WO2018066199A1 - Optical laminate and image display device - Google Patents

Abstract

Provided is an optical laminate which is suppressed in cracking of a conductive layer under high temperature high humidity conditions. An optical laminate according to the present invention sequentially comprises, in the following order: a polarizing plate which contains a polarizer and a protective layer that is disposed on at least one surface of the polarizer; a first retardation layer; a second retardation layer; a conductive layer; and a substrate which is closely adhered onto the conductive layer. The substrate has a water vapor permeability of from 5 mg/m²·24h to 10 mg/m²·24h, a dimensional change rate of 0.3% or less, and a linear expansion coefficient of from 5 (× 10^-6/°C) to 10 (× 10^-6/°C).

Description

Optical laminate and image display device

The present invention relates to an optical laminate and an image display device using the same.

In recent years, with the spread of thin displays, displays (organic EL display devices) equipped with organic EL panels have been proposed. Since the organic EL panel has a highly reflective metal layer, problems such as external light reflection and background reflection tend to occur. Thus, it is known to prevent these problems by providing a circularly polarizing plate on the viewing side. On the other hand, there is an increasing demand for so-called inner touch panel type input display devices in which a touch sensor is incorporated between a display cell (for example, an organic EL cell) and a polarizing plate. Since the input display device having such a configuration has a short distance between the image display cell and the touch sensor, it is possible to give the user a natural feeling of input operation.

In the polarizing plate (or circularly polarizing plate) for the inner touch panel type input display device, the polarizing plate (or circularly polarizing plate) and the conductivity for the touch sensor are used from the viewpoints of thinning, prevention of variation in quality, and improvement of manufacturing efficiency. Integration with film is under consideration. However, the polarizing plate in which the conductive film for the touch sensor is integrated has a problem that cracks are easily generated in the conductive layer of the conductive film under high temperature and high humidity.

JP 2003-311239 A JP 2002-372622 A Japanese Patent No. 3325560 JP 2003-036143 A

The present invention has been made to solve the above-described conventional problems, and a main object thereof is to provide an optical laminate in which cracking of a conductive layer under high temperature and high humidity is suppressed.

The optical layered body of the present invention includes a polarizer, a polarizing plate including a protective layer on at least one side of the polarizer, a first retardation layer, a second retardation layer, a conductive layer, And a base material closely laminated on the conductive layer in this order. In this optical laminate, the substrate has a moisture permeability of 5 mg / m ² · 24 h to 10 mg / m ² · 24 h, a dimensional change rate of 0.3% or less, and a linear expansion coefficient of 5 ( × 10 ⁻⁶ / ° C.) to 10 (× 10 ⁻⁶ / ° C.).
In one embodiment, the angle formed by the absorption axis of the polarizer and the slow axis of the first retardation layer is 10 ° to 20 °, and the absorption axis and the second retardation layer are The angle formed with the slow axis is 65 ° to 85 °.
In one embodiment, the 1st phase contrast layer and the 2nd phase contrast layer are constituted by cyclic olefin system resin film. In this case, the dimensional change rate of the second retardation layer is, for example, 1% or less.
In another embodiment, the first retardation layer and the second retardation layer are alignment solidified layers of a liquid crystal compound. In this case, the dimensional change rate of the laminate of the polarizing plate, the first retardation layer, and the second retardation layer is, for example, 1% or less.
According to another aspect of the present invention, an image display device is provided. This image display device includes the optical laminate described above.

According to the present invention, in an optical laminate having a polarizing plate, two retardation layers, and a conductive layer for touch sensor, the moisture permeability, dimensional change rate, and linear expansion coefficient of the substrate laminated in close contact with the conductive layer are optimized. As a result, the occurrence of cracks in the conductive layer under high temperature and high humidity can be significantly suppressed. As a result, it is possible to realize an optical laminate having very excellent durability.

It is a schematic sectional drawing of the optical laminated body by one Embodiment of this invention.

Hereinafter, embodiments of the present invention will be described, but the present invention is not limited to these embodiments.

(Definition of terms and symbols)
The definitions of terms and symbols in this specification are as follows.
(1) Refractive index (nx, ny, nz)
“Nx” is the refractive index in the direction in which the in-plane refractive index is maximum (ie, the slow axis direction), and “ny” is the direction orthogonal to the slow axis in the plane (ie, the fast axis direction). “Nz” is the refractive index in the thickness direction.
(2) In-plane retardation (Re)
“Re (λ)” is an in-plane retardation measured with light having a wavelength of λ nm at 23 ° C. For example, “Re (550)” is an in-plane retardation measured with light having a wavelength of 550 nm at 23 ° C. Re (λ) is determined by the formula: Re (λ) = (nx−ny) × d, where d (nm) is the thickness of the layer (film).
(3) Thickness direction retardation (Rth)
“Rth (λ)” is a retardation in the thickness direction measured with light having a wavelength of λ nm at 23 ° C. For example, “Rth (550)” is a retardation in the thickness direction measured with light having a wavelength of 550 nm at 23 ° C. Rth (λ) is determined by the formula: Rth (λ) = (nx−nz) × d, where d (nm) is the thickness of the layer (film).
(4) Nz coefficient The Nz coefficient is obtained by Nz = Rth / Re.

A. FIG. 1 is a schematic cross-sectional view of an optical laminate according to one embodiment of the present invention. The optical laminated body 100 of this embodiment has the polarizing plate 10, the 1st phase difference layer 20, the 2nd phase difference layer 30, the conductive layer 41, and the base material 42 in this order. The polarizing plate 10 includes a polarizer 11, a first protective layer 12 disposed on one side of the polarizer 11, and a second protective layer 13 disposed on the other side of the polarizer 11. . Depending on the purpose, one of the first protective layer 12 and the second protective layer 13 may be omitted. For example, when the first retardation layer 20 can also function as a protective layer for the polarizer 11, the second protective layer 13 may be omitted. The base material 42 is closely adhered to the conductive layer 41. In the present specification, “adhesion lamination” means that two layers are directly and firmly laminated without an adhesive layer (for example, an adhesive layer or an adhesive layer). Each of the conductive layer 41 and the base material 42 may be a component of the optical laminate 100 as a single layer, or may be introduced into the optical laminate 100 as a laminate of the base material 42 and the conductive layer 41. In addition, in order to make it easy to see, the ratio of the thickness of each layer in drawing differs from actual.

In the embodiment of the present invention, the moisture permeability of the base material 42 is 5 mg / m ² · 24 h to 10 mg / m ² · 24 h, preferably 6 mg / m ² · 24 h to 9 mg / m ² · 24 h, More preferably, it is 7 mg / m ² · 24 h to 8 mg / m ² · 24 h. The dimensional change rate of the base material 42 is 0.3% or less, preferably 0.1% or less, and more preferably 0.05% or less. Further, the linear expansion coefficient of the base material 42 is 5 (× 10 ⁻⁶ / ° C.) to 10 (× 10 ⁻⁶ / ° C.), preferably 6 (× 10 ⁻⁶ / ° C.) to 9 (× 10 ^{− 6} / ° C.), more preferably 7 (× 10 ⁻⁶ / ° C.) to 8 (× 10 ⁻⁶ / ° C.). By providing a base material closely laminated on the conductive layer, and further optimizing by combining the above characteristics of the base material, the occurrence of cracks in the conductive layer under high temperature and high humidity can be remarkably suppressed. The moisture permeability can be determined based on the moisture permeability test (cup method) of JIS Z0208. The dimensional change rate refers to the dimensional change rate when placed in an environment of a temperature of 85 ° C. and a relative humidity of 85% for 240 hours. The linear expansion coefficient can be determined by TMA measurement according to JIS K 7197.

In one embodiment, the first retardation layer 20 and the second retardation layer 30 are each made of a resin film. In another embodiment, the first retardation layer 20 and the second retardation layer 30 may each be an alignment solidified layer of a liquid crystal compound. The resin film will be described in detail in the sections C-2 and D-2, and the alignment solidified layer of the liquid crystal compound will be described in detail in the sections C-3 and D-3.

