The thermal and photodegradation of a number of linear polysulfide (LP) prepolymers H(SC2H4OCH2OC2H4S)(n)H have been studied by H-1 and C-13 NMR spectroscopy, IR spectroscopy, gel permeation chromatography (GPC) and particularly, by electrospray ionisation mass spectrometry (ESI). ESI results point to the important role of hydrolytic pathways leading to the elimination of CH2O and the formation of hydroxy-terminated products, followed by the reduction of disulfide groups by CH2O. This conclusion is supported by the observation of very slow degradation by heat or UV-light of an LP containing no formal group. IR and NMR data show the formation of carbonyl-containing products by an oxidative free-radical pathway: 2D NMR data confirm that a formate ester is the main carbonyl-containing product, as authenticated recently in the degradation of various polyglycols. (C) 1998 Elsevier Science Limited. All rights reserved
To submit an update or takedown request for this paper, please submit an Update/Correction/Removal Request.