Abstract

Hypothesis.The origin of the negative charge at water/air interface was proved to be not only specific adsorption of OH– ions but that of HCO3– and/or CO32– 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 NaHCO3 and Na2CO3.Experiments.Equilibrium thickness (equivalent thickness at equilibrium) of the foam films formed from aqueous solutions of NaHCO3 and Na2CO3 was measured as a function of electrolyte concentration at 298.15 K.Findings.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 NaHCO3 and Na2CO3 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 HCO3– 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 CO32–≫ HCO3–> OH–≫ Cl-.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call