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WO2018159377A1 - Dispositif d'affichage d'image et procédé de fabrication dudit dispositif d'affichage d'image - Google Patents

Dispositif d'affichage d'image et procédé de fabrication dudit dispositif d'affichage d'image Download PDF

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Publication number
WO2018159377A1
WO2018159377A1 PCT/JP2018/005906 JP2018005906W WO2018159377A1 WO 2018159377 A1 WO2018159377 A1 WO 2018159377A1 JP 2018005906 W JP2018005906 W JP 2018005906W WO 2018159377 A1 WO2018159377 A1 WO 2018159377A1
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WO
WIPO (PCT)
Prior art keywords
polarizing plate
display device
image display
liquid crystal
stretching
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/JP2018/005906
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English (en)
Japanese (ja)
Inventor
後藤　周作
岸　敦史
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Nitto Denko Corp
Original Assignee
Nitto Denko Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Nitto Denko Corp filed Critical Nitto Denko Corp
Priority to KR1020197021901A priority Critical patent/KR102580443B1/ko
Priority to CN201880013947.2A priority patent/CN110326036A/zh
Priority to JP2019502895A priority patent/JPWO2018159377A1/ja
Publication of WO2018159377A1 publication Critical patent/WO2018159377A1/fr
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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Classifications

    • 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
    • H10K59/87—Passivation; Containers; Encapsulations
    • H10K59/871—Self-supporting sealing arrangements
    • H10K59/8722—Peripheral sealing arrangements, e.g. adhesives, sealants
    • 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
    • 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
    • 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
    • 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
    • G09F9/30—Indicating arrangements for variable information in which the information is built-up on a support by selection or combination of individual elements in which the desired character or characters are formed by combining individual elements
    • 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
    • H05B33/10—Apparatus or processes specially adapted to the manufacture of electroluminescent light sources
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K50/00—Organic light-emitting devices
    • H10K50/10—OLEDs or polymer light-emitting diodes [PLED]
    • 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
    • H10K59/8793—Arrangements for polarized light emission

