JPH06287430A - Polycarbonate resin composition - Google Patents

Abstract

PURPOSE:To obtain the subject composition excellent in flame retardance, mechanical strength, etc., useful for flame retardant parts of construction materials, OA equipments, etc., and comprising a rubbery elastomer and a polycarnonate-polyorganosiloxane copolymer having a specific main chain. CONSTITUTION:The objective composition comprises (A) 1-99(wt.)% polycarbonate-polyorganosiloxane having a main chain consisting of (i) a repeating unit of the formula I (R1 and R2 are H or 1-4C alkyl), (ii) a repeating unit of the formula II (R3 and R4 are H or 1-4C alkyl; X1-X4 are halogen) and (iii) a structural unit of the formula III (R5-R8 are H, 1-6C alkyl or phenyl; R9 and R10 are an organic residue containing an aliphatic or an aromatic group; A is a single bond of O or NH; k is 1-500) and a terminal polyhalogenophenoxy group of the formula IV (X5 is halogen; m is 1-5) and 99-1% rubbery elastomer.

Description

Detailed Description of the Invention

[0001]

FIELD OF THE INVENTION The present invention relates to a polycarbonate resin composition. More specifically, flame retardancy, mechanical strength,
The present invention relates to a polycarbonate resin composition having excellent fluidity and releasability.

[0002]

2. Description of the Related Art Conventionally, various flame-retardant halogen-containing copolycarbonates have been proposed. For example, Japanese Patent Publication No. 46-40715 and Japanese Patent Publication No. 47-24660.
Japanese Patent Publication [Tetrabromobisphenol A (TBA) and Bisphenol A (BPA) Copolymer], JP-A-51
-123294 (copolymer of tetrabromobisphenol sulfone (TBS) and BPA), JP-A-51
No. 136796 [Copolymer of statistical mixture of halogenated bisphenol and BPA], JP-A-52-14
No. 0597, JP-A-54-50065 [Copolymer of thiodiphenol (TDP) and BPA, tetrabromobisphenol A (TBA) and bisphenol A]
Blend with (BPA) Copolymer], JP-A-56-
No. 99226 [Tetrabromothiodiphenol (T
BTDP) and BPA copolymer] and the like are known. These copolymers are obtained by copolymerizing halogenated bisphenols in which the benzene nucleus of bisphenols is substituted with halogen in order to contain the amount of halogen required to impart flame retardancy. However, both of them have a problem that these halogenated bisphenols must be used in a relatively large amount, and accordingly, the mechanical strength (particularly impact resistance strength) of the polycarbonate must be sacrificed. Other halogen-containing polycarbonates are also known in Japanese Examined Patent Publication No. 46-40715 [using halogenated phenols as terminal terminators]. However, also in this case, it is not possible to impart both flame retardancy and mechanical strength. As a method of improving the above-mentioned drawbacks, a method of copolymerizing BPA and a halogenated bisphenol by using polyhalogenophenol as an end terminating agent [eg, JP-A-64-79]
No. 227, Japanese Patent Application Laid-Open No. 64-79228, Japanese Patent Application Laid-Open No. 3-200833, etc.] are known. With this method, flame retardancy and impact resistance can be imparted at the same time, but as a result of further research, the present inventors succeeded in exhibiting excellent mechanical strength and fluidity.

[0003]

[Means for Solving the Problem] That is, a polycarbonate-polyorganosiloxane copolymer obtained by copolymerizing bisphenols, halogenated bisphenols, and polyorganosiloxane, using polyhalogenophenol as a terminal stopper, It has been found that a polycarbonate resin composition prepared by blending a rubber-like elastic body has desired properties. The present invention has been completed based on such findings.

That is, in the present invention, (A) the main chain is
(A) General formula (I)

[0005]

[Chemical 5]

[In the formula, R ¹ and R ² each represent a hydrogen atom or an alkyl group having 1 to 4 carbon atoms, and may be the same or different. ] The repeating unit I represented by the formula (b) general formula (II)

[0007]

[Chemical 6]

[In the formula, R ³ and R ⁴ each represent a hydrogen atom or an alkyl group having 1 to 4 carbon atoms, and may be the same or different. Also, X ¹ ~
X ⁴ each represents a halogen atom. ] The repeating unit II and (c) the general formula (III)

[0009]

[Chemical 7]

[Wherein R^Five~ R⁸Is the hydrogen source
Child, an alkyl group having 1 to 6 carbon atoms or a phenyl group
But they may be the same or different
Yes. Also, R ⁹And R^TenAre respectively aliphatic or aromatic
Represents an organic residue containing a group, A is -O-, -NH- or
Indicates a single bond. k is an integer of 1 to 500. ]]
Of the general formula (IV)

[0011]

[Chemical 8]

[In the formula, X ⁵ represents a halogen atom, and m is an integer of 1 to 5. When m is plural, plural X
Each ⁵ may be the same or different. ] The end group IV of the polyhalogenophenoxy group represented by
1 to 99% by weight of a polycarbonate-polyorganosiloxane copolymer and (B) a rubber-like elastic material 99 to 1.
The present invention provides a polycarbonate resin composition, which is characterized in that it is composed by weight.

The polycarbonate resin composition of the present invention is prepared.
Component (A) Polycarbonate-Polyorgano
Roxane copolymer (hereinafter abbreviated as PC-PDMS copolymer)
You ) Is represented by the general formula (I) in which the main chain is the component (a).
Represented by the general formula (II), which is the repeating unit I and the component (b)
Repeating unit II and a general formula (III) which is the component (c)
In addition to having a structural unit III represented by the general formula (IV)
The end group IV of the polyhalogenophenoxy group represented by
It is something. Here, the repetition represented by the general formula (I)
R in unit I¹And R²Are hydrogen atom or charcoal, respectively
Alkyl groups of prime number 1 to 4 (methyl group, ethyl group, propyl group
Group, butyl group), even if they are the same
It may be one. Further, the repeating represented by the general formula (II)
X in return unit II¹~ X^FourAre bromine atom and chlorine, respectively
Indicates a halogen atom such as atom, fluorine atom, iodine atom, etc.
You This X¹~ X ^FourAre different even if they are the same
May be, but is usually the same
There are many. And in the repeating unit II represented by the general formula (II)
R³And R^FourFor the above R¹And R²alike
Each is a hydrogen atom or an alkyl group having 1 to 4 carbon atoms (
(Cyl group, ethyl group, propyl group, butyl group)
They may be the same or different. Change
In the structural unit III represented by the general formula (III)^Five~ R
⁸Are a hydrogen atom and an alkyl group having 1 to 6 carbon atoms, respectively.
Or a phenyl group. This R^Five~ R⁸Are the same
It may be the same or different. Also, R⁹Over
And R^TenIs an organic residue containing aliphatic or aromatic, respectively
And A represents -O-, -NH- or a single bond. k
Is an integer of 1 to 500, preferably 5 to 400. This
PC-PDMS copolymers of
The terminal group IV represented by the general formula (IV) at the terminal position, that is, poly
A halogenophenoxy group is attached. This general formula (IV)
X in the terminal group IV represented by^FiveIs the above X¹~ X^Fourin the case of
Like bromine atom, chlorine atom, fluorine atom,
Indicates a halogen atom such as iodine atom, m is an integer of 1 to 5
Is. When m is plural, plural X^FiveAre the same
It may be different or different. The above general formula
X in the repeating unit II represented by (II)¹~ X^FourAnd the general formula (I
X in the terminal group IV represented by V)^FiveIs the same
It may be different. This PC-PDMS copolymerization
The body is composed of the above repeating unit I, repeating unit II and structural unit II.
Has I and ends at the end position (preferably both end positions)
It has a constitution in which the polyhalogenophenoxy group of the end group IV is bonded.
These repeating units I, repeating units II and structural units II
Random copolymer, block copolymer, alternating copolymer of I
There are various things such as the body.

