CN101903483B - 对玻璃粘合剂具有增强的粘合性的窗玻璃用保护涂层 - Google Patents
对玻璃粘合剂具有增强的粘合性的窗玻璃用保护涂层 Download PDFInfo
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- CN101903483B CN101903483B CN200880121503.7A CN200880121503A CN101903483B CN 101903483 B CN101903483 B CN 101903483B CN 200880121503 A CN200880121503 A CN 200880121503A CN 101903483 B CN101903483 B CN 101903483B
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Classifications
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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
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D201/00—Coating compositions based on unspecified macromolecular compounds
- C09D201/02—Coating compositions based on unspecified macromolecular compounds characterised by the presence of specified groups, e.g. terminal or pendant functional groups
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B60—VEHICLES IN GENERAL
- B60J—WINDOWS, WINDSCREENS, NON-FIXED ROOFS, DOORS, OR SIMILAR DEVICES FOR VEHICLES; REMOVABLE EXTERNAL PROTECTIVE COVERINGS SPECIALLY ADAPTED FOR VEHICLES
- B60J10/00—Sealing arrangements
- B60J10/30—Sealing arrangements characterised by the fastening means
- B60J10/34—Sealing arrangements characterised by the fastening means using adhesives
- B60J10/345—Sealing arrangements characterised by the fastening means using adhesives with formless adhesives, e.g. hot melt
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C17/00—Surface treatment of glass, not in the form of fibres or filaments, by coating
- C03C17/28—Surface treatment of glass, not in the form of fibres or filaments, by coating with organic material
- C03C17/30—Surface treatment of glass, not in the form of fibres or filaments, by coating with organic material with silicon-containing compounds
-
- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S525/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S525/901—Radial block
-
- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S525/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S525/925—Polymer from at least one nonethylenic monomer having terminal ethylenic unsaturation other than polyurethanes, polyesters, polyepoxides, aminoplasts, and phenoplasts
-
- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31551—Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
- Y10T428/31609—Particulate metal or metal compound-containing
- Y10T428/31612—As silicone, silane or siloxane
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Geochemistry & Mineralogy (AREA)
- General Chemical & Material Sciences (AREA)
- Mechanical Engineering (AREA)
- Wood Science & Technology (AREA)
- Paints Or Removers (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
- Polymerisation Methods In General (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Macromonomer-Based Addition Polymer (AREA)
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| US1454707P | 2007-12-18 | 2007-12-18 | |
| US61/014,547 | 2007-12-18 | ||
| PCT/US2008/087503 WO2009079647A1 (en) | 2007-12-18 | 2008-12-18 | Protective coating for window glass having enhanced adhesion to glass bonding adhesives |
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| CN101903483A CN101903483A (zh) | 2010-12-01 |
| CN101903483B true CN101903483B (zh) | 2014-09-10 |
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| EP (1) | EP2225339B1 (enExample) |
| JP (1) | JP5571572B2 (enExample) |
| KR (1) | KR101587666B1 (enExample) |
| CN (1) | CN101903483B (enExample) |
| BR (1) | BRPI0819414A2 (enExample) |
| WO (1) | WO2009079647A1 (enExample) |
Families Citing this family (67)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8617715B2 (en) * | 2003-12-06 | 2013-12-31 | Cpfilms Inc. | Fire retardant shades |
| US7781493B2 (en) | 2005-06-20 | 2010-08-24 | Dow Global Technologies Inc. | Protective coating for window glass |
| KR101139026B1 (ko) * | 2007-04-24 | 2012-04-26 | 다우 글로벌 테크놀로지스 엘엘씨 | 옥사졸라딘을 포함하는 1-성분 유리 하도제 |