Definitions

  • the present invention relates to an image display device and a method for manufacturing the image display device.
  • Image display devices eg, liquid crystal display devices, organic EL display devices, quantum dot display devices
  • a polarizing plate disposed on at least one side of the display cell due to the image forming method.
  • the polarizing plate has a durability problem that the optical properties of the polarizing film that substantially dominate the optical properties of the polarizing plate are deteriorated in a humidified environment. More specifically, the polarizing film loses the polarization performance at the end in a humidified environment, and as a result, a phenomenon of so-called color loss may occur in the image display device.
  • the present invention has been made to solve the above-mentioned problems, and a main object of the present invention is to provide an image display device capable of maintaining excellent optical characteristics even in a humidified environment and preventing color loss and such an image display.
  • the object is to provide a simple manufacturing method of the apparatus.
  • the image display device of the present invention includes a display cell, a polarizing plate disposed on at least one side of the display cell, and a sealing portion that covers a peripheral end surface of the polarizing plate.
  • This polarizing plate contains the polarizing film comprised with the polyvinyl alcohol-type resin film containing iodine, and the water vapor transmission rate of this sealing part is 300 g / m ⁇ 2 > / 24hr or less.
  • the sealing portion covers the entire surface of the polarizing plate opposite to the display cell and the entire peripheral end surface.
  • the sealing portion has a thickness of 10 ⁇ m to 100 ⁇ m.
  • the said sealing part is comprised with the adhesive composition.
  • the sealing part is made of a rubber-based adhesive.
  • the image display device further includes a cover glass disposed on the opposite side of the polarizing plate to the display cell.
  • the image display device has an amount of color loss of 100 ⁇ m or less after being held at 85 ° C. and 85% RH for 120 hours.
  • a method for manufacturing an image display device includes disposing a polarizing plate on one side of the display cell, and forming a sealing portion so as to cover a peripheral end face of the polarizing plate.
  • This polarizing plate contains the polarizing film comprised with the polyvinyl alcohol-type resin film containing iodine, and the water vapor transmission rate of this sealing part is 300 g / m ⁇ 2 > / 24hr or less.
  • the manufacturing method includes forming a sealing portion so as to cover the entire surface of the polarizing plate opposite to the display cell and the entire peripheral end surface.
  • the said manufacturing method includes forming a sealing part by arrange
  • the size of the sheet is larger than the polarizing plate, and the manufacturing method arranges the sheet so as to cover the entire surface of the polarizing plate opposite to the display cell and the entire peripheral end surface. Forming a sealing portion.
  • the manufacturing method further includes disposing a cover glass on the side of the polarizing plate opposite to the display cell.
  • the manufacturing method includes an adhesive composition and covers the entire surface opposite to the display cell and the entire peripheral end surface using a sheet having a size larger than that of the polarizing plate. Forming the sealing portion by disposing the sheet. According to such an embodiment, an excellent optical characteristic can be maintained even in a humidified environment, and an image display device in which color loss is prevented can be manufactured very simply.
  • FIG. 1 is a schematic partial cross-sectional view of an image display device according to an embodiment of the present invention. It is a schematic diagram for demonstrating calculation of the amount of color loss. It is the schematic for demonstrating an example of the manufacturing method of the image display apparatus of this invention.
  • 6 is an image showing a color loss amount after a humidification test of a liquid crystal display device alternative corresponding to Example 1.
  • FIG. It is an image which shows the color loss amount after the humidification test of the liquid crystal display device alternative corresponding to the comparative example 1.
  • the present invention can be applied to an image display device having a polarizing plate on at least one side of a display cell.
  • an image display device include a liquid crystal display device, an organic electroluminescence (EL) display device, and a quantum dot display device.
  • EL organic electroluminescence
  • quantum dot display device a quantum dot display device.
  • an embodiment in which the present invention is applied to a viewing side portion of a liquid crystal display device will be described as an example. It will be apparent to those skilled in the art that the present invention can be applied to the back side portion of the liquid crystal display device, the organic EL display device, and the quantum dot display device as well as the viewing side portion of the liquid crystal display device.
  • FIG. 1 is a schematic partial cross-sectional view of an image display device according to an embodiment of the present invention, and more specifically, a schematic cross-sectional view of a viewing side portion of a liquid crystal display device.
  • the liquid crystal display device 100 of FIG. 1 includes a liquid crystal cell 10, a polarizing plate 20 disposed on the viewing side of the liquid crystal cell 10, and a sealing unit 30 that covers a peripheral end surface of the polarizing plate 20.
  • the polarizing plate 20 includes a polarizing film 21.
  • the protective film 22 is disposed on one side of the polarizing film 21 (the side opposite to the liquid crystal cell). However, the protective film may be disposed on the liquid crystal cell side of the polarizing film depending on the purpose or the like. It may be arranged.
  • the pressure-sensitive adhesive layer 50 is provided as the outermost layer on the liquid crystal cell 10 side of the polarizing plate 20, and the polarizing plate 10 is bonded to the liquid crystal cell 10 through the pressure-sensitive adhesive layer 50.
  • the liquid crystal display device 100 typically further includes a cover glass 40 disposed on the viewing side (the side opposite to the liquid crystal cell) of the polarizing plate 20. When a cover glass is provided, the protective film 22 may be omitted.
  • the liquid crystal cell and the back side portion of the liquid crystal display device may each employ a well-known configuration in the industry, and thus will not be described in detail.
  • the polarizing film 21 is composed of a polyvinyl alcohol resin (hereinafter referred to as “PVA resin”) film containing iodine.
  • PVA resin polyvinyl alcohol resin
  • the thickness of the polarizing film is typically 8 ⁇ m or less.
  • the polarizing film contains iodine and the thickness thereof is very thin, the iodine density in the polarizing film increases, and the stability of iodine due to humidification tends to decrease, so a sealing portion is provided. The effect becomes more remarkable.
  • the moisture permeability of the sealing portion is not more than 300g / m 2 / 24hr.
  • the sealing part 30 only needs to cover the peripheral end surfaces of the polarizing plate 20 (that is, the polarizing film 21 and the protective film 22), and the peripheral end surfaces of the pressure-sensitive adhesive layer 50 may cover the whole, and partially. It may or may not be covered.
  • the sealing portion 30 covers the peripheral end surfaces of the polarizing plate 20 and the pressure-sensitive adhesive layer 50.
  • the sealing part 30 may cover only the peripheral end surface of the polarizing plate 20, or may cover a portion other than the peripheral end surface together with the peripheral end surface.
  • the sealing unit 30 covers the entire surface of the peripheral end surface of the polarizing plate and the entire surface of the polarizing plate opposite to the liquid crystal cell 10.
  • the sealing part 30 should just cover the surrounding end surface of the polarizing plate 20, and the said surrounding end surface is sealed, and does not need to be closely_contact
  • the amount of color loss after being held at 85 ° C. and 85% RH for 120 hours is preferably 100 ⁇ m or less, more preferably 50 ⁇ m or less. More preferably, it is 30 ⁇ m or less, and particularly preferably 25 ⁇ m or less.
  • the lower limit of the amount of color loss is preferably zero, and in one embodiment is 5 ⁇ m.
  • the amount of color loss can be calculated as follows: From a polarizing plate (or polarizing film), a test piece of a predetermined size is cut out with a direction perpendicular to the stretching direction and two sides facing each other in the stretching direction.
  • the stretching direction typically corresponds to the absorption axis direction of the polarizing film.
  • stretching direction can respond
  • MD direction elongate direction
  • the test piece is bonded to a glass plate with an adhesive to obtain a substitute for a liquid crystal display device.
  • This liquid crystal display device substitute is left to humidify in an oven at 85 ° C. and 85% RH for 120 hours.
  • the humidified test piece is placed in the state of a standard polarizing plate and crossed Nicols, the color loss state at the end of the humidified test piece is examined with a microscope.
  • the magnitude of color loss (color loss amount: ⁇ m) from the end of the test piece (polarizing plate or polarizing film) is measured.
  • the larger one of the color loss amount a from the end portion in the stretching direction and the color loss amount b from the end portion in the direction orthogonal to the stretching direction is defined as the color loss amount.
  • the color loss region has extremely low polarization characteristics and does not substantially function as a polarizing plate. Therefore, the smaller the color loss amount, the better.
  • the configuration of the polarizing plate and the sealing portion in the present invention is applied to the viewing side portion of the liquid crystal display device.
  • the configuration is applied to the back side portion of the liquid crystal display device. It may be applied to both the viewing side portion and the back side portion of the liquid crystal display device, may be applied to an organic EL display device, and may be applied to a quantum dot display device.
  • the organic EL display device and the quantum dot display device can also employ configurations well known in the industry, and thus detailed description thereof is omitted.
  • Polarizing plate B-1 Polarizing Film
  • the polarizing film 21 is composed of a PVA resin film containing iodine as described above.
  • any appropriate resin can be adopted as the PVA resin for forming the PVA resin film.
  • Examples thereof include polyvinyl alcohol and ethylene-vinyl alcohol copolymer.
  • Polyvinyl alcohol is obtained by saponifying polyvinyl acetate.
  • the ethylene-vinyl alcohol copolymer can be obtained by saponifying an ethylene-vinyl acetate copolymer.
  • the degree of saponification of the PVA-based resin is usually 85 mol% to 100 mol%, preferably 95.0 mol% to 99.95 mol%, more preferably 99.0 mol% to 99.93 mol%. .
  • the degree of saponification can be determined according to JIS K 6726-1994. By using a PVA-based resin having such a saponification degree, a polarizing film having excellent durability can be obtained. If the degree of saponification is too high, there is a risk of gelation.
  • the average degree of polymerization of the PVA resin can be appropriately selected according to the purpose.
  • the average degree of polymerization is usually 1000 to 10000, preferably 1200 to 5000, and more preferably 1500 to 4500.
  • the average degree of polymerization can be determined according to JIS K 6726-1994.
  • the polarizing film contains iodine.
  • the polarizing film is substantially a PVA resin film in which iodine is adsorbed and oriented.
  • the iodine concentration in the PVA resin film is, for example, 5.0% by weight to 12.0% by weight.
  • the boric acid concentration in the PVA-based resin film is, for example, 12% by weight to 25% by weight.
