Dixit N M, Zukoski C F
Department of Chemical Engineering, University of Illinois at Urbana-Champaign, 114 Roger Adams Laboratory, 600 South Mathews Avenue, Urbana, Illinois 61801, USA.
Phys Rev E Stat Nonlin Soft Matter Phys. 2001 Oct;64(4 Pt 1):041604. doi: 10.1103/PhysRevE.64.041604. Epub 2001 Sep 24.
We propose a kinetic model for describing crystal nucleation kinetics in hard-sphere colloidal suspensions. The model captures the interplay between the enhanced thermodynamic driving force and the reduced particle diffusivity in determining crystal nucleation rates as the particle density is increased in hard-sphere suspensions. Model calculations of nucleation rates and crystal growth velocities agree quantitatively with experimental observations. The dependence of the critical cluster size on volume fraction that emerges differs qualitatively from predictions of classical theories allowing for an experimental validation of the mechanism of crystal nucleation in colloidal suspensions.
我们提出了一个动力学模型,用于描述硬球胶体悬浮液中的晶体成核动力学。该模型捕捉了在硬球悬浮液中随着颗粒密度增加,增强的热力学驱动力和降低的颗粒扩散率在决定晶体成核速率方面的相互作用。成核速率和晶体生长速度的模型计算结果与实验观测在数量上相符。出现的临界团簇尺寸对体积分数的依赖性在性质上不同于经典理论的预测,这使得对胶体悬浮液中晶体成核机制进行实验验证成为可能。