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Packings velocity

With soft gels, column packing has often been plagued with such problems as inferior reproducibility and excessive time requirements. These problems are alleviated with physically stable Toyopearl HW media. However, an improperly packed column can have significantly reduced efficiency. The two key variables for the successful packing of Toyopearl HW media, packing velocity and column size, have been evaluated to determine the optimal packing conditions. [Pg.150]

Figure 4.46 shows the relationship between packing velocity and sample resolution using Toyopearl HW-55F and Toyopearl HW-55S columns and... [Pg.150]

Place the end of the suction tube of the pump in a large container of packing solvent and the outlet tube to waste. Simultaneously open the outlet tube and turn on the pump and pack the column at a starting flow rate of approx. 1/3 of the final packing velocity. [Pg.441]

The most common mobile phases for GC are He, Ar, and N2, which have the advantage of being chemically inert toward both the sample and the stationary phase. The choice of which carrier gas to use is often determined by the instrument s detector. With packed columns the mobile-phase velocity is usually within the range of 25-150 mF/min, whereas flow rates for capillary columns are 1-25 mF/min. Actual flow rates are determined with a flow meter placed at the column outlet. [Pg.563]

Numbers on lines represent G values = gas flow in kg/(m -s) = nominal packing size = superficial velocity. To convert kg/(m -s) to lb/(h-ft )... [Pg.34]

The packing parameter ( ) (m) reflects the influence of the Hquid flow rate as shown in Figure 20. reflects the influence of the gas flow rate, staying at unity below 50% of the flooding rate but beginning to decrease above this point. At 75% of the flooding velocity, = 0.6. Sc is the Schmidt number of the Hquid. [Pg.36]

Pig. 22. Schematic representation of typical pressure drop as a function of superficial gas velocity, expressed in terms of G = /9q tiQ, in packed columns. O, Dry packing , low Hquid flow rate I, higher Hquid flow rate. The points do not correspond to actual experimental data, but represent examples. [Pg.39]

Fig. 16. Plots showing (a) variation of (c F/2)J. / ) with 1 for O2 (left plot, X, 0.84- 0.72 mm = 20-25 mesh Q 0.42-0.29 mm = 40-50 mesh) and N2 (right plot, on 3.2-mm pellets) in Bergbau-Forschung carbon molecular sieve and (b) variation of HETP with Hquid velocity (interstitial) for fmctose (soHd symbols), and glucose (open symbols) in a column packed with KX 2eoHte crystals. From refs. 22 and 23. Fig. 16. Plots showing (a) variation of (c F/2)J. / ) with 1 for O2 (left plot, X, 0.84- 0.72 mm = 20-25 mesh Q 0.42-0.29 mm = 40-50 mesh) and N2 (right plot, on 3.2-mm pellets) in Bergbau-Forschung carbon molecular sieve and (b) variation of HETP with Hquid velocity (interstitial) for fmctose (soHd symbols), and glucose (open symbols) in a column packed with KX 2eoHte crystals. From refs. 22 and 23.
Venturi scmbbers can be operated at 2.5 kPa (19 mm Hg) to coUect many particles coarser than 1 p.m efficiently. Smaller particles often require a pressure drop of 7.5—10 kPa (56—75 mm Hg). When most of the particulates are smaller than 0.5 p.m and are hydrophobic, venturis have been operated at pressure drops from 25 to 32.5 kPa (187—244 mm Hg). Water injection rate is typicaUy 0.67—1.4 m of Hquid per 1000 m of gas, although rates as high as 2.7 are used. Increasing water rates improves coUection efficiency. Many venturis contain louvers to vary throat cross section and pressure drop with changes in system gas flow. Venturi scmbbers can be made in various shapes with reasonably similar characteristics. Any device that causes contact of Hquid and gas at high velocity and pressure drop across an accelerating orifice wiU act much like a venturi scmbber. A flooded-disk scmbber in which the annular orifice created by the disc is equivalent to a venturi throat has been described (296). An irrigated packed fiber bed with performance similar to a... [Pg.410]

