Search Results (110)

Background/Objectives: Magnetic nanoparticles, particularly iron oxide-based materials, such as magnetite (Fe₃O₄), have gained significant attention as contrast agents in medical imaging This study aimsto syntheze and characterize Fe₃O₄-based core–shell nanostructures, including Fe₃O₄@TiO₂ and Fe₃O₄@SiO₂, and to evaluate their potential as tunable contrast agents for diagnostic imaging. Methods: Fe₃O₄, Fe₃O₄@TiO₂, and Fe₃O₄@SiO₂ nanoparticles were synthesized via co-precipitation at varying temperatures from iron salt precursors. Fourier transform infrared spectroscopy (FTIR) was used to confirm the presence of Fe–O bonds, while X-ray diffraction (XRD) was employed to determine the crystalline phases and estimate average crystallite sizes. Morphological analysis and particle size distribution were assessed by scanning electron microscopy with energy-dispersive X-ray spectroscopy (SEM-EDX) and transmission electron microscopy (TEM). Magnetic properties were investigated using vibrating sample magnetometry (VSM). Results: FTIR spectra exhibited characteristic Fe–O vibrations at 543 cm⁻¹ and 555 cm⁻¹, indicating the formation of magnetite. XRD patterns confirmed a dominant cubic magnetite phase, with the presence of rutile TiO₂ and stishovite SiO₂ in the coated samples. The average crystallite sizes ranged from 24 to 95 nm. SEM and TEM analyses revealed particle sizes between 5 and 150 nm with well-defined core–shell morphologies. VSM measurements showed saturation magnetization (Ms) values ranging from 40 to 70 emu/g, depending on the synthesis temperature and shell composition. The highest Ms value was obtained for uncoated Fe₃O₄ synthesized at 94 °C. Conclusions: The synthesized Fe₃O₄-based core–shell nanomaterials exhibit desirable structural, morphological, and magnetic properties for use as contrast agents. Their tunable magnetic response and nanoscale dimensions make them promising candidates for advanced diagnostic imaging applications. Full article

In this study, we report the development of a novel magnetized coal fly ash-supported nano-silver composite (AgNPs/MCFA) for dual-functional applications in wastewater treatment: the efficient degradation of methyl orange (MO) dye and broad-spectrum antibacterial activity. The composite was synthesized via a facile impregnation–reduction–sintering route, utilizing sodium citrate as both a reducing and stabilizing agent. The AgNPs/MCFA composite was systematically characterized through multiple analytical techniques, including Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), and vibrating sample magnetometry (VSM). The results confirmed the uniform dispersion of AgNPs (average size: 13.97 nm) on the MCFA matrix, where the formation of chemical bonds (Ag-O-Si) contributed to the enhanced stability of the material. Under optimized conditions (0.5 g·L⁻¹ AgNO₃, 250 °C sintering temperature, and 2 h sintering time), AgNPs/MCFA exhibited an exceptional catalytic performance, achieving 99.89% MO degradation within 15 min (pseudo-first-order rate constant k_a = 0.3133 min⁻¹) in the presence of NaBH₄. The composite also demonstrated potent antibacterial efficacy against Escherichia coli (MIC = 0.5 mg·mL⁻¹) and Staphylococcus aureus (MIC = 2 mg·mL⁻¹), attributed to membrane disruption, intracellular content leakage, and reactive oxygen species generation. Remarkably, AgNPs/MCFA retained >90% catalytic and antibacterial efficiency after five reuse cycles, enabled by its magnetic recoverability. By repurposing industrial waste (coal fly ash) as a low-cost carrier, this work provides a sustainable strategy to mitigate nanoparticle aggregation and environmental risks while enhancing multifunctional performance in water remediation. Full article

