WO2014204134A1 - Plaque polarisante mince et procédé pour sa fabrication - Google Patents

Plaque polarisante mince et procédé pour sa fabrication Download PDF

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Publication number
WO2014204134A1
WO2014204134A1 PCT/KR2014/005188 KR2014005188W WO2014204134A1 WO 2014204134 A1 WO2014204134 A1 WO 2014204134A1 KR 2014005188 W KR2014005188 W KR 2014005188W WO 2014204134 A1 WO2014204134 A1 WO 2014204134A1
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WO
WIPO (PCT)
Prior art keywords
film
polymer
polyvinyl alcohol
polarizing plate
stretching
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PCT/KR2014/005188
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English (en)
Korean (ko)
Inventor
남성현
나균일
정종현
유혜민
Original Assignee
주식회사 엘지화학
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.)
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Priority claimed from KR1020140067820A external-priority patent/KR101555782B1/ko
Application filed by 주식회사 엘지화학 filed Critical 주식회사 엘지화학
Priority to CN201480000911.2A priority Critical patent/CN104395791B/zh
Priority to US14/385,727 priority patent/US10048417B2/en
Priority to JP2015523044A priority patent/JP6173451B2/ja
Publication of WO2014204134A1 publication Critical patent/WO2014204134A1/fr

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    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00—Layered products comprising a layer of synthetic resin
    • B32B27/06—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
    • B32B27/08—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00—Layered products comprising a layer of synthetic resin
    • B32B27/30—Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00—Layered products comprising a layer of synthetic resin
    • B32B27/32—Layered products comprising a layer of synthetic resin comprising polyolefins
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00—Layered products comprising a layer of synthetic resin
    • B32B27/34—Layered products comprising a layer of synthetic resin comprising polyamides
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00—Layered products comprising a layer of synthetic resin
    • B32B27/36—Layered products comprising a layer of synthetic resin comprising polyesters
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00—Layered products comprising a layer of synthetic resin
    • B32B27/40—Layered products comprising a layer of synthetic resin comprising polyurethanes
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B7/00—Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
    • B32B7/04—Interconnection of layers
    • B32B7/12—Interconnection of layers using interposed adhesives or interposed materials with bonding properties
    • G—PHYSICS
    • G02—OPTICS
    • G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B5/00—Optical elements other than lenses
    • G02B5/30—Polarising elements
    • G02B5/3025—Polarisers, i.e. arrangements capable of producing a definite output polarisation state from an unpolarised input state
    • G02B5/3033—Polarisers, i.e. arrangements capable of producing a definite output polarisation state from an unpolarised input state in the form of a thin sheet or foil, e.g. Polaroid
    • G02B5/3041—Polarisers, i.e. arrangements capable of producing a definite output polarisation state from an unpolarised input state in the form of a thin sheet or foil, e.g. Polaroid comprising multiple thin layers, e.g. multilayer stacks
    • G02B5/305—Polarisers, i.e. arrangements capable of producing a definite output polarisation state from an unpolarised input state in the form of a thin sheet or foil, e.g. Polaroid comprising multiple thin layers, e.g. multilayer stacks including organic materials, e.g. polymeric layers
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2307/00—Properties of the layers or laminate
    • B32B2307/40—Properties of the layers or laminate having particular optical properties
    • B32B2307/402—Coloured
    • B32B2307/4026—Coloured within the layer by addition of a colorant, e.g. pigments, dyes
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2307/00—Properties of the layers or laminate
    • B32B2307/40—Properties of the layers or laminate having particular optical properties
    • B32B2307/42—Polarizing, birefringent, filtering
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2457/00—Electrical equipment
    • B32B2457/20—Displays, e.g. liquid crystal displays, plasma displays
    • B32B2457/202—LCD, i.e. liquid crystal displays
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2457/00—Electrical equipment
    • B32B2457/20—Displays, e.g. liquid crystal displays, plasma displays
    • B32B2457/206—Organic displays, e.g. OLED

Definitions

  • the present invention relates to a thin polarizing plate and a method of manufacturing the same, and more particularly, to a method of manufacturing a thin polarizing plate including a polarizer having a thin thickness of 10 ⁇ m or less, and capable of manufacturing various kinds of polarizing plates in one process. It is about.
  • the polarizer used in the polarizing plate is an optical element for making natural light or arbitrary polarization into a polarized light in a specific direction, and is widely used in a display device such as a liquid crystal display device and an organic light emitting device (OLED).
  • a polarizer used in the display device a polyvinyl alcohol polarizing film in which molecular chains containing an iodine compound or a dichroic dye are oriented in a constant direction is generally used.
  • the polyvinyl alcohol polarizing film is prepared by a method of dyeing and crosslinking iodine or dichroic dye on a polyvinyl alcohol-based film, and stretching in a predetermined direction, wherein the stretching process is an aqueous solution of boric acid or an iodine solution. It may be performed by wet stretching performed in solution or dry stretching performed in air.
  • stretching exceeds 60 micrometers.
  • polarizers are also required to have a thinner thickness.
  • a polyvinyl alcohol-based film having a thickness before stretching of more than 60 ⁇ m as in the prior art there is a limit in reducing the thickness of the polarizer. Therefore, studies have been attempted to fabricate thinner polarizers.
  • Korean Unexamined Patent Publication No. 2010-0071998 discloses a method of manufacturing a thin polarizing plate using a laminate prepared by coating a hydrophilic polymer layer on a substrate layer or co-extrusion of a substrate layer forming material and a hydrophilic polymer layer forming material. It is.
  • the separation of the polyvinyl alcohol layer and the base layer is not easy after stretching and a high peel force is required for the separation, the polyvinyl alcohol layer is damaged or deformed during the separation process. Problems tend to occur, and as a result, there is a problem that optical properties such as polarization degree of the polyvinyl alcohol film are inferior.
