WO2013183563A1 - Composition adhésive pour des plaques de polarisation, plaque de polarisation ayant un adhésif et dispositif d'affichage - Google Patents

Composition adhésive pour des plaques de polarisation, plaque de polarisation ayant un adhésif et dispositif d'affichage Download PDF

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Publication number
WO2013183563A1
WO2013183563A1 PCT/JP2013/065228 JP2013065228W WO2013183563A1 WO 2013183563 A1 WO2013183563 A1 WO 2013183563A1 JP 2013065228 W JP2013065228 W JP 2013065228W WO 2013183563 A1 WO2013183563 A1 WO 2013183563A1
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Prior art keywords
acrylic copolymer
meth
acrylate
unit derived
structural unit
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PCT/JP2013/065228
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English (en)
Japanese (ja)
Inventor
太郎 川口
宏人 中野
直人 安田
雅樹 西田
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日本カーバイド工業株式会社
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Application filed by 日本カーバイド工業株式会社 filed Critical 日本カーバイド工業株式会社
Priority to CN201380029297.8A priority Critical patent/CN104379694B/zh
Priority to KR1020147034956A priority patent/KR102090220B1/ko
Priority to JP2014519968A priority patent/JP6002220B2/ja
Publication of WO2013183563A1 publication Critical patent/WO2013183563A1/fr

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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
    • 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
    • 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
    • C09J133/062—Copolymers with monomers not covered by C09J133/06
    • C09J133/066—Copolymers with monomers not covered by C09J133/06 containing -OH 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
    • C08G18/28—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
    • C08G18/622—Polymers of esters of alpha-beta ethylenically unsaturated carboxylic acids
    • C08G18/6225—Polymers of esters of acrylic or methacrylic acid
    • C08G18/6229—Polymers of hydroxy groups containing esters of acrylic or methacrylic acid with aliphatic polyalcohols
    • 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
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L33/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
    • C08L33/04—Homopolymers or copolymers of esters
    • C08L33/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, which oxygen atoms are present only as part of the carboxyl radical
    • C08L33/062—Copolymers with monomers not covered by C08L33/06
    • C08L33/066—Copolymers with monomers not covered by C08L33/06 containing -OH groups
    • 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
    • C09J133/02—Homopolymers or copolymers of acids; Metal or ammonium salts thereof
    • 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
    • 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
    • G02F—OPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
    • G02F1/00—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
    • G02F1/01—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour 
    • G02F1/13—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour  based on liquid crystals, e.g. single liquid crystal display cells
    • G02F1/133—Constructional arrangements; Operation of liquid crystal cells; Circuit arrangements
    • G02F1/1333—Constructional arrangements; Manufacturing methods
    • G02F1/1334—Constructional arrangements; Manufacturing methods based on polymer dispersed liquid crystals, e.g. microencapsulated liquid crystals

Definitions

  • the present invention relates to a pressure-sensitive adhesive composition for a polarizing plate, a polarizing plate with a pressure-sensitive adhesive, and a display device.
  • a liquid crystal display device for displaying an image such as a liquid crystal display device or organic electroluminescence
  • a liquid crystal display device generally includes a liquid crystal cell in which a liquid crystal component oriented in a predetermined direction is sandwiched between two supporting substrates such as glass, and an optical film such as a polarizing plate, a retardation film, and a brightness enhancement film. Are bonded together.
  • An adhesive is used when laminating optical films or sticking an optical film to a liquid crystal cell.
  • Liquid crystal display devices are widely used as display devices for personal computers, televisions, car navigation systems, etc.
  • various liquid crystal display devices such as harsh environmental conditions with a high amount of high temperature and high humidity and dry environmental conditions with low humidity. Used under environmental conditions. Therefore, even when used for a long period of time, the bonded part (that is, the interface between the pressure-sensitive adhesive layer and the liquid crystal cell or the polarizing film) peeled off or the pressure-sensitive adhesive layer is broken. It is required that the adhesive layer has a high durability performance such that bubbles are not easily generated.
  • the polarizing plate has a polarizing film (polarizer) using PVA or the like.
  • polarizing film polarizer
  • a stretched film for this polarizing film, for example, when exposed to a severe environment such as high temperature and high humidity, a dimensional change accompanying shrinkage or expansion is likely to occur, and stress is generated in the polarizing plate.
  • the stress accompanying the dimensional change is not relaxed by the adhesive disposed between the polarizing plate and the liquid crystal cell, the residual stress is generated unevenly in the polarizing plate.
  • a phase shift occurs between the two polarizing plates arranged so that the extending axes of the polarizing film intersect each other between the front surface and the back surface of the display panel. For this reason, light leaks from the four surroundings of the display portion of the liquid crystal display device and becomes white, so-called “white spots” occur.
  • a soft soft type adhesive is used for a small display panel, and a relatively hard type adhesive is used for a large display panel.
  • this hard type adhesive is applied to a small display panel, the stress accompanying shrinkage or the like tends to concentrate on the edge, and the above-described white spots tend to appear remarkably around the panel.
  • a large-sized pressure-sensitive adhesive is produced for a large display panel application, the end portion of the original fabric cannot be used effectively, which is a cause of a decrease in yield.
  • the soft type adhesive is soft, it tends to adhere to the processing blade and tends to be inferior in punching suitability.
  • a pressure-sensitive adhesive that relaxes stress by adding a low molecular weight polymer to the pressure-sensitive adhesive composition.
  • a pressure-sensitive adhesive composition for a polarizing plate comprising a high molecular weight acrylic copolymer, a low molecular weight acrylic copolymer having a weight average molecular weight of 30,000 or less, and a polyfunctional compound is disclosed.
  • a pressure-sensitive adhesive composition for a polarizing plate containing an isocyanate compound is disclosed, which has durability under high temperature and high humidity and suppresses white spots (for example, see Patent Document 2).
  • the pressure-sensitive adhesive has been conventionally adjusted according to the application and size. On the other hand, it can be applied to both large display panel applications and small display panel applications. Regardless of size, the occurrence of white spots is prevented and the adhesive has excellent durability and workability. The reality is that it has not yet been proposed.
