Fabrication of magnetic nickel–tungsten–phosphorus particles by electroless deposition

Nickel–tungsten–phosphorus (NiWP) particles with diameters ranging from 100 to 300 nm were fabricated by electroless deposition on silica particles and Au seeds. TEM, SEM equipped with EDX, and SQUID were employed to characterize these particles. It is found that 70 °C is sufficient to deposit NiWP particles, in contrast to 90 °C required for NiP or NiWP deposited on planar substrates. Magnetic properties of these particles are profoundly influenced by P-contents, whereas replacement of P with W changes the particles from paramagnetic to soft-ferromagnetic nature. Curie temperatures and saturation magnetization of these particles are around 300 K and from 0.1 to 20 emu/g, respectively.     

Production of magnetic microspheres by ultrasonic atomisation

Magnetic microspheres, with mean particle sizes from 23 to 32 μm were produced by the ultrasonic atomisation of a suspension of magnetite particles, of approximately 200 nm diameter, in a solution of poly–l–lactic acid (PLLA). The mean particle diameter and the width of the particle diameter distribution both increased with increasing magnetite concentration. The particles appear to be suitable for magnetic hyperthermic treatment of liver cancers, with the hysteresis loop areas increasing linearly with nominal magnetite concentration up to 30 wt% magnetite.     

Magnetic nanoparticles as building blocks for high-performance magnetic materials

We report on the magnetic behaviour of films of Fe nanoparticles deposited from the gas phase with sizes in the range 2–3 nm embedded in Ag and Co matrices and Co nanoparticles of the same size embedded in Ag matrices. Magnetometry measurements, using a VSM, of very low volume fraction (1–2%) assemblies of Fe and Co in Ag show perfect superparamagnetism and enable us to confirm that the size distribution of the particles in the matrix is the same as that of the free particles prior to deposition. The hysteresis loops at 2 K, which is below the blocking temperature, show that the particles have a uniaxial anisotropy that is randomly oriented in three dimensions with the Co nanoparticles having a much higher anisotropy than the Fe particles. The soft magnetic behaviour of pure Fe and Co nanoparticle films with no matrix is well described by a random anisotropy model and is consistent with the formation of a correlated super-spin glass (CSSG) characteristic of amorphous materials. The Co nanoparticle films appear to have a lower random anisotropy than the Fe ones in contrast to the behaviour observed for the isolated particles. Films of Fe nanoparticles embedded in Co matrices, whose saturation magnetization exceeds the Slater–Pauling curve, also show magnetic behaviour consistent with a CSSG. At high volume fractions, the films of Fe nanoparticles embedded in Co matrices behave almost identically to films of pure Co nanoparticles.     

Synthesis and rheological investigation of a magnetic fluid using olivary silica-coated iron particles as a precursor

A new type of magnetic fluid was prepared by dispersing monodispersed iron–silica (Fe–SiO₂) composite particles in polyethylene glycol (PEG) 400. The composite particles Fe–SiO₂ were synthesized by hydrogen reduction from α-Fe₂O₃–SiO₂ spheres. Their microstructures were observed by a high-resolution transmission electron microscope (HRTEM) and the magnetism was characterized with a superconducting quantum interference device (SQUID) magnetometer. Both steady-state and dynamic rheological properties of the magnetic fluid under different magnetic fields were studied by using a rheometer. Experimental results show that this magnetic fluid has a relatively high magnetoviscous effect at low shear rates. The yield stress of this material shows an increasing trend with a magnetic flux density. Also, viscoealstic properties of such materials are different from conventional ones.     

Influence of dextran coating on the magnetic behaviour of iron oxide nanoparticles

Magnetic iron oxide nanoparticles with mean diameters in the range from 10 to 30 nm were prepared by modified chemical precipitation routes. The particles were suspended in an aqueous solution by coating of the particles with carboxymethyldextran. A stability against agglomeration was achieved over a period of more than 7 days. In the present investigation, the structural and the magnetic properties of the nanoparticles were investigated. The influence of the dextran shell on the strength of the dipole–dipole interactions between the neighbouring particles was determined by investigation of the remanence behaviour (Henkel plot) of coated as well as of uncoated particles.     

Synthesis and magnetic properties of cobalt ferrite (CoFe2O4) nanoparticles prepared by wet chemical route

Magnetic nanoparticles of cobalt ferrite have been synthesized by wet chemical method using stable ferric and cobalt salts with oleic acid as the surfactant. X-ray Diffraction (XRD) and Transmission Electron Microscope (TEM) confirmed the formation of single-phase cobalt ferrite nanoparticles in the range 15–48 nm depending on the annealing temperature and time. The size of the particles increases with annealing temperature and time while the coercivity goes through a maximum, peaking at around 28 nm. A very large coercivity (10.5 kOe) is observed on cooling down to 77 K while typical blocking effects are observed below about 260 K. The high field moment is observed to be small for smaller particles and approaches the bulk value for large particles.     

