Persistent and mobile (PM) substances are being recognized as serious threats to water resources and drinking water suppliers have to use advanced treatment if raw waters are contaminated with such compounds. In this study, analytical methods for 25 micropollutants for which insufficient or no data on their occurrence in surface waters and on their behavior during drinking water treatment were available, were developed. More than 120 surface water samples were analyzed and laboratory tests were performed to evaluate the compounds' behavior during aerobic bank filtration (BF), activated carbon treatment, and ozonation. Ensulizole, 1,3-diphenylguanidine and 2-acrylamido-2-methylpropane sulfonic acid revealed the highest detection frequencies in the Rhine river. Concentration level and detection frequency correlated positively with the wastewater fraction. However, street run-off is likely an additional discharge pathway for 1,3-diphenylguanidine. In simulated BF, seven (six) substances could be classified as persistent (very persistent). By applying powdered activated carbon, 42% of the substances were well removed as was the case for 50% of the compounds when applying 0.2 mg/L O3. In total, eight of the substances detected in surface waters were weakly removed by at least one of the investigated removal processes and may cause problems for drinking water suppliers.

In the present work, a suitable experimental setup was developed to successfully apply advanced oxidation processes (AOP) to real groundwater matrices. This setup combines an O₃-bubble column reactor with a carrier-bound TiO₂/UV-system. The degradation of various chlorinated ethene and methane derivatives commonly found of chlorinated volatile organic compound polluted regional groundwater samples was investigated. Because of known issues within water remediation using AOP such as toxification by transformation products, this study aimed at complete mineralization of the contained organic micropollutants. Moreover, the influences of variable process parameters such as flow rate, ozone concentration, and radiation dose on process performance were statistically evaluated and discussed. Parameter optimization using a Box-Behnken experimental design resulted in very promising degradation rates. It was thus possible to achieve a degradation rate of at least 98% for cis-dichloroethene, trichloroethene and tetrachloroethene and 85% for trichloromethane without formation of transformation products. The results of this work open up the possibility of developing innovative technologies based on AOP, which can be universally applied even to challenging matrices such as groundwater.

Photocatalytic disintegration is a novel approach to eliminate pollution. The method utilizes the semiconductor titanium dioxide to degrade organic molecules in the presence of ultraviolet (UV) light. In this study, it is shown how the capabilities of several types of catalyst designs degrade the non-polar substance diesel fuel and the polar substance methylene blue. The floating design of foam glass coated with titanium dioxide could reduce the concentration of diesel fuel by 329 mg/L in 16 h; the submerged designs for coated glass fiber and coated steel grit could reduce methylene blue concentration by 96.6% after 4 h and 99.1% after 6 h, respectively. It could be shown that photocatalysis is a promising cost- and energy-efficient method for managing air and water pollution. It can be established as a low-technology method without requiring the use of a conventional source of energy, given an adequate amount of sun hours, or as an additional cleaning stage in water treatment plants using UV-LEDs.

Supported titanium dioxide catalysts were used in a photocatalytic flat cell reactor to remove organic micropollutants from real wastewater. Catalysts based on stainless steel mesh with a porous coating made of titanium dioxide nanoparticles with predominantly anatase modification were used. The influence of the retention time, and light output, and the effect of hydrogen peroxide on the degradation were examined. The kinetics of the degradation of the parent substances was determined by liquid chromatography-tandem mass spectrometry. As a result, first-order degradation kinetics could be confirmed for all substances. The irradiance had no linear influence on the degradation of the compounds. Hydrogen peroxides were added to the wastewater to be treated, as electron acceptors and boosters, and alone had no great oxidative effect on the parent substances. The combination of photocatalysis with the addition of hydrogen peroxide as an electron acceptor had great synergetic effects which can reduce the required energy of the process through a short retention time. The process is suitable for the removal of micropollutants from wastewater.

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.