CN100381839C - polarizing board and its mfg. method - Google Patents
polarizing board and its mfg. method Download PDFInfo
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- CN100381839C CN100381839C CNB2004100451591A CN200410045159A CN100381839C CN 100381839 C CN100381839 C CN 100381839C CN B2004100451591 A CNB2004100451591 A CN B2004100451591A CN 200410045159 A CN200410045159 A CN 200410045159A CN 100381839 C CN100381839 C CN 100381839C
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- polyvinyl alcohol
- diaphragm
- cementing agent
- resin
- polarizer
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F17—STORING OR DISTRIBUTING GASES OR LIQUIDS
- F17C—VESSELS FOR CONTAINING OR STORING COMPRESSED, LIQUEFIED OR SOLIDIFIED GASES; FIXED-CAPACITY GAS-HOLDERS; FILLING VESSELS WITH, OR DISCHARGING FROM VESSELS, COMPRESSED, LIQUEFIED, OR SOLIDIFIED GASES
- F17C13/00—Details of vessels or of the filling or discharging of vessels
- F17C13/12—Arrangements or mounting of devices for preventing or minimising the effect of explosion ; Other safety measures
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F17—STORING OR DISTRIBUTING GASES OR LIQUIDS
- F17C—VESSELS FOR CONTAINING OR STORING COMPRESSED, LIQUEFIED OR SOLIDIFIED GASES; FIXED-CAPACITY GAS-HOLDERS; FILLING VESSELS WITH, OR DISCHARGING FROM VESSELS, COMPRESSED, LIQUEFIED, OR SOLIDIFIED GASES
- F17C2260/00—Purposes of gas storage and gas handling
- F17C2260/04—Reducing risks and environmental impact
- F17C2260/042—Reducing risk of explosion
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- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- General Engineering & Computer Science (AREA)
- Polarising Elements (AREA)
- Laminated Bodies (AREA)
Abstract
To increase the adhesion strength between a protective film and a polarizing film in the process of laminating a protective film made of a cycloolefin resin on a polyvinyl alcohol-based polarizing film to produce a polarizing plate. The polarizing plate is produced by laminating a protective film made of cycloolefin resin on one or both of the surfaces of a polyvinyl alcohol polarizing film via an adhesive layer. The adhesive layer contains a urethane adhesive and polyvinyl alcohol resin. The polyvinyl alcohol-based resin is a saponification product of a copolymer of vinyl acetate and monomers copolymerizable with the vinyl acetate. In the processes of manufacturing the polarizing plate, a urethane adhesive and an aqueous solution of polyvinyl alcohol-based resin which is a saponification product of a copolymer of vinyl acetate and other monomers copolymerizable with the vinyl acetate are mixed to prepare the adhesive. Preferably, the adhesive is applied to the surface of the polarizing film or the protective film within 5 minutes after mixing, and subjected to the process of laminating both films.
Description
Technical field
The present invention relates at the one side upper strata voltage protection film at least of light polarizing film and the Polarizer and the manufacture method thereof that form.
Background technology
As light polarizing film, adopt on the polyvinyl alcohol resin film absorption bitintability pigment in the prior art always and make its orientation and the film that forms.Known to the iodine polarizing film of iodine as the bitintability pigment, and be light polarizing film with the bitintability dyestuff as the dyestuff of bitintability pigment.These light polarizing film normally on its at least one surface, the diaphragm of cementing agent applying triacetyl cellulose that preferably aqueous solution by polyvinyl alcohol resin forms on two surfaces etc., make Polarizer thus.But when the Polarizer of Gou Chenging used under wet heat condition for a long time thus, the problem of generation was that polarizing properties reduces easily, and the end face of diaphragm and light polarizing film is also peeled off easily.
At these problems, proposed to adopt the scheme of thermoplasticity cyclic olefine resin as the diaphragm use of Polarizer.For example opening in the flat 5-212828 communique (patent documentation 1) the spy, disclose at least one surface of polyethenol series thin slice, is resin flake by acrylic acid series cementing agent lamination thermoplasticity saturated norbornene, and carries out hot pressing and the Polarizer that forms.In addition; open in the 2000-321430 communique (patent documentation 2) the spy; disclose at least one surface of polyethenol series light polarizing film; by the adhesive layer of polyethenol series cementing agent and dual liquid type binder mixtures, the diaphragm that lamination is formed by annular ethylene series resin and the Polarizer that forms.In addition, open the spy that to disclose in the 2000-321432 communique (patent documentation 3) polyethenol series light polarizing film and thermoplasticity saturated norbornene be that diaphragm that resin forms adopts the polyurethane series cementing agent to bond and the Polarizer that forms.
But himself thickness of the cementing agent of acrylic acid series etc. (being called as the pressure-sensitive cementing agent) is 10-50 μ m, and some thickness can not obtain.In addition, when the cementing agent of general known employing polyethenol series and carbamate system, acrylic acid series, vinyl acetate system etc. bonds polyethenol series light polarizing film and cyclic olefine resin molding, two films are made up, and cohesiveness is not necessarily enough thus.
