Search Results (439)

Lead (Pb) in soil poses serious environmental and health risks, and its removal requires complex and costly treatment methods to meet strict regulatory standards. To effectively address this challenge, innovative and efficient techniques are essential. Sepiolite-supported MnFe₂O₄ (MnFe₂O₄/SEP) composites were synthesized via a chemical co-precipitation method. The effects of MnFe₂O₄/SEP on soil pH, cation exchange capacity (CEC), available Pb content, Pb²⁺ uptake, and the activities of antioxidant enzymes in Brassica chinensis (Pak Choi) were examined. MnFe₂O₄/SEP showed superior Pb²⁺ adsorption compared to SEP alone, fitting Langmuir models, Dubinin-Radushkevich (D-R) models, Temkin models and pseudo-second-order kinetics. The maximum adsorption capacities at 298, 308, and 318 K were 459, 500 and 549 mg·g⁻¹, respectively. XPS analysis indicated that chemisorption achieved through ion exchange between Pb²⁺ and H⁺ was the main mechanism. MnFe₂O₄/SEP increased the soil pH by 0.2–1.5 units and CEC by 18–47%, while reducing available Pb by 12–83%. After treatment with MnFe₂O₄/SEP, acid-extractable and reducible Pb in the soil decreased by 14% and 39%, while oxidizable and residual Pb increased by 26% and 21%, respectively. In Brassica chinensis, MnFe₂O₄/SEP reduced Pb²⁺ uptake by 76%, increased chlorophyll content by 36%, and decreased malondialdehyde (MDA) levels by 36%. The activities of antioxidant enzymes—superoxide dismutase (SOD), peroxidase (POD), and catalase (CAT)—were decreased by 29%, 38% and 17%, respectively. These findings demonstrate that MnFe₂O₄/SEP is an efficient Pb²⁺ adsorbent that immobilizes Pb in soil mainly through ion exchange, thereby providing a highly effective strategy for remediating Pb-contaminated soils and improving plant health. Full article

This study focuses on the possibility of cleaning of industrial wastewater with catalytically active magnetic nanoparticles. Cobalt ferrite synthesized by the co-precipitation method was used, as prepared or after surface modification with a silica precursor. Electronic absorption spectra were recorded and analyzed to obtain the phenol degrading rate for various experimental design variants. Treating with pristine magnetic nanoparticles under simultaneous exposure to ultraviolet radiation resulted in similar degrading rates for 4 g/L and 8 g/L pristine nanoparticles, while, for silanized nanoparticles, the degrading rates were slightly increased. Along with ultraviolet irradiation and magnetic nanoparticles, hydrogen peroxide was also added, which led to significant enhancement of phenol degradation, for both pristine and silanized nanoparticles. It is proposed that photo-Fenton processes, triggered by metal ions at the nanoparticle surface and water photolysis and sustained by hydrogen peroxide decomposition, occurred to gradually decompose phenol to simpler compounds. Full article

Purpose: The synthesis of nanoscale particles with antibacterial properties has garnered significant attention in pharmaceutical research, driven by the escalating threat of antibiotic-resistant bacteria. This study investigates the antibacterial efficacy of Zn–Co ferrite nanoparticles against virulent, antibiotic-resistant, and biofilm-forming strains of Escherichia coli. Methods: Three nanoparticle variants—S1 (Zn_0.7Co_0.3Fe₂O₄), S2 (Zn_0.5Co_0.5Fe₂O₄), and S3 (Zn_0.3Co_0.7Fe₂O₄)—were synthesized using the solution combustion method by systematically varying the Zn:Co molar ratio. The Scanning Electron Micrograph, X-ray diffraction analysis, Complementary Fourier-transform infrared, Minimum Inhibitory Concentration, and Minimum Bactericidal Concentration were performed. Results: The SEM spectroscopy study revealed distinct morphological differences as a function of the cobalt substitution level within the spinel ferrite matrix. At the highest level of cobalt substitution (Zn_0.3Co_0.7Fe₂O₄), the microstructure displayed significant irregularities, with enhanced agglomeration and a notably broader particle size distribution. X-ray diffraction analysis confirmed the formation of crystalline structures, with an average crystallite size of 12.65 nm. Complementary Fourier-transform infrared spectroscopy revealed characteristic absorption bands in the 400–600 cm⁻¹ range, indicative of the cubic spinel structure of the ferrite nanoparticles. The higher-frequency band was associated with metal–oxide stretching in the tetrahedral sites, while the lower-frequency band corresponded to stretching in the octahedral sites. The Minimum Inhibitory Concentration and Minimum Bactericidal Concentration assays revealed that Zn–Co ferrite nanoparticles possess potent antibacterial activity against virulent, antibiotic-resistant, and biofilm-forming strains of E. coli. Conclusion: Increasing the molar ratio of Zn to Co enhances the antibacterial activity of the nanoparticles. These findings suggest that Zn–Co ferrite nanoparticles could serve as a promising alternative to conventional antibacterial agents for combating multidrug-resistant pathogenic bacteria in the future. Full article

