|Número de publicación||US20070042168 A1|
|Tipo de publicación||Solicitud|
|Número de solicitud||US 10/580,399|
|Número de PCT||PCT/JP2004/017413|
|Fecha de publicación||22 Feb 2007|
|Fecha de presentación||24 Nov 2004|
|Fecha de prioridad||25 Nov 2003|
|También publicado como||CN1886259A, WO2005051654A1|
|Número de publicación||10580399, 580399, PCT/2004/17413, PCT/JP/2004/017413, PCT/JP/2004/17413, PCT/JP/4/017413, PCT/JP/4/17413, PCT/JP2004/017413, PCT/JP2004/17413, PCT/JP2004017413, PCT/JP200417413, PCT/JP4/017413, PCT/JP4/17413, PCT/JP4017413, PCT/JP417413, US 2007/0042168 A1, US 2007/042168 A1, US 20070042168 A1, US 20070042168A1, US 2007042168 A1, US 2007042168A1, US-A1-20070042168, US-A1-2007042168, US2007/0042168A1, US2007/042168A1, US20070042168 A1, US20070042168A1, US2007042168 A1, US2007042168A1|
|Inventores||Tadaaki Harada, Yuuzou Akada, Yoshimasa Sakata|
|Cesionario original||Nitto Denko Corporation|
|Exportar cita||BiBTeX, EndNote, RefMan|
|Citada por (19), Clasificaciones (25), Eventos legales (1)|
|Enlaces externos: USPTO, Cesión de USPTO, Espacenet|
The present invention relates mainly to a resin sheet suitable for use in a display device, as well as a substrate for a display device, a display device and a substrate for a solar cell, each including the resin sheet.
For liquid crystal display devices, electroluminescence display devices and the like, it is proposed to use plastic substrates in place of conventional glass substrates for progress in making displays lightweight, low-profile and high impact. Whilst substrates of the above type are required to have a low coefficient of thermal expansion, plastic substrates may pose a problem of causing misalignment when forming, for example, electrodes or color filters, due to thermal shrinkage and expansion, since plastic has a higher coefficient of linear expansion than glass.
Although those of various active matrix driving types are recently used especially in the field of liquid crystal display devices thanks to the excellent display quality compared with passive matrix driving types, the above problem is more significant in the liquid crystal display devices of the active matrix driving types because they are required to have a lower coefficient of thermal expansion than the passive matrix driving types.
Another problem associated with plastic substrates is that the mechanical strength thereof is relatively low.
In light of the above problems, there is proposed a resin sheet for a substrate that includes a cured resin layer having a glass fiber cloth-like material embedded therein by impregnating the glass fiber cloth-like material with a pre-cured resin, molding it into a sheet and curing the same, in which the glass fiber cloth-like material is formed by weaving glass fibers into cloth (Patent documents 1, 2 referred below).
Patent Document 1: Official Gazette of Japanese Patent Application Laid-open No. 2003-50384
Patent Document 2: Official Gazette of Japanese Patent Application Laid-open No. Hei-11-2812
Problems to be Solved by the Invention
However, in a resin sheet for a substrate manufactured by embedding a glass fiber cloth-like material in a cured resin layer, the cured resin layer is resultingly made up of two components, namely glass and resin, and therefore light transmitted therethrough may be diffused causing undesirable effects on light transparency.
The thus arranged resin sheet is easy to have an irregular surface due to the shape of the glass fiber cloth-like material, which may cause undesirable effects on light transparency.
Accordingly, it is an object of the present invention to provide a resin sheet that achieves improvement in lightweight, low-profile and high impact characteristics, suppresses thermal shrinkage and expansion and is excellent in light transparency so as to prevent the display quality or the like of a display device from being deteriorated, as well as providing a substrate for a display device, a display device and a substrate for a solar cell, each having the aforesaid resin sheet.
Means of Solving the Problems
In consideration of the above problems, according to the present invention, there is provided a resin sheet, characterized in that it includes a cured resin layer containing a glass fiber cloth-like material and an overcoat layer laminated on the cured resin layer to have a surface roughness Rt of 200 nm or less, and is structured to have a haze value of 10% or lower.
