Polarizing plate and image display device

Abstract

To provide a polarizing plate in which a decrease in transmittance in a high temperature environment is suppressed.SOLUTION: Disclosed a polarizing plate which includes: a polarizing element in which a dichroic dye is adsorbed and aligned on a polyvinyl alcohol resin layer; a first transparent protective film laminated on one surface of the polarizing element; and a second transparent protective film laminated on the other surface of the polarizing element. The polarizing element and the transparent protective film are bonded together by a first adhesive layer formed of a first adhesive containing a first compound. The polarizing element and the second transparent protective film are bonded together by a second adhesive layer formed of a second adhesive containing a second compound. The first compound is at least one kind selected from the group consisting of urea, urea derivative, thiourea and thiourea derivative, and the second compound has a nitroxy radical or a nitroxide group.SELECTED DRAWING: None

Description

[Technical field]

[0001] The present invention relates to a polarizing plate and an image display device. [Background technology]

[0002] Liquid crystal display devices (LCDs) are widely used not only in liquid crystal televisions, but also in personal computers, mobile devices such as mobile phones, and in-vehicle applications such as car navigation systems. Typically, liquid crystal display devices have a liquid crystal panel with polarizing plates attached to both sides of a liquid crystal cell with an adhesive, and display is performed by controlling light from a backlight with the liquid crystal panel. In recent years, organic electroluminescence (EL) display devices have also been widely used in televisions, mobile devices such as mobile phones, and in-vehicle applications such as car navigation systems, similar to liquid crystal display devices. In organic EL display devices, a circular polarizing plate (a laminate including a polarizing element and a λ / 4 plate) may be placed on the viewing side surface of the image display panel to prevent external light from being reflected by a metal electrode (cathode) and being viewed as a mirror surface.

[0003] As mentioned above, polarizing plates are increasingly being installed in vehicles as components of image display devices such as liquid crystal display devices, organic electroluminescence display devices, etc. Polarizing plates used in in-vehicle image display devices are more often exposed to high-temperature environments than those used in mobile applications such as televisions and mobile phones, and are therefore required to have small changes in properties at high temperatures (high-temperature durability).

[0004] On the other hand, for the purpose of preventing damage to the image display panel due to impact from the outer surface, a configuration in which a front panel such as a transparent resin plate or a glass plate (also called a "window layer") is provided on the viewing side of the image display panel is increasingly being adopted. In image display devices equipped with a touch panel, a configuration in which the touch panel is provided on the viewing side of the image display panel and a front panel is provided on the further viewing side of the touch panel is widely adopted.

[0005] In such a configuration, if there is an air layer between the image display panel and a transparent member such as a front plate or a touch panel, the external light is reflected at the interface of the air layer, and the visibility of the screen tends to decrease. Therefore, there is a growing trend to adopt a configuration (hereinafter, sometimes referred to as an "interlayer filling configuration") in which the space between the polarizing plate and the transparent member arranged on the viewing side surface of the image display panel is filled with a layer other than the air layer, which is usually a solid layer (hereinafter, sometimes referred to as an "interlayer filling agent"). The interlayer filling agent is preferably a material whose refractive index is close to that of the polarizing plate or the transparent member. As the interlayer filling agent, a pressure sensitive adhesive or a UV curable adhesive is used for the purpose of suppressing the decrease in visibility due to the reflection at the interface and bonding and fixing each member (see, for example, Patent Document 1).

[0006] The interlayer filling structure is being widely adopted for mobile applications such as mobile phones that are often used outdoors. In addition, due to the increasing demand for visibility in recent years, the adoption of an interlayer filling structure in which a front transparent plate is placed on the surface of an image display panel and an adhesive layer or the like is filled between the panel and the front transparent plate is being considered for in-vehicle applications such as car navigation devices.

[0007] However, it has been reported that when such a configuration is adopted, the transmittance of the polarizing plate significantly decreases in a high-temperature environment. As a solution to this problem, Patent Document 2 proposes a method of suppressing the decrease in transmittance by setting the moisture content per unit area of ​​the polarizing plate to a specified amount or less and setting the saturated water absorption amount of the transparent protective film adjacent to the polarizing element to a specified amount or less. [Prior art documents] [Patent documents]

[0008] [Patent Document 1] Japanese Patent Application Publication No. 11-174417 [Patent Document 2] JP 2014-102353 A Summary of the Invention [Problem to be solved by the invention]

[0009] However, even such a polarizing plate does not have a sufficient effect of suppressing a decrease in durability in a high-temperature environment. An object of the present invention is to provide a novel polarizing plate capable of suppressing a decrease in transmittance even when exposed to a high-temperature environment, and an image display device using the polarizing plate. [Means for solving the problem]

[0010] The present invention provides a polarizing plate and an image display device as exemplified below. [1] A polarizing plate comprising a polarizing element having a polyvinyl alcohol-based resin layer in which a dichroic dye is adsorbed and oriented, a first transparent protective film laminated on one surface of the polarizing element, and a second transparent protective film laminated on the other surface of the polarizing element, the polarizing element and the first transparent protective film are bonded to each other by a first adhesive layer formed from a first adhesive containing a first compound; the polarizing element and the second transparent protective film are attached to each other by a second adhesive layer formed from a second adhesive containing a second compound; the first compound is at least one selected from the group consisting of urea, urea derivatives, thiourea, and thiourea derivatives; A polarizing plate, wherein the second compound is a compound having a nitroxy radical or a nitroxide group. [2] The polarizing plate according to [1], wherein the second compound is an N-oxyl compound. [3] The polarizing plate according to [1] or [2], wherein the first compound is at least one urea compound selected from the group consisting of urea derivatives and thiourea derivatives. [4] The polarizing plate according to any one of [1] to [3], wherein the first adhesive and the second adhesive contain a polyvinyl alcohol-based resin. [5] The polarizing plate according to [4], wherein the content of the first compound in the first adhesive is 0.1 parts by mass or more and 400 parts by mass or less per 100 parts by mass of the polyvinyl alcohol-based resin. [6] The polarizing plate according to [4] or [5], wherein the content of the second compound in the second adhesive is 0.1 parts by mass or more and 400 parts by mass or less per 100 parts by mass of the polyvinyl alcohol-based resin. [7] The polarizing plate according to any one of [1] to [6], wherein the first adhesive layer and the second adhesive layer have a thickness of 0.01 μm or more and 7 μm or less. [8] The polarizing plate is used in an image display device, The polarizing plate according to any one of [1] to [7], wherein in the image display device, solid layers are provided on both sides of the polarizing plate in contact with each other. [9] An image display device comprising: an image display cell; a first pressure-sensitive adhesive layer laminated on a viewing-side surface of the image display cell; and the polarizing plate described in any one of [1] to [8] laminated on the viewing-side surface of the first pressure-sensitive adhesive layer.

[10] The image display device described in [9], further comprising a second adhesive layer laminated on the viewing side surface of the polarizing plate, and a transparent member laminated on the viewing side surface of the second adhesive layer.

[11] The image display device according to

[10] , wherein the transparent member is a glass plate or a transparent resin plate.

[12] The image display device according to

[10] , wherein the transparent member is a touch panel. Effect of the Invention

[0011] According to the present invention, it is possible to provide a polarizing plate having improved high-temperature durability and suppressing a decrease in transmittance even when exposed to a high-temperature environment, even when used in an image display device having an interlayer filling structure. Furthermore, by using the polarizing plate according to the present invention, it is possible to provide an image display device having suppressed a decrease in transmittance even when exposed to a high-temperature environment. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0012] Hereinafter, an embodiment of the present invention will be described, however, the present invention is not limited to the following embodiment.

[0013] [Polarizing plate] A polarizing plate according to an embodiment of the present invention includes a polarizing element having a dichroic dye adsorbed and aligned in a layer containing a polyvinyl alcohol-based resin, a first transparent protective film laminated on one surface of the polarizing element, and a second transparent protective film laminated on the other surface of the polarizing element. The polarizing element and the first transparent protective film are bonded together with a first adhesive layer formed from a first adhesive containing a first compound. The polarizing element and the second transparent protective film are bonded together with a second adhesive layer formed from a second adhesive containing a second compound.

[0014] The first compound is at least one selected from the group consisting of urea, urea derivatives, thiourea, and thiourea derivatives, and the second compound is a compound having a nitroxy radical or a nitroxide group.

[0015] As a conventional polarizing plate having excellent high-temperature durability, for example, a polarizing plate in which the decrease in transmittance is suppressed even when the polarizing plate is left alone in an environment at a temperature of 95°C for 1000 hours is known. However, even such a polarizing plate, when used in an interlayer filling structure, may show a significant decrease in transmittance in the center of the polarizing plate plane when left in an environment at a temperature of 95°C for 200 hours. In addition, when the moisture content of the polarizing plate or polarizing element is out of a specific range, a significant decrease in transmittance or polarization degree may be seen in the center of the polarizing plate plane. It is considered that a significant decrease in the transmittance of a polarizing plate in a high-temperature environment is a problem that is particularly likely to occur when an image display device employing an interlayer filling structure in which one surface of a polarizing plate is bonded to an image display cell and the other surface is bonded to a transparent member such as a touch panel or a front panel is exposed to a high-temperature environment.

