Big Chemical Encyclopedia

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

Articles Figures Tables About

Partial differential across

Membranes act as a semipermeable barrier between two phases to create a separation by controlling the rate of movement of species across the membrane. The separation can involve two gas (vapor) phases, two liquid phases or a vapor and a liquid phase. The feed mixture is separated into a retentate, which is the part of the feed that does not pass through the membrane, and a permeate, which is that part of the feed that passes through the membrane. The driving force for separation using a membrane is partial pressure in the case of a gas or vapor and concentration in the case of a liquid. Differences in partial pressure and concentration across the membrane are usually created by the imposition of a pressure differential across the membrane. However, driving force for liquid separations can be also created by the use of a solvent on the permeate side of the membrane to create a concentration difference, or an electrical field when the solute is ionic. [Pg.193]

Export processes are often more complicated than the expression given in Equation 7, for many chemicals can escape across the air/water interface (volatilize) or, in rapidly depositing environments, be buried for indeterminate periods in deep sediment beds. Still, the majority of environmental models are simply variations on the mass-balance theme expressed by Equation 7. Some codes solve Equation 7 directly for relatively large control volumes, that is, they operate on "compartment" or "box" models of the environment. Models of aquatic systems can also be phrased in terms of continuous space, as opposed to the "compartment" approach of discrete spatial zones. In this case, the partial differential equations (which arise, for example, by taking the limit of Equation 7 as the control volume goes to zero) can be solved by finite difference or finite element numerical integration techniques. [Pg.34]

Packer fluids are used to provide hydrostatic balance to partially offset the reservoir pressure and eliminate a large pressure differential across the packer element. TKPP solutions more than meet the requirements of being noncorrosive, nondestructive to elastomers, variable in density, and stable for many years. It is desirable to perforate with a well bore filled with packer fluid so that the packer can be set and the well produced as soon as the perforation operation is complete. Since TKPP solutions make superior perforation fluids, their dual use as a packer fluid is further enhanced. [Pg.634]

It is impossible to read much of the literature on viscosity without coming across some reference to the equation of motion. In the area of fluid mechanics, this equation occupies a place like that of the Schrodinger equation in quantum mechanics. Like its counterpart, the equation of motion is a complicated partial differential equation, the analysis of which is a matter for fluid dynamicists. Our purpose in this section is not to solve the equation of motion for any problem, but merely to introduce the physics of the relationship. Actually, both the concentric-cylinder and the capillary viscometers that we have already discussed are analyzed by the equation of motion, so we have already worked with this result without explicitly recognizing it. The equation of motion does in a general way what we did in a concrete way in the discussions above, namely, describe the velocity of a fluid element within a flowing fluid as a function of location in the fluid. The equation of motion allows this to be considered as a function of both location and time and is thus useful in nonstationary-state problems as well. [Pg.158]

In this case, the potential drop across the electrode structure is related by the six dimensionless parameters ju, s, a, y as well as the aspect ratio Q and Peclet number/5 that character the convection in the axial direction. It is possible to approximately analyze this generalized theoretical nonlinear model using the set of partial differential equations with boundary conditions by ADM.22... [Pg.292]

The film diffusion process assumes that reactive surface groups are exposed directly to the aqueous-solution phase and that the transport barrier to adsorption involves only the healing of a uniform concentration gradient across a quiescent adsorbent surface boundary layer. If instead the adsorbent exhibits significant microporosity at its periphery, such that aqueous solution can effectively enter and adsorptives must therefore traverse sinuous microgrottos in order to reach reactive adsorbent surface sites, then the transport control of adsorption involves intraparticle diffusion.3538 A simple mathematical description of this process based on the Fick rate law can be developed by generalizing Eq. 4.62 to the partial differential expression36... [Pg.169]

The boundary layer integral equations have been derived above without recourse to the partial differential equations for boundary layer flow. They can, however, be determined directly from these equations. Consider, for example, the laminar momentum equation (2.140). Integrating this equation across the boundary layer to some distance from the wall, i being greater than the boundary layer thickness, gives because du/dy is zero outside the boundary layer and because dp/dx is independent of y ... [Pg.78]

