JPH0146548B2 - - Google Patents
Info
- Publication number
- JPH0146548B2 JPH0146548B2 JP60296604A JP29660485A JPH0146548B2 JP H0146548 B2 JPH0146548 B2 JP H0146548B2 JP 60296604 A JP60296604 A JP 60296604A JP 29660485 A JP29660485 A JP 29660485A JP H0146548 B2 JPH0146548 B2 JP H0146548B2
- Authority
- JP
- Japan
- Prior art keywords
- parts
- weight
- adhesive
- resin
- adhesive tape
- 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.)
- Expired
Links
- 230000001070 adhesive effect Effects 0.000 claims description 28
- 239000002390 adhesive tape Substances 0.000 claims description 26
- 239000000853 adhesive Substances 0.000 claims description 22
- 239000011347 resin Substances 0.000 claims description 20
- 229920005989 resin Polymers 0.000 claims description 20
- 229920000578 graft copolymer Polymers 0.000 claims description 14
- 238000002844 melting Methods 0.000 claims description 13
- 229920000642 polymer Polymers 0.000 claims description 12
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 11
- 229920001577 copolymer Polymers 0.000 claims description 10
- 230000009477 glass transition Effects 0.000 claims description 9
- 230000008018 melting Effects 0.000 claims description 8
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 7
- 239000000178 monomer Substances 0.000 claims description 7
- 239000007795 chemical reaction product Substances 0.000 claims description 6
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 5
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 5
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 5
- -1 acrylic ester Chemical class 0.000 claims description 5
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Chemical compound C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 125000005396 acrylic acid ester group Chemical group 0.000 claims description 3
- 150000001735 carboxylic acids Chemical class 0.000 claims description 3
- 239000005011 phenolic resin Substances 0.000 claims description 3
- 239000008096 xylene Substances 0.000 claims description 3
- IANQTJSKSUMEQM-UHFFFAOYSA-N 1-benzofuran Chemical compound C1=CC=C2OC=CC2=C1 IANQTJSKSUMEQM-UHFFFAOYSA-N 0.000 claims description 2
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 claims 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 claims description 2
- 239000003822 epoxy resin Substances 0.000 claims description 2
- 229920000647 polyepoxide Polymers 0.000 claims description 2
- 150000003097 polyterpenes Chemical class 0.000 claims 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 claims description 2
- 150000007934 α,β-unsaturated carboxylic acids Chemical class 0.000 claims description 2
- 125000004185 ester group Chemical group 0.000 claims 1
- 239000004820 Pressure-sensitive adhesive Substances 0.000 description 16
- 239000010410 layer Substances 0.000 description 9
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 8
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 5
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 4
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 4
- WABPQHHGFIMREM-UHFFFAOYSA-N lead(0) Chemical group [Pb] WABPQHHGFIMREM-UHFFFAOYSA-N 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 229920001228 polyisocyanate Polymers 0.000 description 4
- 239000005056 polyisocyanate Substances 0.000 description 4
- 238000007665 sagging Methods 0.000 description 4
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 239000000470 constituent Substances 0.000 description 3