A novel type of multifunctional hybrid membranes combining modified chitosan, functionalized multi-walled carbon nanotubes (MWCNTs), and rare earth element ion-imprinted polymers (REEIIPs) were designed and characterized. The synthesized materials were characterized by thermogravimetric analysis (TGA), scanning electron microscopy (SEM), vibrating sample magnetometry (VSM), X-ray diffraction (XRD), X-ray micro-tomography, and Fourier transform infrared spectroscopy (FTIR). The hybrid membranes were also studied in terms of their mechanical and rheological properties. The key element of the proper preparation of hybrid membranes using the casting method in an external magnetic field was to synthesize membrane components with appropriate magnetic properties. It was found that they showed tunable weak ferromagnetic properties, and the increase in modified nanotube addition caused the rise in the membrane’s saturation magnetization, which for Nd-selective hybrid membranes reached 0.44 emu/g. Also, the increase in thermooxidative stability was noted after introducing functionalized nanotubes into polymer matrices, which, in the case of Gd-selective membranes, were stable even up to 730 °C. The rise in the modified MWCNT addition and selection of appropriate REE ion-imprinted polymers improved mechanical (Rm and E values increase even twice) and rheological parameters (almost double growth of E′ and E″ values) of the tested membranes. Synthesized hybrid membranes showed a high rejection of matrix components and an increase in retention ratio with rising MWCNT-REEIIP addition, ultimately reaching 94.35%, 92.12%, and 90.11% for Nd, Pr, and Gd, respectively. The performed analysis confirmed homogeneous dispersion, phase compatibility, network integration, formation of a complex 3D microstructure, and improved operational stability of created hybrid membranes, which is significant for their future applications in Nd, Pr, and Gd recovery from coal fly ash extracts. Full article

A simple and innovative synthesis strategy was established to produce polymer microspheres with a distinctive walnut-like morphology, incorporating Fe₃O₄ nanoparticles within their structure. This was achieved through γ-ray-initiated mini-emulsion polymerization. To ensure high encapsulation efficiency, the surface of the Fe₃O₄ nanoparticles was chemically altered to shift their wettability from hydrophilic to hydrophobic, enabling uniform dispersion within the monomer phase before polymerization. The formation of the walnut-like architecture was found to be significantly influenced by both the polymerization dynamics and phase separation, as well as the shrinkage of the crosslinked polymer network formed between the monomer and the resulting polymer. Divinylbenzene (DVB) was chosen as the monomer due to its ability to generate a mechanically stable polymer framework. The γ-ray irradiation effectively initiated polymerization while preserving structural coherence. A detailed analysis using FTIR, SEM, and TEM confirmed the successful fabrication of the Fe₃O₄-loaded polymer microspheres with their characteristic textured surface. Moreover, magnetic characterization via vibrating sample magnetometry (VSM) indicated pronounced superparamagnetic behavior and strong magnetic responsiveness, highlighting the potential of these microspheres for advanced biomedical applications. Full article

Superparamagnetic magnetite nanoparticles (Fe₃O₄) have garnered considerable interest due to their unique magnetic properties and potential for integration into multifunctional biomaterials. In particular, their incorporation into bacterial cellulose (BC) matrices offers a promising route for developing sustainable and high-performance magnetic composites. Numerous studies have explored BC-magnetite systems; however, innovations combining ex situ coprecipitation synthesis within BC matrices, tailored reagent molar ratios, stirring protocols, and purification processes remain limited. This study aimed to optimize the ex situ coprecipitation method for synthesizing superparamagnetic magnetite nanoparticles embedded in BC membranes, focusing on enhancing particle stability and crystallinity. BC membranes containing varying concentrations of magnetite (40%, 50%, 60%, and 70%) were characterized using X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and vibrating sample magnetometry (VSM). The resulting magnetic BC membranes demonstrated homogenous dispersion of nanoparticles, improved crystallite size (6.96 nm), and enhanced magnetic saturation (Ms) (50.4 emu/g), compared to previously reported methods. The adoption and synergistic optimization of synthesis parameters—unique to this study—conferred greater control over the physicochemical and magnetic properties of the composites. These findings position the optimized BC-magnetite nanocomposites as highly promising candidates for advanced applications, including electromagnetic interference (EMI) shielding, electronic devices, gas sensors, MRI contrast agents, and targeted drug delivery systems. Full article