In the present invention, a haze value maybe measured according to, for example, JIS K 7136, and is measured specifically by using a commercially available hazemeter (e.g., “HM-150”, trade name; manufactured by Murakami Color Research Laboratory).
Effects of the Invention
With the resin sheet of the present invention, the cured resin layer containing the glass fiber cloth-like material as provided can realize lightweight, low-profile, and improvement in impact resistance, and suppress thermal shrinkage and expansion. Therefore, it is possible to prevent misalignment of an electrode, a color filter or the like as mentioned above when used as a liquid crystal cell substrate for forming a liquid crystal panel.
In the resin sheet of the present invention, an overcoat layer is laminated on the cured resin layer to have a surface roughness of 200 nm or less, thereby eliminating unevenness due to the glass fiber cloth-like material; and the resin sheet is structured to have a haze value of 10% or lower, thereby achieving reduced light diffusion and thus providing a resin sheet that is remarkably excellent in light transparency. Therefore, when used as a liquid crystal cell substrate, a substrate for an electroluminescence display device or the like, the display quality of a display device becomes excellent. Furthermore, a substrate for a solar cell including the resin sheet may contribute to the improvement in power generating efficiency of the solar cell.
1: cured resin layer
2: glass fiber cloth-like material
3: overcoat layer
4: gas barrier layer
5: hard-coat layer
10: resin sheet
As illustrated in
Examples of the glass fiber cloth-like material include fabric, non-woven fabric and knitted fabric; and specifically known commercially available products such as glass non-woven fabric, roving cloth, chopped strand mat and unidirectional woven roving (cord fabric), as well as commonly used glass cloth produced by weaving yarns can be used.
The glass fiber cloth-like material has a density preferably in a range from 10 to 500 g/m2, more preferably in a range from 20 to 350 g/m2 and still more preferably in a range from 30 to 250 g/m2. The glass fiber has a filament diameter of preferably 3 to 15 μm, more preferably 5 to 13 μm, and still more preferably 5 to 10 μm. As a material of the glass fiber, soda glass, borosilicate glass, no alkali glass, etc., are used; and of them, no alkali glass is preferable since alkali components may cause undesirable effects on a TFT or the like.
The glass fiber cloth-like material has a thickness of preferably 10 to 500 μm, more preferably 15 to 350 μm and still more preferably 30 to 250 μm.
As a resin forming a cured resin layer, thermosetting resins or UV curing resins, such as polyethersulfone, polycarbonate, epoxy resins, acryl resins or various optical polyolefin resins may be used. Of them, epoxy resins are preferably used since they are excellent in surface smoothness and color hue.
The cured resin layer has a thickness of preferably 20 to 800 μm. With a thickness of less than 20 μm, poor strength or stiffness may be caused, and with a thickness of more than 800 μm, advantages of a resin sheet such as low profile and light weight may be decreased.
As an epoxy resin for forming a cured resin layer, it is possible to use hitherto known epoxy resins, which include bisphenol types such as bisphenol A type, bisphenol F type, bisphenol S type, and hydrogenated epoxies derived from these; novolak types such as phenol novolak type and cresol novolak type; nitrogen-containing cyclic types such as triglycidyl isocyanurate type and hydantoin type; alicyclic types; aliphatic types; aromatic types such as naphthalene type; low-water-absorption types such as glycidyl ether type and biphenyl type; dicyclo types such as dicyclopentadiene type; ester types; etherester types; and modifications of these.
Of these epoxy resins, preferred epoxy resins from the standpoints of unsusceptibility to discoloration, etc., are bisphenol A type epoxy resin, alicyclic type epoxy resin and triglycidyl isocyanulate type epoxy resin. These epoxy resins may be used alone or in combination of two or more thereof.
Examples of the dicyclopentadiene type epoxy resin (an epoxy resin having the skeleton of dicyclopentadiene) include epoxy resins respectively represented by the following formula (1), (2). In the formula (2), n represents an integer of 1 to 3.
