天然橡胶
复合材料
压缩永久变形
材料科学
弹性体
丁腈橡胶
腈
炭黑
极限抗拉强度
肿胀 的
断链
结构工程
化学
聚合物
工程类
有机化学
作者
Aaron M. Duncan,Keizo Akutagawa,Julien Ramier,James J. C. Busfield
出处
期刊:Macromolecules
[American Chemical Society]
日期:2023-08-22
卷期号:56 (17): 6704-6711
被引量:1
标识
DOI:10.1021/acs.macromol.3c01131
摘要
A new model is presented to predict rubber behavior during chemical aging at fixed strains. The model is validated using a carbon black-filled nitrile butadiene rubber aged in air at 125 °C. The model improves upon Tobolsky's dual network theory, designed for unfilled elastomers undergoing conventional aging but which has also often been used in rubber composites undergoing more complex aging scenarios. This work explores the shortcomings of the original model and demonstrates how the new model overcomes them. The model was validated using uniaxial tensile samples aged at 125 °C for 24-72 h at strains from 0-30%. The permanent set was measured, and the samples were tested on an Instron uniaxial test machine after aging. The cross-link density was estimated by equilibrium swelling. Results show that the new model more accurately models the stress-strain behavior to higher strains and provides more reliable estimates of chain scission and cross-linking after aging.
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