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To oxidize trace concentrations of organic contaminants under conditions relevant to surface- and groundwater, air-diffusion cathodes were coupled to stainless-steel cathodes that convert atmospheric O2 into hydrogen peroxide (H2O2), which then was activated to produce hydroxyl radicals (·OH). By separating H2O2 generation from its activation and employing a flow-through electrode consisting of stainless-steel fibers, the two processes could be operated efficiently in a manner that overcame mass-transfer limitations for O2, H2O2, and trace organic contaminants. The flexibility resulting from separate control of the two processes made it possible to avoid both the accumulation of excess H2O2 and the energy losses that take place after H2O2 has been depleted. The decrease in treatment efficacy occurring in the presence of natural organic matter was substantially lower than that typically observed in homogeneous advanced oxidation processes. Experiments conducted with ionized and neutral compounds indicated that electrostatic repulsion prevented negatively charged ·OH scavengers from interfering with the oxidation of neutral contaminants. Energy consumption by the dual-cathode system was lower than values reported for other technologies intended for small-scale drinking water treatment systems. The coordinated operation of these two cathodes has the potential to provide a practical, inexpensive way for point-of-use drinking water treatment.

Dichloramine (NHCl2) naturally exists in reverse osmosis (RO) permeate due to its application as an antifouling chemical in membrane-based potable reuse treatment. This study investigated mechanisms of background NHCl2 hydrolysis associated with the generation of oxidative radical species in RO permeate, established a kinetic model to predict the oxidative capacity, and examined its removal efficiency on trace organic contaminants in potable reuse. Results showed that NHCl2 hydrolysis generated transient peroxynitrite (ONOO-) and subsequently dissociated into hydroxyl radical (HO•). The maximal HO• exposure was observed at an RO permeate pH of 8.4, higher than that from typical ultraviolet (UV)-based advanced oxidation processes. The HO• exposure during NHCl2 hydrolysis also peaked at a NH2Cl-to-NHCl2 molar ratio of 1:1. The oxidative capacity rapidly degraded 1,4-dioxane, carbamazepine, atenolol, and sulfamethoxazole in RO permeate. Furthermore, background elevated carbonate in fresh RO permeate can convert HO• to carbonate radical (CO3•-). Aeration of the RO permeate removed total carbonate, significantly increased HO• exposure, and enhanced the degradation kinetics of trace organic contaminants. The kinetic model of NHCl2 hydrolysis predicted well the degradation of contaminants in RO permeate. This study provides new mechanistic insights into NHCl2 hydrolysis that contributes to the oxidative degradation of trace organic contaminants in potable reuse systems.

UNLABELLED: Wastewater treatment plants (WWTPs) are indispensable biotechnology facilities for modern cities and play an essential role in modern urban infrastructure by employing microorganisms to remove pollutants in wastewater, thus protecting public health and the environment. This study conducted a 13-month bacterial community survey of six full-scale WWTPs in Hong Kong with samples of influent, activated sludge (AS), and effluent to explore their synchronism and asynchronism of bacterial community. Besides, we compared AS results of six Hong Kong WWTPs with data from 1,186 AS amplicon data in 269 global WWTPs and a 9-year metagenomic sequencing survey of a Hong Kong WWTP. Our results showed the compositions of bacterial communities varied and the bacterial community structure of AS had obvious differences across Hong Kong WWTPs. The co-occurrence analysis identified 40 pairs of relationships that existed among Hong Kong WWTPs to show solid associations between two species and stochastic processes took large proportions for the bacterial community assembly of six WWTPs. The abundance and distribution of the functional bacteria in worldwide and Hong Kong WWTPs were examined and compared, and we found that ammonia-oxidizing bacteria had more diversity than nitrite-oxidizing bacteria. Besides, Hong Kong WWTPs could make great contributions to the genome mining of microbial dark matter in the global wanted list. Operational parameters had important effects on OTUs abundance, such as the temperature to the genera of Tetrasphaera, Gordonia and Nitrospira. All these results obtained from this study can deepen our understanding of the microbial ecology in WWTPs and provide foundations for further studies. IMPORTANCE: Wastewater treatment plants (WWTPs) are an indispensable component of modern cities, as they can remove pollutants in wastewater to prevent anthropogenic activities. Activated sludge (AS) is a fundamental wastewater treatment process and it harbors a highly complex microbial community that forms the main components and contains functional groups. Unveiling who is there is a long-term goal of the research on AS microbiology. High-throughput sequencing provides insights into the inventory diversity of microbial communities to an unprecedented level of detail. At present, the analysis of communities in WWTPs usually comes from a specific WWTP and lacks comparisons and verification among different WWTPs. The wide-scale and long-term sampling project and research in this study could help us evaluate the AS community more accurately to find the similarities and different results for different WWTPs in Hong Kong and other regions of the world.

The advanced in situ oxidation polymerization technique was employed to synthesize the SiNWs@PANI composite material, which exhibited a unique hybrid structure displaying remarkable properties. The optimized polyaniline content of 5% significantly enhanced the photocatalytic performance of SiNWs@PANI, surpassing pure SiNWs in degradation efficiency. A comprehensive study explored the photocatalytic mechanisms of SiNWs@PANI, focusing on environmental factors such as catalyst composite content, pollutant nature, and solution pH. The material exhibited exceptional activity in the photocatalytic degradation of ciprofloxacin, achieving a remarkable degradation efficiency of up to 91.54% at a concentration of 10 mg L−1. Our findings revealed a significant dependency of degradation efficiency on solution pH, with alkaline conditions favoring enhanced catalytic activity. A rigorous derivation experiment identified the final degradation product, corroborating the effectiveness of SiNWs@PANI in ciprofloxacin degradation and providing insights into the underlying photocatalytic processes. This work offers a novel perspective and methodology for developing highly efficient and environmentally friendly photocatalytic materials, with promising implications for water treatment and environmental remediation applications. [ABSTRACT FROM AUTHOR]

Rapid industrialization and ever‐increasing global population culminate in continuous upsurge in freshwater crisis worldwide. The most reliable and promising solution to this crisis is utilizing sea‐water as the freshwater source, and desalination technologies pave the way for efficient production of freshwater from sea‐water. In this regard, membrane‐based desalination method comes forth owing to its' efficient separation, operational ease, and low‐energy consumption. Metal–organic frameworks (MOFs), the most explored crystalline porous materials, show tremendous promise as membrane‐materials for desalination owing to their structural diversity, tunability, and porous voids which provide secondary water channels. Given significant advances are made in MOF‐materials for desalination in the past few years, it is crucial to systematically summarize the recent progress and development of this field. In this review, a brief overview of various saline water systems and prerequisites for desalination are first presented. Then, advanced fabrication strategies MOF‐membranes followed by the recent progress in MOF‐materials for various desalination processes such as reverse osmosis and forward osmosis are systematically summarized. Finally, the authors' perspectives on the unsolved scientific and technical challenges and opportunities for MOF‐integrated membranes toward real‐world implementation are proposed. With further systematic development, MOF‐materials promise to provide an ideal platform for next‐generation desalination technology. [ABSTRACT FROM AUTHOR]

Organic pollutants in water pose significant challenges for water treatment due to their harmful effects and resistance to conventional methods. The rapid increase in industrial wastewater discharge has heightened the need for effective pollutant degradation techniques. Photo‐Fenton technology, an advanced oxidation process, has gained attention for its ability to degrade a wide range of organic contaminants in water. Developing high‐performance photo‐Fenton catalysts is therefore crucial. Graphitic carbon nitride (g‐C3N4) stands out in this field due to its suitable energy band structure, stable properties, and simple synthesis process. However, its application is limited by a low specific surface area, narrow light absorption, and high recombination rate of photogenerated carriers. This review provides a concise overview of current research on g‐C3N4 in photo‐Fenton technology, covering synthesis methods, modifications, and the mechanisms enhancing its photo‐Fenton activity. It also highlights key factors affecting g‐C3N4's effectiveness in photo‐Fenton reactions and discusses recent advancements in its applications. The review concludes with an analysis of existing challenges and potential future directions for g‐C3N4‐based photo‐Fenton catalysts, offering theoretical insights to advance their industrial use in wastewater treatment. [ABSTRACT FROM AUTHOR]

