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Simple Distillation Column

Consider first the design of distillation systems comprising only simple columns. These simple columns employ ... [Pg.129]

Much work has been carried out to find methods for the synthesis of distillation sequences of simple columns that do not involve heat integration. However, heat integration may have a significant... [Pg.130]

TABLE 5.1 The Number of Possible Distillation Sequences Using Simple Columns... [Pg.131]

Distillation. There is a large inventory of boiling liquid, sometimes under pressure, in a distillation column, both in the base and held up in the column. If a sequence of columns is involved, then, as discussed in Chap. 5, the sequence can be chosen to minimize the inventory of hazardous material. If all materials are equally hazardous, then choosing the sequence that tends to minimize the flow rate of nonkey components also will tend to minimize the inventory. Use of the dividing-wall column shown in Fig. 5.17c will reduce considerably the inventory relative to two simple columns. Dividing-wall columns are inherently safer than conventional arrangements because they lower not only the inventory but also the number of items of equipment and hence lower the potential for leaks. [Pg.263]

Establish the heat integration potential of simple columns. Introduce heat recovery between reboilers, intermediate reboilers, condensers, intermediate condensers, and other process streams. Shift the distillation column pressures to allow integration, where possible, using the grand composite curve to assess the heat integration potential. [Pg.348]

As pointed out in Chap. 5, replacing simple columns by complex columns tends to reduce the vapor (and heat) load but requires more of the heat to be added or removed at extreme levels. This means that the introduction of complex columns in the design might prejudice heat integration opportunities. Thus the introduction of complex distillation arrangements needs to be considered simultaneously with the heat integration. This can be carried out manually with some trial and error or using an automated procedure such as that of Kakhu and Flower. ... [Pg.349]

Cyclohexene can be prepared on a large scale still more rapidly and efficiently by the distillation of cyclohexanol over silica geP or, better, activated alumina. Using a 25-mm. tube packed with 8- to 14-mesh activated alumina (Aluminum Company of America) and heated to 380-450 over a 30-cm. length, 1683 g. of cyclohexanol was dehydrated in about four hours. After separating the water, drying with sodium sulfate, and fractionating with a simple column, 1222 g. (89 per cent yield) of cyclohexene, b.p. 82-84 , was obtained. [Pg.27]

Consider the material balance for a simple binary distillation column. A simple column has one feed, two products, one reboiler and one condenser. Such a column is shown in Figure 9.5. An overall material balance can be written as ... [Pg.160]

Table 11.1 Number of possible distillation sequences using simple columns. Table 11.1 Number of possible distillation sequences using simple columns.
This remixing that occurs in both sequences of simple distillation columns is a source of inefficiency in the separation. By contrast, consider the prefractionator arrangement shown in Figure 11.9. In the prefractionator, a crude split is performed so that Component B is distributed between the top and bottom of the column. The upper section of the prefractionator separates AB from C, whilst the lower section separates BC from A. Thus, both sections remove only one component from the product of that column section and this is also true for all four sections of the main column. In this way, the remixing effects that are a feature of both simple column sequences are avoided4. [Pg.219]

The elimination of mixing losses in the prefractionator arrangement means that it is inherently more efficient than an arrangement using simple columns. The same basic arguments apply to both distributed distillation and prefractionator arrangements, with the additional degree of... [Pg.219]

Consider now ways in which the best arrangement of a distillation sequence can be determined more systematically. Given the possibilities for changing the sequence of simple columns or the introduction of prefractionators, side-strippers, side-rectifiers and fully thermally coupled arrangements, the problem is complex with many structural options. The problem can be addressed using the optimization of a superstructure. As discussed in Chapter 1, this approach starts by setting up a grand flowsheet in which all structural features for an optimal solution are embedded. [Pg.228]

Table 11.10 presents some heuristics for using complex distillation columns to separate a ternary mixture into its pure component products. On the basis of these heuristics and those for simple columns, suggest two sequences containing complex columns that can be used to separate the mixture described in Table 11.9 into relatively pure products. [Pg.231]

