TWI868174B - Optical laminate - Google Patents
Optical laminate Download PDFInfo
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- TWI868174B TWI868174B TW109122441A TW109122441A TWI868174B TW I868174 B TWI868174 B TW I868174B TW 109122441 A TW109122441 A TW 109122441A TW 109122441 A TW109122441 A TW 109122441A TW I868174 B TWI868174 B TW I868174B
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- surface protection
- protection film
- polarizing plate
- thickness
- adhesive layer
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- 230000003287 optical effect Effects 0.000 title claims abstract description 39
- 238000000926 separation method Methods 0.000 claims abstract description 43
- 239000012790 adhesive layer Substances 0.000 claims abstract description 34
- 229920005989 resin Polymers 0.000 claims description 67
- 239000011347 resin Substances 0.000 claims description 67
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 50
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 50
- 229910052740 iodine Inorganic materials 0.000 claims description 25
- 239000011630 iodine Substances 0.000 claims description 25
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 23
- 230000005540 biological transmission Effects 0.000 abstract 1
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 24
- 238000000034 method Methods 0.000 description 20
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- 238000004043 dyeing Methods 0.000 description 18
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- 239000007864 aqueous solution Substances 0.000 description 15
- 239000011241 protective layer Substances 0.000 description 14
- -1 iodine ions Chemical class 0.000 description 12
- 239000007788 liquid Substances 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- 238000004132 cross linking Methods 0.000 description 10
- 238000010438 heat treatment Methods 0.000 description 9
- 239000010410 layer Substances 0.000 description 9
- 239000000126 substance Substances 0.000 description 9
- 230000008961 swelling Effects 0.000 description 9
- 239000004925 Acrylic resin Substances 0.000 description 8
- 229920000178 Acrylic resin Polymers 0.000 description 8
- 230000000052 comparative effect Effects 0.000 description 8
- 238000010521 absorption reaction Methods 0.000 description 7
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 7
- 239000004327 boric acid Substances 0.000 description 7
- 150000001639 boron compounds Chemical class 0.000 description 7
- 229920000139 polyethylene terephthalate Polymers 0.000 description 7
- 239000005020 polyethylene terephthalate Substances 0.000 description 7
- 239000000853 adhesive Substances 0.000 description 6
- 230000001070 adhesive effect Effects 0.000 description 6
- 238000007127 saponification reaction Methods 0.000 description 6
- 238000002834 transmittance Methods 0.000 description 6
- 238000005406 washing Methods 0.000 description 6
- 238000004140 cleaning Methods 0.000 description 5
- 150000002148 esters Chemical class 0.000 description 5
- 238000007654 immersion Methods 0.000 description 5
- 150000002500 ions Chemical class 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 238000011156 evaluation Methods 0.000 description 4
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- DKNPRRRKHAEUMW-UHFFFAOYSA-N Iodine aqueous Chemical compound [K+].I[I-]I DKNPRRRKHAEUMW-UHFFFAOYSA-N 0.000 description 3
- 239000004743 Polypropylene Substances 0.000 description 3
- 229920006026 co-polymeric resin Polymers 0.000 description 3
- 150000001925 cycloalkenes Chemical class 0.000 description 3
- 230000032798 delamination Effects 0.000 description 3
- 150000004694 iodide salts Chemical class 0.000 description 3
- 239000004973 liquid crystal related substance Substances 0.000 description 3
- JFNLZVQOOSMTJK-KNVOCYPGSA-N norbornene Chemical compound C1[C@@H]2CC[C@H]1C=C2 JFNLZVQOOSMTJK-KNVOCYPGSA-N 0.000 description 3
- KNCYXPMJDCCGSJ-UHFFFAOYSA-N piperidine-2,6-dione Chemical group O=C1CCCC(=O)N1 KNCYXPMJDCCGSJ-UHFFFAOYSA-N 0.000 description 3
- 230000010287 polarization Effects 0.000 description 3
- 229920006122 polyamide resin Polymers 0.000 description 3
- 229920005668 polycarbonate resin Polymers 0.000 description 3
- 239000004431 polycarbonate resin Substances 0.000 description 3
- 229920005672 polyolefin resin Polymers 0.000 description 3
- 229920001155 polypropylene Polymers 0.000 description 3
- 230000001681 protective effect Effects 0.000 description 3
- FVAUCKIRQBBSSJ-UHFFFAOYSA-M sodium iodide Chemical compound [Na+].[I-] FVAUCKIRQBBSSJ-UHFFFAOYSA-M 0.000 description 3
- 229920000219 Ethylene vinyl alcohol Polymers 0.000 description 2
- 101001121408 Homo sapiens L-amino-acid oxidase Proteins 0.000 description 2
- 102100026388 L-amino-acid oxidase Human genes 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 125000002339 acetoacetyl group Chemical group O=C([*])C([H])([H])C(=O)C([H])([H])[H] 0.000 description 2
- 239000002313 adhesive film Substances 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 239000003431 cross linking reagent Substances 0.000 description 2
- 238000004049 embossing Methods 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 238000010030 laminating Methods 0.000 description 2
- HSZCZNFXUDYRKD-UHFFFAOYSA-M lithium iodide Chemical compound [Li+].[I-] HSZCZNFXUDYRKD-UHFFFAOYSA-M 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 229920005992 thermoplastic resin Polymers 0.000 description 2
- 230000037303 wrinkles Effects 0.000 description 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
- UAYWVJHJZHQCIE-UHFFFAOYSA-L zinc iodide Chemical compound I[Zn]I UAYWVJHJZHQCIE-UHFFFAOYSA-L 0.000 description 2
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- UNMYWSMUMWPJLR-UHFFFAOYSA-L Calcium iodide Chemical compound [Ca+2].[I-].[I-] UNMYWSMUMWPJLR-UHFFFAOYSA-L 0.000 description 1
- 229920001747 Cellulose diacetate Polymers 0.000 description 1
- 229920002284 Cellulose triacetate Polymers 0.000 description 1
- 239000004593 Epoxy Chemical class 0.000 description 1
- 239000006087 Silane Coupling Agent Substances 0.000 description 1
- 238000002441 X-ray diffraction Methods 0.000 description 1
- 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 1
- 230000032900 absorption of visible light Effects 0.000 description 1
- 239000003522 acrylic cement Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 238000007605 air drying Methods 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- CECABOMBVQNBEC-UHFFFAOYSA-K aluminium iodide Chemical compound I[Al](I)I CECABOMBVQNBEC-UHFFFAOYSA-K 0.000 description 1
- 238000004458 analytical method Methods 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
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000007767 bonding agent Substances 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 229910001640 calcium iodide Inorganic materials 0.000 description 1
- 229940046413 calcium iodide Drugs 0.000 description 1
- 238000011088 calibration curve Methods 0.000 description 1
- 239000012461 cellulose resin Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- GBRBMTNGQBKBQE-UHFFFAOYSA-L copper;diiodide Chemical compound I[Cu]I GBRBMTNGQBKBQE-UHFFFAOYSA-L 0.000 description 1
- 238000003851 corona treatment Methods 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-M iodide Chemical compound [I-] XMBWDFGMSWQBCA-UHFFFAOYSA-M 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 238000003475 lamination Methods 0.000 description 1
- 239000000113 methacrylic resin Substances 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- QQVIHTHCMHWDBS-UHFFFAOYSA-N perisophthalic acid Natural products OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 235000009518 sodium iodide Nutrition 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 239000002335 surface treatment layer Substances 0.000 description 1
