WO2021070425A1 - Method for manufacturing film laminate having print layer - Google Patents

Method for manufacturing film laminate having print layer Download PDF

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Publication number
WO2021070425A1
WO2021070425A1 PCT/JP2020/024374 JP2020024374W WO2021070425A1 WO 2021070425 A1 WO2021070425 A1 WO 2021070425A1 JP 2020024374 W JP2020024374 W JP 2020024374W WO 2021070425 A1 WO2021070425 A1 WO 2021070425A1
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WO
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Prior art keywords
film
layer
laminate
print layer
hard coat
Prior art date
Application number
PCT/JP2020/024374
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French (fr)
Japanese (ja)
Inventor
岳仁 淵田
康隆 石原
Original Assignee
日東電工株式会社
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Publication date
Application filed by 日東電工株式会社 filed Critical 日東電工株式会社
Priority to KR1020207032487A priority Critical patent/KR20220070380A/en
Priority to CN202080003442.5A priority patent/CN112955320A/en
Publication of WO2021070425A1 publication Critical patent/WO2021070425A1/en

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    • B32B37/00Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding
    • B32B37/02Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding characterised by a sequence of laminating steps, e.g. by adding new layers at consecutive laminating stations
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00Layered products comprising a layer of synthetic resin
    • BPERFORMING OPERATIONS; TRANSPORTING
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    • B32B27/00Layered products comprising a layer of synthetic resin
    • B32B27/18Layered products comprising a layer of synthetic resin characterised by the use of special additives
    • BPERFORMING OPERATIONS; TRANSPORTING
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    • B32B27/00Layered products comprising a layer of synthetic resin
    • B32B27/28Layered products comprising a layer of synthetic resin comprising synthetic resins not wholly covered by any one of the sub-groups B32B27/30 - B32B27/42
    • B32B27/281Layered products comprising a layer of synthetic resin comprising synthetic resins not wholly covered by any one of the sub-groups B32B27/30 - B32B27/42 comprising polyimides
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    • B32B27/30Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers
    • B32B27/302Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers comprising aromatic vinyl (co)polymers, e.g. styrenic (co)polymers
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    • B32B38/0036Heat treatment
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    • B32B7/02Physical, chemical or physicochemical properties
    • B32B7/027Thermal properties
    • B32B7/028Heat-shrinkability
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    • B32B7/04Interconnection of layers
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    • BPERFORMING OPERATIONS; TRANSPORTING
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    • B32B7/04Interconnection of layers
    • B32B7/12Interconnection of layers using interposed adhesives or interposed materials with bonding properties
    • GPHYSICS
    • G02OPTICS
    • G02BOPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B1/00Optical elements characterised by the material of which they are made; Optical coatings for optical elements
    • G02B1/10Optical coatings produced by application to, or surface treatment of, optical elements
    • GPHYSICS
    • G02OPTICS
    • G02BOPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B1/00Optical elements characterised by the material of which they are made; Optical coatings for optical elements
    • G02B1/10Optical coatings produced by application to, or surface treatment of, optical elements
    • G02B1/14Protective coatings, e.g. hard coatings
    • GPHYSICS
    • G09EDUCATION; CRYPTOGRAPHY; DISPLAY; ADVERTISING; SEALS
    • G09FDISPLAYING; ADVERTISING; SIGNS; LABELS OR NAME-PLATES; SEALS
    • G09F9/00Indicating arrangements for variable information in which the information is built-up on a support by selection or combination of individual elements
    • G09F9/30Indicating arrangements for variable information in which the information is built-up on a support by selection or combination of individual elements in which the desired character or characters are formed by combining individual elements
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    • B32B2038/0052Other operations not otherwise provided for
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    • B32B2255/00Coating on the layer surface
    • B32B2255/10Coating on the layer surface on synthetic resin layer or on natural or synthetic rubber layer
    • BPERFORMING OPERATIONS; TRANSPORTING
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    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
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    • B32B2307/00Properties of the layers or laminate
    • B32B2307/50Properties of the layers or laminate having particular mechanical properties
    • B32B2307/536Hardness
    • BPERFORMING OPERATIONS; TRANSPORTING
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    • B32B2457/00Electrical equipment
    • B32B2457/20Displays, e.g. liquid crystal displays, plasma displays

Definitions

  • the present invention relates to a method for producing a film laminate with a print layer.
  • a decorative film (film with a printing layer) is used as a means of improving the design of various products.
  • the portion corresponding to the non-display area of the front plate typically, the peripheral portion.
  • Is provided with a colored layer, a design layer, a decorative layer, or the like for example, Patent Documents 1 and 2).
  • Patent Documents 1 and 2 for example, Patent Documents 1 and 2.
  • the present invention has been made to solve the above-mentioned conventional problems, and an object of the present invention is a simple method for producing a film laminate with a print layer having high pencil hardness and suppressed curling. Is to provide.
  • the method for producing a film laminate with a print layer of the present invention is to form a hard coat layer on one surface of a base film; to form a print layer on the other side of the base film; the hard coat layer.
  • a protective film having a heat shrinkage rate of 0.1% or less in the transport direction is laminated on the surface of the printing layer; and the printed layer is heat-dried with the protective film laminated.
  • the printing layer is heat-dried at 40 ° C. or higher for 20 minutes or longer.
  • the protective film is laminated by roll-to-roll on the surface of the hard coat layer of the laminate of the base film and the hard coat layer.
  • the print layer is formed after laminating the protective film.
  • a laminate of the base film, the hard coat layer, and the protective film is formed into a predetermined size and a predetermined size between the lamination of the protective film and the formation of the printing layer. It further includes cutting into shapes.
  • the hard coat layer is coated with a coating liquid for forming a hard coat layer containing an active energy ray-curable (meth) acrylate to form a coating layer, and the coating layer is irradiated with active energy rays. It is formed by curing it.
  • a method for manufacturing an optical laminate is provided.
  • This manufacturing method includes laminating an optical film on the opposite side of the base film of the film laminate with a printing layer obtained by the above manufacturing method to the hard coat layer. In one embodiment, the manufacturing method comprises laminating the optical films and then peeling off the protective film.
  • a method of manufacturing an image display device includes laminating an optical film and a film laminate with a print layer obtained by the above manufacturing method on the visual side of an image display cell. In one embodiment, the manufacturing method comprises laminating the optical film and the film laminate with a print layer and then peeling off the protective film.
  • Yet another image display device of the present invention includes laminating an optical laminate obtained by the above manufacturing method on the visual side of an image display cell. In one embodiment, the manufacturing method comprises laminating the optical laminate and then peeling off the protective film.
  • a high pencil is obtained by heating and drying the print layer in a state where a protective film having a heat shrinkage ratio of a predetermined value or less is laminated in a predetermined direction.
  • a film laminate with a print layer having hardness and suppressed curl can be easily produced.
  • the protective film is peeled off after the optical film is laminated on the side opposite to the hard coat layer of the base film in the film laminate with the print layer, so that the base film is curled. It can be reliably laminated on the optical film without any problems.
  • FIG. 5 is a schematic cross-sectional view of an optical laminate including the film laminate with a print layer of FIG.
  • A. Method for Producing Film Laminate with Print Layer is to form a hard coat layer on one surface of the base film; the other surface of the base film.
  • a printing layer is formed on the surface of the hard coat layer; a protective film having a heat shrinkage rate of 0.1% or less in the transport direction is laminated on the surface of the hard coat layer; To heat dry;
  • FIG. 1 is a schematic cross-sectional view of a film laminate with a print layer obtained by the production method of the embodiment of the present invention.
  • the film laminate 100 with a print layer of the illustrated example includes a base film 10, a hard coat layer 20 formed on one surface of the base film 10, and a print layer formed on the other side of the base film 10. It has 30 and a protective film 40 laminated on the surface of the hard coat layer 20.
  • the protective film 40 includes a base film (resin film) and an adhesive layer.
  • the protective film 40 is releasably laminated on the surface of the hard coat layer 20 via the pressure-sensitive adhesive layer. If necessary, a hue adjusting layer (not shown) may be provided between the base film 10 and the printing layer 30. Practically, another protective film (sometimes referred to as a process protective film, not shown) may be temporarily attached to the surfaces of the print layer 30 and the base film 10 so as to be peelable.
  • the base film 10 can be made of any suitable material.
  • the constituent materials include polyethylene terephthalate resin, polyethylene naphthalate resin, acetate resin, polyether sulfone resin, polycarbonate resin, polyamide resin, polyimide resin, polyamideimide resin, and polyolefin resin.
  • examples thereof include (meth) acrylic resins, polyvinyl chloride resins, polyvinylidene chloride resins, polystyrene resins, polyvinyl alcohol resins, polyarylate resins, polyphenylene sulfide resins and the like. These resins may be used alone or in combination of two or more.
  • it is a polyamide-based resin, a polyimide-based resin, a polyamide-imide-based resin, a polyethylene naphthalate-based resin, or a polycarbonate-based resin. This is because it has excellent durability and mechanical strength. More preferably, it is a polyimide resin.
  • the base film may contain fine particles blended in the above constituent materials. More specifically, the base film may be a so-called nanocomposite film in which nanometer-order fine particles are dispersed in the matrix of the constituent materials. With such a configuration, very good hardness and scratch resistance can be imparted.
  • the average particle size of the fine particles is, for example, about 1 nm to 100 nm.
  • the fine particles are typically composed of inorganic oxides.
  • the surface of the fine particles is modified with a predetermined functional group.
  • Examples of the inorganic oxides constituting the fine particles include zirconium oxide, ittoria-added zirconium oxide, lead zirconate, strontium titanate, tin titanate, tin oxide, bismuth oxide, niobium oxide, tantalum oxide, potassium tantalate, and tungsten oxide. , Cerium oxide, lanthanum oxide, gallium oxide and the like, silica, alumina, titanium oxide, zirconium oxide, barium titanate and the like.
  • the thickness of the base film is preferably 40 ⁇ m to 100 ⁇ m, more preferably 50 ⁇ m to 80 ⁇ m. With such a thickness, the balance between thinning, handleability, and mechanical strength is excellent.
  • the pencil hardness of the base film is preferably B or higher, more preferably F or higher, and even more preferably H or higher.
  • the hard coat layer 20 is typically coated with a coating liquid for forming a hard coat layer to form a coating layer, and the coating layer is irradiated with active energy rays (for example, ultraviolet rays) to be cured. Is formed by The coating liquid for forming a hard coat layer contains an active energy ray-curable (meth) acrylate as a base resin.
  • active energy ray-curable (meth) acrylate examples include an ultraviolet curable (meth) acrylate and an electron beam-curable (meth) acrylate.
  • a UV curable (meth) acrylate is preferred. This is because the hard coat layer can be efficiently formed by a simple processing operation.
  • the UV curable (meth) acrylate contains UV curable monomers, oligomers, polymers and the like.
  • the UV curable (meth) acrylate contains a monomer component and an oligomer component having preferably 2 or more, more preferably 3 to 6 UV polymerization functional groups.
  • the ultraviolet curable (meth) acrylate contains a photopolymerization initiator.
  • the curing method may be a radical polymerization method or a cationic polymerization method.
  • an organic-inorganic hybrid material in which silica particles, a polysilsesquioxane compound, or the like is mixed with (meth) acrylate may be used.
  • (meth) acrylate means acrylate and / or methacrylate.
  • a slide ring material may be blended with the ultraviolet curable (meth) acrylate. Good flexibility can be imparted by blending the slide ring material.
  • Polyrotaxane is a typical example of the slide ring material. Polyrotaxane typically has a structure in which a cyclodextrin (CD) cyclic molecule slides on a linear polyethylene glycol (PEG) main chain. Both ends of the PEG backbone are modified with adamantaneamine to prevent shedding of the CD cyclic molecule. In polyrotaxane, preferably, the CD cyclic molecule is chemically modified to impart an active energy ray-polymerizable group.
  • a radically polymerizable monomer having a radically polymerizable group is preferably used as the ultraviolet curable (meth) acrylate.
  • the radically polymerizable group include a (meth) acryloyl group and a (meth) acryloyloxy group. This is because it has excellent compatibility with polyrotaxane and various material selections are possible.
  • polyrotaxane substantially a polymerizable group of a CD cyclic molecule
  • the ultraviolet curable (meth) acrylate may contain nanofibers and / or nanocrystals.
  • Typical examples of nanofibers include cellulose nanofibers, chitin nanofibers, and chitosan nanofibers. By blending these, a hard coat layer having excellent flexibility, pencil hardness, scratch resistance, and abrasion resistance can be obtained while maintaining excellent transparency.
  • the nanofibers and / or nanocrystals (the total when used in combination) can be blended in a proportion of 0.1% to 40% by weight, preferably 0.1% by weight, based on the entire hard coat layer.
  • Nanofibers have an average fiber diameter of, for example, 1 nm to 100 nm, and an average fiber length of, for example, 10 nm to 1000 nm.
  • the hard coat layer containing nanofibers is described in, for example, Japanese Patent Application Laid-Open No. 2012-131201 and Japanese Patent Application Laid-Open No. 2012-171171. The description of this publication is incorporated herein by reference.
  • the coating liquid may further contain any suitable additive depending on the purpose.
  • Additives include, for example, photopolymerization initiators, leveling agents, blocking inhibitors, dispersion stabilizers, rockers, antioxidants, UV absorbers, defoamers, thickeners, dispersants, surfactants, etc. Examples thereof include catalysts, fillers, lubricants, and antistatic agents.
  • the type, combination, content, etc. of the additives contained can be appropriately set according to the purpose and desired characteristics.
  • Active energy ray (e.g., ultraviolet) irradiation amount is, for example, 150mJ / cm 2 ⁇ 400mJ / cm 2.
