KR101518504B1 - Adhesive composition for polarizing plate, adhesive film comprising the same, polarizing plate comprising the same and optical display apparatus comprising the same - Google Patents
Adhesive composition for polarizing plate, adhesive film comprising the same, polarizing plate comprising the same and optical display apparatus comprising the same Download PDFInfo
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- KR101518504B1 KR101518504B1 KR1020130124259A KR20130124259A KR101518504B1 KR 101518504 B1 KR101518504 B1 KR 101518504B1 KR 1020130124259 A KR1020130124259 A KR 1020130124259A KR 20130124259 A KR20130124259 A KR 20130124259A KR 101518504 B1 KR101518504 B1 KR 101518504B1
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- South Korea
- Prior art keywords
- polarizing plate
- adhesive composition
- carbon atoms
- compound
- group
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- 239000000853 adhesive Substances 0.000 title claims abstract description 81
- 230000001070 adhesive effect Effects 0.000 title claims abstract description 79
- 239000000203 mixture Substances 0.000 title claims abstract description 78
- 239000002313 adhesive film Substances 0.000 title claims abstract description 14
- 230000003287 optical effect Effects 0.000 title abstract description 11
- 150000001875 compounds Chemical class 0.000 claims abstract description 55
- 239000003999 initiator Substances 0.000 claims abstract description 27
- 125000004432 carbon atom Chemical group C* 0.000 claims description 37
- -1 amine compound Chemical class 0.000 claims description 30
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical group [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims description 16
- 239000012790 adhesive layer Substances 0.000 claims description 14
- 229920001187 thermosetting polymer Polymers 0.000 claims description 10
- 239000012788 optical film Substances 0.000 claims description 9
- 125000001931 aliphatic group Chemical group 0.000 claims description 8
- 125000002029 aromatic hydrocarbon group Chemical group 0.000 claims description 8
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- 125000003545 alkoxy group Chemical group 0.000 claims description 5
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
- 125000003118 aryl group Chemical group 0.000 claims description 3
- 238000011065 in-situ storage Methods 0.000 claims description 3
- 238000000034 method Methods 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 125000004104 aryloxy group Chemical group 0.000 claims description 2
- 150000002431 hydrogen Chemical class 0.000 claims description 2
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- 230000000052 comparative effect Effects 0.000 description 16
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- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
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- 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 11
- 229920005989 resin Polymers 0.000 description 10
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- 238000012360 testing method Methods 0.000 description 6
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- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 2
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
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- 239000000654 additive Substances 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 2
- 239000004327 boric acid Substances 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 125000002091 cationic group Chemical group 0.000 description 2
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- 229910052740 iodine Inorganic materials 0.000 description 2
- 239000011630 iodine Substances 0.000 description 2
- PHQOGHDTIVQXHL-UHFFFAOYSA-N n'-(3-trimethoxysilylpropyl)ethane-1,2-diamine Chemical compound CO[Si](OC)(OC)CCCNCCN PHQOGHDTIVQXHL-UHFFFAOYSA-N 0.000 description 2
- 229920005668 polycarbonate resin Polymers 0.000 description 2
- 239000004431 polycarbonate resin Substances 0.000 description 2
- 229920001225 polyester resin Polymers 0.000 description 2
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- 229920000098 polyolefin Polymers 0.000 description 2
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- 238000007127 saponification reaction Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- JKUYRAMKJLMYLO-UHFFFAOYSA-N tert-butyl 3-oxobutanoate Chemical compound CC(=O)CC(=O)OC(C)(C)C JKUYRAMKJLMYLO-UHFFFAOYSA-N 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- WAKHLWOJMHVUJC-FYWRMAATSA-N (2e)-2-hydroxyimino-1,2-diphenylethanol Chemical compound C=1C=CC=CC=1C(=N/O)\C(O)C1=CC=CC=C1 WAKHLWOJMHVUJC-FYWRMAATSA-N 0.000 description 1
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 1
- IBDVWXAVKPRHCU-UHFFFAOYSA-N 2-(2-methylprop-2-enoyloxy)ethyl 3-oxobutanoate Chemical compound CC(=O)CC(=O)OCCOC(=O)C(C)=C IBDVWXAVKPRHCU-UHFFFAOYSA-N 0.000 description 1
- YLZOPXRUQYQQID-UHFFFAOYSA-N 3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)-1-[4-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]piperazin-1-yl]propan-1-one Chemical compound N1N=NC=2CN(CCC=21)CCC(=O)N1CCN(CC1)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F YLZOPXRUQYQQID-UHFFFAOYSA-N 0.000 description 1
- ZGLJYJVYUYQOHR-UHFFFAOYSA-N 3-oxobutanoyl 4-hydroxy-2-methylidenebutanoate Chemical compound CC(=O)CC(=O)OC(=O)C(=C)CCO ZGLJYJVYUYQOHR-UHFFFAOYSA-N 0.000 description 1
- LVNLBBGBASVLLI-UHFFFAOYSA-N 3-triethoxysilylpropylurea Chemical compound CCO[Si](OCC)(OCC)CCCNC(N)=O LVNLBBGBASVLLI-UHFFFAOYSA-N 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 229920002873 Polyethylenimine Polymers 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 1
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
- 150000001241 acetals Chemical class 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 239000002981 blocking agent Substances 0.000 description 1
- 230000005587 bubbling Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
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- 125000004122 cyclic group Chemical group 0.000 description 1
- 238000004042 decolorization Methods 0.000 description 1
- 238000007607 die coating method Methods 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
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- 239000010419 fine particle Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000007756 gravure coating Methods 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 150000002466 imines Chemical class 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 125000005647 linker group Chemical group 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- INJVFBCDVXYHGQ-UHFFFAOYSA-N n'-(3-triethoxysilylpropyl)ethane-1,2-diamine Chemical compound CCO[Si](OCC)(OCC)CCCNCCN INJVFBCDVXYHGQ-UHFFFAOYSA-N 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
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- 229920002492 poly(sulfone) Polymers 0.000 description 1
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- 229920000728 polyester Polymers 0.000 description 1
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- 239000005033 polyvinylidene chloride Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000002203 pretreatment Methods 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 238000004528 spin coating Methods 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- YRHRIQCWCFGUEQ-UHFFFAOYSA-N thioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3SC2=C1 YRHRIQCWCFGUEQ-UHFFFAOYSA-N 0.000 description 1
- ILJSQTXMGCGYMG-UHFFFAOYSA-N triacetic acid Chemical compound CC(=O)CC(=O)CC(O)=O ILJSQTXMGCGYMG-UHFFFAOYSA-N 0.000 description 1
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- 239000004034 viscosity adjusting agent Substances 0.000 description 1
Images
Classifications
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- 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
- C09J183/00—Adhesives based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon, with or without sulfur, nitrogen, oxygen, or carbon only; Adhesives based on derivatives of such polymers
- C09J183/04—Polysiloxanes
- C09J183/08—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen, and oxygen
-
- 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
- C09J7/20—Adhesives in the form of films or foils characterised by their carriers
- C09J7/22—Plastics; Metallised plastics
-
- 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
- C09J7/35—Heat-activated
-
- 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]
-
- 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
-
- 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
-
- 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
- G02F1/1303—Apparatus specially adapted to the manufacture of LCDs
-
- 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
- G02F1/1313—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 specially adapted for a particular application
-
- 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
- C09J2203/00—Applications of adhesives in processes or use of adhesives in the form of films or foils
- C09J2203/318—Applications of adhesives in processes or use of adhesives in the form of films or foils for the production of liquid crystal displays
-
- 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
- C09J2301/00—Additional features of adhesives in the form of films or foils
- C09J2301/30—Additional features of adhesives in the form of films or foils characterized by the chemical, physicochemical or physical properties of the adhesive or the carrier
- C09J2301/302—Additional features of adhesives in the form of films or foils characterized by the chemical, physicochemical or physical properties of the adhesive or the carrier the adhesive being pressure-sensitive, i.e. tacky at temperatures inferior to 30°C
-
- 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
- C09J2301/00—Additional features of adhesives in the form of films or foils
- C09J2301/30—Additional features of adhesives in the form of films or foils characterized by the chemical, physicochemical or physical properties of the adhesive or the carrier
- C09J2301/304—Additional features of adhesives in the form of films or foils characterized by the chemical, physicochemical or physical properties of the adhesive or the carrier the adhesive being heat-activatable, i.e. not tacky at temperatures inferior to 30°C
Landscapes
- Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- General Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Organic Chemistry (AREA)
- Nonlinear Science (AREA)
- Crystallography & Structural Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Polarising Elements (AREA)
Abstract
본 발명은 화학식 1의 화합물과 개시제를 포함하는 편광판용 접착제 조성물, 이를 포함하는 편광판용 접착 필름, 이를 포함하는 편광판 및 이를 포함하는 광학 표시 장치에 관한 것이다.The present invention relates to an adhesive composition for a polarizing plate comprising a compound of the formula (1) and an initiator, an adhesive film for a polarizing plate comprising the same, a polarizing plate including the same, and an optical display device comprising the same.
