CN1434788A - 光学纤维涂层组合物 - Google Patents
光学纤维涂层组合物 Download PDFInfo
- Publication number
- CN1434788A CN1434788A CN00819107A CN00819107A CN1434788A CN 1434788 A CN1434788 A CN 1434788A CN 00819107 A CN00819107 A CN 00819107A CN 00819107 A CN00819107 A CN 00819107A CN 1434788 A CN1434788 A CN 1434788A
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- Prior art keywords
- composition
- oligopolymer
- coating
- radiation
- optical fiber
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- 239000013307 optical fiber Substances 0.000 title claims description 51
- 239000008199 coating composition Substances 0.000 title claims description 18
- 239000000203 mixture Substances 0.000 claims abstract description 61
- 239000000463 material Substances 0.000 claims abstract description 50
- 239000000654 additive Substances 0.000 claims abstract description 42
- 239000000835 fiber Substances 0.000 claims abstract description 34
- 230000000996 additive effect Effects 0.000 claims abstract description 27
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 claims abstract description 25
- 239000000178 monomer Substances 0.000 claims abstract description 23
- 125000000524 functional group Chemical group 0.000 claims abstract description 19
- 230000005855 radiation Effects 0.000 claims abstract description 9
- -1 aminosiloxane Chemical class 0.000 claims description 74
- 238000000576 coating method Methods 0.000 claims description 73
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- 239000000049 pigment Substances 0.000 claims description 37
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- 229920001296 polysiloxane Polymers 0.000 claims description 23
- 239000000758 substrate Substances 0.000 claims description 17
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- 239000004205 dimethyl polysiloxane Substances 0.000 claims description 10
- 125000001931 aliphatic group Chemical group 0.000 claims description 7
- 239000000975 dye Substances 0.000 claims description 6
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims description 5
- 238000003847 radiation curing Methods 0.000 claims 3
- 239000007795 chemical reaction product Substances 0.000 claims 2
- 239000011159 matrix material Substances 0.000 abstract description 5
- 125000001302 tertiary amino group Chemical group 0.000 abstract description 4
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- 238000002955 isolation Methods 0.000 description 10
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 9
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- NRCMAYZCPIVABH-UHFFFAOYSA-N Quinacridone Chemical compound N1C2=CC=CC=C2C(=O)C2=C1C=C1C(=O)C3=CC=CC=C3NC1=C2 NRCMAYZCPIVABH-UHFFFAOYSA-N 0.000 description 3
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- 238000007348 radical reaction Methods 0.000 description 3
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- 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 description 2
- MTZUIIAIAKMWLI-UHFFFAOYSA-N 1,2-diisocyanatobenzene Chemical compound O=C=NC1=CC=CC=C1N=C=O MTZUIIAIAKMWLI-UHFFFAOYSA-N 0.000 description 2
