JPH0718152A - Electrostatic charge-substaining composite material - Google Patents
Electrostatic charge-substaining composite materialInfo
- Publication number
- JPH0718152A JPH0718152A JP16104093A JP16104093A JPH0718152A JP H0718152 A JPH0718152 A JP H0718152A JP 16104093 A JP16104093 A JP 16104093A JP 16104093 A JP16104093 A JP 16104093A JP H0718152 A JPH0718152 A JP H0718152A
- Authority
- JP
- Japan
- Prior art keywords
- potential
- composite material
- electrostatic charge
- weight
- present
- 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
Links
- 239000002131 composite material Substances 0.000 title claims abstract description 12
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims abstract description 18
- 239000002245 particle Substances 0.000 claims abstract description 13
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 claims abstract description 11
- 239000000835 fiber Substances 0.000 claims abstract description 10
- 229920000049 Carbon (fiber) Polymers 0.000 claims abstract description 9
- 239000004917 carbon fiber Substances 0.000 claims abstract description 9
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims description 7
- 239000000203 mixture Substances 0.000 claims description 6
- 229920000515 polycarbonate Polymers 0.000 claims description 2
- 239000004417 polycarbonate Substances 0.000 claims description 2
- 239000000463 material Substances 0.000 abstract description 12
- 229920005668 polycarbonate resin Polymers 0.000 abstract description 11
- 239000004431 polycarbonate resin Substances 0.000 abstract description 11
- 230000007246 mechanism Effects 0.000 abstract description 5
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 13
- 230000007423 decrease Effects 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 239000011787 zinc oxide Substances 0.000 description 5
- 238000007796 conventional method Methods 0.000 description 4
- 230000005611 electricity Effects 0.000 description 4
- 239000000945 filler Substances 0.000 description 4
- 238000004898 kneading Methods 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- 230000003068 static effect Effects 0.000 description 4
- 230000007257 malfunction Effects 0.000 description 3
- 229920003051 synthetic elastomer Polymers 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- XECAHXYUAAWDEL-UHFFFAOYSA-N acrylonitrile butadiene styrene Chemical compound C=CC=C.C=CC#N.C=CC1=CC=CC=C1 XECAHXYUAAWDEL-UHFFFAOYSA-N 0.000 description 2
- 239000004676 acrylonitrile butadiene styrene Substances 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000003063 flame retardant Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 239000011342 resin composition Substances 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- 229920005992 thermoplastic resin Polymers 0.000 description 2
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
- ODJUOZPKKHIEOZ-UHFFFAOYSA-N 4-[2-(4-hydroxy-3,5-dimethylphenyl)propan-2-yl]-2,6-dimethylphenol Chemical compound CC1=C(O)C(C)=CC(C(C)(C)C=2C=C(C)C(O)=C(C)C=2)=C1 ODJUOZPKKHIEOZ-UHFFFAOYSA-N 0.000 description 1
- 229920000298 Cellophane Polymers 0.000 description 1
- 241001590997 Moolgarda engeli Species 0.000 description 1
- 239000008411 PCM 4 Substances 0.000 description 1
- 239000006087 Silane Coupling Agent Substances 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 150000004650 carbonic acid diesters Chemical class 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 239000011231 conductive filler Substances 0.000 description 1
- 229920001940 conductive polymer Polymers 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- ROORDVPLFPIABK-UHFFFAOYSA-N diphenyl carbonate Chemical compound C=1C=CC=CC=1OC(=O)OC1=CC=CC=C1 ROORDVPLFPIABK-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000012766 organic filler Substances 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 238000007747 plating Methods 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000012756 surface treatment agent Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は新規な複合材料、さらに
詳しくは、帯電電位が瞬時にある一定電位まで低下し、
それ以降はその電位が維持されるか、あるいは徐々に低
下するという特性を有するとともに、成形性、二次加工
性に優れ、IC使用機構の部材や静電気防止部材などに
好適に用いられる複合材料に関するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a novel composite material, more specifically, the charging potential is instantaneously lowered to a certain constant potential,
After that, the present invention relates to a composite material that has characteristics that its potential is maintained or gradually decreases, and that is excellent in moldability and secondary workability, and that is suitable for use as a member of an IC using mechanism or an antistatic member. It is a thing.
