WO2011118305A1 - White polyester film, light-reflective plate using the same, and liquid-crystal display backlight using the same - Google Patents
White polyester film, light-reflective plate using the same, and liquid-crystal display backlight using the same Download PDFInfo
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- WO2011118305A1 WO2011118305A1 PCT/JP2011/053633 JP2011053633W WO2011118305A1 WO 2011118305 A1 WO2011118305 A1 WO 2011118305A1 JP 2011053633 W JP2011053633 W JP 2011053633W WO 2011118305 A1 WO2011118305 A1 WO 2011118305A1
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- layer
- polyester film
- white polyester
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- film
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- 229920006267 polyester film Polymers 0.000 title claims abstract description 65
- 239000004973 liquid crystal related substance Substances 0.000 title claims abstract description 23
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 claims abstract description 62
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N titanium dioxide Inorganic materials O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims abstract description 61
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 60
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 claims abstract description 34
- 239000000377 silicon dioxide Substances 0.000 claims abstract description 30
- 235000012239 silicon dioxide Nutrition 0.000 claims abstract description 30
- 229920000728 polyester Polymers 0.000 claims abstract description 22
- 239000002245 particle Substances 0.000 claims description 38
- 239000010954 inorganic particle Substances 0.000 claims description 15
- 229920000642 polymer Polymers 0.000 claims description 9
- 230000006750 UV protection Effects 0.000 abstract description 7
- 239000010410 layer Substances 0.000 description 111
- -1 polyethylene terephthalate Polymers 0.000 description 24
- 229920000139 polyethylene terephthalate Polymers 0.000 description 20
- 239000005020 polyethylene terephthalate Substances 0.000 description 20
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 13
- 238000000034 method Methods 0.000 description 13
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- YIMQCDZDWXUDCA-UHFFFAOYSA-N [4-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1CCC(CO)CC1 YIMQCDZDWXUDCA-UHFFFAOYSA-N 0.000 description 4
- 230000005484 gravity Effects 0.000 description 4
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 4
- 229920001707 polybutylene terephthalate Polymers 0.000 description 4
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- 238000004383 yellowing Methods 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- 239000002202 Polyethylene glycol Substances 0.000 description 3
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- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 3
- 238000005286 illumination Methods 0.000 description 3
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- BJZYYSAMLOBSDY-QMMMGPOBSA-N (2s)-2-butoxybutan-1-ol Chemical compound CCCCO[C@@H](CC)CO BJZYYSAMLOBSDY-QMMMGPOBSA-N 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- 239000006096 absorbing agent Substances 0.000 description 2
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- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 2
- WSQZNZLOZXSBHA-UHFFFAOYSA-N 3,8-dioxabicyclo[8.2.2]tetradeca-1(12),10,13-triene-2,9-dione Chemical compound O=C1OCCCCOC(=O)C2=CC=C1C=C2 WSQZNZLOZXSBHA-UHFFFAOYSA-N 0.000 description 1
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- GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
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- JFNLZVQOOSMTJK-KNVOCYPGSA-N norbornene Chemical compound C1[C@@H]2CC[C@H]1C=C2 JFNLZVQOOSMTJK-KNVOCYPGSA-N 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 238000001579 optical reflectometry Methods 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
- 229920003207 poly(ethylene-2,6-naphthalate) Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
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- 239000002344 surface layer Substances 0.000 description 1
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- 229910000349 titanium oxysulfate Inorganic materials 0.000 description 1
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Images
Classifications
-
- 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
- G02B5/0236—Diffusing elements; Afocal elements characterised by the diffusing properties the diffusion taking place within the volume of the element
- G02B5/0242—Diffusing elements; Afocal elements characterised by the diffusing properties the diffusion taking place within the volume of the element by means of dispersed particles
-
- 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
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B5/00—Optical elements other than lenses
- G02B5/08—Mirrors
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B6/00—Light guides; Structural details of arrangements comprising light guides and other optical elements, e.g. couplings
- G02B6/0001—Light guides; Structural details of arrangements comprising light guides and other optical elements, e.g. couplings specially adapted for lighting devices or systems
- G02B6/0011—Light guides; Structural details of arrangements comprising light guides and other optical elements, e.g. couplings specially adapted for lighting devices or systems the light guides being planar or of plate-like form
- G02B6/0033—Means for improving the coupling-out of light from the light guide
- G02B6/005—Means for improving the coupling-out of light from the light guide provided by one optical element, or plurality thereof, placed on the light output side of the light guide
- G02B6/0053—Prismatic sheet or layer; Brightness enhancement element, sheet or layer
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B6/00—Light guides; Structural details of arrangements comprising light guides and other optical elements, e.g. couplings
- G02B6/0001—Light guides; Structural details of arrangements comprising light guides and other optical elements, e.g. couplings specially adapted for lighting devices or systems
- G02B6/0011—Light guides; Structural details of arrangements comprising light guides and other optical elements, e.g. couplings specially adapted for lighting devices or systems the light guides being planar or of plate-like form
- G02B6/0033—Means for improving the coupling-out of light from the light guide
- G02B6/005—Means for improving the coupling-out of light from the light guide provided by one optical element, or plurality thereof, placed on the light output side of the light guide
- G02B6/0055—Reflecting element, sheet or layer
-
- 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
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L31/00—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
- H01L31/04—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof adapted as photovoltaic [PV] conversion devices
- H01L31/042—PV modules or arrays of single PV cells
- H01L31/048—Encapsulation of modules
- H01L31/049—Protective back sheets
-
- 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E10/00—Energy generation through renewable energy sources
- Y02E10/50—Photovoltaic [PV] energy
Definitions
- the present invention relates to a white polyester film suitable for use as a light reflecting plate, a light reflecting plate using the same, and a backlight for a liquid crystal display.
- a backlight method in which light is applied from the back of the display and a light reflecting plate are widely used because of a thin and uniform illumination.
- a light reflector on the back of the screen, but this reflector is required to be thin and have high light reflectivity.
- a white film or the like that is whitened by containing fine bubbles inside and reflecting light at the bubble interface is mainly used.
- the light reflected by the reflector is diffused, and the light other than the light that has directivity directly is reflected by the prism, and is repeatedly reflected between the reflector and finally the liquid crystal cell with enhanced light directivity. Sent to. In this case, if the reflection efficiency of the reflector is low, or if there is a factor that causes light leakage or attenuation in the system, light loss will occur during repeated reflections and the energy efficiency will deteriorate, reducing the brightness of the screen. Or the economy is reduced.
- Such a white polyester film is also used for a back sheet of a solar cell.
- Patent Document 1 describes that a light reflecting plate is used as one member constituting a light source of a liquid crystal display.
- Patent Document 2 describes that a white film whitened by containing fine bubbles inside the film and reflecting light at the bubble interface is used as the light reflecting plate.
- Patent Documents 3 and 4 describe a white film in which an ultraviolet absorbing layer is laminated in order to prevent yellow discoloration of the film due to ultraviolet rays emitted from a cold cathode tube.
- Patent Document 5 discloses a method of providing a light concealing layer on a film surface opposite to a light source in order to improve luminance in an edge light system.
- Patent Document 6 discloses a method of controlling the light diffusibility by selecting the refractive index difference between the spherical particles and the binder and improving the front luminance by the light diffusion sheet.
- Patent Document 7 discloses a method of improving luminance unevenness in a backlight by controlling the diffusibility of a film surface on the light source side in a reflection sheet in a direct type backlight.