- 239000004094 surface-active agent Substances 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
- WRTMQOHKMFDUKX-UHFFFAOYSA-N triiodide Chemical compound I[I-]I WRTMQOHKMFDUKX-UHFFFAOYSA-N 0.000 description 1
- 229940006158 triiodide ion Drugs 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
- 150000003752 zinc compounds Chemical class 0.000 description 1
- NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 description 1
- 229960001763 zinc sulfate Drugs 0.000 description 1
- 229910000368 zinc sulfate Inorganic materials 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
- 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
- G02B5/3041—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 comprising multiple thin layers, e.g. multilayer stacks
- G02B5/305—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 comprising multiple thin layers, e.g. multilayer stacks including organic materials, e.g. polymeric layers
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J201/00—Adhesives based on unspecified macromolecular compounds
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J7/00—Adhesives in the form of films or foils
- C09J7/30—Adhesives in the form of films or foils characterised by the adhesive composition
- C09J7/38—Pressure-sensitive adhesives [PSA]
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J7/00—Adhesives in the form of films or foils
- C09J7/40—Adhesives in the form of films or foils characterised by release liners
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B1/00—Optical elements characterised by the material of which they are made; Optical coatings for optical elements
- G02B1/10—Optical coatings produced by application to, or surface treatment of, optical elements
- G02B1/14—Protective coatings, e.g. hard coatings
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B5/00—Optical elements other than lenses
- G02B5/30—Polarising elements
-
- G—PHYSICS
- G02—OPTICS
- 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
- G02F1/133528—Polarisers
Landscapes
- Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Nonlinear Science (AREA)
- Mathematical Physics (AREA)
- Crystallography & Structural Chemistry (AREA)
- Polarising Elements (AREA)
- Laminated Bodies (AREA)
- Adhesive Tapes (AREA)
- Adhesives Or Adhesive Processes (AREA)
Abstract
本發明提供一種光學積層體,其具有薄型偏光件,並且該光學積層體之輸送性優異,且表面保護薄膜及分離件之剝離性優異。本發明之光學積層體具備:偏光板;黏著劑層,其設於該偏光板之一側;分離件,其係以可剝離之方式暫時黏著於該黏著劑層之與該偏光板相反之側;及表面保護薄膜,其係以可剝離之方式暫時黏著於該偏光板之與該黏著劑層相反之側;該偏光板之厚度為60µm以下;該表面保護薄膜之厚度為40µm以上,該表面保護薄膜之剝離力為0.10N/25mm~0.50N/25mm,該表面保護薄膜之彈性模數為2.00×109 Pa以上;該分離件之厚度為35µm~80µm,該分離件之剝離力小於0.28N/25mm。The present invention provides an optical laminate having a thin polarizing element, and the optical laminate has excellent transmission performance, and the surface protection film and the separation element have excellent peeling performance. The optical laminate of the present invention comprises: a polarizing plate; an adhesive layer disposed on one side of the polarizing plate; a separating piece temporarily adhered to the side of the adhesive layer opposite to the polarizing plate in a removable manner; and a surface protection film temporarily adhered to the side of the polarizing plate opposite to the adhesive layer in a removable manner; the thickness of the polarizing plate is less than 60µm; the thickness of the surface protection film is greater than 40µm, the peeling force of the surface protection film is 0.10N/25mm~0.50N/25mm, and the elastic modulus of the surface protection film is 2.00×10 9 Pa or above; the thickness of the separation piece is 35µm~80µm, and the peeling force of the separation piece is less than 0.28N/25mm.
Description
本發明係涉及光學積層體。The present invention relates to optical laminates.
在代表性影像顯示裝置的液晶顯示裝置中,依據其影像形成方式而於液晶單元的兩側配置有偏光件。偏光件代表上可藉由以碘等二色性物質將聚乙烯醇(PVA)系樹脂薄膜染色來製造(譬如專利文獻1及2)。近年來,影像顯示裝置的薄型化需求大增。所以,亦對偏光件要求進一步的薄型化。薄型偏光件(在實際應用上為包含該偏光件之偏光板)例如可以積層黏著劑層、表面保護薄膜及分離件而成之光學積層體來提供。但,這種光學積層體卻有輸送性不足、表面保護薄膜及分離件之剝離性不足等問題。 先前技術文獻 專利文獻In a liquid crystal display device, which is a representative image display device, polarizers are arranged on both sides of the liquid crystal unit according to its image formation method. Polarizers can be typically manufactured by dyeing a polyvinyl alcohol (PVA) resin film with a dichroic substance such as iodine (for example, patent documents 1 and 2). In recent years, the demand for thinner image display devices has increased greatly. Therefore, polarizers are also required to be further thinned. A thin polarizer (in actual application, a polarizing plate including the polarizer) can be provided, for example, by laminating an adhesive layer, a surface protection film, and a separator to form an optical laminate. However, this optical laminate has problems such as insufficient transportability and insufficient releasability of the surface protection film and the separator. Prior art literature Patent literature
專利文獻1:日本專利第5048120號公報 專利文獻2:日本專利特開2013-156391號公報Patent document 1: Japanese Patent No. 5048120 Patent document 2: Japanese Patent Publication No. 2013-156391
發明欲解決之課題 本發明係為了解決上述以往之課題而成者,其主要目的在於提供一種光學積層體,其係具有薄型偏光板、表面保護薄膜及分離件者,並且該光學積層體之輸送性優異,且表面保護薄膜及分離件之剝離性優異。 用以解決課題之手段Problem to be solved by the invention This invention is made to solve the above-mentioned previous problems. Its main purpose is to provide an optical laminate having a thin polarizing plate, a surface protection film and a separator. The optical laminate has excellent transport properties, and the surface protection film and the separator have excellent peeling properties. Means for solving the problem
本發明之光學積層體具備:偏光板;黏著劑層,其設於該偏光板之一側;分離件,其係以可剝離之方式暫時黏著於該黏著劑層之與該偏光板相反之側;及表面保護薄膜,其係以可剝離之方式暫時黏著於該偏光板之與該黏著劑層相反之側;該偏光板之厚度為60µm以下;該表面保護薄膜之厚度為40µm以上,該表面保護薄膜之剝離力為0.10N/25mm~0.50N/25mm,該表面保護薄膜之彈性模數為2.00×109 Pa以上;該分離件之厚度為35µm~80µm,該分離件之剝離力小於0.28N/25mm。 在一實施形態中,上述偏光件包含以含碘之聚乙烯醇系樹脂薄膜構成之偏光件。 在一實施形態中,上述偏光件之厚度為10μm以下。 在一實施形態中,上述偏光件之碘含量為10重量%~25重量%。 發明效果The optical laminate of the present invention comprises: a polarizing plate; an adhesive layer disposed on one side of the polarizing plate; a separating piece temporarily adhered to the side of the adhesive layer opposite to the polarizing plate in a removable manner; and a surface protection film temporarily adhered to the side of the polarizing plate opposite to the adhesive layer in a removable manner; the thickness of the polarizing plate is less than 60µm; the thickness of the surface protection film is greater than 40µm, the peeling force of the surface protection film is 0.10N/25mm~0.50N/25mm, and the elastic modulus of the surface protection film is 2.00×10 9 Pa or more; the thickness of the separation piece is 35µm~80µm, and the peeling force of the separation piece is less than 0.28N/25mm. In one embodiment, the polarizer comprises a polarizer formed of a polyvinyl alcohol-based resin film containing iodine. In one embodiment, the thickness of the polarizer is less than 10μm. In one embodiment, the iodine content of the polarizer is 10 wt%~25 wt%. Effect of the Invention
根據本發明,對於包含薄型偏光板、表面保護薄膜及分離件之光學積層體,藉由將該表面保護薄膜之厚度、剝離力及彈性模數、以及該分離件之厚度及剝離力最佳化,可實現輸送性優異且表面保護薄膜及分離件之剝離性優異的光學積層體。According to the present invention, for an optical laminate including a thin polarizing plate, a surface protection film and a separator, by optimizing the thickness, peeling force and elastic modulus of the surface protection film, and the thickness and peeling force of the separator, an optical laminate with excellent transportability and excellent peeling properties of the surface protection film and the separator can be achieved.
以下說明本發明之實施形態,惟本發明不受該等實施形態限定。The following describes the embodiments of the present invention, but the present invention is not limited to these embodiments.
