Search Results (10,798)

Salmonella enteritidis (SE) is recognized as a primary etiological agent of foodborne infection and food poisoning. Selective and sensitive determination of SE in animal-derived products is of great importance for ensuring safety in the food industry. Here, we report a highly sensitive and specific competition assay for detecting SE in eggs without interference from background fluorescence, by using persistent luminescent nanoparticles (PLNPs) as luminescent probes in combination with aptamer recognition and magnetic separation. Initially, the SE-specific aptamer (SEapt), as previously reported, was conjugated onto the surface of Fe₃O₄ magnetic nanoparticles to serve as both the recognition and separation unit. Meanwhile, the ZnGa₂O₄:Cr (PLNPs) were functionalized with the aptamer-complementary DNA (cDNA), serving as the PL signal generator. The constructed PL aptasensor is composed of the aptamer-conjugated MNPs (MNPs-SEapt) and cDNA-functionalized PLNPs (PLNPs-cDNA), integrating the merits of the long-lasting luminescence of PLNPs, the magnetic separation ability of MNPs and the selectivity of the aptamer. This integration offers a promising approach for autofluorescence-free determination of SE in food samples. The proposed aptasensor exhibited excellent linearity in the range from 1.0 × 10²–1.0 × 10⁷ CFU mL⁻¹ with a limit of detection as low as 32 CFU mL⁻¹. The precision for 11 replicate determinations of 1.0 × 10³ CFU mL⁻¹ SE was 3.4% (relative standard deviation). The developed aptasensor achieved recoveries ranging from 98.8% to 102.8% for the determination of SE in the presence of common foodborne bacterial interferents. The method was successfully applied to the analysis of Salmonella genus in egg samples. In principle, the proposed platform may be adapted to other food matrices by substituting the target-specific aptamer, pending target-dependent optimization and validation. Full article

The Mahuaping deposit is the largest Be-W-F deposit in the Jinshajiang–Ailaoshan metallogenic belt, Sanjiang region, SW China, with more than 72,700 t WO₃, 41700 t BeO and 2.3 Mt CaF₂. Despite recent studies, the ore-forming process of the Mahuaping deposit remains poorly understood, limiting further insight into its genesis. In this study, a new muscovite Rb-Sr age and elemental compositions of beryl have been reported to constrain the mineralization age and evolution of ore-forming fluids. Muscovite Rb-Sr isochron dating reveals the mineralization age of the Mahuaping Be-W-F deposit is 28.0 ± 1.5 Ma, indicating the formation of the Mahuaping deposit is probably related to the magmatism caused by the sinistral shearing of crust in the Oligocene. LA-ICP-MS elemental mapping and spot analysis suggest the mechanisms for the incorporation of trace elements into the beryl lattice primarily involve two substitution types: Be²⁺ ↔ Li⁺ + Na⁺/Cs⁺ in the crystal core, and Al³⁺ ↔ (Fe²⁺/Mg²⁺) + (Na⁺/Cs⁺/Rb⁺) occurring in both the core and rim. The enrichment of Fe²⁺ is responsible for the blue coloration observed in beryl. The compositional variation from core to rim in beryl crystal indicates the initial ore-forming fluid of the Mahuaping deposit is reducing and acidic, and dominantly originated from magmatic fluids derived from the highly evolved magma. During the evolution, in addition to the continuous mixing of meteoric water, due to pulsating exsolution, the magmatic fluids were also replenished into the ore-forming fluid, enhancing water/rock interaction. Full article

Wollastonite-1A from Băița Bihor occurs in distal calcic skarns developed in the contact zone of a mainly granodioritic batholith, of Upper Cretaceous age, with Mesozoic limestones and dolostones. Wollastonite generally occurs in the inner part of metasomatic columns, in monomineralic skarns or associated with grossular and molybdenite-2H as ore mineral. The physical properties (i.e., refraction indices α = 1.616, β = 1.629, and γ = 1.631, 2V_α = 39° and density D_m = 2.922(3) g/cm³) are typical for a term close to the stoichiometry, which is confirmed by the chemical analysis. The chemical structural formula of the analyzed wollastonite-1A is (Ca_1.000Mg_0.002Mn_0.001Fe_0.001)(Al_0.004Ti_0.001Si_0.994)O₃, which closely approximates the ideal CaSiO₃. The Gladstone–Dale compatibility indices account for an excellent agreement between physical and chemical data. The mineral can be satisfactorily refined as triclinic, space group $P\overline{1}$, with R₁ = 0.0678 and cell parameters a = 7.9233(3) Å, b = 7.3203(3) Å, c = 7.0651(3) Å, α = 90.053(3)°, β = 95.208(3)°, γ = 103.384(3)°. Both the IR and Raman spectra principally reveal bands related to vibrations of bridged and non-bridged oxygens pertaining to SiO₄ structural tetrahedra. At Băița Bihor, wollastonite-1A is part of the prograde paragenesis, marked by a peak temperature of 550–600 °C. Full article

