JP2014085616A - Manufacturing method of polarizable laminate film and manufacturing method of polarizing plate - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a method for manufacturing a polarizable laminate film or a polarizing plate with excellent material yield, the method capable of drawing a laminate film in which a polyvinyl alcohol resin layer is formed on a base film by coating, while suppressing wrinkle generation or uneven drawing, and having excellent appearance and optical characteristic.SOLUTION: A manufacturing method of a polarizable laminate film includes: a resin layer formation process of applying a coating slip including a polyvinyl alcohol resin on a base film to obtain a laminate film; a drawing process of vertically and uniaxial drawing the laminate film to obtain a drawn film; and a dyeing process of dyeing the polyvinyl alcohol resin layer of the drawn film by a dichroic dye to obtain a polarizer layer. The drawing process includes two or more stages of drawing processing processes. A ratio of draw magnification in the drawing processing process of a first stage to draw magnification in the drawing processing process of the second stage is 0.5 or more. The total draw magnification of the polarizer layer is five times or more. There is also provided a manufacturing method of a polarizing plate using a polarizable laminate film obtainable by the method.

Description

  The present invention relates to a method for producing a polarizing laminate film and a method for producing a polarizing plate.

  The polarizing plate is widely used as a polarized light supplying element and a polarized light detecting element in a liquid crystal display device. Conventionally, as a polarizing plate, a polarizing film made of a polyvinyl alcohol resin and a protective film made of triacetyl cellulose or the like bonded to an adhesive is used. With the development of mobile devices such as personal computers and mobile phones, as well as the development of large televisions, there is a demand for thinner and lighter polarizing plates.

  However, the polarizing film is produced by stretching and dyeing a polyvinyl alcohol-based resin film (usually about 75 μm thick), and the thickness of the stretched film is usually about 30 μm. Thinning beyond this has been difficult due to productivity problems such as the film during stretching being easily broken.

  Then, after forming the polyvinyl alcohol-type resin layer by coating the coating liquid containing polyvinyl alcohol-type resin on a base film and obtaining a laminated film, extending | stretching and dyeing | staining process are performed with respect to this laminated film Thus, there has been proposed a method for producing a laminated film (polarizing plate) having a polarizer layer that imparts a polarizing function to a polyvinyl alcohol-based resin layer to form a polarizer layer (for example, Patent Documents 1 to 3).

JP 2009-93074 A JP 2011-150313 A JP 2012-159778 A

  According to the method of forming a polarizer layer by coating a coating liquid containing a polyvinyl alcohol resin as described in Patent Documents 1 to 3, a polarizing film is produced from the original film of the polyvinyl alcohol resin. Since a thinner polarizer layer can be obtained, it is advantageous from the viewpoint of reducing the thickness and weight of the polarizing plate.

  However, when a laminated film having a polyvinyl alcohol-based resin layer is stretched, wrinkles are generated in the stretched film, or stretching unevenness (non-uniform stretching) occurs in the film width direction. There was a problem that unevenness in thickness occurred in the film width direction.

  Therefore, an object of the present invention is to form a polyvinyl alcohol resin layer by coating a base film with a coating liquid containing a polyvinyl alcohol resin, to obtain a laminated film, and then by stretching and dyeing the laminated film. In the method for producing a polarizing laminated film or polarizing plate using a polyvinyl alcohol-based resin layer as a polarizer layer, the laminated film can be stretched while suppressing wrinkles and stretching unevenness, and thus the appearance and optical properties of An object of the present invention is to provide a method capable of producing a good polarizing laminate film or polarizing plate with a high yield.

The present invention includes the following.
[1] A resin layer forming step of forming a polyvinyl alcohol-based resin layer by applying a coating liquid containing a polyvinyl alcohol-based resin on at least one surface of a base film and then drying to form a laminated film; ,
Stretching process for obtaining a stretched film by longitudinally uniaxially stretching the laminated film,
A dyeing 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;
The stretching step includes two or more stretching treatment steps,
The ratio of the stretching ratio in the first stretching process to the stretching ratio in the second stretching process is 0.5 or more,
The method for producing a polarizing laminated film, wherein the total draw ratio of the polarizer layer is more than 5 times based on the polyvinyl alcohol resin layer of the laminated film.

  [2] The method for producing a polarizing laminated film according to [1], wherein in the resin layer forming step, the polyvinyl alcohol-based resin layer is formed on both surfaces of the base film.

  [3] The method for producing a polarizing laminated film according to [1] or [2], wherein the thickness of the polyvinyl alcohol-based resin layer of the laminated film is 3 to 30 μm.

  [4] The method for producing a polarizing laminated film according to any one of [1] to [3], wherein a stretching ratio in the first stretching process step is less than 5 times.

  [5] The method for producing a polarizing laminated film according to any one of [1] to [4], wherein the base film is made of a polypropylene resin.

[6] A step of preparing a polarizing laminated film obtained by the production method according to any one of [1] to [5];
A step of bonding a protective film on the polarizer layer of the polarizing laminate film to obtain a bonding film;
A step of peeling the base film from the bonding film;
The manufacturing method of a polarizing plate provided with.

  According to the method of the present invention, the occurrence of wrinkles and stretching unevenness in the film width direction during the stretching of the laminated film (thus, thickness unevenness in the film width direction) can be effectively suppressed. A good polarizing laminate film or polarizing plate can be produced with good yield.

It is a flowchart which shows preferable embodiment of 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 diagram which shows an example of the multistage extending | stretching in extending process S20. It is a schematic diagram which shows another example of the multistage extending | stretching in extending process S20. It is a schematic diagram for demonstrating the longitudinal uniaxial stretching system using a chuck | zipper.

  Hereinafter, an embodiment is shown and the manufacturing method of the light-polarizing laminated film concerning the present invention and the manufacturing method of a polarizing plate are explained in detail.

<Method for producing polarizing laminated film>
FIG. 1 is a flowchart showing a preferred embodiment of a method for producing a polarizing laminate film and a method for producing a polarizing plate according to the present invention. The manufacturing method of the light-polarizing laminated film of this embodiment includes the following steps:
Resin layer forming step S10 to obtain a laminated film by forming a polyvinyl alcohol-based resin layer by applying a coating liquid containing a polyvinyl alcohol-based resin on at least one surface of the base film, followed by drying.
Stretching step S20 to obtain a stretched film by uniaxially stretching the laminated 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,
Are included in this order.

  As will be described later, in the present embodiment, the polarizing plate is bonded to a protective film on the polarizer layer of the polarizing laminate film obtained by carrying out the dyeing step S30 (bonding step S40). ), And then the substrate film is peeled and removed from the bonded film (peeling step S50).

  Hereinafter, each process of S10-S30 with which the manufacturing method of the light-polarizing laminated film of this embodiment is provided is demonstrated in detail.

[1] Resin layer forming step S10
This step is a step of obtaining a laminated film by forming a polyvinyl alcohol-based resin layer on at least one surface of the base film. This polyvinyl alcohol-based resin layer is a layer that becomes a polarizer layer through the stretching step S20 and the dyeing step S30. A polyvinyl alcohol-type resin layer can be formed by applying the coating liquid containing a polyvinyl alcohol-type resin to the single side | surface or both surfaces of a base film, and drying a coating layer. According to such a method, the thickness of the polyvinyl alcohol-based resin layer and thus the polarizer layer can be reduced, which is advantageous for reducing the thickness and weight of the polarizing laminated film and the polarizing plate.

(Base film)
The base film can be composed of a thermoplastic resin, and among them, it is preferably composed of a thermoplastic resin 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 may have a single-layer structure composed of one resin layer composed of one or two or more thermoplastic resins, or a plurality of resin layers composed of one or two or more thermoplastic resins are laminated. It may be a multilayer structure.