The increasing prevalence of antimicrobial resistance alongside the pharmacological limitations and adverse effects associated with conventional antibiotics necessitates the development of novel and efficacious antimicrobial agents. In this study, magnetic iron oxide nanoparticles (MIONPs) were synthesized via a chemical co-precipitation method. Activated carbon (AC) derived from Hibiscus esculentus (HE) fruit was coated onto the nanoparticle surfaces to fabricate MIONPs/HEAC nanocomposites. To augment their antimicrobial properties, silver ions were chemically reduced and deposited onto the MIONPs/HEAC surface, yielding MIONPs/HEAC@Ag nanocomposites. Comprehensive characterization of the synthesized nanocomposites was performed using scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), vibrating sample magnetometry (VSM), dynamic light scattering (DLS), and zeta potential analysis. DLS measurements indicated average particle sizes of approximately 122 nm and 164 nm for MIONPs/HEAC and MIONPs/HEAC@Ag, respectively. Saturation magnetization values were determined to be 73.6 emu/g for MIONPs and 65.5 emu/g for MIONPs/HEAC. Antibacterial assays demonstrated that MIONPs/HEAC@Ag exhibited significant inhibitory effects against Escherichia coli ATCC 25922 and Staphylococcus aureus ATCC 25923, with inhibition zone diameters of 11.50 mm and 13.00 mm, respectively. In contrast, uncoated MIONPs/HEAC showed negligible antibacterial activity against both bacterial strains. These findings indicate that MIONPs/HEAC@Ag nanocomposites possess considerable potential as antimicrobial agents for biomedical applications, particularly in addressing infections caused by antibiotic-resistant bacteria. Full article

Magnetic zeolite nanocomposites (NCs) have emerged as a promising class of hybrid materials that combine the high surface area, porosity, and ion exchange capacity of zeolites with the magnetic properties of nanoparticles (NPs), particularly iron oxide-based nanomaterials. This review provides a comprehensive overview of the synthesis, characterization, and diverse applications of magnetic zeolite NCs. We begin by introducing the fundamental properties of zeolites and magnetic nanoparticles (MNPs), highlighting their synergistic integration into multifunctional composites. The structural features of various zeolite frameworks and their influence on composite performance are discussed, along with different interaction modes between MNPs and zeolite matrices. The evolution of research on magnetic zeolite NCs is traced chronologically from its early stages in the 1990s to current advancements. Synthesis methods such as co-precipitation, sol–gel, hydrothermal, microwave-assisted, and sonochemical approaches are systematically compared, emphasizing their advantages and limitations. Key characterization techniques—including X-Ray Powder Diffraction (XRD), Fourier Transform Infrared Spectroscopy (FTIR), Scanning and Transmission Electron Microscopy (SEM, TEM), Thermogravimetric Analysis (TGA), Nitrogen Adsorption/Desorption (BET analysis), Vibrating Sample Magnetometry (VSM), Zeta potential analysis, Inductively Coupled Plasma Optical Emission Spectroscopy (ICP-OES), and X-Ray Photoelectron Spectroscopy (XPS)—are described, with attention to the specific insights they provide into the physicochemical, magnetic, and structural properties of the NCs. Finally, the review explores current and potential applications of these materials in environmental and biomedical fields, focusing on adsorption, catalysis, magnetic resonance imaging (MRI), drug delivery, ion exchange, and polymer modification. This article aims to provide a foundation for future research directions and inspire innovative applications of magnetic zeolite NCs. Full article

