KR20060014372A - 고유 편광체의 제조 방법 - Google Patents
고유 편광체의 제조 방법 Download PDFInfo
- Publication number
- KR20060014372A KR20060014372A KR1020057018492A KR20057018492A KR20060014372A KR 20060014372 A KR20060014372 A KR 20060014372A KR 1020057018492 A KR1020057018492 A KR 1020057018492A KR 20057018492 A KR20057018492 A KR 20057018492A KR 20060014372 A KR20060014372 A KR 20060014372A
- Authority
- KR
- South Korea
- Prior art keywords
- polymer film
- film
- stretching
- polymer
- aqueous
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 13
- 229920006254 polymer film Polymers 0.000 claims abstract description 74
- 230000018044 dehydration Effects 0.000 claims abstract description 49
- 238000006297 dehydration reaction Methods 0.000 claims abstract description 49
- 239000003054 catalyst Substances 0.000 claims abstract description 46
- 238000010438 heat treatment Methods 0.000 claims abstract description 16
- 229920000642 polymer Polymers 0.000 claims abstract description 15
- 125000005678 ethenylene group Chemical group [H]C([*:1])=C([H])[*:2] 0.000 claims abstract description 8
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 84
- 238000000034 method Methods 0.000 claims description 51
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 42
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 37
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 claims description 19
- 239000004327 boric acid Substances 0.000 claims description 19
- 238000005885 boration reaction Methods 0.000 claims description 17
- 229910021538 borax Inorganic materials 0.000 claims description 16
- 239000004328 sodium tetraborate Substances 0.000 claims description 16
- 235000010339 sodium tetraborate Nutrition 0.000 claims description 16
- 239000001043 yellow dye Substances 0.000 claims description 16
- 239000000975 dye Substances 0.000 claims description 15
- 239000007864 aqueous solution Substances 0.000 claims description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical group O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 14
- AJDUTMFFZHIJEM-UHFFFAOYSA-N n-(9,10-dioxoanthracen-1-yl)-4-[4-[[4-[4-[(9,10-dioxoanthracen-1-yl)carbamoyl]phenyl]phenyl]diazenyl]phenyl]benzamide Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2NC(=O)C(C=C1)=CC=C1C(C=C1)=CC=C1N=NC(C=C1)=CC=C1C(C=C1)=CC=C1C(=O)NC1=CC=CC2=C1C(=O)C1=CC=CC=C1C2=O AJDUTMFFZHIJEM-UHFFFAOYSA-N 0.000 claims description 11
- 230000008569 process Effects 0.000 claims description 10
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 9
- 239000012736 aqueous medium Substances 0.000 claims description 7
- 229920002554 vinyl polymer Polymers 0.000 claims description 7
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 6
- 239000008367 deionised water Substances 0.000 claims description 6
- 229910021641 deionized water Inorganic materials 0.000 claims description 6
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid group Chemical group S(O)(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 6
- 239000001045 blue dye Substances 0.000 claims description 5
- 230000002457 bidirectional effect Effects 0.000 claims description 4
- BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 claims description 3
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 3
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 claims description 3
- 229940071870 hydroiodic acid Drugs 0.000 claims description 3
- 238000007598 dipping method Methods 0.000 claims 4
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 claims 2
- 125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 claims 2
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- 235000019422 polyvinyl alcohol Nutrition 0.000 description 39
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- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 10
- 238000000576 coating method Methods 0.000 description 10
- 238000006116 polymerization reaction Methods 0.000 description 10
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 9
- 239000011248 coating agent Substances 0.000 description 9
- 239000004014 plasticizer Substances 0.000 description 9
- 238000005259 measurement Methods 0.000 description 8
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- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 239000013068 control sample Substances 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
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- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
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- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
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- 238000002360 preparation method Methods 0.000 description 2
