P. Gijsman et al., Comparison of the UV-degradation chemistry of polypropylene, polyethylene,polyamide 6 and polybutylene terephthalate, POLYM DEGR, 65(3), 1999, pp. 433-441
The photodegradation mechanism of polymers highly depends on the type and c
oncentration of chromophores present. This influence is studied by making a
comparison between the UV-degradation of PE, PP, PA6 and PET and the therm
ooxidative degradation of Pf at a comparable temperature. The degradation p
rocesses are followed by determining the oxygen uptake, CO, CO2 and peroxid
e formation. During UV-degradation of PP, PE, PA6 and PET the oxygen uptake
is linear in time without an induction period. The oxidation rate of PP is
higher than that of PET, which is slightly higher than the oxidation rate
of PA6, while that of PE is the lowest. The determined amount of peroxides
depends on the ageing time. For the UV-degradation this does not lead to th
e expected increase of the oxidation rate, as is the case with thermooxidat
ion of PP. Only a limited proportion of the peroxides formed during the UV-
degradation decomposes into radicals. The oxidation rate is mainly determin
ed by other radical forming reactions. In the case of PE and PP this is pro
bably initiation by polymer-oxygen Charge Transfer Complexes (CTCs) and for
PA6 and PET direct photolysis of the amide or the ester linkage, respectiv
ely. Thickness degradation profiles show that the UV-degradation processes
of PP and PET are heterogeneous. For PP this is due to oxygen diffusion lim
itation, while in the case of PET it is the result of absorption of the UV-
light. (C) 1999 Elsevier Science Ltd. All rights reserved.