On the other hand, mainly triacetyl cellulose etc. is used as diaphragm in the prior art, therefore the bonding for itself and polyethenol series light polarizing film has also proposed various schemes always.For example, open in the flat 8-101307 communique (patent documentation 4), put down in writing polyethenol series light polarizing film and support (diaphragm) and carried out the Polarizer that lamination forms by the cementing agent that the pure and mild aliphatics polyvalent isocyanate of polyester polyols forms the spy.In addition, the spy opens in the flat 9-258023 communique (patent documentation 5), has put down in writing at least one surface of polyethenol series light polarizing film, is fitted with the Polarizer of diaphragm by the polyethenol series cementing agent that contains the soluble epoxide compound.
Patent documentation 1: the spy opens flat 5-212828 communique
Patent documentation 2: the spy opens the 2000-321430 communique
Patent documentation 3: the spy opens the 2000-321432 communique
Patent documentation 4: the spy opens flat 8-101307 communique
Patent documentation 5 spies open flat 9-258023 communique
Summary of the invention
The objective of the invention is the diaphragm that on polyethenol series light polarizing film lamination forms by the cyclic olefine resin and when forming Polarizer, adopt suitable cementing agent to improve the cohesive force of the two.
Present inventors etc. have carried out wholwe-hearted research at this purpose; found that; during lamination is formed by the cyclic olefine resin on the polyethenol series light polarizing film diaphragm; adopting carbamate is that the potpourri of polyvinyl alcohol resin of cementing agent and specific composition is as cementing agent; can obtain the Polarizer of the cohesiveness excellence of light polarizing film and diaphragm, reach purpose of the present invention thus.
Promptly; according to the invention provides such Polarizer; it is to pass through adhesive layer; the diaphragm that lamination is formed by the cyclic olefine resin on surface of polyethenol series light polarizing film or two surfaces and the Polarizer that forms; it is cementing agent and polyvinyl alcohol resin that adhesive layer contains carbamate, this polyvinyl alcohol resin be vinyl acetate and can be with the multipolymer of other monomer of its generation copolymerization saponified.
This Polarizer is advantageously made by following operation; during by the adhesive layer diaphragm that lamination is formed by the cyclic olefine resin on surface of polyethenol series light polarizing film or two surfaces; adopting carbamate is that the potpourri of aqueous solution of cementing agent and polyvinyl alcohol resin is as cementing agent; wherein this polyvinyl alcohol resin be vinyl acetate and can be with the multipolymer of other monomer of its generation copolymerization saponified; and after the aqueous solution that with carbamate is cementing agent and polyvinyl alcohol resin 5 minutes with the interior surface that is used for light polarizing film or diaphragm, again the two is carried out lamination.
The effect of invention
According to the present invention, compare with the situation that adopts use cementing agent of the prior art, can produce the Polarizer of polyethenol series light polarizing film and the cohesiveness excellence of the diaphragm that forms by the cyclic olefine resin.
Embodiment
Below the present invention is described in detail.Light polarizing film is the film that polyvinyl alcohol resin forms, and for example can enumerate at absorption iodine on the polyvinyl alcohol resin film and makes its orientation and the iodine polarizing film that forms, absorption bitintability dyestuff and make its orientation and the dyestuff that forms is a light polarizing film on the polyvinyl alcohol resin film.The part of these films is implemented processed and the polyenoid that forms is a light polarizing film etc.Polyvinyl alcohol resin usually can be by being that resin carries out saponification and obtains to polyvinyl acetate.As polyvinyl acetate is resin, except polyvinyl acetate as the homopolymer of vinyl acetate, can also for vinyl acetate with can with the multipolymer of other monomer of its generation copolymerization, for example for poly-(ethene-vinyl acetate) multipolymer etc.Also can carry out modification, for example also can adopt aldehydes modified polyethylene formal, tygon acetal, polyvinyl butyral etc. these polyvinyl alcohol resins.
Iodine polarizing film and dyestuff are that light polarizing film is passed through to carry out uniaxial extension and dye with iodine or bitintability dyestuff on the former anti-film (former anti-Off ィ Le system) that these polyvinyl alcohol resins form, and make absorption of iodine or bitintability dyestuff and orientation.The thickness of polyethenol series light polarizing film is for for example about about 5-50 μ m.
In the present invention, by surface of this polyethenol series light polarizing film or two-sided on lamination by the diaphragm that the cyclic olefine resin forms, make Polarizer.As the cyclic olefine resin, for example for having as norborene or encircling the thermoplastic resin of the monomeric unit that the cyclic olefin (cycloolefin) of norborneol alkene monomer forms more.This cyclic olefine resin also can be cycloolefin and chain alkene or the multipolymer with aromatics of vinyl.In addition, it also is effective importing polar group.
Under the situation of multipolymer that is cycloolefin and chain alkene or aromatics,, can enumerate ethene or propylene etc. as the example of chain alkene with vinyl.In addition, as the example of aromatics, can enumerate the styrene of styrene, α-Jia Jibenyixi, the replacement of nuclear alkyl etc. with vinyl.In this multipolymer, the monomeric unit that is formed by cycloolefin for example can be for about 15-50 mole % at 50 moles of % or following.In particular for cycloolefin, chain alkene with have under the situation of terpolymer of aromatics of vinyl, can be still less by the monomeric unit that cycloolefin forms than this amount.In this terpolymer, the monomeric unit that is formed by chain alkene is generally about 5-80 mole %, and the monomeric unit with aromatics formation of vinyl is generally about 5-80 mole %.
