TW201706382A - Adhesive composition for polarizing plate, adhesive layer, adhesive sheet and polarizing plate with adhesive layer - Google Patents

Abstract

The purpose of present invention is to provide an adhesive composition for polarizing plate capable of forming adhesive layer which can suppress warp (bending) of liquid crystal cell and is superior in durability. The present invention provides an adhesive composition for polarizing plate, the adhesive composition having (A) (meth)acrylic copolymer, and a gel fraction of adhesive formed from the composition of 30 mass% or less, wherein the (meth)acrylic copolymer is obtained by copolymerization of copolymerizing components including alkyl (meth)acrylate containing an alkyl group having a number of carbon atoms of 4 to 18, and branching degree of 0.55 or less detected by gel permeation chromatography method/multi-angle laser beam scattering detector (GPC-MALS).

Description

Adhesive composition for polarizing plate, adhesive layer, adhesive sheet and polarizing plate with adhesive layer

The present invention relates to an adhesive composition for a polarizing plate.

The liquid crystal cell has a structure in which a liquid crystal layer is sandwiched between two substrates (for example, a glass plate), and a polarizing plate is adhered to the surface of the substrate via an adhesive layer. The polarizing plate is susceptible to heat shrinkage in a high-temperature/high-humidity heat environment and lacks dimensional stability, so that warpage may occur on the liquid crystal cell. In recent years, with the thinning of the liquid crystal cell (for example, thinning of the substrate constituting the liquid crystal cell) and the thinning of the polarizing plate, the problem of warpage of the liquid crystal cell in a high-temperature/high-humidity heat environment has been greatly improved. The reason why the liquid crystal cell warps may be, for example, that the adhesive layer does not conform to the heat shrinkage (size change) of the polarizing plate, and the stress relaxation property of the adhesive layer is low.

At the same time, in a high-temperature/high-humidity heat environment, problems such as foaming at the interface between the polarizing plate and the substrate, breakage of the adhesive layer, and peeling of the polarizing plate are apt to occur. Therefore, in terms of an adhesive for a polarizing plate, high durability is required.

In general, a method of suppressing the warpage of the liquid crystal cell is, for example, a method of using an adhesive layer which can change the size of the polarizing plate and has high flexibility. However, such an adhesive layer may cause problems such as insufficient cohesive force, deterioration in durability, and deterioration in workability.

In the solution of the above-mentioned problem, for example, Patent Document 1 discloses that an adhesive for an optical film containing a specific (meth)acrylic polymer, a peroxide, and an isocyanate compound is subjected to a crosslinking reaction. A method of forming an adhesive layer. Patent Document 1 describes a cross-linking method using a thermal decomposition cross-linking reaction using a peroxide and a cross-linking method using an amine ester bond of an isocyanate-based compound, and the size of the accompanying optical film can be used. The varying stress maintains sufficient stress relaxation characteristics to maintain high durability.

However, in the method of Patent Document 1, since the remaining peroxide is decomposed by light or heat in the adhesive layer after the crosslinking reaction to generate radicals, the adhesive layer may also deteriorate over time. The problem.

Meanwhile, in Patent Document 2, as a problem of durability under reworkability and high-temperature/high-humidity conditions, an adhesive composition containing a (meth)acrylic monomer or a macromolecule is disclosed. a monomer and a (meth)acrylic polymer formed by polymerizing a (meth)acrylate monomer having a crosslinkable functional group, and a curing agent of a functional group reactive with the crosslinkable functional group, Further, the gel fraction is 55% or more and 80% or less.

However, in Patent Document 2, there is no description of suppressing warpage of the liquid crystal cell, and the gel fraction of the adhesive layer is also high, so The characteristics of stress relaxation are also low.

(previous technical literature) (Patent Literature)

[Patent Document 1] Japanese Patent Laid-Open Publication No. 2006-183022

[Patent Document 2] Japanese Patent Laid-Open Publication No. 2010-150400

An object of the present invention is to provide an adhesive composition for a polarizing plate, an adhesive layer formed of the above composition, an adhesive sheet for a polarizing plate containing the adhesive layer, and a polarizing layer of an adhesive layer containing the adhesive layer. In the plate, the adhesive composition for the polarizing plate can form an adhesive layer which can suppress warpage (bending) of the liquid crystal cell and is excellent in durability.

The present inventors have devoted themselves to reviewing in order to solve the above problems. As a result, it has been found that even when a (meth)acrylic copolymer obtained by copolymerization of an alkyl (meth) acrylate having an alkyl group having 4 to 18 carbon atoms and a branching degree in a specific range is used, even In the case where the designed gel fraction is low, an adhesive layer capable of suppressing warpage (bending) of the liquid crystal cell and having excellent durability can be formed. That is, the inventors of the present invention have found that the above problems can be solved by using an adhesive composition for a polarizing plate having the following specific structure, and the present invention has been completed.

The present invention is, for example, the following [1] to [10].

[1] An adhesive composition for a polarizing plate comprising (A) (methyl) propyl The olefinic copolymer, wherein the gel fraction of the adhesive formed by the composition is 30% by mass or less, and the (meth)acrylic copolymer has 4 to 18 carbon atoms (the alkyl group) The copolymerization component of a methyl methacrylate and a polymerizable macromonomer is copolymerized, and the branching degree measured by a gel permeation chromatography/multi-angle laser light scattering detector (GPC-MALS) is 0.55. the following.

[2] The adhesive composition for a polarizing plate according to the above [1], wherein the (meth)acrylic copolymer (A) is in addition to the alkyl (meth)acrylate and the polymerizable macromonomer. The copolymer obtained by copolymerizing a polar group-containing monomer.

[3] The adhesive composition for a polarizing plate according to the above [1], wherein the amount of the polar group-containing monomer in the copolymerization is 10% by mass or less based on 100% by mass of the copolymerization component. .

[4] The adhesive composition for a polarizing plate according to any one of the above [1], wherein the (meth)acrylic copolymer (A) is subjected to gel permeation chromatography (GPC method). The weight average molecular weight (Mw) measured is from 200,000 to 1,500,000.

[5] The adhesive composition for a polarizing plate according to any one of the above [1], wherein the (B) crosslinking agent is further contained.

[6] The adhesive composition for a polarizing plate according to the above [5], wherein the crosslinking agent (B) is selected from the group consisting of an isocyanate compound (B1), a metal chelator compound (B2), and an epoxy compound (B3). At least one of them.

[7] The adhesive composition for a polarizing plate according to the above [5], wherein the content of the crosslinking agent (B) is 100% based on the mass of the (meth)acrylic copolymer (A). The serving is 5 parts by mass or less.

[8] The adhesive layer for a polarizing plate is formed of the adhesive composition for a polarizing plate according to any one of the items [1] to [7], wherein the gel fraction is 30% by mass or less.

[9] An adhesive sheet for a polarizing plate comprising the adhesive layer according to the above [8].

[10] An adhesive layer-attached polarizing plate comprising a polarizing plate and an adhesive layer according to the above [8] on at least one surface of the polarizing plate.

In the present invention, an adhesive composition for a polarizing plate, an adhesive layer formed of the above composition, an adhesive sheet for a polarizing plate containing the adhesive layer, and a polarizing layer containing an adhesive layer of the adhesive layer may be provided. In the plate, the adhesive composition for the polarizing plate can form an adhesive layer which can suppress warpage (bending) of the liquid crystal cell and is excellent in durability.

Hereinafter, the adhesive composition for a polarizing plate, the adhesive layer for a polarizing plate, the adhesive sheet for a polarizing plate, and a polarizing plate with an adhesive layer will be described. In the following, the adhesive composition for a polarizing plate of the present invention may be simply referred to as "adhesive composition", and the adhesive layer for a polarizing plate of the present invention may be simply referred to as "adhesive layer", and the polarizing plate of the present invention is used. Adhesive sheets can also be referred to as "adhesive sheets".

[Adhesive Composition for Polarizing Plate]

The adhesive composition for a polarizing plate of the present invention contains a (meth)acrylic copolymer (A). The above-mentioned adhesive composition preferably further contains a crosslinking agent (B), and may contain at least one selected from the group consisting of a decane coupling agent (C), an antistatic agent (D), and an organic solvent (E). .

The adhesive formed by the adhesive composition for a polarizing plate of the present invention has a gel fraction of 30% by mass or less, preferably 0 to 25% by mass, more preferably 0 to 20% by mass. Even if the gel fraction is in the above range, as described later, since the (meth)acrylic copolymer (A) contains a high branched chain derived from a polymerizable macromonomer, the branched chain of the copolymer (A) is obtained. The layers can be appropriately overlapped with each other, so that the durability and workability of the adhesive layer are not deteriorated. When the gel fraction exceeds the above range, the stress due to the change in the size of the polarizing plate in a high-temperature/high-humidity heat environment may not be sufficiently absorbed/mitigated by the adhesive layer. The gel fraction is, for example, a value measured by an adhesive taken under the conditions described in the examples.