In the case of a packed column, the terms on the right-hand side should each be divided by the voidage, ie, the volume fraction not occupied by the soHd packing (71). In unpacked columns at low values of the sHp velocity approximates the terminal velocity of an isolated drop, but the sHp velocity decreases with holdup and may also be affected by column internals such as agitators, baffle plates, etc. The sHp velocity can generally be represented by (73) ... [Pg.69]

Motionless inline mixers obtain energy for mixing and dispersion from the pressure drops developed as the phases flow at high velocity through an array of baffles or packing in a tube. Performance data on the Kenics (132) and Sul2er (133) types of motionless mixer have been reported. [Pg.75]

The basic concepts of a gas-fluidized bed are illustrated in Figure 1. Gas velocity in fluidized beds is normally expressed as a superficial velocity, U, the gas velocity through the vessel assuming that the vessel is empty. At a low gas velocity, the soHds do not move. This constitutes a packed bed. As the gas velocity is increased, the pressure drop increases until the drag plus the buoyancy forces on the particle overcome its weight and any interparticle forces. At this point, the bed is said to be minimally fluidized, and this gas velocity is termed the minimum fluidization velocity, The bed expands slightly at this condition, and the particles are free to move about (Fig. lb). As the velocity is increased further, bubbles can form. The soHds movement is more turbulent, and the bed expands to accommodate the volume of the bubbles. [Pg.69]

Fig. 1. Fluidized-bed behavior where U is the superficial gas velocity and is the minimum fluidization velocity (a) packed bed, no flow (b) fluid bed,... Fig. 1. Fluidized-bed behavior where U is the superficial gas velocity and is the minimum fluidization velocity (a) packed bed, no flow (b) fluid bed,...
After the SO converter has stabilized, the 6—7% SO gas stream can be further diluted with dry air, I, to provide the SO reaction gas at a prescribed concentration, ca 4 vol % for LAB sulfonation and ca 2.5% for alcohol ethoxylate sulfation. The molten sulfur is accurately measured and controlled by mass flow meters. The organic feedstock is also accurately controlled by mass flow meters and a variable speed-driven gear pump. The high velocity SO reaction gas and organic feedstock are introduced into the top of the sulfonation reactor,, in cocurrent downward flow where the reaction product and gas are separated in a cyclone separator, K, then pumped to a cooler, L, and circulated back into a quench cooling reservoir at the base of the reactor, unique to Chemithon concentric reactor systems. The gas stream from the cyclone separator, M, is sent to an electrostatic precipitator (ESP), N, which removes entrained acidic organics, and then sent to the packed tower, H, where SO2 and any SO traces are adsorbed in a dilute NaOH solution and finally vented, O. Even a 99% conversion of SO2 to SO contributes ca 500 ppm SO2 to the effluent gas. [Pg.89]


See other pages where Packings velocity is mentioned: [Pg.151]    [Pg.152]    [Pg.152]    [Pg.152]    [Pg.226]    [Pg.227]    [Pg.229]    [Pg.230]    [Pg.318]    [Pg.318]    [Pg.324]    [Pg.341]    [Pg.318]    [Pg.151]    [Pg.152]    [Pg.152]    [Pg.152]    [Pg.226]    [Pg.227]    [Pg.229]    [Pg.230]    [Pg.318]    [Pg.318]    [Pg.324]    [Pg.341]    [Pg.318]    [Pg.44]    [Pg.561]    [Pg.561]    [Pg.615]    [Pg.116]    [Pg.647]    [Pg.34]    [Pg.39]    [Pg.39]    [Pg.206]    [Pg.303]    [Pg.362]    [Pg.402]    [Pg.406]    [Pg.72]    [Pg.73]    [Pg.75]    [Pg.15]    [Pg.101]    [Pg.146]    [Pg.327]    [Pg.87]    [Pg.270]   
See also in sourсe #XX -- [ Pg.373 ]




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