  • the thickness of the PVA-based resin film is 8 ⁇ m or less as described above, preferably 7 ⁇ m or less, more preferably 6 ⁇ m or less.
  • the thickness of the PVA-based resin film is preferably 1.0 ⁇ m or more, more preferably 2.0 ⁇ m or more.
  • the polarizing film preferably exhibits absorption dichroism at any wavelength of 380 nm to 780 nm.
  • the single transmittance of the polarizing film is preferably 40.0% to 46.0%, more preferably 41.0% to 45.0%.
  • the polarization degree of the polarizing film is preferably 99.9% or more, more preferably 99.95% or more, and further preferably 99.98% or more.
  • the polarization degree of the polarizing film is preferably 90% or more, more preferably 93% or more, and still more preferably 95%. That's it.
  • the protective film 22 is comprised by arbitrary appropriate films which can be used as a protective film of a polarizing film.
  • the material as the main component of the film include cellulose resins such as triacetyl cellulose (TAC), polyester-based, polyvinyl alcohol-based, polycarbonate-based, polyamide-based, polyimide-based, polyethersulfone-based, and polysulfone-based materials.
  • transparent resins such as polystyrene, polynorbornene, polyolefin, (meth) acryl, and acetate.
  • thermosetting resins such as (meth) acrylic, urethane-based, (meth) acrylurethane-based, epoxy-based, and silicone-based or ultraviolet curable resins are also included.
  • a glassy polymer such as a siloxane polymer is also included.
  • a polymer film described in JP-A-2001-343529 (WO01 / 37007) can also be used.
  • a resin composition containing a thermoplastic resin having a substituted or unsubstituted imide group in the side chain and a thermoplastic resin having a substituted or unsubstituted phenyl group and nitrile group in the side chain for example, a resin composition having an alternating copolymer of isobutene and N-methylmaleimide and an acrylonitrile / styrene copolymer can be mentioned.
  • the polymer film can be, for example, an extruded product of the resin composition.
  • a resin substrate used in the production of a polarizing plate (described later in Section E) may be used as it is as a protective film.
  • the protective film may be subjected to a hard coat treatment or an antireflection treatment as necessary. Further, surface treatment such as anti-sticking treatment and anti-glare treatment may be applied.
  • the thickness of the protective film any appropriate thickness can be adopted as long as the effect of the present invention is obtained.
  • the thickness of the protective film is, for example, 20 ⁇ m to 40 ⁇ m, preferably 25 ⁇ m to 35 ⁇ m.
  • the thickness of the protective film is a thickness including the thickness of the surface treatment layer.
  • the inner protective film is preferably optically isotropic.
  • “optically isotropic” means that the in-plane retardation Re (550) is 0 nm to 10 nm and the thickness direction retardation Rth (550) is ⁇ 10 nm to +10 nm.
  • Re (550) of the inner protective film is preferably 0 nm to 8 nm, more preferably 0 nm to 6 nm, and further preferably 0 nm to 3 nm.
  • Rth (550) of the inner protective film is preferably ⁇ 8 nm to +8 nm, more preferably ⁇ 6 nm to +6 nm, and further preferably ⁇ 3 nm to +3 nm.
  • the sealing portion 30 covers the peripheral end surface of the polarizing plate 20, thereby maintaining the optical characteristics of the polarizing plate even in a humidified environment and improving the durability of the polarizing plate. Therefore, the sealing part preferably has a barrier function.
  • “having a barrier function” means that the amount of oxygen and / or water vapor penetrating the polarizing film is controlled to substantially block the polarizing film from these.
  • the sealing portion has a barrier property as described above, and typically has a barrier property against moisture and gas (for example, oxygen).
  • the water vapor transmission rate at 90% RH conditions is preferably not more than 300g / m 2 / 24hr, more preferably not more than 100g / m 2 / 24hr, more preferably is less 70g / m 2 / 24hr, most preferably not more than 40g / m 2 / 24hr.
  • the lower limit of the moisture permeability for example, 0.01g / m 2 / 24hr, and preferably below the detection limit. If the moisture permeability of the sealing part is in such a range, the polarizing film can be well protected from moisture and oxygen in the air.
  • the moisture permeability can be measured according to JIS Z0208.
  • the sealing portion can be made of any appropriate material as long as the above properties can be satisfied.
  • a typical example of the constituent material is an adhesive composition.
  • the “adhesive composition” is intended to include both an adhesive (adhesive composition) and an adhesive composition.
  • Examples of the pressure-sensitive adhesive composition include a rubber-based pressure-sensitive adhesive composition having a rubber-based polymer as a base polymer.
  • Examples of the rubber polymer include a conjugated diene polymer obtained by polymerizing one kind of conjugated diene compound, a conjugated diene copolymer obtained by polymerizing two or more kinds of conjugated diene compounds, and a conjugated diene.
  • Examples thereof include conjugated diene copolymers obtained by copolymerizing a compound and an aromatic vinyl compound, and hydrogenated products thereof.
  • the conjugated diene compound is not particularly limited as long as it is a monomer having a polymerizable conjugated diene.
  • Specific examples of the conjugated diene compound include 1,3-butadiene, isoprene, 2,3-dimethyl-1,3-butadiene, 1,3-pentadiene, 3-methyl-1,3-pentadiene, and 1,3-heptadiene. 1,3-hexadiene.
  • 1,3-butadiene and isoprene are preferable from the viewpoint of industrial availability.
  • Conjugated diene compounds may be used alone or in combination.
  • the aromatic vinyl compound is not particularly limited as long as it is a monomer having an aromatic vinyl structure copolymerizable with a conjugated diene compound.
  • Specific examples of the aromatic vinyl compound include styrene, p-methylstyrene, ⁇ -methylstyrene, vinylethylbenzene, vinylxylene, vinylnaphthalene, diphenylethylene and the like. Among these, styrene is preferable from the viewpoint of industrial availability.
  • Aromatic vinyl compounds may be used alone or in combination.
  • the diene copolymer may be a random copolymer or a block copolymer. Moreover, compounds other than a conjugated diene compound and an aromatic vinyl compound may be copolymerized to obtain a diene copolymer.
  • conjugated diene (co) polymers include butadiene rubber (BR), isoprene rubber (IR), styrene-butadiene copolymer (SBR), butadiene-isoprene-styrene random copolymer, isoprene.
  • BR butadiene rubber
  • IR isoprene rubber
  • SBR styrene-butadiene copolymer
  • SIS styrene-isoprene block copolymer
  • SEBS styrene-ethylene-butadiene block copolymer
  • NBR acrylonitrile-butadiene rubber
  • isoprene-styrene copolymers are preferred.
  • these hydrogenated materials can also be used suitably.
  • rubber polymers include isobutylene (IB), styrene-isobutylene-styrene block copolymer (SIBS), styrene-ethylenepropylene copolymer-styrene block copolymer, etc. Can also be used.
  • the rubber-based polymers may be used alone or in combination.
  • the rubber-based polymer that can be used in the present invention is preferably 50% by weight or more, more preferably 70% by weight or more, and still more preferably 80% by weight or more of the conjugated diene-based (co) polymer in the whole rubber-based polymer. Especially preferably, it contains 90% by weight or more.
  • the upper limit of the content of the conjugated diene (co) polymer is not particularly limited, and may be 100% by weight (that is, a rubber polymer composed only of the conjugated diene (co) polymer).
  • the pressure-sensitive adhesive composition contains a rubber-based polymer as a base polymer.
  • the content of the rubber-based polymer in the pressure-sensitive adhesive composition is preferably 40% by weight or more, more preferably 50% by weight or more, and further preferably 60% by weight or more.
  • the upper limit of content of a rubber-type polymer is not specifically limited, For example, it is 90 weight% or less.
  • the pressure-sensitive adhesive composition may further contain any appropriate additive in addition to the rubber-based polymer.
  • additives include cross-linking agents (for example, polyisocyanates, epoxy compounds, alkyl etherified melamine compounds), tackifiers (for example, rosin derivative resins, polyterpene resins, petroleum resins, oil-soluble phenol resins, vinyltoluenes). Resin), plasticizers, fillers (eg, layered silicates, clay materials, etc.), and anti-aging agents.
  • the kind, combination, addition amount, and the like of the additive added to the pressure-sensitive adhesive composition can be appropriately set according to the purpose.
  • the content (total amount) of the additive in the pressure-sensitive adhesive composition is preferably 60% by weight or less, more preferably 50% by weight or less, and still more preferably 40% by weight or less.
  • the adhesive composition typically include an active energy ray curable adhesive composition and a thermosetting adhesive composition.
  • the active energy ray curable adhesive composition include a light (for example, ultraviolet ray) curable adhesive composition and an electron beam curable adhesive composition.
  • the active energy ray curable adhesive composition can be selected as necessary, such as a radical curable type, a cationic curable type, and an anion curable type.
  • a radical curable type and a cationic curable type hybrid can be appropriately combined. It is also possible to use it.
  • the adhesive composition is an ultraviolet curable adhesive composition.
  • the ultraviolet curable adhesive composition for example, an adhesive composition described in JP2013-227419A can be suitably used. The description in this publication is incorporated herein by reference.
  • the thickness of the sealing portion is, for example, about 10 ⁇ m to 200 ⁇ m, preferably 15 ⁇ m to 100 ⁇ m, more preferably 20 ⁇ m to 70 ⁇ m, and further preferably 25 ⁇ m to 50 ⁇ m.
  • the “thickness of the sealing portion” is a thickness in a direction extending outward from the peripheral end surfaces of the polarizing film and the protective film unless otherwise specified.
  • the thickness of the sealing portion on the surface is, for example, about 10 ⁇ m to 200 ⁇ m, preferably 15 ⁇ m to 100 ⁇ m, more preferably Is 20 ⁇ m to 70 ⁇ m, more preferably 25 ⁇ m to 50 ⁇ m.
  • the pressure-sensitive adhesive layer 50 is composed of any appropriate pressure-sensitive adhesive.
  • a typical example of the pressure-sensitive adhesive is an acrylic pressure-sensitive adhesive.
  • the thickness of the pressure-sensitive adhesive layer is, for example, 20 ⁇ m to 100 ⁇ m.
  • the manufacturing method of the image display device of the present invention includes disposing a polarizing plate on one side of the display cell, forming a sealing portion so as to cover a peripheral end surface of the polarizing plate, and If necessary, a cover glass is disposed on the side opposite to the display cell of the polarizing plate.
  • a polarizing plate on one side of the display cell, forming a sealing portion so as to cover a peripheral end surface of the polarizing plate, and If necessary, a cover glass is disposed on the side opposite to the display cell of the polarizing plate.
  • a method for producing a polarizing plate according to one embodiment of the present invention typically comprises forming a PVA resin layer on one side of a resin substrate, and the resin substrate and the PVA resin. Stretching and dyeing the laminate with the layer to make the PVA-based resin layer a polarizing film.
  • a laminate of a resin base material and a PVA resin film may be produced, and the laminate may be dyed to use the PVA resin film as a polarizing film.
  • a single PVA resin film may be stretched and dyed to make the PVA resin film a polarizing film.
  • a PVA-type resin layer is formed by applying a coating solution containing a PVA-based resin on a resin base material and drying it.
  • thermoplastic resin any appropriate thermoplastic resin may be employed as the resin base material.
