WO2017170216A1 - 液晶表示装置 - Google Patents

液晶表示装置 Download PDF

Info

Publication number
WO2017170216A1
WO2017170216A1 PCT/JP2017/011981 JP2017011981W WO2017170216A1 WO 2017170216 A1 WO2017170216 A1 WO 2017170216A1 JP 2017011981 W JP2017011981 W JP 2017011981W WO 2017170216 A1 WO2017170216 A1 WO 2017170216A1
Authority
WO
WIPO (PCT)
Prior art keywords
liquid crystal
display device
crystal display
film
polarizer
Prior art date
Application number
PCT/JP2017/011981
Other languages
English (en)
French (fr)
Japanese (ja)
Inventor
敦史 藤田
村田 浩一
佐々木 靖
Original Assignee
東洋紡株式会社
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=59965538&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=WO2017170216(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by 東洋紡株式会社 filed Critical 東洋紡株式会社
Priority to CN202010291214.4A priority Critical patent/CN111443417B/zh
Priority to CN201780021586.1A priority patent/CN109073929B/zh
Priority to KR1020207010384A priority patent/KR102311948B1/ko
Priority to KR1020187030586A priority patent/KR102312023B1/ko
Priority to JP2017531407A priority patent/JP6205089B1/ja
Priority to KR1020217032059A priority patent/KR102502207B1/ko
Publication of WO2017170216A1 publication Critical patent/WO2017170216A1/ja

Links

Classifications

    • GPHYSICS
    • G02OPTICS
    • G02BOPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B5/00Optical elements other than lenses
    • G02B5/30Polarising elements
    • G02B5/3025Polarisers, i.e. arrangements capable of producing a definite output polarisation state from an unpolarised input state
    • G02B5/3033Polarisers, 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
    • GPHYSICS
    • G02OPTICS
    • G02FOPTICAL 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
    • G02F1/00Devices 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
    • G02F1/01Devices 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 
    • G02F1/13Devices 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
    • G02F1/133Constructional arrangements; Operation of liquid crystal cells; Circuit arrangements
    • G02F1/1333Constructional arrangements; Manufacturing methods
    • G02F1/1335Structural association of cells with optical devices, e.g. polarisers or reflectors
    • G02F1/133528Polarisers
    • GPHYSICS
    • G02OPTICS
    • G02BOPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B5/00Optical elements other than lenses
    • G02B5/30Polarising elements
    • GPHYSICS
    • G02OPTICS
    • G02BOPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B1/00Optical elements characterised by the material of which they are made; Optical coatings for optical elements
    • G02B1/10Optical coatings produced by application to, or surface treatment of, optical elements
    • G02B1/14Protective coatings, e.g. hard coatings
    • GPHYSICS
    • G02OPTICS
    • G02FOPTICAL 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
    • G02F1/00Devices 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
    • G02F1/01Devices 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 
    • G02F1/13Devices 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
    • G02F1/133Constructional arrangements; Operation of liquid crystal cells; Circuit arrangements
    • G02F1/1333Constructional arrangements; Manufacturing methods
    • G02F1/1335Structural association of cells with optical devices, e.g. polarisers or reflectors
    • GPHYSICS
    • G02OPTICS
    • G02FOPTICAL 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
    • G02F1/00Devices 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
    • G02F1/01Devices 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 
    • G02F1/13Devices 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
    • G02F1/133Constructional arrangements; Operation of liquid crystal cells; Circuit arrangements
    • G02F1/1333Constructional arrangements; Manufacturing methods
    • G02F1/1335Structural association of cells with optical devices, e.g. polarisers or reflectors
    • G02F1/133528Polarisers
    • G02F1/133531Polarisers characterised by the arrangement of polariser or analyser axes

