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Macromolecular modifications of poly(etherketoneketone) (PEKK) copolymer at the melting state

Article dans une revue avec comité de lecture
Author
CHOUPIN, Tanguy
244009 Airbus Group Innovations [Suresnes]
BRULE, Benoît
238410 Arkema
333368 Delft University of Technology [TU Delft]
CINQUIN, Jacques
244009 Airbus Group Innovations [Suresnes]
ccREGNIER, Gilles
86289 Laboratoire Procédés et Ingénierie en Mécanique et Matériaux [PIMM]
ccFAYOLLE, Bruno

URI
http://hdl.handle.net/10985/13818
DOI
10.1016/j.polymdegradstab.2018.07.005
Date
2018
Journal
Polymer Degradation and Stability

Abstract

Macromolecular modifications of poly(etherketoneketone) (PEKK) copolymer prepared from diphenyl ether (DPE), terephthalic acid (T) and isophthalic acid (I) with a T/I ratio of 60/40 have been investigated above its melting temperature by gel permeation chromatography (GPC), differential scanning calorimetry (DSC) and rheological measurements to assess the evolution of PEKK matrix during composite consolidation step. We mainly focused in this study on anaerobic conditions, i.e. degradation under nitrogen or in lack of oxygen. During exposure, thermal degradation leads to an increase of weight average molar mass Mw and viscosity which is typical to crosslinking/branching mechanism as already observed for PEEK in the literature. However, thanks to GPC measurements, it appears that a chain scission mechanism occurs in the same time related to a constant number average molar mass Mn. Crosslinking kinetics are identified at several temperatures between 320 and 400 °C with rheological measurements from a kinetic scheme governing the crosslinking mechanism. At last, the influence of the crosslinking process on PEKK crystallization is investigated. The final crystallinity and crystallization kinetics decrease with crosslinking due to branching of macromolecular chains.

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