WO2015080167A1

WO2015080167A1 - Cycloolefin-based resin composition film

Info

Publication number: WO2015080167A1
Application number: PCT/JP2014/081279
Authority: WO
Inventors: 慶小幡; 堀井　明宏; 石森　拓; 健細谷; 香奈子橋本; 一樹平田
Original assignee: デクセリアルズ株式会社
Priority date: 2013-11-26
Filing date: 2014-11-26
Publication date: 2015-06-04
Also published as: TW201527398A; JP2015101682A

Abstract

A cycloolefin-based resin composition film which exhibits excellent preservation stability against environmental changes and excellent toughness is provided. This composition film comprises both a cycloolefin-based resin (11) and a styrene-based elastomer (12) which exhibits a melt flow rate of 4.5g/10min or less as determined according to ISO 1133 at 230ºC under a load of 2.16kgf. The styrene-based elastomer (12) is dispersed in the cycloolefin-based resin (11) with the content of the elastomer (12) being 5 to 35wt%, and the minor axis diameters of the dispersed particles of the styrene-based elastomer (12) are 2μm or less. Thus, excellent preservation stability against environmental changes and excellent toughness can be attained.

Description

Cyclic olefin resin composition film

The present invention relates to a cyclic olefin resin composition film in which an elastomer or the like is added and dispersed in a cyclic olefin resin. This application claims priority on the basis of Japanese Patent Application No. 2013-244425 filed on November 26, 2013 in Japan. This application is incorporated herein by reference. Incorporated.

Cyclic olefin resin is an amorphous and thermoplastic olefin resin that has a cyclic olefin skeleton in its main chain, has excellent optical properties (transparency, low birefringence), low water absorption, It has excellent performance such as dimensional stability and high moisture resistance. Therefore, films or sheets made of cyclic olefin resins are expected to be developed for various optical applications such as retardation films, polarizing plate protective films, light diffusion plates, and moisture proof packaging applications such as pharmaceutical packaging and food packaging. Yes.

Since the film of cyclic olefin resin is inferior in toughness, it is known to improve toughness by adding and dispersing an elastomer having a hard segment and a soft segment (for example, see Patent Document 1). However, the segment of the elastomer changes phase due to environmental changes, and even if the environment is returned to room temperature, it does not return to the original state. Therefore, the environmental preservation of the cyclic olefin resin film deteriorates due to the change in haze.

JP 2004-156048 A

The present invention has been proposed in view of such a conventional situation, and provides a cyclic olefin-based resin composition film having excellent environmental preservation and toughness.

The present inventor has found that by adding a styrene elastomer having a specific melt flow rate to a cyclic olefin resin at a specific dispersion diameter, environmental preservation can be improved while maintaining excellent toughness, The present invention has been completed.

That is, the cyclic olefin-based resin composition film according to the present invention has a cyclic flow olefin-based resin and a melt flow rate measured under conditions of 230 ° C. and 2.16 kgf in accordance with ISO 1133 of 4.5 g / 10 min or less. A styrene-based elastomer, wherein the styrene-based elastomer is dispersed in an amount of 5 to 35 wt% in the cyclic olefin-based resin, and the minor axis dispersion diameter of the styrene-based elastomer is 2 μm or less. .

Moreover, the manufacturing method of the cyclic olefin-type resin composition film which concerns on this invention is based on cyclic olefin-type resin and ISO1133, and the melt flow rate measured on condition of 230 degreeC and 2.16kgf is 4.5 g / A styrene elastomer that is 10 min or less is melted at a temperature in the range of 210 ° C. to 300 ° C., and the molten cyclic olefin resin composition is extruded into a film by an extrusion method. A cyclic olefin resin composition film obtained by dispersing 5 to 35 wt% in an olefin resin and having a short axis dispersion diameter of the styrene elastomer of 2 μm or less is obtained.

Also, the cyclic olefin resin composition film according to the present invention is suitable for application to transparent conductive elements, input devices, display devices, and electronic devices.

According to the present invention, when the short axis dispersion diameter of the styrene elastomer having a specific melt flow rate dispersed in the cyclic olefin resin is 2 μm or less, excellent environmental preservation and toughness can be obtained. .

FIG. 1 is a cross-sectional perspective view showing an outline of a cyclic olefin-based resin composition film according to the present embodiment. FIG. 2 is a cross-sectional photograph of a film for explaining an example of a method for measuring the minor axis dispersion diameter. FIG. 3 is a schematic diagram illustrating a configuration example of a film manufacturing apparatus. 4A and 4B are cross-sectional views illustrating an example of a transparent conductive film, and FIGS. 4C and 4D are cross-sectional views illustrating an example of a transparent conductive film provided with a moth-eye-shaped structure. FIG. 5 is a schematic cross-sectional view illustrating a configuration example of the touch panel. FIG. 6 is an external view illustrating an example of a television device as an electronic apparatus. 7A and 7B are external views illustrating an example of a digital camera as an electronic device. FIG. 8 is an external view illustrating an example of a notebook personal computer as an electronic device. FIG. 9 is an external view illustrating an example of a video camera as an electronic apparatus. FIG. 10 is an external view illustrating an example of a mobile phone as an electronic device. FIG. 11 is an external view illustrating an example of a tablet computer as an electronic device.

Hereinafter, embodiments of the present invention will be described in detail in the following order with reference to the drawings.
1. 1. Cyclic olefin resin composition film 2. Production method of cyclic olefin-based resin composition film 3. Application example to electronic equipment Example

<1. Cyclic Olefin Resin Composition Film>
The cyclic olefin-based resin composition film according to the present embodiment has a cyclic flow olefin-based resin and a melt flow rate measured under conditions of 230 ° C. and 2.16 kgf in accordance with ISO 1133 of 4.5 g / 10 min or less. The styrene elastomer contains 5 to 35 wt% in a cyclic olefin resin, and the minor axis dispersion diameter of the styrene elastomer is 2 μm or less. Thereby, the outstanding environmental preservation property and toughness can be obtained.