Definitions

  • the present invention relates to a liquid crystal display device used for a monitor for a personal computer, a television and the like.
  • Patent Document 1 discloses a viewing side and a backlight arranged above and below a liquid crystal cell of a liquid crystal display device.
  • Patent Document 2 pays attention to the difference in contraction force between the absorption axis direction and the transmission axis direction of the polarizing plate, and warps the display device by reducing the contraction force of the polarizing plate in the main contraction direction at high temperature or high temperature and high humidity. Has improved.
  • Patent Document 1 and Patent Document 2 have been studied for improvement by controlling the strain accompanying temperature change and the strain accompanying moisture absorption / desorption, a film having a low glass transition temperature such as a polyethylene terephthalate film is used. In this case, the influence of the residual strain (heat shrinkage rate) originally possessed by the film should not be taken into consideration.
  • the problem to be solved by the present invention is to provide a liquid crystal display device capable of highly controlling curling of a laminate comprising a polarizing plate / liquid crystal cell / polarizing plate in the liquid crystal display device.
  • a polarizing plate is usually laminated on one surface of a liquid crystal cell so that the transmission axis direction of the polarizer is parallel to the long side direction of the liquid crystal display device, and the polarizer absorbs on the other surface.
  • Polarizers are stacked so that the axial direction is parallel to the long side of the liquid crystal display device.
  • the problem of the form factor that curls are likely to occur due to the contraction of the polarizing plate having the longer side of the polarizer absorption axis having a large shrinkage force (the curl is In general, it tends to occur in the long side direction), and due to the influence of the asymmetrical configuration of the upper and lower polarizing plates in the liquid crystal panel, the liquid crystal panel has the polarizer transmission axis of the upper and lower polarizing plates arranged in crossed Nicols as the long side
  • the present inventors have found that it is the essence of the problem to be convex toward the polarizing plate.
  • the shrinkage force of a film is measured using a TMA or the like to set the initial length with a minimal load at a low temperature at the start of the test, and measure the force in the shrinking direction during temperature rise while maintaining the initial length. To do.
  • thermal shrinkage due to an increase in the free volume / occupied volume of the polymer due to the temperature increase at the same time as the shrinkage due to the recovery of residual strain accompanying the conformational change of the polymer (hereinafter simply referred to as thermal shrinkage)
  • thermal shrinkage In the temperature range near the glass transition temperature of the polyester film (for example, about Tg + 50 ° C.), the thermal shrinkage is less than the thermal expansion. It expands and no contractile force is observed.
  • the representative present invention is as follows. Item 1.
  • a liquid crystal display device having a liquid crystal cell, a polarizing plate A bonded to one surface of the liquid crystal cell, and a polarizing plate B bonded to the other surface of the liquid crystal cell
  • the polarizing plate A has a structure in which the transmission axis direction of the polarizer is parallel to the long side direction of the liquid crystal display device, and a polyester film is laminated on at least one surface of the polarizer.
  • the polarizing plate B has a structure in which the absorption axis direction of the polarizer is parallel to the long side direction of the liquid crystal display device, and a protective film is laminated on at least one surface of the polarizer.
  • the contraction force F f in the long side direction of the liquid crystal display device of the polyester film and the contraction force F p in the long side direction of the liquid crystal display device of the polarizer included in the polarizing plate B satisfy the following formula (1): Liquid crystal display device.
  • Item 4. Item 4. The liquid crystal display device according to any one of Items 1 to 3, wherein the polyester film has a thickness of 40 to 200 ⁇ m.
  • Item 5. Item 5. The liquid crystal display device according to any one of items 1 to 4, wherein an inclination of an orientation main axis of the polyester film with respect to a long side direction or a short side direction of the liquid crystal display device is 15 degrees or less.
  • the liquid crystal display device according to any one of items 1 to 5, wherein an inclination of the shrink main axis of the polyester film with respect to a long side direction or a short side direction of the liquid crystal display device is 15 degrees or less.
  • Item 7 In a liquid crystal panel having a liquid crystal cell, a polarizing plate A bonded to one surface of the liquid crystal cell, and a polarizing plate B bonded to the other surface of the liquid crystal cell, The polarizing plate A has a structure in which the transmission axis direction of the polarizer is parallel to the long side direction of the polarizing plate A, and a polyester film is laminated on at least one surface of the polarizer.
  • the polarizing plate B has a structure in which the absorption axis direction of the polarizer is parallel to the long side direction of the polarizing plate B, and a protective film is laminated on at least one surface of the polarizer.
  • the liquid crystal panel in which the contraction force F f in the long side direction of the polarizing plate A of the polyester film and the contraction force F p in the long side direction of the polarizing plate B of the polarizer included in the polarizing plate B satisfy the following formula (1).
  • Item 10. Item 10. The liquid crystal panel according to any one of items 7 to 9, wherein the polyester film has a thickness of 40 to 200 ⁇ m.
  • Item 11. Item 11. The liquid crystal panel according to any one of items 7 to 10, wherein an inclination of an orientation main axis of the polyester film with respect to a long side direction or a short side direction of the liquid crystal panel is 15 degrees or less.
  • liquid crystal display device in which curling of a laminate (liquid crystal panel) composed of a polarizing plate / liquid crystal cell / polarizing plate generated in a high temperature or high temperature and high humidity environment is reduced.
  • the screen of the liquid crystal display device is usually rectangular and has a long side and a short side.
  • the “long side direction of the liquid crystal display device” is a direction parallel to the long side of the liquid crystal display device, and includes “long side direction of the polarizing plate A”, “long side direction of the polarizing plate B”, This is the same as “the long side direction of the polarizer of the polarizing plate B” and “the long side direction of the polyester film of the polarizing plate A”. Therefore, in this specification, “the long side direction of the liquid crystal display device” means “the long side direction of the polarizing plate A”, “the long side direction of the polarizing plate B”, and “the long side of the polarizer included in the polarizing plate B”.
  • the “short-side direction of the liquid crystal display device” means a direction parallel to the short side of the liquid crystal display device and a direction perpendicular to the long-side direction.
  • the liquid crystal display device of the present invention has at least a liquid crystal cell, a polarizing plate A bonded to one surface of the liquid crystal cell, and a polarizing plate B bonded to the other surface of the liquid crystal cell.
  • a liquid crystal cell and a polarizing plate can usually be bonded together through an adhesion layer.
  • the liquid crystal display device can include constituent members that are usually used in the liquid crystal display device, such as a backlight.
  • the liquid crystal cell has a structure in which liquid crystal is sandwiched between two glass substrates.
  • the thickness of the glass substrate constituting the liquid crystal cell may be 0.7 mm or less, 0.6 mm or less, 0.5 mm or less, 0.4 mm or less, 0.3 mm or less, or 0.25 mm or less. preferable.
  • the transmission axis direction of the polarizer is parallel to the long side direction of the liquid crystal display device (that is, the transmission axis direction of the polarizer is parallel to the long side direction of the polarizing plate A). It has a structure in which a polyester film (used as a polarizer protective film) is laminated on at least one surface of the child.
  • a protective film having a low retardation such as a TAC film, a cyclic olefin film, an acrylic film, or an optical compensation film can be laminated on the surface of the polarizer opposite to the surface on which the polyester film is laminated.
  • the protective film having a low retardation can be, for example, a protective film having a retardation of 500 nm or less, 400 nm or less, 300 nm or less, 200 nm or less, 100 nm or less, or 50 nm or less.
  • the polarizing plate A has a structure in which a polyester film is laminated only on one side of the polarizer and a protective film or an optical compensation film is not laminated on the other side of the polarizer.
