KR20130045952A - 가교결합가능한 셀룰로즈 에스터 조성물 및 이로부터 형성된 필름 - Google Patents
가교결합가능한 셀룰로즈 에스터 조성물 및 이로부터 형성된 필름 Download PDFInfo
- Publication number
- KR20130045952A KR20130045952A KR1020137009618A KR20137009618A KR20130045952A KR 20130045952 A KR20130045952 A KR 20130045952A KR 1020137009618 A KR1020137009618 A KR 1020137009618A KR 20137009618 A KR20137009618 A KR 20137009618A KR 20130045952 A KR20130045952 A KR 20130045952A
- Authority
- KR
- South Korea
- Prior art keywords
- cellulose
- film
- group
- films
- acetate
- 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.)
- Ceased
Links
- 229920002678 cellulose Polymers 0.000 title claims abstract description 102
- 239000000203 mixture Substances 0.000 title claims abstract description 75
- 239000004971 Cross linker Substances 0.000 claims abstract description 56
- 239000001913 cellulose Substances 0.000 claims abstract description 50
- 230000003287 optical effect Effects 0.000 claims abstract description 24
- 229920006217 cellulose acetate butyrate Polymers 0.000 claims abstract description 22
- 230000001681 protective effect Effects 0.000 claims abstract description 16
- 229920002284 Cellulose triacetate Polymers 0.000 claims abstract description 15
- 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 claims abstract description 14
- 229920002301 cellulose acetate Polymers 0.000 claims abstract description 11
- 229920000623 Cellulose acetate phthalate Polymers 0.000 claims abstract description 4
- 229940081734 cellulose acetate phthalate Drugs 0.000 claims abstract description 4
- 238000000034 method Methods 0.000 claims description 70
- 229920008347 Cellulose acetate propionate Polymers 0.000 claims description 21
- 229920002134 Carboxymethyl cellulose Polymers 0.000 claims description 10
- 239000001768 carboxy methyl cellulose Substances 0.000 claims description 10
- 235000010948 carboxy methyl cellulose Nutrition 0.000 claims description 10
- 239000008112 carboxymethyl-cellulose Substances 0.000 claims description 10
- 150000002148 esters Chemical class 0.000 claims description 10
- 229920003086 cellulose ether Polymers 0.000 claims description 9
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 9
- DQEFEBPAPFSJLV-UHFFFAOYSA-N Cellulose propionate Chemical compound CCC(=O)OCC1OC(OC(=O)CC)C(OC(=O)CC)C(OC(=O)CC)C1OC1C(OC(=O)CC)C(OC(=O)CC)C(OC(=O)CC)C(COC(=O)CC)O1 DQEFEBPAPFSJLV-UHFFFAOYSA-N 0.000 claims description 8
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 8
- 239000000853 adhesive Substances 0.000 claims description 8
- 230000001070 adhesive effect Effects 0.000 claims description 8
- 229920006218 cellulose propionate Polymers 0.000 claims description 8
- 239000003431 cross linking reagent Substances 0.000 claims description 7
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 claims description 6
- 125000000217 alkyl group Chemical group 0.000 claims description 5
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Natural products CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 claims description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 4
- UGZICOVULPINFH-UHFFFAOYSA-N acetic acid;butanoic acid Chemical compound CC(O)=O.CCCC(O)=O UGZICOVULPINFH-UHFFFAOYSA-N 0.000 claims description 4
- 229920001727 cellulose butyrate Polymers 0.000 claims description 4
- 125000003700 epoxy group Chemical group 0.000 claims description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 3
- RBQYRDMVYCPWRG-UHFFFAOYSA-N acetic acid;butanedioic acid;butanoic acid Chemical compound CC(O)=O.CCCC(O)=O.OC(=O)CCC(O)=O RBQYRDMVYCPWRG-UHFFFAOYSA-N 0.000 claims description 3
- AVMNFQHJOOYCAP-UHFFFAOYSA-N acetic acid;propanoic acid Chemical compound CC(O)=O.CCC(O)=O AVMNFQHJOOYCAP-UHFFFAOYSA-N 0.000 claims description 3
- 239000002904 solvent Substances 0.000 abstract description 30
- 229920000877 Melamine resin Polymers 0.000 abstract description 24
