The influence of phase morphology and carbon black distribution on energy s
torage and dissipation during dynamic excitations of rubber blends is discu
ssed. It is shown that differences in the local stiffness of the phases in
the glass transition regime of unfilled blends lead to characteristic devia
tions of the local strain from the external strain amplitude. These deviati
ons are governed by a critical phenomenon due to the formation of a phase n
etwork above a critical blend ratio. As a result, a strongly nonlinear depe
ndence of the glass transition maxima of the loss modulus on the volume fra
ction of the phases is observed. By counting the elastically effective bond
s of the phase network, the local strain amplitude is estimated by purely g
eometrical arguments. Based on a consideration of the phase network, the di
stribution of carbon black in the different phases of filled blends is esti
mated from the height of the local maxima of the loss modulus in the glass
transition regime. Thereby, a linear increase of the maximum value of the l
oss modulus with rising carbon black concentration is exploited that relate
s the enhanced energy dissipation of filled rubbers to the internal frictio
n of the filler particles. Results on EPDM/BR/N550 blends indicate that car
bon black is preferably located in the BR phase. A somewhat higher concentr
ation of carbon black in the SBR phase is found in the case of NR/SBR(40% S
tyrene)/N330 blends.