- Patent Document 1 The reflector described in Patent Document 1 was not sufficiently thin and highly reflective.
- an ultraviolet absorbing layer is provided, or in a method in which the ultraviolet absorbing layer contains a trace amount of a fluorescent brightening agent, the absorbed ultraviolet energy is converted into heat, or the reflective film
- the brightness of the screen is reduced because only a small amount of light that contributes to color adjustment is converted.
- the reflectors described in Patent Documents 5 and 6 have a problem that the color change due to ultraviolet rays radiated from the cold cathode fluorescent lamp is large, and the use efficiency of light energy as a backlight is deteriorated and the luminance of the screen is lowered.
- Patent Document 7 contains porous and hollow particles and particles with non-uniform shapes together with a small amount of fluorescent brightening agent, even with a small amount of light that contributes to color adjustment, depending on the contained particles There has been a problem that light is attenuated by refraction, reflection, scattering, and the like, and the luminance is not improved.
- the white film In the reflection plate, it is necessary to prevent the white film from being deteriorated by the ultraviolet light (hereinafter referred to as UV) emitted from the lamp light source or with the white film while improving the reflection efficiency of the white film.
- UV ultraviolet light
- a conventionally known method for example, as disclosed in the aforementioned Patent Documents 3 and 4, a method of reducing the amount of ultraviolet rays reaching the polyester resin by thickly applying a layer containing a UV absorber to a white film was there.
- the layer containing the UV absorber is processed by post-processing, there is a problem in economic efficiency and lead time.
- the film used as the reflector is desirably thin from the viewpoints of miniaturization and weight reduction and processability.
- the reflection efficiency is lowered, so that the leakage needs to be suppressed as much as possible.
- the present invention eliminates the disadvantages of these conventional techniques, has high brightness, has little color change due to ultraviolet rays from the lamp or the sun, can prevent light leakage to the back surface, and further requires no post-processing, and is a white polyester film
- the purpose is to provide.
- an object of the present invention is a white polyester film having at least two layers of an A layer composed of polyester and a B layer composed of polyester, wherein the B layer has bubbles, and the A layer is rutile.
- the total thickness of the white polyester film is 100 ⁇ m or more and 500 ⁇ m or less
- the thickness of the A layer is 2 ⁇ m or more and 16 ⁇ m or less Is done.
- the object of the present invention is achieved by a light reflector using the above white polyester film.
- the object of the present invention is achieved by a backlight for a liquid crystal display in which the white polyester film is arranged with the layer A side facing the light source.
- the A layer contains 2 to 6% by mass of the rutile-type titanium oxide with respect to the total mass of the A layer, and the barium sulfate to the total mass of the A layer.
- the rutile titanium oxide preferably has a number average particle size of 0.1 ⁇ m or more and 1.0 ⁇ m or less.
- the barium sulfate preferably has a number average particle diameter of 0.5 ⁇ m to 3.0 ⁇ m.
- the number average particle diameter of the silicon dioxide is preferably 2.0 ⁇ m or more and 5.0 ⁇ m or less.
- the layer B preferably contains a polymer incompatible with polyester, or a polymer incompatible with polyester and inorganic particles dispersed therein.
- the white polyester film of the present invention is obtained by irradiating the layer A with ultraviolet rays under the conditions of illuminance: 100 mW / cm 2 , temperature: 60 ° C., relative humidity: 50% RH, and irradiation time: 48 hours. Yellowish change amount after UV irradiation: ⁇ b value is preferably less than 5.
- a white polyester film that has high brightness, little color change due to ultraviolet rays from a lamp or the sun, can prevent light leakage to the back surface, and does not require post-processing.
- the white polyester film of the present invention is suitably used for a large direct light type liquid crystal display used for televisions and the like, and a small sidelight type liquid crystal display used for notebook computers, mobile phones and the like. Moreover, it can be used as a back sheet for solar cells, and contributes to the efficiency of conversion from sunlight to electricity, and can impart resistance to ultraviolet rays from sunlight.
- the white polyester film of the present invention is a white polyester film having at least a layer A composed of polyester and a layer B composed of polyester, wherein the layer B has bubbles, and the layer A is a rutile titanium oxide, Three types of inorganic particles of barium sulfate and silicon dioxide are contained, the total thickness of the white polyester film is 100 ⁇ m or more and 500 ⁇ m or less, and the thickness of the A layer is 2 ⁇ m or more and 16 ⁇ m or less.
- the A layer is a layer in which inorganic particles are contained in polyester, and has a role of scattering the light and protecting the film from ultraviolet rays. It also has a role of preventing light leakage to the back surface and a role of a support layer for stabilizing the film formation.
- the light scattering property of the A layer can be adjusted mainly by controlling the surface roughness.
- a method of adding particles having different refractive indexes to a polyester resin can be mentioned.
- the thickness of the A layer is 2 ⁇ m or more and 16 ⁇ m or less.
- the B layer is a layer having bubbles. Therefore, if the thickness of the A layer is 2 ⁇ m or more and 16 ⁇ m or less, moderate irregularities are formed on the surface of the A layer due to the bubbles, The scattering property is extremely good.
- inorganic particles having an ultraviolet absorbing ability and a light stabilizer are included, a film having good resistance to ultraviolet rays and high brightness can be obtained.
- the A layer is disposed on the light source side, the A layer is gradually decomposed by the energy of ultraviolet rays.
- a preferable range of the thickness of the A layer is 2 ⁇ m or more and 8 ⁇ m or less, and more preferably 2 ⁇ m or more and 6 ⁇ m or less.
- the thickness of the A layer that is directed to the light source side at least at the outermost layer is 2 ⁇ m or more and 16 ⁇ m or less. Need to be. As described above, when the thickness of the A layer is less than 2 ⁇ m, the photolysis of the polyester has an adverse effect on the luminance, and the high luminance cannot be maintained. On the other hand, when the thickness of the A layer exceeds 16 ⁇ m, the loss of light energy in the A layer cannot be ignored, and the light does not sufficiently reach the voids in the B layer.
- the total thickness of the white polyester film of the present invention is 100 ⁇ m or more and 500 ⁇ m or less. If the total thickness of the white polyester film is less than 100 ⁇ m, the reflectance is insufficient.
- the upper limit is not particularly limited, but if the thickness exceeds 500 ⁇ m, no increase in reflectance can be expected even if the thickness is increased beyond this, and therefore the upper limit is usually 500 ⁇ m.
- the surface of the layer A is arranged toward the light source side, so that UV resistance, reduction in luminance unevenness, high reflectance, scratches on the light guide plate, and suppression of occurrence of uneven contact screen are suppressed.
- the layer structure may be a two-layer structure of A layer / B layer, a three-layer structure of A layer / B layer / A layer, or a structure of four or more layers, but it is easy on film formation. Considering this, a three-layer structure is preferable.
- the resin constituting the A layer and the B layer is polyester.
- polyethylene terephthalate and polyethylene naphthalate are preferable.
- additives such as an antioxidant and an antistatic agent may be added to the polyester.
- the B layer is whitened by containing fine bubbles inside the film.
- the formation of fine bubbles is caused by finely dispersing a polymer incompatible with polyester or a polymer incompatible with polyester and inorganic particles in a film base material such as polyester and stretching it (for example, biaxially). This can be achieved by stretching.
- the layer A contains rutile type titanium oxide.
- rutile type titanium oxide When rutile type titanium oxide is used, there is less yellowing after irradiating the polyester film with light for a longer time than when anatase type titanium oxide is used, and the change in color difference can be suppressed.
