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Convenience

A rigorous relation exists between the fugacity of a component in a vapor phase and the volumetric properties of that phase these properties are conveniently expressed in the form of an equation of state. There are two common types of equations of state one of these expresses the volume as a function of... [Pg.15]

It is strictly for convenience that certain conventions have been adopted in the choice of a standard-state fugacity. These conventions, in turn, result from two important considerations (a) the necessity for an unambiguous thermodynamic treatment of noncondensable components in liquid solutions, and (b) the relation between activity coefficients given by the Gibbs-Duhem equation. The first of these considerations leads to a normalization for activity coefficients for nonoondensable components which is different from that used for condensable components, and the second leads to the definition and use of adjusted or pressure-independent activity coefficients. These considerations and their consequences are discussed in the following paragraphs. [Pg.17]

However, if the liquid solution contains a noncondensable component, the normalization shown in Equation (13) cannot be applied to that component since a pure, supercritical liquid is a physical impossibility. Sometimes it is convenient to introduce the concept of a pure, hypothetical supercritical liquid and to evaluate its properties by extrapolation provided that the component in question is not excessively above its critical temperature, this concept is useful, as discussed later. We refer to those hypothetical liquids as condensable components whenever they follow the convention of Equation (13). However, for a highly supercritical component (e.g., H2 or N2 at room temperature) the concept of a hypothetical liquid is of little use since the extrapolation of pure-liquid properties in this case is so excessive as to lose physical significance. [Pg.18]

For a noncondensable component, therefore, it is convenient to use a normalization different from that given by Equation (13) in its place we use... [Pg.18]

The pressure at which standard-state fugacities are most conveniently evaluated is suggested by considerations based on the Gibbs-Duhem equation which says that at constant temperature and pressure... [Pg.20]

We can now consider the most convenient form for writing the liquid-phase fugacity of component i. First we consider a condensable component and write... [Pg.21]

Because of the approximation given by Equation (22), we obtain a convenient method for determining f for a noncondensable... [Pg.23]

For liquid mixtures containing both condensable and noncondensable components. Equation (15) is applicable. However it is now convenient to rewrite that equation. Neglecting, as before, the last term in Equation (15), we obtain ... [Pg.88]

The preference is for a process based on ethylene rather than the more expensive acetylene and chlorine rather than the more expensive hydrogen chloride. Electrolytic cells are a much more convenient and cheaper source of chlorine than hydrogen chloride. In addition, we prefer to produce no byproducts. [Pg.17]

The composite curves are useful in providing conceptual understanding of the process, but the problem table algorithm is a more convenient calculation tool. [Pg.179]

Before suggesting an approach for predicting the minimum number of shells for an entire network, a more convenient method for determining the number of shells in a single unit must first be found. Adopting the design criterion given by Eq. (7.13) as the basis, then any need for trial and error can be eliminated, since an explicit... [Pg.225]

Decomposition of its internal salt (a zwitter-ion) provides a convenient source of benzyne for organic synthesis. [Pg.36]

Soluble in water and alcohol. It is a very feeble base. It occurs in beets and mangolds and many other plants, and can conveniently be prepared from beet molasses. [Pg.59]

CCls CHO. A colourless oily liquid with a pungent odour b.p. 98°C. Manut actured by the action of chlorine on ethanol it is also made by the chlorination of ethanal. When allowed to stand, it changes slowly to a white solid. Addition compounds are formed with water see chloral hydrate), ammonia, sodium hydrogen sulphite, alcohols, and some amines and amides. Oxidized by nitric acid to tri-chloroethanoic acid. Decomposed by alkalis to chloroform and a methanoate a convenient method of obtaining pure CHCI3. It is used for the manufacture of DDT. It is also used as a hypnotic. [Pg.91]

When the fats are heated above 250"C they decompose with the production of acrolein, the intense smell of which is one of the best methods for detecting fats. The extraction of fats from tissues is most conveniently carried out by extraction with ether or some other solvent. [Pg.172]

A mixture of polymethylene glycols of the type (CH20) ,xH20 where n is 6- 50. It is a white, amorphous powder having the odour of meth-anal, m.p. I20-130°C. The commercial product contains 95% methanal and is obtained in while flocculent masses when solutions of methanal are evaporated or allowed to stand. When heated it is converted to methanal. Used as a convenient solid substitute for methanal. [Pg.296]

Occurs in the high-boiling fraction of coal tar. Most conveniently prepared by Skraup s reaction by healing a mixture of aniline, glycerol, sulphuric acid and nitrobenzene. Used in the manufacture of dyestuffs, and pharmaceutical products. [Pg.338]

The maximum concentration atltainable under such conditions is termed the solubility of the substance at the specific temperature used in the experiment, since solubility generally increases with rising temperature. Solubility is usually expressed in grams per 100 g of solvent, or grams per 100 g of solution. Sometimes, for practical convenience, it may be expressed in grams per 100 ml of solvent or solution. [Pg.367]

The sulphonic acids are usually prepared by the action of sulphuric acid upon a compound. The concentration of the acid and the temperature of reaction are varied according to the reactivity of the compound. Often oleum is used or even chiorosulphonic acid. Alternatively sulphur trioxide complexed to pyridine or dioxan can be used with reactive substrates. Aminosulphonic acids such as sulphanilic and naphthionic acids are most conveniently prepared by heating the sulphate of the amine at ISO C. [Pg.378]

If triphenylmethyl chloride in ether is treated with sodium, a yellow colour is produced due to the presence of the anionic spiecies PhsC". Alternatively, if triphenylmethyl chloride is treated with silver perchlorate in a solvent such as THF, the triphenylmethyl cation is obtained. More conveniently, triphenylmethyl salts, PhsC X", can be obtained as orange-red crystalline solids from the action of the appropriate strong acid on triphenylcarbinol in ethanoic or propanoic anhydride solution. The perchlorate, fluoroborate and hexafluoro-phosphate salts are most commonly used for hydride ion abstraction from organic compounds (e.g. cycloheptatriene gives tropylium salts). The salts are rather easily hydrolysed to triphenylcarbinol. [Pg.406]

The above equation is valid at low pressures where the assumptions hold. However, at typical reservoir temperatures and pressures, the assumptions are no longer valid, and the behaviour of hydrocarbon reservoir gases deviate from the ideal gas law. In practice, it is convenient to represent the behaviour of these real gases by introducing a correction factor known as the gas deviation factor, (also called the dimensionless compressibility factor, or z-factor) into the ideal gas law ... [Pg.106]


See other pages where Convenience is mentioned: [Pg.14]    [Pg.15]    [Pg.17]    [Pg.40]    [Pg.41]    [Pg.56]    [Pg.82]    [Pg.113]    [Pg.340]    [Pg.159]    [Pg.189]    [Pg.211]    [Pg.401]    [Pg.108]    [Pg.119]    [Pg.123]    [Pg.131]    [Pg.132]    [Pg.133]    [Pg.163]    [Pg.166]    [Pg.203]    [Pg.226]    [Pg.251]    [Pg.289]    [Pg.313]    [Pg.368]    [Pg.374]    [Pg.375]    [Pg.388]   
See also in sourсe #XX -- [ Pg.185 ]

See also in sourсe #XX -- [ Pg.92 ]




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