High Saturation Magnetization Research Articles

Insulation coating via hydrothermal oxidation for high-frequency FeSiAl soft magnetic composites

Soft magnetic composites (SMCs) play a crucial role in electronic devices owing to their high saturation magnetization. However, conventional insulation methods employed in SMCs exhibit inadequate insulation reliability, thereby restricting their further application in high frequencies. In this study, hydrothermal oxidation is introduced for insulation coating in the preparation of FeSiAl SMCs. When treated at 150 ℃ for 2 h, an insulation layer comprising of Al2O3, SiO2, Fe3O4 and Fe2O3 is formed on the surface of FeSiAl. The most optimal sample is achieved with saturation magnetization of 134.3 emu/g, presenting no significant reduction in saturation magnetization compared to the untreated sample. Cut-off frequency exceeding 300 MHz, and power loss of 503.7 kW/m3 (@7 MHz, 5 mT) are also obtained. This study suggests that hydrothermal oxidation could be a dependable method for fabricating high-frequency SMCs.

Efficient adsorptive removal of 2,4-dichlorophenoxyacetic acid (2,4-D) using biomass derived magnetic activated carbon nanocomposite in synthetic and simulated agricultural runoff water

This study focused on evaluating the efficacy of a magnetic activated carbon material (CPAC@Fe3O4) derived from pods of copper pod tree in adsorbing the toxic herbicide, 2,4- (2,4-D) from aqueous solutions. The synthesized CPAC@Fe3O4 adsorbent, underwent various characterization techniques. FESEM images indicated a rough surface, incorporating iron oxide nanoparticles, while EDS analysis confirmed the presence of elements like Fe, O, and C. Notably, the CPAC@Fe3O4 exhibited high surface area (749.10 m2/g) and pore volume (0.5351 cm³/g), confirming its mesoporous nature. XRD investigations identified distinct signals associated with graphitic carbon and magnetite nanoparticles, while VSM analysis verified its magnetic properties with a high magnetic saturation value (2.72 emu/g). The adsorption process was exothermic, with a decrease in adsorption capacity at higher temperatures. Freundlich isotherm provided the best fit for the adsorption, and the pseudo-second-order equation effectively described the kinetics. Remarkably, the maximum adsorption capacity ranged from 246.43 to 261.03 mg/g, surpassing previously reported values. The ΔH° value (−8.67 kJ/mol) suggested a physisorption mechanism, and the negative ΔG° values established the spontaneous nature. Furthermore, the synthesized adsorbent demonstrated exceptional reusability, allowing for up to five cycles of adsorption-desorption operations. When applied to simulated agricultural runoff, CPAC@Fe3O4 showcased a significant adsorption capacity of 160.71 mg/g for 50 mg/L 2,4-D, using a 0.2 g/L dosage at pH 2. This study showcased the transformation of copper pod biomass into a valuable magnetic nanoadsorbent capable of efficiently eliminating the noxious 2,4-D pollutant from aqueous environments.

Fabrication of FeSiBPCNbCu nanocrystalline soft magnetic powders with high saturation magnetization and low core loss

Fabrication of FeSiBPCNbCu nanocrystalline soft magnetic powders with high saturation magnetization and low core loss

Zn-Ti co-substituted LiZn microwave ferrites: Sintering characteristics and gyromagnetic properties

To meet the low-loss and high-frequency application requirements of modern electronic information systems for integrated microwave devices, Zn-Ti co-substituted LiZn microwave ferrites were prepared in this work. The results demonstrated that Zn-Ti co-substitution promoted the grain growth and densification process during sintering, leading to a decrease in the pore-induced linewidth (ΔHp) of LiZn composite microwave ferrites; the introduction of non-magnetic Zn2+ and Ti4+ ions lowered the content of Fe3+ ions in the ferrites, which reduced the magnetocrystalline anisotropy constant |K1| and thus diminished the anisotropy-induced linewidth (ΔHa). Besides, the dielectric loss of the material decreased with increasing Zn-Ti substitution amounts (x) due to the reduction of Fe2+ ion content. As a result, when x = 0.35, the FMR linewidth was decreased from ∼251 Oe to ∼97 Oe, and the dielectric loss was greatly reduced from >100×10−4 to ∼3.82×10−4 in the ferrites. The material also exhibited excellent properties including high saturation magnetization (∼3913 Gauss), high Curie temperature (∼304 °C), and low coercivity (∼2.05 Oe).

