Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

A Derivation of Equation

A derivation of equation 49 is given in Reference 36. In flows of interest in MHD power generation the total pressure is about 101 kPa (1 atm) and the partial pressure of seed is 1 kPa (0.01 atm). Also, it is usually possible to assume that and that only one species (seed atoms) ionize. In rare... [Pg.419]

Appendix A Derivation of Equations for Polymer Concentration This Appendix shows the derivation of Equations (1) and (3) in the text. [Pg.519]

In the next section, we see how to deal quantitatively with solvation. Until now, the friction factor has been merely a proportionality factor of rather ill-defined origin. We shall not undertake a derivation of Equation (2) in any general sense. In the next section, however, we outline the derivation of an important result due to G. G. Stokes —the friction factor for an unsolvated sphere. [Pg.67]

If the main factors controlling tissue distribution are differences between plasma and tissue binding then a derivative of Equation (7.5) can be written. [Pg.126]

Green, A.E., Naghdi, P.M. (1976). A derivation of equations for wave propagation in water of variable depth. Journal of Fluid Mechanics 78 237-246. [Pg.640]

Kissinger [81] deduced the following equation by taking a derivative of Equation (6). [Pg.126]

Give a derivation of Equation 4.16d for the enhancement factor, using the procedure used to derive the catalyst effechveness factor. [Pg.156]

A. Derivation of Equations From the sketch in Fig. 12.1 of the slowing down scheme of fast neutrons in the reactor core, the relationship of p to the nonfission cadmium ratio will be derived for a more... [Pg.242]

Considerable experimental and theoretical material dealing with the spreading of droplets over a solid, nondeformable, dry surface has been accumulated for decades [10-13]. In the following text we present a derivation of equations that describe the kinetics of spreading in different situations. [Pg.174]

A differential equation for the time evolution of the density operator may be derived by taking the time derivative of equation (Al.6.49) and using the TDSE to replace the time derivative of the wavefiinction with the Hamiltonian operating on the wavefiinction. The result is called the Liouville equation, that is. [Pg.230]

Using a procedure similar to the derivation of Equation (4.13) the working equations of the U-V-P scheme for steady-state Stokes flow in a polar (r, 6) coordinate system are obtained on the basis of Equations (4.5) and (4.6) as... [Pg.116]

The equilibrium problem for a plate is formulated as some variational inequality. In this case equations (3.92)-(3.94) hold, generally speaking, only in the distribution sense. Alongside (3.95), other boundary conditions hold on the boundary F the form of these conditions is clarified in Section 3.3.3. To derive them, we require the existence of a smooth solution to the variational inequality in question. On the other hand, if we assume that a solution to (3.92)-(3.94) is sufficiently smooth, then the variational inequality is a consequence of equations (3.92)-(3.94) and the initial and boundary conditions. All these questions are discussed in Section 3.3.3. In Section 3.3.2 we prove an existence theorem for a solution to the variational equation and in Section 3.3.4 we establish some enhanced regularity properties for the solution near F. ... [Pg.200]

In the derivation of equations 24—26 (60) it is assumed that the cylinder is made of a material which is isotropic and initially stress-free, the temperature does not vary along the length of the cylinder, and that the effect of temperature on the coefficient of thermal expansion and Young s modulus maybe neglected. Furthermore, it is assumed that the temperatures everywhere in the cylinder are low enough for there to be no relaxation of the stresses as a result of creep. [Pg.85]

In a similar manner to the design process for packed columns, the physical characteristics and the performance specifications can be calculated theoretically for open tubular columns. The same protocol will be observed and again, the procedure involves the use of a number of equations that have been previously derived and/or discussed. However, it will be seen that as a result of the geometric simplicity of the open tubular column, there are no packing factors and no multi-path term and so the equations that result are far less complex and easier to manipulate and to understand. [Pg.385]

Omoleye, J. A., Adesina, A. A., and Udegbunam, E. O., Optimal design of nonisothermal reactors Derivation of equations for the rate-temperature conversion profile and the optimum temperature progression for a general class of reversible reactions, Chem. Eng. Comm., Vol. 79, pp. 95-107, 1989. [Pg.551]

Of course it should always be remembered that the solutions obtained in this way are only approximate since the assumptions regarding linearity of relationships in the derivation of equation (2.64) are inapplicable as the stress levels increase. Also in most cases recovery occurs more quickly than is predicted by assuming it is a reversal of creep. Nevertheless this approach does give a useful approximation to the strains resulting from complex stress systems and as stated earlier the results are sufficiently accurate for most practical purposes. [Pg.110]

Carbonylation ot 1-adamantyl triflate in the presence of tnflic acid also gives a derivative of homoadamantane as the result of a similar rearrangement with ring expansion [55] (equation 36)... [Pg.954]

The first two kinds of terms are called derivative integrals, they are the derivatives of integrals that are well known in molecular structure theory, and they are easy to evaluate. Terms of the third kind pose a problem, and we have to solve a set of equations called the coupled Hartree-Fock equations in order to find them. The coupled Hartree-Fock method is far from new one of the earliest papers is that of Gerratt and Mills. [Pg.240]

The importance of the Gibbs free energy and the chemical potential is very great in chemical thermodynamics. Any thermodynamic discussion of chemical equilibria involves the properties of these quantities. It is therefore worthwhile considering the derivation of equation 20.180 in some detail, since it forms a prime link between the thermodynamics of a reaction (AG and AG ) and its chemistry. [Pg.1231]


See other pages where A Derivation of Equation is mentioned: [Pg.414]    [Pg.434]    [Pg.84]    [Pg.315]    [Pg.183]    [Pg.377]    [Pg.241]    [Pg.414]    [Pg.434]    [Pg.84]    [Pg.315]    [Pg.183]    [Pg.377]    [Pg.241]    [Pg.618]    [Pg.1364]    [Pg.2253]    [Pg.43]    [Pg.73]    [Pg.504]    [Pg.90]    [Pg.178]    [Pg.92]    [Pg.118]    [Pg.48]    [Pg.102]    [Pg.450]    [Pg.1049]    [Pg.2016]    [Pg.322]    [Pg.122]    [Pg.357]    [Pg.294]    [Pg.461]    [Pg.168]   


SEARCH



Derivation of equations

Derivation of the Equations for Contact Shift and Relaxation in a Simple Case

Derivation of the Langevin equation from a microscopic model

Derivatives equations

Equation derivation

© 2024 chempedia.info