Oxidative degradation of rosslinked EPDM elastomers: Impact on the entanglement network

ABSTRACT The mechanical behavior of elastomers is mainly governed by the architecture of their macromolecular network. The increase in modulus observed during the oxidation of elastomers that predominantly undergo cross‐linking rather than chain scission can be described using the classical rubber elasticity theory. However, when chain scission becomes the main degradation process, the applicability of this theory may be questioned. This study investigates the relationship between the macromolecular network and the mechanical behavior of unfilled amorphous peroxide‐cured EPDMs by considering both the chemical cross‐link network and the physical entanglement network. The elastomers were characterized by equilibrium swelling and uniaxial tensile tests performed on unaged samples with different cross‐linker contents, as well as on oxidized samples exposed at 75°C, 90°C, and 100°C. Results clearly show that varying the cross‐linker content affects only the chemical cross‐link network without altering the entanglement density, whereas oxidation modifies both the chemical and entanglement networks. These findings provide new insights into the interplay between chemical cross‐links and physical entanglements during oxidation and highlight the limitation in using rubber elasticity theory when chain scission dominates the degradation process. They also emphasize the critical role of entanglements in the tensile behavior of unfilled elastomers.

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Publication Details

Journal
Journal of Polymer Science
Published
2026-05-01
DOI
https://doi.org/10.1002/pola.70144
Primary Topic
Polymer Nanocomposites and Properties
Type
article
Field-Weighted Citation Impact
0.00

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article

Oxidative degradation of rosslinked EPDM elastomers: Impact on the entanglement network

Paul Sotta, Bruno Fayolle, Maelenn Le Gall, Pierre‐Yves Le Gac et al.
Journal of Polymer Science
Polymer Nanocomposites and Properties
article

Oxidative degradation of rosslinked EPDM elastomers: Impact on the entanglement network

Paul Sotta, Bruno Fayolle, Maelenn Le Gall, Pierre‐Yves Le Gac, Maria Luísa Garbelini, Servane Haller, Guillaume Le Dain
article en

Abstract

ABSTRACT The mechanical behavior of elastomers is mainly governed by the architecture of their macromolecular network. The increase in modulus observed during the oxidation of elastomers that predominantly undergo cross‐linking rather than chain scission can be described using the classical rubber elasticity theory. However, when chain scission becomes the main degradation process, the applicability of this theory may be questioned. This study investigates the relationship between the macromolecular network and the mechanical behavior of unfilled amorphous peroxide‐cured EPDMs by considering both the chemical cross‐link network and the physical entanglement network. The elastomers were characterized by equilibrium swelling and uniaxial tensile tests performed on unaged samples with different cross‐linker contents, as well as on oxidized samples exposed at 75°C, 90°C, and 100°C. Results clearly show that varying the cross‐linker content affects only the chemical cross‐link network without altering the entanglement density, whereas oxidation modifies both the chemical and entanglement networks. These findings provide new insights into the interplay between chemical cross‐links and physical entanglements during oxidation and highlight the limitation in using rubber elasticity theory when chain scission dominates the degradation process. They also emphasize the critical role of entanglements in the tensile behavior of unfilled elastomers.

Journal of Polymer Science
Conservatoire National des Arts et Métiers (FR), Centre National de la Recherche Scientifique (FR), Ifremer (FR), Nexans (France) (FR), Ingenierie des Materiaux polymeres (FR), HESAM Université (FR), Institut National des Sciences Appliquées de Lyon (FR)
Agence Nationale de la Recherche
Openalex Percentile: Top 15%
Polymer Nanocomposites and Properties
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