KR100204260B1 - 방사선-경화성 매트릭스 물질, 이를 함유하는 광학 섬유 리본 및 상기 광학 섬유 리본의 제조 방법 - Google Patents
방사선-경화성 매트릭스 물질, 이를 함유하는 광학 섬유 리본 및 상기 광학 섬유 리본의 제조 방법 Download PDFInfo
- Publication number
- KR100204260B1 KR100204260B1 KR1019900009481A KR900009481A KR100204260B1 KR 100204260 B1 KR100204260 B1 KR 100204260B1 KR 1019900009481 A KR1019900009481 A KR 1019900009481A KR 900009481 A KR900009481 A KR 900009481A KR 100204260 B1 KR100204260 B1 KR 100204260B1
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- South Korea
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- acrylate
- coated
- cured
- Prior art date
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- Expired - Lifetime
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- 239000011159 matrix material Substances 0.000 title claims abstract description 119
- 239000013307 optical fiber Substances 0.000 title claims abstract description 77
- 238000004519 manufacturing process Methods 0.000 title abstract description 5
- 238000000576 coating method Methods 0.000 claims abstract description 51
- 239000011248 coating agent Substances 0.000 claims abstract description 42
- 239000000178 monomer Substances 0.000 claims abstract description 32
- UHESRSKEBRADOO-UHFFFAOYSA-N ethyl carbamate;prop-2-enoic acid Chemical compound OC(=O)C=C.CCOC(N)=O UHESRSKEBRADOO-UHFFFAOYSA-N 0.000 claims abstract description 30
- CERQOIWHTDAKMF-UHFFFAOYSA-M methacrylate group Chemical group C(C(=C)C)(=O)[O-] CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 claims abstract description 27
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims abstract description 24
- 125000001931 aliphatic group Chemical group 0.000 claims abstract description 21
- 239000004721 Polyphenylene oxide Substances 0.000 claims abstract description 20
- 229920000570 polyether Polymers 0.000 claims abstract description 20
- 239000000463 material Substances 0.000 claims abstract description 17
- 239000008199 coating composition Substances 0.000 claims abstract description 10
- 239000000203 mixture Substances 0.000 claims description 124
- 239000000835 fiber Substances 0.000 claims description 85
- 239000000976 ink Substances 0.000 claims description 27
- 239000002904 solvent Substances 0.000 claims description 24
- 238000000034 method Methods 0.000 claims description 21
- 239000007788 liquid Substances 0.000 claims description 17
- 239000003381 stabilizer Substances 0.000 claims description 12
- 125000000217 alkyl group Chemical group 0.000 claims description 11
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 9
- 229920000728 polyester Polymers 0.000 claims description 9
- 230000005855 radiation Effects 0.000 claims description 9
- 239000004215 Carbon black (E152) Substances 0.000 claims description 8
- 239000011521 glass Substances 0.000 claims description 8
- 229930195733 hydrocarbon Natural products 0.000 claims description 8
- 239000012790 adhesive layer Substances 0.000 claims description 7
- -1 when cured Substances 0.000 claims description 7
- 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 6
- ZNAAXKXXDQLJIX-UHFFFAOYSA-N bis(2-cyclohexyl-3-hydroxyphenyl)methanone Chemical class C1CCCCC1C=1C(O)=CC=CC=1C(=O)C1=CC=CC(O)=C1C1CCCCC1 ZNAAXKXXDQLJIX-UHFFFAOYSA-N 0.000 claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- 239000003086 colorant Substances 0.000 claims description 5
- 150000001875 compounds Chemical class 0.000 claims description 5
- 230000003287 optical effect Effects 0.000 claims description 5
- XMIIGOLPHOKFCH-UHFFFAOYSA-N 3-phenylpropionic acid Chemical compound OC(=O)CCC1=CC=CC=C1 XMIIGOLPHOKFCH-UHFFFAOYSA-N 0.000 claims description 4
- JTHZUSWLNCPZLX-UHFFFAOYSA-N 6-fluoro-3-methyl-2h-indazole Chemical compound FC1=CC=C2C(C)=NNC2=C1 JTHZUSWLNCPZLX-UHFFFAOYSA-N 0.000 claims description 4
- 239000003963 antioxidant agent Substances 0.000 claims description 4
- 238000004132 cross linking Methods 0.000 claims description 4
- UIYCHXAGWOYNNA-UHFFFAOYSA-N vinyl sulfide Chemical group C=CSC=C UIYCHXAGWOYNNA-UHFFFAOYSA-N 0.000 claims description 4
- MYWOJODOMFBVCB-UHFFFAOYSA-N 1,2,6-trimethylphenanthrene Chemical compound CC1=CC=C2C3=CC(C)=CC=C3C=CC2=C1C MYWOJODOMFBVCB-UHFFFAOYSA-N 0.000 claims description 3
- MTPIZGPBYCHTGQ-UHFFFAOYSA-N 2-[2,2-bis(2-prop-2-enoyloxyethoxymethyl)butoxy]ethyl prop-2-enoate Chemical compound C=CC(=O)OCCOCC(CC)(COCCOC(=O)C=C)COCCOC(=O)C=C MTPIZGPBYCHTGQ-UHFFFAOYSA-N 0.000 claims description 3
- RSROEZYGRKHVMN-UHFFFAOYSA-N 2-ethyl-2-(hydroxymethyl)propane-1,3-diol;oxirane Chemical compound C1CO1.CCC(CO)(CO)CO RSROEZYGRKHVMN-UHFFFAOYSA-N 0.000 claims description 3
- DMQYPVOQAARSNF-UHFFFAOYSA-N 3-[2,3-bis(3-prop-2-enoyloxypropoxy)propoxy]propyl prop-2-enoate Chemical compound C=CC(=O)OCCCOCC(OCCCOC(=O)C=C)COCCCOC(=O)C=C DMQYPVOQAARSNF-UHFFFAOYSA-N 0.000 claims description 3
- HVVWZTWDBSEWIH-UHFFFAOYSA-N [2-(hydroxymethyl)-3-prop-2-enoyloxy-2-(prop-2-enoyloxymethyl)propyl] prop-2-enoate Chemical compound C=CC(=O)OCC(CO)(COC(=O)C=C)COC(=O)C=C HVVWZTWDBSEWIH-UHFFFAOYSA-N 0.000 claims description 3
- 150000001412 amines Chemical class 0.000 claims description 3
- CDOSHBSSFJOMGT-UHFFFAOYSA-N linalool Chemical compound CC(C)=CCCC(C)(O)C=C CDOSHBSSFJOMGT-UHFFFAOYSA-N 0.000 claims description 3
- 150000002989 phenols Chemical class 0.000 claims description 3
- 150000003512 tertiary amines Chemical class 0.000 claims description 3
- PSGCQDPCAWOCSH-UHFFFAOYSA-N (4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl) prop-2-enoate Chemical compound C1CC2(C)C(OC(=O)C=C)CC1C2(C)C PSGCQDPCAWOCSH-UHFFFAOYSA-N 0.000 claims description 2
- MLKIVXXYTZKNMI-UHFFFAOYSA-N 1-(4-dodecylphenyl)-2-hydroxy-2-methylpropan-1-one Chemical compound CCCCCCCCCCCCC1=CC=C(C(=O)C(C)(C)O)C=C1 MLKIVXXYTZKNMI-UHFFFAOYSA-N 0.000 claims description 2
- OHQSQCACEXDHAJ-UHFFFAOYSA-N 2,2-di(butan-2-yloxy)-1-phenylethanone Chemical compound CCC(C)OC(OC(C)CC)C(=O)C1=CC=CC=C1 OHQSQCACEXDHAJ-UHFFFAOYSA-N 0.000 claims description 2
- GIMQKKFOOYOQGB-UHFFFAOYSA-N 2,2-diethoxy-1,2-diphenylethanone Chemical compound C=1C=CC=CC=1C(OCC)(OCC)C(=O)C1=CC=CC=C1 GIMQKKFOOYOQGB-UHFFFAOYSA-N 0.000 claims description 2
- PIZHFBODNLEQBL-UHFFFAOYSA-N 2,2-diethoxy-1-phenylethanone Chemical compound CCOC(OCC)C(=O)C1=CC=CC=C1 PIZHFBODNLEQBL-UHFFFAOYSA-N 0.000 claims description 2
- KWVGIHKZDCUPEU-UHFFFAOYSA-N 2,2-dimethoxy-2-phenylacetophenone Chemical compound C=1C=CC=CC=1C(OC)(OC)C(=O)C1=CC=CC=C1 KWVGIHKZDCUPEU-UHFFFAOYSA-N 0.000 claims description 2
- LZHUBCULTHIFNO-UHFFFAOYSA-N 2,4-dihydroxy-1,5-bis[4-(2-hydroxyethoxy)phenyl]-2,4-dimethylpentan-3-one Chemical compound C=1C=C(OCCO)C=CC=1CC(C)(O)C(=O)C(O)(C)CC1=CC=C(OCCO)C=C1 LZHUBCULTHIFNO-UHFFFAOYSA-N 0.000 claims description 2
- TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 claims description 2
- QPXVRLXJHPTCPW-UHFFFAOYSA-N 2-hydroxy-2-methyl-1-(4-propan-2-ylphenyl)propan-1-one Chemical compound CC(C)C1=CC=C(C(=O)C(C)(C)O)C=C1 QPXVRLXJHPTCPW-UHFFFAOYSA-N 0.000 claims description 2
- NQSLZEHVGKWKAY-UHFFFAOYSA-N 6-methylheptyl 2-methylprop-2-enoate Chemical compound CC(C)CCCCCOC(=O)C(C)=C NQSLZEHVGKWKAY-UHFFFAOYSA-N 0.000 claims description 2
- DXPPIEDUBFUSEZ-UHFFFAOYSA-N 6-methylheptyl prop-2-enoate Chemical compound CC(C)CCCCCOC(=O)C=C DXPPIEDUBFUSEZ-UHFFFAOYSA-N 0.000 claims description 2
