WO2020189146A1 - Corps multicouche et dispositif d'affichage le comprenant - Google Patents

Corps multicouche et dispositif d'affichage le comprenant Download PDF

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Publication number
WO2020189146A1
WO2020189146A1 PCT/JP2020/006272 JP2020006272W WO2020189146A1 WO 2020189146 A1 WO2020189146 A1 WO 2020189146A1 JP 2020006272 W JP2020006272 W JP 2020006272W WO 2020189146 A1 WO2020189146 A1 WO 2020189146A1
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Prior art keywords
pressure
sensitive adhesive
layer
thickness
adhesive composition
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PCT/JP2020/006272
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English (en)
Japanese (ja)
Inventor
昇祐 李
正熙 金
Original Assignee
住友化学株式会社
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Priority to CN202080021500.7A priority Critical patent/CN113614589B/zh
Priority to KR1020217030611A priority patent/KR20210141521A/ko
Publication of WO2020189146A1 publication Critical patent/WO2020189146A1/fr

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    • G—PHYSICS
    • G02—OPTICS
    • G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B5/00—Optical elements other than lenses
    • G02B5/30—Polarising elements
    • G02B5/3025—Polarisers, i.e. arrangements capable of producing a definite output polarisation state from an unpolarised input state
    • G02B5/3033—Polarisers, i.e. arrangements capable of producing a definite output polarisation state from an unpolarised input state in the form of a thin sheet or foil, e.g. Polaroid
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K59/00—Integrated devices, or assemblies of multiple devices, comprising at least one organic light-emitting element covered by group H10K50/00
    • H10K59/80—Constructional details
    • H10K59/8791—Arrangements for improving contrast, e.g. preventing reflection of ambient light
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B7/00—Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
    • B32B7/02—Physical, chemical or physicochemical properties
    • B32B7/022—Mechanical properties
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B7/00—Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
    • B32B7/02—Physical, chemical or physicochemical properties
    • B32B7/023—Optical properties
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B7/00—Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
    • B32B7/04—Interconnection of layers
    • B32B7/12—Interconnection of layers using interposed adhesives or interposed materials with bonding properties
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J7/00—Adhesives in the form of films or foils
    • C09J7/30—Adhesives in the form of films or foils characterised by the adhesive composition
    • C09J7/38—Pressure-sensitive adhesives [PSA]
    • G—PHYSICS
    • G02—OPTICS
    • G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B5/00—Optical elements other than lenses
    • G02B5/30—Polarising elements
    • G—PHYSICS
    • G02—OPTICS
    • G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B5/00—Optical elements other than lenses
    • G02B5/30—Polarising elements
    • G02B5/3083—Birefringent or phase retarding elements
    • G—PHYSICS
    • G02—OPTICS
    • G02F—OPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
    • G02F1/00—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
    • G02F1/01—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour 
    • G02F1/13—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour  based on liquid crystals, e.g. single liquid crystal display cells
    • G02F1/133—Constructional arrangements; Operation of liquid crystal cells; Circuit arrangements
    • G02F1/1333—Constructional arrangements; Manufacturing methods
    • G—PHYSICS
    • G02—OPTICS
    • G02F—OPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
    • G02F1/00—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
    • G02F1/01—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour 
    • G02F1/13—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour  based on liquid crystals, e.g. single liquid crystal display cells
    • G02F1/133—Constructional arrangements; Operation of liquid crystal cells; Circuit arrangements
    • G02F1/1333—Constructional arrangements; Manufacturing methods
    • G02F1/1335—Structural association of cells with optical devices, e.g. polarisers or reflectors
    • G—PHYSICS
    • G02—OPTICS
    • G02F—OPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
    • G02F1/00—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
    • G02F1/01—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour 
    • G02F1/13—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour  based on liquid crystals, e.g. single liquid crystal display cells
    • G02F1/133—Constructional arrangements; Operation of liquid crystal cells; Circuit arrangements
    • G02F1/1333—Constructional arrangements; Manufacturing methods
    • G02F1/1335—Structural association of cells with optical devices, e.g. polarisers or reflectors
    • G02F1/133528—Polarisers
    • G—PHYSICS
    • G06—COMPUTING; CALCULATING OR COUNTING
    • G06F—ELECTRIC DIGITAL DATA PROCESSING
    • G06F3/00—Input arrangements for transferring data to be processed into a form capable of being handled by the computer; Output arrangements for transferring data from processing unit to output unit, e.g. interface arrangements
    • G06F3/01—Input arrangements or combined input and output arrangements for interaction between user and computer
    • G06F3/03—Arrangements for converting the position or the displacement of a member into a coded form
    • G06F3/041—Digitisers, e.g. for touch screens or touch pads, characterised by the transducing means
    • G—PHYSICS
    • G09—EDUCATION; CRYPTOGRAPHY; DISPLAY; ADVERTISING; SEALS
    • G09F—DISPLAYING; ADVERTISING; SIGNS; LABELS OR NAME-PLATES; SEALS
    • G09F9/00—Indicating arrangements for variable information in which the information is built-up on a support by selection or combination of individual elements
    • H—ELECTRICITY
    • H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
    • H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
    • H05B33/00—Electroluminescent light sources
    • H05B33/02—Details
    • H—ELECTRICITY
    • H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
    • H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
    • H05B33/00—Electroluminescent light sources
    • H05B33/12—Light sources with substantially two-dimensional radiating surfaces
    • H05B33/14—Light sources with substantially two-dimensional radiating surfaces characterised by the chemical or physical composition or the arrangement of the electroluminescent material, or by the simultaneous addition of the electroluminescent material in or onto the light source
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K59/00—Integrated devices, or assemblies of multiple devices, comprising at least one organic light-emitting element covered by group H10K50/00
    • H10K59/50—OLEDs integrated with light modulating elements, e.g. with electrochromic elements, photochromic elements or liquid crystal elements

Definitions

  • the present invention relates to a laminate and a display device including the laminate.
  • Korean Patent No. 10-2016-0053788 (Patent Document 1) and Korean Patent No. 10-2017-093610 (Patent Document 2) each include a laminate for a display device having a plurality of pressure-sensitive adhesive layers. Are listed.
  • the adhesive layer used in this type of laminate is generally excellent in stress relaxation performance for relieving external stress.
  • bubbles are often generated in the pressure-sensitive adhesive layer, so that it is required to improve the durability of the pressure-sensitive adhesive layer.
  • an object of the present invention is to provide a laminate having improved durability by suppressing the generation of air bubbles in the pressure-sensitive adhesive layer and a display device containing the same.
  • the present invention provides the following laminate and a display device including the following.
  • the first pressure-sensitive adhesive composition is used to form the first pressure-sensitive adhesive reference layer so that the thickness of the first pressure-sensitive adhesive reference layer and the thickness of the second pressure-sensitive adhesive reference layer are the same.
  • the second pressure-sensitive adhesive reference layer is formed by using the composition, the first pressure-sensitive adhesive reference layer and the second pressure-sensitive adhesive reference layer satisfy the relationship of the following formula (1).
  • ⁇ R1 represents the value obtained by subtracting R1B from R1A.
  • ⁇ R2 represents the value obtained by subtracting R2B from R2A.
  • the R1A represents a first shear creep rate (% / ⁇ m) which is a shear creep value per 1 ⁇ m of thickness at 25 ° C. obtained for the first pressure-sensitive adhesive reference layer after performing a strain repeated addition test.
  • the R1B represents a second shear creep rate (% / ⁇ m), which is a shear creep value per 1 ⁇ m of thickness at 25 ° C. obtained with respect to the first pressure-sensitive adhesive reference layer before executing the strain repeated addition test.
  • the R2A indicates a third shear creep rate (% / ⁇ m), which is a shear creep value per 1 ⁇ m of thickness at 25 ° C. obtained for the second pressure-sensitive adhesive reference layer after performing a strain repeated addition test.
  • the R2B represents a fourth shear creep rate (% / ⁇ m), which is a shear creep value per 1 ⁇ m of thickness obtained at 25 ° C. with respect to the second pressure-sensitive adhesive reference layer before executing the strain repeated addition test.
  • [2] The laminate according to [1], wherein the fourth shear creep rate (% / ⁇ m) is 0.1 or more and 0.2 or less.
  • the present invention it is possible to provide a laminate having improved durability by suppressing the generation of air bubbles in the pressure-sensitive adhesive layer and a display device containing the same.
  • laminated body according to one aspect of the present invention (hereinafter, also simply referred to as “laminated body”) will be described with reference to the drawings.
  • FIG. 1 shows a schematic cross-sectional view of the laminated body according to one aspect of the present invention.
  • the laminate 100 is formed by using the front plate 101, the first pressure-sensitive adhesive layer 102 formed by using the first pressure-sensitive adhesive composition, the polarizer layer 103, and the second pressure-sensitive adhesive composition.
  • the pressure-sensitive adhesive layer 104 and the back plate 105 are included in this order.
  • the first pressure-sensitive adhesive layer 102 and the second pressure-sensitive adhesive layer 104 may be generically referred to as a “pressure-sensitive adhesive layer”.
  • the thickness of the laminated body 100 is not particularly limited because it varies depending on the function required for the laminated body, the application of the laminated body, etc. It is 500 ⁇ m or less.
  • the plan view shape of the laminated body 100 may be, for example, a rectangular shape, preferably a rectangular shape having a long side and a short side, and more preferably a rectangular shape.
  • the length of the long side may be, for example, 10 mm or more and 1400 mm or less, preferably 50 mm or more and 600 mm or less.
  • the length of the short side may be, for example, 5 mm or more and 800 mm or less, preferably 30 mm or more and 500 mm or less, and more preferably 50 mm or more and 300 mm or less.
  • Each layer constituting the laminate may have corners R-processed, end portions notched, or perforated.
  • the laminated body 100 can be applied to, for example, a display device or the like.
  • the display device is not particularly limited, and examples thereof include an organic electroluminescence (organic EL) display device, an inorganic electroluminescence (inorganic EL) display device, a liquid crystal display device, and an electroluminescent display device.
  • the display device may have a touch panel function.
  • the display device to which the laminated body 100 is applied can be used as a flexible display that can be bent or wound.
  • the display device is preferably bendable with the front plate 101 side facing outward. However, the laminated body 100 may be able to be bent with the front plate 101 side inside.
  • the laminate 100 includes a first pressure-sensitive adhesive layer 102 formed by using the first pressure-sensitive adhesive composition as described above, and a second pressure-sensitive adhesive layer 104 formed by using the second pressure-sensitive adhesive composition. .. In the laminate 100, between the first pressure-sensitive adhesive composition used for forming the first pressure-sensitive adhesive layer 102 and the second pressure-sensitive adhesive composition used for forming the second pressure-sensitive adhesive layer 104, The following relationships are built.
  • the first pressure-sensitive adhesive reference layer is formed using the first pressure-sensitive adhesive composition so that the thickness of the first pressure-sensitive adhesive reference layer and the thickness of the second pressure-sensitive adhesive reference layer are the same, and the second pressure-sensitive adhesive reference layer is formed.
  • the first pressure-sensitive adhesive reference layer and the second pressure-sensitive adhesive reference layer satisfy the relationship of the following formula (1).
