JP2005527847A - K型偏光子およびその製造 - Google Patents
K型偏光子およびその製造 Download PDFInfo
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- JP2005527847A JP2005527847A JP2003582560A JP2003582560A JP2005527847A JP 2005527847 A JP2005527847 A JP 2005527847A JP 2003582560 A JP2003582560 A JP 2003582560A JP 2003582560 A JP2003582560 A JP 2003582560A JP 2005527847 A JP2005527847 A JP 2005527847A
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- Prior art keywords
- vinyl alcohol
- polymer
- layer
- poly
- alcohol polymer
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- 238000004519 manufacturing process Methods 0.000 title claims abstract description 12
- 229920002451 polyvinyl alcohol Polymers 0.000 claims abstract description 223
- 239000002253 acid Substances 0.000 claims abstract description 146
- 238000000034 method Methods 0.000 claims abstract description 70
- 238000006297 dehydration reaction Methods 0.000 claims abstract description 46
- 230000018044 dehydration Effects 0.000 claims abstract description 45
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 claims abstract description 35
- 229920001577 copolymer Polymers 0.000 claims abstract description 34
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 claims abstract description 26
- 239000010410 layer Substances 0.000 claims description 264
- 229920000642 polymer Polymers 0.000 claims description 105
- -1 vinyl halide Chemical class 0.000 claims description 46
- 238000000576 coating method Methods 0.000 claims description 41
- 239000011248 coating agent Substances 0.000 claims description 38
- 230000004888 barrier function Effects 0.000 claims description 36
- 238000010438 heat treatment Methods 0.000 claims description 32
- 239000000203 mixture Substances 0.000 claims description 24
- 229920002554 vinyl polymer Polymers 0.000 claims description 23
- 239000011159 matrix material Substances 0.000 claims description 21
- 125000003118 aryl group Chemical group 0.000 claims description 19
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims description 15
- 239000000853 adhesive Substances 0.000 claims description 15
- 230000001070 adhesive effect Effects 0.000 claims description 14
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 13
- 230000004913 activation Effects 0.000 claims description 11
- 239000012790 adhesive layer Substances 0.000 claims description 11
- 125000000217 alkyl group Chemical group 0.000 claims description 11
- 238000009792 diffusion process Methods 0.000 claims description 11
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 claims description 10
- 239000000178 monomer Substances 0.000 claims description 10
- 229920001519 homopolymer Polymers 0.000 claims description 8
- 239000003795 chemical substances by application Substances 0.000 claims description 7
- 150000001875 compounds Chemical class 0.000 claims description 6
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- 125000000524 functional group Chemical group 0.000 claims description 4
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- 125000004209 (C1-C8) alkyl group Chemical group 0.000 claims description 3
- 239000007848 Bronsted acid Substances 0.000 claims description 3
- 239000002841 Lewis acid Substances 0.000 claims description 3
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- 238000005266 casting Methods 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 229920001600 hydrophobic polymer Polymers 0.000 claims description 3
- 150000007517 lewis acids Chemical class 0.000 claims description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
- 229920000573 polyethylene Polymers 0.000 claims description 3
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 2
- 239000005977 Ethylene Substances 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- 229920006254 polymer film Polymers 0.000 claims description 2
- 150000007519 polyprotic acids Polymers 0.000 claims description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims 1
- 238000010030 laminating Methods 0.000 claims 1
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 abstract description 14
- 239000004372 Polyvinyl alcohol Substances 0.000 description 21
- 239000004800 polyvinyl chloride Substances 0.000 description 21
- 229920000915 polyvinyl chloride Polymers 0.000 description 20