- COCLLEMEIJQBAG-UHFFFAOYSA-N 8-methylnonyl 2-methylprop-2-enoate Chemical compound CC(C)CCCCCCCOC(=O)C(C)=C COCLLEMEIJQBAG-UHFFFAOYSA-N 0.000 claims description 2
- LVGFPWDANALGOY-UHFFFAOYSA-N 8-methylnonyl prop-2-enoate Chemical compound CC(C)CCCCCCCOC(=O)C=C LVGFPWDANALGOY-UHFFFAOYSA-N 0.000 claims description 2
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 claims description 2
- 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 2
- IAXXETNIOYFMLW-COPLHBTASA-N [(1s,3s,4s)-4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl] 2-methylprop-2-enoate Chemical compound C1C[C@]2(C)[C@@H](OC(=O)C(=C)C)C[C@H]1C2(C)C IAXXETNIOYFMLW-COPLHBTASA-N 0.000 claims description 2
- JUDXBRVLWDGRBC-UHFFFAOYSA-N [2-(hydroxymethyl)-3-(2-methylprop-2-enoyloxy)-2-(2-methylprop-2-enoyloxymethyl)propyl] 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC(CO)(COC(=O)C(C)=C)COC(=O)C(C)=C JUDXBRVLWDGRBC-UHFFFAOYSA-N 0.000 claims description 2
- INXWLSDYDXPENO-UHFFFAOYSA-N [2-(hydroxymethyl)-3-prop-2-enoyloxy-2-[[3-prop-2-enoyloxy-2,2-bis(prop-2-enoyloxymethyl)propoxy]methyl]propyl] prop-2-enoate Chemical compound C=CC(=O)OCC(COC(=O)C=C)(CO)COCC(COC(=O)C=C)(COC(=O)C=C)COC(=O)C=C INXWLSDYDXPENO-UHFFFAOYSA-N 0.000 claims description 2
- GTBGXKPAKVYEKJ-UHFFFAOYSA-N decyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCOC(=O)C(C)=C GTBGXKPAKVYEKJ-UHFFFAOYSA-N 0.000 claims description 2
- FWLDHHJLVGRRHD-UHFFFAOYSA-N decyl prop-2-enoate Chemical compound CCCCCCCCCCOC(=O)C=C FWLDHHJLVGRRHD-UHFFFAOYSA-N 0.000 claims description 2
- 125000004386 diacrylate group Chemical group 0.000 claims description 2
- GMSCBRSQMRDRCD-UHFFFAOYSA-N dodecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCOC(=O)C(C)=C GMSCBRSQMRDRCD-UHFFFAOYSA-N 0.000 claims description 2
- 229940119545 isobornyl methacrylate Drugs 0.000 claims description 2
- PBOSTUDLECTMNL-UHFFFAOYSA-N lauryl acrylate Chemical compound CCCCCCCCCCCCOC(=O)C=C PBOSTUDLECTMNL-UHFFFAOYSA-N 0.000 claims description 2
- 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 claims description 2
- HMZGPNHSPWNGEP-UHFFFAOYSA-N octadecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)C(C)=C HMZGPNHSPWNGEP-UHFFFAOYSA-N 0.000 claims description 2
- RZFODFPMOHAYIR-UHFFFAOYSA-N oxepan-2-one;prop-2-enoic acid Chemical compound OC(=O)C=C.O=C1CCCCCO1 RZFODFPMOHAYIR-UHFFFAOYSA-N 0.000 claims description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical class [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 claims description 2
- 229910052799 carbon Inorganic materials 0.000 claims 4
- 230000008961 swelling Effects 0.000 claims 3
- MQUMNTKHZXNYGW-UHFFFAOYSA-N 2-ethyl-2-(hydroxymethyl)propane-1,3-diol;propane-1,3-diol Chemical compound OCCCO.CCC(CO)(CO)CO MQUMNTKHZXNYGW-UHFFFAOYSA-N 0.000 claims 2
- NCNNNERURUGJAB-UHFFFAOYSA-N 3-[2,2-bis(3-prop-2-enoyloxypropoxymethyl)butoxy]propyl prop-2-enoate Chemical compound C=CC(=O)OCCCOCC(CC)(COCCCOC(=O)C=C)COCCCOC(=O)C=C NCNNNERURUGJAB-UHFFFAOYSA-N 0.000 claims 2
- HGDULKQRXBSKHL-UHFFFAOYSA-N 1,1-bis(2-methylprop-2-enoyloxy)propyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC(CC)(OC(=O)C(C)=C)OC(=O)C(C)=C HGDULKQRXBSKHL-UHFFFAOYSA-N 0.000 claims 1
- DNHNBMQCHKKDNI-UHFFFAOYSA-N 2-phenylbutan-1-ol Chemical compound CCC(CO)C1=CC=CC=C1 DNHNBMQCHKKDNI-UHFFFAOYSA-N 0.000 claims 1
- 241000283690 Bos taurus Species 0.000 claims 1
- 239000002657 fibrous material Substances 0.000 claims 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 claims 1
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 claims 1
- 125000005250 alkyl acrylate group Chemical group 0.000 abstract description 4
- 239000000758 substrate Substances 0.000 abstract 1
- 238000009472 formulation Methods 0.000 description 18
- 238000001723 curing Methods 0.000 description 13
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 8
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 7
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- 238000012360 testing method Methods 0.000 description 7
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- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- 238000010894 electron beam technology Methods 0.000 description 3
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- 230000007062 hydrolysis Effects 0.000 description 3
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- 239000000377 silicon dioxide Substances 0.000 description 3
- VFBJXXJYHWLXRM-UHFFFAOYSA-N 2-[2-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxy]ethylsulfanyl]ethyl 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)OCCSCCOC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 VFBJXXJYHWLXRM-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 206010041316 Solvent sensitivity Diseases 0.000 description 2
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- FSAJWMJJORKPKS-UHFFFAOYSA-N octadecyl prop-2-enoate Chemical class CCCCCCCCCCCCCCCCCCOC(=O)C=C FSAJWMJJORKPKS-UHFFFAOYSA-N 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
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- 230000008569 process Effects 0.000 description 2
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- 238000002411 thermogravimetry Methods 0.000 description 2
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- 238000004383 yellowing Methods 0.000 description 2
- QNODIIQQMGDSEF-UHFFFAOYSA-N (1-hydroxycyclohexyl)-phenylmethanone Chemical compound C=1C=CC=CC=1C(=O)C1(O)CCCCC1 QNODIIQQMGDSEF-UHFFFAOYSA-N 0.000 description 1
- KPWDGTGXUYRARH-UHFFFAOYSA-N 2,2,2-trichloroethanol Chemical compound OCC(Cl)(Cl)Cl KPWDGTGXUYRARH-UHFFFAOYSA-N 0.000 description 1
- FTALTLPZDVFJSS-UHFFFAOYSA-N 2-(2-ethoxyethoxy)ethyl prop-2-enoate Chemical compound CCOCCOCCOC(=O)C=C FTALTLPZDVFJSS-UHFFFAOYSA-N 0.000 description 1
- BFSVOASYOCHEOV-UHFFFAOYSA-N 2-diethylaminoethanol Chemical compound CCN(CC)CCO BFSVOASYOCHEOV-UHFFFAOYSA-N 0.000 description 1
- LXZMKGWDPDBHSO-UHFFFAOYSA-N 4-hydroxy-3-phenylbutan-2-one Chemical compound CC(=O)C(CO)C1=CC=CC=C1 LXZMKGWDPDBHSO-UHFFFAOYSA-N 0.000 description 1
- 229920002799 BoPET Polymers 0.000 description 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- BGYHLZZASRKEJE-UHFFFAOYSA-N [3-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxy]-2,2-bis[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxymethyl]propyl] 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)OCC(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 BGYHLZZASRKEJE-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
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- JZMPIUODFXBXSC-UHFFFAOYSA-N ethyl carbamate;prop-2-enoic acid Chemical compound OC(=O)C=C.OC(=O)C=C.CCOC(N)=O JZMPIUODFXBXSC-UHFFFAOYSA-N 0.000 description 1
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- YBMRDBCBODYGJE-UHFFFAOYSA-N germanium oxide Inorganic materials O=[Ge]=O YBMRDBCBODYGJE-UHFFFAOYSA-N 0.000 description 1
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 1
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Abstract
Description
Claims (16)
- (a) 지방족 폴리에테르-기재 우레탄 아크릴레이트 35 중량% - 98 중량%; (b) 다수의 아크릴레이트 또는 메타크릴레이트 부분을 갖는 단량체 0.5 중량% - 35 중량%; (c) C7-C18로 구성되는 알킬 부분을 갖는 아크릴레이트 또는 메타크릴레이트 단량체 0.5 중량% - 20 중량%; 및 (D) 광개시제 0 중량% - 10 중량% (상기 모든 백분율은 (a), (b), (c) 및 (d)의 총 중량을 기준으로 한 중량 %이다)로 구성되는 리본형상으로 코우팅처리되고 착색된 광학 섬유를 결합시키는 액상의 방사선-경화성 매트릭스 물질.
