JP7176829B2 - Polarizing film, optical film, and image display device - Google Patents

Description

The present invention relates to a polarizing film comprising a polarizer and an adhesive layer adjacent to the polarizer or an optical film other than the polarizer. The polarizing film can form an image display device such as a mobile phone, a car navigation device, a monitor for a personal computer, a television, or the like, either alone or as an optical film in which the polarizing film is laminated.

Liquid crystal display devices are rapidly developing in the market for mobile phones, car navigation devices, monitors for personal computers, televisions, and the like. A liquid crystal display device visualizes a polarized state by switching liquid crystal, and a polarizer is used from its display principle. In particular, in applications such as TVs, higher brightness, higher contrast, and wider viewing angles are increasingly required, and polarizing films are increasingly required to have higher transmittance, higher degree of polarization, and higher color reproducibility.

As a polarizer, since it has a high transmittance and a high degree of polarization, for example, an iodine-based polarizer having a structure in which iodine is adsorbed on polyvinyl alcohol (hereinafter also simply referred to as “PVA”) and stretched is most commonly widely used. in use. Generally, a polarizing film is obtained by laminating transparent protective films on both sides of a polarizer with a so-called water-based adhesive made by dissolving a polyvinyl alcohol-based material in water (Patent Document 1 below). As the transparent protective film, triacetyl cellulose or the like having high moisture permeability is used. When the water-based adhesive is used (so-called wet lamination), a drying step is required after bonding the polarizer and the transparent protective film.

On the other hand, active energy ray-curable adhesives have been proposed instead of the water-based adhesives. When a polarizing film is produced using an active energy ray-curable adhesive, the productivity of the polarizing film can be improved because a drying step is not required. For example, a radical polymerization type active energy ray-curable adhesive using an N-substituted amide-based monomer as a curable component has been proposed (Patent Document 2 below). The adhesive layer formed using the active energy ray-curable adhesive described in Patent Document 2 is sufficient for a water resistance test that evaluates the presence or absence of color loss and peeling after immersion in hot water at 60 ° C. for 6 hours. Clearable. However, in recent years, polarizing films are often used not only for mobile applications such as mobile phones, but also for image display devices for in-vehicle applications. You have to pass the exam.

Japanese Patent Application Laid-Open No. 2001-296427 Japanese Unexamined Patent Application Publication No. 2012-052000

As a durability test required for polarizing films used for in-vehicle use, there is, for example, a humidity durability test in which the film is exposed to an environment of 65° C.-95% humidity for 1000 hours. Here, when the inventors of the present invention examined in detail the appearance state of the polarizing film after the humidification durability test, it was found that bright spots derived from white haze-like foreign matter were generated, especially at the edges of the polarizing film, and the appearance characteristics were poor. It was found that the product was defective. Such a phenomenon was observed for the first time after a durability test in a high-temperature and high-humidity environment, and there was a need to earnestly study to find a new solution.

The present invention was developed in view of the above circumstances, and an object of the present invention is to provide a polarizing film that suppresses the generation of bright spots due to foreign matter even after a humidification durability test and has excellent appearance characteristics.

The above problems can be solved by the following configuration. That is, the present invention provides a polarizing film comprising a polarizer and an adhesive layer adjacent to the polarizer or an optical film other than the polarizer, wherein the adhesive layer is formed by a cured product layer of an adhesive composition. The adhesive composition contains 25 parts by weight or more of a monomer component having two or more polymerizable functional groups when the total amount of the monomer components is 100 parts by weight. , and a polarizing film characterized by having no bright spots originating from foreign matter beyond 3 mm from the end face after a humidification durability test in which the film is exposed to an environment of 65° C. and 95% humidity for 1000 hours.

In the polarizing film, the adhesive composition preferably contains 40 parts by weight or less of a monomer component having a hydroxyl group when the total amount of the monomer components is 100 parts by weight.

In the polarizing film, the polarizer preferably contains a metal component capable of becoming a divalent metal cation in water.

In the polarizing film, the metal component is preferably zinc.

In the polarizing film, the polarizing film is composed of a polarizer and an optical film laminated on at least one surface of the polarizer with a water-based adhesive layer interposed therebetween, and the surface of the optical film opposite to the water-based adhesive layer. It is preferable to have an adhesive layer on the inside.

In the polarizing film, it is preferable that the adhesive layer is formed of a cured product layer of an active energy ray-curable adhesive composition.

In the polarizing film, the adhesive layer is formed of a cured product layer of an adhesive composition, and the cured product obtained by curing the adhesive composition was immersed in pure water at 23°C for 24 hours. In case,
Formula: {(M2−M1)/M1}×100 (%),
However, M1: weight of cured product before immersion, M2: weight of cured product after immersion,
is less than 10% by weight.

Further, according to the present invention, there is provided an optical film comprising a laminate of at least one polarizing film according to any one of the above; It relates to an image display device characterized by:

Polarizing films used for in-vehicle applications are required to have excellent appearance characteristics even after a humidity durability test in which the film is exposed to an environment of 65° C. and 95% humidity for 1000 hours. The polarizing film according to the present invention does not have bright spots originating from foreign matter beyond 3 mm from the end face after the humidification durability test, and therefore has excellent appearance characteristics.

In particular, even when the polarizing film according to the present invention includes a polarizer containing a metal component capable of becoming a divalent metal cation in water, particularly zinc, the polarizing film has excellent appearance properties. Although the reason why this effect is obtained is not clear, the following reason can be presumed, for example.

In a polarizing film comprising a polarizer and an adhesive layer adjacent to the polarizer or an optical film other than the polarizer, during the humidification durability test, the metal component contained in the polarizer that can become a divalent metal cation in water Zinc, in particular, migrates into the adhesive layer via vapor or condensation at the edges of the polarizing film. Here, in the adhesive layer, components other than the components contained in the raw material adhesive composition, such as oxalic acid, are present in an ionized state, but do not combine with the metal component to form oxalate. As long as oxalic acid is not detected as a foreign substance in the adhesive layer. However, when a specific metal component contained in the polarizer is mixed into the adhesive layer from the edge during the humidification durability test, the ionized oxalic acid and the metal component combine to Oxalates are generated at the edges and become white bright spots, which are detected as foreign matter. As a result, the appearance properties of the polarizing film deteriorate.

In particular, when the adhesive layer provided in the polarizing film according to the present invention is formed of a cured product layer of an adhesive composition, and the adhesive composition has a total amount of monomer components of 100 parts by weight, By containing 25 parts by weight or more of a monomer component having two or more polymerizable functional groups, bonding between ionized oxalic acid and the metal component, particularly at the edges of the adhesive layer, and further at the edges of the polarizing film movement of oxalate from to the inside can be suppressed. As a result, the appearance characteristics of the polarizing film are remarkably improved even after the humidification durability test.

The polarizing film according to the present invention is a polarizing film comprising a polarizer and an adhesive layer adjacent to the polarizer or an optical film other than the polarizer, and is exposed to an environment of 65 ° C.-95% humidity for 1000 hours. After the humidification durability test, there are no bright spots originating from foreign matter beyond 3 mm from the end face. In particular, when the polarizer according to the present invention includes an adhesive layer designed so that the bulk water absorption of the cured product layer of the adhesive composition as a raw material is less than 10% by weight, the polarizer contains a specific Even if the metal component is mixed into the adhesive layer from the edge, the bonding between the ionized oxalic acid and the metal component and the movement of oxalate from the edge of the polarizing film to the inside are suppressed. . As a result, the appearance characteristics of the polarizing film are particularly improved even after the humidification durability test.

BRIEF DESCRIPTION OF THE DRAWINGS It is an example of the cross-sectional schematic diagram of the polarizing film which concerns on one Embodiment of this invention. It is another example of the cross-sectional schematic diagram of the polarizing film which concerns on one Embodiment of this invention.

An example of the cross-sectional schematic diagram of the polarizing film which concerns on FIG. 1 at one Embodiment of this invention is shown. The polarizing film 10 in this embodiment comprises a polarizer 1 and an adhesive layer 5 adjacent to the first optical film 4 other than the polarizer 1 . More specifically, a polarizer 1 and a first optical film (retardation film) 4 are laminated on at least one surface of the polarizer 1 with a water-based adhesive layer 2 interposed therebetween. An adhesive layer 5 is provided on the side opposite to the adhesive layer 2 . In particular, in the polarizing film 10 of this embodiment, a second optical film (transparent protective film) 3 is laminated on one surface of the polarizer 1 via a water-based adhesive layer 2, and the other surface of the polarizer 1 has a water-based adhesive layer. A first optical film (retardation film) 4 is laminated via an adhesive layer 2 , an adhesive layer 5 is laminated on the first optical film (retardation film) 4 , and a third film is laminated on the adhesive layer 5 . An optical film (retardation film) 6 is laminated. The polarizing film 10 is further laminated with an adhesive layer 7 on the third optical film 6 , and is laminated on an image display cell or the like via the adhesive layer 7 .

FIG. 2 shows another example of a schematic cross-sectional view of the polarizing film according to one embodiment of the present invention. The polarizing film 10 in this embodiment comprises a polarizer 1 and an adhesive layer 5 adjacent to the polarizer 1 . More specifically, in the polarizing film 10 of this embodiment, a second optical film (transparent protective film) 3 is laminated on one surface of the polarizer 1 with a water-based adhesive layer 2 interposed therebetween, and the other surface of the polarizer 1 A first optical film (retardation film) 4 is laminated on the surface of the substrate with an adhesive layer 5 interposed therebetween. The polarizing film 10 is further laminated with an adhesive layer 7 on the optical film 4 , and is laminated on an image display cell or the like via the adhesive layer 7 .

In the polarizing film shown in FIGS. 1 and 2, the water-based adhesive layer 2 is an aqueous solution (for example, a solid concentration of 0.5 to 60% by weight) is preferably used. The thickness of the water-based adhesive layer 2 is not particularly limited, but is usually about 0.01 μm to 0.5 μm after drying.

In the polarizing film 10 shown in FIGS. 1 and 2, during the humidification durability test, the metal component contained in the polarizer 1 that can become a divalent metal cation in water, particularly zinc, vaporized at the edge of the polarizing film 10. It moves into the adhesive layer 5 via dew condensation. Here, in the adhesive layer 5, components other than the components contained in the raw material adhesive composition, such as oxalic acid, are present in an ionized state, but are combined with the metal component to form oxalate. Oxalic acid is not detectable as a contaminant in the adhesive layer unless Here, when a specific metal component contained in the polarizer 10 is mixed into the adhesive layer 5 during the humidification durability test, the ionized oxalic acid and the metal component combine to generate oxalate, Although it becomes a white bright spot and is detected as a foreign matter, the polarizing film 10 shown in FIGS. More than, more preferably more than 2 mm from the end face, it does not have bright spots originating from foreign matter.

Each configuration of the polarizing film according to the present invention will be described below. In the present invention, the polarizing film includes a polarizer and an adhesive layer adjacent to the polarizer or an optical film other than the polarizer.

