Patent Application
20080069975
1 denotes a transparent support; 2 denotes a hardcoat layer; 3 denotes an organic resin particle; 4 denotes a low refractive index layer; 5 denotes a hardcoat second layer; and 6 denotes a hardcoat first layer.
The present invention is described in detail below. Incidentally, the expression “from (numerical value 1) to (numerical value 2)” as used in the present invention for indicating a physical value, a characteristic value or the like means “(numerical value 1) or more and (numerical value 2) or less”. Also, the term “(meth)acrylate” as used in the present invention means “at least either acrylate or methacrylate”. The same applies to “(meth)acrylic acid” and the like.
The optical film of the present invention has at least one light-transparent resin-containing hardcoat layer on a transparent support. The optical film of the present invention is described by referring to
The optical film of
The hardcoat layer may be formed of a plurality of layers and this is also preferred. The optical film of
The optical film of the present invention is a film in which the percentage change in the entire beam transmittance between before and after the optical film is exposed to an environment at a temperature of 80° C. and a relative humidity of 90% for 500 hours is 5% or less. The “percentage change is 5% or less” means that the percentage change in the entire beam transmittance Ta after exposure under the above-described environmental conditions is 5% or less based on the entire beam transmittance Tb of the film before exposure under the environmental conditions above. The optical film of the present invention is described in detail below.
In view of optical design for obtaining a film having a light-diffusing effect, the refractive index of the hardcoat layer for use in the present invention is preferably from 1.48 to 2.00, more preferably 1.48 to 1.60, still more preferably from 1.48 to 1.55.
In the present invention, the refractive index of the light-transparent organic resin particle described later is higher than the refractive index of the hardcoat layer, and the difference therebetween is preferably from 0.07 to 0.20, more preferably from 0.07 to 0.18, and most preferably from 0.08 to 0.16. If the difference of the refractive index is less than 0.07, a large amount of the particle is required for obtaining the desired internal haze and this gives rise to worsening of the adhesive property and coating suitability on the transparent substrate, whereas if the difference of the refractive index exceeds 0.20, the scattering angle of transmitted light is excessively widened and the front contrast may disadvantageously decrease.
Meanwhile, even when the refractive index of the hardcoat layer is higher than the refractive index of the light-transparent organic resin particle and the difference therebetween is in the above-described range, the effect of the present invention can be obtained. However, in this case, the refractive index of the hardcoat layer must be elevated and a high refractive index fine particle (several nm to tens of nm) such as ZrO2, TiO2 and Al2O3 or high refractive index monomer needs to be incorporated in a large amount into the hardcoat layer, which is not preferred in view of rise in the cost.
Here, the refractive index of the hardcoat layer can be quantitatively evaluated, for example, by directly measuring the refractive index with an Abbe refractometer or by measuring the spectral reflection spectrum or spectral ellipsometry. The refractive index of the light-transparent organic resin particle is determined as follows. The light-transparent particle is dispersed in an equal amount in solvents prepared by changing the mixing ratio of two kinds of solvents differing in the refractive index and thereby varying the refractive index, the turbidity is measured, and the refractive index of the solvent when the turbidity becomes minimum is measured by an Abbe refractometer.
As for the film thickness of the hardcoat layer, from the standpoint of imparting sufficiently high durability and strength to the film as well as in view of curling, the thickness of the hardcoat layer is usually from 3 to 30 μm, preferably from 3 to 20 μm, and most preferably from 5 to 15 μm.
The strength of the hardcoat layer is preferably H or more, more preferably 2H or more, still more preferably 3H or more, in the pencil hardness test.
Furthermore, in the Taber test according to JIS K5400, the abrasion loss of the specimen between before and after the test is preferably smaller.
The binder of the hardcoat layer of the present invention contains either one or both of a heat-curable resin and an ionizing radiation-curable resin and is cured to form the layer.
The heat-curable resin for use in the binder of the hardcoat layer of the present invention includes a fluorine-containing copolymer having a heat-curable functional group, which is described later, and an organosilane compound.
The hardcoat layer of the present invention is preferably formed through a crosslinking or polymerization reaction of an ionizing radiation-curable compound. That is, a coating composition containing an ionizing radiation-curable polyfunctional monomer or polyfunctional oligomer as the binder is coated on a transparent support, and a crosslinking or polymerization reaction of the polyfunctional monomer or polyfunctional oligomer is brought about, whereby the hardcoat layer is formed. The functional group in the ionizing radiation-curable polyfunctional monomer or polyfunctional oligomer is preferably a photo- (ultraviolet ray-), electron beam- or radiation-polymerizable functional group, more preferably a photopolymerizable functional group. Examples of the photopolymerizable functional group include an unsaturated polymerizable functional group such as (meth)acryloyl group, vinyl group, styryl group and allyl group. Among these, a (meth)acryloyl group is preferred.
Specific examples of the photopolymerizable polyfunctional monomer having a photopolymerizable functional group include (meth)acrylic acid diesters of alkylene glycol, such as neopentyl glycol acrylate, 1,6-hexanediol(meth)acrylate and propylene glycol di(meth)acrylate; (meth)acrylic acid diesters of polyoxyalkylene glycol, such as triethylene glycol di(meth)acrylate, dipropylene glycol di(meth)acrylate, polyethylene glycol di(meth)acrylate and polypropylene glycol di(meth)acrylate; (meth)acrylic acid diesters of polyhydric alcohol, such as pentaerythritol di(meth)acrylate; and (meth)acrylic acid diesters of ethylene oxide or propylene oxide adduct, such as 2,2-bis{4-(acryloxy•diethoxy)phenyl}propane and 2-2-bis{4-(acryloxy•polypropoxy)phenyl}propane.
Furthermore, epoxy(meth)acrylates, urethane(meth)acrylates and polyester(meth)acrylates may also be preferably used as the photopolymerizable polyfunctional monomer. Among these, esters of a polyhydric alcohol with a (meth)acrylic acid are preferred, and a polyfunctional monomer having three or more (meth)acryloyl groups within one molecule is more preferred. Specific examples thereof include trimethylolpropane tri(meth)acrylate, trimethylolethane tri(meth)acrylate, 1,2,4-cyclohexane tetra(meth)acrylate, pentaglycerol triacrylate, pentaerythritol tetra(meth)acrylate, pentaerythritol tri(meth)acrylate, (di)pentaerythritol triacrylate, (di)pentaerythritol pentaacrylate, (di)pentaerythritol tetra(meth)acrylate, (di)pentaerythritol hexa(meth)acrylate, tripentaerythritol triacrylate and tripentaerythritol hexatriacrylate. The terms “(meth)acrylate”, “(meth)acrylic acid” and “(meth)acryloyl” as used in the present invention mean “acrylate or methacrylate”, “acrylic acid or methacrylic acid” and “acryloyl or methacryloyl”, respectively.
As for the polyfunctional monomer binder, monomers differing in the refractive index may be used for controlling the refractive index of each layer. In particular, examples of the high refractive index monomer include bis(4-methacryloylthiophenyl)sulfide, vinyl-naphthalene, vinyl phenyl sulfide and 4-methacryloxyphenyl-4′-methoxyphenylthioether. Also, dendrimers described, for example, in JP-A-2005-76005 and JP-A-2005-36105, and norbornene ring-containing monomers described, for example, in JP-A-2005-60425 may be used.
As for the polyfunctional monomer or polyfunctional oligomer binder, two or more kinds of binders may be used in combination. The polymerization of such a binder having an ethylenically unsaturated group may be performed by the irradiation of ionizing radiation or under heating in the presence of a photoradical initiator or a thermal radical initiator.
In the polymerization reaction of the photopolymerizable polyfunctional monomer or polyfunctional oligomer, a photopolymerization initiator is preferably used, and the photopolymerization initiator is preferably a photoradical polymerization initiator or a photocationic polymerization initiator, more preferably a photoradical polymerization initiator.
In the present invention, a polymer or a crosslinked polymer can be used in combination as the binder. The crosslinked polymer preferably has an anionic group. The crosslinked polymer having an anionic group has a structure that the main chain of the polymer having an anionic group is crosslinked.
Examples of the polymer main chain include a polyolefin (saturated hydrocarbon), a polyether, a polyurea, a polyurethane, a polyester, a polyamine, a polyamide and a melamine resin. A polyolefin main chain, a polyether main chain and a polyurea main chain are preferred, a polyolefin main chain and a polyether main chain are more preferred, and a polyolefin main chain is most preferred.
In the binder of the hardcoat layer, for the purpose of controlling the refractive index of the hardcoat layer, a high refractive index monomer, an inorganic particle incapable of producing visible light scattering, that is, an inorganic particle having an average particle size of 100 nm or less, such as ZrO2, TiO2 and SiO2, or both may be added. The inorganic particle has an effect of suppressing the curing shrinkage due to a crosslinking reaction, in addition to the effect of controlling the refractive index. In the present invention, a polymer produced by the polymerization of the above-described polyfunctional monomer and/or high refractive index monomer or the like after the formation of the hardcoat layer is, including the inorganic particle dispersed therein, referred to as a binder.
The haze of the hardcoat layer varies depending on the function imparted to the optical film.
In the case of imparting an antiglare function by the effect of surface scattering of the hardcoat layer, the surface haze is preferably 7% or less, more preferably 5% or less, and most preferably less than 3%.
Also, in the case of imparting a function of making less discernible the liquid crystal panel pattern, color unevenness, brightness unevenness or glaring by the effect of internal scattering of the hardcoat layer or a function of enlarging the viewing angle by the effect of scattering, the internal haze value is preferably from 20 to 95%, more preferably from 35 to 90%, and most preferably from 45 to 85%.
In the film of the present invention, the surface haze and internal haze may be freely set according to the purpose.
As for the surface irregularity shape of the hardcoat layer, out of the properties indicating the surface roughness, for example, the centerline average roughness (Ra) is preferably set to 0.20 μm or less so as to maintain the clearness of image and obtain a clear surface. Ra is more preferably 0.10 μm or less, still more preferably 0.07 μm or less, yet still more preferably less than 0.05 μm. In the film of the present invention, the surface irregularities of the film are mainly governed by the surface irregularities of the hardcoat layer and by adjusting the centerline average roughness of the hardcoat layer, the antireflection film can be made to have a centerline average roughness in the above-described range.
In the hardcoat layer of the present invention, an organic resin particle is used so as to impart antiglare property (surface scattering property) or internal scattering property.
The organic resin particle used in the hardcoat layer of the present invention is a particle having a refractive index of 1.60 or more, such as amino resin particle [e.g., melamine resin particle (refractive index: 1.57 to 1.65), benzoguanamine-melamine formaldehyde particle (refractive index: 1.68)], polystyrene particle (refractive index: 1.60), crosslinked polystyrene particle (refractive index: 1.61), and a polyvinyl chloride particle (refractive index: 1.60).
As regards the amino resin particle for use in the present invention, although not particularly limited, a specific preferred amino resin particle is, for example, a cured resin particle of an amino resin obtained through a reaction using at least one member selected from the amino-based compound group (A) consisting of benzoguanamine, cyclohexane carboguanamine, cyclohexene carboguanamine, melamine, acetoguanamine, norbornene carboguanamine, paratoluene sulfonamide, benzoguananamine(2,4-diamino-6-phenyl-sym.-triazine) and urea (hereinafter sometimes simply referred to as the compound group (A)), and formaldehyde (B), more specifically, a particle of a resin which is obtained by at least partially methylolating the amino group of the compound group (A) with formaldehyde (B) and subjecting the methylolated product to condensation•curing and which has a refractive index of 1.60 to 1.75. The methylolated product indicates generally an initial condensate of the compound group (A) and the formaldehyde (B), preferably a water-compatible initial condensate, and works out to a precursor of the amino resin.
Although not particularly limited, the amino resin particle of the present invention is preferably, for example, white or milky white, more preferably white. By virtue of being white or milky white, like an additive to plastics, the amino resin particle can be preferably used over a wide range of usage, for example, where the substrate is prevented from great change in the color or required to be arbitrarily colored.
Above all, a melamine resin particle and a benzoguanamine-melamine formaldehyde particle are preferred.
Also, a light-transparent organic resin particle in which the particle surface or surface neighborhood is covered with a metal oxide (sometimes referred to as “surface coat”) is preferably used. When the surface or surface neighborhood is covered with a metal oxide, the weather resistance is enhanced and good dispersibility in an organic solvent is obtained. Specific examples of the metal oxide include ZrO2, SiO2, Al2O3, In2O3, ZnO, SnO2 and Sb2O3. Among these, SiO2 is inexpensive and is preferred. As for the surface coat SiO2, a colloidal silica having an average particle diameter of 5 to 70 nm may be coated by the method described in JP-A-2002-327036 or JP-A-2005-171033. The thickness of the metal oxide coat layer on the particle surface or surface neighborhood is preferably 400 nm or less.
When the particle surface after surface coating with a metal oxide is further coated with a hydrophobic organic compound, the water resistance of the particle can be enhanced and weather resistance is further enhanced. In order to bring out the waterproofing effect, an organic compound having a carbon number of 3 or more is preferred. As the number of carbons is larger and the content of the hydrophobic moiety such as aromatic ring is larger, the waterproofing effect becomes higher.
As for the organic compound having a carbon number of 3 or more, a reaction adduct of a long-chain alcohol such as n-hexyl, n-octyl and 2-ethylhexyl, a carboxylic acid or the like is suitably used.
On the particle surface after surface coating with a metal oxide, an organic compound having a reactive group responsive to heat and/or ionizing radiation is preferably further coated and cured.
The organic compound having a reactive group responsive to heat and/or ionizing radiation includes a reaction adduct of an organic compound having a cyclic ether group such as acryloyl group, methacryloyl group, acrylamide group, vinyl ether group and epoxy group, and having a hydroxyl group, a carboxylic acid group or the like through a linking group. Specific preferred examples thereof include a reaction adduct such as trimethylolpropane diacrylate, pentaerythritol triacrylate and dipentaerythritol hexaacrylate.
A reactive group such as ethylenically unsaturated group is contained in the molecule of the organic compound, and an organic compound having on the surface thereof a crosslinked structure formed by curing the reactive group is more preferred in view of waterproofing. The method for coating the metal oxide surface with a hydrophobic organic material is described, for example, in JP-A-2001-255403 and JP-A-2002-152183. Examples of the coating of a particle with an organic compound having an unsaturated group within the molecule include a method of reacting an acrylic acid ester with a metal compound through an isocyanate to produce an organic compound having at least a metal alkoxide and a reactive unsaturated bond, and surface-treating a metal oxide by using the organic compound. Also, the coating may be performed by making use of a surface treating agent described in JP-A-2001-255403, paragraphs [0039] to [0043]. The term “surface neighborhood” as used herein indicates a region in the depth direction within 500 nm from the particle surface.
Examples of the production method of the light-transparent particle for use in the present invention include a suspension polymerization method, an emulsion polymerization method, a soap-free emulsion polymerization method, a dispersion polymerization method and a seed polymerization method, and the light-transparent particle may be produced by any of these methods. These production methods may be performed by referring to the methods described, for example, in Takayuki Ohtsu and Masaetsu Kinoshita, Kobunshi Gosei no Jikken Ho (Experimental Technique for the Synthesis of Polymer), page 130 and pages 146 to 147, Kagaku Dojin Sha, Gosei Kobunshi (Synthetic Polymer), Vol. 1, pp. 246-290, ibid., Vol. 3, pp. 1-108, U.S. Pat. Nos. 2,543,503, 3,508,304, 2,746,275, 3,521,560 and 3,580,320, JP-A-9-143238, JP-A-10-1561, JP-A-7-2908, JP-A-5-297506, JP-A-2002-145919, JP-A-2003-147039 and JP-A-2003-171432.
In the production method of a melamine resin particle, a benzoguanamine-melamine formaldehyde particle or the like, an insufficiently cured amino resin, that is, a low condensation amino resin, sometimes remains like an impurity after the condensation curing reaction, though the amount thereof is very small, and this incompletely cured amino resin dissolves in a hydrophilic solvent such as water or alcohol conventionally used at the purification such as filtration or classification and disadvantageously precipitates as a coarse particle or an amorphous foreign particle or becomes a viscous residue to aggregate desired amino resin particles or foreign particles and form an aggregated particle. Also, there arises a problem in some cases that the low condensation amino resin brings about a change in the size or shape of the resin particle due to hydrolysis, volatilization, bleed-out or the like under high-temperature high-humidity conditions (specifically, 80° C. and 90% RH) and even a change in the refractive index is caused to vary the light scattering property (deterioration of weather resistance).
As one means for solving these problems, obtaining a high condensation curing degree is exemplified by including a heating step of heating the organic resin particle at a temperature of 100 to 350° C. for 1 to 50 hours in the production of the organic resin particle.
The method for enhancing the condensation curing degree is described below by sequentially describing the steps of producing the amino resin particle. The production process of the amino resin includes the following steps (a) to (d).
(a) a step of subjecting an initial condensate capable of becoming an amino resin to condensation curing in the presence of an acidic catalyst and further subjecting the obtained particle to condensation curing in the presence of an acidic catalyst,
(b) a step of heating the turbid solution obtained in (a) at a temperature of 100 to 350° C. for 1 to 50 hours,
(c) a neutralization step, where the pH value after neutralization is preferably around 7, and
(d) a step of heating the amino resin particle obtained after (c) at a temperature of 100 to 350° C. for 1 to 50 hours.
As for the heat treatment, both steps (b) and (d) may be passed through or only the step (b) or (d) may be sufficient.
Preferred embodiments of the steps (b) and (d) are described below.
In the production method of the present invention, the amino resin particle obtained in the step (a) is heated in an aqueous solution containing a sulfamic acid-based compound and/or an imidazole-based compound at 100° C. or more, preferably 130° C. or more, more preferably 160° C. or more. When this heating is performed at a temperature higher than the boiling point of the aqueous solution, the heating must be performed while pressurizing the inside of a closed vessel such as autoclave. By performing such heating, the condensation curing of the amino resin particle can be made to more proceed and the particle having a desired refractive index can be obtained. If the temperature at the heating above is less than 100° C., the amino resin particle having a desired refractive index may not be obtained.
The sulfamic acid-based compound is not particularly limited, but specific preferred examples thereof include a sulfamic acid (amidosulfuric acid) and a sulfamate(amidosulfate) such as ammonium sulfamate(ammonium amidosulfate) and nickel sulfamate(nickel amidosulfate). The imidazole-based compound is not particularly limited, but specific preferred examples thereof include imidazole, 2-methylimidazole, 4-methylimidazole, 4-methyl-5-(hydroxymethyl)imidazole, 2-amino-4,5-dicyanoimidazole, imidazole-4,5-dicarboxylic acid, 2-ethyl-4-methylimidazole, 2-phenylimidazole, 2-undecylimidazole, 2-heptadecylimidazole, 1-benzyl-2-methylimidazole, 2-phenyl-4-methylimidazole, 1-cyanoethyl-2-methylimidazole and 1-cyanoethyl-2-methylimidazole trimellitate.
The aqueous solution is obtained by incorporating the sulfamic acid-based compound and/or imidazole-based compound into an aqueous medium, and the aqueous medium is not particularly limited, but specific examples of the aqueous medium which can be appropriately used include a water-soluble organic solvent such as alcohol and ketone. The sulfamic acid-based compound and/or imidazole-based compound is preferably added and contained in an amount of 0.5 mass % or more, more preferably from 0.5 to 4 mass %, still more preferably from 1 to 3 mass %, based on the amino resin particle. If the content of such a compound is less than 0.5 mass %, the condensation curing of the amino resin particle may not proceed and the amino resin particle having a desired refractive index may not be obtained.
The heating time in the aqueous solution is not particularly limited, but the specific heating time is preferably, for example, from 1 to 50 hours, more preferably from 2 to 30 hours, still more preferably from 2 to 10 hours. If the heating time is less than 1 hour, the condensation curing of the amino resin particle may not proceed and the amino resin particle having a desired refractive index may not be obtained. Incidentally, the sulfamic acid-based compound and/or imidazole-based compound before heating of the aqueous solution may be in a state of being mixed but not dissolved in the aqueous medium and although not particularly limited, the compound is preferably dissolved after the aqueous solution is heated. Also, the heating of the aqueous solution is preferably performed in a nitrogen atmosphere.
