JP6019910B2 - Adhesive composition, adhesive sheet, optical film with adhesive, and optical laminate - Google Patents

Description

  The present invention relates to a pressure-sensitive adhesive composition suitable for an optical film, and a pressure-sensitive adhesive sheet and an optical film with a pressure-sensitive adhesive using the same. The optical film targeted in the present invention includes, for example, a polarizing plate and a retardation film. The present invention also relates to an optical laminate in which this optical film with an adhesive is laminated on a glass substrate and is suitably used for liquid crystal display.

  A polarizing plate is widely used by being mounted on a liquid crystal display device. A polarizing plate generally has a transparent protective film laminated on both sides of a polarizing film, a pressure-sensitive adhesive layer is formed on the surface of at least one protective film, and a release film is stuck on the pressure-sensitive adhesive layer. doing. In addition, a retardation film is laminated on a polarizing plate in which a protective film is bonded to both sides of the polarizing film to form an elliptical polarizing plate, and an adhesive layer / release film is attached in this order to the retardation film side. Sometimes. Furthermore, an adhesive layer / release film may be stuck in this order on the surface of the retardation film. In this specification, the polarizing plate, the elliptically polarizing plate, the retardation film and the like provided with the pressure-sensitive adhesive layer are collectively referred to as an optical film. Prior to bonding to the liquid crystal cell, the optical film provided with these pressure-sensitive adhesive layers is cut into a predetermined size, and then the release film is peeled off and bonded to the liquid crystal cell via the exposed pressure-sensitive adhesive layer. It will be. An optical film provided with such a pressure-sensitive adhesive layer has a problem of workability that the pressure-sensitive adhesive layer tends to be chipped during cutting. For this reason, after forming the pressure-sensitive adhesive layer, it is generally cured and used for a sufficient period of time, and there is still room for improvement in terms of productivity.

  The pressure-sensitive adhesive applied to the optical film is manufactured by copolymerizing a monomer having an acrylic ester as a main component and a polar functional group such as a hydroxyl group or a carboxyl group from the viewpoint of transparency and weather resistance. Many acrylic resins are used. By blending such an acrylic resin with a crosslinking agent, the required cohesive force is imparted. Here, the crosslinking agent is a compound having in the molecule at least two functional groups capable of forming a crosslinked structure by reacting with a polar functional group constituting an acrylic resin. Specifically, an isocyanate compound or an epoxy compound is used. Compounds, metal chelate compounds, amine compounds, and the like. Of these, isocyanate compounds are widely used as crosslinking agents.

  That is, by blending an acrylic resin having a polar functional group with an isocyanate-based crosslinking agent having at least two isocyanato groups (—NCO) in the molecule, the functional group in the acrylic resin becomes an isocyanate group in the crosslinking agent over time. Reacts with to form a cross-linked structure, develops cohesive force and improves processability. Therefore, if the speed of the cross-linking reaction is increased, the time required to show sufficient processability can be shortened. As a means for increasing the speed of the crosslinking reaction, for example, paragraph 0046 of Japanese Patent No. 4370888 (Patent Document 1) describes that an amine compound is blended as a crosslinking catalyst. It is said that a compound based on this type is suitable.

  JP-A-2009-173772 (Patent Document 2) discloses a pressure-sensitive adhesive for optical members that exhibits good processability by blending an acrylic resin having a hydroxyl group with a silane compound having an amino group and an isocyanate-based crosslinking agent. It has been proposed to provide an agent composition. Furthermore, JP-A-2009-215528 (Patent Document 3) discloses an isocyanate-based cross-linking agent and a silane coupling to an acrylic resin having an aromatic ring and a small amount of an amino group, and additionally having a carboxyl group and / or a hydroxyl group. It has been proposed that a pressure-sensitive adhesive composition for an optical film that also exhibits good processability is formulated by blending an agent.

  As described above, if a compound having an amino group or an acrylic resin having an amino group is used as one component of the pressure-sensitive adhesive composition, the pressure-sensitive adhesive having an amino group as a constituent component can be promoted although the crosslinking reaction of the pressure-sensitive adhesive can be promoted. When the composition comes into contact with a certain type of release film, the amino group reacts with the release agent in the release film, and the pressure-sensitive adhesive sheet formed from the pressure-sensitive adhesive composition adheres firmly to the release film. Therefore, there is a problem that the release film may not be peeled off.

  Moreover, each of these components constituting the pressure-sensitive adhesive composition is mixed in a state dissolved in a solvent to form a solution, and then applied onto a suitable substrate and dried to obtain a pressure-sensitive adhesive sheet. At that time, in order to keep the applicability constant, there is a demand for a solution having a small viscosity change.

  On the other hand, an optical film with an adhesive is bonded to a liquid crystal cell on the adhesive layer side to form a liquid crystal panel. In this state, it is placed under high temperature or high temperature and high humidity conditions, and heating and cooling are repeated. When the dimensional change of the optical film occurs, foaming occurs in the pressure-sensitive adhesive layer, or floating or peeling occurs between the optical film and the pressure-sensitive adhesive layer or between the pressure-sensitive adhesive layer and the liquid crystal cell glass. Therefore, it is required to have excellent durability without causing such problems. In addition, when exposed to high temperatures, the distribution of residual stress acting on the optical film becomes non-uniform and stress concentration occurs on the outer periphery of the optical film, resulting in a phenomenon called whitening that causes the outer periphery to become whitish when displaying black. Or the occurrence of color unevenness may occur, and suppression of such white spots and color unevenness is also required. Furthermore, when there is a defect when the optical film with the adhesive is bonded to the liquid crystal cell, the optical film will be peeled off once and then a new film will be attached again. A so-called rework property is also required that the layer is peeled off along with the optical film, no adhesive remains on the cell glass, and no fogging occurs.

Japanese Patent No. 4370888 (Japanese Patent Laid-Open No. 2004-190012) JP 2009-173772 A JP 2009-215528 A

  The problem of the present invention is that the change in viscosity is small in the solution state and the applicability is good, and after forming the pressure-sensitive adhesive layer, the curing time required until processing such as cutting can be performed without problems is short. Pressure-sensitive adhesive sheet or pressure-sensitive adhesive optical film, and a pressure-sensitive adhesive composition that gives a pressure-sensitive adhesive optical film excellent in durability and reworkability, and a pressure-sensitive adhesive sheet and pressure-sensitive adhesive using the same An optical film with a pressure-sensitive adhesive is provided, and the optical film with an adhesive is bonded to a glass substrate having a liquid crystal cell as a representative example to provide an optical laminate.

  As a result of intensive studies to solve such problems, the present inventors have (meth) acrylic acid ester as a main component, a (meth) acrylic monomer having a hydroxyl group, and a main chain by polymerization. A predetermined amount of each of a crosslinking agent and an organic acid is blended into an acrylic resin obtained by copolymerization of a monomer mixture containing a (meth) acrylic acid ester monomer having a carboxyl group at a position away from a predetermined number of atoms. By this, it discovered that the adhesive composition with little viscosity change in a solution state was obtained. Moreover, when this adhesive composition was formed in the sheet form, it came to show a high gel fraction in short curing time, and it discovered that the adhesive sheet excellent in workability was obtained. Furthermore, it has been found that if this pressure-sensitive adhesive sheet is provided on the surface of the optical film as a pressure-sensitive adhesive layer, an optical film with a pressure-sensitive adhesive excellent in workability, durability and reworkability can be obtained. The present invention has been completed based on such findings.

  That is, the pressure-sensitive adhesive composition of the present invention comprises the following (meth) acrylic acid ester (A-1) 94.8 to 99.89% by weight, and a (meth) acrylic monomer (A-2) having a hydroxyl group. A copolymer obtained from a monomer mixture containing 0.1 to 5% by weight and 0.01 to 0.2% by weight of a carboxyl group-containing (meth) acrylic acid ester (A-3) shown below. Containing 100 parts by weight of an acrylic resin (A) having a weight average molecular weight of 500,000 to 2,000,000, 0.01 to 5 parts by weight of a crosslinking agent (B) and 0.03 to 5 parts by weight of an organic acid (C) It is.

The (meth) acrylic acid ester (A-1) is represented by the following formula (I), wherein R ₁ represents a hydrogen atom or a methyl group; R ₂ is an alkyl group or an aralkyl group having 14 or less carbon atoms. It represents a hydrogen atom constituting these groups may be substituted with a group _{-O- (C 2 H 4 O)} n -R 3, where n is an integer of 0 or 1 to 4 , R ₃ represents an alkyl group or aryl group having 12 or less carbon atoms.

The carboxyl group-containing (meth) acrylic acid ester (A-3) is represented by the following formula (II), where R ₄ represents a hydrogen atom or a methyl group; A is 2 having 2 to 4 carbon atoms. Represents a valent organic group.

  A suitable example of the carboxyl group-containing (meth) acrylic acid ester (A-3) is 2-carboxyethyl acrylate.

In these pressure-sensitive adhesive compositions, the crosslinking agent (B) preferably contains an isocyanate compound. The organic acid (C) is preferably a carboxylic acid represented by the following formula (III), wherein R ₅ represents a hydrogen atom or an alkyl or alkenyl group having 4 or less carbon atoms.

  These pressure-sensitive adhesive compositions can further contain a silane compound (D), and the preferred amount is in the range of 0.03 to 2 parts by weight.

  The pressure-sensitive adhesive sheet of the present invention is formed from one of the above pressure-sensitive adhesive compositions into a sheet shape. Since the above-mentioned pressure-sensitive adhesive composition generally exists in a state dissolved in a solvent, the pressure-sensitive adhesive sheet is obtained by applying this pressure-sensitive adhesive composition (solution) on a suitable substrate and removing the solvent by drying. can get.

  In this pressure-sensitive adhesive sheet, the ratio of the gel fraction one day after the pressure-sensitive adhesive composition was coated in a sheet shape with respect to the gel fraction eight days after the pressure-sensitive adhesive composition was coated in a sheet form was 0.00. It can be made to be 8 or more. In addition, this pressure-sensitive adhesive sheet has a ratio of the gel fraction 4 days after the pressure-sensitive adhesive composition is coated in a sheet shape to the gel fraction 8 days after the pressure-sensitive adhesive composition is coated in a sheet shape. It can be set to 0.97 or more.

  In general, these pressure-sensitive adhesive sheets are preferably formed on a plastic film, and a typical example of the plastic film in that case is a release film subjected to a release treatment.