Preparation of the SrFe12O19-based magnetic composites via boron oxide glass devitrification

Magnetic composites were obtained in the system SrO–Fe₂O₃–B₂O₃ by oxide glass heat treatment at 600–950 °C. Samples of the composites were investigated using XRD analysis, magnetic measurements, electron microcopy, and thermal analysis. It was shown that chemical composition of the precursor oxide glass and thermal treatment conditions influenced on the SrFe₁₂O₁₉ particles morphology and magnetic properties. The composites and powders were obtained containing hexaferrite as single domain platelet crystals or polycrystalline aggregates with a coercive force up to 6300 Oe in the former case and 4200 Oe in the latter case.     

Nanostructural,magnetic and electrical properties of Ag doped Mn-ferrite nanoparticles

Nano-crystalline MnFe_2−xAg_xO₄ (x = 0, 0.1, 0.2, 0.3 and 0.6) samples with average grain size of 4–7 nm were synthesized by a simple method based on decomposition of metal nitrates in presence of citric acid. The samples were characterized by different structural, magnetic and electrical measurements. Rietveld refinement of X-ray diffraction data confirmed cubic spinel structure of the samples. Results show that Ag doping decreases the crystallite size, magnetization and coercivity of nanoparticles. By increasing the Ag content in the samples the saturation magnetization shows interesting temperature dependent behavior. It was realized that magnetization of smaller particles show higher sensitivity to temperature variations than larger particles. DC electrical resistivity measurements in the temperature range of 300–650 K show that the resistivity first increases and then decreases by increasing the Ag content in the samples. Curie temperature (T_c) and polaron activation energy in ferromagnetic and paramagnetic regions were estimated by using resistivity curves.     

Ni–Zn–Sm nanopowder ferrites: Morphological aspects and magnetic properties

Ni–Zn ferrites have been widely used in components for high-frequency range applications due to their high electrical resistivity, mechanical strength and chemical stability. Ni–Zn ferrite nanopowders doped with samarium with a nominal composition of Ni_0.5Zn_0.5Fe_2−xSm_xO₄ (x=0.0, 0.05, and 0.1 mol) were obtained by combustion synthesis using nitrates and urea as fuel. The morphological aspects of Ni–Zn–Sm ferrite nanopowders were investigated by X-ray diffraction, nitrogen adsorption by BET, sedimentation, scanning electron microscopy and magnetic properties. The results indicated that the Ni–Zn–Sm ferrite nanopowders were composed of soft agglomerates of nanoparticles with a high surface area (55.8–64.8 m²/g), smaller particles (18–20 nm) and nanocrystallite size particles. The addition of samarium resulted in a reduction of all the magnetic parameters evaluated, namely saturation magnetization (24–40 emu/g), remanent magnetization (2.2–3.5 emu/g) and coercive force (99.3–83.3 Oe).     

In vitro study of magnetic particle seeding for implant assisted-magnetic drug targeting

The concept of using magnetic particles (seeds) as the implant for implant assisted-magnetic drug targeting (IA-MDT) was analyzed in vitro. Since this MDT system is being explored for use in capillaries, a highly porous (ε∼70%), highly tortuous, cylindrical, polyethylene polymer was prepared to mimic capillary tissue, and the seeds (magnetite nanoparticles) were already fixed within. The well-dispersed seeds were used to enhance the capture of 0.87 μm diameter magnetic drug carrier particles (MDCPs) (polydivinylbenzene embedded with 24.8 wt% magnetite) under flow conditions typically found in capillary networks. The effects of the fluid velocity (0.015–0.15 cm/s), magnetic field strength (0.0–250 mT), porous polymer magnetite content (0–7 wt%) and MDCP concentration (C=5 and 50 mg/L) on the capture efficiency (CE) of the MDCPs were studied. In all cases, when the magnetic field was applied, compared to when it was not, large increases in CE resulted; the CE increased even further when the magnetite seeds were present. The CE increased with increases in the magnetic field strength, porous polymer magnetite content and MDCP concentration. It decreased only with increases in the fluid velocity. Large magnetic field strengths were not necessary to induce MDCP capture by the seeds. A few hundred mT was sufficient. Overall, this first in vitro study of the magnetic seeding concept for IA-MDT was very encouraging, because it proved that magnetic particle seeds could serve as an effective implant for MDT systems, especially under conditions found in capillaries.     