Each layer constituting the optical laminate other than the adhesion lamination of the conductive layer 41 and the substrate 42 may be laminated via any appropriate adhesive layer (adhesive layer or pressure-sensitive adhesive layer: not shown). In addition, as in the case of the conductive layer 41 and the base material 42, they may be closely stacked.

The optical layered body preferably has a dimensional change rate of 1% or less, more preferably 0.95% or less. The smaller the dimensional change rate of the optical laminate, the better. The lower limit of the dimensional change rate of the optical laminated body is, for example, 0.01%. If the dimensional change rate of the optical laminate is in such a range, the occurrence of cracks in the conductive layer under high temperature and high humidity can be remarkably suppressed.

The total thickness of the optical laminated body is preferably 220 μm or less, more preferably 80 μm to 190 μm. When the first retardation layer 20 and the second retardation layer 30 are alignment solidified layers of a liquid crystal compound, the total thickness of the optical laminate is preferably 175 μm or less, more preferably 80 μm to 140 μm. is there.

The optical layered body may have a long shape (for example, a roll shape) or a single wafer shape.

Hereinafter, each layer, optical film, and pressure-sensitive adhesive constituting the optical laminate will be described in more detail.

B. Polarizing plate B-1. Polarizer Any appropriate polarizer may be adopted as the polarizer 11. For example, the resin film forming the polarizer may be a single-layer resin film or a laminate of two or more layers.

Specific examples of polarizers composed of a single-layer resin film include hydrophilic polymer films such as polyvinyl alcohol (PVA) films, partially formalized PVA films, and ethylene / vinyl acetate copolymer partially saponified films. In addition, there may be mentioned polyene-based oriented films such as those subjected to dyeing treatment and stretching treatment with dichroic substances such as iodine and dichroic dyes, PVA dehydrated products and polyvinyl chloride dehydrochlorinated products. Preferably, a polarizer obtained by dyeing a PVA film with iodine and uniaxially stretching is used because of excellent optical properties.

The dyeing with iodine is performed, for example, by immersing a PVA film in an aqueous iodine solution. The stretching ratio of the uniaxial stretching is preferably 3 to 7 times. The stretching may be performed after the dyeing treatment or may be performed while dyeing. Moreover, you may dye | stain after extending | stretching. If necessary, the PVA film is subjected to swelling treatment, crosslinking treatment, washing treatment, drying treatment and the like. For example, by immersing the PVA film in water and washing it before dyeing, not only can the surface of the PVA film be cleaned of dirt and anti-blocking agents, but the PVA film can be swollen to cause uneven staining. Can be prevented.

As a specific example of a polarizer obtained by using a laminate, a laminate of a resin substrate and a PVA resin layer (PVA resin film) laminated on the resin substrate, or a resin substrate and the resin Examples thereof include a polarizer obtained by using a laminate with a PVA resin layer applied and formed on a substrate. For example, a polarizer obtained by using a laminate of a resin base material and a PVA resin layer applied and formed on the resin base material may be obtained by, for example, applying a PVA resin solution to a resin base material and drying it. A PVA-based resin layer is formed thereon to obtain a laminate of a resin base material and a PVA-based resin layer; the laminate is stretched and dyed to make the PVA-based resin layer a polarizer; obtain. In the present embodiment, stretching typically includes immersing the laminate in an aqueous boric acid solution and stretching. Further, the stretching may further include, if necessary, stretching the laminate in the air at a high temperature (for example, 95 ° C. or higher) before stretching in the boric acid aqueous solution. The obtained resin base material / polarizer laminate may be used as it is (that is, the resin base material may be used as a protective layer of the polarizer), and the resin base material is peeled from the resin base material / polarizer laminate. Any appropriate protective layer according to the purpose may be laminated on the release surface. Details of a method for manufacturing such a polarizer are described in, for example, Japanese Patent Application Laid-Open No. 2012-73580. This publication is incorporated herein by reference in its entirety.

The thickness of the polarizer is preferably 18 μm or less, more preferably 1 μm to 12 μm, still more preferably 3 μm to 12 μm, and particularly preferably 5 μm to 12 μm.

The boric acid content of the polarizer is preferably 18% by weight or more, more preferably 18% by weight to 25% by weight. If the content of boric acid in the polarizer is in such a range, the ease of curling adjustment at the time of bonding is well maintained and the curling at the time of heating is achieved by a synergistic effect with the iodine content described later. It is possible to improve the appearance durability during heating while satisfactorily suppressing. The boric acid content can be calculated as the amount of boric acid contained in the polarizer per unit weight using, for example, the following formula from the neutralization method.

The iodine content of the polarizer is preferably 2.1% by weight or more, more preferably 2.1% by weight to 3.5% by weight. If the iodine content of the polarizer is in this range, the curl adjustment at the time of bonding is well maintained and the curl at the time of heating is maintained by a synergistic effect with the boric acid content. It is possible to improve the appearance durability during heating while satisfactorily suppressing. In this specification, “iodine content” means the amount of all iodine contained in a polarizer (PVA resin film). More specifically, iodine exists in the form of iodine ions (I ⁻ ), iodine molecules (I ₂ ), polyiodine ions (I ₃ ⁻ , I ₅ ⁻ ), etc. in the polarizer. Iodine content means the amount of iodine encompassing all these forms. The iodine content can be calculated, for example, by a calibration curve method of fluorescent X-ray analysis. The polyiodine ion exists in a state where a PVA-iodine complex is formed in the polarizer. By forming such a complex, absorption dichroism can be developed in the wavelength range of visible light. Specifically, the complex of PVA and triiodide ions (PVA · I ₃ ⁻ ) has an absorption peak around 470 nm, and the complex of PVA and pentaiodide ions (PVA · I ₅ ⁻ ) is around 600 nm. Have an absorption peak. As a result, polyiodine ions can absorb light in a wide range of visible light depending on their form. On the other hand, iodine ion (I ⁻ ) has an absorption peak near 230 nm and is not substantially involved in the absorption of visible light. Therefore, polyiodine ions present in a complex state with PVA can be mainly involved in the absorption performance of the polarizer.

The polarizer preferably exhibits absorption dichroism at any wavelength between 380 nm and 780 nm. As described above, the single transmittance of the polarizer is 43.0% to 46.0%, preferably 44.5% to 46.0%. The polarization degree of the polarizer is preferably 97.0% or more, more preferably 99.0% or more, and further preferably 99.9% or more.

B-2. First protective layer The first protective layer 12 is formed of any suitable film that can be used as a protective layer for a polarizer. Specific examples of the material as the main component of the film include cellulose resins such as triacetyl cellulose (TAC), polyester-based, polyvinyl alcohol-based, polycarbonate-based, polyamide-based, polyimide-based, polyethersulfone-based, and polysulfone-based materials. And transparent resins such as polystyrene, polynorbornene, polyolefin, (meth) acryl, and acetate. Further, thermosetting resins such as (meth) acrylic, urethane-based, (meth) acrylurethane-based, epoxy-based, and silicone-based or ultraviolet curable resins are also included. In addition to this, for example, a glassy polymer such as a siloxane polymer is also included. Further, a polymer film described in JP-A-2001-343529 (WO01 / 37007) can also be used. As a material for this film, for example, a resin composition containing a thermoplastic resin having a substituted or unsubstituted imide group in the side chain and a thermoplastic resin having a substituted or unsubstituted phenyl group and nitrile group in the side chain For example, a resin composition having an alternating copolymer of isobutene and N-methylmaleimide and an acrylonitrile / styrene copolymer can be mentioned. The polymer film can be, for example, an extruded product of the resin composition.

As will be described later, the optical layered body of the present invention is typically disposed on the viewing side of the image display device, and the first protective layer 12 is typically disposed on the viewing side. Therefore, the first protective layer 12 may be subjected to a surface treatment such as a hard coat treatment, an antireflection treatment, an antisticking treatment, and an antiglare treatment as necessary. Further / or, if necessary, the first protective layer 12 is provided with a treatment for improving visibility when viewed through polarized sunglasses (typically, imparting an (elliptical) circular polarization function, (Giving an ultrahigh phase difference) may be applied. By performing such processing, excellent visibility can be achieved even when the display screen is viewed through a polarizing lens such as polarized sunglasses. Therefore, the optical laminate can be suitably applied to an image display device that can be used outdoors.

