Synthesis and electromagnetic properties of microwave absorbing material: Cox(Cu0.5Zn0.5)1−xFe2O4 (0 < x < 1) nanoparticles

Spinel ferrite Co_x(Cu_0.5Zn_0.5)_1−xFe₂O₄ over a compositional range 0 < x < 1 was prepared using a simple hydrothermal method. Particle sizes could be varied from 14 to 25 nm by changing the x value. X-ray diffraction results confirmed that all the as-prepared nanoparticles revealed typical spinel structure and transmission electron microscopy images showed that the particle size of the samples increased with increasing x value. The magnetic properties of the as-prepared Co_x(Cu_0.5Zn_0.5)_1−xFe₂O₄ nanoparticles have been systematically examined. The maximum saturation magnetization existed at the highest Co content (x = 1). The electromagnetic properties of all the samples have been measured by an Agilent network analyzer and the results showed that Co_0.1(Cu_0.5Zn_0.5)_0.9Fe₂O₄ possessed the best microwave absorbing properties.     

Synthesis of Co3O4 nanoparticles via the CTAB-assisted method

Cobalt oxide (Co₃O₄) nanoparticles were successfully synthesized by the cetyltrimethylammonium bromide (CTAB)-assisted method at normal pressure for the first time. The structure and morphology of the as-prepared Co₃O₄ nanoparticles were characterized by powder X-ray diffracton (XRD), infrared spectroscopy (IR), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and N₂-sorption analysis. XRD studies indicated that the as-prepared product was well-crystallized cubic phase of Co₃O₄ with a cell constant of α = 8.0722 Å. The EM images showed that the obtained Co₃O₄ sample consisted of dispersive quasi-spherical particles with the size ranged from 15 to 25 nm.     

Magnetic softness and interparticle exchange interactions of (Fe65Co35)1 − x(Al2O3)x (x = 0-0.50) nanogranular films

The effect of Al₂O₃ content on the structure, electrical properties, magnetic properties, and interparticle exchange interactions of (Fe₆₅Co₃₅)_1 − x(Al₂O₃)_x films with Al₂O₃ volume fractions x ranging from 0 to 0.50 was systematically investigated. Among the films with x between 0 and 0.25, the lowest coercivity of 0.56 kA/m was achieved in the (Fe₆₅Co₃₅)_0.82(Al₂O₃)_0.18 film. This is ascribed to the strongest exchange interactions between the Fe₆₅Co₃₅ nanoparticles in this film. Combined with the microstructure analysis of the (Fe₆₅Co₃₅)_1 − x(Al₂O₃)_x films, the modified Herzer's model was extended to interpret the variation of the coercivity with x and analyze the effect of the exchange interactions between the Fe₆₅Co₃₅ nanoparticles on the magnetic softness. The remanence curves confirm the existence of the exchange interactions and reveal the evolution of the exchange interaction strength with Al₂O₃ content.     

Structural and magnetic properties of Mn nanoparticles prepared by arc-discharge

Mn nanoparticles are prepared by arc discharge technique. MnO, α-Mn, β-Mn, and γ-Mn are detected by X-ray diffraction, while the presence of Mn₃O₄ and MnO₂ is revealed by X-ray photoelectron spectroscopy. Transmission electron microscopy observations show that most of the Mn nanoparticles have irregular shapes, rough surfaces and a shell/core structure, with sizes ranging from several nanometers to 80 nm. The magnetic properties of the Mn nanoparticles are investigated between 2 and 350 K at magnetic fields up to 5 T. A magnetic transition occurring near 43 K is attributed to the formation of the ferrimagnetic Mn₃O₄. The coercivity of the Mn nanoparticles, arising mainly from Mn₃O₄, decreases linearly with increasing temperature below 40 K. Below the blocking temperature T_B ≈ 34 K, the hysteresis loops exhibit large coercivity (up to 500 kA/m), owing to finite size effects, and irreversibility in the loops is found up to 4 T, and magnetization is not saturated up to 5 T. The relationship between structure and the magnetic properties are discussed.     

