KR100523083B1 - 저비중, 중굴절률 광학 렌즈용 수지 조성물 및 그를이용하여 제조한 광학렌즈 - Google Patents
저비중, 중굴절률 광학 렌즈용 수지 조성물 및 그를이용하여 제조한 광학렌즈 Download PDFInfo
- Publication number
- KR100523083B1 KR100523083B1 KR10-2003-0002432A KR20030002432A KR100523083B1 KR 100523083 B1 KR100523083 B1 KR 100523083B1 KR 20030002432 A KR20030002432 A KR 20030002432A KR 100523083 B1 KR100523083 B1 KR 100523083B1
- Authority
- KR
- South Korea
- Prior art keywords
- weight
- compound
- resin composition
- bisphenol
- aliphatic
- 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.)
- Expired - Fee Related
Links
- 230000003287 optical effect Effects 0.000 title claims abstract description 38
- 239000011342 resin composition Substances 0.000 title claims abstract description 33
- -1 diacrylate compound Chemical class 0.000 claims abstract description 38
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical group C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 claims abstract description 37
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims abstract description 25
- 230000005484 gravity Effects 0.000 claims abstract description 14
- 125000000524 functional group Chemical group 0.000 claims abstract description 13
- 150000007824 aliphatic compounds Chemical class 0.000 claims abstract description 12
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 12
- 239000004593 Epoxy Substances 0.000 claims abstract description 11
- 230000001588 bifunctional effect Effects 0.000 claims abstract description 9
- 150000001875 compounds Chemical class 0.000 claims abstract description 9
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 9
- 239000000203 mixture Substances 0.000 claims abstract description 9
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 4
- 239000001257 hydrogen Substances 0.000 claims abstract description 4
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical group ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 claims description 15
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical group [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 10
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 8
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 claims description 8
- 229920000642 polymer Polymers 0.000 claims description 7
- 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 claims description 6
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 claims description 5
- PRJNEUBECVAVAG-UHFFFAOYSA-N 1,3-bis(ethenyl)benzene Chemical compound C=CC1=CC=CC(C=C)=C1 PRJNEUBECVAVAG-UHFFFAOYSA-N 0.000 claims description 5
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 claims description 5
- 239000000126 substance Substances 0.000 claims description 5
- WEERVPDNCOGWJF-UHFFFAOYSA-N 1,4-bis(ethenyl)benzene Chemical compound C=CC1=CC=C(C=C)C=C1 WEERVPDNCOGWJF-UHFFFAOYSA-N 0.000 claims description 4
- VOBUAPTXJKMNCT-UHFFFAOYSA-N 1-prop-2-enoyloxyhexyl prop-2-enoate Chemical compound CCCCCC(OC(=O)C=C)OC(=O)C=C VOBUAPTXJKMNCT-UHFFFAOYSA-N 0.000 claims description 4
- QUZSUMLPWDHKCJ-UHFFFAOYSA-N bisphenol A dimethacrylate Chemical compound C1=CC(OC(=O)C(=C)C)=CC=C1C(C)(C)C1=CC=C(OC(=O)C(C)=C)C=C1 QUZSUMLPWDHKCJ-UHFFFAOYSA-N 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 4
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 3
- IBVPVTPPYGGAEL-UHFFFAOYSA-N 1,3-bis(prop-1-en-2-yl)benzene Chemical compound CC(=C)C1=CC=CC(C(C)=C)=C1 IBVPVTPPYGGAEL-UHFFFAOYSA-N 0.000 claims description 2
