WO2004019086A1 - 偏光子、それを用いた光学フィルム、それらを用いた画像表示装置 - Google Patents
偏光子、それを用いた光学フィルム、それらを用いた画像表示装置 Download PDFInfo
- Publication number
- WO2004019086A1 WO2004019086A1 PCT/JP2003/009367 JP0309367W WO2004019086A1 WO 2004019086 A1 WO2004019086 A1 WO 2004019086A1 JP 0309367 W JP0309367 W JP 0309367W WO 2004019086 A1 WO2004019086 A1 WO 2004019086A1
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- WO
- WIPO (PCT)
- Prior art keywords
- polarizer
- film
- liquid crystal
- polarizing plate
- light
- Prior art date
Links
- 239000012788 optical film Substances 0.000 title claims description 42
- 239000004973 liquid crystal related substance Substances 0.000 claims abstract description 103
- 239000000126 substance Substances 0.000 claims abstract description 19
- 238000010521 absorption reaction Methods 0.000 claims abstract description 17
- 239000011159 matrix material Substances 0.000 claims abstract description 6
- 238000005401 electroluminescence Methods 0.000 claims abstract 2
- 239000010408 film Substances 0.000 claims description 124
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- 229920006254 polymer film Polymers 0.000 claims description 49
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- 230000010287 polarization Effects 0.000 claims description 39
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- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 69
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- 239000004327 boric acid Substances 0.000 description 28
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 26
- 238000004132 cross linking Methods 0.000 description 23
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- 229910052751 metal Inorganic materials 0.000 description 14
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- -1 polyethylene terephthalate Polymers 0.000 description 10
- 230000008569 process Effects 0.000 description 10
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- 239000004986 Cholesteric liquid crystals (ChLC) Substances 0.000 description 9
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- 238000002834 transmittance Methods 0.000 description 8
- 238000004040 coloring Methods 0.000 description 7
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 7
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 6
- 239000003431 cross linking reagent Substances 0.000 description 6
- 239000000975 dye Substances 0.000 description 6
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- 229920000642 polymer Polymers 0.000 description 6
- 229920001296 polysiloxane Polymers 0.000 description 6
- FVAUCKIRQBBSSJ-UHFFFAOYSA-M sodium iodide Chemical compound [Na+].[I-] FVAUCKIRQBBSSJ-UHFFFAOYSA-M 0.000 description 6
- 238000005406 washing Methods 0.000 description 6
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 5
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- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 3
- 239000004793 Polystyrene Substances 0.000 description 3
- NNLVGZFZQQXQNW-ADJNRHBOSA-N [(2r,3r,4s,5r,6s)-4,5-diacetyloxy-3-[(2s,3r,4s,5r,6r)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6s)-4,5,6-triacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxyoxan-2-yl]methyl acetate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](OC(C)=O)[C@H]1OC(C)=O)O[C@H]1[C@@H]([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1)OC(C)=O)COC(=O)C)[C@@H]1[C@@H](COC(C)=O)O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O NNLVGZFZQQXQNW-ADJNRHBOSA-N 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
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- 230000000052 comparative effect Effects 0.000 description 3
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- 235000011187 glycerol Nutrition 0.000 description 3
- 229910052740 iodine Inorganic materials 0.000 description 3
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- 239000005020 polyethylene terephthalate Substances 0.000 description 3
- 229920000139 polyethylene terephthalate Polymers 0.000 description 3
- 238000004080 punching Methods 0.000 description 3
- 238000011160 research Methods 0.000 description 3
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 2
- 239000004593 Epoxy Substances 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 229920006257 Heat-shrinkable film Polymers 0.000 description 2
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical compound CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 2
- 239000004977 Liquid-crystal polymers (LCPs) Substances 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 239000004952 Polyamide Substances 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
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 2
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- 239000011888 foil Substances 0.000 description 2
- 239000011630 iodine Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- HSZCZNFXUDYRKD-UHFFFAOYSA-M lithium iodide Chemical compound [Li+].[I-] HSZCZNFXUDYRKD-UHFFFAOYSA-M 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- SEEYREPSKCQBBF-UHFFFAOYSA-N n-methylmaleimide Chemical compound CN1C(=O)C=CC1=O SEEYREPSKCQBBF-UHFFFAOYSA-N 0.000 description 2
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- 235000009518 sodium iodide Nutrition 0.000 description 2
- 239000004328 sodium tetraborate Substances 0.000 description 2
- 235000010339 sodium tetraborate Nutrition 0.000 description 2
- UAYWVJHJZHQCIE-UHFFFAOYSA-L zinc iodide Chemical compound I[Zn]I UAYWVJHJZHQCIE-UHFFFAOYSA-L 0.000 description 2
- 229910001148 Al-Li alloy Inorganic materials 0.000 description 1
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 1
- UNMYWSMUMWPJLR-UHFFFAOYSA-L Calcium iodide Chemical compound [Ca+2].[I-].[I-] UNMYWSMUMWPJLR-UHFFFAOYSA-L 0.000 description 1
- 229920002101 Chitin Polymers 0.000 description 1
- 229920001661 Chitosan Polymers 0.000 description 1
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- 239000004985 Discotic Liquid Crystal Substance Substances 0.000 description 1
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- SXRSQZLOMIGNAQ-UHFFFAOYSA-N Glutaraldehyde Chemical compound O=CCCCC=O SXRSQZLOMIGNAQ-UHFFFAOYSA-N 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 229910019015 Mg-Ag Inorganic materials 0.000 description 1
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- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 1
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- 238000012648 alternating copolymerization Methods 0.000 description 1
- CECABOMBVQNBEC-UHFFFAOYSA-K aluminium iodide Chemical compound I[Al](I)I CECABOMBVQNBEC-UHFFFAOYSA-K 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 229910000410 antimony oxide Inorganic materials 0.000 description 1
- SGUXGJPBTNFBAD-UHFFFAOYSA-L barium iodide Chemical compound [I-].[I-].[Ba+2] SGUXGJPBTNFBAD-UHFFFAOYSA-L 0.000 description 1
- 229910001638 barium iodide Inorganic materials 0.000 description 1
- 229940075444 barium iodide Drugs 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 150000008366 benzophenones Chemical class 0.000 description 1
- 125000003354 benzotriazolyl group Chemical class N1N=NC2=C1C=CC=C2* 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 125000005619 boric acid group Chemical group 0.000 description 1
- 150000001639 boron compounds Chemical class 0.000 description 1
- CXKCTMHTOKXKQT-UHFFFAOYSA-N cadmium oxide Inorganic materials [Cd]=O CXKCTMHTOKXKQT-UHFFFAOYSA-N 0.000 description 1
- CFEAAQFZALKQPA-UHFFFAOYSA-N cadmium(2+);oxygen(2-) Chemical compound [O-2].[Cd+2] CFEAAQFZALKQPA-UHFFFAOYSA-N 0.000 description 1
- 229910001640 calcium iodide Inorganic materials 0.000 description 1
- 229940046413 calcium iodide Drugs 0.000 description 1
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- GBRBMTNGQBKBQE-UHFFFAOYSA-L copper;diiodide Chemical compound I[Cu]I GBRBMTNGQBKBQE-UHFFFAOYSA-L 0.000 description 1
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- 229920001477 hydrophilic polymer Polymers 0.000 description 1
- 229910003437 indium oxide Inorganic materials 0.000 description 1
- PJXISJQVUVHSOJ-UHFFFAOYSA-N indium(iii) oxide Chemical compound [O-2].[O-2].[O-2].[In+3].[In+3] PJXISJQVUVHSOJ-UHFFFAOYSA-N 0.000 description 1
- AMGQUBHHOARCQH-UHFFFAOYSA-N indium;oxotin Chemical compound [In].[Sn]=O AMGQUBHHOARCQH-UHFFFAOYSA-N 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 150000004694 iodide salts Chemical class 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
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- 230000007246 mechanism Effects 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 238000001465 metallisation Methods 0.000 description 1
- CWQXQMHSOZUFJS-UHFFFAOYSA-N molybdenum disulfide Chemical compound S=[Mo]=S CWQXQMHSOZUFJS-UHFFFAOYSA-N 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 125000002080 perylenyl group Chemical group C1(=CC=C2C=CC=C3C4=CC=CC5=CC=CC(C1=C23)=C45)* 0.000 description 1
- 238000007747 plating Methods 0.000 description 1
- 229920000636 poly(norbornene) polymer Polymers 0.000 description 1
- 229920002492 poly(sulfone) Polymers 0.000 description 1
- 229920001197 polyacetylene Polymers 0.000 description 1
- 229920001230 polyarylate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
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- 150000004291 polyenes Chemical class 0.000 description 1
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- 150000008442 polyphenolic compounds Chemical class 0.000 description 1
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- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- SCUZVMOVTVSBLE-UHFFFAOYSA-N prop-2-enenitrile;styrene Chemical compound C=CC#N.C=CC1=CC=CC=C1 SCUZVMOVTVSBLE-UHFFFAOYSA-N 0.000 description 1
- 230000006798 recombination Effects 0.000 description 1
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- 239000002356 single layer Substances 0.000 description 1
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- 239000006104 solid solution Substances 0.000 description 1
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- 238000010186 staining Methods 0.000 description 1
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 1
- 229910001887 tin oxide Inorganic materials 0.000 description 1
- QPBYLOWPSRZOFX-UHFFFAOYSA-J tin(iv) iodide Chemical compound I[Sn](I)(I)I QPBYLOWPSRZOFX-UHFFFAOYSA-J 0.000 description 1
- NLLZTRMHNHVXJJ-UHFFFAOYSA-J titanium tetraiodide Chemical compound I[Ti](I)(I)I NLLZTRMHNHVXJJ-UHFFFAOYSA-J 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 125000006617 triphenylamine group Chemical group 0.000 description 1
- 238000001771 vacuum deposition Methods 0.000 description 1
- 150000003752 zinc compounds Chemical class 0.000 description 1
Classifications
-
- 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
-
- 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
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B5/00—Optical elements other than lenses
- G02B5/30—Polarising elements
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K59/00—Integrated devices, or assemblies of multiple devices, comprising at least one organic light-emitting element covered by group H10K50/00
- H10K59/80—Constructional details
- H10K59/8791—Arrangements for improving contrast, e.g. preventing reflection of ambient light
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K50/00—Organic light-emitting devices
- H10K50/80—Constructional details
- H10K50/86—Arrangements for improving contrast, e.g. preventing reflection of ambient light
Definitions
- the present invention relates to a polarizer, an optical film such as a polarizing plate using the polarizer, and an image display device.