  • the thickness of the first pressure-sensitive adhesive reference layer and the thickness of the second pressure-sensitive adhesive reference layer can be, for example, 200 ⁇ m.
  • ⁇ R1 represents the value obtained by subtracting R1B from R1A.
  • ⁇ R2 represents the value obtained by subtracting R2B from R2A.
  • R1A represents the first shear creep rate (% / ⁇ m), which is the shear creep value per 1 ⁇ m of thickness at 25 ° C., which was obtained for the first pressure-sensitive adhesive reference layer after performing the strain repeated addition test.
  • R1B represents the second shear creep rate (% / ⁇ m), which is the shear creep value per 1 ⁇ m of thickness at 25 ° C., which was obtained for the first pressure-sensitive adhesive reference layer before performing the strain repeated addition test.
  • R2A indicates a third shear creep rate (% / ⁇ m), which is a shear creep value per 1 ⁇ m of thickness at 25 ° C., which was obtained for the second pressure-sensitive adhesive reference layer after performing the strain repeated addition test.
  • R2B represents the fourth shear creep rate (% / ⁇ m), which is the shear creep value per 1 ⁇ m of thickness at 25 ° C., which was obtained for the second pressure-sensitive adhesive reference layer before the strain repeated addition test was performed. ].
  • the fourth shear creep rate (% / ⁇ m) representing (/ ⁇ m) and R2B can be determined according to the measurement methods described in the columns of Examples described later, respectively.
  • the first pressure-sensitive adhesive layer 102 and the second pressure-sensitive adhesive layer 104 which are the pressure-sensitive adhesive layers contained therein, are the first pressure-sensitive adhesive reference layer and the second pressure-sensitive adhesive standard that satisfy the relationship of the above formula (1). It is formed by using a first pressure-sensitive adhesive composition and a second pressure-sensitive adhesive composition that can form a layer.
  • the laminate 100 can improve the durability by suppressing the generation of air bubbles in the pressure-sensitive adhesive layer.
  • the laminated body 100 is preferably used for a laminated body of a method (so-called outfolding method) in which the front plate side is turned outward and a display device including the laminated body 100.
  • the reason why the above-mentioned effects are obtained when each of the pressure-sensitive adhesive compositions is formed is not clear in detail, but is considered to be due to the following mechanism.
  • the second pressure-sensitive adhesive composition is repeatedly strained as compared with the first pressure-sensitive adhesive composition. It means that the composition has a smaller change in shear creep rate (% / ⁇ m) before and after being added. Furthermore, the feature that the change in shear creep rate (% / ⁇ m) is small is that it is excellent in performance (that is, durability) that can maintain the properties peculiar to the pressure-sensitive adhesive layer against external stress. means. Therefore, the pressure-sensitive adhesive layer (second pressure-sensitive adhesive layer 104) formed by using the second pressure-sensitive adhesive composition is formed on the pressure-sensitive adhesive layer (first pressure-sensitive adhesive layer 102) formed by using the first pressure-sensitive adhesive composition. In comparison, it is considered that the durability against bending can be improved.
  • the present inventors have a second pressure-sensitive adhesive composition that is more durable against bending as a pressure-sensitive adhesive layer on the side far from the front plate where bubbles frequently occur when the laminate is bent with the front plate side on the outside.
  • a pressure-sensitive adhesive layer (second pressure-sensitive adhesive layer 104) formed by using an object was arranged.
  • the laminated body 100 is bent with the front plate 101 side facing outward, the laminated body 100 is reached, which can suppress the generation of air bubbles in the pressure-sensitive adhesive layer.
  • the laminate 100 has a mandrel (mandrel), which is a cylindrical jig having a diameter ( ⁇ ) of more than 10 mm and a diameter of 15 mm or less, arranged inside the back plate 105 side. Even when the laminate 100 is bent along the mandrel, the generation of air bubbles in the pressure-sensitive adhesive layer can be suppressed (hereinafter, such performance is also referred to as "excellent bending durability"). ..
  • bending includes a form of bending in which a curved surface is formed in the bent portion.
  • the radius of curvature of the bent inner surface is not limited unless otherwise specified.
  • bending includes a form of refraction in which the refraction angle of the inner surface is larger than 0 degrees and less than 180 degrees unless otherwise specified, and the radius of curvature of the inner surface is close to zero, or the refraction angle of the inner surface is 0 degrees. Includes certain forms of folding.
  • ⁇ R1 and ⁇ R2 are preferably 0.01 to 4, more preferably 0.05 to 0.5, and even more preferably 0.05 to 0.2, respectively.
  • the first shear creep rate R1A (% / ⁇ m) is preferably 0.05 to 1.0, and more preferably 0.2 to 0.5.
  • the second shear creep rate R1B (% / ⁇ m) is preferably 0.01 to 0.3, and more preferably 0.05 to 0.2.
  • the third shear creep ratio R2A (% / ⁇ m) is preferably 0.05 to 1.0, and more preferably 0.2 to 0.5.
  • the fourth shear creep ratio R2B (% / ⁇ m) is preferably 0.01 to 0.3, and more preferably 0.05 to 0.2.
  • the fourth shear creep rate (% / ⁇ m) is preferably 0.1 or more and 0.2 or less.
  • the second pressure-sensitive adhesive layer 104 is a pressure-sensitive adhesive layer having not only excellent flexibility and durability but also appropriate hardness, it is possible to impart excellent surface hardness to the laminate 100.
  • a load of 100 g is applied to the surface of the back plate 105 of the laminate 100 using a pencil having a core hardness of 6B, the surface is subjected to a load of 100 g.
  • the formed recess marks can be eliminated in less than one hour (hereinafter, such performance is also referred to as "excellent in” surface hardness ").
  • the gel fraction of the pressure-sensitive adhesive layer can be 40 to 90% and may be 50 to 80%.
  • the gel fraction of the pressure-sensitive adhesive layer is measured by the method described in Examples below.
  • At least one of the first pressure-sensitive adhesive layer 102 and the second pressure-sensitive adhesive layer 104 preferably has a thickness of 20 ⁇ m or more and 50 ⁇ m or less.
  • the first pressure-sensitive adhesive composition and the second pressure-sensitive adhesive composition constituting the first pressure-sensitive adhesive reference layer and the second pressure-sensitive adhesive reference layer satisfying the relationship of the above formula (1) are used.
  • a method of forming the pressure-sensitive adhesive composition A described later, changing the type of the monomer constituting the (meth) acrylic polymer A described later, adjusting the molecular weight of the (meth) acrylic polymer A, etc. can be mentioned.
  • the pressure-sensitive adhesive composition A will be specifically described.
  • the pressure-sensitive adhesive composition A may be an active energy ray-curable type or a thermosetting type.
  • (meth) acrylic polymer refers to at least one selected from the group consisting of acrylic polymers and methacrylic polymers. The same applies to other terms with "(meta)”.
  • both the first pressure-sensitive adhesive composition and the second pressure-sensitive adhesive composition contain a (meth) acrylic polymer
  • the (meth) acrylic polymer may be the same or different.
  • the (meth) acrylic polymer contained in the pressure-sensitive adhesive composition A is also referred to as “(meth) acrylic polymer A”.
  • the (meth) acrylic polymer A contained in the pressure-sensitive adhesive composition A has a structural unit derived from a monomer having a reactive functional group. Preferably, it is 1% by mass or less based on the total mass of the polymer.
  • the reactive functional group include a hydroxyl group, a carboxyl group, an amino group, an amide group, an epoxy group and the like.
  • the structural unit derived from the monomer having a reactive functional group is more preferably 0.01% by mass based on the total mass of the polymer from the viewpoint of suppressing the generation of bubbles at the time of bending. It is more preferably free of structural units derived from monomers having reactive functional groups, and even more preferably free of hydroxyl groups, carboxyl groups, amino groups, amide groups, and epoxy groups.
  • the (meth) acrylic polymer A can contain a structural unit derived from a (meth) acrylic monomer having a linear or branched chain-like alkyl group having 1 to 24 carbon atoms.
  • the (meth) acrylic monomer having an alkyl group having 1 or more and 24 or less carbon atoms in a linear or branched chain may be, for example, a (meth) acrylic acid alkyl ester, and an example thereof is (meth).
  • the (meth) acrylic polymer A may be a polymer or a copolymer containing one or more of the above (meth) acrylic acid alkyl esters as monomers.
  • the content of the (meth) acrylic polymer A in the pressure-sensitive adhesive composition A may be, for example, 50% by mass or more and 100% by mass or less, preferably 80% by mass or less, based on 100 parts by mass of the solid content of the pressure-sensitive adhesive composition A. It is by mass% or more and 99.5% by mass or less, and more preferably 90% by mass or more and 99% by mass or less.
  • the weight average molecular weight (Mw) of the (meth) acrylic polymer A may be, for example, 100,000 or more and 2 million or less, and preferably 500,000 or more and 1.5 million or less from the viewpoint of suppressing air bubbles at the time of bending.
  • the weight average molecular weight in the present specification can be determined based on a standard polystyrene-equivalent value measured by a gel permeation chromatography (GPC) method, as described in the column of Examples described later.
  • the pressure-sensitive adhesive composition A may contain one or more (meth) acrylic polymers A. Further, the pressure-sensitive adhesive composition A may contain only the (meth) acrylic polymer A as a constituent component thereof, or may further contain a cross-linking agent.
  • the cross-linking agent is a divalent or higher metal ion that forms a carboxylic acid metal salt with a carboxyl group; a polyamine compound that forms an amide bond with a carboxyl group; poly. Examples include epoxy compounds or polyols that form an ester bond with a carboxyl group; polyisocyanate compounds that form an amide bond with a carboxyl group, and the like. Of these, polyisocyanate compounds are preferable.
  • the content of the cross-linking agent may be, for example, 5 parts by mass or less, preferably 3 parts by mass or less, based on 100 parts by mass of the (meth) acrylic polymer A. It is preferably 1 part by mass or less, more preferably 0.5 part by mass or less.
  • the pressure-sensitive adhesive composition A may not contain a cross-linking agent.
  • the active energy ray-curable pressure-sensitive adhesive composition has a property of being cured by being irradiated with active energy rays such as ultraviolet rays or electron beams, and has adhesiveness even before irradiation with active energy rays. It is a pressure-sensitive adhesive composition having the property of being able to adhere to an adherend such as, etc., and being cured by irradiation with active energy rays to adjust the adhesion force and the like.
  • the active energy ray-curable pressure-sensitive adhesive composition is preferably an ultraviolet-curable type.
  • the pressure-sensitive adhesive composition A is an active energy ray-curable pressure-sensitive adhesive composition
  • the pressure-sensitive adhesive composition A can further contain an active energy ray-polymerizable compound, a photopolymerization initiator, a photosensitizer, and the like. ..
  • the active energy ray-polymerizable compound is, for example, a (meth) acrylate monomer having at least one (meth) acryloyloxy group in the molecule; obtained by reacting two or more kinds of functional group-containing compounds, and at least in the molecule.
  • Examples thereof include (meth) acrylic compounds such as (meth) acryloyloxy group-containing compounds such as (meth) acrylate oligomers having two (meth) acryloyloxy groups.
  • the pressure-sensitive adhesive composition A can contain an active energy ray-polymerizable compound in an amount of 0.1 part by mass or more and 10 parts by mass or less with respect to 100 parts by mass of the solid content of the pressure-sensitive adhesive composition A.
