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A microbial fuel cell (MFC) is a modern, environmentally friendly, and cost-effective energy conversion technology that utilizes renewable organic waste as fuel, converting stored chemical energy into usable bioelectricity in the presence of a biocatalyst. Despite advancements in MFC technology, several challenges remain in optimizing power production efficiency, particularly regarding anode materials and modifications. In this study, low-cost biosynthesized iron oxide nanoparticles (Fe3O4 NPs) were coated with a polyaniline (PANI) conducting matrix to synthesize hybrid Fe3O4/PANI binary nanocomposites (NCs) as modified MFC anodes via an in-situ polymerization process. Characterization techniques, including UV–Vis, XRD, SEM, and FT-IR, revealed the successful synthesis of green-routed nano-scaled materials with altered optical properties after matrix coating, high crystallinity in the iron oxide phase, rougher surface morphology, and characteristic Fe–O peaks at 594 cm⁻1. Additionally, the electrochemical behavior of the prepared nano-materials was characterized by cyclic voltammetry (CV), where low ΔEp values (0.473 V) for Fe3O4/PANI NCs indicated the presence of reversible charge transfer mechanisms at the electrode surface, reflecting a high rate of electron transfer. The synthesized nanocomposite was used to modify pencil graphite anodes to construct four single-chamber MFCs: bare pencil graphite anodes, pencil graphite anodes modified with Fe3O4, PANI, and Fe3O4/PANI nanocomposites. The maximum open circuit voltage (OCV) value was 645 ± 24.50 mV, with a high power output of 424.51 ± 6.86 mW/m2 and current density of 2475.01 ± 1.23 mA m−2 produced by the Fe3O4/PANI NCs modified pencil graphite electrode, which is more than six times the efficiency in terms of power density compared to the unmodified pencil graphite electrode (PGE). These results demonstrate that the synthesized nanocomposite plays an effective and value-added role in modifying traditional carbon anode electrodes within an MFC energy conversion device system. [ABSTRACT FROM AUTHOR]

To further enhance the safety and energy efficiency of the Fe3O4 preparation experiment, we proposed a strategy for synthesizing monodisperse Fe3O4 microspheres through a one-step solvothermal process. In this environmentally friendly synthesis method, stable FeCl3∙6H2O was utilized as the sole raw material, while ethylene glycol, characterized by its high boiling point and favorable safety profile, served as the solvent. Additionally, inexpensive and readily available urea was selected to function either as a mineralizer or surfactant. Through this one-step solvothermal reaction, the target product of Fe3O4 could be obtained without subsequent calcination under reducing or inert atmospheres, thereby enhancing experimental safety and promoting energy conservation. By controlling the amount of urea added, it became feasible to produce monodisperse magnetic Fe3O4 microspheres characterized by complete crystallinity and high yield. Utilizing the as-synthesized Fe3O4 as a catalyst, we investigated its photocatalytic activity against xylenol orange organic dyes along with its regeneration characteristics. When 40 mmol of urea was incorporated into the reaction mixture, the resulting Fe3O4 sample exhibited optimal photocatalytic performance; a 20 mg/L xylenol orange solution became colorless and transparent after just 1.5 h of UV light irradiation. Furthermore, during five consecutive regeneration cycles, its catalytic activity could be restored to its initial level. Importantly, Fe3O4 demonstrated excellent magnetic sensitivity properties that facilitated rapid targeted separation under an external magnetic field, providing convenience for recovery and collection purposes. [ABSTRACT FROM AUTHOR]

