Search Results (6,549)

Currently, the potential environmental concerns around the world for polycyclic aromatic hydrocarbon carcinogenic (PAHCs) contamination as carcinogenic compounds in industrial soils (automobile industry) are rising day by day. At present, the technology of treating contaminated soils using photocatalysts is commonly used; however, this study tested photolysis and photocatalysis through ultraviolet light (306 nm) due to its high treatment efficiency. FeCl₃ (0.3, 0.4 M) was used as an iron catalyst for each treatment in the presence of H₂O₂ (10%, 20%) as an oxidizing agent. The impact of light treatment on soils that contained various concentrations of PAHCs like naphthalene (NAP), chrysene (CRY), benzo(a) pyrene (BaP), indeno (1,2,3-cd) pyrene (IND) was investigated. The QuEChERS method was used to extract PAHCs, and a gas chromatograph mass spectrometer (GCMSMS) was used to determine concentration. The concentrations of PAHCs were measured for soils at intervals of every 2 h after exposure to ultraviolet rays. The results showed a decrease in PAHCs concentrations with increased exposure to UV irradiation, as the initial values were 26.8 ng/g (NAP), 97 ng/g (CRY), 9.1 ng/g (BaP) and 9.7 ng/g (IND), which decreased to 2.17 ng/g (NAP), 3.14 ng/g (CRY), 0.33 ng/g (BaP) and 0.46 ng/g (IND) at 20, 40, 30 and 40 h of UV exposure; moreover, with an increase in concentration of the catalyst (0.4 M FeCl₃ with 20% H₂O₂), NAP, CRY, BaP and IND became undetectable at 8, 26, 14 and 20 h, respectively. It was concluded that a significant effect of ultraviolet rays on the photolysis of PAHCs, along with Photovoltaic at 306 nm wavelength, was observed while using FeCl₃ (0.4 M) combined with H₂O₂ (20%) produced better results in a shorter time compared to FeCl₃ (0.3 M) with H₂O₂ (10%). Full article

Lead (Pb) in soil poses serious environmental and health risks, and its removal requires complex and costly treatment methods to meet strict regulatory standards. To effectively address this challenge, innovative and efficient techniques are essential. Sepiolite-supported MnFe₂O₄ (MnFe₂O₄/SEP) composites were synthesized via a chemical co-precipitation method. The effects of MnFe₂O₄/SEP on soil pH, cation exchange capacity (CEC), available Pb content, Pb²⁺ uptake, and the activities of antioxidant enzymes in Brassica chinensis (Pak Choi) were examined. MnFe₂O₄/SEP showed superior Pb²⁺ adsorption compared to SEP alone, fitting Langmuir models, Dubinin-Radushkevich (D-R) models, Temkin models and pseudo-second-order kinetics. The maximum adsorption capacities at 298, 308, and 318 K were 459, 500 and 549 mg·g⁻¹, respectively. XPS analysis indicated that chemisorption achieved through ion exchange between Pb²⁺ and H⁺ was the main mechanism. MnFe₂O₄/SEP increased the soil pH by 0.2–1.5 units and CEC by 18–47%, while reducing available Pb by 12–83%. After treatment with MnFe₂O₄/SEP, acid-extractable and reducible Pb in the soil decreased by 14% and 39%, while oxidizable and residual Pb increased by 26% and 21%, respectively. In Brassica chinensis, MnFe₂O₄/SEP reduced Pb²⁺ uptake by 76%, increased chlorophyll content by 36%, and decreased malondialdehyde (MDA) levels by 36%. The activities of antioxidant enzymes—superoxide dismutase (SOD), peroxidase (POD), and catalase (CAT)—were decreased by 29%, 38% and 17%, respectively. These findings demonstrate that MnFe₂O₄/SEP is an efficient Pb²⁺ adsorbent that immobilizes Pb in soil mainly through ion exchange, thereby providing a highly effective strategy for remediating Pb-contaminated soils and improving plant health. Full article

