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Elasticity, fracture and thermoreversible gelation of highly filled physical gels

机译:高填充物理凝胶的弹性,断裂和热可逆凝胶化

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We describe a physically associating triblock copolymer-based gel that exhibits a reversible transition between solid and liquid states at a temperature of approximately 55 degrees C. The thermal transition of the gel enables us to compare the properties of liquid suspensions and elastic composites with identical particle loadings, with particle volume fractions as large as 0.55. The suspension viscosity and the composite elasticity scale in a similar manner with the overall particle volume fraction, a result that is rationalized in terms of an effective strain amplification factor that depends only on the particle loading. Measured values of the strain amplification factor are in good agreement with the expected form for well-dispersed spheres. We also find that the elastic composites are exceptionally strong, with fracture strengths that exceed the modulus of the base gel by a factor of 100 or more. Deviations from purely elastic behavior became important for high particle volume fractions, and were probed by stress relaxation experiments.
机译:我们描述了一种基于物理缔合的三嵌段共聚物凝胶,该凝胶在大约55摄氏度的温度下在固态和液态之间呈现可逆转变。凝胶的热转变使我们能够比较具有相同颗粒的液体悬浮液和弹性复合材料的性能颗粒体积分数高达0.55。悬浮液粘度和复合弹性与总颗粒体积分数的比例相似,这是根据仅取决于颗粒载荷的有效应变放大因子来合理化的结果。应变放大因子的测量值与分散良好的球体的预期形式非常吻合。我们还发现,弹性复合材料异常坚固,其断裂强度比基础凝胶的模量高出100倍或更多。对于高颗粒体积分数,纯弹性行为的偏离变得很重要,并且通过应力松弛实验进行了探究。

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