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Nanocomposites based on Fe3O4 and carbonaceous nanoparticles (CNPs), including carbon nanotubes (CNTs) and graphene derivatives (graphene oxide (GO) and reduced graphene oxide (RGO)), such as Fe3O4@GO, Fe3O4@RGO, and Fe3O4@CNT, have demonstrated considerable potential in a number of health applications, including tissue regeneration and innovative cancer treatments such as hyperthermia (HT). This is due to their ability to transport drugs and generate localized heat under the influence of an alternating magnetic field on Fe3O4. Despite the promising potential of CNTs and graphene derivatives as drug delivery systems, their use in biological applications is hindered by challenges related to dispersion in physiological media and particle agglomeration. Hence, a solid foundation has been established for the integration of various synthesis techniques for these nanocomposites, with the wet co-precipitation method being the most prevalent. Moreover, the dimensions and morphology of the composite nanoparticles are directly correlated with the value of magnetic saturation, thus influencing the efficiency of the composite in drug delivery and other significant biomedical applications. The current demand for this type of material is related to the loading of a larger quantity of drugs within the hybrid structure of the carrier, with the objective of releasing this amount into the tumor cells. A second demand refers to the biocompatibility of the drug carrier and its capacity to permeate cell membranes, as well as the processes occurring within the drug carriers. The main objective of this paper is to review the synthesis methods used to prepare hybrids based on Fe3O4 and CNPs, such as GO, RGO, and CNTs, and to examinate their role in the formation of hybrid nanoparticles and the correlation between their morphology, the dimensions, and optical/magnetic properties. [ABSTRACT FROM AUTHOR]

Fe3O4 nanoparticles (NPs) with a continuous and mesoporous silica (m-SiO2) shell were synthesized using a one-step method, sourcing silica from rice husk ash (RHA). The rice husk was thermally treated to obtain ash, from which silica was extracted as sodium silicate and precipitated by pH reduction. This silica powder, combined with iron chloride salts, facilitated the synthesis of the core-shell NPs. Mint extract acted as a capping agent to prevent agglomeration, and CTAB (cetyltrimethylammonium bromide) was used to create the porous SiO2 shell. X-ray diffraction (XRD), Field emission scanning electron microscopy (FESEM), and transmission electron microscopy (TEM) characterization investigated the structure, size, and shell formation. Fourier transform infrared spectroscopy (FTIR) and dynamic light scattering (DLS) assessed coating integrity and suspension stability. DLS analysis showed a relatively narrow particle size distribution with an average hydrodynamic size of 72.6 nm. Small-angle X-ray scattering (SAXS) provided insights into the meso- and nanoscale structure, while BET and nitrogen adsorption-desorption isotherms confirmed the mesoporous nature of the silica shell. Magnetization measurements showed superparamagnetic behavior, with specific magnetization values of 57.9 emu/g for Fe3O4 and 27.5 emu/g for Fe3O4@m-SiO2. These results confirm the successful synthesis of superparamagnetic magnetite NPs with a mesoporous silica coating from RHA. [ABSTRACT FROM AUTHOR]

In this research, a modified magnetic nanocomposite based on layered double hydroxide (Fe3O4/C/CoFe-LDH) was synthesized through co-precipitation and thermal processes. Modification of the magnetic nanoparticles was carried out by applying a carbon coating. After the surface modification of these nanoparticles, LDH was immobilized on the surface of Fe3O4/C. To synthesize CoFe-LDH, a co-precipitation process was performed using cobalt (II) nitrate and iron (III) nitrate. The synthesized nanocomposite was characterized by FT-IR, XRD, SEM, EDS, STA, TEM, VSM and BET. After identifying of Fe3O4/C/CoFe-LDH, its catalytic activity in the Hantzsch reaction was evaluated. The investigations exhibited that in the presence of the designed catalyst, the expected products can be produced with a high yield in a very short time. In addition, the recyclability and reusability of the prepared nanocomposite were evaluated. The results of these investigations show that after four cycles, the recycled catalyst still maintains its activity and only causes a slight decrease in the reaction efficiency. [ABSTRACT FROM AUTHOR]

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. [ABSTRACT FROM AUTHOR]