  • the thermoplastic resin include ester resins such as polyethylene terephthalate resins, cycloolefin resins such as norbornene resins, olefin resins such as polypropylene, polyamide resins, polycarbonate resins, and copolymer resins thereof. Is mentioned. Among these, preferred are norbornene resins and amorphous polyethylene terephthalate resins.
  • an amorphous (non-crystallized) polyethylene terephthalate resin is preferably used.
  • amorphous (hard to crystallize) polyethylene terephthalate resin is particularly preferably used.
  • Specific examples of the amorphous polyethylene terephthalate resin include a copolymer further containing isophthalic acid as a dicarboxylic acid, and a copolymer further containing cyclohexanedimethanol as a glycol.
  • the resin base material absorbs water, and the water can be plasticized by acting as a plasticizer. As a result, the stretching stress can be greatly reduced, the film can be stretched at a high magnification, and the stretchability can be superior to that during air stretching. As a result, a polarizing film having excellent optical characteristics can be produced.
  • the resin base material preferably has a water absorption rate of 0.2% or more, and more preferably 0.3% or more. On the other hand, the water absorption rate of the resin base material is preferably 3.0% or less, more preferably 1.0% or less.
  • the water absorption rate of the resin base material can be adjusted, for example, by introducing a modifying group into the forming material.
  • the water absorption is a value determined according to JIS K 7209.
  • the glass transition temperature (Tg) of the resin base material is preferably 170 ° C. or lower.
  • the stretchability of the laminate can be sufficiently ensured while suppressing crystallization of the PVA-based resin layer.
  • the temperature is more preferably 120 ° C. or lower.
  • the glass transition temperature of the resin substrate is preferably 60 ° C. or higher.
  • the PVA-based resin layer can be satisfactorily stretched at a suitable temperature (for example, about 60 ° C.).
  • a glass transition temperature lower than 60 ° C. may be used as long as the resin base material does not deform when applying and drying a coating solution containing a PVA-based resin.
  • the glass transition temperature of the resin substrate can be adjusted by, for example, heating using a crystallization material that introduces a modifying group into the forming material.
  • the glass transition temperature (Tg) is a value determined according to JIS K 7121.
  • the thickness of the resin base material before stretching is preferably 20 ⁇ m to 300 ⁇ m, more preferably 50 ⁇ m to 200 ⁇ m. If it is less than 20 ⁇ m, it may be difficult to form a PVA-based resin layer. If it exceeds 300 ⁇ m, for example, in stretching in water, it takes a long time for the resin base material to absorb water, and an excessive load may be required for stretching.
  • the coating solution is typically a solution obtained by dissolving the PVA resin in a solvent.
  • the solvent include water, dimethyl sulfoxide, dimethylformamide, dimethylacetamide, N-methylpyrrolidone, various glycols, polyhydric alcohols such as trimethylolpropane, and amines such as ethylenediamine and diethylenetriamine. These may be used alone or in combination of two or more. Among these, water is preferable.
  • the concentration of the PVA resin in the solution is preferably 3 to 20 parts by weight with respect to 100 parts by weight of the solvent. With such a resin concentration, a uniform coating film in close contact with the resin substrate can be formed.
  • Additives may be added to the coating solution.
  • the additive include a plasticizer and a surfactant.
  • the plasticizer include polyhydric alcohols such as ethylene glycol and glycerin.
  • the surfactant include nonionic surfactants. These can be used for the purpose of further improving the uniformity, dyeability and stretchability of the resulting PVA-based resin layer.
  • an easily bonding component is mentioned, for example. By using the easy-adhesion component, the adhesion between the resin base material and the PVA-based resin layer can be improved. As a result, for example, problems such as peeling of the PVA-based resin layer from the substrate can be suppressed, and dyeing and underwater stretching described later can be performed satisfactorily.
  • modified PVA such as acetoacetyl-modified PVA is used.
  • any appropriate method can be adopted as a coating method of the coating solution. Examples thereof include a roll coating method, a spin coating method, a wire bar coating method, a dip coating method, a die coating method, a curtain coating method, a spray coating method, a knife coating method (comma coating method and the like).
  • the coating / drying temperature of the coating solution is preferably 50 ° C. or higher.
  • the resin substrate Before forming the PVA-based resin layer, the resin substrate may be subjected to surface treatment (for example, corona treatment), or an easy-adhesion layer may be formed on the resin substrate. By performing such a treatment, the adhesion between the resin substrate and the PVA resin layer can be improved.
  • surface treatment for example, corona treatment
  • an easy-adhesion layer may be formed on the resin substrate.
  • the thickness of the PVA resin layer (before stretching) is preferably 3 ⁇ m to 20 ⁇ m.
  • any appropriate method can be adopted as a stretching method of the laminate. Specifically, it may be fixed end stretching or free end stretching (for example, a method of uniaxial stretching through a laminate between rolls having different peripheral speeds). Preferably, it is free end stretching.
  • the stretching direction of the laminate can be appropriately set. In one embodiment, it extends
  • the stretching method is not particularly limited, and may be an air stretching method or an underwater stretching method.
  • the underwater stretching method is preferable. According to the underwater stretching method, the resin base material and the PVA resin layer can be stretched at a temperature lower than the glass transition temperature (typically about 80 ° C.), and the crystallization of the PVA resin layer is suppressed. However, it can be stretched at a high magnification. As a result, a polarizing film having excellent optical characteristics can be produced.
  • the stretching of the laminate may be performed in one stage or in multiple stages.
  • the free end stretching and the fixed end stretching may be combined, or the underwater stretching method and the air stretching method may be combined.
  • the draw ratio (maximum draw ratio) of the laminated body mentioned later is a product of the draw ratio of each step.
  • the stretching temperature of the laminate can be set to any appropriate value depending on the resin base material, the stretching method, and the like.
  • the stretching temperature is preferably equal to or higher than the glass transition temperature (Tg) of the resin substrate, more preferably the glass transition temperature (Tg) of the resin substrate + 10 ° C., and particularly preferably Tg + 15 ° C. That's it.
  • the stretching temperature of the laminate is preferably 170 ° C. or lower.
  • the temperature of the stretching bath is 60 ° C. or higher, preferably 65 ° C. to 85 ° C., more preferably 65 ° C. to 75 ° C. If it is such temperature, it can extend
  • the glass transition temperature (Tg) of the resin base material is preferably 60 ° C. or higher in relation to the formation of the PVA-based resin layer.
  • the stretching temperature is lower than 60 ° C., there is a possibility that the stretching cannot be satisfactorily performed even in consideration of plasticization of the resin base material with water.
  • the higher the temperature of the stretching bath the higher the solubility of the PVA-based resin layer, and there is a possibility that excellent optical properties cannot be obtained.
  • the immersion time of the laminate in the stretching bath is preferably 15 seconds to 5 minutes.
  • the laminate When employing an underwater stretching method, it is preferable to stretch the laminate by immersing it in an aqueous boric acid solution (stretching in boric acid in water).
  • an aqueous boric acid solution as the stretching bath, the PVA resin layer can be provided with rigidity that can withstand the tension applied during stretching and water resistance that does not dissolve in water.
  • boric acid can form a tetrahydroxyborate anion in an aqueous solution and crosslink with a PVA resin by hydrogen bonding.
  • rigidity and water resistance can be imparted to the PVA-based resin layer, the film can be stretched satisfactorily, and a polarizing film having excellent optical properties can be produced.
  • the boric acid aqueous solution is preferably obtained by dissolving boric acid and / or borate in water as a solvent.
  • the boric acid concentration is 4.5 wt% or less, preferably 2.0 wt% to 4.5 wt%, more preferably 2.5 wt% to 4.0 wt%.
  • an aqueous solution obtained by dissolving a boron compound such as borax, glyoxal, glutaraldehyde, or the like in a solvent can also be used.
  • a dichroic substance typically iodine
  • an iodide is blended in the stretching bath (boric acid aqueous solution).
  • the iodide include potassium iodide, lithium iodide, sodium iodide, zinc iodide, aluminum iodide, lead iodide, copper iodide, barium iodide, calcium iodide, tin iodide, and titanium iodide.
  • the concentration of iodide is preferably 0.05 to 15 parts by weight, more preferably 0.5 to 8 parts by weight with respect to 100 parts by weight of water.
  • the draw ratio (maximum draw ratio) of the laminate is preferably 5.0 times or more with respect to the original length of the laminate. Such a high draw ratio can be achieved, for example, by employing an underwater drawing method (boric acid underwater drawing).
  • the “maximum stretch ratio” refers to a stretch ratio immediately before the laminate is ruptured. Separately, a stretch ratio at which the laminate is ruptured is confirmed, and a value that is 0.2 lower than that value. .
  • the laminate is stretched in air at a high temperature (for example, 95 ° C. or higher), and then stretched in boric acid in water and dyeing described later.
  • air stretching can be positioned as preliminary or auxiliary stretching for boric acid water stretching, and is hereinafter referred to as “air-assisted stretching”.
  • the laminate can be stretched at a higher magnification by combining air-assisted stretching.
  • a polarizing film having more excellent optical characteristics for example, the degree of polarization
  • the orientation of the resin base material is suppressed by combining the air auxiliary stretching and the boric acid water stretching rather than stretching by boric acid water stretching alone. While stretching.
  • the orientation of the resin base material is improved, the stretching tension increases, and stable stretching becomes difficult or breaks. Therefore, the laminate can be stretched at a higher magnification by stretching while suppressing the orientation of the resin substrate.
  • the orientation of the PVA-based resin can be improved, whereby the orientation of the PVA-based resin can be improved even after stretching in boric acid water.
  • the PVA resin is easily cross-linked with boric acid during boric acid water stretching, and boric acid is a nodal point. It is presumed that the orientation of the PVA-based resin is increased even after stretching in boric acid solution by being stretched in such a state. As a result, a polarizing film having excellent optical characteristics (for example, the degree of polarization) can be produced.
  • the stretching ratio in the air auxiliary stretching is preferably 3.5 times or less.
  • the stretching temperature of the air auxiliary stretching is preferably equal to or higher than the glass transition temperature of the PVA resin.
  • the stretching temperature is preferably 95 ° C to 150 ° C.
  • the maximum draw ratio in the case of combining the air auxiliary stretching and the boric acid solution stretching is preferably 5.0 times or more, more preferably 5.5 times or more, and further preferably, the original length of the laminate. Is 6.0 times or more.
  • the dyeing of the PVA resin layer is typically performed by adsorbing iodine to the PVA resin layer.
  • adsorption method for example, a method of immersing a PVA resin layer (laminate) in a staining solution containing iodine, a method of applying the staining solution to the PVA resin layer, and applying the staining solution to the PVA resin layer The method of spraying etc. are mentioned.
