4.7 Article

Insights into the mechanism of electrostatic field promoting ozone mass transfer in water: A molecular dynamics perspective

Journal

SCIENCE OF THE TOTAL ENVIRONMENT
Volume 848, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.scitotenv.2022.157710

Keywords

Ozone; Mass transfer; Gas-liquid interface; External electrostatic field; molecular dynamics

Funding

  1. National Natural Science Foundation of China [51408525]
  2. University Science and Technology Research Projects of Hebei Province [ZD2020324]
  3. Central Guidance on Local Science and Technology Development Fund of Hebei Province [216Z3601G]
  4. Natural Science Foundation of Hebei Province [E2022203061]

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This study investigates the effect of an external electrostatic field (EF) on the solubility and mass transfer characteristics of ozone in water. The results show that the presence of EF can increase the solubility of ozone, reduce the surface tension and viscosity at the gas-liquid interface, disrupt the hydrogen bond network in the liquid phase, and enhance the mobility of ozone.
Ozone is the main role of ozone-based advanced oxidation process for organic wastewater treatment, which is usually added in water by aeration. however, the low solubility of ozone in water seriously affects the degradation efficiency. In this article, the external electrostatic field (EF) was proposed to improve the ozone solubility in water. The mass transfer characteristics of ozone in a gas-liquid two-phase system under EF were studied by molecular dynamics (MD) simulation. The microscopic mechanism of ozone mass transfer in water promoted by external EF was revealed by analyzing Gibbs dividing surface (GDS) interface structure, interfacial water molecular orientation, surface tension, liquid phase viscosity, hydrogen bond network and ozone self-diffusion coefficient. Our findings reveal that Rican enhance the thickness of GDS region (from 0.4648 nm to 0.4996 nm when EF is 0.2 V/nm) as well as its ozone content. The dipole moment orientation of water molecules also tends to point in the EF direction due to the influence of EF, making the difference in dipole moment orientation of water molecules in the first and second layers of GDS region gradually disappear. In addition, compared with the absence of EF, the existence of external EF can decrease the surface tension (from 77.6162 mN/m to 73.3480 mN/m when EF is 0.2 V/nm) at the gas-liquid interface and the viscosity of liquid phase (from 0.293 mP(a).s to 0.162 mP(a).s when EF is 0.2 V/nm), break the network of hydrogen bond in liquid phase, and increase the mobility of ozone (self-diffusion coefficient of ozone changes from 1.3232 x 10(-6) cm(2).s(-1) to 1.8812 x 10(-6) cm(2).s(-1) when FF is 0.2 V/nm). All these properties changes indicate that the presence of external 1.1 enhances the ability of ozone to penetrate the interface of the two-phase system, and then improves the ozone mass transfer efficiency in water.

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