Ultraviolet radiation-curable silicone controlled release compositions

Claim 2

An ultraviolet radiation-curable controlled release composition comprising: (A) an epoxyfunctional diorganopolysiloxane comprising units of the formula RR'SiO, wherein R is hydrogen or C.sub.(1-8) alkyl and R' is R or a monovalent epoxyfunctional organic radical of from 2 to 20 carbon atoms, said diorganopolysiloxane having up to about 20% by weight epoxyfunctional groups and a viscosity of from about 50 centipoise to 200,000 centipoise at 25° C.; (B) a catalytic amount of a photocatalyst or a combination of photocatalysts; and (C) a small amount of epoxy monomer having two or more epoxy groups or a combination of epoxy monomers having two or more epoxy groups effective to raise the release of the cured controlled release composition.

Claim 3

A controlled release composition as defined in claim 1, wherein the photocatalyst component (B) is an onium salt having the formula: R.sub.2 I.sup.+ MX.sub.n.sup.-, R.sub.3 S.sup.+ MX.sub.n.sup.-, R.sub.3 Se.sup.+ MX.sub.n.sup.-, R.sub.4 P.sup.+ MX.sub.n.sup.-, or R.sub.4 N.sup.+ MX.sub.n.sup.- wherein radicals represented by R can be the same or different organic radicals of from 1 to 30 carbon atoms selected from the group comprising aromatic carbocyclic radicals of from 6 to 20 carbon atoms; aromatic carbocyclic radicals of from 6 to 20 carbon atoms substituted with from 1 to 4 monovalent organic radicals selected from C.sub.(1-8) alkoxy, C.sub.(1-8) alkyl, nitrogen, chloro, bromo, cyano, carboxy, mercapto; aromatic heterocyclic radicals selected from the group comprising pyridyl, thiophenyl, pyranyl; and wherein MX n - is a non-basic, non-nucleophilic anion selected from the group comprising BF 4 - , PF 6 - , AsF 6 - , SbF 6 - , SbCl 6 - , HSO 4 - , and ClO 4 - .

Claim 4

A controlled release composition as defined in claim 2, wherein the onium salt is a diaryl iodonium salt.

Claim 5

A controlled release composition as defined in claim 3, wherein said iodonium salt is selected from the group consisting of bis(dodecylphenyl)iodonium hexafluoroantimonate and bis(dodecylphenyl)iodonium hexafluoroarsenate.

Claim 6

A controlled release composition as defined in claim 3, further comprising as component (D), a small amount of monofunctional epoxy monomers sufficient to enhance the cure performance and promote anchorage of said controlled release compostitions.

Claim 7

A controlled release composition as defined in claim 3, wherein component (C) is selected from the group consisting of limonenedioxide, vinylcyclohexenedioxide, bis(2,3-epoxycyclopentyl ether, 3,4-epoxycyclohexylmethyl-3,4-epoxycyclohexanecarboxylate and butanedioldiglycidyl ether.

Claim 8

A controlled release coating composition as defined in claim 3, wherein component (C) is selected from limonenedioxide and vinylcyclohexenedioxide.

Claim 9

A controlled release composition as defined in claim 5, wherein component (C) is selected from limonenedioxide and vinylcyclohexenedioxide.

Claim 10

A controlled release composition as defined in claim 8, wherein the monofunctional epoxy monomer component (D) is a ω-epoxy C.sub.(8-11) aliphatic hydrocarbon.

Claim 11

A solid substrate coated on at lease one surface with a controlled release composition comprising: (A) an epoxyfunctional diorganopolysiloxane comprising units of the formula RR'SiO, wherein R is hydrogen or C.sub.(1-8) alkyl and R' is R or a monovalent epoxyfunctional organic radical of from 2 to 20 carbon atoms, said diorganopolysiloxane having up to about 20% by weight epoxyfunctional groups and a viscosity of from about 50 centipoise to 200,000 centipoise at 25° C.; (B) a catalytic amount of a photocatalyst or a combination of photocatalysts; and (C) a small amount of epoxy monomer having two or more epoxy groups or a combination of epoxy monomers having two or more epoxy groups effective to raise the release of the cured controlled release composition.

