US4690501A
Expired / Lapsed
US
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Ultraviolet curable optical glass fiber coatings from acrylate terminated, end-branched polyurethane polyurea oligomers
Assignee: DeSoto Inc
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Filing: 1985-07-08
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Granted: 1987-09-01
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Expires: 2005-07-08
Abstract
Abstract Ultraviolet curing oligomers and liquid coating compositions based thereon are disclosed which cure with ultraviolet light in the presence of a photoinitiator. The coating compositions can provide either a single coating for optical glass fiber which resists microbending difficulties down to around -40° C., or a topcoat for overcoating softer buffer coatings which resist microbending down to around -60° C. The coating compositions consist essentially of the linear polyacrylate-terminated polyurethane polyurea oligomer in admixture with an ultraviolet curable liquid acrylate or polyacrylate to provide the liquidity needed for application and to adjust the hardness or softness of the cured coating for the selected single coat or topcoat utility. The oligomer contains a linear polyurethane core terminated by urea formation with a polyhydroxy-functional amine containing a single isocyanate-reactive amino hydrogen atom. The plurality of hydroxy-terminated branches provided by the amine are capped with an acrylate-functional compound, and the several acrylate-functional branches increase the toughness and the cure speed.
Inventors
- 👤 John M. Zimmerman
- 👤 Gerry K. Noren
- 👤 Timothy E. Bishop
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-10-28 15:31
CPC Classifications
C; C08; C08G; C08G18/00; C08G18/06; C08G18/70; C08G18/81; C08G18/8141; C08G18/815; C08G18/8158; C08G18/8175; C03; C03C; C03C25/00; C03C25/10; C03C25/104; C03C25/106; C03C25/1065; C08F; C08F299/00; C08F299/02; C08F299/06; C08F299/065; C08G18/08; C08G18/10; C08G18/28; C08G18/40; C08G18/48; C08G18/50; C08G18/5021; C08G18/5024; C08G18/67; C08G18/671; C08G18/672; Y; Y10; Y10T; Y10T428/00; Y10T428/29; Y10T428/2913; Y10T428/2933; Y10T428/2938
Claims Analysis
Total Claims: 26
Claim 1
Independent Claim
166 words
An ultraviolet curing liquid coating composition which, when cured with ultraviolet light in the presence of a photoinitiator, either provides a single coating for optical glass fiber having adequate strength at room or expected elevated temperature, and a low tensile modulus which remains low to resist microbending difficulties down to around -40° C., or which can be used to overcoat softer buffer coatings which remain soft to resist microbending difficulties down to around -60° C., said coating composition consisting essentially of a linear polyacrylate-terminated polyurethane polyurea oligomer containing a linear polyurethane core terminated at both ends by urea formation with a polyhydroxy-functional amine containing a single isocyanate-reactive amino hydrogen atom, the plurality of hydroxy-terminated branches provided by said amine being capped with an acrylate-functional compound, and said polyacrylate-terminated oligomer being in admixture with an ultraviolet curable liquid acrylate or polyacrylate to provide the liquidity needed for application and to adjust the hardness or softness of the cured coating for the selected single coat or topcoat utility.
Claim 2
Dependent Claim
166 words
An ultraviolet curing liquid coating composition which, when cured with ultraviolet light in the presence of a photoinitiator, either provides a single coating for optical glass fiber having adequate strength at room or expected elevated temperature, and a low tensile modulus which remains low to resist microbending difficulties down to around -40° C., or which can be used to overcoat softer buffer coatings which remain soft to resist microbending difficulties down to around -60° C., said coating composition consisting essentially of a linear polyacrylate-terminated polyurethane polyurea oligomer containing a linear polyurethane core terminated at both ends by urea formation with a polyhydroxy-functional amine containing a single isocyanate-reactive amino hydrogen atom, the plurality of hydroxy-terminated branches provided by said amine being capped with an acrylate-functional compound, and said polyacrylate-terminated oligomer being in admixture with an ultraviolet curable liquid acrylate or polyacrylate to provide the liquidity needed for application and to adjust the hardness or softness of the cured coating for the selected single coat or topcoat utility.
Claim 3
Dependent Claim
29 words
A coating composition as recited in claim 1 in which said polyacrylate-terminated oligomer constitutes at least about 30% up to about 80% of the reactive components in the coating.
Claim 4
Dependent Claim
29 words
A coating composition as recited in claim 1 in which said polyacrylate-terminated oligomer constitutes at least about 40% up to about 70% of the reactive components in the coating.
Claim 5
Dependent Claim
39 words
A coating composition as recited in claim 1 adapted for topcoat application in which said ultraviolet curable liquid comprises an acrylate-functional monomer whose homopolymer has a glass transition temperature above about 55° C. in the absence of acrylic acid.
