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Sodium smectite

E. S. Boek and M. Sprik (2003) Ab initio molecular dynamics study of the hydration of a sodium smectite clay. J. Phys. Chem. B 107, p. 3251... [Pg.275]

Smectites, by virtue of their large surface area, are particularly sensitive to the exchangeable cation type. In nature, the most common cations are Ca and Na. Calcium ions reduce bound water layer thickness and provide some deformation resistance by cross-linking clay platelet surfaces. Sodium smectite, on the other hand, has the highest affinity for water of any common phyllosilicate, and is therefore used in water-based muds (WBM) to build viscosity and to suspend fine-grained materials used to increase the mud weight. The most geochemically sensitive shales are almost invariably smectitic with saline pore fluids. [Pg.574]

Borgesson, L., Hoekmark, H. Karnland, O. 1988. Rheological properties of sodium smectite clay. Swedish Nuclear Fuel and Waste Management Co. (SKB) Technical Report TR 88-30, SKB, Stockholm, Sweden. [Pg.66]

Unlike vermiculite, the smectite crystal structure accommodates additional interlaminar water layers, due at least in part to its lower counterion density. This allows for hydraulic delamination. On immersion in water, sodium smectites incorporate enough additional water layers to overcome weak... [Pg.15]

Aromatic polycarbonates are currently manufactured either by the interfacial polycondensation of the sodium salt of diphenols such as bisphenol A with phosgene (Reaction 1, Scheme 22) or by transesterification of diphenyl carbonate (DPC) with diphenols in the presence of homogeneous catalysts (Reaction 2, Scheme 22). DPC is made by the oxidative carbonylation of dimethyl carbonate. If DPC can be made from cyclic carbonates by transesterification with solid catalysts, then an environmentally friendlier route to polycarbonates using C02 (instead of COCl2/CO) can be established. Transesterifications are catalyzed by a variety of materials K2C03, KOH, Mg-containing smectites, and oxides supported on silica (250). Recently, Ma et al. (251) reported the transesterification of dimethyl oxalate with phenol catalyzed by Sn-TS-1 samples calcined at various temperatures. The activity was related to the weak Lewis acidity of Sn-TS-1 (251). [Pg.130]

The size distribution of the kaolinite is quite variable and again the Kingston sample differed in that most of the kaolinite has sodium associated with it and could therefore be considered a smectite rather than kaolinite. Marcasite is commonly present as a replacement of original coal particles. The gypsum is present mainly in the -20 ym size range. Overall the mineral matter content of the lignites is of the order of 5%-10% (i.e. a medium distribution density). [Pg.28]

The results of this reaction are precipitation of smectite clay and release of silicic acid, sodium ions, and bicarbonate ions to solution. The actual dissolution reaction is significantly more complex than indicated here, as discussed in Section 2.4. [Pg.463]

Smectite-type materials were synthesized with a hydrothermal method [5]. The aqueous solution of sodium silicate (Si02 / NajO= 3.22) and sodium hydroxide was mixed with the aqueous solution of metal chloride to precipitate Si-M (M divalent metal cation, Si M = 8 6) hydroxides. The precipitation pH of Si-M hydroxide was controlled by changing the molar ratio of sodium hydroxide to sodium silicate. After separating and washing of Si-M hydroxide, slurries were prepared from Si-M hydroxide and water. The Si-M slurries were treated hydrothermally in an autoclave at 473 K under autogaseous water vapor pressure for 2 h. The resultant samples were dried at 353 K then we obtained smectite samples. The smectite-type materials are denoted by the divalent species in octahedral sheets and BET surface area, e.g., Ni-481 for the Ni2+ substituted smectite-type material with a surface area of 481 m2g. ... [Pg.436]

Table 1 shows the properties of smectite-type materials prepared. Smectite materials prepared at lower pH had fewer sodium ions, higher surface areas, and larger pore volumes for a series of samples containing the same divalent cation species (nickel and cobalt) in the octahedral sheet. The adsorption of methylene blue on all the synthetic smectites shows that the smectite fragments are negatively charged. The Si M ratios of synthetic smectites were about 8 6, indicating that most of divalent cations exist in octahedral layers and small amount of divalent cations would exist as hydroxide or oxide cluster in smectite materials. However, the amounts of the hydroxide or oxide cluster were small, because only smectite structures were observed in XRD patterns and EXAFS Fourier transforms of synthetic smectites calcined at 873 K. [Pg.436]

Evidences for electron transfer from surface tg bulk. According to the nature of the clay, variable amounts of Fe are present in the lattice. Glauconite, which is an iron rich member of the dioctahedral smectite family, reacts at pH 7 with sodium... [Pg.367]


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