- 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 claims description 2
- FHLPGTXWCFQMIU-UHFFFAOYSA-N [4-[2-(4-prop-2-enoyloxyphenyl)propan-2-yl]phenyl] prop-2-enoate Chemical compound C=1C=C(OC(=O)C=C)C=CC=1C(C)(C)C1=CC=C(OC(=O)C=C)C=C1 FHLPGTXWCFQMIU-UHFFFAOYSA-N 0.000 claims description 2
- 230000000379 polymerizing effect Effects 0.000 claims description 2
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 claims description 2
- XENVCRGQTABGKY-ZHACJKMWSA-N chlorohydrin Chemical compound CC#CC#CC#CC#C\C=C\C(Cl)CO XENVCRGQTABGKY-ZHACJKMWSA-N 0.000 claims 1
- 238000004043 dyeing Methods 0.000 abstract description 12
- 239000004033 plastic Substances 0.000 description 22
- 229920003023 plastic Polymers 0.000 description 22
- 229940106691 bisphenol a Drugs 0.000 description 14
- 239000011521 glass Substances 0.000 description 11
- 229920005989 resin Polymers 0.000 description 10
- 239000011347 resin Substances 0.000 description 10
- 238000010521 absorption reaction Methods 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 6
- 238000001723 curing Methods 0.000 description 6
- 239000000178 monomer Substances 0.000 description 6
- 230000000704 physical effect Effects 0.000 description 6
- 238000011282 treatment Methods 0.000 description 6
- HWSSEYVMGDIFMH-UHFFFAOYSA-N 2-[2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOCCOC(=O)C(C)=C HWSSEYVMGDIFMH-UHFFFAOYSA-N 0.000 description 5
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 4
- JHQVCQDWGSXTFE-UHFFFAOYSA-N 2-(2-prop-2-enoxycarbonyloxyethoxy)ethyl prop-2-enyl carbonate Chemical compound C=CCOC(=O)OCCOCCOC(=O)OCC=C JHQVCQDWGSXTFE-UHFFFAOYSA-N 0.000 description 4
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 4
- 125000001931 aliphatic group Chemical group 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 238000004132 cross linking Methods 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 239000003505 polymerization initiator Substances 0.000 description 4
- 238000006116 polymerization reaction Methods 0.000 description 4
- 238000002834 transmittance Methods 0.000 description 4
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 230000008859 change Effects 0.000 description 3
- 238000007796 conventional method Methods 0.000 description 3
- 238000007334 copolymerization reaction Methods 0.000 description 3
- 125000004386 diacrylate group Chemical group 0.000 description 3
- QEBJRRFIWCWPMA-UHFFFAOYSA-N diethyl-bis(sulfanyl)-$l^{4}-sulfane Chemical compound CCS(S)(S)CC QEBJRRFIWCWPMA-UHFFFAOYSA-N 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000005498 polishing Methods 0.000 description 3
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
- FIHBHSQYSYVZQE-UHFFFAOYSA-N 6-prop-2-enoyloxyhexyl prop-2-enoate Chemical compound C=CC(=O)OCCCCCCOC(=O)C=C FIHBHSQYSYVZQE-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 102100026735 Coagulation factor VIII Human genes 0.000 description 2
- 101000911390 Homo sapiens Coagulation factor VIII Proteins 0.000 description 2
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 2
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical group CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 238000000137 annealing Methods 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000013329 compounding Methods 0.000 description 2
- VLXBWPOEOIIREY-UHFFFAOYSA-N dimethyl diselenide Natural products C[Se][Se]C VLXBWPOEOIIREY-UHFFFAOYSA-N 0.000 description 2
