Search Results (276)

To meet the demand for ultra-high-purity arsenic (≥7N) from crude arsenic (As ≥ 99.3%, Sb ≤ 0.6%), an integrated process combining chlorination, distillation and hydrogen reduction was developed. After preliminary purification of crude arsenic by vacuum distillation, chlorine was applied to convert arsenic and its impurities into chlorides. Low-boiling chlorides such as SbCl₃, S₂Cl₂ and Se₂Cl₂ were separated by distillation, and ultra-pure AsCl₃ was finally reduced by hydrogen to obtain ultra-high-purity arsenic. Under optimal conditions—10 mL·min⁻¹ Cl₂ flow, 20 mm–30 mm arsenic particle size and 80 mm–90 mm packing height—the chlorine utilization reached 92.3%. Distillation at 433 K with 4 h total reflux and a 5:1 volumetric reflux ratio yielded AsCl₃ of 99.99999% purity, with S and Se below 0.02 ppm and 0.01 ppm, respectively. Hydrogen reduction at 1123 K, H₂/AsCl₃ molar ratio 1.8 and 623 K condensation temperature achieved an arsenic recovery of 99.13%, a chlorine residue of 20 ppb and a final arsenic purity of 99.9999%. This study provides a feasible route for large-scale production of high-purity arsenic. Full article

The widespread use of antibiotics has led to the persistence of antibiotic-resistant bacteria (ARB) and antibiotic resistance genes (ARGs) in drinking water systems, posing potential public health risks at the point of use. In this study, a residential secondary water supply system (SWSS) in eastern China was investigated over one year to characterize microbial communities, ARB and ARG occurrence, and their associations with water quality in bulk water and biofilms. Culture-based methods, flow cytometry, quantitative PCR, and high-throughput 16S rRNA and ITS sequencing were applied. Although conventional treatment removed 94.8% of total bacteria, significant microbial regrowth occurred during secondary distribution, with the highest heterotrophic plate counts observed in rooftop storage tanks (up to 4718 CFU/mL). ARG concentrations increased along the distribution line, and the class 1 integron intI1 was enriched in downstream locations, indicating enhanced horizontal gene transfer potential. Sulfonamide resistance genes dominated the resistome, accounting for more than 60% of total ARG abundance in water samples. Seasonally, ARG levels were higher in autumn and winter, coinciding with elevated disinfectant residuals and lower temperatures. Chlorine was negatively associated with total bacterial abundance, while positive correlations were observed with the relative abundance of several ARGs when normalized to bacterial biomass, suggesting selective pressure under oxidative stress. Turbidity and bacterial abundance were positively correlated with ARB, particularly sulfonamide-resistant bacteria. Biofilms exhibited more stable microbial communities and provided microhabitats that facilitated microbial persistence. Notably, fungal abundance showed strong positive correlations with multiple ARGs, implying that microbial interactions may indirectly contribute to ARG persistence in SWSSs. These findings highlight the role of secondary distribution conditions, disinfectant pressure, and microbial interactions in shaping resistance risks in residential water supply systems, and provide insights for improving microbial risk management at the point of consumption. Full article

This study systematically analyzed the pollution levels, distribution characteristics, and associated health risks of 17 organochlorine pesticides (OCPs) and 9 polychlorinated biphenyls (PCBs) in Oviductus Ranae (Rana dybowskii) from major production areas in Heilongjiang Province, China. OCPs and PCBs were detected in all samples. The total concentration of OCPs ranged from 11.7 to 67.9 ng/g (dry weight), while that of total PCBs ranged from 4.43 to 8.06 ng/g. Endosulfans constituted the predominant OCP group, accounting for 54.5% of ∑OCPs, with an α/β-endosulfan ratio (~2:1) indicative of recent agricultural input. Among DDTs, the dominance of p,p′-DDE and the absence of parent DDT suggested aerobic degradation of historical residues. For HCHs, the isomer profile (β-HCH predominance, α/γ-HCH = 0.27) pointed to weathered lindane sources. The PCB profile was uniquely dominated by lower-chlorinated congeners (PCB1 and PCB29), implying influences from atmospheric transport and/or in situ microbial dechlorination of legacy PCBs. The persistent organic pollutants (POPs) contamination profile in Oviductus Ranae reflects a combined influence of recent pesticide application, weathered historical residues, and long-range transport. Although the concentrations are below current regulatory limits, the cumulative and persistent nature of these POPs, coupled with the product’s medicinal use, justifies a precautionary stance regarding long-term consumption. The distinct congener patterns underscore the necessity for future research to prioritize the environmental behavior and toxicology of dominant transformation products within such specific agro-ecosystems. Full article

