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US4310678A Expired / Lapsed US ⏱️ 0.0 years remaining

Liquid copolymeric organopolysiloxanes comprising SiO2 and method therefor

Assignee: Dow Silicones Corp
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Filing: 1980-12-02
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Granted: 1982-01-12
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Expires: 2000-12-02
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Abstract

Abstract Copolymeric organopolysiloxanes comprising SiO 2 are prepared by forming an acidic, homogeneous mixture of a silanol-containing resinous copolymeric siloxane comprising R 3 SiO 1/2 siloxane units and SiO 2 siloxane units, an organohydrogenpolysiloxane and an organic solvent and heating the resulting mixture to remove substantially all of the organic solvent. The copolymeric organosiloxanes contain silicon-bonded hydroxyl radicals and/or silicon-bonded hydrogen radicals in varying amounts which depends upon the acidity of the homogeneous mixture that is formed and the ratio of silicon-bonded hydrogen radicals to silicon-bonded hydroxyl radicals therein. The copolymeric organopolysiloxanes are useful as a reactive component in various types of curable silicone compositions.

Inventors

  • 👤 John D. Blizzard
  • 👤 Terence J. Swihart

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-09 14:42
CPC Classifications
C; C08; C08G; C08G77/00; C08G77/42; C08G77/44; C08L; C08L83/00; C08L83/04; C08G77/04; C08G77/12; C08G77/14; C08G77/16

Claims Analysis

Total Claims: 13
Claim 1
Independent Claim 140 words
A method for preparing a liquid copolymeric organopolysiloxane, said method comprising (A) forming a homogeneous mixture having an acid number greater than zero and comprising (a) an organic solvent solution of a resinous copolymeric siloxane containing silicon-bonded hydroxyl radicals and consisting essentially of R 3 SiO 1/2 siloxane units and SiO 4/2 siloxane units wherein the ratio of the number of said R 3 SiO 1/2 siloxane units to the number of said SiO 4/2 siloxane units has a value of from 0.6/1 to 0.9/1 and each R denotes, independently, a monovalent hydrocarbon radical and (b) a liquid organohydrogenpolysiloxane wherein each organic radical is, independently, a monovalent hydrocarbon radical, there being an average of at least one silicon-bonded hydrogen radical per molecule of said organohydrogenpolysiloxane, and (B) heating said homogeneous mixture to remove substantially all of said organic solvent therefrom.
Claim 2
Independent Claim 140 words
A method for preparing a liquid copolymeric organopolysiloxane, said method comprising (A) forming a homogeneous mixture having an acid number greater than zero and comprising (a) an organic solvent solution of a resinous copolymeric siloxane containing silicon-bonded hydroxyl radicals and consisting essentially of R 3 SiO 1/2 siloxane units and SiO 4/2 siloxane units wherein the ratio of the number of said R 3 SiO 1/2 siloxane units to the number of said SiO 4/2 siloxane units has a value of from 0.6/1 to 0.9/1 and each R denotes, independently, a monovalent hydrocarbon radical and (b) a liquid organohydrogenpolysiloxane wherein each organic radical is, independently, a monovalent hydrocarbon radical, there being an average of at least one silicon-bonded hydrogen radical per molecule of said organohydrogenpolysiloxane, and (B) heating said homogeneous mixture to remove substantially all of said organic solvent therefrom.
Claim 3
Dependent Claim 32 words
A method according to claim 1 wherein the homogeneous mixture is sufficiently acidic to provide an acid number of from 0.1 to 1 for the homogeneous mixture, extrapolated to the solvent-free state.
Claim 4
Dependent Claim 39 words
A method according to claim 2 wherein the ratio of the total number of silicon-bonded hydrogen atoms in component (b) to the total number of silicon-bonded hydroxyl radicals in component (a) has a value of at least about 2.
Claim 5
Dependent Claim 52 words
A method according to claim 1, 2 or 3 wherein the resinous copolymeric siloxane consists of (CH 3 ) 3 SiO 1/2 siloxane units and SiO 4/2 siloxane units and has a silicon-bonded hydroxy content of from 1 to 5 percent by weight and an acid number of from 0.3 to 1.4.
Claim 6
Dependent Claim 58 words
A method according to claim 4 wherein the organohydrogenpolysiloxane has the formula (R")(CH 3 ) 2 SiO{(CH 3 ) 2 SiO} a {(CH 3 )(H)SiO} b Si(CH 3 ) 2 (R") wherein each R" denotes, independently, a methyl radical or a hydrogen radical and a and b denote numbers, each having an average value of zero or more.
Claim 7
Dependent Claim 35 words
A method according to claim 5 wherein the organohydrogenpolysiloxane has the formula (CH 3 ) 3 SiO{(CH 3 )(H)SiO} b Si(CH 3 ) 3 wherein b has an average value of from 30 to 70.
Claim 8
Dependent Claim 32 words
A method according to claim 6 wherein the homogeneous mixture contains from 40 to 60 parts by weight of resinous copolymeric siloxane and from 40 to 60 parts by weight of organohydrogenpolysiloxane.
Claim 9
Dependent Claim 13 words
A copolymeric organopolysiloxane prepared by the method of claims 1, 2, or 3.
Claim 10
Dependent Claim 10 words
A copolymeric organopolysiloxane prepared by the method of claim 4.
Claim 11
Dependent Claim 10 words
A copolymeric organopolysiloxane prepared by the method of claim 5.
Claim 12
Dependent Claim 10 words
A copolymeric organopolysiloxane prepared by the method of claim 6.
Claim 13
Dependent Claim 10 words
A copolymeric organopolysiloxane prepared by the method of claim 7.

References Cited (Backward Citations)

US3205283A Cited
US2676182A Cited
US2814601A Cited
US3627851A Cited
US3772247A Cited
US3992426A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1985-01-11 1985-07-13 1986-01-12 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1989-01-11 1989-07-13 1990-01-12 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1993-01-11 1993-07-13 1994-01-12 $7700.00 Window Closed / Lapsed

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