KR20060022678A - 피복된 광섬유 및 광섬유 피복에 적합한 경화성 조성물 - Google Patents
피복된 광섬유 및 광섬유 피복에 적합한 경화성 조성물 Download PDFInfo
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- KR20060022678A KR20060022678A KR1020057023367A KR20057023367A KR20060022678A KR 20060022678 A KR20060022678 A KR 20060022678A KR 1020057023367 A KR1020057023367 A KR 1020057023367A KR 20057023367 A KR20057023367 A KR 20057023367A KR 20060022678 A KR20060022678 A KR 20060022678A
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- South Korea
- Prior art keywords
- ooc
- oligomer
- coo
- optical fiber
- photomer
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Images
Classifications
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- G02B6/02—Optical fibres with cladding with or without a coating
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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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
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- 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
- C03C25/00—Surface treatment of fibres or filaments made from glass, minerals or slags
- C03C25/10—Coating
- C03C25/104—Coating to obtain optical fibres
- C03C25/106—Single coatings
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- 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
- C03C25/00—Surface treatment of fibres or filaments made from glass, minerals or slags
- C03C25/10—Coating
- C03C25/104—Coating to obtain optical fibres
- C03C25/1065—Multiple coatings
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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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- 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
- C08G18/67—Unsaturated compounds having active hydrogen
- 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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having 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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- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
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- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B6/00—Light guides; Structural details of arrangements comprising light guides and other optical elements, e.g. couplings
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
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- Macromonomer-Based Addition Polymer (AREA)
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10/454,984 US6862392B2 (en) | 2003-06-04 | 2003-06-04 | Coated optical fiber and curable compositions suitable for coating optical fiber |
| US10/454,984 | 2003-06-04 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR20060022678A true KR20060022678A (ko) | 2006-03-10 |
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Family Applications (1)
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| KR1020057023367A Withdrawn KR20060022678A (ko) | 2003-06-04 | 2004-05-20 | 피복된 광섬유 및 광섬유 피복에 적합한 경화성 조성물 |
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| Country | Link |
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| US (2) | US6862392B2 (https=) |
| EP (1) | EP1628928A2 (https=) |
| JP (1) | JP4931582B2 (https=) |
| KR (1) | KR20060022678A (https=) |