<Polarizer>
Polyvinyl alcohol or a derivative thereof is used as the material of the polyvinyl alcohol film applied to the polarizer. Derivatives of polyvinyl alcohol include polyvinyl formal, polyvinyl acetal and the like, and those modified with olefins such as ethylene and propylene, alkyl esters of unsaturated carboxylic acids such as acrylic acid, methacrylic acid and crotonic acid, and acrylamide. mentioned. Generally used polyvinyl alcohol has a degree of polymerization of about 1000 to 10000 and a degree of saponification of about 80 to 100 mol %.

The polyvinyl alcohol-based film may contain additives such as plasticizers. Examples of plasticizers include polyols and condensates thereof, such as glycerin, diglycerin, triglycerin, ethylene glycol, propylene glycol, and polyethylene glycol. The amount of the plasticizer to be used is not particularly limited, but is preferably 20% by weight or less in the polyvinyl alcohol film.

In the production of the polarizer, a dyeing step of dyeing the polyvinyl alcohol film with iodine and a stretching step of stretching the polyvinyl alcohol film in at least one direction are performed. In general, a method is employed in which the polyvinyl alcohol film is subjected to a series of steps including swelling, dyeing, cross-linking, stretching, washing with water and drying.

The swelling step is performed, for example, by immersing the polyvinyl alcohol-based film in a swelling bath (water bath). This treatment removes stains and antiblocking agents from the surface of the polyvinyl alcohol-based film, and swells the polyvinyl alcohol-based film, thereby preventing non-uniformity such as uneven dyeing. Glycerin, potassium iodide, or the like may be appropriately added to the swelling bath. The temperature of the swelling bath is usually about 20 to 60° C., and the immersion time in the swelling bath is usually about 0.1 to 10 minutes.

The dyeing step is performed, for example, by immersing the polyvinyl alcohol film in an iodine solution. The iodine solution is usually an aqueous iodine solution containing iodine and potassium iodide as a solubilizing agent. The iodine concentration is usually about 0.01 to 1% by weight, preferably 0.02 to 0.5% by weight. The potassium iodide concentration is usually about 0.01 to 10% by weight, preferably 0.02 to 8% by weight.

In the iodine dyeing step, the temperature of the iodine solution is usually about 20-50°C, preferably 25-40°C. The immersion time is usually about 10 to 300 seconds, preferably 20 to 240 seconds. In the iodine dyeing treatment, conditions such as the concentration of the iodine solution, the immersion temperature of the polyvinyl alcohol film in the iodine solution, and the immersion time, etc., so that the iodine content and the potassium content in the polyvinyl alcohol film are within the above ranges. is preferably adjusted.

The cross-linking step is performed, for example, by immersing the iodine-dyed polyvinyl alcohol-based film in a treatment bath containing a cross-linking agent. Any appropriate cross-linking agent is employed as the cross-linking agent. Specific examples of cross-linking agents include boron compounds such as boric acid and borax, glyoxal, and glutaraldehyde. These are used alone or in combination. Water is generally used as a solvent for the solution of the cross-linking bath, but an appropriate amount of an organic solvent compatible with water may be added. The cross-linking agent is generally used in a proportion of 1 to 10 parts by weight per 100 parts by weight of the solvent. It is desirable that the cross-linking bath solution further contains an auxiliary agent such as iodide. The concentration of the auxiliary agent is preferably 0.05-15% by weight, more preferably 0.5-8% by weight. The temperature of the cross-linking bath is usually about 20 to 70°C, preferably 40 to 60°C. The immersion time in the cross-linking bath is usually about 1 second to 15 minutes, preferably 5 seconds to 10 minutes.

The stretching step is a step in which the polyvinyl alcohol film is stretched in at least one direction. Generally, a polyvinyl alcohol film is uniaxially stretched in the transport direction (longitudinal direction). The stretching method is not particularly limited, and either a wet stretching method or a dry stretching method can be employed. When the wet stretching method is employed, the polyvinyl alcohol film is stretched to a predetermined magnification in the treatment bath. As a solution for the stretching bath, a solution in which a compound necessary for various treatments is added to a solvent such as water or an organic solvent (eg, ethanol) is preferably used. Examples of the dry drawing method include a roll-to-roll drawing method, a heated roll drawing method, a compression drawing method, and the like. The stretching process may be performed at any stage in the production of the polarizer. Specifically, it may be carried out simultaneously with swelling, dyeing and crosslinking, or may be carried out before or after each of these steps. Also, the stretching may be performed in multiple stages. The cumulative draw ratio of the polyvinyl alcohol film is usually 5 times or more, preferably about 5 to 7 times.

In the present invention, the polarizer preferably contains a metal component that can become a divalent metal cation in water, more preferably magnesium, calcium, copper or zinc, and particularly preferably zinc. . When the polarizer contains zinc, the decrease in transmittance and the deterioration in hue of the polarizing film after the heating test tend to be suppressed. When the polarizer contains zinc, the content of zinc in the polarizer is preferably 0.002 to 2% by weight, more preferably 0.01 to 1% by weight.

In the present invention, the polarizer preferably contains sulfate ions. When the polarizer contains sulfate ions, the decrease in transmittance of the polarizing film after the heating test tends to be suppressed. When the polarizer contains sulfate ions, the content of sulfate ions in the polarizer is preferably 0.02 to 0.45% by weight, more preferably 0.05 to 0.35% by weight, and 0.1 to 0.25% by weight is more preferred. The content of sulfate ions in the polarizer is calculated from the content of sulfur atoms.

In order to contain zinc in the polarizer, it is preferable to perform zinc impregnation treatment in the manufacturing process of the polarizer. Moreover, in order to make the polarizer contain sulfate ions, it is preferable to perform sulfate ion treatment in the manufacturing process of the polarizer.

Zinc impregnation treatment is performed by, for example, immersing a polyvinyl alcohol-based film in a zinc salt solution. As the zinc salt, an aqueous inorganic salt compound such as a zinc halide such as zinc chloride or zinc iodide, zinc sulfate, or zinc acetate is suitable. Various zinc complex compounds may be used for the zinc impregnation treatment. As the zinc salt solution, it is preferable to use an aqueous solution containing potassium ions and iodine ions with potassium iodide or the like because it is easy to impregnate with zinc ions. The concentration of potassium iodide in the zinc salt solution is preferably about 0.5-10% by weight, more preferably 1-8% by weight.

Sulfate ion treatment is performed, for example, by immersing a polyvinyl alcohol-based film in an aqueous solution containing a metal sulfate. As the metal sulfate, it is preferable to use one that easily separates into sulfate ions and metal ions in the treatment liquid and that the metal sulfate is easily introduced into the polyvinyl alcohol-based film in the form of ions. For example, types of metals that form metal sulfate salts include alkali metals such as sodium and potassium; alkaline earth metals such as magnesium and calcium; transition metals such as cobalt, nickel, zinc, chromium, aluminum, copper, manganese, and iron; metals.

In the production of the polarizer, the zinc impregnation treatment and the sulfate ion treatment may be performed at any stage. That is, the zinc impregnation treatment and the sulfate ion treatment may be performed before the dyeing process or after the dyeing process. The zinc impregnation treatment and the sulfate ion treatment may be performed simultaneously. In the present invention, zinc sulfate is used as the zinc salt and the metal sulfate salt, and the zinc impregnation treatment and the sulfate ion treatment are simultaneously performed by immersing the polyvinyl alcohol film in a treatment bath containing zinc sulfate. is preferred. Alternatively, the zinc salt and/or the metal sulfate salt may coexist in the dyeing solution, and the zinc impregnation treatment and/or the sulfate ion treatment may be performed at the same time as the dyeing step. Zinc impregnation treatment and sulfate ion treatment may be performed simultaneously with stretching.

In the zinc impregnation treatment and the sulfate ion treatment, zinc in the polarizer is controlled by adjusting the concentration of the zinc salt solution and the metal sulfate solution, the temperature of immersion of the polyvinyl alcohol film in the treatment bath, and the immersion time. Content and sulfate ion content are adjusted. In the zinc impregnation treatment and sulfate ion treatment, the temperature of the zinc salt solution and the metal sulfate solution is usually about 15 to 85°C, preferably 25 to 70°C. The immersion time is usually about 1 to 120 seconds, preferably 3 to 90 seconds. The concentrations of the zinc salt solution and the metal sulfate solution vary depending on the type of zinc salt or metal sulfate, but are generally about 0.5 to 20% by weight, preferably 1 to 10% by weight, more preferably 2 to 7% by weight. %. By setting the zinc salt concentration and the metal sulfate concentration within the above ranges, the zinc content and the sulfate ion content in the polarizer can be set within the preferred ranges.

The polyvinyl alcohol film (stretched film) to which each of the above treatments has been applied is subjected to a water washing step and a drying step according to a conventional method.

The water washing step is usually carried out by immersing the polyvinyl alcohol film in a water washing bath. The washing bath may be pure water or an aqueous solution of iodide (eg, potassium iodide, sodium iodide, etc.). The concentration of the aqueous iodide solution is preferably 0.1-10% by weight. Auxiliaries such as zinc sulfate and zinc chloride may be added to the iodide aqueous solution.

The washing temperature is usually in the range of 5 to 50°C, preferably 10 to 45°C, more preferably 15 to 40°C. The immersion time is usually about 10 to 300 seconds, preferably 20 to 240 seconds. The water washing step may be performed only once, or may be performed multiple times as necessary. When the washing process is carried out multiple times, the types and concentrations of additives contained in the washing bath used for each treatment are appropriately adjusted.

The drying process of the polyvinyl alcohol-based film is performed by any appropriate method (for example, natural drying, air drying, heat drying). The thickness of the polarizer after drying is preferably 3 to 20 μm.

In the present invention, the obtained polarizer may be subjected to surface modification treatment. Examples of the surface modification treatment include corona treatment, plasma treatment, itro treatment, and the like, and corona treatment is particularly preferred. By performing corona treatment, reactive functional groups such as carbonyl groups and amino groups are generated on the surface of the polarizer, and adhesion to the durability-improving layer is improved. In addition, foreign matter on the surface is removed by the ashing effect, and unevenness on the surface is reduced, so that a polarizing film with excellent appearance characteristics can be produced.

In the present invention, the polarizing film includes a polarizer and an adhesive layer adjacent to the polarizer or an optical film other than the polarizer. The polarizing film 10 shown in FIG. 1 includes an adhesive layer adjacent to the optical film (retardation film) 4 other than the polarizer 1 . Moreover, the polarizing film 10 shown in FIG. 2 includes an adhesive layer 5 adjacent to the polarizer 1 . The adhesive layer will be described below.

<Adhesive layer>
The adhesive layer is formed by a cured product layer of an adhesive composition, and in particular, a cured product layer of an active energy ray-curable adhesive composition such as electron beam-curable, ultraviolet-curable, or visible light-curable. It is preferably formed by The thickness of the adhesive layer after drying is preferably 0.01 μm to 5 μm, more preferably 0.01 μm to 3 μm, from the viewpoint of improving the appearance characteristics of the polarizing film. Active energy ray-curable adhesive compositions can be classified into radical polymerization-curable adhesive compositions and cationic polymerizable adhesive compositions. In the present invention, active energy rays with a wavelength range of 10 nm to less than 380 nm are expressed as ultraviolet rays, and active energy rays with a wavelength range of 380 nm to 800 nm are expressed as visible rays.