- ZXHZWRZAWJVPIC-UHFFFAOYSA-N 1,2-diisocyanatonaphthalene Chemical compound C1=CC=CC2=C(N=C=O)C(N=C=O)=CC=C21 ZXHZWRZAWJVPIC-UHFFFAOYSA-N 0.000 description 2
- RTTZISZSHSCFRH-UHFFFAOYSA-N 1,3-bis(isocyanatomethyl)benzene Chemical compound O=C=NCC1=CC=CC(CN=C=O)=C1 RTTZISZSHSCFRH-UHFFFAOYSA-N 0.000 description 2
- ZNPSUOAGONLMLK-UHFFFAOYSA-N 1-ethylpiperidin-3-ol Chemical compound CCN1CCCC(O)C1 ZNPSUOAGONLMLK-UHFFFAOYSA-N 0.000 description 2
- MNAHQWDCXOHBHK-UHFFFAOYSA-N 1-phenylpropane-1,1-diol Chemical compound CCC(O)(O)C1=CC=CC=C1 MNAHQWDCXOHBHK-UHFFFAOYSA-N 0.000 description 2
- KKFDCBRMNNSAAW-UHFFFAOYSA-N 2-(morpholin-4-yl)ethanol Chemical compound OCCN1CCOCC1 KKFDCBRMNNSAAW-UHFFFAOYSA-N 0.000 description 2
- INQDDHNZXOAFFD-UHFFFAOYSA-N 2-[2-(2-prop-2-enoyloxyethoxy)ethoxy]ethyl prop-2-enoate Chemical compound C=CC(=O)OCCOCCOCCOC(=O)C=C INQDDHNZXOAFFD-UHFFFAOYSA-N 0.000 description 2
- SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 description 2
- PYSGFFTXMUWEOT-UHFFFAOYSA-N 3-(dimethylamino)propan-1-ol Chemical compound CN(C)CCCO PYSGFFTXMUWEOT-UHFFFAOYSA-N 0.000 description 2
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 2
- KGWDUNBJIMUFAP-KVVVOXFISA-N Ethanolamine Oleate Chemical compound NCCO.CCCCCCCC\C=C/CCCCCCCC(O)=O KGWDUNBJIMUFAP-KVVVOXFISA-N 0.000 description 2
- OWIKHYCFFJSOEH-UHFFFAOYSA-N Isocyanic acid Chemical compound N=C=O OWIKHYCFFJSOEH-UHFFFAOYSA-N 0.000 description 2
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- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 239000005864 Sulphur Substances 0.000 description 2
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
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- 239000002253 acid Substances 0.000 description 2
- 125000002723 alicyclic group Chemical group 0.000 description 2
- 125000003277 amino group Chemical group 0.000 description 2
- XLJMAIOERFSOGZ-UHFFFAOYSA-N anhydrous cyanic acid Natural products OC#N XLJMAIOERFSOGZ-UHFFFAOYSA-N 0.000 description 2
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 2
- 150000004056 anthraquinones Chemical class 0.000 description 2
- 238000000429 assembly Methods 0.000 description 2
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- UJMDYLWCYJJYMO-UHFFFAOYSA-N benzene-1,2,3-tricarboxylic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1C(O)=O UJMDYLWCYJJYMO-UHFFFAOYSA-N 0.000 description 2
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 2
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- 125000004106 butoxy group Chemical group [*]OC([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
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- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 2
- 150000005690 diesters Chemical class 0.000 description 2
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- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 1
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- ZCQWOFVYLHDMMC-UHFFFAOYSA-N Oxazole Chemical compound C1=COC=N1 ZCQWOFVYLHDMMC-UHFFFAOYSA-N 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 description 1
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 1