  • the present invention has been made in view of the above. Under the circumstances described above, a pressure-sensitive adhesive composition for a polarizing plate and a pressure-sensitive adhesive with a pressure-sensitive adhesive that has high durability that hardly causes foaming or peeling, and that suppresses occurrence of color unevenness (particularly white spots) regardless of size. Is needed. Further, there is a need for a display device that displays an image with little color unevenness.
  • the present invention has been achieved based on the following findings. That is, When two or more types of resins having different weight average molecular weights are blended and used, a resin having a low molecular weight out of two or more types of resins does not have a polar group such as a hydroxyl group but has a molecular weight higher than that of the resin having a polar group.
  • a crosslinking agent When the reactivity with a crosslinking agent is small compared to a resin with a large size, the durability tends to decrease due to a decrease in molecular weight, but the reaction with an isocyanate-based crosslinking agent focuses on the glass transition temperature of the resin. It is the knowledge that the durability of the pressure-sensitive adhesive and the prevention of color unevenness can be achieved by adjusting the copolymerization component.
  • 1st this invention contains the structural unit derived from the monomer which has a carboxy group and the structural unit derived from the alkyl (meth) acrylate, and the weight average molecular weight is 300,000 or more and 700,000 or less
  • the amount of the acrylic copolymer B that is from 1,000,000 to 2,000,000 and the total amount of the acrylic copolymer A and the acrylic copolymer B of 100 parts by mass is 20 parts by mass or less.
  • an acrylic crosslinking agent having a glass transition temperature (TgA) of the acrylic copolymer A is a glass transition of the acrylic copolymer B. It is degrees (TgB) or a polarizing plate for a pressure-sensitive adhesive composition.
  • 2nd this invention is a polarizing plate with an adhesive which has a polarizer and the adhesive layer formed on the said polarizer by provision of the adhesive composition for polarizing plates of said 1st invention.
  • a pressure-sensitive adhesive composition for a polarizing plate and a polarizing plate with a pressure-sensitive adhesive which have high durability in which foaming, peeling, etc. are unlikely to occur, and generation of color unevenness (particularly white spots) is suppressed regardless of size.
  • ADVANTAGE OF THE INVENTION According to this invention, the display apparatus with which an image with little color unevenness is displayed is provided.
  • the pressure-sensitive adhesive composition for polarizing plates of the present invention includes a structural unit derived from an alkyl (meth) acrylate and a structural unit derived from a monomer having a carboxy group, and has a weight average molecular weight of 300,000 or more and 700,000.
  • Acrylic copolymer A and a structural unit derived from an alkyl (meth) acrylate, a structural unit derived from a monomer having a carboxy group, and a structural unit derived from a monomer having a hydroxyl group The acrylic copolymer B having a weight average molecular weight of 1,000,000 or more and 2,000,000 or less and an isocyanate crosslinking agent are used.
  • the pressure-sensitive adhesive composition for a polarizing plate of the present invention has an isocyanate cross-linking agent content of 20 parts by mass or less with respect to a total amount of 100 parts by mass of the acrylic copolymer A and the acrylic copolymer B.
  • the glass transition temperature (TgA) of the acrylic copolymer A and the glass transition temperature (TgB) of the acrylic copolymer B satisfy the relationship of TgA ⁇ TgB.
  • the pressure-sensitive adhesive composition for a polarizing plate of the present invention may further include a crosslinking agent, a silane coupling agent, other additives, etc. as necessary. Other components may be included.
  • a relatively high-polarity isocyanate cross-linking agent is used in a predetermined ratio as a cross-linking agent, and at least a high molecular weight side acrylic copolymer B is provided with a hydroxyl group as a polar group so that a low molecular weight side acrylic copolymer A is present.
  • the glass transition temperature (TgA) is set to be equal to or higher than the glass transition temperature (TgB) of the acrylic copolymer B. Thereby, reaction with the isocyanate type crosslinking agent of the acrylic copolymer A of the low molecular weight side is promoted. By reducing the molecular weight of the acrylic copolymer, stress relaxation is provided, and embrittlement associated with the lower molecular weight is prevented, and color unevenness (especially white spots) in the pressure-sensitive adhesive regardless of the size. Both prevention of occurrence and improvement of durability are achieved.
  • the pressure-sensitive adhesive composition for polarizing plates of the present invention is excellent in durability and color unevenness (particularly white spotting) prevention, it can be suitably used for large display panels of 19 inches or more (that is, large display devices). At the same time, it can be suitably used for a small display panel (that is, a small display device) of less than 19 inches (or even less than 10 inches).
  • the pressure-sensitive adhesive composition for polarizing plates of the present invention can produce a large-sized display panel-use pressure-sensitive adhesive, and can produce a small-sized display panel-use pressure-sensitive adhesive from the edge of the original fabric, so the yield is high. improves. Therefore, it becomes possible to manufacture large and small pressure-sensitive adhesives according to the required amount, and there is an advantage that the necessity of inventory and storage is eliminated.
  • (meth) acryl means acryl or methacryl
  • (meth) acrylate means acrylate or methacrylate
  • the pressure-sensitive adhesive composition for polarizing plates of the present invention includes a structural unit derived from an alkyl (meth) acrylate and a structural unit derived from a monomer having a carboxy group, and has a weight average molecular weight of 300,000 or more and 700,000. It contains at least one of the following acrylic copolymers A.
  • This acrylic copolymer A is a copolymer obtained by copolymerizing at least an alkyl (meth) acrylate and a monomer having a carboxy group, and further derived from the monomer by copolymerization with another monomer. It may further have a structural unit.
  • alkyl (meth) acrylate constituting the acrylic copolymer A examples include methyl (meth) acrylate, ethyl (meth) acrylate, n-butyl (meth) acrylate, i-butyl (meth) acrylate, and t-butyl.
  • alkyl (meth) acrylates having 1 to 4 carbon atoms are preferable, alkyl acrylates having 1 to 4 carbon atoms are preferable, and n-butyl acrylate is particularly preferable in terms of easily adjusting the cohesive force and adhesive force of the pressure-sensitive adhesive. .
