IP Library Granted Patent US 8,724,956
Granted Patent B2
US 8,724,956 · App. 13/797,935 · Granted May 13, 2014

D1451 radiation curable supercoatings for multi-mode optical fiber

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Quick Facts
Patent No.
US 8,724,956
App. No.
13/797,935
Granted
May 13, 2014
Kind
B2
Abstract

The first aspect of the instant claimed invention is a method of formulating radiation curable Supercoatings for application to an optical fiber used in a telecommunications network. A Multi-layer Film Drawdown Method useful in the Method of formulating radiation curable Supercoatings is also described and claimed. Single mode Optical fibers coated with specific radiation curable Supercoatings are also described and claimed.

Claims (80)

1. A method of making a multi-mode optical fiber that has a primary coating layer that is in contact with the outer surface of the optical fiber and a secondary coating layer that is in contact with the outer surface of the primary coating layer, the method comprising the steps of:

forming the primary coating layer by curing a composition comprising:

55.91 wt. % of an oligomer prepared by reaction of:

3.38 wt. % of 2,4-toluene diisocyanate,

0.05 wt. % of 2,6-di-tert-butyl-p-cresol,

0.01 wt. % of acrylic acid,

1.46 wt. % of 2-hydroxyethyl acrylate,

50.10 wt. % of polypropylene glycol, MW=4200, and

0.03 wt. % of dibutyltin dilaurate;

40.29 wt. % ethoxylated nonyl phenol acrylate;

1.50 wt. % of bisphenol A ethoxylate diacrylate;

1.70 wt. % of 2,4,6-trimethylbenzoyldiphenylphosphine oxide type photoinitiator;

0.50 wt. % of hindered phenol antioxidant;

0.10 wt. % of bis(1-octyloxy-2,2,6,6-tetramethyl-4-piperidyl)sebacate; and

0.90 wt. % of γ-mercaptopropyltrimethoxysilane; and

forming the secondary coating layer by curing a composition selected from the group of formula compositions (a), (b), (c) and (d) that are defined as follows:

(a) 28.78 wt. % of an oligomer prepared by reaction of:

21.26 wt. %, by weight of the oligomer, of an 80/20 blend of the 2,4- and 2,6-isomer of toluene diisocyanate,

0.05 wt. %, by weight of the oligomer, of 2,6-di-tert-butyl-4-methylphenol,

14.18 wt. %, by weight of the oligomer, of 2-hydroxyethyl acrylate,

0.05 wt. %, by weight of the oligomer, of dibutyltin dilaurate, and

64.46 wt. %, by weight of the oligomer, of polypropylene glycol, MW=1000;

38.42 wt. % of difunctional bisphenol A-based epoxy acrylate oligomer;

7.2 wt. % of isobornyl acrylate;

8.15 wt. % of 2-phenoxyethyl acrylate;

5.76 wt. % of tripropylene glycol diacrylate;

4.27 wt. % of 1,6-hexanediol diacrylate;

2.43 wt. % of a blend, wherein said blend consists essentially of 35 wt. % of aromatic acid acrylate half ester and 65 wt. % of ethoxylated trimethylolpropane triacrylate;

1 wt. % of 2,4,6-trimethylbenzoyldiphenylphosphine oxide type photoinitiator;

3 wt. % of 1-hydroxycyclohexyl-phenyl ketone;

0.5 wt. % of hindered phenol antioxidant;

0.33 wt. % of a blend, wherein said blend consists essentially of, 40 to 70 wt. % of dimethyl, methyl(propyl(poly(ethylene oxide) (propylene oxide))acetate)siloxane, 30 to 60 wt. % of poly(ethylene oxide propylene oxide) monoallyl ether acetate, and less than 9 wt. % of polyether polyol acetate; and

0.17 wt. % of dimethyl, methyl(propyl(poly(ethylene oxide))acetate) siloxane;

(b) 30.00 wt. % of an oligomer prepared by reaction of 21.26 wt. %, by weight of the oligomer, of an 80/20 blend of the 2,4- and 2,6- isomer of toluene diisocyanate,

0.05 wt. %, by weight of the oligomer, of 2,6-di-tert-butyl-4-methylphenol,

14.18 wt. %, by weight of the oligomer, of 2-hydroxyethyl acrylate,

0.05 wt. %, by weight of the oligomer, of dibutyltin dilaurate, and

64.46 wt. %, by weight of the oligomer, of polypropylene glycol, MW=1000;

40.00 wt. % of epoxy diacrylate;

7.5 wt. % of isobornyl acrylate;

8.5 wt. % of 2-phenoxyethyl acrylate;

6 wt. % of tripropylene glycol diacrylate;

4.5 wt. % of 1,6-hexanediol diacrylate;

0.5 wt. % of hindered phenol antioxidant;

0.5 wt. % of 2,4,6-trimethylbenzoyldiphenylphosphine oxide type photoinitiator;

2 wt. % of 1-hydroxycyclohexyl-phenyl ketone;

