JP2009173772A - Adhesive composition for optical member, adhesive layer for optical member, adhesive optical member, and image display device - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide an adhesive composition for optical members which improves processability by shortening an aging time in crosslinking treatment, is excellent in durability even under long-term severe conditions, and forms an adhesive layer with reworkability of being capable of releasing optical members readily from liquid crystal panels without adhesive deposit. <P>SOLUTION: The adhesive composition for optical members contains (1) a (meth)acrylic polymer with a weight-average molecular weight of 500,000 or more, formed by containing as a monomer unit 50 wt% or more of an alkyl (meth)acrylate having a 4C or more alkyl group and 0.01-2 wt% of a monomer having a 4C-12C alkyl group and hydroxyl group, (2) 0.01-3 pts.wt. of a silane compound having an amino group as a silane coupling agent to 100 pts.wt. of the (meth)acrylic polymer, and (3) 0.01-2 pts.wt. of an isocyanate-based crosslinking agent to 100 pts.wt. of the (meth)acrylic polymer. <P>COPYRIGHT: (C)2009,JPO&INPIT

Description

  The present invention relates to a pressure-sensitive adhesive composition for optical members. Moreover, this invention relates to the adhesive layer for optical members formed with the said adhesive composition for optical members. Furthermore, the present invention relates to an adhesive optical member having the adhesive layer, and further to an image display device such as a liquid crystal display device, an organic EL display device and a PDP using the adhesive optical member. Examples of the optical member include a polarizing plate, a retardation plate, an optical compensation film, a brightness enhancement film, and those in which these are laminated.

  In recent years, liquid crystal display devices are widely used not only for mobile phones and personal computers but also for television applications, and the amount of materials is increasing every moment. An optical member used for the liquid crystal display device or the like, such as a polarizing plate or a retardation plate, is attached to the liquid crystal cell using an adhesive. Since the material used for such an optical member has a large expansion and contraction under a heating condition or a humidifying condition, the material is likely to float or peel off after being attached. For this reason, the pressure-sensitive adhesive for optical members is required to have durability that can cope with heating conditions and humidification conditions.

  Also, when the optical member is bonded to the liquid crystal cell, the optical member is peeled off from the liquid crystal panel and the liquid crystal cell is reused even if the bonding position is wrong or a foreign object is caught in the bonding surface. There is. When the optical member is peeled from the liquid crystal panel, it does not become an adhesive state that changes the gap of the liquid crystal cell or breaks the optical member, that is, the removability (reworkability) that can easily peel the optical member. Needed. However, when the durability of the pressure-sensitive adhesive for optical members is emphasized and the adhesiveness is simply improved, the reworkability is deteriorated.

  As the pressure-sensitive adhesive for optical members, an acrylic pressure-sensitive adhesive is generally used because of its advantages such as weather resistance and transparency. When forming the pressure-sensitive adhesive layer using an acrylic pressure-sensitive adhesive, a crosslinking treatment is usually applied in order to impart reworkability and durability. As a crosslinking method for such an acrylic pressure-sensitive adhesive, various crosslinking agents are selected and used, and a review of functional groups of the acrylic polymer as a base polymer and the crosslinking method has been published (Non-patent Document 1). ).

  Specific cross-linking agents for pressure-sensitive adhesives for optical members include isocyanate compounds, epoxy compounds, aldehyde compounds, amine compounds, metal salts, metal alkoxides, ammonium salts, hydrazine compounds, etc. (Patent Document 1), glycidyl compounds, isocyanate compounds Aziridine compounds, metal chelates and the like are also known (Patent Document 2). Moreover, although organic peroxide is illustrated as a crosslinking agent of a rubber adhesive and a silicone adhesive, it is not described as a crosslinking agent of an acrylic adhesive (nonpatent literature 2).

  In Patent Document 3, a low molecular weight acrylic polymer having a glass transition temperature of 0 to -80 ° C and a weight average molecular weight of 3 to 100,000 is used for 100 parts by weight of a high molecular weight acrylic polymer having a weight average molecular weight of 100 to 2.5 million. A pressure-sensitive adhesive composition containing 10 to 100 parts by weight and 0.001 to 10 parts by weight of a polyfunctional compound has been proposed. It is described that such an adhesive composition can prevent the occurrence of peeling, foaming and white spotting, and is excellent in reworkability. However, the pressure-sensitive adhesive composition described in Patent Document 3 also has insufficient durability and reworkability. In particular, in the case of a large-sized liquid crystal cell, gap breakage easily occurs due to insufficient reworkability.

  Patent Document 4 proposes a vulcanized natural rubber-based pressure-sensitive adhesive obtained by vulcanizing a rubber-based pressure-sensitive adhesive made of natural rubber with a silane coupling agent. Patent Document 5 proposes a pressure-sensitive adhesive containing a halogen-containing elastomer and an amino group-containing silane coupling agent. However, the pressure-sensitive adhesives described in these patent documents do not satisfy coloring weather resistance and reworkability when used in optical applications.

Adhesive Handbook (3rd edition), Adhesive Tape Industry Association, 2005, 2.3.3.2, page 31 Adhesive Handbook (Third Edition), edited by Adhesive Tape Industry Association, 2005, 2.3.6.6, page 80 JP-A-8-199131 JP 2003-49141 A JP 2002-121521 A JP 2003-96419 A JP 2006-225634 A

  The present invention can improve workability by shortening the aging time in the crosslinking treatment, has excellent durability even under long-term severe conditions, and has reworkability that allows the optical member to be easily peeled off from the liquid crystal panel without any adhesive residue. It aims at providing the adhesive composition for optical members which can form the provided adhesive layer.

  Another object of the present invention is to provide a pressure-sensitive adhesive layer formed from the pressure-sensitive adhesive composition for optical members, a pressure-sensitive adhesive optical member having the pressure-sensitive adhesive layer, and an image display device using the pressure-sensitive adhesive optical member. And

  As a result of intensive studies to solve the above problems, the present inventors have found the following pressure-sensitive adhesive composition for optical members, and have completed the present invention.

  That is, the present invention is as follows: 1) As a monomer unit, an alkyl (meth) acrylate having an alkyl group having 4 or more carbon atoms is 50% by weight or more, and a monomer having an alkyl group having 4 to 12 carbon atoms and a hydroxyl group is 0.01 to (Meth) acrylic polymer having a weight average molecular weight of 500,000 or more and 2) containing 2% by weight 2) As a silane coupling agent, an amino group-containing silane compound is added to 100 parts by weight of the (meth) acrylic polymer. 0.01 to 3 parts by weight, and 3) an adhesive composition for optical members containing 0.01 to 2 parts by weight of an isocyanate-based crosslinking agent with respect to 100 parts by weight of the (meth) acrylic polymer.

  The pressure-sensitive adhesive composition for an optical member of the present invention contains a silane compound having an amino group as a silane coupling agent and an isocyanate-based crosslinking agent. By adding specific amounts of both components, processability, durability, and reworkability can be improved.

  When the addition amount of the silane compound is less than 0.01 parts by weight, the durability of the pressure-sensitive adhesive layer is lowered during moisture storage, and peeling easily occurs. On the other hand, when it exceeds 3 weight part, the rework property of an adhesive layer falls.

  Moreover, when the addition amount of an isocyanate type crosslinking agent is less than 0.01 weight part, the elasticity modulus of an adhesive layer falls at the time of high temperature, and heat resistance falls. On the other hand, when it exceeds 2 parts by weight, the elastic modulus of the pressure-sensitive adhesive layer from room temperature to high temperature is increased, the stress relaxation property is lowered, and the warpage of the liquid crystal cell is increased.

  Moreover, durability and reworkability can be improved by making a (meth) acrylic-type polymer contain the monomer which has a C4-C12 alkyl group and a hydroxyl group as a monomer unit 0.01 to 2weight%. . When a (meth) acrylic polymer containing the monomer as a copolymerization component is used, acid-base interaction, hydrogen bond, etc. of these copolymerization components act to improve reworkability and durability, and under heating conditions It is considered that the lifting and peeling of the pressure-sensitive adhesive layer are suppressed under humidification conditions. When the content of the monomer is less than 0.01% by weight, the reactivity with the isocyanate-based crosslinking agent is poor and the durability of the pressure-sensitive adhesive layer is not improved. On the other hand, when it exceeds 2% by weight, the crosslink density becomes too high due to excessive reaction with the isocyanate-based crosslinking agent, and the stress relaxation property of the pressure-sensitive adhesive layer is lowered.

  In the pressure-sensitive adhesive composition for an optical member, it is preferable that 0.02 to 2 parts by weight of an organic peroxide is further contained with respect to 100 parts by weight of the (meth) acrylic polymer. By combining the cross-linking method using the formation of urethane bonds by the reaction of the isocyanate cross-linking agent with the hydroxyl group of the (meth) acrylic polymer and the cross-linking method using the thermal decomposition cross-linking reaction with organic peroxide, While maintaining excellent stress relaxation properties and maintaining excellent durability, it is possible to obtain excellent handling properties in the production process of the pressure-sensitive adhesive layer. When the addition amount of the organic peroxide is less than 0.02 parts by weight, the crosslinking reaction proceeds insufficiently and the durability tends to decrease. On the other hand, when the amount exceeds 2 parts by weight, the cross-linked structure is excessive, the elastic modulus of the pressure-sensitive adhesive layer is increased, the stress relaxation property is decreased, the warpage of the liquid crystal cell is increased, Uniformity tends to deteriorate.

  The amino group of the silane compound is preferably a secondary amino group. By using the silane compound which has a secondary amino group, the raise of the adhesive force of the adhesive layer after sticking to a liquid crystal cell can be suppressed.

  Moreover, it is preferable that the said isocyanate type crosslinking agent is aliphatic isocyanate from a viewpoint with a quick reaction rate.

  The (meth) acrylic polymer preferably further contains 0.01 to 2% by weight of a carboxyl group-containing monomer as a monomer unit. By including a carboxyl group-containing monomer in the (meth) acrylic polymer, durability and reworkability can be further improved. When the content of the carboxyl group-containing monomer is less than 0.01% by weight, the pressure-sensitive adhesive layer has poor crosslinking stability and tends to adversely affect durability. On the other hand, when it exceeds 2% by weight, the stress relaxation property of the pressure-sensitive adhesive layer tends to be lowered.

  Moreover, this invention relates to the adhesive layer for optical members formed by carrying out the crosslinking reaction of the adhesive composition for optical members. The pressure-sensitive adhesive layer for optical members preferably has a gel fraction of 45 to 90% by weight. The pressure-sensitive adhesive layer for optical members of the present invention is excellent in stress relaxation, durability, and reworkability. When the gel fraction of the pressure-sensitive adhesive layer for optical members is less than 45% by weight, the durability tends to decrease, and when it exceeds 90% by weight, the stress relaxation property tends to decrease.

