JPH08198999A - Electroconductive resin composition - Google Patents

Electroconductive resin composition

Info

Publication number
JPH08198999A
JPH08198999A JP1068695A JP1068695A JPH08198999A JP H08198999 A JPH08198999 A JP H08198999A JP 1068695 A JP1068695 A JP 1068695A JP 1068695 A JP1068695 A JP 1068695A JP H08198999 A JPH08198999 A JP H08198999A
Authority
JP
Japan
Prior art keywords
resin
carbon black
resin composition
weight
packaging
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
JP1068695A
Other languages
Japanese (ja)
Other versions
JP3308748B2 (en
Inventor
Kenji Miyagawa
健志 宮川
Mikio Shimizu
美基雄 清水
Kenji Nabeta
健司 鍋田
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.)
Denka Co Ltd
Original Assignee
Denki Kagaku Kogyo KK
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
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Application filed by Denki Kagaku Kogyo KK filed Critical Denki Kagaku Kogyo KK
Priority to JP01068695A priority Critical patent/JP3308748B2/en
Publication of JPH08198999A publication Critical patent/JPH08198999A/en
Priority to US08/834,297 priority patent/US5707699A/en
Priority to US08/917,606 priority patent/US5876632A/en
Priority to US09/199,489 priority patent/US5955164A/en
Application granted granted Critical
Publication of JP3308748B2 publication Critical patent/JP3308748B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Compositions Of Macromolecular Compounds (AREA)
  • Structures Or Materials For Encapsulating Or Coating Semiconductor Devices Or Solid State Devices (AREA)
  • Conductive Materials (AREA)

Abstract

PURPOSE: To provide an electroconductive resin composition which comprises a polyphenylene ether resin and the like, carbon black and an ethylene-α-olefin copolymer resin, thus is useful for packaging IC because it is improved in staining of IC or the like with carbon black migrating from the resin by abrasion. CONSTITUTION: (A) 100 pts.wt. of at least one of thermoplastic resin selected from among poly(phenylene ether), polystyrene resin and ABS resin are combined with (B) 5 50 pts.wt. of carbon black, further, 100 pts.wt. of the composition are mixed with (C) 1-30 pts.wt. of an ethylene-α-olefin copolymer resin of less than 90 surface hardness measured with the durometer type A according to JIS K-7215 to give this electroconductive resin composition which is suitable for packaging.IC because it has a surface resistivity of 10<2> -10<10> ohms and markedly reduces the staining of IC or the like with carbon black migrating from the resin by abrasion on the contact with IC or the like.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、ポリフェニレンエーテ
ル系樹脂、ポリスチレン系樹脂又はABS系樹脂の少な
くとも1種類から選ばれた熱可塑性樹脂及びカーボンブ
ラックからなるIC包装用導電性樹脂組成物において、
この導電性樹脂組成物にエチレン−α−オレフィン共重
合体樹脂を含有させることにより、IC等との接触時の
摩耗によるカーボンブラック等の脱離が原因となるIC
等の汚染を著しく減少させたIC包装用導電性樹脂組成
物に関する。
FIELD OF THE INVENTION The present invention relates to a conductive resin composition for IC packaging which comprises a thermoplastic resin selected from at least one kind of polyphenylene ether resin, polystyrene resin or ABS resin and carbon black.
By incorporating an ethylene-α-olefin copolymer resin in this conductive resin composition, IC causing desorption of carbon black or the like due to abrasion at the time of contact with the IC or the like
The present invention relates to a conductive resin composition for IC packaging, in which contamination such as the like is remarkably reduced.

【0002】[0002]

【従来の技術】従来からICやICを用いた電子部品の
包装形態としてインジェクショントレー、真空成形トレ
ー、マガジン、エンボスキャリアテープなどが使用され
ており、これらの包装容器には静電気によるIC等の破
壊を防止するために(1)包装容器の表面に帯電防止剤
を塗布する方法、(2)導電性塗料を塗布する方法、
(3)帯電防止剤若しくは導電性フィラーを分散させる
方法等が実施されている。
2. Description of the Related Art Conventionally, injection trays, vacuum forming trays, magazines, embossed carrier tapes, etc. have been used as packaging forms for ICs and electronic parts using ICs, and these packaging containers are damaged by static electricity. (1) a method of applying an antistatic agent on the surface of the packaging container, and (2) a method of applying a conductive paint,
(3) A method of dispersing an antistatic agent or a conductive filler is implemented.

