Non-flammable and optionally electrically conductive organo-silicate polymers and process for preparing same

Claim 2

In a process for preparing organosilicate polymers by reaction of a water glass solution with an isocyanate compound having at least two isocyanate groups, the improvement which comprises admixing with the water glass solutions prior to the introduction of said isocyanate compound into the reaction mixture, a zwitterion compound having in the molecule at least one group with positive charge, at least one group with negative charge, and additionally at least one hydrogen atom with Zerewitinov activity, the zwitterion compound being a tertiary amino compound of the general formula ##STR7## wherein the radicals R 1 , R 2 and R 3 stand for hydrogen atoms or a radical of the general formula ##STR8## wherein n is an integer from 1 to 25 and the radicals X 1 and X 2 are hydrogen atoms and/or alkyl radicals with 1 to 25 carbon atoms, the radicals R 1 , R 2 and R 3 may be different, at best two of the radicals R 1 , R 2 or R 3 may be hydrogen atoms, and the alkyl radicals may bear primary and/or secondary hydroxyl groups.

Claim 3

Process according to claim 1 characterized in that the ratio of solids in the water glass solution employed to the isocyanate groups employed is within a range of 0.1 to 6, based on the percentage of NCO groups and the dry weight of the water glass.

Claim 4

Process according to claim 1 characterized in that as catalyst a tertiary amino compound of the general formula ##STR9## is used wherein the radicals R 1 , R 2 and R 3 stand for hydrogen atoms or a radical of the general formula ##STR10## wherein the radicals X 1 and/or X 2 are hydrogen atoms, alkyl radicals having from 1 to 25 carbon atoms, or the radical --(CH 2 ) m OH with m being an integer from 0 to 25, at best two of the radicals R 1 , R 2 or R 3 may be hydrogen atoms, and at least one of the radicals R 1 , R 2 , R 3 must bear a hydroxyl group.

Claim 5

Process according to claim 1 characterized in that the reaction is carried out in the presence of 2,4,6-tris(dimethylaminomethyl)phenol or of 2,4,6-tris(ethyl-2-hydroxy-ethyl-aminomethyl)phenol and optionally dibutyltin dilaurate.

Claim 6

Process according to claim 1 characterized in that the reaction is carried out in the additional presence of a compound acting as water glass hardening agent and lowering the pH of the reaction mixture.

Claim 7

Process according to claim 5 characterized in that the water glass hardening agent is a metal silicofluoride.

Claim 8

Process according to claim 1 characterized in that the reaction is carried out in the presence of one or more emulsifiers.

Claim 9

Process according to claim 1 characterized in that the reaction is carried out in the presence of volatile propellants.

Claim 10

Process according to claim 1 characterized in that the reaction is carried out in the presence of gas-evolving propellants.

Claim 11

Process according to claim 1 characterized in that the reaction is carried out in the additional presence of flame retarding agents, especially in the presence of halogenated phosphoric acid esters.

Claim 12

Process according to claim 1 characterized in that the reaction is carried out in the presence of fillers and/or pigments.

Claim 13

Process according to claim 11 characterized in that diatomaceous earth is used as filler.

Claim 14

Process according to claim 1 characterized in that the reaction is carried out in the presence of a polyester and/or polyether.

Claim 15

Process according to claim 1 characterized in that the isocyanate component is a mixture of polyisocyanates containing substantially no diisocyanates and monoisocyanates and wherein said mixture is the fraction 1 obtained by the process for the separation of an organic polysocyanate mixture which contains, in preponderant amount, the diphenyl-methane-diisocyanate isomers and higher functional polyisocyanates with more than two benzene rings in the molecule, characterised in that first the organic polyisocyanate mixture is separated by a short-path distillation into a fraction 1, which besides a residue of diphenyl-methane diisocyanate isomers, contains the higher functional polyisocyanates with more than two benzene rings in the molecule, and into a fraction 2, which of the polyisocyanates, contains practically only the diphenyl-methane-diisocyanate isomers, and then the fraction 2 is separated by fractional crystallisation into the fraction 3, which preferably has a content of at least 98% 4,4'-diphenyl-methane-diisocyanate, and the fraction 4, in which the 2,2'-and 2,4'-isomers of the diphenyl-methane-diisocyanate are enriched in the 4,4'-diphenyl-methane-diisocyanate.

Claim 16

Process according to claim 1 characterized in that prior to the reaction a synthetic resin dispersion, is added to one of the starting components.

Claim 17

Process according to claim 1 characterized in that said water glass solution is an aqueous sodium silicate solution of 48° to 50° Be.

Claim 18

Process according to claim 1 characterized in that the isocyanate component is an undistilled crude isocyanate product as obtained after phosgenation of crude aniline/formaldehyde resins.

Claim 19

Process according to claim 7 wherein the emulsifier is an alkylphenol oxyethylate having an oxethylating degree of 9 to 10.