JP2016136259A - Liquid crystal display device - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a liquid crystal display device exhibiting a high front contrast and suppressing display unevenness.SOLUTION: A liquid crystal cell 20 include: an array substrate 100 disposed on a side close to a second polarizing plate 60 and having a thin film transistor and a color filter 230 disposed thereon; a counter substrate 200 disposed on a side close to a first polarizing plate 40 and opposing to the array substrate 100; and a liquid crystal layer 300 comprising liquid crystal molecules and held between the array substrate 100 and the counter substrate 200. The second polarizing plate 60 includes a second polarizer 62 and a protective film 64(F3) disposed between the second polarizer 62 and the array substrate 100. The protective film 64 (F3) includes a transparent polymer base layer and a resin layer disposed on a surface of the transparent polymer base layer, the surface on a side close to the second polarizer 62, and comprising a thermoplastic resin containing a polyether unit, a polyester unit or a polyacrylic unit. An adhesive layer comprising a cured product of a photocurable resin is disposed between the resin layer and the second polarizer 62.SELECTED DRAWING: Figure 1

Description

  The present invention relates to a liquid crystal display device.

  The liquid crystal display device is advantageous in that it is thinner and lighter than CRT (Cathode Ray Tube) and has low power consumption. Therefore, various electronic devices such as a television, a PC (personal computer), a PDA (mobile terminal), and a mobile phone are used. Widely used in equipment.

  In particular, VA (Vertical Alignment) type liquid crystal display devices are widely used for television applications because they have better viewing angle characteristics than conventional TN (Twisted Nematic) type liquid crystal display devices.

  VA liquid crystal display devices are required to further increase front contrast and reduce power consumption. On the other hand, as a liquid crystal display device having a high aperture ratio, a liquid crystal display device having a light-shielding portion (black matrix) minimized and a color filter on array (hereinafter abbreviated as “COA”) structure. Has been proposed (see Patent Document 1). In addition, the VA type includes a liquid crystal layer including a liquid crystal having positive dielectric anisotropy and a pair of substrates sandwiching the liquid crystal layer, and an electrode for driving the liquid crystal is provided on only one of the pair of substrates. A liquid crystal display device having a liquid crystal cell has also been proposed (see, for example, Patent Document 2).

  In addition, it is known that a liquid crystal display device causes display unevenness due to a dimensional change of a polarizing plate due to humidity and heat and a warp of a liquid crystal cell due to the change. In order to reduce such display unevenness, a retardation film in which the tensile elastic modulus and optical characteristics are adjusted (see Patent Document 3), and a retardation film in which the photoelastic modulus and optical characteristics are adjusted (Patent Document 4). Have been proposed). In addition, a polarizing plate has been proposed that includes a transparent substrate film, an easy-adhesion layer, an adhesive layer containing a photocurable resin, and a polarizer in this order (see Patent Document 5 and the like). Furthermore, a polarizing plate (see Patent Document 6) having a predetermined layer configuration and suppressing warpage, and a polarizing plate (see Patent Document 7) in which the moisture content is adjusted have been proposed.

JP 2008-146004 A JP 2009-301010 A JP 2008-217021 A JP 2011-95401 A JP 2009-98623 A JP 2010-217844 A JP 2010-243858 A

  However, a liquid crystal display device with a high aperture ratio has a problem that display unevenness that has not been recognized in the past is easily noticeable because the amount of transmitted light is large.

  The main factors causing display unevenness are considered to be 1) uneven adhesion between the polarizer and the protective film, and 2) warpage of the liquid crystal panel. 1) It is considered that uneven adhesion between the polarizer and the protective film is caused by surface treatment such as corona treatment or saponification treatment applied to the protective film. 2) It is considered that the warpage of the liquid crystal panel occurs when the polarizing plate sandwiching the liquid crystal cell undergoes a dimensional change under an environment in which humidity and heat fluctuate; In particular, in a liquid crystal cell having a COA structure, members such as a color filter and a thin film transistor are arranged so as to be biased to one of a pair of substrates. Therefore, the warp of the liquid crystal panel is more likely to occur due to the force of changing the size of the polarizing plate, and there is a problem that display unevenness is more conspicuous.

  The films and polarizing plates described in Patent Documents 3 to 7 have not been studied for use in liquid crystal display devices having a high aperture ratio as described above.

  The present invention has been made in view of the above circumstances, and an object of the present invention is to provide a liquid crystal display device having high front contrast and suppressed display unevenness.

[1] A liquid crystal display device having a first polarizing plate, a liquid crystal cell, a second polarizing plate, and a backlight in this order, wherein the liquid crystal cell is disposed on the second polarizing plate side. , An array substrate provided with a thin film transistor and a color filter, a counter substrate disposed on the first polarizing plate side and facing the array substrate, and sandwiched between the array substrate and the counter substrate, A liquid crystal layer including liquid crystal molecules, and the second polarizing plate includes a second polarizer and a protective film F3 disposed between the second polarizer and the array substrate. The protective film F3 is a thermoplastic resin that is disposed on a surface of the transparent polymer substrate layer and the second polarizer side of the transparent polymer substrate layer, and includes a polyether unit, a polyester unit, or a polyacryl unit. Tree containing A liquid crystal display device comprising an oil layer, wherein an adhesive layer containing a cured product of a photocurable resin is disposed between the resin layer of the protective film F3 and the second polarizer.
[2] The first polarizing plate has a first polarizer and a protective film F2 disposed between the first polarizer and the counter substrate, and the protective film F2 is transparent. A polymer substrate layer, and a resin layer that is disposed on a surface of the transparent polymer substrate layer on the first polarizer side and includes a thermoplastic resin including a polyether unit, a polyester unit, or a polyacryl unit, The liquid crystal display device according to [1], wherein an adhesive layer including a cured product of a photocurable resin is disposed between the resin layer of the protective film F2 and the first polarizer.
[3] The second polarizing plate further includes a protective film F4 disposed on a backlight side surface of the second polarizing plate, and the protective film F4 includes a transparent polymer base material layer and the transparent film. A resin layer including a thermoplastic resin including a polyether unit, a polyester unit, or a polyacrylic unit, disposed on a surface of the polymer substrate layer on the second polarizer side, and the resin layer of the protective film F4 The liquid crystal display device according to [1] or [2], wherein an adhesive layer including a cured product of a photocurable resin is disposed between the first polarizer and the second polarizer.
[4] The liquid crystal display device according to [1], wherein the transparent polymer base material layer includes cyclic polyolefin or (meth) acrylic resin.
[5] The liquid crystal display device according to [1] or [4], wherein the thermoplastic resin included in the resin layer is a urethane resin.
[6] The liquid crystal display device according to any one of [1] and [4] to [5], wherein the resin layer further includes fine particles.
[7] The liquid crystal display device according to any one of [1] and [4] to [6], wherein the photocurable resin included in the adhesive layer is an ultraviolet curable resin.
[8] The liquid crystal display device according to any one of [1] and [4] to [7], wherein the photocurable resin contained in the adhesive layer is a (meth) acrylamide resin or an epoxy resin.
[9] The liquid crystal display device according to any one of [1] and [4] to [8], wherein the transparent polymer base material layer has a thickness of 20 to 40 μm.
[10] The liquid crystal display device according to any one of [1] and [4] to [9], wherein the aperture ratio is 65% or more.
[11] The liquid crystal cell aligns the liquid crystal molecules perpendicularly to the surface of the array substrate when no voltage is applied, and aligns the liquid crystal molecules horizontally with respect to the surface of the array substrate when a voltage is applied. The liquid crystal display device according to any one of [1] to [10].
[12] The liquid crystal molecules are liquid crystal molecules having positive dielectric anisotropy, and the array substrate has a pixel electrode and a counter electrode that drive the liquid crystal molecules. [1] to [11] A liquid crystal display device according to any one of the above.
[13] The liquid crystal display device according to any one of [1] to [12], wherein the liquid crystal cell is an FFS (Fringe Field Switching) driving method.
[14] The liquid crystal display device according to any one of [1] to [13], wherein the backlight is an LED backlight.

  The liquid crystal display device of the present invention has a high front contrast and can suppress display unevenness.

It is a schematic diagram which shows the basic composition of one Embodiment of the liquid crystal display device which concerns on this invention. It is a lamination sectional view of a liquid crystal cell which has a COA structure. FIG. 3 is a top view of an array substrate of a liquid crystal cell having the COA structure of FIG. 2. It is a schematic diagram which shows an example of the mode of the display nonuniformity when a display screen is displayed in black.

1. Liquid Crystal Display Device The liquid crystal display device of the present invention includes a liquid crystal cell, a pair of polarizing plates that sandwich the liquid crystal cell, and a backlight.

  FIG. 1 is a schematic diagram showing a basic configuration of an embodiment of a liquid crystal display device according to the present invention. As shown in FIG. 1, the liquid crystal display device 10 includes a liquid crystal cell 20, a first polarizing plate 40 and a second polarizing plate 60 that sandwich the liquid crystal cell 20, and a backlight 80.

About the liquid crystal cell 20 Examples of the display method of the liquid crystal cell 20 include a TN (Twisted Nematic) method, an STN (Super Twisted Nematic) method, a HAN (Hybrid Alignment Nematic) method, an IPS (In-Plane Switching) method, an VA (In Plane Switching) metric method, and a VA (In Plane Switching) method. ) Method, MVA (Multiple Vertical Alignment) method, OCB (Optical Compensated Bend) method, and the like. Among them, the VA method and the MVA method (vertical alignment type liquid crystal cell) are preferable because of high contrast.

  The liquid crystal cell 20 includes an array substrate 100, a counter substrate 200 facing the array substrate 100, and a liquid crystal layer 300 sandwiched between the array substrate 100 and the counter substrate 200.

  The array substrate 100 includes an insulating substrate 110, a thin film transistor (not shown) disposed thereon, a color filter 230, and a pixel electrode (not shown). The counter substrate 200 has an insulating substrate 210. The counter electrode may be provided on the insulating substrate 210 or may be provided on the insulating substrate 110. Specific examples of the liquid crystal cell having a COA structure include those described in JP-A-10-206888.

  The liquid crystal layer 300 is not particularly limited, but is preferably a VA mode (vertical alignment type) liquid crystal layer and includes liquid crystal molecules 31. The liquid crystal molecules contained in the liquid crystal layer are liquid crystal molecules having negative or positive dielectric anisotropy.

  In order to increase the aperture ratio of the liquid crystal cell, it is preferable that both the pixel electrode and the counter electrode are disposed on the insulating substrate 110, and the liquid crystal molecules are liquid crystal molecules having positive dielectric anisotropy.

  Examples of liquid crystal molecules having negative dielectric anisotropy include nematic liquid crystal molecules having negative dielectric anisotropy. Examples of nematic liquid crystal molecules having negative dielectric anisotropy include those described in JP-A No. 2004-204133, JP-A No. 2004-250668, JP-A No. 2005-047980, and the like. Specifically, a nematic liquid crystal material having negative dielectric anisotropy and about Δn = 0.0815 and Δε = −4.5 is preferably used.

  Examples of liquid crystal molecules having positive dielectric anisotropy include nematic liquid crystal molecules having positive dielectric anisotropy. As an example of nematic liquid crystal molecules having positive dielectric anisotropy, liquid crystal materials used in TN type and IPS type liquid crystal display devices can be used. Specifically, a nematic liquid crystal material having positive dielectric anisotropy and having Δn = 0.0815 and Δε = 4.5 is preferably used.

  The liquid crystal layer 300 may include a chiral material that is included in a TN liquid crystal cell as necessary in order to reduce alignment defects of liquid crystal molecules.

  The thickness of the liquid crystal layer 300 is not particularly limited, but may be about 3.5 μm, for example, when the above-described nematic liquid crystal material having negative or positive dielectric anisotropy is used.

  The liquid crystal cell 20 may have a multi-domain structure. A multi-domain structure refers to a structure in which one pixel of a liquid crystal cell is divided into a plurality of regions. In a liquid crystal cell having a multi-domain structure, the alignment of liquid crystal molecules in the boundary region between the domains can be adjusted. For example, in a VA liquid crystal cell, liquid crystal molecules are inclined during white display. Therefore, in a VA liquid crystal cell that does not have a multi-domain structure, a difference in luminance and color tone tends to occur because the birefringence of liquid crystal molecules differs between the tilt direction and the opposite direction. On the other hand, a VA liquid crystal cell having a multi-domain structure is preferable because the viewing angle characteristics of luminance and color tone are improved.

  Specifically, a liquid crystal cell having a multi-domain structure may have two or more regions in which the initial alignment state of liquid crystal molecules is different from each other for each pixel. As a result, the liquid crystal cell having a multi-domain structure is less biased in birefringence as a whole of the liquid crystal cell, so that the bias in luminance and color tone depending on the viewing angle can be reduced. A liquid crystal cell having a multi-domain structure can also obtain the same effect by having two or more regions in which the orientation directions of liquid crystal molecules that continuously change in a voltage applied state are different from each other in each pixel. . In order to obtain a uniform viewing angle in all directions, the number of divisions for each pixel may be increased, and if the number of divisions is four or more or eight or more, a substantially uniform viewing angle can be obtained in all directions. In particular, when it is divided into eight, the absorption axis of the polarizing plate can be set to an arbitrary angle, which is preferable.

  The liquid crystal cell 20 is preferably an FFS (Fringe Field Switching) driving method from the viewpoint of increasing the aperture ratio of the display device. An FFS driving type liquid crystal cell includes a common electrode provided in a planar shape and a stripe-shaped pixel electrode provided so as to overlap the common electrode. The liquid crystal molecules are driven not only by the electric field generated between the pixel electrode and the counter electrode but also by the electric field generated between the pixel electrode and the common electrode. Specific examples of the FS type VA liquid crystal cell include those described in paragraphs 0094 to 0107 of JP-A-2009-301010.

  2 and 3 are schematic views showing an example of a preferred configuration of a liquid crystal cell having a COA structure. FIG. 2 is a cross-sectional view of a liquid crystal cell having a COA structure. FIG. 3 is a top view of an array substrate 100 (see FIG. 2) of a liquid crystal cell having a COA structure. 2 is a cross-sectional view taken along line XVI-XVI in FIG.

  As shown in FIG. 2, the liquid crystal cell 20 includes an array substrate 100, a counter substrate 200 facing the array substrate 100, and a liquid crystal layer 300 sandwiched therebetween.

  As shown in FIGS. 2 and 3, the array substrate 100 includes a common electrode 270, a pixel electrode 191 a (pixel electrode), and a pixel electrode 191 b (counter electrode) with the insulating substrate 110 as a substrate. . The pixel electrodes 191 a and the pixel electrodes 191 b are alternately arranged in a stripe pattern on the insulating substrate 110. The common electrode 270 is disposed in a planar shape on the insulating substrate 110. Then, the pixel electrode 191a and the pixel electrode 191b overlap with the common electrode 270 (see FIG. 3).

  The insulating substrate 110 is a transparent substrate and is made of transparent glass or resin.

  As shown in FIG. 2, the array substrate 100 includes an insulating substrate 110, a thin film transistor, a pixel electrode 191a, and a pixel electrode 191b. The pixel electrode 191a is connected to the drain electrode 175a of the thin film transistor. Similarly, the pixel electrode 191b is connected to the drain electrode 175b of the thin film transistor (not shown in FIG. 2). As shown in FIG. 3, the thin film transistor connected to each pixel electrode is disposed at the corner of each pixel.

  As shown in FIG. 2, the thin film transistor includes a gate electrode 124a, a gate insulating film 140, an island-shaped semiconductor 154a, first and second island-shaped ohmic contact members (163a and 165a), and a source electrode 173a. And a drain electrode 175a. The source electrodes (173a, 173b) are connected to data lines (171a, 171b) for transmitting data signals, respectively (see FIG. 3).