As the thickness of the first protective layer, any appropriate thickness can be adopted as long as the difference between the thickness of the desired polarizing plate and the thickness of the second protective layer can be obtained. The thickness of the first protective layer is, for example, 10 μm to 50 μm, preferably 15 μm to 40 μm. In addition, when the surface treatment is performed, the thickness of the first protective layer is a thickness including the thickness of the surface treatment layer.

B-3. Second protective layer The second protective layer 13 is also formed of any suitable film that can be used as a protective layer for the polarizer. The material constituting the main component of the film is as described in the section B-2 regarding the first protective layer. The second protective layer 13 is preferably optically isotropic. In this specification, “optically isotropic” means that the in-plane retardation Re (550) is 0 nm to 10 nm and the thickness direction retardation Rth (550) is −10 nm to +10 nm. Say.

The thickness of the second protective layer is, for example, 15 μm to 35 μm, preferably 20 μm to 30 μm. The difference between the thickness of the first protective layer and the thickness of the second protective layer is preferably 15 μm or less, more preferably 10 μm or less. If the difference in thickness is within such a range, curling at the time of bonding can be satisfactorily suppressed. The thickness of the first protective layer and the thickness of the second protective layer may be the same, the first protective layer may be thicker, and the second protective layer may be thicker. . Typically, the first protective layer is thicker than the second protective layer.

C. First retardation layer C-1. Characteristics of First Retardation Layer The first retardation layer 20 may have any appropriate optical and / or mechanical characteristics depending on the purpose. The first retardation layer 20 typically has a slow axis. In one embodiment, the angle formed by the slow axis of the first retardation layer 20 and the absorption axis of the polarizer 11 is preferably 10 ° to 20 °, more preferably 13 ° to 17 °. More preferably about 15 °. If the angle formed by the slow axis of the first retardation layer 20 and the absorption axis of the polarizer 11 is within such a range, the surfaces of the first retardation layer and the second retardation layer will be described later. By setting the inner phase difference within a predetermined range and arranging the slow axis of the second retardation layer at a predetermined angle with respect to the absorption axis of the polarizer, the circular polarization characteristics (excellent in a wide band ( As a result, an optical laminate having very excellent antireflection properties can be obtained.

The first retardation layer preferably has a relationship in which the refractive index characteristic is nx> ny ≧ nz. The in-plane retardation Re (550) of the first retardation layer is preferably 180 nm to 320 nm, more preferably 200 nm to 290 nm, and further preferably 230 nm to 280 nm. Here, “ny = nz” includes not only the case where ny and nz are completely equal, but also the case where they are substantially equal. Therefore, ny <nz may be satisfied as long as the effects of the present invention are not impaired.

The Nz coefficient of the first retardation layer is preferably 0.9 to 3, more preferably 0.9 to 2.5, still more preferably 0.9 to 1.5, and particularly preferably 0.9 to 1. 3. By satisfying such a relationship, a very excellent reflection hue can be achieved when the obtained optical laminate is used in an image display device.

The first retardation layer may exhibit a reverse dispersion wavelength characteristic in which the retardation value increases according to the wavelength of the measurement light, and has a positive chromatic dispersion characteristic in which the retardation value decreases according to the wavelength of the measurement light. It may also be possible to show a flat chromatic dispersion characteristic in which the phase difference value hardly changes depending on the wavelength of the measurement light. In one embodiment, the first retardation layer exhibits a flat wavelength dispersion characteristic in which the retardation value hardly changes depending on the wavelength of the measurement light. In this case, Re (450) / Re (550) of the retardation layer is preferably from 0.99 to 1.03, and Re (650) / Re (550) is preferably from 0.98 to 1.02. is there. A first retardation layer having a flat chromatic dispersion characteristic and having a predetermined in-plane retardation and a second retardation layer having a flat chromatic dispersion characteristic and having a predetermined in-plane retardation have a predetermined slow axis. By using in combination at an angle, it is possible to realize an excellent antireflection characteristic in a wide band.

The absolute value of the photoelastic coefficient of the first retardation layer is preferably 2 × 10 ⁻¹¹ m ² / N or less, more preferably 2.0 × 10 ⁻¹³ m ² / N to 1.5 × 10 ^−11. m ² / N, more preferably from ^{1.0 × 10 -12 m 2 /N~1.2×10 -11} m 2 / N resin. When the absolute value of the photoelastic coefficient is in such a range, a phase difference change is unlikely to occur when a shrinkage stress is generated during heating. As a result, heat unevenness of the obtained image display apparatus can be prevented satisfactorily.

C-2. First retardation layer composed of resin film When the first retardation layer is composed of a resin film, the thickness is preferably 60 μm or less, and preferably 30 μm to 50 μm. If the thickness of the first retardation layer is in such a range, a desired in-plane retardation can be obtained.

The first retardation layer 20 can be composed of any appropriate resin film that can satisfy the characteristics described in the above section C-1. Typical examples of such resins include cyclic olefin resins, polycarbonate resins, cellulose resins, polyester resins, polyvinyl alcohol resins, polyamide resins, polyimide resins, polyether resins, polystyrene resins, acrylic resins. Based resins. When the first retardation layer is formed of a resin film that exhibits flat wavelength characteristics, a cyclic olefin-based resin can be suitably used.

The cyclic olefin-based resin is a general term for resins that are polymerized using a cyclic olefin as a polymerization unit, and is described in, for example, JP-A-1-240517, JP-A-3-14882, JP-A-3-122137, and the like. Resin. Specific examples include ring-opening (co) polymers of cyclic olefins, addition polymers of cyclic olefins, copolymers of cyclic olefins and α-olefins such as ethylene and propylene (typically random copolymers). And graft modified products in which these are modified with an unsaturated carboxylic acid or a derivative thereof, and hydrides thereof. Specific examples of the cyclic olefin include norbornene monomers. Examples of the norbornene-based monomer include norbornene and alkyl and / or alkylidene substituted products thereof such as 5-methyl-2-norbornene, 5-dimethyl-2-norbornene, 5-ethyl-2-norbornene, 5-butyl- 2-Norbornene, 5-ethylidene-2-norbornene, etc. Polar group substitution products such as halogens; dicyclopentadiene, 2,3-dihydrodicyclopentadiene, etc .; dimethanooctahydronaphthalene, alkyl and / or alkylidene substitution thereof And polar group substituents such as halogen, for example, 6-methyl-1,4: 5,8-dimethano-1,4,4a, 5,6,7,8,8a-octahydronaphthalene, 6-ethyl -1,4: 5,8-dimethano-1,4,4a, 5,6,7,8,8a-octahi Lonaphthalene, 6-ethylidene-1,4: 5,8-dimethano-1,4,4a, 5,6,7,8,8a-octahydronaphthalene, 6-chloro-1,4: 5,8-dimethano -1,4,4a, 5,6,7,8,8a-octahydronaphthalene, 6-cyano-1,4: 5,8-dimethano-1,4,4a, 5,6,7,8,8a -Octahydronaphthalene, 6-pyridyl-1,4: 5,8-dimethano-1,4,4a, 5,6,7,8,8a-octahydronaphthalene, 6-methoxycarbonyl-1,4: 5 8-Dimethano-1,4,4a, 5,6,7,8,8a-octahydronaphthalene and the like; Tripentamers of cyclopentadiene such as 4,9: 5,8-dimethano-3a, 4 4a, 5,8,8a, 9,9a-Octahydro-1H-benzoindene 4,11: 5,10: 6,9 Torimetano -3a, 4,4a, 5,5a, 6,9,9a, 10,10a, 11,11a- dodecahydro -1H- cyclopentadiene anthracene, and the like.

