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Modern Engineering Thermodynamics

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Problems 403<br />

Design Problems<br />

The following are open-ended design problems. The objective is to<br />

carry out a preliminary thermal design as indicated. A detailed design<br />

with working drawings is not expected unless otherwise specified.<br />

These problems do not have specific answers, so each student’s<br />

design is unique.<br />

70. Design a system to liquefy nitrogen by repeatedly expanding it<br />

until it reaches the saturation temperature. (Hint: Consult your<br />

library about the Linde gas liquefaction process.)<br />

71. Design a system to cut ice into various two-dimensional shapes<br />

using localized pressure to produce a phase change and thus<br />

locally “melting” out the desired shape. (Suggestion: Try a highpressure<br />

“cookie-cutter” technique.)<br />

72.* Design a fire extinguisher system that expands liquid carbon<br />

dioxide under a suitable pressure at ambient temperature<br />

(which can vary by ±50.0°C) and produce a fine spray of solid<br />

carbon dioxide particles at high velocity and low temperature.<br />

73. Design a 3.00 ft 3 cylindrical tank that safely contains oxygen gas<br />

at 2500. psia under ambient temperature conditions (which can<br />

vary by ±100.°F). (Suggestion: Consult the ASME Pressure<br />

Vessel Design Codes in your library.)<br />

74.* Design an experiment that illustrates and accurately measures<br />

the difference in p-v-T behavior between water vapor and a<br />

suitable ideal gas (such as air) over the temperature range from<br />

0.00 to 150.°C.<br />

Computer Problems<br />

The following computer assignments are designed to be carried out<br />

on a personal computer using a spreadsheet or equation solver. They<br />

may be used as part of a weekly homework assignment.<br />

75.* Develop a computer program, spreadsheet, equation solver, or<br />

the like to determine the percent error in the pressure predicted<br />

by the van der Waals equation of state for water along the T =<br />

500°C isotherm, p = RT/(v – b) – a/v 2 . Use Table C.3b or other<br />

appropriate tables for the actual values of p for various values of<br />

v at T = 500.°C. The van der Waals coefficients for water vapor<br />

can be found in Table C.15b.<br />

76.* Develop a computer program, spreadsheet, equation solver, or<br />

the like to determine the percent error in the pressure predicted<br />

by the Beattie-Bridgeman equation of state for water along the<br />

T = 500.°C isotherm, p = [(1 – ε)(v + B)RT – A]/v 2 , where<br />

A =A o (1 – a/v), B = B o (1 – b/v), and ε = c/(vT 3 ). Use Table C.3b<br />

or other appropriate tables for the actual values of p for various<br />

values of v at T = 500.°C. The Beattie-Bridgeman coefficients for<br />

water vapor can be found in Table C.15b.<br />

77.* Develop a computer program, spreadsheet, equation solver, or the<br />

like to determine the percent error in the pressure predicted by the<br />

Redlich-Kwong equation of state for water along the T =500.°C<br />

isotherm, p = RT/(v – b) – a/[v (v + b)T 1/2 ]. Use Table C.3b or other<br />

appropriate tables for the actual values of p for various values of v<br />

at T =500.°C. The Redlich-Kwong coefficients for water vapor can<br />

be found in Table C.15b.<br />

78. Plot a minimum of 100 points along the T = 500. R isotherm<br />

on p-v coordinates for air using<br />

a. The ideal gas equation of state.<br />

b. The Clausius equation of state (use the van der Waals value<br />

for b).<br />

79. Plot a minimum of 100 points along the T = 500. R isotherm<br />

on p-v coordinates for hydrogen using<br />

a. The ideal gas equation of state.<br />

b. The van der Waals equation of state.<br />

80. Plot a minimum of 100 points along the T = 500. R isotherm<br />

on p-v coordinates for methane using<br />

a. The ideal gas equation of state.<br />

b. The Beattie-Bridgeman equation of state.<br />

81. Using the steam tables as a guide, find the regions on a Mollier<br />

diagram or a p-v diagram where the ideal gas equations with<br />

constant specific heats are accurate to within ±1.00% for<br />

a. Specific volume v.<br />

b. Enthalpy h.<br />

c. Entropy s.<br />

82. Expand Problem 81 by adding temperature-dependent ideal gas<br />

specific heats.<br />

83. Expand Problem 81 by using the van der Waals equation of<br />

state in place of the ideal gas equation of state.<br />

84. Develop an interactive computer program for ammonia using<br />

the Beattie-Bridgeman equation of state to produce the<br />

following results from responses to appropriate screen prompts:<br />

a. Output p when v and T are input.<br />

b. Output T when p and v are input.<br />

c. Output v when p and T are input.<br />

85. Develop an interactive computer program that replaces the gas<br />

tables Tables C.16a and C.16b. Do this in two steps:<br />

a. First have the program return u, h, ϕ, p r , and v r when T is<br />

input by assuming constant specific heats.<br />

b. Modify the program developed in step a to include the<br />

temperature-dependent specific heats given in Table C.14<br />

in Thermodynamic Tables to accompany <strong>Modern</strong> <strong>Engineering</strong><br />

<strong>Thermodynamics</strong>.<br />

86.* The purpose of this assignment is to investigate the accuracy of<br />

several historically important p-T relations for saturated water<br />

vapor. Using the tables in the tables book or some other source<br />

for accurate saturation p-T data, calculate, tabulate, and plot the<br />

percent error in saturation pressure for each of the following<br />

cases using % error = (CP – TP)/TP, where CP is the calculated<br />

saturation pressure and TP is the saturation pressure found in<br />

the steam tables.<br />

a. By 1847, Henri Regnault had developed an equation from<br />

his experimental p sat – T sat results for saturated steam. It was<br />

valid in the range of −33.0 to 232°C and had the form<br />

where p sat is in mm Hg and<br />

log 10 p sat = A − BD n − CE n<br />

A = 6:2640348 log 10 D = 9:994049292 − 10<br />

log 10 B = 0:1397743 log 10 E = 9:998343862 − 10<br />

log 10 C = 0:6924351<br />

n = T sat + 20:0°C<br />

Make your % error calculations every 20.0°C between 20.0<br />

and 220.°C.<br />

b. In 1849 Williams Rankine fit his own equation to<br />

Regnault’s data and came up with the following relation:<br />

log 10 p sat = A − B/T sat − C/Tsat<br />

2<br />

where p sat is in psia and T sat = T sat (in °F) + 461.2 (–461.2°F<br />

was Rankine’s best estimate of absolute zero), and<br />

A = 6:1007 log 10 B = 3:43642 log 10 C = 5:59873

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