In the pre-reduction cyclone of the HIsarna process, both thermal decomposition and gas reduction of the injected iron ores occur simultaneously at gas temperatures of 1723–1773 K. In this study, the kinetics of the thermal decomposition of three iron ores (namely OreA, OreB and OreC) for HIsarna ironmaking were analysed as an isolated process with a symmetrical thermogravimetric analyser (TGA) under an inert atmosphere. Using various methods, the chemical and mineralogical composition, particle size distribution, morphology and phase distribution of the ores were analysed. The ores differ in their mineralogy and morphology, where OreA only contains hematite as iron-bearing phase and OreB and OreC include goethite and hematite. To obtain the kinetic parameters in non-isothermal conditions, the Coats–Redfern Integral Method was applied for heating rates of 1, 2 and 5 K/min and a maximum temperature of 1773 K. The TGA results indicate that goethite and hematite decomposition occur as a two-stage process in an inert atmosphere of Ar. The proposed reaction mechanism for the first stage of goethite decomposition is chemical reaction with an activation energy ranging from 46.55 to 60.38 kJ/mol for OreB and from 69.90 to 134.47 kJ/mol for OreC. The proposed reaction mechanism for the second stage of goethite decomposition is diffusion, showing an activation energy ranging between 24.43 and 44.76 kJ/mol for OreB and between 3.32 and 23.29 kJ/mol for OreC. In terms of hematite decomposition, only the first stage was analysed. The proposed reaction mechanism is chemical reaction control. OreA shows an activation energy of 545.47 to 670.50 kJ/mol, OreB one of 587.68 to 831.54 kJ/mol and OreC one of 424.31 to 592.32 kJ/mol.@en

In this study, we experimentally screen a promising class of intermetallic alloys for the electrochemical reduction of CO₂ toward hydrocarbon products. Based on previous DFT-based screening papers, combinations of strongly CO-binding metals such as iron, cobalt, and nickel with weakly CO-binding metals such as gallium, aluminium or zinc were selected as potentially promising catalytic materials. Despite the challenging production of these alloys, we report a general two-step synthesis method for intermetallic alloys and discuss the specific synthesis conditions that must be taken into account when synthesising these materials. After their synthesis, we use a recently developed differential electrochemical mass spectrometry (DEMS) setup to rapidly quantify the CO₂ reduction products over a range of potentials. Almost all newly developed intermetallic catalysts are shown to produce methane and ethylene, while the CoSn catalyst showed higher selectivity towards formate production. However, all tested catalysts mostly produced hydrogen and only reduce CO₂ to a small extent, despite the favourable computational screening results. We discuss possible reasons for this discrepancy and outline a more holistic approach for linking future DFT studies with experiments.

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Boron doped MoSi₂ particles have been envisioned as sacrificial particles for self-healing thermal barrier coatings (TBCs) but their oxidation behaviour is yet not well understood. In this work, oxidation of MoSi₂ based particle is studied in the temperature range of 1050–1200 °C. The oxidation proceeds from a transient to a steady-state oxidation stage. The kinetics during steady-state oxidation is captured with a thermal diffusion-based model. As compared to the oxidation of pure MoSi₂ particles, the addition of boron strongly enhances the silica formation. Also, a finer dispersion of MoB_x in the MoSi₂ matrix accelerates the formation of silica. The oxide growth rate constant increases proportional with the boron content of the MoSi₂ particles. This enhanced oxidation is related to the microstructure of the oxide scale. Upon oxidation, boron yields B₂O₃, which promptly merge with SiO₂ to form amorphous borosilicate, hindering the formation of crystalline SiO₂. Consequently, the migration of oxygen in the borosilicate oxide scale is faster than in the silica oxide scale on pure MoSi₂ particles.

