23-Chem-A1 Process Balances and Chemical Thermodynamics · May 2015
Nivaar worked solution (AI-drafted; not reviewed by a licensed engineer)
National Exams — May 2015 — 04-Chem-A1 Process Balances and Chemical Thermodynamics. Three-hour, open-book exam; any non-communicating calculator permitted. Format: seven questions in three parts — answer one of Q1–Q2 (Part A, 15 marks), one of Q3–Q4 (Part B, 25 marks) and two of Q5–Q7 (Part C, 30 marks each); four questions totalling 100 marks constitute a complete paper. All seven are solved below for completeness. Property data (Cp coefficients, steam-table and thermochemical values) are stated explicitly in each Given block.
Reference texts: Felder, Rousseau & Bullard, Elementary Principles of Chemical Processes (4th ed., Wiley) — material & energy balances, humidity, phase equilibria and reactive systems; Smith, Van Ness, Abbott & Swihart, Introduction to Chemical Engineering Thermodynamics (8th ed., McGraw-Hill) — excess Gibbs energy, VLE, activity-coefficient models and reaction equilibrium; supporting data from the NIST/ASME steam tables, Perry's Chemical Engineers' Handbook (9th ed.) and the NIST Chemistry WebBook.
Question text not reproduced: the examination questions are © Engineers and Geoscientists BC. Open the official past paper (linked at the top of this page) to read the question, then follow the worked solution below.
Given. Feed 100 mol/s (75 N₂ + 25 H₂O) at 300 °C, 2 bar. First contactor at 2 bar; gas leaves saturated at 40 °C. Interstage compressor to 6 bar, 200 °C. Second contactor at 6 bar; gas leaves saturated at 25 °C. Liquid water fed to each contactor enters at 20 °C. $M_{\text{H}_2\text{O}}=0.01802$ kg/mol. N₂ enthalpies (kJ/mol, ref 25 °C): $\hat H(300)=8.12$, $\hat H(200)=5.13$, $\hat H(40)=0.438$, $\hat H(25)=0$.
Find. (a) $\hat H$ of H₂O(vap) and H₂O(liq) at the tabulated temperatures; (b)–(d) contactor water feeds, gas/liquid flows and compositions, and the compressor power.
Approach. The nitrogen is inert and passes through unabsorbed, so at each saturated outlet $y_{\text{H}_2\text{O}}=P^{sat}(T)/P$ fixes the water carried by the gas. An adiabatic energy balance on each contactor (with the cold liquid feed as the only free stream) sets the required water rate; the compressor duty is the enthalpy rise of the gas across it.
(a) Enthalpy table. Steam-table values converted to kJ/mol ($\times0.01802$); the vapour figures at 200–300 °C are low-pressure superheated steam:
| $\hat H$ [kJ/mol] | 300 °C | 200 °C | 40 °C | 25 °C | 20 °C |
|---|---|---|---|---|---|
| N₂ | 8.12 | 5.13 | 0.438 | 0 | −0.146 |
| H₂O (vapour) | 55.41 | 51.88 | 46.38 | 45.88 | 45.71 |
| H₂O (liquid) | — | — | 3.018 | 1.889 | 1.511 |
| Quantity | Result |
|---|---|
| (b) Liquid water to contactor 1 | 1170 mol/s (21.1 kg/s) |
| (b) Gas out / liquid out (1) | 77.9 mol/s @ $y=0.0369$ / 1192 mol/s |
| (c) Compressor power | ≈ 368 kW |
| (d) Liquid water to contactor 2 | 1357 mol/s |
| (d) Vented gas / liquid out (2) | 75.4 mol/s @ $y=0.00528$ / 1359 mol/s |
| Overall water recovery | ≈ 98.4 % |