JP5912277B2 - Optical film, polarizer protective film, polarizing plate, and image display device - Google Patents

Description

  The present invention relates to a low retardation optical film which is a biaxially stretched film. The present invention also relates to a polarizer protective film, a polarizing plate and an image display device.

  In recent years, the market of flat panel image display devices such as liquid crystal display devices (LCD) has been expanding. An optical film is used for the image display device. Optical films are required not only to be transparent, but also to have optical characteristics that are strictly adjusted to correspond to the optical design of the image display device. One of the optical characteristics is a phase difference. For example, a polarizer protective film used for an LCD polarizing plate is required to have a phase difference close to zero. The polymer material used for the optical film generally exhibits birefringence based on a difference in refractive index between a direction along the main chain of the polymer and a direction perpendicular to the main chain. For this reason, an optical film with a small retardation which can be used for a polarizer protective film cannot be obtained simply by selecting a polymer material having high transparency.

  By using a polymer material having a small refractive index difference, an optical film having a small retardation can be obtained. Such a material is typically a cellulose derivative such as triacetylcellulose. However, an optical film made of a cellulose derivative has a large retardation in the thickness direction, and thus has a large birefringence with respect to incident light from an oblique direction. Such birefringence characteristics exhibited by the cellulose derivative degrade the viewing angle characteristics of image display devices, particularly large-screen image display devices that have recently been developed.

  Polymeric materials other than cellulose derivatives can be used for the polarizer protective film. Patent Document 1 (Japanese Patent Laid-Open No. 2000-206333) discloses a polarizer protective film comprising a biaxially stretched film of polymethyl methacrylate (PMMA). This polarizer protective film has a small retardation and features derived from PMMA, for example, good moldability, high surface hardness, high light transmittance, and low wavelength dependency.

Apart from this, as a polymer material that can be used for an optical film, a (meth) acrylic polymer having a ring structure in the main chain is known. A (meth) acrylic polymer having a ring structure in the main chain has a higher glass transition temperature (Tg) than a (meth) acrylic polymer having no ring structure in the main chain. High Tg realizes an optical film having excellent heat resistance. An optical film having excellent heat resistance can be easily placed close to a heat generating part such as a light source in an image display device, for example. The optical film having excellent heat resistance has various other practical advantages. Patent Document 2 (Japanese Patent Laid-Open No. 2007-31537) discloses an optical film comprising a copolymer of an N-substituted maleimide ring structure in which the substituent Ar ¹ is an aromatic group and a (meth) acrylate unit. To do. The optical film of Patent Document 2 is not a polarizer protective film, but exhibits a large in-plane retardation of up to 400 nm.

JP 2000-206333 A JP 2007-31537 A

  PMMA used in Patent Document 1 has intrinsic birefringence although it is small. For this reason, the polarizer protective film currently disclosed by patent document 1 shows the phase difference of the thickness direction produced by biaxial stretching. The retardation in the thickness direction deteriorates the viewing angle characteristics of the image display device including the polarizer protective film. In addition, the Tg of PMMA is as low as about 100 ° C. For this reason, it is actually difficult to use the polarizer protective film for an image display device that requires high heat resistance.

  On the other hand, the resin film comprising the copolymer having an N-substituted maleimide structure disclosed in Patent Document 2 is hard and flexible because the N-substituted maleimide structure is located in the main chain of the copolymer. poor. By stretching the resin film, mechanical properties such as strength and flexibility are improved, and the resin film can be used as an optical film. Actually, the optical film of Patent Document 2 is a stretched film. However, since birefringence derived from the N-substituted maleimide structure is generated by stretching, it is difficult to use as a polarizer protective film that requires a small phase difference close to zero.

  In addition, the mechanical characteristics of the resin film such as strength and flexibility are improved by biaxial stretching as compared with the case of performing uniaxial stretching. However, in biaxial stretching, the phase difference in the thickness direction is usually larger than in uniaxial stretching. In the polarizer protective film, it is desired that the retardation in the thickness direction as well as the in-plane retardation is as small as possible.

  An object of the present invention is to provide an optical film having a small retardation and high heat resistance while being a biaxially stretched film.

  The optical film of the present invention contains a (meth) acrylic polymer (c) having N-substituted maleimide units (a) and (meth) acrylic acid ester units (b) as constituent units. The N-substituted maleimide unit (a) is a structural unit having an action of imparting positive intrinsic birefringence to the (meth) acrylic polymer (c). The (meth) acrylic acid ester unit (b) is a structural unit having an action of giving negative intrinsic birefringence to the (meth) acrylic polymer (c). The in-plane retardation Re of the optical film of the present invention with respect to light having a wavelength of 589 nm is 0 nm or more and 10 nm or less. The optical film of the present invention has a thickness direction retardation Rth of -10 nm to 10 nm for light having a wavelength of 589 nm. The optical film of the present invention is a biaxially stretched film.

  Here, the refractive index in the direction of the slow axis in the plane of the optical film is nx, the refractive index in the direction of the fast axis in the plane is ny, the refractive index in the thickness direction of the optical film is nz, When the thickness of the optical film is d, the in-plane retardation Re and the thickness direction retardation Rth are represented by the formula Re = (nx−ny) × d and the formula Rth = {(nx + ny) / 2−, respectively. nz} × d.

  The structural unit having an action of imparting positive intrinsic birefringence to a polymer refers to a structural unit in which the homopolymer exhibits positive intrinsic birefringence when the homopolymer of the structural unit is formed. The structural unit having an effect of giving negative intrinsic birefringence to a polymer refers to a structural unit in which the homopolymer exhibits negative intrinsic birefringence when the homopolymer of the structural unit is formed.

  The positive or negative of the intrinsic birefringence of the polymer is the direction in which the molecular chains in the layer of the layer in which the molecular chains of the polymer are uniaxially oriented (for example, a film) in the layer perpendicular to the main surface of the layer. This can be determined based on a value “n1-n2” obtained by subtracting the refractive index n2 of the layer for the vibration component perpendicular to the orientation axis from the refractive index n1 of the layer for the vibration component parallel to the (orientation axis). The intrinsic birefringence value can be determined by calculation based on the molecular structure of each polymer.

  The polarizer protective film of the present invention is constituted by the optical film of the present invention.

  The polarizing plate of this invention is equipped with the polarizer protective film of the said invention, and a polarizer.

  The image display device of the present invention includes the optical film of the present invention.

