Cation clays and

Calvet, R. (1975) Dielectric properties of montmorillonites saturated by bivalent cations, Clays and Clay Minerals 23, 257-265... 

Mostly focused on cationic clays, and particularly on montmorillonite and hectorite, smectite-type layered silicates and clay-based nanofillers have recently been extended to the family of LDH. Hydrotalcite-like LDH materials are described according to the ideal formula, [M1/ xM"l(OH)2]frl(lra [A H20]inter, where Mn and Mm are metallic cations, A the anions, and intra and inter denote the intralayer and interlayer domain, respectively. The structure consists of brucite-like layers constituted of edge-sharing octahedra. The presence of trivalent cations induces positive charges in the layers that are counterbalanced by interlamellar anions (Scheme 15.16). 

Conductive electrodes based on metal oxide, e.g., indium-tin oxide (TTO), are widely used in electrochemistry as a support for surface modification with the goal to develop sensors with electrochemical transduction or combined spectroscopic and electrochemical responses or electrochemiluminescence. Inorganic thin films can also be prepared from the assembly of two-dimensional layered inorganic solids, such as cationic clays and layered double hydroxides (LDHs, also defined as anionic clays). These materials can be used to preconcentrate species on the basis of ion-exchange reactions and applied to heavy metal determination or for the detection of organic pollutants. 

The choice of catalyst is based primarily on economic effects and product purity requirements. More recentiy, the handling of waste associated with the choice of catalyst has become an important factor in the economic evaluation. Catalysts that produce less waste and more easily handled waste by-products are strongly preferred by alkylphenol producers. Some commonly used catalysts are sulfuric acid, boron trifluoride, aluminum phenoxide, methanesulfonic acid, toluene—xylene sulfonic acid, cationic-exchange resin, acidic clays, and modified zeoHtes. 

The hot-water separation process involves extremely compHcated surface chemistry with interfaces among various combinations of soUds (including both silica sand and alurninosilicate clays), water, bitumen, and air. The control of pH is critical. The preferred range is 8.0—8.5, achievable by use of any of the monovalent bases. Polyvalent cations must be excluded because they tend to flocculate clays and thus raise viscosity of the middlings in the separation cell. 

The methylene blue test can also be used to determine cation exchange capacity of clays and shales. In the test a weighed amount of clay is dispersed into water by a high-speed stirrer. Titration is carried out as for drilling muds, except that hydrogen peroxide is not added. The cation exchange capacity of clays is expressed as milliequivalents of methylene blue per 100 g of clay. 

Two classes of clays are known [3] (i) cationic clays (or clay minerals) that have negatively charged alumino-silicate layers balanced by small cations in the interlayer space (e.g. K-10 montmorillonite) and (ii) anionic clays which have positively charged brucite-type metal hydroxide layers balanced by anions and water molecules located interstitially (e.g. hydrotalcite, Mg6Al2(0H)igC034H20. 

Vaccari A. Clays and Catalysis a Promising Future Appl. Clay Sci. 1999 74161-198 Keywords cationic and anionic clays, catalysis... 

Vaccari (1983,1999) has given a state-of-the-art account of the preparation and catalytic properties of cationic and anionic clays. Some examples of industrial importance have also been reported. Clays exhibit many desirable features, such as low cost, wide range of preparation variables, ease of set-up and wOrk-up, high selectivity, and environmental friendliness. Cationic clays are widespread in nature, whereas anionic clays are rarely found in nature, but they can be synthesized cheaply. Cationic clays are prepared from the minerals but industrial anionic clays are generally synthetic. Smectite clays exhibit both Brpnsted and Lewis acid sites on the edges of the crystals. Hammet s acidity function values are as follows Na -montmorillonite (M), -3 to t- 1.5 NH4VM -3 to 1.5 H M -8.2 to -5.6 acid activated clay less than -8.2. Laporte also has a synthetic version of cationic clays, Laponite. The acid... 

Carboxymethylcellulose, polyethylene glycol Combination of a cellulose ether with clay Amide-modified carboxyl-containing polysaccharide Sodium aluminate and magnesium oxide Thermally stable hydroxyethylcellulose 30% ammonium or sodium thiosulfate and 20% hydroxyethylcellulose (HEC) Acrylic acid copolymer and oxyalkylene with hydrophobic group Copolymers acrylamide-acrylate and vinyl sulfonate-vinylamide Cationic polygalactomannans and anionic xanthan gum Copolymer from vinyl urethanes and acrylic acid or alkyl acrylates 2-Nitroalkyl ether-modified starch Polymer of glucuronic acid... 

Flocculants cause colloidal clay particles to coagulate thus promoting separation from the drilling fluid which has been circulated down the wellbore and returned to the surface. The treated fluid may then be pumped back down the well bore. Sodium chloride, hydrated lime, gypsum, sodium tetraphosphate, polyacrylamide, poly(acrylamide-co-acrylic acid), cationic polyacrylamides, and poly(ethylene oxide) have been used commercially. 

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. 

The dispersion and solid-state ion exchange of ZnCl2 on to the surface of NaY zeolite by use of microwave irradiation [17] and modification of the surface of active carbon as catalyst support by means of microwave induced treatment have also been reported [18]. The ion-exchange reactions of both cationic (montmorillonites) and anionic clays (layered double hydroxides) were greatly accelerated under conditions of microwave heating compared with other techniques currently available [19.]... 

Churchman GJ (2002) Formation of complexes between bentonite and different cationic polyelectrolytes and their use as sorbents for non-ionic and anionic pollutants. Appl Clay Sci 21 177-189... 

Jaynes WF, Vance GF (1999) Sorption of benzene, toluene, ethylbenzene and xylene (BTEX) compounds by hectorite clays exchanged with aromatic organic cations. Clays Clay Miner 47 358-365 Johnston CT, De Oliveira MF, Teppen BJ, Sheng G, Boyd SA (2001) Spectroscopic study of nitroaromatic-smectite sorption mechanisms. Environ Sci Technol 35 4767-4772... 

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