JP2010085504A - Liquid crystal display - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide an IPS type liquid crystal display which has satisfactory reflection preventing performance while contrast reduction in a bright room is reduced to the minimum and whose display quality and visual field angle are improved with a simple construction. <P>SOLUTION: In the liquid crystal display including a liquid crystal cell having at least a first protective film, a first polarizing film, an optical compensation region, a liquid crystal layer and a pair of substrates interposing the liquid crystal layer, a second polarizing film and a second protective film which are disposed in this order, liquid crystal molecules of the liquid crystal layer are aligned to be parallel to the surfaces of the pair of substrates upon black display, at least an antiglare layer 2 is applied on either of the first protective film and the second protective film, a centerline average roughness (Ra) of the antiglare layer satisfies 0.03 μm<Ra<0.4 μm, an average interval (Sm) of ruggedness satisfies 80 μm<Sm<700 μm and a region (θ(0.5)) of 0°<θ<0.5° occupies 40% or more when an inclined angle θ of the ruggedness is measured. <P>COPYRIGHT: (C)2010,JPO&INPIT

Description

  The present invention relates to a liquid crystal display device, and relates to a ferroelectric liquid crystal display device, an antiferroelectric liquid crystal display device, and an in-plane switching mode liquid crystal that performs display by applying a horizontal electric field to a horizontally aligned nematic liquid crystal. The present invention relates to a display device.

  As a liquid crystal display device, a so-called TN mode is widely used in which a liquid crystal layer in which nematic liquid crystal is twisted is sandwiched between two orthogonal polarizing plates and an electric field is applied in a direction perpendicular to the substrate. In this system, since the liquid crystal rises with respect to the substrate during black display, birefringence occurs due to liquid crystal molecules when viewed from an oblique direction, and light leakage occurs. To solve this problem, a system for optically compensating the liquid crystal cell and preventing this light leakage by using a film in which liquid crystal molecules are hybrid-aligned has been put into practical use. However, even if liquid crystal molecules are used, it is very difficult to completely optically compensate the liquid crystal cell without any problem, and there is a problem that gradation inversion in the lower direction of the screen cannot be suppressed.

  In order to solve such a problem, a liquid crystal display device using a so-called in-plane switching (IPS) mode in which a lateral electric field is applied to the liquid crystal, or a liquid crystal having a negative dielectric anisotropy is vertically aligned in the panel. A vertical alignment (VA) mode in which alignment is divided by protrusions and slit electrodes has been proposed and put into practical use. In recent years, these panels have been widely used for TV applications, and accordingly, the brightness of the screen has been greatly improved. For this reason, a slight light leakage in the diagonally oblique incident direction at the time of black display, which has not been considered as a problem in these operation modes, has become apparent as a cause of the deterioration in display quality.

  As a means for improving the color tone and the viewing angle of black display, disposing an optical compensation material having birefringence characteristics between a liquid crystal layer and a polarizing plate is also studied in the IPS mode (for example, see Patent Document 1).

On the other hand, in these liquid crystal display devices, in order to prevent reflection of an image due to reflection of external light, an antiglare film is disposed on the outermost surface of the display, thereby increasing the added value of the liquid crystal display. Yes.
As the antiglare film, an antiglare film having internal scattering properties in addition to surface scattering is known (see, for example, Patent Document 2).

  However, when the conventional anti-glare film is applied to an IPS mode liquid crystal display device in which the above-described conventional techniques are combined, that is, optical compensation is performed, the reflection of an image due to reflection of external light can be prevented. However, the inventors have clarified that light leakage in a diagonally oblique incident direction is higher than that before application of the antiglare film.

JP-A-10-307291 Japanese Patent No. 3515401

  The present invention has been made in view of the above problems, and is capable of suppressing light leakage in a diagonally diagonal direction while preventing reflection of an image due to reflection of external light, and having a simple configuration and display. An object of the present invention is to provide an IPS liquid crystal display device in which not only the quality but also the viewing angle is remarkably improved.

  In addition, the present invention has been made in view of the above problems, and provides an IPS liquid crystal display device that has excellent antireflection performance, has a simple configuration, and has a remarkably improved viewing angle as well as display quality. The purpose is to provide.

Means for solving the above problems are as follows.
1.
At least a first protective film, a first polarizing film, an optical compensation region, a liquid crystal cell having a liquid crystal layer and a pair of substrates sandwiching the liquid crystal layer, a second polarizing film, and a second protective film A liquid crystal display device in which the liquid crystal molecules of the liquid crystal layer are aligned in parallel to the surfaces of the pair of substrates at the time of black display, and at least one of the first protective film and the second protective film Has an antiglare layer,
Of the antiglare layer,
The center line average roughness (Ra) is 0.03 μm <Ra <0.4 μm,
The average interval (Sm) of the irregularities is 80 μm <Sm <700 μm,
A liquid crystal display device in which an area of 0 ° <θ <0.5 ° (θ (0.5)) occupies 40% to 98% at an inclination angle θ of the unevenness.
2.
2. The antiglare layer contains at least one kind of translucent particles, and the average particle diameter of the translucent particles is 0.01 to 4.0 μm larger than the average film thickness of the antiglare layer. Liquid crystal display device.
3.
3. The liquid crystal display device according to 1 or 2 above, wherein the addition amount of the translucent particles is 0.01 to 1% by mass with respect to the total solid content of the antiglare layer.
4.
4. The liquid crystal display device according to any one of 1 to 3, wherein the translucent particles have an average particle size of 3 μm to 15 μm.
5.
5. The liquid crystal display device according to any one of 1 to 4, wherein a low refractive index layer having a refractive index lower than that of the antiglare layer is provided on the surface of the antiglare layer.
6.
6. The liquid crystal display device according to any one of 1 to 5, wherein the optical compensation region includes at least one retardation region that satisfies any of the following formulas (A) to (D).
(A) 100 nm ≦ Re ≦ 400 nm and −50 nm ≦ Rth ≦ 50 nm
(B) 60 nm ≦ Re ≦ 200 nm and 30 nm ≦ Rth ≦ 100 nm
(C) 0 nm ≦ Re ≦ 20 nm and −400 nm ≦ Rth ≦ −50 nm
(D) 30 nm ≦ Re ≦ 150 nm and 100 nm ≦ Rth ≦ 400 nm
(Here, Re is in-plane retardation, and Rth is retardation in the thickness direction.)
7.
7. The liquid crystal display device according to 6, wherein the first retardation region satisfying any one of the formulas (A) to (D) is a cellulose ester film.
8.
8. The liquid crystal display device according to 6 or 7, wherein the optical compensation region includes a first retardation region that satisfies the formula (A), and a value Nz of the first retardation region is 0.45 to 0.55.
9.
The optical compensation region includes a first retardation region and a second retardation region;
The in-plane retardation Re of the first retardation region is 60 nm to 200 nm,
The thickness direction retardation Rth of the first retardation region is 30 nm to 100 nm,
In-plane retardation Re of the second retardation region is 0 nm to 20 nm,
8. The liquid crystal display device according to any one of 1 to 7, wherein a retardation Rth in the thickness direction of the second retardation region is −300 nm to −100 nm.
10.
The first polarizing film, the first retardation region, the second retardation region, and the liquid crystal cell are provided in this order, and the slow axis of the first retardation region is that of the first polarizing film. 10. The liquid crystal display device according to 9 above, which is substantially perpendicular to the absorption axis.
11.
The first polarizing film, the second retardation region, the first retardation region, and the liquid crystal cell are provided in this order, and the slow axis of the first retardation region is that of the first polarizing film. 10. The liquid crystal display device according to 9 above, which is substantially parallel to the absorption axis.
12.
The optical compensation region includes a first retardation region and a second retardation region;
The in-plane retardation Re of the first retardation region is 30 nm to 150 nm,
The thickness direction retardation Rth of the first retardation region is 100 nm to 400 nm,
In-plane retardation Re of the second retardation region is 0 nm to 20 nm,
The retardation Rth in the thickness direction of the second retardation region is −400 nm to −80 nm, and the absorption axis of the first polarizing film is perpendicular to the slow axis direction of the liquid crystal molecules during black display. 8. A liquid crystal display device according to any one of 7 above.
13.
The first polarizing film, the first retardation region, the second retardation region, and the liquid crystal cell are provided in this order, and the slow axis of the first retardation region is that of the first polarizing film. 13. The liquid crystal display device as described in 12 above, which is substantially perpendicular to the absorption axis.
14.
The first polarizing film, the second retardation region, the first retardation region, and the liquid crystal cell are provided in this order, and the slow axis of the first retardation region is that of the first polarizing film. 13. The liquid crystal display device as described in 12 above, which is substantially parallel to the absorption axis.
15.
The liquid crystal display device according to any one of the above 9 to 14, wherein the second retardation region has a retardation layer containing a rod-like liquid crystal compound that is substantially vertically aligned.
16.
16. The liquid crystal display device according to any one of 1 to 15 above, wherein a protective film is provided between the second polarizing film and the substrate, and the retardation Rth in the thickness direction of the protective film is −50 nm to 40 nm.
17.
The liquid crystal display device according to any one of 1 to 16, further comprising a protective film between the second polarizing film and the substrate, wherein the protective film is a cellulose acylate film, a norbornene film, or an acrylic film. .

  According to the present invention, it is possible to improve the viewing angle while minimizing the decrease in bright room contrast and preventing the reflection of external light on the liquid crystal display surface.

  Hereinafter, the present invention will be described in detail. In the present specification, a numerical range represented by using “to” means a range including numerical values described before and after “to” as a lower limit value and an upper limit value.

  In the present specification, numerical values and numerical ranges indicating optical characteristics and the like are to be interpreted as numerical values or numerical ranges including generally allowable errors for liquid crystal display devices and members used therefor. . Regarding the angle, in this specification, “45 °”, “parallel” or “orthogonal” means that the angle is within a range of strictly less than ± 5 °. The error from the exact angle is preferably less than 4 °, more preferably less than 3 °. Regarding the angle, “+” means the clockwise direction, and “−” means the counterclockwise direction. Further, the “slow axis” means a direction in which the refractive index is maximized. The “visible light region” means 380 to 780 nm. Further, the measurement wavelength of the refractive index is a value at λ = 590 nm in the visible light region unless otherwise specified.

  Further, in this specification, the “polarizing plate” is cut into a size to be incorporated into a long polarizing plate and a liquid crystal device unless otherwise specified (in this specification, “cutting” includes “punching” and The term “includes“ cutout ”and the like” is used to include both polarizing plates. In this specification, “polarizing film” and “polarizing plate” are distinguished from each other. “Polarizing plate” means a laminate having a transparent protective film for protecting the polarizing film on at least one side of the “polarizing film”. It shall be.

In this specification, Re (λ) and Rth (λ) represent in-plane retardation and retardation in the thickness direction at the wavelength λ, respectively. Re (λ) is measured by making light having a wavelength of λ nm incident in the normal direction of the film in KOBRA 21ADH or WR (manufactured by Oji Scientific Instruments).
In selecting the measurement wavelength λnm, the wavelength selection filter can be exchanged manually, or the measured value can be converted by a program or the like.
When the film to be measured is represented by a uniaxial or biaxial refractive index ellipsoid, Rth (λ) is calculated by the following method.
Rth (λ) is Re (λ), with the in-plane slow axis (determined by KOBRA 21ADH or WR) as the tilt axis (rotation axis) (if there is no slow axis, any in-plane film The light of wavelength λ nm is incident from each of the inclined directions in steps of 10 degrees from the normal direction to 50 degrees on one side with respect to the film normal direction (with the direction of the rotation axis as the rotation axis). KOBRA 21ADH or WR is calculated based on the measured retardation value, the assumed value of the average refractive index, and the input film thickness value.

In the above case, in the case of a film having a direction in which the retardation value is zero at a certain tilt angle with the in-plane slow axis from the normal direction as the rotation axis, retardation at a tilt angle larger than the tilt angle. The value is calculated by KOBRA 21ADH or WR after changing its sign to negative.
The retardation value is measured from two inclined directions with the slow axis as the tilt axis (rotation axis) (if there is no slow axis, the arbitrary direction in the film plane is the rotation axis). Based on the value, the assumed value of the average refractive index, and the input film thickness value, Rth can also be calculated from the following formulas (I) and (II).
Formula (I)

Formula (II)
Rth = {(nx + ny) / 2−nz} × d
In the formula, Re (θ) represents a retardation value in a direction inclined by an angle θ from the normal direction.
Nx represents the refractive index in the slow axis direction in the plane, ny represents the refractive index in the direction perpendicular to nx in the plane, nz represents the refractive index in the direction perpendicular to nx and ny, and d Represents the film thickness.

When the film to be measured is a film that cannot be expressed by a uniaxial or biaxial refractive index ellipsoid, that is, a film without a so-called optical axis, Rth (λ) is calculated by the following method.
Rth (λ) is the above-mentioned Re (λ), and the in-plane slow axis (determined by KOBRA 21ADH or WR) is the tilt axis (rotary axis), and −50 degrees to +50 degrees with respect to the film normal direction. Measured at 11 points by making light of wavelength λ nm incident from each tilted direction in 10 degree steps, and based on the measured retardation value, assumed value of average refractive index, and input film thickness value KOBRA 21ADH or WR is calculated.
In the above measurement, as the assumed value of the average refractive index, values in the polymer handbook (John Wiley & Sons, Inc.) and catalogs of various optical compensation films can be used.
Moreover, about the thing whose average refractive index value is not known, it can measure with an Abbe refractometer. Examples of the average refractive index values of main optical compensation films are as follows:
Cellulose acylate (1.48), cycloolefin polymer (1.52), polycarbonate (1.59), polymethyl methacrylate (1.49), and polystyrene (1.59).
The KOBRA 21ADH or WR calculates nx, ny, and nz by inputting the assumed average refractive index and the film thickness. Nz = (nx−nz) / (nx−ny) is further calculated from the calculated nx, ny, and nz.

[Liquid Crystal Display]
The liquid crystal display device of the present invention includes at least a first protective film, a first polarizing film, an optical compensation region, a liquid crystal cell having a liquid crystal layer and a pair of substrates sandwiching the liquid crystal layer, a second polarizing film, And a second protective film in this order, and a liquid crystal display device in which liquid crystal molecules of the liquid crystal layer are aligned in parallel to the surfaces of the pair of substrates during black display, wherein the first protective film or the second protective film 2 At least one of the protective films has an antiglare layer,
Of the antiglare layer,
The center line average roughness (Ra) is 0.03 μm <Ra <0.4 μm,
The average interval (Sm) of the irregularities is 80 μm <Sm <700 μm,
The liquid crystal display device has an area where 0 ° <θ <0.5 ° (θ (0.5)) occupies 40% to 98% at the inclination angle θ of the unevenness.

  When a conventional anti-glare layer is applied to the surface of an IPS mode liquid crystal display device, even if the liquid crystal display device performs optical compensation, leakage in a diagonally diagonal direction occurs. It has been clarified by the present inventors that the reason for the light leakage is as follows.

  That is, in a conventional liquid crystal display device in which an antiglare layer is laminated, a part of light incident at a high angle from the backlight side is refracted by the surface irregularities of the antiglare layer, and is emitted at a lower angle and visually recognized. On the other hand, the light leakage in the diagonally diagonal direction increases as the angle increases. Therefore, when a conventional anti-glare layer is applied, a component incident at a wider angle is included and emitted, and thus leakage light in a diagonally diagonal direction is generated. On the other hand, when the antiglare property is lowered, refraction due to surface irregularities is reduced and light leakage in a diagonally diagonal direction is reduced, but the reflection of the image is strong and the visibility is deteriorated. In other words, it was not possible to simultaneously solve the light leakage in the diagonal direction and the reflection of the image.

On the other hand, it has been found that the above problems can be solved simultaneously by applying the above-described antiglare layer having the characteristics of the present invention (hereinafter sometimes referred to as the antiglare layer of the present invention). It came to. The antiglare layer of the present invention has less uneven portions and more flat portions than the conventional antiglare layer (FIG. 4). By using such an antiglare layer, light leakage in a diagonally diagonal direction and image reflection can be solved simultaneously. The reason is presumed to be based on the following reasons. Increasing the planar portion of the antiglare layer can reduce refraction during emission, reduce light incident at a wide angle and exit at a low angle, and suppress light leakage in a diagonally diagonal direction. . On the other hand, since the amount of scattered light in the direction close to the mirror surface direction can be increased, the image is blurred and less noticeable.
Further, even when the antiglare layer of the present invention was applied to the TN mode, the light leakage reduction effect in the oblique direction was not observed. Therefore, it was found that the present invention is the first effect obtained by combining the IPS mode liquid crystal display device in which light leakage in the oblique direction is improved structurally, optical compensation, and the antiglare layer of the present invention.

  Furthermore, in the system in which the low refractive index layer is laminated on the antiglare layer of the present invention, since there are many plane portions of the antiglare layer, it is low compared with the conventional antiglare layer (schematically shown in FIG. 3). The refractive index layer can be applied uniformly (schematically shown in FIG. 4), and the surface is mirror-reflected with uniformity (schematically shown in FIG. 2) similar to a low-refractive layer applied on a flat surface. The rate can be reduced. Therefore, the structure in which the low refractive index layers are laminated is a preferred embodiment of the present invention.

<Anti-glare layer>
[Configuration of antiglare layer]
The antiglare layer in the present invention has at least one antiglare layer comprising fine particles and a binder on a transparent support. The antiglare film of the present invention will be described with reference to FIG.

  The antiglare film of the present invention in FIG. 1 has at least one antiglare layer (2) on the transparent support (1). The outermost layer preferably has a low refractive index layer (5) having a refractive index lower than that of the adjacent antiglare layer (2).

[Anti-glare layer]
As a method for imparting antiglare properties, a method of laminating and forming a mat-shaped shaping film having fine irregularities on the surface as described in JP-A-6-16851, as described in JP-A-2000-206317 As described above, the method of forming by curing shrinkage of ionizing radiation curable resin due to the difference in ionizing radiation dose, and the mass ratio of good solvent to translucent resin decreases by drying as described in JP-A-2000-338310. A method of forming unevenness on the surface of the coating film by solidifying the light-transmitting fine particles and the light-transmitting resin while gelling, and applying surface unevenness by external pressure as described in JP-A-2000-275404 A method, a method of imparting surface irregularities by external pressure as described in JP-A-2000-275404, and a method described in JP-A-2005-195819. In addition, a method of forming surface irregularities by utilizing phase separation in the process of evaporation of a solvent from a mixed solution of a plurality of polymers, etc. are known, and these are used to form an antiglare layer in the film of the present invention. Known methods can be used.

The antiglare layer that can be used in the present invention is preferably composed of a binder capable of imparting hard coat properties and translucent particles for imparting antiglare properties. It is preferable that the layer has irregularities formed on the surface by protrusions formed by aggregates of the particles.
Moreover, it is preferable that an anti-glare layer is formed using the coating material for anti-glare layer formation containing a binder formation material, translucent particle | grains, and a solvent.

  And the glare-proof layer formed using the coating material for glare-proof layer formation consists of a binder and the translucent particle disperse | distributed in the binder, and it is preferable to have antiglare property and hard-coat property.

(Translucent particles)
As one of the preferred embodiments of the present invention, the antiglare layer contains at least one kind of the light transmitting particles for imparting antiglare properties, and the average particle diameter of the light transmitting particles is that of the antiglare layer. 0.01 to 4.0 μm larger than the average film thickness is preferable in terms of imparting antiglare properties, and the ratio of the antiglare property and the flat portion of the film surface is increased, and the thin film interference layer is uniformly laminated. Is preferably 0.5 to 3.5 μm larger, and most preferably 1.0 to 3.0 μm larger. Moreover, when the average particle diameter of translucent particle | grains is 4 micrometers or less, it is preferable that it is 0.1-2.5 micrometers larger, and it is most preferable that it is 0.1-2.0 micrometers larger.
The average film thickness of the antiglare layer is calculated from an average value obtained by observing the cross section of the film with an electron microscope and measuring 30 film thicknesses randomly.

  It is preferable that one convex portion of the antiglare layer is substantially formed by 5 or less translucent particles, and that the convex portion is substantially formed by one translucent particle. preferable. Here, “substantially” means that 90% or more of the convex portions defined above satisfy a preferable mode.

  In the present invention, the particle size distribution of the translucent particles used is a monodisperse particle, that is, a particle having a uniform particle diameter, from the viewpoint of control of haze value and diffusibility, and uniformity of the coated surface. Preferably there is. The CV value representing the uniformity of the particle diameter is preferably 0 to 10%, more preferably 0 to 8%, and still more preferably 0 to 5%. Further, when a particle having a particle size of 20% or more than the average particle size is defined as a coarse particle, the proportion of the coarse particle is preferably 1% or less of the total number of particles, more preferably 0.1% or less. Yes, more preferably 0.01% or less. The translucent particles having such a particle size distribution are also effective means of classification after the preparation or synthesis reaction. By increasing the number of times of classification or increasing the degree thereof, particles having a desired distribution can be obtained. be able to. It is preferable to use a method such as an air classification method, a centrifugal classification method, a sedimentation classification method, a filtration classification method, or an electrostatic classification method for classification. The average particle diameter of the translucent particles is calculated from an average value of 100 observed particle diameters obtained by observing the translucent particles with an optical microscope.

  The addition amount of the translucent particles having an average particle diameter larger than the average film thickness of the antiglare layer is 0.01 to 1% by mass with respect to the total solid content to roughen the unevenness density. This is preferable in that the ratio of the flat portion on the film surface is increased and the thin film interference layer is uniformly laminated. More preferably, it is 0.1-1 mass%, More preferably, it is 0.1-0.7 mass%, Most preferably, it is 0.1-0.45 mass%.

  In this invention, it is preferable that the average particle diameter of translucent particle | grains is 3 micrometers-15 micrometers. It is preferably 5 μm to 12 μm, and most preferably 6 μm to 10 μm. If the particle size is less than 3 μm, the film thickness of the antiglare layer becomes thin and sufficient pencil hardness cannot be obtained. On the other hand, if the thickness is larger than 15 μm, the film thickness is large and the problem of curling occurs.

The number of translucent particles having an average particle size larger than the average film thickness of the antiglare layer per unit area in the antiglare layer is preferably 10 to 1500 / mm ² . More preferably 10 to 400 pieces / mm ^2, and most preferably 10 to 100 / mm ^2. The number of translucent particles can be calculated from an average value obtained by observing 10 fields in a 500 μm × 500 μm range with an optical microscope and counting each number.

The anti-glare layer in the present invention is different from the conventionally known anti-glare layer, and the anti-glare property is caused by particles having an average particle diameter of 0.01 to 1% by mass which is larger than the average film thickness of the anti-glare layer. Therefore, when the thin film layer is laminated on the antiglare layer, unevenness due to unevenness hardly occurs and a low reflectance can be realized. it can.
At this time, since the particles protrude from the antiglare layer by at least 0.01 to 4.0 μm and exhibit antiglare properties, the antiglare properties are not impaired even if there are many flat portions.

