The role of humidity in the photooxidation of acrylic melamine coatings

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Abstract

Predicting the weatherability of acrylic melamine coatings commonly used as enamel clearcoats requires a detailed understanding of each of the factors that influence photooxidation kinetics. Previous work1 has shown that the photooxidation rate in coatings can be written as the following function of hydroperoxide concentration: photooxidation rate = K[YOOH] + M. The existence of a measurable photooxidation rate in the absence of hydroperoxide (i.e. a non-zero value of the intercept, M) has been observed only in melamine crosslinked coatings. It has also been observed that the photooxidation rate in acrylic melamine coatings increases with increasing humidity. In contrast, for urethane crosslinked coatings the value of M is zero, and the photooxidation rate is independent of humidity. In this paper, infrared spectroscopic measurements of functional group changes (e.g. carbonyl growth and crosslink scission) are used to measure photooxidation rates in acrylic melamine coatings during UV exposures at different humidities. Comparisons of these rates to measured hydroperoxide concentrations for the same coatings and exposures reveal that the increase in photooxidation rate with humidity is due to the fact that the intercept M increases with increasing humidity. Since the intercept is zero under dry conditions, the chemical reactions responsible for the intercept in melamine crosslinked coatings must involve both UV light and moisture. These results confirm the importance of accurately controlling the humidity during UV exposure for predicting the weatherability of melamine crosslinked coatings.

References (16)

  • D.R. Bauer et al.

    Polym. Deg. Stab.

    (1992)
  • D.R. Bauer et al.

    Polym. Deg. Stab.

    (1990)
  • D.R. Bauer et al.

    Polym. Deg. Stab.

    (1990)
  • J.L. Gerlock et al.

    Polym. Deg. Stab.

    (1986)
  • J.L. Gerlock et al.

    Polym. Deg. Stab.

    (1986)
  • D.F. Mielewski et al.

    Polym. Deg. Stab.

    (1991)
  • D.R. Bauer et al.

    Polym. Deg. Stab.

    (1992)
  • D.R. Bauer et al.

    Polym. Deg. Stab.

    (1992)
There are more references available in the full text version of this article.

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