- Liquid crystal display devices are widely used in desktop electronic calculators, electronic clocks, personal computers, word processors, and instruments for automobiles and machines.
- Such a liquid crystal display device usually includes a polarizing plate for visualizing a change in the orientation of liquid crystal, and this polarizing plate has a very large effect on the display characteristics of the liquid crystal display device.
- a protective film such as triacetyl cellulose is laminated on both surfaces of a polarizer (polarizing film) such as a polyvinyl alcohol-based film in which a dichroic substance such as iodine or an organic dye is adsorbed and oriented.
- a polarizer such as a polyvinyl alcohol-based film in which a dichroic substance such as iodine or an organic dye is adsorbed and oriented.
- a polarizer that can provide a liquid crystal display device that is bright, has good color reproducibility, and has excellent display characteristics is desired.
- Japanese Patent Application Laid-Open No. 14-08939 discloses a polarizing plate using a polyvinyl alcohol-based polymer film which can be easily stretched uniformly. . Disclosure of the invention
- the polarizer of the present invention is a polarizer containing a dichroic substance in a matrix, and has an in-plane retardation in a range of 950 to 135 nm at a measurement wavelength that does not show absorption. It is characterized by.
- the present inventors have found that the phase difference of the polarizer itself is involved in the above-mentioned display unevenness, and have conducted intensive research.
- the in-plane retardation at the measurement wavelength that does not show the absorption is in the range of 950 to 135 nm, for example, even if the polarizer has a variation in the phase difference, the variation does not occur. It has been found that it has the effect of being difficult to see.
- the polarizer shows blue shading due to uneven dyeing or the like, if the polarizer exhibiting in-plane retardation as in the present invention is arranged in crossed nicols, the polarizer exhibits blue, so that the blue shading is obtained.
- FIG. 1 is a sectional view showing an example of the optical film of the present invention.
- FIG. 2 is a cross-sectional view showing another example of the optical film of the present invention.
- FIG. 3 is a sectional view showing an example of the liquid crystal panel of the present invention.
- FIG. 4 is a sectional view showing another example of the liquid crystal panel of the present invention.
- FIG. 5A is a cross-sectional view showing still another example of the liquid crystal panel of the present invention
- FIGS. 5B and 5C are partial cross-sectional views of the above-mentioned (A).
- FIG. 6 is a cross-sectional view of an example of the pack light according to the embodiment of the present invention.
- FIG. 7 is a cross-sectional view of another example of the packlight in the embodiment.
- FIG. 8 is a cross-sectional view of another example of the backlight in the embodiment.
- FIG. 9A is a cross-sectional view of still another example of the knock light in the embodiment
- FIG. 9B is a partial schematic view of the above-described (A).
- the polarizer of the present invention is a polarizer containing a dichroic substance in a matrix as described above, and has an in-plane retardation of 950 to 135 nm at a measurement wavelength that does not show absorption. It is characterized by being a range.
- the in-plane retardation is preferably set in the range of 150 to 125 nm, more preferably in the range of 110 to 1200 nm.
- the in-plane retardation ( ⁇ nd) is represented by the following equation, where n X and ny indicate the refractive indexes of the polarizer in the X-axis and Y-axis directions, respectively, Is the axial direction showing the maximum refractive index in the plane of the polarizer, Y axis The direction is an axial direction perpendicular to the X axis in the plane, and d indicates the thickness of the polarizer.
- the in-plane retardation is, for example, the size of the polarizer is set to 8 to 800 cm ⁇ 15 to 1500 cm, and a total of 28 to 1,200,000 measurement points are set every l to 20 mm in length and width.
- the phase difference is measured in, it is preferable that all the measured values fall within the above range.
- the measurement wavelength is not particularly limited as long as the wavelength at which the polarizer of the present invention does not show absorption, that is, the wavelength at which the dichroic substance does not show absorption, for example, 800 to 1500 nm, preferably It is 840 to 1200 nm, particularly preferably 1000 nm.
- the measurement wavelength for example, when the measurement wavelength is X (nm), it is necessary to consider the chromatic dispersion ARx expressed by the following formula. In the case of the absorption edge and x a, it is necessary that x> x a.
- the differential phase difference change ( ⁇ ) of the in-plane retardation is in the range of 15 nmZmm to 5 nm / mm at the measurement wavelength not exhibiting the absorption.
- the differential phase difference change amount ( ⁇ ) is in such a range, for example, an effect of exhibiting high uniformity is exhibited particularly on a large-screen display such as an LCD television.
- Differential phase difference change ( ⁇ ) Is more preferably in the range of 4 nmZmm to 4 nmmm, particularly preferably in the range of 1.5 nmZmm to 2.5 nm / mm.
- the distance between the measurement points is preferably from 1 to 100 mm, and more preferably from 3 to 70 mm, from the viewpoint of accurately determining a locally occurring phase difference change.
- the distance between the measurement part showing the maximum value and the measurement part showing the minimum value is smaller.
- it is 10 mm or less (exceeds 0) or 100 mm or more, and the difference (in-plane retardation variation) between the maximum value and the minimum value is less than 60 nm.
- the distance is 7 mm or less or 120 mm or more, and the in-plane retardation difference is less than 45 nm, more preferably, the distance is 5 mm or less or 150 mm or more, and The in-plane retardation variation is less than 45 nm.
- the distance is as short as 10 mm or less, the maximum value and the minimum value are very close to each other, so that it is difficult to see the phase difference.
- the dispersion of the in-plane retardation becomes gentle, and the retardation dispersion of the polarizer becomes more difficult to see, so that it is more preferably 100 mm or more, and particularly preferably. 1 50 mm or more.
- the upper limit of the distance is not limited, and corresponds to the size of the film.
- Such a polarizer of the present invention is applied to, for example, a polarizing plate or an optical film, and is further used for various image display devices such as a liquid crystal display device. For this reason, for example, a polarizer that has been cut (so-called “chip cut”) in advance according to the size of the liquid crystal cell or the like may be used.
- a polarizer of the present invention can be produced, for example, by subjecting a polymer film to a swelling treatment, a dyeing treatment with a dichroic substance, a cross-linking treatment, a stretching treatment, and a water-washing treatment, as shown below. .
- the present invention is characterized in that, among polarizers, the in-plane retardation is selected within the above range, and the production itself of a polarizer satisfying the in-plane retardation is applied to by those skilled in the art. It can be done based on common technical knowledge at the time.
- the polymer film is not particularly limited, and a conventionally known film can be used. Examples thereof include polyvinyl alcohol (PVA) film, partially formalized PVA film, polyethylene terephthalate (PET), and the like. Examples thereof include hydrophilic polymer films such as an ethylene-biel acetate copolymer-based film and partially saponified films thereof. In addition to these, a polyene oriented film such as a dehydrated product of PVA or a dehydrochlorinated product of polyvinyl chloride, and a stretched oriented polypinylene film can also be used. Among these, a PVA-based polymer film is preferable because of its excellent dyeability with the dichroic substance iodine.
- the length in the stretching direction is hereinafter referred to as “length”
- the length in the stretching direction and the vertical direction is hereinafter referred to as “width”.
- the PVA film preferably has a degree of polymerization in the range of, for example, 170 to 4500, more preferably 2400 to 4000, and a crystallinity of 18 to 50%. And more preferably 23 to 47%.