In the present invention, the center line average roughness (Ra) is 0.03 μm <Ra <0.40 μm. In addition to the antiglare property, it is 0.05 μm in consideration of glare and surface whitening when external light is reflected. <Ra <0.30 μm is preferable, 0.05 <Ra <0.25 μm is more preferable, and 0.05 <Ra <0.15 μm is most preferable.
In addition, the average unevenness interval (Sm) is 80 μm <Sm <700 μm, and in order to increase the ratio of the antiglare property and the flat portion of the film surface and to uniformly laminate the thin film interference layer, the average of the unevenness The interval (Sm) is preferably 150 μm <Sm <700 μm, and most preferably 200 μm <Sm <600 μm.

  When the center line average roughness (Ra) of the antiglare film is 0.03 μm or less, the surface unevenness is so small that the antiglare property cannot be sufficiently obtained. When the thickness is 0.4 μm or more, problems such as glare, whitening of the surface when external light is reflected, and a problem of reduced interference ability due to uneven film thickness of the thin film layer according to the unevenness occur.

  When the average interval (Sm) of the unevenness is 80 μm or less, there is a structure with few flat portions on the surface unevenness, which causes a problem of reduced interference ability due to uneven film thickness when the thin film layer is applied. When it is 700 μm or more, the structure has a very large number of flat portions on the surface, and sufficient antiglare properties cannot be obtained.

  In the present invention, the region (θ (0.5)) where the inclination angle θ of the unevenness is 0 ° <θ <0.5 ° needs to occupy 40% to 98%, and is 50% to 98%. Is preferable, 60% to 98% is more preferable, and 70% to 95% is most preferable.

  When θ (0.5) is less than 40%, the interference ability is reduced due to the non-uniform thickness of the thin film layer corresponding to the unevenness. On the other hand, if it exceeds 98%, a sufficient antiglare effect cannot be obtained. When the integrated reflectance is 1.5% or less, an antireflection film with good black tightening can be obtained.

  In the antiglare layer of the present invention, θ (0.5) (relatively flat region on the coating film surface), which has been difficult with conventional antiglare layers, is kept at 40% or more, 80 μm <Sm <700 μm. Sufficient antiglare properties can be imparted, and when a plurality of thin film layers are laminated by a coating method, both sufficient antiglare properties and low reflectance can be achieved.

(Inclination angle θ)
The optical film of the present invention has a fine uneven structure on the surface. In the present invention, the distribution of the inclination angle θ is determined by the following method. That is, assuming that the apex of a triangle having an area of 0.5 to 2 square micrometers is a transparent film substrate surface (support surface), three perpendicular lines extending vertically upward from that point intersect with the film surface. The angle formed by the normal of the triangular surface formed and a perpendicular extending vertically upward from the support surface is defined as the surface inclination angle, and an area of 250,000 square micrometers (0.25 square millimeters) or more on the substrate The inclination angle distribution at all measurement points when measuring by dividing into triangles is examined.

  A method for measuring the tilt angle will be described in detail with reference to FIG. The film is divided into meshes having an area on the support surface of 0.5 to 2 square micrometers (see FIG. 10A). FIG. 10B is a diagram in which three points of the divided mesh are extracted. A perpendicular line is extended vertically upward from three points on the support, and points where the three points intersect the surface are designated as A, B, and C. An angle θ formed by a normal line DD ′ of the triangle ABC plane and a perpendicular line OO ′ extending vertically upward from the support is defined as an inclination angle. FIG. 10C is a cross-sectional view of the film taken along the plane P including the point O′DD ′. A line segment EF is an intersection line between the triangle ABC and the plane P. The measurement area is preferably 250,000 square micrometers (0.25 square millimeters) or more on the support, and this surface is divided into triangles on the support and measured to determine the inclination angle. There are several devices to measure, but an example will be described. A case will be described in which an SXM520-AS150 model manufactured by Micromap (USA) is used as the apparatus. For example, when the objective lens is 10 times, the measurement unit of the tilt angle is 0.8 square micrometers, and the measurement range is 500,000 square micrometers (0.5 square millimeters). If the magnification of the objective lens is increased, the measurement unit and the measurement range are reduced accordingly. The measurement data can be analyzed using software such as MAT-LAB, and the tilt angle distribution can be calculated. A frequency θ (0.5) at an inclination angle of 0 to 0.5 ° is calculated from the obtained inclination angle distribution. Measurements are taken at five locations at different locations, and the average value is taken.

(Integral reflectance)
The back surface of the optical film, that is, the side opposite to the low refractive index layer is roughened with sandpaper and then treated with black ink to eliminate the back surface reflection. It is attached to an integrating sphere of 550 (manufactured by JASCO Corporation), the reflectance (integrated reflectance) is measured in the wavelength region of 380 to 780 nm, and the average reflectance of 450 to 650 nm is calculated.

(Evaluation of surface shape)
The surface shape of the optical film is evaluated based on JIS B-0601 (1994) with respect to the arithmetic average roughness (Ra) and average interval (Sm) of the surface irregularities by using a surf coder MODEL SE-3F manufactured by Kosaka Laboratory. . Regarding Sm, the measurement length at the time of measurement was 8 mm, and the cut-off value was 0.8 mm.

(Fine particles)
About the kind of fine particle (translucent particle), it is preferable to satisfy | fill the value of the said particle size and the internal haze of the glare-proof layer mentioned later, and a convex part is formed substantially by one fine particle. Therefore, it is preferable to select fine particles having good dispersibility.

  As fine particles having good dispersibility, translucent organic resin particles such as polymethyl methacrylate fine particles and polymethyl methacrylate / polystyrene copolymer fine particles are preferable. The polymethyl methacrylate ratio in the copolymer fine particles is preferably 40% by mass or more from the viewpoint of dispersibility.

  In the case of using the above fine particles, in order to prevent dispersion of particles in the binder or coating solution and to prevent sedimentation, inorganic fillers such as silica that do not cause visible light scattering, organic compounds (even monomers) A dispersing agent such as a polymer) may be added.

  In addition, when adding an inorganic filler, it is effective for the precipitation prevention of microparticles | fine-particles, so that the addition amount increases, However, It is preferable to use in the range which does not have a bad influence on the transparency of a coating film. Therefore, it is preferable that an inorganic filler having a particle size of 0.5 μm or less is contained in an amount of about 0.1% by mass so as not to impair the transparency of the coating film with respect to the binder. The dispersant such as an organic compound is preferably added in an amount of 0.1 to 20% by mass with respect to the fine particles. More preferably, it is 0.1-15 mass%, Most preferably, it is 0.5-10 mass%. If it is 0.1% by mass or more, the effect of addition to the dispersion stability appears, and if it is 20% by mass or less, the components that do not contribute to the dispersion stability increase and problems such as bleeding out do not occur.

  As described above, the surface of fine particles used as an additive may be surface-treated for dispersion stability and prevention of settling in a binder or coating solution. The type of the surface treatment agent is appropriately selected depending on the binder to be used and the solvent in the coating solution. As a surface treatment amount, it is preferable to add 0.1 to 30% by mass with respect to fine particles. More preferably, it is 1-25 mass%, Most preferably, it is 3-20 mass%. If it is 0.1% by mass or more, the amount of surface treatment for dispersion stability will not be insufficient, and if it is 30% by mass or less, components that do not contribute to the surface treatment increase and problems such as bleed out may occur. It is preferable because it is not present.

  In the present invention, the particle size distribution of the fine particles used is a monodisperse particle, that is, a particle having a uniform particle diameter, from the viewpoint of control of haze value and diffusibility, and uniformity of the coated surface. Is preferred. The CV value representing the uniformity of the particle diameter is preferably 0 to 10%, more preferably 0 to 8%, and still more preferably 0 to 5%. Further, when a particle having a particle size of 20% or more than the average particle size is defined as a coarse particle, the proportion of the coarse particle is preferably 1% or less of the total number of particles, more preferably 0.1% or less. Yes, more preferably 0.01% or less. Fine particles having such a particle size distribution are also effective means of classification after preparation or synthesis reaction, and particles having a desired distribution can be obtained by increasing the number of classifications or increasing the degree of classification. . It is preferable to use a method such as an air classification method, a centrifugal classification method, a sedimentation classification method, a filtration classification method, or an electrostatic classification method for classification. The average particle diameter of the fine particles is calculated from an average value of the diameters of 100 particles observed by observing the fine particles with an electron microscope.

Further, two or more kinds of fine particles having different average particle diameters may be used in combination in order to obtain necessary light scattering properties. In this case, the average particle diameter of at least one kind of particles is 0.01 to 4.0 μm larger than the average film thickness of the antiglare layer, and the average particle diameter is 0.01 to 4.mu. It is preferable that the addition amount of the 0 μm larger particles is 0.01 to 1% by mass with respect to the solid content of the antiglare layer. When there are two or more kinds of particles having an average particle diameter of 0.01 to 4.0 μm larger than the average film thickness of the antiglare layer, the total addition amount is 0.01 to 1 with respect to the solid content of the antiglare layer. It is preferable that it is mass%.
By making the addition amount of the particles of the antiglare layer in the above range, the plane portion can be increased, incident from a wide angle, refracted on the surface of the antiglare layer, and reducing the light emitted at a low angle. And light leakage in a diagonally diagonal direction can be prevented.

(binder)
The binder of the antiglare layer in the present invention preferably contains one or both of a thermosetting resin and an ionizing radiation curable compound and is formed by curing.

  The antiglare layer in the present invention is preferably a layer formed by a crosslinking reaction or a polymerization reaction of an ionizing radiation curable compound. That is, as a binder, a coating composition containing an ionizing radiation curable polyfunctional monomer or polyfunctional oligomer is coated on a transparent support, and the polyfunctional monomer or polyfunctional oligomer is formed by a crosslinking reaction or a polymerization reaction. . The functional group of the ionizing radiation-curable polyfunctional monomer or polyfunctional oligomer is preferably a light (ultraviolet ray), electron beam, or radiation polymerizable group, and among them, a photopolymerizable functional group is preferable. Examples of the photopolymerizable functional group include unsaturated polymerizable functional groups such as a (meth) acryloyl group, a vinyl group, a styryl group, and an allyl group. Among them, a (meth) acryloyl group is preferable.

  Specific examples of the photopolymerizable polyfunctional monomer having a photopolymerizable functional group include alkylenes such as neopentyl glycol di (meth) acrylate, 1,6-hexanediol di (meth) acrylate, and propylene glycol di (meth) acrylate. (Meth) acrylic acid diesters of glycol; of polyoxyalkylene glycols such as triethylene glycol di (meth) acrylate, dipropylene glycol di (meth) acrylate, polyethylene glycol di (meth) acrylate and polypropylene glycol di (meth) acrylate (Meth) acrylic acid diesters; of polyhydric alcohols such as pentaerythritol di (meth) acrylate, pentaerythritol tri (meth) acrylate, trimethylolpropane tri (meth) acrylate Of (meth) acrylic polyesters; 2,2-bis {4- (acryloxy / diethoxy) phenyl} propane, ethylene oxide or propylene oxide adducts such as 2-2-bis {4- (acryloxy / polypropoxy) phenyl} propane (Meth) acrylic acid diesters; Furthermore, epoxy (meth) acrylates, urethane (meth) acrylates, and polyester (meth) acrylates are also preferably used as the photopolymerizable polyfunctional monomer.

  Among these, esters of polyhydric alcohol and (meth) acrylic acid are preferable. More preferably, a polyfunctional monomer having 3 or more (meth) acryloyl groups in one molecule is preferable. Specifically, trimethylolpropane tri (meth) acrylate, trimethylolethane tri (meth) acrylate, 1,2,4-cyclohexanetetra (meth) acrylate, pentaglycerol triacrylate, pentaerythritol tetra (meth) acrylate, penta Erythritol tri (meth) acrylate, dipentaerythritol triacrylate, dipentaerythritol pentaacrylate, dipentaerythritol tetra (meth) acrylate, dipentaerythritol hexa (meth) acrylate, tripentaerythritol triacrylate, tripentaerythritol hexatriacrylate, etc. Is mentioned.

  As the polyfunctional monomer binder, monomers having different refractive indexes can be used to control the refractive index of each layer. Examples of particularly high refractive index monomers include bis (4-methacryloylthiophenyl) sulfide, vinyl naphthalene, vinyl phenyl sulfide, 4-methacryloxyphenyl-4'-methoxyphenyl thioether and the like. Further, for example, dendrimers described in JP-A-2005-76005 and JP-A-2005-36105 and norbornene ring-containing monomers as described in JP-A-2005-60425 can also be used. Two or more types of these multifunctional monomers and multifunctional oligomer binders used as binders may be used in combination.

  Here, the refractive index of the antiglare layer can be quantitatively evaluated by directly measuring it with an Abbe refractometer or by measuring a spectral reflection spectrum or a spectral ellipsometry. The refractive index of the fine particles is measured by measuring the turbidity by dispersing an equal amount of fine particles in a solvent in which the refractive index is changed by changing the mixing ratio of two types of solvents having different refractive indexes. It is measured by measuring the refractive index of the solvent with an Abbe refractometer.

  Polymerization of the binder having these ethylenically unsaturated groups can be performed by irradiation with ionizing radiation or heating in the presence of a photo radical initiator or a thermal radical initiator. In the polymerization reaction of the photopolymerizable polyfunctional monomer or polyfunctional oligomer, it is preferable to use a photopolymerization initiator. As the photopolymerization initiator, a photoradical polymerization initiator and a photocationic polymerization initiator are preferable, and a photoradical polymerization initiator is particularly preferable.

  In the present invention, a polymer or a crosslinked polymer can be used in combination as a binder. The crosslinked polymer preferably has an anionic group. The polymer having a crosslinked anionic group has a structure in which the main chain of the polymer having an anionic group is crosslinked.

  Examples of the polymer main chain include polyolefin (saturated hydrocarbon), polyether, polyurea, polyurethane, polyester, polyamine, polyamide and melamine resin. A polyolefin main chain, a polyether main chain and a polyurea main chain are preferable, a polyolefin main chain and a polyether main chain are more preferable, and a polyolefin main chain is most preferable.

For the purpose of controlling the refractive index of the antiglare layer, the binder of the antiglare layer has a high refractive index monomer or inorganic particles that do not cause visible light scattering such as ZrO ₂ , TiO ₂ , and SiO ₂ , that is, an average particle size. Inorganic particles of 100 nm or less, or both of them can be added. In addition to the effect of controlling the refractive index, the inorganic particles also have the effect of suppressing cure shrinkage due to the crosslinking reaction. In the present invention, a polymer formed by polymerizing the polyfunctional monomer and / or the high refractive index monomer after the antiglare layer is formed, and the inorganic particles dispersed therein are referred to as a binder.

Next, the internal haze of the present invention will be described in detail.
Add a few drops of silicone oil to the front and back of the anti-glare film, and use 2 sheets of 1 mm thick glass plates ("Micro Slide Glass Part No. S9111", made by MATSUNAMI) from the front and back to completely A value obtained by measuring haze according to JIS-K7136 with the glass plate and the obtained antiglare film adhered, and subtracting the haze measured by sandwiching only silicone oil between two separately measured glass plates. Was calculated as the internal haze of the film.

  The internal haze of the antiglare film of the present invention is preferably 0.1% to 25% from the viewpoint that no glare of the liquid crystal panel is generated and the contrast is not lowered, and more preferably 1% to 20%. Yes, particularly preferably from 3% to 15%.

  The refractive index of the antiglare layer is preferably 1.45 to 1.6, more preferably 1.46 to 1.57, and particularly preferably 1.47 to 1.55.

[Low refractive index layer]
In the present invention, a low refractive index layer can be provided outside the antiglare layer, that is, on the side farther from the transparent support. By having a low refractive index layer, it is possible to impart an antireflection function to the antiglare film and further improve the antiglare property. The refractive index of the low refractive index layer is preferably set lower than the refractive index of the antiglare layer. When the difference in refractive index between the low refractive index layer and the antiglare layer is too small, the antireflection property is lowered. The refractive index difference between the low refractive index layer and the antiglare layer is preferably from 0.01 to 0.30, and more preferably from 0.05 to 0.20.

The low refractive index layer can be formed using a low refractive index material. A low refractive index binder can be used as the low refractive index material. Further, the low refractive index layer can be formed by adding fine particles to the binder.
Moreover, the composition for low refractive index layer formation can also contain the organosilane compound mentioned later.

  As the low refractive index binder, a fluorine-containing copolymer can be preferably used. The fluorinated copolymer preferably has a structural unit derived from a fluorinated vinyl monomer and a structural unit for imparting crosslinkability.

(Fluorine-containing copolymer)
Examples of the fluorinated vinyl monomer mainly constituting the fluorinated copolymer include fluoroolefins (eg, fluoroethylene, vinylidene fluoride, tetrafluoroethylene, hexafluoropropylene, etc.), a part of (meth) acrylic acid or a fully fluorinated alkyl. Ester derivatives {for example, “Biscoat 6FM” (trade name), Osaka Organic Chemical Industry Co., Ltd., “R-2020” (trade name), manufactured by Daikin Industries, Ltd., etc.}, fully or partially fluorinated vinyl ethers, etc. Of these, perfluoroolefins are preferable, and hexafluoropropylene is particularly preferable from the viewpoint of refractive index, solubility, transparency, availability, and the like.

  Increasing the composition ratio of these fluorinated vinyl monomers can lower the refractive index, but the film strength tends to decrease. In the present invention, the fluorine-containing vinyl monomer is preferably introduced so that the fluorine content of the copolymer is 20 to 60% by mass, more preferably 25 to 55% by mass, and particularly preferably 30 to 50%. This is a case of mass%.

Examples of the structural unit for imparting crosslinking reactivity include units represented by the following (A), (B), and (C).
(A): a structural unit obtained by polymerization of a monomer having a self-crosslinkable functional group in the molecule in advance such as glycidyl (meth) acrylate or glycidyl vinyl ether,
(B): a monomer having a carboxyl group, a hydroxy group, an amino group, a sulfo group or the like {for example, (meth) acrylic acid, methylol (meth) acrylate, hydroxyalkyl (meth) acrylate, allyl acrylate, hydroxyethyl vinyl ether, hydroxybutyl vinyl ether , Maleic acid, crotonic acid, etc.}
(C): A group having a crosslinkable functional group separately from a group that reacts with the functional groups (A) and (B) in the molecule and a structural unit of the above (A) and (B). Examples thereof include structural units obtained (for example, structural units that can be synthesized by a technique such as allowing acrylic acid chloride to act on a hydroxyl group).

  In the structural unit (C), the crosslinkable functional group is preferably a photopolymerizable group. Examples of the photopolymerizable group include (meth) acryloyl group, alkenyl group, cinnamoyl group, cinnamylideneacetyl group, benzalacetophenone group, styrylpyridine group, α-phenylmaleimide group, phenylazide group, sulfonylazide group, Carbonyl azide group, diazo group, o-quinonediazide group, furylacryloyl group, coumarin group, pyrone group, anthracene group, benzophenone group, stilbene group, dithiocarbamate group, xanthate group, 1,2,3-thiadiazole group, cyclopropene group And azadioxabicyclo group. These may be not only one type but also two or more types. Of these, a (meth) acryloyl group and a cinnamoyl group are preferable, and a (meth) acryloyl group is particularly preferable.

Specific methods for preparing the photopolymerizable group-containing copolymer include, but are not limited to, the following methods.
a. A method of esterifying by reacting a (meth) acrylic acid chloride with a crosslinkable functional group-containing copolymer containing a hydroxyl group,
b. A method of urethanization by reacting a (meth) acrylic acid ester containing an isocyanate group with a crosslinkable functional group-containing copolymer containing a hydroxyl group,
c. A method of reacting (meth) acrylic acid with a crosslinkable functional group-containing copolymer containing an epoxy group,
d. A method in which a crosslinkable functional group-containing copolymer containing a carboxyl group is reacted with a containing (meth) acrylic acid ester containing an epoxy group for esterification.

The amount of the photopolymerizable group introduced can be arbitrarily adjusted, and the carboxyl group, hydroxyl group, etc. can be controlled from the viewpoints of surface stability of the coating film, reduction of surface failure when coexisting with inorganic particles, and improvement of film strength. You may leave.
In the present invention, the introduction amount of the structural unit for imparting crosslinkability in the copolymer is preferably 10 to 50 mol%, more preferably 15 to 45 mol%, particularly preferably 20 to 40 mol%. This is the case of mol%.

  In the copolymer useful for the low refractive index layer in the present invention, in addition to the repeating unit derived from the fluorine-containing vinyl monomer and the structural unit for imparting crosslinkability, adhesion to a substrate, polymer Tg (film) Other vinyl monomers can be appropriately copolymerized from various viewpoints such as solubility in solvents, transparency, slipperiness, dustproof / antifouling properties, etc. A plurality of these vinyl monomers may be combined depending on the purpose, and are preferably introduced in the range of 0 to 65 mol% in the copolymer in total, and in the range of 0 to 40 mol%. Is more preferable, and the range of 0 to 30 mol% is particularly preferable.

  The vinyl monomer unit that can be used in combination is not particularly limited. For example, olefins (ethylene, propylene, isoprene, vinyl chloride, vinylidene chloride, etc.), acrylic esters (methyl acrylate, methyl acrylate, ethyl acrylate, acrylic) 2-ethylhexyl acid, 2-hydroxyethyl acrylate), methacrylic acid esters (methyl methacrylate, ethyl methacrylate, butyl methacrylate, 2-hydroxyethyl methacrylate, etc.), styrene derivatives (styrene, p-hydroxymethylstyrene, p-methoxystyrene, etc.), vinyl ethers (methyl vinyl ether, ethyl vinyl ether, cyclohexyl vinyl ether, hydroxyethyl vinyl ether, hydroxybutyl vinyl ether, etc.), vinyl esters (vinyl acetate) , Vinyl propionate, vinyl cinnamate, etc.), unsaturated carboxylic acids (acrylic acid, methacrylic acid, crotonic acid, maleic acid, itaconic acid, etc.), acrylamides (N, N-dimethylacrylamide, Nt-butylacrylamide, N-cyclohexylacrylamide, etc.), methacrylamides (N, N-dimethylmethacrylamide), acrylonitrile and the like.

  The fluorine-containing copolymer particularly useful in the present invention is a random copolymer of a perfluoroolefin and vinyl ethers or vinyl esters. In particular, it preferably has a group capable of undergoing crosslinking reaction alone {a radical reactive group such as a (meth) acryloyl group, a ring-opening polymerizable group such as an epoxy group or an oxetanyl group}. These cross-linking reactive group-containing polymer units preferably occupy 5 to 70 mol%, particularly preferably 30 to 60 mol%, of the total polymerized units of the polymer. Regarding preferred polymers, JP-A-2002-243907, JP-A-2002-372601, JP-A-2003-26732, JP-A-2003-222702, JP-A-2003-294911, JP-A-2003-329804, JP-A-2004. -4444 and JP-A-2004-45462.

