JP4859038B2 - Polarizing plate and image display device - Google Patents

Description

  The present invention relates to a polarizing plate and an image display device such as a liquid crystal display device, an organic EL display device, and a PDP that includes at least one polarizing plate.

  In the liquid crystal display device, it is indispensable to dispose polarizing plates on both sides of the glass substrate on which the liquid crystal panel surface is formed because of the image forming method. In general, a polarizing plate is obtained by attaching a polarizer protective film using triacetyl cellulose or the like to both surfaces of a polarizer made of a dichroic material such as a polyvinyl alcohol film and iodine with a polyvinyl alcohol adhesive. Things are used.

  In recent years, liquid crystal display devices have been used more frequently at high temperatures or in high humidity outdoors such as mobile terminals and car navigation systems. Therefore, development of a polarizing plate excellent in heat resistance and moisture resistance is desired.

  Triacetylcellulose has insufficient heat resistance and moisture resistance, and if a polarizing plate using a triacetylcellulose film as a polarizer protective film is used at high temperature or high humidity, the performance of the polarizing plate, such as the degree of polarization and hue, will decrease. There is a drawback of doing. In addition, the triacetyl cellulose film produces a phase difference with respect to incident light in an oblique direction. Such a phase difference significantly affects viewing angle characteristics as the size of liquid crystal displays increases in recent years.

  Therefore, a transparent thermoplastic resin has been studied as a material for a polarizer protective film that replaces conventional triacetyl cellulose. In particular, (meth) acrylic resins such as acrylic acid esters and methacrylic acid esters have been studied because they are excellent in optical transparency and relatively excellent in heat resistance and moisture resistance.

  However, when the conventional polarizing plate is placed in an environment of high temperature or high humidity, there is a problem that the adhesiveness between the polarizer and the polarizer protective film is greatly reduced, and it becomes easy to peel off each other or the optical properties are deteriorated. is there.

As one of the measures for improving the adhesion between a polarizer and a polarizer protective film in an environment of high temperature or high humidity, a technique using a polyvinyl alcohol-based adhesive containing glyoxal and zinc chloride has been reported (patent) Reference 1). However, the adhesion between the polarizer and the polarizer protective film in an environment of high temperature or high humidity is still not sufficient. Moreover, since the polyvinyl alcohol-type adhesive conventionally used widely cannot be used as it is, manufacturing efficiency will fall.
JP 7-134212 A

  The present invention has been made in order to solve the above-described conventional problems. The object of the present invention is (1) extremely excellent adhesion between a polarizer and a polarizer protective film in an environment of high temperature or high humidity. Providing a polarizing plate that has excellent optical characteristics and can be applied with a conventional general-purpose adhesive layer and has few appearance defects, and (2) provides a high-quality image display device using such a polarizing plate. To do.

  The polarizing plate according to the present invention includes a polarizer, an adhesive layer, a metal salt layer, and a polarizer protective film formed in this order from a polyvinyl alcohol resin.

  In a preferred embodiment, the adhesive layer is a layer formed from a polyvinyl alcohol-based adhesive.

  In a preferred embodiment, the metal salt layer is a layer formed from at least one selected from a zinc salt and a cobalt salt.

  In preferable embodiment, the said polarizer protective film contains a (meth) acrylic-type resin layer.

  In preferable embodiment, it has further an adhesive layer as at least one of outermost layers.

  According to another aspect of the present invention, an image display device is provided. The image display device of the present invention includes at least one polarizing plate of the present invention.

According to the present invention, the adhesion between the polarizer and the polarizer protective film in an environment of high temperature or high humidity is extremely excellent, the optical properties are excellent, and a conventional general-purpose adhesive layer can be applied. Can be provided. In addition, a high-quality image display device using such a polarizing plate can be provided.
The polarizing plate and the image display device of the present invention are excellent in optical properties, heat resistance, and moisture resistance, so that they can be used not only in normal use but also in outdoor or high temperature or high humidity environments such as mobile terminals and car navigation systems. It is also suitable for use in

  Hereinafter, although preferable embodiment of this invention is described, this invention is not limited to these embodiment.

[Polarizer protective film]
The polarizer protective film in this invention is not specifically limited, What is necessary is just a film containing a resin layer with high optical transparency. For example, a film including a layer formed from a cellulose-based resin (cellulose-based resin layer) and a film including a layer formed from a (meth) acrylic-based resin ((meth) acrylic-based resin layer) can be given. The polarizer protective film in the present invention may be a single layer film or a film composed of two or more layers. The polarizer protective film in the present invention preferably includes a (meth) acrylic resin layer.

  Although it does not specifically limit as said cellulose resin, A triacetyl cellulose is preferable at the point of transparency and adhesiveness.

Although it does not specifically limit as said (meth) acrylic-type resin, For example, poly (meth) acrylic acid ester, such as polymethyl methacrylate, methyl methacrylate- (meth) acrylic acid copolymer, methyl methacrylate- (meta ) Acrylic acid ester copolymer, methyl methacrylate-acrylic acid ester- (meth) acrylic acid copolymer, (meth) methyl acrylate-styrene copolymer (MS resin, etc.), alicyclic hydrocarbon group Polymers (for example, methyl methacrylate-cyclohexyl methacrylate copolymer, methyl methacrylate-norbornyl (meth) acrylate copolymer, etc.) and the like can be mentioned. Preferably, poly (meth) acrylate C _1-6 alkyl such as poly (meth) acrylate methyl, particularly preferably methyl methacrylate as the main component (50-100 wt%, preferably 70-100 wt%). And methyl methacrylate resin.

  The (meth) acrylic resin preferably has a Tg (glass transition temperature) of 120 ° C. or higher, more preferably 125 ° C. or higher, and still more preferably 130 ° C. or higher. By including a (meth) acrylic resin having a Tg (glass transition temperature) of 120 ° C. or higher as a main component, for example, when it is finally incorporated into a polarizing plate, it tends to be excellent in durability. The upper limit of Tg of the (meth) acrylic resin is not particularly limited, but is preferably 300 ° C. or less, more preferably 290 ° C. or less, and further preferably 285 ° C. or less from the viewpoint of moldability and the like.

  Specific examples of the (meth) acrylic resin 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. Examples of the resin include high Tg (meth) acrylic resins obtained by intramolecular crosslinking or intramolecular cyclization reaction. Moreover, the (meth) acrylic-type resin which has a lactone ring structure as described in Unexamined-Japanese-Patent No. 2002-120326 and Unexamined-Japanese-Patent No. 2002-254544 is mentioned.

  The (meth) acrylic resin preferably has high light transmittance, low in-plane retardation Δnd and low thickness direction retardation Rth.

