Polythioether polyurethanes and their preparation

Abstract

Novel polythioether polyurethanes of superior thermal and oxidative aging stability are prepared from polythioether dithiols derived from addition of dithiols to acetylenes under free radical conditions. These polythioether dithiols having alkyl branching contain the divalent alkylene groups derived from their dithiol and acetylene monomer components in a regularly alternating manner. This dithiol is reacted with an epoxide with an amine catalyst to form a polythioether diol of the formula ##STR1## wherein R is a C.sub.1 -C.sub.30 divalent organic radical, R' is selected from the group consisting of H, C.sub.1 -C.sub.30 alkyl, C.sub.2 -C.sub.30 alkenyl, C.sub.2 -C.sub.30 alkynyl, C.sub.7 -C.sub.20 aralkyl and mixtures thereof, provided that either R has a branched structure or R' is alkyl, R" is H or methyl and n is 2 to 1000. These polythioether diols are chain extended and crosslinked via reactions with organic diisocyanates of the formula R'" (NCO).sub.2 to yield polythioether polyurethanes of the repeating structure: ##STR2## wherein R, R', R" and n are as defined above and R"' is phenylene, tolylene, xylylene, diphenylmethane, chlorophenylene and C.sub.2 to C.sub.12 polymethylene. These polythioether polyurethanes possess superior thermal and oxidative aging stability.

Dependencies are inferred from the claim text.