JPS61254662A - Resin composition - Google Patents

Resin composition

Info

Publication number
JPS61254662A
JPS61254662A JP9650185A JP9650185A JPS61254662A JP S61254662 A JPS61254662 A JP S61254662A JP 9650185 A JP9650185 A JP 9650185A JP 9650185 A JP9650185 A JP 9650185A JP S61254662 A JPS61254662 A JP S61254662A
Authority
JP
Japan
Prior art keywords
component
volume
40vol
length
aromatic polyamide
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.)
Pending
Application number
JP9650185A
Other languages
Japanese (ja)
Inventor
Mitsuo Higashiya
東谷 光男
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.)
Seiko Epson Corp
Original Assignee
Seiko Epson Corp
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 Seiko Epson Corp filed Critical Seiko Epson Corp
Priority to JP9650185A priority Critical patent/JPS61254662A/en
Publication of JPS61254662A publication Critical patent/JPS61254662A/en
Pending legal-status Critical Current

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  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PURPOSE:A resin composition suitable for small-sized electronic devices, etc., capable of being made lighter and smaller, having improved reinforcement, dimensional stability and molding properties, obtained by blending aromatic polyamide resin with specific amounts of carbon fibers, glass fibers, etc. CONSTITUTION:(A) 40-80vol% aromatic polyamide resin is blended with (B) 0.1-40vol% carbon fibers having 0.5-0.01m/m length, (C) 0.1-40vol% glass fibers having 0.5-0.01m/m length, (D) 0.1-40vol% inorganic needle-like crystal (e.g., whisker of potassium titanate or silicon carbide) and, (E) 0.01-5vol% zinc stearate. A preferable blending ratio of the components is 55-70vol% component A, 10-30vol% component B, 10-30vol% component C, 5-10vol% component D, and 0.1-1.0vol% component E.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、精密金属部品の代替となる熱可塑性4kj 
119 M+ d?:Ah tr 14M−?ス〔発明
の概要〕 本発明は、小型電子機器、磁気・光メモリー機器、ハン
ディ−型情報機器分野において、芳香族ポリアミド樹脂
に炭素繊維・ガラス繊維・無機系針状結晶体・ステアリ
ン酸亜鉛を複合化し、成形することで、補強・寸法安定
性・成形性が向上し、軽量小型化が可能となる。
[Detailed Description of the Invention] [Industrial Application Field] The present invention provides a thermoplastic 4kj material that can replace precision metal parts.
119 M+ d? :Ah tr 14M-? [Summary of the Invention] The present invention is useful in the fields of small electronic devices, magnetic/optical memory devices, and handheld information devices, in which carbon fibers, glass fibers, inorganic acicular crystals, and zinc stearate are added to aromatic polyamide resin. Composite and molding improves reinforcement, dimensional stability, and moldability, making it possible to reduce weight and size.

〔従来技術〕[Prior art]

従来、プロッピーディスクドライブのシャーシの構造材
料は、Atダイキャスト品を切削、研摩を経て利用して
いる。携帯型音響機器は、金属プレス部品をAtシャー
シや他の構成部品と組合せて)実用化している。
Conventionally, the structural material for the chassis of a proppy disk drive is an At die-cast product that has been cut and polished. Portable audio equipment has been put into practical use (by combining metal press parts with At chassis and other components).

〔発明か解決しようとする問題点及び目的〕軽量小型で
生産性の向上が見込める材料として、熱可腰性合成樹脂
の射出成形品が考えられる。
[Problems and objects to be solved by the invention] Injection molded products of thermoplastic synthetic resin are considered as materials that are lightweight and compact and can be expected to improve productivity.

しかし、高強度化9寸法安定性、成形性向上などの惣性
で、実用性が不充分である。
However, its practical properties are insufficient due to its advantages such as high strength, dimensional stability, and improved formability.

適用に供しうる物性としては 比重 K −、,71121,7以下 引張強度 K−71152000以上4f/−曲げ強度
 K−72032500以上Kpflcd曲1f弾性率
1−7205 15XID’以上Kpf/aA 線膨張係数 −2,5X10叫以下 cm 7cm / ”(:。
Physical properties that can be applied include specific gravity K -, 71121.7 or less Tensile strength K-71152000 or more 4f/- Bending strength K-72032500 or more Kpflcd curve 1f Elastic modulus 1-7205 15XID' or more Kpf/aA Linear expansion coefficient -2 , 5X10cm or less cm 7cm/”(:.

成形収縮率 −a2以下% ロックウル硬FRD−785100以上(Mスケール) 流動値(フローテスター)K7210 10以上(−j/5ec) が満たされていることが条件である。Mold shrinkage rate -a2 or less% Rockul hard FRD-785100 or higher (M scale) Flow value (flow tester) K7210 10 or more (-j/5ec) The condition is that the following conditions are met.