- WQOXQRCZOLPYPM-UHFFFAOYSA-N dimethyl disulfide Chemical compound CSSC WQOXQRCZOLPYPM-UHFFFAOYSA-N 0.000 description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 125000005843 halogen group Chemical group 0.000 description 2
- 150000002430 hydrocarbons Chemical group 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- ZDHCZVWCTKTBRY-UHFFFAOYSA-N omega-Hydroxydodecanoic acid Natural products OCCCCCCCCCCCC(O)=O ZDHCZVWCTKTBRY-UHFFFAOYSA-N 0.000 description 2
- 229920001451 polypropylene glycol Polymers 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 238000004383 yellowing Methods 0.000 description 2
- FVQMJJQUGGVLEP-UHFFFAOYSA-N (2-methylpropan-2-yl)oxy 2-ethylhexaneperoxoate Chemical compound CCCCC(CC)C(=O)OOOC(C)(C)C FVQMJJQUGGVLEP-UHFFFAOYSA-N 0.000 description 1
- 229920002818 (Hydroxyethyl)methacrylate Polymers 0.000 description 1
- DHBXNPKRAUYBTH-UHFFFAOYSA-N 1,1-ethanedithiol Chemical compound CC(S)S DHBXNPKRAUYBTH-UHFFFAOYSA-N 0.000 description 1
- TZJQCUDHKUWEFU-UHFFFAOYSA-N 2,2-dimethylpentanenitrile Chemical compound CCCC(C)(C)C#N TZJQCUDHKUWEFU-UHFFFAOYSA-N 0.000 description 1
- WYGWHHGCAGTUCH-UHFFFAOYSA-N 2-[(2-cyano-4-methylpentan-2-yl)diazenyl]-2,4-dimethylpentanenitrile Chemical compound CC(C)CC(C)(C#N)N=NC(C)(C#N)CC(C)C WYGWHHGCAGTUCH-UHFFFAOYSA-N 0.000 description 1
- LPUUPYOHXHWKAR-UHFFFAOYSA-N 2-ethyl-2-(hydroxymethyl)propane-1,3-diol 3,3,3-tris(sulfanyl)propanoic acid Chemical compound SC(CC(=O)O)(S)S.C(O)C(CC)(CO)CO LPUUPYOHXHWKAR-UHFFFAOYSA-N 0.000 description 1
- XMLYCEVDHLAQEL-UHFFFAOYSA-N 2-hydroxy-2-methyl-1-phenylpropan-1-one Chemical compound CC(C)(O)C(=O)C1=CC=CC=C1 XMLYCEVDHLAQEL-UHFFFAOYSA-N 0.000 description 1
- GZWIBBZCQMNKPK-UHFFFAOYSA-N 3-(3-sulfanylpropylsulfanyl)propane-1-thiol Chemical compound SCCCSCCCS GZWIBBZCQMNKPK-UHFFFAOYSA-N 0.000 description 1
- CAMBAGZYTIDFBK-UHFFFAOYSA-N 3-tert-butylperoxy-2-methylpropan-1-ol Chemical compound CC(CO)COOC(C)(C)C CAMBAGZYTIDFBK-UHFFFAOYSA-N 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- 229930185605 Bisphenol Natural products 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- MKYBYDHXWVHEJW-UHFFFAOYSA-N N-[1-oxo-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propan-2-yl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(C(C)NC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 MKYBYDHXWVHEJW-UHFFFAOYSA-N 0.000 description 1
- AFCARXCZXQIEQB-UHFFFAOYSA-N N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CCNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 AFCARXCZXQIEQB-UHFFFAOYSA-N 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- DJBDALSVJDXVPW-UHFFFAOYSA-N SCCC(=O)O.SCCC(=O)O.C(C)OCC Chemical compound SCCC(=O)O.SCCC(=O)O.C(C)OCC DJBDALSVJDXVPW-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 150000001253 acrylic acids Chemical class 0.000 description 1
- 229920006397 acrylic thermoplastic Polymers 0.000 description 1
- 239000002390 adhesive tape Substances 0.000 description 1
- 239000006117 anti-reflective coating Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 238000000149 argon plasma sintering Methods 0.000 description 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- SYFOAKAXGNMQAX-UHFFFAOYSA-N bis(prop-2-enyl) carbonate;2-(2-hydroxyethoxy)ethanol Chemical compound OCCOCCO.C=CCOC(=O)OCC=C SYFOAKAXGNMQAX-UHFFFAOYSA-N 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- VFHVQBAGLAREND-UHFFFAOYSA-N diphenylphosphoryl-(2,4,6-trimethylphenyl)methanone Chemical compound CC1=CC(C)=CC(C)=C1C(=O)P(=O)(C=1C=CC=CC=1)C1=CC=CC=C1 VFHVQBAGLAREND-UHFFFAOYSA-N 