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US4762887A
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Process for preparing acrylate-functional organopolysiloxane-urethane copolymers
Assignee: Wacker Chemical Corp
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Filing: 1987-01-15
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Granted: 1988-08-09
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Expires: 2007-01-15
Abstract
Abstract A process for preparing radiation polymerizable acrylate-functional organopolysiloxane-urethane copolymers by reacting aminofunctional polysiloxanes with acrylated urethane oligomers in the presence of a solvent.
Inventors
- 👤 Roy M. Griswold
- 👤 Douglas G. Vanderlaan
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-10-29 23:46
CPC Classifications
C; C08; C08L; C08L83/00; C08L83/10; C08G; C08G77/00; C08G77/42; C08G77/452; C08G77/455; C08L75/00; C08L75/04; C08L75/14; C08L75/16; Y; Y10; Y10S; Y10S525/00; Y10S525/92
Claims Analysis
Total Claims: 12
Claim 1
Independent Claim
329 words
A process for preparing radiation polymerizable acrylate-functional organopolysiloxane-urethane copolymers which comprises reacting an aminofunctional polysiloxane fluid having at least one unit of the formula ##STR13## where R is a divalent radical selected from the group consisting of a saturated divalent hydrocarbon radical having up to 20 carbon atoms, a divalent hydrocarbonoxy radical in which the oxygen atom is in the form of an ether linkage and an unsaturated divalent hydrocarbon radical having from 2 to 20 carbon atoms, R 1 is a monovalent hydrocarbon radical having from 1 to 20 carbon atoms, R 2 is a radical selected from the group consisting of a monovalent hydrocarbon radical having from 1 to 20 carbon atoms and a radical of the formula CH.sub.2 CH.sub.2 X, where X is selected from the group consisting of COOR 3 , CONR 3 , CN and SO 2 R 3 , R 3 is a monovalent hydrocarbon radical having from 1 to 20 carbon atoms, a is 0, 1 or 2, b is 1, 2 or 3, c is 1, 2, 3 or 4 and d is 0, 1, 2 or 3, with the proviso that c equals b-d+1 with an acrylated urethane oligomer in a mole ratio of acrylate groups to amine groups of from 0.75 to 10 in the presence of an organic solvent at a temperature of from 25° to 150° C., in which the acrylated urethane oligomer is obtained by reacting an organic compound having at least two active hydrogen groups with an excess of an organic polyisocyanate having at least two --NCO groups per molecule to form a urethane prepolymer having at least two --NCO groups per molecule and thereafter the --NCO containing prepolymer is reacted with a hydroxy-containing compound selected from the group consisting of an acrylic compound, a methacrylic compound, and an acrylamide compound in a mole ratio of --NCO group to OH group of from 0.5:1 to 1:0.5 at a temperature of from 25° to 150° C.
Claim 2
Dependent Claim
329 words
A process for preparing radiation polymerizable acrylate-functional organopolysiloxane-urethane copolymers which comprises reacting an aminofunctional polysiloxane fluid having at least one unit of the formula ##STR13## where R is a divalent radical selected from the group consisting of a saturated divalent hydrocarbon radical having up to 20 carbon atoms, a divalent hydrocarbonoxy radical in which the oxygen atom is in the form of an ether linkage and an unsaturated divalent hydrocarbon radical having from 2 to 20 carbon atoms, R 1 is a monovalent hydrocarbon radical having from 1 to 20 carbon atoms, R 2 is a radical selected from the group consisting of a monovalent hydrocarbon radical having from 1 to 20 carbon atoms and a radical of the formula CH.sub.2 CH.sub.2 X, where X is selected from the group consisting of COOR 3 , CONR 3 , CN and SO 2 R 3 , R 3 is a monovalent hydrocarbon radical having from 1 to 20 carbon atoms, a is 0, 1 or 2, b is 1, 2 or 3, c is 1, 2, 3 or 4 and d is 0, 1, 2 or 3, with the proviso that c equals b-d+1 with an acrylated urethane oligomer in a mole ratio of acrylate groups to amine groups of from 0.75 to 10 in the presence of an organic solvent at a temperature of from 25° to 150° C., in which the acrylated urethane oligomer is obtained by reacting an organic compound having at least two active hydrogen groups with an excess of an organic polyisocyanate having at least two --NCO groups per molecule to form a urethane prepolymer having at least two --NCO groups per molecule and thereafter the --NCO containing prepolymer is reacted with a hydroxy-containing compound selected from the group consisting of an acrylic compound, a methacrylic compound, and an acrylamide compound in a mole ratio of --NCO group to OH group of from 0.5:1 to 1:0.5 at a temperature of from 25° to 150° C.
