Yttrium Addition Research Articles

Effect of Yttrium Addition on Microstructure and Mechanical Properties of Sr-Modified Low-Si Cast Aluminum Alloy

Effect of Yttrium Addition on Microstructure and Mechanical Properties of Sr-Modified Low-Si Cast Aluminum Alloy

Effect of rare earth yttrium and the deformation process on the thermal deformation behavior and microstructure of pure titanium for cathode rolls

This study explores the challenges associated with microstructural refinement and homogenization control for large titanium cathode rolls utilized in electrolytic copper foil production. An innovative deformation control strategy was developed by incorporating yttrium microalloying within the β→α dual-phase region to refine the hot-deformed microstructure of pure titanium. Gleeble thermal simulation tests were performed to assess the impact of rare earth Y, deformation temperatures (700–900 °C), and interpass cooling rates (5 °C/s, 25 °C/s, and 50 °C/s) on the hot deformation behavior and microstructural evolution of pure titanium. The results reveal that Y2O3 particles generated by the addition of rare earth Y enhance dynamic recrystallization through the particle-stimulated nucleation (PSN) mechanism, effectively pinning grain boundaries and impeding recrystallized grain growth. Increased interpass cooling rates lead to finer grains and higher stored energy. The mechanism for grain refinement during dual-phase deformation is described as follows: β-phase nonrecrystallization temperature deformation → rapid cooling control → α-phase recrystallization deformation control, energy storage, strain-induced dynamic phase transformation (SIDT, α→β), and dynamic recrystallization (DRX). Under experimental conditions of β-phase region deformation at 980 °C → inter-pass cooling rate of 50 °C/s → α-phase region deformation at 750 °C, the addition of rare earth yttrium achieved the most effective grain refinement, reducing the average grain size to 2.56 μm.

RESISTANCE OF HEAT-RESISTANT YTTRIUM-CONTAINING SEALING COATINGS TO MECHANICAL FRACTURE WHEN FORMING CUTTING PATHS

According to the results of tribotechnical tests of coatings made of KNA-82 alloy ligatures with the addition of yttrium of 0.1%, 0.3%, 0.5%, data were obtained that allowed us to establish the nature of changes in the dynamic coefficient of friction over the test period and numerous values of the energy intensity of material wear. The evaluation of coatings formed by the gas-flame and ion-plasma method was based on the following premise. The maximum resistance to mechanical fracture is determined by the manifestation of a constant minimum value of the dynamic coefficient of friction. This serves as an indicator of reduced friction force before reaching the fatigue limit. Another key factor is the number of separated particles produced per unit of integral work during the friction process. These evaluation parameters are lined up in a row by the number of points from 1 to 4. The maximum score corresponds to the maximum resistance, i.e., a lower value of the energy intensity of material wear and the minimum value of the stable friction coefficient. It has been determined that the same coincidence of these parameters according to the scores is almost at all stages of testing (I-III) was the coating formed by the gas-flame method with a yttrium concentration of 0.3%-0.5%. The exception was the coating formed by the ion-plasma method with a yttrium concentration of 0.1% at the fourth stage of testing.

Effect of Y on Oxidation Behavior of Directionally Solidified Ni-Based Single-Crystal Superalloy

The effect of yttrium (Y) addition on the oxidation behavior of a Ni-based directionally solidified single-crystal superalloy is investigated in this study. Isothermal oxidation tests for samples with different levels of Y addition are conducted at 1100 °C in air. The Y content of the samples is determined by the actual pickup amount obtained from an Inductively Coupled Plasma-Atomic Emission Spectrometry test. It is discovered that the addition of Y increases the oxide resistance by the scale of an adhesive double-layer oxide, which is composed of Al2O3 and spinel Ni(Cr,Al)2O4. With 70 ppm of Y addition, the oxidation mass gain decreases from 12.6 g/m2 for the alloy without Y addition to 5.3 g/m2, and the oxidation rate decreases significantly. In addition, the internal nitride disappears after Y doping because of an increase in oxidation scale adherence and a decrease in oxidation products. In this study, the alloy with 660 ppm Y addition demonstrates the best oxidation resistance.