Carbon aerogels (CAs) have garnered significant attention due to their multifunctional applications. Biomass waste, abundantly generated by agriculture and industry, serves as a primary carbon source. However, developing a facile, sustainable, and efficient method to produce CAs from biomass waste remains challenging. In this study, a one‐step Zn2+ ion‐glue‐assisted carbonization technique was developed to produce large‐scale, high‐performance CAs. Various biomass materials (wood bits, peanut shells, bamboo bits, and straw waste) were treated in a molten salt system (ZnCl2/KCl) at 300 °C for 2 h to obtain large‐block CAs derived from biomass bits. Zn2+ ions cleave cellulose hydrogen bonds in natural biomass, facilitating the dehydration crosslinking reaction among cellulose, hemicellulose, and lignin, thus reconstructing the entire block structure. The resulting CAs exhibited high porosity (95 %) and low density (0.078 g/cm3). Numerous hydroxyl and carbonyl groups were preserved during the low‐temperature treatment, facilitating chemical modification for diverse applications. For instance, amidoxime functionalized CAs were utilized as filters for selective and highly efficient extraction of U(VI) from wastewater. The adsorption capacity and extraction efficiency reached 801.2 mg/g and 95 % with a flux rate of 6.1×103 L/m2 ⋅ h. [ABSTRACT FROM AUTHOR]

In this study, hydrothermally synthesized magnesium oxide demonstrated effective fluoride adsorption, with a maximum capacity of 199.67 mg g−1 and equilibrium was achieved within 60 min. The morphology of magnesium oxide and the adsorption mechanism were investigated by SEM, FTIR, BET and XPS. The adsorption process conformed to the Freundlich isotherm and pseudo-second-order kinetic models. The ΔH and ΔS of fluoride adsorption by this material were 44.58 kJ mol−1 and 163.31 J mol−1 K−1, respectively, indicating surface heterogeneity and specific adsorption kinetics. Optimal fluoride removal was observed in the pH range of 4–11, with the highest adsorption capacity achieved at pH 5.0. Co-existing ions significantly influenced the adsorption performance (Cl− < NO3− < SO42− < HCO3− < PO43−). These findings underscore the potential application of magnesium oxide in water treatment and suggest avenues for further optimization of synthesis and operational parameters. [ABSTRACT FROM AUTHOR]

Sub-10 µm microplastics (MPs) in aquatic environments pose significant ecological and health risks due to their mobility and potential to carry harmful microcontaminants. Our effluent analysis from a Hong Kong Sewage Treatment Works shows that traditional treatment often fails to effectively remove these MPs. These small-sized MPs are commonly neglected due to challenges in accurate quantification, analysis, and removal. This study introduces a nanobubble-assisted flotation process that enhances the removal efficiency of both regular and irregular small-sized MPs from wastewater. The proposed process outperforms the traditional flotation process by fostering a more effective interaction between bubbles and MPs, increasing removal rates of MPs from 1 µm to 10 µm by up to 12% and providing a total efficiency boost of up to 17% for various particle sizes. Improvements are attributed to enhanced collision and adhesion probabilities, hydrophobic interactions, as well as better floc flotation. Supported by empirical evidence, mathematical models, and Molecular Dynamics simulations, this research elucidates the nanoscale mechanisms at play. The findings confirm the nanobubble-assisted flotation technique as an innovative and practical approach to removing sub-10 µm MPs in water treatment processes. Sub-10 µm microplastic pose severe environmental risks. Here, authors introduce an advanced nanobubble assisted flotation technique that enhances microplastic removal, providing a promising solution for effective water treatment. [ABSTRACT FROM AUTHOR]

Graphitic carbon nitride (g‐C3N4) assisted photocatalytic production of hydrogen peroxide (H2O2 has already attracted the interest of many researchers due to its environmental sustainability. Nevertheless, the inherent drawbacks of g‐C3N4 limit its progress. Metal‐free modification strategies, including nanostructure design, defect introduction, doping, and heterojunction construction, have been developed to improve the efficiency of g‐C3N4 photocatalytic H2O2 production. Compared to metal modification, metal‐free strategies avoid the use of precious metals and the leaching of heavy metal ions, which have the advantages of good stability and environmental friendliness. However, a comprehensive review of H2O2 production from g‐C3N4 modified by metal‐free strategies is still lacking. This review first recaps the mechanism of photocatalytic H2O2 production by g‐C3N4, including photoexcitation, carrier separation and redox reactions. Then, the perspective advances in metal‐free modified g‐C3N4 photocatalysts are presented, with the special focus on the kernel connection between different strategies and mechanism based on the pivotal stages of H2O2 production. Subsequently, recent applications of g‐C3N4‐based photocatalysts for in situ generated H2O2, mainly including water purification and organic synthesis, are briefly discussed. Finally, the prospects of g‐C3N4‐based photocatalysts are envisioned with the hope that it will have "something to do" in the field of H2O2 production. [ABSTRACT FROM AUTHOR]

Recycling organic waste and water treatment residues in nanoform is a promising technology in various farming systems, and its effect on aggregate stability, biological activity, and canola production in degraded soils is largely unknown. Hence, we evaluated the effect of nano-biochar (nB) and nano-water treatment residues (nWTR) at levels 50, 100, and 250 mg kg−1 as compared to soil without amendments on the aggregate stability, biological activity, and canola yield in degraded soil. The results showed that the structure coefficient (SC) values are higher when nB and nWTR are added at 100 mg kg−1 soil than at levels 50 and 250 mg kg−1. In our study, the high aggregate stability in the soil treated with nB and nWTR is likely due to their higher content of nutrients, organic carbon, clay, and CEC. The seed weight of the canola plant increased with increasing nB by more than 64%, while it decreased with increasing nWTR. Microbial biomass carbon (MBC) and the activity of dehydrogenase (DHA) and catalase (CLA) increased significantly in the treated pots with the addition of nB and nWTR at various rates. The results of the pot experiment recommended that the applications of nWTR and nB could be used as a promising strategy to improve soil quality and crop yield while also increasing the recycled efficiency of WTR and rice straw. [ABSTRACT FROM AUTHOR]

Highlights With the emergence of two‐dimensional (2D) materials analogous to graphene, transition metal carbides and carbonitrides with unique desirable characteristics known as MXenes have turned out to be a hot research topic. Recent studies increasingly focus on the structure–property relationships of MXenes and their hybrid formations with other materials. The exfoliation and delamination of MXenes using various agents is gaining attention, while their application in functional composites presents another exciting research direction. However, the exfoliation of multi‐layered MXene into few‐layered nanosheets using bio‐based agents remains underexplored. In this study, tannic acid (TA) is employed as a bio‐exfoliating agent to delaminate Ti3C2Tx MXene, while optimizing the ratio of TA to achieve efficient exfoliation and dye adsorption. The MXene/TA composites demonstrated a maximum adsorption capacity of 187.264 mg/g and a removal efficiency of 93.69% for methylene blue (MB) in water, in accordance with the Langmuir isotherm model. Furthermore, MB adsorption caused MXene to coagulate into floccules, enabling easy removal via filtration. The study highlights the trifold role of tannic acid in MXene as a delaminating, antimicrobial, and adsorption‐enhancing agent, creating a multifunctional MXene‐tannic acid system. It introduces a new class of hybrid materials with effective applications in water purification. Additionally, incorporating this hybrid material into polymers can fine‐tune their properties, leveraging the synergistic effects of the trio to develop high‐performance smart polymer composites for diverse applications. Synthesis of MXene from Ti3C2Tx Optimization of the delamination efficiency of the biomolecule tannic acid Characterization of tannic acid‐MXene delaminated composites Analysis of the antibacterial efficiency of tannic acid delaminated MXene Investigation of water purification efficiency of delaminated MXene [ABSTRACT FROM AUTHOR]

This review investigates the pervasive issue of dye effluent pollution in African surface waters, focusing on its significant adverse effects on both human health and environmental quality. Drawing from 63 articles published between 2004 and 2022, the review includes studies from Northern, Western, Eastern, Central, and Southern Africa, illustrating the widespread nature of dye contamination across the continent. Five primary sources of dye effluents are identified: textiles, food industries, dye producers, artisan dyes, and tannery-paint industries, all of which contribute substantially to the degradation of water quality. The physicochemical properties of dye effluents show high toxicity levels in surface waters, with significant regional variations. These variations highlight the importance of considering the specific characteristics of dye types and processing chemicals to fully understand the contamination levels. In evaluating treatment methods, the review finds that adsorption, coagulation/flocculation, filtration, and advanced oxidation processes (AOPs) such as photocatalysis, photo-Fenton oxidation, and plasma-chemical treatment are effective in mitigating dye pollution. The application of these methods varies across different African regions, indicating the need for region-specific approaches based on local conditions and available resources. The review also examines the impact of dye effluents on aquatic ecosystems and human health, with risk assessments revealing effects ranging from acute to chronic. This demonstrates the urgent need for targeted interventions to address dye effluent pollution in African surface waters, thereby protecting both environmental and public health. Highlights: Dye effluent pollution severely impacts human health and the environment, particularly in African surface waters. Six key industries contribute to dye pollution in Africa: textile, food, pharmaceutical, tannery, paint, and artisanal. Effective treatment methods like adsorption, filtration, and AOPs show promise but require larger-scale implementation [ABSTRACT FROM AUTHOR]

