Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Aluminosilicates reactions

Several porosity-destroying reactions also characterize this zone. For example, late ferroan carbonate cements are potential reaction products in this zone, and may significantly occlude porosity (Boles 1978). Also, there is a wide variety of aluminosilicate reaction products (e.g., kaolinite, illite, chlorite, and quartz) that can form in this zone as a result of aluminosilicate dissolution. The imbalance between porosity-enhancing or-preserving reac-... [Pg.404]

Boles and Franks 1979). However, it is our position that although these relatively slow aluminosilicate reactions contribute to the alkalinity, they do not buffer the alkalinity until all relatively fast-reacting minerals such as carbonates are eliminated from the fluid/rock system. It is the weak acids and bases (dominately carboxylic acid anions, HCO3, and HS ) in formation waters, coupled with rapidly reacting minerals, such as the carbonate minerals, that buffer formation water pH. [Pg.407]

Sodium alumiaate is widely used in the preparation of alumina-based catalysts. Aluminosilicate [1327-36-2] can be prepared by impregnating siHca gel with alumiaa obtained from sodium alumiaate and aluminum sulfate (41,42). Reaction of sodium alumiaate with siHca or siHcates has produced porous crystalline alumiaosiHcates which are useful as adsorbents and catalyst support materials, ie, molecular sieves (qv) (43,44). [Pg.140]

Typical conditions for the disproportionation reaction are 450-530°C and 20 atmospheres. A mixture of C0O-M0O3 on aluminosilicates/alumina catalysts can he used. Conversions of approximately 40% are normally used to avoid more side reactions and faster catalyst deactivation. The equilihrium constants for this reaction are not significantly changed hy shifting from liquid to vapor phase or hy large temperature changes. [Pg.285]

Microporous catalysts are heterogeneous catalysts used in catalytic converters and for many other specialized applications, because of their very large surface areas and reaction specificity. Zeolites, for example, are microporous aluminosilicates (see Section 14.19) with three-dimensional structures riddled with hexagonal channels connected by tunnels (Fig. 13.38). The enclosed nature of the active sites in zeolites gives them a special advantage over other heterogeneous catalysts, because an intermediate can be held in place inside the channels until the products form. Moreover, the channels allow products to grow only to a particular size. [Pg.687]

Overall, weathering controls the chemistry of material that is transported into the sediment and that which stays behind in the soil. As an example, consider a general weathering reaction for an aluminosilicate (Stumm and Morgan, 1995) ... [Pg.164]

An example of aluminosilicate weathering is the reaction of the feldspar albite to a montmor-illonite-type mineral... [Pg.298]

The intercalates of sheet aluminosilicates (clays) and of graphite are demonstrated to be efficient catalysts for a variety of reactions, and results obtained using several analytical techniques, including magic angle spinning KMR, are presented. For the clay family,... [Pg.472]

This i>aper describes two broad types of intercalation conpomds which are based on graphite on the one hand and sheet aluminosilicate (clay) hosts on the other. Taken together these provide a rich veiriety of examples of heterogeneously catalysed reactions. Appropriately cation exchanged clays, for example, act as efficient catalysts for a number of commercially important proton catalysed reactions (10-13) (see Table I). Graphite intercalates, whilst also capable of... [Pg.472]

Thus an acid-base reaction involves the transfer of an oxide ion (compared with the transfer of a proton in the Bronsted theory) and the theory is particularly applicable in considering acid-base relationships in oxide, silicate and aluminosilicate glasses. However, we shall find that it is subsumed within the Lewis definition. [Pg.17]

From this discussion it can be seen that there is no ideal acid-base theory for AB cements and a pragmatic approach has to be adopted. Since the matrix is a salt, an AB cement can be defined quite simply as the product of the reaction of a powder and liquid component to yield a salt-like gel. The Bronsted-Lowry theory suffices to define all the bases and the protonic acids, and the Lewis theory to define the aprotic acids. The subject of acid-base balance in aluminosilicate glasses is covered by the Lux-Flood theory. [Pg.20]

The polyelectrolyte cements are modern materials that have adhesive properties and are formed by the cement-forming reaction between a poly(alkenoic acid), typically poly(acrylic acid), PAA, in concentrated aqueous solution, and a cation-releasing base. The base may be a metal oxide, in particular zinc oxide, a silicate mineral or an aluminosilicate glass. The presence of a polyacid in these cements gives them the valuable property of adhesion. The structures of some poly(alkenoic acid)s are shown in Figure 5.1. [Pg.90]