The dose–response relationship for fluoride (F⁻) exposure remains largely unexplored. Hence, the current study assessed the hepatotoxic and nephrotoxic effects of subacute exposure (28 days) to increasing F⁻ concentrations in Wistar rats via the benchmark dose (BMD5) method. Thirty male rats were assigned to six groups (n = 5): a control group (tap water) along with five groups that received F⁻ via drinking water at increasing concentrations (10, 25, 50, 100, and 150 mg/L). F⁻ toxicity was determined via water intake, weight gain, histological analyses, redox status, and essential element levels. PROASTweb 70.1 software was utilized to investigate the external and internal F⁻ dose–response relationships. Specified major cytoarchitecture damage and superoxide anion (O₂·⁻), total oxidative status (TOS), superoxide dismutase (SOD) activity, total thiol groups (SH), and advanced oxidation protein product (AOPP) level alterations were detected in both sets of tissues. Moreover, F⁻ caused an imbalance in copper (Cu), zinc (Zn), iron (Fe), and manganese (Mn). The most sensitive parameters were O₂·⁻ (0.06 mg F⁻/kg) in the liver and AOPP (6.5 × 10⁻⁶ mg F⁻/L) in the kidneys. These findings contribute to the limited risk assessment of fluorides and highlight the dose-dependent relationship between redox status parameters and bioelements in the liver and kidneys. Full article

Repairing maxillofacial bone defects remains a major clinical challenge due to inadequate vascularisation and poor integration with host tissue. While bioactive scaffolds have shown promise in supporting osteogenesis and angiogenesis, achieving robust and synchronised dual regenerative outcomes is still elusive. This study presents a multifunctional, cell-free magnetic hydrogel platform designed to biomimetically coordinate osteogenic and angiogenic processes for effective maxillofacial bone regeneration. The composite poly(vinyl alcohol)-vaterite (PVA-Vat) hydrogel scaffold incorporates tuneable magnetic nanoparticles (MNPs) composed of single-domain superparamagnetic iron oxide (Fe₃O₄). By harnessing magneto-mechanical cues to orchestrate bilateral communication between human bone mesenchymal stem cells and endothelial cells, this platform provides a deeper mechanistic understanding of coupled tissue regeneration and delivers superior dual-regenerative performance for maxillofacial bone repair. Under magnetic stimulation, a coculture system demonstrated strong osteogenesis-angiogenesis coupling mediated by reciprocal VEGFA-BMP2 signalling. This reciprocal crosstalk was evidenced by a synergistic amplification of VEGFA and BMP2 expression in coculture compared to monocultures, where MNP-stimulated osteoprogenitors secreted VEGFA to drive endothelial capillary-like network formation, while endothelial cells reciprocally enhanced endogenous BMP2 levels to accelerate osteoblastic mineralisation. These findings establish MNP-integrated hydrogels as a cell-free, multifunctional platform capable of synchronising dual regenerative pathways, offering a biomimetic strategy to overcome vascularisation and integration barriers in maxillofacial bone repair. Full article

