JP2005325340A - Adhesive composition, adhesive layer and method for producing the same - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide an adhesive composition having improved coatability and keeping the durability without particularly increasing the amount of solvent in coating, an adhesive layer produced by using the composition and a method for producing the composition, etc. <P>SOLUTION: The adhesive composition contains an acrylic polymer containing ≥60 wt.% alkyl acrylate having a 1-9C alkyl group as a monomer unit, having a weight-average molecular weight of ≥1,500,000 and containing ≥20 wt.% component having a molecular weight of ≤100,000, and an organic solvent. The composition contains a poor solvent having a solubility parameter (SP value) δ2 [(J/cm<SP>3</SP>)<SP>1/2</SP>] satisfying the formula: +1.7≤Δδ(=δ1-δ2)≤+5 wherein δ1 [(J/cm<SP>3</SP>)<SP>1/2</SP>] is the solubility parameter (SP value) of the homopolymer of the monomer constituting the main part of the acrylic polymer. The amount of the poor solvent is 20-60 wt.% of the total organic solvent. <P>COPYRIGHT: (C)2006,JPO&NCIPI

Description

  The present invention relates to a solvent-type acrylic pressure-sensitive adhesive composition, a pressure-sensitive adhesive layer formed using the same, a manufacturing method thereof, an optical member formed with the pressure-sensitive adhesive layer, and an image display device using the same. . The present invention is a pressure-sensitive adhesive optical member such as a polarizing plate, a retardation plate, an optical compensation film, a brightness enhancement film, and a laminate thereof, a liquid crystal display device using the pressure-sensitive optical member, an organic EL display device, a PDP, and the like. This is useful as a technique related to the image display apparatus.

  The pressure-sensitive adhesive layer used for optics is required to have a high level of thickness and surface uniformity, and it is applied at a low concentration so that the viscosity of the polymer solution is low in order to improve coating properties. ing. However, in recent years, in reality, it is desirable to reduce the use of organic solvents as much as possible in consideration of the environment.

  In addition, as adhesives that do not use organic solvents, emulsion adhesives that use aqueous dispersion media and UV polymerization type adhesives that do not contain solvents are known. However, such as water resistance problems and thickness uniformity, It is not yet ready for use.

  On the other hand, as a device for preventing the viscosity of the polymer solution from increasing even when the polymer concentration is increased, there is a method of reducing the molecular weight of the polymer. However, optical members used in liquid crystal display devices and the like, such as polarizing plates and retardation plates, are attached to liquid crystal cells via an adhesive, and the expansion and contraction of optical members is large under heating and humidification conditions. After sticking, there is a tendency to float or peel off. For this reason, the pressure-sensitive adhesive for optical members is required to have durability that can be applied under heating conditions and humidification conditions, and it is difficult to lower the molecular weight. For example, Patent Document 1 discloses that when an acrylic polymer is used as an optical pressure-sensitive adhesive, the polymer component having a weight average molecular weight of 100,000 or less is made 15% by weight or less.

  In addition, in Patent Document 2, a vinyl chloride resin poor solvent and a good solvent are used in combination in the organosol when the second layer sheet is applied to the first layer sheet with respect to the production method of the vinyl chloride resin laminated sheet. Is described. However, this laminated sheet corresponds to the base material of the pressure-sensitive adhesive sheet, and uses a good solvent to improve the adhesion at the interface, and there is no disclosure regarding the formation of the pressure-sensitive adhesive layer.

JP-A 64-66283 Japanese Patent Laid-Open No. 11-157019

  Accordingly, an object of the present invention is to provide a pressure-sensitive adhesive composition that can improve coating properties and maintain durability without particularly increasing the amount of solvent during coating, and a pressure-sensitive adhesive formed using the same. It is in providing an agent layer and its manufacturing method. Furthermore, the objective of this invention is providing the adhesive optical member in which the said adhesive layer was formed, and an image display apparatus using the same.

  In order to achieve the above object, the inventors of the present invention focused on the viscosity of the pressure-sensitive adhesive solution and conducted extensive research on its reduction method. This can be achieved by adding an appropriate amount of a specific poor solvent to the polymer component. As a result, the present invention has been completed.

That is, the pressure-sensitive adhesive composition of the present invention contains 60% by weight or more of an acrylic acid alkyl ester having an alkyl group having 1 to 9 carbon atoms as a monomer unit, and has a weight average molecular weight of 1.5 million or more and a molecular weight of 100,000 or less. In the pressure-sensitive adhesive composition containing an acrylic polymer having a component ratio of 20% by weight or less and an organic solvent, the solubility parameter (SP value) of the homopolymer of the main monomer unit constituting the acrylic polymer is δ1 “(J / Cm ³ ) ^1/2 ”, the solubility parameter (SP value) δ2 [(J /) so that the solubility parameter (SP value) difference (Δδ = δ1-δ2) is +1.7 to +5 cm ³ ) ^1/2 ] is contained in an amount of 20 to 60% by weight of the total amount of the organic solvent.

  According to the pressure-sensitive adhesive composition of the present invention, a poor solvent having a moderate solubility parameter is used based on the solubility parameter of the homopolymer of the main monomer unit constituting the acrylic polymer, and an appropriate amount thereof is used. Therefore, the spread of the molecular chain can be made sufficiently small without precipitating the acrylic polymer, and the coating property can be improved by reducing the viscosity without particularly increasing the amount of the solvent during coating. At that time, since the weight average molecular weight of the acrylic polymer is sufficiently increased and the low molecular weight component is reduced, the durability of the resulting pressure-sensitive adhesive layer can be maintained, and the crosslinkability of the acrylic polymer is improved.

  In the above, it is preferable that the acrylic polymer contains 0.2 to 7% by weight of an unsaturated carboxylic acid as a monomer unit. By copolymerizing an appropriate amount of such an unsaturated carboxylic acid, the adhesive force to the liquid crystal cell can be controlled to some extent while maintaining durability even when the molecular chain of the acrylic polymer is small. .

  Moreover, it is preferable that solid content concentration is 10 to 30 weight%. The pressure-sensitive adhesive composition of the present invention can improve the coating property more reliably without particularly increasing the amount of the solvent within such a solid content concentration range.

  On the other hand, the pressure-sensitive adhesive layer of the present invention is a pressure-sensitive adhesive layer obtained by coating and drying the pressure-sensitive adhesive composition as described above, and a silane coupling agent is added to 100 parts by weight of the acrylic polymer. 0.01 to 1 part by weight, 0.01 to 5 parts by weight of a crosslinking agent is contained, and the gel fraction after crosslinking is 45 to 95% by weight. According to the pressure-sensitive adhesive layer of the present invention, in addition to the above-described operational effects and durability maintaining effect, the addition of a suitable amount of the silane coupling agent improves the adhesion to the adherend, and By adding an appropriate amount of a crosslinking agent, it is possible to prevent adhesive residue at the time of peeling and improve durability.

  Moreover, the manufacturing method of the adhesive layer of this invention is characterized by including the process of applying the adhesive composition in any one of the said, and the process of drying a coated material. According to the production method of the present invention, due to the above-described effects, the coating property can be improved by reducing the viscosity without particularly increasing the amount of solvent during coating. Moreover, since durability of the obtained adhesive layer is maintained, it becomes a highly durable thing.

  On the other hand, the pressure-sensitive adhesive optical member of the present invention is characterized in that the pressure-sensitive adhesive layer is formed on one side or both sides of the optical member. Moreover, the image display apparatus of the present invention uses at least one adhesive optical member. For this reason, by the above-described effects of the pressure-sensitive adhesive layer of the present invention, the coating property can be improved and the durability can be maintained without particularly increasing the amount of solvent during coating.

  The pressure-sensitive adhesive composition of the present invention includes an acrylic polymer containing 60% by weight or more of an acrylic acid alkyl ester as a monomer unit, and the acrylic polymer has a weight average molecular weight of 1.5 million or more and a molecular weight of 100,000 or less. Is 20% by weight or less.

  The acrylic acid alkyl ester serving as the monomer unit of the acrylic polymer is preferably an alkyl alkyl ester having an alkyl group having 1 to 9, preferably 2 to 6, more preferably 3 to 4 carbon atoms. Either can be used.

  The acrylic polymer is preferably copolymerized with 60 wt% or more, more preferably 70 wt% or more of such an acrylic acid alkyl ester from the viewpoint of adhesive properties. Examples of the alkyl acrylate having an alkyl group having 1 to 9 carbon atoms include methyl acrylate, ethyl acrylate, propyl acrylate, n-butyl acrylate, s-butyl acrylate, t-butyl acrylate, isobutyl acrylate, hexyl acrylate, and 2-ethylhexyl acrylate. , N-octyl acrylate, isooctyl acrylate, n-nonyl acrylate and the like. These may be used individually by 1 type and may use 2 or more types together.

  The acrylic polymer preferably contains 0.2 to 7% by weight, more preferably 0.5 to 5% by weight, of unsaturated carboxylic acid as a monomer unit. If the content of the unsaturated carboxylic acid exceeds 7% by weight, the adhesive force to the liquid crystal cell becomes too large or too hard, which is not preferable. On the other hand, if it is less than 0.2% by weight, the durability is adversely affected.

  Examples of the unsaturated carboxylic acid include acrylic acid, methacrylic acid, carboxyethyl (meth) acrylate, carboxypentyl (meth) acrylate, itaconic acid, maleic acid, fumaric acid, and crotonic acid. These anhydrides can also be used. Of these, acrylic acid and methacrylic acid are particularly preferably used. These compounds may be used alone or in combination of two or more.

