Question 4 of 9: N₂/CO₂ Ideal-Gas Mixture, Isentropic Compression
Nivaar worked solution (AI-drafted; not reviewed by a licensed engineer)
Notes on this paper
National Exam 04-BS-10, Thermodynamics — December 2017. 3 hours, Closed-Book Exam (approved
calculator and one double-sided 8.5x11-inch aid sheet permitted; property tables and charts supplied
in an appendix, interpolation not required). Part A: answer 2 of Questions 1-3 (20 marks each). Part
B: answer 4 of Questions 4-9 (15 marks each), for a 100-mark paper. Only the first two Part-A and
first four Part-B questions as they appear in the answer book are marked. All nine questions (Part A
complete, Part B complete) are solved below for completeness.
Reference texts: Cengel & Boles, Thermodynamics: An Engineering
Approach, 8th ed.; Moran, Shapiro, Boettner & Bailey, Fundamentals of Engineering
Thermodynamics, 8th ed. All state properties (water/steam, R-134a, air, N₂, CO₂,
H₂) were computed from high-accuracy equations of state in place of printed property-table interpolation; every boxed numeric result.
Find. Work input per unit mass of mixture, $w_{in}$ [kJ/kg].
Approach
Because the mixture is only 2 components at fixed mole fractions, the molar entropy change of the
mixture on compression is the mole-fraction-weighted sum of each species' own molar entropy change
(Gibbs' theorem for ideal-gas mixtures: each component behaves as if it alone occupied the container
at its own partial pressure, and the $R\ln(y_i)$ mixing terms cancel identically between the inlet and
outlet states since composition doesn't change). Root-solve the isentropic condition for $T_2$ using
each species' variable-cp (temperature-dependent) molar entropy function, then get the molar
enthalpy change the same way and convert to a per-unit-mass mixture result via the mixture's molar
mass.
Isentropic condition ⇒ exit temperature. Composition is unchanged across
the compressor, so the mixing entropy terms cancel and the isentropic condition reduces to
$$y_{N_2}\big[\bar s^\circ_{N_2}(T_2)-\bar s^\circ_{N_2}(T_1)\big]+y_{CO_2}\big[\bar
s^\circ_{CO_2}(T_2)-\bar s^\circ_{CO_2}(T_1)\big]=R_u\ln\frac{P_2}{P_1}.$$
Right-hand side: $R_u\ln(500/100)=8.314\times1.6094=13.381$ kJ/(kmol·K). Root-solving
(both species' molar entropy evaluated via high-accuracy ideal-gas-limit properties) gives
$$\boxed{T_2=881.29\ \text{K}}.$$
Work input per unit mass of mixture. Steady-flow, negligible ΔKE/PE:
$w_{in}=\Delta h_{mix}$ (per unit mass). Mole-weighted molar enthalpy change, divided by $M_{mix}$:
$$\Delta \bar h_{mix}=y_{N_2}\Delta\bar h_{N_2}+y_{CO_2}\Delta\bar h_{CO_2}=0.80\times8731+0.20\times14{,}143=6985+2829=9813\ \text{kJ/kmol}.$$
$$w_{in}=\frac{\Delta\bar h_{mix}}{M_{mix}}=\frac{9813}{31.212}=\boxed{314.41\ \text{kJ/kg}}.$$