  • the photopolymerization initiator examples include benzophenone, benzyl dimethyl ketal, 1-hydroxycyclohexyl ketone and the like.
  • the pressure-sensitive adhesive composition A may contain one or more.
  • the pressure-sensitive adhesive composition A contains a photopolymerization initiator, the total content thereof may be, for example, 0.01 part by mass or more and 1.0 part by mass or less with respect to 100 parts by mass of the solid content of the pressure-sensitive adhesive composition A. ..
  • the pressure-sensitive adhesive composition A contains fine particles, beads (resin beads, glass beads, etc.), glass fibers, resins other than the base polymer, a pressure-sensitive imparting agent, and a filler (metal powder or other inorganic substances) for imparting light scattering properties. Additives such as powders), antioxidants, UV absorbers, dyes, pigments, colorants, antifoaming agents, corrosion inhibitors, etc. can be included.
  • the pressure-sensitive adhesive composition A preferably does not contain an organic solvent from the viewpoint of preventing the problem of deterioration of durability due to the residual solvent.
  • the pressure-sensitive adhesive layer When the pressure-sensitive adhesive layer is formed from the pressure-sensitive adhesive composition A, the pressure-sensitive adhesive layer can be formed by applying the pressure-sensitive adhesive composition A on a substrate.
  • the formed pressure-sensitive adhesive layer can be irradiated with active energy rays to obtain a cured product having a desired degree of curing.
  • the (meth) acrylic polymer A is a (meth) acrylic having an alkyl group having 2 to 20 carbon atoms as a monomer unit constituting the polymer. It is preferable to contain an acid alkyl ester and a monomer having a reactive functional group in the molecule (reactive functional group-containing monomer).
  • the pressure-sensitive adhesive composition A is a thermosetting pressure-sensitive adhesive composition, it preferably further contains a heat-crosslinking agent.
  • the (meth) acrylic polymer A can exhibit preferable tackiness by containing a (meth) acrylic acid alkyl ester having an alkyl group having 2 to 20 carbon atoms as a monomer unit constituting the polymer. it can.
  • the (meth) acrylic acid alkyl ester having an alkyl group having 2 to 20 carbon atoms is, for example, a homopolymer having a glass transition temperature (Tg) of ⁇ 40 ° C. or lower (hereinafter, may be referred to as “low Tg alkyl acrylate”). It is preferable to include it.
  • the glass transition temperature (Tg) of the (meth) acrylic polymer A can be determined by using a conventionally known method such as differential thermal analysis (DTA).
  • Examples of the low Tg alkyl acrylate include n-butyl acrylate (Tg-54 ° C.), n-octyl acrylate (Tg-65 ° C.), isooctyl acrylate (Tg-58 ° C.), and 2-ethylhexyl acrylate (Tg).
  • the Tg of the homopolymer is more preferably ⁇ 45 ° C. or lower, and particularly preferably ⁇ 50 ° C. or lower.
  • n-butyl acrylate and 2-ethylhexyl acrylate are particularly preferable. These may be used alone or in combination of two or more.
  • the (meth) acrylic polymer A preferably contains low Tg alkyl acrylate as a lower limit value of 85% by mass or more, more preferably 90% by mass or more, as a monomer unit constituting the polymer. It is more preferably contained in an amount of mass% or more.
  • the (meth) acrylic polymer A preferably contains the above-mentioned low Tg alkyl acrylate as a monomer unit constituting the polymer in an upper limit of 99.9% by mass or less, and preferably 99.5% by mass or less. Is more preferable, and it is further preferable that the content is 99% by mass or less.
  • a suitable amount of other monomer components can be introduced into the (meth) acrylic polymer A.
  • the (meth) acrylic polymer A is a monomer having a glass transition temperature (Tg) of more than 0 ° C. as a homopolymer (hereinafter, may be referred to as “hard monomer”) from the viewpoint of further exerting the effect of the present invention. It is preferable to reduce the content as much as possible.
  • the (meth) acrylic polymer A preferably has a hard monomer content of 15% by mass or less as an upper limit as a monomer unit constituting the polymer, and is preferably 10% by mass or less. More preferably, it is more preferably 5% by mass or less.
  • This hard monomer also includes a reactive functional group-containing monomer described later.
  • Examples of the hard monomer include methyl acrylate (Tg10 ° C.), methyl methacrylate (Tg105 ° C.), ethyl methacrylate (Tg65 ° C.), n-butyl methacrylate (Tg20 ° C.), isobutyl methacrylate (Tg48 ° C.), and the like.
  • T-butyl methacrylate (Tg 107 ° C), n-stearyl acrylate (Tg 30 ° C), n-stearyl methacrylate (Tg 38 ° C), cyclohexyl acrylate (Tg 15 ° C), cyclohexyl methacrylate (Tg 66 ° C), phenoxyethyl acrylate (Tg 5 ° C), phenoxyethyl methacrylate (Tg 54 ° C), benzyl methacrylate (Tg 54 ° C), isobornyl acrylate (Tg 94 ° C), isobornyl methacrylate (Tg 180 ° C), acryloylmorpholin (Tg 145 ° C), adamantyl acrylate (Tg115 ° C).
  • Tg141 °C adamantyl methacrylate
  • acrylic acid Tg105 °C
  • dimethylacrylamide Tg89 °C
  • acrylamide Tg165 °C
  • other acrylic monomers vinyl acetate (Tg32 °C)
  • styrene Tg80 °C
  • the (meth) acrylic polymer A contains a reactive functional group-containing monomer as a monomer unit constituting the polymer, and thus heats described later via the reactive functional group derived from the reactive functional group-containing monomer. Reacts with cross-linking agents. As a result, a crosslinked structure (three-dimensional network structure) is formed as a whole, and a pressure-sensitive adhesive having a desired cohesive force can be obtained.
  • Examples of the reactive functional group-containing monomer contained in the (meth) acrylic polymer A as a monomer unit constituting the polymer include a monomer having a hydroxyl group in the molecule (monomer containing a hydroxyl group) and a monomer having a carboxy group in the molecule.
  • (Carboxy group-containing monomer), a monomer having an amino group in the molecule (amino group-containing monomer), and the like are preferably mentioned.
  • hydroxyl group-containing monomers are particularly preferable because many of them have a glass transition temperature (Tg) of 0 ° C. or lower.
  • hydroxyl group-containing monomer examples include 2-hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate, 3-hydroxypropyl (meth) acrylate, 2-hydroxybutyl (meth) acrylate, and (meth).
  • Hydroxyalkyl esters of (meth) acrylates such as 3-hydroxybutyl acrylate and 4-hydroxybutyl (meth) acrylate can be mentioned.
  • 2-hydroxyethyl acrylate is obtained from the viewpoints of glass transition temperature (Tg), reactivity of hydroxyl group in the obtained (meth) acrylic polymer A with a thermal cross-linking agent, and copolymerizability with other monomers.
  • Tg glass transition temperature
  • 2-Hydroxypropyl acrylate, 3-hydroxypropyl acrylate, and 4-hydroxybutyl acrylate are preferred. These may be used alone or in combination of two or more.
  • carboxy group-containing monomer examples include ethylenically unsaturated carboxylic acids such as acrylic acid, methacrylic acid, crotonic acid, maleic acid, itaconic acid, and citraconic acid. These may be used alone or in combination of two or more.
  • carboxylic acids such as acrylic acid, methacrylic acid, crotonic acid, maleic acid, itaconic acid, and citraconic acid. These may be used alone or in combination of two or more.
  • amino group-containing monomer examples include aminoethyl (meth) acrylate and n-butylaminoethyl (meth) acrylate. These may be used alone or in combination of two or more.
  • the (meth) acrylic polymer A preferably contains a reactive functional group-containing monomer as a lower limit value of 0.1% by mass or more, and particularly 0.5% by mass or more, as a monomer unit constituting the polymer. It is preferable that the content is 1% by mass or more.
  • the (meth) acrylic polymer A preferably contains the above-mentioned reactive functional group-containing monomer as an upper limit value of 10% by mass or less, particularly preferably 8% by mass or less, and further contains 5% by mass or less. Is preferable. This tends to make it easier to suppress the generation of air bubbles during bending.
  • the (meth) acrylic polymer A may not contain a carboxy group-containing monomer, particularly acrylic acid, which is also a hard monomer, as a monomer unit constituting the polymer. Since the carboxy group is an acid component, a transparent conductive film such as tin-doped indium oxide (ITO), a metal film, or a metal that causes problems due to the acid on the object to which the pressure-sensitive adhesive is applied because the carboxy group-containing monomer is not contained. Even when a mesh or the like is present, those defects (corrosion, change in resistance value, etc.) due to acid can be suppressed.
  • a carboxy group-containing monomer particularly acrylic acid, which is also a hard monomer, as a monomer unit constituting the polymer. Since the carboxy group is an acid component, a transparent conductive film such as tin-doped indium oxide (ITO), a metal film, or a metal that causes problems due to the acid on the object to which the pressure-sensitive adhesive is applied because the carboxy
  • the (meth) acrylic polymer A may contain another monomer as a monomer unit constituting the polymer.
  • a monomer containing no reactive functional group is preferable so as not to interfere with the action of the reactive functional group-containing monomer.
  • the other monomers include (meth) acrylic acid alkoxyalkyl esters such as methoxyethyl (meth) acrylate and ethoxyethyl (meth) acrylate, as well as a glass transition temperature (Tg) of -40 as a homopolymer.
  • Tg glass transition temperature
  • examples thereof include a monomer having a temperature exceeding 0 ° C. or lower (hereinafter, may be referred to as “medium Tg alkyl acrylate”).
  • Examples of the medium Tg alkyl acrylate include ethyl acrylate (Tg-20 ° C.), isobutyl acrylate (Tg-26 ° C.), 2-ethylhexyl methacrylate (Tg-10 ° C.), and n-lauryl acrylate (Tg-23 ° C.). ° C.), isostearyl acrylate (Tg-18 ° C.) and the like. These may be used alone or in combination of two or more.
  • the polymerization mode of the (meth) acrylic polymer A may be a random copolymer or a block copolymer.
  • the lower limit of the weight average molecular weight of the (meth) acrylic polymer A is preferably 200,000 or more, particularly preferably 300,000 or more, and further preferably 400,000 or more.
  • the weight average molecular weight in the present specification can be determined based on a standard polystyrene-equivalent value measured by a gel permeation chromatography (GPC) method, as described in the column of Examples described later.
  • the upper limit of the weight average molecular weight of the (meth) acrylic polymer A is preferably 2 million or less, particularly preferably 1.5 million or less, and further preferably 1.3 million or less.
  • the upper limit of the weight average molecular weight of the (meth) acrylic acid ester polymer (A) is not more than the above, the flexibility of the pressure-sensitive adhesive layer can be ensured, and the effect of the present invention can be easily exhibited. ..
  • one type of (meth) acrylic polymer A may be used alone, or two or more types may be used in combination.
  • the heat-crosslinking agent cross-links the (meth) acrylic polymer A to form a three-dimensional network structure.
  • the cohesive force can be improved while ensuring the flexibility of the pressure-sensitive adhesive, and when applied to the laminated body, it is possible to obtain a hardness capable of improving the surface hardness of the laminated body.