| WO (1) | WO2004108620A2 (https=) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR101957317B1 (ko) * | 2018-06-04 | 2019-03-12 | 홍수동 | 내충격성이 우수한 광섬유 코팅 조성물 및 이를 적용한 광섬유 |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| WO2004044012A1 (en) * | 2002-11-12 | 2004-05-27 | The Polymer Technology Group Incorporated | Control of polymer surface molecular architecture via amphipathic endgroups |
| US7207732B2 (en) * | 2003-06-04 | 2007-04-24 | Corning Incorporated | Coated optical fiber and curable compositions suitable for coating optical fiber |
| US6862392B2 (en) * | 2003-06-04 | 2005-03-01 | Corning Incorporated | Coated optical fiber and curable compositions suitable for coating optical fiber |
| US7715675B2 (en) * | 2003-07-18 | 2010-05-11 | Corning Incorporated | Optical fiber coating system and coated optical fiber |
| WO2005035461A1 (en) * | 2003-10-17 | 2005-04-21 | Dsm Ip Assets B.V. | Flame retardant uv cured buffered optical fibers and buffer composition |
| US7239785B2 (en) * | 2004-12-30 | 2007-07-03 | Corning Incorporated | Method of preventing optical fiber failure in high power application |
| US7295737B2 (en) * | 2005-08-04 | 2007-11-13 | Corning Cable Systems Llc | Mechanically strippable upcoated optical fiber |
| US8093322B2 (en) * | 2005-10-27 | 2012-01-10 | Corning Incorporated | Non-reactive additives for fiber coatings |
| US7470755B2 (en) * | 2005-11-29 | 2008-12-30 | Prc-Desoto International, Inc. | Polyepoxide, amine and mercaptan-terminated polyoxyalkylene |
| US7257299B2 (en) * | 2005-11-30 | 2007-08-14 | Corning Incorporated | Optical fiber ribbon with improved stripability |
| US7289706B2 (en) * | 2005-11-30 | 2007-10-30 | Corning Incorporated | Optical fiber ribbon with improved stripability |
| KR101166602B1 (ko) * | 2006-06-14 | 2012-07-18 | 히다치 가세고교 가부시끼가이샤 | 수지 조성물, 및 이것을 이용하여 이루어지는 적층형 광학부재 |
| EP2089333B1 (en) * | 2006-12-14 | 2011-02-16 | DSM IP Assets B.V. | D1363 bt radiation curable primary coatings on optical fiber |
| RU2434914C2 (ru) * | 2006-12-14 | 2011-11-27 | ДСМ Ай Пи ЭССЕТС Б.В. | Отверждаемое излучением первичное покрытие d 1368 cr для оптического волокна |
| WO2008076298A1 (en) | 2006-12-14 | 2008-06-26 | Dsm Ip Assets B.V. | D1381 supercoatings for optical fiber |
| WO2008076303A1 (en) * | 2006-12-14 | 2008-06-26 | Dsm Ip Assets B.V. | D1365 bj radiation curable primary coating for optical fiber |
| CN101535200B (zh) | 2006-12-14 | 2011-10-26 | 帝斯曼知识产权资产管理有限公司 | 光纤上的d1364bt次级涂层 |
| EP2091883B1 (en) | 2006-12-14 | 2011-02-16 | DSM IP Assets B.V. | D1364 bt secondary coating on optical fiber |
| US20080226915A1 (en) * | 2006-12-14 | 2008-09-18 | Xiaosong Wu | D1379 p radiation curable primary coating on optical fiber |
| ATE498594T1 (de) * | 2006-12-14 | 2011-03-15 | Dsm Ip Assets Bv | Strahlungshärtbare d1378 ca-grundierbeschichtung für optische fasern |
| CN101535201B (zh) * | 2006-12-14 | 2012-06-27 | 帝斯曼知识产权资产管理有限公司 | 光纤用d1370r可辐射固化次级涂层 |
| EP2131360A4 (en) * | 2007-03-23 | 2011-06-22 | Dainippon Ink & Chemicals | ULTRAVIOLETT CURABLE COMPOSITION FOR AN INTERMEDIATE LAYER FOR OPTICAL DATA CARRIER AND OPTICAL DATA CARRIER |
| KR101001656B1 (ko) * | 2008-08-26 | 2010-12-15 | 에스에스씨피 주식회사 | 광중합형 수지 조성물 및 이를 사용하여 제조되는 광섬유 |
| US20120128313A1 (en) | 2009-10-09 | 2012-05-24 | Xiaosong Wu | Radiation curable coating for optical fiber |
| KR101580424B1 (ko) | 2010-06-30 | 2015-12-24 | 디에스엠 아이피 어셋츠 비.브이. | D1479 안정한 액체 비스(아실)포스핀 광 개시제 및 방사선 경화성 조성물에서 이의 용도 |
| CN102471150B (zh) | 2010-06-30 | 2014-05-07 | 帝斯曼知识产权资产管理有限公司 | D1492液体双酰基氧化膦光引发剂及其在可辐射固化组合物中的用途 |
| US20130011108A1 (en) * | 2011-07-06 | 2013-01-10 | Ofs Fitel, Llc | UV Curable Acrylate Buffer Coating for Optical Fiber |
