KR100961426B1 - 중합체 필름을 포함하는 광학 보상 시트 - Google Patents
중합체 필름을 포함하는 광학 보상 시트 Download PDFInfo
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- KR100961426B1 KR100961426B1 KR1020047016839A KR20047016839A KR100961426B1 KR 100961426 B1 KR100961426 B1 KR 100961426B1 KR 1020047016839 A KR1020047016839 A KR 1020047016839A KR 20047016839 A KR20047016839 A KR 20047016839A KR 100961426 B1 KR100961426 B1 KR 100961426B1
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- 125000000842 isoxazolyl group Chemical group 0.000 description 1
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- 239000002346 layers by function Substances 0.000 description 1
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- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- GYNNXHKOJHMOHS-UHFFFAOYSA-N methyl-cycloheptane Natural products CC1CCCCCC1 GYNNXHKOJHMOHS-UHFFFAOYSA-N 0.000 description 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
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- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 description 1
- WIBFFTLQMKKBLZ-SEYXRHQNSA-N n-butyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCCCC WIBFFTLQMKKBLZ-SEYXRHQNSA-N 0.000 description 1
- IZXDTJXEUISVAJ-UHFFFAOYSA-N n-methyl-n-octadecyloctadecan-1-amine;hydrochloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[NH+](C)CCCCCCCCCCCCCCCCCC IZXDTJXEUISVAJ-UHFFFAOYSA-N 0.000 description 1
- KVBGVZZKJNLNJU-UHFFFAOYSA-M naphthalene-2-sulfonate Chemical compound C1=CC=CC2=CC(S(=O)(=O)[O-])=CC=C21 KVBGVZZKJNLNJU-UHFFFAOYSA-M 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 229920001220 nitrocellulos Polymers 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000004866 oxadiazoles Chemical class 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- QUBQYFYWUJJAAK-UHFFFAOYSA-N oxymethurea Chemical compound OCNC(=O)NCO QUBQYFYWUJJAAK-UHFFFAOYSA-N 0.000 description 1
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- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
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- 150000002978 peroxides Chemical class 0.000 description 1
- 125000001791 phenazinyl group Chemical class C1(=CC=CC2=NC3=CC=CC=C3N=C12)* 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- 125000006678 phenoxycarbonyl group Chemical group 0.000 description 1
- OPYYWWIJPHKUDZ-UHFFFAOYSA-N phenyl cyclohexanecarboxylate Chemical group C1CCCCC1C(=O)OC1=CC=CC=C1 OPYYWWIJPHKUDZ-UHFFFAOYSA-N 0.000 description 1
- 125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
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- 239000011574 phosphorus Substances 0.000 description 1
- 239000003504 photosensitizing agent Substances 0.000 description 1
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- 229920000573 polyethylene Polymers 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920000379 polypropylene carbonate Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
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- 239000000843 powder Substances 0.000 description 1
- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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- 239000011241 protective layer Substances 0.000 description 1
- 125000004309 pyranyl group Chemical group O1C(C=CC=C1)* 0.000 description 1
