WO2019203595A1 - Retardation film, polarizing plate comprising same, and liquid crystal display apparatus comprising same - Google Patents

Abstract

One embodiment of the present application relates to a retardation film, a polarizing plate comprising same, and a liquid crystal display apparatus comprising same, the retardation film comprising a composition or a cured product thereof, wherein the composition comprises an acrylate-based resin, a retardation controller having a glass transition temperature (Tg) of 130°C or higher, and a triazine-based birefringence controller, and 5-15 parts by weight of the triazine-based birefringence controller is included on the basis of 100 parts by weight of the acrylate-based resin.

Description

Retardation film, polarizing plate comprising the same and liquid crystal display comprising the same

This application claims the benefit of the date of application of Korean Patent Application No. 10-2018-0044907 filed to the Korean Intellectual Property Office on April 18, 2018 and Korean Patent Application No. 10-2019-0025264 filed on March 05, 2019. Claim, all of which are hereby incorporated by reference.

The present invention relates to a retardation film, a polarizing plate including the same, and a liquid crystal display including the same.

In recent years, the development of optical technology has been used to replace conventional CRTs, such as plasma display panels (PDPs), liquid crystal displays (LCDs), and organic light emitting diodes (OLEDs). Display devices using the scheme have been proposed and marketed. Recently, the characteristics required for such display apparatuses are becoming more advanced, and accordingly, the required characteristics for peripheral components such as optical films applied to the display apparatuses are also becoming more advanced. In particular, in recent years, display devices are becoming thinner, lighter, and larger in screen area, and wide viewing angles, high contrast, suppression of image color change according to viewing angle, and uniform display are particularly important problems.

The retardation film is an optical film used in a display device for the purpose of improving the viewing angle, display quality, and the like, and may be classified into one having a constant wavelength dispersion, a flat wavelength dispersion, and a reverse wavelength dispersion depending on the wavelength dispersion characteristics. A retardation film having a constant wavelength dispersion means a retardation film having a property of decreasing retardation value generated as the wavelength of incident light increases, and a retardation film having a flat wavelength dispersion has a similar degree regardless of the wavelength of incident light. It means a retardation film having a characteristic that generates a retardation value, the retardation film having a reverse wavelength dispersion means a retardation film having a characteristic that also increases as the wavelength of the incident light increases.

Most of the retardation films developed so far have a constant wavelength dispersion or a flat wavelength dispersion. In the case of a phase difference film having a constant wavelength dispersion or a flat wavelength dispersion, the phase retardation degree is changed when the light wavelength is changed. There is a problem that it is difficult to obtain a uniform color or luminous. On the other hand, in the case of having reverse wavelength dispersion, the phase delay value increases as the light wavelength increases, and thus, attention has been paid to the fact that a relatively uniform phase delay can be realized in a relatively wide light wavelength band.

However, since the wavelength dispersion is inherently characteristic according to the material of the retardation film, a retardation film having reverse wavelength dispersion in one sheet has to find a new raw material to manufacture, which is not easy in reality. Therefore, conventionally, two or more retardation films having different wavelength dispersions are laminated using an adhesive or an adhesive to produce a retardation film having reverse wavelength dispersion, or a resin having a positive retardation value and a resin having a negative retardation value are provided. Extruded to form a laminate, and stretched to produce a retardation film having a reverse wavelength dispersion is proposed.

However, in the case of the first method, if the optical axes of the two retardation films to be laminated are not disposed correctly, reverse wavelength dispersion does not appear, and thus manufacturing is very difficult. In the second method, the resin that forms each layer If the glass transition temperature is not similar, the stretching does not occur properly, there is a problem that the available resin is limited.

In addition, in the case of retardation film having improved wavelength dispersion by reverse wavelength dispersion or flat wavelength dispersion, the glass transition temperature is very low, resulting in a weak heat resistance.

Therefore, there is a demand for retardation film development that can realize reverse wavelength / flat wavelength dispersion that is easy to manufacture and excellent in heat resistance.

(Prior art document)

Korean public publication 2005-0101743

The present invention provides a retardation film, a polarizing plate including the same, and a liquid crystal display including the same.

An exemplary embodiment of the present application, the acrylate resin; Phase transition regulator having a glass transition temperature (Tg) of 130 ° C. or higher; And a retardation film comprising a composition comprising a triazine birefringence control agent or a cured product thereof, wherein the triazine birefringence control agent is included in an amount of 5 parts by weight or more and 15 parts by weight or less based on 100 parts by weight of the acrylate resin. To provide.

Another embodiment, the polarizer; And it provides a polarizing plate comprising at least one retardation film according to an embodiment of the present application.

Another embodiment, the liquid crystal cell; An upper polarizer provided in an upper layer of the liquid crystal cell; A lower polarizer provided in the lower layer of the liquid crystal cell; And a backlight unit provided under the lower polarizer, wherein at least one of the upper polarizer and the lower polarizer is a polarizer; And a phase difference film according to an exemplary embodiment of the present application disposed on one surface of the polarizer.

Retardation film according to the present invention is an acrylate resin; Phase transition regulator having a glass transition temperature (Tg) of 130 ° C. or higher; And a triazine-based birefringent modifier, the content of the specific conditions, to provide a retardation film excellent in heat resistance.

In addition, the retardation film according to the present invention, by using a specific amount of the triazine-based birefringent modifier, it is possible to implement the reverse wavelength / flat wavelength dispersion by changing the wavelength dispersion by using the refractive index difference with the acrylate resin, the present invention Since the retardation film of has a reverse wavelength dispersion property in which a phase retardation value becomes large as an optical wavelength becomes large, it can generate a relatively uniform degree of phase retardation in a wide optical band. As a result, when the retardation film of the present invention is applied to a polarizing plate or a display device, excellent color, luminous and optical properties can be realized.

1 is a view showing a laminated structure of a polarizing plate according to an exemplary embodiment of the present application.

2 is a view showing a laminated structure of a polarizing plate according to an exemplary embodiment of the present application.

3 is a view showing a liquid crystal display device according to an exemplary embodiment of the present application.

<Description of the code>

101: retardation film

102: polarizer

103: polarizer

104: polarizer protective film (retardation film)

105: adhesive layer (adhesive layer)

10: liquid crystal cell

11: upper polarizer

12: lower polarizer

13: protective film

14: backlight unit

Hereinafter, preferred embodiments of the present invention will be described. However, embodiments of the present invention may be modified in various other forms, and the scope of the present invention is not limited to the embodiments described below. Moreover, embodiment of this invention is provided in order to demonstrate this invention in detail to the person skilled in the art.

