Department of Life and Environmental Science, Kagoshima Prefectural College, Kagoshima 890-0005, Japan.
J Colloid Interface Sci. 2022 Sep 15;622:652-661. doi: 10.1016/j.jcis.2022.04.116. Epub 2022 May 2.
The origin of the negative charge at water/air interface was proved to be not only specific adsorption of OH ions but that of HCO and/or CO ions in the previous study [1]. To determine which anionic species is primarily responsible for the surface charge, the surface density of ions in the Stern layer is numerically evaluated from foam-film thickness of aqueous solutions of NaHCO and NaCO.
Equilibrium thickness (equivalent thickness at equilibrium) of the foam films formed from aqueous solutions of NaHCO and NaCO was measured as a function of electrolyte concentration at 298.15 K.
Applying a modified Poisson-Boltzmann (PB) equation developed for various kinds of electrolytes to the equilibrium thickness gave the surface density of ions in the Stern layer for NaHCO and NaCO systems. From the concentration dependence of the surface density together with that for NaCl and NaOH in the previous study [1], the negative surface charges for water and very dilute solutions were found to be due to specific adsorption of HCO ions. The surface charge at high electrolyte concentration is determined by the specific adsorption of electrolyte anions. The specific-adsorption ability of anion increases in the order CO≫ HCO> OH≫ Cl.
在之前的研究中[1],已经证明水/气界面上的负电荷的起源不仅是 OH 离子的特殊吸附,还有 HCO 和/或 CO 离子的特殊吸附。为了确定哪种阴离子是表面电荷的主要责任,从 NaHCO 和 NaCO 水溶液的泡沫膜厚度数值评估了斯特恩层中离子的表面密度。
在 298.15 K 下,测量了由 NaHCO 和 NaCO 水溶液形成的泡沫膜的平衡厚度(平衡时的等效厚度)作为电解质浓度的函数。
将为各种电解质开发的改进的泊松-玻尔兹曼(PB)方程应用于平衡厚度,得到了 NaHCO 和 NaCO 体系中斯特恩层中离子的表面密度。从表面密度的浓度依赖性以及之前研究中 NaCl 和 NaOH 的表面密度[1],发现水和非常稀溶液的负表面电荷是由于 HCO 离子的特殊吸附。高电解质浓度下的表面电荷由电解质阴离子的特殊吸附决定。阴离子的特殊吸附能力按 CO>HCO>OH>Cl 的顺序增加。