The absorption and desorption of chlorobenzene, odichlorobenzene, and chloroform in poly[n-butyl methacrylate] (PBMA) was studied in polymer-coated 104 MHz surface acoustic wave (SAW) sensors, and in freestanding polymer films by thermogravimetric analysis (TGA). The sorption processes 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 from SAW response were independent of coating thickness and were found to be about two to three times bigger than those derived from the gravimetric response. In contrast, the diffusion coefficients increased linearly with coating thickness in the range 70-560 kHz. For the thickest polymer coating, SAW-derived diffusion coefficients were comparable with TGA-related diffusion coefficients. This study reconfirms the finding for other polymers that the response of SAW chemosensors is higher than that anticipated from a mass change only. The viscoelastic effect is again more pronounced than the gravimetric effect. Moreover, the similarity of diffusion coefficients obtained at higher polymer thicknesses suggests that the rate of change of the SAW viscoelastic component is similar to that of the gravimetric element. It is fair to assume that both processes originate from the same event: the absorption of the analyte in the polymer. In this view the polymer-coated SAW sensor may be regarded as an enhanced gravimetric sensor.