Microstructure and growth morphology of Frank-Kasper phase in rapidly solidified Mg<Subscript>32</Subscript>Al<Subscript>17</Subscript>Zn<Subscript>32</Subscript> ternary alloys

In the present investigation, the microstructures and growth morphology of Mg₃₂(Al,Zn)₄₉ Frank-Kasper phase in rapidly solidified Mg₃₂Al₁₇Zn₃₂ ternary alloys were studied in detail. The samples were characterised by X-ray diffraction analysis (XRD), scanning electron microscopy (SEM), field-emission scanning electron microscopy (FE-SEM) and energy dispersive spectrum (EDS). The results show that the microstructures mainly consist of Mg₃₂(Al,Zn)₄₉ Frank-Kasper phase and interdendritic Mg-rich Φ-phase. Under rapid solidification condition, Mg₃₂(Al,Zn)₄₉ Frank-Kasper phase reveals a perfect faceted dendritic characteristic in the shape of a three-fold symmetric microstructure with doublet tips in the axes direction. Observations for fracture surfaces show that the growth morphology of Mg₃₂(Al,Zn)₄₉ grains was truncated cubic, and its growth mechanism was also discussed.     

Preparation and optical properties of Y<Subscript>2</Subscript>O<Subscript>3</Subscript>/SiO<Subscript>2</Subscript> powder

Y(NO3)3 and NH3·H2O were used as a raw materials,and nano-Y2O3 powder was successfully synthesized by a precipitation method.Employing TEOS as a raw material,SiO2 powder was successfully prepared by a alkoxide-hydrolysis method,and a Y2O3/SiO2 composite powder was obtained by coating.The Y2O3,SiO2,and Y2O3/SiO2 powders were characterized using X-ray diffraction(XRD),scanning electron microscopy(SEM),and Fourier transform infrared spectrophotometer(FT-IR);the Y2O3 and Y2O3/SiO2 powders were further examined ...     

Corrosion Behavior and Microhardness of Ni-P-SiO<Subscript>2</Subscript>-Al<Subscript>2</Subscript>O<Subscript>3</Subscript> Nano-composite Coatings on Magnesium Alloy

In the present work, nano-composites of Ni-P-SiO₂-Al₂O₃ were coated on AZ91HP magnesium alloy. The surface morphology of the nano-composite coating was studied by field emission scanning electron microscopy (FESEM). The amount of SiO₂ in the coating was determined by energy-dispersive analysis of x-ray (EDX), and the crystalline structure of the coating was examined by x-ray diffractometer (XRD). All the experiments concerning the corrosion behavior of the coating carried out in 3.5 wt.% NaCl solution and evaluated by electrochemical impedance spectroscopy (EIS) and polarization technique. The results showed that an incorporation of SiO₂ and Al₂O₃ in Ni-P coating at the SiO₂ concentration of 10 g/Land 14 g/LAl₂O₃ led to the lowest corrosion rate (i _corr = 1.3 µA/cm²), the most positive E _corr and maximum microhardness (496 VH). Furthermore, Ni-P-SiO₂-Al₂O₃ nano-composite coating possesses less porosity than that in Ni-P coating, resulting in improving corrosion resistance.     

Effect of Y<Subscript>2</Subscript>O<Subscript>3</Subscript> content on the oxidation behavior of Fe-Cr-Al-based ODS alloys

A study was conducted to investigate the cyclic oxidation behavior of two oxide dispersion strengthened (ODS) Fe-Cr-Al based alloys containing 0.17 wt.% and 0.7 wt.% Y₂O₃. The alloys were oxidized in air for 100 h at 1200°C based on a 24 h cycle period. X-ray diffraction (XRD) and analytical transmission electron microscopy (TEM) were used to characterize the structure, morphology, and composition of the oxide scales. Both alloys formed highly adherent and continuous layers of α-Al₂O₃ exhibiting a morphology indicative of inward scale growth. The role of Y₂O₃ was to promote adherence by segregating to the grain boundaries within the oxide. Concurrently, Y₂O₃ generated micro-porosity resulting in a scale of comparatively higher thickness in the alloy with 0.7 wt.% Y₂O₃.     