Cancer is still the world’s most prevalent cause of death, and the limited efficacy of current treatments highlights the requirement for new therapeutic approaches. In this study, neodymium (Nd)-doped cobalt ferrite (CoFe_2₋zNd_zO₄, z = 0; 0.01; 0.02; 0.03; 0.05; 0.1) nanoparticles (Nd0-Nd5) were synthesized via the combustion method. The structural, morphological, and magnetic properties were characterized using X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), vibrating sample magnetometry (VSM), and scanning transmission electron microscopy (STEM) analysis. The synthesized compounds demonstrated single-phase spinel structures, with morphological differences observed between undoped and Nd-doped samples. The biological activity of the nanoparticles was evaluated on immortalized human keratinocytes (HaCaT) and on cancer cell lines: melanoma (A375), breast adenocarcinoma (MCF-7), and pancreatic carcinoma (PANC-1). The cytotoxic effects of Nd0-Nd5 (50–1000 μg∙mL⁻¹) were assessed through Alamar Blue and lactate dehydrogenase (LDH) release assays. The results indicated a dose-dependent cytotoxic effect in cancer cell lines. Changes in cell morphology, suggesting the induction of the apoptotic processes, were observed through immunofluorescence staining of F-actin and nuclei. These findings highlight the potential of Nd-doped cobalt ferrite nanoparticles as selective anticancer agents, warranting further investigation to fully elucidate their mechanisms of action and therapeutic applicability. Full article

Nosocomial infections caused by Candida albicans pose serious challenges to healthcare systems due to their persistence on medical surfaces and resistance to conventional disinfectants. This study evaluates antifungal properties of SnO₂ doped with silver and cuprite nanoparticles and WO₃ thin films, as well as cobalt (CoFe₂O₄) and cobalt–nickel (Co_0.5Ni₀.₅Fe₂O₄) ferrite nanoparticles, activated by ultraviolet C (UVC) radiation, direct electric current (up to 100 V), and magnetic fields. SnO₂ films were synthesized by Spray Pyrolysis and WO₃ by Sputtering deposition, Ferrites nanoparticles by sol–gel, while metallic nanoparticles were synthetized via chemical reduction. Characterization consisted mainly of SEM, TEM, and XRD, and their antimicrobial activity was tested against C. albicans. WO₃ films achieved 86.2% fungal inhibition after 5 min of UVC exposure. SnO₂ films doped with nanoparticles reached 100% inhibition when combined with UVC and 100 V. Ferrite nanoparticles alone showed moderate activity (21.9%–40.4%) but exhibited strong surface adhesion to fungal cells, indicating potential for magnetically guided antifungal therapies. These results demonstrate the feasibility of using multifunctional nanomaterials for rapid, non-chemical disinfection. The materials are low-cost, scalable, and adaptable to hospital settings, making them promising candidates for reducing healthcare-associated fungal infections through advanced surface sterilization technologies. Full article

This study introduces an efficient and sustainable catalytic system utilizing cobalt ferrite nanoparticles (CoFe₂O₄-NPs) for the synthesis of valuable 6-amino-2-oxo-4-phenyl (or 4-chlorophenyl)-1,2,3,4-tetrahydropyrimidine-5-carbonitrile derivatives. Recognizing the limitations of traditional methods for the Biginelli reaction, we thoroughly characterized CoFe₂O₄-NPs, alongside individual iron oxide nanoparticles (Fe₂O₃-NPs) and cobalt oxide nanoparticles (CoO-NPs), using FTIR, XRD, TEM, SEM, XPS, TGA, and BET analysis. These characterizations revealed the unique structural, morphological, and physicochemical properties of CoFe₂O₄-NPs, including an optimized porous structure and significant bimetallic synergy between Fe and Co ions. Catalytic studies demonstrated that CoFe₂O₄-NPs significantly outperformed individual Fe₂O₃-NPs and CoO-NPs under mild conditions. While the latter only catalyzed the Knoevenagel condensation, CoFe₂O₄-NPs uniquely facilitated the complete Biginelli reaction. This superior performance is attributed to the synergistic electronic environment within CoFe₂O₄-NPs, which enhances reactant activation, intermediate stabilization, and proton transfer during the multi-step reaction. This work highlights the potential of CoFe₂O₄-NPs as highly efficient and selective nanocatalysts for synthesizing biologically relevant 1,2,3,4-tetrahydropyrimidines, offering a greener synthetic route in organic chemistry. Full article

