WO2007148544A1 - 白色反射フィルム - Google Patents
白色反射フィルム Download PDFInfo
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- WO2007148544A1 WO2007148544A1 PCT/JP2007/061596 JP2007061596W WO2007148544A1 WO 2007148544 A1 WO2007148544 A1 WO 2007148544A1 JP 2007061596 W JP2007061596 W JP 2007061596W WO 2007148544 A1 WO2007148544 A1 WO 2007148544A1
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- Prior art keywords
- coating layer
- spherical particles
- reflective film
- white
- particles
- Prior art date
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Classifications
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- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B5/00—Optical elements other than lenses
- G02B5/02—Diffusing elements; Afocal elements
- G02B5/0205—Diffusing elements; Afocal elements characterised by the diffusing properties
- G02B5/021—Diffusing elements; Afocal elements characterised by the diffusing properties the diffusion taking place at the element's surface, e.g. by means of surface roughening or microprismatic structures
- G02B5/0226—Diffusing elements; Afocal elements characterised by the diffusing properties the diffusion taking place at the element's surface, e.g. by means of surface roughening or microprismatic structures having particles on the surface
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B5/00—Optical elements other than lenses
- G02B5/02—Diffusing elements; Afocal elements
- G02B5/0273—Diffusing elements; Afocal elements characterized by the use
- G02B5/0284—Diffusing elements; Afocal elements characterized by the use used in reflection
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- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B5/00—Optical elements other than lenses
- G02B5/08—Mirrors
- G02B5/0808—Mirrors having a single reflecting layer
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- G—PHYSICS
- G02—OPTICS
- G02F—OPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
- G02F1/00—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
- G02F1/01—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour
- G02F1/13—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells
- G02F1/133—Constructional arrangements; Operation of liquid crystal cells; Circuit arrangements
- G02F1/1333—Constructional arrangements; Manufacturing methods
- G02F1/1335—Structural association of cells with optical devices, e.g. polarisers or reflectors
- G02F1/1336—Illuminating devices
- G02F1/133602—Direct backlight
- G02F1/133605—Direct backlight including specially adapted reflectors
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/24—Structurally defined web or sheet [e.g., overall dimension, etc.]
- Y10T428/24355—Continuous and nonuniform or irregular surface on layer or component [e.g., roofing, etc.]
- Y10T428/24372—Particulate matter
Definitions
- the present invention relates to a white reflective film for improving the luminance of a backlight for a liquid crystal display. More particularly, the present invention relates to a lamp reflector for an edge light type backlight for a liquid crystal display and a white reflective film used for a reflector of a direct type backlight for a liquid crystal display.
- a backlight that illuminates a liquid crystal cell is used.
- the LCD monitor uses an edge-light type backlight
- the LCD TV uses a direct-type backlight.
- a porous white film formed by bubbles is generally used (Patent Document 1).
- Patent Documents 2 and 3 a white film in which an ultraviolet absorbing layer is laminated has been proposed.
- Patent Document 4 a method of providing a light concealing layer on the film surface opposite to the light source in order to improve the luminance in the edge light system.
- Patent Document 5 a method of controlling the light diffusibility by selecting the difference in refractive index between the spherical particles and the binder and improving the front luminance by the light diffusing sheet.
- Patent Document 6 a method for improving luminance unevenness in the backlight by controlling the diffusibility of the film surface on the light source side in the reflective sheet in the direct type backlight is also disclosed (Patent Document 6).
- Patent Document 1 JP-A-8-262208
- Patent Document 2 JP 2001-166295 A
- Patent Document 3 Japanese Patent Laid-Open No. 2002-90515
- Patent Document 4 Japanese Patent Laid-Open No. 2002-333510
- Patent Document 5 Japanese Patent Laid-Open No. 2001-324608
- Patent Document 6 Japanese Unexamined Patent Application Publication No. 2005-173546 Disclosure of the invention
- the reflective properties of the reflective film often depend on the void structure inside the white film, but the improvement of the reflective properties by devising the void structure is becoming the limit.
- the present invention improves the brightness by devising the light source side surface of the white film. Specifically, by providing a specific coating layer on at least one surface of the white film, a white reflection film that improves reflection characteristics and contributes to an improvement in the brightness of the nocrite is provided.