- 제1항에 있어서, (a), (b), (c) 및 (d) 만으로 구성되는 조성물에 비해 코우팅 처리되고 착색된 코우팅 광학 섬유에 대한 상기 매트릭스 물질의 접착력을 증가시킬 수 있는 성분 (e), 폴리에스테르 기재 지방족 우레탄 아크릴레이트 올리고머를 (a), (b), (c) 및 (d)의 총 중량을 기준으로 1 중량% - 30 중량% 포함하는 것을 특징으로 하는 방사선-경화성 매트릭스 물질.
- 제1항에 있어서, 삼차 아민; 힌더드 아민; 유기 아황산염; 힌더드 페놀; 항산화제 및 이들의 혼합물로 구성되는 군중에서 선택된 안정화제 (f)를, (a), (b), (c) 및 (d)의 총 중량을 기준으로 0.1 중량% - 3 중량% 포함하는 것을 특징으로 하는 방사선-경화성 매트릭스 물질.
- (a) 지방족 폴리에테르-기재 우레탄 아크릴레이트 35 중량% - 98 중량%; (b) 트리메틸올프로판 트리아크릴레이트 ; 트리메틸을 프로판 트리메타크릴레이트; 펜타에리트리톨 트리아크릴레이트; 펜타에리트리톨 프리메타크릴레이트; 펜타에리트리톨 테트라아크릴레이트; 펜타에리트리톨 테트라메타크릴레이트; 트리메틸올 프로판 프로폭실레이트 트리아크릴레이트; 트리메틸올프로판 프로폭실레이트 트리메타크릴레이트; 트리메틸올프로판 에톡실레이트 트리아크릴레이트; 트리메틸올프로판 에톡실레이트 트리메타크릴레이트, 글리세롤 프로폭시트리아크릴레이트; 글리세롤 프로폭시트리메타크릴레이트; 디펜타에리트리톨 모노히드록시 펜타아크릴레이트; 디펜타에리트리톨 모노히드록시 펜타메타크릴레이트; C6-C12탄화수소 디올 디아크릴레이트; C6-C12탄화수소디올 디메타크릴레이트; 및 이들의 혼합물로 구성되는 군중에서 선택되고, 다수의 아크릴레이트 또는 메타크릴레이트 부분을 갖는 단량체 0.5 중량% - 35 중량%; (c) 스테아릴 아크릴레이트; 스테아릴 메타크릴레이트; 이소옥틸 아크릴레이트; 이소옥틸 메타크릴레이트; 라우릴 아크릴레이트; 라우릴 메타크릴레이트; C14-C15탄화수소 디올 디아크릴레이트; C14-C15탄화수소 디올 디메타크릴레이트; 혹, 카프로락톤 아크릴레이트; 카프로락톤 메타크릴레이트; 데실 아크릴레이트; 데실 메타크릴레이트; 이소데실 아크릴레이트; 이소데실 메타크릴레이트; 이소보르닐 아크릴레이트; 이소보르닐 메타크릴레이트; 및 이들의 혼합물로 구성되는 군중에서 선택되고, C7-C18탄소 원자로 구성되는 알킬 부분을 갖는 아크릴레이트 또는 메타크릴레이트 단량체 0.5 중량% - 20 중량%; 및 (d) 히드록시시클로헥실페닐 케톤; 히드록시메틸 페닐 프로판은; 디메톡시페닐아세토페논; 2-메틸-1-[4-(메틸티오)페닐]-2-모르폴리노-프로판온-1; 1-(4-이소프로필페닐)-2-히드록시-2-메틸프로판-1-온; 4-(2-히드록시에톡시)페닐-(2-히드록시-2-프로필)케톤; 1-(4-도데실페닐)-2-히드록시-2-메틸프로판-1-온; 디에톡시아세토페논; 2,2-디-2차-부톡시아세토페논; 디에톡시-페닐아세토페논; 및 이들의 혼합물로 구성되는 군중에서 선택된 광개시제 0 중량% - 10 중량%; (상기 모든 백분율은 (a), (b), (c) 및 (d)의 총 중량을 기준으로한 중량%이다)로 구성되는, 리본형상으로 코우팅처리되고 착색된 광학 섬유를 결합시키는 방사선-경화성 매트릭스 물질.
- (a) 실리콘-개질 지방족 폴리에테르-기재 우레탄 아크릴레이트 64 중량% - 80 중량%; (b) 트리메틸올프로판 트리아크릴레이트 15 중량% - 21 중량%; (c) 스테아릴 아크릴레이트 3 중량% - 8 중량%; (d) 히드록시시클로헥실페닐 케톤 광기시제 2 중량% - 7 중량%; 및 (f) 티오디에틸렌 비스(3,5-디-삼차-부틸-4-히드록시)히드로 신나메이트 0.5 중량% - 1.5 중량%; (상기 모든 중량 백분율은 (a), (b), (c) 및 (d)의 총 중량을 기준으로 한 것임)로 구성되는, 리본형상으로 코우팅처리되고 착색 된 광학 섬유를 결합시키는 자외선-경화성 매트릭스 물질.
- 대개 평행인 배열로 광학 섬유를 기계적으로 배열하고; 제1항의 매트릭스 물질을 상기 섬유 주위에 적용시키고; 상기 매트릭스 물질을 경화시켜서 상기 배열로 상기 섬유를 고정시키는 것으로 구성되는 광학 섬유 리본의 제조 방법.
- 경화 아크릴레이트-함유 또는 경화 메타크릴레이트-함유 코우팅 조성물로 코우팅처리되고 그 코우팅상이 각기 다른 색의 개별 섬유 확인용 잉크로 착색된 유리 광학 섬유에, 제1항의 방사선-경화성 매트릭스 물질로 구성된, 경화된 방사선-경화가능한 매트릭스 물질의 접착층을 붙여서 경화된 매트릭스 물질을 상기 광학 섬유에 결합시키는 방법으로서, 접착층을 증가시킬 수 있는 성분을 비경화된 매트릭스 물질내로 혼입시키는 것으로 이루어지는 방법.
