Blends of isotactic Polypropylene (iPP) and Oligo Cycle Pentadiene (HOCP) w
ere studied both from a structural (SAXS and SANS) and dynamical (Raman sca
ttering) point of view. In the solid state these blends present a lamellar
morphology, crystalline iPP layers alternating to amorphous iPP+HOCP layers
. The blend phase diagram is characterized by the existence of a miscibilit
y gap. SAXS and SANS techniques are applied to investigate the structural.
features of both in-gap and out-of-gap blends. SAXS and SANS patterns were
Fourier inverted in order to extract the self-correlation fuction of the el
ectronic (scattering length) density gamma(x). gamma(x)'s were analysed in
terms of a pseudo two-phase model, in the case of out-of-gap blends. This m
odel allows to derive structural parameters, such as crystalline, amorphous
and total(long period) thicknesses. As far as the dynamical response is co
ncerned, low-frequency depolarized light scattering measurements on iPP, Po
lyethylene (PE) and their blends with HOCP, at melting point, were performe
d. This experimental dynamical study has the goal to show the main role pla
yed by the effective vibrational density of states in comparison with the r
eorientational diffusion contribution, since relaxations and vibrations are
the two main terms that contribute to low-frequency Raman spectra of glass
formers. On the other hand, the existence of a boson peak, characteristic
of glass-forming systems, whose center-frequency shifts towards higher valu
es, increasing the percentage of HOCP, indicates the disorder effect connec
ted to the presence of this component in the polymer ic blends, as also sho
wn by the evolution of the dynamical correlation length, R-c. Furthermore i
n the very low frequency range a crossover (omega(CO) similar to 0.1 THz) f
rom a spectral phonon-like contribution to a fracton-like is detected. This
behaviour has been interpreted accordingly with the recent theories on the
excess of spectral density in such a kind of systems.