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 18
- 238000006243 chemical reaction Methods 0.000 description 16
- 230000003287 optical effect Effects 0.000 description 16
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- 125000004432 carbon atom Chemical group C* 0.000 description 15
- 241000238557 Decapoda Species 0.000 description 14
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- DXPPIEDUBFUSEZ-UHFFFAOYSA-N 6-methylheptyl prop-2-enoate Chemical compound CC(C)CCCCCOC(=O)C=C DXPPIEDUBFUSEZ-UHFFFAOYSA-N 0.000 description 12
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- MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 description 10
- 125000001072 heteroaryl group Chemical group 0.000 description 10
- 229920001197 polyacetylene Polymers 0.000 description 10
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical group C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 9
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- 230000007062 hydrolysis Effects 0.000 description 9
- 238000006460 hydrolysis reaction Methods 0.000 description 9
- 239000000463 material Substances 0.000 description 9
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 8
- MGNCLNQXLYJVJD-UHFFFAOYSA-N cyanuric chloride Chemical compound ClC1=NC(Cl)=NC(Cl)=N1 MGNCLNQXLYJVJD-UHFFFAOYSA-N 0.000 description 8
- 239000006185 dispersion Substances 0.000 description 8
- 125000005678 ethenylene group Chemical group [H]C([*:1])=C([H])[*:2] 0.000 description 8
- 238000006116 polymerization reaction Methods 0.000 description 8
- 239000006188 syrup Substances 0.000 description 8
- 235000020357 syrup Nutrition 0.000 description 8
- 229920001296 polysiloxane Polymers 0.000 description 7
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- 125000001424 substituent group Chemical group 0.000 description 6
- 239000000758 substrate Substances 0.000 description 6
- 239000005968 1-Decanol Substances 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 5
- 150000007513 acids Chemical class 0.000 description 5
- 230000005540 biological transmission Effects 0.000 description 5
- 150000002148 esters Chemical class 0.000 description 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 5
- PSGCQDPCAWOCSH-UHFFFAOYSA-N (4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl) prop-2-enoate Chemical compound C1CC2(C)C(OC(=O)C=C)CC1C2(C)C PSGCQDPCAWOCSH-UHFFFAOYSA-N 0.000 description 4
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 4
- 238000002835 absorbance Methods 0.000 description 4
- 229910052801 chlorine Inorganic materials 0.000 description 4
- 125000005843 halogen group Chemical group 0.000 description 4
- 229920000728 polyester Polymers 0.000 description 4
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- 239000002987 primer (paints) Substances 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 229910000679 solder Inorganic materials 0.000 description 4
- 150000003918 triazines Chemical class 0.000 description 4
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 4
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 3
- 229920013683 Celanese Polymers 0.000 description 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- 229920006385 Geon Polymers 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- 229920001944 Plastisol Polymers 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 238000000862 absorption spectrum Methods 0.000 description 3
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 3
- 230000002411 adverse Effects 0.000 description 3
- 125000003342 alkenyl group Chemical group 0.000 description 3
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 3
- 239000004327 boric acid Substances 0.000 description 3
- 239000000460 chlorine Substances 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
- 239000003112 inhibitor Substances 0.000 description 3
- 239000003999 initiator Substances 0.000 description 3
- 239000004973 liquid crystal related substance Substances 0.000 description 3
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- 229920000058 polyacrylate Polymers 0.000 description 3
- 229920013639 polyalphaolefin Polymers 0.000 description 3
- 229920001223 polyethylene glycol Polymers 0.000 description 3
- 230000006641 stabilisation Effects 0.000 description 3
