JPS6155809A - Conductive adhesive film wind - Google Patents
Conductive adhesive film windInfo
- Publication number
- JPS6155809A JPS6155809A JP17768484A JP17768484A JPS6155809A JP S6155809 A JPS6155809 A JP S6155809A JP 17768484 A JP17768484 A JP 17768484A JP 17768484 A JP17768484 A JP 17768484A JP S6155809 A JPS6155809 A JP S6155809A
- Authority
- JP
- Japan
- Prior art keywords
- base material
- adhesive layer
- connection
- adhesive
- adhesive film
- 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
- 239000002313 adhesive film Substances 0.000 title claims description 11
- 239000000463 material Substances 0.000 claims description 33
- 239000002245 particle Substances 0.000 claims description 23
- 239000012790 adhesive layer Substances 0.000 claims description 22
- 239000002923 metal particle Substances 0.000 claims description 12
- 238000004804 winding Methods 0.000 claims description 8
- 229920003023 plastic Polymers 0.000 claims description 4
- 239000004033 plastic Substances 0.000 claims description 4
- 238000002834 transmittance Methods 0.000 claims description 3
- 239000002985 plastic film Substances 0.000 claims description 2
- 229920006255 plastic film Polymers 0.000 claims description 2
- 239000000758 substrate Substances 0.000 claims 1
- 238000004381 surface treatment Methods 0.000 claims 1
- 230000001070 adhesive effect Effects 0.000 description 20
- 239000000853 adhesive Substances 0.000 description 19
- -1 polyethylene, ethylene-propylene Polymers 0.000 description 13
- 206010040844 Skin exfoliation Diseases 0.000 description 10
- 238000000034 method Methods 0.000 description 8
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 239000004743 Polypropylene Substances 0.000 description 6
- 229920001155 polypropylene Polymers 0.000 description 6
- 238000001035 drying Methods 0.000 description 5
- 238000009413 insulation Methods 0.000 description 5
- 239000010410 layer Substances 0.000 description 5
- 238000005520 cutting process Methods 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 239000004973 liquid crystal related substance Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 229910052759 nickel Inorganic materials 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
- 239000005977 Ethylene Substances 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 239000005038 ethylene vinyl acetate Substances 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 230000017525 heat dissipation Effects 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000011259 mixed solution Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920000139 polyethylene terephthalate Polymers 0.000 description 2
- 239000005020 polyethylene terephthalate Substances 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 238000003908 quality control method Methods 0.000 description 2
- 239000005060 rubber Substances 0.000 description 2
- 229920003048 styrene butadiene rubber Polymers 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 229920003002 synthetic resin Polymers 0.000 description 2
- 239000000057 synthetic resin Substances 0.000 description 2
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 description 1
- 229920002284 Cellulose triacetate Polymers 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 239000004971 Cross linker Substances 0.000 description 1
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004962 Polyamide-imide Substances 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 229920002367 Polyisobutene Polymers 0.000 description 1
- NNLVGZFZQQXQNW-ADJNRHBOSA-N [(2r,3r,4s,5r,6s)-4,5-diacetyloxy-3-[(2s,3r,4s,5r,6r)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6s)-4,5,6-triacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxyoxan-2-yl]methyl acetate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](OC(C)=O)[C@H]1OC(C)=O)O[C@H]1[C@@H]([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1)OC(C)=O)COC(=O)C)[C@@H]1[C@@H](COC(C)=O)O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O NNLVGZFZQQXQNW-ADJNRHBOSA-N 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000002390 adhesive tape Substances 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 230000003712 anti-aging effect Effects 0.000 description 1
- 229910052787 antimony Inorganic materials 0.000 description 1
- 238000000149 argon plasma sintering Methods 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000013040 bath agent Substances 0.000 description 1
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
- DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical class C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 239000011889 copper foil Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005401 electroluminescence Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 229920001038 ethylene copolymer Polymers 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- NJPPVKZQTLUDBO-UHFFFAOYSA-N novaluron Chemical compound C1=C(Cl)C(OC(F)(F)C(OC(F)(F)F)F)=CC=C1NC(=O)NC(=O)C1=C(F)C=CC=C1F NJPPVKZQTLUDBO-UHFFFAOYSA-N 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229920001084 poly(chloroprene) Polymers 0.000 description 1
- 229920003217 poly(methylsilsesquioxane) Polymers 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920002312 polyamide-imide Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 239000005056 polyisocyanate Substances 0.000 description 1
- 229920001228 polyisocyanate Polymers 0.000 description 1
- 239000001818 polyoxyethylene sorbitan monostearate Substances 0.000 description 1
- 235000010989 polyoxyethylene sorbitan monostearate Nutrition 0.000 description 1
- 229920000346 polystyrene-polyisoprene block-polystyrene Polymers 0.000 description 1
- 229920001289 polyvinyl ether Polymers 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 229920002379 silicone rubber Polymers 0.000 description 1
- 239000004945 silicone rubber Substances 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 230000035882 stress Effects 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 239000012745 toughening agent Substances 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
Landscapes
- Conductive Materials (AREA)
- Non-Insulated Conductors (AREA)
- Laminated Bodies (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】 〔産業上の利用分野〕 本発明は異方導電性接着フィルムの巻重体に関する。[Detailed description of the invention] [Industrial application field] The present invention relates to a roll of anisotropically conductive adhesive film.
