弹性体
材料科学
复合材料
纳米复合材料
聚合物
粒子(生态学)
体积分数
体积热力学
聚合物纳米复合材料
钢筋
填料(材料)
热塑性弹性体
天然橡胶
玻璃化转变
纳米颗粒
执行机构
纳米技术
高分子科学
拉伤
机制(生物学)
体积膨胀
变形(气象学)
分子动力学
作者
Pierre Kawak,Harshad Bhapkar,David Simmons
标识
DOI:10.1073/pnas.2528108123
摘要
For nearly a century, introduction of nanoparticles to elastomers has yielded extraordinarily tough nanocomposites that are critical to technologies from actuators to tires. The mechanisms by which this reinforcement occurs have nevertheless remained a central open question in material science. One widely debated hypothesis posits that strong interactions between polymer and particles induce "glassy bridges" that cement particles into a cohesive percolating network that resists elongation. Here, molecular dynamics simulations show that glassy particle shells do not primarily provide elongational cohesion. Instead, they amplify an underlying mechanism wherein competition between filler and elastomer networks causes the elastomer's volume to increase on deformation. This induces contributions from the elastomer's bulk modulus, which is of order 1,000 times larger than its Young's modulus. These findings establish a unified understanding of low-strain reinforcement in filled elastomers as emanating from volumetric competition between coexisting particulate and elastomeric networks. This reframes and unifies our understanding of low-strain reinforcement, provides a clear-cut diagnostic for the presence of glassy bridging, and offers a design principle for tough elastomeric nanocomposites.
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