  • the ratio of the structural unit derived from the alkyl (meth) acrylate in the acrylic copolymer A is preferably 65.0 to 99.5% by mass, more preferably 65.0 to 94.5% by mass, and 75.%. 0 to 90.0% by mass is particularly preferable.
  • Alkyl (meth) acrylate is contained as a main component constituting the copolymer, and when the content ratio is within the above range, it can be adjusted to an optimal elastic modulus, in terms of ensuring durability and tackiness. It is advantageous.
  • the acrylic copolymer A according to the present invention further includes the alkyl (meth) acrylate (preferably a monomer different from the alkyl (meth) acrylate).
  • the alkyl (meth) acrylate preferably a monomer different from the alkyl (meth) acrylate.
  • the glass transition temperature is increased, that is, the polarity of the resin is increased, the reactivity with the isocyanate-based crosslinking agent is increased, and the durability can be further improved.
  • methyl acrylate, t-butyl acrylate, phenoxyethyl acrylate, and n-butyl methacrylate are preferable as monomers capable of forming a homopolymer having a glass transition temperature having an absolute value of the difference in the above range.
  • Particularly preferred acrylic copolymer A is an embodiment in which n-butyl acrylate is copolymerized with methyl acrylate and / or t-butyl acrylate.
  • the monomer (preferably methyl acrylate or t-butyl acrylate) other than the above-mentioned monomer (preferably methyl acrylate or t-butyl acrylate) is included in addition to the alkyl (meth) acrylate contained as the main component.
  • the ratio in the copolymer A is preferably 5 to 30% by mass, more preferably 5 to 20% by mass. When the content ratio is within the above range, it is advantageous in that the reactivity with the isocyanate-based crosslinking agent is enhanced.
  • a (meth) acrylic monomer having a carboxy group is preferable.
  • the monomer having a carboxy group include acrylic acid, methacrylic acid, and ⁇ -carboxy-polycaprolactone mono (meth) acrylate.
  • acrylic acid is preferable because it has high reactivity with other monomers during the copolymerization reaction and can reduce unreacted monomers.
  • the ratio of the structural unit derived from the monomer having a carboxy group in the acrylic copolymer A is preferably 0.5 to 5% by mass, more preferably 0.5 to 3% by mass.
  • the content ratio of the monomer having a carboxy group is within the above range, it is advantageous from the viewpoint of ensuring pot life and appropriately adjusting the degree of cross-linking of the resin.
  • the weight average molecular weight of the acrylic copolymer A is 300,000 or more and 700,000 or less.
  • the weight average molecular weight being within the above range indicates that the acrylic copolymer A is a low molecular weight resin among a plurality of resins contained in the pressure-sensitive adhesive composition for polarizing plates. Further, if the weight average molecular weight of the acrylic copolymer A becomes too small, less than 300,000, peeling or the like is likely to occur, and durability (particularly durability when applied to a large size (for example, 19 inches or more)). Decreases.
  • the weight average molecular weight of the acrylic copolymer A exceeds 700,000, the molecular size approaches that of the acrylic copolymer B, and the acrylic copolymer A is used in combination with the acrylic copolymer A. Stress relaxation is reduced, and color unevenness (particularly white spots) cannot be suppressed. This is particularly noticeable when applied to large size (for example, 19 inches or more) applications.
  • the glass transition temperature (TgA) of the acrylic copolymer A is preferably in the range of ⁇ 50 ° C. to ⁇ 30 ° C., more preferably in the range of ⁇ 48 ° C. to ⁇ 40 ° C.
  • TgA glass transition temperature
  • the glass transition temperature (TgA) is preferably in the range of ⁇ 50 ° C. to ⁇ 30 ° C., more preferably in the range of ⁇ 48 ° C. to ⁇ 40 ° C.
  • TgA is ⁇ 50 ° C. or higher, the elastic modulus can be adjusted, and the durability and whiteout property are excellent.
  • TgA is ⁇ 30 ° C. or lower, the tackiness and the bonding suitability are excellent without extremely impairing the viscosity.
  • the content of the acrylic copolymer A in the pressure-sensitive adhesive composition for polarizing plate can be appropriately selected within the range satisfying the content ratio A / B described later.
  • the range of 50 mass% or more and 74 mass% or less is preferable with respect to the minute, and the range of 54 mass% or more and 69 mass% or less is more preferable.
  • flexibility is imparted to the pressure-sensitive adhesive, and color unevenness (particularly white spots) is suppressed due to stress relaxation.
  • the pressure-sensitive adhesive composition for polarizing plates of the present invention comprises a structural unit derived from an alkyl (meth) acrylate, a structural unit derived from a monomer having a carboxy group, and a structural unit derived from a monomer having a hydroxyl group. And at least one acrylic copolymer B having a weight average molecular weight of 1,000,000 or more and 2,000,000 or less.
  • the acrylic copolymer B is a copolymer obtained by copolymerizing at least an alkyl (meth) acrylate, a monomer having a carboxy group, and a monomer having a hydroxyl group. It may be copolymerized to further have a structural unit derived from the monomer.
  • alkyl (meth) acrylate constituting the acrylic copolymer B examples include, for example, methyl (meth) acrylate, ethyl (meth) acrylate, n-butyl (meth) acrylate, i-butyl (meth) acrylate, and t-butyl.
  • alkyl (meth) acrylates having 1 to 8 carbon atoms are preferable, alkyl acrylates having 1 to 8 carbon atoms are preferable, and n-butyl acrylate, t -Butyl acrylate, methyl acrylate, 2-ethylhexyl acrylate are preferred.
  • the ratio of the structural unit derived from the alkyl (meth) acrylate in the acrylic copolymer B is preferably 93 to 99.4% by mass, and more preferably 96 to 99.4% by mass.
  • Alkyl (meth) acrylate is contained as a main component constituting the copolymer, and if the content ratio is within the above range, it can be adjusted to an optimal elastic modulus, which is advantageous in terms of durability and adhesive properties. is there.
  • a (meth) acrylic monomer having a carboxy group is preferable.
  • the monomer having a carboxy group include acrylic acid, methacrylic acid, and ⁇ -carboxy-polycaprolactone mono (meth) acrylate.
  • acrylic acid is preferable because it has high reactivity with other monomers during the copolymerization reaction and can reduce unreacted monomers.
