TWI522246B - Polyester film for polarizer protection, polarizing plate and liquid crystal display device - Google Patents

Description

Polyester film for polarizer protection, polarizing plate and liquid crystal display device

The present invention relates to a polyester film for protecting a polarizer used for protecting a polarizer. In particular, it is a polyester film for polarizer protection which is high in transmittance and excellent in adhesion to a polarizer.

In the liquid crystal display device, the polarizing plate is disposed on both sides of the glass substrate on the surface of the liquid crystal panel due to the image forming method. In general, the polarizing plate has a configuration in which a polarizing film comprising a polyvinyl alcohol-based film and a dichroic material such as iodine is bonded to a polarizing film such as a polyvinyl alcohol-based resin to adhere to a polarizing film. Sheet protective film. As a protective film for protection of a polarizer, a triethylenesulfonated cellulose film has been conventionally used from the viewpoint of optical properties or transparency.

However, the durability of triethyl fluorenyl cellulose is insufficient. If a polarizing plate using a triethylene fluorene-based cellulose film as a polarizer protective film is used under high temperature or high humidity, the polarizing property and the color-equal performance of the polarizing plate may be obtained. Low situation. In addition, in order to reduce the thickness of the display in recent years, thin film formation of the polarizing plate has been sought. However, from the viewpoint of maintaining moisture barrier properties, the film formation of the triacetyl cellulose film has its limit. Therefore, it has been proposed to use a polyester film as a polarizer protective film having durability and moisture barrier properties (see Patent Documents 1 to 5).

Triethylenesulfonyl cellulose used as a polarizer protective film The film is subjected to alkali treatment or the like on the surface, and has a very high affinity with a hydrophilic adhesive. Therefore, the protective film composed of the triethylenesulfonated cellulose film has extremely high adhesion to the polarizer coated with the hydrophilic adhesive. However, the polyester film is insufficient in adhesion to a hydrophilic adhesive, and in particular, a polyester film having an alignment property by stretching treatment is more remarkable. Then, in Patent Documents 1 to 3 and 5, it is proposed to provide an easy-adhesion layer on the polyester film in order to improve the adhesion to the polarizer or the hydrophilic adhesive applied to the polarizer.

[Previous Technical Literature] [Patent Literature]

[Patent Document 1] Japanese Patent Laid-Open No. Hei 8-271733

[Patent Document 2] Japanese Patent Laid-Open No. Hei 8-271734

[Patent Document 3] Japanese Patent Laid-Open Publication No. 2009-157361

[Patent Document 4] Japanese Patent Laid-Open Publication No. 2010-277028

[Patent Document 5] Japanese Patent Laid-Open Publication No. 2011-8170

The tendency of the polyester film to have a low affinity for water and a polyester film having an aromatic dicarboxylic acid as a dicarboxylic acid component is particularly remarkable. Further, the polyester film having crystal orientation by stretching has a lower affinity with water. On the other hand, the polarizer or the adhesive applied to the polarizer is mainly composed of a polyvinyl alcohol-based resin and has high hydrophilicity. Due to such a difference in properties, the affinity between the polyester film and the polarizer or the adhesive is low, and it is difficult to firmly follow the two. So even the patent literature The polyester film having an easy-to-attach layer disclosed in 1 to 3 and 5 has not obtained sufficient adhesion as compared with the triethylenesulfonated cellulose film. Therefore, when a polarizing plate using a conventional polyester film as a protective film is used as a display member for a long period of time, floating or peeling occurs between the protective film/polarizer, and the moisture content in the polarizer changes. There is a case where the visibility is deteriorated, and visibility such as whitening is deteriorated.

Moreover, compared with the triethylenesulfonated cellulose film which is generally used as a polarizer protective film, a polarizing plate which uses a polyester film as a polarizer protective film is because the refractive index of the polyester film is higher than that of the trimethyl fluorene group. The cellulose film has a problem that light scattering due to surface reflection is large and the transmittance is lowered.

In view of the above, an object of the present invention is to provide a polyester film for protecting a polarizer, which is provided with a polyvinyl alcohol-based resin layer such as a polyester film and a polarizer or an adhesive applied to the polarizer. The member has a high transmittance of light.

In order to solve the above problems, the inventors of the present invention have tried to solve the above problems, and have conceived that a polyester resin having a high affinity with a polyester film and a polyester film and a polyvinyl alcohol-based resin layer are provided. A layer of a polyvinyl alcohol-based resin having high affinity with a polyvinyl alcohol-based resin layer and a crosslinking agent. However, the inventors of the present invention have found that the mere combination of the polyester film and the polyvinyl alcohol-based resin layer by the respective components cannot be sufficiently exhibited by simply combining these components. Then, as a result of repeated research conducted by the inventors of the present invention, it has been found that, in the above concept, a polyester resin having a certain acid value is used as the polyester resin, and By using a polyvinyl alcohol-based resin having a certain degree of saponification as the polyvinyl alcohol-based resin, it is possible to effectively exhibit the function of each of the components and the resin layer having high affinity.

As a result of further investigations based on the above findings, the inventors of the present invention have found that a polyester film and a polyvinyl alcohol-based resin layer such as a polarizer or an adhesive can be made stronger by using a crosslinking agent having high reactivity with a hydroxyl group. Go on.

Further, it has been found that an average reflectance of the absolute reflectance of the wavelength of 400 to 700 nm is controlled to be 6% or less, which is provided on the opposite side to the surface of the easy-adhesion layer of the polarizer, thereby providing high transmittance. Polyester film for polarizer protection. The inventors of the present invention have further studied and investigated based on these findings, and completed the present invention.

Representative examples of the present invention are shown below.

Item 1

A polyester film for protecting a polarizer is a polyester film having an easy-adhesion layer with a polarizer on one side, and the easy-adhesion layer contains a polyester resin (A) and a polyvinyl alcohol resin (B). a crosslinking agent (C), wherein the polyester resin (A) has an acid value of 20 KOHmg/g or less, and the polyvinyl alcohol-based resin (B) has a saponification degree of 60 to 85 mol%, and the polyester film is The average absolute reflectance of light having a wavelength of 400 to 700 nm on the opposite side of the single surface is 6% or less.

Item 2

The polyester film for protecting a polarizer according to the first aspect, wherein the opposite surface has a low refractive index layer having a lower refractive index than the polyester film.

Item 3

The polyester film for protecting a polarizer according to the first or second aspect, wherein the low refractive index layer is selected from the group consisting of a hard coat layer, an antiglare layer, and an antireflection layer.

Item 4

The polyester film for protecting a polarizer according to any one of the items 1 to 3, wherein the polyester resin (A) contains 1 to 15 mol% of 5-sulfoisophthalate in the dicarboxylic acid component. Formic acid component.

Item 5

The polyester film for polarizer protection according to any one of the items 1 to 4, wherein the crosslinking agent (C) is an isocyanate compound or a melamine compound.

Item 6

The polyester film for protecting a polarizer according to any one of the items 1 to 5, wherein the polyester resin (A), the polyvinyl alcohol resin (B), and the crosslinking agent (C) in the easy adhesion layer. The mass ratio satisfies the following formula; 0.8≦(A)/(B)≦5

2≦((A)+(B))/(C)≦50.

Item 7

A polarizing plate which is a polarizing plate having a polarizer protective film on both sides of a polarizer, and at least one of the polarizer protective films is a polarizer protective polyester film according to any one of items 1 to 6. .

Item 8

An image display device having at least one polarizing plate of item 7.

The polyester film for polarizer protection of the present invention is excellent in adhesion to a polyvinyl alcohol-based resin layer represented by a polarizer or an adhesive applied thereon. Further, the polyester film of the present invention has high light transmittance and can be suitably used as a protective film for a polarizer. By using the polyester film of the present invention as a protective film for a polarizer, it is possible to inexpensively produce a polarizing plate which is superior in durability and water barrier properties. Moreover, since the polarizing plate of the present invention is excellent in durability, it can be made thinner than ever. Therefore, by using the polarizing plate of the present invention, the liquid crystal display can be made thinner.

[Formation of the Invention]

(Polyester film)

The polyester film used as the substrate in the present invention is a film mainly composed of a polyester resin. Here, the "film mainly composed of a polyester resin" is a film formed of a resin composition containing 50% by mass or more of a polyester resin, and when it is blended with other polymers, it means 50 mass. When the polyester resin is copolymerized with other monomers, it means that it contains 50 mol% or more of the polyester structural unit. Preferably, the polyester film contains 90% by mass or more of the polyester resin, more preferably 95% by mass or more, still more preferably 100% by mass.

The material of the polyester resin is not particularly limited, but a copolymer obtained by polycondensation of a dicarboxylic acid component and a diol component, or a blended resin thereof can be used. Examples of the dicarboxylic acid component include terephthalic acid. Isophthalic acid, phthalic acid, 2,5-naphthalene dicarboxylic acid, 2,6-naphthalene dicarboxylic acid, 1,4-naphthalene dicarboxylic acid, 1,5-naphthalene dicarboxylic acid, diphenylcarboxylate Acid, diphenoxyethane dicarboxylic acid, diphenyl hydrazine carboxylic acid, hydrazine dicarboxylic acid, 1,3-cyclopentane dicarboxylic acid, 1,3-cyclohexane dicarboxylic acid, 1,4- Cyclohexanedicarboxylic acid, hexahydroterephthalic acid, hexahydroisophthalic acid, malonic acid, dimethylmalonic acid, succinic acid, 3,3-diethyl succinic acid, glutaric acid, 2 ,2-dimethylglutaric acid, adipic acid, 2-methyladipate, trimethyladipate, pimelic acid, sebacic acid, dimer acid, sebacic acid, suberic acid, ten Dialkyl dicarboxylic acid and the like.

Examples of the diol component constituting the polyester resin include ethylene glycol, propylene glycol, hexamethylene glycol, neopentyl glycol, 1,2-cyclohexane dimethanol, and 1,4-cyclohexane. Methanol, decamethyl glycol, 1,3-propanediol, 1,4-butanediol, 1,5-pentanediol, 1,6-hexanediol, 2,2-bis(4-hydroxyphenyl) ) propane, bis(4-hydroxyphenyl)anthracene, and the like.

The dicarboxylic acid component and the diol component constituting the polyester resin may be used alone or in combination of two or more. Further, other acid components such as trimellitic acid or other hydroxyl components such as trimethylolpropane may be appropriately added.

Specific examples of the polyester resin include polyethylene terephthalate, polytrimethylene terephthalate, polybutylene terephthalate, and polyethylene naphthalate. Among them, polyethylene terephthalate is preferred from the viewpoint of the balance between physical properties and cost. Further, in order to control optical characteristics such as polarizing properties, it is also preferable to contain other copolymerization components or other polymers. From the viewpoint of controlling the optical properties of the polyester film, examples of the copolymerizable component include diethylene glycol or a copolymerization component having a norbornene in a side chain.