One-step synthesis of Co–Ni ferrite/graphene nanocomposites with controllable magnetic and electrical properties

Co_1−xNi_xFe₂O₄/graphene nanocomposites were synthesized through a one-step solvothermal method. The as-synthesized products were characterized by X-ray powder diffraction, field emission scanning microscopy, transmission electron microscope, and high-resolution transmission electron microscope. The results show that the Co_1−xNi_xFe₂O₄ nanoparticles are uniformly dispersed on graphene sheets. The dependence of structure, magnetic and electrical properties of Co_1−xNi_xFe₂O₄/graphene nanocomposites on the Ni²⁺ concentration and the graphene content were also studied. The saturation magnetization and electrical conductivity of the as-prepared products reached 51.82 emu/g and 1.00 × 10² S/m, respectively.     

Temperature dependence of magnetic property and photocatalytic activity of Fe3O4/hydroxyapatite nanoparticles

Fe₃O₄/hydroxyapatite (HAP) nanoparticles have been developed as a novel photocatalyst support, based on the embedment of magnetic Fe₃O₄ particles into HAP shell via homogeneous precipitation method. The resultant nanoparticles were characterized by transmission electron microscope (TEM) and X-ray diffraction (XRD). These particles were almost spherical in shape, rather monodisperse and have a unique size of about 25 nm in diameter. The effect of calcination temperature on magnetic property and photocatalytic activity of Fe₃O₄/HAP nanoparticles was investigated in detail. The obtained results showed that the Fe₃O₄/HAP nanoparticles calcined at 400 °C possessed good magnetism and photocatalytic activity in comparison with that calcined at other temperatures.     

High frequency magnetic mechanism of Ni-substituted Co2Z hexagonal ferrite

The magnetic properties, especially the high frequency magnetic mechanism, of Ni-substituted Co₂Z hexagonal ferrite were studied. The polycrystalline Z-type hexagonal ferrite of Ba₃Ni_xCo_2−xFe₂₄O₄₁ (0 ≤ x ≤ 2) were prepared by solid-state reaction. The results indicate that Ni-substituted Co₂Z samples all exhibit typical soft magnetic character. Substitution of Ni for Co will turn the planar magnetocrystalline anisotropy of Co₂Z to uniaxial anisotropy when x ≥ 1, so that the permeability drops dramatically and domain wall resonance appears in the frequency spectra. With the rise of Ni amount or sintering temperature, domain wall resonance strengthens gradually.     

Surface engineered magnetic nanoparticles for removal of toxic metal ions and bacterial pathogens

Surface engineered magnetic nanoparticles (Fe₃O₄) were synthesized by facile soft-chemical approaches. XRD and TEM analyses reveal the formation of single-phase Fe₃O₄ inverse spinel nanostructures. The functionalization of Fe₃O₄ nanoparticles with carboxyl (succinic acid), amine (ethylenediamine) and thiol (2,3-dimercaptosuccinic acid) were evident from FTIR spectra, elemental analysis and zeta-potential measurements. From TEM micrographs, it has been observed that nanoparticles of average sizes about 10 and 6 nm are formed in carboxyl and thiol functionalized Fe₃O₄, respectively. However, each amine functionalized Fe₃O₄ is of size ∼40 nm comprising numerous nanoparticles of average diameter 6 nm. These nanoparticles show superparamagnetic behavior at room temperature with strong field dependent magnetic responsivity. We have explored the efficiency of these nanoparticles for removal of toxic metal ions (Cr³⁺, Co²⁺, Ni²⁺, Cu²⁺, Cd²⁺, Pb²⁺ and As³⁺) and bacterial pathogens (Escherichia coli) from water. Depending upon the surface functionality (COOH, NH₂ or SH), magnetic nanoadsorbents capture metal ions either by forming chelate complexes or ion exchange process or electrostatic interaction. It has been observed that the capture efficiency of bacteria is strongly dependent on the concentration of nanoadsorbents and their inoculation time. Furthermore, these nanoadsorbents can be used as highly efficient separable and reusable materials for removal of toxic metal ions.     

