LT3310B - Liquid, radiation-cured coating composition for glass surfaces, process for coating, optical glass fibre - Google Patents

Liquid, radiation-cured coating composition for glass surfaces, process for coating, optical glass fibre Download PDF

Info

Publication number: LT3310B
Authority: LT; Lithuania
Prior art keywords: composition; weight; coating; aminopropyltrimethoxysilane; total weight
Prior art date: 1988-12-02

Application number

LTIP529A

Other languages

English (en)

Lithuanian (lt)

Inventor

Stephan Schunck

Original Assignee

Basf Lacke & Farben

Priority date (The priority date 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 date listed.)

1988-12-02

Filing date

1993-05-06

Publication date

1995-06-26

Family has litigation

First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=6368328&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=LT3310(B) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.

1993-05-06 Application filed by Basf Lacke & Farben filed Critical Basf Lacke & Farben

1994-11-25 Publication of LTIP529A publication Critical patent/LTIP529A/xx

1995-06-26 Publication of LT3310B publication Critical patent/LT3310B/lt

Links

238000000576 coating method Methods 0.000 title claims abstract description 42
239000011248 coating agent Substances 0.000 title claims abstract description 34
239000011521 glass Substances 0.000 title claims abstract description 24
239000008199 coating composition Substances 0.000 title claims abstract description 10
239000007788 liquid Substances 0.000 title claims abstract description 6
239000000835 fiber Substances 0.000 title claims description 14
238000000034 method Methods 0.000 title claims description 12
239000005304 optical glass Substances 0.000 title claims description 7
239000004814 polyurethane Substances 0.000 claims abstract description 16
229920002635 polyurethane Polymers 0.000 claims abstract description 16
239000000178 monomer Substances 0.000 claims abstract description 14
HQYALQRYBUJWDH-UHFFFAOYSA-N trimethoxy(propyl)silane Chemical class CCC[Si](OC)(OC)OC HQYALQRYBUJWDH-UHFFFAOYSA-N 0.000 claims abstract description 11
SJECZPVISLOESU-UHFFFAOYSA-N 3-trimethoxysilylpropan-1-amine Chemical compound CO[Si](OC)(OC)CCCN SJECZPVISLOESU-UHFFFAOYSA-N 0.000 claims abstract description 9
DVYVMJLSUSGYMH-UHFFFAOYSA-N n-methyl-3-trimethoxysilylpropan-1-amine Chemical compound CNCCC[Si](OC)(OC)OC DVYVMJLSUSGYMH-UHFFFAOYSA-N 0.000 claims abstract description 9
239000000203 mixture Substances 0.000 claims description 65
230000005855 radiation Effects 0.000 claims description 13
RZVINYQDSSQUKO-UHFFFAOYSA-N 2-phenoxyethyl prop-2-enoate Chemical compound C=CC(=O)OCCOC1=CC=CC=C1 RZVINYQDSSQUKO-UHFFFAOYSA-N 0.000 claims description 5
239000003365 glass fiber Substances 0.000 claims description 5
XSQUKJJJFZCRTK-UHFFFAOYSA-N urea group Chemical group NC(=O)N XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 4
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 3
WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical group C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims description 3
238000005510 radiation hardening Methods 0.000 claims description 3
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 2
239000000654 additive Substances 0.000 claims description 2
239000000546 pharmaceutical excipient Substances 0.000 claims description 2
239000005977 Ethylene Substances 0.000 claims 1
239000000463 material Substances 0.000 abstract description 5
230000003287 optical effect Effects 0.000 abstract description 2
PHQOGHDTIVQXHL-UHFFFAOYSA-N n'-(3-trimethoxysilylpropyl)ethane-1,2-diamine Chemical compound CO[Si](OC)(OC)CCCNCCN PHQOGHDTIVQXHL-UHFFFAOYSA-N 0.000 abstract 1
150000003672 ureas Chemical group 0.000 abstract 1
