JP4073041B2 - ミクロ範囲の接着用熱硬化性一成分lva(低粘度接着型)接着剤系 - Google Patents
ミクロ範囲の接着用熱硬化性一成分lva(低粘度接着型)接着剤系 Download PDFInfo
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Description
ミクロ接着に対して一般に樹脂及び硬化成分から成る接着剤系が公知である。これらの二成分接着剤系ではμm範囲の接着に必要とされる僅少量に問題がある。特に塗布直前の個々の成分の精確な配量、混合及び均質化に際して問題がある。またそれら接着剤系は一般に粘度が高過ぎ、従ってミクロ配量用の接着剤、いわゆるLVA(低粘度接着型)接着剤を塗布できるような稀溶液性には比較的高温(約70℃)で初めてなることは欠点である。更に公知の二成分系は薄層又は小滴で不均質性であるため不活性ガス又は窒素雰囲気でも不完全にしか硬化しないという欠点を有する。これら全ての要因により産業上の製造に要求される再現可能な品質で、μm及びサブμm範囲(=1μm以下)の結合強度及び寸法公差に関して工業的に使用できる接合を実現することは従来不可能であった。
従ってエレクトロニクス及びオプトエレクトロニクス分野の低コスト・システムの合理的で自動化されかつ安全で経済的に有利な接合技術を可能にする接着剤系が必要となる。特にμm範囲及びサブμm範囲の接着に極めて薄い層又は小滴の形で確実に配量し、硬化することができる接着剤系が必要となる。その際上記の寸法は硬化後も維持されなければならない。
従って本発明の課題は僅少量でも不均質性を示さず、μm範囲の配量に適した接着剤系を提供することにある。更に本発明の課題は薄層の形で完全に硬化する接着剤系を提供することにある。それにより接着剤による接合の信頼度及び強度が高められ、接着剤による接合後の不所望のガスの発生を低減できるようにする。更に本発明による接着剤系は公知の系に比べて低粘度でかつ良好な展延特性を示すものでなければならない。最後に本発明の接着剤系の耐久性はμm及びそれ以下の範囲の寸法公差で個々の部材を継ぎ合わすことを可能にすべきである。
この課題は本発明による接着剤系により解決される。本発明の対象は以下の組成
を含む熱硬化性の一成分系接着剤系である。
更にこのような接着剤系をμm及びサブμm範囲の寸法公差での接着に使用することが本発明の対象である。他の有利な実施態様は明細書の記載並びに実施例及び従属請求項から明らかとする。
本発明において使用する“エポキシ注型用樹脂”は、注型により適当な形に仕上げることのできるような低粘度の熱硬化性樹脂系及び反応樹脂を意味し、それらは熱的に、即ち適切な付加物(開始剤、促進剤、他の成分)の存在下に熱上昇により硬化可能である。このエポキシ注型用樹脂は本発明の配合物中に60〜98重量%の量で、有利には75〜95重量%、主として80〜95重量%及び特に有利には85〜93重量%の範囲で含まれている。
“エポキシ樹脂”としては、チバ・ガイギー(Ciba Geigy)社製の樹脂CY177(3,4−エポキシシクロヘキシルメチル−アジピン酸塩)を使用する。
“アルコール又は糖類”としては本発明では1〜15個のヒドロキシル基を有するアルコール又は糖類が使用される。有利には1〜5個のヒドロキシル基を有するアルコールが使用される。その際アルコール又は糖類の基本骨格は任意に変えることができ、脂肪族、環状又は二環状であっても、単結合のみ又は多重結合から成っていても、また芳香族系であってもよい。とりわけヘキスト(Hoechst)社のTCDアルコールDM、即ち3(4),8(9)−ビス(ヒドロキシメチル)トリシクロ[5.2.1.02.6]デカンを使用すると有利である。この有利には多価のアルコールは接着剤配合物中に2〜30重量%の分量で含まれている。有利にはこのアルコールは2.5〜20重量%の分量、特に有利には4.5〜12重量%の分量で含まれている。
熱開始剤としては従来の全ての陽イオンメカニズムで硬化する例えばオニウム塩のような開始剤を使用することができる。この場合アルドリッヒ(Aldrich)社のS−ベンジルチオラニウムヘキサフルオロアンチモネートが優先的に使用された。
接着促進剤としてはヒュルス(Huels)社のA187、即ち3−グリシジルオキシプロピルトリメトキシシランが使用される。
展延補助剤としてはモンサント(Monsanto)社のモダフロウ(Modaflow、商品名)を、また流れ調整剤又はチキソトロピー剤としては例えば市販されているデグッサ(Degussa)社のアエロシル(Aerosil、商品名)タイプを使用することができる。
既に記載した成分の他に本発明による接着剤系には更にそれ自体公知の添加物及び付加物を含むこともできる。それによりこの接着剤系は特に色又は透明度のような、また難燃性又は耐熱性などの付加特性を有することもできる。従ってこの意味での添加物は例えば色素、顔料、流れ調整剤、一般に安定剤、耐炎剤又は鉱物性又は他の充填剤であってもよい。その際添加物により一定の特性、例えば色素を介しての選択的吸収度又は透明度を達成することは常にほぼ可能である。
この接着剤系の製造は比較可能系と同じようにして行われる。エポキシ樹脂、多価アルコール、熱開始剤、接着促進剤及び場合によっては展延補助剤のような配合成分は場合によっては高めた温度下でもまた再除去可能の溶剤でも一様に相互に混合される。従ってこの接着剤系の製造には従来技術で行われている通常の方法に基づくことができる。
以下に本発明を実施例に基づき詳述する。表1は代表的な接着剤系の配合成分を示すものである。
