WO2011062127A1 - 偏光板用粘着剤組成物およびこれを利用した偏光板 - Google Patents
偏光板用粘着剤組成物およびこれを利用した偏光板 Download PDFInfo
- Publication number
- WO2011062127A1 WO2011062127A1 PCT/JP2010/070260 JP2010070260W WO2011062127A1 WO 2011062127 A1 WO2011062127 A1 WO 2011062127A1 JP 2010070260 W JP2010070260 W JP 2010070260W WO 2011062127 A1 WO2011062127 A1 WO 2011062127A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- sensitive adhesive
- pressure
- polarizing plate
- adhesive composition
- mass
- Prior art date
Links
Classifications
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B5/00—Optical elements other than lenses
- G02B5/30—Polarising elements
-
- C—CHEMISTRY; METALLURGY
- 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
- C09J133/00—Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Adhesives based on derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/62—Polymers of compounds having carbon-to-carbon double bonds
- C08G18/6216—Polymers of alpha-beta ethylenically unsaturated carboxylic acids or of derivatives thereof
- C08G18/625—Polymers of alpha-beta ethylenically unsaturated carboxylic acids; hydrolyzed polymers of esters of these acids
- C08G18/6254—Polymers of alpha-beta ethylenically unsaturated carboxylic acids and of esters of these acids containing hydroxy groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/77—Polyisocyanates or polyisothiocyanates having heteroatoms in addition to the isocyanate or isothiocyanate nitrogen and oxygen or sulfur
- C08G18/78—Nitrogen
- C08G18/79—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates
- C08G18/791—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates containing isocyanurate groups
- C08G18/794—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates containing isocyanurate groups formed by oligomerisation of aromatic isocyanates or isothiocyanates
-
- 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
- C09J11/00—Features of adhesives not provided for in group C09J9/00, e.g. additives
- C09J11/02—Non-macromolecular additives
- C09J11/06—Non-macromolecular additives organic
-
- 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
- C09J133/00—Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Adhesives based on derivatives of such polymers
- C09J133/04—Homopolymers or copolymers of esters
- C09J133/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
- C09J133/08—Homopolymers or copolymers of acrylic acid esters
-
- 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
- C09J175/00—Adhesives based on polyureas or polyurethanes; Adhesives based on derivatives of such polymers
- C09J175/04—Polyurethanes
-
- 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
- C09J7/38—Pressure-sensitive adhesives [PSA]
- C09J7/381—Pressure-sensitive adhesives [PSA] based on macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- C09J7/385—Acrylic polymers
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/0025—Crosslinking or vulcanising agents; including accelerators
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/29—Compounds containing one or more carbon-to-nitrogen double bonds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3467—Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
- C08K5/3477—Six-membered rings
- C08K5/3492—Triazines
- C08K5/34924—Triazines containing cyanurate groups; Tautomers thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L63/00—Compositions of epoxy resins; Compositions of derivatives of epoxy resins
-
- 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
- C09J2301/40—Additional features of adhesives in the form of films or foils characterized by the presence of essential components
- C09J2301/408—Additional features of adhesives in the form of films or foils characterized by the presence of essential components additives as essential feature of the adhesive layer
Definitions
- the present invention relates to a pressure-sensitive adhesive composition for polarizing plates, and more specifically, a pressure-sensitive adhesive composition for polarizing plates capable of forming a pressure-sensitive adhesive layer with excellent optical suitability by aging for a short period of time and polarized light using the same. It is about a board.
- the liquid crystal element has a structure in which a liquid crystal material is sandwiched between two substrates, and a polarizing plate is attached to the surface of the substrate via an adhesive layer.
- the polarizing plate has a multi-layered structure of different materials and has poor dimensional stability due to the characteristics of the constituent materials.
- stress concentrates due to the contraction of the polarizing plate and induces birefringence of the polarizing plate.
- Color unevenness occurs at the concentrated end, and the display quality deteriorates.
- problems such as foaming at the interface between the polarizing plate and glass and peeling of the polarizing plate are likely to occur. Therefore, excellent light leakage prevention and durability are required for the pressure-sensitive adhesive for polarizing plates.
- Patent Document 1 a method of promoting curing by adding a carboxyl group to the hydroxyl group-containing acrylic polymer in a mixture of the hydroxyl group-containing acrylic polymer and the isocyanate-based crosslinking agent has been proposed (Patent Document 1).
- Patent Document 1 a method of promoting curing by adding a carboxyl group to the hydroxyl group-containing acrylic polymer in a mixture of the hydroxyl group-containing acrylic polymer and the isocyanate-based crosslinking agent has been proposed (Patent Document 1).
- Patent Document 1 a method of promoting curing by adding a carboxyl group to the hydroxyl group-containing acrylic polymer in a mixture of the hydroxyl group-containing acrylic polymer and the isocyanate-based crosslinking agent
- a pressure-sensitive adhesive composition for a surface protective film which comprises an acrylic polymer containing a hydroxyl group and a carboxyl group, and an aliphatic or alicyclic polyfunctional isocyanate or isocyanurate compound, and has a shortened curing period Is disclosed (Patent Document 2).
- the acrylic polymer used in this pressure-sensitive adhesive composition has a limited amount of carboxyl groups and is not suitable for use in bonding a polarizing plate and glass. If the above aliphatic or alicyclic polyfunctional isocyanate or isocyanurate compound is added to an adhesive having 1 part or more of the carboxyl group of the present invention, the pot life tends to be shortened and It could not be used.
- Patent Documents 3 and 4 a pressure-sensitive adhesive composition for an optical film in which an isocyanate compound is added to an acrylic polymer having a carboxyl group is disclosed.
- Patent Documents 3 and 4 aim to improve reworkability and light leakage prevention properties, and do not consider any shortening of the ripening period. Therefore, none of the pressure-sensitive adhesive compositions disclosed in these documents can obtain sufficient optical suitability by aging for a short time.
- JP 2008-156513 A Japanese Patent Laid-Open No. 2005-247909 Japanese Patent No. 4136524 JP 2008-144126 A
- a pressure-sensitive adhesive composition for a polarizing plate capable of forming a pressure-sensitive adhesive layer having excellent durability and light leakage prevention properties by short-term aging is desired, and the present invention provides such a pressure-sensitive adhesive for a polarizing plate.
