Electrical resistivity, oxidation resistivity and hardness of single crystal compounds in the Er–Rh–B system

Single crystals of ternary borides ErRh₃B (cubic,Pm3m), ErRh₃B₂ (monoclinic, C2/m) and ErRh₄B₄ (tetragonal, P4₂/nmc) have been grown from copper solution by slow cooling method. The electrical resistivity, oxidation resistivity and Vickers microhardness were studied. The electrical resistivities at room temperature of the (100) face of ErRh₃B, (001) face of ErRh₃B₂ and (100) face of ErRh₄B₄ are 25.6 μΩ·cm, 50.0 μΩ·cm and 106.8 μΩ·cm, respectively. According to thermogravimetric and differential thermal analyses, the oxidation of ErRh₃B, ErRh₃B₂ and ErRh₄B₄ start at 1030°C, 373°C and 690°C, respectively. The weight gain of the same compounds after heating in air up to 1200°C is 0.7%, 15.44% and 5.4%, respectively. The values of the Vickers microhardness for the (100) face of ErRh₃B, the (100) face of ErRh₃B₂ and the (110) face of ErRh₄B₄ are 4.8–5.0 GPa, 10.4–10.9 GPa and 10.9–11.3 GPa, respectively. The effect of boron content and crystal structure of each compound on the electrical resistivity, oxidation resistivity and Vickers microhardness are discussed.     

Synthesis temperature of Ba4CuPt2O9 compounds and the influence of their addition on the orientation of the c-axes of fluorine-doped YBCO superconductors

An experimental study has been carried out to investigate the synergistic effect of Ba₄CuPt₂O₉ compounds on the critical current density of fluorine-doped YBCO superconductors. The Ba₄CuPt₂O₉ compounds were synthesized by a solid state reaction. It was found that the synthesis temperature of the Ba₄CuPt₂O₉ compounds was over 800°C, which was higher than that ever reported previously. In addition, the influence of Ba₄CuPt₂O₉ compounds on the critical current density of YBCO superconductors has been investigated using two types of Ba₄CuPt₂O₉ compounds: one is not heat-treated, i.e. source materials; and the other is heat-treated at 950°C. It was found that the former affected the orientation of the c-axes, but the latter did not have an influence on the orientation of the c-axes, but adversely affected the superconductivity of samples quenched at temperatures above 850°C.     

Hot corrosion behavior of detonation gun sprayed Cr3C2–NiCr coatings on Ni and Fe-based superalloys in Na2SO4–60% V2O5 environment at 900 °C

The present work investigates the hot corrosion resistance of detonation gun sprayed (D-gun) Cr₃C₂–NiCr coatings on Superni 75, Superni 718 and Superfer 800 H superalloys. The deposited coatings on these superalloy substrates exhibit nearly uniform, adherent and dense microstructure with porosity less than 0.8%. Thermogravimetry technique is used to study the high temperature hot corrosion behavior of bare and Cr₃C₂–NiCr coated superalloys in molten salt environment (Na₂SO₄–60% V₂O₅) at high temperature 900 °C for 100 cycles. The corrosion products of the detonation gun sprayed Cr₃C₂–NiCr coatings on superalloys are analyzed by using XRD, SEM, and FE-SEM/EDAX to reveal their microstructural and compositional features for elucidating the corrosion mechanisms. It is shown that the Cr₃C₂–NiCr coatings on Ni- and Fe-based superalloy substrates are found to be very effective in decreasing the corrosion rate in the given molten salt environment at 900 °C. Particularly, the coating deposited on Superfer 800 H showed a better hot corrosion protection as compared to Superni 75 and Superni 718. The coatings serve as an effective diffusion barrier to preclude the diffusion of oxygen from the environment into the substrate superalloys. It is concluded that the hot corrosion resistance of the D-gun sprayed Cr₃C₂–NiCr coating is due to the formation of desirable microstructural features such as very low porosity, uniform fine grains, and the flat splat structures in the coating.     