Synthesis and characterization of spinel Co3O4 octahedra enclosed by the {1 1 1} facets

Spinel Co₃O₄ octahedra synthesized by a facile redox-precipitation method were investigated for the complete oxidation of methane. XRD analysis showed that the spinel structural Co₃O₄ octahedra had a relatively strong (1 1 1) diffraction peak as compared with that of the irregular shaped Co₃O₄ nanoparticles prepared by a conventional precipitation method. The results of methane combustion test demonstrated that the Co₃O₄ octahedra had no catalytic activity at 300-500 °C, while the Co₃O₄ irregular nanoparticles were highly active at the same reaction conditions. HRTEM studies revealed that the Co₃O₄ octahedra were predominantly exposed by the low Miller-index {1 1 1} facets with the lowest surface energy, and the Co₃O₄ irregular nanoparticles were exposed by various crystal facets. The results exhibited that the {1 1 1} facets with the low surface energy of the Co₃O₄ octahedra resulted in the inert catalytic activity in the methane oxidation reaction.     

Characterization and magnetic properties of Sm- and Gd-substituted CoFe2O4 nanoparticles prepared by forced hydrolysis in polyol

Pure nanoparticles of the CoFe_2−xRE_xO₄ (RE = Gd, Sm; x = 0.0, 0.1) system have been prepared by forced hydrolysis in polyol. The insertion of Sm³⁺ and Gd³⁺ cations into the cobalt ferrite structure has been investigated. X-ray micro-analysis (EDX) shows that the RE contents are close to the nominal ones. X-ray diffraction (XRD) evidences a cell size increase with slight distortions in the spinel-like lattice indicating the entrance of RE³⁺ ions. Micro-Raman spectroscopy confirms the cubic inverse-spinel structure and rules out the existence of impurities like hematite. Magnetic measurements (SQUID) show important differences in the magnetic properties of the unsubstituted and substituted particles. All the particles are superparamagnetic at room temperature and ferrimagnetic at low temperature. However, their main magnetic characteristics appear to be directly dependent on the RE content.     

Shape controlled synthesis of iron-cobalt alloy magnetic nanoparticles using soft template method

Fe_xCo_1 − x alloy nanoparticles of spherical (x = 0.25, 0.68, 0.85), hollow spherical (x = 0.60) and sheet like (x = 0.60) shapes were prepared at room temperature by reduction of iron chloride tetrahydrate and cobalt chloride hexahydrate with sodium borohydride, using N-Cetyl-N,N,N-trimethyl ammonium bromide (CTAB)/water/hexanol system as soft template. The size and shapes of nanostructures were found to depend on the concentrations of CTAB and hexanol in water. Composition and shape dependence of magnetic properties of spherical, hollow spherical and sheet like Fe_xCo_1 − x alloy nanostructures were discussed. The highest saturation magnetization of 235 emu/g with a coercivity of 160 Oe was obtained for spherical Fe_0.68Co_0.32 nanoparticles.     

Hydrothermal fabrication of various morphological α-Fe2O3 nanoparticles modified by surfactants

Two kinds of various morphological α-Fe₂O₃ nanoparticles modified by anionic surfactant (sodium dodecylsulfonate, SDS) and cationic surfactant (hexadecyipyridinium chloride, HPC), respectively, have been synthesized via hydrothermal method, using simple inorganic salt (NH₄)₃Fe(C₂O₄)₃ and alkali NaOH as starting precursors. Meanwhile, α-Fe₂O₃ nanoparticles without surfactant are also fabricated under the same conditions for comparison. The resultant products were characterized by means of Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), transmission electron micrograph (TEM) combined with electron diffraction (ED) and magnetization measurements. It is interesting that the obtained α-Fe₂O₃ nanoparticles without surfactant are polyhedral with average particle size of 90 ± 35 nm; while the obtained α-Fe₂O₃ nanoparticles modified by SDS are ellipsoidal with mean particle size of major axis: ca. 420 nm; minor axis: ca. 205 nm and those modified by HPC are spherical with mean particle size of ca. 185 nm observed from TEM. In addition, magnetic hysteresis measurements reveal that the α-Fe₂O₃ nanoparticles modified by two surfactants show enhancement in coercivity (H_c) and the remanent magnetization (M_r) compared with those of the obtained α-Fe₂O₃ nanoparticles without surfactant at room temperature. The experimental results suggest that the surfactants not only significantly influence the size and shape of the particles, but also their magnetic properties.     

