JPS6312663A - Colorable electrically conductive resin composition - Google Patents

Colorable electrically conductive resin composition

Info

Publication number
JPS6312663A
JPS6312663A JP15511186A JP15511186A JPS6312663A JP S6312663 A JPS6312663 A JP S6312663A JP 15511186 A JP15511186 A JP 15511186A JP 15511186 A JP15511186 A JP 15511186A JP S6312663 A JPS6312663 A JP S6312663A
Authority
JP
Japan
Prior art keywords
parts
weight
fiber
electrically conductive
resin composition
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
JP15511186A
Other languages
Japanese (ja)
Inventor
Eiji Saito
斉藤 栄二
Kazufumi Sakai
酒井 和文
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.)
Tokyo Printing Ink Mfg Co Ltd
Original Assignee
Tokyo Printing Ink Mfg 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 Tokyo Printing Ink Mfg Co Ltd filed Critical Tokyo Printing Ink Mfg Co Ltd
Priority to JP15511186A priority Critical patent/JPS6312663A/en
Publication of JPS6312663A publication Critical patent/JPS6312663A/en
Pending legal-status Critical Current

Links

Landscapes

  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PURPOSE:To obtain the titled composition colorable to desired color, having excellent antistatic effect and suitable for antistatic part such as magazine for IC, etc., by compounding electrically conductive fiber and expanded graphite to a base resin at specific ratios. CONSTITUTION:100pts.(wt.) of a thermoplastic resin (e.g. polyethylene, polypropylene, etc.) is compounded with (A) 1-20pts. of electrically conductive fiber (e.g. metallic fiber, carbon fiber, etc.) having a fiber diameter of 3-20mum and a fiber length of about 1-15mm and (B) 5-30pts. of expanded graphite having a bulk density of <=0.2g/cc, preferably 0.1-0.005g/cc.

Description

【発明の詳細な説明】 本発明は、希望する色調に着色可能であり、帯電防止効
果に優れた着色可能な導電性樹脂組成物に関するもので
ある。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a colorable conductive resin composition that can be colored to a desired color tone and has an excellent antistatic effect.

従来より帯電防止効果の優れた導電性樹脂は、ICやL
SI等保護のためのキャリヤケースや電子部品の包装材
料等に使用されている。
Conventionally, conductive resins with excellent antistatic effects are used for IC and L
It is used in carrier cases to protect SI, etc., and packaging materials for electronic components.

そして、この際に使用する導電性樹脂としては、価格、
機械的な物性のバランス、成形性等の問題上等から、カ
ーボンブラックを樹脂に配合したものが殆んどである。
The conductive resin used in this case has a price,
Most resins are blended with carbon black due to issues such as the balance of mechanical properties and moldability.

しかし、樹脂にカーボンブラックを配合したものは、電
気導電性は良好であるが、得られる成形品の色調が黒色
となり、色別を求められる場合の導電性材料として不適
当であり、美観を求められる様な部分に使用できないの
が現状である。
However, although resin containing carbon black has good electrical conductivity, the resulting molded product has a black tone, making it unsuitable as a conductive material when different colors are required; The current situation is that it cannot be used in areas where it may be exposed.

このため近年、希望する色調に着色可能な感電性樹脂の
開発が試みられている0例えば、樹脂に炭素繊維や金属
繊維等導電性繊維を配合したものは、色調が淡色であり
、このため着色剤の添加で希望する色調の成形品が得ら
れる。
For this reason, in recent years, attempts have been made to develop electrosensitive resins that can be colored to a desired color tone. By adding the agent, a molded product with the desired color tone can be obtained.

しかし、導電性繊維は樹脂との混合の際に、繊維が、樹
脂の流れ方向と平行に配向し易く、得られる成形品の表
面に部分的であるが、非電導性の樹脂層を生じることが
、しばしばあり、このため成形品の全体に優れた帯電防
止効果を得るために導電性繊維を多量に配合しなければ
ならず、感電性樹脂の物性(例えば、耐衝撃性、成形性
等)を著しく低下して好ましくない。
However, when conductive fibers are mixed with resin, the fibers tend to be oriented parallel to the flow direction of the resin, resulting in the formation of a non-conductive resin layer, albeit partially, on the surface of the resulting molded product. However, in order to obtain an excellent antistatic effect throughout the molded product, a large amount of conductive fiber must be blended, and the physical properties of the electrosensitive resin (e.g. impact resistance, moldability, etc.) This is undesirable as it significantly reduces the