Experimental Investigation of the Bi-Sb-Zn System: Study of the Isoplethic Sections Bi-SbZn,Bi-Sb<Subscript>3</Subscript>Zn<Subscript>4</Subscript> and Bi-Sb<Subscript>2</Subscript>Zn<Subscript>3</Subscript>

The ceramics based on zinc oxide undergo doping on bismuth and antimony. Exploring the rich part of zinc in the Bi-Sb-Zn system is necessary to know the present phases. For this purpose, an experimental study was carried out by differential scanning calorimetry on alloys belonging to the isopleths Bi-SbZn, Bi-Sb₃Zn₄ and Bi-Sb₂Zn₃.     

Effects of Tungsten Addition on the Microstructure and Mechanical Properties of Near-Eutectic AlCoCrFeNi<Subscript>2</Subscript> High-Entropy Alloy

The effects of tungsten addition on the microstructure and mechanical properties of near-eutectic AlCoCrFeNi₂ high-entropy alloy were investigated in this paper. The AlCoCrFeNi₂W _x alloys comprised the primary BCC phase plus eutectic FCC/BCC phases. It was found that W element can both promote the formation of the primary BCC phase and act as a solid solution strengthening element. The hardness of the AlCoCrFeNi₂W _x alloys increased from HV 293 to HV 356.2 with the increase in W content. The addition of W element improved the strength of alloys but reduced ductility. Thereinto, the AlCoCrFeNi₂W_0.2 alloy showed the most excellent compressive properties with the fracture strength of 2785.9 MPa and the plastic strain of 0.42, respectively, which implied the potential industrial application values.     

Experimental Verification of the Decomposition of Y<Subscript>2</Subscript>O<Subscript>3</Subscript> in Fe-Based ODS Alloys During Mechanical Alloying Process

In this study, we investigated the state of Y₂O₃, as a major additive element in Fe-based ODS alloys, during mechanical alloying (MA) processes by thermodynamic approaches and experimental verification. For this purpose, we introduced Ti₂O₃ that formed different reaction products depending on the state of Y₂O₃ into the Fe-based ODS alloys. In addition, the reaction products of Ti₂O₃, Y, and Y₂O₃ powders were predicted approximately based on their formation enthalpy. The experimental results relating to the formation of Y-based complex oxides revealed that YTiO₃ and Y₂Ti₂O₇ were formed when Ti₂O₃ reacted with Y; in contrast, only Y₂Ti₂O₇ was detected during the reaction between Ti₂O₃ and Y₂O₃. In the alloy of Fe–Cr–Y₂O₃ with Ti₂O₃, YTiO₃ (formed by the reaction of Ti₂O₃ with Y) was detected after the MA and heat treatment processes were complete, even though Y₂O₃ was present in the system. Using these results, it was proved that Y₂O₃ decomposed into monoatomic Y and O during the MA process.     

Porous Y<Subscript>2</Subscript>O<Subscript>3</Subscript> microcubes: synthesis and characterization

In this work, a facile route using a simple solvothermal reaction and sequential heat treatment process to prepare porous Y₂O₃ microcubes is presented. The as-synthesized products were characterized by X-ray powder diffraction (XRD), scanning electronic microscope (SEM), energy dispersive spectrometer (EDS), thermogravimetric analysis (TG), and differential thermal analysis (DTA). The thermal decomposition process of the Y₂O₃ precursor was investigated. SEM results demonstrated that the as-prepared porous Y₂O₃ microcubes were with an average width of about 20 μm and thickness of about 8 μm. It was found that the morphology of the Y₂O₃ precursor could be readily tuned by varying the molar ratio of S₂O₈²⁻ to Y³⁺. Y₂O₃:Eu³⁺ (6.6%) microcubes were also prepared and their photoluminescence properties were investigated.     

Mechanical Properties of Layered La<Subscript>2</Subscript>Zr<Subscript>2</Subscript>O<Subscript>7</Subscript> Thermal Barrier Coatings

