TABLE 4-2 States and Values of Properties for the Process of Fig.

4-12*
Point P (bar) T (K) Composition State H (J/mol) S (J/mol/K) Flow (mol) Exergy (J/mol) Exergy (J) Point
1 55.22 300 Air Superheated 12,046 82.98 1 -12848 -12848 1
2 1.01 295 Pure O2 Superheated 13,460 118.48 0.1364 -22084 -3012 2
3 1.01 295 91.48% N2 Superheated 12,074 114.34 0.8636 -22228 -19196 3
4 55.22 147.2 Air Superheated 5,850 52.08 1 -9774 -9774 4
5 1.01 79.4 91.48% N2 Saturated vapor 5,773 75.82 0.8636 -16973 -14658 5
6 1.01 90 pure O2 Saturated vapor 7,485 83.69 0.1364 -17622 -2404 6
7 1.01 300 Air Superheated 12,407 117.35 1 -22798 -22798 7
*Properties on the basis of Miller and Sullivan, U.S. Bur. Mines Tech. Pap. 424 (1928).
T (K) 300
Comp stage 3
Comp isentropic eff 80%
Compressor J 15171 Compressor power
E means exergy, number means Point. Not mean excel cell reference
Ideal work J 590 3.9% = E2 + E3 - E7
Compressor loss J 5221 34.4% = Compressor power - (E1 - E7)
Exchanger loss J 2073 13.7% = E1 + E5 + E6 - E2 - E3 - E4
Column loss J 7288 48.0% = E4 - E5 - E6
15171 100.0%
Note: You can find this calculation in Perry's Chemical Engineers' Handbook (7th edition, Chapter 4 Thermodynamics, Page 4-36)
In the Perry's calculation, Exergy lost = T * S
While in my calculation, Exergy lost = Exergy in - Exergy out. It's easiler to understand and the calculations is also faster.
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