Plant-substrate biochar properties critical for mediating reductive debromination of 1,2-dibromoethane.

Dibromoethane is a widespread, persistent organic pollutant. Biochars are known mediators of reductive dehalogenation by layered FeII-FeIII hydroxides (green rust), which can reduce 1,2-dibromoethane to innocuous bromide and ethylene. However, the critical characteristics that determine mediator functionality are lesser known. Fifteen biochar substrates were pyrolyzed at 600 °C and 800 °C, characterized by elemental analysis, X-ray photo spectrometry C and N surface speciation, X-ray powder diffraction, specific surface area analysis, and tested for mediation of reductive debromination of 1,2-dibromoethane by a green rust reductant under anoxic conditions. A statistical analysis was performed to determine the biochar properties, critical for debromination kinetics and total debromination extent. It was shown that selected plant based biochars can mediate debromination of 1,2-dibromoethane, that the highest first order rate constant was 0.082/hr, and the highest debromination extent was 27% in reactivity experiments with 0.1 µmol (20 µmol/L) 1,2-dibromoethane, ≈ 22 mmol/L FeIIGR, and 0.12 g/L soybean meal biochar (7 days). Contents of Ni, Zn, N, and P, and the relative contribution of quinone surface functional groups were significantly (p < 0.05) positively correlated with 1,2-dibromoethane debromination, while adsorption, specific surface area, and the relative contribution of pyridinic N oxide surface groups were significantly negatively correlated with debromination.

Interface coupling to improve O2 adsorption and accelerate charge separation for boosting photocatalytic performance of ZnO/ZnIn2S4 composite in H2O2 production and environmental remediation.

The key to heterogeneous photo-Fenton technology lies in the efficient generation of hydrogen peroxide (H2O2). Herein, a newly-designed ZnO/ZnIn2S4 composite with heterostructure is synthesized. Benefiting from the formation of built-in electric field, the recombination of photoinduced electrons and holes is suppressed and interfacial charge transfer resistance is reduced. Importantly, the embedding of ZnO in ZnIn2S4 can improve the hydrophobicity and create microscopic three-phase interface, thereby boosting the capture capability for O2 and providing the convenience for the occurrence of O2 reduction reaction. More interestingly, the existence of ZnIn2S4 in the ZnO/ZnIn2S4 composite can reduce the Gibbs free energy (ΔG) of key intermediate (OOH*) formation, which will accelerate the generation of H2O2. As a result, the ZnO/ZnIn2S4 composite displays excellent performance in photocatalytic H2O2 production, and the highest yield was about 897.6 µmol/g/h within 60 min under visible light irradiation. The transfer of photoinduced carriers follows the S-scheme type mechanism. The photogenerated holes can be captured by drug residues (i.e., diclofenac sodium) to accelerate H2O2 production, while generated H2O2 can combine with Fe2+ to construct photo-Fenton system for achieving the advanced degradation of diclofenac sodium, which was mainly related to the formation of OH•. Furthermore, generated H2O2 can be applied for performing the inactivation of pathogenic bacteria. In short, current work will provide a valuable reference for future research.

Recycled waste substrates: A systematic review.

The growing interest in utilizing recycled waste substrates (RWS) in ecosystem services and environmental remediation aligns with the "waste to wealth" concept and the Sustainable Development Goals (SDGs). Despite the promising potential of RWS, research gaps remain due to a lack of comprehensive reviews on their production and applications. This systematic review attempts to synthesize and critically assess the scientific footprint of RWS through robust methodology and thorough investigation. Characterization of scientific literature, network analysis, and systematic review were conducted on articles indexed in the Web of Science and Scopus databases. Quantitative and qualitative analyses were performed on 140 articles selected by the rigorous article screening process executed using the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) protocol. The findings map the scientific literature and research themes in RWS. Around 66 % of studies in RWS used a multiple research approach, primarily experiments with case studies. Key research topics identified include (A) Technical domains - types of wastes and recycling techniques in RWS production and parameters influencing the substrate quality; (B) Application domains: environmental remediation of soil and agriculture and horticulture. The use of RWS in urban green infrastructure, particularly for green roofs and vegetative walls, and the potential for LCA studies on RWS production and applications emerge as promising areas for future research. This systematic review also presents a conceptual framework model (CFM) on RWS research, encapsulating the state-of-the-art themes, risks, limitations and constraints, and future research avenues.

