JPS62165886A - Jointing member of circuiy - Google Patents
Jointing member of circuiyInfo
- Publication number
- JPS62165886A JPS62165886A JP833286A JP833286A JPS62165886A JP S62165886 A JPS62165886 A JP S62165886A JP 833286 A JP833286 A JP 833286A JP 833286 A JP833286 A JP 833286A JP S62165886 A JPS62165886 A JP S62165886A
- Authority
- JP
- Japan
- Prior art keywords
- particles
- connecting member
- circuit
- conductive
- circuits
- 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
- 239000002245 particle Substances 0.000 claims description 76
- 230000001070 adhesive effect Effects 0.000 claims description 25
- 239000000853 adhesive Substances 0.000 claims description 24
- 239000011162 core material Substances 0.000 claims description 23
- 239000002184 metal Substances 0.000 claims description 17
- 229910052751 metal Inorganic materials 0.000 claims description 17
- 229920001187 thermosetting polymer Polymers 0.000 claims description 16
- 229920005989 resin Polymers 0.000 claims description 9
- 239000011347 resin Substances 0.000 claims description 9
- 238000002834 transmittance Methods 0.000 claims description 3
- 239000010410 layer Substances 0.000 description 13
- 238000000034 method Methods 0.000 description 12
- 238000009413 insulation Methods 0.000 description 8
- 239000002904 solvent Substances 0.000 description 8
- 239000010931 gold Substances 0.000 description 7
- 238000010438 heat treatment Methods 0.000 description 7
- 239000000203 mixture Substances 0.000 description 7
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 6
- 229910052737 gold Inorganic materials 0.000 description 6
- 229920000642 polymer Polymers 0.000 description 6
- 238000011156 evaluation Methods 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 239000004020 conductor Substances 0.000 description 4
- -1 polyethylene, ethylene-propylene copolymer Polymers 0.000 description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000013040 bath agent Substances 0.000 description 3
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- 230000007423 decrease Effects 0.000 description 3
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- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 2
- 239000004593 Epoxy Substances 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- 229920000877 Melamine resin Polymers 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 2
- 206010040844 Skin exfoliation Diseases 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- QXJJQWWVWRCVQT-UHFFFAOYSA-K calcium;sodium;phosphate Chemical compound [Na+].[Ca+2].[O-]P([O-])([O-])=O QXJJQWWVWRCVQT-UHFFFAOYSA-K 0.000 description 2
- 239000004202 carbamide Substances 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
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- 238000009472 formulation Methods 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- 239000002923 metal particle Substances 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 229920000647 polyepoxide Polymers 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 229920001721 polyimide Polymers 0.000 description 2
- 229920001228 polyisocyanate Polymers 0.000 description 2
- 239000005056 polyisocyanate Substances 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 239000012798 spherical particle Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 229920003051 synthetic elastomer Polymers 0.000 description 2
- 239000005061 synthetic rubber Substances 0.000 description 2
- 150000003505 terpenes Chemical class 0.000 description 2
- 235000007586 terpenes Nutrition 0.000 description 2
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- HECLRDQVFMWTQS-RGOKHQFPSA-N 1755-01-7 Chemical compound C1[C@H]2[C@@H]3CC=C[C@@H]3[C@@H]1C=C2 HECLRDQVFMWTQS-RGOKHQFPSA-N 0.000 description 1
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 description 1
- DGXAGETVRDOQFP-UHFFFAOYSA-N 2,6-dihydroxybenzaldehyde Chemical compound OC1=CC=CC(O)=C1C=O DGXAGETVRDOQFP-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
- 239000004641 Diallyl-phthalate Substances 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- 229910052765 Lutetium Inorganic materials 0.000 description 1
- 229920000459 Nitrile rubber Polymers 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 229910052770 Uranium Inorganic materials 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 239000002280 amphoteric surfactant Substances 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 230000003712 anti-aging effect Effects 0.000 description 1
- 229910052787 antimony Inorganic materials 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 229910052785 arsenic Inorganic materials 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 238000000889 atomisation Methods 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 1
- 239000012964 benzotriazole Substances 0.000 description 1
- 229910052790 beryllium Inorganic materials 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
- QUDWYFHPNIMBFC-UHFFFAOYSA-N bis(prop-2-enyl) benzene-1,2-dicarboxylate Chemical compound C=CCOC(=O)C1=CC=CC=C1C(=O)OCC=C QUDWYFHPNIMBFC-UHFFFAOYSA-N 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- JPPGWVWBAJLHCE-UHFFFAOYSA-N buta-1,3-diene;ethene Chemical compound C=C.C=CC=C JPPGWVWBAJLHCE-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000002843 carboxylic acid group Chemical group 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 239000011231 conductive filler Substances 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 239000002612 dispersion medium Substances 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 229920006228 ethylene acrylate copolymer Polymers 0.000 description 1
- 229920006242 ethylene acrylic acid copolymer Polymers 0.000 description 1
- 229920006226 ethylene-acrylic acid Polymers 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 238000007757 hot melt coating Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- YAMHXTCMCPHKLN-UHFFFAOYSA-N imidazolidin-2-one Chemical compound O=C1NCCN1 YAMHXTCMCPHKLN-UHFFFAOYSA-N 0.000 description 1
- 229910052738 indium Inorganic materials 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
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- 239000003607 modifier Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- NNQIBXKOCAMOOS-UHFFFAOYSA-N phenyl hypofluorite Chemical compound FOC1=CC=CC=C1 NNQIBXKOCAMOOS-UHFFFAOYSA-N 0.000 description 1
- 238000011197 physicochemical method Methods 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
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- 229920002857 polybutadiene Polymers 0.000 description 1
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- 239000009719 polyimide resin Substances 0.000 description 1
- 229920005596 polymer binder Polymers 0.000 description 1
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- 238000006116 polymerization reaction Methods 0.000 description 1
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- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920003225 polyurethane elastomer Polymers 0.000 description 1
- 229920001289 polyvinyl ether Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000003908 quality control method Methods 0.000 description 1
- 229920013730 reactive polymer Polymers 0.000 description 1
- 229910052703 rhodium Inorganic materials 0.000 description 1
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- 239000002356 single layer Substances 0.000 description 1
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- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
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- 229910052726 zirconium Inorganic materials 0.000 description 1
Landscapes
- Non-Insulated Conductors (AREA)
- Conductive Materials (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〕
本発明は回路の接続に用いられる導電性の接続部材に関
する。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a conductive connecting member used for connecting circuits.