  • the coating layer may be heated before irradiation with active energy rays.
  • the heating temperature is, for example, 70 ° C to 100 ° C.
  • the heating time is, for example, 1 minute to 4 minutes.
  • the thickness of the formed hard coat layer is preferably 3 ⁇ m to 20 ⁇ m, and more preferably 3 ⁇ m to 15 ⁇ m. When the thickness is in such a range, curling can be satisfactorily suppressed, and both excellent surface hardness and flexibility and / or foldability can be achieved at the same time.
  • the protective film 40 can be typically laminated by roll-to-roll on the surface of the hard coat layer of the laminate of the base film / hard coat layer.
  • the larger of the heat shrinkage rate in the first direction and the heat shrinkage rate in the second direction orthogonal to the first direction of the protective film is 0.1% or less, preferably 0.08%. It is less than or equal to, more preferably 0.06% or less, still more preferably 0.05% or less.
  • the lower limit of the heat shrinkage rate can be, for example, 0.01%. When the heat shrinkage rate is within such a range, curl of the film laminate with a print layer (particularly, curl due to heating at the time of forming the print layer) can be remarkably suppressed.
  • the first direction is typically the transport direction of the protective film.
  • the heat shrinkage rate in the transport direction is larger than the heat shrinkage rate in the direction orthogonal to the transport direction (width direction).
  • Such properties regarding the coefficient of thermal shrinkage in the protective film can be realized by lowering the glass transition temperature or increasing the coefficient of linear expansion.
  • the protective film can be made of any suitable material that can achieve the heat shrinkage as described above.
  • the constituent materials include polyester resins such as polyethylene terephthalate, cycloolefin resins such as norbornene resins, polyamide resins, polycarbonate resins, and copolymer resins thereof.
  • a polyester resin is preferable, and polyethylene terephthalate is more preferable.
  • the thickness of the protective film is preferably 30 ⁇ m to 140 ⁇ m, preferably 35 ⁇ m to 135 ⁇ m. With such a thickness, curling of the film laminate with a print layer can be remarkably suppressed due to a synergistic effect with the above-mentioned characteristics related to the heat shrinkage rate.
  • the protective film includes the base film (resin film) and the pressure-sensitive adhesive layer, and the thickness of the protective film is the total thickness of the base film and the pressure-sensitive adhesive layer.
  • the elastic modulus of the protective film is preferably 2.2 kN / mm 2 to 4.8 kN / mm 2 .
  • the elastic modulus is measured according to JIS K 6781.
  • the tensile elongation of the protective film is preferably 90% to 170%.
  • the tensile elongation is measured in accordance with JIS K6781.
  • the print layer 30 can typically be formed after laminating the protective film. More specifically, the print layer may be formed after the laminate of the base film / hard coat layer / protective film is cut into a predetermined size and shape. Regarding cutting, for example, when the laminated body is cut into a rectangular shape, the laminated body may be cut into a rectangular shape so that the long side direction (transportation direction) of the laminated body is the long side direction, or the rectangular body is cut into a rectangular shape so as to be the short side direction. You may cut it into.
  • the print layer can be formed by any suitable printing method using any suitable ink or paint.
  • Specific examples of the printing method include gravure printing, offset printing, silk screen printing, and transfer printing from a transfer sheet.
  • the ink or paint used typically includes a binder, a colorant, a solvent and any suitable additive that may be used as needed.
  • the binder include chlorinated polyolefins (for example, chlorinated polyethylene and chlorinated polypropylene), polyester resins, urethane resins, acrylic resins, vinyl acetate resins, vinyl chloride-vinyl acetate copolymers, and cellulose resins. ..
  • the binder resin may be used alone or in combination of two or more.
  • the binder resin is a thermosetting resin. Since the thermosetting resin can be used in a smaller amount than the photopolymerizable resin, the amount of the colorant used (colorant content in the colored layer) can be increased.
  • the binder resin is a (meth) acrylic resin, preferably a (meth) acrylic resin containing a polyfunctional monomer (eg, pentaerythritol tri (meth) acrylate) as a copolymerization component.
  • a polyfunctional monomer eg, pentaerythritol tri (meth) acrylate
  • a printed layer having an appropriate elastic modulus can be formed.
  • a step is also formed due to the thickness of the print layer, and the step can effectively function to prevent blocking.
  • any suitable colorant can be used depending on the purpose and the desired color.
  • colorants include inorganic pigments such as titanium white, zinc flower, carbon black, iron black, valve handle, chrome vermilion, ultramarine blue, cobalt blue, yellow lead, and titanium yellow; phthalocyanine blue, induslen blue, and iso.
  • Organic pigments or dyes such as indolinone yellow, benzidine yellow, quinacridone red, polyazo red, perylene red, aniline black; metal pigments composed of scaly foil pieces such as aluminum and brass; scales such as titanium dioxide coated mica and basic lead carbonate. Examples thereof include pearl luster pigments (pearl pigments) composed of shaped foil pieces.
  • a black colored layer carbon black, iron black, and aniline black are preferably used.
  • a colorant in combination. This is because it can absorb visible light over a wide range and evenly to form a non-colored (ie, black) colored layer.
  • azo compounds and / or quinone compounds can be used.
  • the colorant comprises carbon black as a main component and other colorants (eg, azo compounds and / or quinone compounds). According to such a configuration, it is possible to form a colored layer that is not colored and has excellent stability over time.
  • the colorant When forming a black colored layer, the colorant can be used in a ratio of preferably 50 parts by weight to 200 parts by weight with respect to 100 parts by weight of the binder resin.
  • the content ratio of carbon black in the colorant is preferably 80% to 100%.
  • the printed layer formed is a colored layer that is colored by printing according to the application and the desired design. Examples of the color of the print layer include black, brown, white, dark blue, red, gold, and silver.
  • the printing layer may be a design layer having a predetermined design, or may be a solid colored layer.
  • the printing layer is preferably a solid colored layer, and more preferably a black colored layer.
  • wiring, terminals, a backlight, and other parts can be concealed in a non-display area. That is, the print layer can function as a concealment layer.
  • the print layer can be formed in any suitable pattern depending on the purpose. In one embodiment, the print layer may be formed in a position corresponding to the bezel.
  • the non-display area can be concealed without using a bezel, so that an image display device that does not use a bezel can be realized.
  • an image display device having an extremely excellent appearance with no step on the outermost surface.
  • the thickness of the printed layer formed is preferably 3 ⁇ m to 15 ⁇ m. Further, the printed layer has a total light transmittance of preferably 0.01% or less, more preferably 0.008% or less at a thickness of 3 ⁇ m to 15 ⁇ m. When the total light transmittance is in such a range, the non-display area of the image display device can be well concealed without using the bezel.
  • the final film laminate with the print layer can be obtained. That is, the heat-drying of the print layer is performed in a state where the protective films are laminated. Curling can be remarkably suppressed by heating and drying the print layer in a state where the protective films are laminated. Heat drying is typically performed at 40 ° C. or higher for 20 minutes or longer.
  • the heating temperature is preferably 50 ° C. or higher, more preferably 60 ° C. or higher, and even more preferably 70 ° C. or higher.
  • the upper limit of the heating temperature can be, for example, 95 ° C.
  • the heating time is preferably 30 minutes or more, more preferably 40 minutes or more, still more preferably 50 minutes or more, and particularly preferably 60 minutes or more.
  • the upper limit of the heating time can be, for example, 90 minutes. If the heating temperature is too high and / or the heating time is too long, the curl of the film laminate with the print layer becomes large, and / or the film laminate with the print layer softens or melts due to heat and breaks. There is. If the heating temperature is too low and / or the heating time is too short, the print layer may not be sufficiently formed.
  • a process protection film is temporarily attached to the print layer and the surface of the base film of the obtained film laminate with a print layer so as to be peelable.
  • the film laminate with a print layer to which the process protection film is temporarily attached is used for alignment cutting, pre-shipment inspection, and the like.
  • the protective film and the process protective film are peeled off and removed.
  • the protective film is stripped off (substantially at the end) after the process protective film.
  • the film laminate with print layer has a warp amount of 19 mm or less, preferably 15 mm or less, more preferably 10 mm or less after being placed in an environment of 70 ° C. for 60 minutes. It is more preferably 7 mm or less.
  • the lower limit of the amount of warpage can be, for example, 2 mm.
  • the amount of warpage (curl) can be made very small in the film laminate with a print layer. As a result, the film laminate with the print layer can be reliably and satisfactorily laminated on the optical film or the image display cell.
  • the visible side surface (substantially the surface of the hard coat layer) of the film laminate with the printing layer has a pencil hardness of preferably 2H or more, more preferably 3H or more, still more preferably 4H or more.
  • the film laminate with a print layer can function well as a window film.
  • Pencil hardness can be measured according to JIS K 5400-5-4.
  • the visible surface has scratch resistance that does not cause scratches even if it is rubbed back and forth preferably 300 times, more preferably 500 times, and even more preferably 1000 times under a load of 1000 g.
  • the scratch resistance can be evaluated in the state of scratches when steel wool # 0000 is used and the surface is reciprocated a predetermined number of times under a predetermined load (for example, 500 g / cm 2 , 1000 g / cm 2).
  • the film laminate with a printing layer has a radius of curvature of 3 mm or less (for example, 3 mm, 2 mm, 1 mm) and has flexibility that allows it to bend preferably 50,000 times, more preferably 100,000 times, and even more preferably 200,000 times. Since the film laminate with a print layer has such flexibility, it is possible to realize an image display device that is bendable or foldable when the film laminate with a print layer is applied to an image display device. The flexibility test is performed by bending with the hard coat layer inside.
  • a film laminate with a print layer is cut out into a strip of 100 mm ⁇ 20 mm and used as a measurement sample, and the test machine (“CL09-typeD01-FMC90” manufactured by Yuasa System Co., Ltd.) is used. Set the measurement sample so that the hard coat layer side is inside the bend, and perform under the following conditions.
  • the evaluation of the flexibility can be judged by visually observing the state of peeling at the bent portion of the sample after the test.
  • Environmental conditions 25 ° C, 55% RH Test speed: 60 rpm
  • the light transmittance of the film laminate with a print layer is preferably 85% or more, more preferably 87% or more, and further preferably 90% or more.
  • the haze of the film laminate with a print layer is preferably 1.5% or less, more preferably 1.2% or less, and further preferably 1.0% or less.
  • the film laminate with a print layer can be suitably used as, for example, a window film of an image display device, a front plate of a car navigation system, and a dust cover of a head-up display system.
  • FIG. 2 is a schematic cross-sectional view of an optical laminate including the film laminate with a print layer of FIG.
  • the optical laminate 200 of the illustrated example has a film laminate 100 with a print layer and an optical film 120.
  • the optical film 120 is arranged on the side opposite to the hard coat layer 20 of the base film 10 in the film laminate 100 with a print layer.
  • the optical film 120 is typically laminated on the film laminate 100 with a print layer via an adhesive layer 140.
  • the adhesive layer is composed of any suitable adhesive or adhesive depending on the purpose.
  • the film laminate 100 with a print layer is as described in item A above.
  • optical film 120 examples include any suitable optical film.
  • the optical film may be a film composed of a single layer or a laminated body.
  • Specific examples of the optical film composed of a single layer include a polarizer and a retardation film.
  • Specific examples of the optical film configured as a laminate include a polarizing plate (typically, a laminate of a polarizing element and a protective film), a conductive film for a touch panel, a surface treatment film, and a single layer thereof.
  • Examples thereof include a laminated body (for example, a circular polarizing plate for antireflection, a polarizing plate with a conductive layer for a touch panel) in which an optical film formed as an optical film and / or an optical film formed as a laminated body is appropriately laminated according to a purpose.
  • a laminated body for example, a circular polarizing plate for antireflection, a polarizing plate with a conductive layer for a touch panel
  • an optical film formed as an optical film and / or an optical film formed as a laminated body is appropriately laminated according to a purpose.
  • the optical laminate 200 can be produced by laminating the optical film 120 on the side opposite to the hard coat layer 20 of the base film 10 in the film laminate 100 with a print layer. After laminating the optical film 120, the protective film 40 is peeled off.
  • the film laminate with a print layer according to item A and the optical laminate according to item B can be applied to an image display device.
  • the image display device include a liquid crystal display device and an electroluminescence (EL) display device (for example, an organic EL display device and an inorganic EL display device).
  • the image display device typically includes a film laminate with a print layer or an optical laminate on the visual side of the image display cell.
  • the image display device is preferably an organic EL display device.
  • the image display device has a curved shape (substantially a curved display screen) and / or is bendable or bendable. More preferably, the image display device is foldable.
  • the image display device can be manufactured by laminating the optical film 120 and the film laminate 100 with a print layer on the visual side of the image display cell (not shown). After laminating the optical film 120 and the film laminate 100 with a print layer, the protective film 40 is peeled off.
  • the image display device can be manufactured by laminating the optical laminate 200 on the visual side of the image display cell (not shown). After laminating the optical laminate 200, the protective film 40 is peeled off.
  • the measurement method of each characteristic is as follows. (1) Thickness Measured with a micro gauge type thickness gauge manufactured by Mitutoyo. The thickness of the base film / hard coat layer laminate was measured, and the thickness of the hard coat layer was calculated by subtracting the thickness of the base film. (2) Heat Shrinkage Rate of Protective Film The protective film used in Examples and Comparative Examples was cut into sizes of 100 mm in the long direction and 100 mm in the width direction to prepare test samples. The initial dimensions of this test sample were measured using an image measuring machine "QVA606-PRO_AE10" manufactured by Mitutoyo. The test sample was then heated at 70 ° C.
  • Example 1 1.
