Highly linear or
high-density polyethylenes (HDPEs) have an intrinsically
high nucleation density compared to other polyolefins. Enhancing their
nucleation density by self-nucleation is therefore difficult, leading
to a narrow self-nucleation
Domain
(i.e., the so-called
Domain
II
or the temperature
Domain
where self-nuclei can be injected into the material without the
occurrence of annealing). In this work, we report that when HDPE is
blended (up to 50%) with immiscible matrices, such as atactic polystyrene
(PS) or Nylon 6, its self-nucleation capacity can be greatly increased.
In addition, temperatures higher than the equilibrium melting temperature
of the HDPE phase are needed to erase the significantly enhanced crystalline
memory in the blends. Morphological evidence gathered by Scanning
and Transmission Electron Microscopies (SEM and TEM) indicates that
these unexpected results can be explained by the modification of the
interface between blend components. The filling of the solid HDPE
surface asperities by the low viscosity polystyrene during heating
to the self-nucleation temperature, or the crystallization of the
matrix in the case of Nylon 6, enhances the interface roughness between
the two polymers in the blends. Such rougher interfaces can remarkably
increase the self-nucleation capacity of the HDPE phase via surface
nucleation.