JP2013033098A - Antiglare film and method for manufacturing antiglare film - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide an antiglare film having excellent antiglare property, giving sharpness in black and image display with high contrast when the antiglare film is used in an image display device, and having high hardness, a good surface state while suppressing an uneven cured state, and excellent handling property, and to provide a method for manufacturing the antiglare film.SOLUTION: The antiglare film comprises a transparent support having a thickness of 30 to 65 μm and an antiglare layer having a thickness of 2.0 to 5.0 μm formed on the support. The antiglare layer includes: a crosslinked acrylic resin comprising a crosslinked acrylic compound having at least an average acryl equivalent of 100 or less; and light-transmitting particles having an average particle diameter of 1.0 to 3.0 μm. The antiglare film shows a haze value of 0.5 to 3.0% and an absolute curvature of 0 to 18/m in terms of a largest curl under the conditions of 25°C and 60% RH.

Description

  The present invention relates to an antiglare film and a method for producing the antiglare film.

In recent years, display devices are used at home, and toughness is required for handling of general users. Various image display devices such as liquid crystal display (LCD), plasma display panel (PDP), electroluminescence display (ELD), cathode ray tube display (CRT), SED (Surface-Conduction Electron-emitter Display) The optical film used on the surface is required to have high physical strength (such as scratch resistance), transparency, chemical resistance, and weather resistance (such as moisture and heat resistance). Further, in order to prevent a decrease in contrast due to reflection of external light or reflection of an image, antiglare performance and antireflection performance are required.
In addition, with the thinning of the display device, there is a strong demand for thinning each member, and a film of 70 μm or less is strongly demanded for the antiglare film. However, when the antiglare film is made 70 μm or less, there is a problem that physical strength deteriorates.

  In order to secure physical strength, a cured layer using a (meth) acrylate resin such as DPHA (dipentaerythritol hexaacrylate) or PETA (pentaerythritol triacrylate) is provided on the film support as a material exhibiting high hardness. However, optical films with such a hardened layer are difficult to handle during manufacturing and processing due to strong curling, and may peel off after being bonded to other members. May occur. In order to improve these, the thickness of the cured layer is reduced (for example, see Patent Document 1), modified acrylate compounds (for example, see Patent Documents 2 and 3), urethane acrylate compounds (for example, see Patent Document 4) ), Acrylate compounds having different properties (for example, see Patent Documents 5 and 6) and the like are disclosed.

JP 2006-276839 A JP 2005-181996 A JP 2005-275391 A JP 2007-256844 A JP 2005-103979 A JP 2003-335983 A

However, in the inventions described in Patent Documents 1 to 6, although the curl improving effect and the improvement in brittleness are recognized, the film surface hardness itself is lowered, and it is difficult to achieve both the surface hardness and these properties. there were.
Further, in order to obtain an image display with black tightening, the antiglare film is required to have low haze. However, in the antiglare film having low haze, the transparent support is deformed due to curing shrinkage of the antiglare layer. The problem was that scattering unevenness (curing unevenness) of generated reflected light was large. This unevenness of curing is hardly visually recognized in a clear film having no antiglare property (having a haze of almost 0%) or a high haze antiglare film having a haze of 10% or more. On the other hand, in the anti-glare film having a low haze, the visibility of curing unevenness was increased and the quality was lowered. In addition, thinning of the panel and thinning of the antiglare film have been desired. However, as the thickness of the transparent support is reduced, the base material is likely to be deformed and unevenness is worsened, so improvement is desired. It was.

  An object of the present invention is excellent in antiglare properties, provides an image display with black tightening when used in an image display device, has high hardness, suppresses unevenness of curing, has a good surface shape, and has excellent handleability. It is providing the anti-glare film and its manufacturing method. Furthermore, the objective of this invention is providing the polarizing plate and image display apparatus which used this anti-glare film.

  As a result of intensive studies to solve the above-mentioned problems, the present inventors have completed the present invention by adopting the following configuration. That is, the present invention has the following configuration.

[1]
An antiglare film having an antiglare layer having a thickness of 2.0 to 5.0 μm on a transparent support having a thickness of 30 to 65 μm,
The antiglare layer has a crosslinked acrylic resin in which an acrylic compound having an average acrylic equivalent of 100 or less is cross-linked, and translucent particles having an average particle diameter of 1.0 to 3.0 μm,
The anti-glare film whose haze value of this anti-glare film is 0.5-3.0%, and the absolute value of the curvature of the maximum curl under 25 degreeC60% RH is 0-18 / m.
[2]
The antiglare film according to [1], wherein the absolute value of the curvature of the maximum curl at 25 ° C. and 60% RH of the antiglare film is 0 to 8 / m.
[3]
The antiglare film according to [1] or [2], wherein the transparent support is a cellulose ester film containing an esterified compound of a compound having at least one furanose structure or at least one pyranose structure.
[4]
The antiglare film according to any one of [1] to [3], further including a low refractive index layer having a lower refractive index than the antiglare layer on the antiglare layer.
[5]
The polarizing plate which used the anti-glare film as described in any one of [1]-[4] for at least one of the protective films of a polarizing film.
[6]
The image display apparatus with which the anti-glare film as described in any one of [1]-[4], or the polarizing plate as described in [5] was arrange | positioned on the image display surface.
[7]
A method for producing an antiglare film having an antiglare layer having a thickness of 2.0 to 5.0 μm on a transparent support having a thickness of 30 to 65 μm,
A curable composition containing the following (A) to (D) and having a solid content ratio of 20 to 40% by mass is applied on the transparent support by 15 to 25 cc / m ² to form a coating film, and then the coating film is irradiated with ultraviolet rays. A method for producing an antiglare film, wherein the antiglare layer is formed by irradiating and curing.
(A) Acrylic compound having an average acrylic equivalent of 100 or less (B) 3 to 15 parts by mass (C) of translucent particles having an average particle diameter of 1.0 to 3.0 μm with respect to 100 parts by mass of the acrylic compound The α-aminoalkylphenone photopolymerization initiator is used in an amount of 0.5 to 5 parts by mass (D) organic solvent [8] based on 100 parts by mass of the acrylic compound.
The production of the antiglare film according to [7], wherein the (C) α-aminoalkylphenone photopolymerization initiator is 2-methyl-1- (4-methylthiophenyl) -2-morpholinopropan-1-one. Method.
[9]
In the ultraviolet irradiation process, the transparent support is wound around a backup roll having a diameter of 400 mm or less, the tension applied in the transport direction of the transparent support is 400 N / m or more, and the film surface temperature of the coating film is 25 ° C. In the following conditions, ultraviolet irradiation is performed by at least three or more ultraviolet irradiation devices, and the peak illumination intensity of ultraviolet irradiation of the first lamp and the second lamp is 5 to 50 mW / cm ² , respectively. The manufacturing method of the anti-glare film as described in [8] whose total of the irradiation amount of the ultraviolet-ray by an apparatus is 100 mJ / cm < ² > or more.

  According to the present invention, an image display with excellent antiglare property, black tightening when used in an image display device is obtained, high hardness, curling unevenness is suppressed, surface shape is good, and handleability is excellent. An antiglare film can be obtained.

In the manufacturing method of the anti-glare film of this invention, it is a schematic diagram which shows an example which irradiates with an ultraviolet-ray with the ultraviolet irradiation device of 3 or more lamps.

  Hereinafter, although the form for implementing this invention is demonstrated in detail, this invention is not limited to these. In the present specification, when numerical values represent physical property values, characteristic values, etc., the description “(numerical value 1) to (numerical value 2)” is “(numerical value 1) or more (numerical value 2) unless otherwise specified. ) "Means below. In the present specification, the description “(meth) acrylate” means “at least one of acrylate and methacrylate”. The same applies to “(meth) acrylic acid”, “(meth) acryloyl” and the like.

[Anti-glare film]
The antiglare film of the present invention is an antiglare film having an antiglare layer having a thickness of 2.0 to 5.0 μm on a transparent support having a thickness of 30 to 65 μm, and the antiglare layer is at least an average acrylic. It has a cross-linked acrylic resin cross-linked with a cross-linkable acrylic compound having an equivalent weight of 100 or less, and translucent resin particles having an average particle size of 1.0 to 3.0 μm, and the antiglare film has a haze value of 0.5 to 0.5. The absolute value of the curvature of the maximum curl at 3% and 25 ° C. and 60% RH is 0 to 18 / m. With such a configuration, the antiglare property is excellent, the black tightening property is good (image display with black tightening is obtained when used in an image display device), the hardness is high, and there is no unevenness in curing, and the surface shape is good. An antiglare film can be obtained.

In order to realize a high hardness antiglare layer, it is generally known that it is effective to increase the crosslink density of the film of the antiglare layer and to increase the film thickness. However, when aiming to increase the hardness of the antiglare layer by these methods, there is a problem that the transparent support is deformed by curing shrinkage at the time of film curing, curling occurs, or unevenness of curing occurs and the surface condition deteriorates. It was.
On the other hand, in the present invention, the hardness of the antiglare layer is designed to be 2.0 to 5.0 μm, and a high hardness is obtained by using a crosslinked acrylic resin crosslinked with a crosslinkable acrylic compound having an average acrylic equivalent of 100 or less. It was found that an antiglare film having a good surface condition can be obtained. Preferably, when the crosslinkable acrylic compound is crosslinked, by using an α-aminoalkylphenone photopolymerization initiator, the polymerization rate on the side far from the transparent support in the antiglare layer is high, and the transparent support It is possible to design a low polymerization rate on the side close to. When the antiglare layer has such a polymerization rate distribution, it is possible to suppress the curing shrinkage stress from being transmitted to the transparent support, to achieve both high hardness and good surface condition, and to further reduce curl.

  In the antiglare film of the present invention, the film thickness of the antiglare layer is 2.0 to 5.0 μm, preferably 2.5 to 4.5 μm. By setting the film thickness of the antiglare layer within this range, the surface shape is good, the load such as drying is small, and high productivity can be maintained.

