A polarization light splitting film having a light receiving side and a light transmitting side. The polarization light splitting film includes an optical rotation selection layer at the light receiving side for reflecting one of right and left circularly polarized components of a light beam that is incident on the light receiving side and for transmitting the other one of the right and left circular polarization components of the light beam, and a quarter-wave layer laminated over the optical rotation selection layer at the light transmitting side.
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0. 13. A polarization light splitting film having a light receiving side and a light transmitting side, the polarization light splitting film comprising:
an optical rotation selection layer at the light receiving side for reflecting one of right and left circularly polarized components of a light beam that is incident on the light receiving side and for transmitting the other one of the right and left circularly polarized components of the light beam;
a quarter-wave layer laminated over the optical rotation selection layer at the light transmitting side and for emitting linearly polarized light;
a linear polarizing layer laminated over the quarter-wave layer at the light transmitting side and having a polarization axis which substantially matches a polarization axis of the linearly polarized light emitted from the quarter-wave layer; and
a diffusion layer disposed under the optical rotation selection layer at the light receiving side, the diffusion layer including at least two types of diffusion agents, each agent having a different average particle diameter within the range of 1 μm to 50 μm.
0. 1. A polarization light splitting film having a light receiving side and a light transmitting side, the polarization light splitting film comprising:
an optical rotation selection layer at the light receiving side for reflecting one of right and left circularly polarized components of a light beam that is incident on the light receiving side and for transmitting the other one of the right and left circularly polarized components of the light beam;
a quarter-wave layer laminated over the optical rotation selection layer at the light transmitting side and for emitting linearly polarized light;
a linear polarizing layer laminated over the quarter-wave layer at the light transmitting side and having a polarizing axis which substantially matches a polarization axis of the linearly polarized light emitted from the quarter-wave layer; and
a diffusion layer disposed under the optical rotation selection layer at the light receiving side, the diffusion layer including a diffusion agent having an average particle diameter of 1 to 50 μm.
0. 2. The polarization light splitting film according to
0. 3. The polarization light splitting film according to
0. 4. The polarization light splitting film according to
0. 5. The polarization light splitting film according to
0. 6. The polarization light splitting film according to
0. 7. The polarization light splitting film according to
0. 8. The polarization light splitting film according to
0. 9. The polarization light splitting film according to
0. 10. The polarization light splitting film according to
0. 11. The polarization light splitting film according to
0. 12. The polarization light splitting film according to
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Here, p is the helical pitch, and nAV is an average refractive index in a plane perpendicular to the helical axis. The wavelength bandwidth Δλ of the reflected light is given in the following Equation (2).
Δλ=Δn·p (2)
where Δn=n∥−n⊥, n∥ is the maximum refractive index in a plane perpendicular to the helical axis, and n⊥ is the maximum refractive index in a plane parallel to the helical axis. Also, it is known that the wavelength λφ of the selectively scattered light, originating from the light obliquely incident on the liquid crystal layer with respect to the helical axis of the planar structure, is shifted from λ0 toward the shorter wavelength.
Using the above-mentioned characteristics, it is possible to use only light having a certain wavelength. Alternatively, the helical pitch p and the refractive index difference Δn of the cholesteric liquid crystal may be adjusted such that the wavelength bandwidth Δλ of the reflected light covers the entire range of visible light, making it possible to use white light.
As such a cholesteric liquid crystal, it is desirable to use chiral nematic liquid crystal compounds in which an optically active substance, such as a 2-methylbutyl group, 2-methylbutoxy group, or 4-methylhexyl group, is attached to the end group of a nematic liquid crystal compound, such as a schiff base, azo-system, ester-system, or biphenyl-system.
Also, cholesteric liquid crystal polymers are among the preferable materials for the cholesteric liquid crystal of the present invention. This is because the cholesteric liquid crystal polymer is in its solid phase at a room temperature, and its chiral characteristics are easily maintained. In general, to form a liquid crystal polymer, a mesogen group of a liquid crystal phase is introduced in the main chain and/or the side chain. The cholesteric liquid crystal polymer can also be obtained by introducing a cholesteril group in the side chain, for example. In this case, the cholesteril group can be introduced to the side chain of a main chain polymer of polysiloxane or a vinyl polymer, such as an ethyiene-vinyl acetate copolymer, through a spacer (molecular) providing an appropriate distance. Alteratively, a vinyl monomer having a cholesteril group may be polymerized to produce the cholesteric liquid crystal polymer.
