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US4571349A
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Crosslinkable organopolysiloxanes and a method for preparing the same
Assignee: Wacker Chemie AG
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Filing: 1984-12-28
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Granted: 1986-02-18
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Expires: 2004-12-28
Abstract
Abstract Organopolysiloxanes which are crosslinked by high energy radiation consisting essentially of siloxane units of the formulas: (a) HR 1 C═CR 2 COOR 3 SiR 2 O 1/2 , (b) HSR 4 SiRO and (c) R 2 5 SiO where R is a monovalent hydrocarbon radical or a halogenated monovalent hydrocarbon radical, R 1 is hydrogen or a phenyl radical or a halogenated phenyl radical, R 2 is hydrogen or an alkyl radical having from 1 to 4 carbon atoms per radical and R 3 is a hydrocarbon radical or a halogenated hydrocarbon radical, R 4 is a divalent hydrocarbon radical, R 5 is the same as R or a hydrocarbon radical substituted with the HR 1 C═CR 2 COO group, where R 1 and R 2 are the same as above, in which two siloxane units of the formula HR.sup.1 C═CR.sup.2 COOR.sup.3 SiR.sub.2 O.sub.1/2 are present per molecule. These organopolysiloxanes are prepared by equilibrating the corresponding siloxanes in accordance with the conventional methods known in the art. These organopolysiloxanes can be crosslinked by high energy radiation, for example, ultraviolet radiation, to form coatings on paper for releasing tacky substances or as coatings on optic fibers and as photocuring sealants for electronic components.
Inventors
- 👤 Friedrich Hockemeyer
- 👤 Peter John
- 👤 Johann Muller
- 👤 Gerhard Preiner
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-11-02 12:09
CPC Classifications
D; D21; D21H; D21H27/00; D21H27/001; C; C08; C08G; C08G77/00; C08G77/04; C08G77/20; C08G77/22; C08G77/28; C09; C09D; C09D183/00; C09D183/04; C09D183/08
Claims Analysis
Total Claims: 10
Claim 1
Independent Claim
206 words
Organopolysiloxanes in which at least 95 mol percent of the siloxane units consist of units of the formulas: (a) HR 1 C═CR 2 COOR 3 SiR 2 O 1/2 (b) HSR 4 SiRO and (c) R 2 5 SiO where R is selected from the group consisting of a monovalent hydrocarbon radical and a halogenated monovalent hydrocarbon radical, R 1 is selected from the group consisting of hydrogen, a phenyl radical and a halogenated phenyl radical, R 2 is selected from the group consisting of hydrogen and an alkyl radical containing from 1 to 4 carbon atoms per radical, R 3 is selected from the group consisting of a divalent hydrocarbon radical and a halogenated divalent hydrocarbon radical, R 4 is a divalent hydrocarbon radical, R 5 is selected from the group consisting of R and a hydrocarbon radical substituted with the HR 1 C═CR 2 COO group, where R 1 and R 2 are the same as above, in which two siloxane units of the formula HR 1 C═CR 2 COOR 3 SiR 2 O 1/2 are present per molecule and at least 95 percent of the Si-bonded oxygen atoms present in the siloxane units having the HS group are present in the .tbd.SiOSi.tbd. grouping.
Claim 2
Dependent Claim
206 words
Organopolysiloxanes in which at least 95 mol percent of the siloxane units consist of units of the formulas: (a) HR 1 C═CR 2 COOR 3 SiR 2 O 1/2 (b) HSR 4 SiRO and (c) R 2 5 SiO where R is selected from the group consisting of a monovalent hydrocarbon radical and a halogenated monovalent hydrocarbon radical, R 1 is selected from the group consisting of hydrogen, a phenyl radical and a halogenated phenyl radical, R 2 is selected from the group consisting of hydrogen and an alkyl radical containing from 1 to 4 carbon atoms per radical, R 3 is selected from the group consisting of a divalent hydrocarbon radical and a halogenated divalent hydrocarbon radical, R 4 is a divalent hydrocarbon radical, R 5 is selected from the group consisting of R and a hydrocarbon radical substituted with the HR 1 C═CR 2 COO group, where R 1 and R 2 are the same as above, in which two siloxane units of the formula HR 1 C═CR 2 COOR 3 SiR 2 O 1/2 are present per molecule and at least 95 percent of the Si-bonded oxygen atoms present in the siloxane units having the HS group are present in the .tbd.SiOSi.tbd. grouping.
