Sequential helminth egg inactivation using a solar driven advanced oxidation process (AOP) followed by chlorine was achieved. The photo-assisted Fenton process was tested alone under different H(2)O(2) and/or Fe(II) concentrations to assess its ability to inactivate Ascaris suum eggs. The effect of free chlorine alone was also tested. The lowest egg inactivation results were found using Fe(II) or H(2)O(2) separately (5 and 140 mmol L(-1), respectively) in dark conditions, which showed about 28% inactivation of helminth eggs. By combining Fe(II) and H(2)O(2) at the same concentrations described earlier, 55% of helminth egg inactivation was achieved. By increasing the reagent's concentration two-fold, 83% egg inactivation was achieved after 120 min of reaction time. Process efficiency was enhanced by solar excitation. Using solar disinfection only, the A. suum eggs inactivation reached was the lowest observed (58% egg inactivation after 120 min (120 kJ L(-1))), compared with tests using the photo-Fenton process. The use of the photo-Fenton reaction enhanced the process up to over 99% of egg inactivation after 120 kJ L(-1) when the highest Fe(II) and H(2)O(2) concentration was tested. Practically no effect on the helminth eggs was observed with free chlorine alone after 550 mg min L(-1) was used. Egg inactivation in the range of 25-30% was obtained for sequential processes (AOP then chlorine) using about 150 mg min L(-1).

In this work, the use of previously reported figures-of-merit is proposed for the comparison of solar-driven photocatalytic disinfection technologies using NF-codoped TiO2. These figures-of-merit are based on the solar collection area per order (ACO) through the understanding of the overall kinetic behavior of the disinfection process under the tested conditions: pH 7, four different catalyst concentrations (0.0, 0.10, 0.25 and 50 mgmL− 1) and two solar radiation types (UV+visible and visible radiation alone). The results provide a direct link to the accumulated energy efficiency (the lowest the value the highest the efficiency) of the inactivation process, allowing the comparison between the efficiencies of a broad range of processes evaluating different experimental conditions.

Iron-doped TiO2 nanopowders with different doping amounts have been prepared by co-precipitation method followed by heat treatment. The obtained materials were structurally, morphologically and analytically characterized by X-ray diffraction (XRD), FT-Raman spectroscopy, diffuse reflectance spectroscopy (DRS) and energy dispersive X-ray spectroscopy (EDX) coupled to scanning electron microscopy (SEM). XRD analysis revealed the major presence of the anatasa crystalline phase for iron-doped and undoped TiO2. SEM confirmed particles sizes among the nanometer scale along with XRD data. The presence of iron ions was validated by EDX-SEM. Diffuse reflectance techniques were carried out to validate the shift of the band edge absorption spectrum of doped TiO2 nanoparticles towards the visible region and to confirm the presence of iron atoms in the TiO2 crystal lattice by the resulting variation of the band gap value of the doped materials. Photocatalytic activity of the nanoparticles under UV and visible radiation was evaluated by means of hydroxyl radicals production through indirect estimation using N,N-dimethyl-p-nitrosoaniline (PNDA)photo-discoloration experiments in aqueous dispersion. Samples containing 1.2 and 5.6 weight % Fe exhibited the highest activities in this study for both conditions.