US20050151890A1 - Optical film and process for producing the same - Google Patents

Optical film and process for producing the same Download PDF

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Publication number
US20050151890A1
US20050151890A1 US10/508,828 US50882804A US2005151890A1 US 20050151890 A1 US20050151890 A1 US 20050151890A1 US 50882804 A US50882804 A US 50882804A US 2005151890 A1 US2005151890 A1 US 2005151890A1
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Prior art keywords
thermoplastic resin
film
optical film
cooling drum
temperature
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US10/508,828
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English (en)
Inventor
Koichi Nishimura
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Zeon Corp
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Zeon Corp
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Assigned to ZEON CORPORATION reassignment ZEON CORPORATION ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: NISHIMURA, KOICHI
Publication of US20050151890A1 publication Critical patent/US20050151890A1/en
Priority to US12/021,984 priority Critical patent/US7785503B2/en
Abandoned legal-status Critical Current

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Classifications

    • GPHYSICS
    • G02OPTICS
    • G02BOPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B5/00Optical elements other than lenses
    • G02B5/30Polarising elements
    • G02B5/3083Birefringent or phase retarding elements
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/03Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the shape of the extruded material at extrusion
    • B29C48/07Flat, e.g. panels
    • B29C48/08Flat, e.g. panels flexible, e.g. films
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/25Component parts, details or accessories; Auxiliary operations
    • B29C48/88Thermal treatment of the stream of extruded material, e.g. cooling
    • B29C48/911Cooling
    • B29C48/9135Cooling of flat articles, e.g. using specially adapted supporting means
    • B29C48/914Cooling of flat articles, e.g. using specially adapted supporting means cooling drums
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/25Component parts, details or accessories; Auxiliary operations
    • B29C48/88Thermal treatment of the stream of extruded material, e.g. cooling
    • B29C48/918Thermal treatment of the stream of extruded material, e.g. cooling characterized by differential heating or cooling
    • B29C48/9185Thermal treatment of the stream of extruded material, e.g. cooling characterized by differential heating or cooling in the direction of the stream of the material
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J5/00Manufacture of articles or shaped materials containing macromolecular substances
    • C08J5/18Manufacture of films or sheets
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/001Combinations of extrusion moulding with other shaping operations
    • B29C48/0018Combinations of extrusion moulding with other shaping operations combined with shaping by orienting, stretching or shrinking, e.g. film blowing
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/16Articles comprising two or more components, e.g. co-extruded layers
    • B29C48/18Articles comprising two or more components, e.g. co-extruded layers the components being layers
    • B29C48/23Articles comprising two or more components, e.g. co-extruded layers the components being layers with means for avoiding adhesion of the layers, e.g. for forming peelable layers
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/25Component parts, details or accessories; Auxiliary operations
    • B29C48/88Thermal treatment of the stream of extruded material, e.g. cooling
    • B29C48/918Thermal treatment of the stream of extruded material, e.g. cooling characterized by differential heating or cooling
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29KINDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
    • B29K2995/00Properties of moulding materials, reinforcements, fillers, preformed parts or moulds
    • B29K2995/0037Other properties
    • B29K2995/0072Roughness, e.g. anti-slip
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2323/00Functional layers of liquid crystal optical display excluding electroactive liquid crystal layer characterised by chemical composition
    • C09K2323/03Viewing layer characterised by chemical composition
    • C09K2323/031Polarizer or dye

Definitions

  • the present invention relates to an optical film suitably used as a variety of films used in a flat panel display, etc. and a raw material film thereof, a production method of the optical film, a protective film of a polarizer composed of the optical film, a polarizing film having the protective film and a phase difference film obtained by performing stretch processing on the optical film.
  • phase plate those obtained by stretching a raw material film, such as polycarbonate, giving a certain amount of retardation (also referred to as a phase difference) thereto, and putting two or more of them together are mainly used.
  • polarizing plate those obtained by stacking a protective film on an upper surface and a lower surface of a polarizer made by polyvinyl alcohol are mainly used.
  • protective film of a polarizer a film obtained by a solution casting method of triacetyl cellulose is mainly used.
  • liquid crystal substrate film a film made by polyethylene terephthalate (PET) is mainly used.
  • thermoplastic resin films have been required to have highly less optical distortion than those in the conventional ones. It is because when the optical distortion is large, optical defects, such as color unevenness and color absence, etc., allover the flat panel display are caused.
  • an amount of retardation has been mainly used.
  • an effort to diminish the optical distortion has been made.
  • a polarizer protective film having a small and constant retardation amount allover the film has been its index.