[(Meth)acrylic copolymer (A)]

The (meth)acrylic copolymer (A) is a copolymer obtained by copolymerizing a copolymerization component of an alkyl (meth)acrylate having a carbon number of 4 to 18 and a polymerizable macromonomer. In terms of the copolymerization component of the copolymer (A), at least one selected from the group consisting of a polar group-containing monomer and other monomers other than the above may be used.

In the present specification, acrylic acid and methacrylic acid are also collectively referred to as "(meth)acrylic acid". Meanwhile, the constituent unit derived from a certain monomer a contained in the polymer is also referred to as "monomer a unit".

(meth)acrylic copolymer (A) with gel permeation layer The branching degree measured by the analytical/multi-angle laser light scattering detector (GPC-MALS) is 0.55 or less, preferably 0.10 to 0.54, more preferably 0.20 to 0.53, and particularly preferably 0.30 to 0.53. The details of the measurement conditions of the branching degree are described in the examples.

The degree of branching can be an index, and if it is 0.55 or less, it is a branched polymer, and when it exceeds 0.55, it is a linear polymer. Further, in the branched polymer, when the value of the branching degree is small, the branching of the polymer molecule is large, and the branching degree is high, and the value of the branching degree is large, and the branch of the polymer molecule is small, indicating that the branched chain is low.

The (meth)acrylic copolymer (A) having a degree of branching in the above range may (1) often cause overlapping of branching chains of polymer molecules at room temperature or so, and as a result, even if the polymerization is designed The molecular weight of the substance and the gel fraction of the adhesive layer are low, and the storage stability of the polymer can be maintained, the adhesive property, the punching of the adhesive layer and the like, the deformation of the adhesive layer and the less prominentness, etc. (2) At high temperatures (for example, 60 ° C), the polymer molecules are soothed by some of the aforementioned overlaps, so that the adhesive layer exhibits excellent flexibility, and not only the polarizing plate warpage is well suppressed (bending) At the same time, due to the partial overlap remaining, the adhesive layer can also exhibit excellent durability.

From the viewpoint of suppressing warpage of the polarizing plate, it is presumed that it is due to the following reasons. For example, in the case of a polarizing plate/adhesive layer/adhesive body, a case where a glass plate is used as an adherend will be described as an example. The polarizing plate and the glass plate have different heat shrinkage rates, and usually the heat shrinkage rate (size change) of the polarizing plate is larger than that of the glass plate. Adhesive layer lacks softness under high temperature/high humidity environment At this time, the adhesive layer does not respond to the dimensional change of the polarizing plate, so that the stress cannot be alleviated in the adhesive layer, and the stress is concentrated on the glass plate, so that the glass plate is warped. On the other hand, the adhesive layer formed by the adhesive composition of the present invention can relax the above overlap in a high temperature/high humidity environment due to the high branched polymer, so that the adhesive layer can conform to the size change of the polarizing plate. . Thus, no stress is generated and the stress is not concentrated on the glass plate. Further, since the polarizing plate is uniformly anisotropically heat-shrinkable, the birefringence of the polarizing plate is not induced. In the case as described above, it is presumed that in the present invention, since the adhesive layer can absorb and alleviate the stress accompanying the dimensional change of the polarizing plate without causing excessive stress (load) to the glass plate, it is related to the glass plate which can be suppressed. Warping.

Since the adhesive composition of the present invention has the above characteristics, it is suitable for the bonding of the substrate constituting the liquid crystal cell and the polarizing plate. In particular, even when the thickness of the glass plate constituting the thinned liquid crystal cell is as small as about 0.10 to 1.0 mm, it is suitable for the bonding application of the substrate and the polarizing plate.

"Alkyl (meth)acrylate"

As the alkyl (meth)acrylate, an alkyl (meth)acrylate having an alkyl group of 4 to 18 may be used (CH ₂ =CR ¹ -COOR ² ; R ¹ is a hydrogen atom or a methyl group, and R ² is The alkyl group having 4 to 18 carbon atoms, wherein the alkyl group has a carbon number of 4 to 12 is preferred.

Examples of the alkyl (meth)acrylate having 4 to 18 carbon atoms of the alkyl group include, for example, n-butyl (meth)acrylate, isobutyl (meth)acrylate, and tertiary (meth)acrylate. Ester, amyl (meth)acrylate, (methyl) propyl Hexyl acrylate, heptyl (meth)acrylate, 2-ethylhexyl (meth)acrylate, octyl (meth)acrylate, isooctyl (meth)acrylate, decyl (meth)acrylate , (meth) acrylate, decyl (meth) acrylate, lauryl (meth) acrylate, stearyl (meth) acrylate, isostearyl (meth) acrylate. These may be used alone or in combination of two or more.

When 100% by mass of the copolymer component of the (meth)acrylic copolymer (A) is formed, the total number of alkyl (meth)acrylates having an alkyl group having 4 to 18 carbon atoms is excellent in adhesion and durability. From the viewpoint of the above, it is preferably 99.7 to 20% by mass, more preferably 99.4 to 30% by mass, even more preferably 98.7 to 50% by mass.

As the copolymerization component of the (meth)acrylic copolymer (A), an alkyl (meth)acrylate having an alkyl group having 1 to 3 carbon atoms (CH ₂ =CR ³ -COOR ⁴ ; R ³ is a hydrogen atom) can be used. Or a methyl group, R ⁴ is an alkyl group having 1 to 3 carbon atoms).

Examples of the alkyl (meth)acrylate having an alkyl group having 1 to 3 carbon atoms include, for example, methyl (meth)acrylate, ethyl (meth)acrylate, and n-propyl (meth)acrylate. Isopropyl methacrylate. These may be used alone or in combination of two or more.

The amount of the (meth)acrylic acid alkyl ester having 1 to 3 carbon atoms in the alkyl group is preferably 60% by mass or less, and preferably 50% by mass or less based on 100% by mass of the copolymer component. More preferably, it is more preferably 40% by mass or less.

Polymeric Macromonomer

a polymeric macromonomer having an alkyl (meth) acrylate as described above A polymerizable unsaturated group in which an ester is copolymerized, and a monomer having a large molecular weight.

The polymer chain (main chain) portion constituting the polymerizable macromonomer is not particularly limited as long as it has a polymerizable unsaturated group copolymerizable with the above (meth)acrylic acid alkyl ester, and is mainly composed of a main component. It is preferable that it is a repeating constituent unit derived from at least one selected from the group consisting of alkyl (meth)acrylate, styrene, and acrylonitrile, and the main component is a repeating constituent unit derived from an alkyl (meth)acrylate. . The main component thereof means that the content exceeds 50% by mass relative to the total repeat unit amount.

The main component of the polymer chain portion is a polymerizable macromonomer derived from a repeating constituent unit of an alkyl (meth)acrylate, and the main component is a (meth) group having a carbon number of from 1 to 8 derived from an alkyl group. The polymer chain of the repeating constituent unit of the alkyl acrylate is particularly preferred. Examples of the alkyl (meth)acrylate include methyl (meth)acrylate, ethyl (meth)acrylate, n-butyl (meth)acrylate, and isobutyl (meth)acrylate. Tert-butyl butyl methacrylate.

When the polymer chain portion is a repeating constituent unit derived from an alkyl (meth) acrylate, the content of the alkyl (meth) acrylate unit having an alkyl group having 1 to 8 carbon atoms in the polymer chain portion is usually 60% by mass or more is preferably 80% by mass or more. When the content is in this range, it may contain a repeating constituent unit derived from styrene or acrylonitrile.

The repeating constituent unit constituting the polymer chain (main chain) portion may be composed of one type of repeating constituent unit, or may be composed of two or more types of repeating constituent units. In the latter case, the polymer chain portion may be any of: a random copolymer chain, a block copolymer chain, and an alternating copolymer chain.

The polymerizable macromonomer can be reacted with the above-mentioned (meth)acrylic acid alkyl ester used as a copolymerization component, and in the (meth)acrylic copolymer (A), a side chain derived from the aforementioned macromonomer can be formed. . Thus, the (meth)acrylic copolymer (A) is a multi-branched polymer having a plurality of branched structures.

The polymerizable unsaturated group having a polymerizable macromonomer is preferably a group containing an ethylenically unsaturated double bond, and examples thereof include a (meth)acryl fluorenyl group, an allyl group, and an allyl group. The vinyl group, the vinylidene group, and the vinyl group are preferably a (meth) acrylonitrile group or a vinyl group, and a (meth) acryl fluorenyl group is particularly preferred.

The polymerizable unsaturated group may be present at the end of the polymer chain portion or in the side chain, and is preferably present at the terminal end. Further, the polymerizable unsaturated group may be present only at one end of the polymer chain portion, or may be present at both ends, but in terms of stability in polymerization, it is present only at one end of the polymer chain portion. good.