The optical rotation selection layer of the present invention may have a single layered structure of a cholesteric liquid crystal layer or a multi-layer structure in which an optical rotation selection layer is coated on a base member (substrate). In the polarization light splitting film 10 shown in
These multi-layer structures are useful when the optical rotation selection layer is too thin to be handled with ease or when there is difficulty in laminating the optical rotation selection layer together with the quarter-wave layer. In addition, with the multi-layer of the cholesteric liquid crystal layer and the substrate of
In the case of the single layered structure of
A resin film can be used as the substrate 3. The desirable properties of such a resin film include superior transparency, dimensional stability, and coating ability. In particular, films made from polyethyleneterephtalate, polyethylenenaphtalate, polycarbonate, polyethersulfone, and/or acrylic resin are preferable.
The quarter-wave layer 2 may be formed using various methods: laminating multiple layers having different refractive indices, providing a specific orientation in liquid crystal, or orienting molecules by stretching in a predetermined direction a resin film made of, for example, polyesters such as polyethyleneterephtalate, polyethersulfone, polycarbonate, polysulfone, polyetheretherketone, or polyetherketone. Typically, the thickness of the quarter-wave layer 2 is set to approximately 8 to 100 μm.
As shown in
Polarization light splitting film 10 shown in
The diffusion layer 5 may be formed by dispersing diffusive agents in a light transmitting resin, utilizing the optical scattering effect due to the difference in refractive index between the diffusion agent and the light transmitting resin, or by forming an uneven surface on a light transmitting resin. Examples of the diffusion agent are beads, fillers and hollow beads with the main component being an acrylic resin, polystyrene, polyethylene, ureaformaldehyde resin, urethane resin, organic silicon resin, calcium carbonate, titanium oxide, or silica. It is desirable that the average particle diameter of the diffusion agent be 1 to 50 μm to facilitate handling. Also, two or more types of agent, with different particle diameters, may be used. Examples of the light transmitting resin are a polyester system resin, acrylic system resin, polystyrene system resin, polyvinylchloride system resin, polyvinylidenechloride system resin, polyethylene system resin, polypropylene system resin, polyurethane system resin, polyamide system resin, polyvinylactate system resin, polyvinylalcohol system resin, epoxy system resin, cellulose system resin, silicon system resin, polymimide system resin, polysulfone system resin, and polyarylate system resin.
Polarization light splitting film 10 in
Polarization light splitting film 10 shown in
The above-mentioned prism layer and lens layer can be formed by various methods: a thermal press method in which the uneven shape is molded on the specimen's surface by pressing a high-temperature molding form on a resin film in a thermoplastic state; a simultaneous extrusion-embossing method in which, when a resin is formed into a film shape by melting-extrusion at a high temperature, an uneven shape is concurrently formed on the surface by an embossing roll; or a 2P (Photo Polymer) method in which an ionizing radiation-setting resin is molded on a resin film by a mold form and then cured. The resultant film with the uneven surface is adhered to the optical rotation selection layer with an adhesive or is used as the substrate.
The resin film that can be used in the above-mentioned thermal press method and simultaneous extrusion-embossing method includes, for example, acrylic resins, polycarbonate resins, polyester resins such as polyethyleneterephtalate, polystyrene resin, and vinylchloride resin.
Examples of the ionizing radiation-setting resin that can be used in the above-mentioned 2P method include, for example, known ultraviolet-setting resins and electron beam setting resins, represented by compounds made from a prepolymer and/or a monomer that has in its molecules a functional polymerization group, such as a (meta)-acryloyl group (here and in the following description, “(meta)” is used to represent both with and without “meta”, i.e., acryloyl group and meta-acryloyl group), a (meta)acryloyloxy group, epoxy group, or a mercapto group.
For example, the main component of such a compound is a prepolymer, such as urethane(meta)acrylate, epoxy(meta) acryalte, or silicon(meta)acrylate, or a multifunctional monomer, such as trimethylolpropanetri(meta)acrylate, or dipentaerythritolhexa(meta)acrylate.
