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Packed columns column packings

Packed Columns A packed column is constructed from glass, stainless steel, copper or aluminum and is typically 2-6 m in length, with an internal diameter of 2-4 mm. The column is filled with a particulate solid support, with particle diameters ranging from 37-44 pm to 250-354 pm. [Pg.564]

Figure 4. Breakthrough curves of Pb(II) in the adsorption of Pb(II) by FPS-f and FP-f packed columns. Column 1.5 ml of wet fiber (0.4 g in dry state), feeding solution 0.01 M lead nitrate. Flow rates in space velocity (h-1) are denoted on the figure. Figure 4. Breakthrough curves of Pb(II) in the adsorption of Pb(II) by FPS-f and FP-f packed columns. Column 1.5 ml of wet fiber (0.4 g in dry state), feeding solution 0.01 M lead nitrate. Flow rates in space velocity (h-1) are denoted on the figure.
Figure 6.2 Types of mass transfer equipment (a) packed column, (b) packings, (c) bubble column, and (d) packed bed. Figure 6.2 Types of mass transfer equipment (a) packed column, (b) packings, (c) bubble column, and (d) packed bed.
Gas chromatography was originally a technique for nonpolar analytes, and for such analytes nonpolar packed columns prevailed. Packed columns are typically a glass or stainless steel coil, 1-5 m total length and 2-5 mm internal diameter, which is filled with the stationary phase, or a packing coated with the stationary phase. Early packed columns had low plate numbers and in the majority of instances separation could not be obtained on the basis of the differences in volatility alone. The solution was selective stationary phases, and in the 1960s there were more than 200 different stationary phases available (41). [Pg.672]

Weight of Fish/Volume of Packing Material Column Packing (kg/m )... [Pg.117]

Chromatography is a separation process which depends on the differential distributions of the components of a mixture between a mobile bulk phase and an essentially thin film stationary phase.53-56 The stationary phase may be either in the form of a packed column (column chromatography) through which a mobile phase is allowed to flow, or in the form of a thin layer adhering to a suitable form of backing material (thin-layer chromatography) over which the mobile phase is allowed to ascend by capillary action. [Pg.197]

Fused silica capillary columns give better separation than packed columns. Columns having inside diameters of 0.25, 0.32, and 0.53 mm and film thickness between 0.25 and 1 pm have found use in herbicides analysis. The stationary phase is generally made out of phenyl silicone, methyl silicone, and cyanopropyl phenyl silicone in varying compositions. Some common columns are DB-5, DB-1701, DB-608, SPB-5, SPB-608, SPB-1701, Rtx-5, AT-1701, HP-608, BP-608, or equivalent. Use helium as carrier gas flow rate 30 cm/s on narrowbore columns with 0.25 or 0.32 mm ID and 7 mL/min for megabore 0.53 ID columns. [Pg.159]

In this procedure a Waters Associates liquid chromatograph was connected to anion exchange columns. Column packings used were p-Bondapak-NH2 and Nagel SA. The outlet of the liquid chromatograph was connected to the crossflow nebuliser of the ICP spectrometer (Jarrell-Ash-Atom-Comp 750) with Teflon tubing (0.15 x 13cm). Eluant flow rate was set at 1ml min 1... [Pg.156]

The measurement of column performance criteria to compare columns, column packings, and column loading procedures has long suffered from the non-standardization of test procedures and disagreement as to which of the many performance criteria are most significant. It is the purpose of this paper to point out several practical aspects which must be considered when designing experiments to test column performance. [Pg.31]

Figure 1.5c illustrates the variation of the resolution with the plate number N. The square root function initially rises steeply from a value of zero at N= 0. The rate of increase in Vn becomes quickly less with increasing N. At N= 2500 Yn equals 50. A value of 100 is reached for JV= 10,000, and 200 for IV=40,000. These three values of N may be seen as typical for three different kinds of chromatography packed column GC, packed column LC and capillary column GC. Within the constraints of any of these techniques, another factor of 2 in resolution by increasing N by a factor of 4 will be hard to achieve. [Pg.12]

Complex columns. Interreboilers, intercondensers, cooling coils, and side drawoffs are more easily incorporated in tray than in packed columns. In packed columns, every complexity requires additional distribution and/or liquid collection equipment. [Pg.520]

Air stripping is achieved by pumping groundwater to a packed column. The packing materials are used to provide large void volumes and a high surface area. The water flows downwards under gravity countercurrent to a stream of air. The... [Pg.41]

Various commercially-packed columns and packing materials are available and have been used for the separation and analysis of mixtures of sulphur gases (Bremner and Banwart, 1974 De Souza et al., 1975 Supelco, 1977). The most commonly-used columnpacking materials for sulphur-gas analysis are Chromosil 310, acetone-washed Porapak-QS and three types of Carbopak B. Selection must be based on the analytical data desired. Each of these packings separates different components and has advantages and disadvantages. [Pg.260]

Chromatographic columns vary in length from less than 2 m to 50 m or more. They are constructed of stainless steel, glass, fused silica, or Teflon. To fit into an oven for thermostating, they are usually formed into coils having diameters of 10 to 30 cm (Figure 31-6). A detailed discussion of columns, column packings, and stationary phases is found in Section 31B. [Pg.950]

As noted above, a number of equipment parameters must normally be specified so that the mass transfer coefficients can be estimated correctly. For example, the diameter of all columns must be known. For trayed columns, the tray type, weir height, liquid flow path length, and bubbling area must be known for packed columns, the packing type, size, and material must be known. It may also be necessary to allow for different diameters, tray or packing type, or other tray or packing parameters in different parts of the same column. [Pg.403]

For the purposes of simulating a packed column the packing was divided into a number of sections each of which is modeled as a nonequilibrium stage as discussed above. The C4 splitter was modeled using 150 nonequilibrium sections, an equilibrium reboiler and a total condenser. The bottom product rate in molar units and the reflux ratio were fixed at the values observed in the plant tests. Additional specifications included the component feed flows and the column pressures. [Pg.431]

Apply the concentrated solution to the head of a packed chromatographic column (packed with silica gel) using a Pasteur pipette. [Pg.112]

Guiochon, G., Conventional packed columns vs. packed or open mbular microcolumns in liquid chromatography. Arud. Chem. 1981, 53(9), 1318-1325. [Pg.299]

Chromatographic performance in terms of speed of analysis and resolving power has been found to be poor relative to conventional small particle packed columns. Although packed capillary columns have larger capacities their permeability is reduced. [Pg.358]

Packed columns column chromatography where the stationary phase is in the form of uniform particles which are packed into a column, the particles may be a solid material, e.g. silica gel or alumina or particles coated with a liquid stationary phase. [Pg.536]


See other pages where Packed columns column packings is mentioned: [Pg.170]    [Pg.2185]    [Pg.76]    [Pg.210]    [Pg.71]    [Pg.118]    [Pg.201]    [Pg.208]    [Pg.39]    [Pg.42]    [Pg.1941]    [Pg.777]    [Pg.113]    [Pg.470]    [Pg.75]    [Pg.2435]    [Pg.1371]    [Pg.78]    [Pg.129]    [Pg.731]    [Pg.118]    [Pg.421]    [Pg.2416]    [Pg.562]    [Pg.83]    [Pg.792]    [Pg.48]   
See also in sourсe #XX -- [ Pg.270 , Pg.580 ]




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