TWI585474B - Optical film and optical film manufacturing method, polarizing film and liquid crystal display device - Google Patents

Description

Optical film and optical film manufacturing method, polarizing plate and liquid crystal display device

The present invention relates to a method for producing an optical film and an optical film, a polarizing plate, and a liquid crystal display device.

Portable liquid crystal display devices such as smart phones or tablets are now widely used. Such portable liquid crystal display devices are intended to be thinner.

The liquid crystal display device has a liquid crystal cell and a pair of polarizing plates. The polarizing plate generally has a pair of polarizers and a pair of protective films. Therefore, as the thickness of the portable liquid crystal display device is reduced, it is also desired to form a thin film of the component protective film.

The protective film is usually made of an original film that is stretched through the film. The thin film protective film is effective for thinning the thickness of the original film; however, when the original film is thinned, wrinkles are likely to occur. Therefore, it is desirable not to thin the thickness of the original film, but to thin the protective film by increasing the stretching ratio.

For this, it has been proposed to include fibers such as TAC or DAC. The original film of the cellulose acetate is obtained by a solution film forming method; the original film is obtained by extending the optical film in one direction at a high magnification (Patent Documents 1 to 3). In addition, it is also proposed to obtain an original film obtained by a melt film formation method comprising a cellulose ester having a carbon number of 3 or more and a sulfhydryl group such as CAP or CAB, and an optical film obtained by biaxially stretching the original film at a high magnification ( Patent Document 4). Further, an optical film obtained by biaxially stretching an original film containing cellulose acetate and a phosphate-based plasticizer by a solution forming method is proposed (Patent Document 5).

[Previous Technical Literature] [Patent Literature]

[Patent Document 1] Japanese Patent Laid-Open Publication No. 2009-288259

[Patent Document 2] Japanese Patent Laid-Open Publication No. 2002-127244

[Patent Document 3] Japanese Laid-Open Patent Publication No. 2007-264110

[Patent Document 4] Japanese Patent No. 4834444

[Patent Document 5] Japanese Patent Laid-Open Publication No. 2008-3126

However, as shown in Patent Document 4, a resin such as CAP or CAB which is suitable for the melt film forming method has relatively high flexibility. Therefore, although the original film containing these resins can be stretched at a high magnification, there is a problem that the stretched film is easily cloudy.

Also, the original film containing such a soft resin A film obtained by stretching at a high magnification tends to have a high elongation at break and a low tensile modulus. When the roll body of the film having a low tensile modulus is stored in such a manner that the core is horizontally stored for a long period of time, especially when the film thickness of the film is small, the center portion of the film in the width direction is recessed due to its own weight. The problem is that the shape is easily deteriorated.

Further, a portable liquid crystal display device such as a smart phone or a tablet computer may become a high temperature when compared with a television or a notebook computer. Therefore, when a film having a high elongation at break is used as a protective film of a portable liquid crystal display device, it is easily stretched by the influence of heat or humidity such as a backlight, and there is a problem that heat wrinkles occur. Further, as in Patent Documents 1 to 3, even in a film which is stretched in one direction at a high magnification (or a film having a low elongation at break in only one direction in the film surface), there is a problem that heat wrinkles occur.

Further, the original film of Patent Document 5 obtained by the solution film forming method is insufficient in stretchability, and it is difficult to sufficiently increase the stretching ratio.

The present invention has been made in view of the above circumstances, and an object thereof is to provide an optical film which has less white turbidity, is less likely to generate heat wrinkles, and has less deterioration in winding shape when stored in a roll body. Further, it is an object of the invention to provide a liquid crystal display device comprising such an optical film and having high brightness.

[1] An optical film characterized by a cellulose ester having a thiol group having a total degree of substitution of 2.0 to 3.0 and having a fluorenyl group of all ethylene groups, a retardation axis direction in the plane of the film, and the aforementioned retardation axis The elongation at break at 25 ° C in the direction perpendicular to the direction is 1 to 10%, and the thickness is 15 to 35 μm.

[2] The optical film according to [1], wherein the haze value measured in accordance with JIS K-7136 is 0.5 or less.

[3] The optical film according to [1], wherein the optical film further contains an additive having a ring structure and a molecular weight of 10,000 or less.

[4] The optical film according to [3], wherein the additive has a ring structure included in the repeating unit, a non-aromatic ring structure or an aromatic ring structure, a polyester compound or a styrene compound, or a pentose structure. Or a furanose structure, and the aforementioned sucrose structure or furanose structure is a sugar ester compound containing a substituent of a non-aromatic ring structure or an aromatic ring structure.

[5] The optical film according to [3] or [4] wherein the ring structure is an aromatic ring.

[6] The optical film according to any one of [3], wherein the additive is a polyester compound having a molecular weight of 600 or more in an aromatic ring structure and a benzene having a molecular weight of 600 or more. A vinyl compound.

[7] The optical film according to any one of [3], wherein the content of the additive is 5 to 30% by mass based on the cellulose ester.

The optical film according to any one of [1], wherein the direction of the slow axis in the plane of the film is at least 23 ° C, 55% in a direction perpendicular to the direction of the slow axis. The tensile modulus under RH is 5.0 to 8.0 GPa.

[9] The optical film according to any one of [1] to [8] wherein the elongation at break in the direction of the slow axis in the plane of the film and the direction perpendicular to the direction of the slow axis are 25 ° C. 1~5%.

[10] The optical film according to any one of [1] to [9] wherein the retardation R ₀ (590) in the in-plane direction at a measurement wavelength of 590 nm at 23 ° C and 55% RH is 10 nm or less.

[11] A method for producing an optical film, comprising: preparing a cellulose ester having a thiol group having a total degree of substitution of 2.0 to 3.0, and all of the fluorenyl group is an acetamyl group, and having a molecular weight of 10,000 having a ring structure; The following steps of doping the solution of the additive, a step of casting the aforementioned doping solution onto the endless metal support, a step of peeling the film obtained by drying the doping solution obtained by the above-mentioned metal support, The peeled film is stretched at a stretching ratio of 1.3 to 4.0 times in two directions perpendicular to each other in the plane of the film to obtain an optical film having a thickness of 15 to 35 μm.

[12] The method for producing an optical film according to the above [11], wherein the additive is a polyester compound or a styrene compound having a ring structure of a non-aromatic ring structure or an aromatic ring structure, or has a methane A pyranose structure or a furanose structure, and the aforementioned porphyrin structure or furanose structure is a sugar ester compound having a substituent including a non-aromatic ring structure or an aromatic ring structure.

[13] The method for producing an optical film according to [11], wherein the ring structure is an aromatic ring.

The method for producing an optical film according to any one of the aspects of the present invention, wherein the additive is a polyester compound having a molecular weight of 600 or more and a molecular weight of 600 in an aromatic ring structure. The above styrene compound.

[15] The method for producing an optical film according to any one of [10], wherein the content of the additive is 5 to 30% by mass based on the cellulose ester.

[16] The method for producing an optical film according to any one of [10], wherein the optical film has a retardation R ₀ (590) in an in-plane direction at a measurement wavelength of 590 nm at 23 ° C and 55% RH. ) is 10 nm or less.

[17] A polarizing plate comprising the optical film of any one of [1] to [10].

[18] A liquid crystal display device comprising the optical film according to any one of [1] to [10].

[19] A liquid crystal display device comprising: a liquid crystal cell; a first polarizing plate having a first polarizer on a surface on which the liquid crystal cell is disposed; and a second surface disposed on the other surface of the liquid crystal cell a liquid crystal display device of a second polarizer of polarized light, characterized in that The first polarizing plate is an optical film having any one of [1] to [10] disposed on a surface opposite to the liquid crystal cell of the first polarizer, or The second polarizing plate is an optical film having any one of the items [1] to [10] disposed on a side opposite to the liquid crystal cell of the second polarizer.

According to the present invention, it is possible to provide an optical body which has less white turbidity, is hard to generate heat wrinkles, and has less deterioration in winding shape when stored in a roll body. film. It can provide a liquid crystal display device with high brightness.

10‧‧‧Liquid crystal display device

30‧‧‧Liquid Crystal Unit

50‧‧‧First polarizer

51‧‧‧First polarizer

53‧‧‧Protective film (F1)

55‧‧‧Protective film (F2)

70‧‧‧Second polarizer

71‧‧‧Second polarizer

73‧‧‧Protective film (F3)

75‧‧‧Protective film (F4)

90‧‧‧ Backlight

Fig. 1 is a schematic view showing an example of a basic configuration of a liquid crystal display device of the present invention.

The invention is described in detail below. In the present specification, the term "~" is used in the sense that the numerical values described before and after are used as the lower limit and the upper limit.

Optical film

The optical film of the present invention comprises a cellulose ester and an additive having a ring structure.

Cellulose ester

The glucose unit constituting the cellulose bond β -1,4 has a free hydroxyl group (hydroxyl group) at the 2, 3 and 6 positions. The cellulose ester is a polymer which is a part or all of one of these hydroxyl groups (hydroxyl groups). The total degree of substitution of the fluorenyl group means the proportion of the hydroxyl group (hydroxyl group) of the cellulose at the 2, 3 and 6 positions which is thiolated (100% thiolation to the degree of substitution 3).

The thiol group contained in the cellulose ester is as described later, and it is preferable to use all of the fluorenyl group in order to reduce the white turbidity of the film after stretching. Fiber The esters are preferably cellulose acetates in which all of the thiol groups are acetamidine groups.

The total degree of substitution of the thiol group of the cellulose ester is preferably from 2.0 to 3.0, more preferably from 2.5 to 2.95, even more preferably from 2.55 to 2.95. It is impossible to form a film with a total degree of substitution of a fluorenyl group of 2.5 or more, and a cellulose ester having a fluorenyl group of all ethylene groups is formed by a melt casting method, in order to achieve biaxial stretching at a high magnification because of the solution casting method by the present invention. The film formation is particularly effective. The determination of the total degree of substitution of the thiol group can be carried out in accordance with ASTM-D817-96. The biaxial stretching preferably extends in both the transport direction (MD direction) and the lateral direction (TD direction) of the film.

The weight average molecular weight of the cellulose ester is preferably 5.0×10 ⁴ to 5.0×10 ^{5 , more} preferably 1.0×10 ⁵ to 3.0×10 ⁵ , and 1.5×10 ^{5 in} order to obtain a film having a certain mechanical strength or more. ~2.5×10 ^{5 is} better. The molecular weight distribution (weight average molecular weight Mw / number average molecular weight Mn) of the cellulose ester is preferably from 1.0 to 4.5.

The weight average molecular weight and molecular weight distribution of the cellulose ester can be determined by gel permeation chromatography (GPC). The measurement conditions are as follows.

Solvent: dichloromethane

Pipe column: Three tubes of Shodex K806, K805, and K803G (manufactured by Showa Denko) are used.

Column temperature: 25 ° C

Sample concentration: 0.1% by mass

Detector: RI Model 504 (manufactured by GL Scientific)

Pump: L6000 (Hitachi Manufacturing Co., Ltd.)

Flow rate: 1.0ml/min

Calibration curve: A calibration curve of 13 samples by standard polystyrene STK standard polystyrene (manufactured by Tosoh Corporation) Mw = 1.0 × 10 ⁶ to 5.0 × 10 ² was used. It is preferred that the 13 samples are selected at almost equal intervals.

The cellulose ester is generally synthesized by thiolation of a raw material cellulose corresponding to a mercapto group of a fatty acid (preferably acetic acid) or an anhydride thereof. The cellulose ester can be synthesized by a method described in, for example, JP-A-10-45804.

The raw material cellulose may be wood pulp or cotton linter. The wood pulp can be a conifer or a broadleaf tree. The cellulose ester obtained from the raw material cellulose may be suitably used in combination or used alone.

For example, cellulose esters from cotton linters: cellulose esters from wood pulp (coniferous trees): ratios of cellulose esters from wood pulp (broadleaf trees) are 100:0:0, 90:10:0, 85:15: 0, 50:50:0, 20:80:0, 10:90:0, 0:100:0, 0:0:100, 80:10:10, 85:0:15, 40:30:30 .

Thus, all of the thiol groups are cellulose esters of cellulose acetate (cellulose acetate), and the softness is lower than that of a cellulose ester (cellulose mixed acid ester) such as a fluorenyl group. Therefore, the film of cellulose acetate is generally low in elongation, so that it is difficult to perform biaxial stretching at a high magnification.

The inventors of the present invention have found that the cellulose acetate ester is improved in the elongation of the cellulose acetate by adding "additive having a ring structure" to cellulose acetate. Although the reason is not completely clear, it is presumed that the ring structure of the "additive having a ring structure" is bulky and enters between the molecular chains of cellulose acetate, thereby expanding the chain between the cellulose acetate molecules. Gap.

