Jiaoqin Liu

Organic pollutants like per- and polyfluoroalkyl substances (PFASs) exhibit persistence, bioaccumulation, resistance to degradation, and high toxicity, garnering significant attention from scholars worldwide. To better address and mitigate the environmental risks posed by PFASs, this paper employs bibliometric analysis to examine the literature on PFASs’ concentrations collected in the Web of Science (WoS) database between 2019 and 2024. The results show that the overall trend of PFASs’ pollution research is relatively stable and increasing. In addition, this study also summarizes the pollution status of traditional PFASs across different environmental media in typical freshwater basins. It analyzes PFASs’ concentrations in surface water, sediment, and aquatic organisms, elucidating their distribution characteristics and potential sources. While perfluorooctanoic acid (PFOA) and perfluorooctane sulfonic acid (PFOS) levels in water environments are declining annually, short-chain PFASs and their substitutes are emerging as primary pollutants. Short-chain PFASs are frequently detected in surface water, whereas long-chain PFASs tend to accumulate in sediments. In aquatic organisms, PFASs are more likely to concentrate in protein-rich organs and tissues. The environmental presence of PFASs is largely influenced by human activities, such as metal plating, fluoride industry development, and industrial wastewater discharge. Currently, the development of PFASs in China faces a complex dilemma, entangled by policy and legal constraints, industrial production demands, the production and use of new alternatives, and their regulation and restriction, creating a vicious cycle. Breaking this deadlock necessitates continuous and active scientific research on PFASs, particularly PFOS, with an emphasis on detailed investigations of environmental sources and sinks. Furthermore, ecological and health risk assessments were conducted using Risk Quotient (RQ) and Hazard Quotient (HQ) methods. Comprehensive comparison indicates that PFASs (such as PFOA) in the majority of freshwater basins are at a low-risk level (RQ < 0.1 or HQ < 0.2), PFOS in some freshwater basins is at a medium-risk level (0.1 < RQ < 1), and no freshwater basin is at a high-risk level. The adsorption and removal approaches of PFASs were also analyzed, revealing that the combination of multiple treatment technologies as a novel integrated treatment technology holds excellent prospects for the removal of PFASs.

2,2′,4,4′,6,6′-hexanitrostilbene (HNS) is a heat-resistant, low-sensitivity energetic material with widespread applications in pliable linear-shaped charges, high-temperature-resistant oil well perforating charges, and rocket propellants. However, the presence of highly toxic and mutagenic nitroaromatic compounds in HNS wastewater necessitates efficient and accurate detection methods. Unfortunately, the existing analytical methods for HNS detection are outdated and incompatible with modern equipment. This limits their application due to issues with detection range, accuracy, and cost. To address this gap, an improved method was developed using an Ultimate 3000 UHPLC system with methanol and water as the mobile phase and UV-Vis detection at 271 and 226 nm wavelengths. The results indicate that the optimal detection conditions are achieved with a methanol-to-water ratio of 70:30 and a flow rate of 0.5 mL/min, providing high accuracy and efficiency. Compared to traditional methods, this approach reduced the detection time by nearly 70%, with the shortest analysis time ranging from 6 to 6.5 min, significantly lowering the cost of HNS detection. The method demonstrated excellent linearity (R² > 0.9999) and high sensitivity within the concentration range of 0.50–150.00 mg/L, with precise and reliable results. This work provides both theoretical insights and experimental validation for the detection and analysis of HNS in wastewater.

With the development of the chemical industry, benzene, toluene, ethylbenzene, and xylene (BTEX) have gradually become the major indoor air pollutants. Various gas treatment techniques are widely used to prevent the physical and mental health hazards of BTEX in semi-enclosed spaces. Chlorine dioxide (ClO₂) is an alternative to chlorine as a secondary disinfectant with a strong oxidation ability, a wide range of action, and no carcinogenic effects. In addition, ClO₂ has a unique permeability which allows it to eliminate volatile contaminants from the source. However, little attention has been paid to the removal of BTEX by ClO₂, due to the difficulty of removing BTEX in semi-enclosed areas and the lack of testing methods for the reaction intermediates. Therefore, this study explored the performance of ClO₂ advanced oxidation technology on both liquid and gaseous benzene, toluene, o-xylene, and m-xylene. The results showed that ClO₂ was efficient in the removal of BTEX. The byproducts were detected by gas chromatography-mass spectrometry (GC-MS) and the reaction mechanism was speculated using the ab initio molecular orbital calculations method. The results demonstrated that ClO₂ could remove the BTEX from the water and the air without causing secondary pollution.

Background: As one of the modal antibiotics in life, the abuse of tetracycline (TC) caused great risks to the ecological environment and health. Cost‐effective removal method of TC in the medical wastewater was a developmental research direction with great potential.Results: In this work, a novel material, modified kaolin/β‐cyclodextrin (β‐CD) coated A (A is a special oxidant made from our laboratory, which is mainly composed of potassium ferrate) was synthesized and characterized. Meanwhile, the removal efficiencies and influencing factors of TC in novel material activation reaction systems were systematically studied. The specific surface area of modified kaolin (MMK) can reach up to 431.82 m²/g after acid and calcination modification. The results of SEM, TEM, XRD, and FT‐IR showed the significant increase in specific surface area of MMK was the complete destruction of kaolin structure and the leaching of aluminum. β‐CD was selected to coat A to attenuate the rapid release of A in water. The optimal coat molar ratio of β‐CD and A was 10: 1 (β‐CD:A). MMK/β‐CD‐A was used to treat the simulated TC wastewater, the removal efficiency was 95.6 % within 90 min when the concentration of TC was 0.22 mmol/L. The removal mechanism of TC with MMK/β‐CD‐A was the adsorption effect from MMK and the oxidation effect from β‐CD‐A.Conclusion: This work could provide useful information for developing a simple and effective technology to treat TC in medical wastewater. © 2023 Society of Chemical Industry (SCI).