After the neutralization step (c), the amino resin particle is once separated from the aqueous solution, and the particle separated is heat-treated at 100° C. or more, preferably 130° C. or more, more preferably 160° C. or more. By performing such a heat treatment, the condensation curing of the amino resin particle can be made to more proceed and the particle having a desired refractive index can be obtained. If the temperature of this heat treatment is less than 100° C., the amino resin particle having a desired refractive index may not be obtained. The separation from the aqueous solution is not particularly limited and may be performed using a conventionally known method. For example, various separation methods such as separation by natural precipitation or centrifugal precipitation and decantation, and separation by filtration may be used. In advance of the separation, a coagulant such as aluminum sulfate may be added to promote the separation.
The method for the heat treatment above is not particularly limited but specifically, a method of heat-treating the separated amino resin particle by using an apparatus such as drier, hot air drier and vacuum (reduced pressure) drier is preferred. The heat treatment time is not particularly limited but specifically, the heat treatment time is, for example, preferably from 1 to 50 hours, more preferably from 2 to 30 hours, still more preferably from 2 to 10 hours. If the heat treatment time is less than 1 hour, insufficient condensation curing of the amino resin particle may result and the particle having a desired refractive index may not be obtained. In the production method of the present invention, although not particularly limited, an amino resin particle is obtained through the above-described process, and the obtained amino resin particle is preferably further subjected to purification and classification. That is, it is preferred to remove impurities other than the desired amino resin particle or uniformalize the amino resin particle in a desired size.
Also, the heating of the amino resin particle here is preferably performed in an inert gas atmosphere having an oxygen concentration of 10 vol % or less.
The amino resin particle of the present invention preferably has a high condensation curing degree from the standpoint of improving the weather resistance in the film under high-temperature high-humidity conditions.
As an index indicative of condensation curing degree, there is exemplified the area ratio of a carbon atom signal derived from —NH—CH2—NH— bond (C(II) bond) to a carbon atom signal derived from —NH—CH2O—CH2—NH— bond (C(I) bond) in the solid 13C-NMR analysis of the amino resin particle.
By virtue of a high condensation curing degree, the refractive index of the particle can be made high, in addition to the improvement of weather resistance, and an amino resin particle having a refractive index of 1.60 or more, preferably 1.62 or more, more preferably from 1.65 to 1.75, can be obtained.
The refractive index of the particle can be determined by the method described in JP-A-2003-147039, paragraph [0041].
In the solid 13C-NMR analysis, the area ratio (NMR area ratio represented by C(II)/C(I)) of a carbon atom signal derived from (C(II) bond) to a carbon atom signal derived from (C(I) bond) is preferably 2 or more, more preferably from 2 to 20, still more preferably from 2 to 10.
The amount of the amino group or methylol group derived from the unreacted portion is of course preferably smaller.
As for the measuring method, the method described in JP-A-2003-171432 may be used.
The index indicative of the condensation curing degree of the organic resin particle includes a compressive modulus, in addition to the above-described signal ratio of NMR, and the compressive modulus is preferably from 500 to 2,500 kg/mm2, more preferably from 800 to 2,000 kg/mm2, still more preferably from 1,000 to 2,000 kg/mm2. Within this range, the organic resin particle can contribute also to the increase in the film hardness, and the particle is less broken due to environmental change. The compressive modulus can be measured as follows.
Using a micro-compression tester (MCTM-200, product name, manufactured by Shimadzu Corp.), one particle is compressed at a compression speed of 0.27 gf/s, and the compressive modulus at 10% compressive deformation is determined according to the following formula:
K=(3/21/2)·F·S−3/2·R−1/2
(wherein F represents the load value (kgf) at 10% compressive deformation of the particle, S represents the compression displacement (mm) at 10% compressive deformation, and R represents a radius (mm) of the particle).
The internal haze and centerline average roughness of the present invention can be achieved by adjusting the refractive index of the binder according to the refractive index of the light-transparent organic resin particle selected from those particles above.
In the case of using a binder (refractive index after curing: 1.50 to 1.53) mainly comprising a trifunctional or greater (meth)acrylate monomer, the refractive index of the organic resin particle is preferably from 1.60 to 1.75, more preferably from 1.62 to 1.75, still more preferably from 1.65 to 1.75.
More specifically, the binder is preferably used in combination with a light-transparent particle comprising a benzoguanamine-melamine formamide particle (refractive index: 1.68) or a melamine formaldehyde particle (refractive index: 1.65), more preferably in combination with a heat-treated melamine resin particle (refractive index: 1.65) of which surface or surface neighborhood is covered with silica.
In the case of using such a light-transparent organic resin particle, an inorganic filler in a size causing no visible light scattering, such as silica, or a dispersant such as organic compound (which may be either a monomer or a polymer), may be added so as to stabilize the dispersion and prevent the precipitation of the particle in the binder or coating solution. As the amount of the inorganic filler added is larger, this is more effective for preventing the precipitation of the light-transparent organic resin particle but gives an adverse effect on the transparency of the coating film. Accordingly, an inorganic filler having a particle diameter of 0.5 μm or less is preferably contained in the binder to an extent not impairing the transparency of the coating film, that is, in an mount of approximately less than 0.1 mass %. The dispersant such as organic compound is preferably added in an amount of 0.1 to 20 mass %, more preferably from 0.1 to 15 mass %, still more preferably from 0.5 to 10 mass %, based on the organic resin particle. If the amount added is less than 0.1 mass %, the effect by the addition on the dispersion stability is insufficient, whereas if it exceeds 20 mass %, the component not contributing to the dispersion stability increases and causes a problem such as bleed-out.
For the purpose of stabilizing the dispersion and preventing the precipitation in the binder or coating solution, the surface of the fine particle used as the additive may be surface-treated. The kind of the surface treating agent is appropriately selected according to the binder or solvent used. The surface treatment amount is preferably from 0.1 to 30 mass %, more preferably from 1 to 25 mass %, still more preferably from 3 to 20 mass %, based on the organic resin particle. If the surface treatment amount is less than 0.1 mass %, this is insufficient for the dispersion stability, whereas if it exceeds 30 mass %, the component not contributing to the surface treatment increases and causes a problem such as bleed-out.
The average particle diameter of the light-transparent organic resin particle is preferably from 0.5 to 10 μm, more preferably from 1 to 8 μm, still more preferably from 1.2 to 6 μm. If the average particle diameter is less than 0.5 μm, the distribution of light scattering angle extends to a wide angle and the character blurring of the display is disadvantageously brought about, whereas if it exceeds 10 μm, the thickness of the layer to which the light-transparent organic resin particle is added must be increased and this causes a problem such as curl or rise in cost.
For obtaining the required light scattering property, two or more kinds of light-transparent particles differing in the particle diameter may be used in combination.
The light-transparent organic resin particle is blended to account for 3 to 40 mass %, preferably from 3 to 30 mass %, more preferably from 5 to 20 mass %, in the entire solid content of the layer to which the light-transparent organic resin particle is added. If the content of the light-transparent organic resin particle is less than 3 mass %, the effect by the addition is insufficient, whereas if it exceeds 40 mass %, there arises a problem such as image blurring or surface clouding or glaring.
As for the particle size distribution of the light-transparent organic resin particle, in view of the control of haze value and diffusing property and the homogeneity of coated surface state, a monodisperse particle, that is, a particle having a uniform particle diameter, is preferred in the present invention. The CV value indicating the uniformity of particle diameter is preferably from 0 to 10%, more preferably from 0 to 8%, still more preferably from 0 to 5%. Also, when a particle having a particle diameter 20% or more larger than the average particle diameter is defined as a coarse particle, the proportion of this coarse particle is preferably 1% or less, more preferably 0.1% or less, still more preferably 0.01% or less, based on the number of all particles. For obtaining a particle having such a particle size distribution, classification after preparation or synthesis reaction is effective and by increasing the number of classifications or elevating the level of classification, the particle having a desired distribution can be obtained.
The classification is preferably performed using a method such as air classification, centrifugal classification, precipitation classification, filtration classification and electrostatic classification.
In the present invention, a low refractive index layer may be provided on the outer side than the hardcoat layer, that is, on the remoter side from the transparent support. The refractive index of the low refractive index layer is preferably set to be lower than the refractive index of the hardcoat layer. If the difference in the refractive index between the low refractive index layer and the hardcoat layer is too small, the antireflectivity is liable to decrease, whereas if the difference is excessively large, the tint of reflected light tends to be intensified.
In the low refractive index layer of the present invention, a fluorine-containing copolymer compound may be preferably used. Examples of the fluorine-containing vinyl monomer include fluoroolefins (e.g., fluoroethylene, vinylidene fluoride, tetrafluoroethylene, hexafluoropropylene), partially or completely fluorinated alkyl ester derivatives of (meth)acrylic acid (e.g., VISCOAT 6FM (trade name, produced by Osaka Organic Chemical Industry Ltd.), R-2020 (trade name, produced by Daikin Industries, Ltd.)), and completely or partially fluorinated vinyl ethers. Among these, perfluoroolefins are preferred, and hexa-fluoropropylene is more preferred in view of refractive index, solubility, transparency, availability and the like. When the compositional ratio of the fluorine-containing vinyl monomer is increased, the refractive index may be lowered but the film strength decreases. In the present invention, the fluorine-containing vinyl monomer is preferably introduced such that the copolymer has a fluorine content of 20 to 60 mass %, more preferably from 25 to 55 mass %, still more preferably from 30 to 50 mass %.
The constituent unit for imparting crosslinking reactivity mainly includes the following units (A), (B) and (C):
(A): a constituent unit obtained by the polymerization of a monomer previously having a self-crosslinking functional group within the molecule, such as glycidyl (meth)acrylate and glycidyl vinyl ether,
(B): a constituent unit obtained by the polymerization of a monomer having a carboxyl group, a hydroxyl group, an amino group, a sulfo group or the like, such as (meth)acrylic acid, methylol(meth)acrylate, hydroxyalkyl(meth)acrylate, allyl acrylate, hydroxyethyl vinyl ether, hydroxybutyl vinyl ether, maleic acid and crotonic acid, and
(C): a constituent unit obtained by reacting a compound having a group capable of reacting with the functional group of (A) or (B) above within the molecule and separately having a crosslinking functional group, with the constituent unit of (A) or (B) above (for example, a constituent unit which can be synthesized by a technique of causing an acrylic acid chloride to act on a hydroxyl group).
In the constituent unit of (C), the crosslinking functional group is preferably a photopolymerizable group. Examples of the photopolymerizable group include a (meth)acryloyl group, an alkenyl group, a cinnamoyl group, a cinnamylideneacetyl group, a benzalacetophenone group, a styrylpyridine group, an α-phenylmaleimide group, a phenyl-azide group, a sulfonylazide group, a carbonylazide group, a diazo group, an o-quinonediazide group, a furylacryloyl group, a coumarin group, a pyrone group, an anthracene group, a benzophenone group, a stilbene group, a dithiocarbamate group, a xanthate group, a 1,2,3-thiadiazole group, a cyclopropene group and an azadioxabicyclo group. Only one of these groups or two or more kinds thereof may be contained. Among these, a (meth)acryloyl group and a cinnamoyl group are preferred, and a (meth)acryloyl group is more preferred.
The specific method for preparing the photopolymerizable group-containing copolymer includes, but is not limited to, the following methods:
a. a method of reacting a (meth)acrylic acid chloride with a crosslinking functional group-containing copolymer having a hydroxyl group, thereby effecting esterification,
b. a method of reacting an isocyanate group-containing (meth)acrylic acid ester with a crosslinking functional group-containing copolymer having a hydroxyl group, thereby effecting urethanization,
c. a method of reacting a (meth)acrylic acid with a crosslinking functional group-containing copolymer having an epoxy group, thereby effecting esterification, and
d. a method of reacting an epoxy group-containing (meth)acrylic acid ester with a crosslinking functional group-containing copolymer having a carboxyl group, thereby effecting esterification.
The amount of the photopolymerizable group introduced can be arbitrarily adjusted and from the standpoint of, for example, stabilizing the coated film surface state, reducing the surface state failure when an inorganic particle is present together, or enhancing the film strength, it is also preferred to leave a fixed amount of carboxyl group, hydroxyl group or the like.
In the copolymer useful for the present invention, in addition to the repeating unit derived from the fluorine-containing vinyl monomer and the repeating unit having a (meth)acryloyl group in the side chain, other vinyl monomers may be appropriately copolymerized from various viewpoints such as adhesion to substrate, Tg (contributing to film hardness) of polymer, solubility in solvent, transparency, slipperiness, dust protection and antifouling property. A plurality of these vinyl monomers may be combined according to the purpose, and these monomers are preferably introduced to account for, in total, from 0 to 65 mol %, more preferably from 0 to 40 mol %, still more preferably from 0 to 30 mol %, in the copolymer.
The vinyl monomer unit which can be used in combination is not particularly limited, and examples thereof include olefins (e.g., ethylene, propylene, isoprene, vinyl chloride, vinylidene chloride), acrylic acid esters (e.g., methyl acrylate, ethyl acrylate, 2-ethylhexyl acrylate, 2-hydroxyethyl acrylate), methacrylic acid esters (e.g., methyl methacrylate, ethyl methacrylate, butyl methacrylate, 2-hydroxyethyl methacrylate), styrene derivatives (e.g., styrene, p-hydroxymethylstyrene, p-methoxystyrene), vinyl ethers (e.g., methyl vinyl ether, ethyl vinyl ether, cyclohexyl vinyl ether, hydroxyethyl vinyl ether, hydroxybutyl vinyl ether), vinyl esters (e.g., vinyl acetate, vinyl propionate, vinyl cinnamate), unsaturated carboxylic acids (e.g., acrylic acid, methacrylic acid, crotonic acid, maleic acid, itaconic acid), acrylamides (e.g., N,N-dimethylacrylamide, N-tert-butylacrylamide, N-cyclohexylacrylamide), methacrylamides (e.g., N,N-dimethylmethacrylamide), and acrylonitrile.
The fluorine-containing polymer particularly useful in the present invention is a random copolymer of a perfluoroolefin and a vinyl ether or vinyl ester. In particular, the fluorine-containing polymer preferably has a group capable of undergoing a crosslinking reaction by itself (for example, a radical reactive group such as (meth)acryloyl group, or a ring-opening polymerizable group such as epoxy group and oxetanyl group). The crosslinking reactive group-containing polymerization unit preferably occupies from 5 to 70 mol %, more preferably from 30 to 60 mol %, in all polymerization units of the polymer. Preferred examples of the polymer include those described in JP-A-2002-243907, JP-A-2002-372601, JP-A-2003-26732, JP-A-2003-222702, JP-A-2003-294911, JP-A-2003-329804, JP-A-2004-4444 and JP-A-2004-45462.
For the purpose of imparting antifouling property, a polysiloxane structure is preferably introduced into the fluorine-containing polymer for use in the present invention. The method for introducing a polysiloxane structure is not limited, but preferred examples thereof include a method of introducing a polysiloxane block copolymerization component by using a silicone macroazo initiator described in JP-A-6-93100, JP-A-11-189621, JP-A-11-228631 and JP-A-2000-313709, and a method of introducing a polysiloxane graft copolymerization component by using a silicone macromer described in JP-A-2-251555 and JP-A-2-308806. Particularly preferred compounds include the polymers in Examples 1, 2 and 3 of JP-A-11-189621, and Copolymers A-2 and A-3 of JP-A-2-251555. The content of the polysiloxane component in the polymer is preferably from 0.5 to 10 mass %, more preferably from 1 to 5 mass %.
The molecular weight of the polymer which can be preferably used in the present invention is, in terms of the mass average molecular weight, preferably 5,000 or more, more preferably from 10,000 to 500,000, and most preferably from 15,000 to 200,000. It is also possible to improve the coating surface state or scratch resistance by using polymers differing in the average molecular weight in combination.
A curing agent having a polymerizable unsaturated group described in JP-A-10-25388 and JP-A-2000-17028 may be appropriately used in combination with the above-described polymer. Also, as described in JP-A-2002-145952, use in combination with a compound having a fluorine-containing polyfunctional polymerizable unsaturated group is preferred. Examples of the compound having a polyfunctional polymerizable unsaturated group include the polyfunctional monomers described above for the hardcoat layer. Among these compounds, a compound having a polymerizable unsaturated group in the polymer main body is preferred because the combination use of the compound produces a great effect on the improvement of scratch resistance.
The refractive index of the low refractive index layer is preferably from 1.20 to 1.46, more preferably from 1.25 to 1.42, still more preferably from 1.30 to 1.38.
The thickness of the low refractive index layer is preferably from 50 to 150 nm, more preferably from 70 to 120 nm.
The fine particle which can be preferably used in the low refractive index layer of the present invention is described below.
The coated amount of the fine particle is preferably from 1 to 100 mg/m2, more preferably from 5 to 80 mg/m2, still more preferably from 10 to 70 mg/m2. If the coated amount is too small, the effect of improving the scratch resistance may decrease, whereas if it is excessively large, fine irregularities may be generated on the low refractive index layer surface to deteriorate the outer appearance or integrated reflectance. The fine particle is incorporated into the low refractive index layer and therefore, preferably has a low refractive index.
Specifically, a metal oxide fine particle, hollow metal oxide fine particle or hollow organic resin fine particle having a low refractive index is preferred. Examples thereof include a silica fine particle and a hollow silica fine particle. The average particle diameter of the fine particle for use in the low refractive index layer is preferably from 15 to 150%, more preferably from 25 to 100%, still more preferably from 35 to 70%, of the thickness of the low refractive index layer. In other words, when the thickness of the low refractive index layer is 100 nm, the particle diameter of the fine particle is preferably from 15 to 150 nm, more preferably from 25 to 100 nm, still more preferably from 35 to 60 nm. For increasing the scratch resistance, a metal oxide particle is preferably contained in all layers of the optical film, and it is most preferred that a silica particle is contained in all layers of the optical film.
As described above, if the particle diameter of the (hollow) silica fine particle is too small, the effect of improving the scratch resistance may decrease, whereas if it is excessively large, fine irregularities may be generated on the low refractive index layer surface to deteriorate the outer appearance or integrated reflectance. The (hollow) silica fine particle may be either crystalline or amorphous and may be a monodisperse particle or an aggregated particle (in this case, the secondary particle diameter is preferably from 15 to 150% of the thickness of the low refractive index layer). Also, a plurality of two or more kinds of particles (differing in the kind or particle diameter) may be used. The shape is most preferably spherical but even if an indefinite form, there arises no problem.
In order to reduce the refractive index of the low refractive index layer, a hollow silica fine particle is preferably used. The refractive index of the hollow silica fine particle is preferably from 1.17 to 1.40, more preferably from 1.17 to 1.35, still more preferably from 1.17 to 1.30. The refractive index as used herein indicates the refractive index of the particle as a whole and does not indicate the refractive index of only the outer shell silica forming the hollow silica fine particle. At this time, assuming that the radius of the cavity inside the particle is a and the radius of the outer shell of the particle is b, the porosity x is calculated according to the following mathematical formula (I):
x=(4πa3/3)/(4πb3/3)×100 (Mathematical Formula I):
The porosity x is preferably from 10 to 60%, more preferably from 20 to 60%, and most preferably from 30 to 60%. If the hollow silica particle is made to have a lower refractive index and a higher porosity, the thickness of the outer shell becomes small and the strength as a particle decreases. Therefore, in view of the scratch resistance, a particle having a low refractive index of less than 1.17 is not usable. Incidentally, the refractive index of the hollow silica particle was measured by an Abbe refractometer (manufactured by ATAGO K.K.).
In the present invention, from the standpoint of enhancing the antifouling property, the surface free energy on the low refractive index layer surface is preferably reduced. Specifically, a fluorine-containing compound or a compound having a polysiloxane structure is preferably used in the low refractive index layer.