Effect of growth conditions on magnetization reversal and magnetic anisotropy in Co2Fe0.5Ti0.5Si quaternary Heusler alloy thin films

Ferromagnetic resonance and magneto-optic Kerr effect (MOKE) techniques are employed to unravel the nature of ‘in-plane’ (IP) magnetic anisotropy and magnetization reversal (MR) processes in magnetron-sputtered 100 nm Co2Fe0.5Ti0.5Si (CFTS) thin films, deposited (and subsequently annealed) at different substrate temperatures (Ts) ranging from 200 °C to 550 °C. By varying TS, the CFTS films are produced with different amounts of anti-site (AS) atomic disorder. Irrespective of the degree of AS disorder, the IP uniaxial magnetic anisotropy (UMA) is prevalent in all the CFTS films. The TS450 and TS500 films, deposited at T S = 450 °C and 500 °C, stand out as they have (i) the least AS disorder, (ii) lowest value (α = 0.0055) of the Gilbert damping constant, (iii) high saturation magnetization ( ≅770 G ) at 300 K, (iv) UMA energy density as high as ≅1.6×104erg/cc at 120 K dropping to ≅1.0×104erg/cc at 300 K, (v) spin-wave stiffness ( D ) at T = 0 K, D0≅175 meVÅ2 and, as in other CFTS films, the electron–magnon interaction is primarily responsible for the thermal renormalization of D . Furthermore, in the TS450 and TS500 films, MOKE hysteresis loops at various angles ( ψH ) that the field makes with the easy axis in the film plane, reveals two mutually exclusive UMAs, UMA1≫UMA2 , with easy axes perpendicular to each other. By contrast, only a single UMA is observed in all the remaining films. When ψH=0∘ , MOKE domain images reveal that, consistent with the uniaxial nature of magnetic anisotropy, an abrupt reversal of magnetization is accompanied by the formation of 180° domains. When ψH = 90°, due to the presence of two UMAs in TS450 and TS500 films, following the field reversal, first the reverse domains nucleate and then grow at the expense of the fundamental domains through field-induced domain wall motion.

Magnetic separation, sunlight-driven photocatalytic activity, and antibacterial studies of Sm-doped Co0.33Mg0.33Ni0.33Fe2O4 nanoparticles.

Magnetic nanoparticles have emerged as a promising tool for wastewater treatment due to their unique properties. In this regard, Co0.33Mg0.33Ni0.33SmxFe2-xO4 (0.00 x 0.08) nanoparticles were prepared to examine their magnetic separation efficiency (MSE), photocatalytic, antibacterial, and antibiofilm performances. Pure nanoparticles, having the highest saturation magnetization (Ms = 31.87emu/g), exhibit the highest MSE, where 95.6% of nanoparticles were separated after 20min of applying a magnetic field of 150 mT. The catalytic performance of the prepared samples is examined by the photodegradation of rhodamine B (RhB) dye exposed to direct sunlight radiation. Improved photocatalytic activity is exhibited by Co0.33Mg0.33Ni0.33Sm0.04Fe1.96O4 nanoparticles, labeled as Sm0.04, where the rate of the degradation reaction is enhanced by 4.1 times compared to pure nanoparticles. Rising the pH and reaction temperature improves the rate of the photodegradation reaction of RhB. The incorporation of 15 wt% reduced graphene oxide (rGO) with Sm0.04 enhanced the rate of the reaction by 1.7 and 2.4 times compared with pure Sm0.04 sample and rGO, respectively. The antibacterial and antibiofilm activities against Escherichia coli, Leclercia adecarboxylata, Staphylococcus aureus, and Enterococcus faecium are assessed by the minimum inhibitory concentration (MIC) and the minimum bactericidal concentration (MBC) broth microdilution, the agar well diffusion, the time-kill assays, the biofilm formation, and destruction assays. The bacteria used in these assessments are isolated from wastewater. The nanoparticles exhibit a bacteriostatic activity, with a better effect against the Gram-positive isolates. Co0.33Mg0.33Ni0.33SmxFe2O4 (x = 0.00) nanoparticles have the best effect. The effect is exerted after 2-3h of incubation. Gram-positive biofilms are more sensitive to nanoparticles.

Increasing the Particle Size and Magnetic Property of Iron Oxide Nanoparticles through a Segregated Nucleation and Growth Process.

