Search Results (7,284)

With the rapid progression of global industrialization and urbanization, heavy metal contamination has emerged as a major global threat, especially cadmium pollution. Consequently, optimizing remediation measures has become a pivotal means to solve cadmium contamination. Compared to traditional physical and chemical remediation methods, microbial remediation has great potential in addressing cadmium pollution. In this study, a novel bacterial strain, Chryseobacterium sp. HGX-24, exhibiting high cadmium resistance was successfully isolated and screened from cadmium-contaminated environments. A preliminary discussion of the response mechanisms of this strain under cadmium stress is provided. Additionally, preliminarily explored the synergistic remediation of microbial-plant in cadmium-contaminated soil. Under conditions of high cadmium concentration, cadmium ions were effectively adsorbed by strain HGX-24 through extracellular polymers and functional groups on the cell wall surface, including −COOH, −CONH−, −NH, −OH, and >C=O. Extracellular proteins and polysaccharides were secreted by strain HGX-24 to regulate the adverse effects of heavy-metal cadmium ions on bacterial growth. Furthermore, the expression of genes such as antioxidant defense and ROS scavenging (katG, fabG, ybjT), Fe-S cluster assembly (sufB, sufD), sulfur metabolism (cysAU), amino acid metabolism (hisA, cysD, aspC), phenylacetic acid catabolism (paaC), and ribosomal proteins (rplC, rpsC, rpsL, rplA, rplY, rpmC) was regulated, affecting the synthesis and metabolism of membrane transporters (ABC transporters and efflux RND transporters), antioxidant enzymes (SOD, COT, POD), Fe-S clusters, thioredoxin family proteins, and ribosomal proteins, thereby enhancing resistance to cadmium toxicity. Moreover, strain HGX-24 was found to regulate the activities of redox enzymes in Zea mays L., thereby alleviating oxidative stress and reducing the negative feedback effects of reactive oxygen species in Z. mays. Full article

A 56-day feeding trial was conducted to evaluate the effects of varying dietary lipid and starch levels on growth performance, biochemical components, and hepatic glycolipid metabolism in hybrid grouper. Nine isonitrogenous diets were formulated to contain three levels of lipid (6%, 10%, or 14%) and starch (14%, 21%, or 28%) using a 3 × 3 factorial design. Juvenile fish (initial body weight: 19.06 ± 0.03 g) were randomly allocated to 27 floating net cages (25 fish per cage, three replicates per diet) in an indoor seawater recirculation system and hand-fed to apparent satiation twice daily. Two-way ANOVA was conducted to check treatment effects of dietary lipid and starch levels. No interaction effect between lipid and starch on growth and feed utilization was observed across all treatments; however, significant interactions between the two were observed for condition factor (CF), and some serum biochemical indicators and some hepatic glycolipid metabolic enzyme activities. Growth rate, specific growth rate, and feed efficiency (FE) exhibited a declining trend with increasing dietary lipid levels (p < 0.05). Conversely, hepatosomatic index (HSI), viscerosomatic index (VSI), condition factor, hepatic lipid and glycogen contents, muscle lipid content, serum triglyceride and high-density lipoprotein cholesterol contents, as well as hepatic carnitine palmitoyltransferase 1 (CPT-1) and lipoprotein lipase (LPL) activities, showed an increasing trend (p < 0.05). As lipid levels increased, serum total cholesterol (TC) and total protein (TP) contents dropped to a minimum at the intermediate lipid level (10%) and then rose, regardless of starch level. Hepatic fructose-1,6-bisphosphatase (FBP) activity increased significantly when lipid level rose from 6% to 10% (p < 0.05). With increasing dietary starch levels, HSI, VSI, hepatic and muscle glycogen contents, and serum low-density lipoprotein cholesterol content increased, while FE and serum TP content decreased (p < 0.05). Hepatic CPT-1, LPL, FBP, and pyruvate kinase activities were significantly enhanced when starch levels increased from 14% to 21% or 28% (p < 0.05). Serum aspartate aminotransferase activity was significantly higher in fish fed 14% lipid compared to those fed 6% or 10% lipid. These findings indicate that there is no interaction of dietary lipid and starch on growth and feed utilization, but high dietary lipid (14%) may enhance hepatic lipid oxidation while suppressing glycolysis, thereby limiting growth and promoting hepatic lipid deposition. The results provide a practical reference for optimizing dietary lipid and starch levels in cost-effective feed formulations for hybrid grouper. Full article

Dye-sensitized solar cells (DSSCs) remain attractive as low-cost photovoltaic devices; however, their practical efficiency is still constrained by electron-transport losses, interfacial recombination, and incomplete light harvesting in conventional titanium dioxide (TiO₂) photoanodes. The effects of TiO₂ film thickness, multi-walled carbon nanotube (MWCNT) incorporation, and multilayer oxide interface engineering on DSSC performance were examined. Degussa P25-TiO₂ photoanodes were first optimized with respect to thickness, after which controlled MWCNT loadings and sequential compact sol–gel TiO₂ and tin dioxide (SnO₂) sublayers were introduced. The optimum pristine P25-TiO₂ photoanode thickness was 9.11 μm, yielding an open-circuit voltage of 0.74 ± 0.01 V, a short-circuit current density of 14.10 ± 0.40 mA/cm², a fill factor of 56.24 ± 1.00%, and a power-conversion efficiency of 5.93 ± 0.20%. The incorporation of 0.025 wt% MWCNTs increased the efficiency to 6.04 ± 0.20%, corresponding to an absolute gain of 0.11 percentage points. The best performance was obtained with the sol–gel SnO₂/sol–gel TiO₂/P25-CNT multilayer photoanode, which delivered 0.74 ± 0.02 V, 16.22 ± 0.40 mA/cm², 57.59 ± 1.00%, and 6.89 ± 0.30%, respectively. FE-SEM, EIS, XRD, Heated Ultrasonic Cleaner and UV–visible analyses indicate that the multilayer architecture preserves porosity, enhances light harvesting, and suppresses interfacial recombination, while the CNT network facilitates charge transport. Full article

The rational design of oxygen carriers (OCs) is critical for enhancing biomass chemical looping gasification (BCLG) performance. This work systematically investigated the effects of different supports (Al₂O₃, ZrO₂, TiO₂, SiO₂) on the performance of NiFe-based OCs with oxidation and catalytic reforming functions. The gasification reactivity and support-active phase interaction of OCs in both oxidized and reduced states were evaluated. XRD, H₂-TPR, XPS, and SEM techniques were employed to characterize the phase composition, synergistic interactions, and surface morphology. The results showed that NiFeAl exhibited the optimal gasification performance in both oxidized and reduced states, achieving a syngas (H₂ + CO) yield of approximately 1.4 m³/kg (dry walnut shell). NiFeAl featured a higher Fe binding energy, abundant cavity structures, and the uniform dispersion of Ni and Fe on Al₂O₃, which confirm the formation of an appropriately strong Ni-Fe-Al ternary system. In contrast, NiFeZr suffered from the higher CO₂ yield, attributed to the over-oxidation caused by the weak interactions. NiFeTi and NiFeSi had lower syngas yields due to their poor reducibility induced by excessively strong interactions. This work verifies that moderate support-active phase interactions in OCs are optimal for BCLG. Full article

This work examines the influence of the Ce/Fe ratio in Pt/CeO₂-Fe₂O₃ catalysts on the peculiarities of metal–support interaction and catalytic properties in the total oxidation of toluene. The physical-chemical properties of the Pt/CeO₂-Fe₂O₃ catalysts are studied using low-temperature N₂ adsorption–desorption, XRD, TPR-H₂, Raman, and TEM. The citrate method to synthesize the mixed CeO₂-Fe₂O₃ supports makes it possible to obtain dispersed defective oxide particles that actively interact with the supported Pt species. An increase in the oxygen mobility of CeO₂-Fe₂O₃ after the Pt deposition and the cooperation of active oxidative species with the active site of Pt is a key to the catalytic activity in the total oxidation of toluene. This effect is the highest for the Pt/3Ce2Fe catalyst, and the temperature of 50% toluene conversion over this catalyst is 167 °C. Full article

Iron-based nanoparticles, particularly iron oxide nanostructures (IONPs), have emerged as versatile and clinically relevant platforms for drug delivery and theranostic applications. Among these, superparamagnetic iron oxide nanoparticles (SPIONs), including magnetite (Fe₃O₄) and maghemite (γ-Fe₂O₃), are the most extensively investigated due to their biocompatibility, magnetic responsiveness, and established safety profiles. Their unique superparamagnetic behavior enables external magnetic-field-guided targeting, magnetic resonance imaging (MRI) contrast enhancement, and magnetically triggered hyperthermia, enabling simultaneous diagnosis and therapy. Surface functionalization with polymers, silica, lipids, peptides, and biomolecules further improves colloidal stability, circulation time, targeting specificity, and controlled drug release. Core–shell architectures and multifunctional hybrid systems have expanded the therapeutic scope of iron nanoparticles, integrating chemotherapy, gene delivery, photothermal therapy, and Fenton reaction–mediated catalytic therapy. Despite promising preclinical outcomes, challenges remain regarding long-term biosafety, oxidative stress induction, biodistribution, large-scale reproducibility, and regulatory translation. This review summarizes the physicochemical properties, synthesis strategies, surface-engineering approaches, drug-loading mechanisms, and biomedical applications of iron-based nanoparticles, highlighting recent advances in multifunctional and peptide-functionalized systems. Critical considerations for clinical translation and future perspectives in precision nanomedicine are also discussed. Full article

Inking disorder is a peach quality defect in which fruits manifest a dark epidermis discoloration; this disorder reduces the commercial value of peach fruits. In red pigmented peach fruit, it has been proposed that inking is associated with mechanical damage and reactions involving metal ions (Fe, Cu, and Zn) and anthocyanins, but in yellow peach cultivars inking mechanism is unknown. The objective of the present investigation was to evaluate the effect of mechanical damage and contamination with Fe metal ions in the development of inking disorder in three yellow peach cultivars. The present study revealed that Fe₂(SO₄)₃ application increased total phenolic content and chlorogenic acid levels in all cultivars but did not induce inking symptoms in the absence of mechanical damage. In contrast, brushing treatments triggered inking development in ‘Colegio’ and ‘MG8’, allowing differentiation of cultivar susceptibility, whereas ‘229’ showed complete resistance. Mechanical damage also significantly increased phenolic compounds, as well as phenylalanine ammonia-lyase (PAL) and polyphenol oxidase (PPO) activities, with higher levels consistently observed in susceptible cultivars. Notably, the severity of inking increased when mechanical damage was combined with Fe(III) application. These results indicate that inking development requires both phenolic accumulation and their enzymatic oxidation. Fe(III) ions act as an enhancing factor by stimulating phenolic biosynthesis, thereby intensifying discoloration. The resistance observed in cv. ‘229’ is associated with lower phenolic synthesis and oxidative activity. This study provides new insights into the physiological mechanisms of inking in yellow peaches and offers practical implications for postharvest management and cultivar selection. Full article

The present work investigated the thermodynamic behaviors of oxygen in a liquid Fe–Ti alloy over a wide Ti concentration range of 11.6–71.2 wt% at 1873 K by integrating equilibrium experiments with thermodynamic modeling. To prevent excessive oxidation during the equilibrium experiments, the liquid alloys were equilibrated in a purified Ar atmosphere with an oxygen partial pressure below ~10⁻²⁰ atm. Two quenching methods—furnace quenching with He gas injection and water quenching via quartz tube suction—were employed to evaluate the effect of cooling rate on total oxygen measurements. While He gas quenching led to higher measured oxygen contents owing to the formation of secondary Ti oxides, the quartz tube suction quenching method consistently yielded significantly lower oxygen values. The dissolved oxygen content increased with increasing Ti content. Electron probe microanalysis identified TiO as a stable equilibrium oxide phase above 11.6 wt% Ti, which was characterized as a face-centered cubic (FCC) rock-salt structure via electron backscatter diffraction analysis. Based on these results, a thermodynamic assessment of oxygen behavior in a liquid Fe–Ti alloy in equilibrium with TiO was performed for the first time using a modified quasichemical model. Consequently, the present model successfully reproduced the Ti–O relationship in the liquid Fe–Ti alloy across both the high-Ti concentration region saturated with TiO and the low-Ti concentration region saturated with Ti₂O₃ and Ti₃O₅. Full article

A nanostructured sensing platform based on electrospun functionalized multi-walled carbon nanotubes/poly(3-aminobenzylamine) (FMWCNTs/P3ABA) was developed for the electrochemical detection of dopamine (DA) on fluorine-doped tin oxide (FTO) glass substrate. The electrochemical characteristics of the electrodes were investigated by chronocoulometry (CC) and cyclic voltammetry (CV) in phosphate-buffered saline solution containing K₃[Fe(CN)₆] as a redox mediator. The zeta potential analysis confirmed the presence of a stable surface charge that favors electrostatic interaction with DA molecules. The DA detection was performed in human urine by differential pulse voltammetry (DPV) over a potential of −0.2 to 0.8 V and at scan rate of 5 mV s⁻¹, where the FMWCNTs/P3ABA nanofiber electrode exhibited a high sensitivity of 1.502 µA cm⁻² nM⁻¹, a linear detection range of 10–500 nM (R² = 0.992), and a limit of detection of 1.753 nM. The sensor exhibited stable and reproducible responses, and the fibrous composite effectively discriminated DA from common electroactive interferents, including ascorbic acid, uric acid, creatinine, and glucose. Furthermore, reliable dopamine quantification in human urine samples demonstrates the strong potential of the electrospun FMWCNTs/P3ABA composite nanofiber platform for practical bioanalytical and non-invasive sensing applications in the future. Full article

The rising global demand for lithium has led to substantial accumulation of lithium slag, a by-product of lithium carbonate production and a potential environmental contaminant. Leachates from this material contain various metal elements and may pose risks to ecosystems and organismal health. However, research on its neurotoxicity and underlying mechanisms remains limited. In this study, zebrafish embryos at 6 h post-fertilisation were exposed to varying concentrations of lithium slag leachate for 7 days. The leachate contained multiple metal ions (Li, Fe, Mn, Ni, Zn, As, Cr, Cu, Hg, Cd, Pb, etc.). Following exposure, significant metal accumulation was observed in larvae, accompanied by developmental malformations (yolk sac oedema, cardiac haemorrhage, and uninflated swim bladders). Behavioural assessment revealed reduced swimming distance and velocity, along with disrupted circadian rhythms. Biochemical analyses showed elevated Reactive oxygen species (ROS), Superoxide dismutase (SOD), Catalase (CAT), and Malondialdehyde (MDA), alongside decreased Glutathione (GSH), indicating oxidative stress. Transcriptomic analysis confirmed downregulation of core circadian genes. Neurotransmitter assays revealed decreased acetylcholine (Ach), noradrenaline (NE), and dopamine (DA), with increased gamma-aminobutyric acid (GABA) and serotonin (5-HT). These findings demonstrate that lithium slag leachate induces oxidative stress, circadian disruption, and neurobehavioural toxicity in zebrafish, providing important evidence for environmental risk assessment. Full article

The peripheries of rare-metal metallogenic systems frequently host skarn-type or hydrothermal vein-type Pb-Zn deposits, though their genetic connections with parental systems remain debated. The newly identified Gariatong W-Mo polymetallic metallogenic system in the Lhasa Terrane displays well-defined Nb-Ta-Rb, Mo-W, W-Mo, W-Bi, and Pb-Zn-Ag metallogenic zoning, establishing it as an exemplary site for investigating genetic relationships between Pb-Zn and rare-metal mineralization. This investigation targets skarn-type Pb-Zn deposits spatially associated with rare-metal orebodies at Gariatong, utilizing integrated analytical approaches, including in situ LA-ICP-MS trace-element analysis of sulfides, sulfur isotope geochemistry, and LA-ICP-MS elemental mapping of sphalerite, to constrain metal sources, characterize fluid evolution, and establish genetic correlations with the rare-metal system. Key findings include the following: (1) sphalerite shows enrichment in Fe, Mn, Co, and Cd, while pyrite contains elevated As, Pb, Co, Cu, and Mn. Fe, Cd, and Mn primarily occur as solid solutions or nanoparticles, whereas As and Pb exist as micro-inclusions. (2) Sphalerite Zn/Cd ratios (73.6–184) and Co-Ni-As ternary diagrams confirm a magmatic–hydrothermal skarn origin. (3) Mineralization occurred under moderate-temperature, mildly oxidized conditions, as constrained by sphalerite Fe contents and mineral assemblages. Sulfur isotope compositions (δ³⁴S = −1.0‰ to 3.2‰; mean: 1.9‰) indicate a magmatic sulfur source. This study reveals that the Nb-Ta-Rb mineralization, quartz-vein- and greisen-type W-Mo deposits, and skarn-type Pb-Zn orebodies—all genetically associated with highly fractionated granites—constitute an integrated magmatic–hydrothermal system with vertical (depth-related) zoning relative to the granitic intrusion. These results provide critical constraints for understanding rare-metal–Pb-Zn genetic associations and suggest that Pb-Zn mineralization may serve as a key exploration indicator for rare metals in the Lhasa Terrane. Full article

Surface discharge-induced degradation poses a significant threat to the operational reliability of high-voltage insulation systems. This research investigates the dielectric endurance of polyester-based nanocomposites reinforced with seven distinct nano-additives: iron oxide (Fe₃O₄), copper oxide (CuO), titanium oxide (TiO₂), aluminum oxide (Al₂O₃), silicon dioxide (SiO₂), zinc borate (ZnB) and graphene oxide (GO). Specimens were fabricated at 0.5% and 0.75% weight concentrations and subjected to constant AC electrical stress of 4.5 kV at 50 Hz until failure using the first-plane tracking method. To accurately monitor the aging process, a sophisticated signal processing framework involving Hankel-matrix-enhanced Robust Principal Component Analysis (RPCA) was developed to extract high-frequency discharge features from captured leakage current signals. The degradation characteristics were quantified using various statistical metrics, including Kurtosis, RMS and Burst Discharge Index (BDI). Experimental findings demonstrate that the incorporation of nanoparticles significantly extends the time-to-failure compared to neat polyester, although the effectiveness is highly dependent on both additive type and concentration. At 0.5 wt.%, ZnB exhibited the superior performance in delaying carbonized track formation. However, at 0.75 wt.%, Al₂O₃ emerged as the most effective additive, achieving a maximum endurance time of 31.61 min. In contrast, certain additives like TiO₂ showed a performance decline at higher loadings, likely due to nanoparticle agglomeration. The Hankel-RPCA methodology successfully isolated discharge-specific signatures from background noise, establishing a strong correlation between signal features and material failure stages. This study confirms that the synergy between advanced nanomaterial modification and robust signal processing provides an effective diagnostic tool for monitoring insulation health, offering a vital pathway for the designing of high-performance dielectrics for real-world power system applications. Full article

The microstructure, phase composition, and high-temperature oxidation behavior of Al_0.5CoCr_0.5NiPt_0.1 and AlCoCr_0.5NiPt_0.1 multi-principal element alloys (MPEAs) at 1100 °C in air were investigated. Depending on the content of aluminum, the microstructure of as-cast samples contains FCC and BCC solid solutions. Similarly, the ratio of two solid solutions varies depending on the aluminum content in the alloy. When the content of aluminum is x = 0.5, the microstructure is dominated by the FCC solid solution, while a BCC solid solution is dominated when the concentration of aluminum is increased to x = 1.0. Moreover, in both MPEAs, platinum exists as a part of solid solutions rather than a separate phase. High-temperature oxidation was carried out in a Plavka.Pro PM-1 SmartKiln muffle furnace under isothermal conditions at 1100 °C for 100 h exposure in air, and weighing was performed every 10 h. The maximum specific weight gain for the Al_0.5CoCr_0.5NiPt_0.1 alloy was 0.965 mg/cm², and 0.675 mg/cm² for the AlCoCr_0.5NiPt_0.1 alloy. Based on the high-temperature oxidation experiment results, it was established that AlCoCr_0.5NiPt_0.1 MPEA exhibits greater resistance towards high-temperature dry air corrosion with the formation of an exclusive Al₂O₃ scale on the surface with 3–5 μm thickness; the parabolic oxidation rate constant for this alloy is k_p = 20.2 × 10^–13 (g²/cm⁴s). Introduction of platinum into the composition of the Fe-free AlCoCr_0.5Ni alloy reduces the value of the parabolic oxidation rate constant by half. Full article

Arsenic (As) contamination in groundwater represents a critical global environmental health issue. The reductive dissolution of arsenic-bearing iron oxides by dissimilatory metal-reducing bacteria (DMRB) is a key biogeochemical process driving arsenic mobilization and release in groundwater. However, the mechanism of exogenous electron shuttles in this process remains poorly understood. This study investigated the impact of the quinone-based electron shuttle anthraquinone-2,6-disulfonate (AQDS) on the reductive dissolution of arsenic-loaded goethite by the model DMRB Shewanella putrefaciens CN32 (S.P CN32). The mobilization and transformation behaviors of arsenic and iron were compared under different pH conditions and using different arsenic-loading methods (coprecipitation vs. adsorption). Results demonstrated that AQDS acted as an electron transfer mediator. It significantly enhanced the reductive dissolution of Fe(III). It also significantly enhanced the reduction of As(V). These actions collectively accelerated arsenic release and mobilization. The study also revealed a competitive preferential order in microbial reduction, where the thermodynamically more favorable Fe(III) reduction preceded As(V) reduction. Environmental pH co-regulated this process. Its influence worked through microbial activity and mineral surface properties. A neutral pH was most conducive to the AQDS-mediated bioreduction of arsenic and iron. This study elucidates the critical role of electron shuttles in the biogeochemical cycling of arsenic in contaminated sites, providing a scientific basis for a deeper understanding of the formation mechanisms and risk assessment of high-arsenic groundwater. Full article

Synthetic dyes frequently persist through conventional wastewater treatment, motivating the use of advanced oxidation processes capable of breaking down these stable molecules. Metal-doped carbon dots (CDs) offer a tuneable platform for catalytic dye degradation in water, although their performance varies strongly with operating conditions. The aim of this work was to determine how temperature, H₂O₂ dosage, and pH influence the catalytic behaviour of Fe-, Cu-, Zn-, and Mg-doped CDs during the degradation of methylene blue (MB) and rhodamine B (RB), optimised using a Taguchi L27 orthogonal array design. Temperature and oxidant loading were the dominant factors: higher temperatures accelerated reactions through Arrhenius-type kinetics, while increasing H₂O₂ availability improved removal until excessive levels began to suppress •OH generation. Across all condition sets, apparent rate constants spanned 7.0 × 10⁻⁴–2.65 × 10⁻² min⁻¹, with t₅₀ values of 26–217 min and t₉₀ extending from ~86 min to >700 min; final decolourisation ranged from ~17% to nearly 100%. pH played a secondary role, mainly affecting dye speciation and surface adsorption. Dopant identity shifted the optimum operating region for each catalyst: Fe- and Cu-CDs achieved complete or near-complete removal of both dyes at pH 7 and 50 °C with relatively low H₂O₂ dosage (0.5–1.0 mL); Zn-CDs reached equivalent performance at pH 7 and 25 °C but required higher oxidant loading (1.5 mL of H₂O₂), reflecting their photo-induced rather than thermally driven activation mechanism; Mg-CDs performed comparably under the same conditions as Fe- and Cu-CDs. The resulting condition–catalyst map highlights the operating regimes that maximise efficiency while minimising chemical input, providing a practical framework for selecting carbon-dot-based catalysts for water treatment applications. Full article