| US20090181242A1 (en) * | 2008-01-11 | 2009-07-16 | Enniss James P | Exterior window film |
| CN102057010A (zh) * | 2008-04-11 | 2011-05-11 | 3M创新有限公司 | 单组分环氧基结构粘合剂 |
| US8286561B2 (en) | 2008-06-27 | 2012-10-16 | Ssw Holding Company, Inc. | Spill containing refrigerator shelf assembly |
| US11786036B2 (en) | 2008-06-27 | 2023-10-17 | Ssw Advanced Technologies, Llc | Spill containing refrigerator shelf assembly |
| WO2010042668A1 (en) | 2008-10-07 | 2010-04-15 | Ross Technology Corporation | Spill resistant surfaces having hydrophobic and oleophobic borders |
| JP5312602B2 (ja) * | 2008-10-29 | 2013-10-09 | ダウ グローバル テクノロジーズ エルエルシー | 長いオープンタイムを有するプライマーを含有する低エネルギー表面接着システム |
| CA2750305A1 (en) * | 2009-01-26 | 2010-07-29 | Sun Chemical Corporation | Uv curable ink for a plastic glazing system |
| DE102009018217A1 (de) | 2009-04-21 | 2010-11-11 | Basf Coatings Ag | Wasserfreie High-Solid-Basislacke, ihre Herstellung und ihre Verwendung zur Herstellung von Mehrschichtlackierungen, sowie Mehrschichtlackierungen enthaltend eine Basislackierung aus einem wasserfreien High-Solid-Basislack |
| DE102009018249A1 (de) * | 2009-04-21 | 2010-11-11 | Basf Coatings Ag | Mehrschicht-Beschichtung, deren Herstellung und Verwendung zur Verklebung von Glasscheiben |
| CN102498164B (zh) * | 2009-07-29 | 2015-08-19 | 拜尔材料科学股份公司 | 包括含丙烯酸酯涂层的多层产品 |
| ES2613885T3 (es) | 2009-11-04 | 2017-05-26 | Ssw Holding Company, Inc. | Superficies de aparatos de cocción que tienen un patrón de confinamiento de salpicaduras y procedimientos de fabricación de las mismas |
| GB2517341B (en) | 2009-11-16 | 2015-09-09 | Belron Hungary Kft Zug Branch | Glazing panel conditioning |
| MX2012010669A (es) | 2010-03-15 | 2013-02-07 | Ross Technology Corp | Destacadores y metodos para producir supreficies hidrofobas. |
| MX2013009609A (es) | 2011-02-21 | 2013-09-16 | Ross Technology Corp | Revestimiento suoerhidrofobos y oleofobos con sistemas aglutinantes con bajo contenido de compuestos organicos volatiles. |
| US8999509B2 (en) * | 2011-04-27 | 2015-04-07 | Cpfilms Inc. | Weather resistant exterior film composite |
| JP5818348B2 (ja) * | 2011-06-14 | 2015-11-18 | ベック株式会社 | 化粧壁面 |
| JP5846771B2 (ja) * | 2011-06-22 | 2016-01-20 | ベック株式会社 | 被覆方法 |
| US20140141262A1 (en) * | 2011-06-29 | 2014-05-22 | Sun Chemical Corporation | Vinyl alcohol polymers with silane side chains and compositions comprising the same |
| EP2581423A1 (en) | 2011-10-14 | 2013-04-17 | 3M Innovative Properties Company | Primerless multilayer adhesive film for bonding glass substrates |
| EP2631254A1 (en) | 2012-02-27 | 2013-08-28 | Cytec Surface Specialties, S.A. | Fluorinated water-oil repellency agents |
| EP2583986A1 (en) | 2011-10-17 | 2013-04-24 | Cytec Surface Specialties, S.A. | Fluorinated water-oil repellency agents |
| DE102011085428A1 (de) | 2011-10-28 | 2013-05-02 | Schott Ag | Einlegeboden |
| EP2791255B1 (en) | 2011-12-15 | 2017-11-01 | Ross Technology Corporation | Composition and coating for superhydrophobic performance |
| DE102012204290A1 (de) * | 2012-03-19 | 2013-09-19 | Evonik Degussa Gmbh | Addukte aus Isocyanatoalkyl-trialkoxysilanen und aliphatischen, alkyl-verzweigten Diolen oder Polyolen |
| CN104520392A (zh) | 2012-06-25 | 2015-04-15 | 罗斯科技公司 | 具有疏水和/或疏油性质的弹性体涂层 |
| JP6034623B2 (ja) * | 2012-08-29 | 2016-11-30 | 株式会社ブリヂストン | 重合触媒組成物の製造方法及び重合触媒組成物 |
| DE102013017300A1 (de) * | 2013-10-18 | 2015-04-23 | Konrad Hornschuch Ag | Prägewalze |
| CN106164187A (zh) | 2014-04-10 | 2016-11-23 | 3M创新有限公司 | 增粘和/或抑尘涂层 |
| KR101496160B1 (ko) * | 2014-09-25 | 2015-02-26 | (주)삼광기업 | 난스틱 세라믹 코팅 조성물 및 이를 코팅한 가열조리기구 |
| KR102386997B1 (ko) | 2015-12-30 | 2022-04-14 | 엘지디스플레이 주식회사 | 투명 접착제 조성물, 투명 접착층 및 이를 포함하는 표시장치 |
| EP3417024B1 (en) | 2016-02-19 | 2020-08-05 | Avery Dennison Corporation | Two stage methods for processing adhesives and related compositions |
| US10351726B2 (en) * | 2016-05-19 | 2019-07-16 | Dongwoo Fine-Chem Co., Ltd. | Hard coating composition and hard coating film using the same |
