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Column operation

Fixed Bed Columns. Column contactors allow multiple equilibrium stages to be obtained in a single unit. This contactor provides for reactions to be driven to the desired level of completion in a single pass by adjusting the resin bed depth and the flow conditions. The main components of a column contactor are shown in Fig. 28. At the end of its useful work cycle, the resin is backwashed, regenerated and rinsed for subsequent repetition of the work cycle. Typically, diis nonproductive portion of the cycle is a small fraction of the total operating cycle. [Pg.446]

Column contactors may be operated in cocurrent, countercurrent or fluidized bed modes of operation. The cocurrent mode means that the regenerant solution flows through the column in the same direction as the feed solution. The countercurrent mode has the regenerant flowing in the opposite direction as the feed solution. [Pg.446]

Countercurrent operation of a column may be preferred to reduce the ion leakage from a column. Ion leakage is defined as the amount of ion being [Pg.446]

The fixed bed column is essentially a simple pressure vessel. Each vessel requires a complexity of ancillary equipment. Each column in a cascade will require several automatic control valves and associated equipment involving process computer controls to sequence the proper flow of different influent streams to the resin bed. [Pg.447]

Service Backwash Simultaneous Mixing Cycle Regeneration [Pg.448]


Figure 3.8a shows the temperature-composition diagram for a minimum-boiling azeotrope that is sensitive to changes in pressure. This azeotrope can be separated using two columns operating at different pressures, as shown in Fig. 3.86. Feed with mole fraction of A Ufa)) of, say, 0.3 is fed to the high-pressure column. The bottom product from this high-pressure column is relatively pure B, whereas the overhead is an azeotrope with jcda = 0-8, jcdb = 0.2. This azeotrope is fed to the low-pressure column, which produces relatively pure A in the bottom and in the overhead an azeotrope with jcda = 0.6, jcdb = 0.4. This azeotrope is added to the feed of the high-pressure column. Figure 3.8a shows the temperature-composition diagram for a minimum-boiling azeotrope that is sensitive to changes in pressure. This azeotrope can be separated using two columns operating at different pressures, as shown in Fig. 3.86. Feed with mole fraction of A Ufa)) of, say, 0.3 is fed to the high-pressure column. The bottom product from this high-pressure column is relatively pure B, whereas the overhead is an azeotrope with jcda = 0-8, jcdb = 0.2. This azeotrope is fed to the low-pressure column, which produces relatively pure A in the bottom and in the overhead an azeotrope with jcda = 0.6, jcdb = 0.4. This azeotrope is added to the feed of the high-pressure column.
Distillation capital costs. The classic optimization in distillation is to tradeoff capital cost of the column against energy cost for the distillation, as shown in Fig. 3.7. This wpuld be carried out with distillation columns operating on utilities and not integrated with the rest of the process. Typically, the optimal ratio of actual to minimum reflux ratio lies in the range 1.05 to 1.1. Practical considerations often prevent a ratio of less than 1.1 being used, as discussed in Chap. 3. [Pg.349]

The relative retention is dependent on (1) the nature of the stationary and mobile phases and (2) the column operating temperature. [Pg.1105]

It is possible to dispense with the extraction step if the oxidation section is operated at high propylene concentrations and low steam levels to give a concentrated absorber effluent. In this case, the solvent recovery column operates at total organic reflux to effect a2eotropic dehydration of the concentrated aqueous acryflc acid. This results in a reduction of aqueous waste at the cost of somewhat higher energy usage. [Pg.154]

The methanol carbonylation is performed ia the presence of a basic catalyst such as sodium methoxide and the product isolated by distillation. In one continuous commercial process (6) the methyl formate and dimethylamine react at 350 kPa (3.46 atm) and from 110 to 120°C to effect a conversion of about 90%. The reaction mixture is then fed to a reactor—stripper operating at about 275 kPa (2.7 atm), where the reaction is completed and DMF and methanol are separated from the lighter by-products. The cmde material is then purified ia a separate distillation column operating at atmospheric pressure. [Pg.513]

The dominance of distiHation-based methods for the separation of Hquid mixtures makes a number of points about RCM and DRD significant. Residue curves trace the Hquid-phase composition of a simple single-stage batch stiHpot as a function of time. Residue curves also approximate the Hquid composition profiles in continuous staged or packed distillation columns operating at infinite reflux and reboil ratios, and are also indicative of many aspects of the behavior of continuous columns operating at practical reflux ratios (12). [Pg.446]

Distillation columns are controlled by hand or automatically. The parameters that must be controlled are (/) the overall mass balance, (2) the overall enthalpy balance, and (J) the column operating pressure. Modem control systems are designed to control both the static and dynamic column and system variables. For an in-depth discussion, see References 101—104. [Pg.176]