液晶、EL(エレクトロルミネッセンス)、半導体集積
回路などの電子部品の小型、薄形、高精細化に伴い、こ
れら電子部品間あるいは、電子部品と回路系とを接続す
る高密度回路用の接続材料が要望されており、この目的
の為に異方導電性を有する成形品類が注目されている。As electronic components such as liquid crystals, EL (electroluminescence), and semiconductor integrated circuits become smaller, thinner, and more precise, connecting materials for high-density circuits that connect these electronic components or between electronic components and circuit systems are becoming more and more important. There is a strong demand for this, and molded products having anisotropic conductivity are attracting attention for this purpose.
異方導電性とは、一般的にはXYzの3方回軸のうち少
くとも一方向が導電性でかつ一方向が絶縁性であるもの
を云い、たとえば導電層とシリコンゴム等の絶縁層を交
互に構成したいわゆるゼブラ型異方導電ゴムや、絶縁層
の厚み方向に金属繊維を貫通させ二局部的に4電性を得
るもの等が知られているが、これらは接着性能を持たな
い為に別途固定手段を必要とし、また成形品を薄く機械
的に切出すために大きな形状の物は入手しに(い欠点を
有していた。Anisotropic conductivity generally refers to at least one direction being conductive and one direction being insulating among the three rotational axes of XYz, for example, a conductive layer and an insulating layer such as silicone rubber. There are known so-called zebra-type anisotropic conductive rubbers that have an alternating structure, and those that penetrate metal fibers in the thickness direction of an insulating layer to obtain quadrielectricity locally, but these do not have adhesive properties. In addition, since the molded product is mechanically cut into thin pieces, it is difficult to obtain large-sized products.
一方異方導電性の接着剤をシート状とする試みもありた
とえば次のような特徴を有している。On the other hand, there have been attempts to form anisotropically conductive adhesives into sheet shapes, which have the following characteristics, for example.
(1)加熱、加圧、6るいは加熱加圧という簡単な手段
により多数の回路量接続を同時に一度の接続操作により
完了できる。(1) Connection of a large number of circuits can be completed simultaneously with a single connection operation by simple means of heating, pressurizing, or heating and pressurizing.
(2) シート状である為に、厚みが均一で導電性の
バラツキが少(接続信頼性が高い。(2) Because it is in sheet form, the thickness is uniform and there is little variation in conductivity (high connection reliability).
(5)無溶剤である為に、接続作業時に一般の接着剤類
にみられるような溶剤等による環境汚染がない。(5) Since it is solvent-free, there is no environmental pollution caused by solvents, etc., which is seen with general adhesives during connection work.
しかしながらか〜る接着シートは厚みが比較的厚くまた
接着剤成分が硬質なため巻物状となし難いため予め所定
形状に打抜いた小片状として供給されており、回路接続
の自動化が難かしい状況にあった。However, since such adhesive sheets are relatively thick and the adhesive component is hard, it is difficult to form them into rolls, so they are supplied in the form of small pieces punched into predetermined shapes, making it difficult to automate circuit connections. It was there.
〔発明が解決しようとする問題点〕
本発明はか〜る状況に鑑みなされたもので回路接続の自
動化を可能にするとともに接続信頼性にすぐれた異方導
電性接着フィルムの巻重体を提供せんとするものである
。[Problems to be Solved by the Invention] The present invention has been made in view of the above circumstances, and provides a rolled body of anisotropically conductive adhesive film that enables automation of circuit connections and has excellent connection reliability. That is.
すなわち本発明は剥離性基材上に、平均粒径が001〜
50μm″′Cめる金属靭子をα1〜10体積%不均一
分散させてなる、厚さが100μm以下の可撓性接着剤
層を形成してなる長尺テープを巻芯上に多重巻回してな
る異方4を性接着フィルム巻重体に関する。That is, in the present invention, on a removable base material, an average particle size of 001 to
A long tape formed by forming a flexible adhesive layer with a thickness of 100 μm or less, which is made by non-uniformly dispersing 50 μm″′C metal toughener by α1 to 10% by volume, is wound multiple times on a winding core. The present invention relates to an anisotropic 4 adhesive film roll.
以下本発明を実施例を示した図面を参照しながら説明す
ると第1図は本発明に係る異方感電性接着フィルム1の
断面を示したもので基本的には剥離性基材4と導電性金
属粒子3を不均一分散させてなる接着剤層2とからなっ
ている。The present invention will be described below with reference to drawings showing examples. FIG. 1 shows a cross section of an anisotropic electrosensitive adhesive film 1 according to the present invention, which basically consists of a removable base material 4 and a conductive film. It consists of an adhesive layer 2 formed by non-uniformly dispersing metal particles 3.