In this PC-PDMS copolymer,
The proportion of the repeating unit II represented by the general formula (II), which is the component (b), is 1 to 10 mol%, preferably 2 to 8 mol% with respect to the total amount of the repeating unit I and the repeating unit II. is there.
If the proportion of the repeating unit II is less than 1 mol%, the flame retardancy-improving effect is not observed. Further, if it exceeds 10 mol%, mechanical strength such as impact resistance decreases. In addition, the structural unit represented by the general formula (III) which is the component (c)
The proportion of III is 0.01 to 10% by weight, preferably 0.02 to 8% by weight, based on the total amount of repeating unit I, repeating unit II and structural unit III. If the proportion of the structural unit III is less than 0.01% by weight, the mechanical strength such as flame retardancy and impact resistance will decrease. Further, when it exceeds 10% by weight,
It is not preferable because the heat resistance is lowered. And its viscosity average molecular weight is from 1,000,000 to 5,000,000, preferably 12,000.
~ 40,000. When the viscosity average molecular weight is less than 10,000, the mechanical strength such as impact resistance decreases. Also, 5
When it exceeds 0000, fluidity is lowered and moldability is deteriorated, which is not preferable. The content of halogen atoms in this PC-PDMS copolymer is 4% by weight or more, preferably
It is 4.5% by weight or more. If the content of halogen atoms is less than 4% by weight, the flame retardancy is lowered, which is not preferable.

Examples of an efficient and preferable method for producing such a PC-PDMS copolymer include, but are not limited to, the following methods. First, in the presence of a known acid acceptor and molecular weight modifier in a solvent such as methylene chloride, if necessary, the following general formula (V)

[0016]

[Chemical 9]

[In the formula, R ¹ and R ² are the same as defined above. ] The bisphenols represented by and phosgene are reacted with each other to cause substantially all of the phosgene in the reaction system to react to produce a polycarbonate oligomer (hereinafter abbreviated as PC oligomer). This PC oligomer has a repeating unit I represented by the general formula (I) which is formed by the reaction of bisphenols and phosgene in the polycondensation reaction. That is, the PC oligomer having the repeating unit I represented by the general formula (I) is reacted with 100 bisphenols at a molar ratio of phosgene 110 to 150. Usually, in this reaction, bisphenols are added in an alkaline aqueous solution, and the mixture is stirred with a solvent such as methylene chloride, chlorobenzene, chloroform, carbon tetrachloride, etc. and, if necessary, a catalyst such as triethylamine or trimethylbenzylammonium chloride at a predetermined ratio. Then blow phosgene into it for 1 to 3 hours at a reaction temperature of 3
It can be produced by proceeding the interfacial polycondensation reaction at 0 to 70 ° C. At this time, the reaction system generates heat, so it is preferable to cool with water or ice. Moreover, since the reaction system shifts to the acidic side as the reaction progresses, it is preferable to maintain the pH at 10 or more by adding an alkaline compound while measuring with a pH meter. P obtained in this way
The C oligomer has an average molecular weight of 2,000 or less and is 1 to 1
It is a zero-mer.

Then, after reacting substantially all of the phosgene in the reaction system, the PC oligomer having the repeating unit I represented by the general formula (I) is added to the following general formula (VI).

[0019]

[Chemical 10]

[In the formula, R ³ , R ⁴ and X ^{1 to} X ⁴ are the same as defined above. ] An alkaline aqueous solution of tetrahalogenobisphenols represented by the following general formula (VII)

[0021]

[Chemical 11]

[In the formula, X ⁵ and m are the same as defined above. ] An alkaline aqueous solution of polyhalogenophenol represented by the following formula and a catalyst such as triethylamine or trimethylbenzylammonium chloride are mixed and stirred at a predetermined ratio to perform polymerization, and a polycarbonate copolymer oligomer (hereinafter abbreviated as PC copolymer oligomer). To manufacture.
This PC copolymer oligomer is based on 100 bisphenol units in the PC oligomer, tetrahalogenobisphenols 1.2 to 14 and polyhalogenophenol 0.3.
Obtained by reacting at a molar ratio of ˜6.0. The PC copolymer oligomer obtained has the repeating unit II represented by the general formula (II) and the repeating unit I represented by the general formula (I), which are formed by the reaction with tetrahalogenobisphenols in the above reaction. Have. Here, as the bisphenols represented by the general formula (V),
For example, 2,2-bis (4-hydroxyphenyl) propane [bisphenol A]; bis (4-hydroxyphenyl) methane [bisphenol F]; 2,2-bis (4
-Hydroxyphenyl) butane [bisphenol B];
2,2-bis (4-hydroxyphenyl) pentane;
3,3-bis (4-hydroxyphenyl) pentane;
2,2-bis (4-hydroxyphenyl) hexane;
3,3-bis (4-hydroxyphenyl) hexane and the like can be mentioned, and bisphenol A is particularly preferably used. Examples of the tetrahalogenobisphenols represented by the general formula (VI) include tetrabromobisphenol A, tetrachlorobisphenol A, tetrafluorobisphenol A, tetraiodobisphenol A, tetrabromobisphenol F, tetrachlorobisphenol F. , Tetrachlorobisphenol B, and the like, and particularly tetrabromobisphenol A is preferably used. Examples of the polyhalogenophenol represented by the general formula (VII) include, for example, bromophenol, chlorophenol, fluorophenol, dibromophenol, dichlorophenol, difluorophenol, tribromophenol, trichlorophenol, trifluorophenol, and tetrafluorophenol. Examples thereof include bromophenol, tetrachlorophenol, tetrafluorophenol, pentabromophenol, pentachlorophenol and pentafluorophenol, with tribromophenol being particularly preferred. In addition, a part (50 mol% or less) of the polyhalogenophenol may be changed to a monohydric phenol such as p-tert-butylphenol or phenol. Further, other examples of the catalyst include tributylamine, tetramethylammonium chloride, tetraethylammonium chloride, tetrabutylammonium chloride, trimethylphenylammonium chloride, triethylphenylammonium chloride, tetrabutylammonium bromide, and the like. Triethylamine is preferred. In addition, as the alkaline aqueous solution, sodium hydroxide, potassium hydroxide,
An aqueous solution of an alkaline compound such as sodium carbonate can be used.

