CN101137917A - Iodine-containing polarizing film, process for producing the same, and polarizer comprising the same - Google Patents
Iodine-containing polarizing film, process for producing the same, and polarizer comprising the same Download PDFInfo
- Publication number
- CN101137917A CN101137917A CNA2006800077219A CN200680007721A CN101137917A CN 101137917 A CN101137917 A CN 101137917A CN A2006800077219 A CNA2006800077219 A CN A2006800077219A CN 200680007721 A CN200680007721 A CN 200680007721A CN 101137917 A CN101137917 A CN 101137917A
- Authority
- CN
- China
- Prior art keywords
- acid
- polarizing film
- solution
- light polarizing
- film
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 238000000034 method Methods 0.000 title claims description 60
- 239000011630 iodine Substances 0.000 title description 31
- 229910052740 iodine Inorganic materials 0.000 title description 31
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 title description 29
- 230000008569 process Effects 0.000 title description 14
- 229920002451 polyvinyl alcohol Polymers 0.000 claims abstract description 85
- 239000004372 Polyvinyl alcohol Substances 0.000 claims abstract description 80
- 229920005989 resin Polymers 0.000 claims abstract description 57
- 239000011347 resin Substances 0.000 claims abstract description 57
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 claims abstract description 43
- 239000004327 boric acid Substances 0.000 claims abstract description 43
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 claims abstract description 39
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 claims abstract description 23
- 150000007524 organic acids Chemical class 0.000 claims abstract description 21
- 239000000243 solution Substances 0.000 claims description 102
- 239000000126 substance Substances 0.000 claims description 72
- 239000000463 material Substances 0.000 claims description 62
- 230000002378 acidificating effect Effects 0.000 claims description 61
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 60
- 238000004132 cross linking Methods 0.000 claims description 60
- 238000012545 processing Methods 0.000 claims description 60
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 55
- 238000010306 acid treatment Methods 0.000 claims description 36
- 239000003795 chemical substances by application Substances 0.000 claims description 32
- 239000007864 aqueous solution Substances 0.000 claims description 31
- 239000002253 acid Substances 0.000 claims description 23
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 22
- 239000001164 aluminium sulphate Substances 0.000 claims description 20
- 235000011128 aluminium sulphate Nutrition 0.000 claims description 20
- BUACSMWVFUNQET-UHFFFAOYSA-H dialuminum;trisulfate;hydrate Chemical compound O.[Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O BUACSMWVFUNQET-UHFFFAOYSA-H 0.000 claims description 20
- 238000004519 manufacturing process Methods 0.000 claims description 20
- 235000011054 acetic acid Nutrition 0.000 claims description 19
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 claims description 18
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 18
- 239000011707 mineral Substances 0.000 claims description 18
- 235000015165 citric acid Nutrition 0.000 claims description 17
- 150000002148 esters Chemical class 0.000 claims description 13
- 230000001681 protective effect Effects 0.000 claims description 13
- JLDSOYXADOWAKB-UHFFFAOYSA-N aluminium nitrate Chemical compound [Al+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O JLDSOYXADOWAKB-UHFFFAOYSA-N 0.000 claims description 12
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 claims description 12
- 239000004973 liquid crystal related substance Substances 0.000 claims description 10
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 8
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 claims description 6
- 235000006408 oxalic acid Nutrition 0.000 claims description 6
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 claims description 5
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 claims description 5
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 claims description 5
- 239000001630 malic acid Substances 0.000 claims description 5
- 235000011090 malic acid Nutrition 0.000 claims description 5
- 229940095064 tartrate Drugs 0.000 claims description 5
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 claims description 4
- 229910017604 nitric acid Inorganic materials 0.000 claims description 4
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 claims description 3
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 3
- FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 claims description 3
- 235000019253 formic acid Nutrition 0.000 claims description 3
- 238000012360 testing method Methods 0.000 abstract description 57
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 22
- 150000003839 salts Chemical class 0.000 abstract description 8
- 239000003431 cross linking reagent Substances 0.000 abstract description 3
- 230000007423 decrease Effects 0.000 abstract description 3
- 150000007522 mineralic acids Chemical class 0.000 abstract 1
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 33
- 230000008859 change Effects 0.000 description 26
- 230000010287 polarization Effects 0.000 description 22
- 239000007767 bonding agent Substances 0.000 description 21
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 20
- 238000004140 cleaning Methods 0.000 description 16
- 238000005516 engineering process Methods 0.000 description 15
- 239000010410 layer Substances 0.000 description 13
- 235000010755 mineral Nutrition 0.000 description 13
- -1 polyethylene Polymers 0.000 description 13
- 230000000052 comparative effect Effects 0.000 description 12
- 150000004677 hydrates Chemical class 0.000 description 12
- 239000002904 solvent Substances 0.000 description 12
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 12
- 238000004043 dyeing Methods 0.000 description 11
- 235000007715 potassium iodide Nutrition 0.000 description 11
- 230000008961 swelling Effects 0.000 description 10
- 238000001035 drying Methods 0.000 description 9
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 8
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 8
- 150000001875 compounds Chemical class 0.000 description 8
- 239000000975 dye Substances 0.000 description 8
- 150000004820 halides Chemical class 0.000 description 7
- 239000003960 organic solvent Substances 0.000 description 7
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- LEQAOMBKQFMDFZ-UHFFFAOYSA-N alpha-ketodiacetal Natural products O=CC=O LEQAOMBKQFMDFZ-UHFFFAOYSA-N 0.000 description 6
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 6
- ZADPBFCGQRWHPN-UHFFFAOYSA-N boronic acid Chemical compound OBO ZADPBFCGQRWHPN-UHFFFAOYSA-N 0.000 description 6
- 238000007654 immersion Methods 0.000 description 6
- 239000011592 zinc chloride Substances 0.000 description 6
- 235000005074 zinc chloride Nutrition 0.000 description 6
- 238000010521 absorption reaction Methods 0.000 description 5
- 238000007598 dipping method Methods 0.000 description 5
- 125000005843 halogen group Chemical group 0.000 description 5
- 230000001976 improved effect Effects 0.000 description 5
- 239000002609 medium Substances 0.000 description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 235000019270 ammonium chloride Nutrition 0.000 description 4
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000012467 final product Substances 0.000 description 4
- 239000012530 fluid Substances 0.000 description 4
- 229910001629 magnesium chloride Inorganic materials 0.000 description 4
- 235000011147 magnesium chloride Nutrition 0.000 description 4
- 239000000178 monomer Substances 0.000 description 4
- 230000035699 permeability Effects 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- OPPFIPBEHRZBOT-UHFFFAOYSA-N 1,1-bis(oxiran-2-ylmethoxy)propan-1-ol Chemical compound C1OC1COC(O)(CC)OCC1CO1 OPPFIPBEHRZBOT-UHFFFAOYSA-N 0.000 description 3
- WHQOKFZWSDOTQP-UHFFFAOYSA-N 2,3-dihydroxypropyl 4-aminobenzoate Chemical compound NC1=CC=C(C(=O)OCC(O)CO)C=C1 WHQOKFZWSDOTQP-UHFFFAOYSA-N 0.000 description 3
- XZXYQEHISUMZAT-UHFFFAOYSA-N 2-[(2-hydroxy-5-methylphenyl)methyl]-4-methylphenol Chemical compound CC1=CC=C(O)C(CC=2C(=CC=C(C)C=2)O)=C1 XZXYQEHISUMZAT-UHFFFAOYSA-N 0.000 description 3
- LRWZZZWJMFNZIK-UHFFFAOYSA-N 2-chloro-3-methyloxirane Chemical compound CC1OC1Cl LRWZZZWJMFNZIK-UHFFFAOYSA-N 0.000 description 3
- KMNCBSZOIQAUFX-UHFFFAOYSA-N 2-ethoxy-1,2-diphenylethanone Chemical compound C=1C=CC=CC=1C(OCC)C(=O)C1=CC=CC=C1 KMNCBSZOIQAUFX-UHFFFAOYSA-N 0.000 description 3
- MKTOIPPVFPJEQO-UHFFFAOYSA-N 4-(3-carboxypropanoylperoxy)-4-oxobutanoic acid Chemical compound OC(=O)CCC(=O)OOC(=O)CCC(O)=O MKTOIPPVFPJEQO-UHFFFAOYSA-N 0.000 description 3
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 3
- 229920002284 Cellulose triacetate Polymers 0.000 description 3
- 229920003656 Daiamid® Polymers 0.000 description 3
- 239000004593 Epoxy Substances 0.000 description 3
- SXRSQZLOMIGNAQ-UHFFFAOYSA-N Glutaraldehyde Chemical compound O=CCCCC=O SXRSQZLOMIGNAQ-UHFFFAOYSA-N 0.000 description 3
- 229920001744 Polyaldehyde Polymers 0.000 description 3
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 3
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 3
- 159000000013 aluminium salts Chemical class 0.000 description 3
- 229910000329 aluminium sulfate Inorganic materials 0.000 description 3
- 229940107816 ammonium iodide Drugs 0.000 description 3
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 3
- OHJMTUPIZMNBFR-UHFFFAOYSA-N biuret Chemical compound NC(=O)NC(N)=O OHJMTUPIZMNBFR-UHFFFAOYSA-N 0.000 description 3
- 229910052796 boron Inorganic materials 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 235000011187 glycerol Nutrition 0.000 description 3
- 229940015043 glyoxal Drugs 0.000 description 3
- 239000012948 isocyanate Substances 0.000 description 3
- 150000002513 isocyanates Chemical class 0.000 description 3
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Natural products OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 3
- 238000003475 lamination Methods 0.000 description 3
- 239000011259 mixed solution Substances 0.000 description 3
