The main purpose of this paper was to reveal the effect of aluminum (Al)-based coagulants on enhanced coagulation for the removal of algae and the synergistic optimization mechanism among different Al species. The formation, breakage, and regrowth processes of algal coagulation flocs formed by a series of monomeric Al-based coagulants (Al₂(SO₄)₃, Al₁₃, and Al₃₀), Al₁₃/Al₃₀ composite coagulant and poly(diallyldimethylammonium chloride)/Al₁₃ (PDADMAC/Al₁₃) composite coagulant were studied. Results indicated that Al₁₃ mainly employed a charge neutralization mechanism, which was conducive to the destabilization of algae and the regeneration of flocs, while Al₃₀ mainly employed a sweep flocculation mechanism, which was conducive to the formation of algae and the strength of flocs. Meanwhile, the charge neutralization was the main mechanism during the algae coagulation process because it could effectively remove the soluble microbial products (SMP) component in the extracellular organic matter (EOM). Therefore, Al₁₃ could achieve a higher coagulation performance than other monomeric Al-based coagulants. The Al₁₃/Al₃₀ composite coagulant could make up for the deficiency of the sweep flocculation mechanism in Al₁₃ and charge neutralization mechanism in Al₃₀, and achieve the best synergistic optimization performance at Al₁₃:Al₃₀-7:3. Additionally, PDADMAC, as a polymer, could further enhance the charge neutralization ability of Al₁₃ at low dosages and the sweep flocculation ability of Al₁₃ at high dosages, respectively. However, an excessive dosage would lead to charge reversal and thus reduce the coagulation effect. Therefore, controlling the dosage was key when using Al-composite coagulants. The findings of our research could offer a certain theoretical foundation for the development of inorganic polymer flocculants.

Due to widespread industrial applications and increased discharges, concentrations of polyfluoroalkyl substances (PFAS) in potential drinking water sources have risen significantly, putting more people at risk of PFAS exposure. This study aimed to systematically clarify the occurrence characteristics (concentrations, detection frequencies, and temporal trends) of PFAS in global potential drinking water sources over the past decade, assess their oral exposure risks, and identify key PFAS species with high detection frequencies, high contamination levels, or high toxicity risks, thereby providing scientific support for the development of targeted control technologies and management strategies. This study systematically searched and reviewed the relevant literature published between 2014 and 2024 on PFAS levels in global potential drinking water sources, extracting data on PFAS concentrations, detection information, and sampling characteristics. Using the U.S. Environmental Protection Agency (EPA) Reference Dose (RfD) for oral exposure as the Acceptable Daily Intake (ADI), we evaluated the exposure risks of eight specific PFAS via the Risk Quotient for Specific Contaminants (RQ_RSC) model and analyzed the annual detection trends of the top thirty PFAS with the highest detection frequencies. Regarding total PFAS contamination, China, Brazil, Germany, South Africa, and the Danube River Basin exhibited particularly high levels, with China being the most severely contaminated. Risk assessment indicated that 45.6% of global potential drinking water sources were at high risk (RQ_RSC > 1), while 48.4% were at low risk (RQ_RSC < 0.2). Among the evaluated PFAS, PFOA, PFOS, PFDA, and GenX were associated with higher toxicity exposure risks. For the identified key concern PFAS, it is necessary to simplify detection techniques, promote targeted large-scale safe treatment technologies, and explore intelligent monitoring tools to reduce regulatory lag, thereby effectively monitoring, preventing, and controlling PFAS contamination.

The wet oxidation of pharmaceutical sludge for the treatment and production of value-added materials was investigated. The experiments were carried out in a stainless-steel autoclave reactor with chemical synthetic pharmaceutical sludge. The highest removal rate of total suspended solids (90.1%) and volatile suspended solids (98.4%) was achieved at 260 °C for 60 min with an initial oxygen pressure of 0.8 MPa. Simultaneously, the total chemical oxygen demand removal rate (78.7%) and the soluble chemical oxygen demand removal rate (81.6%) were obtained. The volatile fatty acid concentration—including acetic acid, propanoic acid, isobutyric acid and isovaleric acid—increased to 4819 mg/L with pH 12.56, which indicated the possibility of improving the quality of wet oxidized sludge solution as a potential carbon source by adding reagents. Scanning electron microscopy images showed that the sludge became a loose porous structure after wet oxidation, which is beneficial for dewatering performance. Energy dispersive spectroscopy images illustrate that carbon elements in sludge migrate from solid to liquid phases during the wet oxidation process. These results provide meaningful data for the design of further works and demonstrate that wet oxidation is a promising method for the treatment of pharmaceutical sludge, and the produced volatile fatty acids, including acetic acid and propanoic acid, are potential carbon sources for the biological treatment of wastewater.

Emerging pollutants such as microplastics in water environments readily accumulate microorganisms on their surfaces, forming biofilms and concentrating antibiotic-resistant bacteria (ARB) and antibiotic resistance genes (ARGs). Consequently, microplastic biofilms have attracted the attention of researchers. Horizontal gene transfer (HGT) of ARGs is one of the primary ways that bacteria acquire antibiotic resistance. Most studies focus on the effects of nanomaterials on suspended bacteria, but microplastic biofilms as hotspots for horizontal gene transfer also warrant significant investigation. This study primarily explored and compared the effects of nano-titanium dioxide on the conjugation transfer frequency of ARGs in suspended bacteria and microplastic biofilms. Nano-titanium dioxide could promote ARG conjugation in both suspended bacteria and microplastic biofilms, with a greater effect on the former. The mechanism involved nano-titanium dioxide promoting the production of reactive oxygen species (ROS) in suspended and biofilm bacteria, increasing the synthesis of outer membrane proteins, enhancing the cell membrane permeability, and elevating the expression levels of conjugation-related genes, thereby facilitating the conjugation transfer of ARGs. Biofilm bacteria, being heavily encased and protected by extracellular polymeric substances (EPS), exhibit greater resistance to external environmental pressure, resulting in the weaker impact of nano-titanium dioxide on biofilm bacteria compared to suspended bacteria. This study reveals the risk of ARG conjugation transfer within microplastic biofilms induced by nanomaterials, providing valuable insights into the risks of microplastic and antibiotic resistance dissemination in water environments.

The treatment of antibiotic mycelial residue (AMR) has emerged as a critical challenge hindering the sustainable development of the biopharmaceutical industry. As a representative hazardous solid waste generated during antibiotic manufacturing processes, AMR may pose substantial risks to environmental safety. This review elucidates the properties and hazards of AMR while systematically reviewing current mainstream treatment technologies. Building upon the elucidation of underlying mechanisms, it further examines the application bottlenecks and research progress associated with different techniques. Through a comprehensive understanding of existing research achievements, this paper proposes future development strategies and perspectives for AMR treatment, highlighting that integrated multi-technology treatment approaches may represent the predominant developmental direction in this field.

To reveal the nature of CO₂ reduction to formate with high efficiency by in situ hydrogen produced from hydrothermal reactions with iron, DFT calculations were used. A reaction pathway was proposed in which the formate was produced through the key intermediate species, namely iron hydride, produced in situ in the process of hydrogen gas production. In the in situ hydrogenation of CO₂, the charge of H in the iron hydride was −0.135, and the Fe–H bond distance was approximately 1.537 Å. A C-H bond was formed as a transition state during the attack of H^δ− on C^δ+. Finally, a HCOO species was formed. The distance of the C-H bond was 1.107 Å. The calculated free energy barrier was 16.43 kcal/mol. This study may provide new insight into CO₂ reduction to formate in hydrothermal reactions with metal.