【0003】しかしながら、(1)の方法は、塗布直後
は十分な帯電防止効果を示すが、長時間の使用により、
水分による流出、摩耗による帯電防止剤の脱離が生じ易
く安定した性能が得られない。また表面固有抵抗値も1
9〜1012Ω程度であり厳しい帯電防止効果を要求さ
れるICの包装には不適当である。 (2)の方法は、製造において塗布が不均一となり易く
また摩耗による剥がれ落ちのため帯電防止効果を失いI
Cを破壊すると共にICのリード部を汚染するという欠
点がある。 (3)の方法においては帯電防止剤では、添加量が多量
に必要のため樹脂の物性を低下させ、また表面固有抵抗
値が湿度により大きく影響され安定した性能が得られな
い。
However, the method (1) has a sufficient antistatic effect immediately after coating, but after a long time of use,
Stable performance cannot be obtained because the antistatic agent is liable to be released due to water outflow and abrasion. The surface resistivity is also 1
It is about 0 9 to 10 12 Ω, which is unsuitable for IC packaging that requires a strict antistatic effect. In the method (2), the coating tends to be non-uniform in the manufacturing process, and the antistatic effect is lost due to peeling off due to abrasion.
It has the drawback of destroying C and contaminating the leads of the IC. In the method (3), the antistatic agent requires a large amount to be added, so that the physical properties of the resin are deteriorated, and the surface resistivity is greatly affected by humidity, so that stable performance cannot be obtained.

【0004】又、導電性フィラーとしては金属微粉末、
カーボンファイバー、カーボンブラックなどが挙げられ
る。この内金属微粉末及びカーボンファイバーは、少量
の添加で十分な導電性が得られるが成形性が著しく低下
し、また均一に分散させることが難しく、かつ成形品の
表面に樹脂成分のみのスキン層が出来易く安定した表面
固有抵抗値が得られにくい。これらに対しカーボンブラ
ックは混練条件等の検討により均一に分散させることが
可能であり、安定した表面固有抵抗値が得られ易いこと
から一般的に使用されていが、カーボンブラックを多量
に添加する必要が有るため流動性や成形性が低下する現
象がある。
As the conductive filler, fine metal powder,
Examples thereof include carbon fiber and carbon black. The metal fine powder and the carbon fiber have sufficient conductivity even if added in a small amount, but the moldability remarkably deteriorates, and it is difficult to disperse them uniformly, and a skin layer containing only a resin component on the surface of the molded product. It is difficult to obtain a stable surface resistivity value. On the other hand, carbon black is generally used because it is possible to disperse it uniformly by studying the kneading conditions, etc. and it is easy to obtain a stable surface resistivity value, but it is necessary to add a large amount of carbon black. There is a phenomenon that fluidity and moldability are deteriorated due to the presence of

【0005】従来、カーボンブラックを分散させる樹脂
としては、一般用としてポリ塩化ビニル系樹脂、ポリプ
ロピレン系樹脂、ポリエチレンテレフタレート系樹脂、
ポリスチレン系樹脂及びABS系樹脂が、また100℃
以上での耐熱用としてポリフェニレンエーテル系樹脂、
ポリカーボネート樹脂などが用いられている。これらの
樹脂のなかで、耐熱用としてはポリフェニレンエーテル
系樹脂が、一般用としてはポリスチレン系樹脂及びAB
S系樹脂が、カーボンブラックを多量に添加しても流動
性や成形性の著しい低下がなく、さらにコストの面でも
優れている。しかしながら、カーボンブラックを多量に
添加した組成物の成形品は、摩耗により成形品の表面か
ら、カーボンブラックが脱離し易いという欠点があっ
た。
Conventionally, as a resin for dispersing carbon black, polyvinyl chloride resin, polypropylene resin, polyethylene terephthalate resin,
Polystyrene resin and ABS resin are 100 ℃
Polyphenylene ether resin for heat resistance above,
Polycarbonate resin or the like is used. Among these resins, polyphenylene ether resins are used for heat resistance, and polystyrene resins and AB for general use.
The S-based resin is excellent in terms of cost without significant deterioration in fluidity and moldability even when a large amount of carbon black is added. However, the molded product of the composition to which a large amount of carbon black is added has a drawback that carbon black is easily detached from the surface of the molded product due to abrasion.