  • coating liquid for forming hard coat layer 100 parts by mass of ultraviolet curable polyfunctional acrylate (manufactured by Aika Kogyo Co., Ltd., product name "Z-850-16") as base resin, leveling agent (manufactured by DIC Co., Ltd., product name: GRANDIC) PC-4100) 5 parts by mass and 3 parts by mass of a photopolymerization initiator (manufactured by Ciba Japan, trade name: Irgacure 907) are mixed and diluted with methylisobutylketone so that the solid content concentration becomes 50% by mass. To prepare a coating liquid for forming a hard coat layer.
  • ultraviolet curable polyfunctional acrylate manufactured by Aika Kogyo Co., Ltd., product name "Z-850-16
  • leveling agent manufactured by DIC Co., Ltd., product name: GRANDIC
  • a photopolymerization initiator manufactured by Ciba Japan, trade name: Irgacure 907
  • the weight average molecular weight of the acrylic polymer (A) was 600,000, and the Tg was ⁇ 50 ° C.
  • Acrylic polymer (A) solution (30% by weight) is diluted to 20% by weight with ethyl acetate, and an epoxy-based cross-linking agent (Mitsubishi Gas) is used as a cross-linking agent for 100 parts by weight (solid content) of the acrylic polymer in this solution.
  • 11 parts by weight of TETRAD-C) manufactured by Kagaku Co., Ltd. was added, and the mixture was mixed and stirred for about 1 minute at about 25 ° C. to prepare an acrylic pressure-sensitive adhesive composition.
  • the acrylic pressure-sensitive adhesive composition is applied to one side of a polyethylene terephthalate (PET) base material (thickness 110 ⁇ m) and heated at 140 ° C. for 60 seconds to form a pressure-sensitive adhesive layer having a thickness of 20 ⁇ m. A thickness of 130 ⁇ m) was produced. The heat shrinkage of the obtained protective film was 0.04%.
  • PET polyethylene terephthalate
  • the protective film obtained in 1) was laminated by roll-to-roll to prepare a film laminate.
  • the obtained film laminate was cut into sizes of 100 mm in the long direction and 100 mm in the width direction, and black ink was printed on the peripheral edge thereof by gravure printing to form a flat printing layer (black colored layer).
  • the width of the print layer was 12 mm and the thickness was 10 ⁇ m. In this way, a film laminate with a print layer was produced.
  • the formulation of the black ink was as follows: 100 parts of binder resin (acrylic resin: manufactured by Kyoeisha Chemical Co., Ltd., trade name: light acrylate PE-3A), 100 parts of carbon black, solvent for adjusting viscosity ( Methyl ethyl ketone: MEK) 200 parts. These mixtures were subjected to a high dispersion treatment by ultrasonic waves to improve diffusivity.
  • binder resin acrylic resin: manufactured by Kyoeisha Chemical Co., Ltd., trade name: light acrylate PE-3A
  • MEK Methyl ethyl ketone
  • the obtained film laminate with a print layer (substantially, the print layer) was dried at 70 ° C. for 60 minutes to obtain a final film laminate with a print layer.
  • the obtained film laminate with a print layer was subjected to the evaluations (3) and (4) above. The results are shown in Table 1.
  • Example 2 A film laminate with a print layer was obtained in the same manner as in Example 1 except that the film was dried at 60 ° C. for 50 minutes. The obtained film laminate with a print layer was subjected to the same evaluation as in Example 1. The results are shown in Table 1.
  • Example 3 A film laminate with a print layer was obtained in the same manner as in Example 1 except that the film was dried at 50 ° C. for 40 minutes. The obtained film laminate with a print layer was subjected to the same evaluation as in Example 1. The results are shown in Table 1.
  • Example 4 A film laminate with a print layer was obtained in the same manner as in Example 1 except that the film was dried at 40 ° C. for 30 minutes. The obtained film laminate with a print layer was subjected to the same evaluation as in Example 1. The results are shown in Table 1.
  • Example 5 A film laminate with a print layer was obtained in the same manner as in Example 1 except that the base film was changed to another transparent polyimide film (manufactured by KOLON, product name “CPITMC_50”, thickness 50 ⁇ m). The obtained film laminate with a print layer was subjected to the same evaluation as in Example 1. The results are shown in Table 1.
  • Example 6> A film laminate with a print layer was obtained in the same manner as in Example 1 except that the thickness of the hard coat layer was 3 ⁇ m. The obtained film laminate with a print layer was subjected to the same evaluation as in Example 1. The results are shown in Table 1.
  • Example 7 A film laminate with a print layer was obtained in the same manner as in Example 1 except that the thickness of the hard coat layer was 8 ⁇ m. The obtained film laminate with a print layer was subjected to the same evaluation as in Example 1. The results are shown in Table 1.
  • Example 8> A film laminate with a print layer was obtained in the same manner as in Example 1 except that the thickness of the hard coat layer was 13 ⁇ m. The obtained film laminate with a print layer was subjected to the same evaluation as in Example 1. The results are shown in Table 1.
  • Example 9 A film laminate with a print layer was obtained in the same manner as in Example 1 except that the thickness of the hard coat layer was 20 ⁇ m. The obtained film laminate with a print layer was subjected to the same evaluation as in Example 1. The results are shown in Table 1.
  • Example 10 A film laminate with a print layer in the same manner as in Example 1 except that the protective film was changed to another polyethylene terephthalate film (manufactured by Nitto Denko Corporation, product name "IP300F", thickness 38 ⁇ m, heat shrinkage rate 0.07%). Got The obtained film laminate with a print layer was subjected to the same evaluation as in Example 1. The results are shown in Table 1.
  • Example 1 A film laminate with a print layer was prepared in the same manner as in Example 1 except that the protective film was changed to a polyethylene film (manufactured by Toray Film Processing Co., Ltd., product name "Tretec 7832C", thickness 30 ⁇ m, heat shrinkage rate 0.87%). Obtained. The obtained film laminate with a print layer was subjected to the same evaluation as in Example 1. The results are shown in Table 1.
  • Example 2 A film laminate with a print layer was prepared in the same manner as in Example 5 except that the protective film was changed to a polyethylene film (manufactured by Toray Film Processing Co., Ltd., product name "Tretec 7832C", thickness 30 ⁇ m, heat shrinkage rate 0.87%). Obtained. The obtained film laminate with a print layer was subjected to the same evaluation as in Example 1. The results are shown in Table 1.
  • the film laminate with a print layer of the present invention can be suitably used as a window film of an image display device.
  • the optical laminate of the present invention can be suitably used as a visible side member of an image display device.
  • Base film 20 Hard coat layer 30 Printing layer 40 Protective film 100 Film laminate with printing layer 120 Optical film 200 Optical laminate

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Abstract

Provided is a simple method for manufacturing a film laminate (100) having a print layer, the film laminate having high pencil hardness and suppressed curling. This method for manufacturing a film laminate having a print layer includes: forming a hard coat layer (20) on one surface of a base material film (10); forming a print layer (30) on another surface of the base material film; laminating a protective film (40) having a heat shrinkage rate in a conveyance direction of 0.1% or less on the surface of the hard coat layer; and heating and drying the print layer while a protective film is laminated thereon.

Description

印刷層付フィルム積層体の製造方法Manufacturing method of film laminate with print layer
 本発明は、印刷層付フィルム積層体の製造方法に関する。 The present invention relates to a method for producing a film laminate with a print layer.
 各種製品のデザイン性向上の手段として、加飾フィルム(印刷層付フィルム)が用いられている。例えば、画像表示装置のデザイン性向上(例えば、非表示領域の配線等のベゼルを用いない隠蔽)の手段の1つとして、前面板の非表示領域に対応する部分(代表的には、周縁部)に着色層、意匠層または装飾層等を設けることが提案されている(例えば、特許文献1および2)。しかし、印刷層を形成するためには長時間加熱乾燥する必要があり、その結果、印刷層付フィルムがカールしてしまうという問題がある。 A decorative film (film with a printing layer) is used as a means of improving the design of various products. For example, as one of the means for improving the design of the image display device (for example, concealing the wiring of the non-display area without using a bezel), the portion corresponding to the non-display area of the front plate (typically, the peripheral portion). ) Is provided with a colored layer, a design layer, a decorative layer, or the like (for example, Patent Documents 1 and 2). However, in order to form the print layer, it is necessary to heat and dry it for a long time, and as a result, there is a problem that the film with the print layer is curled.
特開2011-194799号公報Japanese Unexamined Patent Publication No. 2011-194799 特開2017-126003号公報JP-A-2017-126003
 本発明は上記従来の課題を解決するためになされたものであり、その目的とするところは、高い鉛筆硬度を有し、かつ、カールが抑制された印刷層付フィルム積層体の簡便な製造方法を提供することにある。 The present invention has been made to solve the above-mentioned conventional problems, and an object of the present invention is a simple method for producing a film laminate with a print layer having high pencil hardness and suppressed curling. Is to provide.
 本発明の印刷層付フィルム積層体の製造方法は、基材フィルムの一方の面にハードコート層を形成すること;該基材フィルムの他方の面に印刷層を形成すること;該ハードコート層の表面に、搬送方向の熱収縮率が0.1%以下である保護フィルムを積層すること;および、該保護フィルムを積層した状態で該印刷層を加熱乾燥すること;を含む。
 1つの実施形態においては、上記印刷層の加熱乾燥は、40℃以上で20分以上行われる。
 1つの実施形態においては、上記保護フィルムは、上記基材フィルムと上記ハードコート層との積層体のハードコート層表面にロールトゥロールにより積層される。
 1つの実施形態においては、上記印刷層は、上記保護フィルムの積層後に形成される。
 1つの実施形態においては、上記製造方法は、上記保護フィルムの積層と上記印刷層の形成との間に、上記基材フィルムと上記ハードコート層と該保護フィルムとの積層体を所定サイズおよび所定形状に裁断することをさらに含む。
 1つの実施形態においては、上記ハードコート層は、活性エネルギー線硬化型(メタ)アクリレートを含むハードコート層形成用塗布液を塗布して塗布層を形成し、該塗布層に活性エネルギー線を照射して硬化させることにより形成される。
 本発明の別の局面によれば、光学積層体の製造方法が提供される。この製造方法は、上記の製造方法により得られた印刷層付フィルム積層体の上記基材フィルムの上記ハードコート層と反対側に、光学フィルムを積層することを含む。
 1つの実施形態においては、上記製造方法は、上記光学フィルムを積層した後、上記保護フィルムを剥離することを含む。
 本発明のさらに別の局面によれば、画像表示装置の製造方法が提供される。この製造方法は、画像表示セルの視認側に光学フィルムおよび上記の製造方法により得られた印刷層付フィルム積層体を積層することを含む。
 1つの実施形態においては、上記製造方法は、上記光学フィルムおよび上記印刷層付フィルム積層体を積層した後、上記保護フィルムを剥離することを含む。
 本発明のさらに別の画像表示装置は、画像表示セルの視認側に上記の製造方法により得られた光学積層体を積層することを含む。
 1つの実施形態においては、上記製造方法は、上記光学積層体を積層した後、上記保護フィルムを剥離することを含む。
The method for producing a film laminate with a print layer of the present invention is to form a hard coat layer on one surface of a base film; to form a print layer on the other side of the base film; the hard coat layer. A protective film having a heat shrinkage rate of 0.1% or less in the transport direction is laminated on the surface of the printing layer; and the printed layer is heat-dried with the protective film laminated.
In one embodiment, the printing layer is heat-dried at 40 ° C. or higher for 20 minutes or longer.
In one embodiment, the protective film is laminated by roll-to-roll on the surface of the hard coat layer of the laminate of the base film and the hard coat layer.
In one embodiment, the print layer is formed after laminating the protective film.
In one embodiment, in the manufacturing method, a laminate of the base film, the hard coat layer, and the protective film is formed into a predetermined size and a predetermined size between the lamination of the protective film and the formation of the printing layer. It further includes cutting into shapes.
In one embodiment, the hard coat layer is coated with a coating liquid for forming a hard coat layer containing an active energy ray-curable (meth) acrylate to form a coating layer, and the coating layer is irradiated with active energy rays. It is formed by curing it.
According to another aspect of the present invention, there is provided a method for manufacturing an optical laminate. This manufacturing method includes laminating an optical film on the opposite side of the base film of the film laminate with a printing layer obtained by the above manufacturing method to the hard coat layer.
In one embodiment, the manufacturing method comprises laminating the optical films and then peeling off the protective film.
According to yet another aspect of the present invention, there is provided a method of manufacturing an image display device. This manufacturing method includes laminating an optical film and a film laminate with a print layer obtained by the above manufacturing method on the visual side of an image display cell.
In one embodiment, the manufacturing method comprises laminating the optical film and the film laminate with a print layer and then peeling off the protective film.
Yet another image display device of the present invention includes laminating an optical laminate obtained by the above manufacturing method on the visual side of an image display cell.
In one embodiment, the manufacturing method comprises laminating the optical laminate and then peeling off the protective film.
 本発明の実施形態によれば、印刷層付フィルム積層体の製造方法において、所定方向に所定値以下の熱収縮率を有する保護フィルムを積層した状態で印刷層を加熱乾燥することにより、高い鉛筆硬度を有し、かつ、カールが抑制された印刷層付フィルム積層体を簡便に製造することができる。さらに、本発明の実施形態によれば、印刷層付フィルム積層体における基材フィルムのハードコート層と反対側に光学フィルムを積層した後で保護フィルムを剥離するので、基材フィルムがカールすることなく確実に光学フィルムに積層することができる。 According to the embodiment of the present invention, in the method for producing a film laminate with a print layer, a high pencil is obtained by heating and drying the print layer in a state where a protective film having a heat shrinkage ratio of a predetermined value or less is laminated in a predetermined direction. A film laminate with a print layer having hardness and suppressed curl can be easily produced. Further, according to the embodiment of the present invention, the protective film is peeled off after the optical film is laminated on the side opposite to the hard coat layer of the base film in the film laminate with the print layer, so that the base film is curled. It can be reliably laminated on the optical film without any problems.
