The penetration of aqueous solutions at different pH values into pristine a
nd ion-irradiated commercial polyimide (PI, "Kapton") foils was examined, b
y using Li ions as tracers to probe the corresponding penetrant depth distr
ibutions. These distributions were recorded for different polymer exposure
times and temperatures. For comparison, examinations have also been made on
the time dependence of the polyimide conductivity during water uptake. The
results derived here for PI are compared with those of other polymers.
For both pristine and low-fluence irradiated PI, an initially rapid solutio
n penetration was observed up to some maximum penetrant uptake value. The p
enetrant depth distributions point at nanocapillaric penetration mechanisms
in this initial stage. At longer exposure times of the polymer, the penetr
ant concentration diminishes transiently, suggesting that polymer swelling
in the confined track zone leads to a reduction of the available free volum
e. In the subsequent stage of penetrant uptake this process is reversed aga
in which we explain by crazing and overall swelling. Whereas thereafter sat
uration is reached for non-alkaline penetrants, alkaline solutions in irrad
iated PI show a pronounced continuous uptake, which is correlated with the
ion track etching process.
Whereas low-fluence ion irradiation of PI leads to a reduction in penetrant
uptake compared with the pristine material, high-fluence irradiation resul
ts in a pronounced increase of the uptake capability. (C) 1999 Elsevier Sci
ence Ltd. All rights reserved.