  The acrylic polymer can further contain another monomer such as a hydroxyl group-containing monomer as a monomer unit. Other monomers include alkyl methacrylates having 1 to 4 carbon atoms such as methyl methacrylate, ethyl methacrylate, butyl methacrylate; 2-hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate, hydroxy Monomers having a hydroxyl group such as butyl (meth) acrylate, hydroxyhexyl (meth) acrylate, N-methylol (meth) acrylamide; monomers containing an epoxy group such as glycidyl (meth) acrylate; (meth) acrylamide, N, N-dimethyl (Meth) acrylamide, N, N-diethyl (meth) acrylamide, (meth) acryloylmorpholine, (meth) acetonitrile, vinylpyrrolidone, N-cyclohexylmaleimide, itaconimide, N, N Monomers having N elements of dimethylaminoethyl (meth) acrylamide and the like. Furthermore, a child using vinyl acetate, styrene or the like can be used. These monomers can be used alone or in combination of two or more.

  The other polymerizable monomers other than the above-mentioned alkyl (meth) acrylate and unsaturated carboxylic acid include a polymerizable monomer for adjusting the glass transition point and peelability of the (meth) acrylic polymer. It can be used as long as the effect is not impaired.

  Examples of other polymerizable monomers used in the (meth) acrylic polymer of the present invention include aggregation of sulfonic acid group-containing monomers, phosphoric acid group-containing monomers, cyano group-containing monomers, vinyl ester monomers, aromatic vinyl monomers, and the like. Works as an adhesive strength improver and a crosslinking base point for components that improve strength and heat resistance, hydroxyl group-containing monomers, amide group-containing monomers, amino group-containing monomers, imide group-containing monomers, epoxy group-containing monomers, N-acryloylmorpholine, vinyl ether monomers, etc. A component having a functional group can be used as appropriate. Furthermore, alkyl (meth) acrylate having an alkyl group having 10 or more carbon atoms can be used as appropriate. These monomer compounds may be used alone or in admixture of two or more.

  Examples of the sulfonic acid group-containing monomer include styrene sulfonic acid, allyl sulfonic acid, 2- (meth) acrylamide-2-methylpropane sulfonic acid, (meth) acrylamide propane sulfonic acid, sulfopropyl (meth) acrylate, (meth And acryloyloxynaphthalene sulfonic acid.

  Examples of the phosphoric acid group-containing monomer include 2-hydroxyethylacryloyl phosphate.

  Examples of the cyano group-containing monomer include acrylonitrile and methacrylonitrile.

  Examples of the vinyl ester monomer include vinyl acetate, vinyl propionate, vinyl laurate, vinyl pyrrolidone, and the like.

  Examples of the aromatic vinyl monomer include styrene, chlorostyrene, chloromethyl styrene, α-methyl styrene, and the like.

  Examples of the hydroxyl group-containing monomer include 2-hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate, 3-hydroxypropyl (meth) acrylate, 4-hydroxybutyl (meth) acrylate, 6-hydroxyhexyl ( (Meth) acrylate, 8-hydroxyoctyl (meth) acrylate, 10-hydroxydecyl (meth) acrylate, 12-hydroxylauryl (meth) acrylate, (4-hydroxymethylcyclohexyl) methyl acrylate, N-methylol (meth) acrylamide N-hydroxy (meth) acrylamide, vinyl alcohol, allyl alcohol, 2-hydroxyethyl vinyl ether, 4-hydroxybutyl vinyl ether, diethylene glycol monovinyl ether Tell, and the like.

  Examples of amide group-containing monomers include acrylamide, methacrylamide, diethyl acrylamide, N-vinyl pyrrolidone, N, N-dimethyl acrylamide, N, N-dimethyl methacrylamide, N, N-diethyl acrylamide, N, N-diethyl methacryl. Examples include amide, N, N′-methylenebisacrylamide, N, N-dimethylaminopropylacrylamide, N, N-dimethylaminopropylmethacrylamide, N- (meth) acryloylmorpholine, and the like.

  Examples of the amino group-containing monomer include N, N-dimethylaminoethyl (meth) acrylate, N, N-dimethylaminopropyl (meth) acrylate, N- (meth) acryloylmorpholine, and (meth) acrylic acid aminoalkyl ester. Etc.

  Examples of the imide group-containing monomer include cyclohexylmaleimide, isopropylmaleimide, N-cyclohexylmaleimide, and itaconimide.

  Examples of the epoxy group-containing monomer include glycidyl (meth) acrylate and allyl glycidyl ether.

  Examples of the vinyl ether monomer include methyl vinyl ether, ethyl vinyl ether, isobutyl vinyl ether, and the like.

  Examples of the alkyl (meth) acrylate having an alkyl group having 1 carbon atom include methyl (meth) acrylate.

  Examples of the alkyl (meth) acrylate having an alkyl group having 10 or more carbon atoms include decyl (meth) acrylate, dodecyl (meth) acrylate, and tetradecyl (meth) acrylate.

  In the present invention, other polymerizable monomers may be used alone or in combination of two or more, but the total content is 0 to 5% by weight as a monomer unit. It is preferable that it is 0 to 3% by weight.

  Furthermore, examples of copolymerizable monomers other than the above include silane monomers containing silicon atoms. Examples of the silane monomer include 3-acryloxypropyltriethoxysilane, vinyltrimethoxysilane, vinyltriethoxysilane, 4-vinylbutyltrimethoxysilane, 4-vinylbutyltriethoxysilane, and 8-vinyloctyltrimethoxysilane. 8-vinyloctyltriethoxysilane, 10-methacryloyloxydecyltrimethoxysilane, 10-acryloyloxydecyltrimethoxysilane, 10-methacryloyloxydecyltriethoxysilane, 10-acryloyloxydecyltriethoxysilane, and the like.

  The silane monomer may be used alone, or two or more kinds may be mixed and used. However, the total content of the silane monomer is 0.00 with respect to 100 parts by weight of the (meth) acrylic polymer. It is preferable that it is 1-3 weight part, and it is more preferable that it is 0.5-2 weight part. Copolymerization of a silane monomer is preferable for improving durability.

  The weight average molecular weight of the acrylic polymer is 1.5 million or more, and preferably 2 million to 3 million. When the weight average molecular weight is less than 1,500,000, the resulting pressure-sensitive adhesive layer has poor durability.

  The proportion of the acrylic polymer having a molecular weight of 100,000 or less is 20% by weight or less, and preferably 15% by weight is preferable from the viewpoint of crosslinkability. In the present invention, since the entanglement of the molecular chains is reduced by adding a poor solvent, if there are many low molecular weight products, the crosslinkability between the polymer molecular chains becomes very poor, so the lower the low molecular weight products, the better. .

  The molecular weight of the polymer in the present invention refers to that measured by the method described in Examples. Moreover, the component ratio of molecular weight 100,000 or less also refers to what was measured by the method as described in an Example.

  For the production of such an acrylic polymer, it is preferable to select a radical polymerization method using an organic solvent. This is because in a polymerization method using water as represented by emulsion polymerization, it is necessary to dry the water once and then add a predetermined amount of the solvent of the present invention, which is not economical.

  As the radical polymerization initiator, various known azo and peroxide initiators can be used. For example, in solution polymerization, a polymerization initiator such as azobisinbutyronitrile is used in an amount of about 0.01 to 0.2 parts by weight with respect to 100 parts by weight of the total amount of monomers. As the polymerization solvent, for example, a good solvent such as ethyl acetate or toluene is used. The reaction is usually carried out at about 50 to 70 ° C. for about 8 to 15 hours under an inert gas stream such as nitrogen. The residual monomer after polymerization is regarded as a good solvent for the acrylic polymer.

With regard to solubility theory, Hildebrand proposed a basic theory of solubility and solubility parameters from 1936 to 1950 (J. Hildebrand, RL Scott The Solidability of Nonelectrolytes, Rheinhold, NY (1950). According to this, the enthalpy of mixing when the two substances 1 and 2 are mixed is as follows:
ΔH = V1 (δ1-δ2) 2φ22
Here, V1 = molar volume of substance 1, δ1, δ2 = SP value of substance 1 and substance 2, φ2 = volume fraction of substance 2, and dissolution occurs when δ1 and δ2 are equal or close to each other.

In the present invention, the solubility parameter (SP value) of the homopolymer of the main monomer unit (the one with the highest content) constituting the acrylic polymer, not the solvent (good solvent) in which the acrylic polymer is easily compatible. ) Is δ1 “(J / cm ³ ) ^1/2 ”, the solubility parameter (SP value) such that the difference in solubility parameter (SP value) (Δδ = δ1-δ2) is +1.7 to +5 ) A poor solvent having δ2 [(J / cm ³ ) ^1/2 ] is contained in an amount of 20 to 60% by weight of the total amount of the organic solvent. A preferable solubility parameter (SP value) difference (Δδ = δ1-δ2) is +2 to +5. By adding a prescribed amount of such a poor solvent, the viscosity of the pressure-sensitive adhesive composition is reduced. The SP value of various solvents can be easily calculated from the measurement of latent heat of vaporization and boiling point.

  The SP value (solubility parameter) of a polymer is measured by measuring the intrinsic viscosity of the polymer, measuring the cloud point when a non-solvent is dropped into a dilute solution of the polymer, and the maximum swelling ratio of the polymer in various solvents. The method of measuring is taken. As the SP value of the acrylic polymer of the present invention, the SP value shown in Table 1 based on the actual measurement value of the maximum swelling ratio as described in the reference was applied. Reference: Polymer Handbook 3rd edition, publisher Wiley Interscience, Toshinao Okitsu, Journal of the Adhesion Society of Japan, 29 (5) 204 (1993).

