On the phase-field modelling of a miscible liquid/liquid boundary

被引:7
|
作者
Xie, Ruilin [1 ]
Vorobev, Anatoliy [1 ]
机构
[1] Univ Southampton, Fac Engn & Environm, Energy Technol Res Grp, Southampton SO17 1BJ, Hants, England
关键词
Miscible liquids; Diffusive interface; Non-Fickian diffusion; Dynamic surface tension; Cahn-Hilliard approach; LASER LINE DEFLECTION; CAPILLARY TUBES; NUMERICAL SIMULATIONS; KORTEWEG STRESSES; NONUNIFORM SYSTEM; OIL-RECOVERY; FREE-ENERGY; DISPLACEMENTS; INTERFACES; TRANSITIONS;
D O I
10.1016/j.jcis.2015.11.026
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Mixing of miscible liquids is essential for numerous processes in industry and nature. Mixing, i.e. interpenetration of molecules through the liquid/liquid boundary, occurs via interfacial diffusion. Mixing can also involve externally or internally driven hydrodynamic flows, and can lead to deformation or disintegration of the liquid/liquid boundary. At the moment, the mixing dynamics remains poorly understood. The classical Fick's law, generally accepted for description of the diffusion process, does not explain the experimental observations, in particular, the recent experiments with dissolution of a liquid solute by a liquid solvent within a horizontal capillary (Stevar and Vorobev, 2012). We present the results of the numerical study aimed at development of an advanced model for the dissolution dynamics of liquid/liquid binary mixtures. The model is based on the phase-field (Cahn-Hilliard) approach that is used as a physics-based model for the thermo- and hydrodynamic evolution of binary mixtures. Within this approach, the diffusion flux is defined through the gradient of chemical potential, and, in particular, includes the effect of barodiffusion. The dynamic interfacial stresses at the miscible interface are also taken into account. The simulations showed that such an approach can accurately reproduce the shape of the solute/solvent boundary, and some aspects of the diffusion dynamics. Nevertheless, all experimentally-observed features of the diffusion motion of the solute/solvent boundary, were not reproduced. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:48 / 58
页数:11
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