In bioreactor characterization, which standard method(s) can be used to determine the oxygen absorption (transfer) rate in a liquid culture system?

Difficulty: Easy

Correct Answer: All of these

Explanation:


Introduction / Context:
Measuring oxygen transfer is central to aerobic fermentation design and scale-up. Engineers routinely estimate volumetric mass transfer coefficients and oxygen absorption rates using chemical and biological methods. This question reviews the common laboratory/plant techniques you should recognize.


Given Data / Assumptions:

  • Well-mixed vessel; dissolved oxygen (DO) probe is available when needed.
  • Air or oxygen-enriched gas is sparged; temperature and salinity controlled.
  • Biological oxygen uptake may be present or purposely eliminated (chemical method).


Concept / Approach:
The sodium sulfite oxidation test chemically removes oxygen with a well-known stoichiometry, letting you back-calculate transfer rate. The dynamic gassing-out method strips DO to low levels and then tracks the DO rise after re-aeration to estimate kLa and absorption rate. Under steady state with known oxygen uptake rate, direct DO balance can also yield oxygen absorption/transfer rates.


Step-by-Step Solution:

Sulfite method: dose Na2SO3 plus catalyst; measure oxygen uptake; compute transfer.Dynamic gassing-out: deoxygenate, then fit DO(t) to 1 − exp(−kLa t) to obtain kLa and rate.Direct measurement: at steady state, set transfer rate = biological uptake rate by mass balance.


Verification / Alternative check:
Cross-compare estimates from chemical vs. biological methods under identical hydrodynamics; values should agree within experimental error if probe response is accounted for.


Why Other Options Are Wrong:

  • Saying only one method works ignores standard practice.
  • “None”: contradicts decades of reactor testing methodology.


Common Pitfalls:
Neglecting probe lag, temperature correction, or catalyst presence in sulfite tests; misfitting DO transients.


Final Answer:
All of these.

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