- (1) 코우팅처리된 광학 섬유 및 (2) (a) 전적으로 지방족 폴리에테르-기재 우레탄 아크릴레이트 35 중량% - 98 중량%; (b) 경화될 때 매트릭스 조성물을 가교결합시키고, 내용매성을 부여하고, 그리고 인장 탄성율을 증가시키기 위해, 단량체 분자당 다수의 아크릴레이트 또는 메타크릴레이트 부분을 갖는 단량체 충분한 양인 0.5 중량% - 35 중량%; (c) 매트릭스 조성물을 실질적으로 팽윤시키지 않고, 상기 매트릭스 조성물이 쉽게 벗겨질수 있도록 충분히 낮은 접착력을 갖는 사용 조건하에서 착색된 표면에 경화된 매트릭스 조성물이 접착되어 있도록 하기 위하여 C7-C18로 구성되는 알킬 부분을 갖는 모노아크릴레이트 또는 모노메타크릴레이트 단량체 충분한 양인 0.5 중량% - 20 중량%; 및 (d) 광개시제 0 중량% - 10 중량% (상기 모든 중량%는 (a), (b), (c) 및 (d)의 총중량을 기준으로 한 것임)로 구성되는, 조성물의 경화시 원하는 형상으로 다수의 코우팅처리된 광학 섬유를 끼워넣고 고정시키는 액상의 방사선-경화성 박리(release) 매트릭스 조성물로서, 상기 코우팅처리된 광학 섬유가 서로 원하는 관계로 배치되고, 상기 구조가 상기 코우팅처리된 광학 섬유를 상기 원하는 관계로 배열하고, 상기 액상의 매트릭스 조성물을 상기 코우팅처리된 광학 섬유에 적용하여 섬유내에 조성물을 끼워 넣은 다음, 경화시키도록 방사선을 노출시켜 상기 액상의 조성물을 경화시키으로써 생성되는, 상기 액상의 방사선-경화성 박리 매트릭스 조성물로 구성되며, 이때 상기 조성물이, 경화될 때, 상기 섬유로부터 상기 코우팅을 실질적으로 제거하지 않고 상기 코우팅 처리된 섬유상의 코우팅으로부터 벗겨질수 있고, 23±0.5℃에서 1000 psi 이상의 탄성율을 갖는, 광학 섬유 배열.
- 제8항에 있어서 (a), (b), (c) 및 (d) 만으로 구성되는 조성물에 비해 코우팅 처리되고 착색된 광학 섬유에 대한 상기 매트릭스 물질의 접착력을 향상시킬 수 있는 성분 (e), 폴리에스테르 기재 지방족 우레탄 아크릴레이트 올리고머를 (a), (b), (c) 및 (d)의 총 중량을 기준으로 1 중량% - 30 중량% 포함하는 것을 특징으로 하는 광학 섬유 배열.
- 제8항에 있어서, 삼차 아민; 힌더드 아민; 유기아황산염; 힌더드 페놀; 항산화제 및 이들의 혼합물로 구성되는 군중에서 선택된 안정화제 (f)를 (a), (b), (c) 및 (d)의 총 중량을 기준으로 0.1 중량% - 3 중량% 포함하는 것을 특징으로 하는 광학 섬유 배열.
- (1) 코우팅처리된 광학 섬유, 및 (2) (a) 전적으로 지방족 폴리에테르-기재 우레탄 아크릴레이트 53 중량% - 87.5 중량%; (b) 경화될 때 매트릭스 조성물을 가교결합시키고, 내용매성을 부여하고, 그리고 인장 탄성율을 증가시키기 위해, 단량체 분자당 다수의 아크릴레이트 또는 메타크릴레이트 부분을 가지며, 상기 부분이 트리메틸올프로판 트리아크릴레이트; 트리메틸올 프로판 트리메타크릴레이트; 펜타에리트리톨 트리아크릴레이트; 펜타에리트리톨 트리메타크릴레이트; 펜타에리트리톨 테트라아크릴레이트; 펜타에리트리톨 테트라메타크릴레이트; 트리메틸올프로판 프로폭실레이트 트리아크릴레이트; 트리메틸올프로판 프로폭실레이트 트리메타크릴레이트; 트리메틸올프로판 에톡실레이트 트리아크릴레이트; 트리메틸올프로판 에톡실레이트 트리메타크릴레이트, 글리세롤 프로폭시트리아크릴레이트; 글리세롤 프로폭시트리메타크릴레이트, 디펜타에리트리톨 노닐히드록시 펜타아크릴레이트; 티펜타에리트리톨 모노히드록시 펜타메타크릴레이트; C6-C12탄화수소디올 디아크릴레이트; C6-C12탄화수소 디올 디메타크릴레이트; 및 이들의 혼합물로 구성되는 군중에서 선택되는, 단량체의 충분한 양인 10 중량% - 25 중량%; (c) 매트릭스 조성물을 실질적으로 팽윤시키지 않고, 상기 매트릭스 조성물이 쉽게 벗겨질 수 있도록 하는 충분히 낮은 접착력을 갖는 사용 조건 하에서 착색된 표면에 경화된 매트릭스 조성물이 접착되어 있도록 하기 위하여 C7-C18로 구성되는 알킬 부분을 갖는 모노아크릴레이트 또는 모노메타크릴레이트 단량체 충분한 양인 1.0 중량% - 14 중량%; (d) 광개시제 1.5 중량% - 8 중량%; (e) (a), (b), (c) 및 (d) 만으로 구성되는 조성물에 비해 코우팅처리되고 착색된 광학 섬유에 대한 상기 매트릭스 물질의 접착력을 증가시킬 수 있는 성분 10 중량% - 30 중량% ; 및 (f) 안정화제 0.25 중량% - 2 중량% (상기 모든 중량%는 (a), (b), (c) 및 (d)의 총중량을 기준으로 한 것임)로 구성되는, 조성물의 경화시 원하는 형상으로 다수의 코우팅처리된 광학 섬유를 끼워넣고 고정시키는 액상의 방사선-경화성 박리 매트릭스 조성물로서, 상기 코우팅처리된 광학 섬유가 서로 원하는 관계로 배치된 다음, 상기 액상의 매트릭스 조성물을 상기 코우팅처리된 광학 섬유에 적용하여 섬유내에 조성물을 끼워 넣은 다음, 경화시키도록 방사선을 노출시켜 상기 액상의 조성믈울 경화시키는, 상기 액상의 자외성-경화성 매트릭스 조성물로 구성되며, 이때 상기 조성물이, 경화될 때, 상기 섬유로부터 상기 코우팅을 실질적으로 제거하지 않고 상기 코우팅 처리된 섬유상의 코우팅으로부터 벗겨질수 있고, 23±0.5℃에서 1000 psi 이상의 탄성율을 갖는, 광학 섬유배열.
- (1) 코우팅 처리된 광학 섬유, 및 (2) (a) 실리콘-개질된 전적으로 지방족인 폴리에테르-기재 우레탄 아크릴레이트 64 중량% - 80 중량% ; (b) 경화될 때 매트릭스 조성물을 가교결합시키고, 내용매성을 부여 하고, 그리고 인장탄성율을 증가시키기 위한, 트리메틸올프로판 트리아크릴레이트 충분한 양인 15 중량% - 21 중량%; (c) 매트릭스 조성물을 실질적으로 팽윤시키지 않고, 상기 매트릭스 조성물이 쉽게 벗겨질 수 있도록 하는 충분히 낮은 접착력을 갖는 사용 조건하에서 착색된 표면에 경화된 매트릭스 조성물이 접착되어 있도록 하기 위한 스테아릴 아크릴레이트 충분한 양인 3 중량% - 8 중량%; (d) 히드록시시클로헥실페닐 케톤 광개시제 2 중량% - 7 중량% ; 및 (f) 티오디에틸렌 비스(3,5-디-삼차-부틸-4-히드록시)히드로신나메이트 0.5 중량% - 1.5 중량%; (상기 모든 중량%는 (a), (b), (c) 및 (d)의 총 중량을 기준으로 한것임)로 구성되는, 조성물의 경화시 원하는 형상으로 다수의 코우팅처리된 광학 섬유를 끼워넣고 고정시키는 액상의 자외선-경화성 매트릭스 조성물로 구성되며, 이때, 상기 조성물이 경화될 때, 상기 섬유로부터 상기 코우팅을 실질적으로 제거하지 않고 상기 코우팅 처리된 섬유상의 코우팅으로부터 벗겨질 수 있고 23±0.5℃에서 1000 psi 이상의 탄성율을 갖는, 광학 섬유 배열.
- 섬유가 고정관계로 고착되는 배열로 배치되는 다수의 공학 섬유; 및 상기 배열로 상기 섬유들을 결합하는 방사선 경화성 매트릭스 물질로 구성되며, 이때 상기 매트릭스 물질이 사용 중에 상기 섬유를 물질에 부착시키도록 하지만 물질로부터 쉽게 벗겨질 수 있는 충분한 접착력을 갖는, 광학섬유 배열.