- 239000003999 initiator Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000000123 paper Substances 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical group CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- 230000004913 activation Effects 0.000 description 2
- 239000012790 adhesive layer Substances 0.000 description 2
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 239000002655 kraft paper Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 2
- 239000002985 plastic film Substances 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- 125000004200 2-methoxyethyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])* 0.000 description 1
- VFXXTYGQYWRHJP-UHFFFAOYSA-N 4,4'-azobis(4-cyanopentanoic acid) Chemical compound OC(=O)CCC(C)(C#N)N=NC(C)(CCC(O)=O)C#N VFXXTYGQYWRHJP-UHFFFAOYSA-N 0.000 description 1
- NQSLZEHVGKWKAY-UHFFFAOYSA-N 6-methylheptyl 2-methylprop-2-enoate Chemical compound CC(C)CCCCCOC(=O)C(C)=C NQSLZEHVGKWKAY-UHFFFAOYSA-N 0.000 description 1
- DXPPIEDUBFUSEZ-UHFFFAOYSA-N 6-methylheptyl prop-2-enoate Chemical compound CC(C)CCCCCOC(=O)C=C DXPPIEDUBFUSEZ-UHFFFAOYSA-N 0.000 description 1
- XFZOHDFQOOTHRH-UHFFFAOYSA-N 7-methyloctyl 2-methylprop-2-enoate Chemical compound CC(C)CCCCCCOC(=O)C(C)=C XFZOHDFQOOTHRH-UHFFFAOYSA-N 0.000 description 1
- CUXGDKOCSSIRKK-UHFFFAOYSA-N 7-methyloctyl prop-2-enoate Chemical compound CC(C)CCCCCCOC(=O)C=C CUXGDKOCSSIRKK-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- 229920005601 base polymer Polymers 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 238000012662 bulk polymerization Methods 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000012986 chain transfer agent Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000010556 emulsion polymerization method Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical compound CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 1
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 1
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 239000012943 hotmelt Substances 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- JDNTWHVOXJZDSN-UHFFFAOYSA-N iodoacetic acid Chemical compound OC(=O)CI JDNTWHVOXJZDSN-UHFFFAOYSA-N 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 125000005397 methacrylic acid ester group Chemical group 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 229920006255 plastic film Polymers 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 238000010558 suspension polymerization method Methods 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Supply And Installment Of Electrical Components (AREA)
- Adhesive Tapes (AREA)
- Adhesives Or Adhesive Processes (AREA)
Description
産業上の利用分野
本発明は、アクリル系グラフトポリマに熱溶融
性樹脂を配合してなる新規な熱時感圧性接着剤の
層を有してなり、リード線を介して電子部品をス
ダレ状の配列に連設保持するための接着テープに
関するものである。
従来の技術
リード線を接着テープと非接着テープとではさ
みつけるようにしてリード線付電子部品をスダレ
状の配列で連設保持し、その電子部品を回路基板
等の作製工程に自動的に供給する電子部品の自動
組入れシステムが知られている(実公昭43−
12368号公報)。すなわち、電子計算機による制御
下に、スダレ状配列の電子部品におけるリード線
の末端部を切断して連設状態を解きつつ、解かれ
た電子部品を順次自動的に作製工程に組入れて回
路基板等を組立る方法が知られている。この自動
組入れシステムにおいては電子部品は接着テープ
に高い精度でもつて等間隔にかつ平行に連設され
ていることが要求される。
従来、前記した電子部品の自動組入れシステム
に用いられる接着テープとしては、常温で粘着性
を有する通例の感圧性接着剤に熱溶融性樹脂を添
加してクリープ性を改良した感圧性接着剤からな
る層を支持テープに設けたものが知られていた
(特公昭56−13040号公報)。これは、常温で粘着
性を有する通例の感圧性接着剤のみからなるタイ
プの粘着テープではその感圧性接着剤層の大きい
クリープ性の故に電子部品連を定位置に維持する
ことが難しく、電子部品連の位置ズレで感知不能
となつて電子計算機が制御できなくなり自動組入
れシステムがストツプするという問題点の克服を
目的としたものである。
発明が解決しようとする問題点
しかしながら、前記した従来の接着テープにあ
つては、その感圧性接着剤層が通例の感圧性接着
剤に所定の融点を有する熱溶融性樹脂を添加する
ことにより接着性と耐熱性のバランスをとつたも
のであるため、満足できる特性を有するものを得
にくいという問題点があつた。すなわち、活性温
度が100℃以下となる組成とした場合には、クリ
ープ性が満足に改良されないでそれまでの感圧性
接着剤と同様の電子部品連の位置ズレ、自動組入
れシステムのストツプの問題が発生し、この点を
改良して満足できる程度の耐クリープ性を示す組
成とした場合には、その活性に要する温度が100
