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5.2. Distillation columns and their process calculations 
There are many types of distillation columns each of which is designed to perform specific types of separations. One way of classifying distillation column type is to look at how they are operated. Based on operation, they are of two types: batch or differential and continuous columns.

5.2.1. Batch or differential distillation columns and their process calculation 
In batch operation, the feed is introduced batch-wise to the column. That is, the column is charged with a 'batch' and then the distillation process is carried out. When the desired task is achieved, a next batch of feed is introduced. Consider a binary mixture of components A (more volatile) and B (less volatile). The system consists of a batch of liquid (fixed quantity) inside a kettle (or still) fitted with heating element and a condenser to condense the vapor produced as shown in Figure 5.7. The condensed vapor is known as the distillate. The distillate is collected in a condensate receiver. The liquid remaining in the still is known as the residual. The process is unsteady state. The concentration changes can be analyzed using the phase diagram, and detailed mathematical calculations carried out using the Rayleigh Equation. Readers are suggested to follow chapter 9 (Page 369) of text book “Mass-transfer operations” by R. E Treybal, third edition. As the process is unsteady state, the derivation is based on a differential approach to changes in concentration with time. Let L1 = initial moles of liquid originally in still, L2 = final moles of liquid remained in still, x1 = initial liquid composition in still (mole fraction of A), x2 = final liquid composition in still (mole fraction A). At any time t, the amount of liquid in the still is L, with mole fraction of A in the liquid being x. After a small differential time (t + dt), a small amount of vapor dL is produced, and the composition of A in the vapor is y (mole fraction). The vapor is assumed to be in equilibrium with the residue liquid. The amount of liquid in the still is thus reduced from L to (L - dL), while the liquid composition changed from x to (x - dx). Then the material balance on A can be written as:
Distillation Columns And Their Process Calculations | Mass Transfer - Chemical Engineering
Figure 5.7: Simple batch or differential distillation process

Initial amount in still = Amount left in still + Amount vaporized
Distillation Columns And Their Process Calculations | Mass Transfer - Chemical Engineering                                      (5.6) 
or
Distillation Columns And Their Process Calculations | Mass Transfer - Chemical Engineering                             (5.7)
Neglecting the term (dx)(dL), the Equation (5.7) may be written as:
Distillation Columns And Their Process Calculations | Mass Transfer - Chemical Engineering                  (5.8)
Re-arranging and Integrating from L1 to L2, and from x1 to x2, one can obtain the following Equation which is called Rayleigh Equation:
Distillation Columns And Their Process Calculations | Mass Transfer - Chemical Engineering         (5.9)
The integration of Equation (5.9) can be obtained graphically from the equilibrium curve, by plotting 1/(y-x) versus x.

Example problem 5.1 
A mixture of 40 mole % isopropanol in water is to be batch-distilled at 1 atm until 70 mole % of the charge has been vaporized. Calculate the composition of the liquid residue remaining in the still pot, and the average composition of the collected distillate. VLE data for this system, in mole fraction of isopropanol, at 1 atm are :
Distillation Columns And Their Process Calculations | Mass Transfer - Chemical Engineering

Solution 5.1: 
Calculate 1/(y-x)
As per Rayleigh Equation 
Distillation Columns And Their Process Calculations | Mass Transfer - Chemical Engineering
x1= 0.4
Feed L1 = 100
Distillate (D) = 70
Liquid residue as L2 = L1-D = 30
Find xby equating Distillation Columns And Their Process Calculations | Mass Transfer - Chemical Engineering 
The value of x2 = 0.067
Distillation Columns And Their Process Calculations | Mass Transfer - Chemical Engineering

The document Distillation Columns And Their Process Calculations | Mass Transfer - Chemical Engineering is a part of the Chemical Engineering Course Mass Transfer.
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FAQs on Distillation Columns And Their Process Calculations - Mass Transfer - Chemical Engineering

1. What is the purpose of a distillation column in chemical engineering?
Ans. A distillation column is used in chemical engineering to separate a mixture of two or more liquids with different boiling points. It works on the principle of vapor-liquid equilibrium, where the more volatile component vaporizes and rises up the column while the less volatile component remains in the liquid phase and flows down the column.
2. How does a distillation column work?
Ans. A distillation column works by utilizing the difference in boiling points of the components in a liquid mixture. The mixture is fed into the column, and heat is applied at the bottom. As the liquid heats up, the more volatile component vaporizes and rises up the column, while the less volatile component remains in the liquid phase and flows down. The rising vapor encounters a series of trays or packing material in the column, which provides a large surface area for contact between the vapor and liquid phases. This allows for mass transfer and separation of the components. The separated components are then collected at different points along the column.
3. What are the key calculations involved in designing a distillation column?
Ans. The key calculations involved in designing a distillation column include determining the number of theoretical stages or trays required for separation, estimating the column diameter, and calculating heat duty requirements. The number of stages can be determined using various methods such as the McCabe-Thiele method or the Fenske-Underwood-Gilliland method. The column diameter can be estimated based on factors such as vapor and liquid flow rates, pressure drop considerations, and desired separation efficiency. Heat duty calculations involve determining the amount of heat required to vaporize the feed and any additional heat needed for temperature control within the column.
4. How can the efficiency of a distillation column be improved?
Ans. The efficiency of a distillation column can be improved by optimizing various parameters such as reflux ratio, feed location, and tray or packing design. The reflux ratio is the ratio of the liquid returned to the column to the liquid withdrawn as product. Increasing the reflux ratio can improve separation efficiency but also requires more energy. The location of the feed entry point can also impact efficiency, with optimal placement depending on factors such as relative volatility of the components and desired separation. Additionally, choosing the appropriate tray or packing design can enhance mass transfer and separation efficiency.
5. What are the main challenges in distillation column operation?
Ans. The main challenges in distillation column operation include maintaining proper temperature and pressure control, managing fouling or scaling on trays or packing, and dealing with non-ideal behavior of the components. Temperature and pressure control are crucial for achieving desired separation and preventing any operational issues. Fouling or scaling can occur due to impurities in the feed or reaction products, reducing column efficiency and requiring maintenance. Non-ideal behavior, such as azeotropes or high boiling point elevations, can pose challenges in achieving complete separation and may require additional techniques such as solvent addition or multiple columns.
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