In the present invention, other cycloolefins capable of ring-opening polymerization can be used in combination as long as the object of the present invention is not impaired. Specific examples of such cycloolefins include compounds having one reactive double bond such as cyclopentene, cyclooctene, and 5,6-dihydrodicyclopentadiene.

The cyclic olefin resin preferably has a number average molecular weight (Mn) measured by a gel permeation chromatograph (GPC) method using a toluene solvent, preferably 25,000 to 200,000, more preferably 30,000 to 100,000. 000, most preferably 40,000 to 80,000. When the number average molecular weight is in the above range, a material having excellent mechanical strength, good solubility, moldability, and casting operability can be obtained.

When the cyclic olefin-based resin is obtained by hydrogenating a ring-opening polymer of a norbornene monomer, the hydrogenation rate is preferably 90% or more, more preferably 95% or more, Most preferably, it is 99% or more. Within such a range, the heat deterioration resistance and light deterioration resistance are excellent.

A commercially available film may be used as the cyclic olefin resin film. Specific examples include trade names “ZEONEX” and “ZEONOR” manufactured by ZEON CORPORATION, “Arton” manufactured by JSR, “TOPAS” trade name manufactured by TICONA, and trade names manufactured by Mitsui Chemicals, Inc. “APEL” may be mentioned.

The first retardation layer 20 is obtained, for example, by stretching a film formed from the above cyclic olefin resin. Any appropriate molding method can be adopted as a method of forming a film from a cyclic olefin-based resin. Specific examples include compression molding methods, transfer molding methods, injection molding methods, extrusion molding methods, blow molding methods, powder molding methods, FRP molding methods, cast coating methods (for example, casting methods), calendar molding methods, and hot presses. Law. Extrusion molding or cast coating is preferred. This is because the smoothness of the resulting film can be improved and good optical uniformity can be obtained. The molding conditions can be appropriately set according to the composition and type of the resin used, the properties desired for the retardation layer, and the like. In addition, as above-mentioned, since many film products are marketed for cyclic olefin resin, you may use the said commercial film for an extending | stretching process as it is.

The thickness of the resin film (unstretched film) can be set to any appropriate value depending on the desired thickness of the first retardation layer, the desired optical properties, the stretching conditions described below, and the like. The thickness is preferably 50 μm to 300 μm.

Any appropriate stretching method and stretching conditions (for example, stretching temperature, stretching ratio, stretching direction) may be employed for the stretching. Specifically, various stretching methods such as free end stretching, fixed end stretching, free end contraction, and fixed end contraction can be used singly or simultaneously or sequentially. The stretching direction can also be performed in various directions and dimensions such as a length direction, a width direction, a thickness direction, and an oblique direction. The stretching temperature is preferably Tg-30 ° C. to Tg + 60 ° C., more preferably Tg-10 ° C. to Tg + 50 ° C. with respect to the glass transition temperature (Tg) of the resin film.

A retardation film having the desired optical characteristics (for example, refractive index characteristics, in-plane retardation, Nz coefficient) can be obtained by appropriately selecting the stretching method and stretching conditions.

In one embodiment, the retardation film is produced by uniaxially stretching a resin film or uniaxially stretching a fixed end. As a specific example of the fixed end uniaxial stretching, there is a method of stretching in the width direction (lateral direction) while running the resin film in the longitudinal direction. The draw ratio is preferably 1.1 to 3.5 times.

In another embodiment, the retardation film can be produced by continuously stretching a long resin film obliquely in a direction at a predetermined angle with respect to the longitudinal direction. By adopting oblique stretching, a long stretched film having an orientation angle of a predetermined angle with respect to the longitudinal direction of the film (slow axis in the direction of the angle) can be obtained. For example, lamination with a polarizer At this time, roll-to-roll is possible, and the manufacturing process can be simplified. The angle may be an angle formed between the absorption axis of the polarizer and the slow axis of the first retardation layer in the optical layered body. As described above, the angle is preferably 10 ° to 20 °, more preferably 13 ° to 17 °, and further preferably about 15 °.

Examples of the stretching machine used for the oblique stretching include a tenter type stretching machine capable of adding feed forces, pulling forces, or pulling forces at different speeds in the lateral and / or longitudinal directions. The tenter type stretching machine includes a horizontal uniaxial stretching machine, a simultaneous biaxial stretching machine, and the like, but any suitable stretching machine can be used as long as a long resin film can be continuously stretched obliquely.

By appropriately controlling the left and right velocities in the stretching machine, the first retardation layer (substantially having the desired in-plane retardation and having the slow axis in the desired direction). , A long retardation film) can be obtained.

The stretching temperature of the film can vary depending on the in-plane retardation value and thickness desired for the first retardation layer, the type of resin used, the thickness of the film used, the stretching ratio, and the like. Specifically, the stretching temperature is preferably Tg-30 ° C to Tg + 30 ° C, more preferably Tg-15 ° C to Tg + 15 ° C, and most preferably Tg-10 ° C to Tg + 10 ° C. By extending | stretching at such temperature, the 1st phase difference layer which has a suitable characteristic in this invention can be obtained. Tg is the glass transition temperature of the constituent material of the film.

C-3. First Retardation Layer Consists of Liquid Crystal Compound Alignment Solidified Layer The first retardation layer 20 may be a liquid crystal compound alignment solidified layer. By using the liquid crystal compound, the difference between nx and ny of the obtained retardation layer can be remarkably increased as compared with the non-liquid crystal material. Therefore, the first retardation for obtaining a desired in-plane retardation is obtained. The thickness of the layer can be significantly reduced. As a result, the optical laminate can be further reduced in thickness. When the first retardation layer 20 is composed of an alignment solidified layer of a liquid crystal compound, the thickness is preferably 1 μm to 7 μm, more preferably 1.5 μm to 2.5 μm. By using the liquid crystal compound, an in-plane retardation equivalent to that of the resin film can be realized with a thickness much thinner than that of the resin film.

In the present specification, the “alignment solidified layer” refers to a layer in which a liquid crystal compound is aligned in a predetermined direction in the layer and the alignment state is fixed. The “alignment solidified layer” is a concept including an alignment cured layer obtained by curing a liquid crystal monomer as described later. In the present embodiment, typically, rod-like liquid crystal compounds are aligned in a state where they are aligned in the slow axis direction of the first retardation layer (homogeneous alignment). Examples of the liquid crystal compound include a liquid crystal compound (nematic liquid crystal) whose liquid crystal phase is a nematic phase. As such a liquid crystal compound, for example, a liquid crystal polymer or a liquid crystal monomer can be used. The liquid crystal compound may exhibit liquid crystallinity either lyotropic or thermotropic. The liquid crystal polymer and the liquid crystal monomer may be used alone or in combination.

When the liquid crystal compound is a liquid crystal monomer, the liquid crystal monomer is preferably a polymerizable monomer and a crosslinkable monomer. This is because the alignment state of the liquid crystal monomer can be fixed by polymerizing or crosslinking (that is, curing) the liquid crystal monomer. After aligning the liquid crystal monomers, for example, if the liquid crystal monomers are polymerized or cross-linked, the alignment state can be fixed thereby. Here, a polymer is formed by polymerization and a three-dimensional network structure is formed by crosslinking, but these are non-liquid crystalline. Accordingly, in the formed first retardation layer, for example, transition to a liquid crystal phase, a glass phase, or a crystal phase due to a temperature change specific to the liquid crystal compound does not occur. As a result, the first retardation layer is an extremely stable retardation layer that is not affected by temperature changes.

The temperature range in which the liquid crystal monomer exhibits liquid crystal properties varies depending on its type. Specifically, the temperature range is preferably 40 ° C. to 120 ° C., more preferably 50 ° C. to 100 ° C., and most preferably 60 ° C. to 90 ° C.

Any appropriate liquid crystal monomer can be adopted as the liquid crystal monomer. For example, the polymerizable mesogenic compounds described in JP-T-2002-533742 (WO00 / 37585), EP358208 (US521118), EP66137 (US4388453), WO93 / 22397, EP0266172, DE195504224, DE44081171, and GB2280445 can be used. Specific examples of such a polymerizable mesogenic compound include, for example, trade name LC242 of BASF, trade name E7 of Merck, and trade name LC-Silicon-CC3767 of Wacker-Chem. As the liquid crystal monomer, for example, a nematic liquid crystal monomer is preferable.