Co_0.95R_0.05Fe₂O₄ nanoparticles were synthesized using a sol-gel approach incorporating bio-based agents and were found to be single phases adopting a cubic Fd-3m structure. XPS shows the presence of Gd³⁺ and Ho³⁺ ions. The spin–orbit splitting of about 15.4 eV observed in Co 2p core-level spectra is an indication that Co is predominantly present as Co³⁺ state, while the satellite structures located at about 6 eV higher energies than the main lines confirm the existence of divalent Co in Co_0.95R_0.05Fe₂O₄. The positions of the Co 3s and Fe 3s main peaks obtained by curve fitting and the exchange splitting obtained values for Co 3s and Fe 3s levels point to the high Co³⁺/Co²⁺ and Fe³⁺/Fe²⁺ ratios in both samples. The saturation magnetizations are smaller for the doped samples compared to the pristine ones. For theoretical magnetization calculation, we have considered that the heavy rare earths are in octahedral sites and their magnetic moments are aligned antiparallelly with 3d transition magnetic moments. ZFC-FC curves shows that some nanoparticles remain superparamagnetic, while the rest are ferrimagnetic, ordered at room temperature, and showing interparticle interactions. The M_S/Ms ratio at room temperature is below 0.5, indicating the predominance of magnetostatic interactions. Full article

Co_0.95R_0.05Fe₂O₄ nanoparticles with R = La, Pr, Nd, Sm, and Eu were synthesized via an environmentally friendly sol–gel method. The prepared samples were studied using X-ray diffraction measurements (XRD), transmission electron microscopy (TEM), X-ray photoelectron microscopy (XPS), and magnetic measurements. All compounds were found to be single phases adopting a cubic Fd-3m structure. EDS analysis confirmed the presence of Co, Fe, R, and oxygen in all cases. The XPS measurements reveal that the Co 2p core-level spectra are characteristic for Co³⁺ ions, as indicated by the 2p_3/2 and 2p_1/2 binding energies and spin–orbit splitting values. The analysis of the Fe 2p core-level spectra reveals the presence of both Fe³⁺ and Fe²⁺ ions in the investigated samples. The doped samples exhibit lower saturation magnetizations than the pristine sample. Very good agreement with the saturation magnetization values was obtained if we assumed that the light rare-earth ions occupy octahedral sites and their magnetic moments align parallel to those of the 3d transition metal ions. The ZFC-FC curves indicate that some nanoparticles remain superparamagnetic, while others exhibit ferrimagnetic ordering at room temperature, suggesting the presence of interparticle interactions. The M_r/M_s ratio at room temperature reflects the dominance of magnetostatic interactions. Full article

In this study, chromium ferrite (FeCr; CrFe₂O₄) nanoparticles supported on activated carbon (AC), obtained from agricultural olive mill solid waste, were synthesized via a simple hydrothermal process. The structural, morphological, optical, and chemical properties of the FeCr/AC composite were characterized using XRD, SEM, EDX, DRS, BET, and FTIR techniques. The FeCr/AC composite was applied as a heterogeneous photo-Fenton catalyst for the degradation of methylene blue (MB) dye in an aqueous solution under 25 W visible-light LED irradiation. Critical operational factors, such as FeCr/AC dosage, pH, MB concentration, and H₂O₂ levels, were optimized. Under optimal conditions, 97.56% of MB was removed within 120 min of visible-light exposure, following pseudo-first-order kinetics. The composite also exhibited high efficiency in degrading methyl orange dye (95%) and tetracycline antibiotic (88%) within 180 min, with corresponding first-order rate constants of 0.0225 min⁻¹ and 0.0115 min⁻¹, respectively. This study highlights the potential of FeCr/AC for treating water contaminated with dyes and pharmaceuticals, in line with the Sustainable Development Goals (SDGs) for water purification. Full article

In the present study, we synthesized fluorocarbon-coated cobalt ferrite (CoFe₂O₄) magnetic nanoparticles using alkoxysilanes such as trimethoxy(3,3,3-trifluoropropyl)silane (TFPTMS), trimethoxy(1H,1H,2H,2H-nonafluorohexyl)silane (NFHTMS), and triethoxy(1H,1H,2H,2H-perfluorodecyl)silane (PFDTES). The synthesized nanoparticles were characterized by various techniques, including X-ray diffractometry (XRD), transmission electron microscopy (TEM/HRTEM/EDXS), Fourier transform infrared spectroscopy (FTIR), specific surface area measurements (BET), and magnetometry (VSM). To understand their surface characteristics, contact angle (CA) measurements were carried out, providing valuable insights into their hydrophobic properties. Among the samples of CoFe₂O₄ coated with fluoroalkoxysilanes, those with PFDTES surface coating had the highest water contact angle of 159.2°, indicating their superhydrophobic character. The potential of the prepared fluoroalkoxysilane-coated CoFe₂O₄ nanoparticles for the removal of waste low-SAPS synthetic engine oil from a model aqueous solution was evaluated based on three key parameters: adsorption efficiency (%), adsorption capacity (mg/g), and desorption efficiency (%). All synthesized CoFe₂O₄ samples coated with fluoroalkoxysilane showed high oil adsorption efficiency, ranging from 87% to 98%. The average oil adsorption capacity for the samples was as follows: F₃-SiO₂@CoFe₂O₄ (3.1 g of oil/g of adsorbent) > F₉-SiO₂@CoFe₂O₄ (2.7 g of oil/g of adsorbent) > F₁₇-SiO₂@CoFe₂O₄ (1.5 g of oil/g of adsorbent) as a result of increasing oleophobicity with increasing fluorocarbon chain length. The desorption results, which showed 77–97% oil recovery, highlighted the possibility of reusing the adsorbents in multiple adsorption/desorption cycles. Full article

