JP6235370B2 - Production method of polarizing laminated film and polarizing plate - Google Patents

Description

  The present invention relates to a method for producing a polarizing laminate film and a method for producing a polarizing plate. Moreover, this invention relates to the polarizing plate obtained by the said manufacturing method, and a display apparatus provided with the same.

  The polarizing plate has been widely used in display devices such as liquid crystal display devices, particularly in thin televisions and various mobile devices in recent years. As a polarizing plate, the thing of the structure which bonded the protective film which consists of a thermoplastic resin to the single side | surface or both surfaces of a polarizer is common.

  With the widespread use of flat-screen TVs and mobile devices, there is an increasing demand for thinner polarizing plates. As a method for producing a polarizing plate having a thin film polarizer, a method using a base film, also referred to as a “coating method” in the present specification, is known (for example, Patent Documents 1 and 2).

  The coating method is usually a step of forming a resin layer on a base film by coating; a step of drawing and dyeing this resin layer as a polarizer layer to obtain a polarizing laminated film; on the polarizing layer of the polarizing laminated film A step of bonding a protective film to the substrate; and a step of peeling and removing the base film after bonding of the protective film. According to this method, it is possible to easily realize the thinning of the polarizer layer, and hence the polarizing plate, and the thin film polarizer layer and the resin layer serving as a precursor thereof are always supported by the base film or the protective film and are used alone. Since it is not handled by the film, it is excellent in handling of the film during the process.

JP 2011-128486 A JP 2013-186389 A

  The polarizing plate is required to have durability against a heat shock test (cooling shock test) in order to ensure stability against a rapid temperature difference that can be exposed when mounted on a display device or the like. The heat shock test is a test in which an operation of alternately exposing to a high temperature environment (for example, about 70 to 85 ° C.) for a certain time after being exposed to a low temperature environment (for example, about −40 to −30 ° C.) alternately is repeated. is there. The fixed time is usually 30 to 60 minutes, and when “low temperature → high temperature →” is one cycle, it is usually repeated 50 to 400 cycles.

  However, when the heat shock test is performed on the polarizing plate having a protective film on the polarizer layer by the study by the present inventor, the polarizing plate is manufactured using the base film as in the coating method described above. In this case, it has been clarified that a problem that the polarizer layer breaks without being able to withstand expansion and contraction due to a temperature change (hereinafter, this problem is referred to as “warming”) is likely to occur. In particular, this problem of cracking is applied to one or both sides of the polarizer layer when the polarizer layer is thinned in order to meet the demand for thinning the polarizing plate, or to meet the demand for thinning the polarizing plate. This is remarkable when the protective film (in particular, a film having a relatively low rigidity such as a thermoplastic resin film) is thinned and the reinforcing effect of the polarizer layer by the protective film is weakened.

  The object of the present invention is to form a polarizing laminate film by forming a polarizer layer on a substrate film as in the above-mentioned coating method, and further to produce a polarizing plate using this, in a heat shock test. It is providing the method for manufacturing the light-polarizing laminated film which can give the polarizing plate which is hard to produce.

  Another object of the present invention is to provide a method for producing a polarizing plate which hardly causes cracks in a heat shock test. Still another object is to provide a polarizing plate that is resistant to cracking in the heat shock test and has high durability against a rapid temperature difference, and a display device using the same.

  The present invention is based on the following examination results by the present inventor. That is, in a polarizing plate produced by a method in which a polarizer layer is formed on a substrate film to form a polarizing laminate film, and a protective film is bonded onto the polarizer layer, and then the substrate film is peeled and removed. The crack generated in the layer is mainly caused by the minute unevenness on the surface of the polarizer layer exposed by peeling and removing the base film, and this unevenness is the surface state of the base film on the polarizer layer side. I found out that it was influenced.

In other words, in the manufacturing method using the base film, the shape of the surface on the polarizer layer side exposed by peeling and removing the base film is affected by the shape of the surface of the polarizer layer in the base film. This is unavoidable and reflects the surface shape of the base film. The smoothness of the surface on the side of the polarizer layer exposed by peeling and removing the base film reflects the surface shape of the base film. The arithmetic average roughness Ra ₁ exceeds a specific value, or the difference between the arithmetic average roughness Ra ₁ and the arithmetic average roughness Ra ₂ of the polarizer layer surface on which the protective film is bonded is specified. When the value was exceeded, it became clear that cracking was likely to occur in the heat shock test starting from the surface irregularities.

  This invention is made | formed based on the above knowledge, and provides the manufacturing method of the following polarizing laminated film, the manufacturing method of a polarizing plate, a polarizing plate, and a display apparatus.

[1] A step of forming a polyvinyl alcohol resin layer on the base film surface to obtain a laminated film;
Stretching the laminated film to obtain a stretched film;
A step of obtaining a polarizing laminated film by dyeing a polyvinyl alcohol-based resin layer of the stretched film with a dichroic dye to form a polarizer layer;
Including
The polyvinyl alcohol arithmetic average roughness Ra ₀ of the substrate film surface where the resin layer is formed is less than 130 nm, the production method of the polarizing laminate film.

  [2] The manufacturing method according to [1], wherein the polyvinyl alcohol-based resin layer is formed by applying a coating liquid containing a polyvinyl alcohol-based resin.

[3] A step of producing the polarizing laminated film according to [1] or [2];
A step of bonding a first protective film to a surface of the polarizer layer opposite to the base film;
Peeling and removing the base film;
In this order.

[4] The production method according to [3], wherein an arithmetic average roughness Ra ₁ of a surface appearing by peeling and removing the base film in the polarizing plate obtained by peeling and removing the base film is 55 nm or less.

[5] Arithmetic average roughness Ra _{1 of the} surface appearing by peeling and removing the base film in the polarizing plate obtained by peeling and removing the base film, and the base in the polarizer layer constituting the polarizing laminated film The method according to [3] or [4], wherein the difference from the arithmetic average roughness Ra ₂ on the surface opposite to the film is 15 nm or less in absolute value.

  [6] The manufacturing method according to any one of [3] to [5], wherein a thickness of a polarizer layer constituting the polarizing laminated film is 10 μm or less.

  [7] The manufacturing method according to any one of [3] to [6], wherein the first protective film is a thermoplastic resin film.

  [8] The method further includes a step of bonding a second protective film made of a thermoplastic resin to a surface appearing by peeling and removing the base film in the polarizing plate obtained by peeling and removing the base film. [7] The production method according to any one of [7].

[9] A polarizing plate obtained by the production method according to any one of [3] to [8].
[10] The polarizing plate according to [9], comprising an adhesive layer laminated on at least one surface.

  [11] A display device comprising the polarizing plate according to [9] or [10].

  According to the present invention, a polarizing laminated film obtained by a predetermined method is manufactured, and a polarizing plate is manufactured using the same, so that it is difficult to cause cracking in a heat shock test and has high durability against a sudden temperature difference. A board and a display device can be provided.

It is a flowchart which shows the manufacturing method of the light-polarizing laminated film which concerns on this invention, and the manufacturing method of a polarizing plate. It is a schematic sectional drawing which shows an example of the laminated constitution of the laminated | multilayer film obtained at a resin layer formation process. It is a schematic sectional drawing which shows an example of the laminated constitution of the stretched film obtained at a extending process. It is a schematic sectional drawing which shows an example of the laminated constitution of the light-polarizing laminated film obtained at a dyeing process. It is a schematic sectional drawing which shows an example of the laminated constitution of the polarizing laminated film with a protective film obtained at a 1st protective film bonding process. It is a schematic sectional drawing which shows the layer structure of the polarizing plate with a single-sided protective film obtained by a peeling process. It is a schematic sectional drawing which shows the layer structure of the polarizing plate with a double-sided protective film obtained at a 2nd protective film bonding process.

<Method for producing polarizing laminated film>
With reference to FIG. 1, the polarizing laminated film which is a manufacturing intermediate of a polarizing plate has the following processes:
Resin layer forming step S10 for obtaining a laminated film by forming a polyvinyl alcohol-based resin layer on at least one surface of the base film,
Stretching step S20 to stretch the laminated film to obtain a stretched film,
Dyeing step S30 to obtain a polarizing laminated film by dyeing a polyvinyl alcohol resin layer of a stretched film with a dichroic dye to form a polarizer layer,
Manufactured by a method comprising:

  In addition, the light-polarizing laminated film in this invention means a thing provided with the base material film and the polarizer layer laminated | stacked on the at least one surface, and the protective film is not bonded. . In order to distinguish the polarizing laminated film formed by bonding the first protective film to the polarizer layer in the first protective film laminating step S40 from the polarizing laminated film below, “polarizing laminated film with protective film” Also called “film”.