- this rutile-type titanium oxide is used after being treated with a fatty acid such as stearic acid or a derivative thereof, the dispersibility can be improved and the glossiness of the film can be further improved.
- the number average particle diameter (diameter) of rutile type titanium oxide is preferably 0.1 ⁇ m or more and 1.0 ⁇ m or less. When the number average particle diameter of rutile type titanium oxide is within this range, aggregation is difficult to occur, uniform dispersibility is good, and light resistance is excellent, while film stretchability is also good, productivity is high, and light resistance is excellent. .
- the addition amount of rutile type titanium oxide is preferably 2% by mass or more and 6% by mass or less with respect to the mass of the entire A layer.
- the addition amount of rutile-type titanium oxide is within this range, the stretchability of the film is good, and even after the polyester film is irradiated with light for a long time, there is little yellowing and the change in color difference can be suppressed. Further, it is difficult to cause a reduction in reflection performance and luminance unevenness, and the screen luminance can be improved.
- the white polyester film of the present invention is complementary because of reduced reflection performance and uneven brightness. It is necessary to combine barium sulfate. Thus, when barium sulfate is complementarily combined, a favorable reflectance can be obtained and luminance unevenness can be reduced. Since barium sulfate is incompatible with polyester, many fine bubbles can exist even in the A layer, and there is little yellowing after irradiating the polyester film with light for a long time, suppressing the change in color difference. it can.
- the number average particle diameter (diameter) of barium sulfate is preferably 0.5 ⁇ m or more and 3.0 ⁇ m or less.
- the addition amount of barium sulfate is preferably 16% by mass or more and 24% by mass or less with respect to the total mass of the A layer.
- the reflectance does not decrease, the yellowing after irradiating the polyester film with light for a long time is small, and it is easy to suppress the change in color difference. The stretchability is not impaired and the productivity is good.
- the white film surface that is, the surface of the layer A has a certain degree of roughness, and is easily available for the purpose of reducing the adhesion between the screen and the white film.
- the number average particle diameter (diameter) of silicon dioxide is preferably 2.0 ⁇ m or more and 5.0 ⁇ m or less.
- the direct reflection component does not increase excessively, and the difference in brightness (brightness unevenness) according to the interval between the illumination light sources hardly occurs, so that the brightness of the liquid crystal screen can be kept uniform.
- particles that have become too coarse will not fall off, and the light guide plate will not be scratched.
- the direct type since there is a cold cathode tube between the light guide plate and the reflection plate, the light guide plate and the reflection plate are not in direct contact with each other, and there is no worry about the occurrence of scratches on the light guide plate and uneven contact screen.
- the content of silicon dioxide is preferably 0.5% by mass or more and 3% by mass or less with respect to the mass of the entire A layer.
- the content of silicon dioxide is within this range, the surface roughness becomes too low and luminance unevenness does not occur, and the brightness of the liquid crystal screen can be made uniform.
- the stretchability of the film is not impaired and the productivity is good.
- the total content of the three types of inorganic particles of rutile titanium oxide, barium sulfate and silicon dioxide per 100% by mass of the A layer is preferably 10% by mass or more and 50% by mass or less. More preferably, they are 12 mass% or more and 40 mass% or less, More preferably, they are 15 mass% or more and 30 mass% or less. When the total content of the inorganic particles is within this range, necessary UV resistance and reflectance can be easily obtained, while cutting during film formation hardly occurs.
- the white polyester film of the present invention has a configuration in which a plurality of A layers are present such as A layer / B layer / A layer
- the content of the aforementioned rutile titanium oxide, barium sulfate, and silicon dioxide is preferable.
- the preferable range and the preferred range of the number average particle diameter apply to the A layer directed to the light source side at least in the outermost layer.
- the white polyester film of the present invention has a yellowness change amount ( ⁇ b value) after irradiation with ultraviolet rays on layer A for illuminance: 100 mW / cm 2 , temperature: 60 ° C., relative humidity: 50% RH, irradiation time: 48 hours. Preferably it is less than 5.
- the ⁇ b value is more preferably less than 4 and even more preferably less than 3.
- the lower limit is not particularly limited and is theoretically zero.
- the white polyester film of the present invention can easily achieve the above ⁇ b value by using three kinds of inorganic particles of rutile type titanium oxide, barium sulfate and silicon dioxide in combination. Even so, it is useful in that the color change can be reduced. Moreover, there is almost no loss of luminance as a reflector.
- Cyclic olefin as an incompatible polymer polyethylene glycol, polybutylene terephthalate and polytetramethylene glycol copolymer as a low specific gravity agent are mixed with polyethylene terephthalate, thoroughly mixed and dried, and a temperature of 270 to 300 ° C.
- barium sulfate and silicon dioxide is supplied to the extruder A by a conventional method, and the polymer of the extruder B layer is formed on both surface layers in the T-die three-layer die. A three-layer structure of A layer / B layer / A layer was obtained.
- the melted sheet is closely cooled and solidified by electrostatic force on a drum cooled to a drum surface temperature of 10 to 60 ° C., and the unstretched film is led to a group of rolls heated to 80 to 120 ° C. in the longitudinal direction.
- the film is stretched 2.0 to 5.0 times in length and cooled with a roll group of 20 to 50 ° C. Subsequently, the film is stretched in the direction perpendicular to the longitudinal direction in an atmosphere heated to 90 to 140 ° C. while being guided to a tenter while holding both ends of the film that has been stretched with clips.
- the stretching ratio is 2.5 to 4.5 times in the longitudinal and lateral directions, and the area ratio (longitudinal stretching ratio ⁇ lateral stretching ratio) is preferably 9 to 16 times.
- the white polyester film of the present invention preferably has an average reflectance of 90% or more, more preferably 95% or more, and particularly preferably 97% or more at a wavelength of 400 to 700 nm as measured from the layer A surface.
- the average reflectance is less than 90%, the luminance may be insufficient depending on the applied liquid crystal display.
- the white polyester film of the present invention thus obtained can improve the luminance of the liquid crystal backlight, and since the reflectance does not decrease much even when used for a long time, the edge light and the direct type light for liquid crystal screens. It can be conveniently used as a reflector for a surface light source and a reflector.
- the white polyester film for reflecting a liquid crystal display according to the present invention thus obtained has a high reflectance because fine bubbles are formed inside the film, and is used as a reflector for liquid crystal displays of side light type and direct light type. In this case, high brightness can be obtained.
- the physical property value evaluation method and the effect evaluation method of the present invention are as follows. (1) Film thickness / layer thickness The film thickness was measured according to JIS C2151-2006.
- the film was cut in the thickness direction using a microtome to obtain a section sample.
- the section of the slice sample was imaged at a magnification of 3,000 times using a Hitachi Field Emission Scanning Electron Microscope (FE-SEM) S-800, and the thickness of each layer was measured and the thickness ratio was calculated by measuring the thickness of the laminate. .
- FE-SEM Hitachi Field Emission Scanning Electron Microscope
- An integrating sphere is attached to a spectrophotometer (U-3310) manufactured by Hitachi High-Technologies, and the reflectance when the standard white plate (aluminum oxide) is 100% is measured over a wavelength range of 400 to 700 nm. The reflectance was read from the obtained chart at intervals of 5 nm to obtain spectral reflectance.
- the reflecting plate laminated in the backlight of 181BLM07 manufactured by NEC Corporation
- the backlight is formed by stacking elements of the light reflecting white polyester film 1, the cold cathode tube 2, the milky white plate 3, the diffusion plate 4, the prism sheet 5, and the polarizing prism sheet 6 in order from the bottom to the top in FIG. Composed.
