Mechanics of Physically Cross-Linked Hydrogels: Experiments and Theoretical Modeling

IF 5.2 1区 化学 Q1 POLYMER SCIENCE
Mohit Goswami, Agniva Dutta, Rishi Kulshreshtha, Gleb Vasilyev, Eyal Zussman, Konstantin Volokh
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引用次数: 0

Abstract

The remarkable ductility and enhanced toughness of metal–ligand-based hydrogels caused by physical cross-links that improve their mechanical properties have proven the efficacy of hydrogels in various engineering applications. Here, we bring the first comprehensive investigation of hydrogels under bulge testing. The multiaxial response of these materials is crucial for enhanced durability and load-bearing capability. In this study, we derive a hyperelastic constitutive model with a description of failure and validate it experimentally. The latter model is further used to analyze cavitation in these materials. This study demonstrates that incorporating imidazole–Ni2+ metal–ligand cross-links can significantly enhance several mechanical properties. For instance, increasing the imidazole content from 40 to 70 mol % improves the elastic modulus by 400% and the ultimate equibiaxial stress by 80%. The detailed experimental investigation reveals that the inflation of these hydrogels strongly depends on structural evolution. The current study paves the way for the development of novel experimental techniques and constitutive models to fine-tune the mechanical properties of hydrogels as per user requirements.

Abstract Image

物理交联水凝胶的力学:实验和理论建模
金属配体基水凝胶由于物理交联而具有显著的延展性和增强的韧性,从而改善了其力学性能,证明了水凝胶在各种工程应用中的有效性。在这里,我们首次对水凝胶在膨胀试验下进行了全面的研究。这些材料的多轴响应对增强耐久性和承载能力至关重要。在本研究中,我们推导了一个带有失效描述的超弹性本构模型,并进行了实验验证。后一种模型进一步用于分析这些材料中的空化现象。本研究表明,加入咪唑- ni2 +金属配体交联可以显著提高几种力学性能。例如,将咪唑含量从40 mol %增加到70 mol %,弹性模量提高400%,最终等双轴应力提高80%。详细的实验研究表明,这些水凝胶的膨胀强烈依赖于结构演化。目前的研究为开发新的实验技术和本构模型铺平了道路,可以根据用户的要求微调水凝胶的力学性能。
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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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