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5.2.2. Continuous distillation columns 
In contrast, continuous columns process a continuous feed stream. No interruptions occur unless there is a problem with the column or surrounding process units. They are capable of handling high throughputs. Continuous column is the more common of the two types.

Types of Continuous Columns 
Continuous columns can be further classified according to the nature of the feed that they are processing:
Binary distillation column: feed contains only two components
Multi-component distillation column: feed contains more than two components the number of product streams they have
Multi-product distillation column: column has more than two product streams where the extra feed exits when it is used to help with the separation,
Extractive distillation: where the extra feed appears in the bottom product stream
Azeotropic distillation: where the extra feed appears at the top product stream the type of column internals.
Tray distillation column: where trays of various designs are used to hold up the liquid to provide better contact between vapor and liquid, hence better separation. The details of the tray column are given in Module 4.
Packed distillation column: where instead of trays, 'packings' are used to enhance contact between vapor and liquid. The details of the packed column are given in Module

4.2.2.1. A single-stage continuous distillation (Flash distillation): 
A single-stage continuous operation occurs where a liquid mixture is partially vaporized. The vapor produced and the residual liquids are in equilibrium in the process are separated and removed as shown in Figure 5.8. Consider a binary mixture of A (more volatile component) and B (less volatile component). The feed is preheated before entering the separator. As such, part of the feed may be vaporized. The heated mixture then flows through a pressure-reducing valve to the separator. In the separator, separation between the vapor and liquid takes place. The amount of vaporization affects the concentration (distribution) of A in vapor phase and liquid phase. The relationship between the scale of vaporization and mole fraction of A in vapor and liquid (y and x) is known as the Operating Line Equation. Define f as molal fraction of the feed that is vaporized and withdrawn continuously as vapor. Therefore, for 1 mole of binary feed mixture, (1- f) is the molal fraction of the feed that leaves continuously as liquid. Assume, yD = mole fraction of A in vapor leaving, xB = mole fraction of A in liquid leaving, xF = mole fraction of A in feed entering. Based on the definition for f, the greater the heating is, the larger the value of f. If the feed is completely vaporized, then f = 1.0 Thus, the value of f can varies from 0 (no vaporization) to 1 (total vaporization). From material balance for the more volatile component (A) one can write
Continuous Distillation Columns | Mass Transfer - Chemical Engineering                              (5.10)

Or,

Continuous Distillation Columns | Mass Transfer - Chemical Engineering                               (5.11)


Continuous Distillation Columns | Mass Transfer - Chemical Engineering
Figure 5.8: Flash distillation process

The Equation (5.11) on rearranging becomes:
Continuous Distillation Columns | Mass Transfer - Chemical Engineering                                                                  (5.12)

The fraction f depends on the enthalpy of the liquid feed, the enthalpies of the vapor and liquid leaving the separator. For a given feed condition, and hence the known value of f and xF, the Equation (5.12) is a straight line Equation with slope - (1-f)/f and intercept xF/f as shown in Figure 5.9. It will intersect the equilibrium line at the point (xB, yD). From this value, the composition of the vapor and liquid leaving the separator can be obtained. 
Continuous Distillation Columns | Mass Transfer - Chemical Engineering
Figure 5.9: Graphical presentation of flash veporization

5.2.2.2. Multi-stage Continuous distillation-Binary system 
A general schematic diagram of a multistage counter-current binary distillation operation is shown in Figure 4.10. The operation consists of a column containing the equivalent N number of theoretical stages arranged in a two-section cascade; a condenser in which the overhead vapor leaving the top stage is condensed to give a liquid distillate product and liquid reflux that is returned to the top stage; a reboiler in which liquid from the bottom stage is vaporized to give a liquid bottom products and the vapor boil off returned to the bottom stage; accumulator is a horizontal (usually) pressure vessel whereby the condensed vapor is collected; Heat exchanger where the hot bottoms stream is used to heat up the feed stream before it enters the distillation column. The feed enters the column at feed stage contains more volatile components (called light key, LK) and less volatile components (called heavy key, HK). At the feed stage feed may be liquid, vapor or mixture of liquid and vapor. The section above the feed where vapor is washed with the reflux to remove or absorb the heavy key is called enriching or rectifying section. The section below the feed stage where liquid is stripped of the light key by the rising vapor is called stripping section.
Continuous Distillation Columns | Mass Transfer - Chemical Engineering

Figure 5.10: Multi-stage binary distillation column

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FAQs on Continuous Distillation Columns - Mass Transfer - Chemical Engineering

1. What is a continuous distillation column?
Ans. A continuous distillation column is a chemical engineering equipment used for separating liquid mixtures into their individual components based on their boiling points. It operates in a continuous manner, allowing the feed mixture to enter at one end and the separated components to exit at different points along the column.
2. How does a continuous distillation column work?
Ans. A continuous distillation column works on the principle of fractional distillation. The feed mixture is heated and introduced at the bottom of the column. As the mixture rises through the column, it encounters trays or packing material that provide a large surface area for contact between the rising vapor and descending liquid. The components with lower boiling points vaporize more easily and tend to concentrate in the rising vapor, whereas the components with higher boiling points remain in the liquid phase.
3. What factors affect the performance of a continuous distillation column?
Ans. Several factors can affect the performance of a continuous distillation column. These include the composition and temperature of the feed mixture, the number of trays or packing material in the column, the reflux ratio (ratio of condensed liquid returning to the column), and the pressure inside the column. Additionally, the efficiency of the column can be influenced by any heat loss or non-idealities in the separation process.
4. What are the advantages of using a continuous distillation column?
Ans. Continuous distillation columns offer several advantages in chemical engineering processes. They provide a continuous and efficient method for separating mixtures, allowing for large-scale production. They can handle a wide range of feed compositions and provide high purity separation. Additionally, continuous distillation columns can be operated at different pressures to optimize the separation process and are easily scalable for different production capacities.
5. What are some common applications of continuous distillation columns?
Ans. Continuous distillation columns find applications in various industries, including petroleum refining, petrochemical production, pharmaceutical manufacturing, and alcohol distillation. They are used to separate crude oil into different fractions, produce pure solvents or chemicals from mixtures, and purify pharmaceutical compounds. Additionally, continuous distillation columns are employed in the production of ethanol and other alcoholic beverages.
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