Oxidation cubic

Goldschmidt has classed also with the ionic crystals the C-modification of the sesqui-oxides, cubic crystals with 16 M2O3 in the unit of structure. The inter-atomic distances reported by him are 2.16-2.20 A. for scandium oxide and 2.34-2.38 A. for yttrium oxide, in good agreement with the radius sums 2.21 A. for Sc+3-0= and 2.33 A. for Y+3-0". 

The oxidation-resistant SiC fiber was prepared from polycarbosilane containing Zr(OC4H9)4 by the same process as that used for the aforementioned tita-nia/silica fiber, except that the calcination was performed in Ar atmosphere at 1400 °C. In this case, the polycarbosilane and Zr(OC4H9)4 were effectively converted into SiC-based bulk ceramic and zirconium oxide (cubic zirconia). Before the conversion, bleed-out of the zirconium compound proceeded effectively. AES depth analysis of the fiber surface showed an increase in the concentration of zirconium towards the surface. This construction was confirmed by the TEM image of the cross-section near the fiber surface. This indicates the direct production of a SiC-based fiber covered with a Zr02 surface layer, which... 

Figure 5.8. Lanthanide Ln203 oxides (cubic cI80-Mn2O3 type, on the left side) and Pb alloys (LnPb3, cubic cP4-type, on the right). The trends of the lattice parameter and of the heat of formation are shown (see the text and notice the characteristic behaviour of Eu and Yb). A schematic representation of the energy difference between the divalent and trivalent states of an ytterbium compound is shown. Apromff represents the promotion energy from di- to trivalent Yb metal, A,//11, and Ar/Ynl are the formation enthalpies of a compound in the two cases in which there is no valence change on passing from the metal to the compound the same valence state (II or III) is maintained.

Figure 5. Time-averaged structure of a protonic defect in perovskite-type oxides (cubic case), showing the eight orientations of the centrai hydroxide ion stabiiized by a hydrogen-bond interaction with the eight next-nearest oxygen neighbors. ...

Cu5FeS4 PENTACOPPER IRON TETRASULFIDE 616 Er203 ERBIUM OXIDE (CUBIC) 660... 

CuFe204 COPPER DIIRON TETRAOXIDE 624 Eu203 EUROPIUM OXIDE (CUBIC) 667... 

FeV204 IRON DIVANADIUM TETRAOXIDE 716 Gd203 GADOLINIUM OXIDE (CUBIC) 758... 

The metal has a bright silvery metallic luster. Neodymium is one of the more reactive rare-earth metals and quickly tarnishes in air, forming an oxide that spalls off and exposes metal to oxidation. The metal, therefore, should be kept under light mineral oil or sealed in a plastic material. Neodymium exists in two allotropic forms, with a transformation from a double hexagonal to a body-centered cubic structure taking place at 863oC. 

Lead zirconate [12060-01 -4] PbZrO, mol wt 346.41, has two colorless crystal stmctures a cubic perovskite form above 230°C (Curie point) and a pseudotetragonal or orthorhombic form below 230°C. It is insoluble in water and aqueous alkaUes, but soluble in strong mineral acids. Lead zirconate is usually prepared by heating together the oxides of lead and zirconium in the proper proportion. It readily forms soHd solutions with other compounds with the ABO stmcture, such as barium zirconate or lead titanate. Mixed lead titanate-zirconates have particularly high piezoelectric properties. They are used in high power acoustic-radiating transducers, hydrophones, and specialty instmments (146). 

Elemental composition, ionic charge, and oxidation state are the dominant considerations in inorganic nomenclature. Coimectivity, ie, which atoms are linked by bonds to which other atoms, has not generally been considered to be important, and indeed, in some types of compounds, such as cluster compounds, it caimot be appHed unambiguously. However, when it is necessary to indicate coimectivity, itaUcized symbols for the connected atoms are used, as in trioxodinitrate(A/,A/), O2N—NO . The nomenclature that has been presented appHes to isolated molecules (or ions). Eor substances in the soHd state, which may have more than one crystal stmcture, with individual connectivities, two devices are used. The name of a mineral that exemplifies a particular crystal stmcture, eg, mtile or perovskite, may be appended. Alternatively, the crystal stmcture symmetry, eg, rhombic or triclinic, may be cited, or the stmcture may be stated in a phrase, eg, face-centered cubic. 

Iron Blocks. Chemically, iron blacks are based on the binary iron oxide, FeOFe2 O3. Although the majority is produced in the cubical form, these can also be produced in acicular form. Most of the black iron oxide pigments contain iron(III) oxide impurities, giving a higher ratio of iron(III) than would be expected from the theoretical formula. 

Properties. Thallium is grayish white, heavy, and soft. When freshly cut, it has a metallic luster that quickly dulls to a bluish gray tinge like that of lead. A heavy oxide cmst forms on the metal surface when in contact with air for several days. The metal has a close-packed hexagonal lattice below 230°C, at which point it is transformed to a body-centered cubic lattice. At high pressures, thallium transforms to a face-centered cubic form. The triple point between the three phases is at 110°C and 3000 MPa (30 kbar). The physical properties of thallium are summarized in Table 1. 

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