This study evaluated the clinical bactericidal efficacy and safety of a novel chlorine dioxide teat disinfectant compared to a traditional iodine glycerin disinfectant in dairy cows. The randomized controlled trial included long-term natural exposure (100 cows) and teat surface disinfection (40 cows) experiments. Key metrics assessed were somatic cell count (SCC), teat skin health (dryness, roughness, hyperkeratosis), and bacterial reduction rates against Staphylococcus aureus, Escherichia coli, and Streptococcus spp. Results demonstrated that the chlorine dioxide teat disinfectant achieved comparable to iodine glycerin disinfectant in controlling the rate of SCC exceeding the threhold (3.57% vs. 4.50% at day 10; p > 0.05), teat skin dryness, end roughness, and hyperkeratosis severity showed no significant differences over time or between iodine glycerin (control) and chlorine dioxide teat disinfectant groups (all p > 0.05). Notably, quantitative bacteriological assessment revealed significantly higher log₁₀ reduction values for chlorine dioxide teat disinfectant (2.14) versus iodine glycerin controls (1.93; p < 0.05). Microbiological evaluation further demonstrated complete pathogen eradication (100.00%) by chlorine dioxide across all isolates (S. aureus, E. coli, Streptococcus spp.), whereas iodine glycerin achieved 99.84–100.00% bactericidal rates. The findings suggest that chlorine dioxide teat disinfectant is a sustainable and effective alternative to iodine glycerin disinfectant, offering robust antimicrobial activity, improved teat condition, and reduced residue concerns. Further multicenter studies are warranted to validate these outcomes under diverse herd management conditions. Full article

The removal of residual free chlorine ions from industrial wastewater is a critical step toward achieving sustainable and environmentally compliant water reuse. Excess chlorine in sludge collector water causes corrosion of process equipment, inhibits biological treatment, and leads to toxic discharge effects. In this study, an intelligent control strategy was developed for an ion-exchange-based dechlorination process to dynamically regulate chlorine concentration in the effluent stream. A pilot-scale ion-exchange filtration unit, designed with a nominal capacity of 500 L h⁻¹, was constructed using a strong-base anion-exchange resin to selectively adsorb chloride and free chlorine ions. A total of 200 experimental observations were obtained to characterize the nonlinear relationship between inlet flow rate and outlet chlorine concentration under varying operational conditions. Based on these experimental data, an Adaptive Neuro-Fuzzy Inference System (ANFIS) model was developed in MATLABR2025 to simulate and control the ion-exchange process. Two model-optimization techniques, Grid Partition + Hybrid and Subtractive Clustering + Hybrid, were applied. The subtractive clustering approach demonstrated faster convergence and superior accuracy, achieving RMSE = 0.147 mg L⁻¹, MAE = 0.101 mg L⁻¹, and R² = 0.993, outperforming the grid-partition model (RMSE ≈ 0.29, R² ≈ 0.97). The resulting ANFIS model was subsequently integrated into a MATLAB/Simulink-based intelligent control system for real-time regulation of chlorine concentration. A comparative dynamic simulation was performed between the proposed ANFIS controller and a conventional PID (Proportional-Differential-Integral) controller. The results revealed that the ANFIS controller achieved a faster response (rise time ≈ 28 s), lower overshoot (≈6%), and shorter settling time (≈90 s) compared to the PID controller (rise time ≈ 35 s, overshoot ≈ 18%, settling time ≈ 120 s). These improvements demonstrate the ability of the proposed model to adapt to nonlinear process behavior and to maintain stable operation under varying flow conditions. Full article