  • the polyester film can be placed on the liquid crystal cell side of the polarizer, or on the distal side (outside) of the liquid crystal cell (or both sides), but on the distal side (outside) of the polarizer liquid crystal cell It is preferable to arrange.
  • the transmission axis direction of the polarizer is parallel to the long side direction of the liquid crystal display device, but it is most preferable that the transmission axis direction be completely parallel, but this is a concept that allows a slight deviation. That is, the angle formed by the transmission axis direction of the polarizer and the long side direction of the liquid crystal display device is preferably 7 degrees or less, preferably 5 degrees or less, preferably 3 degrees or less, preferably 2 degrees or less, and 1 degree or less. Is preferred, most preferably 0 degrees.
  • the absorption axis direction of the polarizer is parallel to the long-side direction of the liquid crystal display device (that is, the absorption axis of the polarizer is parallel to the long-side direction of the polarizing plate B). It is the structure where the protective film was laminated
  • a protective film with low retardation such as a TAC film, a cyclic olefin film, an acrylic film, or an optical compensation film can be laminated on the protective film.
  • the protective film having a low retardation can be, for example, a protective film having a retardation of 500 nm or less, 400 nm or less, 300 nm or less, 200 nm or less, 100 nm or less, or 50 nm or less.
  • a polyester film can also be laminated
  • the polarizing plate B may have a structure in which a polyester film is laminated on one surface of a polarizer and the above-described protective film or optical compensation film is laminated on the other surface.
  • the polarizing plate B is also a preferable embodiment in which a polyester film is laminated on only one side of the polarizer and a protective film or an optical compensation film is not laminated on the other side of the polarizer.
  • the absorption axis direction of the polarizer be parallel to the long side direction of the liquid crystal display device, but it is most preferably completely parallel, but a slight deviation is allowed. That is, the angle formed between the absorption axis direction of the polarizer and the long side direction of the liquid crystal display device is preferably 7 degrees or less, preferably 5 degrees or less, preferably 3 degrees or less, preferably 2 degrees or less, and 1 degree or less. Is preferred, most preferably 0 degrees.
  • the polarizing plate A may be used as either a polarizing plate on the viewing side or a polarizing plate on the backlight side from the liquid crystal cell, but is generally preferably disposed as a polarizing plate on the backlight side.
  • the polarizing plate B may be used as either a polarizing plate on the viewing side or a polarizing plate on the backlight side of the liquid crystal cell, but is generally preferably disposed as a polarizing plate on the viewing side. That is, a liquid crystal display device having a backlight source, a polarizing plate A, a liquid crystal cell, and a polarizing plate B in this order is preferable.
  • the liquid crystal display device may include other members between them.
  • F f / F p 0.1 ⁇ F f / F p ⁇ 2.
  • the lower limit value of F f / F p is preferably 0.2 or 0.3.
  • the upper limit value of F f / F p is 1.9, 1.8, 1.7, 1.6, 1.5, 1.4, 1.3, 1.2, 1.1, 1.0, It is preferably 0.9, 0.8 or 0.7.
  • F f indicates the shrinkage force in the long side direction of the liquid crystal display device of the polyester film of the polarizing plate A, and the thickness of the polyester film (mm) ⁇ elastic modulus (N / mm 2 ) ⁇ heat shrinkage rate (%) ⁇ 100. It is defined by x1000.
  • F p indicates the contraction force of the polarizer of the polarizing plate B in the long side direction of the liquid crystal display device, and the thickness (mm) ⁇ elastic modulus (N / mm 2 ) ⁇ thermal contraction rate (%) of the polarizer of the polarizing plate B.
  • ⁇ 100 ⁇ 1000 is defined.
  • the elastic modulus and the thermal contraction rate are both values in the long side direction of the liquid crystal display device.
  • the contraction force of the polarizing plate B is mainly expressed by the polarizer, and the contraction force changes depending on the thickness of the polarizer and the film forming conditions. Therefore, it is desirable to adjust the shrinkage force of the polyester film used for the polarizing plate A accordingly.
  • the polyester film used for the polarizing plate A preferably has an elastic modulus in the long side direction of the liquid crystal display device of 1000 to 9000 N / mm 2 .
  • the shrinkage force of the polyester film can be controlled by the elastic modulus, in order to increase the elastic modulus in the long side direction of the liquid crystal display device, it is highly oriented in the long side direction of the liquid crystal display device and the crystallinity is increased. Need to be high. Therefore, when the longitudinal direction of the elastic modulus is more than 9000 N / mm 2, since the problem of easily tearing becomes apparent, the upper limit is preferably 9000 N / mm 2, more preferably 8000 N / mm 2, More preferably, it is 7000 N / mm 2 .
  • the lower limit of the elastic modulus is preferably 1000 N / mm 2, more preferably 1500 N / mm 2, further preferably 1800 N / mm 2.
  • the elastic modulus can be measured by the method employed in the examples described later.
  • the polyester film used for the polarizing plate A preferably has a thermal shrinkage of 0.1 to 5% in the long side direction of the liquid crystal display device at 30 ° C. for 30 minutes.
  • the lower limit of the heat shrinkage rate is preferably 0.3% or more, preferably 0.4% or more, preferably 0.5% or more, and preferably 0.7% or more.
  • the upper limit of the heat shrinkage rate is preferably 4% or less, preferably 3% or less, and preferably 2% or less. When the heat shrinkage rate is lower than 0.1%, that is, in the range of 0.01 to 0.099%, it is difficult to control the heat shrinkage rate without variation.
  • thermal shrinkage rate can be measured by the method employed in the examples described later.
  • the polyester film used for the polarizing plate A preferably has a thickness of 40 to 200 ⁇ m.
  • the thickness of the polyester film is less than 40 ⁇ m, the polyester film is easily broken, and flatness is likely to be poor due to insufficient rigidity.
  • the lower limit is substantially 40 ⁇ m.
  • the film thickness exceeds 200 ⁇ m, the variation in the elastic modulus or heat shrinkage in the long side direction increases accordingly, which makes it difficult to control and increases the cost.
  • the thickness of the polyester film can be measured by the method employed in the examples described later.
  • the polyester film used for the polarizing plate A desirably has an inclination of 15 degrees or less between the orientation principal axis of the polyester film and the long side direction or the short side direction of the liquid crystal display device.
  • the stretched polyester film usually has anisotropy of elastic modulus in the film plane, but the anisotropy of the elastic modulus and optical anisotropy of the stretched polyester film generally coincide. Therefore, with respect to the alignment main axis determined from the optical anisotropy, the narrow angle with the long side direction or the short side direction of the liquid crystal display device is set to 15 degrees or less so that the direction with the higher elastic modulus is the long side of the liquid crystal display device.
  • the orientation main axis of the polyester film can be measured according to the measurement method employed in Examples described later.
  • the polyester film used for the polarizing plate A preferably has a narrow angle of 15 degrees or less with respect to the major axis of the liquid crystal display device or the short side direction with respect to the shrink main axis of the polyester film.
  • the stretched polyester film usually has anisotropy in heat shrinkage within the film plane, and the shrinkage main axis has an inclination.
  • the narrow angle between the contraction main axis and the long side direction or the short side direction is larger than 15 degrees, the tendency of curling in the oblique direction becomes remarkable, which is not preferable.
  • the narrow angle between the shrink main axis of the polyester film used for the polarizing plate A and the long side direction or the short side direction of the liquid crystal display device is preferably 15 degrees or less, more preferably 10 degrees or less, 9 degrees or less, or 8 degrees or less. preferable.
  • the contraction main axis can be measured according to the measurement method employed in Examples described later.
  • the polyester film used for the polarizing plate A preferably has in-plane retardation within a specific range from the viewpoint of suppressing rainbow spots observed on the screen of the liquid crystal display device.
  • the lower limit of the in-plane retardation is preferably 3000 nm or more, 5000 nm or more, 6000 nm or more, 7000 nm or more, or 8000 nm or more.
  • the upper limit of the in-plane retardation is preferably 30000 nm or less, more preferably 18000 nm or less, and further preferably 15000 nm or less.