Lanthanum zirconate (La₂Zr₂O₇) has been proposed as a promising thermal barrier coating (TBC) material due to its low thermal conductivity and high stability at high temperatures. In this work, both single and double-ceramic-layer (DCL) TBC systems of La₂Zr₂O₇ and 8 wt.% yttria-stabilized zirconia (8YSZ) were prepared using air plasma spray (APS) technique. The thermomechanical properties and microstructure were investigated. Thermal gradient mechanical fatigue (TGMF) tests were applied to investigate the thermal cycling performance. The results showed that DCL La₂Zr₂O₇ + 8YSZ TBC samples lasted fewer cycles compared with single-layered 8YSZ TBC samples in TGMF tests. This is because DCL La₂Zr₂O₇ TBC samples had higher residual stress during the thermal cycling process, and their fracture toughness was lower than that of 8YSZ. Bond strength test results showed that 8YSZ TBC samples had higher bond strength compared with La₂Zr₂O₇. The erosion rate of La₂Zr₂O₇ TBC samples was higher than that of 8YSZ samples, due to the lower critical erodent velocity and fracture toughness of La₂Zr₂O₇. DCL porous 8YSZ + La₂Zr₂O₇ had a lower erosion rate than other SCL and DCL La₂Zr₂O₇ coatings, suggesting that porous 8YSZ serves as a stress-relief buffer layer.     

Processing and Mechanical Properties of Natural Rubber-ZnFe<Subscript>2</Subscript>O<Subscript>4</Subscript> Nanocomposites

We present preliminary results concerning natural rubber reinforced with nanometric ZnFe₂O₄ obtained from an industrial solid waste. The study investigate the influence of these nanometric ceramic particles on the processing as well as the mechanical properties of the obtained rubber composite, opening the possibility of partial replacement of carbon black and exposing a new potential composite material. The hardness of unfilled and reinforced rubber increased as nanometric ZnFe₂O₄ was increased. Besides, tensile properties of the reinforced rubber were measured, observing once again that as the amount of nanometric ZnFe₂O₄ particles was increased, ultimate strength improved from 2.5 MPa to almost 20 MPa.     

Thermal Spray Deposition,Phase Stability and Mechanical Properties of La<Subscript>2</Subscript>Zr<Subscript>2</Subscript>O<Subscript>7</Subscript>/LaAlO<Subscript>3</Subscript> Coatings

This paper deals with the deposition of La₂Zr₂O₇ (LZO) and LaAlO₃ (LAO) mixtures by air plasma spray (APS). The raw material for thermal spray, single phase LZO and LAO in a 70:30 mol.% ratio mixture was prepared from commercial metallic oxides by high-energy ball milling (HEBM) and high-temperature solid-state reaction. The HEBM synthesis route, followed by a spray-drying process, successfully produced spherical agglomerates with adequate size distribution and powder-flow properties for feeding an APS system. The as-sprayed coating consisted mainly of a crystalline LZO matrix and partially crystalline LAO, which resulted from the high cooling rate experienced by the molten particles as they impact the substrate. The coatings were annealed at 1100 °C to promote recrystallization of the LAO phase. The reduced elastic modulus and hardness, measured by nanoindentation, increased from 124.1 to 174.7 GPa and from 11.3 to 14.4 GPa, respectively, after the annealing treatment. These values are higher than those reported for YSZ coatings; however, the fracture toughness (K _IC) of the annealed coating was only 1.04 MPa m^0.5.     

Magnetic properties and crystallization kinetics of Zn<Subscript>0.5</Subscript>Ni<Subscript>0.5</Subscript>Fe<Subscript>2</Subscript>O<Subscript>4</Subscript>

Precursor of nanocrystalline Zn0.5Ni0.5Fe2O4 was obtained by grinding mixture of ZnSO4·7H2O,NiSO4·6H2O,FeSO4·7H2O,and Na2CO3·10H2O under the condition of surfactant polyethylene glycol(PEG)-400 being present at room temperature,washing the mixture with water to remove soluble inorganic salts and drying it at 373 K.The spinel Zn0.5Ni0.5Fe2O4 was obtained via calcining precursor above 773 K.The precursor and its calcined products were characterized by differential scanning calorimetry(DSC) ,Fourier transform infrared(FT-IR) ,X-ray diffraction(XRD) ,and vibrating sample magnetometer(VSM) .The result showed that Zn0.5Ni0.5Fe2O4 obtained at 1073 K had a saturation magnetization of 74 A·m2·kg-1.Kinetics of the crystallization process of Zn0.5Ni0.5Fe2O4 was studied using DSC technique,and kinetic parameters were determined by Kissinger equation and Moynihan et al.equation.The value of the activation energy associated with the crystallization process of Zn0.5Ni0.5Fe2O4 is 220.89 kJ·mol-1.The average value of the Avrami exponent,n,is equal to 1.59±0.13,which suggests that crystallization process of Zn0.5Ni0.5Fe2O4 is the random nucleation and growth of nuclei reaction.     