- 239000012046 mixed solvent Substances 0.000 description 3
- 230000003287 optical effect Effects 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- HNBFUFIYQWYCDM-UHFFFAOYSA-N oxygen(2-) sulfane titanium(4+) Chemical compound [O--].[O--].S.[Ti+4] HNBFUFIYQWYCDM-UHFFFAOYSA-N 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 229920002689 polyvinyl acetate Polymers 0.000 description 3
- 239000011118 polyvinyl acetate Substances 0.000 description 3
- 238000007127 saponification reaction Methods 0.000 description 3
- FVAUCKIRQBBSSJ-UHFFFAOYSA-M sodium iodide Chemical compound [Na+].[I-] FVAUCKIRQBBSSJ-UHFFFAOYSA-M 0.000 description 3
- 239000010936 titanium Substances 0.000 description 3
- 229910052719 titanium Inorganic materials 0.000 description 3
- UAYWVJHJZHQCIE-UHFFFAOYSA-L zinc iodide Chemical class I[Zn]I UAYWVJHJZHQCIE-UHFFFAOYSA-L 0.000 description 3
- UWFRVQVNYNPBEF-UHFFFAOYSA-N 1-(2,4-dimethylphenyl)propan-1-one Chemical compound CCC(=O)C1=CC=C(C)C=C1C UWFRVQVNYNPBEF-UHFFFAOYSA-N 0.000 description 2
- 229910021584 Cobalt(II) iodide Inorganic materials 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 235000010724 Wisteria floribunda Nutrition 0.000 description 2
- NNLVGZFZQQXQNW-ADJNRHBOSA-N [(2r,3r,4s,5r,6s)-4,5-diacetyloxy-3-[(2s,3r,4s,5r,6r)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6s)-4,5,6-triacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxyoxan-2-yl]methyl acetate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](OC(C)=O)[C@H]1OC(C)=O)O[C@H]1[C@@H]([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1)OC(C)=O)COC(=O)C)[C@@H]1[C@@H](COC(C)=O)O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O NNLVGZFZQQXQNW-ADJNRHBOSA-N 0.000 description 2
- 229940081735 acetylcellulose Drugs 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 239000012736 aqueous medium Substances 0.000 description 2
- 229910021538 borax Inorganic materials 0.000 description 2
- 229920002301 cellulose acetate Polymers 0.000 description 2
- 150000001805 chlorine compounds Chemical class 0.000 description 2
- 239000011247 coating layer Substances 0.000 description 2
- AVWLPUQJODERGA-UHFFFAOYSA-L cobalt(2+);diiodide Chemical compound [Co+2].[I-].[I-] AVWLPUQJODERGA-UHFFFAOYSA-L 0.000 description 2
- 238000007334 copolymerization reaction Methods 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 239000011261 inert gas Substances 0.000 description 2
- 150000002496 iodine Chemical class 0.000 description 2
- 230000007774 longterm Effects 0.000 description 2
- 239000006166 lysate Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 210000004379 membrane Anatomy 0.000 description 2
- 239000012528 membrane Substances 0.000 description 2
- 210000000713 mesentery Anatomy 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000010695 polyglycol Substances 0.000 description 2
- 229920000151 polyglycol Polymers 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 239000004328 sodium tetraborate Substances 0.000 description 2
- 235000010339 sodium tetraborate Nutrition 0.000 description 2
- 238000001179 sorption measurement Methods 0.000 description 2
- 238000002834 transmittance Methods 0.000 description 2
- WYXIGTJNYDDFFH-UHFFFAOYSA-Q triazanium;borate Chemical compound [NH4+].[NH4+].[NH4+].[O-]B([O-])[O-] WYXIGTJNYDDFFH-UHFFFAOYSA-Q 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- 230000000007 visual effect Effects 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N Acrylic acid Chemical class OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 1
- BRDWIEOJOWJCLU-LTGWCKQJSA-N GS-441524 Chemical compound C=1C=C2C(N)=NC=NN2C=1[C@]1(C#N)O[C@H](CO)[C@@H](O)[C@H]1O BRDWIEOJOWJCLU-LTGWCKQJSA-N 0.000 description 1
- DKNPRRRKHAEUMW-UHFFFAOYSA-N Iodine aqueous Chemical compound [K+].I[I-]I DKNPRRRKHAEUMW-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
- 150000001241 acetals Chemical class 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 229910001514 alkali metal chloride Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 239000004411 aluminium Substances 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000007860 aryl ester derivatives Chemical class 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000012267 brine Substances 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 210000004027 cell Anatomy 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- HRYZWHHZPQKTII-UHFFFAOYSA-N chloroethane Chemical compound CCCl HRYZWHHZPQKTII-UHFFFAOYSA-N 0.000 description 1
- HGAZMNJKRQFZKS-UHFFFAOYSA-N chloroethene;ethenyl acetate Chemical compound ClC=C.CC(=O)OC=C HGAZMNJKRQFZKS-UHFFFAOYSA-N 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000001276 controlling effect Effects 0.000 description 1
- 210000002858 crystal cell Anatomy 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 229920005994 diacetyl cellulose Polymers 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 238000005401 electroluminescence Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 235000013373 food additive Nutrition 0.000 description 1
- 239000002778 food additive Substances 0.000 description 1
- 238000002309 gasification Methods 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 150000003949 imides Chemical class 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000001802 infusion Methods 0.000 description 1
- 239000002346 layers by function Substances 0.000 description 1
- 238000003913 materials processing Methods 0.000 description 1
- 238000002715 modification method Methods 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 238000005457 optimization Methods 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920005672 polyolefin resin Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 150000004671 saturated fatty acids Chemical class 0.000 description 1
- 230000002000 scavenging effect Effects 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 235000009518 sodium iodide Nutrition 0.000 description 1
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical class O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 238000007669 thermal treatment Methods 0.000 description 1
- 150000003752 zinc compounds Chemical class 0.000 description 1
Landscapes
- Polarising Elements (AREA)
Abstract
A polarizing film obtained by stretching a polyvinyl alcohol resin film containing iodine, an iodide, and a crosslinking agent and/or water resistance imparter and then treating the film with a solution which contains either an inorganic acid other than boric acid or a salt thereof and/or an organic acid in an amount of 0.0001-5.0 wt.% and which has a pH of desirably 2-5, preferably 2.2-5. The polarizing film is excellent in wet heat durability and is less apt to decrease in polarizing properties in a wet heat durability test. The polarizing film obtained according to the preferred embodiment is excellent also in dry heat durability.
Description
Technical field
The present invention relates to the iodine polarizing plate of iodine polarizing film and manufacture method thereof and this iodine polarizing film of use.
Background technology
Polarizer normally is oriented on the film formed light polarizing film of polyvinyl alcohol resin in the iodine or the dichroic dye absorption of dichromatism pigment; its single or double forms by diaphragms such as bond layer stickup cellulose triacetates, and it can be used in liquid crystal indicator etc.Use the formed Polarizer of light polarizing film of dichromatism pigment iodine to be called the iodine polarizing plate, on the other hand, it is Polarizer that the formed Polarizer of light polarizing film of the dichroic dye of use dichromatism pigment is called dyestuff.With dyestuff be Polarizer relatively, the iodine polarizing plate has high permeability and high degree of polarization, also promptly demonstrates high-contrast, thereby is widely used in common LCD, LCD TV, mobile phone, PDA etc.Though but the iodine polarizing plate is a Polarizer better than dyestuff on optical characteristics, but being not so good as dyestuff on optical durability is Polarizer, for example, when the iodine polarizing plate is placed the environment of hot and humid degree, produce decolouring and the low inferior problem of transmitance increase degree of polarization.And, aspect xeothermic permanance, place that can to produce degree of polarization under the high temperature low.For having high permeability, high degree of polarization, high-contrast; and the requirement of excellent heat resistance and humidity resistance Polarizer; patent documentation 1, patent documentation 2 have been put down in writing the improvement method of diaphragm; patent documentation 3 and patent documentation 4 have been put down in writing the modification method of the bonding agent of bonding cellulose triacetate diaphragm, make damp and hot permanance improve.In addition, also there are obstructed over-protective film or bonding agent to improve permanance, but by handling the example that the polyvinyl alcohol resin film improves iodine polarizing plate permanance.One of them is that acid treatment or the pH control of passing through that is recorded in patent documentation 5,6,7 and 8 improves permanance.For example: patent documentation 5 discloses a kind of light polarizing film, and it is the polyvinyl alcohol resin stretched film that the polyvinyl alcohol resin film immersion that the polyvinyl alcohol resin film that contains boride is made also stretches in acidic aqueous solution, and improves permanance.In addition, patent documentation 6 discloses a kind of manufacture method of light polarizing film, and it is that the polyvinyl alcohol resin film is carried out oxidation in the oxidation bath of the oxygenants such as hydrogen peroxide that contain the alkali metal containing iodide, makes it have excellent humidity resistance.Patent documentation 7 discloses a kind of manufacture method of iodine polarizing film, and it is to handle uniaxial tension and the directed polyvinyl alcohol (PVA) mesentery of absorption in the boric acid aqueous solution below pH4.5, and improves humidity resistance.Patent documentation 8 discloses a kind of polarisation (light polarizing film), and the pH value of solution was 1.0～5.0 when it was dissolved in water.