- the liquid crystal screen was photographed with a CCD camera 7 (DXC-390 manufactured by SONY), and an image was captured with an eye scale 8 manufactured by an image analyzer Eye System. Thereafter, the luminance level of the photographed image was controlled to 30,000 steps and automatically detected, and converted into luminance to obtain the relative luminance value (%).
- Relative luminance was determined by the following standard using # 250E6SL manufactured by Toray Industries, Inc. as a reference sample (100%).
- luminance unevenness (%) was obtained by the following equation.
- Unevenness of luminance (%) (maximum relative luminance value ⁇ minimum relative luminance value) / average relative luminance value ⁇ 100
- the brightness unevenness was determined according to the following criteria using # 250E6SL manufactured by Toray Industries, Inc. as a reference sample (100%).
- the number average diameter when each particle was converted to a perfect circle was calculated and used as the average particle diameter of the inorganic particles.
- Yellowness (b value), ⁇ b value Using an SM color computer (manufactured by Suga Test Instruments Co., Ltd.), a b value representing yellowness was determined by a reflection measurement method using a C / 2 ° light source.
- Light resistance (yellowishness change: ⁇ b value) Light resistance was evaluated by irradiating the sample with ultraviolet rays using an iSuper UV tester (model number: SUV-W131) manufactured by Iwasaki Electric Co., Ltd. and measuring the color tone b value before and after the irradiation.
- the change in b value before and after UV irradiation was defined as ⁇ b. That is, as shown in the following equation, the ⁇ b value is the difference between the yellowness b 2 after UV irradiation and the initial yellowness b 1 .
- ⁇ b value yellowness b 2 after UV irradiation ⁇ initial yellowness b 1
- the ultraviolet irradiation conditions were as follows.
- Illuminance 100 mW / cm 2 , temperature: 60 ° C., relative humidity: 50% RH, irradiation time: 48 hours
- Light resistance was graded according to the following criteria.
- the film can be stably formed for 24 hours or more.
- the film can be stably formed for 12 hours or more and less than 24 hours.
- the presence or absence of scratches was visually confirmed, and the light guide plate scratches were determined according to the following criteria.
- Example 1 Polyethylene glycol having a molecular weight of 4,000 and having a color tone of polyethylene terephthalate after polymerization (JIS K7105-1981, measured by stimulus value direct reading method) of L value 62.8, b value 0.5, haze 0.2% Using terephthalate, 57 parts by mass of polyethylene terephthalate, 10 parts by mass of (PBT / PTMG) copolymer of polybutylene terephthalate and polytetramethylene glycol (trade name: Hytrel manufactured by Toray DuPont Co., Ltd.), against ethylene glycol 10 parts by mass of copolymerized polyethylene terephthalate (33 mol% CHDM copolymerized PET) in which 33 mol% of 1,4-cyclohexanedimethanol was copolymerized and 23 parts by mass of poly (5-methyl) norbornene were prepared and mixed at 180 ° C. for 3 hours. After drying,
- Extruder A heated to 280 ° C. (A layer).
- a layer A layer
- the unstretched film obtained by cooling and solidifying this film with a cooling drum having a surface temperature of 25 ° C. was led to a roll group heated to 85 to 98 ° C., longitudinally stretched 3.7 times in the longitudinal direction, and cooled with a roll group at 21 ° C. . Subsequently, the film was stretched by 3.6 times in a direction perpendicular to the longitudinal direction in an atmosphere heated to 120 ° C.
- Examples 2 to 30 A white polyester film was obtained in the same manner as in Example 1, except that the raw material composition of the A layer and B layer, the thickness of the A layer, and the total film thickness were changed as described in Table 1.
- Example 1 since the content of silicon dioxide was small, the luminance unevenness was slightly inferior, and since the content of rutile-type titanium oxide was small, the light resistance was slightly lower than the other examples. It was inferior. Although the content of barium sulfate was small, the luminance was at a level that could be used practically.
- Example 2 since the contents of silicon dioxide and barium sulfate were larger, the film-forming stability was slightly inferior to those of the other examples, and the content of rutile titanium oxide was larger. was slightly inferior to the other examples.
- Example 3 since the number average particle diameter of silicon dioxide was smaller, the luminance unevenness was slightly inferior to the other examples, and the number average particle diameter of rutile-type titanium oxide was smaller, so that the light resistance was high. It was slightly inferior to the other examples. Although the number average particle size of barium sulfate was smaller, the luminance was at a level that could be used practically.
- Example 4 since the number average molecular weights of silicon dioxide and barium sulfate were larger, the film-forming stability was slightly inferior to the other examples, and the number average particle diameter of rutile titanium oxide was larger. Therefore, the light resistance was slightly inferior to the other examples.
- Example 5 since the content of silicon dioxide was small, the luminance unevenness was slightly inferior to the other examples, and the content of rutile type titanium oxide was small, so that the light resistance was another example. Was slightly inferior to. Although the content of barium sulfate was small, the luminance was at a level that could be used practically.
- Example 6 since the contents of silicon dioxide and barium sulfate were higher, the film-forming stability was slightly inferior to those of the other examples, and the content of rutile titanium oxide was higher. was slightly inferior to the other examples.
- Example 7 since the number average particle diameter of silicon dioxide was smaller, the luminance unevenness was slightly inferior to the other examples, and the number average particle diameter of rutile-type titanium oxide was smaller, so that the light resistance was high. It was slightly inferior to the other examples. Although the number average particle size of barium sulfate was smaller, the luminance was at a level that could be used practically.
- Example 8 since the number average molecular weights of silicon dioxide and barium sulfate were larger, the film forming stability was slightly inferior to those of the other examples. Although the number average particle size of rutile type titanium oxide was large, the light resistance was at a level that could be used practically.
- Comparative Example 1 A film having a thickness of 188 ⁇ m was obtained in the same manner as in Example 1 except that the laminated structure and the raw material composition were changed as described in Table 1. Although the film formation is stable and the relative reflectance is 104.2% and high luminance is obtained even in the relative luminance, the silicon dioxide is not added to the A layer. It was insufficient.
- Example 2 A film having a thickness of 188 ⁇ m was obtained in the same manner as in Example 1 except that the laminated structure and the raw material composition were changed as described in Table 1. Although the relative reflectance was 104.3% and a high value was obtained even in the relative luminance, the light resistance was insufficient because no rutile-type titanium oxide was added to the A layer.
- Comparative Example 3 A film having a thickness of 188 ⁇ m was obtained in the same manner as in Example 1 except that the laminated structure and the raw material composition were changed as described in Table 1.
- Example 5 A film having a thickness of 188 ⁇ m was obtained in the same manner as in Example 1 except that the laminated structure and the raw material composition were changed as described in Table 1. The film was stable, the relative reflectance was 103.8%, and a high luminance was obtained even with the relative luminance, but the luminance unevenness was insufficient because the A layer was thick.
- Comparative Example 6 A film having a thickness of 250 ⁇ m was obtained in the same manner as in Example 1 except that the laminated structure and the raw material composition were changed as described in Table 1. Although the relative reflectance was 102.0% and the relative luminance was also high, there was a scratch on the light guide plate because no silicon dioxide was added to the A layer, and no rutile titanium oxide was added.
