Anti-reflection film and image display device using the same
Patent Information
- Authority / Receiving Office
- JP · JP
- Patent Type
- Applications
- Current Assignee / Owner
- TOPPAN TOMOEGAWA OPTICAL FILM CO LTD
- Filing Date
- 2024-03-26
- Publication Date
- 2026-05-21
AI Technical Summary
Existing anti-glare films suffer from increased haze leading to decreased panel contrast and a loss of luxurious feel when viewed from the front, and their anti-glare performance significantly deteriorates when viewed from an oblique angle.
An anti-reflection film with an optical functional layer containing ultraviolet-curable resin and spinous-shaped microparticles, where the radius of curvature of the core and protrusions satisfy specific formulas, forming fine irregularities to scatter light effectively.
The film achieves low haze and high anti-glare properties, maintaining performance when viewed from both front and oblique angles, thereby enhancing image clarity and reducing glare without compromising contrast.
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Abstract
Description
[Technical Field]
[0001] The present invention relates to an anti-reflection film and an image display device using the same. [Background technology]
[0002] When a display is used in a relatively bright location such as outdoors or under fluorescent lights, reflection of external light such as sunlight or fluorescent lights on the display can be a problem. To prevent this reflection, anti-glare films are used, which have fine irregularities on their surfaces and diffuse the reflected external light.
[0003] Antiglare films include those obtained by coating a transparent film with a transparent resin and then performing a shaping process using a shaping mold with uneven surfaces, and those obtained by coating a transparent film with a paint in which inorganic or organic transparent fine particles are dispersed in a resin binder (for the latter, see, for example, Patent Documents 1 to 3). [Prior art documents] [Patent documents]
[0004] [Patent Document 1] Patent No. 4839212 [Patent Document 2] Japanese Patent Application Laid-Open No. 2009-122490 [Patent Document 3] Japanese Patent Application Laid-Open No. 2012-220898 Summary of the Invention [Problem to be solved by the invention]
[0005] When anti-glare films are designed to have high anti-glare properties, the haze tends to increase as well, resulting in a decrease in panel contrast and a loss of the luxurious feel due to cloudiness.
[0006] Furthermore, anti-glare treatments using shaping processes and the anti-glare films described in Patent Documents 1 to 3 have the problem that, although they have high anti-glare performance when viewed from the front (in the range of 0 to 30 degrees relative to the normal to the screen), when viewed from an angle (in the range of 45 degrees or more relative to the normal to the screen), the anti-glare performance is significantly reduced compared to when viewed from the front.
[0007] Therefore, an object of the present invention is to provide an anti-reflection film that has low haze and high anti-glare properties and in which the deterioration of the anti-glare properties when viewed from an oblique angle is suppressed, and an image display device using the same. [Means for solving the problem]
[0008] The anti-reflection film of the present invention is characterized in that at least one optical functional layer is laminated on a light-transmitting substrate, and an uneven shape is formed on at least one surface of the optical functional layer, and the optical functional layer contains an ultraviolet-curable resin and spinous-shaped microparticles having a plurality of protrusions, and the radius of curvature r1 of the core of the spinous-shaped microparticles and the radius of curvature r2 of the protrusions of the spinous-shaped microparticles satisfy the following formulas (A), (B), and (C). 0.75μm≦r1≦4.0μm (A) 0.05μm≦r2≦1.0μm (B) 0.25μmm≦r1-r2 (C)
[0009] An image display device according to the present invention includes an image display panel and the above-described anti-reflection film. [Effects of the Invention]
[0010] The present invention can provide an anti-reflection film that has low haze and high anti-glare properties and in which the deterioration of the anti-glare properties when viewed from an oblique angle is suppressed, and an image display device using the same. [Brief explanation of the drawings]
[0011] [Figure 1] 1 is a cross-sectional view schematically illustrating an anti-reflection film according to an embodiment. [Figure 2] SEM image of confetti-shaped microparticles [Figure 3] Schematic diagram of confetti-shaped particles [Figure 4] Graph showing the relationship between the light receiving angle and the relative value of the amount of reflected light [Figure 5] Graph showing the relationship between the light-receiving angle and the relative value of the amount of reflected light of the anti-reflection film according to Example 1 [Figure 6] Graph showing the relationship between the light-receiving angle and the relative value of the amount of reflected light of the anti-reflection film according to Comparative Example 1 DETAILED DESCRIPTION OF THE INVENTION
[0012] FIG. 1 is a cross-sectional view schematically showing an antireflection film according to an embodiment.