In the antiglare film of the present invention, the absolute value of the curvature of the maximum curl at 25 ° C. and 60% RH is 0 to 18 / m, and preferably 0 to 8 / m. The smaller this value, the smaller the curl. Although it is preferable that the absolute value of the curvature of the maximum curl is small, designing in this range facilitates handling in manufacturing and processing.
The absolute value of the maximum curl was measured by the template method for curl measurement of Method A in “Measuring Method of Curling of Photographic Film” of JIS-K7619-1988.
The measurement conditions are 25 ° C., relative humidity 60%, humidity control time 5 hours, and are the values when curl is expressed by the following mathematical formula.
(Formula) Curl = 1 / R R is the radius of curvature (m)

In the antiglare film of the present invention, the haze value (total haze value) is 0.5 to 3%, preferably 0.7 to 2%. By setting the haze value within this range, it is possible to achieve both excellent antiglare property and black tightening property when applied to an image display device.
Here, the measurement of the total haze value of the antiglare film can be performed as follows.
That is, the total haze value (H) of the obtained antiglare film is measured according to JIS-K7136. As a measuring device, Nippon Denshoku Industries Co., Ltd. haze meter NDH2000 can be used.

Hereinafter, each component which comprises an anti-glare layer, each component used for the curable composition used for forming this anti-glare layer, etc. are demonstrated.
(A) Crosslinked acrylic resin The antiglare layer in the antiglare film of the present invention contains a crosslinked acrylic resin in which an acrylic compound having an average acrylic equivalent of 100 or less is crosslinked in order to achieve high hardness.
Here, “acryl equivalent” means the molecular weight per (meth) acryloyl group in the compound. “Average acrylic equivalent” means a mass average value of acrylic equivalents.
The crosslinked acrylic resin may be a resin obtained by crosslinking an acrylic compound having an acrylic equivalent of 100 or less alone, or may be a resin obtained from a plurality of types of acrylic compounds. When using a plurality of types of acrylic compounds, an acrylic compound having an acrylic equivalent of 100 or less and an acrylic compound having an acrylic equivalent of more than 100 may be mixed and used. In that case, the mass average value of the acrylic equivalent is 100 or less.
By using an acrylic compound having an average acrylic equivalent of 100 or less, the crosslink density of the antiglare layer is increased and high hardness can be realized. The average acrylic equivalent of the acrylic compound used in the present invention is preferably 99 or less, and more preferably 97 or less. The lower limit is preferably 85 or more.

Examples of the acrylic compound having an acrylic equivalent of 100 or less include trimethylolpropane triacrylate, pentaerythritol triacrylate, pentaerythritol tetraacrylate, dipentaerythritol hexaacrylate, and the like. Among them, dipentaerythritol hexaacrylate is preferably used from the viewpoint of reducing the penetration into the transparent support and improving the hardness.
As the acrylic compound having an acrylic equivalent exceeding 100 that can be used in combination with the acrylic compound, a monomer having two or more ethylenically unsaturated groups is preferable. As the monomer, ester of polyhydric alcohol and (meth) acrylic acid {for example, ethylene glycol di (meth) acrylate, 1,4-cyclohexane diacrylate, 1,2,3-chlorohexane tetramethacrylate, polyurethane acrylate} , Vinylbenzene and derivatives thereof (for example, 1,4-divinylbenzene, 4-vinylbenzoic acid-2-acryloylethyl ester, 1,4-divinylcyclohexanone), vinyl sulfone (for example, divinyl sulfone), (meth) acrylamide ( For example, methylenebisacrylamide) and the like can be mentioned. Among these, polyurethane acrylate is preferable from the balance of hardness and curl. A commercially available polyurethane acrylate compound can also be used, and UV7640B (manufactured by Nippon Synthetic Chemical), UV1700B (manufactured by Nippon Synthetic Chemical), UA306H (manufactured by Kyoeisha Chemical), UA306I (manufactured by Kyoeisha Chemical), U-4HA (manufactured by Kyoeisha Chemical) Shin-Nakamura Chemical Co., Ltd.) is preferably used.

In the present invention, the antiglare layer is formed by curing the curable composition containing an acrylic compound having an acrylic equivalent of 100 or less (that is, the acrylic compound is crosslinked to form a crosslinked acrylic resin). preferable.
Although content of the acrylic compound whose acrylic equivalent in a curable composition is 100 or less is not specifically limited, When the whole composition is 100 mass parts, 75-95 mass parts is preferable, and 80-92 mass parts is more. preferable.

(B) Translucent Particle The antiglare layer in the antiglare film of the present invention contains at least one translucent particle having an average particle diameter of 1.0 to 3.0 μm. The average particle diameter of the translucent particles is preferably 1.5 μm to 2.5 μm. By setting the average particle diameter of the translucent particles to 1 μm or more, an excellent antiglare property can be obtained. Moreover, even in a thin-film antiglare layer having a film thickness of 2.0 to 5.0 μm by making the average particle size 3 μm or less, the surface roughness is suppressed, and when applied to an image display device, black tightening is prevented. A certain display image can be obtained.
The value obtained by dividing the film thickness by the average particle diameter is preferably 1.2 to 3.5, more preferably 1.5 to 2.8. By setting the film thickness / average particle diameter to a value within this range, it is possible to reduce defects due to coarse particles that are excellent in antiglare properties and surface roughness and that are generated in the particle synthesis process.
The translucent particles may be either organic particles (resin particles) or inorganic particles, and may be used in combination. However, the refractive index can be easily controlled, and organic particles are preferable from the viewpoint of miniaturization of irregularities.
As a means for adjusting the surface shape, it is also preferable to use two or more kinds of particles having different average particle diameters or two or more kinds of particles having different refractive indexes.

Any measuring method can be applied to the method for measuring the particle size of the translucent particles as long as the particle size of the particles is measured. However, the particle size distribution of the particles is measured by a Coulter counter method, and the measured distribution is calculated. Particles are observed with a method of calculating from a particle distribution obtained by converting to a particle number distribution or a transmission electron microscope (magnification of 500,000 to 2,000,000 times), and 100 particles are observed. There is a method of making the particle size.
In the present invention, the average particle diameter is a value obtained by the Coulter counter method.

  Examples of the inorganic particles include aggregated metal oxide particles. Moreover, in the case of use, it can be used 1 type or in mixture of 2 or more types. Aggregated metal oxide particles are particularly preferably agglomerated silica particles and agglomerated alumina particles. Among them, agglomerated silica in which particles having a primary particle diameter of several tens of nanometers form an aggregate, This is preferable in that moderate surface irregularities can be stably formed. Agglomerated silica can be obtained, for example, by a so-called wet method synthesized by a neutralization reaction between sodium silicate and sulfuric acid, but is not limited thereto. The wet method is further roughly classified into a sedimentation method and a gelation method, and the present invention may be any method.

  When the translucent particles are resin particles (hereinafter also referred to as translucent resin particles), the refractive index thereof is different from any refractive index selected from methylene iodide, 1,2-dibromopropane, and n-hexane. Measure turbidity by dispersing equal amounts of translucent resin particles in a solvent whose refractive index is changed by changing the mixing ratio of the types of solvents, and determine the refractive index of the solvent when the turbidity is minimized. It is measured by measuring with an Abbe refractometer.

  The translucent resin particles can also impart internal scattering properties by controlling the difference in refractive index from the binder (for example, cross-linked acrylic resin). However, if the refractive index difference is excessively increased, the contrast is lowered. Therefore, the difference from the refractive index of the antiglare layer excluding the translucent resin particles is preferably designed to be 0.050 or less, more preferably 0.020 or less, and most preferably 0.010 or less. By designing in this region, a high contrast can be obtained. In addition, when using 2 or more types of translucent resin particles in this invention, a refractive index may be the same or may differ.

  Specific examples of the translucent resin particles include, for example, crosslinked polymethyl methacrylate particles, crosslinked polyethyl methacrylate particles, crosslinked polybutyl methacrylate particles, crosslinked polypropyl methacrylate particles, and crosslinked methyl methacrylate-styrene copolymer particles. And resin particles such as crosslinked polystyrene particles, crosslinked methyl methacrylate-methyl acrylate copolymer particles, crosslinked acrylate-styrene copolymer particles, melamine / formaldehyde resin particles, and benzoguanamine / formaldehyde resin particles. Of these, crosslinked styrene particles, crosslinked polymethyl methacrylate particles, crosslinked polyethyl methacrylate particles, crosslinked polybutyl methacrylate particles, and crosslinked methyl methacrylate-styrene copolymer particles are preferred. Furthermore, the surface of these resin particles is surface-modified particles in which a compound containing fluorine atom, silicon atom, carboxyl group, hydroxyl group, amino group, sulfonic acid group, phosphoric acid group or the like is chemically bonded, or nano-sized such as silica or zirconia. Examples of the particles include inorganic fine particles bonded to the surface.

The translucent particles used in the present invention may be one type or two or more types.
Moreover, in this invention, the curable composition used for forming an anti-glare layer is made to contain at least 1 sort of translucent particle | grains whose said average particle diameter is 1.0-3.0 micrometers. The content of the translucent particles in the curable composition is preferably 3 to 15 parts by mass with respect to 100 parts by mass of the acrylic compound from the viewpoint of achieving both antiglare properties and black tightening properties. It is more preferably 12 parts by mass.

(C) Polymerization initiator Polymerization of the acrylic compound in the present invention can be performed by irradiation with ionizing radiation or heating in the presence of a photoradical polymerization initiator or a thermal radical polymerization initiator.
Therefore, a curable composition containing the acrylic compound, translucent particles, radical photopolymerization initiator or thermal radical polymerization initiator, organic solvent, and if necessary, an inorganic filler, coating aid, other additives, etc. It is preferable that an antiglare layer is formed by preparing a product (coating solution) and coating the composition on a transparent support, followed by curing by a polymerization reaction with ionizing radiation or heat. More preferably, the curable composition is a radical polymerization initiator, and the composition is cured by irradiation with ultraviolet rays to form an antiglare layer.
It is also preferable to perform ionizing radiation curing and heat curing together. Commercially available compounds can be used as the photo- and thermal radical polymerization initiators, and they are described in “Latest UV Curing Technology” (p.159, publisher; Kazuhiro Takahisa, publisher; Technical Information Association, Inc.). 1991) and Ciba Specialty Chemicals catalog. Two or more photopolymerization initiators can be used in combination.
The radical photopolymerization initiator is 0.5 to 5 parts by mass in total with respect to 100 parts by mass of the acrylic compound in the curable composition for forming the antiglare layer, from the viewpoint of securing hardness and suppressing curing unevenness. It is preferable to use in the range, and more preferable to use in the range of 1 to 4 parts by mass.