The purpose of this research is to design nanocomposite materials for biomedical applications. New conjugates of PEG derivatives of RGD peptides and magnetic nanoparticles, based on Fe3O4 (MNPs) with silica coating covalently labelled with fluorescent dye Cyanine5, were obtained. It was shown that a higher loading level of RGD peptides occurred in the case of MNPs with SiO2/aminopropylsilane coating, synthesised using N-(phosphonomethyl)iminodiacetic acid (PMIDA) as a surfactant. To confirm the structure and chemical purity of the new RGD-PEG conjugate, a number of methods were used, including 1H NMR, HRMS, and RP-HPLC. The characterisation of MNPs was carried out using the following physical methods: TEM, FTIR, EDX, CHN analysis, DLS, fluorescence spectrometry, vibration magnetometry, and relaxometry. Samples obtained from PMIDA-stabilised MNPs contained a greater amount of the peptide and possessed better hydrodynamic characteristics than samples obtained from non-stabilised MNPs. A comparative study of the MNP cytotoxicity was carried out towards 4T1 and MDA-MB231 cell lines (MTT test), and the possibility of cell labelling was assessed. The cellular uptake was more efficient for nanoconjugates obtained without PMIDA. The data obtained can be used for the design of materials for cell labelling and visualisation. [ABSTRACT FROM AUTHOR]

This study investigates the production of TiO2/Fe3O4/C hydrophilic magnetic nanocomposites produced via a one-step novel method using the submerged arc discharge method applied in liquid media of ethanol and ethanol–ammonia under the influence of external magnetic field. The magnetized submerged arc discharge forms a longer-lasting plasma arc, thereby affecting the growth of spherical and tubular carbon nanocomposites. More reactive species enrolled in the carbon growth in the magnetized submerged arc discharge, resulting in the ordered crystalline structure. The nanocomposites synthesized in ethanol–ammonia show hydrophilic characteristics, indicated by their dispersion improvement in the water and the presence of the vibrations of hydroxyl, amine, and –CN functional groups in Fourier transfer infrared (FTIR) spectra. The preparation technique described in this study using magnetized submerged arc discharge is supposed to be a simple and less costly preparation method that can potentially be further applied to produce numerous other nanocomposites. [ABSTRACT FROM AUTHOR]

MoS2@Fe3O4 composite was fabricated via two-step hydrothermal method, utilizing cetyltrimethyl ammonium bromide(CTAB) as a soft template, thioacetamide as a sulfur source, and sodium molybdate as a molybdenum source. The morphology and structure of MoS2@Fe3O4 were analyzed by SEM and XRD. The efficiency and mechanism of catalytic degradation of iodoprolol(IPM) by MoS2@Fe3O4/H2O2 system was evaluated. The results showed that Fe3O4 was deposited on the surface of MoS2, and MoS2@Fe3O4 had a uniformly dispersed flower ball structure, which provided more catalytic active sites. Under the conditions of initial pH of 4, MoS2@Fe3O4 dosage of 0.15 g/L, H2O2 concentration of 0.5 mmol/L, and IPM concentration of 5 μmol/L, the degradation rate of IPM by MoS2@Fe3O4/H2O2 system reached 89.85% after 30 minutes of reaction. Compared with Fe3O4/H2O2 system, the degradation rate of IPM increased by about 12%. The applied magnetic field facilitated the reusability of MoS2@Fe3O4. The main active species for IPM degradation by the MoS2@Fe3O4/H2O2 system were ·OH and 1O2. The degradation rate of the MoS2@Fe3O4/H2O2 system on IPM remained stable over 80% after 6 cycles, suggesting that MoS2@Fe3O4 had good stability.

Fe3O4 nanoparticles (NPs) with a continuous and mesoporous silica (m-SiO2) shell were synthesized using a one-step method, sourcing silica from rice husk ash (RHA). The rice husk was thermally treated to obtain ash, from which silica was extracted as sodium silicate and precipitated by pH reduction. This silica powder, combined with iron chloride salts, facilitated the synthesis of the core-shell NPs. Mint extract acted as a capping agent to prevent agglomeration, and CTAB (cetyltrimethylammonium bromide) was used to create the porous SiO2 shell. X-ray diffraction (XRD), Field emission scanning electron microscopy (FESEM), and transmission electron microscopy (TEM) characterization investigated the structure, size, and shell formation. Coating integrity and suspension stability were assessed through Fourier transform infrared spectroscopy (FTIR) and dynamic light scattering (DLS). DLS analysis showed a relatively narrow particle size distribution with an average hydrodynamic size of 72.6 nm. Small-angle X-ray scattering (SAXS) provided insights into the meso- and nanoscale structure, while BET and nitrogen adsorption-desorption isotherms confirmed the mesoporous nature of the silica shell. Magnetization measurements showed superparamagnetic behavior, with specific magnetization values of 57.9 emu/g for Fe3O4 and 27.5 emu/g for Fe3O4@m-SiO2. These results confirm the successful synthesis of superparamagnetic magnetite NPs with a mesoporous silica coating from RHA.