[0013] The anti-reflection film 1 includes a light-transmitting substrate 2 and an anti-glare layer 3 laminated on one surface of the light-transmitting substrate 2. The anti-glare layer 3 is an optically functional layer that scatters incident light with fine irregularities formed on its surface, thereby suppressing the glare of external light. The anti-reflection film 1 including the anti-glare layer 3 is also called an AG film.
[0014] The light-transmitting substrate 2 is a film that serves as the base of the anti-reflection film 1 and is made of a material that has excellent transmittance to visible light. Materials that can be used to form the light-transmitting substrate 2 include polyolefins such as polyethylene and polypropylene, polyesters such as polyethylene terephthalate, polybutylene terephthalate, and polyethylene naphthalate, polyacrylates such as polymethyl methacrylate, polyamides such as nylon 6 and nylon 66, polyimides, polyarylates, polycarbonates, triacetyl cellulose, polyacrylates, polyvinyl alcohol, polyvinyl chloride, cycloolefin copolymers, norbornene-containing resins, polyethersulfones, and transparent resins such as polysulfones, and inorganic glass. The thickness of the light-transmitting substrate 2 is not particularly limited, but is preferably 10 to 200 μm.
[0015] The surface of the light-transmitting substrate 2 may be subjected to a surface modification treatment to improve adhesion with other layers to be laminated thereon. Examples of surface modification treatments include alkali treatment, corona treatment, plasma treatment, sputtering treatment, application of a surfactant or a silane coupling agent, and Si vapor deposition.
[0016] The antiglare layer 3 is a functional layer that forms the fine irregularities on the outermost surface of the antireflection film 1 .
[0017] The antiglare layer 3 contains an ultraviolet curable resin and confetti-shaped fine particles (filler). The antiglare layer 3 is formed by applying a coating liquid containing an ultraviolet curable compound, confetti-shaped fine particles, and a photopolymerization initiator to the light-transmitting substrate 2 and curing the coating film.
[0018] As the ultraviolet-curable compound, for example, a monofunctional, difunctional, trifunctional or higher functional (meth)acrylate monomer can be used. In this specification, "(meth)acrylate" is a general term for both acrylate and methacrylate, and "(meth)acryloyl" is a general term for both acryloyl and methacryloyl.
[0019] Examples of monofunctional (meth)acrylate compounds include 2-hydroxyethyl (meth)acrylate, 2-hydroxypropyl (meth)acrylate, 2-hydroxybutyl (meth)acrylate, n-butyl (meth)acrylate, isobutyl (meth)acrylate, t-butyl (meth)acrylate, glycidyl (meth)acrylate, acryloylmorpholine, N-vinylpyrrolidone, tetrahydrofurfuryl acrylate, cyclohexyl (meth)acrylate, 2-ethylhexyl (meth)acrylate, and isobornyl (meth)acrylate. acrylate, isodecyl (meth)acrylate, lauryl (meth)acrylate, tridecyl (meth)acrylate, cetyl (meth)acrylate, stearyl (meth)acrylate, benzyl (meth)acrylate, 2-ethoxyethyl (meth)acrylate, 3-methoxybutyl (meth)acrylate, ethyl carbitol (meth)acrylate, phosphate (meth)acrylate, ethylene oxide-modified phosphate (meth)acrylate, phenoxy (meth)acrylate, ethylene oxide-modified phenoxy (meth)acrylate, propylene oxide Oxide-modified phenoxy (meth)acrylate, nonylphenol (meth)acrylate, ethylene oxide-modified nonylphenol (meth)acrylate, propylene oxide-modified nonylphenol (meth)acrylate, methoxydiethylene glycol (meth)acrylate, methoxypolyethylene glycol (meth)acrylate, methoxypropylene glycol (meth)acrylate, 2-(meth)acryloyloxyethyl-2-hydroxypropyl phthalate, 2-hydroxy-3-phenoxypropyl (meth)acrylate, 2-(meth)acryloyloxyethyl-2-hydroxypropyl phthalate, ) acryloyloxyethyl hydrogen phthalate, 2-(meth)acryloyloxypropyl hydrogen phthalate, 2-(meth)acryloyloxypropyl hexahydrohydrogen phthalate, 2-(meth)acryloyloxypropyl tetrahydrohydrogen phthalate, dimethylaminoethyl (meth)acrylate, trifluoroethyl (meth)acrylate, tetrafluoropropyl (meth)acrylate, hexafluoropropyl (meth)acrylate, octafluoropropyl (meth)acrylate, 2-adamantane,Examples include adamantane derivative mono(meth)acrylates such as adamantyl acrylate having a monovalent mono(meth)acrylate derived from adamantanediol.