By the use of the epoxy resin represented by the formula (1) or (2), it is possible to control the thicknesswise retardation of a resin sheet to a small value. When the thicknesswise retardation is small, it is possible to suppress light leakage in an oblique direction in a black display mode when the laminated film is used in a liquid crystal display device. Thus, the display characteristics are more improved.
From the standpoint of improving, for example, the flexibility or strength of a resin sheet to be formed, the epoxy resin preferably has an epoxy equivalent of 100 to 1000 (g/eq) and a softening point of 120° C. or below. The epoxy resin preferably remains in a liquid state at ordinal temperature (e.g., 5 to 35° C.). For forming a resin sheet, it is preferable to use a two-component epoxy resin that remains in a liquid state at a temperature equal to or lower than the temperature at which the coating is carried out, or particularly at ordinal temperature, since it is excellent in spreading property and coatability.
The cured resin layer may be mixed with various types of additives other than resins, according to needs and circumstances.
Examples of the additives include curing agents, curing accelerators, age resistors, modifying agents, surfactants, colorants, pigments, discoloration inhibitors and UV absorbers.
Examples of the curing agent include without limitation organic acid compounds such as tetrahydrophthalic acid, methyltetrahydrophthalic acid, hexahydrophthalic acid and methylhexahydrophthalic acid, and amine compounds such as ethylenediamine, propylenediamine, diethylenetriamine, triethylenetetramine, amine adducts thereof, methaphenylenediamine, diaminodiphenylmethane and diaminodiphenylsulfone. These may be used alone or in combination of two or more thereof.
Further examples of the curing agent include amide compounds such as dicyandiamide and polyamide, hydrazide compounds such as dihydrazide, imidazole compounds such as methylimidazole, 2-ethyl-4-methylimidazole, ethylimidazole, isopropylimidazole, 2,4-dimethylimidazole, phenylimidazole, undecylimidazole, heptadecylimidazole and 2-phenyl-4-methylimidazole, imidazoline compounds such as methylimidazoline, 2-ethyl-4-methylimidazoline, ethylimidazoline, isopropylimidazoline, 2,4-dimethylimidazoline, phenylimidazoline, undecylimidazoline, heptadecylimidazoline and 2-phenyl-4-methylimidazoline, phenol compounds, urea compounds and polysulfide compounds.
In addition, acid anhydrides and the like may be used as the curing agent, and these acid anhydrides are preferably used from the standpoints of, for example, discoloration inhibiting characteristics. Examples of these acid anhydrides include phthalic anhydride, maleic anhydride, trimellitic anhydride, pyromellitic anhydride, nadic anhydride, glutaric anhydride, tetrahydrophthalic anhydride, methyltetrahydrophthalic anhydride, hexahydrophthalic anhydride, methylhexahydrophthalic anhydride, methylnadic anhydride, dodecenylsuccinic anhydride, dichlorosuccinic anhydride, benzophenonetetracarboxylic anhydride and chlorendic anhydride. Of these acid anhydrides, it is preferable to use colorless or pale yellow acid anhydride curing agents having a molecular weight of from about 140 to about 200, such as phthalic anhydride, tetrahydrophthalic anhydride, hexahydrophthalic anhydride, methylhexahydrophthalic anhydride or methylnadic anhydride.
When an epoxy resin is used as a resin that forms the cured resin layer, no limitation is intended on the amount of the curing agent to be added in the epoxy resin; but when an acid anhydride curing agent is used as a curing agent, an acid anhydride is added in an amount of, for example, preferably from 0.5 to 1.5 equivalents, and more preferably from 0.7 to 1.2 equivalents, per equivalent of epoxy group in the epoxy resin. With the acid anhydride curing agent added in an amount of 0.5 equivalents or more, it is possible to make the color tint after curing more significant, and with being 1.5 equivalents or less, satisfactory moisture resistance can be kept. In a case where a different curing agent is used, or two or more types of the curing agents are used, it is possible to mix them according to the aforesaid equivalent ratio.
