Magnetic Thermocouples Made of Co–Fe and Ni–Fe Permalloys

Technical Physics - Magnetized and unmagnetized Co–Fe and Ni–Fe alloys fabricated on a two-high casting installation in the form of thin flexible amorphous films are promising materials...     

Phonon- and phason-dynamics in Al–Cu–Fe quasicrystals

The lattice dynamics of quasicrystals includes local phason jumps as well as phonons. Phason dynamics is important for the understanding of both the structure and atomic motion in quasicrystals, leading to short-ranged atomic motion not involving vacancies in addition to diffusion. We have studied the phason and phonon dynamics of icosahedral i-Al₆₂Cu_25.5Fe_12.5. Quasielastic Mössbauer spectroscopy (QMS) was used to probe the iron phason dynamics. Inelastic nuclear-resonant absorption (INA) of synchrotron radiation and inelastic neutron scattering (INS) were used to study the iron-partial as well as the total vibrational DOS (VDOS). We find from preliminary QMS studies that iron atoms jump on a time scale about two orders of magnitude slower than that found for copper. The EFG shows an abrupt change in slope at ca. 825 K which may be related to a transition from simple (isolated) to more complicated (co-operative) phason jumps. From INA we find that the iron-partial VDOS differs radically from that of the total (neutron-weighted) generalised VDOS measured by INS. Both these properties are related to the specific local environments of Fe and Cu in i-AlCuFe.     

Magnetic properties of spray-formed Fe–6.5%Si and Fe–6.5%Si–1.0%Al after rolling and heat treatment

The maximum silicon content in commercial Fe–Si steels is limited to about 3.5 wt%Si, since the ductility declines sharply as this maximum is exceeded, hindering the production of thin sheets by cold/hot rolling. However, the best magnetic properties are attained at about 6.5 wt%Si, a silicon content that renders magnetostriction practically null and minimizes magnetic losses. Using spray-forming, our research group has successfully produced this type of high silicon alloy in thin sheet form by carefully controlling the many variables of the process and subsequent rolling operations. In the present study, we investigated the magnetic properties and the microstructure of spray-formed Fe–6.5 wt%Si and Fe–6.5 wt%Si–1.0 wt%Al alloys after warm rolling and heat treatment. The main cause for the brittleness of Fe–6.5 wt%Si alloy has been attributed to the B2 phase long-range ordering, which leads to premature fractures. The presence of aluminum could avoid B2 formation and improve the alloy's ductility. The binary Fe–6.5 wt% Si alloy showed the best magnetic properties, which were ascribed to a recrystallized, coarse grain size (∼500 μm; and 340 μm for the Al-containing alloy). TEM analysis showed that a well-developed B2 domain structure (about 50–300 nm in size) was formed in the binary alloy when low cooling rates are prevailing after heat treatment. This structure contributed to improve additionally the magnetic properties, but its effect was not so strong as that of the grain size. The addition of Al to the binary alloy suppressed B2 formation, as indicated by Mossbauer spectroscopy, and apparently hindered excessive grain growth, which may explain the slightly poorer magnetic properties when compared with the binary alloy.     

Precipitation and fracture behaviour of Fe–Mn–Ni–Al alloys

The effects of Al addition on the precipitation and fracture behaviour of Fe–Mn–Ni alloys were investigated. With the increasing of Al concentration, the matrix and grain boundary precipitates changed from L1₀ θ-MnNi to B2 Ni₂MnAl phase, which is coherent and in cube-to-cube orientation relationship with the α′-matrix. Due to the suppression of the θ-MnNi precipitates at prior austenite grain boundaries (PAGBs), the fracture mode changed from intergranular to transgranular cleavage fracture. Further addition of Al resulted in the discontinuous growth of Ni₂MnAl precipitates in the alloy containing 4.2?wt.% Al and fracture occurred by void growth and coalescence, i.e. by ductile dimple rupture. The transition of the fracture behaviour of the Fe–Mn–Ni–Al alloys is discussed in relation to the conversion of the precipitates and their discontinuous precipitation behaviour at PAGBs.     