The polyester film of the present invention is used as a film for polarizer protection It is preferably used to have high transparency. The transparency of the polyester film for polarizer protection of the present invention is preferably 90% or more, more preferably 91% or more, and even more preferably 92% or more. Further, the haze is preferably 3% or less, more preferably 2.5% or less, still more preferably 2% or less, and particularly preferably 1.5% or less. The total light transmittance of the polyester film can be measured by, for example, the method described in the examples below. However, the polyester film of the present invention having an antiglare layer to be described later is not limited by its characteristics.

In order to improve the workability such as slidability and winding property of the polyester film, blunt particles may be contained in the film. However, in order to maintain high transparency, it is preferred to minimize the content of blunt particles in the film. Therefore, it is preferred that the film layer contains only a plurality of layers of particles or that the film does not substantially contain particles, and the easy-adhesion layer which is only laminated on at least one side of the polyester film contains fine particles.

Further, the term "substantially free of particles", for example, in the case of inorganic particles, means 50 ppm or less, preferably 10 ppm or less, preferably under the detection limit, when the element derived from particles is quantitatively analyzed by fluorescent X-ray analysis. The content. In this case, even if the particles are not actively added to the base film, there is a contamination component from the foreign matter, a stain attached to the line or the device in the manufacturing process of the raw material resin or the film, and the film is mixed into the film. situation.

Further, when the base film is formed in a multi-layered structure, substantially no blunt particles are contained in the inner layer, and only two layers of blunt particles are contained in the outermost layer, which is capable of achieving both transparency and workability. good.

In the present invention, the thickness of the film is not particularly limited, but in order to reduce the thickness of the polarizing plate by thinning the display, the film is thin. The thickness is preferably 200 μm or less, more preferably 100 μm or less. On the other hand, in terms of maintaining the mechanical strength as the protective film, the film thickness is preferably 10 μm or more, more preferably 12 μm or more, and still more preferably 20 μm or more.

The polyester film to be a substrate may be a single layer or a laminate of two or more layers. Further, if it is within the range in which the effects of the present invention are exerted, various additives may be contained in the film as needed. Examples of the additive include an antioxidant, a light stabilizer, an antigelling agent, an organic wetting agent, an antistatic agent, an ultraviolet absorber, a surfactant, and the like. When the film has a laminated structure, it is also preferable to contain an additive in response to the function of each layer as needed. For example, in order to prevent photodegradation of the polarizer, it is preferable to add an ultraviolet absorber or the like to the inner layer.

The polyester film can be obtained, for example, by melt-extruding the above-mentioned polyester resin into a film form, and cooling and solidifying it by a casting drum to form a film. As the polyester film of the present invention, either an unstretched film or a stretched film can be used. However, from the viewpoint of durability of mechanical strength or chemical resistance, a stretched film is preferred. When the polyester film is a stretched film, the stretching method is not particularly limited, and a longitudinal uniaxial stretching method, a transverse uniaxial stretching method, a vertical and horizontal sequential biaxial stretching method, a vertical and horizontal simultaneous biaxial stretching method, or the like can be employed.

(easy to layer)

The polyester film of the present invention has an acid value of 20 KOHmg/min in at least a single-layer layer in order to improve adhesion to a polarizing plate and a polyvinyl alcohol-based resin layer such as a water-based adhesive provided on one surface or both surfaces thereof. An easy-adhesion layer formed of a polyester resin (A) having a g ratio of less than g, a polyvinyl alcohol-based resin (B) having a degree of saponification of 60 to 85 mol%, and a resin composition of the cross-linking agent (C).

Though it is not limited by the theory, it is presumed that the specific polyester resin (A) having an acid value of 20 KOHmg/g or less and the specific polyvinyl alcohol resin (B) having a saponification degree of 60 to 85 mol%. In combination with the crosslinking agent (C), the polyester resin and the polyvinyl alcohol resin each form a separate domain unit in the easy-adhesion layer to form a phase separation structure generally also referred to as a sea-island structure. It is presumed that by adopting the separation structure of such a domain unit, the adhesion to the polyester film by the sub-domain composed of the polyester resin, and the sub-domain composed of the polyvinyl alcohol-based resin The two functions of the adhesion to the polyvinyl alcohol-based resin layer are ideally achieved without damaging each other. It is presumed that the crosslinking agent (C) crosslinks and aggregates the polyvinyl alcohol-based resin (B) to promote and maintain the formation of the domain structure. The components of the easy-adhesion layer will be described in detail below.

(Polyester resin (A))

The polyester resin (A) used in the easy-adhesion layer of the present invention is a copolymer obtained by polycondensing a dicarboxylic acid component and a diol component, and the above-mentioned materials can be used as the dicarboxylic acid component and the diol component. From the viewpoint of improving the adhesion to the polyester film substrate, it is preferred to use a dicarboxylic acid component having the same or similar structure and properties as the dicarboxylic acid component in the polyester film as the polyester resin (A). Carboxylic acid component. In the case of using, for example, an aromatic dicarboxylic acid as the dicarboxylic acid component of the polyester film, an aromatic dicarboxylic acid is preferably used as the dicarboxylic acid component of the polyester resin (A). As such an aromatic dicarboxylic acid component, terephthalic acid and isophthalic acid are preferable. Further, another aromatic dicarboxylic acid may be added to the total dicarboxylic acid component in a range of 10 mol% or less to copolymerize.

Further, as the diol component of the polyester resin (A), it is preferred to Ethylene glycol and branched diols are constituent components. It is considered that it has a branched structure and contributes to stress relaxation in the easy-adhesion layer, and it is desirable to exhibit adhesion. The diol component of the above branch may, for example, be 2,2-dimethyl-1,3-propanediol, 2-methyl-2-ethyl-1,3-propanediol, or 2-methyl-2-butene. -1,3-propanediol, 2-methyl-2-propyl-1,3-propanediol, 2-methyl-2-isopropyl-1,3-propanediol, 2-methyl-2-n-hexyl -1,3-propanediol, 2,2-diethyl-1,3-propanediol, 2-ethyl-2-n-butyl-1,3-propanediol, 2-ethyl-2-n-hexyl-1, 3-propanediol, 2,2-di-n-butyl-1,3-propanediol, 2-n-butyl-2-propyl-1,3-propanediol, and 2,2-di-n-hexyl-1,3 - Propylene glycol and the like.

The molar ratio of the diol component of the above branch is preferably 10 mol%, and particularly preferably 20 mol%, based on the total diol component. On the other hand, the upper limit is preferably 80 mol%, more preferably 70 mol%, and particularly preferably 60 mol%. Further, if necessary, diethylene glycol, propylene glycol, butanediol, hexanediol or 1,4-cyclohexanedimethanol may be used in combination.

The polyester resin (A) used in the present invention is preferably a water-soluble or water-dispersible resin from the viewpoint of compatibility with the polyvinyl alcohol-based resin (B). In order to water-soluble or water-disperse the polyester resin, it is preferred to copolymerize a compound containing a hydrophilic group such as a sulfonate group or a carboxylate group. In addition, from the viewpoint of imparting hydrophilicity while controlling the reactivity with the crosslinking agent while maintaining the low acid value of the polyester resin (A), a dicarboxylic acid component having a sulfonate group is preferable. Examples of the dicarboxylic acid component having a sulfonate group include sulfo terephthalic acid, 5-sulfoisophthalic acid, 4-sulfonaphthalene isophthalic acid-2,7-dicarboxylic acid, and 5-(4-sulfophenoxy)isophthalic acid or an alkali metal salt thereof, which is preferably 5-sulfoisophthalic acid Dicarboxylic acid. The dicarboxylic acid component having a sulfonate group is preferably from 1 to 15 mol%, more preferably from 1.5 to 12 mol%, still more preferably from 2 to 10% in the dicarboxylic acid component of the polyester resin (A). Moer%. When the dicarboxylic acid component having a sulfonate group is at least the above lower limit, it is suitable for water solubility or water dispersion of the polyester resin. Further, when the dicarboxylic acid component having a sulfonate group is at most the above upper limit, the adhesion to the polyester film substrate is preferred.

The carboxylic acid group which is a reactive group of the polyester resin (A) and the crosslinking agent (C) is less preferred. It is considered that the reactivity with the crosslinking agent is lowered by reducing the carboxyl group reactive with the crosslinking agent, and as a result, the crosslinked polyvinyl alcohol resin can be maintained in incompletely mixed with the polyvinyl alcohol resin. The resulting fractal structure. From such a viewpoint, the acid value of the polyester resin (A) is 20 KOHmg/g or less, preferably 15 KOHmg/g or less, more preferably 10 KOHmg/g or less, still more preferably 8 KOHmg/g or less, and even more preferably 5 KOHmg / g or less. The acid value of the polyester resin (A) can be theoretically determined from the results of analysis by a component such as titration or NMR described later.

In order to control the acid value of the polyester resin (A) to the above range, it is preferred to reduce the amount of introduction of the carboxylate group for water solubility or water dispersion, or to use a hydrophilic group other than the carboxylate group. Or lower the carboxylic acid end concentration of the polyester resin. As a method of lowering the carboxylic acid terminal concentration of the polyester resin, a polyester resin having a terminal end of a carboxylic acid group or a polyester resin having a large number average molecular weight of a polyester resin is preferably used. Therefore, the number average molecular weight of the polyester resin (A) is preferably 5,000 or more, more preferably 6,000 or more, still more preferably 10,000 or more. Further, as a constituent component of the polyester resin (A), it is preferable to have three reductions. The content of the acid component of the above carboxyl group.

The glass transition temperature of the polyester resin (A) is not particularly limited, but is preferably 20 to 90 ° C, more preferably 30 to 80 ° C. When the glass transition temperature is at least the above lower limit, it is preferably a block resistance, and when the glass transition temperature is not more than the above upper limit, it is preferably an adhesion to a polyester film substrate.

In the easy-adhesion layer, the content of the polyester resin (A) is preferably 40% by mass or more and 90% by mass or less, more preferably 45% by mass or more and 85% by mass or less, and more preferably 50% by mass or more and 80% by mass or less. good. When the content of the polyester resin (A) is at least the above lower limit, the adhesion to the polyester film substrate is preferably at most the above-mentioned upper limit, and the adhesion to the polarizer or the aqueous resin is preferable.

(polyvinyl alcohol resin (B))

The polyvinyl alcohol-based resin is not particularly limited, and examples thereof include a polyvinyl alcohol obtained by saponifying polyvinyl acetate; a derivative thereof; and a saponified product of a copolymer of a monomer copolymerizable with vinyl acetate. A modified polyvinyl alcohol obtained by subjecting polyvinyl alcohol to acetalization, urethanization, etherification, grafting, phosphation, or the like; Examples of the monomer include unsaturated carboxylic acids such as maleic acid (anhydride), fumaric acid, crotonic acid, itaconic acid, and (meth)acrylic acid, and esters thereof; and α-olefins such as ethylene and propylene. Allylsulfonic acid (sodium), sodium sulfonate (monoalkyl maleate), sodium alkyl maleate disulfonate, N-methylol acrylamide, acrylamide sulfonate An alkali salt, N-vinyl pyrrolidine, N-vinyl pyrrolidine derivative or the like. These polyvinyl alcohol-based resins may be used alone or in combination of two or more.