Abstract Background The progression of triple-negative breast cancer is shaped by both tumor cells and the surrounding tumor microenvironment (TME). Within the TME, tumor-associated macrophages (TAMs) represent a significant cell population and have emerged as a primary target for cancer therapy. As antigen-presenting cells within the innate immune system, macrophages are pivotal in tumor immunotherapy through their phagocytic functions. Due to the highly dynamic and heterogeneous nature of TAMs, re-polarizing them to the anti-tumor M1 phenotype can amplify anti-tumor effects and help mitigate the immunosuppressive TME. Results In this study, we designed and constructed an ultrasound-responsive targeted nanodrug delivery system to deliver Siglec-G siRNA and Fe3O4, with perfluorohexane (PFH) at the core and mannose modified on the surface (referred to as MPFS@NDs). Siglec-G siRNA blocks the CD24/Siglec-G mediated “don’t eat me” phagocytosis inhibition pathway, activating macrophages, enhancing their phagocytic function, and improving antigen presentation, subsequently triggering anti-tumor immune responses. Fe3O4 repolarizes M2-TAMs to the anti-tumor M1 phenotype. Together, these components synergistically alleviate the immunosuppressive TME, and promote T cell activation, proliferation, and recruitment to tumor tissues, effectively inhibiting the growth of primary tumors and lung metastasis. Conclusion This work suggests that activating macrophages and enhancing phagocytosis to remodel the TME could be an effective strategy for macrophage-based triple-negative breast cancer immunotherapy.

This study investigates the production of TiO2/Fe3O4/C hydrophilic magnetic nanocomposites produced via a one-step novel method using the submerged arc discharge method applied in liquid media of ethanol and ethanol–ammonia under the influence of external magnetic field. The magnetized submerged arc discharge forms a longer-lasting plasma arc, thereby affecting the growth of spherical and tubular carbon nanocomposites. More reactive species enrolled in the carbon growth in the magnetized submerged arc discharge, resulting in the ordered crystalline structure. The nanocomposites synthesized in ethanol–ammonia show hydrophilic characteristics, indicated by their dispersion improvement in the water and the presence of the vibrations of hydroxyl, amine, and –CN functional groups in Fourier transfer infrared (FTIR) spectra. The preparation technique described in this study using magnetized submerged arc discharge is supposed to be a simple and less costly preparation method that can potentially be further applied to produce numerous other nanocomposites.

Effects of Fe-based nanoparticles (Fe2O3 and Fe3O4) on germination parameters were studied for some seedling characteristics of Oriental beech (Fagus orientalis) seeds. Fe2O3 and Fe3O4 nanoparticle applications were made at concentrations of 400, 800, 1200, 1600, and 2000 mg/L on Fagus orientalis seeds collected from 10 different populations, and some germination and seedling characteristics were evaluated. Preliminary results generally indicated that low-dose nanoparticle applications positively affected germination and seedling characteristics, while increases in doses led to decreases in these parameters. Values obtained from high-dose nanoparticle applications were generally lower than those from the control group. The iron nanoparticles affected the parameters to different extents, Fe2O3 nanoparticles showed a significant positive effect on germination rate and radicle length, while exhibiting a significant negative effect on germination percentage and plumule length. The populations least affected by high-dose iron nanoparticle applications were Bursa Inegol, Karabuk-Yenice, and Ordu Akkus, while the most affected were the Bartin-Kumluca and Kahramanmaras-Andirin populations.