| CN106398431A (zh) * | 2016-08-31 | 2017-02-15 | 三棵树涂料股份有限公司 | 专用于玻璃的高附着力uv漆及其制备方法 |
| WO2018081268A1 (en) | 2016-10-25 | 2018-05-03 | Avery Dennison Corporation | Block polymers with photoinitiator groups in backbone and their use in adhesive compositions |
| US11066562B2 (en) | 2017-01-31 | 2021-07-20 | Hewlett-Packard Development Company, L.P. | Acrylamide-containing photo active co-solvents |
| KR102024162B1 (ko) * | 2017-06-28 | 2019-09-23 | 엘지전자 주식회사 | 유리 조성물 및 조리기기 |
| US10338287B2 (en) * | 2017-08-29 | 2019-07-02 | Southwall Technologies Inc. | Infrared-rejecting optical products having pigmented coatings |
| US11747532B2 (en) | 2017-09-15 | 2023-09-05 | Southwall Technologies Inc. | Laminated optical products and methods of making them |
| JP2021504524A (ja) * | 2017-11-27 | 2021-02-15 | ヘンケル アイピー アンド ホールディング ゲゼルシャフト ミット ベシュレンクテル ハフツング | ポリシロキサンウレタン化合物および光学的透明接着剤組成物 |
| JP2021504525A (ja) * | 2017-11-27 | 2021-02-15 | ヘンケル アイピー アンド ホールディング ゲゼルシャフト ミット ベシュレンクテル ハフツング | ポリシロキサンウレタン化合物および光学的透明接着剤組成物 |
| WO2019126327A1 (en) | 2017-12-19 | 2019-06-27 | Avery Dennison Corporation | Post-polymerization functionalization of pendant functional groups |
| EP3524582A1 (en) * | 2018-02-08 | 2019-08-14 | Surfix B.V. | Process for modification of a solid surface |
| US10613261B2 (en) | 2018-04-09 | 2020-04-07 | Southwall Technologies Inc. | Selective light-blocking optical products having a neutral reflection |
| US10627555B2 (en) | 2018-04-09 | 2020-04-21 | Southwall Technologies Inc. | Selective light-blocking optical products having a neutral reflection |
| CN108715752B (zh) * | 2018-06-22 | 2021-09-28 | 瑞洲树脂(东莞)有限公司 | 一种光与热双固化镜片、镜头填充胶 |
| CN109722161B (zh) * | 2018-12-29 | 2021-06-22 | 上海乘鹰新材料有限公司 | 高耐磨滑爽转印胶及其涂层的制备方法 |
| US20220135852A1 (en) * | 2019-02-22 | 2022-05-05 | Commscope Technologies Llc | Tack reduction for silicone gel seals |
| US20220185949A1 (en) * | 2019-04-25 | 2022-06-16 | 3M Innovative Properties Company | Adhesion promoters for structural adhesive applications |
| CN114788075A (zh) * | 2019-12-09 | 2022-07-22 | 洛德公司 | 用于介电绝缘的紫外线涂层 |
| KR102702298B1 (ko) * | 2019-12-16 | 2024-09-19 | 삼성디스플레이 주식회사 | 커버 윈도우 및 이를 포함하는 표시 장치 |
| EP3848431A1 (en) * | 2020-01-09 | 2021-07-14 | tesa SE | Adhesive printing form attachment layer, method for its manufacture, and printing form attachment cylinder comprising the same |
| CN111171751B (zh) * | 2020-01-21 | 2022-03-18 | 安徽富印新材料有限公司 | 一种uv减粘膜及其制备方法 |
| US11624007B2 (en) | 2020-01-29 | 2023-04-11 | Prc-Desoto International, Inc. | Photocurable adhesion-promoting compositions and methods of use |
| JP7217977B2 (ja) * | 2020-02-04 | 2023-02-06 | アジア原紙株式会社 | 活性エネルギー線硬化型組成物 |
| EP4127086A4 (en) * | 2020-03-26 | 2024-03-27 | Michelman, Inc. | Low-blushing coating formulations and associated uses |
| EP4150012A4 (en) | 2020-05-15 | 2024-08-28 | Swimc Llc | THERMOCURRING UNDERCOAT COMPOSITIONS COMPATIBLE WITH A RADICALLY CURED COATING FOR METAL SUBSTRATES |
| GB2611825A (en) * | 2021-10-18 | 2023-04-19 | Fenzi Agt Netherlands B V | Ultraviolet curable enamel compositions |
| WO2023242860A1 (en) * | 2022-06-16 | 2023-12-21 | Saint-Gobain Glass France | A decorative glass article with uniform sparkle effect |
| CN115386334B (zh) * | 2022-09-03 | 2024-06-04 | 烟台德邦科技股份有限公司 | 一种可uv湿气双固化的有机聚硅氧烷组合物及其制备方法 |
| CN115651527A (zh) * | 2022-09-13 | 2023-01-31 | 华容县恒兴建材有限公司 | 超哑肤感紫外光固化涂料及其制备方法和固化方法 |
| CN117167480B (zh) * | 2023-11-02 | 2024-01-30 | 浙江葆润应用材料有限公司 | 一种金属复合硅胶结构的密封圈 |
| WO2025170770A1 (en) * | 2024-02-05 | 2025-08-14 | Dow Global Technologies Llc | Thermally conductive compositions |
| CN118479749B (zh) * | 2024-05-09 | 2025-08-08 | 珠海水发兴业新材料科技有限公司 | 一种变色薄膜复合结构及其制备方法 |
| CN119529754B (zh) * | 2024-12-06 | 2025-09-30 | 广州白云科技股份有限公司 | 一种单组分加成型有机硅粘接胶及其制备方法 |
Family Cites Families (147)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3152162A (en) * | 1959-07-29 | 1964-10-06 | Bayer Ag | Polyisocyanate-carbodiimide adducts and process for the production thereof |