As the polyvinyl alcohol-based resin (B) used in the present invention And exemplified by a vinyl alcohol-vinyl acetate copolymer, a vinyl alcohol-vinyl butyral copolymer, an ethylene-vinyl alcohol copolymer, among which vinyl alcohol-vinyl acetate copolymer, ethylene-ethylene is preferred. Alcohol copolymer. The degree of polymerization of the polyvinyl alcohol-based resin (B) is not particularly limited, but the degree of polymerization is preferably 3,000 or less from the viewpoint of the viscosity of the coating liquid.

The copolymerization ratio of vinyl alcohol is expressed by the degree of saponification. The degree of saponification of the polyvinyl alcohol-based resin (B) of the present invention is preferably 60 mol% or more and 85 mol% or less, more preferably 65 mol% or more and 83 mol% or less, and 68 mol% or more and 80 mol%. More preferably, 70 mol% or more and less than 80 mol% are more preferably, 71 mol% or more and 78 mol% or less are more preferably 73 mol% or more and 75 mol% or less. When the degree of saponification of the polyvinyl alcohol-based resin (B) is at least the above lower limit, it is more suitable for forming a crosslinked structure with the crosslinking agent (C). In addition, when the degree of saponification of the polyvinyl alcohol-based resin (B) is not more than the above upper limit (or less than), the compatibility with the polyester resin (A) can be more desirable. The degree of saponification of the vinyl alcohol-based resin can be determined by analysis of the composition of NMR by the amount of alkali consumed by hydrolysis of a copolymerization unit such as vinyl acetate.

The content of the polyvinyl alcohol-based resin (B) is preferably 10% by mass or more and 60% by mass or less in the easy-adhesion layer, more preferably 15% by mass or more and 55% by mass or less, and more preferably 20% by mass or more and 50% by mass or less. Better. When the content of the polyvinyl alcohol-based resin (B) is at least the above lower limit, the adhesion to the polarizing plate or the aqueous resin is preferably at most the above-mentioned upper limit, and the adhesion to the polyester film substrate is preferable.

(crosslinking agent (C))

The cross-linking agent (C) is not particularly limited as long as it is cross-linkable with a hydroxyl group, and examples thereof include a melamine-based, an isocyanate-based, and a carbodiimide-based compound. A compound such as an oxazoline system or an epoxy group. From the viewpoint of stability over time of the coating liquid, melamine, isocyanate or carbodiimide is preferred. An oxazoline compound. Further, the crosslinking agent is preferably a melamine-based compound or an isocyanate-based compound which is suitable for crosslinking reaction with a hydroxyl group of the polyvinyl alcohol-based resin (B). It is considered that since a melamine-based compound or an isocyanate-based compound reacts with a hydroxyl group with respect to a carbodiimide-based crosslinking agent, it is more suitable for a polyvinyl alcohol-based resin having a hydroxyl group as a functional group. (B) The reason for forming a crosslinked structure. Among them, an isocyanate compound is particularly preferable from the viewpoint of forming a crosslinking reaction with a hydroxyl group of a polyvinyl alcohol-based resin and having excellent transparency. Further, in order to promote the crosslinking reaction, it is also necessary to appropriately use a catalyst or the like.

As the isocyanate compound, a low molecular or high molecular diisocyanate or a trivalent or higher polyisocyanate can be used. For example, examples of the isocyanate compound include 2,4-toluene diisocyanate, 2,6-toluene diisocyanate, 4,4'-diphenylmethane diisocyanate, and 2,4'-diphenylmethane diisocyanate. , 2,2'-diphenylmethane diisocyanate, 1,5-naphthalene diisocyanate, 1,4-naphthalene diisocyanate, phenyl diisocyanate, tetramethyl dimethyl diisocyanate, 4, 4'- Diphenyl ether diisocyanate, 2-nitrodiphenyl-4,4'-diisocyanate, 2,2'-diphenylpropane-4,4'-diisocyanate, 3,3'-dimethyldiphenyl An aromatic diisocyanate such as methyl methane-4,4'-diisocyanate, 4,4'-diphenylpropane diisocyanate or 3,3'-dimethoxydiphenyl-4,4'-diisocyanate, Aromatic aliphatic diisocyanates such as benzodimethyl diisocyanate and isophorone diiso Cyanate esters and alicyclic diisocyanates such as 4,4-dicyclohexylmethane diisocyanate and 1,3-bis(isocyanatemethyl)cyclohexane, hexamethylene diisocyanate, and 2,2,4- An aliphatic diisocyanate such as trimethylhexamethylene diisocyanate or a terpolymer of the isocyanate compound. Further, an excessive amount of the isocyanate compound and a low molecular weight active hydrogen compound such as ethylene glycol, propylene glycol, trimethylolpropane, glycerin, sorbitol, ethylenediamine, monoethanolamine, diethanolamine or triethanolamine, or A terminal isocyanate group-containing compound obtained by reacting a polymer active hydrogen compound such as a polyester polyol, a polyether polyol or a polyamine.

As the crosslinking agent (C) used in the present invention, a blocked isocyanate compound is also preferred. By adding a blocked isocyanate-based compound, the stability over time of the coating liquid can be more preferably improved.

The blocked isocyanate compound can be prepared and obtained by subjecting the above isocyanate compound and a blocking agent to an addition reaction by a conventionally known method. Examples of the isocyanate blocking agent include phenols such as phenol, cresol, xylenol, resorcin, nitrophenol, and chlorophenol; thiophenols such as thiophenol and methylthiophenol; Anthraquinones such as methyl ethyl ketone oxime and cyclohexanone oxime; alcohols such as methanol, ethanol, propanol and butanol; halogen-substituted alcohols such as chlorohydrin and 1,3-dichloro-2-propanol; a tertiary alcohol such as triamyl alcohol; 3,5-dimethylpyrazole, 3-methylpyrazole, 4-bromo-3,5-dimethylpyrazole, 4-nitro-3,5-di Pyrazole-based compounds such as methylpyrazole; triazole-based compounds such as 1,2,4-triazole; ε-caprolactam, δ-valeroinamide, γ-butylide, β-propyl Indoleamines such as decylamine; aromatic amines; quinone imines; acetamylacetone, acetamidine acetate, ethyl malonate, malonic acid diester (dimethyl malonate, propylene glycol) Diethyl acid, C Active methylene compounds such as di-n-butyl diacid, di-ethylhexyl malonate; mercaptans; imines; ureas; diaryl compounds; sodium bisulfite.

The content of the crosslinking agent (C) is preferably 2% by mass or more and 50% by mass or less in the easy-adhesion layer, more preferably 5% by mass or more and 40% by mass or less, and still more preferably 8% by mass or more and 30% by mass or less. . When the content of the crosslinking agent (C) is at least the above lower limit, it is suitable for crosslinking formation of a polyvinyl alcohol-based resin, and when it is at most the above upper limit, it is suitable for exhibiting an adhesive effect by a binder resin.

The blending ratio (A)/(B) of the polyester resin (A) and the polyvinyl alcohol resin (B) is preferably 0.8 to 5 by mass ratio, more preferably 1 to 4, and 2 to 4 Better, 2.5~3.5 is especially good. When it is at least the above lower limit, the adhesion to the polyester film substrate is preferably at least the above upper limit, and the adhesion to the polarizer or the water-based resin is preferable.

The blend ratio ((A) + (B)) / (C) of the polyester resin (A) and the polyvinyl alcohol resin (B) to the crosslinking agent (C) is preferably a mass ratio. 2~50, 5~40 is better, 8~30 is better. ((A)+(B))/(C) is preferably at least the above lower limit, and is suitable for exhibiting an adhesive effect of the binder resin component. When the thickness is less than or equal to the above upper limit, the effect of the phase separation is preferable.

Since the above-mentioned composition is used as the easy-adhesive layer of the present invention, the polarizer, the aqueous adhesive, especially the polyvinyl alcohol-based polarizer and the aqueous adhesive exhibit the same high adhesion to triethyl fluorenyl cellulose. Specifically, the residual area after the first peeling of the aqueous adhesive by the adhesion test described later is preferably 90% or more, more preferably 95%. The above is more preferably 100%, and the residual area after 5 consecutive peelings is preferably 75% or more, more preferably 85% or more, still more preferably 95% or more, and the residual area after 10 consecutive peelings is 50%. The above is more preferably 80% or more, more preferably 90% or more, still more preferably 93% or more, and particularly preferably 95% or more.

(additive)

In the easy-adhesion layer of the present invention, well-known additives such as a surfactant, an antioxidant, a catalyst, a heat-resistant stabilizer, a weather-resistant stabilizer, an ultraviolet absorber, and an organic one may be added to the extent that the effects of the present invention are not impaired. Slip agents, pigments, dyes, organic or inorganic particles, antistatic agents, nucleating agents, and the like.

In the present invention, in order to further improve the anti-adhesion property of the easy-adhesion layer, it is also preferable to add particles to the easy-adhesion layer. Examples of the particles contained in the easy-adhesion layer in the present invention include titanium oxide, barium sulfate, calcium carbonate, calcium sulfate, cerium oxide, aluminum oxide, talc, kaolin, clay, and the like, or a mixture thereof. And other common inorganic particles, such as calcium phosphate, mica, hectorite, zirconia, tungsten oxide, lithium fluoride, calcium fluoride, other inorganic particles, or styrene, acrylic, melamine An organic polymer-based particle such as a benzoguanamine-based or an fluorenone-based compound.

The average particle diameter of the particles in the easy-adhesion layer (the average particle diameter based on the number of SEMs, the same applies hereinafter) is preferably 0.04 to 2.0 μm, more preferably 0.1 to 1.0 μm. When the average particle diameter of the blunt particles is less than 0.04 μm, the formation of irregularities on the surface of the film is insufficient, and workability such as slidability or winding property of the film is lowered, and workability at the time of bonding is lowered. The situation. On the other hand, if it exceeds 2.0 μm, particle detachment tends to occur. The concentration of the particles in the easy-adhesion layer is preferably from 1 to 20% by mass in the solid content, and more preferably from 5 to 15% by mass.

In the present invention, the thickness of the easy-adhesion layer can be appropriately set in the range of 0.001 to 2 μm, but it is both workability and adhesion, preferably in the range of 0.01 to 1 μm, more preferably 0.02 to 0.8 μm, and more preferably 0.05~0.5μm. If the thickness of the easily-adherent layer is less than 0.01 μm, the adhesion is insufficient. If the thickness of the easily-adhesive layer exceeds 2 μm, blocking may occur.