A.光學積層體的整體構成
圖1係本發明之一實施形態的光學積層體的概略截面圖。圖式例之光學積層體100具有表面保護薄膜10、偏光板20、黏著劑層30與分離件40。偏光板20之厚度為60µm以下。並且,表面保護薄膜10之厚度為40µm以上,其剝離力為0.10N/25mm~0.50N/25mm,且其彈性模數為2.00×109
Pa以上。並且,分離件40之厚度為35µm~80µm,其剝離力小於0.28N/25mm。以下針對光學積層體之構成要素進行更詳細地說明。A. Overall Structure of Optical Laminated Body FIG1 is a schematic cross-sectional view of an optical laminated body in one embodiment of the present invention. The optical laminated
B.偏光板
偏光板20代表上具有偏光件22與配置於其單側或兩側的保護層。較佳為如圖式例,於偏光板20中,保護層21配置於偏光件22之單側。偏光板之厚度為60µm以下,宜為40µm以下,較宜為35µm以下。偏光板之厚度的下限可為例如20µm。B. Polarizing plate
The polarizing
B-1.偏光件
偏光件22代表上係以含有碘之聚乙烯醇(PVA)系樹脂薄膜構成。B-1. Polarizer
The
偏光件其厚度的上限在一實施形態中為10µm,在另一實施形態中為3µm。厚度的下限在一實施形態中為1µm。The upper limit of the thickness of the polarizer is 10 μm in one embodiment, and 3 μm in another embodiment. The lower limit of the thickness is 1 μm in one embodiment.
偏光件的碘含量可適當設定成可兼顧充分的偏光性能與最佳的單體透射率。碘含量宜為10重量%~25重量%,較宜為15重量%~25重量%。本發明實施形態所用偏光件即便具有如所述極高的碘含量,仍可實現以往難以實現之非常優異的耐熱性。更詳細而言,可在具有極高碘含量之偏光件中,顯著抑制在高溫環境下之光學特性之變化。本說明書中的「碘含量」意指偏光件(PVA系樹脂薄膜)中所含之所有碘的量。更具體而言,碘在偏光件中以碘離子(I- )、多碘離子(I3 - 、I5 - )等形態存在,而本說明書中的碘含量意指包含所有該等形態之碘的量。碘含量可利用譬如螢光X射線分析之檢量曲線法來算出。另,多碘離子在偏光件中係以形成有PVA-碘錯合物之狀態存在。藉由形成所述錯合物,可在可見光之波長範圍內展現吸收二色性。具體而言,PVA與三碘化物離子之錯合物(PVA・I3 - )在470nm附近具有吸光峰;PVA與五碘化物離子之錯合物(PVA・I5 - )在600nm附近具有吸光峰。結果,多碘離子可根據其形態在可見光之寬廣範圍內吸收光。另一方面,碘離子(I- )在230nm附近具有吸光峰,其與可見光之吸收無實質關聯。因此,以與PVA之錯合物狀態存在的多碘離子主要係與偏光件之吸收性能有關。The iodine content of the polarizer can be appropriately set to take into account both sufficient polarization performance and optimal single body transmittance. The iodine content is preferably 10% to 25% by weight, and more preferably 15% to 25% by weight. Even if the polarizer used in the embodiment of the present invention has an extremely high iodine content as described above, it can still achieve very excellent heat resistance that has been difficult to achieve in the past. In more detail, in a polarizer with an extremely high iodine content, the change of optical properties in a high temperature environment can be significantly suppressed. The "iodine content" in this specification refers to the amount of all iodine contained in the polarizer (PVA-based resin film). More specifically, iodine exists in the polarizer in the form of iodine ions ( I- ), polyiodine ions ( I3- , I5- ) , etc., and the iodine content in this specification refers to the amount of iodine including all such forms . The iodine content can be calculated using, for example, the calibration curve method of fluorescent X-ray analysis. In addition, polyiodine ions exist in the polarizer in the form of a PVA-iodine complex. By forming the complex, absorption dichroism can be exhibited in the wavelength range of visible light. Specifically, the complex of PVA and triiodide ion (PVA・I 3 - ) has an absorption peak near 470nm; the complex of PVA and pentaiodide ion (PVA・I 5 - ) has an absorption peak near 600nm. As a result, polyiodine ions can absorb light in a wide range of visible light depending on their form. On the other hand, iodine ion (I - ) has an absorption peak near 230nm, which has no substantial correlation with the absorption of visible light. Therefore, the polyiodine ions existing in the complex state with PVA are mainly related to the absorption performance of the polarizer.
偏光件之單體透射率(Ts)宜為30.0%~43.0%,較宜為35.0%~41.0%。偏光件的偏光度以99.9%以上為佳,99.95%以上較佳,99.98%以上更佳。透過將單體透射率設定得較低並將偏光度設得較高,可提高對比,可使黑顯示顯示得更黑,因此可實現一種具有優異畫質的影像顯示裝置。另,單體透射率係以附積分球之分光光度計測得之值。單體透射率係以JIS Z8701之2度視野(C光源)測定並進行視感度校正所得之Y值,舉例而言,可用附積分球之分光光度計(日本分光股份公司製,製品名:V7100)進行測定。The single body transmittance (Ts) of the polarizer is preferably 30.0%~43.0%, preferably 35.0%~41.0%. The polarization degree of the polarizer is preferably above 99.9%, preferably above 99.95%, and even more preferably above 99.98%. By setting the single body transmittance lower and the polarization degree higher, the contrast can be improved, and the black display can be made darker, so that an image display device with excellent image quality can be realized. In addition, the single body transmittance is a value measured by a spectrophotometer with an integrating sphere. The single body transmittance is measured with a 2 degree field of view (C light source) of JIS Z8701 and the Y value obtained by performing a visual sensitivity correction. For example, it can be measured using a spectrophotometer with an integrating sphere (manufactured by JASCO Corporation, product name: V7100).
B-2.PVA系樹脂薄膜 形成PVA系樹脂薄膜之PVA系樹脂可舉如聚乙烯醇、乙烯-乙烯醇共聚物。聚乙烯醇可藉由將聚乙酸乙烯酯皂化而得。乙烯-乙烯醇共聚物可藉由將乙烯-乙酸乙烯酯共聚物皂化而得。PVA系樹脂之皂化度通常為85莫耳%以上且低於100莫耳%,宜為95.0莫耳%~99.95莫耳%,較宜為99.0莫耳%~99.93莫耳%。皂化度可依循JIS K 6726-1994而求得。藉由使用所述皂化度的PVA系樹脂,可獲得耐久性優異的偏光件。皂化度太高時,會有膠化之虞。B-2. PVA resin film PVA resins used to form PVA resin films include polyvinyl alcohol and ethylene-vinyl alcohol copolymers. Polyvinyl alcohol can be obtained by saponifying polyvinyl acetate. Ethylene-vinyl alcohol copolymers can be obtained by saponifying ethylene-vinyl acetate copolymers. The saponification degree of PVA resins is usually 85 mol% or more and less than 100 mol%, preferably 95.0 mol% to 99.95 mol%, and more preferably 99.0 mol% to 99.93 mol%. The saponification degree can be obtained in accordance with JIS K 6726-1994. By using a PVA resin having the above saponification degree, a polarizer having excellent durability can be obtained. When the saponification degree is too high, there is a risk of gelling.
PVA系樹脂薄膜之厚度並無特別限制,可根據所期望之偏光件厚度設定。PVA系樹脂薄膜之厚度譬如為10μm~200μm。The thickness of the PVA resin film is not particularly limited and can be set according to the desired thickness of the polarizer. The thickness of the PVA resin film is, for example, 10 μm to 200 μm.
在一實施形態中,PVA系樹脂薄膜亦可為形成於基材上之PVA系樹脂層。基材與PVA系樹脂層之積層體可藉由譬如下述方法來獲得:將包含上述PVA系樹脂之塗佈液塗佈於基材之方法、將PVA系樹脂薄膜積層至基材之方法。基材可使用任意適當之樹脂基材,例如可使用熱塑性樹脂基材。In one embodiment, the PVA-based resin film may be a PVA-based resin layer formed on a substrate. The laminate of the substrate and the PVA-based resin layer may be obtained by, for example, the following methods: a method of applying a coating liquid containing the above-mentioned PVA-based resin to the substrate, a method of laminating the PVA-based resin film on the substrate. The substrate may be any appropriate resin substrate, for example, a thermoplastic resin substrate.