| US9244221B1 (en) | 2013-12-10 | 2016-01-26 | Corning Incorporated | Low modulus primary coatings for optical fibers |
| WO2016080829A1 (en) * | 2014-11-19 | 2016-05-26 | Dsm Ip Assets B.V. | D1563 radiation curable secondary coating for optical fibers |
| CN105353485A (zh) * | 2015-12-16 | 2016-02-24 | 南京华信藤仓光通信有限公司 | 防水光纤及其制备方法 |
| GB201706657D0 (en) * | 2017-04-26 | 2017-06-07 | Univ Liverpool | Polymers |
| GB201706658D0 (en) | 2017-04-26 | 2017-06-07 | Univ Liverpool | Branched Polymers |
| CN108761631B (zh) * | 2018-05-03 | 2020-06-23 | 烽火通信科技股份有限公司 | 一种掺镱光纤及其制造方法 |
| GB201817837D0 (en) | 2018-10-31 | 2018-12-19 | Univ Liverpool | Branched polymers |
| KR102847956B1 (ko) * | 2019-01-11 | 2025-08-19 | 올넥스 벨지움 에스.에이. | 경화성 수지 조성물 |
| US11822117B2 (en) * | 2019-10-08 | 2023-11-21 | Corning Incorporated | Primary coating compositions with improved microbending performance |
| US11371943B2 (en) | 2020-10-01 | 2022-06-28 | Consolidated Nuclear Security, LLC | Coated fiber optic chemical and radiation sensors |
| US11513078B2 (en) | 2020-10-01 | 2022-11-29 | Consolidated Nuclear Security, LLC | Coated fiber optic chemical and radiation sensors |
Family Cites Families (64)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4390565A (en) | 1982-08-26 | 1983-06-28 | Lord Corporation | Photocurable compositions for use as ceramic ink vehicles |
| US4514037A (en) | 1983-10-21 | 1985-04-30 | Desoto, Inc. | Ultraviolet curable outer coatings for optical fiber |
| US4608409A (en) | 1985-05-08 | 1986-08-26 | Desoto, Inc. | Polyacrylated oligomers in ultraviolet curable optical fiber coatings |
| JPS6474514A (en) * | 1987-09-17 | 1989-03-20 | Sumitomo Electric Industries | Optical fiber cable |
| US4889901A (en) | 1988-11-16 | 1989-12-26 | Desoto, Inc. | Ultraviolet-curable blends of acrylated polyurethanes and silsesquioxane oligomers having improved adhesion to glass |
| US5536529A (en) | 1989-05-11 | 1996-07-16 | Borden, Inc. | Ultraviolet radiation-curable coatings for optical fibers and optical fibers coated therewith |
| US4962992A (en) | 1989-05-15 | 1990-10-16 | At&T Bell Laboratories | Optical transmission media and methods of making same |
| US5093386A (en) | 1989-05-16 | 1992-03-03 | Stamicarbon B.V. | Liquid curable plastic composition |
| US5140665A (en) * | 1989-12-22 | 1992-08-18 | Corning Incorporated | Optical waveguide fiber with titania-silica outer cladding |
| GB9121655D0 (en) * | 1991-10-11 | 1991-11-27 | Ici Plc | Optical fibre coating |
| CA2082614A1 (en) * | 1992-04-24 | 1993-10-25 | Paul J. Shustack | Organic solvent and water resistant, thermally, oxidatively and hydrolytically stable radiation-curable coatings for optical fibers, optical fibers coated therewith and processes for making same |
| JPH05323160A (ja) * | 1992-05-20 | 1993-12-07 | Sumitomo Electric Ind Ltd | 光伝送用ガラスファイバ |
| US5259060A (en) * | 1992-08-11 | 1993-11-02 | Corning Incorporated | Coated optical fibers and method |
| JP3460727B2 (ja) * | 1992-08-12 | 2003-10-27 | 日本電信電話株式会社 | 酸素イオン導伝体及び固体燃料電池 |
| WO1995021800A1 (fr) * | 1994-02-15 | 1995-08-17 | Sumitomo Electric Industries, Ltd. | Fibre optique revetue et son procede de production |
| US6472450B2 (en) | 1995-03-13 | 2002-10-29 | Dsm N.V. | Radiation-curable optical fiber coating composition |
| DE69608671T2 (de) | 1995-03-13 | 2001-02-15 | Dsm N.V., Heerlen | Optische glasfaser beschichtet mit einer strahlungshärtbaren beschichtungszusammensetzung |