As commercially available thermoplasticity cyclic olefine resin, for example be " Topas ", " ァ-ト Application ", " ZEONOR " and " ZEONEX " that Japanese ゼ ォ Application (strain) is sold that ジ ェ ィ エ ス ァ-Le (strain) is sold of the Ticona society sale of Germany's (De イ Star), " the ァ ペ Le " that Mitsui Chemicals (strain) is sold etc.This cyclic olefine resin becomes film by the system film, when the system film, can adopt the known method of solvent casting method, extrusion by melting etc.The cyclic olefine resin molding of making film also has commercially available, for example has " エ ス シ-Na " and " SCA40 " that ponding chemical industry (strain) sells etc.
The thickness of diaphragm is got over Bao Yuehao, if but thin excessively, intensity can reduce, and processability on the other hand, if blocked up, variation will take place the transparency and descend, perhaps the problem of the required elongated grade of curing time behind the lamination.Therefore the suitable thickness of diaphragm for example is about 5-200 μ m, is preferably 10-150 μ m, more preferably 20-100 μ m.
This diaphragm that is formed by the cyclic olefine resin can be fitted on the one side of light polarizing film, also can be fitted on its two sides.Under the situation of the diaphragm that applying on the two sides of light polarizing film is formed by the cyclic olefine resin, the kind of 2 diaphragms can be identical, also can be different.Under the situation of the diaphragm that applying on the surface of light polarizing film is formed by the cyclic olefine resin, the diaphragm that can on its relative one side, fit and form by the resin beyond the cyclic olefine resin.As the diaphragm that forms by the resin beyond the cyclic olefine resin; can exemplify out the film that becomes as the acetyl fibre prime system resin-shaped of triacetyl cellulose or diacetyl cellulose, the film of the optical transparence excellence of the film that forms as the polyester based resin of polyethylene terephthalate or PEN, polyester terephthalate butanediol ester, the film that polycarbonate-based resin forms etc.
Light polarizing film and be that to adopt carbamate be that the hybrid adhesive of cementing agent and polyvinyl alcohol resin carries out lamination by the diaphragm that the cyclic olefine resin forms.Under the situation of the diaphragm that lamination on the two sides of light polarizing film is formed by the cyclic olefine resin, the diaphragm that on the two sides of light polarizing film, forms by the cyclic olefine resin by this hybrid adhesive bonding.On the other hand, under the situation of the diaphragm forms by the cyclic olefine resin when fitting on the surface of light polarizing film, when the diaphragm that applying forms by other resin is gone up on another surface, on the two sides of light polarizing film, can use identical cementing agent; Also can when light polarizing film is bondd with the diaphragm that is formed by the cyclic olefine resin, use above-mentioned hybrid adhesive, when light polarizing film is bondd with the diaphragm that is formed by the resin beyond the cyclic olefine resin, use other cementing agent.During diaphragm that for example lamination is become by acetyl fibre prime system resin-shaped on a surface of light polarizing film, when the two is bondd, in fact also can adopt the cementing agent that forms by polyvinyl alcohol resin.
At carbamate is in the cementing agent, the one-pack-type cementing agent that existence is formed by the prepolymer with isocyanate group end group, with by having with the main agents of the functional group of isocyanates radical reaction, particularly hydroxyl and having the dual liquid type cementing agent that the hardening agent of isocyanate group forms, can use any cementing agent in the present invention.In one-pack-type, isocyanate group end group and on every side moisture, for example with light polarizing film in moisture or airborne reaction of moisture, perhaps, produce cohesiveness with the reactive with active hydrogen of film surface.
As constituting the dual liquid type carbamate is a wherein side the main agents with hydroxyl of cementing agent, and can enumerate polyether glycol, polyester polyol, acrylic acid series multiple alcohol, ethene-vinyl acetate is polyvalent alcohol, polyamide-based polyvalent alcohol etc.Polyether glycol for example is polyglycol, polypropylene glycol, ethylene oxide/propylene oxide multipolymer etc.Polyester polyol, for example condensed polymer of dibasic acid and dibasic alcohol.Acrylic acid series multiple alcohol for example is such as (methyl) acrylate with hydroxyl of (methyl) hydroxy-ethyl acrylate, (methyl) hydroxypropyl acrylate, (methyl) acrylic acid hydroxy butyl ester etc. and the multipolymer of methacrylic acid or its Arrcostab.Ethene-vinyl acetate is that polyvalent alcohol is an ethylene-vinyl acetate copolymer, or the partly-hydrolysed thing of its multipolymer more than ternary that further forms with other monomer copolymerization that copolymerization can take place, as the 3rd monomer that uses in this case, can enumerate chain olefines, vinyl ethers, unsaturated nitrile, ethylene halide base, allyl compound, vinyl silyl compound beyond unsaturated carbon acids and salt thereof, esters of acrylic acid, the ethene, have the monomer of taken place free radical polymerization of the aromatics etc. of vinyl.Polyamide-based polyvalent alcohol, for example when making above-mentioned polyester polyol by as raw material and with the diamines of ethylene diamine, trimethylene diamine, hexamethylene diamine etc., can form amido link.