Iron oxide nanoparticles (IONs) with good water dispersibility were prepared by the thermal decomposition of iron acetylacetonate (Fe(acac)3) in the high-boiling organic solvent polyethylene glycol (PEG) using polyethyleneimine (PEI) as a modifier. The nucleation and growth processes of the crystals were separated during the reaction process by batch additions of the reaction material, which could inhibit the nucleation but maintain the crystal growth, and products with larger particle sizes and high saturation magnetization were obtained. The method of batch addition of the reactant prepared IONs with the largest particle size and the highest saturation magnetization compared with IONs reported using PEG as the reaction solvent. The IONs prepared by this method also retained good water dispersibility. Therefore, these IONs are potentially suitable for the magnetic separation of cells, proteins, or nucleic acids when large magnetic responses are needed.

Turning Ultra-Low Coercivity and Ultra-High Temperature Stability Within 897 K via Continuous Crystal Ordering Fluctuations.

High-performance soft magnetic materials are important for energy conservation and emission reduction. One challenge is achieving a combination of reliable temperature stability, high resistivity, high Curie temperature, and high saturation magnetization in a single material, which often comes at the expense of intrinsic coercivity-a typical trade-off in the family of soft magnetic materials with homogeneous microstructures. Herein, a nanostructured FeCoNiSiAl complex concentrated alloy is developed through a hierarchical structure strategy. This alloy exhibits superior soft magnetic properties up to 897K, maintaining an ultra-low intrinsic coercivity (13.6 A m-1 at 297 K) over a wide temperature range, a high resistivity (138.08µΩcm-1 at 297K) and the saturation magnetization with only a 16.7% attenuation at 897 K. These unusual property combinations are attributed to the dual-magnetic-state nature with exchange softening due to continuous crystal ordering fluctuations at the atomic scale. By deliberately controlling the microstructure, the comprehensive performance of the alloy can be tuned and controlled. The research provides valuable guidance for the development of soft magnetic materials for high-temperature applications and expands the potential applications of related functional materials in the field of sustainable energy.

Flower-shaped magnetic fluorescent nanoparticles based lateral flow biosensor for highly sensitive detection of cardiac troponin I

Magnetic fluorescent nanoparticles have demonstrated notable advantages as multifunctional immunoassays in lateral flow biosensor (LFB), contributing to the enhancement of both the flexibility and practicability of LFB. Herein, we synthesized flower-shaped magnetic fluorescent Nanoparticles (FMNP@QDs) with heightened fluorescence emission. The distinctive core/shell architecture of FMNP@QDs comprised the high saturation magnetization core encapsulated by oleic acid-modified Fe3O4, the flower-shaped shell made up of polymer colloids, and quantum dots (QDs) uniformly distributed on the outside. After surface modified with PEG-COOH and conjugate with cardiac troponin I (cTnI) antibodies, the FMNP@QDs were successfully applied in LFB for highly sensitive cTnI detection in samples. The limit of detection (LOD) of the proposed LFB for cTnI was 0.0097 ng/mL under fluorescent mode and 0.026 ng/mL under magnetic mode. A high level of concordance was observed between the FMNP@QDs based fluorescent LFB and the commercial CLIA method. The results indicated that the FMNP@QDs based LFB has a substantial potential for point-of-care test (POCT) technology, owing to its simple operating procedures, affordability, and enhanced sensitivity.

A mesoporous magnetothermal nanopomegranate with acid-tolerant hierarchical structure for remote controlled drug delivery

Developing acid-tolerant magnetothermal nanoplatform with robust drug loading capacity for remote controlled drug release is challenging in the harsh acid environment of stomach. Herein, a nanopomegranate-type magnetothermal controllable drug release platform (FeCo@G@MSN), consisted of magnetothermal convertor (graphene-isolated FeCo nanocrystal core, FeCo@G) and drug reservoir (mesoporous silica, MSN), with acid-tolerant hierarchical structure was developed. Benefiting from the acid tolerance of graphene and MSN, FeCo@G@MSN was stable in 1 M hydrochloric acid for more than 12 h. The nanopomegranate-type hierarchical structure endowed FeCo@G@MSN with high saturation magnetization (114.9 emu/g) to generate a magnetothermal effect and large specific surface area (293.7 m2/g) to provide ample space for drug loading. As a proof of concept, a heat-triggered nitric oxide (NO) precursor was loaded, and NO were controlled released by breaking of S-NO bonds through localized heat derived from magnetothermal effect of FeCo@G, resulting in an inhibition effect towards Helicobacter pylori. A chemotherapeutic drug (doxorubicin, DOX) was also loaded and controlled released by breaking of hydrogen bonds between silica and DOX under remote an alternating magnetic field, thus exhibiting an inhibition effect towards gastric cancer cells. This work provides an efficient strategy to exploit magnetothermal controlled drug release platform and offers inspiration for the treatment of gastric diseases.