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The pursuit of enhancing NiTi superelasticity through laser powder bed fusion (L-PBF) and [001] texture creation poses a challenge due to increased susceptibility to hot cracking in the resulting microstructure with columnar grains. This limitation restricts NiTi's application and contributes to material waste. To overcome this, we introduce a pioneering approach: utilising spark plasma sintering (SPS) to heal directional cracks in [001] textured L-PBF NiTi shape memory alloy. Diffusion bonding and oxygen utilisation for Ti₂NiO_x formation was found to successfully heal the cracks. SPS enhances mechanical properties, superelasticity at higher temperatures, and two-way shape memory strain during thermomechanical cycling. This work provides an alternative solution for healing cracks in L-PBF parts, enabling the sustainable reuse of cracked materials. By implementing SPS, this approach effectively addresses hot cracking limitations, expanding the application potential of L-PBF NiTi parts while improving their functional and mechanical properties.

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To prevent premature triggering of the healing reaction in Mo-Si containing self-healing thermal barrier coating system, an oxygen impenetrable shell (α-Al₂O₃) around the sacrificial healing particles (MoSi₂) is desired. Here an encapsulation method is presented through selective oxidation of Al in Mo(Al_xSi_1-x)₂ particles. Healing particles of Mo(Al_xSi_1-x)₂ is designed in terms of alumina shell thickness, particle size and fraction Al dissolved. By replacing Si by Al in MoSi₂ up to the maximum solubility (x = 0.65) a strong crack healing ability is maintained (relative volume expansion ≥ 40 %). The formed exclusive α-Al₂O₃, featuring a two-layered structure, results from a counter-diffusion process along the grain boundaries, and its oxidation kinetics fits well with the 3D diffusion-Jander model. After 16 h exposure in gaseous ambient with a pO₂ of 5 × 10^-10 atm. at 1100 °C, a closed and dense shell of α-Al₂O₃ is formed with a thickness of about 1.3 µm. The oxide shell produced under this condition provided healing particles with significantly improved stability upon exposure to high pO₂ of 0.2 atm. at 1100 °C for 50 h. The particles after exposure feature an inner core of MoSi₂ with Al completely consumed and an oxide shell of α-Al₂O₃.

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Mo(Al_xSi_1-x)₂ alloy with x in the range of 0.35–0.65 were prepared by a one-step spark plasma sintering. To study the exclusive formation of an α-Al₂O₃ scale, oxidation experiments were conducted in low and high oxygen partial pressure ambient at 1373 K; viz.: 10⁻¹⁴ and 0.21 atm. The oxidation kinetics follows a parabolic rate law after a transient period. A counter-diffusion process of O and Al along grain boundaries of Al₂O₃ scale is responsible for the equiaxed and columnar grain growth based on a two-layered microstructure. The formation of a dense equiaxed α-Al₂O₃ layer contributes to excellent oxidation resistance.

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Boron containing MoSi₂ is a promising material for applications at high temperature, but the oxidation mechanism is still unclear. In this work, the high temperature (1100 °C) oxidation of B doped MoSi₂ in synthetic air has been investigated. A (boro)silicate layer is formed on the surface of the alloy, which features a mixture of amorphous SiO₂ and cristobalite. After an initial transient period, the oxidation kinetics follows a parabolic growth rate law. The growth rate constant of the oxide layer is enhanced by the boron in the alloy by 90 % per at.% B. The increase in growth rate is associated with boron mitigating the formation of cristobalite thereby promoting the formation of amorphous SiO₂.

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Since the oxidation reactions in the process of steel production occur in harsh conditions (i.e., high temperatures and gas atmospheres), it is practically impossible to observe in situ the compositional changes in the steel and the formed oxide scale. Hence, a coupled thermodynamic-kinetic numerical model is developed that predicts the formation of oxide phases and the composition profile of the steel alloy’s constituents in a short time due to external oxidation. The model is applied to high-temperature oxidation of Fe–Mn alloys under different conditions. Oxidizing experiments executed with a thermogravimetric analyzer (TGA) on Fe–Mn alloys with different Mn contents (below 10 wt %) are used to determine kinetic parameters that serve as an input for the model. The mass gain data as a function of time show both linear and parabolic regimes. The results of the numerical simulations are presented. The effect of different parameters, such as temperature, Mn content of the alloy, oxygen partial pressure, and oxidizing gas flow rate on the alloy composition and oxide phases formed, is determined. It is shown that increasing the temperature and decreasing the oxygen partial pressure both lead to a thicker depleted area.