- 125000003226 pyrazolyl group Chemical group 0.000 description 1
- PBMFSQRYOILNGV-UHFFFAOYSA-N pyridazine Chemical group C1=CC=NN=C1 PBMFSQRYOILNGV-UHFFFAOYSA-N 0.000 description 1
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- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 230000001953 sensory effect Effects 0.000 description 1
- UQDJGEHQDNVPGU-UHFFFAOYSA-N serine phosphoethanolamine Chemical compound [NH3+]CCOP([O-])(=O)OCC([NH3+])C([O-])=O UQDJGEHQDNVPGU-UHFFFAOYSA-N 0.000 description 1
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- 238000012360 testing method Methods 0.000 description 1
- RAOIDOHSFRTOEL-UHFFFAOYSA-N tetrahydrothiophene Chemical group C1CCSC1 RAOIDOHSFRTOEL-UHFFFAOYSA-N 0.000 description 1
- 238000012719 thermal polymerization Methods 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- WEAPVABOECTMGR-UHFFFAOYSA-N triethyl 2-acetyloxypropane-1,2,3-tricarboxylate Chemical compound CCOC(=O)CC(C(=O)OCC)(OC(C)=O)CC(=O)OCC WEAPVABOECTMGR-UHFFFAOYSA-N 0.000 description 1
- ARCGXLSVLAOJQL-UHFFFAOYSA-N trimellitic acid Chemical class OC(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 ARCGXLSVLAOJQL-UHFFFAOYSA-N 0.000 description 1
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Classifications
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B1/00—Optical elements characterised by the material of which they are made; Optical coatings for optical elements
- G02B1/04—Optical elements characterised by the material of which they are made; Optical coatings for optical elements made of organic materials, e.g. plastics
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B5/00—Optical elements other than lenses
- G02B5/30—Polarising elements
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/18—Manufacture of films or sheets
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B5/00—Optical elements other than lenses
- G02B5/20—Filters
- G02B5/208—Filters for use with infrared or ultraviolet radiation, e.g. for separating visible light from infrared and/or ultraviolet radiation
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B5/00—Optical elements other than lenses
- G02B5/30—Polarising elements
- G02B5/3083—Birefringent or phase retarding elements
-
- G—PHYSICS
- G02—OPTICS
- G02F—OPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
- G02F1/00—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
- G02F1/01—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour
- G02F1/13—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells
- G02F1/133—Constructional arrangements; Operation of liquid crystal cells; Circuit arrangements
- G02F1/1333—Constructional arrangements; Manufacturing methods
- G02F1/1335—Structural association of cells with optical devices, e.g. polarisers or reflectors
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2301/00—Characterised by the use of cellulose, modified cellulose or cellulose derivatives
- C08J2301/08—Cellulose derivatives
- C08J2301/10—Esters of organic acids
- C08J2301/12—Cellulose acetate
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2323/00—Functional layers of liquid crystal optical display excluding electroactive liquid crystal layer characterised by chemical composition
- C09K2323/03—Viewing layer characterised by chemical composition
