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A device is being designed to separate into components a natural gas consisting of \(\mathrm{CH}_{4}\) and \(\mathrm{C}_{2} \mathrm{H}_{6}\) in which the mole fraction of \(\mathrm{C}_{2} \mathrm{H}_{6}\), denoted by \(y\), may vary from \(0.05\) to \(0.50\). The device will receive natural gas at \(20^{\circ} \mathrm{C}, 1 \mathrm{~atm}\) with a volumetric flow rate of \(100 \mathrm{~m}^{3} / \mathrm{s}\). Separate streams of \(\mathrm{CH}_{4}\) and \(\mathrm{C}_{2} \mathrm{H}_{6}\) will exit, each at \(20^{\circ} \mathrm{C}, 1 \mathrm{~atm}\). Heat transfer between the device and its surroundings occurs at \(20^{\circ} \mathrm{C}\). Ignoring kinetic and potential energy effects, plot versus \(y\) the minimum theoretical work input required at steady state, in \(\mathrm{kW}\).

Short Answer

Expert verified
Calculate a series of theoretical work values at different mole fractions, then plot work against the mole fraction of \( \text{C}_2\text{H}_6 \).

Step by step solution

01

Understand the Initial and Final States

Identify the initial and final states of the gas mixture. The natural gas initially contains \( \text{CH}_4 \), methane, and \( \text{C}_2 \text{H}_6 \), ethane, with a varying mole fraction \( y \) of \( \text{C}_2 \text{H}_6 \) from 0.05 to 0.50. The device separates these gases at constant temperature and pressure (20°C, 1 atm).
02

Calculate Molar Flow Rate (Inlet)

Use the ideal gas law to determine the molar flow rate of the incoming gas.The volumetric flow rate is 100 m³/s at 20°C and 1 atm.Use the ideal gas law \( PV = nRT \) to find the molar flow rate \( \text{n}_{\text{in}} \):\[ n_{\text{in}} = \frac{100 \text{m}^3/\text{s} \times 1 \text{atm}}{0.0821 \text{ (L·atm)/(K·mol) } \times (273 + 20) \text{K}} \]Calculate n_in:
03

Calculate the Molar Flow Rates of Components at the Outlet

Based on the mole fraction y, the molar flow rates for \( \text{CH}_4 \) and \( \text{C}_2 \text{H}_6 \) at the outlet can be determined:\( \text{n}_{\text{C}_2\text{H}_6} = y \times n_{\text{in}} \)\( \text{n}_{\text{CH}_4} = (1 - y) \times n_{\text{in}} \)
04

Determine the Entropy Changes

Calculate the entropy change for each component assuming ideal gas behavior and isothermal process.For \( \text{CH}_4 \):\[ \text{ΔS}_{\text{CH}_4} = \text{n}_{\text{CH}_4} R \text{ln} \frac{n_{\text{CH}_4}}{n_{\text{in}}} \]For \( \text{C}_2 \text{H}_6 \):\[ \text{ΔS}_{\text{C}_2\text{H}_6} = \text{n}_{\text{C}_2\text{H}_6} R \text{ln} \frac{n_{\text{C}_2\text{H}_6}}{n_{\text{in}}} \]
05

System Entropy Change

Sum the entropy changes to find the total change in entropy of the system.\[ \text{ΔS}_{\text{total}} = \text{ΔS}_{\text{CH}_4} + \text{ΔS}_{\text{C}_2\text{H}_6} \]
06

Calculate Minimum Theoretical Work

Use the total entropy change to find the minimum theoretical work input using Gibbs free energy relation:\[ \text{W}_{\text{min}} = -T \text{ΔS}_{\text{total}} \]Where \( T \) is the temperature in Kelvin (293 K).
07

Plot Work vs. Mole Fraction y

Vary \( y \) from 0.05 to 0.50 and calculate \( \text{W}_{\text{min}} \) for each value of \( y \). Plot these values to visualize how the minimum theoretical work input changes with the mole fraction of \( \text{C}_2 \text{H}_6 \).