本発明の実施形態の製造方法により得られる印刷層付フィルム積層体の概略断面図である。It is the schematic sectional drawing of the film laminated body with a print layer obtained by the manufacturing method of embodiment of this invention. 図1の印刷層付フィルム積層体を含む光学積層体の概略断面図である。FIG. 5 is a schematic cross-sectional view of an optical laminate including the film laminate with a print layer of FIG.
 以下、本発明の代表的な実施形態について説明するが、本発明はこれらの実施形態には限定されない。 Hereinafter, typical embodiments of the present invention will be described, but the present invention is not limited to these embodiments.
A.印刷層付フィルム積層体の製造方法
 本発明の実施形態による印刷層付フィルム積層体の製造方法は、基材フィルムの一方の面にハードコート層を形成すること;該基材フィルムの他方の面に印刷層を形成すること;該ハードコート層の表面に、搬送方向の熱収縮率が0.1%以下である保護フィルムを積層すること;および、該保護フィルムを積層した状態で該印刷層を加熱乾燥すること;を含む。
A. Method for Producing Film Laminate with Print Layer The method for producing a film laminate with print layer according to the embodiment of the present invention is to form a hard coat layer on one surface of the base film; the other surface of the base film. A printing layer is formed on the surface of the hard coat layer; a protective film having a heat shrinkage rate of 0.1% or less in the transport direction is laminated on the surface of the hard coat layer; To heat dry;
A-1.得られる印刷層付フィルム積層体の全体構成
 当該製造方法の理解を容易にするために、最初に、当該製造方法により得られる印刷層付フィルム積層体の全体構成および構成要素を簡単に説明する。図1は、本発明の実施形態の製造方法により得られる印刷層付フィルム積層体の概略断面図である。図示例の印刷層付フィルム積層体100は、基材フィルム10と、基材フィルム10の一方の面に形成されたハードコート層20と、基材フィルム10の他方の面に形成された印刷層30と、ハードコート層20の表面に積層された保護フィルム40と、を有する。保護フィルム40は、ベースフィルム(樹脂フィルム)と粘着剤層とを含む。保護フィルム40は、当該粘着剤層を介してハードコート層20の表面に剥離可能に積層されている。必要に応じて、基材フィルム10と印刷層30との間には、色相調整層(図示せず)が設けられていてもよい。実用的には、印刷層30および基材フィルム10表面に、別の保護フィルム(工程保護フィルムと称される場合がある、図示せず)が剥離可能に仮着されていてもよい。
A-1. Overall configuration of the obtained film laminate with a print layer In order to facilitate understanding of the manufacturing method, first, the overall configuration and components of the film laminate with a print layer obtained by the manufacturing method will be briefly described. FIG. 1 is a schematic cross-sectional view of a film laminate with a print layer obtained by the production method of the embodiment of the present invention. The film laminate 100 with a print layer of the illustrated example includes a base film 10, a hard coat layer 20 formed on one surface of the base film 10, and a print layer formed on the other side of the base film 10. It has 30 and a protective film 40 laminated on the surface of the hard coat layer 20. The protective film 40 includes a base film (resin film) and an adhesive layer. The protective film 40 is releasably laminated on the surface of the hard coat layer 20 via the pressure-sensitive adhesive layer. If necessary, a hue adjusting layer (not shown) may be provided between the base film 10 and the printing layer 30. Practically, another protective film (sometimes referred to as a process protective film, not shown) may be temporarily attached to the surfaces of the print layer 30 and the base film 10 so as to be peelable.
A-2.基材フィルム
 基材フィルム10は、任意の適切な材料で構成され得る。構成材料の具体例としては、ポリエチレンテレフタレート系樹脂、ポリエチレンナフタレート系樹脂、アセテート系樹脂、ポリエーテルスルホン系樹脂、ポリカーボネート系樹脂、ポリアミド系樹脂、ポリイミド系樹脂、ポリアミドイミド系樹脂、ポリオレフィン系樹脂、(メタ)アクリル系樹脂、ポリ塩化ビニル系樹脂、ポリ塩化ビニリデン系樹脂、ポリスチレン系樹脂、ポリビニルアルコール系樹脂、ポリアリレート系樹脂、ポリフェニレンサルファイド系樹脂等が挙げられる。これらの樹脂は、単独で用いてもよく、2種以上を組み合わせて用いてもよい。好ましくは、ポリアミド系樹脂、ポリイミド系樹脂、ポリアミドイミド系樹脂、ポリエチレンナフタレート系樹脂、ポリカーボネート系樹脂である。耐久性および機械的強度に優れるからである。さらに好ましくは、ポリイミド系樹脂である。
A-2. Base film The base film 10 can be made of any suitable material. Specific examples of the constituent materials include polyethylene terephthalate resin, polyethylene naphthalate resin, acetate resin, polyether sulfone resin, polycarbonate resin, polyamide resin, polyimide resin, polyamideimide resin, and polyolefin resin. Examples thereof include (meth) acrylic resins, polyvinyl chloride resins, polyvinylidene chloride resins, polystyrene resins, polyvinyl alcohol resins, polyarylate resins, polyphenylene sulfide resins and the like. These resins may be used alone or in combination of two or more. Preferably, it is a polyamide-based resin, a polyimide-based resin, a polyamide-imide-based resin, a polyethylene naphthalate-based resin, or a polycarbonate-based resin. This is because it has excellent durability and mechanical strength. More preferably, it is a polyimide resin.
 基材フィルムは、上記構成材料に配合された微粒子を含んでいてもよい。より具体的には、基材フィルムは、上記構成材料のマトリックス中にナノメートルオーダーの微粒子が分散した、いわゆるナノコンポジットフィルムであってもよい。このような構成であれば、非常に優れた硬度および耐擦傷性が付与され得る。微粒子の平均粒子径は、例えば1nm~100nm程度である。微粒子は、代表的には無機酸化物で構成されている。好ましくは、微粒子は、所定の官能基で表面が修飾されている。微粒子を構成する無機酸化物としては、例えば、酸化ジルコニウム、イットリア添加酸化ジルコニウム、ジルコン酸鉛、チタン酸ストロンチウム、チタン酸スズ、酸化スズ、酸化ビスマス、酸化ニオブ、酸化タンタル、タンタル酸カリウム、酸化タングステン、酸化セリウム、酸化ランタン、酸化ガリウム等、シリカ、アルミナ、酸化チタン、酸化ジルコニウム、チタン酸バリウムが挙げられる。 The base film may contain fine particles blended in the above constituent materials. More specifically, the base film may be a so-called nanocomposite film in which nanometer-order fine particles are dispersed in the matrix of the constituent materials. With such a configuration, very good hardness and scratch resistance can be imparted. The average particle size of the fine particles is, for example, about 1 nm to 100 nm. The fine particles are typically composed of inorganic oxides. Preferably, the surface of the fine particles is modified with a predetermined functional group. Examples of the inorganic oxides constituting the fine particles include zirconium oxide, ittoria-added zirconium oxide, lead zirconate, strontium titanate, tin titanate, tin oxide, bismuth oxide, niobium oxide, tantalum oxide, potassium tantalate, and tungsten oxide. , Cerium oxide, lanthanum oxide, gallium oxide and the like, silica, alumina, titanium oxide, zirconium oxide, barium titanate and the like.
 基材フィルムの厚みは、好ましくは40μm~100μmであり、より好ましくは50μm~80μmである。このような厚みであれば、薄型化、ハンドリング性、機械的強度のバランスに優れる。 The thickness of the base film is preferably 40 μm to 100 μm, more preferably 50 μm to 80 μm. With such a thickness, the balance between thinning, handleability, and mechanical strength is excellent.
 基材フィルムの鉛筆硬度は、好ましくはB以上であり、より好ましくはF以上であり、さらに好ましくはH以上である。 The pencil hardness of the base film is preferably B or higher, more preferably F or higher, and even more preferably H or higher.
A-3.ハードコート層の形成
 ハードコート層20は、代表的には、ハードコート層形成用塗布液を塗布して塗布層を形成し、塗布層に活性エネルギー線(例えば、紫外線)を照射して硬化させることにより形成される。ハードコート層形成用塗布液は、ベース樹脂として活性エネルギー線硬化型(メタ)アクリレートを含む。活性エネルギー線硬化型(メタ)アクリレートとしては、例えば、紫外線硬化型(メタ)アクリレート、電子線硬化型(メタ)アクリレートが挙げられる。好ましくは、紫外線硬化型(メタ)アクリレートである。簡単な加工操作にて効率よくハードコート層を形成することができるからである。紫外線硬化型(メタ)アクリレートは、紫外線硬化型のモノマー、オリゴマー、ポリマー等を含む。紫外線硬化型(メタ)アクリレートは、紫外線重合官能基を好ましくは2個以上、より好ましくは3~6個有するモノマー成分およびオリゴマー成分を含む。代表的には、紫外線硬化型(メタ)アクリレートには、光重合開始剤が配合されている。硬化方式は、ラジカル重合方式であってもよく、カチオン重合方式であってもよい。1つの実施形態においては、(メタ)アクリレートにシリカ粒子やポリシルセスキオキサン化合物などを配合した有機無機ハイブリッド材料を用いてもよい。ハードコート層の構成材料および形成方法は、例えば特開2011-237789号公報に記載されている。当該公報の記載は、本明細書に参考として援用される。なお、本明細書において(メタ)アクリレートとは、アクリレートおよび/またはメタクリレートを意味する。
A-3. Formation of hard coat layer The hard coat layer 20 is typically coated with a coating liquid for forming a hard coat layer to form a coating layer, and the coating layer is irradiated with active energy rays (for example, ultraviolet rays) to be cured. Is formed by The coating liquid for forming a hard coat layer contains an active energy ray-curable (meth) acrylate as a base resin. Examples of the active energy ray-curable (meth) acrylate include an ultraviolet curable (meth) acrylate and an electron beam-curable (meth) acrylate. A UV curable (meth) acrylate is preferred. This is because the hard coat layer can be efficiently formed by a simple processing operation. The UV curable (meth) acrylate contains UV curable monomers, oligomers, polymers and the like. The UV curable (meth) acrylate contains a monomer component and an oligomer component having preferably 2 or more, more preferably 3 to 6 UV polymerization functional groups. Typically, the ultraviolet curable (meth) acrylate contains a photopolymerization initiator. The curing method may be a radical polymerization method or a cationic polymerization method. In one embodiment, an organic-inorganic hybrid material in which silica particles, a polysilsesquioxane compound, or the like is mixed with (meth) acrylate may be used. A constituent material and a method for forming the hard coat layer are described in, for example, Japanese Patent Application Laid-Open No. 2011-237789. The description of this publication is incorporated herein by reference. In addition, in this specification, (meth) acrylate means acrylate and / or methacrylate.
 紫外線硬化型(メタ)アクリレートには、スライドリング材料が配合されてもよい。スライドリング材料を配合することにより、良好な可撓性が付与され得る。スライドリング材料の代表例としてはポリロタキサンが挙げられる。ポリロタキサンは、代表的には、直鎖状のポリエチレングリコール(PEG)主鎖をシクロデキストリン(CD)環状分子がスライドする構造を有する。PEG主鎖の両末端はアダマンタンアミンで修飾され、CD環状分子の脱落が防止される。ポリロタキサンにおいては、好ましくは、CD環状分子は化学修飾されて活性エネルギー線重合性基が付与されている。スライドリング材料を用いる場合、紫外線硬化型(メタ)アクリレートとしては、ラジカル重合性基を有するラジカル重合性モノマーが好ましく用いられる。ラジカル重合性基としては、例えば、(メタ)アクリロイル基、(メタ)アクリロイルオキシ基等が挙げられる。ポリロタキサンとの相溶性に優れ、かつ、多様な材料選択が可能となるからである。ポリロタキサン(実質的には、CD環状分子の重合性基)と紫外線硬化型(メタ)アクリレートの紫外線硬化性成分とが反応して硬化すると、硬化後においても架橋点が可動であるハードコート層が得られる。その結果、折り曲げ時の応力を緩和することができ、折り曲げ耐久性が向上する。ポリロタキサンおよび硬化メカニズムは、例えば特開2015-155530号公報に記載されている。当該公報の記載は、本明細書に参考として援用される。 A slide ring material may be blended with the ultraviolet curable (meth) acrylate. Good flexibility can be imparted by blending the slide ring material. Polyrotaxane is a typical example of the slide ring material. Polyrotaxane typically has a structure in which a cyclodextrin (CD) cyclic molecule slides on a linear polyethylene glycol (PEG) main chain. Both ends of the PEG backbone are modified with adamantaneamine to prevent shedding of the CD cyclic molecule. In polyrotaxane, preferably, the CD cyclic molecule is chemically modified to impart an active energy ray-polymerizable group. When a slide ring material is used, a radically polymerizable monomer having a radically polymerizable group is preferably used as the ultraviolet curable (meth) acrylate. Examples of the radically polymerizable group include a (meth) acryloyl group and a (meth) acryloyloxy group. This is because it has excellent compatibility with polyrotaxane and various material selections are possible. When polyrotaxane (substantially a polymerizable group of a CD cyclic molecule) reacts with an ultraviolet curable component of an ultraviolet curable (meth) acrylate and is cured, a hard coat layer in which the cross-linking point is movable even after curing is formed. can get. As a result, the stress at the time of bending can be relaxed, and the bending durability is improved. Polyrotaxane and the curing mechanism are described in, for example, Japanese Patent Application Laid-Open No. 2015-155530. The description of this publication is incorporated herein by reference.