Yttria-doped geopolymers: Environmentally friendly and effective materials for shielding concrete in gamma radiation facilities

The use of geopolymer in place of ordinary Portland cement for concrete design and constructure is gaining attraction due to environmental and health considerations. Geopolymers must have high gamma radiation shielding competence in order for them to be useful for radiation shielding concrete. In an attempt to improve the gamma absorption capacity of a metakaolin-based geopolymer matrix, 10 % (GEO-10Y), and 20 % (G-20Y) yttria (Y2O3) was mixed with GEO through a solid-state reaction process. In this study, the influence of adding yttria on the physical and gamma shielding parameters of GEO was investigated. The densities of GEO, GEO-10Y and GEO-20Y were obtained as 2.28, 2.52 and 2.37 g/cm3, respectively. Through simulation using FLUKA code, the mass attenuation coefficients (MAC) and other relevant shielding quantities were estimated. The MACs of GEO, GEO-10Y, and GEO-20Y were within the range of 0.0213–6.6429 cm2/g, 0.0282–13.3923 cm2/g, and 0.0291–14.5136 cm2/g, respectively. The addition of yttria improved the gamma photon shielding competence of the metakaolin-based geopolymer by increasing the MAC and reducing photon buildup factors within 15 keV–15 MeV photon energy range. The shielding effectiveness of the yttria-doped GEO compares well with conventional shielding materials. Yttria-doped geopolymer can be used to produce effective and environmentally-friendly gamma shielding concrete.

Comparison of High-Temperature Wear Resistance of Gas-Flame and Ion-Plasma Sealing Coatings with 0.1% Yttrium

Wear-resistant sealing coatings of KNA-82 system with 0.1% yttrium addition for hot parts of gas-turbine engines, applied by gas-flame and ion-plasma methods, are considered. The introduction of yttrium increases the operating temperature from 900°C to 1100°C. The methodology of modeling of processes of contact interaction of engine parts under operating conditions has been developed. Tribotechnical tests modeling the contact of the coating surface with the rotor ridge tops and blade feathers have been carried out, after which linear wear has been measured and the results have been statistically processed. The gas-flame coatings show slower wear reduction at temperatures up to 800°C, while both coatings show similar properties at 1100°C. The improved properties are attributed to the formation of phase-like Ni3Y compound in the grain boundaries.

Hot pressing of SiC additivated with Al2O3 and Y2O3

This work investigated the sintering of silicon carbide (SiC) with alumina (Al2O3) and yttria (Y2O3) additives by hot pressing. Mixtures of SiC with 1% and 5% Al2O3 and Y2O3 were used, pressed at 1800 °C and 1850 °C, resulting in specimens that were characterized in terms of density, microstructure, Vickers hardness and fracture toughness. The addition of 5% oxide additives provided greater densification and better mechanical properties. The temperature of 1800 °C proved to be the most effective for sintering due to the microstructure presented. The analysis revealed a homogeneous distribution of additives and grains, concluding that the 5% additive is considerably superior for increasing the densification and mechanical strength of SiC.

Interfacial reaction mechanism between Y-containing DD5 alloy and Al2O3 ceramic during directional solidification process

This study systematically investigated the influence of varying yttrium(Y) additions on the interfacial reaction mechanism between the DD5 superalloy melt and Al2O3-based ceramic molds during directional solidification. The analysis revealed the formation of a complex multilayer reaction layer at the alloy-ceramic interface. The interfacial products changed from CaO·6Al2O3 to a mixture of various yttrium oxides after Y was added. As the reaction time increased, the sequence of interfacial reaction products observed on the surface of Y-containing alloys progressed as follows: Y2O3, Y4Al2O9, YAlO3, and ultimately Y3Al5O12. Increasing the Y additions promoted the formation of a reaction layer with a higher atomic percentage of Y. The interfacial reaction process between the DD5 superalloy and Al2O3-based ceramic molds involved ceramic decomposition and diffusion, Y element diffusion and displacement reactions, Al2O3 dissolution and further diffusion of the Al element. This process resulted in the formation of different yttrium-aluminum oxides and related to the bidirectional erosion of the Y2O3. These interfacial reactions significantly contributed to the consumption of Y element within the alloy.

Effect of Yttrium Additions on the High-Temperature Oxidation Behavior of GH4169 Ni-Based Superalloy.