Microplastics (MPs), as an emerging persistent contaminant, pose a potential threat to ecosystems and human health. The adsorptive removal of MPs from aqueous environments using magnetic nanoparticles has become a particularly promising remediation technology. Nevertheless, there remain significant knowledge gaps regarding its adsorption mechanism, especially how the key physical properties of magnetic nanoparticles regulate their adsorption behavior towards MPs. This study first investigated the relationship between the particle size of Fe₃O₄ nanoparticles and their adsorption efficacy for MPs. The results demonstrated a non-monotonic, size-dependent adsorption of MPs by Fe₃O₄ nanoparticles, with the adsorption efficiency and capacity following the order: 300 nm > 15 nm > 100 nm. This non-linear relationship suggested that factors other than specific surface area (which would favor smaller particles) are significantly influencing the adsorption process. Isotherm analysis indicated that the adsorption is not an ideal monolayer coverage process. Kinetic studies showed that the adsorption process could be better described by the pseudo-second-order model, while intra-particle diffusion played a critical role throughout the adsorption process. Furthermore, the effect of pH on adsorption efficiency was examined, revealing that the optimal performance occurs under neutral to weak acidic conditions, which is consistent with measurements of surface charges of nanoparticles. These findings suggest that the adsorption is not determined by specific surface area but is dominated by electrostatic interactions. The size-dependent adsorption of MPs by Fe₃O₄ nanoparticles provides new insights for the modification of magnetic adsorbents and offers a novel perspective for the sustainable and efficient remediation of environmental MPs pollution. Full article

Achieving selective, direct conversion of methane into value-added chemicals requires catalysts that can navigate the intrinsic trade-off between C–H bond activation and over-dehydrogenation. Transition metal phosphides (TMPs) have emerged as promising catalysts that can tune this selectivity. This work utilizes density functional theory (DFT) to systematically assess how the transition metal’s identity (M = Fe, Co, Ni) in isostructural M₂P phosphides governs this balance. The findings reveal that the high reactivity of Fe₂P and Co₂P, which facilitates initial methane activation, also promotes facile deep dehydrogenation pathways to coke precursors like CH*. In stark contrast, Ni₂P exhibits a moderated reactivity that kinetically hinders CH* formation while simultaneously exhibiting the lowest activation barrier for the C–C coupling of CH₂* intermediates to form ethylene. This revealed trade-off between the high reactivity of Fe/Co phosphides and the high selectivity of Ni₂P offers a guiding principle for the rational design of advanced bimetallic phosphides for efficient methane upgrading. Full article

Mineral water content strongly depends on the geologic layer characteristics. Therefore, the aim of the present study is to make a comparison between two renowned mineral water sources in Romania, Borsec and Tusnad. Two public springs were selected from each location: Boldizsar (about 6600 L/day) and Lazar (about 500 L/day) from Borsec and Mikes (about 5000 L/day) and Young’s spring (about 600 L/day) from Tusnad. All investigated springs are naturally carbonated. Water properties were measured in situ and in laboratory for the collected samples; the results found that Borsec mineral water has a pH of about 7.5, while Tusnad mineral water is slightly acid (pH = 6.5). TDS strongly depends on the spring’s flow (for instance, Boldizsar has a TDS of about 900 mg/L, while Lazar has a TDS of about 1529 mg/L due to its high mineralization, while Young’s spring has a TDS of 165 mg/L due to its low mineralization, although it has low flow). Borsec mineral water has a lower salinity of about 1.22 PSU, while Tusnad water has a salinity of about 2 PSU, caused by a high amount of Na and Fe ions. Mineral waters dissolve ions from the geological layers, which react with carbonic acid during drying, generating specific crystallized compounds. The crystallized matter was investigated using XRD coupled with mineralogical optical microscopy (MOM); their microstructural features were observed using SEM coupled with elemental spectroscopy. Borsec water generates mainly Ca, Mg, and Na minerals like calcite, aragonite, pseudo-dolomite, natron, and traces of halite. Tusnad mineral waters have significant amounts of Ca, but also have Fe and much more Cl, since calcite and aragonite are mixed up with large amounts of halite and iron compounds. It looks like the presence of iron ions in the Tusnad mineral water collected from Mikes and Young’s spring explains the acidic pH. All these aspects are useful for further investigation regarding specific therapeutic purposes like chronic colitis and biliary lithiasis symptom amelioration (Boldizsar), chronic colitis, and enterocolitis symptoms (Lazar). Tusnad waters, like the water from Mikes spring, are recommended for anemia and neurasthenia, while Young’s spring is recommended for renal lithiasis amelioration. Full article