FIG. 1 is a cross-sectional perspective view showing an outline of a cyclic olefin-based resin composition film according to the present embodiment. The cyclic olefin-based resin composition film is, for example, a short film or sheet, the X-axis direction which is the width direction (TD: Transverse Direction), and the Y-axis direction which is the length direction (MD: Machine Direction), And a Z-axis direction that is a thickness direction. The thickness Z of the cyclic olefin-based resin composition film is preferably 0.1 μm to 2 mm, more preferably 1 μm to 1 mm.

The cyclic olefin-based resin composition film contains a cyclic olefin-based resin 11 and a styrene-based elastomer 12, and the styrene-based elastomer 12 is dispersed in the cyclic olefin-based resin 12 by 5 to 35 wt%. That is, the mass% ratio of cyclic olefin resin / styrene elastomer is 95/5 to 65/35 (the total of both is 100 mass%). A more preferable mass% ratio of cyclic olefin resin / styrene elastomer is 93/7 to 80/20. If the addition ratio of the styrene-based elastomer 12 is too large, the environmental preservation is reduced, and if it is too small, the toughness is not sufficient.

Further, in the cyclic olefin resin composition film, a dispersed phase (island phase) made of styrene elastomer 12 is dispersed in a matrix (sea phase) made of cyclic olefin resin 11. The dispersed phase is dispersed with shape anisotropy in the MD direction by, for example, extrusion molding, has a major axis in the MD direction, and a minor axis in the TD direction.

The short axis dispersion diameter of the styrene elastomer 12 is 2 μm or less, more preferably 1 μm or less. If the minor axis dispersion diameter is too large, a gap is generated between the styrene elastomer / cyclic olefin resin due to the styrene elastomer phase change under environmental preservation, and the refractive index of the styrene elastomer itself changes, The haze of the entire film is greatly changed.

In the present specification, the short axis dispersion diameter means the size in the TD direction of the dispersed phase composed of the styrene elastomer 12 and can be measured as follows. First, the TD-thickness (Z-axis) cross section of the cyclic olefin-based resin composition film is cut. And as shown in FIG. 2, the film cross section is enlarged and observed, the short axis of each disperse phase of the predetermined range of the film cross section center is measured, and the average value is made into a short axis dispersion diameter. Moreover, when a dispersion diameter is small, it is preferable to cut | disconnect, after giving osmium dyeing | staining with respect to a film.

Hereinafter, the cyclic olefin resin and the styrene elastomer will be described in detail.

[Cyclic olefin resin]
The cyclic olefin-based resin is a polymer compound having a main chain composed of carbon-carbon bonds and having a cyclic hydrocarbon structure in at least part of the main chain. This cyclic hydrocarbon structure is introduced by using a compound (cyclic olefin) having at least one olefinic double bond in the cyclic hydrocarbon structure as represented by norbornene or tetracyclododecene as a monomer. Is done.

Cyclic olefin resins include cyclic olefin addition (co) polymers or hydrogenated products thereof (1), cyclic olefin and α-olefin addition copolymers or hydrogenated products (2), cyclic olefin ring-opening ( Co) polymers or hydrogenated products thereof (3).

Specific examples of the cyclic olefin include: cyclopentene, cyclohexene, cyclooctene; one-ring cyclic olefin such as cyclopentadiene, 1,3-cyclohexadiene; bicyclo [2.2.1] hept-2-ene (common name: norbornene) ), 5-methyl-bicyclo [2.2.1] hept-2-ene, 5,5-dimethyl-bicyclo [2.2.1] hept-2-ene, 5-ethyl-bicyclo [2.2. 1] Hept-2-ene, 5-butyl-bicyclo [2.2.1] hept-2-ene, 5-ethylidene-bicyclo [2.2.1] hept-2-ene, 5-hexyl-bicyclo [ 2.2.1] hept-2-ene, 5-octyl-bicyclo [2.2.1] hept-2-ene, 5-octadecyl-bicyclo [2.2.1] hept-2-ene, 5- Metilide -Bicyclo [2.2.1] hept-2-ene, 5-vinyl-bicyclo [2.2.1] hept-2-ene, 5-propenyl-bicyclo [2.2.1] hept-2-ene Bicyclic olefins such as;

Tricyclo [4.3.0.1 ^2,5 ] deca-3,7-diene (common name: dicyclopentadiene), tricyclo [4.3.0.1 ^2,5 ] dec-3-ene; tricyclo [ 4.4.0.1 ^2,5 ] undeca-3,7-diene or tricyclo [4.4.0.1 ^2,5 ] undeca-3,8-diene or a partially hydrogenated product thereof (or cyclopentadiene) Tricyclo [4.4.0.1 ^2,5 ] undec-3-ene; 5-cyclopentyl-bicyclo [2.2.1] hept-2-ene, 5-cyclohexyl-bicyclo [2.2.1] hept-2-ene, 5-cyclohexenylbicyclo [2.2.1] hept-2-ene, 5-phenyl-bicyclo [2.2.1] hept-2-ene A cyclic olefin of the ring;

Tetracyclo [4.4.0.1 ^2,5 . 1 ^7,10 ] dodec-3-ene (also simply referred to as tetracyclododecene), 8-methyltetracyclo [4.4.0.1 ^2,5 . 1 ^7,10 ] dodec-3-ene, 8-ethyltetracyclo [4.4.0.1 ^2,5 . 1 ^7,10 ] dodec-3-ene, 8-methylidenetetracyclo [4.4.0.1 ^2,5 . 1 ^7,10 ] dodec-3-ene, 8-ethylidenetetracyclo [4.4.0.1 ^2,5 . 1 ^7,10 ] dodec-3-ene, 8-vinyltetracyclo [4.4.0.1 ^2,5 . 1 ^7,10 ] dodec-3-ene, 8-propenyl-tetracyclo [4.4.0.1 ^2,5 . 1 ^7,10 ] tetracyclic olefins such as dodec-3-ene;