As for the additive having a polysiloxane structure, addition of a reactive group-containing polysiloxane (for example, KF-100T, X-22-169AS, KF-102, X-22-3701IE, X-22-164B, X-22-5002, X-22-173B, X-22-174D, X-22-167B, X-22-161AS (trade names, all produced by Shin-Etsu Chemical Co., Ltd.), AK-5, AK-30, AK-32 (trade names, all produced by Toagosei Chemical Industry Co., Ltd.), SILAPLANE FM0725, SILAPLANE FM0721 (trade names, both produced by Chisso Corp.)) is also preferred. Furthermore, the silicone-based compounds described in Tables 2 and 3 of JP-A-2003-112383 may also be preferably used. Such a polysiloxane is preferably added in an amount of 0.1 to 10 mass %, more preferably from 1 to 5 mass %, based on the entire solid content of the low refractive index layer.
In the optical film of the present invention, a basic compound is preferably added to at least one layer out of the hardcoat layer and the low refractive index layer for improving the weather resistance of the optical film containing the organic resin particle having a refractive index of 1.60 or more. Particularly, when the organic resin particle is an amino resin, acid hydrolysis is readily brought about under high-temperature high-humidity conditions (specifically, 80° C. and 90% RH) and a basic compound is considered to be effective in preventing the acid hydrolysis. The basic compound is not particularly limited as long as it is stably present in the film, but is preferably a primary to quaternary amine, more preferably a tertiary or quaternary amine, still more preferably a quaternary amine (e.g., quaternary ammonium cation structure).
Specific examples of the basic compound include a compound having a polymerizable functional group, such as (meth)acryloylmorpholine, N-vinyl-2-pyrrolidone and N-vinyl-ε-caprolactam, and polymer-type quaternary ammonium salts described in paragraph [0021] of JP-A-2005-316428. Examples of the commercially available quaternary ammonium salt include F-COL 70 [produced by Matsumoto Yushi-Seiyaku Co., Ltd.], TB-34 [produced by Matsumoto Yushi-Seiyaku Co., Ltd.] and Staticide [produced by Mitsui Bussan Plastics Co., Ltd.].
In the present invention, when the basic compound is added to the hardcoat layer containing the organic particle, this is more effective than the addition to the low refractive index layer. However, use in the hardcoat layer has an adverse effect on the dispersion•aggregation state of particles and therefore, the basic compound may be added to the low refractive index layer. The reason why the basic compound is effective even when used in the layer not containing the organic particle is considered because the basic compound diffuses in the film or the acid component of promoting the acid hydrolysis diffuses into the basic compound-containing layer, as a result, the acid catalyst concentration in the vicinity of the particle decreases.
The amount of the basic compound added is, in the case of using the basic compound in the same layer as the organic particle, preferably from 1 to 10 mass %, more preferably from 1 to 5 mass %, and in the case of addition to the layer not containing the organic particle, preferably from 1 to 20 mass %, more preferably from 4 to 15 mass %. (Organosilane Compound)
In view of scratch resistance, at least one layer out of the layers constituting the optical film of the present invention preferably contains at least one component, so-called sol component (hereinafter, sometimes referred to in this way), selected from a hydrolysate of an organosilane compound and/or a partial condensate of the hydrolysate. Particularly, in the case of an optical film having a low refractive index layer, the sol component is preferably incorporated into the low refractive index layer so as to satisfy both the antireflection performance and the scratch resistance. This sol component forms a cured product by undergoing condensation during drying and heating after coating and works out to a part of the binder in the low refractive index layer. Furthermore, in the case where the cured product has a polymerizable unsaturated bond, a binder having a three-dimensional structure is formed upon irradiation with actinic rays.
The organosilane compound is preferably an organosilane compound represented by the following formula 1:
(R1)m-Si(X)4-m Formula 1:
In formula 1, R1 represents a substituted or unsubstituted alkyl group or a substituted or unsubstituted aryl group. The alkyl group is preferably an alkyl group having a carbon number of 1 to 30, more preferably from 1 to 16, still more preferably from 1 to 6. Specific examples of the alkyl group include methyl, ethyl, propyl, isopropyl, hexyl, decyl and hexadecyl. Examples of the aryl group include phenyl and naphthyl, with a phenyl group being preferred.
X represents a hydroxyl group or a hydrolyzable group, and examples thereof include an alkoxy group (preferably an alkoxy group having a carbon number of 1 to 5, e.g., methoxy, ethoxy), a halogen atom (e.g., Cl, Br, I) and a group represented by R2COO (wherein R2 is preferably a hydrogen atom or an alkyl group having a carbon number of 1 to 6; e.g., CH3COO, C2H5COO). Among these, an alkoxy group is preferred, and a methoxy group and an ethoxy group are more preferred.
m represents an integer of 1 to 3 and is preferably 1 or 2.
When a plurality of X's are present, the plurality of X's may be the same or different. The substituent contained in R1 is not particularly limited, but examples thereof include a halogen atom (e.g., fluorine, chlorine, bromine), a hydroxyl group, a mercapto group, a carboxyl group, an epoxy group, an alkyl group (e.g., methyl, ethyl, i-propyl, propyl, tert-butyl), an aryl group (e.g., phenyl, naphthyl), an aromatic heterocyclic group (e.g., furyl, pyrazolyl, pyridyl), an alkoxy group (e.g., methoxy, ethoxy, i-propoxy, hexyloxy), an aryloxy group (e.g., phenoxy), an alkylthio group (e.g., methylthio, ethylthio), an arylthio group (e.g., phenylthio), an alkenyl group (e.g., vinyl, 1-propenyl), an acyloxy group (e.g., acetoxy, acryloyloxy, methacryloyloxy), an alkoxycarbonyl group (e.g., methoxycarbonyl, ethoxycarbonyl), an aryloxycarbonyl group (e.g., phenoxycarbonyl), a carbamoyl group (e.g., carbamoyl, N-methylcarbamoyl, N,N-dimethylcarbamoyl, N-methyl-N-octylcarbamoyl), and an acylamino group (e.g., acetylamino, benzoylamino, acrylamino, methacrylamino). These substituents each may be further substituted.
R1 is preferably a substituted alkyl group or a substituted aryl group.
An organosilane compound having a vinyl polymerizable substituent represented by the following formula 2 is also preferred.
In formula 2, R2 represents a hydrogen atom, a methyl group, a methoxy group, an alkoxycarbonyl group, a cyano group, a fluorine atom or a chlorine atom. Examples of the alkoxycarbonyl group include a methoxycarbonyl group and an ethoxycarbonyl group. R2 is preferably a hydrogen atom, a methyl group, a methoxy group, a methoxycarbonyl group, a cyano group, a fluorine atom or a chlorine atom, more preferably a hydrogen atom, a methyl group, a methoxycarbonyl group, a fluorine atom or a chlorine atom, still more preferably a hydrogen atom or a methyl group.
Y represents a single bond, *—COO—**, *—CONH—** or *—O—** and is preferably a single bond, *—COO—** or *—CONH—**, more preferably a single bond or *—COO—**, still more preferably *—COO—**. * denotes the position bonded to ═C(R2)— and ** denotes the position bonded to L.
L represents a divalent linking chain. Specific examples thereof include a substituted or unsubstituted alkylene group, a substituted or unsubstituted arylene group, a substituted or unsubstituted alkylene group having in the inside thereof a linking group (e.g., ether, ester, amido), and a substituted or unsubstituted arylene group having in the inside thereof a linking group. Among these, preferred are a substituted or unsubstituted alkylene group, a substituted or unsubstituted arylene group, and an alkylene group having in the inside thereof a linking group, more preferred are an unsubstituted alkylene group, an unsubstituted arylene group and an alkylene group having in the inside thereof an ether or ester linking group, and still more preferred are an unsubstituted alkylene group and an alkylene group having in the inside thereof an ether or ester linking group. Examples of the substituent include a halogen, a hydroxyl group, a mercapto group, a carboxyl group, an epoxy group, an alkyl group and an aryl group. These substituents each may be further substituted.
l (which represents a number satisfying the mathematical formula: l=100−m) and m each represents a molar ratio. m represents a number of 0 to 50, and m is preferably a number of 0 to 40, more preferably a number of 0 to 30.
R3 to R6 each is preferably a halogen atom, a hydroxyl group, an unsubstituted alkoxy group or an unsubstituted alkyl group. R3 to R5 each is more preferably a chlorine atom, a hydroxyl group or an unsubstituted alkoxy group having a carbon number of 1 to 6, still more preferably a hydroxyl group or an alkoxy group having a carbon number of 1 to 3, yet still more preferably a hydroxyl group or a methoxy group.
R6 represents a hydrogen atom, an alkyl group, an alkoxy group, an alkoxycarbonyl group, a cyano group, a fluorine atom or a chlorine atom. Examples of the alkyl group include a methyl group and an ethyl group; examples of the alkoxy group include a methoxy group and an ethoxy group; and examples of the alkoxycarbonyl group include a methoxycarbonyl group and an ethoxycarbonyl group. R6 is preferably a hydrogen atom, a methyl group, a methoxy group, a methoxycarbonyl group, a cyano group, a fluorine atom or a chlorine atom, more preferably a hydrogen atom, a methyl group, a methoxycarbonyl group, a fluorine atom or a chlorine atom, still more preferably a hydrogen atom or a methyl group. R7 has the same meaning as R1 in formula 1 and is preferably a hydroxyl group or an unsubstituted alkyl group, more preferably a hydroxyl group or an alkyl group having a carbon number of 1 to 3, still more preferably a hydroxyl group or a methyl group.
Two or more kinds of the compounds represented by formula 1 may be used in combination. In particular, the compound of formula 2 is synthesized using at least one kind of the compound of formula 1 as the starting material. Specific examples of the compound represented by formula 1 and the starting material for the compound represented by formula 2 are set forth below, but the present invention is not limited thereto.
Among these, (M-1), (M-2) and (M-25) are preferred as the organosilane containing a polymerizable group.
In order to obtain the effect of the present invention, the content of the vinyl polymerizable group-containing organosilane in the hydrolysate of the organosilane and/or the partial condensate thereof is preferably from 30 to 100 mass %, more preferably from 50 to 100 mass %, still more preferably from 70 to 95 mass %. If the content of the vinyl polymerizable group-containing organosilane is less than 30 mass %, this is disadvantageous in that production of a solid matter, clouding of the liquid, worsening of the pot life or difficult control of the molecular weight (increase of molecular weight) may be caused or when a polymerization treatment is performed, the performance (for example, scratch resistance of antireflection film) may be hardly enhanced due to small content of the polymerizable group. In the synthesis of the compound represented by formula 2, one organosilane containing a vinyl polymerizable group, selected from (M-1) and (M-2), and one organosilane having no vinyl polymerizable group, selected from (M-19) to (M-21) and (M-48), are preferably used in combination each in the above-described amount.
The volatility of at least either the hydrolysate of the organosilane of the present invention or the partial condensate thereof is preferably reduced so as to stabilize the performance of the coated product. Specifically, the volatilization volume per hour at 105° C. is preferably 5 mass % or less, more preferably 3 mass % or less, still more preferably 1 mass % or less.
The sol component for use in the present invention is prepared by the hydrolysis of the above-described organosilane and/or the partial condensation of the hydrolysate.
The hydrolysis and condensation reaction is performed by adding water in an amount of 0.05 to 2.0 mol, preferably from 0.1 to 1.0 mol, per mol of the hydrolyzable group (X) and stirring the resulting solution at 25 to 100° C. in the presence of a catalyst for use in the present invention.
In at least either the hydrolysate of the organosilane of the present invention or the partial condensate thereof, either the hydrolysate of the vinyl polymerizable group-containing organosilane or the partial condensate thereof preferably has a weight average molecular weight of 450 to 20,000, more preferably from 500 to 10,000, still more preferably from 550 to 5,000, yet still more preferably from 600 to 3,000, excluding the components having a molecular weight of less than 300.
Out of the components having a molecular weight of 300 or more in the hydrolysate of the organosilane and/or the partial condensate thereof, the content of the components having a molecular weight of more than 20,000 is preferably 10 mass % or less, more preferably 5 mass % or less, still more preferably 3 mass % or less. If this content exceeds 10 mass %, the cured film obtained by curing a curable composition containing such a hydrolysate of the organosilane and/or a partial condensate thereof may have poor transparency or poor adhesion to the substrate.
Here, the weight average molecular weight and the molecular weight are a molecular weight determined by the differential refractometer detection with a solvent THF in a GPC analyzer using a column of TSKgel GMHxL, TSKgel G4000HxL or TSKgel G2000HxL (trade names, all produced by Tosoh Corp.) and expressed in terms of polystyrene. The content is an area % of the peaks in the above-described molecular weight range, assuming that the peak area of the components having a molecular weight of 300 or more is 100%.
The dispersity (weight average molecular weight/number average molecular weight) is preferably from 3.0 to 1.1, more preferably from 2.5 to 1.1, still more preferably from 2.0 to 1.1, yet still more preferably from 1.5 to 1.1.
The state of X in formula 1 being condensed in the form of —OSi can be confirmed by the 29Si-NMR analysis of the hydrolysate of the organosilane of the present invention or the partial condensate thereof.
At this time, assuming that the case where three bonds of Si are condensed in the form of —OSi is (T3), the case where two bonds of Si are condensed in the form of —OSi is (T2), the case where one bond of Si is condensed in the form of —OSi is (T1) and the case where Si is not condensed at all is (T0), the condensation rate α is represented by:
α=(T3×3+T2×2+T1×1)/3/(T3+T2+T1+T0) Mathematical Formula (II):
The condensation rate is preferably from 0.2 to 0.95, more preferably from 0.3 to 0.93, still more preferably from 0.4 to 0.9.
If the condensation rate is less than 0.1, the hydrolysis or condensation proceeds insufficiently and due to increase of the monomer component, insufficient curing results, whereas if it exceeds 0.95, the hydrolysis or condensation excessively proceeds and since the hydrolyzable group is consumed out, the interaction of binder polymer, resin substrate, inorganic fine particle and the like is decreased, as a result, the effect can be hardly obtained even when these are used.
The hydrolysate of the organosilane compound and the partial condensate thereof used in the present invention are described in detail below.
The hydrolysis reaction of the organosilane and the subsequent condensation reaction are generally performed in the presence of a catalyst. Examples of the catalyst include inorganic acids such as hydrochloric acid, sulfuric acid and nitric acid; organic acids such as oxalic acid, acetic acid, butyric acid, maleic acid, citric acid, formic acid, methanesulfonic acid and toluenesulfonic acid; inorganic bases such as sodium hydroxide, potassium hydroxide and ammonia; organic bases such as triethylamine and pyridine; metal alkoxides such as triisopropoxy aluminum, tetrabutoxy zirconium, tetrabutyl titanate and dibutyltin dilaurate; metal chelate compounds with the center metal being a metal such as Zr, Ti or Al; and F-containing compounds such as KF and NH4F.
One of these catalysts may be used alone, or a plurality of species thereof may be used in combination.
The hydrolysis and condensation reaction of the organosilane may be performed without a solvent or in a solvent, but in order to uniformly mix the components, an organic solvent is preferably used. Suitable examples thereof include alcohols, aromatic hydrocarbons, ethers, ketones and esters.
The solvent is preferably a solvent capable of dissolving the organosilane and the catalyst. In view of the process, the organic solvent is preferably used as a coating solution or as a part of the coating solution. The solvent is also preferably a solvent which does not impair the solubility or dispersibility when mixed with other materials such as fluorine-containing polymer.
Examples of the alcohols include a monohydric alcohol and a dihydric alcohol. The monohydric alcohol is preferably a saturated aliphatic alcohol having a carbon number of 1 to 8.
Specific examples of the alcohols include methanol, ethanol, n-propyl alcohol, i-propyl alcohol, n-butyl alcohol, sec-butyl alcohol, tert-butyl alcohol, ethylene glycol, diethylene glycol, triethylene glycol, ethylene glycol monobutyl ether and ethylene glycol acetate monoethyl ether.
Specific examples of the aromatic hydrocarbons include benzene, toluene and xylene. Specific examples of the ethers include tetrahydrofuran and dioxane. Specific examples of the ketones include acetone, methyl ethyl ketone, methyl isobutyl ketone, diisobutyl ketone and cyclohexanone. Specific examples of the esters include ethyl acetate, propyl acetate, butyl acetate and propylene carbonate.
One of these organic solvents may be used alone, or two or more kinds thereof may be used as a mixture. The solid content concentration in the reaction is not particularly limited but is usually from 1 to 100%.
The reaction is performed by adding water in an amount of 0.05 to 2 mol, preferably from 0.1 to 1 mol, per mol of the hydrolyzable group of the organosilane, and stirring the resulting solution at 25 to 100° C. in the presence or absence of the above-described solvent and in the presence of the catalyst.
In the present invention, the hydrolysis is preferably performed by stirring the solution at 25 to 100° C. in the presence of at least one metal chelate compound where an alcohol represented by the formula: R3OH (wherein R3 represents an alkyl group having a carbon number of 1 to 10) and a compound represented by the formula: R4COCH2COR5 (wherein R4 represents an alkyl group having a carbon number of 1 to 10 and R5 represents an alkyl group having a carbon number of 1 to 10 or an alkoxy group having a carbon number of 1 to 10) are present as ligands and the center metal is a metal selected from Zr, Ti and Al.
In the case of using a fluorine-containing compound as the catalyst, the fluorine-containing compound has an ability of allowing the progress of complete hydrolysis and condensation and this is advantageous in that the polymerization degree can be determined by selecting the amount of water added and an arbitrary molecular weight can be designed. That is, in order to prepare an organosilane hydrolysate/partial condensate having an average polymerization degree of M, this may be attained by using water in an amount of (M-1) mol per M mol of the hydrolyzable organosilane.
Any metal chelate compound may be suitably used without particular limitation as long as it is a metal chelate compound where an alcohol represented by the formula: R3OH (wherein R3 represents an alkyl group having a carbon number of 1 to 10) and a compound represented by the formula: R4COCH2COR5 (wherein R4 represents an alkyl group having a carbon number of 1 to 10 and R5 represents an alkyl group having a carbon number of 1 to 10 or an alkoxy group having a carbon number of 1 to 10) are present as ligands and the center metal is a metal selected from Zr, Ti and Al. Within this category, two or more kinds of metal chelate compounds may be used in combination. The metal chelate compound for use in the present invention is preferably selected from the group consisting of compounds represented by the formulae: Zr(OR3)p1(R4COCHCOR5)p2, Ti(OR3)q1(R4COCHCOR5)q2 and Al(OR3)r1(R4COCHCOR5)r2. These compounds have an activity of accelerating the condensation reaction of the hydrolysate of the organosilane compound and the partial condensate thereof.
In the metal chelate compounds, R3 and R4 may be the same or different and each represents an alkyl group having a carbon number of 1 to 10, such as ethyl group, n-propyl group, i-propyl group, n-butyl group, sec-butyl group, tert-butyl group, n-pentyl group or phenyl group. R5 represents an alkyl group having a carbon number of 1 to 10 the same as above or an alkoxy group having a carbon number of 1 to 10, such as methoxy group, ethoxy group, n-propoxy group, i-propoxy group, n-butoxy group, sec-butoxy group or tert-butoxy group. In the metal chelate compounds, p1, p2, q1, q2, r1 and r2 each represents an integer determined to satisfy the relationships of p1+p2=4, q1+q2=4 and r1+r2=3.
Specific examples of the metal chelate compound include a zirconium chelate compound such as zirconium tri-n-butoxyethylacetoacetate, zirconium di-n-butoxy-bis-(ethylacetoacetate), zirconium n-butoxytris(ethylacetoacetate), zirconium tetrakis(n-propylacetoacetate), zirconium tetrakis(acetylacetoacetate) and zirconium tetrakis(ethylacetoacetate); a titanium chelate compound such as titanium diisopropoxy•bis(ethylacetoacetate), titanium diisopropoxy•bis(acetylacetate) and titanium diisopropoxy•bis(acetylacetone); and an aluminum chelate compound such as aluminum diisopropoxyethylacetoacetate, aluminum diisopropoxyacetylacetonate, aluminum isopropoxybis(ethylacetoacetate), aluminum isopropoxybis(acetylacetonate), aluminum tris(ethylacetoacetate), aluminum tris(acetylacetonate) and aluminum monoacetyl-acetonate•bis(ethylacetoacetate).
