Abstract

The labile hydrogen of the carbamate group is primarily responsible for color development in the thermal degradation of polyurethane. Replacement of this hydrogen by an alkyl group prevents back-dissociation. Accordingly, a number of N-substituted polyurethanes were prepared, including the methyl, benzyl, benzoyl, acetyl, and the (N-phenylamido) derivatives. Comparative studies at 150–155°C. showed that the N-methyl and N-benzyl polymers possess outstanding stability under the condition of our testing.

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