  Examples of the chain polyolefin-based resin include homopolymers of chain olefins such as polyethylene resins and polypropylene resins, and copolymers composed of two or more chain olefins. A base film made of a chain polyolefin-based resin is preferable in that it is easily stretched stably at a high magnification. Among them, the base film is composed mainly of polypropylene resin (polypropylene resin which is a homopolymer of propylene or a copolymer mainly composed of propylene), polyethylene resin (polyethylene resin which is a homopolymer of ethylene or ethylene). It is more preferable to consist of a copolymer).

  A copolymer mainly composed of propylene, which is one of the examples suitably used as the thermoplastic resin constituting the base film, is a copolymer of propylene and another monomer copolymerizable therewith.

  Examples of other monomers copolymerizable with propylene include ethylene and α-olefin. As the α-olefin, an α-olefin having 4 or more carbon atoms is preferably used, and more preferably an α-olefin having 4 to 10 carbon atoms. Specific examples of the α-olefin having 4 to 10 carbon atoms include, for example, linear monoolefins such as 1-butene, 1-pentene, 1-hexene, 1-heptene, 1-octene and 1-decene; 3 -Branched monoolefins such as methyl-1-butene, 3-methyl-1-pentene, 4-methyl-1-pentene; and vinylcyclohexane. The copolymer of propylene and other monomers copolymerizable therewith may be a random copolymer or a block copolymer.

  Content of the said other monomer is 0.1-20 weight% in a copolymer, for example, Preferably it is 0.5-10 weight%. The content of other monomers in the copolymer can be determined by measuring infrared (IR) spectrum according to the method described on page 616 of "Polymer Analysis Handbook" (1995, published by Kinokuniya Shoten). Can be sought.

  Among these, as the polypropylene resin, a propylene homopolymer, a propylene-ethylene random copolymer, a propylene-1-butene random copolymer or a propylene-ethylene-1-butene random copolymer is preferably used.

  It is preferable that the stereoregularity of the polypropylene resin is substantially isotactic or syndiotactic. A base film made of a polypropylene-based resin having substantially isotactic or syndiotactic stereoregularity has relatively good handleability and excellent mechanical strength in a high temperature environment.

  The base film may be composed of one type of chain polyolefin-based resin, may be composed of a mixture of two or more types of chain polyolefin-based resins, or may be composed of two or more types of chain polyolefin-based resins. You may be comprised from the copolymer of resin.

  The cyclic polyolefin resin is a general term for resins that are polymerized using a cyclic olefin as a polymerization unit, and is described, for example, in JP-A-1-240517, JP-A-3-14882, JP-A-3-122137, and the like. Resin. 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.

  Various products are commercially available for the cyclic polyolefin resin. Examples of commercial products of cyclic polyolefin resins are trade names, “Topas” (manufactured by TOPAS ADVANCED POLYMERS GmbH, available from Polyplastics), “Arton” (manufactured by JSR), Includes “ZEONOR” (manufactured by Nippon Zeon Co., Ltd.), “ZEONEX” (manufactured by Nippon Zeon Co., Ltd.), and “Apel” (manufactured by Mitsui Chemicals, Inc.).

  In addition, film names such as “ESCINA” (manufactured by Sekisui Chemical Co., Ltd.), “SCA40” (manufactured by Sekisui Chemical Co., Ltd.), “ZEONOR FILM” (manufactured by ZEON Corporation) You may use the commercial item of the made cyclic polyolefin resin film as a base film.

  The base film may be composed of one kind of cyclic polyolefin-based resin, may be composed of a mixture of two or more kinds of cyclic polyolefin-based resins, or may be composed of two or more kinds of cyclic polyolefin-based resins. It may be composed of a polymer.

  The polyester 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.

  A typical example of the polyester resin is polyethylene terephthalate which is a polycondensate of terephthalic acid and ethylene glycol. Polyethylene terephthalate is a crystalline resin, but the one in a state before crystallization treatment is more easily subjected to treatment such as stretching. If necessary, it can be crystallized during stretching or by heat treatment after stretching. Further, a copolymerized polyester having a crystallinity lowered (or made amorphous) by further copolymerizing another monomer with a polyethylene terephthalate skeleton is also preferably used. Examples of such resins include those obtained by copolymerizing cyclohexanedimethanol and isophthalic acid. Since these resins are also excellent in stretchability, they can be suitably used.

  Specific examples of polyester resins other than polyethylene terephthalate and copolymers thereof include, for example, polybutylene terephthalate, polyethylene naphthalate, polybutylene naphthalate, polytrimethylene terephthalate, polytrimethylene naphthalate, polycyclohexanedimethyl terephthalate. And polycyclohexanedimethyl naphthalate.

  The base film may be composed of one kind of polyester resin, may be composed of a mixture of two or more kinds of polyester resins, or may be composed of a copolymer of two or more kinds of polyester resins. It may be configured.

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.

  The base film may be composed of one (meth) acrylic resin, may be composed of a mixture of two or more (meth) acrylic resins, or may be composed of two or more (meth) acrylic resins. ) It may be composed of a copolymer of acrylic resin.

  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 another substituent are also included. Among these, cellulose triacetate (triacetyl cellulose) is particularly preferable. Many products of cellulose triacetate are commercially available, which is advantageous in terms of availability and cost. Examples of commercially available cellulose triacetate are “Fujitac TD80” (manufactured by Fuji Film Co., Ltd.), “Fujitac TD80UF” (manufactured by Fuji Film Co., Ltd.), “Fujitac TD80UZ” (Fuji Film ( Co., Ltd.), “Fujitac TD40UZ” (Fuji Film Co., Ltd.), “KC8UX2M” (Konica Minolta Opto Co., Ltd.), “KC4UY” (Konica Minolta Opto Co., Ltd.), and the like.

  The base film may be composed of one kind of cellulose ester resin, may be composed of a mixture of two or more kinds of cellulose ester resins, or may be composed of two or more kinds of cellulose ester resins. It may be composed of a polymer.

  The polycarbonate-based resin is an engineering plastic made of a polymer in which monomer units are bonded via a carbonate group, and is a resin having high impact resistance, heat resistance, flame retardancy, and transparency. The polycarbonate-based resin constituting the base film may be a resin called a modified polycarbonate in which the polymer skeleton is modified in order to lower the photoelastic coefficient, a copolymer polycarbonate having improved wavelength dependency, or the like.

  Various products are commercially available for polycarbonate resins. Examples of commercially available polycarbonate-based resins are all “Panlite” (manufactured by Teijin Chemicals Ltd.), “Iupilon” (manufactured by Mitsubishi Engineering Plastics), “SD Polyca” (Sumitomo Dow). (Manufactured by Dow Chemical Co., Ltd.).

  The base film may be composed of one type of polycarbonate-based resin, may be composed of a mixture of two or more types of polycarbonate-based resins, or may be composed of a copolymer of two or more types of polycarbonate-based resins. It may be configured.

  Arbitrary appropriate additives other than said thermoplastic resin may be added to the base film. Examples of such additives include ultraviolet absorbers, antioxidants, lubricants, plasticizers, mold release agents, anti-coloring agents, flame retardants, nucleating agents, antistatic agents, pigments, and coloring agents. . The content of the thermoplastic resin in the base film is preferably 50 to 100% by weight, more preferably 50 to 99% by weight, still more preferably 60 to 98% by weight, and particularly preferably 70 to 97% by weight. When the content of the thermoplastic resin in the base film is less than 50% by weight, the high transparency inherent in the thermoplastic resin may not be sufficiently exhibited.