【0006】[0006]

【発明が解決しようとする課題】本発明は、かかる欠点
を解決するものであり、ポリフェニレンエーテル系樹
脂、ポリスチレン系樹脂又はABS系樹脂の少なくとも
1種類から選ばれた熱可塑性樹脂及びカーボンブラック
からなるIC包装用導電性樹脂組成物において、この導
電性樹脂組成物に、さらに、エチレン−α−オレフィン
共重合体樹脂を含有させることにより、該導電性樹脂組
成物から成るIC包装用の成形品において、成形品とI
C等との接触・摩耗が原因となるカーボンブラック等の
脱離によるIC等の汚染を著しく減少させたIC包装用
導電性樹脂組成物を提供しようとするものである。
SUMMARY OF THE INVENTION The present invention is intended to solve such a drawback and comprises a thermoplastic resin selected from at least one of polyphenylene ether resin, polystyrene resin or ABS resin and carbon black. In a conductive resin composition for IC packaging, the conductive resin composition further contains an ethylene-α-olefin copolymer resin to obtain a molded article for IC packaging made of the conductive resin composition. , Molded articles and I
It is an object of the present invention to provide a conductive resin composition for IC packaging in which contamination of IC and the like due to detachment of carbon black and the like caused by contact and abrasion with C and the like is significantly reduced.

【0007】[0007]

【課題を解決するための手段】すなわち、本発明の第1
の発明は、(A)ポリフェニレンエーテル系樹脂、ポリ
スチレン系樹脂又はABS系樹脂の少なくとも1種類か
ら選ばれた熱可塑性樹脂、(B)カーボンブラック及び
(C)エチレン−α−オレフィン共重合体樹脂からなる
IC包装用導電性樹脂組成物において、(a)前記
(A)熱可塑性樹脂100重量部に対し(B)カーボン
ブラック5〜50重量部を含有し、かつ、前記(A)熱
可塑性樹脂と(B)カーボンブラックの合計量100重
量部に対し、JIS−K−7215によるデユロメータ
A型表面硬度が90以下の(C)エチレン−α−オレフ
ィン共重合体樹脂1〜30重量部を含有してなり、か
つ、(b)導電性樹脂組成物の表面固有抵抗値が102
〜1010Ωであることを特徴とするIC包装用導電性樹
脂組成物である。
That is, the first aspect of the present invention
Is a thermoplastic resin selected from at least one of (A) polyphenylene ether resin, polystyrene resin or ABS resin, (B) carbon black and (C) ethylene-α-olefin copolymer resin. In a conductive resin composition for IC packaging, (a) contains 5 to 50 parts by weight of carbon black (B) per 100 parts by weight of the thermoplastic resin (A), and contains (A) the thermoplastic resin. (B) 1 to 30 parts by weight of (C) ethylene-α-olefin copolymer resin having a durometer A type surface hardness of 90 or less according to JIS-K-7215 is contained with respect to 100 parts by weight of the total amount of carbon black. And (b) the surface specific resistance value of the conductive resin composition is 10 2
The conductive resin composition for IC packaging is characterized by having a resistance of 10 to 10 10 Ω.

【0008】以下、本発明を更に詳細に説明する。本発
明においては、(A)ポリフェニレンエーテル系樹脂、
ポリスチレン系樹脂又はABS系樹脂の少なくとも1種
類から選ばれた熱可塑性樹脂が使用され、ポリフェニレ
ンエーテル系樹脂とはポリフェニレンエーテル樹脂とポ
リスチレン系樹脂を主成分とする樹脂をいい、ポリフェ
ニレンエーテル樹脂とポリスチレン系樹脂の合計量10
0重量部におけるポリフェニレンエーテル樹脂の含有量
は28〜86重量部が好ましく、28重量部未満ではポ
リフェニレンエーテル系樹脂としての十分な力学特性が
得られず、86重量部を越えると流動性の低下により成
形加工が困難となる。該ポリフェニレンエーテル樹脂と
は米国特許3383435号に記載されているホモポリ
マー或いは共重合体が示される。
The present invention will be described in more detail below. In the present invention, (A) polyphenylene ether resin,
A thermoplastic resin selected from at least one type of polystyrene-based resin or ABS-based resin is used, and the polyphenylene ether-based resin means a resin containing polyphenylene ether resin and polystyrene-based resin as main components, and polyphenylene ether resin and polystyrene-based resin. Total amount of resin 10
The content of the polyphenylene ether resin in 0 part by weight is preferably 28 to 86 parts by weight. If it is less than 28 parts by weight, sufficient mechanical properties as a polyphenylene ether resin cannot be obtained, and if it exceeds 86 parts by weight, fluidity is deteriorated. Molding becomes difficult. The polyphenylene ether resin is a homopolymer or copolymer described in US Pat. No. 3,383,435.