  • a film made by a solution casting method of triacetyl cellulose (TAC) has been mainly used.
  • a solution casting method film of TAC has a relatively small retardation being relatively constant on a film surface.
  • a solvent cannot be completely removed at the time of drying after the solution casting, and an emitted solvent gives an adverse effect on an electronic circuit and other parts of the flat panel display to cause an erroneous operation and display defective, etc.
  • the Japanese Unexamined Patent Publication No. 2000-273204 discloses a technique of obtaining a sheet having a sheet thickness of 150 to 1000 ⁇ m, in-plane thickness tolerance (Rmax) on the sheet of 15 ⁇ m, roughness of the sheet surface of 0.06 ⁇ m, and a retardation amount (maximum value) on the sheet surface of 15 nm, wherein a retardation amount is relatively constant and relatively small by performing melt extrusion molding on a specific thermoplastic resin under a specific condition.
  • An object of the present invention is to provide an optical film having no residual solvent problem, small optical distortion, and no problem of color unevenness and color absence of a liquid display to be obtained when used as a polarizer protective film, a process for producing the optical film, a polarizer protective film configured by the optical film, a polarizing film having the protective film, and a phase difference film with small optical distortion obtained by performing stretch processing on the optical film.
  • the present inventors have been committed themselves to study for solving the above problems, consequently, found a technique of making a retardation amount (Re) of an optical film to be obtained to be 10 nm or less by optimizing a melt extrusion condition and an operation condition of cooling drums, and completed as another invention.
  • the maximum value of Re becomes 0 nm, it means there is no in-plane optical distortion.
  • the maximum value of Re is hardly made to be a certain level or less and there is a limit.
  • the present inventors focused not only on the Re value but on the direction of a slow phase axis indicating directivity. At each point, the direction that birefringent becomes maximum is referred to as a slow phase axis, and the direction that the birefringent becomes minimum is referred to as a fast phase axis.
  • the present invention was completed based on the knowledge.
  • a value of said Re is 10 nm or less.
  • thermoplastic resin is an alicyclic structure containing polymer.
  • the optical film according to the present invention is preferably produced, for example, by a production method below.
  • thermoplastic resin when assuming a resin contact time in said first cooling drum is t 1 (sec.), a temperature when said thermoplastic resin moves away from said first cooling drum is Tp 1 (° C.), and a glass transition temperature of said thermoplastic resin is Tg (° C.), t 1 ⁇ (Tp 1 ⁇ Tg) (unit: sec. ⁇ deg) is made to be ⁇ 50 or higher and 20 or lower to cool said thermoplastic resin.
  • a ratio of the R 2 and R 1 is made to be 0.990 or more but less than 1.01 to cool said thermoplastic resin.
  • thermoplastic resin moves away from said third cooling drum is Tp 3 (° C.) the Tp 3 is made to be a lower temperature than said Tg by 50 to 100° C. to cool said thermoplastic resin.
  • thermoplastic resin moves away from said second cooling drum is Tp 2 (° C.)
  • Tp 2 a temperature when said thermoplastic resin moves away from said second cooling drum
  • the Tp 2 is made to be a lower temperature than said Tg by 0 to 60° C. to cool said thermoplastic resin.
  • a temperature difference of said first cooling drum and said second cooling drum is made to be 20° C. or less to cool said thermoplastic resin.
  • a protective film of a polarizer composed of any one of the above optical films.
  • a polarizing film having a polarizer and the above protective film stacked on one surface or both surfaces of the polarizer via an adhesive layer.
  • phase difference film obtained by performing stretch processing on any one of the above optical films.
  • An optical film according to the present invention is configured by a thermoplastic resin film.
  • thermoplastic resin film used in the present invention includes at least a thermoplastic resin.
  • the thermoplastic resin is not particularly limited as far as it is a resin normally used in producing an optical film.
  • polyethylene, polypropylene, an ethylene-propylene copolymer, polystyrene, polyacrylonitrile, an acrylonitrile-styrene copolymer, polyvinylchloride, polymethyl methacrylate, polyethylene terephthalate, polybutylene terephthalate, polycarbonate and an alicyclic structure containing polymer, etc. may be mentioned.
  • polyethylene terephthalate, polybutylene terephthalate and an alicyclic structure containing polymer are preferable and, furthermore, an alicyclic structure containing polymer is particularly preferable because a phase difference is easily made small.
  • An alicyclic structure containing polymer is a polymer having a cyclic structure made by carbon-carbon saturated bonds (referred to as “an alicyclic structure” in the present invention) in a repeat unit and, for example, a well-known polymer disclosed in the Japanese Unexamined Patent Publication No. 2002-321302 may be used.