In the main agents of carbamate cementing agent, it is reagent that existence is dissolved in the organic solvent that forms in the organic solvent with polyvalent alcohol, and polyvalent alcohol is dissolved in the water system reagent that forms in the water.In the present invention, owing to being the aqueous solution of cementing agent and polyvinyl alcohol resin with this carbamate, the therefore preferred water system reagent that adopts.In the commercially available product as the main agents of dual liquid type carbamate cementing agent, " EL-436A " that has Japan モ-ト Application (strain) to sell as polyester polyol as acrylic acid series multiple alcohol, has " EA-W151A " that Japan モ-ト Application (strain) sells etc.
As constituting the dual liquid type carbamate is cementing agent the opposing party's hardening agent, for have the compound of isocyanate group in molecular end, for example except the toluylene group diisocyanate is arranged, methyl diphenylene diisocyanate, hexamethylene diisocyanate, the polyisocynate monomer of isophorone diisocyanate etc. is attached to these multiple molecules the addition product that forms on the polyvalent alcohol as trimethylolpropane in addition, 3 molecule diisocyanate partly form the 3 officials energy fulminuric acid ester of fulminuric acid ester ring at an isocyanate group end group of each molecule, 3 molecule diisocyanate at an isocyanate group end group of each molecule partly by hydration, decarbonate and form such as modification body of the polyisocyanates of biuret etc.
The hardening agent of dual liquid type carbamates cementing agent is preferably and can be dispersed in the type of using in the water.As the commercially available product of the hardening agent of dual liquid type carbamates cementing agent, for example be any hardening agent of Japan モ-ト Application (strain) " EL-436B " and " EA-W151B " that sell etc.
The polyvinyl alcohol resin that mixes with the carbamates cementing agent is to use with the form of aqueous solution.In polyvinyl alcohol resin as cementing agent; handle the alcotex obtain except the polyvinyl acetate (PVA) as the vinyl acetate homopolymer being carried out saponification; also have Dichlorodiphenyl Acetate ethene and can carry out saponification with the multipolymer of other monomer of its generation copolymerization and handle the ethenol system copolymer that obtains; further the hydroxyl part of these polymkeric substance is carried out the modified polyvinylalcohol based polymer of modification, for example adopt known method to make acetoacetyl modified polyethylene alcohol that the saponified and diketen reaction of the homopolymer of vinyl acetate or multipolymer obtains etc.In the present invention, in this polyethenol series cementing agent, also can adopt as vinyl acetate with can with the saponified ethenol system copolymer of the multipolymer of other monomer of its generation copolymerization.Under the situation that adopts alcotex, be difficult to obtain enough cohesive forces between polyethenol series light polarizing film and the cyclic olefine resin.
In the multipolymer of vinyl acetate and other monomer, with vinyl acetate during as main body, the copolymerization ratio of the two is: vinyl acetate is about 70-99.9 mole %, and other monomer is about 0.1-30 mole %.Other monomer with the vinyl acetate copolymerization, unsaturated carboxylic acid class and salt thereof, esters of acrylic acid, chain olefines, vinyl ester, unsaturated nitrile, halogen vinyl, allyl compound, vinyl silicyl are arranged, have the aromatics of vinyl etc., the multipolymer of wherein preferred and unsaturated carboxylic acid class and salt copolymerization thereof.But, as the polyvinyl alcohol resin that constitutes cementing agent of the present invention, preferably adopt multipolymer saponified of vinyl acetate and monomer with carboxyl, in other words, preferably adopt carboxy-modified polyvinyl alcohol (PVA).Described in this manual " carboxyl " is for comprising-notion of COOH and salt thereof.
As commercially available carboxy-modified polyvinyl alcohol (PVA), for example can enumerate " DR-0415 ", " AF-17 " that Japanese vinegar PVC Port バ-Le (strain) is sold respectively, " AT-17 " and " AP-17 " of " the Network ラ レ Port バ-Le KL506 " that sell respectively by (strain) Network ラ レ, " Network ラ レ Port バ-Le KL318 " and " Network ラ レ Port バ-Le KL118 " and " go-セ Na-Le T-330 " and " go-セ Na-Le T-350 " sold by Japanese synthetic chemical industry (strain), electrochemical industry (strain) sale etc.
The molecular weight of polyvinyl alcohol resin is generally about 10,000-1,000,000, is preferably 20,000-400,000, more preferably 40,000-120,000.This polyvinyl alcohol resin is being dissolved in the water, when forming cementing agent, the concentration of polyvinyl alcohol resin is being not particularly limited, for example the weight ratio of polyvinyl alcohol resin/water is about (0.1-10)/100, is preferably (1-5)/100.
In the cementing agent that for carbamate is cementing agent and polyvinyl alcohol resin potpourri, further mixed water dissolubility epoxy compound, glyoxal, glutaraldehyde, zinc chloride, melamine based compound etc.These compositions are blended in the aqueous solution of polyvinyl alcohol resin usually.Particularly, preferably cooperate water miscible epoxy compound in order to improve the cementing agent of diaphragm and light polarizing film.