  • the polyvinyl alcohol resin is manufactured by melting and extruding the polyvinyl alcohol resin or by applying the coating solution after coating and then applying the polyvinyl alcohol according to extrusion conditions, coating conditions or film forming conditions.
  • the physical properties of the film tend to change, and not only the physical properties of the finally produced polyvinyl alcohol are lowered, but also it is difficult to realize uniform physical properties.
  • the present invention is to solve the above problems, to provide a thin polarizing plate having excellent optical properties, excellent curl properties, and a manufacturing method thereof having a single transmittance of 40 to 45%, a polarization degree of 99.0% or more.
  • the present invention comprises the steps of attaching a non-stretched polyvinyl alcohol-based film using a attraction force or an adhesive on the unstretched base film to form a film laminate; Stretching the film laminate; Attaching a first protective film on the polyvinyl alcohol-based film of the stretched film laminate; And it provides a method for producing a thin polarizing plate comprising the step of separating the polyvinyl alcohol-based film and the base film to which the first protective film is attached.
  • the method of manufacturing a thin polarizing plate of the present invention may further include dyeing at least one of iodine and dichroic dye on the film laminate before the stretching of the film laminate.
  • the method of manufacturing a thin polarizing plate of the present invention may further include drying the stretched film laminate after the stretching of the film laminate.
  • the method of manufacturing a thin polarizing plate of the present invention after the step of separating the polyvinyl alcohol-based film and the base film with the protective film, the second side to the side where the protective film of the polyvinyl alcohol-based film is not attached
  • the method may further include attaching a protective film.
  • the adhesive layer on the surface where the protective film of the polyvinyl alcohol-based film is not attached may further comprise forming a.
  • the present invention is a polyvinyl alcohol polarizer having a thickness of 10 ⁇ m or less; And a first protective film attached to one surface of the polyvinyl alcohol-based polarizer, and has a single transmittance of 40% to 45% and a polarization degree of 99.0% or more.
  • the productivity is excellent, and a variety of forms of a polarizing plate in one process There is an advantage that can be prepared.
  • the thin polarizing plate manufactured according to the manufacturing method of the present invention is less curl, it is possible to minimize the light leakage phenomenon when applying the display device.
  • 1 is a schematic diagram showing a method for measuring adhesion using a texture analyzer (Texture Analyzer).
  • FIG. 2 is a view showing a state of a laminated film produced according to the method of Comparative Example 1.
  • Example 3 is a photograph showing curl characteristics of a thin polarizing plate manufactured by the method of Example, Comparative Example 3 and Comparative Example 4.
  • Figure 4 is a photograph showing the side portion curl phenomenon of the film laminate after stretching of Comparative Example 6.
  • FIG. 5 is a photograph showing a state of the film laminate after stretching in Example 2.
  • the inventors of the present inventors have conducted a long study to produce a polarizer having no optical breakage and excellent optical properties without breaking in the manufacturing process, and as a result, a polyvinyl alcohol-based film is attracted to the base film using an attractive force or an adhesive. It was found that the above object can be attained by drawing and attaching the same.
  • Korean Patent Application No. 10-2012-0130576 and Korean Patent Application No. 10-2012-0130577 There is a bar.
  • the inventors of the present invention through the further research, in the method for producing a thin polarizer, the step of attaching the first protective film on the polyvinyl alcohol-based film before the separation of the base film and the polyvinyl alcohol-based film.
  • the base film and the polyvinyl alcohol-based film are separated, the base film and the polyvinyl alcohol-based film are not only separated more cleanly, but also a polarizing plate having excellent curl characteristics can be produced, and the productivity can be further improved. It was found and completed the present invention.
  • the method of manufacturing a thin polarizing plate comprises the steps of: attaching a non-stretched polyvinyl alcohol-based film using a attraction force or an adhesive on an unstretched base film to form a film laminate; Stretching the film laminate; Attaching a first protective film on the polyvinyl alcohol-based film of the stretched film laminate; And separating the polyvinyl alcohol-based film and the base film to which the first protective film is attached.
  • an unstretched polyvinyl alcohol-based film is attached onto the unstretched base film by using attraction force or an adhesive to form a film laminate.
  • the unstretched polyvinyl alcohol-based film may be attached to one side or both sides of the unstretched base film.
  • a polyvinyl alcohol-based film is attached to both sides of the unstretched base film.
  • the unstretched base film is to prevent the polyvinyl alcohol-based film from breaking in the stretching process, preferably, may be a polymer film having a maximum draw ratio of 5 times or more under a temperature condition of 20 °C to 85 °C.
  • the maximum draw ratio means a draw ratio immediately before breakage occurs.
  • the stretching may be dry stretching or wet stretching, in the case of wet stretching, the stretching ratio in the case of stretching in an aqueous boric acid solution having a boric acid concentration of 1.0 to 5% by weight.
  • Such base films include, but are not limited to, high density polyethylene films, polyurethane films, polypropylene films, polyolefin films, ester films, low density polyethylene films, high density polyethylene and low density polyethylene coextrusion films, high density polyethylene Ethylene vinyl acetate-containing copolymer resin film, acrylic film, polyethylene terephthalate film, polyvinyl alcohol film, cellulose film and the like.
  • the base film used in the present invention may have a thickness of about 20 ⁇ m to 100 ⁇ m, preferably about 30 ⁇ m to 80 ⁇ m, and more preferably about 40 ⁇ m to 60 ⁇ m.
  • the thickness of the base film is less than 20 ⁇ m, breakage may occur due to insufficient support of the polyvinyl alcohol-based film in the stretching process of the film laminate, and when it exceeds 100 ⁇ m, the stretchability of the film laminate may be deteriorated. This is because it can prevent free width shrinkage during drying of the polyvinyl alcohol-based film, thereby inhibiting optical properties of the finally obtained polarizer.