  • the PVA resin layer (laminate) is immersed in the dyeing solution. This is because iodine can be adsorbed well.
  • the staining solution is preferably an iodine aqueous solution.
  • the amount of iodine is preferably 0.1 to 0.5 parts by weight with respect to 100 parts by weight of water.
  • an iodide is added to the aqueous iodine solution. Specific examples of the iodide are as described above.
  • the blending amount of iodide is preferably 0.02 to 20 parts by weight, more preferably 0.1 to 10 parts by weight with respect to 100 parts by weight of water.
  • the liquid temperature during dyeing of the dyeing liquid is preferably 20 ° C. to 50 ° C. in order to suppress dissolution of the PVA resin.
  • the immersion time is preferably 5 seconds to 5 minutes in order to ensure the transmittance of the PVA resin layer.
  • the staining conditions concentration, liquid temperature, immersion time
  • immersion time is set so that the polarization degree of the polarizing film obtained may be 99.98% or more.
  • the immersion time is set so that the single transmittance of the obtained polarizing film is 40.0% to 42.5%.
  • the staining process can be performed at any appropriate timing.
  • it performs before an underwater extending
  • the PVA-based resin layer (laminate) can be appropriately subjected to treatments for forming a polarizing film.
  • the treatment for forming the polarizing film include insolubilization treatment, crosslinking treatment, washing treatment, and drying treatment.
  • count, order, etc. of these processes are not specifically limited.
  • the insolubilization treatment is typically performed by immersing a PVA resin layer (laminated body) in an aqueous boric acid solution.
  • a PVA resin layer laminated body
  • boric acid aqueous solution preferably 1 to 4 parts by weight with respect to 100 parts by weight of water.
  • the liquid temperature of the insolubilizing bath (boric acid aqueous solution) is preferably 20 ° C. to 50 ° C.
  • the insolubilization treatment is performed before the above-described underwater stretching or the above-described dyeing treatment.
  • the cross-linking treatment is typically performed by immersing a PVA resin layer (laminated body) in an aqueous boric acid solution.
  • the concentration of the boric acid aqueous solution is preferably 1 to 5 parts by weight with respect to 100 parts by weight of water.
  • blend an iodide it is preferable to mix
  • the blending amount of iodide is preferably 1 to 5 parts by weight with respect to 100 parts by weight of water.
  • the liquid temperature of the crosslinking bath is preferably 20 ° C. to 60 ° C.
  • the crosslinking treatment is performed before the underwater stretching. In a preferred embodiment, air stretching, dyeing treatment and crosslinking treatment are performed in this order.
  • the above-described cleaning treatment is typically performed by immersing the PVA resin layer (laminated body) in a potassium iodide aqueous solution.
  • the drying temperature in the drying treatment is preferably 30 ° C. to 100 ° C.
  • the polarizing film is formed on the resin base material.
  • the laminate of the resin base material and the polarizing film obtained in the above section E-1 is arranged as the polarizing plate 20 on the viewing side of the liquid crystal cell 10.
  • a protective film is bonded to the polarizing film surface of a laminate of a resin base material (protective film) and a polarizing film (for convenience, this protective film is referred to as another protective film).
  • a laminate of the obtained resin substrate (protective film) / polarizing film / another protective film is disposed on the viewing side of the liquid crystal cell 10 as the polarizing plate 20.
  • a protective film is bonded to the surface of the polarizing film of the laminate of the resin base material and the polarizing film, and then the resin base material is peeled and removed.
  • the obtained polarizing film / protective film laminate is disposed on the viewing side of the liquid crystal cell 10 as the polarizing plate 20.
  • another protective film is bonded to the polarizing film surface (resin substrate peeling surface) of the polarizing film / protective film laminate, and the protective film / polarizing film / other protective film The laminate is disposed on the viewing side of the liquid crystal cell 10 as the polarizing plate 20.
  • the polarizing plate 20 is bonded to the liquid crystal cell 10 (substantially, the viewing side substrate of the liquid crystal cell) via the adhesive layer 50. Further, as shown in FIG. 3A, the size of the polarizing plate 20 is typically smaller than the size of the liquid crystal cell 10.
  • the sealing part is formed so as to cover the peripheral end face of the polarizing plate 20 arranged in the liquid crystal cell 10.
  • the case where a sealing part is formed with an adhesive composition is demonstrated.
  • the sealing part is typically formed by disposing the adhesive composition so as to cover the outer peripheral end face of the laminate.
  • the sealing portion may be formed by applying and curing a liquid (before curing) adhesive composition at a predetermined position, and placing the sheet-like pressure-sensitive adhesive composition at a predetermined position (typically, It may be formed by bonding).
  • seat which has a size larger than a polarizing plate is arrange
  • the length of the extending portion of the sheet can be set so as to finally cover the entire peripheral end face of the polarizing plate.
  • the extending portion of the sheet can hang down by its own weight and cover the peripheral end surface of the polarizing plate by adjusting the softness (for example, elastic modulus) of the sheet. Or you may bend the extension part of a sheet
  • a sealing portion that covers the entire surface of the polarizing plate opposite to the display cell and the entire peripheral end surface is formed.
  • a cover glass 40 is disposed on the opposite side of the polarizing plate 20 from the liquid crystal cell 10.
  • the cover glass 40 is bonded to the polarizing plate 20 via a sealing portion 30 that covers the surface of the polarizing plate 20 opposite to the liquid crystal cell 10.
  • a back side polarizing plate and a back side optical member are laminated and a backlight part (if present) is incorporated by a procedure well known in the industry. In this way, a liquid crystal display device can be obtained.
  • the above embodiment is an example.
  • a similar procedure may be adopted for the back side portion of the liquid crystal display device; a well-known procedure is adopted for the viewing side portion of the liquid crystal display device, and the same procedure is adopted only for the back side portion of the liquid crystal display device.
  • a similar procedure may be adopted for the organic EL display device; a similar procedure may be adopted for the quantum dot display device.
  • the present invention will be specifically described by way of examples, but the present invention is not limited to these examples.
  • the measuring method of each characteristic is as follows.
  • a pressure-sensitive adhesive sheet having a thickness of 50 ⁇ m was formed using the pressure-sensitive adhesive compositions prepared in Examples and Comparative Examples according to the methods described in the Examples.
  • One release liner of the pressure-sensitive adhesive sheet is peeled off to expose the pressure-sensitive adhesive surface, and the pressure-sensitive adhesive sheet is bonded to a triacetyl cellulose film (TAC film, thickness: 25 ⁇ m, manufactured by Konica Minolta Co., Ltd.) via the pressure-sensitive adhesive surface. Cut out into a circle. Finally, the other release liner was peeled off to obtain a measurement sample.
  • TAC film triacetyl cellulose film, thickness: 25 ⁇ m, manufactured by Konica Minolta Co., Ltd.
  • the water vapor transmission rate (water vapor transmission rate) was measured by the water vapor transmission test method (a cup method, according to JIS Z 0208).
  • the measurement conditions were as follows.
  • a constant temperature and humidity chamber was used for the measurement.
  • Color loss amount From the polarizing plates used in the examples and comparative examples, a test piece (50 mm ⁇ 50 mm) having two sides facing each other in the direction perpendicular to the stretching direction and the stretching direction was cut out. The test piece was bonded to an alkali-free glass plate with an adhesive.
  • sealing portions were formed in the same manner as in the production of the liquid crystal display devices of the respective examples and comparative examples, and liquid crystal display device substitutes were produced.
  • this was left in an oven at 85 ° C. and 85% RH for 120 hours to be humidified and placed in a state of crossed Nicols with a standard polarizing plate, the state of color loss at the end of the polarizing film after humidification was examined with a microscope. It was. Specifically, the magnitude of color loss from the edge of the polarizing film (color loss amount: ⁇ m) was measured. Using Olympus MX61L as a microscope, the amount of color loss was measured from an image taken at a magnification of 10 times. As shown in FIG.
  • the larger one of the color loss amount a from the end portion in the stretching direction and the color loss amount b from the end portion in the direction orthogonal to the stretching direction was defined as the color loss amount.
  • the pressure-sensitive adhesive was cut into 50 mm ⁇ 50 mm. It bonded together on the 100 mm x 100 mm non-alkali glass surface through the layer.
  • the sheet-like pressure-sensitive adhesives used in Examples and Comparative Examples were disposed on the surface of the polarizing plate opposite to the alkali-free glass.
  • the sheet was arranged so as to extend from all four sides constituting the outer periphery of the polarizing plate.
  • the length of the four extending portions was 5 mm each.
  • the sheet hangs down due to its own weight and directly adheres to the glass, covering the outer peripheral end face of the polarizing plate and sealing.
  • the sealing part which covers the whole surface of a polarizing plate and the whole outer peripheral end surface was formed.
  • the cover glass (thickness 1 mm) was bonded together through the sealing part (adhesive).
  • a similar polarizing plate was bonded to the back side of the glass via an acrylic pressure-sensitive adhesive layer (thickness: 25 ⁇ m). In this way, an alternative liquid crystal display device was produced.
  • Example 1 As a resin base material, an amorphous polyethylene terephthalate (IPA copolymerized PET) film having a thickness of 100 ⁇ m and a Tg of 75 ° C. isophthalic acid unit of 7 mol% was prepared. The surface of this film was subjected to corona treatment (58 W / m2 / min).
  • IPA copolymerized PET amorphous polyethylene terephthalate
  • Acetoacetyl-modified PVA manufactured by Nippon Synthetic Chemical Industry Co., Ltd., trade name: Gohsephimer Z200, average polymerization degree: 1200, saponification degree: 98.5 mol% or more, acetoacetylation degree: 5%
  • PVA average PVA resin having a polymerization ratio of 4200 and a saponification degree of 99.2 mol% in a ratio of 1: 9 is prepared, and 13 parts by weight of potassium iodide is added to 100 parts by weight of the PVA resin.
  • a PVA-based resin aqueous solution was prepared (PVA-based resin concentration: 5.5% by weight).
  • This aqueous solution is applied to the corona-treated surface of the resin substrate so that the film thickness after drying is 13 ⁇ m, and dried for 10 minutes by hot air drying in an atmosphere of 60 ° C., and the PVA system having a thickness of 9 ⁇ m is formed on the resin substrate. A resin layer was formed. In this way, a laminate was produced. The obtained laminate was stretched 2.4 times in air at 140 ° C. (air-assisted stretching). Next, the laminate was immersed in an aqueous boric acid solution having a liquid temperature of 30 ° C. for 30 seconds to insolubilize the PVA resin layer. The boric acid aqueous solution in this step had a boric acid content of 3 parts by weight with respect to 100 parts by weight of water.
