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The new cast steel with a chemical composition of Fe-(0.85-0.95)C-(1.50-1.60)Si-(2.40-2.60)Mn-(1.0-1.2)Al-(0.30-0.40)­Mo-(0.10-0.15)V-(1.0-1.1)Ni (all in wt.%) was investigated in aspect of formation of the multiphase microstructure leading to high strength and ductility. Two types of heat treatment technologies were developed. The first one involves softening annealing at a temperature of 650°C for 4 hours, heating up to 950°C and holding for 2 hours, and then fast cooling down to 200°C and isothermally treated for 2 hours. The second one involves homogenizing annealing at 1100°C for 6 hours, then cooling with furnace down to 950°C and holding for 2 hours, then fast cooling down to 200°C and isothermally treated for 2 hours. A unique microstructure of cast steel consisting of martensite and retained austenite plates of various thicknesses and volume fractions was obtained. Additionally, nanometric transition carbides were noticed after the above-mentioned heat treatments. This microstructure ensures high hardness, strength and plasticity ( Rm = 1426 MPa and A = 9.5%), respectively, due to the fact that TWIP/TRIP processes occur during deformation related to the high volume fraction of retained austenite, which the stacking fault energy is above 15 mJ/m –2 resulting from the chemical composition of the investigated cast steel.

In the present paper, we present an electron magnetic resonance (EMR) study of Ni50.2Mn28.3Ga21.5 powders obtained from melt-spun ribbons in the milling process. We registered EMR spectra in various temperatures at the X-band. In the EMR spectra recorded for the samples taken at the beginning of the milling process, the “training effect” was observed. After 2 h of milling, this phenomenon was no longer observed. To determine the basic EMR parameters, such as linewidth, resonance field, and asymmetry parameters, the experimental data were fitted using a single metallic Lorentz line. In high-temperature regions, we observed the influence of dispersion on the shape of the spectra, but as the temperature decreased, the asymmetry of line was reduced. The shift in the resonance field value at high temperatures and the temperature dependence of the linewidth below Curie temperature indicate that the investigated samples exhibited a characteristics of a spin-glass alloy.

Shape memory alloys (SMAs) represent an exceptional class of smart materials as they are able to recover their shape after mechanical deformation, making them suitable for use in actuators, sensors and smart devices. These unique properties are due to the thermoelastic martensitic transformation that can occur during both thermal and mechanical deformation. Cu-based SMAs, especially those incorporating Al and Ag, are attracting much attention due to their facile production and cost-effectiveness. Among them, Cu-Al-Ag SMAs stand out due to their notably high temperature range for martensitic transformation. In this study, a Cu-based SMA with a new ternary composition of Cu-10Al-7Ag wt.% was prepared by arc melting and the samples cut from this casting alloy were quenched in water. Subsequently, the phase composition and the development of the microstructure were investigated. In addition, the morphology of the martensite was studied using advanced techniques such as electron backscatter diffraction (EBSD) and transmission electron microscopy (TEM). The analyzes confirmed the presence of martensitic structures in both samples; mainly 18R (β1′) martensite was present but a small volume fraction of (γ1′) martensite also was noticed in the as-quenched sample. The observation of fine, twinned martensite plates in the SMA alloy with symmetrically occurring basal plane traces between the twin variants underlines the inherent correlation between microstructural symmetry and the properties of the material and provides valuable insights into its behavior. The hardness of the quenched sample was found to be lower than the as-cast counterpart, which can be linked to the solutioning of Ag particles during the heat treatment.

This study presents research results concerning the vacuum carburizing of four steel grades, specifically conforming to European standards 1.7243, 1.6587, 1.5920, and 1.3532. The experimental specimens exhibited variations primarily in nickel content, ranging from 0 to approximately 3.8 wt. %. As a comparative reference, gas carburizing was also conducted on the 1.3532 grade, which had the highest nickel content. Comprehensive structural analysis was carried out on the resultant carburized layers using a variety of techniques, such as optical and electron scanning, transmission microscopy, and X-ray diffraction. Additionally, mechanical properties such as hardness and fatigue strength were assessed. Fatigue strength evaluation was performed on un-notched samples having a circular cross-section with a diameter of 12 mm. Testing was executed via a three-point bending setup subjected to sinusoidally varying stresses ranging from 0 to maximum stress levels. The carburized layers produced had effective thicknesses from approximately 0.8 to 1.4 mm, surface hardness levels in the range of 600 to 700 HV, and estimated retained austenite contents from 10 to 20 vol%. The observed fatigue strength values for the layers varied within the range from 1000 to 1350 MPa. It was found that changing the processing method from gas carburizing, which induced internal oxidation phenomena, to vacuum carburizing improved the fatigue properties to a greater extent than increasing the nickel content of the steel.