 紫外線硬化型(メタ)アクリレートには、ナノファイバーおよび/またはナノクリスタルが配合されてもよい。ナノファイバーの代表例としては、セルロースナノファイバー、キチンナノファイバー、キトサンナノファイバーが挙げられる。これらを配合することにより、優れた透明性を維持しつつ、可撓性、鉛筆硬度、耐擦傷性、耐摩耗性に優れたハードコート層が得られ得る。ナノファイバーおよび/またはナノクリスタル(組み合わせて用いる場合にはその合計)は、ハードコート層全体に対して好ましくは0.1重量%~40重量%の割合で配合され得る。ナノファイバーは、平均繊維径が例えば1nm~100nmであり、平均繊維長が例えば10nm~1000nmである。ナノファイバーを含むハードコート層は、例えば特開2012-131201号公報、特開2012-171171号公報に記載されている。当該公報の記載は、本明細書に参考として援用される。 The ultraviolet curable (meth) acrylate may contain nanofibers and / or nanocrystals. Typical examples of nanofibers include cellulose nanofibers, chitin nanofibers, and chitosan nanofibers. By blending these, a hard coat layer having excellent flexibility, pencil hardness, scratch resistance, and abrasion resistance can be obtained while maintaining excellent transparency. The nanofibers and / or nanocrystals (the total when used in combination) can be blended in a proportion of 0.1% to 40% by weight, preferably 0.1% by weight, based on the entire hard coat layer. Nanofibers have an average fiber diameter of, for example, 1 nm to 100 nm, and an average fiber length of, for example, 10 nm to 1000 nm. The hard coat layer containing nanofibers is described in, for example, Japanese Patent Application Laid-Open No. 2012-131201 and Japanese Patent Application Laid-Open No. 2012-171171. The description of this publication is incorporated herein by reference.
 塗布液は、目的に応じて任意の適切な添加剤をさらに含んでいてもよい。添加剤としては、例えば、光重合開始剤、レベリング剤、ブロッキング防止剤、分散安定剤、揺変剤、酸化防止剤、紫外線吸収剤、消泡剤、増粘剤、分散剤、界面活性剤、触媒、フィラー、滑剤、帯電防止剤等が挙げられる。含有される添加剤の種類、組み合わせ、含有量等は、目的や所望の特性に応じて適切に設定され得る。 The coating liquid may further contain any suitable additive depending on the purpose. Additives include, for example, photopolymerization initiators, leveling agents, blocking inhibitors, dispersion stabilizers, rockers, antioxidants, UV absorbers, defoamers, thickeners, dispersants, surfactants, etc. Examples thereof include catalysts, fillers, lubricants, and antistatic agents. The type, combination, content, etc. of the additives contained can be appropriately set according to the purpose and desired characteristics.
 活性エネルギー線(例えば、紫外線)の照射量(積算光量)は、例えば150mJ/cm~400mJ/cmである。必要に応じて、活性エネルギー線照射前に塗布層を加熱してもよい。加熱温度は、例えば70℃~100℃である。加熱時間は、例えば1分~4分である。 Active energy ray (e.g., ultraviolet) irradiation amount (integrated light quantity) is, for example, 150mJ / cm 2 ~ 400mJ / cm 2. If necessary, the coating layer may be heated before irradiation with active energy rays. The heating temperature is, for example, 70 ° C to 100 ° C. The heating time is, for example, 1 minute to 4 minutes.
 形成されるハードコート層の厚みは、好ましくは3μm~20μmであり、より好ましくは3μm~15μmである。厚みがこのような範囲であれば、カールを良好に抑制するとともに、優れた表面硬度と屈曲性および/または折りたたみ性とを両立することができる。 The thickness of the formed hard coat layer is preferably 3 μm to 20 μm, and more preferably 3 μm to 15 μm. When the thickness is in such a range, curling can be satisfactorily suppressed, and both excellent surface hardness and flexibility and / or foldability can be achieved at the same time.
A-4.保護フィルムの積層
 保護フィルム40は、代表的には、基材フィルム/ハードコート層の積層体のハードコート層の表面にロールトゥロールにより積層され得る。保護フィルムの第1の方向の熱収縮率および第1の方向に直交する第2の方向の熱収縮率のうち大きいほうの熱収縮率は0.1%以下であり、好ましくは0.08%以下であり、より好ましくは0.06%以下であり、さらに好ましくは0.05%以下である。当該熱収縮率は小さいほど好ましい。当該熱収縮率の下限は、例えば0.01%であり得る。当該熱収縮率がこのような範囲であれば、印刷層付フィルム積層体のカール(特に、印刷層形成時の加熱によるカール)が顕著に抑制され得る。第1の方向は、代表的には、保護フィルムの搬送方向である。
A-4. Lamination of Protective Film The protective film 40 can be typically laminated by roll-to-roll on the surface of the hard coat layer of the laminate of the base film / hard coat layer. The larger of the heat shrinkage rate in the first direction and the heat shrinkage rate in the second direction orthogonal to the first direction of the protective film is 0.1% or less, preferably 0.08%. It is less than or equal to, more preferably 0.06% or less, still more preferably 0.05% or less. The smaller the heat shrinkage, the more preferable. The lower limit of the heat shrinkage rate can be, for example, 0.01%. When the heat shrinkage rate is within such a range, curl of the film laminate with a print layer (particularly, curl due to heating at the time of forming the print layer) can be remarkably suppressed. The first direction is typically the transport direction of the protective film.
 保護フィルムの熱収縮率については、代表的には、搬送方向の熱収縮率が搬送方向に直交する方向(幅方向)の熱収縮率より大きい。保護フィルムにおけるこのような熱収縮率に関する特性は、ガラス転移温度を低くすること、または、線膨張係数を高くすることにより実現され得る。 Regarding the heat shrinkage rate of the protective film, typically, the heat shrinkage rate in the transport direction is larger than the heat shrinkage rate in the direction orthogonal to the transport direction (width direction). Such properties regarding the coefficient of thermal shrinkage in the protective film can be realized by lowering the glass transition temperature or increasing the coefficient of linear expansion.
 保護フィルムは、上記のような熱収縮率を実現し得る任意の適切な材料で構成され得る。構成材料の具体例としては、ポリエチレンテレフタレート等のポリエステル系樹脂、ノルボルネン系樹脂等のシクロオレフィン系樹脂、ポリアミド系樹脂、ポリカーボネート系樹脂、これらの共重体樹脂等が挙げられる。好ましくはポリエステル系樹脂であり、より好ましくはポリエチレンテレフタレートである。 The protective film can be made of any suitable material that can achieve the heat shrinkage as described above. Specific examples of the constituent materials include polyester resins such as polyethylene terephthalate, cycloolefin resins such as norbornene resins, polyamide resins, polycarbonate resins, and copolymer resins thereof. A polyester resin is preferable, and polyethylene terephthalate is more preferable.
 保護フィルムの厚みは、好ましくは30μm~140μmであり、好ましくは35μm~135μmである。このような厚みであれば、上記熱収縮率に関する特性との相乗的な効果により、印刷層付フィルム積層体のカールを顕著に抑制することができる。なお、保護フィルムは上記のとおりベースフィルム(樹脂フィルム)と粘着剤層とを含み、保護フィルムの厚みはベースフィルムと粘着剤層の合計厚みである。 The thickness of the protective film is preferably 30 μm to 140 μm, preferably 35 μm to 135 μm. With such a thickness, curling of the film laminate with a print layer can be remarkably suppressed due to a synergistic effect with the above-mentioned characteristics related to the heat shrinkage rate. As described above, the protective film includes the base film (resin film) and the pressure-sensitive adhesive layer, and the thickness of the protective film is the total thickness of the base film and the pressure-sensitive adhesive layer.
 保護フィルムの弾性率は、好ましくは2.2kN/mm~4.8kN/mmである。保護フィルムの弾性率がこのような範囲であれば、印刷層付フィルム積層体のカール抑制に貢献することができる。なお、弾性率は、JIS K 6781に準拠して測定される。 The elastic modulus of the protective film is preferably 2.2 kN / mm 2 to 4.8 kN / mm 2 . When the elastic modulus of the protective film is within such a range, it can contribute to curl suppression of the film laminate with the print layer. The elastic modulus is measured according to JIS K 6781.
 保護フィルムの引張伸度は、好ましくは90%~170%である。保護フィルムの引張伸度がこのような範囲であれば、搬送中に破断しにくいという利点を有する。なお、引張伸度は、JIS K 6781に準拠して測定される。 The tensile elongation of the protective film is preferably 90% to 170%. When the tensile elongation of the protective film is within such a range, it has an advantage that it is unlikely to break during transportation. The tensile elongation is measured in accordance with JIS K6781.
A-5.印刷層の形成
 印刷層30は、代表的には、保護フィルム積層後に形成され得る。より詳細には、印刷層は、基材フィルム/ハードコート層/保護フィルムの積層体を所定サイズおよび所定形状に裁断した後に形成され得る。裁断に関して、例えば、当該積層体を矩形に裁断する場合、当該積層体の長尺方向(搬送方向)が長辺方向となるように矩形に裁断してもよく、短辺方向となるように矩形に裁断してもよい。
A-5. Formation of Print Layer The print layer 30 can typically be formed after laminating the protective film. More specifically, the print layer may be formed after the laminate of the base film / hard coat layer / protective film is cut into a predetermined size and shape. Regarding cutting, for example, when the laminated body is cut into a rectangular shape, the laminated body may be cut into a rectangular shape so that the long side direction (transportation direction) of the laminated body is the long side direction, or the rectangular body is cut into a rectangular shape so as to be the short side direction. You may cut it into.
 印刷層は、任意の適切なインキまたは塗料を用いた任意の適切な印刷法により形成することができる。印刷法の具体例としては、グラビア印刷、オフセット印刷、シルクスクリーン印刷、転写シートからの転写印刷が挙げられる。 The print layer can be formed by any suitable printing method using any suitable ink or paint. Specific examples of the printing method include gravure printing, offset printing, silk screen printing, and transfer printing from a transfer sheet.
 使用されるインキまたは塗料は、代表的には、バインダーと着色剤と溶媒と必要に応じて用いられ得る任意の適切な添加剤とを含む。バインダーとしては、塩素化ポリオレフィン(例えば、塩素化ポリエチレン、塩素化ポリプロピレン)、ポリエステル系樹脂、ウレタン系樹脂、アクリル系樹脂、酢酸ビニル樹脂、塩化ビニル-酢酸ビニル共重合体、セルロース系樹脂が挙げられる。バインダー樹脂は、単独で用いてもよく2種以上を併用してもよい。1つの実施形態においては、バインダー樹脂は熱重合性樹脂である。熱重合性樹脂は、光重合性樹脂に比べて使用量が少なくてすむので、着色剤の使用量(着色層における着色剤含有量)を増大させることができる。その結果、特に黒色の着色層を形成する場合に、全光線透過率が非常に小さく、優れた隠蔽性を有する着色層を形成することができる。1つの実施形態においては、バインダー樹脂は(メタ)アクリル系樹脂であり、好ましくは多官能モノマー(例えば、ペンタエリスリトールトリ(メタ)アクリレート)を共重合成分として含む(メタ)アクリル系樹脂である。多官能モノマーを共重合成分として含む(メタ)アクリル系樹脂を用いることにより、適切な弾性率を有する印刷層が形成され得る。加えて、印刷層の厚みによる段差も形成され、当該段差がブロッキング防止に効果的に機能し得る。 The ink or paint used typically includes a binder, a colorant, a solvent and any suitable additive that may be used as needed. Examples of the binder include chlorinated polyolefins (for example, chlorinated polyethylene and chlorinated polypropylene), polyester resins, urethane resins, acrylic resins, vinyl acetate resins, vinyl chloride-vinyl acetate copolymers, and cellulose resins. .. The binder resin may be used alone or in combination of two or more. In one embodiment, the binder resin is a thermosetting resin. Since the thermosetting resin can be used in a smaller amount than the photopolymerizable resin, the amount of the colorant used (colorant content in the colored layer) can be increased. As a result, especially when forming a black colored layer, it is possible to form a colored layer having a very small total light transmittance and excellent hiding power. In one embodiment, the binder resin is a (meth) acrylic resin, preferably a (meth) acrylic resin containing a polyfunctional monomer (eg, pentaerythritol tri (meth) acrylate) as a copolymerization component. By using a (meth) acrylic resin containing a polyfunctional monomer as a copolymerization component, a printed layer having an appropriate elastic modulus can be formed. In addition, a step is also formed due to the thickness of the print layer, and the step can effectively function to prevent blocking.