  • the laminate was dyed in a staining solution containing iodine and potassium iodide at a liquid temperature of 30 ° C. for an arbitrary time so that the single transmittance of the obtained polarizing film was about 42 to 45%.
  • the staining solution uses water as a solvent, iodine concentration in the range of 0.1 to 0.4% by weight, potassium iodide concentration in the range of 0.7 to 2.8% by weight, iodine and potassium iodide.
  • the concentration ratio was 1: 7.
  • the laminate was immersed in an aqueous boric acid solution at 30 ° C. for 60 seconds, and the PVA resin layer on which iodine was adsorbed was subjected to crosslinking treatment.
  • the boric acid aqueous solution in this step had a boric acid content of 3 parts by weight with respect to 100 parts by weight of water and a potassium iodide content of 3 parts by weight with respect to 100 parts by weight of water. Further, the laminate was stretched 2.3 times in a boric acid aqueous solution at a stretching temperature of 70 ° C. in the same direction as the previous air-assisted stretching (final draw ratio: 5.50 times).
  • the boric acid aqueous solution in this step had a boric acid content of 3.5 parts by weight with respect to 100 parts by weight of water and a potassium iodide content of 5 parts by weight with respect to 100 parts by weight of water.
  • the laminate is washed with an aqueous solution having a potassium iodide content of 4 parts by weight with respect to 100 parts by weight of water and dried with hot air at 60 ° C. to obtain a polarizing film having a thickness of 5 ⁇ m on the resin substrate. It was.
  • a cycloolefin film (manufactured by Nippon Zeon Co., Ltd., ZF-12, 13 ⁇ m) was bonded to the surface of the obtained polarizing film (surface opposite to the resin substrate) via a curable adhesive. Specifically, a curable adhesive was applied to each of the polarizing film and the cycloolefin-based film so as to have a thickness of 1.0 ⁇ m, and bonded using a roll machine. Thereafter, visible light was irradiated from the cycloolefin film side to cure the curable adhesive.
  • a liquid crystal panel was taken out from an IPS mode liquid crystal display device (product name “iPad (registered trademark) Air” manufactured by Apple), an optical member such as a polarizing plate was removed from the liquid crystal panel, and a liquid crystal cell was taken out.
  • the liquid crystal cell was used by washing and cleaning both surfaces (outside of each glass substrate) with alcohol.
  • a sheet-like adhesive moisture permeability: 24g / m 2 / 24hr, thickness: 25 [mu] m
  • the sheet was arranged so as to extend from all four sides constituting the outer periphery of the polarizing plate.
  • the length of the four extending portions was 5 mm each.
  • the sheet hangs down due to its own weight, directly adheres to the liquid crystal cell, covers the outer peripheral end face of the polarizing plate, and is sealed.
  • the sealing part which covers the whole surface on the opposite side to the liquid crystal cell of a polarizing plate and the whole outer peripheral end surface was formed.
  • the pressure-sensitive adhesive constituting the sealing part is based on 100 parts by weight of styrene / ethylene propylene copolymer / styrene block copolymer (manufactured by Kuraray, trade name “Septon 2063”, styrene content: 13% by weight).
  • liquid crystal display device substitute (4) above was subjected to evaluation of color loss, light leakage, and white blur, color loss, light leakage, white blur after 120 hours in an environment of 85 ° C. and 85% RH. It was confirmed that the black display was satisfactory.
  • Example 2 Moisture permeability was produced except for forming a seal with 6g / m 2 / 24hr at which the pressure-sensitive adhesive (thickness 100 [mu] m) in the same manner as in Example 1 liquid crystal display device and replacement.
  • the liquid crystal display device substitute (3) was subjected to the evaluation of the amount of color loss in the same manner as in Example 1. The results are shown in Table 1. Further, when the liquid crystal display device substitute of (4) was subjected to evaluation of color loss, light leakage and white blur in the same manner as in Example 1, after being placed in an environment of 85 ° C. and 85% RH for 120 hours. It was confirmed that the black display had no color loss, light leakage, or white blur.
  • Example 3 Moisture permeability to produce a liquid crystal display device and alternatives except for forming a seal with a 12g / m 2 / 24hr at which the pressure-sensitive adhesive (thickness 50 [mu] m) in the same manner as in Example 1.
  • the liquid crystal display device substitute (3) was subjected to the evaluation of the amount of color loss in the same manner as in Example 1. The results are shown in Table 1. Further, when the liquid crystal display device substitute of (4) was subjected to evaluation of color loss, light leakage and white blur in the same manner as in Example 1, after being placed in an environment of 85 ° C. and 85% RH for 120 hours. It was confirmed that the black display had no color loss, light leakage, or white blur.
  • Example 4 A liquid crystal display device and an alternative were produced in the same manner as in Example 2 except that the cover glass was not disposed.
  • the liquid crystal display device substitute (3) was subjected to the evaluation of the amount of color loss in the same manner as in Example 1. The results are shown in Table 1. Further, when the liquid crystal display device substitute of (4) was subjected to evaluation of color loss, light leakage and white blur in the same manner as in Example 1, after being placed in an environment of 85 ° C. and 85% RH for 120 hours. It was confirmed that the black display had no color loss, light leakage, or white blur.
  • Example 5 In the same manner as in Example 1, a laminate having a configuration of polarizing film / cycloolefin film (protective film) was obtained.
  • a cycloolefin film (manufactured by Nippon Zeon Co., Ltd., ZD-12, 23 ⁇ m) is bonded to the polarizing film surface of the laminate through a curable adhesive, and a protective film (ZD-12) / polarizing film / protective film ( A polarizing plate having the configuration of ZF-12) was obtained.
  • a liquid crystal display device and an alternative were prepared in the same manner as in Example 3 except that an acrylic adhesive was formed on the surface of the protective film (ZF-12) for the polarizing plate.
  • the liquid crystal display device substitute (3) was subjected to the evaluation of the amount of color loss in the same manner as in Example 1. The results are shown in Table 1. Further, when the liquid crystal display device substitute of (4) was subjected to evaluation of color loss, light leakage and white blur in the same manner as in Example 1, after being placed in an environment of 85 ° C. and 85% RH for 120 hours. It was confirmed that the black display had no color loss, light leakage, or white blur.
  • Example 6 While immersing a PVA resin film (manufactured by Kuraray Co., Ltd., trade name “PE-6000”, thickness: 60 ⁇ m, average polymerization degree: 2,400, saponification degree: 99.9 mol%) in a 30 ° C. water bath for 1 minute. Film stretched 1.2 times in the conveying direction, then dipped in a 30 ° C. aqueous solution with an iodine concentration of 0.04% by weight and a potassium concentration of 0.3% by weight, but not stretched at all (original length) The film was stretched 2 times based on the above. Next, this stretched film was further stretched up to 3 times based on the original length while being immersed in an aqueous solution at 30 ° C.
  • a PVA resin film manufactured by Kuraray Co., Ltd., trade name “PE-6000”, thickness: 60 ⁇ m, average polymerization degree: 2,400, saponification degree: 99.9 mol%
  • a PVA-based resin aqueous solution (manufactured by Nippon Synthetic Chemical Industry Co., Ltd., trade name “GOHSEFIMAR (registered trademark) Z-200”, resin concentration: 3% by weight) is applied to both surfaces of the polarizing film, and a cycloolefin film (Zeonor, Zeonor ZF14, thickness: 13 ⁇ m) and a triacetylcellulose film (Konica Minolta, KC4UY) were bonded together and heated in an oven maintained at 60 ° C. for 5 minutes to obtain a polarizing plate. . Subsequent procedures were performed in the same manner as in Example 2 to produce a liquid crystal display device and an alternative.
  • a cycloolefin film Zeonor, Zeonor ZF14, thickness: 13 ⁇ m
  • a triacetylcellulose film Konica Minolta, KC4UY
  • the liquid crystal display device substitute (3) was subjected to the evaluation of the amount of color loss in the same manner as in Example 1. The results are shown in Table 1. Further, when the liquid crystal display device substitute of (4) was subjected to evaluation of color loss, light leakage and white blur in the same manner as in Example 1, after being placed in an environment of 85 ° C. and 85% RH for 120 hours. It was confirmed that the black display had no color loss, light leakage, or white blur.
  • Example 7 A smartphone (Galaxy-S5) manufactured by Samsung Radio Co., Ltd., in which a polarizing plate is used for antireflection, was disassembled and an organic EL display device was taken out. The polarizing plate attached to the organic EL display device was peeled and removed, and the surface from which the polarizing plate was removed was washed. The removal surface was bonded to the polarizing plate used in Example 3 (a sealing portion was formed and placed in an environment of 85 ° C. and 85% RH for 120 hours) to obtain an organic EL display device. When the obtained organic EL display device was displayed in black, it was confirmed that it was a good black display free from color loss, light leakage, and white blur.
  • 3-glycidoxypropyltrimethoxysilane (trade name: KBM403, manufactured by Shin-Etsu Chemical Co., Ltd.) is used as a silane coupling agent for 100 parts of the solid content of the polymer.
  • trimethylolpropane adduct of xylylene diisocyanate (trade name: Takenate D110N, manufactured by Mitsui Chemicals, Inc.) as a crosslinking agent, these were mixed uniformly.
  • An acrylic pressure-sensitive adhesive was prepared.
  • the moisture permeability of the resultant pressure-sensitive adhesive was greater than 1000g / m 2 / 24hr.
  • a liquid crystal display device and an alternative were produced in the same manner as in Example 1 except that the sealing portion was formed using this adhesive.
  • the liquid crystal display device substitute (3) was subjected to the evaluation of the amount of color loss in the same manner as in Example 1. The results are shown in Table 1. Moreover, when the liquid crystal display device substitute of (4) was subjected to evaluation of color loss, light leakage and white blur in the same manner as in Example 1, light leakage due to color loss of the polarizing plate was confirmed.
  • Example 2 Example except that the sealing part was formed only on the surface opposite to the liquid crystal cell of the polarizing plate using the same size sheet-like adhesive as the polarizing plate (that is, the peripheral end face of the polarizing plate was not covered).
  • a liquid crystal display device and an alternative were produced.
  • the liquid crystal display device substitute (3) was subjected to the evaluation of the amount of color loss in the same manner as in Example 1. The results are shown in Table 1.
  • the liquid crystal display device substitute of (4) was subjected to evaluation of color loss, light leakage and white blur in the same manner as in Example 1, light leakage due to color loss of the polarizing plate was confirmed.
  • Example 4 A liquid crystal display device and an alternative were produced in the same manner as in Example 1 except that the sealing portion was not formed and the cover glass was not disposed.
  • the liquid crystal display device substitute (3) was subjected to the evaluation of the amount of color loss in the same manner as in Example 1. The results are shown in Table 1.
  • the liquid crystal display device substitute of (4) was subjected to evaluation of color loss, light leakage and white blur in the same manner as in Example 1, light leakage due to color loss of the polarizing plate was confirmed.
  • the image display device of the present invention is suitably used for televisions, mobile phones, digital cameras, video cameras, portable game machines, car navigation systems, copy machines, printers, fax machines, watches, microwave ovens, and the like.