  Examples of the poor solvent for the acrylic polymer of the present invention include n-hexane, n-heptane, n-octane and isomers thereof, and some of them are listed in Table 2. References: New edition of the Solvent Pocket Book, Editors Association of Synthetic Organic Chemistry, Publisher Ohm Co., 1994.

  In general, it is known that a polymer domain expands in a good solvent and conversely contracts in a poor solvent to lower the viscosity of the solution. Also in the present invention, when a poor solvent is added, the viscosity decreases, so that a good coated surface can be obtained even with a small amount of solvent. However, in the case of the acrylic polymer of the present invention, when the amount of the poor solvent exceeds 60% by weight of the total amount of the organic solvent, the polymer is prayed and cannot be applied. In the present invention, the poor solvent is best in the range of 20 to 60% by weight, preferably 40 to 55% by weight of the total amount of the organic solvent. In addition, when using the some poor solvent from which (triangle | delta) delta becomes the said range, it is preferable to make the total content which totaled the content of each poor solvent into the said range.

  There is a multi-angle light scattering (MALLLS) method as a method for measuring the spread of molecular chains of a polymer chain. As a measurement procedure, first, the refractive index is measured by changing the polymer concentration, and dn / dc is measured. Then, MALLLS measurement is performed by microbatch measurement, and a z-mean square turning radius (Rz) is obtained by a Zimm plot.

  Refractive index measurement of the solvent was performed with an apparatus: Atago, Abbe refractometer 1T, wavelength: 589 nm, and for the measurement apparatus, a microbatch measurement was performed using a GPC apparatus, and a stainless tube was connected instead of a GPC column. .

MALLS detector: Wyatt Technology, DAWN DSP-F
(17 photodiodes installed at different scattering angles)
Laser wavelength: 632.8 nm
Multi-angle fitting method: Berry method Column tank temperature: 40 ° C
Flow rate: 0.7mm / min
Concentration: 0.02, 0.03, 0.04, 0.05%

  In the acrylic polymer of the present invention (weight average molecular weight of 2.2 million, molecular weight of 100,000 or less 2% by weight), Rz = 110 nm at 100% ethyl acetate, whereas n-heptane which is a poor solvent is 50% by weight. (Ethyl acetate: n-heptane 50% by weight: 50% by weight) When mixed, it was confirmed that Rz was reduced to 93 nm.

  Thus, although it is known that the addition of a poor solvent such as a hydrocarbon decreases the viscosity, the main reason why the poor solvent is not actually used is that the addition of the poor solvent causes the polymer molecular chains to It is presumed that it is difficult to form a crosslinked structure. That is, in a poor solvent such as hydrocarbon, the entanglement of molecular chains is reduced, and the formation of a cross-linked structure between polymer molecular chains is very unlikely. As a result, it is assumed that the durability is deteriorated. . For this reason, in the present invention, it is very important to control the molecular weight of the (meth) acrylic polymer that is the base polymer, and the component ratio of the (meth) acrylic polymer having a weight average molecular weight of 1,500,000 or more and a molecular weight of 100,000 or less. Is 20% by weight or less to solve the above problem.

  The boiling point of the poor solvent and the boiling point (b.p .: boiling point) of the good solvent are not particularly limited, but it is preferable for coating and drying that the difference is not more than 50 ° C. When the difference between the boiling point of the poor solvent and the boiling point of the good solvent that dissolves the (meth) acrylic polymer is large, the good solvent vaporizes and evaporates first during coating, so that the polymer is precipitated and coated. In some cases, the workability is remarkably deteriorated. In addition, it shows in Table 3 about the boiling point (b.p.:boiling point) of the typical poor solvent in this invention.

  The good solvent for the (meth) acrylic polymer of the present invention is not particularly limited as long as it is a solvent capable of dissolving the (meth) acrylic polymer, but ethyl acetate, toluene, cyclohexanone, methyl ethyl ketone, etc. used during polymerization Can be used as appropriate.

  In the present invention, the boiling point of the poor solvent is preferably 165 ° C. or less, more preferably 155 ° C. or less, and further preferably 145 ° C. or less. If the boiling point of the poor solvent becomes too high, the solvent remains in the pressure-sensitive adhesive layer even after drying, resulting in a tendency to deteriorate the adhesive properties and inferior in durability (for example, problems such as foaming occur in the durability test). is there.

  In this invention, it is preferable to contain 0.01-5 weight part of crosslinking agents with respect to 100 weight part of acrylic polymers. The crosslinking agent is a polyfunctional compound capable of forming a crosslinked structure by reacting with a carboxylic acid group of an acrylic polymer and further with another functional group.

  When a hydroxyl group is introduced as a functional group, a crosslinked structure is formed with the hydroxyl group. Examples of the crosslinking agent include tolylene diisocyanate, diphenylmethane diisocyanate, polyisocyanate compounds such as adducts of these diisocyanate compounds to various polyols, epoxy compounds, aziridine compounds, melamine compounds, metal salt metal chelate compounds, and the like. Of these, polyisocyanate compounds are preferably used. In particular, when an acrylic polymer is produced, a hydroxyl group-containing monomer such as 2-hydroxyethyl acrylate is copolymerized to introduce a hydroxyl group into the acrylic polymer. It is preferable to form a crosslinked structure of the polymer.

  In the present invention, the gel fraction after crosslinking is preferably 45 to 95% by weight, more preferably 50 to 85% by weight. With such a gel fraction, the durability at high temperature is excellent. The gel fraction indicates the degree of crosslinking and is the ratio of the portion crosslinked with the pressure-sensitive adhesive. This gel fraction points out what was measured by the method as described in an Example.

  Moreover, it is preferable to contain 0.01-1 weight part of silane coupling agents with respect to 100 weight part of said acrylic polymers. As the silane coupling agent, those conventionally known can be used without particular limitation. For example, epoxy group-containing silane coupling agents such as 3-glycidoxypropyltrimethoxysilane, 3-glycidoxypropylmethyldiethoxysilane, 2- (3,4-epoxycyclohexyl) ethyltrimethoxysilane; 3-amino Amino group-containing silane coupling agents such as propyltrimethoxysilane, N-2- (aminoethyl) -3-aminopropylmethyldimethoxysilane, 3-triethoxysilyl-N- (1,3-dimethylbutylidene) propylamine A (meth) acrylic group-containing silane coupling agent such as 3-acryloxypropyltrimethoxysilane or 3-methacryloxypropyltriethoxysilane; an isocyanate group-containing silane coupling agent such as 3-isocyanatopropyltriethoxysilane; Fried That. These compounds may be used alone or in combination of two or more.

  The pressure-sensitive adhesive composition of the present invention can be blended with an ultraviolet absorber, an anti-aging agent, a softening agent, a dye, a pigment, a filler and the like, if necessary.

  The pressure-sensitive adhesive optical member of the present invention is obtained by forming a pressure-sensitive adhesive layer on one side or both sides of the optical member with the pressure-sensitive adhesive composition for optical members. The method of forming the pressure-sensitive adhesive layer on the optical member is not particularly limited, and the pressure-sensitive adhesive composition is applied to a release-treated support (release sheet), dried and crosslinked to form a pressure-sensitive adhesive layer. And a method of forming a pressure-sensitive adhesive layer by applying a pressure-sensitive adhesive composition directly to the optical member, drying and crosslinking treatment, and the like. As a coating method, any coating method such as a roll coater such as a comma coater, a reverse coater or a gravure coater, a curtain coater, a lip coater or a die coater can be adopted.

  The solid content concentration of the pressure-sensitive adhesive composition solution is preferably 10 to 30% by weight. More preferably, the content is 12 to 20% by weight. There is a proportional relationship between the concentration and the viscosity of the polymer solution. If the concentration is too high, the viscosity also increases and streaks or the like are generated during coating. Therefore, the viscosity obtained by the measurement method described in the examples is 7000 [mPa · sec] or less, preferably 5000 [mPa · sec] or less.

  The thickness of the pressure-sensitive adhesive layer after drying is 1 to 100 μm, particularly 5 to 40 μm, preferably 10 to 30 μm. When the thickness of the pressure-sensitive adhesive layer is 100 μm or more, the present invention contains a poor solvent, so that streaks during coating and haze during drying are likely to occur.

  When the adhesive layer is exposed on such a surface, it is protected with a peeled sheet until it is put to practical use. As the constituent material of the release sheet, paper, polyethylene, polypropylene, polyethylene terephthalate and other synthetic resin films, rubber sheets, paper, cloth, non-woven fabric, nets, foam sheets and metal foils, laminates thereof, and other suitable thin leaves Such as body. The surface of the release sheet may be subjected to a release treatment such as silicone treatment, long-chain alkyl treatment, or fluorine treatment as necessary in order to enhance the peelability from the pressure-sensitive adhesive layer.

  An optical member used for forming a liquid crystal display device or the like is used, and the type thereof is not particularly limited. For example, the optical member includes a polarizing plate. A polarizing plate having a transparent protective film on one or both sides of a polarizer is generally used.

  The polarizer is not particularly limited, and various types can be used. Examples of the polarizer include hydrophilic polymer films such as polyvinyl alcohol film, partially formalized polyvinyl alcohol film, and ethylene / vinyl acetate copolymer partially saponified film, and two colors such as iodine and dichroic dye. Examples thereof include polyene-based oriented films such as those obtained by adsorbing volatile substances and uniaxially stretched, polyvinyl alcohol dehydrated products and polyvinyl chloride dehydrochlorinated products. Among these, a polarizer composed of a polyvinyl alcohol film and a dichroic material such as iodine is preferable. The thickness of these polarizers is not particularly limited, but is generally about 5 to 80 μm.