An exemplary embodiment of the present application, the acrylate resin; Phase transition regulator having a glass transition temperature (Tg) of 130 ° C. or higher; And a retardation film comprising a composition comprising a triazine birefringence control agent or a cured product thereof, wherein the triazine birefringence control agent is included in an amount of 5 parts by weight or more and 15 parts by weight or less based on 100 parts by weight of the acrylate resin. To provide.

In the present specification, the glass transition temperature was measured using METTLER DSC (Differential Scanning Calorymeter) equipment, and the measuring method is 3 mg to 20 mg of the resin to be measured in an aluminum crucible and 30 ° C. to 250 ° C. of 10 ° C. per minute. The resin is melted at a temperature rising rate, cooled to 30 ° C. again, and then melted at a temperature rising rate of 10 ° C. per minute up to 200 ° C. again. At this time, through the METTLER DSC equipment, the middle point of the temperature range in which the resin changes the specific heat behavior during the second melting process is measured, this value is measured as the glass transition temperature value.

In one embodiment of the present application, the acrylate resin may include a (meth) acrylate resin having a weight average molecular weight of 100,000 g / mol to 5 million g / mol.

The said weight average molecular weight is one of the average molecular weights whose molecular weight is not uniform and the molecular weight of a certain polymeric material is used as a reference, and is a value obtained by averaging the molecular weight of the component molecular species of the polymeric compound with molecular weight distribution in a weight fraction.

The weight average molecular weight can be measured through Gel Permeation Chromatography (GPC) analysis.

In the present specification, (meth) acrylate is meant to include both acrylates and methacrylates. The (meth) acrylate resin may be, for example, a copolymer of a (meth) acrylic acid ester monomer and a crosslinkable functional group-containing monomer.

Although the said (meth) acrylic acid ester monomer is not specifically limited, For example, alkyl (meth) acrylate is mentioned, More specifically, it is a monomer which has a C1-C12 alkyl group, A pentyl (meth) acrylate, n-butyl (meth) acrylate, ethyl (meth) acrylate, methyl (meth) acrylate, hexyl (meth) acrylate, n-octyl (meth) acrylate, isooctyl (meth) acrylate, 2-ethyl It may include one or more types of hexyl (meth) acrylate, dodecyl (meth) acrylate and decyl (meth) acrylate.

The crosslinkable functional group-containing monomer is not particularly limited, but may include, for example, one or more types of hydroxy group-containing monomers, carboxyl group-containing monomers and nitrogen-containing monomers.

Examples of the hydroxyl group-containing compound include 2-hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate, 4-hydroxybutyl (meth) acrylate, 6-hydroxyhexyl (meth ) Acrylate, 8-hydroxyoctyl (meth) acrylate, 2-hydroxyethylene glycol (meth) acrylate, 2-hydroxypropylene glycol (meth) acrylate, etc. are mentioned.

Examples of the carboxyl group-containing compound include (meth) acrylic acid, 2- (meth) acryloyloxyacetic acid, 3- (meth) acryloyloxypropyl acid, 4- (meth) acryloyloxybutyl acid, acrylic acid double Sieve, itaconic acid, maleic acid, or maleic anhydride.

Examples of the nitrogen-containing monomers include (meth) acrylonitrile, N-vinyl pyrrolidone, N-vinyl caprolactam, and the like.

At least one of vinyl acetate, styrene and acrylonitrile may be further copolymerized with the (meth) acrylate resin in view of other functionalities such as compatibility.

In one embodiment of the present application, the acrylate-based resin may be polymethyl methacrylate (PMMA, Poly methylmethacrylate).

In an exemplary embodiment of the present application, the phase difference regulator having a glass transition temperature of 130 ° C. or higher may be a phase difference regulator including a styrene monomer.

In another exemplary embodiment, the phase difference regulator having a glass transition temperature of 130 ° C. or more may be a styrene-maleic anhydride (SMA) copolymer.

In an exemplary embodiment of the present application, the retardation modifier is a styrene-maleic anhydride (SMA) copolymer, and may have a glass transition temperature of 134 ° C.

The said copolymer is called a copolymer obtained by superposing | polymerizing 2 or more types of other monomers, and, as for a copolymer, 2 or more types of units may be arrange | positioned irregularly or regularly.

The copolymer may be a random copolymer having random forms of monomers mixed with each other, a block copolymer in which blocks arranged in a predetermined section are repeated, or alternating forms in which monomers are alternately repeated and polymerized. There may be a copolymer (Alternating Copolymer), the phase difference regulator having a glass transition temperature of 130 ℃ or more according to an embodiment of the present application may be an irregular copolymer, a block copolymer or an alternating copolymer.

In the present application, the glass transition temperature of the retardation film composition is increased by using a phase difference regulator having a glass transition temperature of 130 ° C. or higher, thereby having particularly excellent heat resistance.

In the case of the retardation film composition of the present application, polymethyl methacrylate (PMMA, Polymethylmethacrylate) having a low glass transition temperature is used as the acrylate resin, and thus, Styrene-maleic anhydride (SMA) having a low glass transition temperature is used. The glass transition temperature of styrene-maleic anhydride (SMA) used at this time is 130 ° C or higher to increase the glass transition temperature of the retardation film composition as a whole. have. In addition, the triazine-based birefringent modifier added together is effective in improving wavelength dispersion, but has a disadvantage in lowering the glass transition temperature, so the role of styrene-maleic anhydride (SMA) is very important in the present application. Do.

In an exemplary embodiment of the present application, the retardation modifier may be included in an amount of 15 parts by weight or more and 85 parts by weight or less based on 100 parts by weight of the acrylate-based resin.

In another exemplary embodiment, the phase difference regulator may be included in an amount of 20 parts by weight or more and 83 parts by weight or less, preferably 30 parts by weight or more and 82 parts by weight or less, based on 100 parts by weight of the acrylate-based resin.

When the retardation agent is included in the above range, in the retardation film, it has a feature that can implement the reverse wavelength / flat wavelength dispersion by changing the wavelength dispersion to a suitable range. In addition, when the content of the retardation regulator exceeds the weight part of the above range, the glass transition temperature of the retardation film composition may have a disadvantage that the heat resistance is poor.