  The thin film transistor is covered with a lower protective film 180p, and a light shielding member 220 or a color filter 230 is disposed on the lower protective film 180p. The light shielding member 220 or the color filter 230 is further covered with the upper protective film 180q, and the pixel electrode 191a is disposed on a part of the upper protective film 180q. The pixel electrode 191a is connected to the drain electrode 175a through a contact hole 185a provided in the lower protective film 180p and the upper protective film 180q. Further, the upper protective film 180q and the pixel electrode 191a are covered with the alignment film 11. Reference numeral 225 a is a through hole, and reference numeral 227 is an opening of the light shielding member 220.

  In the counter substrate 200, the insulating substrate 210 and the alignment film 21 are stacked in this order. The insulating substrate 210 is made of transparent glass or resin, like the insulating substrate 110 described above.

  The liquid crystal molecules 31 included in the liquid crystal layer 300 are preferably a nematic liquid crystal material (p-type nematic liquid crystal material) having positive dielectric anisotropy.

  In the liquid crystal cell 20 configured as described above, when a common voltage is applied to the common electrode 270 and data voltages having different polarities are applied to the pixel electrodes (191a, 191b), the surface of the array substrate 100 or the counter substrate 200 is applied. An almost horizontal electric field is generated. As a result, the liquid crystal molecules 31 that are vertically aligned with respect to the surface of the array substrate 100 or the counter substrate 200 when no voltage is applied respond to the electric field, and the major axis thereof is relative to the surface of the array substrate 100 or the counter substrate 200. Oriented in the horizontal direction. Thereby, an image can be displayed on the display screen of the liquid crystal display device.

  Furthermore, in addition to the electric field generated between the pixel electrode 191a and the pixel electrode 191b, an electric field generated between the pixel electrode 191a and the common electrode 270 or between the pixel electrode 191b and the common electrode 270 also The liquid crystal molecules 31 can be aligned (FFS drive can be performed). Therefore, the viewing angle can be widened and the transmittance can be increased.

  The liquid crystal cell 20 configured in this manner has a high aperture ratio because wiring lines such as gate lines and data lines are reduced. The aperture ratio of the liquid crystal display device is preferably 57% or more, and more preferably 65% or more.

  The first polarizing plate 40 is disposed on the viewing side surface of the liquid crystal cell 20 (see FIG. 1), and includes a first polarizer 42 and protective films 44 (F1) and 46 (F2) sandwiching the first polarizer 42. Have. On the other hand, the 2nd polarizing plate 60 is arrange | positioned at the backlight side of the liquid crystal cell 20, and has the 2nd polarizer 62 and the protective films 64 (F3) and 66 (F4) which clamp it. The protective film 46 (F2) may be omitted as necessary.

  When the liquid crystal cell 20 is a VA system, it arrange | positions so that the in-plane slow axis of the protective film 46 (F2) and the absorption axis of the 1st polarizer 42 may orthogonally cross. Similarly, it arrange | positions so that the in-plane slow axis of the protective film 64 (F3) and the absorption axis of the 2nd polarizer 62 may orthogonally cross.

  As described above, a liquid crystal display device with a high aperture ratio has a large amount of transmitted light, and thus display unevenness that has not been recognized in the past is easily noticeable. FIG. 4 is a schematic diagram illustrating an example of display unevenness when the display screen is displayed in black. As shown in FIG. 4, for example, display unevenness when black is displayed can be confirmed as white portions (light leakage) generated at the four corners of the display screen. Such display unevenness in a liquid crystal display device having a COA structure is mainly caused by 1) uneven adhesion between a protective film and a polarizer, and 2) a liquid crystal cell structure having high asymmetry such as a COA structure. Was found.

  The surface of the protective film to be bonded to the polarizer of 1) is usually subjected to a surface treatment such as saponification treatment, corona treatment or plasma treatment in order to enhance the adhesion to the polarizer. However, when the protective film is surface-treated, foreign matter is generated, and the foreign matter repels the adhesive and tends to cause poor adhesion with the polarizer. In addition, unevenness is likely to occur in the surface treatment itself, and thereby, the retardation unevenness and the axial alignment unevenness of the protective film are also likely to occur.

  In the liquid crystal cell having the COA structure of 2), the thin film transistor and the color filter are arranged so as to be biased toward one of the pair of substrates. Thus, since the liquid crystal cell having a COA structure has a highly asymmetric structure, the liquid crystal cell is likely to warp due to the force of changing the size of the polarizing plate. The warpage of the liquid crystal cell occurs so that the central portion is convex toward the backlight side; specifically, it tends to occur so that the array substrate side is the outer peripheral side and the counter substrate side is the inner peripheral side.

  Therefore, in the present invention, in order to reduce display unevenness, at least the protective film F3 is a protective film having a configuration that eliminates the need for surface treatment; that is, “transparent polymer base layer, polyether unit, polyester unit, or polyacrylic” It is referred to as a “protective film having a resin layer (specific resin layer) containing a thermoplastic resin containing unit” (protective film having a specific resin layer). Further, in order to further improve the adhesive property of the polarizer and reduce the warpage of the liquid crystal cell, at least the “adhesion including a cured product of a photocurable resin” is provided between the specific resin layer of the protective film F3 and the polarizer. Layer ".

  That is, at least the protective film F3; preferably both the protective films F3 and F2; more preferably all of the protective films F2, F3 and F4 are “protective films having a specific resin layer”; and a specific resin of the protective film A “adhesive layer containing a cured product of a photocurable resin” is disposed between the layer and the polarizer.

  Hereinafter, at least the “protective film having a specific resin layer” used for the protective film F3 will be described. The protective film which has a specific resin layer has a transparent polymer base material layer and a specific resin layer.

About a transparent polymer base material layer A transparent polymer base material layer contains a thermoplastic resin. Examples of the thermoplastic resin contained in the transparent polymer base layer include cellulose ester, polyethylene (PE), high density polyethylene, medium density polyethylene, low density polyethylene, polypropylene (PP), polyvinyl chloride (PVC), polychlorinated Vinylidene, polystyrene (PS), polyvinyl acetate (PVAc), Teflon (registered trademark) (polytetrafluoroethylene, PTFE), ABS resin (acrylonitrile butadiene styrene resin), AS resin, (meth) acrylic resin (PMMA), etc. included.

  From the viewpoint of increasing mechanical strength and breaking strength, polyamide (PA), nylon, polyacetal (POM), polycarbonate (PC), modified polyphenylene ether (m-PPE, modified PPE, PPO), polybutylene terephthalate (PBT), Thermoplastic resins such as polyethylene terephthalate (PET), glass fiber reinforced polyethylene terephthalate (GF-PET), and cyclic polyolefin (COP) can also be used.

  From the viewpoint of improving heat resistance and durability, polyphenylene sulfide (PPS), polytetrafluoroethylene (PTFE), polysulfone, polyethersulfone, amorphous polyarylate, liquid crystal polymer, polyetheretherketone, thermoplastic polyimide ( Thermoplastic resins such as PI) and polyamideimide (PAI) can also be used.

  Among these, cellulose ester, cyclic polyolefin or (meth) acrylic resin is preferable, and cyclic polyolefin or (meth) acrylic resin is more preferable because of low moisture permeability.

Cellulose ester Cellulose ester is a compound obtained by esterifying a hydroxyl group of cellulose with an aliphatic carboxylic acid or an aromatic carboxylic acid.

  The acyl group contained in the cellulose ester is an aliphatic acyl group or an aromatic acyl group, preferably an aliphatic acyl group. Examples of the aliphatic acyl group include acetyl group, propionyl group, butanoyl group, heptanoyl group, hexanoyl group, octanoyl group, decanoyl group, dodecanoyl group, tridecanoyl group, tetradecanoyl group, hexadecanoyl group, octadecanoyl group , Isobutanoyl group, tert-butanoyl group, cyclohexanecarbonyl group, oleoyl group, cinnamoyl group, etc., preferably acetyl group, propionyl group, butanoyl group, dodecanoyl group, octadecanoyl group, tert-butanoyl group, oleoyl Group, a cinnamoyl group. Examples of the aromatic acyl group include a benzoyl group and a naphthylcarbonyl group. Of these, an aliphatic acyl group having 2 to 4 carbon atoms such as an acetyl group, a propionyl group, and a butanoyl group is preferable, and an acetyl group is particularly preferable.

  The acyl group substitution degree of the cellulose ester is preferably 2.00 to 2.75, and more preferably 2.25 to 2.50. This is because a film containing a cellulose ester has an appropriate retardation and can have good transparency and wavelength dispersion. The acyl group substitution degree can be adjusted by reaction conditions (time, temperature, sample concentration, etc.) when esterifying cellulose.

  The acyl group substitution degree refers to the total of the ratios of esterification of hydroxyl groups (hydroxyl groups) at the 2nd, 3rd and 6th positions of glucose which is a repeating unit of cellulose constituting the cellulose ester. For example, when all the hydroxyl groups at the 2-position, 3-position and 6-position of cellulose are each 100% esterified, the degree of acyl group substitution is 3 at the maximum. The measuring method of acyl group substitution degree can be measured according to ASTM-D817-96.

  The cellulose ester is preferably at least one selected from cellulose (di, tri) acetate, cellulose propionate, cellulose butyrate, cellulose acetate propionate, cellulose acetate butyrate, cellulose acetate phthalate, and cellulose phthalate. Of these, cellulose triacetate, cellulose propionate, cellulose butyrate, cellulose acetate propionate, cellulose acetate butyrate and the like are preferable.

The cellulose ester preferably satisfies the following formulas (I) and (II) at the same time when the substitution degree of the acetyl group is X and the substitution degree of the propionyl group or butyryl group is Y.
Formula (I) 1.5 ≦ X + Y ≦ 3.0
Formula (II) 0 ≦ X ≦ 2.5

  The molecular weight distribution (weight average molecular weight Mw / number average molecular weight Mn) of the cellulose ester is preferably 1.5 to 5.5, more preferably 2.0 to 5.0, and more preferably 2.5 to 5. 0.0 is more preferable, and 3.0 to 5.0 is particularly preferable.

  1 g of cellulose ester is added to 20 ml of pure water (electric conductivity 0.1 μS / cm or less, pH 6.8), and the pH of the solution obtained by stirring in a nitrogen atmosphere at 25 ° C. for 1 hr is 6-7. It is preferable that the electric conductivity is 1 to 100 μS / cm.

  Cellulose esters can be synthesized by known methods. Specifically, cellulose is esterified in the presence of a catalyst (such as sulfuric acid) with a C3 or higher organic acid containing at least acetic acid or an anhydride thereof or an anhydride thereof to obtain a cellulose triester. Synthesize. In cellulose triesters, hydrogen atoms of three hydroxyl groups (hydroxyl groups) contained in the glucose unit are substituted with acyl groups derived from organic acids. Subsequently, the cellulose triester is hydrolyzed to synthesize a cellulose ester having a desired degree of acyl substitution. The obtained cellulose ester can be filtered, precipitated, washed with water, dehydrated and dried to obtain a cellulose ester (see the method described in JP-A-10-45804).

  Examples of cellulose used as a raw material include cotton linter, wood pulp (derived from conifers and hardwoods), kenaf and the like. The cellulose used as a raw material may be only one type or a mixture of two or more types.

(Meth) acrylic resin The (meth) acrylic resin that can be contained in the transparent polymer substrate layer is preferably a copolymer of methyl methacrylate and a monomer copolymerizable therewith. The content ratio of the structural units derived from methyl methacrylate in the copolymer is preferably 50 to 99% by mass.

  Examples of other copolymerizable monomers include alkyl methacrylates having 2 to 18 carbon atoms in the alkyl moiety; alkyl acrylates having 1 to 18 carbon atoms in the alkyl moiety; α, β such as acrylic acid and methacrylic acid -Unsaturated acid; unsaturated group-containing dicarboxylic acid such as maleic acid, fumaric acid and itaconic acid; aromatic vinyl compound such as styrene, α-methylstyrene and nucleus-substituted styrene; α, such as acrylonitrile and methacrylonitrile; β-unsaturated nitrile; maleic anhydride, maleimide, N-substituted maleimide, glutaric anhydride and the like are included. One type of copolymerizable monomer may be used, or two or more types may be used.

  Of these, methyl acrylate, ethyl acrylate, n-propyl acrylate, n-butyl acrylate, s-butyl acrylate, 2-ethylhexyl acrylate and the like are preferable, and methyl acrylate and n-butyl acrylate are more preferable.

  The (meth) acrylic resin may be a (meth) acrylic resin having a lactone ring structure from the viewpoint of enhancing the heat resistance and transparency of the resulting transparent polymer substrate layer and enhancing the mechanical strength. Examples of the (meth) acrylic resin having a lactone ring structure include JP 2000-230016, JP 2001-151814, JP 2002-120326, JP 2002-254544, JP 2005-146084, and the like. Includes those described in.

  Examples of commercially available (meth) acrylic resins include Delpet 60N, 80N (Asahi Kasei Chemicals Corporation), Dialnal BR52, BR80, BR83, BR85, BR88 (Mitsubishi Rayon Co., Ltd.), KT75 (Electricity). Chemical Industry Co., Ltd.).

Cyclic polyolefin Examples of cyclic olefin resins include norbornene resins, monocyclic olefin resins, cyclic conjugated diene resins, vinyl alicyclic hydrocarbon resins, hydrides thereof, and the like. Among these, norbornene-based resins are preferable because they are easy to mold and the resulting film has high transparency.

  Examples of the norbornene-based resin include a ring-opening polymer of a monomer having a norbornene structure, a ring-opening copolymer of a monomer having a norbornene structure and another monomer, or a hydride thereof, a norbornene structure The addition polymer of the monomer which has this, the addition copolymer of the monomer which has a norbornene structure, and another monomer, those hydrides, etc. are contained. Among them, it is easy to mold, and from the viewpoint of transparency, heat resistance, low hygroscopicity, dimensional stability, lightness, etc. of the resulting film, a ring-opening polymer or copolymer of a monomer having a norbornene structure or the like. The hydride is particularly preferred.

  Examples of the monomer having a norbornene structure include bicyclo [2.2.1] hept-2-ene (common name: norbornene), tricyclo [4.3.0.12,5] deca-3,7- Diene (common name: dicyclopentadiene), 7,8-benzotricyclo [4.3.0.12,5] dec-3-ene (common name: methanotetrahydrofluorene), tetracyclo [4.4.0. 12, 5.17,10] dodec-3-ene (common name: tetracyclododecene), derivatives of these compounds (for example, those having a substituent in the ring), and the like. The monomer having a norbornene structure may be one type or two or more types.

  Examples of the substituent that the ring may have include an alkyl group, an alkylene group, and a polar group. There may be a plurality of substituents, and they may be the same as or different from each other. Examples of polar groups include carboxyl groups, carbonyloxycarbonyl groups, epoxy groups, hydroxyl groups, oxy groups, ester groups, silanol groups, silyl groups, amino groups, nitrile groups, sulfone groups and the like.

  Examples of other monomers capable of ring-opening copolymerization with a monomer having a norbornene structure include monocyclic olefins such as cyclohexene, cycloheptene, and cyclooctene and derivatives thereof; cyclic conjugates such as cyclohexadiene and cycloheptadiene Diene and its derivatives are included.

  Examples of other monomers that can be addition copolymerized with a monomer having a norbornene structure include α-olefins having 2 to 20 carbon atoms such as ethylene, propylene, and 1-butene, and derivatives thereof; cyclobutene, cyclopentene, Examples include cycloolefins such as cyclohexene and derivatives thereof; non-conjugated dienes such as 1,4-hexadiene, 4-methyl-1,4-hexadiene, 5-methyl-1,4-hexadiene, and the like. Of these, α-olefins are preferable, and ethylene is more preferable. These monomers may be one kind or a combination of two or more kinds.