| US3743626A (en) * | 1968-10-18 | 1973-07-03 | Rohm & Haas | Hydrocurable oxazolidine-isocyanate compositions |
| US3549396A (en) * | 1969-08-13 | 1970-12-22 | Ppg Industries Inc | Method for producing pigments of improved dispersibility |
| US3971751A (en) * | 1975-06-09 | 1976-07-27 | Kanegafuchi Kagaku Kogyo Kabushiki Kaisha | Vulcanizable silylether terminated polymer |
| US4325012A (en) * | 1975-10-01 | 1982-04-13 | Franklin Electric Co., Inc. | Start winding cut-out circuit for an electric motor |
| US4218513A (en) * | 1977-06-28 | 1980-08-19 | Union Carbide Corporation | Polymer composite articles containing amino substituted mercapto organo silicon coupling agents |
| US4232088A (en) * | 1978-04-12 | 1980-11-04 | General Electric Company | Polycarbonate articles coated with an adherent, durable organopolysiloxane coating and process for producing same |
| US4302503A (en) | 1978-05-17 | 1981-11-24 | Libbey-Owens-Ford Company | Architectural spandrel |
| US4368236A (en) | 1978-11-30 | 1983-01-11 | General Electric Co. | Silicone resin coating compositions |
| JPS56109847A (en) * | 1980-01-29 | 1981-08-31 | Kanegafuchi Chem Ind Co Ltd | Primer composition |
| US4394491A (en) * | 1980-10-08 | 1983-07-19 | The Dow Chemical Company | Addition polymerizable adduct of a polymeric monoahl and an unsaturated isocyanate |
| US4345053A (en) * | 1981-07-17 | 1982-08-17 | Essex Chemical Corp. | Silicon-terminated polyurethane polymer |
| US4374210A (en) * | 1981-09-18 | 1983-02-15 | The Upjohn Company | Polyurea-polyurethane from a mixture of a polyol, an aromatic diamine, and an isocyanate-terminated prepolymer |
| US4374237A (en) * | 1981-12-21 | 1983-02-15 | Union Carbide Corporation | Silane-containing isocyanate-terminated polyurethane polymers |
| US4385133A (en) * | 1982-06-07 | 1983-05-24 | The Upjohn Company | Novel compositions and process |
| US4584245A (en) * | 1982-06-08 | 1986-04-22 | Asahi Glass Company Ltd. | Laminated safety glass |
| JPS59197401A (ja) * | 1983-04-26 | 1984-11-09 | Nippon Oil & Fats Co Ltd | 光重合開始剤 |
| US4839122A (en) | 1983-09-26 | 1989-06-13 | Libbey-Owens-Ford Co. | Reaction injection molding of window gasket |
| CA1259090A (en) | 1983-09-26 | 1989-09-05 | Libbey-Owens-Ford Co. | Preformed window assembly and method of making the same |
| DE3400860A1 (de) * | 1984-01-12 | 1985-07-18 | Henkel KGaA, 4000 Düsseldorf | Glasprimer |
| DE3407031A1 (de) * | 1984-02-27 | 1985-09-05 | Gurit-Essex, Freienbach | Chemisch haertende zweikomponentenmasse auf der basis von polyurethanen, verfahren zur herstellung einer haertbaren masse auf polyurethanbasis und verwendung von mischungen aus zwei komponenten auf polyurethanbasis |
| JPS60228516A (ja) * | 1984-04-26 | 1985-11-13 | Kanegafuchi Chem Ind Co Ltd | 新規重合体の製造法 |
| US4522975A (en) * | 1984-06-01 | 1985-06-11 | Olin Corporation | Select NCO-terminated, uretdione group-containing polyurethane prepolymers and lignocellulosic composite materials prepared therefrom |
| DE3587828T2 (de) * | 1984-07-26 | 1994-09-29 | Kanegafuchi Chemical Ind | Vernetzbare Polymerzusammensetzung. |
| US4610115A (en) | 1984-12-17 | 1986-09-09 | Ppg Industries, Inc. | Multiple-glazed combination vision and spandrel architectural panel and curtainwall |
| US4622369A (en) | 1985-04-30 | 1986-11-11 | Ppg Industries, Inc. | Urethane resins containing hydrolyzable moieties from organosilane compounds |
| US4645816A (en) | 1985-06-28 | 1987-02-24 | Union Carbide Corporation | Novel vulcanizable silane-terminated polyurethane polymers |
| US4625012A (en) | 1985-08-26 | 1986-11-25 | Essex Specialty Products, Inc. | Moisture curable polyurethane polymers |
| US4687533A (en) * | 1985-08-26 | 1987-08-18 | Essex Specialty Products, Inc. | Bonding method employing moisture curable polyurethane polymers |
| FR2591587A1 (fr) | 1985-12-17 | 1987-06-19 | Saint Gobain Vitrage | Film organo-mineral depose sur un substrat en verre eventuellement revetu d'une ou plusieurs couches metalliques minces. |