In an exemplary embodiment of the present application, the triazine-based birefringence modifier provides a retardation film that is contained in 5 parts by weight or more and 15 parts by weight or less based on 100 parts by weight of the acrylate-based resin.

In another exemplary embodiment, the triazine-based birefringence modifier may be included in an amount of 5.5 parts by weight or more and 14 parts by weight or less, preferably 6 parts by weight or more and 13 parts by weight or less, based on 100 parts by weight of the acrylate resin.

In the present application, in the case of the triazine-based birefringent regulator included in the retardation film, it is not intended to be used for general UV blocking purposes, but to change the wavelength dispersibility by using a refractive index difference with an acrylic resin.

When the triazine-based birefringence control agent is included in the content range, the wavelength dispersion of the retardation film may be lowered to 1.01 or less to realize flat / reverse dispersion in general forward dispersion, and have excellent optical characteristics. When the weight part of the triazine-based birefringence modifier is smaller than the above range, the wavelength dispersion property has a normal dispersion rather than the flat dispersion / reverse dispersion, and when more than the above range, the phase difference expression becomes small, making it difficult to express sufficient phase difference. Has

That is, when the triazine-based birefringence control agent exceeds the above range, the wavelength dispersion is low but the glass transition temperature (Tg) is very low, the retardation expression is also very low, thereby having a disadvantage that the thickness of the film must be very thick. do.

In one embodiment of the present application, the triazine-based birefringence modifier may be used a 2-hydroxyphenyl-s-triazine derivative (2-hydroxyphenyl-s-triazine derivative), specifically, BASF Tinuvin 1600, Tinuvin 460 , Tinuvin477, Tinuvin479, Tinuvin1577 and / or ADEKA LA-F70, LA46 and the like, but is not limited thereto.

In one embodiment of the present application, the triazine-based birefringence modifier may be represented by the following formula (1).

[Formula 1]

In Chemical Formula 1,

L ₁ to L ₃ are the same as or different from each other, and each independently a direct bond; Substituted or unsubstituted arylene group; Or a substituted or unsubstituted heteroarylene group,

Z ₁ to Z ₃ are the same as or different from each other, and each independently hydrogen; Hydroxyl group; Substituted or unsubstituted alkoxy group; Substituted or unsubstituted alkyl group; Substituted or unsubstituted aryl group; Or a substituted or unsubstituted heteroaryl group.

a, b, and c are the same as or different from each other, and each independently an integer of 1 to 3,

p, q and r are the same as or different from each other, and each independently an integer of 1 to 5. When a, b, c, p, q and r are integers of 2 or more, the substituents in the two or more parentheses are the same or different from each other.

Examples of the substituents are described below, but are not limited thereto.

As used herein, the term "substituted or unsubstituted" refers to an alkoxy group; An alkyl group; Aryl group; And it is substituted or unsubstituted with one or more substituents selected from the group consisting of a heterocyclic group, or substituted or unsubstituted two or more substituents of the substituents exemplified above. For example, "a substituent to which two or more substituents are linked" may be a biphenyl group. That is, the biphenyl group may be an aryl group or may be interpreted as a substituent to which two phenyl groups are linked.

In the present specification, the alkyl group may be linear or branched chain, carbon number is not particularly limited, but is preferably 1 to 40. According to an exemplary embodiment, the alkyl group has 1 to 20 carbon atoms. According to another exemplary embodiment, the alkyl group has 1 to 10 carbon atoms. According to another exemplary embodiment, the alkyl group has 1 to 6 carbon atoms. Specific examples of the alkyl group include methyl, ethyl, propyl, n-propyl, isopropyl, butyl, n-butyl, isobutyl, tert-butyl, sec-butyl, 1-methyl-butyl, 1-ethyl-butyl group, pentyl group, n-pentyl group, isopentyl group, neopentyl group, tert-pentyl group, hexyl group, n-hexyl group, 1-methylpentyl group, 2-methylpentyl group, 4- Methyl-2-pentyl group, 3,3-dimethylbutyl group, 2-ethylbutyl group, heptyl group, n-heptyl group, 1-methylhexyl group, cyclopentylmethyl group, cyclohexylmethyl group, octyl group, n-octyl group , tert-octyl group, 1-methylheptyl group, 2-ethylhexyl group, 2-propylpentyl group, n-nonyl group, 2,2-dimethylheptyl group, 1-ethyl-propyl group, 1,1-dimethyl- Propyl group, isohexyl group, 4-methylhexyl group, 5-methylhexyl group and the like, but is not limited thereto.

In the present specification, the alkoxy group may be linear, branched or cyclic. Although carbon number of an alkoxy group is not specifically limited, It is preferable that it is C1-C40. Specifically, methoxy, ethoxy, n-propoxy, isopropoxy, i-propyloxy, n-butoxy, isobutoxy, tert-butoxy, sec-butoxy, n-pentyloxy, neopentyloxy, Isopentyloxy, n-hexyloxy, 3,3-dimethylbutyloxy, 2-ethylbutyloxy, n-octyloxy, n-nonyloxy, n-decyloxy, benzyloxy, p-methylbenzyloxy and the like It may be, but is not limited thereto.

Substituents comprising alkyl groups, alkoxy groups and other alkyl group moieties described herein include both straight and pulverized forms.

In the present specification, the aryl group is not particularly limited, but preferably has 6 to 60 carbon atoms, and may be a monocyclic aryl group or a polycyclic aryl group. According to an exemplary embodiment, the aryl group has 6 to 30 carbon atoms. According to an exemplary embodiment, the aryl group has 6 to 20 carbon atoms. The aryl group may be a monocyclic aryl group, but may be a phenyl group, a biphenyl group, a terphenyl group, etc., but is not limited thereto. The polycyclic aryl group may be a naphthyl group, anthracenyl group, phenanthryl group, pyrenyl group, perylenyl group, triphenyl group, chrysenyl group, fluorenyl group, and the like, but is not limited thereto.