The alignment solidified layer of the liquid crystal compound is subjected to an alignment treatment on the surface of a predetermined substrate, and a coating liquid containing the liquid crystal compound is applied to the surface to align the liquid crystal compound in a direction corresponding to the alignment treatment, It can be formed by fixing the alignment state. By using such an alignment treatment, the liquid crystal compound can be aligned in a predetermined direction with respect to the long direction of the long substrate, and as a result, the liquid crystal compound is delayed in the predetermined direction of the formed retardation layer. A phase axis can be developed. For example, a retardation layer having a slow axis in a direction of 15 ° with respect to the longitudinal direction can be formed on a long substrate. Such a retardation layer can be laminated using roll-to-roll even when it is desired to have a slow axis in an oblique direction, so the productivity of the optical laminate is greatly improved. Can do. In one embodiment, the substrate is any suitable resin film, and the alignment solidified layer formed on the substrate can be transferred to the surface of the polarizing plate 10. In another embodiment, the substrate can be the second protective layer 13. In this case, the transfer step is omitted, and the lamination can be performed by roll-to-roll continuously from the formation of the alignment solidified layer (first retardation layer), so that the productivity is further improved.

Any appropriate alignment treatment can be adopted as the alignment treatment. Specifically, a mechanical alignment process, a physical alignment process, and a chemical alignment process are mentioned. Specific examples of the mechanical alignment treatment include rubbing treatment and stretching treatment. Specific examples of the physical alignment process include a magnetic field alignment process and an electric field alignment process. Specific examples of the chemical alignment treatment include oblique vapor deposition and photo-alignment treatment. Arbitrary appropriate conditions may be employ | adopted for the process conditions of various orientation processes according to the objective.

The alignment of the liquid crystal compound is performed by processing at a temperature showing a liquid crystal phase according to the type of the liquid crystal compound. By performing such a temperature treatment, the liquid crystal compound takes a liquid crystal state, and the liquid crystal compound is oriented according to the orientation treatment direction of the substrate surface.

In one embodiment, the alignment state is fixed by cooling the liquid crystal compound aligned as described above. When the liquid crystal compound is a polymerizable monomer or a crosslinkable monomer, the alignment state is fixed by subjecting the liquid crystal compound aligned as described above to a polymerization treatment or a crosslinking treatment.

Specific examples of the liquid crystal compound and details of the method of forming the alignment solidified layer are described in JP-A No. 2006-163343. The description in this publication is incorporated herein by reference.

D. Second retardation layer D-1. Characteristics of Second Retardation Layer The second retardation layer 30 may have any appropriate optical and / or mechanical characteristics depending on the purpose. The second retardation layer 30 typically has a slow axis. In one embodiment, the angle formed by the slow axis of the second retardation layer 30 and the absorption axis of the polarizer 11 is preferably 65 ° to 85 °, more preferably 72 ° to 78 °. More preferably about 75 °. The angle formed by the slow axis of the second retardation layer 30 and the slow axis of the first retardation layer 20 is preferably 52 ° to 68 °, more preferably 57 ° to 63 °. More preferably, it is about 60 °. If the angle formed by the slow axis of the second retardation layer 30 and the absorption axis of the polarizer 11 is within such a range, the in-plane retardation of the first retardation layer is set within a predetermined range as described above. The slow axis of the first retardation layer is arranged at a predetermined angle with respect to the absorption axis of the polarizer, and the in-plane retardation of the second retardation layer is set within a predetermined range as will be described later. By setting, it is possible to obtain an optical layered body having a very excellent circular polarization characteristic (as a result, a very excellent antireflection characteristic) in a wide band.

The second retardation layer preferably has a relationship of refractive index characteristics of nx> ny ≧ nz. The in-plane retardation Re (550) of the second retardation layer is preferably 80 nm to 200 nm, more preferably 100 nm to 180 nm, and still more preferably 110 nm to 170 nm.

Other characteristics of the second retardation layer are as described in the above section C-1 regarding the first retardation layer.

D-2. Second Retardation Layer Constructed of Resin Film When the second retardation layer is composed of a resin film, the thickness is preferably 40 μm or less, and preferably 25 μm to 35 μm. If the thickness of the second retardation layer is within such a range, a desired in-plane retardation can be obtained. When the second retardation layer is formed of a resin film, the material, characteristics, manufacturing method, and the like are as described in the above section C-2 for the first retardation layer.

D-3. Second Retardation Layer Consists of Liquid Crystal Compound Alignment / Solidification Layer The second retardation layer 30 may be a liquid crystal compound alignment / solidification layer in the same manner as the first retardation layer. When the second retardation layer 30 is composed of an alignment solidified layer of a liquid crystal compound, the thickness is preferably 0.5 μm to 2 μm, more preferably 1 μm to 1.5 μm. When the second retardation layer is composed of an alignment solidified layer of a liquid crystal compound, the material, characteristics, manufacturing method, and the like are as described in the above section C-3 for the first retardation layer.

D-4. Combination of first retardation layer and second retardation layer The first retardation layer and the second retardation layer may be used as any appropriate combination. Specifically, the first retardation layer may be composed of a resin film, and the second retardation layer may be composed of an alignment solidified layer of a liquid crystal compound; the first retardation layer is aligned and solidified of a liquid crystal compound. And the second retardation layer may be composed of a resin film; both the first retardation layer and the second retardation layer may be composed of a resin film; Both the phase difference layer and the second phase difference layer may be composed of an alignment solidified layer of a liquid crystal compound. Preferably, when the first retardation layer is composed of a resin film, the second retardation layer is also composed of a resin film; the first retardation layer is composed of an alignment solidified layer of a liquid crystal compound. In some cases, the second retardation layer is also composed of an alignment solidified layer of a liquid crystal compound. When both the first retardation layer and the second retardation layer are made of a resin film, the first retardation layer and the second retardation layer may be the same, and the detailed configuration May be different. The same applies to the case where both the first retardation layer and the second retardation layer are composed of an alignment solidified layer of a liquid crystal compound.

When both the first retardation layer and the second retardation layer are formed of a resin film, the dimensional change rate of the second retardation layer is preferably 1% or less, more preferably 0.95. % Or less. The smaller the dimensional change rate of the second retardation layer, the better. The lower limit of the dimensional change rate of the second retardation layer is, for example, 0.01%. When the dimensional change rate of the second retardation layer is within such a range, the occurrence of cracks in the conductive layer under high temperature and high humidity can be significantly suppressed.

When each of the first retardation layer and the second retardation layer is composed of an alignment solidified layer of a liquid crystal compound, the dimensions of the laminate of the polarizing plate, the first retardation layer, and the second retardation layer The rate of change is preferably 1% or less, more preferably 0.95% or less. The smaller the dimensional change rate of the laminate, the better. The lower limit of the dimensional change rate of the laminate is, for example, 0.01%. When the dimensional change rate of the laminate is within such a range, the occurrence of cracks in the conductive layer under high temperature and high humidity can be remarkably suppressed.

E. Conductive layer The conductive layer can be formed on a metal oxide film on any suitable substrate by any suitable film formation method (eg, vacuum deposition, sputtering, CVD, ion plating, spraying, etc.). Can be formed. After film formation, heat treatment (for example, 100 ° C. to 200 ° C.) may be performed as necessary. By performing the heat treatment, the amorphous film can be crystallized. Examples of the metal oxide include indium oxide, tin oxide, zinc oxide, indium-tin composite oxide, tin-antimony composite oxide, zinc-aluminum composite oxide, and indium-zinc composite oxide. The indium oxide may be doped with divalent metal ions or tetravalent metal ions. Indium composite oxides are preferable, and indium-tin composite oxide (ITO) is more preferable. Indium composite oxides are characterized by high transmittance (for example, 80% or more) in the visible light region (380 nm to 780 nm) and low surface resistance per unit area.