Due to its efficiency, advanced oxidation processes (AOP), such as photo-Fenton, have become an alternative for removing emerging contaminants like paracetamol. The objective of this work was to perform a life cycle assessment (LCA) according to ISO 14040/44 for a heterogeneous photo-Fenton process catalyzed by Cu/Fe-pillared clays (PILC) for the removal of paracetamol from water. The study covered catalyst synthesis and four treatment scenarios, with inventories built from experimental data and ecoinvent datasets; treatment time was 120 min per functional unit. Environmental impacts for catalyst synthesis were quantified with ReCiPe 2016 (midpoint), while toxicity-related impacts of the degradation stage were assessed with USEtox™ (human carcinogenic toxicity, human non-carcinogenic toxicity, and freshwater ecotoxicity). Catalyst synthesis dominated most midpoint categories, the global warming potential for 1 g of Cu/Fe-PILC was 10.98 kg CO₂ eq. Toxicity results for S4 (photo-Fenton Cu/Fe PILC) showed very low values: 9.73 × 10⁻¹² CTUh for human carcinogenic and 1.29 × 10⁻¹³ CTUh for human non-carcinogenic. Freshwater ecotoxicity ranged from 5.70 × 10⁻⁴ PAF·m³·day at pH 2.7 (≥60 min) to 1.67 × 10⁻⁴ PAF·m³·day at pH 5.8 (120 min). Overall, optimizing pH and reaction time, are key levers to improve the environmental profile of AOP employing Cu/Fe-PILC catalysts. Full article

Tetracycline antibiotics are widely used, but their resistance to degradation and persistence in the environment pose a potential risk of inducing antibiotic resistance, creating significant threats to both the environment and human health. This study established a laccase–mediator system (LMS) using natural green tea polyphenols (GTPs) as mediators for efficient tetracycline degradation. Through analyzing the main GTP components and optimizing the reaction conditions, the degradation efficiency of the system was evaluated. The experimental results indicated that, among the various tea polyphenol components, epicatechin gallate (ECG) contributed the most significantly to the degradation efficiency. Under optimized conditions, the Lac-ECG system degraded over 98% of tetracycline within 3–4 min. Further optimization of the Lac-GTP system allowed us to identify the following optimal conditions: a GTP concentration of 1.0 mmol/L, laccase concentration of 1.0 mg/mL, pH of 6.0, and temperature of 25 °C. Under these conditions, a degradation rate of 95.07% was attained within 5 min, outperforming a system using the synthetic mediator ABTS. Additionally, metal ions such as Ca²⁺, Mg²⁺, Cu²⁺, Fe³⁺, Fe²⁺, and Ni²⁺ were found to enhance the degradation process, while Mn²⁺ and Hg²⁺ exhibited inhibitory effects. Antibacterial activity tests revealed that the degradation products completely lost their antimicrobial activity, demonstrating effective detoxification of tetracycline. In conclusion, the tea polyphenol-based laccase–mediator system developed in this study exhibits high efficiency, cost-effectiveness, and environmental friendliness, offering a promising strategy for the remediation of tetracycline-contaminated environments. Full article