本発明者らは、上述のような欠点を解決するため、鋭意
努力した結果導電性繊維を配合する際に膨張黒鉛を添加
すると、導電性繊維の使用が少量であっても、良好な帯
電防止効果が得られ、しかも、着色剤の添加で希望する
色調に容易に着色可能な導電性樹脂組成物が得られるこ
とを知見し、本発明を完成したのである。
In order to solve the above-mentioned drawbacks, the present inventors have made extensive efforts and found that by adding expanded graphite when blending conductive fibers, good antistatic properties can be achieved even when using a small amount of conductive fibers. The present invention was completed based on the finding that a conductive resin composition that is effective and that can be easily colored into a desired color tone by adding a colorant can be obtained.

本発明で使用する膨張黒鉛は粉体であり、嵩密度0.2
g/cc以下のものが適当であり、好ましくは0.1〜
0.005g/ccのものである。粉体の嵩密度が0.
2g/ccをこえるとフィラーとしての樹脂に充填量を
増さなければならない。
The expanded graphite used in the present invention is a powder with a bulk density of 0.2
g/cc or less is appropriate, preferably 0.1~
It is 0.005g/cc. The bulk density of the powder is 0.
If it exceeds 2 g/cc, the amount of resin used as a filler must be increased.

又、嵩密度が余りに小さい場合には取り扱いが困難とな
り樹脂への均一な分散が難しくなる。
Furthermore, if the bulk density is too low, handling becomes difficult and uniform dispersion in the resin becomes difficult.

尚、膨張黒鉛の製造は、公知の方法によればよく、特に
その製造法を限定するものではない。
The expanded graphite may be manufactured by any known method, and the manufacturing method is not particularly limited.

例えば、六員環重合体層が層状に重なり合った炭素の六
方晶系結晶体である黒鉛に、硫酸、アルカリ金属、ハロ
ゲン化合物などを反応させることにより、層と層とを硫
酸根、アルカリ金属、ハロゲン等により結合した黒鉛層
間化合物を形成し、これを100℃以上、好ましくは5
00℃以上の温度で熱処理することにより、外径寸法で
C軸方向が10〜300倍程度にまで膨張した膨張黒鉛
が得られる。
For example, by reacting graphite, which is a hexagonal crystal of carbon in which six-membered ring polymer layers are layered, with sulfuric acid, an alkali metal, a halogen compound, etc. A graphite intercalation compound bonded with halogen etc. is formed, and this is heated to 100°C or higher, preferably 5°C
By heat-treating at a temperature of 00° C. or higher, expanded graphite whose outer diameter has expanded by about 10 to 300 times in the C-axis direction can be obtained.

導電性繊維としては、金属繊維、炭素繊維、金属被覆ガ
ラス繊維等が挙げられる。尚、金属繊維としは、鋼、ス
テンレス、黄銅、銅、アルミニウム等の金属又は合金を
溶融紡糸法、伸展法、押出法、ひびり振動切削性等公知
の方法で繊維化したものを使えばよい。
Examples of the conductive fibers include metal fibers, carbon fibers, metal-coated glass fibers, and the like. As the metal fibers, metals or alloys such as steel, stainless steel, brass, copper, aluminum, etc. may be made into fibers by known methods such as melt spinning, stretching, extrusion, crack vibration machinability, etc. .

又、炭素繊維としては、ポリアクリロニトリル系の炭素
繊維が好ましい。
Further, as the carbon fiber, polyacrylonitrile carbon fiber is preferable.

これら導電性繊維は、繊維径3〜20μ−程度、織組の
長さが1〜15鶴程度のものを使用するとよい。
These conductive fibers preferably have a fiber diameter of about 3 to 20 μm and a weave length of about 1 to 15 strands.

本発明で使用する樹脂としては、ポリエチレン、ポリプ
ロピレン、ポリスチレン、AS樹脂、ABS樹脂、ポリ
アセタール、ポリカーボネート、ポリアミド、ポリエス
テル、ポリ塩化ビニル等熱可塑性樹脂である。
The resin used in the present invention includes thermoplastic resins such as polyethylene, polypropylene, polystyrene, AS resin, ABS resin, polyacetal, polycarbonate, polyamide, polyester, and polyvinyl chloride.