Biochar-enhanced bioremediation of eutrophic waters impacted by algal blooms.

The permanent problem of formation of algal blooms in water polluted with nitrogen and phosphorus is one of the formidable environmental problems. Biochar has the potential to solve the issues related to eutrophication due to its special structure and ability to absorb the nutrients. Biochar's exceptional nutrient absorption capacity allows it to absorb excess nutrients, causing the algae to use fewer nutrients. This review deals with effective performance of biochar in reducing the effects caused by algal blooms and improving the environmental conditions. Besides, an analysis of the issues involved addresses the origins and consequences of nitrogen and phosphorus pollution, and the formation of algal blooms is also reviewed. It then delves deeply into biochar, explaining its properties, production methods, and their uses in environmental contexts. The review emphasizes that biochar can be effective in dealing with many challenges associated with environments affected by algal blooms, specifically focusing on the positive effects of biochar and algae to examine their roles in controlling algae growth. Finally, the review emphasizes new achievements and innovative ideas to foster sustainable aquatic ecosystems. The discussions emphasize the central role of biochar in managing nutrient-rich waters and algal blooms.

Heterointerface engineering of MXene: Advanced applications in environmental remediation.

Contemporary global industrialization, coupled with the relentless growth of the population, has led to a persistent escalation in the emission and accumulation of various toxic and harmful chemicals in the environment, severely disrupting the ecological balance. The development of efficient environmental cleanup materials is a crucial scientific and technological concern. Since the groundbreaking work on Ti3C2Tx in 2011, there has been a huge growing interest in MXene-based composites developed through heterointerface engineering due to its high surface area, hydrophilicity, eco-friendliness, biocompatibility, easy functionalization, excellent thermal/mechanical properties, metal conductivity and rich electronic density. In the area of environmental remediation, MXene-based composites obtained through heterointerface engineering strategies have the ability to effectively remove and systematically monitor contaminants in comparison to virgin MXene, thanks to the synergistic effects and complementary benefits. Heterointerface engineering strategy increases specific surface area, introduces catalytic sites, constructs heterojunctions/Schottky junctions, and facilitates carrier migration and electron-hole separation. These novel MXene-based composites represent significant advances in MXene research and deserve a comprehensive review. Although several excellent reviews and perspectives on the application of MXene-based composites in environmental remediation have been published, there is still a scarcity of comprehensive and systematic assessments on the reliable data and mechanisms of various MXene-based composite materials for pollutant removal and monitoring. In this focused review, the first part briefly introduces the common preparation strategies and characterization methods of single MXene and MXene-based composites, and the second part details the innovative application of MXene-based composites (involving the amalgamation of MXene with metal oxides, metal sulfide, g-C3N4, layered double hydroxides, metal-organic frameworks, single atom/quantum dots, polymers, etc.) in the field of environmental remediation, including carbon dioxide reduction, nitrogen monoxide and volatile organic compounds removal, antibiotic and heavy metal ions degradation, summarizing the relevant performance and mechanisms. Furthermore, the recent advancements in the utilization of MXene-based composites for the sensing of emerging environmental contaminants (antibiotic and antibiotic resistance genes) are summarized. Finally, an outline of the existing challenges and future prospects on this exciting field was narrated for plausible real-world use. This review will help to inspire the diverse design of MXene-based composites and to advance research related to their application in the environmental sector.

Harnessing microbes to pioneer environmental biophotoelectrochemistry.

In seeking sustainable environmental strategies, microbial biophotoelectrochemistry (BPEC) systems represent a significant advancement. In this review, we underscore the shift from conventional bioenergy systems to sophisticated BPEC applications, emphasizing their utility in leveraging solar energy for essential biochemical conversions. Recent progress in BPEC technology has facilitated improved photoelectron transfer and system stability, resulting in substantial advancements in carbon and nitrogen fixation, degradation of pollutants, and energy recovery from wastewater. Advances in system design and synthetic biology have expanded the potential of BPEC for environmental clean-up and sustainable energy generation. We also highlight the challenges of environmental BPEC systems, ranging from performance improvement to future applications.

Enhancing soil health, microbial count, and hydrophilic methomyl and hydrophobic lambda-cyhalothrin remediation with biochar and nano-biochar.