8-cyclopentyl-tetracyclo [4.4.0.1 ^2,5 . 1 ^7,10 ] dodec-3-ene, 8-cyclohexyl-tetracyclo [4.4.0.1 ^2,5 . 1 ^7,10 ] dodec-3-ene, 8-cyclohexenyl-tetracyclo [4.4.0.1 ^2,5 . 1 ^7,10 ] dodec-3-ene, 8-phenyl-cyclopentyl-tetracyclo [4.4.0.1 ^2,5 . 1 ^7,10 ] dodec-3-ene; tetracyclo [7.4.1 ^3,6 . 0 ^1,9 . 0 ^2,7 ] tetradeca-4,9,11,13-tetraene (also referred to as 1,4-methano-1,4,4a, 9a-tetrahydrofluorene), tetracyclo [8.4.1 ^4,7 . 0 ^1,10 . 0 ^3,8 ] pentadeca-5,10,12,14-tetraene (also referred to as 1,4-methano-1,4,4a, 5,10,10a-hexahydroanthracene); pentacyclo [6.6.1] ^.1,3,6 . 0 ^2,7 . 0 ^9,14 ] -4-hexadecene, pentacyclo [6.5.1.1 ^3,6 . 0 ^2,7 . 0 ^9,13] -4-pentadecene, pentacyclo [7.4.0.0 ^2,7. 1 ^3,6 . 1 ^10,13] -4-pentadecene; heptacyclo [8.7.0.1 ^2,9. 1 ^4,7 . 1 ^{11, 17} . 0 ^3,8 . 0 ^12,16 ] -5-eicosene, heptacyclo [8.7.0.1 ^2,9 . 0 ^3,8 . 1 ^4,7 . 0 ^12,17 . 1 ^13,16 ] ^-14-eicosene ; and polycyclic cyclic olefins such as cyclopentadiene tetramer. These cyclic olefins can be used alone or in combination of two or more.

Specific examples of the α-olefin copolymerizable with the cyclic olefin include ethylene, propylene, 1-butene, 1-pentene, 1-hexene, 3-methyl-1-butene, 3-methyl-1-pentene, 3 -Ethyl-1-pentene, 4-methyl-1-pentene, 4-methyl-1-hexene, 4,4-dimethyl-1-hexene, 4,4-dimethyl-1-pentene, 4-ethyl-1- Hexene, 3-ethyl-1-hexene, 1-octene, 1-decene, 1-dodecene, 1-tetradecene, 1-hexadecene, 1-octadecene, 1-eicosene, etc. 2-20, preferably carbon numbers Examples thereof include 2 to 8 ethylene or α-olefin. These α-olefins can be used alone or in combination of two or more. As these α-olefins, those contained in the range of 5 to 200% with respect to the cyclic polyolefin can be used.

There is no particular limitation on the polymerization method of the cyclic olefin or the cyclic olefin and the α-olefin and the hydrogenation method of the obtained polymer, and it can be carried out according to a known method.

In the present embodiment, an addition copolymer of ethylene and norbornene is preferably used as the cyclic olefin resin.

The structure of the cyclic olefin-based resin is not particularly limited, and may be a chain, branched, or crosslinked, but is preferably a straight chain.

The molecular weight of the cyclic olefin-based resin is 5,000 to 300,000, preferably 10,000 to 150,000, and more preferably 15,000 to 100,000 according to the GPC method. If the number average molecular weight is too low, the mechanical strength decreases, and if it is too high, the moldability deteriorates.

In addition, the cyclic olefin resin has a polar group (for example, a carboxyl group, an acid anhydride group, an epoxy group, an amide group, an ester group, a hydroxyl group, etc.) in the above-mentioned cyclic olefin resins (1) to (3). What (4) which grafted and / or copolymerized the unsaturated compound (u) which has can be included. Two or more of the above cyclic olefin resins (1) to (4) may be used in combination.

Examples of the unsaturated compound (u) include (meth) acrylic acid, maleic acid, maleic anhydride, itaconic anhydride, glycidyl (meth) acrylate, alkyl (meth) acrylate (carbon number 1 to 10) ester, maleic acid Examples include alkyl (having 1 to 10 carbon atoms) ester, (meth) acrylamide, (2-hydroxyethyl) (meth) acrylate, and the like.

Affinity with metals and polar resins can be increased by using a modified cyclic olefin resin (4) obtained by grafting and / or copolymerizing an unsaturated compound (u) having a polar group, so vapor deposition, sputtering, coating It is possible to increase the strength of various secondary processing such as adhesion, and is suitable when secondary processing is required. However, the presence of the polar group has a drawback of increasing the water absorption rate of the cyclic olefin resin. Therefore, the content of polar groups (for example, carboxyl group, acid anhydride group, epoxy group, amide group, ester group, hydroxyl group, etc.) is preferably 0 to 1 mol / kg per 1 kg of cyclic olefin resin.

[Styrene elastomer]
The styrene-based elastomer has a melt flow rate of 4.5 g / 10 min or less measured under conditions of 230 ° C. and 2.16 kgf in accordance with ISO 1133. If the melt flow rate is large and the molecular weight is too small, the elastomer itself is likely to undergo a phase change under environmental preservation, a gap is formed between the elastomer / cyclic olefin, and the refractive index of the elastomer itself changes, resulting in the entire film Will greatly change the haze.

Further, the melt flow rate of the styrene elastomer is preferably 0.5 g / 10 min or more, and more preferably 1.0 g / 10 min or more. When the melt flow rate is small and the molecular weight is too large, the thermal shrinkage of the elastomer itself becomes large under environmental preservation, and as a result, the haze of the entire film is greatly changed.

The molecular weight of the styrene elastomer is 5,000 to 300,000, preferably 10,000 to 150,000, more preferably 20,000 to 100,000, as determined by the GPC method. If the number average molecular weight is too low, the mechanical strength decreases, and if it is too high, the moldability deteriorates.

The styrene-based elastomer is a copolymer of styrene and a conjugated diene such as butadiene or isoprene and / or a hydrogenated product thereof. The styrene elastomer is a block copolymer having styrene as a hard segment and conjugated diene as a soft segment, and does not require a vulcanization step and is preferably used. Further, the hydrogenated one is more preferable because it has higher thermal stability.