  The thickness of the polarizer protective film in this invention becomes like this. Preferably it is 20-200 micrometers, More preferably, it is 25-180 micrometers, More preferably, it is 30-140 micrometers. When the thickness of the polarizer protective film is 20 μm or more, it has appropriate strength and rigidity, and handling properties are good during secondary processing such as laminating and printing. Further, the phase difference caused by the stress at the time of take-up can be easily controlled, and the film can be manufactured stably and easily. When the thickness of the polarizer protective film is 200 μm or less, film winding becomes easy, and line speed, productivity, and controllability become easy.

  When the polarizer protective film in this invention contains (meth) acrylic-type resin, content of (meth) acrylic-type resin in a polarizer protective film becomes like this. Preferably it is 50 to 99 weight%, More preferably, it is 60 to 98 weight%. %, More preferably 70 to 97% by weight. When the content of the (meth) acrylic resin in the polarizer protective film is less than 50% by weight, the high heat resistance and high transparency inherent in the (meth) acrylic resin may not be sufficiently reflected, If it exceeds 99% by weight, the mechanical strength may be inferior.

  In the polarizer protective film of the present invention, an ultraviolet absorber, a general compounding agent such as a stabilizer, a lubricant, a processing aid, a plasticizer, an impact aid, a retardation reducing agent, a matting agent, an antibacterial agent. Agents, fungicides, etc. may be included.

YI in the thickness of 80 μm of the polarizer protective film in the present invention is preferably 1.3 or less, more preferably 1.27 or less, further preferably 1.25 or less, further preferably 1.23 or less, and particularly preferably 1. 20 or less. If YI at a thickness of 80 μm exceeds 1.3, excellent optical transparency may not be exhibited. YI is obtained from tristimulus values (X, Y, Z) of colors obtained by measurement using, for example, a high-speed integrating sphere type spectral transmittance measuring machine (trade name DOT-3C: manufactured by Murakami Color Research Laboratory). The following equation can be used.
YI = [(1.28X−1.06Z) / Y] × 100

  The b value (a measure of hue according to Hunter's color system) at a thickness of 80 μm of the polarizer protective film in the present invention is preferably less than 1.5, more preferably 1.0 or less. When b value is 1.5 or more, there is a possibility that excellent optical transparency may not be exhibited due to coloring of the film. In addition, b value measures a hue using a high-speed integrating-sphere type spectral transmittance measuring machine (trade name DOT-3C: manufactured by Murakami Color Research Laboratory), for example, by cutting a polarizer protective film sample into a 3 cm square. be able to. Moreover, a hue can be evaluated by b value according to Hunter's color system.

  In the polarizer protective film of the present invention, the in-plane retardation Δnd is preferably 3.0 nm or less, more preferably 1.0 nm or less. If the in-plane retardation Δnd exceeds 3.0 nm, the effects of the present invention, in particular, excellent optical characteristics may not be exhibited. The thickness direction retardation Rth is preferably 5.0 nm or less, more preferably 3.0 nm or less. When the thickness direction retardation Rth exceeds 5.0 nm, the effects of the present invention, in particular, excellent optical characteristics may not be exhibited.

In the polarizer protective film in the present invention, the moisture permeability is preferably 100 g / m ² · 24 hr or less, more preferably 60 g / m ² · 24 hr or less. If the moisture permeability exceeds 100 g / m ² · 24 hr, the moisture resistance may be inferior.

The polarizer protective film in the present invention preferably also has excellent mechanical strength. Tensile strength, in the MD direction, preferably 65N / mm ² or more, more preferably 70N / mm ² or more, more preferably 75N / mm ² or more, particularly preferably 80 N / mm ² or more, in the TD direction, preferably the 45N / mm ² or more, more preferably 50 N / mm ² or more, more preferably 55N / mm ² or more, and particularly preferably 60N / mm ² or more. The tensile elongation is preferably 6.5% or more, more preferably 7.0% or more, further preferably 7.5% or more, particularly preferably 8.0% or more in the MD direction, and preferably in the TD direction. Is 5.0% or more, more preferably 5.5% or more, still more preferably 6.0% or more, and particularly preferably 6.5% or more. When the tensile strength or tensile elongation is out of the above range, there is a possibility that excellent mechanical strength may not be exhibited.

  The polarizer protective film of the present invention has a lower haze that represents optical transparency, and is preferably 5% or less, more preferably 3% or less, still more preferably 1.5% or less, and particularly preferably 1%. % Or less. When the haze is 5% or less, it is possible to visually give a good clear feeling to the film. When the haze is 1.5% or less, even when used as a lighting member such as a window, the visibility and the lighting performance are improved. Since both can be obtained, and even when used as a front plate of a display device, the display contents can be visually recognized well, and thus the industrial utility value is high.

  The polarizer protective film in the present invention may be produced by any method, but the resin composition forming the film is extruded (melt extrusion method such as T-die method or inflation method), cast molding ( A melt casting method, etc.) and a method of producing by calendering are preferred.

  Extrusion molding does not require drying and scattering of the solvent in the adhesive used during processing, such as the organic solvent in the adhesive for dry lamination, as in the case of the dry lamination method. Excellent in productivity. Specifically, there can be exemplified a method of forming a film by supplying a resin composition as a raw material to an extruder connected to a T-die, and after melt-kneading, extruding, cooling with water and taking it out. The screw type of the extruder may be uniaxial or biaxial, and an additive such as a plasticizer or an antioxidant may be added.

  The extrusion molding temperature can be appropriately set, but when the glass transition temperature of the resin composition as a raw material is Tg (° C.), (Tg + 80) ° C. to (Tg + 180) ° C. is preferable, and (Tg + 100) ° C. to (Tg + 150) ° C. More preferred. If the extrusion molding temperature is too low, the resin does not have fluidity and may not be molded. If the extrusion molding temperature is too high, the resin viscosity will be low, and there may be a problem in production stability such as uneven thickness of the molded product.

  In the resin composition forming the polarizer protective film in the present invention, an ultraviolet absorber, a general compounding agent, for example, a stabilizer, a lubricant, a processing aid, a plasticizer, an impact resistance aid, a phase difference reducing agent. Matting agents, antibacterial agents, fungicides, etc. may be included.

  As an optical characteristic of the polarizer protective film, the magnitude of the retardation in the front and thickness directions becomes a problem. Therefore, it is preferable that the resin composition which forms the polarizer protective film in this invention contains the phase difference reducing agent. As the retardation reducing agent, for example, styrene-containing polymers such as acrylonitrile-styrene block copolymer and acrylonitrile-styrene block copolymer copolymer are preferable. The addition amount of the retardation reducing agent is preferably 30% by weight or less, more preferably 25% by weight or less, and further preferably 20% by weight or less with respect to the (meth) acrylic resin. When added exceeding this range, visible light is scattered or transparency is impaired, so that the properties as a polarizer protective film may be lacking.