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 abstract description 21
- 150000003918 triazines Chemical class 0.000 abstract description 2
- 235000010980 cellulose Nutrition 0.000 abstract 2
- GZVHEAJQGPRDLQ-UHFFFAOYSA-N 6-phenyl-1,3,5-triazine-2,4-diamine Chemical compound NC1=NC(N)=NC(C=2C=CC=CC=2)=N1 GZVHEAJQGPRDLQ-UHFFFAOYSA-N 0.000 abstract 1
- 239000010408 film Substances 0.000 description 248
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 48
- 239000007787 solid Substances 0.000 description 30
- 239000000243 solution Substances 0.000 description 29
- 239000011521 glass Substances 0.000 description 26
- 238000005266 casting Methods 0.000 description 25
- 238000001035 drying Methods 0.000 description 22
- 238000006467 substitution reaction Methods 0.000 description 22
- 229920000642 polymer Polymers 0.000 description 19
- 229920003270 Cymel® Polymers 0.000 description 18
- 239000013557 residual solvent Substances 0.000 description 17
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 15
- 239000012948 isocyanate Substances 0.000 description 14
- 150000002513 isocyanates Chemical class 0.000 description 14
- 238000002360 preparation method Methods 0.000 description 14
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 14
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 12
- 229920001747 Cellulose diacetate Polymers 0.000 description 11
- 239000002245 particle Substances 0.000 description 10
- 229910001220 stainless steel Inorganic materials 0.000 description 10
- 239000010935 stainless steel Substances 0.000 description 10
- 125000004063 butyryl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 9
- 150000001875 compounds Chemical class 0.000 description 9
- 239000000463 material Substances 0.000 description 9
- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 9
- 239000006096 absorbing agent Substances 0.000 description 8
- 239000003513 alkali Substances 0.000 description 8
- 239000003054 catalyst Substances 0.000 description 8
- 239000004973 liquid crystal related substance Substances 0.000 description 8
- 238000002156 mixing Methods 0.000 description 8
- 239000004014 plasticizer Substances 0.000 description 8
- 238000003756 stirring Methods 0.000 description 8
- 239000000654 additive Substances 0.000 description 7
- 125000004183 alkoxy alkyl group Chemical group 0.000 description 7
- 239000003795 chemical substances by application Substances 0.000 description 7
- 238000004132 cross linking Methods 0.000 description 7
- 238000010438 heat treatment Methods 0.000 description 7
- 239000004615 ingredient Substances 0.000 description 7
- 230000008569 process Effects 0.000 description 7
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- HKQOBOMRSSHSTC-UHFFFAOYSA-N cellulose acetate Chemical compound OC1C(O)C(O)C(CO)OC1OC1C(CO)OC(O)C(O)C1O.CC(=O)OCC1OC(OC(C)=O)C(OC(C)=O)C(OC(C)=O)C1OC1C(OC(C)=O)C(OC(C)=O)C(OC(C)=O)C(COC(C)=O)O1.CCC(=O)OCC1OC(OC(=O)CC)C(OC(=O)CC)C(OC(=O)CC)C1OC1C(OC(=O)CC)C(OC(=O)CC)C(OC(=O)CC)C(COC(=O)CC)O1 HKQOBOMRSSHSTC-UHFFFAOYSA-N 0.000 description 6
- 239000012456 homogeneous solution Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- -1 C 5 hydrocarbons Chemical class 0.000 description 5
- 230000000996 additive effect Effects 0.000 description 5
- 125000003545 alkoxy group Chemical group 0.000 description 5
- 230000003796 beauty Effects 0.000 description 5
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 5
- 230000006835 compression Effects 0.000 description 5
- 238000007906 compression Methods 0.000 description 5
- 230000007423 decrease Effects 0.000 description 5
- 238000004090 dissolution Methods 0.000 description 5
- 229930195733 hydrocarbon Natural products 0.000 description 5
