Concurrent physical aging and degradation of crosslinked coating systems in accelerated weathering

Coating degradation is a combination of both chemical and physical processes; however, physical processes have not received much attention. Physical aging has a non-negligible effect on coatings’ mechanical properties and permeability etc. through the densification that continues as a polymer approaches its thermodynamic equilibrium below the glass transition temperature, T _g. Observations in recent work showed that physical aging affects coatings’ mechanical property response during accelerated weathering and is, itself, affected by the associated chemical degradation. Two crosslinked coating systems were studied in order to compare different chemical compositions, their T _g, and their thermal response in accelerated weathering. During thermal cycling, physical aging measured by enthalpy recovery exhibited different trends in the two coatings. A “rejuvenation” mechanism was observed in the coating with a T _g between the top and bottom limits of the exposure cycle; continued aging was observed for the coating with a high T _g. Stress relaxation tests detected aging and “memory” behavior over periods comparable with accelerated weathering cycles. Both thermal and mechanical responses changed in complicated and different ways as the coatings degraded. Different degrees of coating thickness reduction were observed in both isothermal relaxation and degradation. When various coatings are evaluated, simply judging their performance under the same weathering environment is not reliable since polymer relaxation behavior depends on the relationship between the exposure temperatures and the T _g of each polymer.