A radically polymerizable compound is mentioned as a monomer component which comprises a radically polymerizable adhesive composition. Examples of radically polymerizable compounds include compounds having radically polymerizable functional groups of carbon-carbon double bonds such as (meth)acryloyl groups and vinyl groups. These monomer components can be either monofunctional radically polymerizable compounds or multifunctional radically polymerizable compounds having two or more polymerizable functional groups. Moreover, these radical polymerizable compounds can be used individually by 1 type or in combination of 2 or more types. As these radically polymerizable compounds, for example, compounds having a (meth)acryloyl group are suitable. In the present invention, (meth)acryloyl means an acryloyl group and/or a methacryloyl group, and "(meth)" has the same meaning below.

Examples of monofunctional radically polymerizable compounds include (meth)acrylamide derivatives having a (meth)acrylamide group. A (meth)acrylamide derivative is preferable in terms of ensuring adhesiveness to a polarizer and various transparent protective films, and in terms of high polymerization rate and excellent productivity. Specific examples of (meth)acrylamide derivatives include N-methyl(meth)acrylamide, N,N-dimethyl(meth)acrylamide, N,N-diethyl(meth)acrylamide, N-isopropyl(meth)acrylamide, N - N-alkyl group-containing (meth)acrylamide derivatives such as butyl (meth)acrylamide and N-hexyl (meth)acrylamide; N-methylol (meth)acrylamide, N-hydroxyethyl (meth)acrylamide, N-methylol-N- N-hydroxyalkyl group-containing (meth)acrylamide derivatives such as propane (meth)acrylamide; N-aminoalkyl group-containing (meth)acrylamide derivatives such as aminomethyl (meth)acrylamide and aminoethyl (meth)acrylamide; N-methoxymethyl N-alkoxy group-containing (meth)acrylamide derivatives such as acrylamide and N-ethoxymethylacrylamide; N-mercaptoalkyl group-containing (meth)acrylamide derivatives such as mercaptomethyl (meth)acrylamide and mercaptoethyl (meth)acrylamide; be done. Further, the heterocycle-containing (meth)acrylamide derivative in which the nitrogen atom of the (meth)acrylamide group forms a heterocycle includes, for example, N-acryloylmorpholine, N-acryloylpiperidine, N-methacryloylpiperidine, N-acryloylpyrrolidine etc.

Among the (meth)acrylamide derivatives, N-hydroxyalkyl group-containing (meth)acrylamide derivatives are preferred from the viewpoint of adhesion to polarizers and various transparent protective films. , for example, various (meth)acrylic acid derivatives having a (meth)acryloyloxy group. Specifically, for example, methyl (meth) acrylate, ethyl (meth) acrylate, n-propyl (meth) acrylate, isopropyl (meth) acrylate, 2-methyl-2-nitropropyl (meth) acrylate, n-butyl ( meth) acrylate, isobutyl (meth) acrylate, s-butyl (meth) acrylate, t-butyl (meth) acrylate, n-pentyl (meth) acrylate, t-pentyl (meth) acrylate, 3-pentyl (meth) acrylate, 2,2-dimethylbutyl (meth)acrylate, n-hexyl (meth)acrylate, cetyl (meth)acrylate, n-octyl (meth)acrylate, 2-ethylhexyl (meth)acrylate, 4-methyl-2-propylpentyl ( Examples include (meth)acrylic acid (C1-20) alkyl esters such as meth)acrylate and n-octadecyl (meth)acrylate.

Examples of the (meth)acrylic acid derivative include cycloalkyl (meth)acrylates such as cyclohexyl (meth)acrylate and cyclopentyl (meth)acrylate; aralkyl (meth)acrylates such as benzyl (meth)acrylate; (meth) acrylate, 2-norbornylmethyl (meth) acrylate, 5-norbornen-2-yl-methyl (meth) acrylate, 3-methyl-2-norbornylmethyl (meth) acrylate, dicyclopentenyl (meth) ) Polycyclic (meth)acrylates such as acrylate, dicyclopentenyloxyethyl (meth)acrylate, dicyclopentanyl (meth)acrylate; 2-methoxyethyl (meth)acrylate, 2-ethoxy Ethyl (meth) acrylate, 2-methoxymethoxyethyl (meth) acrylate, 3-methoxybutyl (meth) acrylate, ethyl carbitol (meth) acrylate, phenoxyethyl (meth) acrylate, alkylphenoxy polyethylene glycol (meth) acrylate, etc. alkoxy group- or phenoxy group-containing (meth)acrylates; and the like.

Further, the (meth)acrylic acid derivatives include 2-hydroxyethyl (meth)acrylate, 2-hydroxypropyl (meth)acrylate, 3-hydroxypropyl (meth)acrylate, 2-hydroxybutyl (meth)acrylate, 4- Hydroxyalkyl (meth)acrylates such as hydroxybutyl (meth)acrylate, 6-hydroxyhexyl (meth)acrylate, 8-hydroxyoctyl (meth)acrylate, 10-hydroxydecyl (meth)acrylate, and 12-hydroxylauryl (meth)acrylate and hydroxyl group-containing (meth) acrylates such as [4-(hydroxymethyl) cyclohexyl] methyl acrylate, cyclohexanedimethanol mono (meth) acrylate, 2-hydroxy-3-phenoxypropyl (meth) acrylate; glycidyl (meth) acrylate, Epoxy group-containing (meth)acrylates such as 4-hydroxybutyl (meth)acrylate glycidyl ether; 2,2,2-trifluoroethyl (meth)acrylate, 2,2,2-trifluoroethylethyl (meth)acrylate, tetra Halogen-containing (meth)acrylate such as fluoropropyl (meth)acrylate, hexafluoropropyl (meth)acrylate, octafluoropentyl (meth)acrylate, heptadecafluorodecyl (meth)acrylate, 3-chloro-2-hydroxypropyl (meth)acrylate, etc. ) acrylates; alkylaminoalkyl (meth)acrylates such as dimethylaminoethyl (meth)acrylate; 3-oxetanylmethyl (meth)acrylate, 3-methyl-oxetanylmethyl (meth)acrylate, 3-ethyl-oxetanylmethyl (meth)acrylate , 3-butyl-oxetanylmethyl (meth)acrylate, 3-hexyl-oxetanylmethyl (meth)acrylate and other oxetane group-containing (meth)acrylates; tetrahydrofurfuryl (meth)acrylate, butyrolactone (meth)acrylate, and other heterocycles (Meth) acrylate, neopentyl glycol hydroxypivalate (meth) acrylic acid adduct, p-phenylphenol (meth) acrylate, and the like.

Examples of monofunctional radically polymerizable compounds include carboxyl group-containing monomers such as (meth)acrylic acid, carboxyethyl acrylate, carboxypentyl acrylate, itaconic acid, maleic acid, fumaric acid, crotonic acid and isocrotonic acid.

Examples of monofunctional radically polymerizable compounds include lactam vinyl monomers such as N-vinylpyrrolidone, N-vinyl-ε-caprolactam and methylvinylpyrrolidone; vinylpyridine, vinylpiperidone, vinylpyrimidine, vinylpiperazine, vinylpyrazine, Vinyl-based monomers having a nitrogen-containing heterocyclic ring such as vinylpyrrole, vinylimidazole, vinyloxazole, and vinylmorpholine are included.

Moreover, a radically polymerizable compound having an active methylene group can be used as the monofunctional radically polymerizable compound. A radically polymerizable compound having an active methylene group is a compound having an active double bond group such as a (meth)acrylic group at the end or in the molecule and an active methylene group. Active methylene groups include, for example, an acetoacetyl group, an alkoxymalonyl group, a cyanoacetyl group, and the like. Preferably, the active methylene group is an acetoacetyl group. Specific examples of radically polymerizable compounds having an active methylene group include 2-acetoacetoxyethyl (meth)acrylate, 2-acetoacetoxypropyl (meth)acrylate, 2-acetoacetoxy-1-methylethyl (meth)acrylate, and the like. 2-ethoxymalonyloxyethyl (meth)acrylate, 2-cyanoacetoxyethyl (meth)acrylate, N-(2-cyanoacetoxyethyl)acrylamide, N-(2-propionylacetoxybutyl) acrylamide, N-(4-acetoacetoxymethylbenzyl)acrylamide, N-(2-acetoacetylaminoethyl)acrylamide and the like. The radically polymerizable compound having an active methylene group is preferably acetoacetoxyalkyl (meth)acrylate.

Examples of polyfunctional radically polymerizable compounds having two or more polymerizable functional groups include tripropylene glycol di(meth)acrylate, tetraethylene glycol di(meth)acrylate, and 1,6-hexanediol di(meth)acrylate. , 1,9-nonanediol di(meth)acrylate, 1,10-decanediol diacrylate, 2-ethyl-2-butylpropanediol di(meth)acrylate, bisphenol A di(meth)acrylate, bisphenol A ethylene oxide addition di(meth)acrylate, bisphenol A propylene oxide adduct di(meth)acrylate, bisphenol A diglycidyl ether di(meth)acrylate, neopentyl glycol di(meth)acrylate, tricyclodecanedimethanol di(meth) Acrylates, cyclic trimethylolpropane formal (meth)acrylate, dioxane glycol di(meth)acrylate, trimethylolpropane tri(meth)acrylate, pentaerythritol tri(meth)acrylate, pentaerythritol tetra(meth)acrylate, dipentaerythritol penta (Meth)acrylates, dipentaerythritol hexa(meth)acrylate, esters of (meth)acrylic acid and polyhydric alcohols such as EO-modified diglycerol tetra(meth)acrylate, 9,9-bis[4-(2- (Meth)acryloyloxyethoxy)phenyl]fluorene. Specific examples include Aronix M-220 (manufactured by Toagosei Co., Ltd.), light acrylate 1,9ND-A (manufactured by Kyoeisha Chemical Co., Ltd.), light acrylate DGE-4A (manufactured by Kyoeisha Chemical Co., Ltd.), light acrylate DCP-A (Kyoeisha Chemical Co., Ltd.) (manufactured by Sartomer), SR-531 (manufactured by Sartomer), CD-536 (manufactured by Sartomer) and the like. Various epoxy (meth)acrylates, urethane (meth)acrylates, polyester (meth)acrylates, various (meth)acrylate monomers, and the like can also be used as necessary.

In the present invention, the polarizing film comprises a polarizer and an adhesive layer adjacent to the polarizer or an optical film other than the polarizer, and the adhesive layer is formed of a cured product layer of an adhesive composition. Yes, when the cured product obtained by curing the adhesive composition is immersed in pure water at 23 ° C. for 24 hours,
Formula: {(M2−M1)/M1}×100 (%),
However, M1: weight of cured product before immersion, M2: weight of cured product after immersion,
is less than 10% by weight. According to such a configuration, even if a specific metal component contained in the polarizer is mixed into the adhesive layer from the end portion, the bond between the ionized oxalic acid and the metal component, and furthermore, the end portion of the polarizing film movement of oxalate into the interior is inhibited. As a result, the appearance characteristics of the polarizing film are particularly improved even after the humidification durability test. More preferably, the bulk water absorption is less than 8 wt%, particularly preferably less than 6 wt%.