本発明の目的は、上記物性項目についてバランス良く適
用し得る樹脂組成物を提案する事にある〔問題点を解決
するための手段〕 本発明の樹脂組成物は、 (1)芳香族ポリアミド樹脂 40〜b(2)炭素線維
(長さ0.5〜0.01%)α1〜40容童第 (8) カ5 ス繊維(長さ0. 5〜Q、o 1% 
)(L1〜401〜4 0容量無m系針状結晶体 [L1〜401〜40容量ス
テアリン酸亜鉛 α01〜5容f%の組成であることを
特徴とする。
The purpose of the present invention is to propose a resin composition that can be applied in a well-balanced manner with respect to the above-mentioned physical properties [Means for solving the problems] The resin composition of the present invention includes: (1) aromatic polyamide resin 40 - b (2) Carbon fiber (length 0.5-0.01%) α1-40 Yododai (8) Cass fiber (length 0.5-Q, o 1%
) (L1-401-40 volumeless m-type acicular crystal body [L1-401-40 volume zinc stearate α01-5 volume f% composition.

〔作用〕[Effect]

本発明の上記組成によれば 比重      (1)と(2) (8) (4)の合
計の比率引張強度    (2) (a) (4)曲げ
強度    (2) (8) (4)曲げ弾性率   
(2) (1) (4)線膨張係数   (2) (3
)(4)成形収縮率   <2) (8)(4)ロック
ウェル硬度(2) (8) 流動値        (6) という相関関係で組成作用が現われる。
According to the above composition of the present invention, specific gravity (1) and (2) (8) (4) total specific tensile strength (2) (a) (4) bending strength (2) (8) (4) bending elasticity rate
(2) (1) (4) Linear expansion coefficient (2) (3
) (4) Molding shrinkage <2) (8) (4) Rockwell hardness (2) (8) Flow value (6) Composition effects appear in the following correlations.

炭素繊維とガラス繊維は長さα5z以上又は(1,01
x以下の場合は、繊維配向性により線膨張係数と成形収
縮率においてバランスのとれた物性が実現できない。
Carbon fibers and glass fibers have a length α5z or more or (1,01
If it is less than x, it is not possible to achieve balanced physical properties in terms of linear expansion coefficient and molding shrinkage rate due to fiber orientation.

〔実施例〕〔Example〕

以下実施例に基づいて説明する。使用する芳香族ポリア
ミド樹脂は、M X D −6(三菱ガス化学社製)で
ある。8o容1%以上の組成では補強効果がうすれ14
0容童%以下では、成形困難となり1曲げ弾性率が低下
する。好ましくは55〜70容ii%が良い。炭素繊維
とガラス繊維はα1容量%以下だと効果が薄く、40容
蓋%以上は成形不可能となる。好ましくは10〜30容
量%が良い。無機系針状結晶体は、チタン酸カリウムウ
ィスカーや炭化ケイ素ウィスカーなどがある。上記の繊
維や針状結晶体は、a、1容社%以下では効果がうすれ
、又40容鷺%をこえると物性が保てず1加工性が悪化
する。好ましくは5〜10容量%が良い。さらにその表
面にはシラン系の表面処理剤をコートするか他にチタン
系なども良好である。ステアリン酸亜鉛は滑剤としての
主効果が考えられるが他にシリコンオイルやステアリン
酸や脂肪ばアミドなど有効である。分量として、[L。
The following will be explained based on examples. The aromatic polyamide resin used is MXD-6 (manufactured by Mitsubishi Gas Chemical Co., Ltd.). The reinforcing effect is weakened when the composition is 1% or more by 8o volume14
If it is less than 0%, molding becomes difficult and the flexural modulus decreases. Preferably it is 55 to 70% by volume. Carbon fibers and glass fibers are less effective when α is less than 1% by volume, and cannot be molded when α is more than 40% by volume. Preferably it is 10 to 30% by volume. Examples of inorganic needle-like crystals include potassium titanate whiskers and silicon carbide whiskers. The above-mentioned fibers and acicular crystals are less effective if the content is less than 1% by volume, and if the content exceeds 40% by volume, the physical properties cannot be maintained and workability deteriorates. Preferably it is 5 to 10% by volume. Furthermore, the surface may be coated with a silane-based surface treatment agent, or a titanium-based surface treatment agent may also be used. Zinc stearate is thought to have a main effect as a lubricant, but other effective agents include silicone oil, stearic acid, and fatty acid amide. As for the quantity, [L.

