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Moser equation

Determine the rate taw parameters k, and X, assuming the data can be hi by the Moser Equation... [Pg.301]

There are several other empirical expressions, as the Moser equation ... [Pg.145]

No experiments appear to have been made with such cells, although the equation has been verified with oxygen at different partial pressures in admixture with nitrogen, with platinum electrodes and hot solid glass as electrolyte (Haber and Moser). A similar case is that of two amalgams of a metal, of different concentrations, as electrodes, and a solution of a salt of the metal as electrolyte (G. Meyer, 1891). Here we must take the osmotic pressures of the metals in the amalgams, Pi, P2, and, for an 7i-valent metal ... [Pg.464]

Equation 3.1 and Equation 3.2) (including the mean particle sizes obtained) (Adapted from Bonnemann, H. and Brijoux, W., in Surfactant-Stabilized Nanosized Colloidal Metals and Alloys as Catalyst Precursors/Advanced Catalysts and Nanostructured Materials, Moser, W., Ed., Academic Press, San Diego, 1996, pp. 165-196, Chap. 7. With permission from Elsevier Science.)... [Pg.69]

These partial quantities may either be used directly or transformed by means of the Gibbs-Duhem equation in the overall assessment of the system in question (Moser 1979). [Pg.87]

Certainly, Monod s formula has been used extensively in phenomenological (unstructured) models, although the literature presents other equations for one limiting substrate systems (Equations 17 and 18). In Moser s formulation it was necessary to introduce a third parameter ( n in Equation 17) to represent experimental data. [Pg.194]

Equations 1,2 and 5 can be combined into an extremely useful empirical expression that estimates room temperature electron tunneling rates for all proteins to within about an order of magnitude (Moser and Dutton, 1992) ... [Pg.8]

The Moser and Tessier growth laws are often used because (hey have been found to better fit experimental data at the beginning or end of fermentation. Other growth equations can be found in Dean. ... [Pg.215]

The rearrangements of phenols which are accompanied by hydroxy group transpositions are called the Wessely-Moser reaction (equations 50 and 51). In essence, these rearrangements are recyclizations of flavonoides 114 via the ring-opened form 115 to give the novel structures 116. Compounds that can participate in these rearrangements are flavones (114, R = H, R = Aryl), flavonoles (114, R = OH, R = Aryl), isoflavones (114, R = Aryl, R = H), chromones (114, R = H, R = Alkyl), chromonoles (114, R = OH, R = Alkyl), xanthones (114, R R = benzo) as well as benzopyrylium salts (e.g. see Reference 95). [Pg.748]

The conservation of mass equation for this situation, which is directly applied in modeling tube reactors (F. Moser, 1977) and bubble columns (Reuss, 1976), is thus identical to Equ. 3.3a. These types of one-dimensional one-phase models are not only necessary for calculating conversion They are also very useful in, for example, calculating the /cl value of a reactor with a concentration profile ... [Pg.122]

In App. II a computer simulation of this model equation in batch processes (A. Moser and Steiner, 1975) with varying values for is presented. The influence of a neglected value on the evaluation of Monod parameters in linearization diagrams is shown in Fig. 5.25, whereby false or even negative values for Kg can be the consequence (Grady et al., 1972). With the known value of ki, it is apparent that the undisturbed values for and Kg can be estimated (Moser and Steiner, 1975) only from a plot corresponding to Equ. 5.78... [Pg.227]

The appearance of this zero-order rate (BOD with respect to S) is seen in Fig. 5.39 (A. Moser, 1974). Several authors have developed a formal kinetic approach to biosorption effects (Busby and Andrews, 1975 A. Moser, 1977 Theophilou et al., 1978). Figure 5.40 illustrates the reaction scheme thought to be adequate as a starting point for the following set of model equations ... [Pg.239]

Figure 6.25. Demonstration of the advantage of CPFR over CSTR by calculating the volume ratio in dependence of conversion reached (C) as a function of biokinetics using the simple Monod equation and varying the ratio Sq/K and also product inhibition kinetics with variation of Sq/Kj. A. Moser, 1985c, reprinted with permission from Conservation and Recycling, vol. 8, No. 1/2, Pergamon Press, Oxford.)... Figure 6.25. Demonstration of the advantage of CPFR over CSTR by calculating the volume ratio in dependence of conversion reached (C) as a function of biokinetics using the simple Monod equation and varying the ratio Sq/K and also product inhibition kinetics with variation of Sq/Kj. A. Moser, 1985c, reprinted with permission from Conservation and Recycling, vol. 8, No. 1/2, Pergamon Press, Oxford.)...
Adler, M., and Moser J. On a class of polynomials connected with the Korteweg-de Vries equation. Comm, Math, Phys, (1978), 1-30. [Pg.326]

Airault, H., McKean, H. P., and Moser, J. Rational and elliptic solution of the Korteweg-de Vries equation and related many-body problem. Comm, Pure Appl, Math 30 (1977), 95-148. [Pg.326]

Expressions other that Equation 7.13 have also been suggested to describe cell growth rate, such as Contois (7.17), Moser (7.18), and Tessier (7.19) equations ... [Pg.161]

The starting materials for these complexes are dicarbonyl(cyclopentadienyl)-iron chloride (Fischer and Moser, 1970) and the dicarbonylcyclopentadienyl-iron anion [as the sodium salt (Green and Nagy. 1963)], both obtainable from tetracarbonyl (di-Tr-cyclopentadienyl)diiron which is available commercially. The reaction is carried out in tetrahydrofuran (THF). Equation (1) demonstrates the ease of manipulation of these substances in the preparation of an olefin complex from an epoxide. The tetrafluoroborate salt precipitates from ether. This reaction is also useful as a means of reducing expoxides stereospecifically to olefins with retention of configuration. The olefin is readily liberated from the complex by treatment with sodium iodide in acetone at room temperature for 15 min (Giering et ai, 1972). [Pg.4]

Capacity factors from HPLC are regarded as precise substitutes for log P values obtained by shake flask methods (Eadsforth and Moser 1983), if used within a congeneric series of compounds. Relating the BCFs to the lipophilic properties of the phenols resulted in equation (2) ... [Pg.50]


See other pages where Moser equation is mentioned: [Pg.273]    [Pg.215]    [Pg.397]    [Pg.425]    [Pg.380]    [Pg.273]    [Pg.215]    [Pg.397]    [Pg.425]    [Pg.380]    [Pg.672]    [Pg.7]    [Pg.1039]    [Pg.207]    [Pg.327]    [Pg.141]    [Pg.497]    [Pg.244]    [Pg.263]    [Pg.46]    [Pg.676]    [Pg.260]    [Pg.41]    [Pg.81]    [Pg.192]    [Pg.237]    [Pg.254]    [Pg.704]    [Pg.300]    [Pg.57]    [Pg.364]    [Pg.163]   
See also in sourсe #XX -- [ Pg.425 ]

See also in sourсe #XX -- [ Pg.217 ]




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