Examples of styrenic elastomers include styrene / butadiene / styrene block copolymers, styrene / isoprene / styrene block copolymers, styrene / ethylene / butylene / styrene block copolymers, and styrene / ethylene / propylene / styrene block copolymers. Examples thereof include styrene and butadiene block copolymers.

In addition, styrene / ethylene / butylene / styrene block copolymer, styrene / ethylene / propylene / styrene block copolymer, styrene / butadiene block copolymer (hydrogenation) in which double bond of conjugated diene component is eliminated by hydrogenation May also be used.

The structure of the styrene-based elastomer is not particularly limited, and may be chain-like, branched or cross-linked, but is preferably linear.

In the present embodiment, at least one styrene selected from the group consisting of styrene / ethylene / butylene / styrene block copolymers, styrene / ethylene / propylene / styrene block copolymers, and hydrogenated styrene / butadiene block copolymers. Based elastomers are preferably used. In particular, hydrogenated styrene / butadiene block copolymers are more preferably used because of high tear strength and small haze increase after environmental preservation. The ratio of butadiene to styrene in the hydrogenated styrene / butadiene block copolymer is preferably in the range of 10 to 90% so as not to impair the compatibility with the cyclic olefin resin.

In addition to the cyclic olefin-based resin and the styrene-based elastomer, various compounding agents may be added to the cyclic olefin-based resin composition as necessary as long as the characteristics are not impaired. The various compounding agents are not particularly limited as long as they are usually used in thermoplastic resin materials. For example, antioxidants, ultraviolet absorbers, light stabilizers, plasticizers, lubricants, antistatic agents, difficulty Examples include flame retardants, colorants such as dyes and pigments, near infrared absorbers, compounding agents such as fluorescent brighteners, and fillers.

According to the cyclic olefin resin composition film having such a configuration, the tear strength can be 60 N / mm or more, preferably 100 N / mm or more, and more preferably 120 N / mm or more. Further, the haze increase after the environmental preservation test can be made 2.0% or less, preferably 1.0% or less. If the tear strength is too smaller than the above range, the film is liable to break during production or use, which is inappropriate. On the other hand, if the change in haze is too worse than the above range, the characteristics will deviate from the initial characteristics in use, and the originally intended characteristics are not satisfied.

<2. Method for Producing Cyclic Olefin Resin Composition Film>
The production method of the cyclic olefin-based resin composition film according to the present embodiment is based on the cyclic olefin-based resin and ISO 1133, and the melt flow rate measured under the conditions of 230 ° C. and 2.16 kgf is 4.5 g / A styrene elastomer that is 10 min or less is melted at a temperature in the range of 210 ° C. to 300 ° C., and the molten cyclic olefin resin composition is extruded into a film by an extrusion method. A cyclic olefin-based resin composition film having a short axis dispersion diameter of styrene-based elastomer of 2 μm or less is obtained. The cyclic olefin-based resin composition film may be non-stretched, uniaxially stretched, or biaxially stretched.

FIG. 3 is a schematic diagram showing a configuration example of a film manufacturing apparatus. The film manufacturing apparatus includes a die 21 and a roll 22. The die 21 is a die for melt molding, and extrudes the molten resin material 23 into a film shape. The resin material 23 contains the above-mentioned cyclic olefin resin composition, for example. The roll 22 has a role of transporting the resin material 23 extruded from the die 21 into a film shape. Further, the roll 22 has a medium flow path therein, and the surface can be adjusted to an arbitrary temperature by an individual temperature control device. Moreover, the material of the surface of the roll 22 is not specifically limited, A metal rubber, resin, an elastomer, etc. can be used.

In the present embodiment, as the resin material 23, a cyclic olefin resin composition containing the above-mentioned cyclic olefin resin and a styrene elastomer is melt-mixed at a temperature in the range of 210 ° C to 300 ° C. As the melting temperature is higher, the minor axis dispersion diameter tends to be smaller.

<3. Application example to electronic equipment>
The cyclic olefin-based resin composition film according to the present embodiment can be used for various optical applications, for example, a retardation film, a polarizing plate protective film, a light diffusion plate, etc., particularly a prism sheet and a liquid crystal cell substrate. Below, the application example which used the cyclic olefin resin composition film as a phase difference film is demonstrated.

4A and 4B are cross-sectional views showing an example of a transparent conductive film. This transparent conductive film (transparent conductive element) is constituted by using the above-mentioned cyclic olefin-based resin composition film as a base film (base material). Specifically, this transparent conductive film includes a retardation film 31 as a base film (base material), and a transparent conductive layer 33 on at least one surface of the retardation film 31. 4A is an example in which the transparent conductive layer 33 is provided on one surface of the retardation film 31, and FIG. 4B is an example in which the transparent conductive layer 33 is provided on both surfaces of the retardation film 31. In addition, as shown in FIGS. 4A and 4B, a hard coat layer 32 may be further provided between the retardation film 31 and the transparent conductive layer 33.

As the material of the transparent conductive layer 33, for example, one or more selected from the group consisting of electrically conductive metal oxide materials, metal materials, carbon materials, and conductive polymers can be used. Examples of metal oxide materials include indium tin oxide (ITO) zinc oxide, indium oxide, antimony-added tin oxide, fluorine-added tin oxide, aluminum-added zinc oxide, gallium-added zinc oxide, silicon-added zinc oxide, and zinc oxide- Examples thereof include a tin oxide system, an indium oxide-tin oxide system, and a zinc oxide-indium oxide-magnesium oxide system. As the metal material, for example, metal nanofillers such as metal nanoparticles and metal nanowires can be used. Specific examples of these materials include copper, silver, gold, platinum, palladium, nickel, tin, cobalt, rhodium, iridium, iron, ruthenium, osmium, manganese, molybdenum, tungsten, niobium, tantalum, titanium, bismuth, Examples thereof include metals such as antimony and lead, and alloys thereof. Examples of the carbon material include carbon black, carbon fiber, fullerene, graphene, carbon nanotube, carbon microcoil, and nanohorn. As the conductive polymer, for example, substituted or unsubstituted polyaniline, polypyrrole, polythiofin, and one or two (co) polymers selected from these can be used.

