Abstract

The optimal photocatalyst concentration for industrial wastewater treatment in current photoreactor designs is several hundreds of milligrams per liter. However, the elimination of emerging contaminants (ECs), which are present at extremely low concentrations in waste water treatment plants (WWTP) effluents might be accomplished at much lower catalyst (TiO2) concentrations. One of the main drawbacks of reducing catalyst loading below the optimum is the loss of useful photons which instead are transmitted through the TiO2 suspension without being absorbed by the catalyst. Accordingly, in this work, laboratory and solar pilot-scale experiments were performed with real WWTP effluents to evaluate the kinetics of photocatalytic degradation of 52 emerging contaminants under realistic (ppb) concentrations. The analysis of the samples was accomplished by solid phase extraction (SPE) followed by liquid chromatography–mass spectrometry (LC–MS). In view of the results, low concentrations of TiO2 of the order of tens of milligrams per liter were found to be insufficient for the degradation of the ECs in photoreactors with a short light-path length (29cm). However, it was established that solar reactors of diameters of several hundreds of millimetres could be used for the efficient removal of ECs from WWTP effluents. The results presented show a general methodology for selecting the most efficient reactor diameter on the basis of the desired catalyst concentration.

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