  In the present invention, an N-substituted maleimide unit (a) having an action of imparting positive intrinsic birefringence to the polymer, and a (meth) acrylate unit (b) having an action of imparting negative intrinsic birefringence to the polymer. The (meth) acrylic polymer (c) having the above as a structural unit is used for the optical film. Thereby, although it is a biaxially stretched film, the retardation which shows is small and the optical film which has high heat resistance is implement | achieved.

It is sectional drawing which shows an example of the optical film of this invention typically. It is sectional drawing which shows typically an example of the polarizer protective film of this invention. It is sectional drawing which shows typically an example of the polarizing plate of this invention. It is sectional drawing which shows typically an example of the image display apparatus of this invention.

  Hereinafter, preferred embodiments of the present invention will be described. The present invention is not limited to the following embodiments.

[(Meth) acrylic polymer (c)]
The (meth) acrylic polymer (c) used in the optical film of the present invention has N-substituted maleimide units (a) and (meth) acrylic acid ester units (b) as structural units. The N-substituted maleimide unit (a) has a molecular structure that gives positive intrinsic birefringence to the (meth) acrylic polymer (c) having the unit.

  The N-substituted maleimide unit (a) is preferably an N-alkyl substituted maleimide having an effect of imparting positive intrinsic birefringence to the polymer. The alkyl group which is a substituent is a C1-C20 alkyl group, for example, and a C1-C20 aliphatic alkyl group is preferable. The alkyl group can be linear, branched and cyclic. N-substituted maleimide units (a) are, for example, N-methylmaleimide, N-ethylmaleimide, N-isopropylmaleimide, Nn-butylmaleimide, N-isobutylmaleimide, Nt-butylmaleimide, Nn- It is a structural unit derived from each monomer of hexylmaleimide, N-2-ethylhexylmaleimide, N-dodecylmaleimide, N-laurylmaleimide, N-cyclohexylmaleimide, and N-benzylmaleimide. The (meth) acrylic polymer (c) may contain one or more of these N-substituted maleimide units. The N-substituted maleimide unit (a) is particularly preferably an N-cyclohexylmaleimide unit because the thermal stability and optical properties of the optical film are enhanced.

In addition, N-substituted maleimide units (for example, N-phenylmaleimide units, N-chlorophenylmaleimide units) having an aromatic group Ar ¹ as a substituent as disclosed in Patent Document 2 (Japanese Patent Laid-Open No. 2007-31537). Unit, N-methylphenylmaleimide unit, N-methoxyphenylmaleimide unit, N-naphthylmaleimide unit) usually has a function of giving negative intrinsic birefringence to the polymer.

  The (meth) acrylic acid ester unit (b) has a molecular structure that gives negative intrinsic birefringence to the (meth) acrylic polymer (c) having the unit.

  In the (meth) acrylic polymer (c), the N-substituted maleimide unit (a) has a function of giving positive intrinsic birefringence, and the (meth) acrylate unit (b) gives a negative intrinsic birefringence. Has an effect. For this reason, when the (meth) acrylic polymer (c), which is a copolymer having both structural units, is stretched, the birefringences generated by both structural units cancel each other. Thereby, although it is a biaxially stretched film, both the in-plane retardation Re and the thickness direction retardation Rth are small, and an optical film is obtained.

  The (meth) acrylic acid ester unit (b) is not limited as long as it has an effect of giving negative intrinsic birefringence to the polymer. The (meth) acrylic acid ester unit (b) is, for example, methyl (meth) acrylate, ethyl (meth) acrylate, n-propyl (meth) acrylate, isopropyl (meth) acrylate, (meth) acrylic acid n. -Butyl, t-butyl (meth) acrylate, n-hexyl (meth) acrylate, 2-ethylhexyl (meth) acrylate, chloromethyl (meth) acrylate, 2-chloroethyl (meth) acrylate, (meth) 2-hydroxyethyl acrylate, 3-hydroxypropyl (meth) acrylate, 2,3,4,5,6-pentahydroxyhexyl (meth) acrylate, 2,3,4,5-tetra (meth) acrylate It is a structural unit derived from each monomer of hydroxypentyl. The (meth) acrylic polymer (c) may contain one or more of these (meth) acrylic acid ester units. The (meth) acrylic acid ester unit (b) is particularly preferably a methyl methacrylate (MMA) unit because the thermal stability and optical properties of the optical film are enhanced. In addition, the optical film which consists of PMMA which is a homopolymer of a MMA unit shows the tendency for the phase difference Rth of a thickness direction to become large especially by biaxial stretching.

  The content of the N-substituted maleimide unit (a) in the (meth) acrylic polymer (c) is preferably 5% by mass to 30% by mass, more preferably 5% by mass to 25% by mass, More preferably, they are 8 mass% or more and 22 mass% or less, Most preferably, they are 10 mass% or more and 22 mass% or less. The content of the (meth) acrylic acid ester unit (b) in the (meth) acrylic polymer (c) is preferably 70% by mass to 95% by mass, and more preferably 75% by mass to 95% by mass. More preferably, it is 78 mass% or more and 92 mass% or less, Most preferably, it is 78 mass% or more and 90 mass% or less. When the content of the N-substituted maleimide unit (a) and the (meth) acrylic acid ester unit (b) in the (meth) acrylic polymer (c) is within these ranges, the position shown while being a biaxially stretched film An optical film having a smaller phase difference and higher heat resistance can be obtained. In addition to this, the in-plane retardation Re and the thickness direction retardation Rth are suppressed over the entire visible light region (approximately 380 nm to 750 nm) while being a biaxially stretched film.

  When the (meth) acrylic polymer (c) has the N-substituted maleimide unit (a) as a constituent unit, the glass transition temperature (Tg) of the polymer (c) is improved. Thereby, the heat resistance of the optical film containing the said polymer (c) improves. The Tg of the (meth) acrylic polymer (c) is, for example, 110 ° C. or higher. Depending on the type and content of the N-substituted maleimide unit (a) and (meth) acrylic acid ester unit (b), the Tg of the (meth) acrylic polymer (c) is 115 ° C. or higher, 120 ° C. or higher, 125 ° C or higher. Since the Tg of the (meth) acrylic polymer (c) is so high, the optical film of the present invention is an image display in which heating elements such as a power source, a light source, and a semiconductor circuit are housed in a narrow space with a high density. Suitable for use in devices. The upper limit of Tg of the (meth) acrylic polymer (c) is not particularly limited, but is preferably 200 ° C. or lower because the polymer and the resin composition containing the polymer can be easily molded.

  In addition, Tg of (meth) acrylic polymer (c) improves, so that there are many content rates of N-substituted maleimide unit (a). However, when the content exceeds 30% by mass, the amount of monomer remaining in the (meth) acrylic polymer (c) tends to increase. When the amount of the remaining monomer is large, the workability at the time of molding the resin composition containing the (meth) acrylic polymer (c) is lowered, and the productivity of the optical film may be lowered.