  The thickness of the base film can be determined as appropriate, but generally 1 to 500 μm is preferable, 1 to 300 μm is more preferable, 5 to 200 μm is more preferable, and 5 to 150 μm is preferable from the viewpoint of workability such as strength and handleability. Is most preferred.

(Coating liquid containing polyvinyl alcohol resin)
The coating liquid is preferably a polyvinyl alcohol resin solution obtained by dissolving a polyvinyl alcohol resin powder in a good solvent (for example, water). Examples of the polyvinyl alcohol resin include polyvinyl alcohol resins and derivatives thereof. Polyvinyl alcohol resin derivatives 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 a preferable polarization performance, and if it exceeds 10,000, the solubility in a solvent is deteriorated, and it becomes difficult to form a polyvinyl alcohol-based resin layer.

  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, the water resistance and heat-and-moisture resistance may not be sufficient when a polarizing laminate film or a polarizing plate is formed. 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 higher the degree of saponification, the greater the proportion of hydroxyl groups, and hence the smaller the proportion of acetate groups that inhibit crystallization. The saponification degree can be determined by a method defined in JIS K 6726-1994 “Testing method for polyvinyl alcohol”.

  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.

  Examples of commercially available polyvinyl alcohol resins that can be suitably used are trade names, such as “PVA124” (degree of saponification: 98.0 to 99.0 mol%), “PVA117” (manufactured by Kuraray Co., Ltd.) Saponification degree: 98.0-99.0 mol%), "PVA117H" (saponification degree: 99.5 mol% or more), "PVA624" (saponification degree: 95.0-96.0 mol%) and “PVA617” (degree of saponification: 94.5-95.5 mol%); “AH-26” (degree of saponification: 97.0-98.8 mol%) manufactured by Nippon Synthetic Chemical Industry Co., Ltd. AH-22 "(degree of saponification: 97.5-98.5 mol%)," NH-18 "(degree of saponification: 98.0-99.0 mol%) and" N-300 "(degree of saponification) : 98.0-99.0 mol%); “JC-33” (degree of saponification: manufactured by Nippon Vinegar Poval Co., Ltd.) 9.0 mol% or more), “JM-33” (degree of saponification: 93.5 to 95.5 mol%), “JM-26” (degree of saponification: 95.5 to 97.5 mol%), “JP-45” (degree of saponification: 86.5-89.5 mol%), “JF-17” (degree of saponification: 98.0-99.0 mol%), “JF-17L” (saponification) Degree: 98.0 to 99.0 mol%) and "JF-20" (degree of saponification: 98.0 to 99.0 mol%).

  The coating liquid may contain additives such as a plasticizer and a surfactant as necessary. As the plasticizer, a 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.

(Coating of coating liquid and drying of coating layer)
The above coating solution is applied to the base film by wire bar coating method; roll coating method such as reverse coating and gravure coating; die coating method; comma coating method; lip coating method; spin coating method; A fountain coating method; a dipping method; and a known method such as 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 drying time is, for example, 2 to 20 minutes.

  The polyvinyl alcohol-based resin layer may be formed on only one surface of the base film, or may be formed on both surfaces. When it is formed on both sides, curling of the polarizing laminate film and the film that may occur during the production of the polarizing plate can be suppressed, and two polarizing plates can be obtained from one polarizing laminated film. This is also advantageous.

  The thickness of the polyvinyl alcohol-based resin layer in the laminated film is preferably 3 to 30 μm, and more preferably 5 to 20 μm. If the polyvinyl alcohol-based resin layer 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, which will be described later. A child layer can be obtained. When the thickness of the polyvinyl alcohol-based resin layer exceeds 30 μm, the thickness of the polarizer layer may exceed 10 μm. Moreover, when the thickness of the polyvinyl alcohol-based resin layer is less than 3 μm, the film becomes too thin after stretching and the dyeability tends to deteriorate.

  Prior to coating the coating liquid, in order to improve the adhesion between the base film and the polyvinyl alcohol resin layer, at least the surface of the base film on which the polyvinyl alcohol resin layer is formed is subjected to corona treatment and plasma. You may perform a process, a flame | frame (flame) process, etc.

  Prior to coating the coating liquid, in order to improve the adhesion between the base film and the polyvinyl alcohol resin layer, a polyvinyl alcohol resin layer is formed on the base film via a primer layer or an adhesive layer. It may be formed.

(Primer layer)
The primer layer can be formed by applying a primer layer forming coating solution to the surface of the substrate film 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 and the polyvinyl alcohol-based resin layer. 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.

  Examples of the polyvinyl alcohol resin include polyvinyl alcohol resins and derivatives thereof. Polyvinyl alcohol resin derivatives 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. Among the above-mentioned polyvinyl alcohol resins, it is preferable to use a polyvinyl alcohol resin.

  As the solvent, a general organic solvent or an aqueous solvent capable of dissolving the resin component is usually used. Examples of solvents include, for example, aromatic hydrocarbons such as benzene, toluene and xylene; ketones such as acetone, methyl ethyl ketone and methyl isobutyl ketone; esters such as ethyl acetate and isobutyl acetate; Chlorinated hydrocarbons such as trichlorethylene and chloroform; alcohols such as ethanol, 1-propanol, 2-propanol and 1-butanol. However, if the primer layer is formed using a primer layer forming coating solution containing an organic solvent, the base film may be dissolved, so the solvent should be selected in consideration of the solubility of the base film. Is preferred. In consideration of the influence on the environment, the primer layer is preferably formed 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 used. Examples of the crosslinking agent include epoxy-based, isocyanate-based, dialdehyde-based, and metal-based crosslinking agents.

  As the epoxy-based crosslinking agent, either one-component curable type or two-component curable type can be used. Ethylene glycol diglycidyl ether, polyethylene glycol diglycidyl ether, glycerin di- or tri-glycidyl ether, 1,6-hexane Examples include diol diglycidyl ether, trimethylolpropane triglycidyl ether, diglycidyl aniline, diglycidyl amine and the like.

  Isocyanate-based crosslinking agents include tolylene diisocyanate, hydrogenated tolylene diisocyanate, trimethylolpropane-tolylene diisocyanate adduct, triphenylmethane triisocyanate, methylenebis (4-phenylmethane) triisocyanate, isophorone diisocyanate, and ketoximes thereof. A block thing or a phenol block thing etc. are mentioned.

  Examples of the dialdehyde-based crosslinking agent include glyoxal, malondialdehyde, succindialdehyde, glutardialdehyde, maleidialdehyde, phthaldialdehyde and the like.

  Examples of the metal-based crosslinking agent include metal salts, metal oxides, metal hydroxides, and organometallic compounds. Examples of the metal salt, metal oxide, and metal hydroxide include divalent or higher valent metals such as magnesium, calcium, aluminum, iron, nickel, zirconium, titanium, silicon, boron, zinc, copper, vanadium, chromium, and tin. Examples thereof include salts, oxides and hydroxides of metals having a valence.

  An organometallic compound is a compound having in its molecule at least one structure in which an organic group is bonded directly to a metal atom or an organic group is bonded through an oxygen atom, a nitrogen atom, or the like. The organic group means a monovalent or polyvalent group containing at least a carbon element, and can be, for example, an alkyl group, an alkoxy group, an acyl group, or the like. Further, the bond does not mean only a covalent bond, but may be a coordinate bond by coordination of a chelate compound or the like.

  Suitable examples of the organometallic compound include an organotitanium compound, an organozirconium compound, an organoaluminum compound, and an organosilicon compound. An organometallic compound may be used individually by 1 type, and may use 2 or more types together.