- the present invention employs the following means in order to solve such problems. That is, a coating layer containing spherical particles is provided on at least one surface of a white film, and when the particle diameter of the spherical particles is R and the thickness of the coating layer is H, the surface area of the coating layer is 100H square (length of one side). The average number of particles satisfying R> H is 10 or more per square (100 H square).
- the present invention provides a backlight lamp reflector using the white reflective film, and a direct type backlight.
- the invention's effect [0009] According to the present invention, by using a white reflective film in which a specific coating layer is provided on at least one surface of a white film, it is possible to contribute to improving the luminance of the backlight when used in a backlight.
- FIG. 1 is an example of a schematic cross-sectional view of a white reflective film of the present invention.
- the inventors of the present application intensively studied a white reflective film that contributes to improving the luminance of the backlight by devising the light source side surface of the white film.
- a coating layer containing spherical particles was applied to at least one side of the white film, and the relationship between the coating thickness and the diameter of the spherical particles and the number of spherical particles were used under specific conditions, We have determined that the brightness when used for knocklight is improved compared to the case of a single film.
- the white reflective film of the present invention has a coating layer containing spherical particles on at least one side of the white film.
- R particle size of the spherical particles contained in the coating layer
- H thickness of the coating layer
- R> H is about 100H square of the coating layer surface area (a square with a side length of 100H).
- the average number of spherical particles to be filled must be 10 or more. If the average number is less than 10, the brightness enhancement effect cannot be obtained when the white film of the present invention is incorporated in a backlight.
- the average number is preferably 50 or more, more preferably 100 or more, and particularly preferably 150 or more.
- the average number of spherical particles satisfying> H is preferably 3 or more.
- the average number is more preferably 5 or more, particularly preferably 10 or more.
- the "spherical" of the spherical particles according to the present invention does not necessarily mean only a true sphere.
- the cross-sectional shape of the particle is a circle, ellipse, almost circle, almost ellipse, etc. Means.
- particle diameter R of spherical particles “thickness H of coating layer”, and “average number of spherical particles satisfying R> H” are determined as follows.
- the white reflective film of the present invention is cut in a direction perpendicular to the film plane at a knife inclination angle of 3 ° using a rotary microtome manufactured by Nippon Microtome Research Co., Ltd.
- the obtained film cross section is observed using a scanning electron microscope ABT-32 manufactured by Topcon Corporation.
- the part of the coating layer that is not the part where the spherical particles are visible on the surface of the coating layer is the part that is the binder resin that forms the coating layer. Measure the thickness of the five coating layers and calculate the average value of the coating layer. The thickness is H.
- the surface of the coating layer is observed with an optical microscope OPTIPHOTO 200 made by Konica, and a range of 100H square (vertical: 100H, horizontal: 100H square) is arbitrarily selected at five locations.
- the spherical particles present in this 100H square range are taken out and observed with an optical microscope, and the longest diameter L and shortest diameter S of the spherical particles are measured.
- the spherical particles according to the present invention preferably have a refractive index difference of less than 0.30 with respect to the refractive index of the binder resin in the coating layer.
- the “refractive index difference” is the absolute value of the difference between the refractive index of the spherical particles and the refractive index of the binder resin. If the refractive index difference is 0.30 or more In some cases, when the white reflective film of the present invention is incorporated into a backlight, the brightness enhancement effect may not be obtained.
- the refractive index difference is then preferably less than 0.10, more preferably less than 0.05, and particularly preferably less than 0.03. Most preferably, there is no refractive index difference, that is, a refractive index difference of 0.00.
- the type of spherical particles according to the present invention is not particularly limited, and any organic or inorganic system can be used.
- organic spherical particles acrylic resin particles, silicone resin particles, nylon resin particles, styrene resin particles, polyethylene resin particles, benzoguanamine resin particles, urethane resin particles, and the like can be used.
- inorganic spherical particles silica, aluminum hydroxide, aluminum oxide, zinc oxide, barium sulfide, magnesium silicate, or a mixture thereof can be used.
- the white reflective film of the present invention may deteriorate spherical particles due to light emitted from a lamp such as a cold-cathode tube during use as a backlight, particularly ultraviolet rays (for example, an optical material such as yellowing). Degradation or degradation degradation that lowers the molecular weight), aliphatic organic spherical particles that do not contain aromatic compounds are preferred, and inorganic spherical particles are more preferred.