  The N-substituted maleimide unit (a) is a ring structure located in the main chain of the (meth) acrylic polymer (c). As the ring structure introduced into the main chain of the (meth) acrylic polymer in order to adjust Tg and / or optical properties, a maleic anhydride structure and a glutaric anhydride structure are also known. The (meth) acrylic polymer (c) having an N-substituted maleimide unit (a) is less susceptible to thermal decomposition than the (meth) acrylic polymer having these other ring structures in the main chain. Due to this feature, for example, when a (meth) acrylic polymer (c) and a resin composition containing the polymer (c) are melt filtered (for example, melt filtration using a polymer filter) and / or melt-molded, ) Foaming due to thermal decomposition of the acrylic polymer (c) is suppressed. Foaming is an optical defect in the optical film. For this reason, the optical film of the present invention containing the (meth) acrylic polymer (c) in which foaming due to thermal decomposition is suppressed while having a ring structure in the main chain is suitable for optical applications including image display devices. Is suitable for use.

  The weight average molecular weight of the (meth) acrylic polymer (c) is preferably 2,000 to 1,000,000, more preferably 10,000 to 500,000, still more preferably 50,000 to 300. , 000.

  The (meth) acrylic polymer (c) can have a structural unit (d) other than the N-substituted maleimide unit (a) and the (meth) acrylic acid ester unit (b) as long as the effects of the present invention are obtained. . The content of the structural unit (d) in the (meth) acrylic polymer (c) is preferably 0 to 10% by mass, more preferably 0 to 5% by mass, and further preferably 0 to 2% by mass. Yes, particularly preferably 0 to 1% by mass.

  The structural unit (d) in the (meth) acrylic polymer (c) is “monomer that becomes N-substituted maleimide unit (a) by polymerization” and “(meth) acrylic acid ester unit (b) by polymerization”. “Monomer” is a structural unit derived from a monomer that can be polymerized with both monomers. The structural unit (d) is, for example, acrylic acid, methacrylic acid, crotonic acid, maleic anhydride, 2- (hydroxymethyl) acrylic acid, 2- (hydroxyethyl) acrylic acid, cyclohexyl (meth) acrylate, (meth). Benzyl acrylate, dicyclopentanyl (meth) acrylate, dicyclopentanyloxyethyl (meth) acrylate, styrene, vinyl toluene, α-methyl styrene, α-hydroxymethyl styrene, α-hydroxyethyl styrene, acrylonitrile, Each of methacrylonitrile, methallyl alcohol, allyl alcohol, ethylene, propylene, 4-methyl-1-pentene, vinyl acetate, 2-hydroxymethyl-1-butene, methyl vinyl ketone, N-vinyl pyrrolidone, N-vinyl carbazole Constituent units derived from monomers It is. As long as the effect of the present invention is obtained, the (meth) acrylic polymer (c) may have two or more structural units (d).

  The structural unit (d) can be added to the polymer (c), for example, in order to prevent the Tg of the (meth) acrylic polymer (c) from becoming excessively high.

[Optical film]
FIG. 1 shows an example of the optical film of the present invention. The optical film 1 shown in FIG. 1 includes a (meth) acrylic polymer (c) having N-substituted maleimide units (a) and (meth) acrylic acid ester units (b) as constituent units. Typically, the optical film 1 consists of a resin composition containing a (meth) acrylic polymer (c).

  The optical film 1 exhibits an in-plane retardation Re of 0 nm to 10 nm with respect to light having a wavelength of 589 nm. The optical film 1 exhibits a thickness direction retardation Rth of −10 nm to 10 nm with respect to light having a wavelength of 589 nm. The optical film 1 is suitable for use as a polarizer protective film because both the in-plane retardation Re and the thickness direction retardation Rth have a small retardation. In particular, the small phase difference Rth in the thickness direction means that sufficient viewing angle characteristics can be secured in a large-screen image display device.

  The optical film 1 is a biaxially stretched film. By biaxial stretching, the optical film 1 exhibits sufficient mechanical properties (for example, strength and flexibility) as an optical film, particularly as a polarizer protective film. In a biaxially stretched film, even if the in-plane retardation Re is suppressed, the retardation Rth in the thickness direction tends to increase. However, although the optical film 1 is a biaxially stretched film, the thickness direction retardation Rth is also small.

  Depending on the composition of the material constituting the optical film 1, the in-plane retardation Re and / or the thickness direction position can be obtained by biaxial stretching while exhibiting sufficient mechanical properties as an optical film, particularly as a polarizer protective film. The phase difference Rth is further reduced. In the optical film 1, the in-plane retardation Re for light having a wavelength of 589 nm is preferably 0 nm or more and less than 10 nm, more preferably 0 nm or more and 5 nm or less, further preferably 0 nm or more and 3 nm or less, and particularly preferably 0 nm. It is 2 nm or less. In the optical film 1, the thickness direction retardation Rth with respect to light having a wavelength of 589 nm is preferably −5 nm to 5 nm, more preferably −3 nm to 3 nm, and further preferably −2 nm to 2 nm. . The optical film 1 exhibiting such a small in-plane retardation Re and / or thickness direction retardation Rth is particularly suitable for use in an image display device such as an LCD. Good viewing angle characteristics and contrast characteristics can be obtained.

  The optical film 1 has an in-plane retardation Re and a thickness direction retardation Rth over the entire visible light range while exhibiting sufficient mechanical properties as an optical film, particularly as a polarizer protective film, by biaxial stretching. small. For example, the in-plane retardation Re for light having a wavelength of 400 nm and light having a wavelength of 750 nm is 0 nm or more and 10 nm or less. Depending on the composition of the material constituting the optical film 1, the in-plane retardation Re for light having a wavelength of 400 nm and light having a wavelength of 750 nm is 0 nm to 5 nm, 0 nm to 3 nm, and further 0 nm to 2 nm. For example, the thickness direction retardation Rth for light having a wavelength of 400 nm and light having a wavelength of 750 nm is not less than −10 nm and not more than 10 nm. Depending on the composition of the material constituting the optical film 1, the thickness direction retardation Rth for light having a wavelength of 400 nm and light having a wavelength of 750 nm is -5 nm to 5 nm, -3 nm to 3 nm, and further −2 nm to 2 nm. It becomes.

