JPH01247456A - Polycarbonate resin composition - Google Patents

Polycarbonate resin composition

Info

Publication number
JPH01247456A
JPH01247456A JP7314888A JP7314888A JPH01247456A JP H01247456 A JPH01247456 A JP H01247456A JP 7314888 A JP7314888 A JP 7314888A JP 7314888 A JP7314888 A JP 7314888A JP H01247456 A JPH01247456 A JP H01247456A
Authority
JP
Japan
Prior art keywords
polycarbonate resin
weight
glass fiber
resin composition
organopolysiloxane
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP7314888A
Other languages
Japanese (ja)
Other versions
JPH0733474B2 (en
Inventor
Hitoshi Yasumura
安村 均
Yuji Kohama
裕司 小濱
Teruhiko Nakazato
中里 照彦
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Idemitsu Petrochemical Co Ltd
Original Assignee
Idemitsu Petrochemical Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Idemitsu Petrochemical Co Ltd filed Critical Idemitsu Petrochemical Co Ltd
Priority to JP63073148A priority Critical patent/JPH0733474B2/en
Publication of JPH01247456A publication Critical patent/JPH01247456A/en
Publication of JPH0733474B2 publication Critical patent/JPH0733474B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Abstract

PURPOSE:To obtain a polycarbonate resin composition improved in mold release without detriment to the appearance of a molding, by mixing a polycarbonate resin with a glass fiber and an organopolysiloxane. CONSTITUTION:50-97wt.% polycarbonate resin of a viscosity-average MW of 10000-100000 is mixed with 3-50wt.% glass fiber of a fiber diameter of 6-20mum and a fiber length of 1.5-6mm and 0.5-0.4wt.% organopolysiloxane of the formula (wherein R<1-3> are each H, a 1-6C alkyl or phenyl, and m and n are each 0 or >=1), having a viscosity of 5-100000cst at 25 deg.C.

Description

【発明の詳細な説明】 [産業上の利用分野] 本発明はポリカーボネート樹脂組成物に関し、詳しくは
成形品の外観を損わずに離型性に優わたガラス繊維強化
ポリカーボネート樹脂組成物に関するものである。
[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to a polycarbonate resin composition, and more particularly to a glass fiber reinforced polycarbonate resin composition that has excellent mold releasability without impairing the appearance of molded products. be.

[従来の技術、発明が解決しようとする課題]ポリカー
ボネート樹脂は機械的強度、電気的特L I明性などに
侵ね、エンジニアリングプラスチックとし5て様々な分
野で利用されている。特にガラス繊維強化ポリカーボネ
ート樹脂は機へ的強度がさらに改善され、各種工業部材
に使用されている。
[Prior Art and Problems to be Solved by the Invention] Polycarbonate resins have poor mechanical strength, electrical properties, LI clarity, etc., and are used in various fields as engineering plastics5. In particular, glass fiber reinforced polycarbonate resin has further improved mechanical strength and is used in various industrial parts.

しかし、その用途の拡大に伴って工業部品の形状が複雑
化しており、該ガラス繊維強化ポリカーボネート樹脂の
成形に際して離型不良という問題が発生するようになっ
てきた。そこで、該樹脂の離型性や剛性1寸法安定性等
を改善する目的でオルガノポリシロキサンを配合した組
成物が提案されている(特公昭59−35929号公報
)。ところが、この組成物を用いて得られる成形品はガ
ラス繊維の浮きが多く、外観の良好な製品が得られない
どう新たな問題がある。
However, with the expansion of its uses, the shapes of industrial parts have become more complex, and the problem of poor mold release has started to occur when molding the glass fiber reinforced polycarbonate resin. Therefore, a composition containing organopolysiloxane has been proposed for the purpose of improving the mold releasability, rigidity, one-dimensional stability, etc. of the resin (Japanese Patent Publication No. 35929/1983). However, molded products obtained using this composition have a lot of floating glass fibers, and a new problem arises in that a product with a good appearance cannot be obtained.