B-3.保護層 保護層可使用任意適當的樹脂薄膜。樹脂薄膜之形成材料可舉如(甲基)丙烯酸系樹脂、二醋酸纖維素、三醋酸纖維素等纖維素系樹脂、降莰烯系樹脂等環烯烴系樹脂、聚丙烯等烯烴系樹脂、聚對苯二甲酸乙二酯系樹脂等酯系樹脂、聚醯胺系樹脂、聚碳酸酯系樹脂及該等之共聚物樹脂。另,「(甲基)丙烯酸系樹脂」意指丙烯酸系樹脂及/或甲基丙烯酸系樹脂。B-3. Protective layer Any appropriate resin film can be used for the protective layer. The material forming the resin film can include (meth) acrylic resin, cellulose resins such as cellulose diacetate and cellulose triacetate, cycloolefin resins such as norbornene resins, olefin resins such as polypropylene, ester resins such as polyethylene terephthalate resins, polyamide resins, polycarbonate resins, and copolymer resins thereof. In addition, "(meth) acrylic resin" means acrylic resin and/or methacrylic resin.
在一實施形態中,上述(甲基)丙烯酸系樹脂係使用具有戊二醯亞胺結構之(甲基)丙烯酸系樹脂。具有戊二醯亞胺結構之(甲基)丙烯酸系樹脂(以下亦稱戊二醯亞胺樹脂)譬如係記載於下列文獻中:日本專利特開2006-309033號公報、日本專利特開2006-317560號公報、日本專利特開2006-328329號公報、日本專利特開2006-328334號公報、日本專利特開2006-337491號公報、日本專利特開2006-337492號公報、日本專利特開2006-337493號公報、日本專利特開2006-337569號公報、日本專利特開2007-009182號公報、日本專利特開2009-161744號公報及日本專利特開2010-284840號公報。本說明書中援引該等記載作為參考。In one embodiment, the (meth)acrylic resin is a (meth)acrylic resin having a glutarimide structure. The (meth)acrylic resin having a glutarimide structure (hereinafter also referred to as a glutarimide resin) is described in, for example, Japanese Patent Laid-Open No. 2006-309033, Japanese Patent Laid-Open No. 2006-317560, Japanese Patent Laid-Open No. 2006-328329, Japanese Patent Laid-Open No. 2006-328334, Japanese Patent Laid-Open No. 2006-309033, Japanese Patent Laid-Open No. 2006-317560, Japanese Patent Laid-Open No. 2006-328329, Japanese Patent Laid-Open No. 2006-328334, Japanese Patent Laid-Open No. 2006-309033, Japanese Patent Laid-Open No. 2006-317560, Japanese Patent Laid-Open No. 2006-328329, Japanese Patent Laid-Open No. 2006-328334, Japanese Patent Laid-Open No. 2006-309033, Japanese Patent Laid-Open No. 2006-317560, Japanese Patent Laid-Open No. 2006-328334 ... 6-337491, Japanese Patent Publication No. 2006-337492, Japanese Patent Publication No. 2006-337493, Japanese Patent Publication No. 2006-337569, Japanese Patent Publication No. 2007-009182, Japanese Patent Publication No. 2009-161744 and Japanese Patent Publication No. 2010-284840. These descriptions are incorporated herein by reference.
使用基材與PVA系樹脂層之積層體來製造偏光件時,亦可無須剝離基材而直接作為保護層使用。又,亦可剝離基材後於偏光件貼合保護層。When a laminate of a substrate and a PVA-based resin layer is used to manufacture a polarizer, the substrate can be used directly as a protective layer without peeling off the substrate. Alternatively, the protective layer can be attached to the polarizer after peeling off the substrate.
保護層的厚度宜為5mm以下,較宜為1mm以下,更宜為1µm~500µm,最宜為5µm~150µm。另外,在施有表面處理時,保護層之厚度係包含表面處理層之厚度的厚度。The thickness of the protective layer is preferably less than 5 mm, more preferably less than 1 mm, more preferably 1µm to 500µm, and most preferably 5µm to 150µm. In addition, when surface treatment is applied, the thickness of the protective layer includes the thickness of the surface treatment layer.
保護層係透過任意適當的接著層(接著劑層、黏著劑層)貼合於偏光件。The protective layer is attached to the polarizer through any appropriate bonding layer (bonding agent layer, adhesive layer).
C.表面保護薄膜
如圖式例所示,表面保護薄膜10係以可剝離之方式暫時黏著於偏光板20之與黏著劑層30相反之側。更詳細而言,表面保護薄膜10包含基材薄膜與黏著劑層,且透過該黏著劑層貼合表面保護薄膜10與偏光板20。C. Surface protection film
As shown in the example of the figure, the
C-1.基材薄膜 表面保護薄膜之基材薄膜可以任意適當的樹脂薄膜構成。樹脂薄膜之形成材料可舉聚對苯二甲酸乙二酯系樹脂等酯系樹脂、降莰烯系樹脂等環烯烴系樹脂、聚丙烯等烯烴系樹脂、聚醯胺系樹脂、聚碳酸酯系樹脂、其等之共聚物樹脂等。較理想的是酯系樹脂(尤為聚對苯二甲酸乙二酯系樹脂)。只要為所述材料,便具有彈性模數夠高且即便於輸送及/或貼合時加諸張力亦不易發生變形之優點。C-1. Base film The base film of the surface protection film can be made of any appropriate resin film. The forming material of the resin film can include ester resins such as polyethylene terephthalate resins, cycloolefin resins such as norbornene resins, olefin resins such as polypropylene, polyamide resins, polycarbonate resins, and copolymer resins thereof. Ester resins (especially polyethylene terephthalate resins) are more desirable. As long as it is the above-mentioned material, it has the advantages of having a high elastic modulus and not easily deforming even when tension is applied during transportation and/or bonding.
基材薄膜的厚度宜為38µm以上,較宜為48µm以上。基材薄膜之厚度的上限可為例如128µm。只要為所述厚度,便具有即便於輸送及/或貼合時加諸張力亦不易發生變形之優點。The thickness of the substrate film is preferably 38 μm or more, more preferably 48 μm or more. The upper limit of the thickness of the substrate film may be, for example, 128 μm. As long as the thickness is the above, it has the advantage that it is not easy to deform even when tension is applied during transportation and/or lamination.
C-2.黏著劑層 形成上述表面保護薄膜中之黏著劑層的黏著劑可採用任意適當之黏著劑。黏著劑的基底樹脂可舉例如丙烯酸系樹脂、苯乙烯系樹脂、聚矽氧系樹脂。由耐藥品性、為防止浸漬時處理液滲入之密著性、對被黏著體之自由度等觀點來看,宜為丙烯酸系樹脂。可含於黏著劑中之交聯劑可舉例如異氰酸酯化合物、環氧化合物、 化合物。黏著劑亦可包含有例如矽烷耦合劑。黏著劑之摻混處方可按目的適當設定。C-2. Adhesive layer Any appropriate adhesive may be used as the adhesive forming the adhesive layer in the surface protection film. Examples of the base resin of the adhesive include acrylic resins, styrene resins, and silicone resins. From the viewpoints of chemical resistance, adhesion to prevent the treatment liquid from penetrating during immersion, and the degree of freedom for the adherend, acrylic resins are preferred. Examples of crosslinking agents that may be contained in the adhesive include isocyanate compounds, epoxy compounds, The adhesive may also contain, for example, a silane coupling agent. The mixing formula of the adhesive may be appropriately set according to the purpose.
上述黏著劑層之厚度宜為2µm以上,較宜為5µm以上。厚度的上限例如為40µm。The thickness of the adhesive layer is preferably 2µm or more, more preferably 5µm or more. The upper limit of the thickness is, for example, 40µm.