Further, it has been found that a film obtained by biaxially stretching a film of such a cellulose acetate at a high magnification and a film of a cellulose mixed acid ester such as cellulose acetate propionate are subjected to biaxial rotation at a high magnification. The film obtained by the stretching is different, the white turbidity is small, and the elongation at break in the two extending directions in the film surface is low, and the tensile modulus is high. That is, since the obtained film has less white turbidity, the brightness of the liquid crystal display device can be improved. Moreover, since the obtained film has a low elongation at break in both extending directions and a high tensile modulus, the heat wrinkles of the polarizing plate under high temperature and high humidity or the winding shape when stored in a roll body can be suppressed. Deterioration.

(additive with ring structure)

The additive having a ring structure contains a non-aromatic ring structure or an aromatic ring structure as a ring structure, and is preferably an aromatic ring structure.

The non-aromatic ring structure is preferably a substituted or unsubstituted aliphatic hydrocarbon ring or aliphatic heterocyclic ring having 5 to 22 carbon atoms. Examples of the non-aromatic ring structure include a cyclopentyl ring, a cyclohexyl ring, a norbornyl ring, a cycloheptyl ring, an isodecyl ring, an adamantyl ring, a cyclodecyl ring, a dicyclopentyl ring, an acid anhydride. Ring (for example, -CH-C(=O)OC(=O)-CH-).

The aromatic ring structure is preferably a substituted or unsubstituted aromatic hydrocarbon ring or an aromatic heterocyclic ring having 6 to 23 carbon atoms, more preferably a substituted or unsubstituted aromatic hydrocarbon ring. Examples of the aromatic ring structure include a benzene ring, a naphthalene ring, an anthracene ring, a phenanthrene ring, and the like.

Can have an aliphatic hydrocarbon ring, an aliphatic heterocyclic ring, and an aromatic Examples of the substituent of the hydrocarbon ring or the aromatic heterocyclic ring include an alkyl group having 1 to 3 carbon atoms, an alkoxy group, a cyano group, a hydroxyl group and the like.

The additive having a ring structure is a polyester compound or a styrene compound having a ring structure of a non-aromatic ring structure or an aromatic ring structure, or a caramel structure or a furanose structure having a ring structure in a repeating unit. The structure or furanose structure is preferably a sugar ester compound having a substituent comprising a non-aromatic ring structure or an aromatic ring structure.

Polyester compound

The polyester compound comprises a repeating unit derived from a condensate of a dicarboxylic acid and a diol. The repeating unit preferably comprises a non-aromatic ring structure or an aromatic ring structure. That is, it is preferable that at least one of the dicarboxylic acid and the diol constituting the polyester compound contains a non-aromatic ring structure or an aromatic ring structure, and the dicarboxylic acid contains a non-aromatic ring structure or an aromatic ring structure.

The dicarboxylic acid may be an aliphatic dicarboxylic acid, an alicyclic dicarboxylic acid or an aromatic dicarboxylic acid. The carbon number of the aliphatic dicarboxylic acid is preferably from 4 to 20, more preferably from 4 to 12. Examples of the aliphatic dicarboxylic acid include malonic acid, succinic acid, glutaric acid, adipic acid, pimelic acid, suberic acid, azelaic acid, sebacic acid, undecanedicarboxylic acid, and twelve Alkanedicarboxylic acid and the like.

The carbon number of the aromatic dicarboxylic acid is preferably from 8 to 20, more preferably from 8 to 12. Examples of the aromatic dicarboxylic acid include 1,2-benzenedicarboxylic acid (phthalic acid), 1,3-benzenedicarboxylic acid (isophthalic acid), and 1,4-benzenedicarboxylic acid (p-benzene). Dicarboxylic acid), 1,5-naphthalene dicarboxylic acid, 1,4-dimethylaniline dicarboxylic acid, and the like.

The alicyclic dicarboxylic acid preferably has a carbon number of 6 to 20, more preferably 6 ~12. Examples of the alicyclic dicarboxylic acid include 1,3-cyclobutanedicarboxylic acid, 1,3-cyclopentanedicarboxylic acid, 1,4-cyclohexanedicarboxylic acid, and 1,4-cyclohexane. Alkane diacetic acid and the like.

The dicarboxylic acid constituting the polyester compound may be one type or two or more types. The dicarboxylic acid constituting the polyester compound is preferably an aromatic dicarboxylic acid, and more preferably both an aromatic dicarboxylic acid and an aliphatic dicarboxylic acid are contained. The aromatic dicarboxylic acid is particularly preferred as 1,4-benzenedicarboxylic acid (terephthalic acid).

The diol may be an aliphatic diol, an alkyl ether diol, an alicyclic diol or an aromatic diol. The carbon number of the aliphatic diol is preferably from 2 to 20, more preferably from 2 to 12. Examples of the aliphatic diol include ethylene glycol, 1,2-propylene glycol, 1,3-propanediol, 1,2-butanediol, 1,3-butanediol, 1,2-propanediol (Propanediol), 2-methyl-1,3-propanediol (Propanediol), 1,4-butanediol, 1,5-pentanediol, 2,2-dimethyl-1,3-propanediol (Propanediol) (neopentylene glycol) ), 2,2-diethyl-1,3-propanediol (3,3-dihydroxymethylpentane), 2-n-butyl-2-ethyl-1,3-propanediol (3,3- Dimethylol heptane), 3-methyl-1,5-pentanediol, 1,6-hexanediol, 2,2,4-trimethyl-1,3-pentanediol, 2-B Base-1,3-hexanediol, 2-methyl-1,8-octanediol, 1,9-nonanediol, 1,10-nonanediol, and 1,12-octadecanediol . The alkyl ether diol preferably has a carbon number of 4 to 20, more preferably 4 to 12. Examples of the alkyl ether glycol include polytetramethylene ether glycol, polyvinyl ether glycol, and polypropylene ether glycol.

The alicyclic diol preferably has a carbon number of 4 to 20, more preferably 4 to 12. Examples of the alicyclic diol include 1,4-cyclohexanediol, 1,4-cyclohexanedimethanol, and the like.

The carbon number of the aromatic diol is preferably from 6 to 20, more preferably from 6 to 12. Examples of the aromatic diol include 1,2-dihydroxybenzene (catechol), 1,3-dihydroxybenzene (resorcinol), 1,4-dihydroxybenzene (hydroquinone), and the like. .

The diol constituting the polyester compound may be one type or two types. The diol constituting the polyester compound preferably contains an aliphatic diol.

Among these, a dicarboxylic acid containing an aromatic dicarboxylic acid and an aliphatic dicarboxylic acid, and a polyester compound containing a repeating unit derived from a condensate with an aliphatic diol, extensibility and transparency from a film containing the same Good sex is better.

The molecular end of the polyester compound may be sealed with a monocarboxylic acid or a monool if necessary.

The monocarboxylic acid may be an aliphatic monocarboxylic acid, an alicyclic monocarboxylic acid or an aromatic monocarboxylic acid. The carbon number of the aliphatic monocarboxylic acid is preferably from 2 to 30, more preferably from 2 to 4. Examples of the aliphatic carboxylic acid include acetic acid, propionic acid, butyric acid, caprylic acid, caproic acid, capric acid, dodecanoic acid, stearic acid, oleic acid and the like. Examples of the alicyclic monocarboxylic acid include a cyclohexylmonocarboxylic acid and the like. Examples of the aromatic monocarboxylic acid include benzoic acid, tert-butylbenzoic acid, o-toluic acid, m-toluic acid, p-toluic acid, dimethylbenzoic acid, ethylbenzoic acid, n-propylbenzoic acid, and amine. Benzoic acid, ethoxylated benzoic acid, phenylacetic acid, 3-phenylpropionic acid, and the like.

The monool can be an aliphatic monol, an alicyclic monol or an aromatic monool. The aliphatic monool has a carbon number of 1 to 30, preferably 1 to 3. Examples of the aliphatic monool include methanol, ethanol, propanol, isopropanol, butanol, isobutanol, pentanol, isoamyl alcohol, hexanol, isohexanol, octanol, isooctanol, 2-ethyl Hexyl alcohol, mercapto alcohol, isodecyl alcohol, tert-mercapto alcohol, sterol, Decylene, dodecyl hexanol, dodecanoic alcohol, allyl alcohol, oleyl alcohol, and the like. Examples of the alicyclic monool include cyclohexyl alcohol and the like. Examples of the aromatic monool include benzyl alcohol, 3-phenylpropanol and the like.

Specific examples of the polyester compound having a ring structure include the following. Table 1 below describes TPA: terephthalic acid, PA: phthalic acid, SA: succinic acid, AA: adipic acid, and SEA: sebacic acid.

Styrene compound

The styrene-based compound may be a single polymer of a styrene-based monomer, and may be a copolymer of a styrene-based monomer and a copolymerized monomer other than the styrene-based monomer. The content ratio of the constituent unit derived from the styrene-based monomer in the styrene-based compound is preferably from 30 to 100 mol%, more preferably from 50 to 100 mol%, because the molecular structure has a certain bulk or more. %.

The styrene monomer is preferably a compound represented by the following formula (1).

R ¹⁰¹ to R ¹⁰³ in the formula (1) each independently represent a hydrogen atom or an alkyl group or an aryl group having 1 to 30 carbon atoms. R ¹⁰⁴ represents a hydrogen atom, an alkyl group having 1 to 30 carbon atoms, a cycloalkyl group, an aryl group, an alkoxy group having 1 to 30 carbon atoms, an aryloxy group, an alkoxycarbonyl group having 2 to 30 carbon atoms, or an aryloxy group. A carbonyl group, an alkylcarbonyloxy group having 2 to 30 carbon atoms, an arylcarbonyloxy group, a hydroxyl group, a carboxyl group, a cyano group, an amine group, a decylamino group, and a nitro group. These groups may further have a substituent (for example, a hydroxyl group, a halogen atom, an alkyl group, etc.), respectively. R ¹⁰⁴ may be the same or different, and may be bonded to each other to form a ring.

Examples of the styrene monomer include styrene; alkyl-substituted styrenes such as α-methylstyrene, β -methylstyrene, and p-methylstyrene; 4-chlorostyrene, 4- Halogen-substituted styrenes such as bromostyrene; hydroxyl groups such as p-hydroxystyrene, α -methyl-p-hydroxystyrene, 2-methyl-4-hydroxystyrene, and 3,4-dihydroxystyrene Styrene; vinyl benzyl alcohol; alkoxy-substituted styrenes such as p-methoxystyrene, p-tert-butoxystyrene, m-tert-butoxystyrene; Vinyl benzoic acid, vinyl benzoic acid such as 4-vinyl benzoic acid; 4-vinylbenzyl acetate; 4-ethyl methoxy styrene; 2-butyl decyl styrene, 4-methyl Amidoxime styrene, p-melamine styrene, etc.; 3-aminostyrene, 4-aminostyrene, 2-isopropenylaniline, vinylbenzyldimethylamine Aminostyrenes; nitrostyrenes such as 3-nitrostyrene and 4-nitrostyrene; cyanostyrenes such as 3-cyanostyrene and 4-cyanostyrene; Vinyl phenyl acetonitrile; aryl benzene such as phenyl styrene Alkenes, indene and so on. The styrene monomer may be one type or a combination of two or more types.

The copolymerized single system combined with the styrene monomer comprises a (meth) acrylate compound represented by the following formula (2), maleic anhydride, citraconic anhydride, and cis-1-cyclohexene-1. 2-dicarboxylic anhydride, 3-methyl-cis-1-cyclohexene-1,2-dicarboxylic anhydride, 4-methyl-cis-1-cyclohexene-1,2-dicarboxylic anhydride, etc. a radically polymerizable monovalent body containing a nitrile group such as an acid anhydride, acrylonitrile or methacrylonitrile; acrylamide, methacrylamide, trifluoromethanesulfonylamino group a radically polymerizable monovalent body containing a guanamine bond such as an ethyl (meth) acrylate; a fatty acid vinyl group such as a vinyl acetate; a radical polymerization containing chlorine such as a vinyl chloride or a vinyl chloride; The conjugated diene such as 1,3-butadiene, isoprene or 1,4-dimethylbutadiene is preferably represented by the following formula (2) ( Methyl) acrylate compound or maleic anhydride.

R ¹⁰⁵ to R ¹⁰⁷ in the formula (2) each independently represent a hydrogen atom or an alkyl group or an aryl group having 1 to 30 carbon atoms. R ¹⁰⁸ represents a hydrogen atom, an alkyl group having 1 to 30 carbon atoms, a cycloalkyl group, or an aryl group. These groups may further have a substituent (for example, a hydroxyl group, a halogen atom, an alkyl group, etc.), respectively.