  • ring-opened polymers and the hydrogenated products of monomers having a norbornene ring (hereinafter, referred to as “norbornene”), addition polymers of norbornene and the hydrogenated products, addition copolymers of norbornene and a vinyl compound and the hydrogenated products; polymers obtained by hydrogenating aromatic ring of a polymer of polystyrene or other aromatic vinyl hydrocarbon compounds, addition polymers of monomers having an alicyclic structure and a vinyl group, addition polymers of monomers having one or more unsaturated bonds in a carbon-carbon cyclic structure and the hydrogenated products, etc. may be mentioned.
  • the thermoplastic resin film used in the present invention may be blended with a variety of compounding agents in accordance with need other than the above thermoplastic resins.
  • the compounding agents are not particularly limited. For example, antioxidants, heat stabilizers, light stabilizers, weather resistant stabilizers, ultraviolet ray absorbents, near infrared ray absorbents and other stabilizers; lubricants, plasticizers and other resin improvers; colorants, pigments and other coloring agents; antistatic agents, etc. may be mentioned.
  • These compounding agents may be used alone or in combination of two or more kinds.
  • a blending quantity of these compounding agents is suitably selected in a range of not hindering the objects of the present invention.
  • antioxidants As antioxidants, phenol based antioxidants, phosphorus based antioxidants, and sulfur based antioxidants, etc. may be mentioned. Among these, phenol based antioxidants are preferable and alkyl-substituted phenol based antioxidants are particularly preferable.
  • the antioxidants may be used alone or in combination of two or more kinds.
  • a blending quantity of antioxidants is suitably selected in a range of not hindering the object of the present invention. Normally, it is 0.001 to 5 parts by weight or so and preferably 0.01 to 1 part by weight with respect to 100 parts by weight of a thermoplastic resin.
  • the thermoplastic resin film used in the present invention is produced by performing melt extrusion molding on a molding material including at least a thermoplastic resin. Specifically, first, a molding material is obtained by, for example, mixing a thermoplastic resin and a variety of compounding agents. Next, the molding material is processed to be material pellets suitable for melt extrusion molding. Next, the material pellets are supplied to a melt extruding machine and processed to be a film shape by a melt extrusion method to obtain a thermoplastic resin film.
  • the melt extrusion method is a method of heating and melting the material pellets in a cylinder, applying pressure by a screw, and extruding from a die, such as T-die, to be, for example, a film shape.
  • thermoplastic resin in a molten state extruded from a die is successively transferred by being circumscribed with a plurality of cooling drums, cooled during that time, then, subjected to necessary steps to be a thermoplastic resin film.
  • a width of the thermoplastic resin film after passing through the cooling drums becomes narrower by 2 to 10% due to neck-in comparing with a width of a molten thermoplastic resin immediately after being extruded from a die (same as a width of a lip of the die).
  • An end of the thermoplastic resin film in the width direction (hereinafter., also simply referred to as “an end”) has a thicker thickness and larger optical distortion comparing with those on other parts of the film.
  • thermoplastic resin film after cooling is for an optical use
  • sides thereof are suitably cut off before winding with a wind drum.
  • the cut off parts will be called “selvage” in the present invention.
  • a part of the cooled thermoplastic resin film yet to be stretched after removing parts to be the selvage will be referred to as “an optical film” in the present invention.
  • an optical film As in a protective film and a liquid crystal substrate, etc., when used in a state that a retardation amount is nearly zero, selvage is removed from the thermoplastic resin film yet to be stretched, the optical film is taken out and wound by a wind drum.
  • thermoplastic resin film used in the present invention is made to be an optical film, wound to be a roll shape by a wind drum, then, it may be subjected to the next step: a stretch step and an adhesion step to other film, etc. to be value-added.
  • An average thickness of the thermoplastic resin film used in the present invention is not particularly limited. To make an optical film taken out from the thermoplastic resin film used in the present invention suitable to a thin flat panel display, etc., it is preferable that an average thickness of the thermoplastic resin film is made to be normally 100 ⁇ m or less, preferably 80 ⁇ m or less, particularly preferably 60 ⁇ m or less. An average thickness of the thermoplastic resin film can be freely set by changing a feeding speed of the material pellets fed to the melt extrusion machine or a rotation speed of the cooling drum or the both, etc.