  • the thermal cross-linking agent may be any as long as it reacts with the reactive group of the (meth) acrylic polymer A.
  • an isocyanate-based cross-linking agent an epoxy-based cross-linking agent, an amine-based cross-linking agent, a melamine-based cross-linking agent, and the like.
  • examples thereof include aziridine-based cross-linking agent, hydrazine-based cross-linking agent, aldehyde-based cross-linking agent, oxazoline-based cross-linking agent, metal alkoxide-based cross-linking agent, metal chelate-based cross-linking agent, metal salt-based cross-linking agent, ammonium salt-based cross-linking agent and the like.
  • the reactive group of the (meth) acrylic polymer A is a hydroxyl group
  • an isocyanate-based cross-linking agent having excellent reactivity with the hydroxyl group.
  • the thermal cross-linking agent may be used alone or in combination of two or more.
  • the isocyanate-based cross-linking agent contains at least a polyisocyanate compound.
  • the polyisocyanate compound include aromatic polyisocyanates such as tolylene diisocyanate, diphenylmethane diisocyanate, and xylylene diisocyanate, aliphatic polyisocyanates such as hexamethylene diisocyanate, isophorone diisocyanates, and alicyclic polyisocyanates such as hydrogenated diphenylmethane diisocyanate.
  • trimethylolpropane-modified aromatic polyisocyanates particularly trimethylolpropane-modified tolylene diisocyanate and trimethylolpropane-modified xylylene diisocyanate, are preferable from the viewpoint of reactivity with hydroxyl groups.
  • epoxy-based cross-linking agent examples include 1,3-bis (N, N-diglycidyl aminomethyl) cyclohexane, N, N, N', N'-tetraglycidyl-m-xylylenediamine, and ethylene glycol diglycidyl ether. , 1,6-Hexanediol diglycidyl ether, trimethylpropan diglycidyl ether, diglycidyl aniline, diglycidyl amine and the like.
  • the content of the heat-crosslinking agent in the pressure-sensitive adhesive composition A is preferably 0.01% by mass or more, and preferably 0.05% by mass or more, based on 100% by mass of the (meth) acrylic polymer A. More preferably, it is 0.1% by mass or more. Further, the content is preferably 1% by mass or less, more preferably 0.8% by mass or less, and further preferably 0.5% by mass or less. When the content of the thermal cross-linking agent is in the above range, it is possible to more easily obtain an appropriate hardness by improving the cohesive force.
  • the pressure-sensitive adhesive composition A preferably contains the above-mentioned silane coupling agent.
  • the obtained pressure-sensitive adhesive layer has improved adhesion to each member in the laminated body as an adherend, and has more excellent durability against bending.
  • the silane coupling (SC) agent is preferably an organosilicon compound having at least one alkoxysilyl group in the molecule, which has good compatibility with the (meth) acrylic polymer A and has light transmittance. ..
  • silane coupling agent examples include polymerizable unsaturated group-containing silicon compounds such as vinyltrimethoxysilane, vinyltriethoxysilane, and methacrypropyltrimethoxysilane, 3-glycidoxypropyltrimethoxysilane, and 2- (3).
  • the content of the silane coupling agent in the pressure-sensitive adhesive composition A is preferably 0.01% by mass or more, preferably 0.05% by mass or more, based on 100% by mass of the (meth) acrylic polymer A. Is more preferable, and 0.1% by mass or more is further preferable. Further, the content is preferably 1% by mass or less, more preferably 0.5% by mass or less, and further preferably 0.3% by mass or less. When the content of the silane coupling agent is in the above range, the adhesion to each member in the laminated body can be further improved.
  • the above-mentioned various additives can be added to the pressure-sensitive adhesive composition A, if desired.
  • the polymerization solvent and the diluting solvent are not included in the additives constituting the pressure-sensitive adhesive composition A.
  • the (meth) acrylic polymer A can be produced by polymerizing a mixture of monomers constituting the polymer by a normal radical polymerization method.
  • the polymerization of the (meth) acrylic polymer A is preferably carried out by a solution polymerization method using a polymerization initiator, if desired.
  • the polymerization solvent include ethyl acetate, n-butyl acetate, isobutyl acetate, toluene, acetone, hexane, methyl ethyl ketone and the like, and two or more of them may be used in combination.
  • Examples of the polymerization initiator include azo compounds and organic peroxides, and two or more types may be used in combination.
  • Examples of the azo compound include 2,2'-azobisisobutyronitrile, 2,2'-azobis (2-methylbutyronitrile), 1,1'-azobis (cyclohexane1-carbonitrile), and 2, , 2'-azobis (2,4-dimethylvaleronitrile), 2,2'-azobis (2,4-dimethyl-4-methoxyvaleronitrile), dimethyl 2,2'-azobis (2-methylpropionate) , 4,4'-azobis (4-cyanovaleric acid), 2,2'-azobis (2-hydroxymethylpropionitrile), 2,2'-azobis [2- (2-imidazolin-2-yl) Propane] and the like.
  • organic peroxide examples include benzoyl peroxide, t-butylperbenzoate, cumenehydroperoxide, diisopropylperoxydicarbonate, di-n-propylperoxydicarbonate, and di (2-ethoxyethyl) peroxy.
  • examples thereof include dicarbonate, t-butylperoxyneodecanoate, t-butylperoxyvivarate, (3,5,5-trimethylhexanoyl) peroxide, dipropionyl peroxide, and diacetyl peroxide.
  • the weight average molecular weight of the obtained polymer can be adjusted by adding a chain transfer agent such as 2-mercaptoethanol.
  • a thermal cross-linking agent, a silane coupling agent and, if desired, an additive and a diluting solvent are added to the solution of the (meth) acrylic polymer A and mixed thoroughly.
  • a solvent-diluted pressure-sensitive adhesive composition A (coating solution) can be obtained.
  • the pressure-sensitive adhesive composition A can be produced by a known method, for example, by collectively mixing each component using a mixer or the like. Further, the first pressure-sensitive adhesive composition and the second pressure-sensitive adhesive composition can be prepared from the pressure-sensitive adhesive composition A thus obtained.
  • the component may be dissolved in a diluting solvent by itself in advance. It may be diluted and then mixed with other ingredients.
  • diluting solvent examples include aliphatic hydrocarbons such as hexane, heptane and cyclohexane, aromatic hydrocarbons such as toluene and xylene, halogenated hydrocarbons such as methylene chloride and ethylene chloride, methanol, ethanol, propanol and butanol.
  • Alcohols such as 1-methoxy-2-propanol, ketones such as acetone, methyl ethyl ketone, 2-pentanone, isophorone and cyclohexanone, esters such as ethyl acetate and butyl acetate, and cellosolve solvents such as ethyl cellosolve are used.
  • the concentration and viscosity of the pressure-sensitive adhesive composition A (coating solution) prepared in this manner may be any range as long as it can be coated, and is not particularly limited and can be appropriately selected depending on the situation.
  • the concentration of the pressure-sensitive adhesive composition A can be adjusted to be 10 to 60% by mass in the solution.
  • the addition of a diluting solvent or the like is not a necessary condition, and if the pressure-sensitive adhesive composition A has a coatable viscosity or the like, the diluting solvent may not be added. In this case, the pressure-sensitive adhesive composition A becomes a coating solution using the polymerization solvent of the (meth) acrylic polymer A as it is as a diluting solvent.
  • the pressure-sensitive adhesive layer can be obtained by cross-linking the pressure-sensitive adhesive composition A.
  • Crosslinking of the pressure-sensitive adhesive composition A can be performed by heat treatment.
  • the heat treatment can also serve as a drying treatment for volatilizing the diluting solvent or the like from the coating film of the pressure-sensitive adhesive composition A applied to the desired object.
  • the heating temperature in the heat treatment is preferably 50 to 150 ° C, more preferably 70 to 120 ° C.
  • the heating time in the heat treatment is preferably 10 seconds to 10 minutes, more preferably 50 seconds to 2 minutes.
  • a curing period of about 1 to 2 weeks can be provided at room temperature (for example, 23 ° C., 50% RH) as needed. If this curing period is required, an adhesive layer can be formed after the curing period has elapsed. When the curing period is not required, the pressure-sensitive adhesive layer can be formed after the above-mentioned heat treatment is completed.
  • the (meth) acrylic polymer A is sufficiently cross-linked via the cross-linking agent to form a cross-linked structure, whereby the pressure-sensitive adhesive layers (first pressure-sensitive adhesive layer 102 and second pressure-sensitive adhesive layer 102 and second) are formed.
  • the pressure-sensitive adhesive layer 104) can be obtained.
  • the pressure-sensitive adhesive sheet can include a pressure-sensitive adhesive layer formed from the pressure-sensitive adhesive composition A.
  • the pressure-sensitive adhesive layer can be formed by applying the pressure-sensitive adhesive composition A onto a substrate.
  • an active energy ray-curable pressure-sensitive adhesive composition is used as the pressure-sensitive adhesive composition A
  • the formed pressure-sensitive adhesive layer can be irradiated with active energy rays to obtain a cured product having a desired degree of curing.
  • a thermosetting pressure-sensitive adhesive composition is used as the pressure-sensitive adhesive composition, a cured product having a desired degree of curing can be obtained by subjecting the formed pressure-sensitive adhesive layer to heat treatment (and curing).
  • the base material may be a release film that has undergone a mold release treatment.
  • the pressure-sensitive adhesive sheet can be produced by applying the pressure-sensitive adhesive composition A on a release film to form a pressure-sensitive adhesive layer in the form of a sheet, and then adhering another release film on the pressure-sensitive adhesive layer. it can.
  • a method of applying the coating liquid of the pressure-sensitive adhesive composition A for example, a bar coating method, a knife coating method, a roll coating method, a blade coating method, a die coating method, a gravure coating method and the like can be used.
  • the material and thickness of the front plate 101 are not limited as long as it is a plate-like body capable of transmitting light, and the front plate 101 may be composed of only one layer or may be composed of two or more layers. Examples thereof include a resin plate-like body (for example, a resin plate, a resin sheet, a resin film, etc.), a glass plate-like body (for example, a glass plate, a glass film, etc.), and a touch sensor panel described later.
  • the front plate can constitute the outermost surface of the display device.
  • the thickness of the front plate 101 may be, for example, 10 ⁇ m or more and 1000 ⁇ m or less, preferably 20 ⁇ m or more and 500 ⁇ m or less, and more preferably 30 ⁇ m or more and 300 ⁇ m or less.
  • the thickness of each layer can be measured according to the thickness measuring method described in Examples described later.
  • the resin plate-like body is not limited as long as it can transmit light.
  • the resin constituting the resin plate such as a resin film include triacetyl cellulose, acetyl cellulose butyrate, ethylene-vinyl acetate copolymer, propionyl cellulose, butyryl cellulose, acetyl propionyl cellulose, polyester, and polystyrene.
  • Polyamide polyetherimide, poly (meth) acrylic, polyimide, polyether sulfone, polysulfone, polyethylene, polypropylene, polymethylpentene, polyvinyl chloride, polyvinylidene chloride, polyvinyl alcohol, polyvinyl acetal, polyether ketone, polyether ether ketone , Polyether sulfone, polymethyl methacrylate, polyethylene terephthalate, polybutylene terephthalate, polyethylene naphthalate, polycarbonate, polyamideimide and the like. These polymers can be used alone or in combination of two or more. From the viewpoint of improving strength and transparency, a resin film formed of a polymer such as polyimide, polyamide, or polyamideimide is preferable.