Textile wastewater poses a significant environmental challenge, primarily due to the presence of diverse contaminants, especially textile dyes. Untreated release of these effluents directly into aquatic systems can lead to esthetic degradation, eutrophication, reduced photosynthetic activity, and accumulation of hazardous substances. Although conventional treatment methods are employed for reducing the contaminant load in effluents, they often are less efficient, thus prompting the exploration of innovative alternatives. Current review highlights myco-remediation as an inexpensive, promising and environmentally sustainable solution. Fungi, with their diverse decontamination mechanisms such as biosorption, biotransformation, and immobilization, prove effective in reducing heavy metals, persistent organic pollutants, and emerging contaminant levels present in these effluents, However, more research effort is needed to apply the biodegradation strategy to decompose completely the "forever chemicals" per‐ and polyfluorinated alkyl substances. Fungi play a key role in degrading and decolorizing textile dyes due to their biocatalytic activity mediated by the production of oxidative enzymes, such as laccases, lignin peroxidases, and manganese peroxidases, as well as their dye adsorption capabilities. This comprehensive review concentrates on fungi-based remediation of textile wastewater effluents, including the mechanisms they employ. While most studies concentrate on effluent treatment, this review also explores the concurrent utilization of biomass and growth kinetics for efficient reduction in pollutant concentrations. Further, the current work showed data on optimization of growth conditions such as pH, temperature and nutrient requirements that lead to efficient effluent decontamination. [ABSTRACT FROM AUTHOR]

Vascular tubules in natural leaves form quasi-fractal networks that can be metallized. Traditional metallization techniques for these lignocellulose structures are complex, involving metal sputtering, nanoparticle solutions, or multiple chemical pretreatments. Here we present a novel, facile, and reliable method for metallizing leaf-derived lignocellulose scaffolds using silver microparticles. The method achieves properties on-par with the state-of-the-art, such as broadband optical transmittance of over 80%, sheet resistances below 1 Ω/sq., and a current-carrying capacity exceeding 6 A over a 2.5 × 2.5 cm² quasi-fractal electrode. We also demonstrate copper electrodeposition as a cost-effective approach towards fabricating such conductive, biomimetic quasi-fractals. Additionally, we show that these metallized structures can effectively eliminate pathogenic microorganisms like fecal coliforms and E. coli, which are bacterial indicators of microbiological contamination of water. We finally show that these oligodynamic properties can be significantly enhanced with a small externally applied voltage, indicating the noteworthy potential of such structures for water purification and pollution control. [ABSTRACT FROM AUTHOR]

Freshwater purification from wasted water and seawater is crucial in addressing the global problem of water scarcity. Porous fiber felt with a micro/nanostructure emerges as an efficient approach for water purification; however, its production usually relies on chemical postprocessing to create micro/nano structures on the fiber surface, which might pollute the environment. This study proposed an ecofriendly method to produce micro/nanostructured copper fiber felt without chemical treatment. First, a new transverse-feeding vibration cutting is proposed to fabricate micro/nanostructured fibers with controllable structure characteristics. Through the sintering of the structured fibers without postprocessing, the fiber felt can be produced in an ecofriendly way and exhibit special wettability and excellent photothermal properties. Felt-based freshwater purification, including oil–water separation and solar-driven seawater desalination, can be realized effectively. Results show an oil–water separation efficiency of > 90% and a high evaporation rate of water of > 1.08 kg m−2 h−1 at 73 mW cm−2 are achieved, demonstrating the application prospect of the produced fiber felt. Highlights: A transverse-feeding vibration cutting process is proposed to fabricate micro/nanostructured copper fibers. Micro/nanostructured based felts can achieve special wettability and corresponding wettability transition. Micro/nanostructured fibers can enhance the felts' photothermal conversion ability and reduce heat transfer loss. [ABSTRACT FROM AUTHOR]

Industrial dye effluent causes significant risks to the environment. The present study was focused on photocatalytic degradation of the dye Direct Red 28 using a ternary composite of graphitic carbon nitride, TiO2, and polyorthoanisidine (g-C3N4/TiO2/ POA), prepared by in-situ oxidative polymerization o-anisidine. The synthesized composite g-C3N4/TiO2/POA properties were characterized using different analytical techniques. X-ray diffraction (XRD) results revealed the prominent pattern of TiO2 and g-C3N4 in the composite peak at 2θ° while Fourier transform infrared (FTIR) results provided the confirmation peaks for g-C3N4/TiO2/POA and POA at 1,110 cm-1 and 1,084 cm-1 for C-O-C ether. Scanning electron microscopy (SEM) demonstrated an increase in the average size of the composite up to 428 nm. The energy-dispersive X-ray spectroscopy (EDX) spectrum provided the weight percentages of the C, O, and Ti in the composite were 8.5%, 45.69%, and 45.81%, respectively. The photocatalytic degradation of Direct Red 28 dye under UV irradiation using a composite showed that 86% Direct Red 28 dye was degraded by a 30 mg/L dose of g-C3N4/TiO2/POA in 240 min at pH 2. After four consecutive cycles, the utilized composite showed 79% degradation of Direct Red 28, demonstrating the stability and effectiveness of the g-C3N4/TiO2/POA photocatalyst. The high reusability and efficiency of the g-C3N4/TiO2/POA composite are due to increased light absorption range and reduced e-/h+ recombination rate in the presence of g-C3N4 and POA. [ABSTRACT FROM AUTHOR]

Abstract\nSTATEMENT OF NOVELTYRemoval of Cd(II) and Pb(II) from aqueous solutions is a challenging task and the search for novel adsorbents is underway. This study examined the efficiency of nanobiochar (NB) and rice husk (RH) in the adsorption and removal of Cd(II) and Pb(II) from water. The effect of various physicochemical parameters such as initial pH, initial Cd and Pb concentration, adsorbent dosage, and contact time were tested. SEM/EDX images confirmed the adsorption of Pb and Cd with surface physical and chemical changes. The maximum Pb removal was noted at pH 6 using NB (96%) and at pH 8 for RH (90%), and the maximum Cd removal by NB was recorded at 8 pH (91%) and by RH at pH 6 (87%). The decline in adsorption intensity at lower pH suggested protonation of the adsorbent surface causing cation-cation repulsion. Most of the adsorption occurred within the initial 60 min. A continuous gradual increase in the adsorption with time suggested multilayer formation. Of the three isotherms, the Freundlich model fits the present data best, implying an infinite surface coverage and indicating the potential for multilayer adsorption of Pb and Cd on the surfaces of RH and NB adsorbents. In conclusion, this study highlights the promising potential of NB as a cost-effective adsorbent for the removal of Cd and Pb ions from aqueous solutions.This study explores the effectiveness of utilizing low-cost natural and agricultural waste biomasses for removing Cd(II) and Pb(II) ions from aqueous solutions. [ABSTRACT FROM AUTHOR]

Inspired by the intelligent gel phase transition effect, we applied temperature-responsive γ-FeOOH/KGM(Ga)/PNIPAM hydrogel with reversible sol-gel transition for uranium enrichment and separation in carbonate-containing wastewater. In carbonate-containing wastewater, the hydrogel achieved a high uranium removal rate of 92.3%, exceeding 90% even in actual uranium mine wastewater. Additionally, the adsorption-reduction-nucleation-crystallization mechanism of uranium on the temperature-responsive hydrogel was revealed using multi-spectral coupling techniques. [Display omitted] Exploiting the intelligent photocatalysts capable of phase separation provides a promising solution to the removal of uranium, which is expected to solve the difficulty in separation and the poor selectivity of traditional photocatalysts in carbonate-containing uranium wastewater. In this paper, the γ-FeOOH/konjac glucomannan grafted with phenolic hydroxyl groups/poly- N -isopropylacrylamide (γ-FeOOH/KGM(Ga)/PNIPAM) thermosensitive hydrogel is proposed as the photocatalysts for extracting uranium from carbonate-containing uranium wastewater. The dynamic phase transformation is demonstrated to confirm the arbitrary transition of γ-FeOOH/KGM(Ga)/PNIPAM thermosensitive hydrogel from a dispersed state with a high specific surface area at low temperatures to a stable aggregated state at high temperatures. Notably, the γ-FeOOH/KGM(Ga)/PNIPAM thermosensitive hydrogel achieves a remarkably high rate of 92.3% in the removal of uranium from the wastewater containing carbonates and maintains the efficiency of uranium removal from uranium mine wastewater at over 90%. Relying on electron spin resonance and free radical capture experiment, we reveal the adsorption-reduction-nucleation-crystallization mechanism of uranium on γ-FeOOH/KGM(Ga)/PNIPAM thermosensitive hydrogel. Overall, this strategy provides a promising solution to treating uranium-contaminated wastewater, showing a massive potential in water purification. [ABSTRACT FROM AUTHOR]