  • thermoplastic resin film used in the present invention satisfies the relation of the formula below on the whole surface of the film when assuming that an angle made by the extruding direction from the melt extrusion machine and a slow phase axis at each point is ⁇ , and a retardation amount at each point is Re. [sin 2 2 ⁇ ] ⁇ [sin 2 ( ⁇ Re/ 550)] ⁇ 4.0 ⁇ 10 ⁇ 5
  • the left side of the equation [sin 2 2 ⁇ ] ⁇ [sin 2 ( ⁇ Re/550)] is referred to as a Z value.
  • the Z value is an amount corresponding to light leakage caused by retardation of the optical film.
  • Linear polarization cannot transmit a polarizer having an absorption axis perpendicular to the light axis.
  • the linear polarization transmits the optical film with optical distortion (retardation is not zero)
  • a phase delays in the slow phase axis direction of the optical film and a part of the linear polarization can transmit the polarizer.
  • color unevenness and color absence are caused in a liquid crystal display using the optical film.
  • is normally defined as an angle made by a slow phase axis of the film and a light axis of linear polarization.
  • cannot be defined. Therefore, the present inventors focused on an angle made by the extruding direction of the thermoplastic resin film to be an optical film from the melt extruding machine and a slow phase axis at each point, and used the same as a to define a Z value for an alternative characteristic.
  • a maximum value of the Z value can be obtained by measuring over a suitable longitudinal length and measuring points including a part close to an end of the optical film in the width direction.
  • the value can be applied as a substitute value.
  • the maximum value of the Z value is normally required to be 4.0 ⁇ 10 ⁇ 5 , preferably 3.8 ⁇ 10 ⁇ 5 , and furthermore preferably 3.4 ⁇ 10 ⁇ 5 .
  • the Z value is a predetermined value or less, a problem of color unevenness and color absence of a liquid crystal display to be obtained becomes furthermore smaller, and color unevenness and color absence are not visually sensed, so that the display quality is remarkably improved, which is preferable.
  • the maximum value of Re is not particularly limited.
  • Re over whole surface of the film is preferably 10 nm or less, more preferably 7 nm or less, and furthermore preferably 5 nm or less.
  • the Re value is a predetermined value or less, a problem of color unevenness and color absence of a liquid crystal display to be obtained becomes furthermore smaller. Also, color unevenness and color absence after a durability test become furthermore smaller, which is preferable.
  • the Re value can be measured by an optical method, such as an ellipsometer.
  • an optical method such as an ellipsometer.
  • a value obtained by measuring over a suitable longitudinal length and measuring points including a part close to an end of the optical film in the width direction can be applied as a substitute value.
  • a method of producing an optical film according to the present invention which satisfies the above conditions is not particularly limited.
  • a method of increasing a ratio of the selvage part to the whole film so as to satisfy the above conditions on the whole surface of the film may be mentioned.
  • the ratio of the selvage part in this case is normally 3% or more on the right and the left, preferably 5% or more on the right and the left, particularly preferably 7% or more on the right and the left, preferably 40% or less on the right and the left, and particularly preferably 20% or less on the right and the left.
  • an optical film of the present invention can be also produced by optimizing the conditions from melt extrusion to winding of the thermoplastic resin film.
  • a production method of an optical film according to the present invention includes a step of cooling a molten thermoplastic resin extruded from an extruding machine by making it circumscribed with a first cooling drum, second cooling drum and third cooling drum successively. After that, more preferably, a step of cutting both end portions in the width direction of the cooled thermoplastic resin, and a step of winding the cut thermoplastic resin in a roll shape are included.
  • thermoplastic resin is cooled to satisfy preferably at least any one of (1) to (6) below, more preferably at least (1) and (2) below, and particularly preferably all of (1) to (6) below.
  • the ratio of the R 3 and R 2 (R 3 /R 2 ) is made to be preferably 0.990 or more but less than 0.999, and more preferably 0.995 or more but less than 0.998 to cool the thermoplastic resin.
  • a sheet thermoplastic resin a molten thermoplastic resin extruded from the extruding machine
  • the resin temperature is set to be appropriate for a contraction percentage of the resin caused by a temperature decline from around the second cooling drum temperature to around the third cooling drum temperature when transferring the sheet thermoplastic resin from the second cooling drum to the third cooling drum.
  • t 1 ⁇ (Tp 1 ⁇ Tg) (unit: sec. ⁇ deg) is made to be preferably ⁇ 50 or higher and 20 or lower, and more preferably ⁇ 40 or higher and +15 or lower to cool the thermoplastic resin.
  • the ratio of R 2 and R 1 is preferably set to 0.990 or more but less than 1.01, and more preferably 0.995 or more but less than 1.000 to cool the thermoplastic resin.