  • the polyester film when using a polyester film as a protective film also for the polarizing plate B, it is preferable that the polyester film also has in-plane retardation of the said range.
  • the retardation of the polyester film can be obtained by measuring the biaxial refractive index and thickness, or can be obtained by using a commercially available automatic birefringence measuring device such as KOBRA-21ADH (Oji Scientific Instruments).
  • the refractive index can be obtained by an Abbe refractometer (measurement wavelength: 589 nm).
  • the ratio of the in-plane retardation (Re) to the retardation in the thickness direction (Rth) (Re / Rth) of the polyester film used for the polarizing plate A is preferably 0.2 or more, preferably 0.3 or more, preferably Is 0.4 or more, preferably 0.5 or more, more preferably 0.5 or more, and still more preferably 0.6 or more.
  • the ratio of the in-plane retardation to the thickness direction retardation (Re / Rth) is larger, the birefringence effect is more isotropic, and the occurrence of rainbow-like color spots due to the observation angle tends to be less likely to occur.
  • the ratio of the retardation to the retardation in the thickness direction (Re / Rth) is 2.0. Therefore, the ratio of the retardation to the retardation in the thickness direction (Re / Rth)
  • the upper limit is preferably 2.0.
  • a preferable upper limit of Re / Rth is 1.2 or less.
  • the thickness direction retardation means an average of retardation obtained by multiplying two birefringences ⁇ Nxz and ⁇ Nyz by the film thickness d when the film is viewed from the cross section in the thickness direction.
  • the ratio (Re / Rth) of the in-plane retardation (Re) and the retardation in the thickness direction (Rth) is also in the above range. It is preferable.
  • the polyester film used for the polarizing plate A preferably has a NZ coefficient of 2.5 or less, more preferably 2.0 or less, and even more preferably 1 from the viewpoint of suppressing iridescent color spots. .8 or less, more preferably 1.6 or less. And since a NZ coefficient will be 1.0 in a perfect uniaxial (uniaxial symmetry) film, the minimum of a NZ coefficient is 1.0. However, it should be noted that the mechanical strength in the direction perpendicular to the orientation direction tends to decrease significantly as the film approaches a perfect uniaxial (uniaxial symmetry) film. In addition, when using a polyester film as a protective film also for the polarizing plate B, it is preferable that the polyester film also has a NZ coefficient in the said range.
  • the NZ coefficient is represented by
  • the orientation axis of the film is obtained using a molecular orientation meter (MOA-6004 type molecular orientation meter, manufactured by Oji Scientific Instruments Co., Ltd.), and the biaxial refractive index (Ny, Nx, where the orientation axis direction and the direction perpendicular thereto are perpendicular) Ny> Nx) and the refractive index (Nz) in the thickness direction are determined by Abbe's refractometer (manufactured by Atago Co., Ltd., NAR-4T, measurement wavelength 589 nm). The value obtained in this manner can be substituted for
  • the value of Ny-Nx of the polyester film is preferably 0.05 or more, more preferably 0.07 or more, from the viewpoint of suppressing iridescent color spots. Preferably it is 0.08 or more, More preferably, it is 0.09 or more, Most preferably, it is 0.1 or more.
  • the upper limit is not particularly defined, but in the case of a polyethylene terephthalate film, the upper limit is preferably about 1.5.
  • the polyester film preferably has a Ny-Nx value within the above range.
  • the polyester film used for the polarizing plate A can be obtained from any polyester resin.
  • the type of the polyester resin is not particularly limited, and any polyester resin obtained by condensing dicarboxylic acid and diol can be used.
  • the polyester film is also the same.
  • dicarboxylic acid component examples include terephthalic acid, isophthalic acid, orthophthalic acid, 2,5-naphthalenedicarboxylic acid, 2,6-naphthalenedicarboxylic acid, 1,4-naphthalenedicarboxylic acid, , 5-Naphthalenedicarboxylic acid, diphenylcarboxylic acid, diphenoxyethanedicarboxylic acid, diphenylsulfonecarboxylic acid, anthracene dicarboxylic acid, 1,3-cyclopentanedicarboxylic acid, 1,3-cyclohexanedicarboxylic acid, 1,4-cyclohexanedicarboxylic acid , Hexahydroterephthalic acid, hexahydroisophthalic acid, malonic acid, dimethylmalonic acid, succinic acid, 3,3-diethylsuccinic acid, glutaric acid, 2,2-dimethylglu
  • diol component examples include ethylene glycol, propylene glycol, hexamethylene glycol, neopentyl glycol, 1,2-cyclohexanedimethanol, 1,4-cyclohexanedimethanol, decamethylene glycol, 1 , 3-propanediol, 1,4-butanediol, 1,5-pentanediol, 1,6-hexadiol, 2,2-bis (4-hydroxyphenyl) propane, bis (4-hydroxyphenyl) sulfone, etc. Can be mentioned.
  • the dicarboxylic acid component and the diol component constituting the polyester resin can be used alone or in combination of two or more.
  • Suitable polyester resins constituting the polyester film include, for example, polyethylene terephthalate, polypropylene terephthalate, polybutylene terephthalate, polyethylene naphthalate, and more preferably polyethylene terephthalate and polyethylene naphthalate.
  • other copolymer components may be included.
  • These resins are excellent in transparency and excellent in thermal and mechanical properties.
  • polyethylene terephthalate is a suitable material because it can achieve a high elastic modulus and the heat shrinkage rate is relatively easy to control.
  • the polarizing plate A used in the liquid crystal display device of the present invention is desirably integrated with the glass plate of the liquid crystal cell in a state in which the thermal shrinkage rate of the polyester film remains, an easy adhesion layer, a hard coat layer,
  • the drying temperature can be set low, UV irradiation, This is an embodiment that is preferably performed by a method having a small thermal history such as electron beam irradiation.
  • applying these functional layers during the process of forming the polyester film is more effective. This is a desirable embodiment.
  • the polyester film used by this invention can be manufactured in accordance with the manufacturing method of a general polyester film.
  • the polyester resin is melted and the non-oriented polyester extruded and formed into a sheet shape is stretched in the longitudinal direction by utilizing the speed difference of the roll at a temperature equal to or higher than the glass transition temperature, and then stretched in the transverse direction by a tenter.
  • the method of performing heat processing is mentioned.
  • a uniaxially stretched film or a biaxially stretched film may be used.
  • MD is an abbreviation for Machine Direction, and may be referred to as a film flow direction, a longitudinal direction, and a longitudinal direction in this specification.
  • TD is an abbreviation for Transverse Direction, and may be referred to as a width direction and a horizontal direction in this specification.
  • the polyester film used as the polarizer protective film for the polarizing plate A adjusts the shrinkage force F f so that 0.1F p ⁇ F f ⁇ 2F p .
  • the elastic modulus of the polyester film used as the polarizer protective film for the polarizing plate A is MD when the polarizer transmission axis direction (that is, the long side direction of the liquid crystal display device) coincides with the MD when the polyester film is formed.
  • the elastic modulus of the polyester film coincides with the TD at the time of forming the polyester film
  • the elastic modulus of the TD may be adjusted by a conventionally known method of the stretched polyester film. Specifically, when the direction is the stretching direction, the stretching ratio may be set high, and when the direction is the direction orthogonal to the stretching direction, the stretching ratio may be set low.
  • the thermal shrinkage rate of the polyester film used as the polarizer protective film for the polarizing plate A is when the transmission axis direction of the polarizer (that is, the long side direction of the liquid crystal display device) matches the MD at the time of forming the polyester film. If the thermal shrinkage rate of MD coincides with the TD at the time of forming the polyester film, the thermal shrinkage rate of TD may be adjusted by a conventionally known method of stretched polyester film.
  • the distance between the clip holding the film width direction end and the adjacent clip is expanded to the MD. It can be adjusted by shrinking to MD by reducing the clip interval or the clip interval.
  • the film is stretched or shrunk to MD by adjusting the film pulling force. It is possible to adjust by.
  • the thermal shrinkage rate changes during the heating and cooling process, so the film pulling force is adjusted to stretch or shrink the MD. It is also possible to make adjustments.
  • the gap between the clip holding the film width direction end and the clip located on the opposite side of the width direction is expanded.
  • it can be adjusted by stretching to TD or by shrinking to TD by reducing.
  • MD or TD it is desirable to adjust the heat shrinkage rate within the target temperature range of the present invention.
  • the inclination of the shrink main axis of the polyester film used as the polarizer protective film for the polarizing plate A is a cooling process after stretching and heat treatment by the polyester film tenter.