Among these metal chelate compounds, preferred are zirconium tri-n-butoxyethylacetoacetate, titanium diisopropoxybis(acetylacetonate), aluminum diisopropoxyethylacetoacetate and aluminum tris(ethylacetoacetate). One of these meal chelate compounds may be used alone, or two or more kinds thereof may be used as a mixture. A partial hydrolysate of such a metal chelate compound may also be used.
The metal chelate compound is preferably used in a proportion of 0.01 to 50 mass %, more preferably from 0.1 to 50 mass %, still more preferably from 0.5 to 10 mass %, based on the organosilane compound. When the metal chelate compound is used in this range, the condensation reaction of the organosilane compound proceeds at a high rate, the coating film can have good durability, and the composition comprising the hydrolysate of the organosilane compound, the partial condensate thereof and the metal chelate compound is assured of good storage stability.
In the coating solution for use in the present invention, at least either a β-diketone compound or a β-ketoester compound is preferably added in addition to the composition containing the above-described sol component and metal chelate compound. This is described below.
The compound used in the present invention is at least either a β-diketone compound or a β-ketoester compound, represented by the formula: R4COCH2COR5, and this compound functions as a stability enhancer for the composition used in the present invention. That is, this compound is considered to coordinate to a metal atom in the metal chelate compound (at lease any one compound of zirconium, titanium and aluminum compounds) and inhibit the metal chelate compound from exerting the activity of accelerating the condensation reaction of the hydrolysate of the organosilane compound and its partial condensate, thereby acting to enhance the storage stability of the composition obtained. R4 and R5 constituting the β-diketone compound and β-ketoester compound have the same meanings as R4 and R5 constituting the metal chelate compound above.
Specific examples of the β-diketone compound and the β-ketoester compound include acetylacetone, methyl acetoacetate, ethyl acetoacetate, n-propyl acetoacetate, i-propyl acetoacetate, n-butyl acetoacetate, sec-butyl acetoacetate, tert-butyl acetoacetate, 2,4-hexane-dione, 2,4-heptane-dione, 3,5-heptane-dione, 2,4-octane-dione, 2,4-nonane-dione and 5-methyl-hexane-dione. Among these, ethyl acetoacetate and acetylacetone are preferred, and acetylacetone is more preferred. One of these β-diketone compounds and β-ketoester compounds may be used alone, or two or more kinds thereof may be used as a mixture. In the present invention, the β-diketone compound and the β-ketoester compound each is preferably used in an amount of 2 mol or more, more preferably from 3 to 20 mol, per mol of the metal chelate compound. If the amount added is less than 2 mol, the composition obtained may suffer from poor storage stability and this is not preferred.
The content of the hydrolysate of the organosilane compound or the partial condensate thereof is preferably small in the case of an antireflection layer which is a relatively thin film, and preferably large in the case of a hardcoat or antiglare layer which is a thick film. Considering the expression of effect, refractive index, shape/surface state of film and the like, the content is preferably from 0.1 to 50 mass %, more preferably from 0.5 to 30 mass %, and most preferably from 1 to 15 mass %, based on the entire solid content of the layer containing the hydrolysate of the organosilane compound or the partial condensate thereof (the layer to which the hydrolysate of the organosilane compound or the partial condensate thereof is added).
In the case of using the hydrolysate of the vinyl polymerizable group-containing organosilane compound and/or the partial condensate thereof, a photolyzable initiator is preferably used in combination. Examples of the skeleton of such an initiator include the compounds exemplified in the paragraphs of initiator which is described later.
Examples of the photoradical polymerization initiator include acetophenones, benzoins, benzophenones, phosphine oxides, ketals, anthraquinones, thioxanthones, azo compounds, peroxides (see, for example, JP-A-2001-139663), 2,3-dialkyldione compounds, disulfide compounds, fluoroamine compounds, aromatic sulfoniums, lophine dimers, onium salts, borate salts, active esters, active halogens, inorganic complexes and coumarins.
Examples of the acetophenones include 2,2-dimethoxyacetophenone, 2,2-diethoxyacetophenone, p-dimethylacetophenone, 1-hydroxy-dimethyl phenyl ketone, 1-hydroxy-dimethyl-p-isopropyl phenyl ketone, 1-hydroxycyclohexyl phenyl ketone, 2-methyl-4-methylthio-2-morpholinopropiophenone, 2-benzyl-2-dimethylamino-1-(4-morpholinophenyl)-butanone, 4-phenoxydichloroacetophenone and 4-tert-butyl-dichloroacetophenone.
Examples of the benzoins include benzoin, benzoin methyl ether, benzoin ethyl ether, benzoin isopropyl ether, benzyl dimethyl ketal, benzoin benzenesulfonic acid ester, benzoin toluenesulfonic acid ester, benzoin methyl ether, benzoin ethyl ether and benzoin isopropyl ether. Examples of the benzophenones include benzophenone, hydroxybenzophenone, 4-benzoyl-4′-methyldiphenyl sulfide, 2,4-dichlorobenzophenone, 4,4-dichlorobenzophenone, p-chlorobenzophenone, 4,4′-dimethylaminobenzophenone (Michler's ketone) and 3,3′,4,4′-tetra(tert-butylperoxycarbonyl)benzophenone.
Examples of the borate salts include organoborate salt compounds described in Japanese Patent 2764769, JP-A-2002-116539, and Kunz, Martin, Rad Tech' 98, Proceeding April, pages 19-22, 1998, Chicago. More specifically, examples thereof include compounds described in paragraphs [0022] to [0027] of JP-A-2002-116539, supra. Other examples of the organoboron compound include organoboron transition metal coordination complexes described in JP-A-6-348011, JP-A-7-128785, JP-A-7-140589, JP-A-7-306527 and JP-A-7-292014, and specific examples thereof include ion complexes with a cationic coloring matter.
Examples of the phosphine oxides include 2,4,6-trimethylbenzoyldiphenylphosphine oxide.
Examples of the active esters include 1,2-octanedione, 1-[4-(phenylthio)-2-(O-benzoyloxime)], sulfonic acid esters and cyclic active ester compounds.
Specifically, Compounds 1 to 21 described in Examples of JP-A-2000-80068 are preferred.
Examples of the onium salts include an aromatic diazonium salt, an aromatic iodonium salt and an aromatic sulfonium salt.
Specific examples of the active halogens include the compounds described in Wakabayashi et al., Bull Chem. Soc. Japan, Vol. 42, page 2924 (1969), U.S. Pat. No. 3,905,815, JP-A-5-27830, and M. P. Hutt, Journal of Heterocyclic Chemistry, Vol. 1 (No. 3) (1970), particularly a trihalomethyl group-substituted oxazole compound and an s-triazine compound. Among these, preferred is an s-triazine derivative where at least one mono-, di- or tri-halogen-substituted methyl group is bonded to the s-triazine ring. Specifically, s-triazine and oxathiazole compounds are known, and examples thereof include 2-(p-methoxyphenyl)-4,6-bis(trichloromethyl)-s-triazine, 2-(p-styrylphenyl)-4,6-bis(trichloromethyl)-s-triazine, 2-(3-Br-4-di(ethyl acetate)amino)phenyl-4,6-bis(trichloromethyl)-s-triazine and 2-trihalomethyl-5-(p-methoxyphenyl)-1,3,4-oxadiazole. Specific preferred examples thereof include the compounds described at pp. 14-30 of JP-A-58-15503 and pp. 6-10 of JP-A-55-77742, Compound Nos. 1 to 8 described at page 287 of JP-B-60-27673 (the term “JP-B” as used herein means an “examined Japanese patent publication”), Compound Nos. 1 to 17 described at pp. 443-444 of JP-A-60-239736, and Compound Nos. 1 to 19 described in U.S. Pat. No. 4,701,399.
Specific examples of the active halogens are set forth below.
Examples of the inorganic complexes include bis-(η5-2,4-cyclopentadien-1-yl)-bis(2,6-difluoro-3-(1H-pyrrol-1-yl)-phenyl)titanium.
Examples of the coumarins include 3-ketocoumarin.
These initiators may be used individually or as a mixture.
Various examples are also described in Saishin UV Koka Gijutsu (Latest UV Curing Technologies), page 159, Technical Information Institute Co., Ltd. (1991), and Kiyomi Kato, Shigaisen Koka System (Ultraviolet Curing System), pp. 65-148, Sogo Gijutsu Center (1989), and these are useful in the present invention.
Preferred examples of the commercially available photoradical polymerization initiator include KAYACURE (e.g., DETX-S, BP-100, BDMK, CTX, BMS, 2-EAQ, ABQ, CPTX, EPD, ITX, QTX, BTC, MCA) produced by Nippon Kayaku Co., Ltd.; Irgacure (e.g., 651, 184, 500, 819, 907, 369, 1173, 1870, 2959, 4265, 4263) produced by Ciba Specialty Chemicals Corp.; Esacure (KIP100F, KB1, EB3, BP, X33, KT046, KT37, KIP150, TZT) produced by Sartomer Company Inc.; and a mixture thereof.
The photopolymerization initiator is preferably used in an amount of 0.1 to 15 parts by mass, more preferably from 1 to 10 parts by mass, per 100 parts by mass of the polyfunctional monomer.
In addition to the photopolymerization initiator, a photosensitizer may be used. Specific examples of the photosensitizer include n-butylamine, triethylamine, tri-n-butylphosphine, Michler's ketone and thioxanthone.
Furthermore, one or more auxiliary agents such as azide compound, thiourea compound and mercapto compound may be used in combination.
Examples of the commercially available photosensitizer include KAYACURE (DMBI, EPA) produced by Nippon Kayaku Co., Ltd.
As for the thermal radical initiator, an organic or inorganic peroxide, an organic azo or diazo compound, and the like may be used.
More specifically, examples of the organic peroxide include benzoyl peroxide, halogen benzoyl peroxide, lauroyl peroxide, acetyl peroxide, dibutyl peroxide, cumene hydroperoxide and butyl hydroperoxide; examples of the inorganic peroxide include hydrogen peroxide, ammonium persulfate and potassium persulfate; examples of the azo compound include 2,2′-azobis(isobutyronitrile), 2,2′-azobis(propionitrile) and 1,1′-azobis(cyclohexanecarbonitrile); and examples of the diazo compound include diazoaminobenzene and p-nitrobenzenediazonium.
In the case where the monomer or polymer binder constituting the present invention lacks satisfactory curability by itself, the necessary curability can be imparted by blending a crosslinking compound. Particularly, it is effective to incorporate a crosslinking compound into the low refractive index layer.
For example, when the polymer body contains a hydroxyl group, various amino compounds are preferably used as the curing agent. The amino compound used as the crosslinking compound is, for example, a compound having two or more groups in total of either one or both of a hydroxyalkylamino group and an alkoxyalkylamino group, and specific examples thereof include a melamine-based compound, a urea-based compound, a benzoguanamine-based compound and a glycoluril-based compound.
The melamine-based compound is generally known as a compound having a skeleton of a nitrogen atom being bonded to the triazine ring, and specific examples thereof include melamine, alkylated melamine, methylol melamine and alkoxylated methyl melamine. A compound having two or more groups in total of either one or both of a methylol group and an alkoxylated methyl group within one molecule is preferred. Specifically, a methylolated melamine obtained by reacting melamine and formaldehyde under basic conditions, an alkoxylated methyl melamine, and a derivative thereof are preferred, and an alkoxylated methyl melamine is more preferred because good storage stability of the curable resin composition and good reactivity are obtained. The methylolated melamine and alkoxylated methyl melamine used as the crosslinking compound are not particularly limited, and various resinous materials obtained by the method described, for example, in Plastic Zairyo Koza (Plastic Material Course) [8] Urea-Melamine Jushi (Urea-Melamine Resin), Nikkan Kogyo Shinbun-Sha, can also be used.
Examples of the urea-based compound include, in addition to urea, a polymethylolated urea and its derivative such as alkoxylated methylurea and urone ring-containing methylolated urone or alkoxylated methylurone. Also as for the compound such as urea derivative, various resinous materials described in the publication above can be used.
In the film of the present invention, a curing catalyst capable of generating a radical or an acid upon irradiation with ionizing radiation or heat can be used as the curing catalyst for accelerating the curing.
As one example of the optical film of the present invention, the film can be cured by heating and thereby causing a crosslinking reaction between the hydroxyl group of the fluorine-containing compound and a curing agent capable of crosslinking with the hydroxyl group. In this system, the curing is accelerated by an acid and therefore, an acidic substance is preferably added to the curable resin composition. However, if a normal acid is added, the crosslinking reaction proceeds even in the coating solution and this may give rise to a failure (e.g., unevenness, repelling). Accordingly, in order to satisfy both the storage stability and the curing activity in the thermal curing system, it is more preferred that a compound capable of generating an acid under heating is added as the curing catalyst.
The curing catalyst is preferably a salt comprising an acid and an organic base. Examples of the acid include an organic acid such as sulfonic acid, phosphonic acid and carboxylic acid, and an inorganic acid such as sulfuric acid and phosphoric acid. In view of compatibility with the polymer, an organic acid is more preferred, a sulfonic acid and a phosphonic acid are still more preferred, and a sulfonic acid is most preferred. Preferred examples of the sulfonic acid include p-toluenesulfonic acid (PTS), benzenesulfonic acid (BS), p-dodecylbenzenesulfonic acid (DBS), p-chlorobenzenesulfonic acid (CBS), 1,4-naphthalene-disulfonic acid (NDS), methanesulfonic acid (MsOH) and nonafluorobutane-1-sulfonic acid (NFBS), and these all can be preferably used (abbreviations are shown in parentheses).
The curing catalyst greatly varies depending on the basicity and boiling point of the organic base combined with the acid. The curing catalysts preferably used in the present invention from respective standpoints are described below.
As the basicity of the organic base is lower, the acid generation efficiency at the heating is higher and this is preferred in view of curing activity, but if the basicity is too low, the storage stability becomes insufficient. Accordingly, an organic base having appropriate basicity is preferably used. When pKa of the conjugated acid is used as an index indicative of basicity, the pKa of the organic base for use in the present invention is preferably from 5.0 to 11.0, more preferably from 6.0 to 10.5, still more preferably from 6.5 to 10.0. As for the pKa value of the organic base, the values in an aqueous solution are described in Kagaku Binran (Chemical Handbook), Kiso-Hen (Basic Edition), 5th rev., Vol. 2, pp. II-334 to 340, compiled by The Chemical Society of Japan, Maruzene (2004), and an organic base having an appropriate pKa can be selected therefrom. Even when not described in this publication, a compound estimated to have an appropriate pKa from its structure can also be preferably used. Compounds having an appropriate pKa described in the publication above are shown in Table 1 below, but the compounds which can be preferably used in the present invention are not limited thereto.
As the boiling point of the organic base is lower, the acid generation efficiency at the heating is higher and this is preferred in view of curing activity. Accordingly, an organic base having an appropriate boiling point is preferably used. The boiling point of the base is preferably 120° C. or less, more preferably 80° C. or less, still more preferably 70° C. or less.
Examples of the organic base which can be preferably used in the present invention include, but are not limited to, the following compounds. The boiling points are shown in parentheses.
b-3: pyridine (115° C.), b-14: 4-methylmorpholine (115° C.), b-20: diallylmethylamine (111° C.), b-19: triethylamine (88.8° C.), b-21: tert-butylmethylamine (67 to 69° C.), b-22: dimethylisopropylamine (66° C.), b-23: diethylmethylamine (63 to 65° C.), b-24: dimethylethylamine (36 to 38° C.), and b-18: trimethylamine (3 to 5° C.).
In use as the acid catalyst, a salt comprising the acid and the organic base may be isolated and used or after mixing the acid and the organic base to form a salt in a solution, the solution may be used. For both the acid and the organic base, one species may be used alone or a plurality of species may be mixed and used. In mixing the acid and the organic base, these are preferably mixed such that the equivalent ratio of the acid and the organic base becomes 1:0.9 to 1.5, more preferably 1:0.95 to 1.3, still more preferably 1:1.0 to 1.1.
Examples of the material commercially available as the thermal acid generator include Catalyst 4040, Catalyst 4050, Catalyst 600, Catalyst 602, Catalyst 500 and Catalyst 296-9, all produced by Nihon Cytec Industries Inc.; NACURE series 155, 1051, 5076 and 4054J and, as the block type thereof, NACURE series 2500, 5225, X49-110, 3525 and 4167, all produced by King Industries.
The ratio of the thermal acid generator used is preferably from 0.01 to 10 parts by mass, more preferably from 0.1 to 5 parts by mass, still more preferably from 0.2 to 3 parts by mass, per 100 parts by mass of the curable resin composition. When the amount added is in this range, good storage stability of the curable resin composition and good scratch resistance of the coating film are ensured.
The photoacid generator which can be further used as the photopolymerization initiator is described in detail below.
Examples of the acid generator include known compounds such as photo-initiator for photo-cationic polymerization, photo-decoloring agent for coloring matters, photo-discoloring agent and known acid generator used for microresist or the like, and a mixture thereof. Also, examples of the acid generator include an organic halogenated compound, a disulfone compound and an onium compound. Of these, specific examples of the organohalogen compound and the disulfone compound are the same as those described above for the radical-generating compound.
Examples of the photosensitive acid generator include (1) various onium salts such as iodonium salt, sulfonium salt, phosphonium salt, diazonium salt, ammonium salt and pyridinium salt; (2) sulfone compounds such as β-ketoester, β-sulfonylsulfone and their α-diazo compound; (3) sulfonic acid esters such as alkylsulfonic acid ester, haloalkylsulfonic acid ester, arylsulfonic acid ester and imino sulfonate; (4) sulfonimide compounds; and (5) diazomethane compounds.
Examples of the onium compound include a diazonium salt, an ammonium salt, an iminium salt, a phosphonium salt, an iodonium salt, a sulfonium salt, an arsonium salt and a selenonium salt. Among these, a diazonium salt, an iodonium salt, a sulfonium salt and an iminium salt are preferred in view of photosensitivity for the initiation of photopolymerization, material stability of the compound, and the like. Examples thereof include the compounds described in paragraphs [0058] and [0059] of JP-A-2002-29162.
The proportion of the photosensitive acid generator used is preferably from 0.01 to 10 parts by mass, more preferably from 0.1 to 5 parts by mass, per 100 parts by mass of the curable resin composition.
As for other specific compounds and use methods, those described, for example, in JP-A-2005-43876 can be used.
In the optical film of the present invention, the low refractive index layer can be formed by coating, and the coating solution for forming the low refractive index layer preferably contains, as the film-forming component, at least one kind of a light-transparent resin having an ultraviolet (UV)-curable and/or heat-curable functional group (the light-transparent resin having a ultraviolet (UV)-curable and/or heat-curable functional group is preferably, for example, the fluorine-containing polymer or organosilane compound described above).
Also, in the optical film of the present invention, preferably, the coating solution for forming the low refractive index layer contains at least two or more kinds of light-transparent resins as the film-forming component; more preferably, out of these resins, at least one kind of the light-transparent resin has an ultraviolet (UV)-curable functional group and at least one different kind of the light-transparent resin has a heat-curable functional group; still more preferably, the coating solution for forming the low refractive index layer additionally contains at least one kind of a polymerization initiator and at least one kind of a heat-curable crosslinking agent; and yet still more preferably, the low refractive index layer additionally contains a curing catalyst capable of accelerating the thermal curing (as for the polymerization initiator, heat-curable crosslinking agent and curing catalyst capable of accelerating the thermal curing, those described above can be preferably used).
The value obtained by dividing the total mass of a light-transparent resin having at least an ultraviolet (UV)-curable functional group and at least one kind of a polymerization initiator contained in the coating solution for forming the low refractive index layer, by the total weight of at least one kind of a light-transparent resin having a heat-curable functional group and at least one kind of a heat-curable crosslinking agent is preferably from 0.05 to 0.19 in view of the scratch resistance and cost, more preferably from 0.10 to 0.19, still more preferably from 0.15 to 0.19. If the value is less than 0.05, this is not preferred in view of the scratch resistance, whereas if it exceeds 0.20, the proportion of the UV curing component increases and this requires addition of processing conditions (for example, nitrogen purging at UV curing or elevation of film surface temperature) for increasing the polymerization efficiency at UV curing. The oxygen concentration adjusted by nitrogen purging at UV curing is preferably 1,000 ppm or less, more preferably 500 ppm or less, still more preferably 100 ppm or less, and most preferably 50 ppm or less. The film surface temperature at UV curing is preferably 50° C. or more, more preferably 70° C. or more, still more preferably 90° C. or more. If the temperature is excessively high, the support is softened and a handling (conveyance) failure may occur. Therefore, the upper limit of the temperature is decided by taking into account this failure.