  • R 2 /R 1 is in the ranges, unevenness of a retardation amount of an optical film to be obtained becomes particularly small, and wrinkles when winding is hard to arise.
  • the Tp 3 is set to be lower than the above Tg preferably by 50 to 100° C., and more preferably by 60 to 80° C. to cool the thermoplastic resin.
  • Tg a temperature when the thermoplastic resin moves away from the third cooling drum
  • the value of the Tp 3 is in the ranges, unevenness of a retardation amount of an optical film to be obtained becomes particularly small, and wrinkles when winding is hard to arise.
  • the Tp 2 is set to be lower than the above Tg preferably by 0 to 60° C., and more preferably by 20 to 40° C. to cool the thermoplastic resin.
  • the value of the Tp 2 is in the ranges, unevenness of a retardation amount of an optical film to be obtained becomes particularly small, and wrinkles when winding is hard to arise.
  • a temperature difference of the first cooling drum and the second cooling drum is made to be preferably 20° C. or less, and more preferably 10° C. or less to cool the thermoplastic resin.
  • the optical film according to the present invention is suitable as a protective film of a polarizer of a liquid crystal display.
  • the polarizer is obtained by performing stretch processing after doping with iodine on a film made by a vinyl alcohol based polymer, such as polyvinyl alcohol and partially formalization polyvinyl alcohol.
  • the optical film of the present invention is staked as a protective film on one surface or both surfaces of the polarizer via a suitable adhesive layer, so that a polarizing film can be obtained.
  • a suitable adhesive layer an adhesive agent, etc. wherein a suitable polymer is a base polymer, such as an acryl based polymer, a silicon based polymer, polyester, polyurethane, polyether, and synthetic rubber is used.
  • the optical film of the present invention is suitable to a material for producing a polarizing film as a protective film by putting the longitudinal direction together with the longitudinal direction of a long polarizer (referred to as roll-to-roll), and adhering to stack.
  • the optical film of the present invention may be furthermore subjected to stretch processing to obtain a phase difference film.
  • a phase difference film is a film having a uniform retardation amount of a predetermined value over the whole surface of the phase difference film.
  • a tenter is used for performing stretch processing on the optical film of the present invention.
  • a film temperature during stretching is, for example, (Tg ⁇ 100)° C. or higher and (Tg +40)° C. or lower.
  • Tg is a glass transition temperature of a thermoplastic resin to be a material.
  • the stretching ratio depends on a retardation value to be obtained and a thickness of the phase difference film, it is normally 1.05 times or more and 3.0 times or less in the length direction (extruding direction of the thermoplastic resin film) and 0.2 times or less in the width direction, or may be uniaxially stretched in the length direction.
  • film thickness was obtained by measuring at every 500 mm over 10 m in the film length direction (20 points) and at 5 points at regular intervals in the width direction (unit: ⁇ m).
  • ⁇ and Re (unit:nm) were measured at every 500 mm over 10 m in the film length direction (20 points) and at 5 points at regular intervals in the width direction, a Z value was calculated from the results, and the maximum values of Re and Z value were obtained from the values.
  • a measurement wavelength was set to be 550 nm and an incident angle was 0°.
  • the whole light transmittance of the optical film was measured by the cross Nicole method based on JIS-K7105, and the average value was obtained (unit: %).
  • the value is ideally 0, but preferable when 0.03% or less and defective when 0.04% or more.
  • the measurement points in the present invention were at every 500 mm over 10 m in the film length direction and at 10 points at regular intervals in the width direction.
  • a polarizing film was peeled from a liquid crystal cell very carefully on a display portion of a cellular phone on market (black and white two-graduation display, reflection type, a display area of 30 mm ⁇ 30 mm), and a polarizing film produced by using the optical film of the present invention was stacked as a protective film on both surfaces of the polarizer to produce a test liquid crystal display.
  • a part close to the end of the optical film in the width direction was used as a sample piece, and 10 mass % of polyvinyl alcohol solution was used for stacking.
  • the above test liquid crystal display was produced for each experiment example, a variety of characters and still images were displayed, and observed from viewable angles of 0° and 30° to visually observe existence of color unevenness and color absence (a part where a proper color is not displayed). Those at an approvable level were marked ⁇ , defectives were marked x, and those in the middle and not at an approvable level were marked ⁇ .
  • a test piece of 1000 mm ⁇ 1000 mm was cut from the obtained optical film, and a high temperature high humidity durability promotion test at 80° C. and 90% RH for 100 hours was conducted thereon. After that, the same color unevenness test as that in (4) was conducted on the taken out test piece.