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- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Inorganic materials [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 2
- 238000001228 spectrum Methods 0.000 description 2
- PQVHMOLNSYFXIJ-UHFFFAOYSA-N 4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]-1-[2-oxo-2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethyl]pyrazole-3-carboxylic acid Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C=1C(=NN(C=1)CC(N1CC2=C(CC1)NN=N2)=O)C(=O)O PQVHMOLNSYFXIJ-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- 229920002799 BoPET Polymers 0.000 description 1
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 1
- 229920001634 Copolyester Polymers 0.000 description 1
- 101100338765 Danio rerio hamp2 gene Proteins 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 101150043052 Hamp gene Proteins 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 239000005041 Mylar™ Substances 0.000 description 1
- 239000000020 Nitrocellulose Substances 0.000 description 1
- 239000006057 Non-nutritive feed additive Substances 0.000 description 1
- SJEYSFABYSGQBG-UHFFFAOYSA-M Patent blue Chemical compound [Na+].C1=CC(N(CC)CC)=CC=C1C(C=1C(=CC(=CC=1)S([O-])(=O)=O)S([O-])(=O)=O)=C1C=CC(=[N+](CC)CC)C=C1 SJEYSFABYSGQBG-UHFFFAOYSA-M 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- 229920004890 Triton X-100 Polymers 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
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- 150000007513 acids Chemical class 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 239000008186 active pharmaceutical agent Substances 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 1
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- MFZGSFUTGDGCSC-UHFFFAOYSA-L disodium;3-[[3-methoxy-4-[[2-methoxy-4-[(3-sulfonatophenyl)diazenyl]phenyl]carbamoylamino]phenyl]diazenyl]benzenesulfonate Chemical compound [Na+].[Na+].COC1=CC(N=NC=2C=C(C=CC=2)S([O-])(=O)=O)=CC=C1NC(=O)NC(C(=C1)OC)=CC=C1N=NC1=CC=CC(S([O-])(=O)=O)=C1 MFZGSFUTGDGCSC-UHFFFAOYSA-L 0.000 description 1
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- 230000007935 neutral effect Effects 0.000 description 1
- 229920001220 nitrocellulos Polymers 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 238000005192 partition Methods 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
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- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
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- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
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- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- WUUHFRRPHJEEKV-UHFFFAOYSA-N tripotassium borate Chemical compound [K+].[K+].[K+].[O-]B([O-])[O-] WUUHFRRPHJEEKV-UHFFFAOYSA-N 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
Images
Classifications
-
- 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
-
- 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
- C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
- C08J7/12—Chemical modification
-
- 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
- C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
- C08J7/12—Chemical modification
- C08J7/14—Chemical modification with acids, their salts or anhydrides
-
- 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
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2329/00—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal, or ketal radical; Hydrolysed polymers of esters of unsaturated alcohols with saturated carboxylic acids; Derivatives of such polymer
-
- 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
- C08J2329/00—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal, or ketal radical; Hydrolysed polymers of esters of unsaturated alcohols with saturated carboxylic acids; Derivatives of such polymer
- C08J2329/02—Homopolymers or copolymers of unsaturated alcohols
- C08J2329/04—Polyvinyl alcohol; Partially hydrolysed homopolymers or copolymers of esters of unsaturated alcohols with saturated carboxylic acids
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Manufacturing & Machinery (AREA)
- Engineering & Computer Science (AREA)
- Physics & Mathematics (AREA)
- General Chemical & Material Sciences (AREA)
- Materials Engineering (AREA)
- General Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
- Polarising Elements (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Shaping By String And By Release Of Stress In Plastics And The Like (AREA)
- Treatments Of Macromolecular Shaped Articles (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10/403,885 US20050073065A1 (en) | 2002-04-06 | 2003-03-31 | Process for making an intrinsic polarizer |