Examples of the (meth) acrylate-based compound include methyl (meth) acrylate, ethyl (meth) acrylate, propyl (meth) acrylate (i-, n-), and (meth) acrylate. Ester (n-, i-, s-, tert-), amyl (meth)acrylate (n-, i-, s-), hexyl (meth)acrylate (n-, i-), (A) (meth)heptyl acrylate (n-, i-), octyl (meth) acrylate (n-, i-), decyl (meth) acrylate (n-, i-), (meth) acrylate nutmeg Ester (n-, i-), (meth) propylene Acid (2-ethylhexyl), (meth)acrylic acid (ε-caprolactone), (meth)acrylic acid (2-hydroxyethyl), acrylic acid (2-hydroxypropyl), (meth)acrylic acid ( 3-hydroxypropyl), (4-hydroxybutyl) (meth)acrylate, (2-hydroxybutyl) (2-hydroxyethyl), (2-methoxyethyl)acrylate, (meth)acrylic acid ( Phenyl 2-ethoxyethyl)acrylate, phenyl (meth) methacrylate, (meth)acrylic acid (2 or 4-chlorophenyl), (meth)acrylic acid (2 or 3 or 4-ethyl) Oxycarbonylphenyl), (meth)acrylic acid (o or m or p-tolyl), benzyl (meth)acrylate, phenethyl (meth)acrylate, (meth)acrylic acid (2-naphthyl) ), cyclohexyl (meth)acrylate, (meth)acrylic acid (4-methylcyclohexyl), (meth)acrylic acid (4-ethylcyclohexyl), and the like.

Specific examples of the styrene-based compound include a styrene/maleic anhydride copolymer, a styrene/acrylate copolymer, a styrene/hydroxystyrene polymer, a styrene/acetoxystyrene polymer, and the like. Among them, a styrene/maleic anhydride copolymer is preferred.

Sugar ester compound

A sugar ester compound is a compound obtained by esterifying a hydroxyl group contained in a sugar with a monocarboxylic acid.

The sugar constituting the sugar ester compound is more preferably a compound having at least one of a furanose structure and a carnosylose structure having a structure in which one or more and 12 or less bonds are bonded.

Examples of the sugar constituting the sugar ester compound include monosaccharides such as glucose, galactose, mannose, fructose, xylose, and arabinose; disaccharides such as lactose, sucrose, maltitol, cellobiose, and maltose; Trisaccharide such as trisaccharide or raffinose. Among them, sugar having both a sucrose structure and a furanose structure is preferred, and sucrose is preferred.

The monocarboxylic acid constituting the sugar ester compound may be an aliphatic monocarboxylic acid, an alicyclic monocarboxylic acid or an aromatic monocarboxylic acid. In order to obtain a bulky sugar ester compound, the monocarboxylic acid constituting the sugar ester compound preferably contains an alicyclic monocarboxylic acid or an aromatic monocarboxylic acid, and more preferably contains an aromatic monocarboxylic acid. The monocarboxylic acid may be one type or two or more types. For example, an aliphatic monocarboxylic acid and an aromatic monocarboxylic acid can be combined.

Examples of the aliphatic monocarboxylic acid include acetic acid, propionic acid and the like. Examples of the alicyclic monocarboxylic acid include cyclopentanecarboxylic acid, cyclohexanecarboxylic acid and the like. Examples of the aromatic monocarboxylic acid include benzoic acid, phenylacetic acid, and the like.

The sugar ester compound is preferably a compound represented by the following formula (3).

R ₁ to R _{8 of the} formula (3) represent a monovalent group derived from an aliphatic monocarboxylic acid, a monovalent group derived from an alicyclic monocarboxylic acid, or derived from an aromatic monocarboxylic acid. The monovalent group; at least one of R ₁ to R ₈ is a monovalent group derived from an alicyclic monocarboxylic acid, or a monovalent group derived from an aromatic monocarboxylic acid. R ₁ to R ₈ may be the same or different.

Examples of the monovalent group derived from the aliphatic monocarboxylic acid include a monovalent group derived from an aliphatic monocarboxylic acid having 2 or more carbon atoms such as methylcarbonyl (ethinyl). An example of a monovalent group derived from an alicyclic monocarboxylic acid, which comprises a monovalent group derived from an alicyclic monocarboxylic acid having 5 or more carbon atoms of a cyclopentylcarboxylic acid or a cyclohexylcarboxylic acid. base. Examples of the monovalent group derived from the aromatic monocarboxylic acid include an aromatic monocarboxylic acid having 7 or more carbon atoms such as a phenylcarbonyl group (benzimidyl group) or a phenylmethylcarbonyl group. The basis of the price. The non-aromatic ring derived from the monovalent group derived from the alicyclic monocarboxylic acid or the aromatic ring derived from the monovalent group derived from the aromatic monocarboxylic acid may further have an alkyl group or an alkoxy group or the like. base.

Among them, R ₁ to R ₈ are preferably a monovalent group derived from an aromatic monocarboxylic acid.

Specific examples of the compound represented by the formula (3) include the following. R in the following table represents R ₁ to R ₈ in the formula (3).

The average degree of substitution of the sugar ester compound is preferably 3.0 to 8.0, and particularly preferably 5.0 to 8.0. When a substituent bonded to a carbon atom constituting a sucrose structure or a furanose structure includes a non-aromatic ring structure or an aromatic ring structure, when the average degree of substitution is in the above range, the bulk of the sugar ester compound is easily fixed. the above.

A sugar ester compound having such a ring structure may be used in combination with a sugar ester having no ring structure, if necessary. Examples of the sugar ester compound having no ring structure include the following. R in the following table represents R ₁ to R _{8 of the} following formula (A).

Among these, because the molecular structure has sufficient bulk, the repeating unit is a polyester compound having an aromatic ring structure and a styrene compound. The sugar ester compound having an aromatic ring structure is preferable, and the molecular structure can be said to have a chain structure, and the repeating unit has a structure having an aromatic ring structure because it is easy to increase the elongation of the film (it is easy to obtain a plasticizing effect). The ester compound and the styrene compound are more preferable.

The additive having a ring configuration, as described above, is present between the cellulose ester molecules to expand the spacing between the molecular chains of the cellulose ester. It is considered that the elongation of the film can be improved by it. Therefore, it is preferable that the additive having a ring structure has sufficient bulkiness in its molecular structure, and it is preferable to have a large amount of ring-containing structure.

The bulkiness of the additive having a ring structure can be evaluated by the "bulkness index" defined by the following formula.

Bulking index = sum of molecular weights of the ring structure portion / molecular weight of the entire additive having a ring structure

The "ring structure portion" in the above formula means a non-aromatic ring structure or an aromatic ring structure itself. When a non-aromatic ring structure or an aromatic ring structure has a substituent, the substituent is also considered to be part of the ring structure. For example, the "ring structure portion" of the exemplified compound 6 of the polyester of Table 1 above is a phenyl group derived from terephthalic acid (-C ₆ H ₄ -) and a phenyl group derived from benzoic acid (-C ₆ H ₅ ). . The "ring structure portion" of the styrene/maleic anhydride copolymer is a phenyl group (-C ₆ H ₅ ) constituting styrene and -CHC(=O)OC(=O)CH- derived from maleic anhydride. The "ring structure portion" of the styrene/hydroxystyrene copolymer is a phenyl group (-C ₆ H ₅ ) constituting styrene and a hydroxyphenyl group (-C ₆ H ₄ OH) constituting hydroxystyrene. The "ring structure portion" of the sugar ester compound represented by the above formula (FA-1) is a benzene which is bonded to a carbon atom constituting a sucrose structure or a furanose structure, and a substituent other than the bond glycoside. Base (-C ₆ H ₅ ).

The bulkiness index of the additive having a ring structure is preferably 0.2 or more, more preferably 0.6 or more. The upper limit of the "looseness index" may be, for example, 0.9.

The weight average molecular weight of the additive having a ring structure is preferably 10,000 or less, and more preferably 5,000 or less, in order to ensure compatibility with a cellulose ester or the like. The weight average molecular weight of the additive having a ring structure is preferably 300 or more, and more preferably 400 or more, in order to suppress bleeding or the like.

When the repeating unit is a polyester compound or a styrene compound having an aromatic ring structure, the weight average molecular weight of the compounds is easy to increase the elongation of the film, and the tensile modulus of the film after stretching is also It is easy to increase, etc., so it is preferably 600 or more, more preferably 1,000 or more, and even more preferably 2,000 or more.

The content of the additive having a ring structure is preferably 5 to 30% by mass based on the cellulose ester, and more preferably 5 to 20% by mass. When the content of the additive having a ring structure is less than 5% by mass, the interval between the cellulose ester molecular chains may not be sufficiently enlarged. When the content of the additive having a ring structure exceeds 30% by mass, not only is it easy to bleed out from the film, but also the elongation at break is improved.

Other additives

The optical film of the present invention may further contain a plasticizer, purple if necessary Various additives such as external absorbents, matting agents (fine particles).

Plasticizer

In the case of the plasticizer, a polyester compound, a polyol ester compound or the like which does not have a ring structure among the above polyester compounds is contained. The polyol ester-based compound includes, for example, a compound described in paragraphs 0218 to 0170 of JP-A-2010-32655.

The content of the plasticizer is preferably from 1 to 40% by mass, more preferably from 5 to 20% by mass, based on the cellulose ester.

UV absorber

The optical film of the present invention may further contain an ultraviolet absorber. Examples of the ultraviolet absorber include a benzotriazole-based compound, a 2-hydroxybenzophenone-based compound, and a phenyl salicylate-based compound.

Among them, the ultraviolet absorber having a molecular weight of 400 or more is difficult to sublimate or is difficult to volatilize at a high boiling point, and is difficult to fly when the film is dried at a high temperature, and is preferable from the viewpoint of improving the weather resistance with a relatively small amount of addition effect. Examples of the ultraviolet absorber having a molecular weight of 400 or more include 2-[2-hydroxy-3,5-bis(α,α-dimethylbenzyl)phenyl]-2-benzotriazole, 2,2. - a benzotriazole system such as methyl bis[4-(1,1,3,3-tetrabutyl)-6-(2H-benzotriazol-2-yl)phenol]; Blocking of 2,6,6-tetramethyl-4-piperidinyl) sebacate, bis(1,2,2,6,6-pentamethyl-4-piperidyl)sebacate Amine, further 2-(3,5-di-t-butyl-4-hydroxybenzyl)-2-n-butylmalonic acid bis(1,2,2,6,6-pentamethyl -4-piperidinyl), 1-[2-[3-(3,5-di- T-butyl-4-hydroxyphenyl)propanoxy]ethyl]-4-[3-(3,5-di-t-butyl-4-hydroxyphenyl)propanoxy]-2 And a mixture of a hindered phenol and a hindered amine in the molecule of 2,6,6-tetramethylpiperidine or the like, and these may be used alone or in combination of two or more. Among them, 2-[2-hydroxy-3,5-bis(α,α-dimethylbenzyl)phenyl]-2-benzotriazole or 2,2-extended methyl bis[4-(1 , 1,3,3-tetrabutyl)-6-(2H-benzotriazol-2-yl)phenol] is particularly preferred.

The ultraviolet absorber may be a commercially available product, and for example, TINUVIN 109, TINUVIN 171, TINUVIN 234, TINUVIN 326, TINUVIN 327, TINUVIN 328, TINUVIN 928, etc., or 2, 2'-, manufactured by BASF Japan, may be used. Methyl bis[6-(2H-benzotriazol-2-yl)-4-(1,1,3,3-tetramethylbutyl)phenol] (molecular weight 659; as an example of a commercial product, LA31, a company limited by ADEKA.

The content of the ultraviolet ray inhibitor is preferably from 1 ppm to 1000 ppm by mass in the optical film, more preferably from 10 to 1,000 ppm.

Matting agent

The optical film of the present invention may further contain a matting agent in order to impart slidability. The matting agent may be an inorganic compound or an organic compound as long as it does not impair the transparency of the obtained film and has heat resistance during melting. The matting agent may be used alone or in combination of two or more.

Among them, it is particularly preferable to use cerium oxide which is close to the refractive index of the cellulose ester and which is excellent in transparency (haze value) of the film. As a specific example of cerium oxide, it is preferable to use Aerosil 200V, Aerosil R972V, Aerosil R972, R974, R812, 200, 300, R202, OX50, TT600, NAX50 (above Japan Aerosil Co., Ltd.), SEAHOSTAR KEP-10, SEAHOSTAR KEP-30, SEAHOSTAR KEP-50 (above is Japan Catalyst Limited) Commercial products of the company name, Sylophobic 100 (manufactured by Fuji Silicia), Nipseal E220A (manufactured by Nippon Seika Co., Ltd.), ADMAFINE SO (manufactured by Admatechs Co., Ltd.), and the like.

The shape of the particles is indefinite, needle-like, flat, spherical, and the like, and is not particularly limited. When spherical particles are used, the transparency of the obtained film is preferably good.

