Search Results (44)

The feasibility of producing high-quality zinc phosphate cement based on a frit-sintered mixture of ZnO, SiO₂, MgO, and Bi₂O₃ oxides, with the addition of phosphorous slag and an aqueous solution of orthophosphoric acid as the mixing liquid, was demonstrated. The raw materials used for zinc phosphate cement preparation were investigated using various physicochemical analysis methods. It was found that the phosphorous slag contains silicon oxide (37.6%), aluminum oxide (4.49%), calcium oxide (42.4%), magnesium oxide (2.19%), as well as fluorine (1.94%) and calcium fluoride (4.91%). The slag predominantly consists of an amorphous glassy phase with minor inclusions of crystalline components. During the sintering process, the addition of 1.5–3.0 wt.% phosphorous slag to the frit promotes the formation of low-melting eutectics due to the presence of fluorides, resulting in a 100 °C reduction in the sintering temperature. An optimal zinc phosphate cement powder composition was developed, comprising: ZnO—83.0%, MgO—9.0%, SiO₂—3.5%, Bi₂O₃—3.0%, and phosphorous slag—1.5%. The resulting sintered product exhibited a whiteness of 97.8%, which exceeds that of the reference sample by 2.6%. Upon mixing the powder with the mixing liquid, zinc ions are released first, initiating a chemical reaction that leads to the formation of zinc, magnesium, and aluminum phosphates. The compressive strength of the resulting composite cements ranged from 101.8 to 111.9 MPa, fully complying with the requirements for cement grade as specified in GOST 31578-2012. Full article

This study presents a metallothermic reduction mechanism for fabricating Nd and Nd–Fe alloys at 850–1050 °C using anhydrous NdCl₃ and Ca, which have relatively low melting points. Our method decreased the process temperature while improving the recovery rate of Nd using the thermodynamic parameters of the CaCl₂–KCl–NaCl and Nd–Fe liquid solutions. To reduce the activity of the product (CaCl₂), the optimal composition of the CaCl₂–KCl–NaCl molten salt was $X_{{CaCl}_2}=0.4(X_{KCl}:X_{NaCl}=6:4)$. The molten metal bath (Nd or Nd–Fe) that formed at the bottom of the reaction zone during Nd and Nd–Fe alloy production absorbed metal particles generated in the molten salt during the reaction, thereby facilitating ingot formation. In Nd produced at 1050 °C using 1.2× the stoichiometric amount (by mass) of Ca, the Nd recovery rate was 97.0%. Moreover, in the Nd–Fe alloys produced at 1050 °C targeting eutectic compositions, the Nd recovery rate was 96.3%. Increased Fe contents in the Nd–Fe liquid solution reduced the Nd recovery rates, and the Nd–Fe alloy (Nd recovery rate: 89.8%) was produced at 850 °C, suggesting the possibility of increasing the energy efficiency of the Nd production process. The Nd–Fe alloy produced through this proposed process could be used as a raw material in the NdFeB strip casting process. Full article

The need to reduce energy consumption means that it is necessary to reduce the weight of vehicles. However, a thick wall of massive elements promotes the formation of casting defects, which must be removed by either plastic processing (straightening) or welding methods (surface and internal discontinuities). Basic alloys contain Al and Zn as the main alloying elements. The studies involved an evaluation of the microstructure and properties of alloys at ambient and elevated temperatures. The microstructure observation revealed a dendritic structure with the presence of low-melting eutectic, and intermetallic and Laves phases in the interdendritic areas. The presence of these phases may pose significant limitations during welding work. Thermal conductivity coefficient measurements showed that it is constant at temperatures up to 200 °C and is 49 W/mK for 9% Al and 77 W/mK for 9% Zn. The tensile test reveal that the most favorable tensile strength (120 MPa) occurs at temperatures of 150 °C for the 9% Zn alloy and at 180 °C for the 9% Al alloy. Full article