  Moreover, the optical film with an adhesive of the present invention is one in which any of the above adhesive sheets is bonded to the optical film. This optical film advantageously includes at least one of a polarizing plate and a retardation film.

  Furthermore, the optical layered body of the present invention is such that the optical film with an adhesive is laminated on a glass substrate on the adhesive sheet side.

  The pressure-sensitive adhesive composition of the present invention is excellent in applicability because the organic acid (C) is blended in the solution state, so that the viscosity change hardly occurs. The pressure-sensitive adhesive composition is mainly composed of an acrylic resin (A) containing a (meth) acrylic acid ester (A-3) having a carboxyl group at a position away from a site that becomes a main chain by polymerization as a constituent component. As a component, the crosslinking agent (B) is blended in it, so that the crosslinking reaction proceeds quickly, and the curing time from the application of the adhesive composition to a sheet shape until reaching a predetermined gel fraction is obtained. Since it can shorten, the workability of the formed adhesive sheet improves.

  The optical film with pressure-sensitive adhesive of the present invention is excellent in workability as described above, and once laminated on a glass substrate, if there is some trouble, even if it is peeled off from the glass substrate together with the pressure-sensitive adhesive, the glass after peeling Adhesive residue and fogging hardly occur on the surface of the substrate, and it can be used again as a glass substrate, and has excellent reworkability.

  For example, this optical film with an adhesive is laminated on a glass substrate of a liquid crystal cell to give an optical laminate for liquid crystal display. In this optical laminate, the pressure-sensitive adhesive sheet absorbs and relaxes stress caused by the dimensional change of the optical film and the glass substrate under high-temperature conditions, wet heat conditions, or in an environment where heating and cooling are repeated. Stress concentration is reduced, and the pressure-sensitive adhesive layer is prevented from floating or peeling off from the glass substrate. In addition, stress concentration when exposed to high temperatures can be prevented, and the occurrence of white spots and color unevenness can be suppressed.

It is a cross-sectional schematic diagram which shows the example of the suitable layer structure of the optical laminated body which concerns on this invention.

  Hereinafter, the present invention will be described in detail. The pressure-sensitive adhesive composition of the present invention contains an acrylic resin (A), a crosslinking agent (B) and an organic acid (C). First, each component which comprises an adhesive composition is demonstrated.

[Acrylic resin (A)]
The acrylic resin (A) constituting the pressure-sensitive adhesive composition of the present invention has a structural unit derived from the (meth) acrylic acid ester (A-1) represented by the formula (I) as a main component, and further has a hydroxyl group. A structural unit derived from the (meth) acrylic monomer (A-2) and a structural unit derived from the carboxyl group-containing (meth) acrylic acid ester (A-3) represented by the formula (II). It is a waste. Here, (meth) acrylic acid means that either acrylic acid or methacrylic acid may be used, and “(meth)” when referred to as (meth) acrylate or the like has the same meaning. In this specification, the (meth) acrylic acid ester (A-1) represented by the formula (I) is simply referred to as “monomer (A-1)” and a (meth) acrylic monomer having a hydroxyl group ( A-2) is simply referred to as “monomer (A-2)”, and the carboxyl group-containing (meth) acrylic acid ester (A-3) represented by the formula (II) is simply referred to as “monomer (A- 3) ”may be called.

In the formula (I), which is the main structural unit of the acrylic resin (A), R ₁ is a hydrogen atom or a methyl group, and R ₂ is an alkyl group or an aralkyl group having 14 or less carbon atoms. In the alkyl group or aralkyl group represented by R ₂ , each hydrogen atom may be substituted with a group —O— (C ₂ H ₄ O) _n —R ₃ . Here, n represents 0 or an integer of 1 to 4, and R ₃ represents an alkyl group or aryl group having 12 or less carbon atoms.

Among the monomers (A-1), as R ₂ in the formula (I) is an unsubstituted alkyl group, specifically, methyl acrylate, ethyl acrylate, propyl acrylate, n-acrylate Linear alkyl acrylates such as butyl, n-octyl acrylate, and lauryl acrylate; branched alkyl acrylates such as isobutyl acrylate, 2-ethylhexyl acrylate, and isooctyl acrylate; Linear alkyl methacrylates such as methyl methacrylate, ethyl methacrylate, propyl methacrylate, n-butyl methacrylate, n-octyl methacrylate, and lauryl methacrylate; and isobutyl methacrylate, 2-methacrylic acid 2- Such as ethylhexyl and isooctyl methacrylate Branched alkyl methacrylate are exemplified.

  Among these, n-butyl acrylate is preferable. Specifically, among all the monomers constituting the acrylic resin (A), n-butyl acrylate is 50% by weight or more and is described above. It is preferable to use it so as to satisfy the regulations regarding the monomer (A-1).

Further, among the monomers (A-1), specific examples of R ₂ in the formula (I) being an aralkyl group include benzyl acrylate and benzyl methacrylate.

Next, in the monomer (A-1), the hydrogen atom of the alkyl group or aralkyl group constituting R ₂ in the formula (I) is substituted with the group —O— (C ₂ H ₄ O) _n —R ₃ . I will explain what is being done. In this group —O— (C ₂ H ₄ O) _n —R ₃ , n is 0 or an integer of 1 to 4 as defined above, but 0, 1 or 2 is particularly preferable. R _{3 is} also an alkyl group or aryl group having 12 or less carbon atoms, as defined above, and may be linear or branched as long as the alkyl group has 3 or more carbon atoms. Examples of the aryl group constituting R ₃ include phenyl and naphthyl, as well as nuclear alkyl-substituted phenyl and biphenylyl (or phenylphenyl) including tolyl, xylyl, ethylphenyl and the like. R ₃ is particularly preferably these aryl groups.

Among the monomers (A-1), R ₂ in the formula (I) is an alkyl group, and the hydrogen atom is substituted with a group —O— (C ₂ H ₄ O) _n —R _3. Specifically, 2-methoxyethyl acrylate, ethoxymethyl acrylate, 2-phenoxyethyl acrylate, 2- (2-phenoxyethoxy) ethyl acrylate, and 2- (o-phenylphenoxy) ethyl acrylate Such as alkoxyalkyl-, aryloxyalkyl- or aryloxyethoxyalkyl-esters of acrylic acid; 2-methoxyethyl methacrylate, ethoxymethyl methacrylate, 2-phenoxyethyl methacrylate, 2- (2-phenoxyethoxy) methacrylate Alcohols of methacrylic acid such as ethyl and 2- (o-phenylphenoxy) ethyl methacrylate Shiarukiru -, aryloxyalkyl - or aryloxy ethoxyalkyl - such esters are exemplified.

These monomers (A-1) can be used alone or in combination with a plurality of different monomers. As described above, the monomer (A-1) is particularly preferably composed mainly of n-butyl acrylate, but in addition, other (meth) acrylic acid esters corresponding to the formula (I) Copolymerization is also effective. As a suitable composition of the monomer (A-1), among all the monomers constituting the acrylic resin (A), n-butyl acrylate is 50% by weight or more. In the formula (I), R ₂ is a hydrogen atom of the group —O— (C ₂ H ₄ O) _n —R ₃ (where n and R ₃ are as defined above). And (meth) acrylic acid ester which is an alkyl group substituted with 3) to 15% by weight.

  The monomer (A-2) is a (meth) acrylic monomer having a hydroxyl group. Examples thereof include 2-hydroxyethyl (meth) acrylate, 3-hydroxypropyl (meth) acrylate, ( Examples include 4-hydroxybutyl (meth) acrylate and 2- (2-hydroxyethoxy) ethyl (meth) acrylate. Among these, it is preferable to use 2-hydroxyethyl acrylate as one of the monomers (A-2) constituting the acrylic resin (A).

The monomer (A-3) is represented by the formula (II). In this formula (II), R ₄ is a hydrogen atom or a methyl group, and A is a divalent organic group having 2 to 4 carbon atoms. The divalent organic group represented by A is typically alkylene, which is also preferably linear alkylene, but the (meth) acrylic acid moiety CH ₂ ═C (R ₄ ) COO— Assuming that the carbon chain connecting the terminal carboxyl group —COOH is at least 2 in series, the chain may be branched if it has 3 or more carbon atoms. Among the formulas (II), acrylates are preferable, and specific examples include 2-carboxyethyl acrylate, 3-carboxypropyl acrylate, 4-carboxybutyl acrylate, and the like. Of course, the compound which changed these acrylic acid ester into the methacrylic acid ester can also become a monomer (A-3).

  2-Carboxyethyl acrylate is usually produced by dimerization of acrylic acid. In that case, in addition to 2-carboxyethyl acrylate, which is the main component, acrylic acid itself and oligomers of trimers of acrylic acid or more. In many cases, it is sold as a mixture as it is. Thus, it is of course possible to copolymerize other carboxyl group-containing (meth) acrylic monomers together with the carboxyl group-containing (meth) acrylic acid ester (A-3) represented by the formula (II). Absent.

  In the acrylic resin (A) defined in the present invention, the content of the structural unit derived from the (meth) acrylic acid ester represented by the formula (I), that is, the monomer (A-1) is 94.8. The content of the structural unit derived from the (meth) acrylic monomer (A-2) having a hydroxyl group is 0.1 to 5% by weight, and the above formula ( The content of the structural unit derived from the carboxyl group-containing (meth) acrylic acid ester represented by II), that is, the monomer (A-3) is 0.01 to 0.2% by weight. By copolymerizing the monomers (A-1), (A-2) and (A-3) in such a limited ratio, a pressure-sensitive adhesive composition giving a pressure-sensitive adhesive sheet excellent in processability is obtained. be able to. The content of the structural unit derived from the monomer (A-1) is preferably 95% by weight or more, particularly 96% by weight or more, and preferably 99.5% by weight or less. The content of the structural unit derived from the monomer (A-2) is preferably 0.5% by weight or more, and preferably 4% by weight or less, especially 3% by weight or less. Furthermore, the content of the structural unit derived from the monomer (A-3) is preferably 0.18% by weight or less, particularly 0.15% by weight or less. Of course, the total amount of structural units derived from each of the monomers (A-1), (A-2) and (A-3) does not exceed 100% by weight.