Claim 3
Dependent Claim
20 words
The process of claim 1, where the molar ratio of acrylate groups to amine groups ranges from 1 to 5.
Claim 4
Dependent Claim
25 words
The process of claim 1, wherein the organic solvent is selected from the group consisting of aliphatic hydrocarbons, aromatic hydrocarbons, alcohols, ethers and halogenated hydrocarbons.
Claim 5
Dependent Claim
14 words
Radiation polymerizable acrylate-functional organopolysiloxane-urethane copolymers prepared in accordance with the process of claim 1.
Claim 6
Dependent Claim
16 words
A radiation polymerizable composition containing the acrylate-functional organopolysiloxaneurethane copolymers prepared in claim 1 and a photosensitizer.
Claim 7
Dependent Claim
27 words
The composition of claim 5, wherein the photosensitizer is present in an amount up to 15 weight percent, based on the weight of the acrylate-functional organopolysiloxane-urethane copolymers.
Claim 8
Dependent Claim
31 words
The composition of claim 5, wherein the photosensitizer is present in an amount of from about 0.5 to about 10 weight percent, based on the weight of the acrylate-functional organopolysiloxane-urethane copolymers
Claim 9
Dependent Claim
64 words
The composition of claim 5, wherein the composition contains from 0.001 to about 99 weight percent based on the weight of the acrylate-functional organopolysiloxane-urethane copolymers of a reactive diluent selected from the group consisting of ethyl acrylate, n-amyl acrylate, benzyl acrylate, cyclohexyl acrylate, 2-(N-methylcarbamoyloxy)ethylacrylate, diethylaminoethyl acrylate, 2-ethoxyethyl acrylate, lauryl acrylate, n-octyl acrylate, octadecyl acrylate and the correspnding methacrylate esters, vinyl acetate and N-vinyl pyrrolidone.
Claim 10
Dependent Claim
17 words
A heat polymerizable composition containing the acrylate-functional organopolysiloxane-urethane copolymers prepared in claim 1 and an organic peroxide.
Claim 11
Dependent Claim
30 words
The composition of claim 9, wherein the organic peroxide is present in an amount of from 0.1 to 10 weight percent based on the weight of the acrylate-functional organopolysiloxane-urethane copolymers.
Claim 12
Dependent Claim
64 words
The composition of claim 9, wherein the composition contains from 0.001 to about 99 weight percent based on the weight of the acrylate-functional organopolysiloxane-urethane copolymers of a reactive diluent selected from the group consisting of ethyl acrylate, n-amyl acrylate, benzyl acrylate, cyclohexyl acrylate, 2-(N-methylcarbamoyloxy)ethylacrylate, diethylaminoethyl acrylate, 2-ethoxyethyl acrylate, lauryl acrylate, n-octyl acrylate, octadecyl acrylate and the corresponding methacrylate esters, vinyl acetate and N-vinyl pyrrolidone.
References Cited (Backward Citations)
USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1991-08-09 | 1992-02-08 | 1992-08-09 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1995-08-09 | 1996-02-08 | 1996-08-09 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1999-08-09 | 2000-02-08 | 2000-08-09 | $7700.00 | Window Closed / Lapsed |