After the reaction is completed, the reaction mixture thus obtained is separated into an aqueous phase and an organic phase containing the PC copolymerized oligomer by stationary separation or centrifugation, and the organic phase containing the PC copolymerized oligomer is separated. The phase may be taken out or the next step may be performed without phase separation. The PC copolymerized oligomer contained in the reaction mixture or the separated organic phase is then treated with a polyorganosiloxane (PDMS) corresponding to the structural unit III represented by the general formula (III).
It is possible to produce a PC-PDMS copolymer by mixing and under the condition that substantially no alkaline compound is present, and further reacting bisphenols in the presence of the alkaline compound. Here, the polyorganosiloxane (for example, PDMS) corresponding to the structural unit III is
There are various ones, but the general formula (VIII) is preferable.

[0024]

[Chemical 12]

The PDMS is represented by and is highly reactive.
Here, R ^{5 to} R ⁸ each represent hydrogen, an alkyl group having 1 to 6 carbon atoms, or a phenyl group, and may be the same or different. Further, in one molecule, k R ^{5 s} and k R ^{6 s} may be the same or different. And R ⁹ and R
¹⁰ represents an organic residue containing an aliphatic or aromatic group, and Z represents a hydroxyl group, an amino group, a carboxyl group, an acid chloride or a phenolic hydroxyl group. k is an integer of 1 to 100, preferably 5 to 50. Here, when k exceeds 100, the transparency of the obtained PC-PDMS copolymer decreases. In the production of the PC-PDMS copolymer, the above-mentioned PDMS is the PC copolymer oligomer (solid amount) 10
Weight ratio of 0.01 to 14 with respect to 0, preferably 0.0
The reaction is carried out at a ratio of 2-12. The bisphenols are reacted at a molar ratio of 10 to 30 with respect to 100 bisphenol units in the PC oligomer. The tetrahalogenobisphenols, polyhalogenophenols, and bisphenols are added as an aqueous alkali solution, and PDMS is added as it is or as a methylene chloride solution, but the order of addition is not particularly limited. However, it is desirable that the bisphenols be added last. The reaction time is 30 minutes to 2 hours, and the reaction temperature is 20 to 40 ° C.

The PC-PDMS copolymer of the present invention contains the PC copolymer oligomer having the repeating units I and II and the PDMS corresponding to the structural unit III under the condition that substantially no alkaline compound is present. Mix under
It is produced by reacting in the presence of an alkaline compound and a catalyst, and then reacting with bisphenols. That is, in order to produce the PC-PDMS copolymer of the present invention, first, a PC copolymer oligomer and PDMS are prepared.
And are mixed with an organic solvent (for example, methylene chloride) in a mixer under the condition that substantially no alkaline compound is present. Here, the mixer is not particularly limited as long as it can mix fluids, and may be a vertical type or a horizontal type, and may be a dynamic mixer or a static mixer. Also,
It may be an orifice or a centrifugal pump.
Specific examples of the dynamic mixer include, for example, multi-line mixer [manufactured by Satake Chemical Industry Co., Ltd.], Komatsu through the disintegrator [manufactured by Komatsu Zenoa Co., Ltd.], pipeline homomixer [special machinery industry ( Co., Ltd.] and the like. Specific examples of the static mixer include a Kenix type static mixer, a Sulzer type static mixer, and a Toray type static mixer.

The mixture of PC copolymerized oligomer and PDMS mixed in this mixer is then reacted with bisphenols in the presence of an alkaline compound and a catalyst in the reactor to react the PC-PDMS copolymer. The product can be obtained. Alternatively, the mixture of PC copolymerized oligomer and PDMS mixed in this mixer is then reacted in the reactor in the presence of an alkaline compound and a catalyst to form a PC-PDMS copolymerized oligomer. Furthermore, by reacting this PC-PDMS copolymer oligomer with bisphenol in the presence of an alkaline compound and a catalyst, PC-
It is also possible to obtain a reaction product of a PDMS copolymer. Here, the bisphenols include, as a part thereof, the general formula
Tetrahalogenobisphenols represented by (VI) can be used. This PC copolymer oligomer and PDMS
The reaction product of the PC-PDMS copolymer obtained by the reaction with is because the PC copolymer oligomer is in excess in a molar amount, and therefore, the PC-PDMS copolymer oligomer in which the PC copolymer oligomer is reacted with both terminals of PDMS is used. It is a mixture of PC copolymer oligomers. Here, the reactor is not particularly limited as long as it can stir the fluid, and may be a vertical type or a horizontal type. For example, there is a pipeline homomixer [made by Tokushu Kika Kogyo Co., Ltd.]. The reaction temperature in this reactor is 0 to 60 ° C, preferably 10
~ 50 ° C. The reaction residence time may be 1 second or longer.

The above-mentioned PC-PDMS copolymer or P
Examples of the alkaline compound used to obtain the C-PDMS copolymerized oligomer include NaOH and KOH. This alkaline compound has a molar ratio of 1 to 20, preferably 1.1 to PDMS end groups.
10 added. If the alkaline compound is less than 1, PC
It is not preferable because the reaction between the copolymer oligomer and PDMS does not proceed completely. In addition, the alkaline compound is 20
If it exceeds, the decomposition of the chloroformate group of the PC copolymer oligomer increases, and the molecular weight of the resulting PC-PDMS copolymer does not improve, which is not preferable.

The catalyst may be a tertiary amine or
Can use a quaternary ammonium salt. concrete
Examples of the tertiary amine include trimethylamido.
And triethylamine, tripropylamine, etc.
Be done. Further, as the quaternary ammonium salt, for example,
Trimethylbenzylammonium chloride, triethyl
And rubenzyl ammonium chloride. This
The amount of the catalyst added is equal to that of the PC copolymer oligomer chlorophore.
The molar ratio to the mate group is 1.0 × 10^-Four~ 5.0 x 1
0^-2, Preferably 5.0 × 10^-Four~ 1.0 x 10 ^-2Is.
Addition amount is 1.0 × 10^-FourWhen the value is less than 1, the reaction progresses slowly and
It was 5.0 × 10^-2If it exceeds, the effect will be
No fruit is seen and it is not necessary to add more than this.