In terms of the polymerizable macromonomer, a (meth)acrylic macromonomer is preferred. Examples of the (meth)acrylic macromonomer may, for example, be a poly(methyl) acrylate having a (meth) acrylonitrile group, a poly(meth) acrylate, or a poly(meth) acrylate. The butyl ester is preferably a poly(methyl) acrylate having a (meth) acrylonitrile group at its end.

The number average molecular weight of the polymerizable macromonomer is usually 500 or more, preferably 1,000 to 10,000, more preferably 3,000 to 8,000. The number average molecular weight (Mn) of the polymerizable macromonomer is determined by gel permeation chromatography and converted to the value of polystyrene.

The glass transition temperature (Tg) of the polymerizable macromonomer is preferably from -60 to 150 ° C and from -30 to 130 ° C from the viewpoint of sufficient cohesive force and appropriate elastic properties for ensuring workability and durability. More preferably, it is preferably from 0 to 120 ° C. The glass transition temperature (Tg) of the polymerizable macromonomer can be calculated, for example, from the monomer unit constituting the polymerizable macromonomer and the ratio thereof, and the Fox formula described later.

The commercially available product of the polymerizable macromonomer may, for example, be a (meth)acryl fluorenyl group having a terminal functional group and a poly(meth)acrylic acid group in a polymer chain portion manufactured by East Asia Synthetic Co., Ltd. Molecular macromonomer of methyl ester (product name: 45% AA-6, AA-6SR, AA-6), polymer chain part is poly(butyl acrylate) macromonomer (product name: AB-6), polymerization The chain part is a polymolecular monomer of polybutyl methacrylate (product name: AW-6S).

The polymerizable macromonomer may be used singly or in combination of two or more.

In 100% by mass of the copolymerization component of the (meth)acrylic copolymer (A), the total amount of the polymerizable macromonomer is usually from 0.3 to 20% by mass, preferably from 0.5 to 12% by mass, and 0.8. More preferably 10% by mass. When the copolymerization amount of the macromonomer is within the above range, it is preferred from the viewpoint of obtaining cohesiveness of the copolymer. When the copolymerization amount of the macromonomer is more than the above range, the viscosity during copolymerization may increase rapidly. When the viscosity of the coating liquid containing the copolymer is too high, good coating properties may not be obtained for the substrate.

"Polymer-containing monomers"

Examples of the monomer having a polar group include, for example, a monomer having a hydroxyl group, and An acid group monomer, an amine group-containing monomer, a guanamine group-containing monomer, a nitrogen-containing heterocyclic monomer, and a cyano group-containing monomer. Examples of the acid group in the present specification include a carboxyl group, an acid anhydride group, a phosphoric acid group, and a sulfuric acid group. As the monomer having a polar group, a monomer containing a polar group (crosslinkable functional group) reactive with a crosslinkable functional group containing a crosslinking agent (B) is preferably used.

In order to improve the adhesion to the substrate of the optical film such as a polarizing plate, a monomer having a polar group as a carboxyl group and/or a hydroxyl group, that is, a monomer selected from a carboxyl group and a hydroxyl group-containing monomer, is used. At least one of the bodies is preferred.

The hydroxyl group-containing monomer may, for example, be a hydroxyl group-containing (meth) acrylate, and specific examples thereof include 2-hydroxyethyl (meth)acrylate and 3-hydroxypropyl (meth)acrylate. A hydroxyalkyl (meth)acrylate such as 4-hydroxybutyl (meth)acrylate, 6-hydroxyhexyl (meth)acrylate or 8-hydroxyoctyl (meth)acrylate. The hydroxyalkyl group of the hydroxyalkyl (meth) acrylate has a carbon number of usually 2 to 8, and preferably 2 to 6.

The hydroxyl group-containing monomer may be used singly or in combination of two or more.

Examples of the carboxyl group-containing monomer include, for example, β-carboxyethyl (meth)acrylate, 5-carboxypentyl (meth)acrylate, mono(meth)acryloxyethyl succinate, ω- a carboxyl group-containing (meth) acrylate such as carboxypolycaprolactone mono(meth)acrylate; acrylic acid, methacrylic acid, isaconic acid, crotonic acid, fumaric acid, maleic acid. Examples of the acid anhydride group-containing monomer include maleic anhydride and isaconic anhydride. Examples of the monomer having a phosphate group include, for example, a (meth)acrylic monomer having a phosphate group in a side chain; and a sulfate group Examples of the monomer include a (meth)acrylic monomer having a sulfuric acid group in a side chain.

For example, the acid value of the (meth)acrylic copolymer (A) is preferably 117 mgKOH/g or less, more preferably 78 mgKOH/g or less.

Examples of the amino group-containing monomer include an amino group-containing (meth) acrylate such as dimethylaminoethyl (meth)acrylate or diethylaminoethyl (meth)acrylate. Examples of the mercapto group-containing monomer include, for example, (meth)acrylamide, N-methyl-(meth)acrylamide, N-ethyl-(meth)acrylamide, N- Propyl (meth) acrylamide, N-hexyl (meth) acrylamide. Examples of the monomer containing a nitrogen-containing heterocyclic ring include vinyl pyrrolidone, acrylonitrile, and vinyl caprolactam. Examples of the cyano group-containing monomer include cyano (meth) acrylate and (meth) acrylonitrile.

The amount of the polar group-containing monomer to be used is preferably 10% by mass or less, more preferably 0.1 to 9% by mass, even more preferably 0.5 to 8% by mass, based on 100% by mass of the copolymer component.

When the amount of the polar matrix-containing monomer is less than or equal to the above upper limit, the crosslinking density of the (meth)acrylic copolymer (A) and the crosslinking agent (B) is not excessively high, and thus it is obtained. An adhesive layer excellent in stress relaxation properties. In the present invention, since a (meth)acrylic copolymer (A) having a structural unit derived from a (meth)acrylic macromonomer and having a high degree of branching is used, even if the crosslinking density is low, that is, in an adhesive The layer design is a low gel fraction of 30% by mass or less, and an adhesive layer having high processability, storage stability, and durability can also be obtained.

The polar group-containing monomer may be used alone or in combination of two or more.

Other Monomers

In the range of forming the copolymerization component of the (meth)acrylic copolymer (A), for example, a (meth)acrylic alkoxyalkyl group may be contained in a range which does not impair the physical properties of the (meth)acrylic copolymer (A). Other (meth) acrylates such as esters, alkoxypolyalkylene glycol (meth)acrylates, (meth)acrylates containing an alicyclic group or an aromatic ring group.

Examples of the alkoxyalkyl (meth)acrylate include, for example, methoxymethyl (meth)acrylate, 2-methoxyethyl (meth)acrylate, and 2-ethoxy(meth)acrylate. Ethyl ethyl ester, 3-methoxypropyl (meth)acrylate, 3-ethoxypropyl (meth)acrylate, 4-methoxybutyl (meth)acrylate, 4-(meth)acrylate Ethoxybutyl ester.

Examples of the alkoxy polyalkylene glycol mono(meth)acrylate include, for example, methoxybisethylene glycol mono(meth)acrylate, methoxydipropylene glycol mono(meth)acrylate, and a single Ethoxytriethylene glycol (meth)acrylate, ethoxydiethylene glycol mono(meth)acrylate, methoxytriethylene glycol mono(meth)acrylate.

Examples of the (meth) acrylate containing an alicyclic group or an aromatic ring group include, for example, cyclohexyl (meth)acrylate, benzyl (meth)acrylate, and phenyl (meth)acrylate.

In the above copolymerization, the total amount of the other (meth) acrylate to be used is preferably 60% by mass or less, more preferably 40% by mass or less, based on 100% by mass of the copolymer component.

Meanwhile, in the range which does not impair the physical properties of the (meth)acrylic copolymer (A), for example, styrene, methyl styrene, or the like may be used. Alkyl styrenes such as dimethyl styrene, trimethyl styrene, propyl styrene, butyl styrene, hexyl styrene, pentyl styrene and octyl styrene; fluorostyrene, chlorostyrene, bromine a styrene monomer such as styrene, dibromostyrene, iodine styrene, nitrostyrene, ethoxylated styrene or methoxystyrene; or a copolymerizable monomer such as vinyl acetate.

In the above copolymerization, the total amount of the copolymerizable monomer used is preferably 40% by mass or less, more preferably 20% by mass or less, based on 100% by mass of the copolymer component.

The other monomers may be used alone or in combination of two or more.

"Production Conditions of (Meth)Acrylic Copolymer (A)"

The (meth)acrylic copolymer (A) can be produced by a conventional polymerization method such as a solution polymerization method, a bulk polymerization method, an emulsion polymerization method or a suspension polymerization method, and a solution polymerization method is preferred. Specifically, a polymerization solvent and a copolymerization component are added to the reaction vessel, and a polymerization initiator is added in an inert gas atmosphere such as nitrogen, and then the reaction initiation temperature is usually set to 40 to 100 ° C, and 50 to 80 ° C. Preferably, the reaction temperature is usually maintained at 50 to 90 ° C, and preferably 70 to 90 ° C, and the reaction is carried out for 4 to 20 hours.

