Enhanced Piezocatalytic Performance of Li-doped BaTiO3 Through a Facile Sonication-Assisted Precipitation Approach.

Piezocatalysis-induced dye degradation has garnered significant attention as an effective method for addressing wastewater treatment challenges. In our study, we employed a room-temperature sonochemical method to synthesize piezoelectric barium titanate nanoparticles (BaTiO3: BTO) with varying levels of Li doping. This approach not only streamlined the sample preparation process but also significantly reduced the overall time required for synthesis, making it a highly efficient and practical method. One of the key findings was the exceptional performance of the Li-doped BTO nanoparticles. With 20 mg of Li additive, we achieved 90 % removal of Rhodamine B (RhB) dye within a relatively short timeframe of 150 minutes, all while subjecting the sample to ultrasonic vibration. This rapid and efficient dye degradation was further evidenced by the calculated kinetic rate constant, which indicated seven times faster degradation rate compared to pure BTO. The enhanced piezoelectric performance observed in the Li-doped BTO nanoparticles can be attributed to the strategic substitution of Li atoms, which facilitated a more efficient transfer of charge charges at the interface. Overall, our study underscores the potential of piezocatalysis coupled with advanced materials like Li-doped BTO nanoparticles as a viable and promising solution for wastewater treatment, offering both efficiency and environmental sustainability.

Insight into roles of carbon anodes for removal of refractory organic contaminants in electro-peroxone system: Mechanism, performance and stability.

Electro-peroxone (EP) is a novel technique for the removal of refractory organic contaminants (ROCs), while the role of anode in this system is neglected. In this work, the EP system with graphite felt anode (EP-GF) and activated carbon fiber anode (EP-ACF) was developed to enhance ibuprofen (IBP) removal. The results showed that 91.2% and 98.6% of IBP was removed within 20 min in EP-GF and EP-ACF, respectively. Hydroxy radical (O⋅H) was identified as the dominant reactive species, contributing 80.9% and 54.0% of IBP removal in EP-ACF and EP-GF systems, respectively. The roles of adsorption in EP-ACF and direct electron transfer in EP-GF cannot be ignored. Due to the differences in mechanism, EP-GF and EP-ACF systems were suitable for the removal of O⋅H-resistant ROCs (e.g., oxalic acid and pyruvic acid) and non-O⋅H-resistant ROCs (e.g., IBP and nitrobenzene), respectively. Both systems had excellent stability relying on the introduction of oxygen functional groups on the anode, and their electrolysis energy consumption was significantly lower than that of EP-Pt system. The three degradation pathways of IBP were proposed, and the toxicity of intermediates were evaluated. In general, carbon anodes have a good application prospect in the removal of ROCs in EP systems.

A highly accurate and semi-automated method for quantifying spherical microplastics based on digital slide scanners and image processing.

Microplastics (MPs), the emerging pollutants appeared in water environment, have grabbed significant attention from researchers. The quantitative method of spherical MPs is the premise and key for the study of MPs in laboratory researches. However, the manual counting is time-consuming, and the existing semi-automated analysis lacked of robustness. In this study, a highly accurate quantification method for spherical MPs, called VS120-MC was proposed. VS120-MC consisted of the digital slide scanner VS120 and the MPs image processing software, MPs-Counter. The full-area scanning photography was employed to fundamentally avoid the error caused by random or partition sampling modes. To accomplish high-performance batch recognition, the Weak-Circle Elimination Algorithm (WEA) and the Variable Coefficient Threshold (VCT) was developed. Finally, lower than 0.6% recognition error rate of simulated images with different aggregated indices was achieved by MPs-Counter with fast processing speed (about 2 s/image). The smallest size for VS120-MC to detect was 1 µm. And the applicability of VS120-MC in real water body was investigated. The measured value of 1 µm spherical MPs in ultra-pure water and two kinds of polluted water after digestion showed a good linear relationship with the Manual measurements (R2 = 0.982,0.987 and 0.978, respectively). For 10 µm spherical MPs, R2 reached 0.988 for ultra-pure water and 0.984 for both of the polluted water. MPs-Counter also showed robustness when using the same set of parameters processing the images with different conditions. Overall, VS120-MC eliminated the error caused by traditional photography and realized an accurate, efficient, stable image processing tool, providing a reliable alternative for the quantification of spherical MPs.