-1 bis-phenol diethylene ester Chemical class 0.000 description 25
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 22
150000002596 lactones Chemical class 0.000 description 11
239000011230 binding agent Substances 0.000 description 10
150000002009 diols Chemical class 0.000 description 9
239000011152 fibreglass Substances 0.000 description 9
229920005862 polyol Polymers 0.000 description 9
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 8
239000004970 Chain extender Substances 0.000 description 7
125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 7
229920000570 polyether Polymers 0.000 description 7
150000003077 polyols Chemical class 0.000 description 7
238000012360 testing method Methods 0.000 description 7
BPSIOYPQMFLKFR-UHFFFAOYSA-N trimethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](OC)(OC)CCCOCC1CO1 BPSIOYPQMFLKFR-UHFFFAOYSA-N 0.000 description 7
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 6
125000002887 hydroxy group Chemical group [H]O* 0.000 description 6
239000012948 isocyanate Substances 0.000 description 6
125000004432 carbon atom Chemical group C* 0.000 description 5
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239000004721 Polyphenylene oxide Substances 0.000 description 4
125000002947 alkylene group Chemical group 0.000 description 4
239000013065 commercial product Substances 0.000 description 4
239000004922 lacquer Substances 0.000 description 4
229920000768 polyamine Polymers 0.000 description 4
229920000642 polymer Polymers 0.000 description 4
OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 3
NIXOWILDQLNWCW-UHFFFAOYSA-N Acrylic acid Chemical class OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
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238000010521 absorption reaction Methods 0.000 description 3
238000006243 chemical reaction Methods 0.000 description 3
150000004985 diamines Chemical class 0.000 description 3
KORSJDCBLAPZEQ-UHFFFAOYSA-N dicyclohexylmethane-4,4'-diisocyanate Chemical compound C1CC(N=C=O)CCC1CC1CCC(N=C=O)CC1 KORSJDCBLAPZEQ-UHFFFAOYSA-N 0.000 description 3
125000005442 diisocyanate group Chemical group 0.000 description 3
239000001257 hydrogen Substances 0.000 description 3
229910052739 hydrogen Inorganic materials 0.000 description 3
150000002513 isocyanates Chemical class 0.000 description 3
238000004519 manufacturing process Methods 0.000 description 3
150000001282 organosilanes Chemical class 0.000 description 3
229920000728 polyester Polymers 0.000 description 3
239000005056 polyisocyanate Substances 0.000 description 3
229920001228 polyisocyanate Polymers 0.000 description 3
239000000047 product Substances 0.000 description 3
239000002966 varnish Substances 0.000 description 3
PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 2
WYTZZXDRDKSJID-UHFFFAOYSA-N (3-aminopropyl)triethoxysilane Chemical compound CCO[Si](OCC)(OCC)CCCN WYTZZXDRDKSJID-UHFFFAOYSA-N 0.000 description 2
HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-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
KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 2
FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 2
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
239000005058 Isophorone diisocyanate Substances 0.000 description 2
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 2
ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 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 description 2
239000002253 acid Substances 0.000 description 2
239000002390 adhesive tape Substances 0.000 description 2
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
150000001412 amines Chemical class 0.000 description 2
IVRMZWNICZWHMI-UHFFFAOYSA-N azide group Chemical group [N-]=[N+]=[N-] IVRMZWNICZWHMI-UHFFFAOYSA-N 0.000 description 2
ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-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
239000012965 benzophenone Substances 0.000 description 2
WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
ZWWZGWFNRITNNP-UHFFFAOYSA-N carbonic acid;ethene Chemical class C=C.OC(O)=O ZWWZGWFNRITNNP-UHFFFAOYSA-N 0.000 description 2
238000004891 communication Methods 0.000 description 2
125000004386 diacrylate group Chemical group 0.000 description 2
150000002148 esters Chemical class 0.000 description 2
125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
125000002768 hydroxyalkyl group Chemical group 0.000 description 2
230000003993 interaction Effects 0.000 description 2
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 2
QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
238000005259 measurement Methods 0.000 description 2
QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 2
229910052753 mercury Inorganic materials 0.000 description 2
HEBKCHPVOIAQTA-UHFFFAOYSA-N meso ribitol Natural products OCC(O)C(O)C(O)CO HEBKCHPVOIAQTA-UHFFFAOYSA-N 0.000 description 2
XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
229920001451 polypropylene glycol Polymers 0.000 description 2
229920006295 polythiol Polymers 0.000 description 2
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 2
230000037452 priming Effects 0.000 description 2
239000011241 protective layer Substances 0.000 description 2
150000004756 silanes Chemical class 0.000 description 2
239000007858 starting material Substances 0.000 description 2
125000001424 substituent group Chemical group 0.000 description 2
238000006467 substitution reaction Methods 0.000 description 2
YRHRIQCWCFGUEQ-UHFFFAOYSA-N thioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3SC2=C1 YRHRIQCWCFGUEQ-UHFFFAOYSA-N 0.000 description 2
YUYCVXFAYWRXLS-UHFFFAOYSA-N trimethoxysilane Chemical compound CO[SiH](OC)OC YUYCVXFAYWRXLS-UHFFFAOYSA-N 0.000 description 2
229940096522 trimethylolpropane triacrylate Drugs 0.000 description 2
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
229920002554 vinyl polymer Polymers 0.000 description 2
ZWVMLYRJXORSEP-UHFFFAOYSA-N 1,2,6-Hexanetriol Chemical compound OCCCCC(O)CO ZWVMLYRJXORSEP-UHFFFAOYSA-N 0.000 description 1
VYMPLPIFKRHAAC-UHFFFAOYSA-N 1,2-ethanedithiol Chemical compound SCCS VYMPLPIFKRHAAC-UHFFFAOYSA-N 0.000 description 1
WAGRIKSHWXFXHV-UHFFFAOYSA-N 1-hydroxybutyl prop-2-enoate Chemical compound CCCC(O)OC(=O)C=C WAGRIKSHWXFXHV-UHFFFAOYSA-N 0.000 description 1
MIYFFZILCMZNRY-UHFFFAOYSA-N 1-hydroxypentyl prop-2-enoate Chemical compound CCCCC(O)OC(=O)C=C MIYFFZILCMZNRY-UHFFFAOYSA-N 0.000 description 1
DWFQYSNYIDKLCP-UHFFFAOYSA-N 1-methylcyclohexane-1,4-diamine Chemical compound CC1(N)CCC(N)CC1 DWFQYSNYIDKLCP-UHFFFAOYSA-N 0.000 description 1
VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 1
PIZHFBODNLEQBL-UHFFFAOYSA-N 2,2-diethoxy-1-phenylethanone Chemical compound CCOC(OCC)C(=O)C1=CC=CC=C1 PIZHFBODNLEQBL-UHFFFAOYSA-N 0.000 description 1
DPQHRXRAZHNGRU-UHFFFAOYSA-N 2,4,4-trimethylhexane-1,6-diamine Chemical class NCC(C)CC(C)(C)CCN DPQHRXRAZHNGRU-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
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
DPBJAVGHACCNRL-UHFFFAOYSA-N 2-(dimethylamino)ethyl prop-2-enoate Chemical compound CN(C)CCOC(=O)C=C DPBJAVGHACCNRL-UHFFFAOYSA-N 0.000 description 1
BVDQHCUOVIQIEJ-UHFFFAOYSA-N 2-(hydroxymethyl)-2-methylpropane-1,3-diol;propane-1,2,3-triol Chemical compound OCC(O)CO.OCC(C)(CO)CO BVDQHCUOVIQIEJ-UHFFFAOYSA-N 0.000 description 1
SZSSMFVYZRQGIM-UHFFFAOYSA-N 2-(hydroxymethyl)-2-propylpropane-1,3-diol Chemical compound CCCC(CO)(CO)CO SZSSMFVYZRQGIM-UHFFFAOYSA-N 0.000 description 1