℃を超えることとなり、従つて熱収縮等の点より
定間隔連設の実現に支持テープに相当な耐熱性が
要求されるという問題、あるいはリード線に貼り
付けたのちにも溶融状態が必要以上に続き、電子
部品の位置ズレを防止するために冷却工程を必要
とするポツトライフ的な問題、更には低温脆化が
大きくて0℃以下などの低温保存をした場合に小
さい衝撃力で電子部品の剥れないし位置ズレ等が
生じる問題、従つて低温保存ができないという問
題などが発生することとなる。
問題点を解決するための手段
本発明者らは上記の問題点を克服し、約40〜80
℃の比較的低温で活性化することができると共に
リード線貼着後に冷却のための特別な工程を要さ
ず、しかも低温保存が可能な電子部品連設用の接
着テープを開発するために鋭意研究を重ねた結
果、ベースポリマとしてガラス転移点の高い重合
体を側鎖に有するアクリ系の特殊なグラフトポリ
マを用いることによりその目的を達成しうること
を見出し、本発明をなすに至つた。
すなわち、本発明は、炭素数が1〜12のアルキ
ル基を有するアクリル酸系エステル50〜99重量部
と、不飽和カルボン酸1〜15重量部と、エチレン
基含有共重合性モノマ0〜49重量部との反応生成
物からなる室温粘着性の共重合体を主鎖とし、ガ
ラス転移点が70〜150℃の重合体を側鎖とするグ
ラフトポリマ100重量部に融点が70〜200℃の熱溶
融性樹脂を50〜200重量部配合してなる熱時感圧
性接着剤の層を支持テープに設けてなり、リード
線を介して電子部品をスダレ状の配列となるよう
に連設保持するための接着テープを提供するもの
である。
本発明において用いられる熱時感圧性接着剤は
アクリル系グラフトポリマに熱溶融性樹脂を配合
したものである。これにより、加熱接着処理前の
室温において電子部品のリード線の仮止めが可能
で、しかも比較的低温の加熱処理により短時間で
活性化されて充分なぬれ性等の接着性を示すと共
に、固化後の接着強度に優れ、かつ耐クリープ性
に優れるものとすることができる。
本発明において前記アクリル系グラフトポリマ
は、炭素数が1〜12のアルキル基を有するアクリ
ル酸系エステルと不飽和カルボン酸との共重合体
又は、これらのほかに第3成分としてエチレン基
含有共重合性モノマを含む共重合体からなる室温
粘着性の共重合体を主鎖とし、ガラス転移点が70
〜150℃の重合体を側鎖とするものである。側鎖
成分としての重合体のガラス転移点が70℃未満で
あると耐熱性が充分に改善されないし、150℃を
超えるとぬれ性等の接着性が低下して好ましくな
い。
該グラフトポリマの調製は、例えば溶液重合方
式、乳化重合方式、塊状重合方式、懸濁重合方式
などにより行うことができる。
本発明においては該グラフトポリマを調製する
ための共重合体として、アクリル酸系エステル50
〜99重量部と、不飽和カルボン酸1〜15重量部
と、エチレン基含有共重合性モノマ0〜49重量部
との反応生成物からなるものが用いられる。アク
リル酸系エステルの使用量が50重量部未満である
と、得られる熱時感圧性接着剤が満足できる接着
性を有しなし、不飽和カルボン酸の使用量が1重
量部未満であると得られる熱時感圧性接着剤が接
着強度に劣り、15重量部を超えると接着性に劣
る。なお、接着性と接着強度とのバランスを調整
するために必要に応じ主鎖中に組み込まれるエチ
レン基含有共重合性モノマの使用量が49重量部を
超えると、得られる熱時感圧性接着剤の接着性が
低下する。
なお、グラフトポリマとしては、前記した共重
合体100重量部と所定のガラス転移点を有する重
合体3〜30重量部との反応生成物からなるものが
好ましく用いられる。該重合体の使用量が3重量
部未満であると得られる熱時感圧性接着剤が充分
な耐熱性を有さず、30重量部を超えると接着性が
低下する場合がある。
本発明の熱時感圧性接着剤における熱溶融性樹
脂の配合量としては、グラフトポリマ100重量部
あたり50〜200重量部が適当である。その配合量
が50重量部未満であると得られた接着剤が加熱溶
融から再固化までに長時間を要するもとなつた
り、その接着力が弱くなつたりし、200重量部を
超えると得られる接着剤が脆くなつたり、被着体
に対するぬれ性が劣つたりして好ましくない。本
発明においては融点が70〜200℃の熱溶融性樹脂
が用いられる。その融点が70℃未満のものでは得
られる接着剤が固化後の接着力に劣り、200℃を
超えるものでは得られる接着剤の活性化に多くの
熱量を要することとなつて好ましくない。
上記した共重合体を調製するための炭素数が1
〜12のアルキル基を有するアクリル酸系エステル
の好ましいものの例としては、アクリル酸エチ
ル、アクリル酸ブチル、アクリル酸2―エチルヘ
キシル、アクリル酸イソオクチル、アクリル酸イ
ソノニル、メタクリル酸ブチル、メタクリル酸2
―エチルヘキシル、メタクリル酸イソオクチル、
メタクリル酸イソノニルなどのアクリル酸ないし
メタクリル酸のエステルをあげることができる。
また、不飽和カルボン酸の好ましいものの例と
しては、アクリル酸、メタクリル酸、イタコン酸
などで代表されるα,β―不飽和カルボン酸など
をあげることができる。
一方、必要に応じ用いられるエチレン基含有共
重合性モノマの好ましいものの例としては、2―
ヒドロキシエチル基、2―ヒドロキシプロピル
基、2―メトキシエチル基、グリシジル基を有す
るアクリル酸ないしメタクリル酸のエステル、酢
酸ビニル、プロピオン酸ビニル、アクリロニトリ
ル、スチレン、ビニルトルエンなどで代表される
エチレン性二重結合を一つ有する化合物をあげる
ことができる。
他方、グラフトポリマにおける側鎖成分として
の重合体の好ましいものの例としては、メタクリ
ル酸メチル、スチレン、ビニルトルエン、アクリ
ル酸、メタクリル酸などからなるものをあげるこ
とができる。
好ましく用いうる熱溶融性樹脂の例としは、フ
エノール系樹脂、キシレン系樹脂、ポリテルペン
系樹脂、クマロンインデン系樹脂、エポキシ系樹
脂、ロジン系樹脂などをあげることができる。
本発明の接着テープは、上記した熱時感圧性接
着剤の層を支持テープに設けたものである。その
支持テープとしては例えばクレープ紙、クラフト
紙のような紙材、プラスチツクのフイルムないし
シート、布、金属箔などが一般に用いられる。熱
時感圧性接着剤の層厚としては30〜200μmが適当
である。
なお、いずれの構成成分ないし構成条件も上記
に限定するものでない。また、いずれの構成成分
も1種のみを用いてもよいし、2種以上を併用し
てもよい。
本発明の接着テープの適用は、限定するもので
はないが例えば次のようにして行うことができ
る。すなわち、電部品のリード線の端末部分を接
着テープの熱時感圧性接着剤層に仮止めする方式
で、個々の電子部品をスダレ状の配列状態となる
ように等間隔に連設して位置決めしたのち、これ
に例えば坪量100〜300g/m2のクラフト紙、ボー
ル紙の如く自己支持性を有するテープ状基材をリ
ード線を介して該熱時感圧性接着剤層に貼り合わ
せ、40〜80℃で0.1〜1秒間加熱処理することに
より行うことができる。このようにして、回路基
板等の作製工程に電子部品を自動的に供給するた
めの自動組入れシステムに好適な個々の電子部品
が接着テープによりスダレ状の配列で連設され、
かつ強固に接着保持されたものが得られる。
発明の効果
本発明によれば特殊な熱時感圧性接着剤を用い
たので、加熱接着処理前の室温においてリード線
を介しての電子部品の仮止めが可能であり、比較
的低温の短時間加熱処理で電子部品を強固に連設
固定することができると共に、耐クリープ性に優
れることに基づいて電子部品の連設状態の維持性
ないし電子部品の定位置保持性に優れる接着テー
プとすることができる。また、本発明の接着テー
プは低温下における耐脆性にも優れ、形成された
電子部品連設体の低温保存も可能であるなどの利
点も有している。
実施例
参考例 1
開始剤として4,4′―アゾビス―4―シアノバ
レリアン酸を2部(重量部、以下同様)、連鎖移
動剤としてヨード酢酸を5部含む酢酸エチル中で
スチレン100部を70℃で24時間反応させ、ガラス
転移点(Tg)が100℃の末端カルボキシル化ポリ
