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Segmented elastomers, such as polyurea, dissipate energy through various mechanisms. Although dynamic stiffening of soft domains is often cited, growing evidence highlights the dominant role of hydrogen-bond breaking and reformation. To clarify the specific role of hard domains, we synthesized polyurea, polyurethane, and polyurethane-urea with systematically varied hard-domain order, while maintaining comparable soft-domain dynamics at a target strain rate. Microballistic impact experiments revealed two distinct dissipation regimes, with ordered polyurea performing best. FTIR spectroscopy and strain-rate-dependent cyclic tension experiments confirmed an order–disorder transition coinciding with maximum energy dissipation. These findings emphasize the role of ordered hard domains in elastomer design.
Tan et al. (Mon,) studied this question.
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