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Modern Engineering Thermodynamics

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240 CHAPTER 7: Second Law of <strong>Thermodynamics</strong> and Entropy Transport and Production Mechanisms<br />

a vaporization process), Q rev > Q act . The irreversibilities involved in a phase change process arise largely from the<br />

heat transfer required to produce the phase change and from the mechanical moving boundary work associated<br />

with any volume change between the phases. If the real system is truly isothermal, then heat transfer irreversibilities<br />

may be allocated to the system’s surroundings. As for the work mode irreversibilities, for a reversible<br />

process, ðdWÞ rev<br />

= −mp dv, and the differential energy balance then gives ðdQÞ rev<br />

= mdu+ ð pdvÞ = mdh ð Þ.However,<br />

for an actual irreversible process ðdWÞ act = f ðη W ÞðdWÞ rev ,wheref(η W ) is a function of the work transport<br />

energy efficiency, given in Eqs. (4.71) and (4.72), immediately preceding Eq. (7.46). Then, ðdQÞ act =<br />

m½du + f ðη W ÞpdvŠ ≠ mdh ð Þ. Consequently, if there is negligible change in system volume during the phase change<br />

or the moving boundary work is carried out very efficiently, then the work mode irreversibilities also are insignificant.<br />

Under these conditions, the actual phase change can be accurately approximated as a reversible<br />

process.<br />

7.17 ENTROPY BALANCE AND ENTROPY RATE BALANCE<br />

EQUATIONS<br />

The resulting entropy balance for a closed system of mass m is given by integrating Eq. (7.48) and substituting<br />

in Eqs. (7.60), (7.62), (7.65), and (7.69) to produce<br />

Z<br />

τ<br />

General closed system entropy balance ðSBÞ<br />

Z <br />

_q<br />

dA dt + 1 ðS P Þ<br />

Σ T 2 = ðS 2 − S 1 Þ system =½mðs 2 − s 1 ÞŠ system (7.75)<br />

b act<br />

For the simplified case of isothermal boundaries, this equation reduces to<br />

where in each case<br />

Isothermal boundary closed system entropy balance<br />

<br />

1Q 2<br />

+ 1 ðS P Þ<br />

T 2<br />

= ms ð 2 − s 1 Þ (7.76)<br />

b act<br />

Z Z<br />

1ðS P Þ 2 =<br />

τ V<br />

<br />

− _q <br />

dT<br />

T 2 + σ W<br />

dx<br />

<br />

dV dt<br />

In Chapter 9, Eq. (7.75) is expanded into the following open system general entropy rate balance equations.<br />

General open system entropy rate balance ðSRBÞ<br />

Z <br />

_q<br />

dA +∑ _ms − ∑ _ms + _S P = _S system (9.4)<br />

Σ T b act inlet outlet<br />

and, for the simplified case of isothermal boundaries, this equation reduces to<br />

Isothermal boundary open system entropy rate balance<br />

<br />

_Q<br />

_ms −∑ _ms + _S p = _S system (9.5)<br />

T b act<br />

out<br />

+∑<br />

in<br />

There are two effective ways for calculating the entropy production or the entropy production rate for any<br />

process: the direct and the indirect methods.<br />

■<br />

Direct method involves calculating the amount of entropy produced for a process from its defining<br />

equations. For example, for closed systems, the direct method of calculating the entropy production rate is<br />

Z<br />

_S P = ðσ Q + σ W ÞdV<br />

V<br />

where<br />

<br />

σ Q = _q <br />

dT<br />

T 2 dx<br />

actual<br />

and<br />

σ W = σ viscous + σ electrical + ⋯

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