The surface modification of poly(ethylene terephthalate) (PET) and UV-cured
tripropyleneelycol diacrylate (acrylic) films induced by remote N-2 and Ar
microwave plasmas (2.45 GHz) was compared by in-situ! XPS measurements. Bo
th N-2 and Ar plasma treatments led to destruction of the initial oxygen-co
ntaining groups. The destruction of ester groups was much faster fur the ac
rylic than for the PET film, and the destruction of ether groups was much f
aster than that of ester groups within the acrylic Blm. Among the plasma Ea
ses, N-2 was more effective than Ar in the cast: of PET, but their differen
ce was negligible in the case of the acrylic film. The higher stability of
thc PET surface was attributed to the presence of a rigid aromatic backbone
, which protected the ester groups from plasma UV irradiation and stabilize
d the free radicals. The lower stability of the acrylic film was associated
with the presence of weak ether groups. New functional groups were created
, attributed to carbonyl in the case of Ar, and carbonyl/amide and amine in
the case of N-2 plasma treatments. The Formation of these new Functional g
roups was very small compared with the loss of ether and eater groups, sugg
esting that the destruction of these oxygen-containing groups proceeded mai
nly through elimination of the entire groups.