In the present invention, it is preferable to contain at least an α-aminoalkylphenone photopolymerization initiator as a photoradical polymerization initiator. Since the α-aminoalkylphenone photopolymerization initiator has a very high reactivity and the surface curability of the coating film is high, the polymerization rate on the side far from the transparent support in the coating film is high, and the transparent support It is possible to design a low polymerization rate on the side close to. For this reason, it becomes difficult for the shrinkage stress generated at the time of film hardening to be transmitted to the transparent support, and uneven curing can be reduced. Further, excellent surface hardness can be obtained.
As the α-aminoalkylphenone photopolymerization initiator, 2-methyl-1- (4-methylthiophenyl) -2-morpholinopropan-1-one, 2-benzyl-2-dimethylamino-1- (4- Morpholinophenyl) -butanone, 1,2- (dimethylamino) -2-[(4-methylphenyl) methyl] -1- [4- (4-morpholinyl) phenyl] -1-butanone, and the like. Of these, 2-methyl-1- (4-methylthiophenyl) -2-morpholinopropan-1-one is preferable.

Preferable examples of commercially available radical photopolymerization initiators include Irgacure 907, 369, and 379 manufactured by BASF, and combinations thereof. Among these, Irgacure 907 is preferable.
The α-aminoalkylphenone photopolymerization initiator used in the present invention may be one type or two or more types.

[Organic polymer thickener]
The curable composition for forming the antiglare layer in the present invention may contain an organic polymer thickener.
The term “thickener” as used herein means that the viscosity of the composition is increased by adding it, and the magnitude of increase in the viscosity of the composition by adding is preferably 0.5 to 50 mPa. · S, more preferably 1 to 5 mPa · s.

  In the present invention, a cellulose ester is preferred as the organic polymer thickener. Among these, cellulose acetate butyrate is particularly preferable. The following are mentioned as an example of an organic polymer thickener including these.

Poly-ε-caprolactone poly-ε-caprolactone diol poly-ε-caprolactone triol polyvinyl acetate poly (ethylene adipate)
Poly (1,4-butylene adipate)
Poly (1,4-butylene glutarate)
Poly (1,4-butylene succinate)
Poly (1,4-butylene terephthalate)
polyethylene terephthalate)
Poly (2-methyl-1,3-propylene adipate)
Poly (2-methyl-1,3-propylene glutarate)
Poly (neopentyl glycol adipate)
Poly (neopentyl glycol sebacate)
Poly (1,3-propylene adipate)
Poly (1,3-propylene glutarate)
Polyvinyl butyral polyvinyl formal polyvinyl acetal polyvinyl propanal polyvinyl hexanal polyvinyl pyrrolidone polyacrylic acid ester polymethacrylic acid ester cellulose acetate cellulose propionate cellulose acetate butyrate

The molecular weight of the organic polymer thickener is preferably from 30,000 to 400,000 in terms of number average molecular weight, more preferably from 4,000 to 300,000, particularly preferably from 50,000 to 200,000.
The addition amount of the organic polymer thickener is preferably 0.2 to 10% by mass, and preferably 0.5 to 5.0% by mass with respect to the total solid content of the curable composition for forming the antiglare layer. More preferred.

[Surfactant]
In the curable composition for forming the antiglare layer in the present invention, in order to ensure surface uniformity such as coating unevenness, drying unevenness, point defects, etc., any surface activity of fluorine or silicone It is preferable to contain an agent or both. In particular, a fluorine-based surfactant can be preferably used because an effect of improving surface defects such as coating unevenness, drying unevenness, and point defects appears at a smaller addition amount. Productivity can be improved by giving high-speed coating suitability while improving surface uniformity.

Preferable examples of the fluorosurfactant include a fluoroaliphatic group-containing copolymer (hereinafter sometimes abbreviated as “fluorine polymer”).
As the fluoropolymer,
An acrylic resin or a methacrylic resin containing a repeating unit derived from the monomer (i) below, or a copolymer of the repeating unit and a vinyl monomer copolymerizable therewith, or
An acrylic resin or a methacrylic resin containing a repeating unit derived from the monomer (i) below and a repeating unit derived from the monomer (ii) below, or a vinyl monomer copolymerizable with these repeating units A copolymer is mentioned.

(I) Fluoroaliphatic group-containing monomer represented by the following general formula A

In the general formula A, R ¹¹ represents a hydrogen atom or a methyl group, X represents an oxygen atom, a sulfur atom or —N (R ¹² ) —, m represents an integer of 1 to 6, and n represents an integer of 2 to 4. . R ¹² represents a hydrogen atom or an alkyl group having 1 to 4 carbon atoms, specifically a methyl group, an ethyl group, a propyl group or a butyl group, preferably a hydrogen atom or a methyl group. X is preferably an oxygen atom.

(Ii) Monomer represented by the following general formula (b) copolymerizable with the above (i)

In General Formula B, R ¹³ represents a hydrogen atom or a methyl group, Y represents an oxygen atom, a sulfur atom or —N (R ¹⁵ ) —, R ¹⁵ represents a hydrogen atom or an alkyl group having 1 to 4 carbon atoms, specifically Specifically, it represents a methyl group, an ethyl group, a propyl group or a butyl group, preferably a hydrogen atom or a methyl group. Y is preferably an oxygen atom, —N (H) —, or —N (CH ₃ ) —.
R ¹⁴ represents a linear, branched or cyclic alkyl group having 4 to 20 carbon atoms which may have a substituent. Examples of the substituent for the alkyl group represented by R ¹⁴ include a hydroxyl group, an alkylcarbonyl group, an arylcarbonyl group, a carboxyl group, an alkyl ether group, an aryl ether group, a halogen atom such as a fluorine atom, a chlorine atom, and a bromine atom, a nitro group, and a cyano group. , Amino groups and the like, but not limited thereto. Examples of the linear, branched or cyclic alkyl group having 4 to 20 carbon atoms include a butyl group, pentyl group, hexyl group, heptyl group, octyl group, nonyl group, decyl group and undecyl group which may be linear or branched. , Dodecyl group, tridecyl group, tetradecyl group, pentadecyl group, octadecyl group, eicosanyl group, etc., and monocyclic cycloalkyl groups such as cyclohexyl group, cycloheptyl group and bicycloheptyl group, bicyclodecyl group, tricycloundecyl group, A polycyclic cycloalkyl group such as a tetracyclododecyl group, an adamantyl group, a norbornyl group, a tetracyclodecyl group, or the like is preferably used.

  The amount of the fluoroaliphatic group-containing monomer represented by the general formula A used in the fluorine-based polymer used in the present invention is 10 mol% or more based on each monomer of the fluorine-based polymer, preferably It is 15-70 mol%, More preferably, it is the range of 20-60 mol%.

The preferred weight average molecular weight of the fluoropolymer used in the present invention is preferably 3000 to 100,000, more preferably 5,000 to 80,000.
Furthermore, the preferable addition amount of the fluoropolymer used in the present invention is in the range of 0.001 to 5 parts by mass, more preferably in the range of 0.005 to 3 parts by mass with respect to 100 parts by mass of the curable composition. More preferably, it is the range of 0.01-1 mass part. If the addition amount of the fluorine-based polymer is 0.001 part by mass or more, the effect of adding the fluorine-based polymer is sufficiently obtained, and if the addition amount is 5 parts by mass or less, the coating film cannot be sufficiently dried or applied. There is no problem of adversely affecting the performance as a film (for example, reflectance, scratch resistance).

[Organic solvent]
As the organic solvent used in the curable composition for forming each layer of the antiglare film of the present invention, each component can be dissolved or dispersed, and it is easy to form a uniform surface in the coating process and the drying process. Various solvents selected from the viewpoints of ensuring liquid storage stability and having an appropriate saturated vapor pressure can be used.
Two or more kinds of solvents can be mixed and used.
In the curable composition for forming the antiglare layer of the present invention, in order to ensure the adhesion between the transparent support and the coating film, a solvent having a boiling point of 80 ° C. or lower is 5 to 5% in all the solvents of the curable composition. It is preferable to contain 50 mass%, and it is still more preferable to contain 10-30 mass%. Soaking can be controlled by the amount of solvent having a boiling point of 80 ° C. or less. By controlling the penetration of the resin component into the transparent support, both good adhesion and hardness can be achieved.
As another solvent, it is preferable to contain a solvent having a boiling point of more than 100 ° C. in order to adjust the drying speed.

  Examples of the solvent having a boiling point of 80 ° C. or lower include hydrocarbons such as hexane (boiling point 68.7 ° C.), dichloromethane (39.8 ° C.), chloroform (61.2 ° C.), carbon tetrachloride (76.8). Halogenated hydrocarbons, such as diethyl ether (34.6 ° C), diisopropyl ether (68.5 ° C), tetrahydrofuran (66 ° C), ethyl formate (54.2 ° C), methyl acetate ( Esters such as ethyl acetate (77.1 ° C.), ketones such as acetone (56.1 ° C.), 2-butanone (same as methyl ethyl ketone, 79.6 ° C.), methanol (64. 5 ° C) and ethanol (78.3 ° C), carbon disulfide (46.2 ° C), and the like. Of these, ketones and esters are preferable, and ketones are particularly preferable. Among the ketones, 2-butanone is particularly preferable.

  Examples of the solvent having a boiling point exceeding 100 ° C. include octane (125.7 ° C.), toluene (110.6 ° C.), xylene (138 ° C.), tetrachloroethylene (121.2 ° C.), chlorobenzene (131.7 ° C.), Dioxane (101.3 ° C.), dibutyl ether (142.4 ° C.), isobutyl acetate (118 ° C.), cyclohexanone (155.7 ° C.), 2-methyl-4-pentanone (same as MIBK, 115.9 ° C.), Examples thereof include 1-butanol (117.7 ° C.), N, N-dimethylformamide (153 ° C.), N, N-dimethylacetamide (166 ° C.), dimethyl sulfoxide (189 ° C.) and the like. Cyclohexanone and 2-methyl-4-pentanone are preferable.

  Moreover, in order to control the cohesiveness of translucent particle | grains, it is preferable to contain 20-80 mass% of solvents with SP value of 23 or more in all the solvents. By setting the SP value within this range, it is possible to promote aggregation of the light-transmitting particles and realize excellent antiglare property and black tightening property. Examples of the solvent having an SP value of 23 or more include methanol, ethanol, 1-propanol, 2-propanol, 1-butanol and the like. Of these, 2-propanol is preferable.

  In the curable composition for forming the antiglare layer, the content of the organic solvent is preferably 150 to 400 parts by mass, and 200 to 350 parts by mass with respect to 100 parts by mass of the composition. Is more preferable.

