/*! This file is auto-generated */ .wp-block-button__link{color:#fff;background-color:#32373c;border-radius:9999px;box-shadow:none;text-decoration:none;padding:calc(.667em + 2px) calc(1.333em + 2px);font-size:1.125em}.wp-block-file__button{background:#32373c;color:#fff;text-decoration:none} Problem 16 A distillation column having eig... [FREE SOLUTION] | 91Ó°ÊÓ

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A distillation column having eight theoretical stages (seven in the column + partial reboiler + total condenser) is being used to separate 100 krnollh of a saturated-liquid feed containing 50 mol% A into a product stream containing 90 mol% A. The liquid-to-vapor molar ratio at the top plate is 0.75. The saturated-liquid feed is introduced on plate 5 from the top. Determine: (a) The composition of the bottoms, (b) The L/V ratio in the stripping section, and (c) The moles of bottoms per hour. Unbeknown to the operators, the bolts holding plates 5, 6, and 7 rust through, and the plates fall into the still pot. If no adjustments are made, what is the new bottoms composition? It is suggested that, instead of returning reflux to the top plate, an equivalent amount of liquid product from another column be used as reflux. If this product contains 80 mol% A, what now is the composition of: (a) The distillate, and (b) The bottoms. EQUILIBRIUM DATA, MOLE FRACTION OF A y 0.19 0.37 0.5 0.62 0.71 0.78 0.84 0.9 0.96 x 0.1 0.2 0.3 0.4 0.5 0.6 0.7 0.8 0.9

Short Answer

Expert verified
The original bottom composition (x_B) is solved using McCabe-Thiele. Failure leads to lower purity. Using 80% A as reflux changes distillate (now less pure) and bottom compositions, recalculated as specified.

Step by step solution

01

Understanding the Problem

The problem involves a distillation column with eight theoretical stages and asks for (a) the composition of the bottoms, (b) the L/V ratio in the stripping section, and (c) the moles of bottoms per hour. We also need to find new compositions after plates 5, 6, and 7 fall, and when an 80 mol% A liquid is used as reflux.
02

McCabe-Thiele Method for Distillation Columns

Use the McCabe-Thiele method to understand the column performance. The given equilibrium data helps in constructing the equilibrium curve for separation. The number of stages, feed condition, reflux condition, and product compositions guide the operating lines.
03

Construct Equilibrium Curve

Plot the equilibrium curve using the provided data: y = [0.19, 0.37, 0.5, 0.62, 0.71, 0.78, 0.84, 0.9, 0.96] versus x = [0.1, 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9]. This graph visually represents the separation potential for this distillation setup.
04

Calculate Operating Lines

To find the operating lines, use the reflux ratio ( R = 0.75 ) and top product purity (90 mol% A). The rectifying line connects this point with the top corner (0,0) of the diagram. Calculate the bottom line using the material balance and the new position of the bottom stage after the plates fall.
05

Material and Energy Balances

Perform a mass balance over the column: Feed is 50 mol% A, Distillate is 90 mol% A. Overall: F = D + B and the component balance: Fz_F = Dx_D + Bx_B . Pre-failure, the reboiler and condenser assist define x_B.
06

Solve for Bottoms Composition (x_B) and L/V Ratio

Use the McCabe-Thiele graph or iterative balances through the stripping section to find x_B. Similarly, determine the L/V ratio in the stripping section (via a line from x_B matching the end equilibrium state).
07

Calculate Moles of Bottoms per Hour

Using F = 100 kmol/h and D = D_x = 90 kmol/h, solve for B in B = F - D . Factor in flows changed by plate failure.
08

Adjustments After Plates Fail

Without plates 5, 6, 7, recalculate x_B considering fewer theoretical stages. The product composition still leads rectifying calculations but the new stripping section is much less efficient.
09

Using 80 mol% A as Reflux

The new reflux (80 mol% A) shifts operating lines. Recalculate using 80% in reflux: expect composition shifts in distillate and bottoms, requiring transfer to McCabe-Thiele method again.