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2323/00—Functional layers of liquid crystal optical display excluding electroactive liquid crystal layer characterised by chemical composition
- C09K2323/03—Viewing layer characterised by chemical composition
- C09K2323/035—Ester polymer, e.g. polycarbonate, polyacrylate or polyester
Landscapes
- Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- General Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Organic Chemistry (AREA)
- Polymers & Plastics (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Toxicology (AREA)
- Nonlinear Science (AREA)
- Crystallography & Structural Chemistry (AREA)
- Mathematical Physics (AREA)
- Polarising Elements (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Liquid Crystal (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JPJP-P-2002-00118199 | 2002-04-19 | ||
| JP2002118199 | 2002-04-19 | ||
| JPJP-P-2003-00027488 | 2003-02-04 | ||
| JP2003027488A JP4076454B2 (ja) | 2002-04-19 | 2003-02-04 | 光学補償シート、偏光板および画像表示装置 |
| PCT/JP2003/004998 WO2003089965A1 (en) | 2002-04-19 | 2003-04-18 | Optical compensatory sheet comprising polymer film |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR20040104568A KR20040104568A (ko) | 2004-12-10 |
| KR100961426B1 true KR100961426B1 (ko) | 2010-06-09 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020047016839A Expired - Lifetime KR100961426B1 (ko) | 2002-04-19 | 2003-04-18 | 중합체 필름을 포함하는 광학 보상 시트 |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US7105212B2 (enExample) |
| EP (1) | EP1497678A4 (enExample) |
| JP (1) | JP4076454B2 (enExample) |
| KR (1) | KR100961426B1 (enExample) |
| CN (1) | CN1306293C (enExample) |
| AU (1) | AU2003228102A1 (enExample) |
| TW (1) | TWI264568B (enExample) |
| WO (1) | WO2003089965A1 (enExample) |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2005521100A (ja) * | 2002-03-26 | 2005-07-14 | 富士写真フイルム株式会社 | 偏光板および液晶表示装置 |
| JP2005242337A (ja) * | 2004-01-26 | 2005-09-08 | Fuji Photo Film Co Ltd | ポリマーフィルムおよびポリマー溶液の調製方法 |
| CN100447594C (zh) * | 2004-03-25 | 2008-12-31 | 富士胶片株式会社 | 透明薄膜和使用它的光学补偿薄膜、偏振片和液晶显示装置 |
| US8187681B2 (en) | 2004-03-25 | 2012-05-29 | Fujifilm Corporation | Transparent film and optical compensatory film, polarizing plate and liquid-crystal display device employing it |
| JP2006293255A (ja) * | 2004-05-18 | 2006-10-26 | Fuji Photo Film Co Ltd | 光学フィルム、光学補償フィルム、偏光板、液晶表示装置、および自発光型表示装置 |
| TWI353461B (en) * | 2004-05-18 | 2011-12-01 | Fujifilm Corp | Optical film, optical compensation film, polarizin |
| JP4731143B2 (ja) * | 2004-09-17 | 2011-07-20 | 富士フイルム株式会社 | セルロースアシレートフイルム、光学補償フイルム、偏光板および液晶表示装置 |
| TWI383011B (zh) * | 2004-08-13 | 2013-01-21 | Fujifilm Corp | 醯化纖維素薄膜、光學補償膜、偏光板及液晶顯示裝置 |
| JP2006064803A (ja) * | 2004-08-25 | 2006-03-09 | Konica Minolta Opto Inc | 延伸セルロースエステルフィルム、それを用いた偏光板及び液晶表示装置 |
| JP4546196B2 (ja) * | 2004-09-22 | 2010-09-15 | 富士フイルム株式会社 | 位相差板 |
| KR20070086056A (ko) | 2004-12-15 | 2007-08-27 | 후지필름 가부시키가이샤 | 셀룰로오스 아실레이트 필름, 셀룰로오스 아실레이트필름의 제조 방법, 편광판 및 액정 표시 장치 |
| JP4619108B2 (ja) * | 2004-12-22 | 2011-01-26 | 富士フイルム株式会社 | 液晶表示装置 |
| WO2006090887A1 (en) * | 2005-02-23 | 2006-08-31 | Fujifilm Corporation | Optical compensation sheet and liquid crystal display device |
| TWI446025B (zh) * | 2005-03-17 | 2014-07-21 | Fuji Corp | 光學樹脂薄膜、光學補償片、偏光板及液晶顯示器 |
| KR101247827B1 (ko) * | 2005-03-31 | 2013-03-26 | 가부시키가이샤 가네카 | 위상차 필름 및 그의 제조 방법 |