C-3.表面保護薄膜之特性 表面保護薄膜之厚度為40µm以上,宜為50µm以上。表面保護薄膜之厚度的上限可為例如130µm。此外,表面保護薄膜之厚度係指基材薄膜與黏著劑層之厚度的合計。藉由表面保護薄膜的厚度為所述範圍,可獲得輸送性優異的光學積層體。表面保護薄膜的厚度若較40µm更薄,則輸送性會變不足。C-3. Characteristics of surface protection film The thickness of the surface protection film is 40µm or more, preferably 50µm or more. The upper limit of the thickness of the surface protection film may be, for example, 130µm. In addition, the thickness of the surface protection film refers to the total thickness of the base film and the adhesive layer. When the thickness of the surface protection film is within the above range, an optical laminate with excellent transport properties can be obtained. If the thickness of the surface protection film is thinner than 40µm, the transport properties will become insufficient.
表面保護薄膜之剝離力為0.10N/25mm~0.50N/25mm,且宜為0.10N/25mm~0.35N/25mm。藉由表面保護薄膜之剝離力為所述範圍,可獲得表面保護薄膜及分離件之剝離性優異的光學積層體。表面保護薄膜之剝離力若小於0.10N/25mm,則在分離件剝離時會發生表面保護薄膜浮凸。進而,若大於0.50N/25mm,則在表面保護薄膜剝離時會發生剝層。The peeling force of the surface protection film is 0.10N/25mm~0.50N/25mm, and preferably 0.10N/25mm~0.35N/25mm. When the peeling force of the surface protection film is within the above range, an optical laminate with excellent peeling properties of the surface protection film and the separation piece can be obtained. If the peeling force of the surface protection film is less than 0.10N/25mm, the surface protection film will be embossed when the separation piece is peeled off. Furthermore, if it is greater than 0.50N/25mm, delamination will occur when the surface protection film is peeled off.
表面保護薄膜之彈性模數為2.00×109 Pa以上,且宜為2.50×109 Pa以上。表面保護薄膜之彈性模數的上限可為8.00×109 Pa。藉由表面保護薄膜的彈性模數為所述範圍,可獲得輸送性優異的光學積層體。表面保護薄膜之彈性模數若小於2.00×109 Pa,則有於輸送中發生薄膜的皺褶及彎折的情形。The elastic modulus of the surface protection film is 2.00×10 9 Pa or more, and preferably 2.50×10 9 Pa or more. The upper limit of the elastic modulus of the surface protection film may be 8.00×10 9 Pa. When the elastic modulus of the surface protection film is within the above range, an optical laminate having excellent transportability can be obtained. If the elastic modulus of the surface protection film is less than 2.00×10 9 Pa, wrinkles and bends of the film may occur during transport.
D.黏著劑層
黏著劑層30代表上可以丙烯酸系黏著劑構成。如圖式例所示,黏著劑層30形成於偏光板20之一面,係為了貼附液晶面板與偏光板20而設置。D. Adhesive layer
The
黏著劑層的厚度宜為100µm以下,較宜為50µm以下,更宜為30µm以下。厚度的下限可為例如1µm。The thickness of the adhesive layer is preferably 100 μm or less, more preferably 50 μm or less, and even more preferably 30 μm or less. The lower limit of the thickness may be, for example, 1 μm.
E.分離件
如圖式例所示,分離件40係以可剝離之方式暫時黏著於黏著劑層30之與偏光板20相反之側。分離件可保護黏著劑層直至實際使用前,並可形成成偏光板之捲料。E. Separation piece
As shown in the figure, the
分離件的形成材料可舉例如聚對苯二甲酸乙二酯系樹脂等酯系樹脂、降莰烯系樹脂等環烯烴系樹脂、聚丙烯等烯烴樹脂、聚醯胺系樹脂、聚碳酸酯系樹脂及其等之共聚物樹脂。較理想的是酯系樹脂(尤為聚對苯二甲酸乙二酯系樹脂)。The material for forming the separation element includes, for example, ester resins such as polyethylene terephthalate resins, cycloolefin resins such as norbornene resins, olefin resins such as polypropylene, polyamide resins, polycarbonate resins and copolymer resins thereof. Preferably, ester resins (especially polyethylene terephthalate resins) are used.
分離件之厚度為35µm~80µm,且宜為40µm~60µm。藉由分離件之厚度為所述範圍,可獲得輸送性優異且分離件之剝離性優異的光學積層體。分離件的厚度若較35µm更薄,則輸送性會變不足。進而,若分離件之厚度較80µm更厚,則在分離件剝離時會發生拾取不良。The thickness of the separation piece is 35µm to 80µm, and preferably 40µm to 60µm. By making the thickness of the separation piece within the above range, an optical laminate having excellent transportability and excellent peeling property of the separation piece can be obtained. If the thickness of the separation piece is thinner than 35µm, the transportability becomes insufficient. Furthermore, if the thickness of the separation piece is thicker than 80µm, poor picking occurs when the separation piece is peeled off.
分離件之剝離力小於0.28N/25mm,且宜小於0.10N/25mm。藉由分離件之剝離力為所述範圍,可獲得分離件之剝離性優異的光學積層體。分離件之剝離力若為0.28N/25mm以上,則在分離件剝離時會發生拾取不良。The peeling force of the separation piece is less than 0.28N/25mm, and preferably less than 0.10N/25mm. When the peeling force of the separation piece is within the above range, an optical laminate having excellent peeling property of the separation piece can be obtained. If the peeling force of the separation piece is greater than 0.28N/25mm, poor picking will occur when the separation piece is peeled.
F.光學積層體之製造方法 F-1.偏光件 本發明實施形態之偏光件之製造方法包含將PVA系樹脂薄膜至少進行延伸及染色。代表上,該製造方法包含準備PVA系樹脂薄膜之步驟、延伸步驟、染色步驟、交聯步驟、洗淨步驟及乾燥步驟。又,亦可因應需要於延伸步驟前具有膨潤步驟。供有PVA系樹脂薄膜的各步驟可以任意適當的順序及時序進行。因此,各步驟可按上述順序進行,亦可以不同於上述之順序進行。亦可因應需求將1個步驟進行多次。此外,上述以外之步驟(譬如不溶解步驟)可以任意適當的時序進行。另,當PVA系樹脂薄膜為形成於基材上之PVA系樹脂層時,可將基材與PVA系樹脂層之積層體供於上述步驟。F. Method for manufacturing optical laminates F-1. Polarizer The method for manufacturing a polarizer in an embodiment of the present invention includes at least stretching and dyeing a PVA-based resin film. Typically, the manufacturing method includes a step of preparing a PVA-based resin film, a stretching step, a dyeing step, a cross-linking step, a washing step, and a drying step. In addition, a swelling step may be provided before the stretching step as required. The steps of providing the PVA-based resin film may be performed in any appropriate order and timing. Therefore, each step may be performed in the above order or in a different order from the above order. One step may also be performed multiple times as required. In addition, steps other than the above (such as the insolubilization step) can be performed at any appropriate time sequence. In addition, when the PVA-based resin film is a PVA-based resin layer formed on a substrate, the laminate of the substrate and the PVA-based resin layer can be provided to the above steps.
以下說明各步驟,惟如上述,各步驟可以任意適當的順序進行,不受記載順序所限制。The following describes each step, but as mentioned above, each step can be performed in any appropriate order and is not limited to the order in which it is described.
(延伸步驟) 在延伸步驟中,PVA系樹脂薄膜代表上係被單軸延伸至3倍~7倍。延伸方向可為薄膜之長邊方向(MD方向),亦可為薄膜之寬度方向(TD方向)。延伸方法可為乾式延伸,亦可為濕式延伸,或可將該等予以組合。又,亦可在進行交聯步驟、膨潤步驟、染色步驟等時將PVA系樹脂薄膜予以延伸。另,延伸方向可對應所得偏光件的吸收軸方向。(Stretching step) In the stretching step, the PVA resin film is typically uniaxially stretched to 3 to 7 times. The stretching direction can be the long side direction (MD direction) of the film or the width direction (TD direction) of the film. The stretching method can be dry stretching or wet stretching, or a combination of these. In addition, the PVA resin film can be stretched during the crosslinking step, swelling step, dyeing step, etc. In addition, the stretching direction can correspond to the absorption axis direction of the obtained polarizer.