  The polarizer protective film in this invention can be laminated | stacked and used for another base material. For example, it can be laminated by multilayer extrusion molding including an adhesive resin layer or multilayer inflation molding on a substrate such as glass, a polyolefin resin, an ethylene vinylidene copolymer serving as a high barrier layer, or polyester. If the heat-fusibility is high, the adhesive layer may be omitted.

  The polarizer protective film in the present invention is not only used for protecting the polarizer, but also, for example, a building lighting member such as a window or a carport roof material, a vehicle lighting member such as a window, an agricultural lighting member such as a greenhouse, and an illumination. It can be used by being laminated on a member, a display member such as a front filter, etc., and a housing of home appliances, vehicle interior members, interior building materials, wallpaper, It can also be used by laminating on decorative panels, entrance doors, window frames, baseboards, and the like.

〔Polarizer〕
The polarizing plate of the present invention has a polarizer, an adhesive layer, a metal salt layer, and a polarizer protective film formed in this order from a polyvinyl alcohol-based resin. In one preferred embodiment of the polarizing plate of the present invention, as shown in FIG. 1, one surface of a polarizer 31 is protected by a polarizer through an adhesive layer 32, an easy adhesion layer 33, and a metal salt layer 34. It is bonded to the film 35, and the other surface of the polarizer 31 is bonded to the polarizer protective film 37 through the adhesive layer 36. An easy-adhesion layer may exist between the adhesive layer 36 and the polarizer protective film 37.

  As the polarizer formed from the polyvinyl alcohol-based resin, one obtained by dyeing a polyvinyl alcohol-based resin film with a dichroic substance (typically iodine, a dichroic dye) and uniaxially stretching is used. The polymerization degree of the polyvinyl alcohol resin constituting the polyvinyl alcohol resin film is preferably 100 to 5000, and more preferably 1400 to 4000. The polyvinyl alcohol-based resin film constituting the polarizer can be formed by any suitable method (for example, a casting method in which a solution obtained by dissolving a resin in water or an organic solvent is cast, a casting method, an extrusion method). . The thickness of the polarizer can be appropriately set according to the purpose and application of the LCD in which the polarizing plate is used, but is typically 5 to 80 μm.

  As a method for producing a polarizer, any appropriate method can be adopted depending on the purpose, materials used, conditions, and the like. Typically, a method is employed in which the polyvinyl alcohol-based resin film is subjected to a series of production steps including swelling, dyeing, crosslinking, stretching, washing with water, and drying steps. In each processing step except the drying step, the treatment is performed by immersing the polyvinyl alcohol-based resin film in a bath containing a solution used in each step. The order, frequency, and presence / absence of each treatment of swelling, dyeing, crosslinking, stretching, washing with water, and drying can be appropriately set according to the purpose, materials used, conditions, and the like. For example, several processes may be performed simultaneously in one process, and a specific process may be omitted. More specifically, for example, the stretching process may be performed after the dyeing process, may be performed before the dyeing process, or may be performed simultaneously with the swelling process, the dyeing process, and the crosslinking process. Further, for example, it can be suitably employed to perform the crosslinking treatment before and after the stretching treatment. Further, for example, the water washing process may be performed after all the processes, or may be performed only after a specific process.

  The swelling step is typically performed by immersing the polyvinyl alcohol resin film in a treatment bath (swelling bath) filled with water. By this treatment, dirt on the surface of the polyvinyl alcohol-based resin film and an anti-blocking agent can be washed, and unevenness such as uneven dyeing can be prevented by swelling the polyvinyl alcohol-based resin film. Glycerin, potassium iodide, or the like can be appropriately added to the swelling bath. The temperature of the swelling bath is typically about 20 to 60 ° C., and the immersion time in the swelling bath is typically about 0.1 to 10 minutes.

  The dyeing step is typically performed by immersing the polyvinyl alcohol-based resin film in a treatment bath (dye bath) containing a dichroic substance such as iodine. As the solvent used for the dye bath solution, water is generally used, but an appropriate amount of an organic solvent compatible with water may be added. The dichroic substance is typically used at a ratio of 0.1 to 1.0 part by weight with respect to 100 parts by weight of the solvent. When iodine is used as the dichroic substance, the dye bath solution preferably further contains an auxiliary agent such as iodide. This is because the dyeing efficiency is improved. The auxiliary is preferably used in a proportion of 0.02 to 20 parts by weight, more preferably 2 to 10 parts by weight, with respect to 100 parts by weight of the solvent. Specific examples of iodide include potassium iodide, lithium iodide, sodium iodide, zinc iodide, aluminum iodide, lead iodide, copper iodide, barium iodide, calcium iodide, tin iodide, and iodide. Titanium is mentioned. The temperature of the dyeing bath is typically about 20 to 70 ° C., and the immersion time in the dyeing bath is typically about 1 to 20 minutes.

  The crosslinking step is typically performed by immersing the dyed polyvinyl alcohol resin film in a treatment bath (crosslinking bath) containing a crosslinking agent. Arbitrary appropriate crosslinking agents can be employ | adopted as a crosslinking agent. Specific examples of the crosslinking agent include boron compounds such as boric acid and borax, glyoxal, and glutaraldehyde. These can be used alone or in combination. As the solvent used for the solution of the crosslinking bath, water is generally used, but an appropriate amount of an organic solvent having compatibility with water may be added. The crosslinking agent is typically used at a ratio of 1 to 10 parts by weight with respect to 100 parts by weight of the solvent. When the concentration of the crosslinking agent is less than 1 part by weight, sufficient optical properties cannot often be obtained. When the concentration of the crosslinking agent exceeds 10 parts by weight, the stretching force generated in the film during stretching increases, and the resulting polarizing plate may shrink. The solution of the crosslinking bath preferably further contains an auxiliary agent such as iodide. This is because it is easy to obtain uniform characteristics in the plane. The concentration of the auxiliary agent is preferably 0.05 to 15% by weight, more preferably 0.5 to 8% by weight. Specific examples of iodide are the same as those in the dyeing process. The temperature of the crosslinking bath is typically about 20 to 70 ° C, preferably 40 to 60 ° C. The immersion time in the crosslinking bath is typically about 1 second to 15 minutes, preferably 5 seconds to 10 minutes.

  The stretching process may be performed at any stage as described above. Specifically, it may be performed after the dyeing process, may be performed before the dyeing process, may be performed simultaneously with the swelling process, the dyeing process, and the crosslinking process, or may be performed after the crosslinking process. The cumulative draw ratio of the polyvinyl alcohol-based resin film needs to be 5 times or more, preferably 5 to 7 times, and more preferably 5 to 6.5 times. When the cumulative draw ratio is less than 5 times, it may be difficult to obtain a polarizing plate with a high degree of polarization. When the cumulative draw ratio exceeds 7 times, the polyvinyl alcohol-based resin film (polarizer) may be easily broken. Arbitrary appropriate methods may be employ | adopted as a specific method of extending | stretching. For example, when the wet stretching method is adopted, the polyvinyl alcohol-based resin film is stretched at a predetermined magnification in a treatment bath (stretching bath). As the stretching bath solution, a solution in which various metal salts, iodine, boron or zinc compounds are added to a solvent such as water or an organic solvent (for example, ethanol) is preferably used.