[0016] The polarizing plate with a significantly reduced transmittance due to the interlayer filling structure was measured by Raman spectroscopy at 1100 cm -1 near (derived from the C-C bond) and 1500 cm -1 Since there is a peak near the -C=C bond, it is considered to be a polyene structure (-C=C). nThe polyene structure is presumably formed when the polyvinyl alcohol constituting the polarizing element is dehydrated to form a polyene structure (Patent Document 2, paragraph

[0012] ).

[0017] The polarizing plate according to the present invention can further improve the high temperature durability. The polarizing plate according to the present invention can be incorporated into an image display device having an interlayer filling configuration, and can suppress the decrease in transmittance even when exposed to a high temperature environment of, for example, a temperature of 105°C. It is speculated that such an effect is due to the synergistic action of the first compound and the second compound present in the adhesive layer, which suppresses the polyenation of polyvinyl alcohol constituting the polarizing element. It has been confirmed that such an effect is not limited to the case where the moisture content of the polarizing plate or polarizing element is within a specific range, but is exerted even when the moisture content of the polarizing plate or polarizing element is low or high. It is speculated that this is because when the moisture content of the polarizing plate or polarizing element is low, the effect of suppressing the polyenation of polyvinyl alcohol by the first compound becomes more significant, while when the moisture content of the polarizing plate or polarizing element is high, the effect of suppressing the polyenation of polyvinyl alcohol by the second compound becomes more significant.

[0018] The polarizing plate according to this embodiment can have at least one of the following characteristics (a) and (b). (a) The moisture content of the polarizing element is equal to or greater than the equilibrium moisture content at a temperature of 20° C. and a relative humidity of 30% and equal to or less than the equilibrium moisture content at a temperature of 20° C. and a relative humidity of 80%. (b) The moisture content of the polarizing plate is equal to or greater than the equilibrium moisture content at a temperature of 20° C. and a relative humidity of 30% and equal to or less than the equilibrium moisture content at a temperature of 20° C. and a relative humidity of 80%. The polarizing plate of this embodiment has the effect of improving high-temperature durability even when it has a more limited characteristic than the above characteristic (a) or (b), such as the following characteristic (a1) or (b1). (a1) The moisture content of the polarizing element is greater than the equilibrium moisture content at a temperature of 20° C. and a relative humidity of 45% or 50%, and is less than or equal to the equilibrium moisture content at a temperature of 20° C. and a relative humidity of 80% or 70%. (b1) The moisture content of the polarizing plate is greater than the equilibrium moisture content at a temperature of 20° C. and a relative humidity of 45% or 50%, and is less than or equal to the equilibrium moisture content at a temperature of 20° C. and a relative humidity of 80% or 70%. Even if the polarizing plate does not have a step of adjusting the moisture content, it is usually highly likely to have the above characteristics (a) and (b). In this embodiment, the polarizing plate may have a step of adjusting the moisture content so as to have at least one of the above characteristics (a) and (b), or may not have a step of adjusting the moisture content.

[0019] <Polarizing element> A well-known polarizing element can be used as the polarizing element in which a dichroic dye is adsorbed and aligned in a layer containing a polyvinyl alcohol (hereinafter also referred to as "PVA")-based resin (hereinafter also referred to as a "PVA-based resin layer"). Examples of the polarizing element include a stretched film obtained by dyeing a PVA-based resin film with a dichroic dye and uniaxially stretching it, and a stretched layer obtained by using a laminated film having a coating layer formed by applying a coating liquid containing a PVA-based resin onto a base film, dyeing the coating layer with a dichroic dye, and uniaxially stretching the laminated film. The stretching may be performed after dyeing with the dichroic dye, may be performed while dyeing, or may be performed after stretching and dyeing.

[0020] PVA resins are obtained by saponifying polyvinyl acetate resins. Examples of polyvinyl acetate resins include polyvinyl acetate, which is a homopolymer of vinyl acetate, and copolymers of vinyl acetate with other monomers that can be copolymerized with it. Examples of other copolymerizable monomers include unsaturated carboxylic acids, olefins such as ethylene, vinyl ethers, and unsaturated sulfonic acids.

[0021] The saponification degree of the PVA resin is preferably about 85 mol% or more, more preferably about 90 mol% or more, and even more preferably about 99 mol% or more and 100 mol% or less. The polymerization degree of the PVA resin is, for example, 1000 to 10000, preferably 1500 to 5000. The PVA resin may be modified, and may be, for example, polyvinyl formal, polyvinyl acetal, polyvinyl butyral, etc., modified with aldehydes.

[0022] The thickness of the polarizing element is preferably 3 μm or more and 35 μm or less, more preferably 4 μm or more and 30 μm or less, and even more preferably 5 μm or more and 25 μm or less. By making the thickness of the polarizing element 35 μm or less, the influence of the polyenation of the PVA resin on the deterioration of optical properties in a high temperature environment can be suppressed. By making the thickness of the polarizing element 3 μm or more, it becomes easy to make a configuration that achieves the desired optical properties.

[0023] The polarizing element preferably contains a first compound and a second compound. In this embodiment, the polarizing element and the first transparent protective film are bonded together by a first adhesive layer formed from a first adhesive containing the first compound, and the polarizing element and the second transparent protective film are bonded together by a second adhesive layer formed from a second adhesive containing the second compound. It is presumed that a part of the first compound transferred from the first adhesive layer and a part of the second compound transferred from the second adhesive layer are contained in the polarizing element. The first compound and the second compound in the polarizing element may contain compounds added during the manufacturing process of the polarizing element. By providing the first adhesive layer containing the first compound and the second adhesive layer containing the second compound, the transmittance is less likely to decrease even when the polarizing plate is exposed to a high-temperature environment. In addition, by providing the first adhesive layer containing the first compound and the second adhesive layer containing the second compound, the decrease in the degree of polarization can be suppressed even when the polarizing plate is exposed to a high-temperature environment. When two polarizing plates are arranged in a crossed Nicol relationship, if the polarization degree of the polarizing plates is reduced, light leakage (hereinafter also referred to as "cross leakage") is likely to occur, but according to the present invention, the polarization degree is unlikely to decrease even when exposed to a high temperature environment, so cross leakage is also easily suppressed. This is presumably because the polyenization of the PVA resin is suppressed by the synergistic effect of the first compound and the second compound contained in the polarizing element.

[0024] The method of incorporating the first compound and the second compound during the manufacture of a polarizing element includes a method of immersing a PVA-based resin layer in a treatment solvent containing the first compound and / or the second compound, or a method of spraying, flowing or dropping the treatment solvent onto the PVA-based resin layer. Among these, a method of immersing a PVA-based resin layer in a treatment solvent containing both the first compound and the second compound is preferably used. Specific examples of the first compound and the second compound include those exemplified as those to be incorporated into the adhesive described later.

[0025] The process of immersing the PVA-based resin layer in a treatment solvent containing the first and second compounds may be performed simultaneously with the processes of swelling, stretching, dyeing, crosslinking, washing, etc. in the manufacturing method of a polarizing element described later, or may be provided separately from these processes. The process of making the PVA-based resin layer contain the first and second compounds is preferably performed after dyeing the PVA-based resin layer with iodine, and more preferably performed simultaneously with the crosslinking process after dyeing. According to such a method, the hue change is small, and the influence on the optical properties of the polarizing element can be reduced.

[0026] In order to incorporate the first compound and the second compound into the polarizing element, they may be added both during the manufacture of the polarizing element and to the adhesive. Alternatively, one of the first compound and the second compound may be incorporated during the manufacture of the polarizing element and both may be incorporated into the adhesive.

[0027] (1st compound) The first compound is at least one selected from the group consisting of urea, urea derivatives, thiourea, and thiourea derivatives. The first compound can be used alone or in combination of two or more. There are water-soluble and poorly water-soluble first compounds, and either type of first compound can be used. When a poorly water-soluble first compound is used in a water-soluble adhesive, it is preferable to devise a dispersion method so that an increase in haze does not occur after the adhesive layer is formed.

[0028] (urea derivative) A urea derivative is a compound in which at least one of the four hydrogen atoms of a urea molecule is substituted with a substituent. In this case, the substituent is not particularly limited, but is preferably a substituent consisting of a carbon atom, a hydrogen atom, and an oxygen atom.

[0029] Specific examples of urea derivatives include mono-substituted ureas such as methylurea, ethylurea, propylurea, butylurea, isobutylurea, N-octadecylurea, 2-hydroxyethylurea, hydroxyurea, acetylurea, allylurea, 2-propynylurea, cyclohexylurea, phenylurea, 3-hydroxyphenylurea, (4-methoxyphenyl)urea, benzylurea, benzoylurea, o-tolylurea, and p-tolylurea.

[0030] Disubstituted ureas include 1,1-dimethylurea, 1,3-dimethylurea, 1,1-diethylurea, 1,3-diethylurea, 1,3-bis(hydroxymethyl)urea, 1,3-tert-butylurea, 1,3-dicyclohexylurea, 1,3-diphenylurea, 1,3-bis(4-methoxyphenyl)urea, 1-acetyl-3-methylurea, 2-imidazolidinone (ethylene urea), and tetrahydro-2-pyrimidinone (propylene urea).