- the binder resin for the coating layer when a binder resin made of a copolymer of an acrylic monomer and an ultraviolet absorber, which will be described later, is used as the binder resin for the coating layer, the relationship between the refractive index difference between the binder resin and the spherical particles, the particle dispersibility, In view of coating properties, it is preferable to use silicon oxide, acrylic resin particles, or silicone resin particles, more preferably acrylic resin particles.
- the content of the spherical particles in the coating layer according to the present invention is not particularly limited as long as an improvement in luminance is obtained, and is uniquely limited because it depends on the particle type, dispersibility in the coating liquid, and the like. Although it cannot be determined, it is preferably 20% by weight or more based on the entire coating layer, and more preferably 30% by weight or more. If it is less than 20% by weight, the brightness enhancement effect may not be obtained.
- the upper limit is not particularly limited, but if it exceeds 300% by weight, the coatability may be inferior, so 300% by weight or less is preferable.
- the ratio S / L of the shortest diameter S to the longest diameter L measured by the above method is preferably 0.7 or more, more preferably 0.8 or more, particularly preferably 0. 9 or more. If it is less than 0.7, the brightness enhancement effect may not be obtained.
- the coefficient of variation CV according to the present invention is a value obtained by dividing the standard deviation of the volume particle diameter of the spherical particles by the average volume particle diameter.
- the “volume particle diameter of a spherical particle” is the diameter of a true sphere having the same volume as the spherical particle.
- the “average volume particle diameter” is an average value of the volume particle diameter of the corresponding spherical particle group. This coefficient of variation CV is measured by the method described in the examples described later.
- the spherical particles according to the present invention preferably have a coefficient of variation CV of 30% or less.
- the coefficient of variation CV is greater than 30%, the uniformity of the particles is poor, the light diffusibility becomes strong, and the brightness enhancement effect may be poor.
- the coefficient of variation CV is then preferably 20% or less, more preferably 15% or less, particularly preferably 10% or less. Most preferably, all spherical particles have the same volume particle diameter, that is, the coefficient of variation CV is 0%.
- the thickness H of the coating layer useful for the present invention is not particularly limited, but is preferably 0.5 to 15 ⁇ m, more preferably 1 to 10 zm, and particularly preferably 1 to 5 zm. If the thickness H is less than 0.5 ⁇ m, the light resistance of the coating layer may be insufficient. On the other hand, if the thickness H exceeds 15 ⁇ , the luminance may decrease, which is not preferable from the viewpoint of economy.
- the white film of the base material that is useful in the present invention is better if the visible light reflectance is high.
- a white film containing bubbles inside is used.
- these white films include, but are not limited to, porous unstretched or biaxially stretched polypropylene films, porous unstretched or stretched polyethylene terephthalate films.
- porous unstretched or biaxially stretched polypropylene films porous unstretched or stretched polyethylene terephthalate films.
- porous white biaxially stretched polyethylene terephthalate film disclosed in JP-A-2002-90515 is particularly preferred as the white film according to the present invention for the reasons described above.
- the white reflective film of the present invention may deteriorate the white film of the substrate due to light emitted from a lamp such as a cold cathode tube during use as a backlight, particularly ultraviolet rays (for example, yellowing, etc.). It is preferable to contain an ultraviolet absorber and Z or a light stabilizer in the binder resin that forms the coating layer provided on one side of the white film of the base material). ,.
- ultraviolet absorbers and light stabilizers contained in the coating layer are roughly classified into inorganic types and organic types.
- titanium oxide, zinc oxide, cerium oxide, and the like are generally known. Of these, zinc oxide is the most preferred because of its economic efficiency, UV absorption, and photocatalytic activity.
- zinc oxide FINEX — 25LP, FINEX-50LP (manufactured by Sakai Chemical Industry Co., Ltd.), Maxlite (registered trademark) ZS-032-D (manufactured by Showa Denko Co., Ltd.), etc. can be used.
- these inorganic ultraviolet absorbers are solid particles, they are generally used in combination with a binder resin that is weak in coating strength and adhesion to a substrate.
- the binder resin is not particularly limited as long as it is not deteriorated by light emitted from a lamp such as a cold cathode tube, particularly ultraviolet rays, but an aliphatic resin containing no aromatic compound is preferred.