As the soluble epoxide compound, can exemplify out as the polyalkylene polyamine of diethylene triamine or trien with as the polyamide polyamine that obtains of the dicarboxylic acid reaction of hexane diacid, and the daiamid epoxy resin that itself and chloropropylene oxide is reacted obtain etc.As the commercially available product of this daiamid epoxy resin, for example be " the ス ミ レ-ズ レ ジ Application 650 " and " ス ミ レ-ズ レ ジ Application 675 " of Sumitomo Chemical (strain) sale, " WS-525 " that Japanese PMC (strain) sells etc.
In the time of in the aqueous solution that the soluble epoxide compound is engaged in polyvinyl alcohol resin, the ratio of soluble epoxide compound/polyvinyl alcohol resin is generally about (5-100)/100 in the weight ratio of solid constituent, is preferably (5-50)/100.If the amount of soluble epoxide compound is littler than this scope, prevent that then the effect that diaphragm peels off is little, and too much the time, adhesive layer becomes fragile easily.And in the aqueous solution of this polyvinyl alcohol resin, can add the soluble epoxide compound, also can add zinc chloride, tin chloride, boron zinc fluoride, tertiary amine, quaternary ammonium salt, imidazolium compounds etc.
In the present invention, with carbamate is that the potpourri of cementing agent and polyvinyl alcohol resin is as cementing agent, the ratio of the two preferably adopts: with respect to 100 weight portion carbamates is the solid constituent of cementing agent, and polyvinyl alcohol resin is counted about the 1-500 weight portion with solid constituent.Be the solid constituent of cementing agent with respect to 100 weight portion carbamates more preferably, polyvinyl alcohol resin is counted the 5-200 weight portion with solid constituent, more preferably the 10-100 weight portion.Ratio that can be the functional group of main agents and hardening agent in the cementing agent according to carbamate etc. is selected aptly.
As improve cementing agent and light polarizing film with and/or the close-burning means of diaphragm; can adopt on light polarizing film and/or diaphragm and apply corona treatment, flame treatment, plasma treatment; the ultraviolet ray irradiation, the surface treatment of plasma coating processing, saponification processing etc.
Applying method to polyethenol series light polarizing film and diaphragm is not particularly limited; for example; can enumerate and on the surface of polyethenol series light polarizing film or diaphragm, be coated with cementing agent equably, overlapping another film on coated face, by modes such as roller fit, dry method etc.
By the mixed amino formic ether is cementing agent and polyvinyl alcohol resin aqueous solution preparation cementing agent; adopt this cementing agent that light polarizing film and diaphragm are carried out lamination; and from being that cementing agent and polyvinyl alcohol resin aqueous solution begin time of carrying out light polarizing film and the diaphragm between the lamination to it is applicable to carbamate, preferably in 5 minutes.If oversize from the time that is mixed into lamination, then produce precipitation or separation in the hybrid adhesive, there is the problem of adhesive property decline and degraded appearance etc.From time of being mixed into lamination more preferably in 3 clocks, more preferably in 1 minute.
Usually behind the preparation hybrid adhesive, be coated with under 15-40 ℃ temperature, binding temperature is usually in the scope about 15-30 ℃.After applying, carry out dried, to remove the solvent of water contained in the cementing agent etc., the baking temperature of this moment is generally 30-85 ℃, is preferably in 40-80 ℃ the scope.After this, 15-85 ℃, preferably 20-50 ℃, more preferably under 35-45 ℃ temperature environment, carry out the maintenance about 0.1-100 days usually, make adhesive cures.If this curing time is oversize, productivity variation then, so be preferably about 0.5-30 days more preferably 1-7 days between curing period.
Thus, by comprising the adhesive layer that carbamate is cementing agent and polyvinyl alcohol resin, the diaphragm of on surface of polyethenol series light polarizing film or two surfaces, fitting and forming by the cyclic olefine resin, thus obtain Polarizer.
In the present invention; for diaphragm; the diaphragm that forms by the cyclic olefine resin particularly; can make it have function as phase retardation film; as the function that improves the briliancy film, as the function of reflectance coating, as the function of semipermeable reflection film; as the function of diffusion barrier, as the optical property of function of optical compensation films etc.At this moment, except by for example on the surface of diaphragm, passing through lamination phasic difference film, improve the briliancy film; reflectance coating, semipermeable reflection film, diffusion barrier; the optically functional film of optical compensation films etc. has beyond these functions it, can also make diaphragm itself have such function.For example, by being implemented to extend, said protection film handles the function that to give this diaphragm phase retardation film.On said protection film; by adopting as special 2002-169025 communique or the special formation micropores of putting down in writing in the 2003-29030 communique such as method of opening opened; perhaps overlapping by the different cholesteric more than 2 layers or 2 layers of centre wavelength that will select reflection, it is had as the function that improves the briliancy film.On said protection film, form metallic film, can make it have function as reflectance coating or semipermeable reflection film by modes such as evaporation or sputters.Comprise the resin solution of particulate by coating on said protection film, can make it have function as diffusion barrier.Further,, and make its orientation, can make it have function as optical compensation films by coating fluid crystallinity compound on said protection film.