Effect of Titanium Additions on the Thermophysical Properties of Glass-Forming Cu<Subscript>50</Subscript>Zr<Subscript>50</Subscript> Alloy

Differential scanning calorimetry, laser flash method, and dilatometry were used to study the thermophysical properties of quenched Cu₅₀Zr_50–xTi_x (x = 0, 2, 4, 6, 8) alloys in the temperature range from room temperature to 1100 K. Data obtained on the heat capacity, thermal diffusivity, and density have been used to calculate the coefficient of thermal conductivity. Temperatures corresponding to the stability of martensite CuZr phase, its eutectoid decomposition, and formation in Cu₅₀Zr_50–xTi_x alloys with different Ti contents upon heating have been determined. It has been found that the thermal diffusivity and thermal conductivity of the studied alloys are low and a typical of metallic systems. As the titanium content increases, the coefficients of thermal conductivity and thermal diffusivity vary slightly. It has been shown that the low values of thermophysical characteristics correspond to the better capability of amorphization and can be a criterion for the glass-forming ability of Cu–Zr-based alloys.     

Effect of Heat Treatment on Borides Precipitation and Mechanical Properties of CoCrFeNiAl<Subscript>1.8</Subscript>Cu<Subscript>0.7</Subscript>B<Subscript>0.3</Subscript>Si<Subscript>0.1</Subscript> High-Entropy Alloy Prepared by Arc-Melting and Laser-Cladding

Effects of heat treatment on borides precipitation and mechanical properties of arc-melted and laser-cladded CoCrNiFeAl_1.8Cu_0.7B_0.3Si_0.1 high-entropy alloys were comparatively studied. The arc-melted alloy contains lots of long strip borides distributed in the body-centered cubic phase, with a hardness about 643 HV_0.5. Laser-cladding can effectively inhibit the boride precipitation and the laser-cladded alloy is mainly composed of a simple bcc solid solution, with a high hardness about 769 HV_0.5, indicating the strengthening effect by interstitial boron atoms is greater than the strengthening by borides precipitation. Heat treatments between 800°C and 1200°C can simultaneously improve the hardness and fracture toughness of arc-melted alloys, owing to the boride spheroidization, dissolution, re-precipitation, and hence the increased boron solubility and nano-precipitation in the bcc solid solution. By contrast, the hardness of laser-cladded alloys reduce after heat treatments in the same temperature range, due to the decreased boron solubility in the matrix.     

Phase Formation of the Yttrium Aluminates in the Y<Subscript>2</Subscript>O<Subscript>3</Subscript>-Al<Subscript>2</Subscript>O<Subscript>3</Subscript>-SiC System

Phase formation sequence of the yttrium aluminates in the Y₂O₃-Al₂O₃-SiC ternary system as temperature increases were investigated via x-ray diffraction (XRD). Results showed that YAM (monoclinic), YAP (perovskite) and YAG (garnet) were the yttrium aluminates presented in the solid-state reacted samples at a fixed Al₂O₃:SiC ratio of 1:1. Formation of the yttrium aluminates depended on the temperature. The YAM, YAP and YAG started to form below 1150 °C, at 1300 °C, and at 1450 °C, respectively. Accordingly, two behavior phase diagrams of the Y₂O₃-Al₂O₃-SiC ternary system were recognized, one is in the temperature range of 1150-1300 °C and the other is in 1300-1450 °C, respectively. Thereafter, the phase equilibrium was reached in the temperature range of 1450-1700 °C. Effects of SiC on the phase formation processes in the ternary system were discussed.     

Effect of partial substitution of calcium for yttrium on the structure and properties of the Y<Subscript>0.9</Subscript>Ca<Subscript>0.1</Subscript>Ba<Subscript>2</Subscript>Cu<Subscript>3</Subscript>O<Subscript>6.8</Subscript> superconductor

The crystal structure of the high-temperature Y_1–xCa_xBa₂Cu₃O_6.8 superconductor has been studied in a temperature range of 80–300 K using low-temperature X-ray diffraction analysis; its microstructure has been studied by scanning and transmission electron microscopy. Changes of the bond length in the structure of principal phase and precipitation topology of impurity phases and their compositions have been analyzed. An addition of calcium was shown to increase the environmental tolerance of the principal Y123 phase and its microhardness and ensures the low unchanged coefficient of thermal expansion. All of the facts indicate that the material can be used to manufacture composite superconducting articles.     