  • the glass transition temperature of the base film is preferably lower than the glass transition temperature of the polyvinyl alcohol-based film, for example, it is preferably about 20 °C to 60 °C, preferably 30 °C to 60 °C.
  • the glass transition temperature of the polyvinyl alcohol-based film is about 70 ° C. to 80 ° C.
  • the base film is softer under the stretching temperature conditions. It can have a result, it is possible to stretch the polyvinyl alcohol-based film better.
  • the glass transition temperature of the base film is preferably 20 ° C.
  • the glass transition temperature may be measured by a differential scanning calorimeter (DSC).
  • DSC differential scanning calorimeter
  • the endothermic and calorific values generated by phase shifting are plotted according to the temperature. The temperature can be measured.
  • the base film may have a modulus at room temperature (25 ° C.) of about 200 MPa to 1500 MPa, preferably about 350 MPa to 1300 MPa.
  • a modulus at room temperature 25 ° C.
  • the modulus of the base film exceeds 1500MPa, high magnification stretching may be difficult, and when less than 200MPa, breakage may occur in the stretching process.
  • the modulus is fixed to both ends of the sample prepared according to JIS-K6251-1 standard, and then applied a force in a direction perpendicular to the thickness direction of the film to measure the stress per unit area according to the tensile rate (strain)
  • the value obtained by this is referred to, and a tensile force meter (Zwick / Roell Z010 UTM) etc. can be used as a measuring instrument.
  • the base film may have a force at break point at room temperature (25 ° C.) of about 5N to about 40N, preferably about 10N to about 30N.
  • the breaking force refers to a tensile force at the time when the base film is broken when the both ends of the film is fixed and a tensile force is applied in a direction perpendicular to the thickness direction of the film, for example, a tensile force meter (Zwick / Roell Z010 UTM) and the like can be measured.
  • a tensile force meter Zwick / Roell Z010 UTM
  • the unstretched polyvinyl alcohol-based film attached to the base film has a thickness of about 10 ⁇ m to 60 ⁇ m, preferably about 10 ⁇ m to 40 ⁇ m.
  • the thickness of the polyvinyl alcohol-based film exceeds 60 ⁇ m, it is difficult to achieve a thickness of 10 ⁇ m or less even when stretched, when the thickness is less than 10 ⁇ m tends to break during stretching.
  • the polyvinyl alcohol-based film is not limited to this, but the degree of polymerization is preferably about 1,000 to 10,000, preferably 1,500 to 5,000. This is because when the degree of polymerization satisfies the above range, the molecular motion is free and can be mixed flexibly with iodine or dichroic dye.
  • polyvinyl alcohol-based film of the present invention a commercially available polyvinyl alcohol-based film may be used.
  • PS30, PE30, PE60 manufactured by Gurere, M2000, M3000 M6000, etc. may be used.
  • the base film and the polyvinyl alcohol-based film is attached by a weak attraction force generated on the surface of the base film and the unstretched polyvinyl alcohol-based film without a separate medium, or may be attached via an adhesive Can be.
  • the base film and the unstretched polyvinyl alcohol-based film may be treated by surface treatment on one or both surfaces of the base film or the polyvinyl alcohol-based film.
  • the surface treatment may be performed through various surface treatment methods well known in the art, for example, corona treatment, plasma treatment, or surface modification treatment using a strong base aqueous solution such as NaOH or KOH.
  • the thickness of the adhesive layer before stretching may be about 20 nm to 4000 nm, preferably about 20 nm to 1000 nm, and more preferably about 20 nm to 500 nm.
  • the thickness of the adhesive layer after the stretching of the film laminate may be about 10nm to 1000nm, preferably 10nm to 500nm, more preferably 10nm to 200nm.
  • the adhesive the material is not particularly limited, various adhesives known in the art can be used without limitation.
  • the adhesive layer may be formed of an aqueous adhesive or an ultraviolet curable adhesive.
  • the aqueous adhesive preferably includes an amine metal compound crosslinking agent in an acetacetyl group-containing polyvinyl alcohol-based resin. More specifically, the adhesive may be an aqueous solution containing 100 parts by weight of a polyvinyl alcohol-based resin containing an acetacetyl group and 1 to 50 parts by weight of an amine metal compound crosslinking agent.
  • the polymerization degree and saponification degree of the polyvinyl alcohol-based resin are not particularly limited as long as they contain acetacetyl group, but the polymerization degree is 200 to 4,000, and the saponification degree is preferably 70 mol% to 99.9 mol%.
  • the degree of polymerization is 1,500 to 2,500, and the degree of saponification is more preferably 90 mol% to 99.9 mol%.
  • the polyvinyl alcohol-based resin preferably comprises 0.1 to 30 mol% of the acetacetyl group.
  • the reaction with the amine-based metal compound crosslinking agent may be smooth, and may be sufficiently significant for the water resistance of the desired adhesive.
  • the amine-based metal compound crosslinking agent is a water-soluble crosslinking agent having a functional group having reactivity with the polyvinyl alcohol-based resin, preferably in the form of a metal complex containing an amine ligand.
  • Possible metals include zirconium (Zr), titanium (Ti), hafnium (Hf), tungsten (W), iron (Fe), cobalt (Co), nickel (Ni), ruthenium (Ru), osmium (Os), Transition metals such as rhodium (Rh), iridium (Ir), palladium (Pd) and platinum (Pt) are possible, and ligands bound to the central metal are primary amines, secondary amines (diamines), tertiary amines or ammonium hydrides. As long as it contains at least 1 or more amine groups, such as a lockside, it is all possible.