Diffusion bonding with an interlayer is considered an effective means of obtaining Mg/Al dissimilar alloy joints. However, at low temperatures, it is often impossible to simultaneously achieve joints between the interlayer and Mg/Al under the same bonding parameters. For this reason, the interlayer is usually prefabricated on the substrate, followed by conducting diffusion bonding. Due to the higher diffusion rate of atoms in the liquid phase compared to atoms in the solid phase, creating a liquid phase field in diffusion bonding to reduce diffusion resistance and thus omitting the step of prefabricating the interlayer is a feasible approach. In this study, solid-state diffusion bonding and TLP (transient liquid phase) diffusion bonding were combined. The low-temperature diffusion bonding of the Mg/Al alloy was achieved under the same parameters using a Zn/Sn composite interlayer, utilizing the formation of a Zn-Sn eutectic liquid phase and the complete melting of Sn during heating without requiring a prefabricated interlayer. Unlike conventional composite interlayers used in diffusion bonding, the Sn layer of the Zn/Sn composite interlayer completely melts into liquid and is squeezed out of the bonding interface at the bonding temperature. The Mg/Zn interface was bonded by solid-state diffusion bonding, while the Al/Zn interface was joined through TLP diffusion bonding. Research on the bonding temperature showed that the bonding temperature range was narrow and that variation in the bonding temperature had a significant impact on the microstructure of the joints. Full article

To improve the performance of AlCoCrFeNi_2.1 eutectic high-entropy alloys (EHEA) to meet industrial application requirements, Zr_xAlCoCrFeNi_2.1 high-entropy alloys (x = 0, 0.01, 0.05, 0.1) were synthesized through vacuum induction melting. Their microstructures were analyzed using X-ray diffraction (XRD), scanning electron microscopy (SEM), and energy-dispersive spectroscopy (EDS). Additionally, the hardness, low-temperature compressive properties, nanoindentation creep behavior, and corrosion resistance of these alloys were evaluated. The results showed that AlCoCrFeNi_2.1 is a eutectic high-entropy alloy composed of FCC and B2 phases, with the FCC phase being the primary phase. The addition of Zr significantly affected the phase stability, promoting the formation of intermetallic compounds such as Ni₇Zr₂, which acted as a bridge between the FCC and B2 phases. Zr addition enhanced the performance of the alloy through solid-solution and dispersion strengthening. However, as the Zr content increased, Ni gradually precipitated from the B2 phase, leading to a reduction in the fraction of the B2 phase. Consequently, at x = 0.1, the microhardness and compressive strength decreased at room temperature. Furthermore, a higher Zr content reduced the sensitivity of the alloy to loading rate changes during creep. At x = 0.05, the creep exponent exceeded 3, indicating that dislocation creep mechanisms dominated. In the Zr_xAlCoCrFeNi_2.1 (where x = 0, 0.01, 0.05, 0.1) alloys, when the Zr content is 0.1, the alloy exhibits the lowest self-corrosion current density of 0.034197 μA/cm² and the highest pitting potential of 323.06 mV, indicating that the alloy has the best corrosion resistance. Full article

In additive manufacturing, controlling hot cracking in non-weldable nickel-based superalloys poses a significant challenge for forming complex components. This study introduces a multiple preheating process for the forming surface in electron beam powder bed fusion (EB-PBF), employing a dual-band infrared surface temperature measurement technique instead of the conventional base plate thermocouple method. This new approach reduces the temperature drop during forming, decreasing surface cooling by 28.6% compared to traditional methods. Additionally, the precipitation of carbides and borides is reduced by 38.5% and 80.1%, respectively, lowering the sensitivity to liquefaction cracking. This technique enables crack-free forming at a lower powder bed preheating temperature (1000 °C), thereby improving the powder recycling rate by minimizing powder sintering. Microstructural analysis confirms that this method reduces low-melting eutectic formation and alleviates liquefaction cracking at high-angle grain boundaries caused by thermal cycling. Consequently, crack-free IN738 specimens with high-temperature durability were successfully achieved, providing a promising approach for the EB-PBF fabrication of crack-resistant IN738 components. Full article

