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Silicone compositions and uses thereof

  • US 5,777,059 A
  • Filed: 04/19/1996
  • Issued: 07/07/1998
  • Est. Priority Date: 04/19/1996
  • Status: Expired due to Term
First Claim
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1. A silicone composition prepared by reacting at a temperature of 25°

  • C. to 300°

    C. a mixture comprising;

    (i) 1 to 100 parts by weight of a polyisobutylene compound;

    (ii) 5 to 100 parts by weight of a polyorganosiloxane having a viscosity of 200 to about 100 million mm2 /s at 25°

    C. expressed by the general formula R1a (R2 O)b SiO.sub.(4-a-b)/2 in which R1 a monovalent hydrocarbon or halogenated hydrocarbon group having 1 to 10 carbon atoms, R2 is hydrogen or a monovalent hydrocarbon group having 1 to 10 carbon atoms, a has an average value of 1.9 to 2.2 and b has a sufficiently large value to give at least one --OR2 group in each molecule, at least one such --OR2 group being present at the end of the molecular chain;

    (iii) 0.5 to 20 parts by weight of at least one silicon compound selected from(a) an organosilicon compound of the general formula R3c SiX4-c in which R3 is a monovalent hydrocarbon group having 1 to 5 carbon atoms, X is selected from a halogen atom or a hydrolyzable group and c has an average value of one or less,(b) a partially hydrolyzed condensate of said compound (a),(c) a siloxane resin comprising (CH3)3 SiO1/2 units and SiO4 /2 units wherein the ratio of (CH3)3 SiO1/2 units to SiO4/2 units is 0.4;

    1 to 1.2;

    1, or(d) a condensate of said compound (c) with said compound (a) or (b); and

    (iv) a catalytic amount of a catalyst selected from the group consisting of alkali metal hydroxides, alkali metal silanolates, alkali metal alkoxides, guatemary ammonium hydroxides, quatemary ammonium silanolates, quatemnar phosphonium hydroxides, quatemmry phosphonium silanolates, mineral acids, acetic acid, organosulfonic acids, ammonium carbonate, and ammonium hydroxide.

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