/*! 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 3 A liquid-phase chemical reaction... [FREE SOLUTION] | 91Ó°ÊÓ

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A liquid-phase chemical reaction \(\mathrm{A} \rightarrow \mathrm{B}\) takes place in a well-stirred tank. The concentration of \(\mathrm{A}\) in the feed is \(C_{\mathrm{A} 0}\left(\operatorname{mol} / \mathrm{m}^{3}\right),\) and that in the tank and outlet stream is \(C_{\mathrm{A}}\left(\mathrm{mol} / \mathrm{m}^{3}\right) .\) Neither concentration varies with time. The volume of the tank contents is \(V\left(\mathrm{m}^{3}\right)\) and the volumetric flow rate of the inlet and outlet streams is \(\dot{V}\left(\mathrm{m}^{3} / \mathrm{s}\right)\). The reaction rate (the rate at which \(\mathrm{A}\) is consumed by reaction in the tank) is given by the expression $$r(\text { mol } A \text { consumed } / \mathrm{s})=k V C_{\mathrm{A}}$$ (a) Is this process continuous, batch, or semibatch? Is it transient or steady-state? (b) What would you expect the reactant concentration \(C_{\mathrm{A}}\) to equal if \(k=0\) (no reaction)? What should it approach if \(k \rightarrow \infty\) (infinitely rapid reaction)? (c) Write a differential balance on \(A,\) stating which terms in the general balance equation (accumulation = input + generation - output - consumption) you discarded and why you discarded them. Use the balance to derive the following relation between the inlet and outlet reactant concentrations: $$C_{\mathrm{A}}=\frac{C_{\mathrm{A} 0}}{1+k V / \dot{V}}$$ Verify that this relation predicts the results in Part (b).

Short Answer

Expert verified
From the analysis, it can be established that this process is a continuous and steady-state process. The derived relation for the tank concentration is \(C_A=\frac{C_{A0}}{1+kV/\dot{V}}\) which is verified for the limits of reaction rate constant k.

Step by step solution

01

Identify Process Type

From the problem statement, it can be inferred that the concentration in the tank does not vary with time and neither does it in the outlet and inlet streams. Therefore, this is a steady-state process. Moreover, the same flow rate for the inlet and outlet implies a flow in and out of the tank. This makes it a continuous process.
02

Reactant Concentration at Different Reaction Rates

If \(k=0\) meaning there is no reaction, no A is consumed. Hence, the inlet concentration would be the same as the tank and outlet concentrations. So, \(C_A=C_{A0}\). If \(k \rightarrow \infty\), the reaction would be infinitely fast. That means A would react out as soon as it enters the tank and the concentration in the tank would theoretically approach zero.
03

Write Differential Balance for A

For a steady-state process, accumulation term is zero. The generation term will be zero as A is not generated in the tank. Hence, the balance equation becomes: 0 = Input - Output - Consumption. Substituting the terms, we get \(0= C_{A0}\dot{V}-C_A\dot{V}-kVC_A \). Divide the equation by \( V\dot{V}\) to simplify it.
04

Derive the Relation

The simplified balance equation becomes: \(0= C_{A0} -C_A-kC_A\). By rearranging the terms, it yields \(C_A=\frac{C_{A0}}{1+kV/\dot{V}}\).
05

Verify the Derived Relation

For \(k=0\), substituting in derived equation gives \(C_A=C_{A0}\), which verifies for the condition of no reaction. For \(k \rightarrow \infty\), the denominator of the fraction in the derived relation becomes infinitely large making \(C_A=0\), which verifies for the condition of an infinitely fast reaction.

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Key Concepts

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

Reactor Design
Reactor design is a fundamental aspect of chemical reaction engineering that involves determining the most suitable type of reactor to conduct a specific chemical reaction efficiently and safely. There are various types of reactors, such as batch, continuous-stirred tank reactors (CSTR), plug flow reactors (PFR), and packed bed reactors, each suitable for different processes and reaction kinetics.

