Gas-phase oxidation of volatile organic compounds (VOCs) with the aid of ozone can be an attractive, energy-efficient way of treating exhaust gas streams in a low-temperature process, enabling the sustainable operation of industrial installations in a natural environment. This work is focused on the efficiency and kinetics of toluene oxidation with ozone towards CO2 and H2O in the presence of a SiO2-supported cobalt catalyst. A kinetic model is proposed based on a simplified reaction mechanism, with the parameters determined from measurements carried out in a fixed-bed reactor at 40–65 °C under conditions ensuring negligible mass transfer resistance. The proposed model provided satisfactory agreement between the predicted and measured toluene and ozone conversion rates and the formation rate of CO2, as well as in conditions when mass transfer resistance due to internal diffusion in the catalyst pellet was necessary to consider. The discussed results provide an assessment of the space velocity and ozone usage necessary to achieve a given degree of toluene conversion and mineralization to CO2. The proposed model can be used for the design of a sustainable, low-temperature ozone-assisted catalytic process of VOC abatement.
Machniewski et al. (Wed,) studied this question.