This study evaluates an integrated approach for recovering lead and silver from lead cake through chlorination roasting followed by acid leaching. The lead cake originates from sulfuric acid leaching of zinc ferrite residues obtained during the hydrometallurgical processing of zinc calcine. The effects of roasting temperature, lead cake-to-NaCl mass ratio, and roasting duration on metal recovery were systematically examined to determine optimal process conditions. Based on the experimental results, roasting at 550 °C for 1.5 h with a lead cake-to-NaCl mass ratio of 1:3, followed by leaching in 1 M HCl, was selected as a representative and sufficiently effective condition for the combined process. Under these conditions, nearly complete dissolution of Pb and Ag was achieved, reducing their contents in the final solid residue to 0.90% and 0.0027%, respectively. Compared to direct chloride leaching, the combined process provided higher extraction efficiencies (Pb 98.67%, Ag 98.09%) and a lower final residue mass (34% vs. 45%). The roasting step enables the solid-state conversion of PbSO₄ into highly soluble chloride phases (PbCl₂ and Pb(OH)Cl), while ZnFe₂O₄, Fe₂O₃ and SiO₂ remain stable and form the inert matrix of the residue. Acid leaching at a lower solid-to-liquid ratio (1:10) ensures near-complete dissolution of Pb and Ag, whereas aqueous leaching at a high ratio (1:100) results in incomplete Pb removal. The compliance leaching test (EN 12457-2) confirmed that the residue produced after the optimized two-step treatment meets the EU criteria for inert waste. Overall, the proposed combined process enhances Pb and Ag recovery, minimizes environmental risk, and offers a technically robust and sustainable route for treating lead-containing industrial residues. Full article

Rhenium is one of the rarest and most strategically important metals, indispensable in high-temperature superalloys and platinum–rhenium catalysts used across the aerospace and petrochemical industries. Owing to its limited primary reserves, recovering rhenium from secondary sources, such as spent catalysts, superalloy residues, and metallurgical dusts, has become vital to ensuring supply security. This review examines technological developments between 1998 and 2025, focusing on how operational parameters, including temperature, leaching time, reagent concentration, and solid-to-liquid ratio, govern dissolution kinetics and overall process efficiency. Comparative evaluation of hydrometallurgical, alkaline, and hybrid processes indicates that modern systems can achieve recovery rates exceeding 98% through selective oxidation, alkaline activation, or combined pyro and hydrometallurgical mechanisms. Acid–chlorine leaching facilitates rapid, low-temperature dissolution; alkaline sintering stabilises rhenium as soluble perrhenates; and hybrid smelting routes enable the concurrent separation of rhenium and osmium. Sustainable aqueous systems employing nitric and ammonium media have also demonstrated near-complete recovery at ambient temperature under closed-loop recycling conditions. Collectively, these findings highlight a technological transition from energy-intensive, acid-based pathways towards low-impact, recyclable, and digitally optimised hydrometallurgical processes. The integration of selective oxidants, phase engineering, circular reagent management, and artificial intelligence-assisted modelling is defining the next generation of rhenium recovery, combining high extraction yields with reduced environmental impact and alignment with global sustainability goals. Full article

The catalytic mechanism of the Zn(II)-dependent chlorothalonil dehalogenase from Pseudomonas sp. CTN-3 (Chd) was examined using molecular dynamics (MD) simulations, Bayesian network analysis, and Markov state model analysis to quantify its motions. Chd selectively substitutes an aromatic chlorine-carbon bond in chlorothalonil (TPN; 2,4,5,6-tetrachloroisophtalonitrile) with an aromatic alcohol (4-hydroxytrichloro-isophthalonitrile; 4-OH-TPN). It is a homodimer with two solvent-accessible channels in each monomer, which are proposed to provide different routes for substrate and products to access/leave the catalytic Zn(II) site. Based on MD simulations, Chd exhibits allosteric behavior wherein a “Y”-shaped substrate channel exhibits a “flip flop” mechanism, where the “right” substrate channel opens to allow TPN to enter, after which it closes, followed by the “left” channel opening. The “right” channel then reopens, likely to allow the product, 4-OH-TPN, to leave the active site, but this reopening of the right channel drives the “left” channel to close. Coupled with the substrate channels alternately opening and closing, a corresponding possible Cl⁻ channel opens and closes. Although the dynamics of this process are fast, Chd needs to overcome a 5 kT free-energy barrier for this transition and to relax after opening. Additionally, exposed “wing” residues, hydrophilic residues at the ends of protruding α-helices, act as allosteric indicators, signaling the complex allosteric motions required to open the substrate channel. We propose, for the first time, a dynamic mechanism that drives substrate binding and product release, providing new insight into Chd’s catalytic mechanism. Full article