As a method for forming the transparent conductive layer 33, for example, a PVD method such as a sputtering method, a vacuum deposition method, or an ion plating method, a CVD method, a coating method, a printing method, or the like can be used. The transparent conductive layer 33 may be a transparent electrode having a predetermined electrode pattern. Examples of the electrode pattern include a stripe shape, but are not limited thereto.

As the material of the hard coat layer 32, it is preferable to use an ionizing radiation curable resin that is cured by light or an electron beam, or a thermosetting resin that is cured by heat, and a photosensitive resin that is cured by ultraviolet rays is most preferable. As such a photosensitive resin, for example, acrylate resins such as urethane acrylate, epoxy acrylate, polyester acrylate, polyol acrylate, polyether acrylate, and melamine acrylate can be used. For example, the urethane acrylate resin is obtained by reacting a polyester polyol with an isocyanate monomer or a prepolymer, and reacting an acrylate or methacrylate monomer having a hydroxyl group with the obtained product. The thickness of the hard coat layer 32 is preferably 1 μm to 20 μm, but is not particularly limited to this range.

In addition, as shown in FIGS. 4C and 4D, the transparent conductive film has a moth-eye structure 34 as an antireflection layer on at least one surface of the retardation film. Also good. 4C is an example in which a moth-eye-shaped structure 34 is provided on one surface of the retardation film 31, and FIG. 4D is an example in which a moth-eye-shaped structure is provided on both surfaces of the retardation film. The antireflection layer provided on the surface of the retardation film 11 is not limited to the moth-eye structure described above, and a conventionally known antireflection layer such as a low refractive index layer can also be used. .

FIG. 5 is a schematic cross-sectional view showing one configuration example of the touch panel. The touch panel (input device) 40 is a so-called resistive film type touch panel. The resistive film type touch panel may be either an analog resistive film type touch panel or a digital resistive film type touch panel.

The touch panel 40 includes a first transparent conductive film 41 and a second transparent conductive film 42 facing the first transparent conductive film 41. The 1st transparent conductive film 41 and the 2nd transparent conductive film 42 are bonded together via the bonding part 45 between those peripheral parts. As the bonding part 45, for example, an adhesive paste, an adhesive tape or the like is used. The touch panel 40 is bonded to the display device 44 through the bonding layer 43, for example. As a material of the bonding layer 43, for example, an acrylic, rubber, or silicon adhesive can be used, and an acrylic adhesive is preferable from the viewpoint of transparency.

The touch panel 40 further includes a polarizer 48 bonded to the surface on the touch side of the first transparent conductive film 41 via a bonding layer 50 or the like. As the 1st transparent conductive film 41 and / or the 2nd transparent conductive film 42, the above-mentioned transparent conductive film can be used. However, the retardation film as the base film (base material) is set to λ / 4. By adopting the polarizer 48 and the retardation film 31 in this way, the reflectance can be reduced and the visibility can be improved.

The touch panel 40 is preferably provided with a moth-eye-shaped structure 34 on the opposing surfaces of the first transparent conductive film 41 and the second transparent conductive film 42, that is, on the surface of the transparent conductive layer 33. Thereby, the optical characteristics (for example, a reflection characteristic, a transmission characteristic, etc.) of the 1st transparent conductive film 41 and the 2nd transparent conductive film 42 can be improved.

The touch panel 40 preferably further includes a single-layer or multi-layer antireflection layer on the surface of the first transparent conductive film 41 on the touch side. Thereby, a reflectance can be reduced and visibility can be improved.

It is preferable that the touch panel 40 further includes a hard coat layer on the surface on the touch side of the first transparent conductive film 41 from the viewpoint of improving the scratch resistance. The surface of the hard coat layer is preferably imparted with antifouling properties.

It is preferable that the touch panel 40 further includes a front panel (surface member) 49 bonded to the surface on the touch side of the first transparent conductive film 41 via the bonding layer 51. Moreover, it is preferable that the touch panel 40 further includes a glass substrate 46 bonded to the surface of the second transparent conductive film 42 bonded to the display device 44 via a bonding layer 47.

The touch panel 40 preferably further includes a plurality of structures on the surface to be bonded to the display device 44 of the second transparent conductive film 42 or the like. The adhesion between the touch panel 40 and the bonding layer 43 can be improved by the anchor effect of the plurality of structures. As this structure, a moth-eye structure is preferable. Thereby, interface reflection can be suppressed.

As the display device 44, for example, a liquid crystal display, a CRT (Cathode Ray Tube) display, a plasma display (Plasma Display Panel: PDP), an electroluminescence (Electro Luminescence: EL) display, a surface conduction electron-emitting device display (Surface-conduction Various display devices such as Electron-emitter Display (SED) can be used.

Next, an electronic apparatus including the input device 40 described above will be described. FIG. 6 is an external view illustrating an example of a television device as an electronic apparatus. The television device 100 includes a display unit 101, and the display unit 101 includes a touch panel 40.

7A and 7B are external views showing examples of a digital camera as an electronic device. 7A is an external view of the digital camera viewed from the front side, and FIG. 7B is an external view of the digital camera viewed from the back side. The digital camera 110 includes a light emitting unit 111 for flash, a display unit 112, a menu switch 113, a shutter button 114, and the like, and the display unit 112 includes the touch panel 40 described above.

FIG. 8 is an external view showing an example of a notebook personal computer as an electronic device. The notebook personal computer 120 includes a main body 121 including a keyboard 122 for inputting characters, a display unit 123 for displaying images, and the like, and the display unit 123 includes the touch panel 40 described above.

FIG. 9 is an external view showing an example of a video camera as an electronic device. The video camera 130 includes a main body 131, a subject shooting lens 132 on the side facing forward, a start / stop switch 133 during shooting, a display unit 134, and the like, and the display unit 134 includes the touch panel 40 described above.