Nanotechnology has emerged as a highly focused field of research due to the unique properties of nanometric materials, particularly their large specific surface areas and excellent adsorption capabilities. This study investigated the synthesis of materials based on graphene oxide (GO) functionalized with different metal oxides (MnO₂, Fe₃O₄, CuO, NiO), with potential applications in water decontamination. The morphological, structural, and compositional properties of these nanocomposites were extensively characterized using different experimental techniques, including X-ray diffraction (XRD), transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), and vibrating sample magnetometry (VSM) for magnetic property evaluation. Preliminary adsorption tests were performed for the removal of pesticides and drugs from aqueous solutions. The synthesized materials demonstrated a higher affinity for selected pesticides compared to drugs. The best removal efficiencies were 98.59% for cymoxanil, 97.93% for triadimefon, 63.33% for sulfamethoxazole, and 99.59% for diclofenac. The results indicate that the functionalization of GO with metal oxides modifies the material’s structure, increasing its potential for environmental applications such as water purification. Full article

In this study, praseodymium-doped cobalt ferrite nanoparticles (CoFe_2−yPr_yO₄, y = 0–0.2) were synthesized via sol-gel auto-combustion and systematically characterized to assess their structural, morphological, magnetic, and biological properties. X-ray diffraction (XRD) confirmed single-phase cubic cobalt ferrite formation for samples with y ≤ 0.05 and the emergence of a secondary orthorhombic PrFeO₃ phase at higher dopant concentrations. FTIR spectroscopy identified characteristic metal–oxygen vibrations and revealed a progressive shift of absorption bands with increasing praseodymium (Pr) content. Vibrating sample magnetometry (VSM) demonstrated a gradual decline in saturation (Ms) and remanent (Mr) magnetization with Pr doping, an effect further intensified by cyclodextrin surface coating. TEM analyses revealed a particle size increase correlated with dopant level, while SEM images displayed a porous morphology typical of combustion-synthesized ferrites. In vitro cell viability assays showed minimal toxicity in normal human keratinocytes (HaCaT), while significant antiproliferative activity was observed against human cancer cell lines A375 (melanoma), MCF-7 (breast adenocarcinoma), and HT-29 (colorectal adenocarcinoma), particularly in Pr 6-CD and Pr 7-CD samples. These findings suggest that Pr substitution and cyclodextrin coating can effectively modulate the physicochemical and anticancer properties of cobalt ferrite nanoparticles, making them promising candidates for future biomedical applications. Full article

The effects of the La element and heat treatment on the phase composition and magnetic properties of SmFe₁₀V₂ melt-spun ribbons are studied by X-ray diffraction (XRD) and vibrating sample magnetometry (VSM). The XRD results show that the Sm_1−xLa_xFe₁₀V₂ (x = 0, 0.2, 0.4) and SmLa_yFe₁₀V₂ (y = 0.1, 0.2, 0.3) melt-spun ribbons are composed of the 1:12 main phase with a ThMn₁₂ structure, α-Fe phase and α-La phase, and the phase formation of the SmLa_0.2Fe₁₀V₂ melt-spun ribbon is not changed after annealing at different temperatures (700–900 °C) and times (10–60 min). The XRD results indicate that La substitution in Sm_1−xLa_xFe₁₀V₂ ribbons has a negative effect on the formation of the 1:12 main phase, while the addition of a small amount of La into SmLa_yFe₁₀V₂ ribbons does not affect the formation of the 1:12 main phase. The VSM measurements show that La substitution would result in decreases in the magnetic properties of Sm_1−xLa_xFe₁₀V₂ ribbons. With the increase in La substitution, the coercivity of the ribbon decreases to 2.7 kOe with x = 0.2 and 0.43 kOe with x = 0.4. However, the magnetic properties of SmLa_yFe₁₀V₂ ribbons with a small amount of La (y = 0.2) are improved. Furthermore, the experimental results for the SmLa_0.2Fe₁₀V₂ ribbon after different heat treatments show that the magnetic properties become better initially and then become worse. Finally, the best magnetic properties (H_cj = 5.12 kOe, B_r = 6.89 kGs, M_r/M_s = 0.75, (BH)_max = 6.78 MGOe) for the SmLa_0.2Fe₁₀V₂ ribbon are obtained after annealing at 800 °C for 10 min. Full article