The study explores γ-valerolactone (GVL) pulps as a sustainable approach to producing microfibrillated (MFC) and nanofibrillated (NFC) cellulose from sugarcane bagasse, a widely available agro-industrial by-product. Pulp was obtained by acid-catalyzed organosolv delignification with a GVL–water system. MFC was generated through a simple disc refiner, while NFC was produced by TEMPO-mediated oxidation followed by mechanical treatment in a colloidal mill. NFC and MFC produced using the same methodology from a commercial sugarcane totally chlorine-free (TCF) soda–anthraquinone (soda–AQ) pulp served as a reference. Structural and physicochemical characterization involved optical transmittance, turbidity, conductimetry, X-ray diffraction, viscosity, FTIR, carboxyl content, cationic demand, degree of polymerization, and morphology by scanning electron microscopy (SEM). Results demonstrated that xylan and residual lignin contents influenced MFC formation, and the NFC showed properties comparable to those of the commercial pulp with fewer fibrillation passes. The study highlights GVL pulping as a greener, efficient alternative to conventional processes, opening new pathways for producing viscosity-controlled nanocellulose suspensions suitable for advanced applications. Full article

The persistence of organochlorine pesticides, such as Aldrin and Dieldrin, in water bodies worldwide necessitates the development of efficient Advanced Oxidation Processes (AOPs) for water treatment or remediation. However, comparative studies evaluating the performance of distinct plasma discharge geometries against acoustic cavitation for the mineralization of these specific chlorinated cyclodienes remain scarce. This study investigates the comparative efficacy of four non-thermal technologies, ultrasound, dielectric barrier discharge (DBD) plasma, glow discharge plasma, and corona discharge plasma, for the simultaneous degradation of Aldrin and Dieldrin in a model contaminated aqueous solution (5 μg/L). All experiments followed a 3²-factorial design, and the residual concentrations of these pesticides were quantified by GC-MS after Solid-Phase Microextraction (SPME). All four methods achieved high degradation efficiencies, ranging from 92.5% to 100% for Aldrin and 92.6% to 99.2% for Dieldrin. Corona discharge plasma achieved the highest performance, resulting in 100% removal of Aldrin. However, ultrasound proved to be the most advantageous, achieving a 98% removal efficiency for both pesticides under its mildest conditions (3125 W/L ultrasonic power density for 3 min). The study confirmed that while Aldrin is highly susceptible to these technologies, Dieldrin remains the limiting factor for regulatory compliance. Chemical analysis did not conclusively identify any organic degradation by-products, suggesting that these AOPs may promote complete mineralization of the pollutants. Full article

Intermittent water supply is common in Palestine, prompting schools to rely on on-site water storage systems, including underground and roof tanks. Prolonged and uncontrolled water storage leads to quality degradation, especially with free residual chlorine (FRC) depletion. Hence, this poses health risks to students and staff. This pilot (field) study evaluated the effectiveness of booster chlorination under the current storage conditions to optimize and improve the existing chlorination process. Four schools were selected based on the type of water storage systems (two with underground tanks, two with roof tanks) and building age. Booster chlorination was applied at two chlorine doses (0.5 mg/L and 1 mg/L). FRC was monitored until levels dropped below 0.05 mg/L. Results show that the currently applied chlorine dose (0.5 mg/L) is insufficient to reach the minimum national FRC standard (0.2 mg/L) after 30 min. In contrast, a 1 mg/L chlorine dose is more effective in maintaining the minimum FRC concentration limit for a longer time. In addition, manual mixing is ineffective in large underground tanks, while it is effective in roof tanks. This study urges the need to revise the national chlorination guidelines and to adjust chlorination practices to ensure safe drinking water in schools. Full article

This study investigated a plasma-sonic treatment that combines plasma-activated water (PAW) and ultrasound (US) as an alternative to conventional sodium hypochlorite (NaOCl), which may leave harmful chlorine residues and generate toxic by-products in fresh produce. The treatment was applied to kale to evaluate its decontamination efficiency and storage stability during 7 days at 4 °C. PAW was generated at 52 W and 14.4 kHz for 624 s, and US was applied at 20 kHz and 250 W for 624 s. The plasma-sonic treatment achieved microbial inactivation of indigenous bacteria by 3.2 log CFU/g, which is comparable to the 3.0 log CFU/g reduction achieved by NaOCl treatment. Moreover, the plasma-sonic treatment group exhibited the highest initial moisture content (89.42%) and maintained higher firmness during storage than the NaOCl-washed and untreated groups. Collectively, these findings indicate that the combined PAW and US washing method constitutes a promising non-chlorine-based intervention that enhances microbial stability while maintaining the physicochemical quality of fresh leafy vegetables. Full article

