Issue 20, 2014

Suppression of phase coarsening in immiscible, co-continuous polymer blends under high temperature quiescent annealing

Abstract

The properties of polymer blends greatly depend on the morphologies formed during processing, and the thermodynamic non-equilibrium nature of most polymer blends makes it important to maintain the morphology stability to ensure the performance stability of structural materials. Herein, the phase coarsening of co-continuous, immiscible polyamide 6 (PA6)–acrylonitrile-butadiene-styrene (ABS) blends in the melt state was studied and the effect of introduction of nano-silica particles on the stability of the phase morphology was examined. It was found that the PA6–ABS (50/50 w) blend maintained the co-continuous morphology but coarsened severely upon annealing at 230 °C. The coarsening process could be divided into two stages: a fast coarsening process at the initial stage of annealing and a second coarsening process with a relatively slow coarsening rate later. The reduction of the coarsening rate can be explained from the reduction of the global curvature of the interface. With the introduction of nano-silica, the composites also showed two stages of coarsening. However, the coarsening rate was significantly decreased and the phase morphology was stabilized. Rheological measurements indicated that a particle network structure was formed when the concentration of nano-silica particles was beyond 2 wt%. The particle network inhibited the movement of molecular chains and thus suppressed the coarsening process.

Graphical abstract: Suppression of phase coarsening in immiscible, co-continuous polymer blends under high temperature quiescent annealing

Article information

Article type
Paper
Submitted
29 Dec 2013
Accepted
11 Feb 2014
First published
11 Feb 2014

Soft Matter, 2014,10, 3587-3596

Suppression of phase coarsening in immiscible, co-continuous polymer blends under high temperature quiescent annealing

X. Liu, R. Li, R. Bao, W. Jiang, W. Yang, B. Xie and M. Yang, Soft Matter, 2014, 10, 3587 DOI: 10.1039/C3SM53211A

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