The effect of the active element yttrium and its content on the oxidation behavior of GH4169 Ni-based superalloy at extreme temperature was studied by isothermal oxidation experiments. The results show that the oxide scale of GH4169 alloy presents a multi-layer structure, in which the continuous and dense Cr2O3 oxide layer is located in the subouter layer (II layer) and the continuous Nb-rich layer is in the subinner layer (III layer). These layers can inhibit the diffusion of oxygen and alloying elements, preventing the further oxidation of the alloy. The appropriate addition of yttrium can promote the selective oxidation of Cr element, reduce the thickness of the oxide scale and the oxidation rate of the alloy, inhibit the formation of voids at the interface of the oxide scale/alloy matrix, improve the resistance of the alloy to spalling as well as the adhesion of the oxide scale, and improve the high-temperature oxidation resistance of the alloy. Of those tested, the alloy containing 0.04 wt.%Y has the lowest oxidation weight gain, the slowest oxidation rate, and less oxide scale spalling. Based on this, the effect of yttrium on the high-temperature oxidation behavior of GH4169 Ni-based superalloy and its mechanism were revealed.

Effects of amorphous phase and yttrium on flash sintering and microstructures of ZrO2–SiO2 ceramic nanocomposites

AbstractFlash sintering has been used to consolidate a wide range of ceramics and ceramic composites. However, flash sintering of ceramic nanocomposite with a substantial amorphous phase is rarely studied. Meanwhile, the effects of yttrium addition on the flash sintering behaviors and microstructures of ZrO2‐based ceramic nanocomposite remain unknown. Herein, ZrO2‐SiO2 crystalline‐amorphous ceramic nanocomposites (CACNs) with different contents of amorphous phase and two types of yttrium dopants were sintered by flash sintering. Results showed that the content of amorphous phase (SiO2) had significant effects on the flash sintering behavior. The CACN with 65 mol% SiO2 was nonflash sinterable due to the high electric resistivity of SiO2, whereas, the CACN with 45 mol% SiO2 can be flash sintered to high densification within 35 seconds. The flash‐sintered CACNs consisted of ZrO2 nanocrystallites distributed in an amorphous SiO2 matrix. Flash sintering enhanced the tetragonal‐to‐monoclinic phase transformation of ZrO2. In addition, influences of yttrium dopant on CACNs were also investigated. Yttrium dopants can rapidly dissolve in ZrO2 lattices and show a tetragonal phase stabilization effect during flash sintering. Firework‐like ZrO2 microcrystallites formed by dendritic growth were observed close to the cathode region, which was attributed to athermal electric field effects and the formation and aggregation of oxygen vacancies at the cathode region. The results would provide guidance for fabricating CACNs via flash sintering.

Effects of Yttrium Addition on Bending Deformation Behavior of Magnesium

Effects of Yttrium Addition on Bending Deformation Behavior of Magnesium

Synergistic influence of cerium and yttrium micro-addition on microstructure and mechanical tensile properties of K465 nickel based superalloy

The microstructures and room temperature tensile properties of a nickel-based cast superalloy K465 were investigated with the cerium (Ce) and cerium + yttrium (Y) additions, respectively. In K465 superalloys, Ce element was found to distribute in the internal grains of K465. And, the Y element was shown to combine towards with the MC carbides. The tensile properties experienced increasement with the addition of Ce and Y, 0.86 % increasement for Ce addition and 8.35 % increasement for Ce + Y addition. The synergistic effect of rare earths element plays a positive role in the mechanical properties of the nickel based superalloy.

Postsynthetic modification of yttria‐stabilized zirconia aerogels with silica coatings for enhanced thermal stability

AbstractMaintaining high surface area and porosity at high temperatures is important when considering aerogels for use in thermal management systems. The mesoporous structure of aerogels results in extremely low thermal conductivity, making them lightweight, high performance insulating materials. Maintaining these properties requires innovative routes to suppress sintering and pore collapse as use temperatures rise. The current work aims to improve the pore structure stability of yttria‐stabilized zirconia aerogels by the addition of a SiO2 coating. The functionalization of surface hydroxyl groups by the addition of SiO2 is hypothesized to mitigate condensation reactions, which are a driving force for shrinkage and pore structure collapse. Zirconia aerogels with 0, 10, and 30 mol% yttria (YO1.5) additions were coated in a tetraethyl orthosilicate (TEOS) solution and exposed to temperatures up to 1200°C. Crystal structure, pore structure, and aerogel morphology were investigated to understand changes in aerogel thermal stability. The SiO2 coating exhibited a greater influence on pore stability over yttria concentration, with specific surface area of the coated aerogels being twice that of the uncoated aerogels up to 1000°C. However, the presence of the SiO2 coating promoted rapid sintering and densification at 1200°C, establishing an upper use temperature for SiO2 and a need to develop other coating chemistries.