  Examples of the organic titanium compounds include titanium orthoesters such as tetranormal butyl titanate, tetraisopropyl titanate, butyl titanate dimer, tetra (2-ethylhexyl) titanate, tetramethyl titanate; titanium acetylacetonate, titanium tetraacetylacetonate , Titanium chelates such as polytitanium acetylacetonate, titanium octylene glycolate, titanium lactate, titanium triethanolamate, and titanium ethyl acetoacetate; and titanium acylates such as polyhydroxytitanium stearate.

  Examples of the organic zirconium compound include zirconium normal propionate, zirconium normal butyrate, zirconium tetraacetylacetonate, zirconium monoacetylacetonate, zirconium bisacetylacetonate, zirconium acetylacetonate bisethylacetoacetate and the like.

  Examples of the organoaluminum compound include aluminum acetylacetonate and aluminum organic acid chelate. Examples of the organic silicon compound include compounds in which the ligands exemplified above for the organic titanium compound and the organic zirconium compound are bonded to silicon.

  In addition to the above-described low molecular weight crosslinking agents, high molecular weight crosslinking agents such as methylolated melamine resins and polyamide epoxy resins can also be used. Examples of commercially available polyamide epoxy resins include “Smiles Resin 650 (30)” and “Smiles Resin 675” (both trade names) sold by Taoka Chemical Co., Ltd.

  When a polyvinyl alcohol-based resin is used as the resin component forming the primer layer, a polyamide epoxy resin, a methylolated melamine resin, a dialdehyde-based crosslinking agent, a metal chelate compound-based crosslinking agent, or the like is preferably used as the crosslinking agent.

  The ratio of the resin component and the crosslinking agent in the primer layer forming coating solution is from about 0.1 to 100 parts by weight of the crosslinking agent with respect to 100 parts by weight of the resin component. It may be appropriately determined depending on the above, and it is particularly preferable to select from a range of about 0.1 to 50 parts by weight. The primer layer forming coating solution preferably has a solid content concentration of about 1 to 25% by weight.

  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 and the polyvinyl alcohol-based resin layer is small, and when the thickness is more than 1 μm, it is disadvantageous for thinning the polarizing laminated film and the polarizing plate.

  The method for applying the primer layer forming coating solution to the substrate film can be the same as the coating solution for forming the polyvinyl alcohol-based resin layer. The primer layer is applied to the surface (one surface or both surfaces of the base film) on which the coating liquid for forming the polyvinyl alcohol-based resin layer is applied. The drying temperature and drying time of the coating layer comprising the primer layer forming coating solution 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 drying time is, for example, 30 seconds to 20 minutes.

[2] Stretching step S20
This step is a step of obtaining a stretched film by longitudinally uniaxially stretching a laminated film composed of a base film and a polyvinyl alcohol-based resin layer. In this invention, extending | stretching process S20 is divided and performed to the extending | stretching process process of 2 steps | paragraphs or more. That is, the stretching step S20 includes multi-stage stretching, and includes two or more stages of stretching treatment steps. Here, “including two or more steps of stretching treatment” means that the first stage (first) stretching treatment step in which the laminated film is longitudinally uniaxially stretched at a certain draw ratio, and the laminated film is not stretched (in the film transport direction). It means that it has at least a second-stage stretching treatment step in which the laminated film subjected to the first-stage stretching treatment is stretched uniaxially at a certain stretching ratio through a section (time zone) that does not stretch). The stretching step S20 can include three or more steps of stretching treatment. In this case as well, a section (time zone) in which the laminated film is not stretched is interposed between the stretching treatment steps of each step.

  The longitudinal uniaxial stretching in each stage of the stretching treatment step can be, for example, stretching between rolls, rolling, hot roll stretching, stretching using a chuck, or the like. The stretching methods at each stage may all be the same, or different stretching methods may be combined. However, even if the draw ratio is high, if the neck-in rate is low, sufficient polarization performance may not be imparted to the polarizer layer obtained through the dyeing step S30, so that a sufficient neck-in rate is ensured. Therefore, it is preferable that at least one step of the stretching process is performed by stretching between rolls which is free end stretching.

The neck-in rate is expressed by the following formula:
Neck-in rate (%) = [(W1-W2) / W1] × 100
Defined by W1 is the width of the laminated film before being subjected to the stretching step S20. W2 is the minimum width of the film after all stretching processes have been performed on the laminated film. For example, when the stretching process is performed on the laminated film only in the stretching step S20, W2 is the minimum width of the stretched film finally obtained in the stretching step S20. As will be described later, an additional stretching process can also be performed in the dyeing step S30. In this case, W2 is the minimum width of the polarizing laminated film after the additional stretching process. The neck-in rate is preferably about 50% or more.

  Several examples of the multistage stretching in the stretching step S20 will be described with reference to the drawings. In each figure, the arrow means the film transport direction.

  FIG. 2 shows an example in which the stretching step S20 includes a two-stage stretching process, and both of these stretching processes are a roll-to-roll stretching system, that is, a system in which stretching is performed between nip rolls having different peripheral speeds. It is. Specifically, the conveyed laminated film 10 is first stretched between the nip roll 1 and the nip roll 2 having different peripheral speeds while being heated by passing through the heating furnace 20 set to a desired temperature ( First stage stretching process). The first-stage stretched film is further conveyed by the guide roll 5 and heated by passing through the heating furnace 30 set to a desired temperature, while the nip roll 3 and the nip roll 4 having different peripheral speeds are mutually connected. Is stretched (second-stage stretching process) to become a stretched film 15. Since the peripheral speed of the nip roll 2 and the peripheral speed of the nip roll 3 are the same in the section from the nip roll 2 to the nip roll 3, the film is not stretched.

  FIG. 3 shows an example in which the stretching step S20 includes a three-stage stretching process, and each of these stretching processes is a hot roll stretching method, that is, a method of stretching between heated rolls. It is. Specifically, the transported laminated film 10 is first stretched while the surface is adjusted to a desired temperature and passes between the hot rolls 6 to 7 having different peripheral speeds (first-stage stretching). Processing step). Next, the surface is adjusted to a desired temperature through a section where no stretching occurs, that is, a section in contact with the heat roll 7, and the surface is stretched while passing between the heat roll 7 and the heat roll 8 having different peripheral speeds. (Second-stage stretching process). The film subjected to the second-stage stretching treatment has a section in which stretching does not occur, that is, a section in contact with the heat roll 8, the surface is adjusted to a desired temperature, and the heat roll 8-heat having different peripheral speeds. The film is stretched while passing between the rolls 9 (third-stage stretching treatment step) to form a stretched film 15. .

  FIG. 4 is a schematic diagram for explaining a longitudinal uniaxial stretching method using a chuck (clip), and is a view when a laminated film to be stretched is viewed from above. In the longitudinal uniaxial stretching method using a chuck, as shown in the drawing, a plurality of chucks 40 are attached to both ends of the laminated film 10 in the width direction (usually at regular intervals), and the laminated film 10 heated to a desired temperature is attached. A method of stretching by gradually increasing the inter-chuck distance R in the film transport direction while transporting. Although not shown, in order to perform multi-stage stretching by a longitudinal uniaxial stretching method using a chuck, the inter-chuck distance R is widened and the stretching process (first stretching process step) is performed, and then the inter-chuck distance R is fixed. After passing through the section in which the laminated film 10 is conveyed, the inter-chuck distance R may be increased again to perform the stretching process (second-stage stretching process). The same applies to the third and subsequent steps.

  The method for controlling the inter-chuck distance R during stretching is not particularly limited, and various methods can be used. For example, each chuck can be driven independently, and each chuck may be controlled independently to control the distance R between chucks, or the chucks are connected to each other. The chuck distance may be controlled to control the inter-chuck distance R. Any method can be suitably used in the present invention.