On the other hand, the rubber-like elastic body of the component (B) constituting the polycarbonate resin composition of the present invention is not particularly limited, and various kinds can be used, and the following ones can be preferably used. For example, there is a resin polymer obtained by polymerizing one or more vinyl-based monomers in the presence of a rubber-like polymer mainly containing alkyl acrylate and / or alkyl methacrylate. Here, as the alkyl acrylate or alkyl methacrylate, those having an alkyl group having 2 to 10 carbon atoms are preferable. Specifically, ethyl acrylate, butyl acrylate, 2-ethylhexyl acrylate, n-
Examples include octyl methacrylate. The rubbery polymer mainly containing these alkyl acrylates means 70% by weight or more of the alkyl acrylates and other vinyl-based monomers copolymerizable therewith, such as methyl methacrylate, acrylonitrile, vinyl acetate and styrene. Etc. 30
It means a polymer obtained by reacting with less than or equal to wt%.
In this case, a polymer obtained by appropriately adding and reacting a polyfunctional monomer such as divinylbenzene, ethylene dimethacrylate, triallyl cyanurate, triallyl isocyanurate as a crosslinking agent is also included. Examples of the vinyl-based monomer reacted in the presence of the rubbery polymer include aromatic vinyl compounds such as styrene and α-methylstyrene, acrylic acid esters such as methyl acrylate and ethyl acrylate, methyl methacrylate and methacrylic acid. Examples include monomers such as methacrylic acid esters such as ethyl acidate, and one or more of these monomers are polymerized in the presence of a rubber-like polymer. Further, these monomers are copolymerized with other vinyl type monomers such as vinyl cyanide compounds such as acrylonitrile and methacrylonitrile, vinyl esters such as vinyl acetate and vinyl propionate. Here, the polymerization reaction can be carried out by various methods such as bulk polymerization, suspension polymerization and emulsion polymerization, and those produced by emulsion polymerization are particularly preferable. The polymer thus obtained preferably contains 20% by weight or more of the rubber component. As such a polymer, specifically, 60
~ 80 wt% n-butyl acrylate and styrene,
An MAS resin elastic body such as a graft copolymer with methyl methacrylate may be used. Examples of the above MAS resin elastic body include trade name "KM-330" manufactured by Rohm & Haas Co., Ltd., trade name "METABLEN S2001" manufactured by Mitsubishi Rayon Co., Ltd., and the like.

Further, a copolymer obtained by copolymerizing an alkyl acrylate and / or an alkyl methacrylate with a polyfunctional polymerizable monomer having a conjugated diene type double bond is added to a copolymer of vinyl type monomer 1 There are polymers obtained by polymerizing two or more species. Here, the above-mentioned ones are used as the alkyl acrylate and the alkyl methacrylate. In addition, as the polyfunctional polymerizable monomer having a conjugated diene type double bond, a conjugated diene compound such as isoprene or butadiene, or a non-conjugated double bond other than the conjugated diene type double bond in one molecule may be used. Compounds that have. Specific examples of such a compound include 1-methyl-2-vinyl4,5-heptadien-1-ol; 7-
Methyl-3-methylene-1,6-octadiene; 1,
3,7-octatriene and the like. When copolymerizing the above-mentioned alkyl acrylate and / or alkyl methacrylate with a polyfunctional polymerizable monomer having a conjugated diene type double bond, styrene, an aromatic vinyl compound such as α-methylstyrene, if necessary, Add vinyl cyanide compounds such as acrylonitrile and methacrylonitrile, vinyl ester compounds such as vinyl acetate and vinyl propionate, vinyl ether compounds such as methyl vinyl ether, and vinyl monomers such as vinyl halide compounds such as vinyl chloride. You can also Further, a crosslinking agent such as ethylene dimethacrylate or divinylbenzene may be added.
When the above-mentioned alkyl acrylate and / or alkyl methacrylate is copolymerized with a polyfunctional polymerizable monomer having a conjugated diene type double bond to produce a copolymer, the conjugated diene type double bond is The polyfunctional polymerizable monomer has 0.1 to 20% by weight in the copolymer, preferably 1 to
It should be used in a proportion of 10% by weight. Examples of the vinyl-based monomer to be polymerized with the copolymer thus obtained include those mentioned above, and one or more of these are used. Here, the polymerization reaction can be carried out by various methods such as bulk polymerization, suspension polymerization and emulsion polymerization, and those produced by emulsion polymerization are particularly preferable.

The polymer (rubber-like elastic material) obtained as described above can be used as the component (B) of the present invention. Preferred examples of such a rubber-like elastic body are shown below. Firstly, an alkyl (meth) acrylate such as n-butyl acrylate, 2-ethylhexyl acrylate or methyl methacrylate and butadiene are copolymerized by a conventional method with a small amount of a cross-linking agent such as ethylene dimethacrylate or divinylbenzene. There is a graft copolymer obtained by adding a vinyl-based monomer such as styrene, acrylonitrile, or vinyl chloride as a graft component monomer to the obtained latex and graft-polymerizing it by a conventional method.

The second is obtained by copolymerizing the above alkyl (meth) acrylate with a compound having a non-conjugated double bond in addition to a conjugated diene type double bond in one molecule by a conventional method. There is a graft copolymer obtained by adding the above-mentioned vinyl-based monomer as a graft component monomer to the latex and graft-polymerizing it by a conventional method. In addition,
Here, the graft polymerization may be carried out in one step, or may be carried out in multiple steps by changing the constituent components of the graft component monomer. More specifically, as such a copolymer, octyl acrylate and butadiene are used in a ratio of the former: the latter = 7: 3 to obtain a rubber latex obtained by copolymerization,
There is a MABS resin elastic body such as a graft copolymer obtained by adding styrene and methyl methacrylate and graft-polymerizing. Further, there is an MBS resin elastic body such as a graft copolymer obtained by graft-polymerizing styrene to rubber latex obtained by copolymerizing methyl methacrylate and butadiene. Examples of the above MBS resin elastic body include "HIA 15" and "HIA" manufactured by Kureha Chemical Industry Co., Ltd.
1A 28 "," H1A 30 "(both are trade names) and the like are preferably used.

Further, other rubber-like elastic bodies, for example,
ABS resin elastic body, natural rubber (NR) or styrene-butadiene rubber (SBR), polybutadiene rubber (B
R), isoprene rubber (IR), acrylonitrile-butadiene rubber (NBR), acrylonitrile-isoprene rubber (NIR), chloroprene rubber (CR), or other diene rubber or isobutylene-isopropylene rubber (I
IR), ethylene-propylene rubber (EPM), ethylene-propylene-diene rubber (EPDM), chlorosulphonated polyethylene rubber (CSM), ethylene-vinyl acetate rubber (EVM), and other olefin rubbers, as well as various acrylic rubbers, Other examples include organic silicon compound type rubber, organic fluorine compound type rubber, urethane type rubber, ether type rubber and the like.

The resin composition of the present invention comprises the above-mentioned component (A).
And the component (B), and the mixing ratio of the respective components is PC-PDMS copolymer 1 which is the component (A).
~ 99 wt%, preferably 50-95 wt% and (B)
The component is a polyamide resin 99 to 1% by weight, preferably 50 to 5% by weight. If the amount of the PC-PDMS copolymer as the component (A) is less than 1% by weight, the flame retardancy is poor. Further, if it exceeds 99% by weight, the fluidity is poor. The amount of polyorganosiloxane in the resin composition is 0.01% by weight or more. If the amount of this polyorganosiloxane is less than 0.01% by weight, the flame retardancy will not be 1/16 inch V-0.