1容量%以下だと効果はなく、5容it%以上だと流動
性が良すぎて逆に物性を劣化し加工しずらくなる。好ま
しくは(L1〜1.0容量%が良い。混練機は2軸押用
機CPCM−30池貝鉄工所製)を使用したが、バンバ
IJ −ミ午す−でも良い。射出成形機は、I’S−4
01nSA、日清樹脂工業社製を使用し、J工S標準試
験片を成形評価した。その結果を表1に示す。
If it is less than 1% by volume, there will be no effect, and if it is more than 5% by volume, the fluidity will be too good and the physical properties will deteriorate, making it difficult to process. Preferably (L1 to 1.0% by volume is good. The kneader used is a twin-screw presser CPCM-30 manufactured by Ikegai Iron Works), but a Bamba IJ-Migosu- may also be used. The injection molding machine is I'S-4
01nSA, manufactured by Nisshin Jushi Kogyo Co., Ltd., was used to evaluate the molding of J-Ko S standard test pieces. The results are shown in Table 1.

〔発明の効果〕〔Effect of the invention〕

以上、本発明の樹脂組成物は、小型電子機器や情報機器
の構造材料として、高強度・寸法安定性・成形向上・軽
量小型に適した有用な産業材料である。
As described above, the resin composition of the present invention is a useful industrial material suitable for high strength, dimensional stability, improved molding, light weight, and small size as a structural material for small electronic devices and information devices.

Claims (4)

【特許請求の範囲】[Claims] (1)芳香族ポリアミド樹脂 40〜80容量%(1) Aromatic polyamide resin 40-80% by volume (2)炭素繊維(長さ0.5〜0.01m/m)0.1
〜40容量%
(2) Carbon fiber (length 0.5-0.01m/m) 0.1
~40% by volume
(3)ガラス繊維(長さ0.5〜0.01m/m)0.
1〜40容量%
(3) Glass fiber (length 0.5-0.01m/m) 0.
1-40% by volume
(4)無機系針状結晶体 0.1〜40容量%(5)ス
テアリン酸亜鉛 0.01〜5容量%の組成であること
を特徴とする樹脂組成物。
(4) A resin composition having a composition of 0.1 to 40% by volume of inorganic acicular crystals (5) 0.01 to 5% by volume of zinc stearate.
JP9650185A 1985-05-07 1985-05-07 Resin composition Pending JPS61254662A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP9650185A JPS61254662A (en) 1985-05-07 1985-05-07 Resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP9650185A JPS61254662A (en) 1985-05-07 1985-05-07 Resin composition

Publications (1)

Publication Number Publication Date
JPS61254662A true JPS61254662A (en) 1986-11-12

Family

ID=14166850

Family Applications (1)

Application Number Title Priority Date Filing Date
JP9650185A Pending JPS61254662A (en) 1985-05-07 1985-05-07 Resin composition

Country Status (1)

Country Link
JP (1) JPS61254662A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0360611A2 (en) * 1988-09-22 1990-03-28 Mitsui Petrochemical Industries, Ltd. Polyamide resin compositions
JPH02127467A (en) * 1988-11-08 1990-05-16 Asahi Chem Ind Co Ltd Polyamide resin molding material
EP0691996A1 (en) * 1993-03-29 1996-01-17 E.I. Du Pont De Nemours And Company Polyamide resin composition
EP0708142A2 (en) * 1989-08-31 1996-04-24 Mitsui Petrochemical Industries, Ltd. Polyamide resin compositions
JP2011116841A (en) * 2009-12-02 2011-06-16 Toyobo Co Ltd Carbon filament-reinforced polyamide composite material
JP2011132550A (en) * 2011-04-07 2011-07-07 Mitsubishi Engineering Plastics Corp Polyamide resin composition and conductive shaft-like molding

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0360611A2 (en) * 1988-09-22 1990-03-28 Mitsui Petrochemical Industries, Ltd. Polyamide resin compositions
JPH02127467A (en) * 1988-11-08 1990-05-16 Asahi Chem Ind Co Ltd Polyamide resin molding material
EP0708142A2 (en) * 1989-08-31 1996-04-24 Mitsui Petrochemical Industries, Ltd. Polyamide resin compositions
EP0708142A3 (en) * 1989-08-31 1996-06-12 Mitsui Petrochemical Ind Polyamide resin compositions
EP0691996A1 (en) * 1993-03-29 1996-01-17 E.I. Du Pont De Nemours And Company Polyamide resin composition
EP0691996A4 (en) * 1993-03-29 1997-06-18 Du Pont Polyamide resin composition
JP2011116841A (en) * 2009-12-02 2011-06-16 Toyobo Co Ltd Carbon filament-reinforced polyamide composite material
JP2011132550A (en) * 2011-04-07 2011-07-07 Mitsubishi Engineering Plastics Corp Polyamide resin composition and conductive shaft-like molding

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