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- YLHXLHGIAMFFBU-UHFFFAOYSA-N methyl phenylglyoxalate Chemical compound COC(=O)C(=O)C1=CC=CC=C1 YLHXLHGIAMFFBU-UHFFFAOYSA-N 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- QYZFTMMPKCOTAN-UHFFFAOYSA-N n-[2-(2-hydroxyethylamino)ethyl]-2-[[1-[2-(2-hydroxyethylamino)ethylamino]-2-methyl-1-oxopropan-2-yl]diazenyl]-2-methylpropanamide Chemical compound OCCNCCNC(=O)C(C)(C)N=NC(C)(C)C(=O)NCCNCCO QYZFTMMPKCOTAN-UHFFFAOYSA-N 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- 229920006295 polythiol Polymers 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 230000002250 progressing effect Effects 0.000 description 1
- FZYCEURIEDTWNS-UHFFFAOYSA-N prop-1-en-2-ylbenzene Chemical compound CC(=C)C1=CC=CC=C1.CC(=C)C1=CC=CC=C1 FZYCEURIEDTWNS-UHFFFAOYSA-N 0.000 description 1
- KCTAWXVAICEBSD-UHFFFAOYSA-N prop-2-enoyloxy prop-2-eneperoxoate Chemical compound C=CC(=O)OOOC(=O)C=C KCTAWXVAICEBSD-UHFFFAOYSA-N 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- WTSBJMAOQNCZBF-UHFFFAOYSA-N sulfanylmethylsulfanylmethanethiol Chemical compound SCSCS WTSBJMAOQNCZBF-UHFFFAOYSA-N 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L63/00—Compositions of epoxy resins; Compositions of derivatives of epoxy resins
-
- 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
- C08K5/01—Hydrocarbons
-
- 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
- C08K5/04—Oxygen-containing compounds
- C08K5/09—Carboxylic acids; Metal salts thereof; Anhydrides thereof
-
- 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
- C08K5/04—Oxygen-containing compounds
- C08K5/10—Esters; Ether-esters
- C08K5/11—Esters; Ether-esters of acyclic polycarboxylic acids
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B1/00—Optical elements characterised by the material of which they are made; Optical coatings for optical elements
- G02B1/04—Optical elements characterised by the material of which they are made; Optical coatings for optical elements made of organic materials, e.g. plastics
- G02B1/041—Lenses
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Macromonomer-Based Addition Polymer (AREA)
Abstract
Description
원료명 | 실시예1 | 실시예2 | 실시예3 | 실시예4 | 비교예1 | 비교예2 |
BPA-Polymer | 20 | 45 | 42 | 47 | 56 | |
BP-2-EMA | 54 | |||||
BPA-4E-EDMA 또는 BP-2EA | 27 | |||||
TMPTMA | 5 | 15 | 10 | 5 | 9 | |
MMA | 15 | 15 | ||||
MAA | 15 | 20 | 10 | 15 | ||
SM | 10 | 15 | 10 | 5 | 5 | |
HDDA | 15 | 10 | 18 | 15 | 18 | |
TEGDMA | 8 | 10 | 5 | 13 | 9 | |
HEMA | 6 | |||||
a-MSD | 1 | |||||
DVB | 1.5 | |||||
DMDS(후첨) | 1 | 1 | 1 | 0.5 | ||
굴절률(n D 20) | 1.5510 | 1.5490 | 1.5538 | 1.5513 | 1.549 | 1.548 |
아베수(v D 20) | 40 | 42 | 40 | 40 | 41 | 40 |
비중(g/cm3) | 1.15 | 1.15 | 1.16 | 1.16 | 1.17 | 1.18 |
내충격성 | O | O | O | O | O | O |
내후성 | O | O | O | O | ⅹ | ⅹ |
염색성 | O | O | O | O | ⅹ | O |
내열성 | O | O | O | O | ⅹ | O |
광학왜곡 | O | O | O | O | O | ⅹ |
광투과률 | 93% | 93% | 92% | 93% | 89% | 85% |
UV차단 | 100% | 100% | 100% | 100% | 95% | 90% |
내용제성 | O | O | O | O | ⅹ | ⅹ |
Claims (7)
- (A) 하기 화학식 1로 표현되는 비스페놀 A 골격을 갖는 2작용성 이상의 에폭시디아크릴레이트 화합물 10 내지 50 중량%;[화학식 1](상기 식에서, R1은 메틸기이며, n은 2 내지 4의 정수이다.)(B) 하기 화학식 2로 표현되는 2작용성 이상의 비스페놀 A계 에폭시 디아크릴레이트 화합물 1 내지 30 중량%;[화학식 2](상기 식에서, R1은 메틸기이며, R2는 수소 또는 메틸기이고, n은 2 내지 5의 정수이다.)(C) 3개 이상의 아크릴 작용기를 가지는 지방족 화합물 0 내지 20중량%;(D) 메타크릴산 10 내지 30 중량%;(E) 1개 이상 작용기를 포함한 방향족 알릴화합물 0 내지 25중량%;(F) 2개 이상의 수산기와 2개 이상의 아크릴기를 가지는 지방족 화합물 5 내지 30중량%; 및(G) 2개 이상의 아크릴기를 가지는 지방족 메타아크릴레이트 화합물 5 내지 20중량%를 포함하는 저비중, 중굴절률 광학 렌즈용 수지 조성물.