従来より集積回路類の配線基板への接続、表示素子類と
配線基板への接続、電気回路とリードとの接続などのよ
うに接続端子が細かいピッチで並んでいる場合の接続方
法として、ハンダ付や導電性接着剤による方法が広く用
いられている。しかしながら、これらの方法において&
了導電回路部のみに限定して接続部材を形成しなければ
ならないので、高密度、高精細化の進む微細回路の接続
に困難をきたしていた。Soldering has traditionally been used as a connection method when connecting terminals are lined up at a fine pitch, such as connecting integrated circuits to wiring boards, connecting display elements to wiring boards, and connecting electrical circuits to leads. Methods using conductive adhesives and conductive adhesives are widely used. However, in these methods &
Since the connecting member must be formed only in the conductive circuit portion, it has been difficult to connect fine circuits that are becoming increasingly dense and precise.
最近回路接続用の接続部材について恢肘が加えられ、す
でに特開昭51−20941号公報、特開昭55−10
4007号公報、%開昭56−122195号公報、特
開昭51−21192号公報等により提案されている。Recently, improvements have been made to connection members for circuit connections, and they have already been published in Japanese Patent Application Laid-Open No. 51-20941 and Japanese Patent Application Laid-Open No. 55-10.
This method has been proposed in Japanese Patent Application Laid-Open No. 4007, Japanese Patent Application Laid-Open No. 56-122195, Japanese Patent Application Laid-Open No. 51-21192, and the like.
これらにいずれもその基本思想は、相対峙する回路間に
導電性材料を含む異方導電性の接続部材層を設げ、加圧
または加熱加圧手段を構じることによって、回路間の電
気的接続と同時に隣接回路間に絶縁性を付与し相対峙す
る回路kW看固定するものである。The basic idea behind all of these is to provide an anisotropically conductive connecting member layer containing a conductive material between opposing circuits, and to apply pressure or heat and pressure means to generate electricity between the circuits. At the same time as the electrical connection, insulation is provided between adjacent circuits, and the kW of opposing circuits is fixed.
しかしながらこのような従来の方法において&了1回路
間の導通は主として複数個の導電性材料、多くの場合に
は金属粒子の接触によって得られるものであり、金属粒
子が141I直である為。However, in such conventional methods, conduction between circuits is mainly obtained by contact between a plurality of conductive materials, often metal particles, and the metal particles are directly connected.
粒子/′8子間あるいはいま一歩導通の信頼性が不足し
ていた。There was a lack of reliability in conduction between particles and particles.
また、特開昭58−111202号公報には導電性充て
ん剤を含むプラスチックを粉砕して粒子状とし、それを
導電粒子として用いる接続材料が記載されているがこの
方法ではグラスチック粒子が多量の導電性材料で充てん
される必要があシそれがために粒子が剛直化し、プジス
テック本来の熱軟化特注や柔軟性が損われ、さらには導
ii性そのものが低く、本発明の目的とする高信頼性接
続材料としては不適である。In addition, JP-A-58-111202 describes a connection material in which plastic containing a conductive filler is crushed into particles and used as conductive particles, but this method uses a large amount of plastic particles. The particles need to be filled with a conductive material, which makes the particles rigid, impairing Pusistek's original thermal softening and flexibility, and furthermore, the conductivity itself is low, making it difficult to achieve the high reliability that is the objective of the present invention. It is unsuitable as a sexual connection material.
本発明者らは先に回路接続用に極めて良好な透明性を有
する導電性接着シートを提案したがさらに上記欠点を改
善し、信頼性の高い接続を可能とする方法について鋭意
検討の結果、本発明に達した。The present inventors had previously proposed a conductive adhesive sheet with extremely good transparency for circuit connections, but as a result of intensive study on a method to improve the above-mentioned drawbacks and enable highly reliable connections, the present invention was developed. Achieved invention.
本発明は簡便な接着作業によp信y4性にすぐれた異方
導電接続を得ることの可能な微細回路接続用の接続部材
を提供せんとするもの゛ある。It is an object of the present invention to provide a connecting member for connecting fine circuits, which is capable of obtaining an anisotropically conductive connection with excellent p-reliability through a simple bonding operation.
すなわち本発明は、接着剤成分と導電性粒子とよりなる
接続部材において、導電性粒子として熱硬化性粒子から
なる核材(以下熱硬化性核材という)のほゞ全表面を金
R薄層により被覆した粒子を使用することt−%徴とす
る接続部材であり、好ましくは前記被積層を有する4電
性粒子は平均粒径が1〜50μmであり、粒子の最大径
に対する最小径の比が0.5〜1.0であり接続部材中
K(1,1〜10体積%官有され、かつ全光線透過率4
0%以上の透明性と感熱貼付性を有する接続部材である
。That is, the present invention provides a connecting member comprising an adhesive component and conductive particles, in which substantially the entire surface of a core material comprising thermosetting particles as conductive particles (hereinafter referred to as thermosetting core material) is coated with a gold R thin layer. Preferably, the laminated tetraelectric particles have an average particle diameter of 1 to 50 μm, and the ratio of the minimum diameter to the maximum diameter of the particles is 1 to 50 μm. is 0.5 to 1.0, K (1,1 to 10% by volume is present in the connecting member, and the total light transmittance is 4
This is a connecting member that has transparency of 0% or more and heat-sensitive adhesive properties.