Abnormal reduction of coercivity on magnetic cobalt–platinum alloy films

Ultrathin Co–Pt alloy films as substrate were studied by the surface magneto-optical Kerr effect. As the growth of Ni, the films show uniquely high polar Kerr responses without any in-plane signals. The coercivity decreased until the thickness of Ni film was higher than 5 ML. A new surface structure was discovered at 7–10 ML Ni/Co–Pt films by the low-energy electron diffraction. Interestingly, polar Kerr signal and coercivity of the 10 ML Ni/Co–Pt(1 1 1) template film reduced rapidly as Co films were further deposited onto only about 1–2 ML. Then the films show a canted magnetization with a rollback hysteresis in the polar configuration during the growth of Co. Coercivity of the 7 ML Co/Ni/Co–Pt film was found unusually down to almost 100 Oe.The corresponding magic number at around 7 ML of Co in the abnormal reduction of coercivity may be attributed to the cluster formations of Co.     

New magnetic organic–inorganic composites based on hydrotalcite-like anionic clays for drug delivery

The structural “memory effect” of anionic clays was used to obtain layered double hydroxides (LDHs) with tailored magnetic properties, by loading iron oxides and/or spinel structures on iron partially substituted hydrotalcite-like materials. The obtained magnetic layered structures were further used as precursors for new hybrid nanostructures, such as aspirin–hydrotalcite-like anionic clays. Transmission electron microscopy (TEM) analysis shows that small iron oxide or spinel nanoparticles coexist with the fibrous drug particles on the surface of partially aggregated typical clay-like particles. The specific saturation magnetization of the loaded LDHs can be increased up to 70 emu/g by using specific post-synthesis treatments.     

In situ hybridization to chitosan/magnetite nanocomposite induced by the magnetic field

Chitosan/magnetite nanocomposite was synthesized induced by magnetic field via in situ hybridization in ambient condition. Results of XRD patterns and TEM micrographs indicated that magnetite particles with 10–20 nm were dispersed in chitosan homogeneously. An interesting result is that magnetite nanoparticles were assembled to form chain-like structures under the influence of the external magnetic field, which mimics the magnetite chains inside of magnetotatic bacteria. The saturated magnetization (Ms) of nano-magnetite in chitosan was 50.54 emu/g, which is as high as 54% of bulk magnetite. The remanence (Mr) and coercivity (Hc) were 4 emu/g and14.8 Oe, respectively, which indicated that magnetite nanoparticles were superparamagnetic. The key of route is that a pre-precipitated chitosan hydrogel membrane, used as chemical reactor, which controlled the precipitation of chitosan precipitation and in situ transformation of magnetite from the precursor simultaneously in the magnetic field environment.     

Ferromagnetic seeding for the magnetic targeting of drugs and radiation in capillary beds

A new implant assisted-magnetic drug targeting approach is introduced and theoretically analyzed to demonstrate its feasibility. This approach uses ferromagnetic particles as seeds for collecting magnetic drug carrier particles at the desired site in the body, such as in a capillary bed near a tumor. Based on the capture cross section (λ_c) approach, a parametric study was carried out using a 2-D mathematical model to reveal the effects of the magnetic field strength (μ₀H₀=0.01–1.0 T), magnetic drug carrier particle radius (R_p=20–500 nm), magnetic drug carrier particle ferromagnetic material content (x_fm,p=20–80 wt%), average blood velocity (u_B=0.05–1.0 cm/s), seed radius (R_s=100–2000 nm), number of seeds (N_s=1–8), seed separation (h=0–8R_s), and magnetic drug carrier particle and seed ferromagnetic material saturation magnetizations (iron, SS 409, magnetite, and SS 304) on the performance of the system. Increasing the magnetic field strength, magnetic drug carrier particle size, seed size, magnetic drug carrier particle ferromagnetic material content, or magnetic drug carrier particle or seed saturation magnetization, all positively and significantly affected λ_c, while increasing the average blood velocity adversely affected it. Increasing the number of seeds or decreasing the seed separation, with both causing less significant increases in λ_c, verified that cooperative magnetic effects exist between the seeds that enhance the performance. Overall, these theoretical results were encouraging as they showed the viability of this minimally invasive, implant assisted-magnetic drug targeting approach for targeting drugs or radiation in capillary beds.     

