Supported titanium dioxide‐based photocatalysts were investigated for the degradation of pharmaceuticals under irradiation with UV−A LEDs. Focus of the presented research was placed on the degradation kinetics under different matrix influences and energy flux densities of UV−A radiation. The chemical parameters, pH, orthophosphate, nitrogen concentration and background organic concentration were investigated. The results were evaluated by time‐resolved measurement of the concentrations and by calculating and plotting the first‐order degradation rate. The results showed clear differences in the rates of degradation of each compound, with diclofenac being the most easily degraded and metoprolol the most resistant. When the influence of energy flux density was examined, a linear relationship between degradation rate and the square root of energy flux density was confirmed. The organic background matrix has a strong influence on the degradation kinetics of the compounds. Nitrogen and orthophosphate slow down the degradation much less than the organic background matrix. Investigating the pH influence, it could be shown that almost no degradation is detected in the basic pH range. The results were illustrated with the help of a radar diagram, which can show all dependencies at a glance.

Hexavalent chromium (Cr(VI)) is a prevalent and highly toxic pollutant, posing a serious threat to human health and ecosystems. This study addresses this issue by exploring the photocatalytic reduction of Cr(VI) using hydrothermally synthesized nickel cobaltite (NiCo2O4) spinel–supported films. The research fills the gap for efficient visible light photocatalytic materials for Cr(VI) reduction, with the aim to synthesize, characterize, and assess NiCo2O4-supported films’ photocatalytic activity. Synthesis was achieved via a hydrothermal method on fluorine-doped tin oxide (FTO) and titanium dioxide (TiO2) over FTO substrate. The films were characterized using several techniques and their photocatalytic activity was tested under UV-A and visible light, with Cr(VI) concentration monitored periodically up to 240 min. The NiCo2O4/TiO2 film demonstrated superior photoreduction performance under both UV and visible light radiation compared to TiO2 and NiCo2O4, achieving photoreduction of Cr(VI) by 76% under UV light with a rate constant of 5.79 × 10−3 min−1 and 60% under visible light with a rate constant of 4.74 × 10−3 min−1. In conclusion, hydrothermally synthesized NiCo2O4/TiO2 film shows promising photocatalytic performance for Cr(VI) reduction, marking a significant advancement in photocatalysis and water treatment technologies. Future research will focus on stability assessment, synthesis process optimization, and real-world water treatment application.

Floating immobilized spherical titanium dioxide catalysts were used to degrade micro-pollutants by solar photocatalysis. The degradation of the micro-pollutants was performed in the secondary effluent of a wastewater treatment plant. During the experimental period, the continuous measurement of the solar ultraviolet (UV) radiation intensity was performed. The micro-pollutants were degraded to an average of 55% after 9 h of irradiation. A substance-specific degradation affinity was found, whereby degradation rates varied by a factor of up to 3.5. The substance-specific adsorption behavior was identified as a major limitation of the reaction performance. With an increasing influence of adsorption limitation, the degradation kinetics changed from the pseudo-first order to pseudo-zero order. A correlation between degradation rate and solar irradiance could only be found for substances with high degradation/adsorption affinity. For diclofenac, a 95% degradation rate could be achieved at a radiation dose of approximately 190 mWh/m². The investigated technology represents a promising possibility for a minimally invasive extension of wastewater treatment plants. Possibilities of implication were estimated and discussed within this work, whereby possibilities arise for large-scale as well as decentral treatment plants.

The effects of various additives (Y₂O₃, Ga₂O₃, and WO₃) on photocatalytic degradation efficiency under UV light-emitting diodes (LEDs) and the optical properties of TiO₂ Degussa P25 were investigated using ketoprofen and diclofenac, two non-steroidal anti-inflammatory drugs commonly detected in German rivers. Experimental results demonstrated that thin films containing these additives exhibited similar photocatalytic degradation efficiencies as pure TiO₂, achieving a 30% degradation of ketoprofen over 150 min. In contrast, the Y₂O₃/TiO₂ thin film showed significantly improved performance, achieving a 46% degradation of ketoprofen in 180 min. Notably, the Y₂O₃/TiO₂ system was three times more effective in degrading diclofenac compared to pure TiO₂. Additionally, the Y₂O₃/TiO₂ photocatalyst retained its activity over three successive cycles with only a slight decrease in efficiency. The photocatalytic degradation of both organic pollutants followed first-order kinetics with all photocatalysts. The investigation included SEM imaging to assess the surface homogeneity of the thin films and UV-vis solid-state spectroscopy to evaluate the impact of the additives on the energy band gap of TiO₂.

The photocatalytic efficiency of TiO₂ was significantly enhanced by coupling with WO₃ to form a TiO₂/WO₃ heterostructure, designed to operate effectively under UV-LED irradiation. The nanocomposites were synthesized via a hydrothermal route, and their activity was evaluated through the degradation of the pharmaceutical pollutant venlafaxine. Contaminants are rarely addressed in photocatalytic studies. Unlike a simple physical mixture of commercial TiO₂ and WO₃ powders, the hydrothermally synthesized TiO₂/WO₃ photocatalyst exhibited superior efficiency, attributable to its nanoscale dimensions achieved via the hydrothermal route, which promoted improved charge carrier separation, enhanced surface homogeneity, and the formation of an effective heterojunction interface. An optimization study varying the WO₃ content (5, 10, 20, and 30 wt.%) within the TiO₂ revealed that the 10 wt.% WO₃ composition achieved the highest performance, with ~52% venlafaxine degradation within 60 min. SEM, TEM, FTIR, Raman spectroscopy, XRD, and UV-Vis DRS revealed the successful incorporation of WO3 into the TiO₂ matrix, confirming phase purity and composition-dependent structural evolution of the nanocomposite, and evidencing extended light absorption and superior charge-transfer properties. Importantly, the optimized photocatalyst thin film retained excellent stability and reusability, maintaining high degradation efficiency over three consecutive cycles with negligible activity loss, which avoids slurry separation. These findings establish hydrothermally synthesized TiO₂/10%WO₃ thin film heterostructures as effective and sustainable photocatalytic platforms for the removal of pharmaceutical pollutants in wastewater under UV-LED irradiation.

Carrier-bound titanium dioxide catalysts were used in a photocatalytic ozonation reactor for the degradation of micro-pollutants in real wastewater. A photocatalytic immersion rotary body reactor with a 36-cm disk diameter was used, and was irradiated using UV-A light-emitting diodes. The rotating disks were covered with catalysts based on stainless steel grids coated with titanium dioxide. The dosing of ozone was carried out through the liquid phase via an external enrichment and a supply system transverse to the flow direction. The influence of irradiation power and ozone dose on the degradation rate for photocatalytic ozonation was investigated. In addition, the performance of the individual processes photocatalysis and ozonation were studied. The degradation kinetics of the parent compounds were determined using liquid chromatography tandem mass spectrometry. First-order kinetics were determined for photocatalysis and photocatalytic ozonation. A maximum reaction rate of the reactor was determined, which could be achieved by both photocatalysis and photocatalytic ozonation. At a dosage of 0.4 mg /mg DOC, the maximum reaction rate could be achieved using 75% of the irradiation power used for sole photocatalysis, allowing increases in the energetic efficiency of photocatalytic wastewater treatment processes. The process of photocatalytic ozonation is suitable to remove a wide spectrum of micro-pollutants from wastewater.