- Example 7 A film having a thickness of 225 ⁇ m was obtained in the same manner as in Example 1 except that the laminated structure and the raw material composition were changed as described in Table 1. However, in order to obtain a two-layer lamination of A / B layers, lamination was performed with a feed block, and a sheet was extruded from a T-die to obtain a molten sheet. Although the film-forming stability was insufficient, the relative reflectance was 103.0%, and a high value was obtained even in the relative luminance, but there was a scratch on the light guide plate and the light resistance was insufficient.
- Example 8 A film having a thickness of 225 ⁇ m was obtained in the same manner as in Example 1 except that the laminated structure and the raw material composition were changed as described in Table 1. However, since the raw material was not supplied to the extruder A and the A layer was not formed, it became a single layer film of only the B layer. There was film-forming stability, the relative reflectance was 100.0%, there were scratches on the light guide plate, and the relative luminance, luminance unevenness and light resistance were insufficient.
- PET Polyethylene terephthalate
- PET / I / PEG ethylene glycol / terephthalic acid / isophthalic acid cocondensate (polyethylene terephthalate copolymer in which 5 mol% of polyethylene glycol having a molecular weight of 1,000 is copolymerized)
- PET / CHDM polyethylene-1,4-cyclohexylenedimethylene terephthalate (polyethylene terephthalate copolymer obtained by copolymerizing 33 mol% of 1,4-cyclohexanedimethanol with respect to ethylene glycol)
- PBT / PTMG Polyester ether elastomer mabutylene / poly (alkylene ether) phthalate (copolymer having 30 mol% of alkylene glycol with respect to butylene terephthalate) (trade name: Hytrel manufactured by Toray DuPont) It is.
- the white polyester film of the present invention is suitably used for large direct-type light-type liquid crystal displays used for televisions and the like, and small sidelight-type liquid crystal displays used for notebook computers and mobile phones. Moreover, it can be used as a back sheet for solar cells, and contributes to the efficiency of conversion from sunlight to electricity, and can impart resistance to ultraviolet rays from sunlight.
Abstract
Description
変換するか、反射フィルムの色目調整に寄与する少量の光量にしか変換されず画面の輝度が低下する問題があった。
特許文献5,6に記載の反射板は冷陰極管から放射される紫外線による色調変化が大きく、バックライトとしての光エネルギーの利用効率が悪くなって画面の輝度が低下する問題があった。
特許文献7に記載の反射板は微量の蛍光増白剤と共に多孔質や中空の粒子や形状が不均一な粒子を含有したものは、色目調整に寄与する少量の光量でさえ、含有した粒子によって屈折や反射や散乱等によって光が減衰し輝度が向上しないという問題があった。 In the reflectors described in
The reflectors described in
The reflector described in
〔物性の測定ならびに効果の評価方法〕
本発明の物性値の評価方法ならびに効果の評価方法は次の通りである。
(1)フィルム厚み・層厚み
フィルムの厚みは、JIS C2151-2006に準じて測定した。 The white polyester film of the present invention thus obtained can improve the luminance of the liquid crystal backlight, and since the reflectance does not decrease much even when used for a long time, the edge light and the direct type light for liquid crystal screens. It can be conveniently used as a reflector for a surface light source and a reflector. The white polyester film for reflecting a liquid crystal display according to the present invention thus obtained has a high reflectance because fine bubbles are formed inside the film, and is used as a reflector for liquid crystal displays of side light type and direct light type. In this case, high brightness can be obtained.
[Measurement of physical properties and evaluation method of effects]
The physical property value evaluation method and the effect evaluation method of the present invention are as follows.
(1) Film thickness / layer thickness The film thickness was measured according to JIS C2151-2006.
該切片サンプルの断面を日立製作所製電界放射型走査電子顕微鏡(FE-SEM)S-800を用いて、3,000倍の倍率で撮像し、撮像から積層厚みを採寸し各層厚みと厚み比を算出した。
(2)相対平均反射率
日立ハイテクノロジーズ製分光光度計(U―3310)に積分球を取り付け、標準白色板(酸化アルミニウム)を100%とした時の反射率を波長400~700nmにわたって測定する。得られたチャートより5nm間隔で反射率を読み取り、分光反射率とした。
(3)見かけ比重
フィルムを100×100mm角に切取り、ダイアルゲージを取り付けたものにて10点の厚みを測定し、厚みの平均値d(μm)を計算する。また、このフィルムを直示天秤にて秤量し、重さw(g)を10-4gの単位まで読み取る。このとき、見かけ比重を次式により求めた。 The film was cut in the thickness direction using a microtome to obtain a section sample.
The section of the slice sample was imaged at a magnification of 3,000 times using a Hitachi Field Emission Scanning Electron Microscope (FE-SEM) S-800, and the thickness of each layer was measured and the thickness ratio was calculated by measuring the thickness of the laminate. .
(2) Relative average reflectance An integrating sphere is attached to a spectrophotometer (U-3310) manufactured by Hitachi High-Technologies, and the reflectance when the standard white plate (aluminum oxide) is 100% is measured over a wavelength range of 400 to 700 nm. The reflectance was read from the obtained chart at intervals of 5 nm to obtain spectral reflectance.
(3) Apparent specific gravity A film is cut into a 100 × 100 mm square, 10 points of thickness are measured with a dial gauge attached, and an average thickness d (μm) is calculated. Further, this film is weighed with a direct balance, and the weight w (g) is read to a unit of 10 −4 g. At this time, the apparent specific gravity was determined by the following equation.
(4)相対輝度および輝度ムラ(直下型方式輝度)
図1に示したように181BLM07(NEC(株)製)のバックライト内に張り合わせてある反射板を所定の光反射用白色ポリエステルフィルム1のサンプルに変更し、点灯させた。ここで、バックライトは、図1において下から上の順に、光反射用白色ポリエステルフィルム1、冷陰極管2、乳白板3、拡散板4、プリズムシート5、偏光プリズムシート6の要素を積み重ねて構成される。点灯状態で1時間待機して光源を安定化させた後、液晶画面部をCCDカメラ7(SONY製DXC-390)にて撮影し、画像解析装置アイシステム製アイスケール8で画像を取り込んだ。その後、撮影した画像の輝度レベルを3万ステップに制御し自動検出させ、輝度に変換して相対輝度の値(%)を求めた。 Apparent specific gravity = w / d × 100
(4) Relative luminance and luminance unevenness (direct type luminance)
As shown in FIG. 1, the reflecting plate laminated in the backlight of 181BLM07 (manufactured by NEC Corporation) was changed to a predetermined sample of
B:101%以上102%未満
C:100%以上101%未満
F:100%未満。 A: 102% or more B: 101% or more and less than 102% C: 100% or more and less than 101% F: Less than 100%.
輝度ムラは、東レ株式会社製#250E6SLを基準サンプル(100%)とし、次の基準で級判定した。 Unevenness of luminance (%) = (maximum relative luminance value−minimum relative luminance value) / average relative luminance value × 100
The brightness unevenness was determined according to the following criteria using # 250E6SL manufactured by Toray Industries, Inc. as a reference sample (100%).