  The optical film 1 has an in-plane retardation Re of 0 nm or more and 5 nm or less for light having a wavelength of 400 nm and a wavelength of 750 nm, and a thickness direction retardation Rth of −10 nm or more and 10 nm or less for light of a wavelength of 400 nm or wavelength 750 nm. Is preferred.

In the optical film 1, the birefringence in the thickness direction of the film, represented by Rth / d, is preferably −2 × 10 ⁻⁴ or more and 2 × 10 ⁻⁴ or less, more preferably −1 × 10 ⁻⁴ It is 1 × 10 ⁻⁴ or less, more preferably −0.5 × 10 ⁻⁴ or more and 0.5 × 10 ⁻⁴ or less. In these ranges, since the birefringence in the thickness direction of the optical film 1 is small, the degree of freedom in setting the thickness of the film increases. More specifically, it is possible to set the thickness sufficiently considering the strength and flexibility without excessively reducing the thickness of the optical film 1. That is, setting these ranges is advantageous for the strength and flexibility of the optical film 1. Note that Rth is a retardation in the thickness direction of the optical film (unit: nm) with respect to light having a wavelength of 589 nm, and d is a thickness (unit: nm) of the optical film.

  Since the optical film 1 contains the (meth) acrylic polymer (c) which has an N-substituted maleimide unit (a) as a structural unit, it is excellent in heat resistance. The Tg of the optical film 1 is, for example, 110 ° C. or higher. Depending on the composition of the (meth) acrylic polymer (c) and the content of the polymer (c) in the optical film 1, it is 115 ° C. or higher, 120 ° C. or higher, and further 125 ° C. or higher. The optical film 1 having such a high Tg is suitable for use in an image display device in which heating elements such as a power source, a light source, and a semiconductor circuit are housed in a narrow space at a high density. The optical film 1 having a high Tg also improves the degree of freedom in designing the image display device including the film 1 such that the arrangement in the vicinity of a heat generating part such as a light source in the image display device is easy. Although the upper limit of Tg of the optical film 1 is not specifically limited, 200 degreeC or less is preferable from a viewpoint of the moldability of the said film 1, and 180 degreeC or less is more preferable.

  The content of the (meth) acrylic polymer (c) in the optical film 1 is preferably 60% by mass or more and 100% by mass or less, more preferably 70% by mass or more and 100% by mass or less, and further preferably 80% by mass. % To 100% by mass, particularly preferably 90% to 100% by mass. The optical film 1 can consist of a (meth) acrylic polymer (c).

  The optical film 1 may contain a material other than the (meth) acrylic polymer (c) in a resin composition constituting the optical film 1 in a content of less than 40% by mass, preferably less than 10% by mass.

  The material is, for example, a thermoplastic resin having compatibility with the polymer (c) other than the (meth) acrylic polymer (c). Examples of the thermoplastic resin include olefin polymers such as polyethylene, polypropylene, ethylene-propylene copolymer, and poly (4-methyl-1-pentene); halogen-containing polymers such as vinyl chloride and chlorinated vinyl resins; polystyrene, styrene -Styrene polymers such as methyl methacrylate copolymer, styrene-acrylonitrile copolymer, acrylonitrile-butadiene-styrene block copolymer; (meth) acrylic polymers such as polymethyl methacrylate; polyethylene terephthalate, polybutylene terephthalate, polyethylene Polyester such as phthalate; cellulose ester such as triacetyl cellulose; polyamide such as nylon 6, nylon 66, nylon 610; polyacetal: polycarbonate; Eniren'okishido; polyphenylene sulfide polyether ether ketone; polyether nitrile; polysulfone; polyether sulfone; a polyamide-imide; polyoxyethylene Penji Ren.

  The material is, for example, an additive. Additives include, for example, UV absorbers such as benzotriazoles, benzophenones, salicates, benzoates, and triazines; antioxidants such as phenols, phosphates, and thioethers; retardation increasing agents, retardation reduction Retardation adjusters such as agents; Stabilizers such as retardation stabilizers, light stabilizers, weathering stabilizers, heat stabilizers; reinforcing materials such as glass fibers and carbon fibers; near infrared absorbers; tris (dibromopropyl) phosphate Flame retardants such as triaryl phosphate and antimony oxide; antistatic agents represented by anionic, cationic and nonionic surfactants; colorants such as inorganic pigments, organic pigments and dyes; organic fillers and inorganic fillers; Resin modifiers; plasticizers; lubricants; flame retardants; rubbery polymers such as ASA and ABS. The amount of these additives added to the optical film 1 is, for example, 0% by mass or more and 5% by mass or less, preferably 0% by mass or more and 2% by mass or less, more preferably 0% by mass or more and 0.5% by mass or less. It is as follows. When the additive amount is excessively large, bleeding out and / or silver streaks are likely to occur when the optical film 1 is formed.

  The thickness of the optical film 1 is not limited. The thickness of the optical film 1 is, for example, 5 μm or more and 250 μm or less, preferably 10 μm or more and 150 μm or less, and more preferably 20 μm or more and 80 μm or less. When the thickness is smaller than 5 μm, the strength as an optical film may be insufficient. If the thickness is greater than 250 μm, the birefringence of the film may become excessively large.

  The manufacturing method of the optical film 1 is not limited. The optical film 1 can be manufactured by applying a known method. For example, the optical film 1 is manufactured by shape | molding the resin composition containing a (meth) acrylic polymer (c), forming a film, and biaxially stretching the obtained film.

  The method for forming a film by molding the resin composition is not particularly limited, and examples thereof include cast molding, melt extrusion molding, and press molding.

  As described above, the (meth) acrylic polymer (c) is hardly thermally decomposed. For this reason, the optical film 1 can be suitably manufactured by melt extrusion molding.

  Melt extrusion molding is implemented with respect to the resin composition containing a (meth) acrylic polymer (c), for example. The resin composition is prepared by, for example, pre-blending the (meth) acrylic polymer (c) and other components in the resin composition with a mixer such as an omni mixer, and then extruding and kneading the resulting mixture from a kneader. Can be formed. As the kneader, a known kneader, for example, an extruder such as a single screw extruder or a twin screw extruder, and a pressure kneader can be applied.

  Melt extrusion molding follows, for example, a T-die method and an inflation method. The temperature of the melt extrusion molding (molding temperature) is preferably 200 ° C. or higher and 350 ° C. or lower, more preferably 250 ° C. or higher and 300 ° C. or lower, further preferably 255 ° C. or higher and 300 ° C. or lower, particularly preferably 260 ° C. or higher and 300 ° C. or lower. is there.

  According to the T-die method, a film wound around a roll can be obtained by winding up a film extruded from an extruder having a T-die attached to the tip. At this time, stretching (uniaxial stretching) can be applied in the extrusion direction of the film by controlling the winding temperature and speed.