Description
본 발명은 편광판용 접착제 조성물, 이를 포함하는 편광판용 접착 필름, 이를 포함하는 편광판 및 이를 포함하는 광학 표시 장치에 관한 것이다.The present invention relates to an adhesive composition for a polarizing plate, an adhesive film for a polarizing plate containing the same, a polarizing plate including the same, and an optical display device including the same.
편광판은 폴리비닐알코올(PVA)계 편광자의 양면에 트리아세틸셀룰로스(TAC) 필름이 수계 접착제로 겹쳐 붙이거나 편면에 보호 필름 혹은 광학 보상 필름으로서 폴리에스테르계 수지, 폴리카보네이트계 수지, 아크릴계 수지, 비결정성 폴리올레핀계 수지나 시클로올레핀계 수지와 편면에 TAC 필름을 수계 접착제로 겹쳐 붙여서 제조하는 것이 일반적이다. TAC 필름은 투습도가 높아 수계 접착제를 사용하여 PVA계 편광자에 합지한 상태로 물을 건조시키면서 접착이 가능하다. 그러나 폴리에스테르계 수지, 폴리카보네이트계 수지, 아크릴계 수지, 비결정성 폴리올레핀계 수지나 시클로올레핀계 수지의 경우 TAC보다 소수성이거나 투습도가 낮기 때문에 수계 접착제를 이용하여 PVA계 편광자와 합지 시 잔류 수분이 남기 쉽고, 물이 남는다면 접착 강도 부족이나 외관 불량 등의 문제가 발생하게 된다. 상기와 같은 이유로, PVA계 편광자와 투습도가 낮은 보호필름을 합지하는 접착제로서 수계 접착제 대신 양이온 중합성 자외선 경화형 접착제를 사용하거나 열 경화형 접착제를 사용하는 것이 제안될 수 있다.(일본공개 2008-233874, 1997-022007).The polarizing plate may be formed by laminating a triacetyl cellulose (TAC) film on both sides of a polyvinyl alcohol (PVA) polarizer with an aqueous adhesive, or a protective film or an optical compensation film on one side of a polyester resin, a polycarbonate resin, It is common to produce a TAC film on one side with a polyolefin-based resin or a cycloolefin-based resin by using an aqueous adhesive. The TAC film has high moisture permeability and can be adhered to the PVA polarizer using water-based adhesive while drying the water. However, in the case of a polyester resin, a polycarbonate resin, an acrylic resin, an amorphous polyolefin resin or a cycloolefin resin, since the resin is hydrophobic or has a lower moisture permeability than TAC, residual moisture is likely to remain in the PVA- If the water remains, problems such as insufficient bonding strength and poor appearance may occur. For the above reasons, it is possible to use a cationic polymerizable ultraviolet curable adhesive instead of an aqueous adhesive or use a thermosetting adhesive as an adhesive for bonding a PVA polarizer and a protective film having a low moisture permeability. (Japanese Unexamined Patent Application Publication No. 2008-233874, 1997-022007).
그러나 편광판 제조시 자외선 경화형 접착제를 사용하는 경우, 편광판의 보호를 위해 보호필름에 자외선 차단제를 함께 사용하게 되고 이에 따라 충분한 자외선 조사가 이루어지지 않게 되어 접착강도 저하나 외관 불량 등이 발생하게 된다. 이를 위해 자외선 차단제가 사용되지 않는 보호필름 방향으로만 조사가 이루어져야 하는 등 작업성의 문제가 있다. 뿐만 아니라, 양이온 중합성 자외선 경화형 접착제는, 경화시의 습도의 영향을 받기 쉬우며, 경화 상태의 편차가 발생하기 쉽다는 문제로 인해 환경 습도는 물론, PVA계 편광자의 함수율을 엄격히 관리되는 등의 할 필요가 있다.However, when an ultraviolet curable adhesive is used in the production of a polarizing plate, an ultraviolet ray blocking agent is used together with the protective film for protection of the polarizing plate. As a result, sufficient ultraviolet ray irradiation is not performed and adhesive strength is lowered. For this, there is a problem of workability such that irradiation is required only in the direction of the protective film in which the ultraviolet screening agent is not used. In addition, the cationic polymerizable ultraviolet curing type adhesive is liable to be influenced by humidity at the time of curing and is liable to cause deviation in curing state, so that the moisture content of the PVA-based polarizer as well as the environmental humidity are strictly controlled Needs to be.
이에 반해 열 경화형 접착제에는, 이와 같은 문제가 비교적 적다는 점에서 우수하다. 열 경화형 접착제를 이용한 경우, 보호필름 자외선 차단 여부에 대한 제한이 없으며 환경 습도나 PVA계 편광자의 함수율에 대한 관리가 훨씬 용이하다.On the other hand, the thermosetting adhesive is excellent in that such a problem is relatively small. When a thermosetting adhesive is used, there is no restriction on whether the protective film is ultraviolet-shielded, and it is much easier to manage the environmental humidity or the moisture content of the PVA-based polarizer.
본 발명의 목적은 접착성, 응집성, 내구성이 높은 편광판용 접착제 조성물을 제공하는 것이다.An object of the present invention is to provide an adhesive composition for a polarizing plate having high adhesiveness, cohesiveness and durability.
본 발명의 다른 목적은 고온, 고습의 조건에서 편광자와 보호필름 간의 들뜸, 박리가 없게 할 수 있는 편광판용 접착제 조성물을 제공하는 것이다.Another object of the present invention is to provide an adhesive composition for a polarizing plate capable of preventing lifting and peeling between a polarizer and a protective film under high temperature and high humidity conditions.
본 발명의 또 다른 목적은 상기 편광판용 접착제 조성물로 형성된 접착필름을 제공하는 것이다.It is still another object of the present invention to provide an adhesive film formed of the adhesive composition for a polarizing plate.
본 발명의 또 다른 목적은 상기 편광판을 포함하는 광학 표시 장치를 제공하는 것이다.It is still another object of the present invention to provide an optical display device including the polarizing plate.
본 발명의 편광판용 접착제 조성물은 하기 화학식 1의 화합물과 개시제를 포함할 수 있다:The adhesive composition for a polarizing plate of the present invention may include a compound of the following formula (1) and an initiator:
<화학식 1>≪ Formula 1 >
(상기 화학식 1에서, R1, R2, R3, Ra, Rb, X1, X2, X3, m은 하기 상세한 설명에서 정의한 바와 같다).(Wherein R 1 , R 2 , R 3 , R a, R b, X 1 , X 2 , X 3 , m are as defined in the following description).
본 발명의 편광판용 접착 필름은 상기 편광판용 접착제 조성물로 형성될 수 있다.The adhesive film for a polarizing plate of the present invention may be formed of the adhesive composition for a polarizing plate.