  • the solid content of the polyvinyl alcohol-based resin containing the acetacetyl group is preferably about 1% by weight to about 10% by weight. If the solid content of the polyvinyl alcohol-based resin is less than 1% by weight, the water resistance is not sufficiently secured, so that the effect of lowering the breakage rate in the stretching process is less. If the content is more than 10% by weight, the workability is deteriorated. This is because damage may occur on the alcohol-based film surface.
  • the pH of the adhesive is preferably 4.5 to 9 or so.
  • fills the said numerical range it is because it is more advantageous in storage property and durability in a high humidity environment.
  • the pH of the adhesive can be adjusted by the method of containing an acid in the aqueous solution, wherein the acid used for pH adjustment can be used both strong and weak acid.
  • the acid used for pH adjustment can be used both strong and weak acid.
  • nitric acid, hydrochloric acid, sulfuric acid or acetic acid and the like can be used.
  • the thickness of the adhesive layer formed by the above adhesive is about 80 nm to 200 nm, preferably about 80 nm to 150 nm before stretching the film laminate, and after stretching the film laminate, about 10 nm to 100 nm, preferably 10 nm to It is preferable that it is about 80 nm.
  • the thickness of the adhesive layer satisfies the above range, the adhesive force between the polyurethane film and the polyvinyl alcohol-based film is maintained at an appropriate level, so that the breakage rate in the stretching process is lowered and the polarizer surface damage during peeling can be minimized. to be.
  • the said adhesive agent In the case of the said adhesive agent, a crosslinking reaction occurs between the amine type metal compound and the acetacetyl group of polyvinyl alcohol-type resin at the time of hardening, and the water resistance of the adhesive layer after hardening becomes very excellent. Therefore, when the polymer film and the polyvinyl alcohol-based film are laminated using the adhesive, the phenomenon in which the adhesive dissolves in water during wet stretching can be minimized, and thus it can be particularly useful when performing wet stretching. .
  • the adhesive layer may be formed of an ultraviolet curable adhesive, for example, a first epoxy compound having a glass transition temperature of homopolymer of 120 ° C. or more, a second epoxy compound having a glass transition temperature of homopolymer of 60 ° C. or less and It may be formed of an ultraviolet curable adhesive containing a cationic photopolymerization initiator.
  • the UV-curable adhesive is 100 parts by weight of the first epoxy compound having a glass transition temperature of the homopolymer of 120 °C or more, 30 to 100 parts by weight of the second epoxy compound having a glass transition temperature of the homopolymer of 60 °C or less and cationic photopolymerization It may include 0.5 to 20 parts by weight of the initiator.
  • an epoxy compound refers to a compound having one or more epoxy groups in a molecule, preferably a compound having two or more epoxy groups in a molecule, and is in the form of a monomer, a polymer, or a resin.
  • the concept includes all of the compounds.
  • the epoxy compound of the present invention may be in the form of a resin.
  • the glass transition temperature of the homopolymer is an epoxy compound of 120 °C or more can be used without particular limitation, for example, the alicyclic epoxy compound and the glass transition temperature of the homo polymer is 120 °C or more and / Or aromatic epoxy may be used as the first epoxy compound of the present invention.
  • Specific examples of the epoxy compound having a glass transition temperature of homopolymer of 120 ° C or higher include 3,4-epoxycyclohexylmethyl-3,4'-epoxycyclohexanecarboxylate, vinylcyclohexenedioxide dicyclopentadiene dioxide, and bisepoxycyclo.
  • the first epoxy compound is more preferably the glass transition temperature of the homopolymer is about 120 °C to 200 °C.
  • the second epoxy compound may be used without particular limitation as long as the glass transition temperature of the homopolymer is an epoxy compound of 60 ° C. or less.
  • an alicyclic epoxy compound, an aliphatic epoxy compound, or the like may be used as the second epoxy compound.
  • alicyclic epoxy compound it is preferable to use a bifunctional epoxy compound, that is, a compound having two epoxies, and more preferably use a compound in which the two epoxy groups are both alicyclic epoxy groups. It is not limited.
  • the epoxy compound which has an aliphatic epoxy group which is not an alicyclic epoxy group can be illustrated.
  • polyglycidyl ether of aliphatic polyhydric alcohol Polyglycidyl ethers of alkylene oxide adducts of aliphatic polyhydric alcohols; Polyglycidyl ethers of polyester polyols of aliphatic polyhydric alcohols and aliphatic polyhydric carboxylic acids; Polyglycidyl ethers of aliphatic polyvalent carboxylic acids; Polyglycidyl ethers of polyester polycarboxylic acids of aliphatic polyhydric alcohols and aliphatic polyhydric carboxylic acids; Dimers, oligomers or polymers obtained by vinyl polymerization of glycidyl acrylate or glycidyl methacrylate; Or oligomers or polymers obtained by vinyl polymerization of glycidyl acrylate or glycidyl me
  • aliphatic polyhydric alcohol for example, an aliphatic polyhydric alcohol having 2 to 20 carbon atoms, 2 to 16 carbon atoms, 2 to 12 carbon atoms, 2 to 8 carbon atoms or 2 to 4 carbon atoms may be exemplified.
  • Ethylene glycol 1,2-propanediol, 1,3-propanediol, 2-methyl-1,3-propanediol, 2-butyl-2-ethyl-1,3-propanediol, 1,4-butanediol, neo Pentyl glycol, 3-methyl-2,4-pentanediol, 2,4-pentanediol, 1,5-pentanediol, 3-methyl-1,5-pentanediol, 2-methyl-2,4-pentanediol, 2,4-diethyl-1,5-pentanediol, 1,6-hexanediol, 1,7-heptanediol, 3,5-heptanediol, 1,8-octanediol, 2-methyl-1,8- Aliphatic diols such as octanediol, 1,9-nonane
  • alkylene oxide of 1 to 20 carbon atoms, 1 to 16 carbon atoms, 1 to 12 carbon atoms, 1 to 8 carbon atoms or 1 to 4 carbon atoms can be exemplified, for example, ethylene jade Seeds, propylene oxide or butylene oxide and the like can be used.