In the present specification, the heterocyclic group is a heterocyclic group including one or more of N, O, P, S, Si, and Se as hetero atoms, and carbon number is not particularly limited, but is preferably 1 to 60 carbon atoms. According to an exemplary embodiment, the heterocyclic group has 1 to 30 carbon atoms. Examples of the heterocyclic group include, for example, pyridyl group, pyrrole group, pyrimidyl group, pyridazinyl group, furanyl group, thiophenyl group, imidazole group, pyrazole group, oxazole group, isoxazole group, thiazole group, isothiazole group, Triazole group, oxadiazole group, thiadiazole group, dithiazole group, tetrazole group, pyranyl group, thiopyranyl group, pyrazinyl group, oxazinyl group, thiazinyl group, deoxyyl group, triazinyl group, tetrazinyl group, quinone Nolinyl group, isoquinolinyl group, quinolyl group, quinazolinyl group, quinoxalinyl group, naphthyridinyl group, acriridyl group, xanthenyl group, phenanthridinyl group, diazanphthalenyl group, triazainyl group, indole group , Indolinyl group, indolinyl group, phthalazinyl group, pyrido pyrimidinyl group, pyrido pyrazinyl group, pyrazino pyrazinyl group, benzothiazole group, benzoxazole group, benzimidazole group, benzothiophene group , Benzofuranyl group, dibenzothiophenyl group, dibenzofuranyl , Carbazole group, benzocarbazole group, dibenzocarbazole group, indolocarbazole group, indenocarbazole group, phenazinyl group, imidazopyridine group, phenoxazinyl group, phenanthridine group, phenanthroline group, phenanthroline group, phenanthroline group Phenothiazine, imidazopyridine and imidazophenanthridine groups. Although there exists a benzoimidazoquinazoline group or a benzoimidazophenanthridine group, it is not limited only to these.

In the present specification, the description of the aforementioned hetero ring group may be applied except that the heteroaryl group is aromatic.

In the present specification, the description of the aryl group described above may be applied except that the arylene is a divalent group.

In one embodiment of the present application, the L _{One To} L ₃ Is a direct bond; Or a substituted or unsubstituted arylene group having 6 to 60 carbon atoms.

In another exemplary embodiment, L ₁ to L ₃ are a direct bond; Or a substituted or unsubstituted arylene group having 6 to 40 carbon atoms.

In another exemplary embodiment, L ₁ to L ₃ are a direct bond; Or a phenylene group.

In one embodiment of the present application, Z ₁ to Z ₃ is hydrogen; Hydroxyl group; Substituted or unsubstituted aryl group having 6 to 60 carbon atoms; Or a substituted or unsubstituted alkoxy group.

In another exemplary embodiment, Z ₁ to Z ₃ are hydrogen; Hydroxyl group; Substituted or unsubstituted aryl group having 6 to 40 carbon atoms; Or a substituted or unsubstituted alkoxy group.

In another exemplary embodiment, Z ₁ to Z ₃ are hydrogen; Hydroxyl group; Aryl groups having 6 to 40 carbon atoms; Or an alkoxy group unsubstituted or substituted with an alkyl group having 1 to 40 carbon atoms.

In another exemplary embodiment, Z ₁ to Z ₃ are hydrogen; Hydroxyl group; Phenyl group; It may be an alkoxy group unsubstituted or substituted with a branched alkyl group having 1 to 10 carbon atoms.

In one embodiment of the present application, Chemical Formula 1 may be represented by the following Chemical Formula 2.

[Formula 2]

In Formula 2, the definitions of Z ₁ to Z ₃ , p, q, and r are the same as the definitions in Formula 1 above.

In one embodiment of the present application, at least one of Z ₁ to Z ₃ may be a substituted or unsubstituted aryl group.

Particularly, when at least one of Z ₁ to Z ₃ has a phenyl group, a difference in birefringence is greater than that at other cases, and due to the structural difference of the triazine-based birefringence regulator, Z ₁ to Z ₃ do not have a phenyl group. Even when a true birefringence modulator is overfilled, the effect is small.

In particular, in one embodiment of the present application, when using a BASF Tinuvin 1600 (2-hydroxyphenyl-s-triazine derivative) as a triazine-based birefringent modifier, the effect of improving the wavelength dispersion is the largest compared to the similar content, which is It may be due to the birefringence difference due to the structural difference.

Acrylate resins according to the present application; A phase difference regulator comprising a styrene monomer having a glass transition temperature of 130 ° C. or higher; And the content and composition of the triazine-based birefringent modifier can be identified through the analysis of nuclear magnetic resonance (NMR, Nuclear magnetic resonace) and gas chromatography (GC, Gas Chromatography).

In an exemplary embodiment of the present application, a dichroism value in the wavelength range of 200 nm to 400 nm of the triazine-based birefringence modulator provides a phase difference film that satisfies Equation 1 below.

[Equation 1]

0.01 ≤ ㅣ α _e -α ₀ ㅣ ≤ 0.05

In the formula 1,

α _e is the extinction coefficient of extraordinary ray,

α ₀ is an absorption coefficient of ordinary ray.

In the present invention, the extinction coefficient α _e of the extraordinary ray and the extinction coefficient α ₀ of the ordinary ray can be calculated by measuring the polarization transmittance of the film containing the triazine-based birefringence control agent. For example, a polarizing plate is attached to a light source of a transmittance measuring device (for example, Hitachi U-3310, etc.) to generate polarized light, and then the polarized light is transmitted through a sample film to measure transmittance T _o of normal light. , The polarized light is transmitted in the state where the sample film is rotated 90 degrees, and the transmittance T _e of the abnormal light is measured. Then, the absorbance coefficients of the ordinary light and the abnormal light can be calculated by substituting the measured ordinary light transmittance and the abnormal light transmittance into the following equation.

-Log T = αbc

(T: transmittance, α: extinction coefficient, b: sample thickness, c: triazine birefringence regulator concentration)

In another exemplary embodiment, the value of dichroism in the wavelength range of 200 nm to 400 nm of the triazine-based birefringent modulator is 0.02 ≦ ㅣ α _e -α ₀ ㅣ ≤ 0.04, preferably 0.025 ≦ ㅣ α _e -α ₀ | ≤ 0.04 may be satisfied.

In an exemplary embodiment of the present application, the retardation film provides a retardation film that satisfies the following Expressions 2 and 3.

[Equation 2]

0.7 ≤ R _in (450) / R _in (550) ≤ 1.0

[Equation 3]

1.0 ≤ R _in (650) / R _in (550) ≤ 1.2

In Formula 2 and Formula 3,

R _in (λ) is the plane retardation at a wavelength λnm, is a value of (n _x -n _y ) xd,

N _x is a refractive index in a slow axis direction of the retardation film surface,

N _y is a refractive index in the fast axis direction of the retardation film surface,

D is the thickness of the retardation film.