  A ring-opening (co) polymer or addition (co) polymer of a monomer having a norbornene structure is obtained by reacting a monomer having a norbornene structure in the presence of a known ring-opening polymerization catalyst or addition polymerization catalyst. It can be obtained by polymerization.

  A hydrogenated product of a ring-opening (co) polymer or addition (co) polymer of a monomer having a norbornene structure is a ring-opening (co) polymer or addition (co) polymer of a monomer having a norbornene structure. A known hydrogenation catalyst containing a transition metal such as nickel or palladium is added to this solution, and preferably 90% or more of the carbon-carbon unsaturated bonds are hydrogenated.

  Among norbornene-based resins, as a repeating unit, bicyclo [3.3.0] octane-2,4-diyl-ethylene structure (X) and tricyclo [4.3.0.12,5] decane-7, A resin having a 9-diyl-ethylene structure (Y) is preferred. The content of the repeating unit in such a norbornene-based resin is 90% by mass or more with respect to the entire repeating unit, and the mass ratio X: Y to the Y content is 100: 0 to 40. : 60 is preferable. Such a norbornene-based resin can give an optical film (retardation film) with little dimensional change and uniform optical characteristics.

  The molecular weight of the cyclic polyolefin is not particularly limited, but is a polyisoprene or polystyrene equivalent weight average molecular weight (Mw) measured by gel permeation chromatography using cyclohexane (toluene when the polymer resin is not dissolved) as a solvent. ) Is usually 20,000 to 150,000, preferably 25,000 to 100,000, more preferably 30,000 to 80,000. A film containing a cyclic polyolefin having a weight average molecular weight in the above range has good mechanical strength and moldability.

  The glass transition temperature of the cyclic polyolefin is not particularly limited, but is preferably 130 to 160 ° C, more preferably 135 to 150 ° C, from the viewpoint of enhancing the durability and stretchability of the resulting film. The molecular weight distribution (weight average molecular weight (Mw) / number average molecular weight (Mn)) of the cyclic polyolefin is 1.2 to 3.5, preferably 1.5 to 3.5 from the viewpoint of reducing the relaxation time and increasing the productivity. It is -3.0, More preferably, it is 1.8-2.7. The relaxation time refers to the time required for the relaxation treatment in which the film after stretching is heated for the purpose of making the optical properties of the obtained film uniform and adjusting the retardation value.

The absolute value of the photoelastic coefficient C of the film consisting of the cyclic polyolefin is preferably at ¹⁰ × 10 -12 ^{Pa -1} or less, more preferably 7 × ¹⁰ -12 ^{Pa -1} or less, 4 × ^{10 -12} More preferably, it is Pa- ¹ or less. The photoelastic coefficient C of a film made of cyclic polyolefin is a value represented by C = Δn / σ, where σ is the stress applied to the film and Δn is the birefringence of the film at that time.

  The transparent polymer substrate layer may further contain an additive as necessary. Examples of such additives include sugar ester compounds, polyester compounds, hydroxy group-terminated polyester compounds, and the like.

Sugar ester compound The sugar ester compound refers to a compound obtained by esterifying a hydroxyl group (hydroxyl group) of a saccharide and a carboxyl group of a monocarboxylic acid.

  Examples of sugars constituting the sugar ester compound include monosaccharides, disaccharides, and oligosaccharides to which 3 to 6 monosaccharides are bound. Of these, saccharides having 6 to 48 carbon atoms are preferable, and monosaccharides and disaccharides are more preferable.

  Examples of monosaccharides include glucose, fructose, arabinose, mannose, sorbitol and the like. Examples of disaccharides include sucrose, maltose and the like. Among these, glucose, fructose, and sucrose are preferable, and sucrose is more preferable because raw materials are easily available.

  The monocarboxylic acid constituting the sugar ester compound is not particularly limited, and may be a known aliphatic monocarboxylic acid, alicyclic monocarboxylic acid, or aromatic monocarboxylic acid. In order to easily develop the retardation of the film, an aromatic monocarboxylic acid is preferable. The monocarboxylic acid may be one kind or a mixture of two or more kinds. For example, an aliphatic monocarboxylic acid and an aromatic monocarboxylic acid may be combined.

  Examples of aliphatic monocarboxylic acids include acetic acid, propionic acid, butyric acid, isobutyric acid, valeric acid, caproic acid, enanthic acid, caprylic acid, pelargonic acid, capric acid, 2-ethyl-hexanecarboxylic acid, undecylic acid, lauric acid Saturated fatty acids such as acid, tridecylic acid, myristic acid, pentadecylic acid, palmitic acid, heptadecylic acid, stearic acid, nonadecanoic acid, arachidic acid, behenic acid, lignoceric acid, serotic acid, heptacosanoic acid, montanic acid, melicic acid, and laccelic acid Unsaturated fatty acids such as undecylenic acid, oleic acid, sorbic acid, linoleic acid, linolenic acid, arachidonic acid, octenoic acid and the like are included. The aliphatic monocarboxylic acid may further have a substituent such as an aryl group.

  Examples of the alicyclic monocarboxylic acid include cyclopentanecarboxylic acid, cyclohexanecarboxylic acid, and cyclooctanecarboxylic acid.

  The aromatic monocarboxylic acid is a monocarboxylic acid having one or more benzene rings, and the benzene ring may further have a substituent such as an alkyl group or an alkoxy group. Examples of aromatic monocarboxylic acids include benzoic acid, xylic acid, hemelitic acid, mesitylene acid, prenicylic acid, γ-isoduric acid, jurylic acid, mesitonic acid, α-isoduric acid, cumic acid, α-toluic acid, hydroatropa Acid, atropic acid, hydrocinnamic acid, salicylic acid, o-anisic acid, m-anisic acid, p-anisic acid, creosote acid, o-homosalicylic acid, m-homosalicylic acid, p-homosalicylic acid, o-pyrocatechuic acid, β-resorcylic acid, vanillic acid, isovanillic acid, veratromic acid, o-veratrumic acid, gallic acid, asaronic acid, mandelic acid, homoanisic acid, homovanillic acid, homoveratrumic acid, o-homoveratrumic acid, phthalonic acid, p-coumaric acid, etc. Among them, benzoic acid is particularly preferable.

  These monocarboxylic acids may further have a substituent such as an alkoxy group, an alkylthio group, a halogen atom, a cyano group, or a nitro group.

  The average ester substitution degree of the sugar ester compound whose constituent sugar is sucrose (the ratio of esterification with monocarboxylic acid among the eight hydroxyl groups contained in sucrose) is 1.0 or more, preferably 3. It is 0-8.0, More preferably, it is 3.5-7.5.

Especially, the sugar ester compound represented by the following general formula (1) and having an average degree of substitution of 3.5 to 7.5 is preferable.

R _{1 to} R ₈ in the formula (1) represent a substituted or unsubstituted alkylcarbonyl group or a substituted or unsubstituted arylcarbonyl group. R _{1 to} R ₈ may be the same as or different from each other.

  The substituted or unsubstituted alkylcarbonyl group is preferably a substituted or unsubstituted alkylcarbonyl group having 2 or more carbon atoms. Examples of the substituted or unsubstituted alkylcarbonyl group include a methylcarbonyl group (acetyl group). Examples of the substituent that the alkyl group has include an aryl group such as a phenyl group.

  The substituted or unsubstituted arylcarbonyl group is preferably a substituted or unsubstituted arylcarbonyl group having 7 or more carbon atoms. Examples of the arylcarbonyl group include a phenylcarbonyl group. Examples of the substituent that the aryl group has include an alkyl group such as a methyl group and an alkoxyl group such as a methoxy group.

Specific examples of the compound represented by the general formula (1) include the following. R in the table represents R _{1 to} R ₈ in the general formula (1).

  The content of the sugar ester compound is 0.5 to 30% by mass with respect to the resin component in order to suppress the change in retardation value due to the change in humidity of the optical film and stabilize the display quality. Preferably, it is 5-30 mass%, and it is especially preferable.

Polyester Compound The polyester compound is preferably a compound represented by the following general formula (2).
General formula (2)

  In formula (2), A represents a divalent group derived from an alkylene dicarboxylic acid having 4 to 12 carbon atoms or a divalent group derived from an aryl dicarboxylic acid having 8 to 14 carbon atoms. G is a divalent group derived from an alkylene glycol having 2 to 12 carbon atoms, a divalent group derived from an aryl glycol having 6 to 12 carbon atoms, or an oxyalkylene having 4 to 12 carbon atoms. Represents a divalent group derived from glycol. B represents a monovalent group derived from a hydrogen atom or a monocarboxylic acid. n represents an integer of 1 or more.

  Examples of the divalent group of A derived from an alkylene dicarboxylic acid having 4 to 12 carbon atoms include succinic acid, maleic acid, fumaric acid, glutaric acid, adipic acid, azelaic acid, sebacic acid, dodecanedicarboxylic acid And divalent groups derived from the above. Examples of divalent groups derived from aryl dicarboxylic acids having 8 to 14 carbon atoms in A include phthalic acid, terephthalic acid, isophthalic acid, 1,5-naphthalenedicarboxylic acid, 1,4-naphthalenedicarboxylic acid, etc. A divalent group derived from is included.

  Examples of the divalent group of G derived from an alkylene glycol having 2 to 12 carbon atoms include ethylene glycol, 1,2-propylene glycol, 1,3-propylene glycol, 1,2-butanediol, , 3-butanediol, 1,2-propanediol, 2-methyl-1,3-propanediol, 1,4-butanediol, 1,5-pentanediol, 2,2-dimethyl-1,3-propanediol (Neopentyl glycol), 2,2-diethyl-1,3-propanediol (3,3-dimethylolpentane), 2-n-butyl-2-ethyl-1,3-propanediol (3,3-didiol) Methylol heptane), 3-methyl-1,5-pentanediol, 1,6-hexanediol, 2,2,4-trimethyl-1,3-pentanediol, 2-ethyl-1,3-hexanediol, 2- Methyl-1,8-octanediol, 1, - nonanediol, include divalent groups derived from 1,10-decanediol, and 1,12-octadecanediol like.

  Examples of the divalent group of G derived from an aryl glycol having 6 to 12 carbon atoms include 1,2-dihydroxybenzene (catechol), 1,3-dihydroxybenzene (resorcinol), and 1,4-dihydroxy. Divalent groups derived from benzene (hydroquinone) and the like are included. Examples of the divalent group derived from oxyalkylene glycol having 4 to 12 carbon atoms in G are derived from diethylene glycol, triethylene glycol, tetraethylene glycol, dipropylene glycol, tripropylene glycol and the like. Divalent groups are included.

  G is preferably a divalent group derived from an alkylene glycol having 2 to 12 carbon atoms. This is to increase the compatibility of the polyester plasticizer with the cellulose ester.

  Examples of the monovalent group of B derived from monocarboxylic acid include benzoic acid, para-tert-butyl benzoic acid, orthotoluic acid, metatoluic acid, p-toluic acid, dimethyl benzoic acid, ethyl benzoic acid, and normal propyl benzoic acid. Monovalent groups derived from, for example, aromatic monocarboxylic acids such as aminobenzoic acid, and acetoxybenzoic acid; aliphatic monocarboxylic acids such as acetic acid, propionic acid, and butyric acid. Among these, B is preferably a monovalent group derived from an aromatic monocarboxylic acid.

  The number average molecular weight of the polyester compound is preferably 300 to 1500, and more preferably 400 to 1000. A polyester plasticizer having a number average molecular weight of less than 300 may be easily eluted from the optical film.

  The acid value of the polyester compound is preferably 0.5 mgKOH / g or less from the viewpoint of enhancing the adhesion between the optical film containing the polyester compound and another functional layer such as a hard coat layer, and the like. The following is more preferable. The acid value of the polyester compound is defined as the number of milligrams of potassium hydroxide required to neutralize the acid (carboxyl group present in the sample) contained in 1 g of the sample. The acid value of the polyester plasticizer can be measured according to JIS K0070.

  The hydroxyl value of the polyester compound is preferably 25 mgKOH / g or less, and more preferably 15 mgKOH / g or less, from the viewpoint of enhancing the compatibility with the cellulose ester. The hydroxyl value of the polyester compound is defined as the number of milligrams of potassium hydroxide required to neutralize unreacted acetic acid when 1 g of a sample is reacted with acetic anhydride and acetylated. The hydroxyl value of the polyester compound is measured according to JIS K 0070 (1992).

Specific examples of the polyester compound represented by the formula (2) are shown below.

  The mass ratio of the polyester compound and the sugar ester compound represented by the general formula (2) can be adjusted in the range of 99: 1 to 1:99. The total content of the polyester compound and the sugar ester compound represented by the general formula (2) is preferably 1 to 40% by mass with respect to the resin component.

The transparent polymer substrate layer may also contain a polyester compound (hydroxyl group-terminated polyester compound) represented by the general formula (3) as a polyester compound having positive birefringence.

  In formula (3), A represents an arylene group having 6 to 14 carbon atoms. As an example of the arylene group, a naphthalene group or a biphenylene group is preferable. The arylene group may further have a substituent such as an alkyl group having 1 to 6 carbon atoms, an alkenyl group, or an alkoxyl group. B represents a linear or branched alkylene group or cycloalkylene group having 2 to 6 carbon atoms. n represents a natural number of 1 or more.

  The polyester compound represented by the formula (3) is a compound obtained by reacting an aromatic dicarboxylic acid having 6 to 16 ring carbon atoms with a linear or branched alkylene diol or cycloalkylene diol having 2 to 6 carbon atoms. It is.

  Examples of the aromatic dicarboxylic acid having 6 to 16 carbon atoms include phthalic acid, isophthalic acid, terephthalic acid, 1,5-naphthalenedicarboxylic acid, 1,4-naphthalenedicarboxylic acid, 1,8-naphthalenedicarboxylic acid, 2, 3-naphthalenedicarboxylic acid, 2,6-naphthalenedicarboxylic acid, 2,8-naphthalenedicarboxylic acid, 2,2′-biphenyldicarboxylic acid, 4,4′-biphenyldicarboxylic acid, and the like, preferably 2,6- Naphthalenedicarboxylic acid, 4,4′-biphenyldicarboxylic acid.

  Examples of the linear or branched alkylene diol having 2 to 6 carbon atoms include ethylene glycol, 1,2-propanediol, 1,3-propanediol, 1,2-butanediol, 1,3-butanediol, 2-methyl-1,3-propanediol, 1,4-butanediol, 1,5-pentanediol, 3-methyl-1,5-pentanediol, 1,6-hexanediol and the like, preferably ethane Diol, 1,2-propanediol, 1,3-propanediol and 1,3-butanediol. Examples of the cycloalkylenediol include 1,4-cyclohexanediol, 1,4-cyclohexanedimethanol and the like.

  The hydroxyl value of the polyester compound represented by the formula (3) is preferably 100 to 500 mgKOH / g, and more preferably 170 to 400 mgKOH / g. When the hydroxyl value is more than 500 mgKOH / g, the hydrophobicity of the polyester compound represented by the formula (3) increases, so that the compatibility with the cellulose ester having a low acetyl substitution degree tends to be lowered. On the other hand, when the hydroxyl value is less than 100 mgKOH / g, the intermolecular interaction (hydrogen bond or the like) between the polyester compounds represented by the formula (3) becomes strong, and the compatibility with the cellulose ester tends to decrease. The hydroxyl value can be measured by the acetic anhydride method described in Japanese Industrial Standard JIS K1557-1: 2007.

The number average molecular weight (Mn) of the polyester compound represented by the formula (3) can be calculated from the following formula.
Mn = (number of hydroxyl groups in the molecule) × 56110 / (hydroxyl value) = 2 × 56110 / (hydroxyl value)

The specific example of the polyester compound represented by Formula (3) below is shown.