- 일반적으로 평행한 배열로 배치된 다수의 유리 광학 섬유; 및 상기 배열로 상기 섬유들을 결합하고, 하기 (a)-(e)로 구성되는 자외선-경화성 매트릭스 물질로 구성되는 광학 섬유 리본 조립체: (a) 실리콘-개질 지방족 폴리에테르-기재 우레탄 아크릴레이트 64 중량% - 80 중량% ; (b) 트리메틸올프로판 트리아크릴레이트 15 중량% - 21 중량%; (c) 히드록시시클로헥실페닐 케톤 광개시제 2 중량% - 7 중량%; 및 (f) 티오디에틸렌 비스(3,5-디-삼차-부틸-4-히드록시) 히드로신나메이트 0.5 중량% - 1.5 중량%; (상기 모든 중량%는 (a), (b), (c) 및 (d)의 총 중량을 기준으로 한것임).
- (1) 코우팅 처리된 광학 지지체, 및 (2) (a) 전적으로 지방족 폴리에테르-기재 우레탄 아크릴레이트 35 중량% - 98 중량%; (b) 경화될 때 매트릭스 조성물을 가교결합시키고, 내용매성을 부여하고, 그리고 인장 탄성율을 증가시키기 위해, 단량체 분자당 다수의 아크릴레이트 또는 메타크릴레이트 부분을 갖는 단량체 0.5 중량% - 35 중량% ; (c) 매트릭스 조성물을 실질적으로 팽윤시키지 않고, 상기 매트릭스 조성물이 쉽게 벗겨질수 있도록 하는 충분히 낮은 접착력을 갖는 사용 조건하에서 상기 표면에 경화된 매트릭스 조성물이 접착되어 있도록 하기 위해 C7-C18로 구성되는 알킬 부분을 갖는 모노아크릴레이트 또는 모노메타크릴레이트 단량체 충분한 양인 0.5 중량% - 20 중량%; 및 (d) 광개시제 0 중량% - 10 중량% (상기 모든 중량%는 (a), (b), (c) 및 (d)의 총중량을 기준으로 한 것임)로 구성되며, 박리 코우팅이 상기 표면상의 코우팅을 실질적으로 손상시키지 않고 상기 표면으로부터 벗겨질 수 있는, 지지체의 코우팅 처리된 표면에 대한 접착과 그 위의 적용을 위한 액상의 방사선-경화성 박리 매트릭스 코우팅 조성물로 구성되는 광학 섬유 배열.
- (1) 코우팅 처리된 광학 섬유, 및 (2) (A) 전적으로 지방족 폴리에테르-기재 우레탄 아크릴레이트 28 중량% - 98 중량%; (B) 경화될 때 매트릭스 조성물을 가교결합시키고, 내용매성을 부여하고, 그리고 인장 탄성율을 증가시키기 위해, 단량체 분자당 다수의 아크릴레이트 또는 메타크릴레이트 부분을 갖는 단량체 충분한 양인 0.4 중량% - 35 중량% ; (C) 광개시제 0 중량% - 10 중량% (상기 모든 중량%는 (A), (B) 및 (C)의 총중량을 기준으로 한 것임)로 구성되는, 조성물의 경화시 원하는 형상 으로 다수의 코우팅처리된 광학 섬유를 끼워넣고 고정시키는 액상의 방사선-경화성 박리 매트릭스 조성물로서, 상기 코우팅처리된 광학 섬유가 서로 원하는 관계로 배치되어 단일 구조를 형성하고, 상기 구조가 상기 코우팅 처리된 광학 섬유를 상기 원하는 관계로 배열하고, 상기 액상의 매트릭스 조성물을 상기 코우팅처리된 광학 섬유에 적용하여 섬유내에 조성물을 끼워 넣은 다음, 경화시키도록 방사선을 노출시켜 상기 액상의 조성물을 경화시킴으로써 생성되는, 상기 액상의 방사선-경화성 박리 매트릭스 조성물로 구성되며, 이때 상기 조성물이, 경화될 때, 상기 섬유로부터 상기 코우팅을 실질적으로 제거하지 않고 상기 코우팅 처리된 섬유상의 코우팅으로부터 벗겨질수 있고, 23±0.5℃에서 1000 psi 이상의 탄성율을 갖는, 광학 섬유 배열.
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100571475B1 (ko) * | 2002-05-13 | 2006-04-17 | 주식회사 루밴틱스 | 광섬유 리본 코팅용 난연성 수지 조성물 |
Families Citing this family (82)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA1341128C (en) | 1989-06-27 | 2000-10-24 | Borden Chemical, Inc. | Optical fiber array |
JP2883988B2 (ja) * | 1989-12-27 | 1999-04-19 | ジェイエスアール株式会社 | 液状硬化性樹脂組成物 |
FR2695394B1 (fr) * | 1992-09-07 | 1994-10-07 | Alcatel Cable | Résine polymère pour ruban à fibres optiques. |
US5285513A (en) * | 1992-11-30 | 1994-02-08 | At&T Bell Laboratories | Optical fiber cable provided with stabilized waterblocking material |
CA2129397C (en) * | 1993-12-21 | 2005-03-22 | Mujibar M. Rahman | Process for manufacturing optical fiber ribbons |
US6240230B1 (en) | 1997-03-06 | 2001-05-29 | Dsm N.V. | Protective materials for optical fibers which do not substantially discolor |
WO1997009648A1 (en) * | 1995-09-07 | 1997-03-13 | Dsm N.V. | Optical glass fiber ribbon assembly and radiation curable matrix forming composition |
US6052503A (en) * | 1995-09-07 | 2000-04-18 | Dsm N.V. | Optical glass fiber ribbon assembly and radiation curable matrix forming composition |
DE19535934C2 (de) * | 1995-09-27 | 2002-11-07 | Basf Coatings Ag | Haftfähiger Lackfilm |
CA2237393A1 (en) * | 1995-11-13 | 1997-05-22 | Alvin C. Levy | Matrix compounds for forming optical fiber ribbons |
JPH09143233A (ja) * | 1995-11-28 | 1997-06-03 | Japan Synthetic Rubber Co Ltd | 光硬化性液状樹脂組成物 |
US5908873A (en) * | 1995-12-20 | 1999-06-01 | Borden Chemicals, Inc. | Peelable bonded ribbon matrix material; optical fiber bonded ribbon arrays containing same; and process for preparing said optical fiber bonded ribbon arrays |
JP3715021B2 (ja) * | 1996-04-09 | 2005-11-09 | Jsr株式会社 | 液状硬化性樹脂組成物 |
US5933559A (en) * | 1996-07-22 | 1999-08-03 | Dsm N.V. | Radiation-curable cross-linked ribbon matrix material for bonding an array of coated optical glass fibers |
DE69736297T2 (de) | 1996-11-08 | 2007-07-26 | Dsm Ip Assets B.V. | Strahlungshärtbare optische glasfaserbeschichtungszusammensetzungen, beschichtete optische glasfasern und optische glasfaserzusammenstellungen |
JP3746871B2 (ja) * | 1997-04-14 | 2006-02-15 | Jsr株式会社 | 液状硬化性樹脂組成物 |
US6130980A (en) * | 1997-05-06 | 2000-10-10 | Dsm N.V. | Ribbon assemblies and ink coating compositions for use in forming the ribbon assemblies |
US6197422B1 (en) | 1997-05-06 | 2001-03-06 | Dsm, N.V. | Ribbon assemblies and radiation-curable ink compositions for use in forming the ribbon assemblies |
US6023547A (en) * | 1997-06-09 | 2000-02-08 | Dsm N.V. | Radiation curable composition comprising a urethane oligomer having a polyester backbone |
US6085010A (en) * | 1997-06-11 | 2000-07-04 | Dsm N.V. | Optical glass fiber ribbon assemblies and radiation-curable compositions for use in forming ribbon assemblies |
US6301415B1 (en) | 1997-08-14 | 2001-10-09 | Dsm N.V | Optical glass fiber ribbon assemblies, matrix forming compositions radiation-curable compositions |
WO1999052958A1 (en) * | 1998-04-15 | 1999-10-21 | Dsm N.V. | Radiation curable resin composition |
US6579618B1 (en) | 1997-08-15 | 2003-06-17 | Dsm N.V. | Coated optical fiber and radiation curable resin composition |
JPH11106448A (ja) * | 1997-10-07 | 1999-04-20 | Jsr Corp | 液状硬化性樹脂組成物およびその硬化物 |
US6048911A (en) * | 1997-12-12 | 2000-04-11 | Borden Chemical, Inc. | Coated optical fibers |
US6391936B1 (en) | 1997-12-22 | 2002-05-21 | Dsm N.V. | Radiation-curable oligomers radiation-curable compositions, coated optical glass fibers, and ribbon assemblies |
US6175677B1 (en) | 1998-04-17 | 2001-01-16 | Alcatel | Optical fiber multi-ribbon and method for making the same |
US6110593A (en) * | 1998-05-21 | 2000-08-29 | Dsm N.V. | Radiation-curable optical fiber primary coating system |
US6040357A (en) * | 1998-05-28 | 2000-03-21 | Dsm N.V. | Method of making a radiation-curable ink composition, radiation-curable ink composition and ribbon assembly |
US6253013B1 (en) * | 1999-03-29 | 2001-06-26 | Siecor Operations, Llc | Optical fiber arrays |
CA2333368A1 (en) | 1999-04-01 | 2000-10-12 | Patrick Vaughn | Optical fiber ribbons containing radiation cured encapsulating materials |
KR100483980B1 (ko) | 1999-08-09 | 2005-04-18 | 보던 케미칼 인코포레이티드 | 열 박리가능한 광섬유 리본 |
KR20010037679A (ko) * | 1999-10-19 | 2001-05-15 | 오주언 | 광섬유 리본 제조용 수지 조성물 및 이를 이용한 광섬유 리본 제조용 수지의 제조방법 |