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- 230000005855 radiation Effects 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical group OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- 230000005540 biological transmission Effects 0.000 description 4
- 230000008859 change Effects 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 239000006224 matting agent Substances 0.000 description 4
- 239000012788 optical film Substances 0.000 description 4
- 238000000935 solvent evaporation Methods 0.000 description 4
- 238000004804 winding Methods 0.000 description 4
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 230000003667 anti-reflective effect Effects 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 150000002170 ethers Chemical class 0.000 description 3
- 238000001704 evaporation Methods 0.000 description 3
- 238000011049 filling Methods 0.000 description 3
- 230000009477 glass transition Effects 0.000 description 3
- 150000002430 hydrocarbons Chemical class 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 229910052740 iodine Inorganic materials 0.000 description 3
- 239000011630 iodine Substances 0.000 description 3
- 230000014759 maintenance of location Effects 0.000 description 3
- 150000007974 melamines Chemical class 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 238000000807 solvent casting Methods 0.000 description 3
- AYEKOFBPNLCAJY-UHFFFAOYSA-O thiamine pyrophosphate Chemical compound CC1=C(CCOP(O)(=O)OP(O)(O)=O)SC=[N+]1CC1=CN=C(C)N=C1N AYEKOFBPNLCAJY-UHFFFAOYSA-O 0.000 description 3
- 238000012546 transfer Methods 0.000 description 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- FFWSICBKRCICMR-UHFFFAOYSA-N 5-methyl-2-hexanone Chemical compound CC(C)CCC(C)=O FFWSICBKRCICMR-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000005977 Ethylene Substances 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 2
- 239000004327 boric acid Substances 0.000 description 2
- 125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 239000000356 contaminant Substances 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 2
- XLLIQLLCWZCATF-UHFFFAOYSA-N ethylene glycol monomethyl ether acetate Natural products COCCOC(C)=O XLLIQLLCWZCATF-UHFFFAOYSA-N 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 238000004299 exfoliation Methods 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 239000010410 layer Substances 0.000 description 2
- TWNIBLMWSKIRAT-VFUOTHLCSA-N levoglucosan Chemical group O[C@@H]1[C@@H](O)[C@H](O)[C@H]2CO[C@@H]1O2 TWNIBLMWSKIRAT-VFUOTHLCSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- XNLICIUVMPYHGG-UHFFFAOYSA-N pentan-2-one Chemical compound CCCC(C)=O XNLICIUVMPYHGG-UHFFFAOYSA-N 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 229920000139 polyethylene terephthalate Polymers 0.000 description 2
- 239000005020 polyethylene terephthalate Substances 0.000 description 2
- 230000002028 premature Effects 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- ILJSQTXMGCGYMG-UHFFFAOYSA-N triacetic acid Chemical compound CC(=O)CC(=O)CC(O)=O ILJSQTXMGCGYMG-UHFFFAOYSA-N 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- BYEAHWXPCBROCE-UHFFFAOYSA-N 1,1,1,3,3,3-hexafluoropropan-2-ol Chemical compound FC(F)(F)C(O)C(F)(F)F BYEAHWXPCBROCE-UHFFFAOYSA-N 0.000 description 1
- MYWOJODOMFBVCB-UHFFFAOYSA-N 1,2,6-trimethylphenanthrene Chemical compound CC1=CC=C2C3=CC(C)=CC=C3C=CC2=C1C MYWOJODOMFBVCB-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- ARXJGSRGQADJSQ-UHFFFAOYSA-N 1-methoxypropan-2-ol Chemical compound COCC(C)O ARXJGSRGQADJSQ-UHFFFAOYSA-N 0.000 description 1
- PSQZJKGXDGNDFP-UHFFFAOYSA-N 2,2,3,3,3-pentafluoropropan-1-ol Chemical compound OCC(F)(F)C(F)(F)F PSQZJKGXDGNDFP-UHFFFAOYSA-N 0.000 description 1
- NBUKAOOFKZFCGD-UHFFFAOYSA-N 2,2,3,3-tetrafluoropropan-1-ol Chemical compound OCC(F)(F)C(F)F NBUKAOOFKZFCGD-UHFFFAOYSA-N 0.000 description 1