  The acrylic resin (A) used in the present invention may contain structural units derived from monomers other than the monomers (A-1), (A-2) and (A-3) described above. Good. Examples of monomers other than monomers (A-1), (A-2) and (A-3) include unsaturated monomers other than formula (II) having polar functional groups other than hydroxyl groups. , (Meth) acrylic acid ester having an alicyclic structure in the molecule, styrene monomer, vinyl monomer, (meth) acrylamide derivative, monomer having a plurality of (meth) acryloyl groups in the molecule and so on.

  An unsaturated monomer other than the formula (II) having a polar functional group other than a hydroxyl group will be described. The polar functional group other than the hydroxyl group here can be a free carboxyl group, a heterocyclic group including an epoxy ring, or the like. The acrylic acid itself and the trimer or higher oligomer of acrylic acid described above for the monomer (A-3) correspond to unsaturated monomers other than the formula (II) having a free carboxyl group. Examples of the unsaturated monomer having a heterocyclic group include acryloylmorpholine, vinyl caprolactam, N-vinyl-2-pyrrolidone, tetrahydrofurfuryl (meth) acrylate, caprolactone-modified tetrahydrofurfuryl acrylate, 3,4 -Epoxycyclohexylmethyl (meth) acrylate, glycidyl (meth) acrylate and the like.

  When an unsaturated monomer having a polar functional group other than a hydroxyl group is copolymerized, the (meth) acrylic monomer (A-2) having a hydroxyl group as an essential component and the carboxyl represented by the above formula (II) Including the group-containing (meth) acrylic acid ester (A-3), the total amount of unsaturated monomers having a polar functional group is 5% by weight based on all monomers constituting the acrylic resin (A). In the following, it is further preferable that the content is 4% by weight or less, particularly 3% by weight or less.

  Next, (meth) acrylic acid ester having an alicyclic structure in the molecule will be described. The alicyclic structure is a cycloparaffin structure having usually 5 or more carbon atoms, preferably about 5 to 7 carbon atoms. Specific examples of the acrylate ester having an alicyclic structure include isobornyl acrylate, cyclohexyl acrylate, dicyclopentanyl acrylate, cyclododecyl acrylate, methylcyclohexyl acrylate, trimethylcyclohexyl acrylate, tert-acrylate Examples include butyl cyclohexyl, α-ethoxy acrylate cyclohexyl, cyclohexyl phenyl acrylate, and the like. Specific examples of the methacrylic acid ester having an alicyclic structure include isobornyl methacrylate, cyclohexyl methacrylate, dicyclopentanyl methacrylate, cyclododecyl methacrylate, methyl cyclohexyl methacrylate, trimethyl cyclohexyl methacrylate, methacrylic acid. Examples include tert-butylcyclohexyl and cyclohexylphenyl methacrylate.

  Examples of styrenic monomers include styrene, methyl styrene, dimethyl styrene, trimethyl styrene, ethyl styrene, diethyl styrene, triethyl styrene, propyl styrene, butyl styrene, hexyl styrene, heptyl styrene, and octyl styrene. Alkyl styrenes; halogenated styrenes such as fluorostyrene, chlorostyrene, bromostyrene, dibromostyrene, and iodostyrene; and nitrostyrene, acetylstyrene, methoxystyrene, divinylbenzene, and the like.

  Examples of vinyl monomers include vinyl acetate, vinyl propionate, vinyl butyrate, vinyl 2-ethylhexanoate and vinyl laurate such as vinyl esters; vinyl halides such as vinyl chloride and vinyl bromide; Vinylidene halides such as vinylidene chloride; nitrogen-containing aromatic vinyls such as vinylpyridine, vinylpyrrolidone, and vinylcarbazole; conjugated diene monomers such as butadiene, isoprene, and chloroprene; and acrylonitrile, methacrylonitrile, etc. .

  Examples of (meth) acrylamide derivatives include N-methylol (meth) acrylamide, N- (2-hydroxyethyl) (meth) acrylamide, N- (3-hydroxypropyl) (meth) acrylamide, N- (4- Hydroxybutyl) (meth) acrylamide, N- (5-hydroxypentyl) (meth) acrylamide, N- (6-hydroxyhexyl) (meth) acrylamide, N- (methoxymethyl) (meth) acrylamide, N- (ethoxymethyl) ) (Meth) acrylamide, N- (propoxymethyl) (meth) acrylamide, N- (butoxymethyl) (meth) acrylamide, N, N-dimethyl (meth) acrylamide, N, N-diethyl (meth) acrylamide, N- Isopropyl (meth) acrylamide, N- (3-di Tilaminopropyl) (meth) acrylamide, N- (1,1-dimethyl-3-oxobutyl) (meth) acrylamide, N- [2- (2-oxo-1-imidazolidinyl) ethyl] (meth) acrylamide, 2- And acryloylamino-2-methyl-1-propanesulfonic acid.

  Examples of monomers having a plurality of (meth) acryloyl groups in the molecule include 1,4-butanediol di (meth) acrylate, 1,6-hexanediol di (meth) acrylate, and 1,9-nonane. Two diols in the molecule, such as diol di (meth) acrylate, ethylene glycol di (meth) acrylate, diethylene glycol di (meth) acrylate, tetraethylene glycol di (meth) acrylate, and tripropylene glycol di (meth) acrylate A monomer having a (meth) acryloyl group; and a monomer having three (meth) acryloyl groups in the molecule, such as trimethylolpropane tri (meth) acrylate.

  When copolymerizing a monomer other than the monomers (A-1), (A-2) and (A-3), which are essential components of the acrylic resin (A), and having no polar functional group, The amount is usually 5% by weight or less, more preferably 3% by weight or less, and particularly preferably 1% by weight or less, based on the total monomers constituting the acrylic resin (A).

  The resin component constituting the pressure-sensitive adhesive composition is the (meth) acrylic acid ester represented by the formula (I) described above, that is, the monomer (A-1), the (meth) acrylic monomer having a hydroxyl group. Two types of acrylic resin (A) having a structural unit derived from each of (A-2) and carboxyl group-containing (meth) acrylic acid ester represented by formula (II), that is, monomer (A-3) A mixture of the above may be used. Alternatively, an acrylic resin different from the acrylic resin (A) having structural units derived from the monomers (A-1), (A-2) and (A-3) at a predetermined ratio may be mixed. Good. Examples of the different acrylic resins mixed in this case include those having a structural unit derived from the (meth) acrylic acid ester of the formula (I) and having no polar functional group. The acrylic resin (A) having a predetermined proportion of structural units derived from the monomers (A-1), (A-2) and (A-3) is 80% by weight or more of the whole acrylic resin, It is preferable to be 90% by weight or more.

  The acrylic resin (A) obtained by copolymerization of the monomer mixture containing the monomers (A-1), (A-2) and (A-3) is a standard by gel permeation chromatography (GPC). A polystyrene having a weight average molecular weight Mw in the range of 500,000 to 2,000,000 is employed. The weight average molecular weight Mw is particularly preferably 500,000 to 1,700,000. When the weight average molecular weight in terms of standard polystyrene is 500,000 or more, the adhesiveness under high temperature and high humidity is improved, and the possibility of occurrence of floating or peeling between the glass substrate and the pressure sensitive adhesive sheet is reduced. And reworkability tends to be improved. In addition, when the weight average molecular weight is 2 million or less, even if the dimension of the optical film bonded to the pressure-sensitive adhesive sheet changes, the pressure-sensitive adhesive layer fluctuates following the dimensional change, so the liquid crystal cell This is preferable because there is no difference between the brightness of the peripheral edge and the brightness of the central portion, and white spots and color unevenness tend to be suppressed. The molecular weight distribution represented by the ratio Mw / Mn of the weight average molecular weight Mw and the number average molecular weight Mn is not particularly limited, but is preferably in the range of about 3 to 7, for example.

  Moreover, it is preferable that the glass transition temperature of this acrylic resin (A) exists in the range of -10 ~ -60 degreeC for adhesive expression. The glass transition temperature of the resin can be measured by a differential scanning calorimeter.

  The acrylic resin (A) can be produced by various known methods such as a solution polymerization method, an emulsion polymerization method, a bulk polymerization method, and a suspension polymerization method. In the production of this acrylic resin, a polymerization initiator is usually used. The polymerization initiator is used in an amount of about 0.001 to 5 parts by weight with respect to a total of 100 parts by weight of all monomers used in the production of the acrylic resin.

  As the polymerization initiator, a thermal polymerization initiator, a photopolymerization initiator, or the like is used. Examples of the photopolymerization initiator include 4- (2-hydroxyethoxy) phenyl (2-hydroxy-2-propyl) ketone. Examples of the thermal polymerization initiator include 2,2′-azobisisobutyronitrile, 2,2′-azobis (2-methylbutyronitrile), 1,1′-azobis (cyclohexane-1-carbonitrile), 2,2'-azobis (2,4-dimethylvaleronitrile), 2,2'-azobis (2,4-dimethyl-4-methoxyvaleronitrile), dimethyl-2,2'-azobis (2-methylpropio) And azo compounds such as 2,2'-azobis (2-hydroxymethylpropionitrile); lauryl peroxide, tert-butyl hydroperoxide, benzoyl peroxide, tert-butyl peroxybenzoate, cumene hydroper Oxide, diisopropylperoxydicarbonate, dipropylperoxydicarbonate, tert-butylperoxide Organic peroxides such as xineodecanoate, tert-butyl peroxypivalate, and (3,5,5-trimethylhexanoyl) peroxide; inorganic peroxides such as potassium persulfate, ammonium persulfate, and hydrogen peroxide An oxide etc. can be mentioned. A redox initiator using a peroxide and a reducing agent in combination can also be used as the polymerization initiator.

  As a method for producing the acrylic resin, the solution polymerization method is preferable among the methods shown above. A specific example of the solution polymerization method will be described. A desired monomer and an organic solvent are mixed, a thermal polymerization initiator is added under a nitrogen atmosphere, and about 40 to 90 ° C, preferably 50 to 80 ° C. A method of stirring at about C for about 3 to 15 hours can be mentioned. Moreover, in order to control reaction, you may add a monomer and a thermal-polymerization initiator continuously or intermittently during superposition | polymerization, or may be added in the state melt | dissolved in the organic solvent. Examples of the organic solvent include aromatic hydrocarbons such as toluene and xylene; esters such as ethyl acetate and butyl acetate; aliphatic alcohols such as propyl alcohol and isopropyl alcohol; acetone, methyl ethyl ketone, and methyl isobutyl. Ketones such as ketones can be used.