そして配合量は、樹脂100重量部に対して、導電性繊
維を1〜20重量部及び膨張黒鉛を5〜30重量部配全
部る。この条件を満した時に帯電防止効果(表面抵抗値
103〜108Ω)が優れた導電性樹脂組成物が得られ
る。
The blending amounts are 1 to 20 parts by weight of the conductive fiber and 5 to 30 parts by weight of the expanded graphite to 100 parts by weight of the resin. When this condition is satisfied, a conductive resin composition with excellent antistatic effect (surface resistance value of 10 3 to 10 8 Ω) can be obtained.

膨張黒鉛の使用量は、5重量部より少ないと十分な帯電
防止効果が得られず好ましくない。
If the amount of expanded graphite used is less than 5 parts by weight, a sufficient antistatic effect cannot be obtained, which is not preferable.

又、30重量部をこえた場合には、帯電防止効果が更に
向上せず30重量部以上加える必要はない。
Moreover, if the amount exceeds 30 parts by weight, the antistatic effect will not be further improved, so there is no need to add more than 30 parts by weight.

導電性繊維の使用量は1重量部より少ないと、電磁波遮
蔽効果及び帯電防止効果が著しく低下して好ましくない
、又、20重量部より多い場合には、得られる導電性樹
脂組成物の耐衝撃性、引張強度、成形性等の物性が低下
して好ましくない。
If the amount of conductive fiber used is less than 1 part by weight, the electromagnetic wave shielding effect and antistatic effect will be significantly reduced, which is undesirable. If it is more than 20 parts by weight, the impact resistance of the resulting conductive resin composition will be reduced. Physical properties such as hardness, tensile strength, and moldability deteriorate, which is undesirable.

本発明の組成物は、表面抵抗値が10”〜lO@ Ωの
範囲で安定した値を示し、しかも、淡色であるから任意
の着色剤を添加することで所望の色調に着色可能であり
、カラフルなプラスチックの成形品が製造できる。しか
も、得られる成形品の表面抵抗値は、着色剤を添加せぬ
ものと殆んど変らない。
The composition of the present invention exhibits a stable surface resistance value in the range of 10'' to 1O@Ω, and is light in color, so it can be colored into a desired color by adding any coloring agent. Colorful plastic molded products can be produced.Moreover, the surface resistance of the resulting molded products is almost the same as that without the addition of a colorant.

従って、本発明による帯電防止効果の優れた導電性樹脂
組成物は、tC用マガジン、IC用トレー等の帯電防止
部品、半導体関係の梱包及び収納容器、自動車内部品、
あるいは防塵を必要とする部品等に使用できる。
Therefore, the conductive resin composition with excellent antistatic effect according to the present invention can be used for antistatic parts such as TC magazines, IC trays, semiconductor-related packaging and storage containers, automobile interior parts, etc.
Alternatively, it can be used for parts that require dustproofing.

尚、本発明の組成物を着色する際に使用する染顔料は、
従来より樹脂の着色に使用されているものであればどれ
でも良い、又染顔料の易分散化の目的で脂肪酸、脂肪酸
金属塩、低分子量ポリマー、脂肪酸ワックス等を添加し
てもよい。
In addition, the dyes and pigments used when coloring the composition of the present invention are:
Any of those conventionally used for coloring resins may be used, and fatty acids, fatty acid metal salts, low molecular weight polymers, fatty acid waxes, etc. may be added for the purpose of easily dispersing dyes and pigments.

以下に、実施例及び比較例を述べる。Examples and comparative examples will be described below.

実施例I Ml値8、密度0.9のポリプロピレン樹脂100重量
部に対して、嵩密度0.018g/ccの膨張黒鉛′(
日本黒鉛社製) 13重量部及びポリアクリロニトリル
系炭素繊維(商品名:トレカT−008、東し社製) 
13重量部を配合し、40■−単軸押出機(フルフライ
トL/El−28)で混練して、ペレット化した本願発
明の導電性樹脂組成物(表面抵抗値1.2 XIO’Ω
、ASTMD−257により測定)を得る。
Example I Expanded graphite'(
(manufactured by Nippon Graphite Co., Ltd.) 13 parts by weight and polyacrylonitrile carbon fiber (product name: Torayca T-008, manufactured by Toshisha Co., Ltd.)
13 parts by weight of the conductive resin composition of the present invention (surface resistance value 1.2
, measured according to ASTM D-257).