  When an extruder is used for melt extrusion molding, the type of the extruder is not particularly limited, and may be uniaxial, biaxial, and multiaxial. The L / D value of the extruder (L is the length of the cylinder of the extruder, D is the inner diameter of the cylinder), and the resin composition containing the (meth) acrylic polymer (c) is sufficiently plasticized to be in a good kneaded state In order to obtain the above, it is preferably 10 or more and 100 or less, more preferably 15 or more and 80 or less, and further preferably 20 or more and 60 or less. When the L / D value is less than 10, the resin composition cannot be sufficiently plasticized and a good kneaded state may not be obtained. When the L / D value exceeds 100, excessive heat generation is applied to the resin composition, so that the components contained in the resin composition are easily decomposed.

  In this case, the set temperature of the cylinder is preferably 200 ° C. or higher and 350 ° C. or lower, more preferably 250 ° C. or higher and 320 ° C. or lower. When setting temperature is less than 200 degreeC, the melt viscosity of the resin composition containing a (meth) acrylic polymer (c) becomes high too much, and the productivity of a film falls. When setting temperature exceeds 350 degreeC, the component contained in a resin composition may thermally decompose.

  When an extruder is used for melt extrusion molding, the shape of the extruder is not particularly limited. It is preferred that the extruder has one or more open vents. By using such an extruder, cracked gas can be sucked from the open vent portion. Thereby, the quantity of the volatile component which remains in the obtained film is reduced. In order to suck the decomposition gas from the open vent portion, for example, the open vent portion is in a reduced pressure state. In this case, the degree of decompression is preferably 1.3 hPa or more and 931 hPa or less, more preferably 13.3 hPa or more and 798 hPa or less in terms of the pressure (absolute pressure) of the open vent part. When the pressure in the open vent portion is higher than 931 hPa, monomers generated by decomposition of the volatile component and / or the component contained in the resin composition tend to remain in the obtained film. On the other hand, it is industrially difficult to keep the pressure of the open vent part lower than 1.3 hPa.

  At the time of melt extrusion molding, it is preferable to melt filter the resin composition containing the (meth) acrylic polymer (c) in a molten state using a polymer filter. Foreign matter present in the resin composition is removed by melt filtration. For this reason, the amount of optical defects and appearance defects in the finally obtained optical film is reduced. As described above, the (meth) acrylic polymer (c) is difficult to be thermally decomposed, and therefore foaming is unlikely to occur during melt filtration. However, melt filtration at excessively high temperatures causes defects such as perforations, flow patterns and flow streaks in the resulting film. These defects are particularly likely to occur during continuous film formation. Considering these, the temperature of the melt extrusion molding is, for example, 200 ° C. or more and 350 ° C. or less in order to shorten the residence time of the composition in the polymer filter by lowering the melting temperature of the resin composition. Is 250 ° C. or higher and 320 ° C. or lower.

  The configuration of the polymer filter is not particularly limited. A polymer filter in which a large number of leaf disk filters are arranged in a housing can be suitably used. As the filter medium of the leaf disk type filter, any of a type in which a metal fiber nonwoven fabric is sintered, a type in which metal powder is sintered, a type in which several metal meshes are laminated, or a hybrid type in which these are combined can be used. A type in which a metal fiber nonwoven fabric is sintered is most preferable.

  The filtration accuracy of the polymer filter is not particularly limited. The filtration accuracy is usually 15 μm or less, preferably 10 μm or less, more preferably 5 μm or less. When the filtration accuracy is 1 μm or less, the resin composition in the polymer filter has a long residence time, so that the thermal deterioration of the composition increases. Moreover, the productivity of the film decreases. When the filtration accuracy exceeds 15 μm, the removal of foreign matters contained in the resin composition tends to be insufficient.

  The shape of the polymer filter is not particularly limited. The polymer filter is, for example, an internal flow type having a plurality of resin flow ports and a resin flow path in the center pole; the cross section is in contact with the inner peripheral surface of the leaf disk filter at a plurality of vertices or faces, An external flow type having a resin flow path on the outer surface. The use of an external flow type is preferred because there are few resin stays.

  The residence time of the resin in the polymer filter is preferably 20 minutes or less, more preferably 10 minutes or less, and even more preferably 5 minutes or less. In the melt filtration, the inlet pressure of the polymer filter and the outlet pressure of the filter are, for example, 3 MPa to 15 MPa and 0.3 MPa to 10 MPa, respectively. The pressure loss in melt filtration (pressure difference between the inlet pressure and the outlet pressure of the polymer filter) is preferably 1 MPa or more and 15 MPa or less. When the pressure loss is 1 MPa or less, the flow path through which the resin composition passes through the polymer filter tends to be biased. The unevenness of the flow path is a cause of deterioration in the quality of the obtained film. When the pressure loss exceeds 15 MPa, the polymer filter is easily damaged.

  Melt filtration using a polymer filter can be performed at any timing, such as during the formation of a resin composition, other than during melt extrusion molding.

  When melt filtering the resin composition, it is preferable to stabilize the pressure of the resin composition in the polymer filter by installing a gear pump between the extruder and the polymer filter.

  The film obtained by various molding methods is then biaxially stretched to form the optical film 1. When uniaxial stretching is already applied when the film is formed, a biaxially stretched film is obtained by performing the remaining uniaxial stretching.

  As long as the optical film 1 is obtained, the method of biaxial stretching is not limited. Biaxial stretching may be, for example, two-stage stretching of longitudinal stretching and lateral stretching. The biaxial stretching may be, for example, three-stage stretching (or three-stage or more multi-stage stretching) such as longitudinal stretching—lateral stretching—longitudinal stretching or transverse stretching—longitudinal stretching—transverse stretching. The optical film 1 is a biaxially stretched film, and therefore has high strength and excellent film thickness uniformity. An unstretched film has a small retardation, but does not have sufficient strength for use as an optical film. A uniaxially stretched film tends to cause anisotropy in optical properties and strength, and exhibits a large retardation.

  The stretching temperature is not limited. The stretching temperature is preferably a temperature in the vicinity of Tg of the resin composition containing the (meth) acrylic polymer (c). The stretching temperature is, for example, Tg-20 ° C or higher and Tg + 50 ° C or lower, preferably Tg-10 ° C or higher and Tg + 30 ° C or lower. When the stretching temperature is Tg-20 ° C. or lower, the film is easily broken during stretching. When the stretching temperature is Tg + 50 ° C. or higher, the effect of stretching cannot be obtained sufficiently. The stretching speed is not particularly limited, and is, for example, 10% / min or more and 20000% / min or less, and preferably 100% / min or more and 10000% / min or less. When the stretching speed is less than 10% / min, the time until the stretching is completed becomes long, so that the production cost of the optical film increases. When the stretching speed exceeds 20000% / min, the film is easily broken during stretching.