[patent documentation 1]
Japanese kokai publication hei 8-5836
[patent documentation 2]
TOHKEMY 2001-272534
[patent documentation 3]
Japanese kokai publication hei 2004-12578
[patent documentation 4]
Japanese kokai publication hei 9-269413
[patent documentation 5]
Japanese kokai publication hei 6-254958
[patent documentation 6]
Japanese kokai publication hei 7-104126
[patent documentation 7]
TOHKEMY 2001-83329
[patent documentation 8]
TOHKEMY 2005-62458
Summary of the invention
Put down in writing the made polyvinyl alcohol resin film immersion of the polyvinyl alcohol resin film that will contain boride in acidic aqueous solution and method at patent documentation 5 with its stretching, during stretching, in the aqueous solution (being called dye bath) of the boronic acid containing that is flooded, iodine and potassium iodide, can make the light polarizing film of gained can't obtain the problem that sufficient permanance is improved effect by polyvinyl alcohol resin film stripping acidic materials.In addition, also have in the patent documentation 6 because of before stretching and in regulating the oxidation bath of pH, to handle, make and by polyvinyl alcohol resin film stripping oxygenant in stretch bath, to make the light polarizing film of gained can't obtain the problem that sufficient humidity resistance improves effect when stretching.The borated aqueous solution of patent documentation 7 record remains on pH≤handle below 4.5, yet when handling acid with boric acid, the treatment effeciency variation of polyvinyl alcohol resin film and acidic materials produces the deviation of processing in the film.For example, among the embodiment of patent documentation 7, the degree of polarization when handling with the boronic acid containing treating fluid of pH=3.4 becomes 1.3, and the degree of polarization during pH=2.1 becomes 2.0.Even hence one can see that has controlled pH and also can't obtain stable properties in the method, demonstrating not can be because of having controlled the stable permanance that the pH value just can obtain target.And, when the treatment temperature (treating fluid temperature) in the document in the record technology was high, the situation of acidic materials gasification took place.Open relevant a kind of polarisation in the patent documentation 8 is characterized in that this polarisation is made up of the film of stretching polyethylene alcohol film, and the pH value of solution value that is dissolved in water is at 1.0～5.0.But the Polarizer so that this method obtains though damp and hot permanance has raising, for example in the heat resistant test under 90 ℃ of hot environments, might transmitance sharply reduce, and makes with the light source of liquid crystal indicator or environment for use to show deepening gradually.Therefore, can high-level efficiency handle, and make acid concentration stable treated temperature, much less high temperature, even low temperature also can be handled, by handling with acidic materials containing iodine polyvinyl alcohol resin film, make the iodine polarizing plate of the xeothermic permanance of damp and hot permanance raising and tool excellence that ardent demand be arranged with not borated solution.
In order to solve above-mentioned problem, through attentively discovering: after the polyvinyl alcohol resin film drawn that will contain iodine, iodide, crosslinking chemical and/or anti-hydrated agent is handled, again with contain the mineral acid that do not comprise boric acid or its esters and/or organic acid 0.0001～5.0 weight % (below be reduced to wt%.In addition, nothing specializes, % represents weight %) solution (the following acid treatment solution that is also referred to as according to circumstances) handle, the damp and hot permanance of gained light polarizing film improves, transmitance is with low uncertainty, and, the treatment temperature of acidic materials, much less high temperature, even low temperature also can be handled, make that acidic materials are non-volatile and be applicable to stable treated, moreover, acid treatment is controlled at 2～5 with the pH value of solution, more preferably 2.2～5, be controlled at 2.4≤pH＜6.0 o'clock in addition according to circumstances, xeothermic permanance also improves, in addition, and compared with using boric acid and acidic materials that the pH value is≤4.5 solution simultaneously, by handling with the solution of 2.4≤pH of while halide and acidic materials＜6.0 without boric acid, and when carrying out using dried after acidic materials are handled, the deviation that can obtain optical characteristics is few, damp and hot permanance height, and the Polarizer of xeothermic excellent in te pins of durability, thereby finished the present invention.
That is, the present invention relates to:
(1) a kind of light polarizing film, it is after the polyvinyl alcohol resin film that will contain iodine, iodide, crosslinking chemical and/or anti-hydrated agent carries out stretch processing, handles obtaining again with the solution (hereinafter referred to as acid treatment solution) that contains the mineral acid that do not comprise boric acid or its esters and/or organic acid 0.0001～5.0wt%;
(2) as (1) described light polarizing film, wherein, acid treatment is 2≤pH≤5 with the pH value of solution;
(3) as (1) described light polarizing film, it is after the polyvinyl alcohol resin film that will contain iodine, iodide, crosslinking chemical and/or anti-hydrated agent carries out stretch processing, is that the acid treatment of 2.4≤pH＜6.0 gets with solution-treated with the pH value again;
(4) as (1) described light polarizing film, it is characterized in that, in the mineral acid that does not comprise boric acid or its esters and/or organic acid solution, contain halogenide;
(5), wherein, do not comprise that the mineral acid of boric acid or its esters are wantonly more than a kind or more than 2 kinds in aluminium sulphate, aluminum chloride, aluminium nitrate or the sulfuric acid as (1) described light polarizing film;
(6), wherein, do not comprise that the mineral acid of boric acid or its esters are aluminium sulphate as the described light polarizing film in (1)～(2);
(7) as each described light polarizing film in (1)～(6), it is by getting to contain the organic acid solution-treated, and wherein, organic acid is carboxylic acid and/or the 'alpha '-hydroxy acids more than a kind;
(8) as (7) described light polarizing film, it is by getting to contain the organic acid solution-treated, and wherein, organic acid is wantonly more than a kind or a kind in citric acid, oxalic acid, malic acid, tartrate or the acetic acid;
(9) as each described light polarizing film in (1)～(8), wherein, the stretching ratio of the described polyvinyl alcohol resin film after the stretching is 3～8 times before stretching;
As (1) or (9) described light polarizing film, it is characterized in that (10) employed crosslinking chemical and/or anti-hydrated agent are boric acid during stretch processing;
(11) a kind of Polarizer, the single or double of each described light polarizing film is provided with protective seam in its (1)～(9) that are above-mentioned;
(12) a kind of liquid crystal indicator is characterized in that having (11) described Polarizer;
(13) a kind of manufacture method of light polarizing film is characterized in that, after the polyvinyl alcohol resin film that will contain iodine, iodide, crosslinking chemical and/or anti-hydrated agent carries out stretch processing, is the acid treatment solution-treated of 2.4≤pH＜6.0 again with the pH value;
(14) a kind of manufacture method of Polarizer, it is characterized in that, after the polyvinyl alcohol resin film that will contain iodine, iodide, crosslinking chemical and/or anti-hydrated agent carries out stretch processing, be that the single or double of the light polarizing film that gets with solution-treated of the acid treatment of 2.4≤pH＜6.0 is provided with protective seam with the pH value again;
(15) a kind of manufacture method of light polarizing film, it is characterized in that the polyvinyl alcohol resin film that will contain iodine, iodide, crosslinking chemical carries out stretch processing after, be the acid treatment solution-treated of 2.2≤pH≤5 again with the pH value;
(16) a kind of manufacture method of light polarizing film, it is characterized in that, after the polyvinyl alcohol resin film that will contain iodine, iodide, crosslinking chemical and/or anti-hydrated agent carries out stretch processing, handle to contain the mineral acid that do not comprise boric acid or the solution (hereinafter referred to as acid treatment solution) of its esters and/or organic acid 0.0001～5.0wt% again;
(17) as (15) described light polarizing film manufacture method, wherein, acid treatment solution is the aqueous solution that contains at least a acidic materials selected among the group who is made up of sulfuric acid, hydrochloric acid, nitric acid, aluminium sulphate, aluminum chloride, aluminium nitrate, formic acid, citric acid, chloracetic acid, acetic acid, oxalic acid, malic acid and tartrate;
(18) as (16) or (17) described light polarizing film manufacture method, wherein, acid treatment is 2～5 with the pH value of solution.
The invention effect
The light polarizing film that the present invention obtains is to handle with acidic materials after stretching again, and therefore acidic materials can not brought in the dye bath; In addition,, do not take place to separate out the problem of being brought, make and stably to make light polarizing film industrial because of boric acid owing to do not use boric acid after stretching.In addition, under hygrothermal environment, for example temperature is 65 ℃, relative humidity is under 93% the condition, the variation of transmitance and degree of polarization lowly less, and optimum condition can obtain under arid and hot environment when making down, even for example place 90 ℃, the light polarizing film of the excellence that transmitance is with low uncertainty or Polarizer.By using light polarizing film of the present invention as mentioned above or Polarizer, can guarantee the long-standing exhibit stabilization of LCD.
Embodiment
Below describe the present invention in detail.
The manufacture method that constitutes the polyvinyl alcohol resin of light polarizing film there is no particular restriction, can use known method to make.Described manufacture method for example, can be resin saponification and obtaining with polyvinyl acetate.Polyvinyl acetate is a resin, except the polyvinyl acetate of vinyl acetate list polymers, also have vinyl acetate and can with the multipolymer of other monomer of its copolymerization.With other monomer of vinyl acetate copolymerization, for example, unsaturated carboxylic acid class, olefines, ethene ethers, unsaturated sulfonic acid class etc.The saponification degree of polyvinyl alcohol resin normally about 85 to 100mol%, preferred 95mol%.This polyvinyl alcohol resin can be by further sex change, for example, and with the polyvinyl formal of aldehydes sex change, Pioloform, polyvinyl acetal etc.The degree of polymerization of polyvinyl alcohol resin is usually 1,000～10 in addition, and about 000, preferred about 1,500～5,000.
The film that this polyvinyl alcohol resin is made can be used as the raw material film.There is no particular restriction for the film-forming method of polyvinyl alcohol resin, available known method system film.At this moment, but in the polyvinyl alcohol resin film glycerine of plasticizer-containing, ethylene glycol, propylene glycol and low-molecular-weight polyglycol etc.The content of plastifier is 5 to 20wt%, preferred 8～15wt%.There is no particular restriction for the thickness of the raw material film of being made by polyvinyl alcohol resin, preferred 5～150 μ m, more preferably 10～100 μ m.