AbstractSeedlings of 95 greenhouse-grown interior Douglas-fir half-sibling families originating from four breeding zones were subject to overwatering and periodic underwatering and compared to an optimally watered control (15 per family = 1425 seedlings total). Averaged over all trees, annual height was reduced by 4% and 11% compared to controls for overwatering and periodic underwatering, respectively. Family overwatered seedling height was 135–75%, and underwatered height was 100–75% of their respective control heights. Shorter families under stress grew like their control compared to taller families, but this was reversed in taller families when the watering conditions were ideal. A survival analysis indicated that after 30–50 days without water, family survival varied from 25% to 90%, and most trees died after 60 days. The breeding zone had little effect on the tolerance to suboptimal water or survival during complete water withdrawal and did not interact with watering treatments. Family traits for tolerance to overwatering favoured root biomass, traits for underwatering favoured reduced stem biomass, especially in ratio to roots, and traits for survival favoured belowground biomass over aboveground biomass. No tradeoffs between tolerance to over- and underwatering were found. Some families did well in all three conditions and some in one or the other. The study results suggest that variation in family growth and survival to suboptimal watering partly relate to root and stem biomass partitioning in the interior Douglas-fir population of British Columbia. [ABSTRACT FROM AUTHOR]

The current work was designed to eliminate reactive yellow 18 dye (RY‐18) via adsorption from water, and CO2 from the gas stream, using the tragacanth gum‐based Cr doped NiO N.P.s/Clay (GCNC) composite. The one‐pot synthesis approach was used to produce the adsorbent, and physical and chemical properties were assessed using techniques like XRD, FTIR, UV‐visible spectroscopy, SEM, DLS, Zeta Potential, and adsorption–desorption isotherm. The GCNC composite demonstrated an impressive adsorption potential and percentage removal of 398 mg/g and 91.28%, respectively. Temkin and intraparticle diffusion models with R2 values of 0.98401 and 0.99918 were the most effective at fitting the experimental adsorption model. The thermodynamics parameters, including the change in enthalpy (H), entropy (S), and Gibbs free energy (G), demonstrated the endothermic and spontaneous nature of the adsorption process. A positive H value indicates an endothermic process, while a negative G value indicates a spontaneous process. According to the isotherms fitting model, the capacity for adsorbing CO2 at 25 °C and 1 atm was 4.8 mmol/g. The significant correlation between the slope in the log‐linear plot of the isosteric heat of adsorption and CO2 adsorption performance indicates that the isosteric heat of adsorption can be used as a predictive tool for CO2 adsorption performance. These significant results underscore the potential of the GCNC composite to revolutionize the water treatment field and CO2 capture, offering hope for a more sustainable and cleaner future. [ABSTRACT FROM AUTHOR]

Sludge thickening is a fundamental stage of treatment. This study investigated the application, in continuous treatment, of polymeric bubbles produced with cationic polymer P2900 and cocamidopropyl betaine (CAPB), a zwitterionic surfactant. The proposed reagent combination aims to form aerated flakes, solid waste structures, and rapidly rising air bubbles, ideal for treatments in compact units. Using this combination, it was possible to achieve a total solids concentration of 45% with the modified bubbles and 25% with the conventional water treatment. This level of thickening occurred under the following operating conditions: initial total solids (TS) concentration of 10 g L−1, a flow rate of 5 L min−1, saturation pressure (psat) of 3 atm, and polymer dosage of 10 mg (gTS)−1. The suggested mechanism of action involves the adhesion of P2900 molecules to CAPB at the air/water interface, forming a lining on the bubble surface. Additionally, polymerized species form due to the residual aluminum (Al) in the sludge, which would occur during flocculation in the helical tubular flocculator (HTF), adsorbing the micelles and bubbles of CAPB. The critical micellar concentration (CMC) of CAPB was 0.26 mmol L−1. Polymeric bubble technology can provide an efficient and cost-effective approach to sludge thickening in continuous treatment. [ABSTRACT FROM AUTHOR]

Functional nanocomposite materials are hybrid systems combining nanoscale fillers with a matrix, resulting in enhanced properties such as mechanical strength, thermal stability, and electrical conductivity. These materials are highly versatile, finding applications across a broad range of fields, including aerospace for lightweight, strong components, electronics for flexible and high-performance devices, healthcare for targeted drug delivery and tissue engineering, and environmental sectors for water purification and pollutant sensing. Their tunable properties make them ideal for addressing emerging challenges in various industries. This special issue entitled as "Functional Nanocomposite Materials" of Journal of Materials Science is a remarkable collection of invited and contributed papers on this topic, showcasing outstanding recent research results in this field. [ABSTRACT FROM AUTHOR]

We demonstrate appropriate tuning of heterojunctions in CsPbBrxCl3−x−MoS2 composites (where x=0,1,2,3) by controlled regulation of the halide stoichiometry in the perovskite. A thorough optimization procedure determined the most effective photocatalyst, considering the pristine MoS2, perovskites with varying halide ratios, various physical mixing ratios of the two, and in‐situ synthesized composite ratios of CsPbBrxCl3−x and MoS2 (2 : 1, 1.5 : 1, 1 : 1, 1 : 1.5, 1 : 2). Under two hours of exposure to visible light, a remarkable photocatalytic performance of CsPbBrCl2 : MoS2 with a 1 : 2 ratio was observed, removing 98 % of the methylene blue (MB) dye. Notably, only the CsPbBrCl2 and MoS2 composite demonstrated higher efficiencies since it resulted in a n‐n type II heterojunction. Additionally, the CsPbBrCl2 : MoS2 composite exhibits the highest reaction rate constant, fifteen times higher than the pristine perovskite. Reusability assessment of this combination revealed sustained activity of 87 % for up to 5 cycles. The hydrogen evolution reaction investigations were carried out using the optimized CsPbBrCl2 : MoS2 composite, which yielded 265 times more hydrogen than pristine CsPbBrCl2. The Faradaic efficiency for 1 : 2 CsPbBrCl2 : MoS2 was found to be 96.61 %. Our results offer crucial perspectives on optimizing perovskite‐MoS2 composites and demonstrate their utility in sustainable applications, including water treatment, renewable energy harvesting, and environmental remediation. [ABSTRACT FROM AUTHOR]

Thermoelectric (TE) materials have attracted significant attention because they can be used to directly harvest waste heat into electricity. Organic TE materials like poly(3,4‐ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) have advantages including high mechanical flexibility, low cost, and low intrinsic thermal conductivity. However, their TE properties are notably inferior to their inorganic counterparts. Here, PEDOT:PSS films with very high thermoelectric properties through the sequential treatments with H2SO4, water, and ethanol solution of tetrakis(dimethylamino)ethylene (TDAE) are reported for the first time. The PEDOT:PSS films can exhibit a Seebeck coefficient of 58.2 µV K−1 and electrical conductivity of 1552 S cm−1, and the corresponding power factor is 526 µW m−1 K−2. The water treatment prior to the TDAE solution treatment is crucial for the high TE properties of PEDOT:PSS films. Without the water treatment, the control PEDOT:PSS films exhibit a Seebeck coefficient of only 32.4 µV K−1 and electrical conductivity of 1124 S cm−1, and the corresponding power factor is only 118 µW m−1 K−2. The effect of the water treatment on the Seebeck coefficient is attributed to the swelling of PEDOT:PSS films, which facilitates the penetration of TDAE from solution into the polymer films and thus the reduction of PEDOT:PSS. [ABSTRACT FROM AUTHOR]