  In addition, the fluorine-containing copolymer useful in the present invention preferably has a polysiloxane structure introduced for the purpose of imparting antifouling properties. The method for introducing the polysiloxane structure is not limited. For example, as described in JP-A-6-93100, JP-A-11-189621, JP-A-11-228631, and JP-A-2000-313709, silicone macroazo A method for introducing a polysiloxane block copolymer component using an initiator; a method for introducing a polysiloxane graft copolymer component using a silicone macromer as described in JP-A-2-251555 and JP-A-2-308806. Is preferred. Particularly preferred compounds include the polymers of Examples 1, 2, and 3 of JP-A-11-189621, and copolymers A-2 and A-3 of JP-A-2-251555. It is preferable that these polysiloxane components are 0.5-10 mass% in a polymer, Most preferably, it is 1-5 mass%.

  The preferred molecular weight of the copolymer that can be preferably used in the present invention is a mass average molecular weight of 5000 or more, preferably 10,000 to 500,000, and most preferably 15,000 to 200,000. By using polymers having different average molecular weights in combination, it is possible to improve the surface state of the coating film and the scratch resistance.

  As described in JP-A-10-25388 and JP-A-2000-17028, a curing agent having a polymerizable unsaturated group may be appropriately used in combination with the above copolymer. Further, as described in JP-A-2002-145952, combined use with a compound having a fluorine-containing polyfunctional polymerizable unsaturated group is also preferable. Examples of the compound having a polyfunctional polymerizable unsaturated group include the polyfunctional monomer described in the antiglare layer. 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 copolymer body.

  The refractive index of the low refractive index layer is preferably 1.20 to 1.46, more preferably 1.25 to 1.42, and particularly preferably 1.30 to 1.38. The thickness of the low refractive index layer is preferably 50 to 150 nm, and more preferably 70 to 120 nm.

(Fine particles)
Next, the fine particles that can be preferably used in the low refractive index layer in the present invention will be described.

The coated amount of the fine particles contained in the low refractive index layer is preferably from 1 to 100 mg / m ^2, more preferably 1 to 80 mg / m ^2, more preferably from 1~70mg / m ^2. If the coating amount of the fine particles is greater than or equal to the lower limit value, the effect of improving the scratch resistance is clearly manifested. If the coating amount is smaller than or equal to the upper limit value, fine irregularities are formed on the surface of the low refractive index layer, and the appearance and integrated reflectance This is preferable because there is no problem such as deterioration. Since the fine particles are contained in the low refractive index layer, the low refractive index is preferable.

Specifically, the fine particles contained in the low refractive index layer are inorganic fine particles, hollow inorganic fine particles, or hollow organic resin fine particles, preferably having a low refractive index, particularly hollow inorganic fine particles. preferable. Examples of the inorganic fine particles include silica or hollow silica fine particles. The average particle size of such fine particles is preferably 30% or more and 100% or less of the thickness of the low refractive index layer, more preferably 30% or more and 80% or less, and further preferably 35% or more and 70% or less. That is, when the thickness of the low refractive index layer is 100 nm, the particle size of the fine particles is preferably 30 nm to 100 nm, more preferably 30 nm to 80 nm, and still more preferably 35 nm to 70 nm.
In order to enhance the scratch resistance, it is preferable that inorganic layers are contained in the entire antiglare film, and most preferably, silica particles are contained in the entire antiglare film. .

  The (hollow) silica fine particles as described above clearly show the effect of improving the scratch resistance when the particle diameter is not less than the above lower limit value. This is preferable because irregularities are formed and problems such as deterioration in appearance and integrated reflectance do not occur.

  The (hollow) silica fine particles may be either crystalline or amorphous, and may be monodisperse particles, aggregated particles (in this case, the secondary particle diameter is 30% to 100% of the layer thickness of the low refractive index layer) It may be preferable). Two or more types of particles (types or particle sizes) may be used. The particle shape is most preferably a spherical diameter, but there is no problem even if it is indefinite.

In order to lower the refractive index of the low refractive index layer, it is particularly preferable to use hollow silica fine particles. The hollow silica fine particles have a refractive index of 1.17 to 1.40, more preferably 1.17 to 1.35, and still more preferably 1.17 to 1.30. The refractive index here represents the refractive index of the entire particle, and does not represent the refractive index of only the outer shell silica forming the hollow silica particles. At this time, the radius r _i of the cavity inside the particle, the radius of the outer shell of the particle is r _o, the porosity x is calculated by the following equation (1).

Equation (1): x = (4πr i 3/3) / (4πr o 3/3) × 100

  The porosity x is preferably 10 to 60%, more preferably 20 to 60%, and most preferably 30 to 60%. If the hollow silica particles are made to have a lower refractive index and a higher porosity, the thickness of the outer shell becomes thinner and the strength of the particles becomes weaker. From the viewpoint of scratch resistance, the low refractive index is less than 1.17. Rate particles are difficult. In addition, the refractive index of these hollow silica particles was measured with an Abbe refractometer {manufactured by Atago Co., Ltd.}.

  In the present invention, it is preferable to further reduce the surface free energy of the surface of the low refractive index layer from the viewpoint of improving the antifouling property. Specifically, it is preferable to use a fluorine-containing compound or a compound having a polysiloxane structure for the low refractive index layer.

  Examples of the additive having a polysiloxane structure include a reactive group-containing polysiloxane {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. These polysiloxanes are preferably added in the range of 0.1 to 10% by mass of the total solid content of the low refractive index layer, particularly preferably 1 to 5% by mass.

[Other components contained in the composition for forming an antiglare layer and / or a low refractive index layer]
[Organosilane compound]
At least one of the layers constituting the antiglare film of the present invention is at least one component of a hydrolyzate of an organosilane compound and / or a partial condensate thereof, a so-called sol component (hereinafter referred to as such). From the viewpoint of scratch resistance. In particular, in an antiglare film having a low refractive index layer, it is particularly preferable to contain a sol component in the low refractive index layer in order to achieve both antireflection performance and scratch resistance. This sol component is condensed by a drying and heating process after coating to form a cured product, and becomes a part of the binder of the low refractive index layer. Moreover, when this hardened | cured material has a polymerizable unsaturated bond, the binder which has a three-dimensional structure is formed by irradiation of actinic light.

The organosilane compound is preferably represented by the following general formula (1).
Formula _{^{(1) :( R 11) m1}} -Si (X 11) 4-m1

In the general formula (1), R ¹¹ represents a substituted or unsubstituted alkyl group or a substituted or unsubstituted aryl group. As an alkyl group, a C1-C30 alkyl group is preferable, More preferably, it is C1-C16, Most preferably, it is a C1-C6 thing. Specific examples of the alkyl group include methyl, ethyl, propyl, isopropyl, hexyl, decyl, hexadecyl and the like. Examples of the aryl group include phenyl and naphthyl, and a phenyl group is preferable.

X ¹¹ represents a hydroxyl group or a hydrolyzable group, for example, an alkoxy group (preferably an alkoxy group having 1 to 5 carbon atoms, such as a methoxy group or an ethoxy group), a halogen atom (for example, Cl, Br, I And a group represented by R ¹² COO (R ¹² is preferably a hydrogen atom or an alkyl group having 1 to 6 carbon atoms, such as CH ₃ COO, C ₂ H ₅ COO, etc.), preferably Is an alkoxy group, particularly preferably a methoxy group or an ethoxy group. m1 represents the integer of 1-3, Preferably it is 1-2.

When X ¹¹ there are a plurality, it may be different even multiple X ¹¹ is the same, respectively. The substituent contained in R ¹¹ is not particularly limited, but a halogen atom (fluorine, chlorine, bromine, etc.), hydroxyl group, mercapto group, carboxyl group, epoxy group, alkyl group (methyl, ethyl, i-propyl, propyl, t-butyl etc.), aryl groups (phenyl, naphthyl etc.), aromatic heterocyclic groups (furyl, pyrazolyl, pyridyl etc.), alkoxy groups (methoxy, ethoxy, i-propoxy, hexyloxy etc.), aryloxy (phenoxy etc.) ), Alkylthio groups (methylthio, ethylthio, etc.), arylthio groups (phenylthio, etc.), alkenyl groups (vinyl, 1-propenyl, etc.), acyloxy groups (acetoxy, acryloyloxy, methacryloyloxy, etc.), alkoxycarbonyl groups (methoxycarbonyl, ethoxy) Carbonyl, etc.), aryloxy Carbonyl groups (such as phenoxycarbonyl), carbamoyl groups (such as carbamoyl, N-methylcarbamoyl, N, N-dimethylcarbamoyl, N-methyl-N-octylcarbamoyl), acylamino groups (acetylamino, benzoylamino, acrylicamino, methacrylamino) Etc.), and these substituents may be further substituted. R ¹¹ is preferably a substituted alkyl group or a substituted aryl group.

  Moreover, the organosilane compound which has a vinyl polymerizable substituent represented by following General formula (2) is also preferable.

In the general formula (2), R ²¹ represents a hydrogen atom, a methyl group, a methoxy group, an alkoxycarbonyl group, a cyano group, a fluorine atom, or a chlorine atom. Examples of the alkoxycarbonyl group include a methoxycarbonyl group and an ethoxycarbonyl group. A hydrogen atom, a methyl group, a methoxy group, a methoxycarbonyl group, a cyano group, a fluorine atom, and a chlorine atom are preferable, a hydrogen atom, a methyl group, a methoxycarbonyl group, a fluorine atom, and a chlorine atom are more preferable, and a hydrogen atom and a methyl group Is particularly preferred.

Y ²¹ represents a single bond or * -COO-**, * -CONH-** or * -O-**, preferably a single bond, * -COO-** or * -CONH-**. Bonds and * -COO-** are more preferred, and * -COO-** is particularly preferred. * Represents a position bonded to ═C (R ²¹ ) —, and ** represents a position bonded to L ²¹ .

L ²¹ represents a divalent linking chain. Specifically, a substituted or unsubstituted alkylene group, a substituted or unsubstituted arylene group, a substituted or unsubstituted alkylene group having a linking group (for example, ether, ester, amide, etc.) inside, and a linking group inside. A substituted or unsubstituted arylene group, a substituted or unsubstituted alkylene group, a substituted or unsubstituted arylene group, an alkylene group having a linking group therein is preferred, an unsubstituted alkylene group, an unsubstituted arylene group Further, an alkylene group having an ether or ester linking group inside is more preferred, an unsubstituted alkylene group, and an alkylene group having an ether or ester linking group inside is particularly preferred. Examples of the substituent include a halogen, a hydroxyl group, a mercapto group, a carboxyl group, an epoxy group, an alkyl group, and an aryl group, and these substituents may be further substituted.

  a1 (represents a number satisfying the mathematical formula of a1 = 100−a2) and a2 represent a molar ratio, and a2 represents a number of 0 to 50. As for a2, the number of 0-40 is more preferable, and the number of 0-30 is especially preferable.

R ^{22 to} R ²⁵ are preferably a halogen atom, a hydroxyl group, an unsubstituted alkoxy group, or an unsubstituted alkyl group. R ^{22 to} R ²⁴ are more preferably a chlorine atom, a hydroxyl group, or an unsubstituted alkoxy group having 1 to 6 carbon atoms, more preferably a hydroxyl group or an alkoxy group having 1 to 3 carbon atoms, and particularly preferably a hydroxyl group or a methoxy group. R ²⁵ represents a hydrogen atom, an alkyl group, an alkoxy group, an alkoxycarbonyl group, a cyano group, a fluorine atom, or a chlorine atom. Examples of the alkyl group include a methyl group and an ethyl group. Examples of the alkoxy group include a methoxy group, an ethoxy group, and an alkoxycarbonyl group as a methoxycarbonyl group and an ethoxycarbonyl group. A hydrogen atom, a methyl group, a methoxy group, a methoxycarbonyl group, a cyano group, a fluorine atom, and a chlorine atom are preferable, a hydrogen atom, a methyl group, a methoxycarbonyl group, a fluorine atom, and a chlorine atom are more preferable, and a hydrogen atom and a methyl group Is particularly preferred. R ²⁶ has the same meaning as R ^{11 in} the general formula (1), more preferably a hydroxyl group or an unsubstituted alkyl group, still more preferably a hydroxyl group or an alkyl group having 1 to 3 carbon atoms, and particularly preferably a hydroxyl group or a methyl group. preferable.

  Two or more compounds of the general formula (1) may be used in combination. The compound of the general formula (2) is synthesized using at least one kind of the compound of the general formula (1) as a starting material. Specific examples of the compound of the general formula (1) include, but are not limited to, the compounds described in [0073] to [0079] of JP-A No. 2007-164166.

  Of these, (M-1), (M-2), and (M-25) are particularly preferable as the organosilane containing a polymerizable group.

  In order to obtain the effects of the present invention, the content of the organosilane containing the vinyl polymerizable group in the hydrolyzate of organosilane and / or its partial condensate is preferably 30% by mass to 100% by mass, and 50 The mass% is more preferably 100% by mass, and more preferably 70% by mass to 95% by mass. If the content of the organosilane containing the vinyl polymerizable group is 30% by mass or more, a solid matter may be formed in the coating solution for forming the antiglare layer and / or the low refractive index layer, the solution may become cloudy, There are no inconveniences such as deterioration of life and difficulty in controlling molecular weight (increase in molecular weight), and performance when polymerizing treatment is performed due to low content of polymerizable groups (for example, antireflection film This is preferable because problems such as difficulty in improving scratch resistance do not occur.

  When synthesizing the compound represented by the general formula (2), (M-1) described in [0073] to [0079] of JP-A No. 2007-164166 as an organosilane containing the vinyl polymerizable group. , (M-2), (M-19) to (M-21) and (M-48) are used as organosilanes having no vinyl polymerizable group, respectively, in combination with the above amounts. And preferred.

[Polymerization initiator]
(Photopolymerization initiator)
Examples of photo radical polymerization initiators include acetophenones, benzoins, benzophenones, phosphine oxides, ketals, anthraquinones, thioxanthones, azo compounds, peroxides (JP-A-2001-139663, etc.), 2, Examples include 3-dialkyldione compounds, disulfide compounds, fluoroamine compounds, aromatic sulfoniums, lophine dimers, onium salts, borates, active esters, active halogens, inorganic complexes, and coumarins.

As a commercially available photo radical polymerization initiator, “Kayacure (DETX-S, BP-100, BDDK, CTX, BMS, 2-EAQ, ABQ, CPTX, EPD, ITX, QTX, BTC” manufactured by Nippon Kayaku Co., Ltd. , MCA, etc.) ”,“ Irgacure (651, 184, 500, 819, 907, 127, 369, 1173, 1870, 2959, 4265, 4263, etc.) ”manufactured by Ciba Specialty Chemicals, Inc., manufactured by Sartomer Preferred examples include "Esacure (KIP100F, KB1, EB3, BP, X33, KT046, KT37, KIP150, TZT)" and the like.

  It is preferable to use a photoinitiator in the range of 0.1-15 mass parts with respect to 100 mass parts of polyfunctional monomers, More preferably, it is the range of 1-10 mass parts.

(Photosensitizer)
In addition to the photopolymerization initiator, a photosensitizer may be used. Specific examples of the photosensitizer include n-butylamine, triethylamine, tri-n-butylphosphine, Michler's ketone and thioxanthone.
Further, one or more auxiliary agents such as an azide compound, a thiourea compound, and a mercapto compound may be used in combination.

  Examples of commercially available photosensitizers include “Kaya Cure (DMBI, EPA)” manufactured by Nippon Kayaku Co., Ltd.

(Thermal initiator)
As the thermal radical initiator, organic or inorganic peroxides, organic azo, diazo compounds, and the like can be used. Specifically, benzoyl peroxide, halogen benzoyl peroxide, lauroyl peroxide, acetyl peroxide, dibutyl peroxide, cumene hydroperoxide, butyl hydroperoxide as organic peroxides, hydrogen peroxide, peroxides as inorganic peroxides. Diazo compounds such as 2,2′-azobis (isobutyronitrile), 2,2′-azobis (propionitrile), 1,1′-azobis (cyclohexanecarbonitrile) as azo compounds such as ammonium sulfate and potassium persulfate And diazoaminobenzene, p-nitrobenzenediazonium and the like.

[Crosslinking agent (crosslinkable compound)]
When the monomer or polymer binder constituting the antiglare layer and the low refractive index layer of the present invention alone does not have sufficient curability, the necessary curability can be imparted by blending a crosslinkable compound. it can. In particular, it is effective to contain it in the low refractive index layer. 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.

  Melamine compounds are generally known as compounds having a skeleton in which a nitrogen atom is bonded to a triazine ring, and specific examples include melamine, alkylated melamine, methylol melamine, alkoxylated methyl melamine, and the like. However, it is preferable to have one or both of a methylol group and an alkoxylated methyl group in one molecule in total.

  Specifically, methylolated melamine, alkoxylated methylmelamine, or a derivative thereof obtained by reacting melamine and formaldehyde under basic conditions is preferable, and good storage stability is obtained particularly for the curable resin composition. Alkoxylated methyl melamine is preferable in that it can be obtained and good reactivity can be obtained. There are no particular restrictions on the methylolated melamine and the alkoxylated methylmelamine used as the crosslinkable compound. Various resinous materials can be used.

  In addition to urea, examples of the urea compound include polymethylolated urea, alkoxylated methylurea which is a derivative thereof, methylolated uron having a uron ring, and alkoxylated methyluron. And also about compounds, such as a urea derivative, the use of the various resinous materials described in said literature is possible.

(Curing catalyst)
In the film of the present invention, a curing catalyst that generates radicals and acids upon irradiation with ionizing radiation or heat can be used as a curing catalyst for promoting curing.

(Thermal acid generator)
As an example of the antiglare film of the present invention, by heating, the film can be cured by a crosslinking reaction between a hydroxyl group of the fluorinated copolymer and a curing agent capable of crosslinking with the hydroxyl group. In this system, since the curing is accelerated by acid, it is desirable to add an acidic substance to the curable resin composition. However, when a normal acid is added, the crosslinking reaction proceeds in the coating solution, and failure (unevenness, Therefore, in order to achieve both storage stability and curing activity in a thermosetting system, it is more preferable to add a compound that generates an acid by heating as a curing catalyst.

  The curing catalyst is preferably a salt composed of an acid and an organic base. Examples of the acid include organic acids such as sulfonic acid, phosphonic acid, and carboxylic acid, and inorganic acids such as sulfuric acid and phosphoric acid. From the viewpoint of compatibility with the polymer, organic acids are more preferable, and sulfonic acid and phosphonic acid are more preferable. Sulphonic acid is most preferred. Preferred sulfonic acids include p-toluenesulfonic acid (PTS), benzenesulfonic acid (BS), p-dodecylbenzenesulfonic acid (DBS), p-chlorobenzenesulfonic acid (CBS), 1,4-naphthalenedisulfonic acid (NDS). ), Methanesulfonic acid (MSOH), nonafluorobutane-1-sulfonic acid (NFBS) and the like, and any of them can be preferably used (the abbreviations in parentheses).

  Commercially available materials for the thermal acid generator include “Catalyst 4040”, “Catalyst 4050”, “Catalyst 600”, “Catalyst 602”, “Catalyst 500”, “Catalyst 296-9”. {Nippon Cytec Industries, Ltd.}, “NACURE series 155, 1051, 5076, 4054J” and its block type “NACURE series 2500, 5225, X49-110, 3525, 4167” (manufactured by King) Is mentioned.

  The use ratio of the thermal acid generator is preferably 0.01 to 10 parts by mass, preferably 0.1 to 5 parts by mass, and more preferably 0.2 to 3 parts per 100 parts by mass of the curable resin composition. The mass. When the addition amount is within this range, the storage stability of the curable resin composition is good and the scratch resistance of the coating film is also good.

(Formation of a low refractive index layer)
In the antiglare film of the present invention, the low refractive index layer can be formed by coating, and an ultraviolet (UV) curing and / or heat is used as a film forming component in the coating liquid for forming the low refractive index layer. It is preferable to have at least one translucent resin having a curable functional group. {The translucent resin having a functional group capable of ultraviolet (UV) curing and / or heat curing is preferably a fluorine-containing copolymer described above. Polymer, organosilane compound, etc.}.

Further, in the antiglare film of the present invention, the coating liquid for forming the low refractive index layer contains at least two kinds of translucent resins as a film forming component, and at least one kind of translucent resin is included. It is more preferable that at least one kind of translucent resin having a functional group capable of ultraviolet (UV) curing has a functional group capable of being thermally cured. In addition, it is more preferable that the coating liquid for forming the low refractive index layer contains at least one polymerization initiator and at least one thermosetting crosslinking agent. In addition, it is even more preferable that the low refractive index layer contains a curing catalyst that promotes thermal curing (the polymerization initiator, the crosslinking agent that can be thermally cured, and the curing catalyst that promotes thermal curing are described above. Can be preferably used).

  Further, in the antiglare film of the present invention, a translucent resin having at least an ultraviolet (UV) curable functional group contained in the coating solution for forming the low refractive index layer, and at least one polymerization initiator The value obtained by dividing the sum of the total mass and the mass of the translucent resin having at least one thermosetting functional group by the total mass of the at least one thermosetting crosslinker is 0.05 to 0.00. 19 is preferable in terms of scratch resistance and cost. More preferably, it is 0.10-0.19, More preferably, it is 0.15-0.19. If this value is 0.05 or more, it is preferable because scratch resistance is good, and if it is 0.20 or less, the ratio of the UV curing component becomes appropriate, so that the polymerization efficiency during UV curing is increased. Process conditions (nitrogen purge during UV curing, film surface temperature increase, etc.) are preferable because they become appropriate.

  The oxygen concentration during UV curing by nitrogen purge is preferably 1000 ppm or less, more preferably 500 ppm or less, still more preferably 100 ppm or less, and most preferably 50 ppm or less. The film surface temperature during UV curing is preferably 50 ° C. or higher, more preferably 70 ° C. or higher, and still more preferably 90 ° C. or higher. If the temperature is equal to or lower than the upper limit value, there is no inconvenience such as softening of the support and causing a handling (conveyance) defect. Therefore, the upper limit temperature is preferably determined within this range.

[Leveling agent]
Various leveling agents are preferably used in the at least one antiglare layer of the present invention for the purpose of improving the surface condition (preventing unevenness). Furthermore, it is preferable to use various leveling agents for the purpose of preventing unevenness in the low refractive index layer of the present invention.

  Specifically, the leveling agent is preferably a fluorine-based leveling agent or a silicone-based leveling agent. In particular, it is more preferable to use both a fluorine-based leveling agent and a silicone-based leveling agent because of their high ability to prevent unevenness. Moreover, it is more preferable that a leveling agent is used for all layers. The leveling agent is preferably an oligomer or a polymer rather than a low molecular compound.

  When a leveling agent is added, the leveling agent quickly moves to the surface of the applied liquid film and becomes unevenly distributed, and even after the film is dried, the leveling agent is unevenly distributed on the surface, so the antiglare layer to which the leveling agent is added In addition, the surface energy of the film of the low refractive index layer is lowered by the leveling agent. Therefore, from the viewpoint of preventing unevenness of the antiglare layer, it is preferable that the surface energy of the antiglare layer is low.