(1) Resin layer forming step S10
With reference to FIG. 2, this step is a step of forming the laminated film 100 by forming the polyvinyl alcohol-based resin layer 6 on at least one surface of the base film 30. The polyvinyl alcohol-based resin layer 6 is a layer that becomes the polarizer layer 5 through the stretching step S20 and the dyeing step S30. The polyvinyl alcohol-based resin layer 6 can be formed by applying a coating liquid containing a polyvinyl alcohol-based resin to one or both surfaces of the base film 30 and drying the coating layer.

  The base film 30 can be composed of a thermoplastic resin, and among them, it is preferably composed of a thermoplastic resin that is excellent in transparency, mechanical strength, thermal stability, stretchability, and the like. Specific examples of such thermoplastic resins include, for example, polyolefin resins such as chain polyolefin resins and cyclic polyolefin resins (norbornene resins, etc.); polyester resins; (meth) acrylic resins; cellulose triacetate, Cellulose ester resins such as cellulose diacetate; Polycarbonate resins; Polyvinyl alcohol resins; Polyvinyl acetate resins; Polyarylate resins; Polystyrene resins; Polyethersulfone resins; Polysulfone resins; Polyamide resins; System resins; and mixtures and copolymers thereof.

  The base film 30 may have a single-layer structure made of one resin layer made of one kind or two or more kinds of thermoplastic resins, or a plurality of resin layers made of one kind or two or more kinds of thermoplastic resins. A laminated multilayer structure may be used. The base film 30 is preferably made of a resin that can be stretched at a stretching temperature suitable for stretching the polyvinyl alcohol-based resin layer 6 when the laminated film 100 is stretched in the stretching step S20 described later.

  The base film 30 can contain an additive. Examples of the additive include an ultraviolet absorber, an antioxidant, a lubricant, a plasticizer, a release agent, an anti-coloring agent, a flame retardant, a nucleating agent, an antistatic agent, a pigment, and a coloring agent. The content of the thermoplastic resin in the base film 30 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. .

  The thickness of the base film 30 is usually 1 to 500 μm, preferably 1 to 300 μm, more preferably 5 to 200 μm, and still more preferably 5 to 150 μm from the viewpoint of workability such as strength and handleability.

In the present invention, the arithmetic average roughness Ra ₀ of the surface of the base film 30 on which the polyvinyl alcohol-based resin layer 6 is formed (which may be one or both surfaces of the base film 30) is 130 nm or less. By adjusting the arithmetic average roughness Ra ₀ within this range, the surface on the polarizer layer side of the polarizing plate obtained by the production method using the polarizing laminated film described later can be smoothed. The cracks of the polarizer layer 5 starting from unevenness can be effectively suppressed. From the viewpoint of more effectively suppressing cracking, the arithmetic average roughness Ra ₀ is preferably 120 nm or less, more preferably 100 nm or less, and even more preferably 80 nm or less.

The arithmetic average roughness Ra ₀ (the same applies to Ra ₁ and Ra ₂ described later) is an index that defines the surface roughness defined in JIS B 0601-2001. According to this, it can be said that a thing with large arithmetic average roughness has many surface irregularities and / or a thing with large. The arithmetic average roughness is usually a statistical value in units of length (mainly nm) since it is calculated by calculating a difference in height from the average height of each raw point. Arithmetic mean roughness can be calculated easily by, for example, obtaining surface images with a confocal microscope such as PLμ2300 sold by Senso Co., Ltd., and then performing statistical processing using the attached software. Can be obtained.

Specific examples of the method for adjusting the arithmetic average roughness Ra ₀ of the base film 30 to 130 nm or less will be described below, but are not limited thereto.

  [A] When the base film 30 is formed by extrusion, the difference between the resin melting temperature at the time of extrusion and the temperature of the chill roll used for cooling the molten film is increased. Increasing the temperature difference increases the amount of temperature change during film cooling and quenching is advantageous for reducing the arithmetic average roughness. The temperature difference can be increased by setting the resin melting temperature as high as possible without causing problems such as deterioration of the resin and excessive decrease in viscosity, and cooling the chill roll as much as possible.

  In particular, when a crystalline thermoplastic resin is used, since crystallization occurs during the cooling process, it is advantageous for reducing the arithmetic average roughness to suppress crystal growth by rapid cooling. Generally, the temperature difference is preferably 100 ° C. or higher, more preferably 240 ° C. or higher, and further preferably higher than 240 ° C., although it depends on the type of thermoplastic resin used. Even in the case of using an amorphous thermoplastic resin, the cooling process of the resin greatly affects the surface irregularities of the base film 30, so that the temperature difference is preferably as large as possible.

  [I] Reduce the amount of nucleating agent and other additives. In the case of using a crystalline thermoplastic resin, in many cases, it is widely known to add a substance called a nucleating agent, which becomes a crystal nucleus for controlling crystal growth. This nucleating agent is suitable for improving the handleability and heat resistance because it imparts rigidity to the base film 30, but if it is added too much, the amount of crystals generated during extrusion becomes very large. Surface irregularities are likely to occur in the material film 30. Therefore, the amount of nucleating agent added is preferably 2% by weight or less (with the thermoplastic resin as 100%). Since other additives such as antioxidants, ultraviolet absorbers, lubricants and matting agents can also affect the surface irregularities, the addition amount is preferably 20% by weight or less.

  [U] Adjust the surface roughness of the chill roll. When the surface roughness of the chill roll is high due to mat treatment or the like, irregularities are likely to occur on the surface of the base film that comes into contact therewith. Therefore, when a chill roll having a low surface roughness is used or a chill roll having a high surface roughness is used, the base film surface opposite to the side in contact with the chill roll is defined as the surface on which the polyvinyl alcohol-based resin layer 6 is formed. It is preferable to do. When forming the polyvinyl alcohol-type resin layer 6 on both surfaces of the base film 30, it is preferable to use a chill roll having a low surface roughness. The arithmetic average roughness of the base film surface opposite to the side contacting the chill roll should be reduced, for example, by adjusting the air volume or the wind speed until the molten resin coming out of the extrusion die contacts the chill roll. Can do.

  [D] When the base film 30 is formed by the casting method, the surface roughness of the support for casting is adjusted. A stainless steel belt or mirror roll can be used as the support, but the higher the surface smoothness, the more advantageous is the reduction of arithmetic mean roughness. The arithmetic average roughness of the base film surface opposite to the side in contact with the support depends greatly on the drying conditions after casting.For example, the solvent evaporation rate can be controlled by selecting the solvent and optimizing the drying equipment. It can be reduced by adjusting.

  Next, the coating liquid applied to the base film 30 will be described. The coating liquid is preferably a polyvinyl alcohol resin solution obtained by dissolving polyvinyl alcohol resin powder in a good solvent (for example, water). Examples of the polyvinyl alcohol resin include polyvinyl alcohol resins and derivatives thereof. Derivatives of polyvinyl alcohol resins include polyvinyl formal, polyvinyl acetal, etc., as well as polyvinyl alcohol resins modified with olefins such as ethylene and propylene; unsaturated carboxylic acids such as acrylic acid, methacrylic acid and crotonic acid. Denatured; modified with alkyl ester of unsaturated carboxylic acid; modified with acrylamide. The proportion of modification is preferably less than 30 mol%, and more preferably less than 10 mol%. When the modification exceeding 30 mol% is performed, it is difficult to adsorb the dichroic dye, which may cause a problem that the polarization performance is lowered. Among the above-mentioned polyvinyl alcohol resins, it is preferable to use a polyvinyl alcohol resin.

  The average degree of polymerization of the polyvinyl alcohol-based resin is preferably in the range of 100 to 10000, more preferably in the range of 1000 to 10000, still more preferably in the range of 1500 to 8000, and in the range of 2000 to 5000. Most preferably. The average degree of polymerization can be determined by a method defined in JIS K 6726-1994 “Testing method for polyvinyl alcohol”. If the average degree of polymerization is less than 100, it is difficult to obtain preferable polarization performance, and if it exceeds 10,000, the solubility in a solvent is deteriorated, and the formation of the polyvinyl alcohol-based resin layer 6 becomes difficult.

