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Polyolefin blends with co-continuous architectures enabled by dynamic covalent crosslinking

  • Eliza K. Neidhart
  • , Stephanie M. Ribet
  • , Taehyun A. Lee
  • , Logan Kearney
  • , Karen C. Bustillo
  • , Eric A. Dailing
  • , Mutian Hua
  • , Colin Ophus
  • , Sophia N. Fricke
  • , Ah-Young Song
  • , Jeffrey A. Reimer
  • , Erik J. Alexanian
  • , Joanna M Atkin
  • , Brett A. Helms
  • , Frank A. Leibfarth
  • The University of North Carolina at Chapel Hill
  • Lawrence Berkeley National Laboratory
  • Oak Ridge National Laboratory
  • University of Washington
  • Civ. and Environ. Eng. Department
  • University of California, Berkeley
  • Berkeley College of Chemistry

Research output: Contribution to journalArticlepeer-review

Abstract

Blending polymers produces brittle materials due to macrophase separation and poor interfacial adhesion, which is exemplified by mixtures of polyolefins. This presents a formidable challenge for the mechanical recycling of mixed plastic waste. Here, we demonstrate that dynamic covalent crosslinking of immiscible polyolefin blends creates macrophase separated co-continuous architectures, yet they display excellent mechanical properties, which challenges the conventional wisdom regarding morphology-property relationships in polymer blend compatibilization. We find that the position and orientation of dynamic crosslinks and their influence on crystallinity are key to understanding the structure-morphology-property relationships. In particular, high-resolution microscopy imaging reveals alignment of crystallite planes with strong orientational preference, particularly at polymer-polymer interfaces, which contribute to material performance. We further demonstrate that changes in crosslinker density and valency allow the properties of binary and ternary polyolefin blends to be tuned in a modular fashion.
Original languageEnglish
Article numbereaee2328
Pages (from-to)1-11
Number of pages11
JournalScience Advances
Volume12
Issue number20
DOIs
StatePublished - Jan 1 2026

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