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Contribution of the interphase interaction to the internal energy and thermodynamic properties of dispersed matrix composites

机译:相间相互作用对分散基复合材料内部能量和热力学性质的贡献

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This paper is devoted to the analysis of physical processes in composite matrix materials whose properties are greatly affected by the interphase interaction of the matrix and the modifier. Contribution of this interaction to thermodynamic and dielectric properties of such materials is investigated by the example of a model system which is a colloid solution of solid particles with charged surface in a polar liquid. Mechanisms underlying formation and stabilization of specific structures near the interphase boundaries of the examined system are discussed. Special attention is paid to the assessment of additional contribution to the internal energy and heat capacity related to the electric interaction of solid and liquid components. Results obtained within the proposed model show that for a certain concentration of liquid (about several percent) the interphase energy in a unit of volume magnificently increases to the values of about 10~7-10~8 J/m~3 and therefore exceeds heat motion energy of polar molecules. Moreover it was revealed that the electrical part of heat capacity is comparable to self-capacity of the liquid matrix provided that the surface charge density of solid particles is high enough.
机译:本文致力于分析复合基体材料的物理过程,这些材料的性能受基体与改性剂之间的相互作用影响很大。通过模型系统的实例研究了这种相互作用对此类材料的热力学和介电性能的贡献,该模型系统是具有带电表面的固体颗粒的胶体溶液在极性液体中的胶体溶液。讨论了被检查系统相间边界附近特定结构的形成和稳定机制。特别注意评估与固体和液体组分的电相互作用有关的内部能量和热容量的其他贡献。在所提出的模型中获得的结果表明,对于一定浓度的液体(大约百分之几),以体积为单位的相间能量急剧增加到大约10〜7-10〜8 J / m〜3的值,因此超过了热量极性分子的运动能。此外,揭示出,只要固体颗粒的表面电荷密度足够高,则热容量的电部分与液体基质的自容量相当。

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