- the glycerin content of the film is, for example, preferably in the range of 7 to 20% by weight, and more preferably in the range of 8 to 18% by weight.
- the thickness of the polymer film is not particularly limited. It is preferably in the range of 8080 zm, more preferably 70-85 m.
- the local thickness variation is preferably 0.7 m / cm or less, more preferably 0.5 m / cm or less, particularly preferably 0.2 m / cm or less with respect to the average thickness. m / cm or less. Further, even if the thickness of the polymer film exceeds 0.7 m / cm, for example, swelling treatment, cross-linking treatment, stretching treatment and the like described below are optimized, and liquid drainage is controlled. Thus, the influence of the thickness variation can be avoided.
- the local thickness variation is less than 0. 0 m / cm with respect to the average thickness
- the thickness variation between two points 1 to 100 mm apart that is, “ This means that the difference Z between the two points in the thickness Z is the distance between the two points is 0.7 / zm / cm or less.
- the average thickness is not particularly limited. For example, in the case of a PVA-based film (raw material) having a maximum width of 2600 mm, 2600 points may be measured. Note that the present invention is not limited to this.
- the polymer film for example, it is preferable to use a film having a small swelling variation in the swelling treatment in the next step, that is, a film having a small thickness variation due to swelling.
- a film having a small swelling variation in the swelling treatment in the next step that is, a film having a small thickness variation due to swelling.
- variations in retardation, dichroic substance content, transmittance, and the like can be further reduced.
- a polymer film having no variation in glycerin content is also preferable.
- the solution of the swelling bath for example, water, an aqueous glycerin solution, an aqueous potassium iodide solution, or the like can be used.
- the conditions for the swelling treatment are not particularly limited, and the swelling treatment can be carried out in the same manner as in the past.
- a swelling bath at 20 to 30 ° C. may be used for 60 to 300 seconds (preferably 90 to 200 seconds). (40 seconds, more preferably 120 to 180 seconds). If the swelling time is 60 seconds or longer, for example, contamination of the dyeing bath in the subsequent dyeing step can be sufficiently avoided, so that the problem of long run property can be reduced and dyeing unevenness can be sufficiently prevented. If the swelling time is 300 seconds or less, the occurrence of breakage during stretching in the subsequent stretching step can be sufficiently suppressed.
- the polymer film By immersing in the swelling bath, the polymer film swells usually 1.1 to 1.5 times the length of the film (raw material) before swelling. Further, it is preferable to apply a stretching treatment in the swelling bath to 1 to 1.3 times (preferably 1.05 to 1.25 times) the swelling amount.
- the stretching ratio when the stretching ratio is reduced and the immersion time is lengthened, in order to remove the shear generated on the film, for example, rolls such as an expansive roll, a spiral roll, and a crown roll are placed in the swelling bath. It is preferable to set up. In particular, when the width of the web is long (for example, when the width exceeds about 3 m), it is preferable to install a roll in order to remove a central portion of the web.
- the polymer film preferably has a small swelling variation, specifically, the thickness variation after swelling is preferably 8% or less, more preferably 5% or less, and particularly preferably. 2.5% or less.
- the thickness variation after swelling is preferably 8% or less, more preferably 5% or less, and particularly preferably. 2.5% or less.
- the difference between the maximum value and the minimum value of the thickness, and the distance between the portion having the maximum value and the portion having the minimum value have the following relationship. That is, “(difference between maximum value and minimum value) / distance” is, for example, 5 m / cin or less, preferably 1.0 ffl / cm or less, more preferably 0.5 ffl / cin or less. is there.
- the distance is preferably 5 mm or less or 250 mm or more, more preferably 10 mm or less or 150 mm or more, and particularly preferably 20 mm or less or 100 mm or less.
- the polymer film is pulled up from the swelling bath, immersed in, for example, a dyeing bath containing a dichroic material, and further stretched uniaxially in the dyeing bath. That is, the dichroic substance is adsorbed on the polymer film by the immersion, and the dichroic substance is oriented in one direction by stretching.
- the dichroic substance a conventionally known substance can be used.
- organic dyes When the organic dye is used, for example, it is preferable to combine two or more types from the viewpoint of neutralizing the visible light region.
- an aqueous solution in which the dichroic substance is dissolved in a solvent can be used.
- a solvent for example, water can be used, but an organic solvent compatible with water may be further added.
- concentration of the dichroic substance in the solution is not particularly limited, but is generally in the range of 0.05 to 0.10% by weight, preferably 0.01 to 0.08% by weight.
- the immersion time of the polymer film in the dyeing bath is not particularly limited, but is, for example, in the range of 30 to 120 seconds, preferably 40 to 110 seconds, more preferably 50 to 100 seconds. is there.
- the temperature of the dyeing bath is usually from 10 to 35 ° C.
- the stretching magnification in this dyeing treatment is, for example, preferably in the range of 2 to 3.2 times, more preferably 2.2 to 3.1 times, the length of the polymer film (raw material) before swelling. And particularly preferably 2.4 to 3.0 times. If the stretching ratio is 2 times or more, for example, the occurrence of ripples in the film stretching direction (MD direction) is sufficiently suppressed, and there is no problem of uneven coloring, and if it is 3.2 times or less, for example. However, a sufficient degree of polarization can be maintained.
- the polymer film may cause uneven dyeing.
- various rolls as described above are arranged in the dyeing bath, and the screens formed on the polymer film by the rolls. May be removed. Further, before or after immersing the polymer film in a dyeing bath, the roll may be used to remove the screen.
- cross-linking agent a conventionally known substance can be used, and examples thereof include boric acid, borax, boron compounds such as dalioxal and dartalaldehyde. These may be used alone or in combination of two or more.
- solution of the crosslinking bath an aqueous solution in which the crosslinking agent is dissolved in a solvent can be used.
- solvent for example, water can be used, and it may further contain an organic solvent compatible with water.
- the concentration of the crosslinking agent in the solution is not particularly limited, but is generally in the range of 1 to 10% by weight, preferably 1.5 to 8% by weight.
- the crosslinking agent is boric acid, for example, it is in the range of 1.5 to 7% by weight, preferably 2 to 6% by weight.
- the aqueous solution may further include, in addition to the boric acid compound, potassium iodide, lithium iodide, sodium iodide, zinc iodide, aluminum iodide, It may contain an auxiliary agent such as iodide such as lead iodide, copper iodide, barium iodide, calcium iodide, tin iodide, titanium iodide and the like.
- the content of the auxiliary in the solution is usually in the range of 1 to 18% by weight, preferably 2 to 18% by weight.
- the auxiliary agent is potassium iodide, it is in the range of 2 to 15% by weight, preferably 5 to 14% by weight.
- the ratio (weight ratio) of boric acid and potassium iodide in the solution is, for example, usually in the range of 7: 1 to 1: 9, preferably 5: 5.
- the temperature of the crosslinking bath, which is in the range of 1 to 1: 5, is not particularly limited.
- the relationship between the temperature and the temperature of the crosslinking treatment described later shows “dyeing temperature ⁇ crosslinking temperature ⁇ elongation temperature”.
- the range is preferably from 8 to 75 ° C, more preferably from 20 to 70 ° C.
- the immersion time of the polymer film is not particularly limited, but is usually 25 to: L for 50 seconds, and preferably 5 to 30 seconds.
- the stretching ratio in this crosslinking treatment is, for example, 3.5 times or less, and preferably 3.3 times or less, with respect to the length of the raw material.
- the polymer film is pulled out of the crosslinking bath, immersed in a final stretching bath, and further stretched in this stretching bath. Note that the cross-linking treatment and the stretching treatment may be further repeated.
- the solution for the stretching bath is not particularly limited, and for example, a solution containing 5 of boric acid, potassium iodide, various metal salts, other iodide compounds, zinc compounds and the like can be used.
- a solvent for this solution for example, water, ethanol, or the like can be used.
- boric acid when boric acid is used, its concentration is usually in the range of 2 to 10% by weight, preferably 3 to 6% by weight.
- the concentration of boric acid in the stretching bath is preferably higher than the concentration of boric acid in the crosslinking bath.
- potassium iodide in combination. In this case, for example, it is preferable to set the concentration to be higher than the concentration of potassium iodide in the crosslinking bath.
- the concentration of the potassium iodide is usually in the range of 4 to 10% by weight, preferably 6 to 8% by weight.
- the concentration of potassium iodide in the elongation bath is preferably set to be higher than, for example, the concentration of pentaiodide rim in the crosslinking bath.
- the temperature of the stretching bath is usually in the range of 40 to 75 ° C., preferably 50 to 70 ° C.
- the stretching magnification in this stretching treatment is, for example, in the range of 5.5 to 6.5 times, preferably in the range of 5.8 to 6.4 times, more preferably in the range of 5.8 to 6.4 times the length of the raw material.
- the range is from 0 to 6.2 times.
- the stretching time is, for example, preferably from 35 seconds to 60 seconds, and more preferably from 40 seconds to 50 seconds.
