Abstract

In immiscible polymer blend nanocomposites, nanoparticles can be localised either in polymer matrices or at the interface, invoking the simple question of how the spatial distribution of the nanoparticles and the resulting morphological changes affect the non-isothermal crystallisation and degradation kinetics. In this study, the non-isothermal crystallisation of polypropylene in polypropylene (PP)-rich compatibilised and non-compatibilised PP/low-density polyethylene (LDPE)/clay composites and their degradation are investigated. The non-isothermal crystallisation analyses show that the localisation of the clay particles in the blend composites has two opposing effects. First, the poorly dispersed clay particles at the PP/LDPE interface in the non-compatibilised blend composite has no significant effect on the crystallisation temperature of PP but allows the free movement of PP chains, resulting in a higher crystallinity of PP than that of PP in the neat blend. Second, the well-dispersed clay particles in the compatibilised blend composites disrupt the free movement of PP chains, resulting in a lower crystallisation temperature and crystallinity than that of PP in the neat blend. The influences of different selective localisations of clay particles on the activation energies of degradation are studied. The presence of maleated compatibilisers, clay, and the distribution of clay in the blend composite play important roles in determining the activation energies of degradation.

Highlights

  • For many decades, polymer blends have attracted attention because the process of mixing two or more polymers with different physical properties provides a simple route for tailoring polymer properties for suitable applications

  • The higher energy of degradation (Ea) of the 80/20/5/5/4 nanocomposite is attributed to the complementary effects of the better compatibility between PP and low-density polyethylene (LDPE) promoted by incorporating PP-g-MA and PE-g-MA and the better distribution of nanoclay in all phases of the 80/20/5/5/4 composite

  • The present work investigated the effects of clay localisation and its distribution in an immiscible blend of PP/LDPE on the non-isothermal crystallisation and degradation kinetics

Read more

Summary

Introduction

Polymer blends have attracted attention because the process of mixing two or more polymers with different physical properties provides a simple route for tailoring polymer properties for suitable applications. The selective localisation of nanofillers in different polymeric phases of blend composites may influence the crystallisation and thermal degradation kinetics differently, and inadequate work has been carried out on this topic Given this background, we have previously melt-mixed clay containing PP/LDPE blend composites in the absence and presence of compatibilisers, PP-g-MA and maleated polyethylene (PE-g-MA), and investigated how the localisation of organically modified nanoclay particles affects the morphological development—and the properties—of the obtained composites [18]. From the viewpoint of fabricating ternary nanocomposites with tuneable properties, the main objective of this study is to investigate the influence of the localisation of clay particles in an (80/20) PP/LDPE blend and its resulting morphology on the non-isothermal crystallisation of PP and the kinetics of thermal degradation in the blend composite.

Materials
Sample Preparation
Characterisation Techniques
Melting and Cooling Properties
Non-Isothermal Crystallisation Kinetics
Calculation of the Activation Energy for Non-Isothermal Crystal Growth
Polarised Optical Microscopy
Thermal Degradation Kinetics
Conclusions
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call