# Propylene–Ethylene Copolymer Covalent Adaptable Networks Synthesized by Resonance‐Stabilized, Radical‐Based Reactive Processing with Excellent Elevated‐Temperature Creep Resistance

**Authors:** Yen‐Wen Huang, Mathew J. Suazo, Stephanie M. Barbon, Hayley A. Brown, Evelyn Auyeung, Colin Li Pi Shan, John M. Torkelson

PMC · DOI: 10.1002/cssc.202501137 · Chemsuschem · 2025-08-30

## TL;DR

Scientists created a new type of polymer network that resists deformation at high temperatures and can be reprocessed, solving a key issue with traditional polyolefins.

## Contribution

A one-step radical-based method to synthesize covalent adaptable networks with excellent creep resistance and reprocessability.

## Key findings

- The best-performing PEC CAN suppressed >99% of viscous creep at 160 °C over 600 s.
- The PEC CAN retained >98% creep resistance at 100 °C over 10,000 s.
- The PEC CAN is reprocessable via compression molding and twin-screw extrusion with full property recovery.

## Abstract

Low‐crystallinity propylene–ethylene copolymer (PEC) thermoplastics exhibit creep in the melt and semicrystalline states. To enhance creep resistance while maintaining reprocessability, dynamic covalent cross‐links are introduced through one‐step, radical‐based reactive processing to create covalent adaptable networks (CANs). During reactive processing, it is essential to suppress β‐scission of propylene repeat units. To promote the formation of resonance‐stabilized macroradical intermediates, a methacrylate‐based cross‐linker bis(4‐methacryloyloxyphenyl) disulfide (BPMA) is replaced with a phenylacrylate‐based cross‐linker bis(4‐phenacryloyloxyphenyl) disulfide (BPST) and styrene and divinylbenzene, vinyl aromatic additives, are incorporated. The use of BPST but not BPMA leads to percolated PEC CAN formation. Adding vinyl aromatic additives reduces the disparity in cross‐linking capability between BPMA and BPST. The resulting PEC CANs show markedly improved elevated‐temperature creep resistance compared to neat PEC. Relative to thermoplastic PEC, the best‐performing PEC CAN suppresses >99% of viscous creep at 160 °C (melt state) over 600 s and >98% at 100 °C (semicrystalline state) over 10,000 s. This top‐performing PEC CAN is reprocessable through compression molding and twin‐screw extrusion, achieving full recovery of cross‐link density and tensile properties. These results showcase a promising one‐step strategy for producing recyclable PEC CANs with enhanced creep resistance in melt and semicrystalline states, addressing critical limitations of low‐crystallinity polyolefins.

Propylene‐ethylene copolymer covalent adaptable networks (PEC CANs) are synthesized via one‐step, radical‐based reactive processing with the use of initiator, dynamic cross‐linkers, and vinyl aromatic additives. The best CAN suppresses over 98% of creep at 100 °C (semicrystalline state) for 10,000 s compared to neat PEC. The same CAN is reprocessable either through compression molding or twin‐screw extrusion.© 2025 WILEY‐VCH GmbH

## Linked entities

- **Chemicals:** propylene (PubChem CID 8252), ethylene (PubChem CID 6325), styrene (PubChem CID 7501), divinylbenzene (PubChem CID 66666)

## Full-text entities

- **Chemicals:** CAN (-), styrene (MESH:D020058), polyolefins (MESH:C035051), methacrylate (MESH:D008689), divinylbenzene (MESH:C004985)

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12548940/full.md

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12548940/full.md

## References

119 references — full list in the complete paper: https://tomesphere.com/paper/PMC12548940/full.md

---
Source: https://tomesphere.com/paper/PMC12548940