B:80%以上90%未満
C:90%以上100%未満
F:100%以上。
(5)フィルム中の無機粒子の平均粒径(直径)
透過型電子顕微鏡HU-12型((株)日立製作所製)を用い、A層およびB層の断面を10,0000倍に拡大観察した断面写真から求めた。すなわち、断面写真の粒子部分を粒子形状に沿ってマーキングして、その粒子部分をハイビジョン画像解析処理装置PIAS-IV((株)ピアス製)を用いて画像処理を行い、測定視野内の計100個の粒子を真円に換算した時の数平均径を算出し、無機粒子の平均粒径とした。
(6)黄色味(b値)、Δb値
SMカラーコンピューター(スガ試験機(株)製)を用い、C/2°光源による反射測定法により、黄色味を表すb値を求めた。
(7)耐光性(黄色味変化:Δb値)
岩崎電気(株)製アイスーパーUVテスター(型番:SUV-W131)を用いてサンプルに紫外線を照射し、照射前後の色調b値を測定することで、耐光性の評価を行った。紫外線照射前後のb値の変化をΔbとした。すなわち、Δb値は、次式に示すとおり、UV照射後の黄色味b2と初期の黄色味b1との差をいう。 A: Less than 80% B: 80% or more and less than 90% C: 90% or more and less than 100% F: 100% or more.
(5) Average particle diameter (diameter) of inorganic particles in the film
Using a transmission electron microscope HU-12 type (manufactured by Hitachi, Ltd.), it was determined from a cross-sectional photograph obtained by observing the cross sections of the A layer and the B layer at a magnification of 10,0000. That is, the particle portion of the cross-sectional photograph is marked along the particle shape, and the particle portion is subjected to image processing using a high-definition image analysis processing device PIAS-IV (manufactured by Pierce Co., Ltd.). The number average diameter when each particle was converted to a perfect circle was calculated and used as the average particle diameter of the inorganic particles.
(6) Yellowness (b value), Δb value Using an SM color computer (manufactured by Suga Test Instruments Co., Ltd.), a b value representing yellowness was determined by a reflection measurement method using a C / 2 ° light source.
(7) Light resistance (yellowishness change: Δb value)
Light resistance was evaluated by irradiating the sample with ultraviolet rays using an iSuper UV tester (model number: SUV-W131) manufactured by Iwasaki Electric Co., Ltd. and measuring the color tone b value before and after the irradiation. The change in b value before and after UV irradiation was defined as Δb. That is, as shown in the following equation, the Δb value is the difference between the yellowness b 2 after UV irradiation and the initial yellowness b 1 .
ここで、紫外線照射条件を次のとおりとした。 Δb value = yellowness b 2 after UV irradiation−initial yellowness b 1
Here, the ultraviolet irradiation conditions were as follows.
耐光性を下記基準により級判定した。 Illuminance: 100 mW / cm 2 , temperature: 60 ° C., relative humidity: 50% RH, irradiation time: 48 hours Light resistance was graded according to the following criteria.
B:黄色味変化量Δb値が3以上4未満
C:黄色味変化量Δb値が4以上5未満
F:黄色味変化量Δb値が5以上
(8)製膜安定性
安定に製膜できるか否かの程度を次の基準により級判定した。 A: Yellowish change Δb value is less than 3 B: Yellowish change Δb value is 3 or more and less than 4 C: Yellowish change Δb value is 4 or more and less than 5 F: Yellowish change Δb value is 5 or more (8 ) Film formation stability The grade of whether or not the film can be stably formed was determined according to the following criteria.
(9)導光板キズ(サイドライト方式)
図2に示したようなソニー(株)製VAIO(VGN-S52B/S)のバックライト内に張り合わせてある反射板を所定の光反射用白色ポリエステルフィルム10のサンプルに変更し、導光板13に接触させた後、光反射用白色ポリエステルフィルムを外して、導光板の表面を観察した。ここで、バックライトは、図2において下から上の順に、冷陰極管9、光反射用白色ポリエステルフィルム10、導光板11、プリズムシート12の要素を積み重ねて構成される。 F: Breakage occurs within 12 hours, and stable film formation cannot be performed.
(9) Light guide plate scratches (side light method)
The reflective plate attached in the backlight of Sony Corporation VAIO (VGN-S52B / S) as shown in FIG. 2 is changed to a sample of a predetermined
B:少々のキズはあるが実用可能レベル
F:キズがあり実用不可能レベル A: No scratches B: Slight scratches but practical level F: Scratches practical level
[実施例1]
分子量4,000のポリエチレングリコールを使用し、重合後のポリエチレンテレフタレートの色調(JIS K7105-1981、刺激値直読方法で測定)がL値62.8、b値0.5、ヘイズ0.2%であるポリエチレンテレフタレートを使用し、ポリエチレンテレフタレート57質量部、ポリブチレンテレフタレートとポリテトラメチレングリコールの(PBT/PTMG)共重合物を10質量部(商品名:東レ・デュポン(株)製ハイトレル)、エチレングリコールに対し1,4-シクロヘキサンジメタノールが33mol%共重合された共重合ポリエチレンテレフタレート(33mol%CHDM共重合PET)10質量部、ポリ(5-メチル)ノルボルネン23質量部を調整混合し、180℃で3時間乾燥させた後、270~300℃に加熱された押出機Bに供給(B層)した。 The present invention will be described based on examples.
[Example 1]
Polyethylene glycol having a molecular weight of 4,000 and having a color tone of polyethylene terephthalate after polymerization (JIS K7105-1981, measured by stimulus value direct reading method) of L value 62.8, b value 0.5, haze 0.2% Using terephthalate, 57 parts by mass of polyethylene terephthalate, 10 parts by mass of (PBT / PTMG) copolymer of polybutylene terephthalate and polytetramethylene glycol (trade name: Hytrel manufactured by Toray DuPont Co., Ltd.), against
[実施例2~30]
A層、B層の原料組成、A層の厚み、フィルム全厚みを表1に記載したとおりに変更した以外は、実施例1と同様の方法で白色ポリエステルフィルムを得た。 Meanwhile, 38.7 parts by mass of 48.7 parts by mass of polyethylene terephthalate chips, 3 parts by mass of rutile titanium oxide polyethylene terephthalate master having a number average particle size of 0.25 μm (containing 36% by mass of rutile titanium oxide based on the total amount of master chips), 0.3 parts by mass of silicon dioxide particle polyethylene terephthalate master having a number average particle size of 3.5 μm (containing 6% by mass of silicon dioxide with respect to the total amount of the master chip) and barium sulfate particle polyethylene terephthalate master 16 having a number average particle size of 1.4 μm Parts by weight (containing 60% by weight of barium sulfate based on the total amount of the master chip), 17 parts by weight of polyethylene terephthalate copolymerized with 18 mol% of isophthalic acid (PET / I), and 1 part by weight of sodium dodecylbenzenesulfonate , Polyethylene terephthalate / polyethylene 14 parts by weight of the polyglycol polycondensate was vacuum-dried at 180 ° C. for 3 hours, and then supplied to Extruder A heated to 280 ° C. (A layer). These polymers were combined with A layer / B layer / A layer. It laminated | stacked so that it might become, and it shape | molded in the sheet form from T-die. Further, the unstretched film obtained by cooling and solidifying this film with a cooling drum having a surface temperature of 25 ° C. was led to a roll group heated to 85 to 98 ° C., longitudinally stretched 3.7 times in the longitudinal direction, and cooled with a roll group at 21 ° C. . Subsequently, the film was stretched by 3.6 times in a direction perpendicular to the longitudinal direction in an atmosphere heated to 120 ° C. while being guided to a tenter while holding both ends of the longitudinally stretched film with clips. Thereafter, the film was heat-set at 200 ° C. in a tenter, uniformly cooled, cooled to room temperature, and a biaxially stretched laminated film was obtained. The physical properties of the light reflecting substrate are shown in Table 1.