[0020] Examples of bifunctional (meth)acrylates include di(meth)acrylates such as ethylene glycol di(meth)acrylate, diethylene glycol di(meth)acrylate, butanediol di(meth)acrylate, hexanediol di(meth)acrylate, nonanediol di(meth)acrylate, ethoxylated hexanediol di(meth)acrylate, propoxylated hexanediol di(meth)acrylate, diethylene glycol di(meth)acrylate, polyethylene glycol di(meth)acrylate, tripropylene glycol di(meth)acrylate, polypropylene glycol di(meth)acrylate, neopentyl glycol di(meth)acrylate, ethoxylated neopentyl glycol di(meth)acrylate, tripropylene glycol di(meth)acrylate, and hydroxypivalic acid neopentyl glycol di(meth)acrylate.
[0021] Examples of tri- or higher functional (meth)acrylates include tri(meth)acrylates such as trimethylolpropane tri(meth)acrylate, ethoxylated trimethylolpropane tri(meth)acrylate, propoxylated trimethylolpropane tri(meth)acrylate, tris(2-hydroxyethyl)isocyanurate tri(meth)acrylate, and glycerin tri(meth)acrylate; trifunctional (meth)acrylate compounds such as pentaerythritol tri(meth)acrylate, dipentaerythritol tri(meth)acrylate, and ditrimethylolpropane tri(meth)acrylate; Examples of the polyfunctional (meth)acrylate compound include tri- or higher functional polyfunctional (meth)acrylate compounds such as pentaerythritol tetra(meth)acrylate, ditrimethylolpropane tetra(meth)acrylate, dipentaerythritol tetra(meth)acrylate, dipentaerythritol penta(meth)acrylate, ditrimethylolpropane penta(meth)acrylate, dipentaerythritol hexa(meth)acrylate, and ditrimethylolpropane hexa(meth)acrylate, as well as polyfunctional (meth)acrylate compounds in which a portion of these (meth)acrylates is substituted with an alkyl group or ε-caprolactone.
[0022] Urethane (meth)acrylates can also be used as polyfunctional monomers. Examples of urethane (meth)acrylates include those obtained by reacting a polyester polyol with an isocyanate monomer or a prepolymer, and then reacting the resulting product with a (meth)acrylate monomer having a hydroxyl group.
[0023] Examples of urethane (meth)acrylates include pentaerythritol triacrylate hexamethylene diisocyanate urethane prepolymer, dipentaerythritol pentaacrylate hexamethylene diisocyanate urethane prepolymer, pentaerythritol triacrylate toluene diisocyanate urethane prepolymer, dipentaerythritol pentaacrylate toluene diisocyanate urethane prepolymer, pentaerythritol triacrylate isophorone diisocyanate urethane prepolymer, and dipentaerythritol pentaacrylate isophorone diisocyanate urethane prepolymer.
[0024] The polyfunctional monomers may be used alone or in combination of two or more thereof. In addition, the polyfunctional monomers may be in the form of a monomer in the coating liquid, or may be in the form of a partially polymerized oligomer.
[0025] FIG. 2 is an SEM image of the confetti-shaped particles, and FIG. 3 is a schematic diagram of the confetti-shaped particles.