[Inorganic filler]
In addition to the above light-transmitting particles, the antiglare layer of the present invention can be used for adjusting the refractive index, adjusting the film strength, reducing curing shrinkage, and reducing the reflectance when a low refractive index layer is provided. Inorganic fillers can also be used. For example, it is composed of an oxide containing at least one metal element selected from titanium, zirconium, aluminum, indium, zinc, tin, and antimony, and the average particle diameter of primary particles is generally 0.2 μm or less, preferably It is also preferable to contain a fine high refractive index inorganic filler that is 0.1 μm or less, more preferably 0.06 μm or less and 1 nm or more.
When it is necessary to lower the refractive index of the matrix in order to adjust the difference in refractive index with the light-transmitting particles, a fine low refractive index inorganic filler such as silica fine particles or hollow silica fine particles is used as the inorganic filler. be able to. The preferred particle size is the same as that of the fine high refractive index inorganic filler.
The surface of the inorganic filler is preferably subjected to a silane coupling treatment or a titanium coupling treatment, and a surface treatment agent having a functional group capable of reacting with a binder species on the filler surface is preferably used.
It is preferable that the addition amount of an inorganic filler is 5-30 mass% in the total solid of an anti-glare layer, More preferably, it is 8-20 mass%. In addition, since the inorganic filler has a particle size sufficiently shorter than the wavelength of light, scattering does not occur, and the dispersion in which the filler is dispersed in the binder polymer has the property of an optically uniform substance.

[Configuration of anti-glare film]
In general, the antiglare film of the present invention has a configuration in which an antiglare layer is coated on a transparent support in the simplest configuration.
Although the example of the preferable layer structure of the anti-glare film of this invention is shown below, it is not necessarily limited only to these layer structures.
Support / antiglare layerSupport / hard coat layer / antiglare layerSupport / antiglare layer / hard coat layerSupport / antiglare layer / low refractive index layer / support / hard coat layer / antireflection Dazzle layer / low refractive index layer / support / antiglare layer / hard coat layer / low refractive index layer

[Low refractive index layer]
In the present invention, a low refractive index layer can also be formed on the antiglare layer. The low refractive index layer preferably has a lower refractive index than the antiglare layer. The thickness of the low refractive index layer is preferably 50 to 200 nm, more preferably 70 to 150 nm, and most preferably 80 to 120 nm.

The refractive index of the low refractive index layer is lower than the refractive index of the layer immediately below, preferably 1.20 to 1.55, more preferably 1.25 to 1.46, and 1.30 to 1. .40 is particularly preferred. The thickness of the low refractive index layer is preferably 50 to 200 nm, and more preferably 70 to 100 nm. The low refractive index layer is preferably obtained by curing a curable composition for forming the low refractive index layer.
As a preferred embodiment of the curable composition of the low refractive index layer,
(1) A composition containing a fluorine-containing compound having a crosslinkable or polymerizable functional group,
(2) a composition comprising as a main component a hydrolysis-condensation product of a fluorine-containing organosilane material;
(3) a composition containing a monomer having two or more ethylenically unsaturated groups and inorganic fine particles (in particular, inorganic fine particles having a hollow structure are preferred);
Etc.
Regarding (1) and (2), it is preferable to contain inorganic fine particles, and when inorganic fine particles having a hollow structure with a low refractive index are used, viewpoints such as lowering the refractive index and adjusting the amount of added inorganic fine particles and the refractive index. Is particularly preferable.

(1) Fluorine-containing compound having a crosslinkable or polymerizable functional group As the fluorine-containing compound having a crosslinkable or polymerizable functional group, co-polymerization of a fluorine-containing monomer and a monomer having a crosslinkable or polymerizable functional group Coalescence can be mentioned. Specific examples of these fluoropolymers are described in JP2003-222702A, JP2003-183322A, and the like.

  As described in JP 2000-17028 A, a curing agent having a polymerizable unsaturated group may be used in combination with the above polymer. Moreover, combined use with the compound which has a fluorine-containing polyfunctional polymerizable unsaturated group as described in Unexamined-Japanese-Patent No. 2002-145952 is also preferable. Examples of the compound having a polyfunctional polymerizable unsaturated group include monomers having two or more ethylenically unsaturated groups described as the curable resin compound for the antiglare layer. Moreover, the hydrolysis-condensation product of the organolane described in Unexamined-Japanese-Patent No. 2004-170901 is also preferable, and the hydrolysis-condensation product of the organosilane containing a (meth) acryloyl group is especially preferable. These compounds are particularly preferred because they have a large combined effect for improving scratch resistance, particularly when a compound having a polymerizable unsaturated group is used in the polymer body.

  When the polymer itself does not have sufficient curability, necessary curability can be imparted by blending a crosslinkable compound. For example, when the polymer body contains a hydroxyl group, various amino compounds are preferably used as the curing agent. The amino compound used as the crosslinkable compound is, for example, a compound containing one or both of a hydroxyalkylamino group and an alkoxyalkylamino group in total, specifically, for example, a melamine compound, Examples include urea compounds, benzoguanamine compounds, glycoluril compounds, and the like. For curing these compounds, an organic acid or a salt thereof is preferably used.

(2) Composition mainly composed of hydrolyzed condensate of fluorine-containing organosilane material The composition mainly composed of hydrolyzed condensate of fluorine-containing organosilane compound also has a low refractive index and the hardness of the coating surface. Is preferable. A condensate of a tetraalkoxysilane with a hydrolyzable silanol-containing compound at one or both ends with respect to the fluorinated alkyl group is preferred. Specific compositions are described in JP-A Nos. 2002-265866 and 317152.

(3) A composition containing a monomer having two or more ethylenically unsaturated groups and inorganic fine particles having a hollow structure As yet another preferred embodiment, a low refractive index layer comprising low refractive index particles and a binder can be mentioned. . The low refractive index particles may be organic or inorganic, but particles having pores inside are preferable. Specific examples of the hollow particles are described in the silica-based particles described in JP-A-2002-79616. The particle refractive index is preferably 1.15 to 1.40, more preferably 1.20 to 1.30. Examples of the binder include monomers having two or more ethylenically unsaturated groups described on the page of the antiglare layer.

  It is preferable to add the above-mentioned photo radical polymerization initiator or thermal radical polymerization initiator to the composition for the low refractive index layer used in the present invention. When a radically polymerizable compound is contained, 1 to 10 parts by mass, preferably 1 to 5 parts by mass of a polymerization initiator can be used with respect to the compound.

  In the low refractive index layer used in the present invention, inorganic particles can be used in combination. In order to impart scratch resistance, fine particles having a particle size of 15% to 150%, preferably 30% to 100%, more preferably 45% to 60% of the thickness of the low refractive index layer can be used. .

  In the present invention, the low refractive index layer is provided with a known polysiloxane-based or fluorine-based antifouling agent, slipping agent, etc. for the purpose of imparting antifouling properties, water resistance, chemical resistance, slipping properties and the like. It can be added as appropriate.

  Examples of the additive having a polysiloxane structure include reactive group-containing polysiloxanes {for example, “KF-100T”, “X-22-169AS”, “KF-102”, “X-22-3701IE”, “X-22”. -164B "," X-22-5002 "," X-22-173B "," X-22-174D "," X-22-167B "," X-22-161AS "(product name), "AK-5", "AK-30", "AK-32" (trade name), manufactured by Toa Gosei Co., Ltd .; "Silaplane FM0725", "Silaplane FM0721" It is also preferable to add (trade name), manufactured by Chisso Corporation, etc.}. Moreover, the silicone type compound of Table 2 and Table 3 of Unexamined-Japanese-Patent No. 2003-112383 can also be used preferably.

As the fluorine compound, a compound having a fluoroalkyl group is preferable. The fluoroalkyl group preferably has 1 to 20 carbon atoms, more preferably 1 to 10 carbon atoms, and a straight chain (for example, —CF ₂ CF ₃ , —CH ₂ (CF ₂ ) ₄ H, —CH ₂ (CF ₂ ) ₈ CF ₃ , —CH ₂ CH ₂ (CF ₂ ) ₄ H, etc.), even branched structures (eg, CH (CF ₃ ) ₂ , CH ₂ CF (CF ₃ ) ₂ , CH (CH ₃ ) CF ₂ CF ₃ , CH (CH ₃ ) (CF ₂ ) ₅ CF ₂ H, etc.), alicyclic structures (preferably 5-membered or 6-membered rings such as perfluorocyclohexyl group, perfluorocyclopentyl, etc. Group or an alkyl group substituted with these, and may have an ether bond (for example, CH ₂ OCH ₂ CF ₂ CF ₃ , CH ₂ CH ₂ OCH ₂ C ₄ F ₈ H, CH ₂ CH _{2 CH 2 CH 2 C 8 F 17} , CH 2 CH 2 OCF 2 CF 2 OCF 2 CF 2 H , etc.). A plurality of the fluoroalkyl groups may be contained in the same molecule.

It is preferable that the fluorine-based compound further has a substituent that contributes to bond formation or compatibility with the low refractive index layer film. The substituents may be the same or different, and a plurality of substituents are preferable. Examples of preferred substituents include acryloyl group, methacryloyl group, vinyl group, aryl group, cinnamoyl group, epoxy group, oxetanyl group, hydroxyl group, polyoxyalkylene group, carboxyl group, amino group and the like. The fluorine-based compound may be a polymer or an oligomer with a compound not containing a fluorine atom, and the molecular weight is not particularly limited. Although there is no restriction | limiting in particular in fluorine atom content of a fluorine-type compound, It is preferable that it is 20 mass% or more, It is especially preferable that it is 30-70 mass%, It is most preferable that it is 40-70 mass%. Examples of preferred fluorine-based compounds include Daikin Chemical Industries, Ltd., R-2020, M-2020, R-3833, M-3833, Optool DAC (trade name), Dainippon Ink Co., Ltd. Examples include, but are not limited to, F-171, F-172, F-179A, defender MCF-300, MCF-323 (named above).
These polysiloxane fluorine-based compounds and compounds having a polysiloxane structure are preferably added in the range of 0.1 to 10% by mass, particularly preferably 1 to 5% by mass of the total solid content of the low refractive index layer. It is.

[Transparent support]
There is no limitation in particular as a transparent support body in this invention, such as a transparent resin film, a transparent resin board, a transparent resin sheet. Transparent resin films include cellulose acylate films (for example, cellulose triacetate film (refractive index 1.48), cellulose diacetate film, cellulose acetate butyrate film, cellulose acetate propionate film), polyethylene terephthalate film, polyethersulfone. Films, polyacrylic resin films, polyurethane resin films, polyester films, polycarbonate films, polysulfone films, polyether films, polymethylpentene films, polyetherketone films, (meth) acrylonitrile films, and the like can be used.

