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Efficiency packed columns

Strigle [139] discusses packed column efficiency (HETP) in considerable detail. Most of his published data refers to work of Norton Chemical Process Products Corp. [Pg.378]

Eckert [9] showed that a relative height equivalent to a theoretical stage (HETS) vs. the dispersed-phase velocity revealed the packed-column efficiency, or simply the required height, to make one theoretical stage. (See Fig. 7.10). Eckert and others [6, 8] have shown that normally the theoretical packed-column stage requires 2.5 ft of column packed height. All this of course refers strictly to liquid-liquid extraction processing. Also, the continuous-phase velocity Vc (ft/h) and the dispersed-phase velocity VD (ft/h) are referenced to the liquid-phase... [Pg.283]

L/V ratio. Most packed-column efficiency testing has been at total reflux, Some testB for both random (3,61,115) and structured packings (3,32,116) suggest that efficiencies at finite reflux are similar to those at total reflux. [Pg.526]

The results of investigating the dynamics of ion exchange (see Sec. VI) show that the lowest value of HETP or HTU is obtained by exchange of ions in a dense bed. When the bed is less densely packed column efficiency is decreased. [Pg.72]

As is the case for a tray column, the efficiency depends on the system properties, the flow conditions, and the geometry of the device. Because of the many possible variations in the geometry of the packed bed, the last-named parameter assumes great importance in the estimation of packed column efficiency. [Pg.324]

Methods for predicting efficiency also parallel those for tray columns comparison against a similar installation, use of empirical methods, direct scaleup from laboratory or pilot plant, and use of theoretically derived models. Approaches by vendors of packing usually center on comparisons with similar installations (the so-called vendor experience ) and empirical approximations. Direct scaleup from small column studies is difficult with packed columns because of the unknown effects of geometrical factors and the variations of liquid distribution that are required for practical reasons. Theoretical or semitheoretical models are difficult to validate because of the flow effects on interfacial area. It may be concluded that there is no veiy good way to predict packed column efficiency, at least for the random type packings. [Pg.324]

In the case of a plate column the performance of a real plate is related to the performance of a theoretical one by the plate efficiency. In the case of a packed column the height equivalent to a theoretical plate HETP) gives a measure of the contacting efficiency of the packing. [Pg.393]

To minimize the multiple path and mass transfer contributions to plate height (equations 12.23 and 12.26), the packing material should be of as small a diameter as is practical and loaded with a thin film of stationary phase (equation 12.25). Compared with capillary columns, which are discussed in the next section, packed columns can handle larger amounts of sample. Samples of 0.1-10 )J,L are routinely analyzed with a packed column. Column efficiencies are typically several hundred to 2000 plates/m, providing columns with 3000-10,000 theoretical plates. Assuming Wiax/Wiin is approximately 50, a packed column with 10,000 theoretical plates has a peak capacity (equation 12.18) of... [Pg.564]

Microcolumns use less solvent and, because the sample is diluted to a lesser extent, produce larger signals at the detector. These columns are made from fused silica capillaries with internal diameters of 44—200 pm and lengths of up to several meters. Microcolumns packed with 3-5-pm particles have been prepared with column efficiencies of up to 250,000 theoretical plates. [Pg.579]

Open tubular microcolumns also have been developed, with internal diameters of 1-50 pm and lengths of approximately 1 m. These columns, which contain no packing material, may be capable of obtaining column efficiencies of up to 1 million theoretical plates.The development of open tubular columns, however, has been limited by the difficulty of preparing columns with internal diameters less than 10 pm. [Pg.579]