In the chemical engineering domain, neural nets have been appHed to a variety of problems. Examples include diagnosis (66,67), process modeling (68,69), process control (70,71), and data interpretation (72,73). Industrial appHcation areas include distillation column operation (74), fluidized-bed combustion (75), petroleum refining (76), and composites manufacture (77). [Pg.540]

AOC provide the additional advantages of reducing ground-space requirements and piping and pumping requirements and of providing smoother column operation. [Pg.1081]

If a relatively sharp separation is required between two components of adjacent volatihty, but either an undesirably low temperature is required to produce reflux at the column-operating pressure or an undesirably high temperature is required to produce boil-up, then refluxed stripping as shown in Fig. I3-7g or reboiled absorption... [Pg.1244]

FIG. 13-37 McCabe-Thiele diagrams for limiting cases, a) Minimum stages for a column operating at total reflux with no feeds or products, (h) Minimum reflux for a binary system of normal volatility. [Pg.1271]

The (x, i )), values in Eq. (13-37) are minimum-reflux values, i.e., the overhead concentration that would be produced by the column operating at the minimum reflux with an infinite number of stages. When the light key and the heavy key are adjacent in relative volatihty and the specified spht between them is sharp or the relative volatilities of the other components are not close to those of the two keys, only the two keys will distribute at minimum reflux and the Xi D),n values are easily determined. This is often the case and is the only one considered here. Other cases in which some or all of the nonkey components distribute between distillate and bottom products are discussed in detail by Henley and Seader (op. cit.). [Pg.1274]

Regardless of the procedure used, certain initial steps must be taken for the determination or specification of certain product properties and yields based on the TBP distillation curve of the column feed, method of providing column reflux, column-operating pressure, type of condenser, and type of side-cut strippers ana stripping requirements. These steps are developed and ilhistrated with several detailed examples by Watkins (op. cit.). Only one example, modified from one given by Watkins, is considered briefly here to indicate the approach taken during the initial steps. [Pg.1328]

In operation, a batch of liquid is charged to the pot and the system is first brought to steady state under total reflux. A portion of the overhead condensate is then continuously withdrawn in accordance with the established reflux pohcy. Cuts are made by switching to alternate receivers, at which time operating conditions may be altered. The entire column operates as an enriching section. As time proceeds, composition of the material being distilled becomes less rich in the more volatile components, and distillation of a cut is stopped when accumulated distillate attains the desired average composition. [Pg.1334]

Other control methods. A cychng procedure can be used to set the pattern for column operation. The unit operates at total reflux until equilibrium is established. Distillate is then taken as total draw-... [Pg.1335]

Most plate columns operate under conditions such that gas is completely mixed as it flows between the plates, but few operate with pure plug flow of liquid. Departure from plug flow of liquid has been studied by Gautreaux and O Connell [Chem. Eng. Pi oq., 51, 232 (1955)] by assuming that hquid mixing can be represented as occurring in a series of stages of completely mixed liquid. For this model,... [Pg.1383]

Dislribttlors Most spray columns operate with the drops being formed at the ends of jets from the dispersed phase inlet distributor. The orifices or nozzles for introducing the dispersed phase are usually not smaller than 0.13 cm (0.05 in) in diameter in order to avoid clogging, nor larger than 0.64 cm (0.25 in) in order to avoid formation of... [Pg.1474]

Column Operation To assure intimate contact between the counterflowing interstitial streams, the volume fraction of liquid in the foam should be kept below about 10 percent—and the lower the better. Also, rather uniform bubble sizes are desirable. The foam bubbles will thus pack together as blunted polyhedra rather than as spheres, and the suction in the capillaries (Plateau borders) so formed vidll promote good liqiiid distribution and contact. To allow for this desirable deviation from sphericity, S = 6.3/d in the equations for enriching, stripping, and combined column operation [Lemhch, Chem. E/ig., 75(27), 95 (1968) 76(6), 5 (1969)]. Diameter d still refers to the sphere. [Pg.2020]

Determination of pressure drop through the column (for packed columns, correlations dependent of packing type, column-operating data, and physical properties of the constituents involved are available to estimate the pressure drop through the packing for plate columns, the pressure drop per plate is obtained and multiplied by the number of plates)... [Pg.2185]


See other pages where Column operation is mentioned: [Pg.1109]    [Pg.67]    [Pg.378]    [Pg.483]    [Pg.496]    [Pg.294]    [Pg.336]    [Pg.337]    [Pg.108]    [Pg.333]    [Pg.336]    [Pg.511]    [Pg.172]    [Pg.181]    [Pg.181]    [Pg.190]    [Pg.1243]    [Pg.1270]    [Pg.1292]    [Pg.1296]    [Pg.1302]    [Pg.1308]    [Pg.1310]    [Pg.1311]    [Pg.1334]    [Pg.1394]    [Pg.1545]    [Pg.1988]    [Pg.1994]    [Pg.2115]    [Pg.2144]   
See also in sourсe #XX -- [ Pg.167 , Pg.173 ]




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