Search Results (77)

In this study, four types of Fe₃O₄-based magnetic nanospheres were functionalized with distinct surface groups to examine how surface chemistry influences their co-transport with tetracycline (TC) in porous media. The functional groups investigated are carboxyl (−COOH), epoxy (−EPOXY), silanol (−SiOH), and amino (−NH₂). Particles bearing −COOH, −EPOXY, or −SiOH are negatively charged, facilitating their transport through porous media, whereas −NH₂-modified particles acquire a positive charge, leading to strong electrostatic attraction to the negatively charged TC and quartz sand, and consequently substantial retention with reduced mobility. Adsorption of TC onto Fe₃O₄-MNPs is predominantly chemisorptive, driven by ligand exchange and the formation of coordination complexes between the ionizable carboxyl and amino groups of TC and the surface hydroxyls of Fe₃O₄-MNPs. Additional contributions arise from electrostatic interactions, hydrogen bonding, hydrophobic effects, and cation–π interactions. Moreover, the carboxylate moiety of TC can coordinate to surface Fe centers via its oxygen atoms. Molecular dynamics simulations reveal a hierarchy of adsorption energies for TC on the differently modified surfaces: Fe₃O₄-NH₂ > Fe₃O₄-EPOXY > Fe₃O₄-COOH > Fe₃O₄-SiOH, consistent with experimental findings. The results underscore that tailoring the surface properties of engineered nanoparticles substantially modulates their environmental fate and interactions, offering insights into the potential ecological risks associated with these nanomaterials. Full article

Current Pt-based methane combustion catalysts require high noble metal loadings (≥1 wt%) and exhibit insufficient low-temperature activity. To address this, we developed a 0.5 wt% Pt catalyst supported by sulfate-modified Fe-Ce-TiO₂ (denoted 0.5Pt/CFT-TS) via sol–gel synthesis using titanium oxysulfate (TiOSO₄) precursor. Control catalysts prepared with TiCl₄, titanium butoxide, or commercial TiO₂ showed inferior performance. Structural characterization revealed that the TiOSO₄ derived carrier possesses a mesoporous framework (156.2 m²/g surface area, 8.1 nm pore size) with residual SO₄²⁻ inducing strong Brønsted acidity (1.23 mmol/g NH₃ adsorption) and elevated Ce³⁺ concentration (49.45%). These properties synergistically enhanced oxygen vacancy density (51.16% O_α fraction) and stabilized sub-nm Pt nanoparticles. The resulting Pt⁰-Fe³⁺/Ce⁴⁺-Oᵥ interface facilitated dynamic redox cycling (Fe³⁺ + Ce⁴⁺ + 0.5O²⁻ ⇌ Fe²⁺ + Ce³⁺ + 0.5Oᵥ + 0.25O₂), lowering oxygen vacancy regeneration barriers (H₂-TPR peak reduced by 45 °C) and decreasing methane activation energy to 46.77 kJ/mol. This catalyst achieved T₉₀ = 163 °C and complete conversion at 450 °C under industrial conditions (1% CH₄/4% O₂, GHSV = 30,000 h⁻¹), establishing a novel design strategy for low-Pt combustion catalysts. Full article

Designing efficient nanoparticle-enhanced CO₂ capture systems is challenging due to the diversity of nanoparticles, solvent formulations, reactor configurations, and operating conditions. This study presents the first ANN-based meta-analysis framework developed to predict CO₂ absorption enhancement across multiple reactor systems, including batch reactors, packed columns, and membrane contactors. A curated dataset of 312 experimental data points was compiled from literature, and an artificial neural network (ANN) model was trained using six input variables: nanoparticle type, concentration, system configuration, base fluid, pressure, and temperature. The proposed model achieved high predictive accuracy (R² > 0.92; RMSE: 4.2%; MAE: 3.1%) and successfully captured complex nonlinear interactions. Feature importance analysis revealed nanoparticle concentration (28.3%) and system configuration (22.1%) as the most influential factors, with functionalized nanoparticles such as Fe₃O₄@SiO₂-NH₂ showing superior performance. The model further predicted up to 130% enhancement for ZnO in optimized membrane contactors. This AI-driven tool provides quantitative insights and a scalable decision-support framework for designing advanced nanoparticle–solvent systems, reducing experimental workload, and accelerating the development of sustainable CO₂ capture technologies. Full article

