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A liquid mixture of acetone and water contains 35 mole\% acetone. The mixture is to be partially evaporated to produce a vapor that is 75 mole \(\%\) acetone and leave a residual liquid that is 18.7 mole \(\%\) (a) Suppose the process is to be carried out continuously and at steady state with a feed rate of 10.0 kmol/h. Let \(\dot{n}_{\mathrm{v}}\) and \(\dot{n}_{1}\) be the flow rates of the vapor and liquid product streams, respectively. Draw and label a process flowchart, then write and solve balances on total moles and on acetone to determine the values of \(\dot{n}_{\mathrm{v}}\) and \(\dot{n}_{\mathrm{l}}\). For each balance, state which terms in the general balance equation (accumulation \(=\)input \(+\)generation \(-\)output\(-\)consumption ) can be discarded and why. (See Example 4.2-2.) (b) Now suppose the process is to be carried out in a closed container that initially contains 10.0 kmol of the liquid mixture. Let \(n_{\mathrm{v}}\) and \(n_{1}\) be the moles of final vapor and liquid phases, respectively. Draw and label a process flowchart, then write and solve integral balances on total moles and on acetone. For each balance, state which terms of the general balance equation can be discarded and why. (c) Returning to the continuous process, suppose the vaporization unit is built and started and the product stream flow rates and compositions are measured. The measured acetone content of the vapor stream is 75 mole \(\%\) acetone, and the product stream flow rates have the values calculated in Part (a). However, the liquid product stream is found to contain 22.3 mole \(\%\) acetone. It is possible that there is an error in the measured composition of the liquid stream, but give at least five other reasons for the discrepancy. [Think about assumptions made in obtaining the solution of Part (a).]

Short Answer

Expert verified
For the continuous process, the vapor and liquid flow rates can be determined by solving the mole balances. In the batch process, the final moles of vapor and liquid can be determined also by mole balances, but here considering the closed nature of the process. Possible sources of discrepancies between calculated and real values could be measurement errors, incorrect feed assumption, reactions, non-ideal behavior, equipment inefficiencies or other unknown components in the feed.

Step by step solution

01

Determine Flow Rates for Steady State Continuous Process

First note that in a steady state process, there is no accumulation. Also, there is no generation or consumption of acetone - it is merely being redistributed between the vapor and liquid phases. So the balance equation simplifies to input = output. Let \( x_{f} = 0.35 \) be the mole fraction of acetone in the feed, \( x_{v} = 0.75 \) in the vapor, and \( x_{l} = 0.187 \) in the liquid. Write an overall mole balance for the entire process and an acetone balance. Then solve these two equations to find \( \dot{n}_v \) and \( \dot{n}_l \).
02

Determine Mole Fractions for Batch Process

Now consider this process occurs in a closed container, which means \( n_v \) and \( n_l \) are dependent upon the initial amount of mixture in the container. Therefore, the principle of the mole balance still applies but now the general balance equation simplifies to initial = final. Draw a similar process flowchart as in step 1 and set up integral balances on total moles and on acetone, discarding the terms for input and output. Then solve these equations to find \( n_v \) and \( n_l \).
03

Discuss Possible Discrepancies

Given a scenario where the vaporization unit is built and the results are inconsistent with calculations performed in part (a), identify potential sources for discrepancies. Factors to consider include: measurement errors, assumption of accurate feed composition, neglect of potential reactions, assumption of ideal phases, equipment inefficiencies, and potential presence of other components in the mixture.

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Key Concepts

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

Mole Fraction
In chemistry and process engineering, understanding the concept of mole fraction is crucial because it helps describe the composition of mixtures. The mole fraction of a component in a mixture is defined as the ratio of the number of moles of that component to the total number of moles of all components in the mixture. It's a dimensionless quantity often represented by the symbol \( x \), like \( x_f \) for feed, \( x_v \) for vapor, and \( x_l \) for liquid, in our exercise.

To calculate the mole fraction, you use the formula:
\[ x_i = \frac{n_i}{ ext{total moles}} \]
where \( n_i \) is the moles of the component of interest.

