The polymer/polymer interdiffusion in a binary compressible blend consistin
g of long and short chains is investigated within the framework of the dyna
mic random phase approximation (RPA). The relative contributions of two (fa
st and slow) stages into the total relaxation of compositional heterogeneit
ies are explicitly shown to be strongly dependent on the initial conditions
and the degree of asymmetry of the blend. Special emphasis is given to the
influence of the initial distribution of free volume on the apparent rate
of the composition relaxation. The evolution of the dynamic struture factor
is described as well. It is shown that most of the peculiarities usually a
scribed to the "fast-mode" behavior can be derived within the RPA approach.