Entanglement Network Suppresses Toughness Deterioration in Polycarbonate at Superhigh Strain Rates

IF 4.3 3区 化学 Q2 POLYMER SCIENCE
Macromolecular Rapid Communications Pub Date : 2026-03-06 Epub Date: 2025-12-22 DOI:10.1002/marc.202500940
Peng Dong, Jian-Bin Tang, Han Shang, Lei Li, Hao Lin, Gan-Ji Zhong, Zhong-Ming Li
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引用次数: 0

Abstract

The influence of molecular chain entanglement on the mechanical performance of polycarbonate (PC) at superhigh strain rates has been investigated, which is valuable for its safety applications like window glazing. The mechanical testing results across a wide strain rate range (0.01–100 s−1) show that toughness increases with strain rate, but significant deterioration of stiffness and toughness occurs at 100 s−1. This phenomenon is, for the first time, observed in real time using digital image correlation (DIC), revealing severe stress concentration and strain localization at 100 s−1. Nevertheless, we find this deterioration is significantly suppressed by the high entanglement density. It strengthens the strain hardening regime and dynamic mechanical analysis (DMA) is showing that both loss modulus and tan δ values increase with entanglement density in the β-relaxation region, indicating enhanced energy dissipation, which may be the underlying origin of the improved ability to resist deformation. This work is providing fundamental insights into tailoring entanglement networks to suppress energy absorption deterioration under extreme deformation conditions.

Abstract Image

缠结网络抑制超高应变速率下聚碳酸酯的韧性退化。
研究了超高应变速率下分子链缠结对聚碳酸酯(PC)力学性能的影响,为其在窗户玻璃等安全领域的应用提供了理论依据。在较宽应变速率范围内(0.01 ~ 100 s-1)的力学测试结果表明,随着应变速率的增加,韧性增加,但在100 s-1时刚度和韧性明显下降。这一现象首次通过数字图像相关(DIC)实时观察到,揭示了100 s-1下严重的应力集中和应变局部化。然而,我们发现高纠缠密度显著地抑制了这种劣化。动态力学分析(DMA)表明,在β-松弛区,损耗模量和tan δ值随着缠结密度的增加而增加,表明能量耗散增强,这可能是抗变形能力提高的根本原因。这项工作为在极端变形条件下裁剪纠缠网络以抑制能量吸收退化提供了基本见解。
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来源期刊
Macromolecular Rapid Communications
Macromolecular Rapid Communications 工程技术-高分子科学
CiteScore
7.70
自引率
6.50%
发文量
477
审稿时长
1.4 months
期刊介绍: Macromolecular Rapid Communications publishes original research in polymer science, ranging from chemistry and physics of polymers to polymers in materials science and life sciences.
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