- the polymer film is pulled up from the stretching bath, immersed in an iodide-containing aqueous solution, washed with water, and dried.
- an iodide-containing aqueous solution those described above can be used, and among them, for example, potassium iodide, sodium iodide and the like are preferable.
- water can be used as this solvent.
- the remaining boric acid used in the stretching treatment can be washed out of the polymer film by the iodide-containing aqueous solution.
- the concentration is, for example, preferably in the range of 0.5 to 20% by weight, more preferably 1 to 15% by weight, and particularly preferably 1.0 to 15% by weight. 5-7% by weight.
- the temperature of the aqueous solution is usually in the range of 15 to 4 Ot, preferably 20 to 35 ° C.
- the immersion time in the aqueous solution is usually 2 to 15 seconds, preferably 3 to 12 seconds.
- the number of times of water washing after immersion in the iodide-containing aqueous solution is not particularly limited.
- the width and thickness of the stretched polymer film satisfy the following conditions.
- the manufactured polarizer of the present invention has further improved neutrality.
- the polarizer of the present invention and a polarizing plate using the same When they are arranged in parallel Nicols, it can be said that yellowness can be further suppressed, and when they are arranged perpendicularly, blueness and redness can be further suppressed. That is, when the total stretching ratio (magnification with respect to the raw material) of the stretching performed so far is a (hereinafter the same), the width of the stretched polymer film is the width of the polymer film (raw material) before swelling.
- the range is (l / ⁇ a X 100)% to (l / "a X 125)%, preferably (1 / a X 100)% to (1 / ⁇ & X 120)%, More preferably, it is preferably deformed to (1 / aX100)% to (1 / aX110)%.
- the stretching ratio a is 6, 41 to 51% is preferable.
- the width of the polymer film is, as described above, the length in the stretching direction (length direction) and the length in the vertical direction.
- the stretched polymer film when the stretched polymer film is not stretched uniformly, a gradient may occur in its thickness.
- the thinnest portion is (1 / ⁇ & X 80)% to (l / a X 100)%, preferably ( 1 / aX85)% to (: 1 / aX100)%, and more preferably (l / ⁇ TaX90)% to (1 / aX100)%.
- the thinnest part of the film tends to become thinner due to shrinkage of the periphery and other parts in the width direction, so that uniaxiality is reduced, optical characteristics are locally reduced, and unevenness is likely to be remarkable. Because there is.
- the width and the thickness preferably satisfy the following relationship. That is, the value represented by the following formula (I) is, for example, in the range of 0.9 to 1.1, and preferably in the range of 0.95 to 1.05. (T b XW b ) / (T a XW a )
- the polarizer of the present invention in which the matrix contains a dichroic substance can be produced. Drying is not particularly limited, for example, natural drying, air drying, heating drying, etc., but in the case of heating drying, the temperature is usually 20 to 40 ° C, preferably in the range of 22 to 35 ° C. is there.
- the processing time is generally in the range of 0.5 to 5 minutes, preferably 1 to 4 minutes, more preferably 1.5 to 3 minutes.
- the thickness of the finally obtained polarizer of the present invention is not particularly limited, for example, it is preferably in the range of 5 to 40, more preferably 15 to 35 m, and particularly preferably 17 to 32. is there. For example, when the thickness is 5 or more, more excellent mechanical strength is exhibited, and when the thickness is 40 m or less, more excellent optical characteristics are obtained. It is easy to reduce the thickness.
- the optical film of the present invention includes the polarizer of the present invention. Examples of such an optical film are shown below.
- a first example of the optical film of the present invention includes, for example, a polarizing plate including the polarizer of the present invention and a transparent protective layer, wherein the transparent protective layer is disposed on at least one surface of the polarizer.
- the transparent protective layer may be disposed on only one surface of the polarizer, or may be disposed on both surfaces. When laminating on both sides, for example, the same type of transparent protective layer may be used, or different types of transparent protective layers may be used.
- the measurement can be performed by removing the transparent protective layer from the polarizing plate of the present invention using, for example, a solvent.
- the measurement can be performed with the polarizing plate as is.
- the moisture content is preferably, for example, 2 to 5%, more preferably 2.5 to 4.5%, Particularly preferably, it is in the range of 3 to 4%.
- FIG. 1 shows a cross-sectional view of an example of the polarizing plate.
- the polarizing plate 10 includes a polarizer 1 and two transparent protective layers 2, and the transparent protective layers 2 are disposed on both surfaces of the polarizer 1.
- the transparent protective layer 2 is not particularly limited, and a conventionally known transparent protective film can be used.
- the transparent protective layer 2 include those having excellent transparency, mechanical strength, heat stability, moisture barrier properties, isotropy, and the like. preferable.
- the material include cellulosic resins such as triacetylcellulose, polyesters, polyphenols, polyamides, polyimides, polyethersulfones, polysulfones, polystyrenes, acrylics, and acetates. And polyolefin-based transparent resins.
- the acrylic, urethane, acrylic urethane, epoxy, silicone, etc. thermosetting resin or ultraviolet curable resin may also be used.
- a resin having a low photoelastic coefficient such as a polynobornene resin, is also preferable.
- alternating copolymerization of isobutene and N_methylmaleimide A film made of a mixed extrudate of a resin composition containing the unified polymer and an acrylonitrile-styrene copolymer can also be used. Such a film can be manufactured, for example, as described below.
- the above alternating copolymer 100 parts by weight having an N-methylmaleimide content of 50 mol%, and 67 parts by weight of the above copolymer having a tolyl content of 27% by acryl and a styrene content of 73% by weight were used.
- Is melt-kneaded and the pellets are fed to a melt extruder equipped with a T-die to produce a raw film.
- This film is subjected to free-end longitudinal uniaxial stretching under the conditions of a stretching speed of 100 cmZ, a stretching ratio of 1.45 times, and a stretching temperature of 162 ° C.
- a stretched film having a thickness of 49 m can be obtained.
- these transparent protective films may be, for example, saponified by using an aluminum foil or the like.
- a TAC film is preferable from the viewpoints of polarization characteristics and durability, and more preferably a TAC film.
- the surface is a saponified TAC film.
- the transparent protective layer is preferably, for example, not colored.
- the retardation value (Rth) in the film thickness direction represented by the following formula is preferably in the range of 190 nm to 1775 nm, more preferably in the range of 180 nm to +60 nm. Particularly preferably, it is in the range of -70 nm to 1045 nm.
- the coloring (optical coloring) of the polarizing plate caused by the protective film can be sufficiently eliminated.
- d is the thickness of the transparent protective layer
- nx, ny, and nz represent the refractive indices of the X, Y, and Z axes in the transparent protective layer, respectively.
- the X axis is an axis direction indicating the maximum refractive index in the plane of the transparent protective layer
- the Y axis is an axis direction perpendicular to the X axis in the plane
- the Z axis is Indicates the thickness direction perpendicular to the X axis and the Y axis.
- the thickness of the transparent protective layer is not particularly limited, but is, for example, 500 m or less, preferably 1 to 3 OO wm, and more preferably 5 to 5 for the purpose of reducing the thickness of the polarizing plate.
- the range is 300 m.
- the transparent protective layer may be further subjected to, for example, an eighteen-do coating process, an anti-reflection process, a anti-stating process, a process for diffusion, anti-glare, or the like.
- the hard coat treatment is for the purpose of preventing scratches on the surface of the polarizing plate, and forms, for example, a cured film made of a hardening resin and having excellent hardness and slipperiness on the surface of the transparent protective layer. Processing.
- an ultraviolet curable resin such as a silicone-based, urethane-based, acrylic-based, or epoxy-based resin can be used, and the treatment can be performed by a conventionally known method.
- the antireflection treatment is intended to prevent reflection of external light on the polarizing plate surface, It can be performed by forming a conventionally known antireflection film or the like.
- the anti-sticking treatment aims at preventing adhesion between adjacent layers.
- the anti-glare treatment is intended to prevent external interference of the light transmitted through the polarizing plate by reflecting external light on the surface of the polarizing plate.
- a fine particle is formed on the surface of the transparent protective layer by a conventionally known method. This can be achieved by forming a rough structure. Examples of the method of forming such a concavo-convex structure include a method of forming a surface by sandblasting or embossing, and a method of forming the transparent protective layer by blending transparent fine particles with the transparent resin as described above. can give.
- the transparent fine particles include silica, alumina, titania, zirconia, tin oxide, indium oxide, cadmium oxide, antimony oxide, and solid solutions thereof.
- the average particle size of such transparent fine particles is not particularly limited, but is, for example, in the range of 0.5 to 50 im.
- inorganic fine particles having conductivity, organic fine particles composed of a cross-linked or uncross-linked polymer particle, or the like can also be used.
- the blending ratio of the transparent fine particles is not particularly limited, but is generally preferably in the range of 2 to 50 parts by mass, more preferably 5 to 25 parts by mass per 100 parts by mass of the transparent resin as described above. Range.