  • it can be adjusted in an off-line process after film formation. Specifically, thermal stress due to shrinkage due to stretching and cooling that could not be completely removed by heat fixation in the cooling process has occurred, and depending on the balance between the two in the film flow direction, it is drawn in upstream or downstream. Retraction occurs, causing a phenomenon that the contraction main axis is tilted.
  • the shrinkage force in the film flow direction in the cooling step (the sum of the shrinkage force accompanying stretching and the shrinkage force accompanying cooling) to be uniform.
  • a conventionally known method may be used as a method for shrinking or stretching.
  • care should be taken because the film shrinks freely in the width direction below the cut / separated temperature range and the thermal shrinkage rate below the temperature range becomes small.
  • Shrinkage force The shrinkage force of the polarizer and the polyester film was calculated from the following equation.
  • the film thickness, elastic modulus, and heat shrinkage rate are measured values described below.
  • Contraction force (N / m) Film thickness (mm) ⁇ elastic modulus (N / mm 2 ) ⁇ heat shrinkage rate (%) ⁇ 100 ⁇ 1000
  • the elastic modulus of the polarizer and the polyester film is a dynamic viscoelasticity measuring device manufactured by Seiko Instruments Inc. (DMS6100) according to JIS-K7244 (DMS) after standing for 168 hours in an environment of 25 ° C. and 50 RH%. Evaluation was carried out using. Measure the temperature dependence from 25 ° C to 120 ° C under the conditions of tension mode, drive frequency of 1 Hz, distance between chucks of 5 mm, and heating rate of 2 ° C / min, and calculate the average storage elastic modulus of 30 ° C to 100 ° C. Elastic modulus was used. The elastic modulus in the direction parallel to the long side direction of the liquid crystal display device was measured.
  • the heat shrinkage rate in the present invention is defined as a value in a direction parallel to the long side direction of the liquid crystal display device among heat shrinkage rates calculated by the following calculation formula.
  • Thermal shrinkage (length before treatment ⁇ length after treatment) / length before treatment ⁇ 100
  • the inclination of the contraction main axis is an angle at which the thermal contraction rate measured every 1 ° is maximized, and is defined by a narrow angle from the long side direction or the short side direction. That is, the inclination of the contraction main axis is in the range of 0 to 45 °.
  • orientation of the orientation axis of the polyester film is measured by measuring the orientation main axis using a molecular orientation meter (MOA-6004 type molecular orientation meter, manufactured by Oji Scientific Instruments Co., Ltd.). It was defined by a narrow angle from the direction. In other words, the inclination of the alignment main axis is in the range of 0 to 45 °.
  • MOA-6004 type molecular orientation meter manufactured by Oji Scientific Instruments Co., Ltd.
  • the maximum curl height was set to 5 mm or less as a favorable range. Although curl is a phenomenon that should be expressed by curvature, it is evaluated by height for simplicity. In addition, the curl phenomenon becomes bowl-shaped when the sample size increases with respect to the rigidity of the sample, and the phenomenon that the curvature does not become constant in the film may occur, but all the results of this example are constant. Have confirmed.
  • the biaxial refractive index (the refractive index in the slow axis direction: Ny, the fast axis (the refractive index in the direction perpendicular to the slow axis direction): Nx), and the refractive index in the thickness direction ( Nz) was determined by an Abbe refractometer (manufactured by Atago Co., Ltd., NAR-4T, measurement wavelength 589 nm). NZ coefficient was calculated
  • the biaxial refractive index anisotropy ( ⁇ Nxy) was determined by the following method. Using a molecular orientation meter (MOA-6004 type molecular orientation meter, manufactured by Oji Scientific Instruments Co., Ltd.), determine the slow axis direction of the film, 4 cm so that the slow axis direction is parallel to the long side of the measurement sample.
  • MOA-6004 type molecular orientation meter manufactured by Oji Scientific Instruments Co., Ltd.
  • a rectangle of ⁇ 2 cm was cut out and used as a measurement sample.
  • Abbe refracts the biaxial refractive index (the refractive index in the slow axis direction: Ny, the refractive index in the direction perpendicular to the slow axis direction: Nx), and the refractive index (Nz) in the thickness direction.
  • ) of the biaxial refractive index difference was determined as a refractive index anisotropy ( ⁇ Nxy), which was obtained by a refractive index meter (NAGO-4T manufactured by Atago Co., Ltd., measurement wavelength 589 nm).
  • the thickness d (nm) of the film was measured using an electric micrometer (manufactured by Fine Reef, Millitron 1245D), and the unit was converted to nm.
  • Retardation (Re) was determined from the product ( ⁇ Nxy ⁇ d) of refractive index anisotropy ( ⁇ Nxy) and film thickness d (nm).
  • ) and ⁇ Nyz (
  • the obtained polyethylene terephthalate resin (A) had an intrinsic viscosity of 0.62 dl / g and contained substantially no inert particles and internally precipitated particles. (Hereafter, abbreviated as PET (A).)
  • PET (B) 10 parts by weight of a dried UV absorber (2,2 ′-(1,4-phenylene) bis (4H-3,1-benzoxazinon-4-one), PET (A) containing no particles (inherent viscosity Was 0.62 dl / g) and 90 parts by mass were mixed, and a polyethylene terephthalate resin (B) containing an ultraviolet absorber was obtained using a kneading extruder (hereinafter abbreviated as PET (B)).
  • a transesterification reaction and a polycondensation reaction were carried out by a conventional method, and as a dicarboxylic acid component (based on the whole dicarboxylic acid component) 46 mol% terephthalic acid, 46 mol% isophthalic acid and 8 mol% sodium 5-sulfonatoisophthalate, A water-dispersible sulfonic acid metal group-containing copolymer polyester resin having a composition of 50 mol% ethylene glycol and 50 mol% neopentyl glycol (relative to the entire glycol component) was prepared as a glycol component.
  • Example 1 After drying 90 parts by mass of PET (A) resin pellets containing no particles as a raw material for the base film intermediate layer and 10 parts by mass of PET (B) resin pellets containing an ultraviolet absorber at 135 ° C. for 6 hours under reduced pressure (1 Torr) , And supplied to the extruder 2 (for the intermediate layer II layer). Also, the PET (A) was dried by a conventional method and supplied to the extruder 1 (for the outer layer I layer and the outer layer III) and dissolved at 285 ° C. .
  • the unstretched film on which this coating layer was formed was guided to a tenter stretching machine, guided to a hot air zone at a temperature of 105 ° C. while being gripped by a clip, and stretched 4.0 times to TD.
  • heat treatment was performed at a temperature of 180 ° C. for 30 seconds, and then the film cooled to 100 ° C. was stretched by 1% in MD, and then the clips holding both ends of the film cooled to 60 ° C. were opened.
  • a jumbo roll made of a uniaxially oriented PET film having a film thickness of about 80 ⁇ m, and the resulting jumbo roll is equally divided into three slit rolls (L (left side), C ( Center), R (right side)).
  • the polarizer protective film 1 was obtained from the slit roll located in R (the central part of the slit roll located in R was used as the polarizer protective film 1).
  • a polarizer protective film 1 is attached to one side of a polarizer made of PVA, iodine and boric acid (the contraction force in the absorption axis direction of the polarizer is 5100 N / m) so that the transmission axis of the polarizer and the MD of the film are parallel to each other. I attached. Further, a TAC film (manufactured by Fuji Film Co., Ltd., thickness 80 ⁇ m) was attached to the opposite surface of the polarizer. In this manner, a polarizing plate (polarizing plate A) whose long side direction matches the transmission axis direction of the polarizer and a polarizing plate (polarizing plate B) whose long side direction matches the absorption axis direction of the polarizer were prepared.
  • a liquid crystal panel was prepared by bonding through PSA so as to be on the opposite side.
  • a liquid crystal display device was produced by incorporating this liquid crystal panel into a housing.
  • Example 2 In the production of the polarizer protective film 1 of Example 1, a polarizer protective film 2 was obtained in the same manner as the polarizer protective film 1 except that the film cooled to 100 ° C. was stretched 2.5% in the longitudinal direction. .
  • a liquid crystal display device was prepared in the same manner as in Example 1 except that the polarizer protective film 1 was replaced with the polarizer protective film 2 in Example 1.
  • Example 3 In the production of the polarizer protective film 1 of Example 1, a polarizer protective film 3 was obtained in the same manner as the polarizer protective film 1 except that the film cooled to 100 ° C. was stretched 4% in the longitudinal direction. In Example 1, the contraction force in the absorption axis direction was changed from a polarizer of 5100 N / m to a polarizer of 11200 N / m, except that the polarizer protective film 1 was replaced by the polarizer protective film 3 Example 1 In the same manner, a liquid crystal display device was produced.