  The polyvinyl alcohol resin is preferably a saponified product of a polyvinyl acetate resin. The range of the saponification degree is preferably 80 mol% or more, more preferably 90 mol% or more, and particularly preferably 94 mol% or more. If the degree of saponification is too low, there is a possibility that the water resistance and heat-and-moisture resistance when a polarizing laminate film and further a polarizing plate are not sufficient. Further, it may be a completely saponified product (having a saponification degree of 100 mol%), but if the saponification degree is too high, the dyeing speed becomes slow, and the production time is required to give sufficient polarization performance. In some cases, a polarizer layer having sufficient polarization performance may not be obtained. Therefore, the saponification degree is preferably 99.5 mol% or less, more preferably 99.0 mol% or less.

The degree of saponification is the unit ratio (mol%) of the ratio of acetate groups (acetoxy groups: -OCOCH ₃ ) contained in polyvinyl acetate resin, which is a raw material for polyvinyl alcohol resins, to hydroxyl groups by saponification treatment. The following formula:
Saponification degree (mol%) = [(number of hydroxyl groups) ÷ (number of hydroxyl groups + number of acetate groups)] × 100
Defined by The saponification degree can be determined according to JIS K 6726 (1994). The higher the degree of saponification, the higher the proportion of hydroxyl groups, and thus the lower the proportion of acetate groups that inhibit crystallization.

  Examples of the polyvinyl acetate resin include polyvinyl acetate, which is a homopolymer of vinyl acetate, and copolymers with other monomers copolymerizable with vinyl acetate. Examples of other monomers copolymerizable with vinyl acetate include unsaturated carboxylic acids, olefins, vinyl ethers, unsaturated sulfonic acids, and acrylamides having an ammonium group.

  The coating liquid may contain additives such as a plasticizer and a surfactant as necessary. As the plasticizer, polyol or a condensate thereof can be used, and examples thereof include glycerin, diglycerin, triglycerin, ethylene glycol, propylene glycol, and polyethylene glycol. The blending amount of the additive is preferably 20% by weight or less of the polyvinyl alcohol resin.

  The coating liquid is applied to the base film 30 by a wire bar coating method; a roll coating method such as reverse coating or gravure coating; a die coating method; a comma coating method; a lip coating method; a spin coating method; The method can be appropriately selected from a method such as a fountain coating method, a dipping method, and a spray method.

  The drying temperature and drying time of the coating layer (polyvinyl alcohol-based resin layer before drying) are set according to the type of solvent contained in the coating solution. A drying temperature is 50-200 degreeC, for example, Preferably it is 60-150 degreeC. When the solvent contains water, the drying temperature is preferably 80 ° C. or higher.

  The polyvinyl alcohol-based resin layer 6 may be formed only on one surface of the base film 30 or may be formed on both surfaces. When formed on both sides, two polarizing plates can be obtained from one polarizing laminated film 300, which is advantageous in terms of production efficiency of the polarizing plate.

  The thickness of the polyvinyl alcohol-based resin layer 6 in the laminated film 100 is preferably 3 to 30 μm, and more preferably 5 to 20 μm. If the polyvinyl alcohol-based resin layer 6 has a thickness within this range, the dichroic dye has good dyeability and excellent polarization performance through a stretching step S20 and a dyeing step S30 described later, and is sufficiently thin (for example, A polarizer layer 5 (thickness of 10 μm or less) can be obtained. If the thickness of the polyvinyl alcohol-based resin layer 6 is less than 3 μm, the film becomes too thin after stretching and the dyeability tends to deteriorate.

  Prior to the application of the coating liquid, in order to improve the adhesion between the base film 30 and the polyvinyl alcohol resin layer 6, at least the surface of the base film 30 on the side where the polyvinyl alcohol resin layer 6 is formed is provided. Corona treatment, plasma treatment, flame (flame) treatment or the like may be performed.

  Prior to coating the coating liquid, the polyvinyl alcohol resin layer 6 is provided on the base film 30 via a primer layer or the like in order to improve the adhesion between the base film 30 and the polyvinyl alcohol resin layer 6. May be formed.

  The primer layer can be formed by applying a primer layer forming coating solution to the surface of the substrate film 30 and then drying it. The primer layer forming coating solution contains a component that exhibits a certain degree of strong adhesion to both the base film 30 and the polyvinyl alcohol-based resin layer 6. The primer layer-forming coating solution usually contains a resin component that imparts such adhesion and a solvent. As the resin component, a thermoplastic resin excellent in transparency, thermal stability, stretchability and the like is preferably used, and examples thereof include (meth) acrylic resins and polyvinyl alcohol resins. Among these, polyvinyl alcohol resins that give good adhesion are preferably used. More preferably, it is a polyvinyl alcohol resin. As the solvent, a general organic solvent or an aqueous solvent capable of dissolving the resin component is usually used, but it is preferable to form the primer layer from a coating solution containing water as a solvent.

  In order to increase the strength of the primer layer, a crosslinking agent may be added to the primer layer forming coating solution. A suitable crosslinking agent is appropriately selected from known ones such as organic and inorganic based on the type of thermoplastic resin to be used. Examples of cross-linking agents include epoxy-based, isocyanate-based, dialdehyde-based, metal-based (for example, metal salts, metal oxides, metal hydroxides, organometallic compounds), and polymer-based cross-linking agents. . When a polyvinyl alcohol resin is used as the resin component for forming the primer layer, a polyamide epoxy resin, a methylolated melamine resin, a dialdehyde crosslinking agent, a metal chelate compound crosslinking agent, or the like is preferably used.

  The thickness of the primer layer is preferably about 0.05 to 1 μm, more preferably 0.1 to 0.4 μm. When the thickness is less than 0.05 μm, the effect of improving the adhesion between the base film 30 and the polyvinyl alcohol-based resin layer 6 is small, and when the thickness is more than 1 μm, it is disadvantageous for thinning the polarizing plate.

  The method for applying the primer layer forming coating solution to the base film 30 can be the same as the coating solution for forming the polyvinyl alcohol-based resin layer. The primer layer is applied to the surface on which the coating liquid for forming the polyvinyl alcohol-based resin layer is applied. The drying temperature of the coating layer made of the primer layer forming coating solution is, for example, 50 to 200 ° C, and preferably 60 to 150 ° C. When the solvent contains water, the drying temperature is preferably 80 ° C. or higher.

(2) Stretching step S20
With reference to FIG. 3, this process extends | stretches the laminated | multilayer film 100 which consists of the base film 30 and the polyvinyl alcohol-type resin layer 6, and is extended | stretched which consists of the extended base film 30 'and the polyvinyl alcohol-type resin layer 6'. In this step, the film 200 is obtained. The stretching process is usually uniaxial stretching.

  The stretching ratio of the laminated film 100 can be appropriately selected depending on the desired polarization characteristics, but is preferably more than 5 times and not more than 17 times, more preferably more than 5 times the original length of the laminated film 100. 8 times or less. When the draw ratio is 5 times or less, the polyvinyl alcohol-based resin layer 6 ′ is not sufficiently oriented, and the degree of polarization of the polarizer layer 5 may not be sufficiently high. On the other hand, when the draw ratio exceeds 17 times, the film is likely to be broken during stretching, and the thickness of the stretched film 200 becomes unnecessarily thin, and the workability and handleability in subsequent processes may be reduced.

  The stretching process is not limited to stretching in one stage, and can be performed in multiple stages. In this case, all of the multistage stretching processes may be performed continuously before the dyeing process S30, or the second and subsequent stretching processes may be performed simultaneously with the dyeing process and / or the crosslinking process in the dyeing process S30. Good. Thus, when performing a extending | stretching process in multistage, it is preferable to perform an extending | stretching process so that it may become a draw ratio more than 5 times combining all the stages of an extending | stretching process.

  The stretching treatment may be longitudinal stretching that extends in the film longitudinal direction (film transport direction), and may be lateral stretching or oblique stretching that extends in the film width direction. Examples of the longitudinal stretching method include inter-roll stretching using a roll, compression stretching, stretching using a chuck (clip), and the like, and examples of the lateral stretching method include a tenter method. As the stretching treatment, either a wet stretching method or a dry stretching method can be adopted. However, it is preferable to use the dry stretching method because the stretching temperature can be selected from a wide range.

