粘弹性
共价键
统计物理学
口译(哲学)
聚合物
纳米技术
计算机科学
放松(心理学)
应力松弛
生化工程
高分子科学
化学物理
材料科学
化学
物理
热力学
心理学
工程类
有机化学
社会心理学
蠕动
程序设计语言
作者
Murillo L. Martins,Xiao Zhao,Zoriana Demchuk,Jiancheng Luo,Gregory Peyton Carden,Gaukhar Toleutay,Alexei P. Sokolov
出处
期刊:Macromolecules
[American Chemical Society]
日期:2023-11-03
卷期号:56 (21): 8688-8696
被引量:40
标识
DOI:10.1021/acs.macromol.3c01545
摘要
Polymers with dynamic covalent bonds are an exciting class of materials with properties and potential applications that rapidly gain significant attention from diverse scientific communities. While the number of publications on this emerging topic increases exponentially, navigating through this literature reveals a series of physical inconsistencies in previously established concepts and some misconceptions in data analysis and interpretation. The current paper presents an analysis of practices often applied to the characterization of systems with dynamic bonds and emphasizes particular misconceptions that may lead to critical divergences and misinterpretations of the results. We particularly focus on practices that should be avoided in the interpretation of stress–relaxation and viscoelastic data and in estimates of the bond dissociation energy. Instead, we suggest using traditional approaches that have been applied to the analysis of polymer viscoelastic properties for decades. Lastly, we emphasize the current challenges in a full understanding of the microscopic behavior of vitrimers.
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