  A polarizer obtained by dyeing a polyvinyl alcohol film with iodine and uniaxially stretching it can be produced, for example, by dyeing polyvinyl alcohol in an aqueous solution of iodine and stretching it 3 to 7 times the original length. If necessary, it can be immersed in an aqueous solution such as potassium iodide which may contain boric acid, zinc sulfate, zinc chloride and the like. Further, if necessary, the polyvinyl alcohol film may be immersed in water and washed before dyeing. In addition to washing the polyvinyl alcohol film surface with dirt and anti-blocking agents by washing the polyvinyl alcohol film with water, it also has the effect of preventing unevenness such as uneven coloring by swelling the polyvinyl alcohol film. is there. Stretching may be performed after dyeing with iodine, or may be performed while dyeing, or may be performed with dyeing after iodine. The film can be stretched in an aqueous solution of boric acid or potassium iodide or in a water bath.

  As a material for forming the transparent protective film provided on one side or both sides of the polarizer, a material excellent in transparency, mechanical strength, thermal stability, moisture shielding property, isotropy and the like is preferable. For example, polyester polymers such as polyethylene terephthalate and polyethylene naphthalate, cellulose polymers such as diacetyl cellulose and triacetyl cellulose, acrylic polymers such as polymethyl methacrylate, styrene such as polystyrene and acrylonitrile / styrene copolymer (AS resin) -Based polymer, polycarbonate-based polymer and the like. In addition, polyethylene, polypropylene, polyolefins having a cyclo or norbornene structure, polyolefin polymers such as ethylene / propylene copolymers, vinyl chloride polymers, amide polymers such as nylon and aromatic polyamide, imide polymers, sulfone polymers , Polyether sulfone polymer, polyether ether ketone polymer, polyphenylene sulfide polymer, vinyl alcohol polymer, vinylidene chloride polymer, vinyl butyral polymer, arylate polymer, polyoxymethylene polymer, epoxy polymer, or the above Polymer blends and the like are also examples of polymers that form the transparent protective film. The transparent protective film can also be formed as a cured layer of thermosetting or ultraviolet curable resin such as acrylic, urethane, acrylurethane, epoxy, and silicone.

  Moreover, the polymer film described in JP-A-2001-343529 (WO01 / 37007), for example, (A) a thermoplastic resin having a substituted and / or unsubstituted imide group in the side chain, and (B) a substitution in the side chain And / or a resin composition containing an unsubstituted phenyl and a thermoplastic resin having a nitrile group. A specific example is a film of a resin composition containing an alternating copolymer composed of isobutylene and N-methylmaleimide and an acrylonitrile / styrene copolymer. As the film, a film made of a mixed extruded product of the resin composition or the like can be used.

  Although the thickness of a protective film can be determined suitably, generally it is about 1-500 micrometers from points, such as workability | operativity, such as intensity | strength and handleability, and thin layer property. 1-300 micrometers is especially preferable, and 5-200 micrometers is more preferable.

  Moreover, it is preferable that a protective film has as little color as possible. Therefore, Rth = [(nx + ny) / 2−nz] · d (where nx and ny are the main refractive index in the plane of the film, nz is the refractive index in the film thickness direction, and d is the film thickness). A protective film having a retardation value in the film thickness direction of −90 nm to +75 nm is preferably used. By using a film having a thickness direction retardation value (Rth) of −90 nm to +75 nm, the coloring (optical coloring) of the polarizing plate caused by the protective film can be almost eliminated. The thickness direction retardation value (Rth) is more preferably −80 nm to +60 nm, and particularly preferably −70 nm to +45 nm.

  As the protective film, a cellulose polymer such as triacetyl cellulose is preferable from the viewpoints of polarization characteristics and durability. A triacetyl cellulose film is particularly preferable. In addition, when providing a protective film in the both sides of a polarizer, the protective film which consists of the same polymer material may be used by the front and back, and the protective film which consists of a different polymer material etc. may be used. The polarizer and the protective film are usually in close contact with each other through an aqueous adhesive or the like. Examples of the water-based adhesive include an isocyanate-based adhesive, a polyvinyl alcohol-based adhesive, a gelatin-based adhesive, a vinyl-based latex, a water-based polyurethane, and a water-based polyester.

  The surface of the transparent protective film to which the polarizer is not adhered may be subjected to a hard coat layer, an antireflection treatment, an antisticking treatment, or a treatment for diffusion or antiglare.

  Hard coat treatment is applied for the purpose of preventing scratches on the surface of the polarizing plate. For example, a transparent protective film with a cured film excellent in hardness, sliding properties, etc. by an appropriate ultraviolet curable resin such as acrylic or silicone It can be formed by a method of adding to the surface of the film. The antireflection treatment is performed for the purpose of preventing reflection of external light on the surface of the polarizing plate, and can be achieved by forming an antireflection film or the like according to the conventional art. Further, the anti-sticking treatment is performed for the purpose of preventing adhesion with an adjacent layer.

  Anti-glare treatment is applied for the purpose of preventing external light from being reflected on the surface of the polarizing plate and obstructing the visibility of light transmitted through the polarizing plate. For example, a roughening method using a sandblasting method or an embossing method. It can be formed by imparting a fine concavo-convex structure to the surface of the transparent protective film by an appropriate method such as a blending method of transparent fine particles. The fine particles to be included in the formation of the surface fine concavo-convex structure are, for example, conductive materials made of silica, alumina, titania, zirconia, tin oxide, indium oxide, cadmium oxide, antimony oxide or the like having an average particle diameter of 0.5 to 50 μm. In some cases, transparent fine particles such as inorganic fine particles, organic fine particles made of a crosslinked or uncrosslinked polymer, and the like are used. When forming a surface fine uneven structure, the amount of fine particles used is generally about 2 to 50 parts by weight, preferably 5 to 25 parts by weight, based on 100 parts by weight of the transparent resin forming the surface fine uneven structure. The antiglare layer may also serve as a diffusion layer (viewing angle expanding function or the like) for diffusing the light transmitted through the polarizing plate to expand the viewing angle.

  The antireflection layer, antisticking layer, diffusion layer, antiglare layer, and the like can be provided on the transparent protective film itself, or can be provided separately from the transparent protective film as an optical layer.

  The optical member of the present invention includes, for example, a liquid crystal display device such as a reflecting plate, a semi-transmissive plate, a retardation plate (including wavelength plates such as 1/2 and 1/4), a viewing angle compensation film, and a brightness enhancement film. What becomes an optical layer which may be used for formation is mention | raise | lifted. These can be used alone as the optical member of the present invention, and can be laminated on the polarizing plate for practical use and used in one or more layers.

  In particular, a reflective polarizing plate or semi-transmissive polarizing plate in which a polarizing plate is further laminated with a reflecting plate or a semi-transmissive reflecting plate, an elliptical polarizing plate or circular polarizing plate in which a retardation plate is further laminated on a polarizing plate, a polarizing plate A wide viewing angle polarizing plate in which a viewing angle compensation film is further laminated on a plate, or a polarizing plate in which a brightness enhancement film is further laminated on a polarizing plate is preferable.

  A reflective polarizing plate is a polarizing plate provided with a reflective layer, and is used to form a liquid crystal display device or the like that reflects incident light from the viewing side (display side). Such a light source can be omitted, and the liquid crystal display device can be easily thinned. The reflective polarizing plate can be formed by an appropriate method such as a method in which a reflective layer made of metal or the like is attached to one surface of the polarizing plate via a transparent protective layer or the like as necessary.

  Specific examples of the reflective polarizing plate include those in which a reflective layer is formed by attaching a foil or a vapor deposition film made of a reflective metal such as aluminum on one side of a transparent protective film matted as necessary. Moreover, the transparent protective film contains fine particles so as to have a surface fine concavo-convex structure and a reflective layer having a fine concavo-convex structure thereon. The reflective layer having the fine concavo-convex structure has an advantage that incident light is diffused by irregular reflection to prevent directivity and glaring appearance and to suppress unevenness in brightness and darkness. The transparent protective film containing fine particles also has an advantage that incident light and its reflected light are diffused when passing through it, and light and dark unevenness can be further suppressed. The reflective layer with the fine concavo-convex structure reflecting the surface fine concavo-convex structure of the transparent protective film is formed by transparent the metal by an appropriate method such as a vacuum evaporation method, an ion plating method, a sputtering method, or a plating method. It can be performed by a method of directly attaching to the surface of the protective layer.

  Instead of the method of directly applying the reflecting plate to the transparent protective film of the polarizing plate, the reflecting plate can be used as a reflecting sheet provided with a reflecting layer on an appropriate film according to the transparent film. Since the reflective layer is usually made of metal, the usage form in which the reflective surface is covered with a transparent protective film, a polarizing plate or the like is used to prevent the reflectance from being lowered due to oxidation, and thus to maintain the initial reflectance for a long time. In addition, it is more preferable to avoid a separate attachment of the protective layer.

  The semi-transmissive polarizing plate can be obtained by using a semi-transmissive reflective layer such as a half mirror that reflects and transmits light with the reflective layer. A transflective polarizing plate is usually provided on the back side of a liquid crystal cell, and displays an image by reflecting incident light from the viewing side (display side) when a liquid crystal display device is used in a relatively bright atmosphere. In a relatively dark atmosphere, a liquid crystal display device or the like that displays an image using a built-in light source such as a backlight built in the back side of the transflective polarizing plate can be formed. In other words, the transflective polarizing plate is useful for forming a liquid crystal display device of a type that can save energy of using a light source such as a backlight in a bright atmosphere and can be used with a built-in light source even in a relatively dark atmosphere. It is.

