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Cubic closed packed

Spinel Ferrites. In spinel ferrites having the composition where A and B are metals, cubic close-packed oxygen ions leave two kinds of... [Pg.188]

Titanium Trichloride. Titanium trichloride [7705-07-9] exists in four different soHd polymorphs that have been much studied because of the importance of TiCl as a catalyst for the stereospecific polymerization of olefins (120,124). The a-, y-, and 5-forms are all violet and have close-packed layers of chlorines. The titaniums occupy the octahedral interstices between the layers. The three forms differ in the arrangement of the titaniums among the available octahedral sites. In a-TiCl, the chlorine sheets are hexagonaHy close-packed in y-TiCl, they are cubic close-packed. The brown P-form does not have a layer stmcture but, instead, consists of linear strands of titaniums, where each titanium is coordinated by three chlorines that act as a bridge to the next Ti The stmctural parameters are as follows ... [Pg.129]

The a-rhombohedral form of boron has the simplest crystal stmcture with slightly deformed cubic close packing. At 1200°C a-rhombohedral boron degrades, and at 1500°C converts to P-rhombohedral boron, which is the most thermodynamically stable form. The unit cell has 104 boron atoms, a central B 2 icosahedron, and 12 pentagonal pyramids of boron atom directed outward. Twenty additional boron atoms complete a complex coordination (2). [Pg.184]

When Li metal is cold-worked it transforms from body-centred cubic to cubic close-packed in which each atom is surrounded by 12 others in twinned cuboctahedral coordination below 78 K the stable crystalline modification is hexagonal dose-packed in which each lithium atom has 12 nearest neighbours in the form of a cuboctahedron. This very high coordination... [Pg.93]

Figure 29.1 Crystal structures of ZnS. (a) Zinc blende, consisting of two, interpenetrating, cep lattices of Zn and S atoms displaced with respect to each other so that the atoms of each achieve 4-coordination (Zn-S = 235 pm) by occupying tetrahedral sites of the other lattice. The face-centred cube, characteristic of the cep lattice, can be seen — in this case composed of S atoms, but an extended diagram would reveal the same arrangement of Zn atoms. Note that if all the atoms of this structure were C, the structure would be that of diamond (p. 275). (b) Wurtzite. As with zinc blende, tetrahedral coordination of both Zn and S is achieved (Zn-S = 236 pm) but this time the interpenetrating lattices are hexagonal, rather than cubic, close-packed. Figure 29.1 Crystal structures of ZnS. (a) Zinc blende, consisting of two, interpenetrating, cep lattices of Zn and S atoms displaced with respect to each other so that the atoms of each achieve 4-coordination (Zn-S = 235 pm) by occupying tetrahedral sites of the other lattice. The face-centred cube, characteristic of the cep lattice, can be seen — in this case composed of S atoms, but an extended diagram would reveal the same arrangement of Zn atoms. Note that if all the atoms of this structure were C, the structure would be that of diamond (p. 275). (b) Wurtzite. As with zinc blende, tetrahedral coordination of both Zn and S is achieved (Zn-S = 236 pm) but this time the interpenetrating lattices are hexagonal, rather than cubic, close-packed.
Ni, Mn, V). In the ideal layered LiM02 structure, the Li+ and the M3+ ions occupy octahedral sites in alternate layers between cubic close packed oxygen layers (Fig. 5). [Pg.300]

MHX-Ni batteries 219 crystallography 365 cubic close packing 47 cubic packed arrays 293 curing, lead oxides 167... [Pg.607]

The surface of a single crystal of nickel, showing the regularity of its cubic close-packed structure. [Pg.311]

FIGURE 5.28 A fragment ot the structure constructed as described in Fig. 5.27. This fragment shows the origin of the names "cubic close-packed" or "face-centered cubic" for this arrangement. The layers A, B, and C can be seen along the diagonals of the faces of the cube and are indicated by the different colors of the atoms. [Pg.317]

The best way to determine the type of unit cell adopted by a metal is x-ray diffraction, which gives a characteristic diffraction pattern for each type of unit cell (see Major Technique 3 following his chapter). However, a simpler procedure that can be used to distinguish between close-packed and other structures is to measure the density of the metal we then calculate the densities of the candidate unit cells and decide which structure accounts for the observed density. Density is an intensive property, which means that it does not depend on the size of the sample (Section A). Therefore, it is the same for a unit cell and a bulk sample. Hexagonal and cubic close packing cannot be distinguished in this way, because they have the same coordination numbers and therefore the same densities (for a given element). [Pg.319]


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