Patent Application
20120128985
The present invention relates to a laminated polyester film, and more particularly, to a laminated polyester film which can be suitably used as various optical members which are required to have good adhesion to a light diffusion layer, an anti-sticking layer or the like, for example, in a backlight unit of liquid crystal displays, etc.
In recent years, liquid crystal displays have been extensively used as a display device for TVs, personal computers, digital cameras, cellular phones, etc. Since these liquid crystal displays have no light-emitting function by themselves, those liquid crystal displays of such a type in which light is irradiated from a backside thereof using a backlight have now come to dominate.
As the backlight type liquid crystal displays, there are known those having a so-called edge light type structure or a so-called direct backlight type structure. With the recent tendency toward reduction in thickness of liquid crystal displays, the edge light type liquid crystal displays have been more frequently employed. The edge light type liquid crystal displays are generally constructed from a reflection sheet, a light guide plate, a light diffusion sheet and a prism sheet which are successively laminated in this order. The flow of light through such edge light type liquid crystal displays is designed such that the light entered from the backlight into the light guide plate is reflected on the reflection sheet and then emitted from the surface of the light guide plate. The light emitted from the light guide plate is entered into the light diffusion sheet, diffused therein and then emitted therefrom. The light emitted from the light diffusion sheet is entered into the prism sheet disposed next to the light diffusion sheet in which the light is converged in the normal direction and emitted therefrom toward the liquid crystal layer.
The light diffusion sheet used in the above construction serves for uniformly diffusing the light penetrated therethrough in the multiple directions, and is required to have a large light diffusion property and a high light transmittance. As the light diffusion sheet, there are known those having an irregular sheet surface, i.e., a so-called embossed surface which is formed by subjecting the sheet to heating and pressing treatments upon finishing, and those in which a light diffusion layer formed from a transparent resin comprising particles is coated on a transparent base film. In addition, there has been proposed such a light diffusion sheet in which an anti-sticking layer comprising a binder and a small amount of beads is formed on the surface of a transparent base film which is opposite to its surface provided with the light diffusion layer, in order to prevent sticking (partial adhesion) between the light diffusion sheet and the light guide plate, and the like (Patent Documents 1 to 3).
As the transparent base film used for forming the light diffusion sheet, there has been generally used a polyester film in view of a transparency and mechanical properties thereof. In general, an easy-bonding coating layer may be further provided as an intermediate layer between the polyester film as a base material and the light diffusion layer or the anti-sticking layer in order to enhance adhesion therebetween. As the coating layer having an easy-bonding property, there are known, for example, those coating layers produced from polyester resins, acrylic resins, urethane resins or the like (Patent Documents 4 and 5).
In recent years, in the field of liquid crystal displays, there is an increasing demand for displays having a larger image screen and a higher image quality. In addition, with the considerable reduction in price of the liquid crystal displays, it has been required to achieve considerable cost-down in processing steps for a light diffusion layer, an anti-sticking layer, etc. For this reason, there tends to occur a rapid change in construction of the light diffusion layer, the anti-sticking layer, etc., so that it has been required to provide polyester films having an easy-bonding property which can exhibit good adhesion to these various layers.
The present invention has been accomplished to solve the above conventional problems. An object of the present invention is to provide a laminated polyester film which exhibits an excellent adhesion property to various layers such as a light diffusion layer and an anti-sticking layer, and can be suitably used, for example, in a backlight unit of liquid crystal displays, etc.
As a result of the present inventors' earnest study in view of the above problems, it has been found that these problems can be readily solved by using a laminated polyester film having a specific structure. The present invention has been attained on the basis of this finding.
That is, in an aspect of the present invention, there is provided a laminated polyester film comprising a polyester film and a coating layer formed on at least one surface of the polyester film, which coating layer is produced by applying a coating solution comprising an acrylic resin, an epoxy compound and an oxazoline compound thereonto.
In accordance with the present invention, there can be provided a laminated polyester film which is excellent in adhesion to a light diffusion layer, an anti-sticking layer and the like when these layers are formed thereon. Therefore, the present invention has a high industrial value.
The present invention is described in more detail below.
The polyester film constituting the laminated polyester film of the present invention may have either a single layer structure or a multilayer structure. Unless departing from the scope of the present invention, the polyester film may have not only a two or three layer structure but also a four or more multilayer structure, and the layer structure of the polyester film is not particularly limited thereto.
The polyester used in the present invention may be either a homopolyester or a copolyester. The homopolyester is preferably obtained by polycondensing an aromatic dicarboxylic acid and an aliphatic glycol. Examples of the aromatic dicarboxylic acid include terephthalic acid and 2,6-naphthalenedicarboxylic acid. Examples of the aliphatic glycol include ethylene glycol, diethylene glycol and 1,4-cyclohexanedimethanol. Typical examples of the polyester include polyethylene terephthalate or the like. On the other hand, as a dicarboxylic acid component of the copolyester, there may be mentioned at least one compound selected from the group consisting of isophthalic acid, phthalic acid, terephthalic acid, 2,6-naphthalenedicarboxylic acid, adipic acid, sebacic acid and oxycarboxylic acids (such as, for example, p-oxybenzoic acid). As a glycol component of the copolyester, there may be mentioned at least one compound selected from the group consisting of ethylene glycol, diethylene glycol, propylene glycol, butanediol, 4-cyclohexanedimethanol and neopentyl glycol.
The polyester film used in the present invention may also comprise an ultraviolet absorber in order to prevent deterioration of liquid crystals and the like used in liquid crystal displays by irradiation with ultraviolet rays. The ultraviolet absorber is not particularly limited as long as it is a compound having a capability of absorbing an ultraviolet ray and can withstand heat applied during a process for producing the polyester film.
As the ultraviolet absorber, there are generally known an organic ultraviolet absorber and an inorganic ultraviolet absorber. In view of a good transparency, among these ultraviolet absorbers, the organic ultraviolet absorber is preferred. Examples of the organic ultraviolet absorber include, but are not particularly limited to, cyclic iminoester-based ultraviolet absorbers, benzotriazole-based ultraviolet absorbers and benzophenone-based ultraviolet absorbers. Among these organic ultraviolet absorbers, cyclic iminoester-based ultraviolet absorbers and benzotriazole-based ultraviolet absorbers are preferred in view of a good durability. These ultraviolet absorbers may be used in combination of any two or more thereof.
