X-ray-induced damage in Estane(R)5703 has been studied by luminescence, opt
ical absorption and electron spin resonance techniques in the temperature i
nterval approximate to 10-300 K. Molecular motion of the polymer soft segme
nt, as determined by viscoelastic measurements, is correlated with features
in the glow curve, indicating charge detrapping via thermal destruction of
cavity traps. Spectral emission is characterized by four Lorentzian bands
with maxima at 2.38, 2.55, 2.74 and 2.93 eV, which are attributed to triple
t-to-singlet (pi, pi*) electronic transitions of the phenyl group in the po
lymer hard segment. Absorption peaks at 3.97, 4.29 and 4.46 eV are also ass
igned to transitions within this group. Several radicals with overlapping r
esonances are induced at 35 K, which, with increasing temperature, evolve i
nto the relatively stable peroxy free-radical at room temperature. (C) 1999
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