スチレン(重量平均分子量約10000)を得た。
次に、得られた末端カルボキシル化ポリスチレ
ン100部とメタクリル酸グリシジル4部とをキシ
レン中でヒドロキノンの存在下、トリーn―ブチ
ルアミンを触媒として反応させ、ポリスチリルメ
タクリレートを得た。
参考例 2
アクリル酸ブチル80部、アクリル酸エチル16部
及びメタクリル酸4部を酢酸エチル中で2,2′―
アゾビスイソブチロニトリル0.1部を開始剤とし
て60℃で7時間反応させ、重量平均分子量約
800000のポリマの溶液を得た。
実施例 1
アクリル酸2―エチルヘキシル70部、酢酸ビニ
ル20部、アクリル酸10部及び参考例1のポリスチ
リルメタクリレート5部をアセトン中で2,2′―
アゾビスイソブチロニトリル0.2部を開始剤とし
て55℃で10時間反応させて得た、重量平均分子量
約700000のグラフトポリマ(A)の溶液に、このポリ
マ100部あたり100部のテルペン変性フエノール樹
脂(融点100℃)と0.5部のポリイソシアネートを
添加して混合し、これを坪量80g/m2のクレープ
紙上に乾燥後の厚さが40μmとなるように塗布し、
80℃で5分間乾燥処理して本発明の接着テープを
得た。
実施例 2
参考例2の溶液にそのポリマ100部あたり過酸
化ベンゾイル0.5部を加え、これにメタクリル酸
メチル(ホモポリマのTg、105℃)20部を70℃で
3時間かけて滴下したのち、さらに2時間、75℃
で反応させて得た重量平均分子量約800000のグラ
フトポリマ(B)の溶液に、このポリマ100部あたり
120部のフエノール変性キシレン樹脂(融点80℃)
と1部のポリイソシアネートを添加して混合し、
これを実施例1と同様に適用処理して本発明の接
着テープを得た。
比較例 1
参考例2の溶液にその固形分100部あたり120部
のフエノール変性キシレン樹脂(融点80℃)と1
部のポリイソシアネートを添加して混合し、これ
を接着剤成分として用いたほかは実施例1に準じ
て接着テープを得た。
比較例 2
参考例2の溶液にその固形分100部あたり1部
のポリイソシアネートを添加して混合し、これを
接着剤成分として用いたほかは実施例1に準じて
接着テープを得た。
評価試験
実施例及び比較例で得た接着テープの接着剤面
に、U字形に折り曲げられた直径0.5mmのリード
線を有する電子部品を5mmの間隔をあけてかつ、
リード線の両端が平行に配列する状態となるよう
に20℃、65%R.H.条件下にそのリード線の端部
の長さ15mmにわたる部分を仮止めしたのち、接着
面の上にリード線を介して坪量220g/m2のボー
ル紙テープ(幅15mm)を重ね合わせて80℃、20
Kg/cm2×0.3秒間の条件で加熱圧着して試験片を
作製し、下記の試験に供した。
保持性能
60℃の温度下でリード線の折り曲げ部に50g、
100g又は200gの荷重をかけて2時間放置したの
ちの位置ズレ距離を調べた。
結果を第1表に示した。
Industrial Application Field The present invention has a layer of a novel pressure-sensitive adhesive when heated, which is made of an acrylic graft polymer mixed with a hot-melt resin. This invention relates to an adhesive tape for holding an array in series. Conventional technology Electronic components with lead wires are held in a sag-like arrangement by sandwiching the lead wires between adhesive tape and non-adhesive tape, and the electronic components are automatically supplied to the manufacturing process of circuit boards, etc. A system for automatically assembling electronic parts is known
Publication No. 12368). In other words, under the control of a computer, the terminal ends of the lead wires of the electronic components arranged in a sagging pattern are cut to unravel the connected state, and the unraveled electronic components are automatically incorporated into the manufacturing process one by one to form circuit boards, etc. It is known how to assemble. In this automatic assembly system, it is required that the electronic components be attached to the adhesive tape with high precision, evenly spaced, and parallel to each other. Conventionally, adhesive tapes used in the above-mentioned automatic assembly systems for electronic components are made of pressure-sensitive adhesives that have improved creep properties by adding a heat-melting resin to ordinary pressure-sensitive adhesives that are sticky at room temperature. It was known that the layer was provided on a support tape (Japanese Patent Publication No. 13040/1983). This is because it is difficult to keep electronic parts in place with adhesive tapes made only of ordinary pressure-sensitive adhesives that are sticky at room temperature due to the large creep property of the pressure-sensitive adhesive layer. This is aimed at overcoming the problem that the automatic installation system stops because the computer cannot control the electronic computer due to positional deviation of the link. Problems to be Solved by the Invention However, in the conventional adhesive tape described above, the pressure-sensitive adhesive layer is bonded by adding a heat-melting resin having a predetermined melting point to a common pressure-sensitive adhesive. The problem was that it was difficult to