[0031] Examples of 4-substituted ureas include tetramethylurea, 1,1,3,3-tetraethylurea, 1,1,3,3-tetrabutylurea, 1,3-dimethoxy-1,3-dimethylurea, 1,3-dimethyl-2-imidazolidinone, and 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone.

[0032] (Thiourea derivatives) A thiourea derivative is a compound in which at least one of the four hydrogen atoms of a thiourea molecule is substituted with a substituent. In this case, the substituent is not particularly limited, but is preferably a substituent consisting of a carbon atom, a hydrogen atom, and an oxygen atom.

[0033] Specific examples of thiourea derivatives include mono-substituted thioureas such as N-methylthiourea, ethylthiourea, propylthiourea, isopropylthiourea, 1-butylthiourea, cyclohexylthiourea, N-acetylthiourea, N-allylthiourea, (2-methoxyethyl)thiourea, N-phenylthiourea, (4-methoxyphenyl)thiourea, N-(2-methoxyphenyl)thiourea, N-(1-naphthyl)thiourea, (2-pyridyl)thiourea, o-tolylthiourea, and p-tolylthiourea.

[0034] Examples of the disubstituted thiourea include 1,1-dimethylthiourea, 1,3-dimethylthiourea, 1,1-diethylthiourea, 1,3-diethylthiourea, 1,3-dibutylthiourea, 1,3-diisopropylthiourea, 1,3-dicyclohexylthiourea, N,N-diphenylthiourea, N,N'-diphenylthiourea, 1,3-di(o-tolyl)thiourea, 1,3-di(p-tolyl)thiourea, 1-benzyl-3-phenylthiourea, 1-methyl-3-phenylthiourea, N-allyl-N'-(2-hydroxyethyl)thiourea, and ethylenethiourea.

[0035] An example of the 3-substituted thiourea is trimethylthiourea, and an example of the 4-substituted thiourea is tetramethylthiourea or 1,1,3,3-tetraethylthiourea.

[0036] Among the first compounds, urea derivatives or thiourea derivatives are preferred, and urea derivatives are more preferred, in that when used in an image display device having an interlayer filling configuration, the decrease in transmittance in a high temperature environment is suppressed and the decrease in polarization degree is small (cross loss is suppressed). Among the urea derivatives, mono- or di-substituted ureas are preferred, and mono-substituted ureas are more preferred. Di-substituted ureas include 1,1-substituted ureas and 1,3-substituted ureas, and 1,3-substituted ureas are more preferred.

[0037] (Second compound) The second compound is a compound having a nitroxy radical or a nitroxide group. As the second compound, an N-oxyl compound (having a functional group of CN(-C)-O) is used from the viewpoint of having a relatively stable radical at room temperature in air. · Compounds having the formula (O · represents an oxy radical and is bonded to N.)) and known compounds can be used. Examples of the N-oxyl compound include compounds having an organic group of the following structure. The compounds having the nitroxy radical or nitroxide group may be used alone or in combination of two or more kinds. [ka] (In general formula (1), R 1 represents an oxy radical, R 2 From R 5 each independently represents a hydrogen atom or an alkyl group having 1 to 10 carbon atoms, and n represents 0 or 1.) In addition, in general formula (1), the left of the dotted line represents an optional organic group. The optional organic group contains a hydrogen atom.

[0038] Examples of the compound having the above organic group include compounds represented by the following general formulas (2) to (5). [ka] (In general formula (2), R 1 From R 5 , and n are the same as above, and R 6 represents a hydrogen atom, or an alkyl group, acyl group, or aryl group having 1 to 10 carbon atoms, and n represents 0 or 1. [ka] (In general formula (3), R 1 From R 5 , and n are the same as above, and R 7 and R 8each independently represents a hydrogen atom, or an alkyl group, an acyl group, or an aryl group having 1 to 10 carbon atoms. [ka] (In general formula (4), R 1 From R 5 , and n are the same as above, and R 9 From R 11 each independently represents a hydrogen atom, or an alkyl group having 1 to 10 carbon atoms, an acyl group, an amino group, an alkoxy group, a hydroxyl group, or an aryl group. [ka] (In general formula (5), R 1 From R 5 , and n are the same as above, and R 12 represents a hydrogen atom, or an alkyl group having 1 to 10 carbon atoms, an amino group, an alkoxy group, a hydroxyl group, or an aryl group.

[0039] In the general formulas (1) to (5), R 2 From R 5 From the viewpoint of availability, R is preferably an alkyl group having 1 to 6 carbon atoms, and more preferably an alkyl group having 1 to 3 carbon atoms. 6 is preferably a hydrogen atom or an alkyl group having 1 to 10 carbon atoms, and more preferably a hydrogen atom. 7 and R 8 are preferably independently a hydrogen atom or an alkyl group having 1 to 10 carbon atoms, and more preferably a hydrogen atom. 9 From R 11 is preferably a hydrogen atom or an alkyl group having 1 to 10 carbon atoms. 12is preferably a hydroxy group, an amino group, or an alkoxy group. In the general formulas (1) to (5), n is preferably 1 from the viewpoint of availability.

[0040] Examples of the N-oxyl compound include those described in JP 2003-64022 A, JP 11-222462 A, JP 2002-284737 A, and WO 2016 / 047655 A. As the N-oxyl compound, 4-hydroxy-2,2,6,6-tetramethylpiperidine 1-oxyl is preferably used.

[0041] Examples of the second compound include the following compounds: [ka] (In the general formula (6), R represents a hydrogen atom, or an alkyl group, an acyl group, or an aryl group having 1 to 10 carbon atoms.) [ka] [ka]

[0042] From the viewpoint of efficiently capturing radicals generated in the polyenation reaction, the second compound preferably has a molecular weight of 1000 or less, more preferably 500 or less, and even more preferably 300 or less. The lower limit of the molecular weight is not particularly limited, but may be, for example, 80.

[0043] (Feature (a)) In the case of the feature (a), the moisture content of the polarizing element is equal to or higher than the equilibrium moisture content at a temperature of 20° C. and a relative humidity of 30%, and equal to or lower than the equilibrium moisture content at a temperature of 20° C. and a relative humidity of 80%. The moisture content of the polarizing element may be higher than the equilibrium moisture content at a temperature of 20° C. and a relative humidity of 45% or 50%, and equal to or lower than the equilibrium moisture content at a temperature of 20° C. and a relative humidity of 80% or 70%. If the moisture content of the polarizing element is lower than the equilibrium moisture content at a temperature of 20° C. and a relative humidity of 30%, the polarizing element becomes less easy to handle and more likely to break. If the moisture content of the polarizing element is high, such as higher than the equilibrium moisture content at a temperature of 20° C. and a relative humidity of 45% or 50%, it is presumed that the polyenation of the PVA-based resin is likely to proceed, but in this embodiment, the adhesive layer containing the first compound and the second compound is provided, so that the polyenation of the PVA-based resin can be suppressed.

[0044] A method for checking whether the moisture content of a polarizing element is within the range of equal to or greater than the equilibrium moisture content at a temperature of 20°C and a relative humidity of 30% and equal to or less than the equilibrium moisture content at a temperature of 20°C and a relative humidity of 80% can be to store the polarizing element in an environment adjusted to the above temperature and relative humidity ranges, and if there is no change in mass for a certain period of time, it can be considered that the element has reached equilibrium with the environment. Alternatively, the equilibrium moisture content of the polarizing element in an environment adjusted to the above temperature and relative humidity ranges can be calculated in advance, and the moisture content of the polarizing element can be compared with the previously calculated equilibrium moisture content.

[0045] Methods for producing a polarizing element having a moisture content equal to or greater than the equilibrium moisture content at a temperature of 20°C and a relative humidity of 30% and equal to or less than the equilibrium moisture content at a temperature of 20°C and a relative humidity of 80% include, but are not limited to, a method in which the polarizing element is stored in an environment adjusted to the above-mentioned temperature and relative humidity range for 10 minutes to 3 hours, or a method in which the polarizing element is heated at 30°C to 90°C.

[0046] Another preferred method for producing a polarizing element having the above moisture content includes a method of storing a laminate in which a protective film is laminated on at least one surface of a polarizing element, or a polarizing plate constructed using a polarizing element, in an environment adjusted to the above temperature and relative humidity ranges for 10 minutes to 120 hours, or a method of heat treating the same at 30° C. to 90° C. When producing an image display device employing an interlayer filling configuration, an image display panel in which a polarizing plate is laminated on an image display cell may be stored for 10 minutes to 3 hours or heated at 30° C. to 90° C. in an environment adjusted to the above temperature and relative humidity ranges, and then a front plate may be attached to the image display panel.

[0047] (Feature (b)) In the case of having the characteristic (b), the moisture content of the polarizing plate is equal to or higher than the equilibrium moisture content at a temperature of 20° C. and a relative humidity of 30%, and equal to or lower than the equilibrium moisture content at a temperature of 20° C. and a relative humidity of 80%. The moisture content of the polarizing plate may be higher than the equilibrium moisture content at a temperature of 20° C. and a relative humidity of 45% or 50%, and equal to or lower than the equilibrium moisture content at a temperature of 20° C. and a relative humidity of 80% or 70%. If the moisture content of the polarizing plate is lower than the equilibrium moisture content at a temperature of 20° C. and a relative humidity of 30%, the handling property of the polarizing plate is deteriorated and the polarizing plate is easily cracked. If the moisture content of the polarizing plate is high, such as higher than the equilibrium moisture content at a temperature of 20° C. and a relative humidity of 45% or 50%, it is presumed that the polyenation of the PVA-based resin is likely to proceed, but in this embodiment, since the polarizing plate is provided with adhesive layers each containing a first compound and a second compound, the polyenation of the PVA-based resin can be suppressed.