  • aliphatic polyhydric carboxylic acid For example, oxalic acid, malonic acid, succinic acid, glutaric acid, adipic acid, pimelic acid, sumeric acid, azelaic acid, sebacic acid, dodecane diacid, 2-methyl succinic acid, 2-methyladipic acid, 3-methyladipic acid, 3-methylpentaneic acid, 2-methyloctanoic acid, 3,8-dimethyldecanediic acid, 3,7-dimethyldecanediic acid, 1,20-eicosamethylenedica Carboxylic acid, 1,2-cyclopentanedicarboxylic acid, 1,3-cyclopentanedicarboxylic acid, 1,2-cyclohexanedicarboxylic acid, 1,3-cyclohexanedicarboxylic acid, 1, 4-cyclohexanedicarboxylic acid, 1,4-dicarboxymethylenecyclohexane, 1,2,3-propylic acid, 1,
  • the second epoxy compound of the present invention may include one or more glycidyl ether groups, for example, 1,4-cyclohexanedimethanol diglycidyl ether, 1,4-butanediol diggle Cydyl ether, 1,6-hexanediol diglycidyl ether, neopentyl diglycidyl ether, resorcinol diglycidyl ether, diethylene glycol diglycidyl ether, ethylene glycol diglycidyl ether, One selected from the group consisting of trimethylolpropanetriglycidyl ether, n-butyl glycidyl ether, 2-ethylhexyl glycidyl ether, phenyl glycidyl ether, and o-cresyl glycidyl ether The above can be used as the second epoxy compound of the present invention.
  • the second epoxy compound has a glass transition temperature of about 0 ° C to 60 ° C of the homopolymer.
  • the present invention is not limited thereto, but in the present invention, it is preferable to use a combination of the first epoxy compound including at least one epoxidized aliphatic ring group and the second epoxy compound including at least one glycidyl ether group as the epoxy compound. Particularly preferred.
  • the stretching is preferably carried out so that the thickness of the polyvinyl alcohol-based film is less than 10 ⁇ m, for example, the thickness of the polyvinyl alcohol-based film is 1 ⁇ m to 10 ⁇ m, 3 ⁇ m to 10 ⁇ m or 1 ⁇ m It is preferable to carry out so that it becomes about 5 micrometers.
  • the stretching is preferably performed so that the width shrinkage of the polyvinyl alcohol-based film is about 30% to 80%, preferably about 60% to 80%. This is because when the width shrinkage ratio of the polyvinyl alcohol-based film satisfies the numerical range, excellent optical properties can be obtained.
  • the stretching conditions are not particularly limited, for example, the stretching may be carried out at a draw ratio of 5 times to 15 times at a temperature of 20 °C to 85 °C, more preferably 40 It may be carried out at a draw ratio of 5 to 12 times at a temperature of °C to 80 °C.
  • the stretching may be performed by wet stretching or dry stretching.
  • wet stretching since the surface adhesion of the base film and the polyvinyl alcohol-based film is stronger than the dry stretching, the stretching can be performed stably without a separate bonding means.
  • the wet stretching is preferably carried out in an aqueous boric acid solution, wherein the boric acid concentration of the aqueous boric acid solution is preferably about 1.0 to 5.0 wt%.
  • the manufacturing process of the polarizing element is a process of washing with water, swelling, dyeing, washing, stretching, complementary color, drying and the like
  • the washing and stretching process is preferably carried out in an aqueous boric acid solution.
  • the boric acid concentration may be about 0.1 to 2.5 wt%, preferably about 0.5 to 2.0 wt%
  • the boric acid concentration is about 1.0 to 5.0 wt%, preferably 1.5 to It may be about 4.5 wt%.
  • the stretching step at least one of the step of dyeing iodine and / or dichroic dye on the polyvinyl alcohol-based film and / or cross-linking the dyed iodine and / or dichroic dye to the polyvinyl alcohol-based film It may be performed together with the above steps.
  • the dyeing, crosslinking and stretching processes can be performed simultaneously.
  • the film laminate with the dyeing completed is immersed in an aqueous solution of boric acid, and stretched in an aqueous solution of boric acid.
  • the crosslinking step and the stretching step may be performed together.
  • the adhesion between the stretched polyvinyl alcohol-based film and the stretched base film after the stretching of the film laminate is 2N / 2cm or less, preferably, about 0.1 to 2N / 2cm, more preferably about 0.1 to 1N / 2cm.
  • the adhesion between the stretched base film and the stretched polyvinyl alcohol film satisfies the above range, surface damage can be minimized during the separation process.
  • the adhesive layer is formed between the polyvinyl alcohol-based film and the base film, not only the polyvinyl alcohol-based film and the base film but also the adhesive layer are stretched together.
  • the thickness is reduced to a level of 10 to 50% compared to before stretching, and as a result, the adhesion force between the polyvinyl alcohol-based film and the base film is lowered to 2N / 2 cm or less, thereby making it easy to separate.
  • the adhesive force is the adhesive force measured when the sample films of 2cm length is attached, a specific measuring method is shown in FIG.
  • the adhesion between the films as shown in Figure 1, after fixing the polyvinyl alcohol film (A) of the film laminate with a sample holder (H), with respect to the surface direction of the film laminate Peel strength measured by peeling the polyvinyl alcohol film (A) from the base film (B) by applying a force in a vertical direction, wherein the measuring instrument is a texture analyzer (Stable Micro Systems, Inc.) TA-XT Plus) was used.
  • the drying is preferably 20 to 100 °C, more preferably about 40 to 90 °C, it is preferably carried out for 1 to 10 minutes at the above temperature.
