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MORE COMPLEX DISTILLATION SYSTEMS

In the example distillation system considered in Chapters 3 and 4, we studied the binary propane/isobutane separation in a single distillation column. This is a fairly ideal system from the standpoint of vapor-liquid equilibrium (VLE), and it has only two components, a single feed and two product streams. In this chapter, we will show that the steady-state simulation methods can be extended to multicomponent nonideal systems and to more complex column configurations. [Pg.95]


In this section we present more complex distillation column processes that go beyond the plain vanilla variety. Industry uses columns with multiple feeds, sidestreams, combinations of columns, and heat integration to improve the efficiency of the separation process. Very significant reductions in energy consumption are possible with these more complex configurations. However, they also present more challenging control problems. We briefly discuss some common control structures for these systems. [Pg.218]

An alternative to the constant-reflux-ratio policy described above is to maintain a constant-molar-vapor rate, but continuously vary the reflux ratio to achieve a constant distillate composition that meets the specified purity. This policy requires a more complex control system, which may be justified only for large batch distillation systems. [Pg.402]

It is hoped that from this chapter the reader understands the context and importance of industrial distillation, and realizes why efficient and insightful design techniques are so important. Although it is a comparatively old separation technique, there is still much room for improvement, especially in the area of complex distillation. The CPM technique that is presented in this book will aid in understating simple and complex distillation systems more clearly. Although the premise of the CPM technique is reasonably easy to follow and comprehend, it is a rather advanced technique, not recommended as a reader s first introduction to the field of distillation. [Pg.12]

This chapter introduces how continuous distillation columns work and serves as the lead to a series of nine chapters on distillation. The basic calculation procedures for binary distillation are developed in Chapter 4. Multicomponent distillation is introduced in Chapter 5. detailed conputer calculation procedures for these systems are developed in Chapter 6. and sinplified shortcut methods are covered in Chapter 7. More complex distillation operations such as extractive and azeotropic distillation are the subject of Chapter 8. Chapter 9 switches to batch distillation, which is commonly used for smaller systems. Detailed design procedures for both staged and packed columns are discussed in Chapter 10. Finally, Chapter 11 looks at the economics of distillation and methods to save energy (and money) in distillation systems. [Pg.122]

The choice of separation method to be appHed to a particular system depends largely on the phase relations that can be developed by using various separative agents. Adsorption is usually considered to be a more complex operation than is the use of selective solvents in Hquid—Hquid extraction (see Extraction, liquid-liquid), extractive distillation, or azeotropic distillation (see Distillation, azeotropic and extractive). Consequentiy, adsorption is employed when it achieves higher selectivities than those obtained with solvents. [Pg.291]

In order to determine the packed height it is necessary to obtain a value of the overall number of transfer units methods for doing this are available for binary systems in any standard text covering distillation (73) and, in a more complex way, for multicomponent systems (81). However, it is simpler to calculate the number of required theoretical stages and make the conversion ... [Pg.173]

The mechanism by which nonkey components affect a given separation is more complex in practice than the broad arguments presented here. There are complex interrelationships between the volatility of the key and nonkey components, and so on. Also, it is often the case that the distillations system has constraints to prevent certain heat integration opportunities. Such constraints will often present themselves as constraints over which the pressure of the distillation columns will operate. For example, it is often the case that the maximum pressure of a distillation column is restricted to avoid decomposition of material in the reboiler. This is especially the case when reboiling high molar mass material. Distillation of high molar mass material is often constrained to operate under vacuum conditions. Clearly, if the pressure of the distillation column is constrained, then this restricts the heat integration opportunities. Another factor that can create... [Pg.452]

If it were possible to identify or quantitatively determine any element or compound by simple measurement no matter what its concentration or the complexity of the matrix, separation techniques would be of no value to the analytical chemist. Most procedures fall short of this ideal because of interference with the required measurement by other constituents of the sample. Many techniques for separating and concentrating the species of interest have thus been devised. Such techniques are aimed at exploiting differences in physico-chemical properties between the various components of a mixture. Volatility, solubility, charge, molecular size, shape and polarity are the most useful in this respect. A change of phase, as occurs during distillation, or the formation of a new phase, as in precipitation, can provide a simple means of isolating a desired component. Usually, however, more complex separation procedures are required for multi-component samples. Most depend on the selective transfer of materials between two immiscible phases. The most widely used techniques and the phase systems associated with them are summarized in Table 4.1. [Pg.48]

To illustrate the concept, consider a single distillation column with distillate and bottoms products. To produce these products while using the minimum amount of energy, the compositions of both products should be controlled at their specifications. Figure 8.13u shows a dual composition control system. The disadvantages of this structure arc (1) two composition analyzers are required, (2) the instrumentation is more complex, and (3) there may be dynamic interaction problems since the two loops are interacting. This system may be difficult to design and to tune. [Pg.275]

Example 12.6. Let us consider a much more complex system where the advantages of frequencynlomain solution will be apparent. Rippin and Lamb showed how a frequency-domain stepping technique could be used to find the frequency response of a binary, equimolal-overflow distillation column. The column has many trays and therefore the system is of very high order. [Pg.444]

The comparison between the two major seawater desalting alternatives, reverse osmosis and distillation, is more complex then ever. The location, system size, time of implementation and economic parameters, especially the price of conventional energy and also the possibility of use of non-conventional energy in the future, such as solar or geothermal energy sources, may greatly affect the final decision. [Pg.71]

A simple distillation tower, like that shown in Fig. 3.2, also must obey its own phase rule. Here, because the distillation tower is a more complex system than the reflux drum, there are three independent... [Pg.32]

An ideal mixture of n components requires a sequence of n - 1 conventional distillation columns (two product streams) to separate the components completely. The columns can be arranged sequentially without recycle between them. This picture changes when mixtures forming azeotropes must be separated. Nonideal systems sometimes require complex distillation arrangements involving more than n - 1 columns with recycle of material between the columns. For the analysis of such systems, we recommend the use of residue curve maps. We base the following summary on the excellent book by Doherty and Malone (1998), who pioneered the use of these techniques. [Pg.187]

However we choose to look at it, a basic distillation column has two control degrees of freedom. When we turn to more complex column configurations with sidestreams, side strippers, side rectifiers, intermediate reboilers and condensers, and the like, we add additional control degrees of freedom. These more complex systems are discussed in Sec. 6.8. [Pg.198]


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