In order for the prism layer or lens layer to have a high refractive index, it is preferable to use a high bridged type compound having the above-mentioned multifunctional monomer as the principle component. Typically, a non-solvent type ionizing radiation setting resin is used. However, depending on requirements, it is acceptable to use the one that is diluted in a solvent.
Examples of the above-mentioned resin film that can be used together with the ionizing radiation setting resin include a polyester resin such as polyethyleneterephtalate, an acrylic resin such as polymethyl(meta)acrylate, and films made of polycarbonate, polyarylate, polyimide, polypropylene, or fluororesin.
To cure the ionizing radiation setting resin with ultraviolet radiation, a photopolymerization initiator, such as an acetophenone class or benzophenone class, and/or a photosensitization agent, such as n-butylamine, triethylamine or tri-n-butylphosphine, are appropriately added in the resin.
Curing of the ionizing radiation setting resin is normally conducted by irradiating the resin with an electron beam or ultraviolet radiation. When the electron beam is used for the curing, the electron beam needs to have an energy level ranging from 50 to 1000 ke V, or more preferably from 100 to 300 ke V. Such an electron beam can be obtained from an electron beam accelerator, such as Cockroft-Walton's type, Van De Graaf type, resonance transformation type, insulated core transformation type, linear type, dynamitron type, or high-frequency type. For ultraviolet-setting, ultraviolet rays from a light source, such as a very high-pressure mercury-arc lamp, a high-pressure mercury-arc lamp, a low-pressure mercury-arc lamp, a carbon arc, a xenon arc, or a metal halide lamp, can be used.
Referring to
A standard anti-reflection layer may be used for this purpose. Alternatively, a multi-layer film formed by alternatively laminating low refractive index layers and high refractive index layers with the low refractive index layer on the front side may be used as the anti-reflection layer. Such low refractive index layers may be formed by vacuum deposition, sputtering, or plasma chemical vapor deposition (CVD) of a low refractive index material, or by coating a coating solution having a powder-state low refractive index material in a resin binder. The high refractive index layers may be formed by vacuum deposition, sputtering, or plasma CVD of a high refractive index material, or by coating a coating solution having a powder-state high refractive index material in a resin binder. In view of the anti-reflection effect, it is desirable that the thickness of the low refractive index layer be about 0.1 μm and that the thickness of the high refractive index layer also be about 0.1 μm.
If the surface on which the anti-reflection layer is formed is an uneven surface, such as a prism surface or lens surface, the anti-reflection layer may be formed by a coating method, such as dipping method or spraying method, or by a thin-film forming method, such as vacuum vapor deposition, sputtering, or plasma CVD.
For the low refractive index material, inorganic compounds, such as LiF, MgF2, 3NaF.AlF3, AlF3, Na3.AlF6 or SiOx (1.50≦×≦2.00) (refractive index of 1.35 to 1.48), may be used. When included in the resin binder, ultra-micro particles with a diameter of 5 nm to 50 nm may be used.
In addition, a low refractive index organic compound, such as a low refractive index thermoplastic resin (polymer), may be added to the resin binder in addition to the above-mentioned ultra-micro particles to adjust the refractive index of the low refractive index layer. Examples of such a low refractive index thermoplastic resin are fluororesins obtained by homopolymerization of fluorine inclusive monomers, such as CF2═CF2, CH2═CH2, and CF2═CHF, or by copolymerization, block polymerization or graft polymerization of two or more kinds of monomers. For example, PTFE (poly4ethylene fluoride), PVDF (polyvinylidene fluoride), and PVF (polyvinyl fluoride) are desirable because their refractive index is low: 1.45 or less. As the low refractive index material described above, it is also possible to make the resin binder itself have a low refractive index by including fluoride in the molecules of the compound that constitutes the resin binder.
For the high refractive index material, inorganic compounds, such as ZnO, TiO2, CeO2, Sb2O5, SnO2, ITO (Indium Tin Oxide), Y2O3, La2O3l , ZrO2, or Al2O3, can be used. When the material is to be included in a resin binder, the corresponding ultra-micro particles are used.
In addition, when a resin binder is used for the high refractive index layer, the resin binder itself can have a high refractive index by including the halogen group (except fluoride), sulfur, nitrogen, or phosphorus in the molecules of the compound that constitutes the resin binder.