DE19961402A1 (de) * | 1999-12-20 | 2001-07-05 | Basf Coatings Ag | Verfahren zur Herstellung von Beschichtungen aus thermisch und mit aktinischer Strahlung härtbaren Beschichtungstoffen |
AU1582701A (en) | 1999-12-30 | 2001-07-16 | Corning Incorporated | Optical fibers prepared with a primary coating composition including a monomer with a pendant hydroxyl functional group |
DE10012580A1 (de) * | 2000-03-15 | 2001-09-27 | Basf Coatings Ag | Verfahren zur Herstellung von Beschichtungen, Klebschichten und Dichtungen aus mit aktinischer Strahlung härtbaren Beschichtungsstoffen, Klebstoffen und Dichtungsmassen |
US6535673B1 (en) * | 2000-03-30 | 2003-03-18 | Corning Cable Systems Llc | Optical fiber arrays having an interface characteristic |
ATE322469T1 (de) * | 2000-06-22 | 2006-04-15 | Prysmian Cavi Sistemi Energia | Gefärbte optische faser und diese faser enthaltendes optisches faserband |
US6489376B1 (en) * | 2000-07-31 | 2002-12-03 | Alcatel | Formulation of UV-curable coatings for optical fiber for a fast cure |
WO2002088793A1 (en) * | 2001-04-30 | 2002-11-07 | Schott Glas | Use of sol-gel as an inorganic adhesive for high stability, self-organizing, fiber optic array |
US6678449B2 (en) | 2001-07-10 | 2004-01-13 | Alcatel | Visibly distinguishable colored optical fiber ribbons |
US7068902B2 (en) * | 2001-08-17 | 2006-06-27 | Alcatel | Radiation-curable coating composition for optical fibers comprising all-in-one oligomeric system |
US7105583B2 (en) * | 2001-12-20 | 2006-09-12 | Ppg Industries Ohio, Inc. | Radiation-curable compositions for optical fiber coating materials |
US7403687B2 (en) | 2001-12-21 | 2008-07-22 | Pirelli Communications Cables And Systems Usa, Llc | Reinforced tight-buffered optical fiber and cables made with same |
US6859600B2 (en) * | 2002-05-30 | 2005-02-22 | Alcatel | Coated optical fiber and optical fiber ribbon and method for the fabrication thereof |
JP3982377B2 (ja) * | 2002-10-08 | 2007-09-26 | Jsr株式会社 | 光硬化性樹脂組成物及び光学部材 |
US7211368B2 (en) * | 2003-01-07 | 2007-05-01 | 3 Birds, Inc. | Stereolithography resins and methods |
FR2854956B1 (fr) * | 2003-05-16 | 2005-11-04 | Nexans | Composition liquide photoreticulaire pour fibre plastique |
US7532795B2 (en) * | 2003-08-20 | 2009-05-12 | Dsm Ip Assets B.V. | Radiation-curable liquid resin composition |
JP2005066836A (ja) * | 2003-08-22 | 2005-03-17 | Three M Innovative Properties Co | 可とう性成形型及びその製造方法ならびに微細構造体の製造方法 |
US7361409B2 (en) * | 2003-08-22 | 2008-04-22 | 3M Innovative Properties Company | Microstructured article comprising a polymerized composition having low glass transition temperature |
WO2005035461A1 (en) * | 2003-10-17 | 2005-04-21 | Dsm Ip Assets B.V. | Flame retardant uv cured buffered optical fibers and buffer composition |
GB0329597D0 (en) * | 2003-12-20 | 2004-01-28 | Avecia Ltd | Compositions |
WO2006088930A2 (en) * | 2005-02-17 | 2006-08-24 | 3M Innovative Properties Company | Brightness enhancement film comprising polymerized organic phase having low glass transition temperature |
US20060235107A1 (en) * | 2005-04-15 | 2006-10-19 | 3M Innovative Properties Company | Method of reusing flexible mold and microstructure precursor composition |
US7478791B2 (en) * | 2005-04-15 | 2009-01-20 | 3M Innovative Properties Company | Flexible mold comprising cured polymerizable resin composition |
JP2007070618A (ja) * | 2005-08-09 | 2007-03-22 | Mitsubishi Plastics Ind Ltd | 光硬化性組成物 |
WO2008027658A1 (en) * | 2006-09-01 | 2008-03-06 | 3M Innovative Properties Company | Method of making display component with curable paste composition |
US8920885B2 (en) | 2006-11-21 | 2014-12-30 | Dr. Ben Curatolo, Inc. | Corrosion-resistant, chromium-free, self-priming coatings curable by ultraviolet light |
JP2010509643A (ja) * | 2006-12-14 | 2010-03-25 | ディーエスエム アイピー アセッツ ビー.ブイ. | D1365bj光ファイバのための放射線硬化性一次被覆 |
WO2008076285A1 (en) * | 2006-12-14 | 2008-06-26 | Dsm Ip Assets B.V. | D1364 bt secondary coating on optical fiber |
EP2091880B1 (en) * | 2006-12-14 | 2011-02-23 | DSM IP Assets B.V. | D1379 p radiation curable primary coating on optical fiber |
EP2305617B1 (en) | 2006-12-14 | 2014-01-22 | DSM IP Assets B.V. | D1381 Supercoatings for optical fiber |
KR101104971B1 (ko) * | 2006-12-14 | 2012-01-16 | 디에스엠 아이피 어셋츠 비.브이. | 광섬유용 d1369 d 방사선 경화성 2차 코팅 |
RU2439112C2 (ru) * | 2006-12-14 | 2012-01-10 | ДСМ Ай Пи ЭССЕТС Б.В. | Отверждаемое излучением первичное покрытие d1378 ca для оптического волокна |
WO2008076299A1 (en) * | 2006-12-14 | 2008-06-26 | Dsm Ip Assets B.V. | D1363 bt radiation curable primary coatings on optical fiber |
JP2010509449A (ja) * | 2006-12-14 | 2010-03-25 | ディーエスエム アイピー アセッツ ビー.ブイ. | D1370r光ファイバのための放射線硬化性二次被覆 |
US20080226914A1 (en) * | 2006-12-14 | 2008-09-18 | Norlin Tyson Dean | D1368 cr radiation curable primary coating for optical fiber |
JP5388817B2 (ja) * | 2008-12-12 | 2014-01-15 | キヤノン株式会社 | 液体吐出ヘッドの製造方法 |
WO2011098514A1 (en) | 2010-02-11 | 2011-08-18 | Dsm Ip Assets B.V. | Radiation curable liquid composition for low gloss coatings |
KR101007769B1 (ko) * | 2010-04-23 | 2011-01-14 | 동우 화인켐 주식회사 | 수지형 도광판용 조성물, 이로 형성된 도광판을 포함하는 백라이트 유닛 및 상기 백라이트 유닛을 구비하는 액정표시장치 |
JP5747626B2 (ja) * | 2011-03-30 | 2015-07-15 | 大日本印刷株式会社 | 加飾シート及びこれを用いた加飾樹脂成形品 |
CN102898958B (zh) * | 2011-07-25 | 2016-11-02 | 汉高股份有限公司 | 一种粘合剂组合物 |
US9046670B2 (en) * | 2011-10-19 | 2015-06-02 | Chromis Fiberoptics, Inc. | Monolithic polymer optical fiber ribbon |
AU2013323664B2 (en) * | 2012-09-28 | 2017-12-07 | Adc Telecommunications, Inc. | Manufacture and testing of fiber optic cassette |
US9223094B2 (en) | 2012-10-05 | 2015-12-29 | Tyco Electronics Nederland Bv | Flexible optical circuit, cassettes, and methods |
CN105602168B (zh) * | 2014-10-05 | 2017-10-31 | 绍兴酷易网络科技服务有限公司 | 一种层绞式带状光缆 |
KR101869307B1 (ko) * | 2016-08-31 | 2018-06-21 | 조광페인트주식회사 | Pvc 바닥재용 uv 경화형 무광도료 조성물 및 이를 이용한 코팅방법 |
WO2018116901A1 (ja) * | 2016-12-19 | 2018-06-28 | Dic株式会社 | 重合性組成物、及び、それを用いた光学異方体 |