Nonisothermal Gas Absorption. The computation of nonisothermal gas absorption processes is difficult because of all the interactions involved as described for packed columns. A computer is normally required for the enormous number of plate calculations necessary to estabUsh the correct concentration and temperature profiles through the tower. Suitable algorithms have been developed (46,105) and nonisothermal gas absorption in plate columns has been studied experimentally and the measured profiles compared to the calculated results (47,106). Figure 27 shows a typical Hquid temperature profile observed in an adiabatic bubble plate absorber (107). The close agreement between the calculated and observed profiles was obtained without adjusting parameters. The plate efficiencies required for the calculations were measured independendy on a single exact copy of the bubble cap plates installed in the five-tray absorber. [Pg.42]

Pulsed Columns. The efficiency of sieve-plate or packed columns is increased by the appHcation of sinusoidal pulsation to the contents of the column. The weU-distributed turbulence promotes dispersion and mass transfer while tending to reduce axial dispersion in comparison with the unpulsed column. This leads to a substantial reduction in HETS or HTU values. [Pg.75]

Removal of Refractory Organics. Ozone reacts slowly or insignificantly with certain micropoUutants in some source waters such as carbon tetrachloride, trichlorethylene (TCE), and perchlorethylene (PCE), as well as in chlorinated waters, ie, ttihalomethanes, THMs (eg, chloroform and bromoform), and haloacetic acids (HAAs) (eg, trichloroacetic acid). Some removal of these compounds occurs in the ozone contactor as a result of volatilization (115). Air-stripping in a packed column is effective for removing some THMs, but not CHBr. THMs can be adsorbed on granular activated carbon (GAG) but the adsorption efficiency is low. [Pg.502]

Design data for separation of the particular or similar mixture in a packea column are not available. Design procedures are better estabhshed for tray-type columns than for packed columns. This is particularly so with respect to separation efficiency since tray efficiency can be estimated more accurately than packed height equivalent to a theoretical stage (HETP). [Pg.1346]

Selection of Equipment Packed columns usually are chosen for very corrosive materials, for liquids that foam badly, for either small-or large-diameter towers involving veiy low allowable pressure drops, and for small-scale operations requiring diameters of less than 0.6 m (2 ft). The type of packing is selected on the basis of resistance to corrosion, mechanical strength, capacity for handling the required flows, mass-transfer efficiency, and cost. Economic factors are discussed later in this sec tion. [Pg.1352]

FIG. 14-47 Efficiency characteristics of packed columns (total-reflux distillation.)... [Pg.1387]

For total-reflux distillations carried out in packed columns, regions of loading and flooding are identified by their effects on mass-transfer efficiency, as shown in Fig. 14-47. Gas and liquid rate increase... [Pg.1387]

FIG. 23-38 Efficiency and capacity range of small-diameter extractors, 50 to 150 mm diameter. Acetone extracted from water with toluene as the disperse phase, V /V = 1.5. Code AC = agitated cell PPC = pulsed packed column PST = pulsed sieve tray RDC = rotating disk contactor PC = packed column MS = mixer-settler ST = sieve tray. (Stichlmair, Chem. Ing. Tech. 52(3), 253-255 [1980]). [Pg.2118]


See other pages where Efficiency packed columns is mentioned: [Pg.67]    [Pg.1219]    [Pg.469]    [Pg.1620]    [Pg.132]    [Pg.970]    [Pg.1055]    [Pg.324]    [Pg.1616]    [Pg.1400]    [Pg.526]    [Pg.67]    [Pg.1219]    [Pg.469]    [Pg.1620]    [Pg.132]    [Pg.970]    [Pg.1055]    [Pg.324]    [Pg.1616]    [Pg.1400]    [Pg.526]    [Pg.565]    [Pg.579]    [Pg.615]    [Pg.74]    [Pg.476]    [Pg.501]    [Pg.170]    [Pg.171]    [Pg.171]    [Pg.173]    [Pg.1292]    [Pg.1313]    [Pg.1346]    [Pg.1434]    [Pg.2003]    [Pg.2118]   
See also in sourсe #XX -- [ Pg.56 ]

See also in sourсe #XX -- [ Pg.15 , Pg.46 , Pg.50 ]




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