【0009】本発明で使用するポリスチレン系樹脂とは
一般のポリスチレン樹脂又は耐衝撃性ポリスチレン樹脂
及びこれらの混合物を主成分とするものをいい、ABS
系樹脂とはアクリルニトリル−ブタジエン−スチレンの
三成分を主体とした共重合体を主成分とするものをい
う。
The polystyrene resin used in the present invention is a general polystyrene resin or a high impact polystyrene resin and a resin containing a mixture thereof as a main component.
The system resin means a resin containing a copolymer mainly composed of acrylonitrile-butadiene-styrene as a main component.

【0010】本発明で使用する(C)カーボンブラック
は、ファーネスブラック、チャンネルブラック、アセチ
レンブラック等であり、好ましくは比表面積が大きく、
樹脂への添加量が少量で高度の導電性が得られるもので
ある。例えば,S.C.F.(Super Condu
ctive Furnace)、E.C.F.(Ele
ctric Conductive Furnac
e)、ケッチェンブラック(ライオン−AKZO社製商
品名)及びアセチレンブラックである。カーボンブラッ
クの添加量は、表面固有抵抗値が102 〜1010Ωとす
ることのできる添加量であり、かつ(A)熱可塑性樹脂
100重量部に対し(B)カーボンブラック5〜50重
量部が好ましい。添加量が5重量部未満では十分な導電
性が得られず表面固有抵抗値が上昇してしまい、また5
0重量部を越えると樹脂との均一分散性が悪化し、成形
加工が困難となり、かつ、機械的強度等の特性値が低下
してしまう。また、表面固有抵抗値が1010Ωを越える
と十分な帯電防止効果が得られず、102 Ω未満では、
導電性が良すぎて電磁誘導や静電誘導などにより起電力
が生じICを破壊する恐れがある。
The carbon black (C) used in the present invention is furnace black, channel black, acetylene black, etc., preferably having a large specific surface area,
High conductivity can be obtained with a small amount added to the resin. For example, S. C. F. (Super Condu
active Furnace), E.I. C. F. (Ele
ctric Conductive Furnac
e), Ketjen Black (trade name of Lion-AKZO) and acetylene black. The amount of carbon black added is such that the surface resistivity can be 10 2 to 10 10 Ω, and (B) 5 to 50 parts by weight of (B) carbon black per 100 parts by weight of the thermoplastic resin. Is preferred. If the addition amount is less than 5 parts by weight, sufficient conductivity cannot be obtained and the surface resistivity value increases.
If the amount exceeds 0 parts by weight, the uniform dispersibility with the resin deteriorates, the molding process becomes difficult, and the characteristic values such as mechanical strength decrease. If the surface resistivity exceeds 10 10 Ω, a sufficient antistatic effect cannot be obtained, and if it is less than 10 2 Ω,
The conductivity is too good, and electromotive force may be generated by electromagnetic induction or electrostatic induction, which may damage the IC.