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- 239000000126 substance Substances 0.000 description 3
- 125000005017 substituted alkenyl group Chemical group 0.000 description 3
- 125000004426 substituted alkynyl group Chemical group 0.000 description 3
- FCEHBMOGCRZNNI-UHFFFAOYSA-N 1-benzothiophene Chemical compound C1=CC=C2SC=CC2=C1 FCEHBMOGCRZNNI-UHFFFAOYSA-N 0.000 description 2
- UZKWTJUDCOPSNM-UHFFFAOYSA-N 1-ethenoxybutane Chemical compound CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- 244000043261 Hevea brasiliensis Species 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 2
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Images
Classifications
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B5/00—Optical elements other than lenses
- G02B5/30—Polarising elements
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B5/00—Optical elements other than lenses
- G02B5/30—Polarising elements
- G02B5/3025—Polarisers, i.e. arrangements capable of producing a definite output polarisation state from an unpolarised input state
- G02B5/3033—Polarisers, i.e. arrangements capable of producing a definite output polarisation state from an unpolarised input state in the form of a thin sheet or foil, e.g. Polaroid
-
- 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
- C08F8/00—Chemical modification by after-treatment
-
- 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
- C08F8/00—Chemical modification by after-treatment
- C08F8/30—Introducing nitrogen atoms or nitrogen-containing groups
-
- 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
-
- 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
- C08F2800/00—Copolymer characterised by the proportions of the comonomers expressed
- C08F2800/20—Copolymer characterised by the proportions of the comonomers expressed as weight or mass percentages
Landscapes
- Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Laminated Bodies (AREA)
- Polarising Elements (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Treatments Of Macromolecular Shaped Articles (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10/117,774 US6949207B2 (en) | 2002-04-04 | 2002-04-04 | K-type polarizer and preparation thereof |
| PCT/US2003/003258 WO2003085427A1 (en) | 2002-04-04 | 2003-02-04 | K-type polarizer and preparation thereof |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2005527847A true JP2005527847A (ja) | 2005-09-15 |
| JP2005527847A5 JP2005527847A5 (enExample) | 2006-03-23 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2003582560A Withdrawn JP2005527847A (ja) | 2002-04-04 | 2003-02-04 | K型偏光子およびその製造 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US6949207B2 (enExample) |
| EP (1) | EP1493048A1 (enExample) |
| JP (1) | JP2005527847A (enExample) |
| KR (1) | KR20040093493A (enExample) |
| CN (1) | CN1329753C (enExample) |
| AU (1) | AU2003207824A1 (enExample) |
| WO (1) | WO2003085427A1 (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2016533540A (ja) * | 2013-09-30 | 2016-10-27 | エルジー・ケム・リミテッド | 薄型偏光子の製造方法、これを用いて製造された薄型偏光子および偏光板 |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
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| US7110178B2 (en) * | 2001-07-02 | 2006-09-19 | 3M Innovative Properties Company | Polarizers coated with optically functional layers |
| US20050073065A1 (en) * | 2002-04-06 | 2005-04-07 | Mack Jon M. | Process for making an intrinsic polarizer |
| US20040062682A1 (en) * | 2002-09-30 | 2004-04-01 | Rakow Neal Anthony | Colorimetric sensor |
| US7573637B2 (en) * | 2004-08-03 | 2009-08-11 | Seiko Epson Corporation | Intrinsic polarizer and method of manufacturing an intrinsic polarizer |
| US7391569B2 (en) * | 2004-12-29 | 2008-06-24 | 3M Innovative Properties Company | Projection system including intrinsic polarizer |
| US7329716B2 (en) * | 2005-04-18 | 2008-02-12 | Yazaki Corporation | Siloxane oligomers by phase transfer catalysis |
| US7329715B2 (en) * | 2005-04-18 | 2008-02-12 | Yazaki Corporation | Abrasion resistant coatings by siloxane oligomers |
| US7767143B2 (en) * | 2006-06-27 | 2010-08-03 | 3M Innovative Properties Company | Colorimetric sensors |
| US7651830B2 (en) * | 2007-06-01 | 2010-01-26 | 3M Innovative Properties Company | Patterned photoacid etching and articles therefrom |
