Article
Synthesis of Chain-End Functionalized PP and Applications in Exfoliated PP/Clay Nanocomposites
Article first published online: 2 JUN 2005
DOI: 10.1002/masy.200550710
Copyright © 2005 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Issue
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Macromolecular Symposia
Special Issue: Polymers in Novel Applications
Volume 225, Issue 1, pages 113–128, May 2005
Additional Information
How to Cite
Wang, Z.M., Han, H. and Chung, T.C. (2005), Synthesis of Chain-End Functionalized PP and Applications in Exfoliated PP/Clay Nanocomposites. Macromol. Symp., 225: 113–128. doi: 10.1002/masy.200550710
Publication History
- Issue published online: 2 JUN 2005
- Article first published online: 2 JUN 2005
- Abstract
- Cited By
Keywords:
- functionalization;
- metallocene;
- nanocomposite;
- polypropylene;
- PP/clay composite
Abstract
This paper summarizes our research to the preparation of chain-end functionalized isotactic polypropylene (i-PP) having a terminal functional group, such as an OH and an NH2. The chemistry involves metallocene-mediated propylene polymerization using the rac-Me2Si[2-Me-4-Ph(Ind)]2ZrCl2/MAO complex in the presence of styrene derivatives (St-f) and hydrogen, which serve as the chain transfer agents. The molecular weight of the resulting i-PP polymers with terminal OH or NH2 groups (i.e., PP-t-OH and PP-t-NH2) are inversely proportional to the molar ratio of [St-f]/[propylene]. Despite the extremely low concentration of functional groups, the high molecular weight NH3+-terminated PP (PP-t-NH3+) exhibits a distinctive advantage over other functional PP polymers containing side chain functional groups or long functional blocks. The terminal hydrophilic NH3+ cation, with good mobility and reactivity, effectively ion-exchanges the cations (Li+, Na+, etc.) located between the clay interlayers, and anchors the PP chain to the clay surfaces. On the other hand, the remaining rest of the unperturbed, end-tethered, high molecular weight PP tail exfoliates the clay layers. This exfoliated structure is maintained even after further mixing of the PP-bearing platelets with pure, neat PP polymers.

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