In the present invention, the polarizing film includes a polarizer and an adhesive layer adjacent to the polarizer or an optical film other than the polarizer, and based on the element ratio measurement of the adhesive layer, (number of carbon atoms) / (oxygen The number of atoms+the number of nitrogen atoms) is preferably 2.5 or more. In general, it is believed that the binding of ionized oxalic acid to the metal component and the migration of oxalate occurs through water. Here, when the adhesive layer has a ratio of (the number of carbon atoms)/(the number of oxygen atoms + the number of nitrogen atoms) of 2.5 or more based on the element ratio measurement of the adhesive layer, the adhesive layer is bonded from the end. It suppresses the intrusion of water into the adhesive layer, especially at the edges of the adhesive layer, and prevents the bonding of ionized oxalic acid and metal components, and the movement of oxalate from the edges of the polarizing film to the inside. can be suppressed. As a result, the appearance characteristics of the polarizing film are remarkably improved even after the humidification durability test. A method for measuring the element ratio of the adhesive layer will be described later.

Further, in the present invention, the polarizing film comprises a polarizer and an adhesive layer adjacent to the polarizer or an optical film other than the polarizer, and the adhesive layer is formed of a cured product layer of an adhesive composition. It is preferable that the logPow, which represents the octanol/water partition coefficient based on the weighted average of the molar fractions of the monomer components contained in the adhesive composition, is 1.6 or more. In general, it is believed that the binding of ionized oxalic acid to the metal component and the migration of oxalate occurs through water. Here, when the weighted average of the mole fractions of the monomer components contained in the adhesive composition, logPow representing the octanol/water partition coefficient is 1.6 or more, water from the end into the adhesive layer can be suppressed, especially at the edges of the adhesive layer, bonding between ionized oxalic acid and metal components, and movement of oxalate from the edges of the polarizing film to the inside can be suppressed. As a result, the appearance characteristics of the polarizing film are remarkably improved even after the humidification durability test.

The octanol/water partition coefficient (logPow) is an index representing the lipophilicity of a substance, and means the logarithm of the octanol/water partition coefficient. High logPow means lipophilicity, ie low water absorption. Although the logPow value can be measured (flask immersion method described in JIS-Z-7260), it can also be calculated by calculation. In this specification, logPow values calculated with ChemDraw Ultra manufactured by Cambridge Soft are used.

The log Pow of major radically polymerizable compounds is shown below. Hydroxyethylacrylamide (trade name "HEAA", manufactured by Kojin Co., Ltd., LogPow; -0.56), diethylacrylamide (trade name "DEAA", manufactured by KJ Chemicals, LogPow; 1.69), unsaturated fatty acid hydroxyalkyl ester Modified ε-caprolactone (trade name “PLAXEL FA1DDM”, manufactured by Daicel Corporation, LogPow; 1.06), N-vinylformamide (trade name “Beamset 770”, manufactured by Arakawa Chemical Co., LogPow; −0.25), acryloyl Morpholine (trade name “ACMO”, manufactured by KOHJIN Co., Ltd., LogPow; −0.20), γ-butyrolactone acrylate (trade name “GBLA”, manufactured by Osaka Organic Chemical Industry Co., Ltd., LogPow; 0.19), 2 amounts of acrylic acid body (trade name “β-CEA”, manufactured by Daicel Corporation, LogPow; 0.2), N-vinylpyrrolidone (trade name “NVP”, manufactured by Nippon Shokubai Co., Ltd., LogPow; 0.24), acetoacetoxyethyl methacrylate (trade name Name "AAEM", manufactured by Nippon Synthetic Chemical Co., Ltd., LogPow; 0.27), 2-hydroxyethyl acrylate (trade name "HEA", manufactured by Osaka Organic Chemical Industry Co., Ltd., LogPow; 0.28), glycidyl methacrylate (trade name " Light Ester G”, manufactured by Kyoeisha Chemical Co., Ltd., LogPow; 0.57), dimethylacrylamide (trade name “DMAA”, manufactured by Kojin Co., Ltd., LogPow; 0.58), tetrahydrofurfuryl alcohol acrylic acid multimer ester (trade name “ Viscoat #150D", manufactured by Osaka Organic Chemical Industry Co., Ltd., LogPow; 0.60), 4-hydroxybutyl acrylate (trade name "4-HBA", manufactured by Osaka Organic Chemical Industry Co., Ltd., LogPow; 0.68), acrylic acid ( Trade name "acrylic acid", manufactured by Mitsubishi Chemical Corporation, LogPow; 0.69), triethylene glycol diacrylate (trade name "Light Acrylate 3EG-A", manufactured by Kyoeisha Chemical Co., Ltd., LogPow; 0.72), PEG400 # Diacrylate Acrylate (trade name “Light Acrylate 9EG-A”, manufactured by Kyoeisha Chemical Co., Ltd., LogPow; −0.1), polypropylene glycol diacrylate (trade name “Aronix M-220”, manufactured by Toagosei Co., Ltd., LogPow; 1.68) , dicyclopentenyl acrylate (trade name "Funkryl FA-511AS", manufactured by Hitachi Chemical Co., Ltd., LogPow; 2.26), butyl acrylate (trade name "butyl acrylate", manufactured by Mitsubishi Chemical Corporation, LogPow; 2.35), 1,6-hex Sundiol diacrylate (trade name “Light Acrylate 1.6HX-A”, manufactured by Kyoeisha Chemical Co., Ltd., LogPow; 2.43), dicyclopentanyl acrylate (trade name “Funkryl FA-513AS”, Hitachi Chemical company, LogPow; 2.58), dimethylol-tricyclodecane diacrylate (trade name “Light acrylate DCP-A”, Kyoeisha Chemical Co., Ltd., LogPow; 3.05), isobornyl acrylate (trade name “Light acrylate IB-XA", manufactured by Kyoeisha Chemical Co., Ltd., LogPow; 3.27), neopentyl glycol hydroxypivalate acrylic acid adduct (trade name "Light Acrylate HPP-A" manufactured by Kyoeisha Chemical Co., Ltd., LogPow; 3.35), 1,9-nonanediol diacrylate (trade name “Light Acrylate 1,9ND-A”, manufactured by Kyoeisha Chemical Co., Ltd., LogPow; 3.68), o-phenylphenol EO-modified acrylate (trade name “Funkryl FA-301A” , Hitachi Chemical Co., Ltd., LogPow; 3.98), 2-ethylhexyloxetane (trade name "Aron oxetane OXT-212", Toagosei Co., Ltd., LogPow; 4.24), bisphenol-A-diglycidyl ether (trade name "JER828", manufactured by Mitsubishi Chemical Corporation, LogPow; 4.76), bisphenol A EO 6 mol modified diacrylate (trade name "FA-326A", manufactured by Hitachi Chemical Co., LogPow; 4.84), bisphenol A EO 4 mol modified diacrylate Acrylate (trade name "FA-324A", manufactured by Hitachi Chemical Co., Ltd., LogPow; 5.15), bisphenol A PO 2 molar modified diacrylate (trade name "FA-P320A", manufactured by Hitachi Chemical Co., Ltd., LogPow; 6.10), Bisphenol A PO3 molar modified diacrylate (trade name "FA-P323A", manufactured by Hitachi Chemical Co., Ltd., LogPow; 6.26), bisphenol A PO4 molar modified diacrylate (trade name "FA-P324A", manufactured by Hitachi Chemical Co., Ltd., LogPow ; 6.43), lauryl acrylate (trade name “Light Acrylate LA”, manufactured by Kyoeisha Chemical Co., Ltd., LogPow; 6), isostearyl acrylate (trade name “ISTA”), manufactured by Osaka Organic Chemical Industry Co., Ltd.; LogPow; 7 .46) and the like.

The adhesive layer is formed of a cured product layer of an adhesive composition, and log Pow represents the octanol/water partition coefficient by the weighted average of the mole fractions of the monomer components contained in the adhesive composition. is 1.6 or more, it is preferable to contain 25 parts by weight or more of a monomer component having an alkyl group having 8 or more carbon atoms per 100 parts by weight of the total amount of the monomer components. Examples of the monomer component having an alkyl group having 8 or more carbon atoms include the aforementioned dicyclopentanyl acrylate (trade name “Funkryl FA-513AS” manufactured by Hitachi Chemical Co., Ltd., LogPow; 2.58), Lauryl acrylate (trade name “Light Acrylate LA”, manufactured by Kyoeisha Chemical Co., Ltd., LogPow; 6), isostearyl acrylate (trade name “ISTA”), manufactured by Osaka Organic Chemical Industry; LogPow; 7.46), etc. be done.

The adhesive layer is formed of a cured product layer of an adhesive composition, and log Pow represents the octanol/water partition coefficient by the weighted average of the mole fractions of the monomer components contained in the adhesive composition. is 1.6 or more, the content of the monomer component having a hydroxyl group is preferably 40 parts by weight or less. In addition, as the monomer component having a hydroxyl group, the monomer component having a hydroxyl group among the aforementioned monomer components can be mentioned.

Further, in the present invention, the polarizing film comprises a polarizer and an adhesive layer adjacent to the polarizer or an optical film other than the polarizer, and the adhesive layer is formed of a cured product layer of an adhesive composition. When the total amount of the monomer components is 100 parts by weight, the adhesive composition preferably contains 25 parts by weight or more of a monomer component having two or more polymerizable functional groups, and preferably 30 parts by weight. It is more preferable to contain at least Even if oxalate is generated in such an adhesive layer, the high hardness of the adhesive layer inhibits crystal growth of oxalate. As a result, the generation of foreign substances caused by oxalate is suppressed, and the appearance characteristics of the polarizing film are significantly improved.

Examples of the monomer component having two or more polymerizable functional groups include the aforementioned multifunctional radically polymerizable compounds having two or more polymerizable functional groups. In particular, when the adhesive composition contains 25 parts by weight or more of a monomer component having two or more polymerizable functional groups when the total amount of the monomer components is 100 parts by weight, the monomer having a hydroxyl group It is preferable to set the content of the component to 40 parts by weight or less.

In the present invention, the adhesive composition, which is a raw material for the adhesive layer of the polarizing film, may contain an acrylic oligomer obtained by polymerizing a (meth)acrylic monomer in addition to the radically polymerizable compound. By containing an acrylic oligomer in the adhesive composition, curing shrinkage when the composition is irradiated with an active energy ray and cured is reduced, and the adhesive layer and the adherend such as a polarizer and an optical film It is possible to reduce the interfacial stress with As a result, deterioration in adhesion between the adhesive layer and the adherend can be suppressed.