- 제1항에 있어서, 상기 화학식 1로 표현되는 화합물은 클로로메틸옥시란 및 2-프로페노에이트가 결합된 4,4-(1-메틸에틸리덴)비스페놀 폴리머인 것인 광학 렌즈용 수지 조성물.
- 제1항에 있어서, 상기 화학식 2로 표현되는 화합물은 에피클로로히드린과 테트라에틸렌옥사이드가 첨가된 비스페놀 A 디메타크릴레이트, 에피클로로히드린과 디에틸렌옥사이드가 첨가된 비스페놀 A 디아크릴레이트, 에피클로로히드린과 데카에틸렌옥사이드가 첨가된 비스페놀 A 디메타크릴레이트 및 이들의 혼합물로 이루어진 군으로부터 선택되는 것인 광학 렌즈용 수지 조성물.
- 제1항에 있어서, 상기 (C) 3개 이상의 아크릴 작용기를 가지는 지방족 화합물은 트리메틸올프로판 트리메타아크릴레이트, 트리메틸올프로판 트리아크릴레이트, 트리에틸올프로판 트리메타아크릴레이트, 트리에틸올프로판 트리아크릴레이트 및 이들의 혼합물로 이루어진 군으로부터 선택되는 것인 광학 렌즈용 수지 조성물.
- 제1항에 있어서, 상기 (F) 2개 이상의 수산기와 2개 이상의 아크릴기를 가지는 지방족 화합물은 헥산디올디아크릴레이트이고, 상기 (G) 2개 이상의 아크릴기를 가지는 지방족 메타아크릴레이트 화합물은 트리에틸렌글리콜 디메타크릴레이트인 것인 광학 렌즈용 수지 조성물.
- 제1항에 있어서, 상기 (E) 방향족 알릴화합물은 스티렌, 알파메틸스티렌, 알파메틸스티렌다이머, o-디비닐벤젠, m-디비닐벤젠, p-디비닐벤젠, m-디이소프로페닐벤젠 및 이들의 혼합물로 이루어진 군으로부터 선택되는 것인 광학 렌즈용 수지 조성물.