【0002】[0002]
【従来の技術】従来、プラスチックに帯電防止性を付与
させる方法としては、例えば帯電防止材料として、金属
系導電材やカーボンブラックを中心とする電子電導型充
填剤や、界面活性剤のようなイオン電導型充填剤を配合
する方法、あるいは樹脂自身に導電性をもたせる方法
(導電性ポリマーの使用)などが知られている。そし
て、これらの方法はいずれも、外部からの電気刺激(例
えば摩擦による静電気)を受けると、瞬間的に抵抗値を
低下し(除電され)、帯電電位を零に近づけることを目
的とするものである。2. Description of the Related Art Conventionally, as a method of imparting antistatic properties to plastics, for example, as an antistatic material, an electroconductive filler such as a metal-based conductive material or carbon black, or an ion such as a surfactant is used. A method of blending a conductive filler, a method of making the resin itself conductive (using a conductive polymer), and the like are known. When any of these methods receives an electrical stimulus from outside (for example, static electricity due to friction), the resistance value is instantaneously reduced (charge elimination), and the charge potential is made to approach zero. is there.
【0003】しかしながら、このような従来の方法によ
り帯電防止性が付与されたプラスチックは、電気抵抗の
減少、すなわち帯電防止効果はあっても、例えばICの
ハウジングやIC基板などに使用すると、このICの電
気的破壊や誤動作をもたらすことがあるなどの問題が生
じ、このような問題を解決することが大きな課題となっ
ている。However, even if the plastic to which the antistatic property is imparted by such a conventional method has a reduced electric resistance, that is, an antistatic effect, when it is used for an IC housing or an IC substrate, for example, this IC Problems such as electrical breakdown and malfunction may occur, and solving such problems is a major issue.
【0004】[0004]
【発明が解決しようとする課題】本発明は、このような
事情のもとで、特に静電気発生によるIC機構の電気的
破壊や誤動作を防止することのできる帯電性能が制御さ
れた複合材料を提供することを目的としてなされたもの
である。Under the circumstances, the present invention provides a composite material with controlled charging performance which can prevent electrical breakdown or malfunction of an IC mechanism due to generation of static electricity. It was made for the purpose of doing.
【0005】[0005]
【課題を解決するための手段】本発明者らは、帯電性の
制御された複合材料を開発すべく鋭意研究を重ねた結
果、特定の熱可塑性樹脂に、特定の粒径の酸化亜鉛粉末
及び特定の繊維長の炭素繊維をそれぞれ所定の割合で配
合した樹脂組成物が、帯電電位が瞬時にある一定電位ま
で低下し、それ以降はその電位が維持されるか、あるい
は徐々に低下するという特性を有し、しかも成形性及び
二次加工性も良好であることを見出し、この知見に基づ
いて本発明を完成するに至った。DISCLOSURE OF THE INVENTION As a result of intensive studies to develop a composite material having a controlled charging property, the present inventors have found that a specific thermoplastic resin can contain zinc oxide powder of a specific particle size and A resin composition in which carbon fibers each having a specific fiber length are mixed at a predetermined ratio, the charging potential is instantly reduced to a certain constant potential, and thereafter the potential is maintained or gradually lowered. In addition, it was found that the moldability and the secondary workability are good, and the present invention has been completed based on this finding.
【0006】すなわち、本発明は、少なくとも、(A)
ABS樹脂又はポリカーボネート樹脂あるいはそれらの
混合物55〜92重量%、(B)平均粒径0.1〜10
μmの酸化亜鉛粉末5〜30重量%及び(C)繊維長2
〜8mmの炭素繊維3〜15重量%から成る帯電持続性
複合材料を提供するものである。That is, the present invention is at least (A)
ABS resin or polycarbonate resin or a mixture thereof 55 to 92% by weight, (B) average particle size 0.1 to 10
5-30% by weight of zinc oxide powder of μm and (C) fiber length 2
The present invention provides a charge-sustaining composite material comprising 3 to 15% by weight of carbon fiber having a diameter of 8 mm.
【0007】本発明組成物においては、(A)成分のマ
トリックス樹脂としてABS樹脂やポリカーボネート樹
脂が用いられる。該ABS樹脂(アクリロニトリル‐ブ
タジエン‐スチレン共重合体)としては、種々の製法に
より得られたものがあるが、いずれのものも使用するこ
とができる。In the composition of the present invention, an ABS resin or a polycarbonate resin is used as the matrix resin of the component (A). As the ABS resin (acrylonitrile-butadiene-styrene copolymer), there are resins obtained by various production methods, but any of them can be used.