Enhanced superconducting properties of bulk MgB2 prepared by in situ Powder-In-Sealed-Tube method

A systematic study on the superconducting properties of polycrystalline MgB₂ synthesized by in situ Powder-In-Sealed-Tube technique is carried out at different temperatures (750–900 °C). Both XRD and SEM results show well-crystallized MgB₂ grains in all the samples and grain size is found to be increasing with the sintering temperature. Sharp superconducting transitions are observed for all samples, irrespective of sintering temperatures, which implies the high degree phase purity and homogeneity of MgB₂ formed, while J_C(H) plot gives sample dependent critical current density. The samples heat treated at relatively low temperatures show enhanced flux pinning and hence improved J_C(H) performance. The reduced grain size and hence increased density of grain boundary pinning centers of MgB₂ bulks synthesized at low temperature are mainly responsible for the enhanced flux pinning and J_C.     

Comment on “Tritium absorption–desorption characteristics of LaNi4.25Al0.75”

The thermodynamic data for LaNi_4.25Al_0.75 tritide, reported by Wang et al. (W.-d. Wang et al., J. Alloys Compd. (2006), doi:10.1016/j.jallcom.206.09.122), are in variance with our published data. The plateau pressures for the P–C–T isotherms at all temperatures are significantly lower than published data. As a result, the derived thermodynamic parameters, ΔH° and ΔS°, are questionable. Using the thermodynamic parameters derived from the data reported by Wang et al. will result in under estimating the expected pressures, and therefore not to provide the desired performance for storing and processing tritium.     

Investigation of the microwave dielectric properties of Ca1−xMgxLa4Ti5O17 ceramics for application in coplanar patch antenna

In this paper, the dielectric properties of Ca_1−xMg_xLa₄Ti₅O₁₇ ceramics at microwave frequency have been studied. The diffraction peaks of Ca_(1−x)Mg_xLa₄Ti₅O₁₇ ceramics nearly unchanged with x increasing from 0 to 0.03. Similar X-ray diffraction peaks of Ca_0.99Mg_0.01La₄Ti₅O₁₇ ceramic were observed at different sintering temperatures. A maximum density of 5.3 g/cm³ can be obtained for Ca_0.99Mg_0.01La₄Ti₅O₁₇ ceramic sintered at 1500 °C for 4 h. A maximum dielectric constant (_r) and quality factor (Q × f) of Ca_0.99Mg_0.01La₄Ti₅O₁₇ ceramic sintered at 1500 °C for 4 h are 56.3 and 12,300 GHz (at 6.4 GHz), respectively. A near-zero temperature coefficient of resonant frequency (τ_f) of −9.6 ppm/°C can be obtained for Ca_0.99Mg_0.01La₄Ti₅O₁₇ ceramic sintered at 1500 °C for 4 h. The measurement results for the aperture-coupled coplanar patch antenna at 2.5 GHz are presented. With this technique, a 3.33% bandwidth (return loss <−10 dB) with a center frequency at approximately 2.5 GHz has been successfully achieved.     

Thermodynamic Aspects of Iron in Metal Dusting

A theoretical analysis has been conducted into the thermodynamic role of iron and the dependence of possible metal-dusting occurrence on temperature, volumetric ratios of carburizing species CH₄ and CO, and total pressure. The analysis indicates that the equilibrium carbon activity with cementite (a _{C(Fe 3 C/Fe} )) decreases with increasing temperature, and becomes lower than unity in excess of approximately 1000°C. This critical temperature could be the upper-temperature limit for decomposition of cementite in metal dusting. The temperature regime for possible metal dusting in either CH₄–H₂ or CO–CO₂ gas mixtures increases with increasing volumetric ratio of CH₄ or CO. Increasing total pressure leads to a reduction of this temperature regime in CH₄–H₂ but an expansion in CO–CO₂. Comparatively, this temperature regime in CO–CO₂ is shifted more towards lower temperatures, and iron is likely more susceptible to metal-dusting attack in CO–CO₂ due to the higher reverse carbon-activity gradient established.     

Thermo-physical and thermal cycling properties of plasma-sprayed BaLa2Ti3O10 coating as potential thermal barrier materials

