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Solid StateCross-Linked Polypropylene via ReactiveExtrusion: A Scalable Approach

  • Jonas J. Perez-Bravo*
  • , Javier Gonzalez-Benito
  • , Jules A. W. Harings
  • *Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Solid-state reactive extrusion provides a promising route for modifying semicrystalline polymers while minimizing degradation associated with conventional melt processing. Here, isotactic polypropylene was modified using benzoyl peroxide at 110 °C, below the polymer melting temperature. Under these conditions, radical reactions occur within the amorphous regions of the semicrystalline matrix while crystalline lamellae remain intact and restrict large-scale chain motion. FTIR and 13C CP-MAS NMR analyses indicate that the polypropylene backbone is largely preserved after processing. Differential scanning calorimetry shows increased crystallization temperatures and reduced crystallinity, consistent with restricted chain mobility and network-induced nucleation. Rheological measurements reveal a progressive increase in the storage modulus with increasing peroxide concentration and a transition toward predominantly elastic behavior with the absence of G’/G” crossover, indicating increased molecular connectivity and network formation. Compared with conventional melt-state peroxide modification, the solid-state approach promotes intermolecular connectivity while limiting degradation pathways, providing an energy-efficient and scalable strategy for tailoring polypropylene properties.

Original languageEnglish
Pages (from-to)7516-7524
Number of pages9
JournalMacromolecules
Volume59
Issue number13
DOIs
Publication statusPublished - 14 Jul 2026

Keywords

  • SELECTIVELY LABELED POLYPROPYLENE
  • CRYSTALLIZATION BEHAVIOR
  • CROSS-LINKING
  • POLYMERS
  • DEGRADATION
  • PRODUCTS
  • KINETICS

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