When the conductive layer contains a metal oxide, the thickness of the conductive layer is preferably 50 nm or less, more preferably 35 nm or less. The lower limit of the thickness of the conductive layer is preferably 10 nm.

The surface resistance value of the conductive layer is preferably 300Ω / □ or less, more preferably 150Ω / □ or less, and further preferably 100Ω / □ or less.

The conductive layer can be patterned as needed. By conducting the patterning, a conductive portion and an insulating portion can be formed. Any appropriate method can be adopted as the patterning method. Specific examples of the patterning method include a wet etching method and a screen printing method.

F. Base material Any appropriate resin film may be used as the base material as long as the desired moisture permeability, dimensional change rate, and linear expansion coefficient described in the above section A are obtained. Preferably, the resin film has excellent transparency in addition to the above desired characteristics. Specific examples of the constituent material include a cyclic olefin resin, a polycarbonate resin, a cellulose resin, a polyester resin, and an acrylic resin.

Preferably, the substrate is optically isotropic. Examples of the material constituting the optically isotropic substrate (isotropic substrate) include, for example, a material having a main skeleton such as a norbornene-based resin or an olefin-based resin, a lactone ring, or glutar Examples thereof include materials having a cyclic structure such as an imide ring in the main chain of the acrylic resin. When such a material is used, when an isotropic substrate is formed, it is possible to suppress the expression of the phase difference accompanying the orientation of the molecular chain.

The thickness of the substrate is preferably 10 μm to 200 μm, more preferably 20 μm to 60 μm.

If necessary, a hard coat layer (not shown) may be provided between the conductive layer 41 and the base material 42. As the hard coat layer, a hard coat layer having any appropriate configuration can be used. The thickness of the hard coat layer is, for example, 0.5 μm to 2 μm. If the haze is in an allowable range, fine particles for reducing Newton rings may be added to the hard coat layer. Furthermore, if necessary, the anchor coat layer for improving the adhesion of the conductive layer and / or the reflectance is adjusted between the conductive layer 41 and the base material 42 (a hard coat layer if present). A refractive index adjustment layer may be provided. Arbitrary appropriate structures may be employ | adopted as an anchor coat layer and a refractive index adjustment layer. The anchor coat layer and the refractive index adjusting layer can be thin layers of several nm to several tens of nm.

If necessary, another hard coat layer may be provided on the side opposite to the conductive layer of the base material 42 (outermost side of the optical laminate). The hard coat layer typically includes a binder resin layer and spherical particles, and the spherical particles protrude from the binder resin layer to form convex portions. Details of such a hard coat layer are described in JP-A-2013-145547, and the description of the gazette is incorporated herein by reference.

G. Others The optical layered body according to the embodiment of the present invention may further include other retardation layers. The optical characteristics (for example, refractive index characteristics, in-plane retardation, Nz coefficient, photoelastic coefficient), thickness, arrangement position, and the like of other retardation layers can be appropriately set according to the purpose.

Practically, an adhesive layer (not shown) for bonding to the display cell is provided on the surface of the base material 42. It is preferable that a release film is bonded to the surface of the pressure-sensitive adhesive layer until the optical layered body is used.

H. Image Display Device The optical layered body described in the items A to G can be applied to an image display device. Therefore, the present invention includes an image display device using such an optical laminate. Typical examples of the image display device include a liquid crystal display device and an organic EL display device. An image display device according to an embodiment of the present invention includes the optical layered body described in the items A to G on the viewing side. The optical laminated body is laminated so that the conductive layer is on the display cell (for example, liquid crystal cell, organic EL cell) side (so that the polarizer is on the viewing side). That is, the image display device according to the embodiment of the present invention can be a so-called inner touch panel type input display device in which a touch sensor is incorporated between a display cell (for example, a liquid crystal cell or an organic EL cell) and a polarizing plate. In this case, the touch sensor can be disposed between the conductive layer (or the conductive layer with the base material) and the display cell. As the configuration of the touch sensor, a configuration well known in the industry can be adopted, and a detailed description thereof will be omitted.

Hereinafter, the present invention will be specifically described by way of examples, but the present invention is not limited to these examples. In addition, the measuring method of each characteristic is as follows.

(1) Thickness The applied retardation layer (alignment solidified layer of liquid crystal compound) was measured by an interference film thickness measurement method using MCPD2000 manufactured by Otsuka Electronics. The other films were measured using a digital micrometer (KC-351C manufactured by Anritsu).
(2) Retardation value of retardation layer Refractive index nx, ny and nz of the retardation layer used in the examples and comparative examples were determined using an automatic birefringence measuring device (manufactured by Oji Scientific Instruments, automatic birefringence meter KOBRA- WPR). The measurement wavelength of the in-plane retardation Re was 450 nm and 550 nm, the measurement wavelength of the thickness direction retardation Rth was 550 nm, and the measurement temperature was 23 ° C.
(3) Moisture permeability Measured according to JIS K 7129B (Mocon method). In an atmosphere of a temperature of 40 ° C. and a humidity of 92% RH, the amount of water vapor (mg) passing through a sample having an area of 1 m ² in 24 hours was measured.
(4) Dimensional change rate The base material or retardation layer used in the examples and comparative examples, or the optical laminates obtained in the examples and comparative examples were cut into 100 mm × 100 mm and used as measurement samples. The dimensions after the measurement sample was stored in an oven at a temperature of 85 ° C. and a relative humidity of 85% for 240 hours were measured, and the rate of change from the size before the oven was charged was taken as the dimensional change rate.
(5) Coefficient of linear expansion Using TMA (SS7100) manufactured by SII Nanotechnology, the base materials used in Examples and Comparative Examples were cut into approximately 6 mm squares and placed on a sample table, in accordance with JIS K 7197. TMA (compression expansion method) measurement was performed. The measurement load is 19.6 mN, the probe diameter is 3.5 mmφ, and the rate of temperature rise is 5 ° C / min. The measurement is performed in the range of -150 ° C to 20 ° C. The coefficient was calculated.
(6) Durability of optical laminated body The optical laminated body obtained by the Example and the comparative example was cut out to 100 mm x 50 mm, and was bonded together to the alkali free glass, and it was set as the measurement sample. The measurement sample was stored in an oven at a temperature of 85 ° C. and a relative humidity of 85% for 120 hours. Thereafter, the measurement sample was taken out of the oven, the state of the conductive layer was observed with a laser microscope, and evaluated according to the following criteria.
Good: No cracks were observed. Bad: Significant cracks were observed.

[Reference Example 1: Production of polarizing plate]
A long roll of polyvinyl alcohol (PVA) resin film (product name “PE3000”, manufactured by Kuraray Co., Ltd.) having a thickness of 30 μm is uniaxially stretched in the longitudinal direction so that it becomes 5.9 times in the longitudinal direction by a roll stretching machine. At the same time, swelling, dyeing, crosslinking, and washing treatment were performed, and finally a drying treatment was performed to produce a polarizer 1 having a thickness of 12 μm.
Specifically, the swelling treatment was stretched 2.2 times while being treated with pure water at 20 ° C. Next, the dyeing treatment is performed in an aqueous solution at 30 ° C. in which the weight ratio of iodine and potassium iodide is 1: 7, the iodine concentration of which is adjusted so that the single transmittance of the obtained polarizer is 45.0%. The film was stretched 1.4 times. Furthermore, the crosslinking treatment employed a two-stage crosslinking treatment, and the first-stage crosslinking treatment was stretched 1.2 times while being treated in an aqueous solution in which boric acid and potassium iodide were dissolved at 40 ° C. The boric acid content of the aqueous solution of the first-stage crosslinking treatment was 5.0% by weight, and the potassium iodide content was 3.0% by weight. The cross-linking treatment at the second stage was stretched 1.6 times while being treated in an aqueous solution in which boric acid and potassium iodide were dissolved at 65 ° C. The boric acid content of the aqueous solution of the second crosslinking treatment was 4.3% by weight, and the potassium iodide content was 5.0% by weight. In addition, the cleaning treatment was performed with an aqueous potassium iodide solution at 20 ° C. The potassium iodide content of the aqueous solution for the washing treatment was 2.6% by weight. Finally, the drying process was performed at 70 ° C. for 5 minutes to obtain a polarizer 1.
A TAC film manufactured by Konica Minolta Co., Ltd. (product name: KC2UA, thickness: 25 μm, corresponding to the second protective layer) and the TAC film on both surfaces of the obtained polarizer 1 through a polyvinyl alcohol adhesive. HC-TAC films (thickness: 32 μm, corresponding to the first protective layer) each having a hard coat (HC) layer formed by a hard coat treatment on one side of each of the first protective layer / polarizer A polarizing plate 1 having a configuration of 1 / second protective layer was obtained.