- AWMVMTVKBNGEAK-UHFFFAOYSA-N Styrene oxide Chemical compound C1OC1C1=CC=CC=C1 AWMVMTVKBNGEAK-UHFFFAOYSA-N 0.000 description 1
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 description 1
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Natural products CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 1
- 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 description 1
- KNSXNCFKSZZHEA-UHFFFAOYSA-N [3-prop-2-enoyloxy-2,2-bis(prop-2-enoyloxymethyl)propyl] prop-2-enoate Chemical compound C=CC(=O)OCC(COC(=O)C=C)(COC(=O)C=C)COC(=O)C=C KNSXNCFKSZZHEA-UHFFFAOYSA-N 0.000 description 1
- FHLPGTXWCFQMIU-UHFFFAOYSA-N [4-[2-(4-prop-2-enoyloxyphenyl)propan-2-yl]phenyl] prop-2-enoate Chemical class 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 description 1
- 238000007259 addition reaction Methods 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- 125000000746 allylic group Chemical group 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- QUDWYFHPNIMBFC-UHFFFAOYSA-N bis(prop-2-enyl) benzene-1,2-dicarboxylate Chemical compound C=CCOC(=O)C1=CC=CC=C1C(=O)OCC=C QUDWYFHPNIMBFC-UHFFFAOYSA-N 0.000 description 1
- MQDJYUACMFCOFT-UHFFFAOYSA-N bis[2-(1-hydroxycyclohexyl)phenyl]methanone Chemical compound C=1C=CC=C(C(=O)C=2C(=CC=CC=2)C2(O)CCCCC2)C=1C1(O)CCCCC1 MQDJYUACMFCOFT-UHFFFAOYSA-N 0.000 description 1
- OHJMTUPIZMNBFR-UHFFFAOYSA-N biuret Chemical class NC(=O)NC(N)=O OHJMTUPIZMNBFR-UHFFFAOYSA-N 0.000 description 1
- 239000000038 blue colorant Substances 0.000 description 1
- 239000001055 blue pigment Substances 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- RFAFBXGYHBOUMV-UHFFFAOYSA-N calcium chromate Chemical compound [Ca+2].[O-][Cr]([O-])(=O)=O RFAFBXGYHBOUMV-UHFFFAOYSA-N 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- FWLDHHJLVGRRHD-UHFFFAOYSA-N decyl prop-2-enoate Chemical compound CCCCCCCCCCOC(=O)C=C FWLDHHJLVGRRHD-UHFFFAOYSA-N 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 125000005442 diisocyanate group Chemical group 0.000 description 1
- 239000000539 dimer Substances 0.000 description 1
- ZZVUWRFHKOJYTH-UHFFFAOYSA-N diphenhydramine Chemical compound C=1C=CC=CC=1C(OCCN(C)C)C1=CC=CC=C1 ZZVUWRFHKOJYTH-UHFFFAOYSA-N 0.000 description 1
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- UYMKPFRHYYNDTL-UHFFFAOYSA-N ethenamine Chemical compound NC=C UYMKPFRHYYNDTL-UHFFFAOYSA-N 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- UHESRSKEBRADOO-UHFFFAOYSA-N ethyl carbamate;prop-2-enoic acid Chemical compound OC(=O)C=C.CCOC(N)=O UHESRSKEBRADOO-UHFFFAOYSA-N 0.000 description 1
- WGOQVOGFDLVJAW-UHFFFAOYSA-N ethyl carbamate;prop-2-enoic acid Chemical compound OC(=O)C=C.OC(=O)C=C.OC(=O)C=C.CCOC(N)=O WGOQVOGFDLVJAW-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 210000003811 finger Anatomy 0.000 description 1
- 238000005189 flocculation Methods 0.000 description 1
- 230000016615 flocculation Effects 0.000 description 1
- 210000005224 forefinger Anatomy 0.000 description 1
- 238000007306 functionalization reaction Methods 0.000 description 1
- 150000002240 furans Chemical class 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 238000009998 heat setting Methods 0.000 description 1