  The present invention also relates to an adhesive optical member having the optical member pressure-sensitive adhesive layer on one or both surfaces of the optical member.

  Furthermore, the present invention relates to an image display device using at least one of the adhesive optical members.

  The pressure-sensitive adhesive composition for an optical member of the present invention is a monomer having 50% by weight or more of an alkyl (meth) acrylate having an alkyl group having 4 or more carbon atoms, and an alkyl group having 4 to 12 carbon atoms and a hydroxyl group as monomer units. (Meth) acrylic polymer having a weight average molecular weight of 500,000 or more is used as the base polymer.

  As the alkyl (meth) acrylate, an alkyl group having 4 or more carbon atoms is used. The alkyl group may be linear or branched. The alkyl group preferably has 4 to 14 carbon atoms, and more preferably 4 to 12 carbon atoms. (Meth) acrylate refers to acrylate and / or methacrylate, and (meth) of the present invention has the same meaning.

  Specific examples of the alkyl (meth) acrylate include n-butyl (meth) acrylate, s-butyl (meth) acrylate, t-butyl (meth) acrylate, isobutyl (meth) acrylate, n-pentyl (meth) acrylate, and isopentyl. (Meth) acrylate, hexyl (meth) acrylate, heptyl (meth) acrylate, isoamyl (meth) acrylate, 2-ethylhexyl (meth) acrylate, n-octyl (meth) acrylate, isooctyl (meth) acrylate, n-nonyl ( (Meth) acrylate, isononyl (meth) acrylate, n-decyl (meth) acrylate, isodecyl (meth) acrylate, n-dodecyl (meth) acrylate, isomyristyl (meth) acrylate, n-tridecyl (meth) acrylate Rate, n- tetradecyl (meth) acrylate, stearyl (meth) acrylate, isostearyl (meth) acrylate. These can be used alone or in combination.

  In the present invention, the alkyl (meth) acrylate is required to be used in an amount of 50% by weight or more based on the total monomer components of the (meth) acrylic polymer, preferably 55 to 99.99% by weight, more preferably 60 to 99.99% by weight. When the alkyl (meth) acrylate is less than 50% by weight, the adhesiveness is poor, which is not preferable.

  Examples of the monomer having an alkyl group having 4 to 12 carbon atoms and a hydroxyl group include a polymerizable functional group having an unsaturated double bond such as a (meth) acryloyl group or a vinyl group, and an alkyl having 4 to 12 carbon atoms. Those having a group and a hydroxyl group can be used without particular limitation. It is preferable that carbon number of an alkyl group is 4-8, More preferably, it is 4-6. When the carbon number of the alkyl group is 3 or less, the reactivity with the isocyanate-based crosslinking agent becomes low, and it is necessary to use a large amount of the monomer or the isocyanate-based crosslinking agent. The gel fraction of the pressure-sensitive adhesive layer becomes low and the processability deteriorates. On the other hand, the monomer having an alkyl group with 13 or more carbon atoms is difficult to obtain and is not practical.

  Examples of the monomer include 2-hydroxybutyl (meth) acrylate, 4-hydroxybutyl (meth) acrylate, 6-hydroxyhexyl (meth) acrylate, 8-hydroxyoctyl (meth) acrylate, and 10-hydroxydecyl (meth). Examples thereof include hydroxyalkyl (meth) acrylates such as acrylate and 12-hydroxylauryl (meth) acrylate; 4-hydroxymethylcyclohexyl (meth) acrylate and 4-hydroxybutyl vinyl ether. Of these, hydroxyalkyl (meth) acrylate is preferably used.

  The monomer should be used in a proportion of 0.01 to 2% by weight based on the total amount of monomer components forming the (meth) acrylic polymer. The proportion of the monomer is preferably 0.05 to 1.5% by weight, more preferably 0.1 to 1% by weight.

  As the monomer component for forming the (meth) acrylic polymer, it is preferable to use a carboxyl group-containing monomer in addition to the monomer.

  As the carboxyl group-containing monomer, a monomer having a polymerizable functional group having an unsaturated double bond such as a (meth) acryloyl group or a vinyl group and having a carboxyl group can be used without particular limitation. Examples of the carboxyl group-containing monomer include (meth) acrylic acid, carboxyethyl (meth) acrylate, carboxypentyl (meth) acrylate, itaconic acid, maleic acid, fumaric acid, and crotonic acid. These can be used alone or in combination. Among these, it is preferable to use (meth) acrylic acid, particularly acrylic acid.

  The carboxyl group-containing monomer is preferably used in a proportion of 0.01 to 2% by weight, more preferably 0.05 to 1.5% by weight, based on the total amount of monomer components forming the (meth) acrylic polymer. Particularly preferred is 0.1 to 1% by weight.

  As the monomer component for forming the (meth) acrylic polymer, other copolymerization monomers may be used alone or in combination as long as the object of the present invention is not impaired. Examples of the other copolymerizable monomer include aromatic ring-containing monomers having a polymerizable functional group having an unsaturated double bond such as a (meth) acryloyl group or a vinyl group and having an aromatic ring. . Specific examples of the aromatic ring-containing monomer include phenoxyethyl (meth) acrylate, benzyl (meth) acrylate, phenol ethylene oxide modified (meth) acrylate, 2-naphthoethyl (meth) acrylate, 2- (4-methoxy-1- And naphthoxy) ethyl (meth) acrylate, phenoxypropyl (meth) acrylate, phenoxydiethylene glycol (meth) acrylate, and polystyryl (meth) acrylate.

  In addition, acid anhydride group-containing monomers such as maleic anhydride and itaconic anhydride; caprolactone adducts of acrylic acid; styrene sulfonic acid and allyl sulfonic acid, 2- (meth) acrylamide-2-methylpropane sulfonic acid, (meth) Sulfonic acid group-containing monomers such as acrylamide propanesulfonic acid, sulfopropyl (meth) acrylate, (meth) acryloyloxynaphthalene sulfonic acid; phosphoric acid group-containing monomers such as 2-hydroxyethyl acryloyl phosphate; methoxyethyl (meth) acrylate, ( (Meth) acrylic acid alkoxyalkyl monomers such as ethoxyethyl (meth) acrylate;

  In addition, vinyl monomers such as vinyl acetate, vinyl propionate, styrene, α-methylstyrene, N-vinylcaprolactam; glycidyl (meth) acrylate, methylglycidyl (meth) acrylate, 3,4-epoxycyclohexylmethyl (meth) Epoxy group-containing monomers such as acrylate; glycol-based acrylic ester monomers such as (meth) acrylic acid polyethylene glycol, (meth) acrylic acid polypropylene glycol, (meth) acrylic acid methoxyethylene glycol, (meth) acrylic acid methoxypolypropylene glycol; Acrylic ester monomers such as tetrahydrofurfuryl (meth) acrylate, fluorine (meth) acrylate, silicone (meth) acrylate and 2-methoxyethyl acrylate; Bromide group-containing monomers, amino group-containing monomers, imide group-containing monomer, N- acryloyl morpholine, may be used, such as vinyl ether monomers.

  Furthermore, the silane type monomer containing a silicon atom etc. are mention | raise | lifted. 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 weight average molecular weight of the (meth) acrylic polymer of the present invention needs to be 500,000 or more, preferably 700,000 or more, more preferably 800,000 or more. When the weight average molecular weight is less than 500,000, the durability of the pressure-sensitive adhesive layer becomes poor, or the cohesive force of the pressure-sensitive adhesive layer becomes small and adhesive residue tends to occur. On the other hand, if the weight average molecular weight is more than 3 million, the bonding property and the adhesive strength are lowered, which is not preferable. The weight average molecular weight is a value measured by GPC (gel permeation chromatography) and calculated in terms of polystyrene.

  The production of such a (meth) acrylic polymer can be appropriately selected from known production methods such as solution polymerization, bulk polymerization, emulsion polymerization, and various radical polymerizations. Further, the (meth) acrylic polymer obtained may be any of a random copolymer, a block copolymer, a graft copolymer, and the like.

  In solution polymerization, for example, ethyl acetate, toluene or the like is used as a polymerization solvent. As a specific example of solution polymerization, the reaction is performed under an inert gas stream such as nitrogen, and a polymerization initiator is added, and the reaction is usually performed at about 50 to 70 ° C. under reaction conditions for about 5 to 30 hours.

  The polymerization initiator, chain transfer agent, emulsifier and the like used for radical polymerization are not particularly limited and can be appropriately selected and used. In addition, the weight average molecular weight of a (meth) acrylic-type polymer can be controlled by the usage-amount of a polymerization initiator and a chain transfer agent, and reaction conditions, The usage-amount is suitably adjusted according to these kinds.

  Examples of the polymerization initiator include 2,2′-azobisisobutyronitrile, 2,2′-azobis (2-amidinopropane) dihydrochloride, 2,2′-azobis [2- (5-methyl-2). -Imidazolin-2-yl) propane] dihydrochloride, 2,2'-azobis (2-methylpropionamidine) disulfate, 2,2'-azobis (N, N'-dimethyleneisobutylamidine), 2,2 '-Azobis [N- (2-carboxyethyl) -2-methylpropionamidine] hydrate (manufactured by Wako Pure Chemical Industries, VA-057) and other azo initiators, and persulfates such as potassium persulfate and ammonium persulfate , Di (2-ethylhexyl) peroxydicarbonate, di (4-t-butylcyclohexyl) peroxydicarbonate, di-sec-butyl -Oxydicarbonate, t-butylperoxyneodecanoate, t-hexylperoxypivalate, t-butylperoxypivalate, dilauroyl peroxide, di-n-octanoyl peroxide, 1,1,3 , 3-tetramethylbutylperoxy-2-ethylhexanoate, di (4-methylbenzoyl) peroxide, dibenzoyl peroxide, t-butylperoxyisobutyrate, 1,1-di (t-hexylperoxy) ) Peroxides such as cyclohexane, t-butyl hydroperoxide, hydrogen peroxide, peroxides and sodium bisulfite, peroxides and sodium ascorbate Redox initiators combined with Not intended to be.

  The polymerization initiator may be used alone or in combination of two or more, but the total content is 0.005 to 1 weight with respect to 100 parts by weight of the monomer component. The amount is preferably about 0.02 to 0.6 parts by weight.