[Crosslinking agent (B)]
A crosslinking agent (B) and organic acid (C) are mix | blended with the above acrylic resins (A), and it is set as an adhesive composition. The crosslinking agent (B) is a compound having at least two functional groups in the molecule that can react with a hydroxyl group or a carboxyl group, which are polar functional groups in the acrylic resin (A), to crosslink the acrylic resin. Examples of the compound include an isocyanate compound, an epoxy compound, a metal chelate compound, and an aziridine compound.

  Isocyanate compounds are compounds having at least two isocyanato groups (-NCO) in the molecule, such as tolylene diisocyanate, hexamethylene diisocyanate, isophorone diisocyanate, xylylene diisocyanate, hydrogenated xylylene diisocyanate, diphenylmethane diisocyanate, Examples thereof include hydrogenated diphenylmethane diisocyanate, naphthalene diisocyanate, and triphenylmethane triisocyanate. In addition, adducts obtained by reacting these isocyanate compounds with polyols such as glycerol and trimethylolpropane, and those obtained by making the isocyanate compounds into dimers, trimers, and the like can also be used as crosslinking agents for pressure-sensitive adhesives. Two or more isocyanate compounds can be mixed and used.

  The epoxy compound is a compound having at least two epoxy groups in the molecule, for example, bisphenol A type epoxy resin, ethylene glycol diglycidyl ether, polyethylene glycol diglycidyl ether, glycerin diglycidyl ether, glycerin triglycidyl ether. 1,6-hexanediol diglycidyl ether, trimethylolpropane triglycidyl ether, N, N-diglycidylaniline, N, N, N ′, N′-tetraglycidyl-m-xylenediamine and the like. Two or more types of epoxy compounds can be mixed and used.

  Examples of the metal chelate compound include compounds in which acetylacetone or ethyl acetoacetate is coordinated to a polyvalent metal such as aluminum, iron, copper, zinc, tin, titanium, nickel, antimony, magnesium, vanadium, chromium and zirconium. Can be mentioned.

  An aziridine-based compound is a compound having at least two skeletons of a three-membered ring composed of one nitrogen atom and two carbon atoms, also called ethyleneimine, for example, diphenylmethane-4,4′-bis ( 1-aziridinecarboxamide), toluene-2,4-bis (1-aziridinecarboxamide), triethylenemelamine, isophthaloylbis-1- (2-methylaziridine), tris-1-aziridinylphosphine oxide, hexamethylene -1,6-bis (1-aziridinecarboxamide), trimethylolpropane tris-β-aziridinylpropionate, tetramethylolmethane tris-β-aziridinylpropionate, and the like.

  Among these crosslinking agents, isocyanate compounds, especially xylylene diisocyanate, tolylene diisocyanate or hexamethylene diisocyanate, or adducts obtained by reacting these isocyanate compounds with polyols such as glycerol and trimethylolpropane, and isocyanate compounds A dimer, trimer or the like, or a mixture of these isocyanate compounds is preferably used.

  Particularly suitable isocyanate compounds include tolylene diisocyanate, an adduct obtained by reacting tolylene diisocyanate with a polyol, a dimer of tolylene diisocyanate, and a trimer of tolylene diisocyanate.

  A crosslinking agent (B) is mix | blended in the ratio of 0.01-5 weight part with respect to 100 weight part of acrylic resins (A). The amount of the crosslinking agent (B) is preferably about 0.1 to 3 parts by weight, more preferably about 0.1 to 1 part by weight, with respect to 100 parts by weight of the acrylic resin (A). The amount of the crosslinking agent (B) with respect to 100 parts by weight of the acrylic resin (A) is preferably 0.01 parts by weight or more, particularly preferably 0.1 parts by weight or more, because the durability of the pressure-sensitive adhesive sheet tends to be improved. Moreover, when it is 5 parts by weight or less, it is preferable because white spots are not noticeable when the optical film with an adhesive is applied to a liquid crystal display device.

[Organic acid (C)]
The organic acid (C) blended in the pressure-sensitive adhesive composition is preferably a carboxylic acid represented by the formula (III). The organic acid (C) is preferably volatilized when the adhesive composition is applied on a suitable substrate and then dried.

R ₅ in the formula (III) is a hydrogen atom or an alkyl or alkenyl group having 4 or less carbon atoms. Examples of such carboxylic acids include formic acid, acetic acid, propionic acid, butyric acid, acrylic acid, methacrylic acid, crotonic acid, isocrotonic acid, vinyl acetic acid and the like. Among these, formic acid, acetic acid, acrylic acid or methacrylic acid is preferable from the viewpoint of volatility.

  An organic acid (C) is mix | blended in the ratio of 0.03-5 weight part with respect to 100 weight part of acrylic resins (A). The compounding amount of the organic acid (C) is preferably 0.05 parts by weight or more, particularly 0.1 parts by weight or more with respect to 100 parts by weight of the acrylic resin (A). Moreover, it is preferably 2 parts by weight or less, particularly 1.5 parts by weight or less with respect to 100 parts by weight of the acrylic resin (A). If the amount of the organic acid (C) relative to 100 parts by weight of the acrylic resin (A) is 0.03 parts by weight or more, particularly 0.1 parts by weight or more, the change in viscosity of the pressure-sensitive adhesive composition in the solution state becomes small. It is preferable that it is 5 parts by weight or less because the organic acid (C) hardly remains in the pressure-sensitive adhesive sheet after drying.

[Silane compound (D)]
The pressure-sensitive adhesive composition of the present invention preferably contains a silane compound (D) in order to improve the adhesion between the pressure-sensitive adhesive sheet or the pressure-sensitive adhesive-coated optical film and the glass substrate. It is preferable to blend the silane compound (D) with the acrylic resin before blending the agent.

  Examples of the silane compound (D) include vinyltrimethoxysilane, vinyltriethoxysilane, vinyltris (2-methoxyethoxy) silane, 3-glycidoxypropyltrimethoxysilane, 3-glycidoxypropylmethyldimethoxysilane, 2- (3,4-epoxycyclohexyl) ethyltrimethoxysilane, 3-chloropropylmethyldimethoxysilane, 3-chloropropyltrimethoxysilane, 3-methacryloyloxypropyltrimethoxysilane, 3-mercaptopropyltrimethoxysilane, 3- Examples include glycidoxypropyltrimethoxysilane, 3-glycidoxypropyltriethoxysilane, 3-glycidoxypropyldimethoxymethylsilane, and 3-glycidoxypropylethoxydimethylsilane. Two or more silane compounds (D) may be used.

  The silane compound (D) may be of a silicone oligomer type. When the silicone oligomer is shown in the form of (monomer)-(monomer) copolymer, for example, the following can be mentioned.

  3-mercaptopropyltrimethoxysilane-tetramethoxysilane copolymer, 3-mercaptopropyltrimethoxysilane-tetraethoxysilane copolymer, 3-mercaptopropyltriethoxysilane-tetramethoxysilane copolymer, and 3-mercaptopropyltriethoxysilane-tetraethoxy A copolymer containing a mercaptopropyl group, such as a silane copolymer;

  Mercaptomethyl groups such as mercaptomethyltrimethoxysilane-tetramethoxysilane copolymer, mercaptomethyltrimethoxysilane-tetraethoxysilane copolymer, mercaptomethyltriethoxysilane-tetramethoxysilane copolymer, and mercaptomethyltriethoxysilane-tetraethoxysilane copolymer. Containing copolymers;

  3-methacryloyloxypropyltrimethoxysilane-tetramethoxysilane copolymer, 3-methacryloyloxypropyltrimethoxysilane-tetraethoxysilane copolymer, 3-methacryloyloxypropyltriethoxysilane-tetramethoxysilane copolymer, 3-methacryloyloxypropyltriethoxysilane -Tetraethoxysilane copolymer, 3-methacryloyloxypropylmethyldimethoxysilane-tetramethoxysilane copolymer, 3-methacryloyloxypropylmethyldimethoxysilane-tetraethoxysilane copolymer, 3-methacryloyloxypropylmethyldiethoxysilane-tetramethoxysilane copolymer, and 3-Methacryloyloxypropylmethyldiethoxysilane-tetra Toki bell Ranco polymers such as, methacryloyloxypropyl group containing copolymers;

  3-acryloyloxypropyltrimethoxysilane-tetramethoxysilane copolymer, 3-acryloyloxypropyltrimethoxysilane-tetraethoxysilane copolymer, 3-acryloyloxypropyltriethoxysilane-tetramethoxysilane copolymer, 3-acryloyloxypropyltriethoxysilane -Tetraethoxysilane copolymer, 3-acryloyloxypropylmethyldimethoxysilane-tetramethoxysilane copolymer, 3-acryloyloxypropylmethyldimethoxysilane-tetraethoxysilane copolymer, 3-acryloyloxypropylmethyldiethoxysilane-tetramethoxysilane copolymer, and 3-acryloyloxypropylmethyldiethoxysilane-tetraethoxysilane Rimmer such as, acryloyloxypropyl group-containing copolymer;

  Vinyltrimethoxysilane-tetramethoxysilane copolymer, vinyltrimethoxysilane-tetraethoxysilane copolymer, vinyltriethoxysilane-tetramethoxysilane copolymer, vinyltriethoxysilane-tetraethoxysilane copolymer, vinylmethyldimethoxysilane-tetramethoxysilane copolymer, Vinyl group-containing copolymers such as vinylmethyldimethoxysilane-tetraethoxysilane copolymer, vinylmethyldiethoxysilane-tetramethoxysilane copolymer, and vinylmethyldiethoxysilane-tetraethoxysilane copolymer.

  These silane-based compounds are often liquids. The compounding amount of the silane compound (D) in the pressure-sensitive adhesive composition is usually about 0.01 to 10 parts by weight, preferably 0.02 to 2 parts by weight with respect to 100 parts by weight of the solid content of the acrylic resin (A). Parts, more preferably 0.03 to 1 part by weight. When the amount of the silane compound relative to 100 parts by weight of the acrylic resin (A) is 0.01 parts by weight or more, particularly 0.03 parts by weight or more, adhesion between the pressure-sensitive adhesive sheet and the glass substrate is improved. To preferred. Further, the amount is preferably 10 parts by weight or less, particularly 2 parts by weight or less, or 1 part by weight or less because the silane compound tends to be suppressed from bleeding out from the pressure-sensitive adhesive sheet.