0.33 wt. % of a blend, wherein said blend consists essentially of, 40 to 70 wt. % of dimethyl, methyl(propyl(poly(ethylene oxide) (propylene oxide))acetate)siloxane, 30 to 60 wt. % of poly(ethylene oxide propylene oxide) monoallyl ether acetate, and less than 9 wt. % of polyether polyol acetate; and

0.17 wt. % of dimethyl, methyl(propyl(poly(ethylene oxide))acetate) siloxane;

(c) 20.27 wt. % of an oligomer prepared by reaction of:

21.26 wt. %, by weight of the oligomer, of an 80/20 blend of the 2,4- and 2,6-isomer of toluene diisocyanate,

0.05 wt. %, by weight of the oligomer, of 2,6-di-tert-butyl-4-methylphenol,

14.18 wt. %, by weight of the oligomer, of 2-hydroxyethyl acrylate,

0.05 wt. %, by weight of the oligomer, of dibutyltin dilaurate, and

64.46 wt. %, by weight of the oligomer, of polypropylene glycol, MW=1000;

50.00 wt. % of epoxy diacrylate;

1.06 wt. % of 2,4,6-trimethylbenzoyldiphenylphosphine oxide type photoinitiator;

0.80 wt. % of 1-hydroxycyclohexyl phenyl ketone;

0.50 wt. % of 2,6-di-tert-butyl-4-methylphenol;

1.06 wt. % of a blend, wherein said blend consists essentially of, 70 wt. % of oligo[2-hydroxy-2-methyl- 1-[4(1-methyl-vinyl)phenyl]propanone] and 30 wt. % of 2- hydroxy- 2- methyl- 1-phenylpropanone;

15.00 wt. % of tripropylene glycol diacrylate;

9.80 wt. % of 1,6-hexanediol diacrylate;

0.50 wt. % of ethoxylated(4) nonyl phenol acrylate, MW=450;

0.68 wt. % of a blend, wherein said blend consists essentially of, 40 to 70 wt. % of dimethyl, methyl(propyl(poly(ethylene oxide) (propylene oxide))acetate)siloxane,

30 to 60 wt. % of poly(ethylene oxide propylene oxide) monoallyl ether acetate, and less than 9 wt. % of polyether polyol acetate; and

0.33 wt. % of dimethyl, methyl(propyl(poly(ethylene oxide))acetate) siloxane; and

(d) 28.1 wt. % of an oligomer prepared by reaction of:

21.26 wt. %, by weight of the oligomer, of an 80/20 blend of the 2,4- and 2,6-isomer of toluene diisocyanate,

0.05 wt. %, by weight of the oligomer, of 2,6-di-tert-butyl-4-methylphenol,

14.18 wt. %, by weight of the oligomer, of 2-hydroxyethyl acrylate,

0.05 wt. %, by weight of the oligomer, of dibutyltin dilaurate, and

64.46 wt. %, by weight of the oligomer, of polypropylene glycol, MW=1000;

37.4 wt. % of a difunctional bisphenol A-based epoxy acrylate oligomer;

5.2 wt. % of 1,6-hexanediol diacrylate;

10.3 wt. % of ethoxylated 4 bisphenol A diacrylate;

14.75 wt. % of 2-phenoxyethyl acrylate;

0.75 wt. % of 2,4,6-trimethylbenzoyldiphenylphosphine oxide type photoinitiator;

2.5 wt. % of 1-hydroxcyclohexyl phenyl ketone;

0.5 wt. % of hindered phenol antioxidant;

0.33 wt. % of a blend of 40 to 70 wt. % of dimethyl, methyl(propyl(poly(ethylene oxide) (propylene oxide))acetate)siloxane, 30 to 60 wt. % of poly(ethylene oxide propylene oxide) monoallyl ether acetate, and less than 9 wt. % of polyether polyol acetate; and

0.17 wt. % of dimethyl, methyl(propyl(poly(ethylene oxide))acetate) siloxane.

Assignments (4)
CHANGE OF CORPORATE ADDRESS Recorded Mar 30, 2022
From: COVESTRO (NETHERLANDS) B.V.
To: COVESTRO (NETHERLANDS) B.V.
Reel/Frame 059546/0570 →
CHANGE OF NAME Recorded Jul 2, 2021
From: MS HOLDING B.V.
To: COVESTRO (NETHERLANDS) B.V.
Reel/Frame 056756/0513 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 25, 2021
From: DSM IP ASSETS B.V.
To: MS HOLDING B.V.
Reel/Frame 056726/0106 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 12, 2013
From: WU, XIAOSONG; SCHMID, STEVEN ROBERT; BISHOP, TIMOTHY EDWARD; ZIMMERMAN, JOHN MONROE; CATTRON, WENDELL WAYNE; MURPHY, EDWARD JOSEPH; SHAH, PRATIK
To: DSM IP ASSETS B.V.
Reel/Frame 030202/0957 →