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23-Chem-A1 Process Balances and Chemical Thermodynamics · May 2015

Question 3 of 7: Two-Stage Water Recovery with Interstage Compression

Nivaar worked solution (AI-drafted; not reviewed by a licensed engineer)

Notes on this paper

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 3: Two-Stage Water Recovery with Interstage Compression (Part B — 25 marks)

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.

Contactor 12 barCompressorContactor 26 barFeed 100 mol/s0.75 N2/0.25 H2O300 C, 2 barLiquid H2O 20 Cgas 40 C, 2 barliquid out 40 C200 C, 6 barLiquid H2O 20 Cgas out 25 C6 bar (dry)liquid out 25 C
Figure 3 — Two-stage water recovery: first contactor (2 bar, gas out 40 C), interstage compression to 6 bar/200 C, second contactor (6 bar, gas out 25 C).

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 °C200 °C40 °C25 °C20 °C
N₂8.125.130.4380−0.146
H₂O (vapour)55.4151.8846.3845.8845.71
H₂O (liquid)——3.0181.8891.511
  1. (b) Water carried out of contactor 1. Saturation at 40 °C, 2 bar gives $y_1=P^{sat}(40)/P=0.0738/2=0.0369$. With 75 mol/s N₂ inert, $$\dot n_{G,1}=\frac{75}{1-y_1}=77.9\ \text{mol/s},\qquad \dot n_{w,\text{gas}}=77.9(0.0369)=2.87\ \text{mol/s}.$$
  2. Energy balance on contactor 1 (adiabatic ⇒ $\dot H_{in}=\dot H_{out}$). The only unknown is the liquid feed $\dot n_{\text{H}_2\text{O},1}$ (20 °C in, 40 °C out): $$75(8.12)+25(55.41)+\dot n_1(1.511)=75(0.438)+2.87(46.38)+\dot n_2(3.018),$$ with water balance $\dot n_2=25+\dot n_1-2.87$. Solving, $$\dot n_{\text{H}_2\text{O},1}=\boxed{1170\ \text{mol/s}\;(=21.1\ \text{kg/s})},\qquad \dot n_2=1192\ \text{mol/s liquid out}.$$ Leaving gas: 77.9 mol/s at $y_{\text{H}_2\text{O}}=0.0369$ (75 N₂ + 2.87 H₂O).
  3. (c) Compressor power. The compressor raises the 40 °C gas to 200 °C; adiabatic shaft work equals the enthalpy rise (N₂ + its 2.87 mol/s water): $$\dot W=75(5.13-0.438)+2.87(51.88-46.38)=351.9+15.8=\boxed{368\ \text{kW}}.$$
  4. (d) Second contactor. Saturation at 25 °C, 6 bar gives $y_2=P^{sat}(25)/6=0.03169/6=0.00528$, so $$\dot n_{G,2}=\frac{75}{1-y_2}=75.4\ \text{mol/s},\qquad \dot n_{w,\text{gas,2}}=0.398\ \text{mol/s}.$$ Energy balance (gas in 200 °C, out 25 °C; liquid in 20 °C, out 25 °C) with $\dot n_4=2.87+\dot n_3-0.398$: $$75(5.13)+2.87(51.88)+\dot n_3(1.511)=75(0)+0.398(45.88)+\dot n_4(1.889)\;\Rightarrow\;\dot n_{\text{H}_2\text{O},3}=\boxed{1357\ \text{mol/s}},\ \dot n_4=1359\ \text{mol/s}.$$ The vented gas carries only 0.398 mol/s water — 98.4 % of the original 25 mol/s has been recovered.
QuantityResult
(b) Liquid water to contactor 11170 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 21357 mol/s
(d) Vented gas / liquid out (2)75.4 mol/s @ $y=0.00528$ / 1359 mol/s
Overall water recovery≈ 98.4 %