[Preparation of pressure-sensitive adhesive composition]
Each component demonstrated above is mixed in the state melt | dissolved in the solvent, and is set as an adhesive composition. Here, examples of the solvent include aromatic hydrocarbons such as toluene and xylene; esters such as ethyl acetate and butyl acetate; aliphatic alcohols such as propyl alcohol and isopropyl alcohol; acetone, methyl ethyl ketone, and methyl isobutyl ketone. Ketones such as can be used. This pressure-sensitive adhesive composition exhibits good performance, but it preferably does not contain an amino group in order to avoid strong adhesion when it comes into contact with a specific release film. In particular, it is preferable not to have a tertiary amino group.

  The pressure-sensitive adhesive composition dissolved in the above solvent is coated on a suitable substrate and dried to form a pressure-sensitive adhesive sheet. The substrate used here is generally a plastic film, and a typical example thereof is a release film that has been subjected to a release treatment. The release film is, for example, a film on which a pressure-sensitive adhesive sheet of a film made of various resins such as polyethylene terephthalate, polybutylene terephthalate, polycarbonate, and polyarylate is formed and subjected to a release treatment such as a silicone treatment. be able to.

The pressure-sensitive adhesive composition (solution) of the present invention is applied on a suitable substrate, and then the pressure-sensitive adhesive sheet is formed by drying and removing the solvent. Therefore, it is preferable that the change in viscosity in the solution state is small. . The viscosity change can be defined by the following formula using the viscosity η ₁ immediately after the preparation of the pressure-sensitive adhesive composition and the viscosity η ₂ after 6 hours from the preparation.
Viscosity change (%) = (η ₂ −η ₁ ) / η ₁ × 100

  The viscosity change defined by this formula is preferably 20% or less, more preferably 15% or less, and particularly preferably 10% or less. It is preferable that the viscosity change of the pressure-sensitive adhesive composition in a solution state is 20% or less because the applicability of the solution is good. Here, the viscosity is a value measured under the condition of 12 rpm using a No. 2 spindle with an analog viscometer (LVT) manufactured by Brookfield.

  The adhesive composition in the solution state further contains a crosslinking catalyst, an antistatic agent, a weather resistance stabilizer, a tackifier, a plasticizer, a softener, a dye, a pigment, an inorganic filler, a resin other than the acrylic resin (A), and the like. May be. Among these, there are those that do not dissolve in the solvent constituting the pressure-sensitive adhesive composition and disperse, but even if some of the components are dispersed, the above discussion on viscosity can be similarly applied. If a cross-linking catalyst is blended with the cross-linking agent in the pressure-sensitive adhesive composition, the pressure-sensitive adhesive sheet can be prepared by a short time curing, and the resulting optical film with the pressure-sensitive adhesive floats between the optical film and the pressure-sensitive adhesive sheet. Occurrence of peeling or foaming in the pressure-sensitive adhesive sheet can be suppressed, and reworkability can be further improved.

  Furthermore, it is also useful to blend an ultraviolet curable compound into this pressure-sensitive adhesive composition and to cure it by irradiating with ultraviolet rays after forming the pressure-sensitive adhesive sheet to form a harder pressure-sensitive adhesive layer.

[Adhesive sheet]
As described above, the pressure-sensitive adhesive sheet of the present invention is formed into a sheet shape from the pressure-sensitive adhesive composition described above. The pressure-sensitive adhesive sheet was applied to the sheet and then allowed to stand at room temperature for 8 days. The pressure-sensitive adhesive composition was then applied to the sheet and left for 1 day at room temperature. The ratio of the subsequent gel fraction can be 0.8 or more. When this ratio is 0.8 or more, it means that the crosslinking reaction proceeds rapidly after coating in a sheet form, and the curing of the pressure-sensitive adhesive is proceeding considerably on the next day. That is, the ratio of the gel fraction is a measure of the curing rate. In addition, the gel after the adhesive composition was coated in a sheet form and then allowed to stand at room temperature for 4 days after the adhesive composition was applied in a sheet form and then allowed to stand at room temperature for 8 days The ratio of the fractions can be 0.97 or more. When this ratio is 0.97 or more, it means that the curing of the pressure-sensitive adhesive is almost completed at the fourth day. That is, the ratio of the gel fraction is a measure of the workability of the pressure-sensitive adhesive sheet. Satisfying both of these, i.e., after coating the adhesive composition into a sheet and then leaving it at room temperature for 8 days, after coating it into a sheet and leaving it at room temperature for 1 day It is more preferable that the ratio of the gel fraction becomes 0.8 or more, and the ratio of the gel fraction after standing for 4 days at room temperature after coating in a sheet form becomes 0.97 or more.

Here, the gel fraction is a value measured according to the following (1) to (4).
(1) An adhesive sheet having an area of about 8 cm × about 8 cm and a metal mesh made of SUS304 (with a weight of Wm) of about 10 cm × about 10 cm are bonded.
(2) Weigh the bonded product obtained in (1) above, weigh it Ws, then fold it 4 times so as to wrap the adhesive sheet, weigh it with a stapler (stapler), weigh it, Let the weight be Wb.
(3) The mesh stapled in (2) above is placed in a glass container, and 60 mL of ethyl acetate is added and immersed, and then the glass container is stored at room temperature for 3 days.
(4) The mesh is taken out from the glass container, dried at 120 ° C. for 24 hours, weighed, the weight is taken as Wa, and the gel fraction is calculated based on the following formula.
Gel fraction (% by weight) = [{Wa− (Wb−Ws) −Wm} / (Ws−Wm)] × 100

  As described above, the pressure-sensitive adhesive sheet is often used after being cured for a certain amount of time after being manufactured and in a state in which a crosslinking reaction is advanced to exhibit a certain degree of gel fraction. Thus, the gel fraction in the state in which the crosslinking reaction has proceeded, that is, in the state in which the curing has been completed, is, for example, the type of the acrylic resin (A) that is an active ingredient of the pressure-sensitive adhesive composition that forms it and the crosslinking agent. It can be adjusted by the amount. Specifically, the amount of the monomer having a polar functional group including the monomer (A-2) and the monomer (A-3) in the acrylic resin (A) is increased, or the pressure-sensitive adhesive composition If the amount of the cross-linking agent (B) in the product is increased, the gel fraction is increased. Therefore, the gel fraction may be adjusted by adjusting these amounts.

[Optical film with adhesive]
The optical film with pressure-sensitive adhesive of the present invention is obtained by bonding a pressure-sensitive adhesive sheet formed from the above pressure-sensitive adhesive composition to at least one surface of an optical film. In this way, in the optical film with the pressure-sensitive adhesive in a state where the pressure-sensitive adhesive sheet is bonded to the optical film, or in the optical laminate in which the pressure-sensitive adhesive sheet is further laminated on the glass substrate, the layer of the pressure-sensitive adhesive sheet is simply referred to in this specification. Sometimes referred to as “adhesive layer”. The optical film used for the optical film with an adhesive is a film having optical properties, and examples thereof include a polarizing plate and a retardation film.

  A polarizing plate is an optical film having a function of emitting polarized light with respect to incident light such as natural light. The polarizing plate absorbs linearly polarized light having a vibrating surface in a certain direction and reflects linearly polarized light having a vibrating surface in a certain direction, and reflects linearly polarized light having a vibrating surface in a certain direction. There are a polarizing separation plate having a property of transmitting linearly polarized light having a vibration plane orthogonal to the polarizing plate, an elliptically polarizing plate in which a polarizing plate and a retardation film described later are laminated. As a suitable specific example of a polarizing film that expresses the function of a polarizing plate, particularly a linear polarizing plate (sometimes called a polarizer), two colors such as iodine and a dichroic dye are applied to a uniaxially stretched polyvinyl alcohol resin film. The thing which the adsorptive orientation of the property pigment is mentioned.

  The retardation film is an optical film exhibiting optical anisotropy, for example, polyvinyl alcohol, polycarbonate, polyester, polyarylate, polyimide, polyolefin, cyclic polyolefin, polystyrene, polysulfone, polyethersulfone, polyvinylidene fluoride. / Stretched film obtained by stretching polymer film made of polymethyl methacrylate, liquid crystal polyester, acetyl cellulose, saponified ethylene-vinyl acetate copolymer, polyvinyl chloride, etc. by about 1.0 to 6 times It is done. Among them, a polymer film obtained by uniaxially or biaxially stretching a polycarbonate film or a cyclic polyolefin film is preferable. Although there exist what is called a uniaxial phase difference film, a wide viewing angle phase difference film, a low photoelasticity phase difference film, etc., it is applicable to all.

  Moreover, the film which expressed optical anisotropy by application | coating and orientation of a liquid crystalline compound, and the film which expressed optical anisotropy by application | coating of an inorganic layered compound can also be used as retardation film. Such retardation films include what are called temperature-compensated retardation films, and films with a twisted orientation of rod-like liquid crystals sold under the trade name “LC film” by Nippon Oil Corporation. Also, a film with a tilted orientation of a rod-shaped liquid crystal sold under the trade name “NH film” by Shin Nippon Oil Co., Ltd., and a disk-shaped liquid crystal sold under the trade name “WV film” by FUJIFILM Corporation. Is a film with a tilt orientation, a fully biaxially oriented film sold under the trade name “VAC film” by Sumitomo Chemical Co., Ltd., and also sold under the trade name “new VAC film” by Sumitomo Chemical Co., Ltd. There are biaxially oriented films.

  Further, those obtained by attaching a protective film to these optical films can also be used as the optical film. As the protective film, a transparent resin film is used, and as the transparent resin, for example, an acetyl cellulose resin typified by triacetyl cellulose or diacetyl cellulose, a methacrylic resin typified by polymethyl methacrylate, a polyester resin, or a polyolefin Resin, polycarbonate resin, polyether ether ketone resin, polysulfone resin and the like. The resin constituting the protective film may contain an ultraviolet absorber such as a salicylic acid ester compound, a benzophenone compound, a benzotriazole compound, a triazine compound, a cyanoacrylate compound, or a nickel complex compound. As the protective film, an acetyl cellulose resin film such as a triacetyl cellulose film is preferably used.

  Among the optical films described above, the linear polarizing plate is often used in a state in which a protective film is attached to one or both sides of a polarizing film constituting the polarizing film, for example, a polarizing film made of a polyvinyl alcohol-based resin. . Moreover, although the above-mentioned elliptically polarizing plate is a laminate of a linearly polarizing plate and a retardation film, the linearly polarizing plate is often in a state where a protective film is attached to one side or both sides of the polarizing film. . When bonding the adhesive sheet by this invention to such an elliptically polarizing plate, it is normally bonded by the phase difference film side.