- VXQBJTKSVGFQOL-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethyl acetate Chemical compound CCCCOCCOCCOC(C)=O VXQBJTKSVGFQOL-UHFFFAOYSA-N 0.000 description 1
- FPZWZCWUIYYYBU-UHFFFAOYSA-N 2-(2-ethoxyethoxy)ethyl acetate Chemical compound CCOCCOCCOC(C)=O FPZWZCWUIYYYBU-UHFFFAOYSA-N 0.000 description 1
- JTXMVXSTHSMVQF-UHFFFAOYSA-N 2-acetyloxyethyl acetate Chemical compound CC(=O)OCCOC(C)=O JTXMVXSTHSMVQF-UHFFFAOYSA-N 0.000 description 1
- NQBXSWAWVZHKBZ-UHFFFAOYSA-N 2-butoxyethyl acetate Chemical compound CCCCOCCOC(C)=O NQBXSWAWVZHKBZ-UHFFFAOYSA-N 0.000 description 1
- 125000003504 2-oxazolinyl group Chemical group O1C(=NCC1)* 0.000 description 1
- KFZMGEQAYNKOFK-UHFFFAOYSA-N 2-propanol Substances CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- RHQDFWAXVIIEBN-UHFFFAOYSA-N Trifluoroethanol Chemical compound OCC(F)(F)F RHQDFWAXVIIEBN-UHFFFAOYSA-N 0.000 description 1
- DAKWPKUUDNSNPN-UHFFFAOYSA-N Trimethylolpropane triacrylate Chemical compound C=CC(=O)OCC(CC)(COC(=O)C=C)COC(=O)C=C DAKWPKUUDNSNPN-UHFFFAOYSA-N 0.000 description 1
- OKKRPWIIYQTPQF-UHFFFAOYSA-N Trimethylolpropane trimethacrylate Chemical compound CC(=C)C(=O)OCC(CC)(COC(=O)C(C)=C)COC(=O)C(C)=C OKKRPWIIYQTPQF-UHFFFAOYSA-N 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000003172 aldehyde group Chemical group 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 150000004703 alkoxides Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229940072049 amyl acetate Drugs 0.000 description 1
- PGMYKACGEOXYJE-UHFFFAOYSA-N anhydrous amyl acetate Natural products CCCCCOC(C)=O PGMYKACGEOXYJE-UHFFFAOYSA-N 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 125000003435 aroyl group Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 125000004065 butanoic acid ester group Chemical group 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- NLCKLZIHJQEMCU-UHFFFAOYSA-N cyano prop-2-enoate Chemical class C=CC(=O)OC#N NLCKLZIHJQEMCU-UHFFFAOYSA-N 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 230000009977 dual effect Effects 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- WBJINCZRORDGAQ-UHFFFAOYSA-N formic acid ethyl ester Natural products CCOC=O WBJINCZRORDGAQ-UHFFFAOYSA-N 0.000 description 1
- 229910021485 fumed silica Inorganic materials 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 238000005227 gel permeation chromatography Methods 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 239000012760 heat stabilizer Substances 0.000 description 1
- CATSNJVOTSVZJV-UHFFFAOYSA-N heptan-2-one Chemical compound CCCCCC(C)=O CATSNJVOTSVZJV-UHFFFAOYSA-N 0.000 description 1
- MNWFXJYAOYHMED-UHFFFAOYSA-M heptanoate Chemical compound CCCCCCC([O-])=O MNWFXJYAOYHMED-UHFFFAOYSA-M 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- OAKJQQAXSVQMHS-UHFFFAOYSA-N hydrazine group Chemical group NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- GJRQTCIYDGXPES-UHFFFAOYSA-N iso-butyl acetate Natural products CC(C)COC(C)=O GJRQTCIYDGXPES-UHFFFAOYSA-N 0.000 description 1
- FGKJLKRYENPLQH-UHFFFAOYSA-M isocaproate Chemical compound CC(C)CCC([O-])=O FGKJLKRYENPLQH-UHFFFAOYSA-M 0.000 description 1
- JMMWKPVZQRWMSS-UHFFFAOYSA-N isopropanol acetate Natural products CC(C)OC(C)=O JMMWKPVZQRWMSS-UHFFFAOYSA-N 0.000 description 1
- 229940011051 isopropyl acetate Drugs 0.000 description 1
- GWYFCOCPABKNJV-UHFFFAOYSA-N isovaleric acid Chemical compound CC(C)CC(O)=O GWYFCOCPABKNJV-UHFFFAOYSA-N 0.000 description 1
- OQAGVSWESNCJJT-UHFFFAOYSA-N isovaleric acid methyl ester Natural products COC(=O)CC(C)C OQAGVSWESNCJJT-UHFFFAOYSA-N 0.000 description 1
- 239000003550 marker Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
- MCSAJNNLRCFZED-UHFFFAOYSA-N nitroethane Chemical compound CC[N+]([O-])=O MCSAJNNLRCFZED-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920006267 polyester film Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- FBCQUCJYYPMKRO-UHFFFAOYSA-N prop-2-enyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC=C FBCQUCJYYPMKRO-UHFFFAOYSA-N 0.000 description 1