Owing to the high stability and low cost of nanozymes, they have been extensively investigated and reported. In this work, highly active CeO₂ nanoflowers were first prepared and then different metal elements were doped into the CeO₂ nanoflower matrix via a novel synthesis method to fabricate M-CeO₂ (M = Cu, Fe, Co, Mn, La) nanomaterials. Mn-CeO₂ with the highest peroxidase-like activity was selected via systematic screening, the as-prepared Mn-CeO₂ nanocomposites exhibited enhanced enzyme-like activity due to the strong metal-support interaction. This article explored the effects of doping ratio, pH, temperature, reaction time, and material concentration on its activity. A simple sensitive and selective colorimetric method was established and successfully used to detect hydrogen peroxide and ascorbic acid sensitively. When the hydrogen peroxide (H₂O₂) concentration is within the 2.0–120.0 μM range, the UV-visible absorbance at 652 nm was associated linearly with the H₂O₂ concentration, R² = 0.9959, LOD = 1.7 μM (S/N = 3). The absorbance of the reaction system showed a good linear relationship with the ascorbic acid (AA) concentration (1.0–40.0 μM, R² = 0.992), LOD = 0.98 μM (S/N = 3). This study provides an effective way to construct efficient nanozymes and their potential applications in sensing and detection. Full article

Birefringence, arising from the low-symmetry structure in orthorhombic LaFeO₃, limits the observation and utilization of magneto-optical effects. In this study, the pure-phase perovskite-typed La_1−xCe_xFe_1−xTi_xO₃/SiO₂ thin films were successfully fabricated via radio-frequency magnetron sputtering, where the co-doping of Ce³⁺ and Ti⁴⁺ ions effectively induced a structure transition from orthorhombic to a highly symmetric cubic phase, eliminating birefringence effect and thus reducing optical transmission loss. At the same time, the doped Ce³⁺ ions also effectively enhanced the magnetic and magneto-optical effects of the system due to their strong spin coupling effect and superexchange interaction with Fe³⁺ ions. The results show that the cubic-phase La_0.5Ce_0.5Fe_0.5Ti_0.5O₃/SiO₂ thin film exhibits excellent magnetic and magneto-optical performance. Their saturation magnetization reaches 180 emu/cm³ with an in-plane easy magnetic axis. And their magnetic circular dichroic ellipticity |ψ_F| reaches 3054 degrees/cm. Full article

Both Co-free and lithium- and manganese-rich layered oxide Li(Li_0.2Mn_xNi_yFe_z)O₂ (MNF) cathodes have recently attracted attention in lithium-ion battery (LIB) research due to their high capacities of over 250 mAhg⁻¹, as well as being more eco-friendly and inexpensive than commercial NMC and LiCoO₂. However, they still suffer from lower experimental capacity as well as capacity decay, voltage fade, poor rate capability, and thermal instability. In this paper, fluorine (F)-doped Li_1.2(Mn_0.5Ni_0.2Fe_0.1)O_2(1−x)F_2x (MNF502010, x = 0, 0.025, 0.05, 0.075, 0.1) cathode materials have been synthesized in the nanoscale via sol–gel and subsequent solid-phase calcination to address some of these problems. The resulting 5% F-doped MNF502010 cathode demonstrates the advantage of fluorine doping, which makes a significant contribution to the formation of a well-ordered layer structure with a minimal LiM₂O₄ spinel phase as an impurity. This composition achieves an initial discharge capacity of 252 mAhg⁻¹ (1C = 250 mAhg⁻¹) and a 156 mAhg⁻¹ discharge capacity at 0.3 C on the 100th discharge, with an average voltage fade of 0.24 V. The optimization of fluorine composition results in an enhancement in the activation of the Li₂MnO₃-type monoclinic phase, as well as an increase in the electronic conductivity compared to the fluorine-free cathode. To understand the structural origin of this improved performance, X-ray absorption spectroscopy (XAS) measurements were carried out on pristine and cycled MNF electrodes. Full article

One of the significant causes of failure in aerospace engine components is high-temperature oxidation. Therefore, it is necessary to investigate the high-temperature oxidation behavior of newly fabricated structural materials for aerospace components. From this perspective, the isothermal oxidation behavior and kinetics of newly developed stainless steel (SS) 08X14H were investigated at 750, 950 and 1050 °C for up to 100 h in an air environment. The weight results demonstrate that oxidation in 08X14H increases with time and temperature and follows a parabolic rate law. Major spallation was observed in samples oxidized for 100 and 24 h at 950 °C and 1050 °C, respectively. Structural and morphological analysis of oxidized samples through X-ray diffraction (XRD) and field emission scanning electron microscopy (FESEM) of the surface and cross section reveal the phases present and their distribution. The structural results confirm the formation of Fe₂O₃, Cr₂O₃, FeCr₂O₄ and intermediate (Cr, Fe)₂O₃ oxides in the oxidized samples. Surface morphologies reveal that the formation of a Cr₂O₃ layer effectively protects the material from further oxidation. At higher temperatures, the coarsening of Fe₂O₃ oxides takes place, which leads to the formation of loose and porous oxide scale with stress-induced cracks. The spallation of the outermost Fe₂O₃-rich oxide scale was observed, and the matrix is exposed during the extreme oxidation at 950 and 1050 °C for 100 and 50 h, respectively. The cross-sectional morphologies and elemental mapping results reveal a duplex oxide layer with an outermost Fe₂O₃ layer followed by an underlying layer of Cr₂O₃, (Cr, Fe)₂O₃ and FeCr₂O₄ spinel beneath the Fe₂O₃ layer. Full article