Background: Hospitals generate large volumes of single-use plastic waste, which are predominantly incinerated. To improve sustainability, standardized procedure-specific surgical trays have been implemented, reducing waste and setup time. This early feasibility study investigated whether all residual plastics from surgical procedures could be recycled via pyrolysis into high-quality oil for circular reuse in medical supply production. Methods: All residual plastics from five transurethral resection (TUR) trays were subjected to pyrolysis at 430–460 °C in a batch reactor. Condensable fractions were separated into heavy (HF) and light (LF) oils, while non-condensable gases and coke were quantified. Chemical analyses included the density, water content, heating value, and elemental composition. Results: From 1.102 kg of input material, the process yielded 78 weight percent (wt%) oil (HF 59.1%, LF 40.9%), 20.5 wt% gas, and 1.5 wt% coke. HF solidified at room temperature, whereas LF remained liquid, reflecting distinct hydrocarbon chain distributions. The oils exhibited densities of 767.0 kg/m³ (HF) and 748.9 kg/m³ (LF), heating values of 46.39–46.80 MJ/kg, low water contents (<0.05 wt%), and minimal contamination (silicone ≤ 193 mg/kg; chlorine ≤ 110 mg/kg). Conclusions: Pyrolysis of surgical tray plastics produces decontaminated high-energy oils comparable in quality to fossil fuels, with a material recovery rate exceeding 75% and potential CO₂ savings of ~ 2.9 ton per t plastic compared with incineration. This process provides a technically and ecologically viable pathway toward a scalable circular economy in healthcare. Full article

This study investigates the torrefaction of polyvinyl chloride (PVC) and cellulose, two major constituents of agricultural waste, with the aim of improving chlorine removal and enhancing the energy quality of the resulting solid products. Thermodynamic simulations using HSC Chemistry 9.0 were first conducted to predict equilibrium compositions, particularly chlorine-containing species. Thermogravimetric analysis (TGA) and coupled TGA-FTIR were employed to monitor mass loss and identify gaseous chlorine compounds. Based on these preliminary results, torrefaction experiments were carried out at temperatures of 250–300 °C and durations of 30–90 min. The results demonstrate a significant synergistic effect between cellulose and PVC during co-torrefaction, achieving 97% chlorine removal under optimal conditions (9:1 cellulose-to-PVC ratio, 250 °C, 30 min). This effective dechlorination helps mitigate Cl-induced corrosion and reduces the risk of dioxin formation in industrial applications, enabling the sustainable upcycling of PVC-contaminated biomass into clean solid fuels. Torrefaction temperature exerted a stronger influence than time on mass loss, yielding approximately 40% solid residue at 300 °C. While both solid and energy yields decreased with increasing temperature and time, the O/C and H/C atomic ratios decreased by 56% and 48%, respectively, indicating a substantial improvement in fuel properties. The observed synergy is attributed to cellulose-derived hydroxyl radicals promoting PVC dehydrochlorination. This process offers a scalable and economically viable pretreatment route for PVC-containing biomass, potentially reducing boiler corrosion and hazardous emissions. Full article

Small rural water utilities in the Appalachia region of the US often experience extreme water loss while struggling to maintain water quality compliance. This study quantifies the impact of reducing water loss on distribution system water quality in Martin County, Kentucky. Hydraulic and water quality models were developed, calibrated, and validated using EPANET for chlorine residuals and KYPIPE for trihalomethane (TTHM) formation. The models evaluated water loss reduction scenarios ranging from the current 70% to the industry target of 15%. Results showed that lowering water loss increased residence times, causing chlorine residual declines of 22–68%, with one site falling to the 0.2 mg/L threshold. TTHM concentrations increased by 12–18% in winter–spring and 26–44% in summer–fall, with two sites exceeding the individual 0.080 mg/L maximum contaminant level. These novel findings indicate that reducing water loss can unintentionally degrade water quality, underscoring the need for integrated planning. Recommended mitigation strategies include seasonal operational adjustments, water source and TTHM precursor management, optimized tank management, targeted flushing, and phased infrastructure upgrades. The modeling framework developed offers potential for broader application in other rural systems facing similar challenges. Full article