The physical and mechanical properties of beta-nucleated polypropylene/montmorillonite nanocomposites
Article first published online: 20 MAY 2011
Copyright © 2011 Wiley Periodicals, Inc.
Journal of Applied Polymer Science
Volume 122, Issue 2, pages 1066–1076, 15 October 2011
How to Cite
Prachum, Y., Adam Strauss, R. H. and Kiatkamjornwong, S. (2011), The physical and mechanical properties of beta-nucleated polypropylene/montmorillonite nanocomposites. J. Appl. Polym. Sci., 122: 1066–1076. doi: 10.1002/app.34209
- Issue published online: 5 JUL 2011
- Article first published online: 20 MAY 2011
- Manuscript Accepted: 25 JAN 2011
- Manuscript Received: 18 NOV 2010
Polypropylene (PP) and polypropylene/polypropylene-g-maleic anhydride/ organomontmorillonite (PP/PP-g-MA/OMMT) nanocomposites were modified with 0.05 to 0.3% (w/w) of the aryl amide β-nucleator to promote the formation of hexagonal crystal modification (β-phase) during melt crystallization. The nonisothermal crystallization behavior of PP, PP/PP-g-MA/OMMT and β-nucleated PP/PP-g-MA/OMMT nanocomposites were studied by means of differential scanning calorimetry. Structure-property relationships of the PP nanocomposites prepared by melt compounding were mainly focused on the effect and quantity of the aryl amide nucleator. The morphological observations, obtained from scanning electron microscopy, transmission electron microscopy and X-ray diffraction analyses are presented in conjunction with the thermal, rheological, and mechanical properties of these nanocomposites. Chemical interactions in the nanocomposites were observed by FT-IR. It was found that the β-crystal modification affected the thermal and mechanical properties of PP and PP/PP-g-MA/OMMT nanocomposites, while the PP/PP-g-MA/OMMT nanocomposites of the study gained both a higher impact strength (50%) and flexural modulus (30%) compared to that of the neat PP. β-nucleation of the PP/PP-g-MA/OMMT nanocomposites provided a slight reduction in density and some 207% improvement in the very low tensile elongation at break at 92% beta nucleation. The crystallization peak temperature (Tcp) of the PP/PP-g-MA/OMMT nanocomposite was slightly higher (116°C) than the neat PP (113°C), whereas the β-nucleation increased the crystallization temperature of the PP/PP-g-MA/OMMT/aryl amide to 128°C, which is of great advantage in a commercial-scale mold processing of the nanocomposites with the resulting lower cycle times. The beta nucleation of PP nanocomposites can thus be optimized to obtain a better balance between thermal and mechanical properties. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011.