  • the drying process prevents the PVA polarizer from deteriorating the physical properties of the PVA polarizer by water removal in the PVA surface and water by removing moisture from the PVA, and induces the width shrinkage of the polyvinyl alcohol film stretched during the drying process. It serves to improve the polarization degree of the polarizer by increasing the orientation of the complex composed of iodine.
  • the first protective film is attached onto the polyvinyl alcohol-based film of the stretched film laminate.
  • a polyvinyl alcohol film is affixed on both surfaces of a base film, a 1st protective film can be affixed on each polyvinyl alcohol-type film.
  • various films used in the art as a polarizer protective film or a retardation film, and a film for improving brightness may be used without limitation, for example, a polyester polymer, a styrene polymer, Cellulose polymer, polyether sulfone polymer, polycarbonate polymer, acrylic polymer, polyolefin polymer, polyamide polymer, polyimide polymer, sulfone polymer, polyether sulfone polymer, polyether ether ketone polymer, poly At least one selected from the group consisting of phenylene sulfide polymers, vinyl alcohol polymers, vinylidene chloride polymers, vinyl butyral polymers, arylate polymers, polyoxy methylene polymers, epoxy polymers and mixtures of these polymers This can be used.
  • the 1st protective film attached to each polyvinyl alcohol-type film may be the same and may differ.
  • a polarizing plate including different protective films can be manufactured in one process.
  • the attachment of the first protective film may be performed using an adhesive, and in this case, the adhesive may be used using an adhesive or pressure-sensitive adhesive for a polarizing plate well known in the art.
  • the pressure-sensitive adhesive or adhesive may be appropriately selected in consideration of the material of the first protective film to be used, for example, in the case of using a cellulose-based film as the first protective film, such as a polyvinyl alcohol-based adhesive An adhesive can be used, and when an acrylic film, a cycloolefin film, etc. are used for a 1st protective film, the photocuring or thermosetting adhesives, such as an acrylic adhesive and an epoxy adhesive, can be used.
  • the polyvinyl alcohol-based film and the base film to which the first protective film is attached are separated.
  • the separating step may be performed by applying a weak peeling force to the polyvinyl alcohol-based film or the base film to which the first protective film is attached, thereby leaving both films.
  • the peel force is preferably 2N / 2cm or less, for example, may be 0.1 to 2N / 2cm, 0.1 to 1N / 2cm or so.
  • the adhesion between the base film and the polyvinyl alcohol-based film is low, and the adhesive force between the first protective film and the polyvinyl alcohol-based film is relatively high compared to the adhesion between the polyvinyl alcohol-based film and the base film
  • a weak peel force is applied, the polyvinyl alcohol-based film and the base film are cleanly separated.
  • the peeling force required to separate the polyvinyl alcohol-based film and the polymer film is very weak compared to the case of lamination using a coating or co-extrusion, the two films can be easily separated without any other process or equipment. In the separation process, the damage of the polyvinyl alcohol-based film is small and shows very good optical performance.
  • a polarizing plate having a first protective film attached to one surface of a polyvinyl alcohol-based film having a thickness of 10 ⁇ m or less is obtained.
  • a polyvinyl alcohol-type film is affixed on both surfaces of a base film, two polarizing plates can be obtained by one process.
  • the thin polarizing plate having the first protective film attached to one surface thus obtained has a step of forming an adhesive layer on the surface on which the first protective film of the polyvinyl alcohol-based film is not attached and / or the first protective film of the polyvinyl alcohol-based film. Attaching the second protective film to this unattached surface may be further performed.
  • the adhesive layer forming step the adhesive layer is one selected from the group consisting of acrylic copolymer, epoxy resin, polyurethane resin, silicone resin, polyether resin, polyamide resin and polyvinyl alcohol resin.
  • the pressure-sensitive adhesive composition may be applied to a surface on which the first protective film of the polyvinyl alcohol-based film is not attached, and then cured by irradiation with light or heat.
  • the second protective film attaching step may be performed by using an adhesive, and in this case, the adhesive may be performed using an adhesive or an adhesive for a polarizing plate well known in the art.
  • the pressure-sensitive adhesive or adhesive may be appropriately selected in consideration of the material of the first protective film to be used, for example, in the case of using a cellulose-based film as the second protective film, such as a polyvinyl alcohol-based adhesive An adhesive can be used, and when an acrylic film, a cycloolefin film, etc. are used as a 2nd protective film, the photocuring or thermosetting adhesives, such as an acrylic adhesive and an epoxy adhesive, can be used.
  • various films used in the art as a polarizer protective film or a retardation film can be used without limitation, for example, polyester polymer, styrene polymer, cellulose polymer, poly Ether sulfone type polymer, polycarbonate type polymer, acrylic type polymer, polyolefin type polymer, polyamide type polymer, polyimide type polymer, sulfone type polymer, poly ether sulfone type polymer, polyether ether ketone type polymer, polyphenylene sulfide type It is preferably made of one or more selected from the group consisting of polymers, vinyl alcohol polymers, vinylidene chloride polymers, vinyl butyral polymers, arylate polymers, polyoxy methylene polymers, epoxy polymers and mixtures of these polymers. Do.
  • a single-sided polarizing plate including the protective film may be produced on only one surface of the polyvinyl alcohol-based film.
  • a double-sided polarizing plate can be produced, there is an advantage that a polarizing plate of various kinds can be produced through the manufacturing method of the present invention.
  • the sheet-to-sheet process is a method using a sheet-like film cut to a predetermined size with a raw film (ie, polyvinyl alcohol-based film, base film, protective film, etc.), the sheet-to-roll process As a raw material film, the roll type film by which the long film was wound is used, and the other raw material film says the method of using the sheet
  • a roll-to-roll process is a method of using a rolled film as a raw film. In view of the continuity and productivity of the process, it is particularly preferred to use a roll-to-roll process among these.