本発明で用いられる接着剤成分としては可撓性と絶縁性
を有するものであれば特に限定されないが例えばエチレ
ン酢酸ビニル共重合体、エチレン−酢酸ビニル共重合体
変性物、ポリエチレン、エチレン−プロピレンulF体
、エチレン・アクリル酸共重合体、エチレン−アクリル
酸エステル共重合体、エチレン−アクリル酸塩共重合体
、アクリル酸エステル系ゴム、ポリイソブチレン、アタ
クチックポリプロピレン、ポリビニルブチラール、アク
リロニトリル−ブタジェン共重合体、スチレン−ブタジ
ェンブロック共重合体、スチレン−イソプレンブロック
共重合体、ポリブタジェン、エチレンセルロース、ポリ
エステル、ポリアミド、ボリクレタン、天然ゴム、シリ
エン系ゴム、ポリクロロプレン、ポリビニルエーテルな
どが適用可能であり単独あるいは2種以上が併用して用
いられる。The adhesive component used in the present invention is not particularly limited as long as it has flexibility and insulation, but examples include ethylene-vinyl acetate copolymer, modified ethylene-vinyl acetate copolymer, polyethylene, ethylene-propylene ULF. polyisobutylene, atactic polypropylene, polyvinyl butyral, acrylonitrile-butadiene copolymer , styrene-butadiene block copolymer, styrene-isoprene block copolymer, polybutadiene, ethylene cellulose, polyester, polyamide, polycrethane, natural rubber, silyene rubber, polychloroprene, polyvinyl ether, etc. can be used alone or in combination. More than one species is used in combination.
接着剤成分としては上記各種ポリマの他必俄に応じアル
キルフェノール等の粘着付与剤、ジオクチルフタレート
等の可塑剤、ポリイソシアネート等の架橋剤の他充填剤
、分散剤、老化防止剤などの1種あるいは2種以上が併
用される。In addition to the above-mentioned various polymers, adhesive components may also include tackifiers such as alkylphenols, plasticizers such as dioctyl phthalate, crosslinkers such as polyisocyanate, fillers, dispersants, anti-aging agents, etc. Two or more types are used in combination.
導電性を付与するために用いられる金属粒子としては平
均粒径が0.01〜50μmのものが用いられる。粒径
0.01μm以下では、粒子の表面積が大きく粒子間の
接触が必賛以上に生じることから面方向の絶縁性が得ら
れない。The metal particles used to impart conductivity have an average particle size of 0.01 to 50 μm. If the particle size is 0.01 μm or less, the surface area of the particles is large and contact between the particles occurs more than necessary, making it impossible to obtain insulating properties in the plane direction.
また平均粒径50μm以上では、回路が微細の場合に隣
接回路間に粒子が存在する確率が高くなり、やはり面方
向の絶縁性が得られない。Further, if the average particle diameter is 50 μm or more, the probability that particles will exist between adjacent circuits increases when the circuits are fine, and insulation in the plane direction cannot be obtained.
ここで平均粒佳日は次式で求めるものとする。Here, the average grain good day is calculated using the following formula.
D:J:nd/Σn
nはdなる粒径の粒子の数を示す。これら粒径の観察方
法としては、一般的に用いられる電子顕微鏡や光学顕微
鏡、コールタカウンター、光散乱法などがある。D:J:nd/Σn n indicates the number of particles having a particle size of d. Methods for observing these particle sizes include commonly used electron microscopes, optical microscopes, Coulter counters, light scattering methods, and the like.
導電性粒子として金属粒子を用いるのは接続回路部の熱
放散性の良いことによる。接続部における熱放散性が悪
いと、接続部が回路を流れる電流によりジュール熱で発
熱し、極端な場合には接続部が剥離する。The reason why metal particles are used as the conductive particles is that they have good heat dissipation properties in the connecting circuit portion. If heat dissipation in the connection is poor, the connection will generate heat due to Joule heat due to the current flowing through the circuit, and in extreme cases, the connection will separate.
これら金属粒子の例としては、Fe、 Ni、 Cr。Examples of these metal particles include Fe, Ni, and Cr.
Co、 All、 Sb、 Mo、 Cu、 Ag、
Pt、 Au 等があり、これらの単体あるいは合金や
酸化物などでもよく、これらの2種以上を待合して用い
ることも可能である。また金属粒子の中には、ガラスや
合成樹脂の表面に前記金属層を設けた物でも適用可能で
ある。Co, All, Sb, Mo, Cu, Ag,
There are Pt, Au, etc., and these materials may be used alone, as an alloy, or as an oxide, and it is also possible to use two or more of these materials in combination. Furthermore, among the metal particles, those having the metal layer provided on the surface of glass or synthetic resin can also be used.
これら導電性金属粒子の含有量は0.1〜10体積%が
良好な異方41!性を示す。The content of these conductive metal particles is preferably 0.1 to 10% by volume 41! Show your gender.
0.1体積%以下では、微細回路の接続において厚み方
向の4電性が得られにくく、10体積%以上では隣接回
路間の絶縁性が得られなくなる。If it is less than 0.1 volume %, it is difficult to obtain tetraelectricity in the thickness direction in connection of fine circuits, and if it is more than 10 volume %, insulation between adjacent circuits cannot be obtained.
このような理由から信頼性の隅い異方導篭性を得る為の
含有量は0.5〜5体稍%がさらに好ましい。For these reasons, the content is more preferably 0.5 to 5% in order to obtain reliable anisotropic conductivity.