Preparation and properties of nickel ferrite (NiFe2O4) nanoparticles via sol-gel auto-combustion method

Using nickel and ferric nitrates and citric acid, NiFe₂O₄ nanoparticles are prepared by a simple and cost-effective polyvinylpyrrolidone (PVP) assisted sol-gel auto-combustion method. The synthesised nanoparticles consist of single phase inverse spinel structure of NiFe₂O₄. The particles are in spherical shape with an average size of ∼8 nm. The vibrational properties show tetrahedral and octahedral sites of NiFe₂O₄ nanoparticles. The super-paramagnetism is observed with magnetic saturation (M_s) of 50.4 emug^−1.     

Hydrothermal synthesis and magnetic properties of Co0.2Cu0.03Fe2.77O4 nanoparticles

Co_0.2Cu_0.03Fe_2.77O₄ nanoparticles with different morphologies have been synthesized directly via a simple hydrothermal method. The effects of pH value, precursor concentration, reaction temperature and surfactant on the particle size were discussed. X-ray diffraction analyses showed that the as-synthesized Co_0.2Cu_0.03Fe_2.77O₄ nanoparticles possessed typical spinel structure. Scanning electron microscope images showed different morphologies of the particles, including truncated octahedron and octahedron. It was indicated that well-dispersed Co_0.2Cu_0.03Fe_2.77O₄ nanoparticles can be synthesized at pH values ranging from 11 to 13, and reaction temperature of 160 °C. The particle size decreased from 18 to 10 nm after the addition of sodium dodecyl sulphate at the pH value of 9. The magnetic measurement showed that the as-prepared Co-Cu spinel ferrite nanoparticles possessed hard magnetic property.     

Preparation of Fe3O4/PVA nanofibers via combining in-situ composite with electrospinning

A novel approach, combining in-situ composite method with electrospinning, was used to prepare high magnetic Fe₃O₄/poly(vinyl alcohol) (PVA) composite nanofibers. Fe₃O₄ magnetic fluids were synthesized by chemical co-precipitation method in the presence of 6 wt.% PVA aqueous solution. PVA was used as stabilizer and polymeric matrix. The resulting Fe₃O₄/PVA composite nanofibers were characterized with field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM) and X-ray diffractometer (XRD), respectively. These composite fibers showed a uniform and continuous morphology, with the Fe₃O₄ nanoparticles embedded in the fibers. Magnetization test confirmed that the composite fiber showed a high saturated magnetization (M_s = 2.42 emµ·g^-1) although only 4 wt.% content.     

Synthesis, characterization and magnetic properties of nanocrystalline Ni-Zn-Co ferrites

Nanocrystalline magnetic particles of Ni_0.7−xZn_0.3Co_xFe₂O₄ with x lying between 0.0 and 0.3 were synthesized by combustion method using metal nitrates, sucrose and polyvinyl alcohol (PVA). The synthesized powders where characterized by X-ray diffraction and Transmission electron microscopy (TEM). The average crystallite size determined from XRD data using Scherrer formula lie in the range of 20-30 nm. TEM micrographs show a well defined nano-crystallite state with an average particle size of around ~ 10 nm. The electron diffraction patterns confirm the spinel crystal structure of the ferrite. Magnetic properties measured at room temperature by vibrating sample magnetometer (VSM) reveal an increase in saturation magnetization with increase in cobalt concentration. Non-linear increase in saturation magnetization is related to surface effects and method of preparation.     