- An object of the present invention is to provide an agent composition.
- the present inventors used a tolylene diisocyanate compound having an isocyanurate structure as a crosslinking agent, and converted this into a carboxyl group-containing acrylic polymer having a molecular weight in a specific range.
- the present inventors have found that a pressure-sensitive adhesive layer having excellent durability and light leakage prevention property can be formed even by aging for a short time by blending in a relatively large amount.
- the present invention The following components (A) and (B) (A) 100 parts by weight of a (meth) acrylic polymer having a weight average molecular weight of 300,000 to 1,500,000 obtained by copolymerizing at least 1 to 10% by weight of a carboxyl group-containing monomer (B) Tolylene diisocyanate having an isocyanurate structure
- a pressure-sensitive adhesive composition for polarizing plates comprising 4 to 20 parts by mass of a system compound.
- this invention is a polarizing plate which provides the adhesive layer formed from the said adhesive composition for polarizing plates on the at least one surface of a polarizing film.
- the pressure-sensitive adhesive composition of the present invention is used for a polarizing plate to effectively prevent the occurrence of light leakage even under high temperature and high humidity conditions, and has excellent durability, and the pressure-sensitive adhesive layer is foamed or peeled off. Etc. can be suppressed. Furthermore, since the curing speed is fast and the aging period can be greatly shortened, productivity can be significantly improved and the amount of inventory can be reduced.
- the acrylic polymer of component (A) used in the pressure-sensitive adhesive composition for polarizing plates of the present invention is obtained by copolymerizing at least a carboxyl group-containing monomer.
- carboxyl group-containing monomer examples include (meth) acrylic acid, 2-carboxyethyl (meth) acrylate, 3-carboxypropyl (meth) acrylate, 4-carboxybutyl (meth) acrylate, itaconic acid, crotonic acid, maleic acid, Examples thereof include fumaric acid and maleic anhydride.
- the content of the carboxyl group-containing monomer with respect to the total constituent monomers of the component (A) acrylic polymer is 1 to 10% by mass (hereinafter referred to as “%”), preferably 2 to 8%, more preferably 2 ⁇ 6%. If it is less than 1%, it is difficult to obtain a cohesive force, and if it is more than 10%, it is not preferable because the cohesive force is too high or the adhesive force is increased.
- constituent monomers of the acrylic polymer of component (A) include (meth) acrylic acid alkyl ester, hydroxyl group-containing monomer, benzene ring-containing monomer, (meth) acrylic acid alkoxy ester, amino group-containing monomer, amide-containing monomer, etc. Is mentioned.
- the (meth) acrylic acid alkyl ester those having an alkyl group having 1 to 12 carbon atoms which may be branched are preferable. Specifically, methyl (meth) acrylate, ethyl (meth) acrylate, propyl ( (Meth) acrylate, isopropyl (meth) acrylate, butyl (meth) acrylate, isobutyl (meth) acrylate, pentyl (meth) acrylate, hexyl (meth) acrylate, 2-ethylhexyl (meth) acrylate, octyl (meth) acrylate, nonyl ( Examples include meth) acrylate, decyl (meth) acrylate, dodecyl (meth) acrylate, and lauryl (meth) acrylate. Of these, butyl acrylate and methyl acrylate are preferably used because of a good balance between adhesive strength and durability.
- Component (A) The content of the (meth) acrylic acid alkyl ester with respect to the entire constituent monomers of the acrylic polymer is 10 to 99%, preferably 50 to 98.5%. If it is less than 10%, the adhesive force and durability may not be balanced, and if it exceeds 99%, durability may be deteriorated.
- Examples of the hydroxyl group-containing monomer include 2-hydroxyethyl (meth) acrylate, 4-hydroxybutyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate, 2-hydroxybutyl (meth) acrylate, and 6-hydroxyhexyl (meth).
- Examples include acrylate, 1,4-cyclohexanedimethanol mono (meth) acrylate, chloro-2-hydroxypropyl acrylate, diethylene glycol mono (meth) acrylate, allyl alcohol, and the like. The fraction can be made higher.
- 2-hydroxyethyl acrylate and 4-hydroxybutyl acrylate are preferably used because of good copolymerizability with the (meth) acrylic acid alkyl ester.
- Component (A) The content of the hydroxyl group-containing monomer with respect to the entire constituent monomers of the acrylic polymer is 0 to 1%, preferably 0.05 to 1%. If it exceeds 1%, the gel fraction becomes too high, the adhesiveness is lowered, and peeling or the like may occur under high temperature and high humidity heat conditions.
- the above benzene ring-containing monomer has positive intrinsic birefringence, and the birefringence of the (meth) acrylic polymer can be reduced by copolymerizing the monomer.
- benzyl acrylate and phenoxyethyl acrylate are preferably used because they have good compatibility and copolymerization with (meth) acrylic acid alkyl esters and do not deteriorate transparency.
- Component (A) The content of the benzene ring-containing monomer with respect to the entire constituent monomers of the acrylic polymer is 0 to 40%, preferably 0 to 30%. If it is more than 40%, an appropriate adhesive strength may not be obtained.
- Examples of the (meth) acrylic acid alkoxyester include 2-methoxyethyl (meth) acrylate, 2-ethoxyethyl (meth) acrylate, 2-methoxypropyl (meth) acrylate, and 3-methoxypropyl (meth) acrylate.
- Examples include 2-methoxybutyl (meth) acrylate and 4-methoxybutyl (meth) acrylate.
- the content of the (meth) acrylic acid alkoxy ester with respect to the entire constituent monomer of the component (A) acrylic polymer is 0 to 90%, preferably 0 to 80%.
- amino group-containing monomer examples include dimethylaminoethyl (meth) acrylate and diethylaminoethyl (meth) acrylate.
- amide-containing monomer examples include (meth) acrylamide, (meth) N-methylolacrylamide and the like. These amino group-containing monomers and amide group-containing monomers are used in an amount of about 0 to 1% with respect to the total constituent monomers of the component (A) acrylic polymer.
- the component (A) of the present invention can be produced by polymerizing a mixture of the above monomer components by a conventionally known polymerization method such as a solution polymerization method, a bulk polymerization method, an emulsion polymerization method or a suspension polymerization method.
- a conventionally known polymerization method such as a solution polymerization method, a bulk polymerization method, an emulsion polymerization method or a suspension polymerization method.