For the purpose of imparting an easy-slipping property to the film and preventing occurrence of flaws in the film during the respective steps, particles are preferably compounded in the polyester layer in the film of the present invention. The kinds of particles to be compounded in the polyester layer are not particularly limited as long as the particles are capable of imparting a good easy-slipping property to the film. Specific examples of the particles include particles of silica, calcium carbonate, magnesium carbonate, barium carbonate, calcium sulfate, calcium phosphate, magnesium phosphate, kaolin, aluminum oxide, titanium oxide, etc. In addition, there may also be used heat-resistant organic particles as described in Japanese Patent Publication (KOKOKU) No. 59-5216 (1984), Japanese Patent Application Laid-Open (KOKAI) No. 59-217755 (1984) or the like. Examples of the other heat-resistant organic particles include particles of thermosetting urea resins, thermosetting phenol resins, thermosetting epoxy resins, benzoguanamine resins, etc. Further, there may also be used deposited particles obtained by precipitating and finely dispersing a part of metal compounds such as a catalyst during the process for production of the polyester.
On the other hand, the shape of the particles used in the polyester layer is also not particularly limited, and may be any of a spherical shape, a massive shape, a bar shape, a flat shape, etc. Further, the hardness, specific gravity, color and the like of the particles are also not particularly limited. These particles may be used in combination of any two or more kinds thereof, if required.
The average particle diameter of the particles used in the polyester layer is usually in the range of 0.01 to 3 μm and preferably 0.1 to 2 μm. When the average particle diameter of the particles is less than 0.01 μm, the particles may fail to impart a sufficient easy-slipping property to the polyester layer, or tend to be aggregated together and therefore exhibit a poor dispersibility, which tends to result in deterioration in transparency of the resulting film. On the other hand, when the average particle diameter of the particles is more than 3 μm, the surface roughness of the obtained film tends to be too coarse, so that there tend to arise various problems when forming the light diffusion layer, the anti-sticking layer, etc., thereon in the subsequent steps.
The content of the particles in the polyester layer is usually in the range of 0.001 to 5% by weight and preferably 0.005 to 3% by weight. When the content of the particles in the polyester layer is less than 0.001% by weight, the resulting film tends to be insufficient in easy-slipping property. On the other hand, when the content of the particles in the polyester layer is more than 5% by weight, the resulting film tends to be insufficient in transparency.
The method of adding the particles into the polyester layer is not particularly limited, and any conventionally known methods can be suitably used therefor. For example, the particles may be added at any optional stages in the process for production of the polyester constituting the respective layers of the film. The particles are preferably added to the polyester after completion of an esterification reaction or a transesterification reaction thereof.
In addition, there may also be used the method of blending a slurry of the particles prepared by dispersing the particles in ethylene glycol or water with the raw polyester material using a vented kneading extruder, the method of blending the dried particles with the raw polyester material using a kneading extruder, or the like.
Meanwhile, the polyester film used in the present invention may also comprise, in addition to the above particles, known additives such as an antioxidant, an antistatic agent, a thermal stabilizer, a lubricant, a dye, a pigment, etc., if required.
The thickness of the polyester film used in the present invention is not particularly limited as long as it lies within any suitable range capable of forming a film shape, and is usually in the range of 10 to 350 μm and preferably 50 to 250 μm.
Next, an example of the process of producing the polyester film used in the present invention is more specifically explained, although not particularly limited thereto. That is, in the production process, there is preferably used such a method in which the above-mentioned raw polyester material is extruded from a die in the form of a molten sheet, and the molten sheet is cooled and solidified on a cooling roll to obtain an unstretched sheet. In this case, in order to enhance a flatness of the sheet, it is preferred to enhance adhesion between the sheet and a rotary cooling drum. For this purpose, an electrostatic adhesion method and/or a liquid coating adhesion method are preferably used. Next, the thus obtained unstretched sheet is biaxially stretched. In such a case, the unstretched sheet is first stretched in one direction thereof using a roll-type or tenter-type stretching machine. The stretching temperature is usually 70 to 120° C. and preferably 80 to 110° C., and the stretch ratio is usually 2.5 to 7 times and preferably 3.0 to 6 times. Next, the thus stretched sheet is stretched in the direction perpendicular to the stretching direction of the first stage. In this case, the stretching temperature is usually 70 to 170° C., and the stretch ratio is usually 3.0 to 7 times and preferably 3.5 to 6 times. Successively, the resulting biaxially stretched sheet is heat-treated at a temperature of 180 to 270° C. under a tension or relaxation within 30% to obtain a biaxially stretched film. Upon the above stretching steps, there may also be used the method in which the stretching in each direction is carried out in two or more stages. In such a case, the multi-stage stretching is preferably performed such that the stretch ratio in each of the two directions is finally fallen within the above-specified range.
Also, upon producing the polyester film constituting the laminated polyester film according to the present invention, there may also be used a simultaneous biaxial stretching method. The simultaneous biaxial stretching method is such a method in which the above unstretched sheet is stretched and oriented in both of the machine and width directions at the same time while maintaining the sheet in a suitable temperature-controlled condition at a temperature of usually 70 to 120° C. and preferably 80 to 110° C. The stretch ratio used in the simultaneous biaxial stretching method is 4 to 50 times, preferably 7 to 35 times and more preferably 10 to 25 times in terms of an area ratio of the film. Successively, the obtained biaxially stretched sheet is heat-treated at a temperature of 170 to 250° C. under a tension or relaxation within 30% to obtain a stretched oriented film. As the apparatus used in the above simultaneous biaxial stretching method, there may be employed those stretching apparatuses of any conventionally known type such as a screw type stretching apparatus, a pantograph type stretching apparatus and a linear drive type stretching apparatus.
Next, the method of forming the coating layer constituting the laminated polyester film according to the present invention is explained. The coating layer may be formed by either an in-line coating method in which the surface of the polyester film is subjected to coating treatment during the stretching step of the polyester film or an off-line coating method in which the polyester film once produced is transferred to an outside of the film production system and subjected to coating treatment, or by combination of these methods. Among these methods, the in-line coating method is preferably used because the coating layer can be produced simultaneously with formation of the polyester film and therefore obtained at low costs, and the thicknesses of the coating layer can be adjusted by controlling a stretch ratio of the polyester film.
For example, in a sequential biaxial stretching method, the in-line coating treatment may be carried out, in particular, after completion of the longitudinal stretching but before initiation of the lateral stretching, although not particularly limited thereto. When the coating layer is formed on the polyester film by the in-line coating method, the coating can be carried out simultaneously with formation of the polyester film, and the coating layer can be treated at a high temperature. As a result, it is possible to produce a film suitable as the polyester film used in the present invention.