  • the ratio of the structural unit derived from the monomer having a carboxy group in the acrylic copolymer B is preferably 0.5 to 5% by mass, and more preferably 0.5 to 3% by mass.
  • the content ratio of the monomer having a carboxy group is within the above range, it is advantageous in that the pot life property can be ensured and the resin crosslinking degree can be adjusted appropriately.
  • a (meth) acrylic monomer having a hydroxyl group is preferable, and a (meth) acrylic acid ester having a hydroxyl group is more preferable.
  • monomers having a hydroxyl group include 2-hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate, 3-hydroxypropyl (meth) acrylate, 4-hydroxybutyl (meth) acrylate, and 3-methyl.
  • hydroxyalkyl (meth) acrylates are preferred, and hydroxyalkyls having 1 to 4 carbon atoms in the alkyl moiety are preferred because of their high polymerization reactivity and excellent crosslinking reactivity when the resulting copolymer is included.
  • (Meth) acrylate is more preferable, and 2-hydroxyethyl acrylate, 2-hydroxypropyl acrylate, and 4-hydroxybutyl acrylate are more preferable.
  • the proportion of the structural unit derived from the monomer having a hydroxyl group in the acrylic copolymer B is preferably 0.1 to 2.0% by mass, more preferably 0.1 to 1.0% by mass.
  • the content ratio of the monomer having a hydroxyl group is within the above range, the reactivity with the isocyanate-based crosslinking agent can be ensured, which is advantageous for maintaining good durability.
  • the weight average molecular weight of the acrylic copolymer B is 1,000,000 or more and 2,000,000 or less.
  • a weight average molecular weight within the above range indicates that acrylic copolymer B is a high molecular weight resin among a plurality of resins contained in the pressure-sensitive adhesive composition for polarizing plates. Further, when the weight average molecular weight of the acrylic copolymer B is reduced to less than 1,000,000, peeling or the like easily occurs, and durability (particularly durability when applied to a large size (for example, 19 inches or more)). Decreases. When the weight average molecular weight of the acrylic copolymer B exceeds 2,000,000, the stress relaxation effect due to the combined use of the acrylic copolymer A decreases.
  • the glass transition temperature (TgB) of the acrylic copolymer B is preferably in the range of ⁇ 50 ° C. to ⁇ 40 ° C., and more preferably in the range of ⁇ 50 ° C. to ⁇ 45 ° C.
  • TgB is ⁇ 50 ° C. or higher, the elastic modulus can be adjusted, and the durability and whiteout property are excellent. Further, when TgB is ⁇ 40 ° C. or lower, the tackiness and the bonding suitability are excellent without extremely impairing the viscosity.
  • the content of the acrylic copolymer B in the pressure-sensitive adhesive composition for polarizing plates can be appropriately selected as long as the content ratio A / B described later is satisfied.
  • the range of 17 mass% or more and 37 mass% or less is preferable with respect to the minute, and the range of 21 mass% or more and 32 mass% or less is more preferable.
  • the content of the acrylic copolymer B is within the above range, the ratio of the high molecular weight component in the pressure-sensitive adhesive is maintained, and the durability is improved.
  • the monomer having an alkyl (meth) acrylate and a carboxy group constituting each of them is an acrylic copolymer A and an acrylic copolymer B. And may be different from each other or the same.
  • the glass transition temperature (TgA; ° C) of the acrylic copolymer A and the glass transition temperature (TgB; ° C) of the acrylic copolymer B satisfy the relationship of TgA ⁇ TgB. If TgA is less than TgB, the molecular weight is relatively small, and the reactivity with the isocyanate-based crosslinking agent is insufficient, so that failure such as foaming or peeling is likely to occur, resulting in poor durability.
  • the difference between TgA and TgB (TgA-TgB; ° C) is preferably in the range of 1 ° C to 5 ° C. A range of not less than 3 ° C and not more than 3 ° C is more preferable.
  • the glass transition temperature (Tg) of the acrylic copolymer is a molar average glass transition temperature determined by the following calculation.
  • m 1 , m 2 ,... and mn are the mole fractions of the respective components.
  • the “glass transition temperature (Tg) of the homopolymer” mentioned here includes L.P. E. The glass transition temperatures of the monomers described in Nielsen, Nojiharu Onoki, “Mechanical Properties of Polymers”, pp. 11-35, apply.
  • the ratio (MwA / MwB) of the weight average molecular weight (MwA) of the acrylic copolymer A to the weight average molecular weight (MwB) of the acrylic copolymer B is preferably 0.5 or less.
  • MwA / MwB is 0.5 or less, the effect of preventing color unevenness (particularly white spots) can be further enhanced.
  • MwA / MwB is more preferably 0.35 or less for the same reason as described above.
  • the content ratio (A / B) of the acrylic copolymer A to the acrylic copolymer B is preferably in the range of 60/40 to 80/20 on a mass basis.
  • the content ratio A / B is equal to or greater than the lower limit ratio, since the ratio of the acrylic copolymer A having a relatively small molecular weight is large, the effect of improving color unevenness (particularly white spots) due to stress relaxation is high, and the acrylic type Since the glass transition temperatures of the copolymers A and B satisfy the relationship of TgA ⁇ TgB, there is little concern about a decrease in durability due to a large proportion of the acrylic copolymer A.
  • the content ratio A / B is equal to or less than the upper limit ratio, the stress relaxation effect due to the lower molecular weight and the durability maintenance due to the relative amount of the acrylic copolymer B on the high molecular weight side being maintained. Can keep the balance.
  • the content ratio A / B is more preferably in the range of 65/35 to 75/25 for the same reason as described above.
  • Acrylic copolymer A is a structural unit derived from an alkyl (meth) acrylate having 1 to 4 carbon atoms, a structural unit derived from (meth) acrylic acid, and “the alkyl (meth) having 1 to 4 carbon atoms”.
  • Acrylic copolymer B is a structural unit derived from an alkyl (meth) acrylate having 1 to 8 carbon atoms, a structural unit derived from (meth) acrylic acid, a structural unit derived from hydroxyalkyl (meth) acrylate, (2)
  • the acrylic copolymer A is derived from a structural unit derived from n-butyl acrylate, a structural unit derived from a (meth) acrylic monomer having a carboxy group, and derived from methyl acrylate and / or t-butyl acrylate.