The solid-state reactions between Fe₂O₃ and molecular sulfur sources could produce FeS nanoparticles efficiently, while the functions of these molecules have been ignored except for the role as sulfur sources. In this work, thioacetamide and thiourea were employed as sulfur sources for the solid-state reactions with Fe₂O₃ to explore their effects on the microstructure and electrochemical performance of the produced FeS. Despite the slight difference in one functional group for two molecules (−CH₃ against −NH₂), thiourea leads to a more complex reaction pathway with FeS₂ as the intermediate phase, while no such an intermediate phase is observed in the reaction with thioacetamide. The former yields FeS of 2D nanoflakes as the final products, compared with the aggregated nanoparticles in reactions with thiourea. As a result, the nanoflakes exhibit a higher discharge capacity with enhanced stability (388.9 mAh∙g⁻¹ vs. 374.7 mAh∙g⁻¹ above 1 V). According to the reaction pathways, the formation of FeS nanoflakes and superior electrochemical performance were addressed, paving a route for the solid-state reactions with molecules to develop high-performance sulfide electrode materials. Full article

Nanotechnology plays an increasingly important role in the economy and human life, which means that more and more amounts of nanosubstances, including nanoparticles of metal oxides, together with wastewater, end up in the environment. This study aimed to study the impact of iron(III) oxide nanoparticles (n-Fe₂O₃), which have magnetic properties, on the efficiency of the Anammox wastewater treatment process. The results indicate that n-Fe₂O₃ in the range of low concentrations may have a positive effect on nitrogen metabolism, increasing the efficiency of NH₄-N removal to 98% in 120 min and at 30 °C. During the first 30 min of the process, when almost anaerobic conditions arose, nanoparticles of Fe₂O₃, stabilized the system by producing ROS. However, a constant control of TOC and pH is necessary because of the constant increase in the amount of organic compounds and H⁺ ions during the reaction. However, a longer contact of n-Fe₂O₃ with biomass causes the efficiency to decrease, and, as a result, the efficiency is lower compared to the system containing only Anammox. Full article

In this study, we report the synthesis and characterization of a novel NH₂-MIL-101(Fe) magnetic composite, developed via in situ formation of NH₂-MIL-101(Fe) in the presence of Fe₃O₄ nanoparticles embedded within a chloropropyl-modified mesoporous silica layer. This hybrid composite retains the high adsorption capacity of NH₂-MIL-101(Fe) while benefiting from the easy magnetic separation enabled by Fe₃O₄ nanoparticles. The mesoporous silica forms a protective porous coating around the magnetic nanoparticles, significantly enhancing its chemical stability and preventing clumping. Beyond protection, the mesoporous silica layer provides a high-surface-area scaffold that promotes the uniform in situ growth of NH₂-MIL-101(Fe). Functionalization of the silica surface with chloride groups enables strong electrostatic interactions between the magnetic component and metal organic framework (MOF), ensuring a homogeneous and stable hybrid structure. The new composite’s capacity to remove Pb(II) and Cd(II) ions from aqueous solutions was systematically investigated. The adsorption data showed a good fit with the Langmuir isotherm model for both ions, the maximum adsorption capacities calculated being 214.6 mg g⁻¹ for Pb(II) and 181.6 mg g⁻¹ Cd(II). Furthermore, the kinetic behavior of the adsorption process was accurately described by the pseudo-second-order model. These findings confirm the effectiveness of this composite for the removal of Pb(II) and Cd(II) ions from aqueous solutions, demonstrating its potential as an efficient material for environmental remediation. The combination of magnetic recovery, high adsorption capacity, and stability makes this novel composite a promising candidate for heavy metal removal applications in water treatment processes. Full article

