The mechanism leading to the extraordinary stability of bulk nanobubbles in aqueous solutions remains an outstanding problem in soft matter, modern surface science, and physical chemistry science. In this work, the stability of bulk nanobubbles in electrolyte solutions under different pH levels and ionic strengths is studied. Nanobubbles are generated via the technique of ultrasonic cavitation, and characterized for size, number concentration and zeta potential under ambient conditions. Experimental results show that nanobubbles can survive in both acidic and basic solutions with pH values far away from the isoelectric point. We attribute the enhanced stability with increasing acidity or alkalinity of the aqueous solutions to the effective accumulation of net charges, regardless of their sign. The kinetic stability of the nanobubbles in various aqueous solutions is evaluated within the classic DLVO framework. Further, by combining a modified Poisson-Boltzmann equation with a modified Langmuir adsorption model, we describe a simple model that captures the influence of ion species and bulk concentration and reproduce the dependence of the nanobubble's surface potential on pH. We also discuss the apparent contradiction between quantitative calculation by ion stabilization model and experimental results. This essentially requires insight into the structure and dynamics of interfacial water on the atomic-scale.
Keywords: Bulk nanobubble; Colloidal stability; Ion adsorption; Stability; Surface charge.
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