Suppr超能文献

对牛顿流体扩展动力学的实验贡献:体积、粘度和表面活性剂的影响。

Experimental contribution to the understanding of the dynamics of spreading of Newtonian fluids: effect of volume, viscosity and surfactant.

机构信息

Département de Chimie Physique des Réactions, UMR 7630 CNRS-INPL, Nancy-Université, 1, rue Grandville, BP 20451, 54001 Nancy Cedex, France.

出版信息

J Colloid Interface Sci. 2010 Apr 1;344(1):180-97. doi: 10.1016/j.jcis.2009.12.039. Epub 2009 Dec 28.

Abstract

The dynamics of drop spreading of glycerol-water mixtures with and without surfactant on hydrophilic glass surfaces has been investigated. The influence of different factors, such as viscosity, drop volume and non-ionic alkyl (8-16) glucoside (Plantacare) surfactant concentration on the number and the nature of the spreading regimes is systematically investigated. More than 25 spreading experiments have been performed in order to obtain clear trends. The results confirm the existence of several spreading regimes for the duration of an experiment (200 s). For each regime, the radius can be expressed by a power law of the form R=Kt(n). Both n and K are necessary to identify the regime. The experimental data are compared with the analytical predictions of the combined theory of spreading. One of the main results of this study is that the nature of the regimes is strongly affected by the drop volume, the viscosity and the surfactant concentration. This behavior is not predicted by the theory. For drop volume less than or equal to 15 microL, a succession of two different regimes which depend on the viscosity and surfactant concentration are observed in the following order: a molecular-kinetic regime followed by a hydrodynamic regime (for high viscosity in the presence of surfactant) or a hydrodynamic regime and lastly a final asymptotic regime corresponding to a long relaxation time to equilibrium (for high viscosity in absence of surfactant and for low viscosity regardless of the presence of surfactant). The spreading follows quantitatively the predictions of the theory. Our results demonstrate that the theory is still valid for low viscosity liquids and in the presence of surfactant. The contact angle for which the crossover between molecular-kinetic regime and hydrodynamic regime occurs is thoroughly estimated since the theories do not allow the exact calculation of this value. Here for the first time, an empirical power law exponent (n=0.08+/-0.05) is proposed for the last asymptotic regime since its quantitative estimation was not provided by the theory. For drop volume larger than 15 microL, the combined theory is still valid and the spreading process goes through a combination of two different regimes. In absence of surfactant, the succession of a molecular-kinetic regime and lastly a hydrodynamic regime, is demonstrated.

摘要

已经研究了甘油-水混合物在亲水玻璃表面上的液滴铺展的动力学,有无表面活性剂的情况。系统研究了不同因素(如粘度、液滴体积和非离子烷基(8-16)葡糖苷(Plantacare)表面活性剂浓度)对铺展区数量和性质的影响。为了获得清晰的趋势,进行了超过 25 次铺展实验。结果证实了在实验持续时间内存在几种铺展区(200 秒)。对于每个区域,半径可以表示为形式为 R=Kt(n)的幂律。n 和 K 都是识别区域所必需的。实验数据与铺展的综合理论的分析预测进行了比较。这项研究的主要结果之一是,区域的性质受到液滴体积、粘度和表面活性剂浓度的强烈影响。这种行为是理论无法预测的。对于体积小于或等于 15 微升的液滴,观察到两种不同区域的连续顺序,这取决于粘度和表面活性剂浓度:分子动力学区随后是流体动力区(在存在表面活性剂的情况下粘度较高)或流体动力区,最后是对应于长弛豫时间达到平衡的最终渐近区(在不存在表面活性剂的情况下粘度较高和在存在表面活性剂的情况下无论粘度如何)。铺展在定量上遵循理论的预测。我们的结果表明,该理论对于低粘度液体和存在表面活性剂的情况下仍然有效。由于理论不允许精确计算该值,因此彻底估计了发生分子动力学区和流体动力区之间交叉的接触角。这里首次提出了最后一个渐近区的经验幂律指数(n=0.08+/-0.05),因为该理论没有提供对其的定量估计。对于体积大于 15 微升的液滴,综合理论仍然有效,铺展过程经历两个不同区域的组合。在不存在表面活性剂的情况下,证明了分子动力学区和最后是流体动力区的连续顺序。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验