  An elliptically polarizing plate or a circularly polarizing plate in which a retardation plate is further laminated on a polarizing plate will be described. A phase difference plate or the like is used when changing linearly polarized light to elliptically polarized light or circularly polarized light, changing elliptically polarized light or circularly polarized light to linearly polarized light, or changing the polarization direction of linearly polarized light. In particular, a so-called quarter-wave plate (also referred to as a λ / 4 plate) is used as a retardation plate that changes linearly polarized light into circularly polarized light or changes circularly polarized light into linearly polarized light. A half-wave plate (also referred to as a λ / 2 plate) is usually used when changing the polarization direction of linearly polarized light.

  The elliptically polarizing plate is effectively used for black-and-white display without the above color by compensating (preventing) the coloration (blue or yellow) generated by the birefringence of the liquid crystal layer of the super twist nematic (STN) type liquid crystal display device. It is done. Further, the one in which the three-dimensional refractive index is controlled is preferable because it can compensate (prevent) coloring that occurs when the screen of the liquid crystal display device is viewed from an oblique direction. The circularly polarizing plate is effectively used, for example, when adjusting the color tone of an image of a reflective liquid crystal display device in which the image is displayed in color, and also has an antireflection function.

  Examples of the retardation plate include a birefringent film obtained by uniaxially or biaxially stretching a polymer material, a liquid crystal polymer alignment film, and a liquid crystal polymer alignment layer supported by a film. The thickness of the retardation plate is not particularly limited, but is generally about 20 to 150 μm.

  Examples of the polymer material include polyvinyl alcohol, polyvinyl butyral, polymethyl vinyl ether, polyhydroxyethyl acrylate, hydroxyethyl cellulose, hydroxypropyl cellulose, methyl cellulose, polycarbonate, polyarylate, polysulfone, polyethylene terephthalate, polyethylene naphthalate, polyether sulfone, Polyphenylene sulfide, polyphenylene oxide, polyallylsulfone, polyvinyl alcohol, polyamide, polyimide, polyolefin, polyvinyl chloride, cellulose polymer, norbornene resin, or binary, ternary various copolymers, graft copolymers Examples thereof include polymers and blends. These polymer materials become oriented products (stretched films) by stretching or the like.

  Examples of the liquid crystalline polymer include various main chain types and side chain types in which a conjugated linear atomic group (mesogen) imparting liquid crystal alignment is introduced into the main chain or side chain of the polymer. It is done. Specific examples of the main chain type liquid crystalline polymer include nematic alignment polyester liquid crystalline polymer, discotic polymer, cholesteric polymer, and the like having a structure in which a mesogenic group is bonded to a spacer portion that imparts flexibility. . Specific examples of the side chain type liquid crystalline polymer include polysiloxane, polyacrylate, polymethacrylate, or polymalonate as a main chain skeleton, and a nematic alignment imparting paraffin through a spacer portion composed of a conjugated atomic group as a side chain. Examples thereof include those having a mesogen moiety composed of a substituted cyclic compound unit. These liquid crystalline polymers are prepared by, for example, applying a solution of a liquid crystalline polymer on an alignment surface such as those obtained by rubbing the surface of a thin film such as polyimide or polyvinyl alcohol formed on a glass plate, or by obliquely depositing silicon oxide. This is done by developing and heat treatment.

  The retardation plate may have an appropriate retardation according to the purpose of use, such as those for the purpose of compensating for various wavelength plates or birefringence of liquid crystal layers and compensation of viewing angle, etc. What laminated | stacked the phase difference plate and controlled optical characteristics, such as phase difference, etc. may be used.

  The elliptical polarizing plate and the reflective elliptical polarizing plate are obtained by laminating a polarizing plate or a reflective polarizing plate and a retardation plate in an appropriate combination. Such an elliptically polarizing plate or the like can also be formed by sequentially laminating them sequentially in the manufacturing process of the liquid crystal display device so as to be a combination of a (reflective) polarizing plate and a retardation plate. An optical member such as a polarizing plate has an advantage that it can improve the production efficiency of a liquid crystal display device and the like because of excellent quality stability and lamination workability.

  The viewing angle compensation film is a film for widening the viewing angle so that the image can be seen relatively clearly even when the screen of the liquid crystal display device is viewed from a slightly oblique direction rather than perpendicular to the screen. As such a viewing angle compensation phase difference plate, for example, a phase difference plate, an alignment film such as a liquid crystal polymer, or an alignment layer such as a liquid crystal polymer supported on a transparent substrate is used. A normal retardation plate uses a birefringent polymer film uniaxially stretched in the plane direction, whereas a retardation plate used as a viewing angle compensation film stretches biaxially in the plane direction. Birefringent polymer film, biaxially stretched film such as polymer with birefringence with a controlled refractive index in the thickness direction that is uniaxially stretched in the plane direction and stretched in the thickness direction, etc. Used. Examples of the inclined alignment film include a film obtained by bonding a heat shrink film to a polymer film and stretching or / and shrinking the polymer film under the action of the contraction force by heating, or a film obtained by obliquely aligning a liquid crystal polymer. can give. The raw material polymer for the phase difference plate is the same as the polymer described in the previous phase difference plate, preventing coloration due to a change in the viewing angle based on the phase difference by the liquid crystal cell and expanding the viewing angle for good visual recognition. An appropriate one for the purpose can be used.

  Also, from the viewpoint of achieving a wide viewing angle with good visibility, an optically compensated phase difference in which a liquid crystal polymer alignment layer, in particular an optically anisotropic layer composed of a discotic liquid crystal polymer gradient alignment layer, is supported by a triacetylcellulose film. A plate can be preferably used.

  A polarizing plate obtained by bonding a polarizing plate and a brightness enhancement film is usually provided on the back side of a liquid crystal cell. The brightness enhancement film reflects a linearly polarized light with a predetermined polarization axis or a circularly polarized light in a predetermined direction when natural light is incident due to a backlight such as a liquid crystal display device or reflection from the back side, and transmits other light. In addition, a polarizing plate in which a brightness enhancement film is laminated with a polarizing plate allows light from a light source such as a backlight to enter to obtain transmitted light in a predetermined polarization state, and reflects light without transmitting the light other than the predetermined polarization state. The The light reflected on the surface of the brightness enhancement film is further inverted through a reflective layer provided on the rear side thereof and re-incident on the brightness enhancement film, and a part or all of the light is transmitted as light in a predetermined polarization state. Luminance can be improved by increasing the amount of light transmitted through the enhancement film and increasing the amount of light that can be used for liquid crystal display image display or the like by supplying polarized light that is difficult to be absorbed by the polarizer. That is, when light is incident through the polarizer from the back side of the liquid crystal cell without using a brightness enhancement film, light having a polarization direction that does not coincide with the polarization axis of the polarizer is almost polarized. It is absorbed by the polarizer and does not pass through the polarizer. That is, although depending on the characteristics of the polarizer used, approximately 50% of the light is absorbed by the polarizer, and the amount of light that can be used for liquid crystal image display or the like is reduced accordingly, resulting in a dark image. The brightness enhancement film allows light having a polarization direction that is absorbed by the polarizer to be reflected once by the brightness enhancement film without being incident on the polarizer, and then inverted through a reflective layer or the like provided behind the brightness enhancement film. Repeatedly re-enter the brightness enhancement film, and the brightness enhancement film transmits only polarized light whose polarization direction is such that the polarization direction of light reflected and inverted between the two can pass through the polarizer. Therefore, light such as a backlight can be efficiently used for displaying an image on the liquid crystal display device, and the screen can be brightened.

  A diffusion plate may be provided between the brightness enhancement film and the reflective layer. The polarized light reflected by the brightness enhancement film is directed to the reflective layer or the like, but the installed diffuser plate uniformly diffuses the light passing therethrough and simultaneously cancels the polarized state and becomes a non-polarized state. That is, the diffuser plate returns the polarized light to the original natural light state. The light in the non-polarized state, that is, the natural light state is directed to the reflection layer and the like, reflected through the reflection layer and the like, and again passes through the diffusion plate and reenters the brightness enhancement film. Thus, while maintaining the brightness of the display screen by providing a diffuser plate that returns polarized light to the original natural light state between the brightness enhancement film and the reflective layer, etc., the brightness unevenness of the display screen is reduced at the same time, A uniform and bright screen can be provided. By providing such a diffuser plate, it is considered that the first incident light has a moderate increase in the number of repetitions of reflection, and in combination with the diffusion function of the diffuser plate, a uniform bright display screen can be provided.

  The brightness enhancement film has a characteristic of transmitting linearly polarized light having a predetermined polarization axis and reflecting other light, such as a multilayer thin film of dielectric or a multilayer laminate of thin film having different refractive index anisotropy. Such as an alignment film of a cholesteric liquid crystal polymer or an alignment liquid crystal layer supported on a film substrate, which reflects either left-handed or right-handed circularly polarized light and transmits other light. Appropriate things such as a thing can be used.

  Therefore, in the brightness enhancement film of the type that transmits linearly polarized light having the predetermined polarization axis as described above, the transmitted light is incident on the polarizing plate with the polarization axis aligned as it is, thereby efficiently transmitting while suppressing absorption loss due to the polarizing plate. Can be made. On the other hand, in a brightness enhancement film of a type that emits circularly polarized light such as a cholesteric liquid crystal layer, it can be directly incident on a polarizer. It is preferable to make it enter into a polarizing plate. Note that circularly polarized light can be converted to linearly polarized light by using a quarter wave plate as the retardation plate.