[0026] The confetti-shaped particles are a material that forms minute irregularities on the surface of the anti-glare layer 3, imparting the function of diffusing external light. As shown in FIG. 2, the confetti-shaped particles have a spherical core and multiple protrusions protruding from the surface of the core. The protrusions on the surface of the confetti-shaped particles have a shape that approximates a portion of a sphere, and the outer surfaces of the protrusions are approximately spherical. The confetti-shaped particles are made of resin, and examples of materials that can be used for the confetti-shaped particles include acrylic resins and polymethylsilsesquioxane (PMSQ).
[0027] Here, the radius of curvature of the core is r1, and the radius of curvature of the protrusions is r2 (see Figure 3). The radii of curvature r1 and r2 are approximate values measured assuming the core and protrusions are spheres, and specifically, they are values calculated as the radius of a circle passing through any three points on the outline of the core and protrusions that appear in an SEM image. As an example, in Figure 3, a circle passing through any three points on the outline of one of the protrusions is shown by a dashed line. The radii of curvature r1 and r2 of the spinous-shaped microparticles used in the anti-reflection film according to this embodiment satisfy the following formulas (A), (B), and (C). 0.75μm≦r1≦4.0μm (A) 0.05μm≦r2≦1.0μm (B) 0.25μmm≦r1-r2 (C)
[0028] If the radius of curvature r1 of the core is less than 0.75 μm, the haze will be small, but the antiglare properties will also be reduced. If the radius of curvature r2 of the core exceeds 4.0 μm, the antiglare properties will be high, but the haze will also be high. If the radius of curvature r1 of the core is within the range of formula (A), high antiglare properties and low haze can both be achieved. The haze of the antireflection film of the present invention should be 20% or less, and more preferably 15% or less.
[0029] If the radius of curvature r2 of the protrusions is less than 0.05 μm, the shape of the confetti-shaped particles becomes nearly spherical, resulting in reduced anti-glare properties when the anti-reflection film is viewed obliquely. If the radius of curvature r2 of the protrusions exceeds 1.0 μm, the anti-glare properties when the anti-reflection film is viewed obliquely also decrease. Furthermore, if r2 is too large, it becomes difficult to produce the confetti-shaped particles.
[0030] If the difference in the radii of curvature r1-r2 becomes too small, it becomes difficult to produce confetti-shaped particles, so the practical lower limit of r1-r2 is 0.25 or more.
[0031] Examples of photopolymerization initiators that can be used include radical polymerization initiators such as acetophenones, benzophenones, thioxanthones, benzoin, benzoin methyl ether, and acylphosphine oxides. Examples of photopolymerization initiators that can be used include diphenyl(2,4,6-trimethylbenzoyl)phosphine oxide, bis(2,4,6-trimethylbenzoyl)phenylphosphine oxide, 2,2-diethoxyacetophenone, 1-hydroxycyclohexyl phenyl ketone, 2,2-dimethoxy-phenylacetophenone, dibenzoyl, benzoin, benzoin methyl ether, benzoin ethyl ether, p-chlorobenzophenone, p-methoxybenzophenone, Michler's ketone, acetophenone, and 2-chlorothioxanthone. These initiators may be used alone or in combination.
[0032] If necessary, inorganic fine particles (inorganic nanoparticles) having an average particle size of 10 to 200 nm may be added to the composition for forming an antiglare layer.
[0033] The inorganic fine particles function as a thickener that increases the viscosity of the antiglare layer-forming composition and are a material for adjusting the sedimentation and aggregation of the confetti-shaped fine particles in the antiglare layer 3. Examples of inorganic fine particles that can be used include silica fine particles, metal oxide fine particles, and various mineral fine particles. Examples of silica fine particles that can be used include colloidal silica and silica fine particles surface-modified with a reactive functional group such as a (meth)acryloyl group. Examples of metal oxide fine particles that can be used include alumina, zinc oxide, tin oxide, antimony oxide, indium oxide, titania, and zirconia. Examples of mineral fine particles that can be used include mica, synthetic mica, vermiculite, montmorillonite, iron-montmorillonite, bentonite, beidellite, saponite, hectorite, stevensite, nontronite, magadiite, ilealite, kanemite, layered titanic acid, smectite, and synthetic smectite. The mineral fine particles may be either natural or synthetic (including substituted or derivative) materials, or a mixture of the two may be used. Among the mineral fine particles, layered organic clays are more preferred. Layered organic clays refer to swelling clays in which organic onium ions have been introduced between the layers. There are no limitations on the organic onium ions, as long as they can be organized by utilizing the cation exchange properties of the swelling clay. When layered organic clay minerals are used as the mineral fine particles, the above-mentioned synthetic smectites can be suitably used.