For the purpose of improving the surface state (preventing unevenness), various leveling agents are preferably used in at least one hardcoat layer of the present invention. Similarly, for the purpose of preventing unevenness, various leveling agents are preferably used in the low refractive index layer of the present invention. Specifically, the leveling agent is preferably a fluorine-based leveling agent or a silicone-based leveling agent. In particular, a combination use of both a fluorine-based leveling agent and a silicone-based leveling agent is more preferred, because high ability of preventing unevenness is obtained. It is still more preferred to use a leveling agent in all layers.
Also, the leveling agent is preferably an oligomer or a polymer rather than a low molecular compound. When a leveling agent is added, the leveling agent swiftly undergoes uneven distribution to the surface of the coated liquid film and the leveling agent remains unevenly distributed to the surface even after drying, as a result, the surface energy of the hardcoat layer or low refractive index layer to which the leveling agent is added, decreases due to the leveling agent.
From the standpoint of preventing unevenness of the hardcoat layer, the surface energy of the hardcoat layer is preferably low. The surface energy (γsv, unit: mJ/m2) of the hardcoat layer is an energy-reduced surface tension value (a value obtained by converting the mN/m unit into the mJ/m2 unit) of the antiglare hardcoat layer, and the surface tension is defined as a value γsv (=γsd+γsh) which is the sum of γsd and γsh obtained according to the following simultaneous equations (1) and (2) from respective contact angles θH2O and θCH2I2 for pure water H2O and methylene iodide CH2I2 experimentally determined on the antiglare hardcoat layer by referring to D. K. Owens, J. Appl. Polym. Sci., 13, 1741 (1969). Before the measurement, the sample needs to be subjected to humidity conditioning under predetermined temperature and humidity conditions for a fixed time or more. At this time, the temperature is preferably from 20 to 27° C., the humidity is preferably from 50 to 65 RH %, and the humidity conditioning time is preferably 2 hours or more.
1+cos θH2O=2√γsd(√γH2O
1+cos θCH2I2=2√γsd(√γCH2I2
wherein γH2O
The surface energy of the hardcoat layer is preferably 45 mJ/m2 or less, more preferably from 20 to 45 mJ/m2, still more preferably from 20 to 40 mJ/m2.
By setting the surface energy of the hardcoat layer to 45 mJ/m2 or less, an effect of hardly causing unevenness of the hardcoat layer can be obtained.
However, in the case of further coating an upper layer such as low refractive index layer on the hardcoat layer, the leveling agent is preferably dissolved out into the upper layer. The surface energy of the hardcoat layer after immersing the hardcoat layer with the solvent (e.g., methyl ethyl ketone, methyl isobutyl ketone, toluene, cyclohexanone) of the coating solution for the upper layer on the hardcoat layer and washing it out is preferably rather high. The surface energy here is preferably from 35 to 70 mJ/m2.
The fluorine-based leveling agent preferred as the leveling agent for the hardcoat layer is described below. The silicone-based leveling agent is described later.
The fluorine-based leveling agent is preferably a polymer having a fluoroaliphatic group. Furthermore, the useful polymer is a polymer comprising a repeating unit (polymerization unit) corresponding to the monomer of (i) below, or a copolymer of an acrylic or methacrylic resin comprising a repeating unit (polymerization unit) corresponding to the monomer of (i) below and a repeating unit (polymerization unit) corresponding to the monomer of (ii) below, with a vinyl-based monomer copolymerizable therewith. As for such a monomer, those described in J. Brandrup, Polymer Handbook, 2nd ed., Chapter 2, pp. 1-483, Wiley Interscience (1975) may be used.
Examples thereof include compounds having one addition-polymerizable unsaturated bond selected from an acrylic acid, a methacrylic acid, acrylic acid esters, methacrylic acid esters, acrylamides, methacrylamides, allyl compounds, vinyl ethers and vinyl esters.
(i) Fluoroaliphatic Group-Containing Monomer Represented by the Following Formula A
In formula A, R1 represents a hydrogen atom, a halogen atom or a methyl group and is preferably a hydrogen atom or a methyl group. X represents an oxygen atom, a sulfur atom or —N(R12)— and is preferably an oxygen atom or —N(R12)—, more preferably an oxygen atom. R12 represents a hydrogen atom or an alkyl group having a carbon number of 1 to 8 which may have a substituent, and is preferably a hydrogen atom or an alkyl group having a carbon number of 1 to 4, more preferably a hydrogen atom or a methyl group. Rf represents —CF3 or —CF2H.
In formula A, m represents an integer of 1 to 6 and is preferably an integer of 1 to 3, more preferably 1.
In formula A, n represents an integer of 1 to 11 and is preferably an integer of 1 to 9, more preferably from 1 to 6. Rf is preferably —CF2H.
Also, two or more kinds of polymerization units derived from the fluoroaliphatic group-containing monomer represented by formula A may be contained as constituent components in the fluorine-based polymer.
(ii) Monomer Represented by the Following Formula B, Which is Copolymerizable with (i)
In formula B, R13 represents a hydrogen atom, a halogen atom or a methyl group and is preferably a hydrogen atom or a methyl group. Y represents an oxygen atom, a sulfur atom or —N(R15)— and is preferably an oxygen atom or —N(R15)—, more preferably an oxygen atom. R15 represents a hydrogen atom or an alkyl group having a carbon number of 1 to 8 and is preferably a hydrogen atom or an alkyl group having a carbon number of 1 to 4, more preferably a hydrogen atom or a methyl group.
R14 represents a linear, branched or cyclic alkyl group having a carbon number of 1 to 60 which may have a substituent, or an aromatic group (for example, a phenyl group or a naphthyl group) which may have a substituent. The alkyl group may contain a poly(alkyleneoxy) group. R14 is preferably a linear, branched or cyclic alkyl group having a carbon number of 1 to 20, more preferably a linear or branched alkyl group having a carbon number of 1 to 10. The amount of the fluoroaliphatic group-containing monomer of formula A used for the production of the preferred fluorine-based polymer is 10 mass % or more, preferably 50 mass % or more, more preferably from 70 to 100 mass %, still more preferably from 80 to 100 mass %, based on the entire monomer amount of the fluorine-based polymer.
Specific structure examples of the preferred fluorine-based polymer are set forth below, but the present invention is not limited thereto. In the formulae, the numeral indicates the molar ratio of respective monomer components, and Mw indicates the mass average molecular weight.
The amount of the polymerization unit of the fluoroaliphatic group-containing monomer constituting the fluorine-based polymer is preferably in excess of 10 mass %, more preferably from 50 to 100 mass %, and most preferably from 75 to 100 mass % when it is important to prevent unevenness of the hardcoat layer, or most preferably from 50 to 75 mass % when a low refractive index layer is coated on the hardcoat layer (the amount is based on all polymerization units constituting the fluorine-based polymer).
The silicone-based leveling agent is described below.
Preferred examples of the silicone-based compound include those having a substituent at the terminal and/or in the side chain of a compound chain containing a plurality of dimethylsilyloxy unites as the repeating unit. The compound chain containing dimethylsilyloxy as the repeating unit may contain a structure unit other than dimethylsilyloxy. A plurality of substituents which may be the same or different are preferably present. Preferred examples of the substituent include groups containing a polyether group, an alkyl group, an aryl group, an aryloxy group, an acryloyl group, a methacryloyl group, a vinyl group, an aryl group, a cinnamoyl group, an epoxy group, an oxetanyl group, a hydroxyl group, a fluoroalkyl group, a polyoxyalkylene group, a carboxyl group or an amino group. The molecular weight is not particularly limited but is preferably 100,000 or less, more preferably 50,000 or less, still more preferably from 1,000 to 30,000, and most preferably from 1,000 to 20,000. The silicon atom content of the silicone-based compound is not particularly limited but is preferably 18.0 mass % or more, more preferably from 25.0 to 37.8 mass %, and most preferably from 30.0 to 37.0 mass %. Preferred examples of the silicon-based compound include, but are not limited to, X-22-174DX X-22-2426, X-22-164B, X22-164C, X-22-170DX, X-22-176D and X-22-1821 (all trade names) produced by Shin-Etsu Chemical Co., Ltd.; FM-0725, FM-7725, FM-4421, FM-5521, FM6621 and FM-1121 produced by Chisso Corp.; DMS-U22, RMS-033, RMS-083, UMS-182, DMS-H21, DMS-H31, HMS-301, FMS121, FMS123, FMS131, FMS141 and FMS221 (all trade names) produced by Gelest; SH200, DC11PA, SH28PA, ST80PA, ST86PA, ST97PA, SH550, SH710, L7604, FZ-2105, FZ2123, FZ2162, FZ-2191, FZ2203, FZ-2207, FZ-3704, FZ-3736, FZ-3501, FZ-3789, L-77, L-720, L-7001, L-7002, L-7604, Y-7006, SS-2801, SS-2802, SS-2803, SS-2804 and SS-2805 (all trade names) produced by Dow Corning Toray Co., Ltd.; and TSF400, TSF401, TSF410, TSF433, TSF4450 and TSF4460 (all trade names) produced by GE Toshiba Silicones.
The amount of the fluorine-based leveling agent or silicone-based leveling agent added is preferably from 0.001 to 1.0 mass %, more preferably from 0.01 to 0.2 mass %, based on the coating solution.
For reducing the dry unevenness of the low refractive index layer, the solvent of the coating solution for the low refractive index layer of the optical film of the present invention preferably contains a low boiling point solvent having a boiling point of 120° C. or less in an amount of 50 to 100 mass %, preferably from 70 to 100 mass %, more preferably from 90 to 100 mass %, based on the entire mass of the solvent of the coating solution for the low refractive index layer. By virtue of changing as above the solvent composition for the low refractive index layer of the sample according to the present invention, which is described later, the effect was confirmed in the surface state evaluation of the low refractive index layer. Specific representative examples of the solvent of the coating solution are methyl ethyl ketone, methyl isobutyl ketone and toluene, each ensuring good solubility of the fluorine-containing polymer in the low refractive index layer.
In the hardcoat layer, a thickening agent may be used for adjusting the viscosity of the coating solution.
By increasing the viscosity, precipitation of the particle contained may be suppressed or the unevenness-preventing effect may be expected. The thickening agent as used herein means a substance which causes increase in the viscosity of a liquid when added. The increment of viscosity of the coating solution, which is brought about by the addition, is preferably from 0.05 to 50 cP, more preferably from 1 to 50 cP, and most preferably from 2 to 50 cP.
The high molecular polymer used as the thickening agent preferably contains substantially no fluorine atom and/or substantially no silicon atom. The term “substantially” as used herein means that the content of fluorine atom and/or silicon atom is 0.1 mass % or less, preferably 0.01 mass % or less, based on the mass of the high molecular polymer.
The high molecular polymer is preferred as the thickening agent, and specific examples thereof include, but are not limited to, the followings:
polyacrylic acid ester,
polymethacrylic acid ester,
polyvinyl acetate,
polyvinyl propionate,
polyvinyl butyrate,
polyvinylbutyral,
polyvinylformal,
polyvinylacetal,
polyvinylpropanal,
polyvinylhexanal,
polyvinylpyrrolidone,
cellulose acetate,
cellulose propionate, and
cellulose acetate butyrate.
Among these, preferred are a polymethacrylic acid ester (specifically, methyl polymethacrylate and ethyl polymethacrylate), polyvinyl acetate, polyvinyl propionate, cellulose propionate and cellulose acetate butyrate.
The mass average molecular weight of these polymers is preferably from 100,000 to 1,000,000.
Other than these, a known viscosity adjusting agent or thixotropy imparting agent, such as smectite, fluorotetrasilicon mica, bentonite, silica, montmorillonite and sodium polyacrylate described in JP-A-8-325491, and ethyl cellulose, polyacrylic acid and organic clay described in JP-A-10-219136, may be used.
The transparent support for use in the optical film of the present invention is preferably a plastic film. Examples of the polymer for forming the plastic film include a cellulose ester (e.g., triacetyl cellulose, diacetyl cellulose; representatively, TAC-TD80U, TD80UF, etc. produced by Fuji Photo Film Co., Ltd.), a polyamide, a polycarbonate, a polyester (e.g., polyethylene terephthalate, polyethylene naphthalate), a polystyrene, a polyolefin, a norbornene-based resin (ARTON, trade name, produced by JSR Corp.) and an amorphous polyolefin (ZEONEX, trade name, produced by Zeon Corp.). Among these, preferred are triacetyl cellulose, polyethylene terephthalate and polyethylene naphthalate, and more preferred is triacetyl cellulose. Furthermore, a cellulose acylate film substantially free of a halogenated hydrocarbon such as dichloromethane and the production method thereof are described in JIII Journal of Technical Disclosure (No. 2001-1745, issued Mar. 15, 2001; hereinafter simply referred to as Technical Disclosure No. 2001-1745), and the cellulose acylate described therein can also be preferably used in the present invention. The thickness of the support is, in view of response to need for thinning and handling (suitability for conveyance), suitably from 20 to 200 μm, preferably from 30 to 100 μm, more preferably from 35 to 90 μm, and most preferably from 40 to 80 μm.
The width of the support may be arbitrarily selected but in view of response to increase in the size of an image display apparatus, handling (suitability for conveyance), yield and productivity, the width is usually from 100 to 5,000 mm, preferably from 800 to 3,000 mm, more preferably from 1,000 to 2,000 mm.
The internal haze used in the present invention is described in detail below. After adding several silicone oil drops on the front and back surfaces of the optical film, the film is sandwiched front and back by two 1 mm-thick glass plates (Microslide Glass No. S9111, produced by Matsunami K. K.), the haze is measured according to JIS-K7136 in a state of two glass plates being in complete contact with the optical film obtained, and the value obtained by subtracting, from this haze value, the haze separately measured by interposing only the silicone oil between two glass plates is calculated as the internal haze.
The internal haze is preferably from 20 to 95% in view of making less discernable the liquid crystal panel patter, color unevenness, brightness unevenness, glaring and the like or imparting a function of enlarging the viewing angle by the effect of scattering, and the internal haze is more preferably from 35 to 90%, still more preferably 45 to 85%.
Also, the percentage change in the haze after placing the optical film of the present invention in an environment at a temperature of 80° C. and a relative humidity of 90% for 500 hours is preferably 15% or less in view of small change in the light scattering property, more preferably 10% or less, still more preferably 8% or less.
The entire beam transmittance of the optical film of the present invention is measured according to JIS-K7316. The entire beam transmittance is preferably 85% or more in view of front contrast, more preferably 90% or more, still more preferably 92% or more.
Also, the percentage change in the entire beam transmittance after placing the optical film of the present invention in an environment at a temperature of 80° C. and a relative humidity of 90% for 500 hours is preferably 5% or less in view of small change in the light scattering property (particularly, front contrast), more preferably 4% or less, still more preferably 3% or less.
In view of antifouling property, the contact angle for pure water on the surface of the optical film of the present invention as measured in an environment of 25° C. and 60% RH is preferably 90° or more, more preferably 95° or more, still more preferably 100° or more. Also, the change in the contact angle between before and after saponification treatment (described later) required at the processing into a polarizing plate is preferably 5° or less, more preferably 3° or less, and most preferably 1° or less.
In view of dust resistance, the vertical separation charge of the optical film of the present invention for polyethylene terephthalate as measured in an environment of 25° C. and 60% RH is preferably from −500 to +500 pc (pico coulomb)/cm2, more preferably from −200 to +200 pc (pico coulomb)/cm2, still more preferably from −100 to +100 pc (pico coulomb)/cm2. The vertical separation charge is measured as follows.
The measurement sample is previously left standing in an environment of 25° C. and 60% RH for 2 hours or more. The measuring apparatus comprises a stage on which the measurement sample is placed, and a head for holding the other party film, which can repeat the pressing from above to the measurement sample and the separation therefrom. A polyethylene terephthalate is loaded in this head and after removing electricity from the measuring portion, the head is repeatedly pressed to and separated from the measurement sample. The electric charge value is read at the first separation and at the fifth separation, and the obtained values are averaged. By varying the sample, this operation is repeated on three samples. All values are averaged and the obtained value is defined as the vertical separation charge.
In the case of an optical film where at least one member out of the constituent materials of the low refractive index layer comprises a fluorine-containing material, for adjusting the vertical separation charge to fall in the preferred range above, the photoelectron spectral intensity ratio F/C is from 0.5 to 5, preferably from 0.5 to 3, more preferably from 0.5 to 2. Also, for adjusting the vertical separation charge, silicone having high surface orientation property similarly to fluorine is preferably incorporated and in this case, the photoelectron spectral intensity ratio Si/C is from 0.05 to 0.5, preferably from 0.1 to 0.5, more preferably from 0.2 to 0.5. Incidentally, F/C (=F1 s/C1 s) and Si/C (=Si2 p/C1 s) are values measured as follows.
The photoelectron spectra of Si2 p, F1 s and C1 s on the outermost surface of the optical film are measured by ESCA-3400 (degree of vacuum: 1×10−5 Pa, X-ray source: target Mg, voltage: 12 kV, current: 20 mA) manufactured by Shimadzu Corp.
For enhancing the dust resistance, this may be attained by adjusting the surface resistance value of the optical film of the present invention to less than 1×1011 Ω/square, preferably less than 1×1010 Ω/square, more preferably less than 1×109 Ω/square. The measuring method of the surface resistance value is described later. In the optical film of the present invention, various electrically conducting particles may be used so as to impart electrical conductivity. The electrically conducting particle is preferably formed of a metal oxide or nitride. Examples of the metal oxide or nitride include tin oxide, indium oxide, zinc oxide and titanium nitride, with tin oxide and indium oxide being preferred. The electrically conducting inorganic particle comprises such a metal oxide or nitride as the main component and may further contain other elements. The “main component” means a component of which content (mass %) is largest among the components constituting the particle. Examples of the other element include Ti, Zr, Sn, Sb, Cu, Fe, Mn, Pb, Cd, As, Cr, Hg, Zn, Al, Mg, Si, P, S, B, Nb, In, V and a halogen atom. In order to elevate the electrical conductivity of tin oxide or indium oxide, it is preferred to add Sb, P, B, Nb, In, V or a halogen atom. An Sb-containing tin oxide (ATO) and an Sn-containing indium oxide (ITO) are particularly preferred. The proportion of Sb in ATO is preferably from 3 to 20 mass %, and the proportion of Sn in ITO is preferably from 5 to 20 mass %.
The average primary particle diameter of the electrically conducting inorganic particle for use in the antistatic layer is preferably from 1 to 150 nm, more preferably from 5 to 100 nm, and most preferably from 5 to 70 nm. The average particle diameter of the electrically conducting inorganic particle in the antistatic layer formed is from 1 to 200 nm, preferably from 5 to 150 nm, more preferably from 10 to 100 nm, and most preferably from 10 to 80 nm. The average particle diameter of the electrically conducting inorganic particle is an average diameter weighed by the mass of particle and can be measured by a light scattering method or an electron micrograph.
The specific surface area of the electrically conducting inorganic particle is preferably from 10 to 400 m2/g, more preferably from 20 to 200 m2/g, and most preferably from 30 to 150 m2/g.
The electrically conducting inorganic particle may be surface-treated. The surface treatment is performed using an inorganic compound or an organic compound. Examples of the inorganic compound for use in the surface treatment include alumina and silica. A silica treatment is preferred. Examples of the organic compound for use in the surface treatment include a polyol, an alkanolamine, a stearic acid, a silane coupling agent and a titanate coupling agent, with a silane coupling agent being most preferred. Two or more kinds of surface treatments may be practiced in combination.
The shape of the electrically conducting inorganic particle is preferably rice grain-like, spherical, cubic, spindle-like or amorphous.