The resin composition of the present invention may be mixed with a commercially available polycarbonate resin, other synthetic resin, or an elastomer as the component (C), if necessary, within the range not impairing the object of the present invention. You may use. Further, an inorganic filler, various additives and the like can be blended. Examples of the synthetic resin include polyethylene, polypropylene, polystyrene, acrylonitrile-styrene (AS) resin, acrylonitrile-butadiene-styrene (ABS) resin, polymethylmethacrylate, polyester, and polyamide. Examples of the elastomer include isobutylene-isopropylene rubber, styrene-butadiene rubber, ethylene-propylene rubber, acrylic elastomer and the like.

Various inorganic fillers can be used. Specifically, glass, carbon fiber, and other inorganic fillers are used. First, as the glass material, for example, glass fiber, glass beads, glass flakes, glass powder or the like can be used. Here, the glass fiber used may be any of alkali-containing glass, low-alkali glass and non-alkali glass. Its fiber length is 0.1 to 8 mm, preferably 0.1.
3 to 6 mm, and the fiber diameter is 0.1 to 30 μm,
It is preferably 0.5 to 25 μm. And the form of this glass fiber is not particularly limited, for example, roving,
There are various types such as milled fiber and chopped strand. These glass fibers may be used alone or in combination of two or more. These glass materials are surface-treated with a silane coupling agent such as aminosilane, epoxysilane, vinylsilane or methacrylsilane, a chromium complex compound or a boron compound in order to enhance the affinity with the resin. It may be one. As such a glass material, for example, commercially available MA-4 manufactured by Asahi Fiber Glass Co., Ltd.
09C (average fiber diameter 13 μm) or TA-409C
(Average fiber diameter 23 μm) and the like can be preferably used.

Next, the carbon fibers used are generally those produced by firing using cellulose fibers, acrylic fibers, lignin, petroleum or coal-based pitch as a raw material, and are flame resistant, carbonaceous or There are various types such as graphite. The fiber length of the carbon fiber is usually 0.01 to 10 mm, preferably 0.02 to 8 m.
The fiber diameter is in the range of m, and the fiber diameter is 1 to 15 μm, preferably 5 to 13 μm. The form of the carbon fiber is not particularly limited, and examples thereof include various types such as roving, milled fiber, chopped strand, and strand. These glass fibers may be used alone or in combination of two or more. The surface of these carbon fibers, in order to increase the affinity with the resin,
It may be one that has been surface-treated with an epoxy resin or a urethane resin. As such a carbon fiber, for example, a commercially available product such as Vesphite (average fiber diameter 7 μm) manufactured by Toho Rayon Co., Ltd. can be preferably used.

Other inorganic fillers include, for example, aluminum fiber, calcium carbonate, magnesium carbonate,
Dolomite, silica, diatomaceous earth, alumina, iron oxide, zinc oxide, magnesium oxide, calcium sulfate, magnesium sulfate, calcium sulfite, talc, clay, mica,
Asbestos, calcium silicate, montmorillonite, bentonite, carbon black, graphite, iron powder, lead powder, aluminum powder and the like can also be used.

Further, various additives include antioxidants such as hindered phenol-based, phosphite-based, and phosphoric acid-based antioxidants, ultraviolet absorbers such as benzotriazole-based and benzophenone-based antioxidants, and hindered amine-based light sources. Examples thereof include stabilizers, internal lubricants such as aliphatic carboxylic acid esters, paraffin, silicone oil and polyethylene wax, flame retardants, flame retardant aids, antistatic agents and colorants.

The resin composition of the present invention comprises the above-mentioned component (A).
And the component (B) and, if necessary, the component (C),
It can be obtained by kneading. Then, for the compounding and kneading, a method usually used, for example, a ribbon blender, a Henschel mixer, a Banbury mixer, a drum tumbler, a single screw extruder, a twin screw extruder, a co-kneader, a multi-screw extruder, etc. Can be done using. The heating temperature for kneading is usually selected in the range of 250 to 300 ° C. The polycarbonate resin composition thus obtained can be applied to various known molding methods such as injection molding, blow molding, extrusion molding, compression molding, calender molding, rotational molding, etc. to produce various molded articles. Can be used for

The resin composition of the present invention comprises a tetrahalogenobi
Sphenol or polyhalogenophenol
By blending PC-PDMS copolymer with flame retardancy
Therefore, it is possible to obtain a molded product with sufficient flame retardancy.
Wear. Furthermore, by adding a flame retardant, it becomes even more flame retardant.
It is possible to impart sex. Add even more flame retardancy
The flame retardant used to
Alkali metal salts or alkaline earth metal salts of inorganic acids, and
And halogen-containing compounds. Where preferred
As the inorganic alkali metal salt, sodium salt, potassium salt
Examples thereof include salts and lithium salts. In addition, inorganic alkali
Examples of earth metal salts include calcium salts and magnesium salts.
Is mentioned. Also, an inorganic alkali metal salt or inorganic acid
As an inorganic acid used to obtain Lucari earth metal salts
Is H₃AlF₆, H₃BF₆, H₃SbF₆, H₂T
iF₆, H₂SiF₆, H₃PO_Four, H₂ZrF ₆, H
₂WF₆, HBF_FourEtc. Preferred inorganic al
Examples of potassium metal salts or inorganic alkaline earth metal salts include N
a₃AlF₆, Ca₃(AlF₆)₂Is mentioned. Also,
Obtain an organic alkali metal salt or an organic alkaline earth metal salt
The preferred organic acid used in the
Fonic acid, aromatic sulfonic acid, aromatic carboxylic acid and fat
It is an aliphatic carboxylic acid. As a specific example, trifluoro
Methane-sulfonic acid; Perfluorobutane sulfonic acid;
Perfluorooctane sulfonic acid; dodecane sulfone
Acid; benzenesulfonic acid; 2,4,6-trichloroben
Zensulfonic acid; benzenedisulfonic acid; naphthols
Rufonic acid; caprylic acid; lauric acid; benzoic acid; naphtho
Carboxylic acid; 2,4,6-tribromobenzoic acid, etc.
Can be mentioned. Preferred organic alkali metal salt or organic acid
Perfluorobutane sulfo is used as the alkaline earth metal salt.
Potassium phosphate, calcium perfluorobutane sulfonate
Mu. Further, as the halogen-containing compound,
Various types can be used. With its representative
Contains tetrahalogenobisphenols
Low molecular weight polycarbonate, tetrahalogenobisphe
Epoxy resin and other halo containing nols
Gen-based flame retardants can be mentioned. Among them, especially on
Flame retardants belonging to the above item are preferable.