The removal of heavy metals from industrial wastewater remains a major environmental challenge, demanding efficient, sustainable solutions. This study explores the combined use of Chlorella vulgaris and amine-functionalized magnesium ferrite (MgFe₂O₄-NH₂) nanoparticles to remove cobalt ions from battery effluents. The research aims to explore the capacity of C. vulgaris to adsorb heavy metals, followed by their separation using magnetic nanoparticles. Cobalt adsorption by C. vulgaris was facilitated through the interaction of metal ions on the cell wall, achieving a removal efficiency of 96.44% within 30 min, which increased to 98.78% over 10 h. Amine-functionalized MgFe₂O₄ nanoparticles, synthesized and characterized using HRTEM, FTIR, and VSM, displayed high surface reactivity due to the presence of -NH₂ and -OH groups. At neutral pH, zeta potential measurements revealed a slightly negative charge (−5.6 ± 4.3 mV), while protonation at lower pH levels enhanced electrostatic interactions with the negatively charged algal biomass. Magnetic separation of the cobalt-adsorbed biomass achieved efficiencies ranging from 94.9% to 99.2% within 60 s, significantly outperforming conventional sedimentation methods. SEM and FTIR analyses confirmed the binding of nanoparticles to algal cell walls. The even distribution of MgFe₂O₄ nanoparticles on algal surfaces was further validated by TEM imaging, and the strong magnetic properties of the nanoparticles enabled rapid and efficient separation under an external magnetic field. Full article

In both fundamental and applied scientific exploration, nanostructured protective materials have garnered substantial interest owing to their multifaceted utilization in the fields of medicine, pharmaceuticals, and electronics, among others. This study investigated the evolution of cutting-edge materials for electromagnetic radiation attenuation, with a specific emphasis on the incorporation of superparamagnetic magnetite nanoparticles, Fe₃O₄, into composite systems. The nanoparticles were generated through chemical condensation, meticulously adjusting the proportions of iron salts, specifically FeSO₄·7H₂O and FeCl₃·6H₂O, in conjunction with a 25% aqueous solution of ammonia, NH₄OH·H₂O. This study examined the intricate details of the crystalline structure, the precise composition of phases, and the intricate physicochemical attributes of these synthesized Fe₃O₄ nanoparticles. The analysis was conducted employing a suite of advanced techniques, including scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), and energy-dispersive analysis (EDAX). The key findings of this research suggest that the magnetic nanoparticles generated through chemical condensation have an average size between 10 and 11 nm. This size was determined using BET surface area measurements, which were precise to within 0.1 nm. Moreover, this study demonstrated that incorporating superparamagnetic nanoparticles into composite materials significantly reduces microwave radiation. In particular, an optimal concentration of 0.25% by weight leads to a maximum decrease of 21.7 dB in cement specimens measuring 10 mm in thickness. Moreover, a critical threshold concentration of 0.5 weight percent is established, beyond which the interactions of nanoparticles inhibit the process of remagnetization. These investigations demonstrate that it is feasible to pursue a route towards the development of highly effective electromagnetic shielding materials tailored to specific requirements for diverse applications. Full article

The study focuses on the synthesis of Fe₃O₄@SiO₂-NH₂-Au heterostructures with magneto-plasmonic properties composed of well-defined cubic Fe₃O₄ cores (79 nm) covered with 10 nm silica shell and gold nanoparticles (8 nm) fabricated on silica shell. The surface-anchored MHDA (16-mercaptohexadecanoic acid) linker facilitated cellulase bioconjugation, which was confirmed through Raman spectroscopy. The presence of gold nanoparticle islands on the heterostructure enabled surface-enhanced Raman scattering (SERS), demonstrating the potential for bioactive substance identification. Immobilization of cellulase allowed for pH enhancement and enzyme thermal stability. The optimal pH shifted from 4.0 (free enzyme) to 6.0 while thermal stability increased by 20 °C. The immobilized cellulase kept its 49% activity after five hydrolysis cycles, compared to significantly lower activity for free cellulase. The proposed heterostructures for cellulase immobilization demonstrate potential for practical applications. Full article

