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LONG-RANGE HYDRODYNAMIC INTERACTIONS ENHANCE COLLOIDAL GELATION

机译:长程水力相互作用增强胶体胶凝作用

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摘要

Colloidal gels are formed during arrested phase separation. Sub-micron, mutually attractive particles aggregate to form a system-spanning network with high interfacial area, far from equilibrium. Models for microstructural evolution during colloidal gelation have often struggled to match experimental results with long standing questions regarding the role of hydrodynamic interactions. In the present work, we demonstrate simulations of gelation with and without hydrodynamic interactions between the suspended particles. The disparities between these simulations are striking and mirror the experimental-theoretical mismatch in the literature. The hydrodynamic simulations agree with experimental observations, however. We explore a simple model of the competing transport processes in gelation that anticipates these disparities, and conclude that hydrodynamic forces are essential.
机译:在阻滞相分离过程中形成胶体凝胶。亚微米级,相互吸引的粒子聚集在一起,形成了一个具有高界面面积,远未达到平衡的跨越系统的网络。胶体凝胶化过程中的微结构演化模型通常难以与实验结果相匹配,长期以来一直存在关于流体动力相互作用作用的疑问。在目前的工作中,我们演示了在有和没有悬浮颗粒之间存在水动力相互作用的情况下的凝胶化模拟。这些模拟之间的差异令人震惊,并反映了文献中实验理论上的不匹配。然而,流体动力学模拟与实验观察结果一致。我们探索了胶凝中竞争性运输过程的简单模型,该模型可以预测这些差异,并得出结论,流体动力是必不可少的。

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