[0034] The antiglare layer-forming composition may also contain components for improving antifouling properties, such as an antifouling agent, a leveling agent, an oil repellent, a water repellent, or an antifingerprint agent. Fluorine-containing compounds and silicone compounds can be suitably used as these additives. Other additives, such as antistatic agents, antifoaming agents, antioxidants, ultraviolet absorbers, infrared absorbers, colorants, light stabilizers, polymerization inhibitors, and photosensitizers, may also be added as needed.
[0035] A solvent may be added to the antiglare layer-forming composition, if necessary. Examples of the solvent include alcohols such as methanol, ethanol, 1-propanol, 2-propanol, butanol, isopropyl alcohol, and isobutanol; ketones such as acetone, methyl ethyl ketone, cyclohexanone, and methyl isobutyl ketone; ketone alcohols such as diacetone alcohol; aromatic hydrocarbons such as benzene, toluene, and xylene; glycols such as ethylene glycol, propylene glycol, and hexylene glycol; glycol ethers such as ethyl cellosolve, butyl cellosolve, ethyl carbitol, butyl carbitol, diethyl cellosolve, diethyl carbitol, and propylene glycol monomethyl ether; esters such as methyl lactate, ethyl lactate, methyl acetate, ethyl acetate, butyl acetate, and amyl acetate; ethers such as dimethyl ether and diethyl ether; and N-methylpyrrolidone and dimethylformamide, which may be used alone or in combination.
[0036] Between the light-transmitting substrate 2 and the antiglare layer 3, one or more other functional layers such as a hard coat layer, a high refractive index layer, a medium refractive index layer, an antistatic layer, an electromagnetic wave blocking layer, an infrared absorbing layer, an ultraviolet absorbing layer, or a color correction layer may be laminated as necessary.
[0037] The method for applying the antiglare layer-forming composition and the low refractive index layer-forming composition is not particularly limited, and for example, they can be applied using a spin coater, a roll coater, a reverse roll coater, a gravure coater, a microgravure coater, a knife coater, a bar coater, a wire bar coater, a die coater, a dip coater, a spray coater, an applicator, or the like.
[0038] The transmitted image clarity Ic and haze Ha of the antireflection film of the present invention preferably satisfy the following formula (D): Here, the transmitted image clarity Ic is a value measured using an optical comb with a width of 0.5 mm, and the haze (total haze) Ha is a value measured in accordance with JIS K7136. (1-Ic) / Ha≧5 (D)
[0039] The value of (1-Ic) / Ha is an index showing the balance between antiglare properties and haze, and when condition (D) is satisfied, high antiglare properties and low haze can both be achieved.
[0040] Fig. 4 is a graph showing the relationship between the light-receiving angle and the relative value of the reflected light amount. The light-receiving angle shown in Fig. 4 represents the angle of reflected light other than specularly reflected light, with the angle of specularly reflected light being set as the reference angle (0°).
[0041] Let x be the maximum relative value of the reflected light intensity relative to the light intensity of incident light incident at an incident angle of 30°, and y be the maximum relative value of the reflected light intensity relative to the light intensity of incident light incident at an incident angle of 60°. Here, the relative value of reflected light intensity is the ratio of the light intensity of reflected light to the light intensity of incident light, and the maximum values x and y are the maximum values measured while changing the light-receiving angle. Also, let α be the width (1 / 10 value width) of the light-receiving angle at which the relative value of reflected light intensity is 1 / 10 or more of the maximum value x, and let β be the width (1 / 10 value width) of the light-receiving angle at which the relative value of reflected light intensity is 1 / 10 or more of the maximum value y. Figure 4 shows x, y, α, and β.
