JP4624784B2 - 放射線硬化性、無溶剤型および印刷可能な感圧接着剤前駆物質 - Google Patents
放射線硬化性、無溶剤型および印刷可能な感圧接着剤前駆物質 Download PDFInfo
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- JP4624784B2 JP4624784B2 JP2004515657A JP2004515657A JP4624784B2 JP 4624784 B2 JP4624784 B2 JP 4624784B2 JP 2004515657 A JP2004515657 A JP 2004515657A JP 2004515657 A JP2004515657 A JP 2004515657A JP 4624784 B2 JP4624784 B2 JP 4624784B2
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Images
Classifications
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- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
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- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F290/00—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups
- C08F290/02—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups on to polymers modified by introduction of unsaturated end groups
- C08F290/06—Polymers provided for in subclass C08G
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
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- C08F290/02—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups on to polymers modified by introduction of unsaturated end groups
- C08F290/06—Polymers provided for in subclass C08G
- C08F290/067—Polyurethanes; Polyureas
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- 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
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- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
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- C08G18/671—Unsaturated compounds having only one group containing active hydrogen
- C08G18/672—Esters of acrylic or alkyl acrylic acid having only one group containing active hydrogen
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- 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
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
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- Y10T428/2878—Adhesive compositions including addition polymer from unsaturated monomer
- Y10T428/2891—Adhesive compositions including addition polymer from unsaturated monomer including addition polymer from alpha-beta unsaturated carboxylic acid [e.g., acrylic acid, methacrylic acid, etc.] Or derivative thereof
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
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- Y10T428/31551—Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
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- Y10T428/31884—Regenerated or modified cellulose
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
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Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Macromonomer-Based Addition Polymer (AREA)
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| EP20020013604 EP1375617A1 (en) | 2002-06-19 | 2002-06-19 | Radiation-curable, solvent-free and printable precursor of a pressure-sensitive adhesive |
| PCT/US2003/013551 WO2004000961A1 (en) | 2002-06-19 | 2003-05-01 | Radiation-curable, solvent-free and printable precursor of a pressure-sensitive adhesive |
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| JP2005530024A JP2005530024A (ja) | 2005-10-06 |
| JP2005530024A5 JP2005530024A5 (enExample) | 2006-06-15 |
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| EP (2) | EP1375617A1 (enExample) |
