The effects of addition of a reactive compatibilizer, a random terpolymer,
on morphological and rheological properties of blends of polyamide disperse
d in a polyethylene matrix were studied experimentally. This addition leads
to smaller size and narrower size distribution of the dispersed phase. Thi
s has been related to the presence, at the interface, of copolymers, formed
in situ by reaction between the polyamide and the terpolymer, which form a
n interphase between the nodules and the matrix. The linear viscoelasticity
of these compatibilized blends reveals that, in addition to the form relax
ation process (relaxation time lambda (d)) even observed in absence of comp
atibilizer, another relaxation process, which has been related to the dynam
ics of nodule-matrix interphase, is observed at a characteristic time lambd
a (int) higher than lambda (d). The concentration and molecular weight depe
ndence of this characteristic time lambda (int) and the intensity H-int of
the relaxation mechanism associated to lambda (int) has been investigated.
The steady shear measurements exhibit an unusual behavior never observed be
fore in blends of immiscible polymers. Indeed, the viscosity curve shows tw
o plateau regions, respectively, at low and moderate shear rates, connected
by a rather steep portion of curve, which is associated to a characteristi
c time of the same order of magnitude as lambda (int). This behavior has be
en interpreted by considering that the response of the system at the lowest
shear races is dominated by the molecular dynamics of the nodule-matrix in
terphase, whereas at higher shear rates the system behaves as an emulsion w
ith hydrodynamic particle-particle interactions. The viscosity excess, due
to the slowest relaxation process and expressed as the difference between t
he two plateau viscosities, shows a marked dependence on both concentration
and molecular weight of the compatibilizer. (C) 2000 The Society of Rheolo
gy. [S0148-6055(00)01005-1].