The (meth)acrylic copolymer (A) is preferably a copolymer obtained by the above copolymerization in the presence of a polymerization initiator. Examples of the polymerization initiator include an azo initiator and a peroxide polymerization initiator.

Examples of the azo initiator are, for example, 2,2'-azobisisobutyronitrile and 2,2'-azobis(4-methoxy-2,4-dimethylvaleronitrile). , 2,2'-azobis(2-cyclopropylpropionitrile), 2,2'-azobis(2,4-dimethylvaleronitrile), 2,2'-even Nitrogen di(2-methylbutyronitrile), 1,1'-azobis(cyclohexane-1-carbonitrile), 2-(aminomercaptoazo)isobutyronitrile, 2-phenylazo- 4-methoxy-2,4-dimethylvaleronitrile, 2,2'-azobis(2-amidinopropane) dihydrochloride, 2,2'-azobis(N,N'- Dimethylene isobutyl hydrazine), 2,2'-azobis[2-methyl-N-(2-hydroxyethyl)-propanamide], 2,2'-azobis(isobutyl) Guanidine) dihydrate, 4,4'-azobis(4-cyanovaleric acid), 2,2'-azobis(2-cyanopropanol), dimethyl-2,2'- An azo compound such as azobis(2-methylpropionate) or 2,2'-azobis[2-methyl-N-(2-hydroxyethyl)propanamide.

Examples of the peroxide-based polymerization initiator include, for example, tertiary butyl hydroperoxide, cumene hydroxide, bisisophenylpropyl peroxide, benzhydryl cumene, and laurel. Nonyl cumene, hexyl cumene, diisopropyl peroxydicarbonate, di-2-ethylhexyl peroxydicarbonate, tributyl butyl peroxyacetate, 2,2- Bis(4,4-di-tert-butylperoxycyclohexyl)propane, 2,2-bis(4,4-di-tripentylpentylperoxycyclohexyl)propane, 2,2-di(4, 4-di-tertiary octylperoxycyclohexyl)propane, 2,2-bis(4,4-di-α-isopropylphenylcyclohexyl)propane, 2,2-di(4,4- Di-tertiary butylperoxycyclohexyl)butane, 2,2-bis(4,4-di-tris-octyloctyloxycyclohexyl)butane.

These polymerization initiators may be used alone or in combination of two or more.

The polymerization initiator is usually used in an amount ranging from 0.001 to 5 parts by mass, and preferably from 0.005 to 3 parts by mass, based on 100 parts by mass of the copolymer component of the (meth)acryl-based copolymer (A). Further, in the above polymerization reaction, a polymerization initiator, a chain transfer agent, a copolymerization component, or the like may be appropriately added. Polymerization solvent.

Examples of the polymerization solvent in the solution polymerization include aromatic hydrocarbons such as benzene, toluene, and xylene; aliphatic hydrocarbons such as n-pentane, n-hexane, n-heptane, and n-octane; and cyclopentane and a ring. Alicyclic hydrocarbons such as hexane, cycloheptane, cyclooctane; diethyl ether, diisopropyl ether, 1,2-dimethoxyethane, dibutyl ether, tetrahydrofuran, dioxane, benzene Ethers such as methyl ether, phenyl ethyl ether, diphenyl ether; halogenated hydrocarbons such as chloroform, carbon tetrachloride, 1,2-dichloroethane, chlorobenzene; ethyl acetate, propyl acetate, butyl acetate Esters such as esters and methyl propionate; ketones such as acetone, methyl ethyl ketone, diethyl ketone, methyl isobutyl ketone, cyclohexanone; N, N-dimethylformamide, N, Amidoxime such as N-dimethylacetamide or N-methylpyrrolidone; a nitrile such as acetonitrile or benzonitrile; an anthracene such as dimethyl hydrazine or cyclobutyl hydrazine. These polymerization solvents may be used alone or in combination of two or more.

"Physical properties and content of (meth)acrylic copolymer (A)"

The weight average molecular weight (Mw) of the (meth)acrylic copolymer (A) measured by the GPC method is usually 200,000 to 1.5 million in terms of polystyrene, and preferably 400,000 to 1.3 million, and 500,000. More preferably, the copolymer (A), even if Mw is contained in the above range, contains a multi-branched chain derived from a polymerizable macromonomer, so that the branches of the copolymer (A) can be appropriately overlapped with each other. Therefore, the durability and workability of the adhesive layer can be prevented from deteriorating. In particular, when the Mw is 400,000 or more, an adhesive layer having high cohesiveness can be obtained.

The molecular weight distribution (Mw/Mn) of the (meth)acrylic copolymer (A) measured by the GPC method is usually 50 or less, preferably 30 or less. It is better to be 20 or less.

The glass transition temperature (Tg) of the (meth)acrylic copolymer (A) can be calculated, for example, by the Fox formula from the monomer units constituting the polymer and the ratio thereof. For example, the (meth)acrylic copolymer (A) can be synthesized generally at a glass transition temperature (Tg) calculated by the Fox formula of -70 to 0 ° C and more preferably -60 to -30 ° C. By using the (meth)acrylic copolymer (A) having such a glass transition temperature (Tg), an adhesive composition excellent in adhesion at normal temperature can be obtained.

Fox type: 1/Tg=(W ₁ /Tg ₁ )+(W ₂ /Tg ₂ )+...+(W _m /Tg _m )

W ₁ +W ₂ +...+W _m =1

In the formula, Tg is the glass transition temperature of the (meth)acrylic copolymer (A), and Tg ₁ , Tg ₂ , ..., Tg _m are the glass transition temperatures of the homogeneous polymers composed of the respective monomers, W ₁ , W ₂ , ..., W _m is the weight fraction of the constituent unit derived from each monomer in the above copolymer (A).

The glass transition temperature of the homogeneous polymer composed of each monomer in the above-mentioned Fox formula can be, for example, a value as described in Polymer Handbook Fourth Edition (Polymer Handbook Fourth Edition: Wiley-Interscience 2003).

The content of the (meth)acrylic copolymer (A) in the adhesive composition of the present invention is usually 50 to 100% by mass in 100% by mass of the solid matter other than the organic solvent (E) in the composition. More preferably, it is 60 to 99.999 mass%, particularly preferably 80 to 99.99 mass%. When the content of the (meth)acrylic copolymer (A) is in the above range, the performance as an adhesive can be balanced, and therefore the adhesive property is good.

[Crosslinking agent (B)]

The adhesive composition for a polarizing plate of the present invention preferably contains a crosslinking agent (B). The crosslinking agent (B) is not particularly limited as long as it is a component which can be crosslinked with a polar group derived from a polar group-containing monomer, which is contained in the (meth)acrylic copolymer (A). For example, an isocyanate compound (B1), a metal chelator compound (B2), and an epoxy compound (B3) are mentioned.

In the present invention, since the (meth)acrylic copolymer (A) containing a multi-branched chain derived from a polymerizable macromonomer is used, even if the crosslinking agent (B) is not used or used in a small amount, That is, even if the gel fraction of the adhesive layer to be designed is as low as 30% by mass or less, an adhesive layer having high processability, storage stability, and durability can be obtained.

The crosslinking agent (B) may be used alone or in combination of two or more.

In the crosslinking agent (B), it is preferred to use the isocyanate compound (B1) and/or the metal chelating agent compound (B2). The cross-linking of the (meth)acrylic copolymer (A) to form a covalent bond based on the isocyanate compound (B1), and/or the pseudo-crosslinking based on the coordinate bond of the metal chelator compound (B2) ( Pseudo crosslinking) is preferred.

In the adhesive composition of the present invention, the total content of the crosslinking agent (B) is preferably 5 parts by mass or less, and more preferably 2.5 parts by mass or less based on 100 parts by mass of the (meth)acrylic copolymer (A). Preferably, it is 0.001 to 1 part by mass, more preferably 0.01 to 0.5 part by mass. Therefore, even if the amount of the crosslinking agent (B) used is small or unused, it can be an adhesive layer having excellent adhesion, dimensional stability, and durability in a high moist heat environment.

[Isocyanate Compound (B1)]

In the case of the isocyanate compound (B1), an isocyanate compound having 2 or more isocyanate groups in one molecule is usually used. The (meth)acrylic copolymer (A) is crosslinked by the isocyanate compound (B1) to form a crosslinked body (mesh polymer).

The isocyanate compound (B1) has an isocyanate group number of usually 2 or more, preferably 2 to 8 and more preferably 3 to 6. When the number of isocyanate groups is in the above range, the point of the crosslinking reaction efficiency of the (meth)acrylic copolymer (A) and the isocyanate compound (B1) and the viewpoint of maintaining the flexibility of the pressure-sensitive adhesive layer are preferable.

