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JPS59223735A - Conductive resin composition - Google Patents

Conductive resin composition

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Publication number
JPS59223735A
JPS59223735A JP58096894A JP9689483A JPS59223735A JP S59223735 A JPS59223735 A JP S59223735A JP 58096894 A JP58096894 A JP 58096894A JP 9689483 A JP9689483 A JP 9689483A JP S59223735 A JPS59223735 A JP S59223735A
Authority
JP
Japan
Prior art keywords
coupling agent
silane coupling
metal
resin composition
weight
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
JP58096894A
Other languages
Japanese (ja)
Inventor
Satoshi Matsuura
松浦 智
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.)
Mitsui Petrochemical Industries Ltd
Original Assignee
Mitsui Petrochemical Industries 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 Mitsui Petrochemical Industries Ltd filed Critical Mitsui Petrochemical Industries Ltd
Priority to JP58096894A priority Critical patent/JPS59223735A/en
Publication of JPS59223735A publication Critical patent/JPS59223735A/en
Pending legal-status Critical Current

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  • Compositions Of Macromolecular Compounds (AREA)
  • Conductive Materials (AREA)

Abstract

PURPOSE:An electroconductive resin composition excellent in mechanical strength, rigidity and electric conductivity, and suitable for use as a conductive material of high-voltage cables, obtained by mixing a thermoplastic resin with a metal and a silane coupling agent at a specified weight ratio. CONSTITUTION:The purpose electroconductive resin composition is prepared by mixing 5-95wt% (A) thermoplastic resin such as polyethylene or polypropylene with 95-5wt% (B) metal, e.g., aluminum or copper, in the form of powder, fiber, flake, or the like, and 0.05-5pts.wt., per 100pts.wt. total of components A and B, silane coupling agent, e.g., vinyltrimethoxysilane or gamma-aminopropyltriethoxysilane. A more marked effect can be obtained with a smaller amount of the silane coupling agent by pretreating the metal with the silane coupling agent and adding the treated metal to the thermoplastic resin.

Description

【発明の詳細な説明】 本発明は導電性樹脂組成物に関する。更に詳しくは、シ
ラン系カップリング剤で処理した金属を含んでなる剛性
が改良された導電性樹脂組成物に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a conductive resin composition. More specifically, the present invention relates to a conductive resin composition with improved rigidity that includes a metal treated with a silane coupling agent.

熱可FJ 性m 脂にアルミニウムフレーク等の金属を
配合して導電性を付与することは良く知られている。そ
して導電性樹脂は高圧ケーブルの導電性材料、XC−+
電子レンジ15通信機器等の電磁波遮蔽材、ビデオディ
スク用導電性材料等として広く使用されている。
It is well known that metals such as aluminum flakes are added to thermoplastic FJ resins to impart electrical conductivity. The conductive resin is the conductive material for high voltage cables, XC-+
It is widely used as an electromagnetic wave shielding material for microwave ovens 15 communication equipment, a conductive material for video discs, etc.

しかしながら熱可塑性樹脂は、ポリエチレン、ポリプロ
ピレン等のポリオレフィンを初めポリアミド、ポリエス
テル等の汎用樹脂の殆どは本来絶縁性に優れた材料であ
り、それに導電性を付与するには、多量の金属を配合す
る必要があり、その結果、樹脂本来の特徴である剛性等
の機械的特性の低下を来たす虞れがあった。
However, thermoplastic resins, such as polyolefins such as polyethylene and polypropylene, as well as general-purpose resins such as polyamides and polyesters, are originally materials with excellent insulation properties, and in order to impart conductivity to them, it is necessary to blend a large amount of metal. As a result, there is a risk that the mechanical properties such as rigidity, which are the original characteristics of the resin, may deteriorate.

かかる状況から、本発明者は従来の欠点を有さす、且つ
導電性に優れた樹脂組成物を得るべく種々検討した結果
、熱可塑性樹脂にシラン系カップリング剤で処理した金
属あるいはシラン系カップリング剤と金属とを添加する
ことにより、剛性に優れた導電性樹脂組成物が得られる
ことが分かり本発明に到達した。
Under such circumstances, the present inventor conducted various studies in order to obtain a resin composition with excellent conductivity, which has the disadvantages of the conventional ones.As a result, the present inventor developed a metal or silane-based coupling in which a thermoplastic resin is treated with a silane-based coupling agent. The present invention was achieved based on the discovery that a conductive resin composition with excellent rigidity can be obtained by adding an agent and a metal.