- 229940051250 hexylene glycol Drugs 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- PBOSTUDLECTMNL-UHFFFAOYSA-N lauryl acrylate Chemical compound CCCCCCCCCCCCOC(=O)C=C PBOSTUDLECTMNL-UHFFFAOYSA-N 0.000 description 1
- 150000002632 lipids Chemical class 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- ZQXSMRAEXCEDJD-UHFFFAOYSA-N n-ethenylformamide Chemical compound C=CNC=O ZQXSMRAEXCEDJD-UHFFFAOYSA-N 0.000 description 1
- 150000004780 naphthols Chemical class 0.000 description 1
- HKKDKUMUWRTAIA-UHFFFAOYSA-N nitridooxidocarbon(.) Chemical compound [O]C#N HKKDKUMUWRTAIA-UHFFFAOYSA-N 0.000 description 1
- 125000000018 nitroso group Chemical group N(=O)* 0.000 description 1
- UQIQLMWVCFRJKB-UHFFFAOYSA-N nonoxybenzene;prop-2-enoic acid Chemical compound OC(=O)C=C.CCCCCCCCCOC1=CC=CC=C1 UQIQLMWVCFRJKB-UHFFFAOYSA-N 0.000 description 1
- 125000005574 norbornylene group Chemical group 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 238000005457 optimization Methods 0.000 description 1
- 239000001053 orange pigment Substances 0.000 description 1
- RPQRDASANLAFCM-UHFFFAOYSA-N oxiran-2-ylmethyl prop-2-enoate Chemical compound C=CC(=O)OCC1CO1 RPQRDASANLAFCM-UHFFFAOYSA-N 0.000 description 1
- 125000005702 oxyalkylene group Chemical group 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920006267 polyester film Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 230000001737 promoting effect Effects 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
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 239000001054 red pigment Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000007790 scraping Methods 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 229930192474 thiophene Natural products 0.000 description 1
- 210000003813 thumb Anatomy 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 125000005425 toluyl group Chemical group 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000012463 white pigment Substances 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
- 239000001060 yellow colorant Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C25/00—Surface treatment of fibres or filaments made from glass, minerals or slags
- C03C25/10—Coating
- C03C25/104—Coating to obtain optical fibres
- C03C25/106—Single coatings
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Geochemistry & Mineralogy (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Paints Or Removers (AREA)
- Optical Fibers, Optical Fiber Cores, And Optical Fiber Bundles (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Surface Treatment Of Glass Fibres Or Filaments (AREA)
- Macromonomer-Based Addition Polymer (AREA)
Abstract
Description
实施例1 | 实施例2 | 实施例3 | 实施例4 | 实施例5 | |
透明油墨基底 | 白色 | 红色 | 黄色 | 蓝色 | |
低聚物A | 30.45 | 26.00 | 23.52 | 24.35 | 26.58 |
PETTA | 15.26 | 13.03 | 11.79 | 12.20 | 13.32 |
TMPTA | 9.10 | 7.77 | 7.03 | 7.28 | 7.94 |
HDDA | 7.13 | 6.09 | 5.51 | 5.70 | 6.22 |
IBOA | 7.03 | 6.00 | 5.43 | 5.62 | 6.14 |
低聚物B | 20.00 | 17.07 | 15.45 | 16.00 | 17.46 |
BHT | 0.57 | 0.49 | 0.44 | 0.46 | 0.50 |
添加剂A | 3.88 | 3.31 | 3.00 | 3.10 | 3.39 |
