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Diffusion operator

The optimum pressure level for gaseous diffusion operation is also determined by comparison at some pressure level the decrease ia equipment size and volume to be expected from increasing the pressure and density is outweighed by the losses that occur ia the barrier efficiency. Nevertheless, because it is weU known that the cost of power constitutes a large part of the total cost of operation of gaseous diffusion plants, it can perhaps be assumed that a practical value of r does not differ gready from the above optimum. Inclusion of this value ia the preceding equations yields... [Pg.87]

Combined Intraparticle Resistances When solid diffusion and pore diffusion operate in parallel, the effec tive rate is the sum of these two rates. When solid diffusion predominates, mass transfer can be represented approximately in terms of the LDF approximation, replacing/c in column 2 of Table 16-12 with... [Pg.1514]

In the case of dilute polymer solutions, L is conventionally taken to be the Kirkwood-Riseman diffusion operator [99]. As a consequence, the generalized mobility p(Q)... [Pg.71]

Diffusion operates along well-defined physical principles first described in 1855 by Adolf Fick and now widely known as Fick s Laws of Diffusion. Philbert5 provides a detailed explanation of the laws and a historical account of Fick. While they were designed to describe the behavior of gas molecules under ideal theoretical conditions, Fick s Laws serve reasonably well to describe a wide variety of real diffusion events. Fick wrote the laws as a set of equations in the language of calculus but these can be rephrased in plain English. [Pg.197]

P(Qol, t) is the conditional probability of the orientation being at time t, provided it was Qq a t time zero. The symbol — F is the rotational diffusion operator. In the simplest possible case, F then takes the form of the Laplace operator, acting on the Euler angles ( ml) specifying the orientation of the molecule-fixed frame with respect to the laboratory frame, multiplied with a rotational diffusion coefficient. Dr. Equation (44) then becomes identical to the isotropic rotational diffusion equation. The rotational diffusion coefficient is simply related to the rotational correlation time introduced earlier, by tr = 1I6Dr. [Pg.65]

Here we no longer have molecular diffusion operating exclusively ( ) and the diffusion coefficient, frictional factor and chemical potential are no longer Interrelated. Also, the energy dissipation function is probably no longer quadratic. For simplicity, at unit rejection, for the steady state... [Pg.163]

The N terms in the diffusion operator (Sano and Baird s [504] M operator) can be retained because Piv-i.jw-i does not retain any dependence on rfe, so the term in Vft, etc. is zero. In the reactive sink term, the overlap of the kv pair, S/ v must be removed. However, it could have been taken to the right-hand side as a source term and represented as feact/d r0 9 vnbii M. There are (N — 1) (M — 1) such equations and N — 2) (M — 2) equations involving the survival probability Pat-2,m-2> when derived from an initial cluster of N anions and M cations. The sum total of all the probabilities that a particular distribution exists at a time f0, is... [Pg.298]

In considering the case of maximum release, it is apparent that complete mixing in the liquid phase will lead to a greater release rate than that expected in cases where diffusion operates in two phases. Therefore, consider the case where both the solvent (Na) and the solute (volatile fission product) diffuse through a gas layer of constant thickness. It follows from the solution to Fick s law with appropriate boundary conditions that... [Pg.82]

But wet steam is bad for a jet, even when it does not cause the jet to freeze. Mainly, wet steam causes erosion of the steam inlet nozzle. Erosion of this nozzle is the main reason why jets undergo mechanical deterioration. As the nozzle erodes, it allows more steam to pass through into the diffuser. The diameter of the diffuser is designed to operate with a certain steam flow. If that design steam flow is exceeded, the diffuser operation suffers. Also, the downstream condenser pressure will also increase. [Pg.198]

The spin-lattice relaxation process is usually exponential. Theoretically, the effect of spin-diffusion, characterized by the coefficient D (order of 1(T12 cm2 s 1), has an influence on T, relaxation times when ix > L2/D, where Lis the diffusion path length. NMR studies of model systems f6r rubber networks, based on a styrene-butadiene-styrene block copolymer (SBSy, in which styrene blocks act as a crosslink for polybutadiene rubber segments of known and uniform length, indicate that spin diffusion operating between PS and PB phases causes a lowering of Tg for the PS component in SBS (as compared to the pure PS) and hindering of the motion of the PB component (as compared to the pure PB)51). [Pg.21]

The formation of the steady-state recombination profile (4.1.62) occurs for the space dimension d = 3 only. For instance, if d = 2, taking into account the change in the diffusion operator A and the expression for the two-dimensional reaction rate... [Pg.185]

Here the diffusion operator DA is replaced by the operator L describing motion as stochastic hops in the continuous coordinate space. Let distribution function of hop lengths normalized as... [Pg.207]