WO2019070682A2 (en) | 2017-10-02 | 2019-04-11 | Commscope Technologies Llc | OPTICAL CIRCUIT AND PREPARATION METHOD |
EP3891541A4 (en) * | 2018-11-05 | 2022-11-02 | Sterlite Technologies Limited | MATRIX MATERIAL FOR ROLLABLE FIBER OPTIC RIBBONS |
TW202200629A (zh) * | 2020-03-19 | 2022-01-01 | 日商巴川製紙所股份有限公司 | 異方性光學膜用組成物及異方性光學膜 |
Family Cites Families (74)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AT261266B (de) * | 1965-09-18 | 1968-04-10 | Schneider Co Optische Werke | Faseroptischer Analog-Digital-Umsetzer |
US3912516A (en) * | 1973-07-27 | 1975-10-14 | Upjohn Co | Photopolyer composition containing a polyurethane binding agent |
US4123137A (en) * | 1975-04-24 | 1978-10-31 | Bell Telephone Laboratories, Incorporated | Optical fiber arrangement for splicing fibers secured to ribbonlike tape |
US4065587A (en) * | 1976-05-11 | 1977-12-27 | Scm Corporation | U.V. Curable poly(ether-urethane) polyacrylates and wet-look polymers prepared therefrom |
US4116786A (en) * | 1976-06-08 | 1978-09-26 | Union Carbide Corporation | Radiation curable coating compositions containing an acrylate-capped, polyether urethane and a polysiloxane |
CH628622A5 (de) * | 1976-12-24 | 1982-03-15 | Ciba Geigy Ag | Verfahren zur herstellung von neuen in 4-stellung substituierten 3-sulfamoylbenzoesaeuren. |
US4139436A (en) * | 1977-02-07 | 1979-02-13 | The Goodyear Tire & Rubber Company | Polyetherurethane composition and polymer prepared by photopolymerization |
US4131602A (en) * | 1977-09-29 | 1978-12-26 | Union Carbide Corporation | Radiation curable acrylated polyurethane |
US4130708A (en) * | 1977-12-09 | 1978-12-19 | Ppg Industries, Inc. | Siloxane urethane acrylate radiation curable compounds for use in coating compositions |
US4188455A (en) * | 1978-01-03 | 1980-02-12 | Lord Corporation | Actinic radiation-curable formulations containing at least one unsaturated polyether-esterurethane oligomer |
US4133723A (en) * | 1978-01-03 | 1979-01-09 | Lord Corporation | Actinic radiation-curable formulations from the reaction product of organic isocyanate, poly(alkylene oxide) polyol and an unsaturated addition-polymerizable monomeric compound having a single isocyanate-reactive hydrogen group |
US4246379A (en) * | 1978-05-01 | 1981-01-20 | Lord Corporation | Radiation curable coating compositions |
US4326010A (en) * | 1979-06-15 | 1982-04-20 | E. I. Du Pont De Nemours And Company | Additive in a photopolymerizable composition for reducing its adhesion to a support film |
US4369300A (en) * | 1979-11-26 | 1983-01-18 | Union Carbide Corporation | Acrylated urethane silicone compositions |
US4324575A (en) * | 1980-08-11 | 1982-04-13 | Bell Telephone Laboratories, Incorporated | Low TG soft UV-curable coatings |
US4438190A (en) * | 1981-03-04 | 1984-03-20 | Hitachi Chemical Company, Ltd. | Photosensitive resin composition containing unsaturated monomers and unsaturated phosphates |
US4567107A (en) * | 1982-05-05 | 1986-01-28 | Essex Specialty Products, Inc. | Acrylic resin having pendant silane groups thereon, and methods of making and using the same |
US4496210A (en) * | 1982-07-19 | 1985-01-29 | Desoto, Inc. | Low temperature-flexible radiation-curable unsaturated polysiloxane coated fiber optic |
US4477548A (en) * | 1982-09-02 | 1984-10-16 | Eastman Kodak Company | Radiation-curable overcoat compositions and toner-imaged elements containing same |
US4435461A (en) * | 1982-10-19 | 1984-03-06 | Scott Paper Company | Method of providing a surface effect in a release paper product |
NZ205990A (en) * | 1982-11-05 | 1987-04-30 | Deltaglass Sa | Radiation-curable, urethane acrylate-containing liquid adhesive composition and glass laminates |
US4932750A (en) * | 1982-12-09 | 1990-06-12 | Desoto, Inc. | Single-coated optical fiber |
US4472021A (en) * | 1982-12-10 | 1984-09-18 | Desoto, Inc. | Strippable radiation-cured coatings for optical fiber and method |
US4462286A (en) * | 1982-12-23 | 1984-07-31 | The United States Of America As Represented By The Secretary Of The Air Force | Portable slotting device |
US4472019A (en) * | 1982-12-28 | 1984-09-18 | Desoto, Inc. | Topcoats for buffer-coated optical fiber using urethane acrylate and epoxy acrylate and vinyl monomer |
US4512340A (en) * | 1983-02-22 | 1985-04-23 | Johnson & Johnson Products, Inc. | Visible light cured orthopedic polymer casts |
US4533445A (en) * | 1983-07-06 | 1985-08-06 | Shipley Company Inc. | U.V. Curable composition |
NL8303251A (nl) * | 1983-09-22 | 1985-04-16 | Philips Nv | Werkwijze voor het optisch verbinden van een lichtgeleider aan een elektrooptische inrichting. |
US4588787A (en) * | 1983-10-13 | 1986-05-13 | Ford Motor Company | Flexible two component urethane coating compositions |
US4849462A (en) * | 1983-11-10 | 1989-07-18 | Desoto, Inc. | Ultraviolet-curable coatings for optical glass fibers having improved adhesion |
JPS60191039A (ja) * | 1984-03-07 | 1985-09-28 | Shin Etsu Chem Co Ltd | 光フアイバ−用被覆材 |
US4561950A (en) * | 1984-04-02 | 1985-12-31 | Desoto, Inc. | Post-formable radiation-curing coatings |
GB8408621D0 (en) * | 1984-04-04 | 1984-05-16 | Dow Corning Ltd | Curable organopolysiloxane compositions |
US4496686A (en) * | 1984-05-07 | 1985-01-29 | Desoto, Inc. | Radiation-curable coatings containing reactive pigment dispersants |
NL8401982A (nl) * | 1984-06-22 | 1986-01-16 | Philips Nv | Optische glasvezel voorzien van een kunststofbedekking. |
US4762751A (en) * | 1984-07-30 | 1988-08-09 | Ppg Industries, Inc. | Flexible, chemically treated bundles of fibers, woven and nonwoven fabrics and coated bundles and fabrics thereof |
US4600649A (en) * | 1984-10-22 | 1986-07-15 | Desoto, Inc. | Abrasion-resistant ultraviolet-curable coatings |
US4744631A (en) * | 1985-01-31 | 1988-05-17 | American Telephone And Telegraph Company, At&T Bell Laboratories | Single mode optical fiber ribbon cable |
US4701016A (en) * | 1985-01-31 | 1987-10-20 | American Telephone And Telegraph Company, At&T Bell Laboratories | Thixotropic grease composition and cable comprising same |