光敏引发剂A | 2.00 | 1.71 | 1.55 | 1.60 | 1.75 |
光敏引发剂C | 4.58 | 3.91 | 3.54 | 3.66 | 4.00 |
白着色剂 | 0.0 | 14.38 | 2.38 | 10.56 | 1.00 |
黄着色剂 | 0.0 | 0.00 | 0.00 | 9.21 | 0.00 |
红着色剂 | 0.0 | 0.00 | 16.01 | 0.00 | 0.00 |
蓝着色剂 | 0.0 | 0.00 | 0.00 | 0.00 | 11.45 |
稳定剂A | 0.25 | 0.25 | 0.25 | 0.25 | 0.25 |
总计 | 100.00 | 100.00 | 100.00 | 100.00 | 100.00 |
组分 | 实施例6 | 实施例7 |
低聚物A | 31.35 | 32.31 |
HDDA | 21.83 | 22.48 |
低聚物C | 20.90 | 21.54 |
添加剂B | 2.20 | 2.27 |
BHT | 0.48 | 0.50 |
光敏引发剂A | 1.37 | 1.41 |
光敏引发剂B | 2.75 | 2.83 |
光敏引发剂C | 3.85 | 3.96 |
着色剂:白 | 15.02 | 1.00 |
着色剂:蓝 | 0.0 | 11.45 |
稳定剂A | 0.25 | 0.25 |
总计 | 100.00 | 100.00 |
中跨接入性 | 通过 | 通过 |
组分 | 实施例F | 实施例G | 实施例H | 实施例J | 实施例K | 实施例L | 实施例M | 实施例N | 实施例P | 实施例Q | 实施例R |
二甲基乙醇胺 | 5.72 | 11.61 | 10.89 | 11.45 | |||||||
二乙醇胺 | 12.14 | ||||||||||
1-乙基-3-羟基哌啶 | 16.27 | 8.28 | |||||||||
羟乙基吗啉 | 8.24 | 16.33 | |||||||||
二甲基丙醇胺 | 8.64 | 16.91 | |||||||||
IPDI | 14.24 | 28.5 | |||||||||
TMDI | 26.05 | 13.26 | 26.03 | 13.2 | 25.85 | 13.25 | 27.46 | ||||
DESW | 31.99 | ||||||||||
添加剂D | 78.5 | 80.04 | 78.16 | 18.47 | |||||||
添加剂C | 57.68 | 57.64 | 57.24 | 60.93 | 57.12 | 60.05 | |||||
添加剂E | 87.86 | ||||||||||
总计 | 100 | 100 | 100 | 100 | 100 | 100 | 100 | 100 | 100 | 100 | 100 |
组分 | 实施例8 | 实施例9 | 实施例10 | 实施例11 | 实施例12 | 实施例13 | 实验a | 实验b | 实验c | 实验d |
低聚物A | 30.32 | 31.24 | 30.32 | 31.24 | 30.32 | 31.24 | 30.32 | 31.24 | 30.32 | 31.24 |
HDDA | 18.29 | 18.84 | 18.29 | 18.84 | 18.29 | 18.84 | 18.29 | 18.84 | 18.29 | 18.84 |
低聚物C | 15.82 | 16.30 | 15.82 | 16.30 | 15.82 | 16.30 | 15.82 | 16.30 | 15.82 | 16.30 |
添加剂F | 4.41 | 4.54 | ||||||||
添加剂P | 4.41 | 4.54 | ||||||||
添加剂R | 4.41 | 4.54 | ||||||||
Cocamide DEA | 4.41 | 4.54 | ||||||||
CocamidopropylDMA | 4.41 | 4.54 | ||||||||
BHT | 0.48 | 0.50 | 0.48 | 0.50 | 0.48 | 0.50 | 0.48 | 0.50 | 0.48 | 0.50 |
光敏引发剂A | 0.96 | 0.99 | 0.96 | 0.99 | 0.96 | 0.99 | 0.96 | 0.99 | 0.96 | 0.99 |
光敏引发剂B | 3.86 | 3.97 | 3.86 | 3.97 | 3.86 | 3.97 | 3.86 | 3.97 | 3.86 | 3.97 |
光敏引发剂C | 2.89 | 2.98 | 2.89 | 2.98 | 2.89 | 2.98 | 2.89 | 2.98 | 2.89 | 2.98 |
光敏引发剂D | 7.70 | 7.94 | 7.70 | 7.94 | 7.70 | 7.94 | 7.70 | 7.94 | 7.70 | 7.94 |
着色剂:白色 | 15.02 | 1.00 | 15.02 | 1.00 | 15.02 | 1.00 | 15.02 | 1.00 | 15.02 | 1.00 |
着色剂:蓝色 | 11.45 | 11.45 | 11.45 | 11.45 | 11.45 | |||||
稳定剂A | 0.25 | 0.25 | 0.25 | 0.25 | 0.25 | 0.25 | 0.25 | 0.25 | 0.25 | 0.25 |
总计 | 100.00 | 100.00 | 100.00 | 100.00 | 100.00 | 100.00 | 100.00 | 100.00 | 100.00 | 100.00 |
中跨接入性 | 通过 | 通过 | 通过 | 通过 | 通过 | 通过 | 失败 | 失败 | 失败 | 失败 |
Claims (11)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US09/471,694 US6538045B1 (en) | 1999-12-23 | 1999-12-23 | Optical fiber coating compositions containing secondary or tertiary amino silicone-containing additive |
US09/471,694 | 1999-12-23 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN1434788A true CN1434788A (zh) | 2003-08-06 |
CN100347116C CN100347116C (zh) | 2007-11-07 |
Family
ID=23872653
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CNB008191077A Expired - Fee Related CN100347116C (zh) | 1999-12-23 | 2000-12-18 | 光学纤维涂层组合物 |
Country Status (8)
Country | Link |
---|---|