Examples of the curing accelerator include without limitation tertiary amines, imidazoles, quaternary ammonium salts, quaternary phosphonium salts, organic metal salts, phosphorus compounds and urea compounds, and of them, tertiary amines, imidazoles and quaternary phosphonium salts are preferable. These curing accelerators may be used alone or in combination of two or more thereof.
The amount of the curing accelerator to be added in the cured resin layer is not limited to a specific amount, but may be determined depending on the type of the resin or the like. For example, when an epoxy resin is used, the curing accelerator is added in an amount of preferably from 0.05 to 7.0 parts by weight, and more preferably from 0.2 to 3.0 parts by weight, per 100 parts by weight of the epoxy resin. With the curing accelerator added in an amount of 0.05 parts by weight or more, satisfactory curing acceleration effect can be produced, and when in an amount of 7.0 parts by weight or less, it is possible to make the color tint after curing significant.
Examples of the age resistor include without limitation phenol compounds, amine compounds, organic sulphur compounds, phosphine compounds and other hitherto known compounds.
Examples of the modifying agent include without limitation glycols, silicones, alcohols and other hitherto known compounds.
Examples of the surfactant include various types of surfactants such as silicone, acrylic or fluorinated surfactants. Of them, silicone surfactant is preferable. These surfactants are added to smoothen the surface of a resin sheet when the resin sheet is to be formed, for example, by curing a resin in contact with air by a flow-casting method or the like.
In a resin sheet of the present invention, the absolute value of the difference in refractive index between a resin, which forms a cured resin layer, and a glass fiber cloth-like material is from 0 to 0.01, preferably from 0 to 0.008, and more preferably from 0 to 0.006. The absolute value of the difference in refractive index is preferably equal to or less than 0.01, since interface scattering between the glass fiber cloth-like material and the resin, which forms a cured resin layer, in the cured resin layer is suppressed, thereby enabling decreasing the haze and hence satisfactorily maintaining the original transparency of the cured resin layer.
The refractive index may be measured by use of an Abbe refractometer at 25° C. and 589 nm.
Meanwhile, the overcoat layer 3 of the resin sheet 10 of the present invention is laminated on the cured resin layer 1 to have a surface roughness Rt of 200 μm or less, and preferably laminated on the cured resin layer 1 to have a surface roughness Rt of 100 μm or less. As illustrated in
The overcoat layer(s) as provided makes it possible to eliminate unevenness due to, for example, the shape of a glass fiber cloth-like material and the difference in shrinkage ratio between a glass fiber cloth-like material and a resin, and hence produce a resin sheet that is excellent in surface smoothness and transparency.
In the present invention, the “surface roughness Rt” represents a difference between a maximum value and a minimum value, which are obtained by measurement using a stylus type surface roughness meter (e.g., “P-11”, trade name; manufactured by KLA-Tencor Ltd.) under a condition of a long wavelength cut-off of 800 μm, a short wavelength cut-off of 250 μm, and an evaluation length of 10 mm.
From the standpoint of producing excellent surface smoothness and preventing gap-unevenness in a display device and thus making the image of the image display more clear, the overcoat layer has a thickness of preferably 5 to 70 μm and more preferably 10 to 30 μm.
In a case where overcoat layers are laminated on both the front and back sides of the cured resin layer, the overcoat layers on the front and back sides each have such a thickness as to have a thickness difference of preferably 10 μm or less therebetween from the standpoint of preventing curling of a resin sheet.
As a resin for forming the overcoat layer, although no limitation is intended, a resin that is cured at room temperature is preferably used since there is no shrinkage after being cured. Examples of a resin that is cured at room temperature include UV curing resins using cationic photo-initiator. Of them, a mixture of an oxetane resin and an epoxy resin is preferably used since it is excellent in chemical resistance.
From the standpoint of improving the transparency, the refractive index difference of a resin of the overcoat layer relative to the resin of the cured resin layer is preferably 0.03 or less.
According to needs and circumstances, antioxidant, UV absorber, colorant, pigment, inorganic filler, surfactant or any other know additive may be added to the overcoat layer. When adding inorganic filler, nanoparticles (particle size of 100 nm or less) are preferable since they do not cause undesirable effects on the transparency of a resin sheet.