  • Example 4 Other than using a blend of 90% by mass of PET (A) and 10% by mass of PBT as a raw material for the I layer, the II layer, and the III layer, and that the film cooled to 100 ° C. was stretched by 4% in the longitudinal direction.
  • the contraction force in the absorption axis direction was changed from a polarizer of 5100 N / m to a polarizer of 11200 N / m, and Example 1 was changed except that the polarizer protective film 1 was replaced by the polarizer protective film 4.
  • the PBT used was NV5020 (0.52 dl / g) manufactured by Mitsubishi Engineering Plastics.
  • Example 5 A polarizer protective film 5 was obtained in the same manner as the polarizer protective film 1 except that the film thickness after stretching was adjusted to 50 ⁇ m by adjusting the rotation speed of the casting roll.
  • a liquid crystal display device was prepared in the same manner as in Example 1 except that the polarizer protective film 1 was replaced with the polarizer protective film 5 in Example 1.
  • Example 6 A polarizer protective film 6 was obtained in the same manner as the polarizer protective film 5 except that the film cooled to 100 ° C. was stretched 2.5% in the longitudinal direction.
  • a liquid crystal display device was produced in the same manner as in Example 1 except that the polarizer protective film 1 was replaced with the polarizer protective film 6 in Example 1.
  • Example 7 A polarizer protective film 7 was obtained in the same manner as the polarizer protective film 5 except that the film cooled to 100 ° C. was stretched 4% in the longitudinal direction.
  • the contraction force in the absorption axis direction was changed from a polarizer of 5100 N / m to a polarizer of 11200 N / m, and Example 1 except that the polarizer protective film 1 was replaced with the polarizer protective film 7.
  • a liquid crystal display device was produced.
  • Example 8 A polarizer protective film 8 was obtained in the same manner as the polarizer protective film 1 except that the film thickness after stretching was 160 ⁇ m by adjusting the rotational speed of the casting roll.
  • a liquid crystal display device was produced in the same manner as in Example 1 except that the polarizer protective film 1 was replaced with the polarizer protective film 8 in Example 1.
  • Example 9 A polarizer protective film 9 was obtained in the same manner as the polarizer protective film 8 except that the film cooled to 100 ° C. was stretched 2.5% in the width direction. Next, the polarizer having a contraction force in the absorption axis direction was changed from a polarizer of 5100 N / m to a polarizer of 11200 N / m, and the polarizing axis was bonded so that the transmission axis of the polarizer and the TD of the polarizer protective film were parallel.
  • a liquid crystal display device was obtained in the same manner as in Example 1 except that the plate A and the polarizing plate B were prepared and that the polarizer protective film 1 was replaced with the polarizer protective film 9.
  • Example 10 A polarizer protective film 10 was obtained in the same manner as the polarizer protective film 1 except that the film was stretched 4.0 times in MD and 1.0 times in TD.
  • a liquid crystal display device was produced in the same manner as in Example 1 except that the polarizer protective film 1 was replaced with the polarizer protective film 10 in Example 1.
  • Example 11 A polarizer protective film 11 was obtained in the same manner as the polarizer protective film 10 except that the film cooled to 100 ° C. was stretched 1.5% in MD.
  • a liquid crystal display device was produced in the same manner as in Example 1 except that the polarizer protective film 1 was replaced with the polarizer protective film 11 in Example 1.
  • Example 12 A polarizer protective film 12 was obtained in the same manner as the polarizer protective film 10 except that the film cooled to 100 ° C. was stretched by 2.5% in MD. The same as Example 1 except that the polarizer having a contraction force in the absorption axis direction was changed from a polarizer of 5100 N / m to a polarizer of 11200 N / m, and the polarizer protective film 1 was changed to the polarizer protective film 12. Thus, a liquid crystal display device was obtained.
  • Example 13 Except for using a blend of 90% by mass of PET (A) and 10% by mass of PBT as a raw material for the I layer, the II layer, and the III layer, and making the film cooled to 100 ° C. into 3% stretched in MD.
  • a polarizer protective film 13 was obtained in the same manner as the polarizer protective film 10.
  • the PBT used was NV5020 (0.52 dl / g) manufactured by Mitsubishi Engineering Plastics.
  • Example 14 Polarizer in the same manner as the polarizer protective film 10 except that the film thickness after stretching was adjusted to 50 ⁇ m by adjusting the rotation speed of the casting roll, and the film cooled to 100 ° C. was stretched 1.5% to MD. A protective film 14 was obtained. A liquid crystal display device was obtained in the same manner as in Example 1 except that the polarizer protective film 1 was replaced with the polarizer protective film 14.
  • Example 15 A polarizer protective film 15 was obtained in the same manner as the polarizer protective film 14 except that the film cooled to 100 ° C. was stretched by 2% in MD.
  • a liquid crystal display device was obtained in the same manner as in Example 1 except that the polarizer protective film 1 was replaced with the polarizer protective film 15.
  • Example 16 A polarizer protective film 16 was obtained in the same manner as the polarizer protective film 14 except that the film cooled to 100 ° C. was stretched 5% in TD. Next, the polarizing plate A and the polarizing plate B were prepared by bonding so that the transmission axis of the polarizer and the TD direction of the polarizer protective film were parallel, and the polarizer protective film 1 was attached to the polarizer protective film 16. A liquid crystal display device was obtained in the same manner as in Example 1 except that it was replaced with.
  • Example 17 A polarizer protective film 20 was obtained in the same manner as the polarizer protective film 10 except that the film cooled to 100 ° C. was stretched by 2% in MD.
  • a liquid crystal display device was produced in the same manner as in Example 1 except that the polarizer protective film 1 was replaced with the polarizer protective film 20 in Example 1.
  • Example 18 A polarizer protective film 21 was obtained in the same manner as the polarizer protective film 10 except that the film cooled to 100 ° C. was stretched to 2.5% in MD.
  • a liquid crystal display device was produced in the same manner as in Example 1 except that the polarizer protective film 1 was replaced with the polarizer protective film 21 in Example 1.
  • a polarizer protective film 17 was obtained in the same manner as the polarizer protective film 1 except that the clips holding both ends of the film were opened at 95 ° C. in the cooling step after stretching and heat setting. Except that the polarizer protective film 1 was replaced with the polarizer protective film 17, and the polarizing plate A and the polarizing plate B were prepared by bonding so that the transmission axis of the polarizer and the TD of the polarizer protective film were parallel to each other.
  • a liquid crystal display device was obtained in the same manner as in Example 1.
  • a polarizer protective film 18 was obtained in the same manner as the polarizer protective film 14 except that the film cooled to 100 ° C. was stretched 0.8% in the width direction.
  • the polarizer having a contraction force in the absorption axis direction was changed from a polarizer of 5100 N / m to a polarizer of 11200 N / m, and the polarizer protective film 1 was changed to the polarizer protective film 18, and the transmission axis and polarization of the polarizer
  • a liquid crystal display device was obtained in the same manner as in Example 1 except that the polarizing plate A and the polarizing plate B were prepared by bonding so that the TD of the child protective film was parallel.
  • a polarizer protective film 19 was obtained in the same manner as the polarizer protective film 8 except that the film cooled to 100 ° C. was stretched 0.3% in the width direction.
  • the polarizer having a contraction force in the absorption axis direction was changed from a polarizer of 5100 N / m to a polarizer of 11200 N / m, and the polarizer protective film 1 was changed to the polarizer protective film 19, and the transmission axis and polarization of the polarizer
  • a liquid crystal display device was obtained in the same manner as in Example 1 except that the polarizing plate A and the polarizing plate B were prepared by bonding so that the TD of the child protective film was parallel.
  • liquid crystal panels of the liquid crystal display devices of Examples 1 to 18 and the liquid crystal panels of the liquid crystal display devices of Comparative Examples 1 to 3 were heat-treated for 30 minutes using a gear oven set at 100 ° C.
  • the liquid crystal panel was observed after cooling for 10 minutes in an environment set at 50 ° C. and 50 RH%, no curl was observed in Examples 1 to 16, but curl was observed in Comparative Examples 1 to 3. .
  • Table 1 shows the measurement results of each example.

