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Structure tetragonal

When a copper(II) salt dissolves in water, the complex aquo-ion [Cu(H2p)6P is formed this has a distorted octahedral (tetragonal) structure, with four near water molecules in a square plane around the copper and two far water molecules, one above and one below this plane. Addition of excess ammonia replaces only the four planar water molecules, to give the deep blue complex [Cu(NH3)4(H20)2] (often written as [Cu(NHj)4] for simplicity). TTo obtain [Cu(NH3)6], water must be absent, and an anhydrous copper(II) salt must be treated with liquid ammonia. [Pg.413]

Fig. 2. Structures for the solid (a) fee Cco, (b) fee MCco, (c) fee M2C60 (d) fee MsCeo, (e) hypothetical bee Ceo, (0 bet M4C60, and two structures for MeCeo (g) bee MeCeo for (M= K, Rb, Cs), and (h) fee MeCeo which is appropriate for M = Na, using the notation of Ref [42]. The notation fee, bee, and bet refer, respectively, to face centered cubic, body centered cubic, and body centered tetragonal structures. The large spheres denote Ceo molecules and the small spheres denote alkali metal ions. For fee M3C60, which has four Ceo molecules per cubic unit cell, the M atoms can either be on octahedral or tetrahedral symmetry sites. Undoped solid Ceo also exhibits the fee crystal structure, but in this case all tetrahedral and octahedral sites are unoccupied. For (g) bcc MeCeo all the M atoms are on distorted tetrahedral sites. For (f) bet M4Ceo, the dopant is also found on distorted tetrahedral sites. For (c) pertaining to small alkali metal ions such as Na, only the tetrahedral sites are occupied. For (h) we see that four Na ions can occupy an octahedral site of this fee lattice. Fig. 2. Structures for the solid (a) fee Cco, (b) fee MCco, (c) fee M2C60 (d) fee MsCeo, (e) hypothetical bee Ceo, (0 bet M4C60, and two structures for MeCeo (g) bee MeCeo for (M= K, Rb, Cs), and (h) fee MeCeo which is appropriate for M = Na, using the notation of Ref [42]. The notation fee, bee, and bet refer, respectively, to face centered cubic, body centered cubic, and body centered tetragonal structures. The large spheres denote Ceo molecules and the small spheres denote alkali metal ions. For fee M3C60, which has four Ceo molecules per cubic unit cell, the M atoms can either be on octahedral or tetrahedral symmetry sites. Undoped solid Ceo also exhibits the fee crystal structure, but in this case all tetrahedral and octahedral sites are unoccupied. For (g) bcc MeCeo all the M atoms are on distorted tetrahedral sites. For (f) bet M4Ceo, the dopant is also found on distorted tetrahedral sites. For (c) pertaining to small alkali metal ions such as Na, only the tetrahedral sites are occupied. For (h) we see that four Na ions can occupy an octahedral site of this fee lattice.
The structure formation in an ER fluid was simulated [99]. The characteristic parameter is the ratio of the Brownian force to the dipolar force. Over a wide range of this ratio there is rapid chain formation followed by aggregation of chains into thick columns with a body-centered tetragonal structure observed. Above a threshold of the intensity of an external ahgn-ing field, condensation of the particles happens [100]. This effect has also been studied for MR fluids [101]. The rheological behavior of ER fluids [102] depends on the structure formed chainlike, shear-string, or liquid. Coexistence in dipolar fluids in a field [103], for a Stockmayer fluid in an applied field [104], and the structure of soft-sphere dipolar fluids were investigated [105], and ferroelectric phases were found [106]. An island of vapor-liquid coexistence was found for dipolar hard spherocylinders [107]. It exists between a phase where the particles form chains of dipoles in a nose-to-tail... [Pg.764]

Phase equilibria in Ti-H alloys are sensitive to pressure. A new phase appears in near-eutectoid alloys at P > 20 kbar with a tetragonal structure and hydrogen re-distributed from tetra- to octahedral interstices. [Pg.436]