- a polymerization stabilizer such as an emulsifier and a suspending agent are more preferable.
- the weight average molecular weight (Mw) of the component (A) obtained as described above is 300,000 to 1,500,000, preferably 400,000 to 1,200,000.
- the weight average molecular weight is less than 300,000, the durability is deteriorated.
- the weight average molecular weight is more than 1,500,000, the viscosity is increased, resulting in a problem in handling.
- a weight average molecular weight means the value calculated
- the acrylic polymer of component (A) preferably has a glass transition temperature of 0 ° C. or lower, more preferably ⁇ 20 ° C. or lower, and particularly preferably ⁇ 80 to ⁇ 30 ° C.
- the glass transition temperature is a value calculated by the following FOX equation.
- the tolylene diisocyanate compound having an isocyanurate structure of component (B) used in the present invention is a compound containing an isocyanurate ring formed by trimerization of tolylene diisocyanate in its structure, and includes various modified products. Is done.
- the compound of component (B) can be obtained by the method described in JP-A-8-193114 and International Publication No. 2006/137307, and the compounds corresponding to component (B) include coronate 342 and coronate 2030 ( Both are made by Nippon Polyurethane Industry Co., Ltd.).
- the compounding amount of the component (B) in the pressure-sensitive adhesive composition for polarizing plates of the present invention is 4 to 20 parts, preferably 6 with respect to 100 parts by mass (hereinafter referred to as “parts”) of the component (A). ⁇ 15 parts.
- parts parts by mass
- crosslinking agent other than the above component (B) can be used in combination with the pressure-sensitive adhesive composition for polarizing plates of the present invention (component (C)).
- crosslinking agents include tolylene diisocyanate crosslinking agents (excluding those having an isocyanurate structure), epoxy crosslinking agents, and aziridine crosslinking agents. One or more of these may be used. it can.
- Examples of the tolylene diisocyanate-based crosslinking agent include tolylene diisocyanate and isocyanate compounds obtained by subjecting this to a polyhydric alcohol such as trimethylolpropane and pentaerythritol, burette type compounds, May include derivatives such as urethane prepolymer type isocyanate compounds obtained by addition reaction with known polyether polyols, polyester polyols, acrylic polyols, polybutadiene polyols, polyisoprene polyols and the like.
- a polyhydric alcohol such as trimethylolpropane and pentaerythritol, burette type compounds
- May include derivatives such as urethane prepolymer type isocyanate compounds obtained by addition reaction with known polyether polyols, polyester polyols, acrylic polyols, polybutadiene polyols, polyisoprene polyols and the like.
- tolylene diisocyanate crosslinking agent excluding those having an isocyanurate structure
- the adhesion to the substrate can be improved and peeling and the like can be suppressed.
- tolylene diisocyanate, trimethylolpropane tolylene diisocyanate, and the like are preferable.
- the tolylene diisocyanate crosslinking agent (excluding those having an isocyanurate structure) is blended so that the blending ratio with respect to the component (B) is 1: 3 to 3: 1. It is preferable to do. If the blending ratio is outside this range, aging takes a long time, and peeling may occur under high temperature and high humidity heat conditions.
- epoxy crosslinking agent examples include bisphenol A epichlorohydrin type epoxy resin, ethylene diglycidyl ether, polyethylene glycol diglycidyl ether, glycerin diglycidyl ether, glycerin triglycidyl ether, 1,6-hexanediol diglycidyl ether, trimethylolpropane.
- triglycidyl ether diglycidyl aniline, diamine glycidyl amine, N, N, N ′, N′-tetraglycidyl-m-xylylenediamine, 1,3-bis (N, N′-diamine glycidylaminomethyl) cyclohexane, etc.
- Examples thereof include compounds having two or more epoxy groups in the molecule.
- these epoxy-based crosslinking agents in combination, the gel fraction can be further increased.
- N, N, N ′, N′-tetraglycidyl-m-xylylenediamine, 1,3-bis (N, N′-diamine glycidylaminomethyl) cyclohexane is preferably used.
- the blending amount of the epoxy crosslinking agent in the pressure-sensitive adhesive composition for polarizing plates of the present invention is 0 to 1%, preferably 0.05 to 0.5%, relative to the component (B). If the blending amount is out of this range, aging takes a long time, and peeling may occur under high temperature and high humidity heat conditions.
- aziridine-based crosslinking agent examples include 1,1 ′-(methylene-di-p-phenylene) bis-3,3-aziridylurea, 1,1 ′-(hexamethylene) bis-3,3-aziridylurea, Examples include 4,6-triaziridinyl-1,3,5-triazine, trimethylolpropane-tris- (2-aziridinylpropionate), and the like.
- the blending amount of the aziridine-based crosslinking agent in the pressure-sensitive adhesive composition for polarizing plates of the present invention is 0 to 1%, preferably 0.05 to 0.5%, relative to the component (B). If the blending amount is out of this range, the aging period becomes long, and peeling may occur under high temperature and high humidity heat conditions.
- the pressure-sensitive adhesive composition for polarizing plate of the present invention it is preferable to further blend a silane coupling agent (D) containing a group that reacts with a carboxyl group contained in the acrylic polymer of component (A).
- a silane coupling agent (D) containing a group that reacts with a carboxyl group contained in the acrylic polymer of component (A).
- the pressure-sensitive adhesive can be firmly adhered to the glass, and peeling can be prevented in a humid heat environment.
- an amino group-containing silane coupling agent such as 3-aminopropyltrimethoxysilane and N-2 (aminoethyl) 3-aminopropyltrime
- the compounding amount of the silane coupling agent (D) in the pressure-sensitive adhesive composition for polarizing plates of the present invention is 0.05-1 part, preferably 0.1-0. 5 parts. If it is less than 0.05 part, peeling is likely to occur in a moist heat environment, and if it is more than 1 part, the silane coupling agent bleeds in a high temperature environment, and conversely, peeling is liable to occur.
- the pressure-sensitive adhesive composition for polarizing plates of the present invention is prepared by blending the above components (A) and (B) with components (C) and (D) and other optional components as necessary, and mixing them according to a conventional method. Is done by.
- optional components include antioxidants, ultraviolet absorbers, plasticizers, antistatic agents, and the like, and these can be blended as long as the effects of the present invention are not impaired.