Two or more kinds of electrically conducting particles may be used in combination in a specific layer or as a film. The proportion of the electrically conducting inorganic particle in the antistatic layer is preferably from 20 to 90 mass %, more preferably from 25 to 85 mass %, still more preferably from 30 to 80 mass %. Also, the electrically conducting inorganic particle can be used in a dispersion state for the formation of the antistatic layer.
As for the measuring method of the surface resistance value, the sample film is previously left standing in an environment of 25° C. and 60% RH for 2 hours or more and thereafter, the surface resistance on the coating layer side is measured by an ultra-insulating resistance/microammeter, TR8601 (manufactured by Advantest Corp.).
The dynamic friction coefficient of the optical film of the present invention is preferably 0.3 or less in view of enhancing the scratch resistance (preventing the stress concentration), more preferably 0.2 or less, still more preferably 0.1 or less. The method of measuring the dynamic friction coefficient is as follows.
The measurement sample is previously left standing in an environment of 25° C. and 60% RH for 2 hours and then measured by a dynamic friction measuring meter, HEIDON-14, with a 5 mmφ stainless steel ball under a load of 100 g at a speed of 60 cm/min, and the obtained value is used.
In the optical film of the present invention, assuming that the average value of 5° specular reflectance in the wavelength region of 450 to 650 nm is A and the average value of integrated reflectance in that region is B, in view of denseness of black display in a bright room environment or enhancement of bright room contrast, B is preferably 3% or less and B-A is preferably 1.5% or less. B is more preferably 2% or less, still more preferably 1% or less, and B-A is more preferably 1% or less, still more preferably 0.5% or less. The average values of 5° specular reflectance and integrated reflectance are measured as follows.
In the measurement of the specular reflectivity, an adapter “ARV-474” is loaded in a spectrophotometer “V-550” [manufactured by JASCO Corp.], the specular reflectivity for the outgoing angle of −5° at an incident angle of 5° is measured in the wavelength region of 380 to 780 nm, and an average specular reflectivity at 450 to 650 nm is calculated. In the measurement of the integrated reflectance, an adapter “ILV-471” is loaded in a spectro-photometer “V-550” [manufactured by JASCO Corp.], the integrated reflectance at an incident angle of 5° is measured in the wavelength region of 380 to 780 nm, and an average integrated reflectance at 450 to 650 nm is calculated.
The optical film of the present invention can be formed by the following method, but the present invention is not limited thereto.
A coating solution containing components for forming each layer is prepared. At this time, the percentage of water content in the coating solution can be prevented from increasing by minimizing the volatilization volume of the solvent. The percentage of water content in the coating solution is preferably 5% or less, more preferably 2% or less. The volatilization volume of the solvent can be suppressed, for example, by enhancing the closeness at the stirring after materials are charged into a tank or by minimizing the contact area of the coating solution with air at the liquid transfer operation. Also, means for reducing the percentage of water content in the coating solution may be provided during, before or after the coating.
The coating solution used for coating is preferably filtered before coating. The filtration is preferably preformed using a filter having a pore size as small as possible within the range of not allowing for elimination of the components in the coating solution. In the filtration, a filter having an absolute filtration accuracy of 0.1 to 50 μm is used. A filter having an absolute filtration accuracy of 0.1 to 40 μm is more preferred. The filter thickness is preferably from 0.1 to 10 mm, more preferably from 0.2 to 2 mm. In this case, the filtration is preferably performed under a filtration pressure of 1.5 MPa or less, more preferably 1.0 MPa or less, still more preferably 0.2 MPa or less.
The filter member for filtration is not particularly limited as long as it does not affect the coating solution. Specific examples thereof are the same as those of the filtration member described above for the wet dispersion of an inorganic compound.
It is also preferred to ultrasonically disperse the filtered coating solution immediately before coating and assist in removing bubbles or keeping the dispersed state of the dispersion.
The support for use in the present invention is preferably subjected, before coating, to a heat treatment for correcting the base deformation or to a surface treatment for improving the coatability or adhesion to the coated layer. Specific examples of the method for surface treatment include a corona discharge treatment, a glow discharge treatment, a flame treatment, an acid treatment, an alkali treatment and an ultraviolet irradiation treatment. It is also preferred to provide an undercoat layer as described in JP-A-7-333433.
Furthermore, examples of the dedusting method for use in the dedusting step as a pre-step before coating include a dry dedusting method such as a method of pressing a nonwoven fabric, a blade or the like against the film surface described in JP-A-59-150571; a method of blowing an air having high cleanliness at a high speed to separate attached matters from the film surface, and sucking these matters through a proximate suction port described in JP-A-10-309553; and a method of blowing a compressed air under ultrasonic vibration to separate attached matters, and sucking these matters described in JP-A-7-333613 (for example, NEW ULTRA-CLEANER manufactured by Shinko Co., Ltd.).
Also, a wet dedusting method may be used, such as a method of introducing the film into a cleaning tank, and separating attached matters by using an ultrasonic vibrator; a method of supplying a cleaning solution to the film, and blowing an air at a high speed, followed by sucking described in JP-B-49-13020; and a method of continuously rubbing the web with a liquid-moistened roll, and jetting a liquid onto the rubbed face, thereby cleaning the web, described in JP-A-2001-38306. Among these dedusting methods, an ultrasonic dedusting method and a wet dedusting method are preferred in view of the dedusting effect.
Before performing such a dedusting step, the static electricity on the film support is preferably destaticized so as to elevate the dedusting efficiency and prevent attachment of dusts. As for the destaticizing method, an ionizer of corona discharge type, an ionizer of light irradiation type (e.g., UV, soft X-ray), and the like may be used. The voltage charged on the film support before and after dedusting and coating is preferably 1,000 V or less, more preferably 300 V or less, still more preferably 100 V or less.
From the standpoint of maintaining the planarity of the film, in these treatments, the temperature of the cellulose acylate film is preferably kept to be Tg or less, specifically 150° C. or less.
In the case of laminating the cellulose acylate film to a polarizing film as in using the film of the present invention for a protective film of a polarizing plate, in view of adhesive property to the polarizing film, an acid or alkali treatment, that is, a saponification treatment for cellulose acylate, is preferably performed.
In view of adhesive property, the surface energy of the cellulose acylate film is preferably 55 mN/m or more, more preferably from 60 to 75 mN/m. The surface energy can be adjusted by the above-described surface treatment.
Each layer of the film of the present invention can be formed by the following coating methods, but the present invention is not limited thereto.
A known method such as dip coating method, air knife coating method, curtain coating method, roller coating method, wire bar coating method, gravure coating method, extrusion coating method (die coating method) (see, U.S. Pat. No. 2,681,294 and WO2005/123274) and microgravure coating method, is used. Among these, a microgravure coating method and a die coating method are preferred.
The microgravure coating method for use in the present invention is a coating method where a gravure roll having a diameter of about 10 to 100 mm, preferably from about 20 to 50 mm, and having a gravure pattern engraved on the entire circumference is rotated under the support in the direction reverse to the support-conveying direction and at the same time, the surplus coating solution is scraped off from the surface of the gravure roll by a doctor blade, thereby allowing a constant amount of the coating solution to be transferred to and coated on the bottom surface of the support at the position where the top surface of the support is in a free state. A roll-form transparent support is continuously unrolled and on one side of the unrolled support, at least one layer of the hardcoat layer and the low refractive index layer containing a fluorine-containing olefin-based polymer can be coated by the microgravure coating method.
As for the coating conditions in the microgravure coating method, the number of lines in the gravure pattern engraved on the gravure roll is preferably from 50 to 800 lines/inch, more preferably from 100 to 300 lines/inch, the depth of the gravure pattern is preferably from 1 to 600 μm, more preferably from 5 to 200 μm, the rotation number of the gravure roll is preferably from 3 to 800 rpm, more preferably from 5 to 200 rpm, and the support-conveying speed is preferably from 0.5 to 100 m/min, more preferably from 1 to 50 m/min.
In order to provide the film of the present invention with high productivity, an extrusion method (die coating method) is preferably used.
The die coating method is a pre-measurement system and therefore, a stable film thickness can be easily ensured. Also, this coating method can apply a low-amount coating solution at a high speed with good film thickness stability. The coating may be performed by other coating methods, but in a dip coating method, the coating solution in a liquid-receiving tank is inevitably vibrated and stepwise unevenness is readily generated. In a reverse roll coating method, stepwise unevenness is liable to occur due to eccentricity or deflection of the roll involved in the coating. Also, these coating methods are a post-measurement system and therefore, a stable film thickness can be hardly ensured. In view of productivity, the coating is preferably performed using the above-described die coating method at a rate of 25 m/min or more.
After coating on the support directly or through another layer, the film of the present invention is preferably conveyed in the form of a web to a heated zone for drying the solvent.
As for the method of drying the solvent, various known techniques may be utilized. Specific examples thereof include those described in JP-A-2001-286817, JP-A-2001-314798, JP-A-2003-126768, JP-A-2003-315505 and JP-A-2004-34002.
The temperature in the drying zone is preferably from 25 to 140° C. and it is preferred that the temperature in the first half of the drying zone is relatively low and the temperature in the second half is relatively high. However, the temperature is preferably not more than a temperature at which the components other than the solvent contained in the coating composition for each layer start volatilizing. For example, some commercially available photoradical generators used in combination with an ultraviolet curable resin volatilize by about several tens of percent within several minutes in warm air at 120° C., and some mono-functional or bifunctional acrylate monomers or the like allow progress of their volatilization in warm air at 100° C. In such a case, as described above, the drying zone temperature is preferably not more than a temperature at which the components other the solvent contained in the coating composition for each layer start volatilizing.
In order to prevent drying unevenness, the drying air after applying the coating composition for each layer on the support is preferably blown at a wind velocity of 0.1 to 2 m/sec on the coating film surface when the solid content concentration of the coating composition is from 1 to 50%.
Also, in the drying zone after applying the coating composition for each layer on the support, the difference in the temperature between the support and a conveying roll in contact with the surface opposite the coated surface of the support is preferably set to be from 0 to 20° C., because drying unevenness due to uneven heat transfer on the conveying roll can be prevented.
The optical film of the present invention after drying the solvent is passed in the form of a web through a zone for curing each coating film by the irradiation of ionizing radiation and/or under heat, whereby the coating film can be cured. The species of the ionizing radiation for use in the present invention is not particularly limited and according to the kind of the curable composition for forming a film, the radiation may be appropriately selected from ultraviolet ray, electron beam, near ultraviolet ray, visible light, near infrared ray, infrared ray, X-ray and the like. Among these, ultraviolet ray and electron beam are preferred, and ultraviolet is more preferred in that the handling is easy and a high energy can be easily obtained.
As regards the light source of emitting ultraviolet ray for photopolymerizing an ultraviolet-reactive compound, any light source may be used as long as it emits an ultraviolet ray. Examples of the light source which can be used include a low-pressure mercury lamp, a medium-pressure mercury lamp, a high-pressure mercury lamp, an ultrahigh-pressure mercury lamp, a carbon arc lamp, a metal halide lamp and a xenon lamp. Also, an ArF excimer laser, a KrF excimer laser, an excimer lamp, a synchrotron radiation light and the like may be used. Among these, an ultrahigh-pressure mercury lamp, a high-pressure mercury lamp, a low-pressure mercury lamp, a carbon arc, a xenon arc and a metal halide lamp can be preferably used.
An electron beam may also be similarly used. Examples of the electron beam include electron beams having an energy of 50 to 1,000 keV, preferably from 100 to 300 keV, emitted from various electron beam accelerators such as Cockroft-Walton type, Van de Graff type, resonance transformer type, insulating core transformer type, linear type, dynamitron type and high frequency type.
The irradiation conditions vary depending on individual lamps, but the amount of light irradiated is preferably 10 mJ/cm2 or more, more preferably from 50 to 10,000 mJ/cm2, still more preferably from 50 to 2,000 mJ/cm2. At this time, the irradiation dose distribution in the web width direction is preferably, including both edges, from 50 to 100%, more preferably from 80 to 100%, based on the maximum irradiation dose in the center.
In the present invention, at least one layer out of layers stacked on the support is preferably cured by a step of irradiating ionizing radiation and at the same time, irradiating the ionizing radiation in an atmosphere having an oxygen concentration of 1,000 ppm or less, preferably 500 ppm or less, more preferably 100 ppm or less, most preferably 50 ppm or less, for 0.5 seconds or more from the initiation of ionizing radiation irradiation in the state of the layer being heated at a film surface temperature of 50° C. or more.
It is also preferred that the layer is heated simultaneously with and/or successively to the irradiation of ionizing radiation, in an atmosphere having a low oxygen concentration.
In particular, the low refractive index layer which is an outermost layer and has a small film thickness is preferably cured by this method. The curing reaction is accelerated by the heat, and a film excellent in the physical strength and chemical resistance can be formed.
The time for which the ionizing radiation is irradiated is preferably from 0.7 to 60 seconds, more preferably from 0.7 to 10 seconds. If the irradiation time is less than 0.5 seconds, the curing reaction cannot be completed and satisfactory curing cannot be performed. Also, it is not preferred to keep the low oxygen condition for a long period of time, because large-scale equipment and a large amount of inert gas are required.
As for the means to reduce the oxygen concentration to 1,000 ppm or less, replacement of the atmospheric air with another gas is preferred, and replacement with nitrogen (nitrogen purging) is more preferred.
When the conditions are set such that the inert gas is supplied to the ionizing radiation irradiation chamber (also referred to as a “reaction chamber”) for performing the curing reaction by ionizing radiation and at the same time, slightly blown out to the web inlet side of the reaction chamber, not only the carry-over air associated with the web conveyance can be eliminated to effectively decrease the oxygen concentration in the reaction chamber but also the substantial oxygen concentration on the extreme surface greatly susceptible to curing inhibition by oxygen can be efficiently reduced. The direction to which the inert gas flows on the web inlet side of the reaction chamber can be controlled by adjusting the balance between air supply and air discharge in the reaction chamber.
Blowing of the inert gas directly on the web surface is also preferred as the method for removing the carry-over air.
Furthermore, when a pre-chamber is provided before the reaction chamber and the oxygen on the web surface is previously eliminated, the curing can be allowed to proceed more efficiently. In order to efficiently use the inert gas, the gap between the side surface constituting the web inlet side of the ionizing radiation reaction chamber or pre-chamber and the web surface is preferably from 0.2 to 15 mm, more preferably from 0.2 to 10 mm, and most preferably from 0.2 to 5 mm. However, for continuously producing the web, the web needs to be joined and spliced and a method of laminating a bonding tape or the like is widely employed for joining. Therefore, when the gap between the inlet surface of the ionizing radiation reaction chamber or pre-chamber and the web is too small, there arises a problem that the bonding member such as bonding tape is hung up. To solve this problem, in the case of forming a narrow gap, at least a part of the inlet surface of the ionizing radiation reaction chamber or pre-chamber is preferably made movable, so that the gap can be enlarged for the thickness of the bonded part when the bonded part enters the chamber. This construction may be realized by a method where the inlet surface of the ionizing radiation reaction chamber or pre-chamber is made movable back and forth in the running direction and moved back and forth to enlarge the gap when the bonded part passes therethrough, or a method where the inlet surface of the ionizing radiation reaction chamber or pre-chamber is made movable perpendicularly to the web surface and moved vertically to enlarge the gap when the bonded part passes therethrough.
The ultraviolet ray may be irradiated every time when a plurality of constituent layers each is formed or may be irradiated after the layers are stacked. Alternatively, some of these layers may be irradiated in combination. In view of productivity, the ultraviolet ray is preferably irradiated after stacking multiple layers.
In the present invention, at least one layer stacked on the support may be cured by irradiating the ionizing radiation a plurality of times. In this case, the irradiation of ionizing radiation is preferably performed at least twice in continuous reaction chambers where the oxygen concentration does not exceed 1,000 ppm. By performing the irradiation of ionizing radiation a plurality of times in reaction chambers having the same low oxygen concentration, the reaction time necessary for curing can be effectively ensured.
Particularly, in the case of elevating the production speed for high productivity, the ionizing radiation needs to be irradiated a plurality of time for ensuring an ionizing radiation energy necessary for the curing reaction.
In the case where the curing percentage (100—percentage of residual functional group content) becomes a certain value less than 100%, when another layer is provided thereon and cured by ionizing radiation and/or under heat, the curing percentage of the lower layer is preferably higher than that before providing the upper layer, because the adhesion between the lower layer and the upper layer is improved.
In order to continuously produce the film of the present invention, a step of continuously feeding a rolled support film, a step of coating and drying the coating solution, a step of curing the coating film, and a step of taking up the support film having thereon the cured layer are performed.
A film support unrolled from a rolled film support is continuously fed to a clean room, static electricity charged to the film support is removed by a destaticizing apparatus in the clean room, and foreign matters adhering to the film support are then removed by a dedusting apparatus. Subsequently, a coating solution is coated on the film support in a coating part disposed in the clean room, and the coated film support is conveyed to a drying room and dried.
The film support having thereon the dried coating layer is delivered from the drying room to a curing room, where the monomer contained in the coating layer is polymerized to effect curing. The film support having thereon the cured layer is further conveyed to a curing part, where the curing is completed, and the film support having thereon the completely cured layer is taken up into a roll.
The above-described steps may be performed every time when each layer is formed, or a plurality of coating part-drying room-curing part lines may be provided to continuously perform the formation of respective layers.
In producing the film of the present invention, it is preferred that in combination with the above-described microfiltration operation of the coating solution, the coating step in the coating part and the drying step in the drying room are performed in an atmosphere having high air cleanliness and dirt and dust on the film are satisfactorily removed before performing the coating. The air cleanliness in the coating step and drying step is, according to the standard of air cleanliness in US Federal Standard 209E, preferably not lower than class 10 (the number of particles of 0.5 μm or more is 353 per (cubic meter) or less), more preferably not lower than class 1 (the number of particles of 0.5 μm or more is 35.5 per (cubic meter) or less). The air cleanliness is preferably high also in the parts other than the coating-drying steps, such as delivery part and take-up part.
In producing a polarizing plate by using the film of the present invention for one film out of two surface protective films of a polarizing film, the surface on the side to be laminated with the polarizing film is preferably hydrophilized to improve the adhesive property on the bonding surface.
a. Method by Dipping in Alkali Solution
This is a technique of dipping the film in an alkali solution under appropriate conditions to saponify all the surface having reactivity with an alkali on the entire film surface. This method requires no special equipment and is preferred in view of cost. The alkali solution is preferably an aqueous sodium hydroxide solution. The concentration is preferably from 0.5 to 3 mol/L, more preferably from 1 to 2 mol/L. The liquid temperature of the alkali solution is preferably from 30 to 75° C., more preferably from 40 to 60° C.
The combination of the saponification conditions is preferably a combination of relatively mild conditions but may be selected according to the materials or construction of the film or the objective contact angle.
The film after dipping in an alkali solution is preferably well washed with water or dipped in a dilute acid to neutralize the alkali component and not to allow remaining of the alkali component in the film.
By applying the saponification treatment, the surface opposite the surface having the coating layer is hydrophilized. The polarizing plate protective film is used by bonding the hydrophilized surface of the transparent support to the polarizing film.
The hydrophilized surface is effective for improving the adhesive property to the adhesive layer comprising polyvinyl alcohol as the main component.
As for the saponification treatment, the contact angle for water on the transparent support surface opposite the surface having the coating layer is preferably lower in view of adhesive property to the polarizing film, but, on the other hand, in the dipping method, the surface having the coating layer as well as the inside of the layer are damaged simultaneously by an alkali and therefore, it is important to select minimum necessary reaction conditions. Particularly, in the case where the transparent support is triacetyl cellulose, the contact angle for water of the transparent support surface on the opposite side, when used as an index for the damage of each layer by an alkali, is preferably from 10 to 50°, more preferably from 30 to 50°, still more preferably from 40 to 50°. If the contact angle exceeds 50°, there arises a problem in the adhesive property to the polarizing film and this is not preferred, whereas if the contact angle is less than 10°, the film is too much damaged and the physical strength is disadvantageously impaired.
b. Method by Coating of Alkali Solution
In order to avoid the damage of each layer in the dipping method, an alkali solution coating method where an alkali solution is coated only on the surface opposite the surface having the coating layer under appropriate conditions and the coated solution is then heated, water-washed and dried, is preferably used. In this case, the “coating” means to contact an alkali solution or the like only with the surface to be saponified and includes spraying or contact with a belt or the like impregnated with the solution, other than coating. When such a method is employed, equipment and step for coating the alkali solution are separately required and therefore, this method is inferior to the dipping method of (1) in view of the cost. However, since the alkali solution comes into contact only with the surface to be saponified, a layer using a material weak to an alkali solution can be provided on the opposite surface. For example, a vapor-deposition film or a sol-gel film is subject to various effects such as corrosion, dissolution and separation by an alkali solution and is not preferably provided in the case of dipping method, but in this coating method, such a film is not contacted with the solution and therefore, can be used without problem.