본 발명의 편광판은 편광자; 상기 편광자의 일면 또는 양면에 형성된 광학필름; 및 상기 편광자와 상기 광학필름 사이에 형성된 접착제층을 포함하고, 상기 접착층은 상기 편광판용 접착제 조성물로 형성될 수 있다.The polarizer of the present invention comprises a polarizer; An optical film formed on one side or both sides of the polarizer; And an adhesive layer formed between the polarizer and the optical film, and the adhesive layer may be formed of the adhesive composition for a polarizing plate.
본 발명의 광학 표시 장치는 상기 편광판을 포함할 수 있다.The optical display device of the present invention may include the polarizing plate.
본 발명은 접착성, 응집성, 내구성이 높은 편광판용 접착제 조성물을 제공하였다. 본 발명은 고온, 고습의 조건에서 편광자와 보호필름 간의 들뜸, 박리가 없게 할 수 있는 편광판용 접착제 조성물을 제공하였다.The present invention provides an adhesive composition for a polarizing plate having high adhesiveness, cohesiveness and durability. The present invention provides an adhesive composition for a polarizing plate capable of preventing lifting and peeling between a polarizer and a protective film under high temperature and high humidity conditions.
도 1은 본 발명 일 실시예의 편광판의 단면도이다.
도 2는 본 발명 일 실시예의 광학 표시 장치의 단면도이다.1 is a sectional view of a polarizing plate of one embodiment of the present invention.
2 is a cross-sectional view of an optical display device according to an embodiment of the present invention.
본 명세서에서 '화합물'은 모노머, 올리고머, 수지 등을 포함할 수 있다.As used herein, the term " compound " may include monomers, oligomers, resins, and the like.
본 발명의 편광판용 접착제 조성물은 편광자의 일면 또는 양면에 광학필름을 접착하는데 사용될 수 있고, 상기 광학필름은 보호필름, 광학보상필름 중 하나 이상을 포함할 수 있다. 구체예에서, 상기 광학필름은 TAC(트리아세틸셀룰로오스), PET(폴리에틸렌테레프탈레이트), PC(폴리카보네이트), COP(시클릭올레핀폴리머), 아크릴 필름 등이 될 수 있지만, 이에 제한되지 않는다.The adhesive composition for a polarizing plate of the present invention may be used to adhere an optical film to one or both sides of a polarizer, and the optical film may include at least one of a protective film and an optical compensation film. In an embodiment, the optical film may be, but is not limited to, TAC (triacetylcellulose), PET (polyethylene terephthalate), PC (polycarbonate), COP (cyclic olefin polymer)
이하, 본 발명 일 실시예의 편광판용 접착제 조성물에 대해 설명한다.Hereinafter, the adhesive composition for a polarizing plate of one embodiment of the present invention will be described.
본 발명 일 실시예의 편광판용 접착제 조성물은 하기 화학식 1의 화합물을 포함할 수 있다:The adhesive composition for a polarizing plate of one embodiment of the present invention may comprise a compound of the following formula 1:
<화학식 1>≪ Formula 1 >
(상기 화학식 1에서, R1은 수소 또는 탄소수 1-3의 알킬기이고,(Wherein R 1 is hydrogen or an alkyl group having 1 to 3 carbon atoms,
R2는 탄소수 1-10의 지방족 탄화수소기 또는 탄소수 6-20의 방향족 탄화수소기이고,R 2 is an aliphatic hydrocarbon group having 1 to 10 carbon atoms or an aromatic hydrocarbon group having 6 to 20 carbon atoms,
R3은 수소, 탄소수 1-10의 지방족 탄화수소기 또는 탄소수 6-20의 방향족 탄화수소기이고,R 3 is hydrogen, an aliphatic hydrocarbon group having 1-10 carbon atoms or an aromatic hydrocarbon group having 6-20 carbon atoms,
Ra는 탄소수 1-10의 지방족 탄화수소기 또는 탄소수 6-20의 방향족 탄화수소기이고,Ra is an aliphatic hydrocarbon group having 1-10 carbon atoms or an aromatic hydrocarbon group having 6-20 carbon atoms,
Rb는 단일결합, 탄소수 1-10의 지방족 탄화수소기 또는 탄소수 6-20의 방향족 탄화수소기이고,Rb is a single bond, an aliphatic hydrocarbon group having 1-10 carbon atoms or an aromatic hydrocarbon group having 6-20 carbon atoms,
X1, X2, X3은 각각 독립적으로, 수산기, 탄소수 1-10의 알킬기, 탄소수 6-20의 아릴기, 탄소수 1-5의 알콕시기, 또는 탄소수 6-20의 아릴옥시기이고, X1, X2, X3 중 하나 이상은 수산기 또는 탄소수 1-5의 알콕시기이고,X 1 , X 2 and X 3 are each independently a hydroxyl group, an alkyl group having 1-10 carbon atoms, an aryl group having 6-20 carbon atoms, an alkoxy group having 1-5 carbon atoms, or an aryloxy group having 6-20 carbon atoms, X 1 , X 2 , and X 3 is a hydroxyl group or an alkoxy group having 1-5 carbon atoms,
m은 0 또는 1이다).m is 0 or 1).
구체예에서, R2는 탄소수 1-10의 알킬렌기 또는 탄소수 6-20의 아릴렌기, 예를 들면 탄소수 1-5의 알킬렌기가 될 수 있고, R3은 탄소수 1-10의 알킬기 또는 탄소수 6-20의 아릴기 예를 들면 탄소수 1-5의 알킬기가 될 수 있고, Ra는 탄소수 1-10의 알킬렌기 또는 탄소수 6-20의 아릴렌기 예를 들면 탄소수 1-5의 알킬렌기가 될 수 있고, Rb는 단일결합, 탄소수 1-10의 알킬렌기 또는 탄소수 6-20의 아릴렌기 예를 들면 단일 결합 또는 탄소수 1-5의 알킬렌기가 될 수 있고, X1, X2, X3은 탄소수 1-5의 알콕시기가 될 수 있다.In an embodiment, R 2 may be an alkylene group having 1 to 10 carbon atoms or an arylene group having 6 to 20 carbon atoms, for example, an alkylene group having 1 to 5 carbon atoms, R 3 is an alkyl group having 1 to 10 carbon atoms, An aryl group of 1 to 20 carbon atoms, for example, an alkyl group of 1 to 5 carbon atoms, Ra may be an alkylene group of 1 to 10 carbon atoms or an arylene group of 6 to 20 carbon atoms, , Rb is, for example, an arylene group of 6 to 20 carbon atoms in the alkylene group or a single bond, a carbon number of 1-10 and may be an alkylene group of a single bond or a carbon number of 1-5, X 1, X 2, X 3 is C 1 -5 < / RTI > alkoxy group.
화학식 1의 화합물은 편광판용 접착제 조성물에 포함되어, 편광판용 접착제 조성물의 접착성과 응집성을 높일 수 있고, 고온 및/또는 고습에서 편광자와 광학필름 간의 들뜸 및/또는 박리가 없게 할 수 있다. 또한, 화학식 1의 화합물은 열경화형 화합물로서, 편광판용 접착제 조성물에 포함되어, 광학필름의 자외선 차단 여부에 대한 제한이 없으며 환경 습도나 PVA계 편광자의 함수율에 대한 관리가 훨씬 용이하게 할 수 있다.The compound of the formula (1) is contained in the adhesive composition for a polarizing plate, so that the adhesiveness and cohesiveness of the adhesive composition for a polarizing plate can be enhanced and there is no lifting and / or peeling between the polarizer and the optical film at high temperature and / or high humidity. The compound of the formula (1) is a thermosetting compound which is contained in an adhesive composition for a polarizing plate, so that there is no restriction on whether the optical film is shielded from ultraviolet rays, and the humidity and the moisture content of the PVA polarizer can be controlled much more easily.