Electrochemically activated peroxymonosulfate with mixed metal oxide electrodes for sulfadiazine degradation: Mechanism, DFT study and toxicity evaluation.

Electrochemically activated peroxymonosulfate with mixed metal oxide electrodes (EA-PMS-MMO/MMO) is an emerging advanced oxidation process. It performed well on the degradation of sulfadiazine (SDZ), whose removal rate reached 81.13% within 30 min. Both the MMO anode and cathode played an irreplaceable role in PMS activation. HO•, SO4•-, O2•- and 1O2 were confirmed to be the major reactive species in the system, among which 1O2 was the most abundant. The generation mechanism of the reactive species and the overall mechanism of the system were proposed. Four degradation pathways of SDZ were speculated based on density functional theory. The acute and chronic toxicity of SDZ and its degradation intermediates was evaluated by the quantitative structure-activity relationship method, and the overall toxicity was significantly reduced after the degradation by EA-PMS-MMO/MMO. The results show that EA-PMS-MMO/MMO affords a reliable technology for the degradation of organic contaminants and has promising potential for application.

Enhancement of H2O2 yield and TOC removal in electro-peroxone process by electrochemically modified graphite felt: Performance, mechanism and stability.

Electro-peroxone (EP) is an emerging advanced oxidation process which combines electro-generation H2O2 and ozone for removing organic contaminants. In this paper, a platinum plate as anode, a method of electrochemical oxidation is adopted to modify graphite felt (GF) cathode to promote H2O2 yield and TOC removal from oxalic acid solution in EP process, its performance, mechanism and stability were discussed. Compared with original GF cathode, 2.6 times H2O2 yield can be achieved by the 5 min electrochemically modified GF (GF-5). The high electrochemical activity of the modified GF can be ascribed to introducing numerous surface oxygen-containing functional groups (OGs), which not only decreased the impedance, but also increased the amount of active site of O2 reduction. The production of H2O2 with GF-5 cathode improved with the increased initial pH, cathodic potential and O2 flow rate, while this promoting effect was not observed in GF cathode. Compared with GF cathode, TOC removal rate was improved by 21.5% with GF-5 cathode due to higher H2O2 yield in EP process. The primary pathway of TOC removal is electrochemically-driven peroxone process, and hydroxyl radical (·OH) is the dominant reactive species. Furthermore, GF-5 cathode had a good stability due to the protection of H2O2 and free electrons injected. The results indicate that the electrochemically modified GF severed as the cathode of EP processes has significant efficiency and stability in the removal of ozone-refractory organic contaminants.

Effect of ammonia stress on carbon metabolism in tolerant aquatic plant-Myriophyllum aquaticum.

In this study, the tips of Myriophyllum aquaticum (M. aquaticum) plants were planted in open-top plastic bins and treated by simulated wastewater with various ammonium-N concentrations for three weeks. The contents of related carbohydrates and key enzyme activities of carbon metabolism were measured, and the mechanisms of carbon metabolism regulation of the ammonia tolerant plant M. aquaticum under different ammonium-N levels were investigated. The decrease in total nonstructural carbohydrates, soluble sugars, sucrose, fructose, reducing sugar and starch content of M. aquaticum were induced after treatment with ammonium-N during the entire stress process. This finding showed that M. aquaticum consumed a lot of carbohydrates to provide energy during the detoxification process of ammonia nitrogen. Moreover, ammonia-N treatment led to the increase in the activitives of invertase (INV) and sucrose synthase (SS), which contributed to breaking down more sucrose to provide substance and energy for plant cells. Meanwhile, the sucrose phosphate synthase (SPS) activity was also enhanced under stress of high concentrations of ammonium-N, especially on day 21. The result indicated that under high-concentration ammonium-N stress, SPS activity can be significantly stimulated by regulating carbon metabolism of M. aquaticum, thereby accumulating sucrose in the plant body. Taken together, M. aquaticum can regulate the transformation of related carbohydrates in vivo by highly efficient expression of INV, SPS and SS, and effectively regulate the osmotic potential, thereby delaying the toxicity of ammonia nitrogen and improving the resistance to stress. It is very important to study carbon metabolism under ammonia stress to understand the ammonia nitrogen tolerance mechanism of M. aquaticum.