Corrosion of niobium-1 percent zirconium alloy and yttria by lithium at high flow velocities

Lithium corrosion of niobium zirconium alloys and yttrium oxides at high flow velocitie

Hot-pressed silicon nitride with various lanthanide oxides as sintering additives

The effects of addition of various lanthanide oxides and their mixture with Y2O3 on the sintering of Si3N4 were investigated. The addition of simple and mixed lanthanide oxides promoted the densification of Si3N4 in hot-pressing at 1800 C under 300-400kg/ centimeters squared for 60 min. The crystallization of yttrium and lanthanide-silicon oxynitrides which was observed inn the sintered body containing yttrium-lanthanide mixed oxides as additives led to the formation of a highly refractory Si3N4 ceramic having a bending strength of 82 and 84 kg/millimeters squared at room temperature and 1300 C respectively. In a Y2O3+La2O3 system, a higher molar ratio of La2O3 to Y2O3 gave a higher hardness and strength at high temperatures. It was found that 90 min was an optimum sintering time for the highest strength

Formation of a microcomposite structure in the surface layer of yttrium-doped titanium

Surface layers containing oxides and carbides of titanium and yttrium are prepared by the electroexplosive doping of titanium with yttrium. The subsequent electron-beam irradiation leads to dispersion of the structure to a nano- and submicron state. The formation of two types of eutectics is revealed using scanning electron microscopy. The eutectics enriched in titanium and yttrium have a globular and plate-like shape, respectively. The formation of a modified surface layer (enriched in yttrium, carbides and oxides of titanium and yttrium) leads to a threefold increase in the microhardness of the titanium, a more than twofold decrease in the friction coefficient of the doped layer, and a more than 2.8-fold decrease in the wear rate

Oxidation resistance of ODS alloy PM2000 from 880°C to 1400°C

Oxidation resistance of ODS alloy PM2000 from 880°C to 1400°

The effect of yttrium and thorium on the oxidation behavior of Ni-Cr-Al alloys

The effect of quaternary additions of 0.5% Y, 0.5 and 1.0% Th to a base alloy of Ni-10CR-5Al on the oxidation behavior and mechanism was studied during oxidation in air over the range of 1000 to 1200 C. The presence of yttrium decreased the oxidation kinetics slightly, whereas, the addition of thorium caused a slight increase. Oxide scale adherence was markedly improved by the addition of the quaternary elements. Although a number of oxides formed on yttrium containing alloys, quantitative X-ray diffraction clearly showed that the rate-controlling step was the diffusion of aluminum through short circuit paths in a thin layer of alumina that formed parabolically with time. Although the scale adherence of the yttrium containing alloy was considerably better than the base alloys, spalling did occur that was attributed to the formation of the voluminous YAG particles which grew in a mushroom-like manner, lifting the protective scale off the subrate locally. The YAG particles formed primarily at grain boundaries in the substrate in which the yttrium originally existed as YNi9

A first-principles study of helium storage in oxides and at oxide--iron interfaces

Density-functional theory calculations based on conventional as well as hybrid exchange-correlation functionals have been carried out to study the properties of helium in various oxides (Al2O3, TiO2, Y2O3, YAP, YAG, YAM, MgO, CaO, BaO, SrO) as well as at oxide-iron interfaces. Helium interstitials in bulk oxides are shown to be energetically more favorable than substitutional helium, yet helium binds to existing vacancies. The solubility of He in oxides is systematically higher than in iron and scales with the free volume at the interstitial site nearly independently of the chemical composition of the oxide. In most oxides He migration is significantly slower and He--He binding is much weaker than in iron. To quantify the solubility of helium at oxide-iron interfaces two prototypical systems are considered (Fe|MgO, Fe|FeO|MgO). In both cases the He solubility is markedly enhanced in the interface compared to either of the bulk phases. The results of the calculations allow to construct a schematic energy landscape for He interstitials in iron. The implications of these results are discussed in the context of helium sequestration in oxide dispersion strengthened steels, including the effects of interfaces and lattice strain.Comment: 13 pages, 10 figures, 4 table

Effect of modification by Pt and manufacturing processes on the microstructure of two NiCoCrAlYTa bond coatings intended for thermal barrier system applications

Few studies have already shown that Pt influences the diffusion of aluminium and therefore the microstructure of β-NiAl or γ-Ni/γ′-Ni3Al materials. Besides, several works have revealed that the addition of Pt to MCrAlY (M = Ni and/or Co) improves the oxidation/corrosion behavior of the material. Nevertheless, very few data have been published on the microstructure of such modified MCrAlYs. Then, the present work deals with the addition of Pt to two NiCoCrAlYTa coatings that differ by their manufacturing process. Characterization is carried out in order to understand the influence of Pt diffusion but also the effect of the manufacturing process on the final microstructure. The collected data from XRD, SEM, EDS and TEM analyses reveal that an Al uphill diffusion occurs during heat treatment due to the presence of the Pt layer. The Al diffusion from the NiCoCrAlYTa bulk to the Pt-rich surface is so extensive that no more β-phase remains within the core of the coating. Pt may also dissolve TaC, precipitates largely present in the non-modified NiCoCrAlYTa coatings. In addition to Pt, the microstructure of the NiCoCrAlYTa prior to Pt deposition and heat treatment, dependent on the NiCoCrAlYTa manufacturing process, greatly influences the final microstructure

Segregation-induced grain boundary electrical potential in ionic oxide materials: A first principles model

A first principles continuum analytical model for cationic segregation to the grain boundaries in complex ceramic oxides is presented. The model permits one to determine the electric charge density and the segregation-induced electric potential profiles through the grain and can be extrapolated to the range of nanostructured grain sizes. The theoretical predictions are compared with existing data for yttria-stabilized tetragonal zirconia polycrystals. The implications for physical properties (mainly high temperature plasticity and hardening behaviour) are then discussed.Gobierno de España MAT2009-14351-C02-01, MAT2009-14351-C02-0