[Research Progress in Electrochemical Detection and Removal of Micro/Nano Plastics in Water].

Micro/nano plastics （M/NPs） are widely dispersed in the soil， atmosphere， and water environment due to their small particle size， easy adsorption， and strong migration， and have been detected in all major water bodies in recent years. As a type of emerging pollutant， the physiological toxicity of M/NPs has a great impact on human health. The current bottleneck in this research field lies in the precise detection and efficient removal of M/NPs. Electrochemical technology， owing to its advantages of simple portability， sensitivity， and low cost in the detection of M/NPs， has the advantages of environmental friendliness， controllable reaction， and high efficiency in the removal of M/NPs， demonstrating enormous application potential. Based on the pollution status of M/NPs， the application of electrochemical technology to the detection and removal of M/NPs in the water environment was elaborated and summarized. The electrochemical sensing methods of M/NPs and the principles and characteristics of sensor recognition of M/NPs were analyzed. The removal efficiency and influencing factors of M/NPs in water by electro-flocculation， electro-adsorption， electro-oxidation， and electro-reduction technologies were also discussed. The results indicated that the detection of M/NPs particles using electrochemical sensing methods exhibited good characterization performance， and M/NPs could be efficiently removed through electrochemical techniques such as electrocoagulation， electro-adsorption， electro-oxidation， and electro-reduction. The influencing factors of electrochemical technology on the detection and removal of M/NPs were mainly related to sensor devices， electrode materials， material interface regulation， parameter conditions， and reactor systems. In the future， researchers should focus on the design of sensors， the development of electrode materials， and the optimization of reaction processes， which are expected to realize the application of M/NPs from laboratory detection and removal to actual water bodies.

Effective degradation of polystyrene microplastics by Ti/La/Co-Sb-SnO2 anodes: Enhanced electrocatalytic stability and electrode lifespan.

Microplastics have been identified as an emerging pollutant that poses a risk to the aquatic environment, and it is a challenge to find a suitable removal process. Electrocatalytic oxidation (ECO) technology has shown promising performance in removing various persistent organic pollutants. In this study, we prepared a new anode for removing polystyrene microplastics (PS MPs) by ECO. Ti/La-Sb-SnO2 electrodes doped with the rare earth element La as the active layer were synthesized to enhance the electrocatalytic activity. The lifespan of the electrode was improved by doping Mn, Co, or Ru as an intermediate layer modification between the titanium (Ti) substrate and the La-Sb-SnO2 active layer, respectively. The experimental results indicated that the addition of three types of intermediate layers led to different degrees of decrease in the catalytic activity of the electrode and the degradation performance of PS MPs. The addition of the Co intermediate layer had a negligible effect on the catalytic activity and performance of the Ti/La-Sb-SnO2 anode for PS degradation. In addition, the electrode lifespan with Co intermediate layer was significantly prolonged, which was 4.54, 2.38, and 1.19 times higher than the electrode without intermediate layer and the electrode with Ru and Mn intermediate layer, respectively. Therefore, Co was determined to be the optimal choice as the intermediate layer, and the production technique for the Ti/La/Co-Sb-SnO2 anodes was carefully adjusted. The degradation efficiency of PS MPs was optimized at a heat treatment temperature of 400 °C and a Sn: Co material ratio of 5:1, with a removal rate of 28.0 %. The ECO treatment also resulted in more pronounced changes in the structure and functional groups of the MPs. Various alkyl cleavage and oxidation products were detected after the treatment, suggesting that the oxidant (hydroxyl radicals) strongly interacted with the MPs, leading to their degradation. Overall, this work provided a new insight into removing MPs in water through the use of modified electrodes.

Adsorption performance of nanoplastics in carbon filtration column.

Nanoplastics (NPs) are usually formed by the decomposition of large plastics, which will cause water pollution after entering the water body. Carbon filter column is used to adsorb and remove polystyrene nanoparticles (PSNPs). The influence of experimental conditions on adsorption was investigated and fitted by kinetic model. The results show that increasing the height of carbon filter column and decreasing the initial concentration of PSNPs and water flow rate can prolong the breakthrough time of carbon filter column. When the initial concentration of PSNPs is 0.8 mg L-1, the influent flow rate is 4 mL min-1 and the height of carbon filter bed is 8.5 cm, the removal effect is the best, and the depletion point of carbon filter column is extended to 48 h. Adams-Bohart model is suitable for describing the initial stage of adsorption. Thomas and Yoon-Nelson models can well describe the whole dynamic adsorption process of PSNPs, and Yoon-Nelson model can accurately predict the time required for 50% PSNPs to penetrate the carbon column. The adsorption mechanism of NPs by carbon filter column is mainly through the attachment sites and pore retention provided by particles on the surface of activated carbon. This study can provide new technical and theoretical support for the removal of NPs.

Preparation of Co/Cu-based bi-MOFs and the degradation of sulfamethoxazole by activated peracetic acid.

Compared with the common synthesis methods of metal-organic frameworks (MOFs), Co/Cu-based bi-MOFs composite catalyst CoXCu(10-X)-MOFs (X = 2, 4, 6, and 8) was prepared by a facile synthesis method at room temperature. The bi-MOFs composite catalyst was characterized by scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FTIR), and X-ray diffraction (XRD). The removal ability of sulfamethoxazole (SMX) by different Co:Cu rate bi-MOFs composite catalysts, single Co-based MOFs (zeolitic imidazolate framework-67, ZIF-67), and Cu-based MOFs (Hong Kong University of Science and Technology-1, HKUST-1) were investigated and the effects of peracetic acid (PAA) concentration, catalyst dosage, the common interfering substances (Cl-, HCO3-, SO42-, HA) in water, and SMX removal were investigated. Through the analysis of different free radical scavengers and the changes of surface elements before and after the reaction, the oxidation mechanism was further explored, and the stability of Co4Cu6-MOFs was explored through repeated recycling. The experimental results demonstrate that Co4Cu6-MOFs have a high catalytic activity for PAA. Co4Cu6-MOFs/PAA show the best removal effect of SMX under neutral conditions and the presence of Cl- and HCO3- can promote the removal of SMX.

Design, Synthesis and Structure-Activity Relationship of Novel Pinacolone Sulfonamide Derivatives against Botrytis cinerea as Potent Antifungal Agents.

To develop new fungicides with high efficiency, 46 novel sulfonamide derivatives were designed and synthesized by introducing pinacolone fragment into chesulfamide which was used as lead compound. All compounds were characterized by 1H NMR, 13C NMR, and MS spectra, and the structure of compound P-27 was also confirmed by X-ray single crystal diffraction. It was found that a variety of compounds present excellent inhibitory effect against Botrytis cinerea. The inhibition rates of P-29 on tomato and strawberry were 90.24% (200 mg/L) and 100% (400 mg/L) in vivo respectively, which were better than the lead compound chesulfamide (59.23% on tomato seedlings and 29.63% on strawberries).