In Equation 2 and Equation 3, R _in (λ) is a surface direction retardation measured at a wavelength of λ nm, and the measurement is a value measured using Axoscan of Axometrics. That is, in Equation 2 and Equation 3, R _in (450), R _in (550) and R _in (650) mean surface direction retardation values at 450 nm, 550 nm and 650 nm, respectively.

The plane direction retardation at each wavelength is determined by the difference between the refractive index in the slow axis direction and the refractive index in the fast axis direction and the thickness of the retardation film, as described in Expressions 2 and 3 above. to be. The slow axis and fast axis are determined by the orientation direction of the polymer chain of the retardation film. The direction in which the polymer chain is oriented is called the slow axis. The slow axis takes the longest time for light to pass through and has the greatest retardation delay. Fast axis is the opposite concept. The fast axis is the direction in which the polymer chain is oriented in a small direction. It is called the fast axis.

In Equation 2, the surface direction retardation at a wavelength of 550 nm may be referred to as R _in (550), and the surface direction retardation at a wavelength of 450 nm may be referred to as R _in (450). When R _in (450) / R _in (550), which is a phase difference ratio between two wavelengths, is 1 or less, it is called reverse wavelength dispersion. When 1, flat wavelength dispersion is greater than 1, it indicates constant wavelength dispersion.

Similarly to Equation 2, Equation 3 also shows reverse wavelength dispersion / flat wavelength dispersion when R _in (650) / R _in (550) has the range of Equation 3.

In addition, in an exemplary embodiment of the present application, the retardation film provides a retardation film that satisfies the following formula 4 and formula 5.

[Equation 4]

0nm ≤ R _in (550) ≤ 150nm

[Equation 5]

40nm ≤ R _th (550) ≤ 150nm

In Formula 4 and Formula 5,

R _in (550) is the plane retardation at a wavelength of 550 nm, is a value of (n _x -n _y ) xd,

R _th (550) is a thickness retardation at a wavelength of 550 nm, and is a value of {n _z- (n _x + n _y ) / 2} xd,

N _x is a refractive index in a slow axis direction of the retardation film surface,

N _y is a refractive index in the fast axis direction of the retardation film surface,

N _z is a refractive index in the retardation film thickness direction,

D is the thickness of the retardation film.

In Equations 4 and 5, R _in (λ) is a surface direction retardation measured at a wavelength of λ nm, and the measurement is a value measured using Axoscan, Axometrics. In addition, R _th (λ) is a phase difference in the thickness direction at a wavelength of λ nm, the refractive index in the thickness direction is measured by AxoScan equipment, and is a value determined by the value of the difference with the average of the refractive indices in the plane direction and the thickness.

In one embodiment of the present application, the thickness of the retardation film is 10 ㎛ or more and 100 ㎛ It may be:

In another exemplary embodiment, the thickness of the retardation film is 10 μm or more and 100 μm Or less, Preferably it is 15 micrometers or more and 95 micrometers Or less, More preferably, it is 15 micrometers or more and 80 micrometers It may be:

As can be seen from the equations 2 to 5, the retardation value changes according to the thickness of the retardation film, and in the present application, when the thickness of the retardation film has the above range, it has a flat dispersion / reverse dispersion.

In one embodiment of the present application, the glass transition temperature of the composition of the retardation film may be 118 ℃ or more.

The glass transition temperature of the composition is 118 ℃ or more means, acrylate resin; A phase difference regulator having a glass transition temperature of 130 ° C. or higher; And it means a glass transition temperature for the composition comprising a triazine-based birefringent control agent, the measuring method is the same as described above.

In one embodiment of the present application, the glass transition temperature of the composition of the retardation film may be 118 ℃ or more, preferably 120 ℃ or more.

In one embodiment of the present application, the glass transition temperature of the composition of the retardation film may be 150 ° C or less, preferably 130 ° C or less.

In the case of the retardation film according to the present application, the glass transition temperature value of the composition, including a phase difference regulator having a glass transition temperature of 130 ° C or more, can maintain the above range, according to the retardation film has a very excellent heat resistance characteristics .

In one embodiment of the present application, the retardation film of the wavelength dispersion of the retardation film is 0.1 or more and 1.01 or less.

In another exemplary embodiment, the wavelength dispersion of the retardation film may be 0.1 or more and 1.01 or less, preferably 0.6 or more and 1.01 or less.

On the other hand, the manufacturing method of the retardation film of the present invention having the characteristics as described above is not particularly limited, it may be prepared by a method of forming the film after forming the composition, and stretching it.

The composition is prepared by, for example, extruding and kneading the mixture obtained after preblending the film raw material with any suitable mixer such as an omni mixer. In this case, the mixer used for extrusion kneading is not specifically limited, For example, any suitable mixer, such as an extruder, such as a single screw extruder and a twin screw extruder, and a pressurized kneader, can be used.

As a method of the said film shaping | molding, arbitrary suitable film shaping | molding methods, such as the solution casting method (solution casting method), the melt-extrusion method, the calender method, the compression molding method, are mentioned, for example. Among these film forming methods, a solution cast method (solution casting method) and a melt extrusion method are preferable.

As a solvent used for the said solution casting method (solution casting method), For example, aromatic hydrocarbons, such as benzene, toluene, xylene; Aliphatic hydrocarbons such as cyclohexane and decalin; Esters such as ethyl acetate and butyl acetate; Ketones such as acetone, methyl ethyl ketone and methyl isobutyl ketone; Alcohols such as methanol, ethanol, isopropanol, butanol, isobutanol, methyl cellosolve, ethyl cellosolve and butyl cellosolve; Ethers such as tetrahydrofuran and dioxane; Halogenated hydrocarbons such as dichloromethane, chloroform and carbon tetrachloride; Dimethylformamide; Dimethyl sulfoxide, etc. are mentioned. These solvents may be used independently or may use 2 or more types together.

As an apparatus for performing the said solution casting method (solution casting method), a drum type casting machine, a band type casting machine, a spin coater, etc. are mentioned, for example. In addition, as said melt-extrusion method, the T-die method, the inflation method, etc. are mentioned, for example. Molding temperature may be 150 ℃ to 350 ℃, or 200 ℃ to 300 ℃.