The karst landscape of Trenggalek Regency, located in several sub-districts including Dongko, Kampak, and Watulimo, is shaped by the Wonosari Formation and is characterized by springs and underground rivers. Due to water scarcity in the region, local communities heavily depend on these natural water sources. This study assesses the groundwater quality of 16 springs and 20 underground rivers to evaluate their suitability for consumption and associated health risks. Using the groundwater quality index (GWQI), human health risk assessment (HHRA), and statistical methods, various physicochemical parameters were analyzed, including pH, total dissolved solids (TDS), electrical conductivity (EC), and concentrations of iron (Fe²⁺), manganese (Mn²⁺), calcium carbonate (CaCO₃), and sulfate (SO₄). Water generally meets the World Health Organization standards for safe drinking. However, correlation analysis reveals notable mineral dissolution and possible anthropogenic influence. TDS strongly correlates with EC (r = 0.97), while Fe²⁺ shows significant relationships with Mn and TDS. Conversely, CaCO₃ shows a negative correlation with EC and TDS, suggesting alternative sources beyond rock weathering. The HHRA indicates higher non-carcinogenic health risks from Fe²⁺ contamination in underground rivers compared to springs. The study’s novelty comes in its integrated assessment of groundwater quality and health hazards in Trenggalek’s karst region, which uses GWQI, HHRA, and statistical analysis to show geochemical interactions and highlight iron-related health issues in underground rivers. Full article

The results from previous environmental studies on the physicochemical properties of bottom sediments from the Odra River estuary (SW Baltic Sea) and their contamination by pharmaceutically active compounds (PhACs) were compiled and analyzed by the use of various statistical methods (Principal Component Analysis, ANOVA/Kruskal–Wallis, Spearman correlation analysis, Partial Least Squares Discriminant Analysis, and Cluster Analysis). These studies included data on 130 PhACs determined in sediment samples collected from 70 sites across the Odra River estuary as well as the site distance to wastewater treatment plant discharge, PhACs’ physicochemical properties (Kd, Kow, pKa, solubility, metabolism), and sales data. Additionally, total organic carbon, total nitrogen, total phosphorus, acid volatile sulfides, clay mineral content, and trace elements such as As, Ba, Cd, Co, Cr, Cu, Fe, Hg, Mn, Mo, Ni, Pb, Sn, and Zn were analyzed. Clay mineral content and TP were identified as the key physicochemical factors influencing the spatial distribution of PhACs in bottom sediments, exerting a greater impact than the distance of sampling sites from WWTP discharge points. The distribution of PhACs in the estuary was also influenced by the Kd and solubility of the compounds. More soluble pharmaceuticals with low adsorption affinity to sediments were detected more frequently and transported to distant locations, whereas less soluble compounds with high adsorption affinity settled down in bottom sediments near contamination sources. Neither the proportion of a drug excreted unchanged, nor its prescription frequency and sales volume, influenced the spatial distribution of PhACs. In general, Kd may be a useful parameter in the planning of environmental monitoring and tracing migration of PhACs in aquatic environments. Full article

Plasma has become an up-and-coming advanced oxidation technology for wastewater treatment. However, its efficiency is often limited due to the lack of high-performance catalytic materials. In this study, one-dimensional carbon nanofiber precursors were first fabricated via electrospinning, followed by the in situ growth of the Zn/Fe-MOF on their surfaces. After pyrolysis at different temperatures, a series of carbon-based catalysts (FeNFC) were obtained. This new type of catalyst possesses advantages such as high porosity, a large specific surface area, and mechanical stability. Using tetracycline (TTCH) as the target pollutant, the performance of the catalyst was evaluated in the dielectric barrier discharge (DBD) system. The study showed that the addition of FeNFC significantly increased the degradation rate of TTCH in the system. Comparing different pyrolysis temperatures, at 900 °C, the comprehensive performance of the catalyst (FeNFC-900) was the best (the kinetic constant was k_obs = 0.126 min⁻¹, and the removal rate of TTCH was 91.8% within 30 min). The catalytic performance was influenced by factors such as the dosage of the catalyst, the concentration of TTCH, the power of DBD, and the initial pH. The catalytic effect of the material increased within a certain range with the increase in the catalyst dosage. The increase in TTCH concentration led to a decrease in the catalytic performance. The higher the power of the DBD, the higher the removal rate of TTCH. Moreover, when the initial pH was strongly alkaline, the catalytic effect of the catalyst was the best (k_obs = 0.275 min⁻¹, and the removal rate of TTCH was 98.7% within 30 min). Ionic interference tests demonstrated the strong resistance of FeNFC to common water matrix components, while radical quenching experiments revealed that multiple reactive species contributed to TTCH degradation. This work has broad application prospects for enhancing the efficiency of DBD systems in the removal of TTCH. Full article