In our exercise, the reactor in question is a well-stirred tank, typically known as a CSTR, which is used for liquid-phase reactions. The design of such a reactor ensures complete mixing, implying uniform concentration and temperature throughout the reactor. The choice between a batch and continuous reactor depends on the desired operation mode, which affects the scalability, cost, and reaction control. In the given scenario, the reactor operates in a continuous mode as the feed is constantly supplied and products are removed, keeping the volume within the reactor constant over time. Understanding reactor design elements is crucial for optimizing reaction conditions, ensuring product quality, and scaling up processes in the industry.
Steady-State Process
A steady-state process is one where the variables (such as temperature, pressure, concentration) do not change with time. In the context of a chemical reactor, a steady-state operation means that the concentrations of reactants and products in the reactor remain constant over time, regardless of the changes that may occur in the feed. This implies that the rate of addition of reactants is balanced by the rate of removal of products and unreacted reactants.

In the example provided, the process is identified as steady-state due to the constant concentrations of reactant A in the feed and in the tank. This implies a balance between the input and output flows, which is characteristic of process industries striving for continuous production. Understanding steady-state conditions is vital for simplifying the calculations of reactor sizing and for analysis because it eliminates the time dependency, allowing for the use of algebraic equations instead of differential ones. The steady-state assumption is advantageous in industrial applications because it enables consistent product quality and simplifies control strategies.
Differential Balance
Differential balance, or material balance, is used to quantify how much of a reactant is present, being produced, consumed, or removed from a system over a period of time. The general balance equation includes terms for accumulation, input, generation, output, and consumption. However, in a steady-state process, the accumulation term is zero because the amount of material in the system isn't changing with time.

As for the given exercise, we are asked to consider a differential balance on species A. Since the process is at a steady-state and the reactor is well-mixed, there is no generation of A within the reactor. Therefore, the terms for accumulation and generation are discarded in the balance. What remains is to balance the input and output of A with its consumption by the reaction. Simplifying the equation and dividing by terms including flowrate and volume leads to a key relationship between the inlet concentration and the outlet concentration of A. This equation is invaluable for engineers as it succinctly relates kinetic parameters and process variables, enabling them to manipulate and control reactor systems optimally.

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Most popular questions from this chapter

Carbon nanotubes (CNT) are among the most versatile building blocks in nanotechnology. These unique pure carbon materials resemble rolled-up sheets of graphite with diameters of several nanometers and lengths up to several micrometers. They are stronger than steel, have higher thermal conductivities than most known materials, and have electrical conductivities like that of copper but with higher currentcarrying capacity. Molecular transistors and biosensors are among their many applications. While most carbon nanotube research has been based on laboratory-scale synthesis, commercial applications involve large industrial-scale processes. In one such process, carbon monoxide saturated with an organo-metallic compound (iron penta-carbonyl) is decomposed at high temperature and pressure to form CNT, amorphous carbon, and CO_. Each "molecule" of CNT contains roughly 3000 carbon atoms. The reactions by which such molecules are formed are: In the process to be analyzed, a fresh feed of CO saturated with \(\mathrm{Fe}(\mathrm{CO})_{5}(\mathrm{v})\) contains \(19.2 \mathrm{wt} \%\) of the latter component. The feed is joined by a recycle stream of pure CO and fed to the reactor, where all of the iron penta-carbonyl decomposes. Based on laboratory data, \(20.0 \%\) of the CO fed to the reactor is converted, and the selectivity of CNT to amorphous carbon production is (9.00 kmol CNT/kmol C). The reactor effluent passes through a complex separation process that yields three product streams: one consists of solid \(\mathrm{CNT}, \mathrm{C},\) and \(\mathrm{Fe} ;\) a second is \(\mathrm{CO}_{2} ;\) and the third is the recycled \(\mathrm{CO}\). You wish to determine the flow rate of the fresh feed (SCM/h), the total CO_ generated in the process ( \(\mathrm{kg} / \mathrm{h}\) ), and the ratio (kmol CO recycled/kmol CO in fresh feed). (a) Take a basis of \(100 \mathrm{kmol}\) fresh feed. Draw and fully label a process flow chart and do degree-offreedom analyses for the overall process, the fresh-feed/recycle mixing point, the reactor, and the separation process. Base the analyses for reactive systems on atomic balances. (b) Write and solve overall balances, and then scale the process to calculate the flow rate (SCM/h) of fresh feed required to produce \(1000 \mathrm{kg} \mathrm{CNT} / \mathrm{h}\) and the mass flow rate of \(\mathrm{CO}_{2}\) that would be produced. (c) In your degree-of-freedom analysis of the reactor, you might have counted separate balances for C (atomic carbon) and O (atomic oxygen). In fact, those two balances are not independent, so one but not both of them should be counted. Revise your analysis if necessary, and then calculate the ratio (kmol CO recycled/kmol CO in fresh feed). (d) Prove that the atomic carbon and oxygen balances on the reactor are not independent equations.