Among them, a cellulose acylate film that is highly transparent, optically less birefringent, easy to manufacture, and generally used as a protective film for a polarizing plate is preferable, and a cellulose triacetate film is more preferable.
The thickness of the transparent support is 30 to 65 μm, preferably 35 to 60 μm, and more preferably 40 to 60 μm for thinning.

In the present invention, it is preferable to use cellulose acetate having an acetylation degree of 59.0 to 61.5% for the cellulose acylate film.
The degree of acetylation means the amount of bound acetic acid per unit mass of cellulose. The degree of acetylation follows the measurement and calculation of the degree of acetylation in ASTM: D-817-91 (test method for cellulose acetate and the like). The viscosity average degree of polymerization (DP) of cellulose acylate is preferably 250 or more, and more preferably 290 or more.
The cellulose acylate used in the present invention has a Mw / Mn (Mw is a mass average molecular weight, Mn is a number average molecular weight) value by gel permeation chromatography close to 1.0, in other words, a molecular weight distribution. Narrow is preferred. The specific value of Mw / Mn is preferably 1.0 to 1.7, more preferably 1.3 to 1.65, and most preferably 1.4 to 1.6. preferable.

In general, the 2, 3, and 6 hydroxyl groups of cellulose acylate are not evenly distributed by 1/3 of the total substitution degree, and the substitution degree of the 6-position hydroxyl group tends to be small. In the present invention, it is preferable that the substitution degree of the 6-position hydroxyl group of cellulose acylate is larger than that of the 2- and 3-positions. The hydroxyl group at the 6-position with respect to the total substitution degree is preferably substituted with 32% or more of an acyl group, more preferably 33% or more, and particularly preferably 34% or more. Furthermore, the substitution degree of the 6-position acyl group of cellulose acylate is preferably 0.88 or more. The 6-position hydroxyl group may be substituted with a propionyl group, butyroyl group, valeroyl group, benzoyl group, acryloyl group or the like, which is an acyl group having 3 or more carbon atoms, in addition to the acetyl group. The degree of substitution at each position can be determined by NMR.
In the present invention, as cellulose acylate, paragraphs “0043” to “0044” [Example] [Synthesis Example 1], paragraphs “0048” to “0049” [Synthesis Example 2], and paragraph “ Cellulose acetate obtained by the method described in “0051” to “0052” [Synthesis Example 3] can be used.

  The transparent support preferably contains the sugar ester compound described below. By containing the sugar ester compound, the crying out of the plasticizer from the transparent support to the antiglare layer is reduced, and high hardness can be obtained.

(Sugar ester compound)
-Sugar residue-
The sugar ester compound refers to a compound in which at least one substitutable group (for example, a hydroxyl group or a carboxyl group) in the polysaccharide constituting the compound and at least one substituent are ester-bonded. . That is, the sugar ester compound referred to here includes a wide range of sugar derivatives, for example, a compound containing a sugar residue such as gluconic acid as a structure. That is, the sugar ester compound includes an ester of glucose and carboxylic acid and an ester of gluconic acid and alcohol.
The substitutable group in the polysaccharide constituting the sugar ester compound is preferably a hydroxyl group.

  The sugar ester compound includes a structure derived from a polysaccharide constituting the sugar ester compound (hereinafter also referred to as a sugar residue). The structure of the sugar residue per monosaccharide is referred to as the structural unit of the sugar ester compound. The structural unit of the sugar ester compound preferably includes a pyranose structural unit or a furanose structural unit, and more preferably all sugar residues are a pyranose structural unit or a furanose structural unit. Further, when the sugar ester is composed of a polysaccharide, it preferably contains both a pyranose structural unit or a furanose structural unit.

  The sugar residue of the sugar ester compound may be derived from 5 monosaccharides or 6 monosaccharides, but is preferably derived from 6 monosaccharides.

The number of structural units contained in the sugar ester compound is preferably 1 to 4. That is, the sugar ester compound is preferably an esterified compound of a compound having at least one furanose structure or at least one pyranose structure.
The number of structural units contained in the sugar ester compound is preferably 2 to 4, more preferably 2 to 3, and particularly preferably 2. That is, the sugar constituting the sugar ester compound is preferably a disaccharide to a tetrasaccharide, more preferably a disaccharide to a trisaccharide, and particularly preferably a disaccharide.

  The sugar ester compound is more preferably a sugar ester compound containing 2 to 4 pyranose structural units or furanose structural units in which at least one hydroxyl group is esterified, and a pyranose structure in which at least one hydroxyl group is esterified A sugar ester compound containing two units or two furanose structural units is more preferable.

  Examples of the monosaccharides or saccharides containing 2 to 4 monosaccharide units include, for example, erythrose, threose, ribose, arabinose, xylose, lyxose, allose, altrose, glucose, fructose, mannose, gulose, idose, galactose , Talose, trehalose, isotrehalose, neotrehalose, trehalosamine, caudibiose, nigerose, maltose, maltitol, isomaltose, sophorose, laminaribiose, cellobiose, gentiobiose, lactose, lactosamine, lactitol, lactulose, melibiose, primebelloose, rutiose , Sucrose, sucralose, turanose, vicyanose, cellotriose, cacotriose, gentianose, isomaltori , Isopanose, maltotriose, manninotriose, melenitoose, panose, planteose, raffinose, solatriose, umbelliferose, lycotetraose, maltotetraose, stachyose, baltopentaose, velval course, maltohexaose , Xylitol, sorbitol and the like.

  Preferably, ribose, arabinose, xylose, lyxose, glucose, fructose, mannose, galactose, trehalose, maltose, cellobiose, lactose, sucrose, sucralose, xylitol, sorbitol, more preferably arabinose, xylose, glucose, fructose, mannose , Galactose, maltose, cellobiose and sucrose, particularly preferably xylose, glucose, fructose, mannose, galactose, maltose, cellobiose, sucrose, xylitol and sorbitol.

  Preferred examples of the substituent of the sugar ester compound include an alkyl group (preferably an alkyl group having 1 to 22 carbon atoms, more preferably 1 to 12 carbon atoms, and particularly preferably an alkyl group having 1 to 8 carbon atoms, such as a methyl group, An ethyl group, a propyl group, a hydroxyethyl group, a hydroxypropyl group, a 2-cyanoethyl group, a benzyl group, etc.), an aryl group (preferably having a carbon number of 6 to 24, more preferably 6 to 18 and particularly preferably 6 to 12). A group such as a phenyl group or a naphthyl group, an acyl group (preferably having a carbon number of 1 to 22, more preferably a carbon number of 2 to 12, particularly preferably a carbon number of 2 to 8, such as an acetyl group or a propionyl group, Butyryl group, pentanoyl group, hexanoyl group, octanoyl group, benzoyl group, toluyl group, phthalyl group), amide group (preferred) Or an amide group (preferably 4 to 22 carbon atoms, more preferably an amide having 2 to 12 carbon atoms, particularly preferably an amide having 2 to 8 carbon atoms, such as a formamide group or an acetamide group). May include amide groups having 4 to 12 carbon atoms, particularly preferably 4 to 8 carbon atoms (for example, succinimide group, phthalimide group, etc.). Among them, an alkyl group or an acyl group is more preferable, a methyl group, an acetyl group, or a benzoyl group is more preferable, and at least one of a benzoyl group and an acetyl group is particularly preferable, and a benzoyl group is more particularly preferable.

Among the sugar esters, it is preferable to contain an aromatic sugar ester compound represented by the following general formula (1) and an aliphatic sugar ester compound represented by the following general formula (2).
General formula (1) (HO) m-G- (LR- ¹ ) n
Formula (2) (HO) t- G '- (L'-R 2) r
(In the general formulas (1) and (2), G and G ′ each independently represent a monosaccharide residue or a disaccharide residue. R ¹ each independently represents an aliphatic group or an aromatic group, and at least 1 Each represents an aromatic group, R ² independently represents an aliphatic group, L and L ′ each independently represent a divalent linking group, and m, n, r and t each represents an integer of 0 or more. However, m + n and r + t are respectively equal to the number of hydroxyl groups when it is assumed that G is not a residue but an unsubstituted saccharide having a cyclic acetal structure of the same skeleton.)

The sugar ester compound represented by the general formula (1) or (2) that can be used in the present invention is preferably a compound having a furanose structure or a pyranose structure.
As the upper limit values of m + n and r + t, values determined by the type of G or G ′ can be adopted. If G or G ′ is a monosaccharide residue, it is 5; It becomes.

  The sugar ester compound represented by the general formula (1) or (2) is a compound (A) in which the G or G ′ having one furanose structure or one pyranose structure is a monosaccharide residue, or It is an esterified compound obtained by esterifying all or part of the OH group in the compound (B) in which G or G ′ is a disaccharide residue in which at least one of a furanose structure or a pyranose structure is linked. Is preferred.

Examples of compound (A) include, but are not limited to, glucose, galactose, mannose, fructose, xylose, or arabinose.
Examples of the compound (B) include lactose, sucrose, nystose, 1F-fructosyl nystose, stachyose, maltitol, lactitol, lactulose, cellobiose, maltose, cellotriose, maltotriose, raffinose or kestose. Other examples include gentiobiose, gentiotriose, gentiotetraose, xylotriose, galactosyl sucrose, and the like, but are not limited thereto.
Of these compounds (A) and (B), compounds having both a furanose structure and a pyranose structure are particularly preferable. As an example, sucrose, kestose, nystose, 1F-fukratosyl nystose, stachyose and the like are preferable, and sucrose is more preferable. In addition, in the compound (B), a compound in which at least one of a furanose structure or a pyranose structure is bonded is also one of preferred embodiments.

There is no restriction | limiting in particular as a substituent used in esterifying all or one part of OH group in a compound (A) and a compound (B). Among these, it is preferable to use monocarboxylic acid. That is, it is preferable that R ¹ in the general formula (1) and R ² in the general formula (2) each independently represent an acyl group.
There is no restriction | limiting in particular as said monocarboxylic acid, Well-known aliphatic monocarboxylic acid, alicyclic monocarboxylic acid, aromatic monocarboxylic acid, etc. can be used. The carboxylic acid used may be one kind or a mixture of two or more kinds. When there are a plurality of R ¹ or R ² , they may be the same or different.