obtain products with satisfactory properties because they had to strike a balance between strength and heat resistance. In other words, if the composition has an activation temperature of 100°C or less, the creep property will not be satisfactorily improved, and problems such as misalignment of electronic components and stoppage of automatic assembly systems, similar to those of previous pressure-sensitive adhesives, will occur. If this point is improved to create a composition that exhibits satisfactory creep resistance, the temperature required for its activation will be 100°C.
℃, and therefore, due to heat shrinkage, etc., the supporting tape needs to have considerable heat resistance to realize continuous connection at regular intervals, or the molten state may exceed the necessary level even after it is attached to the lead wire. Following this, there are pot-life problems that require a cooling process to prevent electronic components from shifting, and furthermore, low-temperature embrittlement is significant, and electronic components can be damaged by small impact forces when stored at temperatures below 0°C. This results in problems such as not being able to peel off, misalignment, etc., and therefore not being able to be stored at low temperatures. Means for Solving the Problems The present inventors have overcome the above problems and have
We worked hard to develop an adhesive tape for connecting electronic components that can be activated at a relatively low temperature of ℃, does not require a special process for cooling after attaching lead wires, and can be stored at low temperatures. As a result of repeated research, it was discovered that the purpose could be achieved by using a special acrylic graft polymer having a polymer with a high glass transition point in the side chain as a base polymer, and the present invention was completed. That is, the present invention comprises 50 to 99 parts by weight of an acrylic ester having an alkyl group having 1 to 12 carbon atoms, 1 to 15 parts by weight of an unsaturated carboxylic acid, and 0 to 49 parts by weight of an ethylene group-containing copolymerizable monomer. 100 parts by weight of a graft polymer whose main chain is a room-temperature sticky copolymer made from a reaction product of a reaction product with a glass transition point of 70 to 150°C, and a side chain of a polymer with a glass transition point of 70 to 150°C, is heated to a temperature of 70 to 200°C. A support tape is provided with a layer of heat-sensitive adhesive containing 50 to 200 parts by weight of a meltable resin, and is used to hold electronic components connected in a sagging arrangement via lead wires. adhesive tape. The heat-sensitive adhesive used in the present invention is a mixture of an acrylic graft polymer and a heat-melting resin. This makes it possible to temporarily fix lead wires of electronic components at room temperature before heat bonding, and is activated in a short time by heat treatment at a relatively low temperature, exhibiting sufficient adhesive properties such as wettability, and solidifying. It is possible to obtain excellent adhesive strength and creep resistance. In the present invention, the acrylic graft polymer is a copolymer of an acrylic ester having an alkyl group having 1 to 12 carbon atoms and an unsaturated carboxylic acid, or a copolymer containing an ethylene group as a third component. The main chain is a room-temperature adhesive copolymer made of a copolymer containing a polyvalent monomer, and the glass transition point is 70.