Black Cr/α-Cr2O3 nanoparticles based solar absorbers

Monodisperse spherical core–shell particles of Cr/α-Cr₂O₃ with high adhesion were successfully coated on rough copper substrates by a simple self-assembly-like method for the use in solar thermal absorbers. The structure and morphology of the core-shell particles of Cr/α-Cr₂O₃ were effectively controlled by deposition temperature and the pH of the initial precursor solution. Their characterizations were carried out with X-ray diffraction, scanning electron microscopy, energy dispersive spectrometry and attenuated total reflection, as well as UV–vis diffuse reflectance spectroscopy. The samples aged for more than 40 h at 75 °C exhibit the targeted high absorbing optical characteristic “Black chrome” while those aged for ≤40 h show a significant high UV–vis diffuse reflectance “green color”.     

Suitability of water based magnetic fluid with CoFe2O4 particles in hyperthermia

Magnetic susceptibility of the magnetic fluid with CoFe₂O₄ particles was measured in the low-frequency range in order to determine mean values of the magnetic grain size and the saturation magnetisation. The volume concentration of the solid phase (CoFe₂O₄) was also found. Results of the calorimetric measurements, in the range from 70 kHz to 1.7 MHz, confirmed the suitability of use of the medium studied in magnetic fluid hyperthermia, especially in the frequency region 600–800 kHz. The H²–law-type dependence of the specific absorption rate on the square amplitude of the magnetic field testified to the presence of superparamagnetic particles in the magnetic fluid. The minimum magnetic field intensity needed for successful hyperthermal treatment was experimentally determined.     

Preparation,surface modification and microwave characterization of magnetic iron fibers

In this paper, magnetic iron fibers of 3–10 μm diameter and an adjustable aspect ratio were synthesized successfully by a method involving pyrolysis of carbonyl under a magnetic field. A surface modification technology was also investigated. The electromagnetic parameters of the iron-fiber–wax composites were measured using the transmission/reflection coaxial line method in the microwave frequency range of 2–18 GHz. The results show that the prepared iron-fiber–wax composites exhibit high magnetic loss that can be further improved after phosphating. On the other hand, the complex permittivity was significantly decreased after phosphating. As a result, this kind of iron fiber may be useful for thin and lightweight radar-absorbing materials.     

Structural and magnetic characterization of soft-magnetic FeCo alloy nanoparticles

Soft-magnetic FeCo alloy nanoparticles with diameters less than 100 nm are prepared by ball milling. X-ray photoemission spectroscopy (XPS) and X-ray magnetic circular dichroism (XMCD) are used to characterize these particles. While the XPS spectrum from the as-prepared sample clearly shows Co photoemission peaks, no sign of Fe is observed in the same spectrum. However, Fe photoemission peaks appear after 1 h of Ar ion sputtering. A quantitative analysis of the XPS spectra shows an increase of Fe concentration versus sputtering time until the Fe:Co ratio of the bulk alloy is reached. In addition, the narrow scan Fe and Co 2p XPS spectra show that Co is more oxidized than Fe. All these measurements indicate that the nanoparticles have a Co shell and an Fe-rich core. They further demonstrate the usefulness of XPS combined with depth-profiling via sputtering to obtain element- and chemically-sensitive structural information on nanoparticles. XMCD as an element-specific magnetic analysis tool further reveals that Fe and Co are ferromagnetically coupled in these particles. The information obtained is useful for establishing a structure–property relation for the studied material that is expected to have applications as a soft magnetic material at high temperatures.     

Magnetization reversal of ferromagnetic nanoparticles under inhomogeneous magnetic field

We investigated remagnetization processes in ferromagnetic nanoparticles under inhomogeneous magnetic field induced by the tip of magnetic force microscope (MFM) in both theoretical and empirical ways. Systematic MFM observations were carried out on arrays of submicron-sized elliptical ferromagnetic particles of Co and FeCr with different sizes and periods. It clearly reveals the distribution of remanent magnetization and processes of local remagnetization of individual ferromagnetic particles. Modeling of remagnetization processes in ferromagnetic nanoparticles under magnetic field induced by MFM probe was performed on the base of Landau–Lifshitz–Gilbert equation for magnetization. MFM-induced inhomogeneous magnetic field is very effective to control the magnetic state of individual ferromagnetic nanoparticles as well as to create different distribution of magnetic field in array of ferromagnetic nanoparticles.     

Sm–Co films for high-density magnetic recording media

In this experiment, Cr–Cu thin film was used as an underlayer for Sm–Co film. The magnetic properties and crystal structure of Sm–Co films prepared onto this kind of underlayer have been studied. Grain size and surface roughness have been reduced with the introduce of Cr. The Cr addition into the Cu underlayer also improves the c-axis orientation of Sm–Co films. As a result, films with squareness ratio as high as 0.95 and perpendicular coercivity as high as 12.3 kOe have been prepared.