It was shown that when polyurethanes designed for use in biopolymer ap
plications were immersed in orienting fluids, significant increases in
their non-dispersive surface energies took place. The kinetics of the
surface energy response were found to be a function of the immersion
medium's acid-base interaction potential. Restructuring from the as-ca
st state, similar to that reported for two-component polyurethane adhe
sives, occurs in response to thermodynamic demands and is attributable
to a preferential concentration of low energy segments in the surface
region. Since shifting surface energies in polyurethanes may pose pro
blems in biological applications, an attempt was made to crosslink the
surface of the polymers by the use of cold, microwave plasma discharg
es with Argon as the treatment gas. Plasma treatments proved to be suc
cessful, in that polyurethane surfaces so modified responded much more
weakly to changes in the polarity of contact media.