In the present invention, it is essentially required that the polyester film is provided, on at least one surface thereof, with the coating layer which is formed by applying a coating solution comprising an acrylic resin, an epoxy compound and an oxazoline compound thereonto.
The coating layer formed according to the present invention is capable of enhancing an adhesion property to not only a light diffusion layer, an anti-sticking layer or the like, but also various heat-curing layers and active energy ray-curing layers.
As a result of various studies, the present inventors have found that when using an acrylic resin in combination with one kind of crosslinking agent such as an epoxy compound or an oxazoline compound to form a coating layer, the resulting coating layer can be enhanced in adhesion to the light diffusion layer, the anti-sticking layer, etc. As a result of further continuous studies, the present inventors have found that a coating layer formed by using an acrylic resin in combination with both an epoxy compound and an oxazoline compound exhibits a very excellent adhesion property to these layers.
The acrylic resin used in the present invention is a polymer obtained from a polymerizable monomer having a carbon-to-carbon double bond such as, typically, an acrylic monomer and a methacrylic monomer. The polymer may be in the form of either a homopolymer or a copolymer. The polymer may also include a copolymer of the polymer and the other polymer (for example, a polyester, a polyurethane, etc.). Examples of the copolymer include a block copolymer and a graft copolymer. In addition, the polymer may also include a polymer obtained by polymerizing the polymerizable monomer having a carbon-to-carbon double bond in a polyester solution or a polyester dispersion (which may also be in the form of a mixture of the polymers). Further, the polymer may also include a polymer obtained by polymerizing the polymerizable monomer having a carbon-to-carbon double bond in a polyurethane solution or a polyurethane dispersion (which may also be in the form of a mixture of the polymers). Similarly, the polymer may also include a polymer obtained by polymerizing the polymerizable monomer having a carbon-to-carbon double bond in the other polymer solution or the other polymer dispersion (which may also be in the form of a mixture of the polymers).
The above polymerizable monomer having a carbon-to-carbon double bond is not particularly limited. Examples of the typical compounds as the polymerizable monomer include various carboxyl group-containing monomers such as acrylic acid, methacrylic acid, crotonic acid, itaconic acid, fumaric acid, maleic acid and citraconic acid, and salts thereof; various hydroxyl group-containing monomers such as 2-hydroxyethyl (meth)acrylate, 2-hydroxypropyl (meth)acrylate, 4-hydroxybutyl (meth)acrylate, monobutylhydroxyl fumarate and monobutylhydroxyl itaconate; various (meth)acrylic acid esters such as methyl (meth)acrylate, ethyl (meth)acrylate, propyl (meth)acrylate, butyl (meth)acrylate and lauryl (meth)acrylate; various nitrogen-containing vinyl-based monomers such as (meth)acrylamide, diacetone acrylamide, N-methylol acrylamide and (meth)acrylonitrile; various styrene derivatives such as styrene, α-methyl styrene, divinyl benzene and vinyl toluene; various vinyl esters such as vinyl acetate and vinyl propionate; various silicon-containing polymerizable monomers such as γ-methacryloxypropyl trimethoxysilane and vinyl trimethoxysilane; various phosphorus-containing vinyl-based monomers; various halogenated vinyl-based monomers such as vinyl chloride, vinylidene chloride, vinyl fluoride, vinylidene fluoride, trifluorochloroethylene, tetrafluoroethylene, chlorotrifluoroethylene and hexafluoropropylene; and various conjugated dienes such as butadiene.
In order to enhance adhesion of the coating layer to the light diffusion layer, the anti-sticking layer and the like, there are preferably used acrylic resins having a functional group such as a hydroxyl group, an amino group and an amide group.
Upon forming the coating layer of the film according to the present invention, for the purposes of increasing a coating film strength of the obtained coating layer, allowing the coating layer to exhibit a sufficient adhesion property to various layers such as a light diffusion layer and an anti-sticking layer, and enhancing a wet heat resistance, etc., of the film after forming these layers on the coating layer, the coating layer comprises an epoxy compound and an oxazoline compound as a crosslinking agent.
As the epoxy compound, there may be used compounds having an epoxy group in a molecule thereof, and prepolymers and cured products of the compounds. Examples of the epoxy compound include condensates of epichlorohydrin with a hydroxyl group of ethylene glycol, polyethylene glycol, glycerol, polyglycerol, bisphenol A, etc., or an amino group. Specific examples of the epoxy compound include polyepoxy compounds, diepoxy compounds, monoepoxy compounds and glycidyl amine compounds. Examples of the polyepoxy compounds include sorbitol polyglycidyl ether, polyglycerol polyglycidyl ether, pentaerythritol polyglycidyl ether, diglycerol polyglycidyl ether, triglycidyl tris(2-hydroxyethyl)isocyanate, glycerol polyglycidyl ether and trimethylolpropane polyglycidyl ether. Examples of the diepoxy compounds include neopentyl glycol diglycidyl ether, 1,6-hexanediol diglycidyl ether, resorcin diglycidyl ether, ethylene glycol diglycidyl ether, polyethylene glycol diglycidyl ether, propylene glycol diglycidyl ether, polypropylene glycol diglycidyl ether and polytetramethylene glycol diglycidyl ether. Examples of the monoepoxy compounds include allyl glycidyl ether, 2-ethylhexyl glycidyl ether and phenyl glycidyl ether. Examples of the glycidyl amine compounds include N,N,N′,N′-tetraglycidyl-m-xylylenediamine and 1,3-bis(N,N-diglycidylamino)cyclohexane.
In particular, among these epoxy compounds, preferred are polyfunctional epoxy compounds, and more preferred are polyfunctional epoxy compounds having at least two glycidyl ether structures. Examples of the commercially available products of the epoxy compounds include “DECONAL EX-521” (as polyglycerol polyglycidyl ether) produced by Nagase Chemtex Co., Ltd., etc.
