Up-Date of a Thermodynamic Database of the ZrO<Subscript>2</Subscript>-Gd<Subscript>2</Subscript>O<Subscript>3</Subscript>-Y<Subscript>2</Subscript>O<Subscript>3</Subscript>-Al<Subscript>2</Subscript>O<Subscript>3</Subscript> System for TBC Applications

The thermodynamic database of the ZrO₂-Gd₂O₃-Y₂O₃-Al₂O₃ system is up-dated taking into account new data on lattice stabilities of ZrO₂, Gd₂O₃ and Y₂O₃ and heat capacity measurements for the monoclinic phase Gd₄Al₂O₉ and phase with garnet structure Gd₃Al₅O₁₂. New data for the heat capacities of Gd₂Zr₂O₇ (pyrochlore) and GdAlO₃ (perovskite) as well as on the enthalpy of formation of fluorite solid solutions (Zr_1−x Gd _x )O_2−x/2 were found to be in good agreement with calculated results. In comparison with the previous assessment, taking into account new experimental data resulted in a change of the melting character of the Gd₄Al₂O₉ phase from a peritectic one to a congruent one in the Gd₂O₃-Al₂O₃ system. Correspondently, in the ternary system ZrO₂-Gd₂O₃-Al₂O₃, the melting character of the three-phase assemblage Gd₂O₃ (B), Gd₄Al₂O₉ and GdAlO₃ changed from eutectic to transition type U. The T ₀-lines for T/M and F/T diffusionless transformations and driving force of partitioning to equilibrium assemblage T + F were calculated in the ZrO₂-Gd₂O₃-Y₂O₃ system.     

Dependency of fracture toughness of plasma sprayed Al<Subscript>2</Subscript>O<Subscript>3</Subscript> coatings on lamellar structure

The fracture toughness of plasma-sprayed Al₂O₃ coatings in terms of critical strain energy release rate G _Ic was investigated using a tapered double cantilever beam (TDCB) approach. This approach makes the fracture toughness be measured only using the critical fracture load disregarding crack length during test. The Al₂O₃ coatings were deposited under different spray distances and plasma powers to clarify the effect of spray parameters on the G _Ic of the coatings. The fracture surfaces were examined using scanning electron microscope. On the basis of an idealized layer microstructure model for thermal sprayed coatings, the theoretical relationship between the cohesive fracture toughness and microstructure is proposed. The correlation between the calculated fracture toughness and observed value is examined. It was found that the fracture toughness of plasma sprayed Al₂O₃ coatings is not significantly influenced by spray distance up to 110 mm, and further increase in spray distance to 130 mm resulted in large decrease in the fracture toughness of the coatings. The G _Ic value predicted based on the proposed model using lamellar interface mean bonding ratio and the effective surface energy of bulk ceramics agreed well with the observed G _Ic data. Such agreement evidently shows that the fracture toughness of thermally sprayed ceramic coatings at the direction along coating surface is determined by lamellar interface bonding.     

Microstructure Characterization of the FeAl<Subscript>2</Subscript>O<Subscript>4</Subscript>-Based Nanostructured Composite Coating Synthesized by Plasma Spraying Fe<Subscript>2</Subscript>O<Subscript>3</Subscript>/Al Powders

The microstructure of the coating prepared by reactive plasma spraying Fe₂O₃/Al composite powders was characterized by x-ray diffraction, scanning electron microscopy, and transmission electron microscopy. The results indicated that the coating exhibited nanostructured microstructure which consisted of FeAl₂O₄, Fe or Fe solid solution, Al₂O₃ and a little FeAl. In the composite coating, spherical Fe particles (tens of nanometers to hundreds of nanometers) were distributed uniformly within the equiaxed and columnar nanograins FeAl₂O₄ matrix. There were two kinds of Al₂O₃ phases present in the composite coating. One kind was nano-sized Al₂O₃ particles uniformly dispersed within the matrix, forming eutectic structure of (FeAl₂O₄ + γ-Al₂O₃); the other was 1-1.5 μm Al₂O₃ particles embedded individually within the matrix. The composite coating had higher toughness than the conventional microstructured Al₂O₃ coating.     