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BiFeO ₃ is a multiferroic material with a perovskite structure that has a lot of potential for use in sensors and transducers. However, obtaining pure single-phase BiFeO ₃ ceramic with a low electrical conductivity via solid-state reactions remains a problem that limits its application. In this work, the suppression of secondary phases in BiFeO ₃ was studied by varying the compositional parameters and the sintering temperature. The addition of 1% Bi ₂O ₃ to the stoichiometric precursor mixture prevented the formation of secondary phases observed when sintering stoichiometric precursors. The pure phase ceramic had a p-type conductivity and a three-decade lower electrical conductivity as measured by impedance spectroscopy. Annealing of optimally synthesized material at different partial pressures of oxygen in an oxygen–nitrogen gas atmosphere showed that the reason for this type of conductivity lies in the high concentration of defects associated with oxygen. By annealing in various mixtures of nitrogen and oxygen, it is possible to control the concentration of these defects and hence the conductivity, which can go down another two decades. At a pO ₂  (Formula presented.) the conductivity is determined by intrinsic charge carriers in the material itself.

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The surface oxidation and wettability of Mn and Si-alloyed steel after annealing at different conditions are studied with scanning electron microscope (SEM), X-ray photoelectron spectroscopy (XPS), and a so-called de-wetting method. After exposure at 950 °C for 1 hour in an Ar + 5 vol pct H₂ gas atmosphere with dew points (DP) ranging from – 40 °C to 10 °C, oxides were observed along the grain boundaries or dispersed on the surface for the Fe–1.8 Mn steels while a continuous oxides layer was formed on Fe–1.9 Mn–0.94 Si steels (composition in weight fractions). The oxides formed at different DPs were predicted based on thermodynamic calculations. (Fe,Mn)O was formed on Fe–1.8 Mn steel at the whole range of DPs, while the oxide phase on Fe–1.9 Mn–0.94 Si steel depends on the DP. At low-DP SiO₂ were formed and with increasing the DP (Fe,Mn)SiO₃ or (Fe,Mn)SiO₃ + (Fe,Mn)₂SiO₄ were formed and finally (Fe,Mn)₂SiO₄ were formed. An increase of the fraction of Fe in the oxide with increasing DP for both steels was observed with XPS analysis. As a measure for the surface wettability, the contact angle of Pb droplets on the annealed steels surfaces was determined with SEM and image analysis software. Also, the contact angle of Pb on pure Fe and on the Mn and Si alloyed steels free of surface oxides was measured for comparison. The results show that the contact angle of Pb on the steel surfaces after annealing decreases with increasing DP. This improved wettability with increasing dew point is related to the Fe fraction of the oxides formed on the surface.

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Abstract: The precipitation of supersaturated solutes at free surfaces in ternary Fe–3Au–4W and binary Fe–3Au and Fe–4W alloys (composition in weight percentage) for different ageing times was investigated at a temperature of 700 °C. The time evolution of the surface precipitation is compared among the three alloys to investigate the interplay between the Au and W solutes in the ternary system. The Au-rich grain-interior surface precipitates show a similar size and kinetics in the Fe–Au–W and Fe–Au alloys, while the W-rich grain-interior surface precipitates show a smaller size and a higher number density in the Fe–Au–W alloy compared to the Fe–W alloy. The kinetics of the precipitation on the external free surface for the ternary Fe–Au–W alloy is compared to the previously studied precipitation on the internal surfaces of the grain-boundary cavities during creep loading of the same alloy. Graphical abstract: [Figure not available: see fulltext.]

