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TiO 2 -SiO 2 thin films were created on Corning glass substrates using a simple method. Nine layers of SiO 2 were deposited; later, several layers of TiO 2 were deposited, and their influence was studied. Raman spectroscopy, high resolution transmission electron spectroscopy (HRTEM), an X-ray diffractometer (XRD), ultraviolet-visible spectroscopy (UV-Vis), a scanning electron microscope (SEM), and atomic force microscopy (AFM) were used to describe the sample's shape, size, composition, and optical characteristics. Photocatalysis was realized through an experiment involving the deterioration of methylene blue (MB) solution exposed to UV-Vis radiation. With the increase of TiO 2 layers, the photocatalytic activity (PA) of the thin films showed an increasing trend, and the maximum degradation efficiency of MB by TiO 2 -SiO 2 was 98%, which was significantly higher than that obtained by SiO 2 thin films. It was found that an anatase structure was formed at a calcination temperature of 550 °C; phases of brookite or rutile were not observed. Each nanoparticle's size was 13-18 nm. Due to photo-excitation occurring in both the SiO 2 and the TiO 2 , deep UV light (λ = 232 nm) had to be used as a light source to increase photocatalytic activity.

Industrial expansion and increased water consumption have created water scarcity concerns. Meanwhile, conventional wastewater purification methods have failed to degrade recalcitrant pollutants efficiently. The present review paper discusses the recent advances and challenges in photocatalytic processes applied for industrial effluents treatment, with respect to phenolic compounds degradation. Key operational parameters including the catalyst loading, light intensity, initial pollutants concentration, pH, and type and concentrations of oxidants are evaluated and discussed. Compared to the other examined controlling parameters, pH has the highest effect on the photo-oxidation of contaminants by means of the photocatalyst ionization degree and surface charge. Furthermore, major phenolic compounds derived from industrial sources are comprehensively presented and the applicability of photocatalytic processes and the barriers in practical applications, including high energy demand, technical challenges, photocatalyst stability, and recyclability have been explored. The importance of energy consumption and operational costs for realistic large-scale processes are also discussed. Finally, research gaps in this area and the suggested direction for improving degradation efficiencies in industrial applications are presented. In the light of these premises, selective degradation processes in real water matrices such as untreated sewage are proposed., (Copyright © 2022. Published by Elsevier Ltd.)

The application of TiO 2 as a slurry catalyst for the degradation of contaminants of emerging concern (CEC) in liquid effluents has some drawbacks due to the difficulties in the catalyst reutilization. Thus, sophisticated and expensive separation methods are required after the reaction step. Alternatively, several types of materials have been used to support powder catalysts, so that fixed or fluidized bed reactors may be used. In this context, the objective of this work is to systematize and analyze the results of research inherent to the application of ceramic materials as support of TiO 2 in the photocatalytic CEC removal from liquid effluents. Firstly, an overview is given about the treatment processes able to degrade CEC. In particular, the photocatalysts supported in ceramic materials are analyzed, namely the immobilization techniques applied to support TiO 2 in these materials. Finally, a critical review of the literature dedicated to photocatalysis with supported TiO 2 is presented, where the performance of the catalyst is considered as well as the main drivers and barriers for implementing this process. A focal point in the future is to investigate the possibility of depurating effluents and promote water reuse in safe conditions, and the supported TiO 2 in ceramic materials may play a role in this scope.

ZnO/Fe 2 O 3 /Clinoptilolite photocatalyst was synthesized through sol-gel method. The photocatalyst was characterized by XRD, XRF, EDX, FE-SEM, FT-IR, BET and UV-VIS DRS analyses. According to the XRD, FT-IR, and EDX results, the presence of ZnO and Fe 2 O 3 was confirmed on the clinoptilolite surface. Based on the XRF results, the molar ratio of Fe 3+ /ZnO in the photocatalyst was obtained as 0.06. The FE-SEM results confirmed stabilization of ZnO/Fe 2 O 3 on the clinoptilolite surface. Based on the BET results, the surface area and pore volume for the photocatalyst were obtained as 291.35 m 2 /g and 0.23 cm 3 /g, respectively. According to the UV-VIS DRS results, the band gap energy of the photocatalyst was measured as 3.38 eV. The performance of the synthesized photocatalyst in degrading metronidazole from contaminated water, as one of the most widely used antibiotics in pharmaceutical industries, was evaluated by response surface methodology. Operational factors including pH (4-10), metronidazole concentration (1-100 mg/l), irradiation time (45-180 min), photocatalyst concentration (0.5-2 g/l), and H 2 O 2 concentration (25-100 mg/l) were investigated. The optimal values of the factors in degrading 99% of the contaminant were as follows: irradiation time = 90 min, photocatalyst concentration = 1 g/l, pH = 10, H 2 O 2 concentration = 40 mg/l, and MNZ concentration = 60 mg/l.

The implementation of heterogeneous photo-nanocatalysts in organic syntheses has been investigated greatly in the last decade as a result of the increasing demand to achieve the organic reactions via the use of green approaches and through the availability of visible light source. Herein, the presented results describe the basic concepts and state-of-the-art of fundamental insight into key features that influence the catalytic performance in organic reactions to investigate and optimize a broad range of catalyzed organic transformations, that benefit the researchers in academia and chemical industry fields., (Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.)