Mechanical Properties of LaTi<Subscript>2</Subscript>Al<Subscript>9</Subscript>O<Subscript>19</Subscript> and Thermal Cycling Behaviors of Plasma-Sprayed LaTi<Subscript>2</Subscript>Al<Subscript>9</Subscript>O<Subscript>19</Subscript>/YSZ Thermal Barrier Coatings

Recently, extensive efforts have been made to develop new thermal barrier coating (TBC) materials which can operate at temperatures above 1523 K over a long term. In this article, LaTi₂Al₉O₁₉ (LTA) was synthesized by solid-state reaction at 1773 K, and the mechanical properties of the LTA bulk were evaluated. The microhardness is about 14 GPa, comparable to that of YSZ bulk, whereas the Young’s modulus is about 44 GPa, lower than the value of YSZ. However, the fracture toughness of 0.8-1 MPa m^1/2 is much lower than that of bulk YSZ. A double-ceramic-layer LTA/YSZ TBC structure was proposed and the TBC sprayed by plasma spraying. Thermal cycling tests of the TBC specimens were performed at 1373 K with a dwell time of 10 min. The LTA remained good stability with ZrO₂ and Al₂O₃. However, the single layer LTA TBC was cracked at the LTA/bond coat interface after about 300 cycles, due to its poor thermal shock resistance, while the YSZ TBC yielded a lifetime of about 1000 cycles. The LTA/YSZ TBC remained intact even after 3000 cycles, exhibiting a promising potential as new TBC materials.     

Fabrication of Al matrix composite reinforced with submicrometer-sized Al<Subscript>2</Subscript>O<Subscript>3</Subscript> particles formed by combustion reaction between HEMM Al and V<Subscript>2</Subscript>O<Subscript>5</Subscript> composite particles during sintering

To fabricate an Al-V matrix composite reinforced with submicron-sized Al₂O₃ and Al_xV_y (Al₃V, Al₁₀V) phases, high energy mechanical milling (HEMM) and sintering were employed. By increasing the milling time, the size of mechanically milled powder was significantly reduced. In this study, the average powder size of 59 μm for Al, and 178 μm for V₂O₅ decreased with the formation of a new product, Al-Al₂O₃-Al_xV_y, with a size range from 1.3 μm to 2.6 μm formed by the in-situ combustion reaction during sintering of HEM milled Al and V₂O₅ composite powders. The in-situ reaction between Al and V₂O₅ during the HEMM and sintering transformed the Al₂O₃ and Al_xV_y (Al₃V, Al₁₀V) phases. Most of the reduced V reacted with excess the Al to form Al_xV_y (Al₃V, Al₁₀V) with very little V dissolved into Al matrix. By increasing the milling time and weight percentage of V₂O₅, the hardness of the Al-Al₂O₃-Al_xV_y composite sintered at 1173 K increased. The composite fabricated with the HEMM Al-20wt.%V₂O₅ composite powder and sintering at 1173 K for 2 h had the highest hardness.     

Structure and electric property comparison between Ge nanoclusters embedded in Al<Subscript>2</Subscript>O<Subscript>3</Subscript> and Al<Subscript>2</Subscript>O<Subscript>3</Subscript>/ZrO<Subscript>2</Subscript>

Metal-insulator-semiconductor (MIS) structures containing Ge nanocrystals embedded in both Al₂O₃ and ZrO₂/Al₂O₃ are fabricated by an ultra-high vacuum electron-beam evaporation method. Secondary ion mass spectroscopy (SIMS) results indicate that Ge embedded in Al₂O₃ diffuses towards the surface of the Al₂O₃ layer after annealing at 800°C in N₂ ambient for 30 min. Ge embedded in ZrO₂/Al₂O₃ is stable, thus inducing less leakage current. Capacitance voltage studies indicate that annealing can effectively passivate the negatively charged trapping centers. Memory effect of the Ge nanoclusters is verified by hysteresis in the C-V curves in the Al₂O₃/Ge+Al₂O₃/Al₂O₃ and ZrO₂/Ge+Al₂O₃/Al₂O₃ samples. This article is based on a presentation in “The 7th Korea-China Workshop On Advanced Materials” organized by the Korea-China Advanced Materials Cooperation Center and the China-Korea Advanced Materials Cooperation Center, held at Ramada Plaza Jeju Hotel, Jeju Island, Korea on August 24–27, 2003.     

