EBK INTRODUCTION TO CHEMICAL ENGINEERIN
EBK INTRODUCTION TO CHEMICAL ENGINEERIN
8th Edition
ISBN: 9781259878091
Author: SMITH
Publisher: MCGRAW HILL BOOK COMPANY
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Chapter 6, Problem 6.26P
Interpretation Introduction

Interpretation:

The temperature of steam in its final state along with the change in entropy should be deduced based on steam table data as well as based on the ideal gas assumption.

Concept Introduction:

  • For a two-phase liquid-vapor equilibrium mixture the specific volume (V), enthalpy (H) and entropy (S) are given as:

V = Vf + x(Vg-Vf) -----(1)H = Hf + x(Hg-Hf)-----(2)S = Sf + x(Sg-Sf)--------(3)where, Vg and Vf are the specific volumes in the vapor and liquid phases respectively Hg and Hf are the specific enthalpies in the vapor and liquid phases respectivelySg and Sf are the specific entropies in the vapor and liquid phases respectivelyx = steam quality 

  • For a process that takes place at constant enthalpy, the change in enthalpy is zero. In other words, the enthalpy in the final state (H2) is equal to that in the initial state (H1). The change in enthalpy is given as:

ΔH = H2-H1 -----(4)When, ΔH = 0 H2 = H1 

Based on steam tables:

The final temperature of steam, T = 225C0

The entropy change, ?S = 1.2685 kJ/kg-K

Based on the ideal gas assumption:

The final temperature of steam, T = 260C0

The entropy change, ?S = 1.3032 kJ/kg-K

Given:

Initial pressure of steam, P1 = 300 psi

Initial Temperature of steam = 500F0

Final pressure P2 = 20 psi

Explanation:

Since this is a constant enthalpy process, H1 = H2

The initial state enthalpy (H1) and entropy (S1) can be deduced based on the steam table data for superheated steam at 300 psi.

The final state temperature and entropy (S2) can be deduced from steam tables from the calculated initial enthalpy data.

Calculations:

Step 1:

Calculate the initial state enthalpy (H1) and entropy (S1) at T = 500F0

Based on the steam tables at the initial state pressure = 300 psi we have:

For superheated steam:

At Saturation temperature, T = 500F0

Specific enthalpy of vapor, Hg = H1 = 1257.7 Btu/lbm

Specific entropy of vapor, Sg = S1= 1.5703 Btu/lbm-K

Step 2:

Calculate the final temperature and ?S

Since, H2 = H1 We have, H2 = 1257.7 Btu/lbm

Based on the steam tables the above specific enthalpy final temperature can be deduced from superheated steam table data by interpolation:

For a final pressure P2 = 30 psi

At Saturation temperature, T = 400F0 ; Specific enthalpy of vapor, Hg = 1237.8 Btu/lbm

At Saturation temperature, T = 450F0 ; Specific enthalpy of vapor, Hg = 1261.9 Btu/lbm

Thus, the final temperature can be calculated from interpolation based on the above data:

  T2 = 400 + 1257.7-1237.81261.9-1237.8(450-400)= 441.3F0

At Saturation temperature, T = 400F0 ; Specific entropy of vapor, Sg = 1.7937 Btu/lbm-K

At Saturation temperature, T = 450F0 ; Specific entropy of vapor, Sg = 1.8210 Btu/lbm-K

Thus, the final entropy can be calculated from interpolation based on the above data:

  S2 = 1.7937 + 441-400450-400(1.8120-1.7937)= 1.8087 Btu/lbm-K

Thus, the final state temperature, T2 = 441F0

Specific entropy of vapor at this final temperature, S2 = 1.8087 Btu/lbm-K

ΔS = S2- S1 = 1.8087 - 1.5703 = 0.2384 Btu/lbm-K

Step 3:

Calculate the final temperature and ?S based on the ideal gas assumption

Enthalpy is a state function and dependent on temperature. Since the process takes place at constant enthalpy, there is will be no change in temperature.