At first implement swelling for above-mentioned polyvinyl alcohol resin film (below be also referred to as the PVA film) and handle (also claiming swelling technology).Swelling is handled by 30 seconds～10 minutes mode of dipping in 20 to 50 ℃ solution and is undertaken.The solution preferred water of this moment also can be used the mixed solution of water-miscible organic solvent such as glycerine, ethanol, ethylene glycol, propylene glycol or low-molecular-weight polyglycol or water and organic solvent.When the Production Time of making light polarizing film is shortened,, can omit swelling technology because of swelling being arranged when iodine and the iodide processing.
After the swelling technology, the solution-treated (hereinafter referred to as dyeing) of polyvinyl alcohol resin film to contain iodine and iodide.Disposal route preferably impregnated in this solution, also can or be coated on the polyvinyl alcohol resin film and handles this solution coat.As the solvent of solution for example, preferred water, but be not limited thereto.Iodide for example can use, iodate alkali metal compound, ammonium iodide, cobaltous iodide or zinc iodides etc. such as potassium iodide, but be not limited thereto usually preferred iodate alkali metal compound, more preferably potassium iodide.Preferred 0.0001～the 0.5wt% of iodine concentration, 0 more preferably .001～0.4wt%.Preferred 5～50 ℃ of the treatment temperature of this technology, more preferably 5～40 ℃, most preferably 10～30 ℃.Processing time can be different because of the adsorption concentration of iodine and iodide, though can suitably adjust, preferably is adjusted into 30 seconds～6 minutes, more preferably 1～5 minute.After finishing, this processing before carrying out next technology, can clean.The solvent that cleans generally can make water.By cleaning, can limit iodine and iodide and move on in the next treating fluid.
When carrying out the processing of iodine and iodide, can in solution, add crosslinking chemical and/or anti-hydrated agent.And typically use crosslinking chemical.There is no particular restriction as crosslinking chemical, usually preferred boric acid.Crosslinking chemical, for example preferred 0.1～5.0wt% of interpolation concentration of boric acid, more preferably 2～4wt%.Can use the described material in back about anti-hydrated agent.Preferred 5～50 ℃ of the treatment temperature of this technology, more preferably 5～40 ℃, most preferably 10～30 ℃.Processing time is different because of the adsorption concentration of iodine and iodide, though can suitably adjust, preferred 30 seconds～6 minutes, more preferably 1～5 minute.This can clean before carrying out next technology after handling.The solvent that cleans generally is a water.Can limit iodine and iodide move on in the next treating fluid by cleaning.
In the present invention, when containing the polyvinyl alcohol resin film of iodine, iodide, crosslinking chemical and/or anti-hydrated agent, the PVA film not necessarily contains iodine, iodide, crosslinking chemical and/or anti-hydrated agent itself at least, also can comprise through after above-mentioned dyeing processing and crosslinking chemical and/or the processing of anti-hydrated agent the situation that iodine, iodide, crosslinking chemical and/or anti-hydrated agent exist with reacted form in the PVA film.As the PVA film that contains iodine, iodide, crosslinking chemical and/or anti-hydrated agent, preferably contain iodine, iodide and crosslinking chemical (preferred boron).
Usually behind above-mentioned dyeing, carry out crosslinking chemical and handle (being also referred to as the crosslinking chemical treatment process).Crosslinking chemical is handled the available solution that contains crosslinking chemical and is carried out via the processing of polyvinyl alcohol resin film.Though also can in the presence of crosslinking chemical, carry out dyeing as mentioned above, after finishing, usually preferred dyeing carries out.This moment, crosslinking chemical was handled by carrying out with the solution-treated that contains crosslinking chemical the polyvinyl alcohol resin film of this dyeing gained (below be also referred to as dyed PVA film).Use contain the disposal route of this cross-linking agent solution usually preferred with dyed PVA film immersion in the method for this solution, but this solution coat or the method that is coated on the polyvinyl alcohol resin film also can.This dipping can carry out before following stretch processing or can carry out simultaneously with this stretch processing.When being the dry type stretching method, this pulling method preferably before stretching, carries out crosslinking Treatment; Preferably carry out simultaneously during for the wet type pulling method with this stretch processing.For example can use titanium sub-group compound, diglycidyl ether of ethylene glycol or the daiamid epoxy chloropropane etc. of the multicomponent isocyanate based compound of polyaldehydes such as boride, glyoxal or glutaraldehyde, biuret type, isocyanuric acid ester type or block type etc. such as boric acid or its salt (for example alkali metal salt such as borax or ammonium borate etc.), sulphur titanium dioxide etc. as crosslinking chemical.Usually preferred boride, more preferably boric acid.In addition, in containing the solution of crosslinking chemical, can make anti-hydrated agent coexistence.Have as anti-hydrated agent: succinic acid peroxide, ammonium persulfate, Calcium perchlorate, benzoin ethyl ether, diglycidyl ether of ethylene glycol, propanetriol-diglycidyl-ether, ammonium chloride, magnesium chloride or zinc chloride etc., preferred ammonium chloride, magnesium chloride or zinc chloride etc.Solvent when handling as crosslinking chemical for example can use: water, pure series solvent, ethylene glycol series solvent, glycerine or its mixed solvent etc., preferred water usually.Concentration at the crosslinking chemical that contains cross-linking agent solution is different according to the kind of the crosslinking chemical that uses, and can not be about 0.1～10wt/vol% of solvent usually without exception; With boric acid is example, and then 0.1～6.0wt/vol% concentration of preferred solvent is handled, more preferably 2～4wt/vol%.5～60 ℃ of preferred process temperature, more preferably 5～40 ℃.Preferred 30 seconds～6 minutes of processing time, more preferably 1～5 minute.
Then stretched (preferred uniaxial tension) (below be also referred to as uniaxial tension technology) in order to make above-mentioned dyed PVA film or PVA film dyed and that crosslinking chemical is handled have polarity.Drawing process uses wet type pulling method or dry type stretching method all can.The dry type stretching method is used the PVA film of handling through crosslinking chemical usually.Though the wet type pulling method can use the PVA film of handling through crosslinking chemical, right dyed PVA film to use the Non-crosslinked agent to handle usually preferably carries out crosslinking chemical and handles when stretching.
The dry type stretching method carries out the mode of its stretching via above-mentioned film is heated in gas medium usually.Can use air or inert gas etc. as this gas medium, because of considering economically etc. used air usually.When air is used as medium, in about normal temperature～180 ℃, preferably will stretch through the PVA film that crosslinking chemical is handled with the temperature of controlling this medium.When medium is inert gas etc., can the condition identical with air carry out or according to the condition of situation at high temperature more under carry out also can.This stretch processing is preferably carried out under relative humidity is 20～95% environment in addition.Can consider for example to use as the heating drawing process of film, regional pulling method, roller add hot-drawing method, pressurization pulling method or infrared ray and add hot-drawing method etc. between roller, so are not restricted to this type of drawing process.Stretch processing once (one section) is carried out, but also the above multistage processing of secondary (two sections) is carried out.Preferred 3～8 times of the stretching ratio of this moment, more preferably 5～7 times.
The wet type pulling method usually with above-mentioned film immersion in the aqueous medium of mixed solution of water, water-miscible organic solvent or water and this organic solvent etc., carry out in the mode that adds hot-stretch usually.Preferably in the solution that contains crosslinking chemical and/or anti-hydrated agent the dipping above-mentioned film state and stretch.Preferred 3～8 times of stretching ratio, more preferably 5～7 times.Be stretching in 40～60 ℃ and carry out, preferably be heated in this aqueous medium of 45～55 ℃ and stretch.Can enumerate above-mentioned material as crosslinking chemical, for example, the titanium sub-group compound of the multicomponent isocyanate based compound of polyaldehydes such as borides such as boric acid, borax or ammonium borate, glyoxal or glutaraldehyde, biuret type, isocyanuric acid ester type or block type etc., sulphur titanium dioxide etc., diglycidyl ether of ethylene glycol or daiamid epoxy chloropropane etc.The preferred boride of crosslinking chemical, more preferably boric acid.Also can enumerate above-mentioned material as anti-hydrated agent, for example, succinic acid peroxide, ammonium persulfate, Calcium perchlorate, benzoin ethyl ether, ethylene glycol diglycidylether, propanetriol-diglycidyl-ether, ammonium chloride, magnesium chloride or zinc chloride etc.The concentration of crosslinking chemical and/or anti-hydrated agent is for for example, preferred 0.5～8wt%, more preferably 2.0～4.0wt%.Stretching time is applicable to 30 seconds～20 minutes, preferred 2～5 minutes.Stretch processing once (one section) is carried out, but also the above multistage processing of secondary (two sections) is carried out.
Feature among the present invention is that (below be also referred to as acid treatment solution) in the above-mentioned solution that is containing the mineral acid that does not comprise boric acid of 0.0001～5.0 weight % or its esters and/or organic acid (the following acidic materials that also abbreviate as) through the PVA of uniaxial tension film (following also can singly be called uniaxial tension PVA film) handled.By this processing the damp and hot permanance of light polarizing film is improved, xeothermic permanance is improved.Below also can singly claim this to be treated to " utilizing the processing of acidic materials " according to situation.The processing that utilizes acidic materials usually preferably with the PVA film immersion of above-mentioned stretching in the solution that contains acidic materials (mixed solution of preferred aqueous solutions, water-miscible organic solvent or water and this organic solvent).