Pesticide contamination and soil degradation present significant challenges in agricultural ecosystems, driving extensive exploration of biochar (BC) and nano-biochar (NBC) as potential solutions. This study examines their effects on soil properties, microbial communities, and the fate of two key pesticides: the hydrophilic methomyl (MET) and the hydrophobic lambda-cyhalothrin (LCT), at different concentrations (1%, 3%, and 5% w w-1) in agricultural soil. Through a carefully designed seven-week black bean pot experiment, the results indicated that the addition of BC/NBC significantly influenced soil dynamics. Soil pH and moisture content (MC) notably increased, accompanied by a general rise in soil organic carbon (SOC) content. However, in BC5/NBC5 treatments, SOC declined after the 2nd or 3rd week. Microbial populations, including total plate count (TPC), phosphate-solubilizing bacteria (PSB), and nitrogen-fixing bacteria (NFB), showed dynamic responses to BC/NBC applications. BC1/NBC1 and BC3/NBC3 applications led to a significant increase in microbial populations, whereas BC5/NBC5 treatments experienced a decline after the initial surge. Furthermore, the removal efficiency of both MET and LCT increased with higher BC/NBC concentrations, with NBC demonstrating greater efficacy than BC. Degradation kinetics, modeled by a first-order equation, revealed that MET degraded faster than LCT. These findings underscore the profound impact of BC/NBC on pesticide dynamics and microbial communities, highlighting their potential to transform sustainable agricultural practices.

Potential for high-grade recovery of rare earth elements and cobalt from acid mine drainage via adsorption to precipitated manganese (IV) oxides.

High demand for rare earth elements (REEs) has increased interest in their recovery from unconventional sources, such as acid mine drainage (AMD). AMD contains elevated concentrations of Mn, Fe, and Al, which precipitate as (oxy)hydroxide minerals as pH is raised. These precipitates can remove cations including REEs and Co from solution via sorption and/or coprecipitation. In this study we developed a method to recover these critical minerals by sorption to MnO2, precipitated by oxidation of in situ Mn (II) with added KMnO4 at acidic pH. MnO2 solids were prepared with varying concentrations of KMnO4, SO42-, and Cl-, to elucidate the effects of excess KMnO4, SO42- concentration, and ionic strength on adsorption. When using a stoichiometric ratio of Mn (II) and KMnO4, 100% removal of REEs and Co occurred at approximately pH 3.5, nearly 2 pH units lower than was observed by sorption to Fe and Al hydroxysulfates. When using excess KMnO4 nearly 100% removal of REEs and Co was accomplished at approximately pH 2, although SO42- was found to inhibit REE sorption. From these results, we developed a two-stage process for recovery of REEs from AMD; a preliminary pH adjustment to remove Fe and Al hydroxy-sulfates, followed by adding KMnO4, precipitating MnO2, enabling recovery of REEs and Co. We tested this process in a representative synthetic AMD, achieving a grade of 6.16 mg REEs per g of solid, which is 65 % of the maximum possible grade based on solution composition. Fractionation of REEs was observed, with light REEs (LREEs) preferentially sorbed to MnO2 relative to both medium REEs (MREEs) and heavy REEs (HREEs). In contrast, preferential sorption of HREEs was observed for sorption to Fe and Al oxyhydroxides at all pH ranges. These results suggest the mechanisms of REE sorption differ among the solids and warrant further study.

3D-Printed MOF Monoliths: Fabrication Strategies and Environmental Applications.

Metal-organic frameworks (MOFs) have been extensively considered as one of the most promising types of porous and crystalline organic-inorganic materials, thanks to their large specific surface area, high porosity, tailorable structures and compositions, diverse functionalities, and well-controlled pore/size distribution. However, most developed MOFs are in powder forms, which still have some technical challenges, including abrasion, dustiness, low packing densities, clogging, mass/heat transfer limitation, environmental pollution, and mechanical instability during the packing process, that restrict their applicability in industrial applications. Therefore, in recent years, attention has focused on techniques to convert MOF powders into macroscopic materials like beads, membranes, monoliths, gel/sponges, and nanofibers to overcome these challenges.Three-dimensional (3D) printing technology has achieved much interest because it can produce many high-resolution macroscopic frameworks with complex shapes and geometries from digital models. Therefore, this review summarizes the combination of different 3D printing strategies with MOFs and MOF-based materials for fabricating 3D-printed MOF monoliths and their environmental applications, emphasizing water treatment and gas adsorption/separation applications. Herein, the various strategies for the fabrication of 3D-printed MOF monoliths, such as direct ink writing, seed-assisted in-situ growth, coordination replication from solid precursors, matrix incorporation, selective laser sintering, and digital light processing, are described with the relevant examples. Finally, future directions and challenges of 3D-printed MOF monoliths are also presented to better plan future trajectories in the shaping of MOF materials with improved control over the structure, composition, and textural properties of 3D-printed MOF monoliths.

