Balance equations differential form

CFD may be loosely thought of as computational methods applied to the study of quantities that flow. This would include both methods that solve differential equations and finite automata methods that simulate the motion of fluid particles. We shall include both of these in our discussions of the applications of CFD to packed-tube simulation in Sections III and IV. For our purposes in the present section, we consider CFD to imply the numerical solution of the Navier-Stokes momentum equations and the energy and species balances. The differential forms of these balances are solved over a large number of control volumes. These small control volumes when properly combined form the entire flow geometry. The size and number of control volumes (mesh density) are user determined and together with the chosen discretization will influence the accuracy of the solutions. After boundary conditions have been implemented, the flow and energy balances are solved numerically an iteration process decreases the error in the solution until a satisfactory result has been reached. 

The differential material balances contain a large number of physical parameters describing the structure of the porous medium, the physical properties of the gaseous mixture diffusing through it, the kinetics of the chemical reaction and the composition and pressure of the reactant mixture outside the pellet. In such circumstances it Is always valuable to assemble the physical parameters into a smaller number of Independent dimensionless groups, and this Is best done by writing the balance equations themselves in dimensionless form. The relevant equations are (11.20), (11.21), (11.22), (11.23), (11.16) and the expression (11.27) for the effectiveness factor. 

Isothermal Gas Flow in Pipes and Channels Isothermal compressible flow is often encountered in long transport lines, where there is sufficient heat transfer to maintain constant temperature. Velocities and Mach numbers are usually small, yet compressibihty effects are important when the total pressure drop is a large fraction of the absolute pressure. For an ideal gas with p = pM. JKT, integration of the differential form of the momentum or mechanical energy balance equations, assuming a constant fric tion factor/over a length L of a channel of constant cross section and hydraulic diameter D, yields,... 

Perform an overall material balance and the necessary component material balances so as to provide the maximum number of independent equations. In the event the balance is written in differential form, appropriate integration must be carried out over time, and the set of equations solved for the unknowns. 

In considering the flow in a pipe, the differential form of the general energy balance equation 2.54 are used, and the friction term 8F will be written in terms of the energy dissipated per unit mass of fluid for flow through a length d/ of pipe. In the first instance, isothermal flow of an ideal gas is considered and the flowrate is expressed as a function of upstream and downstream pressures. Non-isothermal and adiabatic flow are discussed later. 

The material balance was calculated for EtPy, ethyl lactates (EtLa) and CD by solving the set of differential equation derived form the reaction scheme Adam s method was used for the solution of the set of differential equations. The rate constants for the hydrogenation reactions are of pseudo first order. Their value depends on the intrinsic rate constant of the catalytic reaction, the hydrogen pressure, and the adsorption equilibrium constants of all components involved in the hydrogenation. It was assumed that the hydrogen pressure is constant during... 

The linearisation of the non-linear component and energy balance equations, based on the use of Taylor s expansion theorem, leads to two, simultaneous, first-order, linear differential equations with constant coefficients of the form... 

As shown in this chapter, in the simulation of systems described by partial differential equations, the differential terms involving variations with respect to length are replaeed by their finite-differenced equivalents. These finite-differenced forms of the model equations are shown to evolve as a natural eonsequence of the balance equations, according to the manner of Franks (1967). The approximation of the gradients involved may be improved, if necessary, by using higher order approximations. Forward and end sections can... 

The theory on the level of the electrode and on the electrochemical cell is sufficiently advanced [4-7]. In this connection, it is necessary to mention the works of J.Newman and R.White s group [8-12], In the majority of publications, the macroscopical approach is used. The authors take into account the transport process and material balance within the system in a proper way. The analysis of the flows in the porous matrix or in the cell takes generally into consideration the diffusion, migration and convection processes. While computing transport processes in the concentrated electrolytes the Stefan-Maxwell equations are used. To calculate electron transfer in a solid phase the Ohm s law in its differential form is used. The electrochemical transformations within the electrodes are described by the Batler-Volmer equation. The internal surface of the electrode, where electrochemical process runs, is frequently presented as a certain function of the porosity or as a certain state of the reagents transformation. To describe this function, various modeling or empirical equations are offered, and they... 