When forming a film by the said T die method, a T die can be attached to the front-end | tip of a well-known single screw extruder or a twin screw extruder, the film extruded in film shape can be rolled, and a roll-shaped film can be obtained.

After the film is formed through the above process, the film is stretched. The stretching step may be performed in the longitudinal direction (MD) stretching or in the transverse direction (TD) stretching, or both. In addition, in the case where both longitudinal stretching and transverse stretching are performed, either stretching may be performed first and then stretching in the other direction, or both directions may be simultaneously stretched. In addition, the stretching may be performed in one step, or may be carried out in multiple steps. In the case of longitudinal stretching, stretching by the speed difference between the rolls can be performed, and in the case of transverse stretching, a tenter can be used. The starting angle of the tenter is usually within 10 degrees, which suppresses the bowing phenomenon occurring during the lateral stretching and regularly controls the angle of the optical axis. Even when the transverse stretching is carried out in multiple stages, the anti-boeing effect can be obtained.

It is preferable that extending | stretching temperature is a range near the glass transition temperature of the composition which is a film raw material, and when the glass transition temperature of the said composition is Tg, Preferably it is (Tg-30 degreeC)-(Tg + 100 degreeC), More Preferably it is (Tg-20 degreeC)-(Tg + 80 degreeC), More preferably, it exists in the range of (Tg-5 degreeC)-(Tg + 20 degreeC). If the stretching temperature is less than (Tg-30 占 폚), there is a fear that a sufficient stretching ratio may not be obtained. On the contrary, when extending | stretching temperature exceeds (Tg + 100 degreeC), the flow (flow) of a resin composition arises and there exists a possibility of not being able to perform stable extending | stretching.

In addition, in an exemplary embodiment of the present application, the stretching ratio in the stretching of the film may be 1.05 to 10 times based on the length in the stretching direction.

In addition, the total draw ratio may be stretched to be 1.1 times or more, or 1.2 times or more, or 1.5 times or more, 25 times or less, or 10 times or less, or 7 times or less based on the total stretching area of the base film. When the draw ratio is less than 1.1 times, the effect of stretching may not be sufficiently achieved, and when the draw ratio is greater than 25 times, the film layer may be cracked.

Before the stretching, a process of flattening the coated surface of the composition and drying to volatilize the solvent included in the composition may be performed.

The retardation film may be subjected to heat treatment (annealing) or the like after the stretching treatment in order to stabilize its optical isotropy and mechanical properties. The heat treatment conditions are not particularly limited and may employ any suitable conditions known to those skilled in the art.

The retardation film of the present invention as described above can be usefully applied to a polarizing plate and / or a liquid crystal display device. In one embodiment of the present invention, the present invention is a polarizer; And it provides a polarizing plate comprising at least one retardation film of the present application.

1 is a diagram illustrating a laminated structure of a polarizing plate 103 according to an exemplary embodiment of the present application. Specifically, the polarizing plate 103 has a structure in which the polarizer 102 and the retardation film 101 are stacked on one surface of the polarizer.

In one embodiment of the present application, the polarizer is not particularly limited, and a film made of polyvinyl alcohol (PVA) containing a polarizer well known in the art, for example, iodine or a dichroic dye, is used.

The polarizer exhibits a property of extracting only light vibrating in one direction from incident light while vibrating in various directions. This property can be achieved by stretching polyvinyl alcohol (PVA) absorbing iodine with strong tension. For example, more specifically, swelling by swelling the PVA film in an aqueous solution, dyeing with a dichroic substance imparting polarization to the swelled PVA film, stretching the dyed PVA film. The polarizer may be formed through a stretching step of arranging the dichroic dye materials side by side in the stretching direction, and a complementary color step of correcting the color of the PVA film subjected to the stretching step. However, the polarizing plate of the present invention is not limited thereto.

In one embodiment of the present application, the polarizer and the retardation film may be adhered with an adhesive or a pressure-sensitive adhesive, the adhesive can be used as long as it is known in the art is not particularly limited. For example, there are water-based adhesives, one-component or two-component polyvinyl alcohol (PVA) adhesives, polyurethane adhesives, epoxy adhesives, styrene butadiene rubber (SBR) adhesives, or hot melt adhesives. It is not limited only to these examples.

The retardation film may be directly attached to one side or both sides of the polarizer. In addition, it is attached to the protective film of the conventional polarizing plate with a protective film on both sides of the polarizer, it can be usefully used as a retardation film.

When the retardation film is directly attached to one side or both sides of the polarizer, for example, the structure may be an upper protective film / polarizer / retardation film or a retardation film / polarizer / low protective film. The attaching method is a roll coater, a gravure coater, a bar coater, a knife coater, a capillary coater, or a micro chamber doctor blade coater and the like to coat the primer on the surface of the retardation film or polarizer, and then , By spraying the adhesive in a dropwise manner, and heating the laminated body including the retardation film and the polarizer with a lamination roll, laminating by pressing at room temperature, or UV curing.

2 is a view showing a laminated structure of a polarizing plate according to an exemplary embodiment of the present application. Specifically, the polarizing plate 103 may have a structure in which a polarizer protective film 104 / an adhesive layer (adhesive layer) 105 / a phase difference film 101 / a polarizer 102 / a polarizer protective film 104 are sequentially stacked. In addition, the polarizer protective film may include a retardation film according to the present application.

In the case of the retardation film according to the exemplary embodiment of the present application, as shown in FIG. 2, the position of the retardation film is positioned in contact with the polarizer, and is not intended to block and absorb ultraviolet rays. It can be confirmed that it has a main purpose.

In an exemplary embodiment of the present application, a polarizer protective film is attached to one surface of the polarizer, and the polarizing plate according to the present application is attached to a surface opposite to the surface on which the polarizer protective film of the polarizer is attached. do.

In one embodiment of the present application, the polarizing plate may be bonded to the polarizer protective film on the opposite side of the surface in contact with the polarizer of the retardation film, the adhesive may be bonded through the adhesive layer (adhesive layer). .

In one embodiment of the present application, the polarizer protective film is a COP (cycloolefin polymer) film, acrylic film, TAC (triacetylcellulose) film, COC (cycloolefin copolymer) film, PNB (polynorbornene) film and PET (polyethylene) terephtalate) film may be made of any one or more.

In an exemplary embodiment of the present application, a liquid crystal display device including the polarizing plate is provided.

