CN1037975C - 固化性环氧树脂悬浮液 - Google Patents
固化性环氧树脂悬浮液 Download PDFInfo
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- CN1037975C CN1037975C CN93108692A CN93108692A CN1037975C CN 1037975 C CN1037975 C CN 1037975C CN 93108692 A CN93108692 A CN 93108692A CN 93108692 A CN93108692 A CN 93108692A CN 1037975 C CN1037975 C CN 1037975C
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- epoxy
- resins
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Classifications
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- B32B5/02—Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts characterised by structural features of a fibrous or filamentary layer
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- C08G59/42—Polycarboxylic acids; Anhydrides, halides or low molecular weight esters thereof
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J151/00—Adhesives based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Adhesives based on derivatives of such polymers
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J151/00—Adhesives based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Adhesives based on derivatives of such polymers
- C09J151/04—Adhesives based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Adhesives based on derivatives of such polymers grafted on to rubbers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2260/00—Layered product comprising an impregnated, embedded, or bonded layer wherein the layer comprises an impregnation, embedding, or binder material
- B32B2260/02—Composition of the impregnated, bonded or embedded layer
- B32B2260/021—Fibrous or filamentary layer
- B32B2260/023—Two or more layers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2260/00—Layered product comprising an impregnated, embedded, or bonded layer wherein the layer comprises an impregnation, embedding, or binder material
- B32B2260/04—Impregnation, embedding, or binder material
- B32B2260/046—Synthetic resin
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2262/00—Composition or structural features of fibres which form a fibrous or filamentary layer or are present as additives
- B32B2262/10—Inorganic fibres
- B32B2262/101—Glass fibres
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2315/00—Other materials containing non-metallic inorganic compounds not provided for in groups B32B2311/00 - B32B2313/04
- B32B2315/08—Glass
- B32B2315/085—Glass fiber cloth or fabric
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2666/00—Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
- C08L2666/02—Organic macromolecular compounds, natural resins, waxes or and bituminous materials
- C08L2666/14—Macromolecular compounds according to C08L59/00 - C08L87/00; Derivatives thereof
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Epoxy Resins (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Adhesives Or Adhesive Processes (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH2161/92-0 | 1992-07-09 | ||
| CH216192 | 1992-07-09 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1083082A CN1083082A (zh) | 1994-03-02 |
| CN1037975C true CN1037975C (zh) | 1998-04-08 |
Family
ID=4227305
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN93108692A Expired - Fee Related CN1037975C (zh) | 1992-07-09 | 1993-07-08 | 固化性环氧树脂悬浮液 |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US6111015A (enExample) |
| EP (1) | EP0578613B1 (enExample) |
| JP (1) | JP3438059B2 (enExample) |
| KR (1) | KR100274526B1 (enExample) |
| CN (1) | CN1037975C (enExample) |
| CA (1) | CA2100026A1 (enExample) |
| DE (1) | DE59310074D1 (enExample) |
| ES (1) | ES2148213T3 (enExample) |
| FI (1) | FI110265B (enExample) |
| NO (1) | NO307470B1 (enExample) |