AlSi11 matrix composites reinforced with SiC particles have been fabricated by high pressure die casting assisted by ultrasonic mixing. Severe plastic deformation process was performed on the as cast AlSi/2wt.%SiC composite using the modified channel with the twisted output (TCAP) at three temperatures of 350, 400 and 450 °C. The TCAP tool consists of helical part in the horizontal area of the channel allowing for simulation of back pressure and thus resulted in the increase of extrusion force and local plastic deformation. The most important issue of the presented investigations was to refine dendritic cast microstructure of the prepared composite during one pass of TCAP. As a result, a composite with a matrix containing equiaxed α(Al) grains of few microns depending on TCAP temperature and β(Si) particles of about 1 μm in size with twinned structure was produced. The dynamic recrystallization process during TCAP at 450 °C manifested by the grain growth of α(Al) and decrease of dislocation density was observed to affect the sample hardness causing its decrease. The mechanical properties of the composite extruded by TCAP were measured by compression testes and the maximum plastic deformation of about 35% and the compressive strength near 300 MPa were observed. These values were similar for all samples extruded at temperatures between 350 and 450 °C and generally are better comparing with AK11 alloy subjected to different plastic deformation processes.

Al matrix nanocomposites reinforced with TiC particles have been successfully fabricated by self-propagating high-temperature reaction during casting from aluminium 1000 alloy and a mixture of powders of Ti, C and Al used as a moderator. The most important issue was to estimate the influence of moderator content on the microstructure. The microstructure of composites containing a lower amount of moderator (1% and 10%) consists of TiC particles, segregated mainly at grain boundaries of aluminium matrix, while a higher moderator content (>50%) allows to obtain materials with nearly homogenous distribution of TiC particles. Moreover, the elimination of brittle, additional phases e.g. TiAl3 and Al4C3, commonly observed in the Al/TiC composites, was evidenced. However, still small amounts of Ti3AlC and TiAl2.4Si0.6 phases that reduce the capacity of TiC were identified. The composites exhibit improved mechanical properties with regard to aluminium base alloy. The highest value of the relative increase of yield strength was found in the composite with 50% of moderator due to relatively small TiC particle size, well separated and uniformly distributed in the matrix.

This work describes the production of nanocrystalline TiO2 and SnO2 oxides, as well as their nanocomposites (containing 26.9, 58.7 and 79.0 wt.% of SnO2) with two-stage sol-gel method combined with high temperature treatment. The phase composition and medium size crystallites were determined using X-ray diffraction analysis (XRD) and revealed that the nanocomposites crystallize in tetragonal structures of TiO2 - anatase and SnO2 - cassiterite. Specific surface area of the nanopowders, measured using sorption method (BET), changed from 42.1 to 160.8 m2/g. The morphology of the nanopowders was observed using transmission electron microscope (TEM). As indicated by TEM images, the manufactured nanopowders were well crystallized and consisted of small, spherical grains. The obtained nanopowders were also tested for NH3 gas detection application. The presented method of nanopowders synthesis enables to obtain nanocrystalline TiO2 and SnO2 oxides, as well as composites from TiO2-SnO2 of known and controlled chemical and phase composition. It also enables to obtain composites used for gas sensors. The sensor made of composite containing 58.7 wt.% of SnO2 exhibited the best NH3 sensing features.