  • cyclohexane and other volatile components were removed from the solution by using a cylinder shaped concentrating and drying device (made by Hitachi Ltd.), a molten hydrogenated polymer was extruded to be a strand shape from an extruding machine, cooled and pelletized to obtain a ring-opened polymer hydrogenate.
  • the hydrogenate had a glass transition temperature,Tg of 140° C.
  • the obtained pellets are subjected to melt extrusion by a single-screw extrusion molding machine (made by Japan Steel Works Ltd.) having a cylinder inner diameter of 50 mm and a screw L/D value of 28 at a barrel temperature of 260° C., and a sheet molten resin having a width of 650 mm was extruded from a coat hunger die at a die temperature of 260° C.
  • the result was made close to a first cooling drum (diameter of 200 mm, temperature T 1 of 135° C., rotation speed R 1 of 14.50 m/min.), immediately transferred by a knife coater from the first cooling drum, then, to a second cooling drum (diameter of 350 mm, temperature T 2 of 125° C., rotation speed R 2 of 14.46 m/min.), then, to a third cooling drum (diameter of 350 mm, temperature T 3 of 80° C., rotation speed R 3 of 14.40 m/min.) successively, and cooling and smoothing of the front and back surfaces by transferring the cool drum surfaces were sequentially performed to obtain a thermoplastic resin film having a width of 550 mm (the neck-in was 50 mm on the right and the left). The thermoplastic resin film passed through an adjustment drum, then, 30 mm was removed as selvage from both ends by a cutter, the result was wound in a roll shape by a wind drum, and a rolled optical film was obtained.
  • a contact time t 1 of the sheet thermoplastic resin with the first cooling drum was 3.1 (seconds)
  • a resin temperature Tp 1 when moving away from the first cooling drum was 132 (° C.)
  • a resin temperature Tp 2 when moving away from the second cooling drum was 119 (° C.)
  • a resin temperature Tp 3 when moving away from the third cooling drum was 79 (° C.).
  • (R 3 /R 2 ) 0.996
  • (R 2 /R 1 ) 0.997
  • (t 1 ⁇ (Tp 1 ⁇ Tg)) ⁇ 25 (unit: sec. ⁇ deg).
  • the optical films of examples of the present invention have a small Z value comparing with those in the comparative examples, so that they are excellent in the whole light transmittance, polarization degree, color unevenness and color unevenness after a durability test.
  • the maximum Re values are smaller than the result of the example 4, so that color unevenness and results of the simple liquid crystal display test are excellent.
  • the Z values are smaller than those in the results of the examples 4 and 5, so that color unevenness after a durability test is excellent.
  • the optical film obtained in the present invention can be made to be a phase difference film by performing stretch processing thereafter.
  • a phase difference film is required to have a predetermined phase difference (retardation value), and the value has to be uniform.
  • a test below was conducted.
  • An obtained optical film obtained in the experiment was cut out to be a test piece (a width of 100 mm and a length of 150 mm), and the test piece was stretched at 140° C. by 1.1 to 2 times in the longitudinal direction at a speed of 100 mm/min. The stretching ratio was adjusted so that an average retardation becomes 275 ⁇ 10 nm.
  • the retardation was measured by the same measurement method as that in the (2), and Re unevenness was obtained by dividing unevenness (difference between the maximum value and the minimum value) by an average value.
  • the measurement points were at a center portion in the width direction and 10 points at every 10 mm near the center in the length direction.
  • Table 3 shows results of measuring Re unevenness after stretching in respective examples. TABLE 3 Result of Re Unevenness Test after Stretching Comparative Comparative Example 1 Example 2 Example 3 Example 4 Example 5 Example 1 Example 2 Re Unevenness Test 1.8 2.2 2.1 2.6 2.1 5.8 6.6 after Stretching (%)
  • the optical films of the examples of the present invention have smaller Z values than those in the case of comparative examples, so that retardation unevenness after stretch processing is small, which is excellent.
  • the optical film of the present invention is suitable as a raw material film of a phase difference film.
  • the optical film of the present invention is useful as a variety of optical films of a flat panel display, such as a protective film of a polarizer and a liquid crystal cell substrate film. Also, the optical film of the present invention has small and uniform retardation, and it can be made to be a phase difference film having a predetermined uniform retardation by performing stretch processing after that. Therefore, the optical film of the present invention is useful as a raw material film of a phase difference film, etc.

