Coarse-grained molecular dynamics simulations for oxidative aging of polymers under various O2 concentrations

T Ishida and K Haremaki and Y Koide and T Uneyama and Y Masubuchi, POLYMER DEGRADATION AND STABILITY, 239, 111404 (2025).

DOI: 10.1016/j.polymdegradstab.2025.111404

Modeling of polymer oxidative aging has been actively studied since the 1990s. Insights from these studies suggest that the transport of oxygen and radicals significantly influences aging heterogeneity, alongside chemical reaction kinetics. A recent simulation study Ishida et al., Macromolecules, 56(21), 8474-8483, 2023 demonstrated that mesoscale heterogeneity arises when the H-abstraction reaction occurs faster than the relaxation times of polymer chains. In this study, the simulations were extended by modeling the rate of oxygen addition to polymer radicals (k2) to reflect the effects of the O2 concentration. In this work, polypropylene was chosen as a representative example of the target polymer. Three key aspects of oxidative aging behavior were found to be influenced by the O2 addition rate: (i) reaction kinetics, (ii) the degree of heterogeneity, and (iii) amount of crosslinking. Namely, reducing O2 concentration slows the conversion of polymer radicals into H-abstractable peroxyl radicals. This deceleration delays H-abstraction reactions, increases the number of polymer radicals, and promotes crosslinking reactions between two polymer radicals.

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