【0008】また、ポリカーボネート樹脂としては、
2,2‐ビス(4‐ヒドロキシフェニル)プロパン(ビ
スフェノールA)とホスゲンとを反応させるホスゲン法
や、ビスフェノールAとジフェニルカーボネートなどの
炭酸ジエステルとを反応させるエステル交換法などによ
り得られるビスフェノールA系ポリカーボネート樹脂が
好ましく用いられる。また、ビスフェノールAの一部を
2,2‐ビス(4‐ヒドロキシ‐3,5‐ジメチルフェ
ニル)プロパンや2,2‐ビス(4‐ヒドロキシ‐3,
5‐ジブロモフェニル)プロパンなどで置換した変性ビ
スフェノールA系ポリカーボネート樹脂や難燃化ビスフ
ェノールA系ポリカーボネート樹脂なども用いることが
できる。Further, as the polycarbonate resin,
Bisphenol A-based polycarbonate obtained by a phosgene method in which 2,2-bis (4-hydroxyphenyl) propane (bisphenol A) is reacted with phosgene, or a transesterification method in which bisphenol A is reacted with a carbonic acid diester such as diphenyl carbonate Resin is preferably used. Moreover, a part of bisphenol A is 2,2-bis (4-hydroxy-3,5-dimethylphenyl) propane or 2,2-bis (4-hydroxy-3,3).
A modified bisphenol A-based polycarbonate resin substituted with 5-dibromophenyl) propane or a flame-retardant bisphenol A-based polycarbonate resin can also be used.
【0009】本発明材料においては、(A)成分とし
て、ABS樹脂や、ポリカーボネート樹脂を単独で用い
てもよく、あるいはABS樹脂とポリカーボネート樹脂
とを混合して用いてもよい。また、本発明材料における
(A)成分の含有量は55〜92重量%の範囲にあるこ
とが必要である。この含有量が55重量%未満では帯電
電位の低下が過剰になるとともに、外観、塗装性及び成
形性の劣ったものとなるし、92重量%を超えると当初
の帯電電位の低下が起りにくくなる。In the material of the present invention, as the component (A), an ABS resin or a polycarbonate resin may be used alone, or the ABS resin and the polycarbonate resin may be mixed and used. The content of the component (A) in the material of the present invention needs to be in the range of 55 to 92% by weight. If this content is less than 55% by weight, the charging potential will be excessively lowered, and the appearance, paintability and moldability will be poor, and if it exceeds 92% by weight, the initial reduction of the charging potential will be less likely to occur. .
【0010】本発明材料においては、(B)成分とし
て、平均粒径0.1〜10μmの酸化亜鉛粉末が用いら
れる。この酸化亜鉛粉末の平均粒径が0.1μm未満で
は当初の帯電電位が低下しにくい上、粒子の凝集を起こ
しやすく、かつ外観も悪くなる。一方、平均粒径が10
μmを超えると帯電電位の低下が過剰になる。In the material of the present invention, zinc oxide powder having an average particle size of 0.1 to 10 μm is used as the component (B). When the average particle size of the zinc oxide powder is less than 0.1 μm, the initial charging potential is unlikely to be lowered, and the particles are apt to aggregate, and the appearance is also deteriorated. On the other hand, the average particle size is 10
If it exceeds μm, the charging potential is excessively lowered.
【0011】本発明材料における(B)成分の含有量は
5〜30重量%の範囲にあることが必要である。この含
有量が5重量%未満では当初の帯電電位が低下しにくい
し、30重量%を超えると外観、塗装性及び成形性が低
下する。The content of the component (B) in the material of the present invention needs to be in the range of 5 to 30% by weight. If this content is less than 5% by weight, the initial charging potential is unlikely to decrease, and if it exceeds 30% by weight, the appearance, paintability and moldability deteriorate.
【0012】本発明材料においては、(C)成分として
繊維長2〜8mmの炭素繊維が用いられる。この炭素繊
維の種類については特に制限はなく、ポリアクリロニト
リル系、ピッチ系のいずれも用いることができる。この
炭素繊維の繊維長が2mm未満では当初の帯電電位の低
下が起りにくいし、5mmを超えると帯電電位の低下が
過剰になる上に、外観、塗装性及び成形性が悪くなる。In the material of the present invention, carbon fiber having a fiber length of 2 to 8 mm is used as the component (C). The type of carbon fiber is not particularly limited, and either polyacrylonitrile-based or pitch-based can be used. If the fiber length of this carbon fiber is less than 2 mm, the initial decrease in the charging potential is unlikely to occur, and if it exceeds 5 mm, the decrease in the charging potential becomes excessive and the appearance, paintability and moldability deteriorate.
