US5082686A
Expired / Lapsed
US
⏱️ 0.0 years remaining
UV curable non-toxic epoxysilicone release coating compositions and method
Assignee: General Electric Co
•
Filing: 1990-12-03
•
Granted: 1992-01-21
•
Expires: 2010-12-03
Abstract
Abstract There is provided a curable substantially uniform mixture of an epoxy silicone, polyarylonium salts and a compatibilizer in the form a mixture of a long chain alkyl substituted phenol and an alkane diol. The curable mixture is convertable to a non-toxic, tack free adherent release coating for pressure sensitive adhesives.
Inventors
- 👤 James L. Desorcie
- 👤 Michael J. O'Brien
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-11-09 04:43
CPC Classifications
C; C08; C08G; C08G59/00; C08G59/18; C08G59/20; C08G59/22; C08G59/30; C08G59/306; C08G59/68
Claims Analysis
Total Claims: 8
Claim 1
Independent Claim
190 words
A method for providing nontoxic, adherent silicone release coatings which can be used in food applications comprising: (1) applying a UV curable silicone coating onto a substrate, and (2) exposing the treated substrate of (1) to UV radiation until the UV curable silicone coating is tack-free, where the UV curable epoxy silicone composition comprises by weight (A) 100 parts of epoxysilicone having from 5 to 12 mole percent epoxysiloxy units, based on the total moles of condensed diorganosiloxy units in the epoxysilicone, (B) 1 to 25 parts of a compatibilizer in the form of a mixture of (i) 1 to 25 parts of a C.sub.(8-20) alkylphenol and (ii) 0 to 15 parts of a C.sub.(4-12) alkanediol, and (C) an effective amount of a polyarylonium hexafluorometal, or metalloid salt, substituted with at least one nuclear bound alkoxy radical having at least 8 carbon atoms selected from the class consisting of diaryliodonium salts and triarylsulfonium salts and the UV curable epoxy silicone composition is a mixture prepared by initially forming a solution of the arylonium salt in the alkylphenol and alkane diol and thereafter blending the resulting solution into the epoxy silicone.
Claim 2
Independent Claim
190 words
A method for providing nontoxic, adherent silicone release coatings which can be used in food applications comprising: (1) applying a UV curable silicone coating onto a substrate, and (2) exposing the treated substrate of (1) to UV radiation until the UV curable silicone coating is tack-free, where the UV curable epoxy silicone composition comprises by weight (A) 100 parts of epoxysilicone having from 5 to 12 mole percent epoxysiloxy units, based on the total moles of condensed diorganosiloxy units in the epoxysilicone, (B) 1 to 25 parts of a compatibilizer in the form of a mixture of (i) 1 to 25 parts of a C.sub.(8-20) alkylphenol and (ii) 0 to 15 parts of a C.sub.(4-12) alkanediol, and (C) an effective amount of a polyarylonium hexafluorometal, or metalloid salt, substituted with at least one nuclear bound alkoxy radical having at least 8 carbon atoms selected from the class consisting of diaryliodonium salts and triarylsulfonium salts and the UV curable epoxy silicone composition is a mixture prepared by initially forming a solution of the arylonium salt in the alkylphenol and alkane diol and thereafter blending the resulting solution into the epoxy silicone.
Claim 3
Dependent Claim
15 words
A method in accordance with claim 1, where the substrate is a super calendered kraft.
Claim 4
Dependent Claim
14 words
A method in accordance with claim 1, where the substrate is a polyethylene kraft.
Claim 5
Dependent Claim
15 words
A method in accordance with claim 1, where the polyarylonium salt is a diphenyliodonium salt.
Claim 6
Dependent Claim
14 words
A method in accordance with claim 4, where the diphenyliodonium salt is (4-octyloxyphenyl)phenyliodonium hexafluoroantimonate.
Claim 7
Dependent Claim
15 words
A method in accordance with claim 1 where the polyarylonium salt is a triarylsulfonium salt.
Claim 8
Dependent Claim
14 words
A method in accordance with claim 6, where the triarylsulfonium salt is bis(4-dodecyloxyphenyl)phenylsulfonium hexafluoroantimonate.
References Cited (Backward Citations)
US3726710A
Cited
US4173551A
Cited
US4113939A
Cited
US4201808A
Cited
US4279717A
Cited
US4348454A
Cited
US4576999A
Cited
US4816496A
Cited
EP0334056A2
Cited
US4882201A
Cited
EP0355381A1
Cited
US4954364A
Cited
US4994299A
Cited
USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1995-01-20 | 1995-07-22 | 1996-01-21 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1999-01-20 | 1999-07-22 | 2000-01-21 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 2003-01-20 | 2003-07-22 | 2004-01-21 | $7700.00 | Window Closed / Lapsed |