| JP (1) | JP4624784B2 (enExample) |
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| AU (1) | AU2003232027A1 (enExample) |
| DE (1) | DE60307113T3 (enExample) |
| WO (1) | WO2004000961A1 (enExample) |
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| US7300619B2 (en) | 2000-03-13 | 2007-11-27 | Objet Geometries Ltd. | Compositions and methods for use in three dimensional model printing |
| US20030207959A1 (en) * | 2000-03-13 | 2003-11-06 | Eduardo Napadensky | Compositions and methods for use in three dimensional model printing |
| DE10049669A1 (de) * | 2000-10-06 | 2002-04-11 | Tesa Ag | Verfahren zur Herstellung von vernetzten Acrylatschmelzhaftklebemassen |
| US6949297B2 (en) | 2001-11-02 | 2005-09-27 | 3M Innovative Properties Company | Hybrid adhesives, articles, and methods |
| US6887917B2 (en) | 2002-12-30 | 2005-05-03 | 3M Innovative Properties Company | Curable pressure sensitive adhesive compositions |
| US7927703B2 (en) | 2003-04-11 | 2011-04-19 | 3M Innovative Properties Company | Adhesive blends, articles, and methods |
| US7691437B2 (en) * | 2003-10-31 | 2010-04-06 | 3M Innovative Properties Company | Method for preparing a pressure-sensitive adhesive |
| WO2007030584A1 (en) * | 2005-09-09 | 2007-03-15 | Dyna-Tech Adhesives, Incorporated | (meth)acrylate resin curable adhesive |
| CN101258213A (zh) | 2005-09-09 | 2008-09-03 | 艾利丹尼森公司 | 含有(甲基)丙烯酸酯树脂可固化胶粘剂的热收缩薄膜 |
| US8398306B2 (en) | 2005-11-07 | 2013-03-19 | Kraft Foods Global Brands Llc | Flexible package with internal, resealable closure feature |
| US20070197362A1 (en) * | 2006-02-02 | 2007-08-23 | Bridgestone Corporation | Conductive elastic roller and image forming apparatus comprising the same |
| US20070191506A1 (en) * | 2006-02-13 | 2007-08-16 | 3M Innovative Properties Company | Curable compositions for optical articles |
| US20080121341A1 (en) * | 2006-11-28 | 2008-05-29 | Applied Extrusion Technologies | Radiation curable adhesive with high molecular weight oligomer |
| JP4437502B2 (ja) * | 2007-04-03 | 2010-03-24 | 日東電工株式会社 | 塗膜保護用シート |
| US20080312354A1 (en) * | 2007-05-23 | 2008-12-18 | Karina Anne Krawczyk | Removable Radiation Cured Composition And Process For Protecting A Micro-Fluid Ejection Head |
| JP5135564B2 (ja) * | 2007-06-12 | 2013-02-06 | デクセリアルズ株式会社 | 接着剤組成物 |
| US9232808B2 (en) | 2007-06-29 | 2016-01-12 | Kraft Foods Group Brands Llc | Processed cheese without emulsifying salts |
| KR101662851B1 (ko) * | 2008-03-31 | 2016-10-05 | 쓰리엠 이노베이티브 프로퍼티즈 컴파니 | 다층 광학 필름용 접착제층 |
| WO2010079584A1 (ja) * | 2009-01-07 | 2010-07-15 | ディーエイチ・マテリアル株式会社 | 粘着剤及び粘着フィルム |
| JP5686518B2 (ja) * | 2010-01-25 | 2015-03-18 | 協立化学産業株式会社 | カメラモジュールの組立てに適した光硬化性接着組成物 |
| EP2353736A1 (en) | 2010-01-29 | 2011-08-10 | 3M Innovative Properties Company | Continuous process for forming a multilayer film and multilayer film prepared by such method |
| EP2539414A1 (en) | 2010-02-26 | 2013-01-02 | Kraft Foods Global Brands LLC | Reclosable package using low tack adhesive |
| RU2557614C2 (ru) * | 2010-02-26 | 2015-07-27 | Интерконтинентал Грейт Брэндс ЛЛС | Уф-отверждаемый самоклеющийся материал с низкой липкостью для повторно укупориваемых упаковок |
| CN102378539B (zh) * | 2010-08-18 | 2015-05-06 | 苏州天辅新型建材有限公司 | 一种在平板显示器框架上沉积缓冲材料的方法 |
| JP2013542455A (ja) * | 2010-08-18 | 2013-11-21 | スリーエム イノベイティブ プロパティズ カンパニー | 応力緩和光学接着剤を含む光学アセンブリ及びそれを作製する方法 |