  In the optical film with an adhesive, it is preferable that a release film having been subjected to a release treatment as described above is attached to the surface of the adhesive layer to protect the surface of the adhesive layer until use. An optical film with an adhesive provided with a release film in this way is formed, for example, by applying the above-mentioned adhesive composition to the release treatment surface of the release film to form an adhesive sheet, A method of laminating on an optical film, a method of applying a pressure-sensitive adhesive composition on an optical film to form a pressure-sensitive adhesive sheet, attaching a release film to the surface of the pressure-sensitive adhesive to protect it, and making an optical film with a pressure-sensitive adhesive Can be manufactured.

  The thickness of the pressure-sensitive adhesive layer formed on the optical film is not particularly limited, but is usually preferably 30 μm or less, more preferably 10 μm or more, and further preferably 15 to 25 μm. When the thickness of the pressure-sensitive adhesive layer is 30 μm or less, the adhesiveness under high temperature and high humidity is improved, and the possibility of occurrence of floating or peeling between the glass substrate and the pressure-sensitive adhesive layer tends to be reduced. Moreover, it is preferable because reworkability tends to be improved, and if the thickness is 10 μm or more, the adhesive layer follows the dimensional change even if the dimension of the optical film bonded thereto changes. Since it fluctuates, there is no difference between the brightness at the peripheral edge of the liquid crystal cell and the brightness at the center, and this is preferable because white spots and color unevenness tend to be suppressed.

  After the optical film with the pressure-sensitive adhesive of the present invention is attached to a glass substrate to form an optical laminate, the pressure-sensitive adhesive layer is accompanied by the optical film when there is some defect and the optical film is peeled off from the glass substrate. Since the surface of the glass substrate that has been peeled off and is in contact with the pressure-sensitive adhesive layer hardly causes fogging or adhesive residue, it is easy to re-attach the optical film with the pressure-sensitive adhesive again to the glass substrate after peeling. That is, it is excellent in so-called reworkability.

[Optical laminate]
The optical film with the pressure-sensitive adhesive of the present invention can be made into an optical laminate by laminating the pressure-sensitive adhesive layer side on a glass substrate. In order to laminate an optical film with an adhesive on a glass substrate to form an optical laminate, for example, the release film is peeled off from the optical film with an adhesive obtained as described above, and the exposed adhesive layer surface is the surface of the glass substrate. You just have to stick together. As a glass substrate, the glass substrate of a liquid crystal cell, the glass for glare-proof, the glass for sunglasses etc. can be mentioned, for example. Among them, an optical film with an adhesive (upper polarizing plate) is laminated on the glass substrate on the front side (viewing side) of the liquid crystal cell, and another optical film with adhesive (lower polarizing plate) on the glass substrate on the back side of the liquid crystal cell. ) Is preferable because it can be used as a panel (liquid crystal panel) for a liquid crystal display device. Examples of the material of the glass substrate include soda lime glass, low alkali glass, non-alkali glass, and the like, and non-alkali glass is suitably used for the liquid crystal cell.

  Examples of some suitable layer configurations of the optical laminate according to the present invention are shown in cross-sectional schematic views in FIG. In the example shown in FIG. 1 (A), a polarizing film 5 is configured by sticking a protective film 3 having a surface treatment layer 2 on one surface of a polarizing film 1 on the surface opposite to the surface treatment layer 2. ing. In this example, the polarizing plate 5 is also the optical film 10 referred to in the present invention. An adhesive layer 20 is provided on the surface of the polarizing film 1 opposite to the protective film 3 to form an optical film 25 with an adhesive. And the surface on the opposite side to the polarizing plate 5 of the adhesive layer 20 is bonded to the liquid crystal cell 30 which is a glass substrate, and the optical laminated body 40 is comprised.

  In the example shown in FIG. 1B, the first protective film 3 having the surface treatment layer 2 is attached to one surface of the polarizing film 1 on the surface opposite to the surface treatment layer 2. On the other surface, a second protective film 4 is stuck to form a polarizing plate 5. Also in this example, the polarizing plate 5 is simultaneously the optical film 10 referred to in the present invention. An adhesive layer 20 is provided on the outer side of the second protective film 4 constituting the polarizing plate 5 to form an optical film 25 with an adhesive. And the surface on the opposite side to the polarizing plate 5 of the adhesive layer 20 is bonded to the liquid crystal cell 30 which is a glass substrate, and the optical laminated body 40 is comprised.

  In the example shown in FIG. 1 (C), a polarizing film 5 is formed by sticking a protective film 3 having a surface treatment layer 2 on one side of a polarizing film 1 on the surface opposite to the surface treatment layer 2. Yes. On the surface of the polarizing film 1 opposite to the protective film 3, a retardation film 7 is stuck via an interlayer adhesive 8 to constitute an optical film 10. An adhesive layer 20 is provided on the outer side of the retardation film 7 constituting the optical film 10 to constitute an optical film 25 with an adhesive. And the surface on the opposite side to the optical film 10 of the adhesive layer 20 is bonded to the liquid crystal cell 30 which is a glass substrate, and the optical laminated body 40 is comprised.

  In the example shown in FIG. 1 (D), the first protective film 3 having the surface treatment layer 2 is attached to one surface of the polarizing film 1 on the surface opposite to the surface treatment layer 2, and the polarizing film A polarizing plate 5 is configured by sticking a second protective film 4 to the other surface of 1. On the outer side of the second protective film 4 constituting the polarizing plate 5, a retardation film 7 is stuck via an interlayer adhesive 8 to constitute an optical film 10. An adhesive layer 20 is provided on the outer side of the retardation film 7 constituting the optical film 10 to constitute an optical film 25 with an adhesive. And the surface on the opposite side to the optical film 10 of the adhesive layer 20 is bonded to the liquid crystal cell 30 which is a glass substrate, and the optical laminated body 40 is comprised.

  In these examples, the first protective film 3 and the second protective film 4 are generally composed of a triacetyl cellulose film, but may be composed of the various transparent resin films described above. it can. The surface treatment layer formed on the surface of the first protective film 3 can be a hard coat layer, an antiglare layer, an antireflection layer, an antistatic layer, or the like. Of these, a plurality of layers may be provided.

  As shown in FIGS. 1C and 1D, when the retardation film 7 is laminated on the polarizing plate 5, a suitable example of the retardation film 7 is a medium-to-small liquid crystal display device. And a quarter-wave plate. In this case, it is general that the absorption axis of the polarizing plate 5 and the slow axis of the retardation film 7 which is a quarter wavelength plate are arranged so as to intersect at about 45 degrees. Depending on the characteristics, the angle may be shifted from 45 degrees to some extent. On the other hand, in the case of a large liquid crystal display device such as a television, a retardation film having various retardation values in accordance with the characteristics of the liquid crystal cell 30 is used for the purpose of phase difference compensation and viewing angle compensation of the liquid crystal cell 30. . In this case, the polarizing plate 5 and the retardation film 7 are generally arranged so that the absorption axis and the slow axis of the retardation film 7 are substantially orthogonal or substantially parallel. When the retardation film 7 is composed of a quarter wavelength plate, a uniaxial or biaxial stretched film is preferably used. When the retardation film 7 is provided for the purpose of retardation compensation or viewing angle compensation of the liquid crystal cell 30, in addition to the uniaxial or biaxially stretched film, it is also oriented in the thickness direction in addition to the uniaxial or biaxially stretched film. What is called an optical compensation film, such as a film or a film obtained by coating and fixing a retardation-expressing substance such as liquid crystal on a support film, can also be used as the retardation film 7.

  Similarly, when the polarizing plate 5 and the retardation film 7 are bonded via the interlayer adhesive 8 as in the example shown in FIGS. 1C and 1D, the interlayer adhesive 8 includes A typical acrylic pressure-sensitive adhesive is usually used, but it is of course possible to use a pressure-sensitive adhesive sheet as defined herein. In the case where the absorption axis of the polarizing plate 5 and the slow axis of the retardation film 7 are arranged so as to be substantially orthogonal or substantially parallel like the large liquid crystal display device described above, In applications where the phase difference film 7 can be roll-to-roll-bonded and re-peelability between the two is not required, the interlayer adhesive 8 shown in (C) and (D) of FIG. It is also possible to use an adhesive that can be firmly bonded once bonded and cannot be peeled off. Examples of such an adhesive include an aqueous adhesive that is composed of an aqueous solution or an aqueous dispersion, and develops an adhesive force by evaporating water as a solvent, an ultraviolet curing that cures by ultraviolet irradiation and develops an adhesive force. Examples thereof include a mold adhesive.

  1 (C) and (D) shown in FIG. 1 can also be distributed by themselves, in which the pressure-sensitive adhesive layer 20 is formed on the retardation film 7. Can be a film. An optical film with an adhesive with an adhesive layer formed on a retardation film can be bonded to a liquid crystal cell that is a glass substrate to form an optical laminate, and a polarizing plate is provided on the retardation film side. It can also paste and can be set as another optical film with an adhesive.

  FIG. 1 shows an example in which the optical film 25 with an adhesive is arranged on the viewing side of the liquid crystal cell 30, but the optical film with an adhesive according to the present invention is the back side of the liquid crystal cell, that is, the back. It can also be placed on the light side. When the optical film with pressure-sensitive adhesive of the present invention is disposed on the back side of the liquid crystal cell, a protective film having no surface treatment layer is employed instead of the protective film 3 having the surface treatment layer 2 shown in FIG. Others can be configured similarly to (A) to (D) of FIG. In this case, various optical films known to be disposed on the back side of the liquid crystal cell, such as a brightness enhancement film, a light collecting film, and a diffusion film, may be provided outside the protective film constituting the polarizing plate. Is possible.

  As described above, the optical layered body of the present invention can be suitably used for a liquid crystal display device. The liquid crystal display device formed from the optical laminated body of the present invention includes, for example, a notebook type, a desktop type, a personal computer liquid crystal display including a PDA (Personal Digital Assistant), a television, an in-vehicle display, an electronic dictionary, and a digital camera. It can be used for digital video cameras, electronic desk calculators, watches, etc.

  EXAMPLES Hereinafter, although an Example is given and this invention is demonstrated further more concretely, this invention is not limited by these examples. In the examples, “%” and “part” representing the amount used or content are based on weight unless otherwise specified.