Improved hardness of Mg-0.5Ni-xY alloys via grain refinement and formation of LPSO structures

The effect of yttrium addition on the grain refinement, formation of long period stacking ordered (LPSO) structures, and improved hardness in hot extruded Mg99.5-xNi0.5Yx (x = 0, 0.5, and 1 at%) alloys was investigated. It was revealed that with increasing Y content, the volume fraction of the LPSO phase (VLPSO) increased, and the average dynamic recrystallization (DRX) grain size (D) was refined. It was shown and quantified that both VLPSO and D contribute to the improvement of hardness, where the deviation from the Hall-Petch relationship was ascribed to the strengthening effect of VLPSO. The equation of H = 36.7 + 0.64 VLPSO + 35/√D was proposed to quantify the synergistic effects of hardening mechanisms to predict the hardness of Mg99.5-xNi0.5Yx alloys after deformation by hot extrusion.

Microstructural Evolution and Mechanical Properties of Y Added CoCrFeNi High-entropy Alloys Produced by Arc-melting

The CoCrFeNi high entropy alloy (HEA) with face-centered cubic (FCC) crystal structure exhibits excellent ductility values even at cryogenic temperatures. However, since this HEA is relatively weak in strength, it may not meet the requirements of industrial applications in terms of strength-ductility trade-off. Therefore, the systematic addition of yttrium (Y) into CoCrFeNi HEA was investigated in the present study to increase the strength by solid solution and second phase strengthening. The HEAs were produced by vacuum arc melting, suction casting, and subsequent homogenization at 1150 °C for 24 h. The structural development of the HEAs was investigated by using the X-ray diffraction (XRD) technique revealing the formation of a solid solution phase and Ni3Y-type hexagonal structure (HS) second phase. The corresponding microstructure of the HEAs was examined under a scanning electron microscope (SEM) revealing the transformation of the microstructure from elongated grains to nearly equiaxed grains with the increase of Y content from 2 at. % to 4 at. %. The mechanical properties of the HEAs were investigated by using hardness and compression tests. The results exhibited a dramatic increase in the hardness from 143 (±2) HV to 335 (±7) HV and in the yield strength from 130 MPa to 1025 MPa with 4 at. % Y addition. Our study has revealed that the addition of rare earth Y element results in further development in the strength of the CoCrFeNi for potential engineering applications.

Effects of yttrium on microstructures and properties of Cu45.12Zr45.12Al5.76Nb4 bulk metallic glass composites

The effects of yttrium on the microstructures and properties of Cu45.12Zr45.12Al5.76Nb4 bulk metallic glass composites were investigated. It was found that yttrium addition could effectively control the distribution and volume fraction of B2-CuZr precipitated phase in the composites by adjusting the glass-forming ability of the alloys, and suppress the eutectoid decomposition of B2-CuZr.Within 2 at.% yttrium addition, the volume fraction of B2-CuZr precipitation in the glassy matrix decreases significantly with the increase of yttrium content. For more than 2 at.% yttrium addition, the volume fraction of B2-CuZr precipitation increases as yttrium content increases. An optimal amount of yttrium (2–3 at.%) enhances glass-forming ability of the alloy, reduces B2-CuZr precipitation, and obviously improves the agglomeration and distribution uniformity of B2-CuZr in the amorphous matrix. The compressive properties of BMG composites with more than 1 at.% yttrium addition drop considerably, which should be mainly attributed to the abundant and various forms of Y2O3 brittle phase formed in the glassy matrix.

Enhancement of mechanical and physical properties of Cu–Ni composites by various contents of Y2O3 reinforcement

The increasing demand for materials possessing enhanced mechanical strength, high thermal conductivity, and excellent electrical properties has grown significantly. Cu-matrix composites, especially Cu– Ni, present a promising candidate to fulfill these demands. In this study, Cu–Ni composites were successfully synthesized using powder metallurgy with various additions (0–1.5 wt%) of Yttria (Y2O3)-reinforcement aiming to enhance their mechanical, thermal, and electrical properties. The microstructural investigations demonstrated a uniform distribution of Y2O3 particles and a slight increase in porosity of the Cu–Ni matrix. The Cu–Ni composites with 1.5 wt% Y2O3 showed the presence of Cu2NiZn intermetallic compounds, potentially harming their physical and mechanical properties. Y2O3-reinforcement significantly increased the hardness and led to a moderate rise in the yield and ultimate compressive strengths. The results indicated that the Cu–Ni matrix without Y2O3-reinforcement had the highest coefficient of thermal expansion, which decreased with the addition of Y2O3, potentially leading to improved thermal properties of Cu–Ni composites. This study puts an emphasis on the importance of Y2O3 particles dispersion and on the extent of porosity in enhancing the thermal and mechanical properties of Cu–Ni composites.