【0013】本発明材料における(C)成分の含有量は
3〜15重量%の範囲にあることが必要である。この含
有量が3重量%未満では当初の帯電電位の低下が起りに
くいし、15重量%を超えると帯電電位の低下が過剰に
なる上に、外観、塗装性及び成分性が悪くなる。The content of the component (C) in the material of the present invention must be in the range of 3 to 15% by weight. If the content is less than 3% by weight, the initial decrease in the charging potential is unlikely to occur, and if it exceeds 15% by weight, the decrease in the charging potential becomes excessive, and the appearance, paintability and composition are deteriorated.
【0014】本発明材料においては、前記(B)成分の
酸化亜鉛粉末や(C)成分の炭素繊維は、所望に応じ、
適当な表面処理剤で表面処理を施して用いてもよい。こ
の表面処理剤としては、例えばシラン系カップリング
剤、チタネート系カップリング剤、シリカ粉末、シリコ
ーンオイル、高級脂肪酸、高級アルコール、ワックス類
などを挙げることができる。In the material of the present invention, the zinc oxide powder as the component (B) and the carbon fiber as the component (C) may be, if desired,
You may use, after surface-treating with a suitable surface treating agent. Examples of the surface treatment agent include silane coupling agents, titanate coupling agents, silica powder, silicone oil, higher fatty acids, higher alcohols and waxes.
【0015】また、本発明材料には、本発明の目的がそ
こなわれない範囲で、所望に応じ他の熱可塑性樹脂や他
の金属フィラー、硫酸バリウム、炭酸カルシウム、クレ
ー、タルク、マイカなどの無機質フィラーや有機質フィ
ラー、さらには樹脂組成物に通常用いられている各種添
加剤、例えば滑剤、着色剤、安定剤、酸化防止剤、紫外
線吸収剤、難燃剤、可塑剤などを配合することができ
る。Further, in the material of the present invention, if desired, other thermoplastic resins, other metal fillers, barium sulfate, calcium carbonate, clay, talc, mica, etc. may be used as long as the object of the present invention is not impaired. Inorganic fillers and organic fillers, as well as various additives commonly used in resin compositions, such as lubricants, colorants, stabilizers, antioxidants, ultraviolet absorbers, flame retardants, plasticizers and the like can be blended. .
【0016】本発明の複合材料の調製方法は慣用の方法
に従って行うことができ、例えば前記(A)成分、
(B)成分、(C)成分及び必要に応じて用いられる各
種添加成分を、常法に従って溶融混練し、複合化するこ
とによって調製することができる。溶融混練は、例えば
ヘンシェルミキサー、単軸又は二軸押出機、バンバリー
ミキサー、ロールなどを用いる方法や、その他常法によ
り行うことができるが、特にヘンシェルミキサー、押出
機、バンバリーミキサーを用いて行うことが好ましい。The composite material of the present invention can be prepared by a conventional method. For example, the above-mentioned component (A),
It can be prepared by melt-kneading the component (B), the component (C), and various additives used as necessary according to a conventional method to form a composite. Melt kneading can be performed by, for example, a method using a Henschel mixer, a single-screw or twin-screw extruder, a Banbury mixer, a roll or the like, and other conventional methods, but particularly, using a Henschel mixer, an extruder, a Banbury mixer. Is preferred.
【0017】[0017]
【発明の効果】本発明の複合材料は、帯電電位を瞬時に
ある一定電位まで低下させ、それ以降はその電位を維持
するか、あるいは徐々に低下させる特性を有しており、
IC使用機構の部材(例えばハウジング、基板など)や
静電気発生防止部材(例えばハウジングなど)などに好
適に用いられる。特にIC使用機構の部材に用いること
により、静電気発生によるICの電気的破壊や誤動作を
有効に防止することができる。INDUSTRIAL APPLICABILITY The composite material of the present invention has the characteristic that the charging potential is instantly lowered to a certain constant potential, and thereafter the potential is maintained or gradually lowered.
It is preferably used as a member of an IC using mechanism (for example, a housing, a substrate, etc.), a static electricity generation preventing member (for example, a housing, etc.) and the like. In particular, when it is used as a member of an IC using mechanism, it is possible to effectively prevent electrical damage or malfunction of the IC due to generation of static electricity.
【0018】また、成形性に優れるとともに、めっき、
塗装、印刷などの二次加工性にも優れており、大型成形
品や精密部品などの素材としても好適に用いられ、外観
が美麗な製品を与える。In addition to excellent moldability, plating,
It is also excellent in secondary workability such as painting and printing, and is suitable for use as a material for large-scale molded products and precision parts, and gives a product with a beautiful appearance.
