Ibuprofen (IBP) is an anti-inflammatory drug whose residues can be found worldwide in natural water bodies resulting in harmful effects to aquatic species even at low concentrations. This paper deals with the degradation of IBP in water by hydrodynamic cavitation in a convergent-divergent nozzle. Over 60% of ibuprofen was degraded in 60 min with an electrical energy per order (EEO) of 10.77 kWh m(-3) at an initial concentration of 200 μg L(-1) and a relative inlet pressure pin=0.35 MPa. Five intermediates generated from different hydroxylation reactions were identified; the potential mechanisms of degradation were sketched and discussed. The reaction pathways recognized are in line with the relevant literature, both experimental and theoretical. By varying the pressure upstream the constriction, different degradation rates were observed. This effect was discussed according to a numerical simulation of the hydroxyl radical production identifying a clear correspondence between the maximum kinetic constant kOH and the maximum calculated OH production. Furthermore, in the investigated experimental conditions, the pH parameter was found not to affect the extent of degradation; this peculiar feature agrees with a recently published kinetic insight and has been explained in the light of the intermediates of the different reaction pathways.
Numerical simulation of sorption dynamics showed that the use of data recorded at (or very close to) equilibrium in the search for the kinetic equation that best describes the process frequently leads to incorrect conclusions. Notably, it has been demonstrated that the fit of the adsorption data at equilibrium (t/q t versus t) is a straight line irrespective of the sorption kinetics. In order to distinguish pseudo-first-order from pseudo-second-order sorption kinetics, the data near the equilibrium should be omitted from the least-squares fit and the result confirmed by a different method. A straightforward method based on ∆(q t /q e )/∆t versus 1 -q t /q e and versus (1 -q t /q e ) 2 plots is suggested. Some recent papers reporting incorrect sorption kinetic analyses are discussed.
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