- the antiglare layer containing the transparent fine particles can be used, for example, as the transparent protective layer itself, or may be formed as a coating layer on the surface of the transparent protective layer. Further, the anti-glare layer may also serve as a diffusion layer for diffusing light transmitted through the polarizing plate to increase the viewing angle.
- the antireflection film, the diffusion layer, the antiglare layer, and the like can be provided on the polarizing plate separately from the transparent protective layer, for example, as an optical layer composed of a sheet or the like provided with these layers. .
- the method of bonding the polarizer and the transparent protective layer is not particularly limited. It can be performed by a known method. Generally, an adhesive or another adhesive is used, and the type can be appropriately determined according to the type of the polarizing film or the transparent protective layer. Specific examples include adhesives and pressure-sensitive adhesives composed of PVA-based, modified PVA-based, and urethane-based polymers. These adhesives are used to improve durability, for example, vinyl alcohol such as boric acid, borax, glutaraldehyde, melamine, oxalic acid, chitin, chitosan, metal salts, alcoholic solvents, etc. A water-soluble crosslinking agent for crosslinking the system polymer may be added.
- a PVA-based adhesive is preferable from the viewpoint of the stability of the bonding treatment and the like.
- the thickness of such an adhesive layer is not particularly limited, but is, for example, 1 nm to 500 nm, preferably 10 nm to 300 nm, and more preferably 20 nm to 100 nm. .
- drying is performed to prevent peeling due to the influence of humidity or heat and to obtain a polarizing plate having excellent light transmittance and degree of polarization.
- a treatment is applied.
- the drying temperature is not particularly limited and can be appropriately determined according to the type of the adhesive or the pressure-sensitive adhesive used.
- the pre-adhesive is a water-soluble adhesive such as the PVA-based, modified PVA-based, or urethane-based adhesive described above, for example, the drying temperature is preferably 60 to 70 ° C, and more preferably 60 to 75 ° C. C, and the drying time is preferably about 1 to 10 minutes.
- the polarizing plate of the present invention preferably further has a pressure-sensitive adhesive layer as the outermost layer, for example, because it can be easily laminated on a liquid crystal cell or the like.
- FIG. 2 shows a cross-sectional view of a polarizing plate having an adhesive layer as described above.
- the polarizing plate 20 includes the polarizing plate 10 and the pressure-sensitive adhesive layer 3 shown in FIG. 1, and the pressure-sensitive adhesive layer 3 is further disposed on the surface of one of the transparent protective layers 2 of the polarizing plate 10. Is placed.
- the pressure-sensitive adhesive layer is formed on the surface of the transparent protective layer by, for example, directly adding a solution or a melt of the pressure-sensitive adhesive to a predetermined surface of the transparent protective layer by a developing method such as casting and coating. This can be performed by a method of forming a pressure-sensitive adhesive layer, or a method of forming a pressure-sensitive adhesive layer on a separator described later and transferring it to a predetermined surface of the transparent protective layer.
- such an adhesive layer may be formed on any one surface of the polarizing plate as shown in FIG. 2, but is not limited thereto, and may be arranged on both surfaces as needed. .
- the pressure-sensitive adhesive layer can be formed by appropriately using a conventionally known pressure-sensitive adhesive such as, for example, an acrylic, silicone, polyester, polyurethane, polyether, or rubber.
- a conventionally known pressure-sensitive adhesive such as, for example, an acrylic, silicone, polyester, polyurethane, polyether, or rubber.
- moisture absorption is necessary in order to prevent foaming and peeling due to moisture absorption, to prevent deterioration of optical characteristics due to differences in thermal expansion, to prevent warpage of liquid crystal cells, and to form high quality and durable liquid crystal display devices.
- an adhesive having a low rate and excellent heat resistance examples include acrylic, silicone, acrylic silicone, polyester and heat-resistant rubber adhesives.
- it may be an adhesive layer or the like containing fine particles and exhibiting light diffusion.
- the surface of the pressure-sensitive adhesive layer provided on the polarizing plate When the surface of the pressure-sensitive adhesive layer provided on the polarizing plate is exposed, the surface may be covered with a separator to prevent contamination or the like until the pressure-sensitive adhesive layer is put to practical use. preferable.
- a release coat using a release agent such as a silicone-based, long-chain alkyl-based, fluorine-based, or molybdenum sulfide is applied to an appropriate thin film such as the transparent protective film, if necessary. It can be formed by a method of providing.
- the thickness of the pressure-sensitive adhesive layer is not particularly limited, but is preferably, for example, 5 to 35 m, more preferably 10 to 25 zm, and particularly preferably 15 to 25 m. By setting such a range, for example, even if the dimensions of the polarizing plate change, the stress generated at that time can also be reduced. Because.
- the polarizing plate of the present invention can be used for forming a liquid crystal cell, a liquid crystal display device, or the like.
- the polarizer may be cut (chip cut), or the polarizer may be cut in advance, and then the transparent protective layer may be bonded.
- a second example of the optical film of the present invention is a laminate including the polarizer of the present invention or the polarizing plate of the first example, and at least one of a polarization conversion element and a retardation film. It is.
- the polarization conversion element is not particularly limited, and examples thereof include those generally used for forming a liquid crystal display device and the like, such as an anisotropic reflection type polarization element and an anisotropic scattering type polarization element.
- These polarization conversion elements may be, for example, a single layer or a laminate of two or more layers. When two or more layers are used, the same kind may be used or different kinds of layers may be used.
- the anisotropic reflection polarizing element is, for example, a composite of a cholesteric liquid crystal layer and a retardation plate, and the retardation plate has the anisotropic reflection polarizer. It is preferable to exhibit a phase difference of 0.2 to 0.3 times the wavelength included in the reflection band. More preferably, it is 0.25 times.
- a left-handed or right-handed circularly polarized light such as an alignment film of a cholesteric liquid crystal polymer or a film in which the alignment liquid crystal layer is supported on a film substrate. It is preferable to exhibit a property of reflecting and transmitting other light.
- an anisotropic reflective polarizing element for example, PCF series manufactured by Nitto Denko and the like can be used.
- the wavelength may be any wavelength as long as it is included in the reflection band of the anisotropic reflection polarizer.
- the cholesteric liquid crystal layer is, for example, a multilayer thin film of a dielectric, As in the case of a multilayer laminate of thin film films having different refractive index anisotropies, it may transmit linearly polarized light having a predetermined polarization axis and reflect other light.
- an anisotropic reflective polarizing element for example, the trade name DBEF series manufactured by 3M can be used.
- a reflection-type grid polarizer is also preferable.
- MicRoWires (trade name) manufactured by Moxtek can be used.
- a third example of the optical film of the present invention includes, for example, the polarizer of the present invention, the polarizing plate of the first example, or the laminate of the second example, and various optical layers.
- Various polarizing plates which are laminates are exemplified.
- optical layer examples include, but are not particularly limited to, a retardation plate including a ⁇ plate such as a reflector, a semi-transmissive reflector, a ⁇ wavelength plate, and a 1Z 4 wavelength plate, as shown below,
- a retardation plate including a ⁇ plate such as a reflector, a semi-transmissive reflector, a ⁇ wavelength plate, and a 1Z 4 wavelength plate
- optical layers used for forming liquid crystal display devices and the like such as viewing angle compensation films and brightness enhancement films. These optical layers may be used alone or in combination of two or more.
- the polarizing plate including such an optical layer include a reflective polarizing plate, a transflective polarizing plate, an elliptical polarizing plate, a circular polarizing plate, a polarizing plate on which a viewing angle compensation film and a brightness enhancement film are laminated, and the like. preferable.
- the reflective polarizing plate is, for example, a polarizing plate further laminated on the polarizing plate of the first example as described above, and the transflective polarizing plate is further provided with a semi-transmissive reflecting plate on the polarizing plate. It is laminated.
- the reflection type polarizing plate is usually arranged on the back side of a liquid crystal cell, and can be used for a liquid crystal display device (reflection type liquid crystal display device) for reflecting incident light from a viewing side (display side) for display. .
- a reflective polarizing plate has advantages, for example, in that a light source such as a backlight can be omitted, and thus the liquid crystal display device can be made thinner.
- the reflective polarizing plate can be manufactured by a conventionally known method such as a method of forming a reflective plate made of metal or the like on one surface of the polarizing plate after the heat treatment. Specifically, for example, one surface (exposed surface) of the transparent protective layer in the polarizing plate is subjected to a mat treatment as necessary, and a metal foil made of a reflective metal such as aluminum is deposited on the surface to reflect a vapor-deposited film.
- a reflection type polarizing plate formed as a plate is exemplified.
- a reflective polarizing plate and the like in which a reflective plate reflecting the fine uneven structure is formed on a transparent protective layer having a fine uneven structure on the surface by incorporating fine particles in various transparent resins as described above, are also available.