本発明にか〜る接続部材においては、熱硬化性核材に被
Sされた金桶は接続時の加熱あるいは加熱加圧により、
導電性粒子相互あるいは導電回路部と接触して導通路を
形成するため信頼性に優れた微細回路の接続が可能とな
夛、さらには熱硬化性核材は加熱あるいは加熱加圧によ
る接続操作時K、若干の熱軟化性により導電回路に沿っ
た形で押付けるように変形し、それに伴い被覆された金
属は回路との接触面積が増大することから特に優れた導
電性を得ることができる。あわせて導電性粒子として、
極めて少量の金1−用いれば良いので、接続部材の軽量
化と貴重な金属の省資源化を提供するものである。In the connecting member according to the present invention, the metal tube coated with the thermosetting core material is heated or heated and pressurized at the time of connection.
Because the conductive particles come into contact with each other or with the conductive circuit to form a conductive path, it is possible to connect fine circuits with excellent reliability.Furthermore, the thermosetting core material can be used during connection operations by heating or heating and pressurizing. K. Due to its slight thermal softening property, it deforms so as to be pressed along the conductive circuit, and as a result, the coated metal has an increased contact area with the circuit, so that particularly excellent conductivity can be obtained. In addition, as conductive particles,
Since only a very small amount of gold 1 is required, it is possible to reduce the weight of the connecting member and save valuable metal resources.
また感熱貼付性を有する接着剤は、接続時の加熱あるい
は加熱加圧にエフ妥漕性七発境する為に、絶縁回路部に
おいても同時に機械的接続が行なえる。Furthermore, since adhesives having heat-sensitive adhesion properties are resistant to heating or heating and pressure during connection, mechanical connections can be made at the same time in insulated circuit parts.
さらに本発明になる接続部材は、導1を性粒子の核が熱
硬化性樹脂であるため、接続時の加熱あるいは加熱加圧
により、回路間において完全九流動することなく適当に
軟化変形し回路との接触面積を大きく保つことができる
。Furthermore, in the connecting member of the present invention, since the core of the conductor particles is a thermosetting resin, when heated or heated and pressurized during connection, the connecting member can be appropriately softened and deformed without completely flowing between the circuits. It is possible to maintain a large contact area with the
一方、絶縁回路部における粒子には、回路間の粒子はど
には圧力がかへらない為、隣接回路とのP、R性は充分
に得られる。On the other hand, since no pressure is applied to the particles in the insulated circuit section between the circuits, sufficient P and R properties can be obtained with respect to the adjacent circuits.
本発明にかかる接続部材の構成を図面と用いて更に詳し
く説明すると、第1図および第2図は本発明に使用する
導電性粒子を示す模式断面図であり、第1図においては
熱硬化性核材1の表面が金属層2で被覆されている様子
を示したものであり、−i″た第2図においては熱硬化
性核材1が中空部5.有する場合を示している。To explain the structure of the connecting member according to the present invention in more detail with reference to the drawings, FIGS. 1 and 2 are schematic cross-sectional views showing conductive particles used in the present invention, and in FIG. This figure shows how the surface of the core material 1 is covered with the metal layer 2, and the thermosetting core material 1 has a hollow portion 5 in FIG.
本発明の熱硬化性核材は第1図あるいは第2図の構成の
ものが単独あるいは混合して使用される。The thermosetting core material of the present invention having the structure shown in FIG. 1 or 2 can be used alone or in combination.
ここで核材とは、完全な充填体、内部が気体からなる中
空体、あるいは内部に若干の気泡部を含む発泡体など種
々の構成をとることかできる。Here, the core material can have various configurations, such as a completely filled body, a hollow body whose interior is made of gas, or a foam body containing some air bubbles inside.
また核材1は金JA 2により全面被覆されているのが
最適であるが、一部の未核6部があってもさしつかえな
い。熱硬化性核材1の形状ははy球状であることが好ま
しいが1表面に突起や凹凸があっても良い。また核材粒
子が凝集した凝集体としても使用できる。Further, it is optimal that the core material 1 is entirely covered with gold JA 2, but there may be some unnucleated portion 6. The thermosetting core material 1 preferably has a spherical shape, but may have protrusions or irregularities on one surface. It can also be used as an aggregate of core material particles.
本発明で用いられる熱硬化性核材1としては、たとえば
尿素、エチレン−尿素、メラミン、ペンソクアナミン、
フェノール−ホルマリン、レゾルシノール−ホルムアル
デヒド、キシレン。Examples of the thermosetting core material 1 used in the present invention include urea, ethylene-urea, melamine, pensoquanamine,
Phenol-formalin, resorcinol-formaldehyde, xylene.
フラン、ジアリルフタレート、エポキシ、ポリイソシア
ネート、ポリイミド、ポリエステル、アクリル、ベンズ
イミダゾール%フェノキシ、フッ素、シリコーンなどの
各樹脂が適用可能であり、接続部材の作製に支障のない
範囲であればその硬化度合は問わないものとし、これら
の単体や2種以上の複合物か用いられる。また核材とし
て、反応性ポリマーブレンドとして知られる例えばエポ
キシ樹脂やフェノ−h樹脂などの前記各樹脂類とナイロ
ン、ポリアミド、ポリ丈ル7アイド、ニトリルゴム等の
合成ゴム、などの単体および複合物とのブレンドも可能
である。Resins such as furan, diallyl phthalate, epoxy, polyisocyanate, polyimide, polyester, acrylic, benzimidazole% phenoxy, fluorine, and silicone are applicable, and the degree of curing is within the range that does not interfere with the production of the connecting member. Any single substance or a combination of two or more of these may be used. In addition, as a core material, single or composite materials such as reactive polymer blends, such as the above-mentioned resins such as epoxy resin and phenol-h resin, and synthetic rubbers such as nylon, polyamide, polyurethane rubber, and nitrile rubber, may be used. It is also possible to blend with
さらに自己型@注あるいは、カルボン酸基、エポキシ基
、アミノ基、ヒドロキシル基などの重付性官能基を有す
る各樹脂類も単独あるいは複合して、さらに架橋剤硬化
剤等と併用して用いることもできる。Furthermore, resins with self-type @Note or heavy functional groups such as carboxylic acid groups, epoxy groups, amino groups, and hydroxyl groups can be used alone or in combination, and in combination with crosslinking agents, curing agents, etc. You can also do it.
