Stratification Dynamics in Drying Colloidal Mixtures

被引:80
|
作者
Howard, Michael P. [1 ]
Nikoubashman, Arash [2 ]
Panagiotopoulos, Athanassios Z. [1 ]
机构
[1] Princeton Univ, Dept Chem & Biol Engn, Princeton, NJ 08544 USA
[2] Johannes Gutenberg Univ Mainz, Inst Phys, Staudingerweg 7, D-55128 Mainz, Germany
基金
美国国家科学基金会;
关键词
DENSITY-FUNCTIONAL THEORY; HARD-SPHERE MIXTURES; MOLECULAR-DYNAMICS; SOLVENT EVAPORATION; FILM FORMATION; LIQUID-VAPOR; DISPERSIONS; FLUID; SIMULATIONS; EQUATION;
D O I
10.1021/acs.langmuir.7b00543
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Stratification in binary colloidal mixtures was investigated using implicit-solvent molecular dynamics simulations. For large particle size ratios and film Peclet numbers greater than unity, smaller colloids migrated to the top of the film, while big colloids were pushed to the bottom, creating an "inverted" stratification. This peculiar behavior was observed in recent simulations and experiments conducted by Forthii et al. [Phys. Rev. Lett. 2016, 116, 118301]. To rationalize this behavior, particle size ratios and drying rates spanning qualitatively different Pedet number regimes were systematically studied, and the dynamics of the inverted stratification were quantified in detail. The stratified layer of small colloids was found to grow faster and to larger thicknesses for larger size ratios. Interestingly,, inverted stratification was observed even at moderate drying rates where the film Pedet numbers were comparable to unity, but the thickness of the stratified layer decreased. A model based on dynamical density functional theory is proposed to explain the observed phenomena.
引用
收藏
页码:3685 / 3693
页数:9
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