| US10/403,885 | 2003-03-31 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR20060014372A true KR20060014372A (ko) | 2006-02-15 |
Family
ID=33309457
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020057018492A Withdrawn KR20060014372A (ko) | 2003-03-31 | 2004-03-15 | 고유 편광체의 제조 방법 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US20050073065A1 (enExample) |
| EP (1) | EP1611191A1 (enExample) |
| JP (1) | JP2006522365A (enExample) |
| KR (1) | KR20060014372A (enExample) |
| CN (1) | CN1768095B (enExample) |
| TW (1) | TW200508291A (enExample) |
| WO (1) | WO2004094510A1 (enExample) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2008097007A1 (en) * | 2007-02-09 | 2008-08-14 | Lg Chem, Ltd. | Polarizer having excellent durability, polarizing plate and methods of producing the polarizer and the polarizing plate |
| KR100958288B1 (ko) * | 2007-02-09 | 2010-05-19 | 주식회사 엘지화학 | 직교투과도가 개선된 요오드계 편광 소자, 편광판 및 그제조 방법 |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| 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 |
| US7846541B2 (en) * | 2007-11-02 | 2010-12-07 | Seiko Epson Corporation | Optical element having optical adhesive layer and polarizer |
| US20090163686A1 (en) * | 2007-12-20 | 2009-06-25 | 3M Innovative Properties Company | Method of making an intrinsic polarizer |
| JP5525213B2 (ja) | 2009-08-28 | 2014-06-18 | 富士フイルム株式会社 | 偏光膜、積層体、及び液晶表示装置 |
| JP5657243B2 (ja) | 2009-09-14 | 2015-01-21 | ユー・ディー・シー アイルランド リミテッド | カラーフィルタ及び発光表示素子 |
| JP2015001584A (ja) * | 2013-06-14 | 2015-01-05 | 株式会社ポラテクノ | 固有偏光子 |
| JP6245879B2 (ja) * | 2013-07-30 | 2017-12-13 | サムスン エスディアイ カンパニー, リミテッドSamsung Sdi Co., Ltd. | ポリエン（ｐｏｌｙｅｎｅ）系偏光フィルム（ｆｉｌｍ）の製造方法、ポリエン系偏光フィルム、積層偏光フィルム、及び表示装置 |
| JP7382974B2 (ja) * | 2019-02-08 | 2023-11-17 | 日東電工株式会社 | 偏光膜、偏光板、および該偏光膜の製造方法 |
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| US2445555A (en) * | 1945-04-16 | 1948-07-20 | Polaroid Corp | Light-polarizing polyvinyl sheet containing polyvinyl compoundboric acid complex |
| GB884469A (en) * | 1958-12-18 | 1961-12-13 | American Optical Corp | Improvements in light polarisers and methods of making them |
| US3914017A (en) * | 1973-11-05 | 1975-10-21 | Polaroid Corp | K-sheet type polarizers prepared from polyvinyl alcohol graft copolymers |
| JPS5648601A (en) * | 1979-09-27 | 1981-05-01 | Nitto Electric Ind Co Ltd | Polarizing film |
| US4396642A (en) * | 1981-11-24 | 1983-08-02 | American Hoechst Corporation | Hydrolytically stabilized polarizer |
| US4842781A (en) * | 1984-02-29 | 1989-06-27 | Mitsui Toatsu Chemicals, Inc. | Colored polarizing film and method of making same |
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| US6808657B2 (en) * | 2002-02-12 | 2004-10-26 | 3M Innovative Properties Company | Process for preparing a K-type polarizer |
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| US20030189275A1 (en) * | 2002-04-06 | 2003-10-09 | Cael John J. | Enhanced intrinsic polarizer |
| WO2004059370A2 (en) * | 2002-12-20 | 2004-07-15 | Vision-Ease Lens, Inc. | Polarizing plate and eyewear plastic article containing the same |
-
2003
- 2003-03-31 US US10/403,885 patent/US20050073065A1/en not_active Abandoned
-
2004
- 2004-03-15 WO PCT/US2004/007907 patent/WO2004094510A1/en not_active Ceased
- 2004-03-15 EP EP04759605A patent/EP1611191A1/en not_active Withdrawn
- 2004-03-15 JP JP2006507214A patent/JP2006522365A/ja not_active Withdrawn
- 2004-03-15 KR KR1020057018492A patent/KR20060014372A/ko not_active Withdrawn
- 2004-03-15 CN CN2004800087546A patent/CN1768095B/zh not_active Expired - Fee Related
- 2004-03-30 TW TW093108698A patent/TW200508291A/zh unknown
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2008097007A1 (en) * | 2007-02-09 | 2008-08-14 | Lg Chem, Ltd. | Polarizer having excellent durability, polarizing plate and methods of producing the polarizer and the polarizing plate |
| KR100958287B1 (ko) * | 2007-02-09 | 2010-05-19 | 주식회사 엘지화학 | 내구성이 우수한 편광 소자, 편광판 및 그 제조 방법 |
| KR100958288B1 (ko) * | 2007-02-09 | 2010-05-19 | 주식회사 엘지화학 | 직교투과도가 개선된 요오드계 편광 소자, 편광판 및 그제조 방법 |
| US8094375B2 (en) | 2007-02-09 | 2012-01-10 | Lg Chem, Ltd. | Iodine-type polarizer, polarizing plate and method for producing thereof |
| US8609764B2 (en) | 2007-02-09 | 2013-12-17 | Lg Chem, Ltd. | Polarizer having excellent durability, polarizing plate and methods of producing the polarizer and the polarizing plate |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2004094510A1 (en) | 2004-11-04 |
| US20050073065A1 (en) | 2005-04-07 |
| CN1768095B (zh) | 2010-05-26 |
| EP1611191A1 (en) | 2006-01-04 |
| CN1768095A (zh) | 2006-05-03 |
| JP2006522365A (ja) | 2006-09-28 |
| TW200508291A (en) | 2005-03-01 |
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