The side chain is a polymer with a temperature of ~150°C. If the glass transition point of the polymer as a side chain component is less than 70°C, the heat resistance will not be sufficiently improved, and if it exceeds 150°C, adhesive properties such as wettability will deteriorate, which is undesirable. The graft polymer can be prepared by, for example, a solution polymerization method, an emulsion polymerization method, a bulk polymerization method, a suspension polymerization method, or the like. In the present invention, as a copolymer for preparing the graft polymer, acrylic acid ester 50
A reaction product of 99 parts by weight, 1 to 15 parts by weight of an unsaturated carboxylic acid, and 0 to 49 parts by weight of an ethylene group-containing copolymerizable monomer is used. If the amount of the acrylic acid ester used is less than 50 parts by weight, the resulting hot pressure-sensitive adhesive will not have satisfactory adhesive properties, and if the amount of the unsaturated carboxylic acid used is less than 1 part by weight, the resulting hot pressure-sensitive adhesive will not have satisfactory adhesive properties. The adhesive strength of the hot pressure sensitive adhesive used is poor, and if it exceeds 15 parts by weight, the adhesive property is poor. In addition, if the amount of the ethylene group-containing copolymerizable monomer, which is incorporated into the main chain as necessary to adjust the balance between adhesiveness and adhesive strength, exceeds 49 parts by weight, the resulting hot pressure-sensitive adhesive The adhesion of the product decreases. As the graft polymer, a reaction product of 100 parts by weight of the aforementioned copolymer and 3 to 30 parts by weight of a polymer having a predetermined glass transition point is preferably used. If the amount of the polymer used is less than 3 parts by weight, the resulting hot pressure-sensitive adhesive will not have sufficient heat resistance, and if it exceeds 30 parts by weight, the adhesive properties may decrease. The appropriate amount of the heat-melting resin in the hot pressure-sensitive adhesive of the present invention is 50 to 200 parts by weight per 100 parts by weight of the graft polymer. If the amount is less than 50 parts by weight, the resulting adhesive may take a long time to re-solidify from heating and melting, or its adhesive strength may become weak; if it exceeds 200 parts by weight, This is undesirable because the adhesive becomes brittle and has poor wettability to the adherend. In the present invention, a thermofusible resin having a melting point of 70 to 200°C is used. If the melting point is less than 70°C, the resulting adhesive will have poor adhesive strength after solidification, and if it exceeds 200°C, a large amount of heat will be required to activate the resulting adhesive, which is undesirable. The number of carbon atoms for preparing the above copolymer is 1.
Preferred examples of acrylic esters having ~12 alkyl groups include ethyl acrylate, butyl acrylate, 2-ethylhexyl acrylate, isooctyl acrylate, isononyl acrylate, butyl methacrylate, and 2-ethylhexyl acrylate.
-Ethylhexyl, isooctyl methacrylate,
Examples include esters of acrylic acid or methacrylic acid such as isononyl methacrylate. Preferred examples of unsaturated carboxylic acids include α,β-unsaturated carboxylic acids represented by acrylic acid, methacrylic acid, itaconic acid, and the like. On the other hand, preferred examples of the ethylene group-containing copolymerizable monomer used as necessary include 2-
Acrylic acid or methacrylic acid esters having a hydroxyethyl group, 2-hydroxypropyl group, 2-methoxyethyl group, or glycidyl group, ethylenic double esters represented by vinyl acetate, vinyl propionate, acrylonitrile, styrene, vinyltoluene, etc. Examples include compounds that have one bond. On the other hand, preferred examples of polymers as side chain components in the graft polymer include those consisting of methyl methacrylate, styrene, vinyltoluene, acrylic acid, methacrylic acid, and the like. Examples of thermomeltable resins that can be preferably used include phenol resins, xylene resins, polyterpene resins, coumaron indene resins, epoxy resins, and rosin resins. The adhesive tape of the present invention is one in which a support tape is provided with a layer of the above-mentioned heat-sensitive adhesive. As the supporting tape, for example, a paper material such as crepe paper or kraft paper, a plastic film or sheet, cloth, metal foil, etc. are generally used. The appropriate layer thickness of the pressure-sensitive adhesive when heated is 30 to 200 μm. Note that none of the constituent components or constituent conditions are limited to those described above. Further, each of the constituent components may be used alone or in combination of two or more. The adhesive tape of the present invention can be applied, for example, as follows, although it is not limited thereto. In other words, the terminals of the lead wires of the electronic components are temporarily fixed to the heat-sensitive adhesive layer of the adhesive tape, and the individual electronic components are aligned and positioned at equal intervals so that they are arranged in a sagging pattern. After that, a self-supporting tape-like base material such as kraft paper or cardboard with a basis weight of 100 to 300 g/m 2 is attached to the hot pressure-sensitive adhesive layer via lead wires, and the adhesive layer is heated for 40 minutes. This can be carried out by heat treatment at ~80°C for 0.1 to 1 second. In this way, individual electronic components suitable for an automatic assembly system for automatically supplying electronic components to the manufacturing process of circuit boards etc. are connected in a sagging arrangement using adhesive tape.