Examples of the oxazoline compound include those compounds having an oxazoline group in a molecule thereof. Especially preferred are polymers having an oxazoline group which may be in the form of a homopolymer of an addition-polymerizable oxazoline group-containing monomer or a copolymer of the addition-polymerizable oxazoline group-containing monomer with the other monomer. Examples of the addition-polymerizable oxazoline group-containing monomer include 2-vinyl-2-oxazoline, 2-vinyl-4-methyl-2-oxazoline, 2-vinyl-5-methyl-2-oxazoline, 2-isopropenyl-2-oxazoline, 2-isopropenyl-4-methyl-2-oxazoline and 2-isopropenyl-5-ethyl-2-oxazoline. These oxazoline compounds may be used alone or in the form of a mixture of any two or more thereof. Among these oxazoline compounds, 2-isopropenyl-2-oxazoline is more preferred because of industrial availability thereof. The other monomers used in the copolymer are not particularly limited as long as they are copolymerizable with the addition-polymerizable oxazoline group-containing monomer. Examples of the other monomers include (meth)acrylic acid esters such as alkyl (meth)acrylates (in which the alkyl group may be methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, t-butyl, 2-ethylhexyl or cyclohexyl); unsaturated carboxylic acids such as acrylic acid, methacrylic acid, itaconic acid, maleic acid, fumaric acid, crotonic acid, styrenesulfonic acid and salts of these acids (such as sodium salts, potassium salts, ammonium salts and tertiary amine salts); unsaturated nitriles such as acrylonitrile and methacrylonitrile; unsaturated amides such as (meth)acrylamide, N-alkyl (meth)acrylamide and N,N-dialkyl (meth)acrylamide (in which the alkyl group may be methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, t-butyl, 2-ethylhexyl or cyclohexyl); vinyl esters such as vinyl acetate and vinyl propionate; vinyl ethers such as methyl vinyl ether and ethyl vinyl ether; α-olefins such as ethylene and propylene; halogen-containing α,β-unsaturated monomers such as vinyl chloride, vinylidene chloride and vinyl fluoride; and α,β-unsaturated aromatic monomers such as styrene and α-methyl styrene. These other monomers may be used alone or in combination of any two or more thereof.
In particular, among these oxazoline compounds, preferred are those polymers having an oxazoline group on a side chain thereof. Such polymers may be readily obtained by polymerizing the addition-polymerizable oxazoline group-containing monomer with the other monomer. Examples of the commercial product of the oxazoline compound produced using an acrylic monomer as the other monomer include “EPOCROSS WS-500” and “EPOCROSS WS-300” (both produced by Nippon Shokubai Co., Ltd.) which are in the form of a polymer-type crosslinking agent in which an oxazoline group is bonded as a branched chain to an acrylic resin.
As described above, it has been found that a coating layer formed by using an acrylic resin in combination with both an epoxy compound and an oxazoline compound exhibits a very excellent adhesion property. However, it has also been found that when subjected to much severer durability test, the coating layer still tends to be deteriorated in adhesion property. As a result, it has been found that when further using a melamine compound in combination with the above components in the coating layer, the thus obtained coating layer can exhibit a highly stable adhesion property even after subjected to the durability test.
The melamine compounds used in the present invention are compounds having a melamine skeleton therein. Examples of the melamine compounds include alkylolated melamine derivatives, partially or completely etherified compounds obtained by reacting the alkylolated melamine derivative with an alcohol, and a mixture of these compounds. Examples of the alcohol suitably used for the above etherification include methyl alcohol, ethyl alcohol, isopropyl alcohol, n-butanol and isobutanol. The melamine compound may be either a monomer or a dimer or higher polymer, or may be in the form of a mixture thereof. In addition, there may also be used those compounds obtained by co-condensing a urea or the like to a part of melamine. Further, a catalyst may also be used to enhance a reactivity of the melamine compound. In particular, among these melamine compounds, preferred are alkylated melamine compounds, and more preferred are completely alkylated melamine compounds. Specific examples of the completely alkylated melamine compounds include hexamethoxymethyl melamine and the like.
In the laminated polyester film according to the present invention, in order to improve surface properties of the coating layer and enhance a visibility when forming various layers such as a light diffusion layer and an anti-sticking layer on the surface of the coating layer as well as improve a transparency of the resulting film, a binder polymer other than the above acrylic resin may be used in combination therewith.
The “binder polymer” used in the present invention is defined as a high-molecular compound having a number-average molecular weight (Mn) of not less than 1000 as measured by gel permeation chromatography (GPC) according to a flow scheme for evaluation of safety of high-molecular compounds (Council of Chemical Substances; November, 1985), and exhibiting a good film-forming property.
Specific examples of the binder polymer include polyester resins, urethane resins, polyvinyl resins (such as polyvinyl alcohol, polyvinyl chloride and vinyl chloride-vinyl acetate copolymers), polyalkylene glycols, polyalkylene imines, methyl cellulose, hydroxy cellulose, starches, etc. Among the above binder polymers, in particular, from the viewpoints of enhancing surface properties of the coating layer and an adhesion property, the polyester resins are preferably used in combination with the other binder polymers.
Also, in particular, when forming a light diffusion layer or an anti-sticking layer having a high transparency on the coating layer, there tend to occur remarkable interference fringes. In order to reduce occurrence of the interference fringes when forming the light diffusion layer or the anti-sticking layer having a high transparency on the coating layer, it is possible to control a refractive index of the coating layer. In general, the interference fringes may be often caused owing to a low refractive index of the coating layer. Therefore, occurrence of the interference fringes may be reduced by using a high-refractive index material in combination with the above binder polymers, etc., in the coating layer. As the high-refractive index material, there may be used conventionally known materials. In view of a capability of preventing deterioration of the adhesion property, there may be used, for example, the method of incorporating a condensed polycyclic aromatic compound in the above binder polymers. Among the binder polymers, in particular, the polyester resin is capable of incorporating a larger number of condensed polycyclic aromatic groups therein, and therefore can be more effectively used for controlling a refractive index of the coating layer.
As the method of incorporating the condensed polycyclic aromatic structure into the polyester resins, there may be used the method of introducing two or more hydroxyl groups as substituent groups into the condensed polycyclic aromatic compound to provide a diol component or a polyhydric hydroxyl group component, or the method of introducing two or more carboxyl groups as substituent groups into the condensed polycyclic aromatic compound to provide a dicarboxylic acid component or a polycarboxylic acid component.
From the standpoint of less coloration of the film upon the production process of the laminated polyester film, the condensed polycyclic aromatic compound to be incorporated in the coating layer is preferably a compound having a naphthalene skeleton. In addition, from the viewpoints of good adhesion to a light diffusion layer, an anti-sticking layer or the like to be formed on the coating layer or a good transparency of the resulting film, there can be suitably used resins into which the naphthalene skeleton is incorporated as a constituting component of the polyester. Typical examples of the naphthalene skeleton include 1,5-naphthalenedicarboxylic acid, 2,6-naphthalenedicarboxylic acid and 2,7-naphthalenedicarboxylic acid.
