US5239035A
Expired / Lapsed
US
⏱️ 0.0 years remaining
Curable organosiloxane gel compositions
Assignee: Dow Silicones Corp
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Filing: 1992-04-09
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Granted: 1993-08-24
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Expires: 2012-04-09
Abstract
Abstract The amount of solvent-extractable materials present in organosiloxane gels cured by a platinum-catalyzed hydrosilylation reaction can be reduced without sacrificing other desirable properties the gels when the curable composition used to prepare the gel comprise a first polydiorganosiloxane with vinyl or other ethylenically unsaturated hydrocarbon radicals only at the terminal positions, a second polydiorganosiloxane with silicon bonded hydrogen atoms only at the terminal positions and a crosslinking reactant containing at least three alkenyl radicals or silicon-bonded hydrogen atoms per molecule. The number of silicon-bonded hydrogen atoms or alkenyl radicals in excess of 2 per molecule of crosslinking reactant constitute from 10 to 30 percent of these reactive groups present in the curable composition.
Inventors
- 👤 Myron T. Maxson
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-11-05 22:55
CPC Classifications
C; C08; C08L; C08L83/00; C08L83/04; C08K; C08K5/00; C08K5/04; C08K5/05; C08K5/09; C08K5/098; C08K5/56; C08L83/08; C08G; C08G77/00; C08G77/04; C08G77/12; C08G77/20; C08G77/22; C08G77/24
Claims Analysis
Total Claims: 7
Claim 1
Independent Claim
177 words
A liquid organosiloxane composition that cures to a gel by means of a platinum group metal catalyzed hydrosilylation reaction and comprises A. 100 parts of a liquid polyorganosiloxane containing two alkenyl radicals per molecule; B. from 20 to 100 parts of a liquid diorganohydrogensiloxy-terminated polydiorganosiloxane; C. at least one crosslinking reactant selected from the group consisting of liquid polyorganosiloxanes containing at least three silicon-bonded reactive groups per molecule, where said reactive groups are, in turn, selected from the group consisting of a hydrogen atom and alkenyl radicals and the total number of reactive groups in excess of two per molecule of said crosslinking reactant constitutes from 10 to 30 percent of the number of said reactive groups present in said composition and the molar ratio of silicon bonded hydrogen atoms to alkenyl radicals in said composition is from 0.85 to about 1.0; and D. an amount sufficient to promote curing of said composition of a hydrosilylation catalyst selected from the group consisting of metals from the platinum group of the periodic table and compounds of these metals.
Claim 2
Dependent Claim
177 words
A liquid organosiloxane composition that cures to a gel by means of a platinum group metal catalyzed hydrosilylation reaction and comprises A. 100 parts of a liquid polyorganosiloxane containing two alkenyl radicals per molecule; B. from 20 to 100 parts of a liquid diorganohydrogensiloxy-terminated polydiorganosiloxane; C. at least one crosslinking reactant selected from the group consisting of liquid polyorganosiloxanes containing at least three silicon-bonded reactive groups per molecule, where said reactive groups are, in turn, selected from the group consisting of a hydrogen atom and alkenyl radicals and the total number of reactive groups in excess of two per molecule of said crosslinking reactant constitutes from 10 to 30 percent of the number of said reactive groups present in said composition and the molar ratio of silicon bonded hydrogen atoms to alkenyl radicals in said composition is from 0.85 to about 1.0; and D. an amount sufficient to promote curing of said composition of a hydrosilylation catalyst selected from the group consisting of metals from the platinum group of the periodic table and compounds of these metals.
Claim 3
Dependent Claim
174 words
A composition according to claim 1 where said liquid polyorganosiloxane A is represented by the formula ##STR5## where R 1 , R 2 , R 3 , and R 4 are identical or different monovalent unsubstituted or substituted hydrocarbon radicals, R 5 represents an alkenyl radical, the sum of m and n represents a molecular weight equivalent to a viscosity of from 0.2 to 20 Pa.s at 25° C. and the value of m is from 0 to 10n; the diorganohydrogensiloxy-terminated polydiorganosiloxane is represented by the general formula ##STR6## where R 6 , R 7 , R 8 , R 9 , and R 10 represent identical or different monovalent unsubstituted or substituted hydrocarbon radicals, p is O or a positive integer, q is a positive integer and the average value of the sum of p and q is at least three; and the total number of reactive groups in excess of two per molecule said crosslinking reactant constitutes form 10 to 15 percent of the number of reactive groups present in said composition.
Claim 4
Dependent Claim
82 words
A composition according to claim 2 where the hydrocarbon radicals represented by R 1 , R 2 , R 3 , R 6 , R 7 , R 9 and R 10 are lower alkyl radicals; R 4 and R 8 are --CH 2 CH 2 R f where R f represents a perfluoroalkyl radical; R 5 represents vinyl; and said catalyst is a complex of chloroplatinic acid and a liquid vinyl-containing organosiloxane compound; and the composition contains a platinum catalyst inhibitor.
Claim 5
Dependent Claim
33 words
A composition according to claim 3 where said lower alkyl radicals are methyl, R f is trifluoromethyl and said crosslinking reactant is represented by the formula ##STR7## where Me represents a methyl radical.
Claim 6
Dependent Claim
22 words
A composition according to claim 4 where said catalyst is microencapsulated within at least one layer of a thermoplastic or thermosetting polymer.
Claim 7
Dependent Claim
45 words
A composition according to claim 4 where the ingredients of said composition are packaged in at least two containers prior to being blended to form said composition, and where said catalyst is located in a different container than the organosilicon compounds containing silicon-bonded hydrogen atoms.
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USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1996-08-23 | 1997-02-22 | 1997-08-24 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 2000-08-23 | 2001-02-22 | 2001-08-24 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 2004-08-23 | 2005-02-22 | 2005-08-24 | $7700.00 | Window Closed / Lapsed |