[課題を解決するための手段] 本発明者らは上記課題を解決するため鋭意研究を行なっ
たところ、ガラス繊維強化ポリカーボネートに配合する
オルガノポリシロキサンの量を調整することにより、外
観を損わずに離型性が改良できることを見い出し、ここ
に発明を完成した。
[Means for Solving the Problems] The present inventors conducted intensive research to solve the above problems, and found that by adjusting the amount of organopolysiloxane blended into glass fiber reinforced polycarbonate, it was possible to avoid deteriorating the appearance. They discovered that the mold releasability could be improved and completed the invention.

すなわち本発明は、(a)ポリカーボネート樹脂50〜
97重量%、(b)ガラス繊維3〜50重量%および(
c)オルガノポリシロキサン0.05〜0.4重量%か
らなるポリカーボネート樹脂組成物を提供するものであ
る。
That is, the present invention provides (a) polycarbonate resin 50 to
97% by weight, (b) 3-50% by weight of glass fibers and (
c) A polycarbonate resin composition comprising 0.05 to 0.4% by weight of organopolysiloxane is provided.

本発明で用いる(a)ポリカーボネート樹脂は溶剤法、
すなわち塩化メチレン等の溶剤中で公知の酸受溶体9分
子量調整剤の存在下、二価フェノールとホスゲンのよう
なカーボネート前駆体との反応または二価フェノールと
ジフェニルカーボネートのようなカーボネート前駆体と
のエステル交換反応によって製造することができる。
(a) The polycarbonate resin used in the present invention is prepared by a solvent method,
That is, the reaction of a dihydric phenol with a carbonate precursor such as phosgene or the reaction of a dihydric phenol with a carbonate precursor such as diphenyl carbonate in the presence of a known acid acceptor 9 molecular weight regulator in a solvent such as methylene chloride. It can be produced by transesterification.

ここで、好適に使用し得る二価フェノールとしてはビス
フェノール類があり、特に2.2−ビス(4−ヒドロキ
シフェニル)プロパン(ビスフェノールA)が好ましい
。また、ビスフェノールAの一部または全部を他の二価
フェノールで置換したものであってもよい。ビスフェノ
ールA以外の二価フェノールとしては、例えばハイドロ
キノン、4.4’−ジヒドロキシジフェニル、ビス(4
−ヒドロキシフェニル)アルカン、ビス(4−ヒドロキ
シフェニル)シクロアルカン、ビス(4−ヒドロキシフ
ェニル)スルフィド、ビス(4−ヒドロキシフェニル)
スルホン、ビス(4−ヒドロキシフェニル)スルホキシ
ド、ビス(4−ヒドロキシフェニル)エーテルのような
化合物またはビス(3,5−ジブロモ−4−ヒドロキシ
フェニル)プロパン、ビス(3,5−ジクロロ−4−ヒ
ドロキシフェニル)プロパンのようなハロゲン化ビスフ
ェノール類をあげることができる。これら二価フェノー
ルは二価フェノールのホモポリマーまたは2種以上のコ
ポリマー若しくはブレンド物であってもよい。
Here, dihydric phenols that can be suitably used include bisphenols, and 2,2-bis(4-hydroxyphenyl)propane (bisphenol A) is particularly preferred. Further, part or all of bisphenol A may be substituted with other dihydric phenol. Examples of dihydric phenols other than bisphenol A include hydroquinone, 4,4'-dihydroxydiphenyl, bis(4
-hydroxyphenyl)alkane, bis(4-hydroxyphenyl)cycloalkane, bis(4-hydroxyphenyl)sulfide, bis(4-hydroxyphenyl)
Compounds such as sulfone, bis(4-hydroxyphenyl) sulfoxide, bis(4-hydroxyphenyl) ether or bis(3,5-dibromo-4-hydroxyphenyl)propane, bis(3,5-dichloro-4-hydroxy Examples include halogenated bisphenols such as phenyl)propane. These dihydric phenols may be homopolymers or copolymers or blends of two or more dihydric phenols.

本発明に用いるポリカーボネート樹脂は、機械的強度お
よび成形性の点からして、その粘度平均分子量は10,
000〜100.Gooのものが好ましく、特に15,
000〜60,000のものが好適である。
In terms of mechanical strength and moldability, the polycarbonate resin used in the present invention has a viscosity average molecular weight of 10,
000-100. Goo's is preferred, especially 15,
000 to 60,000 is suitable.

