Transfer longitudinal

Longitudinal fins can also be used, but their application is restricted to small heat exchangers in the form of a concentric pipe heat exchanger, similar to the schematic in Figure 15.5a. In this arrangement, the inner tube would be the extended surface tube with the fins in the annular space to enhance the heat transfer. Longitudinal fins can increase the surface area by a factor of 14 to 20 relative to plain tubes. 

In Debye solvents, x is tire longitudinal relaxation time. The prediction tliat solvent polarization dynamics would limit intramolecular electron transfer rates was stated tlieoretically [40] and observed experimentally [41]. 

Schematics illustrating the contributions to band broadening due to (a) multiple paths, (b) longitudinal diffusion, and (c) mass transfer.

To determine how the height of a theoretical plate can be decreased, it is necessary to understand the experimental factors contributing to the broadening of a solute s chromatographic band. Several theoretical treatments of band broadening have been proposed. We will consider one approach in which the height of a theoretical plate is determined by four contributions multiple paths, longitudinal diffusion, mass transfer in the stationary phase, and mass transfer in the mobile phase. 

To increase the number of theoretical plates without increasing the length of the column, it is necessary to decrease one or more of the terms in equation 12.27 or equation 12.28. The easiest way to accomplish this is by adjusting the velocity of the mobile phase. At a low mobile-phase velocity, column efficiency is limited by longitudinal diffusion, whereas at higher velocities efficiency is limited by the two mass transfer terms. As shown in Figure 12.15 (which is interpreted in terms of equation 12.28), the optimum mobile-phase velocity corresponds to a minimum in a plot of H as a function of u. 

Kovat s retention index (p. 575) liquid-solid adsorption chromatography (p. 590) longitudinal diffusion (p. 560) loop injector (p. 584) mass spectrum (p. 571) mass transfer (p. 561) micellar electrokinetic capillary chromatography (p. 606) micelle (p. 606) mobile phase (p. 546) normal-phase chromatography (p. 580) on-column injection (p. 568) open tubular column (p. 564) packed column (p. 564) peak capacity (p. 554)... 

Several wick stmctures are in common use. First is a fine-pore (0.14—0.25 mm (100-60 mesh) wire spacing) woven screen which is roUed into an annular stmcture consisting of one or more wraps inserted into the heat pipe bore. The mesh wick is a satisfactory compromise, in many cases, between cost and performance. Where high heat transfer in a given diameter is of paramount importance, a fine-pore screen is placed over longitudinal slots in the vessel wall. Such a composite stmcture provides low viscous drag for Hquid flow in the channels and a small pore size in the screen for maximum pumping pressure. 

For annuli containing externally Hnned tubes the heat-transfer coefficients are a function of the fin configurations. Knudsen and Katz (Fluid Dynamics and Heat Transfer, McGraw-Hill, New York, 1958) present relationships for transverse finned tubes, spined tubes, and longitudinal finned tubes in annuli. 

Spray Dryers A spray diyer consists of a large cyhndrical and usu ly vertical chamber into which material to be dried is sprayed in the form of small droplets and into which is fed a large volume of hot gas sufficient to supply the heat necessary to complete evaporation of the liquid. Heat transfer and mass transfer are accomphshed by direct contact of the hot gas with the dispersed droplets. After completion of diying, the cooled gas and solids are separated. This may be accomplished partially at the bottom of the diying chamber by classification and separation of the coarse dried particles. Fine particles are separated from the gas in external cyclones or bag collectors. When only the coarse-particle fraction is desired for fini ed product, fines may be recovered in wet scrubbers the scrubber liquid is concentrated and returned as feed to the diyer. Horizontal spray chambers are manufactured with a longitudinal screw conveyor in the bottom of the diying chamber for continuous removal of settled coarse particles. 

A horizontally fired burner is located at one end of the heater. The flame extends along the central longitudinal axis of the heater. In this way the wickets are exposed to the open flame and can be subjected to a maximum rate of radiant heat transfer. The tubes should be sufficiently far away from the flame to prevent hot spots or flame pinching. 