  Examples of the chain transfer agent include lauryl mercaptan, glycidyl mercaptan, mercaptoacetic acid, 2-mercaptoethanol, thioglycolic acid, 2-ethylhexyl thioglycolate, and 2,3-dimercapto-1-propanol. The chain transfer agent may be used alone or in combination of two or more. However, the total content is 0.01 to 0 with respect to 100 parts by weight of the total amount of the monomer components. About 4 parts by weight.

  Examples of the emulsifier used in emulsion polymerization include anionic emulsifiers such as sodium lauryl sulfate, ammonium lauryl sulfate, sodium dodecylbenzenesulfonate, ammonium polyoxyethylene alkyl ether sulfate, sodium polyoxyethylene alkyl phenyl ether sulfate, and polyoxy Nonionic emulsifiers such as ethylene alkyl ether, polyoxyethylene alkyl phenyl ether, polyoxyethylene fatty acid ester, and polyoxyethylene-polyoxypropylene block polymer are listed. These may be used alone or in combination of two or more.

  Further, as reactive emulsifiers, as emulsifiers into which radical polymerizable functional groups such as propenyl groups and allyl ether groups are introduced, specifically, for example, Aqualon HS-10, HS-20, KH-10, BC-05 BC-10, BC-20 (all of which are manufactured by Daiichi Kogyo Seiyaku Co., Ltd.), Adekaria Soap SE10N (Asahi Denka Kogyo Co., Ltd.), and the like. Reactive emulsifiers are preferable because they are incorporated into the polymer chain after polymerization and thus have improved water resistance. The use amount of the emulsifier is preferably 0.3 to 5 parts by weight with respect to 100 parts by weight of the total amount of the monomer components, and more preferably 0.5 to 1 part by weight from the viewpoint of polymerization stability and mechanical stability.

  The pressure-sensitive adhesive composition for optical members of the present invention contains a silane compound having an amino group as a silane coupling agent. Examples of the silane compound include N-phenyl-3-aminopropyltrimethoxysilane, 3-aminopropyltrimethoxysilane, N-2- (aminoethyl) -3-aminopropylmethyldimethoxysilane, and 3-triethoxysilyl. -N- (1,3-dimethylbutylidene) propylamine and the like. Use of the silane compound improves the durability and reworkability of the pressure-sensitive adhesive layer. In addition, the silane compound having a secondary amino group such as N-phenyl-3-aminopropyltrimethoxysilane is more adhesive than the silane compound having a strongly basic primary amino group. It is preferably used because it can suppress an increase in adhesive strength.

  The silane compound may be used alone or in combination of two or more, but the total content is 0.01 with respect to 100 parts by weight of the (meth) acrylic polymer. It is necessary to be -3 parts by weight, preferably 0.03 to 2 parts by weight, more preferably 0.04 to 1 part by weight.

  Moreover, the adhesive composition for optical members of this invention contains an isocyanate type crosslinking agent. The isocyanate-based crosslinking agent refers to a compound having two or more isocyanate groups (including isocyanate-regenerating functional groups in which isocyanate groups are temporarily protected by blocking agents or quantification) in one molecule.

  Examples of the isocyanate-based crosslinking agent include aromatic isocyanates such as tolylene diisocyanate and xylene diisocyanate, alicyclic isocyanates such as isophorone diisocyanate, and aliphatic isocyanates such as hexamethylene diisocyanate.

  More specifically, for example, lower aliphatic polyisocyanates such as butylene diisocyanate and hexamethylene diisocyanate, alicyclic isocyanates such as cyclopentylene diisocyanate, cyclohexylene diisocyanate and isophorone diisocyanate, 2,4-tolylene diisocyanate, Aromatic diisocyanates such as 4,4′-diphenylmethane diisocyanate, xylylene diisocyanate, polymethylene polyphenyl isocyanate, trimethylolpropane / tolylene diisocyanate trimer adduct (trade name Coronate L manufactured by Nippon Polyurethane Industry Co., Ltd.), tri Methylolpropane / hexamethylene diisocyanate trimer adduct (product name: Coronate HL, manufactured by Nippon Polyurethane Industry Co., Ltd.), hexamethylene diiso Isocyanurate of anate (product name: Coronate HX, manufactured by Nippon Polyurethane Industry Co., Ltd.), polyether polyisocyanate, polyester polyisocyanate, and adducts of these with various polyols, isocyanurate bond, burette bond And polyisocyanates polyfunctionalized with allophanate bonds. Of these, it is preferable to use an aliphatic isocyanate.

  The isocyanate-based crosslinking agent may be used alone or in combination of two or more, but the total content is 100 parts by weight of the (meth) acrylic polymer. On the other hand, it is necessary to be 0.01 to 2 parts by weight, preferably 0.015 to 1 part by weight, and more preferably 0.02 to 0.8 part by weight.

  Moreover, you may use together an organic type crosslinking agent and a polyfunctional metal chelate as a crosslinking agent. Examples of the organic crosslinking agent include epoxy crosslinking agents (referring to compounds having two or more epoxy groups in one molecule). Examples of the epoxy-based crosslinking agent include ethylene glycol diglycidyl ether, propylene glycol diglycidyl ether, terephthalic acid diglycidyl ester acrylate, spiroglycol diglycidyl ether, and the like. These may be used alone or in combination of two or more.

  A polyfunctional metal chelate is one in which a polyvalent metal is covalently or coordinately bonded to an organic compound. Examples of polyvalent metal atoms include Al, Cr, Zr, Co, Cu, Fe, Ni, V, Zn, In, Ca, Mg, Mn, Y, Ce, Sr, Ba, Mo, La, Sn, Ti, and the like. can give. Examples of the atom in the organic compound that is covalently bonded or coordinated include an oxygen atom, and examples of the organic compound include an alkyl ester, an alcohol compound, a carboxylic acid compound, an ether compound, and a ketone compound.

  Moreover, it is preferable that the adhesive composition for optical members of this invention contains an organic peroxide. As the organic peroxide, one that generates radical active species by heating or light irradiation to promote the crosslinking of the base polymer of the pressure-sensitive adhesive composition can be used, but taking into consideration workability and stability, it is halved for 1 minute. It is preferable to use one having an initial temperature of 80 ° C to 160 ° C, preferably 90 ° C to 140 ° C. If the half-life temperature for 1 minute is too low, the reaction proceeds at the time of storage before coating and drying, and the viscosity may become high and the coating may become impossible. On the other hand, if the half-life temperature is too high, Since the temperature increases, side reactions occur, and a large amount of unreacted peroxide remains, which may cause crosslinking over time.

  Examples of the organic peroxide used in the present invention include di (2-ethylhexyl) peroxydicarbonate (1 minute half-life temperature: 90.6 ° C.), di (4-t-butylcyclohexyl) peroxydicarbonate. (1 minute half-life temperature: 92.1 ° C.), di-sec-butyl peroxydicarbonate (1 minute half-life temperature: 92.4 ° C.), t-butyl peroxyneodecanoate (1 minute half-life temperature : 103.5 ° C), t-hexyl peroxypivalate (half-life temperature for 1 minute: 109.1 ° C), t-butyl peroxypivalate (half-life temperature for 1 minute: 110.3 ° C), dilauroyl par Oxide (1 minute half-life temperature: 116.4 ° C.), di-n-octanoyl peroxide (1 minute half-life temperature: 117.4 ° C.), 1,1,3,3-tetramethylbutyrate Peroxy-2-ethylhexanoate (1 minute half-life temperature: 124.3 ° C), di (4-methylbenzoyl) peroxide (1 minute half-life temperature: 128.2 ° C), dibenzoyl peroxide (half-minute for 1 minute) Period temperature: 130.0 ° C.), t-butyl peroxyisobutyrate (1 minute half-life temperature: 136.1 ° C.), 1,1-di (t-hexylperoxy) cyclohexane (1 minute half-life temperature: 149.2 ° C.). In particular, di (4-t-butylcyclohexyl) peroxydicarbonate, dilauroyl peroxide, dibenzoyl peroxide, and the like are preferably used because of their excellent crosslinking reaction efficiency.

  The peroxide half-life is an index representing the decomposition rate of the peroxide, and means the time until the remaining amount of peroxide is reduced to half. The decomposition temperature for obtaining a half-life at an arbitrary time and the half-life time at an arbitrary temperature are described in the manufacturer catalog, for example, “Organic peroxide catalog 9th edition by Nippon Oil & Fats Co., Ltd.” (May 2003) ".

  The organic peroxide may be used alone or as a mixture of two or more, but the total content is 100 parts by weight of the (meth) acrylic polymer. It is preferable that it is 0.02-2 weight part with respect to it, More preferably, it is 0.05-1 weight part, More preferably, it is 0.08-0.6 weight part.

  In the production of the pressure-sensitive adhesive layer, it is preferable to adjust the addition amount of the cross-linking agent so that the gel fraction of the cross-linked pressure-sensitive adhesive layer is 45 to 90% by weight, more preferably 47 to 85% by weight. More preferably, it is 50 to 80% by weight.

  The predetermined gel fraction can be adjusted by adjusting the addition amount of a crosslinking agent, a peroxide, etc., and considering the influence of the crosslinking treatment temperature and the crosslinking treatment time. The adjustment of the crosslinking treatment temperature and the crosslinking treatment time is preferably set, for example, so that the decomposition amount of peroxide contained in the pressure-sensitive adhesive composition for optical members is 75% by weight or more, more preferably 80% by weight. As mentioned above, More preferably, it is 85 weight% or more. When the amount of peroxide decomposition is less than 75% by weight, the amount of peroxide remaining in the pressure-sensitive adhesive composition for optical members increases, and as a result, a cross-linking reaction occurs over time even after heat treatment. In some cases, the gel fraction exceeds 90% by weight, which is not preferable.

  More specifically, for example, when the heat treatment temperature is 1 minute half-life temperature, the decomposition amount of peroxide is 50% by weight in 1 minute, and the decomposition amount of peroxide is 75% by weight in 2 minutes. A heat treatment time of 2 minutes or more is required. For example, if the half-life of the peroxide at the heat treatment temperature (half time) is 30 seconds, a heat treatment time of 1 minute or more is required, and for example, the half-life of the peroxide at the crosslinking treatment temperature Is 5 minutes, a crosslinking treatment time of 10 minutes or more is required.

  In this way, the crosslinking treatment temperature and crosslinking treatment time can be calculated by theoretical calculation from the half-life, assuming that the peroxide is linearly proportional, depending on the peroxide used, and the addition amount should be adjusted appropriately. Can do. On the other hand, the higher the temperature, the higher the possibility of side reactions, so the crosslinking treatment temperature is preferably 170 ° C. or lower.