  The water washing step is typically performed by immersing the polyvinyl alcohol-based resin film subjected to the above-described various treatments in a treatment bath (water washing bath). An unnecessary residue of the polyvinyl alcohol-based resin film can be washed away by the water washing step. The washing bath may be pure water or an aqueous solution of iodide (for example, potassium iodide or sodium iodide). The concentration of the iodide aqueous solution is preferably 0.1 to 10% by mass. An auxiliary agent such as zinc sulfate or zinc chloride may be added to the aqueous iodide solution. The temperature of the washing bath is preferably 10 to 60 ° C, more preferably 30 to 40 ° C. The immersion time is typically 1 second to 1 minute. The water washing step may be performed only once, or may be performed a plurality of times as necessary. When implemented several times, the kind and density | concentration of the additive contained in the washing bath used for each process can be adjusted suitably. For example, the water washing step includes a step of immersing the polymer film in an aqueous potassium iodide solution (0.1 to 10% by mass, 10 to 60 ° C.) for 1 second to 1 minute, and a step of rinsing with pure water.

  Any appropriate drying method (for example, natural drying, air drying, heat drying) may be employed as the drying step. For example, in the case of heat drying, the drying temperature is typically 20 to 80 ° C., and the drying time is typically 1 to 10 minutes. A polarizer is obtained as described above.

  In the polarizing plate of this invention, it has an adhesive bond layer between the said polarizer protective film and the said polarizer.

  In the present invention, the adhesive layer is preferably a layer formed from a polyvinyl alcohol-based adhesive. The polyvinyl alcohol-based adhesive contains a polyvinyl alcohol-based resin and a crosslinking agent.

  The polyvinyl alcohol-based resin is not particularly limited. For example, polyvinyl alcohol obtained by saponifying polyvinyl acetate; a derivative thereof; and a saponified product of a copolymer with a monomer having copolymerizability with vinyl acetate. Modified polyvinyl alcohol obtained by acetalization, urethanization, etherification, grafting, phosphoric esterification, etc. of polyvinyl alcohol. Examples of the monomer include unsaturated carboxylic acids such as (anhydrous) maleic acid, fumaric acid, crotonic acid, itaconic acid, (meth) acrylic acid, and esters thereof; α-olefins such as ethylene and propylene, (meth) Examples include allyl sulfonic acid (soda), sulfonic acid soda (monoalkyl malate), disulfonic acid soda alkyl maleate, N-methylol acrylamide, acrylamide alkyl sulfonic acid alkali salt, N-vinyl pyrrolidone, N-vinyl pyrrolidone derivatives, and the like. . These polyvinyl alcohol resins may be used alone or in combination of two or more.

  From the viewpoint of adhesiveness, the polyvinyl alcohol-based resin preferably has an average degree of polymerization of 100 to 3000, more preferably 500 to 3000, and an average degree of saponification of preferably 85 to 100 mol%, more preferably 90. ˜100 mol%.

  As the polyvinyl alcohol resin, a polyvinyl alcohol resin having an acetoacetyl group can be used. A polyvinyl alcohol-based resin having an acetoacetyl group is a polyvinyl alcohol-based adhesive having a highly reactive functional group, and is preferable in terms of improving the durability of the polarizing plate.

  A polyvinyl alcohol-based resin containing an acetoacetyl group is obtained by reacting a polyvinyl alcohol-based resin with diketene by a known method. For example, a method in which a polyvinyl alcohol resin is dispersed in a solvent such as acetic acid and diketene is added thereto, and a polyvinyl alcohol resin is previously dissolved in a solvent such as dimethylformamide or dioxane, and diketene is added thereto. And the like. Moreover, the method of making diketene gas or liquid diketene contact directly to polyvinyl alcohol is mentioned.

  The degree of acetoacetyl group modification of the polyvinyl alcohol resin having an acetoacetyl group is not particularly limited as long as it is 0.1 mol% or more. If it is less than 0.1 mol%, the water resistance of the adhesive layer is insufficient, which is inappropriate. The degree of acetoacetyl modification is preferably 0.1 to 40 mol%, more preferably 1 to 20 mol%. When the degree of acetoacetyl modification exceeds 40 mol%, the number of reaction points with the cross-linking agent decreases, and the effect of improving water resistance is small. The degree of acetoacetyl modification is a value measured by NMR.

As said crosslinking agent, what is used for the polyvinyl alcohol-type adhesive agent can be especially used without a restriction | limiting.
As the crosslinking agent, a compound having at least two functional groups having reactivity with the polyvinyl alcohol resin can be used. For example, alkylene diamines having two alkylene groups and two amino groups such as ethylene diamine, triethylene amine, hexamethylene diamine (hexamethylene diamine is preferred); tolylene diisocyanate, hydrogenated tolylene diisocyanate, trimethylene propane tolylene Isocyanate adduct, triphenylmethane triisocyanate, methylene bis (4-phenylmethane triisocyanate, isophorone diisocyanate and isocyanates such as ketoxime block or phenol block; ethylene glycol diglycidyl ether, polyethylene glycol diglycidyl ether, glycerin di Or triglycidyl ether, 1,6-hexanediol diglycidyl ether, trimethylo Epoxys such as rupropane triglycidyl ether, diglycidyl aniline, diglycidyl amine; monoaldehydes such as formaldehyde, acetaldehyde, propionaldehyde, butyraldehyde; glyoxal, malondialdehyde, succindialdehyde, glutardialdehyde, maleidialdehyde , Dialdehydes such as phthaldialdehyde; amino-formaldehyde resins such as methylol urea, methylol melamine, alkylated methylol urea, alkylated methylolated melamine, acetoguanamine, condensates of benzoguanamine and formaldehyde; sodium, potassium, magnesium Divalent metals such as calcium, aluminum, iron and nickel, or salts of trivalent metals and oxides thereof. Is to, melamine-based crosslinking agent is preferably, suitable in particular melamine.

  The amount of the crosslinking agent is preferably 0.1 to 35 parts by weight, more preferably 10 to 25 parts by weight with respect to 100 parts by weight of the polyvinyl alcohol resin. On the other hand, in order to further improve the durability, the crosslinking agent can be blended in a range of more than 30 parts by weight and 46 parts by weight or less with respect to 100 parts by weight of the polyvinyl alcohol resin. In particular, when a polyvinyl alcohol-based resin containing an acetoacetyl group is used, it is preferable to use the crosslinking agent in an amount exceeding 30 parts by weight. Water resistance improves by mix | blending a crosslinking agent in the range of more than 30 weight part and 46 weight part or less.

