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离子相关性对薄液膜表面力的影响:多价抗衡离子的影响及扩展理论

Effect of Ionic Correlations on the Surface Forces in Thin Liquid Films: Influence of Multivalent Coions and Extended Theory.

作者信息

Danov Krassimir D, Basheva Elka S, Kralchevsky Peter A

机构信息

Department of Chemical and Pharmaceutical Engineering, Faculty of Chemistry and Pharmacy, Sofia University, Sofia 1164, Bulgaria.

出版信息

Materials (Basel). 2016 Mar 1;9(3):145. doi: 10.3390/ma9030145.

Abstract

Experimental data for the disjoining pressure of foam films stabilized by anionic surfactant in the presence of 1:1, 1:2, 1:3, and 2:2 electrolytes: NaCl, Na₂SO₄, Na₃Citrate, and MgSO₄ are reported. The disjoining pressure predicted by the Derjaguin-Landau-Verwey-Overbeek (DLVO) theory coincides with the experimental data in the case of a 1:1 electrolyte, but it is considerably greater than the measured pressure in all other cases. The theory is extended to account for the effects of ionic correlations and finite ionic radii. Original analytical expressions are derived for the local activity coefficient, electrostatic disjoining pressure, and asymptotic screening parameter. With the same parameter of counterion binding as for a 1:1 electrolyte, the curves predicted by the extended theory are in perfect agreement with the experimental data for 1:2 and 1:3 electrolytes. In comparison with the DLVO theory, the effect of ionic correlations leads to more effective screening of electrostatic interactions, and lower electric potential and counterion concentrations in the film's midplane, resulting in lower disjoining pressure, as experimentally observed. The developed theory is applicable to both multivalent coions and multivalent counterions. Its application could remove some discrepancies between theory and experiment observed in studies with liquid films from electrolyte solutions.

摘要

报道了在1:1、1:2、1:3和2:2电解质(NaCl、Na₂SO₄、柠檬酸钠和MgSO₄)存在下,由阴离子表面活性剂稳定的泡沫膜的分离压力的实验数据。在1:1电解质的情况下,德亚金-朗道-韦弗-奥弗贝克(DLVO)理论预测的分离压力与实验数据相符,但在所有其他情况下,该理论预测的压力远大于实测压力。该理论得到扩展,以考虑离子相关性和有限离子半径的影响。推导了局部活度系数、静电分离压力和渐近屏蔽参数的原始解析表达式。在与1:1电解质相同的抗衡离子结合参数下,扩展理论预测的曲线与1:2和1:3电解质的实验数据完全吻合。与DLVO理论相比,离子相关性的影响导致静电相互作用的屏蔽更有效,膜中间平面的电势和抗衡离子浓度更低,从而导致分离压力更低,这与实验观察结果一致。所提出的理论适用于多价共离子和多价抗衡离子。其应用可以消除在电解质溶液液膜研究中观察到的理论与实验之间的一些差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bf5/5456698/a387d1e0215d/materials-09-00145-g009.jpg

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