Effluent concentrations from a CSTR will be found for several kinds of Input by several methods, seven cases in all. The differential equations represent the material balances in the form Input = Output + Accumulation. 

The solids forwarding angle q> is related to rate by Eq. 5.7, and the force and torque balances provide the relationship between and the pressure gradient and q> using Eq. 5.23. Here, the equation is written in differential form so that integration can be performed numerically in the z direction using variable physical property data. 

Another key point of differentiation is the fact that nearly all PSA separations are bulk separations and any investigator interested in a high fidelity description of the problem of adsorption must solve a mass balance equation such as Eq. (9.9), the bulk separation equation, together with the uptake rate model and a set of thermal balance equations of similar form. In addition to the more complicated pde and its attendant boundary and initial conditions the investigator must also solve some approximate form of a momentum balance on the fluid flow as a whole. 

Petersen [12] points out that this criterion is invalid for more complex chemical reactions whose rate is retarded by products. In such cases, the observed kinetic rate expression should be substituted into the material balance equation for the particular geometry of particle concerned. An asymptotic solution to the material balance equation then gives the correct form of the effectiveness factor. The results indicate that the inequality (23) is applicable only at high partial pressures of product. For low partial pressures of product (often the condition in an experimental differential tubular reactor), the criterion will depend on the magnitude of the constants in the kinetic rate equation. 

This is the differential form of the mass balance equation in three dimensions. Since J can be written as pu, where u is the flow velocity of the fluid, the above equation can also be written as... 

The computer-reconstructed catalyst is represented by a discrete volume phase function in the form of 3D matrix containing information about the phase in each volume element. Another 3D matrix defines the distribution of active catalytic sites. Macroporosity, sizes of supporting articles and the correlation function describing the macropore size distribution are evaluated from the SEM images of porous catalyst (Koci et al., 2006 Kosek et al., 2005). Spatially 3D reaction-diffusion system with low concentrations of reactants and products can be described by mass balances in the form of the following partial differential equations (Koci et al., 2006, 2007a). For gaseous components ... 

The differential rate equations for the concentration of A and for the temperature within the reactor (the mass- and heat-balance equations) can be written in the form... 

All balance equations are put in a more amenable form by dividing them by the differential volume, AxAyAz, and putting them in terms per unite volume,... 

This allows us to represent partial differential equations as found in the balance equations using the collocation method. Equation (11.47) is a solution to a partial differential equation represented by a system of linear algebraic equations, formed by the interpolation coefficients, oij, and the operated radial functions. The interpolation coefficients are solved for using matrix inversion techniques to approximately satisfy the partial differential equation... 

It should be understood that this rate expression may in fact represent a set of diffusion and mass transfer equations with their associated boundary conditions, rather than a simple explicit expression. In addition one may write a differential heat balance for a column element, which has the same general form as Eq. (17), and a heat balance for heat transfer between particle and fluid. In a nonisothermal system the heat and mass balance equations are therefore coupled through the temperature dependence of the rate of adsorption and the adsorption equilibrium, as expressed in Eq. (18). 

The quantity of most immediate interest with respect to the steady-state flow fluid in a straight length of pipe is the pressure change accompanying flow. Th appropriate equation for this calculation is Eq. (7.11), the mechanical-energ balance. To allow for the continuous change of properties ih a flowing fluid, w write Eq. (7.11) in differential form ... 

The macroscopic approach, in which it is not taken into account what happens inside the cell in detail, but only an overall view of the system is described. In fact, the system is considered as a black box from the fluid dynamic point of view and then, it is assumed that the cell behaves a mixed tank reactor (the values of the variables only depend on time and not on the position since only one value of every variable describes all positions). This assumption allows simplifying directly all the set of partial differential equations to an easier set of differential equations, one for each model species. For the case of a continuous-operation electrochemical cell, the mass balances take the form shown in (4.5), where [.S, ]... 

The balance equations (7.12 and 7.13) form a set of coupled ordinary differential equations, which has to be solved numerically. Analytical integration is possible for special cases only. 

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