JPH01230655A - Conductive resin composition - Google Patents
Conductive resin compositionInfo
- Publication number
- JPH01230655A JPH01230655A JP5708388A JP5708388A JPH01230655A JP H01230655 A JPH01230655 A JP H01230655A JP 5708388 A JP5708388 A JP 5708388A JP 5708388 A JP5708388 A JP 5708388A JP H01230655 A JPH01230655 A JP H01230655A
- Authority
- JP
- Japan
- Prior art keywords
- weight
- resin composition
- carbon black
- parts
- resin
- 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.)
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- Compositions Of Macromolecular Compounds (AREA)
- Conductive Materials (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明は導電性樹脂組成物に関するものであり、より詳
しくはカーボンブラックを使用してなる低粘度を有する
導電性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 conductive resin composition, and more particularly to a conductive resin composition having a low viscosity and using carbon black. .
(従来の技術)
一般に、カーボンブラックを導電材として使用した導電
性樹脂組成物は知られている。そして所望の導電性を得
るためにはカーボンブラックの配合量を増量すれば可能
となるが、カーボンブラックをあまり大量に配合すると
樹脂組成物としての軟化流動性が低下し、成形が困難に
なるとともに得られた成形物が脆くなる。(Prior Art) Generally, conductive resin compositions using carbon black as a conductive material are known. In order to obtain the desired conductivity, it is possible to increase the amount of carbon black blended, but if too much carbon black is blended, the softening fluidity of the resin composition will decrease, making molding difficult. The resulting molded product becomes brittle.
そこで、従来ではカーボンブラックの改質や界面活性剤
の添加等の手法によシ対処してきた。Conventionally, methods such as modifying carbon black and adding surfactants have been used to deal with this problem.
(発明が解決しようとする問題点)
しかしながら、これら従来の方法では、所望の粘度を得
るには導電性を犠牲にしなければならないという問題点
があり、また一方コスト面からはやはυ導電グ材として
はカーボンブラックを使用するのが好ましいことからカ
ーボンブラックを用いた導電性と粘度とのバランスのよ
い樹脂組成物が望まれていた。(Problems to be Solved by the Invention) However, in these conventional methods, there is a problem in that conductivity must be sacrificed in order to obtain the desired viscosity. Since it is preferable to use carbon black as the material, a resin composition using carbon black with a good balance between conductivity and viscosity has been desired.
(問題点を解決するだめの手段)
そこで、本発明者等はこれらの問題点を解決すべく鋭意
検討した結果、樹脂にゴム成分を添加することによりカ
ーボンブラックの配合iを低下できると同時に得られる
樹脂組成物に柔軟性を付与でき、また特定量のミネラル
オイルを添加することにより樹脂組成物の粘度と最適化
できることを見い出し本発明を完成するに至った。(Means to Solve the Problems) Therefore, as a result of intensive studies to solve these problems, the inventors of the present invention found that by adding a rubber component to the resin, it was possible to reduce the blend i of carbon black and at the same time obtain an advantage. The present inventors have discovered that flexibility can be imparted to a resin composition, and that the viscosity of the resin composition can be optimized by adding a specific amount of mineral oil, and the present invention has been completed.
すなわち、本発明の目的は高い導電性を示し、かつ種々
成形するのに好適な程度の粘度を有する、導電性と粘度
とのバランスの優れた導電性樹脂組成物を提供するもの
である。That is, an object of the present invention is to provide a conductive resin composition that exhibits high conductivity, has a viscosity suitable for various moldings, and has an excellent balance between conductivity and viscosity.
そして、かかる目的はポリスチレン系樹脂中のポリスチ
レン成分100重量部に、ミネラルオイル/〜/夕重量
部、ブタジエンゴム1〜10重量部、及びDBP吸油量
ioomtiiooy以上のカーボンブラック70〜2
0重量部を配合してなる体積固有抵抗値が/ X /
010Ω・α以下かつメルトインデックスフローが!;
g/10分以上であることを特徴とする導電性樹脂組成
物により容易に達成される。This purpose is to add 100 parts by weight of the polystyrene component in the polystyrene resin, 1 to 10 parts by weight of mineral oil, 1 to 10 parts by weight of butadiene rubber, and 70 to 2 parts of carbon black with a DBP oil absorption of ioomtiiooy or more.
The volume resistivity value obtained by blending 0 parts by weight is /
010Ω・α or less and melt index flow! ;
This can be easily achieved by using a conductive resin composition characterized in that it has a conductive resin composition of at least g/10 minutes.
仝冗門は、刀−ホーンフッツクに得電グとし、主に、カ
ーボンブラックとゴムとミネラルオイルから構成される
ポリスチレン系樹脂において、体積固有抵抗値が/ 0
”Ω・α以下でかつ、軟化流導電性樹脂である。This is a polystyrene resin mainly composed of carbon black, rubber, and mineral oil, which has a volume resistivity of / 0.