上記(a)成分であるポリカーボネート樹脂の配合割合
は組成物全量の50〜97重量%、好ましくは60〜9
5重量%である。
The blending ratio of the polycarbonate resin, which is the component (a), is 50 to 97% by weight, preferably 60 to 9% by weight, based on the total amount of the composition.
It is 5% by weight.

次に、本発明で用いる(b)ガラス繊維としては市場で
入手できる通常のガラス繊維を任意に使用できるが、チ
ョツプドストランド、カットファイバー、ミルドファイ
バーが特に好ましい。チョツプドストランドとしてはガ
ラス繊維長が1.5〜6mmで繊維径が6〜20μのも
のが好ましく、カットファイバーやミルドファイバーと
してはガラス繊維長が0.02〜1mmで繊維径は6〜
20μのものが好ましい。これらのガラス繊維は単独で
用いるほか組合せて使用することもできる。さらには、
ポリカーボネート樹脂との親和性を高めるために常法に
よる表面処理が施されているものでもよい。
Next, as the glass fiber (b) used in the present invention, any ordinary glass fiber available on the market can be used, but chopped strands, cut fibers, and milled fibers are particularly preferred. The chopped strand preferably has a glass fiber length of 1.5 to 6 mm and a fiber diameter of 6 to 20 μm, and the cut fiber or milled fiber preferably has a glass fiber length of 0.02 to 1 mm and a fiber diameter of 6 to 20 μm.
Preferably, the thickness is 20μ. These glass fibers can be used alone or in combination. Furthermore,
It may be surface-treated by a conventional method in order to increase its affinity with polycarbonate resin.

これらガラス繊維の配合量は組成物全量の3〜50重量
%であり、好ましくは5〜40重量%である。添加量が
3重量%より少ないと、ガラスm維の補強効果が小さく
、50重量%を超えると、組成物の混練、成形が困難と
なり望ましくない。
The blending amount of these glass fibers is 3 to 50% by weight, preferably 5 to 40% by weight, based on the total amount of the composition. When the amount added is less than 3% by weight, the effect of reinforcing the glass m fibers is small, and when it exceeds 50% by weight, it becomes difficult to knead and mold the composition, which is not desirable.

また、本発明で用いる(c)オルガノポリシロキサンは
25℃での粘度が5〜100 、0OOcStであって
、下記の構造式で表わされるものが好ましい。
The organopolysiloxane (c) used in the present invention preferably has a viscosity of 5 to 100 and 0OOcSt at 25°C and is represented by the following structural formula.

(式中、Hl、 R2,R3は水素原子、炭素数1〜6
のアルキル基またはフェニル基であり、それぞれ同じで
あっても異なるものであってもよい。また、m、 nは
Oまたは1以上の整数である。)このようなオルガノポ
リシロキサンの単量体としてはジメチルシロキサンやメ
チルフェニルシロキサンが挙げられる。これらオルガノ
ポリシロキサンの配合量は組成物全量の0.05〜0.
4重量%であることが必要である。添加量がO,OS重
量%未満であると、離型性に効果がなく、0.4重量%
を超えると、ガラス繊維の浮きなどが生じて成形品の外
観が不良となる。
(In the formula, Hl, R2, R3 are hydrogen atoms, carbon number 1-6
are an alkyl group or a phenyl group, and may be the same or different. Further, m and n are O or an integer of 1 or more. ) Examples of such organopolysiloxane monomers include dimethylsiloxane and methylphenylsiloxane. The blending amount of these organopolysiloxanes is 0.05 to 0.05% of the total amount of the composition.
It is necessary that the content be 4% by weight. If the amount added is less than 0.4% by weight, there is no effect on mold releasability.
If it exceeds this value, the glass fibers will float and the appearance of the molded product will be poor.

本発明においては通常、上記(a)ポリカーボネート樹
脂50〜97重量%、(b)ガラス繊維3〜50重量%
および(c)オルガノポリシロキサン0.05〜0.4
重量%よりなる組成物を押出機などを用いてベレット化
する。該ペレットは用途等に応じて射出成形などの手段
によって所望の形状に成形される。
In the present invention, the above (a) polycarbonate resin is usually 50 to 97% by weight, and (b) glass fiber is 3 to 50% by weight.
and (c) organopolysiloxane 0.05-0.4
A composition consisting of % by weight is pelletized using an extruder or the like. The pellets are molded into a desired shape by means such as injection molding depending on the intended use.