In our example, the feed mixture starts with 35 mole \( \% \) acetone, which means the mole fraction of acetone in the feed is 0.35. Mole fractions are useful because they remain constant across various conditions like pressure and temperature, making them especially important in analyses of chemical processes like vaporization.
Steady State
Steady state is a concept used to describe a condition where the variables (e.g., chemical concentrations, temperatures) remain constant over time in a system, even though there might be the flow of material through the system. In a steady state process, such as in part (a) of our exercise, there is no accumulation of mass within the system because input exactly equals output.

In terms of a balance equation, this means:
\[ ext{accumulation} = ext{input} - ext{output} + ext{generation} - ext{consumption} = 0 \]

Because we have no generation or consumption of acetone, it's about redistribution into vapor and liquid streams without any loss or gain within the system.
  • No change in the amount stored, so steady conditions prevail.
  • Simplifies calculations as we can focus directly on input equals output for each component.
Applying this to our exercise, both total mole balance and acetone mole balance simplify, helping us find flow rates efficiently.
Vaporization Process
Vaporization is the process where a liquid is converted into vapor. A common example is boiling water to produce steam. In industry, vaporization processes are used to separate components based on their volatility. The vaporization process in the exercise involves acetone and water, where control over the composition of vapor and residual liquid is necessary.

Critical factors include:
  • Volatility: The more volatile component will occupy a higher mole fraction in the vapor phase.
  • Energy Input: Adequate heat must be supplied to enable the phase change.
  • Process Design: Equipment like distillation columns can enhance separation efficiency.
In the exercise, the vapor should contain 75 mole \( \% \) acetone, showcasing selective evaporation. Understanding vapor-liquid equilibrium can optimize such processes, indicating the extent to which components will separate under given conditions.
Batch Process
In a batch process, the operation is executed in a closed system where materials are added at the start, and the process runs without adding or removing material, except through the operation itself until the completion. It's characterized by pre-determined processing time and volume.

This differs from continuous processes in configuration and operation:
  • No Flow: Since flow in or out isn't continuous, the system behaves as a self-contained unit.
  • Initial to Final: You must determine the state change from the initial condition to the final state. It's often expressed as "initial = final" in mole balances.
  • Flexibility: Easier to adjust conditions for small-scale production.
In part (b) of the exercise, this involves recalculating for a static mass within the container, making integral (rather than differential) balance equations suitable. The approach requires understanding the total closed system dynamics, ensuring proper redistribution during the vaporization phase.

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Most popular questions from this chapter

Methanol is produced by reacting carbon monoxide and hydrogen. A fresh feed stream containing \(\mathrm{CO}\) and \(\mathrm{H}_{2}\) joins a recycle stream and the combined stream is fed to a reactor. The reactor outlet stream flows at a rate of \(350 \mathrm{mol} / \mathrm{min}\) and contains \(10.6 \mathrm{wt} \% \mathrm{H}_{2}, 64.0 \mathrm{wt} \% \mathrm{CO},\) and \(25.4 \mathrm{wt} \% \mathrm{CH}_{3} \mathrm{OH} .\) (Notice that those are percentages by mass, not mole percents.) This stream enters a cooler in which most of the methanol is condensed. The liquid methanol condensate is withdrawn as a product, and the gas stream leaving the condenser- -which contains \(\mathrm{CO}, \mathrm{H}_{2},\) and \(0.40 \mathrm{mole} \%\) uncondensed \(\mathrm{CH}_{3} \mathrm{OH}\) vapor \(-\mathrm{is}\) the recycle stream that combines with the fresh feed. (a) Without doing any calculations, prove that you have enough information to determine (i) the molar flow rates of CO and \(\mathrm{H}_{2}\) in the fresh feed, (ii) the production rate of liquid methanol, and (iii) the single-pass and overall conversions of carbon monoxide. Then perform the calculations. (b) After several months of operation, the flow rate of liquid methanol leaving the condenser begins to decrease. List at least three possible explanations of this behavior and state how you might check the validity of each one. (What would you measure and what would you expect to find if the explanation is valid?)