After carrying out above-mentioned stretch processing, because of separating out or the absorption of foreign matter of crosslinking chemical arranged, therefore can before utilizing the acidic materials processing, carry out the cleaning (hereinafter referred to as cleaning) on film surface on film surface.In this cleaning, can clean by boronic acid containing solution, the situation that the foreign matter generation is arranged on the film surface in next technology or dry back because of the cleaning of carrying out with boronic acid containing solution according to situation, usually when cleaning, utilize not borated solution to carry out the wherein cleaning of preferred water.In addition, in the time can utilizing boronic acid containing solution to clean, be included in after this cleaning finishes, carry out acid treatment, then drying etc. also has the treatment process that makes the film surface not generate foreign matter after finishing cleaning with boronic acid containing solution.Scavenging period is applicable to 1 second～5 minutes.There is no particular restriction for wash number, optionally can be once, also can be the repeatedly cleaning more than 2 times.
Carry out or carry out respectively the solution-treated of the preferred halide of PVA film that will stretch after the stretch processing simultaneously with the processing that utilizes acidic materials.The purpose of this processing is the adjustment of form and aspect and the raising of polarized light property (below be also referred to as halogenide handle).Disposal route can have: the method for the PVA film that dipping stretches in this solution, on this PVA film surface with this solution coat or application etc., preferred infusion process.This halogenide is handled preferred and is utilized the processing of acidic materials to carry out simultaneously in addition.With said method handle this PVA film and get final product to contain acidic materials and halid solution simultaneously this moment.As halogenide for example, chlorides such as the alkali metal chloride compound of iodide such as iodate alkali metal compound, ammonium iodide, cobaltous iodide or zinc iodide, potassium chloride and sodium chloride etc. such as preferred potassium iodide and sodium iodide or zinc chloride, more preferably water-soluble substances.Chloride and iodide are preferred iodide, preferred iodate alkali metal compound, more preferably potassium iodide in the iodide.Preferred 0.5～the 15wt% of halid concentration, more preferably 3～8wt%.Treatment temperature is for example preferred below 5～50 ℃ in addition, more preferably 20～40 ℃.For example 1 second～5 minutes processing time got final product, but as considering the stability of polarisation face internal characteristic, then preferred 5～30 seconds.When being purpose, form and aspect can not omit to contain the treatment process of this halide solution to adjust.
Utilize the processing of acidic materials and after finish halogenide and handle, carry out the drying (being also referred to as drying process later on) of film.Be good with air dry when carrying out drying, but the compression of available cylinder or utilize air knife or suction roll etc. carries out the removal of film surface moisture in order to improve drying efficiency, with and/or the drying of blowing also can.Treatment temperature can be handled down at 20～90 ℃, preferably 40～80 ℃ of following processors.Preferred 30 seconds～20 minutes of processing time, more preferably 2～10 minutes.
Up to the present, in treatment process,, for example have as the solvent of Treatment Solution, water, pure series solvent or ethylene glycol series solvent equal solvent, but be not to be defined in this.The solution that mixes with alcohols as water and mixed solvent of dimethyl sulfoxide (DMSO) and water etc. in addition then can make the mixed solvent of water and water-miscible organic solvent.Preferably make water.
Utilize the processing of acidic materials among the present invention so long as after the polyvinyl alcohol (PVA) mesentery drawn (preferred uniaxial tension) that will contain iodine, iodide, crosslinking chemical and/or anti-hydrated agent is arranged, under any technology, carry out all can.For example with this stretching after cleaning or the processing that utilizes acidic materials simultaneously of halogenide treatment process, above-mentioned film stretch the back or finish if necessary in cleaning after, then independently utilize any of processing of acidic materials all can.Optionally clean after stretching (preferred uniaxial tension) with polarity is finished, then utilize the processing (also can be described as acid treatment according to circumstances) of acidic materials.Also can in the technology of plural number, carry out in addition.And more preferably with the PVA film immersion of drawn in containing acidic materials and halid solution, carry out the processing of acidic materials and the method that halogenide is handled simultaneously.Utilize the processing of acidic materials to carry out if necessary in containing down in the Treatment Solution of the crosslinking chemical that do not comprise boric acid and/or anti-hydrated agent with the coexistence of this acidic materials.The concentration that is used in the acidic materials in the Treatment Solution that acidic materials are handled is usually about the scope of 0.0001～5.0wt%, preferred 0.0005～2wt%, more preferably 0.001～1wt%, more preferably 0.01～2wt% also according to circumstances.PH value with this Treatment Solution is preferably 1.0≤pH＜6.0 in addition.More preferably the pH value is the close limit below 6.0 more than 2, also more preferably about 2.1～5.As long as the acid treatment temperature and time can be reached effect of the present invention, there is no particular restriction, and treatment temperature is below 5～60 ℃ usually, and preferred about 10～40 ℃, the processing time is 2～300 seconds, preferred 3～60 seconds, and more preferably about 5～40 seconds.
In cleaning, can clean simultaneously and acid treatment when cleaning according to circumstances with the solution that contains acidic materials.Treatment temperature is preferred below 5～60 ℃, more preferably 10～40 ℃.Preferred 2～300 seconds of processing time, more preferably 2～60 seconds be.
Halogenide is handled and can carried out after the stretch processing or after the cleaning treatment, can carry out separately or carry out simultaneously with acid treatment in acid treatment process as above-mentioned.It is this PVA film (following also can abbreviate stretched film as) after solution with halide is applicable to above-mentioned stretching that halogenide is handled, in the technology of handling this stretched film, usually preferably as above-mentioned acid treatment process in carrying out simultaneously with acid treatment.To contain the disposal route of this halide solution as this film, as long as this solution is applicable to this stretched film surface, any method all can.Usually preferably this stretched film be impregnated in this solution.When carrying out simultaneously, get final product with this this film of halid solution-treated to contain above-mentioned acidic materials simultaneously with above-mentioned acid treatment process.Preferably this stretched film be impregnated in the solution that contains both.Be used in the scope of the common preferred 0.5～15wt% of halid concentration of the halide solution of handling with halogenide.When carrying out the halogenide processing simultaneously, can use the halogenide that contains above-mentioned concentration range, and contain the acidic materials solution of the scope of 0.0001～5.0wt% with acid treatment.Treatment temperature is preferred below 5～60 ℃ in addition, and more preferably 20～40 ℃, applicable 2 seconds～5 minutes of processing time, preferred 5 seconds～1 minute.
Can use mineral acid and organic acid arbitrarily as acidic materials, further aqueous solution is acid its esters, and preferably the pH value of this brine solution is less than 6 salt, more preferably the pH value greater than 1 less than 5 salt.Mineral acid is the acid of preferably sulfuric acid, hydrochloric acid or nitric acid etc., more preferably sulfuric acid.Salt typically uses the salt of mineral acid, the salt of above-mentioned preferred mineral acid, preferred especially aluminium salt.Have as this type of salt: aluminium sulphate, aluminum chloride or aluminium nitrate etc.One of aluminium sulphate is preferred especially.The zinc chloride that is used as anti-hydrated agent etc. because of its pH value of aqueous solution not in above-mentioned pH scope, therefore be not included in the acidic materials of the present invention.Organic acid can be enumerated usually as carboxylic acids, preferably has the C1-C4 saturated fatty acid that hydroxyl or halogen replace, and the water-soluble organic acid with 'alpha '-hydroxy acids skeleton is one of preferred.Concrete example for example, formic acid, citric acid, chloracetic acid, acetic acid, oxalic acid, malic acid or tartrate etc., optimization citric acid or acetic acid, most preferably acetic acid is.Acidic materials can once use and a kind ofly maybe can mix two or more uses.In these type of acidic materials, because of aluminium sulphate improves the effect height of damp and hot permanance, for one of preferred especially.In organic acid, citric acid, acetic acid, oxalic acid etc. generally are to use as food additives in addition, say it is preferred acidic materials on the viewpoint by environment or safety.
The example of preferred acidic materials can enumerate as: aluminium salt (preferably being formed the aluminium salt of selecting mineral acid in the group by sulfuric acid, hydrochloric acid or nitric acid), citric acid and acetic acid by sulfuric acid, mineral acid are become at least a acidic materials selected in the group, preferably sulfuric acid aluminium or acetic acid.
In containing the solution of acidic materials, can contain crosslinking chemical (crosslinking chemical beyond the preferred boric acid) and/or anti-hydrated agent simultaneously.Crosslinking chemical beyond the boric acid is except for example using: the multicomponent isocyanate of polyaldehydes such as glyoxal or glutaraldehyde, biuret type, isocyanuric acid ester type block type etc. is that other also can use diglycidyl ether of ethylene glycol or daiamid epoxy chloropropane etc. the titanium sub-group compound of compound, sulphur titanium dioxide etc. etc.Anti-hydrated agent is for example: succinic acid peroxide, ammonium persulfate, Calcium perchlorate, benzoin ethyl ether, ethylene glycol diglycidylether, propanetriol-diglycidyl-ether, ammonium chloride, magnesium chloride or zinc chloride etc.
When containing the acidic materials solution-treated, the pH value of this solution also is an important parameter.The low then damp and hot permanance height of light polarizing film of pH value.When but the pH value is too low, the decomposition and the polyenoidization of polyvinyl alcohol resin may take place.In dry heat test, for example transmitance has the situation that variation more than 1% takes place in 90 ℃ heat resistant test thus.Result thus, the pH value that will contain acidic materials solution (acid treatment solution) are adjusted into the product that 1.0≤pH＜6.0 o'clock are suitable for obtaining the high humidity heat durability, the more preferably scope of 2≤pH≤5.When also going for the high product of xeothermic permanance, preferred pH value is more than 2, more preferably more than 2.2 less than 6.0 narrow range, also more preferably from about 2.2 to 5.Further preferred according to circumstances 2.4≤pH＜6.0, more preferably 2.4≤pH≤5.0, the also more preferably scope of 2.4≤pH≤4.0.
