Wu J, Bratko D, Prausnitz J M
Department of Chemical Engineering, University of California, and Chemical Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA.
Proc Natl Acad Sci U S A. 1998 Dec 22;95(26):15169-72. doi: 10.1073/pnas.95.26.15169.
How colloidal particles interact with each other is one of the key issues that determines our ability to interpret experimental results for phase transitions in colloidal dispersions and our ability to apply colloid science to various industrial processes. The long-accepted theories for answering this question have been challenged by results from recent experiments. Herein we show from Monte-Carlo simulations that there is a short-range attractive force between identical macroions in electrolyte solutions containing divalent counterions. Complementing some recent and related results by others, we present strong evidence of attraction between a pair of spherical macroions in the presence of added salt ions for the conditions where the interacting macroion pair is not affected by any other macroions that may be in the solution. This attractive force follows from the internal-energy contribution of counterion mediation. Contrary to conventional expectations, for charged macroions in an electrolyte solution, the entropic force is repulsive at most solution conditions because of localization of small ions in the vicinity of macroions. Both Derjaguin-Landau-Verwey-Overbeek theory and Sogami-Ise theory fail to describe the attractive interactions found in our simulations; the former predicts only repulsive interaction and the latter predicts a long-range attraction that is too weak and occurs at macroion separations that are too large. Our simulations provide fundamental "data" toward an improved theory for the potential of mean force as required for optimum design of new materials including those containing nanoparticles.
胶体粒子如何相互作用是决定我们解释胶体分散体系中相变实验结果的能力以及将胶体科学应用于各种工业过程的能力的关键问题之一。长期以来被接受的回答这个问题的理论受到了最近实验结果的挑战。在此我们通过蒙特卡罗模拟表明,在含有二价抗衡离子的电解质溶液中,相同的大离子之间存在短程吸引力。作为对其他人最近的一些相关结果的补充,我们提供了有力证据,证明在添加盐离子的情况下,对于相互作用的大离子对不受溶液中任何其他大离子影响的条件,一对球形大离子之间存在吸引力。这种吸引力源于抗衡离子介导的内能贡献。与传统预期相反,对于电解质溶液中的带电大离子,由于小离子在大离子附近的定位,熵力在大多数溶液条件下最多是排斥性的。德亚金 - 朗道 - 韦弗 - 奥弗贝克理论和相纸 - 伊势理论都无法描述我们模拟中发现的吸引相互作用;前者仅预测排斥相互作用,后者预测的长程吸引力太弱且发生在大离子间距太大的情况下。我们的模拟为改进平均力势理论提供了基础“数据”,这对于包括含纳米颗粒材料在内的新材料的优化设计是必需的。