Abstract A novel composite material, magnetic chitosan-clay/benzoin/Fe3O4 (CS-CY/Benz/Fe3O4), was synthesized for effectively removing thionine dye (TH) from water solutions. The structural integrity and suitability of CS- CY/Benz/Fe3O4 composite for adsorption purposes were validated through extensive characterization techniques including BET, XRD, FTIR, and SEM. The adsorption efficiency was optimized through a Box–Behnken design (BBD) employing response surface methodology (RSM), focusing on variables such as adsorbent dose (A: 0.02–0.08 g), solution pH (B: 4–10), temperature (C: 30–60 °C), and time (D: 5–30 min). Experimental results revealed a maximum TH removal of 99% with significant interactions between temperature (C) and time (D) (p-value = 0.0001). The optimal conditions for TH removal were determined as pH ~ 5.91, adsorbent dosage of 0.08 g, temperature of 54.34 °C, and time of 29.7 min. The investigation of kinetics revealed that the adsorption process conformed to a pseudo-second-order (PSO) model, while the equilibrium data were effectively described by the Freundlich isotherm model. At a temperature of 333.15 K and a TH concentration of 350 mg/L, the adsorption capacity was determined to be 660.86 mg/g. The mechanism of adsorption encompassed various interactions such as electrostatic attractions, n–π interactions, hydrogen bonding, and Yoshida H-bonding. Particularly, the CS-CY/Benz/Fe3O4 composite demonstrated strong magnetic responsiveness, enabling straightforward separation from water using an external magnetic field after adsorption. Particularly, the CS-CY/Benz/Fe3O4 composite demonstrated strong magnetic responsiveness, enabling straightforward separation from water using an external magnetic field after adsorption. This research contributes important findings to the advancement of magnetic chitosan-based composites for efficient removal of TH dye pollutants from water environments.

Abstract This article is devoted to the synthesis of a new magnetic palladium catalyst that has been immobilized on A-TT-Pd coated-magnetic Fe3O4 nanoparticles. Such surface functionalization of magnetic particles is a promising method to bridge the gap between heterogeneous and homogeneous catalysis approaches. The structure, morphology, and physicochemical properties of the particles were characterized through different analytical techniques, including TEM, FT-IR, XRD, SEM, EDS, TGA-DTG, ICP, and VSM techniques. The obtained Fe3O4@SiO2@A-TT-Pd performance can show excellent catalytic activity for the synthesis of diaryl ethers and oxidation of sulfides, and the corresponding products were obtained with high yields. The advantages of this catalyst include a simple test method, green reaction conditions, no use of dangerous solvents, short reaction time, low catalyst loading, and reusability. Also, the nanocatalyst was easily separated from the reaction mixture with the help of a bar magnet and recovered and reused several times without loss of stability and activity.

High spin polarization and low resistivity of Fe3O4 at room temperature have been an appealing topic in spintronics with various promising applications. High-quality Fe3O4 thin films are a must to achieve the goals. In this report, Fe3O4 films on different substrates (SiO2/Si(100), MgO(100), and MgO/Ta/SiO2/Si(100)) were fabricated at room temperature with radio-frequency (RF) sputtering and annealed at 450 °C for 2 h. The morphological, structural, and magnetic properties of the deposited samples were characterized with atomic force microscopy, X-ray diffractometry, and vibrating sample magnetometry. The polycrystalline Fe3O4 film grown on MgO/Ta/SiO2/Si(100) presented very interesting morphology and structure characteristics. More importantly, changes in grain size and structure due to the effect of the MgO/Ta buffering layers have a strong impact on saturation magnetization and coercivity of Fe3O4 thin films compared to cases of no or just a single buffering layer.