Increased turbine inlet temperature in advanced turbines has promoted the development of thermal barrier coating (TBC) materials with high-temperature capability. In this paper, BaLa₂Ti₃O₁₀ (BLT) was produced by solid-state reaction of BaCO₃, TiO₂ and La₂O₃ at 1500 °C for 48 h. BLT showed phase stability between room temperature and 1400 °C. BLT revealed a linearly increasing thermal expansion coefficient with increasing temperature up to 1200 °C and the coefficients of thermal expansion (CTEs) are in the range of 1 × 10^− 5–12.5 × 10^− 6 K^− 1, which are comparable to those of 7YSZ. BLT coatings with stoichiometric composition were produced by atmospheric plasma spraying. The coating contained segmentation cracks and had a porosity of around 13%. The microhardness for the BLT coating is 3.9–4.5 GPa. The thermo-physical properties of the sprayed coating were investigated. The thermal conductivity at 1200 °C is about 0.7 W/mK, exhibiting a very promising potential in improving the thermal insulation property of TBC. Thermal cycling result showed that the BLT TBC had a lifetime of more than 1100 cycles of about 200 h at 1100 °C. The failure of the coating occurred by cracking at the thermally grown oxide (TGO) layer due to severe oxidation of bond coat. Based on the above merits, BLT could be considered as a promising material for TBC applications.     

Self-propagating high-temperature synthesis with post-heat treatment of La1−xSrxFeO3 (x = 0–1) perovskite as catalyst for soot combustion

La_1−xSr_xFeO₃ (x = 0–1) perovskite, Sr-substituted LaFeO₃, was prepared by Self-propagating high-temperature synthesis (SHS) and its catalytic activity for soot combustion was experimentally examined in comparison with that of a conventional Pt/Al₂O₃ catalyst. The products were also characterized by XRD, FE-SEM, and BET specific surface area. The XRD analysis revealed that all the products had a perovskite phase as the major compound, together with intermediate phases with higher x values (x = 0.7–1). The BET specific surface area of the products increased with x. Moreover, the catalytic activity for soot combustion also increased with x, wherein the BET specific surface area appeared an appropriate index for explaining the observed activity. The sample with x = 0.8 exhibited the highest activity for soot combustion among all the SHS products. The soot combustion temperature of this product was as much as 100 °C lower than that of non-catalytic soot combustion. In other words, it had the same activity as that at only 20 °C higher, in comparison to conventional Pt/Al₂O₃ catalyst. More significantly, average apparent activation energy of sample with x = 0.8 calculated by Friedman method using TG/DTA was approximately 15 kJ/mol lower than that of Pt/Al₂O₃ catalyst. This result suggested that La_1−xSr_xFeO₃ has the possibility to be an alternative catalyst to Pt/Al₂O₃ catalyst.     

Effect of quenching on magnetostriction and microstructure of melt-spun Fe83Ga17 alloy

The effect of quenching on magnetostriction and microstructure of melt-spun Fe₈₃Ga₁₇ ribbons was investigated. The results show that magnetostriction of ribbons is greatly improved by heat treatment and the value of λ of ribbons reached nearly −2300 ppm after annealed at 700 °C for 3 h. The XRD analyses reveal that the microstructure of melt-spun Fe₈₃Ga₁₇ alloy ribbons was changed after heat treatment and the transition of A2 + DO₃ → A2 + DO₃ + DO₁₉ occurred at 700 °C for the ribbons. The magnetostriction of Fe₈₃Ga₁₇ ribbons is influenced by the emergence of DO₁₉ structure and the increase of ordered degree, and the variation of crystallinity of A2 phase is also related to the magnetostriction of Fe₈₃Ga₁₇ ribbons.     

Influence of Mg particle size on the reactivity and superconducting properties of in situ MgB2

The effects of starting Mg particle size on the reactivity of Mg with B, and on remnant Mg in in situ MgB₂, and their influence on the superconducting system are studied. Samples were prepared by a powder-in-sealed tube (PIST) method, heat treated at 850 °C for 2 h in air and were characterized using XRD, SEM and magnetization measurements. As the particle size of Mg powder increases, residual Mg increases significantly. The MgB₂ prepared using smaller sized Mg powder does not have any residual Mg and show the best infield critical current density (J_C (H)).     

Thermodynamic study of CVD–ZrO2 phase diagrams

Chemical vapor deposition (CVD) of zirconium oxide (ZrO₂) from zirconium acetylacetonate Zr(acac)₄ has been thermodynamically investigated using the Gibbs’ free energy minimization method and the FACTSAGE program. Thermodynamic data Cp°, ΔH° and S° for Zr(acac)₄ have been estimated using the Meghreblian–Crawford–Parr and Benson methods because they are not available in the literature. The effect of deposition parameters, such as temperature and pressure, on the extension of the region where pure ZrO₂ can be deposited was analyzed. The results are presented as calculated CVD stability diagrams. The phase diagrams showed two zones, one of them corresponds to pure monoclinic phase of ZrO₂ and the other one corresponds to a mix of monoclinic phase of ZrO₂ and graphite carbon.     