In the following examples, the weight average molecular weight is 4 columns of “TSKgel XL” manufactured by Tosoh Corporation as a column in the GPC device, and “Shodex GPC KF sold by Showa Denko K.K.
-802 ”, 5 in total, connected in series, tetrahydrofuran as eluent, sample concentration 5 mg / mL, sample introduction amount 100 μL, temperature 40 ° C., flow rate 1 mL / min, standard It is the value measured by polystyrene conversion.

  First, the polymerization example which manufactured the acrylic resin (A) prescribed | regulated by this invention used as the main component of an adhesive composition, and the acrylic resin similar to it but remove | deviated from the prescription | regulation of this invention is shown. In the following polymerization examples, the following were used as the carboxyl group-containing monomer.

β-CEA: β-carboxyethyl acrylate sold by Daicel Cytec Co., Ltd. under the trade name “β-CEA”. Its chemical composition is
CH ₂ = CH (COOCH ₂ CH ₂ ) _n COOH (n = average 1)
Specifically, 2-carboxyethyl acrylate (namely, dimer of acrylic acid) 40%, oligomer of acrylic acid trimer or higher 40%, and acrylic acid 20%. Hereinafter, “β-CEA” is displayed following the product name. In the following description, “2-carboxyethyl acrylate” refers to a dimer of acrylic acid, that is, CH ₂ ═CHCOOCH ₂ CH ₂ COOH.
It shall refer to itself.

[Polymerization Example 1]
A reactor equipped with a cooling pipe, nitrogen introduction pipe, thermometer and stirrer was charged with 120 parts of ethyl acetate, the air inside the apparatus was replaced with nitrogen gas, and the internal temperature was raised to 75 ° C. without oxygen. It was. Azobisisobutyronitrile (polymerization initiator) As a monomer (A-1), the total amount of 0.05 part dissolved in 5 parts of ethyl acetate was added, and the internal temperature was kept at 74 to 76 ° C. 69.9 parts of butyl acrylate, 20.0 parts of methyl acrylate and 8.0 parts of 2- (2-phenoxyethoxy) ethyl acrylate, 2-hydroxyethyl acrylate 2.0 as the monomer (A-2) And a mixed solution of 0.1 part of β-CEA as a monomer (A-3) was dropped into the reaction system over 2 hours. Thereafter, the temperature was kept at 74 to 76 ° C. for 5 hours to complete the reaction. Finally, ethyl acetate was added to adjust the concentration of the acrylic resin to 40% to prepare an acrylic resin ethyl acetate solution. The obtained acrylic resin had a polystyrene equivalent weight average molecular weight Mw by GPC of 680,000 and Mw / Mn of 4.9. This is designated as acrylic resin A.

[Polymerization Example 2]
In a reaction vessel equipped with a cooling tube, a nitrogen introduction tube, a thermometer and a stirrer, 81.8 parts of ethyl acetate, 69.7 parts of butyl acrylate as monomer (A-1), 20.0 parts of methyl acrylate and 8.0 parts of 2- (2-phenoxyethoxy) ethyl acrylate, 2.0 parts of 2-hydroxyethyl acrylate as monomer (A-2), and .beta.-CEA as monomer (A-3). The internal temperature was raised to 55 ° C. while charging 3 parts and replacing the air in the apparatus with nitrogen gas so as not to contain oxygen. Thereafter, a total amount of a solution prepared by dissolving 0.14 parts of azobisisobutyronitrile (polymerization initiator) in 10 parts of ethyl acetate was added. One hour after the addition of the initiator, this temperature is maintained, and then, while maintaining the internal temperature at 54 to 56 ° C., ethyl acetate is continuously added into the reaction vessel at an addition rate of 17.3 parts / hr. When the concentration of the solution reached 35%, the addition of ethyl acetate was stopped, and the mixture was kept at this temperature until 12 hours had passed since the start of the addition of ethyl acetate. Finally, ethyl acetate was added to adjust the concentration of the acrylic resin to 20% to prepare an acrylic resin ethyl acetate solution. The obtained acrylic resin had a polystyrene-reduced weight average molecular weight Mw by GPC of 153,000 and Mw / Mn of 4.2. This is designated as acrylic resin B.

[Polymerization Example 3]
The amount of butyl acrylate was changed to 68.85 parts, the amount of 2-hydroxyethyl acrylate was changed to 3.0 parts, and the amount of β-CEA was changed to 0.15 parts. In the same manner as in 2, an acrylic resin ethyl acetate solution was prepared. The resulting acrylic resin had a polystyrene equivalent weight average molecular weight Mw of 1,440,000 and Mw / Mn of 4.6 by GPC. This is designated as acrylic resin C.

[Polymerization Example 4]
The amount of butyl acrylate was changed to 67.9 parts, the amount of 2-hydroxyethyl acrylate was changed to 4.0 parts, and the amount of β-CEA was changed to 0.1 parts. In the same manner as in 2, an acrylic resin ethyl acetate solution was prepared. The obtained acrylic resin had a polystyrene equivalent weight average molecular weight Mw of 1,470,000 and Mw / Mn of 4.5 by GPC. This is designated as acrylic resin D.

[Polymerization Example 5]
The amount of butyl acrylate charged was changed to 70.4 parts, the amount of 2-hydroxyethyl acrylate charged was changed to 1.0 parts, β-CEA was not charged, and 0.6 parts of acrylic acid was charged instead. Except for the above, an acrylic resin ethyl acetate solution was prepared in the same manner as in Polymerization Example 1. The obtained acrylic resin had a polystyrene equivalent weight average molecular weight Mw of 630,000 and Mw / Mn of 5.0 by GPC. This is referred to as an acrylic resin X.

  Table 1 summarizes the charge composition of the monomers in the above Polymerization Examples 1 to 5, and the weight average molecular weight and Mw / Mn of the resulting acrylic resin. In Polymerization Example 1, the amount of β-CEA charged is 0.1% based on the total amount of monomers (that is, the resulting acrylic resin) as shown in Table 1, but in β-CEA Since 2-carboxyethyl acrylate contained is 40% as described above, the proportion of structural units derived from 2-carboxyethyl acrylate in the acrylic resin is 0.04%. The polymerization examples 2 to 4 also follow this.

(Footnotes in Table 1: Meaning of symbols representing monomers)
(A-1)
BA: butyl acrylate MA: methyl acrylate PEA2: 2- (2-phenoxyethoxy) ethyl acrylate (A-2)
2HEA: 2-hydroxyethyl acrylate (A-3)
β-CEA: 2-carboxyethyl acrylate (dimer of acrylic acid) 40%,
A mixture of 40% oligomer of acrylic acid trimer or higher and 20% acrylic acid AA: Acrylic acid

  Next, examples and comparative examples in which pressure-sensitive adhesives were prepared using the acrylic resin produced above and applied to optical films are shown. In the following examples, the following were used as the crosslinking agent, organic acid, and silane compound, respectively. “Coronate L” and “KBM-403” are trade names.

<Crosslinking agent>
Coronate L: Trimethylolpropane adduct of tolylene diisocyanate in ethyl acetate solution (solid content: 75%), obtained from Nippon Polyurethane Co., Ltd.

<Organic acid>
Acrylic acid: CH ₂ = CHCOOH, liquid, obtained from Nippon Shokubai Co., Ltd.

<Silane compounds>
KBM-403: 3-glycidoxypropyltrimethoxysilane, liquid, obtained from Shin-Etsu Chemical Co., Ltd.

[Examples 1 to 11 and Comparative Examples 1 to 5]
(A-1) Production of pressure-sensitive adhesive compositions 1 to 5 Using the 40% ethyl acetate solution of acrylic resin A obtained in Polymerization Example 1, with respect to 100 parts of the solid content, the above-mentioned crosslinking agent (Coronate L), Each amount of organic acid (acrylic acid) shown in Table 2 and 0.5 part of the above-mentioned silane compound (KBM-403) are mixed, and ethyl acetate is added so that the solid content concentration becomes 28%. Thus, pressure-sensitive adhesive compositions 1 to 5 were prepared. In addition, although the crosslinking agent (Coronate L) is an ethyl acetate solution having a solid content concentration of 75% as described above, the addition amount shown in Table 2 is the solid content amount.

(A-2) Production of pressure-sensitive adhesive compositions 6 and 7 A pressure-sensitive adhesive composition was prepared by performing the same operation as in (a-1) except that the 20% ethyl acetate solution of acrylic resin B obtained in Polymerization Example 2 was used. 6 and 7 were prepared.

(A-3) Production of pressure-sensitive adhesive compositions 8 and 9 A pressure-sensitive adhesive composition was prepared by performing the same operation as in (a-1) except that the 20% ethyl acetate solution of acrylic resin C obtained in Polymerization Example 3 was used. 8 and 9 were prepared.

(A-4) Production of pressure-sensitive adhesive compositions 10 and 11 A pressure-sensitive adhesive composition was prepared by performing the same operation as in (a-1) except that the 20% ethyl acetate solution of acrylic resin D obtained in Polymerization Example 4 was used. 10 and 11 were prepared.

(A-5) Manufacture of adhesive composition 12-15 Except not having mixed the organic acid, operation similar to (a-1)-(a-4) was performed, respectively, and adhesive composition 12-15 was carried out. Prepared.

(A-6) Production of pressure-sensitive adhesive composition 16 An operation according to (a-1) was performed, except that a 40% ethyl acetate solution of acrylic resin X obtained in Polymerization Example 5 was used and no organic acid was mixed. Thus, an adhesive composition 16 was prepared.

(B) Evaluation of viscosity change of pressure-sensitive adhesive composition For each pressure-sensitive adhesive composition prepared in the above (a-1) to (a-6), the viscosity was determined by the method described above immediately after preparation and after 6 hours of preparation. Was measured. The value immediately after the preparation is shown in the column “η ₁ ” in Table 2, the value 6 hours after the preparation is shown in the column “η ₂ ” in Table 2, and calculated as (η ₂ −η ₁ ) / η ₁ × 100. The change rate of the viscosity is shown in the column of “Viscosity change” in Table 2.

(C) Preparation of pressure-sensitive adhesive sheet Each of the pressure-sensitive adhesive compositions prepared in the above (a-1) to (a-6) was subjected to a release treatment on a polyethylene terephthalate film [trade name “PLR-382050”, Applicable to the mold release surface of the separator (obtained from Lintec Co., Ltd.) using an applicator so that the thickness after drying is 20 μm, and dried at 100 ° C. for 1 minute to produce an adhesive sheet did.

