IP Library Granted Patent US 6,887,918
Granted Patent B2
US 6,887,918 · App. 10/265,617 · Granted May 3, 2005

Formulation of UV-curable coatings for optical fiber for a fast cure

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Quick Facts
Patent No.
US 6,887,918
App. No.
10/265,617
Granted
May 3, 2005
Kind
B2
Abstract

A fast-curing, low viscosity composition for coating an optical waveguide, more specifically, an optical fiber, and optical fibers coated therewith are disclosed. The coating composition is a radiation curable composition containing: a radiation curable oligomer, a free radical photoinitiator, and a mixture of reactive diluents including a low molecular weight (meth)acrylate having tri-, tetra-, penta- or higher functionality.

Claims (20)

1. An optical waveguide coated with a liquid, radiation-curable composition, said composition comprising (a) a radiation-curable oligomer, (b) a free radical photoinitiator, and (c) a mixture of reactive diluents comprising (i) at least one mono- or difunctional reactive diluent and (ii) at least one polyfunctional reactive diluent having at least four (meth)acrylate functionalities.

2. An optical waveguide coated with a cured composition, said cured composition composing (a) a radiation-curable oligomer, (b) a free radical photoinitiator, and (c) a mixture of reactive diluents comprising (i) at least one mono- or difunctional reactive diluent and (ii) at least one polyfunctional reactive diluent having at least four (meth)acrylate functionalities.

3. The optical waveguide of claim 2 , wherein the thickness of the cured composition is from about 20 to 35 microns.

4. A method of coating an optical waveguide with a liquid, radiation-curable composition, said method comprising the steps of:

(a) contacting said optical waveguide with said liquid, radiation-curable composition; and

(b) curing said liquid, radiation-curable composition,

wherein said liquid, radiation-curable composition comprises (a) a radiation-curable oligomer, (b) a free radical photoinitiator, and (c) a mixture of reactive diluents comprising (i) at least one mono- or difunctional reactive diluent and (ii) at least one polyfunctional reactive diluent having at least four (meth)acrylate functionalities.

5. The optical waveguide of claim 1 , wherein said radiation-curable oligomer (a) is a urethane acrylate oligomer that has a backbone selected from the group consisting of a polyester backbone, a polyether backbone, and a polycarbonate backbone.

6. The optical waveguide of claim 1 , wherein said radiation-curable oligomer (a) is a urethane acrylate oligomer that has an average molecular weight (MW) range of from about 5,000 to about 25,000.

7. The optical waveguide of claim 1 , wherein said free radical photoinitiator (b) is present in an amount of up to 6% by total weight of said liquid, radiation-curable composition.

8. The optical waveguide of claim 1 , wherein said free radical photoinitiator (b) is selected from the group consisting of acyl phosphine oxide, 2,4,6-trimethylbenzoyldipbenyl-phosphine oxide, bis (2,6-dimethoxybenzoyl)-2,4,4-trimethylpentylphosphine oxide, hydroxycyclohexylphenylketone, hyroxymethylphenylpropanone, dimethoxyphenylacetophenone, 2-methyl-1-[4-(methyl thio)-phenyl]-2-morpholinopropanone-1,1-(4-isopropylphenyl)-2-hydroxy-2-methylpropan-1-one, 1-(4-dodecyl-phenyl)-2-hydroxy-2-methylpropan-1-one, 4-(2-hydroxyethoxy)phenyl-2(2-hydroxy-2-propyl)-ketone, diethoxyphenyl acetophenone, 2,4,6 trimethylbenzoyl diphenylphosphone, and mixtures thereof.

9. The optical waveguide of claim 1 , wherein said at least one mono- or difunctional reactive diluent (c)(i) composes a monofunctional acrylate or diacrylate.

10. The optical waveguide of claim 9 , wherein the weight ratio of said at least one mono- or difunctional reactive diluent (c)(i) to said at least one polyfunctional reactive diluent (c)(ii) is at least 3 to 1.

11. The optical wavegwde of claim 1 , wherein said at least one mono- or difunctional reactive diluent (c)(i) is selected from the group consisting of tridecyl acrylate, 1,6-hexanediol diacrylate, 1,4-butanediol diacrylate, ethylene glycol diacrylate, diethylene glycol diacrylate, tetraethylene glycol diacrylate, tripropylene glycol diacrylate, neopentyl glycol diacrylate, 1,4-butanediol dimethacrylate, poly(butanediol) diacrylate, tetrathylene glycol dimethacrylatc, 1,3-butylene glycol diacrylate, tetraethylene glycol diacrylate, triisopropylene glycol diacrylate, triisopzopylenc glycol diacrylate, ethoxylated bisphenol-A diacrylate, isobornyl acrylate, and N-vinyl caprolactam.

12. The optical waveguide of claim 1 , wherein the amount of said at least one polyfunctional reactive diluent (c)(ii) is from about 0.5 to 3 wt % by total weight of said liquid, radiation-curable composition.

13. The optical waveguide of claim 12 , wherein said liquid, radiation-curable composition has a viscosity on the order of magnitude of about 10 3 cP at 45-50° C.

14. The optical waveguide of claim 13 , wherein said liquid, radiation-curable composition has a viscosity of from about 2×10 3 to about 8×10 3 cP at room temperature.

15. The optical waveguide of claim 1 , wherein said radiation-curable oligomer (a) is a urethane acrylate oligomer that is the reaction product of a polyol selected from the group consisting of ethylene glycol, propylene glycol, tripropylene glycol, 1,3-butanediol, 1,4-butanediol, neopentyl glycol, 1,6-hexanediol, 1,9-nonanediol, 1,10-decanediol, castor oil, coconut oil, 1-monomyristin, 2-monomyristin, 1-monopalmitin, 2-monopalmitin, 1-monostearin, 2-monostearin, 1-monoolein, 2-monoolein, 9,10-dioxystearic acid, 12-hydroxyricinolcyl alcohol, 12-hydroxystearyl alcohol, 1,16-hexadecanediol, 1,21-henicosanediol, chimyl alcohol, batyl alcohol, selachyl alcohol, and dimeric acid diol.

16. The optical waveguide of claim 2 , wherein said cured composition has a cured modulus of elasticity of from about 0.5 to 3.0 MPa at room temperature (20° C.) and 50% relative humidity.

17. The optical waveguide of claim 16 , wherein said cured composition has a cured modulus of elasticity of from about 1.0 to 2.5 MPa at room temperature (20° C.) and 50% relative humidity.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 1, 2007
From: ALCATEL-LUCENT (FORMERLY KNOWN AS ALCATEL)
To: DRAKA COMTEQ B.V.
Reel/Frame 019899/0132 →