[Examples 2 to 30]
A white polyester film was obtained in the same manner as in Example 1, except that the raw material composition of the A layer and B layer, the thickness of the A layer, and the total film thickness were changed as described in Table 1.
[比較例1]
積層構成および原料組成を表1に記載したとおりに変更した以外は、実施例1と同様の方法で厚み188μmのフィルムを得た。製膜安定性があり、相対反射率は、104.2%、相対輝度でも高い輝度が得られたものの、A層に二酸化珪素を添加していないため導光板へのキズがあり、輝度ムラが不十分であった。
[比較例2]
積層構成および原料組成を表1に記載したとおりに変更した以外は、実施例1と同様の方法で厚み188μmのフィルムを得た。相対反射率は104.3%であり、相対輝度でも高い値が得られたものの、A層にルチル型酸化チタンを添加していないため耐光性が不十分であった。
[比較例3]
積層構成および原料組成を表1に記載したとおりに変更した以外は、実施例1と同様の方法で厚み188μmのフィルムを得た。製膜安定性があり、相対反射率は103.5%であり、相対輝度でも高い値が得られたものの、A層に硫酸バリウムを添加していないため、A層において微細な気泡を発現させることができず、耐光性が不十分であった。
[比較例4]
積層構成および原料組成を表1に記載したとおりに変更した以外は、実施例1と同様の方法で厚み188μmのフィルムを得た。製膜安定性があり、相対反射率は104.4%であり、相対輝度でも高い値が得られたものの、A層の厚みが薄いため製膜安定性が不足しており、耐光性も不十分であった。
[比較例5]
積層構成および原料組成を表1に記載した様に変更した他は、実施例1と同様の方法で厚み188μmのフィルムを得た。製膜安定性があり、相対反射率は、103.8%、相対輝度でも高い輝度が得られたが、A層の厚みが厚いため輝度ムラが不十分であった。
[比較例6]
積層構成および原料組成を表1に記載したとおりに変更した以外は、実施例1と同様の方法で厚み250μmのフィルムを得た。相対反射率は102.0%であり、相対輝度も高い値が得られたものの、A層に二酸化珪素を添加していないため導光板へのキズがあり、ルチル型酸化チタンを添加していないため耐光性が不十分であった。
[比較例7]
積層構成および原料組成を表1に記載したとおりに変更した以外は、実施例1と同様の方法で厚み225μmのフィルムを得た。ただし、A/B層の2層積層とするためフィードブロックにて積層し、Tダイよりシート状に押出して溶融シートとした。製膜安定性が不足しており、相対反射率は103.0%であり、相対輝度でも高い値が得られたものの、導光板へのキズがあり、耐光性が不十分であった。
[比較例8]
積層構成および原料組成を表1に記載したとおりに変更した以外は実施例1と同様の方法で厚み225μmのフィルムを得た。ただし、押出機Aには原料を供給せず、A層を形成していないので、B層のみの単層フィルムとなった。製膜安定性があり、相対反射率は100.0%であり、導光板へのキズがあり、相対輝度、輝度ムラおよび耐光性が不十分であった。 In Example 8, since the number average molecular weights of silicon dioxide and barium sulfate were larger, the film forming stability was slightly inferior to those of the other examples. Although the number average particle size of rutile type titanium oxide was large, the light resistance was at a level that could be used practically.
[Comparative Example 1]
A film having a thickness of 188 μm was obtained in the same manner as in Example 1 except that the laminated structure and the raw material composition were changed as described in Table 1. Although the film formation is stable and the relative reflectance is 104.2% and high luminance is obtained even in the relative luminance, the silicon dioxide is not added to the A layer. It was insufficient.
[Comparative Example 2]
A film having a thickness of 188 μm was obtained in the same manner as in Example 1 except that the laminated structure and the raw material composition were changed as described in Table 1. Although the relative reflectance was 104.3% and a high value was obtained even in the relative luminance, the light resistance was insufficient because no rutile-type titanium oxide was added to the A layer.
[Comparative Example 3]
A film having a thickness of 188 μm was obtained in the same manner as in Example 1 except that the laminated structure and the raw material composition were changed as described in Table 1. Although there is film-forming stability, the relative reflectance is 103.5%, and a high value is obtained even in the relative luminance, but since no barium sulfate is added to the A layer, fine bubbles are expressed in the A layer. The light resistance was insufficient.
[Comparative Example 4]
A film having a thickness of 188 μm was obtained in the same manner as in Example 1 except that the laminated structure and the raw material composition were changed as described in Table 1. Although it has film-forming stability, the relative reflectance is 104.4%, and a high value is also obtained in the relative luminance, but the film-forming stability is insufficient because the thickness of the A layer is thin, and the light resistance is not good. It was enough.
[Comparative Example 5]
A film having a thickness of 188 μm was obtained in the same manner as in Example 1 except that the laminated structure and the raw material composition were changed as described in Table 1. The film was stable, the relative reflectance was 103.8%, and a high luminance was obtained even with the relative luminance, but the luminance unevenness was insufficient because the A layer was thick.
[Comparative Example 6]
A film having a thickness of 250 μm was obtained in the same manner as in Example 1 except that the laminated structure and the raw material composition were changed as described in Table 1. Although the relative reflectance was 102.0% and the relative luminance was also high, there was a scratch on the light guide plate because no silicon dioxide was added to the A layer, and no rutile titanium oxide was added. Therefore, the light resistance was insufficient.
[Comparative Example 7]
A film having a thickness of 225 μm was obtained in the same manner as in Example 1 except that the laminated structure and the raw material composition were changed as described in Table 1. However, in order to obtain a two-layer lamination of A / B layers, lamination was performed with a feed block, and a sheet was extruded from a T-die to obtain a molten sheet. Although the film-forming stability was insufficient, the relative reflectance was 103.0%, and a high value was obtained even in the relative luminance, but there was a scratch on the light guide plate and the light resistance was insufficient.
[Comparative Example 8]
A film having a thickness of 225 μm was obtained in the same manner as in Example 1 except that the laminated structure and the raw material composition were changed as described in Table 1. However, since the raw material was not supplied to the extruder A and the A layer was not formed, it became a single layer film of only the B layer. There was film-forming stability, the relative reflectance was 100.0%, there were scratches on the light guide plate, and the relative luminance, luminance unevenness and light resistance were insufficient.
PET:ポリエチレンテレフタレート、
PET/I/PEG:エチレングリコール/テレフタル酸/イソフタル酸共縮合物(分子量1,000のポリエチレングリコール5mol%が共重合されたポリエチレンテレフタレート共重合体)、
PET/CHDM:ポリエチレン-1,4-シクロヘキシレンジメチレンテレフタレート(エチレングリコールに対し1,4-シクロヘキサンジメタノールが33mol%共重合されたポリエチレンテレフタレート共重合体)、
PBT/PTMG:ポリエステルエーテルエラストマブチレン/ポリ(アルキレンエーテル)フタレート(ブチレンテレフタレートに対し、アルキレングリコールが30mol%の共重合体)(商品名:東レデュポン社製ハイトレル)、
である。 Here, the abbreviations in Tables 1 to 4 represent the following contents. That is,
PET: Polyethylene terephthalate,
PET / I / PEG: ethylene glycol / terephthalic acid / isophthalic acid cocondensate (polyethylene terephthalate copolymer in which 5 mol% of polyethylene glycol having a molecular weight of 1,000 is copolymerized),
PET / CHDM: polyethylene-1,4-cyclohexylenedimethylene terephthalate (polyethylene terephthalate copolymer obtained by copolymerizing 33 mol% of 1,4-cyclohexanedimethanol with respect to ethylene glycol),
PBT / PTMG: Polyester ether elastomer mabutylene / poly (alkylene ether) phthalate (copolymer having 30 mol% of alkylene glycol with respect to butylene terephthalate) (trade name: Hytrel manufactured by Toray DuPont)
It is.