(low refractive index layer)

In order to increase the light transmittance of the polyester film for polarizer protection of the present invention, the average absolute reflectance of light having a wavelength of 400 to 700 nm opposite to the surface on which the adhesion-prone layer is provided is preferably 6% or less. The average absolute reflectance is preferably 5% or less, and more preferably 4.5% or less. If the average absolute reflectance is more than 6%, the reflection of visible light to be penetrated on the surface of the film increases, and the transmittance decreases. On the other hand, when it is 6% or less, reflection on the surface of the film is suppressed, and a polyester film for protecting a polarizer having high transmittance can be provided.

The method for controlling the average absolute reflectance within the above range is not particularly limited, but is preferably an area layer low refractive index layer which is opposite to the surface of the polyester film of the present invention which is provided with an easy-to-attach layer. The low refractive index layer refers to a layer having a lower refractive index than the polyester film of the substrate, and more specifically, a layer having a refractive index of 1.60 or less. It is more preferable if the refractive index is 1.55 or less. The lower limit of the refractive index is not particularly limited, and is practically preferably 1.20 or more, more preferably 1.25 or more.

The material used for the low refractive index layer is not particularly limited, but a polyester resin, a polyurethane resin, an acrylic resin, a polyvinyl alcohol resin, a polycarbonate resin, or a fluorine resin. An anthrone-based resin or the like is suitable for use. These resins may be resin compounds which are polymerized and/or reacted by drying, heat, chemical reaction, or irradiation of any of electron beams, radiation, and ultraviolet rays, and known materials may be used. Among these, the polyurethane resin, the acrylic resin, and the fluorine resin have a relatively low refractive index and can be suitably used.

(polyurethane resin)

The urethane resin used in the low refractive index layer preferably contains at least a polyol component and a polyisocyanate component as a constituent component, and further contains a chain extender as needed. The urethane resin is a polymer compound mainly composed of such a constituent component and copolymerized by a urethane bond.

Examples of the polyol component include polycarboxylic acids (for example, malonic acid, succinic acid, adipic acid, sebacic acid, fumaric acid, maleic acid, terephthalic acid, isophthalic acid, etc.) or the like. Anhydrides and polyols (for example: ethylene glycol, diethylene glycol, triethylene glycol, propylene glycol, butanediol, 1,3-butanediol, 1,4-butanediol, 2,3-butyl Polyester polyols obtained by the reaction of diol, neopentyl glycol, 1,6-alkanediol, etc., polyethylene glycol, polypropylene glycol, polyethylene glycol, polytetramethylene ether glycol, polyhexamethylene A polyether polyol such as methyl ether glycol, a polycarbonate polyol, a polyolefin polyol, or an acrylic polyol. Among them, the polyol component which is a constituent component of the urethane resin is preferably an aliphatic polycarbonate polyol which is excellent in heat resistance and hydrolysis resistance. In the optical use of the present invention, From the viewpoint of preventing yellowing, it is also preferred to use an aliphatic polycarbonate polyol.

(polyester resin)

The polyester resin used for the low refractive index layer is exemplified by the following. The number average molecular weight of the polyester resin is preferably 15,000 or more. When the number average molecular weight is low, the hydrolysis of the terminal carboxylic acid group promotes hydrolysis, and not only the adhesion under high temperature and high humidity is not obtained, but also the adhesion to the base film is lowered. Further, the number average molecular weight is more preferably 20,000 or more, and further, as long as it can be produced, it is preferably higher. However, if the number average molecular weight is increased, the solubility in the coating liquid may be lowered. Therefore, the number average molecular weight is preferably 60000 or less.

Polyester resin, examples of the acid component include terephthalic acid, isophthalic acid, phthalic acid, phthalic anhydride, 2,6-naphthalene dicarboxylic acid, and 1,4-cyclohexanedicarboxylic acid. Adipic acid, azelaic acid, trimellitic acid, pyromellitic acid, dimer acid, sodium 5-sulfoisophthalate, sodium 4-sulfonaphthalene-2,7-dicarboxylate, and the like. Examples of the diol component include ethylene glycol, propylene glycol, 1,4-butanediol, neopentyl glycol, diethylene glycol, 1,6-hexanediol, 1,4-cyclohexanedimethanol, and Toluene diol, ethylene oxide adduct of bisphenol A, and the like.

The polyester resin can be used by dissolving or dispersing in water, or a water-soluble organic solvent (for example, an alcohol containing less than 50% by mass of an alcohol, an alkyl stilbene, a ketone system, or an ether system), or an organic solvent (for example: Toluene, ethyl acetate, etc.).

In the case where a polyester resin is used as a water-based coating liquid, Although a water-soluble or water-dispersible polyester resin is used, for the purpose of such water-solubility or water-dispersion, it is preferred to copolymerize a compound containing a sulfonate group or a compound containing a carboxylate group. Therefore, in addition to the use of the above-mentioned dicarboxylic acid component, in order to impart water dispersibility to the polyester, it is preferred to use 5-sulfoisophthalic acid or an alkali metal salt thereof in the range of 1 to 10 mol%, for example, , sulfoterephthalic acid, 5-sulfoisophthalic acid, 4-sulfonaphthalene isophthalic acid-2,7-dicarboxylic acid and 5-(4-sulfophenoxy)isophthalic acid Or an alkali metal salt thereof.

In order to make the number average molecular weight of the polyester resin 15000 or more and to have a glass transition temperature which suppresses the degree of sticking, it is preferred to introduce a branched structure into the polyester resin. However, if the branch structure is increased, the acid value tends to increase. Therefore, the polyester resin is preferably a molar ratio of 5.0 mol% or less in the total dicarboxylic acid component, which has a carboxyl group of 3 or more/1 molecule or a hydroxyl group of 3 or more/1 molecule. More preferably, it is 1.0 mol% or less.

(acrylic resin)

The acrylic resin to be used for the low refractive index layer is not particularly limited, and a polymer containing a polymerizable monomer having a carbon-carbon double bond typified by an acrylic or methacrylic monomer can be used. These may be any of a homopolymer or a copolymer. Also included are copolymers of such polymers with other polymers (e.g., polyesters, polyurethanes, etc.). For example, block copolymers, graft copolymers. Or also includes a polymer obtained by polymerizing a polymerizable monomer having a carbon-carbon double bond in a polyester solution or a polyester dispersion (sometimes a mixture of polymers, as the case may be). Similarly, it is also included in the polyurethane solution and the polyurethane dispersion to have carbon- A polymer obtained by polymerizing a polymerizable monomer of a carbon double bond (sometimes a mixture of polymers as the case may be). Also included is a polymer obtained by polymerizing a polymerizable monomer having a carbon-carbon double bond in another polymer solution or dispersion, as the case may be a polymer mixture. Further, in order to increase the total light transmittance more efficiently, a fluorine atom-containing compound having a low refractive index can also be used.

The polymerizable monomer having a carbon-carbon double bond is not particularly limited, and examples of the particularly representative compound include acrylic acid, methacrylic acid, crotonic acid, itaconic acid, fumaric acid, and Malay. Monomers containing various carboxyl groups such as acid and citraconic acid, and salts thereof; 2-hydroxyethyl (meth)acrylate, 2-hydroxypropyl (meth)acrylate, (meth)acrylic acid 4 - various hydroxyl group-containing monomers such as hydroxybutyl ester, hydroxyfumaric acid monobutyl ester, hydroxy itaconic acid monobutyl ester; methyl (meth) acrylate, ethyl (meth) acrylate, (methyl a variety of (meth) acrylates such as propyl acrylate, butyl (meth) acrylate, lauryl (meth) acrylate; (meth) acrylamide, diacetone acrylamide, N-hydroxyl Various nitrogen-containing compounds such as acrylamide or (meth)acrylonitrile; various styrene derivatives such as styrene, α-methylstyrene, divinylbenzene, vinyltoluene, and vinyl acetate , various vinyl esters such as vinyl propionate; γ-methacryloxypropyltrimethoxydecane, vinyl trimethoxy Various fluorene-containing polymerizable monomers such as decane; phosphorus-containing vinyl monomers; vinyl chloride, vinylidene chloride, vinyl fluoride, divinylidene fluoride, chlorotrifluoroethylene, tetrafluoroethylene, Various halogenated vinyls such as chlorotrifluoroethylene and hexafluoropropylene; and various conjugated dienes such as butadiene.

Further, in the case where the low refractive index layer is hard-coated, it is preferred to use an acrylic resin which is hardened by electron beam or ultraviolet rays. The acrylic resin hardened by electron beam or ultraviolet light means an acrylate-based functional group, for example, a lower molecular weight polyester resin, a polyether resin, an acrylic resin, an epoxy resin, a urethane resin, Oligomers or prepolymers such as (meth) acrylates of polyfunctional compounds such as alkyd resins, acetal resins, polybutadiene resins, polythiol polyene resins, and polyhydric alcohols, and as reactive diluents Monofunctional monomers and polyfunctional monomers containing ethyl (meth)acrylate, ethylhexyl (meth)acrylate, styrene, methylstyrene, N-vinylpyrrolidine, and the like, for example, three Hydroxymethylpropane tri(meth)acrylate, hexanediol (meth)acrylate, tripropylene glycol di(meth)acrylate, diethylene glycol di(meth)acrylate, pentaerythritol tris(methyl) Acrylate, dipentaerythritol hexa(meth) acrylate, 1,6-hexanediol di(meth) acrylate, neopentyl glycol di(meth) acrylate, and the like.

In the case of an electron beam or an ultraviolet curable resin, in the above-mentioned resin, a acetophenone, a diphenyl ketone, a M. benzoyl benzoate, and α- may be used in combination as a photopolymerization initiator. Pentamidine, tetramethylthiuram monosulfide, thioxanthone, or n-butylamine, triethylamine, tri-n-butylphosphine, etc. as a photosensitizer. The amount of the photopolymerization initiator to be added is preferably 0.1 to 10 parts by mass based on 100 parts by mass of the electron beam or the ultraviolet curable resin.

The curing method of the coating film is not particularly limited, but it is preferably carried out by ultraviolet irradiation. In the case of hardening by ultraviolet rays, it is preferred to use ultraviolet rays having a wavelength range of 190 to 380 nm. By purple The hardening of the outer wire can be carried out, for example, by using a metal halide lamp, a high pressure mercury lamp, a low pressure mercury lamp, an ultrahigh pressure mercury lamp, a carbon arc lamp, a black fluorescent lamp, or the like. Specific examples of the electron beam source include various electron linear accelerators such as a Cockcroft-Walton type, a Van de graft type, a resonant transformer type, an insulating nuclear transformer type, a linear type, a Dynamitron type, and a high frequency type.