This study presents the preparation of iron and nitrogen co-doped sludge-based biochar (FeCN-MSBC) and iron oxide-doped biochar (FeO-MSBC) by ball milling municipal sludge with different iron precursors (K₃Fe(CN)₆ and Fe₂O₃), followed by pyrolysis. These biochars were utilized to activate persulfate (PMS) for the degradation of phenolic pollutants. The results demonstrate that FeCN-MSBC, formed by the introduction of K₃Fe(CN)₆, contains Fe/N phases, with surface Fe sites exhibiting a lower oxidation state, which significantly enhances PMS activation efficiency. In contrast, FeO-MSBC, due to the aggregation of Fe₂O₃/Fe₃O₄, shows relatively lower catalytic activity. The FeCN-MSBC/PMS system degrades pollutants via a synergistic mechanism involving non-radical pathways mediated by ¹O₂ and electron transfer processes (ETP) catalyzed by surface Fe. Electrochemical oxidation and quenching experiments confirm that ETP is the dominant pathway. FeCN-MSBC, prepared at a pyrolysis temperature of 600 °C and an Fe loading of 3 mmol/g TSS, exhibited the best performance, achieving a phenol degradation rate constant (k_obs) of 0.127 min⁻¹, 4.5 times higher than that of undoped biochar (MSBC). FeCN-MSBC/PMS maintained high efficiency across a wide pH range and in complex water matrices, exhibiting excellent stability over multiple cycles, demonstrating strong potential for practical applications. This study provides an effective strategy for simultaneous Fe and N doping in sludge-derived biochar and offers mechanistic insights into Fe/N synergistic activation of PMS for practical water treatment. Full article

Cobalt-doped iron disulfide (FeS₂) thin films were synthesized via chemical bath deposition (CBD) followed by annealing at 450 °C, yielding phase-pure pyrite structures with multifunctional properties. A deposition temperature of 95 °C is critical for promoting Co incorporation, suppressing sulphur vacancies, and achieving structural stabilization of the film. After annealing, the dendritic morphologies transformed into compact quasi-spherical nanoparticles (~100 nm), which enhanced the crystallinity and optoelectronic performance of the films. The films exhibited strong absorption (>50%) in the visible and near-infrared regions and tunable direct bandgaps (1.14 to 0.96 eV, within the optimal range for single-junction solar cells. Electrical characterization revealed a fourth-order increase in conductivity after annealing (up to 4.78 Ω⁻¹ cm⁻¹) and confirmed stable p-type behavior associated with Co²⁺-induced acceptor states and defect passivation. These results demonstrate that CBD enabled the fabrication of Co-doped FeS₂ thin films with synergistic structural, electrical, and optical properties. The integration of earth-abundant elements and tunable electronic properties makes these films promising absorber materials for the next-generation photovoltaic devices. Full article