  The cross-linking treatment may be performed at the temperature during the drying step of the pressure-sensitive adhesive layer, or may be performed by providing a separate cross-linking treatment step after the drying step. However, the temperature of the optical member increases and the characteristics of the optical member change. Since there is a case, it is desirable to carry out before bonding to an optical member.

  The crosslinking treatment time can be set in consideration of productivity and workability, but is usually about 0.2 to 20 minutes, and preferably about 0.5 to 10 minutes.

  The pressure-sensitive adhesive composition for optical members of the present invention may contain other known additives, such as powders such as colorants and pigments, dyes, surfactants, plasticizers, and tackifiers. Agents, surface lubricants, leveling agents, softeners, antioxidants, anti-aging agents, light stabilizers, UV absorbers, polymerization inhibitors, inorganic or organic fillers, metal powders, particles, foils, etc. It can add suitably according to the use to be used. At that time, it is necessary to adjust the addition amount to such an extent that the elastic modulus of the pressure-sensitive adhesive layer is not significantly changed.

  The pressure-sensitive adhesive optical member of the present invention is obtained by forming a pressure-sensitive adhesive layer with the pressure-sensitive adhesive composition on at least one surface of an optical member.

  As a method for forming the pressure-sensitive adhesive layer, for example, a method in which the pressure-sensitive adhesive composition is applied to a release-processed separator, the polymerization solvent is dried and removed to form a pressure-sensitive adhesive layer, and then transferred to an optical member, or The pressure-sensitive adhesive composition is prepared by applying the pressure-sensitive adhesive composition to an optical member, drying and removing a polymerization solvent, and the like to form a pressure-sensitive adhesive layer on the optical member. In applying the pressure-sensitive adhesive, one or more solvents other than the polymerization solvent may be added as appropriate.

  In addition, the pressure-sensitive adhesive layer can be formed after forming an anchor layer on the surface of the optical member or performing various easy adhesion treatments such as corona treatment and plasma treatment. Moreover, you may perform an easily bonding process on the surface of an adhesive layer.

  Various methods are used as a method of forming the pressure-sensitive adhesive layer. Specifically, for example, roll coat, kiss roll coat, gravure coat, reverse coat, roll brush, spray coat, dip roll coat, bar coat, knife coat, air knife coat, curtain coat, lip coat, die coater, etc. Examples thereof include an extrusion coating method.

  The thickness of the pressure-sensitive adhesive layer after drying is not particularly limited, and is, for example, about 2 to 500 μm, preferably 5 to 100 μm.

  When the pressure-sensitive adhesive layer is exposed, the pressure-sensitive adhesive layer may be protected with a sheet (separator) that has been subjected to a release treatment until practical use.

  Examples of the constituent material of the separator include, for example, plastic films such as polyethylene, polypropylene, polyethylene terephthalate, and polyester films, porous materials such as paper, cloth, and nonwoven fabric, nets, foam sheets, metal foils, and laminates thereof. A thin film can be used, but a plastic film is preferably used because of its excellent surface smoothness.

  The plastic film is not particularly limited as long as it can protect the pressure-sensitive adhesive layer. For example, polyethylene film, polypropylene film, polybutene film, polybutadiene film, polymethylpentene film, polyvinyl chloride film, vinyl chloride copolymer Examples thereof include a coalesced film, a polyethylene terephthalate film, a polybutylene terephthalate film, a polyurethane film, and an ethylene-vinyl acetate copolymer film.

  The thickness of the separator is usually about 5 to 200 μm, preferably about 10 to 100 μm. For the separator, if necessary, mold release and antifouling treatment with a silicone type, fluorine type, long chain alkyl type or fatty acid amide type release agent, silica powder, etc., coating type, kneading type, vapor deposition type It is also possible to carry out antistatic treatment such as. In particular, when the surface of the separator is appropriately subjected to a release treatment such as silicone treatment, long-chain alkyl treatment, or fluorine treatment, the peelability from the pressure-sensitive adhesive layer can be further improved.

  In addition, the sheet | seat which carried out the peeling process used for preparation of said adhesive type optical member can be used as a separator of an adhesive type optical member as it is, and can simplify in a process surface.

  As the optical member, those used for forming an image display device such as a liquid crystal display device are 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 polarizers include dichroic iodine and dichroic dyes on hydrophilic polymer films such as polyvinyl alcohol films, partially formalized polyvinyl alcohol films, and ethylene / vinyl acetate copolymer partially saponified films. Examples thereof include polyene-based oriented films such as those obtained by adsorbing 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 prepared, for example, by immersing 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 or 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, may be performed while dyeing, or may be dyed with iodine after stretching. The film can be stretched even in an aqueous solution such as boric acid or potassium iodide or in a water bath.

  As a material constituting the transparent protective film, for example, a thermoplastic resin excellent in transparency, mechanical strength, thermal stability, moisture barrier property, isotropy and the like is used. Specific examples of such thermoplastic resins include cellulose resins such as triacetyl cellulose, polyester resins, polyethersulfone resins, polysulfone resins, polycarbonate resins, polyamide resins, polyimide resins, polyolefin resins, (meth) acrylic resins, cyclic Examples thereof include polyolefin resins (norbornene resins), polyarylate resins, polystyrene resins, polyvinyl alcohol resins, and mixtures thereof. A transparent protective film is bonded to one side of the polarizer by an adhesive layer. On the other side, as a transparent protective film, (meth) acrylic, urethane-based, acrylurethane-based, epoxy-based, silicone A thermosetting resin such as a system or an ultraviolet curable resin can be used. One or more kinds of arbitrary appropriate additives may be contained in the transparent protective film. Examples of the additive include an ultraviolet absorber, an antioxidant, a lubricant, a plasticizer, a mold release agent, an anti-coloring agent, a flame retardant, a nucleating agent, an antistatic agent, a pigment, and a coloring agent. The content of the thermoplastic resin in the transparent protective film is preferably 50 to 100% by weight, more preferably 50 to 99% by weight, still more preferably 60 to 98% by weight, and particularly preferably 70 to 97% by weight. . When content of the said thermoplastic resin in a transparent protective film is 50 weight% or less, there exists a possibility that the high transparency etc. which a thermoplastic resin originally has cannot fully be expressed.

  Moreover, as a transparent protective film, the polymer film as described in Unexamined-Japanese-Patent No. 2001-343529 (WO01 / 37007), for example, (A) thermoplastic resin which has a substituted and / or unsubstituted imide group in a side chain, ( B) Resin compositions containing thermoplastic resins having substituted and / or unsubstituted phenyl and nitrile groups in the side chains. 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. Since these films have a small phase difference and a small photoelastic coefficient, problems such as unevenness due to the distortion of the polarizing plate can be eliminated, and since the moisture permeability is small, the humidification durability is excellent.

  Although the thickness of a transparent 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. The transparent protective film is particularly suitable when the thickness is 5 to 150 μm.

  In addition, when providing a transparent protective film on 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.

  As the transparent protective film, it is preferable to use at least one selected from cellulose resin, polycarbonate resin, cyclic polyolefin resin, and (meth) acrylic resin.

  Cellulose resin is an ester of cellulose and fatty acid. Specific examples of the cellulose ester resin include triacetyl cellulose, diacetyl cellulose, tripropionyl cellulose, dipropionyl cellulose and the like. Among these, triacetyl cellulose is particularly preferable. Many products of triacetylcellulose are commercially available, which is advantageous in terms of availability and cost. Examples of commercially available products of triacetyl cellulose include trade names “UV-50”, “UV-80”, “SH-80”, “TD-80U”, “TD-TAC”, and “UZ” manufactured by Fujifilm Corporation. -TAC "and" KC series "manufactured by Konica. In general, these triacetyl celluloses have an in-plane retardation (Re) of almost zero, but a thickness direction retardation (Rth) of about 60 nm.

  In addition, the cellulose resin film with a small thickness direction phase difference is obtained by processing the said cellulose resin, for example. For example, a base film such as polyethylene terephthalate, polypropylene, and stainless steel coated with a solvent such as cyclopentanone and methyl ethyl ketone is bonded to a general cellulose film and dried by heating (for example, at 80 to 150 ° C. for about 3 to 10 minutes). ) And then peeling the base film; a solution obtained by dissolving norbornene resin, (meth) acrylic resin, etc. in a solvent such as cyclopentanone, methyl ethyl ketone, etc. is applied to a general cellulose resin film and dried by heating ( For example, a method of peeling the coated film after 80 to 150 ° C. for about 3 to 10 minutes is mentioned.

  Moreover, as a cellulose resin film with a small thickness direction retardation, the fatty acid cellulose resin film which controlled the fat substitution degree can be used. Generally used triacetyl cellulose has an acetic acid substitution degree of about 2.8. Preferably, the Rth can be reduced by controlling the acetic acid substitution degree to 1.8 to 2.7. Rth can be controlled to be small by adding a plasticizer such as dibutyl phthalate, p-toluenesulfonanilide, acetyltriethyl citrate to the fatty acid-substituted cellulose resin. The addition amount of the plasticizer is preferably 40 parts by weight or less, more preferably 1 to 20 parts by weight, and still more preferably 1 to 15 parts by weight with respect to 100 parts by weight of the fatty acid cellulose resin.

  Specific examples of the cyclic polyolefin resin are preferably norbornene resins. The cyclic olefin-based resin is a general term for resins that are polymerized using a cyclic olefin as a polymerization unit, and is described in, for example, JP-A-1-240517, JP-A-3-14882, JP-A-3-122137, and the like. Resin. Specific examples include ring-opening (co) polymers of cyclic olefins, addition polymers of cyclic olefins, cyclic olefins and α-olefins such as ethylene and propylene (typically random copolymers), And graft polymers obtained by modifying them with an unsaturated carboxylic acid or a derivative thereof, and hydrides thereof. Specific examples of the cyclic olefin include norbornene monomers.

  Various products are commercially available as the cyclic polyolefin resin. As specific examples, trade names “ZEONEX” and “ZEONOR” manufactured by ZEON CORPORATION, product names “ARTON” manufactured by JSR Corporation, “TOPAS” manufactured by TICONA, and product names manufactured by Mitsui Chemicals, Inc. “APEL”.

  The (meth) acrylic resin preferably has a Tg (glass transition temperature) of 115 ° C. or higher, more preferably 120 ° C. or higher, still more preferably 125 ° C. or higher, and particularly preferably 130 ° C. or higher. When Tg is 115 ° C. or higher, the polarizing plate can be excellent in durability. Although the upper limit of Tg of the (meth) acrylic resin is not particularly limited, it is preferably 170 ° C. or lower from the viewpoint of moldability and the like. From the (meth) acrylic resin, a film having in-plane retardation (Re) and thickness direction retardation (Rth) of almost zero can be obtained.