  The content of the polyester compound represented by the formula (3) is preferably 1% by mass or more and less than 5% by mass with respect to the resin component.

Other additives The transparent polymer substrate layer may further contain other additives as necessary. Examples of such additives include retardation increasing agents, plasticizers, antioxidants, acid scavengers, light stabilizers, ultraviolet absorbers, optical anisotropy control agents, matting agents, antistatic agents, release agents. Etc. are included.

  The retardation raising agent is preferably an aromatic compound having two or more aromatic rings. One type of retardation raising agent may be sufficient, and a 2 or more types of mixture may be sufficient as it.

  The aromatic ring contained in the aromatic compound is an aromatic hydrocarbon ring or an aromatic heterocycle. The aromatic hydrocarbon ring is preferably a 6-membered ring (benzene ring). The aromatic heterocycle is a 5-membered ring, 6-membered ring or 7-membered ring, preferably a 5-membered ring or 6-membered ring. The hetero atom contained in the aromatic heterocycle is a nitrogen atom, an oxygen atom or a sulfur atom, preferably a nitrogen atom.

  Examples of aromatic heterocycles include furan ring, thiophene ring, pyrrole ring, oxazole ring, isoxazole ring, thiazole ring, isothiazole ring, imidazole ring, pyrazole ring, furazane ring, triazole ring, pyran ring, pyridine ring , Pyridazine ring, pyrimidine ring, pyrazine ring and 1,3,5-triazine ring, preferably 1,3,5-triazine ring. Specific examples of the aromatic compound include compounds described in JP-A No. 2004-109410, JP-A No. 2003-344655, JP-A No. 2000-275434, JP-A No. 2000-1111914, JP-A No. 12-275434, and the like. included.

  The content of the retardation increasing agent is preferably 0.01 to 20% by mass, more preferably 0.05 to 15% by mass with respect to the resin component contained in the transparent polymer substrate layer. More preferably, it is 1-10 mass%.

Fine particles The transparent polymer substrate layer may further contain fine particles in order to improve slipperiness. The fine particles may be inorganic fine particles or organic fine particles.

  Examples of inorganic fine particles include silicon dioxide, titanium dioxide, aluminum oxide, zirconium oxide, calcium carbonate, calcium carbonate, talc, clay, calcined kaolin, calcined calcium silicate, hydrated calcium silicate, aluminum silicate, magnesium silicate And calcium phosphate. Examples of the organic fine particles include silicone resin fine particles, fluororesin fine particles, acrylic resin fine particles, and the like, preferably silicone resin fine particles. Among these, in order to reduce the increase in haze of the transparent polymer substrate layer, fine particles containing silicon are preferable, and silicon dioxide is particularly preferable.

  Examples of the silicon dioxide fine particles include Aerosil R972, R972V, R974, R812, 200, 200V, 300, R202, OX50, TT600 (commercially available from Nippon Aerosil Co., Ltd.). Of these, Aerosil 200V and Aerosil R972V are preferred because of the great effect of reducing the friction coefficient while keeping the haze of the protective film low. Examples of the fine particles of zirconium oxide include Aerosil R976 and R811 (trade names manufactured by Nippon Aerosil Co., Ltd.).

  The primary average particle diameter of the fine particles is preferably 5 to 400 nm, and more preferably 10 to 300 nm.

  The fine particles are preferably contained in the transparent polymer substrate layer so that the dynamic friction coefficient of at least one surface of the transparent polymer substrate layer is 0.2 to 1.0. The content of the fine particles is preferably 0.01 to 1% by mass and more preferably 0.05 to 0.5% by mass with respect to the transparent polymer substrate layer.

  However, it is preferable that the transparent polymer substrate layer containing cyclic polyolefin does not substantially contain fine particles. The phrase “substantially free of fine particles” includes the case of containing fine particles in an amount in a range in which the amount of increase from the haze of the cyclic polyolefin film not containing fine particles is 0.05% or less. Among the cyclic polyolefins, alicyclic polyolefins have low affinity with organic fine particles and inorganic fine particles. Therefore, a film obtained by stretching a cyclic polyolefin film containing fine particles is likely to generate voids and has high haze. .

Physical properties of the transparent polymer substrate layer The thickness of the transparent polymer substrate layer is not particularly limited, but is preferably 20 to 200 μm, more preferably 20 to 100 μm, still more preferably 20 to 60 μm, It is especially preferable that it is 20-40 micrometers. If the thickness of the optical film is too large, the variation in retardation tends to increase due to humidity. On the other hand, if the thickness of the film is too small, it is difficult to obtain a desired retardation.

When a protective film having a specific resin layer is used as a retardation film of a VA liquid crystal cell, the environment of the transparent polymer substrate layer contained in the protective film having the specific resin layer is 23 ° C. and 55% RH. Below, it is preferable that the retardation Ro measured at wavelength 590nm is 20-100nm. The retardation Rth measured at a wavelength of 590 nm in an environment of 23 ° C. and 55% RH is preferably 70 to 300 nm. The retardations _R0 and Rth of the optical film can usually be adjusted by stretching conditions.

The in-plane direction retardation R ₀ and the thickness direction retardation Rth are each expressed by the following equations.
Formula (I) R ₀ = (nx−ny) × d
Formula (II) Rth = {(nx + ny) / 2−nz} × d
(Nx: refractive index in the slow axis direction in the film plane, ny: refractive index in the direction perpendicular to the slow axis in the film plane, nz: refractive index of the film in the thickness direction, d: film thickness (Nm))

The retardations _R0 and Rth can be determined by the following method, for example.
1) The average refractive index of the film is measured with a refractometer.
2) The retardation _R0 in the in-plane direction when light having a wavelength of 590 nm from the normal direction of the film is incident is measured by KOBRA-21ADH manufactured by Oji Scientific Instruments.
3) The retardation value R (θ) when light having a wavelength of 590 nm is incident from the angle θ (incident angle (θ)) with respect to the film normal direction is measured by KOBRA-21ADH manufactured by Oji Scientific Instruments. . θ is larger than 0 °, preferably 30 ° to 50 °.
4) From the measured R ₀ and R (θ) and the above-described average refractive index and film thickness, nx, ny and nz are calculated by KOBRA-21ADH manufactured by Oji Scientific Instruments, and Rth is calculated. The measurement of retardation can be performed under conditions of 23 ° C. and 55% RH.

  The transparent polymer substrate layer has a slow axis or a fast axis in the film plane. The angle θ1 (orientation angle) between the slow axis and the film forming direction is preferably −5 ° or more and + 5 ° or less, more preferably −1 ° or more and + 1 ° or less, and −0.5 °. More preferably, it is + 0.5 ° or less, and particularly preferably −0.1 ° or more and + 0.1 ° or less. Since the light leakage can be suppressed when the orientation angle θ1 satisfies the above range, the luminance of the display image can be increased. The orientation angle θ1 can be adjusted depending on the stretching conditions.

The retardation _R0 and Rth of the transparent polymer base material layer and the orientation angle θ1 can be measured using an automatic birefringence meter KOBRA-21ADH (Oji Scientific Instruments).

The internal haze of the transparent polymer substrate layer measured according to JIS K-7136 is preferably 0.05% or less, and more preferably 0.03% or less. The moisture permeability of the protective film at 40 ° C. and 90% RH measured in accordance with JIS Z 0208 is preferably 10 to 1200 g / m ² · 24 h. In order to reduce the moisture permeability of the transparent polymer substrate layer, for example, the thermoplastic resin contained in the transparent polymer substrate layer is a cyclic olefin resin, a (meth) acrylic resin or a cellulose ester having a high degree of acyl group substitution, A lot of additives such as a plasticizer may be contained.

  The visible light transmittance of the transparent polymer substrate layer is preferably 90% or more, and more preferably 93% or more. The breaking elongation of the optical film of the present invention is preferably 10 to 80%.

  The film to be the transparent polymer substrate layer can be preferably produced by a solution casting method or a melt casting method. Hereinafter, the manufacturing method of the film containing a cellulose ester is demonstrated.

A) Solution Casting Method A method for producing a film to be a transparent polymer substrate layer by a solution casting method is as follows: A-1) A step of preparing a dope by dissolving at least the aforementioned cellulose ester in a solvent (dope preparation step) ), A-2) Step of casting dope on endless metal support (casting step), A-3) Step of evaporating solvent from cast dope to form web (solvent evaporation step), A -4) Step of peeling the web from the metal support (peeling step), A-5) Step of drying the web and drawing it to obtain a film (drying and drawing step), A-6) Winding the obtained film A step of taking (winding step).

A-1) Dope preparation step In a dissolution vessel, a dope is prepared by dissolving a thermoplastic resin and, if necessary, an additive in a solvent. The solvent used for preparing the dope is not particularly limited as long as it dissolves a thermoplastic resin such as cellulose ester. Examples of such solvents include chlorinated organic solvents such as methylene chloride; methyl acetate, ethyl acetate, amyl acetate, acetone, tetrahydrofuran, 1,3-dioxolane, 1,4-dioxane, cyclohexanone, ethyl formate, 2, 2,2-trifluoroethanol, 2,2,3,3-hexafluoro-1-propanol, 1,3-difluoro-2-propanol, 1,1,1,3,3,3-hexafluoro-2- Methyl-2-propanol, 1,1,1,3,3,3-hexafluoro-2-propanol, 2,2,3,3,3-pentafluoro-1-propanol, nitroethane, ethyl lactate, lactic acid, di Non-chlorine organic solvents such as acetone alcohol are included, and methylene chloride, methyl acetate, ethyl acetate, acetone, and ethyl lactate are preferable.

  The solvent used for the preparation of the dope may further contain a solvent other than those described above. Examples of such other solvents include linear or branched aliphatic alcohols having 1 to 4 carbon atoms. Examples of linear or branched aliphatic alcohols having 1 to 4 carbon atoms include methanol, ethanol, n-propanol, iso-propanol, n-butanol, sec-butanol, tert-butanol and the like, Ethanol is preferred because it has a relatively low boiling point and is easy to dry.

  The content of the other solvent may be 1 to 40% by mass with respect to the whole solvent. When the content ratio of the other solvent is increased, the resulting web is easily gelled, and thus easily peeled from the metal support. On the other hand, when the content ratio of the other solvent in the dope is lowered, the thermoplastic resin is easily dissolved when the solvent is a non-chlorine organic solvent.

  The content of the thermoplastic resin in the dope containing methylene chloride and a linear or branched aliphatic alcohol having 1 to 4 carbon atoms as the solvent is preferably 10 to 45% by mass.

  The thermoplastic resin is dissolved at normal pressure, at a temperature lower than the boiling point of the main solvent, at a temperature higher than the boiling point of the main solvent and under pressure, Japanese Patent Application Laid-Open No. 9-95544, Japanese Patent Application Laid-Open No. 9-95557, or Japanese Patent Application Laid-Open No. The method may be a method performed by a cooling dissolution method described in JP-A-9-95538, a method performed under high pressure described in JP-A No. 11-21379, and a method performed more than the boiling point of the main solvent and under pressure is particularly preferable.

A-2) Casting step The dope is fed to a pressure die through a liquid feed pump (for example, a pressurized metering gear pump), and is placed on an endless metal support (for example, a stainless steel belt or a rotating metal drum). And casting from the slit of the pressure die.

  The die is preferably a pressure die that can adjust the slit shape of the die portion and easily adjust the film thickness uniformly. Examples of the pressure die include a coat hanger die and a T-die. The surface of the metal belt is preferably mirror-finished.

A-3) Solvent evaporation step A web (dope film obtained by casting a dope on a metal support) is heated on the metal support to evaporate the solvent. The web is preferably dried in an atmosphere of 40 to 100 ° C. In order to dry the web in an atmosphere of 40 to 100 ° C., it is preferable to apply hot air of 40 to 100 ° C. to the upper surface of the web or to heat it with infrared rays or the like.

  As a method for evaporating the solvent, there are a method in which air is applied to the surface of the web, a method in which heat is transferred from the back surface of the belt by liquid, a method in which heat is transferred from the front and back by radiant heat, etc. A method in which heat is transferred from the back surface with a liquid is preferable.

A-4) Peeling process The web from which the solvent has evaporated on the metal support is peeled off at the peeling position. The temperature at the peeling position on the metal support is preferably 10 to 40 ° C, more preferably 11 to 30 ° C.

The residual solvent amount of the web at the time of peeling at the peeling position on the metal support is preferably 50 to 120% by mass, although it depends on the drying conditions and the length of the metal support. A web having a large amount of residual solvent is too soft and tends to impair flatness, and is liable to cause slippage and vertical stripes due to peeling tension. The residual solvent amount of the web at the peeling position can be set so that such slippage and vertical stripes can be suppressed.
The amount of residual solvent in the web is defined by the following formula.
Residual solvent amount (%) = (mass before web heat treatment−mass after web heat treatment) / (mass after web heat treatment) × 100
The heat treatment for measuring the residual solvent amount means a heat treatment at 115 ° C. for 1 hour.

  The peeling tension at the time of peeling the web from the metal support is usually 196 to 245 N / m, but it is preferably 190 N / m or less when wrinkles easily occur at the time of peeling. m or less is more preferable, 137.2 N / m or less is more preferable, and 100 N / m or less is further preferable.

  The web temperature at the peeling position on the metal support is preferably -50 to 40 ° C, more preferably 10 to 40 ° C, and further preferably 15 to 30 ° C.

A-5) Drying and stretching step The web obtained by peeling from the metal support is dried and then stretched. For drying the web, the web may be dried while being transported by a large number of rolls arranged vertically, or may be dried while being transported while fixing both ends of the web with clips.

  The method for drying the web may be a method of drying with hot air, infrared rays, a heating roll, microwave, or the like, and a method of drying with hot air is preferable because it is simple. The drying temperature of the web is 40 to 250 ° C, preferably 40 to 160 ° C. Drying at high temperature is preferably carried out with the residual solvent amount of the web being 8% by mass or less.

  A transparent polymer substrate layer having a desired retardation is obtained by stretching the web. The retardation of the transparent polymer substrate layer can be controlled by adjusting the magnitude of the tension applied to the web at least in the direction perpendicular to the web conveyance direction (width direction).

  The web may be stretched at least in the width direction, and may be uniaxial stretching or biaxial stretching. The web may be stretched in the width direction or in an oblique direction with respect to the dope casting direction. Biaxial stretching includes stretching in both the casting direction (longitudinal direction) and the width direction (lateral direction) of the dope. Biaxial stretching may be sequential biaxial stretching or simultaneous biaxial stretching.

Sequential biaxial stretching includes a method in which stretching in different stretching directions is sequentially performed, a method in which stretching in the same direction is performed in multiple stages, and the like. Examples of sequential biaxial stretching include the following stretching steps.
Stretch in the casting direction-Stretch in the width direction-Stretch in the casting direction-Stretch in the casting direction Stretch in the width direction-Stretch in the width direction-Stretch in the casting direction-Stretch in the casting direction

  Simultaneous biaxial stretching also includes a mode in which stretching is performed in one direction and the tension in the other direction is relaxed and contracted. The stretching ratio in the case of simultaneous biaxial stretching is preferably 1.01 to 1.5 times in both the width direction and the casting direction.

  The method of stretching the web is not particularly limited, and a method in which a difference in peripheral speed is applied to a plurality of rolls and the roll is stretched in the longitudinal direction using the difference in the peripheral speed of the roll (roll stretching method). The clip and pin spacing is widened in the vertical direction and stretched in the vertical direction, widened in the horizontal direction and stretched in the horizontal direction, or stretched in both the vertical and horizontal directions and stretched in both the vertical and horizontal directions (tenter stretching, etc. Law). These stretching methods may be combined.