An ionizing radiation setting resin can be used as a resin binder for the formation of the low refractive index layer and the high refractive index layer. Known ionizing radiation setting resins includes ultraviolet setting resins or electron beam setting resins, represented by, for example, compounds made from prepolymers and/or monomers that have a polymerization function group, such as a (meta)acryloyl group, (meta)acryloyloxy group, epoxy group, or mercapto group, in the constituent molecules. Examples of compounds that can be used are made by adding an appropriate reactive dilution to a prepolymer, such a urethane(meta) acrylate, epoxy(meta)acrylate, or silicon(meta)acrylate. The reactive dilution may be a monofunctional monomer, such as ethyl(meta)acrylate, ethylhexyl(meat)acrylate, styrene, methystyrene, or N-vinylpyrrolidene, or a multifunctional monomer, such as trimethylolpropanetri(meta)acrylate, hexanediol(meta)acrylate, tripropyleneglycoldi(meta) acrylate, diethyleneglycoldi(meta)acrylate, pentaerythritoltri(meta)acrylate, dipentaerythritolhexa (meta)acrylate, 1,6-hexanedioldi(meta)acrylate, and neopentylglycoldi(meta)acrylate.
For producing a low refractive index, it is desirable to have less multifunctional monomers, which are desirable to use if the film lacks a sufficient elasticity. When a fluoride inclusive monomer, such as trifluoroethylacrylate (refractive index of 1.32), is used, the resin binder itself can have a low reflective index. Trifluoroethylacrylate is a monofunctional monomer, and when its homopolymer has a weak film strength, a multifunctional monomer, such as dipentaerythritolhexaacrylate, may be added. However, when the multifunctional monomer is added, the refractive index increases. Therefore, the concentration of such a multinational monomer is desirably within the range of 1 to 50 parts by weight for every 100 parts by weight of the monofunctional monomer, or more preferably, within the range of 5 to 20 parts by weight.
The above-mentioned ionizing radiation setting resin may be used without a solvent or diluted in a solvent, depending on the need.
An example of the ionizing radiation setting resin is a mixture of polyester acrylate and polyurethane acrylate. The resultant film has a strength, flexibility, and impact durability. The mixing ratio preferably is 30 or less parts by weight of polyurethaneacrylate for every 100 parts by weight of polyesteracrylate to produce sufficient hardness.
In addition, when a setting resin is cured with ultraviolet rays, in a fashion similar to the ionizing radiation setting resin used in the lens layer and prism layer described above, a photopolymerization initiator and photosensitization agent can be appropriately added to the resin. The curing process can be conducted by irradiating the resin with electron beams or ultraviolet rays in a similar manner.
Known resin based films can be used as such a polarizing film. For example, it is possible to form the film using a method in which iodine and/or a dichroistic dye is adsorbed and oriented on a hydrophilic film, such as a polyvinylalcohol system film or a partially formal polyvinylalohol film, an ethylene-vinylacetate copolymer system saponificated film, and a cellulose system film, or using a method of forming polyene by performing a dehydration process on a polyvinylalcohol system film.
By adding the polarizing layer 8 to the polarization light splitting film, as described above, a polarizer plate on the light incident side of a liquid crystal cell, which is normally required to produce a linearly polarized light beam, can be omitted. In this case, it is of course necessary to match the polarization axis of polarizing layer 8 with the polarization axis of the linearly polarized light emitted from the quarter-wave layer 2.
If a polarization light splitting film does not include a polarizing layer, as in the previous embodiments, the polarization axis of the quarter-wave layer (the polarization axis of linearly polarized light emitted from that layer) should be matched with the polarization axis of a liquid crystal cell that is to be coupled to the polarization light splitting film.
The above-mentioned layers may be laminated on a base member having a sufficient strength such as substrate 3 in FIG. 2. Also, it is possible to adhere the layers together using a cement layer or an adhesive layer in between.
For the cement used for the cement layer, it is desirable to use urethane system cements, for example, reactive-setting type urethane system cements, such as humidity-setting types (1-liquid type) or thermosetting types (2-liquid type). The humidity-setting types are used in combination with an oligomer and/or a prepolymer of a polyisocyanate compound. The thermosetting-types are used in combination with an oligomer and/or a prepolymer of a polyol compound and with a monomer, oligomer, and/or prepolymer of a polyisocynate compound. For these reactive-setting-type urethane system cements, when the aging process is conducted after the lamination, it is desirable to conduct it in the temperature range from a room temperature to 80 degrees centigrade. For the adhesive used for the adhesive layer, known adhesive compounds of acrylic resin-type can be used.