Sintering is a common phenomenon, which often takes place during the oxidation roasting process of molybdenite concentrate in multiple-hearth furnaces. The occurrence of sintering phenomena has detrimental effects on the product quality and the service life of the furnace. In this work, the influence of two key factors (roasting temperature and K content) on the sintering behavior is investigated using molybdenite concentrate as the raw material. Different technologies such as XRD, FESEM-EDS, and phase diagrams are adopted to analyze the experimental data. The results show that the higher the roasting temperature is, the greater the mass loss and the more serious the sintering degree will be. The results also show that with the increase in K content, the mass loss of the raw material is first increased and then decreased, while its sintering degree is still gradually increased. The sintering products obtained during the oxidation roasting process are often tightly combined with the bottom of the used crucible with a smooth and dense surface structure, while their internal microstructures are very complicated, which not only includes numerous MoO₃ species, but also unoxidized MoS₂, Mo sub-oxide, SiO₂, and a variety of molybdates. Among them, both MoO₃ and molybdates can be easily dissolved into the ammonia solution, leading to a residue mainly composed of SiO₂ and CaMoO₄. This study also finds that the sintering phenomenon is caused by the increase in local temperature and the formation of various low-melting-point eutectics. It is suggested that decreasing the roasting temperature and K content, especially the K content, are effective methods for reducing the sintering degree of molybdenite concentrate during the oxidation roasting process. Full article

This work is focused on a novel, promising low temperature phase change material (PCM), based on the eutectic Glauber’s salt composition. To allow phase transition within the refrigeration range of temperatures of +5 °C to +12 °C, combined with a high repeatability of melting–freezing processes, and minimized subcooling, the application of three variants of sodium carboxymethyl cellulose (Na-CMC) with distinct molecular weights (700,000, 250,000, and 90,000) is considered. The primary objective is to optimize the stabilization of this eutectic PCM formulation, while maintaining the desired enthalpy level. Preparation methods are refined to ensure repeatability in mixing components, thereby optimizing performance and stability. Additionally, the influence of Na-CMC molecular weight on stabilization is examined through differential scanning calorimetry (DSC), T-history, and rheology tests. The PCM formulation of interest builds upon prior research in which borax, ammonium chloride, and potassium chloride were used as additives to sodium sulfate decahydrate (Glauber’s salt), prioritizing environmentally responsible materials. The results reveal that CMC with molecular weights of 250 kg/mol and 90 kg/mol effectively stabilize the PCM without phase separation issues, slowing crystallization kinetics. Conversely, CMC of 700 kg/mol proved ineffective due to the disruption of gel formation at its low gel point, hindering higher concentrations. Calculations of ionic concentration indicate higher Na ion content in PCM stabilized with 90 kg/mol CMC, suggesting increased ionic interactions and gel strength. A tradeoff is discovered between the faster crystallization in lower molecular weight CMC and the higher concentration required, which increases the amount of inert material that does not participate in the phase transition. After thermal cycling, the best formulation had a latent heat of 130 J/g with no supercooling, demonstrating excellent performance. This work advances PCM’s reliability as a thermal energy storage solution for diverse applications and highlights the complex relationship between Na-CMC molecular weight and PCM stabilization. Full article

Sodium sulfate (Na₂SO₄) is used in the ecofriendly production of sodium sulfide (Na₂S) through H₂ reduction, thereby facilitating the valorization of Na₂SO₄. However, studies on this technique remain at the laboratory stage. This paper proposes a novel process involving the external circulation of Na₂S in a dilute-phase fluidized system to address the low-temperature eutectic formation between Na₂S and Na₂SO₄ during the H₂ reduction of Na₂SO₄ to Na₂S. The process aims to increase the reaction temperature of the Na₂SO₄ while reducing the volume of the liquid phase formed to prevent sintering blockages and enhance the reduction rate. In a proprietary experimental setup, the H₂ reduction process in a dilute-phase fluidized system was investigated. The Na₂S/Na₂SO₄ ratio and reaction temperature were determined to be critical factors influencing the Na₂SO₄ reduction rate. The melting point of the system increased and the amount of liquid phase produced decreased as the Na₂S content was increased to more than 60%. The Na₂S–Na₂SO₄ mixture (mass ratio of 80:20) existed as a solid at the reaction temperature of 740 °C. After roasting for 10 s, the Na₂SO₄ reduction rate reached 93.7% and the Na₂S content in the mixture increased to 98.74%. Full article

