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Liquid Aqueous Phase

Because electrochemical corrosion reactions proceed only in a liquid aqueous phase, the chemical composition and properties determined by chemical composition of this phase are most important to consider. This phase is largely water and will be called water in the subsequent discussion. Water enters the various refinery process units in a number of ways. Of prime importance is water that is entrained and/or emulsified in the crude oil charge to the refinery, i.e. the feed to the crude still. This water is produced with crude oil and remains with the crude, despite oil-field separators, liquid traps in pipelines, etc. Although the amount of water is usually small in total volume, its effect on corrosion may be large, since it usually contains a high proportion of corrosive dissolved salts, mainly chlorides of sodium, calcium, and magnesium. [Pg.206]


First, the simple thermodynamic description of pe (or Eh) and pH are both most directly applicable to the liquid aqueous phase. Redox reactions can and do occur in the gas phase, but the rates of such processes are described by chemical kinetics and not by equilibrium concepts of thermodynamics. For example, the acid-base reaction... [Pg.421]

CL is observed in the liquid, gas, and solid phases. In the last decade, there has been growing interest in CL as a detection technique for quantitative analysis, particularly in the liquid (aqueous) phase [2, 3], which will be solely dealt with in this chapter, because of the excellent sensitivity and wide dynamic ranges that can be achieved by using relatively simple and inexpensive instrumentation. [Pg.176]

Fig. 5 The three-step process of nanocasting . First, a condensed LLC phase is formed, with the inorganic precursors occupying the liquid (aqueous) phase. Second, the inorganic molecules are solidified by some chemical or electrochemical means. Third, the LLC template is removed, leaving a mesoporous structure. Partially reproduced with permission from [32], 2002 by the Royal Society of Chemistry... Fig. 5 The three-step process of nanocasting . First, a condensed LLC phase is formed, with the inorganic precursors occupying the liquid (aqueous) phase. Second, the inorganic molecules are solidified by some chemical or electrochemical means. Third, the LLC template is removed, leaving a mesoporous structure. Partially reproduced with permission from [32], 2002 by the Royal Society of Chemistry...
In the stroma region, a liquid aqueous phase containing water soluble globular enzymes, the carbon dioxide is reduced to carbohydrates. The reduction needs an ap-... [Pg.46]

Basso A, Spizzo P, Toniutti M et al. (2006) Kinetically controlled synthesis of ampidllin and cephalexin in highly condensed systems in the absence of a liquid aqueous phase. 1 Mol Catal B Enzym 39 105-111... [Pg.285]

Zeolite syntheses start from alkaline aqueous mixtures of aluminum and silicon compounds. The reactions are sometimes carried out at atmospheric pressure but more often in a high-pressure autoclave. The controlled crystallization of a particular zeolite requires careful control of the concentration and stoichiometry of the reaction partners, the temperature, and the shearing energy of the stirrer. After mixing of the liquid phase and formation of a gel, a transition of the gel phase in to the liquid aqueous phase occurs, whereby crystalline zeolites are formed from the amorphous particles. [Pg.242]

Radicals exist is the gas and liquid (aqueous) phase. They play an important role in many chemical transformations. In natural waters, radical ions, a radical that carries an electric charge, exist. Those positively charged are called radical cations and those negatively charged radical anions, but the most important is the superoxide anion OJ. Free radicals are produced under high temperature (combustion. [Pg.379]

D7. Aniline and water are partially miscible and form a heterogeneous azeotrope. At p = 778 mm Hg the azeotrope concentrations are The vapor is 0.0364 mole frac aniline, the liquid aqueous phase contains 0.0148 mole frac aniline, and the liquid organic phase contains 0.628 mole frac aniline. Estimate the relative volatility of water with respect to aniline in the organic phase. Note Be careful to use the mole fracs of the correct conponent. [Pg.335]

If volatile organic substances are present in a water sample, and the water is kept in a closed thermostated system, a balance of vapour pressure is established between the liquid aqueous phase and the gas phase. The estab-... [Pg.166]