Effect of Yb substitution on microstructure, physical and mechanical properties of negative thermal expansion Zr1−xYbxWMoO8−x/2 (x = 0–0.05) ceramic

Cubic Zr_1−xYb_xWMoO_8−x/2 (x = 0–0.05) ceramic was first fabricated by a polymorphous precursor transition method. X-ray diffraction experiment indicates that samples with x ≤ 0.05 are single phase solid solution. The measured bulk density, microstructure, maximal compression strength and Young's modulus are obviously sensitive to Yb substitution level, while none of such sensitivity was found for the lattice parameters, negative thermal expansion coefficients and Vickers hardness. Drilling tests on Zr_0.96Yb_0.04WMoO_7.98 ceramic indicate good machinability, which is often required for quality and shape control in engineering applications.     

N-doped TiO2/ZnO composite powder and its photocatalytic performance for degradation of methyl orange

The N-doped TiO₂/ZnO composite powder with a molar ratio of Ti to Zn of 3/1 was prepared via sol–gel process and then ammonia treated with NH₃ mass fractions of 0%, 7%, and 28% for 24 h at room temperature followed by thermal calcinations in air for 2 h at various temperatures of 500, 600, and 700 °C. The as-prepared composite powder was characterized in detail through thermo-gravimetric analyzer, X-ray diffraction, Fourier transform infrared spectroscopy, scanning electron microscopy, and high-resolution transmission electron microscopy. The results showed that the phase transformation of anatase to rutile has been successfully retarded via the ammonia treating process, leading to the presence of anatase phase in the composite. The particle crystallization of the composite powder was significantly promoted with the increase of the calcining temperature. The photocatalysis evaluation through MO degradation revealed an enhanced photocatalytic activity for the composite powder that might be related to the good crystallization, the presence of anatase phase, and the particle size reduction of the powder.     

Conductivity of a new pyrophosphate Sn0.9Sc0.1(P2O7)1−δ prepared by an aqueous solution method

New pyrophosphate Sn_0.9Sc_0.1(P₂O₇)_1−δ was prepared by an aqueous solution method. The structure and conductivity of Sn_0.9Sc_0.1(P₂O₇)_1−δ have been investigated. XRD analysis indicates that Sn_0.9Sc_0.1(P₂O₇)_1−δ exhibits a 3 × 3 × 3 super structure. It was found that Sn_0.9Sc_0.1(P₂O₇)_1−δ prepared by an aqueous method is not conductive. The total conductivity of Sn_0.9Sc_0.1(P₂O₇)_1−δ in open air is 2.35 × 10⁻⁶ and 2.82 × 10⁻⁹ S/cm at 900 and 400 °C respectively. In wet air, the total conductivity is about two orders of magnitude higher (8.1 × 10⁻⁷ S/cm at 400 °C) than in open air indicating some proton conduction. SnP₂O₇ and Sn_0.92In_0.08(P₂O₇)_1−δ prepared by an acidic method were reported fairly conductive but prepared by similar solution methods are not conductive. Therefore, the conductivity of SnP₂O₇-based materials might be related to the synthetic history. The possible conduction mechanism of SnP₂O₇-based materials has been discussed in detail.     

Mechanical study of metallized polyethylene terephthalate (PET) films

Mechanical properties such as Young's modulus (Y), storage modulus (E′), glass transition temperature (T_g), tensile strength (σ), and yield strength (σ_y) of metallized polyethylene terephthalate (PET) films have been measured using Dynamic Mechanical Analyser (DMA). Commercially available PET film thickness of 20 μm has been used for metallization. Aluminium (Al) and lead (Pb) have been coated separately on PET films by vacuum thermal evaporation method to form metallized PET films. The T_g of Al-PET and Pb-PET films has been found to be 112.3 °C and 111.2 °C respectively whereas T_g of commercial PET film is 89.7 °C. The stress–strain curves of metallized PET films at room temperature and at different elevated temperatures have been taken which show significant temperature dependence. In particular, the yield strength shows a decrement with increasing temperature.     