  • a structural unit, and Acrylic copolymer B is a structural unit derived from n-butyl acrylate, a structural unit derived from a (meth) acrylic monomer having a carboxy group, and a structural unit derived from hydroxyalkyl (meth) acrylate.
  • Acrylic copolymer A includes a structural unit derived from n-butyl acrylate, a structural unit derived from (meth) acrylic acid, and methyl acrylate and / or t-butyl acrylate
  • acrylic copolymer B includes a structural unit derived from n-butyl acrylate, a structural unit derived from (meth) acrylic acid, and a structural unit derived from hydroxyalkyl (meth) acrylate
  • the polymerization method of the acrylic copolymer in the present invention is not particularly limited, and methods such as solution polymerization, emulsion polymerization and suspension polymerization can be applied.
  • Solution polymerization is preferred because the treatment process is relatively simple and can be performed in a short time.
  • a predetermined organic solvent, a monomer, a polymerization initiator, and a chain transfer agent used as needed are generally charged in a polymerization tank, and stirred in a nitrogen stream or under reflux of the organic solvent. Heat the reaction for several hours.
  • the polymerization initiator is not particularly limited, and for example, an azo compound can be used.
  • the weight average molecular weight (Mw) of the acrylic copolymer can be adjusted to a desired molecular weight by adjusting the reaction temperature, time, amount of solvent, type and amount of catalyst.
  • the weight average molecular weight (Mw) of the acrylic copolymer is a value measured by the following method. That is, it is measured according to the following (1) to (3).
  • An acrylic copolymer solution is coated on a release sheet (release sheet) and dried at 100 ° C. for 2 minutes to obtain a film-like acrylic copolymer.
  • the film-like acrylic copolymer obtained in (1) is dissolved in tetrahydrofuran so that the solid content is 0.2% by mass.
  • the weight average molecular weight (Mw) of the (meth) acrylic copolymer is measured using gel permeation chromatography (GPC).
  • GPC HLC-8220 GPC [manufactured by Tosoh Corporation] ⁇ Column: TSK-GEL GMHXL (4 used) -Mobile phase solvent: Tetrahydrofuran-Standard sample: Standard polystyrene-Flow rate: 0.6 ml / min -Column temperature: 40 ° C
  • the pressure-sensitive adhesive composition for polarizing plates of the present invention contains at least one isocyanate-based crosslinking agent.
  • This cross-linking agent is a polar compound, and in the case of a composition containing such a cross-linking agent, the effects of the present invention (prevention of color unevenness (particularly white spots) and improvement in durability) are further exhibited.
  • a tolylene diisocyanate-based compound is preferably exemplified.
  • a tolylene diisocyanate compound derived from various isocyanates such as dimer or trimer of isocyanate or an adduct of isocyanate and trimethylolpropane polyol can be used.
  • tolylene diisocyanate compound a commercially available product may be used, and “Coronate L” (trade name) manufactured by Nippon Polyurethane Industry Co., Ltd. can be suitably used as an example of a commercially available product.
  • the content of the isocyanate-based crosslinking agent in the pressure-sensitive adhesive composition for polarizing plate is set to a range of 20 parts by mass or less with respect to 100 parts by mass of the total amount of the acrylic copolymer.
  • the content of the isocyanate cross-linking agent exceeds 20 parts by mass, the cohesive force becomes excessive, and when exposed to high temperature and high humidity, the polarizing plate (particularly cellulose triacetate (TAC), which is a protective sheet thereof) The adhesion between the two tends to deteriorate, and the occurrence of peeling cannot be suppressed.
  • TAC cellulose triacetate
  • an isocyanate type crosslinking agent As content of an isocyanate type crosslinking agent, the range of 8 mass parts or more and 20 mass parts or less is preferable, and the range of 10 mass parts or more and 15 mass parts or less is more preferable.
  • content of the isocyanate-based crosslinking agent is 8 parts by mass or more, good cohesive force is exhibited to suppress the shrinkage stress of the polarizing plate after the pressure-sensitive adhesive layer is adhered, and the occurrence of white spots is more effective. To be suppressed.
  • the pressure-sensitive adhesive composition for polarizing plates of the present invention preferably contains an epoxy crosslinking agent together with the isocyanate crosslinking agent.
  • the polarizing plate pressure-sensitive adhesive composition contains an epoxy-based crosslinking agent, the cohesive force can be easily adjusted, and abnormal appearance can be suppressed even when exposed to high temperatures and high humidity.
  • epoxy-based crosslinking agent examples include 1,3-bis (N, N-glycidylaminomethyl) cyclohexane, N, N, N ′, N′-tetraglycidyl-m-xylylenediamine and the like.
  • epoxy-based crosslinking agent commercially available products may be used.
  • commercially available products “TETRAD-X”, “TETRAD-C” (trade name) manufactured by Mitsubishi Gas Chemical Co., Ltd. It can be preferably used.
  • content in the adhesive composition for polarizing plates of an epoxy type crosslinking agent 0.001 mass% or more and 0.1 mass% with respect to the total amount of acrylic copolymer A and acrylic copolymer B
  • the following ranges are preferred.
  • the content of the epoxy crosslinking agent is within the above range, it is advantageous in that the cohesive force of the pressure-sensitive adhesive layer can be adjusted, and the occurrence of peeling due to durability (moisture and heat resistance) can be suppressed.
  • the adhesive composition for polarizing plates of this invention contains a silane coupling agent.
  • the pressure-sensitive adhesive composition for polarizing plate contains a silane coupling agent, the pressure-sensitive adhesive layer and the polarizing plate or liquid crystal even when a display device (for example, a liquid crystal display device) incorporating the polarizing plate is exposed to a high temperature and high humidity environment. Peeling hardly occurs between cells.
  • the pressure-sensitive adhesive composition for polarizing plates of the present invention is preferable in that it exhibits a good adhesive force on smooth glass.
