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Yttria oxide

Carl Axel Arrhenius found in 1787 in a quarry near Ytterby, Sweden, a new mineral, which he named ytterbite, and made a summary analysis of it. Further, the Finnish chemist Johan Gadolin isolated in 1794 from this mineral an impure new oxide that he named ytterbia. Friedrich Wohler partly purified the metal yttrium in 1828, whereas Carl Gustaf Mosander separated the oxides of yttrium, erbium and terbium in 1843 from a mixture of yttria oxide. [Pg.1312]

The coatings all contain the stabilized cubic phase. No second phases, tetragonal zirconia or yttria oxide, were detected. With sol-gel processed YSZ, residual porosity was removed after firing at 900°C for 5 h (Okubo, 1996). This densification temperature is lower than in the solid-state preparation where zirconia powders are reacted with yttria powder. [Pg.1510]

In 1843 Mosander showed that yttira could be resolved into the oxides (or earths) of three elements. The name yttria was reserved for the most basic one the others were named erbia and terbia. [Pg.73]

From gadolinite, a mineral named for Gadolin, a Finnish chemist. The rare earth metal is obtained from the mineral gadolinite. Gadolinia, the oxide of gadolinium, was separated by Marignac in 1880 and Lecoq de Boisbaudran independently isolated it from Mosander s yttria in 1886. [Pg.187]

Another sol—gel abrasive, produced by seeding with a-ferric oxide or its precursors, has been patented (30). A magnesium-modified version of this abrasive, also called Cubitron, is being produced as a replacement for the earlier type. Yttria [1314-36-91-vnc>A V eA sol—gel abrasives have also been patented (31), as well as rare earth oxide modified materials (32). These abrasives are all produced by 3M Corporation they have performed very well ia various applications such as ia coated abrasives for grinding stainless steel and exotic alloys. [Pg.12]

A new type of Hquid-phase sintered SiC using yttria [1314-36-9] 2 3 oxide additive and submicrometer SiC powder for enhanced... [Pg.319]

The result is the formation of a dense and uniform metal oxide layer in which the deposition rate is controlled by the diffusion rate of ionic species and the concentration of electronic charge carriers. This procedure is used to fabricate the thin layer of soHd electrolyte (yttria-stabilized 2irconia) and the interconnection (Mg-doped lanthanum chromite). [Pg.581]

TBCs consist of two different materials applied to the hot side of the component a bond coat applied to the surface of the part, and an insulating oxide applied over the bond coat. Characteristics of TBCs are that the insulation is porous, and they have two layers. The first layer is a bond coat of NICrAlY, and the second is a top coat of YTTRIA stabilized Zirconia. [Pg.384]

In 1794 the Finnish chemist J. Gadolin, while examining a mineral that had recently been discovered in a quarry at Ytterby, near Stockholm, isolated what he thought was a new oxide (or earth ) which A. G. Ekeberg in 1797 named yttria. In fact it was a mixture of a number of metal oxides from which yttrium oxide was separated by C. G. Mosander in 1843. This is actually part of the fascinating story of the rare earths to which we shall return in Chapter 30. The first sample of yttrium metal, albeit very impure, was obtained by F. Wohler in 1828 by the reduction of the trichloride by potassium. [Pg.944]

Four years before isolating yttria, Mosander extracted lanthanum oxide as an impurity from cerium nitrate (hence the name from Greek XavOaveiv, to hide), but it was not until 1923 that metallic lanthanum in a relatively pure form was obtained, by electrolysis of fused halides. [Pg.944]

The lanthanides comprise the largest naturally-occurring group in the periodic table. Their properties are so similar that from 1794, when J. Gadolin isolated yttria which he thought was the oxide of a single new element, until 1907, when lutetium was discovered, nearly a hundred claims were made for the discovery of elements... [Pg.1227]

In 1751 the Swedish mineralogist, A. F. Cronstedt, discovered a heavy mineral from which in 1803 M. H. Klaproth in Germany and, independently, i. i. Berzelius and W. Hisinger in Sweden, isolated what was thought to be a new oxide (or earth ) which was named ceria after the recently discovered asteroid, Ceres. Between 1839 and 1843 this earth, and the previously isolated yttria (p. 944), were shown by the Swedish surgeon C. G. Mosander to be mixtures from which, by 1907, the oxides of Sc, Y, La and the thirteen lanthanides other than Pm were to be isolated. The small village of Ytterby near Stockholm is celebrated in the names of no less than four of these elements (Table 30.1). [Pg.1228]

J.K. Hong, I.-H. Oh, S.-A. Hong, and W.Y. Lee, Electrochemical Oxidation of Methanol over a Silver Electrode Deposited on Yttria-Stabilized Zirconia Electrolyte, /. Catal. 163, 95-105 (1996). [Pg.13]

P. Beatrice, C. Pliangos, W.L. Worrell, and C.G. Vayenas, The electrochemical promotion of ethylene and propylene oxidation on Pt deposited on Yttria-Titania-Zirconia, Solid State Ionics 136-137, 833-837 (2000). [Pg.187]

T. Chao, K.J. Walsh, and P.S. Fedkiw, Cyclic voltammetric study of the electrochemical formation of platinum oxide in a Pt/yttria-stabilized zirconia cell, Solid State Ionics 47, 277-285 (1991). [Pg.275]

S. Seimanides, P. Tsiakaras, X.E. Verykios, and C.G. Vayenas, Oxidative Coupling of Methane over Yttria-doped Zirconia Solid Electrolyte, Appl. Catal. 68, 41-53 (1991). [Pg.431]

Other refractory oxides that can be deposited by CVD have excellent thermal stability and oxidation resistance. Some, like alumina and yttria, are also good barriers to oxygen diffusion providing that they are free of pores and cracks. Many however are not, such as zirconia, hafnia, thoria, and ceria. These oxides have a fluorite structure, which is a simple open cubic structure and is particularly susceptible to oxygen diffusion through ionic conductivity. The diffusion rate of oxygen in these materials can be considerable. [Pg.444]

In both cases, we observe an amorphous pattern no crystallites of rare earth oxide appear even at 25% wt. loading. This indicates that oxide particles remain less than 30A in diameter. The surface area, pore volume and pore size distribution of the starting Si-Al support also change on impregnation. Table 1 lists the values for yttria-modified samples of... [Pg.565]

Doped zirconia, yttria and thoria Other oxides (magnesia, alumina, etc.) Electrolytic conductor Nonconductors... [Pg.584]

Another application is in the oxidation of vapour mixtures in a chemical vapour transport reaction, the attempt being to coat materials with a thin layer of solid electrolyte. For example, a gas phase mixture consisting of the iodides of zirconium and yttrium is oxidized to form a thin layer of yttria-stabilized zirconia on the surface of an electrode such as one of the lanthanum-strontium doped transition metal perovskites Lai Sr MO --, which can transmit oxygen as ions and electrons from an isolated volume of oxygen gas. [Pg.242]


See other pages where Yttria oxide is mentioned: [Pg.194]    [Pg.321]    [Pg.323]    [Pg.325]    [Pg.217]    [Pg.122]    [Pg.539]    [Pg.547]    [Pg.429]    [Pg.240]    [Pg.212]    [Pg.213]    [Pg.349]    [Pg.486]    [Pg.366]    [Pg.521]    [Pg.443]    [Pg.92]    [Pg.300]    [Pg.345]    [Pg.439]    [Pg.229]    [Pg.307]    [Pg.17]   
See also in sourсe #XX -- [ Pg.138 ]




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Yttria oxide electrodes

Zirconium oxide yttria-stabilized

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