  The polyvinyl alcohol-based adhesive further includes coupling agents such as silane coupling agents and titanium coupling agents, various tackifiers, ultraviolet absorbers, antioxidants, heat stabilizers, hydrolysis stabilizers, and the like. A stabilizer or the like can also be blended.

  The metal salt layer of the polarizing plate of the present invention is not particularly limited as long as it is a layer formed from at least one metal salt, and examples thereof include iron salts, cobalt salts, nickel salts, copper salts, and zinc salts. However, it is preferably a layer formed of at least one selected from zinc salts and cobalt salts.

  Examples of the zinc salt include zinc chloride and zinc sulfate.

  Examples of the cobalt salt include cobalt chloride and cobalt sulfate.

  The thickness of the metal salt layer is preferably 5 to 150 nm, more preferably 10 to 100 nm, and still more preferably 30 to 70 nm.

  The metal salt layer can be formed by any appropriate method. One preferred embodiment is a method in which an aqueous solution containing at least one metal salt is applied onto a polarizer protective film and dried.

  When forming the metal salt layer on the polarizer protective film, the surface of the polarizer protective film on which the metal salt layer is formed is subjected to easy adhesion treatment such as corona treatment, plasma treatment, low-pressure UV treatment, and saponification treatment. In particular, it is more preferable to perform a corona treatment.

  The polarizing plate of the present invention has a metal salt layer between the polarizer protective film and the adhesive layer. For this reason, it is thought that the reaction between the functional group of the polarizer protective film and the metal and the reaction between the adhesive layer and the metal occur, and the excellent adhesion between the polarizer and the polarizer protective film is exhibited. it can.

  The polarizer protective film in this invention can form an easily bonding layer for the adhesive improvement in the surface side which contact | connects a polarizer. When a metal salt layer is provided on the polarizer protective film, an easy adhesion layer may be formed on the metal salt layer.

  As said easily bonding layer, the silicone layer which has a reactive functional group is mentioned, for example. The material of the silicone layer having a reactive functional group is not particularly limited. For example, an isocyanate group-containing alkoxysilanol, an amino group-containing alkoxysilanol, a mercapto group-containing alkoxysilanol, a carboxy-containing alkoxysilanol, an epoxy group-containing Examples thereof include alkoxysilanols, vinyl-type unsaturated group-containing alkoxysilanols, halogen group-containing alkoxylanols, and isocyanate group-containing alkoxysilanols, and amino silanols are preferred. Furthermore, the adhesive force can be strengthened by adding a titanium-based catalyst or a tin-based catalyst for efficiently reacting the silanol. Moreover, you may add another additive to the silicone which has the said reactive functional group. Specifically, terpene resins, phenol resins, terpene-phenol resins, rosin resins, xylene resins and other tackifiers, UV absorbers, antioxidants, heat stabilizers and other stabilizers may be used.

  The silicone layer having the reactive functional group is formed by coating and drying by a known technique. The thickness of the silicone layer is preferably 1 to 100 nm, more preferably 10 to 50 nm after drying. During coating, silicone having a reactive functional group may be diluted with a solvent. The dilution solvent is not particularly limited, and examples thereof include alcohols. The dilution concentration is not particularly limited, but is preferably 1 to 5% by weight, more preferably 1 to 3% by weight.

  The adhesive layer is formed by applying the adhesive to either side or both sides of the polarizer protective film and to either side or both sides of the polarizer. After bonding a polarizer protective film and a polarizer, a drying process is given and the adhesive bond layer which consists of an application | coating drying layer is formed. This can also be bonded after forming the adhesive layer. Bonding of a polarizer and a polarizer protective film can be performed with a roll laminator or the like. The heating and drying temperature and drying time are appropriately determined according to the type of adhesive.

  The thickness of the adhesive layer is preferably 0.01 to 10 μm, and more preferably 0.03 to 5 μm, because it is not preferable in terms of adhesiveness of the polarizer protective film if the thickness after drying becomes too thick. .

  Bonding of the polarizer protective film to the polarizer can be bonded to both sides of the polarizer on one side of the polarizer protective film.

  In addition, the polarizer protective film of the polarizer can be bonded to one side of the polarizer by bonding on one side of the polarizer protective film, and the cellulose resin can be bonded to the other side.

  The cellulose resin is not particularly limited, but triacetyl cellulose is preferable in terms of transparency and adhesiveness. The thickness of the cellulosic resin is preferably 30 to 100 μm, more preferably 40 to 80 μm. If the thickness is less than 30 μm, the film strength is lowered and workability is inferior.

  The polarizing plate of the present invention may have an adhesive layer as at least one of the outermost layers (such a polarizing plate may be referred to as an adhesive polarizing plate). As a particularly preferred embodiment, a pressure-sensitive adhesive layer for adhering to another member such as another optical film or a liquid crystal cell can be provided on the side of the polarizer protective film where the polarizer is not adhered.

  The pressure-sensitive adhesive forming the pressure-sensitive adhesive layer is not particularly limited. For example, an acrylic polymer, silicone polymer, polyester, polyurethane, polyamide, polyether, fluorine-based or rubber-based polymer is used as a base polymer. It can select suitably and can be used. In particular, those having excellent optical transparency such as an acrylic pressure-sensitive adhesive, exhibiting appropriate wettability, cohesiveness, and adhesive pressure-sensitive adhesive properties, and being excellent in weather resistance and heat resistance can be preferably used. In particular, an acrylic pressure-sensitive adhesive made of an acrylic polymer having 4 to 12 carbon atoms is preferable.

  In addition to the above, in terms of prevention of foaming and peeling phenomena due to moisture absorption, deterioration of optical properties and liquid crystal cell warpage due to differences in thermal expansion, etc., as well as formability of liquid crystal display devices with high quality and excellent durability An adhesive layer having a low moisture absorption rate and excellent heat resistance is preferred.

  The pressure-sensitive adhesive layer is, for example, a natural or synthetic resin, in particular, a tackifier resin, a filler or pigment made of glass fiber, glass beads, metal powder, other inorganic powders, a colorant, an antioxidant. An additive to be added to the pressure-sensitive adhesive layer such as an agent may be contained.

  Moreover, the adhesive layer etc. which contain microparticles | fine-particles and show light diffusibility may be sufficient.

  The attachment of the pressure-sensitive adhesive layer can be performed by an appropriate method. For example, a pressure sensitive adhesive solution of about 10 to 40% by weight in which a base polymer or a composition thereof is dissolved or dispersed in a solvent composed of a suitable solvent alone or a mixture such as toluene and ethyl acetate is prepared. A method in which it is directly attached on a polarizing plate or an optical film by an appropriate development method such as a casting method or a coating method, or a pressure-sensitive adhesive layer is formed on a separator according to the above, and the surface is applied to a polarizer protective film. The method of transferring to is included.