A resin sheet of the present invention is preferably structured so as to have a coefficient of linear expansion being equal to or less than 3.00×10−5/° C. at a temperature from 25° C. to 160° C., by having a glass fiber cloth-like material contained therein, as mentioned above.
When the coefficient of linear expansion is equal to or less than 3.00×10−5/° C. for a laminated film of the present invention, which is used as, for example, a liquid crystal cell substrate on which a color filter, an electrode, etc., are formed, it is possible to satisfactorily suppress misalignment or the like therebetween due to thermal expansion, and hence more easily form a color filter, etc. The coefficient of linear expansion is more preferably equal to or less than 2.00×10−5/° C., and still more preferably equal to or less than 1.5×10−5/° C.
The coefficient of linear expansion is determined by obtaining a TMA measured value by the TMA method specified in JIS K 7197 and substituting it into the following expression. In the following expression, ΔIs(T1) and ΔIs(T2) represent TMA measured values (μm) respectively obtained at a temperature T1(° C.) and a temperature T2(° C.), at which the measurement is carried out, and L0 represents a length (mm) of an object to be measured, at a room temperature of 23° C.
Coefficient of linear expansion=[1/(L 0×103)]·[(ΔIs(T 2)−ΔIs(T1))/(T 2 −T 1)]
The resin sheet 10 of the present invention has a haze value of 10% or lower, and preferably 8% or lower and more preferably 5% or lower from the standpoint of producing more excellent transparency of the resin sheet and further improving the display quality of a display device.
A resin sheet of the present invention is preferably structured to have a light transmittance of 88% or higher by having the refractive index difference between the cured resin layer and the glass fiber cloth-like material being 0.01 or less.
When the light transmittance is 88% or higher, it is possible to provide more crisp characters or images in various types of image display devices, and thus achieving more excellent display quality, when those image display devices each are assembled by using a resin sheet of the present invention as a liquid crystal cell substrate, a substrate for an electroluminescence display device, or the like.
The light transmittance may be determined by measuring a total transmittance of light rays with a wavelength of 550 nm, using a high-speed spectrophotometer.
A method of manufacturing a resin sheet of the present invention is not necessarily limited to a specific method.
The cured resin layer may be manufactured by any proper technique, provided that a glass fiber cloth-like material is impregnated with a resin and curing is made after that such as by a cast molding technique, a flow-casting technique, an impregnation technique, a coating technique or the like.
The overcoat layer may be formed by any proper technique, such as by coating a resin, which forms the overcoat layer, on the cured resin layer by flow-casting by using a die coater or the like, and then curing the resin.
A resin sheet of the present invention is preferably a laminated body that further includes at least one of a hard-coat layer, which is harder than the cured resin layer, and a gas barrier layer, which is more excellent in gas barrier properties than the cured resin layer. Particularly, as illustrated in
In a case where both a hard-coat layer and a gas barrier layer are laminated, the order, in which they are laminated, is not necessarily limited to a specific order; but it is preferable to laminate first a gas barrier layer and then a hard-coat layer onto the cured resin layer. Particularly, the hard-coat layer is preferably laminated as an outermost layer since it is excellent in impact resistance, chemical resistance, etc.
Examples of a material for forming the hard-coat layer include without limitation urethane resins, acrylic resins, polyester resins, polyvinyl alcohol resins such as polyvinyl alcohol, ethylene vinyl alcohol copolymer, vinyl chloride resins and vinylidene chloride resins. For example, it is possible to use polyarylate resins, sulfone resins, amide resins, imide resins, polyether sulfone resins, polyether imide resins, polycarbonate resins, silicone resins, fluororesins, polyolefin resins, styrene resins, vinylpyrrolidone resins, cellulose resins, acrylonintrile resins, etc. Of them, urethane resins are preferable, and urethane acrylate is more preferable. These resins may be used alone or in combination of two or more as a blended resin.