被αに用いられる金属2としてはAI、 Sb、Be。The metal 2 used for α is AI, Sb, and Be.
Bi、 Cd、 Ca、 Cs、 Cr、 Co、 C
u、 Ce、 Au、 lr、Fe。Bi, Cd, Ca, Cs, Cr, Co, C
u, Ce, Au, lr, Fe.
Pb、 L4. Mg、 Mn、 Hg、 Mo、 N
i、 Pd、 Pt、 K、 Rh。Pb, L4. Mg, Mn, Hg, Mo, N
i, Pd, Pt, K, Rh.
Se、 Si、 Ag、 Na、 Sr、 Ta、 S
n、 TI、 W、 U、 V+Y、 Zn、 Zr、
TI、 As、 In、 Luなどの導電性を有する
金属が適用可能でありこれらの単体あるいは酸化物など
でも良く281以上複合して用いるか、あるいは又2種
以上の合金などでありでも良い。Se, Si, Ag, Na, Sr, Ta, S
n, TI, W, U, V+Y, Zn, Zr,
Conductive metals such as TI, As, In, and Lu can be used, and these metals may be used alone or as oxides, or in a combination of 281 or more, or as an alloy of two or more types.
熱硬化性核材1の表面上に金Jf42を形成する方法と
しては、たとえば蒸着法、スパッタリング法、メッキ法
などの物理化学的方法や、熱硬化性核材の会成時に少量
の金PA′にモノマー中に分散させ、重合後のポリマー
粒子表面に金属粉を吸着させたシ、官能i&を有する核
材と金属を化学結付させたり、果面活性剤やカップリン
グ剤などにより吸着させるなどの化学的手法による等の
方法が採用できる、また被榎膚の厚みは任意に設定でき
る。Methods for forming gold Jf42 on the surface of the thermosetting core material 1 include, for example, physicochemical methods such as vapor deposition, sputtering, and plating, or using a small amount of gold PA' at the time of forming the thermosetting core material. The metal powder is dispersed in a monomer and adsorbed onto the surface of the polymer particles after polymerization, the metal is chemically bonded to the core material having functional i&, or the metal is adsorbed with a surface activator or a coupling agent, etc. The thickness of the exposed skin can be set arbitrarily.
従来このような4通粒子として、ガラス球(ビーズ)あ
るいはガラス中空球(バルーン)にAg等の薄ノーを設
けたものもあるが、これらのガラス球あるいは中空球は
、加熱加圧時に軟化変形することが出来ない為、本発明
の実施には不適である。Conventionally, such four-round particles have been made by providing thin holes such as Ag on glass spheres (beads) or glass hollow spheres (balloons), but these glass spheres or hollow spheres soften and deform when heated and pressurized. Therefore, it is not suitable for implementing the present invention.
上記により得られた導電性粒子は平均粒径が1〜50μ
m、粒子径の最大径に対する最小径の比が0.5へ1.
0であるものとする。粒子径が1μm以下では多量の導
電性粒子を必要とし、また結果的に充填粒子量が多くな
るため接着力の低下が大きく、50μm以上になると、
粒子が大きく隣接回路間(スペース部)が導通されるよ
うになる為好ましくない。The conductive particles obtained above have an average particle size of 1 to 50μ
m, the ratio of the minimum diameter to the maximum diameter of the particles is 0.5 to 1.
Assume that it is 0. When the particle size is 1 μm or less, a large amount of conductive particles is required, and as a result, the amount of packed particles increases, resulting in a large decrease in adhesive strength, and when the particle size is 50 μm or more,
This is not preferable because the particles are large and cause electrical conduction between adjacent circuits (space parts).
4電性粒子の形状については、前記の如く最大径に対す
る最小径の比(以下粒径比ンが0.5〜1.08度とす
る。この範囲外では、粒子があまりにもフレーク状にな
り、本発明の目的とする回路間の導電性と隣接回路間の
絶縁性を得るには不向きになるし、また回路間の接lf
t注も低下する傾向が強くなる。この範囲金満たす例と
しては、はg球状であるものが代表的であるが、上記の
条件を満たすものであれば特に限定さ扛ない。また粒子
表面に突起物や凹凸があっても良い。また単一粒子に限
定されず凝集体からなる粒子であっても良い。Regarding the shape of the tetraelectric particles, as mentioned above, the ratio of the minimum diameter to the maximum diameter (hereinafter, the particle size ratio is defined as 0.5 to 1.08 degrees. Outside this range, the particles become too flaky). , it becomes unsuitable for obtaining the electrical conductivity between circuits and the insulation between adjacent circuits, which are the objects of the present invention, and the connection between circuits lf.
There is also a strong tendency for t-notes to decrease. A typical example that satisfies this range is a spherical shape, but there is no particular limitation as long as it satisfies the above conditions. Further, the particle surface may have protrusions or irregularities. Further, the particles are not limited to single particles, but may be particles made of aggregates.
また粒子径は全体的な平均粒径をとるものとし、粒子の
形状や粒子径の測定は、たとえば走査形電子顕微鏡など
による方法が便利である。Further, the particle size is assumed to be the overall average particle size, and it is convenient to measure the particle shape and particle size using, for example, a scanning electron microscope.
導電性粒子が球状であると、接続時の加熱加圧により粒
子相互あるいは粒子と回路面との接触を得やすく高導電
性を得やすい。When the conductive particles are spherical, it is easy to obtain contact between the particles or between the particles and the circuit surface by applying heat and pressure during connection, and it is easy to obtain high conductivity.