The structure and composition of novel electrodeposited Sn–Fe and Sn–Co–Fe alloys from a flow circulation cell system

This study involved the use of a flow circulation cell, using varying circulation rates as a room temperature process (20°C). Mössbauer and XRD analysis were conducted to ascertain whether amorphous or microcrystalline structures could be obtained at 20°C using a range of current densities. Amorphous or microcrystalline structures of Sn–Fe and Sn–Co–Fe have potentially important industrial applications for energy efficient cells, for use as high performance electrodes in lithium batteries, as environmentally acceptable corrosion resistant materials and are derived from an energy efficient environmentally friendly electrolyte process which would be acceptable as an industrial process. $^{\it 57}Fe$ and $^{\it 119}Sn$ Mössbauer investigations supported by XRD analysis confirmed that the room temperature flow circulation cell gave rise to previously unknown non-equilibrium amorphous structures which do not occur in the corresponding thermally prepared alloys as shown in the thermal equilibrium diagrams. Mössbauer analysis shows these alloys to be both amorphous and ferromagnetic. It is shown that the flow circulation cell used at 20°C based on the environmentally friendly gluconate bath reported gives amorphous based Sn–Fe and Sn–Co–Fe alloys over a useful range of current densities facilitated by using a range of circulation rates.     

Interdiffusion and solid solution strengthening in Ni–Co–Pt and Ni–Co–Fe ternary systems

Diffusion couple experiments are conducted in Co–Ni–Pt system at 1200?°C and in Co–Ni–Fe system at 1150?°C, by coupling binary alloys with the third element. Uphill diffusion is observed for both Co and Ni in Pt rich corner of the Co–Ni–Pt system, whereas in the Co–Ni–Fe system, it is observed for Co. Main and cross interdiffusion coefficients are calculated at the composition of intersection of two independent diffusion profiles. In both the systems, the main interdiffusion coefficients are positive over the whole composition range and the cross interdiffusion coefficients show both positive and negative values at different regions. Hardness measured by performing the nanoindentations on diffusion couples of both the systems shows the higher values at intermediate compositions.     

Microstructure investigations and magnetic after-effect in amorphous and nanocrystalline Fe–Zr–Ti–B–Cu alloy

The microstructure evolution and low field magnetic properties i.e. initial magnetic susceptibility, stabilization field and magnetic after-effect as disaccommodation of the amorphous and nanocrystalline Fe₈₀Zr₄Ti₃B₁₂Cu₁ alloy were investigated. The heat treatment of the as-quenched Fe₈₀Zr₄Ti₃B₁₂Cu₁ alloy at 773 K for 1 h leads to its nanocrystallization. It was stated that initial magnetic susceptibility increases and intensity of disaccommodation decreases with increasing of annealing temperature. The magnetic after-effect of the investigated nanocrystalline samples is connected with relaxation processes that occur in the amorphous matrix.     

ICEMS study of isothermal oxidation of Fe–Mn–Al–C–Cr–Si–Mo, Fe–Mn–Al–C–Cr–Si and Fe–9Cr–1Mo alloys

The purpose of this paper is to investigate the isothermal behavior of Fe–27.3Mn–7.6Al–C–6.5Cr–0.25Si–0.88Mo (Mo(0)) and Fe–27.3Mn–7.6Al–1.0C–6.5Cr–0.25Si (Mo(1)) alloys and compare it against Fe–9Cr–1Mo (FCR) commercial alloy. The experiments were carried out at 600°C, 700°C, 750°C and 850°C, each one during 72 h in static air. The oxidation kinetics was measured as a function of time using a Thermogravimetry analyzer (TGA). The structure and composition of the oxide scale were characterized by X-ray diffraction (XRD) and Integral Conversion Electron Mössbauer Spectroscopy (CEMS). The TGA results show that at all oxidation temperatures the sample FCR exhibit the lowest kinetic corrosion and the lowest weight gain, whereas Mo(0) the highest. By CEMS technique it were found a broad magnetic sextet, which has been fit by one hyperfine field distribution with mean hyperfine field characteristic to ferritic/martensite phase, one Fe^3?+? doublet and one singlet for the Mo(0) and Mo(1) alloys. Samples oxidized at highest temperatures exhibit a strong paramagnetic line, probably due that the Cr or Mn oxides may be enriched on the surface. Then, the magnetic phase can be converted partially into austenite phase at highest temperatures.     