- the white film used as the base material is a polyester film, a polyester resin is most preferable in order to provide sufficient adhesion.
- UV absorbing paint Sumise Fine (registered trademark) Z R-133 (manufactured by Sumitomo Osaka Cement Co., Ltd.) can be used as a commercial paint in which zinc oxide and a polyester resin composition are dispersed.
- organic ultraviolet absorbers examples include benzotriazole and benzophenone. Since these ultraviolet absorbers only absorb ultraviolet rays and cannot capture organic radicals generated by ultraviolet irradiation, the white film as a base material may be deteriorated in a chain by these radicals. . In order to capture these radicals and the like, a light stabilizer is preferably used in combination, and a hindered amine compound is used.
- the spherical particles according to the present invention preferably contain an ultraviolet absorber and / or a light stabilizer in the spherical particles, like the binder resin.
- the method of inclusion include a method of adding an ultraviolet absorber and Z or a light stabilizer to spherical particles, and an ultraviolet absorber having a reactive double bond when producing a resin that forms spherical particles. And / or a method in which a light stabilizer is chemically bonded to a resin by copolymerization. In view of the low bleed out of UV absorbers and light stabilizers from spherical particles, it is preferable to fix UV absorbers and / or light stabilizers by chemical bonds, as in the latter case.
- the white reflective film of the present invention preferably has an average reflectance of 85% or more at a wavelength of 400 to 700 nm measured from the surface provided with the coating layer, more preferably 87% or more, and particularly preferably. Is over 90%. If the average reflectance is less than 85%, the brightness may be insufficient depending on the liquid crystal display used. In addition, when the coating layer is provided on both surfaces of the white film, the average reflectance measured from any coating layer may be 85% or more.
- the coating solution can be applied by any method.
- methods such as gravure coating, roll coating, spin coating, reverse coating, bar coating, screen coating, blade coating, air knife coating, and date coating can be used.
- the coating liquid for forming the coating layer may be applied at the time of producing the white film of the substrate (in-line coating), or may be applied on the white film after completion of crystal orientation (off-line coating).
- the white reflective film of the present invention thus obtained can improve the luminance of the liquid crystal backlight, and according to a more preferred embodiment, the reflectance is reduced little even when used for a long time. . Therefore, the white reflective film of the present invention is suitable as a reflector for an edge light type backlight for liquid crystal displays and a reflector for a direct type backlight. You can power to use. In addition, it can be suitably used as a reflection plate for various surface light sources and a sealing film for solar cell modules that require reflection characteristics.
- the binder resin was extracted from the coating layer of the sample using an organic solvent, the organic solvent was distilled off, and the measurement was performed with respect to light having a wavelength of 589.3 nm at 20 ° C by an ellipsometry method.
- the value obtained here is defined as “the refractive index of the binder resin”.
- the coating layer of the sample was immersed in an organic solvent, and the coating layer was peeled and collected, and then the spherical particles were dropped from the coating layer by crimping and sliding on a slide glass.
- the spherical particles obtained here were confirmed to be invisible by the Becke line detection method at a temperature where the refractive index of each liquid organic compound was known.
- the refractive index of the liquid organic compound used at this time is defined as “the refractive index of the spherical particles”.
- Coulter Multisizer III (Beckman's) is used as a particle size distribution measurement device using the pore electrical resistance method. Coulter Co., Ltd.) was used. The number and volume of the particles were measured by measuring the electric resistance of the electrolyte corresponding to the volume of the particles as they pass through the pores. First, a small amount of sample was dispersed in a thin aqueous surfactant solution. Next, while observing the display on the monitor, it was added to the container of the specified electrolyte only in such an amount that the passing rate of the aperture (the pore in the detection portion) was 10-20%.
- the volume particle size was continuously measured until the number of passing particles reached 100,000, and was automatically calculated, and the average volume particle size, the standard deviation of the volume particle size, and the coefficient of variation CV were obtained.
- the value of the coefficient of variation CV can be obtained from the following formula.
- Spherical particle content spherical particle weight A (g) / 0.05 (g) X 100.