  • silane coupling agent examples include polymerizable unsaturated group-containing silane compounds such as vinyltrimethoxysilane, vinyltriethoxysilane, and 3-methacryloxypropyltrimethoxysilane, 3-mercaptopropyltrimethoxysilane, and 3-mercapto.
  • Mercapto group-containing silane compounds such as propyltriethoxysilane and 3-mercaptopropyldimethoxymethylsilane, and epoxies such as 3-glycidoxypropyltrimethoxysilane and 2- (3,4-epoxycyclohexyl) ethyltrimethoxysilane Silane compounds having a structure, 3-aminopropyltrimethoxysilane, N- (2-aminoethyl) -3-aminopropyltrimethoxysilane, N- (2-aminoethyl) -3-aminopropylmethyldimethoxysilane, etc.
  • Amino group-containing silane compound, and tris - (3-trimethoxysilylpropyl) isocyanurate may be used alone or in combination of two or more.
  • silane coupling agent a commercially available product may be used, and “KBM-403” (trade name) manufactured by Shin-Etsu Chemical Co., Ltd. can be suitably used as an example of a commercially available product.
  • the adhesive composition for polarizing plates of a silane coupling agent 0.01 mass% or more with respect to 100 mass parts of total amounts of acrylic copolymer A and acrylic copolymer B 2.
  • a range of 0% by mass or less is preferred.
  • the adhesiveness of the pressure-sensitive adhesive layer can be further improved.
  • the pressure-sensitive adhesive composition for polarizing plates of the present invention may further contain various additives such as ultraviolet absorbers, solvents and the like.
  • the polarizing plate with the pressure-sensitive adhesive of the present invention comprises at least a polarizer and a pressure-sensitive adhesive layer formed on the polarizer by the application of the pressure-sensitive adhesive composition for a polarizing plate of the present invention described above. Yes.
  • a polyvinyl alcohol (PVA) film is generally used as the polarizer.
  • the polarizer can be used as a polarizing plate having, for example, a three-layer structure (for example, TAC / polarizer / TAC) held between protective sheets such as triacetyl cellulose (TAC).
  • TAC triacetyl cellulose
  • the pressure-sensitive adhesive composition for a polarizing plate of the present invention described above on at least one surface of a polarizing plate having a three-layer structure of TAC / polarizer / TAC, polarizing with pressure-sensitive adhesive A plate is made.
  • the composition may be applied on the polarizing plate, but is preferably applied on a protective sheet (release sheet) that is peeled off during use.
  • the application of the pressure-sensitive adhesive composition for a polarizing plate can be suitably performed by a coating method such as an immersion method, a coating method, or an ink jet method using the liquid pressure-sensitive adhesive composition for a polarizing plate. Among these, the application method is preferable.
  • the pressure-sensitive adhesive composition for polarizing plate of the present invention is coated on a protective sheet (peeling sheet) and dried to form a pressure-sensitive adhesive layer on the protective sheet.
  • a polarizing plate with an adhesive is produced by transferring and curing on the polarizing plate.
  • the pressure-sensitive adhesive composition applied on the protective sheet (release sheet) is preferably dried at 70 to 120 ° C. for about 1 to 3 minutes using a hot air dryer or the like.
  • a protective sheet for protecting the exposed surface is provided in close contact with the exposed surface of the adhesive layer provided on the polarizing plate. It is preferable.
  • a synthetic resin sheet such as polyester subjected to a release treatment with a release agent such as a fluororesin, paraffin wax, or silicone is suitable so that it can be easily peeled off from the adhesive layer. Used for.
  • the protective sheet is peeled off, and the exposed surface of the adhesive material layer is brought into close contact with the glass substrate or the like.
  • the surface protective sheet a protective film or the like that is adhesively processed on one side of a PET film is preferably used.
  • the layer thickness of the pressure-sensitive adhesive layer is not particularly limited, but is preferably 1 ⁇ m or more and 100 ⁇ m or less, more preferably 5 ⁇ m or more and 50 ⁇ m or less, and still more preferably 15 ⁇ m or more and 30 ⁇ m or less.
  • the polarizing plate with an adhesive of the present invention is applicable even when the size of the liquid crystal cell to be laminated is 19 inches wide (260 mm ⁇ 415 mm) or more.
  • the size of the liquid crystal cell is 19 inches wide (260 mm ⁇ 415 mm) or more, expansion and contraction due to the influence of heat and humidity of the polarizing plate are increased. Therefore, in the conventional polarizing plate with an adhesive, since the stress is not sufficiently suppressed when exposed to high temperature and high humidity, it occurs in the vicinity of the Bethel when the light source of a large display device (for example, a liquid crystal display device) is turned on. The occurrence of “white spots” cannot be suppressed.
  • the polarizing plate with the pressure-sensitive adhesive of the present invention since the resin design of the copolymer and the type and amount of the crosslinking agent are appropriate, the stress is suppressed even when exposed to high temperature and high humidity. It is sufficient for a liquid crystal cell having a size of 19 inches wide (260 mm ⁇ 415 mm) or larger, and may be applied to a small display device (liquid crystal display device) of less than 19 inches (or less than 10 inches). The occurrence of white spots can be suppressed by moderate stress relaxation.
  • the display device of the present invention is configured by providing a display panel for displaying an image and the above-described pressure-sensitive adhesive polarizing plate of the present invention disposed on at least one surface of the display panel.
  • the display panel include a liquid crystal display panel in which a liquid crystal compound is sealed, an organic electroluminescence display panel, and the like.
  • the polarizing plate with the pressure-sensitive adhesive of the present invention is arranged on both sides of the liquid crystal display panel so that the pressure-sensitive adhesive layer is in contact with the surface of the liquid crystal display panel (for example, the surface of the glass substrate).
  • a liquid crystal display device having a structure polarizing plate / adhesive layer / liquid crystal display panel / adhesive layer / polarizing plate structure in which polarizing plates are bonded to both surfaces of the liquid crystal display panel via an adhesive layer.
  • Acrylic copolymer A comprising a structural unit derived from an alkyl (meth) acrylate and a structural unit derived from a monomer having a carboxy group, and having a weight average molecular weight of 300,000 to 700,000. And a structural unit derived from an alkyl (meth) acrylate, a structural unit derived from a monomer having a carboxy group, and a structural unit derived from a monomer having a hydroxyl group, and the weight average molecular weight is 1,000,000.