FIG. 14-95 Comparison of bubbles from a porous septum and from a perforated-pipe sparger. Air in water at 70°F. (a) Grade 25 porous-carbon diffuser operating under a pressure differential of 13.7 in of water, (b) Karbate pipe perforated with 1/16-in holes on 1-in centers. To convert inches to centimeters, multiply by 2.54 °C = SA (°F - 32). (National Carbon Co.)... [Pg.105]

Regarding the application of the second potential step U i I l2 0 < t2 < r2), due to that the diffusion operator for spherical diffusion is linear, the solutions of the differential equation system can be written as... [Pg.628]

In Figure 2.10 we show a selection of results, in which experimental and calculated spectra are compared at 292 and 155K. The results are quite satisfactory, especially when considering that no fitted parameters, but only calculated quantities (via QM and hydrodynamic models) have been employed. The overall satisfactory agreement of the spectral line shapes, particularly at low temperatures, is a convincing proof that the simplified dynamic modelling implemented in the SLE through the purely rotational stochastic diffusive operator f, and the hydrodynamic calculation of the rotational diffusion tensor, is sufficient to describe the main slow relaxation processes. [Pg.163]

The same rate law was obeyed for silica gels with pore radii changing from 2.3 to 40 nm.42 This similarity of the kinetic data for silicas with very different textures, showed diffusion operating mechanisms not to play a determining role. [Pg.340]

From the values of A listed in Table 4.1, only the two extreme values 0.5 and 1.0 for thin films (or slabs) have a physical meaning. When A = 0.5, pure Fickian diffusion operates and results in diffusion-controlled drug release. It should be recalled here that the derivation of the relevant (4.3) relies on short-time approximations and therefore the Fickian release is not maintained throughout the release process. When A = 1.0, zero-order kinetics (Case II transport) are justified in accord with (4.4). Finally, the intermediate values of A (cf. the inequalities in Table 4.1) indicate a combination of Fickian diffusion and Case II transport, which is usually called anomalous transport. [Pg.64]

Skaggs and Kabala [59] employed the QR method for the same problem solved in their TR method. In the QR method, Skaggs and Kabala solved an equation that is close to the original equation and that is stable with a negative time step. The diffusion operator... [Pg.86]

The first approach is the discretization of the convection and the diffusion operators of the PDEs, which gives rise to a large (or very large) system of effective low-dimensional models. The order of these low-dimensional models depend on the minimum mesh size (or discretization interval) required to avoid spurious solutions. For example, the minimum number of mesh points (Nxyz) necessary to perform a direct numerical simulation (DNS) of convective-diffusion equation for non-reacting turbulent flow is given by (Baldyga and Bourne, 1999)... [Pg.214]

We note that the diffusion operator with Neumann (or periodic) boundary conditions is symmetric and has a simple zero eigenvalue with a constant eigenfunction. Equivalently, the eigenvalue problem... [Pg.218]

FIG. 14-95a Comparison of bubbles from a porous septum and from a perforated-pipe sparger. Air in water at 70°F. Grade 25 porous-carbon diffuser operating under a pressure differential of 13.7 in of water. [Pg.1243]

Emissions are independent of the tracer concentration and can be considered as a surface flux. The injection of the emissions is integral part of the diffusion scheme in MOZART-3, i.e. as lower boundary for the fluxes, whereas TM5 and MOCAGE distribute the injected mass in a fixed ratio over selected layers in the boundary layer and apply their diffusion operator after the injection. The tendencies of the emissions P, therefore, have to be formulated either as 3D field including the diffusion or as 2D flux term. The diffusion in the IFS would have to be switched off if the 3D emissions-diffusion tendencies are applied. Air bom emissions such as the ones from aircraft would have to be included in the 3D chemistry tendencies, if the surface emissions are expressed as a flux. [Pg.117]

We have derived Eq. (11-36) with mixing of the singlet and triplet states of a radical pair in mind, but it is quite general for the time evolution of two levels separated by an energy under a stationary perturbation. In order to get the dynamic behavior of a radical pair, we should add a diffusion operator D and an operator K for the chemical reaction to Eq. (11-29),... [Pg.161]

We will assume the mesophase director to be parallel to the direction of the static magnetic field. In the last section, III.E, the no-inertia assumption will be rejected and the diffusion operator (2.6) replaced with the complete Hubbard operator. We shall investigate the spectroscopic effects of molecular inertia in the case of an axially symmetric g-tensor. [Pg.334]


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See also in sourсe #XX -- [ Pg.367 ]

See also in sourсe #XX -- [ Pg.214 ]




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