| KR101351624B1 (ko) | 2010-12-31 | 2014-01-15 | 제일모직주식회사 | 광경화형 점착제 조성물 및 이를 이용한 모바일 폰의 모듈 조립 방법 |
| WO2012148608A1 (en) * | 2011-04-26 | 2012-11-01 | 3M Innovative Properties Company | Pressure-sensitive adhesives with mixed photocrosslinking system |
| EP2527383A1 (en) | 2011-05-27 | 2012-11-28 | Henkel AG & Co. KGaA | A process to manufacture thick layers of radiation cured adhesives |
| EP2548901A1 (en) * | 2011-07-19 | 2013-01-23 | Cytec Surface Specialties, S.A. | Process for the preparation of radiation curable compositions |
| CN102321437B (zh) * | 2011-07-25 | 2014-07-16 | 珠海保税区天然宝杰数码科技材料有限公司 | 一种uv固化装饰胶 |
| CN102898958B (zh) * | 2011-07-25 | 2016-11-02 | 汉高股份有限公司 | 一种粘合剂组合物 |
| EP2551024B1 (en) | 2011-07-29 | 2017-03-22 | 3M Innovative Properties Co. | Multilayer film having at least one thin layer and continuous process for forming such a film |
| EP2551313A1 (en) | 2011-07-29 | 2013-01-30 | 3M Innovative Properties Company | Multilayer pressure-sensitive adhesive film |
| EP2557132B1 (en) | 2011-08-10 | 2018-03-14 | 3M Innovative Properties Company | Multilayer adhesive film, in particular for bonding optical sensors |
| EP2581423A1 (en) | 2011-10-14 | 2013-04-17 | 3M Innovative Properties Company | Primerless multilayer adhesive film for bonding glass substrates |
| JP6024748B2 (ja) | 2012-04-27 | 2016-11-16 | 荒川化学工業株式会社 | 紫外線硬化型粘着剤組成物及び粘着層 |
| CN104768731B (zh) * | 2012-05-22 | 2018-06-19 | 汉高知识产权控股有限责任公司 | 用液态光学透明可光固化的粘合剂粘结基材的方法 |
| DE102013206624A1 (de) * | 2013-04-15 | 2014-10-16 | Tesa Se | Haftklebemasse und Verwendung derselben in einem Haftklebstreifen |
| KR101513080B1 (ko) * | 2013-09-16 | 2015-04-20 | 한국다이요잉크 주식회사 | 황화아연 미립자를 이용하는 잉크젯 마킹용 백색잉크 조성물 및 그 제조방법 |
| DE102014208111A1 (de) * | 2014-04-29 | 2015-10-29 | Tesa Se | Verfahren zur Herstellung einer Verklebung auf Permeat sensiblen Oberflächen |
| WO2016047268A1 (ja) * | 2014-09-26 | 2016-03-31 | 富士フイルム株式会社 | 活性エネルギー線硬化型粘着剤組成物、粘着シート |
| US9873180B2 (en) | 2014-10-17 | 2018-01-23 | Applied Materials, Inc. | CMP pad construction with composite material properties using additive manufacturing processes |
| US10875153B2 (en) | 2014-10-17 | 2020-12-29 | Applied Materials, Inc. | Advanced polishing pad materials and formulations |
| US9776361B2 (en) | 2014-10-17 | 2017-10-03 | Applied Materials, Inc. | Polishing articles and integrated system and methods for manufacturing chemical mechanical polishing articles |
| US11745302B2 (en) | 2014-10-17 | 2023-09-05 | Applied Materials, Inc. | Methods and precursor formulations for forming advanced polishing pads by use of an additive manufacturing process |
| KR102436416B1 (ko) | 2014-10-17 | 2022-08-26 | 어플라이드 머티어리얼스, 인코포레이티드 | 애디티브 제조 프로세스들을 이용한 복합 재료 특성들을 갖는 cmp 패드 구성 |
| JP6572417B2 (ja) * | 2014-12-25 | 2019-09-11 | 三菱ケミカル株式会社 | 光硬化性接着剤組成物及び積層体 |
| WO2016131742A1 (en) | 2015-02-20 | 2016-08-25 | Amcor Flexibles Burgdorf Gmbh | Reclosable packaging |
| ES2765202T3 (es) | 2015-02-20 | 2020-06-08 | Amcor Flexibles Burgdorf Gmbh | Embalaje que se puede volver a cerrar |
| WO2016131740A1 (en) * | 2015-02-20 | 2016-08-25 | Amcor Flexibles Burgdorf Gmbh | Reclosable packaging |
| TWI586780B (zh) * | 2015-03-23 | 2017-06-11 | 阿科瑪法國公司 | 壓敏性黏合劑 |
| FR3036288B1 (fr) * | 2015-05-21 | 2018-10-26 | Bertrand Perrin | Colles chirurgicales |