US (2) | US6538045B1 (zh) |
EP (1) | EP1240117A2 (zh) |
JP (1) | JP2003519249A (zh) |
KR (1) | KR100729045B1 (zh) |
CN (1) | CN100347116C (zh) |
AU (1) | AU3243401A (zh) |
BR (1) | BR0017045A (zh) |
WO (1) | WO2001047823A2 (zh) |
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US6827985B2 (en) * | 2001-05-02 | 2004-12-07 | Henkel Corporation | Curable silicone compositions having enhanced cure-through-volume |
KR100471083B1 (ko) | 2002-12-24 | 2005-03-10 | 삼성전자주식회사 | 광섬유 절단장치 |
JP4822892B2 (ja) * | 2005-09-09 | 2011-11-24 | 信越化学工業株式会社 | コーティング剤 |
US7819968B2 (en) * | 2007-03-14 | 2010-10-26 | Sun Chemical Corporation | Stir-in pigment preparations for coloration of energy curable systems |
EP2240331A4 (en) * | 2008-02-01 | 2014-07-30 | Sun Chemical Corp | ENERGY-CURABLE COATING AND INKS WITH IMPROVED RESISTANCE |
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US8877844B2 (en) * | 2013-01-16 | 2014-11-04 | Wacker Chemical Corporation | Highly pigmented aqueous coating compositions with improved resistance to blocking |
US20150090689A1 (en) * | 2013-09-27 | 2015-04-02 | Corning Incorporated | Compositions for protecting display glass and methods of use thereof |
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CN105440782B (zh) * | 2015-12-01 | 2018-06-26 | 武汉长盈通光电技术有限公司 | 一种着色前无需搅拌的光纤着色油墨 |
US10031303B1 (en) | 2017-08-29 | 2018-07-24 | Superior Essex International LP | Methods for forming tight buffered optical fibers using compression to facilitate subsequent loosening |
CN110358353A (zh) * | 2019-07-01 | 2019-10-22 | 浙江瑞通光电材料有限公司 | 一种紫外光固化光纤着色墨组合物及其应用 |
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-
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- 1999-12-23 US US09/471,694 patent/US6538045B1/en not_active Expired - Fee Related
-
2000
- 2000-12-18 JP JP2001549302A patent/JP2003519249A/ja active Pending
- 2000-12-18 BR BR0017045-3A patent/BR0017045A/pt not_active Application Discontinuation
- 2000-12-18 EP EP00991331A patent/EP1240117A2/en not_active Withdrawn
- 2000-12-18 KR KR1020027008146A patent/KR100729045B1/ko not_active IP Right Cessation
- 2000-12-18 WO PCT/NL2000/000928 patent/WO2001047823A2/en not_active Application Discontinuation
- 2000-12-18 AU AU32434/01A patent/AU3243401A/en not_active Abandoned
- 2000-12-18 CN CNB008191077A patent/CN100347116C/zh not_active Expired - Fee Related
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2002
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN107964277A (zh) * | 2017-12-18 | 2018-04-27 | 昆山裕凌电子科技有限公司 | 一种高附着力耐刮擦有机硅刮涂油墨及其制备方法 |
Also Published As
Publication number | Publication date |
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JP2003519249A (ja) | 2003-06-17 |
US7041712B2 (en) | 2006-05-09 |
KR100729045B1 (ko) | 2007-06-14 |
EP1240117A2 (en) | 2002-09-18 |
BR0017045A (pt) | 2002-11-05 |
CN100347116C (zh) | 2007-11-07 |
US20030176523A1 (en) | 2003-09-18 |
KR20020067046A (ko) | 2002-08-21 |
WO2001047823A2 (en) | 2001-07-05 |
WO2001047823A3 (en) | 2001-12-06 |
US6538045B1 (en) | 2003-03-25 |
AU3243401A (en) | 2001-07-09 |
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