粒子形状ははy球状であることが回路接続時における粒
子相互あるいは粒子と回路面との接触を得やすいことか
ら好ましい。It is preferable that the particles have a spherical shape because this facilitates contact between the particles or between the particles and the circuit surface during circuit connection.
これら導電性金属粒子は、絶縁性接着剤の中に不均一分
散している。すなわち厚み方向に密集して回路接続後に
導電性を付与し、一方面方向にはランダム状に分散して
いるために回路接続時において面方向にはいかなる方向
にも導電性を有しない。 ゛
接着剤層の厚みは100μm以下が透明性、可撓性を得
るために好ましい。かよる接着剤層はJIS K−6
714による全光線透過率が40%以上を保持している
。These conductive metal particles are non-uniformly dispersed within the insulating adhesive. That is, they are densely packed in the thickness direction and provide conductivity after circuit connection, and are randomly distributed in one surface direction, so that they do not have conductivity in any direction in the surface direction when circuit connection is made. ``The thickness of the adhesive layer is preferably 100 μm or less in order to obtain transparency and flexibility. The adhesive layer is JIS K-6
714, the total light transmittance is maintained at 40% or more.
接着剤層が透明性を有すると、製造時の品質管理が行な
い易くまた回路接続時における位置合せを接着剤層を透
視して行なえるので、非常に作業性が良好である。When the adhesive layer is transparent, quality control during manufacturing is easy to perform, and alignment during circuit connection can be performed by looking through the adhesive layer, resulting in very good workability.
またか〜る接着剤層は薄くフレキシビリティに富んでお
り巻重体とすることが容易であり、さらに接続作業時回
路接続部に応力が加わった場合にも追随性が高(、まだ
回路接続部を折曲げる等も可能となり機器を設計する際
に自由度が大きい。In addition, the adhesive layer is thin and highly flexible, making it easy to roll up into rolls. Furthermore, it has high followability even when stress is applied to the circuit connection during connection work (although the circuit connection still remains It is also possible to bend the material, giving a greater degree of freedom when designing equipment.
剥離性基材としては接着剤層との剥店力が2〜200g
/191!1In(JIS C−2107準拠)の範
囲になるものから選択される。As a removable base material, the peeling force with the adhesive layer is 2 to 200 g.
/191!1In (based on JIS C-2107).
剥離力が2g/19IIII11以下であると接続操作
時に剥離し易(、また、200g/19mm以上である
と、剥離し難くなり接続作業性が劣る。If the peeling force is less than 2 g/19III11, it will be easy to peel off during the connection operation (and if it is more than 200 g/19 mm, it will be difficult to peel off and the connection workability will be poor).
上記適度な剥離力を得るためには基材の濡れ指数(JI
S K−6768)を目安とすることが可能であり、
接着剤の濡れ指数より略5dyれ/ cm以上小さいこ
とが選定の目安となる。In order to obtain the above-mentioned appropriate peeling force, it is necessary to
SK-6768) can be used as a guide,
The standard for selection is approximately 5 dy/cm or more smaller than the wetting index of the adhesive.
か〜る剥離力を得るためには基材表面にシリコーンやポ
リビニルカルバメート等の剥離処理をしたものでもよい
がこの場合にはできるだけ接着剤層への転着、移行性の
ないものでないと接着力あるいは信頼性の低下を招(。In order to obtain such a peeling force, the surface of the base material may be treated with a release agent such as silicone or polyvinyl carbamate, but in this case, it is necessary to use a material that does not transfer or migrate to the adhesive layer as much as possible. Or it may lead to a decrease in reliability (.
また繊維性基材は異物が接着剤層につき易いため好まし
くない。Furthermore, a fibrous base material is not preferred because foreign matter tends to adhere to the adhesive layer.
上記条件を満すものとしては接着剤との組合せによって
も異なるがポリエチレン、ポリプロピレン、ポリエチレ
ンテレフタレート、セルローズトリアセテート、6フツ
化ポリプロピレン、42)化エチレン、4フッ化エチレ
ン−エチレン共重合体、ポリ2ツ化ビニリデン、ポリア
ミド、ポリイミドなどの各種プラスチックフィルムを用
いることができる。Things that meet the above conditions vary depending on the combination with the adhesive, but polyethylene, polypropylene, polyethylene terephthalate, cellulose triacetate, hexafluorinated polypropylene, 42) ethylene, tetrafluorinated ethylene-ethylene copolymer, polyethylene Various plastic films such as vinylidene chloride, polyamide, and polyimide can be used.
また剥離性基材は透明性を有するもの、あるいは不透明
性であるものどちらも適用可能である。透明性である場
合には、接着層のもつ透明性と合わせて製品に美観を与
え、また製造時における品質管理が行ない易い。Furthermore, the releasable base material may be either transparent or opaque. When the adhesive layer is transparent, it gives the product an aesthetic appearance together with the transparency of the adhesive layer, and quality control during manufacturing is easier.
