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Silicate crystal structure

Several qualitative predictions and interpretations of the relative enrichments of transition metal cations in different coordination sites having octahedral, tetragonal, trigonal and lower symmetries may be made based on the theoretical stabilization energies summarized in table 6.4. The predicted and observed enrichments of transition metal ions in ferromagnesian silicate crystal structures are summarized in table 6.5. [Pg.266]

In earlier chapters, allusions were made to die effects of covalent bonding. For example, covalent interactions were invoked to account for the intensification of absorption bands in crystal field spectra when transition metal ions occupy tetrahedral sites ( 3.7.1) patterns of cation ordering for some transition metal ions in silicate crystal structures imply that covalency influences the intracrystalline (or intersite) partitioning of these cations ( 6.8.4) and, the apparent failure of the Goldschmidt Rules to accurately predict the fractionation of transition elements during magmatic crystallization was attributed to covalent bonding characteristics of these cations ( 8.3.2). [Pg.428]

Keywords Germanium / Zwitterions / X 5 -Silicates / Crystal Structure... [Pg.466]

Keywords Pentacoordinate Silicon / Zwitterionic A, 5/-Silicates / Monocyclic i 5i-Silicates / Crystal Structures... [Pg.456]

Fig. 3.2-1 Schematic representation of the arrangement of the [Si04] tetrahedra in planar silicate crystal structures 1, nesosilicate 2, sorosilicate 3, cyclosilicate 4 and 5, inosilicates 6 and 7, ribbon silicates 8, layered silicate or phyllosilicate... Fig. 3.2-1 Schematic representation of the arrangement of the [Si04] tetrahedra in planar silicate crystal structures 1, nesosilicate 2, sorosilicate 3, cyclosilicate 4 and 5, inosilicates 6 and 7, ribbon silicates 8, layered silicate or phyllosilicate...
Particle shape layered silicate Crystal structure trioctahedral smectite ... [Pg.13]

Ahrens, T.J., Anderson, D.L., and Ringwood, A.E. (1969), Equation of State and Crystal Structures of High-Pressure Phases of Shocked Silicates and Oxides, Rev. Geophys. 7, 667-707. [Pg.110]

A colorless mineral known as corundum (composed of aluminum oxide) is colorless. A red variety of corundum known as ruby, a precious stone, owes its color to impurities of chromium within the crystal structure of corundum. Blue and violet varieties of corundum are classified as sapphires, the blue being the result of iron and titanium impurities, and the violet of vanadium impurities within the corundum crystal structure. Another colorless mineral is beryl (composed of beryllium aluminum silicate) but blue aquamarine, green emerald, and pink morganite, are precious varieties of beryl including different impurities aquamarine includes iron, emerald chromium and vanadium, and morganite manganese. [Pg.53]

In addition to the large number of silicate crystals, the Si04 tetrahedra are the basis of many glasses in which the structure derives from that of the liquid state. These structures have short-range but not long-range order. [Pg.144]

A bar of talc feels like a bar of soap which is why it is often called soapstone. Its exceptional softness (it is the softest of the Mohs minerals) is a direct result of its unusual crystal structure. This consists of sheets of silicate tetrahedra without metal ions between the sheets. Thus the sheets are bonded only by London polarization forces. The latter are particularly weak because silicate tetrahedra have relatively small polarizabilities. [Pg.146]

Talc is a hydrated magnesium silicate, Mg6(Si802o)(OH)4. It is a layerd compound like mica. One layer of its crystal structure is shown schematically in Figure 11.3. Such layers are stacked up like playing cards in real crystals. Notice that the top and bottom of the layer consist of slicate tetrahedra with oxygen... [Pg.146]

The crystal structure of ECS-2 can be described by the stacking of alumino-silicate layers held together by phenylene groups (Fig.l). These layers are composed by aluminum centered tetrahedra bonded to [Si03C] tetrahedra. [Pg.216]

Amperometric cells, sensors using, 22 271 Amperometric measurements, 14 612 Amphetamine, 3 89-90 Amphibole asbestos, 1 803 3 288 crystal structure, 3 297-298 exposure limits, 3 316 fiber morphology, 3 294-295 silicate backbone, 3 296 Amphibole potassium fluorrichterite, glass- ceramics based on, 12 637 Amphiphile-oil-water-electrolyte phase diagram, 16 427-428 Amphiphile-oil-water phase diagrams,... [Pg.53]

Crystal lattice packing, 12 249-250 Crystal lattice vibrations, 14 236 Crystalline adsorbents, 1 586, 589. See also Molecular sieves Zeolites for gas separation, 1 631 properties and applications, l 588t Crystalline alkali silicates, atomic structure of, 22 454-455 Crystalline cellulose, 5 373-379 Crystalline epoxy resins, 10 373-374 Crystalline flake graphite, 12 793 manufacture and processing of, 12 781-784... [Pg.235]

Working first with Polanyi, Weissenberg, and Brill, and later as the leader of the Textile Chemistry Section, Mark successively published papers on the crystal structures of hexamethylenetetramine, pentaerythritol, zinc salts, tin, urea, tin salts, triphenylmethane, bismuth, graphite, sulfur, oxalic acid, acetaldehyde, ammonia, ethane, diborane, carbon dioxide, and some aluminum silicates. Each paper showed his and the laboratory s increasing sophistication in the technique of X-ray diffraction. Their work over the period broadened to include contributions to the theories of atomic and molecular structure and X-ray scattering theory. A number of his papers were particularly notable including his work with Polanyi on the structure of white tin ( 3, 4 ), E. Wigner on the structure of rhombic sulfur (5), and E. Pohland on the low temperature crystal structure of ammonia and carbon dioxide (6, 7). The Mark-Szilard effect, a classical component of X-ray physics, was a result of his collaboration with Leo Szilard (8). And his work with E. A. Hauser (9, 10, 11) on rubber and J. R. [Pg.18]

In the silicate crystal chemistry, compounds such as Mg3Al2Si30i2 are classified within the orthosilicates owing to the isolated Si044+ tetrahedra existing in their structure, and better described by a chemical formula such as Mg3Al2(Si04)3. [Pg.745]

Each of these solid phases can be described in terms of their mineralogy. This classification scheme is based on crystal structure and chemical composition. The most common minerals found in marine sediments are listed in Table 13.2. Most are silicates in which Si and O form a repeating tetrahedral base unit. Other minerals common to marine sediments are carbonates, sulfates, and oxyhydroxides. Less common are the hydrogenous minerals as they form only in restricted settings. These include the evap-orite minerals (halides, borates, and sulfates), hydrothermal minerals (sulfides, oxides, and native elements, such as gold), and phosphorites. [Pg.330]

Bowen s reaction series representing the relationship of igneous silicate mineral composition to crystallization temperature. The plagioclase feldspars represent a continuous series grading from the calcium-rich to sodium-rich to potassium-rich forms. The rest of the minerals constitute a discontinuous series in which distinct crystal structures are characteristic of a particular temperature range under which the magma solidified. [Pg.354]


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See also in sourсe #XX -- [ Pg.169 , Pg.170 ]




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Crystallization silicate

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