On the other hand, L in the general formula (1) and L ′ in the general formula (2) are each independently a single bond, —O—, —CO—, —NR ¹¹ — (R ¹¹ is 1 It is preferable to represent any one of a valent substituent, and when there are a plurality of L ¹ or L ′, they may be the same as or different from each other. Among them, it is preferable that L ¹ or L ′ represents —O— from the viewpoint that R ¹ and R ² can be easily substituted with an acyl group.

  In the present invention, as a transparent support, a polyethylene terephthalate film is also excellent in transparency, mechanical strength, flatness, chemical resistance and moisture resistance, and is inexpensive and preferably used. In order to further improve the adhesion strength between the transparent support and the antiglare layer provided thereon, the polyethylene terephthalate film is more preferably subjected to an easy adhesion treatment. Examples of commercially available PET films with an easily adhesive layer for optics include Cosmo Shine A4100 and A4300 manufactured by Toyobo Co., Ltd.

[Production method of anti-glare film]
In the method for producing an antiglare film of the present invention, the curable composition is applied on a transparent support to form a coating film (coating film), and then the coating film is irradiated with ionizing radiation (preferably ultraviolet rays) and cured. To form an antiglare layer.
Here, solid content ratio of a curable composition is 20-40 mass%, and it is preferable that it is 25-30 mass%. Moreover, the coating amount of the curable composition on the transparent support is 15 to 25 cc / m ² , and more preferably 17 to 20 cc / m ² . By setting the solid content ratio and the coating amount within these ranges, the coating property is excellent and a good surface shape can be obtained.

[Application method]
Each layer of the antiglare film of the present invention can be formed by the following coating method, but is not limited to this method. Dip coating method, air knife coating method, curtain coating method, roller coating method, wire bar coating method, gravure coating method, slide coating method and extrusion coating method (die coating method) (see JP 2003-164788 A), micro Known methods such as a gravure coating method are used, and among them, a micro gravure coating method and a die coating method are preferable.

[Drying and curing conditions]
Preferred examples of drying and curing methods in the case of forming a layer by coating such as an antiglare layer in the present invention are described below.
In the present invention, it is effective to cure by combining irradiation with ionizing radiation and heat treatment before, at the same time as, or after irradiation.
Although the pattern of some manufacturing processes is shown below, it is not limited to these. (In the table below, “-” indicates that no heat treatment was performed.)

  In addition, a step of performing a heat treatment simultaneously with ionizing radiation curing is also preferable.

  In the present invention, as described above, heat treatment is preferably performed in combination with irradiation with ionizing radiation. The heat treatment is not particularly limited as long as the transparent support of the antiglare film and the constituent layers including the antiglare layer are not damaged, but preferably 40 to 150 ° C, more preferably 50 to 130 ° C, and most preferably 60. ~ 110 ° C. Thereby, it is preferable to make solid content concentration in a coating film into 70 mass% or more within 20 seconds after application | coating, and it is still more preferable to set it as 80 mass% or more.

  The time required for the heat treatment varies depending on the molecular weight of the components used, the interaction with other components, the viscosity, etc., but is 15 seconds to 1 hour, preferably 20 seconds to 30 minutes, and most preferably 30 seconds to 5 minutes.

There is no restriction | limiting in particular about the kind of ionizing radiation, Although an X-ray, an electron beam, an ultraviolet-ray, visible light, infrared rays etc. are mentioned, an ultraviolet-ray is preferable. The ultraviolet lamp or the like, preferably ^{100mJ / cm 2 ~1000mJ / cm 2} , more preferably to cure each layer by irradiating ultraviolet rays of energy dose of 150~500mJ / cm ^2.
In the formation of the antiglare layer of the present invention, at the time of irradiation, the amount of energy irradiation may be applied at once, or irradiation may be performed in a divided manner. From the viewpoint of improving curing unevenness, it is preferable to irradiate at least three times. The number of divisions is preferably 3 to 10 times, and more preferably 3 to 5 times.
In the first and second irradiation, the maximum illumination intensity of preferably 5~50mW / cm ^2, more preferably 5~20mW / cm ^2. Irradiation dose is preferably ^{10~100mJ / cm 2, 20~50mJ / cm} 2 is more preferable.
In the third and subsequent irradiations, the maximum illuminance is preferably 20 to 1000 mW / cm ^2, more preferably 50 to 500 mW / cm ² . The irradiation amount may be a total of 100 mJ / cm ² or more, and preferably 100 to 1000 mJ / cm ² , more preferably 150 to 500 mJ / cm ² . is there.
The maximum illuminance of the first and second irradiations is preferably smaller than the maximum illuminance of the third and subsequent irradiations.
By setting the maximum illuminance during the first and second irradiations at the initial stage of curing to a low illuminance of 5 to 50 mW / cm ² , the curing shrinkage stress is alleviated and curing unevenness can be reduced. Moreover, the polymerization rate of the whole layer can be raised by irradiation after the 3rd time, and sufficient hardness can be ensured.
Moreover, you may provide the time which does not irradiate an ultraviolet-ray between several irradiation (For example, between the 1st irradiation and the 2nd irradiation, and between the 2nd irradiation and the 3rd irradiation). Here, non-irradiation means that light is not substantially irradiated, for example, that it is placed in an environment with an illuminance of 1 mW / cm ² or less, preferably 0.2 mW / cm ² or less. By providing such an unirradiated time, the curing shrinkage stress can be relaxed and the curing unevenness can be further reduced.

The divided irradiation may be performed by changing the illuminance and the irradiation amount by the same irradiation source (ultraviolet irradiation device) or by a plurality of irradiation sources corresponding to the number of divisions.
Preferably, it is preferable to install three or more ultraviolet irradiation devices at different locations in the film transport direction, and adjust the illuminance and irradiation amount with each irradiation device.
FIG. 1 schematically shows an example of split irradiation using four ultraviolet irradiation devices. As shown in FIG. 1, ultraviolet irradiation devices 11 to 14 are installed at different locations in the conveyance direction of the film 10, and the film 10 is irradiated by the respective ultraviolet irradiation devices.
In this case, first lamp th and the maximum illumination intensity of the second lamp eye is preferably 5~50mW / cm ^2, more preferably 5~20mW / cm ^2. The maximum illumination intensity of the third lamp and subsequent 20 to 1000 mW / cm ² is more preferably preferably 50 to 500 mW / cm ^2. The number of installed lamps of the ultraviolet irradiation device is preferably 3 to 10 lamps, and more preferably 3 to 5 lamps. The distance between the ultraviolet irradiation apparatuses is not particularly limited, but it is preferable that an area not irradiated with ultraviolet rays is formed between the apparatuses. For example, the non-irradiation time is preferably 2 seconds to 60 seconds, more preferably 10 It is preferable to maintain a distance of ˜20 seconds.
Curing is promoted by setting the maximum illuminance of the first lamp and the second lamp to 5 mW / cm ² or more, and curing unevenness can be reduced by setting the maximum illuminance to 50 mW / cm ² or less. In this way, it is presumed that by irradiating the initial stage of curing with low illuminance, the curing shrinkage stress is relieved and curing unevenness is reduced. It is preferable to increase the polymerization rate of the entire film by setting the maximum illuminance after the third lamp to ²⁰ to 1000 mW / cm ² .

In the ultraviolet irradiation process, the transparent support is wound around a backup roll having a diameter of 400 mm or less (rolls 15 and 16 in FIG. 1), and the tension applied in the transport direction of the transparent support is set to 400 N / m or more, and It is more preferable to perform the above-mentioned divided irradiation in a state where the film surface temperature of the coating film is 25 ° C. or less.
By setting the tension applied in the transport direction to 400 N / m or more and the diameter of the backup roll to 400 mm or less, the holding power against curing shrinkage of the coating film is increased, and uneven curing can be suppressed. Conventionally, since there has been a problem such as occurrence of a nick due to curing, it is common to use a backup roll having a diameter larger than 400 mm. However, in the present invention, the antiglare layer is cured by split irradiation. Accordingly, it is possible to use a backup roll having a diameter of 400 mm or less, and it is possible to further reduce curing unevenness.
The tension applied in the transport direction is preferably 500 N / m or more, more preferably 600 N / m or more. The upper limit is preferably 700 N / m or less. The diameter of the backup roll is preferably 350 mm or less, more preferably 300 mm or less, and preferably 200 mm or more, more preferably 250 mm or more for transporting the film without causing a failure such as a knick. preferable.
By setting the film surface temperature of the coating film to 25 ° C. or less, the elastic modulus of the transparent support can be improved, and uneven curing can be reduced. The film surface temperature is preferably 20 ° C. or less, and more preferably 18 ° C. or less. From the viewpoint of preventing dew condensation, the temperature is preferably 10 ° C or higher, and more preferably 15 ° C or higher.

[Polarizer]
The antiglare film of the present invention can be used for one or both of the protective films of a polarizing plate comprising a polarizing film and protective films disposed on both sides thereof, and can be a polarizing plate having antiglare properties. .

  The antiglare film of the present invention is used as one protective film, and a normal cellulose acetate film may be used as the other protective film, but the other protective film is manufactured by a solution casting method, and It is preferable to use a cellulose acetate film stretched in the width direction in the form of a roll film at a stretch ratio of 10 to 100%.

  Moreover, it is also a preferable aspect that among the two protective films of the polarizing film, the film other than the antiglare film of the present invention is an optical compensation film having an optical compensation layer comprising an optically anisotropic layer. The optical compensation film (retardation film) can improve the viewing angle characteristics of the liquid crystal display screen. A known film can be used as the optical compensation film, but the optical compensation film described in JP-A-2001-100042 is preferable in terms of widening the viewing angle.

  Examples of the polarizing film include an iodine polarizing film, a dye polarizing film using a dichroic dye, and a polyene polarizing film. The iodine polarizing film and the dye polarizing film are generally produced using a polyvinyl alcohol film.

As the polarizing film, a known polarizing film or a polarizing film cut out from a long polarizing film whose absorption axis is neither parallel nor perpendicular to the longitudinal direction may be used. A long polarizing film whose absorption axis is neither parallel nor perpendicular to the longitudinal direction is produced by the following method.
That is, it stretches by applying tension while holding both ends of a polymer film such as a polyvinyl alcohol film continuously supplied by a holding means, and stretches at least 1.1 to 20.0 times in the film width direction. The difference between the longitudinal travel speeds of the holding devices at both ends of the film is within 3%, and the angle formed by the traveling direction of the film at the exit of the step of retaining both ends of the film and the substantial stretching direction of the film is inclined at 20 to 70 °. Thus, it can manufacture by the extending | stretching method formed by bending the film advancing direction in the state which hold | maintained both ends of the film. In particular, those inclined by 45 ° are preferably used from the viewpoint of productivity.