In this work, based on the thermodynamic prediction, the comprehensive studies of the influence of Cu for Fe substitution on the crystal structure and magnetic properties of the rapidly quenched Fe85B15 alloy in the ribbon form are performed. Using thermodynamic calculations, the parabolic shape dependence of the ΔGamoprh with a minimum value at 0.6% of Cu was predicted. The ΔGamoprh from the Cu content dependence shape is also asymmetric, and, for Cu = 0% and Cu = 1.5%, the same ΔGamoprh value is observed. The heat treatment optimization process of all alloys showed that the least lossy (with a minimum value of core power losses) is the nanocomposite state of nanocrystals immersed in an amorphous matrix obtained by annealing in the temperature range of 300–330 °C for 20 min. The minimum value of core power losses P10/50 (core power losses at 1T@50Hz) of optimally annealed Fe85-xCuxB15 x = 0,0.6,1.2% alloys come from completely different crystallization states of nanocomposite materials, but it strongly correlates with Cu content and, thus, a number of nucleation sites. The TEM observations showed that, for the Cu-free alloy, the least lossy crystal structure is related to 2–3 nm short-ordered clusters; for the Cu = 0.6% alloy, only the limited value of several α-Fe nanograins are found, while for the Cu-rich alloy with Cu = 1.2%, the average diameter of nanograins is about 26 nm, and they are randomly distributed in the amorphous matrix. The only high number of nucleation sites in the Cu = 1.2% alloy allows for a sufficient level of grains’ coarsening of the α-Fe phase that strongly enhances the ferromagnetic exchange between the α-Fe nanocrystals, which is clearly seen with the increasing value of saturation induction up to 1.7T. The air-annealing process tested on studied alloys for optimal annealing conditions proves the possibility of its use for this type of material.

We present a study of the annealing effect and its influence on magnetic and structural properties for a series of Heusler alloys Ni50−xCoxMn35.5In14.5 (x=0,3,5) prepared in ribbon form. We studied the morphology and composition using scanning electron microscopy (SEM) equipped with an X-ray microanalyzer (EDX). The magnetic properties were determined by two methods: electron magnetic resonance (EMR) and vibrating sample magetometer (VSM). We found that cobalt content in the annealed samples reveals an additional magnetic phase transition at lower temperatures.

In the present work, we investigated in detail the thermal/crystallization behavior and magnetic properties of materials with Fe84.5-xCoxNb5B8.5P2 (x = 0, 5, 10, 15 and 20 at.%) composition. The amorphous ribbons were manufactured on a semi-industrial scale by the melt-spinning technique. The subsequent nanocrystallization processes were carried out under different conditions (with/without magnetic field). The comprehensive studies have been carried out using differential scanning calorimetry, X-ray diffractometry, transmission electron microscopy, hysteresis loop analyses, vibrating sample magnetometry and Mössbauer spectroscopy. Moreover, the frequency (up to 300 kHz) dependence of power losses and permeability at a magnetic induction up to 0.9 T was investigated. On the basis of some of the results obtained, we calculated the values of the activation energies and the induced magnetic anisotropies. The X-ray diffraction results confirm the surface crystallization effect previously observed for phosphorous-containing alloys. The in situ microscopic observations of crystallization describe this process in detail in accordance with the calorimetry results. Furthermore, the effect of Co content on the phase composition and the influence of annealing in an external magnetic field on magnetic properties, including the orientation of the magnetic spins, have been studied using various magnetic techniques. Finally, nanocrystalline Fe64.5Co20Nb5B8.5P2 cores were prepared after transverse thermo-magnetic heat treatment and installed in industrially available portable heating equipment.

The paper describes the process of TiO2-SnO2 nanocomposites manufacturing utilizing two-step sol-gel method combined with calcination (in the case of titanium hydroxide gel) or hydrothermal treatment (in the case of tin hydroxide). Phase composition of the obtained nanopowders and average crystallite sizes were determined using XRD analysis. Measurements of the specific surface area were performed using sorption method based on determination of physical adsorption isotherm (BET). Morphology of the nanopowders was observed using transmission electron microscope. The presented synthesis method enables to obtain composites nanopowders from TiO2-SnO2 system with known and controlled chemical and phase compositions, and distinctly diversified TiO2 and SnO2 particle sizes.