Extraction of gamma iron oxide (γ-Fe2O3) nanoparticles from waste can: Structure, morphology and magnetic properties

In this work, the transformation of waste iron cans to gamma iron oxide (γ-Fe2O3) nanoparticles following acid leaching precipitation method along with their structural, surface chemistry, and magnetic properties was studied. Highly magnetic iron-based nanomaterials, maghemite with high saturation magnetization have been synthesized through an acid leaching technique by carefully tuning of pH and calcination temperature. The phase composition and crystal structure, surface morphology, surface chemistry, and surface composition of the synthesized γ-Fe2O3 nanoparticles were explored by X-ray diffraction (XRD), Scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS) and Energy-dispersive X-ray spectroscopy (EDS). The XRD results confirm the cubic spinel structure having crystallite size 26.90–52.15 nm. The XPS study reveals the presence of Fe, O element and the binding energy of Fe (710.31 and 724.48 eV) confirms the formation of γ-Fe2O3 as well. By dynamic light scattering (DLS) method and zeta potential analyzer, the particle size distribution and stability of the systems were investigated. The magnetic behavior of the synthesized γ-Fe2O3 nanoparticles were studied using a vibrating sample magnetometer (VSM) which confirmed the ferrimagnetic particles with saturation magnetization of 54.94 emu/g. The resultant maghemite nanoparticles will be used in photocatalysts and humidity sensing. The net impact of the work stated here is based on the principle of converting waste into useful nanomaterials. Finally, it was concluded that our results can give insights into the design of the synthesis procedure from the precursor to the high-quality gamma iron oxide nanoparticles with high saturation magnetization for different potential applications which are inexpensive and very simple.

Preparation and study of the effect of pH value on structural, morphological, electrical and magnetic properties of CoFe2O4 nanoparticles prepared by sol-gel precipitation method

The present study reports the synthesis of cobalt ferrite nanoparticles (CoFe2O4 NPs) using the sol-gel precipitation process via mixing a stoichiometric ratio of cobalt chloride (1 M) and ferric chloride (2 M). The molar of ferric to cobalt was mentioned (2:1) and then 2 M of sodium hydroxide was added. The structural and morphological features of the material were assessed using X-ray diffraction (XRD), Scanning electron microscopy (SEM), and atomic force microscopy (AFM). The electrical properties were analyzed using an LCR meter, while the magnetic properties were measured using a vibrating sample magnetometer (VSM). Fourier-transform infrared spectroscopy (FTIR) investigated the material's molecular vibrations. The X-ray diffraction (XRD) analysis revealed that all the samples exhibited a cubic spinal structure, and no additional peak was detected. Interestingly, the average size of the crystallites (D) decreased from 17.74 nm to 16.58 nm as the pH level increased from 7 to 13. This finding provides important insights into the behaviour of the tested samples under different pH conditions. The formation of the ferrite spine was confirmed by FTIR spectroscopy, with the primary detected bands (408.92–470.65 cm−1) attributed to the octahedral complexes and (516.94–588.31 cm−1) assigned to the tetrahedral ones. The dielectric and imaginary part of the dielectric constant decreased with increasing pH values excluding samples prepared at pH = 11. All samples with different pH values exhibit resonance peaks at frequencies up to (1 KHz). The magnetic measurements carried out by the VSM instrument, the result show that the saturation magnetization increases with increasing pH and the higher saturation magnetization is 68 emu. g1.

Fabrication of an Fe-Doped ZIF-67 Derived Magnetic Fe/Co/C Composite for Effective Removal of Congo Red.

