Production and dispersion of free radicals from transient cavitation Bubbles: An integrated numerical scheme and applications

• Published in: Ultrasonics sonochemistry Vol. 88; p. 106067
• Main Authors: Peng, Kewen, Qin, Frank G.F., Jiang, Runhua, Qu, Wanjun, Wang, Qianxi
• Format: Journal Article
• Language: English
• Published: Elsevier B.V 01.08.2022; Elsevier
• Subjects: Dispersion; Free radicals; Production; Short Communication; Simulation; Sonochemistry; Free radicals; Sonochemistry; Simulation; Dispersion; Production
• ISSN: 1350-4177; 1873-2828
• DOI: 10.1016/j.ultsonch.2022.106067

•An integrated numerical scheme for simulating the complete radical production-dispersion.•The temporal-spatial distribution of the radicals in the liquid phase is presented.•The initiation reaction determines the overall intensity of radical productions.•The dispersion is constrained by the strong recombination reactions. As an advanced oxidation process with a wide range of applications, sonochemistry relies on acoustic cavitation to induce free radicals for degrading chemical contaminants. The complete process includes two critical steps: the radical production inside the cavitation bubble, and the ensuing dispersion of these radicals into the bulk solution. To grasp the physicochemical details in this process, we developed an integrated numerical scheme with the ability to quantitatively describe the radical production-dispersion behavior. It employs coupled simulations of bubble dynamics, intracavity chemical reactions, and diffusion–reaction-dominated mass transport in aqueous solutions. Applying this method to the typical case of argon and oxygen bubbles, the production mechanism for the main radicals is revealed. Moreover, the temporal-spatial distribution of the radicals in the liquid phase is presented. The results demonstrate that the enhanced radical production observed in oxygen bubbles can be traced to the initiation reaction O2 + H2O → OH+HO2, which requires relatively low activation energy. In the outside liquid region, the dispersion of radicals is limited by robust recombination reactions. The simulated penetration depth of OH is around 0.2 μm and agrees with reported experimental measurements. The proposed numerical approach can be employed to better capture the radical activity and is instrumental in optimizing the engineering application of sonochemistry.