Abstract

Abstract The thermal stability and structural details were compared for fractions of S-PVC and a series of “U-PVC” prepared at sub-saturation conditions. Molecular weights and long chain branching were obtained by GPC and viscometry. “Labile chlorine” was determined by phenolysis, double bonds by bromination, and endgroup structure by NMR. The rate of thermal dehydrochlorination was determined in nitrogen at 190°C. In S-PVC there are few tertiary chlorine, and phenolysis therefore measures allylic chlorine. By NMR it was found that ∼CH2-CH[dbnd]CH[sbnd]CH2Cl is the main unsaturated structure. Phenolysis and bromination therefore mainly give a measure of this group. The main saturated chain end is ∼CHCl[sbnd]CH2Cl. These groups account for 80% of the endgoups and are the result of the mechanism of chain transfer to monomer: head-to-head addition followed by 1,2-Cl migration and Cl· elimination. They have only a weak influence on the thermal stability, however. U-PVC, on the other hand, shows a strong relat...

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