Overlooked Roles and Transformation of Carbon-Centered Radicals Produced from Natural Organic Matter in a Thermally Activated Persulfate System.

The presence and induced secondary reactions of natural organic matter (NOM) significantly affect the remediation efficacy of in situ chemical oxidation (ISCO) systems. However, it remains unclear how this process relates to organic radicals generated from reactions between the NOM and oxidants. The study, for the first time, reported the vital roles and transformation pathways of carbon-centered radicals (CCR•) derived from NOM in activated persulfate (PS) systems. Results showed that both typical terrestrial/aquatic NOM isolates and collected NOM samples produced CCR• by scavenging activated PS and greatly enhanced the dehalogenation performance under anoxic conditions. Under oxic conditions, newly formed CCR• could be oxidized by O2 and generate organic peroxide intermediates (ROO•) to catalytically yield additional •OH without the involvement of PS. Nuclear magnetic resonance (NMR) and Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR-MS) results indicated that CCR• predominantly formed from carboxyl and aliphatic structures instead of aromatics within NOM through hydrogen abstraction and decarboxylation reactions by SO4•- or •OH. Specific anoxic reactions (i.e., dehalogenation and intramolecular cross-coupling reactions) further promoted the transformation of CCR• to more unsaturated and polymerized/condensed compounds. In contrast, oxic propagation of ROO• enhanced bond breakage/ring cleavage and degradation of CCR• due to the presence of additional •OH and self-decomposition. This study provides novel insights into the role of NOM and O2 in ISCO and the development of engineered strategies for creating organic radicals capable of enhancing the remediation of specific contaminants and recovering organic carbon.

Advanced Characterization Techniques and Theoretical Calculation for Single Atom Catalysts in Fenton-like Chemistry.

Single-atom catalysts (SACs) have attracted extensive attention due to their unique catalytic properties and wide range of applications. Advanced characterization techniques, such as energy-dispersive X-ray spectroscopy, X-ray photoelectron spectroscopy, transmission electron microscopy, scanning electron microscopy, and X-ray absorption fine-structure spectroscopy, have been used to investigate the elemental compositions, structural morphologies, and chemical bonding states of SACs in detail, aiming at unraveling the catalytic mechanism. Meanwhile, theoretical calculations, such as quantum chemical calculations and kinetic simulations, were used to predict the catalytic reaction pathways, active sites, and reaction kinetic behaviors of SACs, providing theoretical guidance for the design and optimization of SACs. This review overviews advanced characterization techniques and theoretical calculations for SACs in Fenton-like chemistry. Moreover, this work highlights the importance of advanced characterization techniques and theoretical calculations in the study of SACs and provides perspectives on the potential applications of SACs in the field of environmental remediation and the challenges of practical engineering.

Functional Bio-Based Polymeric Hydrogels for Wastewater Treatment: From Remediation to Sensing Applications.

In recent years, many researchers have focused on designing hydrogels with specific functional groups that exhibit high affinity for various contaminants, such as heavy metals, organic pollutants, pathogens, or nutrients, or environmental parameters. Novel approaches, including cross-linking strategies and the use of nanomaterials, have been employed to enhance the structural integrity and performance of the desired hydrogels. The evolution of these hydrogels is further highlighted, with an emphasis on fine-tuning features, including water absorption capacity, environmental pollutant/factor sensing and selectivity, and recyclability. Furthermore, this review investigates the emerging topic of stimuli-responsive smart hydrogels, underscoring their potential in both sorption and detection of water pollutants. By critically assessing a wide range of studies, this review not only synthesizes existing knowledge, but also identifies advantages and limitations, and describes future research directions in the field of chemically engineered hydrogels for water purification and monitoring with a low environmental impact as an important resource for chemists and multidisciplinary researchers, leading to improvements in sustainable water management technology.