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

McCabe-Thiele method
The McCabe-Thiele method is a graphical design technique widely used in chemical engineering to estimate how effectively a distillation column can separate components. It's especially effective for binary mixtures. This method involves plotting the equilibrium curve of the mixture and the respective operating lines to visualize the number of required stages for the desired separation.
  • Start by plotting an equilibrium curve that represents the vapor-liquid equilibrium data.
  • Add operating lines for the rectifying and stripping sections using the reflux ratio, which defines the slope of these lines.
  • The intersection of the operating line with the equilibrium curve represents a theoretical stage needed for separation.
Whether you're dealing with this method for a stable column or recalculating after changes, such as the failure of plates, this graphical tool gives a clear insight into how many theoretical stages are required under given conditions. It's a robust method because it visualizes changes like altered feed quality or modified reflux ratios.
Equilibrium curve plot
The equilibrium curve plot is a crucial part of the McCabe-Thiele method. This plot visually represents how the compositions of vapor and liquid are related as they come into equilibrium at different stages in the distillation process.
  • Using the given equilibrium data, plot the mole fractions of component A in the vapor phase (y-axis) versus the liquid phase (x-axis).
  • The equilibrium line typically bows downwards, reflecting how vapor composition changes at near-optimal separation.
  • This curve acts as a basis to optimize the operating lines which affect the efficiency and the number of stages in the distillation column.
It facilitates understanding how changes in feed or reflux conditions will push the system towards or away from efficient separation. The plot is essential for visualizing the impact of disturbances, like falling plates, on the separation process.
Mass and energy balances
Mass and energy balances are fundamental concepts used to ensure conservation principles are followed in the distillation process. In the context of this exercise, mass balances focus on how the feed, distillate, and bottoms relate.
  • The overall mass balance is defined by the equation: \ F = D + B \ where \( F \) is the feed, \( D \) is the distillate, and \( B \) is the bottoms.
  • You also have to perform a component balance to maintain the mole balance of the component within the product streams: \ Fz_F = Dx_D + Bx_B. \
  • Knowing how energy moves within the column complements these mass balances by ensuring efficient heat supply to separate components properly.
Mass balance calculations help determine how disturbances like lost stages or alternative reflux sources affect the column's efficiency by shifting the balance calculations.
Material balance calculations
Material balance calculations in distillation are crucial to determine how changing the input or operational conditions impacts the product compositions. These balances are the practical tools used alongside the McCabe-Thiele method to quantify distillate and bottoms flow rates and compositions.
  • Apply the overall and component balances to find unknown stream flows or compositions.
  • In scenarios like lost plates, material balances show how the reduced number of theoretical stages impacts the concentration of components in the bottom product (\( x_B \)).
  • Incorporating alternative reflux compositions, such as with an 80 mol% A product, involves recalculating the operational efficiencies and expected output compositions.
These material balances allow engineers to project and adjust to physical changes in the equipment or feed conditions, ensuring the operation remains efficient and the desired product purity is achieved.

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Most popular questions from this chapter

A saturated-liquid mixture containing 70 mol% benzene an 30 mol% toluene is to be distilled at atmospheric pressure to prc duce a distillate of 80 mol% benzene. Five procedures, describe below, are under consideration. For each of the procedures, calci late and tabulate: (a) Moles of distillate per 100 moles of feed, (b) Moles of total vapor generated per mole of distillate, (c) Mole percent benzene in the residue, and (d) For each part, construct a y-x diagram. On this, indicate th compositions of the overhead product, the reflux, and the composj tion of the residue. (e) If the objective is to maximize total benzene recovery, which, i any, of these procedures is preferred? Note: Assume that the relative volatility equals 2.5. The procedures are as follows: 1\. Continuous distillation followed by partial condensatior The feed is sent to the direct-heated still pot, from which th residue is continuously withdrawn. The vapors enter the to of a helically coiled partial condenser that discharges intl a trap. The liquid is returned (refluxed) to the still, whil the residual vapor is condensed as a product containin, 80 mol% benzene. The molar ratio of reflux to product is 0.5 2\. Continuous distillation in a column containing one equilib rium plate. The feed is sent to the direct-heated still, fron which residue is withdrawn continuously. The vapors fron the plate enter the top of a helically coiled partial condense that discharges into a trap. The liquid from the trap is re turned to the plate, while the uncondensed vapor is con densed to form a distillate containing 80 mol% benzene The molar ratio of reflux to product is 0.5. 3\. Continuous distillation in a column containing the equivalen of two equilibrium plates. The feed is sent to the direct-heate( still, from which residue is withdrawn continuously. The vapors from the top plate enter the top of a helically coiled partial condenser that discharges into a trap. The liquid from the trap is returned to the top plate (refluxed) while the uncondensed vapor is condensed to form a distillate containing 80 mol% benzene. The molar ratio of reflux to product is 0.5. 4\. The operation is the same as that described for Procedure 3 with the exception that the liquid from the trap is retumed to the bottom plate. 5\. Continuous distillation in a column containing the equivalent of one equilibrium plate. The feed at its boiling point is illtroduced on the plate. The residue is withdrawn continuously from the direct-heated still pot. The vapors from the plate enter the top of a helically coiled partial condenser that discharges into a trap. The liquid from the trap is returned to the plate while the uncondensed vapor is condensed to form a distillate containing 80 mol% benzene. The molar ratio of reflux to product is 0.5.

Prior to the 1980s, packed columns were rarely used for distillation unless column diameter was less than 2.5 ft. Explain why, in recent years, some existing trayed towers are being retrofitted With packing and some new large-diameter columns are being designed for packing rather than trays.

Under what circumstances would it be advisable to conduct laboratory or pilot-plant tests of a proposed distillation separation?

Following the development by Sore1 in 1894 of a mathematical model for continuous, steady-state, equilibrium-stage distillation, a number of methods were proposed for solving the equations graphically or algebraically during an 18-year period from 1920 to 1938, prior to the availability of digital computers. Today, the only method from that era that remains in widespread use is the McCabe-Thiele method. What are the attributes of this method that are responsible for its continuing popularity?

List as many differences between absorption and distillation as you can. List as many differences between stripping and distillation as you can

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