Claim 3
Dependent Claim
146 words
The organopolysiloxanes of claim 1, wherein the organopolysiloxanes have the formula H.sub.2 C═CHCOO(CH.sub.2).sub.p SiR.sub.2 O{SiR[(CH.sub.2).sub.3 SH]O}.sub.m (SiR.sub.2.sup.5 O).sub.n SiR.sub.2 (CH.sub.2).sub.p OOCHC═CH.sub.2 in which R is selected from the group consisting of a monovalent hydrocarbon radical and a halogenated monovalent hydrocarbon radical, R 5 is selected from the group consisting of R and a hydrocarbon radical substituted with the HR 1 C═CR 2 COO group, where R 1 is selected from the group consisting of hydrogen, a phenyl radical and a halogenated phenyl radical R 2 is selected from the group consisting of hydrogen and an alkyl radical containing from 1 to 4 carbon atoms per radical, m is a whole number having a value of from 1 to 30, n is a whole number having a value of from 10 to 1000 and p is a whole number having a value of from 1 to 6.
Claim 4
Dependent Claim
34 words
A method for coating a substrate which comprises applying the organopolysiloxanes of claim 1 to a substrate and thereafter exposing the coated substrate to high energy radiation to form an abrasion resistant coating thereon.
Claim 5
Dependent Claim
34 words
A method for coating a substrate which comprises applying the organopolysiloxanes of claim 2 to the substrate and thereafter exposing the coated substrate to high energy radiation to form an abrasion resistant coating thereon.
Claim 6
Dependent Claim
10 words
The method of claim 3 wherein the substrate is paper.
Claim 7
Dependent Claim
10 words
The method of claim 4, wherein the substrate is paper.
Claim 8
Dependent Claim
10 words
The coated substrate obtained from the method of claim 3.
Claim 9
Dependent Claim
262 words
A method for preparing the organopolysiloxanes of claim 2, which comprises equilibrating an organo(poly)siloxane having the formula: CH.sub.2 ═CHCOO(CH.sub.2).sub.p SiR.sub.2 O(SiR.sub.2.sup.5 O).sub.x SiR.sub.2 (CH.sub.2).sub.p OOCHC═CH.sub.2 in which R is selected from the group consisting of a monovalent hydrocarbon radical and a halogenated monovalent hydrocarbon radical, R 5 is selected from the group consisting of R and a hydrocarbon radical substituted with the HR 1 C═CR 2 COO group, R 1 is selected from the group consisting of hydrogen, a phenyl radical and a halogenated phenyl radical, R 2 is selected from the group consisting of hydrogen and an alkyl radical containing from 1 to 4 carbon atoms per radical, p is a whole number having a value of from 1 to 6 and x is 0 or a whole number having a value of from 1 to 1000 with a siloxane selected from the group consisting of (i) a linear organo(poly)siloxane having the formula: HO{SiR[(CH.sub.2).sub.3 SH]O}.sub.m (R.sub.2.sup.5 O).sub.x H, (ii) a cyclic organopolysiloxane having units of the formula SiR[(CH 2 ) 3 SH]O and mixtures thereof with the priviso that the cyclic organopolysiloxane may contain units of the formula SiR.sub.2.sup.5 O, in which the total number of siloxane units in such a cyclic organopolysiloxane is from 3 to 6 per molecule, in which R and R 5 are the same as above, m is a whole number having a value of from 1 to 30, and x is the same as above in the presence of an acid catalyst and at a temperature of from about 70° C. to about 150° C.
Claim 10
Dependent Claim
132 words
The process of claim 8, wherein a siloxane selected from the group consisting of a linear organo(poly)siloxane having the formula HO(SiR.sub.2.sup.5 O).sub.n H, a cyclic organo(poly)siloxane of the formula (SiR.sub.2.sup.5 O).sub.q and mixtures thereof is present in the equilibration reaction, wherein R 5 is selected from the group consisting of R and a hydrocarbon radical substituted with the HR 1 C═CR 2 COO group, R 1 is selected from the group consisting of hydrogen, a phenyl radical and a halogenated phenyl radical, R 2 is selected from the group consisting of hydrogen and an alkyl radical containing from 1 to 4 carbon atoms per radical, n is a whole number having a value of from 10 to 1000 and q is a whole number having a value of from 3 to 6.
References Cited (Backward Citations)
US4290869A
Cited
US4359369A
Cited
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