一方剥離性基材が不透明性である場合においては、仮接
続後の剥離性基材の剥し忘れを防止することが可能とな
る。剥離性基材は接着剤層を挾んでサンドイッチ状に配
置してもよいう以上の構成材料を用いた巻重体の製造方
法は接着剤成分としてのポリマーおよびその他の必要に
応じて使用する添加剤からなる接着剤組成物を溶剤に溶
解し液状とした後に、導電性金属粒子を通常の攪拌等に
より混合し、セパレータ等の基材上に塗布し、乾燥時の
浴剤揮散による厚み方向の体積収縮により金属粒子を厚
み方向に配列“、密集化する方法、るるいは導′成性接
着剤組成物を磁場下で成形して、磁性を有する導電性金
属粒子を厚み方向に配列するなどの方法により導電性粒
子が異方配列した接着剤を得ることが可能でありこの物
をロール状に巻取ることにより巻重体が得られる。基本
的にはフィルムの厚み方向に粒子が苦集構造をとり面方
向にはランダム状に分布すれば良いので、製造方法は特
に問わない。On the other hand, when the releasable base material is opaque, it is possible to prevent forgetting to peel off the releasable base material after temporary connection. The releasable base material may sandwich the adhesive layer and be arranged in the form of a sandwich.The method for producing a rolled body using the above constituent materials includes a polymer as an adhesive component and other additives used as necessary. After dissolving the adhesive composition in a solvent to make it liquid, conductive metal particles are mixed by normal stirring, etc., and applied onto a base material such as a separator, and the volume in the thickness direction is reduced by volatilization of the bath agent during drying. Methods include arranging and densifying metal particles in the thickness direction by shrinkage, molding a lubricant or conductive adhesive composition under a magnetic field, and arranging magnetic conductive metal particles in the thickness direction. By this method, it is possible to obtain an adhesive in which conductive particles are arranged anisotropically, and by winding this material into a roll, a rolled body can be obtained.Basically, the particles form an arrangement structure in the thickness direction of the film. The manufacturing method is not particularly limited as long as it is distributed randomly in the direction of the cutting surface.
接着剤層の厚みは100μm以下であることが必要であ
る。The thickness of the adhesive layer needs to be 100 μm or less.
すなわち厚みが100μm以上では、電気抵抗のレベル
が増大しまた、回路接続の信頼性が低下し易(、また可
撓性、透明度が悪(なるため好ましくない。That is, if the thickness is 100 μm or more, the electrical resistance level increases, the reliability of circuit connection tends to decrease (and the flexibility and transparency deteriorate), which is not preferable.
第2図は巻重体を示す模式図であるが巻芯5はプラスチ
ック↓のものが細巾テープに切断する際接着剤層に異物
がつかないため好ましい。FIG. 2 is a schematic diagram showing the roll body, and it is preferable that the core 5 is made of plastic because foreign matter does not stick to the adhesive layer when cutting into a narrow tape.
連続状に巻取られた巻重体は通常2m以下の製品中を有
するが、この広巾巻重体の場合においてはたとえば多層
回路配線板のスルホール代替FA;bるいはハイブリッ
ドICの基板回路への接続材として連続状で供給できる
ことから有用である。Continuously wound rolls usually have a product length of 2 m or less, but in the case of this wide roll, they can be used, for example, as a through-hole substitute for multilayer circuit wiring boards; It is useful because it can be supplied continuously.
一方広巾巻重体を、通常の手段すなわちスリット刃によ
り巻取時に細巾に切断するあるいは広巾巻重体を回転刃
を用いてブツ切りするなどの方法により細巾のテープ状
となすことも可能である(第3図)。On the other hand, it is also possible to make a wide rolled material into a narrow tape shape by a conventional method, such as cutting the wide rolled material into narrow strips during winding with a slit blade, or cutting the wide rolled material into pieces using a rotary blade. (Figure 3).
細巾テープ状であると、たとえば液晶標示素子と回路系
との接続の場合のように、接続面積がきわめて細い場合
等において、接続材料としてのテープを一定巾で連続供
給できることから接続工程の自動化が可能となる長所を
有する。If it is in the form of a narrow tape, it can automate the connection process because it can continuously supply a constant width of tape as a connection material when the connection area is extremely narrow, such as when connecting a liquid crystal display element to a circuit system. It has the advantage of being possible.
テープ状とした場合の巾は任意にできるが通常1〜10
順ものとして供給される。When made into a tape, the width can be set arbitrarily, but it is usually 1 to 10.
Supplied as ordered.
本発明になる巻重体の用途としては、液晶、EL、太陽
電池等の表示素子類と回路系との接続、IC等の電子部
品の!4@と回路基板系との接続、その他メンブレンス
イッチ、多層印刷配線板への適用等がある。The rolled body of the present invention can be used for connecting display elements such as liquid crystals, EL, solar cells, and circuit systems, and for electronic components such as ICs! Applications include connections between 4@ and circuit board systems, membrane switches, and multilayer printed wiring boards.
以下本発明を実施例によりさらに詳細に説明する。The present invention will be explained in more detail below using examples.