Here, the low molecular weight polycarbonate containing the above tetrahalogenobisphenols has the general formula

[0044]

[Chemical 13]

[Wherein, X ^{6 to} X ⁹ represent a halogen atom, R ¹¹ represents an alkylene group having 2 to 8 carbon atoms, and 1 to 9 carbon atoms.
Represents an alkylidene group, a carbonyl group, a sulfone group, a sulfur atom or an oxygen atom. ] The repeating unit (X) represented by

[0046]

[Chemical 14]

[In the formula, R ¹¹ is the same as defined above. ] The repeating unit (Y) represented by q pieces [however, p shows the integer of 1-30, q shows the integer of 0-30, p + q = 1-50]
It is an integer of (particularly 3 to 20). ], And is represented by a low molecular weight polycarbonate (polycarbonate oligomer) having a halogen content of 30% by weight or more. Here, as the halogen-containing bisphenol compound constituting the repeating unit (X), 2,2-bis (3,3
5-dibromo-4-hydroxyphenyl) propane;
2,2-bis (3,5-dichloro-4-hydroxyphenyl) propane; bis (3,5-dibromo-4-hydroxyphenyl) methane; bis (3,5-dibromo-4-)
Hydroxyphenyl) ether; bis (3,5-dibromo-4-hydroxyphenyl) sulfone and the like are used,
Especially, 2,2-bis (3,5-dibromo-4-hydroxyphenyl) propane [commonly known as tetrabromobisphenol A] is effective. Further, as the bisphenol compound constituting the repeating unit (Y), 2,2-bis (4-
Hydroxyphenyl) propane; bis (4-hydroxyphenyl) methane; bis (4-hydroxyphenyl) sulfone; bis (4-hydroxyphenyl) ether and the like are used, and particularly 2,2-bis (4-hydroxyphenyl) propane. [Common name bisphenol A] is effective.

Next, the epoxy resin containing tetrahalogenobisphenols has the general formula

[0049]

[Chemical 15]

[Wherein R ¹¹ is the same as defined above, R ¹² represents a hydrogen atom, a methyl group, an epoxypropyl group, a phenyl group, a 2-hydroxypropyl group or an oxygen atom, and X ^{10 to} X ¹³ are halogens. Represents an atom, and r represents an integer of 1 to 30. ] And a halogen content of 30% by weight or more.

Other halogen-based flame retardants include, for example, tetrabromobenzene; tetrachlorobenzene; hexabromobenzene; hexachlorobenzene; hexabromobiphenyl; octabromobiphenyl; 2,2'-dichlorobiphenyl; 2,4 '. -Dibromobiphenyl; 2,4'-dichlorobiphenyl;hexabromobiphenyl; triphenyl chloride; tetrachlorophthalic acid; tetrachlorophthalic anhydride; tetrabromophthalic acid; tetrabromophthalic anhydride; tribromophenol and other known There are halogenated aromatic compounds and also 2,2-bis (3,5-dichlorophenyl) propane; bis (2-chlorophenyl) methane; bis (2,6-dibromophenyl) methane;
-Bis (2,6-dichlorophenyl) ethane; 1,1-
Bis (2-chloro-4-methylphenyl) ethane; 1,
1-bis (3,5-dichlorophenyl) ethane; 2,2
-Bis (3-phenyl-4-bromophenyl) ethane;
2,3-bis (4,6-dichloronaphthyl) propane;
2,2-bis (2,6-dichlorophenyl) pentane;
2,2-bis (2,6-dichlorophenyl) hexane;
Bis (4-chlorophenyl) methane; Bis (3,5-dichlorophenyl) cyclohexylmethane; Bis (3-nitro-4-bromophenyl) ethane; Bis (4-hydroxy-2,6-dichloro-3-methoxyphenyl) methane 2,2-bis (3,5-dichloro-4-hydroxyphenyl) propane; 2,2-bis (3,5-dibromo-4-hydroxyphenyl) propane; 2,2-bis (3-bromo-4) -Hydroxyphenyl) propane;
There are diaromatics such as 2,2-bis (3,5-dibromo-4-hydroxyphenyl) propane diglycidyl ether. Further, halogenated diphenyl ethers, particularly those containing 2 to 10 halogen atoms are preferable, and examples thereof include decabromodiphenyl ether, octabromodiphenyl ether, hexabromodiphenyl ether, pentabromodiphenyl ether, tetrabromodiphenyl ether, tribromodiphenyl ether, dibromodiphenyl ether, hexachloro. Examples include diphenyl ether, pentachlorodiphenyl ether, tetrachlorodiphenyl ether, trichlorodiphenyl ether and dichlorodiphenyl ether.

[0052]

The present invention will be further described in detail with reference to production examples, examples and comparative examples. Production Example 1-1 [Production of Polycarbonate Oligomer A] 60 kg of bisphenol A was dissolved in 400 liters of a 5 wt% sodium hydroxide aqueous solution to prepare a sodium hydroxide aqueous solution of bisphenol A. Then, the aqueous sodium hydroxide solution of bisphenol A kept at room temperature was passed through the orifice plate at a flow rate of 138 liters / hour and methylene chloride at a flow rate of 69 liters / hour through a tubular reactor having an inner diameter of 10 mm and a tube length of 10 m. It was introduced, and phosgene was co-currently flown thereinto and blown at a flow rate of 10.7 kg / hour to continuously react for 3 hours. The tubular reactor used here was a double tube, and cooling water was passed through the jacket to keep the discharge temperature of the reaction solution at 25 ° C. Further, the pH of the discharged liquid was adjusted so as to show 10 to 11. The reaction liquid thus obtained was allowed to stand still to separate and remove the aqueous phase, and a methylene chloride phase (220 liters) was collected. To this, 170 liters of methylene chloride was further added and sufficiently stirred. Polycarbonate oligomer A (concentration 3
17 g / liter). The polycarbonate oligomer A obtained here had a degree of polymerization of 2 to 4 and a chloroformate group concentration of 0.7N.

Production Example 1-2 [Production of Polycarbonate Oligomer B] 2,275 g (9.96 mol) of bisphenol A was dissolved in 14 liters of 2.0N aqueous sodium hydroxide solution, and the mixture was placed in a vessel having an internal volume of 50 liters equipped with a stirrer. After adding 8.25 liters of methylene chloride and stirring (50 rpm), phosgene was blown at a flow rate of 0.2 mol / min for 70 minutes while cooling to carry out the reaction.
After stopping the blowing of phosgene, stirring was continued for another 30 minutes. Then, tetrabromobisphenol A25
0 g (0.46 mol), tribromophenol 150 g
(0.453 mol) sodium hydroxide (NaOH: 78.
6 g, water: 1.35 liters) was added while continuing stirring, and triethylamine (1.8 cc) was added,
The reaction was carried out at 450 rpm for 60 minutes. After the reaction, the mixture was allowed to stand for about 30 minutes and the aqueous phase was separated to obtain an organic phase. Polycarbonate oligomer B (concentration: 500 g / liter,
Chloroformate group concentration: 0.5 mol / liter).