  The residual solvent amount of the web at the start of tenter stretching is preferably 20 to 100% by mass. Further, the residual solvent amount of the web after tenter stretching is preferably 10% by mass or less, and more preferably 5% by mass or less.

  The web stretching temperature is preferably 30 to 160 ° C, more preferably 50 to 150 ° C, and further preferably 70 to 140 ° C. In order to increase the uniformity of the obtained transparent polymer substrate layer, it is preferable that the temperature distribution in the width direction of the atmosphere in the tenter stretching step is small, and the temperature distribution in the width direction is preferably within ± 5 ° C., Within 2 ° C is more preferable, and within ± 1 ° C is more preferable.

  The tenter stretching device is preferably capable of independently controlling the web grip length (distance from the start of gripping to the end of gripping) on the left and right. Moreover, it is preferable that a tenter process has a different temperature area | region and has a neutral zone between different temperature areas, in order to improve the planarity of the transparent polymer base material layer obtained.

A-6) Winding process The film obtained by extending | stretching a web is wound up with a winder. The residual solvent amount of the film to be wound is preferably 2% by mass or less, more preferably 0.4% by mass or less, and further preferably 0.10% by mass or less in order to improve dimensional stability. is there.

  The winding method is not particularly limited, and includes a constant torque method, a constant tension method, a taper tension method, a program tension control method with a constant internal stress, and the like.

  The obtained transparent polymer base material layer is a long film, and usually has a length of about 100 m to 10000 m. Moreover, it is preferable that the width | variety of a transparent polymer base material layer is 1.3-4 m, and it is more preferable that it is 1.4-2.5 m.

B) Melt Casting Method A film to be a transparent polymer substrate layer is produced by the melt casting method. B-1) Step for producing molten pellets (pelletizing step), B-2) Melting and kneading the molten pellets After that, an extruding step (melt extrusion step), B-3) a step of cooling and solidifying the molten resin to obtain a web (cooling solidification step), and B-4) a step of stretching the web (stretching step) are included.

B-1) Pelletization process It is preferable that the resin composition containing the thermoplastic resin constituting the film to be the transparent polymer substrate layer is previously kneaded and pelletized. Pelletization can be performed by a known method. For example, a resin composition containing the above-described thermoplastic resin and, if necessary, an additive such as a plasticizer is melt-kneaded in an extruder, and then die-molded. Extruded into strands. The molten resin extruded in a strand shape can be cooled with water or air, and then cut to obtain pellets.

  In order to prevent decomposition, the raw material of the pellet is preferably dried before being supplied to the extruder. For example, since a cellulose ester as a thermoplastic resin is easy to absorb moisture, it is preferable to dry at 70 to 140 ° C. for 3 hours or more so that the moisture content is 200 ppm or less, preferably 100 ppm or less.

The mixture of the antioxidant and the thermoplastic resin may be mixed with each other; the antioxidant dissolved in the solvent may be impregnated into the thermoplastic resin; and the antioxidant may be mixed. You may spray and mix in a thermoplastic resin. A vacuum nauter mixer or the like is preferable because the raw materials can be dried and mixed at the same time. Further, the atmosphere around the feeder portion of the extruder and the outlet portion of the die is preferably an atmosphere of dehumidified air or N ₂ gas in order to prevent deterioration of the raw material of the pellet.

  In an extruder, it is preferable to knead at a low shearing force or at a low temperature so as not to cause deterioration of the resin (decrease in molecular weight, coloring, gel formation, etc.). For example, when kneading with a twin-screw extruder, it is preferable to use a deep groove type screw and rotate the two screws in the same direction. In order to knead uniformly, it is preferable that two screw shapes mesh with each other.

  Instead of pelletizing the resin composition containing the thermoplastic resin, a film that becomes a transparent polymer substrate layer may be produced by melt-kneading in an extruder using a thermoplastic resin that has not been melt-kneaded as a raw material.

B-2) Melt Extrusion Step The obtained molten pellets and other additives as necessary are supplied from the hopper to the extruder. The supply of pellets is preferably performed under vacuum, reduced pressure, or an inert gas atmosphere in order to prevent oxidative decomposition of the pellets. Then, in an extruder, the molten pellets and, if necessary, other additives (film material) are melt-kneaded.

  The melting temperature of the film material in the extruder is preferably in the range of Tg ° C to (Tg + 100) ° C, more preferably (Tg ° C) when the glass transition temperature of the film is Tg ° C, although it depends on the type of film material. It is the range of Tg + 10) ° C. to (Tg + 90) ° C. The residence time of the film material in the extruder is preferably 5 minutes or less. The residence time can be adjusted by the number of rotations of the screw, the depth of the groove, L / D which is the ratio of the cylinder length (L) to the cylinder inner diameter (D), and the like.

  The molten resin extruded from the extruder is filtered through a leaf disk filter or the like as necessary, and further mixed with a static mixer or the like, and extruded from a die into a film. The melting temperature Tm of the resin at the exit portion of the die can be about 200 to 300 ° C.

  If foreign matter such as scratches or plasticizer aggregates adheres to the inner wall surface of the die, streaky defects (die lines) may occur on the surface of the extruded molten resin. In order to reduce surface defects such as die lines, the inner wall surface from the extruder to the tip of the die should have a structure in which the resin staying part is difficult to adhere; for example, the inner wall surface from the extruder to the tip of the die. Is preferably free from scratches.

  In order to make it difficult for the molten resin to adhere to the inner wall surface of an extruder, die, or the like, it is preferable that surface treatment is performed to reduce the surface roughness or the surface energy. Examples of such surface processing include processing for polishing to have a surface roughness of 0.2 S or less after hard chrome plating or ceramic spraying.

B-3) Cooling and solidifying step The resin extruded from the die is nipped between the cooling roll and the elastic touch roll to make the film-like molten resin a predetermined thickness. Then, the film-like molten resin is cooled stepwise with a plurality of cooling rolls and solidified.

  The surface temperature Tr1 of the cooling roll can be Tg (° C.) or lower when the glass transition temperature of the obtained film is Tg (° C.). The surface temperatures of the plurality of cooling rolls may be different. The film surface temperature Tt on the elastic touch roll side can be (Tr1-50) ° C. ≦ Tt ≦ (Tr1-5) ° C.

  The cooling roll is a high-rigidity metal roll and has a structure in which a temperature-controllable medium can be circulated. The material of the surface of the cooling roll can be stainless steel, aluminum, titanium, or the like. The surface of the cooling roll may be subjected to a surface treatment such as hard chrome plating, nickel plating, amorphous chrome plating, ceramic spraying, etc. in order to make the resin easy to peel off. In order to keep the haze of the film low, the surface roughness Ra of the cooling roll is preferably 0.1 μm or less, and more preferably 0.05 μm or less. The size of the cooling roll only needs to be large enough to cool the extruded film-like molten resin, and the diameter of the cooling roll is usually about 100 mm to 1 m.

  The elastic touch rolls are disclosed in JP-A-03-124425, JP-A-08-224772, JP-A-07-1000096, JP-A-10-272676, WO97 / 028950, JP-A-11-235747, JP-A-11-235747. Silicon rubber rolls covered with a thin film metal sleeve described in JP-A-2002-36332, JP-A-2005-172940, and JP-A-2005-280217 are used.

  The film-like molten resin solidified from the cooling roll is peeled off with a peeling roll or the like to obtain a web. When peeling the film-like molten resin, it is preferable to adjust the tension in order to prevent deformation of the resulting web.

B-4) Stretching step The obtained web is stretched with a stretching machine to obtain a film. The stretching may be performed in at least one direction, and is preferably performed in both the web width direction (TD direction) and the web conveyance direction (MD direction).

  When stretching in both the web width direction (TD direction) and the web conveyance direction (MD direction), the web width direction (TD direction) stretching and the web conveyance direction (MD direction) stretching are sequential. Or may be performed simultaneously.

  The draw ratio can be 1.01 to 3.0 times, preferably 1.1 to 2.0 times in each direction. When extending in both the web width direction (TD direction) and the web conveyance direction (MD direction), the final direction is 1.01 to 3.0 times, preferably 1.1 to 2.0 times in each direction. It is preferable to do.

  The stretching temperature is preferably Tg to (Tg + 50) ° C. The stretching temperature is preferably uniform in the width direction of the web (TD direction) or the transport direction (MD direction), and the variation in the width direction or transport direction of the web stretching temperature is preferably ± 2 ° C. or less, The temperature is more preferably ± 1 ° C. or less, and further preferably ± 0.5 ° C. or less.

  For stretching the web, a roll stretching machine or a tenter stretching machine can be used. For example, when obtaining a protective film, it is preferable to extend | stretch in the width direction (TD direction) of a web. The web stretched in the width direction has an in-plane slow axis parallel to the width direction. Therefore, generally, if a polarizer having an absorption axis parallel to the longitudinal direction of the web (MD direction) and a protective film having an in-plane slow axis parallel to the width direction are laminated by roll-to-roll, The absorption axis of the polarizer and the in-plane slow axis of the protective film can be made orthogonal.

  In order to adjust the retardation of the film obtained after stretching or to reduce the dimensional change, the film obtained after stretching is shrunk in the transport direction (MD direction) or the width direction (TD direction) as necessary. May be. To shrink the film obtained after stretching in the transport direction (MD direction), for example, release the clip gripped in the width direction and loosen it in the transport direction; gradually reduce the interval between adjacent clips in the transport direction. To relax in the transport direction.

C) Co-casting method The transparent polymer substrate layer having a multilayer structure can be preferably produced by a co-casting method. In the co-casting method, two or more kinds of polymer solutions containing a thermoplastic resin or the like are cast on a smooth support (band or drum). The co-casting method is a method of sequentially laminating a solution containing a polymer from a plurality of casting ports provided at different positions in the casting direction to form a multi-layer web (sequential lamination co-casting). Or a method in which polymer solutions are simultaneously cast from a plurality of casting ports provided at the same position in the casting direction and laminated to form a multilayer web (simultaneous lamination co-casting). May be. Examples of the sequential lamination co-casting method include the methods described in JP-A Nos. 61-158414, 1-122419, and 11-198285. Examples of simultaneous lamination and co-casting include Japanese Patent Publication Nos. 60-27562, 61-94724, 61-947245, 61-104413, 61-158413, There is a method described in Kaihei 6-134933.

  In the simultaneous lamination co-casting method, as described in JP-A No. 56-162617, a high-viscosity polymer solution is circulated in the center, and a low-viscosity polymer solution is circulated around the outer periphery to form a cylindrical shape. A method of extruding two laminated polymer solutions simultaneously is also included. Further, as described in JP-A-61-94724 and JP-A-61-94725, the content of the poor solvent (specifically, alcohol component) of the polymer solution flowing in the outer peripheral part is changed to the central part. It is also preferred that the amount be larger than the polymer solution flowing through.

  In the co-casting, the thickness of the layer not contacting the metal support (outer layer) among the layer contacting the metal support (inner layer) and the layer not contacting the metal support (outer layer) is preferably It is 1 to 50% of the total film thickness, and more preferably 2 to 30%. For example, in the case of co-casting with three or more layers, the outer layer means the total film thickness of layers other than the layer in contact with the metal support.

  Using polymer solutions having different concentrations of additives (for example, compounds having negative birefringence, compounds having positive birefringence, plasticizers, ultraviolet absorbers, matting agents, etc.) For example, a film having a laminated structure of skin layer / core layer / skin layer can be obtained.

  For example, the matting agent, the plasticizer, or the ultraviolet absorber may be contained in the core layer more than the skin layer, or may be contained only in the core layer. Further, the skin layer may contain a low-volatile plasticizer or an ultraviolet absorber, and the core layer may contain a plasticizer having excellent plasticity or an ultraviolet absorber having excellent ultraviolet absorption. Further, the release agent may be contained only in the skin layer on the metal support side. Further, the Tg of the skin layer and the core layer may be different, and the Tg of the core layer may be lower than the Tg of the skin layer.

  In the case where the metal support is cooled and the solution is gelled and peeled off, alcohol that is a poor solvent may be contained in the polymer solution for the skin layer more than the polymer solution for the core layer. Also, the viscosity of the polymer solution during casting may be different between the polymer solution for the skin layer and the polymer solution for the core layer.

About a specific resin layer A specific resin layer is arrange | positioned on the surface of the above-mentioned transparent polymer base material layer. The specific resin layer includes a thermoplastic resin including a polyether unit, a polyester unit, or a polyacryl unit.

  The polyether unit is a unit containing an oxyalkylene group as a repeating unit. Examples of the thermoplastic resin including a polyether unit include polyether, polyether urethane described later, and the like. The polyester unit is a unit composed of a condensation polymer of dicarboxylic acid and diol. Examples of the thermoplastic resin including a polyester unit include polyester, polyester urethane described later, and the like. The polyacryl unit is a unit composed of an addition polymer of (meth) acrylic acid ester. Examples of the thermoplastic resin including a polyacryl unit include polyacryl urethane described later.

  These thermoplastic resins may be one kind or a mixture of two or more kinds. Of these, urethane resin is preferable in order to increase the adhesive force between the transparent polymer substrate layer and the polarizer.

  The urethane resin is usually obtained by reacting a polyol and a polyisocyanate. The polyol is a compound having two or more hydroxyl groups in the molecule, and specific examples thereof include polyacryl polyol, polyester polyol, polyether polyol and the like. For example, the resin obtained by reacting polyester polyol and polyisocyanate is polyester urethane. A resin obtained by reacting a polyether polyol and a polyisocyanate is a polyether urethane resin. These may be one kind or a mixture of two or more kinds.

  The polyacryl polyol is obtained by copolymerizing a (meth) acrylic acid ester and a monomer having a hydroxyl group. Examples of (meth) acrylic acid esters include methyl (meth) acrylate, butyl (meth) acrylate, 2-ethylhexyl (meth) acrylate, cyclohexyl (meth) acrylate, and the like. Examples of the monomer having a hydroxyl group include 2-hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate, 3-hydroxypropyl (meth) acrylate, and 2-hydroxy (meth) acrylate. Hydroxyalkyl esters of (meth) acrylic acid such as butyl, 4-hydroxybutyl (meth) acrylate, 2-hydroxypentyl (meth) acrylate; mono (meth) acrylic acid of polyhydric alcohols such as glycerin and trimethylolpropane Ester; N-methylol (meth) acrylamide and the like are included. These may be one kind or a mixture of two or more kinds.

  The polyacryl polyol may be obtained by copolymerizing a (meth) acrylic acid ester, a monomer having a hydroxyl group, and another monomer. Examples of other monomers include unsaturated monocarboxylic acids such as (meth) acrylic acid; unsaturated dicarboxylic acids such as maleic acid, anhydrides or mono- or diesters thereof; unsaturated nitriles such as (meth) acrylonitrile Unsaturated amides such as (meth) acrylamide and N-methylol (meth) acrylamide; Vinyl esters such as vinyl acetate and vinyl propionate; Vinyl ethers such as methyl vinyl ether; α-olefins such as ethylene and propylene; Halogenated α, β-unsaturated aliphatic monomers such as vinyl chloride and vinylidene chloride; α, β-unsaturated aromatic monomers such as styrene and α-methylstyrene are included. These may be one kind or a mixture of two or more kinds.