| AU705014B2 (en) | 1995-08-01 | 1999-05-13 | Dsm N.V. | A ribbon unit, a method of making the ribbon unit and a method of providing mid-span access |
| US5578693A (en) | 1995-09-05 | 1996-11-26 | Bomar Specialties Company | Multifunctional terminally unsaturated urethane oligomers |
| US5744514A (en) | 1996-10-31 | 1998-04-28 | Borden Chemical, Inc. | Coated optical fibers having a reduced content of extractable and volatile material |
| JP3955333B2 (ja) | 1996-11-08 | 2007-08-08 | デーエスエム アイピー アセッツ ベー．ヴェー． | 放射線硬化性の光ガラスファイバー被覆用組成物、被覆光ガラスファイバー、及び光ガラスファイバーアセンブリー |
| EP0894277A4 (en) | 1997-01-24 | 2002-07-31 | Borden Chem Inc | COATED OPTICAL FIBERS WITH REMOVABLE PRIMARY COATINGS AND MANUFACTURING METHOD AND USE |
| CN1259146A (zh) | 1997-04-08 | 2000-07-05 | Dsm有限公司 | 固化后具有高伸长和韧性的可辐射硬化的粘合剂组合物 |
| KR100593519B1 (ko) | 1997-04-22 | 2006-06-28 | 코닌클리즈케 디에스엠 엔.브이. | 액상 경화성 수지 조성물 |
| JPH1111986A (ja) | 1997-04-25 | 1999-01-19 | Takeda Chem Ind Ltd | 光ファイバ被覆用樹脂組成物 |
| JPH1160991A (ja) | 1997-08-22 | 1999-03-05 | Jsr Corp | 液状硬化性樹脂組成物 |
| JPH11116282A (ja) * | 1997-10-06 | 1999-04-27 | Sumitomo Electric Ind Ltd | 被覆光ファイバ |
| DE19746658A1 (de) * | 1997-10-22 | 1999-04-29 | Emitec Emissionstechnologie | Verfahren und Vorrichtung zur Regelung des Temperaturbereiches eines NOx-Speichers in einer Abgasanlage eines Verbrennungsmotors |
| JPH11131019A (ja) * | 1997-10-27 | 1999-05-18 | Kansai Paint Co Ltd | 光ファイバー用紫外線硬化型樹脂組成物 |
| US6110593A (en) | 1998-05-21 | 2000-08-29 | Dsm N.V. | Radiation-curable optical fiber primary coating system |
| US6215934B1 (en) | 1998-10-01 | 2001-04-10 | Lucent Technologies, Inc. | Coated optical fiber with improved strippability |
| US5908484A (en) | 1998-10-16 | 1999-06-01 | Lucent Technologies Inc. | Method of making a coated optical fiber comprising measuring the delamination resistance of the coating |
| US6243523B1 (en) | 1999-06-29 | 2001-06-05 | Lucent Technologies Inc. | Coated optical fiber with increased modulus and thermally enhanced strippability |
| EP1254082A1 (en) | 1999-12-30 | 2002-11-06 | Corning Incorporated | Fast curing primary optical fiber coating |
| WO2001049625A1 (en) | 1999-12-30 | 2001-07-12 | Corning Incorporated | Optical fibers prepared with a primary coating composition including a monomer with a pendant hydroxyl functional group |
| DE60032944T2 (de) | 1999-12-30 | 2007-10-18 | Corning Inc. | Sekundärbeschichtung für lichtleitfasern |
| EP1250386A1 (en) | 1999-12-30 | 2002-10-23 | Corning Incorporated | Composition containing tackifier and method of modifying time-sensitive rheological properties of optical fiber coating |
| AU2001271237A1 (en) | 2000-05-01 | 2001-11-12 | Corning Incorporated | Optical fiber coating |
| US6579914B1 (en) | 2000-07-14 | 2003-06-17 | Alcatel | Coating compositions for optical waveguides and optical waveguides coated therewith |
| US6584263B2 (en) | 2000-07-26 | 2003-06-24 | Corning Incorporated | Optical fiber coating compositions and coated optical fibers |
| CN1230944C (zh) * | 2000-08-09 | 2005-12-07 | Jsr株式会社 | 各向异性导电板 |
| JP2002097235A (ja) | 2000-09-26 | 2002-04-02 | Jsr Corp | 液状硬化性樹脂組成物およびその硬化物 |
| US20030215196A1 (en) * | 2000-11-22 | 2003-11-20 | Dsm N.V. | Coated optical fibers |
| US7067564B2 (en) | 2000-11-22 | 2006-06-27 | Dsm Ip Assets B.V. | Coated optical fibers |
| US6553169B2 (en) | 2000-11-29 | 2003-04-22 | Corning Incorporated | Optical fiber coating compositions and coated optical fibers |