【0019】[0019]
【実施例】次に実施例により本発明をさらに詳細に説明
するが、本発明はこれらの例によってなんら限定される
ものではない。EXAMPLES The present invention will be described in more detail by way of examples, which should not be construed as limiting the invention thereto.
【0020】なお、組成物の特性は次のようにして評価
した。 (1)帯電電位(kv) 試供板(150×150×3mm)中央部に、静電気発
生機にて電圧25kvを1秒毎に2分間引加した。印加
終了後、印加時(初期)、10秒間、30秒間、1分
後、10分後の電位を静電気測定器にて測定し、帯電電
圧(kv)とした。The characteristics of the composition were evaluated as follows. (1) Charging potential (kv) A voltage of 25 kv was applied to the center of the sample plate (150 x 150 x 3 mm) every second for 2 minutes with an electrostatic generator. After the completion of application, at the time of application (initial stage), 10 seconds, 30 seconds, 1 minute, and 10 minutes later, the potential was measured by an electrostatic measurement device and defined as a charging voltage (kv).
【0021】(2)塗装性 (イ)密着性 テストピース(100×100×3.2mm)に化学塗
料[カシュー(株)製、マイクロン3000]を吹付
け、80℃で20分間焼付け、乾燥したのち、1mm角
の碁盤目を鋭利なカッターで100ケ作製し、セロテー
プで剥離し、x/100値を求めた(x:碁盤目の残
数)。(2) Coating property (a) Adhesion property A chemical paint [Micron 3000, manufactured by Cashew Co., Ltd.] was sprayed on a test piece (100 × 100 × 3.2 mm), baked at 80 ° C. for 20 minutes, and dried. After that, 100 squares of 1 mm square were made with a sharp cutter and peeled off with cellophane tape, and x / 100 value was obtained (x: remaining number of squares).
【0022】(ロ)外観 塗装後の外観を目視観察し、次の基準で評価した。 ○:美麗 △:一部充填剤の凹凸あり ×:著しい充填剤の凹凸あり(B) Appearance The appearance after coating was visually observed and evaluated according to the following criteria. ◯: Beautiful Δ: Partially unevenness of filler X: Significant unevenness of filler
【0023】(3)成形性 ABS樹脂系の場合は200℃、5kg荷重の条件でM
I(g/10分)を求め、また、ポリカーボネート樹脂
系の場合は275℃、2.16kg荷重の条件でMI
(g/10分)を求めた。(3) Moldability In the case of ABS resin system, M under the condition of 200 ° C. and 5 kg load
I (g / 10 minutes) was calculated, and in the case of polycarbonate resin system, MI under the conditions of 275 ° C. and 2.16 kg load.
(G / 10 minutes) was determined.
【0024】また、複合材料の調製に使用した原材料を
次に示す。 (1)ABS樹脂 ABS−1:日本合成ゴム(株)製、JSR−21 ABS−2:日本合成ゴム(株)製、JSR−35 ABS−3:日本合成ゴム(株)製、JSR−38The raw materials used for preparing the composite material are shown below. (1) ABS resin ABS-1: manufactured by Japan Synthetic Rubber Co., Ltd., JSR-21 ABS-2: manufactured by Japan Synthetic Rubber Co., Ltd., JSR-35 ABS-3: manufactured by Japan Synthetic Rubber Co., Ltd., JSR-38
【0025】(2)ポリカーボネート樹脂 PC−1:出光石油化学(株)製、A−2200 PC−2:出光石油化学(株)製、A−2500(2) Polycarbonate resin PC-1: A-2200 manufactured by Idemitsu Petrochemical Co., Ltd. PC-2: A-2500 manufactured by Idemitsu Petrochemical Co., Ltd.
