/*! 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 67 The following diagram shows a st... [FREE SOLUTION] | 91影视

91影视

The following diagram shows a staged absorption column in which \(n\) -hexane (H) is absorbed from a gas into a heavy oil.A gas feed stream containing 5.0 mole \(\%\) hexane vapor and the balance nitrogen enters at the bottom of an absorption column at a basis rate of \(100 \mathrm{mol} / \mathrm{s}\), and a nonvolatile oil enters the top of the column in a ratio 2 mol oil fed/mol gas fed. The absorber consists of a series of ideal stages (see Problem 6.66), arranged so that gas flows upward and liquid flows downward. The liquid and gas streams leaving each stage are in equilibrium with each other (by the definition of an ideal stage), with compositions related by Raoult's law. The absorber operates at an approximately constant temperature \(T\left(^{\circ} \mathrm{C}\right)\) and \(760 \mathrm{mm}\) Hg. Of the hexane entering the column, \(99.5 \%\) is absorbed and leaves in the liquid column effluent. At the given conditions it may be assumed that \(\mathrm{N}_{2}\) is insoluble in the oil and that none of the oil vaporizes.(a) Calculate the molar flow rates and mole fractions of hexane in the gas and liquid streams leaving the column. Then calculate the average values of the liquid and gas molar flow rates in the column, \(\dot{n}_{\mathrm{L}}(\mathrm{mol} / \mathrm{s})\) and \(\dot{n}_{\mathrm{G}}(\mathrm{mol} / \mathrm{s}) .\) For simplicity, in subsequent calculations use the average values for liquid and gas molar flow rates within the column, but the actual values for the corresponding flow rates entering and leaving the column.(b) Considering the bottom stage to be ideal, estimate the mole fractions of hexane in the gas leaving that stage \(\left(y_{N}\right)\) and in the liquid entering it \(\left(x_{N-1}\right)\) if the column temperature is \(50^{\circ} \mathrm{C}\). (c) Suppose that \(x_{i}\) and \(y_{i}\) are the mole fractions of hexane in the liquid and gas streams leaving stage \(i\) Derive the following equations from an equilibrium relationship and a mass balance around a section of the column encompassing stage \(i\) and the bottom of the column:$$\begin{array}{c}y_{i}=x_{i} p_{i}^{*}(T) / P \\ x_{i-1}=\left(x_{N} n_{L, N}+y_{i} \dot{n}_{\mathrm{G}}-y_{N+1} \dot{n}_{\mathrm{G}+1}\right) / \dot{n}_{\mathrm{L}}\end{array}$$Verify that these equations yield the answers you calculated in Part (b). (d) Examine the effect of operating temperature on the column by estimating the number of ideal stages necessary to achieve the desired separation. In the calculations, which will be done using a spreadsheet, take the pressure in the column to be constant at 760 torr, but consider three different operating temperatures: \(30^{\circ} \mathrm{C}\) \(50^{\circ} \mathrm{C},\) and \(70^{\circ} \mathrm{C} .\) The calculations will follow a stage-to-stage strategy beginning at the bottom of the column and repeatedly applying Equations (1) and (2) until the mole fraction of hexane in the vapor leaving the column is less than or equal to that calculated in Part (a). You may use APEx or the Antoine equation and Table B.4 to estimate the hexane vapor pressure. The calculations for the case of \(T=30^{\circ} \mathrm{C}\) illustrate how to proceed; for this case, \(y_{N-1} < y_{1}=0.00263\) after only two stages.(e) You can see that the number of stages required increases as the column temperature increases. In fact, there is a maximum temperature beyond which the required separation cannot be achieved. At that temperature, the entering gas and leaving liquid are approximately in equilibrium, so that \(x_{N} p^{*}(T)=y_{N+1} P .\) Use either APEx or the Antoine equation to estimate the maximum temperature at which the separation can be achieved.

Short Answer

Expert verified
The molar flow rates and mole fractions of hexane in the gas and liquid streams leaving the column are 0.025 mol/s, 4.975 mol/s, 0.000263 and 0.0243 respectively. The average liquid and gas molar flow rates within the column are 202.488 mol/s and 95.013 mol/s respectively. The number of ideal stages for separation at \(T=30^{\circ}C\), \(50^{\circ}C\) and \(70^{\circ}C\) will differ depending on the constant column pressure and the hexane vapor pressure at these temperatures, as computed with the Antoine equation. The maximum temperature for separation can be derived using equilibrium conditions and the Antoine equation.