  The method for stretching the polymer film is described in detail in paragraphs 0020 to 0030 of JP-A-2002-86554.

[Image display device]
The antiglare film or polarizing plate of the present invention can be used for an image display device such as a liquid crystal display device (LCD), a plasma display panel (PDP), an electroluminescence display (ELD), or a cathode ray tube display device (CRT). .

  In order to describe the present invention in detail, examples will be described below, but the present invention is not limited to these examples.

[Examples 101 to 117 and Comparative examples 101 to 112]
(Preparation of particle dispersion)
The dispersions D101 to D106 of translucent resin particles having the compositions shown in Table 2 below are obtained by adding translucent resin particles in a stirred MIBK (methyl isobutyl ketone) solution to a solid content concentration of 30% by mass. It added gradually until it became, and it stirred for 30 minutes and produced. Dispersion D107 was gradually added to the stirring MIBK (methyl isobutyl ketone) solution until the translucent resin particles and Disperbyk-166 reached a solid content concentration of 45 mass%, and stirred for 30 minutes. Made. The numerical values in Table 2 represent “parts by mass” of each component.

The translucent resin particles described in Table 2 are the following particles.
A: Cross-linked methyl methacrylate-styrene copolymer particles having an average particle diameter of 1.5 μm (refractive index of 1.525)
B: Cross-linked methyl methacrylate-styrene copolymer particles having an average particle size of 2.0 μm (refractive index: 1.525)
C: Cross-linked methyl methacrylate-styrene copolymer particles having an average particle size of 2.5 μm (refractive index: 1.525)
D: average particle diameter 3.0 μm crosslinked methyl methacrylate-styrene copolymer particles (refractive index 1.525)
E: average particle diameter 6.0 μm crosslinked methyl methacrylate-styrene copolymer particles (refractive index 1.525)
F: average particle diameter 0.7 μm crosslinked methyl methacrylate-styrene copolymer particles (refractive index 1.525)
Disperbyk-166 (trade name) (amine value 20 KOH / g) is a polymer compound manufactured by Big Chemie.

(Preparation of coating solution for antiglare layer)
Each component was added with the composition shown in Table 3 below, and filtered through a polypropylene filter having a pore diameter of 30 μm to prepare antiglare layer coating solutions A101 to A113 and B101 to B110. The numerical values in Table 3 represent “parts by mass” of each component.

The compounds used are shown below.
A-DPH: Dipentaerythritol hexaacrylate (manufactured by Shin-Nakamura Chemical Co., Ltd.) acrylic equivalent 96
PET-30: A mixture of pentaerythritol triacrylate and pentaerythritol tetraacrylate [manufactured by Nippon Kayaku Co., Ltd.] acrylic equivalent 88
Biscote 360: trimethylolpropane EO addition triacrylate [manufactured by Osaka Organic Chemical Industry Co., Ltd.] acrylic equivalent 150
UV1700B: urethane acrylate (manufactured by Nippon Synthetic Chemical Industry Co., Ltd., acrylic equivalent 112)
CAB: cellulose acetate butyrate 531-1 [manufactured by Eastman Kodak]
Irgacure 819: Bis (2,4,6-trimethylbenzoyl) -phenylphosphine oxide [phosphine oxide photopolymerization initiator, manufactured by BASF]
Irgacure 369: 2-Benzyl-2-dimethylamino-1- (4-morpholinophenyl) -butanone-1 [α-aminoalkylphenone photopolymerization initiator, manufactured by BASF]
Irgacure 907: 2-methyl-1- (4-methylthiophenyl) -2-morpholinopropan-1-one [α-aminoalkylphenone photopolymerization initiator, manufactured by BASF]
Irgacure 184: 1-Hydroxy-cyclohexyl-phenyl-ketone [Alkylphenone photopolymerization initiator, manufactured by BASF]
SP-13: The following fluorosurfactant

(Coating of antiglare layer)
A triacetyl cellulose film having a thickness of 60 μm, 40 μm, or 35 μm was unwound in a roll form, and antiglare film samples were prepared using coating solutions A101 to A113 and B101 to B110 for the antiglare layer. Specifically, in the die coating method using the slot die described in JP-A-2006-122889, Example 1, each coating solution was applied under the condition of a conveyance speed of 30 m / min, and after drying at 60 ° C. for 150 seconds, Furthermore, using an air-cooled metal halide lamp (manufactured by Eye Graphics Co., Ltd.) with an oxygen concentration of about 0.1% under a nitrogen purge, ultraviolet rays having an illuminance of 150 mW / cm ² and an irradiation amount of 150 mJ / cm ² were irradiated. After the coating film was cured to form an antiglare layer, it was wound up. Under the present circumstances, the film surface temperature of the coating film was 18 degreeC, the conveyance direction tension | tensile_strength of the support body was 350 N / m, and the anti-glare film was created using the backup roll of diameter 500mm.

(Saponification treatment of antiglare film)
The obtained antiglare film was saponified and dried under the following conditions.
Alkaline bath: 1.5 mol / dm 3 aqueous sodium hydroxide solution at 55 ° C. for 120 seconds.
First washing bath: tap water, 60 seconds.
Neutralization bath: 0.05 mol / dm 3 sulfuric acid, 30 ° C.-20 seconds.
Second washing bath: tap water, 60 seconds.
Drying: 120 ° C., 60 seconds.

(Preparation of polarizing plate for front)
A triacetyl cellulose film that has been neutralized and washed with a 1.5 mol / L, 55 ° C. NaOH aqueous solution for 2 minutes, and each saponified film in an antiglare film are allowed to adsorb iodine to polyvinyl alcohol. A polarizing plate for front was prepared by adhering and protecting both sides of a polarizer produced by stretching. At this time, the film thickness of the triacetyl cellulose film was the same as the corresponding antiglare film.

(Preparation of rear polarizing plate)
A rear polarizing plate was produced in the same manner as the front polarizing plate except that the antiglare film was changed to the optical compensation film shown below.

(Production of optical compensation film)
The inner layer and outer layer dopes having the following compositions were respectively prepared.
Composition of inner layer dope:
Cellulose acetate C-1 100 parts by mass (acetyl substitution degree 2.81, number average molecular weight 88000)
7 parts by mass of the following retardation developer

The following polymer P-2 9.0 parts by mass The following dye (Bluing dye) 0.000078 parts by mass

Dichloromethane 423.9 parts by mass Methanol 63.3 parts by mass

Composition of outer layer dope:
Cellulose acetate C-1 100 parts by mass (acetyl substitution degree 2.81, number average molecular weight 88000)
7 parts by mass of the retardation developing agent 9.0 parts by mass of the following polymer P-2 0.000078 parts by mass Silica particles having an average particle diameter of 16 nm 0.14 parts by mass
("AEROSIL R972" manufactured by Nippon Aerosil Co., Ltd.)
Dichloromethane 424.5 parts by mass Methanol 63.4 parts by mass

Polymer P-2: polycondensation comprising a dicarboxylic acid residue of TPA / PA / SA / AA (= 45/5/30/20 (mol%)) and a diol residue of ethylene glycol (100 mol%) A polycondensate having both ends sealed with acetyl ester residues and having a number average molecular weight of 900 (where TPA is terephthalic acid, PA is phthalic acid, SA is sebacic acid, AA is adipine) Acid.)

  The outer layer and inner layer dope solutions having the above composition are uniformly and simultaneously laminated on a stainless steel band support with a width of 2000 mm so as to form a three-layer structure of an outer layer on the support surface side, an inner layer, and an outer layer on the air interface side using a band casting apparatus. Casted. With the stainless steel band support, the solvent was evaporated until the residual solvent amount was 40% by mass, and the stainless steel band support was peeled off. Stretching is applied to stretch so that the longitudinal (MD) stretch ratio is 1.02, then both ends are held by a tenter, and the stretch ratio in the width (TD) direction is 1.22 times. Thus, the film was stretched in the transverse direction (lateral stretching) at a rate of 45% / min. The residual solvent amount at the start of stretching was 30% by mass. It was made to dry for 35 minutes in a 115 degreeC drying zone, conveying after extending | stretching. After drying, it is slit to 1340 mm width, and the optical film thickness ratio of each layer is a support surface side outer layer: inner layer: air interface side outer layer = 3: 94: 3, and consists of a cellulose acylate film with a total film thickness of 60 μm, 40 μm, 35 μm Each film was obtained.

(Production of liquid crystal display device)
The front and rear polarizing plates and retardation film provided in the VA type liquid crystal display device (LC-32DZ3 Sharp Corporation) are peeled off, and the respective polarizing plates prepared above are used instead. Cellulose film is arranged so that the optical compensation film is on the liquid crystal cell side at the rear, and the transmission axis is pasted so as to match the polarizing plate pasted on the product, thereby producing a liquid crystal display device having an antiglare film. did. The rear polarizing plate used was an optical compensation film having the same thickness as the triacetyl cellulose film used for the front antiglare film.

(Evaluation of anti-glare film and liquid crystal display device)
The following evaluation was performed with respect to the obtained anti-glare film and the liquid crystal display device.
<1> Pencil hardness The obtained antiglare film was evaluated by a pencil hardness test according to JIS-K5400.
In the present invention, 2H or more was regarded as acceptable (◯), and the failure was regarded as x. Table 3 shows the pencil hardness that passed, and the number in parentheses () that was not damaged when it was cut five times with 2H.

<2> Antiglare property The produced antiglare film was mounted on a liquid crystal television (LC-32DZ3 Sharp Corporation), and the degree of reflection of an object in black display was visually evaluated according to the following criteria.
I don't mind the reflection at all: ◎
I don't really care about the reflections: ○ ～ ◎
A little worried about the reflection: ○
I am very worried about the reflection: ×

<3> Planar (curing unevenness)
The produced anti-glare film was mounted on a liquid crystal television (LC-32DZ3 Sharp Corporation), and the surface condition in black display was visually evaluated in the bright room environment according to the following criteria. Here, the curing unevenness is unevenness that occurs substantially in parallel with the conveying direction when the antiglare film is produced and is observed in a streak shape.
I do not care about unevenness at all: ◎
Unevenness is almost not noticed: ○ ～ ◎
I'm worried about some unevenness: ○
Unevenness is very worrisome: ×

<4> Rough feeling The produced anti-glare film was mounted on a liquid crystal television (LC-32DZ3 Sharp Corporation), and the rough feeling on the black surface of the liquid crystal television was visually evaluated under the following criteria in a bright room environment. . A display image with black tightening is obtained as the roughness becomes better.
I do not mind the feeling of roughness at all: ◎
I do not mind the rough feeling ： ○ ～ ◎
I'm a little worried about the roughness: ○
I'm very worried about the rough feeling: ×

<5> Haze The total haze value (H) of the obtained light diffusion film was measured according to JIS-K7136. Nippon Denshoku Industries Co., Ltd. haze meter NDH2000 was used for the apparatus.

