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If a number of literature studies point at the positive role of coupling materials with non-thermal plasma, particularly for Volatile Organic Compounds (VOC) removal, most of them focus on the direct plasma-material interaction to understand the coupling. However, a key contribution relies in the VOC–material interaction. Therefore, this study focuses on the adsorption step of targeted VOCs to provide a new insight on plasma–material coupling. The adsorption of acetone, used as probe VOC, is explored on two widespread coupling materials: TiO2 and CeO2. First, their behaviors are compared regarding acetone uptake. This process is reactive and creates other organic species than acetone on both surfaces. Second, the metal oxide behaviors are compared regarding ozone uptake. Interestingly, under typical VOC treatment configuration, i.e., with organics on their surfaces, ozone uptake is driven by the adsorbed organics, not directly by the metal oxides anymore. Finally, the ozonation of both materials, preliminary exposed to acetone, is explored through the evolution of the adsorbed organics and the corresponding mineralization, i.e., CO and CO2 formation. It evidences that the reactive adsorption of VOCs plays a key role in making the surface organics ready for an efficient oxidation and mineralization under post-plasma exposure.

In the context of coupling nonthermal plasmas with catalytic materials, CeO2 is used as adsorbent for toluene and combined with plasma for toluene oxidation. Two configurations are addressed for the regeneration of toluene saturated CeO2: (i) in plasma-catalysis (IPC); and (ii) post plasma-catalysis (PPC). As an advanced oxidation technique, the performances of toluene mineralization by the plasma-catalytic systems are evaluated and compared through the formation of CO2. First, the adsorption of 100 ppm of toluene onto CeO2 is characterized in detail. Total, reversible and irreversible adsorbed fractions are quantified. Specific attention is paid to the influence of relative humidity (RH): (i) on the adsorption of toluene on CeO2; and (ii) on the formation of ozone in IPC and PPC reactors. Then, the mineralization yield and the mineralization efficiency of adsorbed toluene are defined and investigated as a function of the specific input energy (SIE). Under these conditions, IPC and PPC reactors are compared. Interestingly, the highest mineralization yield and efficiency are achieved using the in-situ configuration operated with the lowest SIE, that is, lean conditions of ozone. Based on these results, the specific impact of RH on the IPC treatment of toluene adsorbed on CeO2 is addressed. Taking into account the impact of RH on toluene adsorption and ozone production, it is evidenced that the mineralization of toluene adsorbed on CeO2 is directly controlled by the amount of ozone produced by the discharge and decomposed on the surface of the coupling material. Results highlight the key role of ozone in the mineralization process and the possible detrimental effect of moisture.

Beyond tailored and synthetic catalysts sought out for ozone decomposition, mineral dusts provide naturally mixed metal oxide materials. The steady-state uptake of O3 evidenced across a wide concentration range signifies the catalytic decomposition of O3. The geocatalytic properties of such natural mineral dust open up new perspectives in atmospheric chemistry and catalytic processes.