Selective Laser Melting was successfully used as a fabrication method to produce Ni-Mn-Ga and Ni-Mn-Ga-Fe ferromagnetic shape memory alloys. The starting material in a powder form with an average particle size of about 17.6 µm was produced by milling of as melt-spun ribbons. The microstructure, phase composition, and martensitic transformation behavior of both powder precursors and laser melted alloys were investigated by several methods, including high energy X-ray diffraction, electron microscopy, and vibrating sample magnetometry. The as laser melted materials are chemically homogenous and show a typical layered microstructure. Both alloy compositions have a duplex structure consisting either of austenite and 10M martensite (Ni-Mn-Ga) or a mixture of 14M and NM martensitic phases (Ni-Mn-Ga-Fe), contrary to the as milled powder precursors showing fcc structure in both cases. The forward martensitic transformation takes place at 336 and 325 K for Ni-Mn-Ga and Ni-Mn-Ga-Fe, respectively, while the magnetic response is much stronger for Ni-Mn-Ga than for the quaternary alloy. The results show that Selective Laser Melting allows for producing of good quality, homogenous materials. However, their microstructural features and consequently shape memory behavior should be tailored by additional heat treatment.

The effect of substitution of Fe by Cu on the crystal structure and magnetic properties of Fe72−xNi8Nb4CuxSi2B14 alloys (x = 0.6, 1.1, 1.6 at.%) in the form of ribbons was investigated. The chemical composition of the materials was established on the basis of the calculated minima of thermodynamic parameters: Gibbs free energy of amorphous phase formation ΔGamorph (minimum at 0.6 at.% of Cu) and Gibbs free energy of mixing ΔGmix (minimum at 1.6 at.% of Cu). The characteristic crystallization temperatures Tx1onset and Tx1 of the alpha-iron phase together with the activation energy Ea for the as-spun samples were determined by differential scanning calorimetry (DSC) with a heating rate of 10–100 °C/min. In order to determine the optimal soft magnetic properties, the wound cores were subjected to a controlled isothermal annealing process in the temperature range of 340–640 °C for 20 min. Coercivity Hc, saturation induction Bs and core power losses at B = 1 T and frequency f = 50 Hz P10/50 were determined for all samples. Moreover, for the samples with the lowest Hc and P10/50, the magnetic losses were determined in a wider frequency range 50 Hz–400 kHz. The real and imaginary parts of the magnetic permeability µ′, µ″ along with the cut-off frequency were determined for the samples annealed at 360, 460, and 560 °C. The best soft magnetic properties (i.e., the lowest value of Hc and P10/50) were observed for samples annealed at 460 °C, with Hc = 4.88–5.69 A/m, Bs = 1.18–1.24 T, P10/50 = 0.072–0.084 W/kg, µ′ = 8350–10,630 and cutoff frequency at 8–9.3 × 104 Hz. The structural study of as-spun and annealed ribbons was carried out using X-ray diffraction (XRD) and a transmission electron microscope (TEM).

Multilayers consisting of graphene oxide (GO) and α-Fe2O3 thin layers were deposited on the ceramic substrates by the spray LbL (layer by layer) coating technique. Graphene oxide was prepared from graphite using the modified Hummers method. Obtained GO flakes reached up to 6 nanometers in thickness and 10 micrometers in lateral size. Iron oxide Fe2O3 was obtained by the wet chemical method from FeCl3 and NH4OH solution. Manufactured samples were deposited as 3 LbL (GO and Fe2O3 layers deposited sequentially) and 6 LbL structures with GO as a bottom layer. Electrical measurements show the decrease of multilayer resistance after the introduction of the oxidizing NO2 gas to the ambient air atmosphere. The concentration of NO2 was changed from 1 ppm to 20 ppm. The samples changed their resistance even at temperatures close to room temperature, however, the sensitivity increased with temperature. Fe2O3 is known as an n-type semiconductor, but the rGO/Fe2O3 hybrid structure behaved similarly to rGO, which is p-type. Both chemisorbed O2 and NO2 act as electron traps decreasing the concentration of electrons and increasing the effective multilayer conductivity. An explanation of the observed variations of multilayer structure resistance also the possibility of heterojunctions formation was taken into account.