Preparation of polybenzoxazine-functionalized Fe3O4 nanoparticles through in situ Diels–Alder polymerization for high performance magnetic polybenzoxazine/Fe3O4 nanocomposites

Hybrids and nanocomposites of polymer and magnetic Fe₃O₄ nanoparticles have been utilized as magnetically-responsive materials and magnetically-directed nanoparticles. In this work, we prepare polymer-functionalized Fe₃O₄ nanoparticles through in situ Diels–Alder polymerization using maleimide-functionalized Fe₃O₄ nanoparticle as a precursor. Polybenzoxazine-functionalized Fe₃O₄ nanoparticles (MNP-PBz) have been obtained and characterized with Fourier Transform Infrared, X ray photoelectron, and Raman spectroscopies. The high saturation magnetization value of 51.9 emu g⁻¹ of the MNP-PBz nanoparticles demonstrates its superparamagnetism. Moreover, MNP-FBz has been utilized as a nanofiller for preparation of cured PBz/MNP-PBz nanocomposites, which contain various MNP-PBz contents of 67, 50, 33, and 17 wt.%. The sample of PBz/MNP-PBz-67 shows a storage modulus of 8.0 GPa, a saturation magnetization value of 37.6 emu g⁻¹, and a glass transition temperature above 380 °C. As a result, the PBz/MNP-PBz nanocomposites could be classified as magnetically-responsive high performance materials.     

Synthesis and magnetic behavior of spinel FeAl2O4 nanoparticles

Nanocrystalline FeAl₂O₄ has been synthesized from furnace heating of corresponding iron and aluminium acetylacetonate complexes. The nanoparticles obtained were characterized using powder X-ray diffraction (XRD), EDX and transmission electron microscopy (TEM). The particles were faceted with a diameter in the range of 10-20 nm. The magnetic property of the FeAl₂O₄ nanoparticles was studied for the first time by plotting M vs H hysteresis curves, at different temperature and also by recording the temperature dependence of zero-field-cooled M_ZFC and field-cooled M_FC magnetization curves. On decreasing the temperature to 4 K, the magnetization shows deviation from linear behavior.     

Synthesis of single-phase Sr3Co2Fe24O41 Z-type ferrite by polymerizable complex method

Synthesis of single-phase Sr₃Co₂Fe₂₄O₄₁ Z-type (Sr₃Co₂Z) ferrite was realized by adopting the polymerizable complex method. Crystal structure of samples has been investigated by powder X-ray diffraction (XRD). Single-phase Sr₃Co₂Z ferrite was obtained by heating at 1473 K for 5 h in air. Magnetic properties were discussed by measurements of M-H curves with vibrating sample magnetometer (VSM). Sr₃Co₂Z ferrite prepared by polymerizable complex method showed typical M-H curve of soft ferrite, with a saturation magnetization of 21.5μ_B/formula unit (50.5 emu/g) and a coercive force of 0.014 T at room temperature.     

Structural and magnetic properties of glass-ceramics containing silver and iron oxide

Glass-ceramics with a nominal composition of 25SiO₂–(50 − x)CaO–15P₂O₅–8Fe₂O₃–2ZnO–xAg (where x = 0, 2 and 4 mol%) have been prepared. Structural features of glass-ceramics have been investigated using X-ray diffraction (XRD) and scanning electron microscope (SEM) techniques. Magnetic properties were studied using vibrating sample magnetometer and Mössbauer spectroscopy. Ca₃(PO₄)₂, hematite and magnetite are formed as major crystalline phases. The microstructure reveals the formation of 25–30 nm size particles. Mössbauer spectroscopy has shown the relaxation of magnetic particles. Saturation magnetization value is increased with an increase of Ag content up to 4 mol%, which has been attributed to the formation of magnetically ordered particles. The antibacterial response was found to depend on Ag ions concentration in the glass matrix and samples with 4 mol% Ag in glass matrix have shown effective antibacterial activity against Escherichia coli.