A paint mixture containing \(25.0 \%\) of a pigment and the balance binders (which help the pigment stick to the surface) and solvents (which ensure that the paint stays in liquid form) sells for 18.00 dollar/kg, and a mixture containing 12.0\% sells for 10.00 dollar /kg. (a) If a paint retailer produces a blend containing \(17.0 \%\) pigment, for how much (S/kg) should it be sold to yield a 10\% profit? (b) Paint manufacturers have begun to market "low VOC" paint as a more environmentally friendly product. What are VOCs? List some ways in which paint products can be altered to lower the VOC content.

A drug (D) is produced in a three-stage extraction from the leaves of a tropical plant. About 1000 kg of leaf is required to produce 1 kg of the drug. The extraction solvent (S) is a mixture containing 16.5 wt\% ethanol (E) and the balance water (W). The following process is carried out to extract the drug and recover the solvent. 1\. A mixing tank is charged with \(3300 \mathrm{kg}\) of \(\mathrm{S}\) and \(620 \mathrm{kg}\) of leaf. The mixer contents are stirred for several hours, during which a portion of the drug contained in the leaf goes into solution. The contents of the mixer are then discharged through a filter. The liquid filtrate, which carries over roughly \(1 \%\) of the leaf fed to the mixer, is pumped to a holding tank, and the solid cake (spent leaf and entrained liquid) is sent to a second mixer. The entrained liquid has the same composition as the filtrate and a mass equal to \(15 \%\) of the mass of liquid charged to the mixer. The extracted drug has a negligible effect on the total mass and volume of the spent leaf and the filtrate. 2\. The second mixer is charged with the spent leaf from the first mixer and with the filtrate from the previous batch in the third mixer. The leaf is extracted for several more hours, and the contents of the mixer are then discharged to a second filter. The filtrate, which contains \(1 \%\) of the leaf fed to the second mixer, is pumped to the same holding tank that received the filtrate from the first mixer, and the solid cake- -spent leaf and entrained liquid - is sent to the third mixer. The entrained liquid mass is \(15 \%\) of the mass of liquid charged to the second mixer. 3\. The third mixer is charged with the spent leaf from the second mixer and with \(2720 \mathrm{kg}\) of solvent \(\mathrm{S}\). The mixer contents are filtered; the filtrate, which contains \(1 \%\) of the leaf fed to the third mixer, is recycled to the second mixer; and the solid cake is discarded. As before, the mass of the entrained liquid in the solid cake is \(15 \%\) of the mass of liquid charged to the mixer. 4\. The contents of the filtrate holding tank are filtered to remove the carried-over spent leaf, and the wet cake is pressed to recover entrained liquid, which is combined with the filtrate. A negligible amount of liquid remains in the wet cake. The filtrate, which contains \(\mathrm{D}, \mathrm{E},\) and \(\mathrm{W},\) is pumped to an extraction unit (another mixer). 5\. In the extraction unit, the alcohol-water-drug solution is contacted with another solvent (F), which is almost but not completely immiscible with ethanol and water. Essentially all of the drug (D) is extracted into the second solvent, from which it is eventually separated by a process of no concern in this problem. Some ethanol but no water is also contained in the extract. The solution from which the drug has been extracted (the raffinate) contains \(13.0 \mathrm{wt} \% \mathrm{E}, 1.5 \% \mathrm{F},\) and \(85.5 \%\) W. It is fed to a stripping column for recovery of the ethanol. 6\. The feeds to the stripping column are the solution just described and steam. The two streams are fed in a ratio such that the overhead product stream from the column contains \(20.0 \mathrm{wt} \% \mathrm{E}\) and \(2.6 \% \mathrm{F},\) and the bottom product stream contains \(1.3 \mathrm{wt} \% \mathrm{E}\) and the balance \(\mathrm{W}\). Draw and label a flowchart of the process, taking as a basis one batch of leaf processed. Then calculate (a) the masses of the components of the filtrate holding tank. (b) the masses of the components \(D\) and \(E\) in the extract stream leaving the extraction unit. (c) the mass of steam fed to the stripping column, and the masses of the column overhead and bottoms products.