【0011】本発明で使用する(C)エチレン−α−オ
レフィン共重合体樹脂は、エチレンとα−オレフィンを
共重合した樹脂をいい、エチレンと共重合するα−オレ
フィンとしては、ポロピレン、ブテンー1、ペンテンー
1、ヘキセンー1等があり、例えば、三井石油化学社、
「タフマーP」及び「タフマーA」等である。エチレン
−α−オレフィン共重合体樹脂はJIS−K−7215
で言うデユロメータA型表面硬度が90以下のものが好
ましく、メルトフローインデックス(JISK−721
0に準じ測定)は、190℃、荷重2.16kgの条件
で0.1g/10分以上であり、この数値未満ではポリ
フェニレンエーテル系樹脂、ポリスチレン系樹脂、AB
S系樹脂との混練が困難となり、良好な組成物が得られ
ない。エチレン−α−オレフィン共重合体樹脂の添加量
は、熱可塑性樹脂とカーボンブラックの合計量100重
量部に対して、1〜30重量部が好ましく、特に好まし
くは3〜25重量部である。添加量が1重量部未満では
その効果が不十分であり、30重量部を越えるとポリフ
ェニレンエーテル系樹脂、ポリスチレン系樹脂、ABS
系樹脂中に均一に分散させることが困難となる。
The ethylene-α-olefin copolymer resin (C) used in the present invention is a resin in which ethylene and α-olefin are copolymerized, and as the α-olefin copolymerized with ethylene, poroprene and butene-1 are used. , Pentene-1, hexene-1, etc., for example, Mitsui Petrochemical Company,
Examples are "Tuffmer P" and "Tuffmer A". The ethylene-α-olefin copolymer resin is JIS-K-7215.
Durometer A-type surface hardness of 90 or less is preferable, and the melt flow index (JISK-721
0) is 0.1 g / 10 minutes or more under the conditions of 190 ° C. and a load of 2.16 kg. Below this value, polyphenylene ether resin, polystyrene resin, AB
Kneading with the S-based resin becomes difficult, and a good composition cannot be obtained. The addition amount of the ethylene-α-olefin copolymer resin is preferably 1 to 30 parts by weight, and particularly preferably 3 to 25 parts by weight, based on 100 parts by weight of the total amount of the thermoplastic resin and the carbon black. If the addition amount is less than 1 part by weight, the effect is insufficient, and if it exceeds 30 parts by weight, polyphenylene ether resin, polystyrene resin, ABS are used.
It becomes difficult to disperse the resin uniformly in the resin.

【0012】本発明の導電性樹脂組成物は、十分な成形
加工性を維持するために、表面固有抵抗値が102 〜1
10Ωとなるようにカーボンブラックを充填した場合、
メルトフローインデックス(JIS−K−7210に準
じ測定)が、ポリフェニレンエーテル系樹脂に充填した
場合、230℃、荷重10kgの条件で、ポリスチレン
系樹脂に充填した場合、200℃、荷重5kgの条件
で、ABS系樹脂に充填した場合、220℃、荷重10
kgの条件で、それぞれ、0.1g/10分以上であ
る。
The conductive resin composition of the present invention has a surface resistivity of 10 2 to 1 in order to maintain sufficient moldability.
When carbon black is filled to 0 10 Ω,
Melt flow index (measured according to JIS-K-7210) is 230 ° C. under a load of 10 kg when filled in a polyphenylene ether resin, and 200 ° C. under a load of 5 kg when filled in a polystyrene resin. When filled with ABS resin, 220 ° C, load 10
Under the condition of kg, each is 0.1 g / 10 minutes or more.

【0013】更に、本発明の導電性樹脂組成物には、必
要に応じて流動特性を改善するための滑剤、可塑剤、加
工助剤、成形品の力学特性を改善するための補強剤など
の各種添加剤や他の樹脂成分を添加することが可能であ
る。本発明において、樹脂等各種原材料を混練、ペレッ
ト化するにはバンバリーミキサー、押出機等の公知の方
法を用いることが可能である。
Further, in the conductive resin composition of the present invention, a lubricant, a plasticizer, a processing aid, a reinforcing agent for improving the mechanical properties of a molded article, etc. for improving the fluidity properties may be added, if necessary. Various additives and other resin components can be added. In the present invention, a known method such as a Banbury mixer or an extruder can be used for kneading and pelletizing various raw materials such as resin.