(D) Measurement of gel fraction of pressure-sensitive adhesive sheet The pressure-sensitive adhesive sheet prepared in (c) above was left at room temperature for 1 day, then left for 4 days, and after 8 days, respectively. The gel fraction was measured by the method. The value after leaving for 1 day is in the column “1st day” in Table 2, the value after being left for 4 days in the “4th day” column in Table 2, and the value after being left for 8 days in “2” in Table 2. The ratio of the gel fraction after standing for 1 day to the gel fraction after standing for 8 days is shown in the column of “Day 1” and “Day 8” in Table 2, respectively. The ratio of the gel fraction after standing for 4 days to the gel fraction was shown in the column of “Day 4/8” in Table 2.

(E) Production of polarizing plate with pressure-sensitive adhesive A polarizing film having iodine adsorbed and oriented on polyvinyl alcohol is sandwiched between protective films made of triacetyl cellulose on both sides of a polarizing film having a three-layer structure. ), The surface of the pressure-sensitive adhesive sheet opposite to the separator (pressure-sensitive adhesive surface) was pasted with a laminator, and then cured for 7 days at a temperature of 23 ° C. and a relative humidity of 65%. Produced.

(F) Production and Evaluation of Optical Laminate After separating the separator from the pressure-sensitive adhesive polarizing plate produced in (e) above, the pressure-sensitive adhesive surface was changed to a glass substrate for liquid crystal cells [trade name “EAGLE XG” from Corning Inc. It was pasted on both sides of [Acquisition] so as to be crossed Nicol, and an optical laminate was produced. This optical laminate was subjected to a heat resistance test that was stored for 96 hours under dry conditions at a temperature of 80 ° C. Thereafter, the appearance of white spots when light was incident from one polarizing film side was visually observed. The results were classified according to the following criteria, and are shown in the column “White Leak” in Table 2.

<Expression of white spots>
A: No white spots are observed.
○: White spots are hardly noticeable.
Δ: White spots are slightly noticeable.
X: White spots are noticeable.

  In addition, when the same optical laminate as above was subjected to a heat resistance test for 300 hours under dry conditions at a temperature of 80 ° C. (indicated as “heat resistance” in Table 2), it was stored at a temperature of 60 ° C. and a relative humidity of 90% for 300 hours. 1 cycle (1 hour) in the case where the heat and humidity resistance test is performed (indicated as “moisture and heat resistance” in Table 2) and when the temperature is lowered to −30 ° C. from the state heated to 70 ° C. and then raised to 70 ° C. ), When the heat shock resistance test was repeated 100 cycles (indicated as “HS resistance” in Table 2), the optical laminate after the test was visually observed. The results were classified according to the following criteria and summarized in the “Durability” column of Table 2.

<Evaluation criteria for heat resistance test, moist heat resistance test and heat shock resistance test>
A: No change in appearance such as floating, peeling or foaming is observed.
○: Almost no change in appearance such as floating, peeling or foaming.
Δ: Appearance changes such as floating, peeling and foaming are slightly noticeable.
X: Remarkable changes in appearance such as floating, peeling, foaming, etc.

(G) Reworkability evaluation of optical film with adhesive The reworkability was evaluated as follows. First, the polarizing plate with an adhesive produced in the above (e) was cut into a test piece having a size of 25 mm × 150 mm. Next, after peeling off the separator from this test piece, it was attached to the glass substrate for a liquid crystal cell on the pressure-sensitive adhesive layer side using a sticking apparatus [trade name “Lamipacker” manufactured by Fuji Plastics Co., Ltd.], temperature 50 ° C., pressure Autoclaving was carried out at 5 kg / cm ² (490.3 kPa) for 20 minutes. Subsequently, after heat treatment at 70 ° C. for 2 hours and subsequent storage in an oven at 50 ° C. for 48 hours, a polarizing plate is attached together with the pressure-sensitive adhesive layer from this sticking test piece in an atmosphere at a temperature of 23 ° C. and a relative humidity of 50%. The film was peeled off at a speed of 300 mm / min in the direction of 180 ° (in the direction parallel to the glass surface when the polarizing plate was peeled upside down), and the state of the glass plate surface was observed and classified according to the following criteria. The results are also shown in the column “Reworkability” in Table 2.

<Evaluation criteria for reworkability>
A: No fogging or the like is observed on the glass plate surface.
A: Almost no fogging or the like is observed on the glass plate surface.
(Triangle | delta): Cloudiness etc. are recognized by the glass plate surface.
X: The remainder of an adhesive is recognized by the glass plate surface.

(Footnote in Table 2)
Meaning of symbol representing functional group-containing monomer in column of “acrylic resin” 2HEA: 2-hydroxyethyl acrylate (hydroxyl group-containing component)
β-CEA: 2-carboxyethyl acrylate (dimer of acrylic acid) 40%,
40% oligomer of acrylic acid trimer or higher,
Mixture of 20% acrylic acid (carboxyl group-containing component)
AA: Description of the column of acrylic acid “viscosity” η ₁ : Viscosity immediately after preparation of the pressure-sensitive adhesive composition η ₂ : Viscosity 6 hours after preparation of the pressure-sensitive adhesive composition Viscosity change (%) = (η ₂ −η ₁ ) / η ₁ × 100

  As shown in Table 1 and Table 2, a predetermined amount of a crosslinking agent is blended in acrylic resin A in which a predetermined amount of 2-carboxyethyl acrylate corresponding to formula (II) is copolymerized, and a predetermined amount of organic acid is added. In Examples 1 to 11, which were mixed to constitute a pressure-sensitive adhesive composition, the first day and the fourth day with respect to the gel fraction on the 8th day after coating in a sheet shape while suppressing the viscosity change of the composition. An adhesive sheet having a high gel fraction ratio is provided. Therefore, it has excellent workability when it is coated in a sheet shape, and it can shorten the curing time until it can be processed without problems after coating. It becomes. In the pressure-sensitive adhesive sheets of these examples, almost satisfactory results were obtained in heat resistance, moist heat resistance and heat shock resistance.

  On the other hand, the acrylic resin has a structural unit derived from 2-carboxyethyl acrylate corresponding to the formula (II), but Comparative Examples 1 to 4 to which no organic acid is added have a viscosity change of the composition. Large and coatability is not sufficient. In Comparative Example 5 using the acrylic resin X having no structural unit derived from 2-carboxyethyl acrylate corresponding to the formula (II), the gel fraction on the 8th day after coating in a sheet form The ratio of the gel fraction on the first day to the ratio is much less than 0.8, and the ratio of the gel fraction on the fourth day is less than 0.97, so the processability is not sufficient.

  The pressure-sensitive adhesive composition of the present invention has a small change in viscosity over time and exhibits good coatability. In addition, the pressure-sensitive adhesive sheet obtained from this pressure-sensitive adhesive composition can shorten the curing time required until processing can be performed after forming the sheet, and has excellent workability and durability and rework. Excellent in properties. The optical film provided with the pressure-sensitive adhesive sheet is suitably used for a liquid crystal display device.

1 …… Polarizing film,
2 ... Surface treatment layer
3 ... (first) protective film,
4 …… Second protective film,
5 ... Polarizing plate,
7 ... retardation film,
8 …… Interlayer adhesive,
10 …… Optical film,
20 ... Adhesive layer (adhesive sheet) bonded to the liquid crystal cell (glass substrate),
25 …… Optical film with adhesive,
30 ... Liquid crystal cell (glass substrate),
40: Optical laminate.

Claims (12)

(A) (A-1) The following formula (I)

(In the formula, R ₁ represents a hydrogen atom or a methyl group; R ₂ represents an alkyl group or an aralkyl group having 14 or less carbon atoms, and the hydrogen atom constituting these groups is a group —O— (C ₂ H ₄ O) may be substituted with _n- R ₃ , where n represents 0 or an integer of 1 to 4, and R ₃ represents an alkyl group or aryl group having 12 or less carbon atoms)
(Meth) acrylic acid ester represented by 94.8 to 99.89% by weight,
(A-2) 0.1 to 5% by weight of a (meth) acrylic monomer having a hydroxyl group, and (A-3) the following formula (II)

(Wherein R ₄ represents a hydrogen atom or a methyl group; A represents a divalent organic group having 2 to 4 carbon atoms)
0.01 to 0.2% by weight of a carboxyl group-containing (meth) acrylic acid ester represented by
100 parts by weight of an acrylic resin having a weight average molecular weight of 500,000 to 2,000,000,
(B) 0.01-5 parts by weight of a crosslinking agent containing an isocyanate compound, and (C) the following formula (III)

(Wherein R ₅ represents a hydrogen atom or an alkyl or alkenyl group having 4 or less carbon atoms)
A pressure-sensitive adhesive composition comprising 0.03 to 5 parts by weight of a carboxylic acid represented by the formula: The pressure-sensitive adhesive composition according to claim 1, wherein the carboxyl group-containing (meth) acrylic acid ester (A-3) is 2-carboxyethyl acrylate. Furthermore, the pressure-sensitive adhesive composition according to any one of claims 1 to 2 containing (D) silane compound 0.03 to 2 parts by weight. It forms in the sheet form from the adhesive composition in any one of Claims 1-3 , The adhesive sheet characterized by the above-mentioned. The pressure-sensitive adhesive according to claim 4 , wherein the ratio of the gel fraction after 1 day from the application to the gel fraction after 8 days from the application of the pressure-sensitive adhesive composition into a sheet is 0.8 or more. Agent sheet. The pressure-sensitive adhesive according to claim 4 , wherein the ratio of the gel fraction after 4 days after the application to the gel fraction after 8 days from the application of the pressure-sensitive adhesive composition into a sheet is 0.97 or more. Agent sheet. The pressure-sensitive adhesive sheet according to any one of claims 4 to 6 , which is formed on a plastic film. The pressure-sensitive adhesive sheet according to claim 7 , wherein the plastic film is a release film subjected to a release treatment. An optical film with an adhesive, wherein the adhesive sheet according to any one of claims 4 to 6 is bonded to an optical film. The optical film with an adhesive according to claim 9 , wherein the optical film is selected from a polarizing plate and a retardation film. An optical laminated body, wherein the optical film with an adhesive according to claim 9 or 10 is laminated on a glass substrate on the adhesive sheet side. A method for producing a pressure-sensitive adhesive sheet according to claim 1, wherein the pressure-sensitive adhesive composition further comprises a solvent, and the solvent is dried and removed.

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