Also, in order to improve a slipping property of the coating layer and an anti-blocking property of the resulting film, the coating layer may also comprise particles. Examples of the particles which may be used in the coating layer include inorganic particles such as particles of silica, alumina, metal oxides and the like, and organic particles such as crosslinked polymer particles.
Further, the coating layer may also comprise various additives such as a defoaming agent, a coatability improver, a thickening agent, an organic lubricant, an antistatic agent, an ultraviolet absorber, an antioxidant, a foaming agent and a dye, if required, unless the subject matter of the present invention is adversely affected thereby.
In the present invention, the content of the above acrylic resin in the coating layer is usually 20 to 90% by weight, preferably 25 to 85% by weight and more preferably 30 to 80% by weight. When the content of the acrylic resin in the coating layer is less than 20% by weight, the resulting coating layer tends to be insufficient in adhesion property owing to the less content of the acrylic resin component. When the content of the acrylic resin in the coating layer is more than 90% by weight, the resulting coating layer tends to become brittle owing to the less content of the crosslinking agent component, and therefore tends to be insufficient in adhesion property or wet heat resistance.
In the present invention, the total content of the epoxy compound and the oxazoline compound in the coating layer is usually 10 to 80% by weight, preferably 15 to 75% by weight and more preferably 20 to 70% by weight. When the total content of the epoxy compound and the oxazoline compound in the coating layer is less than 10% by weight, the resulting coating layer tends to become brittle and therefore tends to be incapable of fully withstanding moisture and heat applied thereto. When the total content of the epoxy compound and the oxazoline compound in the coating layer is more than 80% by weight, the resulting coating layer tends to be insufficient in adhesion property. In addition, the content of at least one of the epoxy compound and the oxazoline compound is preferably more than 5% by weight. When the contents of both the epoxy compound and the oxazoline compound are not more than 5% by weight, the resulting coating layer tends to be unstable in adhesion to the light diffusion layer, the anti-sticking layer, etc., when exposed to high-temperature and high-humidity conditions for a long period of time. In addition, the weight ratio between the epoxy compound and the oxazoline compound in the coating layer is usually 1 to 10:1 to 10, and preferably 1 to 3:1 to 3.
In the present invention, the content of the melamine compound in the coating layer is usually 1 to 50% by weight, preferably 5 to 30% by weight and more preferably 8 to 20% by weight based on a total amount of the acrylic resin, the epoxy compound and the oxazoline compound in the coating layer. When the content of the melamine compound in the coating layer is less than 1% by weight, the resulting coating layer may fail to sufficiently exhibit an effect of stabilizing an adhesion property of the coating layer even after subjected to the durability test. When the content of the melamine compound in the coating layer is more than 50% by weight, the coating layer tends to be insufficient in adhesion property owing to a less content of the other components.
The polyester film used in the present invention may also be provided, on its surface opposed to the surface on which the above coating layer is formed, with an additional coating layer. For examples, in the case where a functional layer such as an anti-sticking layer, a prism layer, a micro-lens layer and a hard coat layer is to be formed on the surface of the polyester film which is opposed to the surface on which the light diffusion layer is formed, the coating layer formed on the opposite surface of the polyester film is capable of enhancing an adhesion property to such a functional layer. The coating layer formed on the opposite surface of the polyester film may comprise conventionally known components, for example, a binder polymer such as polyester resins, acrylic resins and urethane resins, a crosslinking agent such as an epoxy compound, an oxazoline compound, a melamine compound and an isocyanate compound, etc. These components or materials may be respectively used alone or in combination of any two or more thereof. In addition, the coating layer formed on the opposite surface of the polyester film may be the same as the above coating layer formed from the acrylic resin, the epoxy compound and the oxazoline compound (i.e., the same coating layer may be formed on both side surfaces of the polyester film). In view of facilitated production and film processing, the coating layers formed on the opposite surfaces of the polyester film are preferably identical to each other.
The analysis of the components contained in the coating layer may be conducted, for example, by surface analysis such as TOF-SIMS.
When forming the coating layer by in-line coating, the laminated polyester film is preferably produced by the method in which an aqueous solution or a water dispersion comprising a series of the above mentioned compounds is prepared as a coating solution having a concentration of about 0.1 to about 50% by weight in terms of a solid content thereof, and the thus prepared coating solution is applied onto the polyester film. The coating solution may also comprise a small amount of an organic solvent for the purpose of improving a dispersibility in water, a film-forming property, etc., unless the subject matter of the present invention is adversely affected thereby. The organic solvents may be used alone, or may be appropriately used in the form of a mixture of any two or more thereof.
In the laminated polyester film of the present invention, the film thickness of the coating layer formed on the polyester film is usually in the range of 0.002 to 1.0 g/m2, preferably 0.01 to 0.5 g/m2 and more preferably 0.02 to 0.2 g/m2. When the film thickness of the coating layer is less than 0.002 g/m2, the resulting coating layer may fail to exhibit a sufficient adhesion property. When the film thickness of the coating layer is more than 1.0 g/m2, the resulting coating layer tends to be deteriorated in appearance and transparency, and the obtained laminated film tends to be deteriorated in anti-blocking property.
In the present invention, as the method of forming the coating layer, there may be used conventionally known coating methods such as a reverse gravure coating method, a direct gravure coating method, a roll coating method, a die coating method, a bar coating method and a curtain coating method.
In the present invention, the drying and curing conditions used upon forming the coating layer on the polyester film are not particularly limited. For example, in the case where the coating layer is formed in an off-line coating manner, the coating layer may be subjected to heat treatment usually at a temperature of 80 to 200° C. for 3 to 40 sec and preferably at a temperature of 100 to 180° C. for 3 to 40 sec.
On the other hand, in the case where the coating layer is formed in an in-line coating manner, the coating layer may be subjected to heat treatment usually at a temperature of 70 to 280° C. for 3 to 200 sec.
In any of the off-line coating and in-line coating methods, the heat treatment may be used in combination with irradiation with active energy rays such as irradiation with ultraviolet rays, if required. The polyester film constituting the laminated polyester film of the present invention may be previously subjected to surface treatments such as corona treatment and plasma treatment.
In the laminated polyester film of the present invention, a light diffusion layer, an anti-sticking layer, etc., may be formed on the coating layer. The light diffusion layer may comprise particles and a binder.
As the particles incorporated in the light diffusion layer, there may be used those particles having properties capable of diffusing light therein. Examples of the particles include organic particles of acrylic resins, acrylic urethane resins, urethane resins, polyester resins, polyvinyl resins, etc., and inorganic particles of silica, metal oxides, barium sulfate, etc. Among these particles, acrylic resins and acrylic urethane resins are preferably used because of a good transparency thereof. The particle diameter of these particles is not particularly limited, and an average particle diameter thereof is preferably 1 to 50 μm and more preferably 5 to 15 μm.
