Gas–liquid
reactions (such as aqueous phase hydrogenations)
are frequently mass transport limited. Characterization of reactor
overall mass transport performance is key to the successful transfer
of reactions across scales or between plants. Despite this need, prediction
of mass-transfer performance remains elusive. In this paper, the authors
adapt the pressure step method of Teramoto et al. for use in a 1.3 m3 vessel by explicitly accounting for background pressure loss.
The method is found to produce theoretically sound results rapidly,
with measured hydrogen solubility in water agreeing well with the
literature. The measured values of the overall mass-transfer coefficient, k
L
a, are compared
to those predicted by published correlations and modeling tools, which
are found to give generally poor predictive performance.
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