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US4448927A Expired / Lapsed US ⏱️ 0.0 years remaining

Method of polymerizing oligomers of polydiorganosiloxane in the presence of filler

Assignee: Dow Silicones Corp
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Filing: 1983-03-14
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Granted: 1984-05-15
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Expires: 2003-03-14
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Abstract

Abstract Oligomers of low molecular weight polydiorganosiloxanes, polydiorganocyclosiloxanes, or mixtures are polymerized in the presence of acidic or neutral reinforcing fillers. Trifluoromethane sulfonic acid is used as the polymerization catalyst. The method can also include endblocked polydiorganosiloxane to control the molecular weight of the silicone polymer in the silicone polymer-filler produced. The method combines the oligomer and filler, heats to from about 70° to 150° C., adds catalyst, adjusts temperature, and polymerizes the mixture, then inactivates with a Lewis base such as calcined magnesium oxide. The non-crepeing silicone polymer-filler mixture which is the product of the method is usable as electrical insulation grease, or as a reinforced polymer mixture useful in producing silicone elastomers. The mixture can be mixed with curing agents to produce heat curable and moisture curable elastomeric compositions.

Inventors

  • 👤 James R. Falender
  • 👤 John C. Saam

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-30 03:32
CPC Classifications
C; C08; C08G; C08G77/00; C08G77/04; C08G77/06