  • the front plate 101 is preferably a film in which a hard coat layer is provided on at least one surface of the base film.
  • a film made of the above resin can be used as the base film.
  • the hard coat layer may be formed on one surface of the base film or may be formed on both surfaces.
  • the hard coat layer is, for example, a cured layer of an ultraviolet curable resin.
  • the ultraviolet curable resin include acrylic resin, silicone resin, polyester resin, urethane resin, amide resin, epoxy resin and the like.
  • the hard coat layer may contain additives to improve strength. Additives are not limited, and include inorganic fine particles, organic fine particles, or mixtures thereof.
  • the front plate 101 is a glass plate
  • tempered glass for a display is preferably used as the glass plate.
  • the thickness of the glass plate may be, for example, 10 ⁇ m or more and 1000 ⁇ m or less, and may be 50 ⁇ m or more and 1000 ⁇ m or less.
  • the front plate 101 not only has a function of protecting the front surface (screen) of the display device (function as a window film), but also has a function as a touch sensor and a blue light cut function. , It may have a viewing angle adjusting function and the like.
  • the first pressure-sensitive adhesive layer 102 is a layer that is interposed between the front plate 101 and the polarizer layer 103 and adheres them, and is, for example, a layer composed of a pressure-sensitive adhesive or an adhesive or some kind of layer. It may be a treated layer.
  • the first pressure-sensitive adhesive layer 102 can be a pressure-sensitive adhesive layer arranged at a position closest to the front plate 101 among the pressure-sensitive adhesive layers constituting the laminated body 100.
  • the "adhesive" as used herein is also referred to as a pressure-sensitive adhesive.
  • the “adhesive” refers to an adhesive other than an adhesive (pressure sensitive adhesive), and is clearly distinguished from the adhesive.
  • the first pressure-sensitive adhesive layer 102 may be one layer or may be composed of two or more layers, but is preferably one layer.
  • the first pressure-sensitive adhesive layer 102 is formed by using the first pressure-sensitive adhesive composition as described above.
  • the first pressure-sensitive adhesive composition can be formed by using the pressure-sensitive adhesive composition A as described above.
  • the first pressure-sensitive adhesive layer 102 uses this first pressure-sensitive adhesive composition to form a first pressure-sensitive adhesive reference layer so that the thickness of the first pressure-sensitive adhesive reference layer and the thickness of the second pressure-sensitive adhesive reference layer are the same.
  • the second pressure-sensitive adhesive reference layer is formed by forming and using the second pressure-sensitive adhesive composition described later, the first pressure-sensitive adhesive reference layer and the second pressure-sensitive adhesive reference layer are represented by the formula ( ⁇ R1> ⁇ R2). Satisfy the relationship of 1).
  • the thickness of the first pressure-sensitive adhesive reference layer and the thickness of the second pressure-sensitive adhesive reference layer can be, for example, 200 ⁇ m.
  • the first pressure-sensitive adhesive composition is not limited to the pressure-sensitive adhesive composition A as long as it satisfies the above formula (1) in relation to the second pressure-sensitive adhesive composition, and can be formed directly from any pressure-sensitive adhesive composition. Alternatively, it can be formed by using a pressure-sensitive adhesive sheet having a pressure-sensitive adhesive layer formed by using any pressure-sensitive adhesive composition.
  • the first pressure-sensitive adhesive composition is preferably formed from the above-mentioned pressure-sensitive adhesive composition A, or is formed by using a pressure-sensitive adhesive sheet formed by applying the above-mentioned pressure-sensitive adhesive composition A on a substrate. Is also preferable.
  • the first pressure-sensitive adhesive layer 102 includes the composition and compounding components of the first pressure-sensitive adhesive composition, the type of the first pressure-sensitive adhesive composition (active energy ray-curable type, heat-curable type, etc.), and the first pressure-sensitive adhesive.
  • the additives that can be blended in the composition the method for producing the first pressure-sensitive adhesive layer, the thickness of the first pressure-sensitive adhesive layer, and the like, the above-mentioned [Adhesive layer (first pressure-sensitive adhesive formed by using the first pressure-sensitive adhesive composition) The layer and the second pressure-sensitive adhesive layer formed by using the second pressure-sensitive adhesive composition)] can be as described in the column.
  • the thickness of the first pressure-sensitive adhesive layer 102 and the second pressure-sensitive adhesive layer 104 preferably has a thickness of 20 ⁇ m or more and 50 ⁇ m or less. Therefore, the thickness of the first pressure-sensitive adhesive layer 102 can be, for example, 3 ⁇ m or more and 100 ⁇ m or less, preferably 5 ⁇ m or more and 50 ⁇ m or less, and may be 20 ⁇ m or more. The thickness of the first pressure-sensitive adhesive layer 102 is most preferably 20 ⁇ m or more and 50 ⁇ m or less.
  • the polarizer layer 103 examples include a stretched film or a stretched layer on which a dichroic dye is adsorbed, a layer obtained by applying and curing a composition containing a dichroic dye and a polymerizable compound, and the like.
  • the dichroic dye specifically, iodine or a dichroic organic dye is used.
  • dichroic organic dyes C.I. I. Included are dichroic direct dyes composed of disuazo compounds such as DIRECT RED 39 and dichroic direct dyes composed of compounds such as trisazo and tetrakisazo.
  • the polarizer layer formed by applying and curing a composition containing a dichroic dye and a polymerizable compound includes a composition containing a dichroic dye having a liquid crystal property or a composition containing a dichroic dye and a polymerizable liquid crystal.
  • a polarizer layer containing a cured product of a polymerizable liquid crystal compound such as a layer obtained by applying and curing an object.
  • a polarizer layer obtained by applying and curing a composition containing a dichroic dye and a polymerizable compound is preferable because there is no limitation in the bending direction as compared with a stretched film or a stretched layer on which a dichroic dye is adsorbed.
  • the polarizer layer 103 can function as a circular polarizing plate, for example, by combining with a retardation layer described later.
  • the polarizer layer which is a stretched film on which a bicolor dye is adsorbed, is usually bicolorized by a step of uniaxially stretching the polyvinyl alcohol-based resin film and dyeing the polyvinyl alcohol-based resin film with the bicolor dye. It can be produced through a step of adsorbing a dye, a step of treating a polyvinyl alcohol-based resin film on which a bicolor dye is adsorbed with an aqueous boric acid solution, and a step of washing with water after the treatment with the aqueous boric acid solution.
  • the thickness of the polarizer layer 103 is, for example, 2 ⁇ m or more and 40 ⁇ m or less.
  • the thickness of the polarizer layer 103 may be 5 ⁇ m or more, 20 ⁇ m or less, further 15 ⁇ m or less, and further 10 ⁇ m or less.
  • the polyvinyl alcohol-based resin is obtained by saponifying the polyvinyl acetate-based resin.
  • the polyvinyl acetate-based resin in addition to polyvinyl acetate, which is a homopolymer of vinyl acetate, a copolymer of vinyl acetate and another monomer copolymerizable therewith is used.
  • examples of other monomers copolymerizable with vinyl acetate include unsaturated carboxylic acids, olefins, vinyl ethers, unsaturated sulfonic acids, and (meth) acrylamides having an ammonium group.
  • the degree of saponification of the polyvinyl alcohol-based resin is usually about 85 mol% or more and 100 mol% or less, preferably 98 mol% or more.
  • the polyvinyl alcohol-based resin may be modified, and for example, polyvinyl formal or polyvinyl acetal modified with aldehydes can be used.
  • the degree of polymerization of the polyvinyl alcohol-based resin is usually 1000 or more and 10000 or less, preferably 1500 or more and 5000 or less.
  • the polarizer layer which is a stretched layer on which a dichroic dye is adsorbed, is usually a step of applying a coating liquid containing the polyvinyl alcohol-based resin on a base film, a step of uniaxially stretching the obtained laminated film, and uniaxial.
  • the base film may be peeled off from the polarizing layer, if necessary.
  • the material and thickness of the base film may be the same as the material and thickness of the thermoplastic resin film described later.
  • the stretched film or the polarizer layer which is a stretched layer, may be incorporated into the laminate in a form in which a thermoplastic resin film is bonded to one side or both sides thereof.
  • This thermoplastic resin film can function as a protective film for the polarizer layer 103 or a retardation film.
  • the thermoplastic resin film is, for example, a polyolefin resin such as a chain polyolefin resin (polypropylene resin, etc.), a cyclic polyolefin resin (norbornen resin, etc.); a cellulose resin such as triacetyl cellulose; polyethylene terephthalate, polyethylene na. It can be a film composed of a polyester resin such as phthalate and polybutylene terephthalate; a polycarbonate resin; a (meth) acrylic resin; or a mixture thereof.
  • the thermoplastic resin film may or may not have a phase difference. From the viewpoint of thinning, the thickness of the thermoplastic resin film is usually 300 ⁇ m or less, preferably 200 ⁇ m or less, more preferably 100 ⁇ m or less, still more preferably 80 ⁇ m or less, still more preferably 60 ⁇ m or less. is there. The thickness of the thermoplastic resin film is usually 5 ⁇ m or more, preferably 20 ⁇ m or more.
  • the thermoplastic resin film can be attached to the polarizer layer 103 by using, for example, an adhesive layer.
  • the polarizer layer formed by applying and curing a composition containing a dichroic dye and a polymerizable compound includes a composition containing a dichroic dye having a liquid crystal property or a dichroic dye and a polymerizable liquid crystal. Examples thereof include a polarizer layer containing a cured product of a polymerizable liquid crystal compound, such as a layer obtained by applying a composition containing the above to a substrate film and curing the composition.
  • the base film may be peeled off from the polarizer layer, if necessary.
  • the material and thickness of the base film may be the same as the material and thickness of the thermoplastic resin film described above.
  • the polarizer layer may include an alignment film. The alignment film may be peeled off.
  • the polarizer layer formed by applying and curing a composition containing a dichroic dye and a polymerizable compound may be incorporated into an optical laminate in the form of a thermoplastic resin film bonded to one or both sides thereof. ..
  • a thermoplastic resin film the same one as the thermoplastic resin film that can be used for the stretched film or the polarizer layer that is the stretched layer can be used.
  • the thermoplastic resin film can be bonded to the polarizer layer using, for example, an adhesive layer.
  • the polarizer layer formed by applying and curing a composition containing a dichroic dye and a polymerizable compound may have an overcoat (OC) layer formed as a protective layer on one side or both sides thereof.
  • OC overcoat
  • examples thereof include photocurable resins and water-soluble polymers.
  • the photocurable resin include (meth) acrylic resin, urethane resin, (meth) acrylic urethane resin, epoxy resin, silicone resin and the like.
  • the water-soluble polymer include poly (meth) acrylamide-based polymers; polyvinyl alcohol, and ethylene-vinyl alcohol copolymers, ethylene-vinyl acetate copolymers, (meth) acrylic acid or its anhydride-vinyl alcohol co-weight.