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Pulsed laser beam welding was used successfully to join the oxide dispersion-strengthened (ODS) Eurofer steel. The joining was conducted with a laser power of 2500 W and a pulsed duration of 4 ms. With the filler material being used, a minor material loss and microvoids were observed in the joint. The microstructure of the fusion zone consists of dual phase elongated structures. The heat-affected zone has a width of around 0.06 mm with finer grains. The transmission electron microscopy observation reveals that nanoprecipitates are finely distributed in the fusion zone. The tensile strength, yield strength and elongation of the joint are slightly inferior to the base material. The fractography results reveal a typical ductile fracture. The experimental results indicate a reasonable joint from the perspective of both the microstructure and mechanical behaviour.

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The present work deals with oxide dispersion strengthened (ODS) Eurofer steel fabricated by powder metallurgy involving mechanical alloying and spark plasma sintering. A heat treatment route including normalising and tempering was applied to the as-produced steel, based on differential scanning calorimetry (DSC) measurement. The microstructure was characterised by scanning electron microscopy (SEM), electron backscattered diffraction (EBSD), electrolytic extraction, X-ray diffraction (XRD) and transmission electron microscopy (TEM). Thermodynamic calculations conducted using Thermo-Calc software were used to determine the precipitation conditions. The results show that the Vickers microhardness of the sample after the designed heat treatment is more uniform compared to the as-produced condition. A dual phase and bimodal microstructure is formed in the as-produced and tempered steels. M₂₃C₆ and M₆C carbides were found in the as-produced sample while only M₂₃C₆ carbides were observed in the tempered sample. The carbides dissolve and reprecipitate during the heat treatment, preferably at the grain boundaries. Nanosized Y₂O₃ particles were found to be homogenously distributed in the steel matrix, which is crucial for the mechanical properties. The dislocation density in the material is decreased significantly after the normalising and tempering treatment. A yield strength model was developed that includes the strengthening contributions of solid solutes, grain size, dislocation density and nanoparticles. Good agreement is obtained between the experimentally measured and theoretically calculated strength of the as-produced and tempered steels.

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Bones of humans and animals combine two unique features, namely: they are brittle yet have a very high fracture toughness linked to the tortuosity of the crack path and they have the ability to repeatedly heal local fissures such that full recovery of overall mechanical properties is obtained even if the local bone structure is irreversibly changed by the healing process. Here it is demonstrated that Ti₂AlC MAX phase metallo-ceramics also having a bone-like hierarchical microstructure and also failing along zig-zag fracture surfaces similarly demonstrate repeated full strength and toughness recovery at room temperature, even though the (high temperature) healing reaction involves the local formation of dense and brittle alumina within the crack. Full recovery of the fracture toughness depends on the healed zone thickness and process zone size formed in the alumina reaction product. A 3-dimensional finite element method (FEM) analysis of the data obtained from a newly designed wedge splitting test allowed full extraction of the local fracture properties of the healed cracks.

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Pd–Cu alloys have been investigated as promising candidates for hydrogen separation membranes. Surface segregation influences the long-term performance of these membranes since their catalytic effect is mainly controlled by the surface composition. In the present research, surface segregation of Pd-40 at.% Cu alloy in vacuum and various gas atmospheres (H₂, CO and CO₂) was investigated with both XPS and LEISS probing different depths below the surface. Adsorption of H₂ and CO on the surface has a significant impact and the surface segregation trend can be reversed as compared to segregation in vacuum, however, CO₂ has almost no influence on the segregation behaviour. A thermodynamic model is also presented to explain these phenomena and to understand surface segregation behaviour of binary alloys in various gas atmospheres. The results can be considered as basic guidelines to design novel alloys for hydrogen separation membranes and predict their long-term performance under actual working conditions.

