Iyota Hidemi, Krastev Rumen
Department of Life and Environmental Science, Kagoshima Prefectural College, Kagoshima 890-0005, Japan.
Faculty of Applied Chemistry, Reutlingen University, Alteburgstraße 150, D-72762 Reutlingen, Germany.
J Colloid Interface Sci. 2020 Apr 1;565:405-415. doi: 10.1016/j.jcis.2019.12.042. Epub 2020 Jan 3.
The origin of negative surface charge at water/air interface is still not clear. The most probable origin is specific adsorption of OH ions. From diffuse layer potential, we can evaluate the surface density of ions in the Stern layer which can be a measure for the specific adsorption of ions and determines whether the surface charge is solely due to the specific adsorption of OH ions.
Equilibrium thickness of foam films of pure water and aqueous solutions of NaCl, HCl, and NaOH was measured as a function of disjoining pressure for water and as a function of concentration for the aqueous solutions at 298.15 K. Quartz-glass cells thoroughly cleaned and immersed in pure water before use were used for the measurement.
Application of a modified Poisson-Boltzmann equation to the equilibrium film thickness gave the diffuse layer potential and the surface density of ions in the Stern layer. From the concentration dependence of the surface density, it was concluded that not only OH ions but also Cl ions and HCO and/or CO ions adsorb specifically at the water/air interface.
水/空气界面处负表面电荷的起源仍不清楚。最可能的起源是OH离子的特异性吸附。根据扩散层电位,我们可以评估斯特恩层中离子的表面密度,这可以作为离子特异性吸附的一种度量,并确定表面电荷是否仅归因于OH离子的特异性吸附。
在298.15 K下,测量了纯水以及NaCl、HCl和NaOH水溶液的泡沫膜平衡厚度,作为水的分离压力的函数以及水溶液浓度的函数。测量使用的石英玻璃池在使用前经过彻底清洁并浸泡在纯水中。
将修正的泊松-玻尔兹曼方程应用于平衡膜厚度,得出了扩散层电位和斯特恩层中离子的表面密度。从表面密度对浓度的依赖性得出结论,不仅OH离子,而且Cl离子以及HCO和/或CO离子都会在水/空气界面处特异性吸附。