Families Citing this family (86)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ATE195544T1 (de) * | 1993-12-21 | 2000-09-15 | Ciba Sc Holding Ag | Zusammensetzungen auf der basis von epoxidharzen, zähigkeitsvermittlern und aminen |
| JPH0925393A (ja) * | 1995-05-09 | 1997-01-28 | Toray Ind Inc | 繊維強化複合材料用エポキシ樹脂組成物、プリプレグおよび繊維強化複合材料 |
| EP0776917B1 (de) | 1995-11-29 | 2002-05-29 | Vantico AG | Core/Shell-Partikel und diese enthaltende härtbare Epoxidharzzusammensetzungen |
| ES2210484T3 (es) | 1996-07-02 | 2004-07-01 | Vantico Ag | Endurecedores de resinas epoxi. |
| CN1089105C (zh) * | 1998-11-09 | 2002-08-14 | 南开大学 | 含刚性介晶基团及柔性链的环氧树脂粘合剂及其制备方法 |
| CA2365510A1 (en) | 1999-03-16 | 2000-09-21 | Vantico Ag | Hardenable composition with a particular combination of characteristics |
| JP4568940B2 (ja) * | 1999-04-13 | 2010-10-27 | 日立化成工業株式会社 | 封止用エポキシ樹脂組成物及び電子部品装置 |
| KR100785572B1 (ko) * | 1999-04-13 | 2007-12-13 | 히다치 가세고교 가부시끼가이샤 | 에폭시수지조성물 및 전자장치 |
| CN100371376C (zh) * | 2000-10-19 | 2008-02-27 | 长春人造树脂厂股份有限公司 | 阻燃性环氧树脂组合物及其应用 |
| JP5022540B2 (ja) * | 2001-01-15 | 2012-09-12 | コニカミノルタホールディングス株式会社 | インクジェットヘッド及びインクジェットヘッドの製造方法 |
| JP4771445B2 (ja) * | 2001-07-11 | 2011-09-14 | 日本化薬株式会社 | 電子部品用絶縁樹脂組成物及び接着シート |
| WO2003031493A1 (de) * | 2001-10-08 | 2003-04-17 | Vantico Gmbh & Co. Kg | Verfahren zur herstellung von rohren aus verbundwerkstoffen |
| CA2471368A1 (en) | 2001-12-21 | 2003-07-03 | Henkel Teroson Gmbh | Expandable epoxy resin-based systems modified with thermoplastic polymers |
| US20030198824A1 (en) * | 2002-04-19 | 2003-10-23 | Fong John W. | Photocurable compositions containing reactive polysiloxane particles |
| US6849687B2 (en) * | 2002-08-01 | 2005-02-01 | Bayer Polymers Llc | Thermoplastic composition having low gloss appearance |
| AU2003264513A1 (en) * | 2002-09-19 | 2004-04-08 | Mitsui Chemicals, Inc. | Sealing composition for liquid crystal displays and process for production of liquid crystal display panels |
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| DE10357355A1 (de) * | 2003-12-09 | 2005-07-14 | Henkel Kgaa | 2 K Klebstoffe für den Fahrzeugbau |
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| US7649060B2 (en) * | 2005-12-02 | 2010-01-19 | Henkel Corporation | Curable compositions |
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| GB0806434D0 (en) | 2008-04-09 | 2008-05-14 | Zephyros Inc | Improvements in or relating to structural adhesives |
| DE102008023076A1 (de) * | 2008-05-09 | 2009-11-12 | Henkel Ag & Co. Kgaa | Polymerisierbare Zusammensetzung |
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| US20100040838A1 (en) * | 2008-08-15 | 2010-02-18 | Abdallah David J | Hardmask Process for Forming a Reverse Tone Image |
| US20100183851A1 (en) * | 2009-01-21 | 2010-07-22 | Yi Cao | Photoresist Image-forming Process Using Double Patterning |
| US8084186B2 (en) | 2009-02-10 | 2011-12-27 | Az Electronic Materials Usa Corp. | Hardmask process for forming a reverse tone image using polysilazane |
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| CA2753852C (en) * | 2009-02-27 | 2014-05-06 | Momentive Specialty Chemicals Inc. | Compositions useful for non-cellulose fiber sizing, coating or binding compositions, and composites incorporating same |
| BRPI0924015A2 (pt) | 2009-04-21 | 2016-01-26 | Dow Global Technologies Llc | composição de agente de cura, composição curável e produto termofixo |
| CA2766859A1 (en) * | 2009-07-08 | 2011-01-13 | Henkel Ag & Co. Kgaa | Electrically conductive adhesives |
| US8518208B2 (en) * | 2009-08-31 | 2013-08-27 | Cytec Technology Corp. | High performance adhesive compositions |
| GB0916205D0 (en) | 2009-09-15 | 2009-10-28 | Zephyros Inc | Improvements in or relating to cavity filling |
| JP5605827B2 (ja) * | 2010-01-07 | 2014-10-15 | 株式会社カネカ | 不飽和エステル系樹脂組成物、不飽和エステル系硬化物、及びこれらの製造方法 |
| BR112012022319B1 (pt) | 2010-03-04 | 2020-01-28 | Zephyros Inc | laminado estrutural compósito |