When the size of the particles is close to the wavelength of visible light, light is scattered. Since the transparency is deteriorated, it is preferably smaller than the wavelength of visible light, and more preferably 1/2 or less of the wavelength of visible light. When the size of the particles is too small, since the slidability cannot be improved, it is preferably in the range of from 80 nm to 180 nm. The size of the particles means the size of the aggregate when the particles are agglomerates of primary particles. Moreover, it means that the particle corresponds to the diameter of the circle of the projected area when the particle is not spherical.

The content of the matting agent may be from about 0.05 to 1.0% by mass, preferably from 0.1 to 0.8% by mass, based on the cellulose ester.

The optical film of the present invention may be a single layer film or a laminated film. In the case of laminating a film, it is preferred that the entire layer constituting the optical film contains the cellulose ester described above and an additive having a ring structure.

The thickness of the optical film of the present invention is preferably 15 to 35 μm, more preferably 15 to 30 μm. When the thickness is less than 15 μm, the strength of the film may not be sufficient. When the thickness exceeds 35 μm, for example, it is a portable liquid crystal display. The optical film used in the device is sometimes too thick.

As described later, the optical film of the present invention is obtained by biaxially stretching at a high magnification by using a film having a thiol group of cellulose ester as a main component. Therefore, the optical film of the present invention has less white turbidity (low haze value), and has high tensile modulus in both extending directions and a certain breaking elongation in both extending directions.

[Tensile modulus]

The direction of the slow axis of the optical film of the present invention and the direction perpendicular to the direction of the slow axis are perpendicular to the tensile modulus at 23 ° C and 55 RH, preferably 3.0 to 8.5 GPa, more preferably 5.0 to 8.0 GPa.

The retardation axis in the plane of the optical film is the axis in which the refractive index in the plane of the optical film becomes the largest. The slow phase axis in the plane of the optical film can be specified by KOBRA21ADH as will be described later. The retardation axis in the plane of the optical film may be, for example, the MD direction of the optical film (in the longitudinal direction of the optical film of the roll body) or the TD direction (the transverse direction of the optical film of the roll body).

In particular, when a polarizing plate is obtained by laminating a polarizer and an optical film in a roll-to-roll manner, in order to increase the balance of the tensile modulus in the TD/MD direction of the polarizing plate, it is compared with the absorption axis direction of at least the photon of the optical film ( The MD direction) is preferably a tensile modulus higher than the vertical direction (TD direction). The tensile modulus of elasticity in the direction perpendicular to the absorption axis direction (MD direction) of the optical film (TD direction) is preferably 5.0 to 8.0 GPa.

Stretching of the optical film in the direction of the slow axis (for example, MD direction) The modulus of elasticity can be determined by the following method. First, the optical film was cut into a size of 100 mm (MD direction) × 10 mm (TD direction) to prepare a sample film. The sample film was subjected to Tensilon RTC-1225A manufactured by Orientec Co., Ltd. according to JIS K7127, and the distance between the chucks was set to 50 mm, and the film was stretched in the direction of the slow axis (for example, MD direction) to measure the direction of the slow axis (for example, the MD direction). Tensile modulus. The measurement can be carried out at 23 ° C, 55% RH.

The tensile modulus of elasticity in a direction perpendicular to the retardation axis of the optical film (for example, the TD direction) may be changed from the direction in which the direction of the stretched sample film is changed to the direction perpendicular to the slow axis (for example, the TD direction). Determined in the same manner.

[Elongation at break]

The retardation axis direction of the optical film of the present invention and the direction perpendicular thereto at 23 ° C and 55% RH are preferably from 1 to 10%, more preferably from 1 to 5%.

The elongation at break of the retardation axis direction (for example, the MD direction) of the optical film can be measured by the following method. First, the optical film was cut into a size of 100 mm (MD direction) × 10 mm (TD direction) as a sample film. Next, the sample film was Tensilon RTC-1225A manufactured by Orientec Co., Ltd., and the distance between the chucks was set to 50 mm, and the film was stretched in the direction of the slow axis (for example, MD direction) to determine the elongation at break from the breaking point of the film. The measurement was carried out under the conditions of a tensile speed of 50 mm/min at 23 ° C and a 55% RH atmosphere.

a direction perpendicular to the retardation axis of the optical film (for example, TD square) The elongation at break of the film can be measured in the same manner as described above except that the direction in which the sample film is stretched is changed to a direction perpendicular to the slow axis (for example, the TD direction).

The elongation at break (or tensile modulus) of the optical film can be adjusted, for example, by the total degree of substitution of the thiol group of the cellulose ester (the degree of substitution of the cellulose acetate to the thiol group), the type of the additive, the elongation conditions, and the like. . In order to reduce the elongation at break (or increase the tensile modulus) of the optical film, for example, a cellulose ester having a high total substitution degree of sulfhydryl groups or a polyester compound or a styrene compound having a certain molecular weight or more may be selected, or the elongation may be increased. The magnification can be.

[fog value]

As described above, the optical film of the present invention has less white turbidity and can reduce the haze value. The optical film of the present invention preferably has a haze value of 1.0% or less, more preferably 0.5% or less. When the optical film of the present invention is used as a scattering film, the haze value may exceed the above range. The haze value is measured in accordance with JIS K-7136 using a haze meter (turbidity meter) (type: NDH 2000, manufactured by Nippon Denshoku Co., Ltd.).

[delay]

The optical film of the present invention can preferably have a retardation R ₀ measured in the in-plane direction at a wavelength of 590 nm, 23 ° C, and 55% RH to satisfy 0 ≦ R ₀ ≦ 20 nm, preferably 0 nm ≦ R ₀ ≦ 10 nm. . The retardation Rth in the thickness direction of the optical film which can be measured under the conditions of measuring wavelengths of 590 nm, 23 ° C, and 55% RH is preferably 0 nm ≦ Rth ≦ 80 nm, more preferably 0 nm ≦ Rth ≦ 50 nm. The optical film having such a retardation value is preferably used as a protective film (F1/F4) of a liquid crystal display device as will be described later.

R ₀ and Rth can be adjusted by the total degree of substitution or extension conditions of the thiol group of the cellulose ester. In order to reduce R ₀ , for example, the total degree of substitution of the thiol group of the cellulose ester may be increased, or the difference of the stretching ratio in the TD/MD direction may be reduced.

The delays R ₀ and Rth are respectively defined by the following equations.

Formula (I): R ₀ = (nx - ny) × d (nm)

Formula (II): Rth={(nx+ny)/2-nz}×d(nm)

(In the formulae (I) and (II), nx represents the refractive index in the in-plane direction x of the optical film in which the refractive index becomes maximum; ny represents the late in the in-plane direction of the optical film. The refractive index of the direction of the phase axis x perpendicular to the direction y; nz represents the refractive index in the thickness direction z of the optical film; d (nm) represents the thickness of the optical film)

The delays R ₀ and Rth can be obtained, for example, by the following method.

1) The optical film was conditioned at 23 ° C, 55% RH. The average refractive index of the optical compensation film after the humidity adjustment is measured by an Abbe refractometer or the like.

2) After the optical film to the humidity, incident parallel to the R ₀ of Time measured normal to the surface of the film light having a wavelength of 590nm to KOBRA21DH, Oji (shares) assay.

3) From KOBRA21ADH, the slow phase axis in the plane of the optical film is used as the tilt axis (rotary axis), and the normal line of the surface of the optical film is measured from θ The angle (incident angle (θ)) is a retardation value R(θ) when incident light having a wavelength of 590 nm is incident. The retardation value R(θ) is measured in the range of θ from 0° to 50°, and can be performed every 10°. The retardation axis in the plane of the optical film can be confirmed by KOBRA21ADH.

4) From the measured R ₀ and R (θ), and the average refractive index and film thickness described above, nx, ny, and nz were calculated from KOBRA21ADH, and Rth at a measurement wavelength of 590 nm was calculated. The measurement of the retardation can be carried out at 23 ° C, 55% RH.

The angle θ1 (alignment angle) between the in-plane slow axis of the optical film and the width direction of the film is preferably -1 to +1, more preferably -0.5 to +0.5. The measurement of the alignment angle θ1 of the optical film can be measured using an automatic birefringence analyzer KOBRA-WR (Prince Measurement Machine).

The optical film of the present invention has a total light transmittance of preferably 90% or more, more preferably 93% or more.

The functional layer of the hard coat layer, the antistatic layer, the undercoat layer, the antireflection layer, the slippery layer, the adhesive layer, the antiglare layer, and the barrier layer may be further laminated on the optical film of the present invention.

[hard coating]

The hard coat layer contains a cured product of an active wire hardening compound. As the active wire curable compound, a component containing a monomer having an ethylenically unsaturated double bond is preferably used. The active curable compound is an ultraviolet curable compound or an electron beam curable compound, but the compound hardened by ultraviolet irradiation is excellent in mechanical film strength (scratch resistance, pencil hardness). This is better at this point.

Examples of the ultraviolet curable compound include ultraviolet curable urethane acrylate resin, ultraviolet curable polyester acrylate resin, ultraviolet curable epoxy acrylate resin, and ultraviolet curable polyol acrylate. A resin, or an ultraviolet curable epoxy resin or the like is preferable. Among them, an ultraviolet curable acrylate resin is preferred.

The hard coat layer is obtained by applying a coating liquid for a hard coat layer containing a reactive wire curable compound and a photopolymerization initiator to an optical film, followed by curing by irradiation with an active wire.

Specific examples of the photopolymerization initiator include acetophenone, benzophenone, hydroxybenzophenone, Michler's ketone, α -amyl oxime ester, thioxanthone, and the like. Derivatives, but are not particularly limited thereto. The photopolymerization starting dose in the coating liquid for a hard coat layer is preferably in a mass ratio of a photopolymerization initiator: active line curable compound = 20:100 to 0.01:100.

The coating liquid for a hard coat layer may further contain inorganic fine particles or organic fine particles as necessary. Examples of the inorganic fine particles include cerium oxide, titanium oxide, aluminum oxide, tin oxide, indium oxide, ITO, zinc oxide, zirconium oxide, magnesium oxide, calcium carbonate, talc, clay, calcined kaolin, and calcined calcium citrate. As the hydrated calcium citrate, aluminum silicate, magnesium citrate and calcium phosphate, cerium oxide, titanium oxide, aluminum oxide, zirconium oxide, magnesium oxide or the like is preferably used.

In the case of organic microparticles, polymethyl methacrylate is included. Acrylate resin powder, acrylic styrene resin powder, polymethyl methacrylate resin powder, fluorene resin powder, and the like.

The average particle diameter of the fine particles is not particularly limited. However, in consideration of the fact that the antiglare layer can be formed, it is preferably in the range of 0.01 to 5 μm, more preferably in the range of 0.01 to 1.0 μm. Further, two or more kinds of fine particles having different particle diameters may be contained. The average particle diameter of the microparticles can be measured, for example, by a laser diffraction type particle size distribution measuring apparatus.

The content of the fine particles is preferably in the range of 10 to 400 parts by mass, more preferably 50 to 200 parts by mass, based on 100 parts by mass of the ultraviolet curable compound.

These hard coat layers are coated with a hard coat layer by a known method such as a gravure coater, a dip coater, a reverse coater, a bar coater, a die coater, or an inkjet method. The cloth composition is heated and dried after coating, and can be formed by UV curing treatment.

The dry film thickness of the hard coat layer is in the range of 0.1 to 30 μm, preferably 1 to 20 μm, and particularly preferably 6 to 15 μm.

As a light source for the UV hardening treatment, it is not limited as long as it is a light source capable of generating ultraviolet rays. For example, a low pressure mercury lamp, a medium pressure mercury lamp, a high pressure mercury lamp, an ultra high pressure mercury lamp, a carbon arc lamp, a metal halide lamp, a xenon lamp, or the like can be used.

Although the irradiation conditions differ depending on various lamps, the irradiation amount of the active rays is usually in the range of 5 to 500 mJ/cm ² , preferably in the range of 5 to 200 mJ/cm ² .

[anti-reflection layer]

The optical film of the present invention can be further laminated with an antireflection layer on the hard coat layer. By this, the optical film of the present invention can be used as an antireflection film having an external light antireflection function.

The antireflection layer is preferably laminated in consideration of a refractive index, a film thickness, a number of layers, a layer order, and the like in such a manner that the reflectance is reduced by optical interference. The antireflection layer is preferably a combination of a low refractive index layer having a lower refractive index than a support (the optical film described above) or a higher refractive index layer and a lower refractive index layer having a higher refractive index than the support. Particularly preferred is an antireflection layer composed of three or more refractive index layers, and three layers having different refractive indices from the support side are used to use a medium refractive index layer (higher refractive index than the support, higher refractive index) It is preferred that the layer of the lower refractive index layer/high refractive index layer/low refractive index layer be laminated. Alternatively, it is preferable to use an antireflection layer which is formed by alternately laminating two or more layers of a high refractive index layer and two or more layers of a low refractive index layer.

