战术性
粘弹性
流变学
材料科学
链条(单位)
平面的
应变硬化指数
电介质
分子动力学
聚合物
高分子化学
复合材料
刚度
硬化(计算)
化学物理
非线性系统
动力学(音乐)
结晶学
弹性(物理)
光谱学
量子纠缠
介电损耗
拉伤
化学
持续时间
魏森伯格数
结晶
作者
Shilong Wu,Xi Zeng,Qi-Lu Yuan,Huanhuan Yang,Wen-Sheng Xu,Quan Chen
出处
期刊:Macromolecules
[American Chemical Society]
日期:2026-01-23
卷期号:59 (3): 1371-1382
被引量:2
标识
DOI:10.1021/acs.macromol.5c02675
摘要
This study examines how the segmental and chain dynamics of poly(methyl methacrylate) (PMMA) depend on tacticity. Dielectric response spectroscopy reveals a much stronger β-relaxation peak, more clearly separated from the α-relaxation process at T < T g, for syndiotactic PMMA (sPMMA) than for isotactic PMMA (iPMMA). Linear viscoelastic measurements show similar rubbery plateaus for sPMMA and iPMMA, suggesting comparable entanglement molecular weights. In contrast, nonlinear extensional rheology exhibits substantially weaker strain hardening in sPMMA than in iPMMA. We propose that locally stiffer and more curved chain conformations in sPMMA reduce packing efficiency at T < T g, facilitating flippin g of planar ester groups that manifests as an enhanced β-relaxation in dielectric response spectroscopy. The same local stiffness probably leads to lower stretchability of the sPMMA chains, thereby leading to the weaker strain hardening at Weissenberg number much higher than one.
科研通智能强力驱动
Strongly Powered by AbleSci AI