| JP6601494B2 (ja) * | 2015-06-15 | 2019-11-06 | 王子ホールディングス株式会社 | 粘着フィルム、積層体、及び加飾成形体 |
| US10618141B2 (en) | 2015-10-30 | 2020-04-14 | Applied Materials, Inc. | Apparatus for forming a polishing article that has a desired zeta potential |
| US10593574B2 (en) | 2015-11-06 | 2020-03-17 | Applied Materials, Inc. | Techniques for combining CMP process tracking data with 3D printed CMP consumables |
| US10391605B2 (en) | 2016-01-19 | 2019-08-27 | Applied Materials, Inc. | Method and apparatus for forming porous advanced polishing pads using an additive manufacturing process |
| JP6898715B2 (ja) * | 2016-08-01 | 2021-07-07 | デクセリアルズ株式会社 | 光硬化性樹脂組成物、画像表示装置、及び画像表示装置の製造方法 |
| US10259956B2 (en) | 2016-10-11 | 2019-04-16 | Xerox Corporation | Curable ink composition |
| WO2018118767A1 (en) | 2016-12-22 | 2018-06-28 | Avery Dennison Corporation | Convertible pressure sensitive adhesives comprising urethane (meth) acrylate oligomers |
| EP3607019B1 (en) | 2017-04-04 | 2023-12-27 | Arkema France | Curable compositions and low tack, self-adherent adhesives prepared therefrom |
| CN107030532A (zh) * | 2017-04-06 | 2017-08-11 | 东莞市华茂电子集团有限公司 | 一种五金壳直线点胶喷砂工艺 |
| WO2019016963A1 (ja) * | 2017-07-21 | 2019-01-24 | 日本化薬株式会社 | 紫外線硬化型接着剤、それを用いた貼り合せ方法及び物品 |
| US11471999B2 (en) | 2017-07-26 | 2022-10-18 | Applied Materials, Inc. | Integrated abrasive polishing pads and manufacturing methods |
| WO2019032286A1 (en) | 2017-08-07 | 2019-02-14 | Applied Materials, Inc. | ABRASIVE DISTRIBUTION POLISHING PADS AND METHODS OF MAKING SAME |
| CN107603531A (zh) * | 2017-08-30 | 2018-01-19 | 浙江欧丽数码喷绘材料有限公司 | 一种弱溶剂阻燃正喷灯片用阻燃胶水及其制备方法 |
| CN112154171B (zh) * | 2018-05-22 | 2023-06-13 | 3M创新有限公司 | 用增材制造技术处理可辐射固化的硫醇基组合物的方法 |
| CN108753242A (zh) * | 2018-06-25 | 2018-11-06 | 江苏科琪高分子材料研究院有限公司 | 用于显示模组柔性线路板和芯片粘结的光固化粘合剂组合物 |
| WO2020050932A1 (en) | 2018-09-04 | 2020-03-12 | Applied Materials, Inc. | Formulations for advanced polishing pads |
| EP3891200A1 (en) | 2018-12-03 | 2021-10-13 | Arkema France | Curable heat-seal adhesives for bonding polymers |
| CN111548739B (zh) | 2019-02-11 | 2022-03-01 | 3M创新有限公司 | 紫外光固化胶粘剂 |
| US11851570B2 (en) | 2019-04-12 | 2023-12-26 | Applied Materials, Inc. | Anionic polishing pads formed by printing processes |
| CN110283539A (zh) * | 2019-04-25 | 2019-09-27 | 中山布瑞特环保油墨有限公司 | 一种紫外光固化覆膜胶及其制备方法 |
| US11878389B2 (en) | 2021-02-10 | 2024-01-23 | Applied Materials, Inc. | Structures formed using an additive manufacturing process for regenerating surface texture in situ |
| ES2965171T3 (es) * | 2021-02-26 | 2024-04-11 | Sika Tech Ag | Un adhesivo acrílico sensible a la presión y su uso para proporcionar dispositivos de sellado autoadhesivos |
| TW202321401A (zh) * | 2021-08-02 | 2023-06-01 | 日商三菱化學股份有限公司 | 黏著劑組成物、黏著劑及黏著片 |
| CN114149780A (zh) * | 2021-11-15 | 2022-03-08 | 珠海天威新材料股份有限公司 | 可喷印uv压敏胶及其喷印方法、制品 |
| CN115029085A (zh) * | 2022-06-27 | 2022-09-09 | 赤壁凯利隆科技有限公司 | 一种电子束固化丙烯酸酯压敏胶及其制备方法 |
| CN115785875B (zh) * | 2022-12-26 | 2024-08-06 | 广州鹿山新材料股份有限公司 | 一种光学热熔胶膜及其制备方法和应用 |
| CN118638483B (zh) * | 2024-08-12 | 2024-12-13 | 博益鑫成高分子材料股份有限公司 | 一种增粘胶膜 |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4174307A (en) * | 1972-12-14 | 1979-11-13 | Polychrome Corporation | Room-temperature-radiation-curable polyurethane |
| JPS53285A (en) * | 1976-06-24 | 1978-01-05 | Gen Electric | Curable composition and coated substances |