On the polarization light splitting film with the laminated structure, a hard coat layer, an adhesive layer, or a cement layer can be formed depending on their needs. Here, the hard coat layer represents a layer having a hardness of H or higher in the pencil hardness test based on JIS (Japanese Industrial Standards) K5400. The hard coat layer can be formed from either inorganic materials or organic materials. An example of an inorganic material that can be used is a complex oxide film formed by a sol-gel method. Organic materials that can be used include a transparent resin film of a thermoplastic resin, and more preferably, a reactive-setting resin, such as a thermosetting resin or ionizing radiation setting resin. The ionizing radiation setting resin is more preferable. For the thermosetting resin, a phenol resin, urea resin, diallylphtalate resin, melamine resin, guanamine resin, unsaturated polyester resin, polyurethane resin, epoxy resin, aminoalkyd resin, melamine-urea copolycondensated resin, silicon resin, or polysiloxane resin can be used. Depending on the requirements of these resins, the hard coat layer is coated with a coating solution that includes a bridging agent or polymerization initiator as a setting agent, a polymerization accelerator, a solvent, and a viscosity adjustment agent.
For the ionizing radiation setting resin, the resins used for the prism layer, lens layer, low refractive index layer, and high refractive index layer described above can be used. To add flexibility to the hard coat layer of the ionizing radiation setting resin, it is acceptable to include 1 to 100 parts by weight of the thermoplastic resin for every 100 parts by weight of the ionizing radiation setting resin. For the thermoplastic resin, if the ionizing radiation setting resin composition is made of polyester acrylate and polyurethane acrylate, polymethylmethacryl acrylate and polybutylmethacryl acrylate are desirable in terms of their transparency, low haze value, high light transmitability, and compatibility. When the resin is cured with ultraviolet radiation, a photopolymerization initiator and a photosensitization agent are appropriately added in the resin in a similar manner to the ionizing radiation setting resin used in the lens layer and prism layer. Similarly, the curing is conducted by irradiation with electron beams or ultraviolet rays. In addition, it is preferable that the thickness of the hard coat layer be about 0.5 μm, or more preferably, about 3 μm or more to maintain necessary hardness.
As the adhesive layer and the cement layer, known materials, such as adhesives with an acrylic resin and cement layers with a urethane system adhesive, can be used, for example.
Next, backlight and liquid crystal devices according to other preferred embodiments of the present invention will be described with reference to
In
In the backlight and liquid crystal device of
In
The material of light guide 22 needs to have the ability to transmit light efficiently but is not limited to a specific class of material. Examples are an acrylic resin, such as PMMA (polymethylmeta acrylate), a polycarbonate resin, and glass. The light guide 22 preferably has a plate-shape or a wedge-shape with the thickness decreasing in a direction away from the light source. Light emitted from the light source 21 travels in the light guide 22 by repeating total internal reflections. The light is also diffused (scattered) by the light diffusion elements 23, and is emitted from the emitting face of the light guide 22.
To form the light diffusion elements 23 in the light guide, the following methods can be used: (1) forming light diffusion elements by dispensing such an agent as silica in a resin in a dot pattern on the light emitting face or on the other (bottom) face of the light guide 23 by a printing or like method (
For reflective sheet 24, a white plastic sheet or a plastic sheet having aluminum vapor-deposited thereon, can be used.
In the structure shown in
As for the arrangement of the diffusion film and prism sheet, instead of placing the diffusion film and prism sheet in that order from the emitting surface side of the light guide, the order of the arrangement may be the prism sheet and then the diffusion film. Multiple layers of diffusion film and prism sheets may also be used. The arrangement of the diffusion films and the prism sheets is not limited by use of the polarization light splitting film of the present invention.
The diffusion film may be formed by molding a polymer film using the embossing method or the like for forming a rough surface or by distributing beads or fillers of an organic or inorganic material in the resin.