| JPS62146957A (ja) * | 1985-12-20 | 1987-06-30 | Nippon Shokubai Kagaku Kogyo Co Ltd | 硬化性被膜形成材 |
| DE3545899C1 (de) * | 1985-12-23 | 1987-04-23 | Gurit Essex Ag | Verfahren und Vorrichtung zum Auftragen einer mindestens zwei Komponenten umfassenden Klebe-,Dichtungs-,Versiegelungs- oder Beschichtungsmasse auf einen Gegenstand |
| US4697026A (en) * | 1986-01-06 | 1987-09-29 | Dow Corning Corporation | Acryl functional silicone compounds |
| US4643794A (en) * | 1986-03-04 | 1987-02-17 | Ashland Oil, Inc. | Primer and sealant for glass and coated metal |
| US4772716A (en) * | 1986-07-14 | 1988-09-20 | Ciba-Geigy Corporation | Oxazolidines containing silane groups |
| US4837274A (en) | 1986-09-30 | 1989-06-06 | Kanegafuchi Kagaku Kogyo Kabushiki Kaisha | Curable composition |
| US4758648A (en) | 1986-10-20 | 1988-07-19 | Essex Specialty Products, Inc. | High speed cure sealant |
| GB8705801D0 (en) * | 1987-03-11 | 1987-04-15 | Ici Plc | Injection moulding compositions |
| US4792316A (en) * | 1987-04-10 | 1988-12-20 | David Skedeleski | Surfboard protective tip |
| US4950581A (en) | 1987-07-06 | 1990-08-21 | Fuji Photo Film Co., Ltd. | Photopolymerizable composition |
| US4822680A (en) * | 1987-08-28 | 1989-04-18 | American Temporing, Inc. | Polyurethane visionary laminate glass and method of manufacture |
| JP2752070B2 (ja) * | 1987-12-05 | 1998-05-18 | 鐘淵化学工業株式会社 | 硬化性密封剤組成物 |
| CA1338943C (en) | 1987-12-28 | 1997-02-25 | Sadao Yukimoto | Curable composition of oxyalkylene polymer |
| JP2610305B2 (ja) | 1988-06-10 | 1997-05-14 | 鐘淵化学工業株式会社 | 硬化性組成物 |
| JP2557469B2 (ja) | 1988-06-10 | 1996-11-27 | 鐘淵化学工業株式会社 | 硬化性組成物 |
| US5175201A (en) * | 1988-10-31 | 1992-12-29 | American Cyanamid Company | Vinyl-terminated carbamylmethylated melamines, vinyl-terminated polyurethane/polyamide polymers and coating/adhesive compositions containing same |
| EP0376890A3 (de) * | 1988-12-29 | 1991-04-10 | Ciba-Geigy Ag | Silangruppenhaltige Oxazolidine |
| US5221560A (en) | 1989-02-17 | 1993-06-22 | Swedlow, Inc. | Radiation-curable coating compositions that form transparent, abrasion resistant tintable coatings |
| IT1229257B (it) * | 1989-05-11 | 1991-07-26 | Enichem Sintesi | Composti silicio organici contenenti un gruppo oxazolidinico |
| US5409995A (en) | 1989-05-29 | 1995-04-25 | Kanegafuchi Chemical Industry Co., Ltd. | Curing agent, preparation thereof and curable composition comprising the same |
| US5063269A (en) | 1990-01-16 | 1991-11-05 | Essex Specialty Products, Inc. | One-part primerless adhesive |
| US5167899A (en) * | 1990-07-07 | 1992-12-01 | The Dow Chemical Company | Process for melt blowing microfibers of rigid polyurethane having hard segments |
| US5114989A (en) * | 1990-11-13 | 1992-05-19 | The Dow Chemical Company | Isocyanate-terminated prepolymer and polyurethane foam prepared therefrom |
| US5266715A (en) | 1991-03-06 | 1993-11-30 | Ciba-Geigy Corporation | Glass coating with improved adhesion and weather resistance |
| AU664827B2 (en) | 1991-05-03 | 1995-12-07 | Raisio Benecol Ltd. | A substance for lowering high cholesterol level in serum and a method for preparing the same |
| JP2995308B2 (ja) | 1991-09-09 | 1999-12-27 | 鐘淵化学工業株式会社 | 硬化性組成物 |
| JP3002925B2 (ja) | 1992-04-08 | 2000-01-24 | 鐘淵化学工業株式会社 | 硬化性組成物 |
| WO1994009046A1 (en) | 1992-10-13 | 1994-04-28 | Essex Specialty Products, Inc. | Polyurethane sealant compositions |
| JP2782405B2 (ja) * | 1992-12-14 | 1998-07-30 | 信越化学工業株式会社 | 硬化性オルガノポリシロキサン組成物 |
| FR2699529B1 (fr) * | 1992-12-18 | 1995-02-03 | Saint Gobain Vitrage Int | Procédé de traitement d'un vitrage pour l'adhésion d'un profil périphérique. |
| US5314980A (en) | 1993-01-19 | 1994-05-24 | Minnesota Mining And Manufacturing Company | Epoxy coating compositions with metal-containing stabilizers |
| JP3250690B2 (ja) | 1993-04-12 | 2002-01-28 | 鐘淵化学工業株式会社 | 硬化性組成物 |
| US5409955A (en) | 1993-05-13 | 1995-04-25 | Bockow; Barry I. | Compositions and methods for inhibiting uterine contractility |