導電性粒子は接続部材の厚み方向に単層で存在しても良
いし、厚み方向に複数個配列した構造であっても良い。The conductive particles may exist in a single layer in the thickness direction of the connection member, or may have a structure in which a plurality of conductive particles are arranged in the thickness direction.
接着剤中に占める4を性粒子は0.1へ10体積%が過
半である。0.1体積%以下では満足する導電性が得ら
れず、10体積%以上では隣接回路との絶縁性が低下し
接続部材の透明性も得られない。The majority of the 4-carbon particles in the adhesive are 0.1 to 10% by volume. If it is less than 0.1% by volume, satisfactory conductivity cannot be obtained, and if it is more than 10% by volume, the insulation with adjacent circuits decreases and transparency of the connecting member cannot be obtained.
本発明で用いられる接着剤としては、基本的には絶縁性
を示す通常の接着性シート類罠用いられている配合が適
用可能である。通常の接滑シート類に用いられる配合は
凝集力を付与するポリマーと、その他必賛に応じて用い
る粘着付与剤、粘着性調整剤、架橋剤、老化防止剤、分
散剤等からなっている。As the adhesive used in the present invention, basically any formulation used in ordinary adhesive sheets exhibiting insulation properties can be used. The formulation used for ordinary sliding sheets consists of a polymer that imparts cohesive force, and other components such as tackifiers, tackifiers, crosslinkers, anti-aging agents, and dispersants, which are used as required.
これらポリマー徨としては、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iu物、 ポリエチ
レン、エチレン−プロピレン共重合体、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、ポリイノブチレン、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−ニトリル−ブ
タジェン共重合体、スチレンーブタジヱンブロック共重
合体、スチレン−イン7’レンブロック共重曾体、ポリ
ブタジェン、エチレンセルロース、ポリエステル、エポ
キシ、ポリアミド、ポリウレタン、天然ゴム、シリコン
系ゴム、ポリクロロプレン等の会成ゴム類、ポリビニル
エーテルなどが適用可能であり、単独あるい警工2種以
上併用して用いられる。These polymers include ethylene vinyl acetate copolymer, ethylene-vinyl acetate copolymer IU, polyethylene, ethylene-propylene copolymer, ethylene-acrylic acid copolymer, ethylene-acrylic acid ester copolymer, ethylene - Acrylate copolymer, acrylic ester rubber, polyinobutylene, atactic polypropylene, polyvinyl butyral, acryl-nitrile-butadiene copolymer, styrene-butadiene block copolymer, styrene-yne 7' Synthetic rubbers such as Renblock copolymer, polybutadiene, ethylene cellulose, polyester, epoxy, polyamide, polyurethane, natural rubber, silicone rubber, polychloroprene, polyvinyl ether, etc. can be used alone or as a Two or more types are used in combination.
粘着付与剤としては、ジシクロペンタジェン4t4脂、
ロジン、変性ロジン、テルペン樹脂、キシレンff4
脂、テルペン−フェノール樹脂、アル中ルフェノール樹
脂、 クマロン−インデン樹脂等があり、これらを必要
に応じて、単独あるいは2種以上併用して用いる。粘着
性調整剤としてはたとえばジオクチルフタレートにはじ
めとする各種可塑剤類等が代表的である。As a tackifier, dicyclopentadiene 4t4 fat,
Rosin, modified rosin, terpene resin, xylene ff4
There are resins, terpene-phenol resins, alcohol-based phenol resins, coumaron-indene resins, etc., and these may be used alone or in combination of two or more, if necessary. Typical tackiness modifiers include various plasticizers such as dioctyl phthalate.
架橋剤はポリマーの凝集力を高めることが必要な場合に
用いらn、ポリマの官能基と反応する多官能性物質であ
り、たとえばポリイソシアネート、メラミン樹脂、尿素
@脂、フェノール樹脂等があげられる。Crosslinking agents are used when it is necessary to increase the cohesive force of polymers, and are polyfunctional substances that react with the functional groups of polymers, such as polyisocyanates, melamine resins, urea@fats, phenolic resins, etc. .
老化防止剤は、ポリマーバインダの熱、酸素、光等に対
する安定性を高めることが必要な場合に用いるものでた
とえば金属石ケン類を代表とする安定剤や、アルキルフ
ェノール類などの酸化防止41.ベンゾフェノン系、ベ
ンゾトリアゾール系などの紫外線吸収剤等があり、やは
り必要に応じて単独あるいは2種以上併用して用いらn
る。Antioxidants are used when it is necessary to increase the stability of the polymer binder against heat, oxygen, light, etc., and include stabilizers such as metal soaps and antioxidants such as alkylphenols. There are UV absorbers such as benzophenone type and benzotriazole type, and they can be used alone or in combination of two or more as necessary.
Ru.
分散剤は、導電性粒子の分散性向上のために用いる場合
がある。この例としてはたとえば界面活性剤がありノニ
オン糸、カチオン系、アニオン系、両性のうち1種ある
いは2種以上併用して用いることができる。A dispersant may be used to improve the dispersibility of conductive particles. Examples of this include surfactants, which can be used in combination of one or more of nonionic, cationic, anionic, and amphoteric surfactants.
本発明にか又る接続部材の製造方法としては、ポリマお
よびその他必要に応じて使用する添加剤からなる従N剤
組成物を溶剤に溶解するか懸濁状に媒体中に分散しある
いは熱浴融させて液状とした後に導電性粒子をボールミ
ルなどの通常の方法により混合し、導電性粒子混合接着
剤組成物を得る。The method of manufacturing the connecting member according to the present invention includes dissolving a conventional N agent composition consisting of a polymer and other additives used as necessary in a solvent, dispersing it in a suspension state in a medium, or dispersing it in a hot bath. After melting to a liquid state, conductive particles are mixed by a conventional method such as a ball mill to obtain a conductive particle mixed adhesive composition.