Examples of the diisocyanate compound having 2 isocyanate groups in one molecule include aliphatic diisocyanate, alicyclic diisocyanate, and aromatic diisocyanate. Examples of the aliphatic diisocyanate include, for example, ethyl diisocyanate, tetramethylene diisocyanate, pentamethylene diisocyanate, hexamethylene diisocyanate, 2-methyl-1,5-pentyl An aliphatic diisocyanate having 4 to 30 carbon atoms such as an alkyl diisocyanate, 3-methyl-1,5-pentane diisocyanate or 2,2,4-trimethyl-1,6-hexamethylene diisocyanate. Examples of the alicyclic diisocyanate include isobornane diisocyanate, cyclopentyl diisocyanate, cyclohexyl diisocyanate, hydrogenated xylene diisocyanate, hydrogenated toluene diisocyanate, hydrogenated diphenylmethane diisocyanate, and hydrogenation four. An alicyclic diisocyanate having 7 to 30 carbon atoms such as methyl xylene diisocyanate. Examples of the aromatic diisocyanate include, for example, phenylene diisocyanate, toluene diisocyanate, xylene diisocyanate, naphthalene diisocyanate, diphenyl ether diisocyanate, diphenylmethane diisocyanate, An aromatic diisocyanate having 8 to 30 carbon atoms such as diphenylpropane diisocyanate.

An example of the isocyanate compound having 3 or more isocyanate groups in one molecule is, for example, an aromatic polyisocyanate. Aliphatic polyisocyanate, alicyclic polyisocyanate. Specific examples thereof include 2,4,6-triisocyanate toluene, 1,3,5-triisocyanate benzene, and 4,4',4"-triphenylmethane triisocyanate.

Meanwhile, examples of the isocyanate compound (B1) include a polymer of the above isocyanate compound having an isocyanate group number of 2 or more (for example, a 2-mer or a 3-mer, a biuret, or an isocyanuric acid). An ester), a derivative (for example, an addition reaction product of a polyhydric alcohol and two or more molecules of a diisocyanate compound), and a polymer. The polyhydric alcohol in the above derivative may, for example, be a low molecular weight polyol such as trivalent or higher alcohol such as trimethylolpropane, glycerol or neopentyl alcohol; or a high molecular weight polyol such as polyether plural. Alcohol, polyester polyol, acrylic polyol, polybutadiene polyol, polyisoprene polyol.

Examples of such an isocyanate compound include, for example, a trimer of diphenylmethane diisocyanate, a polymethylene polyphenyl polyisocyanate, a hexamethylene diisocyanate or a toluene diisocyanate biuret or a different three. a reaction product of a polycyanate body, trimethylolpropane and toluene diisocyanate or xylene diisocyanate (for example, a 3-molecular addition compound of toluene diisocyanate or xylene diisocyanate), trimethylolpropane and six A reaction product of methylene diisocyanate (for example, a 3-molecule addition compound of hexamethylene diisocyanate), a polyether polyisocyanate, or a polyester polyisocyanate.

In the isocyanate compound (B1), a reaction product of trimethylolpropane and toluene diisocyanate or xylene diisocyanate is used in the point of improving aging property and light leakage performance (L-manufactured by Soken Chemical Co., Ltd.) 45. TD-75 manufactured by Zaken Chemical Co., Ltd., hexamethylene diisocyanate or isocyanurate of isocyanurate (TSE-100 manufactured by Asahi Kasei Industrial Co., Ltd., 2050 manufactured by Japan Polyurethane Co., Ltd.) good.

The isocyanate compound (B1) may be used alone or in combination of two or more.

In the adhesive composition of the present invention, the content of the isocyanate compound (B1) is preferably 5 parts by mass or less, more preferably 2.5 parts by mass or less, based on 100 parts by mass of the (meth)acryl-based copolymer (A). It is more preferably 1 part by mass or less, and more preferably 0.5 part by mass or less. When the content is in the above range, it is more preferable that the durability and the stress relaxation property are easily balanced. The lower limit of the above (B1) is used, for example, 0.001 parts by mass, and preferably 0.01 parts by mass.

[Metal Chelating Compound (B2)]

Examples of the metal chelating agent compound (B2) include, for example, a polyvalent metal such as aluminum, iron, copper, zinc, tin, titanium, nickel, ruthenium, magnesium, vanadium, chromium or zirconium, and alkoxides and B. A compound coordinated with acetone, ethyl acetate or the like. Among them, an aluminum chelating agent compound (M-12AT manufactured by Amika Chemical Co., Ltd., etc.) is particularly preferable. Specifically, for example, aluminum isopropylate, aluminum second butyrate, ethyl acetoacetate diisopropyl alcohol, triethyl acetonitrile aluminum acetate, and aluminum tridecyl acetonate can be exemplified.

The metal chelating agent compound (B2) may be used alone or in combination of two or more.

The metal chelating agent compound (B2) can be crosslinked to the (meth)acrylic copolymer (A) (pseudocrosslinking) by a coordinate bond. When the metal chelating agent compound (B2) as the crosslinking agent (B) is used, the above-mentioned crosslinking can be maintained at room temperature, and the cohesiveness of the polymer can be exhibited, and at the high temperature, some of the above-mentioned cross-linking can be decomposed. The adhesive layer exhibits better softness.

In the adhesive composition of the present invention, the content of the metal chelating agent compound (B2) is preferably 5 parts by mass or less based on 100 parts by mass of the (meth)acrylic copolymer (A), and more preferably 2.5 parts by mass or less. Preferably, it is more preferably 1 part by mass or less, and more preferably 0.5 part by mass or less. When the content is in the above range, it is preferable that the durability and the stress relaxation property are easily balanced. The lower limit of the above (B2) is used, for example, 0.001 parts by mass, and preferably 0.01 parts by mass.

In the adhesive composition of the present invention, when the isocyanate compound (B1) and the metal chelating agent compound (B2) as the crosslinking agent (B) are used, the content of the above (B2) is 100 parts by mass based on the above (B1). It is usually more than 0 parts by mass and not more than 1000 parts by mass, more preferably more than 0 parts by mass and more preferably 600 parts by mass or less, more preferably more than 0 parts by mass and more preferably 400 parts by mass or less. When the content is in the above range, it is preferable to suppress the amount of warpage and to improve the adhesion to the substrate of the optical film such as a polarizing plate.

Epoxy Compound (B3)

In the case of the epoxy compound (B3), an epoxy compound having 2 or more epoxy groups in one molecule is usually used. For example, ethylene glycol diepoxypropyl ether, Polyethylene glycol diepoxypropyl ether, glycerol diepoxypropyl ether, glycerol triepoxypropyl ether, 1,3-bis(N,N-diepoxypropylaminomethyl) Cyclohexane, N,N,N',N'-tetraepoxypropylm-xylylenediamine, N,N,N',N'-tetraepoxypropylaminophenylmethane, heterotrimerization Triglycidyl cyanate, m-N,N-diepoxypropylaminophenyl epoxidized propyl ether, N,N-diepoxypropyltoluamide, N,N-diepoxypropyl aniline.

In the adhesive composition of the present invention, the content of the epoxy compound (B3) is preferably 2 parts by mass or less, more preferably 1 part by mass or less based on 100 parts by mass of the (meth)acrylic copolymer (A). It is more preferably 0.5 parts by mass or less. The lower limit of the above (B3) is used, for example, 0.001 parts by mass, preferably 0.01 parts by mass.

[decane coupling agent (C)]

The adhesive composition for a polarizing plate of the present invention preferably contains a decane coupling agent (C). The decane coupling agent (C) allows the adhesive layer to be firmly adhered to an adhesive such as a glass plate, thereby helping to prevent the peeling in a high moist heat environment.

Examples of the decane coupling agent (C) include a decane coupling agent containing a polymerizable unsaturated group such as vinyltrimethoxy decane, vinyltriethoxy decane or methacryloxypropyltrimethoxy decane; -glycidoxypropyltrimethoxydecane, 3-glycidoxypropyltriethoxydecane, 3-glycidoxypropylmethyldimethoxydecane, 3-epoxypropoxypropane Epoxy-containing decane coupling agent such as methyl dimethyl oxane or 2-(3,4-epoxycyclohexyl)ethyltrimethoxy decane; 3-aminopropyltrimethoxy decane, N-(2- Aminoethyl)-3-aminopropyltrimethoxyoxane, N-(2-aminoethyl)-3-aminopropylmethyldi An amine-containing decane coupling agent such as methoxy decane or a halogen-containing decane coupling agent such as 3-chloropropyltrimethoxy hydride.

