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Addition Hydration

Addition of water to unsaturated hydrocarbons (hydration) and the related addition of alcohols are important processes from both practical and chemical points of view. Alcohols and ethers are manufactured in industry by the addition of water and alcohols to alkenes. Hydration of acetylene to produce acetaldehyde, a once important process, has lost its practical importance. [Pg.284]


PRINCIPLES OF NUCLEOPHILIC ADDITION HYDRATION OF ALDEHYDES AND KETONES... [Pg.712]

Principles of Nucleophilic Addition Hydration of Aldehydes and Ketones... [Pg.713]

Precipitation of a hydrated titanium oxide by mixing aqueous solutions of titanium chloride with alkaU forms the precipitation seeds, which are used to initiate precipitation in the Mecklenburg (50) variant of the sulfate process for the production of pigmentary titanium dioxide. Hydrolysis of aqueous solutions of titanium chloride is also used for the preparation of high purity (>99.999%) titanium dioxide for electroceramic appHcations (see Ceramics). In addition, hydrated titanium dioxide is used as a pure starting material for the manufacture of other titanium compounds. [Pg.120]

Very few data are available concerning the stereochemistry of these additions. Hydration of 1,2-dimethylcyclohexene was found to be nonstereoselective.27 In contrast, predominant or exclusive exo-syn addition was shown to take place in the reaction of 2,3-dideuteronorbomene with water and alcohols 28... [Pg.286]

In addition to the three known natural gas hydrates, several other hydrate structures exist. Dyadin et al. (1991) found four hydrate structures and Jeffrey (1984) proposed five additional hydrate structures. These structures have yet to be confirmed in natural gas systems, although new hydrate structures have been identified using x-ray diffraction such as a tetragonal structure for bromine (Udachin et al., 1997b), a trigonal structure for dimethyl ether (Udachin et al., 2001a),... [Pg.347]

In ocean drilling, hydrated sediment cores are often obtained. Because the cores frequently traverse warm waters for periods of about 1 h, hydrated cores dissociate and release gas, to yield higher pressures. When core liners are retrieved on the deck of a drilling vessel, frequently the warm weather can cause additional hydrate dissolution, resulting in further pressure increases. The modeling of this dissociation has been done by Wright et al. (2005) and by Davies et al. (2006). [Pg.677]

Particle Size of Raw Materials in Solution Particle size is affected by the breaking process of the particle, crystal form, and/or salt form of the drug. The particle size can affect the rate of dissolution of raw materials in the manufacturing process. Raw materials of a finer particle size may dissolve faster because they have a larger surface area in contact with the solvent than those of a larger particle size when the product is compounded [6], Mixing faster causes the particle to break down and dissolve more quickly. In addition, hydrated particles are less soluble than their anhydrous partners [37],... [Pg.327]

Another consequence of the presence of water in natural gas and acid gas is the formation of solid compounds called hydrates. Hydrates are important because they form at conditions where a solid phase would not otherwise be expected. In addition, hydrates are notorious for plugging production and processing facilities. In this chapter, we will examine hydrates as they relate to acid gas injection. [Pg.131]

Fig. 8. (A) Measured forces between two charged mica surfaces in 10" M KCl, where beyond 30 A (and out to 500 A) the repulsion is well described by conventional electrostatic double-layer force theory. Below 30 A there is an additional hydration repulsion, with oscillations superimposed below 15 A. (B) Forces between two uncharged lecithin bilayers in the fluid state in water. At long range there is an attractive van der Waals force, and at short range (i.e., below 25 A) there is a monotonically repulsive steric hydration force. (C) Forces between two hydrophobized mica surfaces in water where the hydrophobic interaction is much stronger than could be expected from van der Waals forces alone. From Israelachvili and Marra (1986). Fig. 8. (A) Measured forces between two charged mica surfaces in 10" M KCl, where beyond 30 A (and out to 500 A) the repulsion is well described by conventional electrostatic double-layer force theory. Below 30 A there is an additional hydration repulsion, with oscillations superimposed below 15 A. (B) Forces between two uncharged lecithin bilayers in the fluid state in water. At long range there is an attractive van der Waals force, and at short range (i.e., below 25 A) there is a monotonically repulsive steric hydration force. (C) Forces between two hydrophobized mica surfaces in water where the hydrophobic interaction is much stronger than could be expected from van der Waals forces alone. From Israelachvili and Marra (1986).
Wet extmders are also used ahead of a number of soybean solvent extraction plants. In plants with undersized extractors, the energy used by the extruder can be compensated by additional oil yield from the extractor. Steam consumption is reduced in the desolventizer toaster. Additionally, the wet extruder in a soybean plant increases temperature sufficiently to stop the phospholipase enzyme from converting additional hydratable phosphatides into nonhydratable phosphatides. This reduces acid, caustic, and silica consumption in the downstream refinery. However, in soybean plants with adequately sized extractors where potential oil yield... [Pg.2481]