Facile synthesis and optimization of Acacia senegal gum hydrogel for kinetically treated adsorptive removal of targeted industrial effluents.

This context summarizes a detail on the fabrication of Acacia senegal Gum Hydrogel (ASGh) within well-engineered microemulsion, and thereafter chemical modification for environmental remediation. In brief, Divinylsulfone was used to crosslink polymeric chains and produce ASGh in ˂50 µm size within the reverse-microemulsion of Natrium-bis-(2-ethylhexyl) sulfosuccinate in gasoline. ASGh were subjected to chemical modification via versatile diethylenetriamine to produce m-[ASGh] for adsorptive removal of methyl orange (MO), eosin Y (EY) and congo red (CR) from waste-water. ASGh and m-[ASGh] were characterized through Scanning Electron Microscopy (SEM), Fourier Transform Infrared Spectroscopy (FTIR), and zeta potential measurements. For instance, FT-IR spectra depicted new bands upon Diethylenetriamine modification. The zeta potential measurements confirm a positively charged surface of m-[ASGh] upon Diethylenetriamine addition. Interestingly, 0.05 g m-[ASGh] demonstrated 91.0, 84.1, and 73.0 % removal efficiency towards MO, EY and CR, respectively in 2 h equilibrium time. Langmuir, Freundlich and modified-Freundlich isotherms were applied to further delineate adsorption data. Modified-Freundlich model depicted comparatively more agreeable fit, and delivered R2 value nearer to unity. Further, 143 mg·g-1, 130 mg·g-1 and, 116 mg·g-1 maximum adsorption capacity (QM) was represented by m-[ASGh] towards MO, EY and CR, respectively in 2 h. Interestingly, real water sample were tested whereby, the QM against MO, EY and CR was 146 mg·g-1, 132 mg·g-1 and, 111 mg·g-1, respectively in 2 h equilibrium time. To conclude, m-[ASGh] could be treated as decolorizing agent in real waste-water polluted through negatively charged organic pollutants, particularly MO.

Efficient nitrite determination by electrochemical approach in liquid phase with ultrasonically prepared gold-nanoparticle-conjugated conducting polymer nanocomposites.

An electrochemical nitrite sensor probe is introduced herein using a modified flat glassy carbon electrode (GCE) and SrTiO3 material doped with spherical-shaped gold nanoparticles (Au-NPs) and polypyrrole carbon (PPyC) at a pH of 7.0 in a phosphate buffer solution. The nanocomposites (NCs) containing Au-NPs, PPyC, and SrTiO3 were synthesized by ultrasonication, and their properties were thoroughly characterized through structural, elemental, optical, and morphological analyses with various conventional spectroscopic methods, such as field-emission scanning electron microscopy, energy-dispersive X-ray spectroscopy, high-resolution transmission electron microscopy, powder X-ray diffraction, X-ray photoelectron spectroscopy, and Brunauer-Emmett-Teller method. The peak currents due to nitrite oxidation were characterized in detail and analyzed using conventional cyclic voltammetry (CV) as well as differential pulse voltammetry (DPV) under ambient conditions. The sensor response increased significantly from 0.15 to 1.5 mM of nitrite ions, and the sensor was fabricated by coating a conducting agent (PEDOT:PSS) on the GCE to obtain the Au-NPs/PPyC/SrTiO3 NCs/PEDOT:PSS/GCE probe. The sensor's sensitivity was determined as 0.5 µA/µM∙cm2 from the ratio of the slope of the linear detection range by considering the active surface area (0.0316 cm2) of the flat GCE. In addition, the limit of detection was determined as 20.00 ± 1.00 µM, which was found to be satisfactory. The sensor's stability, pH optimization, and reliability were also evaluated in these analyses. Overall, the sensor results were found to be satisfactory. Real environmental samples were then analyzed to evaluate the sensor's reliability through DPV, and the results showed that the proposed novel electrochemical sensor holds great promise for mitigating water contamination in the real samples with the lab-made Au-NPs/PPyC/SrTiO3 NC. Thus, this study provides valuable insights for improving sensors for broad environmental monitoring applications using the electrochemical approach.