The dyes in printing and dyeing wastewater are harmful to the human body and the environment. It is essential to develop practical and effective adsorbents to deal with them. In this study, an Fe-doped, ZIF-67 derived Fe/Co/C composite material with strong magnetism was successfully synthesized. The effects of pH, initial concentration, and adsorption time on the properties of the adsorbent were investigated. To further improve the removal efficiency and enhance the practicality, potassium peroxymonosulfate (PMS) was added to the system due to its Fenton-like effect. Then, an Fe/Co/C composite was used with PMS to remove Congo red (CR) with a 98% removal of 250 mg·L-1. Moreover, for its high saturation magnetization of 85.4 emu·g-1, the Fe/Co/C composite can be easily recovered by applying a magnetic field, solving the problem that powdery functional materials are difficult to recover and, thus, avoiding secondary pollution. Furthermore, since the composite material was doped before carbonization, this synthetic strategy is flexible and the required metal elements can be added at will to achieve different purposes. This study demonstrates that this Fe-doped, ZIF-67 derived magnetic material has potential application prospects for dye adsorption.

Magnetic Field-Optimized Paramagnetic Nanoprobe for T2/T1 Switchable Histopathological-Level MRI.

Traditional magnetic resonance imaging (MRI) contrast agents (CAs) are a type of "always on" system that accelerates proton relaxation regardless of their enrichment region. This "always on" feature leads to a decrease in signal differences between lesions and normal tissues, hampering their applications in accurate and early diagnosis. Herein, we report a strategy to fabricate glutathione (GSH)-responsive one-dimensional (1-D) manganese oxide nanoparticles (MONPs) with improved T2 relaxivities and achieve effective T2/T1 switchable MRI imaging of tumors. Compared to traditional contrast agents with high saturation magnetization to enhance T2 relaxivities, 1-D MONPs with weak Ms effectively increase the inhomogeneity of the local magnetic field and exhibit obvious T2 contrast. The inhomogeneity of the local magnetic field of 1-D MONPs is highly dependent on their number of primary particles and surface roughness according to Landau-Lifshitz-Gilbert simulations and thus eventually determines their T2 relaxivities. Furthermore, the GSH responsiveness ensures 1-D MONPs with sensitive switching from the T2 to T1 mode in vitro and subcutaneous tumors to clearly delineate the boundary of glioma and metastasis margins, achieving precise histopathological-level MRI. This study provides a strategy to improve T2 relaxivity of magnetic nanoparticles and construct switchable MRI CAs, offering high tumor-to-normal tissue contrast signal for early and accurate diagnosis.

Magnetic properties and microstructure of Ce and Zr synergetic stabilizing Ti-lean SmFe12-based strip-casting flakes

Recently ThMn12-type samarium iron alloys have been promising materials for permanent magnets. Due to the high abundance and low cost, Ce as a possible stabilizer can be introduced into ThMn12-type alloys. The effect of Ce doping on the magnetic moment and phase stability in Ti-lean (Ce,Sm,Zr)(Fe,Co,Ti)12 compounds were predicted by the first-principles calculations. The CexSm0.8-xZr0.2(Fe0.8Co0.2)11.5Ti0.5 (x = 0–0.8) alloys with ThMn12 structure were produced by strip-casting into flakes by a wheel speed of 1.5 m/s and annealed at 1000 °C for 24 h. The Ce0.8Zr0.2(Fe0.8Co0.2)11.5Ti0.5 annealed flake shows a high saturation magnetization value of 13.6 kGs at room temperature. With the increase of Ce substitution in the annealed flakes, the content of α-(Fe,Co,Ti) phase decreases and the saturation magnetization increases. The 1:12 phase and the 1:9 phase have an orientation relationship that can be expressed as [0 0 –1]1:12//[100]1:9 and (020)1:12//(010)1:9. Besides, annealing process promotes the formation of 1:12 phase transformed from 1:9 phase. Coercivity is expected to be improved by obtaining uniform microstructure and suppressing the formation of soft α-(Fe,Co,Ti) phase in the ThMn12-based alloys.

GMI-based biosensor for the detection and quantification of doxorubicin anticancer drugs labeled to Fe3O4 superparamagnetic nanoparticles