[0048] As a method for checking whether the moisture content of a polarizing plate is within the range of equal to or greater than the equilibrium moisture content at a temperature of 20°C and a relative humidity of 30% and equal to or less than the equilibrium moisture content at a temperature of 20°C and a relative humidity of 80%, it can be stored in an environment adjusted to the above temperature and relative humidity ranges, and if there is no change in mass for a certain period of time, it can be considered that the polarizing plate has reached equilibrium with the environment. Alternatively, it can be checked by previously calculating the equilibrium moisture content of the polarizing plate in an environment adjusted to the above temperature and relative humidity ranges, and comparing the moisture content of the polarizing plate with the previously calculated equilibrium moisture content.

[0049] Methods for producing a polarizing plate having a moisture content equal to or greater than the equilibrium moisture content at a temperature of 20°C and a relative humidity of 30% and equal to or less than the equilibrium moisture content at a temperature of 20°C and a relative humidity of 80% include, but are not limited to, a method in which the polarizing plate is stored in an environment adjusted to the above-mentioned temperature and relative humidity range for 10 minutes to 3 hours, or a method in which the polarizing plate is heated at 30°C to 90°C.

[0050] When producing an image display device employing an interlayer filling configuration, an image display panel having a polarizing plate laminated on an image display cell may be stored in an environment adjusted to the above-mentioned temperature and relative humidity range for 10 minutes to 3 hours or heated to 30°C to 90°C, and then a front panel may be laminated thereto.

[0051] (Method of manufacturing polarizing element) The method for producing the polarizing element is not particularly limited, but typical methods include a method in which a PVA-based resin film that has already been wound into a roll is sent out and stretched, dyed, crosslinked, and the like to produce the polarizing element (hereinafter referred to as "production method 1"), and a method including a step of applying a coating liquid containing a PVA-based resin onto a substrate film to form a PVA-based resin layer as a coating layer, and stretching the resulting laminate (hereinafter referred to as "production method 2").

[0052] Production method 1 can include a step of uniaxially stretching a PVA-based resin film, a step of dyeing the PVA-based resin film with a dichroic dye such as iodine to adsorb the dichroic dye, a step of treating the PVA-based resin film with the adsorbed dichroic dye with an aqueous boric acid solution, and a step of washing with water after the treatment with the aqueous boric acid solution.

[0053] The swelling step is a treatment step in which the PVA-based resin film is immersed in a swelling bath. The swelling step can remove dirt and blocking agents on the surface of the PVA-based resin film, and can also suppress uneven dyeing by swelling the PVA-based resin film. A medium mainly composed of water, such as water, distilled water, or pure water, is usually used for the swelling bath. The swelling bath may contain surfactants, alcohol, or the like, as appropriate, according to a conventional method. In order to control the potassium content of the polarizing element, potassium iodide may be used in the swelling bath. In this case, the concentration of potassium iodide in the swelling bath is preferably 1.5% by mass or less, more preferably 1.0% by mass or less, and even more preferably 0.5% by mass or less.

[0054] The temperature of the swelling bath is preferably about 10° C. to about 60° C., more preferably about 15° C. to about 45° C., and even more preferably about 18° C. to about 30° C. The immersion time in the swelling bath cannot be determined in general because the degree of swelling of the PVA-based resin film is affected by the temperature of the swelling bath, but is preferably about 5 seconds to about 300 seconds, more preferably about 10 seconds to about 200 seconds, and even more preferably about 20 seconds to about 100 seconds. The swelling step may be carried out only once, or may be carried out multiple times as necessary.

[0055] The dyeing process is a treatment process in which the PVA-based resin film is immersed in a dye bath (iodine solution), and a dichroic dye such as iodine can be adsorbed and oriented on the PVA-based resin film. The iodine solution is usually preferably an aqueous iodine solution, and contains iodine and an iodide as a dissolving agent. Examples of iodides include potassium iodide, lithium iodide, sodium iodide, zinc iodide, aluminum iodide, lead iodide, copper iodide, barium iodide, calcium iodide, tin iodide, and titanium iodide. Among these, potassium iodide is preferred from the viewpoint of controlling the potassium content in the polarizing element.

[0056] The concentration of iodine in the dye bath is preferably about 0.01% by mass to about 1% by mass, more preferably about 0.02% by mass to about 0.5% by mass, and the concentration of iodide in the dye bath is preferably about 0.01% by mass to about 10% by mass, more preferably about 0.05% by mass to about 5% by mass, and even more preferably about 0.1% by mass to about 3% by mass.

[0057] The temperature of the dye bath is preferably about 10° C. to 50° C., more preferably about 15° C. to 45° C., and even more preferably about 18° C. to 30° C. The immersion time in the dye bath cannot be determined in general because the degree of dyeing of the PVA-based resin film is affected by the temperature of the dye bath, but is preferably about 10 seconds to 300 seconds, and more preferably about 20 seconds to 240 seconds. The dyeing process may be carried out only once, or may be carried out multiple times as necessary.

[0058] The crosslinking step is a treatment step in which the PVA-based resin film dyed in the dyeing step is immersed in a treatment bath (crosslinking bath) containing a boron compound, and the boron compound crosslinks the polyvinyl alcohol-based resin film, allowing iodine molecules or dye molecules to be adsorbed to the crosslinked structure. Examples of the boron compound include boric acid, borate salts, and borax. The crosslinking bath is generally an aqueous solution, but may also be a mixed solution of water and an organic solvent miscible with water. The crosslinking bath preferably contains potassium iodide from the viewpoint of controlling the potassium content in the polarizing element.

[0059] In the crosslinking bath, the concentration of the boron compound is preferably about 1% by mass to about 15% by mass, more preferably about 1.5% by mass to about 10% by mass, and more preferably about 2% by mass to about 5% by mass. When potassium iodide is used in the crosslinking bath, the concentration of potassium iodide in the crosslinking bath is preferably about 1% by mass to about 15% by mass, more preferably about 1.5% by mass to about 10% by mass, and more preferably about 2% by mass to about 5% by mass.

[0060] The temperature of the crosslinking bath is preferably about 20° C. to about 70° C., more preferably about 30° C. to about 60° C. The immersion time in the crosslinking bath cannot be determined in general because the degree of crosslinking of the PVA resin film is affected by the temperature of the crosslinking bath, but is preferably about 5 seconds to about 300 seconds, more preferably about 10 seconds to about 200 seconds. The crosslinking step may be carried out only once, or may be carried out multiple times as necessary.

[0061] The stretching process is a process for stretching the PVA-based resin film at least in one direction to a predetermined magnification. In general, the PVA-based resin film is uniaxially stretched in the conveying direction (longitudinal direction). There are no particular limitations on the stretching method, and either a wet stretching method or a dry stretching method can be used. The stretching process may be carried out only once, or may be carried out multiple times as necessary. The stretching process may be carried out at any stage in the production of a polarizing element.

[0062] The treatment bath (stretching bath) in the wet stretching method can usually use a solvent such as water or a mixed solution of water and an organic solvent miscible with water. The stretching bath preferably contains potassium iodide from the viewpoint of controlling the content of potassium in the polarizing element. When potassium iodide is used in the stretching bath, the concentration of potassium iodide in the stretching bath is preferably about 1% by mass to 15% by mass, more preferably about 2% by mass to 10% by mass, and more preferably about 3% by mass to 6% by mass. The treatment bath (stretching bath) can contain a boron compound from the viewpoint of suppressing film breakage during stretching. When a boron compound is contained, the concentration of the boron compound in the stretching bath is preferably about 1% by mass to 15% by mass, more preferably about 1.5% by mass to 10% by mass, and more preferably about 2% by mass to 5% by mass.

[0063] The temperature of the stretching bath is preferably about 25° C. to about 80° C., more preferably about 40° C. to about 75° C., and even more preferably about 50° C. to about 70° C. The immersion time in the stretching bath cannot be determined in general because the degree of stretching of the PVA-based resin film is affected by the temperature of the stretching bath, but is preferably about 10 seconds to about 800 seconds, and more preferably about 30 seconds to about 500 seconds. The stretching treatment in the wet stretching method may be performed together with one or more treatment steps of a swelling step, a dyeing step, a crosslinking step, and a washing step.

[0064] Examples of the dry stretching method include a roll-to-roll stretching method, a heated roll stretching method, a compression stretching method, etc. The dry stretching method may be carried out together with a drying step.

[0065] The total stretching ratio (cumulative stretching ratio) applied to the polyvinyl alcohol-based resin film can be appropriately set depending on the purpose, but is preferably about 2 to 7 times, more preferably about 3 to 6.8 times, and even more preferably about 3.5 to 6.5 times.