Step by step solution

01

Calculation of Molar Flow Rates and Mole Fractions of Hexane in the Streams Leaving the Column

Firstly, find the molar flow rates of hexane entering the absorption column from the gas feed and the oil feed, denoted as \(n_{H,G}^{in}\) and \(n_{O}^{in}\) respectively. Given \(n_{H,G}^{in} = 0.05 * 100 mol/s = 5 mol/s \) and \(n_{O}^{in} = 2 * 100 mol/s = 200 mol/s \). Now, calculate the hexane absorbed, \(n_{H}^{abs} = 0.995 * 5 mol/s = 4.975 mol/s \). Thus, the molar flow rate of hexane in the liquid stream leaving the column, \(n_{H,L}^{out} = n_{H}^{abs} = 4.975 mol/s \). And molar flow rate of hexane in the gas stream leaving the column, \(n_{H,G}^{out} = n_{H,G}^{in} - n_{H}^{abs} = 0.025 mol/s \). Similarly, find the molar flow rates of N2 and oil leaving the column, \(n_{N2}^{out} = n_{N2}^{in} = 100 - n_{H,G}^{in} = 95 mol/s \) and \(n_{O}^{out} = n_{O}^{in} = 200 mol/s \). Hence, the molar flow rates leaving the column in the gas stream \(\dot{n}_{G}^{out} = n_{N2}^{out} + n_{H,G}^{out} = 95 + 0.025 = 95.025 mol/s \) and in the liquid stream \(\dot{n}_{L}^{out} = n_{O}^{out} + n_{H,L}^{out} = 200 + 4.975 = 204.975 mol/s \). Calculate mole fractions of hexane in the gas and liquid streams leaving the column as \(y_{N+1} = n_{H,G}^{out} / \dot{n}_{G}^{out} = 0.025 / 95.025 = 0.000263 \) and \(x_{N} = n_{H,L}^{out} / \dot{n}_{L}^{out} = 4.975 / 204.975 = 0.0243 \) respectively.
02

Calculation of Average Values of the Liquid and Gas Molar Flow Rates in the Column

Next, compute the average values of the liquid and gas molar flow rates in the column as \(\dot{n}_{L} = (\dot{n}_{L}^{out} + n_{O}^{in}) / 2 = (204.975 + 200) / 2 = 202.488 mol/s \) and \(\dot{n}_{G} = (\dot{n}_{G}^{out} + n_{N2}^{out}) / 2 = (95.025 + 95) / 2 = 95.013 mol/s \) respectively.
03

Calculation of Mole Fractions of Hexane in the Bottom Stage

Use Raoult's law and the derived relationship for \(x_{i-1}\) from the equilibrium relationship and the mass balance to compute \(y_{N}\) and \(x_{N-1}\). For \(T=50^{\circ} C\), use the Antoine equation or APEx to determine \(p_{N}^{*}(50) \). Then find \(y_{N}\) from \(y_{i} = x_{i} p_{i}^{*}(T) / P \) and \(x_{N-1}\) from \(x_{i-1} = \left(x_{N} n_{L, N} + y_{i} \dot{n}_{G} - y_{N+1} \dot{n}_{G+1}\right) / \dot{n}_{L} \).
04

Estimation of Number of Ideal Stages to Achieve Desired Separation

Examine the effect of operating temperature by computing the number of ideal stages necessary for separation at \(T = 30^{\circ} C \), \(50^{\circ} C \) and \(70^{\circ} C \). Using the Antoine equation for hexane vapor pressure \(p^{*}(T) \) at each of these temperatures, apply the derived relationships \(y_{i} = x_{i} p_{i}^{*}(T) / P \) and \(x_{i-1} = \left(x_{N} n_{L, N} + y_{i} \dot{n}_{G} - y_{N+1} \dot{n}_{G+1}\right) / \dot{n}_{L} \) until \(y_{N-1} \leq y_{1} = 0.000263 \) is satisfied. The number of applications corresponds to the number of ideal stages.
05

Estimation of Maximum Temperature for Desired Separation

The maximum temperature at which separation is achievable is the temperature at which the entering gas and leaving liquid are in equilibrium. Derive this temperature by setting \(x_{N} p^{*}(T) = y_{N+1} P \), then using either the Antoine equation or APEx to solve for \(T \).

Unlock Step-by-Step Solutions & Ace Your Exams!

  • Full Textbook Solutions

    Get detailed explanations and key concepts

  • Unlimited Al creation

    Al flashcards, explanations, exams and more...

  • Ads-free access

    To over 500 millions flashcards

  • Money-back guarantee

    We refund you if you fail your exam.

Over 30 million students worldwide already upgrade their learning with 91影视!