We present the results of research on a Co-based giant magnetoimpedance (GMI) biosensor for Fe3O4-labelled doxorubicin (DOX) anticancer drugs. Co62Fe5Ni4Si15B14 ribbons were used as biosensing material for test solutions containing different concentrations of DOX. The plain ribbon, ribbon+Fe3O4 and ribbon+DOX2 samples exhibited low coercivity (Hc), high saturation magnetization (Ms) and low anisotropy (Hk). The GMI ratio (ΔZ/Z) increased from 33% to 38% with the increase of doxorubicin content in the ribbon. It was found that the ΔZ/Z ratio first increased rapidly up to a frequency of ∼2 MHz, and then decreased slowly as the frequency increased. While the magnetic field dependent ΔZ/Z has a single peak at 1 MHz, it has a double peak at 5 MHz. It was found that the peak height of ΔZ/Z in the ribbons with test solution of 20 ng/ml and 50 ng/ml increased by ∼3% and ∼6%, respectively, compared to the ribbon without test solution. Then the ΔZ/Z ratio decreased very rapidly with the increase of the applied external magnetic fields. The frequency-dependent GMI sensitivity (η) increased with increasing frequency and reached a maximum value at a critical frequency (∼1.6 MHz), after which it decreased. The detection sensitivity of the GMI biosensor (ξ) increased rapidly with increasing doxorubicin concentration up to ∼80 ng/ml and then remained almost unchanged. The results show that doxorubicin (DOX+Fe3O4), used as an anticancer drug, can be effectively detected even at low concentrations using the GMI based sensors fabricated in this study.

Synthesis, physico-chemical properties, and AC induction heating of polycaprolactone-coated bio-compatible Fe3O4 nanoparticles

Ex-situ functionalization of Fe3O4 nanoparticles, synthesized using a coprecipitation method, with bio-compatible polycaprolactone (PCL) polymer is reported in this study. The formation of the crystalline structure of Fe3O4 is confirmed from the X-ray diffraction patterns. The presence of the PCL polymer on the surface of the coated MNPs is confirmed using Fourier transform infrared and X-ray photoelectron spectroscopy techniques and thermogravimetric analysis. Scanning and transmission electron microscopy imaging studies reveal the nearly spherical morphology of the synthesized nanoparticles. Room temperature magnetization measurements show the superparamagnetic nature of the PCL coated nanoparticles with high saturation magnetizations varying from ∼61–66 emu/g. Further, the room temperature coercivity is found to be reduced by ∼78 % for the PCL coated nanoparticles, which is attributed to the lowering of the interparticle interactions upon surface functionalization. Magnetic fluid hyperthermia studies on the PCL coated nanoparticles dispersed in ∼1 wt% agar gel shows significant alternating magnetic field induced heating efficiency, with temperature rise in the vicinity of the hyperthermia limit (∼42 °C). The highest specific absorption rate is found to be ∼85.4 ± 3.9 W/gFe, indicating an intrinsic loss power of ∼0.62 nHm2kg−1, which is significantly higher than the previously reported values for PCL coated Fe3O4 MNPs. The field induced heating efficiency is found to be correlated with the saturation magnetization of the PCL coated nanoparticles. In vitro cytotoxicity studies on human breast cancer (MCF-7) cell lines confirm the superior bio-compatibility of the PCL coated Fe3O4 nanoparticles. Superior field induced heating efficiency, coupled with good bio-compatibility makes the PCL functionalized Fe3O4 nanoparticles a potential candidate for magnetic fluid hyperthermia.

Enhancing trimethoprim pollutant removal from wastewater using magnetic metal-organic framework encapsulated with poly (itaconic acid)-grafted crosslinked chitosan composite sponge: Optimization through Box-Behnken design and thermodynamics of adsorption parameters

Trimethoprim (TMP), an antibiotic contaminant, can be effectively removed from water by using the innovative magnetic metal-organic framework (MOF) composite sponge Fe3O4@Rh-MOF@PIC, which is shown in this study. The composite is made up of magnetite (Fe3O4) nanoparticles and a rhodium MOF embedded in a poly(itaconic acid) grafted chitosan matrix. The structure and characteristics of the synthesized material were confirmed by thorough characterization employing SEM, FTIR, XPS, XRD, and BET techniques. Notably, the composite shows a high magnetic saturation of 64emug-1, which makes magnetic separation easier, according to vibrating sample magnetometry. Moreover, BET analysis revealed that the Fe3O4@Rh-MOF@PIC sponge had an incredibly high surface area of 1236.48m2/g. Its outstanding efficacy was confirmed by batch adsorption tests, which produced a maximum adsorption capacity of 391.9mg/g for the elimination of TMP. Due to its high porosity, magnetic characteristics, and superior trimethoprim uptake, this magnetic MOF composite sponge is a promising adsorbent for effective removal of antibiotics from contaminated water sources. An adsorption energy of 24.5kJ/mol was found by batch investigations on the Fe3O4@Rh-MOF@PIC composite sponge for trimethoprim (TMP) adsorption. The fact that this value was up 8kJ/mol suggests that the main mechanism controlling TMP absorption onto the sponge adsorbent is chemisorption. Chemisorption requires creating strong chemical interactions between adsorbate and adsorbent surface groups, unlike weaker physisorption. The magnetic composite sponge exhibited strong removal capabilities and high adsorption capacities for the antibiotic pollutant. The Fe3O4@Rh-MOF@PIC composite sponge also showed magnetism, which allowed for easy magnetic separation after adsorption. Over the course of 6cycles, it showed outstanding reusability, and XRD confirmed that its composition was stable. The high surface area MOF's pore filling, hydrogen bonding, π-π stacking, and electrostatic interactions were the main trimethoprim adsorption mechanisms. This magnetic composite is feasible and effective for removing antibiotics from water because of its separability, reusability, and synergistic adsorption mechanisms via electrostatics, H-bonding, and π-interactions. The adsorption results were optimized using Box Behnken-design (BBD).