In addition, an exemplary embodiment of the present application is a liquid crystal cell; An upper polarizer provided in an upper layer of the liquid crystal cell; A lower polarizer provided in the lower layer of the liquid crystal cell; And a backlight unit provided under the lower polarizer, wherein at least one of the upper polarizer and the lower polarizer is a polarizer; And a phase difference film according to an exemplary embodiment of the present application disposed on one surface of the polarizer.

In one embodiment of the present application, the upper polarizing plate is the polarizer; And the retardation film, wherein the retardation film is disposed to face the liquid crystal cell.

In one embodiment of the present application, the lower polarizing plate is the polarizer; And the retardation film, wherein the retardation film is disposed to face the backlight unit.

The upper polarizer is the polarizer; And the retardation film, wherein the retardation film is disposed to face the liquid crystal cell, wherein the upper polarizer is the polarizer; And the retardation film, wherein the retardation film is disposed in the liquid crystal cell direction in the liquid crystal display, and specifically, a backlight unit, a lower polarizing plate, a liquid crystal cell, a retardation film, and a polarizer are sequentially stacked. It means having a structure.

The lower polarizer is the polarizer; And the retardation film, wherein the retardation film is disposed to face the backlight unit, wherein the lower polarizer is the polarizer; And the retardation film, wherein the retardation film is disposed in the direction of the backlight unit in the liquid crystal display, and specifically, a backlight unit / polarizer / retardation film / liquid crystal cell / upper polarizing plate is sequentially stacked. It means having a structure.

In the liquid crystal display according to the present application, when the retardation film of the upper polarizing plate is disposed to face the liquid crystal cell, or the retardation film of the lower polarizing plate is disposed to face the backlight unit, included in the retardation film The triazine-based birefringent modulator may have a main purpose to improve the function of the panel by the phase difference expression function, the ultraviolet absorption is not the main function.

The backlight unit includes a light source for irradiating light from the back of the liquid crystal panel, and the type of the light source is not particularly limited, and a general LCD light source such as CCFL, HCFL or LED may be used.

3 is a view showing a liquid crystal display device according to an exemplary embodiment of the present application. Specifically, the upper polarizing plate 11 and the lower polarizing plate 12 may be stacked on both sides of the liquid crystal cell 10, and the surface of the lower polarizing plate 12 adjacent to the backlight unit 14 may be in contact with the liquid crystal cell 10. The protective film 13 may be laminated on the opposite surface. As the upper polarizing plate 11 and the lower polarizing plate 12, a polarizing plate according to an exemplary embodiment of the present application may be used. Preferably, the lower polarizing plate 12 may use a polarizing plate according to an exemplary embodiment of the present application.

The protective film is the same as the content of the polarizer protective film described above.

Hereinafter, the operation and effects of the invention will be described in more detail with reference to specific examples of the invention. However, these embodiments are only presented as an example of the invention, whereby the scope of the invention is not determined.

< Example >

Preparation of the composition

The components and weight ratios of the compositions used in the Examples and Comparative Examples herein are shown in Table 1 below.

	Acrylate Resin (Content)	Phase difference regulator (content)	Triazine birefringence modifier (content)	Dichroic maximum	Glass transition temperature of the composition
Example 1	PMMA (100 parts by weight)	SMA (65.9 parts by weight)	Tinuvin 1600 (7.5 parts by weight)	0.032	121 ℃
Example 2	PMMA (100 parts by weight)	SMA (82.4 parts by weight)	Tinuvin 1600 (9.2 parts by weight)	0.033	122 ℃
Example 3	PMMA (100 parts by weight)	SMA (67.4 parts by weight)	Tinuvin1600 (9.9 parts by weight)	0.037	120 ℃
Example 4	PMMA (100 parts by weight)	SMA (80.2 parts by weight)	Tinuvin 1600 (10.7 parts by weight)	0.036	121 ℃
Example 5	PMMA (100 parts by weight)	SMA (65.9 parts by weight)	LA-F70 (12.6 parts by weight)	0.027	121 ℃
Comparative Example 1	PMMA (100 parts by weight)	SMA (42.9 parts by weight)	-	0	123 ℃
Comparative Example 2	PMMA (100 parts by weight)	SMA (33.3 parts by weight)	-	0	122 ℃
Comparative Example 3	PMMA (100 parts by weight)	SAN (42.9 parts by weight)	-	0	110 ℃
Comparative Example 4	PMMA (100 parts by weight)	SAN (33.3 parts by weight)	-	0	112 ℃
Comparative Example 5	PMMA (100 parts by weight)	SMA (64.4 parts by weight)	Tinuvin 1600 (4.8 parts by weight)	0.022	123 ℃
Comparative Example 6	PMMA (100 parts by weight)	SMA (53.8 parts by weight)	Tinuvin 1600 (3.1 parts by weight)	0.014	124 ℃

In Table 1, as the triazine-based birefringent regulator, Tinuvin 1600 from BASF or LA-F70 from ADEKA was used.

About the composition which has the composition and weight ratio of the said Table 1, it extended | stretched according to the conditions of the following Table 2, and produced the retardation film.

	Drawing temperature	Elongation Ratio (MD / TD)
Example 1	Tg + 7 ℃	1.35 / 3.55
Example 2	Tg + 7 ℃	1.35 / 3.55
Example 3	Tg + 7 ℃	1.35 / 3.55
Example 4	Tg + 7 ℃	1.35 / 3.55
Example 5	Tg + 7 ℃	1.35 / 3.55
Comparative Example 1	Tg + 7 ℃	1.35 / 3.5
Comparative Example 2	Tg + 7 ℃	1.35 / 3.5
Comparative Example 3	Tg + 9 ℃	1.35 / 3.45
Comparative Example 4	Tg + 9 ℃	1.35 / 3.45
Comparative Example 5	Tg + 7 ℃	1.35 / 3.5
Comparative Example 6	Tg + 7 ℃	1.35 / 3.5

The results of measuring film properties and heat resistance of the retardation films of Examples 1 to 5 and Comparative Examples 1 to 6 are shown in Table 3 below.

