Instrumented 3.0 L Glass Stirred-Tank Bioreactor
2.0 L working volume vessel with 4 vertical baffles, ring sparger, and Rushton turbine.
Determine the volumetric gas–liquid oxygen mass transfer coefficient k_L a in an aerated, agitated stirred-tank fermenter using the dynamic gassing-out method with a fast-response dissolved oxygen probe as a function of impeller agitation speed N. Explore interactive transport phenomena, unit operations simulation, and chemical engineering telemetry.
Ready to sample with Agitation N = 300.0 RPM.
Adjust Agitation N, then execute chemical process trial.
Chemical and process engineering telemetry is evaluated rigorously using 64-bit IEEE 754 precision. Residuals reflect ordinary least-squares regression across successive observations. Continuous data structures support high-fidelity transport phenomena and unit operations modeling.
The transport and thermodynamic models apply within the specified calibrated operating window (100.0 to 600.0 RPM). Evaluated using a 3.0 L glass fermenter (liquid volume V_L = 2.0 L, Rushton turbine D_i = 45 mm, ring sparger) sparged with air at 1.0 vvm (2.0 L/min) and 25.0 °C. Linear regression models k_L a versus N^1.2 to extract slope S = 0.0240 h^-1/RPM^1.2.
2.0 L working volume vessel with 4 vertical baffles, ring sparger, and Rushton turbine.
Measures dissolved oxygen percentage from 0 to 100% saturation with 0.1% accuracy and t_90 < 2 s.
Switches instantaneously between nitrogen gas (deoxygenation) and clean compressed air (reoxygenation).
Maintains precise agitation speeds from 100 to 600 RPM with ±1 RPM accuracy.
Maintains aqueous broth at constant temperature 25.00 ± 0.05 °C.
Logs DO reoxygenation curves at 5 Hz and computes k_L a via real-time linear regression.
Determine the volumetric gas–liquid oxygen mass transfer coefficient k_L a in an aerated, agitated stirred-tank fermenter using the dynamic gassing-out method with a fast-response dissolved oxygen probe as a function of impeller agitation speed N. Standardized parameter settings: 100.0, 200.0, 300.0, 400.0, 500.0, 600.0 RPM.
Calibrate the DO probe at 0% saturation using zero-oxygen sodium sulfite solution (0.1 M Na2SO3 with CoCl2 catalyst) and 100% saturation in air-saturated water at 25.0 °C.
Fill reactor with 2.0 L of deionized water; set water jacket to 25.0 °C and turn on Rushton impeller at target test speed.
Sparge nitrogen gas at 2.0 L/min through the ring sparger until dissolved oxygen C_L drops below 1.0% saturation.
Instantly switch gas supply from nitrogen to compressed air at 2.0 L/min (1.0 vvm, t = 0); log transient DO percentage C_L(t) at 5 Hz.
Plot ln[(C* - C_L) / C*] versus time t over the 20% to 80% DO window to extract volumetric mass transfer coefficient k_L a.
Repeat dynamic reoxygenation procedure at impeller speeds N = 100, 200, 300, 400, 500, and 600 RPM; plot k_L a versus N^1.2 to determine slope S.
Points are your recorded observations. The solid regression line validates Bioreactor Oxygen Transfer k_L a mathematical scaling.
| # | Impeller Agitation Speed N (RPM) | Mass Transfer Factor (k_L a) (h^-1) | Agitation speed factor N^1.2 (RPM^1.2) | Volumetric oxygen mass transfer coefficient k_L a (h^-1) | Remove |
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In industrial bioprocess engineering, aerobic fermentation (e.g., antibiotic synthesis, monoclonal antibody production, yeast cultivation, and wastewater bio-oxidation) requires continuous delivery of dissolved oxygen to metabolizing microbial cells. Because oxygen is sparingly soluble in aqueous nutrient broths (saturation concentration C* is only ~8.0 mg/L at 25 °C), the rate of biological oxygen consumption by dense cultures can deplete dissolved oxygen in seconds unless oxygen is continuously transferred across the gas-liquid interface. The volumetric rate of oxygen transfer (OTR) is governed by two-film mass transfer theory: OTR = k_L a · (C* - C_L), where k_L is the liquid-side film mass transfer coefficient, 'a' is the specific gas-liquid interfacial area per unit liquid volume, C* is saturation dissolved oxygen concentration, and C_L is bulk dissolved oxygen concentration. The lumped parameter k_L a (units h^-1) represents the aeration capacity of the bioreactor. In the dynamic gassing-out method, liquid is first deoxygenated by sparging nitrogen gas until C_L = 0; nitrogen is then shut off, air sparging is initiated, and the transient reoxygenation curve C_L(t) is recorded using a fast-response polarographic dissolved oxygen (DO) probe: dC_L / dt = k_L a · (C* - C_L) -> ln[(C* - C_L(t)) / C*] = -k_L a · t. According to van't Riet's classical correlations for aerated stirred tanks, volumetric mass transfer coefficient k_L a scales with mechanical agitation speed as N^1.2 and superficial gas velocity as v_s^0.5: k_L a ∝ (P_g / V)^0.4 · v_s^0.5 ∝ N^1.2. In this laboratory investigation, an instrumented 3.0-liter glass stirred-tank bioreactor is operated across impeller speeds from 100 to 600 RPM at constant air sparging rate to measure reoxygenation curves, verify N^1.2 scaling, and determine the aeration scaling slope S = 0.0240 h^-1/RPM^1.2.
Evaluated using a 3.0 L glass fermenter (liquid volume V_L = 2.0 L, Rushton turbine D_i = 45 mm, ring sparger) sparged with air at 1.0 vvm (2.0 L/min) and 25.0 °C. Linear regression models k_L a versus N^1.2 to extract slope S = 0.0240 h^-1/RPM^1.2.