The concept of coabsorption of NO2 and SO2 from flue gases, in combination with the
enhanced oxidation of NO
by ClO2(g), is studied on three scales, 0.2, 100, and 400
N m3/h, all with flue gases of different origins. The results
obtained from each setup are presented, together with modeling that
was applied to assess the scale-up of the concept and to validate
the model. The measurements confirm that ClO2 is highly
selective toward NO oxidation for temperatures in the range of 70–155
°C. A comparison of the results obtained for each scale reveals
that the 0.2 N m3/h setup confers a higher level of NO
x
absorption than the other setups, although
the trends remain similar. Simulations of the results underpredict
the level of NO2 absorption in the 0.2 N m3/h
setup while capturing the levels of absorption in the 100 N m3/h setup. An important finding is the rapid and complete oxidation
of S(IV) in the presence of NO2, which is not represented
in the reaction kinetics.