すなわち本発明は、熱可塑性樹脂(〜:5ないし95重
量%−金属(d:+;+5ないし5重量%及び(〜十(
1=100重量部に対してシラン系カップリング剤(C
):0.05ないし5重量部とからなることを特徴とす
る機械的強度及び剛性に優れた導電性樹脂組成物を提供
するものである。
That is, the present invention provides thermoplastic resin (~: 5 to 95% by weight - metal (d: +; +5 to 5% by weight) and (~10 (
1 = 100 parts by weight of silane coupling agent (C
): 0.05 to 5 parts by weight to provide a conductive resin composition having excellent mechanical strength and rigidity.

本発明に用いる熱可塑性樹脂(〜は、佑可塑性を示す樹
脂であれば結晶性、非品性を問わず、低密度ポリエチレ
ン、高密度ポリエチレン、ポリプロピレン、ポリ1−ブ
テン、ポリ4−メチル−1−ペンテンアルいはエチレン
、プロピレン、1−ブテン、4−メチル−1−ペンテン
等のα−オレフィン同志のランダムあるいはブロック共
重合体等のポリオレフィン、エチレン・アクリル酸共重
合体、エチレン・酢酸ビニル共重合体、エチレン・ビニ
ルアルコール共重合体、エチレン・塩化ビニル共重合体
等のエチレン・ビニル化合物共重合体、ポリスチレン、
アクリロニトリル°スチレン共重合体、A B S %
メタクリル酸メチル・スチレン共重合体、α−メチルス
チレン・スチレン共重合体等のスチレン系樹脂、ポリ塩
化ビニル、ポ1)塩化ビニリデン、塩化ビニル・塩化ビ
ニリデン共重合体、ポリアクリル酸メチル、ポリメタク
リル酸メチル等のポリビニル化合物、ナイロン6、ナイ
ロン6−6、ナイロン6−10.ナイロン11、ナイロ
ン12等のポリアミド、ボリエヂレンテしフタレート、
ポリブチレンテレフタレート等の熱可塑性ポリエステル
、ポリカーボネート、ポリフェニレンオキサイド等のい
ずれの樹脂でもよい。
Thermoplastic resins used in the present invention (~ are resins that exhibit plasticity, regardless of whether they are crystalline or non-crystalline); low-density polyethylene, high-density polyethylene, polypropylene, poly-1-butene, poly-4-methyl-1 - Polyolefins such as random or block copolymers of α-olefins such as pentenal or ethylene, propylene, 1-butene, 4-methyl-1-pentene, ethylene/acrylic acid copolymers, ethylene/vinyl acetate copolymers ethylene/vinyl compound copolymers such as ethylene/vinyl alcohol copolymers, ethylene/vinyl chloride copolymers, polystyrene,
Acrylonitrile ° styrene copolymer, AB S %
Styrenic resins such as methyl methacrylate/styrene copolymer, α-methylstyrene/styrene copolymer, polyvinyl chloride, polyvinylidene chloride, vinyl chloride/vinylidene chloride copolymer, polymethyl acrylate, polymethacrylate Polyvinyl compounds such as methyl acid, nylon 6, nylon 6-6, nylon 6-10. Polyamides such as nylon 11 and nylon 12, polyamide phthalate,
Any resin such as thermoplastic polyester such as polybutylene terephthalate, polycarbonate, polyphenylene oxide, etc. may be used.