Below, by shown in embodiment the present invention is described in further detail, but the present invention is not subjected to the restriction of these examples.In example, the % of expression amount or use amount and part do not have to specify, are weight basis.
Embodiment 1
(a) making of light polarizing film
At thickness is that (degree of polymerization is 2400 for the polyvinyl alcohol film of 75 μ m, saponification degree be 99.9 moles of % or more than) on, carrying out extension ratio with dry method is 5 times uniaxial extension, keep this tense situation, directly it was flooded 60 seconds in 60 ℃ pure water, then the weight ratio of iodine/potassium iodide/water be in 0.05/5/100 the aqueous solution 60 seconds time of dipping dye.After this, be 73 ℃ of times of 300 seconds of dipping down in 6/7.5/100 the aqueous solution in the weight ratio of potassium iodide/boric acid ice.After further dipping time of 10 seconds cleans in 15 ℃ pure water, 50 ℃ dry down, obtain iodine polarizing film.
(b) preparation of cementing agent
As carbamate is cementing agent, in " EL-436A " (solid component concentration is 35% aqueous solution) that 100 parts of Japan モ as the polyester polyol prepolymer of main agents-ト Application (strain) is made, " EL-436B " (effective constituent is 100% product) that cooperates 30 parts of Japan モ-ト Application (strain) to make as the isocyanate-based hardening agent, further add water, with the concentration dilution to 20% of solid constituent.On the other hand, as the polyethenol series cementing agent, 3% aqueous solution of the carboxy-modified polyvinyl alcohol (PVA) " Network ラ レ Port バ-Le KL318 " that preparation (strain) Network ラ レ makes (mol ratio of vinyl acetate and sodium itaconate is that saponified, the saponification degree of about 98: 2 multipolymer is that 85-90 mole %, molecular weight are about 85000).With the carbamate of gained is that cementing agent and polyethenol series aqueous solution are that 1: 1 (weight ratio of solid constituent is 20: 3) mixes according to weight ratio, makes hybrid adhesive.
(c) diaphragm
The thickness that will be made by the cyclic olefine resin " ZEONOR " that Japanese ゼ ォ Application (strain) is made is that the film of 40 μ m then is first diaphragm.The thickness that the Off イ Le system (strain) of further Fuji being drawn a portrait is made be 80 μ m for " the Off ジ Star Network UV80 " of tri acetyl cellulose membrane as second diaphragm.
(d) with the making of the Polarizer of diaphragm
In mixed 1 minute of the hybrid adhesive that (b) method makes, it is coated on the two sides of the iodine polarizing film that (a) make.On one surface with 250Wmin/m
2Condition carry out corona treatment; fit in a surface of first diaphragm of this corona treatment face and above-mentioned cyclic olefine resin being made with the interior time in 30 seconds after this corona treatment; on another surface; second diaphragm that the above-mentioned triacetyl cellulose of handling through saponification with the surface makes is fitted at its saponification treated side; dry 5 minutes time makes Polarizer under 70 ℃.With this Polarizer further 40 ℃ of following maintenances 2 days.
(e) close-burning evaluation: disbonded test
On the surface of first diaphragm that the cyclic olefine resin of the Polarizer after the maintenance makes, with respect to film normal direction inclination 45, see through on the direction of axle and cut blade part, try light polarizing film and this diaphragm are peeled off, still can not peel away.The same experiment of peeling off is also implemented on the surface of second diaphragm that triacetyl cellulose is made, and still still can not peel away.
Embodiment 2
As carbamate is cementing agent, in " EA-W151A " (solid component concentration is 45% aqueous solution) that 100 parts of Japan モ as the acrylic acid series multiple alcohol of main agents-ト Application (strain) is made, " EA-W151B " (effective constituent is 100% product) that cooperates 20 parts of Japan モ-ト Application (strain) to make as the isocyanate-based hardening agent, further add water, with the concentration dilution to 40% of solid constituent.Except preparing carbamate according to this method is cementing agent, do beyond this change, is that cementing agent and polyethenol series aqueous solution are that 1: 1 (weight ratio of solid constituent is 20: 3) mixes according to weight ratio according to the method the same with embodiment 1 with carbamate, make hybrid adhesive, and adopt this cementing agent, make Polarizer according to the method the same with embodiment 1.
On the surface of first diaphragm that the cyclic olefine resin of the Polarizer of gained makes, with respect to film normal direction inclination 45, see through on the direction of axle and cut blade part, try light polarizing film and this diaphragm are peeled off, still can not peel away.The same experiment of peeling off is also implemented on the surface of second diaphragm that triacetyl cellulose is made, and still still can not peel away.
Embodiment 3
The carboxy-modified polyvinyl alcohol (PVA) " Network ラ レ Port バ-Le KL318 " that 3 parts of (strain) Network ラ レ of dissolving make in 100 parts of water, further add " ス ミ レ-ズ レ ジ Application 650 " (solid constituent is 30% aqueous solution) that 1.5 parts of Sumitomo Chemicals as water soluble polyamide epoxy resin (strain) are made, make cementing agent.Except according to this method preparation polyethenol series cementing agent, do beyond this change, according to the method making Polarizer the same with embodiment 1.