The layer constitution of the antireflection film is considered to be as follows, but is not limited thereto.

Optical film / hard coat / low refractive index layer

Optical film / hard coat / medium refractive index layer / low refractive index layer

Optical film / hard coat / medium refractive index layer / high refractive index layer / low refractive index layer

Optical film / hard coat layer / high refractive index layer (conductive layer) / low refractive index layer

Optical film / hard coat / anti-glare layer / low refractive index layer

It is preferable that the low refractive index layer which is necessary for the antireflection film contains cerium oxide-based fine particles. The refractive index of cerium oxide microparticles The holding body (the aforementioned optical film) has a lower refractive index, preferably in the range of 1.30 to 1.45 at 23 ° C and a wavelength of 550 nm. The cerium oxide-based fine particles are preferably particles having at least one type of porous or voids inside the outer shell layer. In particular, although the inside of the outer shell layer is porous or hollow, it is preferable to use hollow ceria-based fine particles.

The film thickness of the low refractive index layer is preferably 5 nm to 0.5 μm, more preferably 10 nm to 0.3 μm, and most preferably 30 nm to 0.2 μm.

The low refractive index layer can be obtained by applying and drying a coating liquid for a low refractive index layer and then curing it. The coating liquid for a low refractive index layer contains the above-mentioned ceria-based fine particles, and may further contain an organic antimony compound represented by the following formula (4) or a hydrolyzate thereof, or a polycondensate thereof.

Formula (4): Si(OR) ₄

An organic phosphonium compound represented by the formula (4): wherein R represents an alkyl group having 1 to 4 carbon atoms. Specifically, tetramethoxy decane, tetraethoxy decane, tetraisopropoxy decane or the like is preferably used.

The coating liquid for a low refractive index layer may further contain a solvent, a decane coupling agent, a curing agent, a surfactant, etc., if necessary.

2. Method for manufacturing optical film

The optical film of the present invention can be produced by a solution casting method or a melt casting method from the viewpoints of suppression of coloring, suppression of defects of foreign matter, suppression of optical defects such as a die line, and the like. Among them, because of the flatness and ribs of the obtained film It is preferable to use a solution casting method because the failure resistance, the accuracy of the film thickness, and the like are good.

The optical film of the present invention produced by the solution casting method is doped by dissolving a cellulose ester, an additive having a ring structure having a molecular weight of 10,000 or less, and other additives as necessary in a solvent. a step of solution, 2) a step of casting the doping solution on the endless metal support, 3) a step of drying the cast doping solution to obtain a film obtained by peeling the metal support, and 4) stretching the film Preferably, the step of 5) is carried out by rolling up the stretched film.

1) Dissolution step

The organic solvent which is useful in the preparation of the doping solution is not limited as long as it can dissolve the cellulose ester or the additive having a ring structure at the same time.

For example, as the chlorine-based organic solvent, dichloromethane is mentioned. Examples of the non-chlorine organic solvent include methyl acetate, ethyl acetate, amyl acetate, acetone, tetrahydrofuran, 1,3-dioxolane (Dioxolan), 1,4-dioxane, cyclohexanone, and formic acid. Ethyl ester, 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, and the like. Among them, methyl chloride, methyl acetate, ethyl acetate, acetone, etc. are preferred.

In the doping, in addition to the above organic solvent, a linear or branched aliphatic group containing 1 to 40% by mass of carbon atoms and 1 to 4 carbon atoms Alcohol is preferred. By causing the alcohol to be contained in the doping solution, the film is gelated, and the peeling by the metal support is facilitated.

Examples of the linear or branched aliphatic alcohol having 1 to 4 carbon atoms include methanol, ethanol, n-propanol, iso-propanol, n-butanol, sec-butanol, and tert-butanol. From the viewpoints of the stability of the internal doping, the boiling point is also relatively low, and the drying property is also good, ethanol is preferred.

In particular, a solvent containing a linear or branched aliphatic alcohol having dichloromethane and a carbon number of 1 to 4 is preferably at least 15 to 45% by mass of the cellulose ester and the additive having a ring structure.

For the dissolution of the cellulose ester or the like, the method is carried out by a method of normal pressure, a method of performing the pressure below the boiling point of the main solvent, or a method of pressurizing at a boiling point or higher of the main solvent, such as Japanese Patent Laid-Open No. Hei 9-95544, Japan. Various methods such as a method of performing a cooling and dissolving method described in Japanese Laid-Open Patent Publication No. Hei 9-95538, and a method of performing high pressure as described in JP-A-11-21379, but In particular, it is preferred to carry out the method of pressurizing at a temperature higher than the boiling point of the main solvent.

The concentration of the cellulose ester or the like in the doping solution may be in the range of 15 to 45% by mass in total.

The filtration system is preferably a filter medium having a collection particle diameter of 0.5 to 5 μm and a filtration time of 10 to 25 sec/100 ml.

In this method, the agglomerates remaining when the particles are dispersed or the agglomerates generated when the main doping is added can be used in the range of 0.5 to 5 μm of the collected particle diameter, and the drainage time is 10 to 25 sec. The filter material in the range of /100 ml only removes aggregates. Main doping because of the concentration of particles The addition liquid is also very thin, and the filtration does not adhere to each other during filtration, so that the filtration pressure rises sharply.

2) Casting step

The doping solution is supplied to the pressurizing mold through a liquid feeding pump (for example, a pressurized quantitative gear pump). Further, the doping solution is cast from the crack of the press mold at the casting position of the endless metal support which is infinitely conveyed (for example, a stainless steel belt, or a rotating metal drum, etc.).

The shape of the crack of the mold base portion can be adjusted to facilitate the uniformity of the film thickness. For the press mold, there are a hanger type mold or a T mold, etc., which are preferably used. The surface of the metal support becomes a mirror surface. In order to increase the film forming speed, two or more pressurizing dies are provided on the metal support, and the flow rate of the doping solution can be laminated. The film of the laminated structure can be obtained by a co-casting method in which a plurality of doping solutions are simultaneously cast.

3) Solvent evaporation. Stripping step

The doped solution cast on the metal support is heated on the metal support to evaporate the solvent in the doping solution to obtain a film.

Evaporating the solvent, although there is a method of blowing the wind from the side of the doping solution side and/or a method of transferring heat from the liquid in the support body, a method of transferring heat from the surface by radiant heat, etc. Good drying efficiency is preferred. Further, it is preferable to use a combination of the methods. The doping solution on the metal support is preferably dried on the support in an atmosphere in the range of 40 to 100 ° C. Maintained in the range of 40~100 °C In an atmosphere, it is preferred to contact the warm air of this temperature with the surface of the doping solution on the metal support or by means of infrared rays or the like.

The film obtained by evaporating the solvent on the metal support was peeled off at the peeling position. From the viewpoint of surface quality, moisture permeability, and peelability of the obtained film, it is preferred that the film is peeled off from the metal support within 30 to 120 seconds after casting. The temperature at the peeling position on the metal support is preferably in the range of 10 to 40 ° C, more preferably in the range of 11 to 30 ° C.

The amount of the residual solvent at the time of peeling off the film on the metal support at the time of peeling is preferably 50 to 120% by mass in terms of the strength of the drying conditions and the length of the metal support. However, when the amount of the residual solvent is more, the film is too soft, and the film is damaged when it is too soft, and the peeling tension is likely to cause displacement or vertical streaks. Therefore, considering the economic speed and quality, the amount of residual solvent at the time of peeling is determined.

The residual solvent amount of the film is defined by the following formula.

Residual solvent amount (%) = (mass before heat treatment of film material - mass after heat treatment of film) / (mass after heat treatment of film) × 100

In addition, the heat treatment in the case of measuring the amount of residual solvent is a heat treatment performed at 140 ° C for 1 hour.

The peeling tension at the time of peeling off the metal support and the film is usually in the range of 196 to 245 N/m, and when wrinkles are likely to occur during peeling, it is preferable to peel at a tension of 190 N/m or less.

4) Drying and stretching steps

The peeled film is dried while being conveyed in a plurality of rolls placed in a drying apparatus. Further, in the tenter stretching device, both ends of the film are conveyed while being caught by a clip, and the film is stretched.

Drying is generally a method in which hot air is contacted on both sides of the film, but it can be replaced by microwave heating instead of hot air. Too much urgency is easy to damage the flatness of the film that has just been completed. It may be carried out after drying at a high temperature and the residual solvent is about 8% by mass or less. By the whole, the drying is carried out in the range of about 40 to 250 °C. In particular, it is preferred to dry it in the range of 40 to 200 ° C.

When the tenter stretching device is used for drying, the drying temperature is preferably in the range of 30 to 160 ° C, and more preferably in the range of 50 to 150 ° C. In the tenter stretching device, although the temperature distribution in the lateral direction of the atmosphere is small, it is preferable from the viewpoint of improving the uniformity of the film. Therefore, the temperature distribution in the transverse direction of the tenter step is preferably within ±5 ° C, more preferably within ± 2 ° C, and optimal within ± 1 ° C.

In order to obtain the optical film of the present invention, the stretching is preferably carried out in at least two directions (biaxial stretching). The biaxial stretching is preferably performed in the casting direction (MD direction) and the lateral direction (TD direction). The two-axis extension can be carried out simultaneously and can be carried out in stages.

The so-called phase, for example, can be extended in different extension directions in sequence, multi-stage extension of the same direction, and extension of different directions can be added to any of its stages. For example, it may be an extension step as follows.

Extending in the casting direction → extending in the lateral direction

Extending in the lateral direction → extending in the lateral direction

Extending in the casting direction → extending in the lateral direction → extending in the lateral direction

Extending in the transverse direction → extending in the lateral direction → extending in the casting direction

At the same time, the two-axis extension extends in one direction, and also includes the case where the other side is relaxed and contracted.

The stretching ratio can be set to be 2.5 to 9 times the total of the stretching ratios in the casting direction (MD direction) and the lateral direction (TD direction), preferably 3 to 6 times, more preferably 3.2 to 6 times. Specifically, the stretching ratio in the casting direction (MD direction) and the lateral direction (TD direction) may be 1.3 to 4.0 times, preferably 1.5 to 3.0 times, respectively. For example, the stretching ratio in the casting direction (MD direction) may be 2.0 times, the stretching ratio in the lateral direction (TD direction) may be 1.5 times, and the total of the stretching ratios is 2.0 + 1.5 = 3.5 times.

As described above, a film containing a cellulose ester in which all of the mercapto groups are an ethyl acetate group and an additive having a ring structure has high elongation. Therefore, the optical film obtained by biaxially stretching the film at a high magnification is less likely to cause white turbidity, and the tensile elastic modulus in both directions perpendicular to each other is high, and the elongation at break is lowered.

The residual solvent amount of the film at the start of stretching is preferably in the range of 20 to 100% by mass. The film obtained after the end of the stretching is preferably dried until the amount of the residual solvent is 5% by mass or less, preferably 1% by mass or less.

5) Rolling step

The optical film obtained after stretching and drying was wound into a roll by a coiler. The winding method can be used by a general user, and there are a constant torque method, a constant tension method, a taper tension method, and a program tension control method in which internal stress is constant, and the like can be used separately.

The optical film of the present invention may be a long-length film. For example, the length may be from about 100 m to 10,000 m, and the width may be from 1 to 4 m, preferably from 1.4 to 3 m. The long-length film is usually stored in a roll body that is wound in a vertical direction with respect to the width direction.

Before the winding, the width of the product is cut, and after cutting the end portion in the width direction of the optical film, the knurl processing (embossing processing) can be further performed in order to prevent sticking or scratching of the inner surface of the roll. Both ends in the width direction. The method of ridge processing can be processed by heating or pressurizing a metal ring having a convex-concave pattern on the side.

The optical film of the present invention has a tensile modulus which is improved as described above. Therefore, even when the thickness of the film is as small as 15 to 35 μm, when the core body is horizontally stored, deformation of the center portion in the width direction of the film due to its own weight (change in the winding shape) can be suppressed.

3. Polarizer

The polarizing plate of the present invention has a polarizing film and an optical film of the present invention disposed on at least one side thereof.

The polarizer is an element that passes only the light of the deflecting surface in a certain direction, and is, for example, a polyvinyl alcohol-based polarizing film. In the polyvinyl alcohol-based polarizing film, it is used to dye iodine on a polyvinyl alcohol-based film, and to make two colors Sex dye dyes.

The polarizer is subjected to dyeing after one-axis stretching of the polyvinyl alcohol film, or after dyeing the polyvinyl alcohol film, and is preferably subjected to one-axis stretching, preferably by further durability treatment with a boron compound. The film thickness of the polarizer is preferably in the range of 5 to 30 μm, more preferably in the range of 5 to 15 μm.

