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Interphase Induced Dynamic Self-Stiffening in Graphene-Based Polydimethylsiloxane Nanocomposites

机译:石墨烯基聚二甲基硅氧烷纳米复合材料的相间诱导动态自增强

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The ability to rearrange microstructures and self-stiffen in response to dynamic external mechanical stimuli is critical for biological tissues to adapt to the environment. While for most synthetic materials, subjecting to repeated mechanical stress lower than their yield point would lead to structural failure. Here, it is reported that the graphene-based polydimethylsiloxane (PDMS) nanocomposite, a chemically and physically cross-linked system, exhibits an increase in the storage modulus under low-frequency, low-amplitude dynamic compressive loading. Cross-linking density statistics and molecular dynamics calculations show that the dynamic self-stiffening could be attributed to the increase in physical cross-linking density, resulted from the re-alignment and re-orientation of polymer chains along the surface of nanofillers that constitute an interphase. Consequently, the interfacial interaction between PDMS-nano-fillers and the mobility of polymer chain, which depend on the degree of chemical cross-linking and temperature, are important factors defining the observed performance of self-stiffening. The understanding of the dynamic self-stiffening mechanism lays the ground for the future development of adaptive structural materials and bio-compatible, load-bearing materials for tissue engineering applications.
机译:响应动态外部机械刺激而重新排列微观结构和自我增强的能力对于生物组织适应环境至关重要。对于大多数合成材料而言,反复承受低于其屈服点的机械应力会导致结构破坏。在这里,据报道,基于石墨烯的聚二甲基硅氧烷(PDMS)纳米复合材料是一种化学和物理交联的系统,在低频,低振幅动态压缩载荷下显示出储能模量的增加。交联密度统计数据和分子动力学计算表明,动态自刚度可归因于物理交联密度的增加,这是由于聚合物链沿着构成纳米管的纳米填料表面的重新排列和重新取向而导致的。相间。因此,PDMS-纳米填料之间的界面相互作用与聚合物链的迁移性(取决于化学交联程度和温度)是定义观察到的自增强性能的重要因素。对动态自加强机制的理解为将来用于组织工程应用的自适应结构材料和生物相容性承重材料奠定了基础。

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