Claim 6
Dependent Claim
28 words
A coating composition as recited in claim 1 adapted for topcoat application in which said ultraviolet curable liquid comprises a polyacrylate having a molecular weight below about 600.
Claim 7
Dependent Claim
34 words
A coating composition as recited in claim 1 adapted for single coat application in which said ultraviolet curable liquid comprises an acrylate-functional monomer, whose homopolymer has a glass transition temperature less than 0° C.
Claim 8
Dependent Claim
34 words
A coating composition as recited in claim 1 adapted for single coat application in which said ultraviolet curable liquid comprises an acrylate-functional monomer whose homopolymer has a glass transition temperature less than -20° C.
Claim 9
Dependent Claim
55 words
A coating composition as recited in claim 1 adapted for single coat application in which said ultraviolet curable liquid is a liquid linear aliphatic diacrylate in which the two acrylate groups are separated by at least a chain of 6 carbon atoms or by a molecular weight of at least 400 up to about 4000.
Claim 10
Dependent Claim
25 words
A coating composition as recited in claim 8 in which said two acrylate groups are separated by a molecular weight of from 600 to 2500.
Claim 11
Dependent Claim
20 words
A coating composition as recited in claim 9 in which said two acrylate groups are separated by a polyoxybutylene structure.
Claim 12
Dependent Claim
28 words
A coating composition as recited in claim 8 in which said linear liquid diacrylate is a polyoxybutylene glycol diacrylate having a molecular weight of from 800 to 2000.
Claim 13
Dependent Claim
42 words
A coating composition as recited in claim 1 in which said polyacrylate-terminated polyurethane oligomer has a molecular weight of about 1000 to about 8000 with one linking group selected from urethane and urea groups for every 300 to 900 units of weight.
Claim 14
Dependent Claim
72 words
A coating composition as recited in claim 1 in which said polyacrylate-terminated polyurethane polyurea oligomer is formed using diisocyanate in which a linear aliphatic chain containing at least 6 carbon atoms separates the two isocyanate groups, and this diisocyanate is reacted with a polyether or polyester containing alkylene groups having from 1 to 6 carbon atoms and a molecular weight in the range of 500 to 4000, to form a polyurethane diisocyanate.
Claim 15
Dependent Claim
19 words
A coating composition as recited in claim 13 in which said diisocyanate is provided by dimer fatty acid diisocyanate.
Claim 16
Dependent Claim
19 words
A coating composition as recited in claim 14 in which said dimer fatty acid diisocyanate contains 36 carbon atoms.
Claim 17
Dependent Claim
33 words
A coating composition as recited in claim 14 in which said diisocyanate is reacted with a polyether which is a polyoxyalkylene glycol having a molecular weight in the range of 1000 to 3000.
Claim 18
Dependent Claim
19 words
A coating composition as recited in claim 16 in which said oxyalkylene glycol contains 3 or 4 carbon atoms.
Claim 19
Dependent Claim
16 words
A coating composition as recited in claim 1 in which said acrylate-functional compound is 2-hydroxyethyl acrylate.
Claim 20
Dependent Claim
41 words
A linear polyacrylate-terminated polyurethane polyurea oligomer containing a linear polyurethane core terminated by urea formation with a polyhydroxy-functional amine containing a single isocyanate-reactive amino hydrogen atom, the plurality of hydroxy-terminated branches provided by said amine being capped with an acrylate-functional compound.
Claim 21
Dependent Claim
41 words
A linear polyacrylate-terminated polyurethane polyurea oligomer containing a linear polyurethane core terminated by urea formation with a polyhydroxy-functional amine containing a single isocyanate-reactive amino hydrogen atom, the plurality of hydroxy-terminated branches provided by said amine being capped with an acrylate-functional compound.
Claim 22
Dependent Claim
41 words
An oligomer as recited in claim 19 in which said polyacrylate-terminated polyurethane oligomer has a molecular weight of about 1000 to about 8000 with one linking group selected from urethane and urea groups for every 300 to 900 units of weight.
Claim 23
Dependent Claim
16 words
An optical glass fiber single coated with an ultraviolet-cured coating of the composition of claim 6.
Claim 24
Dependent Claim
16 words
An optical glass fiber single coated with an ultraviolet-cured coating of the composition of claim 8.
Claim 25
Dependent Claim
15 words
An optical glass fiber topcoated with an ultraviolet-cured coating of the composition of claim 4.
Claim 26
Dependent Claim
15 words
An optical glass fiber topcoated with an ultraviolet-cured coating of the composition of claim 5.
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USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1990-08-31 | 1991-03-02 | 1991-09-01 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1994-08-31 | 1995-03-02 | 1995-09-01 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1998-08-31 | 1999-03-02 | 1999-09-01 | $7700.00 | Window Closed / Lapsed |