Considering the workability and uniformity during coating, the active energy ray-curable adhesive preferably has a low viscosity, so the acrylic oligomer obtained by polymerizing the (meth)acrylic monomer also has a low viscosity. is preferred. The acrylic oligomer which has a low viscosity and can prevent curing shrinkage of the adhesive layer preferably has a weight-average molecular weight (Mw) of 15,000 or less, more preferably 10,000 or less, and particularly 5,000 or less. preferable. On the other hand, in order to sufficiently suppress curing shrinkage of the cured product layer (adhesive layer), the weight average molecular weight (Mw) of the acrylic oligomer is preferably 500 or more, more preferably 1000 or more. 1500 or more is particularly preferable. Specific examples of the (meth)acrylic monomer constituting the acrylic oligomer include methyl (meth)acrylate, ethyl (meth)acrylate, n-propyl (meth)acrylate, isopropyl (meth)acrylate, 2-methyl- 2-nitropropyl (meth)acrylate, n-butyl (meth)acrylate, isobutyl (meth)acrylate, S-butyl (meth)acrylate, t-butyl (meth)acrylate, n-pentyl (meth)acrylate, t-pentyl (meth) acrylate, 3-pentyl (meth) acrylate, 2,2-dimethylbutyl (meth) acrylate, n-hexyl (meth) acrylate, cetyl (meth) acrylate, n-octyl (meth) acrylate, 2-ethylhexyl ( (Meth)acrylic acid (C1-20) alkyl esters such as meth)acrylate, 4-methyl-2-propylpentyl (meth)acrylate, N-octadecyl (meth)acrylate, and further, for example, cycloalkyl (meth) ) acrylates (e.g., cyclohexyl (meth) acrylate, cyclopentyl (meth) acrylate, etc.), aralkyl (meth) acrylates (e.g., benzyl (meth) acrylate, etc.), polycyclic (meth) acrylates (e.g., 2-isobornyl (meth) ) acrylate, 2-norbornylmethyl (meth)acrylate, 5-norbornen-2-yl-methyl (meth)acrylate, 3-methyl-2-norbornylmethyl (meth)acrylate, etc.), hydroxyl group-containing (meth) ) Acrylic esters (e.g., hydroxyethyl (meth)acrylate, 2-hydroxypropyl (meth)acrylate, 2,3-dihydroxypropylmethyl-butyl (meth)methacrylate, etc.), alkoxy group- or phenoxy group-containing (meth)acryl Acid esters (2-methoxyethyl (meth)acrylate, 2-ethoxyethyl (meth)acrylate, 2-methoxymethoxyethyl (meth)acrylate, 3-methoxybutyl (meth)acrylate, ethyl carbitol (meth)acrylate, phenoxy ethyl (meth)acrylate, etc.), epoxy group-containing (meth)acrylic acid esters (e.g., glycidyl (meth)acrylate, etc.), halogen-containing (meth)acrylic acid esters (e.g., 2,2,2-trifluoroethyl (meth)acrylate, 2,2,2- trifluoroethylethyl (meth)acrylate, tetrafluoropropyl (meth)acrylate, hexafluoropropyl (meth)acrylate, octafluoropentyl (meth)acrylate, heptadecafluorodecyl (meth)acrylate, etc.), alkylaminoalkyl (meth)acrylate acrylates (eg, dimethylaminoethyl (meth)acrylate, etc.), and the like. These (meth)acrylates can be used alone or in combination of two or more. Specific examples of the acrylic oligomer (E) include "ARUFON" manufactured by Toagosei Co., Ltd., "ACT FLOW" manufactured by Soken Chemical Co., Ltd., and "JONCRYL" manufactured by BASF Japan.

The amount of the acrylic oligomer compounded is usually preferably 15 parts by weight or less with respect to 100 parts by weight of the total amount of the monomer components in the adhesive composition. If the content of the acrylic oligomer in the composition is too high, the reaction rate when the composition is irradiated with an active energy ray will decrease significantly, resulting in poor curing in some cases. On the other hand, in order to sufficiently suppress curing shrinkage of the adhesive layer, the composition preferably contains 3 parts by weight or more of the acrylic oligomer.

A photopolymerization initiator in the case of using a radically polymerizable compound is appropriately selected depending on the active energy ray. When curing with ultraviolet light or visible light, a photopolymerization initiator that is cleaved with ultraviolet light or visible light is used. Examples of the photopolymerization initiator include benzophenone compounds such as benzyl, benzophenone, benzoylbenzoic acid, and 3,3′-dimethyl-4-methoxybenzophenone; 4-(2-hydroxyethoxy)phenyl(2-hydroxy-2 -propyl)ketone, α-hydroxy-α,α'-dimethylacetophenone, 2-methyl-2-hydroxypropiophenone, α-hydroxycyclohexylphenylketone and other aromatic ketone compounds; methoxyacetophenone, 2,2-dimethoxy- Acetophenone compounds such as 2-phenylacetophenone, 2,2-diethoxyacetophenone, 2-methyl-1-[4-(methylthio)-phenyl]-2-morpholinopropane-1; benzoin methyl ether, Benzoin ether compounds such as benzoin ethyl ether, benzoin isopropyl ether, benzoin butyl ether, and anisoin methyl ether; aromatic ketal compounds such as benzyl dimethyl ketal; aromatic sulfonyl chlorides such as 2-naphthalenesulfonyl chloride photoactive oxime compounds such as 1-phenone-1,1-propanedione-2-(o-ethoxycarbonyl)oxime; thioxanthone, 2-chlorothioxanthone, 2-methylthioxanthone, 2,4-dimethylthioxanthone, thioxanthone compounds such as isopropylthioxanthone, 2,4-dichlorothioxanthone, 2,4-diethylthioxanthone, 2,4-diisopropylthioxanthone, dodecylthioxanthone; camphorquinone; halogenated ketones; can give.

The blending amount of the photopolymerization initiator is 20% by weight or less when the total amount of the active energy ray-curable adhesive composition is 100% by weight. The blending amount of the photopolymerization initiator is preferably 0.01 to 20% by weight, more preferably 0.05 to 10% by weight, further preferably 0.1 to 5% by weight.

When the curable adhesive for a polarizing film of the present invention is used as a visible light-curable adhesive containing a radically polymerizable compound as a curable component, a photopolymerization initiator that is particularly sensitive to light of 380 nm or more is added. It is preferable to use A photopolymerization initiator highly sensitive to light of 380 nm or more will be described later.

As the photopolymerization initiator, a compound represented by the following general formula (1);

（式中、Ｒ^１およびＲ^２は－Ｈ、－ＣＨ_２ＣＨ_３、－ｉＰｒまたはＣｌを示し、Ｒ^１およびＲ^２は同一または異なっても良い）を単独で使用するか、あるいは一般式（１）で表される化合物と後述する３８０ｎｍ以上の光に対して高感度な光重合開始剤とを併用することが好ましい。一般式（１）で表される化合物を使用した場合、３８０ｎｍ以上の光に対して高感度な光重合開始剤を単独で使用した場合に比べて接着性に優れる。一般式（１）で表される化合物の中でも、Ｒ^１およびＲ^２が－ＣＨ_２ＣＨ_３であるジエチルチオキサントンが特に好ましい。接着剤組成物中の一般式（１）で表される化合物の組成比率は、硬化性成分の全量１００重量部に対して、０．１～５重量部であることが好ましく、０．５～４重量部であることがより好ましく、０．９～３重量部であることがさらに好ましい。

(wherein R ¹ and R ² represent —H, —CH ₂ CH ₃ , —iPr or Cl, and R ¹ and R ² may be the same or different), or the general formula ( It is preferable to use the compound represented by 1) together with a photopolymerization initiator highly sensitive to light of 380 nm or longer, which will be described later. When the compound represented by the general formula (1) is used, the adhesiveness is superior to that when a photopolymerization initiator highly sensitive to light of 380 nm or more is used alone. Among the compounds represented by general formula (1), diethylthioxanthone in which R ¹ and R ² are —CH ₂ CH ₃ is particularly preferred. The composition ratio of the compound represented by formula (1) in the adhesive composition is preferably 0.1 to 5 parts by weight, preferably 0.5 to 5 parts by weight, per 100 parts by weight of the total amount of the curable components. It is more preferably 4 parts by weight, and even more preferably 0.9 to 3 parts by weight.

Moreover, it is preferable to add a polymerization initiation aid as necessary. Examples of polymerization initiation aids include triethylamine, diethylamine, N-methyldiethanolamine, ethanolamine, 4-dimethylaminobenzoic acid, methyl 4-dimethylaminobenzoate, ethyl 4-dimethylaminobenzoate, and isoamyl 4-dimethylaminobenzoate. and ethyl 4-dimethylaminobenzoate is particularly preferred. When a polymerization initiation aid is used, the amount added is usually 0 to 5 parts by weight, preferably 0 to 4 parts by weight, most preferably 0 to 3 parts by weight, per 100 parts by weight of the total amount of the curable components. be.

Moreover, a well-known photoinitiator can be used together as needed. Since the transparent protective film having UV absorbability does not transmit light of 380 nm or less, it is preferable to use a photopolymerization initiator that is highly sensitive to light of 380 nm or more. Specifically, 2-methyl-1-(4-methylthiophenyl)-2-morpholinopropan-1-one, 2-benzyl-2-dimethylamino-1-(4-morpholinophenyl)-butanone-1 , 2-(dimethylamino)-2-[(4-methylphenyl)methyl]-1-[4-(4-morpholinyl)phenyl]-1-butanone, 2,4,6-trimethylbenzoyl-diphenyl-phosphine oxide, bis(2,4,6-trimethylbenzoyl)-phenylphosphine oxide, bis(η5-2,4-cyclopentadien-1-yl)-bis(2,6-difluoro-3-(1H-pyrrole- 1-yl)-phenyl) titanium and the like.

In particular, as a photopolymerization initiator, in addition to the photopolymerization initiator of general formula (1), a compound represented by the following general formula (2);

（式中、Ｒ^３、Ｒ^４およびＲ^５は－Ｈ、－ＣＨ_３、－ＣＨ_２ＣＨ_３、－ｉＰｒまたはＣｌを示し、Ｒ^３、Ｒ^４およびＲ^５は同一または異なっても良い）を使用することが好ましい。一般式（２）で表される化合物としては、市販品でもある２－メチル－１－（４－メチルチオフェニル）－２－モルフォリノプロパン－１－オン（商品名：ＩＲＧＡＣＵＲＥ９０７ メーカー：ＢＡＳＦ）が好適に使用可能である。その他、２－ベンジル－２－ジメチルアミノ－１－（４－モルフォリノフェニル）－ブタノン－１（商品名：ＩＲＧＡＣＵＲＥ３６９ メーカー：ＢＡＳＦ）、２－（ジメチルアミノ）－２－［（４－メチルフェニル）メチル］－１－［４－（４－モルホリニル）フェニル］－１－ブタノン（商品名：ＩＲＧＡＣＵＲＥ３７９ メーカー：ＢＡＳＦ）が感度が高いため好ましい。

(wherein R ³ , R ⁴ and R ⁵ represent —H, —CH ₃ , —CH ₂ CH ₃ , —iPr or Cl, and R ³ , R ⁴ and R ⁵ may be the same or different) It is preferred to use As the compound represented by the general formula (2), 2-methyl-1-(4-methylthiophenyl)-2-morpholinopropan-1-one (trade name: IRGACURE907, manufacturer: BASF), which is also a commercial product, is suitable. can be used for Other, 2-benzyl-2-dimethylamino-1-(4-morpholinophenyl)-butanone-1 (trade name: IRGACURE369 manufacturer: BASF), 2-(dimethylamino)-2-[(4-methylphenyl) Methyl]-1-[4-(4-morpholinyl)phenyl]-1-butanone (trade name: IRGACURE379, manufacturer: BASF) is preferred because of its high sensitivity.