Magnetic properties and reduction characteristics of Fe–Co–B catalysts

Hyperfine Interactions - The effect of the amount of boron on the magnetic properties and the reduction characteristics of Fe–Co–B catalysts have been studied by Thermal Programmed...     

Anomalous microstructure and magnetocaloric properties in off-stoichiometric La–Fe–Si and its hydride

In the present work we reported the phase formation, microstructure, magnetocaloric effect and hydrogenation behavior of La-rich La1.7Fe11.6Si1.4alloy. In this off-stoichiometric La(Fe,Si)13alloy, the Na Zn13-type La(Fe,Si)13matrix phase shows faceted grains, with the Cr5B3-type La5Si3 used as the secondary phase distributed intergranularly. Such a peculiar morphology quickly forms upon one day annealing. In La1.7Fe11.6Si1.4alloy, we have observed a significant field dependence of magnetostructural transition temperature(～ 6.3 K/T), resulting in a large and table-like entropy change(△S～ 18 J/kg·K in 2 T) over a broad temperature range(～ 10 K). Upon hydrogenation, the maximum value of △S keeps almost unchanged, while the Curie temperature increases up to 350 K. These results indicate that the investigated offstoichiometric La(Fe,Si)13alloy is a promising magnetic material for magnetic refrigerators.     

Magnetic and Resonant Properties of Fe–Bi Films

Physics of the Solid State - Film structures in the Fe–Bi system have been studied experimentally. The magnetic state of the two-layer structures is shown by electron magnetic resonance to be...     

Phase constitution and microstructure of Ce–Fe–B strip-casting alloy

The strip-casting technique plays an important role in fabricating high coercivity sintered magnet. In this paper, we investigate the phase constitution and the microstructure of rapidly solidified Ce-Fe-B alloy fabricated by strip-casting. We find that the Ce2FelgB phase coexists with Fe, Fe2B, and CeFe2 phases in the Ce-Fe-B strips. The eutectic stucture consisting of Fe and Fe2B is encased in Ce2Fe14B grains, which is blocked by the CeFe2 grains at triple junctions, indicating that the microstructure of Ce-Fe-B strip is characteristic of a peritectic solidification. Thermal analysis indicates that the large supercooling of Ce2Fe14B results in the residual Fe and Fe2B. The microstructural optimization in Ce-Fe-B strips without Fe and Fe2B could be achieved by a heat treatment of 1000 ℃.     

Formation and crystallization kinetics of Nd–Fe–B-based bulk amorphous alloy

In order to improve the glass-forming ability (GFA) of Nd–Fe–B ternary alloys to obtain fully amorphous bulk Nd–Fe–B-based alloy, the effects of Mo and Y doping on GFA of the alloys were investigated. It was found that the substitution of Mo for Fe and Y for Nd enhanced the GFA of the Nd–Y–Fe–Mo–B alloys. It was also revealed that the GFA of the samples was optimized by 4 at.% Mo doping and increased with the Y content. The fully amorphous structures were all formed in the Nd $_{6-{x}}$ Y $_{{x}}$ Fe $_{68}$ Mo $_{4}$ B $_{22}$ (x $=$ 1–5) alloy rods with 1.5 mm-diameter. After subsequent crystallization, the devitrified Nd $_{3}$ Y $_{3}$ Fe $_{68}$ Mo $_{4}$ B $_{22}$ alloy rod exhibited a uniform distribution of grains with a coercivity of 364.1 kA/m. The crystallization behavior of Nd $_{3}$ Y $_{3}$ Fe $_{68}$ Mo $_{4}$ B $_{22}$ BMG was investigated in isothermal situation. The Avrami exponent n determined by JAM plot is lower than 2.5, implying that the crystallization is mainly governed by a growth of particles with decreasing nucleation rate.     

Studying the properties of Fe and Fe–Co nanotubes in polymer ion-track membranes

Iron and iron–cobalt nanostructures are probed by means of Mössbauer spectroscopy combined with scanning electron microscopy, energy-dispersion analysis, and X-ray diffraction. The obtained nanostructures are single-phase Fe_{1 ? x}Co _x (0 ≤ x ≤ 1) nanotubes that have high degrees of polycrystallinity and a bcc lattice 12 μm long and 110 ± 3 nm in diameter, with walls 21 ± 2 nm thick. A random distribution of the orientations of the magnetic momenta of Fe atoms are observed for Fe nanotubes, while Fe–Co nanotubes are characterized by a magnetic texture along their axes.     

