Claims
- 1. A radiation-curable coating composition for an optical fiber comprising a reactive functionality-terminated urethane oligomer, wherein said oligomer comprises the reaction product of (i) a semi-crystalline polyol having a molecular weight of from about 200 to about 1000, and (ii) a non-crystalline polyol in the mole ratio of semi-crystalline polyol to non-crystalline polyol of between about 10:1 and 1:10, wherein said non-crystalline polyol is selected from the group consisting of polyether polyols, polyester polyols, polydimethylsiloxane, polystyrene, polycarbonates, acrylated acrylics, or combinations thereof, (iii) at least one isocyanate, and (iv) an endcapping compound capable of supplying the reactive functionality terminus, and wherein the stoichiometry is selected such that, on average, about 50% or more of the oligomer contains a non-crystalline polyol, said coating composition having a freezing temperature below 0° C.
- 2. The composition of claim 1, wherein said composition has a melting temperature below 0° C.
- 3. The composition of claim 1, wherein the non-crystalline polyol has a molecular weight of from about 900 to about 10,000, and an hydroxyl number of from about 5 to about 60.
- 4. The composition of claim 1, wherein said semi-crystalline polyol is poly(tetramethylene oxide).
- 5. The composition of claim 1, wherein said non-crystalline polyol is selected from the group consisting of polypropylene glycol, polytetrahydrofuran-methyltetrahydrofuran, polyester or combinations thereof.
- 6. The composition of claim 1, wherein the mole ratio of semi-crystalline polyol to non-crystalline polyol is from about 3:1 to about 1:6.
- 7. The composition of claim 1, wherein said isocyanate is selected from the group consisting of an aromatic isocyanate, an aliphatic isocyanate and mixtures thereof.
- 8. The composition of claim 1, wherein said composition further comprises at least one reactive diluent, said reactive diluent including at least one group capable of reacting with the reactive functionality terminus of the urethane oligomer and a photoinitiator.
- 9. The composition of claim 1, wherein said endcapping compound is selected from the group consisting of acrylate, methacrylate, styrene, vinylether, vinyl ester, N-substituted acrylamide, N-vinyl amide, maleate esters, and fumarate esters.
- 10. The composition of claim 1, wherein said composition further comprises at least one adhesion promoter.
- 11. The coating composition of any one of claims 1, 2, 3 or 7, wherein said composition is an inner primary coating, said composition, after cure, having a tensile modulus of from about 0.1 to about 10 MPa.
- 12. The coating composition of any one of claims 1, 2, 3 or 7, wherein said composition is an outer primary coating.
- 13. A radiation-curable coating composition for an optical fiber comprising a reactive functionality-terminated urethane oligomer, wherein said oligomer comprises the reaction product of (i) a semi-crystalline polyol having a molecular weight of from about 200 to about 1000, and (ii) a non-crystalline polyol in the mole ratio of semi-crystalline polyol to non-crystalline polyol of at least about 1:1, wherein said non-crystalline polyol is selected from the group consisting of polyether polyols, polyester polyols, polydimethylsiloxane, polystyrene, polycarbonates, acrylated acrylics, or combinations thereof, (iii) at least one isocyanate, and (iv) an endcapping compound capable of supplying the reactive functionality terminus, said coating composition having a freezing temperature below 0° C.
- 14. A radiation-curable coating composition for an optical fiber comprising a reactive functionality-terminated urethane oligomer, wherein said oligomer comprises the reaction product of (i) a semi-crystalline polyol, and (ii) a non-crystalline polyol in the ratio of semi-crystalline polyol to non-crystalline polyol of at least about 1:1, wherein said non-crystalline polyol is selected from the group consisting of polyether polyols, polyester polyols, polydimethylsiloxane, polystyrene, polycarbonates, acrylated acrylics, or combinations thereof, (iii) at least one isocyanate, and (iv) an endcapping compound capable of supplying the reactive functionality terminus, wherein the semi-crystalline polyol has a molecular weight of from about 200 to about 1,000, and the non-crystalline polyol has a molecular weight of from about 900 to about 10,000, and an hydroxyl number of from about 5 to about 60, said coating composition having a freezing temperature below 0° C. and a melt temperature below 0° C.
- 15. A coated optical fiber having an inner and outer primary coating and optionally an ink coating, wherein at least one of the coatings is a cured composition according to any one of claims 1, 13 or 14.
- 16. A ribbon comprising coated and optionally inked optical fibers, bonded or covered by a matrix material wherein the matrix material is a cured composition according to any one of claims 1, 13 or 14.
- 17. A reactive functionality-terminated urethane oligomer, wherein said oligomer comprises the reaction product of (i) a semi-crystalline polyol having a molecular weight of from about 200 to about 1000, and (ii) a non-crystalline polyol in the ratio of semi-crystalline polyol to non-crystalline polyol of at least about 1:1, wherein said non-crystalline polyol is selected from the group consisting of polyether polyols, polyester polyols, polydimethylsiloxane, polystyrene, polycarbonates, acrylated acrylics, or combinations thereof, (iii) at least one isocyanate, and (iv) an endcapping compound capable of supplying the reactive functionality terminus, said oligomer having a freezing temperature below 0° C.
- 18. A reactive functionality-terminated urethane oligomer, wherein said oligomer comprises the reaction product of (i) a semi-crystalline polyol having a molecular weight of from about 200 to about 1000, and (ii) a non-crystalline polyol in the ratio of semi-crystalline polyol to non-crystalline polyol of between about 10:1 to about 1:10, wherein said non-crystalline polyol is selected from the group consisting of polyether polyols, polyester polyols, polydimethylsiloxane, polystyrene, polycarbonates, acrylated acrylics, or combinations thereof, (iii) at least one isocyanate, and (iv) an endcapping compound capable of supplying the reactive functionality terminus, said oligomer having a freezing temperature below 0° C.
- 19. The oligomer of any one of claims 17 or 18, wherein said oligomer has a melt temperature below 0° C.
- 20. The oligomer of claim 19, wherein the non-crystalline polyol has a molecular weight of from about 900 to about 10,000, and an hydroxyl number of from about 5 to about 60.
- 21. The oligomer of claim 20, wherein said semi-crystalline polyol is poly(tetramethylene oxide).
- 22. The oligomer of claim 20, wherein said non-crystalline polyol is polypropylene glycol.
- 23. The coating composition of any of claims 1, 13 or 14, wherein said composition has no observable freezing temperature and no observable melting temperature above about −60° C.
Parent Case Info
This application claims the benefit of U.S. Provisional Application No. 60/259,023, filed Dec. 29, 2000.
US Referenced Citations (88)
Foreign Referenced Citations (5)
Number |
Date |
Country |
0 228 854 |
Jul 1987 |
EP |
0 780 712 |
Jun 1997 |
EP |
1 134 201 |
Sep 2001 |
EP |
60-176953 |
Sep 1985 |
JP |
6354416 |
Sep 1988 |
JP |
Non-Patent Literature Citations (2)
Entry |
“Effect Of Chemical Environments On UV Curable Optical Fiber Coatings,” by Chander P. Chawla et al., International Wire & Cable Symposium Proceedings 1991, pp. 141-148. |
“Studies of Structure and Properties of Photocrosslinked Polyurethane Acrylates,” by Jie Dai et al., pp. 174-184; 1991. |
Provisional Applications (1)
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Number |
Date |
Country |
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60/259023 |
Dec 2000 |
US |