  Specific methods for independently driving individual chucks include a method using magnetic force as typified by a linear motor drive system, a method of attaching a rotary drive motor or the like to each chuck, and the like. Instead of independently driving all the chucks, only a part of the chucks can be independently driven, and the other remaining chucks can be controlled not to be specially controlled.

  As a specific method for controlling a plurality of chucks with one drive system, a pantograph method or the like is typical. The pantograph system is a system that controls the distance R between chucks by opening and closing the pantograph by controlling the distance between two rails.

  None of the above-described multistage stretching illustrated with reference to FIGS. 2 to 4 is accompanied by film winding / unwinding for each stretching process. Such an embodiment is preferable in terms of productivity. However, the present invention is not limited to the above example, and the film may be wound up every time one step of the stretching process is completed, and unwound again when the next stretching process is performed.

  In the present invention, the ratio of the draw ratio in the first drawing process to the draw ratio in the second drawing process (hereinafter also referred to as “stretch ratio”) is 0.5 or more. “The draw ratio in the first stretching step” means that the length in the longitudinal direction (stretched direction) of the polyvinyl alcohol-based resin layer of the laminated film before being subjected to the stretching step S20 is 1. It is the length of the longitudinal direction of the polyvinyl alcohol-type resin layer at the time of completion | finish of the extending | stretching process of the 1st step | paragraph. For example, the length in the longitudinal direction of the polyvinyl alcohol-based resin layer (or the length of the portion having the polyvinyl alcohol-based resin layer) of the laminated film before being subjected to the stretching step S20 is 1, and the first-stage stretching treatment When the length of the polyvinyl alcohol-based resin layer (or the length of the certain portion) is 2 by the process, the stretch ratio in the first stretching process is doubled.

  The “stretch ratio in the second stage stretching process” is the second stage stretching process when the length in the longitudinal direction of the polyvinyl alcohol-based resin layer at the end of the first stage stretching process is 1. It is the length of the longitudinal direction of the polyvinyl alcohol-type resin layer at the time of completion | finish.

  The stretching film S20 is divided into two or more stretching process steps, and the first and second stretching process steps are performed so as to satisfy the above-described stretching ratio, thereby obtaining a laminated film up to a desired total stretching ratio. In the process of stretching the film, it becomes possible to stretch the laminated film while maintaining the neck-in due to stretching at an appropriate level, so that the generation of wrinkles during stretching can be effectively suppressed, and the film width Stretching unevenness (non-uniform stretching) in the direction can be effectively suppressed.

  The generation of wrinkles not only can cause uneven dyeing in the dyeing step S30, and thus poor appearance, optical properties such as polarization performance and transmittance, and can cause a decrease in yield. Stretch unevenness appears as thickness unevenness in the film width direction, and can similarly cause unevenness in optical properties such as polarization performance and transmittance.

  According to the method of the present invention, a stretched film having a thickness difference in the film width direction of less than 5 μm and further less than 4 μm can be produced, and thus a polarizing laminated film and a polarizing plate having uniform polarization performance and transmittance are produced. can do. “Thickness difference in the film width direction” means that the film thickness is measured at one point at a position of 50 mm from one end in the film width direction, and the film thickness at the center position in the film width direction is measured at one point. It means the absolute value of the difference in thickness.

  The draw ratio is preferably 0.6 or more, more preferably 0.7 or more, in order to obtain the above-described effects more effectively. When the draw ratio is less than 0.5, uneven drawing in the film width direction occurs. Moreover, since wrinkles are likely to occur when the stretch ratio is too large, the stretch ratio is preferably 5 or less, and more preferably 4 or less.

  The draw ratio in the first drawing step is preferably less than 5 times, more preferably 4 times or less. Wrinkles tend to occur when the draw ratio is 5 times or more. That is, in order to impart good polarization performance to the polarizer layer obtained through the dyeing step S30, it is desirable that the total stretching ratio of the stretching treatment performed on the laminated film is 5 times or more as described later. When such a high-magnification stretching process is performed in one stage, wrinkles are generated. In the present invention, the stretching process is performed in two or more stages in consideration of the above.

  The above-mentioned “total stretching ratio” means each stage of the stretching process (as will be described later, an additional stretching process can also be performed in the dyeing process S30. In this case, the additional stretching process is included. ) Means the final draw ratio multiplied by the draw ratio, in other words, the longitudinal direction (stretched direction) of the polyvinyl alcohol-based resin layer of the laminated film before being subjected to the stretching step S20. Is the length in the longitudinal direction of the polyvinyl alcohol-based resin layer at the end of all stretching treatments, that is, the polarizer layer.

  As described above, the total draw ratio of the polarizer layer is preferably more than 5 times based on the polyvinyl alcohol resin layer of the laminated film. When the draw ratio is 5 times or less, the polyvinyl alcohol-based resin layer is not sufficiently oriented, and thus the degree of polarization of the polarizer layer tends not to be sufficiently high. The total draw ratio is preferably 8 times or less. When the total draw ratio exceeds 8 times, the film is likely to be broken during stretching, and the thickness of the stretched film becomes unnecessarily thin, and the workability and handleability in subsequent processes may be reduced.

  The stretching temperature in each stage of the stretching step S20 is set to be higher than the temperature at which the polyvinyl alcohol-based resin layer and the entire base film can be stretched, and preferably has a melting point of −30 ° C. to +30 of the base film. It is in the range of ° 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 is composed of a plurality of resin layers, the melting point means the highest melting point among melting points of the plurality of resin layers.

  If the stretching temperature is lower than the melting point of the base film of −30 ° C., the fluidity of the base film tends to be too low to make the stretching process difficult. When the stretching temperature exceeds + 30 ° C. of the melting point, the fluidity of the base film is too high and the stretching treatment tends to be difficult as well. In view of the ease of the stretching treatment, the stretching temperature is within the above range, and more preferably 120 ° C. or higher.

  As a heating method of the laminated film in each stage of the stretching treatment, a zone heating method (for example, a method of heating in a stretching zone such as a heating furnace in which hot air is blown and adjusted to a predetermined temperature; see FIG. 2); In the case of using and stretching, there are a method of heating the roll itself (see FIG. 3); a heater heating method (a method in which infrared heaters, halogen heaters, panel heaters and the like are installed above and below the laminated film 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. In this case, the two nip roll pairs may be installed in the temperature-controlled stretching zone or outside the stretching zone, but are installed outside the stretching zone to prevent adhesion between the laminated film and the nip roll. Is preferred (see FIG. 2).

  The stretching temperature means the atmospheric temperature in the zone (for example, in the heating furnace) in the case of the zone heating method, and also means the atmospheric temperature in the furnace in the case of heating in the furnace even in the heater heating method. Moreover, in the case of the method of heating roll itself, the surface temperature of a roll is meant.

  Prior to the stretching step S20, a preheat treatment step for preheating the laminated film may be provided. As the preheating method, the same method as the heating method in the stretching process can be used. When the stretching method is inter-roll stretching, preheating may be performed at any timing before passing through the upstream nip roll, during passing, or after passing. When the stretching method is hot roll stretching, preheating is preferably performed at a timing before passing through the hot roll. When the stretching method is stretching using a chuck, preheating is preferably performed at a timing before increasing the distance between chucks. 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 of the last stage in extending process S20. The heat setting process is a process of performing a heat treatment at a temperature equal to or higher than the crystallization temperature while maintaining the tensioned state with the end of the stretched film held by a clip. By this heat setting treatment, crystallization of the polyvinyl alcohol-based resin layer is promoted. 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
In this step, the polyvinyl alcohol-based resin layer of the stretched film is dyed with a dichroic dye and adsorbed and oriented to form a polarizer layer. Through this step, a polarizing laminated film in which a polarizer layer is laminated on one side or both sides of a base film is obtained.