- a reflector having a fine uneven structure on the surface has the advantage that, for example, the incident light is diffused by irregular reflection, the directivity can be prevented from glare, and uneven brightness can be suppressed.
- Such a reflection plate is directly provided on the uneven surface of the transparent protective layer by a conventionally known method such as a vacuum evaporation method, an ion plating method, a sputtering method, or a plating method. ⁇ It can be formed as a metal deposition film.
- a reflective sheet such as the transparent protective film provided with a reflective layer on an appropriate film, such as the transparent protective film, is used as the reflective plate. May be used. Since the reflection layer of the reflection plate is usually made of metal, for example, it is necessary to prevent a decrease in reflectance due to oxidation, and to maintain the initial reflectance for a long period of time, and to avoid separately forming a transparent protective layer. From the usage, the reflection surface of the reflection layer Is preferably covered with the film or the polarizing plate.
- the transflective polarizing plate is a transflective polarizing plate having a transflective reflecting plate instead of the reflecting plate.
- the semi-transmissive reflection plate include a half mirror that reflects light on a reflection layer and transmits light.
- the semi-transmissive polarizing plate is usually provided on the back side of a liquid crystal cell.
- a liquid crystal display device or the like When a liquid crystal display device or the like is used in a relatively bright atmosphere, it reflects incident light from the viewing side (display side) to form an image.
- the liquid crystal display device In a relatively dark atmosphere, the liquid crystal display device can be used for a liquid crystal display device or the like that displays an image using a built-in light source such as a backlight built in the pack side of the transflective polarizing plate. That is, the transflective polarizing plate can save energy for use of a light source such as a backlight in a bright atmosphere, and can be used with the built-in light source even in a relatively dark atmosphere. It is useful for forming liquid crystal display devices.
- a retardation plate or a ⁇ plate is further laminated on the polarizing plate of the first example described above.
- the elliptically polarizing plate compensates (prevents) coloring (blue or yellow) caused by birefringence of a liquid crystal layer of a super twisted nematic (STN) type liquid crystal display device, for example, to provide a monochrome display without the coloring. It is used effectively in cases such as Further, an elliptically polarizing plate having a controlled three-dimensional refractive index is preferable because, for example, coloring that occurs when a screen of a liquid crystal display device is viewed from an oblique direction can be compensated (prevented).
- the circularly polarizing plate is effective when, for example, an image is displayed in a single color, when adjusting the color tone of an image of a reflective liquid crystal display device, and has a function of preventing reflection.
- the retardation plate converts linearly polarized light into elliptically polarized light or circularly polarized light, It is used to convert circularly polarized light or circularly polarized light to linearly polarized light, or to polarize the direction of linearly polarized light.
- a 1Z 4 wavelength plate also referred to as “ ⁇ 4 plate”
- a half-wave plate also referred to as “ ⁇ / 2 plate” is usually used.
- Examples of the material of the retardation plate include birefringent films obtained by stretching a polymer film such as polycarbonate, PVA, polystyrene, polymethyl methacrylate, polypropylene and other polyolefins, polyarylates, polyamides, and polynorbornene, and liquid crystal polymers. Oriented films, laminates in which an oriented layer of liquid crystal polymer is supported by a film, and the like can be given.
- the types of the retardation plate include, for example, various wavelength plates such as the above 1/2 and 1/4, and those for the purpose of compensating coloring due to birefringence of a liquid crystal layer and compensating a viewing angle such as a widening of a viewing angle.
- a film having a retardation according to the purpose may be used, or an obliquely oriented film having a controlled refractive index in the thickness direction may be used.
- a laminate in which two or more retardation plates are laminated and optical characteristics such as retardation are controlled may be used.
- a method of applying a heat-shrinkable film to a polymer film and subjecting the polymer film to a stretching treatment or a shrinkage treatment under the action of the shrinkage force by heating It can be obtained by an oblique orientation method or the like.
- the viewing angle compensation film for example, the image of the liquid crystal display device is not perpendicular to the screen, even when viewed from a slightly oblique direction, the image is relatively clear It is a film to widen the viewing angle so that it can be seen.
- a viewing angle compensation film for example, a film obtained by coating a discotic liquid crystal on a triacetyl cellulose film or the like, or a retardation plate is used.
- a normal retardation plate for example, a birefringent polymer film uniaxially stretched in the plane direction is used, whereas as the viewing angle compensation film, for example, biaxially in the plane direction is used.
- Two-way stretching such as a stretched birefringent polymer film or an obliquely oriented polymer film with a controlled refractive index in the thickness direction that is uniaxially stretched in the plane direction and also stretched in the thickness direction
- a retardation plate such as a film
- the inclined alignment film include, for example, a heat-shrinkable film adhered to a polymer film, and the polymer film is subjected to a stretching treatment or a shrinking treatment under the action of the shrinking force due to heating. And the like.
- the raw material for the polymer film the same material as the polymer material for the retardation plate, which has been previously extended, can be used.
- This polarizing plate is usually used by being arranged on the back side of a liquid crystal cell.
- the brightness enhancement film reflects, for example, a backlight of a liquid crystal display device or the like, reflection of light from the back side thereof, etc., when natural light enters, reflects linearly polarized light of a predetermined polarization axis or circularly polarized light of a predetermined direction, and other light is It shows the transmission characteristics. Light from a light source such as a backlight is incident to obtain transmitted light in a predetermined polarization state, and light other than the predetermined polarization state is reflected without transmitting.
- the light reflected on the brightness enhancement film surface is further inverted via a reflection plate or the like provided on the rear side thereof, re-incident on the brightness enhancement film, and part or all of the light is transmitted as light of a predetermined polarization state.
- a polarizing film polarizer
- the brightness enhancement film reflects light having a polarization direction that is absorbed by the polarizer without being incident on the polarizer, but reflects the light once on the brightness enhancement film, and is provided on the rear side thereof. Inversion through a reflector or the like and re-incident on the brightness enhancement film are repeated. Then, only the polarized light having a polarization direction in which the light reflected and inverted between the two is polarized so as to be able to pass through the polarizer is transmitted and supplied to the polarizer. This light can be efficiently used for displaying images on the liquid crystal display device, and the screen can be brightened.
- a diffusion plate may be provided between the brightness enhancement film and the reflection layer or the like.
- the light in the polarization state reflected by the brightness enhancement film goes to the reflection layer, but the diffusion plate installed diffuses the passing light uniformly, and at the same time, eliminates the polarization state and becomes unpolarized. State. In other words, it returns to the state of natural light.
- the light in the non-polarized state that is, the light in the natural light state is repeatedly directed to the reflection layer and the like, reflected through the reflection layer, passed through the diffusion plate again, and re-enters the brightness enhancement film.
- the diffuser plate appropriately increases the number of repetitions of reflection of the first incident light, and provides a uniform bright display screen in combination with the diffuser function of the diffuser plate.
- the brightness enhancement film is not particularly limited, and, for example, transmits linearly polarized light having a predetermined polarization axis, such as a multilayer thin film of a dielectric or a multilayer laminate of thin films having different refractive index anisotropies. Other light reflecting characteristics can be used. Specifically, for example, a product name D-BEF manufactured by 3M Company can be used. Also, such as a cholesteric liquid crystal layer, particularly an oriented film of a cholesteric liquid crystal polymer, or a film in which the oriented liquid crystal layer is supported on a film substrate, reflects one of the left and right circularly polarized light and transmits other light. It may show characteristics. As such a film, for example, Nitto Denko Corporation's trade name “PCF350”, Merck Corporation's trade name Transma a, and the like can be used.
- a cholesteric liquid crystal layer particularly an oriented film of a cholesteric liquid crystal polymer, or a film in which the
- a brightness enhancement film of a type that transmits linearly polarized light having a predetermined polarization axis for example, the transmitted light is directly incident on the polarization plate with the polarization axis aligned, thereby suppressing absorption loss by the polarization plate.
- a brightness enhancement film that transmits circularly polarized light such as a cholesteric liquid crystal layer, can be directly incident on the polarizer.
- the transmitted circularly polarized light is converted into a phase difference. It is preferable that the light is linearly polarized through a plate and is incident on the polarizing plate. Note that, for example, by using a quarter-wave plate as the retardation plate, circularly polarized light can be converted to linearly polarized light.
- a retardation plate that functions as a 1/4 wavelength plate in a wide wavelength range such as a visible light region is, for example, a retardation layer that functions as a 1/4 wavelength plate for monochromatic light such as light with a wavelength of 550 nm. It can be obtained by laminating a phase difference layer exhibiting other phase difference characteristics (for example, a phase difference layer functioning as a 1Z2 wavelength plate). Therefore, as a retardation plate disposed between the polarizing plate and the brightness enhancement film,
- the cholesteric liquid crystal layer can also have a laminated structure in which two or three or more layers are laminated by combining those having different reflection wavelengths.
- a polarizing plate that reflects circularly polarized light in a wide wavelength range such as a visible light region can be obtained, and based on that, transmitted circularly polarized light in a wide wavelength range can be obtained.