- the pressure-sensitive adhesive composition was applied to at least one surface on the support according to a conventional method, and after coating, Dry and mature to form an adhesive layer. Drying is usually performed at 80 to 110 ° C. for about 2 to 10 minutes.
- the pressure-sensitive adhesive composition of the present invention can significantly shorten the aging period as compared with the conventional ones.
- the pressure-sensitive adhesive composition can be sufficiently ripened for about 1 to 3 days at 23 ° C. and 50% RH. Curing is performed, and an adhesive layer having good adhesive strength and optical suitability is obtained.
- the gel fraction of the pressure-sensitive adhesive layer after aging is preferably 60 to 90%, more preferably 65 to 85%. If it is outside this range, the durability may be inferior and the film may be easily peeled off.
- a gel fraction means the value calculated
- a polyester film having a surface peel-treated can be used as the support.
- the thickness of the pressure-sensitive adhesive layer is usually about 10 to 30 ⁇ m, preferably about 15 to 25 ⁇ m.
- the polarizing plate of the present invention can be obtained by providing an adhesive layer formed from the above-mentioned adhesive composition for polarizing plates on at least one surface of the polarizing film.
- the thickness of the pressure-sensitive adhesive layer provided on the polarizing film is usually about 10 to 30 ⁇ m, preferably about 15 to 25 ⁇ m.
- the pressure-sensitive adhesive composition is applied on the polarizing film, dried and matured, or the coated and dried coating on the support is laminated on the polarizing film, An adhesive layer can be formed by aging this.
- the conditions for drying and aging, the range of the gel fraction, and the like are the same as described above.
- polarizing film used in the present invention layers having other functions may be laminated, and specifically, an elliptically polarizing film, a retardation film and the like are included.
- a liquid crystal element is manufactured by providing the polarizing plate of the present invention obtained as described above on the substrate surface of a liquid crystal cell.
- the type of liquid crystal element in which the polarizing plate of the present invention is used is not particularly limited, and may be any of TN mode, VA mode, IPS mode, OCB mode, and the like.
- a liquid crystal display device with reduced light leakage is manufactured by appropriately attaching components such as a backlight to the liquid crystal element.
- the polarizing plate pressure-sensitive adhesive composition of the present invention can form a pressure-sensitive adhesive layer having excellent light leakage prevention properties and durability by aging for a short period of time.
- the reason is considered as follows. That is, when an excessive amount of an isocyanate compound is added to the pressure-sensitive adhesive, it is said that polyurea derived from the isocyanate compound is produced. This polyurea is entangled with the main polymer of the pressure-sensitive adhesive to form a physical bond, and has the same stitch structure as that of a general pressure-sensitive adhesive. However, the same entanglement occurs in the case of a tolylene diisocyanate compound having an isocyanurate structure. It is considered to have a mesh structure.
- the polyurea derived from the tolylene diisocyanate compound having an isocyanurate structure is highly elastic and can also control birefringence, so that the light leakage prevention property is good, and the tolylene diisocyanate compound having an isocyanurate structure is Since the reactivity is high compared with other isocyanate compounds and the crosslinking reaction and polyurea formation reaction are fast, it is considered that the aging period can be greatly shortened.
- Acrylic polymer production In a flask equipped with a stirrer, a nitrogen gas inlet tube, a thermometer and a reflux condenser, 97 parts by mass of butyl acrylate, 3 parts by mass of acrylic acid, 100 parts by mass of ethyl acetate, 0.04 parts by mass of normal dodecyl mercaptan (NDM) The contents of the flask were heated to 60 ° C. while introducing nitrogen gas into the charged flask. Next, 0.1 part by mass of a polymerization initiator azobisisobutyronitrile (AIBN) sufficiently substituted with nitrogen gas was added to the flask under stirring.
- AIBN polymerization initiator azobisisobutyronitrile
- Measuring device HLC-8120GPC (manufactured by Tosoh Corporation)
- GPC column configuration The following five columns (all manufactured by Tosoh Corporation) (1) TSK-GEL HXL-H (guard column) (2) TSK-GEL G7000HXL (3) TSK-GEL GMHXL (4) TSK-GEL GMHXL (5) TSK-GEL G2500HXL Diluted with tetrahydrofuran so that the sample concentration is 1.0 mg / cm 3
- Mobile phase solvent Tetrahydrofuran Flow rate: 1 ml / min Column temperature: 40 ° C
- Nonvolatile content 100 x [weight after heating (n3-n1) / weight before heating (n2-n1)]
- Production examples 2-6 Acrylic polymer A2 to A6 solutions were obtained in the same manner as in Production Example 1 except that the monomer composition shown in Table 1 was used. Mw, Mn, nonvolatile content and viscosity of this polymer were measured in the same manner as in Production Example 1. The results are shown in Table 1.
- Comparative production example 1-4 Acrylic polymer B1-B4 solutions were obtained in the same manner as in Production Example 1 except that the monomer composition shown in Table 1 was used. Mw, Mn, nonvolatile content and viscosity of this polymer were measured in the same manner as in Production Example 1. The results are shown in Table 1.
- Example 1 Production of polarizing plate having an adhesive layer: (Preparation of adhesive composition) Coronate 342 (manufactured by Nippon Polyurethane Co., Ltd.), a tolylene diisocyanate (TDI) -based isocyanurate modified product, with respect to 100 parts by mass of the acrylic polymer A1 (solid content) of the acrylic polymer A1 solution obtained in Production Example 1. 5 parts by mass and 0.2 part by mass of KBM-403 (manufactured by Shin-Etsu Chemical Co., Ltd.) as a silane coupling agent were added, and these were sufficiently mixed to obtain an adhesive composition.
- Coronate 342 manufactured by Nippon Polyurethane Co., Ltd.
- TDI tolylene diisocyanate
- KBM-403 manufactured by Shin-Etsu Chemical Co., Ltd.
- Examples 2-12 A pressure-sensitive adhesive composition was obtained in the same manner as in Example 1 except that the acrylic polymer and the crosslinking agent were changed as shown in Table 2 below. Moreover, the polarizing plate which has an adhesive layer was produced like Example 1 using the obtained adhesive composition.
- Comparative Examples 1-11 A pressure-sensitive adhesive composition was obtained in the same manner as in Example 1 except that the acrylic polymer and the crosslinking agent were changed as shown in Table 3 below. Moreover, the polarizing plate which has an adhesive layer was produced like Example 1 using the obtained adhesive composition.