  A retardation plate that functions as a quarter-wave plate in a wide wavelength range such as a visible light region exhibits, for example, a retardation layer that functions as a quarter-wave plate for light-color light having a wavelength of 550 nm and other retardation characteristics. It can be obtained by a method of superposing a retardation layer, for example, a retardation layer functioning as a half-wave plate. Therefore, the retardation plate disposed between the polarizing plate and the brightness enhancement film may be composed of one or more retardation layers.

  In addition, the cholesteric liquid crystal layer can also be obtained by reflecting circularly polarized light in a wide wavelength range such as the visible light region by combining two or more layers with different reflection wavelengths and having an overlapping structure. Based on this, transmitted circularly polarized light in a wide wavelength range can be obtained.

  Further, the polarizing plate may be formed by laminating a polarizing plate and two or three or more optical layers like the above-described polarization separation type polarizing plate. Therefore, a reflective elliptical polarizing plate or a semi-transmissive elliptical polarizing plate in which the above-mentioned reflective polarizing plate or transflective polarizing plate and a retardation plate are combined may be used.

  The optical member in which the optical layer is laminated on the polarizing plate can be formed by a method of sequentially laminating separately in the manufacturing process of a liquid crystal display device or the like. There is an advantage that the manufacturing process of the liquid crystal display device and the like can be improved. For the lamination, an appropriate adhesive means such as an adhesive layer can be used. When adhering the polarizing plate and the other optical layer, their optical axes can be set at an appropriate arrangement angle in accordance with the target phase difference characteristic.

  In addition, each layer such as an optical member or an adhesive layer of the pressure-sensitive adhesive optical member of the present invention includes, for example, ultraviolet rays such as a salicylic acid ester compound, a benzophenol compound, a benzotriazole compound, a cyanoacrylate compound, and a nickel complex compound. What gave the ultraviolet absorptivity by systems, such as a system processed with an absorber, may be used.

  The pressure-sensitive adhesive optical member of the present invention can be preferably used for forming various image display devices such as a liquid crystal display device. The liquid crystal display device can be formed according to the conventional method. That is, a liquid crystal display device is generally formed by appropriately assembling components such as a liquid crystal cell, an adhesive optical member, and an illumination system as necessary, and incorporating a drive circuit. There is no particular limitation except that an optical member is used. As the liquid crystal cell, any type such as a TN type, an STN type, or a π type can be used.

  An appropriate liquid crystal display device such as a liquid crystal display device in which an adhesive optical member is disposed on one side or both sides of a liquid crystal cell, or a backlight or a reflector used in an illumination system can be formed. In that case, the optical member by this invention can be installed in the one side or both sides of a liquid crystal cell. When optical members are provided on both sides, they may be the same or different. Further, when forming a liquid crystal display device, for example, a single layer or a suitable part such as a diffusing plate, an antiglare layer, an antireflection film, a protective plate, a prism array, a lens array sheet, a light diffusing plate, a backlight, etc. Two or more layers can be arranged.

  Next, an organic electroluminescence device (organic EL display device) will be described. Generally, in an organic EL display device, a transparent electrode, an organic light emitting layer, and a metal electrode are sequentially laminated on a transparent substrate to form a light emitter (organic electroluminescent light emitter). Here, the organic light emitting layer is a laminate of various organic thin films, for example, a laminate of a hole injection layer made of a triphenylamine derivative and the like and a light emitting layer made of a fluorescent organic solid such as anthracene, Alternatively, a structure having various combinations such as a laminate of such a light emitting layer and an electron injection layer composed of a perylene derivative or the like, or a laminate of these hole injection layer, light emitting layer, and electron injection layer is known. It has been.

  In organic EL display devices, holes and electrons are injected into the organic light-emitting layer by applying a voltage to the transparent electrode and the metal electrode, and the energy generated by recombination of these holes and electrons excites the phosphor material. Then, light is emitted on the principle that the excited fluorescent material emits light when returning to the ground state. The mechanism of recombination in the middle is the same as that of a general diode, and as can be predicted from this, the current and the emission intensity show strong nonlinearity with rectification with respect to the applied voltage.

  In an organic EL display device, in order to extract light emitted from the organic light emitting layer, at least one of the electrodes must be transparent, and a transparent electrode usually formed of a transparent conductor such as indium tin oxide (ITO) is used as an anode. It is used as. On the other hand, in order to facilitate electron injection and increase luminous efficiency, it is important to use a material having a small work function for the cathode, and usually metal electrodes such as Mg—Ag and Al—Li are used.

  In the organic EL display device having such a configuration, the organic light emitting layer is formed of a very thin film having a thickness of about 10 nm. For this reason, the organic light emitting layer transmits light almost completely like the transparent electrode. As a result, light that is incident from the surface of the transparent substrate at the time of non-light emission, passes through the transparent electrode and the organic light emitting layer, and is reflected by the metal electrode is again emitted to the surface side of the transparent substrate. The display surface of the organic EL display device looks like a mirror surface.

  In an organic EL display device comprising an organic electroluminescent light emitting device comprising a transparent electrode on the surface side of an organic light emitting layer that emits light upon application of a voltage and a metal electrode on the back side of the organic light emitting layer, the surface of the transparent electrode While providing a polarizing plate on the side, a retardation plate can be provided between the transparent electrode and the polarizing plate.

  Since the retardation plate and the polarizing plate have a function of polarizing light incident from the outside and reflected by the metal electrode, there is an effect that the mirror surface of the metal electrode is not visually recognized by the polarization action. In particular, the mirror surface of the metal electrode can be completely shielded by configuring the retardation plate with a quarter-wave plate and adjusting the angle formed by the polarization direction of the polarizing plate and the retardation plate to π / 4. .

  That is, only the linearly polarized light component of the external light incident on the organic EL display device is transmitted by the polarizing plate. This linearly polarized light becomes generally elliptically polarized light by the phase difference plate, but becomes circularly polarized light particularly when the phase difference plate is a quarter wavelength plate and the angle formed by the polarization direction of the polarizing plate and the phase difference plate is π / 4. .

  This circularly polarized light is transmitted through the transparent substrate, the transparent electrode, and the organic thin film, is reflected by the metal electrode, is again transmitted through the organic thin film, the transparent electrode, and the transparent substrate, and becomes linearly polarized light again on the retardation plate. And since this linearly polarized light is orthogonal to the polarization direction of a polarizing plate, it cannot permeate | transmit a polarizing plate. As a result, the mirror surface of the metal electrode can be completely shielded.

  EXAMPLES The present invention will be specifically described below based on examples, but the present invention is not limited to these examples. In addition, all the parts and% in each example are based on weight. In addition, the evaluation items in Examples and the like were measured as follows.

(1) Weight average molecular weight The molecular weight of the polymer was measured under the following conditions of the GPC (gel permeation chromatography) method.
Analyzing device: manufactured by Tosoh Corporation, HLC-8120GPC
Column: manufactured by Tosoh Corporation, G7000HXL + GMHXL + GMHXL
Column size: 7.8mmφ × 30cm each 90cm in total
Column temperature: 40 ° C
Flow rate: 0.8ml / min
Eluent: Tetrahydrofuran Detector: Differential refractometer Standard sample: Polystyrene

(2) Component ratio with molecular weight of 100,000 or less The weight fraction (Area%) with a molecular weight of 100,000 or less was calculated from the GPC measurement result of (1) above with a data processor (GPC-802, manufactured by Tosoh Corporation). At this time, the monomer component is not included.

(3) Viscosity of polymer solution The viscosity of the polymer solution was measured using a rotational viscometer under the following conditions.
Device: TBV-20H type manufactured by Toki Sangyo Co., Ltd. (with small sample adapter)
Temperature: 24 ° C ± 1 ° C
Shear rate: 25 / s
Corn rotor: NH4

(4) Gel fraction x 100
About 0.1 g of the pressure-sensitive adhesive layer immediately after the crosslinking treatment was taken and weighed to obtain the weight (W1). Next, this was wrapped in a microporous tetrafluoroethylene membrane (membrane weight W2), immersed in about 50 ml of ethyl acetate for 2 days, and then the soluble component was extracted. This was dried and the total weight (W3) was measured. From these measured values, the gel fraction (% by weight) of the pressure-sensitive adhesive layer was determined according to the following formula. Moreover, after coating, the gel fraction after storing for 1 week at room temperature was measured.
Gel fraction (% by weight) = ((W3−W2) / W1) × 100

(5) Coating property It evaluated by the viscosity of a polymer solution, the smoothness of a coating surface, the foaming state after drying, etc.
○: The coated surface is smooth and highly transparent.
X: The coated surface has streaks and is not smooth, or there are traces of ripples due to foaming.

(6) Durability Adhesive optical members cut to 12-inch size are pasted on non-alkali glass with a thickness of 0.6 mm, treated in an autoclave at 50 ° C. and 0.5 MPa for 30 minutes, and then in an atmosphere at 90 ° C. Input for 500 hours. Thereafter, the state of the adhesive optical member was visually observed and evaluated according to the following criteria.
○: There is no peeling or floating of the optical member.
X: The optical member is peeled off, floated, or foamed.

Example 1
(Preparation of acrylic polymer)
80 parts of butyl acrylate, 20 parts of 2-ethylhexyl acrylate, 5 parts of acrylic acid, 0.08 part of 2-hydroxyethyl acrylate, 0.35 part of benzoyl peroxide and 100 parts of ethyl acetate, equipped with nitrogen introduction pipe and cooling pipe Into a four-necked flask, after sufficiently purging with nitrogen, a polymerization reaction was carried out at 56 ° C. for 10 hours with stirring under a nitrogen stream, and a weight-average molecular weight of 2,200,000 and a ratio of 2% by weight of 100,000 or less. A solution of the polymer (1) was obtained. The polymerization rate was 70%, and the polymer concentration after polymerization was 36% by weight.