On the surface of first diaphragm that the cyclic olefine resin of the Polarizer of gained makes, with respect to film normal direction inclination 45, see through on the direction of axle and cut blade part, try light polarizing film and this diaphragm are peeled off, still can not peel away.The same experiment of peeling off is also implemented on the surface of second diaphragm that triacetyl cellulose is made, and still still can not peel away.
Embodiment 4
At 250Wmin/m
2Condition under cyclic olefine resin film, trade name that ponding chemical industry (strain) is made be that " SCA40 " (thickness is 40 μ m) carried out corona treatment, with it as diaphragm.Except adopting light polarizing film and the cementing agent the same with embodiment 1, said protection film is used on two surfaces of light polarizing film beyond, according to the method making Polarizer the same with embodiment 1.On a surface of the Polarizer of gained, with respect to film normal direction inclination 45, see through on the direction of axle and cut blade part, the diaphragm of light polarizing film and one side is tried to peel off, still can not peel away.
Embodiment 5
Carrying out the thickness that press forming obtains at the multipolymer that with ethene, norborene, cinnamic mol ratio is 49: 22: 29 is on the film of 40 μ m, at 250Wmin/m
2Condition under carry out corona treatment, with it as diaphragm.Except adopting light polarizing film and the cementing agent the same with embodiment 1, said protection film is used on two surfaces of light polarizing film beyond, according to the method making Polarizer the same with embodiment 1.On a surface of the Polarizer of gained, with respect to film normal direction inclination 45, see through on the direction of axle and cut blade part, the diaphragm of light polarizing film and one side is tried to peel off, still can not peel away.
Comparative example 1
Except independent employing carbamate is a cementing agent, wherein main agents is that " EA-W151A ", hardening agent that Japan モ-ト Application (strain) makes are " EA-W151B " that make of Japan モ-ト Application (strain), do not add beyond the aqueous solution of polyvinyl alcohol resin, adopts the method making Polarizer the same with embodiment 2.On the surface of first diaphragm that the cyclic olefine resin of the Polarizer of gained makes, with respect to film normal direction inclination 45, see through on the direction of axle and cut blade part, try light polarizing film and this diaphragm are peeled off, can peel away.The same experiment of peeling off is also implemented on the surface of second diaphragm that triacetyl cellulose is made, but can not peel away.
Comparative example 2
Except the polyethenol series cementing agent that water soluble polyamide epoxy resin makes is added in independent employing in carboxy-modified polyvinyl alcohol water solution, and do not add beyond the urethanes class cementing agent, adopt the method making Polarizer the same with embodiment 3.On the surface of first diaphragm that the cycloolefin resinoid of the Polarizer of gained makes, with respect to film normal direction inclination 45, see through on the direction of axle and cut blade part, try light polarizing film and this diaphragm are peeled off, can peel away.The same experiment of peeling off is also implemented on the surface of second diaphragm that triacetyl cellulose is made, but can not peel away.
Comparative example 3
Except using solution from the polyvinyl alcohol (PVA) " 163-03045 " bought with the pure pharmaceutical worker's industry of light (strain) (saponification degree is about 88%, the degree of polymerization be about 500) 4.8%, adopt the method making Polarizer the same with embodiment 1 as the polyethenol series cementing agent.On the surface of first diaphragm that the cyclic olefine resin of the Polarizer of gained makes, with respect to film normal direction inclination 45, see through on the direction of axle and cut blade part, try light polarizing film and this diaphragm are peeled off, can peel away.The same experiment of peeling off is also implemented on the surface of second diaphragm that triacetyl cellulose is made, but can not peel away.
Comparative example 4
After at carbamate being 1 hour after cementing agent and the polyvinyl alcohol resin aqueous solution, beyond applying light polarizing film and the diaphragm, adopt the method making Polarizer the same with embodiment 3.The result produces precipitation, the degraded appearance of the Polarizer of gained in mixed liquor.
Claims (4)
1. Polarizer; it is the Polarizer that forms by the adhesive layer diaphragm that lamination is formed by the cyclic olefine resin on surface of polyethenol series light polarizing film or two surfaces; it is characterized by; it is cementing agent, polyvinyl alcohol resin and soluble epoxide compound that this adhesive layer contains carbamate; this carbamate is that cementing agent is a dual liquid type; its principal ingredient is wanted reagent and isocyanate-based hardening agent for the polyester owner, and this polyvinyl alcohol resin is multipolymer saponified of vinyl acetate and the monomer with carboxyl.
2. Polarizer as claimed in claim 1 is characterized by, and the cyclic olefine resin is the multipolymer that contains the monomeric unit that is formed by cycloolefin with the ratio of 15-50 mole %.
3. Polarizer as claimed in claim 1 or 2, wherein the diaphragm that is formed by the cyclic olefine resin has from as the function of phase retardation film, as the function that improves the briliancy film, as the function of reflectance coating, as the function of semipermeable reflection film, as the function of selecting the function of diffusion barrier and the function as optical compensation films.