Claim 12

A solid substrate coated on at lease one surface with a controlled release composition comprising: (A) an epoxyfunctional diorganopolysiloxane comprising units of the formula RR'SiO, wherein R is hydrogen or C.sub.(1-8) alkyl and R' is R or a monovalent epoxyfunctional organic radical of from 2 to 20 carbon atoms, said diorganopolysiloxane having up to about 20% by weight epoxyfunctional groups and a viscosity of from about 50 centipoise to 200,000 centipoise at 25° C.; (B) a catalytic amount of a photocatalyst or a combination of photocatalysts; and (C) a small amount of epoxy monomer having two or more epoxy groups or a combination of epoxy monomers having two or more epoxy groups effective to raise the release of the cured controlled release composition.

Claim 13

A coated substrate as defined in claim 10, wherein said substrate is selected from the group consisting of paper, metal, foil, glass, polyethylene coated kraft paper, super calandered kraft paper, polyethylene films, polypropylene films and polyester films.

Claim 14

A coated substrate as defined in claim 10, wherein said controlled release composition has been cured on said substrate.

Claim 15

A process for preparing an ultraviolet radiation-curable epoxyfunctional silicone controlled release coating composition comprising: (1) reacting a vinyl-functional epoxide with a hydrogen-functional polysiloxane fluid in the presence of a catalytic amount of a hydrosilation catalyst; (2) recovering an epoxyfunctional polysiloxane reaction product; (3) adding a catalytic amount of photocatalyst; and (4) adding a small amount of epoxy monomer having two or more epoxy groups or a combination of epoxy monomers having two or more epoxy groups effective to raise the release of the cured controlled release composition.

Claim 16

A process for preparing an ultraviolet radiation-curable epoxyfunctional silicone controlled release coating composition comprising: (1) reacting a vinyl-functional epoxide with a hydrogen-functional polysiloxane fluid in the presence of a catalytic amount of a hydrosilation catalyst; (2) recovering an epoxyfunctional polysiloxane reaction product; (3) adding a catalytic amount of photocatalyst; and (4) adding a small amount of epoxy monomer having two or more epoxy groups or a combination of epoxy monomers having two or more epoxy groups effective to raise the release of the cured controlled release composition.

Claim 17

The process of claim 13, wherein said vinyl-functional epoxide is selected from the group consisting of limoneneoxide, 2,6-dimethyl-2,3-epoxy-7-octene, vinylcyclohexeneoxide, and 1,4-dimethyl-4-vinylcyclohexeneoxide; said photocatalyst is a diaryl iodonium salt; and said polyfunctional epoxy monomer is selected from vinylcyclohexenedioxide and limonenedioxide.

Claim 18

The process of claim 14, further comprising the additional step (5) of adding a small amount of monofunctional epoxy monomer sufficient to enhance cure and anchorage of said controlled release composition.

Claim 19

The process of claim 14, wherein the vinyl-functional epoxide is limoneneoxide, the hydrogen-functional polysiloxane fluid is a polydimethyl-methylhydrogen siloxane copolymer, the photocatalyst is a bis(dodecylphenyl)iodonium hexafluoroantimonate, and the polyfunctional epoxy monomer is limonenedioxide.

Claim 20

The process of claim 15, wherein the vinyl-functional epoxide is limoneneoxide, the hydrogen-functional polysiloxane fluid is a polydimethyl-methylhydrogen siloxane copolymer, the photocatalyst is a bis(dodecylphenyl)iodonium hexafluoroantimonate, the polyfunctional epoxy monomer is limonenedioxide, and the monofunctional epoxy monomer is a ω-epoxy C.sub.(8-11) aliphatic hydrocarbon.