[Reference Example 2: Production of liquid crystal alignment solidified layer constituting first retardation layer]
10 g of a polymerizable liquid crystal exhibiting a nematic liquid crystal phase (manufactured by BASF: trade name “Pariocolor LC242”, represented by the following formula) and a photopolymerization initiator for the polymerizable liquid crystal compound (manufactured by BASF: trade name “IRGACURE 907”). 3) was dissolved in 40 g of toluene to prepare a liquid crystal composition (coating solution).

The surface of a polyethylene terephthalate (PET) film (thickness 38 μm) was rubbed with a rubbing cloth and subjected to orientation treatment. The conditions of the alignment treatment are as follows: the number of rubbing times (the number of rubbing rolls) is 1, the rubbing roll radius r is 76.89 mm, the rubbing roll rotational speed nr is 1500 rpm, the film transport speed v is 83 mm / sec, the rubbing strength RS and the pushing amount M was performed under five conditions (a) to (e) as shown in Table 1.

The direction of the orientation treatment was set to a −75 ° direction when viewed from the viewing side with respect to the direction of the absorption axis of the polarizer when being bonded to the polarizing plate. The liquid crystal coating liquid was applied to the alignment-treated surface with a bar coater, and the liquid crystal compound was aligned by heating and drying at 90 ° C. for 2 minutes. Under the conditions (a) to (c), the alignment state of the liquid crystal compound was very good. Under the conditions (d) and (e), a slight disturbance occurred in the alignment of the liquid crystal compound, but the level was not problematic for practical use. The liquid crystal layer thus formed is irradiated with 1 mJ / cm ² of light using a metal halide lamp, and the liquid crystal layer is cured to form a retardation layer (liquid crystal alignment solidified layer) 1 on the PET film. Formed. The thickness of the retardation layer 1 was 2 μm, and the in-plane retardation Re (550) was 236 nm. Furthermore, the retardation layer 1 had a refractive index distribution of nx> ny = nz.

[Reference Example 3: Production of liquid crystal alignment solidified layer constituting second retardation layer]
The surface of a polyethylene terephthalate (PET) film (thickness 38 μm) was rubbed with a rubbing cloth and subjected to orientation treatment. The direction of the alignment treatment was set to −15 ° when viewed from the viewing side with respect to the direction of the absorption axis of the polarizer when being bonded to the polarizing plate. A liquid crystal coating liquid similar to that of Reference Example 2 was applied to the alignment-treated surface, and the liquid crystal compound was aligned and cured in the same manner as in Reference Example 2 to form the retardation layer 2 on the PET film. The thickness of the retardation layer 2 was 1.2 μm, and the in-plane retardation Re (550) was 115 nm. Further, the retardation layer 2 had a refractive index distribution of nx> ny = nz.

[Reference Example 4: Production of laminated retardation film constituting first retardation layer and second retardation layer]
Kaneka's cycloolefin phase difference film A (product name: KUZ-film # 270, thickness: 33 μm, Re (550) = 270 nm) and Kaneka's cycloolefin phase difference film B (product) Name: KUZ-film # 140, thickness: 28 μm, Re (550) = 140 nm) are bonded together via an acrylic adhesive layer having a thickness of 5 μm so that the angle formed by each slow axis is 60 °. Thus, a laminated retardation film was obtained. This laminated retardation film was designated as retardation layer 3.

[Reference Example 5: Production of retardation film constituting retardation layer]
7-1. Preparation of Polycarbonate Resin Film Isosorbide (ISB) 26.2 parts by mass, 9,9- [4- (2-hydroxyethoxy) phenyl] fluorene (BHEPF) 100.5 parts by mass, 1,4-cyclohexanedimethanol (1, 4-CHDM) 10.7 parts by mass, diphenyl carbonate (DPC) 105.1 parts by mass, and cesium carbonate (0.2% by mass aqueous solution) 0.591 parts by mass as a catalyst were put in a reaction vessel, respectively, and a nitrogen atmosphere Below, as a first step of the reaction, the temperature of the heating medium in the reaction vessel was set to 150 ° C., and the raw materials were dissolved while stirring as necessary (about 15 minutes).
Next, the pressure in the reaction vessel was changed from normal pressure to 13.3 kPa, and the generated phenol was extracted out of the reaction vessel while the temperature of the heat medium in the reaction vessel was increased to 190 ° C. over 1 hour.
After holding the reaction vessel temperature at 190 ° C. for 15 minutes, as a second step, the pressure in the reaction vessel is set to 6.67 kPa, and the heat medium temperature of the reaction vessel is increased to 230 ° C. in 15 minutes. The generated phenol was extracted out of the reaction vessel. Since the stirring torque of the stirrer increased, the temperature was raised to 250 ° C. in 8 minutes, and the pressure in the reaction vessel was reduced to 0.200 kPa or less in order to remove the generated phenol. After reaching a predetermined stirring torque, the reaction was terminated, and the reaction product formed was extruded into water, and then pelletized to obtain BHEPF / ISB / 1,4-CHDM = 47.4 mol% / 37.1 mol%. /15.5 mol% polycarbonate resin was obtained.
The obtained polycarbonate resin had a glass transition temperature of 136.6 ° C. and a reduced viscosity of 0.395 dL / g.
The obtained polycarbonate resin was vacuum-dried at 80 ° C. for 5 hours, and then a single-screw extruder (made by Isuzu Chemical Industries, screw diameter 25 mm, cylinder set temperature: 220 ° C.), T-die (width 200 mm, set temperature: 220). ° C.), a chill roll (set temperature: 120 to 130 ° C.), and a film forming apparatus equipped with a winder, a 120 μm thick polycarbonate resin film was produced.

7-2. Production of Retardation Film Using a tenter stretching machine, the obtained polycarbonate resin film was horizontally stretched to obtain a retardation film having a thickness of 50 μm. At that time, the draw ratio was 250%, and the draw temperature was 137 to 139 ° C.
Re (550) of the obtained retardation film is 137 to 147 nm, Re (450) / Re (550) is 0.89, Nz coefficient is 1.21, orientation angle (slow axis) Direction) was 90 ° with respect to the longitudinal direction. This retardation film was used as the retardation layer 4.

[Reference Example 6: Production of conductive film (conductive layer with substrate)]
A polycycloolefin film (manufactured by Zeon Corporation, trade name “ZEONOR (registered trademark)”) having a thickness of 50 μm was used as the substrate. An ultraviolet curable resin composition (trade name “UNIDIC (registered trademark) RS29-120” manufactured by DIC) was applied to one surface of the base material, dried at 80 ° C. for 1 minute, then cured with ultraviolet light, and then thickened. A 1.0 μm hard coat layer was formed. Next, on the other side of the substrate, 100 parts by weight of the same UV curable resin composition as described above, and acrylic spherical particles having a mode particle diameter of 1.9 μm (trade name “MX-180TA, manufactured by Soken Chemical Co., Ltd.) “) A curable resin composition containing spherical particles containing 0.002 part by weight was applied and then cured with ultraviolet rays to form a hard coat layer having a thickness of 1.0 μm. The polycycloolefin film obtained above was put into a sputtering apparatus, and an amorphous layer of indium tin oxide having a thickness of 27 nm was formed on the surface of the hard coat layer not containing particles. Next, the polyolefin film on which the amorphous layer of indium tin oxide was formed was heat-treated in a heating oven at 130 ° C. for 90 minutes to produce a transparent conductive film having a surface resistance value of 100Ω / □. This transparent conductive film was used as a conductive layer with a substrate. The moisture permeability of the substrate according to the above (3) is 7 mg / m ² · 24 h, the dimensional change rate according to the above (4) is 0.03%, and the linear expansion coefficient according to the above (5) is 7.3 (× 10 ⁻⁶ / ° C.).