  • the thickness of the OC layer is preferably 20 ⁇ m or less, more preferably 15 ⁇ m or less, further preferably 10 ⁇ m or less, 5 ⁇ m or less, and 0.05 ⁇ m or more. It may be 0.5 ⁇ m or more.
  • the thickness of the polarizer layer obtained by applying and curing the composition containing the dichroic dye and the polymerizable compound is usually 10 ⁇ m or less, preferably 0.5 ⁇ m or more and 8 ⁇ m or less, and more preferably 1 ⁇ m or more and 5 ⁇ m or less. Is.
  • the second pressure-sensitive adhesive layer 104 is a pressure-sensitive adhesive layer arranged between the polarizer layer 103 and the back plate 105.
  • the second pressure-sensitive adhesive layer can be a pressure-sensitive adhesive layer arranged at a position closest to the back plate 105 among the pressure-sensitive adhesive layers constituting the laminated body 100.
  • the second pressure-sensitive adhesive layer 104 may be one layer or may be composed of two or more layers, but is preferably one layer.
  • the second pressure-sensitive adhesive layer 104 is formed by using the second pressure-sensitive adhesive composition as described above.
  • the second pressure-sensitive adhesive composition can be formed by using the pressure-sensitive adhesive composition A as described above.
  • the second pressure-sensitive adhesive layer 104 uses this second pressure-sensitive adhesive composition to form a second pressure-sensitive adhesive reference layer so that the thickness of the first pressure-sensitive adhesive reference layer and the thickness of the second pressure-sensitive adhesive reference layer are the same.
  • the first pressure-sensitive adhesive reference layer and the second pressure-sensitive adhesive reference layer are represented by the formula ( ⁇ R1> ⁇ R2). Satisfy the relationship of 1).
  • the thickness of the first pressure-sensitive adhesive reference layer and the thickness of the second pressure-sensitive adhesive reference layer can be, for example, 200 ⁇ m.
  • the second pressure-sensitive adhesive composition is not limited to the pressure-sensitive adhesive composition A as long as it satisfies the above formula (1) in relation to the first pressure-sensitive adhesive composition, and can be formed directly from any pressure-sensitive adhesive composition. Alternatively, it can be formed by using a pressure-sensitive adhesive sheet having a pressure-sensitive adhesive layer formed by using any pressure-sensitive adhesive composition.
  • the second pressure-sensitive adhesive composition is preferably formed from the above-mentioned pressure-sensitive adhesive composition A, or is formed by using a pressure-sensitive adhesive sheet formed by applying the above-mentioned pressure-sensitive adhesive composition A on a substrate. Is also preferable.
  • the second pressure-sensitive adhesive layer 104 includes the composition and compounding components of the second pressure-sensitive adhesive composition, the type of the second pressure-sensitive adhesive composition (whether or not it is an active energy ray-curable type or a heat-curable type, etc.). ), Additives that can be blended in the second pressure-sensitive adhesive composition, the method for producing the second pressure-sensitive adhesive layer, the thickness of the second pressure-sensitive adhesive layer, and the like.
  • the first pressure-sensitive adhesive layer and the second pressure-sensitive adhesive layer formed by using the second pressure-sensitive adhesive composition)] can be as described in the column.
  • the thickness of the second pressure-sensitive adhesive layer 104 can be, for example, 3 ⁇ m or more and 100 ⁇ m or less, preferably 5 ⁇ m or more and 50 ⁇ m or less, and may be 20 ⁇ m or more.
  • the thickness of the second pressure-sensitive adhesive layer 104 is most preferably 20 ⁇ m or more and 50 ⁇ m or less.
  • Back plate As the back plate 105, a plate-like body capable of transmitting light, a component used in a normal display device, or the like can be used.
  • the thickness of the back plate 105 may be, for example, 5 ⁇ m or more and 2000 ⁇ m or less, preferably 10 ⁇ m or more and 1000 ⁇ m or less, and more preferably 15 ⁇ m or more and 500 ⁇ m or less.
  • the plate-like body used for the back plate 105 may be composed of only one layer, may be composed of two or more layers, and an example of the plate-like body described in the front plate 101 may be used. it can.
  • Examples of components used in a normal display device used for the back plate 105 include a separator, a touch sensor panel, an organic EL display element, and the like.
  • the stacking order of the components in the display device is, for example, front plate / circular polarizing plate / separator, front plate / circular polarizing plate / organic EL display device, front plate / circular polarizing plate / touch sensor panel / organic EL display element, front. Examples thereof include a face plate / touch sensor panel / circular polarizing plate / organic EL display element.
  • the back plate 105 is preferably a touch sensor panel.
  • touch sensor panel As the touch sensor panel, as long as it is a sensor that can detect the touched position, the detection method is not limited, and the resistance film method, the capacitance coupling method, the optical sensor method, the ultrasonic method, and the electromagnetic induction coupling are used. Examples of touch sensor panels include a method and a surface acoustic wave method. Since the cost is low, a touch sensor panel of a resistive film type or a capacitive coupling type is preferably used.
  • An example of a resistance film type touch sensor panel is a pair of substrates arranged opposite to each other, an insulating spacer sandwiched between the pair of substrates, and a transparent film provided on the inner front surface of each substrate as a resistance film. It is composed of a conductive film and a touch position detection circuit.
  • a touch position detection circuit detects the change in voltage at this time, and the touched position is detected.
  • An example of a capacitively coupled touch sensor panel is composed of a substrate, a transparent electrode for position detection provided on the entire surface of the substrate, and a touch position detection circuit.
  • a capacitance coupling type touch sensor panel when the surface of the front plate is touched, the transparent electrode is grounded through the capacitance of the human body at the touched point.
  • the touch position detection circuit detects the grounding of the transparent electrode, and the touched position is detected.
  • the thickness of the touch sensor panel may be, for example, 5 ⁇ m or more and 2000 ⁇ m or less, and may be 5 ⁇ m or more and 100 ⁇ m or less.
  • the laminated body 100 can have one or more retardation layers between the polarizer layer 103 and the back plate 105.
  • the retardation layer is formed through a first pressure-sensitive adhesive layer 102, a second pressure-sensitive adhesive layer 104, or a layer composed of a pressure-sensitive adhesive or an adhesive other than these layers (hereinafter, also referred to as a bonding layer). (Including other retardation layers.) Can be laminated on top.
  • the retardation layer examples include a positive A plate such as a ⁇ / 4 plate and a ⁇ / 2 plate, a positive C plate, and the like.
  • the retardation layer may be, for example, a retardation film that can be formed from the above-mentioned thermoplastic resin film, or contains a layer obtained by curing a polymerizable liquid crystal compound, that is, a cured product of the polymerizable liquid crystal compound. It may be a layer, but the latter is preferable.
  • the thickness of the retardation film may be the same as the thickness of the above-mentioned thermoplastic resin film.
  • the thickness of the retardation layer obtained by curing the polymerizable liquid crystal compound is, for example, 0.1 ⁇ m or more and 10 ⁇ m or less, preferably 0.5 ⁇ m or more and 8 ⁇ m or less, and more preferably 1 ⁇ m or more and 6 ⁇ m or less.
  • the retardation layer formed by curing the polymerizable liquid crystal compound can be formed by applying a composition containing the polymerizable liquid crystal compound to a base film and curing it.
  • An orientation layer may be formed between the base film and the coating layer.
  • the material and thickness of the base film may be the same as the material and thickness of the thermoplastic resin film described above.
  • the retardation layer formed by curing the polymerizable liquid crystal compound may be incorporated into the laminate 100 in the form of having an alignment layer and / or a base film.
  • the back plate 105 may be a base film to which the above composition is applied.
  • the bonding layer is a layer arranged between the first pressure-sensitive adhesive layer 102 and the second pressure-sensitive adhesive layer 104, and is a layer composed of a pressure-sensitive adhesive or an adhesive.
  • the pressure-sensitive adhesive constituting the bonding layer may be the same pressure-sensitive adhesive as exemplified for the pressure-sensitive adhesive composition constituting the first pressure-sensitive adhesive layer 102 and the second pressure-sensitive adhesive layer 104, or other pressure-sensitive adhesives.
  • it may be a (meth) acrylic pressure-sensitive adhesive, a styrene-based pressure-sensitive adhesive, a silicone-based pressure-sensitive adhesive, a rubber-based pressure-sensitive adhesive, a urethane-based pressure-sensitive adhesive, a polyester-based pressure-sensitive adhesive, an epoxy-based copolymer pressure-sensitive adhesive, or the like.
  • the adhesive constituting the bonded layer for example, one or two or more of water-based adhesives, active energy ray-curable adhesives, adhesives and the like can be combined to form the adhesive.
  • the water-based adhesive include a polyvinyl alcohol-based resin aqueous solution, a water-based two-component urethane-based emulsion adhesive, and the like.
  • the active energy ray-curable adhesive is an adhesive that cures by irradiating with active energy rays such as ultraviolet rays, and includes, for example, a polymerizable compound and a photopolymerizable initiator, a photoreactive resin, and the like. Examples thereof include those containing a binder resin and a photoreactive cross-linking agent.
  • Examples of the polymerizable compound include photopolymerizable monomers such as a photocurable epoxy monomer, a photocurable acrylic monomer, and a photocurable urethane monomer, and oligomers derived from these monomers.
  • Examples of the photopolymerization initiator include substances that generate active species such as neutral radicals, anionic radicals, and cationic radicals by irradiating them with active energy rays such as ultraviolet rays.
  • the thickness of the bonded layer may be, for example, 1 ⁇ m or more, preferably 1 ⁇ m or more and 25 ⁇ m or less, more preferably 2 ⁇ m or more and 15 ⁇ m or less, and further preferably 2.5 ⁇ m or more and 5 ⁇ m or less.
  • the laminate 200 includes a front plate 101, a first pressure-sensitive adhesive layer 102, a polarizer layer 103, a second pressure-sensitive adhesive layer 104, and a back surface plate 105.
  • the bonded layer 108, the first retardation layer 106, the bonding layer 109, and the second retardation layer 107 can be further provided.
  • the laminates 100 and 200 can be manufactured by a method including a step of laminating the layers constituting the laminates 100 and 200 via an adhesive layer or an adhesive layer.
  • a surface activation treatment such as corona treatment for the purpose of improving adhesion. preferable.
  • the polarizer layer 103 can be formed directly on the thermoplastic resin film or the base film, and the thermoplastic resin film or the base film may be incorporated into the laminates 100 and 200, or It does not have to be separated from the polarizer layer 103 to become a component of the laminate.
  • the display device includes the above-mentioned laminates 100 and 200.
  • the display device is not particularly limited, and examples thereof include an image display device such as an organic EL display device, an inorganic EL display device, a liquid crystal display device, and an electroluminescent display device.
  • the display device may have a touch panel function. Since the laminates 100 and 200 have improved durability by suppressing the generation of air bubbles in the pressure-sensitive adhesive layer, they are suitable for a flexible display device capable of bending or bending.
  • the laminated bodies 100 and 200 are arranged on the visible side of the display element of the display device with the front plate facing the outside (the side opposite to the display element side, that is, the visual recognition side). It is preferable that the display device can be bent with the front plate 101 side of the laminated bodies 100 and 200 facing outward.
  • the display device can be used as a mobile device such as a smartphone or tablet, a television, a digital photo frame, an electronic signboard, a measuring instrument, an instrument, an office device, a medical device, a computer device, or the like.