”It is less than Ω・α and is a softening flow conductive resin.
本発明で用いるポリスチレン系樹脂としては、特に限定
されるものではないが、例えば三菱モンサント化成■製
“ダイヤレックス”HT−gg。The polystyrene resin used in the present invention is not particularly limited, but for example, "Dialex" HT-gg manufactured by Mitsubishi Monsanto Chemicals.
HT−7A 、YH−9!;/、旭化成工業■製−8t
yron ”I10’l 、 ll0g 、 II9コ
等が挙げられる。HT-7A, YH-9! ;/, Asahi Kasei Kogyo ■-8t
Examples include yron"I10'l, ll0g, II9ko, etc.
またミネラルオイルとしては食品添加用に使用できるも
のがよく、例えば松材石油研究所製“RAMBUS M
−26o”が挙げられ、特に2S℃での粘度が/ 00
−II 00 cpsのものが樹脂との混練性や混線後
の流動性の向上の点から好ましい。In addition, mineral oils that can be used as food additives are good, such as "RAMBUS M" manufactured by Matsuzai Oil Research Institute.
-26o'', especially when the viscosity at 2S℃ is /00
-II 00 cps is preferable from the viewpoint of kneading with the resin and improving fluidity after mixing.
ブタジェンゴムとしては、特に限定されるものではない
が、好ましくはブタジェン含有量がよ0チ以上のもの、
好ましくはgo%以上のもの、例えば旭化成工業■製“
タフブレンA″、”タフプレン−〇’12″を用いると
導電性及び柔軟性付与の点で好ましい。The butadiene rubber is not particularly limited, but preferably has a butadiene content of 0% or more,
Preferably more than go%, for example, manufactured by Asahi Kasei Corporation.
It is preferable to use Toughprene A" and "Toughprene-0'12" from the viewpoint of imparting conductivity and flexibility.
カーボンブラックとしては導電性付与剤として通常用い
られるものであって、例えばDBP吸油量がioomt
/ioog以上、好ましくは/jtO〜!l00d!/
/θO1のものを用いるのがよい。この様なカーボンブ
ラックとしては例えば三菱化成工業■製″430!;O
E3”、−*3isoB”、≠3’1SOE3゜豐39
!;OB、日本イージー■製1ケッチエンブラックEC
″、“DJ−600″、東海カーボン社製≠ysoo
、≠5500並びに電気化学工業■製アセチレンブラッ
ク等が挙げられる。Carbon black is commonly used as a conductivity imparting agent, and for example, DBP oil absorption is ioomt.
/ioog or more, preferably /jtO~! l00d! /
/θO1 is preferably used. Examples of such carbon black include "430!;O" manufactured by Mitsubishi Chemical Corporation.
E3", -*3isoB", ≠3'1SOE3゜豐39
! ;OB, Japan Easy ■ 1 Ketch Enblack EC
”, “DJ-600”, manufactured by Tokai Carbon Co., Ltd.≠ysoo
, ≠5500, and acetylene black manufactured by Denki Kagaku Kogyo ■.
本発明の樹脂組成物はこれらの成分を均一に混練したも
のであって、その配合割合としてはポリスチレン系樹脂
中のポリスチレン成分10゜重量部に対し、カーボンブ
ラックを通常70〜コO重量部、好ましくは10〜75
重量部、ブタジェンゴムを通常2〜70重量部、好まし
くは5−8重量部、ミネラルオイルを通常1〜15重量
部、好ましくは2〜10重量部とすればよい0
本発明の樹脂組成物を製造するための混練には、これら
を適当な割合で配合し、”ヘンシルミキサー″ や適当
な混合機を用いてプレ混合した後、/30−250℃に
加熱して熔融させた状態で、ミキシングロール、バンバ
リーミキサ−1−軸または二軸のエキストルーダ−やブ
スコニーダー等を用いて行われる。The resin composition of the present invention is made by uniformly kneading these components, and the blending ratio is usually 70 to 70 parts by weight of carbon black to 10 parts by weight of the polystyrene component in the polystyrene resin. Preferably 10-75
Parts by weight, butadiene rubber is usually 2 to 70 parts by weight, preferably 5 to 8 parts by weight, and mineral oil is usually 1 to 15 parts by weight, preferably 2 to 10 parts by weight. Manufacturing the resin composition of the present invention For kneading, mix these in appropriate proportions, pre-mix using a "Henshil mixer" or an appropriate mixer, and then heat to 30-250°C to melt and mix. This is carried out using a roll, a Banbury mixer, a single-screw or twin-screw extruder, a Busco kneader, or the like.
