Molecular composites made of ionic poly(p-phenylene terephthalamide) and poly(4-vinylpyridine): Relaxation behavior

Molecular composites were prepared from several types of ionically modified, poly(p‐phenylene terephthalamide) (PPTA) dispersed in a poly(4‐vinylpyridine) matrix. Optical clarity tests indicated that the component polymers of the composite were miscible, at least at low concentrations of the rodlike...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of polymer science. Part B, Polymer physics Polymer physics, 2002-06, Vol.40 (11), p.1110-1117
Hauptverfasser: Chen, W. C., Sauer, J. A., Hara, M.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Molecular composites were prepared from several types of ionically modified, poly(p‐phenylene terephthalamide) (PPTA) dispersed in a poly(4‐vinylpyridine) matrix. Optical clarity tests indicated that the component polymers of the composite were miscible, at least at low concentrations of the rodlike reinforcement. In composites containing ionic PPTA, where ionic sulfonate groups were attached as side groups either to PPTA chains or to PPTA anion chains, the glass‐transition temperature (Tg) was increased by l0 °C or more, at 5 wt % reinforcement. At concentrations of 10–15 wt % of the ionic polymer, Tg values leveled off or decreased slightly. This suggested that some aggregation of the rigid‐rod molecules occurred. In composites containing ionic PPTA, where the ionic sulfonate groups were directly attached to the phenylene rings of PPTA chains, not only was Tg shifted significantly to higher temperatures, but the rubbery plateau modulus retained high values up to temperatures of 250 °C or above. Observed effects were considered to be the result of strong ionic interactions between the ionic reinforcement polymer and the polar matrix polymer. The possible effects of the counterion on Tg and the storage modulus are discussed. © 2002 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 40: 1110–1117, 2002
ISSN:0887-6266
1099-0488
DOI:10.1002/polb.10169