Autoclave corrosion testing has been used for many years; however, few have studied the effect of its shortcomings on the formation of corrosion products and corrosion behaviour. In particular, understanding of these effects under high temperature and high pressure (HTHP) is rare. In this study, we highlighted the important parameters such as heating periods, flow rates and volume-to-surface ratios influencing carbon steel corrosion in the early stages. Especially, characterisation and protection behaviour of corrosion products associated with corrosion behaviour in the heating stage under the geothermal CO2-containing environment were systematically studied via mass loss, in-situ electrochemistry and surface analysis techniques. The roles of pCO2, volume-to-surface ratio and flow rate influence the formation of the corrosion products in the early stage are also evaluated.

Abstract Delivering anticancer drugs to the appropriate site within the body poses a critical challenge in cancer treatment with chemotherapeutic agents like doxorubicin (DOX). Magnetic graphene oxide (GO) nanosheets with generation 1 (G1) amidoamine-dendronized crosslinks were developed by coupling cystamine-functionalized GO nanosheets with Fe3O4 nanoparticles modified with primary amine and methyl acrylate. These magnetic GO nanosheets were loaded with DOX to create a dual pH- and redox-responsive delivery system for cancer chemotherapy. The prepared magnetic nanosheets underwent characterization using FTIR, XRD, DLS, VSM, FE-SEM, and TEM. Physical DOX adsorption was evaluated using various isotherms, including Langmuir, Freundlich, Temkin, and Dubinin-Radushkevich. The in-vitro release profiles of DOX from the magnetic nanosheets were studied under different pH conditions, with and without glutathione (GSH), and the drug release data were fitted with various kinetic models. Additionally, an MTT assay was employed to assess the compatibility and antitumor activity of DOX-loaded magnetic nanosheets in the HepG2 cell line. The results showed that the maximum drug loading was 13.1% (w/w) at a drug/carrier ratio of 1. Without GSH addition, the maximum drug release after 10 days was only 17.9% and 24.1% at pH 7.4 and 5.3, respectively. However, in the presence of GSH, the maximum drug release reached 51.7% and 64.8% at pH 7.4 and 5.3, respectively. Finally, the research findings suggest that the magnetic nanosheets exhibited pH- and redox-stimuli drug release, high biocompatibility, and superior antitumor activity compared to free DOX.

In this study, the feasibility of preparing a calcined laterite–phosphoric acid–Fe 3 O 4 -based geopolymer is investigated and its application for immobilizing radioactive borate liquid waste (RBLW) is explored. The addition of Fe 3 O 4 enhances the compressive strength of the geopolymer and mitigates the retardation effects on the geopolymer caused by RBLW. Reactions between Fe 3 O 4 and H 3 PO 4 not only promote the geopolymerization process by generating heat and forming additional geopolymer gel, but also produce amorphous iron–phosphorus phases, contributing to higher compressive strength of the waste forms. Moreover, partial replacement of [AlO 4 ] tetrahedra with [FeO 6 ] octahedra creates stable –Fe–O–P–O–Al–O–Si– network structures. The geopolymer waste forms exhibit remarkable leaching resistance after Fe 3 O 4 addition owing to the reduced open porosity, leading to radionuclide immobilization through physical encapsulation more efficiently. Furthermore, residual Fe 3 O 4 may contribute to Co2+ immobilization through magnetic adsorption. Overall, the calcined laterite–phosphoric acid–Fe 3 O 4 -based geopolymer waste forms exhibit excellent performance in immobilizing RBLW, offering a new strategy for RBLW treatment. [ABSTRACT FROM AUTHOR]

The recyclable silver-decorated magnetic Fe3O4/tannin composites Fe3O4@TA-Ag (MFTA) were prepared by hydrothermal method and characterized by XRD, XPS, TEM, and UV–Vis techniques. The catalytic and antimicrobial activities of the MFTA composites were evaluated, and it was found that the MFTA3 composite demonstrated the highest catalytic activity for the reduction of 4-nitrophenol, with a reaction rate constant of 1.039 min−1, in comparison with the other prepared composites. Furthermore, the MFTA3 composites demonstrated significant antibacterial activity toward both Escherichia coli and Staphylococcus aureus, with inhibition zones of 13.7 and 10.2 mm, respectively. This work provides promising high-performance catalysts/bactericides in environmental remediation and antibacterial applications. [ABSTRACT FROM AUTHOR]