  The stretching temperature is set to be equal to or higher than the temperature at which the polyvinyl alcohol-based resin layer 6 and the entire base film 30 can be stretched, and preferably the phase transition temperature (melting point or glass transition temperature) of the base film 30. It is in the range of −30 ° C. to + 30 ° C., more preferably in the range of −30 ° C. to + 5 ° C., and still more preferably in the range of −25 ° C. to + 0 ° C. When the base film 30 consists of a plurality of resin layers, the phase transition temperature means the highest phase transition temperature among the phase transition temperatures exhibited by the plurality of resin layers.

  If the stretching temperature is lower than the phase transition temperature of −30 ° C., high-strength stretching exceeding 5 times is difficult to achieve, or the fluidity of the base film 30 is too low and the stretching treatment tends to be difficult. When the stretching temperature exceeds + 30 ° C. of the phase transition temperature, the fluidity of the base film 30 is too large and stretching tends to be difficult. Since it is easier to achieve a high draw ratio of more than 5 times, the drawing temperature is within the above range, and more preferably 120 ° C. or higher.

  As a heating method of the laminated film 100 in the stretching process, a zone heating method (for example, a method in which hot air is blown and heated in a stretching zone such as a heating furnace adjusted to a predetermined temperature); There is a method of heating the roll itself; a heater heating method (a method in which infrared heaters, halogen heaters, panel heaters, etc. are installed above and below the laminated film 100 and heated by radiant heat). In the inter-roll stretching method, the zone heating method is preferable from the viewpoint of the uniformity of the stretching temperature.

  Prior to the stretching step S20, a preheat treatment step for preheating the laminated film 100 may be provided. As the preheating method, the same method as the heating method in the stretching process can be used. The preheating temperature is preferably in the range of −50 ° C. to ± 0 ° C. of the stretching temperature, and more preferably in the range of −40 ° C. to −10 ° C. of the stretching temperature.

  Moreover, you may provide a heat setting process process after the extending | stretching process in extending process S20. The heat setting process is a process in which heat treatment is performed at a temperature equal to or higher than the crystallization temperature while maintaining the tensioned state with the end of the stretched film 200 held by a clip. The crystallization of the polyvinyl alcohol-based resin layer 6 'is promoted by this heat setting treatment. The temperature of the heat setting treatment is preferably in the range of −0 ° C. to −80 ° C. of the stretching temperature, and more preferably in the range of −0 ° C. to −50 ° C. of the stretching temperature.

(3) Dyeing step S30
With reference to FIG. 4, this step is a step in which the polarizer layer 5 is formed by dyeing the polyvinyl alcohol resin layer 6 ′ of the stretched film 200 with a dichroic dye and adsorbing and orienting it. Through this step, a polarizing laminated film 300 in which the polarizer layer 5 is laminated on one side or both sides of the base film 30 ′ is obtained. Specifically, iodine or a dichroic organic dye can be used as the dichroic dye.

  The dyeing step can be performed by immersing the entire stretched film 200 in a solution (dyeing solution) containing a dichroic dye. As the staining solution, a solution in which the above dichroic dye is dissolved in a solvent can be used. As a solvent for the dyeing solution, water is generally used, but an organic solvent compatible with water may be further added. The concentration of the dichroic dye in the dyeing solution is preferably 0.01 to 10% by weight, more preferably 0.02 to 7% by weight, and further preferably 0.025 to 5% by weight. preferable.

  When iodine is used as the dichroic dye, it is preferable to further add iodide to the dyeing solution containing iodine because the dyeing efficiency can be further improved. Examples of iodide include potassium iodide, lithium iodide, sodium iodide, zinc iodide, aluminum iodide, lead iodide, copper iodide, barium iodide, calcium iodide, tin iodide, and titanium iodide. Is mentioned. The iodide concentration in the dyeing solution is preferably 0.01 to 20% by weight. Of the iodides, it is preferable to add potassium iodide. When potassium iodide is added, the ratio of iodine to potassium iodide is preferably in the range of 1: 5 to 1: 100, more preferably in the range of 1: 6 to 1:80, by weight. Preferably, it is in the range of 1: 7 to 1:70. The temperature of the dyeing solution is preferably in the range of 10-60 ° C, more preferably in the range of 20-40 ° C.

  In addition, although it is possible to perform dyeing process S30 before extending process S20, or to perform these processes simultaneously, the dichroic dye adsorb | sucked to a polyvinyl alcohol-type resin layer can be orientated favorably. As described above, it is preferable that the dyeing step S30 is performed after the laminated film 100 is subjected to at least some stretching treatment. That is, the stretched film 200 obtained by subjecting the stretching process to the target magnification in the stretching process S20 can be used for the dyeing process S30, and after performing the stretching process at a lower ratio than the target in the stretching process S20. In the dyeing step S30, the stretching process can be performed until the total stretching ratio reaches the target ratio. As the latter embodiment, 1) an embodiment in which, after the stretching process is performed at a lower ratio than the target in the stretching process S20, the stretching process is performed so that the total stretching ratio becomes the target ratio during the dyeing process in the dyeing process S30. As will be described later, when the crosslinking treatment is performed after the dyeing treatment, 2) after the stretching treatment is performed at a lower magnification than the target in the stretching step S20, the total stretching ratio is the target during the dyeing treatment in the dyeing step S30. Examples include a mode in which the stretching process is performed to such an extent that the ratio does not reach the ratio, and then the stretching process is performed during the crosslinking process so that the final total stretching ratio becomes a target ratio.

  The dyeing step S30 may include a crosslinking treatment step that is performed subsequent to the dyeing treatment. The crosslinking treatment can be performed by immersing the dyed film in a solution containing a crosslinking agent (crosslinking solution). As the crosslinking agent, conventionally known substances can be used, and examples thereof include boron compounds such as boric acid and borax, glyoxal, and glutaraldehyde. A crosslinking agent may be used individually by 1 type, and may use 2 or more types together.

  Specifically, the crosslinking solution can be a solution in which a crosslinking agent is dissolved in a solvent. As the solvent, for example, water can be used, but an organic solvent compatible with water may be further included. The concentration of the crosslinking agent in the crosslinking solution is preferably in the range of 1 to 20% by weight, and more preferably in the range of 6 to 15% by weight.

  The cross-linking solution can contain iodide. By adding iodide, the polarization performance in the plane of the polarizer layer 5 can be made more uniform. Examples of iodide include potassium iodide, lithium iodide, sodium iodide, zinc iodide, aluminum iodide, lead iodide, copper iodide, barium iodide, calcium iodide, tin iodide, and titanium iodide. Is mentioned. The concentration of iodide in the crosslinking solution is preferably 0.05 to 15% by weight, and more preferably 0.5 to 8% by weight. The temperature of the crosslinking solution is preferably in the range of 10 to 90 ° C.

  The crosslinking treatment can be performed simultaneously with the dyeing treatment by blending a crosslinking agent in the dyeing solution. Further, a stretching process may be performed during the crosslinking process. The specific mode for carrying out the stretching treatment during the crosslinking treatment is as described above. Moreover, you may perform the process immersed in a crosslinking solution 2 or more times using 2 or more types of crosslinking solutions from which a composition differs.

  It is preferable to perform a washing | cleaning process and a drying process after dyeing process S30 and before 1st protective film bonding process S40 mentioned later. The washing process usually includes a water washing process. The water washing treatment can be performed by immersing the film after the dyeing treatment or after the crosslinking treatment in pure water such as ion exchange water or distilled water. The water washing temperature is usually in the range of 3 to 50 ° C, preferably 4 to 20 ° C. The washing step may be a combination of a water washing step and a washing step with an iodide solution.

  As a drying process performed after the washing process, any appropriate method such as natural drying, blow drying, and heat drying can be adopted. For example, in the case of heat drying, the drying temperature is usually 20 to 95 ° C.

  The thickness of the polarizer layer 5 included in the polarizing laminated film 300 can be, for example, 30 μm or less, and further 20 μm or less, but is preferably 10 μm or less from the viewpoint of thinning the polarizing plate, and is 8 μm or less. Is more preferable. The thickness of the polarizer layer 5 is usually 2 μm or more.