Synthesis and Stabilization of Fe–Nd–B Nanoparticles for Biomedical Applications

Stable composition of Iron Neodymium Boron nanoparticles are formed by a chemical method. Conventional borohydride reduction method was used. The particles are in the size range of 30–100 nm. Silica coating was applied to stabilize and prepare the particles for in vitro applications such as cell separation and diagnostics. Morphology of particles has been studied along with the structure and magnetic properties.     

Preparation and magnetic properties of Fe–Ag granular alloy

An aqueous solution of AgNO₃ in the presence of ammonia and Fe(CO)₅ is sonicated under a H₂/Ar mixture, yielding a nanostructured homogeneous phase of Ag/Fe₂O₃. This composite material is further reduced at 300°C under hydrogen to produce the nanophased Fe/Ag solid mixture. The as-prepared material, as well as the reduced mixture, is analyzed by various conventional methods. Magnetization loops, ESR, Mössbauer, and magnetoresistance measurements are also conducted to determine the magnetic properties of the products.     

Structural and magnetic properties of Fe–Ni mecanosynthesized alloys

Fe_100???x Ni _x samples with x?=?22.5, 30.0 and 40.0 at.% Ni were prepared by mechanical alloying (MA) with milling times of 10, 24, 48 and 72 h, a ball mass to powder mass (BM/PM) ratio of 20:1 and rotation velocity of 280 rev/min. Then the samples were sintered at 1,000°C and characterized by X-ray diffraction (XRD) and transmission Mössbauer spectrometry (TMS). From the refinement of the X ray patterns we found in this composition range two crystalline phases, one body centered cubic (BCC), one face centered cubic (FCC) and some samples show FeO and Fe₃O₄ phases. The obtained grain size of the samples shows their nanostructured character. Mössbauer spectra were fitted using a model with two hyperfine magnetic field distributions (HMFDs), and a narrow singlet. One hyperfine field distribution corresponds to the ferromagnetic BCC grains, the other to the ferromagnetic FCC grains (Taenite), and the narrow singlet to the paramagnetic FCC grains (antitaenite). Some samples shows a paramagnetic doublet which corresponds to FeO and two sextets corresponding to the ferrimagnetic Fe₃O₄ phase. In this fit model we used a texture correction in order to take into account the interaction between the particles with flake shape and the Mössbauer $\upgamma$ -rays.     

Synthesis and Reactivity of Mg(II)–Fe(II)–Fe(III) Hydroxycarbonates

Green rust-like compounds (GRs) were discovered as natural minerals in various hydromorphic soils, where anoxic conditions allow their stability. They may control some redox processes in aquifers and participate to the transformation of various pollutants. Since Mg(II) cations are present in the fields where GRs were discovered, a partial substitution of Mg(II) to Fe(II) leading to intermediate compounds between GRs and usual Mg(II)–Fe(III) hydroxysalts is suspected. Mg(II)–Fe(II)–Fe(II) hydroxycarbonates can be obtained as intermediate oxidation products of (Mg, Fe)(OH)₂ in carbonate-containing aqueous media obeying to [Fe^II _4(1–x)Mg^II _4x Fe^III ₂(OH)₁₂]²⁺ [CO₃ ^2– nH₂O]^–2. TMS spectra at 12 K are similar to those of GRs, i.e., two quadrupole doublets, one due to Fe(II) with a large isomer shift =1.29 mms^–1 (with respect to -iron at room temperature) and quadrupole splitting E _Q=2.76 mms^–1, the other one due to Fe(III) with smaller hyperfine parameters =0.49 mms^–1 and E _Q=0.44 mms^–1. Fe(II) ions oxidise rapidly into Fe(III) with dissolved O₂. The reactivity is similar to that of Fe(II)–Fe(III) hydroxysalts GR, and thus the potential of Mg(II)–Fe(II)–Fe(III) compounds for reducing pollutants.