(膨潤步驟) 膨潤步驟通常係在染色步驟前進行。膨潤步驟譬如可藉由將PVA系樹脂薄膜浸漬於膨潤浴中來進行。膨潤浴通常可用蒸餾水、純水等水。膨潤浴亦可含有水以外之任意適當的其他成分。其他成分可舉醇類等溶劑、界面活性劑等添加劑、碘化物等。碘化物可舉例如碘化鉀、碘化鋰、碘化鈉、碘化鋅、碘化鋁、碘化鉛、碘化銅、碘化鋇、碘化鈣、碘化錫、碘化鈦。宜使用碘化鉀。膨潤浴之溫度譬如為20℃~45℃。又,浸漬時間譬如為10秒~300秒。(Swelling step) The swelling step is usually performed before the dyeing step. The swelling step can be performed, for example, by immersing the PVA resin film in a swelling bath. The swelling bath can usually be water such as distilled water or pure water. The swelling bath can also contain any other appropriate components other than water. Other components can include solvents such as alcohols, additives such as surfactants, and iodides. Iodides can include potassium iodide, lithium iodide, sodium iodide, zinc iodide, aluminum iodide, lead iodide, copper iodide, barium iodide, calcium iodide, tin iodide, and titanium iodide. Potassium iodide is preferably used. The temperature of the swelling bath is, for example, 20°C to 45°C. In addition, the immersion time is, for example, 10 seconds to 300 seconds.
(染色步驟) 染色步驟係以二色性物質將PVA系樹脂薄膜進行染色之步驟。宜藉由使其吸附二色性物質來進行。該吸附方法可舉如:使PVA系樹脂薄膜浸漬於含二色性物質之染色液中的方法、將該染色液塗敷於PVA系樹脂薄膜上的方法、及將該染色液噴霧至PVA系樹脂薄膜的方法。理想為使PVA系樹脂薄膜浸漬於染色液中的方法。因為可良好吸附二色性物質。(Dyeing step) The dyeing step is a step of dyeing the PVA resin film with a dichroic substance. It is preferably performed by making it adsorb the dichroic substance. The adsorption method includes: a method of immersing the PVA resin film in a dyeing liquid containing the dichroic substance, a method of applying the dyeing liquid on the PVA resin film, and a method of spraying the dyeing liquid on the PVA resin film. The method of immersing the PVA resin film in the dyeing liquid is ideal because the dichroic substance can be well adsorbed.
上述二色性物質可舉如碘、二色性染料。且以碘為宜。採用碘作為二色性物質時,染色液宜使用碘水溶液。碘水溶液之碘含量相對於水100重量份宜為0.04重量份~5.0重量份。為了提高碘對水的溶解度,宜於碘水溶液中摻混碘化物。碘化物宜使用碘化鉀。碘化物含量相對於水100重量份宜為0.3重量份~15重量份。The above-mentioned dichroic substance can be iodine and dichroic dyes. Iodine is preferred. When iodine is used as the dichroic substance, an iodine aqueous solution is preferably used as the dyeing liquid. The iodine content of the iodine aqueous solution is preferably 0.04 to 5.0 parts by weight relative to 100 parts by weight of water. In order to increase the solubility of iodine in water, iodide is preferably mixed in the iodine aqueous solution. Potassium iodide is preferably used as the iodide. The iodide content is preferably 0.3 to 15 parts by weight relative to 100 parts by weight of water.
染色液於染色時之液溫可設定成任意且適當之值,舉例如20℃~50℃。使PVA系樹脂薄膜浸漬於染色液時,浸漬時間譬如為5秒~5分鐘。The temperature of the dyeing solution during dyeing can be set to any appropriate value, for example, 20° C. to 50° C. When the PVA resin film is immersed in the dyeing solution, the immersion time is, for example, 5 seconds to 5 minutes.
(交聯步驟) 在交聯步驟中,通常係使用硼化合物作為交聯劑。硼化合物可舉例如硼酸、硼砂。且以硼酸為宜。在交聯步驟中,硼化合物通常係以水溶液之形態作使用。(Crosslinking step) In the crosslinking step, a boron compound is usually used as a crosslinking agent. Examples of the boron compound include boric acid and borax. Boric acid is preferred. In the crosslinking step, the boron compound is usually used in the form of an aqueous solution.
使用硼酸水溶液時,硼酸水溶液之硼酸濃度譬如為1重量%~15重量%,宜為1重量%~10重量%。更可使硼酸水溶液中含有碘化鉀等碘化物、硫酸鋅、氯化鋅等鋅化合物。When a boric acid aqueous solution is used, the boric acid concentration of the boric acid aqueous solution is, for example, 1% to 15% by weight, preferably 1% to 10% by weight. The boric acid aqueous solution may further contain iodides such as potassium iodide, zinc compounds such as zinc sulfate and zinc chloride.
交聯步驟可以任意適當的方法進行。譬如可舉:將PVA系樹脂薄膜浸漬於含硼化合物之水溶液中的方法、將含硼化合物之水溶液塗佈至PVA系樹脂薄膜的方法、或是將含硼化合物之水溶液噴霧至PVA系樹脂薄膜的方法。以浸漬於含硼化合物之水溶液中為宜。The crosslinking step can be performed by any appropriate method. For example, the method of immersing the PVA resin film in an aqueous solution of a boron compound, the method of applying the aqueous solution of a boron compound to the PVA resin film, or the method of spraying the aqueous solution of a boron compound to the PVA resin film. Preferably, the method of immersing the film in an aqueous solution of a boron compound is performed.
用於交聯之溶液的溫度譬如為25℃以上,宜為30℃~85℃,較宜為40℃~70℃。浸漬時間譬如為5秒~800秒,宜為8秒~500秒。The temperature of the solution used for crosslinking is, for example, above 25° C., preferably 30° C. to 85° C., more preferably 40° C. to 70° C. The immersion time is, for example, 5 seconds to 800 seconds, preferably 8 seconds to 500 seconds.
(洗淨步驟) 洗淨步驟代表上係在交聯步驟後進行。洗淨步驟代表上係使PVA系樹脂薄膜浸漬於洗淨液中來進行。洗淨液之代表例可舉純水。亦可於純水中添加碘化鉀。(Washing step) The washing step is typically performed after the crosslinking step. The washing step is typically performed by immersing the PVA-based resin film in a washing solution. A typical example of the washing solution is pure water. Potassium iodide may also be added to pure water.
洗淨液溫度譬如為5℃~50℃。浸漬時間譬如為1秒~300秒。The cleaning liquid temperature is, for example, 5°C to 50°C. The immersion time is, for example, 1 second to 300 seconds.
(乾燥步驟) 乾燥步驟可以任意適當的方法進行。乾燥方法可舉如自然乾燥、送風乾燥、減壓乾燥、加熱乾燥。且宜使用加熱乾燥。由乾燥時間縮短的觀點來看,進行加熱乾燥時,加熱溫度譬如為30℃~100℃。在另一實施形態中,宜為50℃以下,較宜為45℃以下,更宜為40℃以下。加熱溫度之下限並無特別限定,而為可在加熱乾燥裝置設定之下限溫度。例如為30℃。藉由將乾燥步驟之加熱溫度設成所述範圍,可將偏光件的游離硼酸含量調整至預定範圍內。又,乾燥時間譬如為20秒~10分鐘。在一實施形態中,係以2階段以上進行加熱乾燥。此時,宜至少有任一階段的加熱溫度為上述範圍內之溫度。要進行加熱乾燥時,將加熱溫度設於上述範圍內,可獲得具有非常優異耐熱性之偏光件。(Drying step) The drying step can be performed by any appropriate method. Examples of drying methods include natural drying, air drying, reduced pressure drying, and heating drying. Heating drying is preferably used. From the perspective of shortening the drying time, when performing heating drying, the heating temperature is, for example, 30°C to 100°C. In another embodiment, it is preferably below 50°C, more preferably below 45°C, and more preferably below 40°C. The lower limit of the heating temperature is not particularly limited, but is a lower limit temperature that can be set in the heating drying device. For example, it is 30°C. By setting the heating temperature of the drying step to the above range, the free boric acid content of the polarizer can be adjusted to within a predetermined range. In addition, the drying time is, for example, 20 seconds to 10 minutes. In one embodiment, the heat drying is performed in two or more stages. At this time, it is preferred that the heating temperature of at least one stage is within the above range. When the heat drying is performed, the heating temperature is set within the above range, and a polarizer with excellent heat resistance can be obtained.
