ABSTRACT
Hydrochlorothiazide (HCT) is a pharmaceutical micropollutant highly toxic to the environment, being absolutely necessary to oxidize it completely to CO2. Here, the variables stoichiometric H2O2 excess for (a) degradation and (b) mineralization are defined and used as metric to quantify the dosimetry of the H2O2. So that, dose of H2O2 qualifies being under- and over-dose respectively for values below and above such standards. In this work, these concepts have been elucidated across AOPs regarding the H2O2 degradation excess, whereas only UVC-Fenton was used regarding the H2O2 mineralization excess. At a H2O2 mineralization excess of 0.68 (equivalent to degradation excess of 36.74), oxidation via UVC-H2O2 enables absolute (100%) HCT degradation within 60 min; however, the mineralization of HCT demonstrated limited optimization for all AOPs employed in the beaker-like reactor of this work, being the underlying reasons investigated hereby. At best, 26.70% HCT mineralization was observed within 60 min of UVC photo-Fenton using an initial 2.00 H2O2 mineralization excess. Such mineralization of 26.7% is unexpectedly low considering that, in addition, the residual H2O2 concentration almost fully depletes within 30 min of UVC-Fenton oxidation. Taken all that together, the loss of H2O2 due its decomposition induced by the risen temperature from 28 to 70ºC very likely were the underlying reason preventing better mineralization performance. We successfully demonstrated 18% of mean efficiency of radical â¢OH consumption signals that the overheating is indeed a designer problem with the photo-reactor since a well-refrigerated photo-reactor shows a mean efficiency of 38% for the same H2O2 excess.
