Modulated differential scanning calorimetry was used to probe the thermal behavior of poly(methyl methacrylate) (PMMA) adsorbed onto silica from solution and subsequently dried. Changes in the glass transition were studied as a function of the adsorbed amount and solvent system used to deposit the polymer. The glass transition temperature (T-g) of PMMA was found to increase from 108 degrees C for the bulk polymer to 136 degrees C for the polymer adsorbed on silica from toluene (1.0A(m)). For the polymer adsorbed at approximately half that amount (0.6A(m)), the glass transition temperature increased to 158 degrees C. The breadth of the transition also increased from 11 degrees C for bulk to 61 and 58 degrees C for the 1.0A(m) and 0.64(m) samples, respectively. When PMMA was adsorbed from a mixed solvent system (5:1 benzene/acetonitrile solution), the transition temperature and its breadth increased even further. For a sample with 0.5A(m) adsorbed amount from the mixed solvent system, the T-g was increased to 167 degrees C and the width of the transition was increased to 65 degrees C. The change in thermal behavior was attributed to polymer chain confinement, resulting in a distribution of segmental mobilities different from that of the bulk polymer. Upon aging for 328 days from the original analysis date, the polymer chains in the 0.6A(m) sample adsorbed from toluene rearranged, resulting in thermal behavior which was more like that of the 0.5A(m) sample adsorbed from the mixed solvent system.