The main concepts of the existing kinetic models, describing the oxida
tion of partly crystalline polyolefins, are critically analyzed, These
models are based on the schemes of homogeneous liquid-phase processes
and the Gugumus notions of a combination of homogeneous and heterogen
eous mechanisms in the initiation of oxidation of the amorphous polyme
r domains. The most significant discrepancies between the existing mod
els and experimental facts reported in the literature are considered,
A structural-kinetic model of the oxidation process is described, whic
h takes into account a microheterogeneous structure of the amorphous d
omains and allows the chain oxidation kinetics of these domains in bot
h solid and melted polymers Id be interpreted on the common grounds.