Distillation column design extractive

Whereas there is extensive Hterature on design methods for azeotropic and extractive distillation, much less has been pubUshed on operabiUty and control. It is, however, widely recognized that azeotropic distillation columns are difficult to operate and control because these columns exhibit complex dynamic behavior and parametric sensitivity (2—11). In contrast, extractive distillations do not exhibit such complex behavior and even highly optimized columns are no more difficult to control than ordinary distillation columns producing high purity products (12). 

Extractive Distillation Design and Optimization Extractive distillation column composition profiles have a veiy characteristic... 

This chapter concerns the most important reactive separation processes reactive absorption, reactive distillation, and reactive extraction. These operations combining the separation and reaction steps inside a single column are advantageous as compared to traditional unit operations. The three considered processes are similar and at the same time very different. Therefore, their common modeling basis is discussed and their peculiarities are illustrated with a number of industrially relevant case studies. The theoretical description is supported by the results of laboratory-, pilot-, and industrial-scale experimental investigations. Both steady-state and dynamic issues are treated in addition, the design of column internals is addressed. 

The digital simulation of an extractive distillation column was performed in order to understand the dynamic behaviour of the system. Based on this results a considerably simplified dynamic model of sufficient accuracy could be developed. This model was employed in the design of a state observer and of an optimal control. After implementation in the large scale plant this new control system has proved to be highly efficient and reliable. 

The design of azeotropic or extractive distillation columns, as with con-A ventional columns, demands a knowledge of the vapor-liquid equilibrium properties of the system to be distilled. Such knowledge is obtained experimentally or calculated from other properties of the components of the system. Since the systems in azeotropic or extractive distillation processes have at least three components, direct measurement of the equilibrium properties is laborious and, therefore, expensive, so methods of calculation of these data are desirable. 

In 1992, a rather unusual furfural plant was built. With a front end according to the AGRIFURANE process described in chapter 10.2, the back end was designed as shown in Figure 112. The filtered reactor condensate containing 5 % furfural, 1.7 % acetic acid, 0.17 % formic acid, and various low boilers was introduced into an extraction tower 1 fed with chloroform at the top. On the way downwards, the heavy chloroform (density 1.498 g/cc at room temperature) picked up the furfural, and in view of the poor solubility of chloroform in water, it formed a chloroform/furfural extract at the bottom. This extract entered a distillation column 2 removing the chloroform as the head fraction. From a buffer tank 3, this chloroform was recycled to the extraction tower 1. The sump fraction of the distillation column 2 consisted of furfural, polymers, waxes, and some low boilers. This fraction was introduced into a distillation column 4, which yielded a head fraction of low boilers, a side stream of furfural, and a sump fraction of polymers and waxes. 

Solvent-based separation through extractive distillation consists of two distillations. The first is an extraction column with two feed (Aspen Distill was used designing this column), while the second is a simple distillation column (the driving force concept was used for designing this column). The design was then verified by rigorous simulation using Aspen Plus . The residue curve map (see Fig. 3) was used... 

Table 2 Input data and results from Aspen Distill for extraction column design...

Two different approaches have evolved for the simulation and design of multicomponent distillation columns. The conventional approach is through the use of an equilibrium stage model together with methods for estimating the tray efficiency. This approach is discussed in Chapter 13. An alternative approach based on direct use of matrix models of multicomponent mass transfer is developed in Chapter 14. This nonequilibrium stage model is also applicable, with only minor modification, to gas absorption and liquid-liquid extraction and to operations in trayed or packed columns. 

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