4. the manufacture method of Polarizer; wherein; thereby when making Polarizer by the adhesive layer diaphragm that lamination is formed by the cyclic olefine resin on surface of polyethenol series light polarizing film or two surfaces; have following operation: adopting carbamate is cementing agent; the potpourri of the aqueous solution of polyvinyl alcohol resin and soluble epoxide compound is as cementing agent; wherein this carbamate is that cementing agent is a dual liquid type; its principal ingredient is wanted reagent and isocyanate-based hardening agent for the polyester owner; this polyvinyl alcohol resin is multipolymer saponified of vinyl acetate and the monomer with carboxyl; and be cementing agent with this carbamate; after the aqueous solution of polyvinyl alcohol resin and soluble epoxide compound 5 minutes with the interior surface that is used for light polarizing film or diaphragm, again the two is carried out lamination.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
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JP111283/03 | 2003-04-16 | ||
JP2003111283 | 2003-04-16 | ||
JP111283/2003 | 2003-04-16 |
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CN100381839C true CN100381839C (en) | 2008-04-16 |
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CNB2004100451591A Expired - Fee Related CN100381839C (en) | 2003-04-16 | 2004-04-14 | polarizing board and its mfg. method |
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KR (1) | KR101076252B1 (en) |
CN (1) | CN100381839C (en) |
TW (1) | TW200428043A (en) |
Families Citing this family (11)
Publication number | Priority date | Publication date | Assignee | Title |
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KR100771950B1 (en) * | 2005-04-19 | 2007-10-31 | 주식회사 에이스 디지텍 | Polarizing Film with PET Polarizer Protection Layer and Picture Display Device using the same |
WO2007086709A1 (en) * | 2006-01-27 | 2007-08-02 | Lg Chem. Ltd. | Adhesive for polarizer plate and method for manufacturing the same |
JP5016568B2 (en) * | 2007-08-20 | 2012-09-05 | 富士フイルム株式会社 | Optical compensation film, manufacturing method thereof, polarizing plate and liquid crystal display device using the same |
US20090053516A1 (en) * | 2007-08-24 | 2009-02-26 | Jerome Vivien Davidovits | Durable light-polarizing articles and method of making the same |
CN101597467B (en) * | 2008-06-04 | 2011-07-20 | 明基材料股份有限公司 | Plastic material for polarizing plate |
CN101424764B (en) * | 2008-10-08 | 2010-06-16 | 深圳市盛波光电科技有限公司 | Method for enhancing inner protection film hydrophilicity of polaroid |
WO2011129531A2 (en) * | 2010-04-12 | 2011-10-20 | 동우화인켐 주식회사 | Polarising plate and a liquid-crystal display device comprising the same |
KR101674116B1 (en) * | 2010-04-12 | 2016-11-08 | 동우 화인켐 주식회사 | A polarizing plate |
KR101028277B1 (en) | 2010-05-25 | 2011-04-11 | 엘지이노텍 주식회사 | Light emitting device, method for fabricating the light emitting device, light emitting device package and lighting unit |
JP2014534988A (en) * | 2012-05-30 | 2014-12-25 | エルジー・ケム・リミテッド | Aqueous composition, optical film including the same, polarizing plate using the same, and liquid crystal display device |
TWI727371B (en) * | 2019-07-16 | 2021-05-11 | 住華科技股份有限公司 | Polarizer structure and manufacturing method thereof |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH08101307A (en) * | 1994-10-03 | 1996-04-16 | Kuraray Co Ltd | Polarizing plate |
JPH10130402A (en) * | 1996-10-29 | 1998-05-19 | Nippon Zeon Co Ltd | Polymer film and preparation thereof |
JP2000321430A (en) * | 1999-05-14 | 2000-11-24 | Gunze Ltd | Polarizing plate and its production |
JP2000321432A (en) * | 1999-03-08 | 2000-11-24 | Sekisui Chem Co Ltd | Polarizing plate |
WO2001048519A1 (en) * | 1999-12-28 | 2001-07-05 | Gunze Co., Ltd | Polarizing plate |
-
2004
- 2004-04-09 TW TW093109989A patent/TW200428043A/en not_active IP Right Cessation
- 2004-04-13 KR KR1020040025261A patent/KR101076252B1/en not_active IP Right Cessation
- 2004-04-14 CN CNB2004100451591A patent/CN100381839C/en not_active Expired - Fee Related
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH08101307A (en) * | 1994-10-03 | 1996-04-16 | Kuraray Co Ltd | Polarizing plate |
JPH10130402A (en) * | 1996-10-29 | 1998-05-19 | Nippon Zeon Co Ltd | Polymer film and preparation thereof |
JP2000321432A (en) * | 1999-03-08 | 2000-11-24 | Sekisui Chem Co Ltd | Polarizing plate |
JP2000321430A (en) * | 1999-05-14 | 2000-11-24 | Gunze Ltd | Polarizing plate and its production |
WO2001048519A1 (en) * | 1999-12-28 | 2001-07-05 | Gunze Co., Ltd | Polarizing plate |
Also Published As
Publication number | Publication date |
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KR101076252B1 (en) | 2011-10-26 |
CN1540373A (en) | 2004-10-27 |
TWI354124B (en) | 2011-12-11 |
KR20040090456A (en) | 2004-10-25 |
TW200428043A (en) | 2004-12-16 |
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