表2には例として上記の配合物の選択された材料特性がまとめられている。
表3は配合物の貯蔵可能性の試験データを示している。観察期間は2ヶ月とし、その際冷蔵庫で貯蔵(5−8℃)した際例えば熱開始剤が晶質するようないかなる非融和もしくは分解を生じなかった。
本発明による接着剤系でμm及びサブμm範囲のエレクトロニクス及びオプトエレクトロニクス・コンポーネントの自動化された確実なミクロ接着が可能となる。本発明による一成分エポキシ注型用樹脂は直ちに硬化せず、従って個々の部材の継合わせは最終的に固着されるまで可能である。エポキシ樹脂成分並びに全ての接着剤系はミクロ接着の際に使用されるのに十分な低粘度である。最終的にアルコール又は糖類、特に多価アルコールで接着剤系の滴下特性、湿潤特性及び流れ特性並びに接着剤接合の機械的特性を調整することができる。
この接着剤系は問題なくミクロ量で配量することができ、滴下、湿潤及び展延挙動に関して更に展延補助剤の添加により最適化することができる。熱負荷により、即ち局部的加熱又は接着すべき部分の加熱によりこの接着剤系は迅速に均質な接着結合物に網状化する。
冒頭に記載したミクロ接着技術に関する公知の二成分系の接着配合物の欠点はこうして克服される。特に配量可能性及び配量精度が改善され、また不完全な混合及び混合誤差は回避され、粘度は低下する。
本発明は少なくとも注型用樹脂、特にエポキシ注型用樹脂及び多価アルコールから成る一成分接着剤系に関する。この低粘度の接着剤系はミクロ配量可能であり、貯蔵安定、完全硬化性であり、寸法公差がμm及びサブμm範囲の用途に適している。
Claims (3)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19629082A DE19629082A1 (de) | 1996-07-18 | 1996-07-18 | Thermisch härtbares einkomponentiges Low viskosity Adhesive-Klebstoffsystem für Verklebungen im Mikrobereich |
DE19629082.1 | 1996-07-18 | ||
PCT/DE1997/001505 WO1998003606A1 (de) | 1996-07-18 | 1997-07-17 | Thermish härtbares einkomponentiges lva(=low viskosity adhesive)-klebstoffsystem für verklebungen im mikrobereich |
Publications (2)
Publication Number | Publication Date |
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JP2000514859A JP2000514859A (ja) | 2000-11-07 |
JP4073041B2 true JP4073041B2 (ja) | 2008-04-09 |
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ID=7800230
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Application Number | Title | Priority Date | Filing Date |
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JP50645298A Expired - Fee Related JP4073041B2 (ja) | 1996-07-18 | 1997-07-17 | ミクロ範囲の接着用熱硬化性一成分lva(低粘度接着型)接着剤系 |
Country Status (8)
Country | Link |
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US (1) | US6207732B1 (ja) |
EP (1) | EP0912649B1 (ja) |
JP (1) | JP4073041B2 (ja) |
CN (1) | CN1121468C (ja) |
DE (2) | DE19629082A1 (ja) |
NO (1) | NO990222L (ja) |
TW (1) | TW509716B (ja) |
WO (1) | WO1998003606A1 (ja) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE19804595A1 (de) * | 1998-02-05 | 1999-08-12 | Siemens Ag | Thermisch härtbare Ein-Komponenten-Underfill-Masse |
US20030138434A1 (en) * | 2001-08-13 | 2003-07-24 | Campbell Robert L. | Agents for enhancing the immune response |
DE102005040126A1 (de) * | 2005-08-25 | 2007-03-01 | Altana Electrical Insulation Gmbh | Überzugsmasse |