(fluororesin)

The fluorine-containing resin used as the low refractive index layer is not particularly limited, but the following materials are suitable for use. As the fluorine-containing resin, for example, 1-(meth)acryloxyl-1-perfluoroalkylmethane, 1-(meth)acryloxy-2-perfluoroalkylethane, 1 is preferable. , 10-bispropenyloxy-1,1,10,10-tetrahydroperfluorodecane, 1,10-bisbispropenyloxy-2,9-dihydroxy-4,4,5,5,6 6,6,7-octafluorodecane, 1,9-dibispropenyloxy-2,10-dihydroxy-4,4,5,5,6,6,7,7-octafluorononane, 2,9-bisbispropenyloxy-1,10-dihydroxy-4,4,5,5,6,6,7,7-octafluorodecane, 1,2-di(methyl)propene oxime 3--3-perfluoroalkylbutane, 2-hydroxy-1H,1H,2H,3H,3H-perfluoroalkyl-2',2'-bis{(methyl)acryloxymethyl}propyl Acid ester, α,ω-di(meth)acryloxymethyl perfluoroalkane, α,β,ψ,ω-肆{(methyl)acryloxy}-αH,αH,βH,γH, γH, χH, χH, ψH, ωH, ωH-perfluoroalkane, and the like.

(polyvinyl alcohol resin)

The polyvinyl alcohol resin used in the low refractive index layer is not particularly limited, and the same one as that of the user of the easy-to-layer layer in the present specification can be used.

In order to reduce the refractive index of the low refractive index layer, conventionally known organic or inorganic fine particles can be used. For example, cerium oxide fine particles, organic resin fine particles, and the like. Further, it is also preferred to use hollow ceria particles. The hollow ceria particles, which are cerium oxide (cerium oxide, SiO ₂ ), are formed into a nearly spherical shape, and have hollow portions in the outer casing. The average particle diameter of the hollow ceria particles is preferably from 10 to 100 nm, more preferably from 20 to 60 nm. In the case where the average particle diameter of the hollow ceria particles is less than 10 nm, the production of the hollow ceria particles is difficult. On the other hand, in the case where the average particle diameter is larger than 100 nm, the scattering of light is increased, the reflection in the film is increased, and the surface reflectance is increased.

The film thickness of the low refractive index layer is preferably 400 ≦ 4 n‧d (nm) ≦ 700. (wherein n represents the refractive index of the low refractive index layer, and d represents the film thickness.) Although it can be used even if it exceeds this range, by satisfying this range, the reflection of the surface can be satisfactorily suppressed, and the transmittance can be improved. .

The low refractive index layer and the polyester film may have another layer, and an anchor coat layer in which the polyester film and the low refractive index layer are in close contact with each other is also a preferred embodiment.

The low refractive index layer may be a functional layer having at least one of hard coat properties, antiglare properties, antireflection properties, and antistatic properties. In this case, there may be other layers between the functional layer and the polyester film. The low refractive index layer of the functional layer can be provided with another layer between the polyester film and the low refractive index layer, and the other layer is integrated with the low refractive index layer to form hard coating, anti-glare, anti-reflection A functional layer of at least one function of properties and antistatic properties. In any configuration, the low refractive index layer is disposed on the outermost layer, and is preferable in terms of improving the transmittance of the film. The following description is for the functional layer, but it is of course not limited to the configuration shown below.

(hard coating)

The hard coatability of the low refractive index layer is as described above. Further, as the resin used for the hard coat layer, it is preferred to use the above-mentioned resin which is hardened by electron beam or ultraviolet light, and is preferably an acrylic resin which is hardened by electron beam or ultraviolet light.

(anti-glare layer)

As a method of imparting anti-glare property to the low refractive index layer, a well-known technique can be used. For example, a concave-convex shape can be formed on the polyester film to scatter external light, thereby preventing a decrease in visibility due to reflection of external light or reflection of an image. As a method of forming the unevenness, there is a method of applying a resin containing a large particle diameter or a cohesive particle, forming a concave-convex shape on the surface of the film, or transferring a concave-convex shape by laminating a film having irregularities on the surface of the layer. A method of forming an anti-glare layer, and a method of forming a concavity and convexity by imprinting with a nanoparticle without using the above-mentioned particles may be used in combination of one kind or two or more types.

As the resin used for the antiglare layer, the same thing as the above-described electron beam or ultraviolet curable resin can be used. One type or two or more types of the resins described above can be used. Further, in order to adjust physical properties such as plasticity and surface hardness, a resin which is not cured by electron beams or ultraviolet rays may be mixed. Examples of the resin which is not hardened by electron beam or ultraviolet rays include polyurethane, cellulose derivative, polyester, acrylic resin, polyvinyl butyral, polyvinyl alcohol, polyvinyl chloride, polyvinyl acetate, and poly Carbonate, polyamine, and the like.

Specific examples of the particles used in the antiglare layer include particles of an inorganic compound such as cerium oxide particles, alumina particles, and TiO ₂ particles, or polymethyl methacrylate particles or acrylic acid-styrene copolymer. Particles, crosslinked acrylic particles, melamine particles, crosslinked melamine particles, polycarbonate particles, polyvinyl chloride particles, Benzoguanamine particles, crosslinked benzoguanamine particles, polystyrene particles, crosslinked polyphenylene Resin particles such as ethylene particles. In terms of shape, it is suitable to use true spherical particles having the same shape of the surface protrusions, but an amorphous material such as a layered inorganic compound such as talc or bentonite may be used. Further, two or more different types of particles may be used in combination. The material type may be two or more, and the particle diameter may be two or more types, and is not limited.

The particle diameter of the particles used in the antiglare layer is, for example, 0.5 to 10 μm, more preferably 0.5 to 5 μm, more preferably 0.5 to 3 μm, and even more preferably 0.5 to 1.5 μm. Further, the content of the particles is preferably 1 to 50% by weight, more preferably 2 to 30% by weight, based on the resin.

The film thickness of the antiglare layer is preferably 0.5 μm to 20 μm, more preferably 1 μm to 20 μm, and still more preferably 1 μm to 10 μm.

The haze of the polarizer for protecting the polarizer having the antiglare layer of the present invention is preferably from 1 to 50%. 1~30% is better, 1~10% is better.

As an anti-glare layer used in the present invention, it is also suitable to use Japanese Patent Laid-Open No. Hei 6-18706, Japanese Patent Laid-Open No. Hei 10-20103, Japanese Patent Laid-Open No. 2009-227735, Japanese Patent Laid-Open No. 2009-86361, Japanese Patent Laid-Open No. 2009-80256, and Japan. An anti-glare layer described in JP-A-2011-81217, JP-A-2010-204479, JP-A-2010-181898, JP-A-2011-197329, JP-A-2011-197330, and JP-A-2011-215393.

(anti-glare anti-reflection layer)

An antiglare layer may be laminated between the low refractive index layer of the present invention and the polyester film to form an antiglare antireflection layer. a layer of anti-glare anti-reflection layer, Well-known techniques can be used. At this time, the effect of the present invention can be ensured by the fact that the refractive index of the antiglare layer is higher than that of the low refractive index layer.

The anti-glare anti-reflection layer used in the present invention is also preferably disclosed in JP-A-2001-281405, JP-A-2004-125958, JP-A No. 4225675, JP-A-2009-47938, JP-A-2009-157234, and the like. Anti-glare anti-reflection layer.

(anti-reflection layer)

Between the low refractive index layer and the polyester film, a medium refractive index layer, a high refractive index layer, or only a high refractive index layer may be laminated from the polyester film side to form an antireflection layer. As the antireflection layer, in addition to the above, it is also possible to laminate using a well-known technique, without departing from the effects of the present invention.

(high refractive index layer, medium refractive index layer)

The high refractive index layer and the medium refractive index layer of the antireflection layer of the polyester film of the present invention are composed of an inorganic material, an organic material, and the like. The refractive index of the high refractive index layer is preferably higher than the low refractive index layer, and is preferably 1.60 or more, and preferably 1.60 to 1.90. If it is less than 1.60, a sufficient antireflection effect cannot be obtained, and if it exceeds 1.90, the resin layer is difficult to form by wet coating. The refractive index of the medium refractive index layer is preferably lower than the high refractive index layer and higher than the low refractive index layer, and is preferably in the range of 1.50 to 1.65.

The material constituting the high refractive index layer and the medium refractive index layer is not particularly limited, but an inorganic material and an organic material can be used. The method for forming the high refractive index layer and the medium refractive index layer may be a vacuum evaporation method or a sputtering method using a chemical vapor deposition (CVD) method or a physical vapor deposition (PVD) method, in particular, a physical vapor deposition method. And use a transparent film of inorganic oxide, but preferably borrow A method of coating by total wetness.

In the case of wet coating, the high refractive index layer is preferably coated with inorganic particles containing an oxide containing at least one metal selected from the group consisting of Ti, Zr, In, Zn, Sn, Al, and Sb. A curable resin having a trifunctional or higher polymerizable group (which can be used by a user of a hard coat layer of the present invention), a solvent, and a coating composition of a polymerization initiator, which are dried by a heating and ionizing radiation. Or use two methods to harden and form. When a curable resin or an initiator is used, a high refractive index layer can be formed by a polymerization reaction by heat and/or ionizing radiation after application to harden the curable resin. The medium refractive index layer can be formed using, in particular, the same material or the like, in addition to the refractive index of the high refractive index layer.

(inorganic particles)

As the inorganic fine particles, an oxide of a metal (for example, Ti, Zr, In, Zn, Sn, Sb, or Al) is preferable, and from the viewpoint of the refractive index, the fine particles of zirconia are preferable. However, from the viewpoint of conductivity, it is preferred to use inorganic fine particles having an oxide of at least one of Sb, In, and Sn as a main component. It can be adjusted to a predetermined refractive index by changing the amount of inorganic particles. The average particle diameter of the inorganic fine particles in the layer is preferably from 1 to 120 nm, more preferably from 5 to 100 nm, even more preferably from 10 to 100 nm, in the case where zirconia is used as a main component. Within this range, the haze is suppressed, and the dispersion stability is improved, and the adhesion between the upper layer and the outer layer is preferably improved by the appropriate unevenness of the surface.

The inorganic fine particles having zirconia as a main component have a refractive index of preferably 1.9 to 2.8, more preferably 2.1 to 2.8, and most preferably 2.2 to 2.8. Addition of inorganic particles The amount of addition is different for each layer, and the high refractive index layer is preferably 40 to 90% by mass, more preferably 50 to 85% by mass, and more preferably 60 to 80% by mass based on the total solid content of the high refractive index layer. The medium refractive index layer is from 1 to 60% by mass, preferably from 3 to 50% by mass, based on the total solid content of the medium refractive index layer.

The thickness of the antireflection layer including the low refractive index layer and the high refractive index layer varies depending on the structure of the antireflection layer, but it is preferable that each layer has the same thickness as the visible light wavelength or less. For example, when exhibiting a reflection effect of reducing visible light, the optical film thickness nH‧d of the high refractive index layer is designed to be 500 ≦ 4 nH ‧ d (nm) ≦ 750, and the optical film thickness of the low refractive index layer is nL ‧ d It is 400≦4nL‧d(nm)≦650. However, nH and nL are the refractive indices of the high refractive index layer and the low refractive index layer, respectively, and d is the thickness of the layer.