FIG. 10 is an external view showing an example of a mobile phone as an electronic device. The mobile phone 140 is a so-called smartphone, and the display unit 141 includes the touch panel 40 described above.

FIG. 11 is an external view showing an example of a tablet computer as an electronic device. The tablet computer 150 includes the touch panel 40 described above on the display unit 151.

Even in each electronic device as described above, since the cyclic olefin resin composition film with little haze change due to the environment is used in the display portion, display with little deterioration over time is possible.

<4. Example>
Examples of the present invention will be described in detail below. In this example, a cyclic olefin-based resin composition film having a short axis dispersion diameter of a styrene-based elastomer was prepared, and tear strength, initial haze, and haze increase were evaluated. The present invention is not limited to these examples.

The short axis dispersion diameter, tear strength, haze, and haze increase were measured as follows.

[Short axis dispersion diameter]
As shown in FIG. 2, the TD (Transverse Direction) -thickness (Z-axis) section of the cyclic olefin-based resin composition film was cut with a microtome, and the film section was magnified and observed about 2500 times with an optical microscope. The short axis of the styrene elastomer in the range of 20 μm × 20 μm in the center of the cross section was measured, and the average value was defined as the short axis dispersion diameter.

The styrene elastomer with a small dispersion diameter is subjected to osmium staining and then sliced with a microtome, and the cross section is magnified and observed at a magnification of about 5000 times with a transmission electron microscope. The minor axis of the styrene elastomer in the range of × 5 μm was measured, and the average value was defined as the minor axis dispersion diameter.

[Tear strength (right-angle tear)]
A film having a thickness of 80 μm was measured according to JISK7128. A No. 3 type test piece was used as a test piece, measured at a test speed of 200 mm / min using a tensile tester (AG-X, manufactured by Shimadzu Corporation), and the average value in the MD and TD directions was determined as the tear strength. did. A tear strength of 60 N / mm or more was evaluated as “◯”, and a tear strength of less than 60 N / mm was evaluated as “x”. If the tear strength is 60 N / mm or more, practical use is possible in that the risk of breakage in a subsequent process such as a coating process is reduced.

[Initial haze and haze rise]
The initial haze of a film having a thickness of 80 μm was measured using a haze meter (HM150, manufactured by Murakami Color Research Laboratory Co., Ltd.). Further, after an environmental preservation test (stored at −40 ° C. for 12 hours and then put into an 85 ° C. oven for 10 minutes), the haze was measured using a haze meter, and the difference from the initial haze was regarded as haze increase. A haze increase of 1.0% or less was evaluated as “◎”, a haze increase of over 1.0% to 2.0% was evaluated as “◯”, and a haze increase of 2.0% Those exceeding were evaluated as “x”.

[Cyclic olefin resin and styrene elastomer]
As the cyclic olefin resin, TOPAS 6013-S04 (manufactured by Polyplastics Co., Ltd., chemical name: addition copolymer of ethylene and norbornene) was used.

Moreover, six types shown in Table 1 were used as the styrene elastomer. Tuftec H1051 (Asahi Kasei Chemicals Corporation) is a styrene / ethylene / butylene / styrene block copolymer having a melt flow rate (230 ° C., 2.16 kgf) measured in accordance with ISO 1133 of 0.8 g / 10 min. It is a coalescence. S. O. E S1605 (manufactured by Asahi Kasei Chemicals Corporation) is a hydrogenated styrene / butadiene block copolymer having a melt flow rate (230 ° C., 2.16 kgf) measured in accordance with ISO 1133 of 3.5 g / 10 min. is there. Tuftec H1221 (manufactured by Asahi Kasei Chemicals Corporation) is a styrene / ethylene / butylene / styrene block copolymer having a melt flow rate (230 ° C., 2.16 kgf) measured according to ISO 1133 of 4.5 g / 10 min. It is a coalescence. Tuftec H1517 (Asahi Kasei Chemicals Co., Ltd.) is a styrene / ethylene / butylene / styrene block copolymer having a melt flow rate (230 ° C., 2.16 kgf) measured in accordance with ISO 1133 of 5.0 g / 10 min. It is a coalescence. S. O. E L606 (manufactured by Asahi Kasei Chemicals Corporation) is a hydrogenated styrene / butadiene block copolymer having a melt flow rate (230 ° C., 2.16 kgf) measured according to ISO 1133 of 2.9 g / 10 min. is there. Tuftec H1052 (manufactured by Asahi Kasei Chemicals Corporation) is a styrene / ethylene / butylene / styrene block copolymer having a melt flow rate (230 ° C., 2.16 kgf) measured in accordance with ISO 1133 of 13.0 g / 10 min. It is a coalescence.

[Example 1]
90 parts by weight of cyclic olefin-based resin and 10 parts by weight of Tuftec H1051 as styrene-based elastomer, with a T-die attached to the tip (specifications: 25 mm diameter, length: 26D, T-die width) : 160 mm) at a predetermined temperature in the temperature range of 210 ° C. to 300 ° C., the cyclic olefin resin composition is extruded at a speed of 250 g / min, and a film having a thickness of 80 μm is wound around a roll. It was.

As shown in Table 2, the short axis dispersion diameter of the styrene elastomer was 0.7 μm. The tear strength was 73 N / mm, which was evaluated as “good”. The initial haze was 2.4%, and the increase in haze after environmental preservation was 0.8%, which was evaluated as ◎.

[Example 2]
90 parts by mass of a cyclic olefin-based resin and S.I. O. A film was produced in the same manner as in Example 1 except that 10 parts by mass of ES1605 was blended and kneaded at a predetermined temperature in the temperature range of 210 ° C. to 300 ° C. using a twin screw extruder.

As shown in Table 2, the short axis dispersion diameter of the styrene elastomer was 2.0 μm. Moreover, tearing strength was evaluation of (circle) in 90 N / mm. The initial haze was 2.9%, and the increase in haze after environmental preservation was 1.4%, which was evaluated as ◯.