F-2.偏光板 於上述F-1中所得偏光件表面(與樹脂基材相反之側的面)貼合作為保護層之樹脂薄膜。接著,藉由剝離該樹脂基材,可獲得具有保護層/偏光件之構成的偏光板。亦可視需求於剝離面貼合成為另一保護層之樹脂薄膜。F-2. Polarizing plate A resin film as a protective layer is bonded to the surface of the polarizing element obtained in F-1 (the surface opposite to the resin substrate). Then, by peeling off the resin substrate, a polarizing plate having a protective layer/polarizing element structure can be obtained. Alternatively, a resin film as another protective layer can be bonded to the peeled surface as required.
F-3.光學積層體
於上述F-2中所得偏光板的偏光件側形成黏著劑層,並於該黏著劑層表面以可剝離之方式暫時黏著分離件。並於該偏光板之與黏著劑層相反之側的面以可剝離之方式暫時黏著表面保護薄膜,藉此可獲得光學積層體100。
實施例F-3. Optical laminate
An adhesive layer is formed on the polarizing element side of the polarizing plate obtained in F-2 above, and a separation element is temporarily adhered to the surface of the adhesive layer in a releasable manner. A surface protection film is temporarily adhered to the surface of the polarizing plate opposite to the adhesive layer in a releasable manner, thereby obtaining an
以下,以實施例來具體說明本發明,惟本發明不受該等實施例限定。又,各特性之測定方法如以下所述。The present invention is specifically described below with reference to the embodiments, but the present invention is not limited to the embodiments. The measuring methods of each characteristic are as follows.
(1)輸送性 在一邊使偏光板表面接觸導輥一邊輸送的步驟中,以肉眼確認是否發生偏光板之彎折、傷痕等。輸送速度設為5m/分鐘~30m/分鐘。 ○:可無問題地輸送。 △:雖於輸送中捲入輥中,但無產生彎折、傷痕等。 ×:於輸送中捲入輥中,產生彎折、傷痕等。 (2)表面保護薄膜的剝離評估 於表面保護薄膜之角貼合起點膠帶(NICHIBAN公司製,CELLOTAPE(註冊商標)CT-24),以肉眼確認剝離表面保護薄膜時之剝離狀態。 ○:可無問題地剝離表面保護薄膜。 △:鮮少有表面保護薄膜未追隨起點膠帶之情形。成功率為80%~100%。 ×:表面保護薄膜未追隨起點膠帶。成功率為80%以下。即便可剝離表面保護薄膜,也會發生分離件之浮凸、偏光板之剝層。 (3)分離件之剝離評估 於分離件之角貼合起點膠帶(NICHIBAN公司製,CELLOTAPE(註冊商標)CT-24),以肉眼確認剝離分離件時之剝離狀態。 ○:可無問題地剝離分離件。 △:鮮少有分離薄膜未追隨起點膠帶之情形。成功率為80%~100%。 ×:分離薄膜未追隨起點膠帶。成功率為80%以下。或者在表面保護薄膜/偏光薄膜之間剝離。 (4)表面保護薄膜之剝離力 將上述光學積層體裁切成25mm×150mm之大小並剝離分離件後,以黏著劑層面與玻璃相接之方式作貼合。使用黏著皮膜剝離解析裝置(協和界面科學股份公司製,型式:VPA-2)測定於90°方向在300mm/分鐘之速度下剝離表面保護薄膜時的應力(N/25mm)。測定溫度設為25℃。 (5)分離件之剝離力 將上述光學積層體裁切成25mm×150mm之大小,並於附雙面膠帶之玻璃(日東電工公司製,No.500)上以表面保護薄膜面與雙面膠帶相接之方式作貼合。使用黏著皮膜剝離解析裝置(協和界面科學股份公司製,型式:VPA-2)測定於90°方向在300mm/分鐘之速度下剝離分離件時的應力(N/25mm)。測定溫度設為25℃。(1) Transportability While transporting the polarizing plate while contacting the surface of the polarizing plate with the guide roller, check with the naked eye whether the polarizing plate is bent or scratched. The transport speed is set to 5m/min to 30m/min. ○: Transported without any problems. △: Although it is rolled into the roller during transport, no bends or scratches are generated. ×: It is rolled into the roller during transport and bends or scratches are generated. (2) Evaluation of peeling of surface protective film A starting tape (manufactured by NICHIBAN, CELLOTAPE (registered trademark) CT-24) is attached to the corner of the surface protective film, and the peeling state of the surface protective film is checked with the naked eye. ○: The surface protection film can be peeled off without any problem. △: The surface protection film rarely fails to follow the starting tape. The success rate is 80% to 100%. ×: The surface protection film fails to follow the starting tape. The success rate is less than 80%. Even if the surface protection film can be peeled off, embossing of the separation piece and delamination of the polarizing plate may occur. (3) Evaluation of separation piece peeling A starting tape (manufactured by NICHIBAN, CELLOTAPE (registered trademark) CT-24) is attached to the corner of the separation piece, and the peeling state of the separation piece is confirmed by naked eyes. ○: The separation piece can be peeled off without any problem. △: There are few cases where the separation film does not follow the starting tape. The success rate is 80%~100%. ×: The separation film does not follow the starting tape. The success rate is less than 80%. Or it is peeled between the surface protection film/polarizing film. (4) Peeling force of surface protection film The above optical laminate was cut into a size of 25mm×150mm and the separation piece was peeled off, and then bonded in such a way that the adhesive layer was in contact with the glass. The stress (N/25mm) when the surface protection film was peeled off at a speed of 300mm/min in the 90° direction was measured using an adhesive film peeling analyzer (manufactured by Kyowa Interface Science Co., Ltd., model: VPA-2). The measuring temperature was set to 25℃. (5) Peeling force of separated parts The optical laminate was cut into a size of 25 mm × 150 mm and attached to glass with double-sided tape (Nitto Denko Co., Ltd., No. 500) with the surface protection film surface in contact with the double-sided tape. The stress (N/25 mm) when the separated parts were peeled at a speed of 300 mm/min in the 90° direction was measured using an adhesive film peeling analysis device (Kyowa Interface Science Co., Ltd., model: VPA-2). The measuring temperature was set to 25°C.