Although no limitation is intended, the thickness of the hard-coat layer is, for example, in a range from 0.1 to 50 μm, preferably from 0.5 to 8 μm, and more preferably from 2 to 5 μm, from the standpoints of ease to remove and prevention of occurrence of cracking due to the removal, when manufacturing.
The gas barrier layer is categorized into, for example, an organic gas barrier layer and an inorganic gas barrier layer. Examples of a material for forming the organic gas barrier layer include without limitation polyvinyl alcohol and a partially saponified product thereof, vinyl alcohol polymers such as ethylene vinyl alcohol copolymer, materials with low oxygen-permeability such as polyacrylonitrile, and polyvinylidene chloride. Of these materials, vinyl alcohol polymers are particularly preferably used from the standpoint of their high gas barrier properties.
From the standpoints of, for example, functionality in terms of transparency, prevention of coloration, gas barrier properties and the like, as well as reduction in thickness, flexibility of a resulting resin sheet and the like, the thickness of the organic gas barrier layer is, preferably 10 μm or smaller, more preferably from 2 to 10 μm, and still more preferably from 3 to 5 μm. In the resin sheet, with the thickness being 10 μm or smaller, a lower yellow color index (YI value) may be maintained, and with the thickness being 2 μm or greater, satisfactory gas barrier performance can be maintained.
Meanwhile, as a material for forming an inorganic gas barrier layer, for example, transparent materials such as silicon oxides, magnesium oxides, aluminum oxides, zinc oxides and the like may be used. Of these materials, silicon oxides and silicon nitrides are preferably used from the standpoints of, for example, their excellent gas barrier properties, adhesion to the substrate layer and the like.
Preferably, the silicon oxides have, for example, a ratio of the number of oxygen atoms to the number of silicon atoms of 1.5 to 2.0 for the following reason. That is, with this ratio, the inorganic gas barrier layer is improved further in terms of, for example, gas barrier properties, transparency, surface smoothness, bending properties, membrane stress, cost, and the like. In the silicon oxides, the maximum value of the ratio of the number of oxygen atoms to the number of silicon atoms is 2.0.
The silicon oxides preferably have a ratio (Si:N) of the number of nitrogen atoms (N) to the number of silicon atoms (Si) of 1:1 to 3:4.
Although no limitation is intended, the inorganic gas barrier layer has a thickness preferably in a range of, for example, from 5 to 200 nm. With the thickness being 5 nm or greater, for example, more excellent gas barrier properties can be obtained, and with the thickness being 200 nm or smaller, the inorganic gas barrier layer is improved also in terms of transparency, bending properties, membrane stress, and cost.
When a resin sheet of the present invention is a laminated body, its thickness, which varies depending on the number of layers laminated, is preferably for example in the range from 30 to 800 μm. The resin sheet having such a thickness fully exerts advantages of the resin sheet, namely excellent strength and stiffness, low-profile, lightweight, etc.
The method of laminating a hard-coat layer, a gas barrier layer, etc., is not necessarily limited to a specific method, and they may be laminated by any appropriate method on a cured resin layer or an overcoat layer formed on the cured resin layer.
A resin sheet of the present invention may be used for various purposes, and may be appropriately used for a liquid crystal cell substrate, a substrate for an electroluminescence display device and a substrate for a solar cell.
A liquid crystal display device is generally made up of a polarizing plate, a liquid crystal cell and a reflection plate or a backlight, as well as any elements such as other optical parts appropriately assembled according to needs and circumstances, and a driving circuit incorporated thereinto. A liquid crystal display device of the present invention may be made up of those elements in the same manner as a conventional device, except that a liquid crystal cell is formed by using a liquid crystal cell substrate that employs the aforesaid resin sheet.
Therefore, it is possible to combine the aforesaid resin sheet with an appropriate optical part such as a diffusion plate, an antiglare layer, an antireflection film, a protection layer or a protection plate provided on a polarizing plate on a visible side, or a compensating retardation plate provided between a liquid crystal cell and a polarizing plate on a visible side.