 着色剤としては、目的および所望の色に応じて任意の適切な着色剤が用いられ得る。着色剤の具体例としては、チタン白、亜鉛華、カーボンブラック、鉄黒、弁柄、クロムバーミリオン、群青、コバルトブルー、黄鉛、チタンイエロー等の無機顔料;フタロシアニンブルー、インダスレンブルー、イソインドリノンイエロー、ベンジジンイエロー、キナクリドンレッド、ポリアゾレッド、ペリレンレッド、アニリンブラック等の有機顔料または染料;アルミニウム、真鍮等の鱗片状箔片からなる金属顔料;二酸化チタン被覆雲母、塩基性炭酸鉛等の鱗片状箔片からなる真珠光沢顔料(パール顔料)が挙げられる。黒色の着色層を形成する場合には、カーボンブラック、鉄黒、アニリンブラックが好適に用いられる。この場合、着色剤は併用することが好ましい。可視光を広範囲かつ均等に吸収し、色付きのない(すなわち、真っ黒な)着色層を形成し得るからである。例えば、上記の着色剤に加えて、アゾ化合物および/またはキノン化合物が用いられ得る。1つの実施形態においては、着色剤は、主成分としてのカーボンブラックとその他の着色剤(例えば、アゾ化合物および/またはキノン化合物)とを含む。このような構成によれば、色つきがなく、かつ、経時安定性に優れた着色層を形成し得る。黒色の着色層を形成する場合には、着色剤は、バインダー樹脂100重量部に対して、好ましくは50重量部~200重量部の割合で用いられ得る。この場合、着色剤中のカーボンブラックの含有割合は、好ましくは80%~100%である。このような割合で着色剤(特にカーボンブラック)を用いることにより、全光線透過率が非常に小さく、かつ、経時安定性に優れた着色層を形成することができる。 As the colorant, any suitable colorant can be used depending on the purpose and the desired color. Specific examples of colorants include inorganic pigments such as titanium white, zinc flower, carbon black, iron black, valve handle, chrome vermilion, ultramarine blue, cobalt blue, yellow lead, and titanium yellow; phthalocyanine blue, induslen blue, and iso. Organic pigments or dyes such as indolinone yellow, benzidine yellow, quinacridone red, polyazo red, perylene red, aniline black; metal pigments composed of scaly foil pieces such as aluminum and brass; scales such as titanium dioxide coated mica and basic lead carbonate. Examples thereof include pearl luster pigments (pearl pigments) composed of shaped foil pieces. When forming a black colored layer, carbon black, iron black, and aniline black are preferably used. In this case, it is preferable to use a colorant in combination. This is because it can absorb visible light over a wide range and evenly to form a non-colored (ie, black) colored layer. For example, in addition to the colorants described above, azo compounds and / or quinone compounds can be used. In one embodiment, the colorant comprises carbon black as a main component and other colorants (eg, azo compounds and / or quinone compounds). According to such a configuration, it is possible to form a colored layer that is not colored and has excellent stability over time. When forming a black colored layer, the colorant can be used in a ratio of preferably 50 parts by weight to 200 parts by weight with respect to 100 parts by weight of the binder resin. In this case, the content ratio of carbon black in the colorant is preferably 80% to 100%. By using a colorant (particularly carbon black) at such a ratio, it is possible to form a colored layer having a very small total light transmittance and excellent stability over time.
 形成される印刷層は、用途および所望のデザインに応じて印刷により着色されている着色層である。印刷層の色としては、例えば、黒色、褐色、白色、紺色、赤色、金色、銀色が挙げられる。印刷層は、所定のデザインが施された意匠層であってもよく、ベタの着色層であってもよい。印刷層は、好ましくはベタの着色層であり、より好ましくは黒色の着色層である。印刷層を黒色の着色層とすることにより、非表示領域において配線、端子、バックライト、その他の部品を隠蔽することができる。すなわち、印刷層は隠蔽層として機能し得る。印刷層は、目的に応じた任意の適切なパターンで形成され得る。1つの実施形態においては、印刷層は、ベゼルに対応する位置に形成され得る。このような構成であれば、ベゼルを用いずに非表示領域を隠蔽することができるので、ベゼルを用いない画像表示装置を実現することができる。その結果、最表面に段差のない、きわめて優れた外観を有する画像表示装置を提供することができる。 The printed layer formed is a colored layer that is colored by printing according to the application and the desired design. Examples of the color of the print layer include black, brown, white, dark blue, red, gold, and silver. The printing layer may be a design layer having a predetermined design, or may be a solid colored layer. The printing layer is preferably a solid colored layer, and more preferably a black colored layer. By using a black colored layer as the print layer, wiring, terminals, a backlight, and other parts can be concealed in a non-display area. That is, the print layer can function as a concealment layer. The print layer can be formed in any suitable pattern depending on the purpose. In one embodiment, the print layer may be formed in a position corresponding to the bezel. With such a configuration, the non-display area can be concealed without using a bezel, so that an image display device that does not use a bezel can be realized. As a result, it is possible to provide an image display device having an extremely excellent appearance with no step on the outermost surface.
 形成される印刷層の厚みは、好ましくは3μm~15μmである。さらに、印刷層は、厚み3μm~15μmにおける全光線透過率が好ましくは0.01%以下であり、より好ましくは0.008%以下である。全光線透過率がこのような範囲であれば、ベゼルを用いることなく画像表示装置の非表示領域を良好に隠蔽することができる。 The thickness of the printed layer formed is preferably 3 μm to 15 μm. Further, the printed layer has a total light transmittance of preferably 0.01% or less, more preferably 0.008% or less at a thickness of 3 μm to 15 μm. When the total light transmittance is in such a range, the non-display area of the image display device can be well concealed without using the bezel.
 以上のようにして、印刷層付フィルム積層体が作製される。 As described above, a film laminate with a print layer is produced.
A-6.印刷層の加熱乾燥
 次いで、印刷層付フィルム積層体の印刷層を加熱乾燥することにより、最終的な印刷層付フィルム積層体が得られ得る。すなわち、印刷層の加熱乾燥は、保護フィルムを積層した状態で行われる。保護フィルムを積層した状態で印刷層を加熱乾燥することにより、カールを顕著に抑制することができる。加熱乾燥は、代表的には、40℃以上で20分以上行われる。加熱温度は、好ましくは50℃以上であり、より好ましくは60℃以上であり、さらに好ましくは70℃以上である。加熱温度の上限は、例えば95℃であり得る。加熱時間は、好ましくは30分以上であり、より好ましくは40分以上であり、さらに好ましくは50分以上であり、特に好ましくは60分以上である。加熱時間の上限は、例えば90分であり得る。加熱温度が高すぎるおよび/または加熱時間が長すぎると、印刷層付フィルム積層体のカールが大きくなる、および/または、印刷層付フィルム積層体が熱で軟化または溶融して破断してしまう場合がある。加熱温度が低すぎるおよび/または加熱時間が短すぎると、印刷層が十分に形成されない場合がある。
A-6. Heat-drying of the print layer Next, by heat-drying the print layer of the film laminate with the print layer, the final film laminate with the print layer can be obtained. That is, the heat-drying of the print layer is performed in a state where the protective films are laminated. Curling can be remarkably suppressed by heating and drying the print layer in a state where the protective films are laminated. Heat drying is typically performed at 40 ° C. or higher for 20 minutes or longer. The heating temperature is preferably 50 ° C. or higher, more preferably 60 ° C. or higher, and even more preferably 70 ° C. or higher. The upper limit of the heating temperature can be, for example, 95 ° C. The heating time is preferably 30 minutes or more, more preferably 40 minutes or more, still more preferably 50 minutes or more, and particularly preferably 60 minutes or more. The upper limit of the heating time can be, for example, 90 minutes. If the heating temperature is too high and / or the heating time is too long, the curl of the film laminate with the print layer becomes large, and / or the film laminate with the print layer softens or melts due to heat and breaks. There is. If the heating temperature is too low and / or the heating time is too short, the print layer may not be sufficiently formed.
A-7.その他
 実用的には、得られた印刷層付フィルム積層体の印刷層および基材フィルム表面には、工程保護フィルムが剥離可能に仮着される。工程保護フィルムが仮着された印刷層付フィルム積層体は、アラインメントカット、出荷前検査等に供される。印刷層付フィルム積層体の実用時には、保護フィルムおよび工程保護フィルムは剥離除去される。代表的には、保護フィルムが工程保護フィルムよりも後に(実質的には、最後に)剥離除去される。
A-7. Others Practically, a process protection film is temporarily attached to the print layer and the surface of the base film of the obtained film laminate with a print layer so as to be peelable. The film laminate with a print layer to which the process protection film is temporarily attached is used for alignment cutting, pre-shipment inspection, and the like. In practical use, the protective film and the process protective film are peeled off and removed. Typically, the protective film is stripped off (substantially at the end) after the process protective film.
A-8.得られる印刷層付フィルム積層体の特性
 印刷層付フィルム積層体は、70℃の環境下に60分置いた後の反り量が19mm以下であり、好ましくは15mm以下であり、より好ましくは10mm以下であり、さらに好ましくは7mm以下である。反り量は小さいほど好ましい。反り量の下限は、例えば2mmであり得る。本発明の実施形態によれば、印刷層付フィルム積層体において、反り量(カール)をこのように非常に小さくすることができる。その結果、印刷層付フィルム積層体は、確実かつ良好に光学フィルムまたは画像表示セルに積層することができる。
A-8. Characteristics of the obtained film laminate with print layer The film laminate with print layer has a warp amount of 19 mm or less, preferably 15 mm or less, more preferably 10 mm or less after being placed in an environment of 70 ° C. for 60 minutes. It is more preferably 7 mm or less. The smaller the amount of warpage, the more preferable. The lower limit of the amount of warpage can be, for example, 2 mm. According to the embodiment of the present invention, the amount of warpage (curl) can be made very small in the film laminate with a print layer. As a result, the film laminate with the print layer can be reliably and satisfactorily laminated on the optical film or the image display cell.
 印刷層付フィルム積層体の視認側表面(実質的には、ハードコート層表面)は、好ましくは2H以上、より好ましくは3H以上、さらに好ましくは4H以上の鉛筆硬度を有する。鉛筆硬度がこのような範囲であれば、印刷層付フィルム積層体がウィンドウフィルムとして良好に機能し得る。鉛筆硬度は、JIS K 5400-5-4に準じて測定され得る。さらに、当該視認側表面は、1000g荷重で好ましくは300回、より好ましくは500回、さらに好ましくは1000回往復摩擦しても傷を生じない耐擦傷性を有する。なお、耐擦傷性は、スチールウール#0000を用いて所定荷重(例えば、500g/cm、1000g/cm)で表面を所定の回数往復した際の傷の状態にて評価され得る。 The visible side surface (substantially the surface of the hard coat layer) of the film laminate with the printing layer has a pencil hardness of preferably 2H or more, more preferably 3H or more, still more preferably 4H or more. When the pencil hardness is in such a range, the film laminate with a print layer can function well as a window film. Pencil hardness can be measured according to JIS K 5400-5-4. Further, the visible surface has scratch resistance that does not cause scratches even if it is rubbed back and forth preferably 300 times, more preferably 500 times, and even more preferably 1000 times under a load of 1000 g. The scratch resistance can be evaluated in the state of scratches when steel wool # 0000 is used and the surface is reciprocated a predetermined number of times under a predetermined load (for example, 500 g / cm 2 , 1000 g / cm 2).
 印刷層付フィルム積層体は、曲率半径3mm以下(例えば、3mm、2mm、1mm)で好ましくは5万回、より好ましくは10万回、さらに好ましくは20万回折り曲げ可能な屈曲性を有する。印刷層付フィルム積層体がこのような屈曲性を有することにより、印刷層付フィルム積層体を画像表示装置に適用した場合に屈曲可能または折り畳み可能な画像表示装置を実現することができる。屈曲性の試験は、ハードコート層を内側にして折り曲げて行われる。具体的には、屈曲性試験は、印刷層付フィルム積層体を100mm×20mmの短冊状に切り出して測定サンプルとし、試験機(ユアサシステム機器(株)製「CL09-typeD01-FMC90」)に、ハードコート層側を屈曲の内側となるように測定サンプルセットし、下記の条件で行う。屈曲性の評価は、試験後のサンプルの屈曲部分における剥離の状態を目視で観察することで判断し得る。
 環境条件:25℃、55%RH
 試験速度:60rpm
The film laminate with a printing layer has a radius of curvature of 3 mm or less (for example, 3 mm, 2 mm, 1 mm) and has flexibility that allows it to bend preferably 50,000 times, more preferably 100,000 times, and even more preferably 200,000 times. Since the film laminate with a print layer has such flexibility, it is possible to realize an image display device that is bendable or foldable when the film laminate with a print layer is applied to an image display device. The flexibility test is performed by bending with the hard coat layer inside. Specifically, in the flexibility test, a film laminate with a print layer is cut out into a strip of 100 mm × 20 mm and used as a measurement sample, and the test machine (“CL09-typeD01-FMC90” manufactured by Yuasa System Co., Ltd.) is used. Set the measurement sample so that the hard coat layer side is inside the bend, and perform under the following conditions. The evaluation of the flexibility can be judged by visually observing the state of peeling at the bent portion of the sample after the test.
Environmental conditions: 25 ° C, 55% RH
Test speed: 60 rpm
 印刷層付フィルム積層体(印刷層を除く)の光線透過率は、好ましくは85%以上であり、より好ましくは87%以上であり、さらに好ましくは90%以上である。印刷層付フィルム積層体(印刷層を除く)のヘイズは、好ましくは1.5%以下であり、より好ましくは1.2%以下であり、さらに好ましくは1.0%以下である。光線透過率および/またはヘイズがこのような範囲であれば、印刷層付フィルム積層体が画像表示装置に適用された場合に良好な視認性を実現することができる。 The light transmittance of the film laminate with a print layer (excluding the print layer) is preferably 85% or more, more preferably 87% or more, and further preferably 90% or more. The haze of the film laminate with a print layer (excluding the print layer) is preferably 1.5% or less, more preferably 1.2% or less, and further preferably 1.0% or less. When the light transmittance and / or haze is in such a range, good visibility can be realized when the film laminate with a print layer is applied to an image display device.
 印刷層付フィルム積層体は、例えば、画像表示装置のウィンドウフィルム、カーナビゲーションシステムの前面板、ヘッドアップディスプレイシステムのダストカバーとして好適に用いられ得る。 The film laminate with a print layer can be suitably used as, for example, a window film of an image display device, a front plate of a car navigation system, and a dust cover of a head-up display system.