- QTECDUFMBMSHKR-UHFFFAOYSA-N prop-2-enyl prop-2-enoate Chemical compound C=CCOC(=O)C=C QTECDUFMBMSHKR-UHFFFAOYSA-N 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 125000001252 propanoic acid ester group Chemical group 0.000 description 1
- LLHKCFNBLRBOGN-UHFFFAOYSA-N propylene glycol methyl ether acetate Chemical compound COCC(C)OC(C)=O LLHKCFNBLRBOGN-UHFFFAOYSA-N 0.000 description 1
- 239000011241 protective layer Substances 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- LFQCEHFDDXELDD-UHFFFAOYSA-N tetramethyl orthosilicate Chemical compound CO[Si](OC)(OC)OC LFQCEHFDDXELDD-UHFFFAOYSA-N 0.000 description 1
- 238000002076 thermal analysis method Methods 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 238000002834 transmittance Methods 0.000 description 1
- XZZNDPSIHUTMOC-UHFFFAOYSA-N triphenyl phosphate Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)(=O)OC1=CC=CC=C1 XZZNDPSIHUTMOC-UHFFFAOYSA-N 0.000 description 1
- NLVXSWCKKBEXTG-UHFFFAOYSA-N vinylsulfonic acid Chemical compound OS(=O)(=O)C=C NLVXSWCKKBEXTG-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B15/00—Preparation of other cellulose derivatives or modified cellulose, e.g. complexes
- C08B15/005—Crosslinking of cellulose derivatives
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/18—Manufacture of films or sheets
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3467—Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
- C08K5/3477—Six-membered rings
- C08K5/3492—Triazines
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L1/00—Compositions of cellulose, modified cellulose or cellulose derivatives
- C08L1/08—Cellulose derivatives
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L1/00—Compositions of cellulose, modified cellulose or cellulose derivatives
- C08L1/08—Cellulose derivatives
- C08L1/10—Esters of organic acids, i.e. acylates
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L1/00—Compositions of cellulose, modified cellulose or cellulose derivatives
- C08L1/08—Cellulose derivatives
- C08L1/10—Esters of organic acids, i.e. acylates
- C08L1/12—Cellulose acetate
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L1/00—Compositions of cellulose, modified cellulose or cellulose derivatives
- C08L1/08—Cellulose derivatives
- C08L1/10—Esters of organic acids, i.e. acylates
- C08L1/14—Mixed esters, e.g. cellulose acetate-butyrate
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B5/00—Optical elements other than lenses
- G02B5/30—Polarising elements
- G02B5/3083—Birefringent or phase retarding elements
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B5/00—Optical elements other than lenses
- G02B5/30—Polarising elements
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T156/00—Adhesive bonding and miscellaneous chemical manufacture
- Y10T156/10—Methods of surface bonding and/or assembly therefor
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31855—Of addition polymer from unsaturated monomers
- Y10T428/3188—Next to cellulosic
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31855—Of addition polymer from unsaturated monomers
- Y10T428/31935—Ester, halide or nitrile of addition polymer
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31971—Of carbohydrate
Landscapes
- Chemical & Material Sciences (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Physics & Mathematics (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- General Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- Manufacturing & Machinery (AREA)
- Polarising Elements (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Laminated Bodies (AREA)
- Liquid Crystal (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US68480805P | 2005-05-26 | 2005-05-26 | |
| US60/684,808 | 2005-05-26 | ||