The glycolytic pathway includes three such reactions glucose 6-phosphate isomer-ase (1,2-proton transfer), triose phosphate isomerase (1,2-proton transfer), and eno-lase (yS-elimination/dehydration). The tricarboxylic acid cycle includes four citrate synthase (Claisen condensation), aconitase (j5-elimination/dehydration followed by yS-addition/hydration), succinate dehydrogenase (hydride transfer initiated by a-proton abstraction), and fumarase (j5-elimination/dehydration). Many more reactions are found in diverse catabolic and anabolic pathways. Some enzyme-catalyzed proton abstraction reactions are facilitated by organic cofactors, e.g., pyridoxal phosphate-dependent enzymes such as amino acid racemases and transaminases and flavin cofactor-dependent enzymes such as acyl-C-A dehydrogenases others. [Pg.1107]

Nucleophilic addition Hydrated La(OTf)3 is a useful Lewis acid catalyst for the addition of nucleophiles to Al-phosphinyhmines. In the presence of (Cp3C0)20 the A-substitutent is also changed into a trifluoroacetyl group. [Pg.272]

Proteins adsorbed at an oil-water interface may stabilize the oil droplets by the Derjaguin, Landau, Verwey, and Overbeek (DLVO) interactions and/or the steric stabilization mechanism. The proteins may possess or be capable of adopting extended structures, which protrude into a solution for a considerable distance from the interface. This extended hydrated layer may form the basis for steric stabilization of the emulsion. Interactions between the adsorbed protein layers can involve a reduction in conhgurational entropy as molecular chains overlap (Darling and Birkett, 1987). In addition, hydration of adsorbed hydrophilic components can lead to an enthalpic repulsion when two particles are in close proximity. This tends to force the oil droplets apart (Darling and Birkett, 1987). [Pg.261]

The previously described measurements have been performed on lipids in aqueous solutions, but lipid bilayers also swell in some other solvents (12) and the results of such measurements compare quite well with the aqueous case. In addition, hydration (solvation) forces act between DNA polyelectrolytes (13) and polysaccharides (14). These facts make the interpretation of the forces even more complicated and it is no wonder that different approaches to explain the nature of this solvation force exist. So far no truly ab initio theory has been proposed. The existing theories include models based on the electrostatic approach, the free energy approach, and an approach based on the entropic or protrusion model. [Pg.16]

Additional hydration of hydrolysis products - Release of Pi allows greater opportunities for hydration. Hydration is an energetically favored state. [Pg.1825]

Additional Hydration of the Hydrolysis Products Electrostatic Reulsion Between Charged Products... [Pg.2335]

In each case, the reaction proceeds with syn-addition (hydration) and anti-Markovnikov orientation. [Pg.573]

Some of the above processes efficiently remove heavy metals, while others minimise the re-formation of dioxins and furans. In addition, hydrated Ume may be used in conjunction with activated carbon or lignite coke for removal of dioxins, furans and volatile heavy metals. [Pg.333]


See other pages where Addition Hydration is mentioned: [Pg.244]    [Pg.75]    [Pg.29]    [Pg.353]    [Pg.433]    [Pg.217]    [Pg.176]    [Pg.584]    [Pg.77]    [Pg.98]    [Pg.222]    [Pg.442]    [Pg.185]    [Pg.108]    [Pg.275]    [Pg.99]    [Pg.573]    [Pg.94]    [Pg.481]    [Pg.1649]   


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