このようにして得られた本発明の樹脂組成物は体積固有
抵抗値が7×1010Ω・α以下、好ましくは/x10
8Ω・α以下でありかつメルトインデックスフロー(M
I )が31/10分以上、好ましくは19710分以
上の導電性と粘度とのバランスがよい導電性樹脂組成物
である。The resin composition of the present invention thus obtained has a volume resistivity value of 7×10 10 Ω·α or less, preferably /×10
8Ω・α or less and melt index flow (M
The conductive resin composition has a good balance between conductivity and viscosity, with I) of 31/10 minutes or more, preferably 19710 minutes or more.
(実施例)
次に、本発明を実施例により更に詳細に説明するが本発
明はその要旨をこえない限り以下の実施例に限定される
ものではない。(Examples) Next, the present invention will be explained in more detail with reference to Examples, but the present invention is not limited to the following Examples unless the gist thereof is exceeded.
比較例/〜7および実施例/〜// 表−7に比較例と実施例を示した。Comparative Example/~7 and Example/~// Table 7 shows comparative examples and examples.
ポリスチレン樹脂(三菱モンサント化成■製う°イヤレ
ックス″YH−15/)にブタジエ/ゴAJ、ミネラル
オイル並びにカーボンブラック(下記光−2)を配合し
、これを測定ヘッドにミキサーを取付けた■東洋精機製
作新製“ラボ・プラストミル”を用いて760℃で混練
した。Polystyrene resin (Mitsubishi Monsanto Kasei's "Yarex" YH-15/) was blended with Butadier/Go AJ, mineral oil, and carbon black (Hikari-2 below), and a mixer was attached to the measuring head. The mixture was kneaded at 760° C. using a new “Labo Plastomill” manufactured by Seiki Seiki.
混練後、得られた樹脂組成物をiso〜/AO℃のqイ
ンチ加熱型コ本ロールでシート状組成物を得、これを/
40〜7gO℃、/ 50−200Ki/cm2の加熱
プレスで厚さ2mm、−辺70−の正方形の平板に成形
した。After kneading, the obtained resin composition was heated with a q-inch heating type roll at iso to /AO°C to obtain a sheet-like composition, and this was
It was molded into a square flat plate with a thickness of 2 mm and a side of 70 by a hot press at 40 to 7 gO<0>C and 50 to 200 Ki/cm2.
成形板は幅2crn1長さiocmにダイヤモンドカッ
ターで切り出した試験片に、電極間隔が7のになるよう
に電極を取り付けて、体積固有抵抗を測定した。The molded plate was a test piece cut out with a diamond cutter to have a width of 2 crn and a length of iocm, and electrodes were attached to the molded plate so that the electrode spacing was 7, and the volume resistivity was measured.
なお、組成物の体積固有抵抗は試料抵抗が/ o6〜1
016Ωの範囲にあるときは抵抗計HIGHRESIS
TANCE METERtI32qA (横河・ヒュ
レット・パラカード■製)を用い、また、試料の抵抗が
10’Ω以下のときは、抵抗計” DEG I TAL
MULTMETERTR−A g !; l、″(タケ
ダ理研■製)を用いて、温度25℃、湿度60%の雰囲
気で試験片の抵抗を測定した。In addition, the volume resistivity of the composition is such that the sample resistance is /o6~1
When it is in the range of 0.016Ω, the resistance meter is HIGHRESIST.
Use a TANCE METER tI32qA (manufactured by Yokogawa Hulett Paracard ■), and when the resistance of the sample is 10'Ω or less, use a resistance meter "DEG I TAL".
MULTMETERTR-A g! The resistance of the test piece was measured in an atmosphere with a temperature of 25° C. and a humidity of 60% using a test piece “1” (manufactured by Takeda Riken ■).
S:抵抗測定電極の面積(cm2)
t:電極間の距離(、)
メルトインデックス(MI値)は、前記試験片の残りの
一部を粉砕機により直径0.!rrras以下の粒状体
に粉砕し、これを試料としてMl値測定機、メルトイン
デクサ−MX / 0 /型(全工業■製)を用いて測
定した。S: Area of resistance measuring electrode (cm2) t: Distance between electrodes (,) Melt index (MI value) is determined by grinding the remaining part of the test piece into a pulverizer with a diameter of 0. ! The powder was ground into granules having a size of less than 100 ml, and this was used as a sample to measure the Ml value using a Melt Indexer MX/0/type (manufactured by Zen Kogyo ■).
粉砕した試料を220℃、!;、gKyの荷重をかけ、
内径コ■のノズルから所定時間排出される樹脂重量を測
定し、これを10分間に排出される樹脂の重量に換算し
てMI値とした。The crushed sample was heated to 220℃! ;, Apply a load of gKy,
The weight of the resin discharged for a predetermined period of time from the nozzle with the inner diameter C was measured, and this was converted to the weight of the resin discharged in 10 minutes, which was defined as the MI value.