Hematite nanomaterial from a tropical freshwater ecosystem: Geological, environmental, and industrial implications.

Synthetic hematite (Fe2O3) nanoparticles are extensively explored for medicine, optics, and environmental remediation. However, natural iron nanoparticles in a freshwater ecosystem have not been well characterized. Here we report the presence of natural iron nanoparticles in a tropical freshwater ecosystem in southern India. These iron nanoparticles that exist as slime in the natural water system were characterized through a multiproxy investigation involving Field-Emission Scanning Electron Microscopy (FE-SEM), X-ray Diffraction (XRD), X-ray Fluorescence (XRF), X-ray Photoelectron Spectroscopy (XPS), and Raman spectroscopy and BET analyses. These nanoparticles exist as amorphous hematite (Fe2O3), with the XRD peaks matching that of the iron arsenate compound. Fe2O3 occurs as mesoporous hollow microspheres with a size range of 14.97 to 61.3 nm and a surface area of 48.45m2/g. Further, the identification of Bacillus cereus in the slime suggests its role in iron sequestration, indicating a biogeochemical origin, which we infer is a particularly common phenomenon in tropical river basins where lateritic soils prevail. This study is the first to describe natural iron nanoparticles in a tropical freshwater ecosystem. It identifies their amorphous hematite structure and biogeochemical origin, offering new insights into their ecological roles and potential applications. This discovery presents an opportunity for utilizing this slime as an important source of hematite nanomaterials, with potential industrial applications.

Chitosan-blended membranes for heavy metal removal from aqueous systems: A review of synthesis, separation mechanism, and performance.

The environmental pollution caused by heavy metal ions has become a serious global environmental issue. Heavy metal contaminants released from industrial effluents, agricultural runoff, and human activities, can enter into water resources. The toxicity of these heavy metal ions even at trace concentrations presents a substantial hazard to both aquatic systems and human well-being. The membrane separation processes have become more promising sustainable techniques for the separation of metal ions from the effluent. The research efforts have been concentrated on improving the synthesis of membranes and membrane materials to facilitate the sustainable separation of heavy metals. The application of chitosan in the fabrication of membranes is getting more attention. Chitosan, a natural polysaccharide derived from chitin, is abundant in nature and has active hydroxyl and amino groups suitable for the separation of heavy metal ions. It exhibits excellent chelating tendency, biocompatibility, and biodegradability. The functionalization of chitosan to improve its mechanical strength, chemical stability, and antifouling properties has become an ongoing area of research. This review examines the synthesis and efficient applications of chitosan blended membranes. The review concludes by outlining the current challenges and proposing future research prospects to enhance the applicability of chitosan-blended membranes in environmental remediation.

Bibliometric analysis of research trends in biogranulation technology for wastewater treatment.

Inadequate management and treatment of wastewater pose significant threats, including environmental pollution, degradation of water quality, depletion of global water resources, and detrimental effects on human well-being. Biogranulation technology has gained increasing traction for treating both domestic and industrial wastewater, garnering interest from researchers and industrial stakeholders alike. However, the literature lacks comprehensive bibliometric analyses that examine and illuminate research hotspots and trends in this field. This study aims to elucidate the global research trajectory of scientific output in biogranulation technology from 1992 to 2022. Utilizing data from the Scopus database, we conducted an extensive analysis, employing VOSviewer and the R-studio package to visualize and map connections and collaborations among authors, countries, and keywords. Our analysis revealed a total of 1703 journal articles published in English. Notably, China emerged as the leading country, Jin Rencun as the foremost author, Bioresource Technology as the dominant journal, and Environmental Science as the prominent subject area, with the Harbin Institute of Technology leading in institutional contributions. The most prominent author keyword identified through VOSviewer analysis was "aerobic granular sludge," with "sequencing batch reactor" emerging as the dominant research term. Furthermore, our examination using R Studio highlighted "wastewater treatment" and "sewage" as notable research terms within the field. These findings underscore a diverse research landscape encompassing fundamental aspects of granule formation, reactor design, and practical applications. This study offers valuable insights into biogranulation potential for efficient wastewater treatment and environmental remediation, contributing to a sustainable and cleaner future.

A microbiome-biochar composite synergistically eliminates the environmental risks of antibiotic mixtures and their toxic byproducts.

