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Modern Engineering Thermodynamics

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294 CHAPTER 9: Second Law Open System Applications<br />

Similarly, the appropriate entropy rate balance equation for an isothermal system boundary is<br />

_S P<br />

mixing = _m Q<br />

3s 3 − _m 1 s 1 − _m 2 s 2 − _ T b<br />

Q<br />

= _m 3 ½ys ð 2 − s 1 Þ+ ðs 3 − s 2 ÞŠ− _<br />

Many mixing systems use the inlet flow streams to induce mixing and thus tend to be isobaric (i.e., p 1 = p 2 = p 3 ). 4 To<br />

simplify the preceding results somewhat, consider the adiabatic, aergonic, isobaric mixing of two flow streams of the<br />

same material but at different temperatures. Then, these formulae reduce to<br />

and<br />

T b<br />

yh ð 1 − h 2 Þ+ ðh 2 − h 3 Þ = 0 (9.28)<br />

Entropy production rate in mixing two nonreacting flow streams<br />

_S P<br />

mixing = _m 3½ys ð 2 − s 1 Þ+ ðs 3 − s 2 ÞŠ> 0 (9.29)<br />

If these materials are identical incompressible liquids with negligible mixer pressure loss or identical ideal gases<br />

with constant specific heats, then Eqs. (6.19) and (7.33) or Eqs. (6.22) and (7.37) can be used to give<br />

yT ð 1 − T 2 Þ+ T 2 − T 3 = 0 (9.30)<br />

and<br />

<br />

_S P<br />

mixing = _m 3c yln T 2<br />

+ ln T <br />

3<br />

T 1 T 2<br />

(9.31)<br />

where c = c p in the case of ideal gases. Combining these two equations by eliminating T 3 gives<br />

Entropy production rate in mixing two flow streams of the same<br />

incompressible liquid or the same ideal gas in this case, c = c p<br />

<br />

<br />

<br />

_S P<br />

mixing = _m 3c ln 1 + y T <br />

1<br />

− 1<br />

T 2<br />

<br />

−y<br />

T1<br />

T 2<br />

<br />

(9.32)<br />

For a given T 1 /T 2 ratio, there is a critical mass fraction (y c )thatproducesamaximum rate of entropy production. 5 The<br />

critical mass fraction can be found from Eq. (9.32) by setting d _S P /dy = 0andsolvingfory = y c . The result is<br />

which gives<br />

ð<br />

y c = 1 − T 1/T 2 Þ+ lnðT 1 /T 2 Þ<br />

ð1 − T 1 /T 2 ÞlnðT 1 /T 2 Þ<br />

<br />

<br />

<br />

T _S P mixing = _m 3 c ln 1 + y 1<br />

c − 1<br />

ðmaxÞ<br />

T 2<br />

<br />

− yc<br />

T1<br />

T 2<br />

<br />

(9.33)<br />

(9.34)<br />

Figure 9.11 shows the variation in y c with the absolute temperature ratio T 1 /T 2 , and Figure 9.12 shows the<br />

resulting _S P<br />

mixing ðmaxÞ vs. T 1/T 2 relation.<br />

Note that y c is limited by its definition to be less than or equal to 1 in Figure 9.11 and that, in Figure 9.12, it is<br />

impossible to have a mixer whose entropy production rate falls in the region above the curve shown.<br />

Finally, the analysis of the adiabatic, aergonic, isobaric (i.e., viscousless) mixing of identical ideal gases with<br />

constant specific heats produces formulae identical to Eqs. (9.32), (9.33), and (9.34) except c is replaced with<br />

the constant pressure specific heat c p .<br />

4 Isobaric mixing also requires negligible viscous friction losses.<br />

5 It is a maximum because d 2 _ S P /dy 2 < 0 when evaluated at y = y c . Also, the minimum value of _S P is always zero, which occurs here<br />

when T 1 = T 2 .

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