As the antireflection layer used in the present invention, it is also possible to use Japanese Patent Laid-Open No. 2003-177209, Japanese Patent Laid-Open No. 2008-262187, Japanese Patent Laid-Open No. 2010-170089, Japanese Patent Laid-Open No. 2004-30971, Japanese Patent Laid-Open No. 2011-191735, and Japan. The antireflection layer described in JP-A-2004-322380, JP-A-2009-3354, JP-A-2010-72039, and JP-A-2010-256705.

In the low refractive index layer of the present invention, in addition to the above-described contents, other components may be contained as needed within a range that does not impair the effects of the invention. The other components are not limited, and for example, inorganic or organic pigments, polymers, polymerization initiators, polymerization inhibitors, antioxidants, dispersants, surfactants, photosetters, leveling agents, antistatic agents, ultraviolet rays may be added. Absorbent, catalyst, infrared absorber, flame retardant, defoamer, Conductive fine particles, conductive resin, and the like.

The low refractive index layer of the present invention may be provided in a single type as described above, or may be combined with a plurality of functions.

(Manufacture of easy-adhesive polyester film for polarizer protection)

The method for producing the easily-adhesive polyester film for protecting a polarizer of the present invention is described by taking a polyethylene terephthalate (hereinafter abbreviated as PET) film as an example, but it is of course not limited thereto.

The PET resin is sufficiently vacuum-dried, and then supplied to an extruder, and the molten PET resin of about 280 ° C is melt-extruded into a sheet shape from a T-die to a rotary cooling roll, and solidified by electrostatic application to obtain an unstretched PET sheet. . The unstretched PET sheet may be composed of a single layer or a multilayer formed by a co-extrusion method.

The obtained unstretched PET sheet was subjected to uniaxial stretching or biaxial stretching to crystallize it. For example, in the case of biaxial stretching, the roller heated to 80-120 ° C extends 2.5 to 5.0 times in the longitudinal direction, and after obtaining the uniaxially stretched PET film, the end of the film is clamped by the clamp, and is guided to the heated The hot air zone of 80~180 °C extends 2.5 to 5.0 times in the width direction. Moreover, in the case of uniaxial stretching, it extends 2.5 to 5.0 times in the tenter. After the extension, it is guided to a heat treatment zone of 140 to 240 ° C, and heat treatment is performed for 1 to 60 seconds to complete the crystallization alignment.

The easy-to-layer layer can be set after the film is manufactured or in the manufacturing step. In particular, from the viewpoint of productivity, it is preferred to apply a coating liquid to form an easy-adhesion layer at any stage of the film production step, that is, at least one side of the PET film which is not stretched or uniaxially stretched.

a method for coating the coating liquid on a PET film, Use any method known in the art. For example, reverse roll coating, gravure coating, kiss coating, die coating, roll brushing, spray coating, air knife coating, wire bar coating, pipe blade (pipe) Doctor) method, dip coating method, curtain coating method, etc. These methods or combinations can be used alone for coating.

In the present invention, the thickness of the finally obtainable adhesive layer is preferably from 0.03 to 0.20 g/m ² . When it is less than 0.03 g/m ² , the adhesiveness is lowered, and if it is thicker than 0.20 g/m ² , the anti-sticking property and the sliding property are not preferable.

In the present invention, the case where the low refractive index layer is provided may be provided in the same manner as the easy adhesion layer.

(polarizer)

The polarizing plate of the present invention is a polarizing plate having a polarizer protective film on both sides of the polarizer, and preferably at least one of the polarizer protective films is the easy-adhesive polyester film for protecting the polarizer. The other polarizer protective film may be the easy-adhesive polyester film for protecting the polarizer of the present invention, and the birefringence represented by the triethylenesulfonated cellulose film or the acrylic film or the norbornene-based film is also preferably used. The film is ideal.

Examples of the polarizer include those in which a polyvinyl alcohol-based film contains a dichroic material such as iodine. The polarizer protective film is bonded to the polarizer directly or via an adhesive layer. However, from the viewpoint of improving adhesion, it is preferred to bond it via an adhesive. At this time, the easy-adhesion layer of the present invention is preferably disposed on the polarizer surface or the adhesive layer. The preferred polarizer for the polyester film of the present invention is uniaxially stretched and maintained in an aqueous solution of boric acid by, for example, dyeing and adsorbing iodine or a dichroic material in a polyvinyl alcohol-based film. Washing in the extended state Obtained polarizer. The stretching ratio of the uniaxial stretching is usually about 4 to 8 times. Polyvinyl alcohol is suitable as a polyvinyl alcohol-based film, and it can be used as "KURARAYVINYLON" [Kuraray Co., Ltd.], "Tohcello VINYLON" [TOHCELLO (share) system", "Nikko VINYLON" [Japan Synthetic Chemicals Co., Ltd. )]] and other commercial products. Examples of the dichroic material include iodine, a disazo compound, a polymethine dye, and the like.

The adhesive applied to the polarizer is preferably a water-based one from the viewpoint of thinning the adhesive layer, that is, one in which the adhesive component is dissolved in water or dispersed in water. For example, a polyvinyl alcohol-based resin, a urethane resin, or the like can be used as a main component, and a composition such as an isocyanate compound or an epoxy compound may be blended as needed in order to improve adhesion. The thickness of the subsequent agent layer is preferably 10 μm or less, more preferably 5 μm or less, and still more preferably 3 μm or less.

In the case where a polyvinyl alcohol-based resin is used as a main component of the adhesive, in addition to partially saponified polyvinyl alcohol or fully saponified polyvinyl alcohol, a carboxyl group-modified polyvinyl alcohol or an ethylene-ethyl fluorene-modified polyethylene may be used. A modified polyvinyl alcohol-based resin of an alcohol, a hydroxymethyl-modified polyvinyl alcohol, or an amine-modified polyvinyl alcohol. The concentration of the polyvinyl alcohol-based resin in the subsequent agent is preferably from 1 to 10% by mass, more preferably from 2 to 7% by mass.

The polyester film for protecting a polarizer of the present invention is preferably used on the visible side of the visible side polarizing plate or the light source side of the light source side polarizing plate, and particularly when used on the light source side of the light source side polarizing plate, The brightness of the liquid crystal display device is improved and is preferred. When the polyester film for polarizer protection of the present invention is used as the light source side of the light source side polarizing plate, the light is incident from the side having a low average reflectance, and the liquid can be raised. The brightness of the crystal display device. Here, the "light source side" means the light source side in which the image display cell (for example, a liquid crystal cell) is used as a starting point among the two polarizing plates used in the image display device, and the "visible side" means The image shows the opposite side of the light source side as the starting point.

[Examples]

Next, the present invention will be described in detail using examples, comparative examples, and reference examples, but the present invention is of course not limited to the following examples. Further, the evaluation method used in the present invention is as follows.

(1) Glass transition temperature

According to JIS K7121, using a differential scanning calorimeter (made by Seiko Instruments Co., Ltd., DSC6200), 10 mg of the resin sample was heated at a temperature range of 25 to 300 ° C at 20 ° C / min, and the temperature at which the glass transition was obtained from the DSC curve was taken as Glass transfer temperature.

(2) number average molecular weight

0.03 g of the resin was dissolved in 10 ml of tetrahydrofuran, and a GPC-LALLS apparatus low-angle light scattering photometer LS-8000 (manufactured by Tosoh Corporation, tetrahydrofuran solvent, reference: polystyrene) was used, and a column temperature of 30 ° C and a flow rate of 1 ml were used. /min, column (shodex KF-802, 804, 806 manufactured by Showa Denko Co., Ltd.), and the number average molecular weight was measured.

(3) Resin composition

The resin was dissolved in dihydrochloroform, and subjected to 1H-NMR analysis using a nuclear magnetic resonance analyzer (NMR) Gemini-200 manufactured by Varian Co., Ltd., and the molar ratio of each composition was determined from the integral ratio thereof.

(4) Acid price

1 g (solid component) of the sample is dissolved in 30 ml of chloroform or dimethylformate The guanamine was titrated with a 0.1 N potassium hydroxide ethanol solution using phenolphthalein as an indicator, and the amount (mg) of KOH necessary for neutralizing the carboxyl group per 1 g of the sample was determined.

(5) Degree of saponification

According to JIS-K6726, sodium hydroxide was used to quantify the residual acetic acid group (mol%) of the polyvinyl alcohol resin, and this value was defined as the degree of saponification (% by mole). The same sample was measured 3 times, and the average value thereof was defined as the degree of saponification (% by mole).

(6) Total light transmittance of polyester film for polarizer protection

The total light transmittance of the polyester film for polarizer protection was measured in accordance with JIS K 7105 using a turbidimeter (manufactured by Nippon Denshoku Co., Ltd., NDH2000). Further, light was irradiated from the surface opposite to the surface of the polarizer protective film having an easy-to-attach layer and measured.

(7) Haze of polyester film for polarizer protection

The haze of the polarizer to protect the polyester film was measured in accordance with JIS K 7136 using a turbidimeter (manufactured by Nippon Denshoku Co., Ltd., NDH2000). Further, light was irradiated from the surface opposite to the surface of the polarizer protective film having an easy-to-attach layer and measured.

(8) PVA adhesion

On the surface of the easy-adhesive layer of the polyester film for polarizer protection, the thickness of the dried polyvinyl alcohol resin layer is set to 2 μm, and the polyvinyl alcohol aqueous solution (Coke is adjusted to have a solid content concentration of 5 mass% by wire bar coating) PVA117), dried at 70 ° C for 5 minutes. For the sake of easy determination, a red dye is added to an aqueous solution of polyvinyl alcohol. The film to be produced is a glass plate having a thickness of 5 mm to which a double-sided tape has been attached, and The opposite side of the surface of the laminated film on which the polyvinyl alcohol resin layer was formed of the evaluation target was attached to the above-mentioned double-sided tape. Next, a 100-square-shaped cut that penetrates the polyvinyl alcohol resin layer and reaches the base film is applied using a blade guide having a gap of 2 mm. Next, a sticky tape (slip tape (registered trademark) CT-24 manufactured by NICHIBAN Co., Ltd.; width 24 mm) was attached to a square-shaped cut surface. At the time of bonding, the air remaining in the interface was pressed by an eraser to completely close the air, and the operation of vertically peeling off the adhesive tape was performed once, five times, and ten times. The number of squares in which the polyvinyl alcohol resin layer was not peeled off was calculated and used as PVA adhesion. That is, in the case where the PVA layer was not peeled off completely, the PVA adhesion rate was set to 100, and the PVA layer was completely peeled off, and the PVA adhesion rate was set to be 0. In addition, there is a partial peeler in one square, which is also included in the number of stripped.