Simulation design for the composition of zirconia composite ceramic tool

The relationship between the fracture toughness increment (ΔK _IC) resulting from toughening mechanisms, such as phase transition, residual stress, geometry effect, and grain bridging, and the volume fraction of zirconia was established to simulate and design the composition of a zirconia-matrix composite tool, thereby avoiding “trial-and-error” experiments. The composition of the ZrO₂/Al₂O₃ ceramic tool was simulated in accordance with the requirement for fracture toughness. It was shown that the simulated result was in agreement with experiment and that the established simulation model was to some extent valid in predicting the composition of the zirconia-matrix composite ceramic tool with dispersed α-Al₂O₃. Thus, a new type of ceramic tool material, a ZrO₂/Al₂O₃ composite, was developed by adding α-Al₂O₃ to ZrO₂ on the basis of the results of the computer simulation.     

Phase Relations in the Al<Subscript>2</Subscript>O<Subscript>3</Subscript>-V<Subscript>2</Subscript>O<Subscript>5</Subscript>-MoO<Subscript>3</Subscript> System in the Solid State. The Crystal Structure of AlVO<Subscript>4</Subscript>

Phase relations in the ternary oxide system Al₂O₃-V₂O₅-MoO₃ in the solid state in air have been investigated by using the x-ray diffraction (XRD) and differential thermal analysis/thermogravimetric (DTA/TG) methods. It was confirmed that in the subsolidus area of the Al₂O₃-V₂O₅-MoO₃ system, there exist seven phases, that is Al₂O₃, V₂O_5(s.s.), MoO₃, AlVO₄, Al₂(MoO₄)₃, AlVMoO₇, and V₉Mo₆O₄₀. Seven fields, in which particular phases coexist at equilibrium, were isolated. The crystal structure of AlVO₄ has been refined from x-ray powder diffraction data. Its space group is triclinic, , Z = 6, with a = 0.65323(1) nm, b = 0.77498(2) nm, c = 0.91233(3) nm, α = 96.175(2)°, β = 107.234(3)°, γ = 101.404(3)°, V = 0.42555 nm³. The crystal structure of the compound is isotypic with FeVO₄. Infrared (IR) spectra of AlVO₄ and FeVO₄ are compared.     

Development and Application of Binary Suspensions in the Ternary System Cr<Subscript>2</Subscript>O<Subscript>3</Subscript>-TiO<Subscript>2</Subscript>-Al<Subscript>2</Subscript>O<Subscript>3</Subscript> for S-HVOF Spraying

Compositions in the system Cr₂O₃-TiO₂-Al₂O₃ are among the most used ceramic materials for thermally sprayed coating solutions. Cr₂O₃ coatings present good sliding wear resistance; Al₂O₃ coatings show excellent insulation behavior and TiO₂ striking corrosion properties. In order to combine these properties, coatings containing more than one oxide are highly interesting. The conventional spraying process is limited to the availability of binary feedstock powders with defined compositions. The use of suspensions offers the opportunity for tailor-made chemical compositions: within the triangle of Cr₂O₃-TiO₂-Al₂O₃, each mixture of oxides can be created. Criteria for the selection of raw materials as well as the relevant aspects for the development of binary suspensions in the Cr₂O₃-TiO₂-Al₂O₃ system to be used as feedstock for thermal spraying are presented. This formulation of binary suspensions required the development of water-based single-oxide suspensions with suitable behavior; otherwise, the interaction between the particles while mixing could lead up to a formation of agglomerates, which affect both the stability of the spray process and the coating properties. For the validation of this formulation procedure, binary Cr₂O₃-TiO₂ and Al₂O₃-TiO₂ suspensions were developed and sprayed using the S-HVOF process. The binary coatings were characterized and discussed in terms of microstructure and microhardness.     

