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US4599367A Expired / Lapsed US ⏱️ 0.0 years remaining

Water-blown silicone foam

Assignee: Dow Silicones Corp
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Filing: 1985-10-16
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Granted: 1986-07-08
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Expires: 2005-10-16
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Abstract

Abstract This invention relates to a method of producing silicone elastomeric foam of low density. The method mixes polydiorganosiloxanes having hydroxyl endblocking or vinyl endblocking or mixtures of both along with water to react with silicon hydride in the presence of platinum catalyst to release hydrogen gas to create a froth which cures to a foam. The combination of ingredients allows the manufacture of silicone foam having different combinations of properties than those obtained from previous methods. Embodiments of the invention also make use of specific profoamers and specific alcohols to further modify the properties of the foams produced. The method of this invention yields a low cost, low density, silicone elastomeric foam having physical properties which enable it to be used in cushioning and sealing applications.

Inventors

  • 👤 Therese M. Bauman
  • 👤 John E. Dietlein

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-29 10:31
CPC Classifications
C; C08; C08J; C08J9/00; C08J9/02; C08J9/04; C08J9/12; C08L; C08L83/00; C08L83/04; C08J2383/00; C08J2383/04

Claims Analysis

Total Claims: 14
Claim 1
Independent Claim 565 words
A method of producing an open-cell silicone foam at room temperature consisting of (A) mixing ingredients consisting essentially of (1) 100 parts by weight of a polydiorganosiloxane having organic groups selected from the group consisting of methyl, ethyl, propyl, vinyl, phenyl, and 3,3,3-trifluoropropyl, endblocking consisting of hydroxyl or vinyl groups, and a viscosity of from 0.4 to 100 Pa.sup.. s at 25° C., (2) from 15 to 50 parts by weight of a silicon hydride of the formula ##STR5## where R is an alkyl radical of 1 to 4 carbon atoms or phenyl and R 1 is R or hydrogen, x and y are such that x is from 0 to 40 percent of y, y is at least 3, and x plus y are such that the viscosity of the silicon hydride is below 0.05 Pa.sup.. s at 25° C., (3) from 0.5 to 15 parts by weight of water, (4)from 10 to 100 parts by weight of platinum per million parts of (A) in the form of a platinum catalyst, (5) optionally a profoamer consisting essentially of a resinous, benzene-soluble organosiloxane copolymer consisting essentially of SiO 4/2 units, silicon-bonded hydroxyl groups, (CH 3 ) 3 SiO 1/2 units and fluorine-containing units selected from the group consisting of R a R b 'SiO.sub.(4-a-b)/2 and R"[Si(R') b O.sub.(3-b)/2 ] 2 and mixtures thereof, where R is a monovalent organic radical containing at least four perfluorinated carbon atoms and is bonded to the silicon atom of said fluorine-containing units by a sequence of at least two methylene units or by an oxygen atom that is, in turn, bonded to a sequence of at least two methylene units, R' is an alkyl radical containing from 1 to 3 carbon atoms, and R" is a divalent organic radical containing at least four perfluorinated carbon atoms and is bonded to the silicon atom of said fluorinecontaining units by means of a carbon or oxygen atom, a is 1 or 2, b is 0, 1 or 2 and the sum of a and b is 3 or less with the provision that when R and R" represent fluorine-containing units bonded to silicon via an oxygen atom the organosiloxane copolymer optionally contains repeating units of the formula GSiO 3/2 where G represents the residue obtained by removal of the hydrogen atom from a hydroxyl group of a linear organic polymer containing an average of at least one terminal hydroxyl group per molecule and selected from the group consisting of polyethers, polyoxyalkylene glycols, homopolymers of ethylenically unsaturated alcohols and copolymers of ethylenically unsaturated alcohols with ethylenically unsaturated hydrocarbons; the molar ratio of all units other than hydroxyl and SiO 4/2 units to SiO 4/2 units is from 0.7:1 to 1.1:1, inclusive, and the concentration of said fluorinecontaining units and any GSiO 3/2 units is sufficient to (a) impart a surface tension of less than 2.2×10 -4 newtons per centimeter at 25° C. to a 10 percent by weight solution of (5) in a hydroxyl endblocked polydimethylsiloxane exhibiting a viscosity of 0.08 Pa.s at 25° C., and (b) require the addition of from 0 to 100 percent by weight of xylene to said 10 percent by weight solution to achieve optical clarity, and (6) optionally an alcohol having from 1 to 12 carbon atoms, and (B) allowing the mixture to form a froth and cure at ambient temperature to an elastomeric silicone foam.
Claim 2
Independent Claim 565 words