The saponification methods (1) and (2) either can be performed after unrolling a rolled support and forming respective layers and therefore, the treatment may be added after the film production step and performed in a series of operations. Furthermore, by continuously performing also a step of laminating the film to a polarizing plate comprising a support unrolled similarly, a polarizing plate can be produced with higher efficiency than in the case of performing the same operations in the sheet-fed manner.
c. Method of Performing Saponification with Protection by Laminate Film
Similarly to (2) above, when the coating layer is insufficient in the resistance against an alkali solution, a method of, after a final layer is formed, laminating a laminate film on the surface where the final layer is formed, then dipping the stack in an alkali solution to hydrophilize only the triacetyl cellulose surface opposite the surface where the final layer is formed, and thereafter peeling off the laminate film, may be employed. Also in this method, a hydrophilizing treatment enough as a polarizing plate protective film can be applied only to the triacetyl cellulose film surface opposite the surface where the final layer is formed, without damage to the coating layer. As compared with the method (2), this method is advantageous in that a special apparatus for coating an alkali solution is not necessary, though the laminate film remains as a waste.
d. Method by Dipping in Alkali Solution After Formation up to Mid-Layer
In the case where the layers up to a lower layer have resistance against an alkali solution but a layer thereon is insufficient in the resistance against an alkali solution, a method of forming the layers up to the lower layer, then dipping the stack in an alkali solution to hydrophilize both surfaces, and thereafter forming the upper layer thereon, may be employed. The production process becomes cumbersome but this method is advantageous in that, for example, in a film comprising a hardcoat layer and a low refractive index layer formed of a fluorine-containing sol-gel film, when the layers have a hydrophilic group, the interlayer adhesion between the hardcoat layer and the low refractive index layer is enhanced.
e. Method of Forming Coating Layer on Previously Saponified Triacetyl Cellulose Film
After previously saponifying a triacetyl cellulose film, for example, by dipping it in an alkali solution, a coating layer may be formed on either one surface directly or through another layer. In the case of performing the saponification by dipping the film in an alkali solution, the interlayer adhesion to the triacetyl cellulose surface hydrophilized by the saponification is sometimes worsened. In such a case, the problem can be overcome by applying, after the saponification, a treatment such as corona discharge or glow discharge only to the surface where the coating layer is to be formed, thereby removing the hydrophilized surface, and then forming the coating layer. Also, when the coating layer has a hydrophilic group, good interlayer adhesion may be obtained.
The film of the present invention can be used as a protective film disposed on one side or both sides of a polarizing film, and the laminate can be used as a polarizing film.
While using the film of the present invention as one protective film, a normal cellulose acetate film may be used for the other protective film, but a cellulose acetate film produced by the above-described solution film-forming method and stretched in the width direction of a rolled film form at a stretch ratio of 10 to 100% is preferably used.
Furthermore, in the polarizing plate of the present invention, it is preferred that one surface is the optical film of the present invention and the other protective film is an optical compensation film having an optically anisotropic layer comprising a liquid crystalline compound.
The polarizing film includes an iodine-based polarizing film, a dye-based polarizing film using a dichroic dye, and a polyene-based polarizing film. The iodine-based polarizing film and the dye-based polarizing film are generally produced using a polyvinyl alcohol-based film.
The slow axis of the transparent support or cellulose acetate film of the optical film and the transmission axis of the polarizing film are arranged to run substantially in parallel.
The moisture permeability of the protective film is important for the productivity of the polarizing plate. The polarizing film and the protective film are laminated with an aqueous adhesive, and the solvent of this adhesive diffuses in the protective film and is thereby dried. As the moisture permeability of the protective film is higher, the drying rate and in turn the productivity are more elevated, but if the moisture permeability is excessively high, moisture enters into the polarizing film depending on the environment (at high humidity) where the liquid crystal display device is used, and the polarizing ability decreases.
The moisture permeability of the protective film is determined by the thickness, free volume or hydrophilicity/hydrophobicity of transparent support or polymer film (and polymerizable liquid crystal compound).
In the case of using the film of the present invention as a protective film of the polarizing plate, the moisture permeability is preferably from 100 to 1,000 g/m2·24 hrs, more preferably from 300 to 700 g/m2·24 hrs.
In the case of film production, the thickness of the transparent support can be adjusted by the lip flow rate and the line speed or by the stretching and compression. The moisture permeability varies depending on the main raw material used and therefore, can be adjusted to a preferred range by controlling the thickness.
In the case of film production, the free volume of the transparent support can be adjusted by the drying temperature and time.
Also in this case, the moisture permeability varies depending on the main raw material used and therefore, can be adjusted to a preferred range by controlling the free volume.
The hydrophilicity/hydrophobicity of the transparent support can be adjusted by an additive. The moisture permeability is elevated by adding a hydrophilic additive with the above-described free volume, and conversely, the moisture permeability can be lowered by adding a hydrophobic additive.
A polarizing plate having an optically compensating ability can be produced with high productivity at a low cost by independently controlling the moisture permeability.
The polarizing film may be a known polarizing film or a polarizing film cut out from a lengthy polarizing film with the absorption axis of the polarizing film being neither parallel nor perpendicular to the longitudinal direction. The lengthy polarizing film with the absorption axis of the polarizing film being neither parallel nor perpendicular to the longitudinal direction is produced by the following method.
This is a polarizing film obtained by stretching a continuously fed polymer film while holding its both edges with holding means and applying a tension and can be produced by a stretching method of stretching the film to from 1.1 to 20.0 times at least in the film width direction, moving the holding devices at both edges of the film to create a difference in the travelling speed of 3% or less in the longitudinal direction, and bending the film travelling direction in the state of the film being held at both edges such that the angle made by the film travelling direction at the outlet in the step of holding both edges of the film and the substantial stretching direction of the film is inclined at 20 to 70°. Particularly, a polarizing film produced with an inclination angle of 45° is preferred in view of productivity.
The stretching method of a polymer film is described in detail in JP-A-2002-86554 (paragraphs [0020] to [0030]).
It is also preferred that out of two protective films of a polarizer, the film other than the optical film of the present invention is an optical compensation film having an optical compensation layer comprising an optically anisotropic layer. The optical compensation film (phase difference film) can improve the viewing angle properties on a liquid crystal display screen.
The optical compensation film may be a known optical compensation film, but from the standpoint of enlarging the viewing angle, the optical compensation film described in JP-A-2001-100042 is preferred.
The optical film of the present invention is used for an image display device such as liquid crystal display (LCD), plasma display panel (PDP), electroluminescent display (ELD) and cathode ray tube display (CRT). The optical film of the present invention can be used on a known display such as plasma display panel (PDP) and cathode ray tube display (CRT).
The optical film or polarizing plate of the present invention can be advantageously used for an image display device such as liquid crystal display and is preferably used as the outermost surface layer of the display.
In general, the liquid crystal display device comprises a liquid crystal cell and two polarizing plates disposed on both sides thereof, and the liquid crystal cell carries a liquid crystal between two electrode substrates. In some cases, one optically anisotropic layer is disposed between the liquid crystal cell and one polarizing plate, or two optically anisotropic layers are disposed, that is, one between the liquid crystal cell and one polarizing plate, and another between the liquid crystal cell and another polarizing plate.
The liquid crystal cell is preferably in TN mode, STN mode, VA mode, OCB mode, IPS mode or ECB mode.
In the TN-mode liquid crystal cell, rod-like liquid crystalline molecules are oriented substantially in the horizontal alignment at the time of not applying a voltage and furthermore, twisted at an angle of 60 to 120°.
The TN-mode liquid crystal cell is most frequently utilized in a color TFT liquid crystal display device and is described in many publications.
In the STN-mode liquid crystal cell, rod-like liquid crystalline molecules are oriented substantially in the horizontal alignment at the time of not applying a voltage and furthermore, twisted at an angle of 150 to 300°.
The STN-mode liquid crystal cell is often utilized in a display device having a relatively small screen size and is described in many publications.
In the VA-mode liquid crystal cell, rod-like liquid crystalline molecules are oriented substantially in the vertical alignment at the time of not applying a voltage.
The VA-mode liquid crystal cell includes (1) a VA-mode liquid crystal cell in a narrow sense where rod-like liquid crystalline molecules are oriented substantially in the vertical alignment at the time of not applying a voltage and oriented substantially in the horizontal alignment at the time of applying a voltage (described in JP-A-2-176625); (2) an (MVA-mode) liquid crystal cell where the VA mode is modified to a multi-domain system for enlarging the viewing angle (described in SID97, Digest of Tech. Papers (preprints), 28, 845 (1997)); (3) an (n-ASM-mode) liquid crystal cell where rod-like liquid crystalline molecules are oriented substantially in the vertical alignment at the time of not applying a voltage and oriented in the twisted multi-domain alignment at the time of applying a voltage (described in preprints of Nippon Ekisho Toronkai (Liquid Crystal Forum of Japan), 58-59 (1998)); and (4) a SURVAIVAL-mode liquid crystal cell (reported in LCD International 98).
The OCB-mode liquid crystal cell is a liquid crystal cell of bend orientation mode where rod-like liquid crystalline molecules are oriented substantially in the reverse direction (symmetrically) between upper portion and lower portion of the liquid crystal cell, and this is disclosed in U.S. Pat. Nos. 4,583,825 and 5,410,422. Since rod-like liquid crystalline molecules are symmetrically oriented between upper portion and lower portion of the liquid crystal cell, the liquid crystal cell of bend orientation mode has an optically self-compensating ability. Accordingly, this liquid crystal mode is called an OCB (optically compensatory bend) liquid crystal mode. The liquid crystal display device of bend orientation mode is advantageous in that the response speed is fast.
The IPS-mode liquid crystal cell is a system of switching the nematic liquid crystal by applying a transverse electric field thereto, and this is described in detail in Proc. IDRC (Asia Display '95), pp. 577-580 and ibid., pp. 707-710.
In the ECB-mode liquid crystal cell, rod-like liquid crystalline molecules are oriented substantially in the horizontal alignment at the time of not applying a voltage. The ECB mode is one of liquid crystal display modes having a simplest structure and is described in detail, for example, in JP-A-5-203946.
The plasma display panel (PDP) is generally composed of a gas, a glass substrate, an electrode, an electrode lead material, a thick print material and a fluorescent material. As for the glass substrate, two sheets of front glass substrate and rear glass substrate are used. An electrode and an insulating layer are formed on the two glass substrates, and a fluorescent material layer is further formed on the rear glass substrate. The two glass substrates are assembled, and a gas is sealed therebetween.
The plasma display panel (PDP) is already available on the market. The plasma display panel is described in JP-A-5-205643 and JP-A-9-306366.
In some cases, a front panel is disposed on the front surface of the plasma display panel. The front panel preferably has sufficiently high strength for protecting the plasma display panel. The front panel may be disposed with spacing from the plasma display panel or may be laminated directly to the plasma display body. In an image display device like the plasma display panel, the optical filter can be laminated directly to the display surface. In the case where a front panel is provided in front of the display, the optical filter may be laminated to the front side (outer side) or back side (display side) of the front panel.
The optical film of the present invention can be applied to a touch panel and the like described, for example, in JP-A-5-127822 and JP-A-2002-48913.
The optical film of the present invention can be used as a substrate (substrate film) or protective film of an organic EL device or the like.
In the case of using the optical film of the present invention for an organic EL device or the like, the contents described, for example, in JP-A-11-335661, JP-A-11-335368, JP-A-2001-192651, JP-A-2001-192652, JP-A-2001-192653, JP-A-2001-335776, JP-A-2001-247859, JP-A-2001-181616, JP-A-2001-181617, JP-A-2002-181816, JP-A-2002-181617 and JP-A-2002-056976 may be applied. Furthermore, the contents described in JP-A-2001-148291, JP-A-2001-221916 and JP-A-2001-231443 are preferably used in combination.
The present invention is described below by referring to Examples, but the present invention is not limited thereto.
The average particle diameter of the organic resin particle was measured as follows.
The 50% volume diameter (median diameter) obtained by a laser diffraction/scattering particle size distribution measuring apparatus [Master Sizer 2000 (trade name), manufactured by Malvern Instruments Ltd.] was used as the average particle diameter.
The layer thickness of the shell was measured as follows.
An epoxy resin for embedding, the particle of the present invention and a curing agent were charged into a embedding board and thoroughly mixed, and the mixture was cured for one night in an oven at a temperature of 60° C. The cured product was sliced by a microtome [ULTRACUT N (trade name, manufactured by Reichert-Nissen], and the slice of the particle was photographed by a transmission electron microscope (TEM). The actual layer thickness of the sell was measured on the TEM photograph.
The refractive index can be determined by the following procedure of (1) to (3).
(1) A particle is placed on a slide glass and after adding a liquid organic compound or mixed organic compound shown in Table 2 (hereinafter referred to as a “compound”), sandwiched by a cover glass.
(2) The particle is observed using an optical microscope (transmitting) at 25° C. and the kind of the compound which makes the particle least visible is selected.
(3) The numerical value (Table 2) corresponding the compound which makes the particle least visible is used as the refractive index.
Incidentally, when a mixed organic compound is used, the refractive index can be determined by calculation on the assumption that there is additivity of the mixing ratio. For example, when toluene and nitrobenzene are mixed at 1:2, the refractive index becomes (1.496×1/3)+(1.550×2/3)=1.532 when calculated by referring to the numerical values shown in Table 2.
In a 2-liter reaction flask equipped with a stirrer, a reflux condenser and a thermometer, 80.0 g of melamine, 154.4 g of 37% formalin, 34.0 g of an aqueous silica sol [SNOWTEX O-40 (trade name), produced by Nissan Chemicals Industries, Ltd., SiO2 concentration: 40.7 mass %, pH: 2.4, average particle diameter: 23.0 nm], 1.0 g of sodium sulfate and 683 g of water were charged, and the pH was adjusted to 8.5 with 25% aqueous ammonia. Thereafter, the temperature was elevated while stirring the mixture and kept at 70° C. to allow the reaction to proceed for 30 minutes, whereby an aqueous solution of the initial condensate of melamine resin was prepared. The molecular weight of the melamine resin at this time was measured by the GPC method (in terms of polystyrene) and found to be 290. Subsequently, while keeping the temperature at 70° C., an aqueous 10 mass % paratoluenesulfonic acid monohydrate solution was added to the obtained aqueous solution of the initial condensate to adjust the pH to 5.1. After about 5 minutes, the reaction system became white turbid and the cured melamine resin particle was precipitated. The temperature was then elevated to 90° C. and the curing reaction was continued for 3 hours. After cooling, the pH of the obtained reaction solution was adjusted to 7.5 by using an aqueous 5 mass % sodium hydroxide solution, and the melamine resin particle powder separated by filtration was heat-treated at 150° C. for 3 hours in an atmosphere having an oxygen concentration of 8% under nitrogen purging and further ground in a pin-disc mill to obtain white Amino Resin Particle 1 (refractive index: 1.65). The obtained particles were measured by a laser diffraction/scattering particle size distribution measuring apparatus [Master Sizer 2000 (trade name), manufactured by Malvern Instruments Ltd.], as a result, the average particle diameter was 2.0 μm and the CV value was 5.8%. When the cured resin particles were as-is observed by a scanning electron microscope (SEM), only spherical particles were observed. Also, when the spherical particle in a sliced state was observed by the transmission electron microscope-energy dispersive X-ray analysis (TEM-EDX), it was confirmed that the particle comprises a melamine resin-silica composite layer where the core is the melamine resin and the shell is formed of a colloidal silica having a particle diameter of 23 nm and being densely filled in the particle surface and that the layer thickness of the sell is 90 nm.
In a 2-liter reaction flask equipped with a stirrer, a reflux condenser and a thermometer, 80.0 g of melamine, 154.4 g of 37% formalin, 34.0 g of an aqueous silica sol [SNOWTEX O-40 (trade name), produced by Nissan Chemicals Industries, Ltd., SiO2 concentration: 40.7 mass %, pH: 2.4, average particle diameter: 23.0 nm], 1.0 g of sodium sulfate and 683 g of water were charged, and the pH was adjusted to 8.5 with 25% aqueous ammonia. Thereafter, the temperature was elevated while stirring the mixture and kept at 70° C. to allow the reaction to proceed for 30 minutes, whereby an aqueous solution of the initial condensate of melamine resin was prepared. The molecular weight of the melamine resin at this time was measured by the GPC method (in terms of polystyrene) and found to be 290. Subsequently, while keeping the temperature at 70° C., an aqueous 10 mass % paratoluenesulfonic acid monohydrate solution was added to the obtained aqueous solution of the initial condensate to adjust the pH to 5.1. After about 5 minutes, the reaction system became white turbid and cured melamine resin particles were precipitated. The temperature was then elevated to 90° C. and the curing reaction was continued for 3 hours. Thereafter, the reaction system was cooled, and 50 g of melamine resin particles recovered by precipitation separation, 450 g of water and 0.5 g of ammonium sulfamate were charged into a 2-liter autoclave. After purging with nitrogen, the temperature was elevated to 170° C. and the particles were heat- and pressure-treated for 3 hours. Following this treatment, the particles were separated by filtration, washed with pure water several times, then heat-treated at 150° C. for 3 hours in an atmosphere having an oxygen concentration of 8% under nitrogen purging, and further ground in a pin-disc mill to obtain white Amino Resin Particle 2 (refractive index: 1.64). The obtained particles were measured by a laser diffraction/scattering particle size distribution measuring apparatus [Master Sizer 2000 (trade name), manufactured by Malvern Instruments Ltd.], as a result, the average particle diameter was 2.0 μm and the CV value was 6.1%. When the cured resin particles were as-is observed by a scanning electron microscope (SEM), only spherical particles were observed. Also, when the spherical particle in a sliced state was observed by the transmission electron microscope-energy dispersive X-ray analysis (TEM-EDX), it was confirmed that the particle comprises a melamine resin-silica composite layer where the core is the melamine resin and the shell is formed of a colloidal silica having a particle diameter of 23 nm and being densely filled in the particle surface and that the layer thickness of the sell is 90 nm.
In a 2-liter reaction flask equipped with a stirrer, a reflux condenser and a thermometer, 80.0 g of melamine, 154.4 g of 37% formalin, 34.0 g of an aqueous silica sol [SNOWTEX O-40 (trade name), produced by Nissan Chemicals Industries, Ltd., SiO2 concentration: 40.7 mass %, pH: 2.4, average particle diameter: 23.0 nm], 1.0 g of sodium sulfate and 683 g of water were charged, and the pH was adjusted to 8.5 with 25% aqueous ammonia. Thereafter, the temperature was elevated while stirring the mixture and kept at 70° C. to allow the reaction to proceed for 30 minutes, whereby an aqueous solution of the initial condensate of melamine resin was prepared. The molecular weight of the melamine resin at this time was measured by the GPC method (in terms of polystyrene) and found to be 290. Subsequently, while keeping the temperature at 70° C., an aqueous 10 mass % paratoluenesulfonic acid monohydrate solution was added to the obtained aqueous solution of the initial condensate to adjust the pH to 5.1. After about 5 minutes, the reaction system became white turbid and the cured melamine resin particle was precipitated. The temperature was then elevated to 90° C. and the curing reaction was continued for 3 hours. Thereafter, the reaction system was cooled, the obtained reaction solution was filtered and dried, and the particle solid powder was recovered and ground in a pin-disc mill to obtain white cured amino resin particles (refractive index: 1.63). The obtained particles were measured by a laser diffraction/scattering particle size distribution measuring apparatus [Master Sizer 2000 (trade name), manufactured by Malvern Instruments Ltd.], as a result, the average particle diameter was 2.0 μm. When the cured resin particles were as-is observed by a scanning electron microscope (SEM), only spherical particles were observed. Also, when the spherical particle in a sliced state was observed by the transmission electron microscope-energy dispersive X-ray analysis (TEM-EDX), it was confirmed that the particle comprises a melamine resin-silica composite layer where the core is the melamine resin and the shell is formed of a colloidal silica having a particle diameter of 23 nm and being densely filled in the particle surface and that the layer thickness of the sell is 90 nm.