[實施例1] 熱塑性樹脂基材係使用吸水率0.75%、Tg75℃之非晶質間苯二甲酸共聚聚對苯二甲酸乙二酯(IPA共聚PET)薄膜(厚度:100μm)。於基材單面施以電暈處理,並於該電暈處理面上於25℃下塗佈以9:1之比含有聚乙烯醇(聚合度4200,皂化度99.2莫耳%)及乙醯乙醯基改質PVA(聚合度1200,乙醯乙醯基改質度4.6%,皂化度99.0莫耳%以上,日本合成化學工業公司製,商品名「GOHSEFIMER Z200」)之水溶液後使其乾燥,而形成厚度11μm之PVA系樹脂層,製出積層體。 用拉幅延伸機將所得之積層體在140℃下往與積層體之長邊方向正交之方向進行4.5倍空中延伸(延伸處理)。 接著,使積層體浸漬於液溫25℃之染色浴(碘濃度1.4重量%及碘化鉀濃度9.8重量%之水溶液)中12秒鐘,進行染色(染色處理)。 接下來使積層體浸漬於液溫25℃之洗淨浴(純水)中6秒鐘(第1洗淨處理)。 再來使之浸漬於液溫60℃之交聯浴(硼濃度1重量%及碘化鉀濃度1重量%之水溶液)中16秒鐘(交聯處理)。 接著使積層體浸漬於液溫25℃之洗淨浴(碘化鉀濃度1重量%之水溶液)中3秒鐘(第2洗淨處理)。 然後以40℃之烘箱使積層體乾燥8秒鐘(第1乾燥處理)。 最後,以40℃之烘箱使積層體乾燥13秒鐘(第2乾燥處理),而獲得具有厚度1.2μm之PVA系樹脂層(偏光件)的積層體(偏光板)。所得偏光件的碘含量為18.6重量%,單體透射率為39.9%。 於上述所得偏光板之偏光件側表面形成黏著劑層,並於該黏著劑層表面以可剝離之方式暫時黏著分離件。並於偏光板之與黏著劑層相反之側的面以可剝離之方式暫時黏著表面保護薄膜,而獲得光學積層體。將所得光學積層體供於上述(1)~(3)之評估。將結果列於表1。[Example 1] The thermoplastic resin substrate is an amorphous isophthalic acid copolymer polyethylene terephthalate (IPA copolymer PET) film (thickness: 100μm) with a water absorption rate of 0.75% and a Tg of 75℃. A corona treatment is applied to one side of the substrate, and an aqueous solution containing polyvinyl alcohol (polymerization degree 4200, saponification degree 99.2 mol%) and acetoacetyl modified PVA (polymerization degree 1200, acetoacetyl modification degree 4.6%, saponification degree 99.0 mol% or more, manufactured by Nippon Synthetic Chemical Industry Co., Ltd., trade name "GOHSEFIMER Z200") in a ratio of 9:1 is applied to the corona treated surface at 25℃ and then dried to form a PVA resin layer with a thickness of 11μm to produce a laminate. The obtained laminate was stretched in the air 4.5 times at 140°C in a direction perpendicular to the long side direction of the laminate using a tenter stretching machine (stretching treatment). Then, the laminate was immersed in a dyeing bath (an aqueous solution with an iodine concentration of 1.4% by weight and a potassium iodide concentration of 9.8% by weight) at a liquid temperature of 25°C for 12 seconds to be dyed (dyeing treatment). Next, the laminate was immersed in a cleaning bath (pure water) at a liquid temperature of 25°C for 6 seconds (first cleaning treatment). Then, it was immersed in a crosslinking bath (an aqueous solution with a boron concentration of 1% by weight and a potassium iodide concentration of 1% by weight) at a liquid temperature of 60°C for 16 seconds (crosslinking treatment). The laminate was then immersed in a cleaning bath (aqueous solution of potassium iodide with a concentration of 1% by weight) at a liquid temperature of 25°C for 3 seconds (second cleaning treatment). Then the laminate was dried in an oven at 40°C for 8 seconds (first drying treatment). Finally, the laminate was dried in an oven at 40°C for 13 seconds (second drying treatment), and a laminate (polarizing plate) having a PVA-based resin layer (polarizer) with a thickness of 1.2μm was obtained. The iodine content of the obtained polarizer was 18.6% by weight, and the single body transmittance was 39.9%. An adhesive layer is formed on the polarizer side surface of the polarizing plate obtained above, and a separation piece is temporarily adhered to the adhesive layer surface in a removable manner. A surface protection film is temporarily adhered to the side of the polarizing plate opposite to the adhesive layer in a removable manner to obtain an optical laminate. The obtained optical laminate is subjected to the evaluations of (1) to (3) above. The results are listed in Table 1.
[實施例2~12及比較例1~10] 如表1所示,變更表面保護薄膜之厚度、剝離力及彈性模數、以及分離件之厚度及剝離力,除此之外依與實施例1相同方式而獲得光學積層體。將所得光學積層體供於與實施例1相同之評估。將結果列於表1。 [表1] [Examples 2 to 12 and Comparative Examples 1 to 10] As shown in Table 1, the thickness, peeling force and elastic modulus of the surface protection film, and the thickness and peeling force of the separation member were changed, and an optical laminate was obtained in the same manner as in Example 1. The obtained optical laminate was subjected to the same evaluation as in Example 1. The results are listed in Table 1. [Table 1]
由表1明顯可知,本發明之實施例(尤其是實施例1)的光學積層體,其輸送性優異,且表面保護薄膜的剝離性及分離件之剝離性優異。 由比較例1可知,表面保護薄膜之厚度若小於40µm,輸送性就會不夠充分。由比較例2及比較例5可知,表面保護薄膜之剝離力若大於0.50N/25mm,則在表面保護薄膜剝離時會發生剝層,而由比較例3及比較例4可知,表面保護薄膜之剝離力若小於0.10N/25mm,則在分離件剝離時會發生表面保護薄膜之浮凸。由比較例9可知,表面保護薄膜之彈性模數若在2.00×109 Pa以下,則於輸送中會產生皺褶。並且由比較例6及比較例7可知,分離件之厚度若小於35µm則輸送性會不足,而由比較例10可知,若分離件之厚度大於80µm,則在分離件剝離時會發生拾取不良。由比較例8可知,分離件之剝離力大於0.28N/25mm時,在剝離分離件時會發生拾取不良。 產業上之可利用性As is apparent from Table 1, the optical laminate of the embodiments of the present invention (especially Embodiment 1) has excellent transportability, and has excellent peelability of the surface protection film and the peelability of the separation piece. As can be seen from Comparative Example 1, if the thickness of the surface protection film is less than 40µm, the transportability will be insufficient. As can be seen from Comparative Examples 2 and 5, if the peeling force of the surface protection film is greater than 0.50N/25mm, delamination will occur when the surface protection film is peeled off, and as can be seen from Comparative Examples 3 and 4, if the peeling force of the surface protection film is less than 0.10N/25mm, embossing of the surface protection film will occur when the separation piece is peeled off. Comparative Example 9 shows that if the elastic modulus of the surface protection film is below 2.00×10 9 Pa, wrinkles will be generated during transportation. Comparative Examples 6 and 7 show that if the thickness of the separation piece is less than 35µm, the transportability will be insufficient, and Comparative Example 10 shows that if the thickness of the separation piece is greater than 80µm, poor picking will occur when the separation piece is peeled off. Comparative Example 8 shows that when the peeling force of the separation piece is greater than 0.28N/25mm, poor picking will occur when the separation piece is peeled off. Industrial Applicability
本發明之光學積層體可適用於影像顯示裝置。The optical multilayer body of the present invention can be applied to image display devices.
10:表面保護薄膜 20:偏光板 21:保護層 22:偏光件 30:黏著劑層 40:分離件 100:光學積層體10: Surface protection film 20: Polarizing plate 21: Protective layer 22: Polarizer 30: Adhesive layer 40: Separator 100: Optical laminate
圖1係本發明之一實施形態的光學積層體的概略截面圖。FIG1 is a schematic cross-sectional view of an optical laminate according to an embodiment of the present invention.
10:表面保護薄膜10: Surface protection film
20:偏光板20: Polarizing plate
21:保護層21: Protective layer
22:偏光件22: Polarizer
30:黏著劑層30: Adhesive layer
40:分離件40: Separation
100:光學積層體100: Optical multilayer
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| TW201930063A (en) * | 2017-10-31 | 2019-08-01 | 日商住友化學股份有限公司 | Laminate |
| TW201930064A (en) * | 2017-12-06 | 2019-08-01 | 日商日東電工股份有限公司 | Surface protective film and optical member with protective film |
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| JP5048120B2 (en) | 2010-03-31 | 2012-10-17 | 住友化学株式会社 | Method for producing polarizing laminated film and method for producing polarizing plate |
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| JP6138002B2 (en) * | 2013-09-09 | 2017-05-31 | 日東電工株式会社 | Polarizing film with adhesive layer for transparent conductive film, laminate, and image display device |
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| CN118778166A (en) * | 2019-08-21 | 2024-10-15 | 日东电工株式会社 | Optical laminate |
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| TW201930063A (en) * | 2017-10-31 | 2019-08-01 | 日商住友化學股份有限公司 | Laminate |
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