- Spectral photometer U_ 3410 (Hitachi, Ltd.) with ⁇ 60 integrating sphere 130_0632 (Hitachi, Ltd.) and 10 ° C inclined spacer, average value of reflectance at intervals of 10 nm at 400_700 nm was calculated. Part number 210-0740 manufactured by Hitachi Sokki Service Co., Ltd. was used for the standard white plate. The average value was calculated for the three samples, and this was taken as the average reflectance.
- An ultraviolet ray deterioration acceleration tester iSuper UV Tester SUV-W131 (manufactured by Iwasaki Electric Co., Ltd.) was used for forced ultraviolet irradiation test under the following conditions, and then the average reflectance was determined. The average value was calculated for the three samples, and this was used as the average reflectance after the durability test.
- Illuminance 100 mW / cm 2 , Temperature: 60 ° C, Relative humidity: 50% RH, Irradiation time: 72 hours.
- Model 1 Diffusion plate RM803 (Sumitomo Chemical Co., Ltd., thickness 2 mm) / Diffusion sheet GM3 (Kimoto Co., Ltd., thickness 100 / im) 2 sheets
- Model 2 Diffusion plate RM803 (Sumitomo Chemical Co., Ltd., thickness 2 mm) / Diffusion sheet GM3 (Kimoto Co., Ltd., thickness 100 ⁇ m) Z prism sheet BEF-II (3M, 130 ⁇ m thickness) / Polarized light separation sheet DBEF (3M, thickness 400 ⁇ m)
- the cold cathode ray tube lamp was turned on for 60 minutes to stabilize the light source, and the luminance (cd / m 2 ) was measured using a color luminance meter BM_7fast (manufactured by Topcon Corporation). The average value was calculated for the three samples, and this was used as the average luminance.
- Example 1 Hals Hybrid (registered trademark) UV-G13 (acrylic copolymer, 40% concentration solution, refractive index 1 ⁇ 49, manufactured by Nippon Shokubai Co., Ltd.): 10.0 g, toluene: 13.2 g, oxidized as spherical particles Key particles (Quartron (registered trademark) SP series, SP-3C, refractive index 1.47, coefficient of variation CV12%, manufactured by Fuso Chemical Industry Co., Ltd.): 1. Og was added with stirring to make a coating solution .
- Hals Hybrid (registered trademark) UV-G13 (acrylic copolymer, 40% concentration solution, refractive index 1.49, manufactured by Nippon Shokubai Co., Ltd.): 10.0 g, toluene: 19.2 g, oxidized as spherical particles Key particle (Quatron (registered trademark) SP series, SP-3C, refractive index 1.47, coefficient of variation CV12%, manufactured by Fuso Chemical Industry Co., Ltd.): 1. 7 g was added with stirring to prepare a coating solution.
- Hals Hybrid (registered trademark) UV-G13 (acrylic copolymer, 40% concentration solution, refractive index 1 ⁇ 49, manufactured by Nippon Shokubai Co., Ltd.): 10.0 g, toluene: 29.2 g, oxidized as spherical particles Key particles (Quatron (registered trademark) SP series, SP-3C, refractive index 1.47, coefficient of variation CV12%, manufactured by Fuso Chemical Industry Co., Ltd.): 4.0 g are added with stirring to make a coating solution. It was.
- Hals Hybrid (registered trademark) UV-G13 (acrylic copolymer, 40% concentration solution) , Refractive index 1 ⁇ 49, manufactured by Nippon Shokubai Co., Ltd.): 10.0 g, toluene: 29.2 g, polystyrene particles as spherical particles (Techpolymer (registered trademark) SBX-8, manufactured by Sekisui Plastics Co., Ltd.) Refractive index 1.59, coefficient of variation CV37%): 4.0 g was added while stirring to make a coating solution.
- Hals Hybrid (registered trademark) UV-G13 (acrylic copolymer, 40% concentration solution, refractive index 1.49, manufactured by Nippon Shokubai Co., Ltd.): 10.0 g, toluene: 29.2 g, Atari as spherical particles Nore particles (Techpolymer (registered trademark) MB30X_8 manufactured by Sekisui Plastics Co., Ltd., refractive index 1.49, coefficient of variation CV44%): 4.0 g were added with stirring to prepare a coating solution.