The arithmetic average roughness Ra ₂ of the surface opposite to the base film 30 ′ in the polarizer layer 5 of the polarizing laminated film 300 is applied to the base film 30 with a coating liquid containing a polyvinyl alcohol resin. When the polarizer layer 5 is formed through the stretching and dyeing steps, it is usually 55 nm or less, and more typically about 40 nm or less.

<Production method of polarizing plate>
With reference to FIG. 1, the manufacturing method of the polarizing plate according to the present invention includes the following steps:
1st protective film bonding process S40 which bonds a 1st protective film to the surface on the opposite side to the base film in the polarizer layer of the polarizing laminated film manufactured by the above-mentioned method,
Peeling process S50 for peeling and removing the base film,
Are included in this order.

  The polarizing plate with a single-sided protective film in which the first protective film is bonded to one surface of the polarizer layer is obtained through the first protective film bonding step S40 and the peeling step S50. Moreover, as shown in FIG. 1, after the peeling step S50, the second protective film is formed on a surface (hereinafter, this surface is also referred to as “peeled surface”) that appears by peeling and removing the base film in the polarizing plate with a single-side protective film. The 2nd protective film bonding process S60 which bonds may be provided, and a polarizing plate with a double-sided protective film may be obtained.

According to the above manufacturing method, a polarizing plate (polarized light with a single-sided or double-sided protective film) is formed using a polarizing laminated film in which a polarizer layer is formed on a surface having an arithmetic average roughness Ra ₀ of 130 nm or less. Plate), it is difficult to cause cracks in the heat shock test, and a polarizing plate having high durability against a rapid temperature difference can be obtained.

  Here, the cracking effect of the polarizer layer and the cracking suppression effect according to the present invention will be described in more detail. When cold heat is repeated in the heat shock test, each layer of the polarizing plate made of a plastic polymer repeatedly expands and contracts due to thermal expansion. Furthermore, if the protective film has distortion during molding, or if the polymer constituting it is oriented, relaxation behavior is also added, so the film dimensions change gradually with each cycle. Go (usually shrinks). Also in the polarizer layer, in addition to expansion and contraction due to thermal expansion, forces such as contraction due to orientation relaxation and cross-linking contraction due to boric acid act and try to contract considerably strongly.

  In the heat shock test, the polarizing plate is very high every time the cycle is repeated due to the contraction force of the polarizer layer to contract and the distortion caused by the complicated movement of the layers arranged around it. Internal stress is generated. The crack of the polarizer layer is a problem that the polarizer layer is broken along the orientation direction of the polyvinyl alcohol resin highly oriented by the internal stress.

  As described above, the cause of cracking is assumed to be a protective film and a glass substrate on which a polarizing plate is bonded during testing (a display cell such as a practical liquid crystal cell). )) (In other words, the properties of these peripheral members), but in order to actually crack, the internal stress caused by these factors often concentrates specifically. The present inventor has found that a defect site that becomes a starting point of cracks needs to be present in the polarizing plate, and that the surface unevenness of the release surface of the polarizing plate can form the defect site. If such a defect site exists, cracking may occur even if the internal stress is relatively low.

  Although the scope of the present invention is not limited, it is presumed that the mechanism that causes cracks starting from the surface irregularities of the release surface of the polarizing plate is as follows. When unevenness sufficiently smaller than the thickness of the polarizer layer is present on the release surface, a protective film is bonded to the surface using an adhesive, or a glass substrate is bonded to the surface via an adhesive layer. In some cases, a gap that is too small to be detected by a human eye or a defect inspection device may be generated. Since the size of the gap is as small as several μm, it is considered that the polarizer layer portion forming the gap maintains the contraction stress of the polarizer layer as it is. On the other hand, since the portion where the void portion exists cannot enjoy the reinforcing effect by the protective film or the glass substrate via the adhesive layer or the pressure-sensitive adhesive layer, the portion exists as a weak portion particularly in the polarizing plate, It is thought that it is easy to become a starting point. Actually, when the cross section of the polarizing plate that has cracked is analyzed with a scanning electron microscope or the like, a gap of about several μm can be detected in the cracked portion. As described above, since this gap is not at a level that can be detected by human eyes or a defect inspection instrument, it is difficult to take measures such as eliminating a polarizing plate having a gap as a defective product. is there.

According to the present invention, by setting the arithmetic average roughness Ra ₀ of the substrate film surface on which the polarizer layer is formed to 130 nm or less, the arithmetic average roughness Ra ₁ of the release surface of the obtained polarizing plate is set to be polarizing. since the base film in the polarizer layer constituting the laminated film be close to the arithmetic average roughness Ra ₂ of the surface on the opposite side, that it is possible to reduce the arithmetic mean roughness Ra _1, the thickness of the polarizer layer For example, even a thin film having a thickness of 10 μm or less can suppress the generation of voids that are so small that they cannot be detected, and that are likely to be cracking starting points.

  In addition, when a polarizing plate is manufactured by forming a polarizer layer on a base film to obtain a polarizing laminate film, and then peeling and removing the base film after pasting a protective film on the polarizer layer, peeling is performed. It is inevitable that the surface state of the surface is affected by the surface state of the base film, and this point is also described in Patent Document 2. However, the invention described in Patent Document 2 is focused on foreign matters (dust etc.) and scratches which are present on the surface and inside of the base film and are large enough to be visually recognized. It is intended to construct a display device with the polarizer layer surface having unevenness and scratches facing away from the display cell. In addition, the invention described in Patent Document 2 has a problem in that the visibility of the display device is lowered due to unevenness and scratches on the polarizer layer rather than cracks in the polarizer layer, and bright spots. It does not provide a method for suppressing unevenness and scratches.

  In the first place, it has become clear from the study of the present inventor that a defect (for example, a foreign material) that is large enough to be visually recognized is not a defect site that provides a crack starting point. This is because defects of several tens of μm or more in the thin film (for example, 10 μm or less) polarizer layer are occupied by replacing most or all of the polarizer layer in the thickness direction of the polarizer layer, and the defect portion is polarized. Since there is almost no child layer, it is presumed that the contraction stress of the polarizer layer itself does not work at the defect portion or is very small. On the other hand, the minute surface unevenness of an invisible level of less than several tens of μm, which is the focus of the present invention (for example, a small surface unevenness of 50 μm or less and including nano-order minute surface unevenness) ) Can cause cracks in the heat shock test regardless of whether the surface is disposed on the glass substrate side or on the opposite side.

(1) 1st protective film bonding process S40
With reference to FIG. 5, in this step, the first protective film 10 is bonded to the surface of the polarizer layer 5 of the polarizing laminated film 300 opposite to the base film 30 ′ via the first adhesive layer 15. And it is a process of obtaining the polarizing laminated film 400 with a protective film. When the polarizing laminated film 300 has the polarizer layers 5 on both surfaces of the base film 30 ′, the protective films are usually bonded on the polarizer layers 5 on both surfaces. In this case, these protective films may be the same type of protective film or different types of protective films.

  The material constituting the first protective film 10 is preferably a light-transmitting (preferably optically transparent) thermoplastic resin. Examples of such a resin include a chain polyolefin resin (polypropylene resin). Resins), polyolefin resins such as cyclic polyolefin resins (norbornene resins, etc.); cellulose ester resins such as cellulose triacetate and cellulose diacetate; polyester resins; polycarbonate resins; (meth) acrylic resins; Examples thereof include polystyrene resins; or mixtures and copolymers thereof.

  The first protective film 10 can also be a protective film having an optical function such as a retardation film and a brightness enhancement film. For example, a retardation film provided with an arbitrary retardation value by stretching a film made of the thermoplastic resin (uniaxial stretching or biaxial stretching) or by forming a liquid crystal layer or the like on the film. It can be.

  Examples of the chain polyolefin-based resin include a homopolymer of a chain olefin such as a polyethylene resin and a polypropylene resin, and a copolymer composed of two or more chain olefins.

  Cyclic polyolefin resin is a general term for resins that are polymerized using a cyclic olefin as a polymerization unit. Specific examples of cyclic polyolefin resins include ring-opening (co) polymers of cyclic olefins, addition polymers of cyclic olefins, copolymers of cyclic olefins and chain olefins such as ethylene and propylene (typically Are random copolymers), graft polymers obtained by modifying them with unsaturated carboxylic acids or derivatives thereof, and hydrides thereof. Among these, norbornene resins using norbornene monomers such as norbornene and polycyclic norbornene monomers as cyclic olefins are preferably used.

