The absorption and desorption of chlorobenzene, o-dichlorobenzene, and
chloroform in poly[n-butyl methacrylate] (PBMA) was studied in polyme
r-coated 104 MHz surface acoustic wave (SAW) sensors, and in freestand
ing polymer films by thermogravimetric analysis (TGA). The sorption pr
ocesses were analyzed by a Fickian simulation and best-fit partition,
and diffusion coefficients were derived. Good correlations were found
between simulated and observed data. Partition coefficients derived fr
om SAW response were independent of coating thickness and were found t
o be about two to three times bigger than those derived from the gravi
metric response, In contrast,, the diffusion coefficients increased li
nearly with csa ting thickness in the range 70-560 kHz. For the thicke
st polymer coating, SAW-derived diffusion coefficients were comparable
with TGA-related diffusion coefficients. This study reconfirms the fi
nding for other polymers that the response of SAW chemosensors is high
er than that anticipated from a mass change. only. The viscoelastic ef
fect is again more pronounced than the gravimetric effect, Moreover, t
he similarity of diffusion coefficients obtained at higher polymer thi
cknesses suggests that the rate of change of the SAW viscoelastic comp
onent is similar to that of the gravimetric element. It is fair to ass
ume that both processes originate from the same event: the absorption
of the analyte in the polymer, In this view the polymer-coated SAW sen
sor may be regarded as an enhanced gravimetric sensor.