- Hals Hybrid (registered trademark) UV-G13 (acrylic copolymer, 40% concentration solution, refractive index 1 ⁇ 49, manufactured by Nippon Shokubai Co., Ltd.): 10 ⁇ 0 g, ethyl acetate: 8.6 g, as spherical particles
- Acrylic particles (TECHPOLYMER (registered trademark) SSX series, SSX-105, manufactured by Sekisui Plastics Co., Ltd.), refractive index 1.49, average particle size 5.0 ⁇ m, coefficient of variation CV9%): Stirring 0.08 g It added, stirring, and made the coating liquid.
- Limirror registered trademark
- E6SL manufactured by Toray Industries, Inc.
- Hals Hybrid (registered trademark) UV-G13 (acrylic copolymer, 40% concentration solution) , Refractive index 1 ⁇ 49, manufactured by Nippon Shokubai Co., Ltd.): 10 ⁇ 0g, ethyl acetate: 7.3g, acrylic particles as spherical particles (TECHPOLYMER (registered trademark) SSX series, manufactured by Sekisui Plastics Co., Ltd.), XX — 16FP, refractive index 1.49, average particle size 10.0 ⁇ m, coefficient of variation CV9%): 0.44g was added with stirring to make a coating solution.
- the white reflective film of the present invention was obtained.
- Hals Hybrid (registered trademark) UV-G13 (acrylic copolymer, 40% concentration solution, refractive index 1.49, manufactured by Nippon Shokubai Co., Ltd.): 10.0 g, ethyl acetate: 11.9 g, as spherical particles Acrylic particles (TECHPOLYMER (registered trademark) SSX series, SSX-105, refractive index 1.49, average particle size 5.0 ⁇ m, coefficient of variation CV9%, manufactured by Sekisui Plastics Co., Ltd.): 1.0 g It was added with stirring to make a coating solution.
- the white reflective film of the present invention was obtained.
- Hals Hybrid (registered trademark) UV-G13 (acrylic copolymer, 40% concentration solution, refractive index 1 ⁇ 49, manufactured by Nippon Shokubai Co., Ltd.): 1 ⁇ 0g, ethyl acetate: 1 ⁇ 9g, as spherical particles
- Acrylic particles (TECHPOLYMER (registered trademark) MBX series, XX—09FP, refractive index 1.49, average particle size 5.0 ⁇ m, coefficient of variation CV27. / 0 ) manufactured by Sekisui Plastics Co., Ltd .: 1.0 g With stirring, the mixture was added to make a coating solution.
- a white film made of 250-am porous biaxially stretched polyethylene terephthalate (Lumirror (registered trademark) E6SL manufactured by Toray Industries, Inc.) is applied with this coating solution using Metabar # 12 on one side, and the drying conditions are 120 ° dried at C, 1 minute, provided a coating layer having a dry weight 3. 5gZm 2. In this way, the white reflective finalem of the present invention was obtained.
- Limirror registered trademark
- E6SL manufactured by Toray Industries, Inc.
- the mixture was stirred for 3 minutes at 9000 rpm using a homomixer to disperse the polymerizable compound in water. Next, this dispersion was heated to 75 ° C. for 2 hours and kept at this temperature for reaction, and further heated to 90 ° C. for 3 hours.
- the dispersion was cooled to room temperature, and this dispersion was filtered using a mesh filter having an opening of 40 ⁇ m to remove aggregates and the like.
- the resulting dispersion had no aggregates and the filterability of this dispersion was very good.
- an average particle diameter of the resin particles dispersed in the filtered dispersion was 6. 4 beta m, the resin particles were spherical.
- the resin particle dispersion is washed according to a conventional method, and then filtered to separate the resin particles and the dispersion medium.
- the separated resin particles are dried, and then subjected to classification to obtain spherical particles A (coefficient of variation). CV15%) was obtained.
- Hals Hybrid (registered trademark) UV-G13 (acrylic copolymer, 40% concentration solution, refractive index 1.49, manufactured by Nippon Shokubai Co., Ltd.): 10.0 g, ethyl acetate: 11.9 g, spherical particles A (Refractive index 1.49, average particle size 6.4 xm, coefficient of variation CV15%): 1.
- a coating solution was prepared by adding Og with stirring.