화학식 1의 화합물은 중량평균분자량이 400 내지 800g/mol이 될 수 있고, 상기 범위에서 편광판용 접착제 조성물은 낮은 점도를 가져 젖음성 효과가 있을 수 있다. 화학식 1의 화합물은 25℃에서 점도가 50 내지 150cPs가 될 수 있고, 상기 범위에서, 균일한 두께의 편광판용 접착층을 형성할 수 있다.The compound of the formula (1) may have a weight average molecular weight of 400 to 800 g / mol, and the adhesive composition for a polarizing plate in the above range may have a low viscosity and a wettability effect. The compound of formula (1) may have a viscosity of 50 to 150 cPs at 25 占 폚, and within this range, an adhesive layer for a polarizing plate having a uniform thickness can be formed.
화학식 1의 화합물은 고형분 기준 편광판용 접착제 조성물 중 1-50중량%, 예를 들면 10-50중량% 또는 5-30중량%로 포함될 수 있고, 상기 범위에서, 편광판용 접착제 조성물은 낮은 점도 및 경화 후 응집성이 높아지는 효과가 있을 수 있다.The compound of formula (I) may be contained in an amount of 1-50 wt%, for example, 10-50 wt% or 5-30 wt% of the adhesive composition for a polarizing plate based on a solid content, There is an effect that the post-cohesion property is increased.
화학식 1의 화합물은 상업적으로 판매되는 제품을 사용할 수 있고, 또는 실란기 함유 아민 화합물 및 라디칼 경화형 화합물로부터 제조될 수 있는데, 구체적으로는 실란기 함유 아민 화합물의 아민기와 라디칼 경화형 화합물의 아세토아세톡시기의 반응에 의해 제조될 수 있다.The compound of formula (1) may be a commercially available product or may be prepared from a silane group-containing amine compound and a radical-curing compound. Specifically, the amine group of the silane group-containing amine compound and the acetoacetoxy group of the radical- ≪ / RTI >
구체예에서, 실란기 함유 아민 화합물은 실란기 및 1개의 아민기를 함유하는 단관능 아민 화합물, 또는 실란기 및 2개 이상의 아민기를 함유하는 다관능 아민 화합물을 포함할 수 있다. 일 구체예에서, 실란기 아민 화합물은 하기 화학식 2로 표시될 수 있다:In an embodiment, the silane group-containing amine compound may include a monofunctional amine compound containing a silane group and an amine group, or a polyfunctional amine compound containing a silane group and two or more amine groups. In one embodiment, the silane group amine compound may be represented by the following formula:
<화학식 2>(2)
(상기 화학식 2에서, Ra, Rb, X1, X2, X3, m은 상기에서 정의한 바와 같다).(Ra, Rb, X 1 , X 2 , X 3 , and m are as defined above).
구체적으로, 실란기 아민 화합물은 3-ureidopropyltriethoxysilane, N-(2-aminoethyl)-3-aminopropyltriethoxysilane, 하기 화학식 2a의 화합물 중 하나 이상을 포함할 수 있고, 이들은 단독 또는 2종 이상 배합하여 사용될 수 있다:Specifically, the silane group amine compound may include at least one of 3-ureidopropyltriethoxysilane, N- (2-aminoethyl) -3-aminopropyltriethoxysilane, and a compound of the following formula (2a), and these may be used alone or in combination of two or more.
<화학식 2a>≪ EMI ID =
구체예에서, 라디칼 경화형 화합물은 하기 화학식 3의 관능기(예:아세토아세톡시기)를 갖는 라디칼 경화성 화합물을 포함할 수 있다:In embodiments, the radical curable compound may include a radical curable compound having a functional group of the following formula (e.g., acetoacetoxy group):
<화학식 3>(3)
(상기 화학식 3에서 *은 연결기이고, R3은 상기에서 정의한 바와 같다)(Wherein * is a linking group and R 3 is as defined above)
예를 들면, 라디칼 경화형 화합물은 하기 화학식 4로 표시될 수 있다:For example, the radical curable compound may be represented by the following formula (4): < EMI ID =
<화학식 4>≪ Formula 4 >
(상기 화학식 4에서, R1, R2, R3은 상기에서 정의한 바와 같다).(Wherein R 1 , R 2 and R 3 are as defined above).
예를 들면, 라디칼 경화성 화합물은 아세토아세톡시에틸 (메타)아크릴레이트, 아세토아세톡시메틸 (메타)아크릴레이트, 아세토아세톡시프로필 (메타)아크릴레이트, 아세토아세톡시부틸 (메타)아크릴레이트 중 하나 이상을 포함할 수 있고, 이들은 단독 또는 2종 이상 배합하여 사용될 수 있다.For example, the radical-curable compound may be at least one of acetoacetoxyethyl (meth) acrylate, acetoacetoxymethyl (meth) acrylate, acetoacetoxypropyl (meth) acrylate, and acetoacetoxybutyl These may be used alone or in combination of two or more.
실란기 함유 아민 화합물 및 라디칼 경화형 화합물의 반응은 통상의 방법으로 수행될 수 있다. 예를 들면 실란기 함유 아민 화합물과 라디칼 경화형 화합물을 1:20 내지 1:1 중량비로 혼합하고 상온에서 반응시킬 수 있으며, 개시제를 더 포함시켜 반응시킬 수도 있다. 개시제는 광경화 개시제, 열경화 개시제, 또는 이들의 혼합물을 포함할 수 있고, 라디칼 경화형 화합물 100중량부에 대해 0.1 내지 3중량부로 포함될 수 있고, 상기 범위에서 반응이 충분히 진행될 수 있고, 잔량의 개시제가 남아 투명도 저하를 막을 수 있다.The reaction of the silane group-containing amine compound and the radical curing compound can be carried out by a conventional method. For example, the silane group-containing amine compound and the radical curing compound may be mixed at a weight ratio of 1:20 to 1: 1 and reacted at room temperature. The initiator may include a photo-curing initiator, a thermal curing initiator, or a mixture thereof. The initiator may be included in an amount of 0.1 to 3 parts by weight based on 100 parts by weight of the radical-curable compound, So that the decrease in transparency can be prevented.
편광판용 접착제 조성물은 개시제를 더 포함할 수 있다.The adhesive composition for a polarizing plate may further include an initiator.
개시제는 화학식 1의 화합물을 경화시킴으로써, 편광판용 접착제 조성물의 응집성과 접착력을 높일 수 있다. 개시제는 광경화 개시제, 열경화 개시제, 또는 이들의 혼합물을 포함할 수 있다. 따라서, 편광판용 접착제 조성물은 광경화형 또는 열경화형 접착제 조성물일 수 있다.By curing the compound of the formula (1), the initiator can increase the cohesiveness and adhesion of the adhesive composition for a polarizing plate. The initiator may include a photo-curing initiator, a thermal curing initiator, or a mixture thereof. Accordingly, the adhesive composition for a polarizing plate may be a photocurable or thermosetting adhesive composition.
광경화 개시제는 인계, 트리아진계, 아세토페논계, 벤조페논계, 티오크산톤계, 벤조인계, 옥심계 또는 이들의 혼합물을 포함할 수 있다. 열경화 개시제는 퍼옥시계 화합물, 아조계 화합물, 케탈계 화합물, 헤미케탈계 화합물, 또는 이들의 혼합물을 포함할 수 있다. 바람직하게는, 개시제는 열경화 개시제가 될 수 있다. 접착제 조성물은 열 경화 개시제를 포함함으로써, 광경화 개시제 사용시 문제가 될 수 있는 보호필름에 의한 자외선 차단의 제한이 없고, 습도나 편광자의 함수율에 대한 관리를 용이하게 할 수 있다.The photocuring initiator may include phosphorus, triazine, acetophenone, benzophenone, thioxanthone, benzoin, oxime, or a mixture thereof. The thermoset initiator may include a peroxide clock compound, an azo-based compound, a ketal-based compound, a hemi-ketal-based compound, or a mixture thereof. Preferably, the initiator may be a thermal curing initiator. Since the adhesive composition contains a thermosetting initiator, there is no restriction of the ultraviolet shielding by the protective film which may be a problem when using the photo-curing initiator, and the humidity and the water content of the polarizer can be easily managed.