  The polyester polyol is obtained by reacting a polybasic acid and a polyol. Examples of polybasic acids include orthophthalic acid, isophthalic acid, terephthalic acid, 1,4-naphthalenedicarboxylic acid, 2,5-naphthalenedicarboxylic acid, 2,6-naphthalenedicarboxylic acid, biphenyldicarboxylic acid, tetrahydrophthalic acid, etc. Aromatic dicarboxylic acids; oxalic acid, succinic acid, malonic acid, glutaric acid, adipic acid, pimelic acid, suberic acid, azelaic acid, sebacic acid, decanedicarboxylic acid, dodecanedicarboxylic acid, octadecanedicarboxylic acid, tartaric acid, alkylsuccinic acid, Aliphatic dicarboxylic acids such as linolenic acid, maleic acid, fumaric acid, mesaconic acid, citraconic acid, itaconic acid; hexahydrophthalic acid, tetrahydrophthalic acid, 1,3-cyclohexanedicarboxylic acid, 1,4-cyclohexanedicarboxylic acid, etc. Alicyclic dicarboxylic acid; These acid anhydrides, alkyl esters, reactive derivatives such as acid halides. These may be one kind or a mixture of two or more kinds.

  Examples of polyols constituting the polyester polyol include ethylene glycol, 1,2-propanediol, 1,3-propanediol, 1,3-butanediol, 1,4-butanediol, neopentyl glycol, pentanediol, 1 , 6-hexanediol, 1,8-octanediol, 1,10-decanediol, 1-methyl-1,3-butylene glycol, 2-methyl-1,3-butylene glycol, 1-methyl-1,4- Pentylene glycol, 2-methyl-1,4-pentylene glycol, 1,2-dimethyl-neopentyl glycol, 2,3-dimethyl-neopentyl glycol, 1-methyl-1,5-pentylene glycol, 2- Methyl-1,5-pentylene glycol, 3-methyl-1,5-pentylene glycol, , 2-dimethylbutylene glycol, 1,3-dimethylbutylene glycol, 2,3-dimethylbutylene glycol, 1,4-dimethylbutylene glycol, diethylene glycol, triethylene glycol, polyethylene glycol, dipropylene glycol, polypropylene glycol, 1,4 -Cyclohexanedimethanol, 1,4-cyclohexanediol, bisphenol A, bisphenol F, hydrogenated bisphenol A, hydrogenated bisphenol F, and the like. These may be one kind or a mixture of two or more kinds.

  The polyether polyol is obtained by subjecting an alkylene oxide to ring-opening addition polymerization to a polyhydric alcohol. Examples of the polyhydric alcohol include ethylene glycol, diethylene glycol, propylene glycol, dipropylene glycol, glycerin, trimethylolpropane and the like. Examples of the alkylene oxide include ethylene oxide, propylene oxide, butylene oxide, styrene oxide, tetrahydrofuran and the like. These may be one kind or a mixture of two or more kinds.

Examples of polyisocyanates include tetramethylene diisocyanate, dodecamethylene diisocyanate, 1,4-butane diisocyanate, hexamethylene diisocyanate, 2,2,4-trimethylhexamethylene diisocyanate, 2,4,4-trimethylhexamethylene diisocyanate, lysine diisocyanate. Aliphatic diisocyanates such as 2-methylpentane-1,5-diisocyanate, 3-methylpentane-1,5-diisocyanate;
Cycloaliphatic diisocyanates such as isophorone diisocyanate, hydrogenated xylylene diisocyanate, 4,4'-cyclohexylmethane diisocyanate, 1,4-cyclohexane diisocyanate, methylcyclohexylene diisocyanate, 1,3-bis (isocyanatomethyl) cyclohexane;
Tolylene diisocyanate, 2,2'-diphenylmethane diisocyanate, 2,4'-diphenylmethane diisocyanate, 4,4'-diphenylmethane diisocyanate, 4,4'-diphenyldimethylmethane diisocyanate, 4,4'-dibenzyldiisocyanate, 1,5 -Aromatic diisocyanates such as naphthylene diisocyanate, xylylene diisocyanate, 1,3-phenylene diisocyanate, 1,4-phenylene diisocyanate;
Examples include araliphatic diisocyanates such as dialkyldiphenylmethane diisocyanate, tetraalkyldiphenylmethane diisocyanate, and α, α, α, α-tetramethylxylylene diisocyanate. These may be one kind or a mixture of two or more kinds.

  Among these, a urethane resin having a carboxyl group is preferable. This is because the protective film containing a carboxyl group-containing urethane resin has high adhesion to a polarizer, particularly under high temperature and high humidity.

  The urethane resin having a carboxyl group can be obtained, for example, by further copolymerizing a chain extender having a free carboxyl group in addition to the aforementioned polyol and polyisocyanate. Examples of the chain extender having a free carboxyl group include dihydroxycarboxylic acid, dihydroxysuccinic acid and the like. Examples of dihydroxy carboxylic acids include dialkyrol alkanoic acids such as dimethylol alkanoic acids (eg, dimethylol acetic acid, dimethylol butanoic acid, dimethylol propionic acid, dimethylol butyric acid, dimethylol pentanoic acid). These may be one kind or a mixture of two or more kinds.

  The urethane resin may be obtained by further reacting with another polyol or chain extender in addition to the polyol and polyisocyanate. Examples of other polyols include sorbitol, 1,2,3,6-hexanetetraol, 1,4-sorbitan, 1,2,4-butanetriol, 1,2,5-pentanetriol, glycerin, trimethylol Polyols having 3 or more hydroxyl groups such as ethane, trimethylolpropane and pentaerythritol are included. Examples of other chain extenders include ethylene glycol, diethylene glycol, triethylene glycol, 1,3-propanediol, 1,3-butanediol, 1,4-butanediol, neopentyl glycol, pentanediol, 1,6 -Glycols such as hexanediol and propylene glycol; aliphatic diamines such as ethylenediamine, propylenediamine, hexamethylenediamine, 1,4-butanediamine, and aminoethylethanolamine; isophoronediamine, 4,4'-dicyclohexylmethanediamine, etc. Alicyclic diamines; aromatic diamines such as xylylenediamine and tolylenediamine are included.

  The number average molecular weight of the urethane resin is preferably 5,000 to 600,000, more preferably 10,000 to 400,000. The acid value of the urethane resin is preferably 10 or more, more preferably 10 to 50, and still more preferably 20 to 45. The resin layer containing a urethane resin having an acid value in the above range can improve the adhesion between the protective film and the polarizer.

  The specific resin layer may further contain fine particles as necessary. This is because the specific resin layer containing the fine particles can suppress blocking that tends to occur when the protective film is wound.

  As examples of the fine particles contained in the specific resin layer, the same fine particles (mat agent) that can be contained in the transparent polymer substrate layer can be used. The fine particles are preferably contained in at least one of the transparent polymer substrate layer and the specific resin layer, and more preferably contained in the specific resin layer.

  The content of the fine particles (solid content) is preferably 0.3 to 10 parts by weight with respect to 100 parts by weight of the urethane resin (solid content; if the cross-linking agent is included, the solid content including the cross-linking agent), More preferably, it is 0.6-3 weight part. If the content of the fine particles is less than 0.3 parts by weight, the unevenness cannot be sufficiently formed on the surface of the specific resin layer, so that it is difficult to obtain a blocking inhibiting effect. On the other hand, when the content of the fine particles exceeds 10 parts by weight, the haze of the protective film having a specific resin layer can be easily increased.

  The thickness of the specific resin layer is preferably 0.1 to 10 μm, more preferably 0.1 to 5 μm, and further preferably 0.2 to 1.5 μm. When the thickness of the specific resin layer is more than 10 μm, a phase difference may appear in the specific resin layer, and when it is less than 0.1 μm, it is difficult to obtain sufficient adhesion between the polarizer and the protective film. .

  The protective film having a specific resin layer may further have other functional layers (an adhesive layer, a dye layer, an antistatic layer, an antihalation layer, a UV absorption layer, a polarizing layer, etc.) as necessary.

  A protective film having a specific resin layer is a polarizing plate protective film for liquid crystal display devices, a retardation film, an antireflection film, a brightness enhancement film, a hard coat film, an antiglare film, an antistatic film, and optical compensation for widening the viewing angle. Used as a film.

Method for Producing Protective Film Having Specific Resin Layer A protective film having a specific resin layer is formed on the above-mentioned transparent polymer base material layer with a specific resin layer composition (also simply referred to as “resin layer composition”). Can be obtained by drying.

  The resin layer composition includes the above-described resin, and may further include fine particles, a crosslinking agent or an additive, which will be described later, as necessary.

  When the resin contained in the composition is a urethane resin having a carboxyl group, the crosslinking agent contained in the resin layer composition is preferably a polymer having a group capable of reacting with a carboxyl group. Examples of the group capable of reacting with a carboxyl group include an organic amino group, an oxazoline group, an epoxy group, a carbodiimide group, and the like, preferably an oxazoline group. This is because a cross-linking agent having an oxazoline group has a long pot life at room temperature when mixed with a urethane resin, and a cross-linking reaction easily proceeds by heating.

  Examples of the polymer having a group capable of reacting with a carboxyl group include an acrylic polymer and a styrene / acrylic polymer, and an acrylic polymer is preferable. The acrylic polymer can enhance the adhesion between the specific resin layer containing the polymer and the polarizer. In addition, the acrylic polymer is well compatible in the aqueous resin layer composition described below, and can cross-link the urethane resin well.

  Examples of the additive contained in the resin layer composition include an antiblocking agent, a dispersion stabilizer, a thixotropic agent, an antioxidant, an ultraviolet absorber, an antifoaming agent, a thickener, a dispersant, a surfactant, Catalysts, fillers, lubricants, antistatic agents, organosilane compounds (epoxy group-containing silane coupling agents, amino group-containing silane coupling agents, silane coupling agents such as isocyanate group-containing silane coupling agents) and the like are included.

  The resin layer composition is preferably aqueous. The content of the urethane resin in the resin layer composition is preferably 1.5 to 15% by weight, more preferably 2 to 2% so that the viscosity of the resin layer composition can be uniformly applied. 10% by weight.

  The content of the crosslinking agent (solid content) in the resin layer composition is preferably 1 to 30 parts by weight, more preferably 3 to 20 parts by weight with respect to 100 parts by weight of the urethane resin (solid content). . When the content of the crosslinking agent is less than 1 part by weight, it is difficult to obtain sufficient adhesion with the polarizer. On the other hand, when the content of the crosslinking agent is more than 30 parts by weight, a phase difference may appear in a specific resin layer.

  Examples of the method for applying the resin layer composition may include a bar coating method, a roll coating method, a gravure coating method, a rod coating method, a slot orifice coating method, a curtain coating method, and a fountain coating method. The drying temperature can be 50 ° C. or higher, preferably 90 ° C. or higher, more preferably 110 ° C. or higher. The drying temperature is preferably 200 ° C. or lower, more preferably 180 ° C. or lower. This is because when the drying temperature is within the above range, the resulting polarizing plate has high color resistance (particularly color resistance under high temperature and high humidity).

Other protective films Protective films (other protective films) other than the protective film having a specific resin layer are not particularly limited as long as they are transparent resin films, and are preferably thermoplastic resin films. A preferable example of such a thermoplastic resin film includes a cellulose ester film.

  The cellulose ester film is not particularly limited, and may be a film containing the aforementioned cellulose ester or a commercially available cellulose ester film. Examples of commercially available products include cellulose ester films (for example, Konica Minoltak KC8UX, KC4UX, KC5UX, KC8UY, KC4UY, KC12UR, KC8UCR-3, KC8UCR-4, KC8UCR-5, KC8UE, KC4FR, KC4FR-3, CC4FR-3 4, KC4HR-1, KC8UY-HA, KC8UX-RHA, manufactured by Konica Minolta Opto Co., Ltd.) and the like.

  The thickness of the other protective film is not particularly limited, but can be about 10 to 200 μm, preferably 10 to 100 μm, and more preferably 10 to 70 μm.

  As described above, the polarizing plate includes a polarizer and a protective film disposed on at least one surface thereof.

  The polarizers (the first polarizer 42 and the second polarizer 62) are elements that allow only light having a polarization plane in a certain direction to pass therethrough. A typical example of the polarizer is a polyvinyl alcohol-based polarizing film, and there are one in which a polyvinyl alcohol-based film is dyed with iodine and one in which a dichroic dye is dyed.

  The polarizer may be a film obtained by uniaxially stretching a polyvinyl alcohol film and then dyeing with iodine or a dichroic dye, or after dyeing a polyvinyl alcohol film with iodine or a dichroic dye, A uniaxially stretched film (preferably a film further subjected to durability treatment with a boron compound) may be used. The thickness of the polarizer is preferably 5 to 30 μm, and more preferably 10 to 20 μm.

  The polyvinyl alcohol film may be a film formed from a polyvinyl alcohol aqueous solution. The polyvinyl alcohol film is preferably an ethylene-modified polyvinyl alcohol film because it is excellent in polarizing performance and durability performance and has few color spots. Examples of the ethylene-modified polyvinyl alcohol film include an ethylene unit content of 1 to 4 mol%, a polymerization degree of 2000 to 4000, and a saponification degree of 99 described in JP2003-248123A, JP2003-342322A, and the like. 0.0 to 99.99 mol% film is included.

  Examples of dichroic dyes include azo dyes, stilbene dyes, pyrazolone dyes, triphenylmethane dyes, quinoline dyes, oxazine dyes, thiazine dyes and anthraquinone dyes.

  A polarizing plate can be obtained by bonding a polarizer and the above-described protective films (F1 to F4) through an adhesive. For example, in the second polarizing plate 60, the protective film F3 is bonded to one surface of the second polarizer 62 with an adhesive, and the protective film F4 is bonded to the other surface of the second polarizer 62. And a step of bonding through an adhesive.

  It is preferable that the adhesive used for bonding at least the protective film F3 and the polarizer described above is a photocurable adhesive. That is, it is preferable that an adhesive layer made of a photocurable adhesive is disposed between the specific resin layer of the protective film F3 and the second polarizer 62. A photocurable adhesive agent can improve the adhesiveness of a polarizer and the protective film F3. In addition, the adhesive layer made of a photo-curable adhesive has a higher elastic modulus than conventional polyvinyl alcohol adhesives, making it difficult to transmit the dimensional change force of the polarizer to the liquid crystal cell and making the liquid crystal panel less likely to warp. sell.

About Photocurable Adhesive The photocurable adhesive contains a photocurable compound, and may further contain a crosslinking agent, a photopolymerization initiator, other additives and the like as necessary.

  The photocurable resin can be an ultraviolet curable resin or an electron beam curable resin. The ultraviolet curable resin may be a radical polymerizable resin or a cationic polymerizable resin. The ultraviolet curable resin may be one kind or a mixture of two or more kinds. The mixture of two or more types may be a mixture of two or more types of radical polymerizable resins, may be a mixture of two or more types of cationic polymerizable resins, or a radical polymerizable resin and a cationic polymerizable resin. It may be a mixture of

  Examples of the radical polymerizable resin include (meth) acrylic resin, (meth) acrylamide resin, and the like. The (meth) acrylic resin is the same as described above. Examples of (meth) acrylamide resins include N-methyl (meth) acrylamide, N, N-dimethyl (meth) acrylamide, N-isopropylacrylamide, N-methylol (meth) acrylamide, aminomethyl (meth) acrylamide, aminoethyl (Meth) acrylamide, N-hydroxyethyl (meth) acrylamide, N- (2,2-dimethoxy-1-hydroxyethyl)-(meth) acrylamide, N-hydroxymethyl (meth) acrylamide, p-hydroxyphenyl (meth) Acrylamide and the like are included, and N-hydroxyethyl (meth) acrylamide is preferable.

  Examples of the cationic polymerizable resin include an epoxy resin. The epoxy resin can be a bifunctional or higher aromatic epoxy resin or an aliphatic epoxy resin. Examples of aromatic epoxy resins include bisphenol-type epoxy resins such as diglycidyl ether of bisphenol A, diglycidyl ether of bisphenol F, diglycidyl ether of bisphenol S; novolak type such as phenol novolac epoxy resin and cresol novolac epoxy resin Epoxy resins thereof; hydrides thereof and the like. Examples of the aliphatic epoxy resin include diglycidyl ethers such as 1,4-butanediol and 1,6-hexanediol, and triglycidyl ethers of glycerin. The epoxy resin can be a monomer, oligomer, polymer, or a mixture thereof.