The binder incorporated in the light diffusion layer is used for fixing the particles therein and allowing the light diffusion layer to exhibit a light diffusion property. Examples of the binder include polyester resins, acrylic resins, polyurethane resins, fluororesins, silicone-based resins, epoxy resins and ultraviolet-curable resins. Also, in view of a good processability, polyol compounds can be suitably used as the binder. Examples of the polyol compounds include acrylic polyols and polyester polyols.
When the polyol compound is used as the binder, an isocyanate is suitably used as a curing agent. When incorporating the isocyanate into the binder, it is possible to form a strong crosslinked structure, resulting in improved properties of the light diffusion layer. In addition, when the ultraviolet-curable resin is used as the binder, the resin is preferably an acrylic resin, so that the resulting light diffusion layer can be enhanced in hardness thereof.
The light diffusion layer may also comprise various additives such as a surfactant, a microfine inorganic filler, a plasticizer, a curing agent, an antioxidant, an ultraviolet absorber and a rust preventive agent unless a light diffusion performance of the light diffusion layer is adversely affected thereby.
The mixing ratio between the binder and the particles in the light diffusion layer may be appropriately determined according to the aimed light diffusion property of the light diffusion layer. For example, the weight ratio of the binder to the particles [binder/particles] is in the range of 0.1 to 50 and preferably 0.5 to 20 although not particularly limited thereto.
As the method of forming the light diffusion layer, there may be used the method in which a coating solution comprising the binder and the particles is prepared and then applied and dried. Examples of the coating method used for forming the light diffusion layer include conventionally known coating methods such as a reverse gravure coating method, a direct gravure coating method, a roll coating method, a die coating method, a bar coating method, a curtain coating method, a spray coating method and a spin coating method. The thickness of the light diffusion layer is not particularly limited, and is in the range of 1 to 100 μm and preferably 3 to 30 μm in view of a good light diffusion property and a high film strength of the resulting layer, etc.
On the surface of the polyester film which is opposite to the surface where the light diffusion layer is provided, the anti-sticking layer may be formed thereon. The anti-sticking layer may comprise a binder and particles similarly to those used in the light diffusion layer. The particles to be incorporated in the anti-sticking layer may generally have a smaller particle diameter and a less content as compared to those in the light diffusion layer because the anti-sticking layer is not required to exhibit a light diffusion property by the particles. The anti-sticking layer may be formed by the same method as used for production of the light diffusion layer. The thickness of the anti-sticking layer is not particularly limited, and is preferably in the range of 1 to 10 μm.
The present invention is described in more detail below by Examples. However, these Examples are only illustrative and not intended to limit the present invention thereto. In addition, the measuring and evaluating methods used in the present invention are as follows.
One gram of a polyester from which the other polymer components incompatible with the polyester and pigments were previously removed was accurately weighed, and mixed with and dissolved in 100 mL of a mixed solvent comprising phenol and tetrachloroethane at a weight ratio of 50:50, and a viscosity of the resulting solution was measured at 30° C.
(2) Measurement of Average Particle Diameter (d50: μm):
Using a centrifugal precipitation type particle size distribution measuring apparatus “SA-CP3 Model” manufactured by Shimadzu Seisakusho Co., Ltd., the value of a particle size corresponding to a cumulative fraction of 50% (based on the weight) in equivalent spherical distribution of the particles was measured to determine an average particle diameter thereof.
A coating solution for a light diffusion layer comprising 100 parts by mass of a resin (“HALS-HYBRID UV-G301” produced by Nippon Shokubai Co., Ltd.), 10 parts by mass of an isocyanate (“DESMODUR N-3200” produced by SUMIKA BAYER URETHANE Co., Ltd.), 30 parts by mass of acrylic resin particles having an average particle diameter of 15 μm (“MBX-15” produced by Sekisui Plastics Co., Ltd.), 100 parts by mass of toluene and 100 parts by mass of methyl ethyl ketone was prepared, applied on a surface of a polyester film through a coating layer, and then heated and cured to thereby form a light diffusion layer having a thickness of 15 g/m2. In addition, a coating solution for an anti-sticking layer was prepared by the same method as used for production of the coating solution for a light diffusion layer except for using 7 parts by mass of acrylic resin particles having an average particle diameter of 5 μm (“MBX-5” produced by Sekisui Plastics Co., Ltd.) in place of the acrylic resin particles having an average particle diameter of 15 μm. The thus prepared coating solution for an anti-sticking layer was applied on the surface of the polyester film opposed to the surface on which the above light diffusion layer was formed, and then heated and cured to form an anti-sticking layer having a thickness of 3 g/m2, thereby obtaining a both side-coated polyester film. Thereafter, the thus obtained light diffusion layer and anti-sticking layer were respectively subjected to cross-cutting to form 100 (10×10) cross-cuts thereon. A 18 mm-wide tape (“Cellotape (registered trademark) CT-18” produced by Nichiban Co., Ltd.) was attached onto each of the light diffusion layer and anti-sticking layer, and then rapidly peeled off therefrom at a peel angle of 180°. Then, the surface of each of the light diffusion layer and anti-sticking layer from which the tape was peeled off was observed and the surfaces of light diffusion layer and anti-sticking layer were compared. The surface where the larger area was peeled off was selected and the selected surface was rated as follows.
A: Peeled area of each of the light diffusion layer and the anti-sticking layer was not more than 5% based on the larger peeled-off area thereof.
B: Peeled area of each of the light diffusion layer and the anti-sticking layer was more than 5% and not more than 30% based on the larger peeled-off area thereof.
C: Peeled area of each of the light diffusion layer and the anti-sticking layer was more than 30% based on the larger peeled-off area thereof.
The anti-sticking layer having a less amount of surface irregularities usually exhibits a higher adhesion property to the tape to be peeled off therefrom, and therefore the peeled area of the anti-sticking layer tends to be larger than that of the light diffusion layer.