Synthesis and characterization of Al2O3-Ce0.5Zr0.5O2 powders prepared by chemical coprecipitation method

Al₂O₃-Ce_0.5Zr_0.5O₂ catalytic powders were synthesized by the coprecipitation (ACZ-C) and mechanical mixing (ACZ-M) methods, respectively. As-synthesized powders were characterized by XRD, Raman spectroscopy, surface area and thermogravimetric analyses. It was found that the mixing extent of Al³⁺ ions affected the phase development, texture and oxygen storage capacity (OSC) of the Ce_0.5Zr_0.5O₂ powder. Single phase of ACZ-C could be maintained without phase separation and inhibit α-Al₂O₃ formation up to 1200 °C. The specific surface area value of ACZ-C (81.5 m²/g) was larger than that of ACZ-M (62.1 m²/g) and Ce_0.5Zr_0.5O₂ (17.1 m²/g) powders, which were calcined at 1000 °C. In comparison with ACZ-C and Al₂O₃, which were calcined at high temperature (900–1200 °C), it was found that the degradation rate of specific surface area of ACZ-C was lower than that of Al₂O₃. ACZ-C sample showed a higher thermal stability to resist phase separation and crystallite growth, which enhanced the oxygen storage capacity property for Ce_0.5Zr_0.5O₂ powders.     

Improving leakage currents of Pt/Ba0.8Sr0.2TiO3/Pt capacitors using multilayered structures

Pt/Ba_0.8Sr_0.2TiO₃ (BST)/Pt capacitors fabricated by the sol–gel process generally show abnormally high leakage currents. In this paper, we report the reduction of this leakage current in multilayered sol–gel Pt/BST/Pt thin film capacitors. The multilayered structure also provided the flexibility of adjusting the dielectric constant of the film. The thin films were fabricated by a step-by-step annealing scheme at 750 °C except that the top and bottom layers were annealed at less than 750 °C. The observed results are explained by an amorphous/polycrystalline structure, which was confirmed by scanning electron microscopy and X-ray diffraction analysis.     

Polymer-induced generation and characterization of electrophoretic properties of hollow TiOX nanospheres for electronic paper

Hollow TiO_X nanospheres have been successfully prepared using hollow core–double shell latex particles (poly(styrene-co-methyl methacrylate-co-butyl acrylate-co-methacrylic acid) (abbreviated in poly(St-co-MMA-co-BA-co-MAA)) as template, which involves the deposition of inorganic coating on the surface of hollow core–shell latex particles and subsequent removal of the latex by calcinations in air or ammonia gas. Ti(OBu)₄ was used as precursor for the preparation of hollow TiO_X nanospheres. TEM of white hollow core–double shell polymers particles with an aperture of approximately 225 nm displays the perfect characteristic hollow nanospheres structure of primary core–double shell particles. The formation of TiO_X was confirmed by XRD analysis and hollow structure of the particles was revealed by transmission electron microscopy (TEM). When the calcined temperature was at 800 °C, hollow TiO₂ nanospheres were arranged regularly with the diameter range of 130–170 nm. The electrophoretic properties were characterized by JS94J micro-electrophoresis apparatus. The electrophoretic mobility of white TiO₂ and black TiO hollow spheres in tetrachloroethylene were 1.09 × 10⁻⁵ and 3.12 × 10⁻⁵ cm²/V s, and the zeta potentials were 7.10 and 20.24 mV, respectively. The results show that white TiO₂ particles and black TiO hollow nanoparticles are suitable as electrophoretic particles and possess the application potential in the future electrophoretic display.     

Investigations of GaN metal-oxide-semiconductor capacitors with sputtered HfO2 gate dielectrics

This work elucidates the properties of Al/HfO₂/GaN metal-oxide-semiconductor capacitors using reactively sputtered HfO₂ as a gate dielectric. The influence of GaN surface treatments and the post-annealing of HfO₂ films on the leakage current, flat-band voltage, interface trap densities, dielectric constants, and effective oxide charges of the GaN MOS capacitors are presented. The Ga oxynitride on the surface of GaN was effectively removed by chemical solutions that also slightly reduced the dielectric constant, slightly increased the flat-band voltage, eliminated the hysteresis of the capacitance–voltage measurement, and yielded a similar leakage to that without surface treatment. A highest dielectric constant of HfO₂ (17) was obtained when the sample was annealed at 600 °C for 20 min, while the lowest interface trap density (5.3 × 10¹¹ cm⁻²) was obtained when the sample was annealed at 800 °C for 40 min. The leakage mechanism was well fitted by the Schottky emission and Frenkel–Poole emission models at a lower and higher electric field.