Polluting the natural water resources is a serious global issue, which is confirmed by the fact that today at least 2 billion people consume water from contaminated sources. The conventional wastewater treatment methods cannot effectively remove the persistent pollutants (e.g., drugs, organic dyes, pesticides) from the aqueous environment. Heterogeneous photocatalysis is a promising and sustainable alternative for water remediation. It is based on the interaction between light irradiation and the semiconductors (e.g., TiO₂, ZnO) as photocatalysts, but these compounds, unfortunately, have some disadvantages. Hence, great attention has been paid to the nanotechnology as a possible way of improvement. Nanomaterials have extraordinary properties; however, their conventional synthesis is often difficult and requires a significant amount of dangerous chemicals. This concise topical review gives recent updates and trends in development of sustainable and green pathways in the synthesis of nanomaterials, as well as in their application for water remediation. In our review we put emphasis on the eco-friendly, mostly plant extract-based materials. The importance of this topic, including this study as well, is proved by the growing number of publications since 2018. Due to the current serious environmental issues (e.g., global warming, shortage of pure and quality water), it is necessary for the traditional TiO₂ and ZnO semiconductors to be replaced with the harmless, non-toxic, and more powerful nanocomposites as photocatalysts. Not only because of their higher efficiency as compared to the bulk semiconductors, but also because of the presence of biomolecules that can add up to the pollutant removal efficiency, which has been already confirmed in many researches. However, despite the fact that the application of heterogeneous photocatalysis together with green nanotechnology is absolutely the future in water purification, there are some challenges which have to be overcome. The exact effects of the biomolecules obtained from plants in the synthesis of nanoparticles, as well as in the photocatalytic processes, are not exactly known and require further investigation. Furthermore, heterogeneous photocatalysis is a well-known and commonly examined process; however, its practical use outside the laboratory is expensive and difficult. Thus, it has to be simplified and improved in order to be available for everyone. The aim of our review is to suggest and prove that using these bio-inspired compounds it is possible to reduce human footprint in the nature.

The increasing presence of various organics poses significant threats to aquatic ecosystems and living organisms. Conventional water treatment methods are often insufficient, necessitating the development of powerful and sustainable alternatives. This study addresses this challenge by exploring the synthesis of ZnO nanoparticles using green tea leaves extract—an eco-friendly approach—for the sunlight-activated removal of organics in agri-food wastewater. The research examined different conditions for the removal of clomazone (CLO), tembotrione (TEM), ciprofloxacin (CIP), and zearalenone (ZEA). Nitrate-derived ZnO synthesized in a water medium (N-gZnO_w) exhibited the highest photocatalytic activity, removing 98.2, 95.8, 96.2, and 96.6% of CLO, TEM, CIP, and ZEA. Characterization techniques (XRD, Raman spectroscopy, SEM, zeta potential measurements, UV–visible spectroscopy) confirmed the synthesis of N-gZnO_w, with an average particle size of 14.9 nm, an isoelectric point of 9.9, and a band gap energy of 2.92 eV. Photocatalytic experiments identified 0.5 mg/cm³ as an optimal catalyst loading, while a higher initial pollutant concentration reduced degradation efficiency. LC-ESI-MS/MS measurements confirmed the efficient pollutant degradation and the formation of degradation intermediates. Hence, this study demonstrates that green tea extract-synthesized ZnO nanoparticles offer a promising, sustainable solution for removing herbicides, pharmaceuticals, and mycotoxins from wastewater, paving the way for eco-friendly water purification technologies.

Clear and sanitarily adequate water scarcity is one of the greatest problems of modern society. Continuous population growth, rising organics concentrations, and common non-efficient wastewater treatment technologies add to the seriousness of this issue. The employment of various advanced oxidation processes (AOPs) in water treatment is becoming more widespread. In this review, the state-of-the-art application of three AOPs is discussed in detail: photocatalysis, sonophotolysis, and sonophotocatalysis. Photocatalysis utilizes semiconductor photocatalysts to degrade organic pollutants under light irradiation. Sonophotolysis combines ultrasound and photolysis to generate reactive radicals, enhancing the degradation of organic pollutants. Sonophotocatalysis synergistically combines ultrasound with photocatalysis, resulting in improved degradation efficiency compared to individual processes. By studying this paper, readers will get an insight into the latest published data regarding the above-mentioned processes from the last 10 years. Different factors are compared and discussed, such as degradation efficiency, reaction kinetics, catalyst type, ultrasound frequency, or water matrix effects on process performance. In addition, the economic aspects of sonophotolysis, photocatalysis, and sonophotocatalysis will be also analyzed and compared to other processes. Also, the future research directions and potential applications of these AOPs in wastewater treatment will be highlighted. This review offers invaluable insights into the selection and optimization of AOPs.