(Dilution of acrylic polymer)
323 parts of n-heptane (SP value 15.2 [(J / cm ³ ) ^1/2 ]) per 100 parts of polymer solid content of the acrylic polymer solution (concentration 36% by weight) is a good solvent. When 58 parts of ethyl acetate (SP value 18.6 [(J / cm ³ ) ^1/2 ]) is added, the polymer concentration becomes 16.7% by weight and the proportion of heptane in the solvent becomes 54% by weight. Since the SP value of polybutyl acrylate is 18 [(J / cm ³ ) ^1/2 ], Δδ is 2.8. The viscosity of this polymer solution was 3800 [mPa · sec].

(Manufacture of coated / dried / adhesive optical members)
To 100 parts of the polymer solid content of the acrylic polymer solution (concentration: 15% by weight), 0.1 part of 3-glycidoxypropyltrimethoxysilane as a silane coupling agent and trimethylolpropane tolylene as a crosslinking agent A pressure-sensitive adhesive composition for an optical member was prepared by uniformly mixing 0.3 part of a polyisocyanate-based crosslinking agent comprising an isocyanate adduct. Using a comma coater, it was coated on a polyethylene terephthalate film having a thickness of 38 μm subjected to silicone release treatment at a coating speed of 10 m / min so that the thickness after drying of the pressure-sensitive adhesive layer was 25 μm (drying) Corresponds to 3 minutes at 130 ° C). The said adhesive layer was transcribe | transferred to the polarizing plate and the adhesive optical member was obtained. The gel fraction of the pressure-sensitive adhesive layer was 70% by weight. The coated surface was smooth without streaks and did not foam after drying.

Example 2
(Dilution of acrylic polymer)
Polymer dilution was performed in the same manner as in Example 1 except that the acrylic polymer dilution of Example 1 was changed to 171 parts of n-heptane and 210 parts of ethyl acetate. The proportion of heptane in the solvent is 45% by weight. The viscosity of this polymer solution was 4990 [mPa · sec].

(Manufacture of coated / dried / adhesive optical members)
In the same manner as in Example 1, an adhesive optical member was obtained. The gel fraction of the pressure-sensitive adhesive layer was 71% by weight. The coated surface was smooth without streaks and did not foam after drying.

Example 3
(Dilution of acrylic polymer)
Polymer dilution was performed in the same manner as in Example 1 except that the acrylic polymer dilution of Example 1 was changed to 130 parts of n-heptane and 251 parts of ethyl acetate. The proportion of heptane in the solvent is 23% by weight. The viscosity of this polymer solution was 6500 [mPa · sec].

(Manufacture of coated / dried / adhesive optical members)
In the same manner as in Example 1, an adhesive optical member was obtained. The gel fraction of the pressure-sensitive adhesive layer was 71% by weight. The coated surface was smooth without streaks and did not foam after drying.

Example 4
(Dilution of acrylic polymer)
2,2,5 trimethylhexane (SP value 13.2 [(J / cm ³ ) ^1/2 ]) was added to 100 parts of the polymer solid content of the acrylic polymer solution (concentration 35% by weight) of Example 1. When 270 parts and 151 parts of ethyl acetate (SP value 18.6 [(J / cm ³ ) ^1/2 ]) were added, the polymer concentration became 16.7% by weight, and 2,2,5 trimethylhexane in the solvent was The ratio is 45% by weight, and since the SP value of polybutyl acrylate is 18 [(J / cm ³ ) ^1/2 ], Δδ is 4.8 The viscosity of this polymer solution is 3670 [mPa · sec. ]Met.

(Manufacture of coated / dried / adhesive optical members)
To 100 parts of the polymer solid content of the acrylic polymer solution (concentration: 15% by weight), 0.1 part of 3-glycidoxypropyltrimethoxysilane as a silane coupling agent and trimethylolpropane tolylene as a crosslinking agent A pressure-sensitive adhesive composition for an optical member was prepared by uniformly mixing 0.3 part of a polyisocyanate-based crosslinking agent comprising an isocyanate adduct. It was coated on a polyethylene terephthalate film having a thickness of 38 μm, which had been subjected to silicone release treatment using a comma coater, at a coating speed of 10 m / min so that the thickness after drying of the pressure-sensitive adhesive layer was 25 μm. Equivalent to 3 minutes at 130 ° C.). The said adhesive layer was transcribe | transferred to the polarizing plate and the adhesive optical member was obtained. The gel fraction of the pressure-sensitive adhesive layer was 72% by weight. The coated surface was smooth without streaks and did not foam after drying.

Example 5
(Dilution of acrylic polymer)
270 parts of methylcyclohexane (SP value 16.2 [(J / cm ³ ) ^1/2 ]), ethyl acetate with respect to 100 parts of polymer solids of the acrylic polymer solution (concentration 35% by weight) of Example 1 When 151 parts of (SP value 18.6 [(J / cm ³ ) ^1/2 ]) are added, the polymer concentration becomes 15% by weight and the proportion of methylcyclohexane in the solvent becomes 45% by weight. Since the SP value of polybutyl acrylate is 18 [(J / cm ³ ) ^1/2 ], Δδ is 1.8. The viscosity of this polymer solution was 3930 [mPa · sec].

(Manufacture of coated / dried / adhesive optical members)
To 100 parts of the polymer solid content of the acrylic polymer solution (concentration 15% by weight), 0.1 part of 3-glycidoxypropyltrimethoxysilane as a silane coupling agent and trimethylolpropane tolylene as a crosslinking agent A pressure-sensitive adhesive composition for an optical member was prepared by uniformly mixing 0.3 part of a polyisocyanate-based crosslinking agent comprising an isocyanate adduct. It was coated on a polyethylene terephthalate film having a thickness of 38 μm, which had been subjected to silicone release treatment using a comma coater, at a coating speed of 10 m / min so that the thickness after drying of the pressure-sensitive adhesive layer was 25 μm. Equivalent to 3 minutes at 130 ° C.). The said adhesive layer was transcribe | transferred to the polarizing plate and the adhesive optical member was obtained. The gel fraction of the pressure-sensitive adhesive layer was 69% by weight. The coated surface was smooth without streaks and did not foam after drying.

Example 6
(Preparation of acrylic polymer)
80 parts butyl acrylate, 20 parts 2-ethylhexyl acrylate, 5 parts acrylic acid. 0.08 parts of 2-hydroxyethyl acrylate, 0.35 parts of benzoyl peroxide and 120 parts of ethyl acetate were put into a four-necked flask equipped with a nitrogen introduction tube and a cooling tube, and after sufficient nitrogen substitution, While stirring under an air stream, the polymerization reaction was carried out at 55 ° C. for 10 hours, and then reacted at 70 ° C. for 2 hours. A solution of acrylic polymer (2) having a weight average molecular weight of 1,600,000 and a ratio of 14% by weight or less was obtained. The polymerization rate was 90%, and the polymer concentration after polymerization was 42% by weight.

(Dilution of acrylic polymer)
When 130 parts of n-heptane, 304 parts of acetic acid and ethyl are added to 100 parts of the polymer solid content of the acrylic polymer solution (concentration 42% by weight), the polymer concentration becomes 17.5% by weight. The proportion of heptane is 23% by weight. The viscosity of this polymer solution was 2100 [mPa · sec].

(Manufacture of coated / dried / adhesive optical members)
To 100 parts of the polymer solid content of the acrylic polymer solution (concentration: 15% by weight), 0.1 part of 3-glycidoxypropyltrimethoxysilane as a silane coupling agent and trimethylolpropane tolylene as a crosslinking agent A pressure-sensitive adhesive composition for an optical member was prepared by uniformly mixing 0.3 part of a polyisocyanate-based crosslinking agent comprising an isocyanate adduct. It was coated on a polyethylene terephthalate film having a thickness of 38 μm, which had been subjected to silicone release treatment using a comma coater, at a coating speed of 10 m / min so that the thickness after drying of the pressure-sensitive adhesive layer was 25 μm. Equivalent to 3 minutes at 130 ° C.). The said adhesive layer was transcribe | transferred to the polarizing plate and the adhesive optical member was obtained. The gel fraction of the pressure-sensitive adhesive layer was 55% by weight. The coated surface was smooth without streaks and did not foam after drying.

Example 7
(Preparation of acrylic polymer)
90 parts of butyl acrylate, 10 parts of ethyl acrylate, 1 part of acrylic acid, 0.08 part of 2-hydroxyethyl acrylate, 0.35 part of benzoyl peroxide and 100 parts of ethyl acetate, equipped with nitrogen introduction pipe and cooling pipe The mixture was placed in a four-necked flask and sufficiently purged with nitrogen, followed by a polymerization reaction at 56 ° C. for 10 hours while stirring under a nitrogen stream, and an acrylic system having a weight average molecular weight of 2.4 million and a proportion of 3% by weight of 100,000 or less. A solution of polymer (3) was obtained. The polymerization rate was 72% and the polymer concentration after polymerization was 36% by weight.