Production Example 2-1 [Synthesis of Reactive PDMS-A] 1,483 g of octamethylcyclotetrasiloxane, 96 g of 1,1,3,3-tetramethyldisiloxane and 35 g of 86% sulfuric acid were mixed. The mixture was stirred at room temperature for 17 hours. Then the oil phase is separated and
g of sodium hydrogen carbonate was added, and the mixture was stirred for 1 hour. After filtration, vacuum distillation was performed at 150 ° C. and 3 torr to remove low-boiling substances to obtain oil. 60 g of 2-allylphenol and 0.00
In a mixture with 14 g of platinum chloride-platinum as an alcoholate complex, 294 g of the oil obtained above was added at 90 ° C.
Was added at the temperature of. The mixture was stirred for 3 hours while maintaining the temperature of 90 to 115 ° C. The product was extracted with methylene chloride and washed 3 times with 80% aqueous methanol to remove excess 2-allylphenol. The product was dried over anhydrous sodium sulphate and evaporated in vacuo to a temperature of 115 ° C. The obtained terminal phenol PDMS is NM
By measurement of R, the number of repeating dimethylsilanooxy units was 30.

Production Example 2-2 [Synthesis of Reactive PDMS-B] In Production Example 2-1
The procedure of Production Example 2-1 was repeated, except that the amount of 1,1,3,3-tetramethyldisiloxane was changed to 18.1 g. In the obtained terminal phenol PDMS, the number of repeating dimethylsilanooxy units was 150 as measured by NMR.

Production Example 2-3 [Synthesis of Reactive PDMS-C] In Production Example 2-1
Example 1 was repeated except that the amount of 1,1,3,3-tetramethyldisiloxane was changed to 7.72 g. In the obtained terminal phenol PDMS, the number of repeating dimethylsilanooxy units was 350 as determined by NMR.

Production Example 3-1 [Production of PC-PDMS Copolymer A ₁ ] In a vessel equipped with a stirrer and having an internal volume of 50 liters, 10 liters of polycarbonate oligomer A (11.6 mol of bisphenol A unit) and 40 g of reactive PDMS-A were added. What was mixed and dissolved, 330 g (0.61 mol) of tetrabromobisphenol A and 169 g (0.51 mol) of tribromophenol were added to the sodium hydroxide aqueous solution (NaOH: 110 g, water: 1.
35 liters) was mixed, triethylamine (2.9 cc) was added, and the mixture was stirred at 300 rpm for 60 minutes,
It was made to react. After completion of the reaction, 500 g of bisphenol A was added to the above reaction system with an aqueous sodium hydroxide solution (NaOH: 29
0 g, water: 3.42 liters) was mixed and mixed with 6.1 liters of methylene chloride, and 450 minutes for 60 minutes
The mixture was stirred and reacted at rpm. After the reaction, the organic phase and the aqueous phase were separated, and the organic phase was washed and separated in order of alkali (0.01N-NaOH), acid (0.1N-HCl) and water. A flake-shaped polymer was obtained by removing methylene chloride.

Production Example 3-2 [Production of PC-PDMS Copolymer A ₂ ] In the same manner as in Production Example 3-1, except that 160 g of reactive PDMS was used in Production Example 3-1, a flaky shape was obtained. A polymer of

Production Example 3-3 [Production of PC-PDMS Copolymer A ₃ ] The PC oligomer B obtained in Production Example 1-2 and the production example 2-1 were obtained by the flow shown in FIG. 1. Reactive PDMS-A was reacted. PC oligomer B, reactive PDMS-A
5% by weight methylene chloride solution, 1% by weight triethylamine (TEA) aqueous solution and 25% by weight sodium hydroxide (NaOH) aqueous solution were used, respectively. Each flow rate is PC oligomer B: 13 liters / hour, reactive P
DMS-A: 4 liters / hour, TEA: 0.3 liters / hour, and NaOH: 0.23 liters / hour. Pipeline homomixer [made by Tokushu Kika Kogyo Co., Ltd., 2SL type: inner volume 0.3 liter, diameter of first turbine blade 42.5 mm, diameter of second turbine blade 48]
mm], the mixer is 500 rpm, and the reactor is 3,000
It was rotated at 0 rpm. The main pipe (PC oligomer line) used had an inner diameter of 16 mm. TE
A was charged 60 cm from the mixer, and NaOH was charged 80 cm from the mixer. Reactor temperature is 25 ~
It was 30 ° C. The obtained reaction product (containing a PC-PDMS copolymer oligomer) was left standing and separated to obtain an organic phase 330c.
c was transferred to a 1-liter batch type reactor, 120 cc of methylene chloride and 2.2 g of p-tert-butylphenol were added, and the mixture was stirred to make it uniform. An alkaline aqueous solution of bisphenol A (bisphenol A: 19 g, sodium hydroxide: 11 g, water: 130 cc) was added to this, and 500 rpm
And reacted for 1 hour. After the reaction, the mixture was transferred to a 7-liter washing tank, 400 cc of methylene chloride and 400 cc of water were added, and the organic phase and the aqueous phase were separated. After separation, the organic phase is alkali (0.
01N-NaOH) washing, acid (0.1N-HCl) washing,
Wash with water, then remove methylene chloride, then PC-PDMS
Flake of copolymer was obtained.

Production Example 3-4 [Production of PC-PDMS Copolymer A ₄ ] In the same manner as in Production Example 3-1, except that 40 g of reactive PDMS-A was changed to 20 g in Production Example 3-1. A flake-like polymer was obtained.

Production Example 3-5 [Production of PC-PDMS Copolymer A ₅ ] Production Example 3-1 was changed to Production Example 3-1 except that 40 g of reactive PDMS-A was changed to 8 g and 330 g of tetrabromobisphenol A was changed to 195 g. A flake polymer was obtained in the same manner as in Example 3-1.

Production Example 3-6 [Production of PC-PDMS Copolymer A ₆ ] Production Example 3-1 except that reactive PDMS-A was changed to reactive PDMS-B in Production Example 3-1. Similarly, a flake polymer was obtained.

Production Example 3-7 [Production of PC-PDMS Copolymer A ₇ ] Production Example 3-1 except that reactive PDMS-A was changed to reactive PDMS-C in Production Example 3-1. Similarly, a flake polymer was obtained.

Production Example 4-1 [Production of Polycarbonate C ₁ ] Production Example 3-1 except that reactive PDMS was not used in Production Example 3-1.
A flake-shaped polymer was obtained in the same manner as in.

Production Example 4-2 [Production of Polycarbonate C ₂ ] In Production Example 4-1, p-tert was used instead of 169 g of tribromophenol.
-Production Example 3-1 except that 77 g of butylphenol was used
A flake-shaped polymer was obtained in the same manner as in.