[Example 3]
Example 1 except that 90 parts by mass of a cyclic olefin resin and 10 parts by mass of Tuftec H1221 as a styrene elastomer were blended and kneaded at a predetermined temperature in the temperature range of 210 ° C. to 300 ° C. using a twin screw extruder. A film was prepared in the same manner as described above.

As shown in Table 2, the short axis dispersion diameter of the styrene elastomer was 0.9 μm. Moreover, tearing strength was evaluation of (circle) in 78 N / mm. The initial haze was 8.2%, and the increase in haze after environmental preservation was 0.9%, which was evaluated as ◎.

[Example 4]
90 parts by mass of a cyclic olefin-based resin and S.I. O. A film was produced in the same manner as in Example 1 except that 10 parts by mass of E L606 was blended and kneaded at a predetermined temperature in the temperature range of 210 ° C. to 300 ° C. using a twin screw extruder.

As shown in Table 2, the short axis dispersion diameter of the styrene elastomer was 0.1 μm. The tear strength was 102 N / mm, which was a good evaluation. Further, the initial haze was 0.4%, and the increase in haze after environmental preservation was 1.1%, which was evaluated as ◯.

[Example 5]
Example 1 except that 90 parts by mass of a cyclic olefin resin and 10 parts by mass of Tuftec H1051 as a styrene elastomer were blended and kneaded at a predetermined temperature in the temperature range of 210 ° C. to 300 ° C. using a twin screw extruder. A film was prepared in the same manner as described above.

As shown in Table 2, the short axis dispersion diameter of the styrene elastomer was 2.0 μm. Moreover, tearing strength was evaluation of (circle) in 82 N / mm. Further, the initial haze was 3.5%, and the increase in haze after environmental preservation was 1.9%, which was evaluated as ◯.

[Example 6]
Example 1 except that 95 parts by mass of a cyclic olefin resin and 5 parts by mass of Tuftec H1051 as a styrene elastomer were blended and kneaded at a predetermined temperature in the temperature range of 210 ° C. to 300 ° C. using a twin screw extruder. A film was prepared in the same manner as described above.

As shown in Table 2, the short axis dispersion diameter of the styrene elastomer was 0.2 μm. Moreover, tearing strength was evaluation of (circle) in 60 N / mm. The initial haze was 1.3%, and the increase in haze after environmental preservation was 0.5%, which was evaluated as ◎.

[Example 7]
Example 1 except that 65 parts by mass of a cyclic olefin resin and 35 parts by mass of Tuftec H1051 as a styrene elastomer were blended and kneaded at a predetermined temperature in the temperature range of 210 ° C. to 300 ° C. using a twin screw extruder. A film was prepared in the same manner as described above.

As shown in Table 2, the short axis dispersion diameter of the styrene elastomer was 0.4 μm. Moreover, tearing strength was evaluation of (circle) in 120 N / mm. The initial haze was 8.1%, and the increase in haze after environmental preservation was 1.9%, which was evaluated as ◎.

[Comparative Example 1]
A film was prepared in the same manner as in Example 1 except that 100 parts by mass of the cyclic olefin resin without blending with the styrene elastomer was kneaded at a predetermined temperature in the temperature range of 210 ° C. to 300 ° C. using a twin screw extruder. Produced.

As shown in Table 2, the tear strength was 57 N / mm and was evaluated as x. The initial haze was 0.3%, and the increase in haze after environmental preservation was 0.3%, which was evaluated as ◎.

[Comparative Example 2]
Example 1 except that 90 parts by mass of a cyclic olefin resin and 10 parts by mass of Tuftec H1051 as a styrene elastomer were blended and kneaded at a predetermined temperature in the temperature range of 210 ° C. to 300 ° C. using a twin screw extruder. A film was prepared in the same manner as described above.

As shown in Table 2, the short axis dispersion diameter of the styrene elastomer was 2.2 μm. Further, the tear strength was 79 N / mm, which was a good evaluation. The initial haze was 4.2%, and the increase in haze after environmental preservation was 2.7%, which was evaluated as x.

[Comparative Example 3]
Example 1 except that 97 parts by mass of a cyclic olefin resin and 3 parts by mass of Tuftec H1051 as a styrene elastomer were blended and kneaded at a predetermined temperature in the temperature range of 210 ° C. to 300 ° C. using a twin screw extruder. A film was prepared in the same manner as described above.

As shown in Table 2, the short axis dispersion diameter of the styrene elastomer was 0.4 μm. The tear strength was 57 N / mm and was evaluated as x. The initial haze was 1.0%, and the increase in haze after environmental preservation was 0.5%, which was evaluated as ◎.

[Comparative Example 4]
Example 1 except that 60 parts by mass of a cyclic olefin resin and 40 parts by mass of Tuftec H1051 as a styrene elastomer were blended and kneaded at a predetermined temperature in the temperature range of 210 ° C. to 300 ° C. using a twin screw extruder. A film was prepared in the same manner as described above.

As shown in Table 2, the short axis dispersion diameter of the styrene elastomer was 1.2 μm. Moreover, tearing strength was evaluation of (circle) in 131 N / mm. The initial haze was 9.9%, and the increase in haze after environmental preservation was 2.8%, which was evaluated as x.

[Comparative Example 5]
Example 1 except that 90 parts by mass of a cyclic olefin resin and 10 parts by mass of Tuftec H1517 as a styrene elastomer were blended and kneaded at a predetermined temperature in the temperature range of 210 ° C. to 300 ° C. using a twin screw extruder. A film was prepared in the same manner as described above.

As shown in Table 2, the short axis dispersion diameter of the styrene elastomer was 1.8 μm. Moreover, tearing strength was evaluation of (circle) in 62 N / mm. The initial haze was 1.4%, and the increase in haze after environmental preservation was evaluated as x at 2.2%.

[Comparative Example 6]
Example 1 except that 90 parts by mass of a cyclic olefin resin and 10 parts by mass of Tuftec H1052 as a styrene elastomer were blended and kneaded at a predetermined temperature in the temperature range of 210 ° C. to 300 ° C. using a twin screw extruder. A film was prepared in the same manner as described above.