- 제1항 내지 제5항 중 어느 한 항에 따른 광학 렌즈용 수지 조성물을 라디칼 중합하여 제조한 광학 렌즈.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR10-2003-0002432A KR100523083B1 (ko) | 2003-01-14 | 2003-01-14 | 저비중, 중굴절률 광학 렌즈용 수지 조성물 및 그를이용하여 제조한 광학렌즈 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR10-2003-0002432A KR100523083B1 (ko) | 2003-01-14 | 2003-01-14 | 저비중, 중굴절률 광학 렌즈용 수지 조성물 및 그를이용하여 제조한 광학렌즈 |
Publications (2)
Publication Number | Publication Date |
---|---|
KR20040065454A KR20040065454A (ko) | 2004-07-22 |
KR100523083B1 true KR100523083B1 (ko) | 2005-10-20 |
Family
ID=37355634
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR10-2003-0002432A Expired - Fee Related KR100523083B1 (ko) | 2003-01-14 | 2003-01-14 | 저비중, 중굴절률 광학 렌즈용 수지 조성물 및 그를이용하여 제조한 광학렌즈 |
Country Status (1)
Country | Link |
---|---|
KR (1) | KR100523083B1 (ko) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR101105423B1 (ko) * | 2008-01-08 | 2012-01-17 | 주식회사 엘지화학 | 광학 필름 및 이를 포함하는 정보전자 장치 |
US9168694B2 (en) | 2008-01-08 | 2015-10-27 | Lg Chem, Ltd. | Transparent resin composition |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100711624B1 (ko) | 2006-02-28 | 2007-05-02 | 주식회사 니드필 | 고굴절률 광학 렌즈용 수지 조성물 및 그를 이용하여제조한 광학 렌즈 |
KR102097174B1 (ko) * | 2012-08-27 | 2020-04-06 | 주식회사 케이오씨솔루션 | 저장 안정성이 향상된 에폭시 아크릴계 광학재료용 중합성 조성물 및 에폭시 아크릴계 광학재료의 제조방법 |
KR20180128296A (ko) * | 2017-05-23 | 2018-12-03 | 주식회사 케이오씨솔루션 | 에폭시 아크릴계 중굴절 광학렌즈용 수지 조성물 및 그 제조방법 |
KR101864265B1 (ko) * | 2017-05-25 | 2018-06-08 | 주식회사 케이오씨솔루션 | 에폭시 아크릴계 중굴절 광학렌즈용 수지 조성물 및 그 제조방법 |
KR101920164B1 (ko) * | 2017-09-05 | 2018-11-19 | 주식회사 케이오씨솔루션 | 에폭시 아크릴계 중굴절 광학렌즈용 수지 조성물 및 그 제조방법 |
-
2003
- 2003-01-14 KR KR10-2003-0002432A patent/KR100523083B1/ko not_active Expired - Fee Related
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR101105423B1 (ko) * | 2008-01-08 | 2012-01-17 | 주식회사 엘지화학 | 광학 필름 및 이를 포함하는 정보전자 장치 |
KR101127913B1 (ko) * | 2008-01-08 | 2012-04-20 | 주식회사 엘지화학 | 광학 필름 및 이를 포함하는 정보전자 장치 |
KR101336301B1 (ko) | 2008-01-08 | 2013-12-02 | 주식회사 엘지화학 | 광학 필름 및 이를 포함하는 정보전자 장치 |
US9168694B2 (en) | 2008-01-08 | 2015-10-27 | Lg Chem, Ltd. | Transparent resin composition |
Also Published As
Publication number | Publication date |
---|---|
KR20040065454A (ko) | 2004-07-22 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JPH11507087A (ja) | 高屈折率/高アッベ数組成物 | |
US6573348B2 (en) | Curable resin composition | |
KR20090034378A (ko) | 광학적 특성이 우수한 경화성 조성물 | |
KR100523083B1 (ko) | 저비중, 중굴절률 광학 렌즈용 수지 조성물 및 그를이용하여 제조한 광학렌즈 | |
JPH05194616A (ja) | プラスチックレンズのブルーイング方法 | |
KR100523077B1 (ko) | 고굴절률 광학 렌즈용 수지 조성물 및 그를 이용하여제조한 광학렌즈 | |
KR100529369B1 (ko) | 저비중, 중굴절률 광학 렌즈용 수지 조성물 및 그를이용하여 제조한 광학 렌즈 | |
JPH0931136A (ja) | プラスチックレンズ成形用組成物及びそれを用いたプラスチックレンズ | |
AU731071B2 (en) | Polymerizable monomer compositions, transparent polymer substrates, and optical and ophthalmic articles obtained | |
KR100474586B1 (ko) | 수지 조성물 및 그에 의해 제조된 광학 렌즈 | |
KR100819998B1 (ko) | 광변색성 수지, 이의 제조방법 및 광학제품 | |
JP2001124903A (ja) | 光硬化性樹脂製レンズ | |
