Reactive coupling between immiscible polymer chains: Acceleration by compressive flow

Jie Song, Adam M. Baker, Christopher W. Macosko, Randy H. Ewoldt

Research output: Contribution to journalArticlepeer-review

Abstract

It is demonstrated that processing flow affects the kinetics of the interfacial coupling reaction between functional groups that are grafted to polymer chains. At melt temperatures the amine group on the end of nylon 6 chains reacts with maleic anhydride grafted polyethylene (PE-MA) and forms graft copolymers. Bilayers were made by lamination and coextrusion and adhesion was measured using asymmetric dual cantilever beam (ADCB). The amount of graft copolymer in the interface was quantified by X-ray photon spectroscopy (XPS). With quiescent lamination, adhesion increased with temperature and the concentration of PE-MA. The adhesion metric, Gc (critical energy release rate), plotted as a function of Σ (interfacial copolymer density) fell on the same master curve, unifying reaction process, temperature and time. Gc was a linear function of Σ for low-copolymer coverage and weak adhesion. For relatively high coverage and strong adhesion, Gc scaled with Σ. Coextrusion with compressive flow resulted in a reaction rate strikingly two-orders of magnitude faster than that without compressive flow. The rate in the noncompressive die was close to quiescent lamination. Even for lamination, when compressive flow was applied normal to the interface, the coupling reaction rate was also greatly accelerated. Several mechanisms are speculated for this remarkable acceleration in polymer chain coupling.

Original languageEnglish (US)
Pages (from-to)3391-3402
Number of pages12
JournalAIChE Journal
Volume59
Issue number9
DOIs
StatePublished - Sep 2013

Keywords

  • Interfacial processes
  • Multiphase flow
  • Polymer processing
  • Reaction kinetics
  • Rheology

ASJC Scopus subject areas

  • Biotechnology
  • Environmental Engineering
  • General Chemical Engineering

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