| US4305854A (en) * | 1978-07-31 | 1981-12-15 | Polychrome Corporation | Radiation curable pressure sensitive adhesive |
| JPH01276447A (ja) * | 1988-04-27 | 1989-11-07 | Kuraray Co Ltd | 光記録媒体 |
| US5475038A (en) * | 1993-08-11 | 1995-12-12 | National Starch And Chemical Investment Holding Corporation | U.V. curable laminating adhesive composition |
| KR100454809B1 (ko) * | 1995-11-03 | 2005-01-15 | 코닌클리즈케 디에스엠 엔.브이. | 무용제방사선-경화성광학유리섬유코팅조성물및이를제조하는무용제방법 |
| JP2000082237A (ja) * | 1995-11-17 | 2000-03-21 | Taiyo Yuden Co Ltd | 光情報記録媒体 |
| DE19853813A1 (de) * | 1997-12-10 | 1999-06-17 | Henkel Kgaa | Klebstoff mit mehrstufiger Aushärtung und dessen Verwendung bei der Herstellung von Verbundmaterialien |
| US6180200B1 (en) * | 1998-06-01 | 2001-01-30 | Dsm N. V. | Cationic and hybrid radiation curable pressure sensitive adhesives for bonding of optical discs |
| JP3434216B2 (ja) * | 1998-08-28 | 2003-08-04 | 東亞合成株式会社 | 液晶高分子フィルムの接着用又は表面被覆用活性エネルギー線硬化型組成物 |
| JP2000345111A (ja) * | 1999-06-07 | 2000-12-12 | Three M Innovative Properties Co | 接着剤組成物及びそれを用いた光ディスク |
| JP2001226645A (ja) | 2000-02-18 | 2001-08-21 | Toppan Forms Co Ltd | 紫外線硬化型感圧接着剤およびそれを用いた感圧接着性プリント用シート |
| JP2002161124A (ja) * | 2000-11-28 | 2002-06-04 | Nippon Shokubai Co Ltd | ウレタン(メタ)アクリレート樹脂およびラジカル重合性樹脂組成物 |
| JP2002187906A (ja) * | 2000-12-21 | 2002-07-05 | Lintec Corp | 高分子量光重合開始剤及びそれを用いた光硬化性材料 |
| JP2003109251A (ja) * | 2001-07-27 | 2003-04-11 | Three M Innovative Properties Co | 光記録媒体及びその製造方法ならびに保護膜形成性樹脂材料 |
| JP2003268052A (ja) * | 2002-03-15 | 2003-09-25 | Toyobo Co Ltd | 活性エネルギー線反応型樹脂組成物、これを用いた粘接着剤、及び積層体 |
| EP1375618A1 (en) * | 2002-06-19 | 2004-01-02 | 3M Innovative Properties Company | Radiation-curable, solvent-free and printable precursor of an adhesive |
| US6887917B2 (en) * | 2002-12-30 | 2005-05-03 | 3M Innovative Properties Company | Curable pressure sensitive adhesive compositions |
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2002
- 2002-06-19 EP EP20020013604 patent/EP1375617A1/en not_active Withdrawn
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- 2003-05-01 US US10/513,125 patent/US7268173B2/en not_active Expired - Lifetime
- 2003-05-01 AU AU2003232027A patent/AU2003232027A1/en not_active Abandoned
- 2003-05-01 DE DE2003607113 patent/DE60307113T3/de not_active Expired - Lifetime
- 2003-05-01 EP EP03761019.3A patent/EP1539896B2/en not_active Expired - Lifetime
- 2003-05-01 AT AT03761019T patent/ATE334178T1/de not_active IP Right Cessation
- 2003-05-01 JP JP2004515657A patent/JP4624784B2/ja not_active Expired - Fee Related
- 2003-05-01 WO PCT/US2003/013551 patent/WO2004000961A1/en not_active Ceased
- 2003-05-01 CN CNB038142775A patent/CN1285689C/zh not_active Expired - Fee Related
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| US20050176842A1 (en) | 2005-08-11 |
| DE60307113T2 (de) | 2007-02-15 |
| EP1375617A1 (en) | 2004-01-02 |
| US7268173B2 (en) | 2007-09-11 |
| DE60307113D1 (de) | 2006-09-07 |
| EP1539896B2 (en) | 2013-11-06 |
| CN1285689C (zh) | 2006-11-22 |
| JP2005530024A (ja) | 2005-10-06 |
| EP1539896B1 (en) | 2006-07-26 |
| ATE334178T1 (de) | 2006-08-15 |
| DE60307113T3 (de) | 2014-04-30 |
| CN1662622A (zh) | 2005-08-31 |
| WO2004000961A1 (en) | 2003-12-31 |
| AU2003232027A1 (en) | 2004-01-06 |
| EP1539896A1 (en) | 2005-06-15 |
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