This study developed a continuous reactor system employing a hybrid hydrogel composite synthesized using a complex sludge microbiome and an adsorbent (HSA). This HSA-based system effectively eliminated the environmental risks associated with a mixture of the antibiotics ciprofloxacin and sulfamethoxazole, which exhibited higher toxicity in combination than individually at environmentally relevant levels. Analytical chemistry experiments revealed the in-situ generation of various byproducts (BPs) within the bioreactor system, with two of these BPs recording toxicity levels that surpassed those of their parent compound. The HSA approach successfully prevented the functional microbiome from being washed out of the reactor, while HSA efficiently removed antibiotic residues in their original and BP forms through synergistic adsorptive and biotransformation mechanisms, ultimately reducing the overall ecotoxicity. The use of HSA thus demonstrates promise not only as a mean to reduce the threat posed by toxic antibiotic residues to aquatic ecosystems but also as a practical solution to operational challenges, such as biomass loss/washout, that are frequently encountered in various environmental bioprocesses.

Defect and Heterostructure engineering assisted S-scheme Nb2O5 nanosystems-based solutions for environmental pollution and energy conversion.

This review explores the crystallographic versatility of niobium pentoxide (Nb2O5) at the nanoscale, showcasing enhanced catalytic efficiency for cutting-edge sustainable energy and environmental applications. The synthesis strategies explored encompass defect engineering, doping engineering, s-scheme formation, and heterojunction engineering to fine-tune the physicochemical attributes of diverse dimensional (0-D, 1-D, 2-D, and 3-D) Nb2O5 nanosystems as per targeted application. In addressing escalating environmental challenges, Nb2O5 emerges as a semiconductor photocatalyst with transformative potential, spanning applications from dye degradation to antibiotic and metal removal. Beyond its environmental impact, Nb2O5 is pivotal in sustainable energy applications, specifically in carbon dioxide and hydrogen conversion. However, challenges such as limited light absorption efficiency and scalability in production methods prompt the need for targeted research endeavors. The review details the state-of-the-art Nb2O5 nanosystems engineering, tuning their physicochemical properties employing material engineering, and their high catalytic performance in environment remediation and energy generation. It outlines challenges, potential mitigation strategies, and prospects, urging for developing greener synthesis routes, advanced charge transfer techniques, targeted optimization for specific pollutants, and application for micro/nano plastics photocatalytic reduction. As researchers and environmental stewards collaborate, Nb2O5 stands poised at the intersection of environmental remediation, energy harvesting, and nanomaterial advancements, offering a beacon of progress toward a cleaner, more sustainable future.

Enhanced efficiency and stability in the degradation of triazophosphorus pesticides by Al6Si2O13/WO2.72 nanocomposites through synergistic action of S-scheme heterojunction and oxygen vacancies.

The environmental contamination caused by organophosphorus pesticides (for example, triazophos) is an escalating concern. To mitigate this issue, this study introduces a novel Al6Si2O13/WO2.72 (ASO/WO) nanocomposite photocatalyst, which markedly enhances the photocatalytic degradation of triazophos. The optimized nanocomposite material with a 60.0 % ASO loading (60-ASO/WO) achieves a degradation rate of 86.3 % for triazophos within 140.0 min, marginally exceeding 60-ASO/WO3 (72.6 %) and significantly outperforming individual ASO (65.0 %), WO (59.5 %), and WO3 (56.2 %). This catalyst retains 88.9 % of its activity after five cycles, showcasing exceptional efficiency and stability. Additionally, its electrochemical surface area (ECSA, 310.0 cm2), total organic carbon (TOC, removal rate of 73.7 %), photocurrent, and electrochemical impedance are all optimal. X-ray photoelectron spectroscopy (XPS), electron paramagnetic resonance (EPR), and theoretical calculations elucidate the critical role of oxygen vacancies and the S-scheme heterojunction in augmenting charge separation and photocatalytic performance, corroborating the synergistic effect of oxygen defects and the S-scheme. While individual factors can enhance photocatalytic activity, their combination results in a more pronounced effect. Liquid chromatography-mass spectrometry (LCMS) identifies the principal degradation intermediates, including 1-phenyl-3-hydroxy-1, 2, 4-triazole, diethyl thiophosphate, and 3, 5, 6-trichloro-2-pyridinol, underscoring the material's potential in environmental remediation.