プ!ジエンゴム、ミネラルオイル並びにカーボンブラッ
クの配合重量部はポリスチレン系樹脂中のポリスチレン
成分100重量部に対するものである。P! The weight parts of the diene rubber, mineral oil, and carbon black are based on 100 parts by weight of the polystyrene component in the polystyrene resin.
ポリスチレン系樹脂並びにブタジェンゴム中のスチレン
成分量とブタジェン成分量は適当量の樹脂又はゴムを重
水素化クロロポルムで溶解し、’H−NMR分析装置で
スチレン成分については共鳴周波数が6.5〜?、/p
pm、ブタジェン成分については!、41ppm位置で
の強度比から分子量換算して、重量比を求めた。The amount of styrene component and butadiene component in polystyrene resin and butadiene rubber can be determined by dissolving an appropriate amount of resin or rubber with deuterated chloroporm, and using an 'H-NMR analyzer to determine the resonance frequency of the styrene component from 6.5 to ? ,/p
Regarding pm and butadiene ingredients! , the weight ratio was determined by converting the intensity ratio at the 41 ppm position into molecular weight.
ポリスチレン系樹脂中のミネラルオイル量はメタノール
で抽出後、薄層クロマトグラフィーで分離した。成分を
赤外線吸収スペクトル分析で確認してから、分離収集し
、重量法で求めた。The amount of mineral oil in the polystyrene resin was extracted with methanol and then separated using thin layer chromatography. The components were confirmed by infrared absorption spectroscopy, separated and collected, and determined by gravimetric method.
(発明の効果)
本発明により高い導電性を示し、かつ種々成形するのに
好適な程度の粘度を有する、導電性と粘度のバランスの
優れた導電性樹脂組成物を得ることができる。(Effects of the Invention) According to the present invention, it is possible to obtain a conductive resin composition that exhibits high conductivity, has a viscosity suitable for various moldings, and has an excellent balance between conductivity and viscosity.
出 願 人 三菱化成工業株式会社 代 理 人 弁理士長谷用 − ほか/名Sender: Mitsubishi Chemical Industries, Ltd. Representative Patent Attorney Hase - Others/names
Claims (1)
重量部に、ミネラルオイル1〜15重量部、ブタジエン
ゴム1〜10重量部、及びDBP吸油量100ml/1
00g以上のカーボンブラック10〜20重量部を配合
してなる体積固有抵抗値が1×10^1^0Ω・cm以
下かつメルトインデックスフローが5g/10分以上で
あることを特徴とする導電性樹脂組成物。(1) Polystyrene component 100 in polystyrene resin
Parts by weight include 1 to 15 parts by weight of mineral oil, 1 to 10 parts by weight of butadiene rubber, and 100 ml/1 DBP oil absorption.
A conductive resin containing 10 to 20 parts by weight of carbon black of 0.00 g or more and having a volume resistivity of 1×10^1^0 Ω・cm or less and a melt index flow of 5 g/10 min or more. Composition.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63057083A JP2642944B2 (en) | 1988-03-10 | 1988-03-10 | Conductive resin composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63057083A JP2642944B2 (en) | 1988-03-10 | 1988-03-10 | Conductive resin composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH01230655A true JPH01230655A (en) | 1989-09-14 |
| JP2642944B2 JP2642944B2 (en) | 1997-08-20 |
Family
ID=13045591
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP63057083A Expired - Lifetime JP2642944B2 (en) | 1988-03-10 | 1988-03-10 | Conductive resin composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2642944B2 (en) |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5221013A (en) * | 1975-08-11 | 1977-02-17 | Tanto Kk | Manufacture of paper pasted tile units |
| JPS5282942A (en) * | 1975-12-29 | 1977-07-11 | Toray Ind Inc | Thermoplastic composite materials |
| JPS54152580A (en) * | 1978-05-22 | 1979-11-30 | Dainippon Ink & Chemicals | Composite resin material |
| JPS61185550A (en) * | 1985-02-13 | 1986-08-19 | Denki Kagaku Kogyo Kk | Styrene resin composition |
-
1988
- 1988-03-10 JP JP63057083A patent/JP2642944B2/en not_active Expired - Lifetime
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5221013A (en) * | 1975-08-11 | 1977-02-17 | Tanto Kk | Manufacture of paper pasted tile units |
| JPS5282942A (en) * | 1975-12-29 | 1977-07-11 | Toray Ind Inc | Thermoplastic composite materials |
| JPS54152580A (en) * | 1978-05-22 | 1979-11-30 | Dainippon Ink & Chemicals | Composite resin material |
| JPS61185550A (en) * | 1985-02-13 | 1986-08-19 | Denki Kagaku Kogyo Kk | Styrene resin composition |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2642944B2 (en) | 1997-08-20 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EXPY | Cancellation because of completion of term |