Microstructure of Suspension Plasma Spray and Air Plasma Spray Al2O3-ZrO2 Composite Coatings

Al₂O₃-ZrO₂ coatings were deposited by the suspension plasma spray (SPS) molecularly mixed amorphous powder and the conventional air plasma spray (APS) Al₂O₃-ZrO₂ crystalline powder. The amorphous powder was produced by heat treatment of molecularly mixed chemical solution precursors below their crystallization temperatures. Phase composition and microstructure of the as-synthesized and heat-treated SPS and APS coatings were characterized by XRD and SEM. XRD analysis shows that the as-sprayed SPS coating is composed of α-Al₂O₃ and tetragonal ZrO₂ phases, while the as-sprayed APS coating consists of tetragonal ZrO₂, α-Al₂O₃, and γ-Al₂O₃ phases. Microstructure characterization revealed that the Al₂O₃ and ZrO₂ phase distribution in SPS coatings is much more homogeneous than that of APS coatings.     

Effect of Nano-Si<Subscript>3</Subscript>N<Subscript>4</Subscript> Additives and Plasma Treatment on the Dry Sliding Wear Behavior of Plasma Sprayed Al<Subscript>2</Subscript>O<Subscript>3</Subscript>-8YSZ Ceramic Coatings

In this paper, the effect of nano-Si₃N₄ additives and plasma treatment on the wear behavior of Al₂O₃-8YSZ ceramic coatings was studied. Nano-Al₂O₃, nano-8YSZ (8 wt.% Y₂O₃-stabilized ZrO₂) and nano-Si₃N₄ powders were used as raw materials to fabricate four types of sprayable feedstocks. Plasma treatment was used to improve the properties of the feedstocks. The surface morphologies of the ceramic coatings were observed. The mechanical properties of the ceramic coatings were measured. The dry sliding wear behavior of the Al₂O₃-8YSZ coatings with and without Si₃N₄ additives was studied. Nano-Si₃N₄ additives and plasma treatment can improve the morphologies of the coatings by prohibiting the initiation of micro-cracks and reducing the unmelted particles. The hardness and bonding strength of AZSP (Al₂O₃-18 wt.% 8YSZ-10 wt.% Si₃N₄-plasma treatment) coating increased by 79.2 and 44% compared to those of AZ (Al₂O₃-20 wt.% 8YSZ) coating. The porosity of AZSP coating decreased by 85.4% compared to that of AZ coating. The wear test results showed that the addition of nano-Si₃N₄ and plasma treatment could improve the wear resistance of Al₂O₃-8YSZ coatings.     

Studies on Al<Subscript>2</Subscript>O<Subscript>3</Subscript>/ZrO<Subscript>2</Subscript>/Al<Subscript>2</Subscript>O<Subscript>3</Subscript> high K gate dielectrics applied in a fully depleted SOI MOSFET

Al₂O₃/ZrO₂/Al₂O₃ gate stacks were prepared on ultrathin SOI (Silicon on insulator) substrates by ultrahigh vacuum electron beam evaporation and post-annealed in N₂ at 450°C for 30 min. Three clear nanolaminate layered structure of Al₂O₃(2.1 nm)/ZrO₂(3.5 nm)/Al₂O₃(2.3 nm) was observed with a high-resolution cross-sectional transmission electron microscope (HR-XTEM). High frequency capacitance voltage (C-V) characteristics of a fully depleted (FD) SOI MOS capacitor at 1 and 5 MHz were studied. The minority carriers determine the high frequency C-V properties, which is opposite to the case of bulk MOS capacitors. The series resistance of the SOI substrate is found to be the determinant factor of the high frequency characteristics of FD SOI MOS capacitors. This article is based on a presentation in “The 7th Korea-China Workshop on Advanced Materials” organized by the Korea-China Advanced Materials Cooperation Center and the China-Korea Advanced Materials Cooperation Center, held at Ramada Plaza Jeju Hotel, Jeju Island, Korea on August 24≈27, 2003.     