本発明に用いるシラン系カップリング剤(C)は、オレ
フィン性不飽和結合、アミノ基、水酸基、ヒドロキシア
ルキル する基を持つ有機シラン化合物であり、具体的には、ビ
ニルトリメトキシシラン、ビニルトリエトキシシラン、
ビニルトリス(メトキシエトキシ)シラン、ビニルメチ
ルジェトキシシランェニルジメトキシシラン プロピルトリメトキシシラン、β−アミノフェノキシジ
メチルビニルシラン、r−アミノプロピルトリエトキシ
シラン、r−アミノプロビルジメチフレエトキシシラン
、トリエチルシラノール、ジメチルエトキシシラン、r
−グリシドキシプロビルトリメチルシラン等を例示する
ことができる。中でもビニルトリス(メトキシエトキシ
)シラン、r−メタクリロキシプロピルトリメトキシシ
ラン、γーアミノプロピルトリエトキシシラン、γーグ
リシドキシプロピルトリメトキシシラン等の沸点が20
0°C以上の有機シラン化合物が機械的強度及び剛性等
の改良効果に優れるので好ましい。
The silane coupling agent (C) used in the present invention is an organic silane compound having an olefinic unsaturated bond, an amino group, a hydroxyl group, or a hydroxyalkyl group, and specifically, vinyltrimethoxysilane, vinyltriethoxysilane, etc. silane,
Vinyltris(methoxyethoxy)silane, vinylmethyljethoxysilane phenyldimethoxysilane propyltrimethoxysilane, β-aminophenoxydimethylvinylsilane, r-aminopropyltriethoxysilane, r-aminopropyldimethyfurethoxysilane, triethylsilanol, dimethylethoxy silane, r
-Glycidoxyprobyltrimethylsilane and the like can be exemplified. Among them, vinyltris(methoxyethoxy)silane, r-methacryloxypropyltrimethoxysilane, γ-aminopropyltriethoxysilane, γ-glycidoxypropyltrimethoxysilane, etc. have a boiling point of 20
An organic silane compound having a temperature of 0°C or higher is preferable because it has an excellent effect of improving mechanical strength and rigidity.

本発明に用いる金属CB)は、アルミニウム、鉄、銅、
ニッケル、あるいはそれらの合金であるステンレス、黄
銅、青銅等の粉末状、繊維状、あるいはフレーク状から
なる通常樹脂等の充填剤として混入できる形態を有する
ものである。粉末状物としては通常20ないし250メ
ツシユの範囲、繊維状物としては通常直径が0.001
ないしQ.2mmの範囲で長さが10mm以下のもの、
フレーク状物としては通常断面積が0.IXOlmmな
いし5X5mmの範囲の円形、正方形、長方形、六角形
などの任意の形状のもので、厚さが3.1rom以下の
ものが好適に使用できる。
Metals CB) used in the present invention include aluminum, iron, copper,
Nickel or alloys thereof such as stainless steel, brass, bronze, etc., are usually in the form of powders, fibers, or flakes, and have a form that can be mixed as a filler in resins and the like. Powder-like materials usually range from 20 to 250 meshes, and fibrous materials usually have a diameter of 0.001 mm.
Or Q. Items with a length of 10 mm or less within a range of 2 mm,
The cross-sectional area of flakes is usually 0. Any shape such as circular, square, rectangular, hexagonal, etc. in the range of IXOlmm to 5X5mm and a thickness of 3.1 ROM or less can be suitably used.

本発明の導電性樹脂組成物は、前記熱可塑性樹脂(A)
:5ないし95重量%、好ましくは5Gないし75重量
%、金属(B):95ないし5重量%、好ましくは50
ないし25重量%及び(Al + (B) = + O
 0重量部に対してシラン系カップリング剤0.05な
いし5重量部、好ましくは0.5 ?いし2重量部とか
ら構成される。
The conductive resin composition of the present invention comprises the thermoplastic resin (A)
: 5 to 95% by weight, preferably 5G to 75% by weight, Metal (B): 95 to 5% by weight, preferably 50
to 25% by weight and (Al + (B) = + O
0.05 to 5 parts by weight, preferably 0.5 parts by weight of the silane coupling agent. 2 parts by weight.

金属(B)の量が5重量%未満では導電性の改良効2り 果がなく、輔重量%を越えると、溶融時の流動性が悪く
成形性に劣り、且つ成形品の機械的強度が低下する。
If the amount of metal (B) is less than 5% by weight, there will be no effect of improving conductivity, and if it exceeds 5% by weight, the fluidity during melting will be poor, the moldability will be poor, and the mechanical strength of the molded product will decrease. descend.