This study envisages the utilization of unique properties of Gd2S3 and 2D graphitic carbon nitride towards the development of novel multiutility water treatment nanomaterial. The g-C3N4/Gd2S3 as a novel nanomaterial with desirably tuned properties was characterized by standard techniques, like PXRD, SEM, UV-visible spectroscopy, and energy dispersive X-ray spectroscopy (EDX), to thoroughly analyze the synthesized material. The observed results signify synergism of individual properties of pristine constituents on g-C3N4/Gd2S3 composite formation adding suitability towards the electrochemical sensing and photocatalytic applications. The g-C3N4/Gd2S3 nanocomposite material was optimized for electrochemical detection of dopamine (DA). Electrochemical studies with composite modified glassy carbon electrode under neutral pH conditions indicated good sensitivity over an optimum operational range, paving the way for potential applications in dopamine sensing. Differential pulse voltammetry (DPV) results demonstrated a linear concentration range spanning from 0.5 to 200 μM, with the lowest (1.2 nM) limit of detection. The desired modulation of photocatalytic descriptors (band gap, recombination rate, charge carrier concentration, and flat band potentials) on composite formation were utilized in visible light degradation of methylene blue and rhodamine B as representative contaminants. The g-C3N4/Gd2S3 nanocomposite exhibited favorable qualities of environmentally viable operational conditions, catalytic reproducibility, stability, and selectivity, highlighting its potential for real-time application. [ABSTRACT FROM AUTHOR]

Valorizing biodegradable raw materials derived from agri‐waste is ecologically beneficial. Employing such materials to produce adsorbents is a smart platform for applications in wastewater purification. Lignin is one of the most plentiful natural biopolymers in the world. Its macromolecular structure possesses phenolic and carboxyl groups that can capture heavy metals and dyes. Lignin can be chemically and physically modified to generate adsorbent materials with enhanced capacity to remove pollutants from wastewater. In this work, lignin has been used as a natural resource to synthesize metal oxide‐based nanoadsorbents. The synthesized lignin‐based green nanomaterials effectively removed common pollutants from wastewater including dyes, heavy metals, and bacteria. The lignin‐based water purification technique holds immense potential to effectively remove the most common pollutants from wastewater. [ABSTRACT FROM AUTHOR]

Ni@C nanowires were in situ grown with about 5 nm nickel particles uniformly distributed along the one-dimensional framework. By assembling into a membrane, Ni@C exhibited 95.7% solar spectral absorption and a high water interfacial evaporation rate of 2.38 kg m−2 h−1 under one sun. Superhydrophobic modification further enabled long-term stable saline water evaporation. This work demonstrates the promising potential of non-precious Ni for solar photothermal conversion applications. [ABSTRACT FROM AUTHOR]

A significant share of wastewater produced during different processes is released to the surroundings without further treatment. Therefore, polluted water sources are triggering diseases like typhoid. To avoid this, various techniques have been developed for the removal of contaminants from the water. Iron-copper bimetallic nanoparticles (NPs) supported on the reduced graphene oxide (rGOFeCu) were prepared which showed excellent antibacterial activity, efficient dechlorination of 1,1,1-trichloroethane (TCA), and removal of methylene blue (MB). The characterization of prepared nanocomposites was done by transmission electron microscopy (TEM) and X-ray diffraction (XRD). Iron-based bimetallic NPs supported on the graphene were successfully synthesized as confirmed by TEM. Iron has a strong antibacterial effect on microorganisms, especially bacteria. We conducted the antibacterial activity of different compositions of nanocomposite toward Escherichia coli to understand the efficacy of prepared nanocomposites. In the same time and concentration conditions, rGOFeCu showed the best antibacterial activity, as compared to the graphene-based iron. Results show that the excellent antibacterial activity was exhibited by using rGO-Fe95Cu05 within two hours. More than 98% of cell inhibition was observed. The further increase in copper loading has no major effect on antibacterial activity. rGO-Fe95Cu05 exhibited excellent removal efficiency of TCA (99%) within 30 min as compared to other compositions of FeCu. It was found that rGO-Fe95Cu05 exhibited excellent removal efficiency against degradation of methylene blue (MB) through activation of sodium percarbonate (SPC). The results indicated that more than 99% of MB was removed within 15 min. The rGOFeCu represented a great potential material for antibacterial activity towards E. coli and remediation of other pollutants in the wastewater such as TCA and removal of MB. [ABSTRACT FROM AUTHOR]

Gallium and indium, metals present in light-emitting diode (LED) lighting technology, can be effectively recovered from aqueous solutions by sorption. For this purpose, carbonaceous materials, such as activated carbon, or low-cost biosorbents as beer bagasse, spent coffee grounds or peanut shells, and a low-cost zeolite as chabazite, were characterized by BET, FTIR, XRD, and SEM analysis prior use. Protonated chabazite, with high surface area (505 m2/g) and a Si/Al molar ratio of 3.4, showed high sorption capacities for gallium (56 mg/g) and indium (92 mg/g), which is 10 to 30 times higher than those of our carbonaceous materials (T = 298 K, pH < 3, dosage = 1 g/L). Sorption experiments with both metals in solution showed a competitive effect between gallium and indium for the sorption sites of the chabazite, showing more affinity toward gallium than indium. Ga3+sorbed/In3+sorbed molar ratio above 2 was achieved for the same initial concentration of both metals, increasing to almost 3 when the initial gallium concentration increased, which was appropriate since gallium concentration tends to be higher in LED chips. However, the sorption capacity for both metals was always around 0.35 mmol Ga + In/g. The selectivity of the chabazite was conditioned by different behavior of both metals in aqueous solution at the sorption pH (below 3.5) being the predominant species in solution Ga(OH)2+ for gallium and In3+ for indium. Sorption with protonated chabazite can be used in the treatment of spent LEDs leachate for the dual purpose of water purification and selective metal separation. [ABSTRACT FROM AUTHOR]

Two physical treatments (heat via water bath and cold air) with various temperatures (20/70/75/80°C and - 80/-90°C) and exposure times (20, 30, 40 s) were carried out to identify a decontaminating effect on zoonotic pathogens on broiler carcasses. Subsequently, carcasses were analyzed for thermotolerant Campylobacter (C.), Salmonella, Escherichia (E.). coli and total colony count (TCC). Moreover, for the hot water treatment, qPCR with viable/dead differentiation (v-qPCR) was applied to detect viable but non-culturable cells (VBNC) of Campylobacter, referred to as intact but putatively infectious units (IPIU). Hot water immersion was tested on carcasses inoculated with C. jejuni and Salmonella, while cold air treatment was evaluated for naturally contaminated carcasses of broiler flocks colonized with Campylobacter. For hot water treatment, the statistically significant reducing effect was about 1 log10 CFU/ml for both Salmonella and Campylobacter for 70-80°C and 20/30 s treatments. The effect of heat treatment for Campylobacter was smaller when samples were analyzed with v-qPCR with reductions of 0.5-0.8 log10 IPIU/ml in mean. Cold air treatments at -90°C were effective in reducing the mean contamination level of Campylobacter by 0.4-0.5 log10 CFU/ml at all exposure times (p < 0.05). Hot water treatments showed a decreasing trend on TCC by 0.6-0.9 log10 CFU/ml (p < 0.05). TCC counts were not significantly affected by cold air treatment. For E. coli no statistically significant reductions were observed by hot water treatment. The cold air treatment at -90°C for 20 and 40 s led to a reduction of E. coli by 0.4 and 0.8 log10 CFU/ml (p < 0.05), respectively. Treatment of carcasses with higher bacterial levels tended to show higher reduction. The research demonstrated that the efficacy of physical treatments for decontamination of broiler carcasses was more pronounced for hot water immersion than for cold air exposure. In conclusion, the results shed light on the potential application of these physical treatments in practice to reduce the quantitative load of contaminating pathogens to enhance food safety in the broiler meat production. [ABSTRACT FROM AUTHOR]