  Among these, an epoxy resin is preferable because it is easy to handle and has high adhesive strength.

  It is preferable that the photocurable adhesive (ultraviolet curable adhesive) containing an ultraviolet curable resin further contains a photopolymerization initiator. The photopolymerization initiator can be a photoradical polymerization initiator or a photocationic polymerization initiator.

  Content of a photoinitiator is about 0.1-10 weight part normally per 100 weight part of curable resin, Preferably it is 0.5-3 weight part. On the other hand, the photocurable adhesive (electron beam curable adhesive) containing an electron beam curable resin does not necessarily need to contain a photopolymerization initiator.

  The photocurable adhesive may further contain an additive as necessary. Examples of such additives include sensitizers (for example, carbonyl compounds) for increasing the curing rate and sensitivity by electron beams, adhesion promoters (for example, silane coupling agents and ethylene oxide), and specific resin layers of protective films. Additives that improve wettability, additives that improve the mechanical strength and processability of the adhesive layer (eg acryloxy group compounds, hydrocarbon natural resins or synthetic resins), UV absorbers, anti-aging agents, dyes , Processing aids, ion trapping agents, antioxidants, tackifiers, fillers (other than metal compound fillers), plasticizers, leveling agents, foaming inhibitors, antistatic cracks, and the like.

  The thickness of the adhesive layer obtained from the photocurable adhesive is preferably 0.01 to 10 μm, more preferably 0.01 to 5 μm. When the thickness of the adhesive layer is less than 0.01 μm, it is difficult to obtain sufficient adhesive strength, and when the thickness of the adhesive layer exceeds 10 μm, not only the transparency of the adhesive layer is easily impaired, Peeling is likely to occur, and the resulting polarizing plate may not have sufficient durability.

  The polarizing plate including at least the protective film F3 is a step of bonding the protective film F3 and the polarizer through a photocurable adhesive; an active energy ray (on the laminate including the bonded polarizer and the protective film F3). And a step of photocuring the adhesive layer obtained from the photocurable adhesive.

  In the step of bonding the protective film F3 and the polarizer through the photocurable adhesive, at least one of the surface of the polarizer to which the protective film F3 is bonded and the surface of the specific resin layer of the protective film F3 is photocured. An adhesive layer may be formed by applying a functional adhesive. As described above, it is important that at least the protective film F3 has a specific resin layer.

  The coating method of the photocurable adhesive can be selected depending on the viscosity and coating thickness of the photocurable adhesive. Examples of the application method of the photocurable adhesive include a reverse coater, a gravure coater (direct, reverse and offset), a bar reverse coater, a roll coater, a die coater, a bar coater, a rod coater, and the like.

  Bonding of the polarizer and the specific resin layer of the protective film can be performed with a roll laminator or the like.

  An active energy ray (electron beam, ultraviolet ray, etc.) is irradiated to the laminated body of the polarizer and protective film bonded together through the photocurable adhesive agent, and an adhesive layer is hardened. Irradiation of active energy rays can be performed from any direction, and it is preferable to irradiate from the outside of the protective film. When the active energy ray is irradiated from the polarizer side, the polarizer may be deteriorated by the active energy ray.

When curing the adhesive layer obtained from the ultraviolet curable adhesive, irradiation of ultraviolet rays is preferably 100 to 500 mJ / cm ² in accumulated light quantity, and more preferably 200 to 400 mJ / cm ^2.

  When the adhesive layer obtained from the electron beam curable adhesive is cured, the electron beam irradiation has an acceleration voltage of preferably 5 to 300 kV, more preferably 10 to 250 kV. When the acceleration voltage is less than 5 kV, the electron beam cannot be sufficiently irradiated in the thickness direction of the adhesive layer, and the curing tends to be insufficient. On the other hand, when the acceleration voltage exceeds 300 kV, the protective film and the polarizer are easily damaged by the electron beam. The irradiation dose of the electron beam is preferably 5 to 100 kGy, more preferably 10 to 75 kGy. When the irradiation dose is less than 5 kGy, the adhesive layer tends to be insufficiently cured, and when it exceeds 100 kGy, the protective film and the polarizer are damaged, and mechanical strength is lowered and yellowing is likely to occur.

  The electron beam irradiation is usually performed in an inert gas atmosphere, but may be performed in the air or in an atmosphere containing a small amount of oxygen if necessary.

  When the polarizing plate is continuously produced in a line, the line speed is preferably 1 to 500 m / min, more preferably 5 to 300 m / min, and still more preferably 10 although it depends on the curing time of the photocurable adhesive. It can be set to ˜100 m / min. If the line speed is too low, productivity is low and damage to the protective film tends to increase. On the other hand, if the line speed is too high, the photocurable adhesive is not sufficiently cured, and it is difficult to obtain sufficient adhesiveness.

Polyvinyl alcohol-based adhesive The adhesive used for bonding the other protective film and the polarizer is not particularly limited, and may be the above-described photo-curable adhesive or polyvinyl alcohol-based adhesive. May be.

  The polyvinyl alcohol-based adhesive includes a resin such as a polyvinyl alcohol resin and an acetoacetyl group-containing polyvinyl alcohol resin, and may further include a crosslinking agent as necessary.

  Examples of polyvinyl alcohol resins include saponified products of polyvinyl acetate or derivatives thereof; saponified products of copolymers of vinyl acetate and copolymer components; acetalized, urethanized, etherified, grafted or phosphorylated with polyvinyl alcohol. Examples include acid esterified modified polyvinyl alcohol. Examples of copolymer components include unsaturated carboxylic acids such as (anhydrous) maleic acid, fumaric acid, crotonic acid, itaconic acid, (meth) acrylic acid and esters thereof; α-olefins such as ethylene and propylene; ) Allyl sulfonic acid (soda), sulfonic acid soda (monoalkyl malate), disulfonic acid soda alkyl maleate, N-methylol acrylamide, acrylamide alkyl sulfonic acid alkali salt, N-vinyl pyrrolidone, N-vinyl pyrrolidone derivatives, etc. It is. These resins may be one kind or a mixture of two or more kinds.

  The average degree of polymerization of the polyvinyl alcohol-based resin is preferably about 100 to 5000, and more preferably 1000 to 4000, from the viewpoint of adhesiveness. The average saponification degree is preferably about 85 to 100 mol%, more preferably 90 to 100 mol% from the viewpoint of adhesiveness.

  The acetoacetyl group-containing polyvinyl alcohol resin is obtained by reacting a polyvinyl alcohol resin with diketene. An acetoacetyl group-containing polyvinyl alcohol resin is a method in which diketene is added to a dispersion obtained by dispersing a polyvinyl alcohol resin in a solvent such as acetic acid; a polyvinyl alcohol resin is dissolved in a solvent such as dimethylformamide or dioxane. It can be obtained by adding diketene to the resulting solution; or by directly contacting diketene gas or liquid diketene with a polyvinyl alcohol resin.

  The degree of acetoacetyl group modification of the acetoacetyl group-containing polyvinyl alcohol resin is 0.1 mol% or more, preferably about 0.1 to 40 mol%, more preferably 1 to 20%, and still more preferably. Is 2-7 mol%. When the degree of acetoacetyl group modification is less than 0.1 mol%, the resulting adhesive layer tends to have insufficient water resistance, and when the degree of acetoacetyl group modification exceeds 40 mol%, the effect of increasing water resistance is sufficient. It may not be. The degree of acetoacetyl group modification of the acetoacetyl group-containing polyvinyl alcohol resin can be measured by NMR.

  Examples of the crosslinking agent contained in the polyvinyl alcohol-based adhesive may be a compound having at least two functional groups having reactivity with the polyvinyl alcohol-based resin. Specific examples thereof include ethylenediamine, triethylenediamine, hexamethylene. Alkylene diamines having two amino groups and an alkylene group such as diamine; tolylene diisocyanate, hydrogenated tolylene diisocyanate, trimethylolpropane tolylene diisocyanate adduct, triphenylmethane triisocyanate, methylenebis (4-phenylmethane triisocyanate, isophorone Diisocyanates and isocyanates such as ketoxime block products or phenol block products; ethylene glycol diglycidyl ether, polyethylene glycol diglycidyl Epoxys such as ether, glycerin di or triglycidyl ether, 1,6-hexanediol diglycidyl ether, trimethylolpropane triglycidyl ether, diglycidyl aniline, diglycidyl amine; monomers such as formaldehyde, acetaldehyde, propionaldehyde, butyraldehyde Aldehydes: Glyoxal, malondialdehyde, succindialdehyde, glutardialdehyde, maleidialdehyde, phthaldialdehyde and other dialdehydes; methylol urea, methylol melamine, alkylated methylol urea, alkylated methylolated melamine, acetoguanamine, Amino-formaldehyde resins such as condensates of benzoguanamine and formaldehyde; sodium, potassium, magnesi And divalent metals such as calcium, aluminum, iron, nickel, etc., salts of trivalent metals and their oxides, etc. Among them, amino-formaldehyde resins and dialdehydes are preferred. The dialdehyde is preferably glyoxal, preferably a compound having a methylol group, and particularly preferably methylol melamine.

  The content of the crosslinking agent in the polyvinyl alcohol-based adhesive is about 10 to 60 parts by weight, preferably 20 to 50 parts by weight with respect to 100 parts by weight of the polyvinyl alcohol-based resin. This is because an adhesive having a polyvinyl alcohol-based resin content in the above range has high adhesiveness. If the content of the crosslinking agent is more than 60 parts by weight, the reaction of the crosslinking agent is likely to proceed in a short time and the adhesive is easily gelled, so that the pot life is likely to be shortened.

  The polyvinyl alcohol-based adhesive may contain a metal compound colloid as necessary. The metal compound colloid is one in which metal compound fine particles are dispersed in a dispersion medium, and may have stability. A polyvinyl alcohol adhesive containing a metal compound colloid is relatively stable even if the content of the crosslinking agent is large.

  The average particle size of the metal compound colloid fine particles is preferably 1 to 100 nm, more preferably 1 to 50 nm. Since the fine particles of the metal compound colloid can be uniformly dispersed in the adhesive layer, knick defects (light leakage) can be suppressed while ensuring adhesion.

  Examples of metal compounds constituting the metal compound colloid include metal oxides such as alumina, silica, zirconia, and titania; metal salts such as aluminum silicate, calcium carbonate, magnesium silicate, zinc carbonate, barium carbonate, and calcium phosphate; celite , Minerals such as talc, clay and kaolin. Among these, a metal compound having a positive charge is preferable. Examples of such a metal compound include silica, alumina, titania, and the like, and silica and alumina are preferable.

  The metal compound colloid exists in the state of a colloid solution dispersed in a dispersion medium. Examples of the dispersion medium include water and alcohols. The solid content concentration in the colloidal solution is about 1 to 50% by weight, preferably 1 to 30% by weight. The metal compound colloid may further contain an acid such as nitric acid, hydrochloric acid, and acetic acid as a stabilizer.

  The content of the metal compound colloid (solid content) in the polyvinyl alcohol adhesive is preferably 200 parts by weight or less, preferably 10 to 200 parts by weight, more preferably 100 parts by weight of the polyvinyl alcohol resin. 20 to 175 parts by weight, particularly preferably 30 to 150 parts by weight. When the content of the metal compound colloid is within the above range, the fine particles of the metal compound colloid can be uniformly dispersed in the adhesive layer, so that knick defects (light leakage) can be suppressed while ensuring adhesiveness.

  The polyvinyl alcohol-based adhesive further includes a coupling agent such as a silane coupling agent and a titanium coupling agent, a tackifier, an ultraviolet absorber, an antioxidant, a heat stabilizer, and a hydrolysis stabilizer as required. May include.

  The polyvinyl alcohol-based adhesive is preferably an aqueous solution (aqueous resin solution). The resin concentration of the polyvinyl alcohol-based adhesive is preferably from 0.1 to 15% by weight, more preferably from 0.5 to 10% by weight, from the viewpoint of improving the coatability and storage stability. The viscosity of the resin solution is preferably 1 to 50 mPa · s. The viscosity of the polyvinyl alcohol-based adhesive containing the metal compound colloid can be about 1 to 20 mPa · s. The pH of the resin solution is preferably 2 to 6, more preferably 2.5 to 5, particularly preferably 3 to 5, and most preferably 3.5 to 4.5. The surface charge of the metal compound colloid can usually be adjusted by pH. The surface charge of the metal compound colloid is preferably a positive charge. By having a positive charge, generation of nick defects can be further suppressed. The surface charge of the metal compound colloid can be confirmed, for example, by measuring the zeta potential with a zeta potential measuring device.

  The polyvinyl alcohol-based adhesive containing a cross-linking agent and a metal compound colloid is, for example, a method of blending a metal compound colloid in a solution prepared by mixing a polyvinyl alcohol-based resin and a cross-linking agent in advance and adjusting to an appropriate concentration; After mixing resin and metal compound colloid, it can prepare by the method of mixing a crosslinking agent.

  The thickness of the adhesive layer obtained from the polyvinyl alcohol-based adhesive is preferably 10 to 300 nm, more preferably 10 to 200 nm, and particularly preferably 20 to 150 nm. If the thickness of the adhesive layer is within the above range, sufficient adhesiveness can be easily obtained.

  The polarizing plate including the other transparent protective film includes a step of bonding the other protective film and the polarizer through a polyvinyl alcohol-based adhesive; and a step of drying the laminate of the bonded polarizer and the protective film. It can be obtained through.

  The application method of the polyvinyl alcohol-based adhesive can be, for example, a roll method, a spray method, an immersion method, or the like. Moreover, when a polyvinyl alcohol-type adhesive agent contains a metal compound colloid, as for the application | coating thickness of a polyvinyl alcohol-type adhesive agent, the thickness after drying is made larger than the average particle diameter of a metal compound colloid. The drying temperature can be 5 to 150 ° C, preferably 30 to 120 ° C. The drying time can be 120 seconds or longer, preferably 300 seconds or longer.

  The backlight 80 may be a sidelight (edge light) type surface light source in which a known light source is disposed on the side of the light guide plate, or a direct type surface light source in which a known light source is arranged under the diffusion plate. Examples of known light sources include cold cathode fluorescent lamps (CCFL), hot cathode fluorescent lamps (HCFL), external electrode fluorescent lamps (EEFL), flat fluorescent lamps (FFL), light emitting diode elements (LEDs), organic electroluminescent elements (OLEDs). ) Is included.

  Among these, from the viewpoint of reducing the power consumption of the liquid crystal display device, a backlight using an LED as a light source (LED backlight) is preferable.

  Since the liquid crystal display device having the LED backlight is thin, the distance between the liquid crystal cell 20 and the first and second polarizing plates 40 and 60 disposed on both sides thereof and the LED backlight 80 is extremely small. For this reason, the warpage of the liquid crystal cell is likely to occur significantly due to the heat of the LED backlight.

  The liquid crystal display device of the present invention includes at least a “protective film having a specific resin layer” as the protective film F3. Even if the protective film having a specific resin layer is not subjected to a surface treatment such as a corona treatment, a plasma treatment, or a saponification treatment, the protective film can be favorably bonded to the polarizer. Thereby, the adhesion nonuniformity of the protective film and polarizer resulting from surface treatment can be reduced. Furthermore, the liquid crystal display device of the present invention has “an adhesive layer obtained from a photocurable adhesive” between at least the protective film F3 and the polarizer (second polarizer 62). Thereby, the curvature of a liquid crystal panel can be reduced, further improving the adhesiveness of a polarizer and a protective film.