  The draw ratio in terms of area ratio is preferably 1.2 times or more and 25 times or less, more preferably 1.5 times or more and 15 times or less, and further preferably 2 times or more and 10 times or less. When the draw ratio is less than 1.2, sufficient mechanical properties (for example, strength and flexibility) cannot be obtained. When the draw ratio exceeds 25 times, there is no merit by further increasing the draw ratio, and the film is likely to break during stretching.

  In order to stabilize the optical properties and mechanical properties of the optical film, heat treatment (annealing) may be performed as necessary after stretching.

  Various functional coating layers can be formed on the surface of the optical film of the present invention as necessary. Functional coating layers include, for example, antistatic layers, adhesive layers, adhesive layers, easy adhesion layers, antiglare (non-glare) layers, antifouling layers such as photocatalyst layers, antireflection layers, hard coat layers, and UV shielding layers. A layer, a heat ray shielding layer, an electromagnetic wave shielding layer, and a gas barrier layer.

  The use of the optical film of the present invention is not particularly limited. The optical film of the present invention is suitable for the following uses based on a small retardation, high transparency, and high heat resistance. The application is, for example, an optical protective film, specifically, a protective film for substrates of various optical disks (VD, CD, DVD, MD, LD, etc.), and a polarization used in a polarizing plate included in an image display device such as an LCD. It is a child protection film. Viewing angle compensation film, light diffusion film, reflection film, antireflection film, antiglare film, brightness enhancement film, conductive film for touch panel, retardation film (however, in-plane retardation Re for light having a wavelength of 589 nm is 10 nm or less, and The optical film of the present invention can be used as an optical film having a thickness direction retardation Rth of -10 nm to 10 nm. The optical film of the present invention is particularly suitable for use as a polarizer protective film.

[Polarizer protective film and polarizing plate]
In FIG. 2, an example of the polarizer protective film of this invention is shown. The polarizer protective film 2 shown in FIG. 2 is comprised by the optical film of this invention. That is, the polarizer protective film 2 includes a (meth) acrylic polymer (c) having N-substituted maleimide units (a) and (meth) acrylic acid ester units (b) as constituent units. The N-substituted maleimide unit (a) is a structural unit having an action of imparting positive intrinsic birefringence to the (meth) acrylic polymer (c). The (meth) acrylic acid ester unit (b) is a structural unit having an action of giving negative intrinsic birefringence to the (meth) acrylic polymer (c). The polarizer protective film 2 exhibits an in-plane retardation Re of 0 nm to 10 nm with respect to light having a wavelength of 589 nm. The polarizer protective film 2 exhibits a thickness direction retardation Rth of −10 nm to 10 nm with respect to light having a wavelength of 589 nm. The polarizer protective film 2 is a biaxially stretched film.

  FIG. 3 shows an example of the polarizing plate of the present invention. A polarizing plate 3 shown in FIG. 3 includes the polarizer protective film 2 of the present invention and the polarizer 4. The polarizer 4 is sandwiched between a pair of polarizer protective films 2. The polarizer 4 and the polarizer protective film 2 are in contact with each other.

  The polarizer 4 is not limited, and any appropriate polarizer can be adopted depending on the function required for the polarizing plate 3. The polarizer 4 is made of, for example, a hydrophilic polymer film such as a polyvinyl alcohol (PVA) film, a partially formalized PVA film, or a partially saponified film of ethylene-vinyl acetate copolymer (EVA). A film uniaxially stretched by adsorbing a dichroic substance such as a chromatic dye; a polyene-based oriented film using a PVA dehydrated product or a polyvinyl chloride dehydrochlorinated product. Among these, a film obtained by adsorbing a dichroic substance to a PVA film and uniaxially stretching is preferable as the polarizer 4. This polarizer exhibits a high polarization dichroic ratio. The thickness of the polarizer 4 is not limited, and is generally about 1 to 80 μm.

  The polarizing plate 3 is typically manufactured by laminating the polarizer protective film 2 and the polarizer 4 via an adhesive layer. Specifically, for example, an adhesive composition that becomes an adhesive layer after drying is applied to one surface selected from the polarizer 4 or the polarizer protective film 2, and then both are bonded and dried. Examples of the method for applying the adhesive composition include a roll method, a spray method, and a dipping method. When the adhesive composition contains a metal compound colloid, the adhesive composition is applied so that the thickness of the adhesive layer after drying is larger than the average particle diameter of the metal compound colloid particles. The drying temperature is typically 5 ° C. or higher and 150 ° C. or lower, preferably 30 ° C. or higher and 120 ° C. or lower. The drying time is typically 120 seconds or longer, preferably 300 seconds or longer.

  The polarizing plate of the present invention may be provided with at least one polarizer protective film 2.

  The polarizer protective film and the polarizing plate of the present invention are suitable for use in an image display device. The image display device is, for example, an electroluminescence (EL) display panel, a plasma display panel (PDP), a field emission display (FED), or an LCD. The LCD includes a liquid crystal cell and a polarizing plate disposed on at least one main surface of the liquid crystal cell. The polarizing plate of the present invention is suitable for the polarizing plate.

[Image display device]
The image display device of the present invention includes the optical film of the present invention. The optical film is, for example, a polarizer protective film. The image display device is, for example, an EL display panel, PDP, FED, or LCD.

  The configuration of the image display device including the optical film of the present invention (image display device of the present invention) is not particularly limited, and members such as a power source, a backlight unit, and an operation unit can be appropriately provided as necessary.

  FIG. 4 shows an example of the structure of the image display unit in the image display apparatus of the present invention. The image display unit 11 shown in FIG. 4 is an image display unit of an LCD, and includes a liquid crystal cell 5, a pair of polarizing plates 3a and 3b arranged so as to sandwich the liquid crystal cell 5, and the liquid crystal cell 5 and the polarizing plate 3a. , 3b, and a backlight 8 arranged on one surface of the laminate. Each polarizing plate 3a, 3b includes polarizers 4a, 4b and a pair of polarizer protective films 2a, 2b, 2c, 2d arranged so as to sandwich the polarizer. The liquid crystal cell 5 has a known structure, and includes, for example, a liquid crystal layer, a glass substrate, a transparent electrode, an alignment film, and the like. The backlight 8 has a known structure, and includes, for example, a light source, a reflection sheet, a light guide plate, a diffusion plate, a diffusion sheet, a prism sheet, and a brightness enhancement film.

