Abstract
AbstractThe thermal decomposition of Thioped, a liquid polysulfide polymer based on dichloroethyl formal, was studied using pyrolysis–GC–MS. The nature and composition of the products of pyrolysis at 358 and 485°C are given. A striking feature of the product analysis is the presence of several disulfide compounds only at the higher decomposition temperature. The pyrolysis‐GC of other liquid polysulfide polymers (LP‐2, LP‐32, LP‐3, and LP‐33) showed that molecular weight had only marginal effect on the product composition. Ionic and radical mechanisms were considered to account for the product formation. Isothermal and dynamic thermogravimetric studies were carried out to differentiate between the two mechanisms. The results were found to be in agreement with a free radical mechanism, with cleavage of the formal CO linkage as the preferred mode of initiation. The overall activation energy for the decomposition was found to be 190 kJ mol−1.
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