JP7217565B1 - 樹脂組成物、接着剤、封止材、硬化物、半導体装置及び電子部品 - Google Patents
樹脂組成物、接着剤、封止材、硬化物、半導体装置及び電子部品 Download PDFInfo
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- JP7217565B1 JP7217565B1 JP2022173402A JP2022173402A JP7217565B1 JP 7217565 B1 JP7217565 B1 JP 7217565B1 JP 2022173402 A JP2022173402 A JP 2022173402A JP 2022173402 A JP2022173402 A JP 2022173402A JP 7217565 B1 JP7217565 B1 JP 7217565B1
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Images
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/02—Polycondensates containing more than one epoxy group per molecule
- C08G59/04—Polycondensates containing more than one epoxy group per molecule of polyhydroxy compounds with epihalohydrins or precursors thereof
- C08G59/06—Polycondensates containing more than one epoxy group per molecule of polyhydroxy compounds with epihalohydrins or precursors thereof of polyhydric phenols
- C08G59/066—Polycondensates containing more than one epoxy group per molecule of polyhydroxy compounds with epihalohydrins or precursors thereof of polyhydric phenols with chain extension or advancing agents
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/68—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the catalysts used
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G75/00—Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
- C08G75/02—Polythioethers
- C08G75/04—Polythioethers from mercapto compounds or metallic derivatives thereof
- C08G75/045—Polythioethers from mercapto compounds or metallic derivatives thereof from mercapto compounds and unsaturated compounds
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- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Epoxy Resins (AREA)
- Adhesives Or Adhesive Processes (AREA)
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| PCT/JP2022/047359 WO2024089905A1 (fr) | 2022-10-28 | 2022-12-22 | Composition de résine, adhésif, agent d'étanchéité, produit durci, dispositif à semi-conducteur et composant électronique |
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| JP2022173402A JP7217565B1 (ja) | 2022-10-28 | 2022-10-28 | 樹脂組成物、接着剤、封止材、硬化物、半導体装置及び電子部品 |
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Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2008001867A (ja) | 2006-06-26 | 2008-01-10 | Three Bond Co Ltd | 硬化性樹脂組成物 |
| WO2012164869A1 (fr) | 2011-05-31 | 2012-12-06 | 日油株式会社 | Composition de résine durcissable |
| JP2014141621A (ja) | 2013-01-25 | 2014-08-07 | Toyo Ink Sc Holdings Co Ltd | 紫外線硬化性組成物 |
| JP2017101112A (ja) | 2015-11-30 | 2017-06-08 | 味の素株式会社 | 光および熱硬化性樹脂組成物 |
| JP2018095829A (ja) | 2016-12-09 | 2018-06-21 | 日油株式会社 | 粘着剤組成物、及びこれを用いた積層体 |
| WO2021033329A1 (fr) | 2019-08-21 | 2021-02-25 | ナミックス株式会社 | Composition de résine époxy |
| JP2021075698A (ja) | 2019-10-31 | 2021-05-20 | 味の素株式会社 | 硬化性組成物 |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3367531B2 (ja) * | 1992-10-22 | 2003-01-14 | 味の素株式会社 | エポキシ樹脂組成物 |
| JP3367532B2 (ja) | 1992-10-22 | 2003-01-14 | 味の素株式会社 | エポキシ樹脂組成物 |
| JP2009051954A (ja) * | 2007-08-28 | 2009-03-12 | Three Bond Co Ltd | 光および加熱硬化性組成物とその硬化物 |
| JP2012153794A (ja) | 2011-01-26 | 2012-08-16 | Sakai Chem Ind Co Ltd | 樹脂組成物、樹脂硬化物および樹脂成形体 |
| CN103525315B (zh) * | 2012-06-29 | 2016-06-22 | 第一毛织株式会社 | 用于偏振板的粘合剂组合物、使用其的偏振板和光学元件 |
| KR101509483B1 (ko) * | 2013-09-26 | 2015-04-08 | 주식회사 신광화학산업 | 금속과 수지의 이종 재질간 고접착력이 유지되는 이중 경화형 에폭시 접착제 조성물을 이용한 금속과 수지의 접착 방법 |
| CN109153842A (zh) * | 2016-07-05 | 2019-01-04 | 积水保力马科技株式会社 | 密封材料组合物及密封材料 |
| JP2019156965A (ja) | 2018-03-13 | 2019-09-19 | ナミックス株式会社 | エポキシ樹脂組成物 |
| JP7226899B2 (ja) | 2018-04-27 | 2023-02-21 | ラピスセミコンダクタ株式会社 | 電子機器及び配線基板 |
| KR102271763B1 (ko) * | 2020-02-18 | 2021-07-01 | 한국기술교육대학교 산학협력단 | 열경화성 급속 경화 접착제 조성물 |
| JPWO2022210261A1 (fr) * | 2021-03-30 | 2022-10-06 |
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- 2022-10-28 JP JP2022173402A patent/JP7217565B1/ja active Active
- 2022-12-22 WO PCT/JP2022/047359 patent/WO2024089905A1/fr unknown
Patent Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2008001867A (ja) | 2006-06-26 | 2008-01-10 | Three Bond Co Ltd | 硬化性樹脂組成物 |
| WO2012164869A1 (fr) | 2011-05-31 | 2012-12-06 | 日油株式会社 | Composition de résine durcissable |
| JP2014141621A (ja) | 2013-01-25 | 2014-08-07 | Toyo Ink Sc Holdings Co Ltd | 紫外線硬化性組成物 |
| JP2017101112A (ja) | 2015-11-30 | 2017-06-08 | 味の素株式会社 | 光および熱硬化性樹脂組成物 |
| JP2018095829A (ja) | 2016-12-09 | 2018-06-21 | 日油株式会社 | 粘着剤組成物、及びこれを用いた積層体 |
| WO2021033329A1 (fr) | 2019-08-21 | 2021-02-25 | ナミックス株式会社 | Composition de résine époxy |
| JP2021075698A (ja) | 2019-10-31 | 2021-05-20 | 味の素株式会社 | 硬化性組成物 |
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| JP2024064648A (ja) | 2024-05-14 |
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