溶剤を用いる場合については熱硬化性核材上に金属層の
形成された導電性粒子は溶剤に対する溶解性が減少して
いるため溶剤?用いることも可能であるが、接着剤全醪
解し熱硬化性核材を溶解しない溶剤全選択することがさ
らに好ましい。この手段としては、たとえば接着剤をエ
マルシラン化して水媒体中に導電性粒子を分散すること
もよい方法である。When using a solvent, conductive particles with a metal layer formed on a thermosetting core material have reduced solubility in solvents. Although it is possible to use a solvent, it is more preferable to select a solvent that completely melts the adhesive and does not dissolve the thermosetting core material. A good method for this purpose is, for example, to emulsify the adhesive and disperse the conductive particles in an aqueous medium.
上記導電性粒子混合接着剤は、接続を要する一方あるい
は双方の回路上にスクリーン印刷やロールコータ等の手
段?用いて直接回路上に接続部材Nを形成しても良い。Is the above conductive particle mixed adhesive applied to one or both circuits that require connection by means such as screen printing or roll coating? The connecting member N may be formed directly on the circuit using the above-mentioned method.
また接続部材の連続長尺体を回路上に施しても良い。こ
の場合接続部材の連続長尺体を得るには紙やプラスチッ
クフィルム等に必要に応じて剥離処理を行なったセパレ
ータ上に前記手段により接続部材層を形成後巻重しても
良いし、接N層の粘M注が蕪い場合においてはセパレー
タを用いずに巻重することも可能である。Further, a continuous elongated body of the connecting member may be provided on the circuit. In this case, in order to obtain a continuous long body of the connecting member, the connecting member layer may be formed by the above method on a separator made of paper or plastic film, which has been subjected to peeling treatment as necessary, and then rolled up. If the viscosity of the layers is low, it is also possible to overlap the layers without using a separator.
上記製法において接着剤組成物中に浴剤あるいは分散媒
を含む場合においては溶剤乾燥時の厚み方向の体積収縮
現象全利用して導電性粒子が厚み方向により密な配列を
有する接続部材を得ることが可能であり、又無浴剤下の
ホットメルト塗工においては、製造時の溶剤による環境
汚染を防止することができる。In the above manufacturing method, when the adhesive composition contains a bath agent or a dispersion medium, the volume shrinkage phenomenon in the thickness direction during drying of the solvent is fully utilized to obtain a connecting member in which the conductive particles are arranged more densely in the thickness direction. In addition, in hot-melt coating without a bath agent, environmental pollution caused by solvents during production can be prevented.
接続部材層の厚みは、導電性粒子の粒径および接続部材
の特性を考慮して相対的に決定するが、5へ100μm
の厚みが好ましい。The thickness of the connecting member layer is relatively determined taking into account the particle size of the conductive particles and the characteristics of the connecting member, but it is between 5 and 100 μm.
A thickness of .
5um以下では光分な接着性が得られず、100μm以
上では充分な導電性を得る為に多量の4電性粒子の混合
を必安とすることから実用的でない。If the thickness is less than 5 um, optical adhesion cannot be obtained, and if it is 100 μm or more, a large amount of tetraelectric particles must be mixed in order to obtain sufficient conductivity, which is not practical.
得られた接続部材面は、必要に応じて塵埃等の付着防止
のためにセパレータで【りても良いし、あるいは両面セ
パレータを用いれば連続的に巻重することも可能である
◎
このようにして得られた接続部材はかなりの透明性を有
する。接続部材が透明性を有すると製造時の品質管理が
行い易く外観上の見映えも良い。また表示素子類の接着
等においては、級着体を透視できる構成をとることが可
能となる。The obtained connecting member surface may be covered with a separator to prevent the adhesion of dust, etc., if necessary, or it may be possible to continuously roll the material using a double-sided separator. The resulting connecting member has considerable transparency. When the connecting member is transparent, quality control during manufacturing is easy to perform and the appearance is good. In addition, when adhering display elements, etc., it becomes possible to adopt a configuration in which the adhesive body can be seen through.
得られた接続部材を用いて回路を接着する方法としては
、たとえば回路にフィルム状接続部材を仮貼付した状態
でセパレータのある場付にはセパレータを剥離し、ある
いは導電性接着剤組成物を塗布し必要に応じて溶剤除去
後の状態でその面に回路5を熱プレスあるいは加熱ロー
ル等で貼付ければよい。A method for bonding a circuit using the obtained connecting member is, for example, by temporarily attaching a film-like connecting member to the circuit, and then peeling off the separator at the place where the separator is located, or applying a conductive adhesive composition. If necessary, the circuit 5 may be attached to the surface after removing the solvent using a hot press or a heated roll.
第5図および第4歯はか〜る方法により回路を接続した
状態を模式的に示したもので、熱と圧力によりて巌着剤
4が軟化流動するとともに導電性粒子8も軟化変形し相
互に接触するので両回路5,6間の導通接着が可能とな
る。FIG. 5 and the fourth tooth schematically show the state in which the circuit is connected by the above method, and as the adhesive 4 softens and flows due to heat and pressure, the conductive particles 8 also soften and deform, and mutually interact with each other. Since the two circuits 5 and 6 are in contact with each other, conductive adhesion between the two circuits 5 and 6 becomes possible.
第6因は回路5,6間に導電性粒子8が複層ないしそれ
以上存在する場せの例で粒子表面の金属層同士で接触し
て導電路を形成するので高専1!注が得られる。The sixth factor is an example where there are multiple or more layers of conductive particles 8 between the circuits 5 and 6, and the metal layers on the surface of the particles contact each other to form a conductive path. Notes are obtained.
接続時の加熱加圧に際し、被覆金属は薄層であるために
PJ@化性核材の変形に充分追随可能であり、もしや変
形に追随できずに金PA/Ilにヒビ割れ等の欠陥が生
じても、回路あるいは、他の粒子との接触により導電路
は保持できる。During heating and pressurization during connection, the coating metal is a thin layer, so it can sufficiently follow the deformation of the PJ@-formable core material, and if it cannot follow the deformation, defects such as cracks will occur in the gold PA/Il. Even if this occurs, the conductive path can be maintained by contact with the circuit or other particles.