| JP2008537158A (ja) * | 2005-04-22 | 2008-09-11 | 富士フイルム株式会社 | 光学フィルム、偏光板および液晶表示装置 |
| JP2006342226A (ja) * | 2005-06-08 | 2006-12-21 | Konica Minolta Opto Inc | セルロースエステルフィルム、及びそれを用いた偏光板、表示装置 |
| CN100580487C (zh) * | 2005-07-21 | 2010-01-13 | 柯尼卡美能达精密光学株式会社 | 亲水性聚合物膜的制造方法 |
| TWI421597B (zh) | 2005-08-22 | 2014-01-01 | Fujifilm Corp | 光學膜、光學補償膜、與使用它之偏光板及液晶顯示器 |
| KR20080023751A (ko) * | 2005-08-23 | 2008-03-14 | 닛토덴코 가부시키가이샤 | 액정 패널 및 그것을 이용한 액정 표시 장치 |
| JP5181673B2 (ja) * | 2005-08-30 | 2013-04-10 | コニカミノルタアドバンストレイヤー株式会社 | 液晶表示装置 |
| US7630038B2 (en) * | 2005-11-10 | 2009-12-08 | Nitto Denko Cororation | Liquid crystal panel and liquid crystal display apparatus |
| JP2007178984A (ja) | 2005-11-29 | 2007-07-12 | Nitto Denko Corp | 液晶パネルおよび液晶表示装置 |
| JP5093106B2 (ja) | 2006-04-26 | 2012-12-05 | コニカミノルタアドバンストレイヤー株式会社 | 偏光板用光学補償樹脂フィルム、光学補償樹脂フィルムの製造方法、偏光板及び液晶表示装置 |
| KR101486077B1 (ko) * | 2006-08-18 | 2015-01-23 | 후지필름 가부시키가이샤 | 광학 보상 필름, 편광판 및 액정 표시 장치 |
| JP4744398B2 (ja) * | 2006-08-25 | 2011-08-10 | 富士フイルム株式会社 | 光学補償フィルム、偏光板及び液晶表示装置 |
| US20080158488A1 (en) * | 2006-12-21 | 2008-07-03 | Fujifilm Corporation | Liquid Crystal Display Device |
| US20090096962A1 (en) * | 2007-05-14 | 2009-04-16 | Eastman Chemical Company | Cellulose Esters with High Hyrdoxyl Content and Their Use in Liquid Crystal Displays |
| EP2179311B1 (en) | 2007-08-14 | 2015-09-16 | LG Chem, Ltd. | Optical film and method of manufacturing the same |
| JP2010020269A (ja) * | 2007-09-28 | 2010-01-28 | Fujifilm Corp | 液晶表示装置 |
| EP2075601A1 (de) * | 2007-12-24 | 2009-07-01 | Lofo High Tech Film GmbH | Optische Kompensationsfolien für Flüssigkristallanzeigen und damit zusammenhängende Erfindungen |
| US20110051050A1 (en) * | 2008-01-18 | 2011-03-03 | Lg Chem, Ltd. | Optical film, preparation method of the same, and liquid crystal display comprising the same |
| JP2011186358A (ja) * | 2010-03-11 | 2011-09-22 | Fujifilm Corp | ポリマーフィルム、その製造方法、それを用いた位相差フィルム、偏光板及び液晶表示装置 |
| US20110319531A1 (en) | 2010-06-29 | 2011-12-29 | Eastman Chemical Company | Cellulose ester compositions |
| US9273195B2 (en) | 2010-06-29 | 2016-03-01 | Eastman Chemical Company | Tires comprising cellulose ester/elastomer compositions |
| JP2013083953A (ja) * | 2011-09-30 | 2013-05-09 | Fujifilm Corp | 光学積層フィルム、並びにそれを用いた偏光板及び液晶表示装置 |
| US9708474B2 (en) | 2011-12-07 | 2017-07-18 | Eastman Chemical Company | Cellulose esters in pneumatic tires |
| US10077342B2 (en) | 2016-01-21 | 2018-09-18 | Eastman Chemical Company | Elastomeric compositions comprising cellulose ester additives |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2000111914A (ja) | 1998-09-30 | 2000-04-21 | Fuji Photo Film Co Ltd | セルロースの低級脂肪酸エステルフイルム用レターデーション上昇剤、光学補償シートおよび液晶表示装置 |
| JP2002071954A (ja) | 2000-09-05 | 2002-03-12 | Fuji Photo Film Co Ltd | 光学補償シート、偏光板および液晶表示装置 |
| JP2002098835A (ja) | 2000-09-25 | 2002-04-05 | Fuji Photo Film Co Ltd | 光学補償シート、偏光板および液晶表示装置 |
Family Cites Families (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6415851A (en) * | 1987-07-10 | 1989-01-19 | Nec Corp | Recognizing system for input/output device name |
| US5298575A (en) * | 1992-11-30 | 1994-03-29 | The Dow Chemical Company | Nitro group terminated mesogenic epoxy resin adducts |