CaFe₂O₄ is a p-type ferrite semiconductor of interest for photo-assisted environmental remediation due to its narrow band gap and high chemical stability. In this work, CaFe₂O₄ powders were synthesized via the Pechini polymeric precursor method and calcined between 550 and 850 °C to investigate the influence of calcination temperature on structural order and material properties. X-ray diffraction combined with Rietveld refinement revealed the progressive stabilization of the orthorhombic Pnma phase, accompanied by relaxation of the FeO₆ octahedral framework. Raman and FT-IR spectroscopies confirmed a significant increase in vibrational coherence with increasing calcination temperature, quantified by a nearly three-fold increase in the global Raman order parameter and phonon lifetimes. Nitrogen physisorption showed a modest specific surface area and a pore system dominated by interparticle meso–macroporosity, typical of thermally treated ferrites. Removal tests using ciprofloxacin under UV-A irradiation showed limited photo-assisted activity, while agar diffusion assays against Escherichia coli and Staphylococcus aureus revealed no inhibition halos, indicating the absence of detectable antibacterial activity under the experimental conditions employed. Overall, CaFe₂O₄ combines photo-assisted response with good structural stability, highlighting its potential as a chemically stable ceramic material with no detectable antibacterial activity under the tested conditions. Full article

The present study investigates the morphology, chemical composition, and phase constitution of oxide scales formed on the Fe40Al5Cr0.2TiB intermetallic alloy after long-term oxidation at 700 °C for 2000 h in air and water vapor environments. The results demonstrate the formation of an extremely thin oxide scale (≈300 nm), composed predominantly of α-Al₂O₃, which provides effective protection against further oxidation. The oxide layer exhibits locally heterogeneous morphology, including whisker-like structures and fine crystallites. Due to the very limited thickness of the oxide scale, significant challenges arise in the interpretation of microanalytical data. It is shown that the accelerating voltage strongly influences the effective information depth in SEM-EDS analysis, leading to a substantial contribution from the substrate even at low voltages. Monte Carlo simulations were used to support the interpretation of electron–matter interactions and to explain the observed discrepancies in chemical analysis. The study demonstrates that reliable characterization of ultrathin oxide scales requires careful optimization of SEM parameters and the combined use of complementary techniques, including EDS/WDS, XRD, and EBSD. The findings highlight the importance of methodological considerations in the analysis of thin oxide layers and provide guidance for the correct interpretation of experimental data in similar systems. Full article

CoFe₂O₄ nanoparticles were prepared using a hydrothermal method. All the studied samples were single-phase and were crystallized in a cubic Fd-3m structure. XRD and TEM analyses revealed that the particles had average sizes between 5 and 22 nm. It has been shown that, by using the PVP of different molecular masses, trends of growth and crystallization can be established, obtaining elongated 40 k, cubical 58 k, and rhomboidal 360 kg/mol nanoparticles. While using Ethylene glycol as solvent, the formation of separated “raspberry”-like nanostructures was revealed. The saturation magnetizations are somewhat smaller compared with crystalline CoFe₂O₄ saturation magnetization, but are high enough to have possible biomedical applications. FC and ZFC measurements show that the blocking temperature was around 100 K for the CF5 sample and around 20 K for the FC6 sample. The calculated anisotropy constants were between 7 and 10 kJ/m³, being close to previously reported values. The calculated blocking temperatures are in good agreement with experimental ones. The M_r/Ms ratio at room temperature was lower than 0.5, confirming the predominance of magnetostatic interactions. This paper serves as a good starting point for researchers seeking to synthesize a CoFe₂O₄ system with a desired size and growth tendency at the nanometer scale. Full article