  Below, a preferable fluorine-type leveling agent as a leveling agent of a glare-proof layer is demonstrated. The silicone leveling agent will be described later.

(Fluorine leveling agent)
As the fluorine-based leveling agent, a polymer having a fluoroaliphatic group is preferable, and a polymer of a repeating unit (polymerization unit) corresponding to the monomer (i) below, or a repeating unit corresponding to the monomer (i) below. A copolymer of an acrylic resin, a methacrylic resin, and a vinyl monomer copolymerizable therewith containing a (polymerized unit) and a repeating unit (polymerized unit) corresponding to the monomer (ii) below is useful. Such monomers include "Polymer Handbook 2nd ed." Brandrup, Wiley lnterscience (1975), Chapter 2, P.I. 1-483 can be used, for example, addition selected from acrylic acid, methacrylic acid, acrylic esters, methacrylic esters, acrylamides, methacrylamides, allyl compounds, vinyl ethers, vinyl esters, etc. Examples thereof include a compound having one polymerizable unsaturated bond.

  (I) Fluoroaliphatic group-containing monomer represented by the following general formula (4-1)

In the above general formula (4-1), R ⁴¹ represents a hydrogen atom, a halogen atom or a methyl group, preferably a hydrogen atom or a methyl group. Y ⁴¹ represents an oxygen atom, a sulfur atom or —N (R ⁴² ) —, more preferably an oxygen atom or —N (R ⁴² ) —, and still more preferably an oxygen atom. R ⁴² represents an alkyl group having 1 to 8 carbon hydrogen atom or a carbon atoms which may have a substituent, more preferably a hydrogen atom or an alkyl group having 1 to 4 carbon atoms, more preferably a hydrogen atom or a methyl group. Rf ⁴¹ represents -CF ₃ or -CF ₂ H.

M in the general formula (4-1) represents an integer of 1 to 6, more preferably 1 to 3, and still more preferably 1. n represents an integer of 1 to 11, more preferably 1 to 9, and still more preferably 1 to 6. Rf ⁴¹ is preferably —CF ₂ H.

  Further, in the (co) polymer having a fluoroaliphatic group, two or more kinds of polymer units derived from the fluoroaliphatic group-containing monomer represented by the general formula (4-1) are contained as constituent components. Also good.

  (Ii) Monomer represented by the following general formula (4-2) copolymerizable with the above (i)

In the above general formula (4-2), R ⁴³ represents a hydrogen atom, a halogen atom or a methyl group, and more preferably a hydrogen atom or a methyl group. Y ⁴² represents an oxygen atom, a sulfur atom or -N (R ⁴⁵⁾ - represents a oxygen atom or -N (R ⁴⁵⁾ - is more preferably an oxygen atom. R ⁴⁵ represents a hydrogen atom or an alkyl group having 1 to 8 carbon atoms, more preferably a hydrogen atom or an alkyl group having 1 to 4 carbon atoms, and still more preferably a hydrogen atom or a methyl group. R ⁴⁴ is a linear, branched or cyclic alkyl group having 1 to 60 carbon atoms which may have a substituent, or an aromatic group which may have a substituent (for example, phenyl group or naphthyl). Group). The alkyl group may include a poly (alkyleneoxy) group. Furthermore, a linear, branched or cyclic alkyl group having 1 to 20 carbon atoms is more preferable, and a linear or branched alkyl group having 1 to 10 carbon atoms is very preferable. The amount of the fluoroaliphatic group-containing monomer represented by the general formula (4-1) used for the production of a preferred (co) polymer having a fluoroaliphatic group is based on the total amount of the monomer of the copolymer. It is 10 mass% or more, Preferably it is 50 mass% or more, More preferably, it is 70-100 mass%, More preferably, it is the range of 80-100 mass%.

  Hereinafter, specific examples of the structure of a preferred (co) polymer having a fluoroaliphatic group include those described in JP 2007-72100 A [0158] to [0160], but are not limited thereto.

  The amount of polymer units of the fluoroaliphatic group-containing monomer constituting the (co) polymer having a fluoroaliphatic group is preferably more than 10% by mass, more preferably 50 to 100% by mass, and antiglare From the viewpoint of preventing unevenness of the layer, it is most preferably 75 to 100% by mass, and when a low refractive index layer is applied on the antiglare layer, it is 50 to 75% by mass. Most preferred. (Described in all polymer units constituting a (co) polymer having a fluoroaliphatic group)

(Silicone leveling agent)
Next, the silicone leveling agent will be described.
Preferable examples of the silicone compound include those having a substituent at the end of the compound chain and / or the side chain, containing a plurality of dimethylsilyloxy units as repeating units. The compound chain containing dimethylsilyloxy as a repeating unit may contain a structural unit other than dimethylsilyloxy. The substituents may be the same or different, and a plurality of substituents are preferable. Examples of preferred substituents include polyether groups, alkyl groups, aryl groups, aryloxy groups, acryloyl groups, methacryloyl groups, vinyl groups, aryl groups, cinnamoyl groups, epoxy groups, oxetanyl groups, hydroxyl groups, fluoroalkyl groups, polyoxy groups. Examples thereof include an alkylene group, a carboxyl group, an amino group and the like.

  Although there is no restriction | limiting in particular in molecular weight, It is preferable that it is 100,000 or less, It is more preferable that it is 50,000 or less, It is especially preferable that it is 1000-30000, It is most preferable that it is 1000-20000.

  Although there is no restriction | limiting in particular in silicone atom content of a silicone type compound, it is preferable that it is 18.0 mass% or more, it is especially preferable that it is 25.0-37.8 mass%, and 30.0-37.0. Most preferably, it is mass%.

  Examples of preferable silicone compounds include “X-22-174DX”, “X-22-2426”, “X-22-164B”, “X22-164C”, “X-” manufactured by Shin-Etsu Chemical Co., Ltd. 22-170DX "," X-22-176D "," X-22-1821 "(named above);" FM-0725 "," FM-7725 "," FM-4421 "manufactured by Chisso Corporation, “FM-5521”, “FM-6621”, “FM-1121” (named above); “DMS-U22”, “RMS-033”, “RMS-083”, “UMS-182” manufactured by Gelest, “DMS-H21”, “DMS-H31”, “HMS-301”, “FMS121”, “FMS123”, “FMS131”, “FMS141”, “FMS221” (named above); Toray Dow “SH200”, “DC11PA”, “SH28PA”, “ST80PA”, “ST86PA”, “ST97PA”, “SH550”, “SH710”, “L7604”, “FZ-2105”, “FZ2123” manufactured by Corning Co., Ltd. ”,“ FZ2162 ”,“ FZ-2191 ”,“ FZ2203 ”,“ FZ-2207 ”,“ FZ-3704 ”,“ FZ-3736 ”,“ FZ-3501 ”,“ FZ-3789 ”,“ L-77 ” ”,“ L-720 ”,“ L-7001 ”,“ L-7002 ”,“ L-7604 ”,“ Y-7006 ”,“ SS-2801 ”,“ SS-2802 ”,“ SS-2803 ”, "SS-2804", "SS-2805" (named above); "TSF400", "TSF401", "TSF410" manufactured by GE Toshiba Silicone Co., Ltd. TSF433 "," TSF4450 "," TSF4460 "(trade name); is are exemplified but not limited thereto such.

  The amount of the fluorine-containing leveling agent and silicone leveling agent added to the coating solution is preferably 0.001 to 1.0% by mass, more preferably 0.01% to 0.2% by mass. .

[Liquid solvent for low refractive index layer]
The coating liquid solvent of the low refractive index layer of the antiglare film of the present invention is a low boiling point solvent having a boiling point of 120 ° C. or lower, in order to suppress drying unevenness of the low refractive index layer, and the total mass of the coating liquid solvent of the low refractive index layer. 50 to 100% by mass, preferably 70 to 100% by mass, and more preferably 90 to 100% by mass. By changing the solvent composition of the low refractive index layer of the sample of the present invention described later as described above, this effect could be confirmed in the surface evaluation of the low refractive index layer. Specific examples of the coating solution solvent include methyl ethyl ketone, methyl isobutyl ketone, and toluene, which have good solubility of the fluorine-containing polymer in the low refractive index layer.

[Thickener for anti-glare layer]
In the antiglare layer, a thickener may be used to adjust the viscosity of the coating solution.
By increasing the viscosity, the sedimentation of contained particles can be suppressed, and the effect of preventing unevenness can be expected. The term “thickener” as used herein means that the viscosity of the liquid is increased by adding it, and is preferably 0.05 to 50 cP as the magnitude of increase in the viscosity of the coating liquid by adding it. More preferably, it is 1-50 cP, Most preferably, it is 2-50 cP.

  It is preferable that the polymer used as the thickener does not substantially contain a fluorine atom and / or a silicon atom. Here, “substantially” means that the content of fluorine atoms and / or silicon atoms in the mass of the polymer is 0.1% by mass or less, preferably 0.01% by mass or less.

Such a thickener is preferably a high molecular polymer, and specific examples include, but are not limited to, the following.
High molecular weight polymer thickener:
Polyacrylate,
Polymethacrylate,
Polyvinyl acetate,
Vinyl propionate,
Polyvinyl butyrate,
Polyvinyl butyral,
Polyvinyl formal,
Polyvinyl acetal,
Polyvinylpropanal,
Polyvinyl hexanal,
Polyvinylpyrrolidone,
Cellulose acetate,
Cellulose propionate,
Cellulose acetate butyrate.

Of these, polymethacrylates (specifically, polymethyl methacrylate and polyethyl methacrylate), polyvinyl acetate, vinyl polypropionate, cellulose propionate, and cellulose acetate butyrate are particularly preferable.
Further, those having a mass average molecular weight of 100,000 to 1,000,000 are preferable.

  In addition, smectite, tetrasilica mica, bentonite, silica, montmorillonite and sodium polyacrylate described in JP-A-8-325491, ethylcellulose, polyacrylic acid, organic clay described in JP-A-10-219136, etc. Well-known viscosity modifiers and thixotropic agents can be used.

(Transparent support)
As the transparent support of the antiglare film of the present invention, it is preferable to use a plastic film. Examples of the polymer forming the plastic film include cellulose esters {for example, triacetyl cellulose, diacetyl cellulose, typically “TAC-TD80U”, “TD80UF”, etc., manufactured by Fuji Film Co., Ltd.)}, polyamide, polycarbonate, polyester (for example, , Polyethylene terephthalate, polyethylene naphthalate), polystyrene, polyolefin, norbornene resin {"Arton" (trade name), manufactured by JSR Corporation}, amorphous polyolefin {"ZEONEX" (trade name), ZEON CORPORATION Etc.}. Of these, triacetyl cellulose, polyethylene terephthalate, and polyethylene naphthalate are preferable, and triacetyl cellulose is particularly preferable. In addition, a cellulose acylate film substantially free of halogenated hydrocarbons such as dichloromethane and a method for producing the same are disclosed in JIII Journal of Technical Disclosure (Publication No. 2001-1745, published on March 15, 2001; (Abbreviated as No. 2001-1745), and the cellulose acylate described therein can also be preferably used in the present invention.

  The thickness of the transparent support is preferably from 20 to 200 μm, preferably from 30 to 100 μm, more preferably from 35 to 90 μm, most preferably from 40 to 40 μm, considering the need for thinning and handling (conveyability). 80 μm.

  The width of the transparent support can be arbitrarily selected, but usually 100 to 5000 mm is used from the viewpoint of increasing the size of the image display device, handling (conveyability), yield, and productivity. It is preferable that it is 800-3000 mm, and it is more preferable that it is 1000-2000 mm.

[Characteristics of antiglare film]
The total light transmittance of the antiglare film of the present invention is measured according to JIS K-7316. The total light transmittance is preferably 85% or more from the viewpoint of front contrast. More preferably, it is 90% or more, and particularly preferably 92% or more.

  The contact angle of the antiglare film surface of the present invention with respect to pure water measured in an environment of 25 ° C. and 60% RH is preferably 90 ° or more from the viewpoint of antifouling properties. More preferably, it is 95 ° or more, and particularly preferably 100 ° or more. Further, the change in the contact angle before and after the saponification treatment (described later) required for polarizing plate processing is preferably 5 ° or less, more preferably 3 ° or less, and most preferably 1 ° or less.

[Antistatic layer]
The antiglare film of the present invention may be provided with an antistatic layer containing various conductive particles in order to impart conductivity.

  The dynamic friction coefficient of the antiglare film surface of the present invention is preferably 0.3 or less from the viewpoint of improving the scratch resistance (preventing stress concentration). More preferably, it is 0.2 or less, more preferably 0.1 or less.

  In the antiglare film of the present invention, when the average value of 5 ° regular reflectance in the wavelength region of 450 nm to 650 nm is A and the average value of integrated reflectance is B, B is 3% or less, B -A is preferably 1.5% or less from the viewpoint of tightening black display in a bright room environment and improving bright room contrast. B is more preferably 2% or less, and further preferably 1% or less. Further, B-A is more preferably 1% or less, and further preferably 0.5% or less.

Measurement of the average value of the 5 ° regular reflectance and the integral reflectance is as follows.
The specular reflectivity is measured by attaching an adapter “ARV-474” to a spectrophotometer “V-550” [manufactured by JASCO Corporation], and an emission angle at an incident angle of 5 ° in a wavelength region of 380 to 780 nm. The specular reflectance at −5 ° was measured, and the average specular reflectance at 450 to 650 nm was calculated. The integral reflectance is measured by attaching an adapter “ILV-471” to a spectrophotometer “V-550” [manufactured by JASCO Corporation] and integrating reflection at an incident angle of 5 ° in a wavelength range of 380 to 780 nm. The rate was measured, and the average integrated reflectance of 450 to 650 nm was calculated.

The surface strength of the antiglare film is preferably H or more, more preferably 2H or more, and most preferably 3H or more in a pencil hardness test.
Furthermore, in the Taber test according to JIS K-5400, the smaller the wear amount of the test piece before and after the test, the better.

[Preparation method of antiglare film]
The antiglare film of the present invention can be formed by the following method, but is not limited thereto.

[filtration]
The coating solution used for coating is preferably filtered before coating. As the filter for filtration, it is preferable to use a filter having a pore diameter as small as possible within the range in which the components in the coating solution are not removed. For filtration, a filter having an absolute filtration accuracy of 0.1 to 50 μm, and an absolute filtration accuracy of 0.1 to 40 μm is preferably used. The thickness of the filter is preferably 0.1 to 10 mm, and more preferably 0.2 to 2 mm. In that case, the filtration pressure is preferably 1.5 MPa or less, more preferably 1.0 MPa or less, and further preferably 0.2 MPa or less.

[Processing before coating]
The transparent support used in the present invention is preferably subjected to a heat treatment for correcting base deformation, or a surface treatment for improving coating properties and adhesion with a coating layer before coating. Specific methods for the surface treatment include corona discharge treatment, glow discharge treatment, flame treatment, acid treatment, alkali treatment, and ultraviolet irradiation treatment. In addition, as described in JP-A-7-333433, it is preferable to provide an undercoat layer.

[Application]
Each layer of the 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 and extrusion coating method (die coating method) (US Pat. No. 2,681,294, International Publication No. 2005/123274) A known method such as a microgravure coating method is used, and among these, a microgravure coating method and a die coating method are preferable.

  In order to supply the film of the present invention with high productivity, an extrusion method (die coating method) is preferably used. In particular, the extrusion method described in JP-A-2006-122889 can be applied particularly preferably.

  Since the die coating method is a pre-measuring method, it is easy to ensure a stable film thickness. This coating method can be applied at high speed and with good film thickness stability to a coating solution of a low coating amount. Although application is possible by other application methods, the dip coating method inevitably causes vibration of the application liquid in the liquid receiving tank, and stepped unevenness is likely to occur. In the reverse roll coating method, stepped unevenness is liable to occur due to roll eccentricity and deflection related to coating. Further, since these coating methods are post-measuring methods, it is not easy to ensure a stable film thickness. It is preferable from the viewpoint of productivity that the die coating method is applied at a rate of 25 m / min or more.

[Dry]
The film of the present invention is preferably applied on a transparent support directly or via another layer, and then conveyed by a web to a heated zone to dry the solvent.
Various knowledges can be used as a method for drying the solvent. Specific knowledge includes description techniques such as JP 2001-286817 A, 2001-314798, 2003-126768, 2003-315505, and 2004-34002.

[Curing]
The antiglare film of the present invention can be cured after passing through a zone in which each coating film is cured by ionizing radiation and / or heat as a web after drying of the solvent. The ionizing radiation species in the present invention are preferably ultraviolet rays and electron beams, and ultraviolet rays are particularly preferred because they are easy to handle and high energy can be easily obtained.

  As the ultraviolet light source for photopolymerizing the ultraviolet curable compound, any light source that generates ultraviolet light can be used. For example, a low pressure mercury lamp, a medium pressure mercury lamp, a high pressure mercury lamp, an ultrahigh pressure mercury lamp, a carbon arc lamp, a metal halide lamp, a xenon lamp, or the like can be used. An ArF excimer laser, a KrF excimer laser, an excimer lamp, synchrotron radiation, or the like can also be used. Among these, an ultrahigh pressure mercury lamp, a high pressure mercury lamp, a low pressure mercury lamp, a carbon arc, a xenon arc, and a metal halide lamp can be preferably used.

The irradiation conditions vary depending on individual lamps, but the amount of light irradiated is preferably 10 mJ / cm ² or more, more preferably, a 50~10000mJ / cm ^2, particularly preferably 50~2000mJ / cm ^2. At that time, the irradiation distribution in the width direction of the web is preferably 50 to 100%, more preferably 80 to 100%, including both ends with respect to the central maximum irradiation.

  In the present invention, at least one layer laminated on the transparent support is irradiated with ionizing radiation and heated to a film surface temperature of 50 ° C. or more for 0.5 seconds or more from the start of ionizing radiation irradiation, and an oxygen concentration of 1000 ppm. Preferably, it is cured by a step of irradiating with ionizing radiation in an atmosphere of 500 ppm, more preferably 100 ppm, and most preferably 50 ppm or less.

  It is also preferable to heat in an atmosphere of low oxygen concentration simultaneously and / or continuously with ionizing radiation irradiation. In particular, it is preferable that the low refractive index layer which is the outermost layer and is thin is cured by this method. The curing reaction is accelerated by heat, and a film having excellent physical strength and chemical resistance can be formed.

  In the present invention, at least one layer laminated on the transparent support can be cured by multiple times of ionizing radiation. In this case, it is preferable that at least two ionizing radiations are performed in a continuous reaction chamber in which the oxygen concentration does not exceed 1000 ppm. By performing multiple times of ionizing radiation irradiation in the same low oxygen concentration reaction chamber, the reaction time required for curing can be effectively ensured. In particular, when the production rate is increased for high productivity, ionizing radiation irradiation is required multiple times to ensure the energy of ionizing radiation necessary for the curing reaction.

  Further, when the curing rate (100-residual functional group content) is a certain value of less than 100%, the curing rate of the lower layer is obtained when a layer is provided thereon and cured by ionizing radiation and / or heat. Is higher than before the upper layer is provided, and the adhesion between the lower layer and the upper layer is improved, which is preferable.

[handling]
In order to continuously produce the antiglare film of the present invention, a process of continuously feeding a roll-shaped transparent support film, a process of applying and drying a coating liquid, a process of curing a coating film, a cured layer A step of winding the support film having the following is performed.

<Optical compensation area>
The optical compensation region of the liquid crystal display device of the present invention will be described.
The liquid crystal display device of the present invention has an optical compensation region between the first polarizing film and the liquid crystal cell. The optical compensation region preferably includes at least one first retardation region that satisfies any of the following formulas (A) to (D).
(A) 100 nm ≦ Re ≦ 400 nm and −50 nm ≦ Rth ≦ 50 nm
(B) 60 nm ≦ Re ≦ 200 nm and 30 nm ≦ Rth ≦ 100 nm
(C) 0 nm ≦ Re ≦ 20 nm and −400 nm ≦ Rth ≦ −50 nm
(D) 30 nm ≦ Re ≦ 150 nm and 100 nm ≦ Rth ≦ 400 nm
(Here, Re is in-plane retardation, and Rth is retardation in the thickness direction.)

  Furthermore, the liquid crystal display device of the present invention is more preferably the first or second embodiment described below, and the second embodiment is particularly preferable.

<First Embodiment>
Hereinafter, embodiments of the present invention will be described in detail with reference to the drawings. FIG. 5 is a schematic diagram showing an example of a pixel region of the liquid crystal display device of the present invention. 6 and 7 are schematic views of the first embodiment of the liquid crystal display device of the present invention.
The liquid crystal display device shown in FIG. 6 includes polarizing films 103 and 108, a first retardation region 111, and a liquid crystal cell 106. The polarizing films 103 and 108 are sandwiched between protective films 101 and 104 and 107 and 110, respectively.
In the present invention, the protective film 101 is a first protective film, the protective film 110 is a second protective film, and an antiglare layer is coated on either the first protective film or the second protective film. When the anti-glare layer is coated on the first protective film 101, the first protective film 101 is on the viewing side, and the second protective film 110 is on the back side. Moreover, when the glare-proof layer is coated on the 2nd protective film 110, the 2nd protective film 110 becomes a visual recognition side, and the 1st protective film 101 becomes a back side.

  In the liquid crystal display device of FIG. 6, the liquid crystal cell 106 includes a substrate (not shown in FIG. 6) and a liquid crystal layer (not shown in FIG. 6). The product Δn · d of the thickness d (μm) of the liquid crystal layer and the refractive index anisotropy Δn is optimal in the range of 0.2 to 0.4 μm for the IPS type having no twisted structure in the transmission mode. In this range, the white display luminance is high and the black display luminance is small, so that a bright and high-contrast display device can be obtained. An alignment film (not shown in FIG. 6) is formed on the surface of the substrate in contact with the liquid crystal layer, and the rubbing process is performed on the alignment film while aligning liquid crystal molecules substantially parallel to the surface of the substrate. Depending on the direction, the direction of liquid crystal molecule alignment in a state where no voltage is applied or in a state where a voltage is low is controlled, and the direction of the slow axis 105 is determined. An electrode (not shown in FIG. 6) capable of applying a voltage to the liquid crystal molecules is formed on the inner surface of the substrate.

FIG. 5 schematically shows the orientation of the liquid crystal molecules in one pixel region of the liquid crystal cell 106. FIG. 5 shows the alignment of liquid crystal molecules in a very small area corresponding to one pixel of the liquid crystal cell 106 in the rubbing direction 204 of the alignment film formed on the inner surfaces of the pair of substrates in the liquid crystal cell. It is the schematic diagram shown with the electrodes 202 and 203 which can apply a voltage to the liquid crystal molecule formed in the inner surface of a pair of board | substrate. When active driving is performed using a nematic liquid crystal having positive dielectric anisotropy as a field effect liquid crystal, the liquid crystal molecule alignment directions in a no-voltage application state or a low application state are 205a and 205b. A display is obtained. When applied between the electrodes 202 and 203, the liquid crystal molecules change their alignment direction in the direction of 206a and 206b according to the voltage. Usually, bright display is performed in this state.
The liquid crystal cell used in the present invention is not limited to the IPS mode, and any liquid crystal display device in which liquid crystal molecules are aligned substantially parallel to the surfaces of the pair of substrates during black display can be used. It can be used suitably. Examples thereof include a ferroelectric liquid crystal display device, an antiferroelectric liquid crystal display device, and an ECB type liquid crystal display device.