  As the (meth) acrylic resin, any appropriate (meth) acrylic resin can be adopted as long as the effects of the present invention are not impaired. For example, poly (meth) acrylic acid ester such as polymethyl methacrylate, methyl methacrylate- (meth) acrylic acid copolymer, methyl methacrylate- (meth) acrylic acid ester copolymer, methyl methacrylate-acrylic acid ester- (Meth) acrylic acid copolymer, (meth) methyl acrylate-styrene copolymer (MS resin, etc.), polymer having an alicyclic hydrocarbon group (for example, methyl methacrylate-cyclohexyl methacrylate copolymer, Methyl methacrylate- (meth) acrylate norbornyl copolymer, etc.). Preferably, poly (meth) acrylate C1-6 alkyl such as poly (meth) acrylate methyl is used. More preferred is a methyl methacrylate resin containing methyl methacrylate as a main component (50 to 100% by weight, preferably 70 to 100% by weight).

  Specific examples of (meth) acrylic resins include (meth) acrylic resins having a ring structure in the molecule described in, for example, Acrypet VH and Acrypet VRL20A manufactured by Mitsubishi Rayon Co., Ltd., and JP-A-2004-70296. And a high Tg (meth) acrylic resin system obtained by intramolecular crosslinking or intramolecular cyclization reaction.

  A (meth) acrylic resin having a lactone ring structure can also be used as the (meth) acrylic resin. It is because it has high mechanical strength by high heat resistance, high transparency, and biaxial stretching.

  Examples of the (meth) acrylic resin having a lactone ring structure include JP 2000-230016, JP 2001-151814, JP 2002-120326, JP 2002-254544, and JP 2005. Examples thereof include (meth) acrylic resins having a lactone ring structure described in Japanese Patent No. 146084.

  The (meth) acrylic resin having a lactone ring structure preferably has a ring pseudo structure represented by the following general formula (Formula 1).

^Wherein, R 1, ^{R 2} and ^{R 3} each independently represent a hydrogen atom or an organic residue having 1 to 20 carbon atoms. The organic residue may contain an oxygen atom.

  The content ratio of the lactone ring structure represented by the general formula (Formula 1) in the structure of the (meth) acrylic resin having a lactone ring structure is preferably 5 to 90% by weight, more preferably 10 to 70% by weight, More preferably, it is 10 to 60% by weight, and particularly preferably 10 to 50% by weight. When the content of the lactone ring structure represented by the general formula (Chemical Formula 1) in the structure of the (meth) acrylic resin having a lactone ring structure is less than 5% by weight, the heat resistance, solvent resistance, and surface hardness are low. May be insufficient. If the content of the lactone ring structure represented by the general formula (Chemical Formula 1) in the structure of the (meth) acrylic resin having a lactone ring structure is more than 90% by weight, molding processability may be poor.

  The (meth) acrylic resin having a lactone ring structure has a mass average molecular weight (sometimes referred to as a weight average molecular weight) of preferably 1,000 to 2,000,000, more preferably 5,000 to 1,000,000, still more preferably 10,000 to 500,000, and particularly preferably. Is 50,000 to 500,000. If the mass average molecular weight is out of the above range, it is not preferable from the viewpoint of molding processability.

  The (meth) acrylic resin having a lactone ring structure preferably has a Tg of 115 ° C. or higher, more preferably 120 ° C. or higher, still more preferably 125 ° C. or higher, and particularly preferably 130 ° C. or higher. Since Tg is 115 ° C. or higher, for example, when incorporated into a polarizing plate as a transparent protective film, it has excellent durability. Although the upper limit of Tg of the (meth) acrylic resin having the lactone ring structure is not particularly limited, it is preferably 170 ° C. or less from the viewpoint of moldability and the like.

  The (meth) acrylic resin having a lactone ring structure is preferably as the total light transmittance of a molded product obtained by injection molding measured by a method according to ASTM-D-1003 is higher, preferably 85. % Or more, more preferably 88% or more, and still more preferably 90% or more. The total light transmittance is a measure of transparency. If the total light transmittance is less than 85%, the transparency may be lowered.

  As the transparent protective film, one having a front phase difference of less than 40 nm and a thickness direction retardation of less than 80 nm is usually used. The front phase difference Re is represented by Re = (nx−ny) × d. The thickness direction retardation Rth is represented by Rth = (nx−nz) × d. The Nz coefficient is represented by Nz = (nx−nz) / (nx−ny). [However, the refractive indexes in the slow axis direction, the fast axis direction, and the thickness direction of the film are nx, ny, and nz, respectively, and d (nm) is the thickness of the film. The slow axis direction is the direction that maximizes the refractive index in the film plane. ]. In addition, it is preferable that a transparent protective film has as little color as possible. A protective film having a thickness direction retardation value 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 transparent 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.

  On the other hand, as the transparent protective film, a phase difference plate having a phase difference with a front phase difference of 40 nm or more and / or a thickness direction retardation of 80 nm or more can be used. The front phase difference is usually controlled in the range of 40 to 200 nm, and the thickness direction phase difference is usually controlled in the range of 80 to 300 nm. When a retardation plate is used as the transparent protective film, the retardation plate functions also as a transparent protective film, so that the thickness can be reduced.

  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, polyamide, polyimide, polyolefin, polyvinyl chloride, cellulose resin, cyclic polyolefin resin (norbornene resin), or any of these binary, ternary copolymers, graft copolymers Examples thereof include polymers and blends. These polymer materials become an oriented product (stretched film) by stretching or the like.

  Examples of the liquid crystal 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. . Specific examples of the main chain type liquid crystal polymer include a nematic alignment polyester liquid crystal polymer, a discotic polymer, and a cholesteric polymer having a structure in which a mesogen group is bonded at a spacer portion that imparts flexibility. Specific examples of the side chain type liquid crystal polymer include polysiloxane, polyacrylate, polymethacrylate, or polymalonate as a main chain skeleton, and a nematic alignment-providing para-substitution through a spacer portion composed of a conjugated atomic group as a side chain. Examples thereof include those having a mesogenic part composed of a cyclic compound unit. These liquid crystal polymers can be prepared by, for example, applying a solution of a liquid crystalline polymer on an alignment surface such as a surface of a thin film such as polyimide or polyvinyl alcohol formed on a glass plate, or an oblique deposition of 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. It may be one in which retardation plates are stacked and optical characteristics such as retardation are controlled.

  The retardation plate has a relationship of nx = ny> nz, nx> ny> nz, nx> ny = nz, nx> nz> ny, nz = nx> ny, nz> nx> ny, nz> nx = ny. What is satisfactory is selected and used according to various applications. Note that ny = nz includes not only the case where ny and nz are completely the same, but also the case where ny and nz are substantially the same.

  For example, in a phase difference plate that satisfies nx> ny> nz, a surface plate having a front phase difference of 40 to 100 nm, a thickness direction phase difference of 100 to 320 nm, and an Nz coefficient of 1.8 to 4.5 is used. Is preferred. For example, in a retardation plate (positive A plate) that satisfies nx> ny = nz, it is preferable to use a retardation plate that satisfies a front phase difference of 100 to 200 nm. For example, for a retardation plate (negative A plate) that satisfies nz = nx> ny, it is preferable to use a retardation plate that satisfies a front phase difference of 100 to 200 nm. For example, in a retardation plate satisfying nx> nz> ny, it is preferable to use a retardation plate having a front phase difference of 150 to 300 nm and an Nz coefficient exceeding 0 to 0.7. As described above, for example, a material satisfying nx = ny> nz, nz> nx> ny, or nz> nx = ny can be used.

  The transparent protective film can be appropriately selected according to the applied liquid crystal display device. For example, in the case of VA (including Vertical Alignment, MVA, and PVA), it is desirable that at least one of the polarizing plates (cell side) has a retardation. As specific phase differences, it is desirable that Re = 0 to 240 nm and Rth = 0 to 500 nm. In terms of the three-dimensional refractive index, nx> ny = nz, nx> ny> nz, nx> nz> ny, nx = ny> nz (positive A plate, biaxial, negative C plate) are desirable. In the VA type, it is preferable to use a combination of a positive A plate and a negative C plate, or one biaxial film. When polarizing plates are used above and below the liquid crystal cell, both the upper and lower sides of the liquid crystal cell may have a phase difference, or any one of the upper and lower transparent protective films may have a phase difference.

  For example, in the case of IPS (including In-Plane Switching, FFS), both cases where the transparent protective film on one side of the polarizing plate has a phase difference and does not have a phase difference can be used. For example, when there is no phase difference, it is desirable that the liquid crystal cell does not have a phase difference both above and below (cell side). In the case where the liquid crystal cell has a phase difference, it is desirable that the liquid crystal cell has a phase difference in the upper and lower sides, or the upper and lower sides have a phase difference (for example, nx> nz> ny on the upper side). Biaxial film satisfying the relationship, when there is no retardation on the lower side, positive A plate on the upper side, and positive C plate on the lower side). When it has a phase difference, it is desirable that Re = −500 to 500 nm and Rth = −500 to 500 nm. In terms of the three-dimensional refractive index, nx> ny = nz, nx> nz> ny, nz> nx = ny, nz> nx> ny (positive A plate, biaxial, positive C plate) are desirable.

  In addition, the film which has the said phase difference can be separately bonded to the transparent protective film which does not have a phase difference, and the said function can be provided.

  The transparent protective film may be subjected to surface modification treatment in order to improve adhesiveness with the polarizer before applying the adhesive. Specific examples of the treatment include corona treatment, plasma treatment, flame treatment, ozone treatment, primer treatment, glow treatment, saponification treatment, and treatment with a coupling agent. Further, an antistatic layer can be appropriately formed.

  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.

  The 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 is used. 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. In addition, the sticking prevention treatment is performed for the purpose of preventing adhesion with an adjacent layer (for example, a backlight-side diffusion plate).

  The anti-glare treatment is applied for the purpose of preventing the outside light from being reflected on the surface of the polarizing plate and obstructing the visibility of the light transmitted through the polarizing plate. For example, the surface is roughened by 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. Examples of the fine particles to be included in the formation of the surface fine concavo-convex structure include conductive materials made of silica, alumina, titania, zirconia, tin oxide, indium oxide, cadmium oxide, antimony oxide, and the like having an average particle diameter of 0.5 to 20 μm. In some cases, transparent fine particles such as inorganic fine particles, organic fine particles composed of a crosslinked or uncrosslinked polymer, and the like are used. When forming the surface fine uneven structure, the amount of fine particles used is generally about 2 to 70 parts by weight, preferably 5 to 50 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.

