ABSTRACT:The mechanical, thermal, and gas permeation properties of polypropylene (PP)/oligopinene systems in the form of compression thin films 10 m thick, which were prepared by quenching (with liquid nitrogen) and slow-cooling (15°C/min) techniques, were examined. The addition of oligopinene to PP changed the stress-strain curve of the polyolefin. Both for quenching and slow-cooling films, with a higher oligomer content, no more yielding was observed, and the elongation at break abruptly decreased with greater than 10% oligomer. The elastic modulus and stress at break changed according to the thermal conditions of the film preparation. Thermal analysis revealed that the blend system had two glass-transition temperatures for both types of films. The values of permeation to CO 2 were independent of the film preparation and were practically unchangeable with the oligomer content in the blends, indicating that the overall decrease in the crystallinity was counterbalanced by the rigidity of the two amorphous phases.