Capacitive deionization techniques are of interest in water treatment technology due to their low cost, excellent efficiency, and environmental friendliness. Currently, metal–organic frameworks are highly impactful candidates for use as electrode materials in electrochemistry. It provides a large pore volume, good chemical stability, and a high specific surface area. Tuning metal–organic frameworks with carbon materials will have a good impact on electrode materials with increasing performance. This study shows a facile and effective strategy for arranging flow capacitive desalination technology for salt removal. The conducting network of Fe-MOF/CNTs provides rapid electron transport and offers a high diffusion length of ions. This material exhibited excellent desalination performance, with a high salt adsorption of 80.575 mg/g at 1.6 V at an initial NaCl concentration of 1000 mg/L. Overall, the facile method and fabrication strategy greatly advances water treatment applications. Highlights: Fe-MOF/CNT composites were obtained by a one-step hydrothermal process for improved CDI performance The strategy endowed the material with excellent porosity, and the presence of iron oxidation sites improved the overall conductivity of the electrode. • Fe-MOF/CNTs were used as flow electrodes for novel capacitive deionization • Fe-MOF/CNTs exhibited a high NaCl electrosorption capacity of 80.575 mg/g. Our strategy provides matching properties and an excellent combination of Fe-MOF and CNTs for improved CDI performance. [ABSTRACT FROM AUTHOR]

Nanofiltration (NF) membranes are commonly supplied in spiral-wound modules, resulting in numerous drawbacks for practical applications (e.g., high operating pressure/pressure drop/costs). Vacuum-driven NF could be a promising and low-cost alternative by utilizing simple components and operating under an ultra-low vacuum pressure (<1 bar). Nevertheless, existing commercial membranes are incapable of achieving practically relevant water flux in such a system. Herein, we fabricated a silk-based membrane with a crumpled and defect-free rejection layer, showing water permeance of 96.2 ± 10 L m−2 h−1 bar−1 and a Na2SO4 rejection of 96.0 ± 0.6% under cross-flow filtration mode. In a vacuum-driven system, the membrane demonstrates a water flux of 56.8 ± 7.1 L m−2 h−1 at a suction pressure of 0.9 bar and high removal rate against various contaminants. Through analysis, silk-based ultra-permeable membranes may offer close to 80% reduction in specific energy consumption and greenhouse gas emissions compared to a commercial benchmark, holding great promise for advancing a more energy-efficient and greener water treatment process and paving the avenue for practical application in real industrial settings. Vacuum-driven nanofiltration (NF) is a promising and low-cost alternative to pressure driven NF but existing commercial membranes currently not achieve any relevant water flux in such a system. Here, the authors fabricate a silk-based membrane with a crumpled and defect-free rejection layer, showing high flux and salt rejection rate under cross-flow filtration mode. [ABSTRACT FROM AUTHOR]

This work studies the kinetic model for the solar-driven fabrication of CoWO4/NCW heterostructure photocatalysts and investigates their enhanced photocatalytic degradation activity. The synthesis of CoWO4/NCW, its characterization, and the kinetic aspects of photocatalytic degradation under solar light. New nanocomposite prepared from Nano cellulose (NCW) by hydrolysis cotton waste (CW) by nitric acid and cobalt tungstate (CoWO4) prepared from sodium tungstate and cobalt chloride by wet chemical method and characterized through XRD, FTIR, EDX, and FE-SEM analyses. The composite's performance in organic oxidation from refinery wastewater (RWW) was evaluated under solar light. The high removal ratio was 97.4% for organic pollutants (OP) in refinery wastewater. The results indicate that the heterostructure exhibits improved photocatalytic performance compared to individual components, which kinetics model was the best to represent the photocatalytic degradation of organic pollutants from oily wastewater over the heterostructure CoWO4/NCW catalyst. Add future applications of this finding in the relevant industries. [ABSTRACT FROM AUTHOR]

Carbon Quantum Dots (CQDs) are nanoscale carbon‐based particles with unique quantum properties. Because of their customizable size, optical properties, and surface functions, CQDs are frequently used in a wide range of applications. The present thorough analysis delves into the crucial function of CQDs in the photocatalytic breakdown of Methylene Blue (MB), providing valuable perspectives on their production, attributes, and catalytic processes. The effects of pH, wavelength, intensity, and other variables on the effectiveness of MB degradation are covered in detail. An analytical review of the kinetic models used to estimate the deterioration process is given. For improved stability and recyclability, the synergistic effects of CQD‐based composites and developments in catalyst immobilization techniques are examined. Prospects for the future center on reactor designs, integration into large‐scale water treatment systems, and optimization of CQD features. The research highlights the revolutionary potential of CQDs in transforming wastewater treatment and advancing environmentally sound solutions. [ABSTRACT FROM AUTHOR]

In order to solve problems such as low pollutant concentrations, large treatment volumes and high purification costs in tailwater treatment of recirculating aquaculture systems, a new renewable biomass ash filter material was developed to remove nitrogen and phosphorus from tailwater, which is environment-friendly, economical and highly effective. Properties of biomass ash filter materials produced under different conditions were studied through orthogonal experiments with sintering temperature, keeping time and material trapped time as factors and the main control factors affecting the properties of filter materials were obtained. The pore evolution and forming principle of the filter material during the sintering process can be inferred by characterizing and analyzing the structural characteristics and microscopic morphology of biomass ash filter materials produced at different sintering temperatures. This helps to clarify the performance control mechanism of these filter materials via their different structures. Based on this, the biomass ash filter material that has the best performance could be selected as a test group. And commercial filter materials including biochar, ceramic granules and natural zeolite were used as control groups to conduct phosphate and nitrite adsorption tests to evaluate the adsorption performance of the biomass ash filter material. The results show that sintering temperature is the main control factor affecting the properties of biomass ash filter materials. As the sintering temperature increases, wollastonite, melilite and anorthite phases are generated sequentially in the filter materials, which leads to a series of microstructure transformations, such as crystallization, vitrification and precipitation. This is the reason for the formation of the different pore structures. In this process, water pores in the filter materials are gradually converted into closed pores. This causes positive effects of high sintering temperature on stomatal porosity, total porosity, and compressive strength. It also brings negative effects of high sintering temperature on permeable porosity, water pore rate, water absorption and permeability, pH and EC values. The performance control mechanism of these filter materials exists because of the two contrary effects. Without aging, the biomass ash filter material produced by sintering at 1 170 ℃ for 40 minutes has better performance. This kind of filter material has a high saturation water absorption and average permeability rate, short water holding time, good formability and pore structure with a compressive strength of 0.74 MPa and total porosity of 65.49%. Its pH and EC values meet the demands of water purification. The unit adsorption capacity and removal rate of this filter material on phosphate can reach 0.996 mg/g and 2.767%, respectively. The phosphate adsorption effect is significantly better than that of biochar, ceramic granules and natural zeolite. The unit adsorption capacity and removal rate of this filter material on nitrite are 0.317 mg/g and 0.881%, respectively, which is equivalent to that of ceramic granules, significantly higher than natural zeolite and slightly inferior to biochar. The new renewable biomass ash filter material improves the defects of current mainstream filter materials for water purification. It is expected to meet the demand for nitrogen and phosphorus removal from circulating aquaculture tail water and can be used widely. [ABSTRACT FROM AUTHOR]

The need for sustainable, biodegradable materials to address environmental challenges, such as oil-water separation, is growing. Cellulose-based absorbents offer an eco-friendly alternative to synthetic materials. However, their hydrophobicity must be enhanced for efficient application. In this study, cellulose-based sorbents derived from Kraft and half-bleached chemo-thermomechanical pulp (BCTMP) were hydrophobized using silanization and alkyl ketene dimer (AKD) techniques. Hydrophobic properties were successfully imparted using methyltrimethoxysilane (MTMOS), n-octyltriethoxysilane (NTES), and N-(2-Aminoethyl)-3-aminopropyltrimethoxysilane (AATMS), with water contact angles ranging from 120° to 140°. The water sorption capacity was significantly reduced to below 1 g/g, whereas the oil sorption capacity remained high (19–28 g/g). The most substantial reduction in water vapor absorption (3–6%) was observed for the MTMOS- and AATMS-silanized samples. These results demonstrate the potential of hydrophobized cellulose-based sorbents as sustainable alternatives for oil-water separation, contributing to environmentally friendly water treatment solutions. [ABSTRACT FROM AUTHOR]

This study explored the synthesis of potash alum from disposed aluminum cans for water purification. The effect of the labels on the cans on the yield of alum was also investigated as it is economically beneficial for industry. Single crystals of potash alum were obtained and characterized by powder X-ray diffraction (P-XRD) and Fourier transform infrared (FTIR) spectroscopy. Through a series of jar test experiments, the characterized alum samples were used to purify river water samples. Some of the parameters investigated include; pH, turbidity, total suspended solids (TSS), total dissolved solids (TDS), electrical conductivity (EC) and chemical oxygen demand (COD). The results show that the alum samples were able to reduce the turbidity by 100 % and substantially decrease the TSS, TDS and COD over the five-hour period of study. However, there were slight increases in acidity and EC which could be corrected by other methods [ABSTRACT FROM AUTHOR]