Landscapes

  • Physics & Mathematics (AREA)
  • Nonlinear Science (AREA)
  • General Physics & Mathematics (AREA)
  • Optics & Photonics (AREA)
  • Mathematical Physics (AREA)
  • Chemical & Material Sciences (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Polarising Elements (AREA)
  • Liquid Crystal (AREA)
PCT/JP2017/011981 2016-03-31 2017-03-24 液晶表示装置 WO2017170216A1 (ja)

Priority Applications (6)

Application Number Priority Date Filing Date Title
CN202010291214.4A CN111443417B (zh) 2016-03-31 2017-03-24 液晶显示装置
CN201780021586.1A CN109073929B (zh) 2016-03-31 2017-03-24 液晶显示装置
KR1020207010384A KR102311948B1 (ko) 2016-03-31 2017-03-24 액정 표시 장치
KR1020187030586A KR102312023B1 (ko) 2016-03-31 2017-03-24 액정 표시 장치
JP2017531407A JP6205089B1 (ja) 2016-03-31 2017-03-24 液晶表示装置
KR1020217032059A KR102502207B1 (ko) 2016-03-31 2017-03-24 편광자 보호 필름, 편광판 및 액정 표시 장치

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2016071202 2016-03-31
JP2016-071202 2016-03-31

Publications (1)

Publication Number Publication Date
WO2017170216A1 true WO2017170216A1 (ja) 2017-10-05

Family

ID=59965538

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2017/011981 WO2017170216A1 (ja) 2016-03-31 2017-03-24 液晶表示装置

Country Status (5)

Country Link
JP (3) JP6205089B1 (ko)
KR (3) KR102312023B1 (ko)
CN (2) CN109073929B (ko)
TW (1) TWI729104B (ko)
WO (1) WO2017170216A1 (ko)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20200034521A (ko) * 2018-09-21 2020-03-31 주식회사 엘지화학 액정 표시 장치
JP2020091494A (ja) * 2017-09-15 2020-06-11 東洋紡株式会社 偏光子保護フィルム、偏光板及び液晶表示装置
CN111712742A (zh) * 2018-06-29 2020-09-25 株式会社Lg化学 偏光板、液晶面板和显示装置
JP2021513116A (ja) * 2018-06-29 2021-05-20 エルジー・ケム・リミテッド 偏光板、液晶パネルおよびディスプレイ装置
US20210356640A1 (en) * 2019-01-11 2021-11-18 Lg Chem, Ltd. Polarizing plate

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2020526797A (ja) * 2017-07-25 2020-08-31 エルジー・ケム・リミテッド 偏光板およびこれを含む液晶表示素子
JP6866339B2 (ja) * 2018-04-11 2021-04-28 住友化学株式会社 偏光板および表示装置
CN110361805B (zh) * 2018-04-11 2022-11-18 住友化学株式会社 偏振板及显示装置
KR102662107B1 (ko) * 2019-01-11 2024-05-02 산진 옵토일렉트로닉스 (난징) 컴퍼니 리미티드 편광판의 제조 방법
KR102621169B1 (ko) * 2019-01-11 2024-01-05 산진 옵토일렉트로닉스 (난징) 컴퍼니 리미티드 편광판의 제조 방법
CN112164324B (zh) * 2020-09-04 2022-07-15 中国科学技术大学 具有改变出射光偏振状态的有机发光显示装置

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010032718A (ja) * 2008-07-28 2010-02-12 Nitto Denko Corp 液晶パネル及び液晶表示装置
WO2013187134A1 (ja) * 2012-06-11 2013-12-19 富士フイルム株式会社 液晶表示装置
JP2014219438A (ja) * 2013-05-01 2014-11-20 富士フイルム株式会社 液晶表示装置
US20150168779A1 (en) * 2013-12-17 2015-06-18 Samsung Sdi Co., Ltd. Module for liquid crystal displays and liquid crystal display including the same
JP2015141346A (ja) * 2014-01-29 2015-08-03 東洋紡株式会社 液晶表示装置及び偏光板
JP2016504632A (ja) * 2013-01-11 2016-02-12 ドングウー ファイン−ケム カンパニー、 リミテッドDongwoo Fine−Chem Co., Ltd. 液晶表示装置