The complex structural and magnetic studies of the annealed rapidly quenched Cu-free Fe72Ni8Nb4Si2B14 alloy (metallic ribbons form) are reported here. Based on the calorimetric results, the conventional heat treatment process (with heating rate 10 °C/min and subsequent isothermal annealing for 20 min) for wound toroidal cores has been optimized to obtain the least lossy magnetic properties (for the minimum value of coercivity and magnetic core losses at 50 Hz). For optimal conditions, the complex permeability in the 104–108 Hz frequency range together with core power losses obtained from magnetic induction dependence up to the frequency of 400 kHz was successfully measured. The average and local crystal structure was investigated by the use of the X-ray diffraction method and the transmission electron microscopy observations and proved its fully glassy state. Additionally, for the three temperature values, i.e., 310, 340 and 370 °C, the glass relaxation process study in the function of annealing time was carried out to obtain a deeper insight into the soft magnetic properties: magnetic permeability and cut-off frequency. For this type of Cu-free soft magnetic materials, the control of glass relaxation process (time and temperature) is extremely important to obtain proper magnetic properties.

2D TiO2 thin films and 3D flower-like TiO2-based nanostructures, also decorated with SnO2, were prepared by chemical and thermal oxidation of Ti substrates, respectively. The crystal structure, morphology and gas sensing properties of the TiO2-based sensing materials were investigated. 2D TiO2 thin films crystallized mainly in the form of rutile, while the flower-like 3D nanostructures as anatase. The sensor based on the 2D TiO2 showed the best performance for H2 detection, while the flower-like 3D nanostructures exhibited enhanced selectivity to CO(CH3)2 after sensitization by SnO2 nanoparticles. The sensor response time was of the order of several seconds. Their fast response, high sensitivity to selected gas species, improved selectivity and stability suggest that the SnO2-decorated flower-like 3D nanostructures are a promising material for application as an acetone sensor.

In this paper, the investigation results on preconcentration of acetone at various initial concentrations are presented. The structures were made of conventional materials, such as stainless steel, quartz tube as well as fabricated in MEMS technology - micropreconcentrators. All structures have the same ‘active’ area to obtain more suitable comparison. The adsorbent materials were selected from commercial available Sigma-Aldrich Carbon Adsorbent Sampler Kit, consisting of 8 various adsorbents. The highest concentration factors were obtained by utilization of micropreconcentrator filled with Carboxen-1018, which is recommended for adsorption of C2-C3 compounds. The preconcentrators were placed into microsystem, and semiconductor gas sensor array was used as a detector unit. The microsystem was previously tested and designed for exhaled breath acetone analysis. The obtained results show that micropreconcentrator can be a useful tool for an increasing sensor sensitivity.

Thin-film n-n nanoheterostructures of SnO2/TiO2, highly sensitive to NO2, were obtained in a two-step process: (i) magnetron sputtering, MS followed by (ii) Langmuir-Blodgett, L–B, technique. Thick (200 nm) SnO2 base layers were deposited by MS and subsequently overcoated with a thin and discontinuous TiO2 film by means of L–B. Rutile nanopowder spread over the ethanol/chloroform/water formed a suspension, which was used as a source in L–B method. The morphology, crystallographic and electronic properties of the prepared sensors were studied by scanning electron microscopy, SEM, X-ray diffraction, XRD in glancing incidence geometry, GID, X-ray photoemission spectroscopy, XPS, and uv-vis-nir spectrophotometry, respectively. It was found that amorphous SnO2 films responded to relatively low concentrations of NO2 of about 200 ppb. A change of more than two orders of magnitude in the electrical resistivity upon exposure to NO2 was further enhanced in SnO2/TiO2 n-n nanoheterostructures. The best sensor responses RNO2/R0 were obtained at the lowest operating temperatures of about 120 °C, which is typical for nanomaterials. Response (recovery) times to 400 ppb NO2 were determined as a function of the operating temperature and indicated a significant decrease from 62 (42) s at 123 °C to 12 (19) s at 385 °C A much smaller sensitivity to H2 was observed, which might be advantageous for selective detection of nitrogen oxides. The influence of humidity on the NO2 response was demonstrated to be significantly below 150 °C and systematically decreased upon increase in the operating temperature up to 400 °C.