- Spherical particles were silicone particles (GE Toshiba Silicones Co., Ltd. Tospearl (registered trademark), Tospar 145, refractive index 1.42, number average particle size 4.5 / im, coefficient of variation CV12%): 1. Og Except for this, it was prepared in the same manner as in Example 9, and a coating layer was provided. Thus, the white reflective film of the present invention was obtained.
- a white film (Lumirror (registered trademark) E6SL, manufactured by Toray Industries, Inc.) made of 250 ⁇ m porous biaxially stretched polyethylene terephthalate was used as a white reflective film without providing a coating layer.
- Hals Hybrid (registered trademark) UV-G13 (acrylic copolymer, 40% concentration solution, refractive index 1.49, manufactured by Nippon Shokubai Co., Ltd.): 10.0 g, toluene: 8.4 g, oxidized as spherical particles Key particles (Quatron (registered trademark) SP series, Fuso Chemical Industry Co., Ltd., SP-3C, refractive index 1.45, coefficient of variation CV12%): 0.04g was added with stirring to add the coating solution. Had made.
- Hals Hybrid (registered trademark) UV-G13 (acrylic copolymer, 40% concentration solution, refractive index 1 ⁇ 49, manufactured by Nippon Shokubai Co., Ltd.): 10 ⁇ 0g, toluene: 29.2g, silica powder as particles
- the powder (Fuji Silysia Chemical Co., Ltd. Silo Hovic (registered trademark) 100, refractive index 1.47, coefficient of variation CV39%): 4.0 g was added while stirring to prepare a coating solution.
- Example 3 In Examples using spherical silica particles:! To 3, the average number of particles satisfying R> H was 10 or more per surface area of 100H square of the coating layer, and the luminance was improved. Among them, Example 3 having a high particle content had the highest luminance.
- Example 4 using polystyrene particles, the average reflectance after the durability test decreased, It was.
- Examples 5 to 9 using spherical acrylic particles the average number of particles satisfying R> H was 10 or more per 100 H square of the surface area of the coating layer, and all showed improvement in luminance.
- Examples 8 and 9 having a coefficient of variation of 30% or less and a particle content of 20% by weight or more showed a significant improvement in luminance.
- Examples 6 and 7 having a particle content of less than 20% by weight showed little improvement in luminance.
- Example 10 in which the spherical acrylic particles contain an ultraviolet absorber and Z or a light stabilizer, the luminance is notably improved, and the reflectance is not lowered after the durability test, and the light resistance is good. there were.
- Example 11 using silicone particles, the average number of particles satisfying R> H was 10 or more per 100 H square surface area of the coating layer, and the luminance was improved. In any of Comparative Examples 1 to 3, the force at which particles satisfying R> H existed per surface area of 100H square of the coating layer, the number thereof was less than 10, and no improvement in luminance was observed.
- the white reflective film of the present invention can be suitably used as a reflector for an edge light type backlight for liquid crystal displays and a reflector for a direct type backlight.
- it can be suitably used as a reflection plate for various surface light sources and a sealing film for solar cell modules that require reflection characteristics.
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- Optics & Photonics (AREA)
- Nonlinear Science (AREA)
- Mathematical Physics (AREA)
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- Crystallography & Structural Chemistry (AREA)