[0066] The cleaning step is a treatment step in which the polyvinyl alcohol-based resin film is immersed in a cleaning bath, and foreign matter remaining on the surface of the polyvinyl alcohol-based resin film can be removed. The cleaning bath is usually made of a medium mainly composed of water, such as water, distilled water, or pure water. In addition, from the viewpoint of controlling the potassium content in the polarizing element, it is preferable to use potassium iodide in the cleaning bath. In this case, the concentration of potassium iodide in the cleaning bath is preferably about 1% by mass or more and 10% by mass or less, more preferably about 1.5% by mass or more and 4% by mass or less, and even more preferably about 1.8% by mass or more and 3.8% by mass or less.

[0067] The temperature of the cleaning bath is preferably about 5° C. to about 50° C., more preferably about 10° C. to about 40° C., and even more preferably about 15° C. to about 30° C. The immersion time in the cleaning bath cannot be determined in general because the degree of cleaning of the PVA-based resin film is affected by the temperature of the cleaning bath, but is preferably about 1 second to about 100 seconds, more preferably about 2 seconds to about 50 seconds, and even more preferably about 3 seconds to about 20 seconds. The cleaning step may be carried out only once, or may be carried out multiple times as necessary.

[0068] The drying step is a step of drying the PVA-based resin film washed in the washing step to obtain a polarizing element. The drying can be performed by any appropriate method, for example, natural drying, air drying, or heat drying.

[0069] The manufacturing method 2 can be produced through the steps of applying a coating solution containing a PVA resin onto a substrate film, uniaxially stretching the resulting laminated film, dyeing the PVA resin layer of the uniaxially stretched laminated film with a dichroic dye to adsorb it to form a polarizing element, treating the film with the adsorbed dichroic dye with an aqueous boric acid solution, and washing with water after the treatment with the aqueous boric acid solution. The substrate film used to form the polarizing element may be used as a protective layer for the polarizing element. If necessary, the substrate film may be peeled off and removed from the polarizing element.

[0070] <Transparent protective film> The first transparent protective film used in this embodiment is attached to one surface of the polarizing element via a first adhesive layer, and the second transparent protective film is attached to the other surface of the polarizing element via a second adhesive layer. Hereinafter, when it is not limited to either the first transparent protective film or the second transparent protective film, it may be simply referred to as a "protective film".

[0071] The protective film may have other optical functions at the same time, and may be formed into a laminated structure in which multiple layers are laminated. The thickness of the protective film is preferably thin from the viewpoint of optical properties, but if it is too thin, the strength decreases and the processability is poor. The appropriate thickness is 5 μm or more and 100 μm or less, preferably 10 μm or more and 80 μm or less, and more preferably 15 μm or more and 70 μm or less.

[0072] The protective film may be a cellulose acylate film, a film made of a polycarbonate resin, a film made of a cycloolefin resin such as norbornene, a (meth)acrylic polymer film, a polyester resin film such as polyethylene terephthalate, etc. When a protective film is attached to both sides of a polarizing element using a water-based adhesive such as a PVA adhesive, it is preferable that the protective film on at least one side is either a cellulose acylate film or a (meth)acrylic polymer film in terms of moisture permeability, and among these, a cellulose acylate film is preferable.

[0073] At least one of the protective films may have a retardation function for the purpose of compensating for a viewing angle. In that case, the protective film itself may have a retardation function, may have a separate retardation layer, or may be a combination of both. The film having a retardation function may be directly attached to the polarizing element via an adhesive, or may be attached via a pressure-sensitive adhesive or adhesive via another protective film attached to the polarizing element.

[0074] <Adhesive layer> An adhesive containing a first compound is used as a first adhesive constituting a first adhesive layer for bonding a first transparent protective film to a polarizing element. An adhesive containing a second compound is used as a second adhesive constituting a second adhesive layer for bonding a second transparent protective film to a polarizing element. Hereinafter, when not limited to either the first adhesive or the second adhesive, it may be simply referred to as "adhesive". Also, when not limited to either the first adhesive layer or the second adhesive layer, it may be simply referred to as "adhesive layer". The adhesive may be a water-based adhesive, a solvent-based adhesive, an active energy ray curable adhesive, or the like, but is preferably a water-based adhesive and preferably contains a PVA-based resin. By using the first adhesive containing the first compound and the second adhesive containing the second compound, it is possible to suppress the decrease in transmittance of the polarizing plate in a high temperature environment.

[0075] The thickness of the adhesive when applied can be set to any value, for example, so that an adhesive layer having a desired thickness is obtained after curing or heating (drying). The thickness of the adhesive layer made of the adhesive is preferably 0.01 μm or more and 7 μm or less, more preferably 0.01 μm or more and 5 μm or less, even more preferably 0.01 μm or more and 2 μm or less, and most preferably 0.01 μm or more and 1 μm or less.

[0076] The following description of the adhesive is a description of the preferred range in the case where the first compound and the second compound are not contained in the polarizing element during the manufacturing of the polarizing element. When the first compound and the second compound are contained in the polarizing element, the following values ​​may be appropriately adjusted. Specific examples of the first compound and the second compound are as described above. In the process of forming an adhesive layer through a drying process during adhesion between the polarizing element and the protective film, a part of the first compound and a part of the second compound may migrate from the adhesive layer to the polarizing element, etc.

[0077] When the first adhesive is an aqueous adhesive containing a PVA resin, the content of the first compound is preferably 0.1 parts by mass or more and 400 parts by mass or less, more preferably 1 part by mass or more and 200 parts by mass or less, and even more preferably 3 parts by mass or more and 100 parts by mass or less, relative to 100 parts by mass of the PVA resin. If the content is less than 0.1 parts by mass, the effect of suppressing the polyenization of the polarizing element in a high-temperature environment may not be sufficient. On the other hand, if the content exceeds 400 parts by mass, urea may precipitate after the polarizing plate is produced, and the haze may increase.

[0078] When the second adhesive is a water-based adhesive containing a PVA resin, the content of the second compound is preferably 0.1 parts by mass or more and 400 parts by mass or less, more preferably 1 part by mass or more and 200 parts by mass or less, and even more preferably 3 parts by mass or more and 100 parts by mass or less, relative to 100 parts by mass of the PVA resin. If it is less than 0.1 parts by mass, the effect of suppressing the polyenization of the polarizing element in a high-temperature environment may not be sufficient. On the other hand, if it exceeds 400 parts by mass, the second compound may precipitate after the polarizing plate is produced.

[0079] (Water-based adhesive) As the aqueous adhesive, any suitable aqueous adhesive may be used, but preferably, an aqueous adhesive containing a PVA resin (PVA adhesive) is used. From the viewpoint of adhesiveness, the average polymerization degree of the PVA resin contained in the aqueous adhesive is preferably about 100 to 5500, more preferably 1000 to 4500. From the viewpoint of adhesiveness, the average saponification degree is preferably about 85 mol% to 100 mol%, more preferably 90 mol% to 100 mol%.

[0080] The PVA resin contained in the aqueous adhesive is preferably one containing an acetoacetyl group, because it has excellent adhesion between the PVA resin layer and the protective film and excellent durability. The acetoacetyl group-containing PVA resin can be obtained, for example, by reacting a PVA resin with diketene by any method. The acetoacetyl group modification degree of the acetoacetyl group-containing PVA resin is typically 0.1 mol% or more, preferably about 0.1 mol% or more and 20 mol% or less. The resin concentration of the aqueous adhesive is preferably 0.1 mass% or more and 15 mass% or less, more preferably 0.5 mass% or more and 10 mass% or less.

[0081] The water-based adhesive may contain a crosslinking agent. Known crosslinking agents may be used as the crosslinking agent. Examples of the crosslinking agent include water-soluble epoxy compounds, dialdehydes, and isocyanates.

[0082] When the PVA-based resin is an acetoacetyl group-containing PVA-based resin, the crosslinking agent is preferably any one of glyoxal, glyoxylate, and methylolmelamine, more preferably any one of glyoxal and glyoxylate, and particularly preferably glyoxal.

[0083] The aqueous adhesive may also contain an organic solvent. The organic solvent is preferably an alcohol in terms of its miscibility with water, and among alcohols, methanol or ethanol is more preferable. The concentration of methanol in the aqueous adhesive is preferably 10% by mass or more and 70% by mass or less, more preferably 15% by mass or more and 60% by mass or less, and even more preferably 20% by mass or more and 60% by mass or less. By having a methanol concentration of 10% by mass or more, it is easier to suppress polyenation of the PVA resin in a high-temperature environment. In addition, by having a methanol content of 70% by mass or less, it is possible to suppress deterioration of the hue. Some urea derivatives have low solubility in water, but have sufficient solubility in alcohol. In that case, one of the preferred embodiments is to dissolve the first compound in alcohol to prepare an alcohol solution of the first compound, and then add the alcohol solution of the first compound to the PVA aqueous solution to prepare the first adhesive.

[0084] (Active energy ray curing adhesive) The active energy ray curable adhesive is an adhesive that is cured by irradiation with active energy rays such as ultraviolet rays, and examples thereof include an adhesive containing a polymerizable compound and a photopolymerization initiator, an adhesive containing a photoreactive resin, and an adhesive containing a binder resin and a photoreactive crosslinking agent. Examples of the polymerizable compound include photopolymerizable monomers such as photocurable epoxy monomers, photocurable acrylic monomers, and photocurable urethane monomers, and oligomers derived from these monomers. Examples of the photopolymerization initiator include compounds containing a substance that generates active species such as neutral radicals, anion radicals, and cation radicals when irradiated with active energy rays such as ultraviolet rays.