A method of producing an open-cell silicone foam at room temperature consisting of (A) mixing ingredients consisting essentially of (1) 100 parts by weight of a polydiorganosiloxane having organic groups selected from the group consisting of methyl, ethyl, propyl, vinyl, phenyl, and 3,3,3-trifluoropropyl, endblocking consisting of hydroxyl or vinyl groups, and a viscosity of from 0.4 to 100 Pa.sup.. s at 25° C., (2) from 15 to 50 parts by weight of a silicon hydride of the formula ##STR5## where R is an alkyl radical of 1 to 4 carbon atoms or phenyl and R 1 is R or hydrogen, x and y are such that x is from 0 to 40 percent of y, y is at least 3, and x plus y are such that the viscosity of the silicon hydride is below 0.05 Pa.sup.. s at 25° C., (3) from 0.5 to 15 parts by weight of water, (4)from 10 to 100 parts by weight of platinum per million parts of (A) in the form of a platinum catalyst, (5) optionally a profoamer consisting essentially of a resinous, benzene-soluble organosiloxane copolymer consisting essentially of SiO 4/2 units, silicon-bonded hydroxyl groups, (CH 3 ) 3 SiO 1/2 units and fluorine-containing units selected from the group consisting of R a R b 'SiO.sub.(4-a-b)/2 and R"[Si(R') b O.sub.(3-b)/2 ] 2 and mixtures thereof, where R is a monovalent organic radical containing at least four perfluorinated carbon atoms and is bonded to the silicon atom of said fluorine-containing units by a sequence of at least two methylene units or by an oxygen atom that is, in turn, bonded to a sequence of at least two methylene units, R' is an alkyl radical containing from 1 to 3 carbon atoms, and R" is a divalent organic radical containing at least four perfluorinated carbon atoms and is bonded to the silicon atom of said fluorinecontaining units by means of a carbon or oxygen atom, a is 1 or 2, b is 0, 1 or 2 and the sum of a and b is 3 or less with the provision that when R and R" represent fluorine-containing units bonded to silicon via an oxygen atom the organosiloxane copolymer optionally contains repeating units of the formula GSiO 3/2 where G represents the residue obtained by removal of the hydrogen atom from a hydroxyl group of a linear organic polymer containing an average of at least one terminal hydroxyl group per molecule and selected from the group consisting of polyethers, polyoxyalkylene glycols, homopolymers of ethylenically unsaturated alcohols and copolymers of ethylenically unsaturated alcohols with ethylenically unsaturated hydrocarbons; the molar ratio of all units other than hydroxyl and SiO 4/2 units to SiO 4/2 units is from 0.7:1 to 1.1:1, inclusive, and the concentration of said fluorinecontaining units and any GSiO 3/2 units is sufficient to (a) impart a surface tension of less than 2.2×10 -4 newtons per centimeter at 25° C. to a 10 percent by weight solution of (5) in a hydroxyl endblocked polydimethylsiloxane exhibiting a viscosity of 0.08 Pa.s at 25° C., and (b) require the addition of from 0 to 100 percent by weight of xylene to said 10 percent by weight solution to achieve optical clarity, and (6) optionally an alcohol having from 1 to 12 carbon atoms, and (B) allowing the mixture to form a froth and cure at ambient temperature to an elastomeric silicone foam.
Claim 3
Dependent Claim 22 words
The method of claim 1 in which (1) comprises a polydiorganosiloxane having hydroxyl endblocking groups and a polydiorganosiloxane having vinyl endblocking groups.
Claim 4
Dependent Claim 21 words
The method of claim 1 in which (2) is present in an amount of from 15 to 30 parts by weight.
Claim 5
Dependent Claim 21 words
The method of claim 3 in which the silicon hydride is such that x is less than 5 percent of y.
Claim 6
Dependent Claim 21 words
The method of claim 1 in which (3) is present in an amount of from 1 to 5 parts by weight.
Claim 7
Dependent Claim 21 words
The method of claim 2 in which (2) is present in an amount of from 15 to 30 parts by weight.
Claim 8
Dependent Claim 21 words
The method of claim 2 in which (3) is present in an amount of from 1 to 5 parts by weight.
Claim 9
Dependent Claim 23 words
The method of claim 1 in which the profoamer (5) is present in an amount of from 1 to 10 parts by weight.
Claim 10
Dependent Claim 93 words
The method of claim 1 in which the fluorine-containing units of (5) are of the formula R a R b 'SiO.sub.(4-a-b)/2 where R is F(C n F 2n )(CH 2 ) 2 O c ; R' is methyl; a is 1; b is 0, 1, or 2; c is 0 or 1 and wherein each of said fluorine-containing units n represents an integer that is the same or different with respect to the value of n in other fluorine-containing units of (5), the average value of n being from 4 to 20 inclusive.
Claim 11
Dependent Claim 23 words
The method of claim 1 in which the alcohol (6) is present in an amount of from 1 to 5 parts by weight.
Claim 12
Dependent Claim 12 words
The method of claim 10 in which the alcohol is lauryl alcohol.
Claim 13
Dependent Claim 11 words
The method of claim 10 in which the alcohol is normal-propanol.
Claim 14
Dependent Claim 38 words
The method of claim 1 in which the ingredients are first mixed in two parts for storage purposes: ingredient (4) being in one part with all or part of (1) and ingredient (2) being in the other part.

References Cited (Backward Citations)

US3070555A Cited
US3428580A Cited
US3425967A Cited
US3923705A Cited
US4026845A Cited
US4026843A Cited
US4189545A Cited
GB2065661A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1989-07-07 1990-01-06 1990-07-08 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1993-07-07 1994-01-06 1994-07-08 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1997-07-07 1998-01-06 1998-07-08 $7700.00 Window Closed / Lapsed

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