To investigate the effect of the sintering temperature on the microstructure characteristics of porous NiTi alloys, two types of porous NiTi alloys with equal atomic ratios were fabricated via elemental powder sintering at 950 °C and 1000 °C. Afterwards, optical microscopy (OM), scanning electron microscopy (SEM) and transmission electron microscopy (TEM) were collectively applied to investigate the pore characteristics and microstructure of the fabricated porous NiTi alloy. The results show that when the sintering temperature increases from 950 °C to 1000 °C, the average pore size increases from 36.00 μm to 181.65 μm, owing to the integration of these newly formed small pores into these pre-existing large-sized pores. The measured density increases from 2.556 g/cm³ to 3.030 g/cm³, while the porosity decreases from 60.4% to 51.8%. This is due to the occurrence of shrinkage after the sufficient diffusion of atoms. Furthermore, the characterization results confirm that a change in the sintering temperature would not change the phase types within a porous NiTi alloy; namely, the matrix consists primarily of B2 NiTi, with a significant amount of Ni₄Ti₃ precipitates and a small amount of Ni₃Ti precipitates and Ti₂Ni precipitates. However, as the sintering temperature increases, the number of Ni₄Ti₃ precipitates decreases significantly. The formation of a Ni₄Ti₃ phase in the present study is closely related to the enrichment of Ni content in the matrix owing to the diffusion rate difference between Ni atoms and Ti atoms and the absence of a transient liquid phase (TLP) during the sintering process owing to the relatively low sintering temperature (lower than the eutectic temperature). Moreover, the increasing sintering temperature speeds up the atom diffusion, which contributes to a reduction in the enrichment of Ni as well as the number of formed Ni₄Ti₃ precipitates. Full article

The pre-sintered preform (PSP) is an advanced technology for repairing the Ni-based superalloy blade in a turbine. In general, boron is added to the Ni-based superalloys in small quantities (<0.1 wt.%) to increase boundary strength and cohesivity. Despite this, the effect of high B content (>1.0 wt.%) on the microstructure evolution and mechanical properties in Ni-based superalloys for the PSP application is rarely studied. The variety, composition and evolution of the precipitates during solution heat treatment in the alloy with high B content were determined by EBSD, EPMA and SEM. The results indicate that Cr, W and Mo-rich M₅B₃ type borides precipitate from the matrix and its area fraction reaches up to about 8%. The area fraction of boride decreases with the prolonging of solution time and the increase of temperature higher than 1120 °C. The borides nearly disappear after solution treatment at 1160 °C for 2 h. The redissolution of boride and eutectic results in the formation of B-rich area with low incipient melting (about 1189 °C). It can bond metallurgically with the blade under the melting point of the blade, which decreases the precipitation of harmful phases of the blade after PSP repairing. The microhardness within the grain in the PSP work-blank first decreases (lower than 1160 °C) and then increases (higher than 1185 °C) with the increase of solution heat treatment temperature due to the dissolving and precipitation of borides. The tensile strength of the combination of PSP work-blank and Mar-M247 matrix at room temperature after solution treatment is related to the area fraction of boride, incipient melting and the cohesion between PSP work-blank and Mar-M247 matrix. Full article

Quality degradation due to the formation and growth of ice crystals caused by temperature fluctuations during storage, transportation, or retailing is a common problem in frozen surimi. While commercial antifreeze is used as an ingredient in frozen surimi, its high sweetness does not meet the contemporary consumer demand for low sugar and low calories. Therefore, the development of new green antifreeze agents to achieve an enhanced frozen-thawed stability of surimi has received more attention. The aim of this study was to develop a cryoprotectant (a mixture of citric acid and trehalose) to enhance the frozen-thawed stability of surimi by inhibiting the oxidative denaturation and structural changes of frozen-thawed mirror carp (Cyprinus carpio L.) surimi myofibrillar protein (MP). The results showed that the amounts of free amine, sulfhydryl, α-helix, intrinsic fluorescence intensity, and thermal stability in the control significantly decreased after five F-T cycles, while the Schiff base fluorescence intensity, amounts of disulfide bonds and surface hydrophobicity significantly increased (p < 0.05). Compared to sucrose + sorbitol (SS), the natural deep eutectic solvents (NADES) effectively inhibited protein oxidation. After five F-T cycles, the α-helix content and Ca²⁺-ATPase activity of the NADES samples were 4.32% and 80.0%, respectively, higher, and the carbonyl content was 17.4% lower than those of the control. These observations indicate that NADES could inhibit oxidative denaturation and enhance the structural stability of MP. Full article