Family Cites Families (35)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3909794B2 (ja) * 1999-09-29 2007-04-25 富士フイルム株式会社 ポリエステルフィルムの製造方法
US7084944B2 (en) * 2000-05-15 2006-08-01 Fuji Photo Film Co., Ltd. Optical compensatory sheet comprising a biaxially stretched cellulose acetate film, polarizing plate and liquid crystal display
JP2002006133A (ja) * 2000-06-19 2002-01-09 Nitto Denko Corp 偏光子、偏光板及びそれを用いた液晶表示装置
TWI245147B (en) * 2000-06-19 2005-12-11 Nitto Denko Corp Polarizing plate and liquid crystal display using the same
JP2002207123A (ja) * 2001-01-11 2002-07-26 Nitto Denko Corp 位相差板の製造部材、位相差板の製造方法、光学部材、照明装置及び液晶表示パネル
JP2003075637A (ja) * 2001-09-05 2003-03-12 Nitto Denko Corp 位相差フィルム及びそれを用いた自発光型表示装置
US7038744B2 (en) * 2002-01-09 2006-05-02 Konica Corporation Polarizing plate having a stretched film on a side thereof and liquid crystal display employing the same
KR100777960B1 (ko) * 2002-02-19 2007-11-21 닛토덴코 가부시키가이샤 광학보상기능 편광판 및 그것을 사용한 액정표시장치
JP2004226799A (ja) * 2003-01-24 2004-08-12 Konica Minolta Holdings Inc 偏光板保護フィルム、偏光板及び画像表示用材料
JP4232004B2 (ja) * 2003-03-11 2009-03-04 三菱樹脂株式会社 二軸配向ポリエステルフィルム
KR100978951B1 (ko) * 2003-12-05 2010-08-31 엘지디스플레이 주식회사 액정표시장치용 액정패널
CN1954023B (zh) * 2004-05-14 2010-06-16 富士胶片株式会社 光学纤维素酰化物膜、起偏振板和液晶显示装置
JP3841306B2 (ja) * 2004-08-05 2006-11-01 日東電工株式会社 位相差フィルムの製造方法
JP2006267503A (ja) 2005-03-23 2006-10-05 Fuji Photo Film Co Ltd 画像表示装置
JP2007119717A (ja) * 2005-04-22 2007-05-17 Fujifilm Corp セルロースアシレートフィルム、偏光板及び液晶表示装置
US20080049323A1 (en) * 2006-07-27 2008-02-28 Fujifilm Corporation Optical film, production method of optical film, polarizing plate and liquid crystal display device
CN101910890A (zh) * 2008-01-08 2010-12-08 住友化学株式会社 偏振板
CN102955286B (zh) * 2011-08-23 2016-07-06 富士胶片株式会社 液晶显示器
JP5461640B2 (ja) * 2011-09-05 2014-04-02 日東電工株式会社 保護フィルムおよび保護フィルム付偏光板
JP2014006505A (ja) * 2012-05-10 2014-01-16 Fujifilm Corp 液晶表示装置
JP6194179B2 (ja) * 2012-10-04 2017-09-06 富士フイルム株式会社 液晶表示装置
JP5941832B2 (ja) * 2012-10-04 2016-06-29 富士フイルム株式会社 光学フィルム、位相差フィルム、偏光板及び液晶表示装置
WO2014057949A1 (ja) * 2012-10-12 2014-04-17 富士フイルム株式会社 液晶表示装置
KR102062556B1 (ko) * 2012-11-26 2020-01-06 엘지디스플레이 주식회사 곡면형 패널 및 이를 이용한 액정표시장치
JP2014209162A (ja) * 2013-03-28 2014-11-06 富士フイルム株式会社 偏光板及び画像表示装置
JP6664866B2 (ja) * 2013-04-05 2020-03-13 住友化学株式会社 偏光板のセット及び前面板一体型液晶表示パネル
JP2014206702A (ja) * 2013-04-16 2014-10-30 富士フイルム株式会社 偏光板及び画像表示装置
JP6096582B2 (ja) * 2013-04-19 2017-03-15 富士フイルム株式会社 偏光板及びその製造方法ならびに画像表示装置
KR101533883B1 (ko) 2013-06-18 2015-07-03 주식회사 엘지화학 편광판 및 이를 포함하는 디스플레이 장치
JP6617561B2 (ja) * 2013-12-18 2019-12-11 東レ株式会社 積層ポリエステルフィルム、及び、それを用いた偏光板
KR101669320B1 (ko) * 2013-12-20 2016-10-25 제일모직주식회사 액정표시장치용 모듈 및 이를 포함하는 액정표시장치
KR101938411B1 (ko) * 2014-01-13 2019-01-15 동우 화인켐 주식회사 편광판
JP2015232121A (ja) * 2014-05-16 2015-12-24 東レ株式会社 光学用ポリエステルフィルム及びそれを用いた偏光板、透明導電性フィルム
WO2015190190A1 (ja) * 2014-06-11 2015-12-17 コニカミノルタ株式会社 液晶表示装置
JP6314228B2 (ja) * 2014-07-18 2018-04-18 富士フイルム株式会社 一軸配向ポリエステルフィルム、ハードコートフィルム、タッチパネル用センサーフィルム、飛散防止フィルム、反射防止フィルム、タッチパネルおよび一軸配向ポリエステルフィルムの製造方法

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010032718A (ja) * 2008-07-28 2010-02-12 Nitto Denko Corp 液晶パネル及び液晶表示装置
WO2013187134A1 (ja) * 2012-06-11 2013-12-19 富士フイルム株式会社 液晶表示装置
JP2016504632A (ja) * 2013-01-11 2016-02-12 ドングウー ファイン−ケム カンパニー、 リミテッドDongwoo Fine−Chem Co., Ltd. 液晶表示装置
JP2014219438A (ja) * 2013-05-01 2014-11-20 富士フイルム株式会社 液晶表示装置
US20150168779A1 (en) * 2013-12-17 2015-06-18 Samsung Sdi Co., Ltd. Module for liquid crystal displays and liquid crystal display including the same
JP2015141346A (ja) * 2014-01-29 2015-08-03 東洋紡株式会社 液晶表示装置及び偏光板

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2020091494A (ja) * 2017-09-15 2020-06-11 東洋紡株式会社 偏光子保護フィルム、偏光板及び液晶表示装置
JP7322736B2 (ja) 2017-09-15 2023-08-08 東洋紡株式会社 偏光子保護フィルム、偏光板及び液晶表示装置
CN111712742A (zh) * 2018-06-29 2020-09-25 株式会社Lg化学 偏光板、液晶面板和显示装置
JP2021513111A (ja) * 2018-06-29 2021-05-20 エルジー・ケム・リミテッド 偏光板、液晶パネルおよびディスプレイ装置
JP2021513116A (ja) * 2018-06-29 2021-05-20 エルジー・ケム・リミテッド 偏光板、液晶パネルおよびディスプレイ装置
US11650362B2 (en) 2018-06-29 2023-05-16 Lg Chem, Ltd. Polarizing plate, liquid crystal panel and display device
KR20200034521A (ko) * 2018-09-21 2020-03-31 주식회사 엘지화학 액정 표시 장치
JP2021512368A (ja) * 2018-09-21 2021-05-13 エルジー・ケム・リミテッド 液晶表示装置
KR102275734B1 (ko) * 2018-09-21 2021-07-08 주식회사 엘지화학 액정 표시 장치
US11209693B2 (en) 2018-09-21 2021-12-28 Lg Chem, Ltd. Liquid crystal display
JP7282398B2 (ja) 2018-09-21 2023-05-29 エルジー・ケム・リミテッド 液晶表示装置
US20210356640A1 (en) * 2019-01-11 2021-11-18 Lg Chem, Ltd. Polarizing plate

Also Published As

Publication number Publication date
CN109073929B (zh) 2021-04-23
KR20200040922A (ko) 2020-04-20
KR102311948B1 (ko) 2021-10-13
KR20180124974A (ko) 2018-11-21
JP6205089B1 (ja) 2017-09-27
KR102502207B1 (ko) 2023-02-21
CN111443417A (zh) 2020-07-24
JP7238238B2 (ja) 2023-03-14
TW201738636A (zh) 2017-11-01
JP2017194717A (ja) 2017-10-26
JP2022000701A (ja) 2022-01-04
CN111443417B (zh) 2023-05-23
KR20210125608A (ko) 2021-10-18
KR102312023B1 (ko) 2021-10-13
JPWO2017170216A1 (ja) 2018-04-05
CN109073929A (zh) 2018-12-21
TWI729104B (zh) 2021-06-01

Similar Documents

Publication Publication Date Title
JP6205089B1 (ja) 液晶表示装置
JP6708996B2 (ja) 偏光子保護フィルム、偏光板及び液晶表示装置
US20230192974A1 (en) Polyester film and use thereof
JP7024934B1 (ja) 偏光子保護用ポリエステルフィルム、偏光板及び液晶表示装置
WO2024058058A1 (ja) ポリエステルフィルムとその用途
WO2023248877A1 (ja) 偏光子保護用ポリエステルフィルム、偏光板及び液晶表示装置

Legal Events

Date Code Title Description
ENP Entry into the national phase

Ref document number: 2017531407

Country of ref document: JP

Kind code of ref document: A

NENP Non-entry into the national phase

Ref country code: DE

ENP Entry into the national phase

Ref document number: 20187030586

Country of ref document: KR

Kind code of ref document: A

121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 17774753

Country of ref document: EP

Kind code of ref document: A1

122 Ep: pct application non-entry in european phase

Ref document number: 17774753

Country of ref document: EP

Kind code of ref document: A1