HEXHLHNCJVXPNU-UHFFFAOYSA-N 2-(trimethoxysilylmethyl)butane-1,4-diamine Chemical compound CO[Si](OC)(OC)CC(CN)CCN HEXHLHNCJVXPNU-UHFFFAOYSA-N 0.000 description 1
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 description 1
PTJWCLYPVFJWMP-UHFFFAOYSA-N 2-[[3-hydroxy-2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)COCC(CO)(CO)CO PTJWCLYPVFJWMP-UHFFFAOYSA-N 0.000 description 1
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LOJSNUXAIXEBPJ-UHFFFAOYSA-N 2-chloro-2-(1,1,2,2,3-pentachlorohexyl)propanedioic acid Chemical class CCCC(Cl)C(Cl)(Cl)C(Cl)(Cl)C(Cl)(C(O)=O)C(O)=O LOJSNUXAIXEBPJ-UHFFFAOYSA-N 0.000 description 1
ZAXCZCOUDLENMH-UHFFFAOYSA-N 3,3,3-tetramine Chemical compound NCCCNCCCNCCCN ZAXCZCOUDLENMH-UHFFFAOYSA-N 0.000 description 1
QKJWEMFCEHDWQH-UHFFFAOYSA-N 3,3-bis(hydroxymethyl)butane-1,1,4-triol Chemical compound C(O)C(CC(O)O)(CO)CO QKJWEMFCEHDWQH-UHFFFAOYSA-N 0.000 description 1
RNLHGQLZWXBQNY-UHFFFAOYSA-N 3-(aminomethyl)-3,5,5-trimethylcyclohexan-1-amine Chemical compound CC1(C)CC(N)CC(C)(CN)C1 RNLHGQLZWXBQNY-UHFFFAOYSA-N 0.000 description 1
POTQBGGWSWSMCX-UHFFFAOYSA-N 3-[2-(3-aminopropoxy)ethoxy]propan-1-amine Chemical compound NCCCOCCOCCCN POTQBGGWSWSMCX-UHFFFAOYSA-N 0.000 description 1
YOOSAIJKYCBPFW-UHFFFAOYSA-N 3-[4-(3-aminopropoxy)butoxy]propan-1-amine Chemical compound NCCCOCCCCOCCCN YOOSAIJKYCBPFW-UHFFFAOYSA-N 0.000 description 1
YAGKYVUYEIAZDQ-UHFFFAOYSA-N 3-[5-(3-aminopropoxy)-3-methylpentoxy]propan-1-amine Chemical compound NCCCOCCC(C)CCOCCCN YAGKYVUYEIAZDQ-UHFFFAOYSA-N 0.000 description 1
QZPSOSOOLFHYRR-UHFFFAOYSA-N 3-hydroxypropyl prop-2-enoate Chemical compound OCCCOC(=O)C=C QZPSOSOOLFHYRR-UHFFFAOYSA-N 0.000 description 1
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UUEWCQRISZBELL-UHFFFAOYSA-N 3-trimethoxysilylpropane-1-thiol Chemical compound CO[Si](OC)(OC)CCCS UUEWCQRISZBELL-UHFFFAOYSA-N 0.000 description 1
XDLMVUHYZWKMMD-UHFFFAOYSA-N 3-trimethoxysilylpropyl 2-methylprop-2-enoate Chemical compound CO[Si](OC)(OC)CCCOC(=O)C(C)=C XDLMVUHYZWKMMD-UHFFFAOYSA-N 0.000 description 1
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ORLQHILJRHBSAY-UHFFFAOYSA-N [1-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1(CO)CCCCC1 ORLQHILJRHBSAY-UHFFFAOYSA-N 0.000 description 1
CQHKDHVZYZUZMJ-UHFFFAOYSA-N [2,2-bis(hydroxymethyl)-3-prop-2-enoyloxypropyl] prop-2-enoate Chemical compound C=CC(=O)OCC(CO)(CO)COC(=O)C=C CQHKDHVZYZUZMJ-UHFFFAOYSA-N 0.000 description 1
238000005299 abrasion Methods 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-M acrylate group Chemical group C(C=C)(=O)[O-] NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
235000011037 adipic acid Nutrition 0.000 description 1
239000001361 adipic acid Substances 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
125000003545 alkoxy group Chemical group 0.000 description 1
125000000217 alkyl group Chemical group 0.000 description 1
LHIJANUOQQMGNT-UHFFFAOYSA-N aminoethylethanolamine Chemical compound NCCNCCO LHIJANUOQQMGNT-UHFFFAOYSA-N 0.000 description 1
150000008064 anhydrides Chemical class 0.000 description 1
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 1
150000004056 anthraquinones Chemical class 0.000 description 1
150000001491 aromatic compounds Chemical class 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
230000000712 assembly Effects 0.000 description 1
238000000429 assembly Methods 0.000 description 1
229960002130 benzoin Drugs 0.000 description 1
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
239000004305 biphenyl Substances 0.000 description 1
LUZRKMGMNFOSFZ-UHFFFAOYSA-N but-3-enyl(triethoxy)silane Chemical compound CCO[Si](OCC)(OCC)CCC=C LUZRKMGMNFOSFZ-UHFFFAOYSA-N 0.000 description 1
CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 1