【0026】(3)酸化亜鉛粉末 ZnO−1:白水化学(株)製、導電ZnO、平均粒径
3μm ZnO−2:白水化学(株)製、導電ZnO、平均粒径
0.05μm ZnO−3:白水化学(株)製、導電ZnO、平均粒径
8μm ZnO−4:白水化学(株)製、導電ZnO、平均粒径
15μm ZnO−5:白水化学(株)製、汎用ZnO、平均粒径
3μm(3) Zinc oxide powder ZnO-1: manufactured by Shiramizu Chemical Co., Ltd., conductive ZnO, average particle size 3 μm ZnO-2: manufactured by Shiramizu Chemical Co., conductive ZnO, average particle size 0.05 μm ZnO-3 : Shiramizu Chemical Co., Ltd., conductive ZnO, average particle size 8 μm ZnO-4: Shiramizu Chemical Co., Ltd., conductive ZnO, average particle size 15 μm ZnO-5: Shiramizu Chemical Co., general-purpose ZnO, average particle size 3 μm
【0027】(4)炭素繊維 CF−1:三菱化成(株)製、繊維長3mm CF−2:三菱化成(株)製、繊維長1mm CF−3:三菱化成(株)製、繊維長6mm CF−4:三菱化成(株)製、繊維長10mm(4) Carbon Fiber CF-1: Mitsubishi Kasei Co., Ltd., fiber length 3 mm CF-2: Mitsubishi Kasei Co., Ltd., fiber length 1 mm CF-3: Mitsubishi Kasei Co., Ltd., fiber length 6 mm CF-4: manufactured by Mitsubishi Kasei Co., Ltd., fiber length 10 mm
【0028】実施例1〜27、比較例1〜10 表1及び表3に示す配合組成を二軸押出機[PCM−4
5、池貝鉄工(株)製]にて溶融混練し、ペレットを作
製して評価した。なお、ABS系材料の場合は溶融混練
温度を210〜220℃とし、ポリカーボネート樹脂系
材料の場合は、溶融混練温度を260〜280℃とし
た。Examples 1 to 27, Comparative Examples 1 to 10 The compounding compositions shown in Tables 1 and 3 were used as twin screw extruders [PCM-4.
5, manufactured by Ikegai Tekko Co., Ltd.] and melt-kneaded to prepare pellets for evaluation. The melt-kneading temperature was set to 210 to 220 ° C in the case of the ABS material, and the melt-kneading temperature was set to 260 to 280 ° C in the case of the polycarbonate resin material.
【0029】評価結果を表2及び表4に示す。The evaluation results are shown in Tables 2 and 4.
【0030】[0030]
【表1】 [Table 1]
【0031】[0031]
【表2】 [Table 2]
【0032】[0032]
【表3】 [Table 3]
【0033】[0033]
【表4】 [Table 4]
───────────────────────────────────────────────────── フロントページの続き (72)発明者 大川 秀夫 東京都千代田区神田和泉町1番地277 カ ルプ工業株式会社内 ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Inventor Hideo Okawa 1 277 Izumicho, Kanda, Chiyoda-ku, Tokyo Inside Calup Industry Co., Ltd.
Claims (1)
あるいはそれらの混合物樹脂55〜92重量%、(B)
平均粒径0.1〜10μmの酸化亜鉛粉末5〜30重量
%及び(C)繊維長2〜8mmの炭素繊維3〜15重量
%から成る帯電持続性複合材料。1. (A) ABS resin or polycarbonate or 55 to 92% by weight of a mixture thereof, (B)
A charge-sustaining composite material comprising 5 to 30% by weight of zinc oxide powder having an average particle size of 0.1 to 10 μm and (C) 3 to 15% by weight of carbon fiber having a fiber length of 2 to 8 mm.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP16104093A JPH0718152A (en) | 1993-06-30 | 1993-06-30 | Electrostatic charge-substaining composite material |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP16104093A JPH0718152A (en) | 1993-06-30 | 1993-06-30 | Electrostatic charge-substaining composite material |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH0718152A true JPH0718152A (en) | 1995-01-20 |
Family
ID=15727458
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP16104093A Pending JPH0718152A (en) | 1993-06-30 | 1993-06-30 | Electrostatic charge-substaining composite material |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0718152A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2002531673A (en) * | 1998-12-08 | 2002-09-24 | バイエル アクチェンゲゼルシャフト | Polycarbonate molding composition with improved mechanical properties |
| JP2016204480A (en) * | 2015-04-20 | 2016-12-08 | 帝人株式会社 | Polycarbonate resin composition |
-
1993
- 1993-06-30 JP JP16104093A patent/JPH0718152A/en active Pending
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2002531673A (en) * | 1998-12-08 | 2002-09-24 | バイエル アクチェンゲゼルシャフト | Polycarbonate molding composition with improved mechanical properties |
| JP2011094153A (en) * | 1998-12-08 | 2011-05-12 | Bayer Ag | Polycarbonate molding composition having improved mechanical property |
| JP2016204480A (en) * | 2015-04-20 | 2016-12-08 | 帝人株式会社 | Polycarbonate resin composition |
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