  • the weight average molecular weight (Mw) of the (meth) acrylic polymer A was determined by the following size exclusion chromatography (SEC) using tetrahydrofuran as the mobile phase as the polystyrene-equivalent number average molecular weight (Mn).
  • the (meth) acrylic polymer A to be measured was dissolved in tetrahydrofuran at a concentration of about 0.05% by mass, and 10 ⁇ L was injected into SEC. The mobile phase was flowed at a flow rate of 1.0 mL / min.
  • PLgel MIXED-B manufactured by Polymer Laboratories
  • a UV-VIS detector (trade name: Agilent GPC) was used as the detector.
  • ⁇ Layer thickness> The measurement was performed using a contact type film thickness measuring device (“MS-5C” manufactured by Nikon Corporation). However, the polarizer layer and the alignment film were measured using a laser microscope (“OLS3000” manufactured by Olympus Corporation).
  • the strain repeated addition test was performed by using a viscoelasticity measuring device (MCR-301, Antonio Par).
  • the specific test method is as follows. That is, an adhesive having a thickness of 200 ⁇ m is obtained by cutting an adhesive sheet (adhesive sheet A11, adhesive sheet A12, etc.) on which an adhesive layer described later is formed into a width of 20 mm ⁇ a length of 20 mm, peeling off a release film, and laminating eight sheets.
  • a reference layer (a first pressure-sensitive adhesive reference layer and a second pressure-sensitive adhesive reference layer) was formed. Next, this pressure-sensitive adhesive reference layer was bonded to a glass plate.
  • the shear creep value (unit: "%") at 25 ° C. was determined using the following methods. That is, the shear creep value at 25 ° C. was determined by measuring using the above-mentioned viscoelasticity measuring device (MCR-301, Antonio Par). Specifically, the temperature of the pressure-sensitive adhesive reference layer on the glass plate before the strain repeated addition test or after the strain repeated addition test is adhered to the measuring chip in the apparatus. The shear creep value at that time was determined by allowing 1200 seconds to elapse under the conditions of 25 ° C., Normal Force 1N, and Torque 1200 ⁇ Nm.
  • each value obtained as the shear creep value before and after executing the strain repeated addition test was divided by the thickness (200 ⁇ m) of the first pressure-sensitive adhesive reference layer or the second pressure-sensitive adhesive reference layer.
  • the second shear creep rate (R1B) which is the shear creep value per 1 ⁇ m of the thickness of the first pressure-sensitive adhesive reference layer before the addition test is performed, and the thickness of 1 ⁇ m with respect to the second pressure-sensitive adhesive reference layer after the strain repeated addition test is performed.
  • the third shear creep rate (R2A), which is the shear creep value per unit, and the fourth first shear creep rate (R2A), which is the shear creep value per 1 ⁇ m in thickness with respect to the second pressure-sensitive adhesive reference layer before performing the strain iterative addition test. R2B) was calculated. Subsequently, the second shear creep rate was subtracted from the first shear creep rate, and the fourth shear creep rate was subtracted from the third shear creep rate, so that the subtracted values were obtained as ⁇ R1 and ⁇ R2, respectively.
  • the gel fraction of the pressure-sensitive adhesive layer (the pressure-sensitive adhesive layer A11 and the pressure-sensitive adhesive layer A12) was measured according to the following (I) to (V).
  • a pressure-sensitive adhesive layer having an area of about 8 cm ⁇ about 8 cm and a metal mesh (whose mass is Wm) made of SUS304 having an area of about 10 cm ⁇ about 10 cm are bonded together.
  • (meth) acrylic polymer A This is referred to as (meth) acrylic polymer A.
  • the structural unit derived from 2-hydroxyethyl acrylate, which is a hydroxyl group-containing unsaturated monomer in the (meth) acrylic polymer A, is 1% by mass, and is derived from acrylic acid, which is a carboxyl group-containing unsaturated monomer.
  • the structural unit to be used is 0.4% by mass.
  • Adhesive Composition A11 100 parts by mass (solid content conversion value; the same applies hereinafter) of the (meth) acrylic polymer A obtained in the above step and polyisocyanate as a thermal cross-linking agent B (manufactured by Toso Co., Ltd., Product name "Coronate L”) and 3-glycidoxypropyltrimethoxysilane (manufactured by Shinetsu Chemical Industry Co., Ltd., product name "KBM403”) as a silane coupling agent C are mixed, stirred well and diluted with methyl ethyl ketone. A coating solution of the pressure-sensitive adhesive composition A11 was obtained.
  • Table 1 shows each formulation (solid content conversion value) of the pressure-sensitive adhesive composition A11 when the (meth) acrylic polymer is 100 parts by mass (solid content conversion value).
  • the abbreviation "BA” in Table 1 represents n-butyl acrylate, "2EHA” represents 2-ethylhexyl acrylate, and "AA” represents acrylic acid.
  • the Tg (° C.) of these BA, 2EHA and AA was determined by differential thermal analysis (DTA).
  • the pressure-sensitive adhesive layer of the pressure-sensitive adhesive sheet A11 is also referred to as the pressure-sensitive adhesive layer A11.
  • Adhesive Composition A12 With respect to 100 parts by mass of the (meth) acrylic polymer A, the amount of Coronate L, which is a heat-crosslinking agent, is as shown in Table 1, but the pressure-sensitive adhesive composition A11. A coating solution of the pressure-sensitive adhesive composition A12 was obtained by using the same preparation method.
  • the pressure-sensitive adhesive sheet A12 was produced by using the coating solution of the pressure-sensitive adhesive composition A12 in the same manner as in the production process of the pressure-sensitive adhesive sheet A11.
  • the pressure-sensitive adhesive layer of the pressure-sensitive adhesive sheet A12 is also referred to as the pressure-sensitive adhesive layer A12.
  • Table 1 shows each formulation (solid content conversion value) of the pressure-sensitive adhesive composition A12 when the (meth) acrylic polymer is 100 parts by mass (solid content conversion value). Table 1 also shows the gel fraction values of the pressure-sensitive adhesive composition A11 and the pressure-sensitive adhesive composition A12 obtained by the above method.
  • OCA8146-02 and CEF3004 were prepared as commercially available adhesive sheets.
  • Adhesive Composition B11 The contents of the above (meth) acrylic polymer B1, the active energy ray-polymerizable compound, and the photopolymerization initiator are mixed so as to be in the ratio shown in Table 3. The pressure-sensitive adhesive composition B11 was produced.
  • Adhesive Sheet B11 The adhesive composition B11 was applied onto a release film that had been subjected to a silicon mold release treatment so as to have a thickness of 25 ⁇ m. After further laminating a release film on the coating film, an adhesive sheet B11 was prepared by irradiating with ultraviolet rays (integrated light amount 400 mJ / cm 2 , illuminance 1.8 mW / cm 2 , UVV standard).
  • the pressure-sensitive adhesive layer of the pressure-sensitive adhesive sheet B11 is also referred to as a pressure-sensitive adhesive layer B11.
  • Adhesive Composition B21 The contents of the (meth) acrylic polymer B2, the active energy ray-polymerizable compound, and the photopolymerization initiator are mixed so as to be in the ratios shown in Table 3. The pressure-sensitive adhesive composition B21 was produced.
  • Adhesive Sheet B21 The adhesive composition B21 was applied onto a release film that had been subjected to a silicon mold release treatment so as to have a thickness of 25 ⁇ m. After further laminating a release film on the coating film, an adhesive sheet B21 was prepared by irradiating with ultraviolet rays (integrated light amount 400 mJ / cm 2 , illuminance 1.8 mW / cm 2 , UVV standard).
  • the pressure-sensitive adhesive layer of the pressure-sensitive adhesive sheet B21 is also referred to as a pressure-sensitive adhesive layer B21.
  • LA lauryl acrylate
  • 2-EHA 2-ethylhexyl acrylate
  • 2-HEA 2-hydroxyethyl acrylate
  • 2-PHA 2-propyl heptyl acrylate
  • C22A represents behenyl acrylate
  • ODA octyl decyl acrylate
  • IBOA isobornyl acrylate
  • a pressure-sensitive adhesive reference layer having a thickness of 200 ⁇ m was prepared for each of the above-mentioned pressure-sensitive adhesive sheets according to the above-mentioned method, and the strain repeat-addition test was performed before and after the strain-repeated addition test was performed on each pressure-sensitive adhesive reference layer. Later, the shear creep value (%) and the difference in shear creep rate (% / ⁇ m) were determined. The results are shown in Table 4. Table 4 also shows the numerical values of the shear creep rate (% / ⁇ m) before performing the strain repeated addition test in each pressure-sensitive adhesive reference layer.
  • TAC film with a thickness of 25 ⁇ m 2 Composition for forming an alignment film ⁇ Polymer 1> Polymer 1 having a photoreactive group consisting of the following structural units was prepared.
  • composition (D-1) A solution in which polymer 1 was dissolved in cyclopentanone at a concentration of 5% by mass was prepared as a composition for forming an alignment film [hereinafter, also referred to as composition (D-1)].
  • composition for forming a polarizer layer As the polymerizable liquid crystal compound, the polymerizable liquid crystal compound represented by the formula (1-1) [hereinafter, also referred to as compound (1-1)] and the polymerizable liquid crystal compound represented by the formula (1-2) [hereinafter, Compound (1-2)] was prepared.
  • ⁇ Dichroic pigment> As the dichroic dye, the azo dye described in Examples of Japanese Patent Application Laid-Open No. 2013-101328 represented by the following formulas (2-1a), (2-1b) and (2-3a) was prepared.
  • composition (A-1) has 75 parts by mass of compound (1-1), 25 parts by mass of compound (1-2), and the above formula as a bicolor dye.
  • BYK-361N polyacrylate compound manufactured by BYK-Chemie
  • composition for forming a protective layer [hereinafter, also referred to as composition (E-1)] is water: 100 parts by mass, polyvinyl alcohol resin powder (Co., Ltd.). ) Made by Kuraray, average degree of polymerization 18000, trade name: KL-318): 3 parts by mass, polyamide epoxy resin (crosslinking agent, manufactured by Sumika Chemtex Co., Ltd., trade name: SR650 (30)): 1.5 parts by mass Was prepared by mixing.
  • the composition for forming an alignment film was coated on the TAC film side as follows. That is, first, the TAC film side was subjected to the corona treatment once. The conditions for corona treatment were an output of 0.3 kW and a processing speed of 3 m / min. Then, the composition (D-1) obtained as described above was applied onto the TAC by the bar coating method, and dried by heating in a drying oven at 80 ° C. for 1 minute. The obtained dry film was subjected to polarized UV irradiation treatment to form a first alignment film (AL1).
  • A1 first alignment film
  • the light emitted from the UV irradiation device (SPOT CURE SP-7; manufactured by Ushio, Inc.) is transmitted through a wire grid (UIS-27132 ##, manufactured by Ushio, Inc.) to have a wavelength of 365 nm.
  • the test was performed under the condition that the integrated light amount measured in 1 was 100 mJ / cm 2 .
  • the thickness of the first alignment film (AL1) was 100 nm.
  • composition for forming a polarizer layer was coated on the alignment film side as follows. That is, first, the composition (A-1) was applied onto the first alignment film (AL1) by the bar coating method, heated and dried in a drying oven at 120 ° C. for 1 minute, and then cooled to room temperature.