	Film properties
	Rin / Rth	RD450 / RD650
Example 1	121/120	0.946 / 1.002
Example 2	120/120	0.948 / 1.002
Example 3	110/111	0.934 / 1.004
Example 4	116/115	0.942 / 1.002
Example 5	123/121	0.959 / 1.001
Comparative Example 1	119/118	1.060 / 0.969
Comparative Example 2	105/104	1.059 / 0.969
Comparative Example 3	123/121	1.059 / 0.967
Comparative Example 4	105/105	1.061 / 0.969
Comparative Example 5	125/124	1.017 / 0.984
Comparative Example 6	127/127	1.037 / 0.974

In Examples 1 to 5 of Table 3, it was confirmed that the wavelength dispersion was shown as the reverse wavelength dispersion and the glass transition temperature was high due to the sufficient amount of the SMA and the triazine-based birefringence regulator. On the other hand, Comparative Examples 1 and 2 used SMA, but there was no triazine-based birefringence modifier, so the glass transition temperature was high, but the wavelength dispersion showed a constant wavelength dispersion. In Comparative Examples 3 and 4, the glass transition temperature was used as the phase difference regulator. Low styrene-acrylonitrile (Styrene-Acrylonitrile, SAN) was used to confirm that the low glass transition temperature appears.

Particularly, in Examples 1 to 4 of Table 3, when Tinuvin1600 manufactured by BASF is used as a triazine-based birefringence modifier, the number of benzene rings in the molecule is large (at least one of Z ₁ to Z ₃ in the general formula (1) is a phenyl group). In the case of), it was confirmed that the difference in birefringence is particularly excellent in the stretching process. That is, in Example 5 of Table 3, in order to show a similar effect to the case of adding Tinuvin1600 manufactured by BASF as the triazine-based birefringence regulator, it can be seen that in Example 5, a higher content of triazine-based birefringence regulator is used. have. This is due to the difference in the structure of the two triazine-based birefringent modulators.

In the case of Comparative Examples 5 and 6, the SMA is sufficiently used, so that the glass transition temperature is high, but the content range of the triazine-based birefringence regulator is small, so that the wavelength dispersion is not sufficiently lowered, and unlike the retardation film of the present invention, it shows a constant wavelength dispersion I could confirm it.

In addition, if the triazine-based birefringence regulator exceeds 15 parts by weight based on 100 parts by weight of the acrylate-based resin, the wavelength dispersion is lowered, but the glass transition temperature (Tg) is very low, resulting in poor durability of the film and very low retardation. Could. For example, if the triazine birefringent regulator (Tinuvin1600) is 16 parts by weight and the phase difference regulator (SMA) is 60 parts by weight, the glass transition temperature value will be lowered to about 115 ° C. In addition, the retardation expression was very low, it was confirmed that the disadvantage that the thickness of the film should be made very thick.

Claims (14)

1. Acrylate resins;

   Phase transition regulator having a glass transition temperature (Tg) of 130 ° C. or higher; And

   Retardation film comprising a composition containing a triazine-based birefringent control agent or a cured product thereof,

   The triazine-based birefringence control agent is a retardation film is contained in 5 parts by weight or more and 15 parts by weight or less based on 100 parts by weight of the acrylate resin.
2. The method according to claim 1,

   Retardation film wherein the value of dichroism in the wavelength range of 200nm to 400nm of the triazine-based birefringence regulator satisfies the following formula 1:

   [Equation 1]

   0.01 ≤ ㅣ α _e -α ₀ ㅣ ≤ 0.05

   In the formula 1,

   α _e is the extinction coefficient of extraordinary ray,

   α ₀ is an absorption coefficient of ordinary ray.
3. The method according to claim 1,

   The retardation film is 130 ℃ or more phase difference modifier is a styrene-maleic anhydride (SMA) copolymer.
4. The method according to claim 1,

   The phase difference regulator, based on 100 parts by weight of the acrylate resin,

   Retardation film is contained in 15 parts by weight or more and 85 parts by weight or less.
5. The method according to claim 1,

   Retardation film which the said retardation film satisfy | fills following formula 2 and formula:

   [Equation 2]

   0.7 ≤ R _in (450) / R _in (550) ≤ 1.0

   [Equation 3]

   1.0 ≤ R _in (650) / R _in (550) ≤ 1.2

   In Formula 2 and Formula 3,

   R _in (λ) is the plane retardation at a wavelength λnm, is a value of (n _x -n _y ) xd,

   N _x is a refractive index in a slow axis direction of the retardation film surface,

   N _y is a refractive index in the fast axis direction of the retardation film surface,

   D is the thickness of the retardation film.
6. The method according to claim 1,

   Retardation film which the said retardation film satisfy | fills following formula 4 and formula:

   [Equation 4]

   0nm ≤ R _in (550) ≤ 150nm

   [Equation 5]

   40nm ≤ R _th (550) ≤ 150nm

   In Formula 4 and Formula 5,

   R _in (550) is the plane retardation at a wavelength of 550 nm, is a value of (n _x -n _y ) xd,

   R _th (550) is a thickness retardation at a wavelength of 550 nm, and is a value of {n _z- (n _x + n _y ) / 2} xd,

   N _x is a refractive index in a slow axis direction of the retardation film surface,

   N _y is a refractive index in the fast axis direction of the retardation film surface,

   N _z is a refractive index in the retardation film thickness direction,

   D is the thickness of the retardation film.
7. The method according to claim 1,

   The thickness of the retardation film is 10 µm or more and 100 µm Retardation film which is the following.
8. The method according to claim 1,

   The glass transition temperature of the composition is more than 118 ℃ retardation film.
9. The method according to claim 1,

   The retardation film of which wavelength dispersion property of the said retardation film is 0.1 or more and 1.01 or less.
10. Polarizer; And

    The polarizing plate containing at least one or more retardation films of any one of Claims 1-9.
11. The method according to claim 10,

    A polarizer protective film is attached to one surface of the polarizer,

    The retardation film is attached to the surface opposite to the surface attached to the polarizer protective film of the polarizer.
12. Liquid crystal cell;

    An upper polarizer provided in an upper layer of the liquid crystal cell;

    A lower polarizer provided in the lower layer of the liquid crystal cell; And

    It includes a backlight unit provided on the lower layer of the lower polarizing plate,

    At least one of the upper polarizer and the lower polarizer is a polarizer; And a phase difference film of any one of claims 1 to 9 disposed on one surface of the polarizer.
13. The method according to claim 12,

    The upper polarizer is the polarizer; And the retardation film,

    And the retardation film is disposed to face the liquid crystal cell.
14. The method according to claim 12,

    The lower polarizer is the polarizer; And the retardation film,

    And the retardation film is disposed to face the backlight unit.

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