(9) Average reflectance

The method for measuring the average value of the absolute reflectance of the low-refractive-index layer of the laminated film for polarizer protection is attached to a black tape (Nitto Denko, plastic tape No. 21: black) attached to the back surface of the polyester film (easy adhesion layer) . Then, using a spectrophotometer (Shimadzu Corporation, UV-3150), the low refractive index was measured at an incident angle of 5°, a wavelength conversion speed: a high speed (about 700 nm/min), a sampling interval of 0.5 nm, and a spectral bandwidth of 1 nm. The surface of the layer has an absolute reflectance in the wavelength range of 300 to 800 nm, and an average value of 400 to 700 nm is calculated as an average refractive index.

(10) Refractive index of low refractive index layer

The refractive index of the low refractive index layer of the laminated polyester film for polarizer protection of the present invention is measured by the following method. The thickness after drying is set to about 4 μm, and the coating liquid for the low refractive index layer is coated on After the glass plate was dried and hardened, the value measured by an Abbe refractometer (manufactured by ATAGO, NAR-4T, measurement wavelength: 589 nm) was used as the refractive index of the low refractive index layer.

(polymerization of polyester resin)

In a stainless steel autoclave equipped with a stirrer, a thermometer, and a partial reflux cooler, 194.2 parts by mass of dimethyl terephthalate, 184.5 parts by mass of dimethyl isophthalate, and dimethyl-5-sulfonate were charged. 14.8 parts by mass of sodium isophthalate, 233.5 parts by mass of diethylene glycol, 136.6 parts by mass of ethylene glycol, and 0.2 parts by mass of tetra-n-butyl titanate, and esterification is carried out at a temperature of 160 ° C to 220 ° C for 4 hours. Exchange reactions. Then, the temperature was raised to 255 ° C, and the reaction system was gradually reduced in pressure, and then reacted under reduced pressure of 30 Pa for 1 hour and 30 minutes to obtain a copolymerized polyester resin (A-1). The obtained copolymerized polyester resin (A-1) was light yellow and transparent. The reducing viscosity of the copolymerized polyester resin (A-1) was measured and found to be 0.70 dl/g. The glass transition temperature measured by DSC was 40 °C.

In the same manner, copolymerized polyester resins (A-2) to (A-5) of other compositions were obtained. The composition (mol% ratio) and other characteristics measured by 1H-NMR for these copolymerized polyester resins are shown in Table 1.

(Preparation of polyester water dispersion)

In a reactor equipped with a stirrer, a thermometer, and a refluxing device, 30 parts by mass of a polyester resin (A-1) and 15 parts by mass of ethylene glycol n-butyl ether were charged, and the mixture was heated and stirred at 110 ° C to dissolve the resin. After the resin was completely dissolved, 55 parts by mass of water was slowly added to the polyester solution while stirring. After the addition, the liquid was stirred and cooled to room temperature to prepare a milky white polyester aqueous dispersion (Aw-1) having a solid content of 30% by mass. Similarly, a polyester resin (A-2) to (A-5) was used instead of the polyester resin (A-1) to prepare an aqueous dispersion, and each was designated as a polyester aqueous dispersion (Aw-2)~( Aw-5).

(Preparation of aqueous polyvinyl alcohol solution)

In a container equipped with a stirrer and a thermometer, 90 parts by mass of water was charged, and 10 parts by mass of a polyvinyl alcohol resin (manufactured by Kuraray) (B-1) having a polymerization degree of 500 was slowly added thereto while stirring. After the addition, the liquid was stirred and heated to 95 ° C to dissolve the resin. After dissolving, it is cooled to room temperature with stirring to obtain a solid. A 10% by mass aqueous solution of polyvinyl alcohol (Bw-1). Similarly, a polyvinyl alcohol resin (B-2) to (B-7) was used instead of the polyvinyl alcohol resin (B-1) to prepare an aqueous solution, which was designated as (Bw-2) to (Bw-7), respectively. . The degree of saponification of the polyvinyl alcohol resins (B-1) to (B-7) is shown in Table 2.

(polymerization of blocked polyisocyanate crosslinker)

In a flask equipped with a stirrer, a thermometer, and a reflux cooling tube, 100 parts by mass of a polyisocyanate compound having an isocyanurate structure (Duranate TPA, manufactured by Asahi Kasei Chemical Co., Ltd.) containing hexamethylene diisocyanate as a raw material, and propylene glycol monomethyl ether 55 parts by mass of acetate and 30 parts by mass of polyethylene glycol monomethyl ether (average molecular weight: 750) were kept at 70 ° C for 4 hours under a nitrogen atmosphere. Thereafter, the temperature of the reaction liquid was lowered to 50 ° C, and 47 parts by mass of methyl ethyl ketone oxime was added dropwise. The infrared spectrum of the reaction liquid was measured, and it was confirmed that the absorption of the isocyanate group disappeared, and a blocked polyisocyanate aqueous dispersion (C-1) having a solid content of 75% by mass was obtained.

(Synthesis of Polyurethane Resin D-1U)

A urethane resin D-1 having an aliphatic polycarbonate polyol as a constituent component was produced by the following procedure. In a four-necked flask equipped with a stirrer, a DIMROTH cooler, a nitrogen inlet tube, a silicone drying tube, and a thermometer, 43.75 parts by mass of 4,4-diphenylmethane diisocyanate and 12.85 parts by weight of dimethylolbutanoic acid were added. 153.11 parts by mass of polyhexamethylene carbonate diol having a molecular weight of 2000, 0.03 parts by mass of dibutyltin dilaurate, and 84.00 parts by mass of acetone as a solvent, and stirred at 75 ° C for 3 hours under a nitrogen atmosphere to confirm the reaction liquid. The established amine equivalent has been reached. Next, after the reaction liquid was cooled to 40 ° C, 8.77 parts by mass of triethylamine was added to obtain a polyurethane prepolymer solution. Then, 450 g of water was added to a reaction vessel equipped with a homogenizer capable of high-speed stirring, and the mixture was adjusted to 25° C., and the mixture was stirred and mixed at 2000 min ⁻¹ , and the polyurethane prepolymer solution was added thereto to carry out water dispersion. Thereafter, a water-soluble polyurethane resin having a solid content of 35% was prepared by removing a part of acetone and water under reduced pressure. The glass transition point temperature of the obtained polyurethane resin (D-1U) having an aliphatic polycarbonate polyol as a constituent component was -30 °C.

(Formation of low refractive index layer D-1)

The low refractive index layer coating liquid (D-1) was prepared in the following composition.

(cerium oxide sol having an average particle diameter of 100 nm, solid content concentration: 40% by mass), 0.60% by mass of surfactant (tantalum, solid content concentration: 10% by mass)

(Formation of low refractive index layer D-2)

The low refractive index layer coating liquid (D-2) was prepared in the following composition.

(RX2035A, Japan CARBIDE system, solid content 46%) (cerium oxide sol having an average particle diameter of 100 nm, solid content concentration: 40% by mass), 0.60% by mass of surfactant (tantalum, solid content concentration: 10% by mass)

(Formation of low refractive index layer D-3)

The low refractive index layer coating liquid (D-3) was prepared in the following composition.

(cerium oxide sol having an average particle diameter of 100 nm, solid content concentration: 40% by mass), 0.60% by mass of surfactant (tantalum, solid content concentration: 10% by mass)

(Formation of hard coating D-4)

The coating liquid for forming a hard coat layer of the following composition was applied to the surface of the polyester film produced in the examples described later on the opposite side to the surface of the polarizer, and dried at 70 ° C for 1 minute using a #10 wire bar. And remove the solvent. Next, the film coated with the hard coat layer was irradiated with ultraviolet rays of 300 mJ/cm ² using a high pressure mercury lamp to obtain a polarizer protective film having a hard coat layer having a thickness of 5 μm.

Hard coating layer forming coating liquid

(A-DPH of Shin-Nakamura Chemical Co., Ltd.) 6.80% by mass of polyethylene glycol diacrylate (A-400 manufactured by Shin-Nakamura Chemical Co., Ltd.) Photopolymerization initiator 1.00% by mass (Irgacure 184, manufactured by Ciba Specialty Chemicals Co., Ltd.)

(Formation of anti-glare layer D-5)

The coating liquid for forming an antiglare layer of the following composition was applied to the surface of the polyester film produced in the examples described later on the opposite side to the surface of the polarizer, and dried at 70 ° C for 1 minute using a #5 wire bar. And remove the solvent. Next, a film of the antiglare layer was irradiated with ultraviolet rays of 300 mJ/cm ² using a high pressure mercury lamp to obtain a polarizer protective film having an antiglare layer (D-5) having a thickness of 5 μm.

Coating liquid for forming an anti-glare layer

(Irgacure 184, manufactured by Ciba Specialty Chemicals)

(formation of anti-reflection layer D-6)

The coating film for forming a refractive index layer of the following composition was applied to the surface of the polyester film produced in the examples to be described later on the opposite side to the surface on the opposite side to the polarizer, and dried at 70 ° C for 1 minute. Thereafter, a high-pressure mercury lamp was used, and ultraviolet rays of 400 mJ/cm ^{2 were} irradiated to obtain a refractive index layer having a dry film thickness of 5 μm. Then, a coating liquid for forming a high refractive index layer having the following composition is formed on the intermediate refractive index layer by using a bar coater in the same manner as the medium refractive index layer, and a low refractive index layer of the following composition is formed. The coating liquid was formed thereon in the same manner as the medium refractive index layer, and the antireflection layer (D-6) was laminated to obtain a polyester film for polarizer protection.

Coating liquid for forming a medium refractive index layer (refractive index 1.52)

(Ciba Specialty Chemicals Co., Ltd., Irgacure 184) 100 parts by weight of isopropyl alcohol

Coating liquid for forming a high refractive index layer (refractive index 1.64)

Coating liquid for forming a low refractive index layer (refractive index 1.42)

Example 1

(1) Preparation of coating liquid for easy adhesion layer

The following coating agent was mixed to prepare a coating liquid having a polyester resin (A)/polyvinyl alcohol resin (B) in a mass ratio of 70/30. As the aqueous polyester dispersion, an aqueous dispersion (Aw-1) of a polyester resin having a dispersed acid value of 2 KOHmg/g was used, and an aqueous solution of polyvinyl alcohol having a degree of saponification of 74 mol% was used as an aqueous solution of the polyvinyl alcohol (Bw- 4).

(cerium oxide sol having an average particle diameter of 100 nm, solid content concentration of 40% by mass)

catalyst

(矽, solid concentration 10% by mass)

(2) Manufacture of polyester film for polarizer protection

As a film raw material polymer, a PET resin pellet having an intrinsic viscosity (solvent: phenol/tetrachloroethane = 60/40) of 0.62 dl/g and substantially free of particles was used at 135 ° C under a reduced pressure of 133 Pa. Dry for 6 hours. Thereafter, the mixture was supplied to an extruder, melt-extruded into a sheet shape at about 280 ° C, and rapidly cooled on a rotary cooling metal roll having a surface temperature of 20 ° C to be tightly cured to obtain an unstretched PET sheet.

The unstretched PET sheet was heated to 100 ° C by a heated roll group and an infrared heater, and then stretched 3.5 times in the longitudinal direction by a roll group having a circumferential speed difference to obtain a uniaxially stretched PET film.