Finally, at even lower transformation temperatures, a completely new reaction occurs. Austenite transforms to a new metastable phase called martensite, which is a supersaturated solid solution of carbon in iron and which has a body-centred tetragonal crystal structure. Furthermore, the mechanism of the transformation of austenite to martensite is fundamentally different from that of the formation of pearlite or bainite in particular martensitic transformations do not involve diffusion and are accordingly said to be diffusionless. Martensite is formed from austenite by the slight rearrangement of iron atoms required to transform the f.c.c. crystal structure into the body-centred tetragonal structure the distances involved are considerably less than the interatomic distances. A further characteristic of the martensitic transformation is that it is predominantly athermal, as opposed to the isothermal transformation of austenite to pearlite or bainite. In other words, at a temperature midway between (the temperature at which martensite starts to form) and m, (the temperature at which martensite... [Pg.1283]

The Rutile Structure.—A large number of compounds MX crystallize with the tetragonal structure of rutile, TiCfe. In this structure the position of the ion X is fixed only by the determination of a variable parameter by means of the intensity of reflection of x-rays from various crystal planes. In accordance with the discussion in a following section, we shall assume the parameter to have the value which causes the distances between X and the three ions M surrounding it to be constant. With this requirement the inter-atomic distance R and the edges a and c of the unit of structure are related by the equation R = (a/4 /2) [2 + (c/o)2]. In this way the inter-atomic distances in Table XII are obtained. In the case of magnesium fluoride the agreement is satisfactory. [Pg.269]

It is probable that on heating NH HF rotation2) of the NH4 ions is induced, with an accompanying gradual transition to a tetragonal structure with a = b, w = u, v = 0, and z =, or a discontinuous transition to the KHF2 structure (provided that fusion or sublimation does not occur below the transition temperature). [Pg.428]

There are two important titanium aluminides Tig A1 which has a hexagonal structure with a density of 4.20 g/cm and a melting point of 1600°C and Ti A1 which has a tetragonal structure with a density of 3.91 g/cm and a melting point of 1445°C. As do all aluminides, they have excellent high temperature oxidation resistance owing to the formation of a thin alumina layer on the surface. They have potential applications in aerospace structures. [Pg.176]

Figure 3. Relation between the orthorhombic structure types of CrB and UBC (projected along [100]) as well as between the tetragonal structure types of a-MoB and ThBC (projected along [100]). Boron atoms are at the centers of trigonal metal prisms, carbon atoms at the centers of MjB-Oj,. The numbers given indicate the heights in projection. Figure 3. Relation between the orthorhombic structure types of CrB and UBC (projected along [100]) as well as between the tetragonal structure types of a-MoB and ThBC (projected along [100]). Boron atoms are at the centers of trigonal metal prisms, carbon atoms at the centers of MjB-Oj,. The numbers given indicate the heights in projection.
There are three crystal structures of titanium dioxide rutile, anatase, and brookite. The most active phase is rutile, which has a tetragonal structure [133], as shown in Figure 8.5 [134],... [Pg.227]

Four solid oxide electrolyte systems have been studied in detail and used as oxygen sensors. These are based on the oxides zirconia, thoria, ceria and bismuth oxide. In all of these oxides a high oxide ion conductivity could be obtained by the dissolution of aliovalent cations, accompanied by the introduction of oxide ion vacancies. The addition of CaO or Y2O3 to zirconia not only increases the electrical conductivity, but also stabilizes the fluorite structure, which is unstable with respect to the tetragonal structure at temperatures below 1660 K. The tetragonal structure transforms to the low temperature monoclinic structure below about 1400 K and it is because of this transformation that the pure oxide is mechanically unstable, and usually shatters on cooling. The addition of CaO stabilizes the fluorite structure at all temperatures, and because this removes the mechanical instability the material is described as stabilized zirconia (Figure 7.2). [Pg.239]

Tetragonal structure, of ferroelectric crystals, 11 95, 96 Tetragonal symmetry, 8 114t Tetragonal zirconia polycrystals, 5 571 Tetrahedral... [Pg.933]

The results of the analysis of the intermetallic tetragonal structure types have also been reported and described by Daams and Villars (1997) 404 structure types were analysed. The analysis showed that 294 (clearly intermetallic and correctly refined) were possible with 4264 compounds and 17157 point sets. In this case too it was observed that a small group (23) of atomic environments is greatly preferred. The 23 AET most frequently occurring in the 294 tetragonal structure types are reported in the following list (to be compared with those previously reported for the other systems) ... [Pg.135]


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Tetragonal

Tetragonality

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