このペレット125重量部に、酸化チタン6重量部、銅
フタロシアニンブルー0.6重量部及び金属石けん0.
6重量部からなる着色剤(ドライカラー)を混合して、
射出成形機により80X160X3mの試験片を成形し
たところ、色調は淡いブルーであった。
To 125 parts by weight of these pellets, 6 parts by weight of titanium oxide, 0.6 parts by weight of copper phthalocyanine blue, and 0.6 parts by weight of metal soap.
Mixing a coloring agent (dry color) consisting of 6 parts by weight,
When a test piece measuring 80 x 160 x 3 m was molded using an injection molding machine, the color tone was pale blue.

この試験片の(イ)表面抵抗値、(I+)体積固有抵抗
値及び(八)成形性について、測定し、結果を第1表に
しめす。
The test pieces were measured for (a) surface resistance, (I+) volume resistivity, and (viii) formability, and the results are shown in Table 1.

尚、測定法は次の通りである。The measurement method is as follows.

(イ)表面抵抗値 ASTM  D−257に準じて測定する。(a) Surface resistance value Measured according to ASTM D-257.

(0)体積固有抵抗値 日本ゴム境界規格、5RIS−2301に準じて測定す
る。
(0) Volume resistivity value Measured according to Japan Rubber Boundary Standard, 5RIS-2301.

(ハ)半減時間 JIS−L−1094に準じて測定する。(c) Half-life time Measured according to JIS-L-1094.

(=)成形性 射出成形の安定性、成形品の外観及び寸法精度を総合的
に判断する。
(=)Moldability Comprehensively evaluates the stability of injection molding, the appearance and dimensional accuracy of the molded product.

◎・・・・・・非常に良好、○・・・・・・良好×・・
・・・・不良 実施例2 ABS樹脂(商品名: GR−1000、電気化学工業
社製)100重量部に、嵩密度9.020g/ccの膨
張黒鉛(日本黒鉛社製)13重量部及びポリアクリロニ
トリル系炭素繊維(商品名:トレカT−008、東し社
製)13fi量部を配合し、40鰭単軸押出機(フルフ
ライト、L/D−28)で混練してペレット化した本願
発明の導電性樹脂組成物(表面抵抗値1.8 X 10
”Ω)を得る。このペレット125重量部に、酸化チタ
ン5重!1部、キナクリドンレッド(商品名:RT−7
90D。
◎...Very good, ○...Good×...
...Bad Example 2 100 parts by weight of ABS resin (product name: GR-1000, manufactured by Denki Kagaku Kogyo Co., Ltd.), 13 parts by weight of expanded graphite (manufactured by Nippon Graphite Co., Ltd.) with a bulk density of 9.020 g/cc, and polyester were added. The present invention is prepared by blending 13 parts of acrylonitrile carbon fiber (trade name: Torayca T-008, manufactured by Toshisha Co., Ltd.) and kneading it into pellets using a 40-fin single-screw extruder (Full Flight, L/D-28). conductive resin composition (surface resistance value 1.8 x 10
To 125 parts by weight of this pellet, 1 part of titanium oxide 5-fold!, quinacridone red (trade name: RT-7) is obtained.
90D.

デュポン社製)0.6重量部及び金属石けん0.6重量
部からなる着色剤(ドライカラー)を混合し、射出成形
機により80X160X3龍の試験片を成形したところ
、色調は淡い赤色であった。
When a coloring agent (dry color) consisting of 0.6 parts by weight (manufactured by DuPont) and 0.6 parts by weight of metal soap was mixed and an 80 x 160 x 3 dragon test piece was molded using an injection molding machine, the color tone was pale red. .

以後、実施例1と同様なテストを行い結果を第1表に示
す。
Thereafter, tests similar to those in Example 1 were conducted and the results are shown in Table 1.

実施例3 実施例1で使用のポリプロピレン樹脂をME値6.5、
密度0.95の嵩密度ポリエチレンにかえる以外は、実
施例1と配合は全べて同じである。
Example 3 The polypropylene resin used in Example 1 had an ME value of 6.5,
All formulations were the same as in Example 1 except for changing to bulk density polyethylene with a density of 0.95.

尚、本願発明の導電性樹脂組成物の表面抵抗値は1.5
 X 10”Ωである。
The surface resistance value of the conductive resin composition of the present invention is 1.5.
X 10”Ω.

以後、実施例1と同様なテストを行い結果を第1表に示
す。
Thereafter, tests similar to those in Example 1 were conducted and the results are shown in Table 1.