Oxygen consumed by a living organism in aerobic reactions is used in adding mass to the organism and/or the production of chemicals and carbon dioxide. since we may not know the molecular compositions of all species in such a reaction, it is common to define the ratio of moles of \(\mathrm{CO}_{2}\) produced per mole of \(\mathrm{O}_{2}\) consumed as the respiratory quotient, \(R Q,\) where $$R Q=\frac{n_{\mathrm{CO}_{2}}}{n_{\mathrm{O}_{2}}}\left(\text { or } \frac{\dot{n}_{\mathrm{CO}_{2}}}{\dot{n}_{\mathrm{O}_{2}}}\right)$$ since it generally is impossible to predict values of \(R Q\), they must be determined from operating data. Mammalian cells are used in a bioreactor to convert glucose to glutamic acid by the reaction $$\mathrm{C}_{6} \mathrm{H}_{12} \mathrm{O}_{6}+a \mathrm{NH}_{3}+b \mathrm{O}_{2} \rightarrow p \mathrm{C}_{5} \mathrm{H}_{9} \mathrm{NO}_{4}+q \mathrm{CO}_{2}+r \mathrm{H}_{2} \mathrm{O}$$ The feed to the bioreactor comprises \(1.00 \times 10^{2} \mathrm{mol} \mathrm{C}_{6} \mathrm{H}_{12} \mathrm{O}_{6} / \mathrm{day}, 1.20 \times 10^{2} \mathrm{mol} \mathrm{NH}_{3} / \mathrm{day},\) and \(1.10 \times\) \(10^{2}\) mol \(\mathrm{O}_{2} /\) day. Data on the system show that \(R Q=0.45 \mathrm{mol} \mathrm{CO}_{2}\) produced/mol \(\mathrm{O}_{2}\) consumed. (a) Determine the five stoichiometric coefficients and the limiting reactant. (b) Assuming that the limiting reactant is consumed completely, calculate the molar and mass flow rates of all species leaving the reactor and the fractional conversions of the non-limiting reactants.

The hormone estrogen is produced in the ovaries of females and elsewhere in the body in men and postmenopausal women, and it is also administered in estrogen replacement therapy, a common treatment for women who have undergone a hysterectomy. Unfortunately, it also binds to estrogen receptors in breast tissue and can activate cells to become cancerous. Tamoxifen is a drug that also binds to estrogen receptors but does not activate cells, in effect blocking the receptors from access to estrogen and inhibiting the growth of breast-cancer cells. Tamoxifen is administered in tablet form. In the manufacturing process, a finely ground powder contains tamoxifen (tam) and two inactive fillers- -lactose monohydrate (lac) and corn starch (cs). The powder is mixed with a second stream containing water and suspended solid particles of polyvinylpymolidone (pvp) binder, which keeps the tablets from easily crumbling. The slurry leaving the mixer goes to a dryer, in which 94.2\% of the water fed to the process is vaporized. The wet powder leaving the dryer contains 8.80 wr\% tam, 66.8\% lac, 21.4\% cs, 2.00\% pvp, and 1.00\% water. After some additional processing, the powder is molded into tablets. To produce a hundred thousand tablets, 17.13 kg of wet powder is required. (a) Taking a basis of 100,000 tablets produced, draw and label a process flowchart, labeling masses of individual components rather than total masses and component mass fractions. It is unnecessary to label the stream between the mixer and the dryer. Carry out a degree-of-freedom analysis of the overall two-unit process. (b) Calculate the masses and compositions of the streams that must enter the mixer to make 100,000 tablets. (c) Why was it unnecessary to label the stream between the mixer and the dryer? Under what circumstances would it have been necessary? (d) Go back to the flowchart of Part (a). Without using the mass of the wet powder (17.13 kg) or any of the results from Part (b) in your calculations, determine the mass fractions of the stream components in the powder fed to the mixer and verify that they match your solution to Part (b). (Hint: Take a basis of \(100 \mathrm{kg}\) of wet powder.) (e) Suppose a student does Part (d) before Part (b), and re-labels the powder feed to the mixer on the flowchart of Part (a) with an unknown total mass ( \(m_{1}\) ) and the three now known mole fractions. (Sketch the resulting flowchart.) The student then does a degree-of-freedom analysis, counts four unknowns (the masses of the powder, pvp, and water fed to the mixer, and the mass of water evaporated in the dryer), and six equations (five material balances for five species and the percentage evaporation), for a net of -2 degrees of freedom. since there are more equations than unknowns, it should not be possible to get a unique solution for the four unknowns. Nevertheless, the student writes four equations, solves for the four unknowns, and verifies that all of the balance equations are satisfied. There must have been a mistake in the degree-of-freedom calculation. What was it?