In the present invention, it is preferable to use a hydroxyl group-containing photopolymerization initiator among the above photopolymerization initiators. When the active energy ray-curable adhesive composition contains a hydroxyl group-containing photopolymerization initiator as a polymerization initiator, the solubility in the adhesive layer having a high concentration of component A on the polarizer side increases, and the adhesive layer increases the curability of Examples of photopolymerization initiators having a hydroxyl group include 2-methyl-2-hydroxypropiophenone (trade name “DAROCUR1173”, manufactured by BASF), 1-hydroxycyclohexylphenyl ketone (trade name “IRGACURE184”, manufactured by BASF). ), 1-[4-(2-hydroxyethoxy)-phenyl]-2-hydroxy-2-methyl-1-propan-1-one (trade name “IRGACURE2959”, manufactured by BASF), 2-hydroxy-1- {4-[4-(2-Hydroxy-2-methyl-propionyl)-benzyl]phenyl}-2-methyl-propan-1-one (trade name “IRGACURE 127”, manufactured by BASF) and the like. In particular, 1-hydroxycyclohexylphenyl ketone is more preferable because it has particularly excellent solubility in an adhesive layer having a high component A concentration.

The cationically polymerizable compounds used in the cationically polymerizable adhesive composition include monofunctional cationically polymerizable compounds having one cationically polymerizable functional group in the molecule and two or more cationically polymerizable functional groups in the molecule. It is classified into polyfunctional cationic polymerizable compounds with Since the monofunctional cationically polymerizable compound has a relatively low liquid viscosity, the liquid viscosity of the resin composition can be lowered by including it in the resin composition. In addition, the monofunctional cationically polymerizable compound often has a functional group that exhibits various functions, and by including it in the cationically polymerizable adhesive composition, the cationically polymerizable adhesive composition and/or the cationically polymerizable compound Various functions can be expressed in the cured product of the adhesive composition. The polyfunctional cationically polymerizable compound is preferably contained in the cationically polymerizable adhesive composition because the cured product of the cationically polymerizable adhesive composition can be three-dimensionally crosslinked. The ratio of the monofunctional cationically polymerizable compound and the polyfunctional cationically polymerizable compound is such that 100 parts by weight of the monofunctional cationically polymerizable compound is mixed with 10 parts by weight to 1000 parts by weight of the polyfunctional cationically polymerizable compound. is preferred. Examples of cationic polymerizable functional groups include epoxy groups, oxetanyl groups, and vinyl ether groups. Compounds having an epoxy group include aliphatic epoxy compounds, alicyclic epoxy compounds, and aromatic epoxy compounds. It is particularly preferred to contain an alicyclic epoxy compound. Alicyclic epoxy compounds include 3,4-epoxycyclohexylmethyl-3,4-epoxycyclohexanecarboxylate, caprolactone-modified products of 3,4-epoxycyclohexylmethyl-3,4-epoxycyclohexanecarboxylate, and trimethylcaprolactone-modified products. and valerolactone modified products, and specifically, Celoxide 2021, Celoxide 2021A, Celoxide 2021P, Celoxide 2081, Celoxide 2083, Celoxide 2085 (manufactured by Daicel Chemical Industries, Ltd., Cyracure UVR-6105, Cyracure UVR -6107, Cyracure 30, R-6110 (manufactured by Dow Chemical Japan Co., Ltd.), etc. Compounds having an oxetanyl group improve the curability of the cationic polymerizable adhesive composition, Compounds having an oxetanyl group include 3-ethyl-3-hydroxymethyloxetane, 1,4-bis[(3-ethyl-3-oxetanyl ) methoxymethyl]benzene, 3-ethyl-3-(phenoxymethyl)oxetane, di[(3-ethyl-3-oxetanyl)methyl]ether, 3-ethyl-3-(2-ethylhexyloxymethyl)oxetane, phenol Aron oxetane OXT-101, Aron oxetane OXT-121, Aron oxetane OXT-211, Aron oxetane OXT-221, Aron oxetane OXT-212 (manufactured by Toagosei Co., Ltd.) and the like are commercially available. A compound having a vinyl ether group has the effect of improving the curability of the cationic polymerizable adhesive composition and lowering the liquid viscosity of the composition, and is therefore preferably contained. , 2-hydroxyethyl vinyl ether, diethylene glycol monovinyl ether, 4-hydroxybutyl vinyl ether, diethylene glycol monovinyl ether, triethylene glycol divinyl ether, cyclohexanedimethanol divinyl ether, cyclohexanedimethanol monovinyl ether, tricyclodecane vinyl ether, cyclohexyl vinyl ether, methoxyethyl vinyl ether , ethoxyethyl vinyl ether, pentaerythritol type tetravinyl ether, and the like.

The cationically polymerizable adhesive composition contains at least one compound selected from the epoxy group-containing compound, the oxetanyl group-containing compound, and the vinyl ether group-containing compound described above as a curable component, and any of these compounds can be subjected to cationic polymerization. A photo cationic polymerization initiator is blended because it is cured by This cationic photopolymerization initiator generates cationic species or Lewis acid upon irradiation with active energy rays such as visible light, ultraviolet rays, X-rays and electron beams, and initiates the polymerization reaction of epoxy groups and oxetanyl groups. As the photocationic polymerization initiator, a photoacid generator described later is preferably used. Further, when the cationic polymerizable adhesive composition is used with visible light curing, it is preferable to use a cationic photopolymerization initiator that is particularly sensitive to light of 380 nm or more. Since it is a compound that exhibits maximum absorption in a wavelength region near or shorter than 300 nm, by blending a photosensitizer that exhibits maximum absorption in a wavelength region longer than that, specifically, light with a wavelength longer than 380 nm, this It can respond to light of a wavelength in the vicinity and promote the generation of cationic species or acid from the photocationic polymerization initiator. Examples of photosensitizers include anthracene compounds, pyrene compounds, carbonyl compounds, organic sulfur compounds, persulfides, redox compounds, azo and diazo compounds, halogen compounds, photoreducible dyes, and the like. You may use it in mixture of 2 or more types. Anthracene compounds are particularly preferable because of their excellent photosensitizing effect, and specific examples thereof include Anthracure UVS-1331 and Anthracure UVS-1221 (manufactured by Kawasaki Kasei Co., Ltd.). The content of the photosensitizer is preferably 0.1 wt % to 5 wt %, more preferably 0.5 wt % to 3 wt %.

<Optical film>
In the present invention, the optical film included in the polarizing film includes, for example, a transparent protective film and a retardation film. In addition to the polarizer, the optical film may also be subjected to the surface modification treatment. Examples of the surface modification treatment include corona treatment, plasma treatment, itro treatment, and the like, and corona treatment is particularly preferred.

As a material for forming the transparent protective film, thermoplastic resins are used which are excellent in transparency, mechanical strength, thermal stability, water barrier properties, isotropy, and the like. Specific examples of such thermoplastic resins include cellulose resins such as triacetyl cellulose, polyester resins, polyethersulfone resins, polysulfone resins, polycarbonate resins, polyamide resins, polyimide resins, polyolefin resins, (meth)acrylic resins, cyclic Polyolefin resins (norbornene-based resins), polyarylate resins, polystyrene resins, polyvinyl alcohol resins, and mixtures thereof. One or more of any suitable additives may be contained in the transparent protective film. Examples of additives include ultraviolet absorbers, antioxidants, lubricants, plasticizers, release agents, anti-coloring agents, flame retardants, nucleating agents, antistatic agents, pigments, and colorants. The content of the thermoplastic resin in the transparent protective film is preferably 50 to 100% by weight, more preferably 50 to 99% by weight, still more preferably 60 to 98% by weight, and particularly preferably 70 to 97% by weight. . If the content of the thermoplastic resin in the transparent protective film is 50% by weight or less, the high transparency inherent in the thermoplastic resin may not be sufficiently exhibited.

As the material for forming the transparent protective film, a material having excellent transparency, mechanical strength, thermal stability, moisture barrier properties, isotropy, etc. is preferable, and in particular, a material having a moisture permeability of 150 g/m ² /24h or less. is more preferred, 140 g/m ² /24h or less is particularly preferred, and 120 g/m ² /24h or less is even more preferred.

A functional layer such as a hard coat layer, an antireflection layer, an antisticking layer, a diffusion layer or an antiglare layer can be provided on the surface of the transparent protective film to which the polarizer is not adhered. Functional layers such as the hard coat layer, antireflection layer, anti-sticking layer, diffusion layer, and antiglare layer can be provided on the transparent protective film itself, or can be provided separately from the transparent protective film. can also

The thickness of the transparent protective film can be determined as appropriate, but is generally about 1 to 500 μm, preferably 1 to 300 μm, more preferably 5 to 200 μm, from the viewpoint of strength, workability such as handleability, and thinness. preferable. Further, it is preferably 10 to 200 μm, more preferably 20 to 80 μm.

As the transparent protective film, a retardation film having a front retardation of 40 nm or more and/or a thickness direction retardation of 80 nm or more can be used. The front retardation is usually controlled in the range of 40-200 nm, and the thickness direction retardation is usually controlled in the range of 80-300 nm. When a retardation film is used as the transparent protective film, the thickness can be reduced because the retardation film also functions as a transparent protective film.

Examples of the retardation film include a birefringent film obtained by uniaxially or biaxially stretching a polymer material, an oriented film of a liquid crystal polymer, and a film in which an oriented layer of a liquid crystal polymer is supported. Although the thickness of the retardation film is not particularly limited, it is generally about 20 to 150 μm.

As the retardation film, the following formulas (1) to (3):
0.70<Re[450]/Re[550]<0.97 (1)
1.5×10−3<Δn<6×10−3 (2)
1.13<NZ<1.50 (3)
(Wherein, Re [450] and Re [550] are the in-plane retardation values of the retardation film measured with light having wavelengths of 450 nm and 550 nm, respectively, at 23 ° C., and Δn is the slow phase of the retardation film In-plane birefringence that is nx-ny when the refractive indices in the axial direction and the fast axis direction are nx and ny, respectively, and NZ is the refractive index in the thickness direction of the retardation film, (ratio of nx-nz, which is birefringence in the thickness direction, to nx-ny, which is in-plane birefringence) may be used.