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Abstract
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Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020137028649A KR101474890B1 (ko) | 2006-06-23 | 2007-06-08 | 백색 반사 필름 |
US12/305,670 US9046638B2 (en) | 2006-06-23 | 2007-06-08 | White reflection film |
KR1020087030283A KR101347143B1 (ko) | 2006-06-23 | 2007-06-08 | 백색 반사 필름 |
EP07767064A EP2034236A4 (en) | 2006-06-23 | 2007-06-08 | WHITE REFEXION FILM |
JP2007531505A JP5326277B2 (ja) | 2006-06-23 | 2007-06-08 | 白色反射フィルム |
CN2007800236455A CN101484746B (zh) | 2006-06-23 | 2007-06-08 | 白色反射膜 |
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JP2006173537 | 2006-06-23 | ||
JP2006-173537 | 2006-06-23 |
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US (1) | US9046638B2 (ja) |
EP (2) | EP2034236A4 (ja) |
JP (3) | JP5326277B2 (ja) |
KR (2) | KR101347143B1 (ja) |
CN (1) | CN101484746B (ja) |
TW (2) | TWI421443B (ja) |
WO (1) | WO2007148544A1 (ja) |
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JP2009020502A (ja) * | 2007-06-12 | 2009-01-29 | Toray Ind Inc | 白色反射フィルム |
JP2009223312A (ja) * | 2008-02-29 | 2009-10-01 | Eternal Chemical Co Ltd | ブライトネスを増進させた反射性フィルム |
CN102124380A (zh) * | 2008-08-13 | 2011-07-13 | 帝人杜邦薄膜日本有限公司 | 照明装置用反射膜 |
JP2010044238A (ja) * | 2008-08-13 | 2010-02-25 | Teijin Dupont Films Japan Ltd | 液晶表示装置用反射フィルム |
JP2010066758A (ja) * | 2008-08-13 | 2010-03-25 | Teijin Dupont Films Japan Ltd | 液晶表示装置用反射フィルム |
JP2010066759A (ja) * | 2008-08-14 | 2010-03-25 | Teijin Dupont Films Japan Ltd | 液晶表示装置用反射フィルム |
JP2010066760A (ja) * | 2008-08-14 | 2010-03-25 | Teijin Dupont Films Japan Ltd | 液晶表示装置用反射フィルム |
JP2010085843A (ja) * | 2008-10-01 | 2010-04-15 | Teijin Dupont Films Japan Ltd | 液晶表示装置用反射フィルム |
JP2010102071A (ja) * | 2008-10-23 | 2010-05-06 | Toray Ind Inc | 白色反射フィルム |
JP2010113115A (ja) * | 2008-11-06 | 2010-05-20 | Toray Ind Inc | 白色反射フィルム |
JP2010164689A (ja) * | 2009-01-14 | 2010-07-29 | Teijin Dupont Films Japan Ltd | 液晶表示装置用反射フィルム |
JP2016040605A (ja) * | 2009-10-24 | 2016-03-24 | スリーエム イノベイティブ プロパティズ カンパニー | 高い軸外反射率を有する浸漬した反射偏光子 |
JP2012108190A (ja) * | 2010-11-15 | 2012-06-07 | Teijin Dupont Films Japan Ltd | 反射フィルム |
JP2012159610A (ja) * | 2011-01-31 | 2012-08-23 | Teijin Dupont Films Japan Ltd | 反射フィルム |
JP2014127335A (ja) * | 2012-12-26 | 2014-07-07 | Sumitomo Chemical Co Ltd | 面光源装置 |
JPWO2014196534A1 (ja) * | 2013-06-07 | 2017-02-23 | 東レ株式会社 | 光反射フィルムおよびエッジライト型バックライト |
JP2014052636A (ja) * | 2013-09-10 | 2014-03-20 | Teijin Dupont Films Japan Ltd | 液晶表示装置用反射フィルム |
JP2014052644A (ja) * | 2013-10-07 | 2014-03-20 | Teijin Dupont Films Japan Ltd | 液晶表示装置用反射フィルム |
JP2016083806A (ja) * | 2014-10-24 | 2016-05-19 | 株式会社大和 | エネルギー減衰性内外装材 |
Also Published As
Publication number | Publication date |
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KR20130133066A (ko) | 2013-12-05 |
JP5790796B2 (ja) | 2015-10-07 |
TW201413172A (zh) | 2014-04-01 |
TWI421443B (zh) | 2014-01-01 |
US20100189959A1 (en) | 2010-07-29 |
CN101484746A (zh) | 2009-07-15 |
JP5505537B2 (ja) | 2014-05-28 |
EP2447602A1 (en) | 2012-05-02 |
KR20090024697A (ko) | 2009-03-09 |
KR101347143B1 (ko) | 2014-01-03 |
EP2447602B1 (en) | 2015-05-27 |
JP5326277B2 (ja) | 2013-10-30 |
KR101474890B1 (ko) | 2014-12-19 |
JP2013210639A (ja) | 2013-10-10 |
US9046638B2 (en) | 2015-06-02 |
EP2034236A1 (en) | 2009-03-11 |
JP2014095917A (ja) | 2014-05-22 |
TW200809137A (en) | 2008-02-16 |
JPWO2007148544A1 (ja) | 2009-11-19 |
EP2034236A4 (en) | 2009-12-09 |
TWI515393B (zh) | 2016-01-01 |
CN101484746B (zh) | 2013-06-12 |
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