  In FIG. 6 again, the absorption axis 102 of the polarizing film 103 and the absorption axis 109 of the polarizing film 108 are arranged orthogonally. Further, the slow axis 112 of the first phase difference region 111 is arranged orthogonal to the absorption axis 102 of the polarizing film 103. Further, the absorption axis 102 of the polarizing film 103 and the slow axis 105 of the liquid crystal cell during black display are parallel, that is, the slow axis 112 of the first retardation region 111 and the slow axis of the liquid crystal cell during black display. The phase axis 105 is orthogonal. In this aspect, the viewing angle characteristic of the liquid crystal cell is improved by arranging the first retardation region 111 exhibiting specific optical characteristics described later.

  In the liquid crystal display device illustrated in FIG. 6, the polarizing film 103 is sandwiched between the two protective films 101 and 104, but the protective film 104 may be omitted. However, when the protective film 104 is not arranged, the first retardation region needs to have a specific optical characteristic to be described later and also have a function of protecting the polarizing film 103. When the protective film 104 is disposed, the retardation Rth in the thickness direction of the protective film is preferably 40 nm or less. The polarizing film 108 is also sandwiched between the two protective films 110 and 107, but the protective film 107 on the side close to the liquid crystal cell 106 may not be provided. When the protective film 107 is disposed, the preferred range of retardation Rth in the thickness direction of the protective film is the same as that of the protective film 104. Moreover, it is preferable that the thickness of the protective film 104 and the protective film 107 is thin, and specifically, it is preferable that it is 60 micrometers or less.

  Another embodiment of the present invention is shown in FIG. 7, the same members as those in FIG. 6 are denoted by the same reference numerals, and detailed description thereof is omitted. In the liquid crystal display device shown in FIG. 7, only the slow axis direction 112 of the first phase difference region 111 is different from the liquid crystal display device shown in FIG. In this configuration, the slow axis of the first retardation region 111 is arranged in parallel with the absorption axis 102 of the polarizing film 103. Further, the absorption axis 102 of the polarizing film 103 and the slow axis 105 of the liquid crystal cell during black display are parallel, that is, the slow axis 112 of the first retardation region 111 and the slow axis of the liquid crystal cell during black display. It is parallel to the phase axis 105. In this aspect, the viewing angle characteristic of the liquid crystal cell is improved by arranging the first retardation region 111 exhibiting specific optical characteristics described later.

  Also in the liquid crystal display device of FIG. 7, as described above, the protective film 101 is the first protective film, the protective film 110 is the second protective film, and either the first protective film or the second protective film is antiglare. The protective film on the side where the antiglare layer is applied is the viewing side, and the other protective film is the back side. Further, the protective film 104 or the protective film 107 may be omitted. When the protective film 104 and / or the protective film 107 are disposed, the retardation Rth in the thickness direction of the protective film is preferably 40 nm or less. Further, the protective film 104 and the protective film 107 are preferably thin, and specifically, 60 μm or less.

  The liquid crystal display device of the present invention is not limited to the configuration shown in FIGS. 5 to 7 and may include other members. For example, a color filter may be disposed between the liquid crystal layer and the polarizing film. When used as a transmission type, a cold cathode or a hot cathode fluorescent tube, or a backlight having a light emitting diode, a field emission element, or an electroluminescent element as a light source can be disposed on the back surface.

  Hereinafter, preferred optical characteristics of various members usable in the liquid crystal display device of the present invention, materials used for the members, manufacturing methods thereof, and the like will be described in detail.

[First phase difference region]
In the liquid crystal display device of the first embodiment shown in FIG. 6 or 7 of the present invention, the first retardation region satisfies the condition (A). That is, the in-plane retardation Re is 100 nm to 400 nm, and the retardation Rth in the thickness direction is −50 nm to 50 nm.
In order to effectively reduce light leakage in an oblique direction, Re in the first phase difference region is more preferably 105 nm to 250 nm, and further preferably 110 nm to 190 nm. Further, the value Nz is preferably 0.45 to 0.55, and more preferably 0.48 to 0.52.

  Examples of the retardation film having such optical properties include a birefringent film of a polymer film and an alignment film of a liquid crystal polymer.

  Examples of the polymer include polyolefins such as polystyrene, polycarbonate, and polypropylene, polyesters such as polyethylene terephthalate and polyethylene naphthalate, alicyclic polyolefins such as polynorbornene, polyvinyl alcohol, polyvinyl butyral, polymethyl vinyl ether, and polyhydroxyethyl acrylate. , Hydroxyethyl cellulose, hydroxypropyl cellulose, methyl cellulose, polyarylate, polysulfone, polyether sulfone, polyphenylene sulfide, polyphenylene oxide, polyallyl sulfone, polyamide, polyimide, polyvinyl chloride, cellulosic polymer, or a binary system thereof, Examples include ternary various copolymers, graft copolymers, blends, and the like. The retardation film controls the refractive index in the thickness direction by a method of stretching a polymer film biaxially in the plane direction, a method of stretching uniaxially or biaxially in the plane direction, and stretching in the thickness direction, etc. Can be obtained. Further, it can be obtained by, for example, a method in which a heat-shrinkable film is adhered to a polymer film and the polymer film is stretched or / and contracted by tilting under the action of the shrinkage force by heating.

  Examples of the liquid crystalline polymer include various main chain types and side chain types in which a conjugated linear atomic group (mesogen) imparting liquid crystal alignment is introduced into the main chain or side chain of the polymer. It is done. Specific examples of the main chain type liquid crystalline polymer include, for example, a nematic alignment polyester liquid crystalline polymer, a discotic polymer, and a cholesteric polymer having a structure in which a mesogen group is bonded to a spacer portion that imparts flexibility. . Specific examples of the side chain type liquid crystalline polymer include polysiloxane, polyacrylate, polymethacrylate, or polymalonate as a main chain skeleton, and a nematic alignment imparting paraffin through a spacer portion composed of a conjugated atomic group as a side chain. Examples thereof include those having a mesogen moiety composed of a substituted cyclic compound unit. The alignment film of these liquid crystalline polymers is, for example, a liquid crystalline polymer on an alignment-treated surface such as a surface of a thin film such as polyimide or polyvinyl alcohol formed on a glass plate, or an oblique deposition of silicon oxide. A solution in which the liquid crystal polymer is oriented by developing and heat-treating the above solution, and particularly in a tilted orientation, is preferred.

  Among these, a cellulose ester film such as a cellulose acylate film, a norbornene film, a polycarbonate film, a polyester film, or a polysulfone film is preferable.

  The thickness of the retardation film is preferably 1 to 300 μm, more preferably 10 to 200 μm, and still more preferably 20 to 150 μm.

<Second Embodiment>
Hereinafter, the present invention and the second embodiment will be described in detail with reference to the drawings. 8 and 9 are schematic views of the liquid crystal display device according to the second embodiment of the present invention.
The liquid crystal display device illustrated in FIG. 8 includes polarizing films 103 and 108, a first retardation region 111, a second retardation region 113, a substrate, and a liquid crystal layer sandwiched between the substrates. The configuration of the liquid crystal cell and the alignment state of the liquid crystal molecules in one pixel region of the liquid crystal layer are the same as those of the first embodiment of the liquid crystal display device of the present invention.
Polarizing films 103 and 108 are sandwiched between protective films 101 and 104 and 107 and 110, respectively. The absorption axis 102 of the polarizing film 103 and the transmission axis 109 of the polarizing film 108 are arranged orthogonally. The slow axis 112 of the first retardation region 111 is orthogonal to the absorption axis of the polarizing film 103 and parallel to the slow axis direction 106 of the liquid crystal cell during black display.
In the liquid crystal display device illustrated in FIG. 8, the polarizing film 103 is sandwiched between the two protective films 101 and 104, but the protective film 104 may be omitted. Further, although the polarizing film 108 is also sandwiched between the two protective films 107 and 110, the protective film 107 on the side close to the liquid crystal layer 108 may be omitted.
Also in the second aspect, an antiglare layer is applied to either the first protective film 101 or the second protective film 110, and the protective film provided with the antiglare layer is on the viewing side. The other protective film is on the back side. When the antiglare layer is coated on the first protective film 101, the first retardation region and the second retardation region are disposed between the liquid crystal cell and the viewing-side polarizing film. When the anti-glare layer is coated on the second protective film 110, the first retardation region and the second retardation region are disposed between the liquid crystal cell and the polarizing film on the back side. Become.

Another embodiment of the present invention is shown in FIG. In the liquid crystal display device of FIG. 9, the second retardation region 113 is disposed between the polarizing film 103 and the first retardation region 111. In the liquid crystal display device of FIG. 9, 101 is a first protective film, 110 is a second protective film, and an antiglare layer is applied to either the first protective film or the second protective film. The protective film on which the glare layer is coated is the viewing side, and the other protective film is the back side. As in the case of FIG. 8, the protective film 104 and / or the protective film 107 may be omitted.
In the embodiment shown in FIG. 9, the first retardation region 111 is arranged so that its slow axis 112 is parallel to the absorption axis of the polarizing film 103 and the slow axis 106 of the liquid crystal cell during black display. .

  Similarly to the liquid crystal display device according to the first aspect, the liquid crystal display device according to the second aspect of the present invention is not limited to the configuration shown in FIGS. 8 and 9, and may include other members.

  Hereinafter, preferred optical characteristics of various members usable in the liquid crystal display device of the present invention, materials used for the members, manufacturing methods thereof, and the like will be described in detail.

[First phase difference region]
The first phase difference region included in the second embodiment of the present invention satisfies the condition (B) or (D).
When the first retardation region satisfies the condition (B), the in-plane retardation Re is 60 nm to 200 nm, and the retardation Rth in the thickness direction is 30 nm to 100 nm. In order to effectively reduce the light leakage in the oblique direction, Re of the first phase difference region is more preferably 80 nm to 180 nm, and further preferably 90 nm to 160 nm. Moreover, it is preferable that Nz is 1.0-2.5, It is more preferable that it is 1.0-2.0, It is further more preferable that it is 1.0-1.8.

  When the first retardation region satisfies the condition (D), the in-plane retardation Re is 30 nm to 150 nm, and the retardation Rth in the thickness direction is 100 nm to 400 nm. In order to effectively reduce the light leakage in the oblique direction, Re of the first phase difference region is more preferably 40 nm to 115 nm, and further preferably 60 nm to 95 nm. Further, Nz is 1.5 to 7, and in order to effectively reduce light leakage in the oblique direction, Nz in the first phase difference region is more preferably 2.0 to 5.5. More preferably, it is 2.5-4.5.

  Basically, the material and form of the first retardation region are not particularly limited as long as it has the optical characteristics. For example, a retardation film made of a birefringent polymer film, a film obtained by applying a high molecular compound on a transparent support and then heated and salted, and a low molecular weight or high molecular liquid crystalline compound applied or transferred onto the transparent support Any of the retardation films having the retardation layer formed can be used. Moreover, each can also be laminated | stacked and used.

  The birefringent polymer film is preferably a film having excellent controllability of birefringence characteristics, transparency and heat resistance. In this case, the polymer material to be used is not particularly limited as long as it is a polymer capable of achieving uniform biaxial orientation, but is preferably a conventionally known material that can be formed by a solution casting method or an extrusion method, and is preferably a norbornene-based material. Examples include polymers, polycarbonate polymers, polyarylate polymers, polyester polymers, aromatic polymers such as polysulfone, cellulose acylate, or polymers obtained by mixing two or more of these polymers. It is done.

The biaxial orientation of the film is a film made of the thermoplastic resin produced by an appropriate method such as an extrusion molding method or a casting film forming method, for example, a longitudinal stretching method using a roll, a transverse stretching method using a tenter, or a biaxial stretching method. For example, it can be achieved by performing a stretching treatment. In the longitudinal stretching method using the roll, an appropriate heating method such as a method using a heating roll, a method of heating an atmosphere, or a method of using them together can be adopted. In the biaxial stretching method using a tenter, an appropriate method such as a simultaneous biaxial stretching method using an all tenter method or a sequential biaxial stretching method using a roll tenter method can be employed.
Moreover, a thing with little orientation nonuniformity and phase difference nonuniformity is preferable. The thickness can be appropriately determined depending on the phase difference or the like, but is generally 1 to 300 μm, especially 10 to 200 μm, especially 20 to 150 μm from the viewpoint of thinning.

  As the norbornene-based polymer, norbornene and its derivatives, tetracyclododecene and its derivatives, dicyclopentadiene and its derivatives, methanotetrahydrofluorene and its monomers as a main component of a norbornene-based monomer polymer, Ring-opening polymer of norbornene monomer, ring-opening copolymer of norbornene monomer and other monomer capable of ring-opening copolymerization, addition polymer of norbornene monomer, copolymerizable with norbornene monomer Examples include addition copolymers with other monomers and hydrogenated products thereof. Among these, from the viewpoints of heat resistance, mechanical strength, and the like, a ring-opening polymer hydride of a norbornene monomer is most preferable. The molecular weight of the norbornene-based polymer, the polymer of the monocyclic olefin or the polymer of the cyclic conjugated diene is appropriately selected according to the purpose of use, but the cyclohexane solution (toluene solution if the polymer resin does not dissolve) The polyisoprene or polystyrene-equivalent weight average molecular weight measured by gel permeation chromatography is usually 5,000 to 500,000, preferably 8,000 to 200,000, more preferably 10,000 to 100,000. When the thickness is in the range, the mechanical strength of the film (A) and the moldability are highly balanced, which is preferable.

  The acyl group of cellulose acylate may be an aliphatic group or an allyl group, and is not particularly limited. They are, for example, alkyl carbonyl esters, alkenyl carbonyl esters, aromatic carbonyl esters, aromatic alkyl carbonyl esters, etc. of cellulose, each of which may further have a substituted group, and an ester having a total carbon number of 22 or less. Groups are preferred. These preferred cellulose acylates include acyl groups having a total carbon number of 22 or less in the ester moiety (for example, acetyl, propionyl, butyroyl, barrel, heptanoyl, octanoyl, decanoyl, dodecanoyl, tridecanoyl, hexadecanoyl, octadecanoyl, etc. ), Arylcarbonyl groups (acrylic, methacrylic, etc.), allylcarbonylkis (benzoyl, naphthaloyl etc.) and cinnamoyl groups. Among these, cellulose acetate, cellulose acetate propionate, cellulose acetate butyrate, cellulose acetate stearate, cellulose acetate benzoate, etc. are not particularly limited in the case of mixed esters, but preferably acetate is the total ester. It is preferable that it is 30 mol% or more.

  Among these, cellulose acylate is preferred, and photographic grades are particularly preferred, and commercially available photographic grades can be obtained with satisfactory quality such as viscosity average degree of polymerization and substitution degree. As manufacturers of photographic grade cellulose triacetate, Daicel Chemical Industries, Ltd. (for example, LT-20, 30, 40, 50, 70, 35, 55, 105, etc.), Eastman Kodak Company (for example, CAB-551) 0.01, CAB-551-0.02, CAB-500-5, CAB-381-0.5, CAB-381-02, CAB-381-20, CAB-321-0.2, CAP-504 0.2, CAP-482-20, CA-398-3, etc.), Coatles, Hoechst, etc., any of which can use photographic grade cellulose acylate. Further, for the purpose of controlling the mechanical properties and optical properties of the film, plasticizers, surfactants, retardation modifiers, UV absorbers and the like can be used in the future (reference material: JP-A No. 2002-277632). Publication, Unexamined-Japanese-Patent No. 2002-182215).

As a method for forming the transparent resin into a sheet or film, for example, either a heat-melt molding method or a solution casting method can be used. The hot melt molding method can be further classified into an extrusion molding method, a press molding method, an inflation molding method, an injection molding method, a blow molding method, a stretch molding method, etc. Among these methods, mechanical strength, surface In order to obtain a film excellent in accuracy and the like, the extrusion molding method, the inflation molding method, and the press molding method are preferable, and the extrusion molding method is most preferable. The molding conditions are appropriately selected depending on the purpose of use and the molding method. In the case of the heat-melt molding method, the cylinder temperature is preferably set in the range of preferably 100 to 400 ° C, more preferably 150 to 350 ° C. The thickness of the sheet or film is preferably 10 to 300 μm, more preferably 30 to 200 μm.
When the glass transition temperature of the transparent resin is Tg, the stretching of the sheet or film is preferably in a temperature range of Tg-30 ° C to Tg + 60 ° C, more preferably in a temperature range of Tg-10 ° C to Tg + 50 ° C. In at least one direction, the stretching ratio is preferably 1.01 to 2 times. The stretching direction may be at least one direction. However, when the sheet is obtained by extrusion molding, the direction is preferably the resin mechanical flow direction (extrusion direction). A free shrink uniaxial stretching method, a fixed width uniaxial stretching method, a biaxial stretching method, and the like are preferable. The optical characteristics can be controlled by controlling the draw ratio and the heating temperature.

[Second phase difference region]
The second retardation region included in the liquid crystal display device according to the second embodiment of the present invention preferably satisfies the condition (C). That is, the in-plane retardation Re is preferably 0 nm to 20 nm, and the retardation Rth in the thickness direction is preferably −400 nm to −50 nm. A more preferable range of Rth in the second retardation region varies greatly depending on the first retardation region. First, when the retardation region satisfies the condition (B), Rth of the second retardation region is more preferably −300 nm to −100 nm, and further preferably −270 nm to −120 nm. First, when the retardation region satisfies the condition (C), Rth of the second retardation region is more preferably −400 nm to −80 nm, and further preferably −350 nm to −120 nm. preferable.
On the other hand, the in-plane retardation Re is preferably 0 nm to 20 nm, more preferably 0 nm to 10 nm, even more preferably 0 nm to 5 nm, regardless of whether the first retardation region satisfies the conditions (B) or (C). Is particularly preferred.

  As long as the second retardation region has the optical characteristics, the material and form thereof are not particularly limited. For example, a retardation film made of a birefringent polymer film and a retardation film having a retardation layer formed by applying or transferring a low molecular weight or high molecular liquid crystalline compound onto a transparent support are used. be able to. Moreover, each can also be laminated | stacked and used.

  The retardation film composed of a birefringent polymer film having the above optical characteristics is obtained by stretching a polymer film in the thickness direction of the film, or applying a vinylcarbazole polymer and drying it (Japanese Patent Laid-Open No. 2001-091746). Publication). In addition, as a retardation layer formed from a liquid crystalline compound having the above optical properties, a cholesteric discotic liquid crystal compound or composition containing a chiral structural unit is fixed after its helical axis is aligned substantially perpendicular to the substrate. For example, a layer formed by aligning a rod-like liquid crystal compound or composition having a positive refractive index anisotropy with a positive orientation to a substrate and then immobilizing the layer can be exemplified (for example, JP-A-6-6 331826 and Japanese Patent No. 2853064). The rod-like liquid crystal compound may be a low molecular compound or a high molecular compound. Furthermore, not only one retardation layer but also a plurality of retardation layers may be laminated to form the second retardation region exhibiting the above optical characteristics. Further, the second retardation region may be configured such that the entire laminated body of the support and the retardation layer satisfies the optical characteristics. As the rod-like liquid crystal compound to be used, those that take a nematic liquid crystal phase, a smectic liquid crystal phase, or a lyotropic liquid crystal phase in a temperature range in which the orientation is fixed are preferably used. A liquid crystal exhibiting a smectic A phase and a B phase capable of obtaining uniform vertical alignment without fluctuation is preferable. In particular, in the presence of an additive, a rod-like liquid crystalline compound that becomes a liquid crystal state in an appropriate orientation temperature range is formed by using a composition containing the additive and the rod-like liquid crystalline compound. Is also preferable.

《Bar-shaped liquid crystalline compound》
The second retardation region of the present invention may be formed from a composition containing a rod-like liquid crystal compound. Examples of the rod-like liquid crystalline compound include azomethines, azoxys, cyanobiphenyls, cyanophenyl esters, benzoic acid esters, cyclohexanecarboxylic acid phenyl esters, cyanophenylcyclohexanes, cyano-substituted phenylpyrimidines, alkoxy-substituted phenylpyrimidines. , Phenyldioxanes, tolanes and alkenylcyclohexylbenzonitriles are preferably used. In addition to the above low-molecular liquid crystalline molecules, high-molecular liquid crystalline molecules can also be used. As the liquid crystal molecules, those having a partial structure capable of causing polymerization or crosslinking reaction by actinic rays, electron beams, heat, or the like are preferably used. The number of the partial structures is 1 to 6, preferably 1 to 3.

  When the second retardation region includes a retardation layer formed by fixing the rod-like liquid crystalline compound in the aligned state, the rod-like liquid crystalline compound is substantially vertically aligned and fixed in that state. It is preferable to use a retardation layer. The term “substantially perpendicular” means that the angle formed between the film surface and the director of the rod-like liquid crystal compound is in the range of 70 ° to 90 °. These liquid crystalline compounds may be aligned obliquely or may be changed so that the inclination angle gradually changes (hybrid alignment). Even in the case of oblique orientation or hybrid orientation, the average inclination angle is preferably 70 ° to 90 °, more preferably 80 ° to 90 °, and most preferably 85 ° to 90 °.

  The retardation layer formed from the rod-like liquid crystalline compound is formed on the support with a coating liquid containing the rod-like liquid crystalline compound and, if desired, the following polymerizable initiator, air interface vertical alignment agent and other additives. It can be formed by coating on the vertical alignment film formed, vertically aligning, and fixing the alignment state. When it is formed on a temporary support, it can also be produced by transferring the retardation layer onto the support. Furthermore, not only a single retardation layer but also a plurality of retardation layers can be laminated to form a second retardation region exhibiting the above optical characteristics. Further, the second retardation region may be configured so that the entire laminated body of the support and the retardation layer satisfies the optical characteristics.

  As a solvent used for preparing the coating solution, an organic solvent is preferably used. Examples of organic solvents include amides (eg, N, N-dimethylformamide), sulfoxides (eg, dimethyl sulfoxide), heterocyclic compounds (eg, pyridine), hydrocarbons (eg, benzene, hexane), alkyl halides (eg, , Chloroform, dichloromethane), esters (eg, methyl acetate, butyl acetate), ketones (eg, acetone, methyl ethyl ketone), ethers (eg, tetrahydrofuran, 1,2-dimethoxyethane). Alkyl halides and ketones are preferred. Two or more organic solvents may be used in combination. The coating liquid can be applied by a known method (eg, extrusion coating method, direct gravure coating method, reverse gravure coating method, die coating method).

