Forced Rayleigh scattering (FRS) has been used to measure the tracer d
iffusion coefficient of azobenzene in low molecular weight polystyrene
(PS) as a function of temperature, and in high molecular weight PS pl
asticized by CO2 at 35 degrees C and CO2 pressures from 14 to 85 bar.
In contrast to dye diffusion in pure PS and PS plasticized by tricresy
l phosphate, where the effect of plasticization by temperature, chain
ends, or added diluent can be accounted for by (T - T-g) scaling, dye
diffusion in CO2-plasticized PS is enhanced by 2-3 orders of magnitude
over values predicted on the basis of T-g depression alone. This enha
ncement begins at surprisingly low CO2 pressures (<15 bar at 35 degree
s C) and is maintained across the CO2-induced glass transition. A larg
e difference in mobilities of the cis and trans isomers of azobenzene
is also observed in the presence of CO2, which is much greater than th
at seen in the experiments on pure PS. Two additional FRS relaxation m
odes unrelated to translational diffusion of the dye molecules have be
en identified in this study: a fast, local relaxation attributed to dy
e rotation, and a slow relaxation attributed to the dynamic response o
f the PS/CO2 matrix to a chemical potential driving force associated w
ith the azobenzene isomers.