개시제는 화학식 1의 화합물 100중량부에 대하여 0.1-6중량부로 포함될 수 있다. 상기 범위에서, (메타)아크릴레이트 화합물의 중합이 충분히 될 수 있고 잔량의 개시제가 남는 것을 막을 수 있다. 바람직하게는 0.1-3중량부로 포함될 수 있다.The initiator may be included in an amount of 0.1 to 6 parts by weight based on 100 parts by weight of the compound of formula (1). Within this range, the polymerization of the (meth) acrylate compound can be sufficiently carried out and the remaining amount of the initiator can be prevented from remaining. Preferably 0.1-3 parts by weight.
개시제는 고형분 기준 상기 조성물 중 0.1-2중량%, 바람직하게는 1-2중량%로 포함될 수 있다. 상기 범위에서, 열경화 후 신뢰성 안정화 효과가 있을 수 있다.The initiator may be contained in an amount of from 0.1 to 2% by weight, preferably from 1 to 2% by weight, based on the solid content of the composition. Within the above range, there may be a reliability stabilizing effect after thermosetting.
편광판용 접착제 조성물은 본 발명의 효과를 손상시키지 않는 범위에서, 산화 방지제, 자외선 흡수제, 이온계 도전제, 도전성 금속 산화물 미립자 등의 도전성 부여 첨가제, 광확산성 부여 첨가제, 점도 조절제 등을 포함할 수 있다.The adhesive composition for a polarizing plate may contain a conductivity-imparting additive such as an antioxidant, an ultraviolet absorber, an ion-type conductive agent, and a conductive metal oxide fine particle, a light diffusivity-imparting additive, a viscosity modifier, and the like within a range that does not impair the effect of the present invention have.
편광판용 접착제 조성물은 상술한 성분을 배합한 것으로, 25℃ 점도는 150cPs 미만이 될 수 있다. 상기 범위에서, 접착제 조성물의 도공성이 좋을 수 있다. 바람직하게는 점도는 1-135cPs, 더 바람직하게는 40-100cPs가 될 수 있다.The adhesive composition for a polarizing plate is blended with the components described above, and the viscosity at 25 ° C may be less than 150 cPs. Within the above range, the coating property of the adhesive composition may be good. Preferably, the viscosity may be 1-135 cPs, more preferably 40-100 cPs.
편광판용 접착제 조성물은 도포가 잘되도록 하기 위해 용제를 포함할 수 있지만, 용제를 포함하지 않는 무용제 타입으로 함으로써 기포 발생 등의 문제점을 해소할 수 있다.The adhesive composition for a polarizing plate may contain a solvent to facilitate application, but it is possible to solve problems such as bubbling by using a solventless type solvent-free adhesive composition.
구체예에서, 편광판용 접착제 조성물은 실란기 함유 아민 화합물, 라디칼 경화형 화합물을 반응시켜 화학식 1의 화합물을 제조하고, in situ(인 시투)로 개시제를 혼합하여 제조할 수도 있다. 이때, 조성물은 화학식 1의 화합물과 개시제뿐만 아니라, 실란기 함유 아민 화합물, 라디칼 경화형 화합물 중 하나 이상을 더 포함할 수 있고, 실란기 함유 아민 화합물은 기재와의 접착 향상 효과를 구현할 수 있고, 라디칼 경화형 화합물은 고온/고습 신뢰성 조건에서 내구성 향상 효과를 구현할 수 있다. 예를 들면, 조성물 중 실란기 함유 아민 화합물은 5-50중량%, 라디칼 경화형 화합물은 30-95중량% 예를 들면 50-95중량%로 포함될 수 있다.In embodiments, the adhesive composition for a polarizing plate is by reacting a silane-group-containing amine compound, a radical-curable compound to prepare a compound of formula 1, in situ (in situ). < / RTI > At this time, the composition may further include at least one of a silane group-containing amine compound and a radical-curing compound, as well as the compound of the formula (1) and the initiator, and the silane group- The curing compound can realize durability improvement effect under high temperature / high humidity reliability condition. For example, the silane group-containing amine compound in the composition may be contained in an amount of 5-50% by weight, and the radical curing compound in an amount of 30-95% by weight, for example, 50-95% by weight.
예를 들면 조성물은 고형분 기준으로 화학식 1의 화합물 5-30중량%, 실란기 함유 아민 화합물 5-10중량%, 라디칼 경화형 화합물 50-85중량%, 개시제 0.1-1중량%를 포함할 수 있다. 상기 범위에서, 젖음성이 높아지는 효과가 있을 수 있다. 또한, 조성물은 고형분 기준으로 화학식 1의 화합물 5-50중량%, 라디칼 경화형 화합물 30-94중량% 예를 들면 30-50중량% 예를 들면 49-94중량%, 개시제 0.1-1중량%를 포함할 수 있다. 상기 범위에서, 신뢰성 향상 효과가 있을 수 있다.For example, the composition may include 5-30 wt% of the compound of Formula 1, 5-10 wt% of the silane group-containing amine compound, 50-85 wt% of the radical curing compound, and 0.1-1 wt% of the initiator based on the solid content. Within this range, there may be an effect of increasing the wettability. In addition, the composition comprises 5-50% by weight of the compound of formula 1, 30-94% by weight of the radical curing compound, for example, 30-50% by weight, for example 49-94% by weight and 0.1-1% can do. In the above range, reliability can be improved.
본 발명의 편광판용 접착 필름은 상기 편광판용 접착제 조성물로 형성될 수 있고, 편광판용 접착 필름은 편광자와 보호필름의 접착에 사용될 수 있다. The adhesive film for a polarizing plate of the present invention may be formed of an adhesive composition for a polarizing plate, and an adhesive film for a polarizing plate may be used for bonding the polarizing film and the protective film.
편광판용 접착 필름의 두께는 0.1㎛-5㎛, 바람직하게는 0.1-1㎛가 될 수 있다. 상기 범위에서, 편광판용 접착 필름으로 사용할 수 있다.The thickness of the polarizing plate adhesive film may be 0.1 占 퐉 to 5 占 퐉, preferably 0.1-1 占 퐉. In the above range, it can be used as an adhesive film for a polarizing plate.
편광판용 접착 필름은 편광판용 접착제 조성물을 경화시켜 제조할 수 있다. 일 구체예에서, 경화는 80℃ 이상, 바람직하게는 80-150℃에서 수행될 수 있다. 다른 구체예에서, 경화는 10-2000mW/cm2, 10-2000J/cm2의 조건으로 수행될 수 있다. The adhesive film for a polarizing plate can be produced by curing an adhesive composition for a polarizing plate. In one embodiment, the curing can be carried out at 80 占 폚 or higher, preferably 80-150 占 폚. In other embodiments, curing may be carried out under the conditions of 10-2000mW / cm 2, 10-2000J / cm 2.
본 발명의 편광판은 상기 편광판용 접착제 조성물로 형성된 접착제층을 포함할 수 있다. The polarizing plate of the present invention may include an adhesive layer formed of the adhesive composition for a polarizing plate.
도 1은 본 발명의 일 실시예의 편광판 단면도이다. 도 1을 참조하면, 편광판(100)은 편광자(10), 편광자(10)의 상부에 형성된 제1보호필름(20), 편광자(10)의 하부에 형성된 제2보호필름(30)을 포함하고, 제1보호필름(20)과 편광자(10) 사이에는 제1접착제층(40)이 형성되어 있고, 제2보호필름(30)과 편광자(10) 사이에는 제2접착제층(50)이 형성되어 있고, 제1접착제층(40)과 제2접착층(50) 중 하나 이상은 본 발명 실시예의 편광판용 접착제 조성물로 형성될 수 있다.1 is a cross-sectional view of a polarizer of an embodiment of the present invention. 1, the
편광자는 폴리비닐알코올계 수지로 된 필름으로부터 제조될 수 있다. 폴리비닐알코올계 수지로는 폴리비닐알코올, 폴리비닐포르말, 폴리비닐아세탈 또는 에틸렌 초산 비닐 공중합체의 검화물 등을 사용할 수 있다. 폴리비닐알코올계 수지로 된 필름의 검화도는 99mol% 이상, 바람직하게는 99-99.5mol%, 중합도는 2000 이상, 바람직하게는 2000-2500, 두께는 10㎛-200㎛가 될 수 있다.The polarizer can be produced from a film made of a polyvinyl alcohol-based resin. As the polyvinyl alcohol-based resin, polyvinyl alcohol, polyvinyl formal, polyvinyl acetal, or a saponified product of an ethylene-vinyl acetate copolymer can be used. The degree of saponification of the film made of the polyvinyl alcohol-based resin may be 99 mol% or more, preferably 99-99.5 mol%, the degree of polymerization may be 2000 or more, preferably 2000-2500, and the thickness may be 10 탆 to 200 탆.
