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Principal point

The principal point of interest to be discussed in this section is the manner in which the surface tension of a binary system varies with composition. The effects of other variables such as pressure and temperature are similar to those for pure substances, and the more elaborate treatment for two-component systems is not considered here. Also, the case of immiscible liquids is taken up in Section IV-2. [Pg.65]

Smits first established experimentally that phase behavior of the type shown in Fig. 8 is possible, with his classic investigation of the system ethyl ether + anthraquinone.76-83 83 84 The temperature and pressure of the principal points of the phase diagram are... [Pg.94]

Stability (Classical Theory).—In recent years the question of stability has acquired a considerable importance in applications.9 Here we shall discuss briefly the principal points in the two major trends in studies of stability. [Pg.343]

Pharmacologically, a principal point relates to the cost-effectiveness of the newer indications for SSRIs in the less common disorders such as obsessive—compulsive disorder and social phobia. These conditions do place a disproportionate burden on health-care systems, and clinical trials of the newer indications are convincing. However, no cost-effectiveness study has yet been petformed to assess this, and prescribing will continue to be based on individual clinical need. [Pg.96]

The Process in the Philosophical Work considered as thoroughly analogical with that in Man s Redemption through Jesus Christ and represented by positions given thereof, as to its principal points in Behmen s Signatura Rerum, chapters, vii, x, xi, xii. [Pg.120]

At this point we leave the conventional kinetic theory and turn to the substance of our Section 2.5.2. The principal point made there is that for polymerisations in bulk the propagation reaction is not bimolecular but unimolecular, so that the rate is given by Equation (39) ... [Pg.532]

However, reaction a in scheme 7.38 did not take place, irrespective of solvent polarity or the strength of the base. UV irradiation did not help either. Nevertheless, the cyclization appears to be successful in the presence of acetone (see reaction c in Scheme 7.38 Bowman et al. 1982). As usual, inhibitors stop this anion-radical reaction 3-iodothiobenzanilide does not experience the cyclization. A principal point of this reaction consists of the understandable formation of the bond between the carbon-radical center and the negatively charged sulfur. Such a reaction is typical. [Pg.374]

The double bond functions in a very analogous manner. It too interrupts effective chain length and determines the principal point of oxidative attack. In a manner quite analogous to the methyl group, through changes in the combustion velocity, the double bond also alters the octane number and critical compression ratio. [Pg.371]

The two principal points, in which the conclusions drawn by Dr, Fite from these results differ from Fkankiand s, are—first, his high estimate of the powers of the Boghead cancel distilled alone and, secondly, the comparatively low results which he obtained by the collateral use of water gas. The first of these points arises, us just mentioned, from reliance being placed upon certain results obtained in small retorts with seven pound charges of cannel, which results differ most widely from those of all other experiments, os also from the previously published report of Dr, Fyee himself. [Pg.155]

Continual rotation of the melted mass is the principal point to be attended to in most of the glass-blower s operations but these will bo best described in connection with the special manufacture of the different varieties of glass,... [Pg.208]

Converging lines of evidence have led to a general acceptance of the monomeric metaphosphate mechanism for the hydrolysis of phosphate monoester monoanions. The pH rate profile for aryl and alkyl phosphate monoester hydrolyses commonly exhibits a rate maximum near pH 4. where the concentration of the monoanion is at a maximum. The proposed mechanism is based on these principal points of evidence (a) a general observation of P-O bond cleavage (b) the entropies of activation for a series of monoester monoanions are all close to zero, which is consistent with a unimolecular rather than a bi-molecular solvolysis where entropies of activation are usually more negative by 20 eu7 (c) the molar product composition (methyl phosphate inorganic phosphate) arising from the solvolysis of the monoester monoanion in a mixed methanol-water solvent usually approximates the molar ratio of methanol ... [Pg.1]

The work of Panyutin (155), Levedahl (106), Boord (19), and Cramer and Campbell (35) suggested a high reactivity at the 2° C—H bonds. On the basis of his work Levedahl believed these bonds were the principal points of initial attack. Livingston (113) arrived at an order 2° 3° > 1° without directly associating this with the initial attack. Cullis (38) and Malherbe and Walsh (130) have reported evidence for attack at 2° C—H bonds. Malmberg and coworkers (132) decided, on the basis of analysis of products, that 2°... [Pg.194]

Despite the fact that from a principal point of view a problem of concentration oscillations could be considered as solved [4], satisfactory theoretical descriptions of experimentally well-studied particular reactions are practically absent. Due to very complicated reaction mechanism (in order to describe the Belousov-Zhabotinsky reaction even in terms of standard chemical kinetics several tens of concentration equations for intermediate products should be written down and solved numerically [4, 9, 10]) these equations contain large number of ill-defined parameters - reaction rates [10]. [Pg.468]

In this section, group transfer reactions in which the product molecule A-B is vibrationally excited but still in its ground electronic state are considered. (Transfer reactions that produce electronic excitation are discussed in Section 3.4.) The available experimental evidence is tabulated. Only typical examples are described. The principal points discussed are the limitations that experimental technique has imposed on observation and interpretation of this type of chemi-excitation and the extraction of generalizations concerning this class of reaction. [Pg.118]

Abstract This article summarizes the principal points of discussions at the Erice... [Pg.79]

The principal points of current interest concerning Wolffram s-red type complexes and on which research is being concentrated are... [Pg.59]

Fig. 4. Primary structure and sites of phosphorylation of 0-CN A2-5P, showing the principal points of cleavage by plasmin (V) (Eigel et al., 1984 Stewart et al., 1987). Fig. 4. Primary structure and sites of phosphorylation of 0-CN A2-5P, showing the principal points of cleavage by plasmin (V) (Eigel et al., 1984 Stewart et al., 1987).
Figure 9 illustrates an example in which the object has a uniform diffusion surface of area S, reflectance R, the focal length of the lens /, the distance from the surface of the object to the principal point on the front of the lens is a, and the distance from the principal point on the reverse of the lens to the sensor plane is b—giving the well-known formula ... [Pg.15]

The factors which cause an increase in melt viscosity of molten, unplasticized PVC are also responsible for the gelation of solutions of homo- and/or copolymer (I). For that matter, an analogous explanation is envoked, and it has been shown that displacement of simple ligands on the metal soaps by chelating types of ligands—i.e., those which possess pi-electron rich substituents adjacent to the principal point of attachment, will reverse gelation. [Pg.59]

Certainly, the cluster calculations require some modification of quantum-chemical computational schemes. This is primarily connected with the main drawback of the cluster approximation, consisting of artificial scission of the chemical bonds between the cluster and the rest of the lattice. In most cases, however, such modifications do not involve the principal points, and therefore widely used quantum-chemical computer programs can serve as the basis for the cluster calculations. Some quantum-chemical methods used in... [Pg.134]


See other pages where Principal point is mentioned: [Pg.370]    [Pg.48]    [Pg.361]    [Pg.359]    [Pg.53]    [Pg.207]    [Pg.103]    [Pg.420]    [Pg.120]    [Pg.203]    [Pg.112]    [Pg.219]    [Pg.116]    [Pg.58]    [Pg.150]    [Pg.66]    [Pg.539]    [Pg.956]    [Pg.371]    [Pg.473]    [Pg.554]    [Pg.130]    [Pg.364]    [Pg.474]    [Pg.12]    [Pg.82]    [Pg.115]    [Pg.34]    [Pg.36]    [Pg.95]    [Pg.5]   
See also in sourсe #XX -- [ Pg.5 , Pg.10 ]




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Principal Nomenclatural Points

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