| US6611647B2 (en) * | 2000-12-12 | 2003-08-26 | Corning Incorporated | Large effective area optical fiber |
| EP1370499A2 (en) | 2000-12-29 | 2003-12-17 | DSM IP Assets B.V. | Non-crystal-forming oligomers for use in radiation-curable fiber optic coatings |
| US7226958B2 (en) | 2001-01-12 | 2007-06-05 | Dsm Ip Assets B.V. | Urethane-acrylic coatings for optical fiber |
| US20030077059A1 (en) | 2001-03-13 | 2003-04-24 | Ching-Kee Chien | Optical fiber coating compositions |
| US6596394B2 (en) | 2001-03-14 | 2003-07-22 | Corning Incorporated | Coated optical fiber |
| US6707977B2 (en) * | 2001-03-15 | 2004-03-16 | Corning Incorporated | All fiber polarization mode dispersion compensator |
| US7118780B2 (en) * | 2001-03-16 | 2006-10-10 | Semiconductor Energy Laboratory Co., Ltd. | Heat treatment method |
| US6849333B2 (en) | 2001-05-18 | 2005-02-01 | Corning Incorporated | Optical fiber with an improved primary coating composition |
| US6628875B2 (en) | 2001-07-20 | 2003-09-30 | Corning Incorporated | Optical fibers possessing a primary coating with a higher degree of cure and methods of making |
| US20030123839A1 (en) | 2001-07-27 | 2003-07-03 | Chou Kevin Y. | Low modulus, high tensile strength optical fiber coating |
| US6869981B2 (en) | 2001-09-21 | 2005-03-22 | Corning Incorporated | Optical fiber coatings with pressure sensitive adhesive characteristics |
| JP2003104760A (ja) * | 2001-09-28 | 2003-04-09 | Sumitomo Electric Ind Ltd | 被覆光ファイバおよびこれを用いた光ファイバ心線 |
| US6689463B2 (en) * | 2001-12-18 | 2004-02-10 | Corning Incorporated | Secondary coating composition for optical fibers |
| US7105583B2 (en) | 2001-12-20 | 2006-09-12 | Ppg Industries Ohio, Inc. | Radiation-curable compositions for optical fiber coating materials |
| US20030119998A1 (en) | 2001-12-20 | 2003-06-26 | Shengkui Hu | Free radical-curable composition for optical fiber coating materials |
| US6862392B2 (en) | 2003-06-04 | 2005-03-01 | Corning Incorporated | Coated optical fiber and curable compositions suitable for coating optical fiber |
| US7715675B2 (en) * | 2003-07-18 | 2010-05-11 | Corning Incorporated | Optical fiber coating system and coated optical fiber |
| US7050688B2 (en) * | 2003-07-18 | 2006-05-23 | Corning Cable Systems Llc | Fiber optic articles, assemblies, and cables having optical waveguides |
| US7423105B2 (en) * | 2005-09-30 | 2008-09-09 | Corning Incorporated | Fast curing primary optical fiber coatings |
-
2003
- 2003-06-04 US US10/454,984 patent/US6862392B2/en not_active Ceased
-
2004
- 2004-05-20 JP JP2006514925A patent/JP4931582B2/ja not_active Expired - Fee Related
- 2004-05-20 WO PCT/US2004/016105 patent/WO2004108620A2/en not_active Ceased
- 2004-05-20 KR KR1020057023367A patent/KR20060022678A/ko not_active Withdrawn
- 2004-05-20 EP EP04753005A patent/EP1628928A2/en not_active Withdrawn
-
2007
- 2007-02-23 US US11/710,229 patent/USRE43480E1/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR101957317B1 (ko) * | 2018-06-04 | 2019-03-12 | 홍수동 | 내충격성이 우수한 광섬유 코팅 조성물 및 이를 적용한 광섬유 |
Also Published As
| Publication number | Publication date |
|---|---|
| US6862392B2 (en) | 2005-03-01 |
| JP2006526563A (ja) | 2006-11-24 |
| WO2004108620A2 (en) | 2004-12-16 |
| WO2004108620A3 (en) | 2005-02-17 |
| JP4931582B2 (ja) | 2012-05-16 |
| US20040247273A1 (en) | 2004-12-09 |
| USRE43480E1 (en) | 2012-06-19 |
| EP1628928A2 (en) | 2006-03-01 |
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