An electroluminescence display device has a luminescence element that is generally made up of a transparent electrode, an organic luminant layer containing a luminant (an organic electroluminescence ruminant) and a metal electrode laminated in a certain order on a transparent substrate. An electroluminescence display device of the present invention may be made up of those elements in the same manner as a conventional device, except that the aforesaid resin sheet is used as the transparent substrate.
The present invention will be described by citing the following examples, which are not intended to limit the present invention.
An epoxy resin liquid was prepared by stirring and mixing: 35.9 parts by weight (hereinafter referred only to parts) of 3,4-epoxycyclohexylmethyl-3,4-epoxycyclohexane carboxylate represented by the following formula (3) and 10.1 parts of a dicyclopentadiene type epoxy resin (“EXA-7230”, trade name (epoxy equivalent of 259); manufactured by Dainippon Ink And Chemicals, Incorporated) represented by the following formula (4); as a curing agent, 52.9 parts of methylnadic anhydride; and as a curing accelerator, 1.1 parts of tetra-n-butylphosphonium o,o-diethylphosphorodithioate represented by the following formula (5).
Then, the aforesaid epoxy resin liquid was impregnated into a glass fiber cloth-like material (“NEA2116F S136”, trade name; manufactured by Nitto Boseki Co., Ltd., a refractive index of 1.513, a thickness of 90 μm), and left to stand for 60 minutes under a condition of a reduced pressure (200 Pa).
Then, a hard-coat layer having a thickness of 2 μm was formed by flow-casting a toluene solution having 17 weight % of urethane acrylate represented by the following formula (6) from a die onto an endless belt of stainless steel at a running speed of 0.3 m/min., air-drying it to volatilize toluene and curing the remaining by using a UV curing device. Subsequently, the glass fiber cloth-like material with the epoxy resin liquid impregnated thereinto was laminated thereon, and was cured by using a heating device. Thus, a laminate with the hard-coat layer and the cured resin layer laminated together, having a thickness of 100 μm, was obtained. According to the measurement, a portion of the cured resin layer other than the glass fiber cloth-like material had a refractive index of 1.522 and had a refractive index difference of 0.009 with respect to the glass fiber cloth-like material.
Then, a resin solution for forming an overcoat layer was prepared by uniformly mixing: 91 parts of an oxetane resin (“ARON OXETANE OXT-221”, trade name; manufactured by Toagosei Co., Ltd.); 4.8 parts of 3,4-epoxycyclohexylmethyl-3,4-epoxycyclohexane carboxylate represented by the formula (3); and 4.3 parts of a photocationic initiator (“ADEKA OPTOMER SP-170”, trade name; manufactured by Asahi Denka Co., Ltd.).
Then, the laminate of the hard-coat layer and the cured resin layer was removed from the endless belt and left to stand for 1 hour at 200° C. on a glass plate in an atmosphere with an oxygen concentration of 0.1%, which atmosphere being achieved by nitrogen substitution, and then post-curing was done. Then, a resin sheet with an overcoat layer formed on its surface layer was prepared by coating a resin solution for forming the overcoat layer on the cured resin layer to have a thickness of 30 μm by flow-casting coating by a continuous die coater (manufactured by Chugai Ro Co., Ltd.), then placing it between glass plates each having a thickness of 5 mm, radiating UV light and thereby curing the resin. The UV light exposure amount was 1000 mJ/cm2.
A resin sheet was prepared in the same manner as in Example 1 except that, of the resins for forming an overcoat layer, the other oxetane resin (“ARON OXETANE OXT-121”, trade name; manufactured by Toagosei Co., Ltd.) was used as an oxetane resin.
A resin sheet was prepared in the same manner as in Example 1 except that an overcoat layer was not formed.
A resin sheet was prepared in the same manner as in Example 1 except that a glass cloth (manufactured by Nitto Boseki Co., Ltd.) having a refractive index of 1.558 and a thickness of 100 μm was used as a glass fiber cloth-like material, and an overcoat layer was not formed. In a cured resin layer, the refractive index difference between a portion other than the glass fiber cloth-like material and the glass fiber cloth-like material was 0.036.