[0085] <Urea-based compound-containing layer> The first compound and the second compound are not limited to being contained in the adhesive layer as described above, and may be contained in layers other than the adhesive layer from the viewpoint of improving the high temperature durability of the polarizing plate. A cured layer may be laminated from the viewpoint of improving the physical strength of the polarizing plate.

[0086] In this embodiment, such a cured layer may contain a first compound and a second compound to form a layer containing a urea-based compound. Usually, such a cured layer is formed from a curable composition containing an organic solvent, but paragraphs

[0020] to

[0042] of JP2017-075986A disclose a method for forming such a cured layer from an aqueous solution of an active energy ray-curable polymer composition. Water-soluble first and second compounds may be contained in such a composition.

[0087] The urea compound-containing layer preferably contains at least one first compound, at least one second compound, and a binder. Examples of the binder include a polymer binder, a thermosetting resin binder, and an active energy ray-curable resin binder, and any of these binders can be preferably used.

[0088] The thickness of the urea compound-containing layer is preferably 0.1 μm or more and 20 μm or less, more preferably 0.5 μm or more and 15 μm or less, and further preferably 1 μm or more and 10 μm or less.

[0089] [Method of manufacturing polarizing plate] The manufacturing method of the polarizing plate of this embodiment includes a lamination step. The manufacturing method of the polarizing plate of this embodiment may include a moisture content adjustment step. In the moisture content adjustment step, when a polarizing plate having the characteristic (a) is manufactured, the moisture content of the polarizing element is adjusted so that the moisture content of the polarizing element is equal to or higher than the equilibrium moisture content at a temperature of 20° C. and a relative humidity of 30% and equal to or lower than the equilibrium moisture content at a temperature of 20° C. and a relative humidity of 80%. The moisture content of the polarizing element can be adjusted according to the description of the moisture content of the polarizing element described above. In the moisture content adjustment step, when a polarizing plate having the characteristic (b) is manufactured, the moisture content of the polarizing plate is adjusted so that the moisture content of the polarizing plate is equal to or higher than the equilibrium moisture content at a temperature of 20° C. and a relative humidity of 30% and equal to or lower than the equilibrium moisture content at a temperature of 20° C. and a relative humidity of 80%. The moisture content of the polarizing plate can be adjusted according to the description of the moisture content of the polarizing plate described above. In the lamination step, the polarizing element and the transparent protective film are laminated via the adhesive layer. In the lamination step, for example, a polarizing element that has not been treated to contain the first compound and the second compound and a transparent protective film are bonded together with an adhesive containing the first compound and the second compound. The order of the moisture content adjustment step and the lamination step is not limited, and the moisture content adjustment step and the lamination step may be performed in parallel.

[0090] [Image display device configuration] The polarizing plate of the present embodiment is used in various image display devices such as liquid crystal display devices and organic EL display devices. In the case of an image display device having an interlayer filling configuration in which both sides of the polarizing plate are in contact with a layer other than an air layer, specifically a solid layer such as an adhesive layer, the transmittance is likely to decrease in a high-temperature environment. In the image display device using the polarizing plate of the present embodiment, even if the interlayer filling configuration is used, the decrease in the transmittance of the polarizing plate in a high-temperature environment can be suppressed. An example of the image display device is a configuration having an image display cell, a first adhesive layer laminated on the viewing side surface of the image display cell, and a polarizing plate laminated on the viewing side surface of the first adhesive layer. Such an image display device may further have a second adhesive layer laminated on the viewing side surface of the polarizing plate and a transparent member laminated on the surface of the second adhesive layer. In particular, the polarizing plate of the present embodiment is suitably used in an image display device having an interlayer filling configuration in which a transparent member is arranged on the viewing side of the image display device, the polarizing plate and the image display cell are bonded together by the first adhesive layer, and the polarizing plate and the transparent member are bonded together by the second adhesive layer. In this specification, either or both of the first pressure-sensitive adhesive layer and the second pressure-sensitive adhesive layer may be simply referred to as an “adhesive layer.” Note that the member used for bonding the polarizing plate and the image display cell, and the member used for bonding the polarizing plate and the transparent member are not limited to a pressure-sensitive adhesive layer, and may be an adhesive layer.

[0091] <Image display cell> Examples of the image display cell include a liquid crystal cell and an organic EL cell. The liquid crystal cell may be a reflective liquid crystal cell that uses external light, a transmissive liquid crystal cell that uses light from a light source such as a backlight, or a semi-transmissive semi-reflective liquid crystal cell that uses both external light and light from a light source. When the liquid crystal cell uses light from a light source, the image display device (liquid crystal display device) has a polarizing plate disposed on the opposite side to the viewing side of the image display cell (liquid crystal cell), and further has a light source disposed thereon. The polarizing plate on the light source side and the liquid crystal cell are preferably bonded together via an appropriate adhesive layer. The driving method of the liquid crystal cell may be any type, such as VA mode, IPS mode, TN mode, STN mode, or bend orientation (π type).

[0092] As the organic EL cell, a light-emitting body (organic electroluminescence light-emitting body) is preferably formed by sequentially laminating a transparent electrode, an organic light-emitting layer, and a metal electrode on a transparent substrate. The organic light-emitting layer is a laminate of various organic thin films, and various layer configurations can be adopted, such as a laminate of a hole injection layer made of a triphenylamine derivative or the like and a light-emitting layer made of a fluorescent organic solid such as anthracene, a laminate of such a light-emitting layer and an electron injection layer made of a perylene derivative or the like, or a laminate of a hole injection layer, a light-emitting layer, and an electron injection layer.

[0093] <Laminating the image display cell and the polarizing plate> A pressure-sensitive adhesive layer (pressure-sensitive adhesive sheet) is preferably used for bonding the image display cell and the polarizing plate. Among them, a method of bonding a polarizing plate with a pressure-sensitive adhesive layer, in which a pressure-sensitive adhesive layer is attached to one side of the polarizing plate, to the image display cell is preferred from the viewpoint of workability and the like. The pressure-sensitive adhesive layer can be attached to the polarizing plate by a suitable method. Examples of such a method include a method of preparing a pressure-sensitive adhesive solution of about 10% by mass to 40% by mass by dissolving or dispersing a base polymer or a composition thereof in a solvent consisting of a single or mixture of suitable solvents such as toluene and ethyl acetate, and directly attaching the solution to the polarizing plate by a suitable spreading method such as a casting method or a coating method, and a method of forming a pressure-sensitive adhesive layer on a separator and transferring the solution to the polarizing plate.

[0094] <Adhesive layer> The adhesive layer may be composed of one layer or two or more layers, but is preferably composed of one layer. The adhesive layer may be composed of an adhesive composition mainly composed of (meth)acrylic resin, rubber resin, urethane resin, ester resin, silicone resin, or polyvinyl ether resin. Among them, an adhesive composition having a (meth)acrylic resin as a base polymer, which is excellent in transparency, weather resistance, heat resistance, etc., is preferable. The adhesive composition may be of an active energy ray curing type or a heat curing type.

[0095] As the (meth)acrylic resin (base polymer) used in the pressure-sensitive adhesive composition, a polymer or copolymer containing one or more monomers of (meth)acrylic acid esters such as butyl (meth)acrylate, ethyl (meth)acrylate, isooctyl (meth)acrylate, 2-ethylhexyl (meth)acrylate, etc. is preferably used. A polar monomer is preferably copolymerized in the base polymer. Examples of the polar monomer include monomers having a carboxyl group, a hydroxyl group, an amide group, an amino group, an epoxy group, etc., such as a (meth)acrylic acid compound, a 2-hydroxypropyl (meth)acrylate compound, a hydroxyethyl (meth)acrylate compound, a (meth)acrylamide compound, an N,N-dimethylaminoethyl (meth)acrylate compound, and a glycidyl (meth)acrylate compound.

[0096] The adhesive composition may contain only the base polymer, but usually further contains a crosslinking agent. Examples of the crosslinking agent include a divalent or higher metal ion that forms a carboxylate metal salt with a carboxyl group, a polyamine compound that forms an amide bond with a carboxyl group, a polyepoxy compound or polyol that forms an ester bond with a carboxyl group, and a polyisocyanate compound that forms an amide bond with a carboxyl group. Among them, a polyisocyanate compound is preferred.

[0097] The active energy ray curable adhesive composition has a property of being cured by irradiation with active energy rays such as ultraviolet rays and electron beams, and has a property of being able to adhere to an adherend such as a film even before irradiation with active energy rays, and is able to adjust the adhesive strength by being cured by irradiation with active energy rays. The active energy ray curable adhesive composition is preferably an ultraviolet ray curable type. The active energy ray curable adhesive composition further contains an active energy ray polymerizable compound in addition to a base polymer and a crosslinking agent. If necessary, a photopolymerization initiator, a photosensitizer, etc. may be contained.