  In the image display unit 11, for example, at least one selected from four polarizer protective films 2a to 2d is the optical film of the present invention. Any polarizer protective film may be the optical film of the present invention. The image display unit 11 may further include an arbitrary optical film such as a retardation film or an optical compensation film and an optical member as necessary. The optical film can be the optical film of the present invention. The optical member may include the optical film of the present invention.

  The image display device of the present invention can include the polarizer protective film of the present invention and / or the polarizing plate of the present invention.

  The following examples further illustrate the present invention. The present invention is not limited to the following examples.

  Initially, the evaluation method of the polymer and optical film which were produced in the present Example is shown.

[Glass transition temperature (Tg)]
The Tg of the polymer was determined by the starting point method in accordance with JIS K7121 regulations. Specifically, a differential scanning calorimeter (manufactured by Rigaku, DSC-8230) is used, and a sample of about 10 mg is heated from normal temperature to 200 ° C. (temperature increase rate: 20 ° C./min) in a nitrogen gas atmosphere. The DSC curve was evaluated. Α-alumina was used as a reference.

[Weight average molecular weight]
The weight average molecular weight of the polymer was determined in terms of polystyrene using gel permeation chromatography (GPC). The apparatus and measurement conditions used for the measurement are as follows.
System: Tosoh GPC system HLC-8220
Measurement side column configuration ・ Guard column: Tosoh, TSKguardcolumn SuperHZ-L
・ Separation column: Tosoh, TSKgel SuperHZM-M 2 series connection Reference column configuration ・ Reference column: Tosoh, TSKgel SuperH-RC
Developing solvent: Chloroform (Wako Pure Chemical Industries, special grade)
Flow rate of developing solvent: 0.6 mL / min Standard sample: TSK standard polystyrene (manufactured by Tosoh, PS-oligomer kit)
Column temperature: 40 ° C

[Film thickness]
The thickness d (nm) of the film was measured using a Digimatic micrometer (manufactured by Mitutoyo).

[Refractive index anisotropy]
The in-plane retardation Re and the thickness direction retardation Rth of the film with respect to light having wavelengths of 400 nm, 589 nm, and 750 nm were measured using a retardation film / optical material inspection apparatus (Otsuka Electronics, RETS-100). did.

The thickness direction retardation value Rth is the average refractive index of the film measured with an Abbe refractometer, the thickness d of the film, and the in-plane retardation measured by tilting the film by 40 ° (Re (40 °)). ), And three-dimensional refractive indexes nx, ny and nz of the film, and then obtained from the following formula. nx, ny and nz are as described above.
Thickness direction retardation Rth (nm) = {(nx + ny) / 2−nz} × d (nm)

[Foaming test]
The foamability of the polymer was evaluated as follows. First, the dried polymer was filled into a cylinder of a melt indexer defined in JIS K7210. Next, after holding the cylinder filled with the polymer at 280 ° C. for 20 minutes, the polymer in the cylinder was extruded in a strand form from the tip of the cylinder. The number of bubbles with a major axis of 0.5 mm or more existing between the upper and lower strands of the strand thus obtained was measured visually, and this was evaluated by the number per 1 g of polymer. The evaluation criteria are as follows.
◎ (excellent): 1 or less ○ (good): 2 or more and 5 or less △ (possible): 6 or more and less than 10 × (impossible): 10 or more

(Production Example 1)
A reaction kettle equipped with a stirrer, a temperature sensor, a cooling pipe and a nitrogen introduction pipe was charged with 45 parts by mass of methyl methacrylate (MMA), 5 parts by mass of N-cyclohexylmaleimide (CHMI) and 50 parts by mass of toluene as a polymerization solvent, The temperature was raised to 105 ° C. while introducing nitrogen. When the reflux accompanying the temperature increase started, 0.04 parts by mass of t-amylperoxyisononanoate (manufactured by Atofina Yoshitomi, trade name: Luperox 570) was added as a polymerization initiator, and the above-mentioned t-amylperoxyisononoate was added. While 0.16 parts by mass of nanoate was added dropwise over 4 hours, solution polymerization was allowed to proceed under reflux at about 105 to 110 ° C., followed by further aging for 4 hours. Next, the obtained polymer solution was dried at 200 ° C. under reduced pressure for 1 hour to obtain a transparent solid of (meth) acrylic polymer (A-1) having CHMI units and MMA units as constituent units. It was. The weight average molecular weight of the polymer (A-1) was 230,000, and Tg was 126 ° C. The evaluation result of the foamability test for the polymer (A-1) was “◯ (good)”. The CHMI unit is a structural unit that gives positive intrinsic birefringence to the polymer. The MMA unit is a structural unit that gives negative intrinsic birefringence to the polymer. The content of CHMI units in the polymer (A-1) was 10% by mass, and the content of MMA units was 90% by mass.

(Production Example 2)
In the same manner as in Example 1, except that the amounts of MMA and CHMI were 40 parts by weight and 10 parts by weight, respectively, the aging time was 5 hours, and the drying temperature of the obtained polymerization solution was 220 ° C. A transparent solid of (meth) acrylic polymer (A-2) having CHMI units and MMA units as constituent units was obtained. The weight average molecular weight of the polymer (A-2) was 220,000, and Tg was 128 ° C. The evaluation result of the foamability test on the polymer (A-2) was “◎ (excellent)”. The content of CHMI units in the polymer (A-2) was 20% by mass, and the content of MMA units was 80% by mass.

Example 1
The polymer (A-1) produced in Production Example 1 was press molded at a molding temperature of 250 ° C. using a press molding machine to obtain a film (B-1) having a thickness of 152 μm. Next, the produced film (B-1) was subjected to a longitudinal direction using a biaxial stretching test apparatus (X-6S, manufactured by Toyo Seiki Seisakusho Co., Ltd.) at a stretching temperature of 146 ° C. and a stretching speed of 1000% / min. And in the order of the transverse direction, biaxial stretching was successively performed at a stretching ratio of 2 times and 1.5 times, respectively. The vertical direction means the so-called MD direction, and the horizontal direction means the so-called TD direction. After biaxial stretching, the film was quickly taken out from the test apparatus and cooled to obtain a biaxially stretched film (C-1) having a thickness of 55 μm. The obtained film (C-1) has a Tg of 126 ° C., an in-plane retardation Re for light of a wavelength of 589 nm of 1.2 nm, and a thickness direction retardation Rth of the light of −3.9 nm and a wavelength of 400 nm. The in-plane phase difference Re for the light is 1.3 nm, the thickness direction phase difference Rth for the light is −6.2 nm, the in-plane phase difference Re for the light of wavelength 750 nm is 2.0 nm, and the thickness direction position for the light is The phase difference Rth was -2.8 nm.