  The vertically aligned liquid crystal compound is preferably fixed while maintaining the alignment state. The immobilization is preferably performed by a polymerization reaction of the polymerizable group (P) introduced into the liquid crystal compound. The polymerization reaction includes a thermal polymerization reaction using a thermal polymerization initiator and a photopolymerization reaction using a photopolymerization initiator. A photopolymerization reaction is preferred. Examples of the photopolymerization initiator include α-carbonyl compounds (described in US Pat. Nos. 2,367,661 and 2,367,670), acyloin ether (described in US Pat. No. 2,448,828), α-hydrocarbon substituted aromatic acyloin. Compound (described in US Pat. No. 2,722,512), polynuclear quinone compound (described in US Pat. Nos. 3,046,127 and 2,951,758), a combination of triarylimidazole dimer and p-aminophenyl ketone (US Pat. No. 3,549,367) Description), acridine and phenazine compounds (JP-A-60-105667, U.S. Pat. No. 4,239,850) and oxadiazole compounds (U.S. Pat. No. 4,212,970).

The amount of the photopolymerization initiator used is preferably 0.01 to 20% by mass, more preferably 0.5 to 5% by mass, based on the solid content of the coating solution. The light irradiation for polymerizing the rod-like liquid crystalline molecules preferably uses ultraviolet rays. The irradiation energy is preferably ^{20mJ / cm 2 ~50J / cm 2} , further preferably 100 to 800 mJ / cm ^2. In order to accelerate the photopolymerization reaction, light irradiation may be performed under heating conditions. The thickness of the first retardation region including the optically illegal layer is preferably 0.1 to 10 μm, more preferably 0.5 to 5 μm, and most preferably 1 to 5 μm.

<< Vertical alignment film >>
In order to align the liquid crystalline compound vertically on the alignment film side, it is important to reduce the surface energy of the alignment film. Specifically, the surface energy of the alignment film is lowered by the functional group of the polymer, thereby bringing the liquid crystalline compound into a standing state. As the functional group for reducing the surface energy of the alignment film, a hydrocarbon group having 10 or more fluorine atoms and carbon atoms is effective. In order to make a fluorine atom or a hydrocarbon group exist on the surface of the alignment film, it is preferable to introduce a fluorine atom or a hydrocarbon group into the side chain rather than the main chain of the polymer. The fluoropolymer preferably contains fluorine atoms in a proportion of 0.05 to 80% by mass, more preferably in a proportion of 0.1 to 70% by mass, and in a proportion of 0.5 to 65% by mass. More preferably, it is most preferable to contain in the ratio of 1-60 mass%. The hydrocarbon group is an aliphatic group, an aromatic group or a combination thereof. The aliphatic group may be cyclic, branched or linear. The aliphatic group is preferably an alkyl group (may be a cycloalkyl group) or an alkenyl group (may be a cycloalkenyl group). The hydrocarbon group may have a substituent that does not exhibit strong hydrophilicity, such as a halogen atom. The number of carbon atoms of the hydrocarbon group is preferably 10 to 100, more preferably 10 to 60, and most preferably 10 to 40. The main chain of the polymer preferably has a polyimide structure or a polyvinyl alcohol structure.

  Polyimide is generally synthesized by a condensation reaction of tetracarboxylic acid and diamine. A polyimide corresponding to a copolymer may be synthesized using two or more kinds of tetracarboxylic acids or two or more kinds of diamines. The fluorine atom or hydrocarbon group may be present in the repeating unit derived from tetracarboxylic acid, may be present in the repeating unit derived from diamine, or may be present in both repeating units. When introducing a hydrocarbon group into polyimide, it is particularly preferable to form a steroid structure in the main chain or side chain of the polyimide. The steroid structure present in the side chain corresponds to a hydrocarbon group having 10 or more carbon atoms, and has a function of vertically aligning the liquid crystalline compound. In this specification, the steroid structure is a cyclopentanohydrophenanthrene ring structure or a ring structure in which a part of the ring bond is a double bond in the range of an aliphatic ring (a range that does not form an aromatic ring). means.

  Further, as a means for vertically aligning the liquid crystalline compound, a method of mixing an organic acid with a polymer of polyvinyl alcohol, modified polyvinyl alcohol, or polyimide can be suitably used. As the acid to be mixed, carboxylic acid, sulfonic acid and amino acid are preferably used. You may use what shows the acidity among the below-mentioned air interface aligning agent. Moreover, quaternary ammonium salts can also be used suitably. The mixing amount is preferably 0.1% by mass to 20% by mass and more preferably 0.5% by mass to 10% by mass with respect to the polymer.

  The saponification degree of the polyvinyl alcohol is preferably 70 to 100%, more preferably 80 to 100%. The polymerization degree of polyvinyl alcohol is preferably 100 to 5000.

  When aligning a rod-like liquid crystalline compound, the alignment film is preferably made of a polymer having a hydrophobic group as a functional group in the side chain. The specific type of functional group is determined according to the type of liquid crystal molecule and the required alignment state. For example, the modifying group of the modified polyvinyl alcohol can be introduced by copolymerization modification, chain transfer modification or block polymerization modification. Examples of modifying groups include hydrophilic groups (carboxylic acid groups, sulfonic acid groups, phosphonic acid groups, amino groups, ammonium groups, amide groups, thiol groups, etc.), hydrocarbon groups having 10 to 100 carbon atoms, fluorine atoms Substituted hydrocarbon groups, thioether groups, polymerizable groups (unsaturated polymerizable groups, epoxy groups, azirinidyl groups, etc.), alkoxysilyl groups (trialkoxy, dialkoxy, monoalkoxy) and the like can be mentioned. Specific examples of these modified polyvinyl alcohol compounds include, for example, paragraph numbers [0022] to [0145] in JP-A No. 2000-155216 and paragraph numbers [0018] to [0018] in JP-A No. 2002-62426. And the like described in [0022].

  The alignment film is formed by using a polymer having a side chain having a crosslinkable functional group bonded to the main chain or a polymer having a crosslinkable functional group on a side chain having a function of aligning liquid crystal molecules. When the retardation film is formed using a composition containing a polyfunctional monomer, the polymer in the alignment film and the polyfunctional monomer in the retardation film formed thereon can be copolymerized. As a result, a covalent bond is formed not only between the polyfunctional monomers but also between the alignment film polymers and between the polyfunctional monomer and the alignment film polymer, and the alignment film and the retardation film are firmly bonded. Therefore, the strength of the optical compensation sheet can be remarkably improved by forming the alignment film using a polymer having a crosslinkable functional group. The crosslinkable functional group of the alignment film polymer preferably contains a polymerizable group in the same manner as the polyfunctional monomer. Specific examples include those described in paragraphs [0080] to [0100] in JP-A-2000-155216.

  Apart from the crosslinkable functional group, the alignment film polymer can also be crosslinked using a crosslinking agent. Examples of the crosslinking agent include aldehydes, N-methylol compounds, dioxane derivatives, compounds that act by activating carboxyl groups, active vinyl compounds, active halogen compounds, isoxazole and dialdehyde starch. Two or more kinds of crosslinking agents may be used in combination. Specific examples include compounds described in paragraphs [0023] to [0024] in JP-A-2002-62426. Aldehydes having high reaction activity, particularly glutaraldehyde are preferred.

  0.1-20 mass% is preferable with respect to a polymer, and, as for the addition amount of a crosslinking agent, 0.5-15 mass% is more preferable. The amount of the unreacted crosslinking agent remaining in the alignment film is preferably 1.0% by mass or less, and more preferably 0.5% by mass or less. By adjusting in this way, even if the alignment film is used for a long time in a liquid crystal display device or left in a high-temperature and high-humidity atmosphere for a long time, sufficient durability without occurrence of reticulation can be obtained.

  The alignment film can be basically formed by applying a composition containing the polymer and the crosslinking agent, which are alignment film forming materials, onto a transparent support, followed by drying by heating (crosslinking) and rubbing treatment. it can. As described above, the crosslinking reaction may be performed at an arbitrary time after coating on the transparent support. When a water-soluble polymer such as polyvinyl alcohol is used as the alignment film forming material, the coating solution is preferably a mixed solvent of an organic solvent (eg, methanol) having a defoaming action and water. The ratio of water: methanol is preferably 0: 100 to 99: 1, and more preferably 0: 100 to 91: 9. Thereby, generation | occurrence | production of a bubble is suppressed and the defect of the alignment film and also the phase difference layer surface reduces remarkably.

  The alignment film is preferably applied by spin coating, dip coating, curtain coating, extrusion coating, rod coating, or roll coating. A rod coating method is particularly preferable. The film thickness after drying is preferably 0.1 to 10 μm. Heating and drying can be performed at 20 ° C to 110 ° C. In order to form sufficient cross-linking, 60 ° C to 100 ° C is preferable, and 80 ° C to 100 ° C is particularly preferable. The drying time can be 1 minute to 36 hours, preferably 1 minute to 30 minutes. The pH is preferably set to an optimum value for the crosslinking agent to be used. When glutaraldehyde is used, the pH is 4.5 to 5.5, and 5 is particularly preferable.

  The alignment film is preferably provided on the transparent support. The alignment film is used by crosslinking the polymer layer as described above. The rubbing treatment is preferably not performed for the vertical alignment of the rod-like liquid crystalline compound. In addition, after aligning a liquid crystalline compound using an alignment film, the liquid crystalline compound is fixed in the aligned state to form a retardation layer, and only the retardation layer is formed on the polymer film (or transparent support). You may transcribe.

《Air interface vertical alignment agent》
Usually, since the liquid crystalline compound has a property of being inclined and aligned on the air interface side, it is necessary to control the alignment of the liquid crystalline compound vertically on the air interface side in order to obtain a uniformly vertically aligned state. . For this purpose, a phase difference film is formed by adding a compound that is unevenly distributed on the air interface side and that has the effect of vertically aligning the liquid crystalline compound by its excluded volume effect or electrostatic effect to the liquid crystal coating liquid. It is preferable to do this.

  As the air interface alignment agent, compounds described in JP-A Nos. 2002-20363 and 2002-129162 can be used. In addition, paragraph numbers [0072] to [0075] of Japanese Patent Application Laid-Open No. 2004-053981, paragraph numbers [0037] to [0039] of Japanese Patent Application No. 2002-262239, paragraph number of Japanese Patent Application Laid-Open No. 2004-004688 [ [0078] to [0078], paragraph numbers [0052] to [0054], [0065] to [0066], [0092] to [0094] of JP 2004-139015 A, paragraphs of JP 2005-097357 A The matters described in the numbers [0028] to [0030] and paragraphs [0087] to [0090] of the specification of Japanese Patent Application No. 2004-003804 can also be appropriately applied to the present invention. Moreover, by mix | blending these compounds, applicability | paintability is improved and generation | occurrence | production of a nonuniformity or repellency is suppressed.

  The amount of the air interface alignment agent used in the liquid crystal coating liquid is preferably 0.05% by mass to 5% by mass. Moreover, when using a fluorine-type air interface aligning agent, it is preferable that it is 1 mass% or less.

<Other materials in retardation layer>
Along with the liquid crystal compound, a plasticizer, a surfactant, a polymerizable monomer, and the like can be used in combination to improve the uniformity of the coating film, the strength of the film, the orientation of the liquid crystal compound, and the like. These materials are preferably compatible with the liquid crystal compound and do not inhibit the alignment.

  Examples of the polymerizable monomer include radically polymerizable or cationically polymerizable compounds. Preferably, it is a polyfunctional radically polymerizable monomer and is preferably copolymerizable with the above-described polymerizable group-containing liquid crystal compound. Examples thereof include those described in paragraph numbers [0018] to [0020] in JP-A No. 2002-296423. The amount of the compound added is generally in the range of 1 to 50% by mass and preferably in the range of 5 to 30% by mass with respect to the discotic liquid crystalline molecules.

  Examples of the surfactant include conventionally known compounds, and fluorine compounds are particularly preferable. Specifically, for example, compounds described in paragraphs [0028] to [0056] in JP-A-2001-330725, and paragraphs [0069] to [0126] described in JP-A-2005-062673 Compounds.

  The polymer used together with the liquid crystal compound is preferably capable of thickening the coating solution. A cellulose ester can be mentioned as an example of a polymer. Preferable examples of the cellulose ester include those described in paragraph [0178] of JP-A No. 2000-155216. The addition amount of the polymer is preferably in the range of 0.1 to 10% by mass, and in the range of 0.1 to 8% by mass with respect to the liquid crystal molecules so as not to inhibit the alignment of the liquid crystal compound. It is more preferable.

[Protective film for polarizing film]
The liquid crystal display device of the present invention may have a polarizing film protective film for protecting the polarizing film. The protective film for polarizing film is preferably one that has no absorption in the visible light region, has a light transmittance of 80% or more, and has a small retardation based on birefringence. Specifically, the in-plane Re is preferably 0 to 30 nm, more preferably 0 to 15 nm, and most preferably 0 to 5 nm. Rth is preferably 40 nm or less, more preferably 40 nm to −50 nm, and even more preferably 20 nm to −20 nm.

  In addition, the thickness of the protective film, particularly the thickness of the protective film disposed on the liquid crystal cell side, is preferably 60 μm or less, more preferably 50 μm or less, and more preferably 40 μm or less from the viewpoint of reducing Rth. More preferably. However, when the protective film is composed of a plurality of layers in order to satisfy the above optical characteristics, the preferred range of thickness is not limited to this range.

As the protective film, any film satisfying the above properties can be suitably used. From the viewpoint of durability of the polarizing film, a cellulose acylate film, a norbornene-based film, or an acrylic film is used. It is preferably contained, and a cellulose acylate film or a norbornene-based film is more preferable.
As the norbornene-based polymer, norbornene and its derivatives, tetracyclododecene and its derivatives, dicyclopentadiene and its derivatives, methanotetrahydrofluorene and its monomers as a main component of a monomer polymer, Ring-opening polymer of norbornene monomer, ring-opening copolymer of norbornene monomer and other monomer capable of ring-opening copolymerization, addition polymer of norbornene monomer, copolymerizable with norbornene monomer Examples include addition copolymers with other monomers and hydrogenated products thereof. Among these, from the viewpoints of heat resistance, mechanical strength, and the like, a ring-opening polymer hydride of a norbornene monomer is most preferable. The molecular weight of the norbornene-based polymer, the polymer of the monocyclic olefin or the polymer of the cyclic conjugated diene is appropriately selected according to the purpose of use, but the cyclohexane solution (toluene solution if the polymer resin does not dissolve) The polyisoprene or polystyrene-equivalent weight average molecular weight measured by gel permeation chromatography is usually 5,000 to 500,000, preferably 8,000 to 200,000, more preferably 10,000 to 100,000. When the film thickness is in the range, the mechanical strength and moldability of the film are highly balanced and suitable.

  The cellulose acylate is not particularly limited, and the acyl group may be an aliphatic group or an allyl group. They are, for example, alkyl carbonyl esters, alkenyl carbonyl esters, aromatic carbonyl esters, aromatic alkyl carbonyl esters, etc. of cellulose, each of which may further have a substituted group, and an ester having a total carbon number of 22 or less. Groups are preferred. These preferred cellulose acylates include acyl groups having a total carbon number of 22 or less in the ester moiety (for example, acetyl, propionyl, butyroyl, barrel, heptanoyl, octanoyl, decanoyl, dodecanoyl, tridecanoyl, hexadecanoyl, octadecanoyl, etc. ), Arylcarbonyl groups (acrylic, methacrylic, etc.), allylcarbonylkis (benzoyl, naphthaloyl etc.) and cinnamoyl groups. Among these, cellulose acetate, cellulose acetate propionate, cellulose acetate butyrate, cellulose acetate stearate, cellulose acetate benzoate, etc. are not particularly limited in the case of mixed esters, but preferably acetate is the total ester. It is preferable that it is 30 mol% or more.

  Among these, cellulose acylate is preferred, and photographic grades are particularly preferred, and commercially available photographic grades can be obtained with satisfactory quality such as viscosity average degree of polymerization and substitution degree. As manufacturers of photographic grade cellulose triacetate, Daicel Chemical Industries, Ltd. (for example, LT-20, 30, 40, 50, 70, 35, 55, 105, etc.), Eastman Kodak Company (for example, CAB-551) 0.01, CAB-551-0.02, CAB-500-5, CAB-381-0.5, CAB-381-02, CAB-381-20, CAB-321-0.2, CAP-504 0.2, CAP-482-20, CA-398-3, etc.), Coatles, Hoechst, etc., any of which can use photographic grade cellulose acylate. In addition, a plasticizer, a surfactant, a retardation modifier, a UV absorber, and the like can be mixed for the purpose of controlling the mechanical properties and optical properties of the film (reference material: JP-A No. 2002-277632). Publication, Unexamined-Japanese-Patent No. 2002-182215).

As a method for forming the transparent resin into a sheet or film, for example, any of the hot melt molding method and the solution casting method can be used. The heat-melt molding method can be further classified into an extrusion molding method, a press molding method, an inflation molding method, an injection molding method, a blow molding method, a stretch molding method, etc. Among these methods, mechanical strength, surface In order to obtain a film excellent in accuracy and the like, an extrusion molding method, an inflation molding method and a press molding method are preferable, and an extrusion molding method is most preferable. The molding conditions are appropriately selected depending on the purpose of use and the molding method. In the case of the heat-melt molding method, the cylinder temperature is preferably set in the range of preferably 100 to 400 ° C, more preferably 150 to 350 ° C. The thickness of the sheet or film is preferably 10 to 300 μm, more preferably 30 to 200 μm.
When the glass transition temperature of the transparent resin is Tg, the stretching of the sheet or film is preferably in a temperature range of Tg-30 ° C to Tg + 60 ° C, more preferably in a temperature range of Tg-10 ° C to Tg + 50 ° C. In at least one direction, the stretching ratio is preferably 1.01 to 2 times. The stretching direction may be at least one direction, but when the sheet is obtained by extrusion, the direction is preferably the mechanical flow direction (extrusion direction) of the resin. A free shrink uniaxial stretching method, a fixed width uniaxial stretching method, a biaxial stretching method, and the like are preferable. The optical characteristics can be controlled by controlling the draw ratio and the heating temperature.

  As a method for reducing the Rth of the cellulose acylate film, it is effective to mix a non-planar structure compound into the film. Moreover, the method of Unexamined-Japanese-Patent No. 11-246704, Unexamined-Japanese-Patent No. 2001-247717, Japanese Patent Application No. 2003-379975, etc. are mentioned. Rth can also be reduced by reducing the thickness of the cellulose acylate film.

  A polarizing plate protective film having negative optical characteristics for Rth is obtained by a method of stretching a polymer film in the thickness direction of the film (eg, JP-A No. 2000-162436) or a method of applying and drying a vinylcarbazole polymer. (Example: JP-A-2001-091746) can be easily formed. Further, the protective film may contain a liquid crystal material, and for example, may be a retardation layer formed from a liquid crystalline compound having Rth negative optical characteristics. The retardation layer is a layer formed by fixing a cholesteric discotic liquid crystal compound or composition containing a chiral structural unit with its helical axis aligned substantially perpendicular to the substrate, and having a positive refractive index anisotropy. Examples thereof include a layer formed by orienting the rod-like liquid crystal compound or composition of the present invention after being oriented substantially perpendicularly to the substrate and the like (see, for example, JP-A-6-331826 and Japanese Patent No. 2853064). The rod-like liquid crystal compound may be a low molecular compound or a high molecular compound. Furthermore, it is possible to form a protective film that exhibits not only one retardation layer but also a plurality of retardation layers to exhibit optical characteristics with negative Rth. Further, the protective layer may be configured so that the entire laminate of the support and the retardation layer satisfies a negative optical characteristic of Rth. As the rod-like liquid crystal compound to be used, those that take a nematic liquid crystal phase, a smectic liquid crystal phase, or a lyotropic liquid crystal phase in a temperature range in which the orientation is fixed are preferably used. A liquid crystal exhibiting a smectic A phase and a B phase capable of obtaining uniform vertical alignment without fluctuation is preferable. In particular, in the presence of an additive, a rod-like liquid crystalline compound that becomes a liquid crystal state in an appropriate orientation temperature range is formed by using a composition containing the additive and the rod-like liquid crystalline compound. Is also preferable.

  In order to improve adhesion between the protective film and the layer (adhesive layer, alignment film or retardation layer) provided thereon, the film is subjected to surface treatment (eg, glow discharge treatment, corona discharge treatment, ultraviolet (UV) treatment, flame) Processing) may be performed. An adhesive layer (undercoat layer) may be provided on the transparent support. Moreover, the average particle diameter is 10 to 100 nm in order to provide the transparent support or the long transparent support with slipperiness in the conveying process or to prevent the back surface and the surface from sticking after winding. It is preferable to use what formed the polymer layer which mixed the inorganic particle of about 5%-40% by solid content mass ratio on the one side of the support body by application | coating or co-casting with a support body.

[Saponification]
In the present invention, the antiglare film is one of the two surface protective films of the polarizing film. When producing a polarizing plate, it is preferable to improve the adhesiveness in an adhesive surface by hydrophilizing the surface on the side bonded to a polarizing film.

<Polarizing plate>
[Configuration of polarizing plate]
In the present invention, the antiglare film can be used as one or both of the protective film of the polarizing film composed of the polarizing film and the protective film disposed on both sides thereof to form an antiglare polarizing plate. .

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

  Furthermore, in the polarizing plate of the present invention, one side is the antiglare film of the present invention, whereas the other protective film is an optical compensation film having an optically anisotropic layer made of a liquid crystalline compound. This is a preferred embodiment.

[Polarizing film]
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 film traveling direction at the exit of the step of holding the film both ends and the substantial stretching direction of the film is inclined by 20 to 70 °. In addition, the film traveling direction can be produced by a stretching method in which the film is bent while both ends of the film are held. 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.

  In the present invention, the transparent support of the antiglare film or the slow axis of the cellulose acetate film and the transmission axis of the polarizing film are preferably arranged so as to be substantially parallel.

  The features of the present invention will be described more specifically with reference to examples and comparative examples. The materials, amounts used, ratios, processing details, processing procedures, and the like shown in the following examples can be changed as appropriate without departing from the spirit of the present invention. Therefore, the scope of the present invention should not be construed as being limited by the specific examples shown below. Unless otherwise specified, “part” and “%” are based on mass.

<Preparation of IPS mode liquid crystal cell 1>
As shown in FIG. 5, electrodes (202 and 203 in FIG. 5) are arranged on a glass substrate so that the distance between adjacent electrodes is 20 μm, and a polyimide film is used as an alignment film on the glass substrate. A rubbing process was performed. A rubbing process was performed in a direction 204 shown in FIG. A polyimide film was provided on one surface of a separately prepared glass substrate, and a rubbing treatment was performed to obtain an alignment film. The two glass substrates are stacked and bonded so that the alignment films face each other, the distance between the substrates (gap; d) is 3.9 μm, and the rubbing directions of the two glass substrates are parallel. A nematic liquid crystal composition having a refractive index anisotropy (Δn) of 0.0769 and a dielectric anisotropy (Δε) of 4.5 was enclosed. The value of d · Δn of the liquid crystal layer was 300 nm.