| PCT/US2006/020123 WO2006127834A2 (en) | 2005-05-26 | 2006-05-24 | Crosslinkable, cellulose ester compositions and films formed therefrom |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020077027306A Division KR101323545B1 (ko) | 2005-05-26 | 2006-05-24 | 가교결합가능한 셀룰로즈 에스터 조성물 및 이로부터형성된 필름 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR20130045952A true KR20130045952A (ko) | 2013-05-06 |
Family
ID=36869857
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020137009618A Ceased KR20130045952A (ko) | 2005-05-26 | 2006-05-24 | 가교결합가능한 셀룰로즈 에스터 조성물 및 이로부터 형성된 필름 |
| KR1020077027306A Expired - Fee Related KR101323545B1 (ko) | 2005-05-26 | 2006-05-24 | 가교결합가능한 셀룰로즈 에스터 조성물 및 이로부터형성된 필름 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020077027306A Expired - Fee Related KR101323545B1 (ko) | 2005-05-26 | 2006-05-24 | 가교결합가능한 셀룰로즈 에스터 조성물 및 이로부터형성된 필름 |
Country Status (7)
| Country | Link |
|---|---|
| US (2) | US8304086B2 (https=) |
| EP (2) | EP1883531B1 (https=) |
| JP (2) | JP4965563B2 (https=) |
| KR (2) | KR20130045952A (https=) |
| CN (2) | CN101184618B (https=) |
| TW (1) | TWI395773B (https=) |
| WO (1) | WO2006127834A2 (https=) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8304086B2 (en) * | 2005-05-26 | 2012-11-06 | Eastman Chemical Company | Crosslinkable, cellulose ester compositions and films formed therefrom |
| US8349921B2 (en) | 2007-08-24 | 2013-01-08 | Eastman Chemical Company | Mixed cellulose ester films having +C plate and −A plate optical properties |
| WO2009029220A1 (en) * | 2007-08-24 | 2009-03-05 | Eastman Chemical Company | Mixed cellulose esters having low bifringence and films made therefrom |
| US9068063B2 (en) | 2010-06-29 | 2015-06-30 | Eastman Chemical Company | Cellulose ester/elastomer compositions |
| US9273195B2 (en) | 2010-06-29 | 2016-03-01 | Eastman Chemical Company | Tires comprising cellulose ester/elastomer compositions |
| US9708474B2 (en) | 2011-12-07 | 2017-07-18 | Eastman Chemical Company | Cellulose esters in pneumatic tires |
| US9523794B2 (en) * | 2013-03-07 | 2016-12-20 | Konica Minolta, Inc. | Optical film of cellulose ester and cellulose ether for vertical alignment liquid crystal displays |
| KR20150143715A (ko) * | 2013-05-17 | 2015-12-23 | 코니카 미놀타 가부시키가이샤 | 편광판 및 그것을 구비한 표시 장치 |
| TWI529206B (zh) * | 2014-12-12 | 2016-04-11 | 財團法人紡織產業綜合研究所 | 酯化纖維素薄膜及其製備方法 |
| CN106279453B (zh) * | 2015-05-28 | 2019-12-10 | 易媛 | 交联的高分子化合物及其制备方法、水凝胶、水基压裂液和用途 |
| US10077342B2 (en) | 2016-01-21 | 2018-09-18 | Eastman Chemical Company | Elastomeric compositions comprising cellulose ester additives |
| KR20170123828A (ko) * | 2016-04-29 | 2017-11-09 | 동우 화인켐 주식회사 | 편광판 및 이를 포함하는 액정표시장치 |
| KR20180000577A (ko) * | 2016-06-23 | 2018-01-03 | 동우 화인켐 주식회사 | 편광판 및 이를 포함하는 액정표시장치 |
| JP7127327B2 (ja) * | 2018-03-29 | 2022-08-30 | 東ソー株式会社 | セルロース系樹脂組成物およびそれを用いた光学フィルム |
| US11384224B1 (en) * | 2018-10-05 | 2022-07-12 | Celanese International Corporation | Cellulose acetate film with optical properties |
Family Cites Families (40)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2196768A (en) | 1938-03-11 | 1940-04-09 | Eastman Kodak Co | Enteric coating |
| US3022287A (en) | 1960-01-13 | 1962-02-20 | Eastman Kodak Co | Method of preparing cellulose esters of trimellitic acid |
| US3833289A (en) | 1970-05-28 | 1974-09-03 | Polaroid Corp | Composite light-polarizing element |
| JPS5443725B2 (https=) | 1973-05-28 | 1979-12-21 | ||
| JPS5688440A (en) | 1979-12-21 | 1981-07-17 | Daicel Chem Ind Ltd | Noval cellulose acetate resin composition |
| JPS6246625A (ja) | 1985-08-26 | 1987-02-28 | Fuji Photo Film Co Ltd | セルロ−ストリアセテ−トフイルムの乾燥方法 |
| JPH01105738A (ja) | 1987-10-19 | 1989-04-24 | Sanyo Kokusaku Pulp Co Ltd | 耐擦傷性、耐薬品性、防眩性を付与したトリアセテートフィルム |
| US5219510A (en) | 1990-09-26 | 1993-06-15 | Eastman Kodak Company | Method of manufacture of cellulose ester film |
