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Octahedral sheet

The stacking of the tetrahedral and octahedral sheets in the chrysotile structure has been shown to yield three types of chrysotile fibers (10) ... [Pg.348]

Clay minerals that are composed of two tetrahedral layers and one octahedral layer are referred to as 2 1 clay minerals or TOT minerals. The apical oxygens of the two tetrahedral sheets project into the octahedral sheet. The 2 1 stmcture has a basal spacing (nominal thickness) of 1.0 nm (10 E). Pyrophjlhte [12269-78-2] Al2Si40 Q(0H)2, is the dioctahedral mineral, ie, AF" in the octahedral sites, and talc [14807-96-6], Mg3Si402Q(0H)2, is the trioctahedral, ie, in the octahedral sites. Both these minerals are essentially free of substitution in the octahedral site and therefore do not have a net... [Pg.195]

Palygorskite and sepioHte minerals are 2 1 layered phyUosiHcates that differ from the above mentioned clays because the octahedral sheets have significant intracrystalline void space caused by discontinuous octahedral layers. The basal tetrahedral unit is connected to an adjacent inverted basal tetrahedral creating a void space or channel. Charge deficits are balanced by hydrated cations in the intracrystalline space. [Pg.195]

We have done our experiments with hectorite, which is a 2 1 smectite that develops negative layer charge by substitution of Li for Mg in the octahedral sheet.Samples were prepared by multiple exchange in 1.0 and 0.1 M CsCl solutions until essentially complete Cs-exchange was reached (97% of the interlayer cations). Temperature dependent data are essential to interpret the results, because there is rapid exchange of Cs among different interlayer sites at room temperature (RT). [Pg.158]

Layer-silicate structure, as in other silicate minerals, is dominated by the strong Si-O bond, which accounts for the relative insolubility of these minerals. Other elements involved in the building of layer silicates are Al, Mg, or Fe coordinated with O and OH. The spatial arrangement of Si and these metals with O and OH results in the formation of tetrahedral and octahedral sheets (see Fig. 8-2). The combination of the tetrahedral and octahedral sheets in different groupings, and in conjunction with different metal oxide sheets, generates a number of different layer silicate clays (see Table 8-1). [Pg.166]

The brownmillerite structure type can be described as a sequence. .. OTOT... where O stands for the octahedral sheet and T the tetrahedral sheet. A number of other phases closely related to this structure have been characterized, including Ca2LaFe308, with a stacking sequence. .. OOTOOT... and Ca4Ti2Fe20i 1 and... [Pg.190]

Figure 3.4. Two types of isomorphous substitution. The middle structures are two-dimensional representations of clay without isomorphous substitution. On the left is an isomorphous substitution of Mg for A1 in the aluminum octahedral sheet. On the right is isomorphous A1 substitution for Si in the silicon tetrahedral sheet. Clays are three-dimensional and -OH on the surface may be protonated or deprotonated depending on the pH of the surrounding soil solution. There will be additional water molecules and ions between many clay structures. Note that clay structures are three-dimensional and these representations are not intended to accurately represent the three-dimensional nature nor the actual bond lengths also, the brackets are not intended to represent crystal unit cells. Figure 3.4. Two types of isomorphous substitution. The middle structures are two-dimensional representations of clay without isomorphous substitution. On the left is an isomorphous substitution of Mg for A1 in the aluminum octahedral sheet. On the right is isomorphous A1 substitution for Si in the silicon tetrahedral sheet. Clays are three-dimensional and -OH on the surface may be protonated or deprotonated depending on the pH of the surrounding soil solution. There will be additional water molecules and ions between many clay structures. Note that clay structures are three-dimensional and these representations are not intended to accurately represent the three-dimensional nature nor the actual bond lengths also, the brackets are not intended to represent crystal unit cells.
Figure 3.11. Upper diagram micelle of sodium octanoate in water lower diagram micelle of 2 1 clay (the center gray layer is an aluminum octahedral sheet the upper and lower are silicon tetrahedral sheets). Figure 3.11. Upper diagram micelle of sodium octanoate in water lower diagram micelle of 2 1 clay (the center gray layer is an aluminum octahedral sheet the upper and lower are silicon tetrahedral sheets).
Two cases of isomorphic substitution can be distinguished In the tetrahedral sheet, or in the octahedral sheet (Sposito, 1984). [Pg.62]

Kaolinite particles. Typically about 50 unit layers of hexagonal plates are stacked irregularly and interconnected through H-bonding between the OH-groups of the octahedral sheet and the oxygens of the tetrahedral sheet (Fig. 3.9) (Sposito, 1989)... [Pg.245]

The layer silicates comprise tetrahedral sheets of silica and octahedral sheets of aluminium and magnesium hydroxide, with varying amounts of the Si, Al and Mg replaced by cations of lower valence giving the lattice a net negative charge. Two basic combinations occur 1 tetrahedral sheet with 1 octahedral (e.g. kaoUnite, halloysite), and 2 tetrahedral with 1 octahedral (e.g. smectite, vermiculite, illite). [Pg.65]

In neutral soils with smectite or vermiculite in the clay fractions, the changes in redox and bases status following soil flooding may cause synthesis of materials similar to smectite with Fe + in the octahedral sheet. Other cations, e.g. Zn +, may also become entrapped. [Pg.74]

Kaolinite crystals in the subsurface are submicron sized and exhibit a platelike morphology. They usually are found mixed with other layered structured minerals. In a comprehensive review, Dixon (1989) summarizes the structural properties of kaohnite. This mineral is composed of tetrahedral and octahedral sheets constituting a 0.7 mn layer in a triclinic unit cell. Two thirds of the octahedral positions are occupied by Al the tetrahedral positions are occupied by Si and Al, which are... [Pg.7]

Micas are classified according to the charge of the mixed layer per formula unit. This depends on the diadochy level of AF (or Fe or, more rarely, Be ) with in tetrahedral groups, and on the charge (and occupancy) of the cation in the intermediate octahedral sheet. [Pg.321]


See other pages where Octahedral sheet is mentioned: [Pg.284]    [Pg.285]    [Pg.195]    [Pg.196]    [Pg.196]    [Pg.199]    [Pg.167]    [Pg.29]    [Pg.30]    [Pg.29]    [Pg.475]    [Pg.58]    [Pg.14]    [Pg.17]    [Pg.58]    [Pg.242]    [Pg.419]    [Pg.146]    [Pg.147]    [Pg.148]    [Pg.64]    [Pg.68]    [Pg.62]    [Pg.62]    [Pg.45]    [Pg.314]    [Pg.504]    [Pg.49]    [Pg.62]    [Pg.443]    [Pg.65]    [Pg.7]    [Pg.9]    [Pg.10]    [Pg.266]    [Pg.321]   
See also in sourсe #XX -- [ Pg.47 ]




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