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通过离子水合作用产生的特定离子效应:II. 双层相互作用。

Specific ion effects via ion hydration: II. Double layer interaction.

作者信息

Ruckenstein Eli, Manciu Marian

机构信息

Department of Chemical Engineering, State University of New York at Buffalo, Buffalo, NY 14260, USA.

出版信息

Adv Colloid Interface Sci. 2003 Sep 18;105:177-200. doi: 10.1016/s0001-8686(03)00068-x.

Abstract

A simple modified Poisson-Boltzmann formalism, which accounts also for those interactions between electrolyte ions and colloidal particles not included in the mean potential, is used to calculate the force between two parallel plates. It is shown that the short-range interactions between ions and plates, such as those due to the change in the hydration free energy of a structure-making/breaking ion that approaches the interface, affect the double layer interaction at large separations through the modification of the surface potential and surface charge density. While at short separations (below the range of the short-range ion-hydration forces) the interaction can be attractive, at larger separations the interaction is always repulsive, as in the traditional theory. When the long-range van der Waals interactions between the ions and the system (ion-dispersion interactions) are accounted for in the modified Poisson-Boltzmann approach, an attractive force between plates can be generated. At sufficiently large separations, this attraction can become even stronger than the traditional van der Waals attraction between plates of finite thickness, thus generating a dominant long-range 'double layer attraction'. At small plate separations, the attraction generated by the ion-dispersion forces combined with the electrostatic repulsion due to the double layers overlap can lead to a variety of interactions, from a weak attraction (which is typically by at least one order of magnitude smaller than the traditional van der Waals attraction between plates) to a strong double layer repulsion (for sufficiently large surface charges). Both types of ion interactions (long-range van der Waals or short-range ionic hydration) strongly affect the magnitude of the double layer interaction, and can account for the specific ion effects observed experimentally. However, they do not affect qualitatively the traditional theory of the colloid stability, which predicts that the colloid is stable when there is a sufficiently large charge on the surface, and coagulates when the van der Waals interactions between two colloidal particles dominate. The only qualitative difference found when the ion-dispersion interactions were incorporated into the traditional double layer theory was the emergence of a 'double layer attraction' at very large separations, which, however, does not affect much the stability of colloids.

摘要

一种简单的修正泊松 - 玻尔兹曼形式主义被用于计算两个平行板之间的力,该形式主义还考虑了电解质离子与胶体颗粒之间那些未包含在平均势中的相互作用。结果表明,离子与平板之间的短程相互作用,例如接近界面的结构形成/破坏离子的水化自由能变化所导致的相互作用,会通过改变表面电势和表面电荷密度来影响大间距时的双层相互作用。在短间距(低于短程离子水化力的范围)时,相互作用可能是吸引性的,而在较大间距时,如同传统理论一样,相互作用总是排斥性的。当在修正的泊松 - 玻尔兹曼方法中考虑离子与系统之间的长程范德华相互作用(离子 - 色散相互作用)时,平板之间会产生吸引力。在足够大的间距下,这种吸引力甚至可能比有限厚度平板之间的传统范德华吸引力更强,从而产生占主导地位的长程“双层吸引力”。在平板间距较小时,由离子 - 色散力产生的吸引力与双层重叠引起的静电排斥相结合,可能导致多种相互作用,从弱吸引力(通常比平板之间的传统范德华吸引力至少小一个数量级)到强双层排斥(对于足够大的表面电荷)。这两种离子相互作用(长程范德华或短程离子水化)都强烈影响双层相互作用的大小,并可以解释实验中观察到的特定离子效应。然而,它们在定性上并不影响胶体稳定性的传统理论,该理论预测当表面存在足够大的电荷时胶体是稳定的,而当两个胶体颗粒之间的范德华相互作用占主导时胶体就会凝聚。当将离子 - 色散相互作用纳入传统双层理论时,发现的唯一定性差异是在非常大的间距处出现了“双层吸引力”,然而,这对胶体的稳定性影响不大。

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