Meijia Gong, Luping Wang, Kaiyang Hou, Kaiqiang Zhang, Xu Wang
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引用次数: 0
Abstract
Optimizing supramolecular interactions is crucial for enhancing the damage resistance of elastomers under extreme mechanical stresses. However, the underlying mechanisms remain not fully understood, making targeted design challenging. This study thoroughly investigates a series of polyurethane elastomers and presents a strategy to enhance elastomer damage resistance by tuning the number and strength of hydrogen bonds at the hard–soft interface. Within these elastomers, we find that the hardness is positively correlated with the number and strength of hydrogen bonds, while toughness increases with the number of hydrogen bonds, reaching a maximum at moderate bond strength. Elastomers with both high hardness and toughness demonstrate superior impact resistance, while the best tear resistance is achieved with moderate hardness and high toughness. By balancing hydrogen bond acceptors in the soft segment with donors in the hard segment, an elastomer with an exceptional impact strength of 9.2 MJ m–2 is obtained, and tear resistance of 275.0 kJ m–2 is achieved by modulating the interaction strength. This research clarifies structural factors influencing damage resistance, including the number and strength of hydrogen bonds at the hard–soft interface, offering valuable insights for the design of highly impact- and tear-resistant elastomers.
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.