| ES2111936T3 (es) * | 1993-06-03 | 1998-03-16 | Gurit Essex Ag | Composicion imprimadora para mejorar la union de un adhesivo de uretano a sustratos no porosos. |
| US5664041A (en) * | 1993-12-07 | 1997-09-02 | Dsm Desotech, Inc. | Coating system for glass adhesion retention |
| CA2141515A1 (en) | 1994-02-08 | 1995-08-09 | John D. Blizzard | Abrasion-resistant coating |
| US5502145A (en) | 1994-03-02 | 1996-03-26 | Dsm Desotech. Inc. | Coating system for glass strength retention |
| JP3883215B2 (ja) | 1994-03-25 | 2007-02-21 | 株式会社カネカ | コンタクト型接着剤 |
| JP3361180B2 (ja) | 1994-04-28 | 2003-01-07 | セントラル硝子株式会社 | 撥水性紫外線赤外線吸収ガラス及びその製法 |
| CA2141516A1 (en) | 1994-06-13 | 1995-12-14 | John D. Blizzard | Radiation-curable oligomer-based coating composition |
| JP3292348B2 (ja) | 1994-10-11 | 2002-06-17 | ジェイエスアール株式会社 | 液状硬化性樹脂組成物 |
| AU695750B2 (en) | 1995-01-13 | 1998-08-20 | Essex Specialty Products Inc. | Two-part moisture curable polyurethane adhesive |
| DE69629053T2 (de) | 1995-01-13 | 2004-04-22 | Minnesota Mining And Mfg. Co., St. Paul | Verfahren und Zusammensetzung zum Verbinden von Komponenten mit Glas |
| DE69601316T2 (de) * | 1995-02-28 | 1999-08-26 | Dow Corning Corp. | Verfahren zur Herstellung organomodifizierter strahlungshärtbarer Silikonharze |
| US5976702A (en) | 1995-04-25 | 1999-11-02 | Asahi Glass Company Ltd. | Composition for surface treatment |
| DE19535936A1 (de) | 1995-09-27 | 1997-04-03 | Basf Lacke & Farben | Acryliertes Polyetherpolyol und dessen Verwendung für strahlenhärtbare Formulierungen |
| AR005429A1 (es) * | 1996-01-11 | 1999-06-23 | Essex Specialty Prod | Prepolimeros de poliuretano, composiciones adhesivas en un solo envase que incluyen dichos prepolimeros y procedimiento para adherir substratos con dichascomposiciones |
| US5922809A (en) | 1996-01-11 | 1999-07-13 | The Dow Chemical Company | One-part moisture curable polyurethane adhesive |
| FR2743802B1 (fr) | 1996-01-19 | 1998-03-20 | Saint Gobain Vitrage | Vitrage feuillete et primaire utilise pour sa realisation |
| US5786096A (en) | 1996-11-12 | 1998-07-28 | Asahi Glass Company Ltd. | Surface-treated substrate and process for its production |
| JP3634592B2 (ja) | 1997-01-08 | 2005-03-30 | セイコーエプソン株式会社 | 接着固定物、電子機器および時計 |
| US5852137A (en) | 1997-01-29 | 1998-12-22 | Essex Specialty Products | Polyurethane sealant compositions |
| US6228433B1 (en) * | 1997-05-02 | 2001-05-08 | Permagrain Products, Inc. | Abrasion resistant urethane coatings |
| US6582999B2 (en) | 1997-05-12 | 2003-06-24 | Silicon Genesis Corporation | Controlled cleavage process using pressurized fluid |
| US6093455A (en) * | 1997-05-23 | 2000-07-25 | Deco Patents, Inc. | Method and compositions for decorating glass |
| JP2002500670A (ja) | 1997-05-27 | 2002-01-08 | ファースト・ケミカル・コーポレイション | 芳香族マレイミド類およびその使用方法 |
| US5977202A (en) | 1997-09-22 | 1999-11-02 | Dsm N.V. | Radiation-curable compositions having fast cure speed and good adhesion to glass |
| US6080817A (en) * | 1997-12-08 | 2000-06-27 | Basf Corporation | Epoxy-urethane imine and hydroxyl primer |
| US5948927A (en) * | 1998-04-01 | 1999-09-07 | Witco Corporation | Bis-silyl tertiary amines |
| US6140445A (en) * | 1998-04-17 | 2000-10-31 | Crompton Corporation | Silane functional oligomer |
| US6828403B2 (en) * | 1998-04-27 | 2004-12-07 | Essex Specialty Products, Inc. | Method of bonding a window to a substrate using a silane functional adhesive composition |
| ATE252611T1 (de) | 1998-04-27 | 2003-11-15 | Essex Specialty Prod | Verfahren zur fixierung eines fensters an einem substrat unter verwendung von einer silanfunktionellen klebstoffzusammensetzung |
| US6245833B1 (en) | 1998-05-04 | 2001-06-12 | 3M Innovative Properties | Ceramer composition incorporating fluoro/silane component and having abrasion and stain resistant characteristics |
| SG77689A1 (en) | 1998-06-26 | 2001-01-16 | Ciba Sc Holding Ag | New o-acyloxime photoinitiators |