The content of the decane coupling agent (C) in the adhesive composition for a polarizing plate of the present invention is usually 1 part by mass or less, and 0.01 to 1 based on 100 parts by mass of the (meth)acrylic copolymer (A). The mass fraction is preferably from 0.05 to 0.5 parts by mass. When the content is in the above range, there is a tendency to prevent peeling of the polarizing plate in a high-humidity heat environment and bleeding of the decane coupling agent (C) in a high-temperature environment.

[Antistatic agent (D)]

The antistatic agent (D) can be used for reducing the surface resistance value of the adhesive composition for a polarizing plate of the present invention. Examples of the antistatic agent (D) include a surfactant, an ionic compound, and a conductive polymer.

Examples of the surfactant include, for example, a cationic surfactant having a cationic group such as a quaternary ammonium salt, a guanamine quaternary ammonium salt, a pyridinium salt, or a primary to tertiary amine group; An anionic surfactant such as an acid group, a sulfate group or a phosphate group; an alkylbetaine, an alkylimidazolinium betaine, an alkylamine oxide, an amino acid sulfuric acid Amphoteric surfactants such as esters; glycerol fatty acid esters, sorbitan fatty acid esters, polyoxyethylene alkylamines, polyoxyethylene alkylamine fatty acid esters, N-hydroxyethyl-N-2 Nonionic surfactants such as hydroxyalkylamines and alkyldiethanolamines.

Further, as the surfactant, a reactive emulsifier containing a polymerizable group may be exemplified, and the above-mentioned surfactant or a polymer system interface containing a monomer component containing a reactive emulsifier may be used. Sex agent.

The ionic compound is composed of a cationic portion and an anionic portion, and may be either solid or liquid at room temperature (23 ° C / 50% RH).

The cation portion constituting the ionic compound may be either one of an inorganic cation or an organic cation. In terms of inorganic cations, alkali metal ions and alkaline earth metal ions are preferred, and Li ⁺ , Na ⁺ and K ⁺ excellent in antistatic properties are more preferable. Examples of the organic cations include pyridinium cations, piperidinium cations, pyrrolidinium cations, pyrroline cations, pyrrole cations, imidazolium cations, tetrahydropyrimidinium cations, dihydropyrimidinium cations, and pyrazoles. a phosphonium cation, a pyrazolinium cation, a tetraalkylammonium cation, a trialkyl phosphonium cation, a tetraalkyl phosphonium cation, and the like.

The anion portion constituting the ionic compound is not particularly limited as long as it can form an ionic bond with an ionic moiety. Specifically, for example, F ^- , Cl ^- , Br ^- , I ^- , AlCl ₄ ^- , Al ₂ Cl ₇ ^- , BF ₄ ^- , PF ₆ ^- , SCN ^- , ClO ₄ ^- , NO ₃ ^- , CH ₃ COO ^- , CF ₃ COO ^- , CH ₃ SO ₃ ^- , CF ₃ SO ₃ ^- , (CF ₃ SO ₂ ) ₂ N ^- , (F ₂ SO ₂ ) ₂ N ^- , (CF ₃ SO ₂ ) ₃ C ^- , AsF ₆ ^- , SbF ₆ ^- , NbF ₆ ^- , TaF ₆ ^- , F(HF) _n ^- , (CN) ₂ N ^- , C ₄ F ₉ SO ₃ ^- , (C ₂ F ₅ SO ₂ ) ₂ N ^- , C ₃ F ₇ COO ^- and (CF ₃ SO ₂ )(CF ₃ CO)N ^- . Among them, an anion of a fluorine atom is preferable because an ionic compound having a low melting point can be obtained, and particularly, (F ₂ SO ₂ ) ₂ N ^- and (CF ₃ SO ₂ ) ₂ N ^{- are more} preferable.

For the ionic compound, it is preferred to use, for example, lithium bis(trifluoromethanesulfonyl)imide, lithium bis(difluorosulfonyl)imide, and tris(trifluoromethanesulfonate). Mercapto) lithium methane, potassium bis(trifluoromethanesulfonyl)imide, potassium bis(difluorosulfonyl)imide, 1-ethylpyridinium hexafluorophosphate, 1-butylpyridinium hexafluorophosphate Phosphate, 1-hexyl-4-methylpyridinium hexafluorophosphate, 1-octyl-4-methylpyridinium hexafluorophosphate, 1-octyl-4-methylpyridinium di(fluorosulfonate) Imino, 1-octyl-4-methylpyridinium bis(trifluoromethanesulfonyl)imide, tetrafluoroboric acid (N,N-diethyl-N-methyl-N-(2-) Methoxyethyl)ammonium, N,N-diethyl-N-methyl-N-(2-methoxyethyl)ammonium bis(trifluoromethanesulfonyl)imide, 1-octylpyridine Fluorosulfonimide, 1-octyl-3-methylpyridinium, trifluorosulfonimide.

Examples of the conductive polymer include polythiophene, polyaniline, polypyrrole, and derivatives thereof.

The content of the antistatic agent (D) in the adhesive composition for a polarizing plate of the present invention is usually 3 parts by mass or less, and 0.01 to 3 based on 100 parts by mass of the (meth)acrylic copolymer (A). The mass fraction is preferably from 0.05 to 2.5 parts by mass.

[Organic solvent (E)]

The adhesive composition of the present invention preferably contains an organic solvent (E) in order to prepare the coating property. The organic solvent may, for example, be a polymerization solvent as described in the column of the (meth)acrylic copolymer (A). For example, a polymer solution containing the (meth)acrylic copolymer (A) obtained by the above copolymerization and a polymerization solvent may be mixed with a crosslinking agent (B) to prepare an adhesive composition. The content of the organic solvent in the adhesive composition of the present invention is usually from 50 to 90% by mass, preferably from 60 to 85% by mass.

Furthermore, the term "solids" in this specification refers to adhesion. In the components contained in the agent composition, all the components other than the organic solvent (E) are removed, and the "solid content" means the ratio of the solid matter to 100% by mass of the adhesive composition.

[additive]

The adhesive composition of the present invention may further contain, in addition to the above components, an antioxidant, a light stabilizer, a metal corrosion inhibitor, an adhesive, and a plasticizer, without departing from the effects of the present invention. One or two or more kinds of the (meth)acrylic polymer and the rework agent other than the above-mentioned (A).

[Modulation of Adhesive Composition for Polarizing Plate]

The adhesive composition for a polarizing plate of the present invention can be prepared by mixing the (meth)acrylic copolymer (A) and other components as necessary in a generally known manner. For example, a polymer solution containing the polymer obtained at the time of synthesis of the (meth)acrylic copolymer (A), and a crosslinking agent (B) and other components may be formulated as needed.

[Adhesive layer]

The adhesive layer of the present invention can be obtained, for example, by coating/drying the above-mentioned adhesive composition; or by performing a crosslinking reaction in the above adhesive composition, specifically, (meth)acrylic acid The copolymer (A) is obtained by crosslinking with a crosslinking agent (B).

Examples of the conditions for forming the adhesive layer are as follows. Will The adhesive composition of the invention is applied to a support, depending on the kind of the solvent, and is usually dried at 50 to 150 ° C, more preferably at 60 to 100 ° C, usually for 1 to 10 minutes, more preferably 2 to 7 minutes. Remove the solvent to form a coating membrane. The film thickness of the dried coating film is usually 5 to 75 μm, preferably 10 to 50 μm.

The adhesive layer is preferably formed under the following conditions. Applying the adhesive composition of the present invention to a support, and then adhering the cover film to the coating film formed under the above conditions, usually for 3 days or longer, more preferably 7 to 10 days, and usually 5 to 60 ° C. More preferably, it is cured in an environment of 15 to 40 ° C, and usually 30 to 70% RH, more preferably 40 to 70% RH. Further, crosslinking is carried out under the above-mentioned ripening conditions, and the crosslinked body (mesh polymer) can be effectively formed.

As a method of applying the adhesive composition, a generally known method such as a spin coating method, a knife coating method, a roll coating method, a bar coating method, a blade coating method, a die coating method, a gravure coating method, or the like may be used. / Drying is performed to a predetermined thickness.

Examples of the support and the cover film include a polyester film such as polyethylene terephthalate (PET); and a plastic film such as a polyolefin film such as polyethylene, polypropylene or an ethylene-vinyl acetate copolymer.

The adhesive layer formed of the adhesive composition of the present invention has a gel fraction of 30% by mass or less and 0 to 25 from the viewpoint of suppressing deformation, cohesive force, adhesion, and removability of the polarizing plate. The mass % is preferably from 0 to 20% by mass. Even if the gel fraction is in the above range, since the (meth)acrylic copolymer (A) has a multi-branched chain derived from a polymerizable macromonomer, the branches of the copolymer (A) can be appropriately cross-linked. The stacking does not reduce the durability and processability of the adhesive layer. When the gel fraction exceeds the above range, the size of the polarizing plate is caused by the high temperature/high humidity environment The varying stress can be sufficiently absorbed/mitigated by the adhesive layer.