AISI 316L stainless-steel-based tungsten carbide composite layers fabricated via laser metal deposition are used for additive manufacturing. Heat treatment practices such as low-temperature plasma carburizing and nitriding improve the hardness and corrosion resistance of austenitic stainless steels via the formation of expanded austenite, known as the S phase. In the present study, practices to enhance the hardness and corrosion resistances of the stainless-steel parts in the composite layers have been investigated, including single plasma carburizing for 4 h and continuous plasma nitriding for 3.5 h following carburizing for 0.5 h at 400 and 450 °C. The as-deposited composite layers contain solid-solution carbon and eutectic carbides owing to the thermal decomposition of tungsten carbide during the laser metal deposition. The eutectic carbides inhibit carbon diffusion, whereas the original solid-solution carbon contributes to the formation of the S phase, resulting in a thick S phase layer. Both the single carburizing and continuous processes are effective in improving the Vickers surface hardness and corrosion resistance of the composite layers despite containing the solid-solution carbon and eutectic carbides. Full article

Zirconates of rare earth elements have emerged as promising candidates for thermal barrier coatings (TBC). This study investigates the hot corrosion resistance of single-layered ceramic coatings composed of Gd₂Zr₂O₇, Sm₂Zr₂O₇, and Nd₂Zr₂O₇. The coatings were prepared using air plasma spraying and applied to an Inconel [IN] 625 substrate. Experimental assessments were conducted to examine the hot corrosion behaviour by subjecting the coatings to pure magnesium sulfate (MgSO₄) salt at 1000 °C for 24 h and a 50/50 mole percent Na₂SO₄ and MgSO₄ mixture at 900 °C for cyclic durations of 5, 10, 15, and 20 h. This combination of salts creates a highly corrosive environment. This short test was carried out due to the necessity of the initial stages of the destruction process characterization. X-ray diffraction (XRD), scanning electron microscopy (SEM), and energy dispersion spectroscopy (EDS) techniques were utilized to identify and analyse the reaction products. At 1000 °C, no chemical reaction products were observed between MgSO₄ and Gd₂Zr₂O₇, Sm₂Zr₂O₇, and Nd₂Zr₂O₇. However, in the presence of the MgSO₄ + Na₂SO₄ mixture, the zirconate coatings reacted, resulting in the formation of reaction products such as Gd(SO₄)₃, Gd₂O₂SO₄, Gd₂O₃, Sm₂O₂SO₄, Sm₂(SO₄)₃, Sm₂O₃, MgO, Nd₂(SO₄)₃, Na₂O, and m-ZrO₂. These compounds are formed due to the interaction of rare earth oxides with a low-temperature-melting eutectic Na₂SO₄+ (3MgSO₄ × Na₂SO₄) melted at 666 °C. Despite the aggressive nature of the corrosive environment, the decomposition of rare earth zirconates was relatively limited, indicating satisfactory resistance to hot corrosion. Among the zirconate systems studied, Gd₂Zr₂O₇ exhibited the lowest resistance to the MgSO₄ + Na₂SO₄-based corrosive environment, while Sm₂Zr₂O₇ and Nd₂Zr₂O₇ demonstrated better corrosion resistance. Full article

The nucleation and the growth of misoriented micro-structure components in single crystals depend on various process parameters and alloy compositions. Therefore, in this study, the influence of different cooling rates on carbon-free, as well as carbon-containing, nickel-based superalloys was investigated. Castings were carried out using the Bridgman and Bridgman–Stockbarger techniques under industrial and laboratory conditions, respectively, to analyze the impact of temperature gradients and withdrawing rates on six alloy compositions. Here, it was confirmed that eutectics could assume a random crystallographic orientation due to homogeneous nucleation in the residual melt. In carbon-containing alloys, eutectics also nucleated at low surface-to-volume ratio carbides due to the accumulation of eutectic-forming elements around the carbide. This mechanism occurred in alloys with high carbon contents and at low cooling rates. Furthermore, micro-stray grains were formed by the closure of residual melt in Chinese-script-shaped carbides. If the carbide structure was open in the growth direction, they could expand into the interdendritic region. Eutectics additionally nucleated on these micro-stray grains and consequently had a different crystallographic orientation compared with the single crystal. In conclusion, this study revealed the process parameters that induced the formation of misoriented micro-structures, which prevented the formation of these solidification defects by optimizing the cooling rate and the alloy composition. Full article