[Reference Example 7: Production of conductive film (conductive layer with substrate)]
A transparent conductive film having a surface resistance value of 100Ω / □ was prepared in the same manner as in Reference Example 6 except that a PET film having a thickness of 50 μm (trade name “Lumirror # 50” manufactured by Toray Industries, Inc.) was used as the substrate. This transparent conductive film was used as a conductive layer with a substrate. The moisture permeability of the substrate according to the above (3) is 700 mg / m ² · 24 h, the dimensional change rate according to the above (4) is 0.50%, and the linear expansion coefficient according to the above (5) is 13.0 (× 10 ⁻⁶ / ° C.).

[Reference Example 8: Production of pressure-sensitive adhesive layer]
In a reaction vessel equipped with a cooling tube, a nitrogen introduction tube, a thermometer and a stirrer, 99 parts of butyl acrylate, 1.0 part of 4-hydroxybutyl acrylate and 2,2′-azobisisobutyronitrile 0.3 Part was added with ethyl acetate. After the mixture in the reaction vessel was reacted at 60 ° C. for 4 hours under a nitrogen gas stream, ethyl acetate was added to the reaction solution, and a solution containing an acrylic polymer having a weight average molecular weight of 1,650,000 (solid content concentration of 30 %). 0.15 parts dibenzoyl peroxide (Nippon Yushi Co., Ltd .: Nyper BO-Y) and 0.1 parts trimethylolpropane xylene diisocyanate (Mitsui Takeda Chemical (100% solids content of the acrylic polymer solution)) Ltd.): Takenate D110N) and 0.2 part of a silane coupling agent (manufactured by Soken Chemical Co., Ltd .: A-100, acetoacetyl group-containing silane coupling agent) Obtained. The pressure-sensitive adhesive layer forming solution was applied to a separator made of a polyester film surface-treated with a silicone release agent, and heat-treated at 155 ° C. for 3 minutes to obtain a pressure-sensitive adhesive layer A having a thickness of 15 μm.

[Reference Example 9: Production of pressure-sensitive adhesive layer]
In a reaction vessel equipped with a cooling tube, a nitrogen introduction tube, a thermometer and a stirrer, 94.9 parts of butyl acrylate, 5 parts of acrylic acid and 0.1 part of 2-hydroxyethyl acrylate, and monomers thereof (solid Min) To 100 parts, 0.3 part of benzoyl peroxide was added together with ethyl acetate. After the mixture in the reaction vessel was reacted at 60 ° C. for 7 hours under a nitrogen gas stream, ethyl acetate was added to the reaction solution, and a solution containing an acrylic polymer having a weight average molecular weight of 2.2 million (solid content concentration of 30 % By weight). 0.6 part of trimethylolpropane tolylene diisocyanate (manufactured by Nippon Polyurethane Co., Ltd .: Coronate L) and 0.075 part of γ-glycidoxypropylmethoxysilane (Shin-Etsu) per 100 parts of the solid content of the acrylic polymer solution. Chemical Industry Co., Ltd. product: KBM-403) was blended to obtain an adhesive layer forming solution. The pressure-sensitive adhesive layer forming solution was applied to a separator made of a polyester film surface-treated with a silicone release agent, and heat-treated at 155 ° C. for 3 minutes to obtain a pressure-sensitive adhesive layer B having a thickness of 15 μm.

[Example 1]
An acrylic adhesive having a thickness of 5 μm is used so that the angle between the absorption axis of the polarizer and the slow axis of the retardation layer 1 is 15 ° between the second protective layer surface of the polarizing plate 1 and the retardation layer 1. Pasted together. Next, the PET film on which the phase difference layer 1 has been formed is peeled off, and the phase difference layer 2 is formed on the peeled surface, and the angle between the absorption axis of the polarizer and the slow axis of the phase difference layer 2 is 75 °. In this way, they were bonded together through an acrylic adhesive having a thickness of 5 μm. Furthermore, the PET film on which the retardation layer 2 was formed was peeled off to obtain a circularly polarizing plate 1 having a configuration of polarizing plate / first retardation layer / second retardation layer. The second retardation layer of the circularly polarizing plate 1 and the conductive layer of the conductive layer with a base material obtained in Reference Example 6 were bonded to each other through the pressure-sensitive adhesive layer A to obtain an optical laminate 1. The obtained optical laminated body 1 was used for evaluation of said (6). The results are shown in Table 2.

[Example 2]
A retardation layer 3 (laminated retardation film) is used instead of the retardation layers 1 and 2, and the second protective layer surface of the polarizing plate 1 and the surface of the retardation layer film A are connected to the absorption axis of the polarizer and the retardation. An acrylic adhesive having a thickness of 12 μm is used so that the angle between the slow axis of the film A is 15 ° and the angle between the absorption axis of the polarizer and the slow axis of the retardation film B is 75 °. A circularly polarizing plate 2 having a configuration of polarizing plate / first retardation layer / second retardation layer was obtained by bonding. The second retardation layer of the circularly polarizing plate 2 and the conductive layer of the conductive layer with a base material obtained in Reference Example 6 were bonded to each other through the pressure-sensitive adhesive layer A to obtain an optical laminate 2. The obtained optical laminate 2 was subjected to the evaluation of (6) above. The results are shown in Table 2.

[Comparative Example 1]
The optical laminated body 3 was obtained like Example 1 except having used the electrically conductive layer with a base material obtained in Reference Example 7. The obtained optical laminated body 3 was used for evaluation of said (6). The results are shown in Table 2.

[Comparative Example 2]
The optical laminated body 4 was obtained like Example 2 except having used the electroconductive layer with a base material obtained in Reference Example 7. The obtained optical laminated body 4 was used for evaluation of said (6). The results are shown in Table 2.

The optical layered body of the present invention is suitably used for image display devices such as liquid crystal display devices and organic EL display devices, and can be particularly suitably used as an antireflection film for organic EL display devices. Furthermore, the optical layered body of the present invention can be suitably used for an inner touch panel type input display device.

DESCRIPTION OF SYMBOLS 10 Polarizing plate 11 Polarizer 12 1st protective layer 13 2nd protective layer 20 1st phase difference layer 30 2nd phase difference layer 41 Conductive layer 42 Base material 100 Optical laminated body

Claims (7)

1. A polarizer, a polarizing plate including a protective layer on at least one side of the polarizer, a first retardation layer, a second retardation layer, a conductive layer, and a substrate laminated in close contact with the conductive layer And in this order,
   The substrate has a moisture permeability of 5 mg / m ² · 24 h to 10 mg / m ² · 24 h, a dimensional change rate of 0.3% or less, and a linear expansion coefficient of 5 (× 10 ⁻⁶ / ° C.). To 10 (× 10 ⁻⁶ / ° C.),
   Optical laminate.
2. The angle formed between the absorption axis of the polarizer and the slow axis of the first retardation layer is 10 ° to 20 °, and the angle formed between the absorption axis and the slow axis of the second retardation layer The optical laminate according to claim 1, wherein is from 65 ° to 85 °.
3. The optical laminate according to claim 1 or 2, wherein the first retardation layer and the second retardation layer are composed of a cyclic olefin-based resin film.
4. The optical laminate according to claim 3, wherein a dimensional change rate of the second retardation layer is 1% or less.
5. The optical layered body according to claim 1 or 2, wherein the first retardation layer and the second retardation layer are alignment solidified layers of a liquid crystal compound.
6. 6. The optical laminate according to claim 5, wherein a dimensional change rate of the laminate of the polarizing plate, the first retardation layer, and the second retardation layer is 1% or less.
7. An image display apparatus provided with the optical laminated body in any one of Claim 1 to 6.
   

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