[0098] The pressure-sensitive adhesive composition can contain additives such as microparticles for imparting light scattering properties, beads (resin beads, glass beads, etc.), glass fibers, resins other than the base polymer, tackifiers, fillers (metal powders and other inorganic powders, etc.), antioxidants, UV absorbers, dyes, pigments, colorants, defoamers, corrosion inhibitors, and photopolymerization initiators.

[0099] The adhesive layer can be formed by applying an organic solvent dilution of the adhesive composition onto the surface of a substrate film, an image display cell or a polarizing plate, and drying it.The substrate film is generally a thermoplastic resin film, and a typical example thereof is a release-treated separate film.The separate film can be, for example, a film made of a resin such as polyethylene terephthalate, polybutylene terephthalate, polycarbonate, polyarene, etc., and the surface on which the adhesive layer is formed is subjected to a release treatment such as silicone treatment.

[0100] The pressure-sensitive adhesive composition may be directly applied to the release-treated surface of the separate film to form a pressure-sensitive adhesive layer, and the pressure-sensitive adhesive layer with the separate film may be laminated on the surface of the polarizer.The pressure-sensitive adhesive composition may be directly applied to the surface of the polarizing plate to form a pressure-sensitive adhesive layer, and the separate film may be laminated on the outer surface of the pressure-sensitive adhesive layer.

[0101] When providing the pressure-sensitive adhesive layer on the surface of the polarizing plate, it is preferable to subject the bonding surface of the polarizing plate and / or the bonding surface of the pressure-sensitive adhesive layer to a surface activation treatment such as plasma treatment or corona treatment, and it is more preferable to subject the layer to corona treatment.

[0102] Alternatively, a pressure-sensitive adhesive composition may be applied onto a second separate film to form a pressure-sensitive adhesive layer, a separate film may be laminated onto the formed pressure-sensitive adhesive layer to prepare a pressure-sensitive adhesive sheet, and the pressure-sensitive adhesive layer with the separate film after peeling the second separate film from the pressure-sensitive adhesive sheet may be laminated onto a polarizing plate. The second separate film used has a weaker adhesion to the pressure-sensitive adhesive layer than the separate film and is therefore easier to peel off.

[0103] The thickness of the pressure-sensitive adhesive layer is not particularly limited, but is, for example, preferably from 1 μm to 100 μm, more preferably from 3 μm to 50 μm, and may be 20 μm or more.

[0104] <Transparent material> Examples of the transparent member arranged on the viewing side of the image display device include a transparent plate (window layer) and a touch panel. As the transparent plate, a transparent plate having appropriate mechanical strength and thickness is used. Examples of such transparent plates include transparent resin plates such as polyimide resin, acrylic resin, and polycarbonate resin, and glass plates. A functional layer such as an anti-reflection layer may be laminated on the viewing side of the transparent plate. In addition, when the transparent plate is a transparent resin plate, a hard coat layer may be laminated to increase physical strength, or a low moisture permeable layer may be laminated to reduce moisture permeability. As the touch panel, various touch panels such as resistive film type, capacitive type, optical type, and ultrasonic type, and glass plate or transparent resin plate having a touch sensor function are used. When a capacitive type touch panel is used as the transparent member, it is preferable that a transparent plate made of glass or transparent resin plate is provided on the viewing side further than the touch panel.

[0105] <Laminating a polarizing plate to a transparent material> A pressure sensitive adhesive or an active energy ray curable adhesive is preferably used for bonding the polarizing plate and the transparent member. When a pressure sensitive adhesive is used, the pressure sensitive adhesive can be applied by an appropriate method. As a specific application method, for example, the application method of the pressure sensitive adhesive layer used for bonding the image display cell and the polarizing plate described above can be mentioned.

[0106] When an active energy ray curable adhesive is used, a method is preferably used in which a dam material is provided around the periphery of the image display panel in order to prevent the adhesive solution from spreading before curing, a transparent member is placed on the dam material, and the adhesive solution is then poured in. After the adhesive solution is poured, alignment and degassing are performed as necessary, and then the adhesive solution is irradiated with active energy rays to cause curing. EXAMPLES

[0107] The present invention will be specifically described below based on examples. The materials, reagents, amounts of substances and their ratios, operations, etc. shown in the following examples can be appropriately changed without departing from the spirit of the present invention. Therefore, the present invention is not limited to the following examples.

[0108] <Preparation of Polarizing Element A> A 40 μm thick PVA film made of PVA with an average degree of polymerization of about 2400 and a degree of saponification of 99.9 mol% or more was uniaxially stretched by about 5 times in a dry state, and then immersed in pure water at 60° C. for 1 minute while maintaining tension, and then immersed in an aqueous solution with a weight ratio of iodine / potassium iodide / water of 0.05 / 5 / 100 at 28° C. for 60 seconds. Then, immersed in an aqueous solution with a weight ratio of potassium iodide / boric acid / water of 8.5 / 8.5 / 100 at 72° C. for 300 seconds. Then, washed with pure water at 26° C. for 20 seconds, and dried at 65° C. to obtain a polarizing element A with a thickness of 15 μm in which iodine was adsorbed and aligned in the PVA. A digital micrometer “MH-15M” manufactured by Nikon Corporation was used to measure the thickness of the polarizing element.

[0109] <Preparation of adhesive> (Preparation of PVA solution A for adhesive) 50 g of a modified PVA resin containing acetoacetyl groups ("Gohsenex Z-410" manufactured by Mitsubishi Chemical Corporation) was dissolved in 950 g of pure water, heated at 90°C for 2 hours, and then cooled to room temperature to obtain a PVA solution for adhesive (hereinafter referred to as "PVA solution A").

[0110] (Preparation of Adhesives 1a, 1b, 1c, 2a, 2b, 2c, 3) Each adhesive was prepared by mixing PVA solution A, urea as the first compound, 4-hydroxy-2,2,6,6-tetramethylpiperidine 1-oxyl (hereinafter also referred to as "TEMPOL") as the second compound, and pure water so that PVA solution A was 3.0 mass % and the contents of the first compound and second compound were as shown in Table 1.

[0111] [Table 1]

[0112] <Preparing transparent protective film A> A commercially available cellulose acylate film TD40 (manufactured by Fujifilm Corporation, film thickness 40 μm) was immersed in a 1.5 mol / L NaOH aqueous solution (saponification solution) kept at 55° C. for 2 minutes, and then washed with water. After that, it was immersed in a 0.05 mol / L sulfuric acid aqueous solution at 25° C. for 30 seconds, and then passed through a water washing bath under running water for 30 seconds to neutralize the film. Then, after removing the water by repeatedly draining it with an air knife three times, it was allowed to stay in a drying zone at 70° C. for 15 seconds and dried to prepare a saponified film, which was named transparent protective film A.

[0113] <Preparation of Polarizing Plates 1 to 8> Transparent protective film A was laminated to both sides of polarizing element A via adhesive 3 using a roll laminator, and then dried at 80°C for 5 minutes to obtain polarizing plate 1. The adhesive layer was adjusted so that the thickness after drying was 50 nm on both sides. The adhesive layer for laminating transparent protective film A to one side of polarizing element A was referred to as the first adhesive layer, and the adhesive layer for laminating transparent protective film A to the other side was referred to as the second adhesive layer.

[0114] In the polarizing plate 1, the adhesive 3 used on both sides was changed to each of the adhesives shown in Table 2, and polarizing plates 2 to 8 were obtained.

[0115] (Adjustment of moisture content of polarizing plate (polarizing element)) The polarizing plates 1 to 8 obtained above were stored for 72 hours at a temperature of 20°C and a relative humidity of 30%, 35%, 40%, 45%, 50% or 55%. The moisture content was measured using the Karl Fischer method after 66, 69 and 72 hours of storage. The moisture content did not change after 66, 69 and 72 hours of storage under any humidity condition. Therefore, the moisture content of the polarizing plates 1 to 8 can be considered to be the same as the equilibrium moisture content in the 72-hour storage environment used in this experimental example. When the moisture content of the polarizing plate reaches equilibrium in a certain storage environment, the moisture content of the polarizing element in the polarizing plate can also be considered to have reached equilibrium in that storage environment. In addition, when the moisture content of the polarizing element in the polarizing plate reaches equilibrium in a certain storage environment, the moisture content of the polarizing plate can also be considered to have reached equilibrium in that storage environment.

[0116] <Optical laminate 1~8> Optical laminates 1 to 8 were produced using any one of polarizing plates 1 to 8 shown in Table 2. The optical laminates 1 to 8 were stored for 72 hours under conditions of a temperature of 20°C and a relative humidity of 30%, 45% or 55% so that the moisture content of the polarizing plate (polarizing element) used would be the equilibrium moisture content in the environment shown in Table 2, and were subjected to the following high-temperature durability evaluation at each moisture content.

[0117] <High temperature durability evaluation> (Preparation of evaluation samples) For the optical laminates 1 to 8 in each moisture content state, an acrylic adhesive (manufactured by Lintec Corporation, product number: #7) was applied to both sides, and then the laminates were cut into pieces measuring 50 mm x 100 mm so that the absorption axis was parallel to the long side. An alkali-free glass ("EAGLE XG" manufactured by Corning Incorporated) was attached to each adhesive surface to prepare evaluation samples. In order to evaluate the cross-drop of the above evaluation sample, an acrylic adhesive (manufactured by Lintec Corporation, product number: #7) was applied to only one side of the above polarizing plate 1 in order to create a cross-Nicol state by overlapping it with the evaluation sample, and the polarizing plate was cut to a size of 50 mm x 100 mm so that the absorption axis was parallel to the short side, and alkali-free glass ("EAGLE XG" manufactured by Corning Incorporated) was bonded to the adhesive surface to prepare an optical laminate R to be used for cross evaluation.