The preparation of various studies with fluid systems at high or supercritical temperatures often involves the occurence of droplets and emulsions. This makes it desirable to know of the surface tension of the liquid aqueous phase in contact with gas... [Pg.318]

Figure 9.1 Cellulose transformation in the presence of MNP-NH -Ru and MNP-Ru catalysts. (Reaction conditions 0.06 g catalyst, 0.14 g cellulose, 5 mL water, 180°C, 2 h, 1200 rpm. Note Dtuing each catalyst test the autogenic presstue was 4 atm that also demonstrate that not aU water evaporated and the reaction took place in the liquid aqueous phase.)... Figure 9.1 Cellulose transformation in the presence of MNP-NH -Ru and MNP-Ru catalysts. (Reaction conditions 0.06 g catalyst, 0.14 g cellulose, 5 mL water, 180°C, 2 h, 1200 rpm. Note Dtuing each catalyst test the autogenic presstue was 4 atm that also demonstrate that not aU water evaporated and the reaction took place in the liquid aqueous phase.)...
As discussed in Section 22.2.3, residual hydrocarbons in the reformate can be found as a separated organic Hquid phase in the gas phase and in soluble form in the liquid aqueous phase. The maximum solubilities of species such as benzene and alkanes are given in Table 22.9. These values, however, are misleading as the real behavior differs from that of ideal hquids. For an infinite dilution of hydrocarbons in water and for an ideal mixing in the gas phase, Eq. (22.48) can be written as... [Pg.632]

The carbons obtained from wood have a large pore volume but a low hardness and density and are therefore generally used in liquid (aqueous) phase applications. These carbons are not very suitable for vapour adsorption applications. The carbons obtained from hard coal have a large pore volume and a high hardness and density, and are used in gas/vapour adsorption applications. Activated carbons obtained from soft coal have a medium pore volume, hardness and density and can therefore be used in both vapour phase and liquid phase applications. Lignite produces hard carbons with a small micropore volume and is generally preferred in aqueous applications. Coconut shells or other nut shells produce hard carbons with large micropore volumes suitable mainly for vapour phase applications. [Pg.70]

First of all, the particles reach the interphase between the fluid phases. This is realized due to the destabilizing conditions within the magnetite suspension (aqueous phase). This means that the magnetite nanoparticles have surface charges in the aqueous phase, which lead to the formation of an interfacial potential between the solid and liquid aqueous phases. Thus, the particle surface is polar or, rather, hydrophilic as a result of the attachment of water molecules or hydroxyl ions to the iron ions of magnetite. Depending on the pH value of the aqueous phase, the dissociation of the hydroxyl groups takes place [17], as shown in Fig. 3. [Pg.374]

Instantaneous corrosion rate meters all have the advantages of detecting very rapid changes in the rate of corrosion without disturbing the corrosion process. The measurements can be made at locations distant from the location of the electrodes. A disadvantage, as with all current-voltage methods, is that the measurements must be taken in a liquid, aqueous phase that has a reasonable electrical conductivity. [Pg.277]

Affinity partitioning between two liquid (aqueous) phases has been used to isolate the EcoRI enzyme free from contaminating nuclease activities (76). [Pg.265]


See other pages where Liquid Aqueous Phase is mentioned: [Pg.314]    [Pg.314]    [Pg.117]    [Pg.117]    [Pg.117]    [Pg.359]    [Pg.379]    [Pg.34]    [Pg.448]    [Pg.1263]    [Pg.413]    [Pg.209]    [Pg.98]    [Pg.701]    [Pg.146]    [Pg.594]    [Pg.395]    [Pg.265]    [Pg.107]    [Pg.206]    [Pg.74]    [Pg.515]    [Pg.433]   


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Aqueous liquids

Aqueous phase liquid extractor

Dense non-aqueous phase liquids

Dense non-aqueous phase liquids (DNAPLs

Light non-aqueous phase liquids

Liquid phase models, aqueous systems

Liquid-solid chromatography aqueous mobile phases

Non-aqueous phase liquid

Reversed-phase liquid chromatography aqueous samples

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