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The two basic equations

So far two basic equations of the theory have been deduced one involving and pj, and the [Pg.367]

But note both the Poisson and the MaxweU-Boltzmann equations have in them, with the other quantities being pj and , and so the problem now reduces to  [Pg.368]

Finding a relation between the smeared out pj of Poisson s equation and the n, corresponding to the discrete ions of the Maxwell-Boltzmann distribution. [Pg.368]

7 Step 5 The problem is to combine the Poisson equation with the Maxwell-Boltzmann equation - how can this be done  [Pg.368]

The problem is to get some device which would substitute the average distribution of the discrete ions in the ionic atmosphere around the centralj-ion, given by n, in the Maxwell-Boltzmann expression, by a continuous charge density which could be taken to be equivalent to pj in the Poisson equation. This would enable Poisson s equation to be combined with a Maxwell-Boltzmann distribution. [Pg.368]


By multiplying [A] x [B] we can calculate the two basic equation systems to use in solving this problem as ... [Pg.20]

Division of the two basic equations given above results in ... [Pg.308]

To see why this is so, we must consider the two basic equations involved, namely,... [Pg.343]

Having demonstrated that exact solution for the mean concentrations (c, (x, t j) even of inert species in a turbulent fluid is not possible in general by either the Eulerian or Lagrangian approaches, we now consider what assumptions and approximations can be invoked to obtain practical descriptions of atmospheric diffusion. In Section 18.4 we shall proceed from the two basic equations for (c,), (18.4) and (18.8), to obtain the equations commonly used for atmospheric diffusion. A particularly important aspect is the delineation of the assumptions and limitations inherent in each description. [Pg.833]

In analysis of osmotic flow and net solute movement, the two basic equations... [Pg.34]

The two basic laws of kinetics are the law of mass action for the rate of a reac tion and the Arrhenius equation for its dependence on temperature. Both of these are strictly empirical. They depend on the structures of the molecules, but at present the constants of the equations cannot be derived from the structures of reac ting molecules. For a reaction, aA + hE Products, the combined law is... [Pg.2071]

The two basic principles permit the algebraic manipulation of chemical reactions (represented by their stoichiometric equations and associated enthalpy changes) in order to achieve desired thermochemical results. [Pg.353]

The models developed for the low salt concentrations (0.0 and 0.1 M NaCl) were very different from those for the high salt concentration. The two basic Independent variables used were salt level and the absolute value of the pH minus 4.0. To avoid Implying that the behavior of each functional property on either side of pH 4.0 Is the mirror Image of Its behavior on the other side of pH 4.0, two variables were formed from the absolute value of pH minus 4.0. These were the absolute values of pH minus 4.0 for each pH above 4.0 (values of this variable for observations In which the pH was less than 4.0 were set equal to zero) and the absolute values of pH minus 4.0 for each pH below 4.0 (values of this variable for observations In which pH was greater than 4.0 were set equal to zero). As shown In the table, these basic variables were used In the estimated models along with their squares, their Interactions with salt level (0.0 and 0.1 M NaCl), and salt level to form the Independent variables In the final equations used. Other variables, such as cubic powers of pH minus 4.0, were tried and discarded due to lack of statistical significance In arriving at the final models. [Pg.309]

The formulae of 5.2 seem to be less algebraically tractable for the equations appropriate to flow reactors than for those from closed systems. (This is basically because we can eliminate all the terms involving one of the variables by adding the two rate equations together. For flow systems this cancellation does not occur because of the outflow terms.) Nevertheless, the various coefficients can be evaluated implicitly without much problem and the stability parameter p2 calculated. The following situation is found for the particular case of interest here, fi0 = 0. [Pg.225]

Here we develop the basic logic and the algebraic steps in a modern derivation of the Michaelis-Menten equation, which includes the steady-state assumption introduced by Briggs and Haldane. The derivation starts with the two basic steps of the formation and breakdown of ES (Eqns 6-7 and 6-8). Early in the reaction, the concentration of the product, [P], is negligible, and we make the simplifying assumption that the reverse reaction, P—>S (described by k 2), can be ignored. This assumption is not critical but it simplifies our task. The overall reaction then reduces to... [Pg.204]