Ethane is chlorinated in a continuous reactor: $$\mathrm{C}_{2} \mathrm{H}_{6}+\mathrm{Cl}_{2} \rightarrow \mathrm{C}_{2} \mathrm{H}_{5} \mathrm{Cl}+\mathrm{HCl}$$ Some of the product monochloroethane is further chlorinated in an undesired side reaction: $$\mathrm{C}_{2} \mathrm{H}_{5} \mathrm{Cl}+\mathrm{Cl}_{2} \rightarrow \mathrm{C}_{2} \mathrm{H}_{4} \mathrm{Cl}_{2}+\mathrm{HCl}$$ (a) Suppose your principal objective is to maximize the selectivity of monochloroethane production relative to dichloroethane production. Would you design the reactor for a high or low conversion of ethane? Explain your answer. (Hint: If the reactor contents remained in the reactor long enough for most of the ethane in the feed to be consumed, what would the main product constituent probably be?) What additional processing steps would almost certainly be carried out to make the process economically sound? (b) Take a basis of \(100 \mathrm{mol} \mathrm{C}_{2} \mathrm{H}_{5} \mathrm{Cl}\) produced. Assume that the feed contains only ethane and chlorine and that all of the chlorine is consumed, and carry out a degree-of-freedom analysis based on atomic species balances. (c) The reactor is designed to yield a \(15 \%\) conversion of ethane and a selectivity of \(14 \mathrm{mol} \mathrm{C}_{2} \mathrm{H}_{5} \mathrm{Cl} / \mathrm{mol}\) \(\mathrm{C}_{2} \mathrm{H}_{4} \mathrm{Cl}_{2},\) with a negligible amount of chlorine in the product gas. Calculate the feed ratio \(\left(\mathrm{mol} \mathrm{Cl}_{2} /\right.\) mol \(\mathrm{C}_{2} \mathrm{H}_{6}\) ) and the fractional yield of monochloroethane. (d) Suppose the reactor is built and started up and the conversion is only \(14 \% .\) Chromatographic analysis shows that there is no \(\mathrm{Cl}_{2}\) in the product but another species with a molecular weight higher than that of dichloroethane is present. Offer a likely explanation for these results.

A liquid mixture contains \(60.0 \mathrm{wt} \%\) ethanol \((\mathrm{E}), 5.0 \mathrm{wt} \%\) of a dissolved solute \((\mathrm{S}),\) and the balance water. A stream of this mixture is fed to a continuous distillation column operating at steady state. Product streams emerge at the top and bottom of the column. The column design calls for the product streams to have equal mass flow rates and for the top stream to contain 90.0 wt\% ethanol and no S. (a) Assume a basis of calculation, draw and fully label a process flowchart, do the degree-of-freedom analysis, and verify that all unknown stream flows and compositions can be calculated. (Don't do any calculations yet.) (b) Calculate (i) the mass fraction of \(S\) in the bottom stream and (ii) the fraction of the ethanol in the feed that leaves in the bottom product stream (i.e., \(\mathrm{kg} \mathrm{E}\) in bottom stream/kg \(\mathrm{E}\) in feed) if the process operates as designed. (c) An analyzer is available to determine the composition of ethanol-water mixtures. The calibration curve for the analyzer is a straight line on a plot on logarithmic axes of mass fraction of ethanol, \(x\) (kg E/kg mixture), versus analyzer reading, \(R\). The line passes through the points \((R=15, x=\) 0.100) and \((R=38, x=0.400)\). Derive an expression for \(x\) as a function of \(R(x=\cdots\) ) based on the calibration, and use it to determine the value of \(R\) that should be obtained if the top product stream from the distillation column is analyzed. (d) Suppose a sample of the top stream is taken and analyzed and the reading obtained is not the one calculated in Part (c). Assume that the calculation in Part (c) is correct and that the plant operator followed the correct procedure in doing the analysis. Give five significantly different possible causes for the deviation between \(R_{\text {measured and }} R_{\text {prediced }}\), including several assumptions made when writing the balances of Part (c). For each one, suggest something that the operator could do to check whether it is in fact the problem.

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