PFAS substances, which have been under investigation in recent years, are certainly some of the most critical emerging contaminants. Their presence in drinking water, correlated with diseases, is consistently being confirmed by scientific studies in the academic and health sectors. With the aim of developing new technologies to mitigate the water contamination problem, research activity based on advanced oxidation processes for PFAS dealkylation and subsequent mineralization is active. While UV radiation could be directly employed for decontamination, there are nevertheless considerable problems regarding its use, even from a large-scale perspective. In contrast, the use of cheap, robust, and green photocatalytic materials active under near UV-visible radiation shows interesting prospects. In this paper we take stock of the health problems related to PFAS, and then provide an update on strategies based on the use of photocatalysts and the latest findings regarding reaction mechanisms. Finally, we detail some brief considerations in relation to the economic aspects of possible solutions.

As the effectiveness of conventional wastewater treatment processes is increasingly challenged by the growth of industrial activities, a demand for low-cost and low-impact treatments is emerging. A possible solution is represented by systems coupling solar concentration technology with advanced oxidation processes (AOP). In this paper, a review of solar concentration technologies for wastewater remediation is presented, with a focus on photocatalyst materials used in this specific research context. Recent results, though mostly on model systems, open promising perspectives for the use of concentrated sunlight as the energy source powering AOPs. We identify (i) the development of photocatalyst materials capable of efficiently working with sunlight, and (ii) the transition to real wastewater investigation as the most critical issues to be addressed by research in the field.

In this study, a sustainable method employing concentrated sunlight to achieve environmental remediation of wastewater, contaminated by Ciprofloxacin antibiotic (CIP), is thoroughly investigated. A green ZnO/g-C₃N₄ nanocomposite (NC) is used as a photocatalyst coating on glass to investigate the inactivation of CIP in water, in a flow-reactor configuration at small-prototype scale (10 liters/h, catalyst area 187.5 cm²). ZnO/g-C₃N₄ NC coatings were obtained by an in-situ thermal condensation process coupled with a green synthesis protocol and deposited on glass, via a simple drop casting method. Morphological and structural analyses of synthesized composites were performed with Fourier-Transform Infrared (FTIR) Spectroscopy, Scanning Electron Microscopy (SEM), Energy-Dispersive X-ray (EDX) and X-ray diffraction (XRD) techniques, while optical properties were studied with Diffuse Reflectance Spectroscopy (DRS). The degradation of CIP was first tested at a lab scale under simulated sunlight and then studied under sunlight in a parabolic trough concentrator (PTC). Suitable degradation of CIP (100%) was observed at 210 min via High-Performance Liquid Chromatography (HPLC) and the by-products were determined by Liquid Chromatography-Mass Spectroscopy (LC-MS). Microbiological tests revealed the absence of antibacterial activity in CIP water treated with ZnO/g-C₃N₄ NC photocatalyst against Staphylococcus aureus, Pseudomonas aeruginosa, and Priestia megaterium. Our results directly demonstrate the effective inactivation of CIP with a process designed for sustainability both in terms of energy input (solar) and scalability of materials. Also, the small-prototype scale of this investigation provides insights into the challenges arising from the perspective scale-up to an industrial application, aimed at antibiotics inactivation in wastewater and thus helping to prevent the spread of antimicrobial resistance (AMR).