  The cellulose ester resin is an ester of cellulose and a fatty acid. Specific examples of the cellulose ester resin include cellulose triacetate, cellulose diacetate, cellulose tripropionate, and cellulose dipropionate. Moreover, these copolymers and those in which a part of the hydroxyl group is modified with other substituents can also be used. Among these, cellulose triacetate (triacetyl cellulose: TAC) is particularly preferable.

  The polyester-based resin is a resin having an ester bond, and is generally made of a polycondensate of a polyvalent carboxylic acid or a derivative thereof and a polyhydric alcohol. As the polyvalent carboxylic acid or a derivative thereof, a divalent dicarboxylic acid or a derivative thereof can be used, and examples thereof include terephthalic acid, isophthalic acid, dimethyl terephthalate, and dimethyl naphthalenedicarboxylate. As the polyhydric alcohol, a divalent diol can be used, and examples thereof include ethylene glycol, propanediol, butanediol, neopentyl glycol, and cyclohexanedimethanol.

  Specific examples of the polyester resin include polyethylene terephthalate, polybutylene terephthalate, polyethylene naphthalate, polybutylene naphthalate, polytrimethylene terephthalate, polytrimethylene naphthalate, polycyclohexanedimethyl terephthalate, polycyclohexanedimethyl naphthalate.

  The polycarbonate resin is composed of a polymer in which monomer units are bonded via a carbonate group. The polycarbonate-based resin may be a resin called a modified polycarbonate having a modified polymer skeleton, a copolymer polycarbonate, or the like.

The (meth) acrylic resin is a resin containing a compound having a (meth) acryloyl group as a main constituent monomer. Specific examples of (meth) acrylic resins include, for example, poly (meth) acrylic acid esters such as polymethyl methacrylate; methyl methacrylate- (meth) acrylic acid copolymer; methyl methacrylate- (meth) acrylic acid Ester copolymer; methyl methacrylate-acrylic ester- (meth) acrylic acid copolymer; (meth) methyl acrylate-styrene copolymer (MS resin etc.); methyl methacrylate and alicyclic hydrocarbon group And a copolymer (for example, methyl methacrylate-cyclohexyl methacrylate copolymer, methyl methacrylate- (meth) acrylate norbornyl copolymer). Preferably, a polymer based on a poly (meth) acrylic acid C _1-6 alkyl ester such as poly (meth) acrylic acid methyl is used, and more preferably methyl methacrylate is the main component (50-100). % Methyl methacrylate resin is used.

  In addition, the description about each thermoplastic resin shown above is applicable also to the thermoplastic resin which comprises the base film 30. FIG.

  A surface treatment layer (coating layer) such as a hard coat layer, an antiglare layer, an antireflection layer, an antistatic layer and an antifouling layer is formed on the surface of the first protective film 10 opposite to the polarizer layer 5. You can also The method for forming the surface treatment layer on the surface of the protective film is not particularly limited, and a known method can be used.

  Although it is preferable that the thickness of the 1st protective film 10 is thin from a viewpoint of thickness reduction of a polarizing plate, when too thin, intensity | strength will fall and it will be inferior to workability. Therefore, the thickness of the first protective film 10 is preferably 5 to 90 μm or less, more preferably 5 to 60 μm, and still more preferably 5 to 50 μm. Even if the thickness of the 1st protective film 10 is 30 micrometers or less, according to this invention, the crack of the polarizer layer in a heat shock test can be suppressed effectively.

  As an adhesive that forms the first adhesive layer 15, for example, a water-based adhesive or a photocurable adhesive can be used. Examples of the water-based adhesive include an adhesive made of a polyvinyl alcohol-based resin aqueous solution, an aqueous two-component urethane emulsion adhesive, and the like. In particular, when a cellulose ester resin film that has been surface-treated (hydrophilized) by saponification treatment or the like is used as the first protective film 10, it is preferable to use a water-based adhesive comprising a polyvinyl alcohol-based resin aqueous solution.

  Polyvinyl alcohol resins include vinyl alcohol homopolymers obtained by saponifying polyvinyl acetate, which is a homopolymer of vinyl acetate, and copolymers of vinyl acetate and other monomers copolymerizable therewith. A polyvinyl alcohol copolymer obtained by saponifying the polymer or a modified polyvinyl alcohol polymer obtained by partially modifying the hydroxyl group thereof can be used. The water-based adhesive can contain additives such as polyvalent aldehydes, water-soluble epoxy compounds, melamine compounds, zirconia compounds, and zinc compounds.

  A water-based adhesive is applied to the bonding surface of the polarizer layer 5 and / or the first protective film 10 of the polarizing laminated film 300, and these films are bonded via the adhesive layer, preferably a bonding roll. A pasting process is carried out by applying pressure and making close contact with each other. The coating method of the water-based adhesive (same for the photo-curable adhesive) is not particularly limited, and casting method, Meyer bar coating method, gravure coating method, comma coater method, doctor plate method, die coating method, dip coating method A conventionally known method such as a spraying method can be used.

  When using an aqueous adhesive, it is preferable to implement the drying process which dries a film in order to remove the water contained in an aqueous adhesive after implementing the above-mentioned bonding. Drying can be performed, for example, by introducing the film into a drying furnace. The drying temperature (temperature of the drying furnace) is preferably 30 to 90 ° C. There exists a tendency for the 1st protective film 10 to become easy to peel from the polarizer layer 5 as it is less than 30 degreeC. If the drying temperature exceeds 90 ° C., the polarization performance of the polarizer layer 5 may be deteriorated by heat. The drying time can be about 10 to 1000 seconds, and from the viewpoint of productivity, it is preferably 60 to 750 seconds, and more preferably 150 to 600 seconds.

  After the drying step, a curing step of curing at room temperature or slightly higher temperature, for example, at a temperature of about 20 to 45 ° C. for about 12 to 600 hours may be provided. The curing temperature is generally set lower than the drying temperature.

  The photocurable adhesive refers to an adhesive that is cured by irradiating light such as ultraviolet rays, for example, an adhesive containing a polymerizable compound and a photopolymerization initiator, an adhesive containing a photoreactive resin, a binder resin, and The thing containing a photoreactive crosslinking agent etc. can be mentioned. Examples of the polymerizable compound include photopolymerizable monomers such as a photocurable epoxy monomer, a photocurable acrylic monomer, and a photocurable urethane monomer, and oligomers derived from the photopolymerizable monomer. As a photoinitiator, what contains the substance which generate | occur | produces active species, such as a neutral radical, an anion radical, and a cation radical by irradiation of light like an ultraviolet-ray can be mentioned. As the photocurable adhesive containing a polymerizable compound and a photopolymerization initiator, an adhesive containing a photocurable epoxy monomer and a photocationic polymerization initiator can be preferably used.

  When using a photocurable adhesive, after carrying out the above-mentioned bonding, a drying step is performed as necessary (such as when the photocurable adhesive contains a solvent), and then photocurable by irradiating light. A curing step for curing the adhesive is performed. The light to be irradiated is not particularly limited, but preferably has a light emission distribution at a wavelength of 400 nm or less. Specifically, the light source is a low pressure mercury lamp, a medium pressure mercury lamp, a high pressure mercury lamp, an ultrahigh pressure mercury lamp, a chemical lamp, a black light lamp, a micro lamp. A wave excitation mercury lamp, a metal halide lamp, etc. are preferably used.

  In bonding the first protective film 10 on the polarizer layer 5, the bonding surface of the first protective film 10 is subjected to plasma treatment, corona treatment, ultraviolet ray in order to improve the adhesion with the polarizer layer 5. Surface treatment (easy adhesion treatment) such as irradiation treatment, flame (flame) treatment, and saponification treatment can be performed, and among them, plasma treatment, corona treatment or saponification treatment is preferable. For example, when the first protective film 10 is made of a cyclic polyolefin resin, plasma treatment or corona treatment is usually performed. Moreover, when it consists of a cellulose ester-type resin, a saponification process is normally performed. Examples of the saponification treatment include a method of immersing in an alkaline aqueous solution such as sodium hydroxide or potassium hydroxide.

(2) Peeling step S50
With reference to FIG. 6, this process is a process which peels and removes base-material film 30 'after 1st protective film bonding process S40. In this step, the polarizing plate 1 with a single-side protective film is obtained. When the polarizing laminated film 300 has the polarizer layers 5 on both surfaces of the base film 30 ′, and a protective film is bonded to both the polarizer layers 5, a single polarized light is obtained by the peeling step S 50. The polarizing plate 1 with a single-sided protective film is obtained from the conductive laminated film 300.