(Dilution of acrylic polymer)
255 parts of n-heptane (SP value 15.2 [(J / cm ³ ) ^1/2 ]) and ethyl acetate (SP) with respect to 100 parts of polymer solid content of the acrylic polymer solution (concentration 36% by weight). When 136 parts of the value 18.6 [(J / cm ³ ) ^1/2 ]) are added, the polymer concentration is 15% by weight and the proportion of heptane in the solvent is 45% by weight. Since the SP value of polybutyl acrylate is 18 [(J / cm ³ ) ^1/2 ], Δδ is 2.8. The viscosity of this polymer solution was 1830 [mPa · sec].

(Manufacture of coated / dried / adhesive optical members)
To 100 parts of the polymer solid content of the acrylic polymer solution (concentration: 15% by weight), 0.1 part of 3-glycidoxypropyltrimethoxysilane as a silane coupling agent and trimethylolpropane tolylene as a crosslinking agent A pressure-sensitive adhesive composition for an optical member was prepared by uniformly mixing 0.3 part of a polyisocyanate-based crosslinking agent comprising an isocyanate adduct. It was coated on a polyethylene terephthalate film having a thickness of 38 μm, which had been subjected to silicone release treatment using a comma coater, at a coating speed of 10 m / min so that the thickness after drying of the pressure-sensitive adhesive layer was 25 μm. Equivalent to 3 minutes at 130 ° C.). The said adhesive layer was transcribe | transferred to the polarizing plate and the adhesive optical member was obtained. The gel fraction of the pressure-sensitive adhesive layer was 65% by weight. The coated surface was smooth without streaks and did not foam after drying.

Comparative Example 1
(Dilution of acrylic polymer)
In the acrylic polymer dilution of Example 1, polymer dilution was performed in the same manner as in Example 1 except that ethyl acetate was changed to 381 parts without adding heptane. The viscosity of this polymer solution was 9850 [mPa · sec].

(Manufacture of coated / dried / adhesive optical members)
In the same manner as in Example 1, an adhesive optical member was obtained. The gel fraction of the pressure-sensitive adhesive layer was 73% by weight. On the coated surface, streaks occurred and a smooth surface could not be obtained.

Comparative Example 2
(Dilution of acrylic polymer)
In the acrylic polymer dilution of Example 1, the polymer dilution was performed in the same manner as in Example 1 except that n-heptane was changed to 60 parts and ethyl acetate was changed to 321 parts. The proportion of heptane in the solvent is 11% by weight. The viscosity of this polymer solution was 9080 [mPa · sec].

(Manufacture of coated / dried / adhesive optical members)
In the same manner as in Example 1, an adhesive optical member was obtained. The gel fraction of the pressure-sensitive adhesive layer was 70% by weight. On the coated surface, streaks occurred and a smooth surface could not be obtained.

Comparative Example 3
(Dilution of acrylic polymer)
Polymer dilution was performed in the same manner as in Example 1 except that in the acrylic polymer dilution of Example 1, n-heptane was changed to 381 parts. The proportion of heptane in the solvent is 67% by weight. The diluted polymer solution was cloudy and the polymer was not completely dissolved. Viscosity measurement was impossible due to the heterogeneous system.

(Preparation of coating, drying, and adhesive optical members)
In the same manner as in Example 1, an adhesive optical member was obtained. The gel fraction of the pressure-sensitive adhesive layer was 49% by weight. On the coated surface, streaks occurred and a smooth surface could not be obtained.

Comparative Example 4
(Preparation of acrylic polymer)
80 parts of butyl acrylate, 20 parts of 2-ethylhexyl acrylate, 5 parts of acrylic acid, 0.08 part of 2-hydroxyethyl acrylate, 0.35 part of benzoyl peroxide and 120 parts of ethyl acetate, equipped with nitrogen introduction tube and cooling tube The mixture was put into a four-necked flask and sufficiently purged with nitrogen, and then a polymerization reaction was carried out at 55 ° C. for 7 hours with stirring under a nitrogen stream, and then reacted at 70 ° C. for 3 hours. A solution of acrylic polymer (4) having a weight average molecular weight of 1,200,000 and a proportion of 20% by weight or less was obtained. The polymerization rate was 93%, and the polymer concentration after polymerization was 48% by weight.

(Dilution of acrylic polymer)
When 130 parts of n-heptane and 237 parts of ethyl acetate are added to 100 parts of polymer solid content of the acrylic polymer solution (concentration: 48% by weight), the polymer concentration becomes 15% by weight. The proportion is 23% by weight. The viscosity of this polymer solution was 2880 [mPa · sec].

(Manufacture of coated / dried / adhesive optical members)
Tolylene diene of trimethylolpropane as a silane coupling agent and 0.1 part of 3-glycidoxypropyltrimethoxysilane as a silane coupling agent with respect to 100 parts of polymer solid content of the above acrylic polymer solution (concentration 15% by weight) A pressure-sensitive adhesive composition for an optical member was prepared by uniformly mixing 0.8 part of a polyisocyanate-based crosslinking agent composed of an isocyanate adduct. It was coated on a polyethylene terephthalate film having a thickness of 38 μm, which had been subjected to silicone release treatment using a comma coater, at a coating speed of 10 m / min so that the thickness after drying of the pressure-sensitive adhesive layer was 25 μm. Equivalent to 3 minutes at 130 ° C.). The said adhesive layer was transcribe | transferred to the polarizing plate and the adhesive optical member was obtained. The gel fraction of the pressure-sensitive adhesive layer was 43% by weight. The coated surface was smooth without streaks and did not foam after drying.

Comparative Example 5
(Preparation of acrylic polymer)
80 parts of 2-ethylhexyl acrylate, 20 parts of butyl acrylate, 1 part of acrylic acid, 0.08 part of 2-hydroxyethyl acrylate, 0.35 part of benzoyl peroxide and 100 parts of ethyl acetate, equipped with a nitrogen introduction tube and a cooling tube The mixture was placed in a four-necked flask and sufficiently purged with nitrogen, followed by a polymerization reaction at 56 ° C. for 10 hours while stirring under a nitrogen stream, and an acrylic system having a weight average molecular weight of 2.3 million and a ratio of 4% by weight of 100,000 or less. A solution of polymer (5) was obtained. The polymerization rate was 70%, and the polymer concentration after polymerization was 35% by weight.

(Dilution of acrylic polymer)
323 parts of n-heptane (SP value 15.2 [(J / cm ³ ) ^1/2 ]) and ethyl acetate (SP) with respect to 100 parts of polymer solid content of the acrylic polymer solution (concentration 35% by weight). When 58 parts of the value 18.6 [(J / cm ³ ) ^1/2 ]) are added, the polymer concentration is 15% by weight and the proportion of heptane in the solvent is 57% by weight. Since the SP value of poly-2-ethylhexyl acrylate is 16.7 [(J / cm ³ ) ^1/2 ] calculated from the Small formula, Δδ is 1.5. P. A. Small, J. et al. Appl. Chem. 3,71 (1953) The viscosity of this polymer solution was 5120 [mPa · sec]. Moreover, the viscosity when the polymer concentration was adjusted to 15 wt% by adding only ethyl acetate without adding n-heptane was 4450 [mPa · sec], and no decrease in viscosity due to the addition of n-heptane was observed. .

以上の実施例および比較例の構成と得られた結果を表４に示す。

Table 4 shows the configurations of the above examples and comparative examples and the results obtained.

  As shown in the results of Table 4, in the method for producing a pressure-sensitive adhesive layer for an optical member of the present invention, it is possible to obtain a good coated surface with a low viscosity while reducing the amount of solvent, and the durability is also good. I understand that there is. On the other hand, in the manufacturing method of the pressure-sensitive adhesive layer for optical members of the comparative example, the viscosity is high, the coating cannot be performed uniformly, or the solution is not uniform, and it is difficult to obtain a good coated surface. I understand. Further, when the molecular weight of the acrylic polymer is lowered, the viscosity is greatly lowered, but it is apparent that the durability is deteriorated accordingly. It can also be seen that when Δδ is less than +1.7 by changing the acrylic polymer, a good viscosity reduction effect cannot be obtained.

Claims (7)

An acrylic polymer containing 60% by weight or more of an acrylic acid alkyl ester having an alkyl group having 1 to 9 carbon atoms as a monomer unit and having a weight average molecular weight of 1.5 million or more and a molecular weight of 100,000 or less. And an adhesive composition containing an organic solvent,
When the solubility parameter (SP value) of the homopolymer of the main monomer unit constituting the acrylic polymer is δ1 “(J / cm ³ ) ^1/2 ”, the difference in solubility parameter (SP value) (Δδ = δ1) A poor solvent having a solubility parameter (SP value) δ2 [(J / cm ³ ) ^1/2 ] such that −δ2) is +1.7 to +5, 20 to 60% by weight of the total amount of the organic solvent A pressure-sensitive adhesive composition.   The pressure-sensitive adhesive composition according to claim 1, wherein the acrylic polymer contains 0.2 to 7% by weight of an unsaturated carboxylic acid as a monomer unit.   The pressure-sensitive adhesive composition according to claim 1 or 2, wherein the solid content concentration is 10 to 30% by weight.   It is an adhesive layer formed by applying and drying the adhesive composition according to any one of claims 1 to 3, wherein 0.01 to 1 weight of a silane coupling agent is added to 100 parts by weight of the acrylic polymer. Part and a crosslinking agent are 0.01-5 weight part, The gel fraction after bridge | crosslinking is 45-95 weight%, The adhesive layer characterized by the above-mentioned.   The manufacturing method of an adhesive layer including the process of coating the adhesive composition in any one of Claims 1-3, and the process of drying a coated material.   A pressure-sensitive adhesive optical member, wherein the pressure-sensitive adhesive layer according to claim 4 is formed on one surface or both surfaces of the optical member.   An image display device using at least one adhesive optical member according to claim 6.