The components shown below were charged into a mixing tank and after stirring, the resulting solution was filtered through a polypropylene-made filter having a pore size of 30 μm to prepare the coating solution.
The components above are as follows.
Produced by Nippon Kayaku Co., Ltd., refractive index: 1.51
Photopolymerization initiator (produced by Ciba Specialty Chemicals Corp.)
Polyether-modified silicone (produced by Toray Dow Corning)
In a reaction vessel equipped with a stirrer and a reflux condenser, 120 parts of methyl ethyl ketone, 100 parts of acryloxypropyltrimethoxysilane (KBM-5103, produced by Shin-Etsu Chemical Co., Ltd.) and 3 parts of diisopropoxyaluminum ethyl acetate were added and mixed and after adding 30 parts of ion-exchanged water, the reaction was allowed to proceed at 60° C. for 4 hours. The reaction solution was then cooled to room temperature to obtain Sol Solution a.
The mass average molecular weight was 1,800 and out of the oligomer or higher components, the proportion of the components having a molecular weight of 1,000 to 20,000 was 100%. Also, the gas chromatography analysis revealed that the raw material acryloxypropyltrimethoxysilane was not remaining at all.
30 Parts of acryloyloxypropyltrimethoxysilane (produced by Shin-Etsu Chemical Co., Ltd.) and 1.5 parts of diisopropoxyaluminum ethyl acetate were added and mixed to 500 parts of a hollow silica fine particle sol (isopropyl alcohol silica sol, average particle diameter: 60 nm, thickness of shell: 10 nm, silica concentration: 20 mass %, refractive index of silica particle: 1.31, prepared according to Preparation Example 4 of JP-A-2002-79616 by changing the size), and 9 parts of ion-exchanged water was added thereto. After allowing the reaction to proceed at 60° C. for 8 hours, the reaction solution was cooled to room temperature, and 1.8 parts of acetyl acetone was added. While adding cyclohexanone to 500 g of the resulting liquid dispersion to keep almost constant the silica content, solvent replacement by reduced-pressure distillation was performed under a pressure of 20 kPa. Foreign matters were not generated in the liquid dispersion and when the solid content concentration was adjusted to 20 mass % with cyclohexanone, the viscosity was 5 mPa·s at 25° C. The amount of isopropyl alcohol remaining in the obtained Hollow Silica Fine Particle Sol Liquid Dispersion a was analyzed by gas chromatography and found to be 1.5%.
Dimethyloctadecyl-3-trimethoxy•silylpropylammonium chloride (XS70-241, produced by Toshiba Silicone) was added to a hollow silica fine particle sol (isopropyl alcohol silica sol, average particle diameter: 60 nm, thickness of shell: 10 nm, silica concentration: 20 mass %, refractive index of silica particle: 1.31, prepared according to Preparation Example 4 of JP-A-2002-79616 by changing the size) in an amount of 5 mass % per 100 parts by mass of silica, and the mixture was heat-treated at 50° C. for 1 hour to obtain an isopropyl alcohol liquid dispersion containing 20 mass % of a surface-treated silica fine particle having voids. While adding methyl isobutyl ketone to this liquid dispersion to keep almost constant the silica content, solvent replacement by reduced-pressure distillation was performed under a pressure of 20 kPa. Foreign matters were not generated in the liquid dispersion. The solid content concentration was then adjusted to 20 mass % with methyl isobutyl ketone. The amount of isopropyl alcohol remaining in the obtained Hollow Silica Fine Particle Sol Liquid Dispersion b was analyzed by gas chromatography and found to be 1.5%.
The components shown below were charged into a mixing tank and after stirring, the resulting solution was filtered through a polypropylene-made filter having a pore size of 3 μm to prepare the coating solution.
The components above are as follows.
The fluorine-containing and silicone-containing heat-curable polymer described in Example 1 of JP-A-11-189621
Curing agent (produced by Nihon Cytec Industries Inc.)
Curing catalyst (produced by Nihon Cytec Industries Inc.)
Colloidal silica liquid dispersion (produced by Nissan Chemicals Industries, Ltd., average particle diameter: 45 nm, solid content concentration: 30%)
Photopolymerization initiator (produced by Ciba Specialty Chemicals Corp.)
Antistatic agent (a quaternary ammonium compound, produced by Mitsui Bussan Plastics Co., Ltd.)
Pentaerythritol triacrylate (produced by Nippon Kayaku Co., Ltd., refractive index: 1.51)
Using the slot die coater shown in
After coating various hardcoat layers, Coating Solutions LL-1 to LL-3 for Low Refractive Index Layer corresponding to Table 3 each was wet-coated thereon by a slot die coater shown in
The internal haze was measured by NDH2000 (Nippon Denshoku Industries Co., Ltd.). The measuring method is as follows.
After adding several silicone oil drops on the front and back surfaces of the optical film, the film was sandwiched front and back by two 1 mm-thick glass plates (Microslide Glass No. S9111, produced by Matsunami K. K.), the haze was measured according to JIS-K7136 in a state of two glass plates being in complete contact with the optical film obtained, and the value obtained by subtracting, from this haze value, the haze separately measured by interposing only the silicone oil between two glass plates was calculated as the internal haze.
The entire beam transmittance is measured by NDH2000 (Nippon Denshoku Industries Co., Ltd.).
The Ra (arithmetic average roughness) is measured according to JIS-B0601 by a two-dimensional roughness gauge, Model SJ-400, manufactured by Mitsutoyo.
The percentage changes in the internal haze and in the entire beam transmittance after the optical film was left standing in an environment at a temperature of 80° C. and a relative humidity of 90% for 500 hours were measured.
Percentage change (%)={[(internal haze before test)−(internal haze after test)]/(internal haze before test)}×100
In the measurement of integrated reflectance, the transparent support surface of the film was roughened with sand paper and then treated with black ink to eliminate the back surface reflection and in this state, the integrated reflectance was measured in the wavelength region of 380 to 780 nm by loading an adapter, “ILV-471”, on a spectrophotometer, “V-550” [manufactured by JASCO Corp.]. The average integrated reflectance at 450 to 650 nm was calculated and used for the evaluation of antireflective property.
In a four-neck flask, 75 parts of melamine, 75 parts of benzoguanamine, 238 parts of formalin in a concentration of 37% and 1.07 parts of an aqueous sodium carbonate solution in a concentration of 10% were charged to obtain a mixture. While stirring the mixture, polymerization was allowed to proceed by elevating the temperature to 85° C. to obtain an initial condensate having a degree of water compatibility of 250%. Separately, 6.0 parts of a nonionic surfactant, EMULGEN 430 (produced by Kao Corp., polyoxyethylene oleyl ether), was dissolved in 2,455 parts of water, and the temperature of this aqueous surfactant solution was elevated to 50° C., followed by stirring. The initial condensate obtained above was charged into the aqueous surfactant solution under stirring to obtain an emulsion of the initial condensate. After adding 90 parts of an aqueous 5% dodecylbenzenesulfonic acid solution thereto, the emulsion was condensed and cured by keeping it at a temperature of 50 to 60° C. for 3 hours to obtain an emulsion of the cured resin. This emulsion was charged into 3,000 parts of cold water and thereby rapidly cooled. Subsequently, the cured resin was precipitated and separated from this emulsion, and using an ultrasonic disperser, the obtained paste was dispersed in an aqueous solution obtained by dissolving 7.5 parts of EMULGEN 430 and 4.5 parts of dodecylbenzenesulfonic acid in 2,000 parts of water. The emulsion obtained after dispersion was again condensed and cured by gradually elevating the temperature to 90° C. and after holding for 1 hour, rapidly cooled. The cured resin was precipitated and separated from this emulsion to obtain cured spherical fine particles of the amino resin of melamine/benzoguanamine/formaldehyde.
Subsequently, 50 g of cured spherical fine particles of the amino resin, 450 g of water and 0.5 g of ammonium sulfamate were charged into a 2-liter autoclave and after purging with nitrogen, the mixture was heat- and pressure-treated for 3 hours by elevating the temperature to 170° C. After this treatment, the particles were separated by filtration, washed with pure water several times, then heat-treated and thereby dried at 160° C. for 4 hours, and further ground to obtain white Amino Resin Particle 4. As for the particle size distribution of Amino Resin Particle 4, the particles were measured by a laser diffraction/scattering particle size distribution measuring apparatus [Master Sizer 2000 (trade name), manufactured by Malvern Instruments Ltd.], as a result, the average particle diameter was 3.5 μm and the CV value was 3.2%. The NMR area ratio C(II)/C(I) of Amino Resin Particle 4 was 3.9, the compressive modulus at 10% deformation was 1,050 kg/mm2, and the refractive index at 25° C. was 1.61.
White Amino Resin Particle 5 was obtained by the same operation except that in the synthesis method of Amino Resin Particle 4, 75 parts of melamine and 75 parts of benzoguanamine were changed to 150 parts of melamine. As for the particle size distribution of Amino Resin Particle 5, the particles were measured by a laser diffraction/scattering particle size distribution measuring apparatus [Master Sizer 2000 (trade name), manufactured by Malvern Instruments Ltd.], as a result, the average particle diameter was 2.2 μm and the CV value was 3.9%. The NMR area ratio C(II)/C(I) of Amino Resin Particle 5 was 4.1, the compressive modulus at 10% deformation was 1,590 kg/mm2, and the refractive index at 25° C. was 1.63.
White Amino Resin Particle 6 was obtained by the same operation except that in the synthesis method of Amino Resin Particle 4, the temperature at the heat treatment (drying) after separation and washing of particles was changed from 160° C. to 90° C. As for the particle size distribution of Amino Resin Particle 6, the particles were measured by a laser diffraction/scattering particle size distribution measuring apparatus [Master Sizer 2000 (trade name), manufactured by Malvern Instruments Ltd.], as a result, the average particle diameter was 3.53 μm and the CV value was 3.8%. The NMR area ratio C(II)/C(I) of Amino Resin Particle 6 was 1.2, the compressive modulus at 10% deformation was 950 kg/mm2, and the refractive index at 25° C. was 1.55.
In a vessel containing a solution comprising 7.8 g of mercaptopropyltrimethoxysilane and 0.2 g of dibutyltin laurate, 20.66 g of isophorone diisocyanate was added dropwise under the conditions of 50° C. and 1 hour in dry air, and the resulting solution was stirred under the conditions of 60° C. and 3 hours. Furthermore, pentaerythritol and 71.4 g of triacrylate were added dropwise thereto under the conditions of 30° C. and 1 hour, and the resulting solution was stirred under the conditions of 60° C. and 3 hours to obtain a reaction solution. The amount of residual isocyanate in the product, that is, the reactive alkoxysilane in the reaction solution was measured by FT-IR and found to be 0.1 mass % or less, revealing that the nuclear reaction was almost quantitatively performed. Also, it was confirmed that a thiourethane bond, a urethane bond, an alkoxysilyl group and a reactive unsaturated bond are contained in the molecule.
Subsequently, 200 g of MEK and 60 g of Amino Resin Particle 5 were charged into a vessel with a stirrer and stirred, and the resulting solution was mixed with 25 g of the reactive alkoxysilane obtained above, 0.3 g of distilled water and 0.03 g of p-hydroxyphenyl monomethyl ether and then stirred under heating at 65° C. After 5 hours, 8 g of methyl ortho-formate was added, and the reaction system was heated for 1 hour. Furthermore, 6.1 g of Irgacure 907 (produced by Ciba Specialty Chemical Corp.) as a photopolymerization initiator and 1.7 g of MIBK were added, and the reactive unsaturated group coated on the surface was crosslinked by irradiating light from a mercury lamp to obtain white Amino Particle 7. As for the particle size distribution of Amino Resin Particle 7, the particles were measured by a laser diffraction/scattering particle size distribution measuring apparatus [Master Sizer 2000 (trade name), manufactured by Malvern Instruments Ltd.], as a result, the average particle diameter was 2.3 μm and the CV value was 3.8%. Also, when this spherical particle in a sliced state was observed by the transmission electron microscope-energy dispersive X-ray analysis (TEM-EDX), it was confirmed that the core is the melamine resin, the shell is formed of a colloidal silica having a particle diameter of 23 nm and being densely filled in the particle surface to a thickness of 90 nm, and a cured organic film is further formed thereon to a thickness of 100 nm. The NMR area ratio C(II)/C(I) of Amino Resin Particle 7 was 4.1, the compressive modulus at 10% deformation was 1,590 kg/mm2, and the refractive index at 25° C. was 1.63.
The components shown below were charged into a mixing tank and after stirring, the resulting solution was filtered through a polypropylene-made filter having a pore size of 30 μm to prepare the coating solution.
The components above are as follows.
Produced by Nippon Kayaku Co., Ltd., refractive index: 1.51
Pentaerythritol triacrylate (produced by Nippon Kayaku Co., Ltd., refractive index: 1.51)
Photopolymerization initiator (produced by Ciba Specialty Chemicals Corp.)
Photopolymerization initiator (produced by Ciba Specialty Chemicals Corp.)
Polyether-modified silicone (produced by Toray Dow Corning)
The hardcoat layer was provided by coating in the same manner as in Example 1, and Optical Films (AF-8 to AF-11) each having a 6 μm-thick hardcoat layer were produced.
Also, the heat and humidity test of the obtained optical film was performed in the same manner as in Example 1.
A polarizing film was produced by adsorbing iodine to a stretched polyvinyl alcohol film. Example Sample AF-5 was saponified and laminated to one side of the polarizing film by using a polyvinyl alcohol-based adhesive, such that the transparent substrate film (cellulose triacetate) of Example Sample AF-5 came to the polarizing film side. Also, Optical Compensation Film (KH-01) shown below was laminated to the opposite side of the polarizing film by using a polyvinyl alcohol-based adhesive, such that the cellulose acetate film came to the polarizing film side. The transmission axis of the polarizing film and the slow axis of KH-01 were arranged to run in parallel. In this way, Polarizing Plate (HKH-01) with a light-diffusing layer was produced.
The cellulose acetate solution was prepared by charging the following composition into a mixing tank and stirring it under heating to dissolve respective components.
In a separate mixing tank, 25 parts by mass of the retardation raising agent shown below as a wavelength-dispersion controlling agent, 80 parts by mass of methylene chloride and 20 parts by mass of methanol were charged and stirred under heating to prepare a retardation raising agent solution. 7 Parts by mass of the retardation raising agent solution was mixed with 493 parts by mass of the cellulose acetate solution, and the mixed solution was thoroughly stirred to prepare a dope. The amount of the retardation raising agent added was 1.5 parts by mass per 100 parts by mass of cellulose acetate.
The dope obtained was cast using a band casting machine. After the film surface temperature on the band reached 40° C., the film was dried for 1 minute, then peeled off and further dried with dry air at 140° C. to produce a cellulose acetate film (thickness: 90 μm) having a residual solvent amount of 0.3 mass %. The optical properties of the produced Cellulose Acetate Film (CAF-01) were measured, as a result, the Re retardation value was 5 nm and the Rth retardation value was 80 nm. Incidentally, in the measurement of optical properties, the Re retardation value and Rth retardation value at a wavelength of 550 nm were measured using an ellipsometer (M150, manufactured by JASCO Corp.).
The produced cellulose acetate film was coated with 5 ml/m2 of 1.5 N potassium hydroxide (water/IPA/PG=14/86/15 vol %), then kept at 60° C. for about 10 seconds and after water-washing the potassium hydroxide remaining on the film surface, dried. The surface energy of this cellulose acetate film was measured by the contact angle method and found to be 63 mN/m. On this cellulose acetate film, a coating solution having the following composition was coated by a #16 wire bar to have a coverage of 28 ml/m2, and dried with warm air at 60° C. for 60 seconds and further with warm air at 90° C. for 150 seconds. Subsequently, the film formed was subjected to rubbing in the direction parallel to the longitudinal direction of the cellulose acetate film.
On the orientation film, a coating solution obtained by dissolving 41.01 g of the discotic (liquid crystalline) compound shown below, 4.06 g of ethylene oxide-modified trimethylolpropane triacrylate (V#360, produced by Osaka Organic Chemical Industry Ltd.), 0.90 g of cellulose acetate butyrate (CAB551-0.2, produced by Eastman Chemical), 0.23 g of cellulose acetate butyrate (CAB531-1, produced by Eastman Chemical), 1.35 g of a photopolymerization initiator (Irgacure 907, produced by Ciba Geigy) and 0.45 g of a sensitizer (Kayacure DETX, produced by Nippon Kayaku Co., Ltd.) in 102 g of methyl ethyl ketone was coated by a #3.6 wire bar. This coating was heated in a constant-temperature zone at 130° C. for 2 minutes to align the discotic compound, then irradiated with UV for 1 minute by using a high-pressure mercury lamp of 120 W/cm in an atmosphere of 60° C. to polymerize the discotic compound, and then allowed to cool to room temperature, thereby forming an optically anisotropic layer. In this way, Optical Compensation Film (KH-01) was produced. The Re retardation value of the optically anisotropic layer measured at a wavelength of 550 nm was 43 nm. Also, the angle (tilt angle) between the discotic plane and the first transparent support plane was 42° on average.
A pair of polarizing plates provided in a liquid crystal display device (6E-A3, manufactured by Sharp Corp.) using a TN-mode liquid crystal cell were removed, and Polarizing Plate (HKH-01) was instead laminated on the viewer side through a pressure-sensitive adhesive such that KH-01 came to the liquid cell side. On the backlight side, the following Polarizing Plate (HKH-S1) was laminated. HKH-S1 was prepared by laminating Optical Compensation Film (KH-01) to one side of the polarizing film by using a polyvinyl alcohol-based adhesive such that the cellulose acetate film came to the polarizing film side, and laminating a cellulose acetate film (FUJI-TAC TD80UF, produced by Fuji Photo Film Co., Ltd.) to another side. The transmission axis of the polarizing film and the slow axis of KH-01 were arranged to run in parallel. In this way, Polarizing Plate (HKH-S1) on the backlight side was produced. The transmission axis of the viewer-side polarizing plate and the transmission axis of the backlight-side polarizing plate were arranged to be in O mode. The viewing angle of the liquid crystal display device produced was measured in 8 steps from black display (L1) to white display (L8) by using a measuring apparatus (EZ-Contrast 160D, manufactured by ELDIM). The results are shown in Table 6.
Also, Polarizing Plate (HKH-H1) was produced by laminating a commercially available cellulose triacetate film (FUJI-TAC TD80UF, produced by Fuji Photo Film Co., Ltd.) in place of Optical Compensation Film (KH-01) of Polarizing Plate (HKH-01) with a light-diffusing layer, and measured in the same manner as in the evaluation of Polarizing Plate (HKH-01) with a light-diffusing layer. The results are shown in Table 6.
Even when the support of Optical Compensation Film (KH-01) of Polarizing Plate (HKH-01) with a light-diffusing layer was changed to the film described in JP-A-2006-030937, the same effects were obtained.
The optical film of the present invention enables an image display device assured of [1] more enhanced display quality, [2] low cost, [3] reduced fluctuation of light scattering property at the production, and [4] small change in light scattering property under high-temperature high-humidity conditions (specifically, 80° C. and 90% RH). The image display device using the optical film of the present invention can be enlarged in the viewing angle and be almost free from contrast reduction due to change in the viewing angle or from occurrence of tone or black-and-white reversal, color hue change and the like.
The entire disclosure of each and every foreign patent application from which the benefit of foreign priority has been claimed in the present application is incorporated herein by reference, as if fully set forth.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2006-244500 | Sep 2006 | JP | national |
| 2006-311537 | Nov 2006 | JP | national |