[Adhesive sheet for polarizing plate]

The adhesive sheet for a polarizing plate of the present invention contains an adhesive layer formed of the above-mentioned adhesive composition for a polarizing plate. Examples of the adhesive sheet include, for example, a double-sided adhesive sheet containing only the above adhesive layer; a double-sided adhesive sheet comprising a substrate and the above-mentioned adhesive layer formed on both surfaces of the substrate; A single-sided adhesive sheet having the above-mentioned adhesive layer formed on one surface of the substrate; and an adhesive sheet having a release-treated cover film adhered to the surface of the adhesive sheet on which the adhesive layer is not attached to the substrate.

Examples of the substrate and the cover film include a polyester film such as polyethylene terephthalate (PET); and a plastic film such as a polyolefin film such as polyethylene, polypropylene or an ethylene-vinyl acetate copolymer.

The conditions for forming the adhesive layer and the gel fraction are the same as those described in the column of [Adhesive Layer].

The thickness of the adhesive layer is usually 5 to 75 μm from the viewpoint of maintaining adhesive properties, and preferably 10 to 50 μm. The film thickness of the substrate and the cover film is not particularly limited, but is usually 10 to 125 μm, and preferably 25 to 75 μm.

[Polarizer with Adhesive Layer]

The polarizing plate with an adhesive layer of the present invention is characterized in that it has a polarizing plate and at least one surface of the polarizing plate, and an adhesive layer formed of the adhesive composition for a polarizing plate of the present invention. In addition, in this specification, the "polarizing plate" means the "polarizing film" in use.

As the polarizing plate, a previously known polarizing film can be used. For example, a multilayer film having a stretched film obtained by further including a polarizing component on a film made of a polyvinyl alcohol-based resin and a protective film disposed on the stretched film may be mentioned. Examples of the polyvinyl alcohol-based resin include polyvinyl alcohol, polyethylene formaldehyde, polyvinyl acetal, and a saponified product of an ethylene/vinyl acetate copolymer. Examples of the polarizing component include iodine or a dichroic dye. Examples of the protective film include a cellulose film such as triethylenesulfonyl cellulose, a polycarbonate film, and a polyether ruthenium film.

The thickness of the polarizing plate is usually from 30 to 250 μm, preferably from 50 to 200 μm.

The method of forming the pressure-sensitive adhesive layer on the surface of the polarizing plate is not particularly limited, and examples thereof include a method in which the above-mentioned adhesive composition is directly applied by a bar coater or the like on the surface of the polarizing plate, and the adhesive sheet for a polarizing plate of the present invention is used. A method in which an adhesive layer is transferred onto a surface of a polarizing plate to be cooked. The conditions for drying and ripening, and the range of the gel fraction are the same as those described in the column of [Adhesive Layer].

The thickness of the adhesive layer formed on the polarizing plate is usually 5 to 75 μm, and preferably 10 to 50 μm. Further, the pressure-sensitive adhesive layer may be formed on at least one surface of the polarizing plate, and examples thereof include an aspect in which an adhesive layer is formed on only one surface of the polarizing plate, and an adhesive layer is formed on both surfaces of the polarizing plate.

Further, the polarizing plate may be further laminated with a layer having other functions such as a protective layer, an anti-glare layer, a phase difference layer, and a viewing angle enhancement layer.

Further, the pressure-sensitive adhesive layer-attached polarizing plate of the present invention obtained as described above was placed on the surface of the substrate of the liquid crystal cell to fabricate a liquid crystal element. Where the liquid crystal unit, A structure having a liquid crystal layer sandwiched between two substrates.

Examples of the substrate of the liquid crystal cell include, for example, a glass plate. The thickness of the substrate is usually 0.1 to 1 mm, and preferably 0.15 to 0.8 mm. In particular, in the present invention, the above-described adhesive composition can be used to suppress warpage of the polarizing plate and the substrate. Therefore, even if the thickness of the substrate is small (for example, 0.8 mm or less and preferably 0.15 to 0.7 mm), the polarizing plate is bonded to the substrate, and the above-described adhesive composition is also suitable.

Example

Hereinafter, the present invention will be more specifically described by the examples, but the present invention is not limited to the examples. In the following description of the examples and the like, "parts" means "parts by mass" unless otherwise specified.

[GPC and GPC-MALS]

For the (meth)acrylic polymer, the weight average molecular weight (Mw) and the number average molecular weight (Mn) were determined by gel permeation chromatography (GPC method) under the following conditions, and gel permeation chromatography was used. The multi-angle laser light scattering detector (GPC-MALS) obtains the degree of branching under the following conditions.

‧Measurement device: HLC-8320GPC (manufactured by Tosoh Co., Ltd.)

‧GPC pipe column structure: the following four pipe columns (all manufactured by Tosoh Co., Ltd.)

(1)TSKgel HxL-H (protective column)

(2) TSKgel GMHxL

(3) TSKgel GMHxL

(4)TSKgel G2500HxL

‧Flow rate: 1.0mL/min

‧column temperature: 40 ° C

‧ Sample concentration: 1.5% (w / v) (diluted with tetrahydrofuran)

‧Mobile phase solvent: tetrahydrofuran

‧Detector: DAWN HELEOS (MALS detector) + Optilab rEX (RI detector)

‧ Convert standard polystyrene (when measuring Mw and Mn)

[Synthesis Example 1]

In a reaction apparatus equipped with a stirrer, a circulation condenser, a thermometer, and a nitrogen introduction tube, 98 parts of n-butyl acrylate and a methyl methacrylate group containing a methyl methacrylate group (trade name: AA-6) were added. Manufactured by East Asia Synthetic Co., Ltd., Tg: 105 ° C, Mn: 6,000) 1 part, 1 part of 4-hydroxybutyl acrylate, and 100 parts of ethyl acetate solvent, and the temperature was raised to 80 ° C under introduction of nitrogen. Next, 0.1 part of 2,2'-azobisisobutyronitrile was further added, and polymerization was carried out for 6 hours at 80 ° C in a nitrogen atmosphere. After the completion of the reaction, the mixture was diluted with ethyl acetate to prepare a polymer solution having a solid concentration of 30% by mass. The obtained (meth)acrylic copolymer A had a weight average molecular weight (Mw) of 700,000, a molecular weight distribution (Mw/Mn) of 7.2, a branching degree of 0.54, and an acid value of 0 mgKOH/g.

[Synthesis Examples 2 to 14]

A polymer solution having a solid concentration of 30% by mass was prepared in the same manner as in Synthesis Example 1, except that the copolymerization component and the polymerization initiator used in the polymerization reaction were changed as described in Table 1. The results are shown in Table 1.

As shown in Table 1, the MMA macromonomer is a methyl methacrylate macromonomer containing a methacryl fluorenyl group at the end (trade name: AA-6, manufactured by East Asia Synthetic Co., Ltd., Tg: 105 ° C, Mn: 6,000), BA macromonomer, butyl acrylate macromonomer containing propylene fluorenyl group at the end (trade name: AB-6, East Asia) Synthetic (manufactured), Tg: -50 ° C, Mn: 6,000).

[Example 1]

(1) Modulation of adhesive composition

The (meth)acrylic polymer solution (solid content: 30% by mass) obtained in Synthesis Example 1 was mixed with 100 parts (solid content) of the (meth)acrylic polymer contained in the solution. "TD-75" (solid content: 75 mass%, ethyl acetate solution), 0.08 parts (solid content), and "KBM" manufactured by Shin-Etsu Chemical Co., Ltd., which is a decane coupling agent, manufactured by the Institute of Chemicals Co., Ltd. -403" (solid content: 100%): 0.2 parts, and "AS-804" (solid content: 100%) manufactured by the first industrial pharmaceutical company as an antistatic agent, one part, and an adhesive composition was obtained.

(2) Making of adhesive sheets

After defoaming, the adhesive composition obtained in the above (1) was applied onto the peeled polyethylene terephthalate film (PET film) by a doctor blade, and dried at 90 ° C for 3 minutes to form a dry film. A coating film having a film thickness of 20 μm. Then, on the opposite side of the adhesive surface of the PET film of the coating film, the PET film which has been subjected to the release treatment is adhered, and then allowed to stand in a 23° C./50% RH environment for 7 days to be matured, thereby obtaining 2 tablets. The PET film was adhered to an adhesive sheet of a thickness of 20 μm.

(3) Production of polarizing plate with adhesive layer

After defoaming, the adhesive composition obtained in the above (1) was applied onto the peeled polyethylene terephthalate film (PET film) by a doctor blade, and dried at 90 ° C for 3 minutes to form A sheet of a coating film having a film thickness of 20 μm was dried. Thereafter, the sheet and the polarizing plate (thickness: 110 μm, layer composition: triethylenesulfonated cellulose film/polyvinyl alcohol film/triethylenesulfonated cellulose film), before The coating film and the polarizing plate are adhered to each other, and then allowed to stand for 7 days in a 23° C./50% RH environment to obtain an adhesive layer containing a PET film and an adhesive layer having a thickness of 20 μm and a polarizing plate. Layer of polarizing plate.