The effect of yttrium on the microstructure and wear and mechanical properties of Al-20%Sn

The current study aimed to examine the effects of different amounts of yttrium on refining the microstructure and improving the wear and mechanical properties of Al-20%Sn alloy. Microstructural analysis indicated that the addition of yttrium led to the formation of an intermetallic compound, Sn5Y2, within the tin phase, disrupting the continuity of this phase at the grain boundaries. Regarding the mechanical tests, it was found that the addition of yttrium increased the hardness and Young's modulus of the alloy. With 1 wt% yttrium addition, the hardness increased by more than 80 %, and Young's modulus doubled. The addition of yttrium up to 0.5 wt% increased the coefficient of friction and erosive wear weight loss, while higher yttrium contents caused a decrease in these values. The friction coefficient in the alloy with 1 wt% yttrium was even lower than that of the initial alloy.

Yttrium effect on 475 °C brittleness of Fe–13Cr–6Al–2Mo-0.5Nb-0.15Zr alloy

The effect of yttrium on the 475 °C brittleness and microstructure stability of Fe–13Cr–6Al–2Mo-0.5Nb-0.15Zr alloy after long-term aging at 475 °C has been investigated. At the early stage of aging, the nanoscale metastable transition phase precipitates in large quantities. After aging for 10,000 h, the nanophase in the Y-free alloy has completely disappeared, and only a great deal of granular Laves phases are left, while a large number of nanoscale phases still exist in the grain of Y-containing alloys. This is because the addition of yttrium combines with vacancies, hinders the diffusion of Laves phase-forming elements, and has the result that the transformation of nanoscale phases Fe2(Mo0.3Nb0.7)Al to Laves phase is inhibited during the aging process of the Y-containing alloys. During aging, precipitation-free zones (PFZ) are formed in the surrounding area where the Laves phase and grain boundaries exist. The elongation of Y-containing alloys decreases with yttrium content, but it is still higher than that of Y-free alloy. The addition of yttrium improves the aging plasticity and weakens the degree of 475 °C brittleness of the alloy, and the effectiveness is diminished with the yttrium. This plays a key role in the further study of Fe–Cr–Al alloys for fuel cladding materials.

Modification of structural, morphological, and dielectric properties of barium calcium titanate ceramics with yttrium addition

Barium calcium titanate (BCT) ceramics with varying yttrium doping concentrations were fabricated using the solid-state compaction process to explore the attributes of dopants. (Ba0.75Ca0.25) TiO3 and (Ba0.75Ca0.25) (YyTi(1-y)) O3 where, y = 0.00, 0.10, 0.15, and 0.20 ceramics were synthesized by pressing isostatically in pellet press apparatus, then sintered at 1250 °C with consequent cooling in furnace ambient. The structural, morphological, and dielectric properties were characterized using X-ray diffraction (XRD), scanning electron microscopy (SEM), and impedance spectroscopy interpretations, respectively. The XRD analysis revealed that the cubic BCT lattice was transformed into a tetragonal structure with Yttrium doping. Scanning electron microscopy (SEM) disclosed that yttrium doping countered the liquid phase formation of BCT as well as influenced grain development and microstructure, leading to the formation of distinct grain boundaries and improved densification. The average grain size (18–29 nm) of the Y-BCT increases as the doping level rises. At 60 Hz, it was reported that the dielectric constant obtained a maximum value of 70000 with a resistivity of 5 × 108 Ώ-cm for y = 0.15. The manifestation of the secondary phase confirmed from XRD, allocating an easy path for oxygen migration, might be responsible for the rise in oxygen vacancy, higher leakage current, and dielectric loss for y = 0.01. Co-doping of calcium and yttrium in BCT ceramics has modified the basic structure and ameliorated composites' structural stability and dielectric characteristics. The optimized sample, upon demonstrating outstanding efficiency, ought to be employed for specific uses such as energy storage devices and capacitors.