The polarizing film according to the present invention can be produced, for example, by the following production method.
A method for producing a polarizing film comprising a polarizer and an adhesive layer adjacent to a first optical film other than the polarizer, wherein the polarizer and the first optical film are bonded together via a water-based adhesive layer. A method for producing a polarizing film, comprising: a first bonding step of bonding; and a second bonding step of bonding the first optical film and the second optical film via the adhesive layer. The polarizer preferably contains a metal component capable of becoming a divalent metal cation in water, particularly zinc. Moreover, it is preferable that the adhesive layer is formed of a cured product layer of an active energy ray-curable adhesive composition.

Moreover, the polarizing film according to the present invention can also be produced, for example, by the following production method.
A method for producing a polarizing film comprising a polarizer and an adhesive layer adjacent to the polarizer, comprising: a first bonding step of bonding the polarizer and a first optical film via the adhesive layer; A manufacturing method of a polarizing film provided. The polarizer preferably contains a metal component capable of becoming a divalent metal cation in water, particularly zinc. Moreover, it is preferable that the adhesive layer is formed of a cured product layer of an active energy ray-curable adhesive composition.

In the adhesion step, various adhesive compositions are applied to adherends such as polarizers and optical films, the adherends such as polarizers and optical films are bonded together, and the adhesive compositions are cured. The method of applying the adhesive composition is appropriately selected depending on the viscosity of the adhesive composition and the desired thickness. A die coater, a bar coater, a rod coater and the like can be mentioned. Bonding of adherends such as polarizers and optical films can be carried out using a roll laminator or the like.

The adhesive layer is formed of a cured product layer of an adhesive composition, and in particular, a cured product of an active energy ray-curable adhesive composition such as electron beam-curable, ultraviolet-curable, or visible light-curable. It is preferably formed by layers. In the bonding step, an active energy ray (electron beam, ultraviolet light, visible light, etc.) is applied to cure the adhesive composition to form an adhesive layer. The irradiation direction of the active energy rays (electron beam, ultraviolet rays, visible rays, etc.) can be any suitable direction. When the polarizing film according to the present invention is produced in a continuous line, the line speed is preferably 5 to 100 m/min, more preferably 10 to 50 m/min, and even more preferably 20 to 20, depending on the curing time of the adhesive composition. 30 m/min. If the line speed is too low, the productivity is poor, or the damage to the transparent protective film is too great, and a polarizing film that can withstand a durability test or the like cannot be produced. If the line speed is too high, the curing of the curable resin composition may be insufficient, and the intended adhesiveness may not be obtained.

The polarizing film of the present invention can be used as an optical film laminated with other optical layers in practical use. The optical layer is not particularly limited. One or more optical layers may be used. In particular, a reflective polarizing film or a semi-transmissive polarizing film obtained by further laminating a reflector or a semi-transmitting reflector on the polarizing film of the present invention, an elliptical polarizing film or circularly polarized light obtained by further laminating a retardation plate on the polarizing film A film, a wide viewing angle polarizing film obtained by further laminating a viewing angle compensation film on a polarizing film, or a polarizing film obtained by further laminating a brightness enhancement film on a polarizing film are preferable.

An optical film obtained by laminating the above optical layer on a polarizing film can be formed by a method of sequentially and separately laminating in the manufacturing process of a liquid crystal display device or the like. It has the advantage of improving the manufacturing process of liquid crystal display devices due to its excellent stability and assembly work. Appropriate adhesive means such as an adhesive layer can be used for lamination. When the above polarizing film and other optical films are adhered, their optical axes can be arranged at an appropriate angle according to the desired retardation characteristics.

The polarizing film and the optical film having at least one layer of polarizing film laminated thereon may be provided with an adhesive layer for adhering to other members such as a liquid crystal cell. The pressure-sensitive adhesive that forms the pressure-sensitive adhesive layer is not particularly limited, but for example, an acrylic polymer, silicone-based polymer, polyester, polyurethane, polyamide, polyether, fluorine-based polymer, rubber-based polymer, or the like is appropriately selected. can be used as In particular, those having excellent optical transparency, suitable wettability, cohesiveness, and adhesive properties such as acrylic pressure-sensitive adhesives, and excellent weather resistance and heat resistance can be preferably used.

The adhesive layer can also be provided on one side or both sides of the polarizing film or the optical film as a superimposed layer of different compositions or types. Further, when the adhesive layer is provided on both sides, the front and back surfaces of the polarizing film or the optical film may have adhesive layers with different compositions, types, thicknesses, and the like. The thickness of the adhesive layer can be appropriately determined according to the purpose of use, adhesive strength, etc., and is generally 1 to 100 μm, preferably 5 to 30 μm, particularly preferably 10 to 20 μm.

The exposed surface of the adhesive layer is temporarily covered by a separator for the purpose of preventing contamination, etc., until the adhesive layer is put into practical use. This prevents contact with the adhesive layer during normal handling conditions. As the separator, excluding the above thickness conditions, suitable thin sheets such as plastic films, rubber sheets, paper, cloth, non-woven fabrics, nets, foam sheets, metal foils, and laminates thereof may be used. An appropriate release agent according to the prior art, such as one coated with an appropriate release agent such as chain alkyl, fluorine, or molybdenum sulfide, can be used.

The polarizing film or optical film of the present invention can be preferably used for forming various devices such as liquid crystal display devices. Formation of the liquid crystal display device can be carried out according to the conventional method. That is, a liquid crystal display device is generally formed by appropriately assembling components such as a liquid crystal cell, a polarizing film or an optical film, and, if necessary, an illumination system, and incorporating a driving circuit. There is no particular limitation except that the polarizing film or optical film according to the invention is used, and conventional methods can be applied. As for the liquid crystal cell, any type such as TN type, STN type, or π type can be used.

Appropriate liquid crystal displays can be formed, such as a liquid crystal display having a polarizing film or an optical film arranged on one or both sides of a liquid crystal cell, or a liquid crystal display using a backlight or a reflector for an illumination system. In that case, the polarizing film or optical film according to the present invention can be placed on one side or both sides of the liquid crystal cell. When polarizing films or optical films are provided on both sides, they may be the same or different. Furthermore, when forming a liquid crystal display device, for example, appropriate parts such as a diffuser plate, an anti-glare layer, an antireflection film, a protective plate, a prism array, a lens array sheet, a light diffuser plate, and a backlight are arranged in a single layer or at an appropriate position. Two or more layers can be arranged.

Examples of the present invention are described below, but embodiments of the present invention are not limited to these.

<Production of polarizer>
A polyvinyl alcohol film having an average degree of polymerization of 2700 and a thickness of 45 μm was stretched and transported while being dyed between rolls having different peripheral speed ratios. First, while swelling the polyvinyl alcohol film by immersing it in a water bath at 30° C. for 1 minute, it was stretched 1.2 times in the conveying direction (first stretching), then potassium iodide (0.03% by weight) and iodine. (0.3% by weight) in an aqueous solution (liquid temperature 30° C.) for 1 minute, and then stretched 3 times (based on the unstretched film) in the conveying direction while being dyed (second stretching). Next, this stretched film was immersed in an aqueous solution (bath solution) of boric acid (4% by weight), potassium iodide (5% by weight) and zinc sulfate (3.5% by weight) for 30 seconds while The film was stretched 6 times (based on the unstretched film) (third stretching). Polarizer 1 was obtained by drying this stretched film. The thickness of the polarizer 1 after drying was 18 μm. Further, a polarizer 2 was obtained by the same manufacturing method as the polarizer 1 except that a polyvinyl alcohol film having a thickness of 30 μm was used. The thickness of the polarizer 2 after drying was 12 μm.

<Active energy ray>
Visible light (gallium-encapsulated metal halide lamp) as the active energy ray Irradiation device: Light HAMMER10 manufactured by Fusion UV Systems, Inc. Bulb: V bulb Peak illuminance: 1600 mW/cm ² , integrated irradiation amount 1000/mJ/cm ² (wavelength 380- 440 nm) was used. The illuminance of visible light was measured using a Sola-Check system manufactured by Solatell.

<Method for Measuring Element Ratio of Adhesive Layer>
The element ratio of the adhesive layer provided in the polarizing film was measured by the following measuring method.
First, for both the polarizing film configuration (1) and the polarizing film configuration (2) below, an adhesive that does not constitute a polarizing film was applied to the surface of the second optical film and fixed to a metal support. Next, the adhesive and the first optical film or the second optical film were removed with an ultramicrotome to expose the adhesive layer to be measured. Next, Ar-GCIB etching treatment was performed, and the adhesive layer exposed after the Ar-GCIB etching treatment was pressed and fixed to the sample table with a Mo plate. Thereafter, ESCA analysis was performed using a scanning X-ray photoelectron spectrometer (Quantum 2000 manufactured by ULVAC-PHI), wide scan measurement was performed, and qualitative analysis was performed. Further, narrow scan measurement was performed for carbon element, oxygen element and nitrogen element, and the element ratio (atomic %) was calculated. From the obtained carbon element ratio (atomic%), oxygen element ratio (atomic%), and nitrogen element ratio (atomic%), (number of carbon atoms)/(number of oxygen atoms + number of nitrogen atoms) was calculated. .

<Panel lighting test>
An in-vehicle on-dash monitor (TKH703) manufactured by MAXWIN was disassembled and the liquid crystal panel was taken out. The polarizing film attached to the viewing side of the liquid crystal panel is peeled off, and instead, the polarizing film according to each of the manufactured examples and comparative examples is cut to the same size as the polarizing film peeled off from the liquid crystal panel, and the adhesive A layer (thickness: 20 μm) was interposed between the polarizing film and the peeled off polarizing film, and the liquid crystal panel was obtained by adhering such that the transmission axis was the same.

The liquid crystal panel obtained above was placed in an environment of 65° C. and 95% for 1000 hours, and then left in an environment of normal temperature and normal humidity for 24 hours. After that, the liquid crystal panel was remounted in the disassembled monitor housing, and a black image was displayed for visual confirmation. As a result, ◯ was given when only a black screen was displayed, and x was given when a white haze-like display defect occurred on a part of the screen.

<Third optical film>
The third optical film used in the following polarizing film configuration (1) was produced by the following production method.

An autoclave equipped with a stirrer, cooling tube, nitrogen inlet tube and thermometer was charged with 48 parts by weight of hydroxypropyl methylcellulose (manufactured by Shin-Etsu Chemical Co., Ltd., trade name Metolose 60SH-50), 15601 parts by weight of distilled water, 8161 parts by weight of diisopropyl fumarate, and acrylic. 240 parts by weight of 3-ethyl-3-oxetanylmethyl acid and 45 parts by weight of t-butyl peroxypivalate, which is a polymerization initiator, are added, nitrogen bubbling is performed for 1 hour, and the mixture is maintained at 49° C. for 24 hours while stirring. Thus, radical suspension polymerization was carried out. It was then cooled to room temperature and the suspension containing the polymer particles formed was centrifuged. The resulting polymer was washed twice with distilled water and twice with methanol, and then dried under reduced pressure.

The obtained fumaric acid ester resin (polymer having negative birefringence) was dissolved in a toluene/methyl ethyl ketone mixed solution (toluene/methyl ethyl ketone 50% by weight/50% by weight) to obtain a 20% solution. Further, 5 parts by weight of tributyl trimellitate as a plasticizer was added to 100 parts by weight of the fumaric acid ester resin to prepare a dope.