Graphene oxide (GO) membranes have garnered significant attention in the field of membrane separation due to their superb hydrophilicity, abundant functional groups, extensive surface area, and chemical stability. In this study, we have established a simple and effective method to enhance GO layered materials using nitrogen-doped carbon dots (N–CDs) molecules as inserts and surface modifiers, aiming to develop highly efficient GO-based membranes. Consequently, the incorporation of N–CDs into the two-dimensional GO membrane augments its hydrophilicity and increases the membrane interlayer distance. Under ultra-low pressure nanofiltration conditions, the optimum GN-12 composite membrane exhibited a remarkable average pure water flux of 6.06 L m−2 h−1 bar−1. This flux was approximately 19.5 times higher than that of the pure GO membrane, which had a flux of 0.31 L m−2 h−1 bar−1. Furthermore, the composite membrane exhibited excellent capability in intercepting several charged dye molecules, with an interception rate exceeding 99.6%. Furthermore, the optimized composite membrane demonstrated robust performance and structural stability even under varying pH conditions. The findings of this fundamental research provide a straightforward and cost-effective strategy for the production of high-performance two-dimensional based nanofiltration membranes. [ABSTRACT FROM AUTHOR]

AbstractBackground: Obese adipose tissue produces various pro-inflammatory cytokines that are major contributors to adipose tissue inflammation.Objective: The present study aimed to determine the effects of HM-chromanone (HMC) against obesity and adipose tissue inflammation in high-fat diet-fed mice.Materials and methods: Twenty-four C57BL/6J male mice were divided into three groups: ND (normal diet), HFD (high-fat diet), and HFD + HMC. The ND group was fed a normal diet, whereas the HFD and HFD + HMC groups were fed a high-fat diet. After 10 weeks of feeding, the animals were orally administered the treatments daily for 9 weeks. The ND and HFD group received distilled water as treatment. The HFD+HMC group was treated with HM-chromaone (50 mg/kg).Results: HM-chromanone administration decreased body weight, fat mass, and adipocyte diameter. HM-chromanone also improved plasma lipid profiles, decreased leptin levels, and increased adiponectin levels. The inhibiting effect of HM-chromanone on SREBP-1c, PPARγ, C/EBPα, and FAS decreased adipogenesis, thereby alleviating lipid accumulation. Furthermore, HM-chromanone administration exhibited a reduction in macrophage infiltration and the expression of pro-inflammatory cytokines. HM-chromanone suppressed the phosphorylation of IκBα and NF-κB, leading to the inhibition of iNOS and COX2 expressions, resulting in decreased inflammation in adipose tissue.Discussion and conclusion: These results highlight the anti-obesity and anti-inflammatory properties of HM-chromanone, achieved through the downregulation of the SREBP-1c and NF-κB pathway in high-fat diet-fed mice. [ABSTRACT FROM AUTHOR]

Water contamination with metals poses significant environmental challenges. The occurrence of heavy metals (HMs) prompts modifications in plant structures, emphasizing the necessity of employing focused safeguarding measures. Cadmium (Cd), lead (Pb), and chromium (Cr) emerge as particularly menacing toxins due to their high accumulation potential. Increasing the availability of organic acids is crucial for optimizing toxic metal removal via phytoremediation. This constructed wetland system (CWs) was used to determine how oxalic acid (OA) treatments of textile wastewater (WW) effluents affected morpho-physiological characteristics, antioxidant enzyme activity, oxidative stress, and HM concentrations in Phragmites australis. Multiple treatments, comprising the application of OA at a concentration of 10 mM and WW at different dilutions (25%, 50%, 75%, and 100%), were employed, with three replications of each treatment. WW stress decreased chlorophyll and carotenoid content, and concurrently enhanced HMs adsorption and antioxidant enzyme activities. Furthermore, the application of WW was found to elevate oxidative stress levels, whereas the presence of OA concurrently mitigated this oxidative stress. Similarly, WW negatively affected soil-plant analysis development (SPAD) and the total soluble proteins (SP) in both roots and shoots. Conversely, these parameters showed improvement with OA treatments. P. australis showed the potential to enhance HM accumulation under 100% WW stress. Specifically, there is an increase in root SP ranging from 9% to 39%, an increase in shoot SP from 6% to 91%, and an elevation in SPAD values from 4% to 64% compared to their respective treatments lacking OA inclusion. The OA addition resulted in decreased EL contents in the root and shoot by 10%–19% and 13%–15%, MDA by 9%–14% and 9%–20%, and H2O2 by 14%–21% and 9%–17%, in comparison to the respective treatments without OA. Interestingly, the findings further revealed that the augmentation of OA also contributed to an increased accumulation of Cr, Cd, and Pb. Specifically, at 100% WW with OA (10 mM), the concentrations of Cr, Pb, and Cd in leaves rose by 164%, 447%, and 350%, in stems by 213%, 247%, and 219%, and in roots by 155%, 238%, and 195%, respectively. The chelating agent oxalic acid effectively alleviated plant toxicity induced by toxins. Overall, our findings demonstrate the remarkable tolerance of P. australis to elevated concentrations of WW stress, positioning it as an eco-friendly candidate for industrial effluent remediation. This plant exhibits efficacy in restoring contaminants present in textile effluents, and notably, oxalic acid emerges as a promising agent for the phytoextraction of HMs. KEY MESSAGE/HIGHLIGHTS: HMs stress decreased the physiology and morphology of Phragmites australis L. OA improved the photosynthetic pigments and antioxidant enzymes HMs accumulation and bioavailability increased under OA Phragmites australis L. showed higher efficacy for textile effluent treatment under OA NOVELTY: The adoption of ecological or nature-based approaches for treating textile industry wastewater poses significant challenges. Despite laboratory and field demonstrations showcasing the potential of macrophytes for remediating metal-polluted wastewater, this study investigates the Phragmites australis to address heavy metal contamination in wastewater. This research bridges this gap by presenting the outcomes of applying oxalic acid single and in combination with wastewater to Phragmites australis, focusing on the accumulation of cadmium, chromium, and lead from textile wastewater. [ABSTRACT FROM AUTHOR]

Removing toxic Pb(II) ions from aqueous solution by the peels of citrus reticulate (mandarin orange), a fruit industry waste, presents suitable scale-up possibilities. The Scanning Electron Microscope (SEM) and Brunauer-Emmett-Teller (BET) studies reflected that the mandarin orange peel powder had a porous surface area (32.46 m2g−1), average pore size and pore volume was 38.6 Å and 0.402 cm3g−1, respectively, favorable for binding Pb(II) ions. Fourier-transform infrared spectroscopy (FTIR) showed C-Br stretching, primary alcohol (C-O), phenolic O-H, and carbodimide N = C = N bands primarily helped to bind Pb(II) ions. The study evaluated and optimized the parametric influences of pH, adsorbate and biosorbent concentration, contact time and temperature on the removal efficiency of Pb(II) ions. A maximum of 97.08% Pb(II) was removed from 20 mg L−1 solution when 2.5 g L−1 adsorbent was present. The reaction obeyed the pseudo-second-order kinetic model. The intra-particle diffusion was involved in lead sorption. The Langmuir isotherm model resulted in an adsorption capacity of 23.04 mg g−1. 35.28% Pb(II) was removed in the 3rd adsorption-desorption cycle with 0.4 M HCl. The adsorption process was natural, impulsive and endothermic. The statistical investigation used Multiple Polynomial Regression (MPR) and Genetic Algorithm (GA). The analysis effectively forecasted the percentage removal at the optimized condition. NOVELTY STATEMENT: The results of toxic Pb(II) ion removal from aqueous solution by the peels of citrus reticulate (mandarin orange), a food industry waste, are reported. The maximum Pb(II) adsorption capacity of 23.04 mg/g. This work provides a new way to realize good adsorption capacity of Pb(II) by orange peel and accelerates to utilize for small and medium-sized industries in rural areas of 3rd World Countries. [ABSTRACT FROM AUTHOR]