A coating solution for a light diffusion layer comprising 60 parts by mass of dipentaerythritol hexaacrylate, 6 parts by mass of 2-hydroxy-3-phenoxypropyl acrylate, 4 parts by mass of a photopolymerization initiator (“IRGACURE 184” produced by Ciba Specialty Chemicals Corp.), 30 parts by mass of acrylic resin particles having an average particle diameter of 12 μm (“MBX-12” produced by Sekisui Plastics Co., Ltd.) and 200 parts by mass of methyl ethyl ketone was prepared, applied on a surface of a polyester film through a coating layer, and cured by irradiation with ultraviolet rays to form a light diffusion layer having a thickness of 10 g/m2. In addition, a coating solution for an anti-sticking layer was prepared by the same method as used for production of the above coating solution for a light diffusion layer except for using 5 parts by mass of acrylic resin particles having an average particle diameter of 5 μm (“MBX-5” produced by Sekisui Plastics Co., Ltd.) in place of the acrylic resin particles having an average particle diameter of 12 μm. The thus prepared coating solution for an anti-sticking layer was applied on the surface of the polyester film opposed to the surface on which the above light diffusion layer was formed, and then cured by irradiation with ultraviolet rays to form an anti-sticking layer having a thickness of 3 g/m, thereby obtaining a both side-coated polyester film. Immediately after forming the layers (initial) and after allowing the film to stand under the environmental conditions of 80° C. and 90% RH for 150 hr (wet heat test), the light diffusion layer and anti-sticking layer were respectively subjected to cross-cutting to form 100 (10×10) cross-cuts thereon. A 18 mm-wide tape (“Cellotape (registered trademark) CT-18” produced by Nichiban Co., Ltd.) was attached onto each of the light diffusion layer and anti-sticking layer, and then rapidly peeled off therefrom at a peel angle of 180°. Then, the surface of each of the light diffusion layer and anti-sticking layer from which the tape was peeled off was observed and the surfaces of light diffusion layer and anti-sticking layer were compared. The surface where the larger area was peeled off was selected and the selected surface was rated as follows.
A: Peeled area of each of the light diffusion layer and the anti-sticking layer was not more than 5% based on the larger peeled-off area thereof.
B: Peeled area of each of the light diffusion layer and the anti-sticking layer was more than 5% and not more than 30% based on the larger peeled-off area thereof.
C: Peeled area of each of the light diffusion layer and the anti-sticking layer was more than 30% based on the larger peeled-off area thereof.
The anti-sticking layer having a less amount of surface irregularities usually exhibits a higher adhesion property to the tape to be peeled off therefrom, and therefore the peeled area of the anti-sticking layer tends to be larger than that of the light diffusion layer.
A coating solution for a light diffusion layer comprising 90 parts by mass of dipentaerythritol hexaacrylate, 10 parts by mass of 2-hydroxy-3-phenoxypropyl acrylate, 5 parts by mass of a photopolymerization initiator (“IRGACURE 184” produced by Ciba Specialty Chemicals Corp.), 30 parts by mass of acrylic resin particles having an average particle diameter of 15 μm (“MBX-15” produced by Sekisui Plastics Co., Ltd.), 100 parts by mass of toluene and 100 parts by mass of methyl ethyl ketone was prepared, applied on a surface of a polyester film through a coating layer, and cured by irradiation with ultraviolet rays to form a light diffusion layer having a thickness of 10 g/m2. In addition, a coating solution for an anti-sticking layer was prepared by the same method as used for production of the above coating solution for a light diffusion layer except for using 7 parts by mass of acrylic resin particles having an average particle diameter of 5 μm (“MBX-5” produced by Sekisui Plastics Co., Ltd.) in place of the acrylic resin particles having an average particle diameter of 15 μm. The thus prepared coating solution for an anti-sticking layer was applied on the surface of the polyester film opposed to the surface on which the above light diffusion layer was formed, and then cured by irradiation with ultraviolet rays to form an anti-sticking layer having a thickness of 3 g/m2, thereby obtaining a both side-coated polyester film. Immediately after forming the layers (initial) and after allowing the film to stand under the environmental conditions of 80° C. and 90% RH for 150 hr (wet heat test) and further after immersing the film in boiled hot water for 20 min (hot water test), the light diffusion layer and anti-sticking layer were respectively subjected to cross-cutting to form 100 (10×10) cross-cuts thereon. A 18 mm-wide tape (“Cellotape (registered trademark) CT-18” produced by Nichiban Co., Ltd.) was attached onto each of the light diffusion layer and anti-sticking layer, and then rapidly peeled off therefrom at a peel angle of 180°. Then, the surface of each of the light diffusion layer and anti-sticking layer from which the tape was peeled off was observed and the surfaces of light diffusion layer and anti-sticking layer were compared. The surface where the larger area was peeled off was selected and the selected surface was rated as follows.
A: Peeled area of each of the light diffusion layer and the anti-sticking layer was not more than 5% based on the larger peeled-off area thereof.
B: Peeled area of each of the light diffusion layer and the anti-sticking layer was more than 5% and not more than 30% based on the larger peeled-off area thereof.
C: Peeled area of each of the light diffusion layer and the anti-sticking layer was more than 30% based on the larger peeled-off area thereof.
The anti-sticking layer having a less amount of surface irregularities usually exhibits a higher adhesion property to the tape to be peeled off therefrom, and therefore the peeled area of the anti-sticking layer tends to be larger than that of the light diffusion layer.
The polyesters used in the respective Examples and Comparative Examples were prepared as follows.
One hundred parts by weight of dimethyl terephthalate and 60 parts by weight of ethylene glycol as starting materials were charged together with tetrabutoxytitanate as a catalyst into a reaction vessel, and the reaction therebetween was initiated at 150° C. The reaction temperature was gradually raised while distilling off methanol as produced, and allowed to reach 230° C. after 3 hr. After 4 hr, the transesterification reaction was substantially terminated, and then the resulting product was subjected to polycondensation reaction for 4 hr. More specifically, the reaction temperature was gradually raised from 230° C. until reaching 280° C. On the other hand, the reaction pressure was gradually reduced from normal pressure until finally reaching 0.3 mmHg. After initiation of the reaction, the change in agitation power in the reaction vessel was monitored, and the reaction was terminated at the time at which a viscosity of the reaction solution reached the value corresponding to an intrinsic viscosity of 0.63 on the basis of the change in agitation power in the reaction vessel. The resulting polymer was discharged under application of a nitrogen pressure from the reaction vessel, thereby obtaining a polyester (A) having an intrinsic viscosity of 0.63.