JPS61179216A (ja) * | 1985-02-04 | 1986-08-11 | Sanyo Kokusaku Pulp Co Ltd | 光硬化性樹脂組成物 |
US4629287A (en) * | 1985-02-25 | 1986-12-16 | Desoto, Inc. | Ultraviolet curable buffer coatings for optical fiber |
GB8506499D0 (en) * | 1985-03-13 | 1985-04-17 | Telephone Cables Ltd | Optical fibre assemblies/cables |
US4707076A (en) * | 1985-04-12 | 1987-11-17 | Ensign-Bickford Industries, Inc. | Coating compositions for optical fibers |
US4608409A (en) * | 1985-05-08 | 1986-08-26 | Desoto, Inc. | Polyacrylated oligomers in ultraviolet curable optical fiber coatings |
US4806574A (en) * | 1985-07-22 | 1989-02-21 | Desoto, Inc. | Ultraviolet curable coatings for optical glass fiber based on a polyfunctional core |
US4786586A (en) * | 1985-08-06 | 1988-11-22 | Morton Thiokol, Inc. | Radiation curable coating for photographic laminate |
NL8502402A (nl) * | 1985-09-03 | 1987-04-01 | Philips Nv | Optische vezel voorzien van een kunststofbedekking, en werkwijze en inrichting voor de vervaardiging van een dergelijke optische vezel. |
JPS62119141A (ja) * | 1985-11-19 | 1987-05-30 | Shin Etsu Chem Co Ltd | 放射線硬化性光フアイバ−用被覆剤 |
JPS62123044A (ja) * | 1985-11-22 | 1987-06-04 | Nippon Soda Co Ltd | 光学ガラスフアイバ用被覆材 |
JPH0751454B2 (ja) * | 1986-03-10 | 1995-06-05 | 古河電気工業株式会社 | 光フアイバ用紫外線硬化性被覆材料 |
EP0241027A3 (en) * | 1986-04-11 | 1989-12-13 | Takeda Chemical Industries, Ltd. | An adhesive composition |
JPS62249992A (ja) * | 1986-04-24 | 1987-10-30 | Nippon Kayaku Co Ltd | 新規なシリコンウレタン(メタ)アクリレ−ト,これを用いた樹脂組成物およびコ−テイング剤 |
JPS6335438A (ja) * | 1986-07-30 | 1988-02-16 | Nitto Electric Ind Co Ltd | 光学ガラスフアイバ用被覆材料 |
JPS6390526A (ja) * | 1986-10-03 | 1988-04-21 | Sumitomo Chem Co Ltd | 硬化性樹脂組成物 |
JP2525177B2 (ja) * | 1987-04-30 | 1996-08-14 | ディーエスエム・エヌヴィ | 光フアイバ−被覆用組成物 |
JPS63281109A (ja) * | 1987-05-13 | 1988-11-17 | Sumitomo Electric Ind Ltd | 光伝送用フアイバ |
JPS6424816A (en) * | 1987-07-21 | 1989-01-26 | Mitsui Toatsu Chemicals | Photo-setting resin composition |
US4843462A (en) * | 1987-09-04 | 1989-06-27 | Adt Security Systems, Inc. | Remote video observation systems |
JPH0730141B2 (ja) * | 1987-09-24 | 1995-04-05 | 信越化学工業株式会社 | 紫外線硬化性液状組成物 |
US4844064A (en) | 1987-09-30 | 1989-07-04 | Baxter Travenol Laboratories, Inc. | Surgical cutting instrument with end and side openings |
JPH07113104B2 (ja) * | 1987-11-13 | 1995-12-06 | 日本合成ゴム株式会社 | 光フアイバー用硬化性バンドリング材 |
US4900126A (en) * | 1988-06-30 | 1990-02-13 | American Telephone & Telegraph Co. | Bonded array of transmission media |
JP2610491B2 (ja) * | 1988-09-09 | 1997-05-14 | デー エス エム エヌ.ヴェー. | 液状硬化性樹脂組成物 |
JP2601699B2 (ja) * | 1988-09-28 | 1997-04-16 | デー エス エム エヌ.ヴェー. | 液状硬化性樹脂組成物 |
JPH02135211A (ja) * | 1988-11-15 | 1990-05-24 | Yokohama Rubber Co Ltd:The | 紫外線硬化型樹脂組成物 |
CA1341128C (en) | 1989-06-27 | 2000-10-24 | Borden Chemical, Inc. | Optical fiber array |
JP3043188B2 (ja) * | 1992-10-15 | 2000-05-22 | シャープ株式会社 | 文書処理装置 |
JP4209943B2 (ja) * | 1995-08-01 | 2009-01-14 | コニンクリーケ デーエスエム ナムローゼ フェンノートシャップ | リボンユニット、リボンユニットを製造する方法、およびミッドスパンアクセスを与える方法 |
US6052503A (en) | 1995-09-07 | 2000-04-18 | Dsm N.V. | Optical glass fiber ribbon assembly and radiation curable matrix forming composition |
US5908873A (en) * | 1995-12-20 | 1999-06-01 | Borden Chemicals, Inc. | Peelable bonded ribbon matrix material; optical fiber bonded ribbon arrays containing same; and process for preparing said optical fiber bonded ribbon arrays |
JP3746871B2 (ja) * | 1997-04-14 | 2006-02-15 | Jsr株式会社 | 液状硬化性樹脂組成物 |
US6197422B1 (en) * | 1997-05-06 | 2001-03-06 | Dsm, N.V. | Ribbon assemblies and radiation-curable ink compositions for use in forming the ribbon assemblies |
US6085010A (en) * | 1997-06-11 | 2000-07-04 | Dsm N.V. | Optical glass fiber ribbon assemblies and radiation-curable compositions for use in forming ribbon assemblies |
US6134364A (en) * | 1998-09-18 | 2000-10-17 | Lucent Technologies Inc. | Optical fiber ribbon |
-
1989
- 1989-09-22 CA CA000612561A patent/CA1341128C/en not_active Expired - Fee Related
-
1990
- 1990-01-17 AU AU48532/90A patent/AU622752B2/en not_active Ceased
- 1990-04-20 DK DK90304243.0T patent/DK0407004T3/da active
- 1990-04-20 AT AT90304243T patent/ATE141301T1/de not_active IP Right Cessation
- 1990-04-20 EP EP90304243A patent/EP0407004B1/en not_active Revoked
- 1990-04-20 DE DE69028051T patent/DE69028051T2/de not_active Expired - Fee Related
- 1990-04-20 ES ES90304243T patent/ES2090096T3/es not_active Expired - Lifetime
- 1990-06-26 JP JP2168170A patent/JPH0339314A/ja active Pending
- 1990-06-26 KR KR1019900009481A patent/KR100204260B1/ko not_active Expired - Lifetime
-
1994
- 1994-03-17 US US08/187,006 patent/US5881194A/en not_active Expired - Lifetime
-
1996
- 1996-08-16 GR GR960402147T patent/GR3020823T3/el unknown
-
1999
- 1999-03-01 US US09/259,343 patent/US6122428A/en not_active Expired - Lifetime
-
2000
- 2000-06-06 US US09/588,019 patent/US6449413B1/en not_active Expired - Lifetime
- 2000-12-08 JP JP2000374602A patent/JP3444855B2/ja not_active Expired - Lifetime
-
2002
- 2002-12-24 JP JP2002372686A patent/JP3441725B2/ja not_active Expired - Lifetime
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100571475B1 (ko) * | 2002-05-13 | 2006-04-17 | 주식회사 루밴틱스 | 광섬유 리본 코팅용 난연성 수지 조성물 |
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DK0407004T3 (da) | 1996-12-09 |
JP3441725B2 (ja) | 2003-09-02 |
JP2001215373A (ja) | 2001-08-10 |
KR910001408A (ko) | 1991-01-30 |
GR3020823T3 (en) | 1996-11-30 |
DE69028051D1 (de) | 1996-09-19 |
ES2090096T3 (es) | 1996-10-16 |
EP0407004A3 (en) | 1991-12-04 |
US6122428A (en) | 2000-09-19 |
EP0407004B1 (en) | 1996-08-14 |
CA1341128C (en) | 2000-10-24 |
US6449413B1 (en) | 2002-09-10 |
ATE141301T1 (de) | 1996-08-15 |
AU4853290A (en) | 1991-01-10 |
US5881194A (en) | 1999-03-09 |
EP0407004A2 (en) | 1991-01-09 |
AU622752B2 (en) | 1992-04-16 |
JP2003185895A (ja) | 2003-07-03 |
JP3444855B2 (ja) | 2003-09-08 |
JPH0339314A (ja) | 1991-02-20 |
DE69028051T2 (de) | 1997-01-02 |
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