実施例4 ナイロン樹脂(商品名:ウベナイロン66B2020、
宇部興産社製品)100重量部に炭素繊維(商品名:パ
イロフィルX 7006KA三菱レイヨン社製品)10
1i1部、嵩密度0.018g/ccの膨張黒鉛(日本
黒鉛社製)10重量部、銅フタロシアニンブルー1fE
量部及び、ステアリン酸カルシウム1重量部を混合し、
40fiのスクリューベント押出機によりペレットを得
る このペレットを80℃で5時間乾燥後、射出成形機によ
り80X160x3mmの試験片を成形したところ、色
調はブルーであった。
Example 4 Nylon resin (product name: Ube Nylon 66B2020,
100 parts by weight of carbon fiber (product name: Pyrofil X 7006KA Mitsubishi Rayon product)
1i 1 part, expanded graphite with a bulk density of 0.018 g/cc (manufactured by Nippon Graphite Co., Ltd.) 10 parts by weight, copper phthalocyanine blue 1fE
and 1 part by weight of calcium stearate,
Pellets were obtained using a 40fi screw vent extruder. After drying the pellets at 80°C for 5 hours, test pieces of 80 x 160 x 3 mm were molded using an injection molding machine, and the color tone was blue.

以後、実施例1と同様なテストを行い結果を第1表に示
す。
Thereafter, tests similar to those in Example 1 were conducted and the results are shown in Table 1.

比較例1 実施例1での膨張黒鉛の使用量を2重部とする以外、他
の配合については実施例1と同じである。
Comparative Example 1 The other formulations were the same as in Example 1 except that the amount of expanded graphite used in Example 1 was 2 parts.

尚、着色剤を配合する前の組成物の表面抵抗値は1.2
 X 10’ Ωである。以後、実施例1と同様なテス
トを行い結果を第1表に示す。
The surface resistance value of the composition before adding the colorant is 1.2.
X 10'Ω. Thereafter, tests similar to those in Example 1 were conducted and the results are shown in Table 1.

比較例2 実施例1でのポリアクリロニトリル系炭素繊維の使用量
を0.5重量部とする以外は、実施例1の配合と同じで
ある。
Comparative Example 2 The formulation was the same as in Example 1 except that the amount of polyacrylonitrile carbon fiber used in Example 1 was changed to 0.5 parts by weight.

尚、着色剤を配合する前の組成物の表面抵抗値は> 1
0’Ωである。以後、実施例1と同様なテストを行い結
果を第1表に示す。
The surface resistance value of the composition before adding the colorant is > 1
It is 0'Ω. Thereafter, tests similar to those in Example 1 were conducted and the results are shown in Table 1.

比較例3 実施例1でのポリアクリロニトリル系炭素繊維の使用量
を25重量部とする以外は、実施例1の配合と同じであ
る。
Comparative Example 3 The formulation was the same as in Example 1 except that the amount of polyacrylonitrile carbon fiber used in Example 1 was changed to 25 parts by weight.

尚、着色剤を配合する前の組成物の表面抵抗値は9.6
X10−”Ωである。以後、実施例1と同様なテストを
行い結果を第1表に示す。
The surface resistance value of the composition before adding the colorant was 9.6.
X10-''Ω. Thereafter, tests similar to those in Example 1 were conducted and the results are shown in Table 1.

第1表 以上、第1表から理解されるように、本願発明の着色可
能な導電性樹脂組成物は、各種着色剤(ドライカラー、
マスターバッチ等)の添加により希望する色調が得られ
、調色した後でも、半減時間が2〜3秒と帯電防止効果
に優れている。
As can be understood from Table 1 and above, the colorable conductive resin composition of the present invention can be used with various colorants (dry color,
A desired color tone can be obtained by adding a masterbatch, etc.), and even after toning, the half-life time is 2 to 3 seconds, and the antistatic effect is excellent.

Claims (1)

【特許請求の範囲】 熱可塑性樹脂100重量部に対して、導電 性繊維1〜20重量部及び膨張黒鉛5〜30重量部を配
合することを特徴とする着色可能な導電性樹脂組成物。
[Scope of Claims] A colorable conductive resin composition, characterized in that 1 to 20 parts by weight of conductive fibers and 5 to 30 parts by weight of expanded graphite are blended with 100 parts by weight of a thermoplastic resin.
JP15511186A 1986-07-03 1986-07-03 Colorable electrically conductive resin composition Pending JPS6312663A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP15511186A JPS6312663A (en) 1986-07-03 1986-07-03 Colorable electrically conductive resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP15511186A JPS6312663A (en) 1986-07-03 1986-07-03 Colorable electrically conductive resin composition