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Ternary alloys have been developed for a wide range of applications and surface segregation of ternary alloys has a decisive impact on their performance. Different from binary alloys, in which surface energy is usually the dominant factor, the interaction between solute elements has a noticeable effect on the surface segregation behavior of ternary alloys. As a practical example, Pd-based ternary alloys have been proposed as promising candidates for hydrogen separation membranes due to their excellent permeability and selectivity. In the present work, surface segregation of Pd-Cu-Ag and Pd-Cu-Mo ternary alloys in both vacuum and hydrogen atmosphere is investigated. X-ray photoelectron spectroscopy and low energy ion scattering spectroscopy analyses reveal that the segregation trend of the outermost atomic layer is not always the same as that of the near-surface region. A thermodynamic model is developed to describe the surface segregation of ternary alloys. The results of the model are in good qualitative agreement with experimental results. Furthermore, calculations for other ternary alloy systems confirm that the model provides a simple but universal method for surface segregation in ternary alloys. The results can also be considered as basic guidelines to design novel ternary alloys for various applications.

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Oxide dispersion strengthened (ODS) steels are considered to be one of the candidate structural materials for advanced nuclear applications due to their high elevated-temperature strength, corrosion resistance, and radiation tolerance. Joining of ODS steels by traditional fusion joining techniques is not applicable, because the melting process results in the coarsening of fine grains and agglomeration of nanosized oxide particles, and consequently a significant loss of strength. Spark plasma sintering (SPS) has recently been employed as a novel joining technique, which could be beneficial for joining ODS steels considering the solid state characteristic. A powder metallurgy prepared ODS Eurofer steel was successfully joined using SPS. The microstructure and mechanical properties of the joints were investigated. An almost defect-free joint was obtained at the selected processing condition. The tensile properties of the joints are comparable to the base material. Fracture analysis shows an intergranular fracture in the as-joined sample, while a ductile fracture with well-defined dimples is found in the tempered sample.

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This paper studies the joining of an oxide dispersion strengthened (ODS) steel without destroying the microstructure and thereby deteriorating the mechanical performance. ODS Eurofer was successfully joined by spark plasma sintering (SPS) at 1373 K with a heating rate of 100 K/min and a pressure of 80 MPa. An almost defect-free joint was obtained with a holding time of 40 min and a powder layer between the steel disks. The fine-grained microstructure and homogeneously distributed nanoparticles in the material show no significant change after the joining process. The tensile properties of the joint material are comparable to the base material. SPS has been proven to be a promising technique to join ODS steels due to the good mechanical properties of the joints.

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Oxide dispersion strengthened (ODS)Eurofer steel was prepared via mechanical alloying (MA)and spark plasma sintering (SPS). Different combinations of MA and SPS parameters were adopted in order to optimise the fabrication process. The experimental results show that the sample milled for 30 h, sintered at 1373 K at a pressure of 60 MPa has the highest density and microhardness among all the results obtained. As-produced ODS Eurofer shows a bimodal microstructure with homogeneously dispersed nanoscale Y ₂ O ₃ , that is beneficial for the mechanical properties. The yield and tensile strengths are higher while the elongation is lower in the top and bottom surfaces compared to the middle area of the sample. This is due to the presence of a larger number of M ₂₃ C ₆ carbides, resulting from carbon diffusion from the mould material. As-produced samples were also subjected to a heat treatment. A good balance is achieved between the strength and ductility of the heat-treated material. Yielding properties comparable to hot isostatic pressing or hot extrusion as reported in the literature, the processing route presented by this study shows potential to produce high performance ODS Eurofer.

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A successful sol-gel process to encapsulate molybdenum di-silicide MoSi₂ particles with a closed and thermally stable Al₂O₃ layer using aluminium tri-sec-butoxide as a precursor is presented. The processing conditions such as precursor selection and temperature were optimized through analysing the interaction of the MoSi₂ particles with the sol. The application of the sol-gel based coating was followed by calcining the coated particles at temperatures between 900 and 1200 °C in Ar. The shell composition and the mechanical stability of the microcapsule were analysed by means of X-ray diffraction, scanning electron microscopy and thermogravimetric analysis. Upon calcining at 1200 °C in Ar, the MoSi₂ core remains intact as it is, covered by an α - alumina shell with a thickness of about 0.6 μm. The stability tests proved that the encapsulate particles are about five times more oxidation resistant than the uncoated MoSi₂ particles.

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