편광자는 폴리비닐알코올계 수지로 된 필름에 요오드를 염착시키고, 연신하여 제조될 수 있다. 연신비는 2.0-6.0이 될 수 있다. 연신 후, 붕산 용액과 요오드화 칼륨 수용액의 침지 과정에 의한 색 보정 단계를 거칠 수도 있다.The polarizer can be produced by dying iodine to a film made of a polyvinyl alcohol-based resin and stretching it. The stretching ratio may be 2.0-6.0. After stretching, the color correction step may be performed by immersing the boric acid solution and the aqueous potassium iodide solution.
편광자의 두께는 10㎛-200㎛가 될 수 있고, 상기 범위에서 편광판에 사용될 수 있다.The thickness of the polarizer may be 10 占 퐉 to 200 占 퐉, and may be used for the polarizer in the above range.
보호필름은 편광자의 일면 또는 양면에 적층되는 것으로, 편광판의 용도에 적합하도록 투명한 필름이라면 특별히 제한되지 않는다. 구체예로서, 트리아세틸셀룰로스(TAC)를 포함하는 셀룰로오스계, 폴리에틸렌테레프탈레이트(PET)를 포함하는 폴리에스테르계, 고리형 폴리올레핀(COP)계, 폴리카보네이트(PC)계, 폴리아크릴레이트계, 폴리에테르술폰계, 폴리술폰계, 폴리아미드계, 폴리이미드계, 폴리올레핀계, 폴리아릴레이트계, 폴리비닐알코올계, 폴리염화비닐계, 폴리염화비닐리덴계 또는 이들의 혼합으로 이루어진 군으로부터 선택되는 재질로 된 필름일 수 있다.The protective film is laminated on one surface or both surfaces of the polarizer, and is not particularly limited as long as it is a transparent film suitable for the use of the polarizing plate. As a concrete example, there can be mentioned cellulose-based materials including triacetylcellulose (TAC), polyester-based materials including polyethylene terephthalate (PET), cyclic polyolefin (COP) -based materials, polycarbonate (PC) A material selected from the group consisting of an ether sulfone type, a polysulfone type, a polyamide type, a polyimide type, a polyolefin type, a polyarylate type, a polyvinyl alcohol type, a polyvinyl chloride type, a polyvinylidene chloride type, Lt; / RTI >
보호필름은 25㎛-500㎛의 두께를 가질 수 있다. 상기 범위에서, 편광 소자에 적층시 편광판으로 사용할 수 있다. 바람직하게는 25㎛-100㎛의 두께를 가질 수 있다.The protective film may have a thickness of 25 占 퐉 to 500 占 퐉. In the above range, it can be used as a polarizing plate when laminated on a polarizing element. And preferably 25 占 퐉 to 100 占 퐉.
보호필름은 접착제 조성물의 도포 전 또는 편광판 제조 전에 표면 처리, 예를 들면 250mJ/cm2 이상 코로나 전처리 단계를 거칠 수도 있다.The protective film may be subjected to a surface treatment, for example, a corona pre-treatment step of 250 mJ / cm 2 or more before the application of the adhesive composition or before the preparation of the polarizing plate.
접착제층은 상기 편광판용 접착제 조성물로 형성될 수 있다. 접착제층의 두께는 0.1㎛-5㎛가 될 수 있다.The adhesive layer may be formed of the adhesive composition for the polarizing plate. The thickness of the adhesive layer may be 0.1 占 퐉 to 5 占 퐉.
편광판은 통상의 방법으로 제조할 수 있다. 예를 들면, 보호필름 한쪽 면에 편광판용 접착제 조성물을 도포하여, 접착제 조성물 층을 갖는 보호필름을 제조한다. 필요에 따라 건조 등을 행할 수 있다. 도포 방법으로는 예를 들면 다이 코팅법, 롤 코팅법, 그라비아 코팅법, 스핀 코팅법을 사용할 수 있다. 상기 접착제 조성물 층을 갖는 보호필름을 편광자의 상면 및 하면 각각에 적층하여 적층체를 얻는다. 접착제 조성물 층을 경화시킴으로써 접착제층을 형성하고, 이로부터 편광판을 제조한다. 상기 접착제 조성물의 경화는 상술한 방법에 의할 수 있다.The polarizing plate can be produced by a conventional method. For example, an adhesive composition for a polarizing plate is applied to one side of a protective film to produce a protective film having an adhesive composition layer. Drying and the like can be carried out if necessary. As the coating method, for example, a die coating method, a roll coating method, a gravure coating method and a spin coating method can be used. A protective film having the above-mentioned adhesive composition layer is laminated on each of the upper and lower surfaces of the polarizer to obtain a laminate. The adhesive composition layer is cured to form an adhesive layer, from which a polarizing plate is produced. The curing of the adhesive composition may be carried out by the method described above.
본 발명의 광학 표시 장치는 상기 편광판 접착제 조성물, 상기 접착제 조성물로 형성된 접착제층, 또는 이를 포함하는 편광판을 포함할 수 있다. 광학 표시 장치는 편광판이 포함되는 통상의 광학 표시 장치로 예를 들면 액정 디스플레이, 유기발광소자 디스플레이 등을 포함할 수 있다.The optical display device of the present invention may include the polarizer adhesive composition, the adhesive layer formed of the adhesive composition, or a polarizer including the same. The optical display device may be a conventional optical display device including a polarizing plate, for example, a liquid crystal display, an organic light emitting diode display, or the like.
도 2는 본 발명 일 구체예의 액정 디스플레이의 단면도이다. 2 is a cross-sectional view of a liquid crystal display according to an embodiment of the present invention.
도 2를 참조하면, 본 발명 일 실시예의 액정 디스플레이는 액정 디스플레이 패널(200); 및 액정 디스플레이 패널(200)의 상부에 형성된 편광판(100)을 포함하고, 편광판(100)은 본 발명 일 실시에의 접착제 조성물로 형성된 접착필름을 포함할 수 있다. 도 2에는 도시되지 않았지만, 액정 디스플레이 패널의 하부에는 편광판이 더 포함될 수 있고, 상기 편광판은 상기 접착제 조성물로 형성된 접착필름을 포함할 수 있다.2, the liquid crystal display of one embodiment of the present invention includes a liquid
본 명세서에서, '상부'와 '하부'는 도면을 기준으로 정의한 것으로, 보는 시각에 따라 '상부'가 '하부'로 '하부'가 '상부'로 변경될 수 있다.In the present specification, 'upper' and 'lower' are defined with reference to drawings, and 'upper' may be changed to 'lower' and 'lower' may be changed to 'upper' according to viewing time.
이하, 실시예를 통하여 본 발명을 보다 구체적으로 설명하고자 하나, 이러한 실시예들은 단지 설명의 목적을 위한 것으로 본 발명을 제한하는 것으로 해석되어서는 안 된다.Hereinafter, the present invention will be described in more detail by way of examples, but these examples are for illustrative purposes only and should not be construed as limiting the present invention.
하기 실시예와 비교예에서 사용된 성분의 구체적인 사양은 다음과 같다.Specific specifications of the components used in the following examples and comparative examples are as follows.