WQAQPCDUOCURKW-UHFFFAOYSA-N butanethiol Chemical compound CCCCS WQAQPCDUOCURKW-UHFFFAOYSA-N 0.000 description 1
BELZJFWUNQWBES-UHFFFAOYSA-N caldopentamine Chemical compound NCCCNCCCNCCCNCCCN BELZJFWUNQWBES-UHFFFAOYSA-N 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
150000004649 carbonic acid derivatives Chemical class 0.000 description 1
150000001875 compounds Chemical class 0.000 description 1
238000005859 coupling reaction Methods 0.000 description 1
125000000753 cycloalkyl group Chemical group 0.000 description 1
125000002993 cycloalkylene group Chemical group 0.000 description 1
QSAWQNUELGIYBC-UHFFFAOYSA-N cyclohexane-1,2-dicarboxylic acid Chemical compound OC(=O)C1CCCCC1C(O)=O QSAWQNUELGIYBC-UHFFFAOYSA-N 0.000 description 1
HEBKCHPVOIAQTA-NGQZWQHPSA-N d-xylitol Chemical compound OC[C@H](O)C(O)[C@H](O)CO HEBKCHPVOIAQTA-NGQZWQHPSA-N 0.000 description 1
230000006866 deterioration Effects 0.000 description 1
150000001991 dicarboxylic acids Chemical class 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
239000000539 dimer Substances 0.000 description 1
USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Natural products C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 1
238000007598 dipping method Methods 0.000 description 1
SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
150000004662 dithiols Chemical class 0.000 description 1
239000000428 dust Substances 0.000 description 1
230000000694 effects Effects 0.000 description 1
238000005516 engineering process Methods 0.000 description 1
UNXHWFMMPAWVPI-ZXZARUISSA-N erythritol Chemical compound OC[C@H](O)[C@H](O)CO UNXHWFMMPAWVPI-ZXZARUISSA-N 0.000 description 1
125000001033 ether group Chemical group 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
150000002191 fatty alcohols Chemical class 0.000 description 1
239000005357 flat glass Substances 0.000 description 1
238000009472 formulation Methods 0.000 description 1
125000000524 functional group Chemical group 0.000 description 1
230000009477 glass transition Effects 0.000 description 1
229930182478 glucoside Natural products 0.000 description 1
150000002334 glycols Chemical class 0.000 description 1
235000019382 gum benzoic Nutrition 0.000 description 1
RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
TZMQHOJDDMFGQX-UHFFFAOYSA-N hexane-1,1,1-triol Chemical compound CCCCCC(O)(O)O TZMQHOJDDMFGQX-UHFFFAOYSA-N 0.000 description 1
ACCCMOQWYVYDOT-UHFFFAOYSA-N hexane-1,1-diol Chemical compound CCCCCC(O)O ACCCMOQWYVYDOT-UHFFFAOYSA-N 0.000 description 1
ALPIESLRVWNLAX-UHFFFAOYSA-N hexane-1,1-dithiol Chemical compound CCCCCC(S)S ALPIESLRVWNLAX-UHFFFAOYSA-N 0.000 description 1
XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
229920001519 homopolymer Polymers 0.000 description 1
239000000976 ink Substances 0.000 description 1
LDHQCZJRKDOVOX-IHWYPQMZSA-N isocrotonic acid Chemical class C\C=C/C(O)=O LDHQCZJRKDOVOX-IHWYPQMZSA-N 0.000 description 1
GKQPCPXONLDCMU-CCEZHUSRSA-N lacidipine Chemical compound CCOC(=O)C1=C(C)NC(C)=C(C(=O)OCC)C1C1=CC=CC=C1\C=C\C(=O)OC(C)(C)C GKQPCPXONLDCMU-CCEZHUSRSA-N 0.000 description 1
239000010410 layer Substances 0.000 description 1
238000005461 lubrication Methods 0.000 description 1
239000000594 mannitol Substances 0.000 description 1
235000010355 mannitol Nutrition 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
125000005395 methacrylic acid group Chemical group 0.000 description 1
KMBPCQSCMCEPMU-UHFFFAOYSA-N n'-(3-aminopropyl)-n'-methylpropane-1,3-diamine Chemical compound NCCCN(C)CCCN KMBPCQSCMCEPMU-UHFFFAOYSA-N 0.000 description 1
ITZPOSYADVYECJ-UHFFFAOYSA-N n'-cyclohexylpropane-1,3-diamine Chemical compound NCCCNC1CCCCC1 ITZPOSYADVYECJ-UHFFFAOYSA-N 0.000 description 1
QHJABUZHRJTCAR-UHFFFAOYSA-N n'-methylpropane-1,3-diamine Chemical compound CNCCCN QHJABUZHRJTCAR-UHFFFAOYSA-N 0.000 description 1