- Test example 1 Of the polarizing plates obtained in Examples 1 to 12 and Comparative Examples 1 to 11, those having an aging period of 1 day and 7 days were evaluated for durability and light leakage prevention property by the following methods. These results are summarized in Tables 2 and 3.
- ⁇ Durability evaluation method> A polarizing plate having an adhesive layer is cut into a size of 150 mm ⁇ 250 mm, stuck on one side of a glass plate using a laminator roll, and then held in an autoclave adjusted to 50 ° C. and 5 atm for 20 minutes.
- a test plate was prepared. Two similar test plates were prepared and left for 500 hours under conditions of a temperature of 60 ° C. and a humidity of 95% RH (moisture and heat resistance) and a temperature of 85 ° C. (heat resistance). Were visually observed and evaluated. (Standard) ⁇ : Foaming, peeling, cracks are not seen ⁇ : Foaming, peeling, cracks are slightly seen ⁇ : Foaming, peeling, cracks are seen over the entire surface
- Test example 2 For the polarizing plates having the adhesive layers of aging 1, 3, and 7 obtained in Examples 1 to 12 and Comparative Examples 1 to 11, the adhesive strength was evaluated by the following method. In addition, the pressure-sensitive adhesive layers formed from the pressure-sensitive adhesive compositions obtained in Examples 1 to 12 and Comparative Examples 1 to 11 were evaluated for gel fractions at aging days 1, 3, and 7 by the following method. These results are shown in Table 4.
- a polarizing plate having an adhesive layer was cut into a size of 70 mm ⁇ 25 mm to prepare a test piece. After peeling the polyester film from the test piece and sticking it on one side of the glass plate using a laminator roll, it was held in an autoclave adjusted to 50 ° C. and 5 atm for 20 minutes. Next, after being left for 1 hour in an environment of 23 ° C. and 50% RH, the film was pulled at a speed of 300 mm / min in the 90 ° direction, and the peel strength was measured.
- the pressure-sensitive adhesive composition of the present invention is a pressure-sensitive adhesive that effectively prevents light leakage by aging for a short period of time, has excellent durability, and can suppress the occurrence of foaming or peeling even under high temperature and high humidity conditions.
- a layer can be formed. Therefore, this can be suitably used as a pressure-sensitive adhesive composition for polarizing plates.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Polarising Elements (AREA)
- Adhesive Tapes (AREA)
Abstract
Description
次の成分(A)および(B)
(A)少なくともカルボキシル基含有モノマー1~10質量%を共重合し てなる重量平均分子量が30万~150万である(メタ)アクリル系 ポリマー 100質量部
(B)イソシアヌレート構造を有するトリレンジイソシアネート系化合物
4~20質量部
を含有することを特徴とする偏光板用粘着剤組成物である。
1/Tg=Wa/Tga+Wb/Tgb+・・・
Tg:共重合体のガラス転移温度
Tga,Tgb,・・:単量体a,単量体b,・・・のホモポリマーのガ ラス転移温度
Wa,Wb,・・・・:単量体a,単量体b,・・・の重量分率
すなわち、粘着剤にイソシアネート系化合物を過剰量添加すると、イソシアネート系化合物由来のポリ尿素が生成すると言われている。このポリ尿素が粘着剤の主ポリマーとからみ合って物理的結合を生じ、一般の粘着剤と同様の編み目構造を持つが、イソシアヌレート構造を有するトリレンジイソシアネート系化合物の場合にも、同様の絡み合いによる網目構造を持つと考えられる。イソシアヌレート構造を有するトリレンジイソシアネート系化合物由来のポリ尿素によって高弾性となり、併せて複屈折も制御できるため、光漏れ防止性が良好となり、さらに、イソシアヌレート構造を有するトリレンジイソシアネート系化合物は、他のイソシアネート系化合物と比較して反応性が高く、架橋反応やポリ尿素の生成反応が早いことから、熟成期間を大幅に短縮できるものと考えられる。
アクリル系ポリマーの製造:
撹拌機、窒素ガス導入管、温度計および還流冷却管を備えたフラスコに、ブチルアクリレート97質量部、アクリル酸3質量部、酢酸エチル100質量部、ノルマルドデシルメルカプタン(NDM)0.04質量部を仕込みフラスコ内に窒素ガスを導入しながらフラスコの内容物を60℃に加熱した。次いで、十分に窒素ガス置換した重合開始剤アゾビスイソブチロニトリル(AIBN)0.1質量部を攪拌下にフラスコ内に添加した。フラスコ内の内容物の温度が60℃に維持できるように、加熱及び冷却を10時間行い最後に酢酸エチル100部を添加してアクリル系ポリマーA1溶液を得た。このアクリル系ポリマーA1について、重量平均分子量(Mw)、数平均分子量(Mn)を下記GPC測定条件に従って測定し、分散度(Mw/Mn)を求めた。また、不揮発分(nV)および粘度についても下記方法により測定した。測定結果をモノマー組成と併せて表1に示す。