[Examples 2 to 14, Comparative Examples 1 to 3]

In the first embodiment, the same procedure as in the first embodiment was carried out except that the (meth)acrylic polymer solution was changed to the polymer solution obtained in Synthesis Examples 2 to 14 and/or the composition of the formulation was changed as shown in Table 2. Operation, obtaining an adhesive composition, an adhesive sheet, and a polarizing plate with an adhesive layer. In Table 2, M-12AT is a "M-12AT" (solid content: 10% by mass, toluene, acetonitrile acetone solution) produced by the comprehensive chemistry of the metal chelating agent compound.

[rating]

[Gel fraction]

First, from the adhesive sheet obtained in the example/comparative example, about 0.1 g of the adhesive was collected in a sample bottle, and after adding 30 mL of ethyl acetate and shaking for 4 hours, the contents of the sample bottle were made of 200 mesh stainless steel. The metal mesh was filtered, and the residue on the metal mesh was dried at 100 ° C for 2 hours and then the dry weight was measured. Then, the gel fraction of the adhesive was determined by the following formula. ‧gel fraction (%) = (dry weight / adhesive collection weight) × 100 (%)

[potential change (Creep) value]

First, the polarizing plate (the laminated film composed of the PET film/adhesive layer/polarizing plate) with the adhesive layer obtained in the experimental example/comparative example was cut into a width of 10 mm×length 100 mm, and the peeled PET was peeled off. The film is attached to the glass plate by the above-mentioned adhesive layer on the alkali-treated glass plate, and is adhered in such a manner that the adhesive area is 10 mm×10 mm. Adhesive processing polarizing plate test piece for evaluation.

Thereafter, the test piece for adhesion measurement of the polarizing plate was subjected to autoclaving (50 ° C, 5 atm), and allowed to stand in an environment of 23 ° C / 50% RH for 24 hours. Next, the test piece was fixed to the fixing clip portion in the body of the micro-dense measuring machine BOX with a length of 15 mm. Thereafter, the tensile load was 800 g and the stretching time was 1000 seconds, and the evaluation of the test piece was carried out by adhering the polarizing plate to the longitudinal direction of the polarizing plate in parallel with the bonding surface of the polarizing plate and the glass plate. The offset distance (μm) of the adhesion between the glass plate and the polarizing plate in the test piece was measured as a latent value.

[Measurement of adhesion]

First, the polarizing plate (the laminated film composed of the PET film/adhesive layer/polarizing plate) with the adhesive layer obtained in the experimental example/comparative example was cut into a size of 70 mm × 25 mm to prepare a test piece. Then, the PET film was peeled off from the test piece, and the laminated body composed of the adhesive layer/polarizing plate was adhered to one side of the glass plate having a thickness of 2 mm by a bonding machine roller so that the adhesive layer and the glass plate were joined. The obtained laminate was kept in an autoclave adjusted to 50 ° C / 5 atm for 20 minutes. Next, after standing for 1 hour in an environment of 23 ° C / 50% RH, the edge portion of the polarizing plate was stretched at a speed of 300 mm / min in a direction of 90 ° with respect to the surface of the glass plate to measure the adhesion (peeling strength).

[bending (warping)]

First, the polarizing plate (the laminated film composed of the PET film/adhesive layer/polarizing plate) with the adhesive layer obtained in the experimental example/comparative example was cut into a size of 35 mm × 400 mm (the direction of the extending axis) to prepare a test piece. Then by experiment The PET film is peeled off, and the laminated body of the adhesive layer/polarizing plate is placed on one side of the glass plate having a thickness of 0.7 mm and 40 mm×410 mm by means of a bonding machine roller to connect the adhesive layer and the glass plate. Paste. The obtained laminate was allowed to stand in an environment of 23 ° C / 50% RH for 24 hours, and then kept in an autoclave at 60 ° C for 72 hours. Thereafter, the end of one of the ends was fixed to the wall surface facing the plate surface, and the amount of the opposite end projection was measured with a ruler. The measurement was carried out at the time of taking out from the autoclave and 24 hours later.

[Endurance test]

First, the polarizing plate (the laminated film composed of the PET film/adhesive layer/polarizing plate) with the adhesive layer obtained in the experimental example/comparative example was cut into a size of 150 mm × 250 mm to prepare a test piece. Then, the PET film was peeled off from the test piece, and the laminated body composed of the adhesive layer/polarizing plate was adhered to one side of the glass plate having a thickness of 2 mm by a bonding machine roller so that the adhesive layer and the glass plate were joined. The obtained laminate was further held in an autoclave adjusted to 50 ° C / 5 atm for 20 minutes to prepare a test plate. And made the same test plate 2 pieces. Then, the test plate was placed under conditions of a temperature of 80 ° C (heat resistance) or a temperature of 60 ° C / humidity of 90% RH (moisture resistance) for 500 hours, and then the foaming and breaking in the adhesive layer were observed. Occurs and is assessed on the basis of the following criteria. The foaming system occurs when the cohesive force is insufficient, and the fracture system occurs when the stress relaxation is insufficient.

(bubble)

‧AA: No foaming at all.

‧BB: The area of foaming is less than 5% of the total.

‧CC: The area of foaming is 5% or more of the total.

(fracture)

‧AA: No breaks at all.

‧BB: The area of the break is less than 5% of the total.

‧CC: The area of the fracture is more than 5% of the total.

In the composition of Comparative Example 2, a (meth)acrylic copolymer having a degree of branching of 0.59 or a high gel fraction of 57% by mass was used, so that the bending evaluation after 24 hours was poor (5.0). Although it is determined that there is no blistering in terms of durability evaluation, it is often broken.

In the composition of Comparative Example 3, a (meth)acrylic copolymer having a degree of branching of 0.59 was used, and the gel fraction was designed to have a gel fraction of 0% by mass. Therefore, foaming often occurred in the evaluation of durability.

In the composition of Comparative Example 1, although the (meth)acrylic copolymer having a branching degree of 0.54 was designed to have a high gel fraction of 65% by mass, the bending evaluation after 24 hours could not be satisfied ( 5.0 mm or more), although no blistering was determined in terms of durability evaluation, but fracture occurred frequently.

On the other hand, in the composition of the examples, a (meth)acrylic copolymer containing a constituent unit derived from a (meth)acrylic macromonomer and having a degree of branching of 0.55 or less was used, and was designed to be coagulated. Since the gel fraction is 30% by mass or less, the bending evaluation after 24 hours is good (3.5 mm or less), and the foaming and breaking occurring in the durability evaluation are within an allowable range.

Claims (10)

An adhesive composition for a polarizing plate comprising (A) a (meth)acrylic copolymer, wherein a gel fraction of the adhesive formed by the composition is 30% by mass or less, and the (meth) The acrylic copolymer is obtained by copolymerization of a copolymerization component of an alkyl group-containing (meth)acrylic acid alkyl group having 4 to 18 carbon atoms and a polymerizable macromonomer, and is subjected to gel permeation chromatography/multi-angle Ray The branching degree measured by the light scattering scatter detector (GPC-MALS) was 0.55 or less. The adhesive composition for a polarizing plate according to claim 1, wherein the (meth)acrylic copolymer (A) is in addition to the alkyl (meth)acrylate and the polymerizable macromonomer. A copolymer obtained by copolymerizing a polar group-containing monomer. The adhesive composition for a polarizing plate according to the first aspect of the invention, wherein the amount of the polar group-containing monomer used in the copolymerization is 10% by mass or less based on 100% by mass of the copolymerization component. The adhesive composition for a polarizing plate according to the first or second aspect of the invention, wherein the (meth)acrylic copolymer (A) has a weight measured by gel permeation chromatography (GPC method). The average molecular weight (Mw) is from 200,000 to 1.5 million. The adhesive composition for a polarizing plate according to claim 1 or 2, further comprising (B) a crosslinking agent. The adhesive composition for a polarizing plate according to claim 5, wherein the crosslinking agent (B) is selected from the group consisting of an isocyanate compound (B1), a metal chelator compound (B2), and an epoxy compound (B3). At least 1 in Kind. The adhesive composition for a polarizing plate according to claim 5, wherein the content of the crosslinking agent (B) is 5 parts by mass based on 100 parts by mass of the (meth)acrylic copolymer (A). the following. An adhesive layer for a polarizing plate is formed of the adhesive composition for a polarizing plate according to any one of claims 1 to 7, and has a gel fraction of 30% by mass or less. An adhesive sheet for a polarizing plate, which comprises the adhesive layer described in claim 8 of the patent application. A polarizing plate with an adhesive layer comprising: a polarizing plate; and an adhesive layer according to claim 8 on at least one side of the polarizing plate.