23-Chem-B4 Biochemical Engineering · Undated paper
Question 1 of 5: Maximum Oxygen-Transfer Flux in a Stirred-Tank Bioreactor
Nivaar worked solution (AI-drafted; not reviewed by a licensed engineer)
Notes on this paper
National Exam 16-Chem-B4, Biochemical Engineering — May 2019 (the header on page 1 reads "16-Chem-B4/May 2019"). 3 hours, Closed-Book Exam (approved Casio or Sharp calculator
permitted). Per the exam notes, FIVE (5) questions constitute a complete paper and all five must be answered;
each question is of equal value (20 marks) and short-essay-format answers are marked for clarity and
organization.
Interpretation notes: Two points where the printed question itself needs an interpretation are flagged where they are used: the meaning of p in the Question 1 solubility equation, and the definition of the observable Thiele modulus in Question 3.
Question 1: Maximum Oxygen-Transfer Flux in a Stirred-Tank Bioreactor (20 marks)
Find. The maximum volumetric oxygen-transfer rate OTRmax (g O₂ per m³
per h) the impeller/sparger system can supply to the broth.
Fig. 1 — single Rushton-turbine stirred tank with sparged air; OTRmax is set
by the achievable kLa at this power input and the saturation driving force from the sparged air.
Approach. Compute the impeller power draw from the given power number, apply the
gassed/ungassed ratio to get Pg, use the given empirical correlation to convert volumetric power input
into kLa, and combine with the maximum achievable driving force (saturation dissolved oxygen, taking
the bulk liquid as oxygen-free) to get the maximum transfer flux.
Impeller (ungassed) power draw. Rearranging the given power-number definition,
$$P=N_p\,\rho\,N^3D^5=6\times1000\times(1)^3\times(0.936)^5$$
$$P=6000\times0.71840\ \text{W}=\boxed{4310.5\ \text{W}}$$
(Reynolds number $N_{Re}=\rho N D^2/\mu=1000\times1\times0.936^2/10^{-3}=8.76\times10^5$, fully turbulent —
consistent with using a constant power number.)
Gassed power and volumetric power input. With Pg/P = 0.6,
$$P_g=0.6\times4310.5=2586.3\ \text{W}=2.5863\ \text{kW}$$
$$\frac{P_g}{V_L}=\frac{2.5863\ \text{kW}}{10\ \text{m}^3}=0.25863\ \text{kW/m}^3$$
Volumetric mass-transfer coefficient. Substituting into the given correlation
(Pg/VL in kW/m³, kLa in s−1),
$$k_La=9.09\times10^{-4}\left(\frac{P_g}{V_L}\right)^{0.7}=9.09\times10^{-4}\times(0.25863)^{0.7}$$
$$k_La=9.09\times10^{-4}\times0.3881=\boxed{3.528\times10^{-4}\ \text{s}^{-1}}\ (=1.270\ \text{h}^{-1})$$
Saturation dissolved-oxygen concentration. The question labels P and p as the total and the
(oxygen) partial pressure, so for air at 1 atm $P=760$ Torr and $p=y_{O2}P=0.21\times760=159.6$ Torr. At
$t=20^\circ$C, which is inside the stated 0–30 °C range,
$$DO^*=\frac{(P-p)\times0.678}{35+t}=\frac{(760-159.6)\times0.678}{35+20}=\frac{600.4\times0.678}{55}$$
$$\boxed{DO^*=7.401\ \text{ppm}=7.401\ \text{g/m}^3}$$
(1 ppm ≈ 1 mg/L = 1 g/m³ in dilute aqueous solution.)
Assumption (exam Note 1): p is used exactly as the question labels it, the
oxygen partial pressure. The equation is the classical formula for air-saturated water, in which p is normally the saturated
water-vapour pressure at t. On that reading p = 17.54 Torr at 20 °C, giving DO* = 9.15 ppm (close to the
tabulated 9.1 mg/L) and OTRmax = 11.6 g O₂/(m³·h). The method is identical; only the
driving force changes.
Maximum volumetric oxygen flux. The flux is largest when the bulk liquid holds no dissolved
oxygen ($C_L=0$), so the full saturation value is the driving force. Converting kLa to per hour for
the requested units,
$$OTR_{max}=k_La\,(DO^*-0)=3.528\times10^{-4}\ \text{s}^{-1}\times3600\ \text{s/h}\times7.401\ \text{g/m}^3$$
$$\boxed{OTR_{max}=9.40\ \text{g O}_2/(\text{m}^3\cdot\text{h})}$$