- the various polarizing plates in the third example as described above may be, for example, an optical film obtained by laminating the polarizing plate and two or three or more optical layers.
- a reflection type elliptically polarizing plate or a semi-transmission type elliptically polarizing plate obtained by combining the above-mentioned reflection type polarizing plate or semi-transmission type polarizing plate with a retardation plate can be used.
- an optical film in which two or more optical layers are laminated can be formed, for example, by a method of sequentially laminating in the process of manufacturing a liquid crystal display device or the like.
- a method of sequentially laminating in the process of manufacturing a liquid crystal display device or the like there is an advantage that, for example, the stability of quality and the workability of assembling are excellent, and the manufacturing efficiency of a liquid crystal display device or the like can be improved.
- Various adhesive means such as an adhesive layer can be used.
- the layers such as the polarizing film, the transparent protective layer, the optical layer, and the pressure-sensitive adhesive layer which form the optical film of the present invention as described above include, for example, salicylic acid ester compounds, benzophenone compounds, benzotriazole compounds, A compound having an ultraviolet absorbing ability by appropriately treating with an ultraviolet absorbing agent such as a cyanoacrylate compound or a nickel complex compound may be used.
- the liquid crystal panel of the present invention includes at least one of the polarizer and the optical film of the present invention (hereinafter, also referred to as “optical film”). This is arranged on at least one surface of the liquid crystal cell.
- the type of the liquid crystal cell is not particularly limited, and a conventionally known liquid crystal cell can be appropriately used.
- the polarizer and the like of the present invention are useful for a liquid crystal display device in which polarized light is incident on the liquid crystal cell for display. Therefore, among them, for example, a liquid crystal cell using a TN (Twisted Nematic) liquid crystal or an STN (Super Twisted Nematic) liquid crystal is preferable.
- IPS In-Plane Switching
- VA Vertical
- ⁇ CB Optically Compensated Birefringence
- guest-host type liquid crystal in which dichroic dye is dispersed in liquid crystal or liquid crystal cell using ferroelectric liquid crystal .
- the driving method of the liquid crystal is not particularly limited.
- the optical film such as the polarizing plate may be disposed on only one surface of the liquid crystal cell, or may be disposed on both surfaces.
- the types of the optical films may be the same or different.
- polarizing plates and optical members are provided on both sides of the liquid crystal cell, they may be the same or different.
- ordinary components such as a prism array sheet, a lens array sheet, and a light diffusing plate may be provided at an appropriate position, and one or more of these components may be arranged.
- FIG. 3 to 5 show examples of a liquid crystal panel on which the optical film of the present invention is arranged. These figures are cross-sectional views showing the state of lamination of a liquid crystal cell and an optical film, and are hatched to distinguish components. In each drawing, the same parts are denoted by the same reference numerals. Note that the liquid crystal panel of the present invention is not limited to these. .
- the liquid crystal panel in FIG. 3 has a liquid crystal cell 12 and a polarizing plate 11, and the polarizing plates 11 are arranged on both sides of the liquid crystal cell 12, respectively.
- the liquid crystal The cell structure (not shown) is not particularly limited, and is generally a structure in which liquid crystal is held between an array substrate and a filter substrate.
- the liquid crystal panel in FIG. 4 has a liquid crystal cell 12, a polarizing plate 11 and a retardation plate 13, and the polarizing plate 11 is provided on both sides of the liquid crystal cell 12 via a retardation plate 13 respectively. It is laminated.
- the retardation plate 13 and the polarizing plate 11 may be disposed on both sides of the liquid crystal cell 12 as an integrated optical film of the present invention.
- the liquid crystal panel in FIG. 5A includes a liquid crystal cell 12, a polarizing plate 11 and a polarization conversion element 14, and the polarizing plates 11 are laminated on both sides of the liquid crystal cell 12, respectively.
- the polarization conversion element 14 is further laminated on one side of the substrate.
- an element as described above can be used as the polarization conversion element 14, as shown in FIG. 1B.
- a composite of a 1Z4 wavelength plate 15 and a cholesteric liquid crystal 16 An anisotropic multiple thin film reflective polarizing element 17 as shown in FIG.
- the polarizing plate 11 and the polarization conversion element 14 may be disposed on one surface of the liquid crystal cell 12 as an integrated optical film of the present invention.
- a liquid crystal display device of the present invention is a liquid crystal display device including a liquid crystal panel, wherein the liquid crystal panel is the liquid crystal panel of the present invention.
- This liquid crystal display device may further include a light source.
- the light source is not particularly limited, but is preferably, for example, a planar light source that emits polarized light, for example, because light energy can be used effectively.
- an electroluminescent (EL) display device of the present invention is a display device having at least one of the polarizer of the present invention and the optical film of the present invention. This EL device may be either an organic EL or an inorganic EL.
- an optical film such as a polarizer or a polarizing plate together with a ⁇ / 4 plate in an EL display device to prevent reflection from an electrode in a black state.
- the polarizer and the optical film of the present invention are particularly suitable when the EL layer emits linearly polarized light, circularly polarized light, or elliptically polarized light, or emits natural light in the frontal direction. This is very useful when the emitted light in the oblique direction is partially polarized.
- a general organic EL display device will be described.
- the organic EL display device generally has a light-emitting body (organic EL light-emitting body) in which a transparent electrode, an organic light-emitting layer, and a metal electrode are laminated in this order on a transparent substrate.
- the organic light emitting layer is a laminate of various organic thin films, for example, a laminate of a hole injection layer made of a triphenylamine derivative or the like and a light emitting layer made of a fluorescent organic solid such as anthracene or the like.
- Various combinations such as a laminated body of a layer and an electron injection layer made of a perylene derivative, and a laminated body of the hole injection layer, the light emitting layer, and the electron injection layer are exemplified.
- an organic EL display device by applying a voltage to the anode and the cathode, holes and electrons are injected into the organic light emitting layer, and the holes and electrons are recombined.
- the energy generated by the phosphor excites the phosphor and emits light when the excited phosphor returns to the ground state.
- the mechanism of the recombination of holes and electrons is the same as that of a general diode, and the current and emission intensity show strong nonlinearity with rectification with respect to the applied voltage.
- at least one of the electrodes needs to be transparent in order to extract light emitted from the organic light emitting layer. Therefore, a transparent conductor such as indium tin oxide (ITO) is usually used.
- ITO indium tin oxide
- the formed transparent electrode is used as an anode.
- a metal electrode such as Mg-Ag or Al-Li is used. Is used.
- the organic light emitting layer is formed of, for example, an extremely thin film having a thickness of about 10 nm. This is because even in the organic light emitting layer, light is transmitted almost completely, similarly to the transparent electrode. As a result, when the light is not emitted, the light that enters from the surface of the transparent substrate, passes through the transparent electrode and the organic light emitting layer, and is reflected by the metal electrode exits to the surface of the transparent substrate again. Therefore, when viewed from the outside, the display surface of the organic EL display device looks like a mirror surface.
- the organic EL display device of the present invention is, for example, an organic EL display device including the organic EL light emitting device, which includes a transparent electrode on a front surface side of the organic light emitting layer and a metal electrode on a back surface side of the organic light emitting layer.
- the optical film (such as a polarizing plate) of the present invention is disposed on the surface of the transparent electrode, and a ⁇ / 4 plate is preferably disposed between the polarizing plate and the EL element.
- a retardation plate is further disposed between the transparent electrode and the optical film.
- the retardation plate and the optical film have a function of, for example, polarizing light incident from the outside and reflected by the metal electrode. Must be visible from Has the effect.
- a 1/4 wavelength plate is used as the phase difference plate and the angle between the polarization direction of the polarizing plate and the phase difference plate is adjusted to / 4, the mirror surface of the metal electrode is completely shielded. can do. That is, only the linearly polarized light component of the external light incident on the organic EL display device is transmitted by the polarizing plate.
- the linearly polarized light is generally converted into elliptically polarized light by the retardation plate.
- the retardation plate is a 1Z4 wavelength plate and the angle is ⁇ Z4, the linearly polarized light is circularly polarized light.
- This circularly polarized light passes through, for example, a transparent substrate, a transparent electrode, and an organic thin film, is reflected by a metal electrode, passes through the organic thin film, the transparent electrode, and the transparent substrate again, and is straightened by the retardation plate. It becomes polarized light. Since the linearly polarized light is orthogonal to the polarization direction of the polarizing plate, the linearly polarized light cannot pass through the polarizing plate. As a result, as described above, the mirror surface of the metal electrode can be completely shielded. is there.
- liquid crystal display device and the in-house manufacturing method for an EL display device according to the present invention provide the polarizer according to the present invention, which comprises a surface protective film on the display surface side and an adhesive layer and a release layer on the opposite surface. And a step of attaching at least one of the optical films of the present invention to the display device immediately after chip cutting.
- the polarizer or the optical film of the present invention is masked on a portion that does not satisfy the above condition (1), and immediately after punching, is bonded to a liquid crystal panel or an EL display element.