[実施例コ 次に、本発明を実施例を用いて詳しく説明する。[Example code] Next, the present invention will be explained in detail using examples.

実施例1〜10 第1表に示すように所定量の(a)ポリカーボネート樹
脂、(b)ガラス繊維および(c)ポリシロキサンを配
合し、二軸押出機を用いて300℃でベレット化した。
Examples 1 to 10 As shown in Table 1, predetermined amounts of (a) polycarbonate resin, (b) glass fiber, and (c) polysiloxane were blended and pelletized at 300°C using a twin-screw extruder.

このベレットを用いて300℃で射出成形を行ない、成
形品の離型性および外観を評価したe GA果を第1表
に示す。なお、離型性は成形品を成形機の突出ビンが突
出す時の油圧にて評価した。この場合、油圧が低いぼど
離型性が良いが実用上20kg/cm2以下であれば良
好である。
Injection molding was performed at 300° C. using this pellet, and the mold release properties and appearance of the molded products were evaluated using eGA results, which are shown in Table 1. The mold releasability was evaluated based on the oil pressure when the ejecting bottle of the molding machine ejects the molded product. In this case, the lower the oil pressure, the better the mold releasability, but in practice it is good if it is 20 kg/cm2 or less.

また、成形品の外観は目視により評価したが、その判定
基準は次のとおりである。
In addition, the appearance of the molded product was visually evaluated, and the criteria for evaluation were as follows.

X・・・・・・ガラス繊維浮き大 △・・・・・・     同     中○・・・・・
・     同     小◎・・・・・・    同
    極小比較例1〜2 第1表に示すようにポリシロキサンの配合量を本発明の
範囲外とした他は実施例1〜10と同様にして行なった
。結果を第1表に示す。
X...Large glass fiber float △... Same as medium ○...
・Same Small ◎・・・ Same Very Small Comparative Examples 1 to 2 As shown in Table 1, the procedure was carried out in the same manner as Examples 1 to 10, except that the amount of polysiloxane was outside the range of the present invention. . The results are shown in Table 1.

比較例3〜5 第1表に示すようにポリシロキサンを用いる代わりに天
然パラフィン、ポリエチレンワックスあるいはみつろう
を用いた他は実施例1〜10と同様にして行なった。結
果を第1表に示す。
Comparative Examples 3 to 5 Comparative Examples 1 to 10 were carried out in the same manner as in Examples 1 to 10, except that natural paraffin, polyethylene wax, or beeswax was used instead of polysiloxane as shown in Table 1. The results are shown in Table 1.

/ /′ (注)中1ポリカーボネート(出光石油化学■製)A 
: rA 2.500J 、分子量23,000B 、
 rA 2,200J 、分子量21,000C: r
A 2,700J 、分子量27,000中2ガラス繊
維(日本電気硝子■製) D;チョツプドストランド 繊維長3mm、径13μ E:ミルドファイバー 平均繊維長0.04mm、径9μ *3ポリシロキサン(トーレシリコーン■製)F ; 
rSH200J  (ジメチルシロキサンを主成分とす
るもの) a 、  rsH550J  (メチルフェニルシロキ
サンを主成分とするもの) 中4天然パラフィン;日木精蝋■製、’5PO145゜
中5ポリエチレンワックス;三井石油化学工業■製、「
ハイワックス400」 *6みつろう;三木化学■製、「ゴールデンブランド」 [発明の効果コ 本発明によれば成形品の外観を損わないで、しかも離型
性に優れたガラス繊維強化ポリカーボネート組成物を得
ることができる。
/ /' (Note) Medium 1 polycarbonate (manufactured by Idemitsu Petrochemical ■) A
: rA 2.500J, molecular weight 23,000B,
rA 2,200J, molecular weight 21,000C: r
A 2,700J, molecular weight 27,000 in 2 glass fiber (manufactured by Nippon Electric Glass ■) D: Chopped strand fiber length 3mm, diameter 13μ E: Milled fiber average fiber length 0.04mm, diameter 9μ *3 Polysiloxane ( Made by Toray Silicone ■) F;
rSH200J (Main component is dimethylsiloxane) a, rsH550J (Main component is methylphenylsiloxane) Medium 4 natural paraffin; manufactured by Hiki Seiro ■, '5PO145゜ Medium 5 polyethylene wax; Mitsui Petrochemical Industries ■ Manufactured by “
Hiwax 400" *6 Beeswax; manufactured by Miki Kagaku ■, "Golden Brand" [Effects of the invention: According to the present invention, a glass fiber-reinforced polycarbonate composition that does not impair the appearance of molded products and has excellent mold releasability. can be obtained.