One hundred parts by weight of dimethyl terephthalate and 60 parts by weight of ethylene glycol as starting materials were charged together with magnesium acetate tetrahydrate as a catalyst into a reaction vessel, and the reaction therebetween was initiated at 150° C. The reaction temperature was gradually raised while distilling off methanol as produced, and allowed to reach 230° C. after 3 hr. After 4 hr, the transesterification reaction was substantially terminated. The obtained reaction mixture was transferred to a polycondensation reaction vessel, and mixed with orthophosphoric acid and then with germanium dioxide, followed by subjecting the resulting mixture to polycondensation reaction for 4 hr. More specifically, the reaction temperature was gradually raised from 230° C. until reaching 280° C. On the other hand, the reaction pressure was gradually reduced from normal pressure until finally reaching 0.3 mmHg. After initiation of the reaction, the change in agitation power in the reaction vessel was monitored, and the reaction was terminated at the time at which a viscosity of the reaction solution reached the value corresponding to an intrinsic viscosity of 0.65 on the basis of the change in agitation power in the reaction vessel. The resulting polymer was discharged under application of a nitrogen pressure from the reaction vessel, thereby obtaining a polyester (B) having an intrinsic viscosity of 0.65.
The same procedure as defined in the above method for producing the polyester (A) was conducted except that silica particles having an average particle diameter of 2.0 μm in the form of a dispersion in ethylene glycol were added in an amount of 0.2 part, and the polycondensation reaction was terminated at the time at which a viscosity of the reaction solution reached the value corresponding to an intrinsic viscosity of 0.66, thereby obtaining a polyester (C) having an intrinsic viscosity of 0.66.
The compounds constituting the coating layer are as follows.
Acrylic resin: (IA) Water dispersion of an acrylic resin obtained by polymerizing the following composition:
Emulsion polymer (emulsifier: anionic surfactant) produced from ethyl acrylate/n-butyl acrylate/methyl methacrylate/N-methylol acrylamide/acrylic acid=65/21/10/2/2 (% by weight)
Acrylic resin: (IB) Water dispersion of an acrylic resin obtained by polymerizing the following composition:
Emulsion polymer (emulsifier: anionic surfactant) produced from ethyl acrylate/methyl methacrylate/2-hydroxyethyl methacrylate/N-methylol acrylamide/acrylic acid=65/28/3/2/2 (% by weight)
Polyester resin: (IIA) Water dispersion of a polyester resin obtained by copolymerizing the following composition:
Monomer composition: (acid component) terephthalic acid/isophthalic acid/5-sodium sulfoisophthalic acid//(diol component) ethylene glycol/1,4-butanediol/diethylene glycol=56/40/4//70/20/10 (mol %)
Polyester resin comprising a condensed polycyclic aromatic compound: (IIB) Water dispersion of a polyester resin obtained by copolymerizing the following composition:
Monomer composition: (acid component) 2,6-naphthalenedicarboxylic acid/5-sodium sulfoisophthalic acid//(diol component) ethylene glycol/diethylene glycol=92/8//80/20 (mol %)
Epoxy compound: (III) Polyglycerol polyglycidyl ether “DECONAL EX-521” (produced by Nagase Chemtex Co., Ltd.)
Oxazoline compound: (IVA) Acrylic polymer having an oxazoline group and a polyalkyleneoxide chain; “EPOCROSS WS-500” (produced by Nippon Shokubai Co., Ltd.; compound of a type comprising about 38% by weight of a 1-methoxy-2-propanol solvent)
Oxazoline Compound: (IVB)
Oxazoline group-containing acrylic polymer “EPOCROSS WS-300” (produced by Nippon Shokubai Co., Ltd.)
Melamine compound: (V) Hexamethoxymethyl melamine
Particles: (V) Silica sol having an average particle diameter of 65 nm
A mixed raw material obtained by mixing the polyesters (A), (B) and (C) in amounts of 85%, 5% and 10%, respectively, as a raw material for outermost layers (surface layers), and a mixed raw material obtained by mixing the polyesters (A) and (B) in amounts of 95% and 5%, respectively, as a raw material for an intermediate layer, were respectively charged into two extruders, melted therein at 290° C., and then co-extruded therefrom on a cooling roll whose surface was controlled to a temperature of 40° C. to form a sheet having a two-kind/three-layer structure (discharge amount: surface layer/intermediate layer/surface layer=1:18:1), followed by cooling and solidifying the thus extruded sheet on the cooling roll, thereby obtaining an unstretched sheet. Next, the thus obtained unstretched sheet was stretched utilizing a difference between peripheral speeds of rolls at 85° C. and a stretch ratio of 3.2 times in a longitudinal direction thereof. Thereafter, a coating solution 1 shown in the below-mentioned Table 1 was applied on both surfaces of the thus obtained longitudinally stretched sheet, and then the resulting sheet was introduced into a tenter where the sheet was stretched at 120° C. and a stretch ratio of 3.8 times in a lateral direction thereof and then heat-treated at 225° C. Next, the obtained stretched sheet was relaxed by 2% in a lateral direction thereof, thereby obtaining a polyester film having a thickness of 188 μm which was provided on each surface thereof with a coating layer having a coating amount as shown in Table 2 (after dried).
The thus obtained polyester film was evaluated for various adhesion properties. As a result, it was confirmed that all of the adhesion properties of the polyester film evaluated were good. Various properties of the thus obtained film are shown in Table 2 below.
The same procedure as defined in Example 1 was conducted except that the composition of the coating agent was changed to those as shown in Table 1, thereby obtaining polyester films. Various properties of the thus obtained polyester films are shown in Table 2, i.e., the respective polyester films had good adhesion properties.
The same procedure as defined in Example 1 was conducted except that the composition of the coating agent was changed to those as shown in Table 1, thereby obtaining polyester films. The evaluation results of various properties of the thus obtained laminated polyester films are shown in Table 2, i.e., the polyester films exhibited poor adhesion properties.
The same procedure as defined in Example 1 was conducted except that the composition of the coating agent was changed to those as shown in Table 3, thereby obtaining polyester films. Various properties of the thus obtained polyester films are shown in Table 4, i.e., the respective polyester films had good adhesion properties.
The same procedure as defined in Example 1 was conducted except that the composition of the coating agent was changed to those as shown in Table 3, thereby obtaining polyester films. The evaluation results of various properties of the thus obtained laminated polyester films are shown in Table 4, i.e., the polyester films exhibited poor adhesion properties.
The film of the present invention can be suitably used in the applications requiring a good adhesion property to a light diffusion layer, an anti-sticking layer, etc., for example, in a backlight unit of liquid crystal displays.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2009-156529 | Jul 2009 | JP | national |
| 2009-156533 | Jul 2009 | JP | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/JP2010/061044 | 6/29/2010 | WO | 00 | 2/6/2012 |