| US6008305A (en) * | 1998-06-30 | 1999-12-28 | Adco Products, Inc. | Primer for improving the bonding of adhesives to nonporous substrates |
| CA2337443A1 (en) | 1998-07-31 | 2000-02-10 | Ppg Industries Ohio, Inc. | Transparency with coating having primer for edge seal |
| CN1223646C (zh) | 1999-02-05 | 2005-10-19 | 陶氏环球技术公司 | 聚氨酯密封剂组合物 |
| US6309755B1 (en) | 1999-06-22 | 2001-10-30 | Exatec, Llc. | Process and panel for providing fixed glazing for an automotive vehicle |
| US6510872B1 (en) * | 1999-07-07 | 2003-01-28 | Wayn-Tex, Incorporated | Carpet backing and methods of making and using the same |
| US6623791B2 (en) | 1999-07-30 | 2003-09-23 | Ppg Industries Ohio, Inc. | Coating compositions having improved adhesion, coated substrates and methods related thereto |
| JP4917196B2 (ja) | 1999-09-24 | 2012-04-18 | Jsr株式会社 | 樹脂組成物及びその硬化物 |
| US6461419B1 (en) | 1999-11-01 | 2002-10-08 | 3M Innovative Properties Company | Curable inkjet printable ink compositions |
| DE19961632A1 (de) * | 1999-12-14 | 2001-06-28 | Inst Oberflaechenmodifizierung | Kit zur Beschichtung von Oberflächen, strahlenhärtbares Beschichtungsmittel und Verfahren zur Erzeugung von kratz-, abrieb- und haftfesten Beschichtungen |
| US6438306B1 (en) * | 2000-04-07 | 2002-08-20 | Dsm N.V. | Radiation curable resin composition |
| US20010041782A1 (en) * | 2000-01-12 | 2001-11-15 | Hiroyuki Okuhira | Novel latent curing agent and moisture-curable epoxy resin composition |
| JP2002012635A (ja) | 2000-06-28 | 2002-01-15 | Nippon Sheet Glass Co Ltd | 鏡の背面コート用紫外線硬化性樹脂組成物及びこの組成物で背面コートされた鏡 |
| WO2002038688A2 (en) | 2000-11-09 | 2002-05-16 | 3M Innovative Properties Company | Weather resistant, ink jettable, radiation curable, fluid compositions particularly suitable for outdoor applications |
| EP1217049A1 (de) * | 2000-12-23 | 2002-06-26 | Sika AG, vorm. Kaspar Winkler & Co. | Voranstrich für Beton |
| JP3788911B2 (ja) | 2001-02-07 | 2006-06-21 | 信越化学工業株式会社 | オルガノポリシロキサン組成物 |
| JP4670171B2 (ja) | 2001-04-18 | 2011-04-13 | 横浜ゴム株式会社 | プライマー組成物 |
| JP4423808B2 (ja) | 2001-04-18 | 2010-03-03 | 横浜ゴム株式会社 | プライマー組成物 |
| US6617371B2 (en) | 2001-06-08 | 2003-09-09 | Addison Clear Wave, Llc | Single component room temperature stable heat-curable acrylate resin adhesive |
| US6592998B2 (en) * | 2001-07-31 | 2003-07-15 | Ppg Industries Ohio, Inc. | Multi-layer composites formed from compositions having improved adhesion, coating compositions, and methods related thereto |
| US6641923B2 (en) | 2001-07-31 | 2003-11-04 | Ppg Industries Ohio, Inc. | Weldable coating compositions having improved intercoat adhesion |
| US6592999B1 (en) * | 2001-07-31 | 2003-07-15 | Ppg Industries Ohio, Inc. | Multi-layer composites formed from compositions having improved adhesion, coating compositions, and methods related thereto |
| JP2003128988A (ja) | 2001-10-23 | 2003-05-08 | Dainippon Ink & Chem Inc | 湿気硬化型プライマー |
| US6984287B2 (en) | 2001-11-02 | 2006-01-10 | The Dow Chemical Company | Primer composition for promoting adhesion of a urethane adhesive to a polymeric substrate |
| US6720380B2 (en) * | 2001-11-27 | 2004-04-13 | E. I. Du Pont De Nemours And Company | Modular system for coating plastics |
| US6995208B2 (en) | 2001-12-11 | 2006-02-07 | Basf Corporation | Clearcoat composition for primerless MVSS adhesion |
| FR2834992B1 (fr) | 2002-01-21 | 2005-05-27 | Oreal | Polymeres associatifs cationiques amphiphiles, procede de preparation, utilisation comme epaississant et composition les comprenant |
| ITTO20020069A1 (it) | 2002-01-24 | 2003-07-24 | Metlac Spa | Vernice per materiali plastici e metodo di verniciatura utilizzante tale vernice. |
| US20030187089A1 (en) | 2002-02-04 | 2003-10-02 | Lustre-Cal, A California Corporation | Perma-ink insert mold decoration system |
| US6649016B2 (en) | 2002-03-04 | 2003-11-18 | Dow Global Technologies Inc. | Silane functional adhesive composition and method of bonding a window to a substrate without a primer |
| JP2003336008A (ja) | 2002-05-23 | 2003-11-28 | Dainippon Ink & Chem Inc | 湿気硬化型ウレタンプライマー |