Ammonia is one of the common inorganic pollutants in surface waters. It can come from a wide range of sources through the discharge of wastewater (industry, agriculture, and municipal waters). Catalytic ozonation reaction can efficiently remove ammonia nitrogen without introducing other pollutants and improve the nitrogen selectivity of reaction products by controlling the reaction conditions. Catalysts based on silver nanoparticles (Ag NPs) have shown excellent O₃ decomposition performance; therefore, they are promising catalysts for catalytic ammonia ozonation due to their high reactivity, stability, and selectivity to N₂. In this study, we synthesized well-defined silver nanoparticles (Ag NPs) using a modified alkaline polyol method and then dispersed them on solid oxide supports (Fe₃O₄, TiO₂, and WO₃). Before being deposited on the oxide support, the silver nanoparticles were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), and UV-VIS spectroscopy. The obtained catalysts, Ag_Fe₃O₄, Ag_TiO₂, and Ag_WO₃ were characterized using X-ray diffraction (XRD), scanning electron microscopy (SEM), BET surface area analysis, UV-VIS spectroscopy, temperature-programmed reduction (H₂-TPR), and temperature-programmed desorption (TPD) of CO₂ and NH₃. It has been demonstrated that the nature of the support significantly influences the physicochemical properties of the catalysts, as well as their catalytic performance in ammonia ozonation reaction. Full article

Spin crossover (SCO) iron (II) coordination compounds in the form of nanohybrid SCO@SiO₂ particles were prepared using a reverse micelles technique based on the TritonX-100/cyclohexane/water ternary system. Tetraethyl orthosilicate (TEOS) acts as precursor of both the SiF₆²⁻ counter-anion and SiO₂ to obtain Fe(NH₂trz)₃(BF₄)_2−x(SiF₆)_x/2@SiO₂ nanoparticles with different sizes and morphologies while modifying the TEOS concentration and reaction time. The adjustable mixed-anion strategy leads to a range of quite scarce abrupt spin crossover behaviors with hysteresis just above room temperature (ca. 293 K), which is very promising for the integration of these materials into functional devices. Full article

The present work proposes a method for the synthesis of a nanoparticle with a superparamagnetic Fe₃O₄ core coated with SiO₂-NH₂ by ultrasound-assisted coprecipitation. Additionally, the nanoparticle is functionalized with a microinflammation biomarker peptide, and its effects on the viability of monkey kidney endothelial cells and the Vero cell line were evaluated. The main physicochemical properties of the nanoparticles were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), a vibrating sample magnetometer (VSM), a field emission scanning electron, Scanning Electron Microscopy (SEM), and High-Resolution Transmission Electron Microscopy (HR-TEM). The results showed that the nanoparticles are spherical, with sizes smaller than 10 nm, with high thermal stability and superparamagnetic properties. They also demonstrated cell viability rates exceeding 85% through Magnetic Resonance Imaging (MRI). The results indicate the potential of these nanoparticles to be used as a contrast agent in magnetic resonance to detect mild brain lesions. Full article