- Various display devices can be manufactured.
- polarized light Since the steps from punching, sorting, and laminating the chip and optical film can be performed consistently, and the inspection time can be simplified, manufacturing can be simplified and costs can be reduced. it can.
- in-house refers to an integrated line from punching a roll of a polarizing plate, inspecting it, and bonding it to an LCD.
- the PVA film is subjected to a swelling treatment, a dyeing treatment, a cross-linking treatment, a stretching treatment, and a water washing treatment to produce a polarizer. Produced. Then, the performances of the polarizer and the polarizer were evaluated.
- the PVA film include a PVA film having a degree of polymerization of 2400 (manufactured by Kuraray Co., Ltd .; trade name: VF-PS # 7500; width: 600 mm) and a PVA film having a degree of polymerization of 2600 (manufactured by Nippon Gohsei; trade name: OPL) M-750; width: 600 mm).
- the type of PVA film used in each of the examples and comparative examples is shown in Table 1 below according to the degree of polymerization. Table 1 also shows the thickness and thickness displacement of the PVA film (raw material).
- the PVA film was subjected to a swelling treatment under the conditions shown in Table 1 below. Specifically, the PVA film was immersed in a water bath (swelling bath) and stretched. Table 1 below shows the immersion time, swelling bath temperature, PVA film before swelling ( The drawing ratio is shown with respect to the length of the raw material. In addition, a guide roll was used in order to improve drainage in the swelling bath (the same applies hereinafter).
- the PVA film was pulled out of the swelling bath, immersed in an aqueous solution (dying bath) containing 0.03% by weight of iodine, and further stretched.
- Table 1 shows the immersion time, the temperature of the dyeing bath, and the draw ratio for the length of the raw material.
- the PVA film was pulled out of the dyeing bath, immersed in an aqueous solution containing boric acid and KI (crosslinking bath), and further stretched.
- Table 1 shows the immersion time, the temperature of the crosslinking bath, the stretching ratio with respect to the length of the raw fabric, the concentration of boric acid and the concentration of KI in the dyeing bath.
- Table 1 shows the immersion time in the crosslinking bath.
- the PVA film was pulled out of the crosslinking bath, immersed in an aqueous solution containing boric acid and KI (stretching bath), and further stretched.
- Table 1 shows the immersion time, the temperature of the immersion bath, the stretching ratio with respect to the length of the raw fabric, the concentration of boric acid and the concentration of KI in the stretching bath.
- Table 1 shows the immersion time in the stretching bath (time for the stretching process).
- the PVA film was pulled out of the stretching bath, immersed in a KI aqueous solution (a washing bath), and then washed with water.
- Table 1 shows the K I concentration in the washing bath and the temperature of the washing bath.
- the water-washed PVA film was dried at 25 ° C. for 3 minutes to obtain a polarizer.
- the results are shown in Table 1.
- a TAC film of KC4UVX2MW (manufactured by Konica Film) was previously immersed in a 5% by weight aqueous solution of NAOH at 40 ° C for 2 minutes, washed with pure water at 30 ° C for 1 minute, and then washed with 100 ° C. C for 2 minutes to obtain a saponified protective film (thickness 40 Was prepared.
- the phase difference of this protective film using a phase difference meter (trade name: KOBRA21ADH, manufactured by Oji Scientific Instruments), the in-plane retardation was 1 nm and the thickness direction retardation was 27 nm. (Measuring wavelength 550 nm).
- the protective film was attached to both surfaces of the polarizer with a 3% by weight aqueous solution of PVA and dried (at 65 ° C. for 5 minutes) to produce a polarizing plate.
- the in-plane retardation of the polarizing plate was measured using a brand name KOBRA-31PR (manufactured by Oji Scientific Instruments) (measuring wavelength lOOOOnm). Specifically, for a polarizing plate having a length of 25 Omm and a width of 20 Omm, a total of 122,76 points were measured every 2 mm in the plane. Table 2 shows these results as the range of phase difference fluctuation of the polarizing plate.
- the polarizing plates obtained in Examples and Comparative Examples were cut into a length of 25 cm and a width of 20 cm each, and bonded to the surface (light source side) of a high-contrast type IPS liquid crystal cell via an adhesive. On the other surface (viewing side) of the liquid crystal cell, SEG1425DU (trade name, manufactured by Nitto Denko) was bonded. Profit The obtained liquid crystal panel was placed on various backlights (A to D) to be described later such that the polarizing plate on the light source side (the prepared polarizing plate) was on the lower side.
- FIG. 6 is a cross-sectional view schematically showing the backlight A.
- the pack light 6 is provided with a cold cathode tube 26 and a lamp house 27 on a wedge-shaped light guide plate 22 having a printed back surface, a diffusion plate 21 on the upper surface, and a diffuser plate 21 on the lower surface. Diffusion panels 23 were arranged respectively.
- FIG. 7 is a cross-sectional view schematically showing the pack light B.
- this pack light 7 has a laminated body of a cholesteric layer and a ⁇ 4 plate layer arranged on the backlight 6 shown in FIG.
- the laminate was arranged such that the cholesteric surface (16) was on the backlight 6 side and the ⁇ 4 plate (15) was on the viewing side.
- the transmitted light amount is maximized.
- As the laminated body of the cholesteric layer and the ⁇ 4 plate layer a laminate obtained by removing only the polarizing plate portion from PCF400 TEG (trade name, manufactured by Nitto Denko Corporation) was used.
- FIG. 8 is a cross-sectional view schematically showing the backlight C.
- the backlight 8 has an anisotropic multiple thin-film reflective polarizer (trade name: DBEF; manufactured by SLEEM) 17 disposed on the backlight 6 shown in FIG.
- DBEF anisotropic multiple thin-film reflective polarizer
- FIG. 9 (A) is a cross-sectional view schematically showing a backlight D
- FIG. 9 (B) is a view schematically showing a partial outline of the above (A).
- the backlight 9 includes a wedge-shaped light guide plate 25 having a prism formed on a light exit surface, a cold cathode tube 26 and a lamp house 27, and a lower surface of the light guide plate 25.
- the prism sheet 24 was arranged so that its prism surface faced the prism surface of the light guide plate 25, as shown in a partially enlarged view (B) of FIG.
- a diffusion plate 21 was further disposed on the upper surface of the prism sheet 24.
- Example 5 1270 -5.2 to 5.6 8cm 62 dishes 44.0 99.97 -1.3 3.3 -2.2 6.0 0.4 -2.2 ⁇
- Example 6 1010-1080 -4.3 to 4.99cm 56nm 44.0 99.97 -1.4 3.4-2.1 6.2 0.3 -2.3 ⁇
- Example 7 strokes ⁇ 1120 -4.7-4.6 10cm 43 plates 44.0 99.97 -1.3 3.3 -2.2 6.1 0.3-2.1
- the cost of the display device can be reduced, and the management of the manufacturing process is easy, so that the industrial value is great.
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Description
Claims
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
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US10/522,187 US20060098137A1 (en) | 2002-07-24 | 2003-07-24 | Polarizer, optical film using it, image display unit using them |
KR1020127014356A KR101348469B1 (ko) | 2002-07-24 | 2003-07-24 | 편광자, 그것을 사용한 광학 필름, 그것들을 사용한 화상 표시 장치 |
US12/230,372 US8698981B2 (en) | 2002-07-24 | 2008-08-28 | Polarizer, optical film using the same, and image display device using the same |
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US12/230,372 Continuation US8698981B2 (en) | 2002-07-24 | 2008-08-28 | Polarizer, optical film using the same, and image display device using the same |
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WO2004019086A1 true WO2004019086A1 (ja) | 2004-03-04 |
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US (2) | US20060098137A1 (ja) |
JP (1) | JP2010152374A (ja) |
KR (4) | KR20090008452A (ja) |
CN (2) | CN1672069A (ja) |
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
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EP1598878A2 (en) * | 2004-05-17 | 2005-11-23 | Lg Electronics Inc. | Organic EL display |
CN100417957C (zh) * | 2005-08-02 | 2008-09-10 | 新和Opla株式会社 | 有机发光二极管显示器用的染料系圆偏光片 |
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Also Published As
Publication number | Publication date |
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KR20120070618A (ko) | 2012-06-29 |
US20090002608A1 (en) | 2009-01-01 |
US8698981B2 (en) | 2014-04-15 |
KR101348469B1 (ko) | 2014-01-07 |
KR20090008452A (ko) | 2009-01-21 |
CN101900851A (zh) | 2010-12-01 |
KR20050030210A (ko) | 2005-03-29 |
US20060098137A1 (en) | 2006-05-11 |
JP2010152374A (ja) | 2010-07-08 |
KR20090008453A (ko) | 2009-01-21 |
TW200401909A (en) | 2004-02-01 |
CN1672069A (zh) | 2005-09-21 |
TWI266907B (en) | 2006-11-21 |
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