Various mathematical concepts and techniques have been used to derive the functions that describe the different types of dispersion and to simplify further development of the rate theory two of these procedures will be discussed in some detail. The two processes are, firstly, the Random Walk Concept [1] which was introduced to the rate theory by Giddings [2] and, secondly, the mathematics of diffusion which is both critical in the study of dispersion due to longitudinal diffusion and that due to solute mass transfer between the two phases. The random walk model allows the relatively simple derivation of the variance contributions from two of the dispersion processes that occur in the column and, so, this model will be the first to be discussed. 

Diffusion plays an important part in peak dispersion. It not only contributes to dispersion directly (i.e., longitudinal diffusion), but also plays a part in the dispersion that results from solute transfer between the two phases. Consider the situation depicted in Figure 4, where a sample of solute is introduced in plane (A), plane (A) having unit cros-sectional area. Solute will diffuse according to Fick s law in both directions ( x) and, at a point (x) from the sample point, according to Ficks law, the mass of solute transported across unit area in unit time (mx) will be given by... 

The dispersion of a solute band in a packed column was originally treated comprehensively by Van Deemter et al. [4] who postulated that there were four first-order effect, spreading processes that were responsible for peak dispersion. These the authors designated as multi-path dispersion, longitudinal diffusion, resistance to mass transfer in the mobile phase and resistance to mass transfer in the stationary phase. Van Deemter derived an expression for the variance contribution of each dispersion process to the overall variance per unit length of the column. Consequently, as the individual dispersion processes can be assumed to be random and non-interacting, the total variance per unit length of the column was obtained from a sum of the individual variance contributions. 

The curves represent a plot of log (h ) (reduced plate height) against log (v) (reduced velocity) for two very different columns. The lower the curve, the better the column is packed (the lower the minimum reduced plate height). At low velocities, the (B) term (longitudinal diffusion) dominates, and at high velocities the (C) term (resistance to mass transfer in the stationary phase) dominates, as in the Van Deemter equation. The best column efficiency is achieved when the minimum is about 2 particle diameters and thus, log (h ) is about 0.35. The optimum reduced velocity is in the range of 3 to 5 cm/sec., that is log (v) takes values between 0.3 and 0.5. The Knox... 

Now, at high linear velocities, the longitudinal diffusion term will become insignificant and, equally important, the resistance to mass transfer term that incorporates the inverse function of diffusivity will become large, thus improving the precision of measurement. 

Dispersion equations, typically the van Deemter equation (2), have been often applied to the TLC plate. Qualitatively, this use of dispersion equations derived for GC and LC can be useful, but any quantitative relationship between such equations and the actual thin layer plate are likely to be fraught with en or. In general, there will be the three similar dispersion terms representing the main sources of spot dispersion, namely, multipath dispersion, longitudinal diffusion and dispersion due to resistance to mass transfer between the two phases. 

HETP of a TLC plate is taken as the ratio of the distance traveled by the spot to the plate efficiency. The same three processes cause spot dispersion in TLC as do cause band dispersion in GC and LC. Namely, they are multipath dispersion, longitudinal diffusion and resistance to mass transfer between the two phases. Due to the aforementioned solvent frontal analysis, however, neither the capacity ratio, the solute diffusivity or the solvent velocity are constant throughout the elution of the solute along the plate and thus the conventional dispersion equations used in GC and LC have no pertinence to the thin layer plate. 

The dummy tubes do not pass through the tubesheets, and can be located close to the inside of the shell. The seating strips extend from baffle to baffle in a longitudinal direction and effectively channel the fluid across the tubes to minimize turbulence and heat transfer. On some fixed tubesheet designs, the outer tubes are in close proximity to the inside of the shell so that by-pass is minimal and no by-pass elimination is necessary. There are a number of... 

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