In this work, a newly developed magnetic molecularly imprinted Fe₃O₄/SiO₂/TiO₂/MIP photocatalyst with diclofenac (DIC) as the template was prepared by microwave-assisted synthesis. The molecularly imprinted TiO₂ layer has specific cavities designed for the DIC target molecule (imprint), resulting in a synergistic effect of extraction by adsorption and photocatalysis. For reference, non-imprinted magnetic nanoparticles (Fe₃O₄/SiO₂/TiO₂) were prepared using the same procedure. The obtained particles were characterized by X-ray diffraction analysis (XRD), Fourier transform infrared spectroscopy (FTIR), SEM-EDX, vibrating-sample magnetometry (VSM) and diffuse reflectance spectroscopy (DRS). Specific surface area, pore volume and pore size distribution were evaluated using Brunauer–Emmett–Teller (BET) adsorption–desorption isotherms. The synergistic effect of adsorption and photocatalysis as well as the kinetics and mechanism of DIC degradation using Fe₃O₄/SiO₂/TiO₂/MIP and Fe₃O₄/SiO₂/TiO₂ were determined and analysed. The adsorption efficiency of Fe₃O₄/SiO₂/TiO₂/MIP for DIC (10 mg dm⁻³) was around 86% after 60 min. The DIC (10 mg dm⁻³) removal efficiency of Fe₃O₄/SiO₂/TiO₂/MIP was around 80% after 30 min adsorption and 120 min of reaction under both UV-A- and solar-simulated light irradiation. Full article

This study employed an in-situ displacement technique to eliminate the oxide layer present on the surface of micron aluminum (μAl). Utilizing the exposed metallic aluminum, we facilitated the displacement of copper and nickel nanoparticles. These nanoparticles, approximately 90 nanometers in size, were densely adhered to the surface of the μAl particles. The elemental composition and structural characteristics of the composite particles were meticulously analyzed using Scanning Electron Microscopy (SEM), X-Ray Diffraction (XRD), Energy Dispersive Spectroscopy (EDS), Vibrating Sample Magnetometry (VSM), and X-Ray Photoelectron Spectroscopy (XPS). Subsequently, thermal analysis and combustion performance assessments were conducted to elucidate the catalytic effects of the composite particles ([nCu+nNi]/μAl) on the thermal decomposition and combustion efficiency of ammonium perchlorate (AP). The results elucidate that the nanoparticles immobilized on the surface of μAl are unequivocally metallic copper (nCu) and metallic nickel (nNi). Following the application of nCu and nNi, the oxidation reaction of μAl accelerated by nearly 400 °C; furthermore, the incorporation of [nCu+nNi]/μAl raised the thermal decomposition peak temperature of AP by approximately 130 °C. Notably, the thermal decomposition activation energy of raw AP reached as high as 241.7 kJ/mol; however, upon doping with [nCu+nNi]/μAl, this activation energy significantly diminished to 161.4 kJ/mol. The findings of the combustion experiments revealed that both the raw AP and the AP modified solely with μAl were impervious to ignition via the hot wire method. In contrast, the AP doped with [nCu+nNi]/μAl demonstrated pronounced combustion characteristics, achieving an impressive peak flame temperature of 1851 °C. These results substantiate that the nCu and nNi, when deposited on the surface of μAl, not only facilitate the oxidation and combustion of μAl but also significantly enhance the thermal decomposition and combustion dynamics of ammonium perchlorate. Consequently, the [nCu+nNi]/μAl composite shows considerable promise for application in high-burn-rate hydroxyl-terminated polybutadiene (HTPB) propellants. Full article