(Example 2)
The polymer (A-2) produced in Production Example 2 was press molded at a molding temperature of 255 ° C. using a press molding machine to obtain a film (B-2) having a thickness of 138 μm. Next, the produced film (B-2) was stretched in the machine direction using a biaxial stretching test apparatus (X-6S, manufactured by Toyo Seiki Seisakusho Co., Ltd.) at a stretching temperature of 148 ° C. and a stretching speed of 1000% / min. And in the order of the transverse direction, biaxial stretching was successively performed at a stretching ratio of 2 times and 1.5 times, respectively. After biaxial stretching, the film was quickly taken out from the test apparatus and cooled to obtain a biaxially stretched film (C-2) having a thickness of 43 μm. The obtained film (C-2) has a Tg of 128 ° C., an in-plane retardation Re for light of wavelength 589 nm of 0.4 nm, a thickness direction retardation Rth of the light of 0.8 nm, and light of wavelength 400 nm. The in-plane phase difference Re is 0.3 nm, the phase difference Rth in the thickness direction with respect to the light is 1.0 nm, the in-plane phase difference Re with respect to the light with a wavelength of 750 nm is 0.4 nm, and the phase difference Rth in the thickness direction with respect to the light. Was 0.8 nm.

(Comparative Example 1)
Polymethyl methacrylate (manufactured by Sumitomo Chemical Co., Ltd., trade name: Sumipex EX) was press molded at a molding temperature of 230 ° C. using a press molding machine to obtain a film (B-3) having a thickness of 146 μm. Next, the produced film (B-3) was machined in the longitudinal direction using a biaxial stretching test apparatus (X-6S, manufactured by Toyo Seiki Seisakusho, Ltd.) at a stretching temperature of 129 ° C. and a stretching speed of 1000% / min. And in the order of the transverse direction, biaxial stretching was successively performed at a stretching ratio of 2 times and 1.5 times, respectively. After biaxial stretching, the film was quickly taken out from the test apparatus and cooled to obtain a biaxially stretched film (C-3) having a thickness of 51 μm. The obtained film (C-3) has a Tg of 109 ° C., an in-plane retardation Re for the light of wavelength 589 nm of 6.1 nm, a thickness direction retardation Rth of the light of −11.1 nm, and a wavelength of 400 nm. The in-plane phase difference Re for the light is 6.2 nm, the phase difference Rth in the thickness direction for the light is −12.4 nm, the in-plane phase difference Re for the light with a wavelength of 750 nm is 5.7 nm, and the thickness direction relative to the light is The phase difference Rth was −10.8 nm.

  The evaluation result of the foamability test on the polymethyl methacrylate used in Comparative Example 1 was “x (impossible)”.

  The evaluation results of Examples and Comparative Examples are summarized in Table 1 below. Rth / d is a value for light with a wavelength of 589 nm.

  As shown in Table 1, in Examples 1 and 2, in particular, Example 2, both the in-plane retardation Re and the thickness direction retardation Rth of the obtained biaxially stretched film were small. . In addition, in Examples 1 and 2, particularly Example 2, it was confirmed that the in-plane phase difference Re and the thickness direction phase difference Rth were reduced over the entire visible light region. Furthermore, the polymers used in Examples 1 and 2, particularly the polymer used in Example 2, were hardly thermally decomposed and foaming during film formation was suppressed.

  The optical film of the present invention is suitable for use in various image display devices (liquid crystal display devices, organic EL display devices, PDPs, etc.).

DESCRIPTION OF SYMBOLS 1 Optical film 2, 2a, 2b, 2c, 2d Polarizer protective film 3, 3a, 3b Polarizing plate 4, 4a, 4b Polarizer 5 Liquid crystal cell 8 Backlight 11 Image display apparatus

Claims (7)

A (meth) acrylic polymer (c) having N-substituted maleimide units (a) and (meth) acrylic acid ester units (b) as constituent units,
The N-substituted maleimide unit (a) is a structural unit having an action of imparting positive intrinsic birefringence to the (meth) acrylic polymer (c), and includes a cyclohexylmaleimide unit,
The (meth) acrylic acid ester unit (b) is a structural unit having an action of giving negative intrinsic birefringence to the (meth) acrylic polymer (c),
The content of the N-substituted maleimide unit (a) in the (meth) acrylic polymer (c) is 8 % by mass or more and 30% by mass or less,
The content of the (meth) acrylic acid ester unit (b) in the (meth) acrylic polymer (c) is 70% by mass or more and 92 % by mass or less,
Wavelength 589nm in-plane retardation Re to light 0nm than 10nm or less, a retardation Rth in the thickness direction with respect to the light - is at 5 nm or more 5 nm or less,
The in-plane retardation Re for light having a wavelength of 400 nm and light having a wavelength of 750 nm is 5 nm or less,
The thickness direction retardation Rth for light having a wavelength of 400 nm and light having a wavelength of 750 nm is -10 nm or more and 10 nm or less,
The glass transition temperature is 110 ° C. or higher,
Biaxially oriented film Der is,
Excluding an optical film comprising a chain having a hydroxy group-containing part and an aromatic unit having an aromatic part, and a styrenic unit containing one or more styrenic derivatives ,
Optical film.
Here, the refractive index in the direction of the slow axis in the plane of the optical film is nx, the refractive index in the direction of the fast axis in the plane is ny, the refractive index in the thickness direction of the optical film is nz, When the thickness of the optical film is d, the in-plane retardation Re and the thickness direction retardation Rth are represented by the formula Re = (nx−ny) × d and the formula Rth = {(nx + ny) / 2−, respectively. nz} × d.   The optical film according to claim 1, wherein the N-substituted maleimide unit (a) is a cyclohexylmaleimide unit.   The optical film according to claim 1, wherein the (meth) acrylic acid ester unit (b) is a methyl methacrylate unit. 2. The optical film according to claim 1, wherein the birefringence in the thickness direction of the film represented by the formula Rth / d is −2 × 10 ⁻⁴ or more and 2 × 10 ⁻⁴ or less.   The polarizer protective film comprised with the optical film in any one of Claims 1-4.   A polarizing plate comprising the polarizer protective film according to claim 5 and a polarizer.   An image display apparatus provided with the optical film in any one of Claims 1-4.

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