<Preparation of the first retardation region 1>
Polymer film containing polycarbonate resin having a thickness of 55 μm [trade name “Elmec” manufactured by Kaneka Corporation (mass average molecular weight = 60,000, average refractive index = 1.53, Tg = 136 ° C., Re [590] = 1.0 nm, Rth [590] = 3.0 nm)] on both sides of a shrinkable film (biaxially stretched film containing polypropylene having a thickness of 60 μm [trade name “Treffan BO2570A” manufactured by Toray Industries, Inc.]) It bonded together through the system adhesive layer (thickness 15 micrometers). Thereafter, the film longitudinal direction is maintained with a roll stretching machine, and stretched 1.26 times in an air circulation oven at 147 ° C. After stretching, the shrinkable film is peeled off together with the acrylic pressure-sensitive adhesive layer, An optical compensation film A corresponding to the first retardation region 1 was produced. In the first phase difference region 1, the refractive index ellipsoid showed a relationship of nx>nz> ny.

  Using an automatic birefringence meter (KOBRA-21ADH, manufactured by Oji Scientific Instruments Co., Ltd.), the light incident angle dependence of Re in the first phase difference region 1 was measured and the optical characteristics thereof were calculated. 270 nm, Rth was 0 nm, and Nz was 0.50. Therefore, the first phase difference region 1 satisfies the condition of the formula (A).

<Preparation of the first retardation region 2>
The following composition was put into a mixing tank and stirred while heating to dissolve each component to prepare a cellulose acetate solution. The solution was filtered using a filter paper (No. 63, manufactured by Advantech) having a retained particle diameter of 4 μm and a drainage time of 35 seconds at 5 kg / cm ² or less.

[Cellulose acetate solution composition]
Cellulose acetate having an acetylation degree of 60.9% (polymerization degree 300, Mn / Mw = 1.5) 100 parts by mass triphenyl phosphate (plasticizer) 7.8 parts by mass biphenyl diphenyl phosphate (plasticizer) 3.9 parts by mass Methylene chloride (first solvent) 300 parts by mass Methanol (second solvent) 54 parts by mass 1-butanol (third solvent) 11 parts by mass

  In another mixing tank, 8 parts by mass of the following retardation increasing agent A, 10 parts by mass of retardation increasing agent B, 0.28 parts by mass of silicon dioxide fine particles (average particle size: 0.1 μm), 80 parts by mass of methylene chloride And 20 parts by mass of methanol were added and stirred while heating to prepare a retardation increasing agent solution (and a fine particle dispersion). The dope was prepared by mixing 474 parts by mass of the cellulose acetate solution with 40 parts by mass of the retardation increasing agent solution and stirring sufficiently.

  The obtained dope was cast using a band casting machine. A film having a residual solvent amount of 15% by mass was stretched transversely at a stretch ratio of 20% using a tenter under the conditions of 130 ° C., held at 50 ° C. for 30 seconds with the stretched width, and then clipped to remove cellulose. An acetate film was prepared. The residual solvent amount at the end of stretching was 5% by mass, and further dried to prepare a film with the residual solvent amount being less than 0.1% by mass.

  The thickness of the film thus obtained (first retardation region 2) was 80 μm. About the produced 1st phase difference area | region 2, Re is 70 nm by measuring the light incident angle dependence of Re using an automatic birefringence meter (KOBRA-21ADH, Oji Scientific Instruments Co., Ltd. product). It was found that Rth was 175 nm and Nz was 3.0. Accordingly, the first phase difference region 2 satisfies the condition (D).

<Preparation of Second Phase Difference Region 1>
(Saponification)
The cellulose acylate film corresponding to the first retardation region 2 produced above was passed through a dielectric heating roll having a temperature of 60 ° C., and the film surface temperature was raised to 40 ° C. After coating with a coater at 14 ml / m ² and heating for 10 seconds under a steam far infrared heater (manufactured by Noritake Co., Ltd.) heated to 110 ° C., 3 ml / m of pure water was also used using a bar coater. ² applied. The film temperature at this time was 40 degreeC. Next, washing with a fountain coater and draining with an air knife were repeated three times, and then the film was retained in a drying zone at 70 ° C. for 2 seconds to be dried.

<Alkaline solution composition>
Potassium hydroxide 4.7 parts by weight Water 15.7 parts by weight Isopropanol 64.8 parts by weight Propylene glycol 14.9 parts by weight C ₁₆ H ₃₃ O (CH ₂ CH ₂ O) ₁₀ H (surfactant) 1.0 mass Part

(Preparation of alignment film)
An alignment film coating solution having the following composition was continuously applied with a # 14 wire bar to the surface of the cellulose acylate film corresponding to the long first retardation region 2 produced above and subjected to saponification treatment. The alignment film was formed by drying with warm air of 60 ° C. for 60 seconds and further with warm air of 100 ° C. for 120 seconds.
Composition of Alignment Film Coating Solution (A1) The following modified polyvinyl alcohol 10 parts by mass Water 371 parts by mass Methanol 119 parts by mass Glutaraldehyde 0.5 parts by mass

  A coating liquid containing a rod-like liquid crystal compound having the following composition was continuously applied on the prepared alignment film with a wire bar. The conveyance speed of the film was 20 m / min. The solvent was dried in a step of continuously heating from room temperature to 80 ° C., and then heated in a drying zone at 80 ° C. for 90 seconds to align the rod-like liquid crystal compound. Subsequently, the temperature of the film was maintained at 60 ° C., the orientation of the liquid crystal compound was fixed by UV irradiation, and the second retardation region 1 was formed. Subsequently, the film prepared in a 1.5 mol / L sodium hydroxide aqueous solution at 55 ° C. was immersed for 2 minutes, and then immersed in water to sufficiently wash away sodium hydroxide. Then, after being immersed for 1 minute in 5 mmol / L sulfuric acid aqueous solution of 35 degreeC, it was immersed in water and the dilute sulfuric acid aqueous solution was fully washed away. Finally, the sample was thoroughly dried at 120 ° C. Thus, an optical compensation film B in which the first retardation region 2 and the second retardation region 1 were laminated was produced.

Composition of coating liquid (S1) containing rod-shaped liquid crystal compound The following rod-shaped liquid crystal compound (I) 100 parts by mass photopolymerization initiator (Irgacure 907, manufactured by Ciba Geigy) 3 parts by mass sensitizer (Kayacure DETX, Nippon Kayaku) 1 part by mass The following fluoropolymer 0.4 part by mass The following pyridinium salt 1 part by mass Methyl ethyl ketone 172 parts by mass

  Only the optically anisotropic layer (second retardation region 1) containing the rod-like liquid crystalline compound is peeled from the produced optical compensation film B, and an automatic birefringence meter (KOBRA-21ADH, manufactured by Oji Scientific Instruments) is used. The optical properties were measured. Re of only the optically anisotropic layer measured at a wavelength of 590 nm was 0 nm, and Rth was −225 nm. It was also confirmed that an optically anisotropic layer in which rod-like liquid crystal molecules were aligned substantially perpendicular to the film surface was formed. Therefore, the second phase difference region 1 satisfies the condition (C).

<Preparation of the first retardation region 3>
By uniaxially stretching a long norbornene-based resin film (manufactured by Nippon Zeon Co., Ltd .: trade name Zeooa: thickness 60 μm: photoelastic coefficient 3.10 × 10 ⁻¹² m ² / N) at 140 ° C. by 1.28 times, A long stretched film of the first retardation region 3 was produced.
The thickness of the first retardation region 3 was 35 μm, the in-plane retardation Re was 130 nm, and the thickness direction retardation Rth was 65 nm. Accordingly, the first phase difference region 3 satisfies the condition (B).

<Preparation of second retardation region 2>
The optical compensation film B was used on one surface of a long polyethylene terephthalate film (thickness: 100 μm) as a temporary support. The alignment film coating solution (A1) was continuously applied with a # 14 wire bar. The alignment film was formed by drying with warm air of 60 ° C. for 60 seconds and further with warm air of 100 ° C. for 120 seconds.

  The coating liquid (S1) containing the rod-like liquid crystal compound was continuously applied with a wire bar on the prepared alignment film. The conveyance speed of the film was 20 m / min. The solvent was dried in a step of continuously heating from room temperature to 80 ° C., and then heated in a drying zone at 80 ° C. for 90 seconds to align the rod-like liquid crystal compound. Subsequently, the temperature of the film was maintained at 60 ° C., the orientation of the liquid crystal compound was fixed by UV irradiation, and the second retardation region 2 was formed.

  Only the second retardation region 2 containing the rod-like liquid crystalline compound was peeled from the produced film, and the optical properties were measured using an automatic birefringence meter (KOBRA-21ADH, manufactured by Oji Scientific Instruments). Re of only the second retardation region 2 measured at a wavelength of 590 nm was 0 nm, and Rth was −160 nm. Therefore, the second phase difference region 2 satisfies the condition (C).

  A commercially available UV curable adhesive (UV-3400, manufactured by Toagosei Co., Ltd.) was applied on the second retardation region 2 obtained above (the surface opposite to the polyethylene terephthalate film), and the thickness was 5 μm. The adhesive layer 1 having a thickness is formed, and the stretched film of the first retardation region 3 prepared above is laminated thereon, and UV irradiation of about 600 mJ is performed from the first retardation region 3 side. The layer was cured. Thereafter, the first retardation region 3 / adhesive layer 1 / second retardation region 2 / polyethylene terephthalate film is peeled from the laminate in which the polyethylene terephthalate film is integrated, whereby the second retardation region 2 is removed. The film was transferred onto a stretched film that is one retardation region 3 to obtain an optical compensation film C composed of first retardation region 3 / adhesive layer 1 / second retardation region 2.

<Creation of the first phase difference region 4>
Film of cellulose ester with a thickness of 110 μm [manufactured by Kaneka, trade name: KA, DSac (acetyl substitution degree) = 0.04, DSpr (propionyl substitution degree) = 2.76], 1.5 times free end at 145 ° C. The first retardation 4 having a thickness of 108 μm was obtained by stretching. The in-plane retardation Re of the obtained first retardation region 4 was 140 nm, and the thickness direction retardation Rth was 75 nm. Therefore, the first phase difference region 4 satisfies the condition (B).

<Creation of second phase difference region 3>
After the saponification of the first retardation region 4 created above and the formation of the alignment film in the same manner as the first retardation region 2, the coating liquid (S1) containing the rod-like liquid crystal compound was used as the orientation film produced above. It was continuously applied on the top with a wire bar. The conveyance speed of the film was 20 m / min. The solvent was dried in a step of continuously heating from room temperature to 80 ° C., and then heated in a drying zone at 80 ° C. for 90 seconds to align the rod-like liquid crystal compound. Subsequently, the temperature of the film was maintained at 60 ° C., the orientation of the liquid crystal compound was fixed by UV irradiation, the second retardation region 3 was formed, and the optical compensation film D was created.

  Only the second retardation region 3 containing the rod-like liquid crystalline compound was peeled from the produced film, and the optical characteristics were measured using an automatic birefringence meter (KOBRA-21ADH, manufactured by Oji Scientific Instruments). Re of only the second retardation region 3 measured at a wavelength of 590 nm was 0 nm, and Rth was −160 nm. Therefore, the second phase difference region 3 satisfies the condition (C).

<Production of Polarizing Plate Protective Film 1>
(Polarizing plate protective film 1)
The following composition was put into a mixing tank, stirred while heating to dissolve each component, and a cellulose acetate solution A was prepared.
<Composition of cellulose acetate solution A>
Cellulose acetate with a degree of substitution of 2.86 100 parts by weight Triphenyl phosphate (plasticizer) 7.8 parts by weight Biphenyl diphenyl phosphate (plasticizer) 3.9 parts by weight methylene chloride (first solvent) 300 parts by weight methanol (second solvent) ) 54 parts by mass 1-butanol 11 parts by mass

The following composition was charged into another mixing tank, stirred while heating to dissolve each component, and an additive solution B-1 was prepared.
<Additive solution B-1 composition>
Methylene chloride 80 parts by mass Methanol 20 parts by mass The following optical anisotropy reducing agent 40 parts by mass

40 parts by mass of the additive solution B-1 was added to 477 parts by mass of the cellulose acetate solution A, and the dope was prepared by sufficiently stirring. The dope was cast from a casting port onto a drum cooled to 0 ° C. The film is peeled off at a solvent content of 70% by mass, and both ends in the width direction of the film are fixed with a pin tenter (the pin tenter described in FIG. 3 of JP-A-4-1009), and the solvent content is 3-5% by mass. In this state, the film was dried while maintaining an interval at which the stretching ratio in the transverse direction (direction perpendicular to the machine direction) was 3%. Then, it further dried by conveying between the rolls of the heat processing apparatus, and produced the polarizing plate protective film 1 with a thickness of 80 μm.
Using an automatic birefringence meter (KOBRA-21ADH, manufactured by Oji Scientific Instruments), the light incident angle dependence of Re was measured, and the optical characteristics were calculated. Re was 1 nm and Rth was 6 nm. Was confirmed.

<Preparation of polarizing plate A>
Next, iodine is adsorbed to the stretched polyvinyl alcohol film to produce a polarizing film, a commercially available cellulose acetate film (Fujitac TD80UF, manufactured by Fuji Film Co., Ltd.) is subjected to saponification treatment, and a polyvinyl alcohol adhesive is used. Affixed to one side of the polarizing film. Further, the polarizing plate protective film 1 was subjected to saponification treatment on the other side of the polarizing film, and was attached using a polyvinyl alcohol-based adhesive so that the cellulose acetate film side became the polarizing film side, thereby preparing the polarizing plate A.

<Preparation of polarizing plate B>
In the same manner, a polarizing film was produced, and a commercially available cellulose acylate film (Fujitac TD80UF, manufactured by Fuji Film Co., Ltd.) was saponified, and then adhered to both surfaces of the polarizing film using a polyvinyl alcohol adhesive. B was produced.

<Creation of antiglare film>
[Preparation of coating solution for each layer]
[Preparation of coating solution for antiglare layer]
Each component shown below was put into a mixing tank, stirred, and then filtered through a polypropylene filter having a pore size of 30 μm.

Composition of antiglare layer coating solution (HCL-1) “DPHA” 96.7 parts by mass “MX-1000” 0.3 parts by mass “Irgacure 184” 3.0 parts by mass Methyl isobutyl ketone 60.0 parts by mass Methyl ethyl ketone 40 .0 parts by mass

Composition of antiglare layer coating solution (HCL-2) “DPHA” 96.7 parts by mass Average particle size 3 μm PMMA particles 0.3 parts by mass “Irgacure 184” 3.0 parts by mass Methyl isobutyl ketone 60.0 parts by mass Methyl ethyl ketone 40 .0 parts by mass

Composition of antiglare layer coating solution (HCL-3) “DPHA” 96.7 parts by mass Average particle size 6 μm PMMA particles 0.3 parts by mass “Irgacure 184” 3.0 parts by mass Methyl isobutyl ketone 60.0 parts by mass Methyl ethyl ketone 40 .0 parts by mass

Composition of antiglare layer coating solution (HCL-4) “DPHA” 96.7 parts by mass Average particle size 12 μm PMMA particles 0.3 parts by mass “Irgacure 184” 3.0 parts by mass Methyl isobutyl ketone 60.0 parts by mass Methyl ethyl ketone 40 .0 parts by mass

Composition of antiglare layer coating solution (HCL-5) “DPHA” 96.7 parts by mass Average particle size 15 μm PMMA particles 0.3 parts by mass “Irgacure 184” 3.0 parts by mass Methyl isobutyl ketone 60.0 parts by mass Methyl ethyl ketone 40 .0 parts by mass

Composition of antiglare layer coating solution (HCL-6) “DPHA” 97.0 parts by mass “MX-1000” 0.01 parts by mass “Irgacure 184” 3.0 parts by mass Methyl isobutyl ketone 60.0 parts by mass Methyl ethyl ketone 40 .0 parts by mass

Composition of antiglare layer coating liquid (HCL-7) “DPHA” 96.95 parts by mass “MX-1000” 0.05 parts by mass “Irgacure 184” 3.0 parts by mass Methyl isobutyl ketone 60.0 parts by mass Methyl ethyl ketone 40 .0 parts by mass

Composition of antiglare layer coating solution (HCL-8) “DPHA” 96.9 parts by mass “MX-1000” 0.1 part by mass “Irgacure 184” 3.0 parts by mass Methyl isobutyl ketone 60.0 parts by mass Methyl ethyl ketone 40 .0 parts by mass

Composition of antiglare layer coating solution (HCL-9) “DPHA” 96.0 parts by mass “MX-1000” 1.0 part by mass “Irgacure 184” 3.0 parts by mass Methyl isobutyl ketone 60.0 parts by mass Methyl ethyl ketone 40 .0 parts by mass

Composition of antiglare layer coating solution (HCL-10) “DPHA” 94.0 parts by mass “MX-1000” 3.0 parts by mass “Irgacure 184” 3.0 parts by mass Methyl isobutyl ketone 60.0 parts by mass Methyl ethyl ketone 40 .0 parts by mass

(Preparation of sol liquid a-2)
In a 1,000 ml reaction vessel equipped with a thermometer, a nitrogen inlet tube and a dropping funnel, 187 g (0.80 mol) of acryloxyoxypropyltrimethoxysilane, 27.2 g (0.20 mol) of methyltrimethoxysilane, 320 g of methanol ( 10 mol) and 0.06 g (0.001 mol) of KF were added, and 15.1 g (0.86 mol) of water was slowly added dropwise at room temperature with stirring. After completion of the dropwise addition, the mixture was stirred at room temperature for 3 hours, and then heated and stirred for 2 hours under methanol reflux. Then, 120 g of sol liquid a-2 was obtained by depressurizingly distilling a low boiling point component and further filtering. As a result of GPC measurement of the substance thus obtained, the mass average molecular weight was 1500, and among the components higher than the oligomer component, the component having a molecular weight of 1000 to 20000 was 30%.
Moreover, from the measurement result of 1H-NMR, the structure of the obtained substance was a structure represented by the following general formula.

Furthermore, the condensation rate α as determined by ²⁹ Si-NMR was 0.56. From this analysis result, it was found that the silane coupling agent sol was mostly composed of a linear structure.
From the gas chromatography analysis, the raw material acryloxypropyltrimethoxysilane had a residual rate of 5% or less.

Composition of antiglare layer coating solution (HCL-11) PET-30 50.0 parts by mass Irgacure 184 2.0 parts by mass cross-linked acrylic-styrene particles (30%) 14.5 parts by mass sol liquid a-2 9.5 Part by weight toluene 38.5 parts by weight

Each of the above components is as follows.
“DPHA”: a mixture of dipentaerythritol pentaacrylate and dipentaerythritol hexaacrylate, refractive index 1.52, manufactured by Nippon Kayaku Co., Ltd.
PET-30: A mixture of pentaerythritol triacrylate and pentaerythritol tetraacrylate [manufactured by Nippon Kayaku Co., Ltd.]
“Irgacure 184”: photopolymerization initiator, manufactured by Ciba Specialty Chemicals “MX-1000”: polymethyl methacrylate fine particles, average particle size 10.0 μm, manufactured by Soken Chemical Co., Ltd. average particle size 3 μm PMMA particles: Particles having the same composition as MX-1000 and an average particle size of 3.0 μm.
Average particle size 6 μm PMMA particles: particles having the same composition as MX-1000 and an average particle size of 6.0 μm.
Average particle size 12 μm PMMA particles: Particles having the same composition as MX-1000 and an average particle size of 12.0 μm.
PMMA particles having an average particle size of 15 μm: particles having the same composition as MX-1000 and an average particle size of 12.0 μm.
“Crosslinked acrylic-styrene particles”: average particle size 3.5 μm, refractive index 1.53

[Preparation of coating solution for low refractive index layer]
(Preparation of sol solution a)
In a reactor equipped with a stirrer and a reflux condenser, 120 parts by mass of methyl ethyl ketone, 100 parts by mass of acryloxypropyltrimethoxysilane “KBM-5103” (manufactured by Shin-Etsu Chemical Co., Ltd.), 3 parts by mass of diisopropoxyaluminum ethyl acetoacetate After adding a part and mixing, 30 mass parts of ion-exchange water was added, and it was made to react at 60 degreeC for 4 hours, Then, it cooled to room temperature and obtained the sol liquid a. The mass average molecular weight was 1800, and among the components higher than the oligomer component, the component having a molecular weight of 1000 to 20000 was 100% by mass. From the gas chromatography analysis, the raw material acryloxypropyltrimethoxysilane did not remain at all.

{Preparation of hollow silica fine particle dispersion (A-1)}
Hollow silica fine particle sol (particle size of about 40 to 50 nm, shell thickness of 6 to 8 nm, refractive index of 1.31, solid content concentration of 20% by mass, main solvent isopropyl alcohol, according to Preparation Example 4 of JP 2002-79616 A 500 parts by mass, 30 parts by mass of acryloyloxypropyltrimethoxysilane “KBM-5103” {manufactured by Shin-Etsu Chemical Co., Ltd.}, and diisopropoxyaluminum ethyl acetoacetate “Kelope EP-12” “{Hope Pharmaceutical Co., Ltd.} 1.5 parts by mass was added and mixed, and then 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, 1.8 parts of acetylacetone was added, and the hollow silica dispersion liquid (A-1) was obtained. The resulting hollow silica dispersion had a solid content concentration of 18% by mass and a refractive index after solvent drying of 1.31.

{Preparation of coating solution for low refractive index layer (LL-1)}
44.0 parts by mass of a fluorine-containing copolymer (P-3) (mass average molecular weight of about 50000) described in JP-A-2004-45462, dipentaerythritol pentaacrylate and dipentaerythritol with respect to 100 parts by mass of methyl ethyl ketone Hexaacrylate mixture “DPHA” {manufactured by Nippon Kayaku Co., Ltd.} 6.0 parts by mass, terminal methacrylate group-containing silicone “RMS-033” (manufactured by Gelest) 3.0 parts by mass, “Irgacure 907” {Ciba 3.0 parts by mass of Specialty Chemicals Co., Ltd.} was added and dissolved. Thereafter, 195 parts by mass of the hollow silica fine particle dispersion (A-1) (39.0 parts by mass as the solid content of silica + surface treatment agent) and 17.2 parts by mass of the sol liquid a (5.0 parts by mass as the solid part) were added. Added. The coating liquid for low refractive index layer (LL-1) was prepared by diluting with cyclohexane and methyl ethyl ketone so that the solid content concentration of the entire coating liquid was 6% by mass and the ratio of cyclohexane and methyl ethyl ketone was 10:90.