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Key Concepts

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

thermodynamics
In thermodynamics, we study the energy interactions that occur in a system. For the separation of natural gas into \(\text{CH}_4\) (methane) and \(\text{C}_2\text{H}_6\) (ethane), we harness principles of thermodynamics to understand and calculate the energy changes involved. Specifically, we focus on variables like temperature, pressure, and volume, which are paramount in determining energy changes. By analyzing these transformations, we can be more efficient in designing processes like gas separation. The principles of thermodynamics help us ensure that we are moving energy in the most efficient way possible, minimizing wasted energy and allowing us to calculate the minimum work required for the process.
ideal gas law
The ideal gas law is a cornerstone in the realm of thermodynamics. It links pressure (\text{\text{P}}), volume (\text{\text{V}}), temperature (\text{\text{T}}), and the amount of gas (\text{\text{n}}) using the equation: \[ PV = nRT \] where \(R\) is the universal gas constant (\text{0.0821 L·atm/(K·mol)}). In this particular problem, the natural gas mixture at the inlet has a volumetric flow rate of \text{100 m³/s} at \text{20°C} and \text{1 atm}. By converting the temperature to Kelvin (\text{273 K + 20°C}), and plugging in the values on the right side of the ideal gas equation, we can solve for the molar flow rate (\text{N_in}). This step is critical as it allows us to understand the amount of gas we are handling in the system, setting up for the calculation of downstream component flows.
entropy change
Entropy, denoted as \( S \), brings the concept of disorder to thermodynamics. In gas separation processes, we encounter entropy change due to mixing and separating gases. For ideal gases undergoing isothermal processes (constant temperature), the entropy change can be given by the formula: \[ \text{ΔS} = nR \text{ln}\frac{V_2}{V_1} \]For our problem, since we are dealing with molar flow rates, this translates to: \[ \text{ΔS}_{\text{component}} = n_{component} R \text{ln} \frac{n_{component}}{n_{\text{in}}} \] We need to calculate the entropy change separately for \text{CH}_4 and \text{C}_2\text{H}_6. Summing these gives the total entropy change of the system. Understanding entropy change helps quantify the energy dispersal in the separation process, impacting the theoretical work required.
molar flow rate
Molar flow rate is a key aspect when dealing with chemical processes like gas separation. It refers to the quantity of a component flowing per unit time, usually expressed in \text{mol/s}. In this context, we need to determine the molar flow rate of the incoming natural gas mixture. Utilizing the ideal gas law, we found \text{n}_{\text{in}}, the total molar flow rate of the mixture. The device then separates this stream into \text{CH}_4 and \text{C}_2\text{H}_6} based on their mole fractions (\text{y}). We calculate the molar flow rates of individual components as: \[n_{\text{C}_2\text{H}_6} = y \times n_{\text{in}} \] \[n_{\text{CH}_4} = (1 - y) \times n_{\text{in}} \]This information is pivotal as it feeds into further calculations including entropy change and theoretical work.
theoretical work
Theoretical work is a measure of the minimum energy required to achieve a process, calculated under ideal conditions with no losses. For the given problem, the work input needed for the gas separation device can be determined using the total entropy change calculated earlier. The relationship between work and entropy is given by: \[ \text{W}_{\text{min}} = -T \text{ΔS}_{\text{total}} \] Where \text{T} is the temperature in Kelvin. This gives a measure of the minimal energy input to drive the separation process at a steady state. By varying the mole fraction \text{y} from \text{0.05} to \text{0.50} and calculating \text{W}_{\text{min}} for each \text{y}, we can understand how the minimum theoretical work changes with the composition of the natural gas.

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Most popular questions from this chapter

Helium at \(400 \mathrm{~K}, 1\) bar enters an insulated mixing chamber operating at steady state, where it mixes with argon entering at \(300 \mathrm{~K}, 1\) bar. The mixture exits at a pressure of \(1 \mathrm{bar}\). If the argon mass flow rate is \(x\) times that of helium, plot versus \(x\) (a) the exit temperature, in \(\mathrm{K}\). (b) the rate of exergy destruction within the chamber, in \(\mathrm{kJ}\) per \(\mathrm{kg}\) of helium entering. Kinetic and potential energy effects can be ignored. Let \(T_{0}=\) \(300 \mathrm{~K}\).

Atmospheric air having dry-bulb and wet-bulb temperatures of 33 and \(29^{\circ} \mathrm{C}\), respectively, enters a well-insulated chamber operating at steady state and mixes with air entering with dry-bulb and wet- bulb temperatures of 16 and \(12^{\circ} \mathrm{C}\), respectively. The volumetric flow rate of the lower temperature stream is three times that of the other stream. A single mixed stream exits. The pressure is constant throughout at 1 atm. Neglecting kinetic and potential energy effects, determine for the exiting stream (a) the relative humidity. (b) the temperature, in \({ }^{\circ} \mathrm{C}\).

Answer the following questions involving a mixture of two gases: (a) When would the analysis of the mixture in terms of mass fractions be identical to the analysis in terms of mole fractions? (b) When would the apparent molecular weight of the mixture equal the average of the molecular weights of the two gases?

Air at \(77^{\circ} \mathrm{C}, 1\) bar, and a molar flow rate of \(0.1 \mathrm{kmol} / \mathrm{s}\) enters an insulated mixing chamber operating at steady state and mixes with water vapor entering at \(277^{\circ} \mathrm{C}, 1\) bar, and a molar flow rate of \(0.3 \mathrm{kmol} / \mathrm{s}\). The mixture exits at 1 bar. Kinetic and potential energy effects can be ignored. For the chamber, determine (a) the temperature of the exiting mixture, in \({ }^{\circ} \mathrm{C}\). (b) the rate of entropy production, in \(\mathrm{kW} / \mathrm{K}\).

A control volume operating at steady state has two entering streams and a single exiting stream. A mixture with a mass flow rate of \(11.67 \mathrm{~kg} / \mathrm{min}\) and a molar analysis \(9 \% \mathrm{CH}_{4}\), \(91 \%\) air enters at one location and is diluted by a separate stream of air entering at another location. The molar analysis of the air is \(21 \% \mathrm{O}_{2}, 79 \% \mathrm{~N}_{2}\). If the mole fraction of \(\mathrm{CH}_{4}\) in the exiting stream is required to be \(5 \%\), determine (a) the molar flow rate of the entering air, in \(\mathrm{kmol} / \mathrm{min}\). (b) the mass flow rate of oxygen in the exiting stream, in \(\mathrm{kg} / \mathrm{min} .\)

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