The creation of free radicals by ultrasonic cavitation is the main mechanism that leads to chemical degradation of target pollutants and the process is considered an alternative advanced oxidation technology. The goal of this study was to compare the effects of batch and continuous flow ultrasonic systems on the formation of hydroxyl radicals. Ultrasonic batch experiments were conducted in two reactors (small and large) using a standard 20kHz catenoidal titanium horn at varying amplitudes and sonication times. The effect of saturating gas was also investigated by introducing helium and air at 1Lmin(-1) into the larger 100mL reactor. In the continuous flow system, the experiments were conducted with a 20kHz, 3.3kW ultrasonic systems using a titanium "donut" horn at varying volumetric flow rates and amplitudes. Formation of hydroxyl radicals was determined using terephthalic acid dosimetry measurements. At the same energy densities, higher hydroxyl radical concentrations were formed in the batch system than in the continuous flow system. Sonication time appeared to be the main factor that influenced the results in batch and continuous flow systems. The two gases (helium and air) did not increase the hydroxyl radical formation at any amplitude or sonication time tested.

The kinetic investigation of photodegradation of the natural organic matter (NOM) in natural lake water was conducted using two low‐pressure mercury lamps of the same nominal power: a) with suprasil quartz envelope emitting at both wavelengths −254 nm and 185 nm (hereafter VUV); b) with standard quartz envelope emitting only at 254 nm (hereafter UV). In comparison to the UV process, the addition of 185 nm irradiation (VUV process) increased the degradation rate ten‐fold overall at lower and seventeen‐fold at higher Reynolds numbers, respectively. The hydrodynamic characteristics of the photoreactor are of crucial importance for total energy efficiency for VUV processes.

Pharmaceuticals are characterized by a wide range of physical, chemical, and biological properties and functionalities that contribute to their inherent complexity as compounds. Unfortunately, human carelessness during the production, use, and disposal of these compounds results in their presence in the environment. This study utilized a nanostructured TiO₂ film on a glass ring at the bottom of a reactor and simulated a solar radiation lamp as the radiation source for both photocatalytic and photolytic experiments, with the aim of unraveling the mechanism behind the degradation of trimethoprim (TMP), a pharmaceutical compound. This approach provides a novel perspective on the role of TiO₂ in the degradation of pharmaceuticals and could pave the way for more efficient and sustainable wastewater treatment methods. Scavenger studies were carried out using isopropanol, ammonium oxalate, and triethanolamine to examine the photocatalytic mechanism. Isopropanol and triethanolamine were found to impede the photocatalytic degradation of TMP, highlighting the significance of hydroxyl radicals and positive holes in the degradation process, while no inhibition was observed in the presence of ammonium oxalate. The complete degradation of TMP through photocatalysis under simulated solar radiation was observed in ultra-pure water in fewer than 3 h, as indicated by the results. Our findings suggest that utilizing natural solar radiation as a source of UV-A radiation in reactor configurations based on this approach holds promise for cost-effective pharmaceutical degradation treatment in wastewater treatment plants. The practical potential of this approach is supported by the results obtained under simulated solar radiation with an irradiation intensity in the UV-A region of 33 ± 2 W/m².