The polyvinyl alcohol film is preferably used in an amount of from 1 to 4 mol%, a polymerization degree of from 2000 to 4000, and a degree of saponification as described in JP-A-2003-248123, JP-A-2003-342322, and the like. 99.0~99.99 mol% of ethylene modified polyvinyl alcohol.

When the optical film of the present invention is disposed on the surface on the side of the polarizer, a retardation film can be disposed on the other side of the polarizer. The retardation of the retardation film can be set in accordance with the type of the liquid crystal cell to be combined. For example, the retardation film has an in-plane retardation Ro (590) measured at 23 ° C RH 55% and a wavelength of 590 nm in a range of 30 to 150 nm, and a retardation Rth (590) in a thickness direction is preferably in the range of 70 to 300 nm. For the retardation film having the retardation in the above range, for example, a VA liquid crystal cell or the like can be preferably used.

The bonding of the optical film and the polarizer is not particularly limited, but it can be carried out using a fully alkalized polyvinyl alcohol-based adhesive or an active energy ray-curable adhesive. It is preferable to use an active energy ray-curable adhesive from the viewpoint that the obtained adhesive layer has a high modulus of elasticity and it is easy to suppress the deformation point of the polarizing plate.

As a preferred example of the active energy ray-curable adhesive, as disclosed in JP-A-2011-028234, it is exemplified that it contains (α) cationic poly a conjugated compound, a (β) photocationic polymerization initiator, a photocurable adhesive which exhibits a maximum absorption of light at a wavelength longer than 380 nm, and a photosensitive agent of (δ) naphthalene-based photosensitizer Composition. However, it is also possible to use a light curable adhesive other than the above.

Hereinafter, an example of a method of producing a polarizing plate using a photocurable adhesive will be described. The polarizing plate may be coated with the following photohardenability by including: 1) a surface which is followed by a polarizer of the optical film; and 2) at least one side of the photoconductor and the bonding surface of the optical film. The adhesive application step of the adhesive agent, 3) the step of bonding the polarizer and the optical film through the obtained adhesive layer, and 4) hardening by bonding the polarizer and the optical film through the adhesive layer It is then manufactured by the manufacturing method of the hardening step of the agent layer. 1) The previous processing steps can be carried out if necessary.

(pre-processing steps)

In the pre-treatment step, the subsequent processing of the optical film with the polarizer is facilitated. When the optical film is respectively adhered to both sides of the polarizer, it is easy to carry out subsequent processing on the bonding surface of the individual optical film and the polarizer. Examples of the easy subsequent treatment include corona treatment, plasma treatment, and the like.

(adhesive coating step)

In the adhesive application step, the photocurable adhesive is applied to at least one of the surface of the polarizer and the optical film. When a direct photocurable adhesive is applied to the surface of a polarizer or an optical film, the coating method is not particularly limited. For example, a doctor blade type, a wire bar type, a die coater, and a double roll can be used. Various coating methods such as barrel coating and gravure coating machine. Further, after casting the photocurable adhesive between the polarizer and the optical film, it may be pressed by a roller or the like to be uniform.

(Fitting step)

After the photocurable adhesive is applied in this manner, it is supplied to the bonding step. In this bonding step, for example, when a photocurable adhesive is applied to the surface of the polarizer in the previous coating step, the optical film is laminated thereon. When a photocurable adhesive is applied to the surface of the optical film in the previous coating step, a polarizer is laminated thereon. Further, when a photocurable adhesive is cast between the polarizer and the optical film, the polarizer and the optical film are laminated in this state. When the optical film is applied to both surfaces of the polarizer, when a photocurable adhesive is used on both surfaces, the optical film is laminated on both surfaces of the polarizer through the photocurable adhesive. In this state, in general, when the optical film is laminated on one side of the polarizer, when the optical film is laminated on both the polarizer side and the optical film side and on both sides of the polarizer, the optical film side on both sides is rolled by a roller or the like. Live and pressurize. The material of the roller can be metal or rubber. Configure the rollers on both sides, which can be the same material and can be made of different materials.

(hardening step)

In the hardening step, the active energy ray is irradiated to the uncured photocurable adhesive to harden the adhesive layer containing the epoxy compound or the propylene oxide compound. Thereby, the laminated polarizers are bonded to the optical film through the photocurable adhesive. Active energy when bonding an optical film to a single side of a polarizer The line can be illuminated from either the polarizer side or the optical film side. Further, when the optical film is bonded to both surfaces of the polarizer, the optical fiber film is irradiated with the photocurable adhesive on both sides of the polarizer, and the active energy ray is irradiated from the side of the optical film on either side, and the light on both sides is hardened. It is advantageous to harden the adhesive.

As the active energy ray, visible light, ultraviolet light, X-ray, electron beam, or the like can be used because the operation is easy and the curing speed is sufficient. Generally, it is preferable to use an electron beam or an ultraviolet ray.

If the irradiation condition of the electron beam is a condition capable of curing the above-mentioned adhesive, any appropriate conditions can be employed. For example, electron beam irradiation, the acceleration voltage is preferably in the range of 5 to 300 kV, more preferably in the range of 10 to 250 kV. When the accelerating voltage is less than 5kV, the electron beam does not reach the adhesive and causes insufficient hardening. When the accelerating voltage exceeds 300kV, the electron beam rebounds due to the excessive penetration of the sample, which is caused by the transparent optical film or polarizer. The flaw of injury. The irradiation line amount is in the range of 5 to 100 kGy, preferably in the range of 10 to 75 kGy. When the amount of irradiation line is less than 5 kGy, the adhesive becomes insufficiently hardened. When it exceeds 100 kGy, damage occurs in the transparent optical film or the polarizer, and mechanical strength is lowered or yellowed, and predetermined optical characteristics are not obtained.

The ultraviolet irradiation condition may be any suitable condition if it is a condition capable of curing the above-mentioned adhesive. The amount of ultraviolet light irradiation is preferably in the range of 50 to 1,500 mJ/cm ² of the cumulative light amount, and more preferably in the range of 100 to 500 mJ/cm ² .

The polarizing plate obtained as described above, the adhesive Although the thickness of the layer is not particularly limited, it is usually in the range of 0.01 to 10, preferably in the range of 0.5 to 5 μm.

As described above, the optical film of the present invention has a reduced elongation at break in the direction of the slow axis and the direction perpendicular thereto. Therefore, it is considered that the polarizing plate including the optical film of the present invention is hard to generate heat wrinkles even under high temperature and high humidity.

4. Liquid crystal display device

The liquid crystal display device of the present invention comprises a liquid crystal cell and a pair of polarizing plates. Further, at least one of a pair of polarizing plates can be used as a polarizing plate comprising the optical film of the present invention. At least one of the polarizing plates has a polarizer and an optical film of the present invention. The optical film of the present invention is preferably disposed on the surface opposite to the liquid crystal cell of the polarizer (which is disposed as F1 or F4 to be described later).

Fig. 1 is a schematic view showing an example of a basic configuration of a liquid crystal display device. As shown in FIG. 1, the liquid crystal display device 10 of the present invention includes a liquid crystal cell 30, a first polarizing plate 50, a second polarizing plate 70, and a backlight 90.

For the liquid crystal cell 30, for example, various display modes such as STN, TN, OCB, HAN, VA (MVA, PVA), and IPS have been proposed. In order to obtain high contrast, the VA (MVA, PVA) mode is preferred.

The VA liquid crystal cell has a pair of transparent substrates and a liquid crystal layer sandwiched between them.

Among the pair of transparent substrates, the transparent substrate on one side is A pixel electrode is disposed by applying a voltage to the liquid crystal molecules. The counter electrode may be disposed on the transparent substrate on the one side (the pixel electrode is disposed), or may be disposed on the other transparent substrate, and the transparent substrate may be disposed on the one side (the pixel electrode is disposed) in order to increase the aperture ratio. It is better.

The thickness of the transparent substrate is preferably in the range of 0.3 to 0.7 mm, more preferably in the range of 0.3 to 0.5 mm.

The liquid crystal layer contains liquid crystal molecules having negative or positive dielectric anisotropy. It is preferable to arrange the pixel electrode on the transparent substrate on one side and the liquid crystal molecule having the negative dielectric anisotropy when the opposite electrode is disposed on the transparent substrate on the other side. When the pixel electrode and the counter electrode are disposed on one side of the transparent substrate, liquid crystal molecules having positive dielectric anisotropy are preferred. The alignment control force of the alignment film of the liquid crystal molecules on the surface of the liquid crystal layer side of the transparent substrate, when no voltage is applied (when an electric field is not generated between the pixel electrode and the counter electrode), the long axis of the liquid crystal molecules is opposite to the transparent substrate The surface is aligned in a slightly vertical manner.

In the liquid crystal cell thus constituted, an electric field is generated between the pixel electrode and the counter electrode by applying an image signal (voltage) to the pixel electrode. Thereby, the liquid crystal molecules which are initially aligned with respect to the surface of the transparent substrate are aligned so that the long axis thereof is horizontal with respect to the substrate surface. In this manner, the liquid crystal layer is driven, and the transmittance and reflectance of each sub-pixel are changed to display the image.

The first polarizing plate 50 includes a first polarizer 51, a protective film 53 (F1) disposed on the surface on the viewing side of the first polarizer 51, and a protective film disposed on the liquid crystal cell side of the first polarizer 51. 55 (F2). The second polarizing plate 70 includes a second polarizer 71, a protective film 73 (F3) disposed on the liquid crystal cell side of the second polarizer 71, and a protective film disposed on the backlight side of the second polarizer 71. 75 (F4). One side of the protective film 55 (F2) and the protective film 73 (F3) is sometimes omitted if necessary.

Further, at least one of the protective film 53 (F1) and the protective film 75 (F4) is preferably used as the optical film of the present invention.

As described above, the optical film of the present invention has less white turbidity and a reduced haze value. Therefore, the liquid crystal display device of the present invention having the optical film of the present invention as the protective film F1/F4 can have high luminance.

[Examples]

Hereinafter, the present invention will be specifically described by way of examples, but the present invention is not limited thereto.

1. Optical film material 1) Cellulose ester

The cellulose esters of the following tables were used.

2) Additives 2-1) Additives with ring structure

Polyester Compound 1: End-unsealant of a condensate (weight average molecular weight 2000, bulk index 0.23) composed of succinic acid/terephthalic acid/ethylene glycol (50/50/100 molar ratio)

The bulk index of the polyester compound 1 was calculated by the following method. That is, the polyester compound 1 contains: condensing unit of terephthalic acid/ethylene glycol-[C(=O)-C ₆ H ₄ -C(=O)-O-CH ₂ CH ₂ -O] - (molecular weight 192) 50, succinic acid / ethylene glycol condensation unit - [C (= O) - CH ₂ CH ₂ - C (= O) - O - CH ₂ CH _{2 -} O] - (molecular weight 144) 50. Therefore, the molecular weight of the polyester compound 1 is 192 × 50 + 144 × 50 + 18 = 16818. Further, the total molecular weight of the aromatic ring structure (-C ₆ H ₄ -) in the polyester compound 1 was 76 (molecular weight of -C ₆ H ₄ -) × 50 (pieces) = 3,800. Thus, the bulking index of the polyester compound 1 was 3800/16818 = 0.23.

Polyester compound 2: terminal unsealed product of condensate (weight average molecular weight 600) composed of succinic acid/terephthalic acid/ethylene glycol (50/50/100 molar ratio)

Polyester compound 3: terminal unsealed product of condensate (weight average molecular weight 3000) composed of succinic acid/terephthalic acid/ethylene glycol (50/50/100 molar ratio)

Polyester compound 4: terminal unsealed product of condensate (weight average molecular weight 2000) composed of succinic acid/terephthalic acid/ethylene glycol (80/20/100 molar ratio)

Polyester compound 5: terminal unsealed product of condensate (weight average molecular weight 2000) composed of succinic acid/terephthalic acid/ethylene glycol (75/25/100 molar ratio)

Polyester compound 6: benzoic acid sealant of condensate (weight average molecular weight 400) composed of adipic acid/phthalic acid/propylene glycol (50/50/100 molar ratio)

Polyester compound 7: benzoic acid sealant of condensate (weight average molecular weight 2000) composed of succinic acid/terephthalic acid/ethylene glycol (75/25/100 molar ratio)

Polyester compound 8: terminal unsealed condensate (weight average molecular weight 1000) composed of adipic acid/terephthalic acid/propylene glycol (50/50/100 molar ratio)

Polyester compound 9: terminal unsealed product of condensate (weight average molecular weight 1000) composed of sebacic acid/terephthalic acid/ethylene glycol (50/50/100 molar ratio)

Styrene compound 1: Sartomer, SMA2625 (styrene/maleic anhydride (67/33 molar ratio) copolymer, weight average molecular weight 9000, bulk index 0.82)

The bulk index of the styrene compound 1 was calculated by the following method. That is, the styrene-based compound 1 contains 67 units of styrene unit-CH(C ₆ H ₅ )-CH ₂ - (molecular weight 104) and maleic anhydride unit-C ₂ H ₂ (C ₂ O ₃ )-( The molecular weight is 98)33. Thus, the molecular weight of the styrene-based compound 1 was 104 × 67 + 98 × 33 + 2 = 10,204. Further, in the styrene compound 1, the total ring structure derived from styrene (-C ₆ H ₅ ) and the non-aromatic ring structure derived from maleic anhydride (-CHC(=O)OC(=O)CH-) The molecular weight was 77 (molecular weight of -C ₆ H ₅ ) × 67 (pieces) + 98 (molecular weight of -CHC(=O)OC(=O)CH-) × 33 (pieces) = 8393. Thus, the bulking index of the styrene-based compound 1 was 8393/10204=0.82.