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  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Nonlinear Science (AREA)
  • Optics & Photonics (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Mathematical Physics (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Theoretical Computer Science (AREA)
  • Manufacturing & Machinery (AREA)
  • Polarising Elements (AREA)
  • Liquid Crystal (AREA)
  • Electroluminescent Light Sources (AREA)
  • Devices For Indicating Variable Information By Combining Individual Elements (AREA)

Abstract

L'invention concerne un dispositif d'affichage d'image capable de conserver d'excellentes propriétés optiques même dans un environnement humide, et d'empêcher ainsi la décoloration. Le dispositif d'affichage d'image de l'invention comprend : une cellule d'affichage (10) ; une plaque polarisante (20) disposée sur au moins un côté de la cellule d'affichage (10) ; et une partie d'étanchéité (30) recouvrant les surfaces d'extrémité périphériques de la plaque polarisante (30). La plaque polarisante (20) comprend un film polarisant (21) constitué d'un film de résine à base d'alcool polyvinylique contenant de l'iode, et la perméabilité à l'humidité de la partie d'étanchéité (30) est de 300 g/m2/24h ou moins. Dans un mode de réalisation, le dispositif d'affichage d'image comprend une quantité décolorée de 100 µm ou moins après avoir été maintenu pendant 120 heures dans un environnement à 85 °C et 85 % de HR.
PCT/JP2018/005906 2017-02-28 2018-02-20 Dispositif d'affichage d'image et procédé de fabrication dudit dispositif d'affichage d'image Ceased WO2018159377A1 (fr)