  • the content of acrylic copolymer B that is 2,000,000 or less, acrylic copolymer A, and acrylic copolymer B with respect to a total amount of 100 parts by mass is in the range of 20 parts by mass or less.
  • An isocyanate-based crosslinking agent, and the glass transition temperature (TgA) of the acrylic copolymer A is the glass transition temperature (Tg) of the acrylic copolymer B.
  • TgA glass transition temperature
  • TgB glass transition temperature
  • the ratio (MwA / MwB) of the weight average molecular weight (MwA) of the acrylic copolymer A to the weight average molecular weight (MwB) of the acrylic copolymer B is 0.5 or less ⁇ 1 >
  • the content ratio (A / B) of the acrylic copolymer A to the acrylic copolymer B is 60/40 to 80/20 on a mass basis. It is an adhesive composition for polarizing plates as described in any one.
  • the acrylic copolymer A includes a structural unit derived from an alkyl (meth) acrylate having 1 to 4 carbon atoms, a structural unit derived from (meth) acrylic acid, and the alkyl having 1 to 4 carbon atoms.
  • the acrylic copolymer B includes a structural unit derived from an alkyl (meth) acrylate having 1 to 8 carbon atoms, a structural unit derived from (meth) acrylic acid, and a structural unit derived from hydroxyalkyl (meth) acrylate.
  • a pressure-sensitive adhesive having a polarizer and a pressure-sensitive adhesive layer formed on the polarizer by application of the pressure-sensitive adhesive composition for a polarizing plate according to any one of ⁇ 1> to ⁇ 5>. It is an attached polarizing plate.
  • a display device comprising: a display panel for displaying an image; and the polarizing plate with an adhesive according to ⁇ 6>, which is disposed on at least one surface of the display panel.
  • the weight average molecular weight was determined by gel permeation chromatography (GPC) using TSK-GEL GMHXL (styrene polymer filler made by Tosoh) as a column and converted to polystyrene according to the method described above.
  • Tg is a molar average glass transition temperature calculated using the above-described formula for calculating the glass transition temperature (Tg).
  • Example 1 Preparation of adhesive composition- As acrylic copolymer A, 189.2 parts by mass of the BA / MA / AA copolymer solution obtained in Production Example A1 (solid content of BA / MA / AA copolymer: 70.0 parts by mass) and As an acrylic copolymer B, 176.5 parts by mass of a solution of BA / MA / AA / 2HEA copolymer B1 obtained in Production Example B1 (solid content of BA / MA / AA / 2HEA copolymer: 30 0.0 part by weight), 20 parts by weight of Coronate L as an isocyanate compound (isocyanate compound produced by Nippon Polyurethane Industry Co., Ltd., active ingredient: 15 parts by weight), and 0.02 part by weight of TETRAD-X as an epoxy compound (manufactured by Mitsubishi Gas Chemical Co., Ltd.) Epoxy compound, active ingredient: 0.02 parts by mass), and silane compound (SC agent) as KBM-403 (a silane coupling agent
  • the molecular weight ratio (MwA / MwB) to (MwB) is 0.33, and the acrylic copolymer A is higher than the acrylic copolymer B with respect to Tg.
  • the pressure-sensitive adhesive composition was applied to the release agent-treated surface of the release film surface-treated with the silicone-based release agent so that the coating amount after drying was 25 g / cm 2 . Next, this was dried at 100 ° C. for 90 seconds using a hot-air circulating dryer to form an adhesive layer on the release film.
  • a polarizing base film (a laminated structure of TAC film / PVA film / TAC film by laminating cellulose triacetate (TAC) films on both sides of a polarizer mainly composed of polyvinyl alcohol (PVA) film; about 190 ⁇ m)
  • TAC cellulose triacetate
  • PVA polyvinyl alcohol
  • this laminate was subjected to autoclave treatment (50 ° C., 5 kg / cm 2 , 20 minutes), and allowed to stand at 23 ° C. and 65% RH for 24 hours. Then, it was left for 500 hours in a Dry environment (80 ° C., 0% RH) under high temperature and low humidity conditions and a WET environment (60 ° C., 90% RH) under high temperature and high humidity conditions. After the standing time had elapsed, the state of foaming and peeling was visually observed and evaluated according to the following evaluation criteria. ⁇ Evaluation criteria> A: Foaming and peeling were not observed at all. B: Foaming and peeling were hardly observed. C: Some foaming and peeling were observed. D: Foaming and peeling were noticeable.
  • Example 2 Comparative Examples 1 to 6
  • Tg, Mw the monomer composition and physical properties (Tg, Mw) of the acrylic copolymer, the weight average molecular weight, the content ratio of the acrylic copolymers A and B, and the amount of the crosslinking agent are shown in Tables 1 and 2 below.
  • a pressure-sensitive adhesive composition was prepared in the same manner as in Example 1 except that the change was made, and a polarizing film was produced and evaluated.

Abstract

La présente invention concerne une composition adhésive pour des plaques de polarisation, qui contient : un copolymère acrylique (A) qui a une masse moléculaire moyenne en poids de 300 000 à 700 000 (bornes incluses) et contient une unité constitutive issue d'un (méth)acrylate d'alkyle et une unité constitutive issue d'un monomère ayant un groupe carboxy ; un copolymère acrylique (B) qui a une masse moléculaire moyenne en poids de 1 000 000 à 2 000 000 (bornes incluses) et contient une unité constitutive issue d'un (méth)acrylate d'alkyle, une unité constitutive issue d'un monomère ayant un groupe carboxy et une unité constitutive issue d'un monomère ayant un groupe hydroxyle ; et 20 parties en masse ou moins d'un agent de réticulation à base d'isocyanate par rapport à 100 parties en masse de la quantité totale du copolymère acrylique (A) et du copolymère acrylique (B). Cette composition adhésive pour des plaques de polarisation est configurée de telle sorte que la température de transition vitreuse du copolymère acrylique (A) n'est pas inférieure à la température de transition vitreuse du copolymère acrylique (B).