This study reports the synthesis and characterization of Co_xNi_1−xFe₂O₄ (x = 0, 0.2, 0.4, 0.6, 0.8, 1) nanoparticles using a co-precipitation method. In this approach, metal ions are precipitated in the presence of a stabilizing agent, which is a common and effective method for nanoparticle preparation. The microstructure and magnetic properties were studied after calcination at 600 °C and heat treatment at 1000 °C. X-ray diffraction (XRD) and Fourier transform infrared (FTIR) spectroscopy confirmed the formation of a single-phase spinel structure. The average crystallite size, calculated using the (311) diffraction peak and the Scherrer equation, ranged from 13 to 19 nm. Scanning electron microscopy (SEM) showed that the nanoparticles had a spherical morphology. Thermogravimetric and differential thermal analysis (TG-DTA) revealed a three-step weight loss process. Magnetic measurements, including remanent magnetization, saturation magnetization, and coercivity, were performed using a vibrating sample magnetometer (VSM) at room temperature. The replacement of Ni²⁺ with Co²⁺ enhanced the magnetic properties, resulting in increased magnetic moment and anisotropy. These effects are attributed to changes in cation distribution, exchange interactions, surface effects, and magnetocrystalline anisotropy. Overall, Co²⁺ doping improved the magnetic behavior of nickel ferrite, indicating its potential for application in memory devices and magnetic recording media. Full article

Acetone detection is crucial for non-invasive health monitoring and environmental safety, so there is an urgent demand to develop high-performance gas sensors. Here, platinum (Pt)-functionalized layered flower-like nickel ferrite (NiFe₂O₄) sheets were efficiently fabricated via facile hydrothermal synthesis and wet chemical reduction processes. When the Ni/Fe molar ratio is 1:1, the sensing material forms a Ni/NiO/NiFe₂O₄ composite, with performance further optimized by tuning Pt loading. At 1.5% Pt mass fraction, the sensor shows a high acetone response (R_g/R_a = 58.33 at 100 ppm), a 100 ppb detection limit, fast response/recovery times (7/245 s at 100 ppm), and excellent selectivity. The enhancement in performance originates from the synergistic effect of the structure and Pt loading: the layered flower-like morphology facilitates gas diffusion and charge transport, while Pt nanoparticles serve as active sites to lower the activation energy of acetone redox reactions. This work presents a novel strategy for designing high-performance volatile organic compound (VOC) sensors by combining hierarchical nanostructured transition metal ferrites with noble metal modifications. 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 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

In this work, we synthesized the Co_0.85Bi_0.15Fe_1.9X_0.1O₄ (X = Ce³⁺, Sm³⁺, Ho³⁺, and Er³⁺) nanoparticles via the auto-combustion method. The cell viability against two breast cancer cells (MDA-MB-231 and T-47D cells) and the PC3 prostate cancer cells were carefully analyzed and correlated with the structural parameters and particle size values as well as the chemical composition. The produced compounds’ morphological and structural characteristics were performed using scanning transmission microscopy (TEM) and X-ray Diffraction (XRD). For all compounds, the analyses of the XRD experimental data revealed a structurally reversed cubic spinel with space group Fd-3m. All of the compounds had crystallites smaller than 45 nm which concorded well with the particle size values deduced from TEM images. Co_0.85Bi_0.15Fe_1.9Ho_0.1O₄ nanoparticles induced a high mortality of breast and prostate cancer cells (MDA-MB-231, T-47D, and PC3) while the Co_0.85Bi_0.15Fe_1.9Sm_0.1O₄ compound (higher particle size) reduced almost 35% of MDA-MB-231 cancer cells. With very low cytotoxicity against normal human cells, the Co_0.85Bi_0.15Fe_1.9Ho_0.1O₄ nanoparticles play a significant role in the elimination of cancer cells. Full article