Moreover, a product that is firmly adhesively held can be obtained. Effects of the Invention According to the present invention, since a special heat-sensitive adhesive is used, it is possible to temporarily fix electronic components via lead wires at room temperature before heat bonding, and for a short time at a relatively low temperature. To provide an adhesive tape that can firmly connect and fix electronic components in a continuous manner by heat treatment, and has excellent creep resistance to maintain the continuous state of electronic components or hold electronic components in a fixed position. Can be done. Further, the adhesive tape of the present invention has advantages such as excellent brittleness resistance at low temperatures and the ability to store the formed electronic component assembly at low temperatures. Examples Reference Example 1 100 parts of styrene was added to 70 parts of styrene in ethyl acetate containing 2 parts (by weight, same hereinafter) of 4,4'-azobis-4-cyanovaleric acid as an initiator and 5 parts of iodoacetic acid as a chain transfer agent. The reaction was carried out at ℃ for 24 hours to obtain terminal carboxylated polystyrene (weight average molecular weight about 10,000) with a glass transition point (Tg) of 100℃. Next, 100 parts of the obtained terminally carboxylated polystyrene and 4 parts of glycidyl methacrylate were reacted in xylene in the presence of hydroquinone using tri-n-butylamine as a catalyst to obtain polystyryl methacrylate. Reference Example 2 80 parts of butyl acrylate, 16 parts of ethyl acrylate and 4 parts of methacrylic acid were mixed in ethyl acetate with 2,2'-
Using 0.1 part of azobisisobutyronitrile as an initiator, the reaction was carried out at 60°C for 7 hours, and the weight average molecular weight was approx.
A solution of 800,000 polymers was obtained. Example 1 70 parts of 2-ethylhexyl acrylate, 20 parts of vinyl acetate, 10 parts of acrylic acid, and 5 parts of the polystyryl methacrylate of Reference Example 1 were mixed with 2,2'- in acetone.
Add 100 parts of terpene-modified phenol resin per 100 parts of this polymer to a solution of graft polymer (A) with a weight average molecular weight of about 700,000, which was obtained by reacting at 55°C for 10 hours with 0.2 parts of azobisisobutyronitrile as an initiator. (melting point 100°C) and 0.5 part of polyisocyanate were added and mixed, and this was applied onto crepe paper with a basis weight of 80 g/m 2 so that the thickness after drying was 40 μm.
The adhesive tape of the present invention was obtained by drying at 80° C. for 5 minutes. Example 2 0.5 parts of benzoyl peroxide per 100 parts of the polymer was added to the solution of Reference Example 2, and 20 parts of methyl methacrylate (Tg of homopolymer, 105°C) was added dropwise at 70°C over 3 hours. 2 hours, 75℃
per 100 parts of the graft polymer (B) with a weight average molecular weight of about 800,000 obtained by reacting with
120 parts of phenol-modified xylene resin (melting point 80°C)
and 1 part of polyisocyanate are added and mixed,
This was applied and treated in the same manner as in Example 1 to obtain an adhesive tape of the present invention. Comparative Example 1 The solution of Reference Example 2 was mixed with 120 parts of phenol-modified xylene resin (melting point 80°C) per 100 parts of its solid content.
An adhesive tape was obtained in the same manner as in Example 1, except that a portion of polyisocyanate was added and mixed, and this was used as an adhesive component. Comparative Example 2 An adhesive tape was obtained in accordance with Example 1, except that 1 part of polyisocyanate per 100 parts of the solid content was added to the solution of Reference Example 2 and mixed, and this was used as an adhesive component. Evaluation Test An electronic component having a lead wire with a diameter of 0.5 mm bent into a U shape was placed on the adhesive surface of the adhesive tape obtained in the Examples and Comparative Examples with an interval of 5 mm, and
Temporarily fasten the ends of the lead wires over a length of 15 mm under conditions of 20°C and 65% RH so that both ends of the lead wires are aligned in parallel, and then place the lead wires on the adhesive surface. Layer cardboard tapes (width 15 mm) with a basis weight of 220 g/ m2 and heat them at 80℃ for 20 minutes.
A test piece was prepared by heating and pressing under the conditions of Kg/cm 2 ×0.3 seconds, and was subjected to the following test. Retention performance 50g at the bent part of the lead wire at a temperature of 60℃,
After applying a load of 100g or 200g and leaving it for 2 hours, the displacement distance was examined. The results are shown in Table 1.
【表】
接着性能
0℃、20℃又は40℃の温度下においてリード線
の引き抜き(速度300mm/分)に要する力を調べ
た。
結果を第2表に示した。[Table] Adhesive Performance The force required to pull out the lead wire (at a speed of 300 mm/min) was investigated at temperatures of 0°C, 20°C, or 40°C. The results are shown in Table 2.