Phase Relations in the ZrO<Subscript>2</Subscript>-Nd<Subscript>2</Subscript>O<Subscript>3</Subscript>-Y<Subscript>2</Subscript>O<Subscript>3</Subscript> System: Experimental Study and Advanced Thermodynamic Modeling

Phase equilibria in the ZrO₂-Nd₂O₃-Y₂O₃ system at 1523-1873 K have been investigated by x-ray diffraction (XRD) and scanning electron microscopy combined with energy dispersive x-ray spectroscopy (SEM/EDX). Temperatures of phase transformations were determined by differential thermal analysis. Temperatures of invariant reactions in the ZrO₂-Nd₂O₃ system F = A + Pyr and H = F + A were determined as 1763 and 2118 K respectively and thermodynamic parameters of phases were re-assessed. Phase transformations in ternary systems were determined at 1732 K for composition ZrO₂-48.46Nd₂O₃-5.38Y₂O₃ (mol%) and at 1744 and 1881 K for composition ZrO₂-79.09Nd₂O₃-2.75Y₂O₃ (mol%). They were interpreted using XRD investigation before and after DTA as Pyr + B → F, Pyr → F and A → B, respectively. The solubility of the Y₂O₃ in pyrochlore phase was found to exceed 10 mol%. The thermodynamic parameters of the ZrO₂-Nd₂O₃-Y₂O₃ system were reassessed taking into account solubility of Y₂O₃ in the Nd₂Zr₂O₇ pyrochlore phase (Pyr). It is assumed that Y³⁺ substitutes Nd³⁺ and Zr⁴⁺ in their preferentially occupied sublattices. Ternary parameter was introduced into fluorite phase (F) for better reproducing of phase equilibria. Mixing parameters were reassessed for phase A (Nd₂O₃ based solution), monoclinic phase B and cubic phase C (Y₂O₃ based solution). The isothermal sections calculated for the ZrO₂-Nd₂O₃-Y₂O₃ system are in the reasonable agreement with experimental results.     

Obtaining ZrO<Subscript>2</Subscript> + CeO<Subscript><Emphasis Type="Italic">x</Emphasis></Subscript> + TiO<Subscript>2</Subscript>/Ti compositions by plasma-electrolytic oxidation of titanium and investigating their properties

Regularities of the effect produced by Ce₂(SO₄)₃ salt introduced in an aqueous electrolyte containing Zr(SO₄)₂ on the plasma-electrolytic formation of oxide coatings on titanium, their composition, and structure are studied. ZrO₂ + CeO _x + TiO₂ three-phase oxide coatings with a thickness about 10 μm are obtained. The coatings involve ZrO₂ cubic phase. The ZrO₂-to-TiO₂ phase ratio in the coatings can be controlled. The zirconium content in the coatings reaches 20 at %, while that of cerium is 3–5 at %. The surface layer (∼3-nm thick) contains Ce³⁺ (∼30%) and Ce⁴⁺ (∼70%). Pores in the surface part of coatings have diameters around or smaller than 1 μm and are regularly arranged. The obtained systems have a certain catalytic activity with respect to the oxidation of CO to CO₂ at temperatures above 400–450°C. The coatings are corrosion-resistant in chloride-containing environments. The thickness h of coatings depending on the charge Q supplied to the cell is described by the equation h = h ₀(Q/Q ₀) ⁿ , where n = 0.35 and h ₀ is the thickness of the coating formed at Q ₀ = 1 C/cm².     