| GB201007793D0 (en) | 2010-05-10 | 2010-06-23 | Zephyros Inc | Improvements in or relating to structural adhesives |
| NO2616520T3 (enExample) | 2010-09-15 | 2018-07-21 | ||
| GB201102672D0 (en) | 2011-02-15 | 2011-03-30 | Zephyros Inc | Improved structural adhesives |
| JP2012255135A (ja) * | 2011-05-17 | 2012-12-27 | Rohm & Haas Co | 熱可塑性ポリマーを吸収したラテックス粒子 |
| SG11201501745VA (en) * | 2012-09-07 | 2015-04-29 | Dow Global Technologies Llc | Toughened epoxy resin formulations |
| KR20150073173A (ko) * | 2012-10-17 | 2015-06-30 | 다우 글로벌 테크놀로지스 엘엘씨 | 코어 쉘 고무 개질된 고체 에폭시 수지 |
| JP2015532354A (ja) | 2012-10-19 | 2015-11-09 | ダウ グローバル テクノロジーズ エルエルシー | ポリオールを用いたポリマー粒子分散液 |
| US8981027B2 (en) | 2013-03-15 | 2015-03-17 | Henkel IP & Holding GmbH | Two-part, cyanoacrylate/cationically curable adhesive systems |
| US10240075B2 (en) | 2013-04-26 | 2019-03-26 | Zephyros, Inc. | Bonding dissimilar materials with adhesive paste |
| EP3024908B1 (en) * | 2013-07-24 | 2020-12-16 | Blue Cube IP LLC | Curable compositions |
| US10577522B2 (en) | 2013-07-26 | 2020-03-03 | Zephyros, Inc. | Thermosetting adhesive films including a fibrous carrier |
| EP3162842B1 (en) * | 2014-06-30 | 2019-04-17 | Mitsubishi Chemical Corporation | Tow prepreg, composite pressure vessel, and method for manufacturing same |
| WO2016039232A1 (ja) * | 2014-09-11 | 2016-03-17 | 株式会社カネカ | 注型用エポキシ樹脂組成物 |
| GB201417985D0 (en) | 2014-10-10 | 2014-11-26 | Zephyros Inc | Improvements in or relating to structural adhesives |
| DE102014226826A1 (de) | 2014-12-22 | 2016-06-23 | Henkel Ag & Co. Kgaa | Epoxidharz-Zusammensetzung |
| FR3031109B1 (fr) * | 2014-12-24 | 2018-08-17 | Arkema France | Composition de polymeres, son procede de preparation, son utilisation et composition la comprenant |
| MX2020008332A (es) | 2018-02-09 | 2020-09-21 | Ppg Ind Ohio Inc | Composiciones de recubrimiento. |
| CN111868170B (zh) | 2018-03-16 | 2024-08-06 | 亨斯迈先进材料许可(瑞士)有限公司 | 存储稳定且固化性的树脂组合物 |
| GB2576791B (en) | 2018-08-13 | 2022-09-14 | Henkel Ag & Co Kgaa | A two-part cyanoacrylate curable adhesive system |
| GB2576792B (en) | 2018-08-13 | 2022-09-14 | Henkel Ag & Co Kgaa | A two-part cyanoacrylate curable adhesive system |
| GB2582537B (en) | 2019-03-04 | 2022-02-23 | Henkel IP & Holding GmbH | Two-part, cyanoacrylate/cationically curable adhesive systems |
| DE102019204190A1 (de) * | 2019-03-27 | 2020-10-01 | Siemens Aktiengesellschaft | Gießharz, Formkörper daraus und Verwendung des Formkörpers |
| CN113631390A (zh) * | 2019-03-28 | 2021-11-09 | 汉高股份有限及两合公司 | 用于增材制造的可光固化的组合物 |
| EP3825355A1 (de) | 2019-11-22 | 2021-05-26 | Henkel AG & Co. KGaA | Formulierungen mit hohen glasübergangstemperaturen für laminate |
| EP3835378A1 (en) | 2019-12-13 | 2021-06-16 | Henkel AG & Co. KGaA | Two component (2k) curable adhesive composition |
| ES2973449T3 (es) * | 2019-12-13 | 2024-06-20 | Henkel Ag & Co Kgaa | Composición adhesiva curable de dos componentes (2K) |
| WO2022043160A1 (en) | 2020-08-27 | 2022-03-03 | Henkel Ag & Co. Kgaa | Electrically conductive one component (1k) epoxy formulation |
| CN114891161B (zh) * | 2022-05-26 | 2024-08-06 | 共享新材料(山东)有限公司 | 一种浆状复合材料及其制备方法和模具 |
| CN119731230A (zh) | 2022-06-28 | 2025-03-28 | 汉高股份有限及两合公司 | 水下粘合的方法 |
| WO2025135157A1 (ja) * | 2023-12-20 | 2025-06-26 | 株式会社カネカ | 硬化性樹脂組成物およびその利用 |
| GB2640960A (en) | 2024-05-10 | 2025-11-12 | Henkel Ag & Co Kgaa | Debonding of a cured composition |
Family Cites Families (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3496250A (en) * | 1967-02-21 | 1970-02-17 | Borg Warner | Blends of epoxy resins and acrylonitrile butadiene-styrene graft copolymers |
| DE2023473A1 (de) * | 1969-05-15 | 1970-11-19 | Shell Internationale Research Maatschappij N.V., Den Haag (Niederlande) | Verfahren zum Herstellen von gehärteten Epoxyharzprodukten mit hoher Schlagzähigkeit |