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Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20060164591A1 (en) * 2005-01-21 2006-07-27 Seiko Epson Corporation Film formation method, electro-optical device manufacturing method and electronic apparatus
US20070039543A1 (en) * 2005-08-20 2007-02-22 Schuster Karl H Phase delay element and method for producing a phase delay element
US20090209720A1 (en) * 2006-10-11 2009-08-20 Yasuhara Chemical Co., Ltd. Beta-PINENE POLYMER AND PROCESS FOR PRODUCING THE SAME
US20100118399A1 (en) * 2008-11-12 2010-05-13 Nitto Denko Corporation Method for producing polarizing plate, polarizing plate, optical film, and image display
US20110032453A1 (en) * 2009-08-05 2011-02-10 Moon Chang Yul Diffusion sheet and liquid crystal display device with the same
US10228782B2 (en) 2013-03-04 2019-03-12 Fujifilm Corporation Transparent conductive film and touch panel

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005156734A (ja) * 2003-11-21 2005-06-16 Fuji Photo Film Co Ltd 偏光板、およびそれを用いた液晶表示装置
KR101229502B1 (ko) * 2004-09-24 2013-02-04 후지필름 가부시키가이샤 셀룰로오스 아실레이트 막, 그 제조방법, 연신된셀룰로오스 아실레이트 막 및 그 제조방법
US7339635B2 (en) * 2005-01-14 2008-03-04 3M Innovative Properties Company Pre-stacked optical films with adhesive layer
JP2006218611A (ja) * 2005-02-14 2006-08-24 Sumitomo Bakelite Co Ltd 微細流路を有するプラスチック製品
JP4720393B2 (ja) * 2005-09-20 2011-07-13 コニカミノルタオプト株式会社 光学フィルムの製造方法
CN101460306B (zh) * 2006-03-31 2012-07-18 日本瑞翁株式会社 偏振片、液晶显示装置以及保护膜
JP2016105118A (ja) * 2013-03-22 2016-06-09 コニカミノルタ株式会社 偏光板、偏光板の製造方法及び液晶表示装置

Citations (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5516456A (en) * 1994-02-24 1996-05-14 Japan Synthetic Rubber Co., Ltd. Liquid crystal display panel
US5528400A (en) * 1994-06-08 1996-06-18 Fuji Photo Film Co., Ltd. Liquid crystal display device having negative uniaxial anisotropic film with inclined optical axis and protective films
US5543948A (en) * 1991-06-25 1996-08-06 Nippon Zeon Co., Ltd. Thermoplastic saturated norbornene resin phase plate
US20020018883A1 (en) * 2000-07-05 2002-02-14 Iwao Okazaki Thermoplastic resin film and production process thereof, and optical film
US6411344B2 (en) * 1998-06-18 2002-06-25 Kaneka Corporation Transparent touch panel and liquid crystal display device equipped with transparent touch panel
US6542300B2 (en) * 2000-10-30 2003-04-01 Nitto Denko Corporation Polarizer with composite phase compensation film
US6582789B1 (en) * 1999-10-01 2003-06-24 Teijin Limited Surface protective film and laminate formed therefrom
US6667787B2 (en) * 2000-10-30 2003-12-23 Nitto Denko Corporation Polarizer
US6731357B1 (en) * 1999-01-27 2004-05-04 Konica Corporation Cellulose ester film, production method of the same, film employed in liquid crystal display member, and polarizing plate
US6803411B2 (en) * 2000-05-02 2004-10-12 Kuraray Co., Ltd. Polyvinyl alcohol polymer film, method of producing the same and polarization film
US6808811B1 (en) * 1999-10-04 2004-10-26 Sekisui Chemical Co., Ltd. Protecting film for polarizing plate and polarizing plate
US6961180B2 (en) * 2000-11-08 2005-11-01 Nitto Denko Corporation Polarizer
US6964814B2 (en) * 1999-11-12 2005-11-15 Kaneka Corporation Transparent film

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1026349A (en) * 1961-10-27 1966-04-20 Kurashiki Rayon Kk Method of manufacturing thin films of polyvinyl alcohols
JPS60214923A (ja) * 1984-04-11 1985-10-28 Sumitomo Bakelite Co Ltd 熱可塑性樹脂フイルムの製造方法
JP3297450B2 (ja) * 1991-07-22 2002-07-02 日本ゼオン株式会社 液晶ディスプレイ用偏光フィルム
BR9608681A (pt) * 1995-05-29 1999-07-06 Hoechst Ag Placa amorfa transparente tingida de um termoplástico cristalizável processo para sua preparação assim como sua aplicação
JPH10249909A (ja) * 1997-03-11 1998-09-22 Asahi Chem Ind Co Ltd 合成樹脂シート成形ロール設備
JP3533101B2 (ja) 1999-03-19 2004-05-31 住友ベークライト株式会社 熱可塑性高分子シートの製造方法
US6881453B2 (en) * 2000-04-25 2005-04-19 Teijin Limited Optical film