The decay few person of preferred light polarizing film of the present invention for having high humidity heat durability and high level cadre's heat durability, transmitance simultaneously.So excellent light polarizing film of the present invention is dissolved this light polarizing film pH value of aqueous solution in the scope of 5.0＜pH＜6.0, and this is one of parameter that becomes excellent light polarizing film among the present invention.More preferably 5.1～5.6 scope of this pH value of aqueous solution in addition.More preferably the situation of the light polarizing film in 5.2＜pH＜5.6 o'clock is more for this pH value of aqueous solution in addition, and most preferably the pH value of this solution of light polarizing film is 5.2＜pH＜5.4.The pH value of aqueous solution of dissolving light polarizing film of the present invention can record as follows.
Promptly, the light polarizing film of the present invention that obtains cut out 0.0380g after drying process finished, place the stopper wide-necked bottle (the precious corporate system stopper wide-necked bottle SV-30 of institute of manufacturing) that is placed with 10cc distilled water, the tight loam cake of bolt, be dipped in the boiling water-bath 2 hours, and obtained being dissolved with the aqueous solution of light polarizing film, and this aqueous solution is cooled to 25 ℃, measure this pH value of aqueous solution with AS ONE corporate system pH Controller pp-01, resulting pH value is the pH value of aqueous solution of dissolving light polarizing film of the present invention.In this aqueous solution, light polarizing film such as water-soluble solution person get final product, and need there is no need all dissolvings as the light polarizing film of the present invention of sample, and the light polarizing film of sample itself can be the state of half dissolving or swelling fully etc.But the not dissolving of the light polarizing film of sample part preferably is no more than 20wt%.
The polyvinyl alcohol resin film that obtains with the solution-treated that contains 0.0001～5.0wt% acidic materials, with the solution-treated of acidic materials concentration height (the pH value is low person), the light polarizing film lysate that is obtained shows low pH value.This expression concentration of acidic materials and the pH value of light polarizing film have correlativity, can show the pH value of may command light polarizing film lysate by the acidic materials in the control and treatment solution, also, and the degree of treatment of light polarizing film that may command obtains.The concentration of acidic materials is important factor when making light polarizing film.
The preferable production process of light polarizing film of the present invention is for example in order to make the PVA film through iodine and iodide dyeing have polarity, preferably to stretch 3～8 times preferred about about 4～7 times (preferred uniaxial tension) in the aqueous solution that contains crosslinking chemical (being preferably boron); Or will be through the dyeing of iodine and iodide and the PVA film of handling (preferred boron is handled) through crosslinking chemical with dry type stretching method (preferred folk prescription is to stretching) 3～8 times that stretch, preferred about 4～7 times (being preferably uniaxial tension), the stretched film of gained with above-mentioned acid treatment solution, is preferably contained above-mentioned acidic materials and halide solution and carries out the method that acid treatment and halogenide are handled; To can obtain dry light polarizing film of the present invention via drying through the film of this processing.
By above technology the stretching of polyvinyl alcohol resin film is obtained iodine polarizing film of the present invention.
By protective seam being set as Polarizer at single or double at least in the gained light polarizing film.The laminate layers of formed coating layer of protective clear layer usable polymers or film is provided with.Is good as the transparent polymer that forms protective clear layer or film with the transparent polymer or the film of tool high mechanical properties and good thermal stability.And, the moisture barrier property person of preferred tool excellence.Use for example has as the material composition of protective clear layer, as the cellulose ethanoate resin of tri acetyl cellulose or diacetyl cellulose or its film, acryl resin or its film, Corvic or its film, vibrin or its film, poly-aryl esters resin or its film, with as the cyclic olefin of norborene as the polyolefin of the cyclic polyolefin resin of monomer or its film, tygon, polypropylene, ring system or tool norborene skeleton or its multipolymer, main chain/or side chain be resin or polymkeric substance or its film etc. of acid imide and/or acid amides.For polyvinyl alcohol (PVA) can be brought into play as liquid crystal with the function of oriented film, can make it be applicable to that brushing (rubbing) handles or handle with the light oriented film, resin or its film with liquid crystal liquid crystal property are set.The thickness of diaphragm for example is about 0.5 μ m～200 μ m.By being set at single or double, the above identical type of one deck or different types of resin or film make Polarizer.
After one of them surface of acquisition Polarizer sticked on display device, becoming the adhesive linkage that non-surface of exposing face protective seam or film also can be provided with sticker etc.By the setting of adhesive linkage, Polarizer can be pasted on the display device of liquid crystal, organic electroluminescent (EL) etc.
One of them surface of this Polarizer also is the face that exposes of protective seam or film, can have the known various function layers such as liquid crystal application layer that contrast is improved and/or improved at anti-reflecting layer or antiglare layer, hard coating layer, visual angle.Have the preferred finishing of various dynamopathic layers, maybe the film with this function can be pasted by bonding agent or sticker.Various in addition functional layers can be the layer of control phase difference or the known polarizer of film.
When on light polarizing film, protective clear layer being set, when protective seam is the situation of film, be necessary to carry out the lamination of film.The bonding agent of needs is just arranged this moment.Bonding agent is to use the polyethenol series bonding agent.As the polyethenol series bonding agent for example: GOHSENOL NH-26 (Japanese Synesis Company system) or EXCEVAL RS-2117 (KURARAY corporate system) etc., but be not limited thereto.In bonding agent, can add crosslinking chemical and/or anti-hydrated agent.In bonding agent, can contain the acidic materials that concentration is 0.0001～20wt% in addition, preferably contain 0.02～5wt%.In the polyethenol series bonding agent, can use pure maleic anhydride-isobutylene copolymers/or be mixed with the maleic anhydride-isobutylene copolymers bonding agent of crosslinking chemical.As maleic anhydride-isobutylene copolymers, for example, ISOBAM#18 (KURARAY corporate system), ISOBAM#04 (KURARAY corporate system), ammonia sex change ISOBAM#104 (KURARAY corporate system), ammonia sex change ISOBAM#110 (KURARAY corporate system), imidizate ISOBAM#304 (KURARAY corporate system), imidizate ISOBAM#310 (KURARAY corporate system) etc.The crosslinking chemical of this moment can use water-soluble polynary epoxy compound.Water-soluble polynary epoxy compound is for example: DENACOLEX-521 (NagaseChemtex Cor. system), safe special rood (テ ト ラ Star ト)-c (Mitsui aerochemistry corporate system) etc.Can use known bonding agent commonly used such as aethylis carbamas system, acrylic acid series, epoxy system as other bonding agent, and that bonding agent there is no is limited.In addition as the additive of bonding agent, can be simultaneously contain Zinc compounds or halogenide etc. with the concentration of about 0.1～10wt%.About additive also indefinite person.After protective clear layer pasted with bonding agent, temperature drying or thermal treatment by appropriateness can obtain Polarizer.
Even resulting in this way Polarizer of the present invention is placed between long-term under hot and humid environment, the also rare variation of transmitance and degree of polarization, low few because of the transmitance under 90 ℃ hot environment for example in addition, excellent in te pins of durability, and can keep long-term between stable performance.By Polarizer of the present invention being used in LCD or electroluminescence (EL) display device, CRT etc., can obtain image display of the present invention.Particularly under the situation of LCD,, optionally can obtain LCD of the present invention with the bonding agent stickup simultaneously with phase retardation film by with the both sides of Polarizer of the present invention in the liquid crystal cell (cell) that constitutes LCD.Particularly the LCD sharpness of following the image of Polarizer deterioration to show is low and be suppressed for the image display of gained according to this, make stable image can be for a long time between demonstration.
[embodiment]
Further describe the present invention by the following examples, the present invention is not limited to this type of embodiment.Undertaken by following in the evaluation of transmitance shown in the embodiment and degree of polarization in addition.
To paste resulting two Polarizers of diaphragm on the two sides of light polarizing film, the transmitance that its absorption axes direction is become when identical and superimposed is considered as parallel transmitance Tp; Make the vertical transmitance when superimposed of its absorption axes direction be considered as vertical transmitance Tc two Polarizers.
Transmitance T is the wavelength coverage at 380～780nm, obtains the spectrophotometric transmittance τ λ in predetermined wavelength interval d λ (being 10nm at this), calculates according to following formula (1).In the formula, P λ represents that the beam split of standard light (illuminant-C) distributes, and y λ represents 2 degree visual angle isochrome functions (colour-matchingfunctions).
[formula 1]
Spectrophotometric transmittance τ λ measures with spectrophotometer (Hitachi, Ltd's system " U-4100 ").
Degree of polarization Py is obtained with formula (2) by parallel transmitance Tp and vertical transmitance Tc.
Py={ (Tp-Tc)/(Tp+Tc) } 1/2 * 100 formula (2)
PH value in the aqueous solution is measured with AS ONE corporate system pH Controller " pp-01 ".