PC-PDM obtained in Production Examples 3-1 to 7
The S copolymers A _{1 to} A ₇ and the polycarbonates C _{1 to} C ₂ obtained in Production Examples 4-1 and ₂ are each 1
After drying overnight at 20 ° C., it was pelletized at 280 ° C. by an extruder. Then, for each of the physical property evaluations, P
The DMS content, Br content and viscosity average molecular weight were measured.
The results are shown in Table 1. When preparing the pellets, 800 ppm of trisnonylphenylphosphite was added as an antioxidant to the PC-PDMS copolymers A ₁ and A ₂ and the polycarbonate C ₁ . Also, PC-P
For DMS copolymer A ₃ , 1,000 pp of potassium perfluorobutylsulfonate [Megafax F114: C ₄ F ₉ SO ₃ K manufactured by Dainippon Ink and Chemicals, Inc.] was used as a flame retardant.
m was added. Then, PC-PDMS copolymer A ₄ was prepared by adding 5,0 stearic acid monoglyceride as a lubricant.
00 ppm was added.

[0067]

[Table 1]

The PDMS content, Br content and viscosity average molecular weight were measured as follows. 1: of aromatic H of bisphenol A residue found at 7.1 to 7.3 ppm by PDMS ¹ HNMR, aromatic H of TBA residue found at 7.43 ppm and methyl H of PTBP found at 0.11 ppm It was calculated from the strength ratio. 2: Br content (total Br content in the copolymer) The sample was alkali decomposed and analyzed by the Horhard method. 3: Viscosity average molecular weight (Mv) The viscosity of the methylene chloride solution at 20 ° C was measured using an Ubbelohde type viscosity tube, and the intrinsic viscosity [η] was calculated from this, and then calculated by the following formula. [Η] = 1.23 × 10 ⁻⁵ × Mv ^0.83

Examples 1 to 13 and Comparative Examples 1 to 10 PC-PDMS copolymer A obtained in Production Examples 3-1 to 7
_{1 to} A ₇ and the polycarbonates C _{1 to} C ₂ obtained in Production Examples 4-1 and ₂ were dried at 120 ° C. for a whole day and night, and then, as non-halogen-containing polycarbonates, commercially available polycarbonate C ₃ and rubber-like elastic body B _{1 were used.} , B ₂ , B ₃ , B ₄ ,
B ₅ and B ₆ were premixed with a dry tumbler in a mixing ratio shown in Table 2, then fed to an extruder, kneaded at 270 ° C., and pelletized. The resulting pellets are each 1
After drying at 20 ° C. for 12 hours, injection molding was performed to obtain a test piece. About the obtained test piece, as its quality evaluation,
Tensile strength, Izod impact strength, flame retardancy and flow value were measured. The results are shown in Table 3. The rubber-like elastic body is as follows. B _1: MAS rubber [US Rohm & Haas Co. Paraloid KM330] B _2: MBS rubber [Kureha Chemical Co., Ltd., HIA-15] B _3: isobutylene - isopropylene rubber [JSR Co., Butyl 268] B ₄ : EPDM rubber [manufactured by Nippon Synthetic Rubber Co., Ltd., EP59
P] B _5: SBS rubber [Shell Chemical Co., Ltd., potassium Rex TR1101] B _6: MAS rubber [Mitsubishi Rayon Co., Ltd., METABLEN S-2001] Further, commercially available polycarbonate are as follows. C _3: Tarflon A2200 [Idemitsu Petrochemical Co., Ltd., M
v: 21,500]

[0070]

[Table 2]

[0071]

[Table 3]

[0072]

[Table 4]

[0073]

[Table 5]

Each measurement was performed as follows. 1: Tensile strength Measured according to JIS-K-7113. 2: Izod impact strength (with notch) Using a test piece with a thickness of 1/8 inch, JIS-K-711
It measured based on 0. 3: Flame retardancy flame retardancy test UL-94 1/16 inch, 1/32 inch (thickness) A vertical flammability test was conducted in accordance with Underwriters Laboratory Subject 94. 4: Flow value Measured according to JIS-K-7210.

Examples 14 to 17 and Comparative Examples 11 to 14 PC-PDMS copolymer, polycarbonate, rubber-like elastic material and inorganic filler were blended in the proportions shown in Table 4, kneaded at a temperature of 270 ° C., and pelletized. Turned into In addition, the inorganic filler was also supplied from the downstream side near the hopper supply position of the raw material resin of the extruder. The resulting pellets are 1 at 120 ° C each
After drying for 2 hours, injection molding was performed to obtain a test piece. For the obtained test pieces, the tensile strength,
The Izod impact strength, flame retardancy and flow value were measured. The results are shown in Table 5. The inorganic filler is as follows. D ₁ : Glass fiber [Asahi Fiber Glass Co., Ltd., MA
-409C] D _2: carbon fiber [Toho Rayon Co., Ltd., HTA-C6
-SRS] D _3: Talc average diameter 0.9 .mu.m D _4: Calcium carbonate [Shiraishi Kogyo Co., Vigot-10]

[0076]

[Table 6]

[0077]

[Table 7]

[0078]

As described above, the polycarbonate resin composition of the present invention is excellent in flame retardancy, mechanical strength, fluidity and releasability. Therefore, the polycarbonate resin composition of the present invention can be widely and effectively used for various molded articles, for example, flame-retardant parts such as building materials, household appliances, and office automation equipment.

[Brief description of drawings]

FIG. 1 is a diagram showing a production flow of a polycarbonate-polyorganosiloxane copolymer in Production Example 3-3.

Claims (1)

[Claims] 1. The main chain (A) is (a) a compound represented by the general formula (I):[In the formula, R¹And R²Are hydrogen atom or carbon respectively
Represents an alkyl group of the numbers 1 to 4, even if they are the same
It may be different. ] The repeating unit represented by
I, (b) General formula (II)[In the formula, R³And R^FourAre hydrogen atom or carbon respectively
Represents an alkyl group of the numbers 1 to 4, even if they are the same
It may be different. Also, X¹~ X^FourIs that
Is a halogen atom. ] The repeating unit II and
(C) General formula (III):[In the formula, R^Five~ R⁸Are hydrogen atom and carbon number 1 to
6 alkyl groups or phenyl groups, which are the same for each
Or may be different. Also, R ⁹as well as
R^TenIs an organic residue containing aliphatic or aromatic, respectively.
A represents -O-, -NH- or a single bond. k is
It is an integer of 1 to 500. ] The structural unit III represented by
In addition to having the general formula (IV)[In the formula, X^FiveRepresents a halogen atom, m is an integer of 1 to 5
Is. When m is plural, plural X^FiveAre each
It may be the same or different. ]]
Polyhalogenophenoxy group consisting of terminal group IV
Carbonate-polyorganosiloxane copolymer 1-99
% And (B) rubber-like elastic material 99 to 1% by weight
A polycarbonate resin composition comprising: