Search Results (130)

Schizophrenia is a heterogeneous neurodevelopmental disorder in which genetic liability, developmental exposures, illness stage, treatment, and metabolic or inflammatory comorbidity may shape redox biology. This narrative review evaluates the human and mechanistic evidence for impaired redox adaptation as a convergence mechanism linking glutathione (GSH) regulation, N-methyl-D-aspartate receptor hypofunction, parvalbumin-interneuron and perineuronal-net vulnerability, mitochondrial–glial dysfunction, and neuroimmune signalling. The findings do not support a uniform oxidative abnormality across all patients or compartments: the peripheral biomarkers are heterogeneous, the group-level brain GSH magnetic resonance spectroscopy findings are largely null, and treatment-related changes vary by marker and illness phase. Beyond the established GSH–NMDA–redox–immune models, we integrate iron–lipid redox regulation as a conditional, hypothesis-generating extension and apply a deliberately conservative evidence hierarchy. Human studies more often report a lower peripheral iron and reduced or redistributed brain iron than a uniform iron excess; the plasma signals for predominantly intracellular proteins remain analytically unvalidated, and ferroptotic neuronal death has not been demonstrated. Longitudinal, sex-aware, multi-compartment, and challenge-based studies are needed to define meaningful redox subgroups; no redox- or ferroptosis-related biomarker is currently validated to guide treatment selection. Full article

Ce-modified MnCo₂O₄ flower-like nanosheet electrodes were prepared on nickel foam by a hydrothermal-calcination route and sequentially optimized with respect to reaction time, nominal Ce content, and PVP addition. Comparative SEM, XRD, XPS, and N₂-sorption analyses identify MnCo₂O₄-9 h-3%Ce-PVP as the optimized electrode, with an open hierarchical nanosheet network and a BET surface area of 210.0 m² g⁻¹. The direct XRD/XPS control comparison distinguishes Ce-associated lattice and surface-state changes from PVP-associated synthesis effects without treating either trend as proof of substitutional Ce occupancy or quantitatively established oxygen vacancies. Likewise, PVP is treated as a morphology-directing additive whose transient adsorption or bridging role remains a synthesis hypothesis rather than a directly verified molecular mechanism. The optimized positive electrode delivers 2008 F g⁻¹ at 1 A g⁻¹, retains 1227 F g⁻¹ at 20 A g⁻¹, and shows 99.0% capacitance retention after 10,000 cycles at 5 A g⁻¹. A carbon-supported iron oxide negative electrode, designated C/Fe₂O₃ only as a sample label because its exact oxide phase was not independently resolved by XRD or Raman spectroscopy, provides 443 F g⁻¹ at 1 A g⁻¹. The resulting charge-balanced asymmetric device operates over 0–1.6 V and delivers 34.6 F g⁻¹ at 1 A g⁻¹, corresponding to 12.30 Wh kg⁻¹ at 0.8 kW kg⁻¹. At 10 A g⁻¹, it retains 29.8 F g⁻¹ and delivers 10.60 Wh kg⁻¹ at 8.0 kW kg⁻¹, equivalent to 86.1% capacitance retention over a tenfold increase in current density. All device-level gravimetric values are calculated using the total active mass of both electrodes. Full article

Co–Mg–Fe oxide systems are promising candidates for thermally stable deep oxidation catalysts because they potentially combine redox-active cobalt and iron components with stabilizing magnesium-containing phases. In this work, phase formation in a Co–Mg–Fe oxide system obtained by thermal decomposition of nitrate precursors with a Co:Mg:Fe ratio of 1:1:1 was studied over a wide range of heat-treatment temperatures from 400 to 1300 °C. The samples were characterized by X-ray diffraction, Mössbauer spectroscopy, Fourier-transform infrared spectroscopy, scanning electron microscopy with energy-dispersive X-ray spectroscopy mapping, and temperature-programmed oxygen desorption. The results show that the system undergoes staged phase evolution. At 400 °C, α-Fe₂O₃, including Mg-modified hematite-like states, cobalt-containing spinel phases, and a rocksalt oxide phase, is formed. Starting from 550 °C, a mixed ferrite spinel phase appears and its content increases with temperature. The transition through 800–900 °C is accompanied by decomposition of cobalt-containing spinels, a sharp change in the inversion parameter of the mixed ferrite, and formation of a stable high-temperature combination of ferrite spinel and rocksalt oxide solid solution. Oxygen desorption is most pronounced for the low- and medium-temperature samples and decreases strongly after high-temperature treatment. The obtained results provide the basis for the design of thermally stable Co–Mg–Fe oxide catalysts for deep oxidation processes. Full article

This study reports the synthesis of low-defect Prussian blue analogues (PBAs) using a single iron-source method and systematically investigates the influence of atmospheric components, particularly water and oxygen, on their oxidative decomposition. Our findings demonstrate that the oxidative degradation of PBAs is governed synergistically by moisture and oxygen, with ambient humidity identified as the primary factor determining both the extent and kinetics of their decomposition. Notably, a pure oxygen environment by itself does not trigger material degradation, while oxygen markedly accelerates the decomposition only in the presence of moisture. As a result of the oxidation, enhanced Coulombic interaction between sodium ions and cyano groups induces structural modifications in the lattice framework, driving a phase transformation from monoclinic to cubic symmetry, accompanied by changes in its unit cell volume. Furthermore, in high-humidity environments, atmospheric moisture promotes the gradual deintercalation of sodium ions from the Prussian blue framework, resulting in the conversion of sodium-rich Prussian blue to the sodium-deficient form. Concurrently, an increase in lattice defect density leads to partial structural collapse, inducing the release of free ferrocyanide ions, which may subsequently react with the deintercalated sodium ions to form the sodium ferrocyanide impurity phase. We also find that the preferential decomposition of low-spin iron over high-spin iron within the framework leads to a further reduction in its electrochemical capacity. In contrast, potassium Prussian blue exhibits minimal interaction with water molecules and can effectively repel them through steric hindrance. Therefore, partial substitution of sodium with potassium ions is proposed as a viable strategy to enhance the structural stability of the Prussian blue framework, improve the storage performance of sodium Prussian blue (NaPB), and mitigate water ingress. This work offers fundamental insights into the storage characteristics and oxidative degradation mechanisms of PBAs. Full article

Fresh flotation tailings represent an underutilized archive of mineralogical and geochemical information in which multiple strands of evidence for ore-forming processes and post-depositional modification can be preserved. Detailed characterization of tailings is also vital for assessment of their future potential as a secondary source of recoverable by-products. This study investigates residual mineral speciation and mineral distributions in size fractions of tailings from the Prominent Hill iron oxide–copper–gold (IOCG) deposit, South Australia, with emphasis on rare earth element (REE) minerals and associated phases containing uranium (U). Assemblages of REE minerals can be highly complex at the micron scale and include sequences of mineral replacement, notably monazite → florencite, and monazite → synchysite. Bastnäsite-(Ce) commonly appears paragenetically early and is frequently altered or replaced by synchysite and parisite, supporting episodes of REE remobilization and reconcentration over geological time. Uranium is closely associated with REEs, and U-mineral assemblages are similarly characterized by intricate replacement relationships between uraninite and secondary phases. Uraninite is variably replaced by coffinite and the U-carbonate wyartite, reflecting changes in redox state, silica activity, and fluid composition. Additional replacement pathways from uraninite to Cu–Fe sulphides, including bornite and chalcopyrite, are documented and indicate coupled dissolution–reprecipitation of sulphides and U-minerals during superimposed hydrothermal activity. Preservation of mineralogical relationships within tailings drawn from multiple parts of a large deposit highlights their value as an essentially untapped library of information to reconstruct deposit evolution, complementing traditional study of selected drill core samples. Systematic investigation of tailings from large deposits can improve genetic models for large copper deposits, including but not restricted to IOCGs, and provide essential insights into REE behaviour, uranium remobilization, and critical metal potential. These findings emphasize the scientific and economic value of tailings-based studies for improved resource characterization, refining metallogenic interpretations, guiding future exploration strategies, and assessing opportunities for reprocessing and metal recovery in large ore systems worldwide across diverse geological settings. Full article

This study evaluated Palmaria palmata hydrolysates produced using Alcalase^® and Flavourzyme^® at 1, 2, 3, 4, 5, and 10% (w/w biomass protein, corresponding to AF1-10), and their performance in oil-in-water nanoemulsions under iron-induced oxidation. AF4 showed significantly higher total amino acid and phenolic contents and the strongest Fe²⁺-chelating activity (IC₅₀ = 1.64 ± 0.22 mg/mL, p < 0.05) and was therefore selected for nanoemulsion stabilization. Nanoemulsions exhibited high physical stability with no significant changes in droplet sizes (D_3,2 ~77–79 nm), ζ-potential (~−18 to −19 mV), and viscosity (~1.2–1.5 cP) (p > 0.05). Dynamic interfacial tension measurements and confocal laser scanning microscopy (CLSM) indicated limited interfacial activity of AF4, with most components remaining in aqueous phase. Compared to the control, AF4 significantly reduced peroxide formation (~100–164 vs. 289–357 meq/kg at Day 4–8, p < 0.05) and partially preserved tocopherols. It also delayed the formation of some volatiles during intermediate stages of storage. However, it was less effective than ethylenediaminetetraacetic acid (EDTA). Increasing the AF4 concentration did not further improve oxidative stability. These findings suggest that antioxidant efficacy depends on composition, interfacial behavior, and spatial distribution. Antioxidants with limited interfacial activity may therefore exhibit different modes of action within emulsified systems. Full article

Insufficient oxidative capacity can limit humification during municipal sludge composting. This study comparatively evaluated two Fenton-like amendment systems, a homogeneous copper-based treatment (CH) and a heterogeneous nano-iron-based treatment (NFH), for their effects on composting performance, humification-related indices, spectroscopic characteristics, and bacterial community succession. Both amended treatments improved composting performance relative to the control, reaching higher peak temperatures (68.5 °C for CH and 70.3 °C for NFH) and prolonging the thermophilic phase. NFH also showed stronger moisture removal, with the final moisture content decreasing to 58.1%, compared with 65.1% in CH and 64.1% in the control. CH showed the highest apparent humic acid accumulation (1173 mg kg⁻¹), whereas NFH exhibited spectroscopic features commonly associated with lower E₄/E₆ ratios and more pronounced humic-like fluorescence characteristics. Ultraviolet–visible spectroscopy (UV–Vis), Fourier transform infrared spectroscopy (FTIR), and excitation–emission matrix fluorescence spectroscopy (EEM) analyses collectively indicated progressive transformation toward more aromatic and humified organic matter in the amended treatments. Bacterial community succession also differed across treatments, and several enriched taxa, including Rhodanobacter and Thermobifida, showed positive associations with reactive oxygen species (ROS)-related variables and humification indices. These results describe treatment-linked dynamics in humification and suggest corresponding changes in microbial succession during sludge composting, with potential implications for process outcomes. Full article

Alzheimer’s disease (AD) research has primarily focused on amyloid beta (Aβ) and tau protein; however, drug development targeting these two proteins has been disappointing. Therefore, there is an urgent need to explore the novel pathogenic mechanisms underlying AD. Recently, we found that expression of the K670N/M671L-mutated amyloid precursor protein (APP) in 293T cells significantly reduced membrane ferroportin (FPN) levels. Furthermore, 2-month-old APP/PS1 mice exhibited a marked decrease in membrane FPN levels, while total FPN expression and Aβ levels remained unchanged. Further studies revealed that features of ferroptosis were present in the brains of 2-month-old APP/PS1 mice, and that treatment with ferroptosis inhibitors or iron chelation significantly alleviated early pathological changes and cognitive impairment in these animals. In addition, supplementation with an APP–FPN binding peptide during the early phase ameliorated AD-related pathologies, including Aβ deposition, neuroinflammation, oxidative stress, and synapse-associated protein deficits, in APP/PS1 mice. Collectively, our findings suggest that APP mutations may contribute to early brain pathological changes and subsequent memory impairment in AD by downregulating membrane trafficking of FPN and inducing ferroptosis, thereby providing new molecular targets for drug development. Full article

In this study, commercial Ospray-2507 super-duplex stainless steel powder was investigated for the first time as a potential metal support material for solid oxide cells. Initially, metal supports were fabricated and processed in air using various sintering profiles, followed by comprehensive mechanical, structural and electrochemical characterization. The optimal sintering condition was identified as 900 °C for 5 h. Subsequently, sintering under a H₂ atmosphere was explored, and its effects on the microstructural and functional properties of the metal supports were systematically to assessed to evaluate the influence of the sintering atmosphere on material performance. Although X-ray diffraction patterns showed no phase changes between the two sintering atmospheres, notable improvements were observed in mechanical, electrochemical, and microstructural properties under H₂ sintering. XPS spectra reveal that both air- and hydrogen-treated surfaces remain rich in chromium (Cr) and Manganese (Mn), which together dominate the surface and consequently attenuate the signal from the underlying iron. The thickness of the Cr- and Mn-based oxide layer decreases when sintering MS in H₂ atmosphere. Specifically, mechanical strength, as measured by three-point bending tests, increased by a factor of 12.5, and hardness rose from 500.3 to 523.5 HV. Furthermore, electrical conductivity also improved significantly, exhibiting an approximately 2.3–2.4 fold increase under H₂-sintered conditions. Full article

The increasing demand for environmentally benign inorganic pigments has stimulated interest in sustainable synthesis routes for iron oxide nanoparticles that minimize toxic reagents and energy-intensive processing. In this study, a plant-mediated approach for the synthesis of hematite (α-Fe₂O₃) nanoparticles using Spinacia oleracea (spinach) leaf extract is presented, with particular emphasis on pigment-relevant material characteristics. An aqueous spinach extract was employed as a natural reducing and stabilizing medium for ferric ions under ambient conditions. The formation of iron oxide nanoparticles was indicated by a characteristic color change and confirmed by structural and morphological characterization. X-ray diffraction revealed phase-pure crystalline hematite, while transmission electron microscopy showed quasi-spherical nanoparticles with sizes in the range of 20–50 nm. The synthesis avoids hazardous chemicals, high-temperature calcination, and organic solvents, offering a low-energy and environmentally compatible route. Although the yield per batch is modest, the simplicity, non-toxicity, and pigment-suitable properties of the synthesized nanoparticles highlight the potential of this method for sustainable pigment and coating applications. Full article

Iron powder represents a promising carbon-free, sustainable fuel, yet its practical utilisation in combustion has not yet been realised. Achieving stable, efficient iron-only flames is challenging, and the environmental impact of hybrid iron-hydrocarbon combustion, including particle emissions, is not fully understood. This study investigates hybrid methane–iron powder flames to assess iron’s role in modifying gas and particle phase emissions and its potential as a sustainable energy carrier. The combustion of iron was investigated at both the single particle and powder flow scales. Experimental diagnostics combined high-speed and microscopic imaging, ex situ particle sizing, in situ gas analysis, and aerosol measurements using an Aerodynamic Particle Sizer (APS™) and a Scanning Mobility Particle Sizer (SMPS™). For single particle combustion, high-speed imaging revealed rapid particle heating, oxide shell growth, cavity formation, micro-explosions, and nanoparticle release. For powder combustion, at 0.5 g/min and 1.26 g/min, the experiment yielded oxidation fractions of 15.15% and 23.43%, respectively, and increased CO₂ emissions by 0.22–0.35 vol% relative to methane–air flames, while NOx changes were negligible. Aerosol analysis showed a supermicron mode at ~2 µm and submicron ultrafine particles of 89% <100 nm with a modal diameter of ~56 nm. The observed ultrafine particle emissions highlight the need to evaluate health, material-loss, and fuel-recycling implications. Burner optimisation or premixed strategies could reduce CO₂ emissions while enhancing iron oxidation efficiency. Full article

Iron oxides are crucial for the long-term storage of soil organic carbon (SOC) in paddy soils, making them a key factor in global carbon cycles and important for strategies aimed at combating climate change. This review examines the role of iron oxides in paddy soils, particularly their interaction with SOC, which helps stabilize carbon and contributes to mitigating climate change. These processes of iron oxide phase transformations, wet–dry cycles, and microbial activity help trap carbon in the soil, supporting climate change mitigation efforts. Wet–dry cycles promote mineral dissolution and re-precipitation, forming new reactive surfaces and OC-Fe complexes. Future research should adopt a multi-scale approach to better connect molecular mechanisms with ecosystem-level carbon processes. A deeper understanding of iron oxide behavior in paddy soils will support the development of sustainable soil management practices and improve models for predicting soil carbon sequestration under climate change. Full article

This study investigates ceramic bricks produced by partially replacing clay with Pb–Zn metallurgical residues (lead furnace dust and cyclone dust), fly ash, and carbonaceous additives. The novelty lies in the integrated multi-waste formulation and the combined FTIR–TGA–XRD analytical approach used to elucidate phase-formation mechanisms. The results show that firing promotes the development of quartz, mullite, iron oxides, and an extensive Fe–Pb–Zn–Si–O amorphous network, while higher residue contents enhance amorphization and suppress mullite crystallization. These microstructural changes correlate with reduced compressive strength (1.6–3.1 MPa) and high water absorption (32–36%), although all samples completed 15 freeze–thaw cycles. Heavy-metal leaching assessed by atomic absorption spectroscopy (AAS) revealed very low Pb (0.08–0.20 mg/L) and Zn (0.25–0.45 mg/L) release, well below international safety limits, demonstrating effective immobilization of hazardous ions within the glassy matrix. Overall, the study provides new insight into multi-waste interactions during sintering and confirms that controlled residue incorporation enables environmentally safe, non-load-bearing ceramic materials with reduced clay consumption. Full article

This research constitutes a novel experimental approach to valorizing an industrial by-product: the ‘brick’. Studies put emphasis on the importance of detailed structural characterization of brickminerals and their chemical evolution upon heating, contributing rationally to the design and development of new glass–ceramic forms that would be suitable for efficiently encapsulating radio-nuclides. The brick used is a complex material composed of metakaolinite, illite, sand and impurities such as rutile and iron oxides/hydroxides. Raw brick was first activated with a range of sodium hydroxide concentrations, and, second, cured at different temperatures from 90 °C to 1200 °C. Alkali-brick frameworks gradually decomposed during the firing, and turned into crystalline ceramic phases (analcime and leucite) embedded inside an amorphous silica-rich phase. After each heating stage, the cured-brick sample was exhaustively characterized by using a variety of advanced analytical techniques, including powder X-ray diffraction, ESEM/EDS microscopy and ²⁹Si-²⁷Al-MAS-NMR spectroscopy. Ultra-high magnetic field NMR (28.2 T) was used to distinguish and quantify Al(IV), Al(V) and Al(VI) configurations, and to better follow distinctive changes in ²⁷Al environments of brickminerals under thermal effects. Glass-ceramized brick exhibited high specific density (~2.6 g·cm⁻³), high compactness and good corrosion resistance under static, mild and aggressive conditions, attesting to its high solidification and chemical durability. Full article

Modification of zeolitic structures through the incorporation of transition metal oxides has proven to be a promising approach for heterogeneous catalysis. In the present study, *BEA zeolite was modified using the incipient wetness impregnation method with varying amounts (10, 20, and 40 wt.%) of iron(III) oxide to investigate its structural and physicochemical properties. Characterization techniques such as XRD, UV–Vis DRS, FT–IR, Raman spectroscopy, SEM/EDS, TEM/EDS, and SAED, as well as textural and thermal analyses, were employed to assess the main changes. Different iron species were detected, including isolated iron(III) and well-dispersed Fe₂O₃ nanoparticles coating the zeolite surface. Under the synthesis conditions, increased Fe₂O₃ loading promoted hematite nanocrystal growth and the formation of the α-Fe₂O₃ phase, as demonstrated by XRD, Raman, and SAED analyses. Key observations included the preservation of the zeolite framework, high relative crystallinity (ranging from 70% to 85%), and a band gap of approximately 2.0 eV. Furthermore, a general increase in mesoporosity and external surface area was observed, along with a reduction in the number of acidic sites. This decrease may be attributed to restricted accessibility of the probe molecule (pyridine) to Brønsted sites due to micropore blockage in *BEA. These results demonstrate that the adopted synthesis method effectively produced α-Fe₂O₃/BEA catalysts, with no other crystalline phases of iron(III) oxide detected. Full article