The prism sheets function properly, as long as the material has efficient light transmissibility. Examples of such a material include polycarbonate (PC), polyester resins such as polyethylene terephtalate (PET), acrylic resins such as polymethyl metacrylate (PMMA), and glass. In particular, prism sheets created by forming a prism-shape layer on a base film made of PET or PC using an ultraviolet-setting resin are preferable since micro prism-shape structure can be accurately formed and this forming method is suitable for mass production. In this case, the refractive index of the prism-shape layer made of the ultraviolet-setting resin is preferably about 1.4 or larger, or more preferably, about 1.5 or larger. To form the prism shape layer with the ultraviolet-setting resin on the base film, it is desirable to utilize a method disclosed in Laid-Open Japanese Patent Application No. 05-169015. In this method, the ultraviolet-setting resin is coated on an intaglio roll that has recessed patterns corresponding to the prism shape to be manufactured, and a base film is pressed on the intaglio roll having the resin solution on the printing surface. Then, the intaglio roll is irradiated with ultraviolet radiation to cure the resin. Thereafter, the cured ultraviolet-setting resin is peeled off from the intaglio roll together with the base film. By this method, the prism sheet can be continuously manufactured.
As descried with reference to
Working examples of the present invention will now be described with reference to the drawings.
As the optical rotation selection layer, a cholesteric liquid crystal polymer film (having the helical axis of the liquid crystal along a direction of the thickness and showing superior circular dichroism with respect to visible light) with a thickness of 15 μm was formed by photopolymerization with ultraviolet irradiation. A phase-differentiation film made by Sumitomo Chemical Co., Ltd. product name “SUMILITE” with a thickness of 60 μm, was used as the quarter-wave layer. The resultant optical rotation selection layer and quarter-wave layer were adhered to each other with an adhesive compound to form the polarization light splitting film. See
A cholesteric liquid crystal polymer film with a thickness of 2 μm was formed on a glass base by photopolymerization with ultraviolet irradiation. By grinding the cholesteric liquid crystal polymer film, a filler of the cholesteric liquid crystal polymer, each molecule having a fish-scale-like shape with about 20 μm in average diameter, was obtained. The filler was dispersed into a solvent solution of acrylic resin to yield a coating solution. The coating solution was coated on a polyethyleneterephtalate film base of a thickness of 50 μm to form a cholesteric liquid crystal layer of thickness 20 μm (in dry) thereon. An optical rotation selection layer of this working example corresponds to the film base and the cholesteric liquid crystal layer. The quarter-wave film of the first working example above was adhered on the cholesteric liquid crystal layer in a manner similar to that of the first working example to complete the polarization light splitting film of the present working example. See
In a third working example of the polarization light splitting film, a diffusion layer with an average thickness of 20 μm (in dry) was additionally formed on the polyethyleneterephtalate film side (light receiving side) surface of the optical rotation selection layer of the second working example above. The diffusion layer was formed by coating a diffusion coat on the surface using a rolling coater. The diffusion coat was prepared mixing acrylic resin beads with the average particle diameter of 10 μm as a diffusion agent with a polyester resin, an isocyanate setting agent, and a solvent. See
A polarization light splitting film according to a fourth working example of the present invention has an anti-reflection layer attached to the light receiving surface (polyethyleneterephtalate film surface) of the polarization light splitting film of the second working example above. The anti-reflection layer was manufactured by forming a hard coat layer with a thickness of 5 μm having a high refractive index on the polyethyleneterephtalate film surface of the second working example and then forming a low refractive index layer with a thickness of 0.1 μm on the hard coat layer. To form the hard coat layer, a solution of acrylate having a carboxyl group with ultra-micro particles of ZrO2 was coated on the polyethyleneterephtalate film surface and is cured with electron beam irradiation. The low refractive index layer was formed by depositing SiO2 (refractive index: about 1.46) on the hard coat layer by vapor deposition.
Various film bases having uneven surface profiles were manufactured to serve as a prism layer or lens layer for supporting the optical rotation selection layer, as follows.