JPH07206944A (ja) | プラスチックレンズ成形用組成物及びそれを用いたプラスチックレンズ | |
KR100849469B1 (ko) | 물리적, 화학적 특성이 우수한 렌즈용 수지 조성물 및 그를이용하여 제조한 광학 렌즈 | |
KR100477182B1 (ko) | 수지 조성물 및 그에 의해 제조된 광학 렌즈 | |
KR100711624B1 (ko) | 고굴절률 광학 렌즈용 수지 조성물 및 그를 이용하여제조한 광학 렌즈 | |
JPH08208776A (ja) | 樹脂組成物、レンズ用組成物及びその硬化物 | |
JP3363990B2 (ja) | プラスチックレンズ成形用組成物及びそれを用いたプラスチックレンズ | |
KR20020002342A (ko) | 저 비중, 고굴절률 광학 렌즈용 조성물 및 그 제조방법 | |
JPH08208775A (ja) | 樹脂組成物、レンズ用組成物及びその硬化物 | |
JPH11263811A (ja) | 光学的特性に優れた硬化性組成物及びそれからなるプラスチックレンズとその製法 | |
KR101452440B1 (ko) | 열안정성이 우수한 광학 렌즈용 수지 조성물 | |
JPH11158229A (ja) | 眼鏡レンズ用組成物および眼鏡レンズ | |
EP0938689A1 (en) | Uv-cured optical elements | |
JPH01309001A (ja) | プラスチックレンズ材料 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A201 | Request for examination | ||
PA0109 | Patent application |
Patent event code: PA01091R01D Comment text: Patent Application Patent event date: 20030114 |
|
PA0201 | Request for examination | ||
PG1501 | Laying open of application | ||
E902 | Notification of reason for refusal | ||
PE0902 | Notice of grounds for rejection |
Comment text: Notification of reason for refusal Patent event date: 20050316 Patent event code: PE09021S01D |
|
E701 | Decision to grant or registration of patent right | ||
PE0701 | Decision of registration |
Patent event code: PE07011S01D Comment text: Decision to Grant Registration Patent event date: 20050812 |
|
GRNT | Written decision to grant | ||
PR0701 | Registration of establishment |
Comment text: Registration of Establishment Patent event date: 20051013 Patent event code: PR07011E01D |
|
PR1002 | Payment of registration fee |
Payment date: 20051013 End annual number: 3 Start annual number: 1 |
|
PG1601 | Publication of registration | ||
PR1001 | Payment of annual fee |
Payment date: 20080724 Start annual number: 4 End annual number: 4 |
|
PR1001 | Payment of annual fee |
Payment date: 20091012 Start annual number: 5 End annual number: 5 |
|
PR1001 | Payment of annual fee |
Payment date: 20101005 Start annual number: 6 End annual number: 6 |
|
PR1001 | Payment of annual fee |
Payment date: 20111004 Start annual number: 7 End annual number: 7 |
|
FPAY | Annual fee payment |
Payment date: 20121008 Year of fee payment: 8 |
|
PR1001 | Payment of annual fee |
Payment date: 20121008 Start annual number: 8 End annual number: 8 |
|
FPAY | Annual fee payment |
Payment date: 20131010 Year of fee payment: 9 |
|
PR1001 | Payment of annual fee |
Payment date: 20131010 Start annual number: 9 End annual number: 9 |
|
FPAY | Annual fee payment |
Payment date: 20141008 Year of fee payment: 10 |
|
PR1001 | Payment of annual fee |
Payment date: 20141008 Start annual number: 10 End annual number: 10 |
|
FPAY | Annual fee payment |
Payment date: 20151013 Year of fee payment: 11 |
|
PR1001 | Payment of annual fee |
Payment date: 20151013 Start annual number: 11 End annual number: 11 |
|
LAPS | Lapse due to unpaid annual fee | ||
PC1903 | Unpaid annual fee |
Termination category: Default of registration fee Termination date: 20170723 |