Changes in the structure and properties of a microbial community of a sequencing batch reactor (SBR) enriched with phosphate-accumulating microorganisms (PAO) after a pH shift to more acidic values (pH 6.7‒7.1) were studied in. The relative abundance of Ca. Accumulibacter decreased from 43.6 to 13.9%, while abundance of potential PAO belonging to the genera Dechloromonas and Thauera increased. The overall share of PAO changed insignificantly (40‒43%). The share of glycogen-accumulating microorganisms (GAO), the main competitors of PAO, remained low throughout the experiment: abundance of the Competibacter 16S rRNA gene fragments before and after the pH shift was 2‒4%. While decrease in pH resulted in a drop in the amount of phosphates released during the anaerobic phase, the amount of phosphorus in the biomass (15‒17%) remained high, as well as phosphorus removal (92‒94%). [ABSTRACT FROM AUTHOR]

Desulfurization as a pre-treatment technique, of the transportation fuel is peremptory both for upgrading fuel quality for commercial exploitation and reducing the outflow of poisonous sulfur compounds for environmental remediation. This article encompasses the applications of mixed matrix membranes (MMMs) for the desulfurization of transportation fuels. This composite membrane system synergizes viable processability of the polymers and enhanced selectivity of different incorporated fillers. Hence it offers increased thermal stability, mechanical strength, excellent separation, and purification performance over traditional polymeric and inorganic membranes. These composite materials are widely studied for their potential applications in sensing, catalysis, water purification, gas separation, and adsorption. Herein, different types of MMMs with respect to fillers, chemical compositions and fabrication methods are focused and then systematically compiled and discussed the recent trend for the desulfurization of transportation fuels with profound scientific rationale. Finally, future prospects and room for further advancements in the wider spectrum of MMMs are discussed for better applications and adoptability in the processing of fuel oils. This review will assist the researchers working on the large-scale processing of transportation fuels with a single-point source of knowledge and will save ample amount of time as well as contribute into key future research directions. [ABSTRACT FROM AUTHOR]

The electro‐Fenton (EF) process is an advanced oxidation technology with significant potential; however, it is limited by two steps: generation and activation of H2O2. In contrast to the production of H2O2 via the electrochemical two‐electron oxygen reduction reaction (ORR), the electrochemical three‐electron (3e−) ORR can directly activate molecular oxygen to yield the hydroxyl radical (⋅OH), thus breaking through the conceptual and operational limitations of the traditional EF reaction. Therefore, the 3e− ORR is a vital process for efficiently producing ⋅OH in situ, thus charting a new path toward the development of green water‐treatment technologies. This review summarizes the characteristics and mechanisms of the 3e− ORR, focusing on the basic principles and latest progress in the in situ generation and efficient utilization of ⋅OH through the modulation of the reaction pathway, shedding light on the rational design of 3e− ORR catalysts, mechanistic exploration, and practical applications for water treatment. Finally, the future developments and challenges of efficient, stable, and large‐scale utilization of ⋅OH are discussed based on achieving optimal 3e− ORR regulation and the potential to combine it with other technologies. [ABSTRACT FROM AUTHOR]

Nanotechnology is an emerging branch of science that incorporates the nanomaterials recognized as nanoparticles ranging from 1–100 nm in size. This technology is being used in the food industry, pharmaceutical industry, agricultural industry, medical treatments, environmental science, biological research, and aquaculture industry. Increasing disease susceptibility, pathogenic emergence and divergence, less efficient vaccines, probiotics, and ineffective antibiotics forced us to seek an alternative approach to tackle these challenges. Nanotechnology can change our views, perceptions, and perspectives, as it has provided us with a necessary tool to address these challenges. This technology has revolutionized aspects of providing solutions to many hazardous issues like disease control, nutrient delivery, water purification, vaccines, and drug delivery in aquaculture using nanoparticles. Several nanoparticles have been used as growth promoters, e.g., zinc, iron, and selenium nanoparticles. Many of them have antibacterial properties, e.g., silver and copper nanoparticles. Besides that, these nanoparticles have few toxicological effects, when they are used without proper knowledge and lead to unrealistic results. Therefore, there should be complete information and standard observation regarding their administration (e.g., time, dosage, exposure, and concentration), and certain parameters (temperature, pH, and salinity) should also noted before their use in aquaculture. This review aims to critically analyze and thoroughly discuss the meta-role of various nanoparticles regarding disease control, drug delivery, water treatment, nutrition, and growth performance as well as their toxicological impacts in fish aquaculture. [ABSTRACT FROM AUTHOR]

• Ozonation enhanced the formation potential of regulated DBPs from Phe chlorination. • CH with highest yield of 21.31+1.05 ug/mgPhe was enhanced to 3 times after ozonation. • The DBPs formation rates in the first 6 h were much higher than subsequent time. • Br− promoted brominated DBPs generation and elevated the total cytotoxicity. • Ozonation enhanced the BIF of THMs, while reduced that of DHAAs. As a strong oxidizing agent, ozone is used in some water treatment facilities for disinfection, taste and odor control, and removal of organic micropollutants. Phenylalanine (Phe) was used as the target amino acid to comprehensively investigate variability of disinfection byproducts (DBPs) formation during chlorine disinfection and residual chlorine conditions subsequent to ozonation. The results showed that subsequent to ozonation, the typical regulated and unregulated DBPs formation potential (DBPsFP), including trichloromethane (TCM), dichloroacetonitrile (DCAN), chloral hydrate (CH), dichloroacetic acid (DCAA), trichloroacetic acid (TCAA), and trichloroacetamide (TCAcAm) increased substantially, by 2.4, 3.3, 5.6, 1.2, 2.5, and 6.0 times, respectively, compared with only chlorination. Ozonation also significantly increased the DBPs yield under a 2 day simulated residual chlorine condition that mimicked the water distribution system. DBPs formations followed pseudo first order kinetics. The formation rates of DBPs in the first 6 hr were higher for TCM (0.214 hr−1), DCAN (0.244 hr−1), CH (0.105 hr−1), TCAcAm (0.234 hr−1), DCAA (0.375 hr−1) and TCAA (0.190 hr−1) than thereafter. The peak DBPsFP of TCM, DCAN, CH, TCAcAm, DCAA, and TCAA were obtained when that ozonation time was set at 5–15 min. Ozonation times > 30 min increased the mineralization of Phe and decreased the formation of DBPs upon chlorination. Increasing bromine ion (Br−) concentration increased production of bromine- DBPs and decreased chlorine-DBPs formation by 59.3%–92.2%. Higher ozone dosages and slight alkaline favored to reduce DBP formation and cytotoxicity. The ozonation conditions should be optimized for all application purposes including DBPs reduction. [Display omitted] [ABSTRACT FROM AUTHOR]

The industrial laundry sector is a major user of water and chemicals such as surfactants, and one of the largest producers of wastewater. Although treated wastewaters comply with regulations, they still contain contaminants. Here we review laundry wastewater with focus on industrial laundry activities and their challenges, chemical composition of wastewater, and treatment techniques. We discuss advantages and drawbacks of treatment techniques that can be used as secondary treatment in already existing plants, or as tertiary treatment, i.e., complementary to an existing treatment. We observe that laundry is an expanding industrial sector with increasing water requirements, an abundant use of chemical substances, and increasingly stringent discharge regulations. There is a lack of chemical and biological knowledge on aqueous discharges. Moreover, the chemical composition, temporal variability, treatment information, and environmental and ecotoxicological data are poorly reported. The composition of wastewaters and additives, and their temporal variability are also poorly known. Similarly, detailed information on treatments is rare, and environmental and ecotoxicological data are poorly reported. Finding a tertiary water treatment process that is efficient, viable, and environmentally friendly is challenging since wastewater volumes are very high and contaminants are present at trace level in complex organo-mineral mixtures. [ABSTRACT FROM AUTHOR]

The evolution of the modern world necessitates the establishment of diverse industrial sectors, but it is crucial to prioritize sustainability in the process. Many of these industries discharge organic pollutants indiscriminately into aqueous environments, contributing to human and aquatic health consequences. The incorporation of advanced oxidation processes has emerged as a strategy for removing organic contaminants present in wastewater. Sonolytic degradation, a form of advanced oxidation process (AOP), effectively tackles organic pollutants in wastewater, yet it comes with inherent limitations. In addressing limitations, hybrid techniques integrating ultrasound with other AOPs enhance efficiency in wastewater pollutant removal. The combination of ultrasound in conjunction with AOPs, such as heterogeneous approaches like ultrasound combined with metal ions, metal oxides, and photocatalysis, as well as homogeneous methods like ultrasound paired with peroxymonosulfate and persulfate, effectively breaks down organic pollutants. This review emphasizes the efficacy of ultrasound-based hybrid techniques for degrading organic pollutants in aqueous solutions, highlighting their distinct advantages in water treatment. [ABSTRACT FROM AUTHOR]