AUHCUXSNXHQCFS-UHFFFAOYSA-N n-benzyl-n-ethenyl-3-trimethoxysilylpropan-1-amine Chemical compound CO[Si](OC)(OC)CCCN(C=C)CC1=CC=CC=C1 AUHCUXSNXHQCFS-UHFFFAOYSA-N 0.000 description 1
SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
229940117969 neopentyl glycol Drugs 0.000 description 1
150000002825 nitriles Chemical class 0.000 description 1
BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 1
229940065472 octyl acrylate Drugs 0.000 description 1
150000002894 organic compounds Chemical class 0.000 description 1
125000004430 oxygen atom Chemical group O* 0.000 description 1
239000003973 paint Substances 0.000 description 1
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
UWJJYHHHVWZFEP-UHFFFAOYSA-N pentane-1,1-diol Chemical compound CCCCC(O)O UWJJYHHHVWZFEP-UHFFFAOYSA-N 0.000 description 1
NCHIGRUKPIGGQF-UHFFFAOYSA-N pentane-1,1-dithiol Chemical compound CCCCC(S)S NCHIGRUKPIGGQF-UHFFFAOYSA-N 0.000 description 1
239000004014 plasticizer Substances 0.000 description 1
229920000058 polyacrylate Polymers 0.000 description 1
229920001281 polyalkylene Polymers 0.000 description 1
229920001610 polycaprolactone Polymers 0.000 description 1
239000004632 polycaprolactone Substances 0.000 description 1
229920000573 polyethylene Polymers 0.000 description 1
238000006116 polymerization reaction Methods 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
238000007639 printing Methods 0.000 description 1
ZJLMKPKYJBQJNH-UHFFFAOYSA-N propane-1,3-dithiol Chemical compound SCCCS ZJLMKPKYJBQJNH-UHFFFAOYSA-N 0.000 description 1
KRIOVPPHQSLHCZ-UHFFFAOYSA-N propiophenone Chemical compound CCC(=O)C1=CC=CC=C1 KRIOVPPHQSLHCZ-UHFFFAOYSA-N 0.000 description 1
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 description 1
KIDHWZJUCRJVML-UHFFFAOYSA-N putrescine Chemical class NCCCCN KIDHWZJUCRJVML-UHFFFAOYSA-N 0.000 description 1
229920013730 reactive polymer Polymers 0.000 description 1
239000011435 rock Substances 0.000 description 1
238000005096 rolling process Methods 0.000 description 1
229910000077 silane Inorganic materials 0.000 description 1
229910052710 silicon Inorganic materials 0.000 description 1
239000010703 silicon Substances 0.000 description 1
239000002356 single layer Substances 0.000 description 1
239000000600 sorbitol Substances 0.000 description 1
235000010356 sorbitol Nutrition 0.000 description 1
238000005507 spraying Methods 0.000 description 1
238000003860 storage Methods 0.000 description 1
239000000758 substrate Substances 0.000 description 1
239000005720 sucrose Substances 0.000 description 1
PXQLVRUNWNTZOS-UHFFFAOYSA-N sulfanyl Chemical class [SH] PXQLVRUNWNTZOS-UHFFFAOYSA-N 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
230000007704 transition Effects 0.000 description 1
ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 1
150000004072 triols Chemical class 0.000 description 1
MBYLVOKEDDQJDY-UHFFFAOYSA-N tris(2-aminoethyl)amine Chemical compound NCCN(CCN)CCN MBYLVOKEDDQJDY-UHFFFAOYSA-N 0.000 description 1
239000000811 xylitol Substances 0.000 description 1
HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 description 1
235000010447 xylitol Nutrition 0.000 description 1
229960002675 xylitol Drugs 0.000 description 1
PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical class O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- 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
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D175/00—Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
- C09D175/04—Polyurethanes
- C09D175/14—Polyurethanes having carbon-to-carbon unsaturated bonds
- C09D175/16—Polyurethanes having carbon-to-carbon unsaturated bonds having terminal carbon-to-carbon unsaturated bonds