First, an uneven surface profile was formed on a copper plated surface of a cylindrical block with a plurality of unit elements arranged at a 50 μm pitch and by plating the resultant surface with chrome. The resultant cylindrical block serves as an intaglio roll for forming a film base. Each of the unit elements on the intaglio roll has a predetermined surface profile that is in a reciprocal relationship with the surface profile of each of the unit elements disposed on the film base to be manufactured. Various intaglio rolls were manufactured to form various prism layers and lens layers. Cutting processes with a diamond bit were used for forming the surface profiles of an isosceles triangle with an apex angle of about 90 degrees (corresponding to a fifth working example: see FIG. 5A), a semi-circular column shape (corresponding to a sixth working example: see FIG. 7A), and an inverse semi-circular column shape (corresponding to a seventh working example: see FIG. 7B), before plating chrome on the respective cylindrical blocks. A machine engraving processor is used for forming the quadrangular pyramid shape (corresponding to an eighth working example: see
Using the thus manufactured rolling intaglios as embossing plates, the respective film bases each serving as a prism layer or a lens layer were created by embossing a polycarbonate film having a thickness of 100 μm by thermal pressing. Using each of the film bases as the substrate 3 for supporting the optical rotation selection layer of the second working example (with the cholesteric liquid crystal layer formed on the surface of the film base opposite to the uneven surface), the corresponding working examples (fifth to ninth) were completed.
In these working examples, film bases having uneven surface profiles corresponding to the fifth to ninth working examples above were manufactured by a different method. The tenth to fourteen working examples respectively correspond to the fifth to ninth working examples.
In these working examples, instead of using embossment, an ultraviolet setting resin was used to form the uneven surface profiles of the film bases corresponding to the fifth to ninth working examples. A urethane resin system primer was applied on a polyethyleneterephtalate film with a thickness of 100 μm and was thermally cured to form a primer layer with a thickness of 1 μm on the polyethyleneterephtalate film.
An ultraviolet setting resin solution with an epoxy acrylate system as the primary component was coated on the corresponding rotating intaglio roll. Then, the composite film obtained above was pressed onto the intaglio roll with the ultraviolet setting solution and irradiated with ultraviolet radiation to cure the resin solution. The solidified ultraviolet setting resin is peeled off along with the film from the rotating intaglio roll. A film base that serves as a prism layer or lens layer made of cured ultraviolet setting resin on the primer layer is thereby created. This film base is used as the base for the optical rotation selection layer in the second working example. By forming a cholesteric liquid crystal layer on the surface of the resultant film base opposite to its uneven surface, the polarization light splitting film was completed.
A polarizing film with a thickness of 120 μm (made by Sumitomo Chemical Co., Ltd., product name, “SUMILITE”) was adhered on the quarter-wave layer of the second working example above (i.e., on the light emitting side). See
Evaluations
The transmissivity of polarized light, haze, and the luminance of the backlight were measured using the following methods. The results are listed in Tables 1 and 2.
TABLE 1
Measurement results for the
polarized light transmission factor and haze
Working Example
T⊥ (%)
T∥ (%)
Haze (%)
1
10
75
5
2
10
80
3
3
5
65
30
4
5
82
10
5
5
80
10
6
5
80
10
7
5
80
10
8
5
80
10
9
5
80
10
10
5
83
5
11
5
83
5
12
5
83
5
13
5
83
5
14
5
83
5
15
0.5
35
3
TABLE 2
Measurement results for luminance
Luminance in
the normal
(cd/cm2)
Polarization light splitting film (Working Example 15)
85
Standard polarizing plate
70
As shown in Tables 1 and 2, each embodiment had satisfactory results for the polarization linearity and the haze value. The luminance was improved by approximately 20% (=(85−70)/70×100).
As described above, according to the present invention, the light usage efficiency of the backlight system can be improved with a relatively simple structure. In addition, due to its relatively simple structure, the polarization light splitting film of the present invention has superior mass production capability. Also, it has a planar shape and is suited for designing thin backlight systems and thin liquid crystal display devices.
In addition, by equipping the polarization light splitting film according to the present invention with functional layers, such as a diffusion layer, prism layer, lens layer, and polarizing layer, it becomes possible to assemble a backlight system having a simple structure.
Furthermore, the backlight and liquid crystal device using the polarization light splitting film of the present invention can easily be made thin. Additionally, when a polarization light splitting film includes the functional layers, the system construction is simplified and complicated assembly processes are not necessary.
It will be apparent to those skilled in the art that various modifications and variations can be made in the polarization light splitting film of the present invention without departing from the spirit or scope of the invention. Thus, it is intended that the present invention cover the modifications and variations of this invention provided they come within the scope of the appended claims and their equivalents.
Arakawa, Fumihiro, Kashima, Keiji
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