To detect volatile organic compounds, fabricating gas sensors with high sensitivity, excellent selectivity, low detection limits, and good long-term stability is critical. Herein, Er_1/3Yb_1/3La_1/3FeO₃ medium-entropy material was synthesized via the sol–gel method and characterized in terms of its morphological, structural, and chemical properties. The medium-entropy design induces significant lattice distortion and increased oxygen vacancies, leading to higher adsorbed oxygen content and hole concentration on the material surface, which enhances the activity of gas-sensing reactions. The Er_1/3Yb_1/3La_1/3FeO₃ sensor exhibits a response of 13.2 toward 10 ppm of butanone gas at the optimum operating temperature of 192 °C, which is nearly three times the response of the ErFeO₃ sensor (4.5), along with excellent selectivity to butanone gas, a low detection limit (0.5 ppm), and long-term stability. Moreover, the applied magnetic fields improve the ordering of magnetic moments in both Er_1/3Yb_1/3La_1/3FeO₃ and O₂ molecules, which facilitates gas adsorption and electron transfer, and further boosts the gas-sensing performance. The response of the Er_1/3Yb_1/3La_1/3FeO₃ sensor toward 10 ppm butanone is enhanced to 21.3 under the applied magnetic field of 680 mT, which improves the selectivity toward butanone. This work provides a novel material design strategy for the detection of VOCs and a feasible magnetic field-assisted approach for optimizing the gas-sensing performance of perovskite ferrite materials. Full article

Pesticides are a major cause of water contamination, making this issue a major environmental and public health concern. In this context, the development of advanced and effective remediation materials is needed. In this study, a titanium-functionalized magnetic silica aerogel (AG-Ti@Fe₃O₄-SA) was successfully prepared via microfluidics and evaluated for water decontamination. The structural and compositional features of the aerogel were determined using XRD, FT-IR, RAMAN, SEM, TEM, BET, and DLS, confirming the formation of the aerogel with dispersed Fe₃O₄-SA nanoparticles and the successful incorporation of titanium within the aerogel matrix. Regarding decontamination potential, the aerogel was tested against a pesticide mixture, yielding pesticide-dependent removal efficiencies (16–100%). Notably, the aerogel exhibited a high affinity for organophosphorus pesticides and a moderate affinity for polar compounds, whereas bulky hydrophobic pesticides showed lower adsorption. In vitro, the aerogel induced a moderate decrease in HaCaT cell viability after 48 h of exposure, accompanied by a slight increase in lactate dehydrogenase release, while HEK293 cells remained largely unaffected, indicating a cell-type-dependent biological response. Overall, the findings from this screening-level study recommend AG-Ti@Fe₃O₄-SA aerogel as a promising selective adsorbent for pesticide removal. Full article

Water contamination by synthetic dyes such as malachite green (MG) remains a significant environmental and public health challenge due to their high toxicity, chemical stability, and resistance to biodegradation. In this study, a CaO-CuFe₂O₄ composite was synthesized through a sustainable route using eggshells and orange peel as agro-industrial waste precursors. Comprehensive structural, spectroscopic and microscopic analyses confirmed the coexistence of a predominant CaO-based phase with spinel CuFe₂O₄, together with nanometric features, satisfactory elemental dispersion and practical magnetic recoverability. Under the experimental conditions employed, the composite exhibited high adsorption performance towards MG, reaching an equilibrium capacity of 2288.4 mg g⁻¹ and 99.98% decolorization within 60 min. The kinetics were better described by the pseudo-second-order model, while the equilibrium behavior was more satisfactorily fitted by the Langmuir isotherm than by the Freundlich model. Thermodynamic analysis indicated that the adsorption process was favorable over the temperature range studied and became more pronounced at higher temperature. The results suggest that the adsorption behavior arises from the combined influence of surface chemistry, calcium-derived basic sites, ferrite-associated metal centers and interfacial accessibility, rather than from surface area alone. In addition, the material could be readily separated from aqueous solution using an external magnetic field, highlighting its practical post-treatment recoverability. Overall, this work demonstrates a viable waste valorization strategy for the development of a magnetically recoverable CaO-CuFe₂O₄ adsorbent for cationic dye removal. Beyond the specific case of MG, the study underscores the potential of agro-waste-derived hybrid oxides as application-relevant materials for water remediation. Full article