[embodiment 1]
More than 99%, average degree of polymerization is 2400 polyvinyl alcohol film (KURARAY corporate system trade name: VF-XS) flooded 2 minutes in 40 ℃ warm water, finish swelling and handle 1.30 times of after stretching with saponification degree.The film of gained was flooded 2 minutes down in 30 ℃ in the aqueous solution that contains boric acid (Societa Chimica Larderellos.p.a. corporate system) 28.6g/l, iodine (pure chemical company system) 0.25g/l, potassium iodide (pure chemical company system) 17.7g/l and ammonium iodide (pure chemical company system) 1.0g/l, utilize the dyeing of iodine and iodide to handle.Dyeing being handled the film of back gained handled 5 minutes in containing 50 ℃ aqueous solution of 30.0g/l boric acid on 5.0 times of one side of uniaxial tension on one side.Keep the tight state of handling the gained film through boric acid, in the aqueous solution of adjusting with 50g/l potassium iodide and 0.02g/l aluminium sulphate 14～18 hydrates (with the pure pharmaceutical worker's industry of light corporate system), handled for 15 seconds down in 30 ℃.This moment, pH value of aqueous solution was 4.8.Under 70 ℃, carry out 9 minutes dried with potassium iodide, through the film that acid treatment gets.(Fuji Photo Film Co Ltd.'s system, trade name: TD-80U) lamination obtains Polarizer with tri cellulose acetate membrane through alkali treatment with the polyethenol series bonding agent with the film of dried gained.
The gained Polarizer is cut into the size of 40mm * 40mm, via bonding agent (Japanese chemical drug corporate system, trade name: PTR-3000) paste as test sample with the glass plate of thickness 1mm.This sample is applicable to dry heat test and damp heat test.
The condition of damp heat test is in the environment of 65 ℃ of temperature, relative humidity 93%, measure to place (432 hours) on the 18th preceding with after transmitance and degree of polarization.Ratio when containing the solution-treated of acidic materials when not handling is as the parameter in order to the decline quality of the rising (decolouring) of confirming transmitance and degree of polarization.
The condition of dry heat test is in 90 ℃ of environment of temperature, measure to place (432 hours) on the 18th preceding with after transmitance.The variation of transmitance is good with at absolute value 1.0%, with 1.0% with interior as parameter.Transmitance can produce the influence of the colorrendering quality that can't obtain display device etc. in the variation more than 1.0%, thereby not preferred.In the test findings of dry heat test by the viewed variation of the absolute value of transmitance 1.0% with interior being considered as (well), then be considered as (bad) more than 1.0%.
[embodiment 2]
Change the addition of 14～18 hydrates of the aluminium sulphate among the embodiment 1 into 0.2g/l, the pH value changes into beyond 3.4, makes other identical samples, and compares the permanance of dry heat test and damp heat test.PH value when making the light polarizing film dissolving after the dried is 5.3.
[embodiment 3]
Change 14～18 hydrates of the aluminium sulphate among the embodiment 1 into citric acid (anhydrous) (pure chemical company system), addition is 0.05g/l, and the pH value changes into beyond 4.8, makes other identical samples, and compares the permanance of dry heat test and damp heat test.
[embodiment 4]
Change the addition of the citric acid among the embodiment 3 into 0.07g/l, the pH value changes into beyond 4.3, makes other identical samples, and compares the permanance of dry heat test and damp heat test.
[embodiment 5]
Change the addition of the citric acid among the embodiment 3 into 0.1g/l, the pH value changes into beyond 3.8, makes other identical samples, and compares the permanance of dry heat test and damp heat test.
[embodiment 6]
Change the addition of the citric acid among the embodiment 3 into 0.3g/l, the pH value changes into beyond 2.5, makes other identical samples, and compares the permanance of dry heat test and damp heat test.PH value when making the light polarizing film dissolving after the dried is 5.4.
[embodiment 7]
Change the addition of the citric acid among the embodiment 3 into 0.5g/l, the pH value changes into beyond 2.3, makes other identical samples, and compares the permanance of dry heat test and damp heat test.PH value when making the light polarizing film dissolving after the dried is 5.3.
[embodiment 8]
Change 14～18 hydrates of the aluminium sulphate among the embodiment 1 into acetic acid (pure chemical company system), addition is 0.04g/l, and the pH value of solution changes into beyond 5.1, makes other identical samples, and compares the permanance of dry heat test and damp heat test.
[embodiment 9]
Change the addition of the acetic acid among the embodiment 8 into 0.07g/l, the pH value change into 4.0 outside, make other identical samples, and the permanance of dry heat test and damp heat test relatively.
[embodiment 10]
Change the addition of the acetic acid among the embodiment 8 into 0.11g/l, the pH value changes into beyond 3.8, makes other identical samples, and compares the permanance of dry heat test and damp heat test.
[embodiment 11]
Change the addition of the acetic acid among the embodiment 8 into 0.6g/l, the pH value changes into beyond 3.4, makes other identical samples, and compares the permanance of dry heat test and damp heat test.PH value when making the light polarizing film dissolving after the dried is 5.7.
[embodiment 12]
Change the addition of the acetic acid among the embodiment 8 into 3.0g/l, the pH value changes into beyond 2.6, makes other identical samples, and compares the permanance of dry heat test and damp heat test.PH value when making the light polarizing film dissolving after the dried is 5.4.
[embodiment 13]
Change the addition of the acetic acid among the embodiment 8 into 5.0g/l, the pH value changes into beyond 2.4, makes other identical samples, and compares the permanance of dry heat test and damp heat test.PH value when making the light polarizing film dissolving after the dried is 5.1.
Comparative example 1
Aluminium sulphate 14～18 hydrates in not adding embodiment 1, make other identical samples, and compare the permanance of dry heat test and damp heat test.PH value when making the light polarizing film dissolving after the dried is 6.0.
The measurement result that transmitance in embodiment 1 to 13 and comparative example 1, degree of polarization change is shown in table 1 and table 2.
The damp and hot permanance of table 1 is in the transmitance of test front and back and the variation of degree of polarization
The damp and hot permanance of table 2 is in the transmitance of test front and back and the variation of degree of polarization
Learn that by above embodiment, comparative example the polyvinyl alcohol resin film that contains iodine, iodide of the present invention makes it contain crosslinking chemical, become the film that is applicable to stretch processing, acidic materials except the boric acid that contains 0.0001～5.0wt%, the pH value in the solution of 2.4≤pH＜6.0, handle and light polarizing film, for example become in hygrothermal environment, at the following nondiscoloration of 65 ℃ of temperature, relative humidity 93% and the few light polarizing film or the Polarizer of reduction of degree of polarization.Can obtain at the Polarizer of LCD with high permeability, high-contrast and the high humidity heat durability of light polarizing film.Further learn according to the xeothermic permanance of the resulting light polarizing film of the present invention for example in 90 ℃ dry heat test the variation of transmitance in 1.0%.Learnt that by above result the damp and hot permanance of Polarizer can improve because of the pH value of Treatment Solution, the transmitance that can obtain under xeothermic permanance changes little Polarizer.PH value when on the other hand, the pH value of the pH value of observing Treatment Solution when making the light polarizing film dissolving can find that the solution-treated light polarizing film that heals high with acidic materials concentration is dissolved is lower.Therefore as can be known the concentration of the concentration of acidic materials and light polarizing film between correlationship is arranged.Acidic materials concentration is lower, makes the pH value demonstration in light polarizing film when dissolving be bordering on 6, though dry heat test for example 90 ℃ transmitance can not descend, right damp and hot permanance can reduce gradually.Make the pH value in light polarizing film when dissolving higher as can be known near 5 damp and hot permanance numerical value, pH value 5 when following in the remarkable decline of transmitance meeting of 90 ℃ dry heat test.Learn by above result, the acidic materials of polyvinyl alcohol resin film except the boric acid that contains 0.0001～5.0wt% that will contain iodine, pH value are that damp and hot permanance improves and changes little Polarizer in the transmitance of xeothermic permanance at the resulting Polarizer of the solution-treated of 2.4≤pH＜6.0.
[embodiment A-2]
Change the addition of 14～18 hydrates of the aluminium sulphate among the embodiment 1 into 4.5g/l, the pH value changes into beyond 2.73, makes other identical samples, and compares the permanance under the damp heat test.
[embodiment A-3]
Change 14～18 hydrates of the aluminium sulphate among the embodiment 1 into sulfuric acid (pure chemical company system), addition is 0.2g/l, and the pH value changes into beyond 1.88, makes other identical samples, and compares the permanance under the damp heat test.
[embodiment A-4]
Change 14～18 hydrates of the aluminium sulphate among the embodiment 1 into sulfuric acid (pure chemical company system), addition is 0.03g/l, and the pH value changes into beyond 3.4, and other make identical sample, and compares the permanance under the damp heat test.
[embodiment A-5]
Change 14～18 hydrates of the aluminium sulphate among the embodiment 1 into aluminium nitrate (with the pure pharmaceutical worker's industry of light corporate system), addition is 5g/l, and the pH value changes into beyond 2.91, makes other identical samples, and compares the permanance under the damp heat test.
[embodiment A-6]
Change 14～18 hydrates of the aluminium sulphate among the embodiment 1 into aluminum chloride 6 hydrates (with the pure pharmaceutical worker's industry of light corporate system), addition is 5g/l, and the pH value changes into beyond 2.83, makes other identical samples, and compares the permanance under the damp heat test.