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CN201880013947.2A CN110326036A (zh) 2017-02-28 2018-02-20 图像显示装置及该图像显示装置的制造方法
JP2019502895A JPWO2018159377A1 (ja) 2017-02-28 2018-02-20 画像表示装置および該画像表示装置の製造方法

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110208892A (zh) * 2019-05-29 2019-09-06 昆山维信诺科技有限公司 偏光片及其制备方法、显示面板
JP2023067895A (ja) * 2021-07-29 2023-05-16 日東電工株式会社 光学積層体

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP7599854B2 (ja) * 2020-07-03 2024-12-16 住友化学株式会社 粘着剤層付き偏光板

Citations (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS55138715A (en) * 1979-04-18 1980-10-29 Hitachi Ltd Liquid crystal display element
JPS58133128U (ja) * 1983-01-13 1983-09-08 セイコーエプソン株式会社 液晶表示体
JPH0413981U (fr) * 1990-05-25 1992-02-04
JP2008152025A (ja) * 2006-12-18 2008-07-03 Topcon Corp 偏光板の防湿コーティング方法及びその方法により製造された偏光板
US20100221455A1 (en) * 2009-02-25 2010-09-02 Lg Chem, Ltd. Composition for primer coating, optical film comprising the same, and polarizing plate comprising the same
JP2015172740A (ja) * 2014-02-18 2015-10-01 日東電工株式会社 積層体および画像表示装置
JP2016170412A (ja) * 2015-03-12 2016-09-23 日東電工株式会社 偏光フィルムおよびその製造方法、光学フィルムならびに画像表示装置
WO2017010225A1 (fr) * 2015-07-13 2017-01-19 日東電工株式会社 Composition adhésive durcissable pour film polarisant, film polarisant, procédé de fabrication pour ledit film polarisant, film optique, et dispositif d'affichage d'image
JP2017032676A (ja) * 2015-07-30 2017-02-09 住友化学株式会社 光学積層体及び液晶表示装置
JP2017082026A (ja) * 2015-10-22 2017-05-18 積水化学工業株式会社 接着剤組成物及び偏光板
JP2017210504A (ja) * 2016-05-23 2017-11-30 積水化学工業株式会社 表示素子用封止剤及び表示素子

Family Cites Families (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6083903A (ja) * 1983-10-14 1985-05-13 Hitachi Ltd 偏光素子及びそれを用いた液晶電気光学デバイス
JP3165168B2 (ja) * 1991-04-02 2001-05-14 日東電工株式会社 偏光板及び液晶表示装置
JP3004782B2 (ja) * 1991-08-14 2000-01-31 日東電工株式会社 偏光板及び液晶表示装置
JP4279944B2 (ja) 1999-06-01 2009-06-17 株式会社サンリッツ 偏光板の製造方法
JP4218941B2 (ja) * 2003-02-25 2009-02-04 日東電工株式会社 光学部材、その製造方法、粘着型光学部材および画像表示装置
WO2007105485A1 (fr) * 2006-03-10 2007-09-20 Nippon Shokubai Co., Ltd. Film de protection pour polariseur, plaque polarisante et affichage d'image
CN101122647A (zh) * 2006-08-08 2008-02-13 住友化学株式会社 偏振片及其制造方法
KR20080013752A (ko) * 2006-08-08 2008-02-13 스미또모 가가꾸 가부시끼가이샤 편광 시트 및 편광 시트 제조 방법
JP2009009100A (ja) * 2007-05-31 2009-01-15 Sumitomo Chemical Co Ltd 偏光板
JP2010117537A (ja) * 2008-11-13 2010-05-27 Sumitomo Chemical Co Ltd 偏光板及びそれを用いた投射型液晶表示装置
JP2010191203A (ja) * 2009-02-18 2010-09-02 Sumitomo Chemical Co Ltd 偏光板の製造方法
JP2010243863A (ja) * 2009-04-08 2010-10-28 Sony Corp 偏光板及び光装置
JP2011022202A (ja) * 2009-07-13 2011-02-03 Sumitomo Chemical Co Ltd 偏光板およびそれを用いた画像表示装置
JP2011033970A (ja) * 2009-08-05 2011-02-17 Sumitomo Chemical Co Ltd 偏光板およびその製造方法、ならびに投射型液晶表示装置
JP5701127B2 (ja) * 2010-04-05 2015-04-15 リンテック株式会社 粘着性組成物および該組成物から得られる粘着性シート
JP2013242395A (ja) * 2012-05-18 2013-12-05 Japan Display Inc 液晶表示装置
KR101433571B1 (ko) * 2013-01-24 2014-08-27 엘지디스플레이 주식회사 액정 표시 장치
KR20150119024A (ko) * 2013-03-12 2015-10-23 코니카 미놀타 가부시키가이샤 유기 일렉트로루미네센스 표시 장치 및 그 제조 방법
KR102102351B1 (ko) * 2013-04-25 2020-04-21 삼성디스플레이 주식회사 기능성 편광 필름 및 이를 채용하는 유기발광표시장치.
JP6152319B2 (ja) * 2013-08-09 2017-06-21 日東電工株式会社 粘着剤組成物、粘着テープ又はシート
JP6150428B2 (ja) * 2013-08-12 2017-06-21 日東電工株式会社 偏光膜、偏光膜を含む光学機能フィルム積層体、及び、偏光膜を含む光学フィルム積層体の製造方法、並びに偏光膜を有する有機ｅｌ表示装置
KR102079544B1 (ko) * 2013-08-30 2020-02-21 엘지디스플레이 주식회사 면 봉지 방식의 유기발광 다이오드 표시장치
JP6138002B2 (ja) * 2013-09-09 2017-05-31 日東電工株式会社 透明導電膜用粘着剤層付偏光フィルム、積層体、及び、画像表示装置
KR102096980B1 (ko) * 2015-01-26 2020-04-03 동우 화인켐 주식회사 편광판 및 이를 포함하는 화상 표시 장치
KR101822254B1 (ko) * 2015-02-04 2018-01-25 주식회사 엘지화학 점착제 조성물
CN205027996U (zh) * 2015-09-24 2016-02-10 湖北优利迪显示科技有限公司 一种新型lcd模组

Patent Citations (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS55138715A (en) * 1979-04-18 1980-10-29 Hitachi Ltd Liquid crystal display element
JPS58133128U (ja) * 1983-01-13 1983-09-08 セイコーエプソン株式会社 液晶表示体
JPH0413981U (fr) * 1990-05-25 1992-02-04
JP2008152025A (ja) * 2006-12-18 2008-07-03 Topcon Corp 偏光板の防湿コーティング方法及びその方法により製造された偏光板
US20100221455A1 (en) * 2009-02-25 2010-09-02 Lg Chem, Ltd. Composition for primer coating, optical film comprising the same, and polarizing plate comprising the same
JP2015172740A (ja) * 2014-02-18 2015-10-01 日東電工株式会社 積層体および画像表示装置
JP2016170412A (ja) * 2015-03-12 2016-09-23 日東電工株式会社 偏光フィルムおよびその製造方法、光学フィルムならびに画像表示装置
WO2017010225A1 (fr) * 2015-07-13 2017-01-19 日東電工株式会社 Composition adhésive durcissable pour film polarisant, film polarisant, procédé de fabrication pour ledit film polarisant, film optique, et dispositif d'affichage d'image
JP2017032676A (ja) * 2015-07-30 2017-02-09 住友化学株式会社 光学積層体及び液晶表示装置
JP2017082026A (ja) * 2015-10-22 2017-05-18 積水化学工業株式会社 接着剤組成物及び偏光板
JP2017210504A (ja) * 2016-05-23 2017-11-30 積水化学工業株式会社 表示素子用封止剤及び表示素子

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110208892A (zh) * 2019-05-29 2019-09-06 昆山维信诺科技有限公司 偏光片及其制备方法、显示面板
CN110208892B (zh) * 2019-05-29 2021-06-15 苏州清越光电科技股份有限公司 偏光片及其制备方法、显示面板
JP2023067895A (ja) * 2021-07-29 2023-05-16 日東電工株式会社 光学積層体
JP7557561B2 (ja) 2021-07-29 2024-09-27 日東電工株式会社 光学積層体

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TW201837579A (zh) 2018-10-16
TWI690760B (zh) 2020-04-11

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