Tensile Strain Softening of Associative Polymer Networks: Understanding Nonlinear Mechanics

IF 5.2 1区 化学 Q1 POLYMER SCIENCE
Cameron K. Locke,  and , Ying Yang*, 
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引用次数: 0

Abstract

Biological systems often exhibit strain stiffening to prevent deformation and softening to avoid catastrophic failure. Associative polymer networks are inspired by the dynamic nature of biomaterials and have broad applications as stimuli-responsive materials. Herein, we investigated the nonlinear extensional response of associative polymer networks with a focus on tensile strain softening. Metallo-supramolecular networks formed by pendant group cross-linking with different metal ions and a low degree of entanglements were used to access different network temporal parameters. While all networks exhibited shear-thinning, the ones with fast metal–ligand cross-links showed tensile strain softening with a yield point, while networks with slow cross-links did not. This indicates a fundamental difference in how associative networks respond to force under shear versus tensile deformations. The mechanism of yielding was explained by comparing the changing instantaneous extension rate at different stages of the tensile test with the network relaxation times probed by the sticky Rouse model and KWW fitting.

Abstract Image

Abstract Image

结合聚合物网络的拉伸应变软化:理解非线性力学
生物系统经常表现出应变硬化,以防止变形和软化,以避免灾难性的破坏。结合聚合物网络受到生物材料动态特性的启发,作为刺激响应材料具有广泛的应用。在此,我们研究了结合聚合物网络的非线性拉伸响应,重点是拉伸应变软化。利用悬垂基团与不同金属离子交联形成的金属超分子网络和低纠缠度的金属超分子网络来获取不同的网络时间参数。虽然所有网络都表现出剪切变薄,但具有快速金属配体交联的网络表现出具有屈服点的拉伸应变软化,而具有缓慢交联的网络则没有。这表明在剪切变形和拉伸变形下,联想网络对力的反应有根本区别。通过对比拉伸试验不同阶段瞬时延伸率的变化与粘性劳斯模型和KWW拟合探测的网络松弛时间,解释了屈服机理。
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来源期刊
Macromolecules
Macromolecules 工程技术-高分子科学
CiteScore
9.30
自引率
16.40%
发文量
942
审稿时长
2 months
期刊介绍: Macromolecules publishes original, fundamental, and impactful research on all aspects of polymer science. Topics of interest include synthesis (e.g., controlled polymerizations, polymerization catalysis, post polymerization modification, new monomer structures and polymer architectures, and polymerization mechanisms/kinetics analysis); phase behavior, thermodynamics, dynamic, and ordering/disordering phenomena (e.g., self-assembly, gelation, crystallization, solution/melt/solid-state characteristics); structure and properties (e.g., mechanical and rheological properties, surface/interfacial characteristics, electronic and transport properties); new state of the art characterization (e.g., spectroscopy, scattering, microscopy, rheology), simulation (e.g., Monte Carlo, molecular dynamics, multi-scale/coarse-grained modeling), and theoretical methods. Renewable/sustainable polymers, polymer networks, responsive polymers, electro-, magneto- and opto-active macromolecules, inorganic polymers, charge-transporting polymers (ion-containing, semiconducting, and conducting), nanostructured polymers, and polymer composites are also of interest. Typical papers published in Macromolecules showcase important and innovative concepts, experimental methods/observations, and theoretical/computational approaches that demonstrate a fundamental advance in the understanding of polymers.
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