When a second nitrogen atom is introduced into the pyridine ring the basicity is reduced (pjRTa 5.23 for pyridine and 2.33 for pyridazine). The effect of the additional substituents on pKK depends on the position of the substituents (Table 3). An extensive set of pK values of pyridazine derivatives has been submitted to correlation analysis using the Hammett and the two Taft equations, which shows that the pKa values are most sensitive to the effect of a 2-substituent followed by the effects of 3- and 4-substituents. The interactions between nitrogen atom and 2-substituents represent over 70% of the inductive character. The composition of the effects of +M 4-substituents is significantly enriched in the resonance interactions, whereas -M 4-substituents interact with the nitrogen atom mainly by induction (77MI21201). [Pg.1223]

Combining the first two basic equations of a steadily propagating regime, specifically the equations of conservation of mass and momentum, so as to obtain the equation... [Pg.422]

For the solution of a salt composed of two ionizable species (binary electrolyte), the four basic equations can be combined to yield the convective diffusion equation for steady-state systems ... [Pg.243]

The transport of solutes through a membrane can be described by using the principles of irreversible thermodynamics (IT) to correlate the fluxes with the forces through phenomenological coefficients. For a two-components system, consisting of water and a solute, the IT approach leads to two basic equations [83],... [Pg.61]

PARAFAC refers both to the parallel factorization of the data set R by Equation 12.1a and Equation 12.lb and to an alternating least-squares algorithm for determining X, Y, and Z in the two equations. The ALS algorithm is known as PARAFAC, emanating from the work by Kroonenberg [31], and as CANDECOMP, for canonical decomposition, based on the work of Harshman [32], In either case, the two basic algorithms are practically identical. [Pg.491]

The theory of relativity and quantum mechanics constitute the two basic foundations of theoretical physics. It is also well known that quantum mechanics based upon the Schrodinger equation has been used for decades to investigate atomic and molecular structure by physicists and chemists. However, the Schrddinger equation is non-relativistic i.e., it is not Lorentz-invariant as it does not obey the special theory of relativity. [Pg.291]

Basic Equations. The relationship between microbial growth and substrate utilization can be formulated in two basic equations (2, 7). Equation 1 describes the relationship between net rate of growth of microorganisms and the rate of utilization of the growth limiting substrate ... [Pg.164]

When a protein is measured by UV and RI detectors, the following two basic equations can be used to express the relation of the parameters ... [Pg.114]

According to the Swain-Lupton approach (SL), the a electronic constant is defined as a linear combination of the two basic electronic contributions [Swain and Lupton Jr., 1968 Swain et al., 1983 Swain, 1984 Reynolds and Topsom, 1984] based on the equation ... [Pg.151]

In order to take into account carefully the analytical data concerning the electrochemical reaction to be carried out, two basic equations must be recalled ... [Pg.321]

The theoretical derivation of extrathermodynamical relationships is based on the arbitrary division of a molecule into regions, usually two the basic structure R, and the substituent X (1, 2). An additivity postulate then enables one to express the partial free energy of the substance (or other related property) as a sum of independent contributions, each representing the arbitrarily defined parts, and an interaction term between the two parts (equation 1). [Pg.27]

The two basic flowsheet software architectures are sequential modular and equation-based. In sequential modular, we write each unit model so that it calculates output(s), given feed(s), and unit parameters. This is the most commonly used flowsheeting architecture at present, and examples include Aspen+ plus Hysys (AspenTech), ChemCAD, and PROll (SimSci). In equation-based (or open-system) architectures, all equations are written describing material and energy balances as algebraic equations in the form/(x) = 0. This is the preferred architecture for new simulators and optimization, and examples include Speedup (AspenTech) and gPROMS (PSE pic). Each is discussed in turn. [Pg.1338]


See other pages where The two basic equations is mentioned: [Pg.367]    [Pg.367]    [Pg.4]    [Pg.477]    [Pg.214]    [Pg.56]    [Pg.111]    [Pg.1320]    [Pg.451]    [Pg.155]    [Pg.397]    [Pg.1]    [Pg.53]    [Pg.1009]    [Pg.1181]    [Pg.135]    [Pg.246]    [Pg.1341]    [Pg.155]    [Pg.112]   


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