Landscapes

Chemical & Material Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Organic Chemistry (AREA)
Wood Science & Technology (AREA)
General Life Sciences & Earth Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
General Chemical & Material Sciences (AREA)
Geochemistry & Mineralogy (AREA)
Paints Or Removers (AREA)
Surface Treatment Of Glass Fibres Or Filaments (AREA)
Polymerisation Methods In General (AREA)
Optical Fibers, Optical Fiber Cores, And Optical Fiber Bundles (AREA)
Macromonomer-Based Addition Polymer (AREA)

LTIP529A 1988-12-02 1993-05-06 Liquid, radiation-cured coating composition for glass surfaces, process for coating, optical glass fibre LT3310B (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE3840644A DE3840644A1 (de)	1988-12-02	1988-12-02	Fluessige, strahlenhaertbare ueberzugsmasse fuer die beschichtung von glasoberflaechen

Publications (2)

Publication Number	Publication Date
LTIP529A LTIP529A (en)	1994-11-25
LT3310B true LT3310B (en)	1995-06-26

Family

ID=6368328

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
LTIP529A LT3310B (en)	1988-12-02	1993-05-06	Liquid, radiation-cured coating composition for glass surfaces, process for coating, optical glass fibre

Country Status (14)

Country	Link
EP (1)	EP0446222B1 (da)
JP (1)	JPH0776120B2 (da)
KR (1)	KR930006328B1 (da)
AU (1)	AU624196B2 (da)
BR (1)	BR8907803A (da)
CA (1)	CA2004407A1 (da)
DE (2)	DE3840644A1 (da)
DK (1)	DK166079C (da)
ES (1)	ES2039097T3 (da)
FI (1)	FI96432C (da)
LT (1)	LT3310B (da)
LV (1)	LV10766A (da)
MD (1)	MD940077A (da)
WO (1)	WO1990006289A1 (da)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3914411A1 (de)	1989-04-29	1990-11-15	Basf Lacke & Farben	Fluessige, strahlenhaertbare ueberzugsmasse fuer die beschichtung von glasoberflaechen
US5149592A (en) *	1990-05-09	1992-09-22	Avery Dennison Corporation	Ultraviolet radiation curable clearcoat
DE4139127A1 (de) *	1991-11-28	1993-06-03	Basf Lacke & Farben	Fluessige, strahlenhaertbare ueberzugsmasse fuer die beschichtung von glasoberflaechen
CA2082614A1 (en) *	1992-04-24	1993-10-25	Paul J. Shustack	Organic solvent and water resistant, thermally, oxidatively and hydrolytically stable radiation-curable coatings for optical fibers, optical fibers coated therewith and processes for making same
CA2107448A1 (en) *	1992-11-13	1994-05-14	Lee Landis Blyler, Jr.	Optical transmission media having enhanced strength retention capabilities
DE19535936A1 (de) *	1995-09-27	1997-04-03	Basf Lacke & Farben	Acryliertes Polyetherpolyol und dessen Verwendung für strahlenhärtbare Formulierungen
DE19535935A1 (de) *	1995-09-27	1997-04-03	Basf Lacke & Farben	Strahlenhärtbarer Überzug
US6023547A (en) *	1997-06-09	2000-02-08	Dsm N.V.	Radiation curable composition comprising a urethane oligomer having a polyester backbone
US6391936B1 (en)	1997-12-22	2002-05-21	Dsm N.V.	Radiation-curable oligomers radiation-curable compositions, coated optical glass fibers, and ribbon assemblies
US6797746B2 (en) *	1998-12-22	2004-09-28	Vidriera Monterrey, S.A. De C.V.	Ultraviolet radiation curable ink composition and a process for its application on glass substrates
US6171698B1 (en) *	1999-08-19	2001-01-09	Alcatel	Radiation curable coating composition for optical fibers and optical fibers coated thereby
DE10049153A1 (de) *	2000-09-27	2002-04-11	Degussa	Farbe, Lack, Schadstoffe, Bioorganismen, Öl, Wasser, und/oder Schmutz abweisende Beschichtung

Citations (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP0149741A1 (en)	1983-11-10	1985-07-31	DeSOTO, INC.	Liquid radiation-curable coating compositions and optical glass fibers coated therewith
EP0114982B1 (en)	1982-12-28	1987-06-10	DeSOTO, INC.	Topcoats for buffer-coated optical fiber
EP0250631A1 (en)	1986-07-02	1988-01-07	DeSOTO, INC.	Ultraviolet curable buffer coatings for optical fiber
JPH0224480A (ja)	1988-07-13	1990-01-26	Toyo Denki Tsushin Kogyo Kk	シールドマシンの推進装置
JPH0513885A (ja)	1991-07-04	1993-01-22	Mitsubishi Electric Corp	可視光半導体レーザの製造方法

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS57209855A (en) *	1981-06-17	1982-12-23	Unitika Ltd	Water-based sizing agent for glass fiber
US4932750A (en) *	1982-12-09	1990-06-12	Desoto, Inc.	Single-coated optical fiber
JPS6083907A (ja) *	1983-10-14	1985-05-13	Nitto Electric Ind Co Ltd	光学ガラスフアイバ用被覆材料
DE3914411A1 (de) *	1989-04-29	1990-11-15	Basf Lacke & Farben	Fluessige, strahlenhaertbare ueberzugsmasse fuer die beschichtung von glasoberflaechen