Tunneling magnetoresistance in sintered Fe<Subscript>3</Subscript>O<Subscript>4</Subscript> samples diluted with Fe and α-Fe<Subscript>2</Subscript>O<Subscript>3</Subscript>

Electric transport and magnetoresistance characteristics were investigated for Fe₃O₄-x Fe(x=0, 10, 20 wt.%) samples and Fe₃O₄-α-Fe₂O₃ samples sintered at 500°C. For composition dependence of Fe₃O₄-x Fe samples, the largest room temperature MR, 3.3% at 10 kOe, was obtained from a Fe₃O₄-10 Fe sample. For the surface heat treatment dependence of Fe₃O₄ powders, the largest room temperature MR, 4% at 10 kOe, was obtained from a Fe₃O₄-α-Fe₂O₃ sample sintered with Fe₃O₄ powders heated at 200°C in air. It was found that these enhanced MR ratios always appear together with the appropriate excess resistance which is regarded as the tunneling barrier. These enhanced MR ratios of Fe₃O₄-10 Fe and Fe₃O₄-α-Fe₂O₃ samples can be explained by the increased interparticle contact sites and the appropriate thickness of α-Fe₂O₃, respectively.     

Superior performance of high-velocity oxyfuel-sprayed nanostructured TiO<Subscript>2</Subscript> in comparison to air plasma-sprayed conventional Al<Subscript>2</Subscript>O<Subscript>3</Subscript>-13TiO<Subscript>2</Subscript>

Air plasma-sprayed conventional alumina-titania (Al₂O₃-13wt.%TiO₂) coatings have been used for many years in the thermal spray industry for antiwear applications, mainly in the paper, printing, and textile industries. This work proposes an alternative to the traditional air plasma spraying of conventional aluminatitania by high-velocity oxyfuel (HVOF) spraying of nanostructured titania (TiO₂). The microstructure, porosity, hardness (HV 300 g), crack propagation resistance, abrasion behavior (ASTM G65), and wear scar characteristics of these two types of coatings were analyzed and compared. The HVOF-sprayed nanostructured titania coating is nearly pore-free and exhibits higher wear resistance when compared with the air plasma-sprayed conventional alumina-titania coating. The nanozones in the nanostructured coating act as crack arresters, enhancing its toughness. By comparing the wear scar of both coatings (via SEM, stereoscope microscopy, and roughness measurements), it is observed that the wear scar of the HVOF-sprayed nanostructured titania is very smooth, indicating plastic deformation characteristics, whereas the wear scar of the air plasma-sprayed alumina-titania coating is very rough and fractured. This is considered to be an indication of a superior machinability of the nanostructured coating.     

HVOF-Sprayed Coatings Engineered from Mixtures of Nanostructured and Submicron Al<Subscript>2</Subscript>O<Subscript>3</Subscript>-TiO<Subscript>2</Subscript> Powders: An Enhanced Wear Performance

In previous studies, it has been demonstrated that nanostructured Al₂O₃-13 wt.%TiO₂ coatings deposited via air plasma spray (APS) exhibit higher wear resistance when compared to that of conventional coatings. This study aimed to verify if high-velocity oxy-fuel (HVOF)-sprayed Al₂O₃-13 wt.%TiO₂ coatings produced using hybrid (nano + submicron) powders could improve even further the already recognized good wear properties of the APS nanostructured coatings. According to the abrasion test results (ASTM G 64), there was an improvement in wear performance by a factor of 8 for the HVOF-sprayed hybrid coating as compared to the best performing APS conventional coating. When comparing both hybrid and conventional HVOF-sprayed coatings, there was an improvement in wear performance by a factor of 4 when using the hybrid material. The results show a significant antiwear improvement provided by the hybrid material. Scanning electron microscopy (SEM) at low/high magnifications showed the distinctive microstructure of the HVOF-sprayed hybrid coating, which helps to explain its excellent wear performance. This article is an invited paper selected from presentations at the 2007 International Thermal Spray Conference and has been expanded from the original presentation. It is simultaneously published in Global Coating Solutions, Proceedings of the 2007 International Thermal Spray Conference, Beijing, China, May 14-16, 2007, Basil R. Marple, Margaret M. Hyland, Yuk-Chiu Lau, Chang-Jiu Li, Rogerio S. Lima, and Ghislain Montavon, Ed., ASM International, Materials Park, OH, 2007.     

