RESUMO
Although several non-thermal plasmas (NTPs) technologies have been widely investigated in air treatment, very few studies have focused on the inactivation mechanism of viruses by NTPs. Due to its efficiency and environmental compatibility, non-thermal plasma could be considered a promising virus-inactivation technology. Plasma is a partly or fully ionized gas including some species (i.e., electrons, free radicals, ions, and neutral molecules) to oxidize pollutants or inactivate harmful organisms. Non-thermal plasmas are made using less energy and have an active electron at a much higher temperature than bulk gas molecules. This review describes NTPs for virus inactivation in indoor air. The different application processes of plasma for microorganism inactivation at both laboratory and pilot-scale was also reviewed This paper reports on recent advances in this exciting area of viral inactivation identifying applications and mechanisms of inactivation, and summarizing the results of the latest experiments in the literature. Moreover, special attention was paid to the mechanism of virus inactivation. Finally, the paper suggests research directions in the field of airborne virus inactivation using non-thermal plasma.
Assuntos
Coronavirus , Gases em Plasma , Temperatura Alta , Tecnologia , Inativação de VírusRESUMO
In this study, we show that the combination of a photocatalytic process (as a pretreatment step) combined with the conventional biological treatment of wastewaters can improve the process and achieve satisfactory efficiency. In this context, Reactive Green 12 (RG-12) solutions were photocatalytically pretreated using TiO2-impregnated polyester as supported catalyst under UV light in batch reactor. Photocatalysis as pretreatment (during 4 and 8 h of irradiation) was combined with 7 days of aerobic biological treatment using activated sludge. As first assays, respiratory tests revealed that the removal of RG-12 was improved by 5.4% and 11.7% for the solutions that were irradiated for 4 and 8 h in the presence of TiO2, respectively. However, 34.5% and 19% of dye solution was discolored after 7 days of biological treatment for the pretreated solutions during 4 and 8 h of UV light exposure, respectively. The discoloration efficiency obtained by the combined processes achieved 59.6% and 74.9% for the samples under photocatalysis during 4 and 8 h, respectively. A significant decrease in chemical oxygen demand (COD) of about 74.9% was achieved after photocatalysis/biodegradation processes. In addition, a decrease in the phytotoxicity was obtained as followed by the germination index (GI) values of cress seeds that increased from 46.2 to 88.7% after 8 h of photocatalysis and then to 92.8% after further 7 days of biological treatment.
Assuntos
Germinação , Poluentes Químicos da Água , Catálise , Sementes , Esgotos , TitânioRESUMO
In the present study, we propose a new photocatalytic interface prepared by high-power impulse magnetron sputtering (HiPIMS), and investigated for the degradation of Reactive Green 12 (RG12) as target contaminant under visible light light-emitting diodes (LEDs) illumination. The CuxO/TiO2 nanoparticulate photocatalyst was sequentially sputtered on polyester (PES). The photocatalyst formulation was optimized by investigating the effect of different parameters such as the sputtering time of CuxO, the applied current, and the deposition mode (direct current magnetron sputtering, DCMS or HiPIMS). The results showed that the fastest RG12 degradation was obtained on CuxO/TiO2 sample prepared at 40 A in HiPIMS mode. The better discoloration efficiency of 53.4% within 360 min was found in 4 mg/L of RG12 initial concentration and 0.05% Cuwt/PESwt as determined by X-ray fluorescence. All the prepared samples contained a TiO2 under-layer with 0.02% Tiwt/PESwt. By transmission electron microscopy (TEM), both layers were seen uniformly distributed on the PES fibers. The effect of the surface area to volume (dye volume) ratio (SA/V) on the photocatalytic efficiency was also investigated for the discoloration of 4 mg/L RG12. The effect of the presence of different chemicals (scavengers, oxidant or mineral pollution or salts) in the photocatalytic medium was studied. The optimization of the amount of added hydrogen peroxide (H2O2) and potassium persulfate (K2S2O8) was also investigated in detail. Both, H2O2 and K2S2O8 drastically affected the discoloration efficiency up to 7 and 6 times in reaction rate constants, respectively. Nevertheless, the presence of Cu (metallic nanoparticles) and NaCl salt inhibited the reaction rate of RG12 discoloration by about 4 and 2 times, respectively. Moreover, the systematic study of reactive oxygen species' (ROS) contribution was also explored with the help of iso-propanol, methanol, and potassium dichromate as â¢OH radicals, holes (hâº), and superoxide ion-scavengers, respectively. Scavenging results showed that O2- played a primary role in RG12 removal; however, â¢OH radicals' and photo-generated holes' (hâº) contributions were minimal. The CuxO/TiO2 photocatalyst was found to have a good reusability and stability up to 21 cycles. Ions' release was quantified by means of inductively coupled plasma mass spectrometry (ICP-MS) showing low Cu-ions' release.