Claims Analysis

Total Claims: 25
Claim 1
Independent Claim 262 words
A method of polymerizing oligomer in the presence of reinforcing filler comprising (A) mixing (i) 100 parts by weight of oligomer selected from the group consisting of polydiorganosiloxane (a) of the formula HO(R.sub.2 SiO).sub.x H, polydiorganocyclosiloxane (b) of the formula ##STR2## and mixtures thereof, optionally (i) can have present oligomer selected from the group consisting of polydiorganosiloxane (c) of the formula R'.sub.3 SiO(R.sub.2 SiO).sub.z SiR'.sub.3, polydiorganosiloxane (d) of the formula R'.sub.3 SiO(R.sub.2 SiO).sub.z H, and mixtures thereof wherein each R is a radical selected from the group consisting of methyl, ethyl, propyl, phenyl, vinyl, allyl, and 3,3,3-trifluoropropyl; each R' is monovalent hydrocarbon radical of 6 or less carbon atoms, x is an average value in the range of from 3 to 50, y is an average value in the range of from 3 to 10, and z is an average value in the range of from 0 to 50 inclusive; with (ii) from 2 to 70 parts by weight of reinforcing filler which is acidic or neutral, to yield a paste-type material, (B) intiating polymerization of (A) in a closed system at a temperature in the range of 70° C. to 150° C. with from 400 to 4000 parts by weight trifluoromethane sulfonic acid per million parts by weight of (i), then agitating the resulting product of (B) adjusting its temperature to a value in the range of 20° C. to 100° C., polymerizing until the desired increase in molecular weight is reached, then (D) admixing a Lewis base to inactivate the trifluoromethane sulfonic acid and produce a non-crepeing silicone polymer-filler mixture.
Claim 2
Independent Claim 262 words
A method of polymerizing oligomer in the presence of reinforcing filler comprising (A) mixing (i) 100 parts by weight of oligomer selected from the group consisting of polydiorganosiloxane (a) of the formula HO(R.sub.2 SiO).sub.x H, polydiorganocyclosiloxane (b) of the formula ##STR2## and mixtures thereof, optionally (i) can have present oligomer selected from the group consisting of polydiorganosiloxane (c) of the formula R'.sub.3 SiO(R.sub.2 SiO).sub.z SiR'.sub.3, polydiorganosiloxane (d) of the formula R'.sub.3 SiO(R.sub.2 SiO).sub.z H, and mixtures thereof wherein each R is a radical selected from the group consisting of methyl, ethyl, propyl, phenyl, vinyl, allyl, and 3,3,3-trifluoropropyl; each R' is monovalent hydrocarbon radical of 6 or less carbon atoms, x is an average value in the range of from 3 to 50, y is an average value in the range of from 3 to 10, and z is an average value in the range of from 0 to 50 inclusive; with (ii) from 2 to 70 parts by weight of reinforcing filler which is acidic or neutral, to yield a paste-type material, (B) intiating polymerization of (A) in a closed system at a temperature in the range of 70° C. to 150° C. with from 400 to 4000 parts by weight trifluoromethane sulfonic acid per million parts by weight of (i), then agitating the resulting product of (B) adjusting its temperature to a value in the range of 20° C. to 100° C., polymerizing until the desired increase in molecular weight is reached, then (D) admixing a Lewis base to inactivate the trifluoromethane sulfonic acid and produce a non-crepeing silicone polymer-filler mixture.
Claim 3
Dependent Claim 73 words
The method of claim 1 in which the reinforcing filler is fumed silica, the resulting mixture of step (A) is heated in a closed system to a temperature of from 100° C. to 200° C. for a time sufficient to remove any free water, removing such water from the system; then continuing with step (B), adjusting, if necessary, the temperature to from 100° C. to 150° C. before adding the trifluoromethane sulfonic acid.
Claim 4
Dependent Claim 48 words
The method of claim 2 in which x is from 10 to 50, y is from 3 to 6, the amount of trifluoromethane sulfonic acid is from 500 to 1500 parts by weight per million parts by weight of (i), and the Lewis base is calcined magnesium oxide.
Claim 5
Dependent Claim 50 words
The method of claim 3 in which the temperature is reduced during step (C) to a range of from 20° to 30° C., water is removed, and the polymerization is continued to yield a silicone polymer-filler mixture in which the polymer has a degree of polymerization of greater than 1000.
Claim 6
Dependent Claim 28 words
The method of claim 4 in which the silicone polymer-filler mixture is further mixed with an organic peroxide suitable for curing silicone elastomers to yield a curable composition.
Claim 7
Dependent Claim 47 words
The method of claim 4 in which the resulting mixture of step (A) is heated to a temperature of from 140° C. to 170° C., then adjusted to a temperature of from 110° C. to 140° C. before addition of the trifluoromethane sulfonic acid in step (B).
Claim 8
Dependent Claim 28 words
The method of claim 6 in which the silicone polymer-filler mixture is further mixed with an organic peroxide suitable for curing silicone elastomers to yield a curable composition.
Claim 9
Dependent Claim 19 words
The method of claim 1 in which from 0.01 to 2.0 percent of R plus R' are vinyl radicals.
Claim 10
Dependent Claim 43 words
The method of claim 8 in which the vinyl radicals are derived from polydiorganosiloxane (c), z is from 0 to 21, the reinforcing filler is from 5 to 20 parts by weight of fumed silica, and the Lewis base is calcined magnesium oxide.
Claim 11
Dependent Claim 102 words
The method of claim 9 in which the silicone polymer-filler mixture is further mixed with a curing agent comprising an organohydrogensiloxane in sufficient amount to provide at least one silicone-bonded hydrogen atom per vinyl radical in (i), said organohydrogensiloxane having an average of at least three silicon-bonded hydrogen atoms per molecule and having units selected from the group consisting of methylhydrogensiloxane, dimethylsiloxane, dimethylhydrogensiloxy, trimethylsiloxy, and SiO 2 units; and an amount of a platinum catalyst in an amount sufficient to provide at least one part by weight of platinum per million parts by weight of silicone polymer in the silicone polymer-filler mixture.
Claim 12
Dependent Claim 12 words
The non-crepeing silicone polymer-filler mixture produced by the method of claim 1.
Claim 13
Dependent Claim 10 words
The curable composition produced by the method of claim 5.
Claim 14
Dependent Claim 10 words
The curable composition produced by the method of claim 7.
Claim 15
Dependent Claim 10 words
The curable composition produced by the method of claim 10.
Claim 16
Dependent Claim 11 words
The cured product obtained by heating the composition of claim 12.
Claim 17
Dependent Claim 11 words
The cured product obtained by curing the composition of claim 14.
Claim 18
Dependent Claim 50 words
The method of claim 8 in which (i) is the polydiorganocyclosiloxane (b), y having an average value of from 3 to 6, the vinyl radicals are derived from polydiorganosiloxane (c), z is from 0 to 21, the reinforcing filler is fumed silica, and the Lewis base is calcined magnesium oxide.
Claim 19
Dependent Claim 29 words
The method of claim 17 in which the non-crepeing silicone polymer-filler mixture is further mixed with an organic peroxide suitable for curing silicone elastomers to yield a curable composition.
Claim 20
Dependent Claim 105 words
The method of claim 17 in which the non-crepeing silicone polymer-filler mixture is further mixed with a curing agent comprising an organohydrogensiloxane in sufficient amount to provide at least one silicone-bonded hydrogen atom per vinyl radical in (i), said organohydrogensiloxane having an average of greater then two silicon-bonded hydrogen atoms per molecule and having units selected from the group consisting of methylhydrogensiloxane, dimethylsiloxane, dimethylhydrogensiloxy, trimethylsiloxy, SiO 2 units, and mixtures thereof; and an amount of a platinum catalyst in an amount sufficient to provide at least one part by weight of platinum per million parts by weight of silicone polymer in the silicone polymer-filler mixture.
Claim 21
Dependent Claim 10 words
The curable composition produced by the method of claim 18.
Claim 22
Dependent Claim 10 words
The curable composition produced by the method of claim 19.
Claim 23
Dependent Claim 23 words
The method of claim 1 in which the non-crepeing silicone polymer-filler mixture is further mixed with curing agent to yield a curable composition.
Claim 24
Dependent Claim 23 words
The method of claim 22 in which the curing agent is a moisture sensitive crosslinker and the curable composition cures at room temperature.
Claim 25
Dependent Claim 10 words
The curable composition produced by the method of claim 23.

References Cited (Backward Citations)

US3447988A Cited
GB1325654A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1987-05-15 1987-11-14 1988-05-15 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1991-05-15 1991-11-14 1992-05-15 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1995-05-15 1995-11-14 1996-05-15 $7700.00 Window Closed / Lapsed

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