As shown in Table 2, the short axis dispersion diameter of the styrene elastomer was 0.5 μm. Further, the tear strength was 77 N / mm, which was evaluated as o. The initial haze was 10.1%, and the increase in haze after environmental preservation was evaluated as x at 2.5%.

In Comparative Example 1 in which no styrene-based elastomer was added and Comparative Example 3 in which the addition amount was small, the tear strength was less than 60 N / mm and it was easy to break. Moreover, about the comparative example 2 with a large dispersion diameter, and the comparative example 4 with many addition amounts, the haze raise after environmental preservation was larger than 2%. Also in Comparative Examples 5 and 6 in which the MFR of the styrene elastomer was 5.0 g / 10 min or more, the increase in haze after environmental preservation was larger than 2%.

On the other hand, as in Examples 1 to 7, a cyclic olefin resin in which 5-35 wt% of a styrene elastomer having an MFR of 4.5 g / 10 min or less was added and the minor axis dispersion diameter of the styrene elastomer was 2 μm or less. The composition films had good haze increases after environmental preservation of 2% or less and all tear strengths of 60 N / mm or more.

Further, as can be seen from Example 1, Example 5 and Comparative Example 2, the smaller the short axis dispersion diameter of the styrene elastomer, the smaller the haze increase after environmental preservation, and the short axis dispersion diameter is 1 μm or less. No. 1 was particularly good with a haze increase of less than 1%. Further, as can be seen from Example 2 and Example 5, Example 2 having an MFR of 1.0 g / 10 min or more was particularly good with a haze increase of less than 1.5%.

Also, Example 2 and Example 4 in which the styrene elastomer is a hydrogenated styrene / butadiene block copolymer are different from the other examples in which the styrene elastomer is a styrene / ethylene / butylene / styrene block copolymer. It was found that the tear strength tends to be high.

11 Cyclic Olefin Tree, 12 Styrene Elastomer, 21 Dies, 22 Rolls, 23 Resin Material, 31 Retardation Film, 32 Hard Coat Layer, 33 Transparent Conductive Layer, 34 Moth Eye Shaped Structure, 40 Touch Panel, 41 First Transparent conductive film, 42 2nd transparent conductive film, 43 bonding layer, 44 display device, 45 bonding portion, 46 glass substrate, 47 bonding layer, 48 polarizer, 49 front panel, 50 bonding layer, 51 bonding layers, 100 television device, 101 display unit, 110 digital camera, 111 light emitting unit, 112 display unit, 113 menu switch, 114 shutter button, 120 notebook personal computer, 121 main unit, 122 keyboard, 1 3 display unit, 130 a video camera, 131 main body, 132 lens, 133 a start / stop switch, 134 display unit, 140 mobile phones, 141 display unit, 150 a tablet computer, 151 display unit

Claims

A cyclic olefin resin;
In accordance with ISO 1133, a melt flow rate measured under the conditions of 230 ° C. and 2.16 kgf contains a styrene elastomer that is 4.5 g / 10 min or less,
The styrene elastomer is dispersed in the cyclic olefin resin by 5 to 35 wt%,
A cyclic olefin resin composition film in which the short axis dispersion diameter of the styrene elastomer is 2 μm or less.
The cyclic olefin resin composition film according to claim 1, wherein the styrene elastomer has a short axis dispersion diameter of 1 μm or less.
The cyclic olefin resin composition film according to claim 1 or 2, wherein the melt flow rate of the styrene elastomer is 1.0 g / 10 min or more.
The cyclic olefin resin composition film according to claim 1 or 2, wherein the cyclic olefin resin is an addition copolymer of ethylene and norbornene.
The cyclic olefin resin composition film according to claim 3, wherein the cyclic olefin resin is an addition copolymer of ethylene and norbornene.
The styrene elastomer is at least one selected from the group consisting of styrene / ethylene / butylene / styrene block copolymers, styrene / ethylene / propylene / styrene block copolymers, and hydrogenated styrene / butadiene block copolymers. The cyclic olefin resin composition film according to claim 1 or 2.
The styrene elastomer is at least one selected from the group consisting of styrene / ethylene / butylene / styrene block copolymers, styrene / ethylene / propylene / styrene block copolymers, and hydrogenated styrene / butadiene block copolymers. The cyclic olefin resin composition film according to claim 3.
The styrene elastomer is at least one selected from the group consisting of styrene / ethylene / butylene / styrene block copolymers, styrene / ethylene / propylene / styrene block copolymers, and hydrogenated styrene / butadiene block copolymers. The cyclic olefin resin composition film according to claim 4.
The cyclic olefin-based resin composition film according to claim 1 or 2, wherein the styrene-based elastomer is a hydrogenated styrene / butadiene block copolymer.
The cyclic olefin resin composition film according to claim 3, wherein the styrene elastomer is a hydrogenated styrene / butadiene block copolymer.
The cyclic olefin-based resin composition film according to claim 4, wherein the styrene-based elastomer is a hydrogenated styrene / butadiene block copolymer.
The cyclic olefin resin composition film according to claim 5, wherein the styrene elastomer is a hydrogenated styrene / butadiene block copolymer.
A transparent conductive element comprising the cyclic olefin-based resin composition film according to any one of claims 1 to 12 as a base material.
An input device comprising the cyclic olefin-based resin composition film according to any one of claims 1 to 12.
A display device comprising the cyclic olefin-based resin composition film according to any one of claims 1 to 12.
An electronic device comprising the cyclic olefin-based resin composition film according to any one of claims 1 to 12.
A temperature in the range of 210 ° C. to 300 ° C. between a cyclic olefin resin and a styrene elastomer having a melt flow rate measured under conditions of 230 ° C. and 2.16 kgf in accordance with ISO 1133 of 4.5 g / 10 min or less. Melted in
The molten cyclic olefin resin composition is extruded into a film by an extrusion method, and the styrene elastomer is dispersed in the cyclic olefin resin in an amount of 5 to 35 wt%. The manufacturing method of the cyclic olefin resin composition film which obtains the cyclic olefin resin composition film which is 2 micrometers or less.