シラン系カップリング剤(C)の量が0−05ffif
fi部未満では組成物の機械的強度、剛性が改良されず
、5重量部を越えると効果が飽和してしまう。
The amount of silane coupling agent (C) is 0-05ffif
If it is less than fi part, the mechanical strength and rigidity of the composition will not be improved, and if it exceeds 5 parts by weight, the effect will be saturated.

本発明の導電性樹脂組成物には、前記構成成分の他に、
耐熱安定剤、耐候安定剤、核剤、可塑剤、’III 燃
剤、タルク、炭酸カルシウム、マイカ、微粉末シリカ、
硫酸バリウム、ウオラストナイト、クレー、カオリン、
黒鉛、チタン酸カリウムウィスカー等の無機充填剤、顔
料、染料等通常熱可塑性樹脂に添加して使用される配合
剤を本発明の目的を損わない範囲で配合しておいてもよ
い。
In addition to the above-mentioned components, the conductive resin composition of the present invention includes:
Heat stabilizer, weather stabilizer, nucleating agent, plasticizer, 'III retardant, talc, calcium carbonate, mica, finely powdered silica,
barium sulfate, wollastonite, clay, kaolin,
Inorganic fillers such as graphite and potassium titanate whiskers, pigments, dyes, and other compounding agents that are normally added to thermoplastic resins may be included within the range that does not impair the purpose of the present invention.

本発明の導電性樹脂組成物を製造するには、予め金属(
旬をシラン系カップリング剤(C)で処理してから熱可
塑性樹脂(→に配合する方法、あるいは熱可塑性樹脂(
A)と金属(B)及びシラン系カップリング剤(C)と
を同時に混合する方法が採り得るが、シラン系カップリ
ング剤(C)の添加量を少なくして効果を上げられる点
では前者の方法が好ましい。
To produce the conductive resin composition of the present invention, metal (
A method of treating shun with a silane coupling agent (C) and then adding it to a thermoplastic resin (→), or a method of adding a thermoplastic resin (
Although it is possible to simultaneously mix A) with the metal (B) and the silane coupling agent (C), the former method is preferable in that it can increase the effect by reducing the amount of the silane coupling agent (C) added. The method is preferred.

前者の方法としては、例えばヘンシェルミキサーで金属
(橡を攪拌しなからシラン系カップリング剤(C)、あ
るいは溶剤に溶解したシラン系カップリング剤(C)を
添加し、もしくは金属((2)とシラン系カップリング
剤(C)とを同時に混合攪拌して、金属表面にシラン系
カップリング剤を付着させた後、必要に応じて乾燥させ
、次いで熱可塑性樹脂(〜と再度ヘンシェルミキサー、
■−ブレンダー、タンブラーブレンダー、リボンプレン
ダー等で混合後、バンバリーミキサ−、ニーグー、ロー
IV、単tdJn出機、多軸押出機等で混練後、粉砕あ
るいは造粒する方法が例示できる。
The former method involves, for example, adding a silane coupling agent (C) or a silane coupling agent (C) dissolved in a solvent to the metal (2) without stirring the metal (2) using a Henschel mixer. and the silane coupling agent (C) are simultaneously mixed and stirred to adhere the silane coupling agent to the metal surface, dried if necessary, and then mixed with the thermoplastic resin (~ and the Henschel mixer again,
(2) - Mixing with a blender, tumbler blender, ribbon blender, etc., followed by kneading with a Banbury mixer, Nigoo, Rho IV, single tdJn extruder, multi-screw extruder, etc., followed by pulverization or granulation can be exemplified.

また後者の方法としては、熱可塑性樹脂(A)、金属(
旬及びシラン系カップリング剤(C)とをヘンシェルミ
キサー、■−プレンダー、タンブラーブレンダー、リボ
ンプレンダー等で混合後、前記と同様に混練後、粉砕あ
るいは造粒する方法が例示できる。
In the latter method, thermoplastic resin (A), metal (
An example of a method is to mix the mixture with the silane coupling agent (C) using a Henschel mixer, a -blender, a tumbler blender, a ribbon blender, etc., knead in the same manner as described above, and then pulverize or granulate.