Fe50Ni28Co17Al11.5Ta2.5 single crystals oriented along the [001] direction were investigated in order to establish the influence of two-step aging conditions on superelastic properties. The homogenized and quenched single crystalline material was subjected to a combination of high-temperature and low-temperature heat treatment at 973 K for 0.5 h and at 723 K for various aging times, respectively. As a result, fine and coherent γ’ precipitates were formed. Using diffraction of high energy synchrotron radiation, the volume fraction of γ’ precipitates was computed while their size was determined by high resolution TEM analysis. Compared with one-step heat treatment, the two-step aging process enables control of the precipitate size in a more accurate way. Moreover, it allows one to obtain a higher volume fraction of precipitates without increasing their size significantly. The obtained coherent γ’ precipitates ranged in size from 5 to 8 nm; that considerably improved mechanical properties. The highest superelastic response was obtained for single crystals aged at 973 K for 0.5 h followed by aging at 723 K for 3 h. The single crystals treated with such conditions exhibited a superelastic strain of 15% in which the mechanical martensite stabilization was substantially suppressed.

In this work, a detailed microstructural investigation of as-melt-spun and heat-treated Fe67Co20B13 ribbons was performed. The as-melt-spun ribbon was predominantly amorphous at room temperature. Subsequent heating demonstrated an amorphous to crystalline α-(Fe,Co) phase transition at 403 °C. In situ transmission electron microscopy observations, carried out at the temperature range of 25–500 °C and with the heating rate of 200 °C/min, showed that the first crystallized nuclei appeared at a temperature close to 370 °C. With a further increase of temperature, the volume of α-(Fe,Co) crystallites considerably increased. Moreover, the results showed that a heating rate of 200 °C/min provides for a fine and homogenous microstructure with the α-(Fe,Co) crystallites size three times smaller than when the ribbon is heated at 20 °C/min. The next step of this research concerned the influence of both the annealing time and temperature on the microstructure and coercivity of the ribbons. It was shown that annealing at 485 °C for a shorter time (2 s) led to materials with homogenous distribution of α-(Fe,Co) crystallites with a mean size of 30 nm dispersed in the residual amorphous matrix. This was reflected in the coercivity (20.5 A/m), which significantly depended on the volume fraction of crystallites, their size, and distribution.

With the rapid advancement of regenerative medicine technologies, there is an urgent need for the development of new, cell-friendly techniques for obtaining nanofibers—the raw material for an artificial extracellular matrix production. We investigated the structure and properties of PCL10 nanofibers, PCL5/PCL10 core-shell type nanofibers, as well as PCL5/PCLAg nanofibres prepared by electrospinning. For the production of the fiber variants, a 5–10% solution of polycaprolactone (PCL) (Mw = 70,000–90,000), dissolved in a mixture of formic acid and acetic acid at a ratio of 70:30 m/m was used. In order to obtain fibers containing PCLAg 1% of silver nanoparticles was added. The electrospin was conducted using the above-described solutions at the electrostatic field. The subsequent bio-analysis shows that synthesis of core-shell nanofibers PCL5/PCL10, and the silver-doped variant nanofiber core shell PCL5/PCLAg, by using organic acids as solvents, is a robust technique. Furthermore, the incorporation of silver nanoparticles into PCL5/PCLAg makes such nanofibers toxic to model microbes without compromising its biocompatibility. Nanofibers obtained such way may then be used in regenerative medicine, for the preparation of extracellular scaffolds: (i) for controlled bone regeneration due to the long decay time of the PCL, (ii) as bioscaffolds for generation of other types of artificial tissues, (iii) and as carriers of nanocapsules for local drug delivery. Furthermore, the used solvents are significantly less toxic than the solvents for polycaprolactone currently commonly used in electrospin, like for example chloroform (CHCl3), methanol (CH3OH), dimethylformamide (C3H7NO) or tetrahydrofuran (C4H8O), hence the presented here electrospin technique may allow for the production of multilayer nanofibres more suitable for the use in medical field.

Equal channel angular pressing (ECAP) method was used for achieving very fine-grained structure and increased mechanical properties of AZ31 magnesium alloy. The experiments were focused on the, in the initial state, hot extruded alloy. ECAP process was realized at the temperature 250°C and following route Bc. It was found that combination of hot extrusion and ECAP leads to producing of material with significantly fine-grained structure and improves mechanical properties. Alloy structure after the fourth pass of ECAP tool with helix matrix 30° shows a fine-grained structure with average grain size of 2 μm to 3 μm and high disorientation between the grains. More experimental results are discussed in this article.