PCT/JP2013/065228 2012-06-05 2013-05-31 Composition adhésive pour des plaques de polarisation, plaque de polarisation ayant un adhésif et dispositif d'affichage WO2013183563A1 (fr)

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KR1020147034956A KR102090220B1 (ko) 2012-06-05 2013-05-31 편광판용 점착제 조성물, 점착제가 부착된 편광판 및 표시 장치
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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2015151173A1 (fr) * 2014-03-31 2015-10-08 株式会社寺岡製作所 Composition adhesive et adhesif utilisant celle-ci
WO2022244886A1 (fr) * 2021-05-21 2022-11-24 日東電工株式会社 Feuille adhésive, corps stratifié optique et dispositif d'affichage d'image
WO2023068009A1 (fr) * 2021-10-18 2023-04-27 大塚化学株式会社 Matériau adhésif sensible à la pression et feuille adhésive sensible à la pression
JP7402769B2 (ja) 2020-09-07 2023-12-21 日本カーバイド工業株式会社 車両保護フィルム用粘着剤組成物及び車両保護フィルム

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP6484484B2 (ja) * 2015-03-30 2019-03-13 日本カーバイド工業株式会社 粘着剤組成物及び粘着シート
JP6511659B2 (ja) * 2015-06-08 2019-05-15 藤森工業株式会社 光学フィルム用粘着剤層、及び光学フィルム用粘着フィルム
TWI745316B (zh) 2015-11-25 2021-11-11 日商理研科技股份有限公司 門體
EP3418342A4 (fr) * 2016-02-19 2019-11-13 Riken Technos Corporation Adhésif sensible à la pression et articles le contenant
JP6497476B1 (ja) * 2018-09-20 2019-04-10 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

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH09137143A (ja) * 1995-09-14 1997-05-27 Nippon Kayaku Co Ltd 光学用粘着剤組成物
JP2000109771A (ja) * 1998-10-07 2000-04-18 Lintec Corp 粘着シート
JP2010126722A (ja) * 2008-11-26 2010-06-10 Toray Saehan Inc 光漏れ制御用粘着剤組成物及びその組成物の塗布されたディスプレイ装置用光学フィルム
JP2011231189A (ja) * 2010-04-26 2011-11-17 Nippon Carbide Ind Co Inc 偏光板用粘着剤組成物、並びにそれを用いた粘着剤付偏光板及び液晶表示装置

Family Cites Families (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3533589B2 (ja) 1997-04-09 2004-05-31 綜研化学株式会社 偏光板用粘着剤組成物および偏光板
JP2004323543A (ja) * 2003-04-21 2004-11-18 Nitto Denko Corp 光学部材用粘着剤組成物、光学部材用粘着剤層、粘着型光学部材および画像表示装置
JP4519572B2 (ja) * 2004-08-26 2010-08-04 日東電工株式会社 光学部材用粘着剤組成物、光学部材用粘着剤層およびその製造方法、粘着剤層付光学部材、ならびに画像表示装置
KR100668943B1 (ko) * 2004-04-23 2007-01-12 주식회사 엘지화학 편광판용 아크릴계 점착제 조성물
JP5269282B2 (ja) * 2004-08-11 2013-08-21 住友化学株式会社 粘着剤
JP2006309114A (ja) * 2005-03-30 2006-11-09 Lintec Corp 偏光板用粘着剤、粘着剤付き偏光板及びその製造方法
KR101202518B1 (ko) * 2008-01-15 2012-11-16 주식회사 엘지화학 점착제 조성물, 상기를 포함하는 편광판 및 액정표시장치
JPWO2010024103A1 (ja) * 2008-09-01 2012-01-26 日本カーバイド工業株式会社 粘着剤組成物、粘着剤、及び光学フィルム
MY160559A (en) * 2009-03-16 2017-03-15 Denka Company Ltd Adhesive and adhesive sheet
JP2011038055A (ja) * 2009-08-18 2011-02-24 Nippon Carbide Ind Co Inc 粘着剤組成物及び光学フィルム
JP5595034B2 (ja) * 2009-12-28 2014-09-24 リンテック株式会社 粘着性組成物、粘着剤および粘着シート
JP5555043B2 (ja) * 2010-04-26 2014-07-23 日本カーバイド工業株式会社 偏光板用粘着剤組成物、並びにそれを用いた粘着剤付偏光板及び液晶表示装置
WO2012026456A1 (fr) * 2010-08-24 2012-03-01 日本カーバイド工業株式会社 Composition d'agent adhésif
KR101351621B1 (ko) * 2010-12-29 2014-01-15 제일모직주식회사 점착제 조성물 및 이를 이용한 광학 부재

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH09137143A (ja) * 1995-09-14 1997-05-27 Nippon Kayaku Co Ltd 光学用粘着剤組成物
JP2000109771A (ja) * 1998-10-07 2000-04-18 Lintec Corp 粘着シート
JP2010126722A (ja) * 2008-11-26 2010-06-10 Toray Saehan Inc 光漏れ制御用粘着剤組成物及びその組成物の塗布されたディスプレイ装置用光学フィルム
JP2011231189A (ja) * 2010-04-26 2011-11-17 Nippon Carbide Ind Co Inc 偏光板用粘着剤組成物、並びにそれを用いた粘着剤付偏光板及び液晶表示装置

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2015151173A1 (fr) * 2014-03-31 2015-10-08 株式会社寺岡製作所 Composition adhesive et adhesif utilisant celle-ci
JP7402769B2 (ja) 2020-09-07 2023-12-21 日本カーバイド工業株式会社 車両保護フィルム用粘着剤組成物及び車両保護フィルム
WO2022244886A1 (fr) * 2021-05-21 2022-11-24 日東電工株式会社 Feuille adhésive, corps stratifié optique et dispositif d'affichage d'image
WO2023068009A1 (fr) * 2021-10-18 2023-04-27 大塚化学株式会社 Matériau adhésif sensible à la pression et feuille adhésive sensible à la pression
JP7282288B1 (ja) * 2021-10-18 2023-05-26 大塚化学株式会社 粘着材および粘着シート

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JPWO2013183563A1 (ja) 2016-01-28
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KR20150016561A (ko) 2015-02-12
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