本発明の導電性樹脂組成物は導電性を有し、機械的強度
及び剛性に優れ且つ成形性も良好であるので、射出成形
、押出成形、圧縮成形、熱成形等により成形後、建築物
の外壁、内装材、テレビ、ヒテオ、電子計算機、ワード
プロセッサーなどのハウジング材、自動車電子装置、機
器等の電磁遮蔽性が必要な用途に好適に使用することが
できる。
The conductive resin composition of the present invention has conductivity, excellent mechanical strength and rigidity, and good moldability. It can be suitably used for applications that require electromagnetic shielding properties, such as exterior walls, interior materials, housing materials for televisions, HDTVs, electronic computers, word processors, etc., automobile electronic devices, and equipment.

次に実施例によって本発明を更に具体的に説明する。Next, the present invention will be explained in more detail with reference to Examples.

実施例1 ポリプロピレン(商品名 三井石油化学ポリプロ■SJ
a+oD  >aFa:15g/10m1n三井石油化
学工業(株)製)のパウダーエフ0重量%と、ビ1; ニルトリエトキシシラン(沸点161°C): 0.3
重量部で処理したアルミニウムフレーク(トランスメッ
ト社製〕:60重量%とをヘンシェルミキサーで混合後
40mmφ押出機(樹脂温度250°C〕で溶融混練造
粒して組成物−■を得た。次いで組成物−■を用いて、
射出成形機(Is−50東芝機械(株)製:成形温度2
60°C)で射出成形して試験片を得た。
Example 1 Polypropylene (trade name Mitsui Petrochemical Polypro SJ
a+oD>aFa: 15g/10ml 0% by weight of Powder F (manufactured by Mitsui Petrochemical Industries, Ltd.) and Bi1; Nyltriethoxysilane (boiling point 161°C): 0.3
Aluminum flakes treated in parts by weight (manufactured by Transmet): 60% by weight were mixed in a Henschel mixer and then melt-kneaded and granulated in a 40 mmφ extruder (resin temperature 250°C) to obtain composition -1. Using composition-■,
Injection molding machine (Is-50 manufactured by Toshiba Machine Co., Ltd.: Molding temperature 2
A test piece was obtained by injection molding at 60°C.

以下試験片の評価を次の方法で行った。The test pieces were evaluated in the following manner.

引張試験: ASTM D638 曲げ試験: ASTM D790 アイゾツト街撃試験: ASTM D256、ノツチ付
き 体積固有抵抗試験:抵抗計(タケダ理研社製 。
Tensile test: ASTM D638 Bending test: ASTM D790 Izod impact test: ASTM D256, notched volume resistivity test: Resistance meter (manufactured by Takeda Riken Co., Ltd.).

TR−6856)を用い、温度25°C1湿度60%の
雰囲気下で厚さが2mmのシートの抵抗を測定し、下式
に従って算出した。
TR-6856), the resistance of a sheet with a thickness of 2 mm was measured in an atmosphere of 25° C. and 60% humidity, and calculated according to the formula below.

XR 体積固有抵抗(Ω・CTn)−− ここで、S:固有抵抗率測定電極の電極面積(on勺 R:シートの抵抗値(Ω) t:シートの厚さくcln) を表わす。XR Volume resistivity (Ω・CTn) -- Here, S: electrode area of specific resistivity measuring electrode R: Sheet resistance value (Ω) t: sheet thickness cln) represents.

結果を第1表に示す。The results are shown in Table 1.

実施例2 実施例1で用いたビニルトリエトキシシランの代わりに
ビニルトリス(メトキシエトキシ)シラン(沸点285
°C)を用いる以外は実施例1と同様に行った。結果を
第1表に示す。
Example 2 Vinyltris(methoxyethoxy)silane (boiling point 285
The same procedure as in Example 1 was carried out except that the temperature (°C) was used. The results are shown in Table 1.

実施例3 実施例1で用いたビニルトリエトキシシランの代わりに
γ−メタクリロキシプロピルトリメトキシシラン(沸点
255”C)を用いる以外は実施例1と同様に行った。
Example 3 The same procedure as in Example 1 was carried out except that γ-methacryloxypropyltrimethoxysilane (boiling point 255"C) was used instead of the vinyltriethoxysilane used in Example 1.

結果を第1表に示す。The results are shown in Table 1.