測定装置:HLC-8120GPC(東ソー社製)
GPCカラム構成:以下の5連カラム(すべて東ソー社製)
(1)TSK-GEL HXL-H (ガードカラム)
(2)TSK-GEL G7000HXL
(3)TSK-GEL GMHXL
(4)TSK-GEL GMHXL
(5)TSK-GEL G2500HXL
サンプル濃度:1.0mg/cm3となるように、テトラヒドロフランで希釈
移動相溶媒:テトラヒドロフラン
流量: 1ml/min
カラム温度:40℃
精秤したブリキシャーレ(n1)にアクリル系共重合体溶液を1g程度入れ、合計重量(n2)を精秤した後、105℃で3時間加熱した。その後、このブリキシャーレを室温のデシケータ内に1時間静置し、次いで再度精秤し加熱後の合計重量(n3)を測定した。得られた重量測定値(n1~n3)を用いて下記式から不揮発分を算出した。
不揮発分(%)=100×[加熱後重量(n3-n1)/加熱前重量(n2-n1)]
B型粘度計を使用して、室温にて測定した。
表1に示すモノマー組成に代えた以外は製造例1と同様にしてアクリル系ポリマーA2~A6溶液を得た。このポリマーのMw、Mn、不揮発分、粘度を製造例1と同様にして測定した。結果を表1に示す。
表1に示すモノマー組成に代えた以外は製造例1と同様にしてアクリル系ポリマーB1~B4溶液を得た。このポリマーのMw、Mn、不揮発分、粘度を製造例1と同様にして測定した。結果を表1に示す。
粘着剤層を有する偏光板の作製:
(粘着剤組成物の調製)
製造例1により得られたアクリル系ポリマーA1溶液のアクリル系ポリマーA1(固形分)100質量部に対して、トリレンジイソシアネート(TDI)系のイソシアヌレート変性体であるコロネート342(日本ポリウレタン社製)5質量部、シランカップリング剤としてKBM-403(信越化学工業株式会社製)0.2質量部を添加し、これらを充分混合して粘着剤組成物を得た。
泡抜け後、ドクターブレードを用い剥離処理されたポリエステルフィルムに塗工し、すぐに90℃で3分間乾燥した。乾燥後、偏光板に張り合わせ、室温23℃、湿度50%の条件で静置して熟成させて粘着剤層を有する偏光板を得た。熟成期間は、1日、3日、7日とした。
アクリル系ポリマーおよび架橋剤を下記表2のように代えた以外は実施例1と同様にして粘着剤組成物を得た。また、得られた粘着剤組成物を用い、実施例1と同様にして粘着剤層を有する偏光板を作製した。
アクリル系ポリマーおよび架橋剤を下記表3のように代えた以外は実施例1と同様にして粘着剤組成物を得た。また、得られた粘着剤組成物を用い、実施例1と同様にして粘着剤層を有する偏光板を作製した。
実施例1~12および比較例1~11で得た偏光板のうち、熟成期間が1日と7日のものについて、耐久性、光漏れ防止性を以下の方法により評価した。これらの結果を表2および3にまとめて示す。
粘着剤層を有する偏光板を、150mm×250mmの大きさに裁断し、ガラス板の片面にラミネーターロールを用いて貼着し、次いで、50℃、5気圧に調整されたオートクレーブに20分間保持して、試験板を作成した。同様の試験板を2枚作成し、温度60℃、湿度95%RHの条件下(耐湿熱性)及び温度85℃の条件下(耐熱性)で500時間放置し、以下の基準でハガレの発生等を目視で観察し評価した。
(基準)
○:発泡、ハガレ、きれつは見られない
△:発泡、ハガレ、きれつがやや見られる
×:発泡、ハガレ、きれつが全面に見られる
粘着剤層を有する偏光板2枚を、19インチワイドTNモニタ(型番:BenQ FP93VW)の表裏面に相互に直交ニコル位になるようにラミネーターロールを用いて貼着し、次いで、50℃、5気圧に調整されたオートクレーブに20分間保持して、試験板を作成した。作成した試験板を、70℃の条件下で500時間放置し、光漏れを目視で観察し、以下の基準で評価した。
(基準)
○:光漏れが見られない
△:光漏れが一部見られる
×:光漏れが全面に見られる
実施例1~12および比較例1~11で得られた熟成1、3、7日の粘着剤層を有する偏光板について、以下の方法により粘着力を評価した。また実施例1~12および比較例1~11で得られた粘着剤組成物により形成される粘着剤層について、以下の方法により熟成1、3、7日におけるゲル分率を評価した。これらの結果を表4に示す。
粘着剤層を有する偏光板を70mm×25mmの大きさに裁断し試験片を作成した。試験片からポリエステルフィルムを剥離し、ガラス板の片面にラミネーターロールを用いて貼着した後、50℃、5気圧に調整されたオートクレーブ中に20分間保持した。次いで23℃、50%RH環境下に1時間放置した後、90°方向に300mm/minの速度で引っ張り、剥離強度を測定した。
得られた粘着剤組成物を乾燥後の厚みが20μmになるように剥離処理したポリエステルの表面に塗布し、乾燥させた後、もう一方の面に剥離処理したポリエステルフィルムを張り合わせて、23℃、50%RHで1、3、7日間熟成させて、試験片を作製した。試験片から粘着剤約0.1gをサンプル瓶に採取し、酢酸エチル30ccを加えて24時間振とうした後、該サンプル瓶の内容物を200メッシュのステンレス製金綱でろ別し、金綱上の残留物を100℃で2時間乾燥させて、乾燥重量を測定し、次式より求めた。
ゲル分率(%)=(乾燥重量/採取した粘着剤重量)×100
Claims (8)
- 次の成分(A)および(B)
(A)少なくともカルボキシル基含有モノマー1~10質量%を共 重合してなる重量平均分子量が30万~150万である(メ タ)アクリル系ポリマー 100質量部
(B)イソシアヌレート構造を有するトリレンジイソシアネート系 化合物 4~20質量部
を含有することを特徴とする偏光板用粘着剤組成物。 - 成分(A)が、さらに水酸基含有(メタ)アクリル系モノマー0.05~1質量%を共重合して得られるものである請求項1記載の偏光板用粘着剤組成物。
- さらに成分(C)トリレンジイソシアネート系架橋剤(イソシアヌレート構造を有するものを除く)、エポキシ系架橋剤およびアジリジン系架橋剤よりなる群から選ばれる1種または2種以上の架橋剤を含有する請求項1記載の偏光板用粘着剤組成物。
- さらに成分(D)シランカップリング剤を含有する請求項1ないし3のいずれかの項記載の偏光板用粘着剤組成物。
- 支持体の少なくとも一方の面に請求項1記載の偏光板用粘着剤組成物から形成される粘着剤層を設けてなる偏光板用粘着シート。
- 偏光フィルムの少なくとも一方の面に請求項1記載の偏光板用粘着剤組成物から形成される粘着剤層を設けてなる偏光板。
- 次の成分(A)および(B)
(A)少なくともカルボキシル基含有モノマー1~10質量%を共 重合してなる重量平均分子量が30万~150万である(メ タ)アクリル系ポリマー 100質量部
(B)イソシアヌレート構造を有するトリレンジイソシアネート系 化合物 4~20質量部
を含有する粘着剤組成物から形成される粘着剤層を偏光フィルムの少なくとも一方の面に設けた偏光板を液晶セルの基板表面に設けることを特徴とする液晶素子の製造方法。 - 次の成分(A)および(B)
(A)少なくともカルボキシル基含有モノマー1~10質量%を共 重合してなる重量平均分子量が30万~150万である(メ タ)アクリル系ポリマー 100質量部
(B)イソシアヌレート構造を有するトリレンジイソシアネート系 化合物 4~20質量部
を含有する粘着剤組成物から形成される粘着剤層を偏光フィルムの少なくとも一方の面に設けた偏光板を液晶セルの基板表面に設けることを特徴とする液晶表示装置の光漏れ低減方法。
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201080046723.5A CN102686689B (zh) | 2009-11-17 | 2010-11-15 | 偏光板用粘合剂组合物以及利用了该组合物的偏光板 |
JP2011541907A JP5764496B2 (ja) | 2009-11-17 | 2010-11-15 | 偏光板用粘着剤組成物およびこれを利用した偏光板 |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2009261506 | 2009-11-17 | ||