導電性金属粒子は乾燥後の絶縁性接着剤に対する体積%
で表示した。また得られた巻重体の特性評価は、ライン
巾α1關、ピッチQ、2mm0銅箔と合成樹脂層の交互
に連続する7レキシプル回路板(以下FPCと略す)同
士を接続中5mroで接続して評価した。Conductive metal particles are % by volume of insulating adhesive after drying
It was displayed in In addition, the characteristics of the obtained rolled body were evaluated by connecting 7 lexiple circuit boards (hereinafter abbreviated as FPC) with line width α1, pitch Q, 2 mm0, which are made of copper foil and synthetic resin layers at 5 mRO during connection. evaluated.
実施例−1
分子量約20.000の熱可塑性ポリエステルをメチル
エチルケトンに溶解し、固形分55%の溶液を得た(A
液)n
一方粒径0.03μmのニッケル粒子を界面活性剤を含
むメタノール中に濃度50%となるように超音波分散し
た。ここに界面活性剤はノニオン系のポリオキシエチレ
ンソルビタンモノステアレートをメタノール中に10%
含有させた。Example-1 A thermoplastic polyester with a molecular weight of about 20.000 was dissolved in methyl ethyl ketone to obtain a solution with a solid content of 55% (A
Liquid) n On the other hand, nickel particles with a particle size of 0.03 μm were ultrasonically dispersed in methanol containing a surfactant to a concentration of 50%. Here, the surfactant is 10% nonionic polyoxyethylene sorbitan monostearate in methanol.
Contained.
以上により粒径a03μmのニッケル粉は侠集すること
なく単独粒子として存在できるようになった(Bぼ)、
。As a result of the above, nickel powder with a particle size of 03 μm can now exist as a single particle without agglomeration (B).
.
A液とB液をニッケル分がcL5体積%となるように配
合してボールミルで5時間混合分散した。この配合液を
、ロールコータにより延伸ポリプロピレンフィルム(m
れ指数30 dyn / cco)50μm上に、乾燥
後の厚みが10μmとなるように塗布し、100℃−5
分乾燥して溶媒を除去した後にプラスチック芒に巻取り
巻重体を得た。この巻重体は有効&品巾1mであり巻長
さけ任意てらったが100m巻とした。Solutions A and B were blended so that the nickel content was 5% by volume cL, and mixed and dispersed in a ball mill for 5 hours. This mixed solution is applied to a stretched polypropylene film (m
It was coated on a surface of 50 μm (with a friction index of 30 dyn/cco) so that the thickness after drying was 10 μm, and it was heated at 100°C-5
After drying for several minutes to remove the solvent, the product was wound around a plastic awn to obtain a roll. This roll body had an effective width of 1 m, and the winding length was arbitrarily set, but it was wound as 100 m.
この巻重体をスリット巾5mm″’lfl巾に巻替えス
リットを行ない多数のテープ状巻重体を得た。This rolled body was re-wound and slit to a slit width of 5 mm'' lfl width to obtain a large number of tape-shaped rolled bodies.
このテープ状巻重体を用いて、一方のFPCの片面に載
置して100℃−5kg/an’−5秒の加熱加圧によ
り仮接続を行なったあとポリプロピへ
レンフィルラを剥離して、さらに他のFPCを前記剥離
面にのせて回路が一致するように位置合せ後に、さらに
150℃−5kg/−−1o秒間の加熱加圧によりFP
C同士を対向させて接続した。Using this tape-shaped roll, place it on one side of one FPC, heat and pressurize at 100°C-5kg/an'-5 seconds to make a temporary connection, then peel off the polypropylene filler, and then After placing the FPC on the peeled surface and aligning it so that the circuits match, the FP is further heated and pressurized at 150°C for 5 kg/--10 seconds.
The Cs were connected facing each other.
この物の特性を第1表に示すが、仮貼付後に基材は接着
面より簡単に剥離可能であり、接続したFPCを60℃
−90%RH槽中にて1,000Hr処理後も大きな劣
化は見られなかった。The properties of this product are shown in Table 1. After temporary attachment, the base material can be easily peeled off from the adhesive surface, and the connected FPC can be heated at 60°C.
No major deterioration was observed even after treatment for 1,000 hours in a −90% RH tank.
★だ隣接する回路間の抵抗は101OΩ以上であり、処
理前後ともに充分な絶縁性を示した。★ The resistance between adjacent circuits was 101 OΩ or more, indicating sufficient insulation both before and after treatment.
実施例−2
スチレン−ブタジェンのブロック共重合体100重量部
と軟化点100℃の芳香族系粘着付与剤50重量部およ
びトルエン200重量剖よりなる絶縁性接着剤溶液を作
成し、この溶液に平均粒径20μmのニッケル粉を乾燥
後の接着剤に対して10体積%となるように混合した。Example 2 An insulating adhesive solution was prepared consisting of 100 parts by weight of a styrene-butadiene block copolymer, 50 parts by weight of an aromatic tackifier with a softening point of 100°C, and 200 parts by weight of toluene. Nickel powder having a particle size of 20 μm was mixed in an amount of 10% by volume with respect to the dried adhesive.