実施例4 実m例1で用いたビニルトリエトキシシランの代わりに
r−アミノプロピルトリエトキシシラン(沸点217°
C)を用いる以外は実施例1と同様に行った。結果を第
1表に示す。
Example 4 In place of the vinyltriethoxysilane used in Example 1, r-aminopropyltriethoxysilane (boiling point 217°
The same procedure as in Example 1 was carried out except that C) was used. The results are shown in Table 1.

比較例1 実施例1で用いたビニルトリエトキシシランで処理した
アルミニウムフレークの代わりに、無処理のアルミニウ
ムフレークを用いる以外は実施例1と同様に行った。結
果を第1表に示す。
Comparative Example 1 The same procedure as in Example 1 was conducted except that untreated aluminum flakes were used instead of the aluminum flakes treated with vinyltriethoxysilane used in Example 1. The results are shown in Table 1.

比較例2 実施例1で用いたビニルトリエトキシシランの代わりに
イソプロピルトリデシルベンゼンスルホニルチタネ−ト
Comparative Example 2 Isopropyltridecylbenzenesulfonyl titanate was used instead of vinyltriethoxysilane used in Example 1.

Claims (1)

【特許請求の範囲】[Claims] (1)熱可塑性樹脂(〜:5ないし95重量%、金属C
B):95ないし5重量%及び(A)+(B)=100
重量部に対してシラン系カップリング剤(C)=0.0
5ないし5重量部とからなることを特徴とする導電性樹
脂組成物。
(1) Thermoplastic resin (~: 5 to 95% by weight, metal C
B): 95 to 5% by weight and (A)+(B)=100
Silane coupling agent (C) = 0.0 based on weight part
5 to 5 parts by weight of a conductive resin composition.
JP58096894A 1983-06-02 1983-06-02 Conductive resin composition Pending JPS59223735A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58096894A JPS59223735A (en) 1983-06-02 1983-06-02 Conductive resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58096894A JPS59223735A (en) 1983-06-02 1983-06-02 Conductive resin composition

Publications (1)

Publication Number Publication Date
JPS59223735A true JPS59223735A (en) 1984-12-15

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JP58096894A Pending JPS59223735A (en) 1983-06-02 1983-06-02 Conductive resin composition

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JP (1) JPS59223735A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62104870A (en) * 1985-10-31 1987-05-15 Fujikura Ltd Electrically conductive resin composition
JPH03122162A (en) * 1989-10-06 1991-05-24 Nichiban Kenkyusho:Kk Antibacterial electroconductive composition and antibacterial electroconductive resin
EP0735163A1 (en) * 1995-03-29 1996-10-02 Teijin Limited Electroconductive conjugate fiber
US5654096A (en) * 1995-03-30 1997-08-05 Teijin Limited Electroconductive conjugate fiber
JPWO2021075551A1 (en) * 2019-10-18 2021-04-22

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5248143A (en) * 1975-10-13 1977-04-16 Thermo Electron Corp Water heater
JPS5562938A (en) * 1978-11-02 1980-05-12 Matsushita Electric Ind Co Ltd Electrically conductive resin

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5248143A (en) * 1975-10-13 1977-04-16 Thermo Electron Corp Water heater
JPS5562938A (en) * 1978-11-02 1980-05-12 Matsushita Electric Ind Co Ltd Electrically conductive resin

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62104870A (en) * 1985-10-31 1987-05-15 Fujikura Ltd Electrically conductive resin composition
JPH03122162A (en) * 1989-10-06 1991-05-24 Nichiban Kenkyusho:Kk Antibacterial electroconductive composition and antibacterial electroconductive resin
EP0735163A1 (en) * 1995-03-29 1996-10-02 Teijin Limited Electroconductive conjugate fiber
US5654096A (en) * 1995-03-30 1997-08-05 Teijin Limited Electroconductive conjugate fiber
JPWO2021075551A1 (en) * 2019-10-18 2021-04-22
CN114514284A (en) * 2019-10-18 2022-05-17 本田技研工业株式会社 Resin composition, resin molded article comprising same, and method for producing resin molded article
CN114514284B (en) * 2019-10-18 2024-09-24 本田技研工业株式会社 Resin composition, resin molded body comprising same, and method for producing resin molded body

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