Styrene compound 2: manufactured by Maruzen Petrochemical Co., Ltd., Markalinker CST50 (styrene/hydroxystyrene (50/50 molar ratio) copolymer, weight average molecular weight 2000, bulk index 0.76).

The bulk index of the styrene compound 2 was calculated by the following method. That is, the styrene-based compound 2 contains 50 units of styrene unit-CH(C ₆ H ₅ )-CH ₂ - (molecular weight 104), and hydroxystyrene unit-CH(C ₆ H ₅ OH)-CH ₂ - (molecular weight 120) 50. Thus, the molecular weight of the styrene-based compound 2 is 120 × 50 + 104 × 50 + 2 = 11202. Further, the total molecular weight of the aromatic ring structure -C ₆ H ₅ /-C ₆ H ₅ OH in the styrene compound 2 is 77 (molecular weight of -C ₆ H ₅ ) × 50 (pieces) + 93 (-C ₆ Molecular weight of H ₅ OH) × 50 (pieces) = 8500. Thus, the bulking index of the styrene-based compound 2 was 8500/11202 = 0.76.

Sugar ester compound 1: a sugar ester compound represented by the following formula (3)

R ₁ ~ R ₈ : benzylidene (average degree of substitution: 5.5), residual hydrogen atom

Sugar ester compound 2: a sugar ester compound in which the average degree of substitution of the benzamidine group of R ₁ to R _{8 in} the above formula (3) is changed to 6.5

Sugar ester compound 3: the average degree of substitution of the benzamidine group of R ₁ to R _{8 in} the above formula (3) is changed to a sugar ester compound of 7.2

Sugar ester compound 4: a sugar ester compound in which the average degree of substitution of the benzamidine group of R ₁ to R _{8 in} the above formula (3) is changed to 8.0

2-2) Other additives

Polyester compound A: terminal unsealed product of condensate (weight average molecular weight 1700) composed of adipic acid/ethylene glycol

TPP: triphenyl phosphate

BDP: biphenyl diphenyl phosphate

2. Production of optical film (Example 1)

The following components are fully dissolved while stirring and heating, and prepared Doping solution.

(composition of doping solution)

Cellulose ester A1: 100 parts by mass

Polyester compound 1: 10 parts by mass

UV absorber: Ti928: 2-(2H-benzotriazol-2-yl)-6-(1-methyl-1-phenylethyl)-4-(1,1,3,3-tetramethyl Butyl) phenol (TINUVIN 928, manufactured by BASF Japan): 3.0 parts by mass

Matting agent: R972V (manufactured by Nippon Aerosil Co., Ltd., cerium oxide particles, average particle diameter = 16 nm): 0.30 parts by mass

Peeling aid: ELECUTS412 (made by Takemoto Oil Co., Ltd.): 0.50 parts by mass

Dichloromethane: 300 parts by mass

Ethanol: 40 parts by mass

The obtained dope solution was uniformly cast into a stainless steel belt support at a temperature of 22 ° C and a width of 2 m using a belt casting apparatus. The amount of residual solvent was made to be a solvent in the 100% evaporation doping solution on the stainless steel belt support. Further, the obtained film was peeled off from the stainless steel belt support at a peeling tension of 162 N/m.

Next, the peeled film was further dried at 35 ° C and then cracked to a width of 1 m. The obtained film was stretched by 2.0 times in the conveyance direction (MD direction) at 200 ° C between rolls, and extended by 1.5 times in the transverse direction (TD direction) at 200 ° C in a tenter. The amount of residual solvent at the start of the extension caused by the tenter was 8%.

After stretching by a tenter, the film was subjected to a relaxation treatment at 130 ° C for 5 minutes, and the obtained film was dried while being conveyed by a plurality of rolls in a drying zone of 120 ° C and 140 ° C. The obtained film was spun into a width of 1.5 m, and embossed by a width of 10 mm and a height of 5 μm at both ends in the width direction of the film, and wound into a core shape. Thereby, the roll body of the optical film 101 is obtained. The optical film 101 has a film thickness of 25 μm and a roll length of 4000 m.

(Examples 2 to 36, Comparative Examples 1 to 6 and 8 to 11)

The optical film 102 was obtained in the same manner as in Example 1 except that the cellulose ester, the additive, the content thereof, the stretching conditions, and the film thickness were changed to the ones shown in Table 3 or 4. ~142 and 144~147.

(Comparative Example 7) Manufacture of particles

The cellulose ester C (cellulose acetate propionate) of Table 1 was dried at 90 ° C for 6 hours or more in a dehumidifying hot air dryer to set the water content to 80 ppm or less. The obtained cellulose ester C and the following additives were mixed in a hopper to form a resin composition.

(composition of resin composition)

Cellulose ester C: 100 parts by mass

Polyester compound 1: 10 parts by mass

GSY-P101 (manufactured by Dai Chemical Industry Co., Ltd.): 0.25 parts by mass

Irganox1010 (made by BASF Japan Co., Ltd.): 0.5 parts by mass

SumilizerGS (manufactured by Sumitomo Chemical Co., Ltd.): 0.24 parts by mass

R972V (manufactured by Aerosil Co., Ltd.): 0.15 parts by mass

The above resin composition was placed in a twin-screw extruder for melt-kneading. The hole provided in the front of the crystal grain was opened to a metal mesh (filter portion) of 100 μm, and the molten resin was filtered, and then extruded at a temperature of 240 ° C from a circular diameter of the crystal grain to form a chain. After the extruded molten resin was water-cooled, a cylindrical shape having a diameter of 5 mm and a cross-sectional diameter of 2.5 mm was cut by a steel wire cutter to obtain pellets.

Film manufacturing

The obtained pellets were dried at 90 ° C for 6 hours under reduced pressure, and then placed in a single-screw extruder. Further, after melt-kneading at 240 ° C in a nitrogen atmosphere, it was extruded from a die to a cooling roll having a surface temperature of 90 °C. The extruded resin was cooled and solidified by a plurality of cooling rolls, and then peeled off with a peeling roll to obtain a film. The two ends of the obtained film were cracked by 10 cm, and the film direction of the roll stretching device (MD direction) was extended at 200 ° C to a stretching ratio of 2.0 times in the transverse direction of the tenter (TD). The direction) is extended 1.5 times at 200 °C. An optical film 143 having a film thickness of 25 μm was obtained in the same manner as in Example 1 except the above.

The composition and elongation conditions of the optical films of Examples 1 to 19 and Comparative Examples 1 to 3 are shown in Table 3; the compositions and extension conditions of the optical films of Examples 20 to 36 and Comparative Examples 4 to 11 are shown in Table 4.

The tensile modulus, the elongation at break, the haze value, R ₀ and Rth, and the wound shape of the obtained optical film were measured by the following methods.

[Tensile modulus and elongation at break]

First, the optical film was cut into a size of 10 mm (MD direction) × 100 mm (TD direction) to obtain a sample film. The sample film was conditioned for 24 hours at 25 ° C, 55% RH. The sample film after the humidity control was subjected to Tensilon RTC-1225A manufactured by Orientec Co., Ltd. according to JIS K7127, and the distance between the chucks was set to 50 mm, and the film was stretched in the MD direction, and the tensile modulus and the elongation at break in the MD direction were measured. Further, the tensile modulus and the elongation at break in the TD direction were measured in the same manner except that the direction of the stretched sample film was changed to the TD direction. The tensile modulus and the elongation at break were measured under the conditions of 23 ° C, 55% RH, and a tensile speed of 50 mm/min.

[fog value]

The obtained optical film was conditioned at 23 ° C and 55% RH for 5 hours or more. Next, the obtained optical film has a haze value according to JIS K-7136 at 23 ° C and 55% RH in a haze meter (turbidity meter) (type: NDH 2000, Nippon Electric Co., Ltd.) ) Determination.

[R ₀ and Rth]

The retardation R _{0 in} the in-plane direction of the optical film and the retardation Rth in the thickness direction were measured by the following methods.

1) The optical film was conditioned at 23 ° C, 55% RH. The average refractive index of the optical film after the humidity adjustment was measured by an Abbe refractometer.

2) The optical film after the humidity control is measured such that R ₀ at the time of incidence of light at a wavelength of 590 nm parallel to the normal of the surface of the film is measured by KOBRA 21DH and prince measurement.

3) From KOBRA21ADH, the slow phase axis in the plane of the optical film is used as the tilt axis (rotation axis), and the normal to the surface of the optical film is measured from the angle θ (incident angle (θ)) to the light having a wavelength of 590 nm. The time delay value R(θ). The measurement of the retardation value R(θ), θ is in the range of 0° to 50°, and is measured at 6 points every 10°. The retardation axis in the plane of the optical film was confirmed by KOBRA21ADH.

4) From the measured R ₀ and R (θ), and the average refractive index and film thickness described above, nx, ny, and nz were calculated from KOBRA21ADH, and Rth at a measurement wavelength of 590 nm was calculated.

[Change in winding shape]

A roll body (winding length: 4000 m, width: 1330 m) in which the optical film was wound in the vertical direction with respect to the width direction was prepared. The roll body is covered with a polyethylene sheet for preventing dust from adhering, and stored in a warehouse at 30° C. to 40° C. and 65% RH to 85% RH for one month so that the length of the core (core) is horizontal. Then, the wound state of the roll body after one month passed was visually observed and evaluated as follows.

◎: No change in wrinkles, deformation, etc. on the surface of the roller

○: Although the surface of the roller is only slightly wrinkled, it is not considered to be deformed.

△: A slight wrinkle was found on the surface of the roller, and some deformation was also confirmed.

×: On the surface of the roll, there are strong wrinkles inside and strong fission on the surface. Shape, deformation to the inside

The evaluation results of the optical films of Examples 1 to 19 and Comparative Examples 1 to 3 are shown in Table 5; and the evaluation results of the optical films of Examples 20 to 36 and Comparative Examples 4 to 11 are shown in Table 6.

As shown in Tables 5 and 6, it is understood that the elongation at break in the MD direction/TD direction of the films of Examples 1 to 36 is in the range of 1 to 10%, and the haze value is as low as 1% or less, and the winding shape is changed. less. For this, it is understood that the film of Comparative Examples 1 to 9 is at least one side of the MD direction/TD direction. The elongation at break is higher than 10%, and the change in the winding shape is large.

Specifically, it was found that the film of Comparative Example 1 contained white turbidity and high elongation at break because it contained CAP having relatively high flexibility. It was found that the film of Comparative Example 2 was too low in elongation at break because the stretching ratio was too high. The film of Comparative Example 4 was not extended, and the film of Comparative Example 5 was only extended in the TD direction, and the film of Comparative Example 6 was extended at a low magnification in both MD/TD directions, and it was found that the elongation at break was high. In the film of Comparative Example 7, since a molten film-forming film of CAP was used, it was found that not only white turbidity but also elongation at break was high. The TPP/BDP contained in the films of Comparative Examples 9 and 11 easily bleed out, and it was found that since the content in the film in the film forming step was reduced, the elongation was low, and the elongation at break of the film after stretching was also high. In Comparative Examples 8 and 10, it was found that the film had low elongation and was broken under the extension conditions shown in Table 4.

3. Production of phase difference film

1) Phase difference film a

The doping solution 1 was prepared by sufficiently dissolving the following components while stirring and heating.