The solution of the above system of partial differential equations (eqs 4-12) yields the concentration and temperature profiles inside the catalyst pellet, and if necessary across the external boundary layer, as a function of time. However, there are only few cases of practical importance where this complete solution is required, as for instance startup and shutdown periods, dynamic process control options such as the so-called Matros concept with flow reversals (for redox processes), or situations where the catalyst is rapidly deactivated. [Pg.329]

The upper parts of Fig. 7.7 show this initial policy for a and corresponding ge it can be shown that ge has a continuous derivative and this amply assures the existence of the solution of the partial differential equation (20). Any characteristic emanating from the region (I) starts with a = a and maintains this value until the right-hand side of (19) reaches a. Since it is a region of constant temperature the solution (28) applies and we can determine the arc BD across which a increases above a analytically it is... [Pg.150]

Mathematical modeling of mass or heat transfer in solids involves Pick s law of mass transfer or Fourier s law of heat conduction. Engineers are interested in the distribution of heat or concentration across the slab, or the material in which the experiment is performed. This process is represented by parabolic partial differential equations (unsteady state) or elliptic partial differential equations. When the length of the domain is large, it is reasonable to consider the domain as semi-infinite which simplifies the problem and helps in obtaining analytical solutions. These partial differential equations are governed by the initial condition and the boundary condition at x = 0. The dependent variable has to be finite at distances far (x = ) from the origin. Both parabolic and elliptic partial... [Pg.295]

Chromatographic separation is achieved by selective adsorption of chemical species in a packed column. Consider a one-dimensional, isothermal chromatographic column, which is fed with a mixture of m-species at axial velocity v, uniform across the cross-section. Let C be the moles per unit volume concentration of species i in liquid phase, and be the concentration of the species in the moles per unit volume. The local mass balances for each of the species result in the following set of first-order partial differential equations (Rhee et al., 1986) ... [Pg.49]

Because the simulations use code-based, reduced-order models instead of FEM-based or BEM-based partial differential equation models, the simulation time is reduced by orders of magnitude. The compelling benefit of this new paradigm is twofold (1) designers can capture complete device and subsystem behavior across the different physics domains required for sensor, optical, and RF MEMS, and (2) accurate, comprehensive simulations take only minutes instead of days, enabling rapid exploration of wide-ranging design spaces. [Pg.64]

In laminar flow, heat transfer occurs only by conduction, as there are no eddies to carry heat by convection across an isothermal surface. The problem is amenable to mathematical analysis based on the partial differential equations for continuity, momentum, and energy. Such treatments are beyond the scope of this book and are given in standard treatises on heat transfer, Mathematical solutions depend on the boundary conditions established to define the conditions of fluid flow and heat transfer. When the fluid approaches the heating surface, it may have an already completed hydrodynamic boundary layer or a partially developed one. Or the fluid may approach the heating surface at a uniform velocity, and both boimdary layers may be initiated at the same time. A simple flow situation where the velocity is assumed constant in all cross sections and tube lengths is called... [Pg.333]

The origin of this phenomenon can he traced to the drying step of the liquid development process. During the development step, after the resist-patterned wafer has been contacted with the developer solution for a given length of time and subsequently rinsed with deionized water, the level of the rinse liquid at some point attains a condition similar to that shown in Fig. 11.45, where the space between adjacent resist lines is partially filled with fluid. The fluid meniscus exhibits a curvamre due to the differences in pressure across the fluid interface that result from surface tension in the confined space between the resist lines. Tanaka et al. developed a cantilever beam mechanical model for describing pattern collapse. The Laplace equation relates the pressure differential across the meniscus... [Pg.532]


See other pages where Partial differential across is mentioned: [Pg.2592]    [Pg.378]    [Pg.456]    [Pg.151]    [Pg.32]    [Pg.501]    [Pg.378]    [Pg.139]    [Pg.453]    [Pg.283]    [Pg.168]    [Pg.260]    [Pg.349]    [Pg.108]    [Pg.352]    [Pg.359]    [Pg.582]    [Pg.367]    [Pg.1074]    [Pg.13]    [Pg.54]    [Pg.260]    [Pg.349]    [Pg.44]    [Pg.19]    [Pg.2592]    [Pg.594]    [Pg.91]    [Pg.460]    [Pg.78]    [Pg.499]    [Pg.511]    [Pg.126]    [Pg.166]    [Pg.236]   


SEARCH



Partial differential

Partial differential across control

© 2024 chempedia.info