JP2009-261506 | 2009-11-17 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2011062127A1 true WO2011062127A1 (ja) | 2011-05-26 |
Family
ID=44059605
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2010/070260 WO2011062127A1 (ja) | 2009-11-17 | 2010-11-15 | 偏光板用粘着剤組成物およびこれを利用した偏光板 |
Country Status (5)
Country | Link |
---|---|
JP (1) | JP5764496B2 (ja) |
KR (1) | KR101587804B1 (ja) |
CN (1) | CN102686689B (ja) |
TW (1) | TWI486417B (ja) |
WO (1) | WO2011062127A1 (ja) |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2013001733A (ja) * | 2011-06-13 | 2013-01-07 | Nippon Carbide Ind Co Inc | 粘着剤組成物、それを用いた光学フィルム、および液晶表示装置 |
JP2013194151A (ja) * | 2012-03-21 | 2013-09-30 | Sumitomo Chemical Co Ltd | 粘着剤シート、粘着剤付き光学フィルム及び光学積層体 |
JP2013194152A (ja) * | 2012-03-21 | 2013-09-30 | Sumitomo Chemical Co Ltd | 粘着剤シート、粘着剤付き光学フィルム及び光学積層体 |
JP2014084386A (ja) * | 2012-10-23 | 2014-05-12 | Dainippon Printing Co Ltd | 粘着剤組成物、粘着シート及び画像表示装置 |
JP2014118485A (ja) * | 2012-12-17 | 2014-06-30 | Fujimori Kogyo Co Ltd | 粘着剤層、及び粘着フィルム |
WO2016072197A1 (ja) * | 2014-11-04 | 2016-05-12 | 綜研化学株式会社 | 偏光板用粘着剤組成物および粘着剤層付き偏光板 |
JP2016196647A (ja) * | 2016-06-08 | 2016-11-24 | 住友化学株式会社 | 粘着剤シート、粘着剤付き光学フィルム及び光学積層体 |
JP2016216722A (ja) * | 2016-06-08 | 2016-12-22 | 住友化学株式会社 | 粘着剤シート、粘着剤付き光学フィルム及び光学積層体 |
JP2017193608A (ja) * | 2016-04-19 | 2017-10-26 | 東洋インキScホールディングス株式会社 | 粘着剤および粘着シート |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR102294142B1 (ko) * | 2018-06-22 | 2021-08-26 | 산진 옵토일렉트로닉스 (쑤저우) 컴퍼니 리미티드 | 편광판 점착제 유출 여부 또는 유출 정도의 정량화 방법 |
CN111548761B (zh) * | 2019-02-08 | 2023-08-18 | 日本电石工业株式会社 | 偏振片用粘合剂组合物、带有粘合剂层的偏振片和车载显示装置 |
CN113755101A (zh) * | 2021-09-07 | 2021-12-07 | 常州都铂高分子有限公司 | 一种具有良好再剥离性的胶水组合物 |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2007119667A (ja) * | 2005-10-31 | 2007-05-17 | Sumitomo Chemical Co Ltd | 粘着剤 |
Family Cites Families (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH04136524A (ja) | 1990-09-27 | 1992-05-11 | Nissan Motor Co Ltd | 湿式摩擦係合板 |
JP3830375B2 (ja) * | 2001-11-07 | 2006-10-04 | リンテック株式会社 | 粘着シート用プライマー、粘着シート貼付製品及びその製造方法 |
JP2003154797A (ja) * | 2001-11-26 | 2003-05-27 | Toppan Printing Co Ltd | 転写シート |
JP4134350B2 (ja) * | 2002-08-29 | 2008-08-20 | 綜研化学株式会社 | 光学部材用粘着剤及び該粘着剤を用いた光学部材 |
JP4623485B2 (ja) | 2004-03-02 | 2011-02-02 | サイデン化学株式会社 | 粘着剤組成物及び表面保護フィルム |
JP4976075B2 (ja) * | 2005-12-26 | 2012-07-18 | リンテック株式会社 | 偏光板用粘着剤、粘着剤付き偏光板及びその製造方法 |
JP2008144126A (ja) | 2006-11-17 | 2008-06-26 | Fujifilm Corp | アクリレート系粘着剤ならびにそれを用いた偏光板および液晶表示装置 |
JP5717940B2 (ja) | 2006-12-25 | 2015-05-13 | 日東電工株式会社 | 混合物の硬化促進方法および粘着剤組成物の硬化促進方法 |
JP2009132751A (ja) * | 2007-11-28 | 2009-06-18 | Cheil Industries Inc | 粘着剤組成物及び光学部材 |
JP2009132752A (ja) * | 2007-11-28 | 2009-06-18 | Cheil Industries Inc | 粘着剤組成物及び光学部材 |
JP4963485B2 (ja) * | 2008-04-07 | 2012-06-27 | 綜研化学株式会社 | 偏光板用粘着剤組成物およびその製造方法 |
JP5304339B2 (ja) * | 2009-03-11 | 2013-10-02 | 東洋インキScホールディングス株式会社 | 粘着剤組成物及びそれを用いてなる粘着積層体 |
JP5526645B2 (ja) * | 2009-08-07 | 2014-06-18 | 東洋インキScホールディングス株式会社 | 光学用粘着剤および該光学用粘着剤を用いた光学用粘着シート |
-
2010
- 2010-11-12 TW TW099139043A patent/TWI486417B/zh not_active IP Right Cessation
- 2010-11-15 CN CN201080046723.5A patent/CN102686689B/zh not_active Expired - Fee Related
- 2010-11-15 KR KR1020127003032A patent/KR101587804B1/ko active IP Right Grant
- 2010-11-15 WO PCT/JP2010/070260 patent/WO2011062127A1/ja active Application Filing
- 2010-11-15 JP JP2011541907A patent/JP5764496B2/ja not_active Expired - Fee Related