A.실란기 함유 아민 화합물:N-(2-아미노에틸)-3-아미노프로필트리메톡시실란(신에츠화학공업주식회사, 상품명: KBM-603)A. Amine compound containing silane group: N- (2-aminoethyl) -3-aminopropyltrimethoxysilane (Shin-Etsu Chemical Co., Ltd., trade name: KBM-603)
B.라디칼 경화형 화합물:2-아세토아세톡시에틸 아크릴레이트(Eastman, 상품명:AAEM)B. Radical curable compound: 2-acetoacetoxyethyl acrylate (Eastman, trade name: AAEM)
C.개시제:벤조일 퍼옥시드(일본, 유자社)C. Initiator: benzoyl peroxide (Yuzawa, Japan)
D.이민계 화합물:폴리에틸렌이민(일본합성, 상품명:SP-012)D. Immune compound: polyethyleneimine (trade name: SP-012)
E.(메타)아크릴레이트 함유하지 않는 화합물:1,1-디메틸에틸-3-옥소부타노에이트(Eastman, 상품명 : TBAA)E. Compound not containing (meth) acrylate: 1,1-dimethylethyl-3-oxobutanoate (Eastman, trade name: TBAA)
실시예Example 1 One
용제 없이 (A), (B)를 하기 표 1(단위:중량부)에 기재된 함량으로 배합하여 하기 화학식 1a의 화합물이 제조되었음을 NMR 등으로 확인하고, (C)개시제를 2중량부 배합하고 믹싱하여 편광판용 접착제 조성물을 제조하였다.(A) and (B) were blended in the contents described in Table 1 (unit: parts by weight) without solvent to confirm that the compound of formula (1a) was prepared by NMR and 2 parts by weight of the initiator (C) To prepare an adhesive composition for a polarizing plate.
<화학식 1a><Formula 1a>
실시예Example 2 내지 4 2 to 4
실시예 1에서 (A),(B)의 함량을 하기 표 1과 같이 변경한 것을 제외하고는 실시예 1과 동일한 방법으로, 편광판용 접착제 조성물을 제조하였다. An adhesive composition for a polarizing plate was prepared in the same manner as in Example 1, except that the contents of (A) and (B) in Example 1 were changed as shown in Table 1 below.
비교예Comparative Example 1 내지 4 1 to 4
실시예 1에서 (A),(B),(D),(E)의 함량을 하기 표 1과 같이 변경한 것을 제외하고는 실시예 1과 동일한 방법으로, 편광판용 접착제 조성물을 제조하였다.An adhesive composition for a polarizing plate was prepared in the same manner as in Example 1, except that the contents of (A), (B), (D) and (E) were changed as shown in Table 1 in Example 1.
편광판의 제조Production of Polarizer
편광자 제조를 위한 필름으로 80 ㎛ 두께의 폴리비닐알코올 필름(검화도:99.5, 중합도:2000)을 사용하였다. 폴리비닐알코올 필름을 0.3% 요오드 수용액에 침지시켜 염착한 후, 연신배율이 5.0이 되도록 연신하였다. 이어서 연신된 폴리비닐알코올 필름을 3% 농도의 붕산 용액과 2% 요오드화 칼륨 수용액에 침지시켜 색상 보정을 한 후, 50 ℃에서 4분간 건조하여 편광자를 제조하였다.A polyvinyl alcohol film (degree of saponification: 99.5, degree of polymerization: 2000) having a thickness of 80 mu m was used as a film for polarizer production. The polyvinyl alcohol film was immersed in an aqueous 0.3% iodine solution, and then stretched to give a stretch ratio of 5.0. Subsequently, the stretched polyvinyl alcohol film was immersed in a boric acid solution of 3% concentration and an aqueous solution of 2% potassium iodide to perform color correction, followed by drying at 50 DEG C for 4 minutes to prepare a polarizer.
투명 제1보호필름으로 80㎛ 두께의 트리아세테이트 셀룰로오스(TAC)를 사용하였으며, 250 mJ/㎠ 이상 코로나 처리를 하였다.As the first transparent protective film, 80 mu m thick triacetate cellulose (TAC) was used and subjected to corona treatment at 250 mJ / cm < 2 > or more.
투명 제2보호필름으로 30㎛ 두께의 시클로올레핀계 수지는, 환상 올레핀을 중합 단위로 하여 중합되는 수지를 총칭(COP)를 사용하였고, 250 mJ/㎠ 이상 코로나 처리를 하였다.As a transparent second protective film, a cycloolefin resin having a thickness of 30 탆 was subjected to a corona treatment using a resin which was polymerized with cyclic olefin as a polymerization unit, and which was generically referred to as COP, at a rate of 250 mJ / cm 2 or more.
온도 22~25℃, 습도 20~60% 환경 하에서 제1보호필름 - 접착제 조성물 - 편광자 - 접착제 조성물 - 제2보호필름의 순서로 합지하고, 80℃ 오븐에서 5분 동안 건조시켜 편광판을 제조하였다.The first protective film-adhesive composition-polarizer-adhesive composition-second protective film under the environment of a temperature of 22 to 25 ° C and a humidity of 20 to 60%, and dried in an oven at 80 ° C for 5 minutes to prepare a polarizing plate.
실시예와 비교예의 편광판용 접착제 조성물 또는 편광판에 대하여 하기의 물성을 평가하고 표 2에 나타내었다.The following properties of the adhesive composition or polarizing plate for a polarizing plate of Examples and Comparative Examples were evaluated and shown in Table 2.
(1)열충격 크랙 발생 개수: 실시예 및 비교예에서 제조된 편광판의 열충격 조건 하 Crack 수준을 알아보기 위해 100mm x 100mm(가로 x 세로)으로 편광필름 제조 후 Glass에 Lamination 시켜 시료를 준비한다. -40℃ ~ 85℃ 100 cycle 열충격 방치 후 샘플을 형광등 아래의 반사 모드 및 Back Light 모드에서 MD 방향으로의 편광자 Crack이 발생하였는지를 확인하여 그 개수를 측정하였다. 전체 시험 편광판의 개수는 5개이었다.(1) Number of heat shock cracks: The polarizing plate prepared in Examples and Comparative Examples was laminated to glass after preparing a polarizing film with a size of 100 mm x 100 mm (width x length) in order to examine the crack level under thermal shock condition. -40 ° C to 85 °
(2)접착성: 편광판용 접착 필름의 접착성을 확인하기 위해서 편광판의 단부의 보호필름과 편광자의 사이에 커터 칼끝을 삽입하였다. 칼끝이 보호필름과 편광자 사이에 들어가지 않는 것을 ◎, 칼끝이 조금 들어간 것은 ○, 칼끝이 조금 들어갔지만 일정한 강도가 있어 도중에 보호필름이 찢어진 것을 △, 칼끝이 용이하게 들어 간 것을 X로 평가하여 측정결과는 표에 나타내었다.(2) Adhesiveness: In order to confirm the adhesiveness of the polarizing plate adhesive film, a cutter cutter was inserted between the protective film at the end of the polarizing plate and the polarizer. The edge of the protective film did not enter the gap between the protective film and the polarizer, the edge of the edge of the edge was slightly inclined, the edge of the edge of the edge was slightly inclined, The results are shown in the table.