Key Concepts

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

Hexane Absorption
Hexane absorption is a key process used in chemical engineering to separate hexane from a gas mixture.
In an absorption column, a volatile component like hexane is extracted from a gas stream using a non-volatile liquid solvent, often referred to as the absorbent.
The gas containing hexane enters from the bottom of the column, and the absorbing liquid flows downward.
As they come into contact, hexane transfers from the gas phase to the liquid phase. The effectiveness of hexane absorption depends on various factors:
  • The flow rates of the gas and liquid streams. Higher flow rates typically lead to better contact between phases.
  • The temperature within the column, which affects the solubility and vapor pressures.
  • The design of the column, including the number of stages or trays that enhance the contact between gas and liquid.
This process has extensive applications across industries such as petrochemical and environmental engineering, where precise separation is crucial.
Raoult's Law
Raoult's Law is a principle used to predict the vapor pressure of a solvent in a solution.
It states that the partial vapor pressure of each component in a volatile liquid mixture is proportional to its mole fraction in the mixture and its pure component vapor pressure.
For a component 'i' in a liquid solution, Raoult's Law is given by:\[ p_i = x_i imes p_i^* \] where:
  • \( p_i \) is the partial pressure of component 'i'.
  • \( x_i \) is the mole fraction of component 'i' in the liquid phase.
  • \( p_i^* \) is the vapor pressure of the pure component 'i' at a given temperature.
In the context of an absorption column, Raoult's Law helps relate the composition of hexane in the liquid phase to its concentration in the gas phase under equilibrium conditions.
This relationship guides the design and analysis of the absorption column by predicting how much hexane can be absorbed at a given temperature and pressure.
Equilibrium Stages
Equilibrium stages are theoretical zones in an absorption column where the liquid and gas phases are in perfect equilibrium.
Here, the compositions of the liquid and gas are calculated under the assumption that they have reached a balance in terms of mass and energy exchange. In an ideal absorption column, each stage represents a complete equilibrium between the entering and exiting streams. This means:
  • The composition of hexane in the gas phase leaving each stage is in thermal and chemical equilibrium with the liquid phase leaving the same stage.
  • Raoult's Law can be applied at each stage to solve for compositions based on known pressures and temperatures.
The number of equilibrium stages needed to achieve a desired separation is a crucial aspect of design, often determined using graphical techniques like McCabe-Thiele diagrams. The greater the number of stages, the more effective the separation, but also, the more complex and costly the column.
Therefore, accurate estimation of equilibrium stages is key for cost-effective and efficient absorption column operation.
Molecular Flow Rates
Molecular flow rates are essential in understanding the dynamics of fluid movement within an absorption column.
These rates provide insight into how much of each component moves through the system over a unit of time and helps in setting up material balances which are pivotal for process design. For hexane absorption, molecular flow rates will be quantified for both:
  • The gas stream, including components like hexane and nitrogen.
  • The liquid stream, including the absorbing oil and absorbed hexane.
The flow rates are calculated based on known feed conditions and the separation efficiency of the column.
They are used to determine the molar composition in output streams and to assess the efficiency of the absorption process. Knowing these rates allows engineers to scale-up the process from pilot scale to industrial scale and to optimize for variables such as operating pressure, temperature, and flow velocities to ensure efficient separation within the absorption column.

One App. One Place for Learning.

All the tools & learning materials you need for study success - in one app.

Get started for free

Most popular questions from this chapter

Various amounts of activated carbon were added to a fixed amount of raw cane sugar solution \((48 \mathrm{wt} \%\) sucrose in water) at \(80^{\circ} \mathrm{C} .\) A colorimeter was used to measure the color of the solutions, \(R,\) which is proportional to the concentration of trace unknown impurities in the solution. The following data were obtained (adapted from the reference in Footnote \(20,\) p. 652 ):$$\begin{array}{|l|r|r|r|r|r|r|} \hline \text { kg carbon/kg dry sucrose } & 0 & 0.005 & 0.010 & 0.015 & 0.020 & 0.030 \\ \hline R \text { (color units/kg sucrose) } & 20.0 & 10.6 & 6.0 & 3.4 & 2.0 & 1.0 \\ \hline\end{array}.$$ The reduction in color units is a measure of the mass of impurities (the adsorbate) adsorbed on the carbon (the adsorbent).(a) The general form of the Freundlich isotherm is $$X_{i}^{*}=K_{\mathrm{F}} c_{i}^{\beta}$$ where \(X_{i}^{*}\) is the mass of \(i\) adsorbed/mass of adsorbent and \(c_{i}\) is the concentration of \(i\) in solution. Demonstrate that the Freundlich isotherm may be formulated for the system described above as $$\vartheta=K_{\mathrm{F}}^{\prime} R^{\beta}$$ where \(\vartheta\) is the \(\%\) removal of color/[mass of carbon/mass of dissolved sucrose]. Then determine \(K_{\mathrm{F}}^{\prime}\) and \(\beta\) by fitting this expression to the given data, using one of the methods in Section \(2.7 .\) (b) Calculate the amount of carbon that would have to be added to a vat containing \(1000 \mathrm{kg}\) of the 48 wt\% sugar solution at \(80^{\circ} \mathrm{C}\) for a reduction in color content to \(2.5 \%\) of the original value.