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.
実施例1〜6
(1)接続部材の佳辰
表面をAuで被覆されたエポキシ樹脂球状粒子を、贋チ
レンブタジエンブロック共重合体(M12.6)100
部と軟化点120℃のテルペン系粘着付与剤40部およ
びトルエン200部よりなる接着剤溶液中に象加皿を変
えて配付した。Examples 1 to 6 (1) Epoxy resin spherical particles of which the surface of the connection member was coated with Au were coated with 100% of fake ethylene butadiene block copolymer (M12.6).
The samples were placed in an adhesive solution containing 40 parts of a terpene-based tackifier having a softening point of 120° C. and 200 parts of toluene using different inlaid plates.
上記配付物を超音波分散して、導電性粒子混合の接着剤
溶液を得た。The above handout was subjected to ultrasonic dispersion to obtain an adhesive solution containing conductive particles.
このM Q k バーコータでセパレータ(シリコーン
処理ポリエステルフィルム)上に塗布し、100℃−5
分の乾燥を行ない浴剤を除去してフィルム状の接続部材
を得た。Coated on a separator (silicone-treated polyester film) with this MQk bar coater and heated at 100℃-5
After drying for a few minutes and removing the bath agent, a film-like connection member was obtained.
(2) 評1曲
ライン巾(l1mm、ピッチ0.2[nLllの回路を
有する全回路幅IQQmmのフレキシブル回路板(FP
C)に、接着中3 mm、長さ1QQmm[切断した上
記接続部材を載置して100℃−10kg/an’−s
秒の加熱加圧により仮貼付して接続部材付FPCを得た
。(2) Evaluation A flexible circuit board (FP) with a total circuit width of IQQmm and a circuit with a line width of one track (l1mm) and a pitch of 0.2[nLll].
C), 3 mm during adhesion, length 1 QQ mm [The cut connection member was placed and heated at 100°C - 10 kg/an'-s.
Temporary attachment was performed by heating and pressurizing for seconds to obtain an FPC with connection members.
そのあとセパレータ全剥離して、他の同一ピッチを有す
るFPCiセパレータ剥離而に載面て顕微鏡でFPC回
路の位置合せをした後、圧力15kg/an”で10秒
間加熱加圧して回路を接続した。接層温度は第1表に示
すとおりでありプレスの熱板温度を調節して求めた。各
実施例において接着シートは透明性を有している1こめ
、透過光の助けにより回路の位置会せが容易であった。Thereafter, the separator was completely peeled off, placed on another peeled FPCi separator having the same pitch, and the FPC circuit was aligned using a microscope, and the circuit was connected by heating and pressurizing at a pressure of 15 kg/an'' for 10 seconds. The contact layer temperature is as shown in Table 1 and was determined by adjusting the temperature of the hot plate of the press.In each example, the adhesive sheet was transparent. It was easy to set up.
%注を第1表に示したが、各実施例において良好なるS
a低抵抗よび隣接回路との絶縁性を示した。また受@条
件の広い範囲で良好な結果をえた。The percentages are shown in Table 1, and each example shows good S.
a Shows low resistance and insulation from adjacent circuits. Good results were also obtained under a wide range of acceptance conditions.
比較例−1
実施例1〜6と同様に接続部材を作成評価したが、導電
性粒子の箔加量を20体8R%と増量した。この場合、
全先勝?L過率が低下し、回路の位噴台せが困難であり
、また隣接回路との絶縁性が不足した。Comparative Example 1 A connecting member was prepared and evaluated in the same manner as in Examples 1 to 6, but the amount of conductive particles in the foil was increased to 20 pieces and 8R%. in this case,
All first wins? The L pass rate decreased, it was difficult to position the circuit, and the insulation from adjacent circuits was insufficient.
比較例−2
実施例1〜6と同様であるが、導電性粒子としてアトマ
イズ法で得た粒径45μmのニッケル粒子を用いた。こ
の場合、初期の抵抗は良好であるが、信頼性試験の評価
で導通不良が発生した。Comparative Example 2 This was the same as Examples 1 to 6, but nickel particles with a particle size of 45 μm obtained by the atomization method were used as the conductive particles. In this case, although the initial resistance was good, a continuity failure occurred in the reliability test evaluation.
実施例−7
表面をNi で被校されたポリイミド樹脂球状粒子を
熱oT塑性ポリエステル樹脂(分子量約20.0OC1
,ガラス転移温度7℃)の30%メチルエテルケトン溶
液中に分散混合して導′邂注粒子混合接着剤溶液全作製
し、実施例1″−6と同様にしてフィルム状接続部材を
得た。前記実施例1〜6と同様に接続部材付FPCを得
た後に同ピツチの回路を有する透明導電ガラスに貼合せ
て評価した結果を第1表に示すが、良好な特性を有して
いた。Example 7 Polyimide resin spherical particles coated with Ni on the surface were heated to thermoplastic polyester resin (molecular weight approximately 20.0OC1).
, a glass transition temperature of 7° C.) was dispersed and mixed in a 30% methyl ether ketone solution to prepare a total adhesive solution containing particles, and a film-like connecting member was obtained in the same manner as in Example 1''-6. Table 1 shows the results of evaluation after obtaining an FPC with a connecting member in the same manner as in Examples 1 to 6 and pasting it on transparent conductive glass having a circuit of the same pitch. .
実施例−8
実施例−7で得た4電柱粒子混合接着剤溶液を、セパレ
ータ上でな(、FPCの回路上にIK従塗布乾燥して接
続部材付FPCを得た。Example 8 The four electric pole particle mixed adhesive solution obtained in Example 7 was applied on a separator (IK) onto the circuit of the FPC and dried to obtain an FPC with a connecting member.