(composition of doping solution 1)

Cellulose ester (ethylene ethyl phthalate substitution degree 2.3, weight average molecular weight Mw 185,000 diethylene fluorenyl cellulose): 100 parts by mass

The following compound A-022 (slow riser): 4 parts by mass

A sugar ester compound represented by the following formula (5): 10 parts by mass

R972V (manufactured by Nippon Aerosil Co., Ltd., cerium oxide particles, average particle diameter = 16 nm, matting agent): 0.30 parts by mass

Dichloromethane: 300 parts by mass

Ethanol: 40 parts by mass

R ₁ ~ R ₈ : methylcarbonyl (CH ₃ CO-), average degree of substitution: 5.5 residual as a hydrogen atom

The dope solution 1 prepared as described above was uniformly cast into a 2 m-wide stainless steel belt support at a temperature of 22 ° C using a belt casting apparatus. The solvent in the dope solution 1 of the stainless steel belt support evaporates the residual solvent amount to 100%, and then peels off from the stainless steel belt support at a peeling tension of 162 N/m. The film was obtained. Next, the solvent in the obtained film was further evaporated at 35 ° C, and then cracked to a width of 1 m. The obtained film was stretched by 1.1 times in the transport direction (MD direction) in the region, and stretched in a lateral direction (TD direction) of 1.5 times with a tenter, and dried at a drying temperature of 135 °C. The amount of residual solvent at the start of the extension caused by the tenter was 8%. After the extension of the tenter, the relaxation treatment was carried out at 130 ° C for 5 minutes.

The obtained film was dried while being conveyed by a plurality of rolls in a drying zone of 120 ° C and 140 ° C to be dried. Then, the film was cracked to a width of 1.5 m, and embossing was performed at a width of 10 mm and a height of 5 μm at both end portions in the width direction of the film to obtain a retardation film a having a film thickness of 30 μm.

2) retardation film b

Modulation of doping solution

The following components were mixed to prepare doping solutions A and B, respectively.

(composition of doping solution A)

Cellulose ester CE-1 (degree of substitution of ethanethiol 2.81, total substitution of sulfhydryl 2.81): 100 parts by mass

Additive A-5: terephthalic acid/succinic acid (55 mol% / 45 mol%) / ethylene glycol / propylene glycol (45 mol% / 55 mol%) acetic acid end seal (number average molecular weight 800 ): 12 parts by mass

The following compound A: 4 parts by mass

Matting agent dispersion (AEROSIL R972, Japan AEROSIL shares Co., Ltd., 2 times average particle size of 1.0 μm or less): 0.13 parts by mass relative to 100 parts by mass of the cellulose ester

Dichloromethane: 406 parts by mass

Methanol: 61 parts by mass

(composition of doping solution B)

Cellulose ester CE-2 (degree of substitution of ethyl ketone 2.43, total substitution of thiol 2.43): 100 parts by mass

Additive A-5: terephthalic acid/succinic acid (55 mol% / 45 mol%) / ethylene glycol / propylene glycol (45 mol% / 55 mol%) acetic acid end seal (number average molecular weight 800 ): 18 parts by mass

Matting agent dispersion (AEROSIL R972, manufactured by AEROSIL Co., Ltd., 2 times average particle size: 1.0 μm or less): 0.13 parts by mass relative to 100 parts by mass of the cellulose ester

Dichloromethane: 406 parts by mass

Methanol: 61 parts by mass

(co-cast film)

The obtained doping solutions A and B were simultaneously subjected to multilayer casting on the running casting bar in the order of lamination from the casting mold to the doping solution A/doping solution B/doping solution A. The amount of casting of each doping was adjusted so that the core layer (layer of the doping solution B) became the thickest. A film in which the amount of residual solvent was peeled off from the cast rod at about 30% by mass was applied, and a hot air of 140 ° C was applied by a tenter to extend 30% in the width direction. Then, it is transferred from the tenter to the roll transfer, and further dried from 120 ° C to 150 ° C to obtain a retardation film b. The film thickness of the obtained retardation film b, the surface layer (layer of the doping solution A) / the core layer (layer of the doping solution B) / the surface layer (layer of the doping solution A) was 2.5 μm / 55 μm / 2.5 μm.

3) retardation film c

The pellet of ZEONOR 1420 (manufactured by Zeon Co., Ltd.) of the decene-based resin was dried at 100 ° C for 5 hours. Then, the pellet was supplied to an extruder at a normal temperature and melted at 250 ° C, and discharged from a die onto a cooling drum to obtain an unstretched film having a thickness of 150 μm.

Next, the unstretched film was stretched 1.2 times in the longitudinal direction (MD direction) at a temperature of 143 ° C in a longitudinal stretching machine using a floating method between rolls. This was supplied to a horizontal stretcher using a tenter method, and the tensile tension and the tenter chain tension were adjusted while further extending to 1.8 times in the lateral direction (TD direction) at a temperature of 150 °C. Thereby, the retardation film c is obtained.

The retardation R _{0 in} the in-plane direction of the wavelength difference 590 nm of the obtained retardation films a to c and the retardation Rth in the thickness direction were measured in the same manner as described above. The evaluation results are shown in Table 7.

4. Production of polarizing plate (Example 37) 1) Modulation of polarized photons

A polyvinyl alcohol film having a thickness of 30 μm was swollen with water at 35 °C. The obtained film was immersed in an aqueous solution of 0.075 g of iodine, 5 g of potassium iodide and 100 g of water, and further immersed in an aqueous solution of 45 g of potassium iodide, 7.5 g of boric acid and 100 g of water. The obtained film was subjected to one-axis stretching under the conditions of an extension temperature of 55 ° C and a stretching ratio of 5 times. After the one-axis stretched film was washed with water, it was dried to obtain a polarizer having a thickness of 10 μm.

2) Modulation of photocurable adhesive

After mixing the following components, the mixture was defoamed to prepare a photocurable adhesive. Further, the triarylsulfonium hexafluorophosphate was blended into a 50% propylene carbonate solution, indicating that the solid content of the triarylsulfonium hexafluorophosphate was as follows.

(composition of photocurable adhesive)

3,4-epoxycyclohexylmethyl-3,4-epoxycyclohexanecarboxylate: 45 parts by mass

EPOLEADGT-301 (alicyclic epoxy resin manufactured by Daicel Chemical Co., Ltd.): 40 parts by mass

1,4-butanediol diglycidyl ether: 15 parts by mass

Triarylsulfonium hexafluorophosphate: 2.3 parts by mass

9,10-dibutoxyanthracene: 0.1 parts by mass

1,4-diethoxynaphthalene: 2.0 parts by mass

Polaroid production

The photocurable adhesive having the above-described prepared photocurable adhesive was applied to a dry thickness of 5 μm using a micro gravure coater to form a photocurable adhesive layer. The coating was carried out under the conditions of a gravure roll #300 and a rotation speed of 140%/linear velocity.

Similarly, the photocurable adhesive having the above-described prepared photocurable adhesive was applied to a thickness of 5 μm on the optical film 101 to form a photocurable adhesive layer.

The retardation film a on which the photocurable adhesive layer is formed is disposed on the surface on which the phototransformer is formed, and the optical film 101 on which the photocurable adhesive layer is formed on the other surface to form a retardation film a/light. A laminate of a hardenable adhesive layer/photopolarizer/photocurable adhesive layer/optical film 101. The resulting laminate was applied as a roll. The bonding is performed such that the slow axis of the optical film 101 and the absorption axis of the polarizer are perpendicular to each other.

The polarizing plate 201 is obtained by irradiating an electron beam from both sides of the bonded laminate to cure the photocurable adhesive layer. The linear velocity is 20 m/min, the acceleration voltage is 250 kV, and the illumination line amount is 20 kGy.

(Examples 38 to 72, Comparative Examples 12 to 22)

The polarizing plates 202 to 247 were obtained in the same manner as in Example 37 except that the types of the optical film and the retardation film were changed as shown in Table 8 or 9.

The heat wrinkles of the obtained polarizing plate were evaluated in the following manner.

[Hot wrinkles] After the obtained polarizing plate 201 was stored at 85 ° C and 95% for 168 hours, it was visually observed whether or not thermal wrinkles were generated.

◎: No hot wrinkles

○: Although there are a small amount of hot wrinkles, it is practically no problem.

×: A large number of hot wrinkles are produced

The evaluation results of the polarizing plates of Examples 37 to 55 and Comparative Examples 12 to 14 are shown in Table 8. The evaluation results of the polarizing plates of Examples 56 to 72 and Comparative Examples 15 to 22 are shown in Table 9.

As shown in Tables 8 and 9, it was found that the polarizing plates of Examples 37 to 72 did not generate heat wrinkles, or that there was no problem in practical use even if hot wrinkles were produced, and the polarizing lights of Comparative Examples 10 to 16 and 18 The board produces hot wrinkles. It is considered that the film constituting the polarizing plates of Examples 37 to 72 has a high tensile modulus at least in the TD direction (preferably both in the TD direction/MD direction). From Examples 51 and 52, and beyond In comparison with the examples, it is understood that the tensile modulus of elasticity in the TD direction of the optical film is higher than that in the MD direction, and the heat wrinkles of the polarizing plate can be reduced.

5. Production of liquid crystal display device (Example 73)

One of the two sides of the liquid crystal cell of a commercially available VA liquid crystal display device (SONY 40-type display KLV-40J3000) is peeled off and attached to the polarizing plate, and the above-mentioned polarized plate 201 is bonded to both sides of the liquid crystal cell. The liquid crystal display device 301 is obtained. The bonding of the polarizing plate 201 is performed so that the retardation film a described above becomes the liquid crystal cell side.

(Examples 74 to 108, Comparative Examples 23 to 33)

The liquid crystal display devices 302 to 347 were obtained in the same manner as in Example 73 except that the polarizing plate 201 bonded to both surfaces of the liquid crystal cell was changed to the one shown in Table 10 or 11.

The brightness of the obtained liquid crystal display device was measured by the following method.

[front contrast (brightness)]

The brightness in the normal direction of the display screen from the white display of the liquid crystal display device and the brightness in the normal direction of the display screen from the black display were measured using EZ-Contrast 160D manufactured by ELDIM Co., Ltd., respectively. The obtained value was calculated as a frontal contrast in accordance with the following formula. The brightness is measured at 23 ° C, Performed in a 55% RH environment.

Front contrast = (luminance of the white display measured from the normal direction of the display device) / (the brightness of the black display measured from the normal direction of the display device)

Further, the brightness of the liquid crystal display device was evaluated based on the following criteria.

◎: The front contrast is 1200 or more

○: The front contrast is 1000 or more and less than 1200

×: The front contrast is less than 1000

The evaluation results of the liquid crystal display devices of Examples 73 to 91 and Comparative Examples 23 to 25 are shown in Table 10; and the evaluation results of the liquid crystal display devices of Examples 92 to 108 and Comparative Examples 26 to 33 are shown in Table 11.

As shown in Tables 10 and 11, the liquid crystal display devices of Examples 73 to 108 were found to have higher brightness than the liquid crystal display devices of Comparative Examples 23 to 25, 29, 31 and 33. It is considered that the film of F1/F4 constituting the liquid crystal display devices of Examples 73 to 108 has less white turbidity and a low haze value.

Priority is claimed on Japanese Patent Application No. 2012-242742, filed on Jan. The application Please refer to the contents of the manual and the drawings for the contents of this manual.

[Industrial availability]

The optical film of the present invention provides a white turbidity, is less likely to generate heat wrinkles, and reduces deterioration of the wound shape when stored in a roll body. A liquid crystal display device including such an optical film can improve brightness.

Claims (10)

An optical film characterized by an elongation at break of 25 ° C in a retardation axis direction of a cellulose ester having a total substitution degree of a fluorenyl group of 2.0 to 3.0 and an oxime group of all ethylene groups. The elongation at break at 25 ° C in the direction perpendicular to the direction of the retardation axis is 1 to 10%, and the thickness is 15 to 35 μm. The optical film of claim 1, wherein the haze value measured in accordance with JIS K-7136 is 0.5 or less. The optical film of claim 1, wherein the optical film further contains an additive having a ring structure and a molecular weight of 10,000 or less. The optical film of claim 3, wherein the additive is a polyester compound or a styrene compound having a ring structure of a non-aromatic ring structure or an aromatic ring structure, or a pyranose structure or furan. A sugar structure, and the aforementioned sucrose structure or furanose structure is a sugar ester compound having a substituent including a non-aromatic ring structure or an aromatic ring structure. The optical film of claim 3, wherein the aforementioned ring is configured as an aromatic ring. The optical film according to claim 3, wherein the additive is a polyester compound having a molecular weight of 600 or more in an aromatic ring structure and a styrene compound having a molecular weight of 600 or more in a ring structure. The optical film of claim 3, wherein the content of the additive is from 5 to 30% by mass based on the cellulose ester. The optical film of claim 1, wherein the direction of the slow axis in the plane of the film is at least 23 ° C of at least one side of the direction perpendicular to the direction of the late phase axis, The tensile modulus at 55% RH is 5.0 to 8.0 GPa. The optical film of claim 1, wherein the elongation at break at 25 ° C in the direction of the slow axis of the film surface and the elongation at break at 25 ° C in the direction perpendicular to the direction of the slow axis are 1 to 5 %. The optical film of claim 1, wherein the retardation R ₀ (590) in the in-plane direction of the measurement wavelength of 590 nm at 23 ° C and 55% RH is 10 nm or less.