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Clay minerals density

Particle size distribution Bulk density Clay mineral type pH... [Pg.1071]

Clay minerals or phyllosilicates are lamellar natural and synthetic materials with high surface area, cation exchange and swelling properties, exfoliation ability, variable surface charge density and hydrophobic/hydrophilic character [85], They are good host structures for intercalation or adsorption of organic molecules and macromolecules, particularly proteins. On the basis of the natural adsorption of proteins by clay minerals and various clay complexes that occurs in soils, many authors have investigated the use of clay and clay-derived materials as matrices for the immobilization of enzymes, either for environmental chemistry purpose or in the chemical and material industries. [Pg.454]

The inductive effect of the carbon chain in the clay phase amounts to (only) 5 to 7 % of the effect in the gas phase. Ammonium cations in the interlamellar region of clay minerals are therefore less hydrated than in equilibrium solution. The free energy of alkylammonium exchange increases with charge density from Laponite (42) < Red Hill montmorillonite (40) < Camp Berteau montmorillonite (41) in line with the smaller interlamellar hydration status of the adsorbed cation at higher charge density. [Pg.260]

Exchange in zeolites of alkali, alkaline earth, transition metal ions and small organic ammonium ions, has been reviewed (111), and in general, the exchange is characterized by small AG values comparable to those found in clay minerals. Althoufft identical selectivity orders for alkali and alkaline earth metal ions are obtained, as in montmorillonite, the opposite variation of AG with charge density is found. [Pg.283]

Some green clay minerals occur as ovoids, probably having formed within fecal pellets or casts of forams. They also occur as films or stains on shells, sand grains, and phosphate nodules. They are finmd in highest density in sediments of the outer continental shelves and slopes where waters are shallow (20 to 700 m) and mildly suboxic. Slow sedimentation rates are necessary to prevent burial as green clays form at very slow rates. A notable example are the green muds found on the Blake Plateau. [Pg.470]

The actual density of clay minerals is 2.7g/cm. but these solids are surrounded by pore waters as they accumulate in the sediments. An average wet density of marine sediments is estimated at 1.6g/cm ... [Pg.526]

Nickel is strongly adsorbed by soil, although to a lesser degree than lead, copper, and zinc (Rai and Zachara 1984). There are many adsorbing species in soil, and many factors affect the extent to which nickel is adsorbed, so the adsorption of nickel by soil is site specific. Soil properties such as texture, bulk density, pH, organic matter, the type and amount of clay minerals, and certain hydroxides influence the retention and release of metals by soil (Richter and Theis 1980). [Pg.186]

The net permanent structural surface charge density, denoted gq and measured in coulombs per square meter (C/m2), is created by isomorphic substitutions in minerals [4]. These substitutions in clay minerals produce significant surface charge only in the 2 1 layer types. In these minerals, Co < 0 invariably because of structural cation substitutions. The relation between gq and the layer charge jc is [3]... [Pg.211]

The intrinsic surface charge density reflects particle charge developed from either isomorphic substitutions or adsorption involving H+ or OH-. A widely used technique for measuring intrinsic surface charge density is the Schofield method. In this method [3], clay mineral particles are reacted with an electrolyte solution (e.g., NaCl) at a given pH value and ionic strength the specific surface excess of the cation and the anion adsorbed from the electrolyte is determined and the value of is calculated with the equation... [Pg.212]

The Poisson-Boltzman (P-B) equation commonly serves as the basis from which electrostatic interactions between suspended clay particles in solution are described ([23], see Sec.II. A. 2). In aqueous environments, both inner and outer-sphere complexes may form, and these complexes along with the intrinsic surface charge density are included in the net particle surface charge density (crp, 4). When clay mineral particles are suspended in water, a diffuse double layer (DDL) of ion charge is structured with an associated volumetric charge density (p ) if av 0. Given that the entire system must remain electrically neutral, ap then must equal — f p dx. In its simplest form, the DDL may be described, with the help of the P-B equation, by the traditional Gouy-Chapman [23-27] model, which describes the inner potential variation as a function of distance from the particle surface [23]. [Pg.230]

FIGURE 1.2 Structure of a hydrated sodium Llano vermiculite determined by X-ray diffraction [5]. The experimental structure amplitudes were assigned phases calculated on the basis of scattering by the atoms of the silicate layers only, and the resulting observed structure factors (Fo values) were used, in conjunction with the calculated structure factors (Fc values), to compute Fo-Fc projections of the electron densities onto the 010 and the 100 faces of the unit cell, shown in the parts (a) and (b), respectively. That the interlayer cations and water molecules are in octahedral coordination accords with these Fourier projections. (Reproduced with kind permission of the Clay Minerals Society, from Slade, P.G., Stone, P.A., and Radoslovich, E.W., Clays Clay Min., 33, 51, 1985.)... [Pg.3]


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