Realizing spin transport between heavy metal and two‐dimensional (2D) magnetic materials at high Curie temperature (TC) is crucial to advanced spintronic information storage technology. Here, environmentally stable 2D nonlayered Fe3O4 nanosheets are successfully synthesized using a reproducible process and found that they exhibit vortex magnetic domains at room temperature. A Verwey phase transition temperature (TV) of ≈110 K is identified for ≈3 nm thick nanosheet through Raman characterization and spin Hall device measurement of the Pt/Fe3O4 bilayer. The anisotropic magnetoresistance ratio decreases near TV, while both the spin Hall magnetoresistance ratio and spin mixing conductance (Gr) increase at TV. As the temperature approaches 112 K, the anomalous Hall effect ratio tends to become zero. The maximum Gr reaches ≈5 × 1015 Ω−1m−2 due to the clean and flat interface between Pt and 2D nanosheet. The observed spin transport behavior in Pt/Fe3O4 spin Hall devices indicates that 2D Fe3O4 nanosheets possess potential for high‐power micro spintronic storage devices applications. [ABSTRACT FROM AUTHOR]

We propose here a fabrication of an electrochemical sensor to detect heavy metal ions based on a glass carbon electrode (GCE) modified with a composite system consisting of graphene, chitosan, and Fe3O4 nanoparticles (GrCF) by using square wave voltammetry (SWV) measurements. The GrCF composite was characterized by scanning electron microscope (SEM), X-ray diffraction (XRD), and Raman spectroscopy. GrCF consists of thin and smooth sheets stacked in overlapping layers to form porous structures. In the GrCF composite, graphene acts as a substrate with a high electrochemical activity and a good electrical conductivity, Fe3O4 nanoparticles are uniformly distributed on the graphene thanks to chitosan as a binder, the functional groups of chitosan (− OH, − NH2) have the ability to form complexes with heavy metal ions, and the excellent adsorption capacity of Fe3O4 nanoparticles has enhanced the electrochemical reactions. The GrCF/GCE can detect Pb2+ ions with a linear range from 4 to 16 μM, a low detection limit of 3.57 μM, and a sensitivity of 8.623 μA μM−1. Furthermore, the repeatability of the measurements are reliable with a standard deviation (SD) of 0.15 μA and a relative standard deviation (RSD%) of 4.16%. Additionally, Pb2+ was detected in the real sample at potentials of − 0.50 V/ − 0.52 V with calculated recovery values for two measurements of 89.02% and 89.43%. The electrode modification method based on the GrCF composite promises outstanding advantages in the field of electrochemical sensors for detection of heavy metal ions. [ABSTRACT FROM AUTHOR]

This study examines the impact of copper oxide (CuO), iron oxide (Fe3O4), and their composite (Fe3O4@CuO) nanoparticles on harmful microorganisms in tomato plant roots and stems. The research evaluates agro-environmental factors, including soil composition, moisture levels, and temperature, that influence the efficacy of these nanoparticles. The nanoparticles prepared by the PLAL technique were subjected to structural, morphological, topographic, and optical analysis using a range of methods, including XRD, FE-SEM, EDS, AFM, and UV–Visible spectroscopy. The copper and iron composite particles were found to be polycrystalline, with the iron element present in magnetite and hematite phases. The particles exhibited a spherical form, however, there was agglomeration between them. The optical characteristics exhibited plasmon resonance peaks, indicating the transition of the materials into an optimal nanoscale phase. Both laboratory and field studies were conducted to assess their antifungal activity. The findings reveal that the Fe3O4@CuO composite exhibited superior pathogen suppression compared to the individual nanoparticles. This research offers valuable insights into the application of nanoparticles for controlling plant fungal and bacterial diseases, contributing to more effective and sustainable agricultural practices. [ABSTRACT FROM AUTHOR]