[0042] The antireflection film of the present invention preferably satisfies the following formula (E). β / α≧0.95 (E)
[0043] The value of β / α is one of the indicators of the anti-glare properties when the anti-reflection film is observed from an oblique direction. When condition (E) is satisfied, the diffusion angle of the reflected light is maintained even when the anti-reflection film is observed from an oblique direction, and the scattering method is unlikely to change even if the angle of incidence increases, resulting in good anti-glare properties when viewed from an oblique direction.
[0044] Furthermore, the antireflection film according to the present invention preferably satisfies the following (F). y / x≦3.0 (F)
[0045] The value of y / x is one of the indicators of the anti-glare properties when the anti-reflection film is observed from an oblique direction. If condition (F) is satisfied, an increase in the amount of specularly reflected light is required even when the angle of incidence increases, and the anti-glare properties when viewed from an oblique direction are good.
[0046] As described above, the anti-reflection film according to this embodiment contains confetti-shaped microparticles as a filler in the anti-glare layer. When confetti-shaped microparticles are used, incident light is likely to be multiple-scattered by the protrusions of the confetti-shaped microparticles. Although the scattering angle is small, the incident light can be scattered in complex directions in many directions, thereby achieving high anti-glare properties (low image clarity) while maintaining low haze. Furthermore, the multiple scattering of incident light by the confetti-shaped microparticles allows the incident light to be efficiently scattered even when the light is incident from an oblique direction. Because the anti-reflection film according to this embodiment can achieve both low haze and high anti-glare properties, when used in an image display device, it is possible to suppress the effects of external light glare while also suppressing a decrease in image contrast.
[0047] The anti-reflection film according to this embodiment can be used to construct an image display device by being attached to the outermost surface of an image display panel such as a liquid crystal panel or an organic EL panel. A touch panel may be provided between the anti-reflection film and the image display panel. The anti-reflection film according to this embodiment has excellent anti-glare properties when viewed from an oblique angle, and therefore has high anti-glare properties, can display vivid images, and is suitable for large displays intended to be viewed from multiple directions, such as public information displays (PIDs). [Example]
[0048] Examples of specific implementations of the present invention will be described below.
[0049] A 40 μm-thick triacetyl cellulose (TAC) film was used as the light-transmitting substrate. A composition for forming an antiglare layer was prepared by diluting with a solvent a concentration suitable for coating, containing pentaerythritol triacrylate (a UV-curable compound), a filler (spiny-like microparticles), Omnirad® 184 (a photopolymerization initiator), and an organically treated synthetic clay (an additive) in the proportions shown in Tables 1 and 2 below. The composition is in mass %. The composition for forming an antiglare layer was applied to the light-transmitting substrate so that the film thickness after curing would be approximately equal to the particle diameter of the microparticles and would be thick enough to embed the microparticles in the antiglare layer. After drying, the coating was polymerized and cured by UV irradiation to form an antiglare layer, and antireflection films according to the examples and comparative examples were obtained.
[0050] [Table 1]
[0051] [Table 2]
[0052] The radius of curvature r1 of the core and the radius of curvature r2 of the protrusions of the spinous-shaped microparticles used in Examples 1 to 5 and Comparative Examples 3 to 5 were measured as follows: An SEM image of the cross section of the anti-reflection film was obtained, and 100 cores and 100 protrusions of any spinous-shaped microparticles included in the SEM image were selected. The radii of circles passing through any three points on the outline of the core and the protrusions were measured, and the average values were taken as r1 and r2.
[0053] (Hayes) The haze was measured in accordance with JIS K 7105 using a haze meter (NDH 4000, manufactured by Nippon Denshoku Industries Co., Ltd.).
[0054] (Transmitted image clarity Ic) The transmitted image clarity was measured in accordance with JIS K 7105 using an image clarity measuring instrument (ICM-1T, manufactured by Suga Test Instruments Co., Ltd.) in transmission mode with an optical comb width of 0.5 mm.