Perfluorochemicals (PFCs) are a set of chemicals containing C-F bonds, which are concerned due to their bioaccumulation property, persistent and toxicological properties. Photocatalytic approaches have been widely studied for the effective removal of PFCs due to the mild operation conditions. This review aims to provide a comprehensive and up-to-date summary on the homogenous and heterogeneous photocatalytic processes for PFCs removal. Specifically, the homogenous photocatalytic methods for remediating PFCs are firstly discussed, including generation of hydrated electrons (e aq ) and its performance and mechanisms for photo-reductive destruction of PFCs, the active species responsible for photo-oxidative degradation of PFCs and the corresponding mechanisms, and metal-ion-mediated (Fe(III) mainly used) processes for the remediation of PFCs. The influences of molecular structures of PFCs and water matrix, such as dissolved oxygen, humic acid, nitrate, chloride on the homogenous photocatalytic degradation of PFCs are also discussed. For heterogeneous photocatalytic processes, various semiconductor photocatalysts used for the decomposition of perfluorooctanoic acid (PFOA) are then discussed in terms of their specific properties benefiting photocatalytic performances. The preparation methods for optimizing the performance of photocatalysts are also overviewed. Moreover, the photo-oxidative and photo-reductive pathways are summarized for remediating PFOA in the presences of different semiconductor photocatalysts, including active species responsible for the degradation. We finally put forward several key perspectives for the photocatalytic removal of PFCs to promote its practical application in PFCs-containing wastewater treatment, including the treatment of PFCs degradation products such as fluoride ion, and the development of noble-metal free photocatalysts that could efficiently remove PFCs under solar light irradiation.‒ ) and its performance and mechanisms for photo-reductive destruction of PFCs, the active species responsible for photo-oxidative degradation of PFCs and the corresponding mechanisms, and metal-ion-mediated (Fe(III) mainly used) processes for the remediation of PFCs. The influences of molecular structures of PFCs and water matrix, such as dissolved oxygen, humic acid, nitrate, chloride on the homogenous photocatalytic degradation of PFCs are also discussed. For heterogeneous photocatalytic processes, various semiconductor photocatalysts used for the decomposition of perfluorooctanoic acid (PFOA) are then discussed in terms of their specific properties benefiting photocatalytic performances. The preparation methods for optimizing the performance of photocatalysts are also overviewed. Moreover, the photo-oxidative and photo-reductive pathways are summarized for remediating PFOA in the presences of different semiconductor photocatalysts, including active species responsible for the degradation. We finally put forward several key perspectives for the photocatalytic removal of PFCs to promote its practical application in PFCs-containing wastewater treatment, including the treatment of PFCs degradation products such as fluoride ion, and the development of noble-metal free photocatalysts that could efficiently remove PFCs under solar light irradiation., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2020 Elsevier Ltd. All rights reserved.)

The severe energy crisis and environmental issues have led to an increase in research on the development of sustainable energy. Atomically thin 2D multinary nanosheets with tunable components show advantages for producing sustainable energy via photo, electrocatalysis processes. Here, recent progress of atomically thin 2D multinary nanosheets from the design, synthesis, tuning, and sustainable energy production via photo, electrocatalysis processes is summarized. The regulating strategies such as alloying, doping, vacancy engineering, pores construction, surface modification, and heterojunction are summarized, focusing on how to optimize the catalytic performance of atomically thin 2D multinary nanosheets. In addition, advancements in versatile energy-related photo, electrocatalytic applications in the areas of oxygen evolution, oxygen reduction, hydrogen evolution, CO 2 reduction, and nitrogen fixation are discussed. Finally, existing challenges and future research directions in this promising field are presented.

The aim of the present work was to experimentally evaluate an alternative advanced wastewater treatment system, which combines the action of photocatalytic oxidation with ceramic membrane filtration. Experiments were carried out using laboratory scale TiO 2 /UV photocatalytic reactor and tubular ceramic microfiltration (CMF) system to treat the secondary effluent (SE). A 100-nm pore size CMF membrane was investigated in cross flow mode under constant transmembrane pressure of 20 kPa. The results show that specific flux decline of CMF membrane with and without TiO 2 /UV photocatalytic treatment was 30 and 50%, respectively, after 60 min of filtration. Data evaluation revealed that the adsorption of organic compounds onto the TiO 2 particles was dependent on the pH of the suspension and was considerably higher at low pH. The liquid chromatography-organic carbon detector (LC-OCD) technique was used to characterise the dissolved organic matter (DOM) present in the SE and was monitored following photocatalysis and CMF. The results showed that there was no removal of biopolymers and slight removal of humics, building blocks and the other oxidation by-products after TiO 2 /UV photocatalytic treatment. This result suggested that the various ions present in the SE act as scavengers, which considerably decrease the efficiency of the photocatalytic oxidation reactions. On the other hand, the CMF was effective for removing 50% of biopolymers with no further removal of other organic components after photocatalytic treatment. Thus, the quantity of biopolymers in SE has an apparent correlation with the filterability of water samples in CMF.