For the resin sheets of Examples and Comparative Examples, measurement was made for each of the coefficient of linear expansion, bending properties, light transmittance and surface roughness. The measurements each were made as follows:
Coefficient of Linear Expansion (/° C.): Using a TMA/SS150C, trade name (manufactured by Seiko Instruments Inc.), TMA values (μm) at temperatures of 25° C. and 160° C. were respectively measured, and determination was performed.
Bending Properties: Each of the resin sheets was wound around a steel mast having a diameter of 35 mm, and a visual observation was performed to check if a crack had been caused.
Light Transmittance: A light transmittance of λ=550 nm was measured using a high-speed spectrophotometer (“CMS-500”, trade name; manufactured by Murakami Color Research Laboratory, using a halogen lamp).
Surface Roughness: A surface roughness (difference between a maximum value and a minimum value) was measured using a stylus type surface roughness meter (“P-11”, trade name; manufactured by KLA-Tencor Ltd.) under a condition of a long wavelength cut-off of 800 μm, a short wavelength cut-off of 250 μm, and an evaluation length of 10 mm.
Haze Value: With respect to each of the resin sheets, a haze value was measured using a hazemeter (“HM-150”, trade name; manufactured by Murakami Color Research Laboratory).
The results are shown in Table 1.
TABLE 1 Comparative Comparative Example 1 Example 2 Example 1 Example 2 Refractive Index 0.009 0.009 0.009 0.036 Difference Overcoat Layer Presence Presence Nil Nil Surface Roughness 110 nm 130 nm 500 nm 500 nm (Rt) Coefficient of Linear 1.8 × 10−5/° C. 1.9 × 10−5/° C. 1.8 × 10−5/° C. 1.8 × 10−5/° C. Expansion Bending Properties No Crack No Crack No Crack No Crack Light 88% 88% 89% 86% Transmittance Haze Value 5% 5% 5% 75%
As shown in Table 1, the resin sheets of Examples 1 and 2 each had a low coefficient of linear expansion and were excellent in light transmittance and surface smoothness. Also, the bending properties were excellent. On the other hand, the resin sheet of Comparative Example 1 had a poor surface smoothness compared with those of the Examples, although was excellent in coefficient of linear expansion, light transmittance and bending properties likewise those of the Examples. The resin sheet of Comparative Example 2 had a poor surface smoothness compared with those of the Examples and a haze value of 75% and caused turbidity or cloudiness, although was excellent in coefficient of linear expansion, light transmittance and bending properties likewise those of the Examples.
A transmissive liquid crystal display device was assembled by using the resin sheet of each of the Examples and the Comparative Examples, and there were no problems such as misalignment, break or the like in forming an oriented film, patterning a color filter layer and forming a liquid crystal cell.
Meanwhile, in a transmissive liquid crystal display device using the resin sheet of Comparative Example 1, deterioration in image quality, which is seemed to be due to a specific surface smoothness of the resin sheet was confirmed.
A transmissive liquid crystal display device using the resin sheet of Comparative Example 2 did not fully carry out the function as a display device due to turbidity or cloudiness on the display.
|Patente citante||Fecha de presentación||Fecha de publicación||Solicitante||Título|
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|Clasificación de EE.UU.||428/292.1, 428/917, 428/1.6, 257/E31.041|
|Clasificación internacional||B32B5/28, H05B33/14, G09F9/35, B32B27/04, B32B27/12, G09F9/30, H01L51/50, H01L27/32, H01L31/0392, D04H13/00, G02F1/1333, H05B33/02|
|Clasificación cooperativa||Y10T428/249924, Y10T428/1086, B32B27/12, Y02E10/50, H01L31/0392, G02F1/133305|
|Clasificación europea||G02F1/1333B, B32B27/12, H01L31/0392|
|24 May 2006||AS||Assignment|
Owner name: NITTO DENKO CORPORATION, JAPAN
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:HARADA, TADAAKI;AKADA, YUUZOU;SAKATA, YOSHIMASA;REEL/FRAME:017939/0126
Effective date: 20060510