DE102005056393A1 (de) * | 2005-11-24 | 2007-05-31 | Grünenthal GmbH | Multicyclische Verbindungen in druckempfindlichen Klebstoffen |
TWI666280B (zh) * | 2012-08-03 | 2019-07-21 | 南韓商Lg化學股份有限公司 | 黏合膜與使用彼之有機電子裝置的包封產物 |
CN102898785B (zh) * | 2012-09-05 | 2014-10-22 | 烟台德邦科技有限公司 | 一种用于智能卡的包封胶及其制备方法 |
US20160251762A1 (en) * | 2013-08-29 | 2016-09-01 | Cmi Uvk Gmbh | Method of treating a pickling solution for a pickling process |
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JPS55118429A (en) * | 1979-03-05 | 1980-09-11 | Mitsubishi Petrochem Co Ltd | Preparation of tricyclodecanedimethylol |
US4480059A (en) * | 1982-08-26 | 1984-10-30 | General Electric Company | Epoxy adhesives for poly(butylene terephthalate) |
AU595593B2 (en) * | 1986-05-07 | 1990-04-05 | Minnesota Mining And Manufacturing Company | Epoxy resin composition |
JP2719616B2 (ja) * | 1989-11-30 | 1998-02-25 | 日本電信電話株式会社 | 光硬化型精密接着剤 |
DE59208790D1 (de) * | 1991-06-19 | 1997-09-18 | Ciba Geigy Ag | Neue Harzsysteme mit niedrigeren Formtemperaturen |
US5494943A (en) * | 1993-06-16 | 1996-02-27 | Minnesota Mining And Manufacturing Company | Stabilized cationically-curable compositions |
-
1996
- 1996-07-18 DE DE19629082A patent/DE19629082A1/de not_active Ceased
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1997
- 1997-07-17 TW TW086110140A patent/TW509716B/zh active
- 1997-07-17 DE DE59711142T patent/DE59711142D1/de not_active Expired - Fee Related
- 1997-07-17 CN CN97197995A patent/CN1121468C/zh not_active Expired - Fee Related
- 1997-07-17 EP EP97935433A patent/EP0912649B1/de not_active Expired - Lifetime
- 1997-07-17 WO PCT/DE1997/001505 patent/WO1998003606A1/de active IP Right Grant
- 1997-07-17 JP JP50645298A patent/JP4073041B2/ja not_active Expired - Fee Related
- 1997-07-17 US US09/230,075 patent/US6207732B1/en not_active Expired - Fee Related
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1999
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Also Published As
Publication number | Publication date |
---|---|
WO1998003606A1 (de) | 1998-01-29 |
CN1230974A (zh) | 1999-10-06 |
DE19629082A1 (de) | 1998-01-22 |
EP0912649B1 (de) | 2003-12-17 |
NO990222D0 (no) | 1999-01-18 |
NO990222L (no) | 1999-03-15 |
EP0912649A1 (de) | 1999-05-06 |
DE59711142D1 (de) | 2004-01-29 |
TW509716B (en) | 2002-11-11 |
JP2000514859A (ja) | 2000-11-07 |
US6207732B1 (en) | 2001-03-27 |
CN1121468C (zh) | 2003-09-17 |
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