JP2001337221A (ja) * 2000-05-24 2001-12-07 Sekisui Chem Co Ltd 光学用フィルム及び偏光板
JP2002321302A (ja) 2001-04-26 2002-11-05 Nippon Zeon Co Ltd 脂環式構造含有重合体樹脂積層体
JP4052846B2 (ja) 2001-10-11 2008-02-27 積水化学工業株式会社 光学フィルムの製造方法
DE60229190D1 (de) * 2001-08-10 2008-11-20 Sekisui Chemical Co Ltd Optische Kunststofffolie, Verfahren zu deren Herstellung und Polarisator

Patent Citations (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5543948A (en) * 1991-06-25 1996-08-06 Nippon Zeon Co., Ltd. Thermoplastic saturated norbornene resin phase plate
US5516456A (en) * 1994-02-24 1996-05-14 Japan Synthetic Rubber Co., Ltd. Liquid crystal display panel
US5528400A (en) * 1994-06-08 1996-06-18 Fuji Photo Film Co., Ltd. Liquid crystal display device having negative uniaxial anisotropic film with inclined optical axis and protective films
US6411344B2 (en) * 1998-06-18 2002-06-25 Kaneka Corporation Transparent touch panel and liquid crystal display device equipped with transparent touch panel
US6731357B1 (en) * 1999-01-27 2004-05-04 Konica Corporation Cellulose ester film, production method of the same, film employed in liquid crystal display member, and polarizing plate
US6582789B1 (en) * 1999-10-01 2003-06-24 Teijin Limited Surface protective film and laminate formed therefrom
US6808811B1 (en) * 1999-10-04 2004-10-26 Sekisui Chemical Co., Ltd. Protecting film for polarizing plate and polarizing plate
US6964814B2 (en) * 1999-11-12 2005-11-15 Kaneka Corporation Transparent film
US6803411B2 (en) * 2000-05-02 2004-10-12 Kuraray Co., Ltd. Polyvinyl alcohol polymer film, method of producing the same and polarization film
US20020018883A1 (en) * 2000-07-05 2002-02-14 Iwao Okazaki Thermoplastic resin film and production process thereof, and optical film
US6667787B2 (en) * 2000-10-30 2003-12-23 Nitto Denko Corporation Polarizer
US6542300B2 (en) * 2000-10-30 2003-04-01 Nitto Denko Corporation Polarizer with composite phase compensation film
US6961180B2 (en) * 2000-11-08 2005-11-01 Nitto Denko Corporation Polarizer

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20060164591A1 (en) * 2005-01-21 2006-07-27 Seiko Epson Corporation Film formation method, electro-optical device manufacturing method and electronic apparatus
US7794781B2 (en) * 2005-01-21 2010-09-14 Seiko Epson Corporation Film formation method, electro-optical device manufacturing method and electronic apparatus
US20070039543A1 (en) * 2005-08-20 2007-02-22 Schuster Karl H Phase delay element and method for producing a phase delay element
US20090209720A1 (en) * 2006-10-11 2009-08-20 Yasuhara Chemical Co., Ltd. Beta-PINENE POLYMER AND PROCESS FOR PRODUCING THE SAME
US8093344B2 (en) 2006-10-11 2012-01-10 Yasuhara Chemical Co., Ltd. β-pinene polymer and process for producing the same
US20100118399A1 (en) * 2008-11-12 2010-05-13 Nitto Denko Corporation Method for producing polarizing plate, polarizing plate, optical film, and image display
US8197629B2 (en) * 2008-11-12 2012-06-12 Nitto Denko Corporation Method for producing polarizing plate, polarizing plate, optical film, and image display
US20110032453A1 (en) * 2009-08-05 2011-02-10 Moon Chang Yul Diffusion sheet and liquid crystal display device with the same
US8755004B2 (en) * 2009-08-05 2014-06-17 Lg Display Co., Ltd. Liquid crystal display device comprising a second diffusion sheet having upper and lower diffusion layers wherein the upper diffusion layer includes multi-dispersed beads
US10228782B2 (en) 2013-03-04 2019-03-12 Fujifilm Corporation Transparent conductive film and touch panel
US10684710B2 (en) 2013-03-04 2020-06-16 Fujifilm Corporation Transparent conductive film and touch panel

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JPWO2003081299A1 (ja) 2005-11-17
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ATE513236T1 (de) 2011-07-15
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EP1496376A4 (en) 2010-04-28

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