Abstract
AbstractN‐substituted maleimides have been investigated as thermal stabilizers for rigid polyvinylchloride (PVC) at 180°C in air by measuring the rate of dehydrochlorination and the extent of discoloration of the polymer. The results reveal the higher stabilizing efficiency of these products relative to basic lead carbonate, dibutyl tin maleate, and cadmium‐barium stearate stabilizers commonly used in industry. The induction period (Ts) increases as a function of the positive resonance effect of the substituents (+R). Moreover, the investigated stabilizers impart better color stability for the degraded samples as compared with the stearate stabilizer. The stabilizer efficiencies are attributed to their radical trapping potency which intervenes with the radical degradation process of PVC, while the good color stability is due to the ability of the stabilizer to interact with the conjugated double bonds formed on the PVC chains as a result of degradation. A mechanism illustrating the stabilizer's action is proposed.
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