Next, the coating liquid of the easy-adhesion layer and the coating liquid of the low refractive index layer D-1 were applied to both surfaces of the PET film by a roll coating method, and then dried at 80 ° C for 15 seconds. Further, the coating amount after the final (after biaxial stretching) drying was adjusted to 0.12 g/m ² . Then, it was extended to 4.0 times in the width direction at 150 ° C by a tenter, and heated at 230 ° C for 0.5 second in a state in which the length of the film was fixed in the width direction, and then relaxed in the width direction of 3% at 230 ° C. After treating for 10 seconds, a polyester film for polarizer protection having a thickness of 38 μm was obtained. The evaluation results are shown in Table 3.

Example 2

A polarizer protection was obtained in the same manner as in Example 1 except that the aqueous polyester dispersion of the easy-adhesion layer was changed to an aqueous dispersion (Aw-2) of a polyester resin having a dispersed acid value of 4 KOHmg/g. Use a polyester film.

Example 3

A polarizer protection was obtained in the same manner as in Example 1 except that the aqueous polyester dispersion of the easy-adhesion layer was changed to an aqueous dispersion (Aw-3) of a polyester resin having a dispersed acid value of 6 KOHmg/g. Use a polyester film.

Example 4

A polarizing plate protection was obtained in the same manner as in Example 1 except that the polyvinyl alcohol aqueous solution having an easily adhesive layer was changed to a polyvinyl alcohol aqueous solution (Bw-3) having a saponification degree of polyvinyl alcohol of 79 mol%. Polyester film.

Example 5

The saponification degree of the polyvinyl alcohol changed to the easy-adhesive layer was 83 m A polarizer-protected polyester film was obtained in the same manner as in Example 1 except for the aqueous polyvinyl alcohol solution (Bw-2).

Example 6

A polarizer was obtained in the same manner as in Example 1 except that the easy-to-adhere layer was changed to the following coating agent and the mass ratio of the polyester resin (A)/polyvinyl alcohol-based resin (B) was 60/40. Protective polyester film.

(cerium oxide sol having an average particle diameter of 100 nm, solid content concentration of 40% by mass)

catalyst

(矽, solid concentration 10% by mass)

Example 7

A polarizer was obtained in the same manner as in Example 1 except that the easy-adhesion layer was changed to the following coating agent and the mass ratio of the polyester resin (A)/polyvinyl alcohol resin (B) was 80/20. Protective polyester film.

(cerium oxide sol having an average particle diameter of 100 nm, solid content concentration of 40% by mass)

catalyst

(矽, solid concentration 10% by mass)

Example 8

In the same manner as in Example 1, except that the easy-to-adhere layer was changed to the following coating agent and the mass ratio of the polyester resin (A)/polyvinyl alcohol-based resin (B) was 50/50, polarized light was obtained. A polyester film for sheet protection.

(cerium oxide sol having an average particle diameter of 100 nm, solid content concentration of 40% by mass)

catalyst

(矽, solid concentration 10% by mass)

Example 9

A polyester film for protecting a polarizer was obtained in the same manner as in Example 1 except that the composition of the coating liquid of the easy-adhesion layer was changed as follows.

(NIKALAC MX-042 triad and chemical solid content concentration: 70%) particles 1.25 mass% (cerium oxide sol having an average particle diameter of 100 nm, solid content concentration: 40 mass%) 0.5% by mass of surfactant (lanthanum, solid content concentration) 10% by mass)

Example 10

A polarizing solution was obtained in the same manner as in Example 1 except that the polyvinyl alcohol aqueous solution of the easily-adherent layer was changed to an aqueous solution (Bw-5) of polyvinyl alcohol having a saponification degree of 70 mol% of dissolved polyvinyl alcohol. A polyester film for sheet protection.

Example 11

A polarizing solution was obtained in the same manner as in Example 1 except that the polyvinyl alcohol aqueous solution of the easily-adherent layer was changed to an aqueous solution (Bw-6) of polyvinyl alcohol having a saponification degree of 67 mol% of dissolved polyvinyl alcohol. A polyester film for sheet protection.

Example 12

A polyester film for protecting a polarizer was obtained in the same manner as in Example 1 except that the composition of the coating liquid of the easy-adhesion layer was changed to the following.

(EPOCROS WS-500, manufactured by Nippon Shokubai Co., Ltd., solid content concentration: 40% by mass) 1.25 mass% of particles (cerium oxide sol having an average particle diameter of 100 nm, solid content concentration: 40% by mass), 0.5% by mass of surfactant, Solid content concentration 10% by mass)

Example 13

A polarizer protection was obtained in the same manner as in Example 1 except that the aqueous polyester dispersion of the easy-adhesion layer was changed to an aqueous dispersion (Aw-5) of a polyester resin having a dispersed acid value of 10 KOHmg/g. Use a polyester film.

Example 14

A polyester film for protecting a polarizer was obtained in the same manner as in Example 1 except that the coating liquid of the low refractive index layer was changed to D-2.

Example 15

In addition to changing the coating liquid of the low refractive index layer to D-3, the system and implementation Example 1 was carried out in the same manner to obtain a polyester film for polarizer protection.

Example 16

A polyester film for protecting a polarizer was obtained in the same manner as in Example 1 except that D-4 was formed on the low refractive index layer D-1 of Example 1.

Example 17

A DME for protecting a polarizer was obtained in the same manner as in Example 1 except that D-5 was formed on the low refractive index layer D-1 of Example 1.

Example 18

A DIE for protecting a polarizer was obtained in the same manner as in Example 1 except that D-6 was formed on the low refractive index layer D-1 of Example 1.

Example 19

A polyester film for protecting a polarizer was obtained in the same manner as in Example 1 except that the film thickness of the low refractive index layer D-1 was changed to 0.06 g/m ² .

Example 20

A polyester film for protecting a polarizer was obtained in the same manner as in Example 1 except that the film thickness of the low refractive index layer D-1 was changed to 0.18 g/m ² .

Comparative example 1

The coating liquid of the easy-adhesion layer was changed in the same manner as in Example 1 except that the following coating agent was mixed and the mass ratio of the polyester resin (A)/polyvinyl alcohol resin (B) was changed to 100/0. A polyester film for protecting a polarizer is obtained.

1.25 mass% of particles (cerium oxide sol having an average particle diameter of 100 nm, solid content concentration of 40% by mass)

catalyst

(矽, solid concentration 10% by mass)

Comparative example 2

The coating liquid of the easy-adhesion layer was changed in the same manner as in Example 1 except that the following coating agent was mixed and the mass ratio of the polyester resin (A)/polyvinyl alcohol resin (B) was 0/100. A polyester film for protecting a polarizer is obtained.

(cerium oxide sol having an average particle diameter of 100 nm, solid content concentration of 40% by mass)

catalyst

(矽, solid concentration 10% by mass)

Comparative example 3

In addition to changing the polyester aqueous dispersion to a dispersed acid value of 25 KOHmg/g A polyester film for polarizer protection was obtained in the same manner as in Example 1 except that the aqueous dispersion of the polyester resin (Aw-4) was used.

Comparative example 4

A polyester film for protecting a polarizer was obtained in the same manner as in Example 1 except that the aqueous solution of polyvinyl alcohol was changed to an aqueous solution (Bw-1) of polyvinyl alcohol having a degree of saponification of 88 mol%.

Comparative Example 5

A polyester film for protecting a polarizer was obtained in the same manner as in Example 1 except that the polyvinyl alcohol aqueous solution was changed to an aqueous solution (Bw-7) of polyvinyl alcohol having a dissolved saponification degree of 40 mol%.

Comparative Example 6

A polyester film for protecting a polarizer was obtained in the same manner as in Example 1 except that the coating liquid of the easy-adhesion layer was changed to the following coating agent and the crosslinking agent was not mixed.

(cerium oxide sol having an average particle diameter of 100 nm, solid content concentration: 40% by mass) 0.5% by mass of surfactant (tantalum, solid content concentration: 10% by mass)

Comparative Example 7

The same as in the first embodiment except that the low refractive index layer is not provided. In the line, a polyester film for polarizer protection is obtained.

Comparative Example 8

A polyester film for protecting a polarizer was obtained in the same manner as in Example 1 except that the film thickness of the low refractive index layer D-1 was 0.02 g/m ² .

Reference example 1

A TAC film (manufactured by Fujifilm Co., Ltd., thickness: 80 μm, saponified) was used as a film for polarizer protection, and the results of the above-described adhesion test were shown.

[Industrial availability]

The easy-adhesive polyester film for polarizer protection of the present invention has high adhesion to a polarizer and a water-based adhesive, and has high transmittance, and can be suitably used as a polarizer protection member.

Claims (10)

A polyester film for protecting a polarizer, which is a polyester film having an easy-to-attach layer connected to a polarizer directly or via an adhesive layer on one side, the adhesive layer comprising a polyester resin (A) and The polyvinyl alcohol-based resin (B) and the crosslinking agent (C) have an acid value of 20 KOHmg/g or less, and the saponification degree of the polyvinyl alcohol-based resin (B) is 60 to 85 Ear %, the average absolute reflectance of light having a wavelength of 400 to 700 nm opposite to the one side of the polyester film is 6% or less. The polyester film for protecting a polarizer according to claim 1, wherein the opposite surface has a low refractive index layer having a lower refractive index than the polyester film. The polyester film for protecting a polarizer according to the second aspect of the invention, wherein the low refractive index layer is selected from at least one functional layer including a hard coat layer, an antiglare layer, and an antireflection layer. . The polyester film for protecting a polarizer according to any one of claims 1 to 3, wherein the polyester resin (A) contains 1 to 15 mol% of a 5-sulfo group in the dicarboxylic acid component. The isophthalic acid component. The polyester film for protecting a polarizer according to any one of claims 1 to 3, wherein the crosslinking agent (C) is an isocyanate compound or a melamine compound. The polyester film for protecting a polarizer according to the fourth aspect of the invention, wherein the crosslinking agent (C) is an isocyanate compound or a melamine compound. Polarizer protection for use in any of claims 1 to 3 An ester film in which the mass ratio of the polyester resin (A), the polyvinyl alcohol resin (B), and the crosslinking agent (C) simultaneously satisfies the following formula; 0.8 ≦ (A) / ( B) ≦5 2≦((A)+(B))/(C)≦50. The polyester film for protecting a polarizer according to item 4 of the patent application, wherein the mass ratio of the polyester resin (A), the polyvinyl alcohol resin (B), and the crosslinking agent (C) in the easy-adhesion layer The system satisfies the following formula; 0.8 ≦ (A) / (B) ≦ 5 2 ≦ ((A) + (B)) / (C) ≦ 50. A polarizing plate is a polarizing plate having a polarizer protective film on both sides of a polarizer, and at least one of the polarizer protective films is a polarizer protective polyester according to any one of claims 1 to 8. film. An image display device having at least one polarizing plate as in claim 9 of the patent application.