  The method for peeling and removing the base film 30 ′ is not particularly limited, and can be peeled by the same method as the separator (peeling film) peeling step performed with a normal pressure-sensitive adhesive polarizing plate. The base film 30 ′ may be peeled off immediately after the first protective film bonding step S40, or is wound up into a roll once after the first protective film bonding step S40 and wound in the subsequent steps. You may peel off while taking out.

According to the present invention, the polarizing laminated film 300 is manufactured using the base film 30 having the arithmetic average roughness Ra ₀ of 130 nm or less on the surface on which the polarizer layer 5 is formed, and the polarizing plate is formed using this. In order to manufacture, the arithmetic average roughness Ra _{1 of} the release surface is close to the arithmetic average roughness Ra ₂ of the surface opposite to the base film 30 ′ in the polarizer layer 5 constituting the polarizing laminated film 300, that is, arithmetic. it is possible to obtain a small one surface protective film with the polarizing plate 1 average roughness Ra _1. This polarizing plate 1 with a single-sided protective film is less likely to crack in the heat shock test, and has high durability against a rapid temperature difference.

From the viewpoint of effectively suppressing cracks, the difference between the arithmetic average roughness Ra ₁ and the arithmetic average roughness Ra ₂ is preferably 15 nm or less in absolute value, and more preferably 12 nm or less. For the same reason, the arithmetic average roughness Ra ₁ is preferably 55 nm or less, and more preferably 50 nm or less.

<2nd protective film bonding process S50>
With reference to FIG.1 and FIG.7, if this process of bonding the 2nd protective film 20 to the peeling surface of the polarizing plate 1 with a single-sided protective film through the 2nd adhesive bond layer 25 is implemented, with a double-sided protective film The polarizing plate 2 can be obtained. This polarizing plate 2 with a double-sided protective film is also less likely to crack in the heat shock test and has high durability against a sudden temperature difference.

  About the 2nd protective film 20 and the 2nd adhesive bond layer 25 which bonds this, the description which described the 1st protective film 10 and the 1st adhesive bond layer 15 is quoted. The first protective film 10 and the second protective film 20 may be the same type of protective film or different types of protective films. The 1st adhesive bond layer 15 and the 2nd adhesive bond layer 25 may be formed from the mutually same kind of adhesive agent, and may be formed from a different kind of adhesive agent.

  The polarizing plate 1 with a single-sided protective film and the polarizing plate 2 with a double-sided protective film obtained as described above can be used as a composite polarizing plate by bonding peripheral members together. it can. As the peripheral member, a protective film for preventing scratches bonded on the protective film; on the protective film (for example, in the case of the polarizing plate 2 with a double-sided protective film) or on the polarizer layer 5 (for example, with a single-sided protective film) Adhesive layer for laminating a polarizing plate to a display cell or other optical member; a separate film laminated on the outer surface of the adhesive layer; In the case of the polarizing plate 2 with a protective film) or on the polarizer layer 5 (for example, in the case of the polarizing plate 1 with a single-side protective film), an optical compensation film such as a retardation film, or other optical functional film. Is mentioned.

  The pressure-sensitive adhesive layer as an example of the peripheral member can be laminated on the outer surface of one of the protective films in the double-sided protective film-attached polarizing plate 2, and the single-sided protective film-attached polarizing plate 1 is, for example, peeled It can be laminated to the surface. The pressure-sensitive adhesive forming the pressure-sensitive adhesive layer is usually based on a (meth) acrylic resin, styrene resin, silicone resin or the like, and a crosslinking agent such as an isocyanate compound, an epoxy compound, or an aziridine compound is added thereto. It consists of an adhesive composition. Furthermore, it can also be set as the adhesive layer which contains microparticles | fine-particles and shows light-scattering property. The thickness of an adhesive layer is 1-40 micrometers normally, Preferably it is 3-25 micrometers.

  In addition, as an optical functional film as another example of the peripheral member, a reflective polarizing film that transmits a certain kind of polarized light and reflects polarized light that shows the opposite property; anti-glare having an uneven shape on the surface A film with a function; a film with a surface antireflection function; a reflection film having a reflection function on the surface; a transflective film having both a reflection function and a transmission function; and a viewing angle compensation film.

  EXAMPLES Hereinafter, although an Example and a comparative example are shown and this invention is demonstrated further more concretely, this invention is not limited by these examples.

  In the following examples and comparative examples, the arithmetic average roughness Ra is obtained by obtaining a surface image using PLμ2300 sold by Senso Co., Ltd., and then statistically processing it using the attached software. It was. The lens was 20 times, and the observation area was 636.61 μm × 477.25 μm.

<Example 1>
(1) Production of base film Both surfaces of a resin layer comprising a random copolymer of propylene / ethylene containing about 5% by weight of ethylene units (“Sumitomo Noblen W151” manufactured by Sumitomo Chemical Co., Ltd., melting point Tm = 138 ° C.) A base film having a three-layer structure in which a resin layer made of homopolypropylene (“Sumitomo Nobrene FLX80E4” manufactured by Sumitomo Chemical Co., Ltd., melting point Tm = 163 ° C.), which is a homopolymer of propylene, It was produced by coextrusion molding using The total thickness of the base film was 90 μm, and the thickness ratio (FLX80E4 / W151 / FLX80E4) of each layer was 3/4/3. No nucleating agent was used.

Since the resin melting temperature at the time of co-extrusion was 275 ° C. and the temperature of the chill roll used for cooling the molten film was 25 ° C., the temperature difference during cooling was 250 ° C. The base film surface on the side where the polyvinyl alcohol-based resin layer is formed had an arithmetic average roughness Ra ₀ of 55.0 nm.

(2) Primer layer forming step Polyvinyl alcohol powder (“Z-200” manufactured by Nippon Synthetic Chemical Industry Co., Ltd., average polymerization degree 1100, saponification degree 99.5 mol%) is dissolved in 95 ° C. hot water, A polyvinyl alcohol aqueous solution having a concentration of 3% by weight was prepared. The resulting aqueous solution was mixed with a crosslinking agent (“Smiles Resin 650” manufactured by Taoka Chemical Co., Ltd.) at a ratio of 5 parts by weight to 6 parts by weight of the polyvinyl alcohol powder to form a primer layer forming coating solution. Got.

Next, after corona treatment was performed on one side of the base film prepared in the above (1) (a surface having an arithmetic average roughness Ra ₀ of 55.0 nm), the above-described corona treatment surface was subjected to the above using a micro gravure coater. The primer layer-forming coating solution was applied and dried at 80 ° C. for 10 minutes to form a primer layer having a thickness of 0.2 μm.

(3) Production of laminated film (resin layer forming step)
Polyvinyl alcohol powder (“PVA124” manufactured by Kuraray Co., Ltd., average polymerization degree 2400, saponification degree 98.0 to 99.0 mol%) was dissolved in hot water at 95 ° C., and a polyvinyl alcohol aqueous solution having a concentration of 8% by weight. This was used as a coating liquid for forming a polyvinyl alcohol resin layer.

  By applying the polyvinyl alcohol-based resin layer forming coating solution to the primer layer surface of the base film having the primer layer prepared in (2) above using a lip coater, and then drying at 80 ° C. for 20 minutes. A polyvinyl alcohol-based resin layer was formed on the primer layer to obtain a laminated film composed of base film / primer layer / polyvinyl alcohol-based resin layer.

(4) Production of stretched film (stretching process)
The laminated film produced in the above (3) was subjected to 5.8-fold free end uniaxial stretching at 160 ° C. using a floating longitudinal uniaxial stretching apparatus to obtain a stretched film. The thickness of the stretched polyvinyl alcohol resin layer was 6.2 μm.

(5) Preparation of polarizing laminated film (dyeing process)
The stretched film prepared in the above (4) is about 30 ° C. dyed aqueous solution containing iodine and potassium iodide (0.6 parts by weight of iodine and 10 parts by weight of potassium iodide per 100 parts by weight of water). After the polyvinyl alcohol resin layer was dyed for 180 seconds, the excess dye solution was washed away with pure water at 10 ° C.