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2007119667A (ja) * | 2005-10-31 | 2007-05-17 | Sumitomo Chemical Co Ltd | 粘着剤 |
Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2013001733A (ja) * | 2011-06-13 | 2013-01-07 | Nippon Carbide Ind Co Inc | 粘着剤組成物、それを用いた光学フィルム、および液晶表示装置 |
JP2013194151A (ja) * | 2012-03-21 | 2013-09-30 | Sumitomo Chemical Co Ltd | 粘着剤シート、粘着剤付き光学フィルム及び光学積層体 |
JP2013194152A (ja) * | 2012-03-21 | 2013-09-30 | Sumitomo Chemical Co Ltd | 粘着剤シート、粘着剤付き光学フィルム及び光学積層体 |
JP2014084386A (ja) * | 2012-10-23 | 2014-05-12 | Dainippon Printing Co Ltd | 粘着剤組成物、粘着シート及び画像表示装置 |
JP2014118485A (ja) * | 2012-12-17 | 2014-06-30 | Fujimori Kogyo Co Ltd | 粘着剤層、及び粘着フィルム |
WO2016072197A1 (ja) * | 2014-11-04 | 2016-05-12 | 綜研化学株式会社 | 偏光板用粘着剤組成物および粘着剤層付き偏光板 |
KR20170078631A (ko) * | 2014-11-04 | 2017-07-07 | 소켄 케미칼 앤드 엔지니어링 캄파니, 리미티드 | 편광판용 점착제 조성물 및 점착제층 부착 편광판 |
JPWO2016072197A1 (ja) * | 2014-11-04 | 2017-08-17 | 綜研化学株式会社 | 偏光板用粘着剤組成物および粘着剤層付き偏光板 |
KR102135645B1 (ko) * | 2014-11-04 | 2020-07-20 | 소켄 케미칼 앤드 엔지니어링 캄파니, 리미티드 | 편광판용 점착제 조성물 및 점착제층 부착 편광판 |
JP2017193608A (ja) * | 2016-04-19 | 2017-10-26 | 東洋インキScホールディングス株式会社 | 粘着剤および粘着シート |
JP2016196647A (ja) * | 2016-06-08 | 2016-11-24 | 住友化学株式会社 | 粘着剤シート、粘着剤付き光学フィルム及び光学積層体 |
JP2016216722A (ja) * | 2016-06-08 | 2016-12-22 | 住友化学株式会社 | 粘着剤シート、粘着剤付き光学フィルム及び光学積層体 |
Also Published As
Publication number | Publication date |
---|---|
KR101587804B1 (ko) | 2016-01-22 |
CN102686689A (zh) | 2012-09-19 |
CN102686689B (zh) | 2015-12-16 |
KR20120115203A (ko) | 2012-10-17 |
TW201132723A (en) | 2011-10-01 |
JPWO2011062127A1 (ja) | 2013-04-04 |
TWI486417B (zh) | 2015-06-01 |
JP5764496B2 (ja) | 2015-08-19 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP5764496B2 (ja) | 偏光板用粘着剤組成物およびこれを利用した偏光板 | |
JP5505766B2 (ja) | 偏光板用粘着剤組成物およびこれを利用した偏光板 | |
JP5435433B2 (ja) | 偏光板用粘着剤組成物およびこれを利用した偏光板 | |
WO2010024103A1 (ja) | 粘着剤組成物、粘着剤、及び光学フィルム | |
JP3997270B2 (ja) | 光学フィルム用粘着剤組成物および粘着シート、ならびにこれを用いた光学部材 | |
KR101796142B1 (ko) | 점착성 조성물, 점착제 및 점착시트 | |
JP3997271B2 (ja) | 光学フィルム用粘着剤組成物および粘着シート、ならびにこれを用いた光学部材 | |
TWI417358B (zh) | 光學薄膜用黏著劑及黏著加工光學薄膜 | |
JP5923231B2 (ja) | 粘着剤組成物、光学フィルム、及び粘着剤組成物の製造方法 | |
TWI666282B (zh) | 黏著劑組成物、黏著劑層、黏著片及觸控板用積層體 | |
JP2003049141A (ja) | 偏光板用粘着剤組成物 | |
WO2007058277A1 (ja) | 光学フィルム用粘着剤組成物および粘着シート、ならびにこれを用いた光学部材 | |
JP5562173B2 (ja) | 粘着性組成物、粘着剤および粘着シート | |
JP5912370B2 (ja) | 粘着剤組成物及びこれを用いた光学部材 | |
WO2012157630A1 (ja) | 光学部材用粘着剤組成物およびその加工製品 | |
JP2009191149A (ja) | 偏光板用粘着剤組成物およびこれを利用した偏光板 | |
KR20110131173A (ko) | 아크릴계 점착제 및 이것을 이용한 편광 필름용 점착 시트 및 점착형 편광 필름 | |
JP5544858B2 (ja) | 偏光板用粘着剤組成物 | |
KR20150016561A (ko) | 편광판용 점착제 조성물, 점착제가 부착된 편광판 및 표시 장치 | |
JP5611880B2 (ja) | 粘着剤および粘着シート | |
JP5638439B2 (ja) | 粘着剤および粘着シート | |
JP5602670B2 (ja) | 粘着剤および粘着シート | |
CN105524577A (zh) | 粘合剂组合物和粘合片 | |
JP2014221898A (ja) | 粘着性組成物、粘着剤および粘着シート | |
JP2012184432A (ja) | 光学用粘着剤組成物および粘着シート |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
WWE | Wipo information: entry into national phase |
Ref document number: 201080046723.5 Country of ref document: CN |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 10831521 Country of ref document: EP Kind code of ref document: A1 |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2011541907 Country of ref document: JP |
|
ENP | Entry into the national phase |
Ref document number: 20127003032 Country of ref document: KR Kind code of ref document: A |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
122 | Ep: pct application non-entry in european phase |
Ref document number: 10831521 Country of ref document: EP Kind code of ref document: A1 |