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Interfaces moving interface problems

Transcendental equations, such as for A in Eq. 20.10, appear frequently in moving interface problems and can be solved using numerical methods. [Pg.504]

Li Z (1997) Immersed interface methods for moving interface problems. Numerical Algorithms 14 269-293... [Pg.357]

Steven G (1982) Internally Discontinuous Finite elements for moving interface problems. Int J Numer Methods Eng 18 (4), 569-582... [Pg.372]

Conduction with Change of Phase A special type of transient problem (the Stefan problem) involves conduction of heat in a material when freezing or melting occurs. The liquid-solid interface moves with time, and in addition to conduction, latent heat is either generated or absorbed at the interface. Various problems of this type are discussed by Bankoff [in Drew et al. (eds.). Advances in Chemical Engineering, vol. 5, Academic, New York, 1964]. [Pg.557]

The direct-liquid-introduction (DLI) interface was made available commercially just after the moving-belt interface to which, as no company produced both types, it was an alternative. At this time, therefore, the commercial LC-MS interface used within a laboratory was dictated by the manufacturer of the mass spectrometer already in use unless a new instrument was being purchased solely for LC-MS applications. The development of LC-MS in the early 1980s was such that this was very rare and it was therefore unusual that a scientific evaluation was carried out to assess the ability of a type of interface to solve problems within a particular laboratory. [Pg.140]

Denote boundary motion speed as u that may or may not depend on time. For crystal growth, the interface moves to the right with x = Xo>0. For crystal dissolution, the interface moves to the left with x = Xo<0. That is, u is positive during crystal growth and negative during crystal dissolution under our setup of the problem. The interface position can be found as... [Pg.274]

Normally, it is not possible to obtain analytical solutions for this transport problem and so we cannot a priori calculate the reaction path. Kirkaldy [J. S. Kirkaldy, D. J. Young (1985)] did pioneering work on metal systems, based on investigations by C. Wagner and the later work of Mullins and Sekerka. They used the diffusion path concept to formulate a number of stability rules. These rules can explain the facts and are predictive within certain limits if applied properly. One of Kirkaldy s results is this. The moving interface in a ternary system is morphologically stable if... [Pg.284]

In the moving-boundary problems treated above, it was assumed that the interface retained its basic initial shape as it moved. It is important to realize that such problems are a subset of a much wider class of problems known as free-boundary problems, in which the boundary is allowed to change its shape as a function of time [2]. A mathematically correct solution for the motion of a boundary of a fixed ideal shape is no guarantee that it is physically realistic. [Pg.515]

With adiabatic combustion, departure from a complete control of m by the gas-phase reaction can occur only if the derivation of equation (5-75) becomes invalid. There are two ways in which this can happen essentially, the value of m calculated on the basis of gas-phase control may become either too low or too high to be consistent with all aspects of the problem. If the gas-phase reaction is the only rate process—for example, if the condensed phase is inert and maintains interfacial equilibrium—then m may become arbitrarily small without encountering an inconsistency. However, if a finite-rate process occurs at the interface or in the condensed phase, then a difficulty arises if the value of m calculated with gas-phase control is decreased below a critical value. To see this, consider equation (6) or equation (29). As the value of m obtained from the gas-phase analysis decreases (for example, as a consequence of a decreased reaction rate in the gas), the interface temperature 7], calculated from equation (6) or equation (29), also decreases. According to equation (37), this decreases t. Eventually, at a sufficiently low value of m, the calculated value of T- corresponds to Tj- = 0, As this condition is approached, the gas-phase solution approaches one in which dT/dx = 0 at x = 0, and the reaction zone moves to an infinite distance from the interface. The interface thus becomes adiabatic, and the gas-phase processes are separated from the interface and condensed-phase processes. [Pg.245]

Whilst the object of this chapter has been to show the extent and type of HPLC technique that is used today in today s environmental laboratories, there are a number of less routine techniques that may or may not have an impact on routine environmental monitoring. One of the most potentially important of these is the use of LC-MS. The problems associated with using LC-MS for trace analysis are twofold one is the usual LC-MS problem of interfacing the second is that of sensitivity of detector. The interfacing problem may well continue to have partial (compared with GC-MS interfacing) solutions such as FAB, and thermospray, etc. However, even given the advances arising from electrospray interfaces the answer may well be to move away from LC-MS to supercritical fluids and SFC-MS. [Pg.246]

Pore Mouth (or Shell Progressive) Poisoning This mechanism occurs when the poisoning of a pore surface begins at the mouth of the pore and moves gradmuly inward. This is a moving boundary problem, and the pseudo-steady-state assumption is made that the boundary moves slowly compared with diffusion of poison and reactants and reaction on the active surface. P is the fraction of the pore that is deactivated. The poison diffuses through the dead zone and deposits at the interface between the dead and active zones. The reactants diffuse across the dead zone without reaction, followed by diffusion-reaction in the active zone. [Pg.23]


See other pages where Interfaces moving interface problems is mentioned: [Pg.877]    [Pg.4]    [Pg.118]    [Pg.507]    [Pg.295]    [Pg.3]    [Pg.4]    [Pg.6]    [Pg.283]    [Pg.353]    [Pg.297]    [Pg.252]    [Pg.261]    [Pg.276]    [Pg.277]    [Pg.502]    [Pg.508]    [Pg.78]    [Pg.85]    [Pg.86]    [Pg.112]    [Pg.116]    [Pg.202]    [Pg.18]    [Pg.88]   
See also in sourсe #XX -- [ Pg.118 , Pg.119 ]




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