  The pressure-sensitive adhesive layer can be provided on one side or both sides of the polarizing plate as a superposed layer of different compositions or types. Moreover, when providing in both surfaces, it can also be set as adhesive layers with a different composition, a kind, thickness, etc. in the front and back of a polarizing plate.

  The thickness of the pressure-sensitive adhesive layer can be appropriately determined according to the purpose of use and adhesive force, and is preferably 1 to 40 μm, more preferably 5 to 30 μm, and particularly preferably 10 to 25 μm. When the thickness is less than 1 μm, the durability is deteriorated. When the thickness is more than 40 μm, floating or peeling due to foaming or the like is liable to occur, resulting in poor appearance.

  In order to improve the adhesion between the polarizer protective film and the pressure-sensitive adhesive layer, an anchor layer may be provided between the layers.

  As the anchor layer, an anchor layer selected from polyurethane, polyester and polymers containing an amino group in the molecule is preferably used, and polymers containing an amino group in the molecule are particularly preferably used. Polymers containing amino groups in the molecule are good because the amino groups in the molecule exhibit interactions such as reaction or ionic interaction with carboxyl groups in the adhesive and polar groups in the conductive polymer. Adhesion is ensured.

  Examples of the polymer containing an amino group in the molecule include, for example, polyethyleneimine, polyallylamine, polyvinylamine, polyvinylpyridine, polyvinylpyrrolidine, and amino-containing groups such as dimethylaminoethyl acrylate shown as a copolymer monomer of the acrylic pressure-sensitive adhesive. Examples thereof include polymers of contained monomers.

  In order to impart antistatic properties to the anchor layer, an antistatic agent may be added. Antistatic agents for imparting antistatic properties include ionic surfactant systems, conductive polymer systems such as polyaniline, polythiophene, polypyrrole, and polyquinoxaline, and metal oxide systems such as tin oxide, antimony oxide, and indium oxide. In particular, a conductive polymer system is preferably used from the viewpoint of optical characteristics, appearance, antistatic effect, and stability of the antistatic effect when heated and humidified. Among these, water-soluble conductive polymers such as polyaniline and polythiophene or water-dispersible conductive polymers are particularly preferably used. This is because, when a water-soluble conductive polymer or a water-dispersible conductive polymer is used as a material for forming the antistatic layer, it is possible to suppress deterioration of the optical film substrate due to an organic solvent during the coating process.

  In the present invention, the polarizer, polarizer protective film, and the like that form the polarizing plate described above, and the pressure-sensitive adhesive layer, for example, salicylic acid ester compounds, benzophenol compounds, benzotriazole compounds, and cyanoacrylate compounds. A compound or a compound having ultraviolet absorbing ability by a method such as a method of treating with a UV absorber such as a nickel complex salt compound may be used.

  The polarizing plate of the present invention may be provided on either the viewing side or the backlight side of the liquid crystal cell or on both sides, and is not limited.

  Next, the image display apparatus of the present invention will be described. The image display device of the present invention includes at least one polarizing plate of the present invention. Here, a liquid crystal display device will be described as an example, but it goes without saying that the present invention can be applied to any display device that requires a polarizing plate. Specific examples of the image display device to which the polarizing plate of the present invention can be applied include a self-luminous display device such as an electroluminescence (EL) display, a plasma display (PD), and a field emission display (FED: Field Emission Display). Can be mentioned. FIG. 2 is a schematic cross-sectional view of a liquid crystal display device according to a preferred embodiment of the present invention. In the illustrated example, a transmissive liquid crystal display device will be described, but it goes without saying that the present invention is also applied to a reflective liquid crystal display device and the like.

  The liquid crystal display device 100 includes a liquid crystal cell 10, retardation films 20 and 20 ′ disposed across the liquid crystal cell 10, and polarizing plates 30 and 30 ′ disposed outside the retardation films 20 and 20 ′. A light guide plate 40, a light source 50, and a reflector 60 are provided. The polarizing plates 30 and 30 'are arranged so that their polarization axes are orthogonal to each other. The liquid crystal cell 10 includes a pair of glass substrates 11 and 11 ′ and a liquid crystal layer 12 as a display medium disposed between the substrates. One substrate 11 is provided with a switching element (typically a TFT) for controlling the electro-optical characteristics of the liquid crystal, a scanning line for supplying a gate signal to the switching element, and a signal line for supplying a source signal ( Neither is shown). The other glass substrate 11 ′ is provided with a color layer constituting a color filter and a light shielding layer (black matrix layer) (both not shown). The distance (cell gap) between the substrates 11 and 11 ′ is controlled by the spacer 13. In the liquid crystal display device of the present invention, the polarizing plate of the present invention described above is employed as at least one of the polarizing plates 30 and 30 '.

  For example, in the case of the TN mode, in such a liquid crystal display device 100, when no voltage is applied, the liquid crystal molecules of the liquid crystal layer 12 are arranged in a state where the polarization axis is shifted by 90 degrees. In such a state, incident light that is transmitted through only light in one direction by the polarizing plate is twisted 90 degrees by liquid crystal molecules. As described above, since the polarizing plates are arranged so that the polarization axes thereof are orthogonal to each other, the light (polarized light) reaching the other polarizing plate is transmitted through the polarizing plate. Therefore, when no voltage is applied, the liquid crystal display device 100 performs white display (normally white method). On the other hand, when a voltage is applied to such a liquid crystal display device 100, the arrangement of liquid crystal molecules in the liquid crystal layer 12 changes. As a result, the light (polarized light) that has reached the other polarizing plate cannot be transmitted through the polarizing plate, resulting in black display. An image is formed by switching such display for each pixel using an active element.

  EXAMPLES Hereinafter, although an Example demonstrates this invention concretely, this invention is not limited to these Examples. Unless otherwise indicated, parts and percentages in the examples are based on weight.

<Heat shock test>
A sample obtained by cutting a polarizing plate into a 15-inch size was repeatedly subjected to holding at −40 ° C. for 30 minutes and holding at 85 ° C. for 30 minutes alternately, and the amount of change in light transmittance (%) and sample after 240 hours The amount of color loss (mm) at the end was measured. In addition, the light transmittance of the sample was measured using a high-speed integrating sphere type spectral transmittance measuring device (trade name DOT-3C: manufactured by Murakami Color Research Laboratory).

<Warm water immersion test>
A sample obtained by cutting the polarizing plate into 25 mm × 50 mm (the long side and the polarizer absorption axis are parallel) was immersed in hot water at 60 ° C., and the amount of peeling (mm) at the end of the sample was measured after 10 hours.

<Single transmittance, degree of polarization>
Sample pieces having a size of 5 cm in length and 5 cm in width were cut out from the polarizing plates produced in Examples and Comparative Examples, and a high-speed integrating sphere type spectral transmittance measuring machine (trade name DOT-3C: manufactured by Murakami Color Research Laboratory) was used. The single transmittance and polarization degree were measured at 23 ° C.