This study focuses on the development of new amino-functionalized magnetic Fe₂O₃/SiO₂ nanocomposites with varying silicate shell ratios (1:0.5, 1:1, and 1:2) for the efficient elimination of Hg²⁺ ions found in solutions. The Fe₂O₃/SiO₂–NH₂ adsorbents were characterized for their structural, surface, and magnetic properties using various techniques, including Fourier transform infrared spectrum (FT-IR), powder X-ray diffraction (XRD), scanning electron microscopy (SEM), Braunauer–Emmett–Teller (BET), thermogravimetric analysis (TGA), zeta-potential, and particle size measurement. We investigated the adsorption circumstances, such as pH, dosage of the adsorbent, and duration of adsorption. The pH value that yielded the best results was determined to be 5.0. The Fe₂O₃/SiO₂–NH₂ adsorbent with a silicate ratio of (1:2) exhibited the largest amount of adsorption capacity of 152.03 mg g⁻¹. This can be attributed to its significantly large specific surface area of 100.1 m² g⁻¹, which surpasses that of other adsorbents. The adsorbent with amino functionalization demonstrated a strong affinity for Hg²⁺ ions due to the chemical interactions between the metal ions and the amino groups on the surface. The analysis of adsorption kinetics demonstrated that the adsorption outcomes adhere to the pseudo-second-order kinetic model. The study of adsorption isotherms revealed that the adsorption followed the Langmuir model, indicating that the adsorption of Hg²⁺ ions with the adsorbent occurred as a monomolecular layer adsorption process. Furthermore, the thermodynamic analyses revealed that the adsorption of Hg²⁺ ions using the adsorbent was characterized by a spontaneous and endothermic process. Additionally, the adsorbent has the ability to selectively extract mercury ions from a complex mixture of ions. The Fe₂O₃/SiO₂–NH₂ nanocomposite, which is loaded with metal, can be easily recovered from a water solution due to its magnetic properties. Moreover, it can be regenerated effortlessly through acid treatment. This study highlights the potential use of amino-functionalized Fe₂O₃/SiO₂ magnetic nanoparticles as a highly efficient, reusable adsorbent for the removal of mercury ions from contaminated wastewater. Full article

The extensive release of carbon dioxide (CO₂) into the atmosphere is associated with the detrimental impacts of the global environmental crisis. Consequently, the valorization of CO₂ from industrial processes holds great significance. Transforming CO₂ into high added-value products (e.g., CH₄, C₁-C₃ deoxygenated products) has attracted considerable attention. This is feasible through the reverse water–gas shift (RWGS) and Fischer–Tropsch synthesis (FTS) reactions; CO is initially formed and then hydrogenated, resulting in the production of hydrocarbons. Iron-based materials have a remarkable ability to catalyze both RWGS and FTS reactions, enhancing the olefinic nature of the resulting products. Within this context, iron-based nanoparticles, unsupported and supported on zeolite, were synthesized and physico-chemically evaluated, applying multiple techniques (e.g., BET, XRD, FT-IR, Raman, SEM/TEM, DLS, NH₃-TPD, CO₂-TPD). Preliminary experiments show the potential for the production of C₂₊ deoxygenated products. Among the tested samples, supported Fe₃O₄ and Na-Fe₃O₄ (A) nanoparticles on HZSM-5 are the most promising for promoting CO₂ valorization into products with more than two carbon atoms. Results demonstrate that product distribution is highly affected by the presence of acid sites, as low-medium acid sites and medium acidity values enable the formation of C₂₊ hydrocarbons. Full article

The excessive application of nitrogen in tea plantations leads to severe soil acidification and N₂O emission boosting. To promote sustainable agriculture, nanoparticles (NPs) have emerged as alternative fertilizers, but their effects on soil nitrification and greenhouse gas emissions in tea plantations remain unclear. In this study, the effects of NP type (ZnO-NPs and Fe₂O₃-NPs) and dose (0, 1, 10, and 100 mg·kg⁻¹) on soil N₂O emissions were investigated via a lab incubation trial. Soil pH, ammonium, and nitrate changes were also monitored during the incubation period. The abundance of functional genes related to nitrification and denitrification processes was analyzed as well. The results showed that ZnO-NPs led to a decrease in N₂O emissions. The reduction effect was stronger with increasing dose and resulted in a 33% reduction at an addition rate of 100 mg·kg⁻¹. The cumulative N₂O emissions had significantly positive correlations with NH₄⁺-N and NO₃⁻-N. ZnO-NP addition showed a significantly negative effect on Ammonia-Oxidizing Archaea (AOA) but a positive effect on Ammonia-Oxidizing Bacteria (AOB) gene abundance. In contrast, Fe₂O₃-NPs showed an insignificant impact on N₂O emissions and soil N content, as well as nitrification–denitrification gene abundance, regardless of different doses. These results imply that the application of ZnO-NPs may inhibit nitrification through the retarding of AOA activity. This study provided us with a potential practice to reduce N₂O emissions in tea plantations by applying ZnO-NPs, but the efficiency of this reduction needs further examination under ambient conditions before field application. Full article