Background/Objectives: Exercise is essential for older adults to maintain or improve their physical condition. This study aimed to investigate whether improvements in physical performance, functional mobility, and balance through targeted physical function exercises could positively influence Concerns about Falling (CaF) and frailty in pre-frail community-dwelling older adults. Methods: We conducted an 18-month randomized controlled trial involving 112 pre-frail community-dwelling older adults aged 65 years or older. 55 individuals in the control group (CG) and 57 in the intervention group (IG) were assessed. The IG participated in a home-based physical function exercise program. Primary outcomes included Physical Performance (Short Physical Performance Battery, SPPB), Functional Mobility (Timed Up and Go, TUG), Balance (Berg Balance Scale, BBS), CaF (Falls Efficacy Scale–International, FES-I), and Frailty status (SHARE-FI). Assessments were conducted at baseline, 6, 12, and 18 months. Results: The IG showed significant improvements in BBS (p < 0.01, partial eta² 0.17), SPPB (p < 0.01, partial eta² 0.13), TUG (p < 0.01, partial eta² 0.14) and FES-I (p < 0.01, partial eta² 0.07) compared to the CG and their baseline after 6, 12 and 18 months of intervention. By 18 months, frailty status improved in the IG, with 12.3% classified as non-frail compared to 2.0% in the CG, while 14.5% of the CG transitioned to frailty versus none in the IG. Discussion: The intervention appears to support improvements in physical function and may contribute to reductions in CaF and beneficial changes in frailty status among pre-frail community-dwelling older adults. Full article

Gallic acid (GA) exhibits a broad range of biological activities; however, its clinical application is significantly limited by poor stability, rapid degradation, and low bioavailability. Consequently, developing responsive delivery platforms to enhance GA stability and targeted release has become an important research focus. Herein, GA was encapsulated within novel composite hydrogel beads (CMC-SA-Fe₃O₄@GA) prepared via crosslinking carboxymethyl chitosan (CMC) and sodium alginate (SA) with Fe₃O₄ nanoparticles (NPs) to facilitate efficient drug delivery. The formulation was characterized and evaluated in terms of drug-loading capacity, controlled-release properties, antioxidant activity, antibacterial performance, and biocompatibility. The results indicated that the GA loading efficiency reached 31.07 ± 1.23%. Application of an external magnetic field accelerated GA release, with the observed release kinetics fitting the Ritger–Peppas model. Furthermore, antioxidant capacity, evaluated by DPPH assays, demonstrated excellent antioxidant activity of the CMC-SA-Fe₃O₄@GA composite beads. Antibacterial tests confirmed sustained inhibitory effects against Escherichia coli and Staphylococcus aureus. In vitro, cellular assays indicated favorable biocompatibility with normal hepatic cells (HL-7702) and effective inhibition of hepatocellular carcinoma cells (HepG2). Overall, the novel pH- and magnetic field-responsive CMC-SA-Fe₃O₄@GA hydrogel system developed in this work offers considerable potential for controlled delivery of phenolic compounds, demonstrating promising applicability in biomedical and food-related fields. Full article

The activation of persulfate (PS) to oxidize and degrade 2,4-dichlorophenol (2,4-DCP) in aqueous solution represents a prevalent advanced oxidation technology. This study established a PS activation system using sulfide-modified nanoscale zero-valent iron supported on biochar (S-nZVI@BC). The optimal conditions included a PS:2,4-DCP mass ratio of 70:1 and S-nZVI@BC:PS of 1.5:1. The activator had excellent stability after being reused five times, which lead to high cost-effectiveness and sustainable usability. This system exhibited broad pH adaptability (3–11), with enhanced efficiency under acidic/neutral conditions. Chloride ion, nitrate, and carbonate had effects during the degradation. During the initial degradation phase, S-nZVI@BC played a primary role, with a greater contribution rate of adsorption than reduction. Fe⁰ played a dominant role in the PS activation process; reactive species—including HO•, SO₄•⁻, and O₂•⁻—were identified as key agents in subsequent degradation stages. The overall degradation processes comprised three distinct stages: dechlorination, ring-opening, and mineralization. Full article