  • the base film and the polyvinyl alcohol-based film have an adhesion force of 2 N / 2 cm or less while unwinding the polyvinyl alcohol-based film and the base film from the base film roll and the polyvinyl alcohol-based film roll.
  • the base film and the polyvinyl alcohol-based film is attached, and then re-wound in a roll shape, then unwind the film laminate from the re-wound film laminate roll may be introduced into the stretching process, or without rewinding It can be directly put into the stretching process.
  • a peeling means for example, a peeling roll
  • a peeling roll is inserted between the base film and the polyvinyl alcohol-based film to separate the interface between the base film and the polyvinyl alcohol-based film, and then separated from the base film. It can be carried out by a method of winding the polyvinyl alcohol-based film in a roll with each other.
  • the polarizing plate of the present invention prepared by the above method has a thickness of 10 ⁇ m or less, for example, 1 ⁇ m to 10 ⁇ m, 3 ⁇ m to 10 ⁇ m, or 1 ⁇ m to 5 ⁇ m polyvinyl alcohol polarizer; And a first protective film attached to one surface of the polyvinyl alcohol polarizer, and, if necessary, further include an adhesive layer and / or a second protective film on an opposite surface of the surface on which the first protective film is attached. Can be.
  • the unitary transmittance is about 40 to 45%, and the polarization degree is 99.0% or more, 99.5% or more, more preferably 99.7% or more, and is excellent in optical characteristics.
  • the polarizing plate of this invention is excellent also in the uniformity of the polarization degree to the width direction.
  • the standard deviation of the degree of polarization measured at ten points positioned at equal intervals along the width direction of the polarizing plate is 0.002% or less.
  • the polarizing plate of the present invention hardly generates curl, and has excellent flatness. More specifically, when the polarizing plate of the present invention is placed on a flat surface, the distance between the four corners of the polarizing plate and the bottom surface is measured, and the arithmetic mean value of the measured values is obtained, the value is very flat to 5 mm or less.
  • the polarizing plate of the present invention in addition to the first protective film, the second protective film or the adhesive layer may further include other functional optical layer, such as brightness enhancement film, primer layer, hard coating layer, anti-glare layer or anti-reflection layer. have.
  • the formation method of these optical layers is not specifically limited, The well-known method well known in the art can be used.
  • the polarizing plate of the present invention has a very thin thickness compared to the conventional polarizing plate and has excellent optical properties, and thus may be usefully used in display devices such as liquid crystal display panels and organic light emitting display devices.
  • a laminate was formed, and a thin polarizer manufacturing experiment was conducted through a wet stretching process.
  • the PVA film M3000 grade 30 ⁇ m PVA was used.
  • the PVA film was subjected to a swelling process in a 25 ° C. pure solution for 15 seconds, followed by a dyeing process for 60 seconds in a 0.3 wt% concentration and a 25 ° C. iodine solution. Thereafter, after washing for 15 seconds in a solution of 1 wt% boric acid and 25 ° C., a 7-fold stretching process was performed in a solution of 2.5 wt% boric acid and 52 ° C.
  • the process was complementary in a 5 wt% KI solution, followed by drying in an 80 ° C. oven for 5 minutes. After drying, the thickness of the PVA film was about 6-8 micrometers.
  • 40 ⁇ m triacetyl cellulose (TAC) film was placed on each side of the PVA polarizer attached to both sides of the substrate, laminated with a laminator through a PVA-based water-soluble adhesive, and dried in an 80 ° C. oven for 5 minutes. Thereafter, the PVA polarizer having the TAC laminated on one side was peeled off from both sides of the substrate to secure the PVA polarizer having the TAC attached to one side.
  • TAC triacetyl cellulose
  • TAC triacetyl cellulose
  • PVA film (M-grade, Nippon Synthetic Co., Ltd., average polymerization degree: 2400 average saponification degree: 99mol%) was dissolved in 100 ° C pure water to form a PVA aqueous solution, and then a lip coater was placed on a 200 ⁇ m-thick PET (NOVA-Clear SG007 grade of MCC). It was coated using and dried for 10 minutes in an oven at 80 °C to form a laminated film. At this time, the thickness of the said PVA film was 10 micrometers. The laminated film was subjected to a swelling process for 15 seconds in a 25 ° C. pure solution, followed by a dyeing process for 60 seconds in a 0.3 wt% concentration and a 25 ° C.
  • PVA film (M-grade, Nippon Synthetic Co., Ltd., average polymerization degree: 2400 average saponification degree: 99mol%) was dissolved in 100 ° C pure water to form a PVA aqueous solution, and then a lip coater was placed on a 200 ⁇ m-thick PET (NOVA-Clear SG007 grade of MCC). It was coated using and dried for 10 minutes in an oven at 80 °C to form a laminated film. At this time, the thickness of the said PVA film was 10 micrometers. The laminated film was subjected to a swelling process in a 1.0 wt% aqueous solution of boric acid at 25 ° C.
  • TAC triacetyl cellulose
  • TAC triacetyl cellulose
  • Japan Synthetic Co., Ltd. M3000 grade 30 ⁇ m PVA film used in the Example was stretched alone 6 times under the same stretching conditions as the process conditions of Example to finally prepare a polarizing device having a thickness of 13 ⁇ m.
  • a 40 ⁇ m triacetyl cellulose (TAC) film was placed on both sides of the polarizer, and laminated with a laminator through a PVA-based water-soluble adhesive, followed by drying in an oven at 80 ° C. for 5 minutes to prepare a polarizing plate having a TAC / PVA / TAC structure. .