In an attempt to conserve water and to be awarded LEED (Leadership in Energy and Environmental Design) certification, a 20,000-liter cistem has been installed during construction of a new building. The cistem collects water from an HVAC (heating, ventilation, and air-conditioning) system designed to provide 2830 cubic meters of air per minute at \(22^{\circ} \mathrm{C}\) and \(50 \%\) relative humidity after converting it from ambient conditions \(\left(31^{\circ} \mathrm{C}, 70 \% \text { relative humidity }\right) .\) The collected condensate serves as the source of water for lawn maintenance. Estimate (a) the rate of intake of air at ambient conditions in cubic feet per minute and (b) the hours of operation required to fill the cistern.

Using Raoult's law or Henry's law for each substance (whichever one you think appropriate), calculate the pressure and gas-phase composition (mole fractions) in a system containing a liquid that is 0.3 mole \(\% \mathrm{N}_{2}\) and 99.7 mole \(\%\) water in equilibrium with nitrogen gas and water vapor at \(80^{\circ} \mathrm{C}\).

The vapor pressure of an organic solvent is \(50 \mathrm{mm}\) Hg at \(25^{\circ} \mathrm{C}\) and \(200 \mathrm{mm} \mathrm{Hg}\) at \(45^{\circ} \mathrm{C}\). The solvent is the only species in a closed flask at \(35^{\circ} \mathrm{C}\) and is present in both liquid and vapor states. The volume of gas above the liquid is \(150 \mathrm{mL}\). (a) Estimate the amount of the solvent \((\mathrm{mol})\)contained in the gas phase. (b) What assumptions did you make? How would your answer change if the species dimerized (one molecule results from two molecules of the species combining)?

A liquid mixture contains \(N\) components ( \(N\) may be any number from 2 to 10 ) at pressure \(P(\mathrm{mm} \mathrm{Hg})\). The mole fraction of the ith component is \(x_{i}(i=1,2, \ldots, N),\) and the vapor pressure of that component is given by the Antoine equation (see Table B.4) with constants \(A_{i}, B_{i},\) and \(C_{i}\). Raoult's law may be applied to each component.(a) Write the equations you would use to calculate the bubble-point temperature of the mixture, ending with an equation of the form \(f(T)=0 .\) (The value of \(T\) that satisfies this equation is the bubble-point temperature.) Then write the equations for the component mole fractions \(\left(y_{1}, y_{2}, \ldots, y_{N}\right)\) in the first bubble that forms, assuming that the temperature is now known.(b) Prepare a spreadsheet to perform the calculations of Part (a). The spreadsheet should include a title line for identification of the problem and a row that has entries for the given pressure and an estimate of the system temperature. Be sure to label these variables and show the units in which each is expressed. Adjacent columns should be headed Species, \(p_{i}^{*}, x_{i}, p_{i},\) and \(y_{i} .\) Values of vapor pressures at the estimated temperature should be calculated using the physical property database in APEx, and Raoult's law should be used to determine partial pressures. The final row in the table should have the sums of the vapor mole fractions and partial pressures. Place a convergence function \(f(T)=P-\Sigma p_{i}\) below the table so that Goal Seek can be used to vary the estimated \(T\) until \(f(T)=0 .\) Test the spreadsheet by calculating the bubble-point temperature for a liquid mixture containing 22.6 mole \(\%\) benzene, \(22.6 \%\) ethylbenzene, \(22.3 \%\) toluene, and the balance styrene at pressures of \(250 \mathrm{mm} \mathrm{Hg}, 760 \mathrm{mm} \mathrm{Hg},\) and \(7500 \mathrm{mm}\) Hg. Identify any concerns you may have about the calculated results.(c) It is determined that instead of styrene, the balance of the above mixture in Part (b) is propylbenzene. Upon entering the name "propylbenzene鈥 in the APEx AntoineP estimator, you probably get the error message #VALUE!, which means that this substance is not in the APEx database. Poling et al. (see Footnote 2, p. A.57) provide constants for the vapor pressure of propylbenzene corresponding to the following expression of the Antoine equation:$$\log _{10} p^{*}(\mathrm{bar})=A-B /\left[T\left(^{\circ} \mathrm{C}\right)+C\right]$$ where \(A=4.07664, B=1491.8,\) and \(C=207.25 ;\) the correlation is valid over the range \(324 \mathrm{K}-\) 461 K. Modify the spreadsheet to incorporate this expression, and estimate the bubble-point temperature of the mixture at a pressure of \(760 \mathrm{mm} \mathrm{Hg}\).

See all solutions

Recommended explanations on Chemistry Textbooks

View all explanations

What do you think about this solution?

We value your feedback to improve our textbook solutions.

Study anywhere. Anytime. Across all devices.