  Specific examples of the dichroic dye include iodine and dichroic organic dyes. Specific examples of the dichroic organic dye include, for example, Red BR, Red LR, Red R, Pink LB, Rubin BL, Bordeaux GS, Sky Blue LG, Lemon Yellow, Blue BR, Blue 2R, Navy RY, Green LG, Violet LB, Violet B, Black H, Black B, Black GSP, Yellow 3G, Yellow R, Orange LR, Orange 3R, Scarlet GL, Scarlet KGL, Congo Red, Brilliant Violet BK, Splat Blue G, Splat Blue GL, Splat Orange GL , Direct Sky Blue, Direct First Orange S, First Black, etc. A dichroic dye may be used individually by 1 type, and may use 2 or more types together.

  The dyeing step can be performed by immersing the entire stretched film 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 immersion time of the stretched film in the dyeing solution is usually in the range of 15 seconds to 15 minutes, preferably 30 seconds to 3 minutes. Moreover, it is preferable that it is in the range of 10-60 degreeC, and, as for the temperature of a dyeing | staining solution, it is more preferable that it exists in the range of 20-40 degreeC.

  In addition, you may perform a extending | stretching process further with respect to a stretched film during dyeing process S30. Embodiments in this case are as follows: 1) In the stretching step S20, after the stretching process is performed at a lower ratio than the target, the stretching process is performed so that the total stretching ratio becomes the target ratio during the dyeing process in the dyeing process S30. In the case of performing the crosslinking treatment after the dyeing treatment, as described later, 2) In the drawing step S20, after the drawing treatment at a lower magnification than the target in the drawing step S20, 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 total stretching ratio does not reach the target ratio, and then the stretching process is performed during the crosslinking process so that the final total stretching ratio becomes the 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 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 immersion time of the dyed film in the crosslinking solution is usually 15 seconds to 20 minutes, and preferably 30 seconds to 15 minutes. Moreover, it is preferable that the temperature of a crosslinking solution exists in the range of 10-90 degreeC.

  In addition, a crosslinking process can also be performed simultaneously with a dyeing | staining process by mix | blending a crosslinking agent in a 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.

  It is preferable to perform a washing | cleaning process and a drying process after dyeing process S30 and before 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 immersion time in water is usually 2 to 300 seconds, preferably 3 to 240 seconds.

  The washing step may be a combination of a water washing step and a washing step with an iodide solution. In addition to water, liquids such as methanol, ethanol, isopropyl alcohol, butanol, and propanol can be appropriately contained in the cleaning liquid used in the water cleaning step and / or the cleaning process using the iodide solution.

  As a drying process performed after the washing process, any appropriate method such as natural drying, air drying, and heat drying can be adopted. For example, in the case of heat drying, the drying temperature is usually 20 to 95 ° C., and the drying time is usually about 1 to 15 minutes. The polarizing laminated film obtained as described above can be used as a polarizing element as it is, and is also useful as an intermediate for producing a polarizing plate comprising a polarizer layer and a protective film.

  The thickness of the polarizer layer of the polarizing laminate film is 10 μm or less, preferably 7 μm or less. By setting the thickness of the polarizer layer to 10 μm or less, a thin polarizing laminated film can be formed.

<Production method of polarizing plate>
The manufacturing method of the polarizing plate of this invention is the process of preparing the above-mentioned polarizing laminated film, bonding process S40 which bonds a protective film on the polarizer layer of a polarizing laminated film, and obtains a bonding film, bonding The peeling process S50 which peels and removes the base film from the film is included in this order.

[4] Pasting step S40
This step is a step of obtaining a bonding film by bonding a protective film on the polarizer layer of the polarizing laminated film, that is, on the surface opposite to the substrate film side of the polarizer layer. The protective film can be bonded to the polarizer layer using an adhesive or a pressure-sensitive adhesive. When a polarizing laminated film has a polarizer layer on both surfaces of a base film, a protective film is normally bonded on the polarizer layers on both surfaces. In this case, these protective films may be the same type of protective film or different types of protective films.

(Protective film)
The protective film is, for example, a polyolefin resin such as a chain polyolefin resin (such as a polypropylene resin) or a cyclic polyolefin resin (such as a norbornene resin); a cellulose ester resin such as cellulose triacetate or cellulose diacetate; The film may be a polyester resin such as terephthalate, polyethylene naphthalate, or polybutylene terephthalate; a polycarbonate resin; a (meth) acrylic resin; or a mixture or copolymer thereof. Examples of commercially available products such as cyclic polyolefin resins and films thereof, and cellulose triacetate are as described above.

  The protective film 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 resin film made of the above material (uniaxial stretching or biaxial stretching, etc.) or forming a liquid crystal layer or the like on the film. can do.

  An optical layer such as a hard coat layer, an antiglare layer, or an antireflection layer can be formed on the surface of the protective film opposite to the polarizer layer. The method for forming these optical layers on the surface of the protective film is not particularly limited, and a known method can be used. The optical layer may be formed in advance on the protective film prior to the bonding step S40, or may be formed after the bonding step S40 or after the peeling step S50 described later.

  When bonding a protective film on the polarizer layer, plasma treatment, corona treatment, ultraviolet irradiation treatment, flame (flame) is applied to the surface of the protective film on the polarizer layer side in order to improve adhesion to the polarizer layer. ) Surface treatment (easily adhesion treatment) such as saponification treatment, plasma treatment, corona treatment or saponification treatment is preferred. For example, when the protective film is made of a cyclic polyolefin-based 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.

  The thickness of the protective film is preferably thin, but if it is too thin, the strength is lowered and the processability is poor. On the other hand, when too thick, problems, such as transparency falling and the curing time required after bonding, will arise. Therefore, the thickness of the protective film is preferably 90 μm or less, more preferably 5 to 60 μm, and still more preferably 5 to 50 μm. From the viewpoint of thinning the polarizing plate, the total thickness of the polarizer layer and the protective film is preferably 100 μm or less, more preferably 90 μm or less, and further preferably 80 μm or less.

(adhesive)
As the adhesive, 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 and a water-based two-component urethane emulsion adhesive. In particular, when a cellulose ester resin film that has been surface-treated (hydrophilized) by a saponification treatment or the like is used as a protective film, it is preferable to use a water-based adhesive composed of an aqueous polyvinyl alcohol resin 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 a polymer or a modified polyvinyl alcohol polymer obtained by partially modifying a hydroxyl group thereof can be used. The water-based adhesive can include additives such as polyvalent aldehydes, water-soluble epoxy compounds, melamine compounds, zirconia compounds, and zinc compounds. When an aqueous adhesive is used, the thickness of the adhesive layer obtained therefrom is usually 1 μm or less.

  A water-based adhesive is applied on the polarizer layer and / or protective film of the polarizing laminated film, and these films are bonded via the adhesive layer, preferably pressed and bonded using a bonding roll or the like. A pasting process is carried out by making it. 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. When it is lower than 30 ° C., the protective film tends to be peeled off from the polarizer layer. If the drying temperature exceeds 90 ° C., the polarizing performance of the polarizer layer 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 cures when irradiated with active energy rays such as ultraviolet rays. For example, an adhesive containing a polymerizable compound and a photopolymerization initiator, an adhesive containing a photoreactive resin, and a binder. The thing containing resin and a photoreactive crosslinking agent 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 active energy rays, such as 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 performing the above-mentioned pasting, a drying process is performed as necessary (such as when the photocurable adhesive contains a solvent), and then light is irradiated by activating active energy rays. A curing step for curing the curable adhesive is performed. The light source of the active energy ray is not particularly limited, but an active energy ray having a light emission distribution at a wavelength of 400 nm or less is preferable, and specifically, 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 microwave excitation mercury lamp, a metal halide lamp and the like are preferably used.