[0055] (relative value of reflected light amount) The relative value of the reflected light amount was measured using a variable angle photometer (goniophotometer, GP-5, manufactured by Murakami Color Research Laboratory Co., Ltd.). A black acrylic plate was attached to the uncoated side of the anti-reflection film using an optical adhesive to serve as the measurement sample. In addition, as a reference, a black acrylic plate was attached to one side of a light-transmitting substrate (the same side as the uncoated side of the anti-reflection film) using an optical adhesive, and the same side as the coated side of the anti-reflection film was used as the measurement surface.
[0056] The measurement conditions for the goniophotometer were set as follows: <Measurement conditions> Measurement mode: Reflection Measurement item: Angle VS1 (light source (light beam) side aperture): 2.0 VS2 (light receiving aperture): 3.0 IA (Incident Light Angle): 30° or 60° FA (tilt angle): 0.0° Receiving angle range (RA): Specular reflection angle ±20° (when the incident angle is 30°, R1: 10°, R2: 50°; when the incident angle is 60°, R1: 40°, R2: 80°) Sensitivity check: Implemented (Start: R1, End: R2) Neutral density filter: Not used ND filter: Not used
[0057] The relative value of the reflected light amount was determined by the following method. First, using the measurement surface of the reference, the reflected light amount was measured at 0.1° intervals within the above-mentioned light-receiving angle range, and the relative value of the reflected light amount (maximum value) at the light-receiving angle at which the actual measured value of the reflected light amount was maximum was set to 100. Next, a coefficient was calculated by dividing the maximum value (=100) of the relative value of the reflected light amount of the reference by the actual measured value (maximum value) of the reflected light amount. Next, using the coated surface of the antireflection film according to each example and each comparative example, the reflected light amount was measured at 0.1° intervals within the above-mentioned light-receiving angle range, and the product of the measured reflected light amount and the coefficient determined from the reference was set to the relative value of the reflected light amount.
[0058] The relative value of the reflected light amount was calculated for each of the incident angles of 30° and 60°, and the maximum value of the relative value of the reflected light amount at an incident light angle of 30° was designated x, and the maximum value of the relative value of the reflected light amount at an incident light angle of 60° was designated y. Furthermore, on a plane with the horizontal axis representing the light-receiving angle and the vertical axis representing the relative value of the reflected light amount, the light-receiving angle and the calculated relative value of the reflected light amount were plotted on a graph, and the ranges (absolute values) of the light-receiving angle that were 1 / 10 or more of x and y were designated α and β.
[0059] (Anti-glare evaluation) A sample was prepared by laminating a black acrylic plate to the uncoated surface of the anti-reflection film of each example and comparative example using an optical pressure-sensitive adhesive. The anti-glare property of the anti-reflection film when observed from the front, with fluorescent light irradiated from the front of the anti-reflection film and a position 40 cm away from the anti-reflection film surface, was defined as "front anti-glare property." The anti-glare property of the anti-reflection film when observed from the specular reflection direction (a direction horizontal to the normal to the anti-reflection film and tilted 60 degrees toward the opposite side of the light source) when fluorescent light irradiated from a position 40 cm away from the anti-reflection film surface, with the anti-reflection film tilted 60 degrees horizontally from the normal to the anti-reflection film, was defined as "60-degree anti-glare property."
[0060] Twenty evaluators visually compared the front anti-glare properties and 60-degree anti-glare properties of the anti-reflection films and scored them according to the following criteria. <Evaluation criteria> 4 points: 60-degree anti-glare performance is equivalent to front anti-glare performance 3 points: 60-degree anti-glare performance is slightly lower than front anti-glare performance 2 points: 60-degree anti-glare performance is significantly lower than front anti-glare performance 1 point: Almost no anti-glare at 60 degrees
[0061] The average scores of the 20 panelists were classified according to the following criteria to obtain an evaluation value: Level 5 or higher on the following criteria indicates good oblique anti-glare properties. <Evaluation value> Level 6: Over 3.5 and under 4.0 Level 5: Over 3.0 and under 3.5 Level 4: Over 2.5 and under 3.0 Level 3: Over 2.0 and under 2.5 Level 2: Over 1.5 and under 2.0 Level 1: 1.0 or higher and 1.5 or lower
[0062] Table 3 also shows the shape and size of the organic filler used in the antireflection films according to each example and comparative example, as well as the evaluation values of transmitted image clarity, haze, relative reflected light amount, and oblique antiglare property.