(3)온수 침지 시험(내구성): 상기 제조된 편광판을 가로 X 세로가 5cm X 5cm가 되도록 샘플을 만든다. 항온수(60℃) 중에 2시간 동안 각각 침지시켰다. 편광자의 탈색 여부와 편광자 일 말단의 수축 길이의 최고값을 측정하였다. 수축 길이는 온수 침지 시험 후 편광판에 있어서 보호 필름 말단에서부터 인접한 편광자 말단까지의 거리 중 최소값을 의미한다. 보호 필름은 내수성 테스트에서 수축하지 않지만, 편광자는 온수에 침지시 수축된다. 편광자가 박리 및 탈색되지 않은 것을 ◎, 편광자가 0mm 초과 1mm 이하 박리되고 탈색된 것 ○, 편광자가 1mm 초과 2mm 이하 박리되고 탈색된 것을 △, 편광자가 2mm 초과 박리되고 탈색된 것을 X로 평가하였다.(3) Hot water immersion test (durability): A sample is prepared so that the polarizing plate prepared above has a width X length of 5 cm X 5 cm. And immersed in constant temperature water (60 DEG C) for 2 hours, respectively. The highest values of the decolorization of the polarizer and the contraction length of the one end of the polarizer were measured. The shrinkage length means the minimum value of the distance from the end of the protective film to the end of the polarizer adjacent to the polarizer after the hot water immersion test. The protective film does not shrink in the water resistance test, but the polarizer shrinks when immersed in hot water. A polarizer was peeled off and not discolored.?, A polarizer was peeled off from 1 mm or less to 1 mm or less.?, A polarizer was peeled from 1 mm or more to 2 mm or less and peeled off?
(4)접착제 조성물의 점도:Viscometer(모델명: DV-Ⅱ+Pro, Broolfield사 제조)를 이용하여 접착제 조성물의 25℃ 점도를 측정하였다. (4) Viscosity of adhesive composition: The viscosity of the adhesive composition at 25 캜 was measured using a Viscometer (Model: DV-II + Pro, manufactured by Broolfield).
(25℃, cPs)Viscosity
(25 C, cPs)
상기 표 2에서 나타난 바와 같이, 본 발명의 편광판용 접착제 조성물은 접착성이 좋고, 온수 침지시에도 편광자와 보호필름이 박리되거나 탈색되지 않아 내구성이 좋고, 열충격에도 크랙이 발생 개수가 현저하게 낮았다.As shown in Table 2, the adhesive composition for a polarizing plate of the present invention has good adhesiveness and is excellent in durability because the polarizer and protective film are not peeled off or discolored even in hot water immersion, and the number of cracks is remarkably low even in thermal shock.
반면에, 화학식 1의 화합물을 포함하지 않고 실란기 함유 아민 화합물을 포함하는 비교예 1은 크랙 발생 빈도가 높고 내구성, 접착성도 좋지 않았다. 또한, 화학식 1의 화합물을 포함하지 않고 라디칼 경화형 화합물을 포함하는 비교예 2는 기재와의 접착이 이루어지지 않는 문제점이 있었다. 또한, 본 발명의 라디칼 경화형 화합물과 구조가 유사하지만 (메타)아크릴레이트기를 포함하지 않는 화합물을 포함하는 비교예 3은 접착성과 내구성이 문제가 되었다. 또한, 종래 수계 접착제의 성분인 이민계 화합물을 포함하는 비교예 4는 편광자와 보호필름간에 합지가 되지 않았다.On the other hand, Comparative Example 1 containing the silane group-containing amine compound without the compound of the formula (1) had a high occurrence frequency of cracking, and was not durable and adhesive. In addition, in Comparative Example 2, which does not include the compound of Formula 1 and contains a radical-curing compound, there is a problem that adhesion with the substrate is not achieved. Also, in Comparative Example 3, which contains a compound similar in structure to the radical curable compound of the present invention but does not contain a (meth) acrylate group, adhesion and durability became a problem. Further, in Comparative Example 4 including an imine compound which is a component of the conventional water-based adhesive, no gap was formed between the polarizer and the protective film.
본 발명의 단순한 변형 내지 변경은 이 분야의 통상의 지식을 가진 자에 의하여 용이하게 실시될 수 있으며, 이러한 변형이나 변경은 모두 본 발명의 영역에 포함되는 것으로 볼 수 있다. It will be understood by those skilled in the art that various changes in form and details may be made therein without departing from the spirit and scope of the invention as defined by the appended claims.
Claims (15)
<화학식 1>
(상기 화학식 1에서, R1은 수소 또는 탄소수 1-3의 알킬기이고,
R2는 탄소수 1-10의 지방족 탄화수소기 또는 탄소수 6-20의 방향족 탄화수소기이고,
R3은 수소, 탄소수 1-10의 지방족 탄화수소기 또는 탄소수 6-20의 방향족 탄화수소기이고,
Ra는 탄소수 1-10의 지방족 탄화수소기 또는 탄소수 6-20의 방향족 탄화수소기이고,
Rb는 단일결합, 탄소수 1-10의 지방족 탄화수소기 또는 탄소수 6-20의 방향족 탄화수소기이고,
X1, X2, X3은 각각 독립적으로 수산기, 탄소수 1-10의 알킬기, 탄소수 6-20의 아릴기, 탄소수 1-5의 알콕시기, 탄소수 6-20의 아릴옥시기이고,
X1, X2, X3 중 하나 이상은 수산기 또는 탄소수 1-5의 알콕시기이고,
m은 0 또는 1이다).An adhesive composition for a polarizing plate comprising a compound of the following formula (1) and an initiator:
≪ Formula 1 >
(Wherein R 1 is hydrogen or an alkyl group having 1 to 3 carbon atoms,
R 2 is an aliphatic hydrocarbon group having 1 to 10 carbon atoms or an aromatic hydrocarbon group having 6 to 20 carbon atoms,
R 3 is hydrogen, an aliphatic hydrocarbon group having 1-10 carbon atoms or an aromatic hydrocarbon group having 6-20 carbon atoms,
Ra is an aliphatic hydrocarbon group having 1-10 carbon atoms or an aromatic hydrocarbon group having 6-20 carbon atoms,
Rb is a single bond, an aliphatic hydrocarbon group having 1-10 carbon atoms or an aromatic hydrocarbon group having 6-20 carbon atoms,
X 1 , X 2 and X 3 each independently represent a hydroxyl group, an alkyl group having 1-10 carbon atoms, an aryl group having 6-20 carbon atoms, an alkoxy group having 1-5 carbon atoms, or an aryloxy group having 6-20 carbon atoms,
At least one of X 1 , X 2 and X 3 is a hydroxyl group or an alkoxy group having from 1 to 5 carbon atoms,
m is 0 or 1).
<화학식 2>
(상기 화학식 2에서, Ra, Rb, X1, X2, X3, m은 상기에서 정의한 바와 같다).6. The adhesive composition for a polarizing plate according to claim 5, wherein the silane group-containing amine compound is represented by the following formula (2)
(2)
(Ra, Rb, X 1 , X 2 , X 3 , and m are as defined above).
<화학식 4>
(상기 화학식 4에서, R1, R2, R3은 상기에서 정의한 바와 같다).6. The adhesive composition for a polarizing plate according to claim 5, wherein the radical-curable compound is represented by the following formula (4)
≪ Formula 4 >
(Wherein R 1 , R 2 and R 3 are as defined above).
상기 접착제층은 제1항 내지 제12항 중 어느 한 항의 편광판용 접착제 조성물로 형성된 편광판.A polarizer; An optical film formed on one side or both sides of the polarizer; And an adhesive layer formed between the polarizer and the optical film,
Wherein the adhesive layer is formed of the adhesive composition for a polarizing plate according to any one of claims 1 to 12.
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Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
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KR100393405B1 (en) | 1993-07-14 | 2003-07-31 | 롬 앤드 하스 캄파니 | A Process for producing functional monomer via enamine of acetoacetate |
US7812090B2 (en) | 2006-06-02 | 2010-10-12 | Valspar Sourcing, Inc. | High performance aqueous coating compositions |
WO2013147192A1 (en) | 2012-03-30 | 2013-10-03 | 日東電工株式会社 | Polarized film, optical film, and image display device |
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2013
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Publication number | Priority date | Publication date | Assignee | Title |
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KR100393405B1 (en) | 1993-07-14 | 2003-07-31 | 롬 앤드 하스 캄파니 | A Process for producing functional monomer via enamine of acetoacetate |
US7812090B2 (en) | 2006-06-02 | 2010-10-12 | Valspar Sourcing, Inc. | High performance aqueous coating compositions |
WO2013147192A1 (en) | 2012-03-30 | 2013-10-03 | 日東電工株式会社 | Polarized film, optical film, and image display device |
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