Fe3O4/CoFe2O4 core-shell nanoparticles with enhanced magnetic properties for hyperthermia application

Fe3O4/CoFe2O4 core/shell nanoparticles with varying shell thickness were fabricated by seed-mediated growth via thermal decomposition method. Ligand exchange process using poly(maleic anhydride-alt-1-octadecene) (PMAO) was performed to prepare the aqueous magnetic fluids from the as-synthesised nanoparticles. X-ray diffraction (XRD), transmission electron microscopy (TEM) and Quantum Design PPMS VersaLab were utilised to characterise morphological and magnetic properties of the sample. XRD results showed that all the particles were single phase with spinel structure and the average crystallite size in the range of 11–17 nm. All particles were spherical in TEM images with similar size compared to results calculated from XRD. Magnetic measurements were performed at different temperatures (50 − 300 K) at 30 kOe. The result showed that the saturation magnetisation (M s) and coercivity (H C) were significantly increased with the formation of hard magnetic shell with varying thickness. The dynamic light scattering (DLS) analysis presented a narrow distribution and zeta potential of −16 to −35 mV, indicating a good stability of the ferrofluids. The cytotoxicity of the FOC3/PMAO ferrofluid, which has the highest SAR value of 372.02 W g−1, was tested on Hep-G2 cell line at different concentrations from 10 to 100 μg ml−1. Less than 30% of the cell was inhibited, indicating that the FOC3/PMAO particles have low toxicity at these tested concentrations. Thus, these as-synthesised core/shell nanoparticles with uniform particle size, high saturation magnetisation, good stability and five-time increased specific absorption rate (SAR) compared to the Fe3O4 core nanoparticles are very promising in hyperthermia and magnetic resonance imaging (MRI) applications.

Tuning Surface, Phase, and Magnetization of Superparamagnetic Magnetite by Ionic Liquids: Single-Step Microwave-Assisted Synthesis.

Achieving colloidal and chemical stability in ferrofluids by surface modification requires multiple steps, including purification, ex situ modification steps, and operation at high temperatures. In this study, a single-step microwave-assisted methodology is developed for iron oxide nanoparticle (IONP) synthesis utilizing a series of imidazolium-based ionic liquids (ILs) with chloride, bis(trifluoromethylsulfonyl)imide, and pyrrolide anions as the reaction media, thus eliminating the use of volatile organics while enabling rapid synthesis at 80 °C as well as in situ surface functionalization. The characterized surface functionality, hydrodynamic particle size, magnetization, and colloidal stability of the IONPs demonstrate a strong dependence on the IL structure, ion coordination strength, reactivity, and hydrophilicity. The IONPs present primarily a magnetite (Fe3O4) phase with superparamagnetism with the highest saturation magnetization at 81 and 73 emu/g at 10 and 300 K, respectively. Depending on the IL coating, magnetization and exchange anisotropy decrease by 20 and 2-3 emu/g (at 35 wt % IL), respectively, but still represent the highest magnetization achieved for coated IONPs by a coprecipitation method. Further, the surface-functionalized superparamagnetic magnetite nanoparticles show good dispersibility and colloidal stability in water and dimethyl sulfoxide at 0.1 mg/mL concentration over the examined 3 month period. This study reports on the intermolecular and chemical interactions between the particle surface and the ILs under synthetic conditions as they relate to the magnetic and thermal properties of the resulting IONPs that are well suited for a variety of applications, including separation and catalysis.