Publications (1)

Publication Number Publication Date
JPS6312663A true JPS6312663A (en) 1988-01-20

Family

ID=15598833

Family Applications (1)

Application Number Title Priority Date Filing Date
JP15511186A Pending JPS6312663A (en) 1986-07-03 1986-07-03 Colorable electrically conductive resin composition

Country Status (1)

Country Link
JP (1) JPS6312663A (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01319549A (en) * 1988-06-22 1989-12-25 Showa Denko Kk Resin composition
JPH048767A (en) * 1990-04-27 1992-01-13 Dainippon Ink & Chem Inc Thermoplastic resin composition
WO1999020563A1 (en) * 1997-10-16 1999-04-29 Universiteit Utrecht Graphitic material loaded with alkali metal
US6794078B1 (en) * 1999-12-06 2004-09-21 Hitachi Chemical Company, Ltd. Fuel cell, fuel cell separator, and method of manufacture thereof
KR101088528B1 (en) * 2002-07-23 2011-12-05 사빅 이노베이티브 플라스틱스 아이피 비.브이. Conductive Thermoplastic Composite and Method for Manufacturing the Same
JP2012036247A (en) * 2010-08-04 2012-02-23 Toray Ind Inc Resin composition
EP3714003A4 (en) * 2017-11-20 2021-08-04 Ticona LLC Fiber-reinforced polymer composition for use in an electronic module
US11129312B2 (en) 2017-11-20 2021-09-21 Ticona Llc Electronic module for use in an automotive vehicle

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01319549A (en) * 1988-06-22 1989-12-25 Showa Denko Kk Resin composition
JPH048767A (en) * 1990-04-27 1992-01-13 Dainippon Ink & Chem Inc Thermoplastic resin composition
WO1999020563A1 (en) * 1997-10-16 1999-04-29 Universiteit Utrecht Graphitic material loaded with alkali metal
US6794078B1 (en) * 1999-12-06 2004-09-21 Hitachi Chemical Company, Ltd. Fuel cell, fuel cell separator, and method of manufacture thereof
KR101088528B1 (en) * 2002-07-23 2011-12-05 사빅 이노베이티브 플라스틱스 아이피 비.브이. Conductive Thermoplastic Composite and Method for Manufacturing the Same
JP2012036247A (en) * 2010-08-04 2012-02-23 Toray Ind Inc Resin composition
EP3714003A4 (en) * 2017-11-20 2021-08-04 Ticona LLC Fiber-reinforced polymer composition for use in an electronic module
US11129312B2 (en) 2017-11-20 2021-09-21 Ticona Llc Electronic module for use in an automotive vehicle
US11466130B2 (en) 2017-11-20 2022-10-11 Ticona Llc Fiber-reinforced polymer composition for use in an electronic module

Similar Documents

Publication Publication Date Title
US4569786A (en) Electrically conductive thermoplastic resin composition containing metal and carbon fibers
US20030055154A1 (en) Conductive resin composition and process for producing the same
EP1842879A1 (en) Polyamide resin composition and conductive shaft-shaped molded article
JPS6312663A (en) Colorable electrically conductive resin composition
JP3960096B2 (en) Conductive resin composition and method for producing the same
JP4948722B2 (en) Resin composition having metallic luster
JPS60144367A (en) Electrically conductive resin composition
JP3487034B2 (en) PBT resin molding material
JP2003012945A (en) Conductive resin composition and method for producing the same
JPH069819A (en) Resin composition for electromagnetic wave shielding
JPS6220540A (en) Conductive resin composition
JPS5889645A (en) Thermoplastic polyester composition
JP3406816B2 (en) Thermoplastic resin composition
JPH0379665A (en) Polyamide resin composition
JPS6127411B2 (en)
JPH0570685A (en) Polyamide resin composition
JP2000281896A (en) Flame-retardant conductive resin composition and molded product using the same
EP0279985A2 (en) Electrically conductive thermoplastic resin composition
JPH0873655A (en) Electrically conductive resin composition and its production
JPH02178336A (en) Antistatic molding material
CN104419143A (en) High-tenacity antistatic flame retardant PET/ABS composite material
CN113637305B (en) Low-gloss non-coated thermoplastic resin composition, method for producing molded article using the same, and molded article produced by the method
JPH0684465B2 (en) Method for producing improved colored polybutylene terephthalate resin composition
JPS5811546A (en) Coloring composition for synthetic resin
JPH0160505B2 (en)