[0063] [Table 3]
[0064] The anti-reflection films of Examples 1 to 5 had good front anti-glare properties and good 60-degree anti-glare properties while suppressing haze because the anti-glare layer contained confetti-shaped microparticles that satisfied the above conditions (A) to (C).
[0065] The anti-reflection films of Comparative Examples 1 and 2 had good front anti-glare properties, but the 60-degree anti-glare properties were significantly reduced because the particles used were spherical. Furthermore, the haze also worsened because the amount of particles added was larger than in Examples 1 to 5.
[0066] The anti-reflection film of Comparative Example 3, in which confetti-shaped fine particles were added to the anti-glare layer, did not satisfy the above condition (B), and therefore had poor 60-degree anti-glare properties and high haze.
[0067] The anti-reflection films according to Comparative Examples 4 and 5, although containing confetti-shaped fine particles in the anti-glare layer, did not satisfy the above condition (A), and therefore had poor 60-degree anti-glare properties and high haze.
[0068] 5 and 6 are graphs showing the relationship between the light-receiving angle and the relative value of the amount of reflected light for the antireflection films according to Example 1 and Comparative Example 1, respectively.
[0069] In the antireflection film of Comparative Example 1 (using spherical microparticles) shown in Figure 6, when the incident angle of incident light is 60°, the proportion of reflected light components close to specularly reflected light is higher than when the incident angle is 30°. In contrast, in the antireflection film of Example 1 (using confetti-shaped microparticles) shown in Figure 5, the amount of specularly reflected light is reduced more than in Comparative Example 1, and the reflected light is dispersed over a wider range of light-receiving angles than in Comparative Example 1. It was confirmed that the antireflection film of Example 1 can suppress specularly reflected light and exhibit high antiglare properties even when the incident angle is large, as the confetti-shaped microparticles multiple-scatter the incident light. [Industrial Applicability]
[0070] The present invention can be used as an anti-reflection film for image display devices and the like. [Explanation of symbols]
[0071] 1. Anti-reflective film 2 Translucent substrate 3 Anti-glare layer
Claims
1. An anti-reflective film having at least one optical functional layer laminated on a light-transmitting substrate, An uneven surface is formed on at least one surface of the optical functional layer, The optical functional layer contains an ultraviolet-curing resin and konpeito-shaped fine particles having multiple protrusions. An anti-reflective film characterized in that the radius of curvature r1 of the nucleus of the konpeito-shaped microparticles and the radius of curvature r2 of the protrusions of the konpeito-shaped microparticles satisfy the following formulas (A), (B), and (C). 0.75μm≦r1≦4.0μm (A) 0.05μm≦r2≦1.0μm (B) 0.25μm≦r1-r2 (C)
2. The anti-reflective film according to claim 1, characterized in that the transmitted image clarity Ic and haze Ha for a comb width of 0.5 mm satisfy the following formula (D). (100-Ic) / Ha≧5 (D)
3. The anti-reflective film according to claim 1 or 2, characterized in that when x is the maximum value of the relative amount of reflected light with respect to the amount of incident light incident at an incident angle of 30°, y is the maximum value of the relative amount of reflected light with respect to the amount of incident light incident at an incident angle of 60°, α is the width of the receiving angle in which the relative amount of reflected light is 1 / 10 or more of the maximum value x, and β is the width of the receiving angle in which the relative amount of reflected light is 1 / 10 or more of the maximum value y, the following formula (E) is satisfied. β / α≧0.95 (E)
4. The anti-reflective film according to claim 1 or 2, characterized in that when x is the maximum value of the relative amount of reflected light with respect to the amount of incident light incident at an incident angle of 30°, and y is the maximum value of the relative amount of reflected light with respect to the amount of incident light incident at an incident angle of 60°, the following equation (F) is satisfied. y / x≦3.0 (F)
5. Image display panel, An image display device comprising the anti-reflective film described in claim 1.