Contaminated water has remained an unsolved problem for decades, particularly when the contamination derived from heavy metals. A possible solution is to mix the contaminated water with magnetic nanoparticles so that an adsorption process can take place. In that frame, Tesla valve micromixer and Fe 3 O 4 magnetic nanoparticles were selected to perform simulations for encounter maximum mixing efficiency. These simulations focus on inlet velocities ratios between contaminated water and nanoparticles and inlet rates of nanoparticles. The maximum mixing efficiency was 44% for the inverse double Tesla micromixer found for the combination of Fe 3 O 4 nanoparticles as the inlet rate and with inlet velocity ratios of V p V c = 10 . [ABSTRACT FROM AUTHOR]

A novel composite material, magnetic chitosan-clay/benzoin/Fe3O4 (CS-CY/Benz/Fe3O4), was synthesized for effectively removing thionine dye (TH) from water solutions. The structural integrity and suitability of CS- CY/Benz/Fe3O4 composite for adsorption purposes were validated through extensive characterization techniques including BET, XRD, FTIR, and SEM. The adsorption efficiency was optimized through a Box–Behnken design (BBD) employing response surface methodology (RSM), focusing on variables such as adsorbent dose (A: 0.02–0.08 g), solution pH (B: 4–10), temperature (C: 30–60 °C), and time (D: 5–30 min). Experimental results revealed a maximum TH removal of 99% with significant interactions between temperature (C) and time (D) (p-value = 0.0001). The optimal conditions for TH removal were determined as pH ~ 5.91, adsorbent dosage of 0.08 g, temperature of 54.34 °C, and time of 29.7 min. The investigation of kinetics revealed that the adsorption process conformed to a pseudo-second-order (PSO) model, while the equilibrium data were effectively described by the Freundlich isotherm model. At a temperature of 333.15 K and a TH concentration of 350 mg/L, the adsorption capacity was determined to be 660.86 mg/g. The mechanism of adsorption encompassed various interactions such as electrostatic attractions, n–π interactions, hydrogen bonding, and Yoshida H-bonding. Particularly, the CS-CY/Benz/Fe3O4 composite demonstrated strong magnetic responsiveness, enabling straightforward separation from water using an external magnetic field after adsorption. Particularly, the CS-CY/Benz/Fe3O4 composite demonstrated strong magnetic responsiveness, enabling straightforward separation from water using an external magnetic field after adsorption. This research contributes important findings to the advancement of magnetic chitosan-based composites for efficient removal of TH dye pollutants from water environments. [ABSTRACT FROM AUTHOR]

Delivering anticancer drugs to the appropriate site within the body poses a critical challenge in cancer treatment with chemotherapeutic agents like doxorubicin (DOX). Magnetic graphene oxide (GO) nanosheets with generation 1 (G1) amidoamine-dendronized crosslinks were developed by coupling cystamine-functionalized GO nanosheets with Fe3O4 nanoparticles modified with primary amine and methyl acrylate. These magnetic GO nanosheets were loaded with DOX to create a dual pH- and redox-responsive delivery system for cancer chemotherapy. The prepared magnetic nanosheets underwent characterization using FTIR, XRD, DLS, VSM, FE-SEM, and TEM. Physical DOX adsorption was evaluated using various isotherms, including Langmuir, Freundlich, Temkin, and Dubinin-Radushkevich. The in-vitro release profiles of DOX from the magnetic nanosheets were studied under different pH conditions, with and without glutathione (GSH), and the drug release data were fitted with various kinetic models. Additionally, an MTT assay was employed to assess the compatibility and antitumor activity of DOX-loaded magnetic nanosheets in the HepG2 cell line. The results showed that the maximum drug loading was 13.1% (w/w) at a drug/carrier ratio of 1. Without GSH addition, the maximum drug release after 10 days was only 17.9% and 24.1% at pH 7.4 and 5.3, respectively. However, in the presence of GSH, the maximum drug release reached 51.7% and 64.8% at pH 7.4 and 5.3, respectively. Finally, the research findings suggest that the magnetic nanosheets exhibited pH- and redox-stimuli drug release, high biocompatibility, and superior antitumor activity compared to free DOX. [ABSTRACT FROM AUTHOR]