T2 = T1 = 500F0

The entropy change for an ideal gas is:

ΔS = CvlnT2T1 + RlnP2P1Since T2 = T1ΔS = RlnP2P1=0.008314 kJ .K -1 .mol -10.018 kg .mol -1×ln20300=1.2508 Btu/lbm-K

Thus,

Based on steam tables:

The final temperature of steam, T = 441F0

The entropy change, ?S = 0.2384 kJ/kg-K

Based on the ideal gas assumption:

The final temperature of steam, T = 500F0

The entropy change, ?S = 1.2508 kJ/kg-K

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Chapter 6 Solutions

EBK INTRODUCTION TO CHEMICAL ENGINEERIN

Ch. 6 - Prob. 6.11PCh. 6 - Prob. 6.12PCh. 6 - Prob. 6.13PCh. 6 - Prob. 6.14PCh. 6 - Prob. 6.15PCh. 6 - Prob. 6.16PCh. 6 - Prob. 6.17PCh. 6 - Prob. 6.18PCh. 6 - Prob. 6.19PCh. 6 - Prob. 6.20PCh. 6 - Prob. 6.21PCh. 6 - Prob. 6.22PCh. 6 - Prob. 6.23PCh. 6 - Prob. 6.24PCh. 6 - Prob. 6.25PCh. 6 - Prob. 6.26PCh. 6 - Prob. 6.27PCh. 6 - What is the mole fraction of water vapor in air...Ch. 6 - Prob. 6.29PCh. 6 - Prob. 6.30PCh. 6 - Prob. 6.31PCh. 6 - Prob. 6.32PCh. 6 - Prob. 6.33PCh. 6 - Prob. 6.34PCh. 6 - Prob. 6.35PCh. 6 - Prob. 6.36PCh. 6 - Prob. 6.37PCh. 6 - Prob. 6.38PCh. 6 - Prob. 6.39PCh. 6 - Prob. 6.40PCh. 6 - Prob. 6.41PCh. 6 - Prob. 6.42PCh. 6 - Prob. 6.43PCh. 6 - Prob. 6.44PCh. 6 - Prob. 6.45PCh. 6 - Prob. 6.46PCh. 6 - Prob. 6.47PCh. 6 - Prob. 6.48PCh. 6 - Prob. 6.49PCh. 6 - Prob. 6.50PCh. 6 - Prob. 6.51PCh. 6 - Prob. 6.52PCh. 6 - Prob. 6.53PCh. 6 - Prob. 6.54PCh. 6 - Prob. 6.55PCh. 6 - Prob. 6.56PCh. 6 - Prob. 6.57PCh. 6 - Prob. 6.58PCh. 6 - Prob. 6.59PCh. 6 - Prob. 6.60PCh. 6 - Prob. 6.61PCh. 6 - Prob. 6.62PCh. 6 - Prob. 6.63PCh. 6 - Prob. 6.64PCh. 6 - Prob. 6.65PCh. 6 - Prob. 6.66PCh. 6 - Prob. 6.67PCh. 6 - Prob. 6.68PCh. 6 - Prob. 6.69PCh. 6 - Prob. 6.71PCh. 6 - Prob. 6.72PCh. 6 - Prob. 6.73PCh. 6 - Prob. 6.74PCh. 6 - Prob. 6.75PCh. 6 - Prob. 6.76PCh. 6 - Prob. 6.77PCh. 6 - Prob. 6.78PCh. 6 - Prob. 6.79PCh. 6 - Prob. 6.80PCh. 6 - Prob. 6.81PCh. 6 - The temperature dependence of the second virial...Ch. 6 - Prob. 6.83PCh. 6 - Prob. 6.84PCh. 6 - Prob. 6.85PCh. 6 - Prob. 6.86PCh. 6 - Prob. 6.87PCh. 6 - Prob. 6.88PCh. 6 - Prob. 6.89PCh. 6 - Prob. 6.90PCh. 6 - Prob. 6.91PCh. 6 - Prob. 6.92PCh. 6 - Prob. 6.93PCh. 6 - Prob. 6.94PCh. 6 - Prob. 6.95PCh. 6 - Prob. 6.96PCh. 6 - Prob. 6.97PCh. 6 - Prob. 6.98PCh. 6 - Prob. 6.99PCh. 6 - Prob. 6.100P
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