| JP3619591B2 (ja) | 1995-01-19 | 2005-02-09 | 富士写真フイルム株式会社 | セルロースアセテートフイルムの製造方法 |
| JP3619592B2 (ja) | 1995-01-19 | 2005-02-09 | 富士写真フイルム株式会社 | セルロースアセテート溶液およびその調製方法 |
| JP3712215B2 (ja) | 1995-01-19 | 2005-11-02 | 富士写真フイルム株式会社 | セルロースアセテート溶液、その調製方法およびセルロースアセテートフイルムの製造方法 |
| US5668273A (en) * | 1996-01-29 | 1997-09-16 | Eastman Chemical Company | Carboxyalkyl cellulose esters |
| US6200925B1 (en) | 1997-03-13 | 2001-03-13 | Eastman Chemical Company | Catalyst compositions for the polymerization of olefins |
| JPH1121379A (ja) | 1997-07-03 | 1999-01-26 | Konica Corp | セルローストリアセテート溶液、その調製方法及びセルローストリアセテートフィルムの製造方法 |
| CN1300383A (zh) | 1998-04-29 | 2001-06-20 | 部鲁尔科学公司 | 得自纤维素粘合剂的快速蚀刻、热固性抗反射涂料 |
| US5994530A (en) * | 1998-06-25 | 1999-11-30 | Eastman Chemical Corporation | Carboxyalkyl cellulose esters for use in aqueous pigment dispersions |
| JP2000352620A (ja) | 1999-03-31 | 2000-12-19 | Konica Corp | 光学フィルム、偏光板及び液晶表示装置 |
| JP4260332B2 (ja) * | 1999-03-31 | 2009-04-30 | 富士フイルム株式会社 | セルロースエステルフイルム用レターデーション上昇剤、セルロースエステルフイルム、光学補償シート、楕円偏光板および液晶表示装置 |
| US6559915B1 (en) | 1999-07-19 | 2003-05-06 | Fuji Photo Film Co., Ltd. | Optical films having matt property, films having a high transmittance, polarizing plates and liquid crystal display devices |
| JP4010081B2 (ja) * | 1999-08-18 | 2007-11-21 | コニカミノルタホールディングス株式会社 | セルロースエステル及びそれを用いる偏光板保護フィルム |
| US6712896B2 (en) | 2000-05-26 | 2004-03-30 | Konica Minolta Holdings, Inc. | Cellulose ester film, optical film, polarizing plate, optical compensation film and liquid crystal display |
| JP4686846B2 (ja) | 2000-11-07 | 2011-05-25 | コニカミノルタホールディングス株式会社 | 偏光板用保護フィルム及びそれを用いた偏光板並びに表示装置 |
| US6844033B2 (en) | 2001-03-01 | 2005-01-18 | Konica Corporation | Cellulose ester film, its manufacturing method, polarizing plate, and liquid crystal display |
| WO2002075373A1 (en) | 2001-03-21 | 2002-09-26 | Fuji Photo Film Co., Ltd. | Antireflection film, and image display device |
| JP2003128838A (ja) | 2001-10-23 | 2003-05-08 | Fuji Photo Film Co Ltd | セルロースアシレートドープ溶液およびそれを用いたセルロースアシレートフィルムの製造方法 |
| JP3822102B2 (ja) | 2001-12-27 | 2006-09-13 | 富士写真フイルム株式会社 | 光拡散フイルム、その製造方法、偏光板および液晶表示装置 |
| CN100376619C (zh) | 2002-02-01 | 2008-03-26 | 富士胶片株式会社 | 粘稠液的制备方法和三醋酸纤维素薄膜的制备方法 |
| JP4089328B2 (ja) * | 2002-02-07 | 2008-05-28 | コニカミノルタホールディングス株式会社 | 延伸セルロースエステルフィルム、延伸セルロースエステルフィルムの製造方法、楕円偏光板及び表示装置 |
| JP4317679B2 (ja) * | 2002-05-23 | 2009-08-19 | 富士フイルム株式会社 | 光学フィルム用レターデーション上昇剤、セルロースエステルフィルム、光学補償シート、楕円偏光板および液晶表示装置 |
| US7084945B2 (en) | 2002-07-12 | 2006-08-01 | Eastman Kodak Company | Compensator having particular sequence of films and crosslinked barrier layer |
| WO2004038477A1 (en) | 2002-10-24 | 2004-05-06 | Fuji Photo Film Co., Ltd. | Process for producing cellulose acylate film |
| JP2004244497A (ja) | 2003-02-13 | 2004-09-02 | Konica Minolta Holdings Inc | セルロースエステルフィルム、偏光板及び液晶表示装置 |
| US6782196B1 (en) | 2003-02-28 | 2004-08-24 | Valeo Electrical Systems, Inc. | Fluid heater with freeze protection |
| JP2004292558A (ja) | 2003-03-26 | 2004-10-21 | Konica Minolta Holdings Inc | セルロースエステルフィルムとその製造方法および偏光板保護フィルム |
| US20040206693A1 (en) * | 2003-04-16 | 2004-10-21 | John Charkoudian | Crosslinked cellulosic membrane |
| WO2004104121A1 (en) | 2003-05-16 | 2004-12-02 | Eastman Chemical Company | Crosslinkable coating systems containing carboxyalkylcellulose esters |
| JP4479175B2 (ja) | 2003-06-06 | 2010-06-09 | コニカミノルタオプト株式会社 | ハードコートフィルム、その製造方法、偏光板及び表示装置 |
| JP2005115341A (ja) * | 2003-09-16 | 2005-04-28 | Fuji Photo Film Co Ltd | 光学補償シート、偏光板及びそれを用いた液晶表示装置 |
| JP4330410B2 (ja) * | 2003-09-22 | 2009-09-16 | 富士フイルム株式会社 | セルロースフィルム、偏光板および液晶表示装置 |
| US8304086B2 (en) * | 2005-05-26 | 2012-11-06 | Eastman Chemical Company | Crosslinkable, cellulose ester compositions and films formed therefrom |
-
2006
- 2006-05-23 US US11/439,002 patent/US8304086B2/en not_active Expired - Fee Related