<Rework test>
An adhesive polarizing plate was prepared as described below, and a rework test was performed.
(Formation of adhesive layer)
As a base polymer, a solution (solid content 30) containing an acrylic polymer having a weight average molecular weight of 2 million consisting of a copolymer of butyl acrylate: acrylic acid: 2-hydroxyethyl acrylate = 100: 5: 0.1 (weight ratio) %) Was used. 4 parts of Coronate L manufactured by Nippon Polyurethane Co., Ltd., which is an isocyanate-based polyfunctional compound, is added to the acrylic polymer solution, and 0.5 parts of additives (trade name: KBM403, manufactured by Shin-Etsu Silicone Co., Ltd.) Part, a solvent for adjusting viscosity (ethyl acetate) was added to prepare an adhesive solution (solid content 12%). After applying the adhesive solution on a release film (polyethylene terephthalate base material, product name: Diafoil MRF38, manufactured by Mitsubishi Chemical Polyester Co., Ltd.) so that the thickness after drying is 25 μm, in a hot air circulation oven It dried and the adhesive layer was formed.
(Polarizing plate anchor layer)
A polyethyleneimine adduct of polyacrylic acid ester (manufactured by Nippon Shokubai Co., Ltd., trade name: Poliment NK380) was diluted 50 times with methyl isobutyl ketone. This was coated and dried on the surface of the polarizing plate prepared in Examples and Comparative Examples on the polymethyl methacrylate layer side using a wire bar # 5 so that the thickness after drying was 50 nm, thereby forming an anchor layer.
(Preparation of adhesive polarizing plate)
The release film on which the pressure-sensitive adhesive layer was formed was bonded to the anchor layer provided on the polarizing plate to produce a pressure-sensitive adhesive polarizing plate.
(Rework)
A sample piece having a size of 150 mm × 90 mm is cut out from the pressure-sensitive adhesive polarizing plate so that the absorption axis of the polarizing plate is 0 ° parallel to the long side direction, the release film is peeled off, and the pressure-sensitive adhesive layer is made alkali-free. After being attached to glass, it was treated in an autoclave at 50 ° C. and 5 × 10 ⁵ Pa ( ⁵ atm) for 15 minutes. The polarizing plate attached to the glass plate thus obtained was peeled off from the glass plate in parallel with the long side direction from the short side of the polarizing plate. About this polarizing plate produced by the Example and the comparative example, this operation was implemented 3 times each, and the presence or absence of peeling in the interface of the polarizer of a polarizing plate and a protective film (laminated film or a triacetyl cellulose film) was observed. The results of the rework test shown in Table 2 are shown as the number of samples (the number of samples without peeling / 3) of the samples that did not peel during the above three operations.

<Preparation of polyvinyl alcohol adhesive aqueous solution>
A polyvinyl alcohol adhesive aqueous solution prepared by adjusting an aqueous solution containing 20 parts by weight of methylolmelamine to 100 parts by weight of an acetoacetyl-modified polyvinyl alcohol resin (degree of acetylation 13%) to a concentration of 0.5% by weight Prepared.

[Example 1]
(A) Production of laminated film (1A) A 40 μm-thick polymethyl methacrylate film was subjected to corona discharge treatment (irradiation amount: 50 w / m ² / min). Subsequently, a zinc chloride aqueous solution (10% by weight) was applied to the surface subjected to the corona discharge treatment, and dried at 85 ° C. for 5 minutes. Further, a silicon primer solution (3% by weight) was applied as an undercoating treatment and dried at 70 ° C. for 10 minutes.
The thickness of each layer of the obtained laminated film (1A) after drying was polymethyl methacrylate layer / zinc chloride layer / silicon primer layer = 40 μm / 50 nm / 50 nm.
(B) Production of Polarizer Film A polyvinyl alcohol film (manufactured by Kuraray, trade name: VS75RS) was swollen with hot water at 30 ° C., and subsequently dyed in an aqueous iodine solution at 30 ° C. Further, crosslinking was carried out with a 40 ° C. boric acid aqueous solution (3 wt%), and uniaxial stretching was carried out with a 60 ° C. boric acid aqueous solution (5 wt%). Thereafter, the film hue was adjusted and the film surface was washed in a 30 ° C. water washing step. After washing with water and drying at 40 ° C. for 5 minutes, a polarizer film (1B) was produced.
(C) Production of Polarizing Plate (1C) A triacetyl cellulose film is formed on one side of the polarizer film (1B) produced in (b) above, and a laminated film (1A) produced in (a) on the other side. The silicon primer layer surface of) was bonded with a polyvinyl alcohol adhesive and dried at 80 ° C. for 10 minutes to produce a polarizing plate (1C).
Table 1 shows the results of conducting a heat shock test and a hot water immersion test on the polarizing plate (1C). Table 2 shows the results of single transmittance measurement, polarization degree measurement, and rework test on the polarizing plate (1C).

[Example 2]
(A) Production of laminated film (2A) A 40 μm-thick polymethyl methacrylate film was subjected to corona discharge treatment (irradiation amount: 50 w / m ² / min). Subsequently, a zinc chloride aqueous solution (10% by weight) was applied to the surface subjected to the corona discharge treatment, and dried at 85 ° C. for 5 minutes. Further, a silicon primer solution (3% by weight) was applied as an undercoating treatment and dried at 70 ° C. for 10 minutes.
The thickness of each layer of the obtained laminated film (2A) after drying was polymethyl methacrylate layer / zinc chloride layer / silicone primer layer = 40 μm / 50 nm / 100 nm.
(B) Production of Polarizer Film A polyvinyl alcohol film (manufactured by Kuraray, trade name: VS75RS) was swollen with hot water at 30 ° C., and subsequently dyed in an aqueous iodine solution at 30 ° C. Further, crosslinking was carried out with a 40 ° C. boric acid aqueous solution (3 wt%), and uniaxial stretching was carried out with a 60 ° C. boric acid aqueous solution (5 wt%). Thereafter, the film hue was adjusted and the film surface was washed in a 30 ° C. water washing step. After washing with water and drying at 40 ° C. for 5 minutes, a polarizer film (2B) was produced.
(C) Preparation of Polarizing Plate (2C) Triacetylcellulose film is formed on one surface of polarizer film (2B) prepared in (b) above, and laminated film (2A) prepared on (a) on the other surface. The silicon primer layer surface of) was bonded with a polyvinyl alcohol adhesive and dried at 80 ° C. for 10 minutes to produce a polarizing plate (2C).
Table 1 shows the results of conducting a heat shock test and a hot water immersion test on the polarizing plate (2C). Table 2 shows the results of the single transmittance measurement, the polarization degree measurement, and the rework test for the polarizing plate (2C).