As the support film, a biaxially stretched polyester (polyethylene-terephthalate/isophthalate copolymer) film (thickness: 75 μm, width: 1350 mm) was used. The tensile modulus (MD) of the support at 140°C was 800 MPa.

The roll of the support film was set in the feeding section of the film forming apparatus, the support film was fed out, and was heat-treated in a heating furnace while being transported downstream. The temperature of the heat treatment was adjusted by changing the atmospheric temperature in the heating furnace. The heating time was adjusted by changing the transport speed of the support. The dope prepared in Synthesis Example A was coated on the heat-treated support so that the film thickness after drying was 6.3 μm, and dried at 140°C. The dried coating film was wound up as a laminate together with the support.

The above-mentioned laminate was set in the feeding section of a stretching device, and free-end uniaxial stretching was performed in a stretching furnace at a temperature of 140° C. while feeding the laminate and conveying it to the downstream side. The support was peeled off from the stretched laminate to obtain a retardation film having a thickness of 6 μm. The draw ratio was adjusted so that the in-plane retardation of the retardation film after peeling the support was 35 nm.

Example 1
As an adhesive, an aqueous solution containing a polyvinyl alcohol resin containing acetoacetyl groups (average degree of polymerization: 1200, degree of saponification: 98.5 mol%, degree of acetoacetylation: 5 mol%) and methylolmelamine at a weight ratio of 3:1. was used. Using this adhesive, a second optical film (a triacetyl cellulose film with a hard coat layer (manufactured by Fuji Film Co., Ltd., product name “TG40UL”, film thickness 40 μm)), and a first optical film (retardation-containing cycloolefin film (manufactured by Nippon Zeon Co., Ltd., product name “ZT12”, film 17 μm thick))) were bonded together by a roll bonding machine, and subsequently heat-dried in an oven to produce a laminated film in which optical films were laminated on both sides of a polarizer.

Next, an MCD coater (manufactured by Fuji Machine Co., Ltd.) (cell shape: honeycomb, number of gravure roll lines: 1000 / inch, rotation speed: 140% / pair) was applied to the cycloolefin film side with retardation of the laminated film obtained above. Using the line speed), the adhesive composition adjusted to the formulation amount shown in Table 1 was coated so as to have a thickness of 1 μm, and was laminated to the third optical film (thickness 6 μm))) with a roll machine. . After that, from the third optical film side, the above visible light was irradiated from the active energy ray irradiation device to cure the adhesive composition, and then dried with hot air at 70° C. for 3 minutes to obtain a polarizing film (of this configuration). The polarizing film is referred to as "polarizing film configuration (1)"). The thickness of the adhesive layer after drying was 1 μm. The lamination line speed was 25 m/min.

A sample for humidification durability test evaluation was prepared by bonding the polarizing film according to Example 1 produced in Example 1 to one side of 0.7 mm thick alkali-free glass via an adhesive layer (thickness: 20 μm). A humidity durability test was carried out by exposing the sample to an environment of 65° C.-95% humidity for 1000 hours. Regarding the sample for evaluating the humidification durability test after the humidification durability test, a pressure-sensitive adhesive layer (thickness: 20 μm) was formed on the other side of the non-alkaline glass polarizing film laminated with the polarizing film according to Example 1. After pasting the crossed Nicol polarizing film so that the transmission axes of the respective polarizing films are perpendicular to each other, it is placed on the backlight (the polarizing film according to Example 1 is the upper surface), and the polarizing film according to Example 1 is The polarizing film was visually observed to evaluate the presence or absence of bright spots originating from foreign matter.

After a humidification durability test in which the film was exposed to an environment of 65° C. and 95% humidity for 1000 hours, the polarizing film according to Example 1 did not have bright spots derived from foreign matter beyond 3 mm from the end surface. .

Example 4
As an adhesive, an aqueous solution containing a polyvinyl alcohol resin containing acetoacetyl groups (average degree of polymerization: 1200, degree of saponification: 98.5 mol%, degree of acetoacetylation: 5 mol%) and methylolmelamine at a weight ratio of 3:1. was used. Using this adhesive, a second optical film (a triacetyl cellulose film with a hard coat layer (manufactured by Fuji Film Co., Ltd., product name “TG40UL”, film thickness 40 μm))) was laminated with a roll laminator, and then heat-dried in an oven to produce a laminated film in which an optical film was laminated on one side of a polarizer.

Next, on the polarizer 1 side of the laminated film, using an MCD coater (manufactured by Fuji Machinery Co., Ltd.) (cell shape: honeycomb, gravure roll line number: 1000 / inch, rotation speed 140% / relative to line speed), The adhesive composition adjusted to the blending amount shown in Table 1 was coated so as to have a thickness of 1 μm, and the first optical film (cycloolefin film (trade name “ZF14” manufactured by Nippon Zeon Co., Ltd., film thickness 13 μm)) was applied. It was pasted together by a roll machine. After that, from the cycloolefin film side, the visible light was irradiated from the active energy ray irradiation device to cure the adhesive composition, and then dried with hot air at 70 ° C. for 3 minutes to obtain a polarizing film (polarized light with this configuration The film is referred to as "polarizing film configuration (2)"). The thickness of the adhesive layer after drying was 1 μm. The lamination line speed was 25 m/min.

The produced polarizing film according to Example 4 was subjected to a humidification durability test in which it was exposed to an environment of 65 ° C.-95% humidity for 1000 hours in the same manner as in Example 1, and the appearance of bright spots derived from foreign matter was visually observed. was observed.

After a humidification durability test in which the film was exposed to an environment of 65° C. and 95% humidity for 1000 hours, the polarizing film according to Example 2 did not have bright spots originating from foreign matter beyond 3 mm from the end face. .

Examples 3-5, Comparative Examples 1-6
In the same manner as in Examples 1 and 4, except that the configuration of the polarizing film, the formulation of the adhesive composition, and the type of polarizer were changed to those shown in Table 1, the presence or absence of bright spots derived from foreign matter was determined. Observed.

Details of each component listed in Table 1 are as follows.
(Monofunctional radically polymerizable compound)
- Unsaturated fatty acid hydroxyalkyl ester-modified ε-caprolactone (monomer component having a hydroxyl group) (trade name “PLAXEL FA1DDM” manufactured by Daicel, molecular weight 230.26, LogPow; 1.06)
- Acryloylmorpholine (trade name "ACMO", manufactured by Kojin Co., Ltd., molecular weight 141.17, LogPow; -0.20)
- Diethylacrylamide (trade name "DEAA", manufactured by KJ Chemicals, molecular weight 127.18, LogPow; 1.69)
・ Lauryl acrylate (trade name “Light Acrylate LA”, manufactured by Kyoeisha Chemical Co., Ltd., molecular weight 240.39, LogPow; 6)
・Isostearyl acrylate (trade name “ISTA”), manufactured by Osaka Organic Chemical Industry Co., Ltd., molecular weight 324.5, LogPow; 7.46)
- Dicyclopentanyl acrylate (trade name "Funkryl FA-513AS", manufactured by Hitachi Chemical Co., Ltd., molecular weight 206.28, LogPow; 2.58)
(Polyfunctional radically polymerizable compound)
・ PEG400 # diacrylate (trade name “Light Acrylate 9EG-A”, manufactured by Kyoeisha Chemical Co., Ltd., molecular weight 536.61, LogPow; -0.1)
· Polypropylene glycol diacrylate (trade name "Aronix M-220", manufactured by Toagosei Co., Ltd., molecular weight 300.35, LogPow; 1.68)
1,9-nonanediol diacrylate (trade name “Light Acrylate 1,9ND-A”, manufactured by Kyoeisha Chemical Co., Ltd., molecular weight 268.35, LogPow; 3.68)
Dimethylol-tricyclodecane diacrylate (trade name “Light Acrylate DCP-A”, manufactured by Kyoeisha Chemical Co., Ltd., molecular weight 304.38, LogPow; 3.05)
(acrylic oligomer)
· 34/66 molar ratio copolymerized oligomer of butyl acrylate and methacrylate (trade name “ARUFON UP-1190”, manufactured by Toagosei Co., Ltd., molecular weight 1700, LogPow; 1.95)
(initiator)
2-methyl-1-[4-(methylthio)phenyl]-2-morpholinopropan-1-one (trade name "Omnirad 907", manufactured by IGM Resins B.V., molecular weight 279.13, LogPow; 2.09 )
- Diethylthioxanthone (trade name "KAYACURE DETX-S", manufactured by Nippon Kayaku Co., Ltd., molecular weight 268.37, LogPow; 5.12)

In Table 1, "(number of carbon atoms) / (number of oxygen atoms + number of nitrogen atoms)" is calculated based on the above "method for measuring element ratio of adhesive layer", and "average log Pow" is "logPow representing the octanol/water partition coefficient by the weighted average of the molar fractions of the monomer components contained in the adhesive composition" and "the distance from the edge surface to the foreign matter (μm)" , the distance to the bright spot originating from the confirmed foreign matter”, respectively.

REFERENCE SIGNS LIST 10 polarizing film 1 polarizer 2 water-based adhesive 3, 4, 6 optical film 5 adhesive layer 7 adhesive layer

Claims (7)

A polarized light comprising a polarizer and a first optical film laminated on at least one surface of the polarizer with a water-based adhesive layer interposed therebetween, and an adhesive layer on the surface of the first optical film opposite to the water-based adhesive layer. a film,
The polarizer contains zinc ,
The adhesive layer is formed of a cured product layer of an adhesive composition and contains oxalic acid, and the adhesive composition is polymerized when the total amount of the monomer components is 100 parts by weight. containing 25 parts by weight or more of a monomer component having two or more functional groups,
A polarizing film having no bright spots originating from foreign matter beyond 3 mm from an end face after a humidification durability test in which the film is exposed to an environment of 65° C. and 95% humidity for 1000 hours. 2. The polarizing film according to claim 1, wherein the adhesive composition contains 40 parts by weight or less of the monomer component having a hydroxyl group when the total amount of the monomer components is 100 parts by weight. The polarizing film comprises a polarizer and an optical film laminated on at least one surface of the polarizer with a water-based adhesive layer interposed therebetween, and an adhesive layer on the surface of the optical film opposite to the water-based adhesive layer. The polarizing film according to claim 1 or 2 , comprising: 4. The polarizing film according to any one of claims 1 to 3 , wherein the adhesive layer is formed of a cured product layer of an active energy ray-curable adhesive composition. When the adhesive layer is formed of a cured product layer of an adhesive composition, and the cured product obtained by curing the adhesive composition is immersed in pure water at 23 ° C. for 24 hours,
Formula: {(M2−M1)/M1}×100 (%),
However, M1: weight of cured product before immersion, M2: weight of cured product after immersion,
The polarizing film according to any one of claims 1 to 4 , which has a bulk water absorption of less than 10% by weight. 6. An optical film comprising a laminate of at least one polarizing film according to any one of claims 1 to 5 . An image display device comprising the polarizing film according to any one of claims 1 to 5 and/or the optical film according to claim 6 .

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