【0014】[0014]

【実施例】以下本発明を実施例によりさらに詳細に説明
する。 実施例1〜4 表1に示す原料組成割合にて原料を各々計量し、高速混
合機より均一に混合した後、φ45mmベント式二軸押
出機を用いて混練し、ストランドカット法によりペレッ
ト化した。次にペレット化した樹脂組成物をサンプルM
はφ65mm押出機(L/D=28)を用い500mm
幅のTダイにより厚さ500μmのシート状に成形した
もの、サンプルNは、インジェクション成形機(100
t)により厚さ1mm×120mm角のプレート状及び
引張測定用試験片形状に成形したものを評価用のサンプ
ルとした。評価結果を表3及び表4に示す。各実施例に
おいては、カーボンブラックの脱落は無かった。
EXAMPLES The present invention will now be described in more detail with reference to examples. Examples 1 to 4 Raw materials were weighed at the raw material composition ratios shown in Table 1, uniformly mixed by a high-speed mixer, then kneaded using a φ45 mm vent type twin-screw extruder, and pelletized by a strand cut method. . Next, the pelletized resin composition is used as sample M.
Is a φ65 mm extruder (L / D = 28) and is 500 mm
What was molded into a sheet shape with a thickness of 500 μm by a T-die having a width, Sample N was an injection molding machine (100
A sample for evaluation was formed by t) in the form of a plate having a thickness of 1 mm × 120 mm square and a test piece for tensile measurement. The evaluation results are shown in Tables 3 and 4. In each example, the carbon black did not fall off.

【0015】比較例1〜4 実施例1と同様にして、表2に示す原料組成割合にて原
料を各々計量し、高速混合機より均一に混合した後、φ
45mmベント式二軸押出機を用いて混練し、ストラン
ドカット法によりペレット化した。次にペレット化した
樹脂組成物にてサンプルM及びサンプルNを作成し評価
した。評価結果を表3及び表4に示す。各比較例におい
ては、カーボンブラックの脱落が確認された。
Comparative Examples 1 to 4 In the same manner as in Example 1, the raw materials were weighed at the raw material composition ratios shown in Table 2, uniformly mixed by a high speed mixer, and then φ
The mixture was kneaded using a 45 mm vent type twin-screw extruder and pelletized by a strand cut method. Next, the pelletized resin composition was used to prepare and evaluate Samples M and N. The evaluation results are shown in Tables 3 and 4. In each comparative example, it was confirmed that the carbon black had fallen off.

【0016】[0016]

【表1】 [Table 1]

【0017】[0017]

【表2】 [Table 2]

【0018】[0018]

【表3】 [Table 3]

【0019】[0019]

【表4】 [Table 4]

【0020】尚、各評価は次に示す方法によって行っ
た。 (1)表面固有抵抗 サンプルM及びNともにロレスター表面抵抗計(三菱油
化社製)により電極間を10mmとしサンプル中任意の
10点を測定し、その対数平均値を表面固有抵抗値とし
た。 (2)破断点強度、引張弾性率 JIS−K−7113に準拠しサンプルMについては2
号形試験片、サンプルNについては1号形試験片を引張
速度10mm/minで測定した。
Each evaluation was performed by the following method. (1) Surface specific resistance For both samples M and N, the distance between the electrodes was set to 10 mm using a Lorester surface resistance meter (manufactured by Mitsubishi Petrochemical Co., Ltd.), and arbitrary 10 points in the sample were measured, and the logarithmic average value thereof was taken as the surface specific resistance. (2) Strength at Break, Tensile Elastic Modulus According to JIS-K-7113, Sample M is 2
For the No. 1 type test piece and the sample N, the No. 1 type test piece was measured at a tensile speed of 10 mm / min.

【0021】(3)カーボン脱落の有無 各シート及びプレートサンプルの表面にQFP14mm
×20mm/64pinのICを100gの荷重で押し
付け、ストローク15mmで100往復させ、その後I
Cのリード部をマイクロスコープで観察した。リード部
におけるカーボンブラック等黒色の付着物の有無で評価
した。(4)MFI各実施例及び比較例のペレットにつ
いてJIS−7210に準拠し測定を行った。
(3) Presence or absence of carbon loss QFP 14 mm on the surface of each sheet and plate sample
An IC of × 20mm / 64pin is pressed with a load of 100g, and a stroke of 15mm is made to reciprocate 100 times.
The lead portion of C was observed with a microscope. It was evaluated by the presence or absence of black deposits such as carbon black on the lead portion. (4) MFI The pellets of Examples and Comparative Examples were measured according to JIS-7210.