  • a polarizing layer (pol) was formed by irradiating the dry film with ultraviolet rays at an integrated light amount of 1200 mJ / cm 2 (365 nm standard) using the above UV irradiation device. The thickness of the obtained polarizer layer (pol) was measured with a laser microscope (OLS3000 manufactured by Olympus Corporation) and found to be 1.8 ⁇ m. In this way, a laminate composed of "TAC / AL1 / pol" was obtained.
  • composition for forming a protective layer was coated on the polarizer layer side as follows. That is, the composition (E-1) is applied onto the polarizer layer (pol) by a bar coating method, coated so that the thickness after drying is 1.0 ⁇ m, and the temperature is 80 ° C. for 3 minutes. It was dry. In this way, a laminate composed of "TAC film / cPL (AL1 + pol + protective layer)" was obtained.
  • composition (D-1) Composition (D-1)).
  • composition for forming a retardation layer The composition (B-1) was obtained by mixing each of the following components and stirring the obtained mixture at 80 ° C. for 1 hour.
  • Polymerization initiator (Irgacure369, 2-dimethylamino-2-benzyl-1- (4-morpholinophenyl) butane-1-one, manufactured by BASF Japan Ltd.): 6 parts by mass leveling agent (BYK-361N, polyacrylate compound, BYK) -Chemie): 0.1 parts by mass Solvent (cyclopentanone): 400 parts by mass.
  • the composition for forming an alignment film was coated on the PET film as follows. That is, a polyethylene terephthalate film (PET) having a thickness of 100 ⁇ m was prepared as a base material, the composition (D-1) was applied onto the film by the bar coating method, and the film was heated and dried in a drying oven at 80 ° C. for 1 minute. The obtained dry film was subjected to polarized UV irradiation treatment to form a second alignment film (AL2). The polarized UV treatment was carried out under the condition that the integrated light amount measured at a wavelength of 365 nm was 100 mJ / cm 2 using the above UV irradiation device. The polarization direction of the polarized UV was set to 45 ° with respect to the absorption axis of the polarizer layer. In this way, a laminate composed of "base material (PET) / second alignment film (AL2)" was obtained.
  • PET polyethylene terephthalate film
  • AL2 polarized UV irradiation treatment
  • composition for forming a retardation layer was coated on the alignment film side of the PET film as follows. That is, the composition (B-1) is applied on the second alignment film (AL2) of the laminate composed of the above “base material (PET) / second alignment film (AL2)" by the bar coating method, and the temperature is 120 ° C. After heating and drying in a drying oven for 1 minute, the mixture was cooled to room temperature. A retardation layer was formed by irradiating the obtained dry film with ultraviolet rays having an integrated light intensity of 1000 mJ / cm 2 (365 nm standard) using the above UV irradiation device.
  • the thickness of the obtained retardation layer was measured with a laser microscope (OLS3000 manufactured by Olympus Corporation) and found to be 2.0 ⁇ m.
  • the retardation layer was a ⁇ / 4 plate (QWP) showing a retardation value of ⁇ / 4 in the in-plane direction. In this way, a laminate composed of "base material (PET) / retardation portion (AL2 + QWP)" was obtained.
  • Acrylic resin 100 parts by mass Cross-linking agent (“Coronate L” manufactured by Tosoh Corporation): 1.0 parts by mass Silane coupling agent (“X-12-981” manufactured by Shin-Etsu Chemical Co., Ltd.): 0.5 parts by mass.
  • the above pressure-sensitive adhesive composition was prepared by adding ethyl acetate so that the total solid content concentration was 10% by mass.
  • Laminates were manufactured by the procedure shown in FIGS. 3A to 3E.
  • the above-mentioned polarizer layer 410 [TAC film 301 / cPL ((AL1 + pol) 302 / OC layer 303)] and the above-mentioned common adhesive sheet 420 (light separator 304 / common adhesive layer). 305 / heavy separator 306) was prepared.
  • corona treatment output 0.3 kW, processing speed 3 m / min
  • the first laminated body precursor 430 shown in FIG. 3 (b) was obtained. Further, as shown in FIG. 3B, the above-mentioned retardation layer 440 [base material (PET) 308 / retardation section (AL2 + QWP) 307] was prepared.
  • the surface from which the retardation portion 307 side of the retardation layer 440 and the heavy separator 306 of the first laminated body precursor 430 were peeled off was subjected to corona treatment (output 0.3 kW, processing speed 3 m / min), and then.
  • corona treatment output 0.3 kW, processing speed 3 m / min
  • the second laminated body precursor 450 shown in FIG. 3C was obtained.
  • the pressure-sensitive adhesive sheet A11 was prepared as the pressure-sensitive adhesive sheet 460 (first release film 309 / adhesive layer 310 / second release film 311).
  • the pressure-sensitive adhesive layer 310 of the pressure-sensitive adhesive sheet 460 corresponds to the second pressure-sensitive adhesive layer.
  • Corona treatment (output 0.3 kW, processing speed 3 m / min) was applied to the surface from which the base material (PET) 308 of the second laminate precursor 450 was peeled off and the surface from which the first release film 309 of the adhesive sheet 460 was peeled off.
  • the third laminated precursor precursor 470 shown in FIG. 3D was obtained by laminating.
  • the adhesive sheet A12 was prepared as the adhesive sheet 490 (first release film 314 / adhesive layer 315 / second release film 316), and the surface from which the first release film 314 was peeled and the above-mentioned front plate 480 (polyimide) were prepared.
  • 3D is formed by applying corona treatment (output 0.3 kW, processing speed 3 m / min) to the polyimide film 313 side of the film 313 / hard coat layer 312) and then laminating them. A precursor 500 was obtained.
  • the pressure-sensitive adhesive layer 315 of the pressure-sensitive adhesive sheet 490 corresponds to the first pressure-sensitive adhesive layer.
  • the surface from which the second release film 316 of the fourth laminated body precursor 500 was peeled off and the TAC301 side of the third laminated body precursor 470 were subjected to corona treatment (output 0.3 kW, processing speed 3 m / min).
  • the sixth laminated body precursor 300 shown in FIG. 3 (e) was obtained by laminating.
  • the second release film 311 was peeled off in the sixth laminated body precursor 300, and the peeled surface and one surface of the PET film having a thickness of 100 ⁇ m prepared as the back plate were subjected to corona treatment (output 0.3 kW,
  • the laminate of Example 1 was obtained by laminating after applying a treatment speed of 3 m / min).
  • the laminate of Example 1 has a thickness of 240 ⁇ m and a shape of 190 mm in length ⁇ 150 mm in width.
  • Examples 2 to 5, Comparative Examples 1 to 2 By applying the same manufacturing method as the laminate of Example 1 except that the pressure-sensitive adhesive sheet having the pressure-sensitive adhesive layer shown in Table 5 was used instead of the pressure-sensitive adhesive sheets A11 and A12 used in Example 1, Examples Laminates of 2 to 5 and Comparative Examples 1 and 2 were produced.
  • Table 5 lists the types of pressure-sensitive adhesive compositions used to form the first pressure-sensitive adhesive layer and the second pressure-sensitive adhesive layer with respect to the laminates of Examples 1 to 5 and Comparative Examples 1 and 2. .. Examples 1 to 5 satisfy the relationship of ⁇ R1> ⁇ R2, and Comparative Examples 1 and 2 have a relationship of ⁇ R1 ⁇ ⁇ R2.
  • ⁇ Bending durability test (mandrel test)> A test piece having a length of 100 mm and a width of 10 mm was cut out from the laminated body of each Example and each Comparative Example using a super cutter.
  • a bending resistance tester (cylindrical mandrel method) manufactured by TP Giken Co., Ltd. was used, and the test piece was placed on a cylindrical mandrel (cylindrical mandrel method) so that the back plate of the test piece (laminate) was on the inside.
  • a bending durability test (mandrel test) was performed in which the test piece was bent along the length direction at a temperature of 25 ° C. by wrapping it around the mandrel).
  • the minimum diameter of the mandrel that does not generate air bubbles in the pressure-sensitive adhesive layer of the test piece (laminated body) was determined, and ranked based on the following criteria.
  • the bending durability test it can be evaluated that the smaller the value of this minimum diameter, the better the bending durability of the pressure-sensitive adhesive layer.
  • D Bubbles were generated in the pressure-sensitive adhesive layer when wound around a mandrel exceeding ⁇ 20 mm.
  • ⁇ Surface hardness test> A pencil hardness tester (PHT, manufactured by SUKBO SCIENCE Co., Ltd.) was used to apply a load of 100 g to the surface of the back plate in the laminate of each example and each comparative example at a temperature of 25 ° C. A concave mark was formed on the surface with a pencil (manufactured by Mitsubishi Pencil Co., Ltd., core hardness is 6B).
  • the surface hardness of the laminates of each Example and each Comparative Example was evaluated by determining the time until the recess marks disappeared and ranking them based on the following criteria. In this surface hardness test, it can be evaluated that the shorter the time until the recess marks disappear, the better the surface hardness.
  • C Recess marks disappeared in 60 minutes or more and less than 90 minutes
  • D Recess marks disappeared even after 90 minutes passed Did not disappear.
  • Examples 1 to 5 satisfy the relationship of ⁇ R1> ⁇ R2 and are superior in evaluation of bending durability and surface hardness to Comparative Examples 1 and 2 having a relationship of ⁇ R1 ⁇ ⁇ R2.

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  • Physics & Mathematics (AREA)
  • Engineering & Computer Science (AREA)
  • General Physics & Mathematics (AREA)
  • Optics & Photonics (AREA)
  • Nonlinear Science (AREA)
  • Theoretical Computer Science (AREA)
  • General Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Mathematical Physics (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Mechanical Engineering (AREA)
  • Human Computer Interaction (AREA)
  • Organic Chemistry (AREA)
  • Laminated Bodies (AREA)
  • Liquid Crystal (AREA)
  • Adhesive Tapes (AREA)
  • Adhesives Or Adhesive Processes (AREA)
  • Polarising Elements (AREA)

Abstract

Le but de la présente invention est de fournir un corps multicouche qui présente une durabilité améliorée par suppression de la génération de bulles d'air dans une couche adhésive. La présente invention concerne un corps multicouche qui comprend séquentiellement une plaque avant, une première couche adhésive qui est formée à l'aide d'une première composition adhésive, une couche de polariseur, une seconde couche adhésive qui est formée à l'aide d'une seconde composition adhésive, et une plaque arrière dans cet ordre, et qui est configurée de telle sorte que si une première couche de base adhésive est formée à l'aide de la première composition adhésive et qu'une seconde couche de base adhésive est formée à l'aide de la seconde composition adhésive de telle sorte que l'épaisseur de la première couche de base adhésive est égale à l'épaisseur de la seconde couche de base adhésive, la première couche de base adhésive et la seconde couche de base adhésive satisfont l'expression relationnelle ∆R1 > ∆R2.
PCT/JP2020/006272 2019-03-18 2020-02-18 Corps multicouche et dispositif d'affichage le comprenant WO2020189146A1 (fr)

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CN113614589B (zh) 2023-09-22
JP2020154309A (ja) 2020-09-24

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