この混合液を6フツ化ポリプロピレンシート<siすれ
指数35 dyn/C+n ) 100 ttm上に乾
燥後の厚みが50μmとなるように実施例−1と同様に
塗布して有効製品中5QQaun長さ100mの巻重体
を得た。This mixed solution was applied onto a hexafluoride polypropylene sheet <si abrasion index 35 dyn/C+n) 100 ttm in the same manner as in Example 1 so that the thickness after drying would be 50 μm. A rolled body was obtained.
この巻重体を用いて仮接続温度を150℃とした他は全
て実施例−1と同様に接続評価した。Connection was evaluated in the same manner as in Example-1 except that this rolled body was used and the temporary connection temperature was 150°C.
この場合剥離性基材の耐熱性が高(150℃の仮貼付が
可能であった。また隣接回路間はlQ100以上と十分
な絶縁性を示した。In this case, the releasable base material had high heat resistance (temporary attachment at 150° C. was possible), and sufficient insulation between adjacent circuits was demonstrated with lQ of 100 or more.
比較例
剥離性基材として比較例−1のシリコン処理ヲ行すった
ポリエチレンテレフタレートフィルムを用いた他は実施
例−2と全(同様にして巻重体を得、実施例−2と同様
な評価を行なった結果を@1表に示す。この場合実施例
−2に較べて接着力が低(接続部の抵抗も高かった。Comparative Example The same procedure as in Example 2 was used except that the silicone-treated polyethylene terephthalate film of Comparative Example 1 was used as the releasable base material. The results are shown in Table 1. In this case, the adhesive strength was lower than in Example-2 (the resistance at the connection portion was also high).
また比較例においては、接着剤層と剥離性基材の相方が
透明性であり、仮接続後に剥離性基材の剥し忘れをし易
かりたが、実施例−2においては剥離性基材が、白色状
であり剥し忘れのミスがなかった。In addition, in the comparative example, the adhesive layer and the releasable base material were transparent, making it easy to forget to remove the releasable base material after temporary connection, but in Example-2, the releasable base material was , it was white and there was no mistake of forgetting to remove it.
第 1 表
第1表において
(1)仮接続後の基材の剥離力はJISC−2107に
準拠して、90度剥離、速度300mm1分、測定は2
0℃で行なった。なお90度剥離とする為に仮貼付後の
FPCを両面粘着テープにより台座に固定して測定した
。Table 1 In Table 1, (1) Peeling force of the base material after temporary connection was determined based on JISC-2107, 90 degree peeling, speed 300mm 1 minute, measurement was 2
It was carried out at 0°C. In order to achieve 90 degree peeling, the FPC after temporary attachment was fixed to a pedestal with double-sided adhesive tape and measured.
(2)接着剤層の全光線透過率はJISK−6714に
準拠して日本電色工業製デジタル濁度計DH−20Dに
より測定した。(2) The total light transmittance of the adhesive layer was measured using a digital turbidimeter DH-20D manufactured by Nippon Denshoku Industries in accordance with JISK-6714.
(3)接着力)tJIs Z−0257VC準拠シテ
90度剥離法にて行ない、一方のFPCをアルミニウム
板1.011111f tで背面から補強した。(3) Adhesive strength) tJIs Z-0257VC compliant 90 degree peeling method was used, and one FPC was reinforced from the back side with an aluminum plate of 1.011111ft.
剥離速度は50fflIII/分測定は20℃−65%
RHで行なった。Peeling speed is 50fflIII/min Measured at 20℃-65%
This was done at RH.
(4)抵抗は接続部を含むFPCの対向する″rJL極
間の抵抗をマルチメータて測定した。(4) The resistance was measured using a multimeter between the opposing "rJL" poles of the FPC including the connection part.
(5)初期値は、接続後1日以内に測定した。また老化
波特性は接続したFPCを60℃−90%RHの恒温恒
湿下で1,000Hr処坤後の測定値である。(5) Initial values were measured within one day after connection. The aging wave characteristics are measured values after the connected FPC was subjected to constant temperature and humidity at 60° C. and 90% RH for 1,000 hours.
4、発明の効果
以上詳述したように本発明になる異方導′屯性接着フィ
ルム巻重体は連続ロール状であるとともに巻戻し性、透
明性にすぐれるため接続工程を自動化することが可能と
なつた。4. Effects of the Invention As detailed above, the anisotropically conductive adhesive film roll of the present invention is in the form of a continuous roll and has excellent unwinding properties and transparency, making it possible to automate the connection process. It became.
また剥離処理していない剥離性基材および巻芯なプラス
チック製とすnば、接着剤層への異物の混入、付着がさ
けられ接続信頼性の向上をはかることができる。Furthermore, by using a peelable base material that has not been subjected to peeling treatment and a core made of plastic, it is possible to prevent foreign matter from entering or adhering to the adhesive layer, thereby improving connection reliability.