  • Nippon Synthetic M6000 grade 60 ⁇ m PVA film used in the examples was stretched alone 6 times under the same stretching conditions as in the process conditions of the example to finally prepare a general polarizer having a thickness of 22 ⁇ m.
  • a 40 ⁇ m triacetyl cellulose (TAC) film was placed on both sides of the polarizer, and laminated with a laminator through a PVA-based water-soluble adhesive, followed by drying in an oven at 80 ° C. for 5 minutes to prepare a polarizing plate having a TAC / PVA / TAC structure. .
  • the polarization degree was measured at ten points located at equal intervals along the width direction of the polarizer, and then the standard deviation value of the measured polarization degree was calculated.
  • Polarization degree was measured by JASCO V-7100 Spectrophotometer. The measurement results are shown in the following [Table 2].
  • a 4% by weight aqueous solution was prepared by dissolving polyvinyl alcohol (average degree of polymerization 2000, degree of 94%, Japanese Synthetic) containing acetacetyl group (5% by weight) in pure water. Titanium amine complex crosslinking agent (product name: TYZOR TE, DuPont) was added in a ratio of 6.7 parts by weight per 100 parts by weight of polyvinyl alcohol and mixed with stirring to prepare an adhesive A.
  • polyvinyl alcohol average degree of polymerization 2000, degree of 94%, Japanese Synthetic
  • Titanium amine complex crosslinking agent product name: TYZOR TE, DuPont
  • M2000 grade 20 ⁇ m PVA film manufactured by Nippon Synthetic Fiber was laminated and passed through a laminator to form a film laminate.
  • the prepared film laminate was swelled in a 25 ° C. pure solution for 15 seconds and then dyed for 60 seconds in a 0.3 wt% concentration and 25 ° C. iodine solution. Thereafter, after washing for 15 seconds in a solution of 1 wt% boric acid and 25 ° C., a 7-fold stretching process was performed in a solution of 2.5 wt% boric acid and 52 ° C.
  • the process was complementary in a 5 wt% KI solution, followed by drying in an 80 ° C. oven for 5 minutes. After drying, the thickness of the PVA film was about 7.5 ⁇ m.
  • 40 ⁇ m triacetyl cellulose (TAC) film was placed on each side of the PVA polarizer attached to both sides of the substrate, laminated with a laminator through a PVA-based water-soluble adhesive, and dried in an 80 ° C. oven for 5 minutes. Thereafter, the PVA polarizer with TAC laminated on one side was peeled off from both sides of the base film with a peel force of 0.7 N / 2 cm to obtain a PVA polarizer with TAC attached to one side.
  • TAC triacetyl cellulose
  • the PVA film was laminated and passed through a laminator to form a film laminate.
  • the prepared film laminate was swelled in a 25 ° C. pure solution for 15 seconds and then dyed for 60 seconds in a 0.3 wt% concentration and 25 ° C. iodine solution. Thereafter, after washing for 15 seconds in a solution of 1 wt% boric acid and 25 ° C., a stretching process was performed 7 times in a solution of 2.5 wt% boric acid and 52 ° C., but breakage occurred during stretching.
  • a polyvinyl alcohol-based adhesive (trade name: JC25, manufacturer: JAPAN VAM & POVAL Co., Ltd.) of commercially available solid content of 4 wt% on both sides of a 40 ⁇ m-thick thermoplastic polyurethane substrate, M2000 grade 20 ⁇ m of Japan Synthetic
  • the PVA film was laminated and passed through a laminator to form a film laminate.
  • the prepared film laminate was swelled in a 25 ° C. pure solution for 15 seconds and then dyed for 60 seconds in a 0.3 wt% concentration and 25 ° C. iodine solution.
  • FIG. 4 is a photograph showing the state of the film laminate after stretching of Comparative Example 6.
  • Figure 5 is a photograph showing the state of the film laminate after stretching of Example 2. As shown in FIGS. 4 and 5, the film laminate of Comparative Example 6 had side curl after stretching, whereas this phenomenon did not occur in the film laminate of Example 2.
  • FIG. 4 and 5 the film laminate of Comparative Example 6 had side curl after stretching, whereas this phenomenon did not occur in the film laminate of Example 2.

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  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Optics & Photonics (AREA)
  • Polarising Elements (AREA)
  • Laminated Bodies (AREA)

Abstract

La présente invention concerne un procédé de fabrication d'une plaque polarisante mince, comportant les étapes consistant à: fixer un film non étiré à base de polyalcool de vinyle sur un film non étiré en matériau de base au moyen d'une force d'attraction ou d'un adhésif pour former ainsi un corps feuilleté en film; étirer le corps feuilleté en film; fixer un premier film protecteur au film à base de polyalcool de vinyle du corps feuilleté étiré en film; et séparer un film de base et le film à base de polyalcool de vinyle auquel est fixé le premier film protecteur.
PCT/KR2014/005188 2013-06-18 2014-06-13 Plaque polarisante mince et procédé pour sa fabrication WO2014204134A1 (fr)

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US14/385,727 US10048417B2 (en) 2013-06-18 2014-06-13 Thin polarizing plate and method of manufacturing the same
JP2015523044A JP6173451B2 (ja) 2013-06-18 2014-06-13 薄型偏光板及びその製造方法

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CN107664788A (zh) * 2016-07-29 2018-02-06 住友化学株式会社 光学层叠体
WO2018062642A1 (fr) * 2016-09-30 2018-04-05 삼성에스디아이 주식회사 Plaque polarisante et dispositif d'affichage optique la comprenant
CN108957840A (zh) * 2018-08-21 2018-12-07 京东方科技集团股份有限公司 一种显示模组、显示装置、偏光片及其制备方法

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CN111500209A (zh) * 2020-06-09 2020-08-07 京东方科技集团股份有限公司 可分离保护膜及其剥离方法、显示面板和电子设备

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