B.光学積層体
 印刷層付フィルム積層体は、光学フィルムが積層されて光学積層体を構成し得る。図2は、図1の印刷層付フィルム積層体を含む光学積層体の概略断面図である。図示例の光学積層体200は、印刷層付フィルム積層体100と光学フィルム120とを有する。光学フィルム120は、印刷層付フィルム積層体100における基材フィルム10のハードコート層20と反対側に配置されている。光学フィルム120は、代表的には、接着層140を介して印刷層付フィルム積層体100に積層されている。接着層は、目的に応じた任意の適切な粘着剤または接着剤で構成されている。
B. Optical Laminated A film laminate with a print layer may be formed by laminating optical films to form an optical laminate. FIG. 2 is a schematic cross-sectional view of an optical laminate including the film laminate with a print layer of FIG. The optical laminate 200 of the illustrated example has a film laminate 100 with a print layer and an optical film 120. The optical film 120 is arranged on the side opposite to the hard coat layer 20 of the base film 10 in the film laminate 100 with a print layer. The optical film 120 is typically laminated on the film laminate 100 with a print layer via an adhesive layer 140. The adhesive layer is composed of any suitable adhesive or adhesive depending on the purpose.
 印刷層付フィルム積層体100は、上記A項に記載のとおりである。 The film laminate 100 with a print layer is as described in item A above.
 光学フィルム120としては、任意の適切な光学フィルムが挙げられる。光学フィルムは、単一層で構成されるフィルムであってもよく、積層体であってもよい。単一層で構成される光学フィルムの具体例としては、偏光子、位相差フィルムが挙げられる。積層体として構成される光学フィルムの具体例としては、偏光板(代表的には、偏光子と保護フィルムとの積層体)、タッチパネル用導電性フィルム、表面処理フィルム、ならびに、これらの単一層で構成される光学フィルムおよび/または積層体として構成される光学フィルムを目的に応じて適切に積層した積層体(例えば、反射防止用円偏光板、タッチパネル用導電層付偏光板)が挙げられる。 Examples of the optical film 120 include any suitable optical film. The optical film may be a film composed of a single layer or a laminated body. Specific examples of the optical film composed of a single layer include a polarizer and a retardation film. Specific examples of the optical film configured as a laminate include a polarizing plate (typically, a laminate of a polarizing element and a protective film), a conductive film for a touch panel, a surface treatment film, and a single layer thereof. Examples thereof include a laminated body (for example, a circular polarizing plate for antireflection, a polarizing plate with a conductive layer for a touch panel) in which an optical film formed as an optical film and / or an optical film formed as a laminated body is appropriately laminated according to a purpose.
 光学積層体200は、印刷層付フィルム積層体100における基材フィルム10のハードコート層20と反対側に光学フィルム120を積層することにより作製され得る。光学フィルム120を積層した後、保護フィルム40は剥離される。 The optical laminate 200 can be produced by laminating the optical film 120 on the side opposite to the hard coat layer 20 of the base film 10 in the film laminate 100 with a print layer. After laminating the optical film 120, the protective film 40 is peeled off.
C.画像表示装置
 上記A項に記載の印刷層付フィルム積層体および上記B項に記載の光学積層体は、画像表示装置に適用され得る。画像表示装置の代表例としては、液晶表示装置、エレクトロルミネセンス(EL)表示装置(例えば、有機EL表示装置、無機EL表示装置)が挙げられる。画像表示装置は、代表的には、画像表示セルの視認側に印刷層付フィルム積層体または光学積層体を備える。画像表示装置は、好ましくは有機EL表示装置である。1つの実施形態においては、画像表示装置は、湾曲した形状(実質的には、湾曲した表示画面)を有し、および/または、屈曲もしくは折り曲げ可能である。より好ましくは、画像表示装置は折り畳み可能である。
C. Image Display Device The film laminate with a print layer according to item A and the optical laminate according to item B can be applied to an image display device. Typical examples of the image display device include a liquid crystal display device and an electroluminescence (EL) display device (for example, an organic EL display device and an inorganic EL display device). The image display device typically includes a film laminate with a print layer or an optical laminate on the visual side of the image display cell. The image display device is preferably an organic EL display device. In one embodiment, the image display device has a curved shape (substantially a curved display screen) and / or is bendable or bendable. More preferably, the image display device is foldable.
 画像表示装置は、画像表示セル(図示せず)の視認側に光学フィルム120および印刷層付フィルム積層体100を積層することにより作製され得る。光学フィルム120および印刷層付フィルム積層体100を積層した後、保護フィルム40は剥離される。あるいは、画像表示装置は、画像表示セル(図示せず)の視認側に光学積層体200を積層することにより作製され得る。光学積層体200を積層した後、保護フィルム40は剥離される。 The image display device can be manufactured by laminating the optical film 120 and the film laminate 100 with a print layer on the visual side of the image display cell (not shown). After laminating the optical film 120 and the film laminate 100 with a print layer, the protective film 40 is peeled off. Alternatively, the image display device can be manufactured by laminating the optical laminate 200 on the visual side of the image display cell (not shown). After laminating the optical laminate 200, the protective film 40 is peeled off.
 以下、実施例によって本発明を具体的に説明するが、本発明はこれら実施例によって限定されるものではない。各特性の測定方法は以下の通りである。
(1)厚み
 ミツトヨ製マイクロゲージ式厚み計にて測定した。基材フィルム/ハードコート層の積層体の厚みを測定し、基材フィルムの厚みを差し引くことでハードコート層の厚みを算出した。
(2)保護フィルムの熱収縮率
 実施例および比較例で用いた保護フィルムを長尺方向100mmおよび幅方向100mmのサイズに切り出して試験サンプルとした。この試験サンプルの初期の寸法を、ミツトヨ社製画像測定機「QVA606-PRO_AE10」を用いて測定した。次いで、試験サンプルを70℃で60分間加熱した後、再度寸法を測定した。以下の式から熱収縮率を算出した。なお、寸法測定は、長尺方向に対応する方向の寸法について行った。
   熱収縮率(%)={(初期寸法-加熱後寸法)/(初期寸法)}×100
(3)反り量
 実施例および比較例で得られた最終的な(乾燥後の)印刷層付フィルム積層体を平面上に静置し、4つの隅部の平面からの高さを測定し、高さが一番大きい隅部の高さを反り量とした。
(4)鉛筆硬度
 実施例および比較例において形成されたハードコート層表面について、JIS K 5600-5-4の鉛筆硬度試験に準じて(但し、荷重750g)、鉛筆硬度を測定した。
Hereinafter, the present invention will be specifically described with reference to Examples, but the present invention is not limited to these Examples. The measurement method of each characteristic is as follows.
(1) Thickness Measured with a micro gauge type thickness gauge manufactured by Mitutoyo. The thickness of the base film / hard coat layer laminate was measured, and the thickness of the hard coat layer was calculated by subtracting the thickness of the base film.
(2) Heat Shrinkage Rate of Protective Film The protective film used in Examples and Comparative Examples was cut into sizes of 100 mm in the long direction and 100 mm in the width direction to prepare test samples. The initial dimensions of this test sample were measured using an image measuring machine "QVA606-PRO_AE10" manufactured by Mitutoyo. The test sample was then heated at 70 ° C. for 60 minutes and then sized again. The heat shrinkage was calculated from the following formula. The dimensional measurement was performed for the dimensions in the direction corresponding to the long direction.
Heat shrinkage rate (%) = {(Initial dimension-Dimension after heating) / (Initial dimension)} x 100
(3) Warpage amount The final (after drying) film laminate with a print layer obtained in Examples and Comparative Examples was allowed to stand on a flat surface, and the heights of the four corners from the flat surface were measured. The height of the corner with the highest height was taken as the amount of warpage.
(4) Pencil hardness With respect to the surface of the hard coat layer formed in Examples and Comparative Examples, the pencil hardness was measured according to the pencil hardness test of JIS K 5600-5-4 (however, the load was 750 g).
<実施例1>
1.ハードコート層形成用塗布液の調製
 ベース樹脂としての紫外線硬化型多官能アクリレート(アイカ工業社製、製品名「Z-850-16」)100質量部、レベリング剤(DIC社製、商品名:GRANDIC PC-4100)5質量部、および光重合開始剤(チバ・ジャパン社製、商品名:イルガキュア907)3質量部を混合し、固形分濃度が50質量%となるようにメチルイソブチルケトンで希釈して、ハードコート層形成用塗布液を調製した。
<Example 1>
1. 1. Preparation of coating liquid for forming hard coat layer 100 parts by mass of ultraviolet curable polyfunctional acrylate (manufactured by Aika Kogyo Co., Ltd., product name "Z-850-16") as base resin, leveling agent (manufactured by DIC Co., Ltd., product name: GRANDIC) PC-4100) 5 parts by mass and 3 parts by mass of a photopolymerization initiator (manufactured by Ciba Japan, trade name: Irgacure 907) are mixed and diluted with methylisobutylketone so that the solid content concentration becomes 50% by mass. To prepare a coating liquid for forming a hard coat layer.
2.保護フィルムの作製
 攪拌羽根、温度計、窒素ガス導入管、冷却器を備えた四つ口フラスコに、ブチルアクリレート(BA)90重量部、アクリル酸(AA)10重量部、重合開始剤として2,2’-アゾビスイソブチロニトリル0.2重量部、酢酸エチル234重量部を仕込み、緩やかに攪拌しながら窒素ガスを導入し、フラスコ内の液温を63℃付近に保って約7時間重合反応を行い、アクリル系ポリマー(A)溶液(30重量%)を調製した。アクリル系ポリマー(A)の重量平均分子量は60万であり、Tgは-50℃であった。アクリル系ポリマー(A)溶液(30重量%)を酢酸エチルで20重量%に希釈し、この溶液のアクリル系ポリマー100重量部(固形分)に対して、架橋剤としてエポキシ系架橋剤(三菱ガス化学(株)製、TETRAD-C)11重量部を加えて、25℃付近に保って約1分間混合撹拌を行い、アクリル系粘着剤組成物を調製した。
 上記アクリル系粘着剤組成物を、ポリエチレンテレフタレート(PET)基材(厚み110μm)の片面に塗布し、140℃で60秒間加熱して、厚さ20μmの粘着剤層を形成することで保護フィルム(厚み130μm)を作製した。得られた保護フィルムの熱収縮率は0.04%であった。
2. Preparation of protective film In a four-necked flask equipped with a stirring blade, a thermometer, a nitrogen gas introduction tube, and a cooler, 90 parts by weight of butyl acrylate (BA), 10 parts by weight of acrylic acid (AA), and 2, as a polymerization initiator. 0.2 parts by weight of 2'-azobisisobutyronitrile and 234 parts by weight of ethyl acetate were charged, nitrogen gas was introduced with gentle stirring, and the liquid temperature in the flask was maintained at around 63 ° C. for about 7 hours polymerization. The reaction was carried out to prepare an acrylic polymer (A) solution (30% by weight). The weight average molecular weight of the acrylic polymer (A) was 600,000, and the Tg was −50 ° C. Acrylic polymer (A) solution (30% by weight) is diluted to 20% by weight with ethyl acetate, and an epoxy-based cross-linking agent (Mitsubishi Gas) is used as a cross-linking agent for 100 parts by weight (solid content) of the acrylic polymer in this solution. 11 parts by weight of TETRAD-C) manufactured by Kagaku Co., Ltd. was added, and the mixture was mixed and stirred for about 1 minute at about 25 ° C. to prepare an acrylic pressure-sensitive adhesive composition.
The acrylic pressure-sensitive adhesive composition is applied to one side of a polyethylene terephthalate (PET) base material (thickness 110 μm) and heated at 140 ° C. for 60 seconds to form a pressure-sensitive adhesive layer having a thickness of 20 μm. A thickness of 130 μm) was produced. The heat shrinkage of the obtained protective film was 0.04%.
3.印刷層付フィルム積層体の作製
 基材フィルムとして透明ポリイミドフィルム(KOLON社製、製品名「CPITMC_80」、厚み80μm)を用いた。この基材フィルムをロール搬送しながら、その片面に上記ハードコート層形成用塗布液を塗布して塗布層を形成し、塗布層を透明ポリイミドフィルムとともに90℃で2分間加熱した。次いで、塗布層に高圧水銀ランプを用いて紫外線を積算光量300mJ/cmで照射することによりハードコート層を形成した。形成されたハードコート層の厚みは10μmであった。次いで、基材フィルム/ハードコート層の積層体のハードコート層表面に、上記2.で得られた保護フィルムをロールトゥロールにより積層してフィルム積層体を作製した。得られたフィルム積層体を長尺方向100mmおよび幅方向100mmのサイズに切り出し、その周縁部に黒色インクをグラビア印刷により印刷し、平坦な印刷層(黒色の着色層)を形成した。印刷層の幅は12mm、厚みは10μmであった。このようにして、印刷層付フィルム積層体を作製した。なお、黒色インクの処方は以下のとおりであった:バインダー樹脂(アクリル系樹脂:共栄社化学社製、商品名:ライトアクリレートPE-3A)100部、カーボンブラック100部、粘度調整のための溶媒(メチルエチルケトン:MEK)200部。これらの混合物を、超音波による高分散化処理に供し、拡散性向上を図った。
3. 3. Preparation of film laminate with print layer A transparent polyimide film (manufactured by KOLON, product name "CPITMC_80", thickness 80 μm) was used as a base film. While transporting this base film in a roll, the coating liquid for forming a hard coat layer was applied to one side thereof to form a coating layer, and the coating layer was heated together with a transparent polyimide film at 90 ° C. for 2 minutes. Next, a hard coat layer was formed by irradiating the coating layer with ultraviolet rays using a high-pressure mercury lamp at an integrated light intensity of 300 mJ / cm 2. The thickness of the formed hard coat layer was 10 μm. Next, on the surface of the hard coat layer of the laminate of the base film / hard coat layer, the above 2. The protective film obtained in 1) was laminated by roll-to-roll to prepare a film laminate. The obtained film laminate was cut into sizes of 100 mm in the long direction and 100 mm in the width direction, and black ink was printed on the peripheral edge thereof by gravure printing to form a flat printing layer (black colored layer). The width of the print layer was 12 mm and the thickness was 10 μm. In this way, a film laminate with a print layer was produced. The formulation of the black ink was as follows: 100 parts of binder resin (acrylic resin: manufactured by Kyoeisha Chemical Co., Ltd., trade name: light acrylate PE-3A), 100 parts of carbon black, solvent for adjusting viscosity ( Methyl ethyl ketone: MEK) 200 parts. These mixtures were subjected to a high dispersion treatment by ultrasonic waves to improve diffusivity.