[0118] The evaluation samples of the optical laminates 1 to 8 were subjected to a temperature of 50°C and a pressure of 5 kgf / cm 2 (490.3 kPa) for 1 hour, and then left to stand for 24 hours in an environment with a temperature of 23° C. and a relative humidity of 55%. Thereafter, the evaluation samples of the optical laminates 1 to 8 having each moisture content were subjected to a high temperature durability evaluation as follows.

[0119] (i) Evaluation sample with a polarizing plate or polarizing element having an equilibrium moisture content at a temperature of 20°C and a relative humidity of 55% (Single unit transmittance evaluation (105℃)) For evaluation samples of optical laminates 1 to 8, in which the moisture content of the polarizing plate or polarizing element is the equilibrium moisture content at a temperature of 20°C and a relative humidity of 55%, the transmittance was measured (initial value), and the samples were stored in a heated environment at a temperature of 105°C, and the transmittance was measured every 24 hours for 48 to 96 hours. Evaluation was performed according to the following criteria, based on the time at which the transmittance had decreased by 5% or more from the initial value. The results are shown in Table 2. The decrease in transmittance after 96 hours is 5% or less: A1 The transmittance drops by 5% or more after 72 to 96 hours: B1 The transmittance drops by 5% or more after 48 to 72 hours: C1 The transmittance decreases by 5% or more after 48 hours: D1

[0120] (Cross-pass evaluation) An evaluation sample was prepared after the measurement of the single transmittance after 96 hours in the above evaluation of the single transmittance. The optical laminate R for the crossed Nicols evaluation, which had not been placed in a heated environment, and the evaluation sample were arranged in a crossed Nicols relationship and placed on a backlight. The surroundings were shaded, and the cross-drop defects were visually evaluated on a four-point scale according to the following criteria. The results are shown in Table 2. Evaluation samples with a single transmittance evaluation other than A1 were excluded from the evaluation of cross-drop defects because they had coloration due to polyenation. No cross-linking is observed: A1 Almost no cross-cutting is observed: B1 Slight cross-drop: C1 Cross-drops are clearly visible: D1

[0121] (ii) An evaluation sample in which the moisture content of a polarizing plate or polarizing element is the equilibrium moisture content at a temperature of 20°C and a relative humidity of 45%. (Single unit transmittance evaluation (105℃)) For evaluation samples of optical laminates 1 to 8, in which the moisture content of the polarizing plate or polarizing element is the equilibrium moisture content at a temperature of 20°C and a relative humidity of 45%, the transmittance was measured (initial value), and the samples were stored in a heated environment at a temperature of 105°C, and the transmittance was measured every 50 hours for 100 to 200 hours. Evaluation was performed according to the following criteria, based on the time at which the transmittance had decreased by 5% or more from the initial value. The results are shown in Table 2. The decrease in transmittance after 200 hours is 5% or less: A2 The transmittance drops by 5% or more after 150 to 200 hours: B2 The transmittance drops by 5% or more after 100 to 150 hours: C2 Transmittance reduction of 5% or more after 100 hours: D2

[0122] (Cross-pass evaluation) An evaluation sample was prepared after the measurement of the single transmittance after 200 hours in the above evaluation of the single transmittance. The optical laminate R for the crossed Nicols evaluation, which had not been placed in a heating environment, and the evaluation sample were arranged in a crossed Nicols relationship and placed on a backlight. The surroundings were shaded, and the cross-drop defects were visually evaluated on a four-point scale according to the following criteria. The results are shown in Table 2. Evaluation samples with a single transmittance evaluation other than A2 were excluded from the evaluation of cross-drop defects because they had coloration due to polyenation. No cross-linking is observed: A2 Almost no cross-cutting is observed: B2 Slight cross-drop: C2 Cross-drops are clearly visible: D2

[0123] (iii) An evaluation sample in which the moisture content of a polarizing plate or polarizing element is the equilibrium moisture content at a temperature of 20°C and a relative humidity of 30%. (Single unit transmittance evaluation (105℃)) For evaluation samples of optical laminates 1 to 8, in which the moisture content of the polarizing plate or polarizing element is the equilibrium moisture content at a temperature of 20°C and a relative humidity of 30%, the transmittance was measured (initial value), and the samples were stored in a heated environment at a temperature of 105°C, and the transmittance was measured every 150 hours for 500 to 800 hours. Evaluation was performed according to the following criteria, based on the time at which the transmittance had decreased by 5% or more from the initial value. The results are shown in Table 2. The decrease in transmittance after 800 hours is 5% or less: A3 After 650-800 hours, the transmittance has decreased by 5% or more: B3 The transmittance drops by 5% or more after 500 to 650 hours: C3 Transmittance reduction of 5% or more after 500 hours: D3

[0124] (Cross-pass evaluation) An evaluation sample was prepared after the measurement of the single transmittance after 800 hours in the evaluation of the single transmittance described above. The optical laminate R for the crossed Nicols evaluation, which had not been placed in a heating environment, and the evaluation sample were arranged in a crossed Nicols relationship and placed on a backlight. The surroundings were shaded, and the cross-drop defects were visually evaluated on a four-point scale according to the following criteria. The results are shown in Table 2. Evaluation samples with a single transmittance evaluation other than A3 were excluded from the evaluation of cross-drop defects because they had coloration due to polyenation. No cross-cutting is observed: A3 Almost no cross-cutting is seen: B3 Slight cross-drop: C3 Cross-drops are clearly visible: D3

[0125] [Table 2]

[0126] Polarizing plates (optical laminates 6 to 8) in which a polarizing element and a first transparent protective film are bonded together with a first adhesive containing a first compound, and a polarizing element and a second transparent protective film are bonded together with a second adhesive containing a second compound, are resistant to a decrease in transmittance even when exposed to a high-temperature environment of 105°C, regardless of the moisture content of the polarizing plate and polarizing element, and also have excellent evaluations for cross-loss, indicating that they have excellent high-temperature durability.

Claims

1. A polarizing plate comprising: a polarizing element having a polyvinyl alcohol-based resin layer in which a dichroic dye is adsorbed and oriented; a first transparent protective film laminated on one surface of the polarizing element; and a second transparent protective film laminated on the other surface of the polarizing element, the polarizing element and the first transparent protective film are bonded to each other by a first adhesive layer formed from a first adhesive containing a first compound and not containing a second compound; the polarizing element and the second transparent protective film are bonded to each other by a second adhesive layer formed from a second adhesive containing a second compound and not containing the first compound; the first compound is urea; A polarizing plate, wherein the second compound is a compound having a nitroxy radical or a nitroxide group.

2. 2. The polarizing plate according to claim 1, wherein the second compound is an N-oxyl compound.

3. The polarizing plate according to claim 1 , wherein the first adhesive and the second adhesive contain a polyvinyl alcohol-based resin.

4. The polarizing plate according to claim 3 , wherein the content of the first compound in the first adhesive is from 0.1 parts by mass to 400 parts by mass with respect to 100 parts by mass of the polyvinyl alcohol-based resin.

5. The polarizing plate according to claim 3 , wherein the second adhesive contains the second compound in an amount of 0.1 parts by mass or more and 400 parts by mass or less with respect to 100 parts by mass of the polyvinyl alcohol-based resin.

6. 6. The polarizing plate according to claim 1, wherein the first adhesive layer and the second adhesive layer have a thickness of 0.01 μm or more and 7 μm or less.

7. The polarizing plate is used in an image display device, 7. The polarizing plate according to claim 1, wherein in the image display device, solid layers are provided on both sides of the polarizing plate in contact with each other.

8. An image display device comprising: an image display cell; a first pressure-sensitive adhesive layer laminated on a viewing side surface of the image display cell; and a polarizing plate according to any one of claims 1 to 7 laminated on the viewing side surface of the first pressure-sensitive adhesive layer.

9. The image display device according to claim 8 , further comprising: a second adhesive layer laminated on the viewer-side surface of the polarizing plate; and a transparent member laminated on the viewer-side surface of the second adhesive layer.

10. The image display device according to claim 9 , wherein the transparent member is a glass plate or a transparent resin plate.

11. The image display device according to claim 9 , wherein the transparent member is a touch panel.

12. A method for producing a polarizing plate having a polarizing element in which a dichroic dye is adsorbed and oriented in a polyvinyl alcohol-based resin layer, a first transparent protective film laminated on one surface of the polarizing element, and a second transparent protective film laminated on the other surface of the polarizing element, comprising: a lamination step of bonding the polarizing element and the first transparent protective film with a first adhesive containing a first compound and not containing a second compound; a lamination step of bonding the polarizing element and the second transparent protective film with a second adhesive containing a second compound and not containing the first compound, the first compound is urea; The second compound is a compound having a nitroxy radical or a nitroxide group.

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