Example 3
(A) Preparation of laminated film (3A) A polymethylmethacrylate film having a thickness of 40 μm was subjected to corona discharge treatment (irradiation amount: 50 w / m ² / min). Subsequently, a cobalt chloride aqueous solution (10% by weight) was applied to the surface subjected to the corona discharge treatment and dried at 85 ° C. for 5 minutes. Further, a silicon primer solution (3% by weight) was applied as an undercoating treatment and dried at 70 ° C. for 10 minutes.
The thickness of each layer of the obtained laminated film (3A) after drying was polymethyl methacrylate layer / cobalt chloride layer / silicon primer layer = 40 μm / 50 nm / 50 nm.
(B) Production of Polarizer Film A polyvinyl alcohol film (manufactured by Kuraray, trade name: VS75RS) was swollen with hot water at 30 ° C., and subsequently dyed in an aqueous iodine solution at 30 ° C. Further, crosslinking was carried out with a 40 ° C. boric acid aqueous solution (3 wt%), and uniaxial stretching was carried out with a 60 ° C. boric acid aqueous solution (5 wt%). Thereafter, the film hue was adjusted and the film surface was washed in a 30 ° C. water washing step. After washing with water and drying at 40 ° C. for 5 minutes, a polarizer film (3B) was produced.
(C) Production of Polarizing Plate (3C) A triacetylcellulose film is formed on one surface of the polarizer film (3B) produced in (b) above, and a laminated film (3A) produced in (a) on the other surface. The silicon primer layer surface of) was bonded with a polyvinyl alcohol-based adhesive and dried at 80 ° C. for 10 minutes to produce a polarizing plate (3C).
Table 1 shows the results of the heat shock test and the hot water immersion test for the polarizing plate (3C). In addition, Table 2 shows the results of single transmittance measurement, polarization degree measurement, and rework test for the polarizing plate (3C).

[Comparative Example 1]
(A) Production of laminated film (C1A) A 40 μm-thick polymethyl methacrylate film was subjected to corona discharge treatment (irradiation amount: 50 w / m ² / min). Subsequently, a silicon primer solution (3% by weight) was applied as an undercoating treatment to the surface subjected to the corona discharge treatment, and dried at 70 ° C. for 10 minutes.
The thickness of each layer of the obtained laminated film (C1A) after drying was polymethyl methacrylate layer / silicone primer layer = 40 μm / 50 nm.
(B) Production of Polarizer Film A polyvinyl alcohol film (manufactured by Kuraray, trade name: VS75RS) was swollen with hot water at 30 ° C., and subsequently dyed in an aqueous iodine solution at 30 ° C. Further, crosslinking was carried out with a 40 ° C. boric acid aqueous solution (3 wt%), and uniaxial stretching was carried out with a 60 ° C. boric acid aqueous solution (5 wt%). Thereafter, the film hue was adjusted and the film surface was washed in a 30 ° C. water washing step. After washing with water and drying at 40 ° C. for 5 minutes, a polarizer film (C1B) was produced.
(C) Production of Polarizing Plate (C1C) One side of the polarizer film (C1B) produced in (b) above is a triacetyl cellulose film, and the other side is a laminated film (C1A) produced in (a). ) Was bonded with a polyvinyl alcohol-based adhesive and dried at 80 ° C. for 10 minutes to produce a polarizing plate (C1C).
Table 1 shows the results of the heat shock test and the hot water immersion test for the polarizing plate (C1C). Table 2 shows the results of the single transmittance measurement, the polarization degree measurement, and the rework test for the polarizing plate (C1C).

[Comparative Example 2]
(A) Production of film (C2A) A polymethylmethacrylate film having a thickness of 40 μm was subjected to corona discharge treatment (irradiation amount: 50 w / m ² / min) to produce a film (C2A).
(B) Production of Polarizer Film A polyvinyl alcohol film (manufactured by Kuraray, trade name: VS75RS) was swollen with hot water at 30 ° C., and subsequently dyed in an aqueous iodine solution at 30 ° C. Further, crosslinking was carried out with a 40 ° C. boric acid aqueous solution (3 wt%), and uniaxial stretching was carried out with a 60 ° C. boric acid aqueous solution (5 wt%). Thereafter, the film hue was adjusted and the film surface was washed in a 30 ° C. water washing step. After washing with water and drying at 40 ° C. for 5 minutes, a polarizer film (C2B) was produced.
(C) Preparation of polarizing plate (C2C) Triacetylcellulose film is formed on one surface of polarizer film (C2B) prepared in (b) above, and film (C2A) prepared on (a) on the other surface. The corona discharge-treated surfaces were bonded with a polyvinyl alcohol adhesive and dried at 80 ° C. for 10 minutes to produce a polarizing plate (C2C).
Table 1 shows the results of conducting a heat shock test and a hot water immersion test on the polarizing plate (C2C). Table 2 shows the results of the single transmittance measurement, the polarization degree measurement, and the rework test for the polarizing plate (C2C).

  In Examples 1 to 3, compared with Comparative Examples 1 and 2, both the light transmittance change amount and the color loss amount at the end portion in the heat shock test are small, and the amount of peeling in the warm water immersion test is also small. No peeling of the polarizer and the protective film was observed.

It is sectional drawing which shows an example of the polarizing plate of this invention. 1 is a schematic cross-sectional view of a liquid crystal display device according to a preferred embodiment of the present invention.

Explanation of symbols

DESCRIPTION OF SYMBOLS 10 Liquid crystal cell 11, 11 'Glass substrate 12 Liquid crystal layer 13 Spacer 20, 20' Retardation film 30, 30 'Polarizing plate 31 Polarizer 32 Adhesive layer 33 Easy adhesion layer 34 Metal salt layer 35 Polarizer protective film 36 Adhesive Layer 37 Polarizer protective film 40 Light guide plate 50 Light source 60 Reflector 100 Liquid crystal display device

Claims (7)

Polarizer formed of a polyvinyl alcohol-based resin, the adhesive layer, adhesive layer, metal salt layer, the polarizer protective film and perforated in this order, from at least one said metal salt layer is selected from zinc salts and cobalt salts A polarizing plate which is a layer to be formed .   The polarizing plate according to claim 1, wherein the easy adhesion layer is a silicone layer having a reactive functional group, and the thickness of the silicone layer is 1 to 100 nm.   The polarizing plate according to claim 1 or 2, wherein the metal salt layer has a thickness of 5 to 150 nm.   The polarizing plate according to claim 1, wherein the adhesive layer is a layer formed from a polyvinyl alcohol-based adhesive. The polarizer protective film, (meth) acrylic resin layer, a polarizing plate according to any one of claims 1 to 4. Further comprising a pressure-sensitive adhesive layer as at least one of an outermost layer, polarizing plate according to any one of claims 1 to 5. Comprising at least one polarizing plate according to any one of claims 1 to 6, the image display device.

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