従って、従来困難であった複雑形状で外観に優れた成形
品を得ることができる。それ故、本発明の組成物はOA
機器等の各種電気・電子部品などの製造に有用である。
Therefore, it is possible to obtain a molded product with a complex shape and excellent appearance, which has been difficult to achieve in the past. Therefore, the composition of the present invention
It is useful for manufacturing various electrical and electronic parts such as equipment.

特許出願人  出光石油化学株式会社Patent applicant: Idemitsu Petrochemical Co., Ltd.

Claims (1)

【特許請求の範囲】 (a)ポリカーボネート樹脂50〜97重量%、 (b)ガラス繊維3〜50重量%および (c)オルガノポリシロキサン0.05〜0.4重量%
からなるポリカーボネート樹脂組成物。
Scope of Claims: (a) 50-97% by weight of polycarbonate resin, (b) 3-50% by weight of glass fiber, and (c) 0.05-0.4% by weight of organopolysiloxane.
A polycarbonate resin composition consisting of:
JP63073148A 1988-03-29 1988-03-29 Polycarbonate resin composition Expired - Lifetime JPH0733474B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP63073148A JPH0733474B2 (en) 1988-03-29 1988-03-29 Polycarbonate resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP63073148A JPH0733474B2 (en) 1988-03-29 1988-03-29 Polycarbonate resin composition

Publications (2)

Publication Number Publication Date
JPH01247456A true JPH01247456A (en) 1989-10-03
JPH0733474B2 JPH0733474B2 (en) 1995-04-12

Family

ID=13509819

Family Applications (1)

Application Number Title Priority Date Filing Date
JP63073148A Expired - Lifetime JPH0733474B2 (en) 1988-03-29 1988-03-29 Polycarbonate resin composition

Country Status (1)

Country Link
JP (1) JPH0733474B2 (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6451906B1 (en) 1999-11-26 2002-09-17 General Electric Company Flame-retardant resin composition and molded article consisting of the same
US6727303B2 (en) 2001-08-30 2004-04-27 Teijin Chemicals, Ltd. Flame retardant aromatic polycarbonate resin composition and molded articles thereof
JP2005095109A (en) * 2003-09-26 2005-04-14 Kirin Brewery Co Ltd Manufacturing method of fermented malt beverage
JP2011252061A (en) * 2010-06-01 2011-12-15 Asahi Kasei Chemicals Corp Detergent

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5155399A (en) * 1974-09-16 1976-05-15 Gen Electric ORUGANOHORISHIROKISAN
JPS5935929A (en) * 1982-08-23 1984-02-27 Yokohama Rubber Co Ltd:The Tire forming drum

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5155399A (en) * 1974-09-16 1976-05-15 Gen Electric ORUGANOHORISHIROKISAN
JPS5935929A (en) * 1982-08-23 1984-02-27 Yokohama Rubber Co Ltd:The Tire forming drum

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6451906B1 (en) 1999-11-26 2002-09-17 General Electric Company Flame-retardant resin composition and molded article consisting of the same
US6727303B2 (en) 2001-08-30 2004-04-27 Teijin Chemicals, Ltd. Flame retardant aromatic polycarbonate resin composition and molded articles thereof
JP2005095109A (en) * 2003-09-26 2005-04-14 Kirin Brewery Co Ltd Manufacturing method of fermented malt beverage
JP2011252061A (en) * 2010-06-01 2011-12-15 Asahi Kasei Chemicals Corp Detergent

Also Published As

Publication number Publication date
JPH0733474B2 (en) 1995-04-12

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