  An adhesive is used for the adhesion treatment between the polarizer and the transparent protective film. Examples of the adhesive include isocyanate adhesives, polyvinyl alcohol adhesives, gelatin adhesives, vinyl latexes, and water-based polyesters. The said adhesive agent is normally used as an adhesive agent which consists of aqueous solution, and contains 0.5 to 60 weight% of solid content normally. In addition to the above, examples of the adhesive between the polarizer and the transparent protective film include an ultraviolet curable adhesive and an electron beam curable adhesive. The electron beam curable polarizing plate adhesive exhibits suitable adhesion to the various transparent protective films. The adhesive used in the present invention can contain a metal compound filler.

  In addition, as an optical member, for example, for forming a liquid crystal display device such as a reflection plate, an anti-transmission plate, the retardation plate (including wavelength plates such as 1/2 and 1/4), a visual compensation film, and a brightness enhancement film. The optical layer which may be used is mentioned. These can be used alone as an optical member, or can be laminated on the polarizing plate for practical use and used as one layer or two or more layers.

  In particular, a reflective polarizing plate or a 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 a 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 visual compensation film is further laminated on a plate, or a polarizing plate in which a luminance 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. In addition, the transparent protective film may contain fine particles to form 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. Moreover, the 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 of the fine concavo-convex structure reflecting the surface fine concavo-convex structure of the transparent protective film is formed by, for example, applying metal to the surface of the transparent protective layer by an appropriate method such as a vacuum deposition method, an ion plating method, a sputtering method, or a plating method. It can be performed by a method of attaching directly to the screen.

  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 of a type that displays an image using a built-in power 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 can be used to form liquid crystal display devices that can save energy when using a light source such as a backlight in a bright atmosphere and can be used with a built-in power supply 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 an image is displayed in color, and also has an antireflection function.

  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 visual 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. Examples of such a visual compensation phase difference plate include a phase difference plate, an alignment film such as a liquid crystal polymer, and a film in which an alignment layer such as a liquid crystal polymer is supported on a transparent substrate. A normal retardation plate uses a birefringent polymer film that is uniaxially stretched in the plane direction, whereas a retardation plate used as a visual compensation film is biaxially stretched 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, and 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.

  In addition, from the viewpoint of achieving a wide viewing angle with good visibility, an optical compensation position in which an alignment layer of a liquid crystal polymer, particularly an optically anisotropic layer composed of a tilted alignment layer of a discotic liquid crystal polymer, is supported by a triacetyl cellulose film. A phase difference 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 or the like provided behind the brightness enhancement film and re-incident on the brightness enhancement film, and part or all of the light is transmitted as light having 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 accordingly, the amount of light that can be used for liquid crystal image display or the like is reduced and the image becomes dark. The brightness enhancement film reflects light that has a polarization direction that is absorbed by the polarizer without being incident on the polarizer, and is reflected by the brightness enhancement film, and then inverted through a reflective layer or the like provided behind the brightness enhancement film. The brightness enhancement film transmits only the polarized light in which the polarization direction of the light reflected and inverted between the two is allowed to pass through the polarizer. Since the light is supplied to the polarizer, 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 light in the natural light state is directed toward the reflection layer or the like, reflected through the reflection layer or the like, and again passes through the diffusion plate and reenters the brightness enhancement film. In this way, by providing a diffuser plate that returns polarized light to the original natural light between the brightness enhancement film and the reflective layer, the brightness of the display screen is maintained, and at the same time, the brightness of the display screen is reduced and uniform. Can provide a bright screen. 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 material or a multilayer laminate of thin film films having different refractive index anisotropies. 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 transmits circularly polarized light such as a cholesteric liquid crystal layer, it can be incident on a polarizer as it is, but from the point of suppressing absorption loss, the circularly polarized light is converted into linearly polarized light through a retardation plate. It is preferably incident on the 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 at a wide wavelength in the visible light region or the like exhibits, for example, a retardation plate that functions as a quarter-wave plate for light light having a wavelength of 550 nm and other retardation characteristics. It can be obtained by a method in which a phase difference layer, for example, a phase difference layer that functions as a half-wave plate is superimposed. 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, a cholesteric liquid crystal layer having a reflection structure that reflects circularly polarized light in a wide wavelength range such as a visible light range can be obtained by combining two or more layers with different reflection wavelengths to form 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 more optical layers as in 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-described reflective polarizing plate or semi-transmissive 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 a liquid crystal display device or the like can be improved because of excellent stability and assembly work. 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 adhesive type optical member is used, and the conventional method can be applied. As the liquid crystal cell, an arbitrary type such as an arbitrary type such as a TN type, STN type, π type, VA type, or IPS 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. The optical member (polarizing plate or the like) of the present invention can also be applied to an organic EL display device. 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 with reference to examples, but the present invention is not limited to these examples. In addition, all the parts and% in each example are based on weight.
Evaluation items in Examples and the like were measured as follows.

<Measurement of weight average molecular weight>
The weight average molecular weight of the obtained (meth) acrylic polymer was measured by GPC (gel permeation chromatography). The sample used was a filtrate obtained by dissolving the sample in tetrahydrofuran to make a solution of about 0.1% by weight, which was allowed to stand overnight, and then filtered through a 0.45 μm membrane filter.
Analyzing device: manufactured by Tosoh Corporation, HLC-8120GPC
Column: manufactured by Tosoh Corporation, G7000H _XL -H + GMH _XL -H + GMH _XL
Column size: 7.8mmφ × 30cm each 90cm in total
Column temperature: 40 ° C
Flow rate: 0.8mL / min
Eluent: Tetrahydrofuran solution concentration: about 0.1% by weight
Injection volume: 100 μL
Detector: Differential refractometer (RI)
Standard sample: Polystyrene data processor: GPC-8020, manufactured by Tosoh Corporation

<Measurement of gel fraction>
About 0.1 g of the pressure-sensitive adhesive layer immediately after the crosslinking treatment was taken and weighed to determine the weight (W ₁ ). Next, this was wrapped in a microporous tetrafluoroethylene membrane (membrane weight W ₂ ), immersed in about 50 ml of ethyl acetate at 23 ° C. for 2 days, and then the soluble component was extracted. Then removed the adhesive layer with the film, which was dried for 2 hours at 120 ° C., was measured total weight (W _3). The gel fraction (% by weight) of the pressure-sensitive adhesive layer was determined from these measured values according to the following formula. Moreover, the gel fraction of the adhesive layer after storing for 1 week at room temperature after coating was measured.
Gel fraction = [(W ₃ −W ₂ ) / W ₁ ] × 100

Example 1
(Preparation of acrylic polymer A)
In a four-necked flask equipped with a stirring blade, thermometer, nitrogen gas inlet tube, and condenser, 50 parts of butyl acrylate, 50 parts of 2-ethylhexyl acrylate, 0.3 part of 4-hydroxybutyl acrylate, 0.3 part of acrylic acid Then, 0.1 part of 2,2′-azobisisobutyronitrile (manufactured by Wako Pure Chemical Industries, Ltd.) as a polymerization initiator was charged together with 200 parts of ethyl acetate, sufficiently purged with nitrogen, and then stirred while stirring under a nitrogen stream. A polymerization reaction was carried out for 9 hours while keeping the liquid temperature around 60 ° C. to prepare an acrylic polymer A solution. The resulting acrylic polymer A had a weight average molecular weight of 1,630,000.

(Preparation of adhesive composition)
0.1 part of N-phenyl-3-aminopropyltrimethoxysilane (manufactured by Shin-Etsu Silicone, KBM573) as a silane coupling agent with respect to 100 parts of the solid content of the acrylic polymer A solution, hexamethylene diisocyanate of trimethylolpropane 0.15 parts of an adduct (D-160N, manufactured by Mitsui Takeda Chemical Co., Ltd.) was added, and the mixture was uniformly mixed and stirred to prepare an adhesive composition 1.

(Preparation of polarizing plate with adhesive layer)
The pressure-sensitive adhesive composition 1 was applied to one side of a silicone-treated polyethylene terephthalate (PET) film (manufactured by Toray Industries, Inc., thickness: 38 μm), heated at 130 ° C. for 3 minutes, and dried to a thickness of 25 μm. An adhesive layer was formed. The gel fraction of the pressure-sensitive adhesive layer immediately after drying was 45% by weight. Next, the pressure-sensitive adhesive layer was bonded to a polarizing plate and transferred to prepare a polarizing plate with a pressure-sensitive adhesive layer. In addition, the gel fraction after aging of an adhesive layer was 66 weight%.

Example 2
(Preparation of adhesive composition)
For 100 parts of the solid content of the acrylic polymer A solution, 0.1 part of N-phenyl-3-aminopropyltrimethoxysilane (KBM573) as a silane coupling agent, dibenzoyl peroxide (one minute half-life 130 ° C.) 0.2 parts (manufactured by Wako Pure Chemical Industries, Ltd.) and 0.05 parts of a trimethylolpropane hexamethylene diisocyanate adduct (D-160N) were added and mixed uniformly and stirred to prepare an adhesive composition 2.

(Preparation of polarizing plate with adhesive layer)
The pressure-sensitive adhesive composition 2 was applied to one side of a silicone-treated PET film (Toray Industries, Inc., thickness: 38 μm) and heated at 130 ° C. for 3 minutes. About 88%) A pressure-sensitive adhesive layer having a thickness of 25 μm after drying was formed. The gel fraction of the pressure-sensitive adhesive layer immediately after drying was 59% by weight. Next, the pressure-sensitive adhesive layer was bonded to a polarizing plate and transferred to prepare a polarizing plate with a pressure-sensitive adhesive layer. In addition, the gel fraction after aging of an adhesive layer was 64 weight%.

Example 3
(Preparation of adhesive composition)
As a silane coupling agent, 0.05 part of N-phenyl-3-aminopropyltrimethoxysilane (KBM573), dibenzoyl peroxide (manufactured by Wako Pure Chemical Industries) 3 parts, 0.02 part of trimethylolpropane hexamethylene diisocyanate adduct (D-160N) was added, and the mixture was uniformly mixed and stirred to prepare an adhesive composition 3.

(Preparation of polarizing plate with adhesive layer)
The pressure-sensitive adhesive composition 3 was applied on one side of a silicone-treated PET film (manufactured by Toray Industries, Inc., thickness: 38 μm) and heated at 130 ° C. for 3 minutes (the decomposition amount of peroxide obtained by calculation is About 88%) A pressure-sensitive adhesive layer having a thickness of 25 μm after drying was formed. The gel fraction of the pressure-sensitive adhesive layer immediately after drying was 60% by weight. Next, the pressure-sensitive adhesive layer was bonded to a polarizing plate and transferred to prepare a polarizing plate with a pressure-sensitive adhesive layer. In addition, the gel fraction after aging of an adhesive layer was 63 weight%.