  Therefore, display unevenness of a liquid crystal display device; in particular, display unevenness that is conspicuous in a liquid crystal display device having a high aperture ratio, a liquid crystal display device having a COA structure, a liquid crystal display device having an LED backlight, and the like can be suppressed.

  In the following, the invention will be described in more detail with reference to examples. These examples do not limit the scope of the present invention.

1. Preparation of materials 1) Transparent polymer substrate Acrylic resin film LMMA: Lactonized polymethyl methacrylate film (Lactonization rate 20%, no UV absorber, R _{0 at} wavelength 590 nm: 0 μm, Rth: 0 nm, thickness 30 μm)
Norbornene-based resin film ZEONOR1: manufactured by Nippon Zeon Co., Ltd., trade name: ZEONOR (no UV absorber, R ₀ at a wavelength of 590 nm: 70 μm, Rth: 250 nm, thickness: 40 μm)
ZEONOR2: manufactured by Nippon Zeon Co., Ltd., trade name: ZEONOR (no UV absorber, R ₀ at a wavelength of 590 nm: 0 μm, Rth: 0 nm, thickness: 40 μm)
ZEONOR3: manufactured by Nippon Zeon Co., Ltd., trade name: ZEONOR (no UV absorber, R _{0 at} wavelength 590 nm: 52 μm, Rth: 125 nm, thickness 40 μm)
Cellulose ester film (cellulose triacetate film)
KC4CZ: manufactured by Konica Minolta Opto, Inc., trade name: KC4CZ (no UV absorber, R ₀ at a wavelength of 590 nm: 0 μm, Rth: 0 nm, thickness: 40 μm)
KC4UA: manufactured by Konica Minolta Opto, trade name: KC4UA (with UV absorber, thickness 40 μm)

2) Specific resin layer composition (Synthesis Example 2-1)
Polyester urethane (Daiichi Kogyo Seiyaku Co., Ltd., trade name: Superflex 210, solid content 33%) 16.8 g, cross-linking agent (oxazoline-containing polymer, product of Nippon Shokubai Co., Ltd., trade name: Epocross WS-700, solid content 25% ) 4.2 g, 2.0 g of 1 wt% ammonia water, 0.42 g of colloidal silica (manufactured by Fuso Chemical Industries, trade name: Quattron PL-3, solid content 20 wt%) and 76.6 g of pure water are mixed. Resin layer composition 1 was obtained.

(Synthesis Example 2-2)
Synthesis Example 1 except that the polyester urethane (Daiichi Kogyo Seiyaku Co., Ltd., trade name: Superflex 210, solid content 33%) is changed to polyether urethane (Dainippon Ink & Chemicals, trade name: Hydran WLS202). In the same manner as above, a resin layer composition 2 was obtained.

(Synthesis Example 2-3)
Polyester urethane (Daiichi Kogyo Seiyaku Co., Ltd., trade name: Superflex 210, solid content 33%) 17.0 g, crosslinking agent (oxazoline-containing polymer, Nippon Shokubai Co., Ltd., trade name: Epocross WS-700, solid content 25% ) 4.2 g and 78.6 g of pure water were mixed to obtain a resin layer composition 3.

3) Composition for adhesive layer (Synthesis Example 3-1)
3 parts by weight of a photopolymerization initiator (manufactured by Ciba Japan, trade name: Irgacure 127) was blended with 100 parts by weight of N-hydroxyethylacrylamide to obtain Composition 1 for an adhesive layer.

(Synthesis Example 3-2)
10.0 g of hydrogenated epoxy resin (diglycidyl ether of bisphenol A, manufactured by Japan Epoxy Resin, trade name: Epicoat YX8000) is mixed with 4.0 g of a photopolymerization initiator (trade name: SP-500, manufactured by ADEKA). Thus, an adhesive composition 2 was obtained.

(Synthesis Example 3-3)
100 parts by weight of an acetoacetyl group-containing polyvinyl alcohol resin (average polymerization degree 1200, saponification degree 98.5 mol%, acetoacetyl group modification degree 5 mol%) and 20 parts by weight of methylol melamine are purified at 30 ° C. To obtain an aqueous solution having a solid content concentration of 0.5%. Thereby, the composition 3 for contact bonding layers was obtained.

Example 1
Production of Polarizer A polyvinyl alcohol film having an average polymerization degree of 2400, a saponification degree of 99.9 mol%, and a thickness of 75 μm was immersed in warm water at 30 ° C. for 60 seconds to swell. While the obtained film is dyed for 1 minute in an iodine solution of 0.3 wt% (weight ratio: iodine / potassium iodide = 0.5 / 8) at 30 ° C., the draw ratio becomes 3.5 times. Until it was stretched in a certain direction. The obtained film was stretched while being immersed in a 4% by weight boric acid aqueous solution at 65 ° C. for 0.5 minutes until the total stretch ratio in the above-mentioned fixed direction was 6 times. After stretching, the obtained film was dried in an oven at 70 ° C. for 3 minutes to obtain a polarizer having a thickness of 26 μm. The water content of the polarizer was 13.5% by weight.

Preparation of first polarizing plate (viewing side polarizing plate) KC4UA (cellulose ester film) was prepared. KC4UA (cellulose ester film) was immersed in a 2 mol / L sodium hydroxide solution at 60 ° C. for 90 seconds, then washed with water and dried to obtain a saponified cellulose ester film as protective film F1.

On the other hand, ZEONOR1 (norbornene resin film) was prepared as a transparent polymer substrate layer. One side of ZEONOR1 (norbornene resin film) was subjected to corona discharge treatment. The electron irradiation amount in the corona discharge was 77 W / m ² / min. On the corona-treated surface of the obtained film, the resin layer composition 3 was applied with a bar coater so that the thickness after drying was 0.3 μm, and then dried at 150 ° C. to form a specific resin layer. did. Thereby, the protective film F2 which has a transparent polymer base material layer and a specific resin layer was obtained.

  After applying the adhesive composition 3 on both sides of the polarizer so that the thickness after drying is 0.05 μm, the protective film F2 is provided on one side of the polarizer and the protective film F1 is provided on the other side. The laminate was obtained by bonding. The obtained laminate was subjected to thermocompression bonding using a small laminator and then dried for 5 minutes with a hot air dryer (70 ° C.) to obtain a first polarizing plate (viewing-side polarizing plate).

Production of Second Polarizing Plate (Backlight Side Polarizing Plate) LMMA (Lactonized polymethyl methacrylate film) was prepared as a transparent polymer substrate layer. A resin layer composition 1 was applied on one side of LMMA (lactonized polymethyl methacrylate film) with a bar coater so that the thickness after drying was 0.3 μm, and then dried at 140 ° C. to be a specific resin layer. Formed. Thereby, the protective film F3 which has a transparent polymer base material layer and a specific resin layer was obtained. Similarly, protective film F4 was obtained.

  Furthermore, on the specific resin layers of the protective films 3 and 4, the composition 1 for the adhesive layer was respectively cured with a microgravure coater (gravure roll: # 300, rotational speed 140% / line speed), and the thickness after curing was 5 μm. It applied so that it might become, and protective films F3 and F4 with an adhesive were obtained.

Protective films F3 and F4 with an adhesive were bonded to both surfaces of the polarizer by a roll machine, respectively. Thereafter, each of the protective films F3 and F4 was irradiated with ultraviolet rays to cure the adhesive. The line speed was 20 m / min, and the cumulative amount of ultraviolet light applied to the protective films F3 and F4 was 200 mJ / cm ² , respectively. Thus, a second polarizing plate (backlight-side polarizing plate) was obtained.

Production of Liquid Crystal Display Device A liquid crystal cell shown in FIGS. 2 and 3 (a liquid crystal cell shown in FIG. 16 of JP2009-301010A) was prepared. In this liquid crystal cell, a thin film transistor and a color filter are arranged on the same substrate. The above-mentioned first polarizing plate was bonded to the surface on the viewing side of the obtained liquid crystal cell, and the above-mentioned second polarizing plate was bonded to the surface on the backlight side. The first polarizing plate is bonded so that the protective film F2 is disposed on the surface of the polarizer on the liquid crystal cell side, and the second polarizing plate is disposed on the surface of the polarizer on the liquid crystal cell side with the protective film F3. I stuck together. Furthermore, an LED backlight unit manufactured by SONY BRAVIA KDL-46HX800) was used. Thereby, a liquid crystal display device having an aperture ratio of 67% was obtained.

(Examples 2 to 7)
As shown in Table 1, liquid crystal was obtained in the same manner as in Example 1 except that the types of the protective films F1 to F4, the presence or absence of the surface treatment, the presence or absence of the specific resin layer, or the type of adhesive were changed. A display device was obtained.

(Comparative Examples 1-7)
As shown in Table 1, liquid crystal was obtained in the same manner as in Example 1 except that the types of the protective films F1 to F4, the presence or absence of the surface treatment, the presence or absence of the specific resin layer, or the type of adhesive were changed. A display device was obtained.

Table 1 shows the configurations of the liquid crystal display devices obtained in Examples 1 to 7 and Comparative Examples 1 to 7.

Evaluation of display unevenness of liquid crystal display device The obtained liquid crystal display device was wet-heat treated for 24 hours in an environment of 23 ° C and 55% RH. Then, after 2 hours have passed since the backlight was turned on, the maximum luminance and the minimum luminance when displaying black were measured using a luminance distribution measuring device (trade name “CA-1500” manufactured by Konica Minolta). did. The maximum luminance and the minimum luminance were measured as follows. That is, the display screen of the liquid crystal panel was divided into a total of 16 sections of 4 horizontal sections × 4 vertical sections. Then, the lowest luminance among the luminances of the total of four sections, ie, the two central sections in the vertical direction and the two central sections in the horizontal direction, is set as the minimum luminance;

The black luminance ratio was calculated by dividing the obtained maximum luminance by the minimum luminance.
Black luminance ratio = maximum luminance / minimum luminance

Display unevenness was evaluated based on the following criteria.
◎: Less than 1.50 ○: 1.50 or more and less than 1.75 Δ: 1.75 or more and less than 2.00 ×: 2.00 or more

  On the other hand, the obtained liquid crystal display device was wet-heat treated for 24 hours in an environment of 50 ° C. and 90% RH. Thereafter, the black luminance ratio was measured in the same manner as described above to evaluate display unevenness.

Table 2 shows the evaluation results of the liquid crystal display device.

  It is shown that the display devices of Examples 1 to 7 have less display unevenness and better image display characteristics than the display devices of Comparative Examples 1 to 7 even in an environment where the wet heat conditions fluctuate.

  In particular, from the comparison between Example 7 and Comparative Examples 1 and 6, the protective film F3 is a protective film having a specific resin layer (untreated) and obtained by using a photocurable adhesive. The apparatus uses the protective film F3 as a corona-treated protective film having a specific resin layer, and the display devices of Comparative Examples 1 and 2 obtained using water paste, and the protective film F3 has a specific resin layer. It can be seen that display unevenness is suppressed as compared with the display device of Comparative Example 7 obtained by using a protective film that is not (untreated) and using water paste.

  Further, from the comparison with Examples 2 and 6, both of the protective films F2 and F3 are used as protective films having a specific resin layer, and the display device of Example 6 obtained by using a photocurable adhesive is protected. It can be seen that display unevenness is further suppressed as compared with the display device of Example 2 obtained by using only the film F3 as a protective film having a specific resin layer and using a photocurable adhesive.

  The liquid crystal display device of the present invention has a high front contrast and can suppress display unevenness.

DESCRIPTION OF SYMBOLS 10 Liquid crystal display device 20 Liquid crystal cell 40 1st polarizing plate 42 1st polarizer 44 Protective film (F1)
46 Protective film (F2)
60 Second polarizing plate 62 Second polarizer 64 Protective film (F3)
66 Protection Film (F4)
80 backlight 100 array substrate 200 counter substrate 110, 210 insulating substrate 124a, 124b gate electrode 140 gate insulating film 154a, 154b island-like semiconductor 163, 165 first and second island-like ohmic contact members 173a, 173b source electrode 175a, 175b Drain electrode 180p Lower protective film 180q Upper protective film 185a, 185b Contact hole 191a, 191b Pixel electrode 225a Through-hole 227 Light-shielding member opening 220 Light-shielding member 230 Color filter 270 Common electrode 300 Liquid crystal layer 11, 21 Alignment film 31 Liquid crystal molecule

Claims (13)

A liquid crystal display device having a first polarizing plate, a liquid crystal cell, a second polarizing plate, and an LED backlight in this order,
The liquid crystal cell is disposed on the second polarizing plate side, an array substrate provided with a thin film transistor and a color filter, and a counter substrate disposed on the first polarizing plate side and facing the array substrate. A liquid crystal layer sandwiched between the array substrate and the counter substrate and containing liquid crystal molecules,
The second polarizing plate has a second polarizer, and a protective film F3 disposed between the second polarizer and the array substrate,
The protective film F3 includes a transparent polymer base layer and a thermoplastic resin that is disposed on the surface of the transparent polymer base layer on the second polarizer side and includes a polyether unit, a polyester unit, or a polyacryl unit. Including a resin layer,
A liquid crystal display device, wherein an adhesive layer containing a cured product of a photocurable resin is disposed between the resin layer of the protective film F3 and the second polarizer. The first polarizing plate includes a first polarizer and a protective film F2 disposed between the first polarizer and the counter substrate.
The protective film F2 includes a transparent polymer base layer and a thermoplastic resin that is disposed on the surface of the transparent polymer base layer on the first polarizer side and includes a polyether unit, a polyester unit, or a polyacryl unit. Including a resin layer,
The liquid crystal display device according to claim 1, wherein an adhesive layer containing a cured product of a photocurable resin is disposed between the resin layer of the protective film F <b> 2 and the first polarizer. The second polarizing plate further includes a protective film F4 disposed on the backlight side surface of the second polarizing plate,
The protective film F4 includes a transparent polymer base layer and a thermoplastic resin that is disposed on a surface of the transparent polymer base layer on the second polarizer side and includes a polyether unit, a polyester unit, or a polyacryl unit. Including a resin layer,
3. The liquid crystal display device according to claim 1, wherein an adhesive layer containing a cured product of a photocurable resin is disposed between the resin layer of the protective film F <b> 4 and the second polarizer.   The liquid crystal display device according to claim 1, wherein the transparent polymer base material layer includes cyclic polyolefin or (meth) acrylic resin.   The liquid crystal display device according to claim 1, wherein the thermoplastic resin contained in the resin layer is a urethane resin.   The liquid crystal display device according to claim 1, wherein the resin layer further includes fine particles.   The liquid crystal display device according to any one of claims 1 and 4 to 6, wherein the photocurable resin contained in the adhesive layer is an ultraviolet curable resin.   The liquid crystal display device according to any one of claims 1 and 4 to 7, wherein the photocurable resin contained in the adhesive layer is a (meth) acrylamide resin or an epoxy resin.   The thickness of the said transparent polymer base material layer is a liquid crystal display device as described in any one of Claim 1 and 4-8 which is 20-40 micrometers.   The liquid crystal display device according to claim 1, wherein the aperture ratio is 65% or more.   The liquid crystal cell aligns the liquid crystal molecules perpendicular to the surface of the array substrate when no voltage is applied, and aligns the liquid crystal molecules horizontally with respect to the surface of the array substrate when a voltage is applied. The liquid crystal display device according to any one of claims 1 to 10. The liquid crystal molecule is a liquid crystal molecule having a positive dielectric anisotropy, and the array substrate includes a pixel electrode and a counter electrode that drive the liquid crystal molecule. A liquid crystal display device according to 1.   The liquid crystal display device according to claim 1, wherein the liquid crystal cell is a FFS (Fringe Field Switching) driving method.

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