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整个流体状态下带电二氧化硅球体悬浮液的结构与短时间动力学

Structure and short-time dynamics in suspensions of charged silica spheres in the entire fluid regime.

作者信息

Gapinski J, Patkowski A, Banchio A J, Buitenhuis J, Holmqvist P, Lettinga M P, Meier G, Nägele G

机构信息

Faculty of Physics, A. Mickiewicz University, 61-614 Poznan, Poland.

出版信息

J Chem Phys. 2009 Feb 28;130(8):084503. doi: 10.1063/1.3078408.

Abstract

We present an experimental study of short-time diffusion properties in fluidlike suspensions of monodisperse charge-stabilized silica spheres suspended in dimethylformamide. The static structure factor S(q), the short-time diffusion function D(q), and the hydrodynamic function H(q) have been probed by combining x-ray photon correlation spectroscopy experiments with static small-angle x-ray scattering. Our experiments cover the full liquid-state part of the phase diagram, including de-ionized systems right at the liquid-solid phase boundary. We show that the dynamic data can be consistently described by the renormalized density fluctuation expansion theory of Beenakker and Mazur over a wide range of concentrations and ionic strengths. In accordance with this theory and Stokesian dynamics computer simulations, the measured short-time properties cross over monotonically, with increasing salt content, from the bounding values of salt-free suspensions to those of neutral hard spheres. Moreover, we discuss an upper bound for the hydrodynamic function peak height of fluid systems based on the Hansen-Verlet freezing criterion.

摘要

我们展示了一项关于悬浮在二甲基甲酰胺中的单分散电荷稳定二氧化硅球体的类流体悬浮液中短时间扩散特性的实验研究。通过将X射线光子相关光谱实验与静态小角X射线散射相结合,对静态结构因子S(q)、短时间扩散函数D(q)和流体动力学函数H(q)进行了探测。我们的实验涵盖了相图的整个液态部分,包括液 - 固相边界处的去离子体系。我们表明,在广泛的浓度和离子强度范围内,动态数据可以由Beenakker和Mazur的重整化密度涨落展开理论一致地描述。根据该理论和斯托克斯动力学计算机模拟,随着盐含量的增加,测量到的短时间特性从无盐悬浮液的边界值单调过渡到中性硬球的边界值。此外,我们基于Hansen - Verlet冻结准则讨论了流体系统流体动力学函数峰值高度的上限。

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