Claims
- 1. A flame-resistant silicone composition curable by UV irradiation to an elastomer comprising:(a) a reactive silicone resin component comprising a reactive polyorganosiloxane having at least one carboxylate-containing functional group (b) optionally, an inorganic filler component; (c) a photoinitiator component; and (d) a flame-retardant component in an amount effective to enhance the resistance of said composition to flammability, wherein the flame-retardant component is the combination of hydrated alumina and a member selected from the group consisting of organo ligand complexes of transition metals, organosiloxane ligand complexes of transition metals, and combinations thereof.
- 2. The composition according to claim 1, further comprising a triazole component.
- 3. The composition according to claim 1, further comprising a reactive diluent component.
- 4. The composition according to claim 1, wherein the reactive silicone resin is within the formula: wherein R1, R2 and R3 may be the same or different and are organo groups selected from the group consisting of alkyl, halo alkyls, substituted or unsubstituted aryl, vinyl, methacryloxypropyl, mercaptopropyl, hydrogen and benzoin; R4 is H or C1-5 alkyl; R5 is C1-8 alkylene; and n is at least 80.
- 5. The composition according to claim 1, wherein the inorganic filler component is a fumed hydrophobic silica filler.
- 6. The composition according to claim 5, wherein the fumed silica filler is a member selected from the group consisting of dimethyldichlorosilane-treated silica, hexamethyldisilazane-treated silica, and combinations thereof.
- 7. The composition according to claim 5, wherein the fumed silica filler is present at a level in range of about 4 to about 10 weight percent.
- 8. The composition according to claim 1, wherein the flame-retardant component is an organometallic one selected from the group consisting of organo ligand complexes of transition metals, organosiloxane ligand complexes of transition metals, and combinations thereof.
- 9. The composition according to claim 1, wherein the transition metals are selected from the group consisting of platinum, ruthenium, rhodium, and palladium. ligand complexes of transition metals, and combinations thereof.
- 10. The composition according to claim 2, wherein the triazole component is a member selected from the group consisting of benzotriazole and derivatives thereof.
- 11. The composition according to claim 3, wherein the reactive diluent is (meth)acrylate-terminated-dimethoxypropyldimethyl siloxane.
- 12. Reaction products of the composition according to claim 1.
- 13. A process for preparing a composition in accordance with claim 1, the steps of which comprise:providing and mixing together (a) a reactive silicone resin component comprising a reactive polyorganosiloxane having at least one carboxylate-containing functional group; (b) an inorganic filler component; (c) a photoinitiator component; and (d) a flame-retardant component in an amount effective to enhance the resistance of said composition to flammability.
- 14. A process for curing a composition in accordance with claim 1, the steps of which comprise:exposing the composition to radiation in the UV region of the electromagnetic spectrum for a time sufficient to effect cure.
- 15. The composition according to claim 1, wherein the carbroxylate containing functional group is a member selected from the group consisting of (meth)acrylate, maleate, cinnamate and combinations thereof.
- 16. The composition according to claim 14, wherein the carboxylate-containing functional group selected from the group consisting of (meth)acrylate, maleate, cinnamate and combinations thereof.
Parent Case Info
This is a continuation of provisional application 60/087,449 filed Jun. 1, 1998 and provisional application No. 60/119,953 filed Feb. 12, 1999.
PCT Information
Filing Document |
Filing Date |
Country |
Kind |
102e Date |
371c Date |
PCT/US99/11837 |
|
WO |
00 |
11/20/2000 |
11/20/2000 |
Publishing Document |
Publishing Date |
Country |
Kind |
WO99/62960 |
12/9/1999 |
WO |
A |
US Referenced Citations (17)
Foreign Referenced Citations (7)
Number |
Date |
Country |
1144237 |
Mar 1997 |
CN |
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EP |
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EP |
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Apr 1998 |
EP |
1323869 |
Jul 1973 |
GB |
2066277 |
Jul 1981 |
GB |
2039287 |
Aug 1989 |
GB |
Provisional Applications (2)
|
Number |
Date |
Country |
|
60/119953 |
Feb 1999 |
US |
|
60/087449 |
Jun 1998 |
US |