| JPS5137125B2 (enExample) * | 1971-08-30 | 1976-10-14 | ||
| US3864426A (en) * | 1973-05-23 | 1975-02-04 | Union Carbide Corp | Thermal shock resistant epoxy compositions |
| US4026970A (en) * | 1975-11-05 | 1977-05-31 | The B. F. Goodrich Company | Overpolymer rubbers as tougheners for thermoset and thermoplastic molding compounds and compositions thereof |
| CH606252A5 (enExample) * | 1977-01-07 | 1978-10-31 | Ciba Geigy Ag | |
| US4645803A (en) * | 1984-02-29 | 1987-02-24 | American Cyanamid Company | Curable epoxy resin compositions |
| US4537805A (en) * | 1984-03-26 | 1985-08-27 | W. R. Grace & Co. | Reactive plastisol dispersion |
| US4668736A (en) * | 1984-07-18 | 1987-05-26 | Minnesota Mining And Manufacturing Company | Fast curing epoxy resin compositions |
| CA1249691A (en) * | 1984-07-18 | 1989-01-31 | Janis Robins | Fast curing epoxy resin compositions |
| DE3674902D1 (de) * | 1985-06-26 | 1990-11-15 | Dow Chemical Co | Mit rubber modifizierte epoxyzusammensetzungen. |
| US4841010A (en) | 1987-09-02 | 1989-06-20 | State Of Israel, Ministry Of Defence, Armament Development Authorithy, Rafel | Triglycidyl ether/tetraglycidyl ether/alkadiene rubber/polyalkylene polyamine formulation |
| US4983672A (en) * | 1987-12-23 | 1991-01-08 | Minnesota Mining And Manufacturing Company | Epoxide resin compositions and method |
| US4846905A (en) * | 1988-04-06 | 1989-07-11 | Minnesota Mining And Manufacturing Company | Acid catalyzed, toughened epoxy adhesives |
| JP2717229B2 (ja) * | 1988-06-21 | 1998-02-18 | 旭化成工業株式会社 | 樹脂補強用ゴム粒子及び補強樹脂組成物 |
| US5075379A (en) | 1989-02-23 | 1991-12-24 | First Chemical Corporation | Rubber/diamine blends for use in curing epoxy resins |
| GB8926181D0 (en) * | 1989-11-20 | 1990-01-10 | Secr Defence | Rubber toughening epoxy resins |
| KR100193147B1 (ko) * | 1990-03-30 | 1999-06-15 | 월터클라웨인, 한느-피터 위트린 | 개질된 에폭시 수지 |
| USH1405H (en) * | 1992-04-09 | 1995-01-03 | Shell Oil Company | Epoxy resin composition |
| US5280067A (en) * | 1992-06-18 | 1994-01-18 | Minnesota Mining And Manufacturing Company | Substituted pentafluoroantmonic acid-substituted aniline epoxy curing catalysts |
| EP0576397B1 (de) * | 1992-06-25 | 1998-07-22 | Ciba SC Holding AG | Lagerstabile Suspension von Härtern und Zähigkeitsvermittlern für Epoxidharze |
-
1993
- 1993-06-30 DE DE59310074T patent/DE59310074D1/de not_active Expired - Lifetime
- 1993-06-30 ES ES93810462T patent/ES2148213T3/es not_active Expired - Lifetime
- 1993-06-30 EP EP93810462A patent/EP0578613B1/de not_active Expired - Lifetime
- 1993-07-07 CA CA002100026A patent/CA2100026A1/en not_active Abandoned
- 1993-07-07 FI FI933114A patent/FI110265B/fi not_active IP Right Cessation
- 1993-07-08 CN CN93108692A patent/CN1037975C/zh not_active Expired - Fee Related
- 1993-07-08 NO NO932499A patent/NO307470B1/no not_active IP Right Cessation
- 1993-07-08 KR KR1019930012799A patent/KR100274526B1/ko not_active Expired - Fee Related
- 1993-07-09 JP JP19418493A patent/JP3438059B2/ja not_active Expired - Fee Related
-
1995
- 1995-02-21 US US08/391,329 patent/US6111015A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| EP0578613A3 (enExample) | 1994-04-20 |
| NO932499L (no) | 1994-01-10 |
| KR100274526B1 (ko) | 2000-12-15 |
| JP3438059B2 (ja) | 2003-08-18 |
| EP0578613B1 (de) | 2000-07-12 |
| KR940002314A (ko) | 1994-02-17 |
| EP0578613A2 (de) | 1994-01-12 |
| US6111015A (en) | 2000-08-29 |
| FI933114L (fi) | 1994-01-10 |
| DE59310074D1 (de) | 2000-08-17 |
| CN1083082A (zh) | 1994-03-02 |
| NO932499D0 (no) | 1993-07-08 |
| FI110265B (fi) | 2002-12-31 |
| CA2100026A1 (en) | 1994-01-10 |
| NO307470B1 (no) | 2000-04-10 |
| ES2148213T3 (es) | 2000-10-16 |
| FI933114A0 (fi) | 1993-07-07 |
| JPH06157715A (ja) | 1994-06-07 |
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