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Diffiisional process

The duration of the potential step (the time interval i of Es) is usually determined by the type of information that the experimenter desires of the particular system. The time may vary from as little as 10 /is to as long as several seconds. The minimum time is limited by the ability of the potentiostat to charge the electrode, whereas the maximum time is determined by the onset of convection from vibrations or density gradients. Special shielded electrodes enable times on the order of 100 s to be reached with no apparent disturbance of the diffiisional process. [Pg.54]

The section in Chapter 3 on equilibrium stage separations will include both graphical and analytical techniques. The graphical techniques are useful to visualize the process for the student and the analytical methods reinforce the principles. Rate-based separations will focus on diffiisional processes and convective/dispersive effects which can be described by mass transfer coefficients (k). Initial discussion will focus on which approach to use based on what information is available and what one wants to determine. For analyses using mass transfer coefficients, both the use of correlations to estimate a value for k and the determination of an overall mass transfer coefficient (K) will be covered. [Pg.335]

Inter diffusion diffusion Dab- This is a measure of the rate at which a diffiisional process will occur when ions are interdiffusing. [Pg.225]

A new simple and reliable method for monitoring photoinduced acid generation in polymer films and in solutions of the kind used in 193 nm and deep-UV lithography was developed. By using N-(9-acridinyl)acetamide, a fluorescent acid-sensitive sensor, we have been able to study the effects of trifluoroacetic acid and photoacids generated from triphenylsulfonium hexafluoroantimonate on the spectral properties of the acid sensor in THF solution and in alicyclic polymer resist films exposed at 193 nm. In both cases a hypsochromic spectral shift and an increase in fluorescence intensity were observed upon protonation. This technique could find application in the study of diffiisional processes in thin polymer films. [Pg.190]

The rate-controlling step is no longer a conventional diffiisional process but chemical reaction kinetics are assumed. The rate of ion exchange is governed by the rate constant of the corresponding chemical reaction. Basic laws of chemical kinetics can be used in the mathematical treatment. [Pg.709]

In the paper, a theory for mechanical and diffiisional processes in hyperelastic materials was formulated in terms of the global stress tensor and chemical potentials. The approach described in was used as the basic principle and was generalized to the case of a multi-component mixture. An important feature of the work is that, owing to the structure of constitutive equations, the general model can be used without difficulty to describe specific systems. [Pg.305]

The approaches described previously assume that reactions will be suppressed, without giving any specific mechanism, and then rationalise the behaviour of the process using calculated metastable equilibria. A more innovative approach was taken by Saunders (1984) and Saunders and Miodownik (1985, 1987) for the prediction of phases formed by vapour co-deposition of alloys. It was postulated that the formation of phases on the substrate is controlled by the diffiisional breakdown of iiiUy intermixed depositing atoms so that three kinetic regimes are observed ... [Pg.437]

Oliver, E.D., Diffiisional Separation Processes Theory, Design Evaluation, John Wiley Sons, New York, NY, 1966. [Pg.373]

Beyne and Froment [1993] simulated a tubular reactor with plug flow and diffiisional limitations inside the catalyst for the process discussed already in Section 3. The main reaction is of the type A B and coke is formed through a polymerization mechanism from a site covered by coke... [Pg.65]

In the model employed, bulk diffusion through the grains and diffusion along the grain boundaries must be considered. These two processes are always dominant at low stresses, because the rates of diffiisional flow are usually linear... [Pg.643]

There are a number of models that have been developed for FCS [50]. Generally, in FCS experiments the data are first processed to yield the autocorrelation function as described earlier according to equation 2.15, then a physical model which incorporates descriptions of the sources of fluctuation is used to fit this function allowing the physical parameters of interest to be determined. The simplest case is that of diffiisional motion of a fluorescent particle into and out of the PSF. An analytical expression for the form of the autocorrelation function in the case of a... [Pg.34]

Pick s first law (as well as Pick s second law) can be widely applied to model many diffusion processes in gases, liquids, or solids. The equations do not change between these phases— what changes is the diffusivity. Diffusivities tend to be high in gases, lower in liquids, and very low in solids, thereby capturing the differences in relative speed of diffiisional transport between these three phases of matter. In solids, diffusivities tend to be on the order of 10 -10 cm /s, which means that even diffusion over relatively small distances (e.g., micrometers) can take hours, days, or even longer. A detailed derivation of Pick s first law based on an atomistic picture of diffusion is provided in Section 4.5.3. [Pg.92]

If the support material is initially in the dry state, then the deposition process is called capillary, or dry, impregnation. The speed of pore filling is fast and the process is simple, but there are potential problems of heat release and internal pore collapse due to capillary pressure by entrapped air [18]. If the support is already in contact with the solvent (without the precursor), then the subsequent contact with the precursor solution is known as diffiisional, or wet, impregnation. [Pg.33]

S. SieniutyczandP. Salamon (Eds), F/ow, Diffusion and Rate Processes, Advances in Thermodynamics, o. 6, Taylor Francis, New35>ik (1992). A.H.P. SkeWteaA, Diffiisional Mass Transfer, Krieger Publishing Company, Malabar (1985). [Pg.96]


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