 得られた印刷層付フィルム積層体(実質的には、印刷層)を70℃で60分間乾燥し、最終的な印刷層付フィルム積層体を得た。得られた印刷層付フィルム積層体を上記(3)および(4)の評価に供した。結果を表1に示す。 The obtained film laminate with a print layer (substantially, the print layer) was dried at 70 ° C. for 60 minutes to obtain a final film laminate with a print layer. The obtained film laminate with a print layer was subjected to the evaluations (3) and (4) above. The results are shown in Table 1.
<実施例2>
 乾燥を60℃で50分間行ったこと以外は実施例1と同様にして印刷層付フィルム積層体を得た。得られた印刷層付フィルム積層体を実施例1と同様の評価に供した。結果を表1に示す。
<Example 2>
A film laminate with a print layer was obtained in the same manner as in Example 1 except that the film was dried at 60 ° C. for 50 minutes. The obtained film laminate with a print layer was subjected to the same evaluation as in Example 1. The results are shown in Table 1.
<実施例3>
 乾燥を50℃で40分間行ったこと以外は実施例1と同様にして印刷層付フィルム積層体を得た。得られた印刷層付フィルム積層体を実施例1と同様の評価に供した。結果を表1に示す。
<Example 3>
A film laminate with a print layer was obtained in the same manner as in Example 1 except that the film was dried at 50 ° C. for 40 minutes. The obtained film laminate with a print layer was subjected to the same evaluation as in Example 1. The results are shown in Table 1.
<実施例4>
 乾燥を40℃で30分間行ったこと以外は実施例1と同様にして印刷層付フィルム積層体を得た。得られた印刷層付フィルム積層体を実施例1と同様の評価に供した。結果を表1に示す。
<Example 4>
A film laminate with a print layer was obtained in the same manner as in Example 1 except that the film was dried at 40 ° C. for 30 minutes. The obtained film laminate with a print layer was subjected to the same evaluation as in Example 1. The results are shown in Table 1.
<実施例5>
 基材フィルムを別の透明ポリイミドフィルム(KOLON社製、製品名「CPITMC_50」、厚み50μm)に変更したこと以外は実施例1と同様にして印刷層付フィルム積層体を得た。得られた印刷層付フィルム積層体を実施例1と同様の評価に供した。結果を表1に示す。
<Example 5>
A film laminate with a print layer was obtained in the same manner as in Example 1 except that the base film was changed to another transparent polyimide film (manufactured by KOLON, product name “CPITMC_50”, thickness 50 μm). The obtained film laminate with a print layer was subjected to the same evaluation as in Example 1. The results are shown in Table 1.
<実施例6>
 ハードコート層の厚みを3μmとしたこと以外は実施例1と同様にして印刷層付フィルム積層体を得た。得られた印刷層付フィルム積層体を実施例1と同様の評価に供した。結果を表1に示す。
<Example 6>
A film laminate with a print layer was obtained in the same manner as in Example 1 except that the thickness of the hard coat layer was 3 μm. The obtained film laminate with a print layer was subjected to the same evaluation as in Example 1. The results are shown in Table 1.
<実施例7>
 ハードコート層の厚みを8μmとしたこと以外は実施例1と同様にして印刷層付フィルム積層体を得た。得られた印刷層付フィルム積層体を実施例1と同様の評価に供した。結果を表1に示す。
<Example 7>
A film laminate with a print layer was obtained in the same manner as in Example 1 except that the thickness of the hard coat layer was 8 μm. The obtained film laminate with a print layer was subjected to the same evaluation as in Example 1. The results are shown in Table 1.
<実施例8>
 ハードコート層の厚みを13μmとしたこと以外は実施例1と同様にして印刷層付フィルム積層体を得た。得られた印刷層付フィルム積層体を実施例1と同様の評価に供した。結果を表1に示す。
<Example 8>
A film laminate with a print layer was obtained in the same manner as in Example 1 except that the thickness of the hard coat layer was 13 μm. The obtained film laminate with a print layer was subjected to the same evaluation as in Example 1. The results are shown in Table 1.
<実施例9>
 ハードコート層の厚みを20μmとしたこと以外は実施例1と同様にして印刷層付フィルム積層体を得た。得られた印刷層付フィルム積層体を実施例1と同様の評価に供した。結果を表1に示す。
<Example 9>
A film laminate with a print layer was obtained in the same manner as in Example 1 except that the thickness of the hard coat layer was 20 μm. The obtained film laminate with a print layer was subjected to the same evaluation as in Example 1. The results are shown in Table 1.
<実施例10>
 保護フィルムを別のポリエチレンテレフタレートフィルム(日東電工社製、製品名「IP300F」、厚み38μm、熱収縮率0.07%)に変更したこと以外は実施例1と同様にして印刷層付フィルム積層体を得た。得られた印刷層付フィルム積層体を実施例1と同様の評価に供した。結果を表1に示す。
<Example 10>
A film laminate with a print layer in the same manner as in Example 1 except that the protective film was changed to another polyethylene terephthalate film (manufactured by Nitto Denko Corporation, product name "IP300F", thickness 38 μm, heat shrinkage rate 0.07%). Got The obtained film laminate with a print layer was subjected to the same evaluation as in Example 1. The results are shown in Table 1.
<比較例1>
 保護フィルムをポリエチレンフィルム(東レフィルム加工社製、製品名「トレテック7832C」、厚み30μm、熱収縮率0.87%)に変更したこと以外は実施例1と同様にして印刷層付フィルム積層体を得た。得られた印刷層付フィルム積層体を実施例1と同様の評価に供した。結果を表1に示す。
<Comparative example 1>
A film laminate with a print layer was prepared in the same manner as in Example 1 except that the protective film was changed to a polyethylene film (manufactured by Toray Film Processing Co., Ltd., product name "Tretec 7832C", thickness 30 μm, heat shrinkage rate 0.87%). Obtained. The obtained film laminate with a print layer was subjected to the same evaluation as in Example 1. The results are shown in Table 1.
<比較例2>
 保護フィルムをポリエチレンフィルム(東レフィルム加工社製、製品名「トレテック7832C」、厚み30μm、熱収縮率0.87%)に変更したこと以外は実施例5と同様にして印刷層付フィルム積層体を得た。得られた印刷層付フィルム積層体を実施例1と同様の評価に供した。結果を表1に示す。
<Comparative example 2>
A film laminate with a print layer was prepared in the same manner as in Example 5 except that the protective film was changed to a polyethylene film (manufactured by Toray Film Processing Co., Ltd., product name "Tretec 7832C", thickness 30 μm, heat shrinkage rate 0.87%). Obtained. The obtained film laminate with a print layer was subjected to the same evaluation as in Example 1. The results are shown in Table 1.
<比較例3>
 保護フィルムを積層しなかったこと以外は実施例1と同様にして印刷層付フィルム積層体を得た。得られた印刷層付フィルム積層体を実施例1と同様の評価に供した。結果を表1に示す。
<Comparative example 3>
A film laminate with a print layer was obtained in the same manner as in Example 1 except that the protective film was not laminated. The obtained film laminate with a print layer was subjected to the same evaluation as in Example 1. The results are shown in Table 1.
Figure JPOXMLDOC01-appb-T000001
Figure JPOXMLDOC01-appb-T000001
<評価>
 表1から明らかなように、本発明の実施例の印刷層付フィルム積層体は、高い鉛筆硬度を維持しつつ、反り量(カール)が顕著に抑制されている。
<Evaluation>
As is clear from Table 1, in the film laminate with the printing layer of the embodiment of the present invention, the amount of warpage (curl) is remarkably suppressed while maintaining high pencil hardness.
 本発明の印刷層付フィルム積層体は、画像表示装置のウィンドウフィルムとして好適に用いられ得る。本発明の光学積層体は、画像表示装置の視認側部材として好適に用いられ得る。 The film laminate with a print layer of the present invention can be suitably used as a window film of an image display device. The optical laminate of the present invention can be suitably used as a visible side member of an image display device.
 10   基材フィルム
 20   ハードコート層
 30   印刷層
 40   保護フィルム
100   印刷層付フィルム積層体
120   光学フィルム
200   光学積層体
 
10 Base film 20 Hard coat layer 30 Printing layer 40 Protective film 100 Film laminate with printing layer 120 Optical film 200 Optical laminate

Claims (12)

  1.  基材フィルムの一方の面にハードコート層を形成すること;
     該基材フィルムの他方の面に印刷層を形成すること;
     該ハードコート層の表面に、搬送方向の熱収縮率が0.1%以下である保護フィルムを積層すること;および
     該保護フィルムを積層した状態で該印刷層を加熱乾燥すること、
     を含む、印刷層付フィルム積層体の製造方法。
    Forming a hard coat layer on one side of the substrate film;
    Forming a print layer on the other side of the substrate film;
    Laminating a protective film having a heat shrinkage rate of 0.1% or less in the transport direction on the surface of the hard coat layer; and heating and drying the printed layer with the protective film laminated.
    A method for producing a film laminate with a print layer, including.
  2.  前記印刷層の加熱乾燥が、40℃以上で20分以上行われる、請求項1に記載の製造方法。 The manufacturing method according to claim 1, wherein the printing layer is heat-dried at 40 ° C. or higher for 20 minutes or longer.
  3.  前記保護フィルムが、前記基材フィルムと前記ハードコート層との積層体のハードコート層表面にロールトゥロールにより積層される、請求項1または2に記載の製造方法。 The production method according to claim 1 or 2, wherein the protective film is laminated by roll-to-roll on the surface of the hard coat layer of the laminate of the base film and the hard coat layer.
  4.  前記印刷層が、前記保護フィルムの積層後に形成される、請求項1から3のいずれかに記載の製造方法。 The manufacturing method according to any one of claims 1 to 3, wherein the printing layer is formed after laminating the protective film.
  5.  前記保護フィルムの積層と前記印刷層の形成との間に、前記基材フィルムと前記ハードコート層と該保護フィルムとの積層体を所定サイズおよび所定形状に裁断することをさらに含む、請求項4に記載の製造方法。 4. A claim further comprising cutting a laminate of the base film, the hard coat layer, and the protective film into a predetermined size and a predetermined shape between the lamination of the protective film and the formation of the print layer. The manufacturing method described in.
  6.  前記ハードコート層が、活性エネルギー線硬化型(メタ)アクリレートを含むハードコート層形成用塗布液を塗布して塗布層を形成し、該塗布層に活性エネルギー線を照射して硬化させることにより形成される、請求項1から5のいずれかに記載の製造方法。 The hard coat layer is formed by applying a coating liquid for forming a hard coat layer containing an active energy ray-curable (meth) acrylate to form a coating layer, and irradiating the coating layer with active energy rays to cure the coating layer. The production method according to any one of claims 1 to 5.
  7.  請求項1から6のいずれかに記載の製造方法により得られた印刷層付フィルム積層体の前記基材フィルムの前記ハードコート層と反対側に、光学フィルムを積層することを含む、光学積層体の製造方法。 An optical laminate comprising laminating an optical film on the opposite side of the base film of the film laminate with a print layer obtained by the production method according to any one of claims 1 to 6 to the hard coat layer. Manufacturing method.
  8.  前記光学フィルムを積層した後、前記保護フィルムを剥離することを含む、請求項7に記載の製造方法。 The manufacturing method according to claim 7, which comprises laminating the optical films and then peeling off the protective film.
  9.  画像表示セルの視認側に光学フィルムおよび請求項1から6のいずれかに記載の製造方法により得られた印刷層付フィルム積層体を積層することを含む、画像表示装置の製造方法。 A method for manufacturing an image display device, which comprises laminating an optical film and a film laminate with a print layer obtained by the manufacturing method according to any one of claims 1 to 6 on the visual side of an image display cell.
  10.  前記光学フィルムおよび前記印刷層付フィルム積層体を積層した後、前記保護フィルムを剥離することを含む、請求項9に記載の製造方法。 The manufacturing method according to claim 9, further comprising peeling off the protective film after laminating the optical film and the film laminate with the print layer.
  11.  画像表示セルの視認側に請求項7または8に記載の製造方法により得られた光学積層体を積層することを含む、画像表示装置の製造方法。 A method for manufacturing an image display device, which comprises laminating an optical laminate obtained by the manufacturing method according to claim 7 or 8 on the visual side of an image display cell.
  12.  前記光学積層体を積層した後、前記保護フィルムを剥離することを含む、請求項11に記載の製造方法。 The manufacturing method according to claim 11, further comprising peeling off the protective film after laminating the optical laminate.
PCT/JP2020/024374 2019-10-07 2020-06-22 Method for manufacturing film laminate having print layer WO2021070425A1 (en)

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