Natural and artificial weathering characteristics of stabilized acrylic–urethane paints

Abstract

Depth-profiling by Fourier transform infrared (FTIR) spectroscopy, dynamic mechanical analysis (DMA), microhardness and scanning electron microscopy (SEM) observations have been used to monitor degradation chemistries in two-package acrylic–urethane coatings when exposed to different exposure conditions. Three artificial and three natural weathering protocols (QUV, ASTM D5894, ISO20340, Pipady (south of France), Bandol (south of France) and Kure Beach (USA)) were selected for this study. The same chemical events were found to occur under all conditions, particularly under natural and artificial exposures. Both loss of the amide II band at 1520 cm −1 and carbonyl growth occurred but at relatively low rate owing to the presence of hindered-amine light stabilizers in the film. A less typical loss of urea biuret linkages also occurs during all exposures and results in a change in the balance between urethane and urea links across the depth of the film during weathering. The chemical degradation of the polymer matrix involves the formation of species that are readily ablated from the surface and results in loss of gloss, increase in hardness and a rougher topology. The dramatic loss of gloss observed after Pipady and Bandol exposures show that loss of gloss should not be systematically correlated to the advance in chemical degradation.