The basic principles of a steady-state mass transfer
model and
the resistance-in-series film model are assessed with the aid of a
series of experiments in a gas–liquid contact membrane mini-module
(3 M Liqui-Cel MM-1.7 × 5.5) using an aqueous solution of diethanolamine
(DEA) of 0.25 M (mol/L) for biogas upgrading. Experimental data show
that CO2 removal may exceed 67% and reach 100% in combination
with the highest possible recovery of CH4 when employing
biogas flow rates in the range of 2.8 × 10–5 – 3.6 × 10–5 m3/s and solvent
flow rates within 0.47 × 10–5 – 0.58
× 10–5 m3/s. For the experimental
data set, a correlation has been developed, effectively interpolating
CO2 removal with the gas and liquid flow rates. The wetting
values calculated are concentrated close to each other for the same
liquid flow rate without considerably depending on the gas flow rate,
especially when applying the Hikita–Yun (reaction rate–shell-side
correlation) compared with the Hikita–Costello pair. Furthermore,
the calculated wetting diminishes with increasing liquid flow rate,
a result that is consistent with previous modeling attempts and relevant
literature indications. The assumption of enhanced mass transfer in
the liquid-filled part of the membrane pores due to the reaction is
scrutinized, leading to objectionable computational wetting values.
It is shown that for a concentration of DEA equal to 0.25 M the Hatta
numbers and the enhancement factors are not equal in the whole reaction
path; thus, the choice of the shell-side correlation has an appreciable
impact on the overall analysis, especially for the determination of
the wetting values.