Co-based amorphous wires (Co-AWs) are functional materials renowned for their high impedance change rate in magnetic fields and a pronounced giant magnetoimpedance (GMI) effect. In this study, magnetron sputtering (MS) and dip-coating (DC) techniques were employed to fabricate carbon-based nanocoatings aimed at modulating the GMI properties of Co-AWs. The magnetic properties and GMI responses of the composite Co-AWs with carbon-based coatings were comparatively analyzed. The results demonstrate that both methods effectively enhanced the GMI properties of the coated Co-AWs. The DC method emerged as a rapid and efficient approach for forming the coated film, achieving a modest enhancement in GMI performance (10% enhancement). In contrast, the MS technique proved more effective in improving the GMI effect, yielding superior results. Co-AWs coated via Ms exhibited smoother surfaces and reduced coercivity. Notably, the GMI effect increased with the thickness of the sputtered carbon coatings, reaching a maximum GMI effect of 522% (a remarkable 357% enhancement) and a sensitivity of 33.8%/Oe at a coating thickness of 334 nm. The observed trend in the GMI effect with carbon layer thickness corresponded closely to variations in transverse permeability, as determined by vibrating sample magnetometry (VSM). Furthermore, the carbon coating induced changes in the initial quenching stress on the surface of the Co-AWs, leading to alterations in impedance and a significant reduction in the characteristic frequency of the Co-AWs. Our findings provide valuable insights into the modulation of GMI properties in Co-AWs, paving the way for their optimized application in advanced magnetic sensor technologies. Full article

Background/Objectives: Magnetic hyperthermia (MH) has emerged as a promising alternative to conventional cancer treatments, offering targeted tumor destruction with minimal damage to healthy tissues. In this study, we synthesized manganese-doped magnetic nanoflowers (Mn-NFs) using a polyol-mediated approach to enhance heating efficiency and biocompatibility for MH applications. Our objective was to evaluate their structural, magnetic, and in vitro hyperthermic properties to determine their potential for lung cancer therapy. Methods: Mn-NFs, with the general formula MnxFe₃-xO₄ (x = 0, 0.3, 0.5, 0.7), were synthesized via a one-step polyol method and characterized using transmission electron microscopy (TEM), X-ray diffraction (XRD), and vibrating sample magnetometry (VSM). Their heating efficiency was assessed through specific absorption rate (SAR) measurements in aqueous and solid environments under an alternating magnetic field (AMF). Cytocompatibility was evaluated using the Alamar Blue assay on A549 lung carcinoma cells. Cellular uptake was quantified via a colorimetric iron determination method, while in vitro MH efficacy was tested by subjecting Mn-NF-loaded A549 cells to AMF exposure at different field strengths and nanoparticle concentrations. Results: Mn-NFs exhibited a flower-like morphology with enhanced magnetic properties, achieving high SAR values, particularly in immobilized conditions. Cytotoxicity assays confirmed high biocompatibility at relevant doses, with Mn-NFs of x = 0.3 showing optimal cellular uptake. MH studies demonstrated significant cancer cell death at AMF intensities of around 30 kA/m, with increased effectiveness following static magnetic field pre-alignment. Conclusions: The results highlight Mn-NFs, particularly those with a Mn content of x = 0.3, as promising candidates for MH-based lung cancer therapy, combining high heating efficiency, biocompatibility, and effective intracellular uptake. Further studies are needed to validate their therapeutic potential in vivo. Full article

This study explores a sustainable approach to developing magnetic nanocomposites by synthesizing a mixed-phase iron oxide (IO) and recycled polyamide (RPA) composite from textile waste. The RPA/IO nanocomposite’s microstructural and magnetic properties were characterized using X-ray diffraction (XRD) with Rietveld refinement, scanning, transmission electron microscopy (SEM, TEM), and vibrating sample magnetometry (VSM). The proportions of the Fe₃O₄ and γ-Fe₂O₃ phases were found to be 23.2 wt% and 76.8 wt%, respectively. SEM and TEM showed a porous, agglomerated IO surface morphology with an average particle size of 14 nm. Magnetic analysis revealed ferrimagnetic and superparamagnetic behavior, with VSM showing saturation magnetization values of 21.81 emu g⁻¹ at 5 K and 18.84 emu g⁻¹ at 300 K. Anisotropy constants were estimated at 4.28 × 10⁵ and 1.53 × 10⁵, respectively, for IO and the composite, with a blocking temperature of approximately 178 K at 300 K. These results contribute to understanding the magnetic behavior of IO and their nanocomposites, which is crucial for their potential applications in emerging technologies. Full article