Example 4
(Preparation of adhesive composition)
0.1 part of 3-aminopropyltriethoxysilane (manufactured by Shin-Etsu Silicone Co., KBE903), dibenzoyl peroxide (manufactured by Wako Pure Chemical Industries) 0 as a silane coupling agent with respect to 100 parts of the solid content of the acrylic polymer A solution .25 parts, trimethylolpropane hexamethylene diisocyanate adduct (D-160N) 0.05 part was added, and the mixture was uniformly mixed and stirred to prepare adhesive composition 4.

(Preparation of polarizing plate with adhesive layer)
The pressure-sensitive adhesive composition 4 was applied to one side of a silicone-treated PET film (Toray Industries, Inc., thickness: 38 μm) and heated at 130 ° C. for 3 minutes (the decomposition amount of peroxide obtained by calculation is About 88%) A pressure-sensitive adhesive layer having a thickness of 25 μm after drying was formed. The gel fraction of the pressure-sensitive adhesive layer immediately after drying was 60% by weight. Next, the pressure-sensitive adhesive layer was bonded to a polarizing plate and transferred to prepare a polarizing plate with a pressure-sensitive adhesive layer. In addition, the gel fraction after aging of an adhesive layer was 63 weight%.

Example 5
(Preparation of acrylic polymer B)
In a four-necked flask equipped with a stirring blade, a thermometer, a nitrogen gas inlet tube, and a condenser, 50 parts of hydrogenated terpene acrylate (manufactured by Yashara Chemical Co., TMA-2), 50 parts of butyl acrylate, 4-hydroxybutyl acrylate 5 parts, 0.5 part of acrylic acid, and 0.1 part of 2,2′-azobisisobutyronitrile (manufactured by Wako Pure Chemical Industries, Ltd.) as a polymerization initiator were charged together with 200 parts of ethyl acetate and sufficiently purged with nitrogen While stirring under a nitrogen stream, the temperature of the liquid in the flask was kept at around 60 ° C., and a polymerization reaction was carried out for 10 hours to prepare an acrylic polymer B solution. The resulting acrylic polymer B had a weight average molecular weight of 1.35 million.

(Preparation of adhesive composition)
For 100 parts of the solid content of the acrylic polymer B solution, 0.1 part of N-phenyl-3-aminopropyltrimethoxysilane (KBM573) as a silane coupling agent, hexamethylene diisocyanate adduct of trimethylolpropane (D- 160N) 0.25 parts was added, and the mixture was uniformly mixed and stirred to prepare an adhesive composition 5.

(Preparation of polarizing plate with adhesive layer)
The pressure-sensitive adhesive composition 5 was applied on one side of a silicone-treated PET film (Toray Industries, Inc., thickness: 38 μm), heated at 130 ° C. for 3 minutes, and dried to a thickness of 25 μm. Formed. The gel fraction of the pressure-sensitive adhesive layer immediately after drying was 65% by weight. Next, the pressure-sensitive adhesive layer was bonded to a polarizing plate and transferred to prepare a polarizing plate with a pressure-sensitive adhesive layer. In addition, the gel fraction after aging of an adhesive layer was 80 weight%.

Example 6
(Preparation of adhesive composition)
0.1 part of N-phenyl-3-aminopropyltrimethoxysilane (KBM573) as a silane coupling agent, dibenzoyl peroxide (manufactured by Wako Pure Chemical Industries) 0. 100 parts of solid content of the acrylic polymer B solution. 25 parts and 0.05 part of hexamethylene diisocyanate adduct (D-160N) of trimethylolpropane were added and mixed uniformly and stirred to prepare an adhesive composition 6.

(Preparation of polarizing plate with adhesive layer)
The pressure-sensitive adhesive composition 6 was applied on one side of a silicone-treated PET film (Toray Industries, Inc., thickness: 38 μm) and heated at 130 ° C. for 3 minutes (the decomposition amount of peroxide obtained by calculation is About 88%) A pressure-sensitive adhesive layer having a thickness of 25 μm after drying was formed. The gel fraction of the pressure-sensitive adhesive layer immediately after drying was 40% by weight. Next, the pressure-sensitive adhesive layer was bonded to a polarizing plate and transferred to prepare a polarizing plate with a pressure-sensitive adhesive layer. In addition, the gel fraction after aging of an adhesive layer was 55 weight%.

Example 7
(Preparation of acrylic polymer C)
In a four-necked flask equipped with a stirring blade, a thermometer, a nitrogen gas inlet tube, and a condenser, 100 parts of butyl acrylate, 0.5 part of 4-hydroxybutyl acrylate, 0.5 part of acrylic acid, 2, as a polymerization initiator After charging 0.1 part of 2′-azobisisobutyronitrile (manufactured by Wako Pure Chemical Industries, Ltd.) with 200 parts of ethyl acetate and sufficiently purging with nitrogen, the liquid temperature in the flask was adjusted to 60 ° C. while stirring under a nitrogen stream. A polymerization reaction was carried out for 10 hours while maintaining the vicinity to prepare an acrylic polymer C solution. The resulting acrylic polymer C had a weight average molecular weight of 1,680,000.

(Preparation of adhesive composition)
With respect to 100 parts of the solid content of the acrylic polymer C solution, 0.05 part of N-phenyl-3-aminopropyltrimethoxysilane (KBM573) as a silane coupling agent, hexamethylene diisocyanate adduct of trimethylolpropane (D- 160N) 0.15 part was added, and the mixture was uniformly mixed and stirred to prepare an adhesive composition 7.

(Preparation of polarizing plate with adhesive layer)
The pressure-sensitive adhesive composition 7 was applied to one side of a silicone-treated PET film (manufactured by Toray Industries, Inc., thickness: 38 μm), heated at 130 ° C. for 3 minutes, and dried to a thickness of 25 μm. Formed. The gel fraction of the pressure-sensitive adhesive layer immediately after drying was 53% by weight. Next, the pressure-sensitive adhesive layer was bonded to a polarizing plate and transferred to prepare a polarizing plate with a pressure-sensitive adhesive layer. In addition, the gel fraction after aging of an adhesive layer was 82 weight%.

Example 8
(Preparation of adhesive composition)
For 100 parts of the solid content of the acrylic polymer C solution, 0.1 part of 3-aminopropyltrimethoxysilane (manufactured by Shin-Etsu Silicone Co., Ltd., KBM903) as a silane coupling agent, dibenzoyl peroxide (manufactured by Wako Pure Chemical Industries) 0 .3 parts, 0.06 part of trimethylolpropane hexamethylene diisocyanate adduct (D-160N) was added, and the mixture was uniformly mixed and stirred to prepare PSA composition 8.

(Preparation of polarizing plate with adhesive layer)
The pressure-sensitive adhesive composition 8 was applied to one side of a silicone-treated PET film (manufactured by Toray Industries, Inc., thickness: 38 μm) and heated at 130 ° C. for 3 minutes. About 88%) A pressure-sensitive adhesive layer having a thickness of 25 μm after drying was formed. The gel fraction of the pressure-sensitive adhesive layer immediately after drying was 63% by weight. Next, the pressure-sensitive adhesive layer was bonded to a polarizing plate and transferred to prepare a polarizing plate with a pressure-sensitive adhesive layer. In addition, the gel fraction after aging of an adhesive layer was 77 weight%.

Example 9
(Preparation of adhesive composition)
As a silane coupling agent, 0.05 part of N-phenyl-3-aminopropyltrimethoxysilane (KBM573), dibenzoyl peroxide (manufactured by Wako Pure Chemical Industries) 3 parts, 0.02 part of trimethylolpropane hexamethylene diisocyanate adduct (D-160N) was added, and the mixture was uniformly mixed and stirred to prepare adhesive composition 9.

(Preparation of polarizing plate with adhesive layer)
The pressure-sensitive adhesive composition 9 was applied to one side of a silicone-treated PET film (manufactured by Toray Industries, Inc., thickness: 38 μm) and heated at 130 ° C. for 3 minutes (the decomposition amount of peroxide obtained by calculation is About 88%) A pressure-sensitive adhesive layer having a thickness of 25 μm after drying was formed. The gel fraction of the pressure-sensitive adhesive layer immediately after drying was 65% by weight. Next, the pressure-sensitive adhesive layer was bonded to a polarizing plate and transferred to prepare a polarizing plate with a pressure-sensitive adhesive layer. In addition, the gel fraction after aging of an adhesive layer was 77 weight%.

Example 10
(Preparation of adhesive composition)
To 100 parts of the solid content of the acrylic polymer C solution, 0.05 part of N-phenyl-3-aminopropyltrimethoxysilane (KBM573) as a silane coupling agent, and a tolylene diisocyanate adduct of trimethylolpropane (Nippon Polyurethane) Co., Ltd., Coronate L) 0.35 part was added, and the mixture was uniformly mixed and stirred to prepare an adhesive composition 10.

(Preparation of polarizing plate with adhesive layer)
The pressure-sensitive adhesive composition 10 was applied to one side of a silicone-treated PET film (manufactured by Toray Industries, Inc., thickness: 38 μm), heated at 130 ° C. for 3 minutes to form a pressure-sensitive adhesive layer having a thickness of 25 μm after drying. Formed. The gel fraction of the pressure-sensitive adhesive layer immediately after drying was 10% by weight. Next, the pressure-sensitive adhesive layer was bonded to a polarizing plate and transferred to prepare a polarizing plate with a pressure-sensitive adhesive layer. In addition, the gel fraction after aging of an adhesive layer was 88 weight%.

Comparative Example 1
(Preparation of adhesive composition)
For 100 parts of the solid content of the acrylic polymer A solution, 0.05 part of 3-glycidoxypropyltrimethoxysilane (manufactured by Shin-Etsu Silicone, KBM403) as a silane coupling agent, dibenzoyl peroxide (manufactured by Wako Pure Chemical Industries, Ltd.) ) 0.3 part, 0.02 part of hexamethylene diisocyanate adduct (D-160N) of trimethylolpropane was added, and the mixture was uniformly mixed and stirred to prepare adhesive composition 11.

(Preparation of polarizing plate with adhesive layer)
The adhesive composition 11 was applied to one side of a silicone-treated PET film (Toray Industries, Inc., thickness: 38 μm) and heated at 130 ° C. for 3 minutes (the amount of decomposition of the peroxide obtained by calculation is About 88%) A pressure-sensitive adhesive layer having a thickness of 25 μm after drying was formed. The gel fraction of the pressure-sensitive adhesive layer immediately after drying was 60% by weight. Next, the pressure-sensitive adhesive layer was bonded to a polarizing plate and transferred to prepare a polarizing plate with a pressure-sensitive adhesive layer. In addition, the gel fraction after aging of an adhesive layer was 68 weight%.