[embodiment A-7]
With average degree of polymerization is that ((KURARAY corporate system trade name: VF-XS) dipping 2 minutes in 40 ℃ warm water is applicable to that swelling handles that to set stretching ratio be 1.30 times for 2400 polyvinyl alcohol film.The film of handling through swelling flooded 2 minutes with 30 ℃ in the aqueous solution that contains iodine (pure chemical company system) 0.25g/l, potassium iodide (pure chemical company system) 17.7g/l, carried out the processing of iodine and iodide.With boric acid (Societa Chimica Larderellos.p.a. corporate system) concentration 28g/l, treatment temperature is handled 5 minutes to use for 30 ℃ with the film after the dyeing processing.The film that boric acid is handled through being suitable for was handled 5 minutes in the aqueous solution that contains 50 ℃ of 30.0g/l boric acid while stretching 5.0 times.Keep the tight state of handling the gained film through this boric acid, in the aqueous solution of adjusting with 50g/l potassium iodide and 3.5g/l citric acid (with the pure pharmaceutical worker's industry of light corporate system), handled for 15 seconds down in 30 ℃.This moment, pH value of aqueous solution was 1.51.To under 70 ℃, carry out 9 minutes dried with the film that the potassium iodide that contains citric acid is handled gained.The film of dried gained is used the polyethenol series bonding agent, and (Fuji Photo Film Co Ltd.'s system, trade name: TD-80U) lamination obtains Polarizer with tri cellulose acetate membrane through alkali treatment.
The Polarizer of gained is cut into 40mm * 40mm size, via bonding agent (Japanese chemical drug corporate system, trade name: PTR-3000) paste as test sample with the glass plate of thickness 1mm.
The sample of making is applicable to damp heat test.The condition of damp heat test is in the environment of 65 ℃ of temperature, relative humidity 93%, measure to place (432 hours) on the 18th preceding with after monomer transmitance and degree of polarization.
[embodiment A-8]
Change the addition of the citric acid among the embodiment 7 into 0.05g/l, the pH value changes into beyond 4.8, makes other identical samples, and compares the permanance under the damp heat test.
[embodiment A-9]
Change the citric acid among the embodiment 7 into acetic acid, the addition of acetic acid is 0.04g/l, and the pH value changes into beyond 5.1, makes other identical samples, and compares the permanance under the damp heat test.
[embodiment A-10]
Change the citric acid among the embodiment 7 into acetic acid, the addition of acetic acid is 3.0g/l, and the pH value changes into beyond 2.58, makes other identical samples, and compares the permanance under the damp heat test.
Comparative example 1
Aluminium sulphate 14～18 hydrates in not adding embodiment 1, make other identical samples, and compare the permanance of damp heat test.
Comparative examples A-2
The citric acid in not adding embodiment A-7, make other identical samples, and compare the permanance under the damp heat test.
Comparative examples A-3
In embodiment A-4,, the film with dyed processing gained keeps pH value 3.4 except containing in the aqueous solution of 50 ℃ of 30.0g/l boric acid, in-draw to 5.0 in 5 minutes times, keep the tight state of handling the gained film through boric acid, in the aqueous solution of adjusting with the 50g/l potassium iodide 30 ℃ handled for 15 seconds beyond, make other identical samples, and compare the permanance under the damp heat test.
The measurement result that changes at the transmitance of embodiment 1, A-2 to A-10, comparative example 1, A-2, A-3, degree of polarization is shown in Table A-1.
[Table A-1]
| Before the damp heat test | Behind 65 ℃ * 93%RH * 432Hour | The transmitance variable quantity | The degree of polarization variable quantity | |||
| Transmitance (%) | Degree of polarization (%) | Transmitance (%) | Degree of polarization (%) | |||
| Embodiment 1 | 43.72 | 99.95 | 44.71 | 98.50 | 0.99 | -1.45 |
| Embodiment A-2 | 43.92 | 99.88 | 44.51 | 99.18 | 0.59 | -0.70 |
| Embodiment A-3 | 43.67 | 99.94 | 44.13 | 99.68 | 0.46 | -0.26 |
| Embodiment A-4 | 43.78 | 99.93 | 44.32 | 99.54 | 0.54 | -0.39 |
| Embodiment A-5 | 43.34 | 99.93 | 44.01 | 98.48 | 0.67 | -1.45 |
| Embodiment A-6 | 43.45 | 99.95 | 43.88 | 98.58 | 0.43 | -1.37 |
| Embodiment A-7 | 43.68 | 99.93 | 43.91 | 99.6 | 0.23 | -0.33 |
| Embodiment A-8 | 43.7 | 99.96 | 44.91 | 98.38 | 1.21 | -1.58 |
| Embodiment A-9 | 43.56 | 99.95 | 44.61 | 98.5 | 1.05 | -1.45 |
| Embodiment A-10 | 43.5 | 99.95 | 43.81 | 99.41 | 0.31 | -0.54 |
| Comparative example 1 | 43.76 | 99.93 | 45.98 | 94.84 | 2.22 | -5.09 |
| Comparative examples A-2 | 43.76 | 99.95 | 45.82 | 95.54 | 2.06 | -4.41 |
| Comparative examples A-3 | 43.92 | 99.91 | 44.91 | 97.22 | 0.99 | -2.69 |
Learn by above embodiment, comparative example: make it contain crosslinking chemical in the polyvinyl alcohol resin film that contains iodine, iodide of the present invention, become the film that is applicable to stretch processing, acidic materials except the boric acid that contains 0.0001～5.0wt%, the pH value is in the light polarizing film of the solution-treated gained of 1.0≤pH＜6.0, for example become in hygrothermal environment, at the following nondiscoloration of 65 ℃ of temperature, relative humidity 93% and the less light polarizing film or the Polarizer of reduction of degree of polarization.Can obtain at the Polarizer of LCD with high permeability, high-contrast and the high humidity heat durability of light polarizing film.Comparing embodiment 4 and comparative example 3 are set at 1.0≤pH＜6.0 via the pH value with the halogenide treatment trough and can carry out more resultful processing as can be known in addition.
Claims (18)
1. light polarizing film, be after containing the polyvinyl alcohol resin film drawn processing of iodine, iodide, crosslinking chemical and/or anti-hydrated agent, obtain to contain the mineral acid that do not comprise boric acid or the solution-treated of its esters and/or organic acid 0.0001～5.0wt%, above-mentioned solution is called acid treatment solution again.
2. light polarizing film as claimed in claim 1, wherein, acid treatment is 2≤pH≤5 with the pH value of solution.
3. light polarizing film as claimed in claim 1, it is after the polyvinyl alcohol resin film drawn that contains iodine, iodide, crosslinking chemical and/or anti-hydrated agent is handled, and is that the acid treatment of 2.4≤pH＜6.0 obtains with solution-treated with the pH value again.
4. light polarizing film as claimed in claim 1 contains halogenide in containing the mineral acid that do not comprise boric acid or its esters and/or organic acid solution.
5. light polarizing film as claimed in claim 1 wherein, does not comprise that the mineral acid of boric acid or its esters are wantonly more than a kind or 2 kinds in aluminium sulphate, aluminum chloride, aluminium nitrate or the sulfuric acid.
6. light polarizing film as claimed in claim 1 or 2 wherein, does not comprise that the mineral acid of boric acid or its esters are aluminium sulphate.
7. as each described light polarizing film in the claim 1～6, wherein, organic acid is carboxylic acid and/or the 'alpha '-hydroxy acids more than a kind, and obtains by containing this organic acid solution-treated.
8. light polarizing film as claimed in claim 7, wherein, organic acid is wantonly more than a kind or a kind in citric acid, oxalic acid, malic acid, tartrate or the acetic acid, and obtains by containing this organic acid solution-treated.
9. as each described light polarizing film in the claim 1～8, wherein, the stretching ratio of the above-mentioned polyvinyl alcohol resin film after the stretching is 3～8 times before stretching.
10. as claim 1 or 9 described light polarizing film, wherein, employed crosslinking chemical and/or anti-hydrated agent are boric acid during stretch processing.
11. a Polarizer is provided with protective seam at the single or double as each described light polarizing film in the claim 1～8.
12. a liquid crystal indicator is characterized in that having Polarizer as claimed in claim 11.
13. the manufacture method of a light polarizing film is characterized in that being the acid treatment solution-treated of 2.4≤pH＜6.0 again with the pH value with after containing the polyvinyl alcohol resin film drawn processing of iodine, iodide, crosslinking chemical and/or anti-hydrated agent.
14. the manufacture method of a Polarizer; after it is characterized in that to contain the polyvinyl alcohol resin film drawn processing of iodine, iodide, crosslinking chemical and/or anti-hydrated agent; be the acid treatment solution-treated of 2.4≤pH＜6.0 again with the pH value, and protective seam be set at the single or double of the light polarizing film of gained.
15. the manufacture method of a light polarizing film is characterized in that being the acid treatment solution-treated of 2.2≤pH≤5 again with the pH value with after containing the polyvinyl alcohol resin film drawn processing of iodine, iodide, crosslinking chemical.
16. the manufacture method of a light polarizing film, after it is characterized in that to contain the polyvinyl alcohol resin film drawn processing of iodine, iodide, crosslinking chemical and/or anti-hydrated agent, to contain the mineral acid that do not comprise boric acid or the solution-treated of its esters and/or organic acid 0.0001～5.0wt%, above-mentioned solution is called acid treatment solution again.
17. the manufacture method of light polarizing film as claimed in claim 15, wherein, acid treatment solution is to contain the aqueous solution that is selected from least a acidic materials in sulfuric acid, hydrochloric acid, nitric acid, aluminium sulphate, aluminum chloride, aluminium nitrate, formic acid, citric acid, chloracetic acid, acetic acid, oxalic acid, malic acid and the tartrate.
18. as the manufacture method of claim 16 or 17 described light polarizing film, wherein, acid treatment is 2～5 with the pH value of solution.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2005066915 | 2005-03-10 | ||
| JP066915/2005 | 2005-03-10 | ||
| JP151797/2005 | 2005-05-25 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN101137917A true CN101137917A (en) | 2008-03-05 |
| CN100549738C CN100549738C (en) | 2009-10-14 |
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| CN104635292A (en) * | 2015-03-13 | 2015-05-20 | 京东方科技集团股份有限公司 | Polarizing plate and manufacturing method thereof and display screen |
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