The results received form the optimization using inherent safety as the objective function are somewhat different compared to those calculated with an economic objective function earlier (Hurme, 1996). With the inherent safety objective function the simple distillations were favoured more than with the economic function. Exceptions are cases where the extractive distillation could improve separation very dramatically. This is because in simple distillations only one column is required per split, but in extractive distillation two columns are needed, since the solvent has to be separated too. This causes larger fluid inventory since also the extraction solvent is highly flammable. The results of the calculation are well justified by common sense, since one of the principles of inherent safety is to use simpler designs and reduce inventories to enhance safety. [Pg.115]

Unlike simple columns, these complex configurations produce more than two products and feature more than a single light and heavy key component. A task-based representation of these schemes is accomplished with the ideas of hybrids and sloppy splits. Additional tasks are made up of different simple tasks. They are subsequently termed hybrid tasks and are defined as an ordered combination of simple distillation tasks, as illustrated in Figure 9. [Pg.436]

For single separation duty, Bernot et al. (1991) presented a method to estimate batch sizes, operating times, utility loads, costs, etc. for multicomponent batch distillation. The approach is similar to that of Diwekar et al. (1989) in the sense that a simple short cut technique is used to avoid integration of a full column model. Their simple column model assumes negligible holdup and equimolal overflow. The authors design and, for a predefined reflux or reboil ratio, minimise the total annual cost to produce a number of product fractions of specified purity from a multicomponent mixture. [Pg.154]

When setting a column specification, some other variable must be allowed to change in order to meet the specification, and it and other variables should be particularly sensitive to the specification. For instance, in a complex column, the bottoms purity can be more sensitive o an interreboiler duly rather than that of the reboiler, especially if the interreboiler duty is large. In a simple column with a small condenser duty relative to the reboiler duty, the distillate purity will be more sensitive to reboiler duty. [Pg.193]

This subsection describes how to generate the feasible combinatorial possibilities of distillation column configurations for separation of mixtures that do not form azeotropes. Components are named A, B, C, D,. . . and they are listed in the order of decreasing volatility (or increasing boiling temperature). We limit our considerations to splits where the most volatile (lightest) component and the least volatile (heaviest) component do not distribute between the top and bottom product. For simplicity we consider only separations where final products are relatively pure components. Systems containing simultaneously simple and complex distillation columns are considered. Simple columns are the conventional columns with one feed stream and two product streams complex columns have multiple feeds and/or multiple product streams. [Pg.59]

Finally, the bottom product of the extractive distillation column, ED-4, can be separated in a simple column since it contains the nonazeotropic species methanol and water only. This column is shown is Fig. 39, again based on a rigorous simulation. [Pg.128]

It is convenient to have some standard by which to compare columns, and this is commonly referred to as the theoretical plate, which is simply the effect of one simple distillation. A column which will effect a separation equivalent to six simple distillations (taking only the first very small fraction in each case) is said to have six theoretical plates. [Pg.42]

The atmospheric distillation column in a refinery is highly complex system because of the interactions between the main column with different side strippers and draw streams where the study of this complex system will be more difficult. However, the decomposition of the complex column into a series of simple columns ease and simplify its study. There are a number of advantages of decomposing a complex tower, namely ... [Pg.170]

The available standard shortcut methods and distillation design procedures are not applicable to complex columns. However, they are for simple columns. For complex mixtures, e.g. crude oil, the standard shortcut methods are not accurate for designing the crude oil distillation column. However, these methods are used to get a starting estimation for designing the column. [Pg.171]


See other pages where Simple Distillation Column is mentioned: [Pg.129]    [Pg.348]    [Pg.24]    [Pg.159]    [Pg.211]    [Pg.219]    [Pg.628]    [Pg.49]    [Pg.96]    [Pg.1604]    [Pg.394]    [Pg.433]    [Pg.433]    [Pg.435]    [Pg.98]    [Pg.135]    [Pg.71]    [Pg.176]    [Pg.235]    [Pg.49]    [Pg.1505]    [Pg.1231]   


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