  Next, it is immersed for 120 seconds in a first crosslinked aqueous solution of 78 ° C. containing boric acid (containing 9.5 parts by weight of boric acid per 100 parts by weight of water), and then 70 ° C. containing boric acid and potassium iodide. A crosslinking treatment was performed by immersing in a second aqueous crosslinking solution (containing 9.5 parts by weight of boric acid and 4 parts by weight of potassium iodide per 100 parts by weight of water) for 60 seconds. Thereafter, the film was washed with pure water at 10 ° C. for 10 seconds, and finally dried at 40 ° C. for 300 seconds to obtain a polarizing laminated film comprising a base film / primer layer / polarizer layer.

In the obtained light-polarizing laminated film, the arithmetic average roughness Ra ₂ of the surface on the side opposite to the base film in the polarizer layer was measured and found to be 38.5 nm.

(6) Preparation of polarizing plate (protective film bonding step and peeling step)
Polyvinyl alcohol powder (“KL-318” manufactured by Kuraray Co., Ltd., average polymerization degree 1800) was dissolved in hot water at 95 ° C. to prepare a polyvinyl alcohol aqueous solution having a concentration of 3% by weight. The resulting aqueous solution was mixed with a crosslinking agent (“Smile Resin 650” manufactured by Taoka Chemical Co., Ltd.) at a ratio of 1 part by weight to 2 parts by weight of the polyvinyl alcohol powder to obtain an aqueous adhesive solution.

  Next, after coating the adhesive aqueous solution on the surface opposite to the base film in the polarizer layer of the polarizing laminate film prepared in the above (5), a protective film [consisting of triacetyl cellulose (TAC) is used. A transparent protective film (“KC4UY” manufactured by Konica Minolta Opto Co., Ltd.), thickness 40 μm] is pasted and dried in an oven at 80 ° C. for 2 minutes to form a base film / primer layer / polarizer layer / adhesive layer / The polarizing laminated film with a protective film which consists of protective films was obtained.

  Subsequently, the base film was peeled off from the polarizing laminated film with a protective film. The base film was easily peeled off to obtain a polarizing plate with a single-side protective film. The thickness of the polarizer layer was 6.7 μm.

In the obtained one-side protective film-attached polarizing plate was measured for the arithmetic average roughness Ra ₁ of the release surface revealed by peeling removal of the base film was 38.7Nm. Finally, an acrylic pressure-sensitive adhesive layer was provided on the release surface to obtain a polarizing plate with a pressure-sensitive adhesive layer.

<Example 2>
A base film was prepared in the same manner as in Example 1 except that 1% by weight of a nucleating agent consisting of high-density polyethylene was added to two homopolypropylene layers serving as surface layers with respect to the homopolypropylene. A polarizing plate with an adhesive layer was produced in the same manner as in Example 1 except that was used.

<Example 3>
A base film was prepared in the same manner as in Example 1 except that a nucleating agent composed of high-density polyethylene was added to two homopolypropylene layers serving as surface layers with respect to the homopolypropylene. A polarizing plate with an adhesive layer was produced in the same manner as in Example 1 except that was used.

<Comparative Example 1>
A base film was prepared in the same manner as in Example 3 except that the resin melting temperature at the time of coextrusion was 265 ° C., and with the adhesive layer as in Example 1 except that this base film was used. A polarizing plate was produced.

<Comparative example 2>
A base film was prepared in the same manner as in Comparative Example 1 except that 3 wt% of a nucleating agent consisting of high-density polyethylene was added to the two homopolypropylene layers as the surface layer with respect to the homopolypropylene. A polarizing plate with an adhesive layer was produced in the same manner as in Example 1 except that was used.

<Comparative Example 3>
A base film was prepared in the same manner as in Comparative Example 2 except that the resin melting temperature at the time of co-extrusion was 260 ° C., and with the adhesive layer as in Example 1 except that this base film was used. A polarizing plate was produced.

Table 1 summarizes the addition amount of the nucleating agent during the production of the base film, the temperature difference during cooling, and the arithmetic average roughness Ra ₀ , Ra ₁ and Ra ₂ .

[Heat shock test]
The polarizing plates obtained in Examples and Comparative Examples were chip-cut to 4.4 "size (50 mm x 100 mm), and this was bonded to Corning glass using the adhesive layer. Prepare a sheet, put them in a thermal shock tester, and after “holding in a −40 ° C. bath for 30 minutes, immediately transfer to 85 ° C. bath and hold for 30 minutes” as one cycle, this is 400 cycles Repeated heat shock tests were performed. The number of cracks in the polarizer layer in 50 samples was visually counted, and the number of cracks was converted to the number per 1 m ² . Samples were taken out during 100 cycles and 250 cycles during the test, and the number of cracks per 1 m ² was determined in the same manner. The results are shown in Table 1.

  Even if a heat shock test was performed in the same manner as above to provide a polarizing plate with an adhesive layer by providing an acrylic adhesive layer on the protective film side of the obtained polarizing plate with a single-side protective film, These were substantially the same as Examples 1 to 3 and Comparative Examples 1 to 3, respectively.

  DESCRIPTION OF SYMBOLS 1 Polarizing plate with single-sided protective film, 2 Polarizing plate with double-sided protective film, 5 Polarizer layer, 6 Polyvinyl alcohol-type resin layer, 6 'Stretched polyvinyl alcohol-type resin layer, 10 1st protective film, 15 1st adhesive agent Layer, 20 second protective film, 25 second adhesive layer, 30 base film, 30 ′ stretched base film, 100 laminated film, 200 stretched film, 300 polarizing laminated film, 400 polarizing laminate with protective film the film.

Claims (9)

A method for producing a polarizing plate comprising a step of producing a polarizing laminated film,
The step of producing the polarizing laminated film comprises:
Forming a polyvinyl alcohol resin layer on the base film surface to obtain a laminated film;
A step of obtaining a stretched film by uniaxially stretching a free end so that the laminated film is more than 5 times the original length of the laminated film;
A step of obtaining a polarizing laminated film by dyeing a polyvinyl alcohol-based resin layer of the stretched film with a dichroic dye to form a polarizer layer;
Including
The manufacturing method of the polarizing plate is as follows:
Producing the polarizing laminated film; and
A step of bonding a first protective film to a surface of the polarizer layer opposite to the base film;
Peeling and removing the base film;
In this order,
The arithmetic average roughness Ra ₀ of the front side of the side of the base film of polyvinyl alcohol-based resin layer is formed is not more than 130 nm,
The polyvinyl alcohol-based resin layer is formed by applying a coating liquid containing a polyvinyl alcohol-based resin ,
The arithmetic average roughness Ra ₀ is a method of manufacturing a polarizing plate, which is a value calculated based on a surface image obtained by a confocal microscope . The manufacturing method according to claim 1, wherein the base film has a single-layer structure composed of one resin layer or a multilayer structure in which a plurality of resin layers are stacked. Ri der arithmetic average roughness Ra ₁ is 55nm or less of the surface which appears by peeling removal of the base film in a polarizing plate obtained by separating and removing the substrate film,
3. The method according to claim 1, wherein the arithmetic average roughness Ra ₁ is a value calculated based on a surface image obtained by a confocal microscope . In the polarizing plate obtained by peeling and removing the base film, the arithmetic average roughness Ra _{1 of the} surface appearing by peeling and removing the base film, and the base film in the polarizer layer constituting the polarizing laminated film difference der 15nm or less at an absolute value of the arithmetic average roughness Ra ₂ of the opposite surface is,
The arithmetic average roughness Ra ₁ and Ra ₂ is a value calculated on the basis of the surface image obtained by confocal microscopy method as claimed in any one of claims 1-3. The manufacturing method of any one of Claims 1-4 whose thickness of the polarizer layer which comprises the said polarizing laminated film is 10 micrometers or less. The manufacturing method according to any one of claims 1 to 5 , wherein the first protective film is a thermoplastic resin film. Further comprising the step of laminating a second protective film made of a thermoplastic resin on the surface which appears by peeling removal of the base film in a polarizing plate obtained by separating and removing the substrate film, any one of claims 1 to 6 2. The production method according to item 1. The polarization further comprises at least one surface of the optical plate laminating a pressure-sensitive adhesive layer, the manufacturing method according to any one of claims 1-7. The process of obtaining the polarizing plate manufactured with the manufacturing method of any one of Claims 1-8 ,
Manufacturing a display device comprising the polarizing plate.

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