1988
- 1988-12-02 DE DE3840644A patent/DE3840644A1/de not_active Ceased
1989
- 1989-11-17 JP JP1511562A patent/JPH0776120B2/ja not_active Expired - Lifetime
- 1989-11-17 DE DE8989912446T patent/DE58903477D1/de not_active Revoked
- 1989-11-17 BR BR898907803A patent/BR8907803A/pt not_active Application Discontinuation
- 1989-11-17 KR KR1019900701680A patent/KR930006328B1/ko not_active Expired - Fee Related
- 1989-11-17 ES ES198989912446T patent/ES2039097T3/es not_active Expired - Lifetime
- 1989-11-17 EP EP89912446A patent/EP0446222B1/de not_active Revoked
- 1989-11-17 WO PCT/EP1989/001382 patent/WO1990006289A1/de not_active Ceased
- 1989-11-17 AU AU45121/89A patent/AU624196B2/en not_active Ceased
- 1989-12-01 CA CA002004407A patent/CA2004407A1/en not_active Abandoned
1991
- 1991-05-31 FI FI912625A patent/FI96432C/fi not_active IP Right Cessation
- 1991-05-31 DK DK103991A patent/DK166079C/da active
1993
- 1993-05-06 LT LTIP529A patent/LT3310B/lt not_active IP Right Cessation
- 1993-05-27 LV LV930429A patent/LV10766A/xx unknown
1994
- 1994-04-05 MD MD94-0077A patent/MD940077A/ro unknown

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP0114982B1 (en)	1982-12-28	1987-06-10	DeSOTO, INC.	Topcoats for buffer-coated optical fiber
EP0149741A1 (en)	1983-11-10	1985-07-31	DeSOTO, INC.	Liquid radiation-curable coating compositions and optical glass fibers coated therewith
EP0250631A1 (en)	1986-07-02	1988-01-07	DeSOTO, INC.	Ultraviolet curable buffer coatings for optical fiber
JPH0224480A (ja)	1988-07-13	1990-01-26	Toyo Denki Tsushin Kogyo Kk	シールドマシンの推進装置
JPH0513885A (ja)	1991-07-04	1993-01-22	Mitsubishi Electric Corp	可視光半導体レーザの製造方法

Also Published As

Publication number	Publication date
FI96432B (fi)	1996-03-15
KR930006328B1 (ko)	1993-07-14
WO1990006289A1 (de)	1990-06-14
DE3840644A1 (de)	1990-06-07
FI912625A0 (fi)	1991-05-31
KR910700207A (ko)	1991-03-14
DK103991D0 (da)	1991-05-31
LV10766A (lv)	1995-08-20
BR8907803A (pt)	1991-08-27
EP0446222A1 (de)	1991-09-18
JPH03505197A (ja)	1991-11-14
AU4512189A (en)	1990-06-26
EP0446222B1 (de)	1993-02-03
LTIP529A (en)	1994-11-25
DE58903477D1 (de)	1993-03-18
FI96432C (fi)	1996-06-25
AU624196B2 (en)	1992-06-04
DK166079C (da)	1993-08-02
MD940077A (ro)	1996-01-31
CA2004407A1 (en)	1990-06-02
DK103991A (da)	1991-07-18
DK166079B (da)	1993-03-08
ES2039097T3 (es)	1993-08-16
JPH0776120B2 (ja)	1995-08-16

Legal Events

Date	Code	Title	Description
1996-12-27	MM9A	Lapsed patents	Effective date: 19960506

Publication	Publication Date	Title
LT3330B (en)	1995-07-25	Liquid, radiation-cured coating composition for glass surfaces
JP3686082B2 (ja)	2005-08-24	ガラスの接着力保持のための塗料システム
LT3310B (en)	1995-06-26	Liquid, radiation-cured coating composition for glass surfaces, process for coating, optical glass fibre
JPH09509642A (ja)	1997-09-30	ガラスの強度保持のための塗料システム
US7105583B2 (en)	2006-09-12	Radiation-curable compositions for optical fiber coating materials
US5461691A (en)	1995-10-24	Liquid, radiation-curable coating composition for coating glass surfaces
WO2019026356A1 (ja)	2019-02-07	光ファイバ及び光ファイバの製造方法
EP0149741B1 (en)	1989-08-09	Liquid radiation-curable coating compositions and optical glass fibers coated therewith
RU2320590C2 (ru)	2008-03-27	Оптическое волокно с отвержденным полимерным покрытием
JP2509409B2 (ja)	1996-06-19	ガラス表面を被覆するための放射線硬化可能なオリゴマ―の製造法
US20030119998A1 (en)	2003-06-26	Free radical-curable composition for optical fiber coating materials
KR100626509B1 (ko)	2006-09-20	광섬유 코팅재용 방사선-경화가능한 조성물