Pure water scarcity is an emerging, all-around problem that globally affects both the life quality and the world’s economy. Heterogeneous photocatalysis under solar irradiation is a promising technique for the organic pollutants (e.g., pesticides, drugs) removal from an aqueous environment. Furthermore, the drawbacks of commercially available photocatalysts can be successfully overcome by using innovative nanoparticles, such as ZrO₂/Fe₃O₄. Four ZrO₂/Fe₃O₄ nanopowders with a different mass ratio of ZrO₂ and Fe₃O₄ were synthesized using the chemical co-precipitation method. XRD analysis showed the presence of magnetite and hematite Fe-oxide phases in all samples. The content of the magnetite phase increased with the addition of 19% ZrO₂. The efficiency of the newly synthesized ZrO₂/Fe₃O₄ nanoparticles was investigated in the rapid removal of selected pollutants under various experimental conditions. Nevertheless, the influence of the water matrix on photocatalytic degradation was also examined. The obtained data showed that using ZrO₂/Fe₃O₄ nanosystems, an appropriate removal rate of the selected pesticides and pharmaceuticals can be reached after 120 min of solar irradiation. Further, the total organic carbon measurements proved the mineralization of the target emerging pollutants. ZrO₂/Fe₃O₄ nanoparticles are economically feasible, as their removal from the suspension can be easily achieved using affordable, environmentally-friendly magnetic separation.

A new titanium/molybdenum/mixed-oxides (TMO) contact-type heterojunction photocatalyst was prepared by a simple, low-cost, and environmentally-friendly mixing-calcination solid-state method. A microstructural investigation by scanning electron microscopy (SEM) showsirregularly shaped agglomerated morphology of TMO that consists of firmly connected globular TiO₂ and rod-like MoO₃ particles. The detailed structure and optical bandgap investigation by X-ray diffraction, Raman, and UV-Vis spectroscopy revealed the TMO’s composition of ~37 wt.% rutile TiO₂, ~25 wt.% of anatase TiO₂, and ~38 wt.% of molybdite MoO₃ phase and an absorption threshold of around 380 nm, which implies more probability of desirable higher visible light absorption. The removal efficiency of pesticides quinmerac (QUI) and tembotrione (TEM), and pharmaceuticals metoprolol (MET), amitriptyline (AMI), ciprofloxacin (CIP),and ceftriaxone (CEF) from water in the presence of starting pure TiO₂, MoO₃, and prepared TMO were investigated under different pH values and UV irradiation/simulated sunlight (SS). Each starting metal-oxide precursors and prepared TMO showed a different affinity for adsorption of tested pesticides and pharmaceuticals, and, in general, better photocatalytic degradation efficiency under UV irradiation than under simulated sunlight. The highest photocatalytic degradation efficiency under UV irradiation was 81.6% for TEM using TMO; using TiO₂ was 65.0% for AMI, and using MoO₃ was 79.3% for CEF after 135 min. However, TMO showed a very high synergic adsorption/photocatalytic under-SS efficiency in the removal of CIP of almost 80% and under UV irradiation of 90% CIP removal after 75 min. The toxicity of catalysts, starting compounds, and their intermediates formed during the removal process was assessed using a rat hepatoma cell line (H-4-II-E). The highest hepatotoxic effects were obtained by using UV irradiated QUI and MET suspension with TMO for up to 60 min.

In recent years, much attention has been paid to pharmaceuticals as potential toxic bioactive substances in the worldwide environment. These compounds are continuously introduced into the surroundings in small concentrations, which certainly affects the quality of water, ecosystem, and the general health of living organisms. Photocatalysis is a promising technique for treating pharmaceutically active compounds as organic pollutants over traditional technologies. This study proposes the application of photocatalysts composed of zinc oxide (ZnO) and tin oxide (SnO₂), synthesized using a solid-state method, for the photocatalytic degradation of two selected psychoactive drugs, amitriptyline (AMI) and alprazolam (ALP), under simulated solar and UV irradiation in an aqueous system. The newly synthesized photocatalysts were characterized using the following techniques: SEM/EDS, XRD, DLS, and UV/Vis spectroscopy. The obtained data confirmed the successful synthesis and the possible photocatalytic application of the new materials. Concerning the photocatalytic evaluation, the main results indicate that the highest removal efficiency of AMI and ALP was reached in the presence of ZnO/SnO₂ synthesized in a molar ratio of 2:1 and calcined at 700 °C, under 1.0 mg/mL catalyst loading. Based on the reutilization findings, it can be concluded that the mentioned photocatalyst had not lost its efficiency after three successive runs for the photodegradation of ALP. Additionally, pure ZnO powders showed the highest activity after calcination at 500 °C, in the case of both examined pollutants. The experiments with tert-butanol, sodium fluoride, and ethylenediaminetetraacetic acid suggested that the relative contribution of various reactive species changed in the following order: positively charged holes > ${\mathrm{OH}}_{\mathrm{free}}^{•}$ > ${\mathrm{OH}}_{\mathrm{ads}}^{•}$.