A fuel oil is analyzed and found to contain 85.0 wt\% carbon, \(12.0 \%\) elemental hydrogen (H), \(1.7 \%\) sulfur, and the remainder noncombustible matter. The oil is burned with \(20.0 \%\) excess air, based on complete combustion of the carbon to \(\mathrm{CO}_{2}\), the hydrogen to \(\mathrm{H}_{2} \mathrm{O}\), and the sulfur to \(\mathrm{SO}_{2}\). The oil is burned completely, but \(8 \%\) of the carbon forms CO. Calculate the molar composition of the stack gas.

Methanol is formed from carbon monoxide and hydrogen in the gas-phase reaction The mole fractions of the reactive species at equilibrium satisfy the relation where \(P\) is the total pressure (atm), \(K_{c}\) the reaction equilibrium constant (atm \(^{-2}\) ), and \(T\) the temperature (K). The equilibrium constant \(K_{c}\) equals 10.5 at 373 K, and \(2.316 \times 10^{-4}\) at \(573 \mathrm{K}\). A semilog plot of \(K_{\mathrm{c}}\) (logarithmic scale) versus 1/ \(T\) (rectangular scale) is approximately linear between \(T=300 \mathrm{K}\) and \(T=600 \mathrm{K}\) (a) Derive a formula for \(K_{\mathrm{c}}(T),\) and use it to show that \(K_{\mathrm{e}}(450 \mathrm{K})=0.0548 \mathrm{atm}^{-2}\) (b) Write expressions for \(n_{A}, n_{B},\) and \(n_{C}\) (gram-moles of each species), and then \(y_{A}, y_{B},\) and \(y_{C},\) in terms of \(n_{\mathrm{A} 0}, n_{\mathrm{B} 0}, n_{\mathrm{C} 0},\) and \(\xi,\) the extent of reaction. Then derive an equation involving only \(n_{\mathrm{A} 0}, n_{\mathrm{B} 0}, n_{\mathrm{C} 0}, P, T,\) and \(\xi_{e},\) where \(\xi_{e}\) is the extent of reaction at equilibrium. (c) Suppose you begin with equimolar quantities of CO and \(\mathrm{H}_{2}\) and no \(\mathrm{CH}_{3} \mathrm{OH}\), and the reaction proceeds to equilibrium at 423 K and 2.00 atm. Calculate the molar composition of the product ( \(y_{\mathrm{A}}\), \(\left.y_{\mathrm{B}}, \text { and } y_{\mathrm{C}}\right)\) and the fractional conversion of \(\mathrm{CO}\) (d) The conversion of CO and \(\mathrm{H}_{2}\) can be enhanced by removing methanol from the reactor while leaving unreacted CO and \(\mathrm{H}_{2}\) in the vessel. Review the equations you derived in solving Part (c) and determine any physical constraints on \(\xi_{c}\) associated with \(n_{\mathrm{A} 0}=n_{\mathrm{B} 0}=1\) mol. Now suppose that 90\% of the methanol is removed from the reactor as it is produced; in other words, only 10\% of the methanol formed remains in the reactor. Estimate the fractional conversion of CO and the total gram moles of methanol produced in the modified operation. (e) Repeat Part (d), but now assume that \(n_{\mathrm{B} 0}=2\) mol. Explain the significant increase in fractional conversion of CO. (f) Write a set of equations for \(y_{\mathrm{A}}, y_{\mathrm{B}}, y_{\mathrm{C}},\) and \(f_{\mathrm{A}}\) (the fractional conversion of \(\mathrm{CO}\) ) in terms of \(y_{\mathrm{A} 0}, y_{\mathrm{B} 0}, T,\) and \(P(\) the reactor temperature and pressure at equilibrium). Enter the equations in an equation-solving program. Check the program by running it for the conditions of Part (c), then use it to determine the effects on \(f_{\mathrm{A}}\) (increase, decrease, or no effect) of separately increasing, (i) the fraction of \(\mathrm{CH}_{3} \mathrm{OH}\) in the feed, (ii) temperature, and (iii) pressure.

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