[Preparation of antiglare film]
[Coating of anti-glare layer]
Using a slot die coater described in FIG. 1 of Japanese Patent Application Laid-Open No. 2003-211052, the 80 μm-thick triacetyl cellulose film “TAC-TD80U” (manufactured by FUJIFILM Corporation) is unwound in a roll form. The antiglare layer coating liquids (HCL-1) to (HCL-11) were applied so as to have the dry film thicknesses shown in Table 1 below, dried at 30 ° C. for 15 seconds and 90 ° C. for 20 seconds, and then further nitrogen. Using an “air-cooled metal halide lamp” (manufactured by Eye Graphics Co., Ltd.) of 160 W / cm under a purge, an anti-glare film (AGF−) that has been cured by irradiating ultraviolet rays with an irradiation amount of 130 mJ / cm ² 1) to (AGF-17) were prepared and wound up.

[Coating of low refractive index layer]
As for samples (AGF-2) to (AGF-17), a coating solution for low refractive index layer (LL-1) is further described on FIG. 1 of JP-A No. 2003-211052 on the antiglare layer. Using a slot die coater, wet coating was performed so that the dry film thickness of the low refractive index layer was 90 nm, drying at 60 ° C. for 50 seconds, and further purging with nitrogen purge to 240 W / cm under an atmosphere with an oxygen concentration of 100 ppm. Using an “air-cooled metal halide lamp” {manufactured by Eye Graphics Co., Ltd.}, irradiating with an ultraviolet ray having an irradiation amount of 400 mJ / cm ² , forming a low refractive index layer and winding it, and anti-glare film (AGF-2 ) To (AGF-17).

[Evaluation of anti-glare film]

[Evaluation of surface shape]
Arithmetic average roughness (Ra) and average interval of unevenness (Sm) were evaluated by the methods described in the text. Regarding Sm, the measurement length at the time of measurement was 8 mm, and the cut-off value was 0.8 mm.

[Inclination angle θ]
The inclination angle θ was measured by the method described in the text, and the frequency of the inclination angle 0 to 0.5 ° was calculated therefrom.

[Average particle size]
Using the electron microscope “S-3400N” {manufactured by Hitachi High-Technologies Corporation}, the produced antiglare film is photographed by transmission at a magnification of 5000 times. 100 photographed particles were randomly selected, and an average value of 100 particle diameters was defined as an average particle diameter.

[Average film thickness]
Using an electron microscope “S-3400N” {manufactured by Hitachi High-Technologies Corporation}, a cross section of the produced antiglare film is photographed at a magnification of 5000 times. Ten points of the film thickness of the antiglare layer are measured at random, and an average value is derived. This operation was performed for three fields of view, and the average value was defined as the average film thickness.

(Reflectance)
The back surface of the antireflection film was roughened with sandpaper and then treated with black ink to eliminate the back surface reflection. The surface of the antireflection film is attached to an integrating sphere of a spectrophotometer V-550 (manufactured by JASCO Corporation), and the reflectance (integrated reflectance) is measured in a wavelength region of 380 to 780 nm. An average reflectance of ˜650 nm was calculated, and antireflection properties were evaluated.

  Table 1 shows the layer structure of the obtained antiglare film and various measured properties.

<Preparation of polarizing plate C2>
Iodine was adsorbed on the stretched polyvinyl alcohol film to produce a polarizing film, the antiglare antireflection film AGF-2 was saponified, and attached to one side of the polarizing film using a polyvinyl alcohol adhesive. Further, a commercially available cellulose acylate film (Fujitac TD80UF, manufactured by Fuji Film Co., Ltd.) was subjected to saponification treatment on the other side of the polarizing film, and was bonded using a polyvinyl alcohol-based adhesive to produce a polarizing plate C2.

<Preparation of polarizing plates D1 to D17>
A polarizing film is produced by adsorbing iodine to a stretched polyvinyl alcohol film, anti-glare anti-reflection films AGF-1 to AGF-17 are saponified, and attached to one side of the polarizing film using a polyvinyl alcohol-based adhesive. I attached. Further, the polarizing plate protective film 1 was subjected to saponification treatment on the other side of the polarizing film and pasted using a polyvinyl alcohol-based adhesive to prepare polarizing plates D1 to D17.

<Preparation of polarizing plate E2>
Iodine was adsorbed on the stretched polyvinyl alcohol film to produce a polarizing film, the antiglare antireflection film AGF-2 was saponified, and attached to one side of the polarizing film using a polyvinyl alcohol adhesive. Further, the cellulose acylate film surface of the first retardation region 2 of the optical compensation film B prepared above is saponified on the other side of the polarizing film and pasted with a polyvinyl alcohol adhesive to produce a polarizing plate E2. did.

<Preparation of polarizing plate F2>
Iodine was adsorbed on the stretched polyvinyl alcohol film to produce a polarizing film, the antiglare antireflection film AGF-2 was saponified, and attached to one side of the polarizing film using a polyvinyl alcohol adhesive. Furthermore, the cellulose acylate film surface of the first retardation region 4 of the optical compensation film D prepared above is subjected to saponification treatment on the other side of the polarizing film and pasted with a polyvinyl alcohol adhesive to produce a polarizing plate F2. did.

The present invention will be described by taking as an example a liquid crystal display device including the first retardation region 1 created as described above, which satisfies the following condition (A) as the optical compensation region.
(A) 100 nm ≦ Re ≦ 400 nm and −50 nm ≦ Rth ≦ 50 nm

<Production of liquid crystal display device L1>
Using the acrylic pressure-sensitive adhesive on the polarizing plate protective film 1 side of the polarizing plate D1, the produced first retardation region 1 is arranged so that the absorption axis of the polarizing film and the slow axis of the first retardation region 1 are parallel to each other. Pasted on.

This is so that the absorption axis of the polarizing plate is parallel to the rubbing direction of the liquid crystal cell on the viewing side of the IPS mode liquid crystal cell 1 produced above (that is, the slow axis of the first retardation region 1 is black). It was pasted so that it was parallel to the slow axis of the liquid crystal molecules of the liquid crystal cell during display.
Subsequently, the polarizing plate A is pasted on the back side of the IPS mode liquid crystal cell 1 so that the polarizing plate protective film 1 side is on the liquid crystal cell side and the polarizing plate D1 is in a crossed Nicol arrangement, thereby displaying a liquid crystal display. Device L1 was made.
This configuration corresponds to the configuration shown in FIG. 6, and an antiglare layer is laminated on the first protective film side.

<Production of liquid crystal display devices L2 to L17>
The liquid crystal display devices L2 to L17 were created in the same manner as the liquid crystal display device L1 created above except that the viewing side polarizing plate D1 was replaced with the polarizing plates D2 to D17.

<Production of Liquid Crystal Display Device L18>
A liquid crystal display device L18 was produced in the same manner as the liquid crystal display device L1 produced above except that the viewing side polarizing plate D1 was replaced with the polarizing plate A.

<Production of liquid crystal display device L19>
A liquid crystal display device L19 was prepared in the same manner as in the liquid crystal display device L1 created above except that the viewing side polarizing plate D1 was replaced with the polarizing plate C2 and the back surface side polarizing plate A was replaced with the polarizing plate B.

<Production of liquid crystal display device L20>
For the liquid crystal display device L19 created above, the viewing side polarizing plate C2 is replaced with a polarizing plate C15 (in the above <Preparation of polarizing plate C2>, AGF-15 is used instead of AGF-2). Similarly, a liquid crystal display device L19 was produced.

  The liquid crystal display devices L1 to L13, which are examples of the present invention, and L14 to L19, which are comparative examples, were evaluated for oblique leakage light, bright room contrast, and reflection according to the following evaluation methods.

(1) Diagonal leakage light Place the liquid crystal cell 1 on the Schacus Ten set in the dark room without attaching the polarizing plate so that the substrate on which the electrode is disposed is on the Schaukasten side, and use the rubbing direction of the liquid crystal cell as a reference Luminance meter (spectral radiance meter CS-1000: manufactured by Minolta Co., Ltd.) installed at an angle of 45 degrees to the left and 1 m away from the normal direction of the liquid crystal cell at 60 degrees. 1 was measured.
Then, each liquid crystal display device having a polarizing plate bonded on the same Schaukasten as described above was placed, and the luminance 2 was measured in the same manner as described above.

(2) Bright room contrast Each liquid crystal display device in which a polarizing plate is bonded to a Schacusten set in a bright room is placed so that the substrate on which the electrode is disposed is on the Schacusten side, and the normal line of the liquid crystal cell. A contrast ratio, which is a luminance ratio (white display / black display), was measured with a luminance meter (spectral radiance meter CS-1000: manufactured by Minolta Co., Ltd.) installed at a distance of 1 m in the direction.

(3) on the viewer's side of the glare liquid crystal display device manufactured above reflects bare fluorescent lamp of (8000 cd / m ²⁾ from an angle of 45 degrees, the degree of blurring of the reflected image when observed from the direction of -45 degrees Was evaluated according to the following criteria.
I do not know the outline of the fluorescent lamp at all: ◎
Slightly understand the outline of the fluorescent lamp: ○
The fluorescent lamp is blurred, but the outline can be identified: △
Fluorescent lamp is hardly blurred: ×

From the results shown in Table 2, the following is clear.
The average particle diameter of the translucent particles is 0.01 to 4.0 μm larger than the average film thickness of the antiglare layer, and the translucent particles are 0.1 to 1 mass relative to the total solid content of the antiglare layer. The liquid crystal display device of the present invention having an antiglare layer of% is excellent with little oblique leakage light and no reflection.

Next, a liquid crystal display device corresponding to the second embodiment of the present invention, which includes a retardation region that satisfies at least one of the following conditions (B), (C), and (D) as an optical compensation region: The invention is illustrated by way of example.
(B) 60 nm ≦ Re ≦ 200 nm and 30 nm ≦ Rth ≦ 100 nm
(C) 0 nm ≦ Re ≦ 20 nm and −400 nm ≦ Rth ≦ −50 nm
(D) 30 nm ≦ Re ≦ 150 nm and 100 nm ≦ Rth ≦ 400 nm

<Production of liquid crystal display device L21>
Using the acrylic adhesive on the polarizing plate protective film 1 side of the polarizing plate D2, the optical compensation film B in which the first retardation region 2 and the second retardation region 1 are laminated is placed on the absorption axis of the polarizing film and the first position. The surface of the first phase difference region 2 was pasted so that the slow axis of the phase difference region 2 was orthogonal.

This is so that the absorption axis of the polarizing plate is perpendicular to the rubbing direction of the liquid crystal cell on the viewing side of the IPS mode liquid crystal cell 1 produced above (that is, the slow axis of the first retardation region 2 is black). It was pasted so that it was parallel to the slow axis of the liquid crystal molecules of the liquid crystal cell during display.
Subsequently, the polarizing plate A is pasted on the back side of the IPS mode liquid crystal cell 1 so that the polarizing plate protective film 1 side is on the liquid crystal cell side and the polarizing plate D2 is in a crossed Nicol arrangement, thereby displaying a liquid crystal display. Apparatus L21 was produced. The configuration of the liquid crystal display device 21 corresponds to the configuration shown in FIG. 8, and an antiglare layer is laminated on the first protective film 101. The first retardation region 2 of the optical compensation film B satisfies the condition (D), and the second retardation region 1 satisfies the condition (C).

<Production of liquid crystal display device L22>
Using the acrylic adhesive on the polarizing plate protective film 1 side of the polarizing plate D2, the optical compensation film C in which the first retardation region 3 and the second retardation region 2 are laminated is placed on the absorption axis of the polarizing film and the first position. The surface of the first phase difference region 3 was pasted so that the slow axis of the phase difference region 3 was orthogonal.
This is so that the absorption axis of the polarizing plate is parallel to the rubbing direction of the liquid crystal cell on the viewing side of the IPS mode liquid crystal cell 1 produced above (that is, the slow axis of the first retardation region 3 is black). It was pasted so that it was parallel to the slow axis of the liquid crystal molecules of the liquid crystal cell during display.
Subsequently, the polarizing plate A is pasted on the back side of the IPS mode liquid crystal cell 1 so that the polarizing plate protective film 1 side is on the liquid crystal cell side and in a crossed Nicol arrangement with the polarizing plate A. Apparatus L22 was produced. The configuration of the liquid crystal display device 22 corresponds to the configuration shown in FIG. 8, and an antiglare layer is laminated on the first protective film 101. The first retardation region 3 of the optical compensation film B satisfies the condition (B), and the second retardation region 2 satisfies the condition (C).

<Production of liquid crystal display device L23>
Using the acrylic adhesive on the polarizing plate protective film 1 side of the polarizing plate D2, the optical compensation film D in which the first retardation region 4 and the second retardation region 3 are laminated is placed on the absorption axis of the polarizing film and the first position. The surface of the first phase difference region 4 was pasted so that the slow axis of the phase difference region 4 was orthogonal.
This is so that the absorption axis of the polarizing plate is parallel to the rubbing direction of the liquid crystal cell on the viewing side of the IPS mode liquid crystal cell 1 produced above (that is, the slow axis of the first retardation region 4 is black). It was pasted so that it was parallel to the slow axis of the liquid crystal molecules of the liquid crystal cell during display.
Subsequently, the polarizing plate A is pasted on the back side of the IPS mode liquid crystal cell 1 so that the polarizing plate protective film 1 side is on the liquid crystal cell side and in a crossed Nicol arrangement with the polarizing plate A, and the liquid crystal display device L23 was produced. The configuration of the liquid crystal display device 23 corresponds to the configuration shown in FIG. 8, and an antiglare layer is laminated on the first protective film 101. The first retardation region 4 of the optical compensation film D satisfies the condition (B), and the second retardation region 3 satisfies the condition (C).

<Production of Liquid Crystal Display Device L24>
The polarizing plate E2 is on the viewing side of the IPS mode liquid crystal cell 1 so that the second retardation region 1 side is on the liquid crystal cell side, and the absorption axis of the polarizing plate E2 is the slow axis of the liquid crystal molecules of the liquid crystal cell during black display. And pasted so as to be orthogonal.
Subsequently, the polarizing plate A is pasted on the back side of the IPS mode liquid crystal cell 1 so that the polarizing plate protective film 1 side is on the liquid crystal cell side, and in a crossed Nicol arrangement with the polarizing plate E2. L24 was produced. The configuration of the liquid crystal display device 24 is a configuration in which the first polarizing film cell side protective film 104 is not provided in the configuration shown in FIG. An antiglare layer is laminated on the first protective film 101. Further, the first retardation region 2 of the optical compensation film B satisfies the condition (B), and the second retardation region 1 satisfies the condition (C).

<Production of liquid crystal display device L25>
The polarizing plate F2 is on the viewing side of the IPS mode liquid crystal cell 1, the second retardation region 3 side is on the liquid crystal cell side, and the absorption axis of the polarizing plate F2 is the slow axis of the liquid crystal molecules of the liquid crystal cell during black display. And pasted so as to be orthogonal.
Subsequently, the polarizing plate A is pasted on the back side of the IPS mode liquid crystal cell 1 so that the polarizing plate protective film 1 side is on the liquid crystal cell side and in a crossed Nicol arrangement with the polarizing plate F2, and the liquid crystal display device L25 was produced. The configuration of the liquid crystal display device 22 is a configuration in which the first polarizing film cell side protective film 104 is not provided in the configuration shown in FIG. An antiglare layer is laminated on the first protective film 101. The first retardation region 4 of the optical compensation film B satisfies the condition (B), and the second retardation region 3 satisfies the condition (C).

  The liquid crystal display devices L21 to L25, which are embodiments of the present invention, were evaluated for oblique leakage light, bright room contrast, and reflection according to the above-described evaluation methods in the same manner as L2, and are summarized in Table 3.

  (A + B) described in the column of the optical compensation region means that the phase difference region A and the phase difference region B are mounted in this order from the side near the cell side protective film of the viewing side polarizing plate. The X-th order Y means the X-th phase difference Y.

From the results shown in Table 3, the following is clear.
Even when the optical compensation region satisfies at least one of (B), (C), and (D), the average particle diameter of the translucent particles is larger than the average film thickness of the antiglare layer as in the case of having (A). In addition, the liquid crystal display device of the present invention mounted with an antiglare layer having a size of 0.01 to 3.0 μm and the translucent particles being 0.1 to 1% by mass with respect to the total solid content of the antiglare layer is oblique. There is little light leakage, high contrast in the bright room, no reflection, no brownish feeling, and excellent.
Further, the configuration (L24, L25) using a cellulose ester film in the first retardation region and excluding the polarizing plate protective film has less oblique light leakage than the configuration using the polarizing plate protective film, and the bright room contrast. Is high and good.

FIG. 1 is a schematic cross-sectional view schematically showing a preferred embodiment of the antiglare film of the present invention. FIG. 2 is a schematic cross-sectional view schematically showing an antiglare film in which a low refractive index layer is coated on a smooth surface. FIG. 3 is a schematic cross-sectional view schematically showing an antiglare film obtained by coating a low refractive index layer on the antiglare film. FIG. 4 is a schematic cross-sectional view schematically showing an antiglare film obtained by coating a low refractive index layer on the antiglare film. FIG. 5 is a schematic diagram showing an example of a pixel region of the liquid crystal display device of the present invention. FIG. 6 is a schematic view of the first embodiment of the liquid crystal display device of the present invention. FIG. 7 is a schematic diagram of the first embodiment of the liquid crystal display device of the present invention. FIG. 8 is a schematic view of a second embodiment of the liquid crystal display device of the present invention. FIG. 9 is a schematic view of a second embodiment of the liquid crystal display device of the present invention. FIGS. 10A to 10C are schematic diagrams for explaining the outline of the method of measuring the tilt angle.

Explanation of symbols

(1): Transparent support (2): Antiglare layer (5): Low refractive index layer 11: Transparent support 21: Smooth layer 22: Antiglare layer 23: Antiglare layer 51: Low refractive index layer 101: No. 1 protective film (first polarizing film outer protective film)
102: First polarizing film absorption axis direction 103: First polarizing film 104: First polarizing film cell side protective film 105: Slow axis direction of liquid crystal cell during black display 106: Liquid crystal cell 107: Second polarizing film cell side Protective film 108: second polarizing film 109: second polarizing film absorption axis direction 110: second protective film (second polarizing film outer protective film)
111: first phase difference region 112: slow axis direction of the first phase difference region 113: second phase difference region 201: liquid crystal element pixel region 202: pixel electrode 203: display electrode 204: rubbing direction 205a, 205b: black display Liquid crystal compound directors 206a and 206b: Liquid crystal compound directors for white display

Claims (17)

At least a first protective film, a first polarizing film, an optical compensation region, a liquid crystal cell having a liquid crystal layer and a pair of substrates sandwiching the liquid crystal layer, a second polarizing film, and a second protective film A liquid crystal display device in which the liquid crystal molecules of the liquid crystal layer are aligned in parallel to the surfaces of the pair of substrates at the time of black display, and at least one of the first protective film and the second protective film Has an antiglare layer,
Of the antiglare layer,
The center line average roughness (Ra) is 0.03 μm <Ra <0.4 μm,
The average interval (Sm) of the irregularities is 80 μm <Sm <700 μm,
A liquid crystal display device in which an area of 0 ° <θ <0.5 ° (θ (0.5)) occupies 40% to 98% at an inclination angle θ of the unevenness.   The said glare-proof layer contains at least 1 sort (s) of translucent particle | grains, The average particle diameter of this translucent particle | grain is 0.01-4.0 micrometers larger than the average film thickness of the said glare-proof layer. Liquid crystal display device.   3. The liquid crystal display device according to claim 1, wherein an addition amount of the translucent particles is 0.01 to 1% by mass with respect to a total solid content of the antiglare layer.   The liquid crystal display device according to claim 1, wherein the translucent particles have an average particle size of 3 μm to 15 μm.   The liquid crystal display device according to any one of claims 1 to 4, further comprising a low refractive index layer having a refractive index lower than that of the antiglare layer on a surface of the antiglare layer. The liquid crystal display device according to claim 1, wherein the optical compensation region includes at least one retardation region that satisfies any of the following formulas (A) to (D).
(A) 100 nm ≦ Re ≦ 400 nm and −50 nm ≦ Rth ≦ 50 nm
(B) 60 nm ≦ Re ≦ 200 nm and 30 nm ≦ Rth ≦ 100 nm
(C) 0 nm ≦ Re ≦ 20 nm and −400 nm ≦ Rth ≦ −50 nm
(D) 30 nm ≦ Re ≦ 150 nm and 100 nm ≦ Rth ≦ 400 nm
(Here, Re is in-plane retardation, and Rth is retardation in the thickness direction.)   The liquid crystal display device according to claim 6, wherein the first retardation region satisfying any one of the formulas (A) to (D) is a cellulose ester film.   8. The liquid crystal display device according to claim 6, wherein the optical compensation region includes a first retardation region that satisfies the formula (A), and a value Nz of the first retardation region is 0.45 to 0.55. . The optical compensation region includes a first retardation region and a second retardation region;
The in-plane retardation Re of the first retardation region is 60 nm to 200 nm,
The thickness direction retardation Rth of the first retardation region is 30 nm to 100 nm,
In-plane retardation Re of the second retardation region is 0 nm to 20 nm,
The liquid crystal display device according to claim 1, wherein a retardation Rth in the thickness direction of the second retardation region is −300 nm to −100 nm.   The first polarizing film, the first retardation region, the second retardation region, and the liquid crystal cell are provided in this order, and the slow axis of the first retardation region is that of the first polarizing film. The liquid crystal display device according to claim 9, which is substantially orthogonal to the absorption axis.   The first polarizing film, the second retardation region, the first retardation region, and the liquid crystal cell are provided in this order, and the slow axis of the first retardation region is that of the first polarizing film. The liquid crystal display device according to claim 9, which is substantially parallel to the absorption axis. The optical compensation region includes a first retardation region and a second retardation region;
The in-plane retardation Re of the first retardation region is 30 nm to 150 nm,
The thickness direction retardation Rth of the first retardation region is 100 nm to 400 nm,
In-plane retardation Re of the second retardation region is 0 nm to 20 nm,
2. The retardation Rth in the thickness direction of the second retardation region is −400 nm to −80 nm, and the absorption axis of the first polarizing film is perpendicular to the slow axis direction of liquid crystal molecules during black display. The liquid crystal display device according to any one of?   The first polarizing film, the first retardation region, the second retardation region, and the liquid crystal cell are provided in this order, and the slow axis of the first retardation region is that of the first polarizing film. The liquid crystal display device according to claim 12, which is substantially perpendicular to the absorption axis.   The first polarizing film, the second retardation region, the first retardation region, and the liquid crystal cell are provided in this order, and the slow axis of the first retardation region is that of the first polarizing film. The liquid crystal display device according to claim 12, which is substantially parallel to the absorption axis.   The liquid crystal display device according to claim 9, wherein the second retardation region has a retardation layer containing a rod-like liquid crystal compound that is substantially vertically aligned.   The liquid crystal display device according to claim 1, further comprising a protective film between the second polarizing film and the substrate, wherein the retardation Rth in the thickness direction of the protective film is −50 nm to 40 nm. .   The liquid crystal display according to claim 1, further comprising a protective film between the second polarizing film and the substrate, wherein the protective film is a cellulose acylate film, a norbornene film, or an acrylic film. apparatus.