その後、実施例7と同様に、同ピツチの回路を有する透
明ガラス電極と貼付せて同様な評価を行なった結果を第
1表に示す。実施例−7と同様に良好な初期特注および
信頼性を得た。Thereafter, in the same manner as in Example 7, a transparent glass electrode having a circuit of the same pitch was attached and the same evaluation was performed.Table 1 shows the results. As in Example 7, good initial customization and reliability were obtained.
第1表において
(1)導通抵抗は、接続部材により接続した2枚の回路
の対向電極間の抵抗をマルチメータにて測定(接続面m
0.1mraX3m+n)(2)絶縁抵抗は、接続部材
によシjM続した2枚の回路の隣接回路間の抵抗をハイ
メグオームメータにて測定
(6)信頼性は、接続部材により接続した2枚の回路t
−−20℃・50分/80℃・60分の熱衝撃を1サイ
クルとして100サイクル処理し、その後の導通抵抗全
測定して評価した。In Table 1, (1) Continuity resistance is measured by using a multimeter to measure the resistance between opposing electrodes of two circuits connected by a connecting member (connection surface m
0.1mraX3m+n) (2) Insulation resistance is measured by measuring the resistance between adjacent circuits of two circuits connected by a connecting member using a high-megohmmeter (6) Reliability is measured by measuring the resistance between two circuits connected by a connecting member. The circuit t
--Thermal shock at 20° C. for 50 minutes/80° C. for 60 minutes was treated for 100 cycles, and the conduction resistance was then completely measured for evaluation.
(4) 全光線透過率はJIS K−6714に準
拠して日本電色工莱(相製デジタル濁度計NDH−20
Dにより測定した。(4) Total light transmittance was measured using Nippon Denshoku Korai (Aisaku Digital Turbidity Meter NDH-20) in accordance with JIS K-6714.
Measured by D.
以上詳述したように本発明になる接続部材は熱硬化性核
材の表面に導電性を有する金属薄層を形成した導電性粒
子を用いることにより、回路接続時の条件中が広くなt
)接続作業性が向上し、接続後の温度変化に対して侶穎
注が著しく向上した。As detailed above, the connecting member of the present invention uses conductive particles with a conductive metal thin layer formed on the surface of a thermosetting core material, thereby allowing a wide variety of circuit connection conditions.
) Connection workability has been improved, and resistance to temperature changes after connection has been significantly improved.
また隣接回路との絶縁性が充分に得らnるので微細回路
用の接続材料として有用である〇さらに接続部材は透明
性を有しているので微細回路の位置会わせを透過光の助
けをかりて簡単に行なえるなどの利点を有する。It also provides sufficient insulation from adjacent circuits, making it useful as a connecting material for fine circuits.Furthermore, since the connecting material is transparent, it is possible to align fine circuits with the help of transmitted light. It has the advantage of being easy to perform.
第1図および@2図は導を性粒子の僕式断面必。第6図
および第4図は本発明に係る接続部材を用いて回路接続
した状態を示す模式断面図。
符号の説明
1 熱硬化性核材 2 金属
5 中空部 4 接着剤
5 回路 6 回路
7 絶縁性基板 8411性粒子第4図
手続補正書(自発)
昭#。61年 8月25日Figures 1 and 2 show the cross-sections of conductive particles. FIG. 6 and FIG. 4 are schematic sectional views showing a state in which a circuit is connected using a connecting member according to the present invention. Explanation of symbols 1 Thermosetting core material 2 Metal 5 Hollow part 4 Adhesive 5 Circuit 6 Circuit 7 Insulating substrate 8411 Particulate Figure 4 Procedural Amendment (Spontaneous) Showa #. August 25, 1961
Claims (1)
において、前記導電性粒子が熱硬化性樹脂粒子からなる
核材のほゞ全表面を金属薄層により被覆された粒子であ
ることを特徴とする回路の接続部材。 2、導電性粒子の平均粒径が1〜50μm、粒子の最大
径に対する最小径の比が0.5〜1.0であり接続部材
中に0.1〜10体積%含有され、かつ全光線透過率(
JIS K−6714)が40%以上である特許請求の
範囲第1項記載の回路の接続部材。 3、接続部材が感熱貼付性を有するものてある特許請求
の範囲第1項または第2項記載の回路の接続部材。[Claims] 1. In a circuit connecting member comprising an adhesive component and conductive particles, the conductive particles cover substantially the entire surface of a core material consisting of thermosetting resin particles with a thin metal layer. A connection member for a circuit, characterized in that it is made of particles. 2. The average particle diameter of the conductive particles is 1 to 50 μm, the ratio of the minimum diameter to the maximum diameter of the particles is 0.5 to 1.0, and the connecting member contains 0.1 to 10% by volume, and the total light beam Transmittance (
JIS K-6714) is 40% or more, the circuit connecting member according to claim 1. 3. The circuit connecting member according to claim 1 or 2, wherein the connecting member has heat-sensitive adhesion properties.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP833286A JPS62165886A (en) | 1986-01-18 | 1986-01-18 | Jointing member of circuiy |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP833286A JPS62165886A (en) | 1986-01-18 | 1986-01-18 | Jointing member of circuiy |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS62165886A true JPS62165886A (en) | 1987-07-22 |
Family
ID=11690238
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP833286A Pending JPS62165886A (en) | 1986-01-18 | 1986-01-18 | Jointing member of circuiy |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS62165886A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6507594B1 (en) | 1997-09-30 | 2003-01-14 | Canon Kabushiki Kaisha | Optical device structure and fabrication method thereof |
-
1986
- 1986-01-18 JP JP833286A patent/JPS62165886A/en active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6507594B1 (en) | 1997-09-30 | 2003-01-14 | Canon Kabushiki Kaisha | Optical device structure and fabrication method thereof |
US6771677B2 (en) | 1997-09-30 | 2004-08-03 | Canon Kabushiki Kaisha | Optical device structure and fabrication method thereof |
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