【表】
第1表及び第2表より、実施例としての本発明
の接着テープによれば、荷重が負荷された状態に
おいても電子部品の位置ズレが起こりにくく、強
固な力で電子部品ないしそのリード線が保持され
ていること、低温保存が可能なことがわかる。[Table] From Tables 1 and 2, it can be seen that according to the adhesive tape of the present invention as an example, electronic components are unlikely to be misaligned even when a load is applied, and strong force can be applied to electronic components or their It can be seen that the lead wires are retained and that low temperature storage is possible.
Claims (1)
ル酸系エステル50〜99重量部と、不飽和カルボン
酸1〜15重量部と、エチレン基含有共重合性モノ
マ0〜49重量部との反応生成物からなる室温粘着
性の共重合体を主鎖とし、ガラス転移点が70〜
150℃の重合体を側鎖とするグラフトポリマ100重
量部に融点が70〜200℃の熱溶融性樹脂を50〜200
重量部配合してなる熱時感圧性接着剤の層を支持
テープに設けてなり、リード線を介して電子部品
をスダレ状の配列となるように連設保持するため
の接着テープ。 2 アクリル酸系エステルがアクリル酸又はメタ
クリル酸のエステルであり、不飽和カルボン酸が
α,β―不飽和カルボン酸である特許請求の範囲
第1項記載の接着テープ。 3 エチレン基含有共重合性モノマがエチレン性
二重結合を一つ有するものである特許請求の範囲
第1項記載の接着テープ。 4 グラフトポリマが室温粘着性の共重合体100
重量部と前記ガラス転移点の重合体3〜30重量部
との反応生成物である特許請求の範囲第1項記載
の接着テープ。 5 熱溶融性樹脂がフエノール系樹脂、キシレン
系樹脂、ポリテルペン系樹脂、クマロンインデン
系樹脂、エポキシ系樹脂又は/及びロジン系樹脂
である特許請求の範囲第1項記載の接着テープ。[Scope of Claims] 1. 50 to 99 parts by weight of an acrylic ester having an alkyl group having 1 to 12 carbon atoms, 1 to 15 parts by weight of an unsaturated carboxylic acid, and 0 to 49 parts by weight of an ethylene group-containing copolymerizable monomer The main chain is a room-temperature sticky copolymer consisting of a reaction product with parts by weight, and the glass transition point is 70~
Add 50 to 200 parts by weight of a thermofusible resin with a melting point of 70 to 200°C to 100 parts by weight of a graft polymer whose side chain is a 150°C polymer.
An adhesive tape for holding electronic components connected in a sag-like arrangement via lead wires, the support tape being provided with a layer of a heat-sensitive adhesive in a proportion by weight of the adhesive. 2. The adhesive tape according to claim 1, wherein the acrylic acid ester is an ester of acrylic acid or methacrylic acid, and the unsaturated carboxylic acid is an α,β-unsaturated carboxylic acid. 3. The adhesive tape according to claim 1, wherein the ethylene group-containing copolymerizable monomer has one ethylenic double bond. 4 Copolymer 100 whose graft polymer is adhesive at room temperature
2. The adhesive tape according to claim 1, which is a reaction product of 3 to 30 parts by weight of said glass transition point polymer. 5. The adhesive tape according to claim 1, wherein the heat-melting resin is a phenol resin, a xylene resin, a polyterpene resin, a coumaron indene resin, an epoxy resin, or/and a rosin resin.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP60296604A JPS62149782A (en) | 1985-12-24 | 1985-12-24 | Adhesive tape for joining electronic component |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP60296604A JPS62149782A (en) | 1985-12-24 | 1985-12-24 | Adhesive tape for joining electronic component |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS62149782A JPS62149782A (en) | 1987-07-03 |
| JPH0146548B2 true JPH0146548B2 (en) | 1989-10-09 |
Family
ID=17835700
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP60296604A Granted JPS62149782A (en) | 1985-12-24 | 1985-12-24 | Adhesive tape for joining electronic component |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS62149782A (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH02219883A (en) * | 1989-02-22 | 1990-09-03 | Nitto Denko Corp | Thermosetting repeelable pressure-sensitive adhesive, pressure sensitive tape using it and holding structure for electronic component |
| JP2905990B2 (en) * | 1989-07-31 | 1999-06-14 | 藤森工業株式会社 | Manufacturing method of adhesive tape for continuous formation of electronic parts |
| JP2002226793A (en) * | 2001-01-31 | 2002-08-14 | Nitto Denko Corp | Adhesive tape for connecting electronic components |
-
1985
- 1985-12-24 JP JP60296604A patent/JPS62149782A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS62149782A (en) | 1987-07-03 |
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| Date | Code | Title | Description |
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| EXPY | Cancellation because of completion of term |