the major axis to the minor axis (major axis / minor axis) of 3.2 to 8 in the fiber cross section. Reinforced polycarbonate resin composition.   C component is carbon fiber, The reinforced polycarbonate resin composition of Claim 1 or 2 characterized by the above-mentioned. The reinforced polycarbonate resin composition according to any one of claims 1 to 5, wherein the D component is a pentaerythritol diphosphite compound represented by the following general formula [1].
[Wherein A ¹ and A ² are each independently a hydrogen atom, an alkyl group having 1 to 20 carbon atoms, an aryl group or an alkylaryl group having 6 to 20 carbon atoms, an aralkyl group having 7 to 30 carbon atoms, or a carbon number. A group selected from the group consisting of 4 to 20 cycloalkyl groups and 2- (4-oxyphenyl) propyl-substituted aryl groups having 15 to 25 carbon atoms. In addition, the cycloalkyl group and the aryl group may be substituted with an alkyl group. ] (E) A mixture of an A component and a B component prepared by reacting an aromatic polycarbonate resin (A component) and a liquid crystal polyester resin (B component) with an extruder (E component), and (A) a polycarbonate resin (A component) ) And / or (B) liquid crystal polyester resin (component B), (C) fibrous reinforcing filler (component C) and (D) phosphorus stabilizer (component D) are prepared by melt-kneading again. The manufacturing method of the reinforced polycarbonate resin composition in any one of Claims 1-6 characterized by the above-mentioned. After the surface of the molded product is treated with hydrazine, the average fibril diameter of the remaining B component is 0.01 to 3 µm, and consists of the reinforced polycarbonate resin composition according to any one of claims 1 to 6. Molding.