Preparation of organopolysiloxane resins with weak organic bases

Claim 2

In a process for preparing an organopolysiloxane by hydrolyzing a hydrolyzable silane in an aqueous solution containing at least the stoichiometric amount of water required for said hydrolysis and having an acid pH, and then condensing the hydrolyzed silane to the organopolysiloxane, the improvements comprising incorporating in said aqueous solution after hydrolysis of said silane and prior to complete condensation and polymerization of the organopolysiloxane to a solid state, a stabilizing amount against gelation of a weak organic base having an ionization constant in water no greater than about 1×10 -7 at 25° C. to at least partially neutralize the acid of said water and provide improved stability to said organopolysiloxane against gelation.

Claim 3

The process of claim 1 in which the molar ratio of said water to said hydrolyzable silane is within the range of about 1.5:1 to about 10:1, respectively.

Claim 4

The process of claim 1 in which said hydrolyzable silane corresponds to the formula: T.sub.n SiZ.sub.(4-n) in which T is a monovalent hydrocarbon radical, Z is hydroxyl or a monovalent hydrolyzable group, and n is a whole number less than four.

Claim 5

The process of claim 1 in which said hydrolyzable silane corresponds to the formula: T.sub.n SiZ.sub.(4-n) in which T is alkyl, alkenyl, or aryl, each of less than seven carbon atoms, z is hydroxyl, alkoxy less than seven carbon atoms, acyloxy less than seven carbon atoms, or halogen and n is a whole number less than four.

Claim 6

The process of claim 1 in which said hydrolyzable silane is a hydrolyzable trialkoxysilane in which any alkoxy substituent contains from one to about six carbon atoms.

Claim 7

The process of claim 1 in which said hydrolyzable silane corresponds to the formula: RSi(OR.sub.1).sub.3 in which R is alkyl from one to about six carbon atoms or phenyl, and R 1 is alkyl from one to about six carbon atoms.

Claim 8

The process of claim 1 in which said condensing is by heating of the solution at a temperature within the range of about 40° to about 300° C. for about one hour to about ten hours.

Claim 9

The process of claim 1 in which said weak organic base is a trivalent, nitrogen-containing organic base.

Claim 10

The process of claim 1 in which said weak organic base is selected from the group consisting of quinoline, aniline, benzidine, acetanilide, pyridine, and toluidine.

Claim 11

The process of claim 1 in which said weak organic base is quinoline.

Claim 12

The process of claim 1 in which said stabilizing amount of said weak organic base is within the range of about 5 ppm to about 1.5% by weight of said aqueous solution.

Claim 13

The process of claim 1 in which said ionization constant is within the range of about 1×10 -7 to about 1×10 -14 .

Claim 14

The process of claim 1 including forming the organopolysiloxane to a desired shape, and then heating to cure the organopolysiloxane to a thermoset form having said shape.

Claim 15

A process for preparing an organopolysiloxane solution having improved stability against gelation, comprising: (a) hydrolyzing in aqueous solution a hydrolyzable silane corresponding to the formula: T.sub.n SiZ.sub.(4-n) in which T is a monovalent hydrocarbon radical, Z is hydroxyl or a monovalent hydrolyzable group, and n is a whole number less than four, (b) said aqueous solution having a molar ratio of water to hydrolyzable silane within the range of about 1.5:1 to about 5:1, respectively, (c) heating said solution to condense the hydrolyzed silane and polymerize it to an organopolysiloxane, and (d) adding to said aqueous solution subsequently to said hydrolysis of the hydrolyzable silane and prior to complete condensation and polymerization of the organopolysiloxane to a solid state a stabilizing amount against gelation of a trivalent, nitrogen-containing weak organic base having an ionization constant in water at 25° C. within the range of about 1×10 -7 to about 1×10 -14 .

Claim 16

A process for preparing an organopolysiloxane solution having improved stability against gelation, comprising: (a) hydrolyzing in aqueous solution a hydrolyzable silane corresponding to the formula: T.sub.n SiZ.sub.(4-n) in which T is a monovalent hydrocarbon radical, Z is hydroxyl or a monovalent hydrolyzable group, and n is a whole number less than four, (b) said aqueous solution having a molar ratio of water to hydrolyzable silane within the range of about 1.5:1 to about 5:1, respectively, (c) heating said solution to condense the hydrolyzed silane and polymerize it to an organopolysiloxane, and (d) adding to said aqueous solution subsequently to said hydrolysis of the hydrolyzable silane and prior to complete condensation and polymerization of the organopolysiloxane to a solid state a stabilizing amount against gelation of a trivalent, nitrogen-containing weak organic base having an ionization constant in water at 25° C. within the range of about 1×10 -7 to about 1×10 -14 .

Claim 17

The process of claim 14 in which said trivalent, nitrogen-containing organic base is selected from the group consisting of quinoline, aniline, benzidine, acetanilide, pyridine, and toluidene.

Claim 18

An organopolysiloxane resulting from the process of claim 1, said organopolysiloxane being still soluble in ethanol after about two months at room temperature.

Claim 19

An organopolysiloxane resulting from the process of claim 14, said organopolysiloxane being still soluble in ethanol after about two months at room temperature.

Claim 20

An organic solvent-soluble siloxane partial condensation product resulting from the process of claim 1, said condensation product still being soluble in ethanol after about two months at room temperature.

Claim 21

A composition adapted for shaping into a desired form comprising a solution containing an organic solvent-soluble siloxane partial condensation product resulting from the process of claim 1, the amount of said siloxane condensation product not exceeding 90 weight percent of said solution, said condensation product being still soluble in ethanol after about two months at room temperature.

Claim 22

A composition adapted for shaping to a desired form comprising a solution containing an organic solvent-soluble siloxane partial condensation product resulting from the process of claim 14, the amount of said siloxane condensation product not exceeding 90 weight percent of said solution, said condensation product being still soluble in ethanol after about two months at room temperature.