Comparative Example 2
(Preparation of adhesive composition)
As a silane coupling agent, 4.0 parts of N-phenyl-3-aminopropyltrimethoxysilane (KBM573), dibenzoyl peroxide (manufactured by Wako Pure Chemical Industries) 2 parts, 0.05 part of hexamethylene diisocyanate adduct (D-160N) of trimethylolpropane was added, and the mixture was uniformly mixed and stirred to prepare an adhesive composition 12.

(Preparation of polarizing plate with adhesive layer)
The pressure-sensitive adhesive composition 12 was applied to one side of a silicone-treated PET film (manufactured by Toray Industries, Inc., thickness: 38 μm) and heated at 130 ° C. for 3 minutes (the decomposition amount of peroxide obtained by calculation is About 88%) A pressure-sensitive adhesive layer having a thickness of 25 μm after drying was formed. The gel fraction of the pressure-sensitive adhesive layer immediately after drying was 1% by weight. Next, the pressure-sensitive adhesive layer was bonded to a polarizing plate and transferred to prepare a polarizing plate with a pressure-sensitive adhesive layer. In addition, the gel fraction after aging of an adhesive layer was 40 weight%.

Comparative Example 3
(Preparation of adhesive composition)
As a silane coupling agent, 0.3 part of 3-glycidoxypropyltrimethoxysilane (KBM403), 0.3 part of dibenzoyl peroxide (manufactured by Wako Pure Chemical Industries) as a silane coupling agent with respect to 100 parts of the solid content of the acrylic polymer C solution Then, 0.06 part of hexamethylene diisocyanate adduct (D-160N) of trimethylolpropane was added, and the mixture was uniformly mixed and stirred to prepare PSA composition 13.

(Preparation of polarizing plate with adhesive layer)
The pressure-sensitive adhesive composition 13 was applied to one side of a silicone-treated PET film (manufactured by Toray Industries, Inc., thickness: 38 μm) and heated at 130 ° C. for 3 minutes. About 88%) A pressure-sensitive adhesive layer having a thickness of 25 μm after drying was formed. The gel fraction of the pressure-sensitive adhesive layer immediately after drying was 66% by weight. Next, the pressure-sensitive adhesive layer was bonded to a polarizing plate and transferred to prepare a polarizing plate with a pressure-sensitive adhesive layer. In addition, the gel fraction after aging of an adhesive layer was 76 weight%.

Comparative Example 4
(Preparation of acrylic polymer D)
In a four-necked flask equipped with a stirring blade, a thermometer, a nitrogen gas inlet tube, and a condenser, 100 parts of butyl acrylate and 2,2′-azobisisobutyronitrile (manufactured by Wako Pure Chemical Industries, Ltd.) 0 as a polymerization initiator .1 part was charged together with 200 parts of ethyl acetate and sufficiently purged with nitrogen, and then the polymerization temperature was kept at around 60 ° C. while stirring under a nitrogen stream, and the polymerization reaction was carried out for 10 hours. Prepared. The resulting acrylic polymer D had a weight average molecular weight of 1,580,000.

(Preparation of adhesive composition)
As a silane coupling agent, 0.05 part of N-phenyl-3-aminopropyltrimethoxysilane (KBM573), dibenzoyl peroxide (manufactured by Wako Pure Chemical Industries) 3 parts were added, and it stirred uniformly and prepared the adhesive composition 14.

(Preparation of polarizing plate with adhesive layer)
The pressure-sensitive adhesive composition 14 was applied to one side of a silicone-treated PET film (Toray Industries, Inc., thickness: 38 μm) and heated at 130 ° C. for 3 minutes (the decomposition amount of peroxide obtained by calculation is About 88%) A pressure-sensitive adhesive layer having a thickness of 25 μm after drying was formed. The gel fraction of the pressure-sensitive adhesive layer immediately after drying was 54% by weight. Next, the pressure-sensitive adhesive layer was bonded to a polarizing plate and transferred to prepare a polarizing plate with a pressure-sensitive adhesive layer. In addition, the gel fraction after aging of an adhesive layer was 54 weight%.

Comparative Example 5
(Preparation of acrylic polymer E)
In a four-necked flask equipped with a stirring blade, thermometer, nitrogen gas inlet tube, and condenser, 50 parts of butyl acrylate, 50 parts of 2-ethylhexyl acrylate, 0.5 part of 2-hydroxyethyl acrylate, 0.5 part of acrylic acid Then, 0.1 part of 2,2′-azobisisobutyronitrile (manufactured by Wako Pure Chemical Industries, Ltd.) as a polymerization initiator was charged together with 200 parts of ethyl acetate, sufficiently purged with nitrogen, and then stirred while stirring under a nitrogen stream. The polymerization temperature was kept at around 60 ° C. for 9 hours to prepare an acrylic polymer E solution. The resulting acrylic polymer E had a weight average molecular weight of 1,650,000.

(Preparation of adhesive composition)
With respect to 100 parts of the solid content of the acrylic polymer E solution, 0.05 part of N-phenyl-3-aminopropyltrimethoxysilane (KBM573) as a silane coupling agent, hexamethylene diisocyanate adduct of trimethylolpropane (D- 160N) 0.15 part was added, and the mixture was stirred and mixed uniformly to prepare an adhesive composition 15.

(Preparation of polarizing plate with adhesive layer)
The pressure-sensitive adhesive composition 15 was applied on one side of a silicone-treated PET film (Toray Industries, Inc., thickness: 38 μm) and heated at 130 ° C. for 3 minutes to form a pressure-sensitive adhesive layer having a thickness of 25 μm after drying. Formed. The gel fraction of the pressure-sensitive adhesive layer immediately after drying was 2% by weight. Next, the pressure-sensitive adhesive layer was bonded to a polarizing plate and transferred to prepare a polarizing plate with a pressure-sensitive adhesive layer. In addition, the gel fraction after aging of an adhesive layer was 57 weight%.

  The following evaluation was performed about the polarizing plate (sample) with an adhesive layer obtained by the said Example and comparative example. The evaluation results are shown in Table 1.

<Measurement of initial adhesive strength>
The sample was cut to a width of 25 mm, attached to non-alkali glass (Corning Corp., 1737) by reciprocating with a 2 kg roller, treated in an autoclave at 50 ° C. and 0.5 MPa for 30 minutes, then 23 It was left to stand for 3 hours under the condition of ° C / 50% RH. The adhesive force (N / 25 cm) when the sample was peeled off with a tensile tester at a peeling angle of 90 ° and a peeling speed of 300 mm / min was measured.

<Measurement of adhesive strength and reworkability after 60 ° C./300 hours>
The sample was cut to a width of 25 mm, attached to non-alkali glass (Corning Corp., 1737) by reciprocating with a 2 kg roller, and treated in an autoclave at 50 ° C. and 0.5 Mpa for 30 minutes, then 60 ° C. For 300 hours, and then for 3 hours at 23 ° C. and 50% humidity. The adhesive force (N / 25 cm) when the sample was peeled off with a tensile tester at a peeling angle of 90 ° and a peeling speed of 300 mm / min was measured. Further, whether or not the pressure-sensitive adhesive layer or the optical member remains on the glass was visually observed and evaluated according to the following criteria.
○: No adhesive residue.
X: There is adhesive residue.

<Durability>
The sample was cut into 320 mm × 240 mm, attached to 0.7 mm-thick alkali-free glass (Corning Corp., # 1737), treated in an autoclave at 50 ° C. and 0.5 MPa for 15 minutes, and then subjected to 60 ° C. / It was left for 500 hours under the conditions of 90% RH (humidification test) or 80 ° C. (heat resistance test). Then, the state of the sample was visually evaluated according to the following criteria.
○: There is no peeling or floating of the polarizing plate.
X: There is peeling or floating of the polarizing plate.

<Processability>
The sample was punched using a press machine without aging treatment. At that time, the case where the pressure-sensitive adhesive layer was not attached to the cutting blade was evaluated as ◯, and the case where the pressure-sensitive adhesive layer was attached was evaluated as x.

  As described above, the pressure-sensitive adhesive optical member of the present invention is excellent in workability improvement by shortening the aging time and durability under long-term severe conditions. On the other hand, the pressure-sensitive adhesive optical member of the comparative example has an increased adhesive force when trying to improve the durability, and deteriorates when trying to reduce the adhesive force, making it difficult to achieve both. In addition, the adhesive optical member of the present invention has no adhesive residue even in a 60 ° C. long-term storage adhesion test, and has a low adhesive force even after being applied for a long period of time such as disposal, and it is easy to separate the glass from the optical member. I know that there is.

Claims (9)

1) As a monomer unit, 50% by weight or more of an alkyl (meth) acrylate having an alkyl group having 4 or more carbon atoms and 0.01 to 2% by weight of a monomer having an alkyl group having 4 to 12 carbon atoms and a hydroxyl group are contained. A (meth) acrylic polymer having a weight average molecular weight of 500,000 or more,
2) As a silane coupling agent, a silane compound having an amino group is 0.01 to 3 parts by weight with respect to 100 parts by weight of the (meth) acrylic polymer, and 3) the isocyanate-based crosslinking agent is the (meth) acrylic. A pressure-sensitive adhesive composition for optical members containing 0.01 to 2 parts by weight with respect to 100 parts by weight of a polymer.   Furthermore, the adhesive composition for optical members of Claim 1 which contains 0.02-2 weight part of organic peroxides with respect to 100 weight part of said (meth) acrylic-type polymers.   The pressure-sensitive adhesive composition for an optical member according to claim 1 or 2, wherein the amino group of the silane compound is a secondary amino group.   The pressure-sensitive adhesive composition for an optical member according to any one of claims 1 to 3, wherein the isocyanate-based crosslinking agent is an aliphatic isocyanate.   The pressure-sensitive adhesive composition for an optical member according to any one of claims 1 to 4, wherein the (meth) acrylic polymer further contains 0.01 to 2% by weight of a carboxyl group-containing monomer as a monomer unit.   The adhesive layer for optical members formed by carrying out the crosslinking reaction of the adhesive composition for optical members in any one of Claims 1-5.   The pressure-sensitive adhesive layer for an optical member according to claim 6, wherein the gel fraction is 45 to 90% by weight.   A pressure-sensitive adhesive optical member having the pressure-sensitive adhesive layer for an optical member according to claim 6 or 7 on one surface or both surfaces of the optical member.   An image display device using at least one adhesive optical member according to claim 8.