The light irradiation intensity to the photocurable adhesive is appropriately determined depending on the composition of the photocurable adhesive, and the irradiation intensity in the wavelength region effective for activating the polymerization initiator is 0.1 to 6000 mW / cm ^2. It is preferable to set to. When the irradiation intensity is 0.1 mW / cm ² or more, the reaction time does not become too long, and when the irradiation intensity is 6000 mW / cm ² or less, the light emitted from the light source and the light generated by the curing of the photocurable adhesive There is little risk of yellowing of the curable adhesive and deterioration of the polarizer layer.

The light irradiation time for the photocurable adhesive is also determined appropriately depending on the composition of the photocurable adhesive, and the integrated light amount expressed as the product of the irradiation intensity and the irradiation time is 10 to 10,000 mJ / cm ^2. It is preferable to set to. When the integrated light amount is 10 mJ / cm ² or more, a sufficient amount of active species derived from the polymerization initiator can be generated to advance the curing reaction more reliably, and when it is 10000 mJ / cm ² or less, the irradiation time is long. It does not become too much, and good productivity can be maintained.

  In addition, the thickness of the adhesive bond layer after active energy ray irradiation is about 0.001-5 micrometers normally, Preferably it is 0.01-2 micrometers, More preferably, it is 0.01-1 micrometer.

(Adhesive)
The pressure-sensitive adhesive that can be used for bonding the protective film is usually based on an 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. It consists of the added adhesive composition. Furthermore, it can also be set as the adhesive layer which contains microparticles | fine-particles and shows light-scattering property.

  Although the thickness of the pressure-sensitive adhesive layer can be 1 to 40 μm, it is preferably applied thinly, as long as it does not impair the workability and durability characteristics, and specifically 3 to 25 μm. A thickness of 3 to 25 μm has good processability and is suitable for suppressing dimensional changes of the polarizer layer. When the pressure-sensitive adhesive layer is less than 1 μm, the tackiness is lowered, and when it exceeds 40 μm, problems such as the pressure-sensitive adhesive protruding easily occur. In the method of bonding the protective film to the polarizer layer using the pressure-sensitive adhesive, after the pressure-sensitive adhesive layer is provided on the protective film surface, it may be bonded to the polarizer layer, or the pressure-sensitive adhesive layer on the surface of the polarizer layer. After providing, you may paste a protective film here.

  The method for forming the pressure-sensitive adhesive layer is not particularly limited, and a pressure-sensitive adhesive composition (pressure-sensitive adhesive solution) containing each component including the above-mentioned base polymer is applied to the protective film surface or the polarizer layer surface. After drying and forming the pressure-sensitive adhesive layer, the protective film and the polarizer layer may be bonded together, or after forming the pressure-sensitive adhesive layer on the separator (release film), the pressure-sensitive adhesive layer is applied to the surface of the protective film. Or you may make it transfer on a polarizing film surface and then bond a protective film and a polarizer layer together. When the pressure-sensitive adhesive layer is formed on the protective film surface or the polarizer layer surface, surface treatment such as corona treatment is applied to the protective film surface or the polarizing polarizer layer surface, or one or both surfaces of the pressure-sensitive adhesive layer as necessary. Also good.

[5] Peeling step S50
This process is a peeling removal process of a base film from the bonding film obtained by bonding a protective film. Through this step, a polarizing plate in which a protective film is laminated on the polarizer layer can be obtained. When the polarizing laminated film has a polarizer layer on both sides of the base film, and a protective film is bonded to both of these polarizer layers, this peeling step S50 allows the two polarizing laminate films to be removed. A sheet of polarizing plate is obtained.

  The method of peeling and removing the base film is not particularly limited, and the peeling can be performed by the same method as the separator (peeling film) peeling step performed by a normal pressure-sensitive adhesive polarizing plate. After the bonding step S40, the base film may be peeled off as it is, or after the bonding step S40, it may be wound up into a roll and peeled off in the subsequent step.

  The polarizing plate produced as described above can be used as an optical film in which other optical layers are laminated in practical use. Moreover, the protective film may have the function of such an optical layer. As another optical layer, a reflective polarizing film that transmits a certain kind of polarized light and reflects polarized light having the opposite properties; a film with an antiglare function having an uneven shape on the surface; a film with a surface antireflection function A reflective film having a reflective function on the surface; a transflective film having both a reflective function and a transmissive function; and a viewing angle compensation film.

  For example, “DBEF” (manufactured by 3M, Sumitomo 3M Co., Ltd. in Japan) can be used as a commercial product corresponding to a reflective polarizing film that transmits certain types of polarized light and reflects polarized light that exhibits the opposite properties. Available), “APF” (manufactured by 3M, available from Sumitomo 3M Limited in Japan).

  Examples of the viewing angle compensation film include an optical compensation film in which a liquid crystal compound is applied to the substrate surface, and is oriented / fixed, a retardation film made of a polycarbonate resin, a retardation film made of a cyclic polyolefin resin, and the like. .

  Commercially available products corresponding to the optical compensation film in which a liquid crystal compound is applied to the substrate surface and aligned and fixed are “WV film” (manufactured by Fujifilm Corporation), “NH film” (JX Nippon Mining & Metals). Energy Co., Ltd.), “NR Film” (manufactured by JX Nippon Oil & Energy Corporation), and the like.

  Commercial products corresponding to retardation films made of cyclic polyolefin resins include “Arton Film” (manufactured by JSR Corporation), “Essina” (manufactured by Sekisui Chemical Co., Ltd.), “Zeonor Film” (Nippon Zeon ( Etc.).

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

<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 long base film having a three-layer structure in which a resin layer composed of a propylene homopolymer (“Sumitomo Noblen FLX80E4” manufactured by Sumitomo Chemical Co., Ltd., melting point Tm = 163 ° C.) is disposed on a multilayer extruder It was produced by the coextrusion molding used. The total thickness of the base film was 100 μm, and the thickness ratio (FLX80E4 / W151 / FLX80E4) of each layer was 3/4/3.

(2) Production of laminated film (resin layer forming step)
Polyvinyl alcohol powder (“Z-200” manufactured by Nippon Synthetic Chemical Industry Co., Ltd., average polymerization degree 1100, average saponification degree 99.5 mol%) was dissolved in hot water at 95 ° C. An aqueous alcohol solution was prepared. The resulting aqueous solution was mixed with a crosslinking agent (“Smiles Resin 650” manufactured by Taoka Chemical Industry Co., Ltd.) at a ratio of 1 part by weight with respect to 2 parts by weight of the polyvinyl alcohol powder to form a primer layer forming coating solution. Got.

  Polyvinyl alcohol powder ("PVA124" manufactured by Kuraray Co., Ltd., average polymerization degree 2400, average saponification degree 98.0-99.0 mol%) was dissolved in hot water at 95 ° C, and the concentration was 8% by weight. A polyvinyl alcohol aqueous solution was prepared and used as a coating liquid for forming a polyvinyl alcohol-based resin layer.

  While continuously transporting the base film produced in (1) above, corona treatment is performed on one side, and the primer layer forming coating solution is continuously applied to the corona-treated surface using a micro gravure coater. And a primer layer having a thickness of 0.2 μm was formed by drying at 80 ° C. for 3 minutes. Subsequently, the polyvinyl alcohol-based resin layer-forming coating solution was continuously applied onto the primer layer using a comma coater while transporting the film, and the coating liquid for forming the polyvinyl alcohol-based resin layer was 90 ° C. for 1 minute, 70 ° C. for 3 minutes, and then 60 A polyvinyl alcohol resin layer having a thickness of 10.0 μm was formed on the primer layer by drying at 4 ° C. for 4 minutes.