<6> Curl The curl was measured according to the stencil method for curl measurement of Method A in “Measuring Method of Curling of Photographic Film” of JIS-K7619-1988.
The measurement conditions are 25 ° C., relative humidity 60%, humidity control time 5 hours, and are the values when curl is expressed by the following mathematical formula.
(Formula curl = 1 / R R is the radius of curvature (m)

  Table 4 below shows the evaluation results of the antiglare film, the polarizing plate using the antiglare film, and the image display device.

  As shown in Table 4, the antiglare film of the present invention is suppressed in uneven curing, and is excellent in hardness, roughness, and antiglare properties.

[Examples 201 to 206]
(Coating of antiglare layer)
In producing the antiglare films of Examples 201 to 206, the film surface temperature at the time of ultraviolet curing, the conveying direction tension, the backup roll diameter, the UV irradiation pattern (the illuminance of UV1 to UV5) from the production methods of Examples 101 to 115. Were changed as shown in Table 4 below to produce an antiglare film.
No irradiation (illuminance of 0.2 mW / cm ² or less) was not provided between UV1 and UV2, and a non-irradiation time of 3 seconds was provided between UV2 and UV3. It was also a dose 300 J / cm ² in total UV1～UV5.
Using the produced anti-glare film, a polarizing plate was produced and attached to an image display device in the same manner as in Examples 101 to 115, and evaluated. The evaluation results are shown in Table 5.

  As shown in Table 5, it was found that curling value can be reduced and curing unevenness can be improved by increasing the conveyance tension, decreasing the backup roll diameter, and performing the divided irradiation.

[Examples 301 to 302]
A cellulose ester film containing an esterified compound of a compound having 1 or more and 4 or less of at least one of a furanose structure or a pyranose structure was produced by the following method. Antiglare films 301 to 302 were produced in the same manner as in Example 206 except that the transparent support was changed to the obtained cellulose ester film. Using the produced anti-glare film, a polarizing plate was produced and attached to an image display device in the same manner as in Examples 101 to 115, and evaluated. The evaluation results are shown in Table 6.

<Method for producing cellulose ester film>
(Preparation of cellulose acylate)
Cellulose acylate was synthesized by the method described in JP-A-10-45804 and 08-231761, and the degree of substitution was measured. Specifically, sulfuric acid (7.8 parts by mass with respect to 100 parts by mass of cellulose) was added as a catalyst, carboxylic acid serving as a raw material for the acyl substituent was added, and an acylation reaction was performed at 40 ° C. At this time, the kind and substitution degree of the acyl group were adjusted by adjusting the kind and amount of the carboxylic acid. In addition, aging was performed at 40 ° C. after acylation. Further, the low molecular weight component of the cellulose acylate was removed by washing with acetone.

(Preparation of dope for core layer)
The following composition was put into a mixing tank and stirred to dissolve each component, and a cellulose acylate solution was prepared as a core layer dope. The amount of the solvent (methylene chloride / methanol / butanol = 84/15/1) was appropriately adjusted so that the solid content concentration of each cellulose acylate solution was 23.5% by mass.
Cellulose acylate (acetyl substitution degree 2.85) 100.0 parts by mass Sugar ester (compound 1 below) 11.0 parts by mass UV absorber (UV-1 below) 2.0 parts by mass Solvent 365.5 Parts by mass

(Compound 1)

(Preparation of surface layer dope)
The following composition was put into a mixing tank and stirred to dissolve each component, and a cellulose acylate solution was prepared as a dope for the surface layer. The amount of the solvent (methylene chloride / methanol / butanol = 84/15/1) was appropriately adjusted so that the solid content concentration of each cellulose acylate solution was 18.0% by mass.
Cellulose acylate (acetyl substitution degree 2.81) 100.0 parts by mass UV absorber (UV-1 below) 1.0 part UV absorber (UV-2 below) 1.0 part UV absorber Agent (UV-3 below) 1.0 part by mass

(Production of cellulose ester film)
A surface layer having a film thickness of 5 μm on the core layer dope so that the core layer dope becomes a core layer having a film thickness of 55 μm so as to be in contact with a metal band support cooled to −10 ° C. The core layer dope was co-cast from the die so that the core layer dope was in contact with the support. The obtained web (film) was peeled off from the band, dried while being conveyed at 30 to 40 ° C., then framed and post-dried at 130 ° C. for 20 minutes. In Example 302, a film was prepared in the same manner except that the thickness of the core layer was changed to 35 μm.

<Preparation of antireflection film>
[Coating of low refractive index layer]
(Preparation of inorganic particle dispersion (B-1))
By changing the preparation conditions from Preparation Example 4 of JP-A-2002-79616, silica fine particles having cavities therein were produced. The solvent was replaced with methanol from the aqueous dispersion state. Finally, the solid content concentration was adjusted to 20% by mass to obtain particles having an average particle diameter of 45 nm, a shell thickness of about 7 nm, and a silica particle refractive index of 1.30. This is designated as dispersion (B).
After adding 15 parts by mass of acryloyloxypropyltrimethoxysilane and 1.5 parts by mass of diisopropoxyaluminum ethyl acetate to 500 parts by mass of the dispersion (B), 9 parts by mass of ion-exchanged water was added. . After making it react at 60 degreeC for 8 hours, it cooled to room temperature and added 1.8 mass parts of acetylacetone. Further, MEK was added so that the total liquid amount was almost constant, the solvent was replaced by distillation under reduced pressure, and finally the dispersion (B-1) was prepared by adjusting the solid content concentration to 20% by mass. did.

(Preparation of coating solution for low refractive index layer)
7.6 g of fluorine-containing polymer (P-12: fluorine-containing copolymer, exemplified compound of JP 2007-293325 A), 1.4 g of DPHA, 2.4 g of dispersion (B-1), photopolymerization An initiator (Irgacure 907) 0.46 g, methyl ethyl ketone 190 g, and propylene glycol monomethyl ether acetate 48 g were added, and after stirring, the mixture was filtered through a polypropylene filter having a pore size of 5 μm to prepare a coating solution for a low refractive index layer.

(Coating of low refractive index layer)
The anti-glare films of Examples 101 to 115, 201 to 206, and 301 to 302 were unwound again, and the coating solution for the low refractive index layer was subjected to the condition of a conveyance speed of 30 m / min by the die coating method using the slot die. The coating was dried at 90 ° C. for 75 seconds, and an air-cooled metal halide lamp (made by Eye Graphics Co., Ltd.) with an oxygen concentration of 0.01 to 0.1% under a nitrogen purge was used, and an illuminance of 400 mW / An antiglare film having a low refractive index layer was produced by irradiating ultraviolet rays with a cm ² and an irradiation amount of 240 mJ / cm ² to form a low refractive index layer having a thickness of 100 nm and winding. The refractive index of the low refractive index layer was 1.36. The antiglare film provided with the low refractive index layer was further improved in black tightening properties, and a high quality antiglare film with an antireflection function could be obtained.

10 Film 11-14 Ultraviolet irradiation device 15, 16 roll

Claims (9)

An antiglare film having an antiglare layer having a thickness of 2.0 to 5.0 μm on a transparent support having a thickness of 30 to 65 μm,
The antiglare layer has a crosslinked acrylic resin in which an acrylic compound having an average acrylic equivalent of 100 or less is cross-linked, and translucent particles having an average particle diameter of 1.0 to 3.0 μm,
The anti-glare film whose haze value of this anti-glare film is 0.5-3.0%, and the absolute value of the curvature of the maximum curl under 25 degreeC60% RH is 0-18 / m.   2. The antiglare film according to claim 1, wherein the absolute value of the curvature of the maximum curl at 25 ° C. and 60% RH of the antiglare film is 0 to 8 / m.   The antiglare film according to claim 1 or 2, wherein the transparent support is a cellulose ester film containing an esterified compound of a compound having at least one furanose structure or at least one pyranose structure.   The antiglare film according to any one of claims 1 to 3, further comprising a low refractive index layer having a lower refractive index than the antiglare layer on the antiglare layer.   The polarizing plate which used the anti-glare film as described in any one of Claims 1-4 for at least one of the protective films of a polarizing film.   The image display apparatus by which the anti-glare film as described in any one of Claims 1-4 or the polarizing plate of Claim 5 is arrange | positioned on the image display surface. A method for producing an antiglare film having an antiglare layer having a thickness of 2.0 to 5.0 μm on a transparent support having a thickness of 30 to 65 μm,
A curable composition containing the following (A) to (D) and having a solid content ratio of 20 to 40% by mass is applied on the transparent support by 15 to 25 cc / m ² to form a coating film, and then the coating film is irradiated with ultraviolet rays. A method for producing an antiglare film, wherein the antiglare layer is formed by irradiating and curing.
(A) Acrylic compound having an average acrylic equivalent of 100 or less (B) 3 to 15 parts by mass (C) of translucent particles having an average particle diameter of 1.0 to 3.0 μm with respect to 100 parts by mass of the acrylic compound The α-aminoalkylphenone photopolymerization initiator is used in an amount of 0.5 to 5 parts by mass (D) organic solvent based on 100 parts by mass of the acrylic compound.   The production of an antiglare film according to claim 7, wherein the (C) α-aminoalkylphenone photopolymerization initiator is 2-methyl-1- (4-methylthiophenyl) -2-morpholinopropan-1-one. Method. In the ultraviolet irradiation process, the transparent support is wound around a backup roll having a diameter of 400 mm or less, the tension applied in the transport direction of the transparent support is 400 N / m or more, and the film surface temperature of the coating film is 25 ° C. In the following conditions, ultraviolet irradiation is performed by at least three or more ultraviolet irradiation devices, and the peak illumination intensity of ultraviolet irradiation of the first lamp and the second lamp is 5 to 50 mW / cm ² , respectively. The method for producing an antiglare film according to claim 8, wherein the total irradiation amount of ultraviolet rays by the apparatus is 100 mJ / cm ² or more.

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