Effect of Surface Roughness and Structure Features on Tribological Properties of Electrodeposited Nanocrystalline Ni and Ni/Al<Subscript>2</Subscript>O<Subscript>3</Subscript> Coatings

Metal matrix composite coatings obtained by electrodeposition are one of the ways of improving the surfaces of materials to enhance their durability and properties required in different applications. This paper presents an analysis of the surface topography, microstructure and properties (residual stresses, microhardness, wear resistance) of Ni/Al₂O₃ nanocomposite coatings electrodeposited on steel substrates from modified Watt’s-type baths containing various concentrations of Al₂O₃ nanoparticles and a saccharin additive. The residual stresses measured in the Ni/Al₂O₃ coatings decreased with an increasing amount of the co-deposited ceramics. It was established that the addition of Al₂O₃ powder significantly improved the coatings’ microhardness. The wear mechanism changed from adhesive-abrasive to abrasive with a rising amount of Al₂O₃ particles and coating microhardness. Nanocomposite coatings also exhibited a lower coefficient of friction than that of a pure Ni-electrodeposited coating. The friction was found to depend on the surface roughness, and the smoother surfaces gave lower friction coefficients.     

Phase Equilibria in the System Al<Subscript>2</Subscript>O<Subscript>3</Subscript>-CaO-CoO and Gibbs Energy of Formation of Ca<Subscript>3</Subscript>CoAl<Subscript>4</Subscript>O<Subscript>10</Subscript>

An isothermal section of the system Al₂O₃-CaO-CoO at 1500 K has been established by equilibrating 22 samples of different compositions at high temperature and phase identification by optical and scanning electron microscopy, X-ray diffraction, and energy dispersive spectroscopy after quenching to room temperature. Only one quaternary oxide, Ca₃CoAl₄O₁₀, was identified inside the ternary triangle. Based on the phase relations, a solid-state electrochemical cell was designed to measure the Gibbs energy of formation of Ca₃CoAl₄O₁₀ in the temperature range from 1150 to 1500 K. Calcia-stabilized zirconia was used as the solid electrolyte and a mixture of Co + CoO as the reference electrode. The cell can be represented as: From the emf of the cell, the standard Gibbs energy change for the Ca₃CoAl₄O₁₀ formation reaction, CoO + 3/5CaAl₂O₄ + 1/5Ca₁₂Al₁₄O₃₃ → Ca₃CoAl₄O₁₀, is obtained as a function of temperature: /J mol⁻¹ (±50) = −2673 + 0.289 (T/K). The standard Gibbs energy of formation of Ca₃CoAl₄O₁₀ from its component binary oxides, Al₂O₃, CaO, and CoO is derived as a function of temperature. The standard entropy and enthalpy of formation of Ca₃CoAl₄O₁₀ at 298.15 K are evaluated. Chemical potential diagrams for the system Al₂O₃-CaO-CoO at 1500 K are presented based on the results of this study and auxiliary information from the literature.     

Plasma-sprayed nanostructured Al2O3/TiO2 powders and coatings

Air plasma spray has been used to produce metastable oxide-ceramic powders and coatings, starting with commercially available Al₂O₃/13TiO₂ powder feed. The feed material undergoes rapid melting and homogenization in the high-temperature zone of the plasma jet. A metastablex-Al₂O₃·TiO₂ phase is formed when the molten droplets are quenched on a chilled substrate. The metastable phase has a defect spinel structure and a nanocrystalline grain size. When heated, it decomposes into an equilibrium two-phase structure, consisting ofα-Al₂O₃ andβ-Al₂O₃·TiO₂. Both types of ceramic materials have potential as hard, wear-resistant coatings.