  Furthermore, the base film surface opposite to the surface on which the polyvinyl alcohol-based resin layer is formed is treated in the same manner as described above, and a primer layer and a polyvinyl alcohol-based resin layer are sequentially formed on both surfaces of the base film. A laminated film comprising a primer layer having a thickness of 0.2 μm and a polyvinyl alcohol resin layer having a thickness of 10.0 μm, and comprising a layer structure of polyvinyl alcohol resin layer / primer layer / base film / primer layer / polyvinyl alcohol resin layer. Got.

(3) Production of stretched film (stretching process)
While continuously transporting the laminated film produced in (2) above using the stretching apparatus shown in FIG. 2, a two-stage longitudinal uniaxial stretching process (free-end uniaxial stretching in the film transport direction) by a nip roll stretching method. ) To prepare a stretched film. The stretching temperature (atmospheric temperature in the heating furnaces 20 and 30) in the two-stage stretching process was 160 ° C. The draw ratios in the first and second steps were adjusted to 2.00 times and 2.90 times by adjusting the peripheral speeds of the nip rolls 1, 2, 3, and 4, respectively. The total draw ratio is 5.80 times. As for the thickness of the polyvinyl alcohol-type resin layer in a stretched film, one side was 4.6 micrometers and the other was 4.8 micrometers.

  The resulting stretched film was not wrinkled by stretching. When the thickness difference in the film width direction defined above was measured for the obtained stretched film, it was 3 μm, and it was confirmed that the film was stretched with a substantially uniform thickness distribution in the film width direction.

(4) Production of polarizing laminated film (dyeing process)
While continuously stretching the stretched film prepared in (3) above, dipping it in a 60 ° C. warm water bath so that the residence time is 60 seconds, and then in a dyeing solution at 30 ° C. containing iodine and potassium iodide. The polyvinyl alcohol resin layer was dyed by dipping so that the residence time was about 150 seconds, and then the excess dyeing solution was washed away with pure water at 10 ° C. Subsequently, a crosslinking treatment was performed by dipping in a crosslinking solution at 76 ° C. containing boric acid and potassium iodide so that the residence time was 600 seconds. Thereafter, the film was washed with pure water at 10 ° C. for 4 seconds and dried at 80 ° C. for 300 seconds to prepare a polarizing laminated film.

(5) Preparation of polarizing plate (bonding process and peeling process)
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, while continuously transporting the polarizing laminated film prepared in (4) above, the adhesive aqueous solution was coated on the polarizer layers on both sides, and then the saponification treatment was performed on the bonding surface. By laminating a film [transparent protective film made of triacetylcellulose (TAC) (“KC4UY” manufactured by Konica Minolta Opto Co., Ltd.), thickness 40 μm] on the polarizer layer and passing between a pair of laminating rolls It bonded and produced the bonding film which consists of a layer structure of TAC / polarizer layer / primer layer / base film / primer layer / polarizer layer / TAC (bonding process).

  Next, the base film is peeled and removed from the laminated film, and is composed of TAC / polarizer layer / primer layer. Two transparent protective films made of TAC are laminated on the polarizer layer via an adhesive layer. A polarizing plate was obtained. In the process of peeling the above base film, problems such as breakage did not occur.

<Example 2>
A polarizing plate was produced in the same manner as in Example 1 except that the stretching ratios in the first and second stretching processes were 2.50 times and 2.32 times (total stretching ratio 5.80 times), respectively. did. As for the thickness of the polyvinyl alcohol-type resin layer in a stretched film, one was 4.8 micrometers and the other was 5.0 micrometers. No wrinkles were observed in the stretched film, the thickness difference in the film width direction was 2 μm, and the stretching was performed uniformly. The pasting step and the peeling step proceeded without any problem, and a polarizing plate on which a protective film was laminated could be obtained.

<Example 3>
A polarizing plate was produced in the same manner as in Example 1 except that the stretching ratios in the first and second stretching processes were 2.80 times and 2.07 times (total stretching ratio 5.80 times), respectively. did. As for the thickness of the polyvinyl alcohol-type resin layer in a stretched film, one side was 5.2 micrometers and the other was 5.4 micrometers. No wrinkles were observed in the stretched film, the thickness difference in the film width direction was 2 μm, and the stretching was performed uniformly. The pasting step and the peeling step proceeded without any problem, and a polarizing plate on which a protective film was laminated could be obtained.

<Example 4>
A polarizing plate was produced in the same manner as in Example 1 except that the stretching ratios in the first and second stretching processes were 3.40 times and 1.70 times (total stretching ratio 5.78 times), respectively. did. As for the thickness of the polyvinyl alcohol-type resin layer in a stretched film, one side was 5.1 micrometers and the other was 5.3 micrometers. No wrinkles were observed in the stretched film, the thickness difference in the film width direction was 2 μm, and the stretching was performed uniformly. The pasting step and the peeling step proceeded without any problem, and a polarizing plate on which a protective film was laminated could be obtained.

<Comparative Example 1>
A stretched film was produced in the same manner as in Example 1 except that the stretching ratio in the first-stage stretching treatment was 5.80 times and the second-stage stretching treatment was not performed. In the obtained stretched film, strong wrinkles were generated in the stretching direction.

<Comparative example 2>
A stretched film is produced in the same manner as in Example 1 except that the stretching ratio in the first and second stretching processes is 1.54 times and 3.80 times (total stretching ratio 5.85 times), respectively. did. As for the thickness of the polyvinyl alcohol-type resin layer in a stretched film, one side was 4.7 micrometers and the other was 5.2 micrometers. Although no wrinkles were observed in the obtained stretched film, the thickness difference in the film width direction was as large as 7 μm, and the stretching was not uniform.

  Stretch ratio in the first stage and second stage stretch processes, ratio of stretch ratio (ratio of stretch ratio in the first stage stretch process with respect to stretch ratio in the second stage stretch process), total stretch ratio, and stretch Table 1 summarizes the measurement results of wrinkles and thickness differences in the film width direction.

  1, 2, 3, 4 Nip roll, 5 guide roll, 6, 7, 8, 9 heat roll, 10 laminated film, 15 stretched film, 20, 30 heating furnace, 40 chuck.

Claims (6)

After applying a coating liquid containing a polyvinyl alcohol-based resin on at least one surface of the base film, a resin layer forming step of obtaining a laminated film by forming a polyvinyl alcohol-based resin layer by drying,
Stretching process for obtaining a stretched film by longitudinally uniaxially stretching the laminated film,
A dyeing 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;
The stretching step includes two or more stretching treatment steps,
The ratio of the stretching ratio in the first stretching process to the stretching ratio in the second stretching process is 0.5 or more,
The method for producing a polarizing laminated film, wherein the total draw ratio of the polarizer layer is more than 5 times based on the polyvinyl alcohol resin layer of the laminated film.   The manufacturing method of the light-polarizing laminated film of Claim 1 which forms the said polyvinyl alcohol-type resin layer on both surfaces of the said base film in the said resin layer formation process.   The method for producing a polarizing laminated film according to claim 1 or 2, wherein a thickness of the polyvinyl alcohol-based resin layer of the laminated film is 3 to 30 µm.   The method for producing a polarizing laminated film according to any one of claims 1 to 3, wherein a draw ratio in the first drawing step is less than 5.   The said base film consists of polypropylene resin, The manufacturing method of the light-polarizing laminated film in any one of Claims 1-4. Preparing a polarizing laminated film obtained by the production method according to claim 1;
A step of bonding a protective film on the polarizer layer of the polarizing laminate film to obtain a bonding film;
A step of peeling the base film from the bonding film;
The manufacturing method of a polarizing plate provided with.

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