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Modern Engineering Thermodynamics

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Summary 273<br />

Note that this example does not include the entropy production due to the heat transfer required to cool the mixture down<br />

to a drinkable temperature.<br />

Exercises<br />

29. Recalculate the entropy production in Example 8.15 when the average specific heat of the mixture of coffee and cream of<br />

3856 J/(kg·K) is used instead of the value for pure water. Keep the values of all the other variables the same as they are<br />

in Example 8.15. Answer: 1 (S P ) 2 = 0.259 J/K.<br />

30. Determine the entropy production in the mixing process described in Example 8.15 when the temperature of the cream is<br />

20.0°C and the temperature of the coffee is 90.0°C. Keep the vales of all the other variables the same as they are in<br />

Example 8.15. Answer: 1 (S P ) 2 = 0.265 J/K.<br />

31. (a) Determine the entropy produced in the process described in Example 8.15 when the mass of the cream added is<br />

increased from 3.00 g to 10.0 g. Keep the values of all the other variables the same as they are in Example 8.15. (b) Plot<br />

1(S P ) 2 /(m a + m b ) vs. the mass fraction y over the range 0 ≤ y ≤ 1 for the values of c, T a , and T b used in Example 8.15.<br />

(c) What value of y maximizes 1 (S P ) 2 in part b? Answers: (a) 1 (S P ) 2 = 0.911 J/K, (b) See Figure 8.20, (c) [ 1 (S P ) 2 ] max<br />

occurs at y = 0.52.<br />

Coffee entropy production per unit mass<br />

of mixture, J/kg.K<br />

30<br />

24<br />

18<br />

12<br />

6<br />

0<br />

0.0<br />

0.2 0.4 0.6 0.8 1.0<br />

y = m a /(m a + m b )<br />

FIGURE 8.20<br />

Example 8.15, Exercise 31, part b.<br />

Equations (8.12) and (8.13) show that the amount of entropy production in this type of mixing process<br />

depends on the amounts mixed and their initial states. The larger the property differences between the initial<br />

states, the larger is entropy production on mixing. That is, the farther the initial states are from the final equilibrium<br />

state, the larger the associated entropy production is. This is a general characteristic of the second law.<br />

SUMMARY<br />

In this chapter, the energy and entropy balance and rate balance equations are used to investigate various<br />

closed system applications. The indirect method of calculating values for S P and _S P occurs when they are calculated<br />

from the entropy balance or the entropy rate balance equations. But, when these values are calculated<br />

from the applicable entropy production rate density equations (σ W ) defined in Chapter 7, we called this the<br />

direct method.<br />

Reversible processes are defined as processes that occur with no internal irreversibilities, such as friction, viscosity,<br />

heat transfer, or diffusion. Then, S P and _S P = 0, and the closed system entropy balance and entropy rate<br />

balance equations for a reversible process reduce to<br />

<br />

Entropy balance ðSBÞ: S 2 − S 1 = ms ð 2 − s 1 Þ = 1 Q 2<br />

(8.7)<br />

T b<br />

and<br />

<br />

Q<br />

Entropy rate balance ðSRBÞ: _S = m_s =<br />

_ <br />

T b<br />

rev<br />

rev<br />

(8.8)

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