| KR102102351B1 (ko) | 2013-04-25 | 2020-04-21 | 삼성디스플레이 주식회사 | 기능성 편광 필름 및 이를 채용하는 유기발광표시장치. |
| KR101648243B1 (ko) * | 2013-06-27 | 2016-08-12 | 제일모직주식회사 | 폴리엔 편광자, 이의 제조방법, 이를 포함하는 편광판 및 광학표시장치 |
| TWI526505B (zh) | 2014-09-11 | 2016-03-21 | 財團法人工業技術研究院 | 硬塗層組成物及應用其之偏光膜和顯示器 |
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| US2445555A (en) | 1945-04-16 | 1948-07-20 | Polaroid Corp | Light-polarizing polyvinyl sheet containing polyvinyl compoundboric acid complex |
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| US3914017A (en) | 1973-11-05 | 1975-10-21 | Polaroid Corp | K-sheet type polarizers prepared from polyvinyl alcohol graft copolymers |
| US3936538A (en) * | 1974-03-18 | 1976-02-03 | Calgon Consumer Products Company Inc. | Polymeric film dryer-added fabric softening compositions |
| US6630970B2 (en) * | 2001-07-02 | 2003-10-07 | 3M Innovative Properties Company | Polarizers for use with liquid crystal displays |
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| US4229498A (en) * | 1979-03-29 | 1980-10-21 | Toyo Boseki Kabushiki Kaisha | Light-polarizing film |
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| JPS5666307A (en) * | 1979-10-04 | 1981-06-04 | Hitachi Ltd | Rolling mill |
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| DE19502806A1 (de) | 1995-01-30 | 1996-08-01 | Bayer Ag | Thermostabile Polarisatoren |
| US5554664A (en) | 1995-03-06 | 1996-09-10 | Minnesota Mining And Manufacturing Company | Energy-activatable salts with fluorocarbon anions |
| US5578404A (en) * | 1995-03-27 | 1996-11-26 | Polaroid Corporation | Process for the production of liquid crystal display |
| US5666223A (en) | 1995-12-01 | 1997-09-09 | Polaroid Corporation | High-efficiency K-sheet polarizer |
| JP2873930B2 (ja) | 1996-02-13 | 1999-03-24 | 工業技術院長 | カーボンナノチューブを有する炭素質固体構造体、炭素質固体構造体からなる電子線源素子用電子放出体、及び炭素質固体構造体の製造方法 |
| DE69835729T2 (de) * | 1997-03-19 | 2007-09-20 | KURARAY CO., LTD, Kurashiki | Polarisationsfilm |
| US5847133A (en) | 1997-05-23 | 1998-12-08 | Minnesota Mining And Manufacturing Company | Ionic halomethyl-1,3,5-triazine photoinitiators |
| US5925289A (en) | 1997-06-20 | 1999-07-20 | Polaroid Corporation | Synthetic UV-bleached polarizer and method for the manufacture thereof |
| US5973834A (en) * | 1997-12-19 | 1999-10-26 | Polaroid Corporation | Method for the manufacture of a light-polarizing polyvinylene sheet |
| US6409328B1 (en) * | 1999-03-31 | 2002-06-25 | Fuji Photo Film Co., Ltd. | Method of forming images and material for image formation |
| EP1057623B1 (en) | 1999-06-04 | 2004-05-06 | Agfa-Gevaert | A method for preparing a lithographic printing plate by laser ablation of a heat-sensitive imaging element |
| CN1112597C (zh) * | 2000-04-17 | 2003-06-25 | 黄精忠 | K型偏振膜的制造方法 |
| US20030017856A1 (en) * | 2001-06-20 | 2003-01-23 | 3M Innovative Properties Company | Method for altering the appearance of liquid crystal displays using exchangable front polarizers |
| US7110178B2 (en) * | 2001-07-02 | 2006-09-19 | 3M Innovative Properties Company | Polarizers coated with optically functional layers |
-
2002
- 2002-04-04 US US10/117,774 patent/US6949207B2/en not_active Expired - Fee Related
-
2003
- 2003-02-04 KR KR10-2004-7015623A patent/KR20040093493A/ko not_active Ceased
- 2003-02-04 CN CNB038078090A patent/CN1329753C/zh not_active Expired - Fee Related
- 2003-02-04 AU AU2003207824A patent/AU2003207824A1/en not_active Abandoned
- 2003-02-04 JP JP2003582560A patent/JP2005527847A/ja not_active Withdrawn
- 2003-02-04 EP EP03706062A patent/EP1493048A1/en not_active Withdrawn
- 2003-02-04 WO PCT/US2003/003258 patent/WO2003085427A1/en not_active Ceased
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2016533540A (ja) * | 2013-09-30 | 2016-10-27 | エルジー・ケム・リミテッド | 薄型偏光子の製造方法、これを用いて製造された薄型偏光子および偏光板 |
Also Published As
| Publication number | Publication date |
|---|---|
| KR20040093493A (ko) | 2004-11-05 |
| EP1493048A1 (en) | 2005-01-05 |
| WO2003085427A8 (en) | 2003-12-18 |
| WO2003085427A1 (en) | 2003-10-16 |
| CN1329753C (zh) | 2007-08-01 |
| AU2003207824A1 (en) | 2003-10-20 |
| US20030189264A1 (en) | 2003-10-09 |
| US6949207B2 (en) | 2005-09-27 |
| CN1646953A (zh) | 2005-07-27 |
| AU2003207824A8 (en) | 2003-10-20 |
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