A. Schmoldt et al., IRRADIATION OF PMMA WITH HIGH-ENERGY LIGHT-IONS - THE DEPTH DISTRIBUTION FOR VOLATILE REACTION-PRODUCT EMISSION, Radiation effects and defects in solids, 128(4), 1994, pp. 277-285
Mass spectrometry has been used as an analytical tool in determining t
he species and quantities of volatile reaction products generated duri
ng destruction of polymers by ion implantation. Specifically, one very
important objective was to relate the radiation chemistry with the ra
diation physics of fundamental track formation. Experiments are descri
bed in which the depth distribution of the emission of volatile produc
ts has been determined for irradiation of PMMA with 35MeV Li-7(2+) ion
s. The mass spectral measurements of the reaction products were carrie
d out on thin PMMA foils as a function of the angle of beam incidence,
and hence of penetration depth. Correlation of the differences in mas
s spectra with the foil number yielded the depth distribution of degas
sing. Comparison with theory shows that volatile gas degassing, which
is itself a consequence of multiple chain scission, can be related to
electronic rather than nuclear energy transfer processes. However, the
detailed shape of the measured degassing distribution differs from th
at expected from theory. This clearly points to inherent inadequacies
in the simple model for polymer destruction.