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Bibliographic Details
Main Authors: Wang, Shu, Hartquist, Chase M., Deng, Bolei, Zhao, Xuanhe
Format: Preprint
Published: 2024
Subjects:
Online Access:https://arxiv.org/abs/2401.16607
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author Wang, Shu
Hartquist, Chase M.
Deng, Bolei
Zhao, Xuanhe
author_facet Wang, Shu
Hartquist, Chase M.
Deng, Bolei
Zhao, Xuanhe
contents We present a loop-opening model that accounts for the molecular details of the intrinsic fracture energy for fracturing polymer networks. This model includes not only the energy released from the scission of bridging chains but also the subsequent energy released from the network continuum. Scission of a bridging chain releases the crosslinks and opens the corresponding topological loop. The released crosslinks will be caught by the opened loop to reach a new force-balanced state. The amount of energy released from the network continuum is limited by the stretchability of the opened loop. Based on this loop-opening process, we suggest that the intrinsics fracture energy per broken chain approximately scales with the product of the fracture force and the contour length of the opened loop. This model predicts an intrinsic fracture energy that aligns well with various experimental data on the fracture of polymer networks.
format Preprint
id arxiv_https___arxiv_org_abs_2401_16607
institution arXiv
publishDate 2024
record_format arxiv
spellingShingle A Loop-Opening Model for the Intrinsic Fracture Energy of Polymer Networks
Wang, Shu
Hartquist, Chase M.
Deng, Bolei
Zhao, Xuanhe
Materials Science
We present a loop-opening model that accounts for the molecular details of the intrinsic fracture energy for fracturing polymer networks. This model includes not only the energy released from the scission of bridging chains but also the subsequent energy released from the network continuum. Scission of a bridging chain releases the crosslinks and opens the corresponding topological loop. The released crosslinks will be caught by the opened loop to reach a new force-balanced state. The amount of energy released from the network continuum is limited by the stretchability of the opened loop. Based on this loop-opening process, we suggest that the intrinsics fracture energy per broken chain approximately scales with the product of the fracture force and the contour length of the opened loop. This model predicts an intrinsic fracture energy that aligns well with various experimental data on the fracture of polymer networks.
title A Loop-Opening Model for the Intrinsic Fracture Energy of Polymer Networks
topic Materials Science
url https://arxiv.org/abs/2401.16607