2:冷陰極管
3:乳白板
4:拡散板
5:プリズムシート
6:偏光プリズムシート
7:CCDカメラ
8:画像解析装置(アイスケール)
9:冷陰極管
10:光反射用白色ポリエステルフィルム
11:導光板
12:プリズムシート
13:CCDカメラ 1: White polyester film for light reflection 2: Cold cathode tube 3: Milky white plate 4: Diffuser plate 5: Prism sheet 6: Polarizing prism sheet 7: CCD camera 8: Image analyzer (eye scale)
9: Cold cathode tube 10: White polyester film for light reflection 11: Light guide plate 12: Prism sheet 13: CCD camera
Claims (9)
- ポリエステルで構成されたA層とポリエステルで構成されたB層との少なくとも2層を有する白色ポリエステルフィルムであって、該B層は気泡を有し、該A層はルチル型酸化チタン、硫酸バリウムおよび二酸化珪素の3種類の無機粒子を含有し、該白色ポリエステルフィルムの全厚みが100μm以上500μm以下であり、かつ該A層の厚みが2μm以上16μm以下である白色ポリエステルフィルム。 A white polyester film having at least two layers of an A layer composed of polyester and a B layer composed of polyester, wherein the B layer has air bubbles, and the A layer comprises rutile titanium oxide, barium sulfate, and A white polyester film containing three types of inorganic particles of silicon dioxide, wherein the total thickness of the white polyester film is from 100 μm to 500 μm, and the thickness of the A layer is from 2 μm to 16 μm.
- 前記A層が、前記ルチル型酸化チタンを該A層の全質量に対して2質量%以上6質量%以下、前記硫酸バリウムを該A層の全質量に対して16質量%以上24質量%以下、前記二酸化珪素を該A層の全質量に対して0.5質量%以上3質量%以下含有する請求項1記載の白色ポリエステルフィルム。 In the A layer, the rutile titanium oxide is 2% by mass to 6% by mass with respect to the total mass of the A layer, and the barium sulfate is 16% by mass to 24% by mass with respect to the total mass of the A layer. The white polyester film according to claim 1, wherein the silicon dioxide is contained in an amount of 0.5% by mass to 3% by mass with respect to the total mass of the A layer.
- 前記ルチル型酸化チタンの数平均粒径が0.1μm以上1.0μm以下である請求項1または2記載の白色ポリエステルフィルム。 The white polyester film according to claim 1 or 2, wherein the rutile-type titanium oxide has a number average particle size of 0.1 µm or more and 1.0 µm or less.
- 前記硫酸バリウムの数平均粒径が0.5μm以上3.0μm以下である請求項1~3のいずれかに記載の白色ポリエステルフィルム。 The white polyester film according to any one of claims 1 to 3, wherein the barium sulfate has a number average particle size of 0.5 to 3.0 µm.
- 前記二酸化珪素の数平均粒径が2.0μm以上5.0μm以下である請求項1~4のいずれかに記載の白色ポリエステルフィルム。 The white polyester film according to any one of claims 1 to 4, wherein the number average particle diameter of the silicon dioxide is 2.0 袖 m to 5.0 袖 m.
- 前記B層が、ポリエステルと非相溶なポリマーまたは、ポリエステルと非相溶なポリマーおよび無機粒子を分散して含有する請求項1~5のいずれかに記載の白色ポリエステルフィルム。 The white polyester film according to any one of claims 1 to 5, wherein the layer B contains a polymer incompatible with polyester, or a polymer incompatible with polyester and inorganic particles dispersed therein.
- 前記A層に照度:100mW/cm2、温度:60℃、相対湿度:50%RH、照射時間:48時間の条件で紫外線を照射したときの、紫外線照射前と紫外線照射後とでの黄色味変化量:Δb値が5未満である請求項1~6のいずれかに記載の白色ポリエステルフィルム。 Yellowness before and after ultraviolet irradiation when the layer A is irradiated with ultraviolet rays under the conditions of illuminance: 100 mW / cm 2 , temperature: 60 ° C., relative humidity: 50% RH, and irradiation time: 48 hours. The white polyester film according to any one of claims 1 to 6, wherein the change: Δb value is less than 5.
- 請求項1~7のいずれかに記載の白色ポリエステルフィルムを用いた光反射板。 A light reflector using the white polyester film according to any one of claims 1 to 7.
- 請求項1~7のいずれかに記載の白色ポリエステルフィルムがそのA層面側を光源側に向けて配されている液晶ディスプレイ用バックライト。 A backlight for a liquid crystal display, wherein the white polyester film according to any one of claims 1 to 7 is disposed with its layer A surface facing the light source.
Priority Applications (3)
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CN201180010943.7A CN102782532B (en) | 2010-03-23 | 2011-02-21 | White polyester film, light-reflective plate using the same, and liquid-crystal display backlight using the same |
KR1020127022727A KR101772015B1 (en) | 2010-03-23 | 2011-02-21 | White polyester film, light-reflective plate using the same, and liquid-crystal display backlight using the same |
JP2011522311A JP5045851B2 (en) | 2010-03-23 | 2011-02-21 | White polyester film, light reflector using the same, and backlight for liquid crystal display |
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JP2010065659 | 2010-03-23 | ||
JP2010-065659 | 2010-03-23 |
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PCT/JP2011/053633 WO2011118305A1 (en) | 2010-03-23 | 2011-02-21 | White polyester film, light-reflective plate using the same, and liquid-crystal display backlight using the same |
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JP (1) | JP5045851B2 (en) |
KR (1) | KR101772015B1 (en) |
CN (1) | CN102782532B (en) |
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WO (1) | WO2011118305A1 (en) |
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WO2014021476A1 (en) * | 2012-08-03 | 2014-02-06 | 帝人デュポンフィルム株式会社 | White reflective film |
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JP2014142650A (en) * | 2014-03-05 | 2014-08-07 | Teijin Dupont Films Japan Ltd | White reflection film |
JP2014146038A (en) * | 2014-03-05 | 2014-08-14 | Teijin Dupont Films Japan Ltd | White reflection film |
CN104246545A (en) * | 2012-07-30 | 2014-12-24 | 东丽株式会社 | White polyester film for liquid crystal display |
JP2016108504A (en) * | 2014-12-10 | 2016-06-20 | 東レ株式会社 | Biaxially-oriented polyester film |
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US10475943B2 (en) * | 2015-03-20 | 2019-11-12 | Toyobo Co., Ltd. | White polyester film for a solar cell, sealing sheet for back surface of solar cell using same, and solar cell module |
CN107408595B (en) * | 2015-03-20 | 2020-03-10 | 东洋纺株式会社 | White polyester film for solar cell, solar cell back surface sealing sheet using same, and solar cell module |
Also Published As
Publication number | Publication date |
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JP5045851B2 (en) | 2012-10-10 |
CN102782532B (en) | 2015-04-15 |
TW201137384A (en) | 2011-11-01 |
KR20130018668A (en) | 2013-02-25 |
CN102782532A (en) | 2012-11-14 |
TWI495898B (en) | 2015-08-11 |
JPWO2011118305A1 (en) | 2013-07-04 |
KR101772015B1 (en) | 2017-08-28 |
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