【0022】[0022]

【発明の効果】以上説明したとおり、(A)ポリフェニ
レンエーテル系樹脂、ポリスチレン系樹脂又はABS系
樹脂の少なくとも1種類から選ばれた熱可塑性樹脂及び
カーボンブラックからなるIC包装用導電性樹脂組成物
において、この導電性樹脂組成物に、さらに、エチレン
−α−オレフィン共重合体樹脂を含有させることによ
り、IC等と接触時の摩耗によるカーボンブラックの脱
離が原因となるIC等の汚染を著しく減少させた導電性
樹脂組成物を得ることが可能となる。
As described above, in the conductive resin composition for IC packaging, which comprises (A) a thermoplastic resin selected from at least one kind of polyphenylene ether resin, polystyrene resin or ABS resin, and carbon black. By further adding an ethylene-α-olefin copolymer resin to this conductive resin composition, the contamination of IC or the like caused by the desorption of carbon black due to abrasion at the time of contact with IC or the like is significantly reduced. It is possible to obtain the conductive resin composition.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 H01L 23/29 23/31 //(C08L 71/12 23:08) ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 6 Identification code Internal reference number FI technical display area H01L 23/29 23/31 // (C08L 71/12 23:08)

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 (A)ポリフェニレンエーテル系樹脂、
ポリスチレン系樹脂又はABS系樹脂の少なくとも1種
類から選ばれた熱可塑性樹脂、(B)カーボンブラック
及び(C)エチレン−α−オレフィン共重合体樹脂から
なるIC包装用導電性樹脂組成物において、(a)前記
(A)熱可塑性樹脂100重量部に対し(B)カーボン
ブラック5〜50重量部を含有し、かつ、前記(A)熱
可塑性樹脂と(B)カーボンブラックの合計量100重
量部に対し、JIS−K−7215によるデユロメータ
A型表面硬度が90以下の(C)エチレン−α−オレフ
ィン共重合体樹脂1〜30重量部を含有してなり、か
つ、(b)導電性樹脂組成物の表面固有抵抗値が102
〜1010Ωであることを特徴とするIC包装用導電性樹
脂組成物。
1. A polyphenylene ether resin (A),
In a conductive resin composition for IC packaging, which comprises a thermoplastic resin selected from at least one type of polystyrene resin or ABS resin, (B) carbon black and (C) ethylene-α-olefin copolymer resin, a) 5 to 50 parts by weight of (B) carbon black is contained per 100 parts by weight of the (A) thermoplastic resin, and the total amount of the (A) thermoplastic resin and (B) carbon black is 100 parts by weight. On the other hand, it contains 1 to 30 parts by weight of (C) ethylene-α-olefin copolymer resin having a Durometer A type surface hardness of 90 or less according to JIS-K-7215, and (b) a conductive resin composition. Surface resistivity of 10 2
A conductive resin composition for IC packaging, which has a resistance of 10 to 10 10 Ω.
JP01068695A 1995-01-26 1995-01-26 Conductive resin composition Expired - Lifetime JP3308748B2 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
JP01068695A JP3308748B2 (en) 1995-01-26 1995-01-26 Conductive resin composition
US08/834,297 US5707699A (en) 1995-01-26 1997-04-15 Electroconductive resin composition, sheet, molded product and container
US08/917,606 US5876632A (en) 1995-01-26 1997-08-26 Electroconductive resin composition, sheet, molded product and container
US09/199,489 US5955164A (en) 1995-01-26 1998-11-25 Electroconductive resin composition, sheet, molded product and container

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP01068695A JP3308748B2 (en) 1995-01-26 1995-01-26 Conductive resin composition

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2002101010A Division JP3721340B2 (en) 2002-04-03 2002-04-03 Conductive resin composition

Publications (2)

Publication Number Publication Date
JPH08198999A true JPH08198999A (en) 1996-08-06
JP3308748B2 JP3308748B2 (en) 2002-07-29

Family

ID=11757162

Family Applications (1)

Application Number Title Priority Date Filing Date
JP01068695A Expired - Lifetime JP3308748B2 (en) 1995-01-26 1995-01-26 Conductive resin composition

Country Status (1)

Country Link
JP (1) JP3308748B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2011219557A (en) * 2010-04-06 2011-11-04 Nippon A&L Inc Thermoplastic resin composition and molding

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2011219557A (en) * 2010-04-06 2011-11-04 Nippon A&L Inc Thermoplastic resin composition and molding

Also Published As

Publication number Publication date
JP3308748B2 (en) 2002-07-29

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