図面はいずれも本発明の実施例を示すもので第1図は接
着フィルムの断明図、第2図および第3図は巻重体の斜
視図である。
符号の説明
1、 接着フィルム 2.#着剤層五 s′eL性
粒子 4.剥除性基材5、巻芯The drawings all show embodiments of the present invention; FIG. 1 is a cutaway view of the adhesive film, and FIGS. 2 and 3 are perspective views of the rolled body. Explanation of symbols 1. Adhesive film 2. #Adhesive layer 5 s'eL particles 4. Peelable base material 5, winding core
Claims (1)
ある金属粒子を0.1〜10体積%不均一分散させてな
る、厚さが100μm以下の可撓性接着剤層を形成して
なる長尺テープを巻芯上に多重巻回してなる異方導電性
接着フィルム巻重体。 2、剥離性基材と接着剤層との剥離強度(JIS C−
2107)が2g/19mm〜200g/19mmであ
る特許請求の範囲第1項記載の異方導電性接着フィルム
巻重体。 3、剥離性基材が表面処理がされていないプラスチック
フィルムであり巻芯がプラスチック製巻芯である特許請
求の範囲第1項または第2項記載の導電性接着フィルム
巻重体。 4、接着剤層が全光線透過率(JIS K−6714)
40%以上を有するとともに貫層方向にのみ導電性を有
するものである特許請求の範囲第1項乃至第3項いずれ
かに記載の異方導電性接着フィルム巻重体。[Claims] 1. A removable substrate with a thickness of 100 μm or less, which is made by dispersing 0.1 to 10% by volume of metal particles with an average particle size of 0.01 to 50 μm on a removable base material. An anisotropically conductive adhesive film roll made by multiple windings of a long tape formed with a flexible adhesive layer on a core. 2. Peel strength between peelable base material and adhesive layer (JIS C-
2107) is 2 g/19 mm to 200 g/19 mm, the anisotropically conductive adhesive film roll according to claim 1. 3. The conductive adhesive film roll according to claim 1 or 2, wherein the releasable base material is a plastic film without surface treatment and the winding core is a plastic winding core. 4. Adhesive layer has total light transmittance (JIS K-6714)
40% or more and has conductivity only in the translayer direction.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP17768484A JPS6155809A (en) | 1984-08-27 | 1984-08-27 | Conductive adhesive film wind |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP17768484A JPS6155809A (en) | 1984-08-27 | 1984-08-27 | Conductive adhesive film wind |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS6155809A true JPS6155809A (en) | 1986-03-20 |
Family
ID=16035295
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP17768484A Pending JPS6155809A (en) | 1984-08-27 | 1984-08-27 | Conductive adhesive film wind |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6155809A (en) |
Cited By (8)
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JPS6333513U (en) * | 1986-08-20 | 1988-03-04 | ||
JPH01232735A (en) * | 1988-03-11 | 1989-09-18 | Matsushita Electric Ind Co Ltd | Semiconductor device |
JPH04169080A (en) * | 1990-10-31 | 1992-06-17 | Shin Etsu Polymer Co Ltd | Hot setting type anisotropic conductive connection member |
JPH0487119U (en) * | 1990-12-05 | 1992-07-29 | ||
JPH0487118U (en) * | 1990-12-05 | 1992-07-29 | ||
US6190578B1 (en) | 1996-02-08 | 2001-02-20 | Asahi Kasei Kogyo Kabushiki Kaisha | Anisotropic conductive composition |
JP2006218135A (en) * | 2005-02-14 | 2006-08-24 | Masaharu Numakura | Mat |
JP2017518611A (en) * | 2014-05-21 | 2017-07-06 | コンダライン エーエス | Method for forming an article comprising a particle path with an exposed end |
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JPS51101040A (en) * | 1975-03-04 | 1976-09-07 | Suwa Seikosha Kk | |
JPS57182909A (en) * | 1981-05-06 | 1982-11-11 | Kanegafuchi Chemical Ind | Anisotropically conductive sheet |
JPS5823174A (en) * | 1981-07-31 | 1983-02-10 | 信越ポリマー株式会社 | Connector |
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- 1984-08-27 JP JP17768484A patent/JPS6155809A/en active Pending
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS51101040A (en) * | 1975-03-04 | 1976-09-07 | Suwa Seikosha Kk | |
JPS57182909A (en) * | 1981-05-06 | 1982-11-11 | Kanegafuchi Chemical Ind | Anisotropically conductive sheet |
JPS5823174A (en) * | 1981-07-31 | 1983-02-10 | 信越ポリマー株式会社 | Connector |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6333513U (en) * | 1986-08-20 | 1988-03-04 | ||
JPH01232735A (en) * | 1988-03-11 | 1989-09-18 | Matsushita Electric Ind Co Ltd | Semiconductor device |
JPH04169080A (en) * | 1990-10-31 | 1992-06-17 | Shin Etsu Polymer Co Ltd | Hot setting type anisotropic conductive connection member |
JPH0487119U (en) * | 1990-12-05 | 1992-07-29 | ||
JPH0487118U (en) * | 1990-12-05 | 1992-07-29 | ||
US6190578B1 (en) | 1996-02-08 | 2001-02-20 | Asahi Kasei Kogyo Kabushiki Kaisha | Anisotropic conductive composition |
JP2006218135A (en) * | 2005-02-14 | 2006-08-24 | Masaharu Numakura | Mat |
JP2017518611A (en) * | 2014-05-21 | 2017-07-06 | コンダライン エーエス | Method for forming an article comprising a particle path with an exposed end |
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