| JP3838953B2 (ja) * | 2002-08-26 | 2006-10-25 | 横浜ゴム株式会社 | プライマー組成物 |
| JP2004168957A (ja) | 2002-11-22 | 2004-06-17 | Yokohama Rubber Co Ltd:The | 1液湿気硬化型ポリウレタン組成物 |
| US8013068B2 (en) * | 2003-01-02 | 2011-09-06 | Rohm And Haas Company | Michael addition compositions |
| US6958189B2 (en) | 2003-03-31 | 2005-10-25 | Exatec, Llc | Ink for a polycarbonate substrate |
| US6852804B2 (en) | 2003-04-25 | 2005-02-08 | The University Of Akron | Star block copolymers and related synthetic methods |
| EP1477511A1 (en) * | 2003-05-15 | 2004-11-17 | DSM IP Assets B.V. | Radiation curable thiol-ene composition |
| ATE402235T1 (de) * | 2003-12-10 | 2008-08-15 | Dow Global Technologies Inc | System zum einbinden von glas in eine konstruktion |
| US7294656B2 (en) * | 2004-01-09 | 2007-11-13 | Bayer Materialscience Llc | UV curable coating composition |
| US7732041B2 (en) | 2004-08-02 | 2010-06-08 | Exatec Llc | Decorative ink for automotive plastic glazing |
| WO2006042305A1 (en) | 2004-10-08 | 2006-04-20 | Dow Global Technologies Inc. | Low volatile isocyanate monomer containing polyurethane prepolymer and adhesive system |
| US20060191625A1 (en) | 2005-02-28 | 2006-08-31 | Ferro Corporation | Method of decorating laminated glass |
| US20060198963A1 (en) | 2005-03-03 | 2006-09-07 | Dimitry Chernyshov | Process for the production of a coating layer on three-dimensional shaped substrates with radiation-curable coating compositions |
| US7781493B2 (en) | 2005-06-20 | 2010-08-24 | Dow Global Technologies Inc. | Protective coating for window glass |
| RU2415167C2 (ru) * | 2005-06-20 | 2011-03-27 | Дау Глобал Текнолоджиз Инк. | Защитное покрытие для оконных стекол |
| US7450245B2 (en) | 2005-06-29 | 2008-11-11 | Dcg Systems, Inc. | Method and apparatus for measuring high-bandwidth electrical signals using modulation in an optical probing system |
| JP5345281B2 (ja) | 2005-08-05 | 2013-11-20 | オート化学工業株式会社 | 硬化性組成物 |
| US7531242B2 (en) | 2005-09-30 | 2009-05-12 | Industrial Control Development, Inc. | Silicone-coated architectural glass |
| KR20090057133A (ko) | 2006-09-21 | 2009-06-03 | 피피지 인더스트리즈 오하이오 인코포레이티드 | 저온 습기 경화성 코팅 조성물 및 이와 관련된 방법 |
| US7868120B2 (en) | 2006-09-21 | 2011-01-11 | Ppg Industries Ohio, Inc. | Low temperature, moisture curable coating compositions and related methods |
| US20080085415A1 (en) | 2006-10-04 | 2008-04-10 | Chengtao Li | Decorated plastic glazing assembly via a film insert molding process |
| EP2142581B1 (en) * | 2007-04-24 | 2015-04-08 | Dow Global Technologies LLC | Improved primer adhesion promoters, compositions and methods |
| BRPI0823177A2 (pt) * | 2007-04-24 | 2013-09-24 | Dow Global Technologies Inc | aditivo para uma composiÇço de primer, mÉtodo para melhorar o desempenho de uma composiÇço de primer, composiÇço de primer e kit |
| KR101464017B1 (ko) | 2007-05-01 | 2014-12-08 | 엑사테크 엘.엘.씨. | 자외선 경화 인쇄 패턴을 가진 플라스틱 글레이징 패널과 상기 패널을 제조하는 방법 |
-
2008
- 2008-12-18 US US12/338,752 patent/US8147974B2/en active Active
- 2008-12-18 BR BRPI0819414 patent/BRPI0819414A2/pt not_active IP Right Cessation
- 2008-12-18 JP JP2010539823A patent/JP5571572B2/ja not_active Expired - Fee Related
- 2008-12-18 KR KR1020107015802A patent/KR101587666B1/ko not_active Expired - Fee Related
- 2008-12-18 CN CN200880121503.7A patent/CN101903483B/zh not_active Expired - Fee Related
- 2008-12-18 EP EP08861056.3A patent/EP2225339B1/en not_active Not-in-force
- 2008-12-18 WO PCT/US2008/087503 patent/WO2009079647A1/en not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| US8147974B2 (en) | 2012-04-03 |
| US20090162592A1 (en) | 2009-06-25 |
| KR101587666B1 (ko) | 2016-01-21 |
| EP2225339B1 (en) | 2016-06-29 |
| CN101903483A (zh) | 2010-12-01 |
| EP2225339A1 (en) | 2010-09-08 |
| JP2011506755A (ja) | 2011-03-03 |
| WO2009079647A1 (en) | 2009-06-25 |
| KR20100103828A (ko) | 2010-09-28 |
| JP5571572B2 (ja) | 2014-08-13 |
| BRPI0819414A2 (pt) | 2015-05-05 |
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