- 2006-05-24 CN CN2006800182817A patent/CN101184618B/zh not_active Expired - Fee Related
- 2006-05-24 KR KR1020137009618A patent/KR20130045952A/ko not_active Ceased
- 2006-05-24 EP EP20060760349 patent/EP1883531B1/en not_active Not-in-force
- 2006-05-24 WO PCT/US2006/020123 patent/WO2006127834A2/en not_active Ceased
- 2006-05-24 KR KR1020077027306A patent/KR101323545B1/ko not_active Expired - Fee Related
- 2006-05-24 CN CN201010173889A patent/CN101840016A/zh active Pending
- 2006-05-24 JP JP2008513682A patent/JP4965563B2/ja not_active Expired - Fee Related
- 2006-05-24 EP EP20100003617 patent/EP2196311A3/en not_active Withdrawn
- 2006-05-26 TW TW95118853A patent/TWI395773B/zh not_active IP Right Cessation
-
2012
- 2012-01-26 JP JP2012014286A patent/JP2012098752A/ja active Pending
- 2012-04-11 US US13/444,183 patent/US8449939B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| KR101323545B1 (ko) | 2013-10-29 |
| US8304086B2 (en) | 2012-11-06 |
| CN101840016A (zh) | 2010-09-22 |
| JP4965563B2 (ja) | 2012-07-04 |
| TW200704684A (en) | 2007-02-01 |
| EP1883531B1 (en) | 2014-03-12 |
| WO2006127834A2 (en) | 2006-11-30 |
| US20060286397A1 (en) | 2006-12-21 |
| TWI395773B (zh) | 2013-05-11 |
| EP1883531A2 (en) | 2008-02-06 |
| US20120222793A1 (en) | 2012-09-06 |
| CN101184618A (zh) | 2008-05-21 |
| US8449939B2 (en) | 2013-05-28 |
| JP2008546011A (ja) | 2008-12-18 |
| WO2006127834A3 (en) | 2007-06-07 |
| EP2196311A3 (en) | 2010-07-07 |
| JP2012098752A (ja) | 2012-05-24 |
| CN101184618B (zh) | 2012-09-05 |
| KR20080013930A (ko) | 2008-02-13 |
| EP2196311A2 (en) | 2010-06-16 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US8449939B2 (en) | Crosslinkable, cellulose ester compositions and films formed therefrom | |
| JP4337345B2 (ja) | 偏光板及びそれを用いた液晶表示装置 | |
| US8097188B2 (en) | Method of manufacturing optical film | |
| JP5677627B2 (ja) | 偏光板及び液晶表示装置 | |
| JP4906308B2 (ja) | ポリビニルアルコール系フィルム、およびその製造方法 | |
| KR101228650B1 (ko) | 광학 필름, 그의 제조 방법, 편광판 및 액정 표시 장치 | |
| CN101180351A (zh) | 酰化纤维素薄膜、以及使用它的偏振片、光学补偿薄膜和液晶显示装置 | |
| JP2002249599A (ja) | セルロースエステルフィルム及びその製造方法 | |
| CN1956835B (zh) | 纤维素酰化物薄膜及其制造方法 | |
| CN100572427C (zh) | 纤维素酰化物薄膜和纤维素酰化物颗粒的制造方法 | |
| KR101495236B1 (ko) | 광학 보상 필름의 제조 방법, 광학 보상 필름, 편광판, 및 액정 표시 장치 | |
| JP2003240948A (ja) | 光学フィルム、偏光板、光学フィルムロ−ル、光学フィルムを用いた表示装置、光学フィルムの製造方法 | |
| JP2006290929A (ja) | セルロースエステルフィルム、セルロースエステルフィルムの製造方法、偏光板及び液晶表示装置 | |
| KR20170054293A (ko) | 광학 필름 | |
| JP4587264B2 (ja) | 光学補償フィルム及びそれを用いた偏光板、液晶表示装置 | |
| JP2008145739A (ja) | 光学フィルム、その製造方法、偏光板及び液晶表示装置 | |
| JP2017223941A (ja) | 偏光膜用ポリビニルアルコール系フィルム、およびその製造方法、ならびに偏光膜 | |
| JP5251973B2 (ja) | 光学フィルム、偏光板 | |
| KR20170113041A (ko) | 위상차 필름, 편광판 및 액정 표시 장치 | |
| JP4665939B2 (ja) | 光学フィルムの製造方法 | |
| JP2008197656A (ja) | 光学フィルム、偏光板 | |
| JP2005173024A (ja) | セルロースエステルフィルム及びその製造方法 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A107 | Divisional application of patent | ||
| PA0104 | Divisional application for international application |
Comment text: Divisional Application for International Patent Patent event code: PA01041R01D Patent event date: 20130416 |
|
| PG1501 | Laying open of application | ||
| A201 | Request for examination | ||
| PA0201 | Request for examination |
Patent event code: PA02012R01D Patent event date: 20130510 Comment text: Request for Examination of Application |
|
| E902 | Notification of reason for refusal | ||
| PE0902 | Notice of grounds for rejection |
Comment text: Notification of reason for refusal Patent event date: 20130703 Patent event code: PE09021S01D |
|
| E601 | Decision to refuse application | ||
| PE0601 | Decision on rejection of patent |
Patent event date: 20140218 Comment text: Decision to Refuse Application Patent event code: PE06012S01D Patent event date: 20130703 Comment text: Notification of reason for refusal Patent event code: PE06011S01I |