M2 tool steel was used as a feedstock material for casting from the the semisolid range between 1310-1350oC corresponding to 25 - 50 % of the liquid phase. The chemical composition of the investigated steel is following: 0.85%C, 3.9 %Cr, 6.7 %W, 4.7 %Mo and 1.7 % V. A specially constructed machine allowed thixoforming in a protective argon atmosphere and semisolid forming at a high piston velocity powered by a high air pressure. After heating of the feedstock using induction heating by the stamping of semi-liquid sample to a graphite mould pre-heated by resistance heating. The material after thixoforming from 1315oC shows a globular microstructure with a relatively small globule’s size between 30-50 μm. The crystal structure of globules contained, austenite and martensite, while that of the eutectic, ferrite and W2C, Fe3C, Mo2C, M23C6 and VC carbides as determined by X-ray studies and confirmed using electron diffraction studies. The alloying elements like Mo, W and V are concentrated in the eutectic, while Cr only in thixoformed samples segregates to the carbides and indeed M23C6 was identified. The hardness significantly increases up to 780 HV after thixo-forming due to formation of martensite. The other part was cast from the liquid phase at 1450o C using melt spinning method allowing high cooling rate. The microstructure of melt spun ribbon shows a cellular microstructure of austenitic and martensitic structure without the eutectic. The WC and M23C6 carbides were located at the cell’s boundariers. The microhardness near 1300 HV of the ribbon was much higher than that of semisolid formed samples.

Ga⁻Sn⁻Zn eutectic alloy is a non-toxic liquid metal alloy which could be used in a multitude of applications, including as a heat transfer agent, in gas sensing, and in medicine. Alloys containing gallium readily oxidise in air, forming a thin oxide layer that influences the properties of liquid metals and which has not been studied. In this study, the oxide layer formed on Ga⁻Sn⁻Zn alloy was transferred at room temperature onto three substrates—quartz, glass and silicon. The contact angle between the liquid alloy and different substrates was determined. The obtained thin oxide films were characterised using atomic force microscopy, X-ray photon spectroscopy, and optical and transmission electron microscopy. The contact angle does not influence the deposition of the layers. It was determined that it is possible to obtain nanometric oxide layers of a few micrometres in size. The chemical composition was determined by XPS and EDS independently, and showed that the oxide layer contains about 90 atom % of gallium with some additions of tin and zinc. The oxides obtained from the eutectic Ga⁻Sn⁻Zn liquid alloys appear to be nanocrystalline.

V2O5 thin films were deposited onto insulating support (either fused silica or alumina) by means of rf reactive sputtering from a metallic vanadium target. Argon-oxygen gas mixtures of different compositions controlled by the flow rates were used for sputtering. X-ray diffraction at glancing incidence (GIXD) and Scanning Electronic Microscopy (SEM) were used for structural and phase characterization. Optical transmittance and reflectance spectra were recorded with a Lambda 19 Perkin-Elmer double spectrophotometer. Thickness of the films was determined from the profilometry. It has been confirmed by GIXD that the deposited films are composed of V2O5 phase. The estimated optical band gap was ca. 2.5 eV. The gas sensing properties of V2O5 thin films were investigated at RT-690 K towards NO2 gas of 0–20 ppm. The results indicated that material exhibited good response and reversibility towards nitrogen dioxide.

Hot extruded (EX) AZ61 magnesium alloy was processed by the twist channel angular pressing (TCAP) method, which combines equal channel angular pressing (ECAP) and twist extrusion (TE) processes and significantly improves the efficiency of the grain refinement process. Both the initial hot extruded AZ61 alloy and the alloy after completion of TCAP processing were examined by using optical microscopy (OM), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and electron backscatter diffraction (EBSD) and their corresponding micro-tensile testing (M-TT) and hardness testing at room temperature. The results showed that the microstructure of hot extruded alloy was refined well by TCAP due to dynamic recrystallization (DRX) caused by TCAP. The tensile properties, investigated by micro-tensile testing (M-TT), of the AZ61 alloy were significantly improved due to refined microstructure. The highest tensile properties including YS of 240.8 MPa, UTS of 343.6 MPa and elongation of 21.4% of the fine-grained alloy with average grain size below 1.5 µm was obtained after the third TCAP pass at 200 °C using the processing route Bc.