| JPH09203890A (ja) * | 1996-01-25 | 1997-08-05 | Sharp Corp | 入力機能付き液晶表示素子および反射型入力機能付き液晶表示素子、並びにそれらの製造方法 |
| TW412656B (en) * | 1996-04-26 | 2000-11-21 | Hitachi Ltd | Liquid crystal display |
| JP3854392B2 (ja) * | 1996-11-11 | 2006-12-06 | 同和鉱業株式会社 | 光学的フィルター |
| JP4006608B2 (ja) | 1997-09-05 | 2007-11-14 | 大日本インキ化学工業株式会社 | 液晶性（メタ）アクリレート化合物、該化合物を含有する組成物及びこれを用いた光学異方体 |
| JP2000112663A (ja) | 1997-11-27 | 2000-04-21 | Kanegafuchi Chem Ind Co Ltd | 透明タッチパネルおよび透明タッチパネル付液晶セル |
| JP2000056301A (ja) | 1998-08-04 | 2000-02-25 | Kanegafuchi Chem Ind Co Ltd | 光学装置 |
| JP4303333B2 (ja) | 1998-08-21 | 2009-07-29 | 新日本石油株式会社 | 光学素子用フィルム |
| DE19941567A1 (de) | 1998-09-05 | 2000-04-20 | Merck Patent Gmbh | Neue flüssigkristalline Verbindungen |
| JP3459779B2 (ja) | 1998-10-30 | 2003-10-27 | 帝人株式会社 | 位相差板 |
| JP4094792B2 (ja) | 1999-02-17 | 2008-06-04 | 富士フイルム株式会社 | 光学補償シート、楕円偏光板および液晶表示装置 |
| EP1182470A4 (en) * | 1999-04-21 | 2007-04-25 | Fujifilm Corp | PHASE CONTRAST PLATE COMPRISING A CELLULOSE ESTER FILM SHEET CONTAINING AN AROMATIC COMPOUND |
| JP2001098086A (ja) | 1999-09-29 | 2001-04-10 | Fuji Photo Film Co Ltd | セルロースエステルフイルムの製造方法およびセルロースエステルフイルムの複屈折率上昇方法 |
| JP2001154194A (ja) | 1999-11-25 | 2001-06-08 | Konica Corp | 光学補償シートおよびそれを用いた液晶表示装置 |
| JP2001154018A (ja) | 1999-11-25 | 2001-06-08 | Konica Corp | 光学補償シートおよびそれを用いた液晶表示装置 |
| JP2001208913A (ja) * | 2000-01-27 | 2001-08-03 | Fuji Photo Film Co Ltd | 位相差板および円偏光板 |
| JP2002099388A (ja) | 2000-07-19 | 2002-04-05 | Fuji Photo Film Co Ltd | タッチパネル、反射型液晶表示装置およびゲストホスト型液晶表示装置 |
| JP4219538B2 (ja) * | 2000-07-19 | 2009-02-04 | 富士フイルム株式会社 | 光学補償シートの製造方法 |
| US6844033B2 (en) * | 2001-03-01 | 2005-01-18 | Konica Corporation | Cellulose ester film, its manufacturing method, polarizing plate, and liquid crystal display |
| JP3896404B2 (ja) * | 2001-03-14 | 2007-03-22 | 富士フイルム株式会社 | セルロースエステルフイルム用添加剤およびセルロースエステルフイルム |
-
2003
- 2003-02-04 JP JP2003027488A patent/JP4076454B2/ja not_active Expired - Lifetime
- 2003-04-18 EP EP03725612A patent/EP1497678A4/en not_active Withdrawn
- 2003-04-18 TW TW092109111A patent/TWI264568B/zh not_active IP Right Cessation
- 2003-04-18 US US10/508,864 patent/US7105212B2/en not_active Expired - Lifetime
- 2003-04-18 WO PCT/JP2003/004998 patent/WO2003089965A1/en not_active Ceased
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- 2003-04-18 KR KR1020047016839A patent/KR100961426B1/ko not_active Expired - Lifetime
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2000111914A (ja) | 1998-09-30 | 2000-04-21 | Fuji Photo Film Co Ltd | セルロースの低級脂肪酸エステルフイルム用レターデーション上昇剤、光学補償シートおよび液晶表示装置 |
| JP2002071954A (ja) | 2000-09-05 | 2002-03-12 | Fuji Photo Film Co Ltd | 光学補償シート、偏光板および液晶表示装置 |
| JP2002098835A (ja) | 2000-09-25 | 2002-04-05 | Fuji Photo Film Co Ltd | 光学補償シート、偏光板および液晶表示装置 |
Also Published As
| Publication number | Publication date |
|---|---|
| CN1646954A (zh) | 2005-07-27 |
| AU2003228102A1 (en) | 2003-11-03 |
| EP1497678A1 (en) | 2005-01-19 |
| TW200403453A (en) | 2004-03-01 |
| US7105212B2 (en) | 2006-09-12 |
| TWI264568B (en) | 2006-10-21 |
| JP2004004550A (ja) | 2004-01-08 |
| KR20040104568A (ko) | 2004-12-10 |
| CN1306293C (zh) | 2007-03-21 |
| WO2003089965A1 (en) | 2003-10-30 |
| JP4076454B2 (ja) | 2008-04-16 |
| US20050123693A1 (en) | 2005-06-09 |
| EP1497678A4 (en) | 2011-12-14 |
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