An equally simple chemical study was carried out on phytic acid-aluminosilicate cements (Prosser et al., 1983). Phytic acid, myo-inositol hexakis(dihydrogen phosphate), is a naturally occurring substance found in seeds, and it is a stronger acid than phosphoric acid. Cements were prepared using aqueous solutions of phytic acid, concentrated to 50 wt%, and with 5 wt % zinc dissolved in the acid to moderate the rate of reaction with the glass powder. Discs of cement were prepared and these were... [Pg.360]

Aldol condensation reactions have also been conducted. A good example is provided by Climent et al. (1998) for making a-n-amyl cinnamaldehyde (Jasmin aldehyde) by condensing benzaldehyde with n-heptaldehyde, in the presence of mesoporous MCM-41 aluminosilicates. Mesoporous silica-aluminas with a narrow range of pore diameter such as MCM-41 also... [Pg.153]

By using 10 mol% of 51, MS4A, and t-BuSH, the desired product 52 was obtained in up to 98% ee in 80% yield. A complementary role by two metals (Ga and Li) in activating and positioning both of the substrates has been proposed. The MS4A (sodium aluminosilicate) accelerated the reaction however, the actual role of this additive was not clearly defined, although the possibilty that MS4A delivers Na ions was pointed out. Tomioka et al. reported the asymmetric Michael addition of an aromatic thiol to a,P-unsaturated esters in the presence of 8 mol% of 53 to provide 54 in up to 97% ee in 99% yield (Eq. 7.40) [47]. [Pg.232]

Materials formed by acid-base reactions between calcium aluminate compounds and phosphate-containing solutions yield high-strength, low-permeability, C02-resistant cements when cured in hydrothermal environments. The addition of hollow aluminosilicate microspheres to the uncured matrix constituents yields slurries with densities as low as approximately 1200 kg/m, which cure to produce materials with properties meeting the criteria for well cementing. These formulations also exhibit low rates of carbona-tion. The cementing formulations are pumpable at temperatures up to 150° C. [Pg.137]

Formerly derived from the natural mineral lapis lazuli, ultramarine blue pigments have, for more than a century, been manufactured synthetically. The materials used in the manufacture of ultramarines are china clay (a hydrated aluminosilicate), sodium carbonate, silica, sulfur and a carbonaceous reducing material such as coal tar pitch. For the manufacture of the blue pigments, the blend of ingredients is heated to a temperature of 750 800 °C over a period of 50-100 h, and the reaction... [Pg.157]

The migration of heavy metals into mineral lattices is very slow. Ahnstrom and Parker (2001) observed the slow migration of luCd into the residual fraction in arid soils with a weeks-to-years reaction half-time. Theoretically, the residual fraction is comprised of very refractory Cd bound in the lattices of aluminosilicate minerals. Lattice diffusion, a process necessary for isotopic exchange, can require years. [Pg.146]

MCM-22 zeolite (IZA code MWW) presents a novel and original structure which is composed of two independent pore systems a 2-dimensional, sinusoidal, 10-ring intralayer channels system and an interlayer system with 12-ring supercages, accessible through 10-ring apertures [1], This unique pore structure of the aluminosilicate MCM-22 zeolites makes them interesting catalysts for a wide variety of acid-catalyzed reactions, e.g. alkylation of aromatics [2],... [Pg.185]


See other pages where Aluminosilicates reactions is mentioned: [Pg.14]    [Pg.2708]    [Pg.87]    [Pg.424]    [Pg.234]    [Pg.389]    [Pg.415]    [Pg.14]    [Pg.2708]    [Pg.87]    [Pg.424]    [Pg.234]    [Pg.389]    [Pg.415]    [Pg.2765]    [Pg.316]    [Pg.193]    [Pg.409]    [Pg.383]    [Pg.255]    [Pg.971]    [Pg.1028]    [Pg.2]    [Pg.41]    [Pg.145]    [Pg.263]    [Pg.95]    [Pg.251]    [Pg.252]    [Pg.253]    [Pg.86]    [Pg.260]    [Pg.202]    [Pg.432]    [Pg.448]    [Pg.453]    [Pg.469]    [Pg.41]   
See also in sourсe #XX -- [ Pg.404 , Pg.407 ]




SEARCH



Aluminosilicate

© 2024 chempedia.info