Mn-Doped Zn<Subscript>2</Subscript>SiO<Subscript>4</Subscript> Phosphors Synthesis Using Flame Spray Pyrolysis

Zn₂SiO₄:Mn²⁺ particles are used as green phosphors in plasma display panels and cathode ray tubes. In this study, we report the synthesis of zinc silicate phosphors by flame spray pyrolysis using different Zn-sources and under different process conditions. The XRD and luminescence measurement showed the phosphors prepared from Zn-nitrate source to have better crystallinity and emission characteristics. The luminescence properties of the phosphor particles were found to improve both at higher methane flow rates during pyrolysis and at higher annealing temperatures.     

压力对Mg₃Zn₃Y₂相的结构、电子和力学性能影响的第一性原理计算

利用基于密度泛函理论(DFT)的第一性原理计算方法,研究了高压对面心立方化合物Mg3Zn3Y2的结构,弹性和电子性能的影响。在0GPa下优化的晶格常数与其他计算和实验结果相吻合。计算并分析了Mg3Zn3Y2的弹性常数。基于弹性常数的计算结果,推导了Mg3Zn3Y2的体积模量(B),剪切模量(G),杨氏模量(E),泊松比(ν),各向异性指数(A),熔点和硬度。结果表明压力的增加可以促进Mg3Zn3Y2的力学性能。最后,通过的电子态密度的分析,表明随着压力的增加,Mg3Zn3Y2相的结构稳定性降低。     

Processing Parameter Effects and Thermal Properties of Y<Subscript>2</Subscript>Si<Subscript>2</Subscript>O<Subscript>7</Subscript> Nanostructured Environmental Barrier Coatings Synthesized by Solution Precursor Induction Plasma Spraying

The solution precursor plasma spray process, in which a solution of metal salts is axially injected into an induction thermal plasma, is suitable for deposition of nanostructured environmental barrier coatings. The effects of main processing parameters, namely the solution precursor concentration, spraying distance, reactor pressure, and atomization gas flow rate, have been analyzed using D-optimal design of experiments regarding the deposition rate and coating porosity responses. Among these four parameters, the solution precursor concentration had the greatest influent on the coating structure, followed by the spraying distance and reactor pressure, and finally the atomization gas flow rate with a small contribution. It is pointed out that the species that impact on the substrate are agglomerates of nanoparticles. The equivalent thermal conductivity of selected coatings was computed from experimental temperature evolution curves obtained by laser flash thermal diffusivity analysis, using two methods: a multilayer finite-element model with optimization, and a multilayer thermal diffusion model. The results of the two models agree, with coatings exhibiting low thermal conductivity between 0.7 and 1 W/(m K) at 800 °C.     

Investigation of Corrosion Protection Performance of Multiphase PEO (Mg<Subscript>2</Subscript>SiO<Subscript>4</Subscript>, MgO,MgAl<Subscript>2</Subscript>O<Subscript>4</Subscript>) Coatings on Mg Alloy Formed in Aluminate-Silicate- based Mixture Electrolyte

Plasma electrolytic oxidation (PEO) coatings in the aluminate-silicate-based mixture electrolyte solution with different duty cycles were successfully applied on Mg alloy. The corrosion behavior of the samples was evaluated by water contact angle test, potentiodynamic polarization, electrochemical impedance spectroscopy (EIS) and immersion tests. Hydrophobic PEO coating could be obtained by adjusting the duty cycle of the applied electric signal. This coating considerably diminished the Mg dissolution and could enhance the impedance values of Mg alloy in 3.5 wt % NaCl solution. However, the surface of other PEO coated samples showed more hydrophilic properties compared to that of the uncoated sample. Dense structure of the modified PEO multiphase (including Mg₂SiO₄, MgO and MgAl₂O₄ phases) coating and also its appropriate thickness provided an effective barrier to remarkably delay corrosive solution penetration into the PEO coating. This phenomenon led to major decrease in anodic current density of alloy in chloride solution.