CN105637001B - 光湿气固化型树脂组合物、电子部件用粘接剂、以及显示元件用粘接剂 - Google Patents
光湿气固化型树脂组合物、电子部件用粘接剂、以及显示元件用粘接剂 Download PDFInfo
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- CN105637001B CN105637001B CN201480056635.1A CN201480056635A CN105637001B CN 105637001 B CN105637001 B CN 105637001B CN 201480056635 A CN201480056635 A CN 201480056635A CN 105637001 B CN105637001 B CN 105637001B
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Classifications
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JP5989902B2 (ja) * | 2014-03-26 | 2016-09-07 | 積水化学工業株式会社 | 光湿気硬化型樹脂組成物、電子部品用接着剤、及び、表示素子用接着剤 |
CN109679031A (zh) * | 2014-05-13 | 2019-04-26 | 积水化学工业株式会社 | 光湿固化型树脂组合物、电子部件用粘接剂及显示元件用粘接剂 |
JP6039080B2 (ja) * | 2014-05-30 | 2016-12-07 | 積水化学工業株式会社 | 狭額縁設計表示素子用接着剤 |
JP6023359B2 (ja) * | 2014-11-13 | 2016-11-09 | 積水化学工業株式会社 | 硬化体、電子部品、及び、表示素子 |
CN107074999B (zh) * | 2014-12-26 | 2019-02-01 | 思美定株式会社 | 光固化性组合物 |
JP6703409B2 (ja) * | 2015-02-10 | 2020-06-03 | 積水化学工業株式会社 | 光湿気硬化型樹脂組成物及び熱伝導性接着剤 |
WO2016163353A1 (ja) * | 2015-04-09 | 2016-10-13 | 積水化学工業株式会社 | 光湿気硬化型樹脂組成物、電子部品用接着剤、及び、表示素子用接着剤 |
JP6697306B2 (ja) * | 2016-03-31 | 2020-05-20 | ハリマ化成株式会社 | 湿気硬化併用光硬化型組成物、コンフォーマルコーティング剤及び硬化物 |
EP3549964A4 (en) * | 2016-11-30 | 2020-09-02 | Hitachi Chemical Company, Ltd. | TWO-PART CURABLE URETHANE COMPOSITION |
KR102598369B1 (ko) * | 2017-08-18 | 2023-11-03 | 세키스이가가쿠 고교가부시키가이샤 | 습기 경화형 수지 조성물, 전자 부품용 접착제, 및, 표시 소자용 접착제 |
KR102665572B1 (ko) | 2017-12-22 | 2024-05-14 | 세키스이가가쿠 고교가부시키가이샤 | 경화성 수지 조성물, 경화체, 전자 부품 및 조립 부품 |
JPWO2019203277A1 (ja) * | 2018-04-19 | 2021-03-18 | 積水化学工業株式会社 | 硬化性樹脂組成物、硬化体、電子部品及び組立部品 |
CN112673031B (zh) * | 2018-10-23 | 2024-04-05 | 积水化学工业株式会社 | 固化性树脂组合物和固化体 |
WO2020149379A1 (ja) * | 2019-01-18 | 2020-07-23 | 積水化学工業株式会社 | 光湿気硬化性樹脂組成物、及び硬化体 |
JP7453905B2 (ja) * | 2019-01-18 | 2024-03-21 | 積水化学工業株式会社 | 硬化性樹脂組成物、及び硬化体 |
JP7623808B2 (ja) * | 2019-10-07 | 2025-01-29 | 日東電工株式会社 | 光硬化性粘着剤組成物、両面粘着シートおよびその製造方法、ならびに光学デバイスおよびその製造方法 |
JP7563170B2 (ja) * | 2020-12-24 | 2024-10-08 | artience株式会社 | ポリオール主剤、ポリウレタン接着剤、及び積層体 |
CN114133530B (zh) * | 2021-12-30 | 2023-08-08 | 深圳市库泰克电子材料技术有限公司 | 带nco反应基团的聚氨酯丙烯酸酯及具有该树脂的uv湿气固化胶粘剂 |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001064543A (ja) * | 1999-08-27 | 2001-03-13 | Nippon Shokubai Co Ltd | 硬化型被覆材用樹脂組成物 |
WO2013016133A2 (en) * | 2011-07-22 | 2013-01-31 | H.B. Fuller Company | A one-component, dual-cure adhesive for use on electronics |
Family Cites Families (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5826022B2 (ja) * | 1976-12-21 | 1983-05-31 | 富士ゼロックス株式会社 | 電子写真用感光材料 |
JPH05295064A (ja) * | 1992-04-24 | 1993-11-09 | Dainippon Ink & Chem Inc | 湿気硬化型ポリウレタン組成物 |
JP3608720B2 (ja) * | 2000-04-14 | 2005-01-12 | 大日本インキ化学工業株式会社 | 揺変性湿気硬化型ウレタン組成物及びコーティング材、シーリング材、接着剤 |
JP3637565B2 (ja) * | 2001-02-20 | 2005-04-13 | 大日本インキ化学工業株式会社 | 揺変性湿気硬化型ウレタン組成物 |
JP2004018621A (ja) * | 2002-06-14 | 2004-01-22 | Nippon Shokubai Co Ltd | ラジカル硬化性ウレタン樹脂組成物 |
JP2005187615A (ja) * | 2003-12-25 | 2005-07-14 | Yunimatekku Kk | 紫外線硬化型アクリル系組成物 |
JP5105134B2 (ja) * | 2005-05-13 | 2012-12-19 | 株式会社スリーボンド | 硬化性組成物及びそれを用いた放熱部材の形成方法 |
CN101228248B (zh) * | 2005-07-22 | 2012-05-09 | 株式会社普利司通 | 密封用材料、其制造方法以及使用密封用材料的密封垫 |
JP5009690B2 (ja) * | 2006-06-15 | 2012-08-22 | 日東電工株式会社 | 偏光板、画像表示装置および偏光板の製造方法 |
JP4936111B2 (ja) * | 2006-07-27 | 2012-05-23 | Dic株式会社 | 接着剤用硬化型樹脂組成物 |
JP5228370B2 (ja) | 2007-04-27 | 2013-07-03 | 東亞合成株式会社 | 一液湿気硬化型ウレタン系ホットメルト接着剤組成物及びその使用方法 |
JP5624280B2 (ja) * | 2009-04-14 | 2014-11-12 | 株式会社カネカ | フラットパネルディスプレイ表示モジュール/透明カバーボード間充填用硬化性組成物およびそれを塗布硬化させて得られるフラットパネルディスプレイを搭載した電気・電子機器 |
JP5407646B2 (ja) * | 2009-08-04 | 2014-02-05 | 東亞合成株式会社 | 電極被覆用光硬化型組成物 |
CN102816551A (zh) * | 2012-05-23 | 2012-12-12 | 烟台信友电子有限公司 | 一种uv-湿气双固化液态光学透明胶及其制备方法 |
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Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001064543A (ja) * | 1999-08-27 | 2001-03-13 | Nippon Shokubai Co Ltd | 硬化型被覆材用樹脂組成物 |
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